SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12673736 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43558170 | GAACAAGAGCTCAAA[G/T]GAGGACAGAGGAAAG | 23072 |
rs12673745 | snp | C/T | 0.20111 | 0.245173 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359076 | AATGATCCACCCACC[C/T]CGGCCTCCCAAAGTG | 23072 |
rs12673816 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156795 | TGATGTGTGTTACCT[C/T]TAGGTTGAAGTTTAT | 23072 |
rs12673835 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302358 | CAGCTGCCCTTCTCA[G/T]GCTTCAGCTTCCCGG | 23072 |
rs12674134 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43232964 | AATATTCTGATTACT[A/G]TGTTTAGTTGTAGAG | 23072 |
rs12674179 | snp | G/T | 0.199873 | 0.244923 | intron-variant | HECW1 | GRCh38.p7 | 7:43173007 | CTCTCCAAAGCAGTG[G/T]TTTCACACCACATTG | 23072 |
rs12690832 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134011 | AGCTGTGTCCATCTT[C/T]GGAAAATATAATTAG | 23072 |
rs12702015 | snp | G/T | 0.495878 | 0.0452105 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150880 | AGGACTTCAGCATCT[G/T]TATCAGCGCCCCCCC | 23072 |
rs12702020 | snp | G/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43184204 | atttttagtagagac[G/T]gggtttcactgtgtt | 23072 |
rs12702021 | snp | C/T | 0.333722 | 0.235565 | intron-variant | HECW1 | GRCh38.p7 | 7:43184307 | cgtgagccaccgccc[C/T]gccaattcttacatt | 23072 |
rs12702022 | snp | C/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43187150 | TGTTTTCCTTGCTAC[C/G]TGGACCTCTCCATAG | 23072 |
rs12702023 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43188529 | TGAGAATACTGTCTC[A/G]GTCAGCACTGACTAG | 23072 |
rs12702025 | snp | A/G | 0.497722 | 0.0336691 | intron-variant | HECW1 | GRCh38.p7 | 7:43222877 | TGGTCATCCCATCCC[A/G]TCTTATGACCTATTT | 23072 |
rs12702026 | snp | A/G | 0.498754 | 0.0249289 | intron-variant | HECW1 | GRCh38.p7 | 7:43226889 | GCGTGTGGGGGCTCC[A/G]GAACACAGGATGGGG | 23072 |
rs12702027 | snp | A/G | 0.498437 | 0.0279115 | intron-variant | HECW1 | GRCh38.p7 | 7:43227217 | AACATTGATCTTGAA[A/G]TTCAGGCTACTGAAA | 23072 |
rs12702028 | snp | C/T | 0.421842 | 0.181577 | intron-variant | HECW1 | GRCh38.p7 | 7:43237647 | GATGAGCATTTACCA[C/T]TGTATCTGCAGCTCC | 23072 |
rs12702030 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335983 | tccctctctctctct[C/T]tctctctctctcctt | 23072 |
rs12702031 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335985 | cctctctctctcttt[C/T]tctctctctccttcc | 23072 |
rs12702032 | snp | A/T | 0.0551013 | 0.156571 | intron-variant | HECW1 | GRCh38.p7 | 7:43346531 | ctttgtttttattgc[A/T]tttgcttttgggttc | 23072 |
rs12702033 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | HECW1 | GRCh38.p7 | 7:43352662 | aaaataagaatgaca[G/T]GTGacatttactgag | 23072 |
rs12702034 | snp | A/G | 0.164546 | 0.234942 | intron-variant | HECW1 | GRCh38.p7 | 7:43354023 | tttgggacctcctcc[A/G]ttcaggatgggcagc | 23072 |
rs12702035 | snp | A/G | 0.16911 | 0.236552 | intron-variant | HECW1 | GRCh38.p7 | 7:43354259 | caaagacatagctgt[A/G]tatctacaagaaaaa | 23072 |
rs12702037 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43354815 | gatacagaaagatca[G/T]agaacaccaaacaga | 23072 |
rs12702038 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | HECW1 | GRCh38.p7 | 7:43366635 | TAAATGGTCTTGAGC[C/G]CTTGTGCTTGGCAGA | 23072 |
rs12702039 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | HECW1 | GRCh38.p7 | 7:43378971 | CAGACATAGAACATG[C/G]GGTGGTTATTGCTTA | 23072 |
rs12702040 | snp | A/G | 0.40263 | 0.198 | intron-variant | HECW1 | GRCh38.p7 | 7:43387952 | TTAGCCTGATTTAGA[A/G]CATGTATTATGTGAC | 23072 |
rs12702041 | snp | A/G | 0.100588 | 0.200439 | intron-variant | HECW1 | GRCh38.p7 | 7:43406111 | attcctgcctgttct[A/G]gagggctgcctttca | 23072 |
rs12702042 | snp | A/G | 0.282369 | 0.247896 | intron-variant | HECW1 | GRCh38.p7 | 7:43427212 | ATAACAGTTTCCCCA[A/G]CTATGATCAATATAA | 23072 |
rs12702043 | snp | A/G | 0.197703 | 0.244469 | intron-variant | HECW1 | GRCh38.p7 | 7:43441857 | CAACCACACAAAAAC[A/G]GGTGGTGGGCCACAT | 23072 |
rs12702044 | snp | A/G | 0.273318 | 0.24891 | intron-variant | HECW1 | GRCh38.p7 | 7:43459447 | ATCAACTGAAGTTTT[A/G]TTTTTTAATTATTTG | 23072 |
rs12702045 | snp | A/C | 0.332337 | 0.236052 | intron-variant | HECW1 | GRCh38.p7 | 7:43468090 | TGTCCTTTCACCACC[A/C]GCCCCCACCACACAC | 23072 |
rs12702046 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | HECW1 | GRCh38.p7 | 7:43481630 | AGTTAATTTAATATC[A/C]TTTAAATCATTAATA | 23072 |
rs12702049 | snp | C/T | 0.364401 | 0.222289 | intron-variant | HECW1 | GRCh38.p7 | 7:43548679 | gagtgtggtggtcca[C/T]gcctataatcctagc | 23072 |
rs12702050 | snp | A/G | 0.421842 | 0.181577 | intron-variant | HECW1 | GRCh38.p7 | 7:43559655 | ACTAGACCGGGGTCA[A/G]CATAGAAGTCTTCCA | 23072 |
rs12702051 | snp | C/T | 0.421051 | 0.182323 | intron-variant | HECW1 | GRCh38.p7 | 7:43559889 | TAAATGCAATAAAAG[C/T]AACTAGTAAGTAAAC | 23072 |
rs13222216 | snp | A/C | 0.498369 | 0.0285077 | intron-variant | HECW1 | GRCh38.p7 | 7:43446814 | CATGGAAAGGTACCC[A/C]CAAGGAGCGGGATGG | 23072 |
rs13222627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139013 | TGTTTGTTTTAATAA[C/T]ATTTAGTATTTTAGC | 23072 |
rs13222817 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43352064 | CTTCTCAGCCTCTCA[A/G/T]ATGCTTCTTTTAGAA | 23072 |
rs13223787 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43418569 | tcttcaattttactg[G/T]atgttttctctataa | 23072 |
rs13223875 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43418600 | actccattctactat[C/G/T]gcttctatgcaatga | 23072 |
rs13223926 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43374954 | AGAAAATTTGTAGAC[A/C]CATAAATAAGAAAAA | 23072 |
rs13223934 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43374970 | CATAAATAAGAAAAA[A/C]CAATAATAATCCAAT | 23072 |
rs13224088 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43374803 | aaaaaaaaaaaaaTA[A/G]AGAAATATAATAACC | 23072 |
rs13224667 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348352 | tttctgtggtatcag[G/T]tgtaatatctcctgt | 23072 |
rs13225042 | snp | A/G | 0.32153 | 0.239548 | intron-variant | HECW1 | GRCh38.p7 | 7:43540546 | ATCTGGAGGTGGCCA[A/G]ATCTGTATGGCCAGT | 23072 |
rs13225071 | snp | A/C | 0.294576 | 0.245994 | intron-variant | HECW1 | GRCh38.p7 | 7:43216991 | CTTGCACCAGAGGGA[A/C]CAGCTGTCAAGGGTT | 23072 |
rs13225271 | snp | A/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43383723 | tgaacaacacaggag[A/T]ttagggcttccaatc | 23072 |
rs13226333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248747 | ctcctccttctcctg[C/T]ccctcttcccccatc | 23072 |
rs13226386 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | HECW1 | GRCh38.p7 | 7:43528505 | AAATATCACACTTTC[A/G]AATGATCAGTTTTAC | 23072 |
rs13226388 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43401586 | TTTTTTTTTTTTTTT[C/T]CCCCCAAATATAGCC | 23072 |
rs13226528 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506047 | AAAGGTATATATAGT[A/G]AAGTATTTACAAAGC | 23072 |
rs13226861 | snp | A/G | 0.415399 | 0.187465 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134508 | TTTATGTTTAAATTT[A/G]AATTTAAttttttta | 23072 |
rs13226955 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134375 | ctccagtgtgggtaa[A/G]agagtgagactctgt | 23072 |
rs13227224 | snp | A/T | 0.104504 | 0.2033 | intron-variant | HECW1 | GRCh38.p7 | 7:43398302 | aaGTTTAAAAGAAAA[A/T]CTGAGCTGCTCTGGC | 23072 |
rs13228569 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247899 | gggagggagagagga[A/G]ggaaggaaggaggga | 23072 |
rs13228648 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247738 | gaaggaagaaaggaa[A/G]gaaggagggagggag | 23072 |
rs13228745 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247800 | aaaagaaaagaagga[A/G]ggaaggaaagaaAAG | 23072 |
rs13229419 | snp | A/G | 0.166832 | 0.235761 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359108 | tgggattacaggcgt[A/G]agccaccgtgcccgg | 23072 |
rs13231695 | snp | A/G | 0.0486741 | 0.148216 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376739 | ggcgtggtggcaggc[A/G]tctgtaatcccagct | 23072 |
rs13232367 | snp | A/C | 0.369142 | 0.219784 | intron-variant | HECW1 | GRCh38.p7 | 7:43336611 | taagggtattacatg[A/C]ataataatgaggatt | 23072 |
rs13232385 | snp | C/G | 0.0221141 | 0.102801 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512297 | GAAGGACAGAGGTGC[C/G]TTAATGGACACCCAC | 23072 |
rs13233190 | snp | C/T | 0.442113 | 0.159977 | intron-variant | HECW1 | GRCh38.p7 | 7:43425150 | GCAATGGAGTTGCAA[C/T]AAGCTTTCAAGCCCA | 23072 |
rs13233479 | snp | C/G | 0.165527 | 0.235296 | intron-variant | HECW1 | GRCh38.p7 | 7:43395113 | caaacactgatctca[C/G]gagcaatttagggag | 23072 |
rs13234175 | snp | A/C | 0.224116 | 0.248656 | intron-variant | HECW1 | GRCh38.p7 | 7:43537961 | ACCCCGTCGCCACAC[A/C]CCCTGGTTGAGAGGC | 23072 |
rs13234419 | snp | C/T | 0.273856 | 0.248859 | intron-variant | HECW1 | GRCh38.p7 | 7:43538116 | CTGAGTTAGAACAGT[C/T]AGAGAATCATGCTGA | 23072 |
rs13235306 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488407 | aaggaaggaaatgaa[A/G]gaaagagagagagag | 23072 |
rs13235578 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488418 | tgaaagaaagagaga[A/G]agagaaagaaagaaa | 23072 |
rs13236014 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | HECW1 | GRCh38.p7 | 7:43337409 | agttgtttgagtcat[C/G]tgatatagactcATC | 23072 |
rs13236084 | snp | A/G | 0.162909 | 0.23434 | intron-variant | HECW1 | GRCh38.p7 | 7:43370949 | ctggagtgcagtggc[A/G]caatctcggcccact | 23072 |
rs13236556 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43418455 | ttctctccccttttt[C/T]ttgagctccaaatga | 23072 |
rs13236774 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43418593 | tctataaactccatt[A/C]tactattgcttctat | 23072 |
rs13236782 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43418602 | tccattctactattg[C/G]ttctatgcaatgaat | 23072 |
rs13236847 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43418492 | tgctagatcttcaga[G/T]tcccacaggtccctg | 23072 |
rs13237872 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43221538 | GTCAGAGGAATTAGG[G/T]TTTTTTTTTTTtttt | 23072 |
rs13237907 | snp | A/G | 0.174932 | 0.238463 | intron-variant | HECW1 | GRCh38.p7 | 7:43200473 | aaacccggcagccaa[A/G]tcagatttcttctct | 23072 |
rs13238271 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43383722 | ttgaacaacacagga[A/G]tttagggcttccaat | 23072 |
rs13238354 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43374801 | aaaaaaaaaaaaaaa[A/T]aGAGAAATATAATAA | 23072 |
rs13238388 | snp | A/G | 0.411914 | 0.190483 | intron-variant | HECW1 | GRCh38.p7 | 7:43471894 | TTTTTTTCAGAAAGT[A/G]TATTTTTTTCCCAGA | 23072 |
rs13238475 | snp | C/T | 0.269267 | 0.249256 | intron-variant | HECW1 | GRCh38.p7 | 7:43405067 | aaccagccctgacaa[C/T]ctgtaagccttcatt | 23072 |
rs13238604 | snp | A/G | 0.173965 | 0.238157 | intron-variant | HECW1 | GRCh38.p7 | 7:43349162 | gcctcagcctaccga[A/G]tagttgggattacag | 23072 |
rs13239072 | snp | A/G | 0.275197 | 0.248727 | intron-variant | HECW1 | GRCh38.p7 | 7:43526745 | GTGGCTCACGCCTGT[A/G]ATCCCAACACTTTGG | 23072 |
rs13239156 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248710 | tttcctcctcctcct[C/T]ctcctcctcctcctc | 23072 |
rs13239158 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248716 | cctcctcctcctcct[C/G]ctcctcctccttttc | 23072 |
rs13239169 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248748 | tcctccttctcctgt[C/T]cctcttcccccatct | 23072 |
rs13239366 | snp | C/T | 0.32153 | 0.239548 | intron-variant | HECW1 | GRCh38.p7 | 7:43540621 | TTTTAAAGAGTGATG[C/T]TCATTCAGCTTATCT | 23072 |
rs13239877 | snp | A/T | 0.1652 | 0.235179 | intron-variant | HECW1 | GRCh38.p7 | 7:43396296 | CGAGGAAGGCAATTG[A/T]TTAATTAAGAGAGAC | 23072 |
rs13240079 | snp | A/G | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125780 | aaaaaaaaaaaaaaa[A/G]GAGTGAGGCATTAAT | 23072 |
rs13240559 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | HECW1 | GRCh38.p7 | 7:43362083 | gtgcagtgagcagag[A/G]tcgcaccactgcact | 23072 |
rs13241883 | snp | A/G | 0.350764 | 0.228794 | intron-variant | HECW1 | GRCh38.p7 | 7:43472471 | CAAGGGCCAAGAATC[A/G]TGCCTAGTATATAGT | 23072 |
rs13242832 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43196551 | AGGTCCCGGCTCTCA[A/G]AGGGTAACTGCATAT | 23072 |
rs13242934 | snp | A/G | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131638 | AATGTGGCTTTTCAG[A/G]AAAGTTGTAACAACA | 23072 |
rs13243191 | snp | A/G | 0.199655 | 0.244878 | intron-variant | HECW1 | GRCh38.p7 | 7:43550630 | GGCAAGCTGTGGCCA[A/G]GGTGCTGCTTCACGG | 23072 |
rs13243213 | snp | A/G | 0.47614 | 0.106587 | intron-variant | HECW1 | GRCh38.p7 | 7:43226958 | CACGGCTGTCACAAC[A/G]TCATGAAAACTGCCT | 23072 |
rs13243703 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43181015 | tctcccctaacctcc[C/T]cagcctgtgataacc | 23072 |
rs13243945 | snp | A/C | 0.286042 | 0.247388 | intron-variant | HECW1 | GRCh38.p7 | 7:43545549 | ACTTTTGATTTTCCA[A/C]AAACTTAACTACTGG | 23072 |
rs13244563 | snp | C/G/T | 0.00934559 | 0.067716 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127245 | aaacaaacagctggc[C/G/T]gggcaaggtagctca | 23072 |
rs13245248 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158439 | CATTATCTCAAGATC[C/T]GGACATAACTACTGT | 23072 |
rs13245386 | snp | A/G | 0.254944 | 0.249951 | intron-variant | HECW1 | GRCh38.p7 | 7:43473412 | GATCACTAATGAATC[A/G]AAGCACGACATTAAT | 23072 |
rs13246170 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281966 | CTCTCTCCATGAGCC[C/T]TTTTCGAGTCCCTCA | 23072 |
rs13246765 | snp | C/T | 0.243061 | 0.249904 | intron-variant | HECW1 | GRCh38.p7 | 7:43345801 | tccatcatatatata[C/T]acacacacacacaca | 23072 |
rs13246891 | snp | C/T | 0.173643 | 0.238054 | intron-variant | HECW1 | GRCh38.p7 | 7:43190682 | GAGAAATGCTCTAAC[C/T]ATCCCAAATGGGGCA | 23072 |
rs13247140 | snp | A/G | 0.229429 | 0.249152 | intron-variant | HECW1 | GRCh38.p7 | 7:43345920 | ttgggttgcttgcac[A/G]attttgcaattgtga | 23072 |
rs13307381 | snp | A/G | 0.166832 | 0.235761 | intron-variant | HECW1 | GRCh38.p7 | 7:43488494 | agaaagaaagagaaa[A/G]aaagaaagaaaAGAA | 23072 |
rs13437775 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328309 | tctcaaattaaaaac[A/G]aaaaacaaaaaacaa | 23072 |
rs13437856 | snp | A/G | 0.359152 | 0.224913 | intron-variant | HECW1 | GRCh38.p7 | 7:43400097 | AAAAGTTAGCCAGCC[A/G]TGGTGGCATGTACCT | 23072 |
rs13438260 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134195 | ggtcaggagttccag[A/C]ccagcctggccaaca | 23072 |
rs13438437 | snp | G/T | 0.303187 | 0.244277 | intron-variant | HECW1 | GRCh38.p7 | 7:43400102 | TTAGCCAGCCATGGT[G/T]GCATGTACCTATAGT | 23072 |
rs13438792 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43273399 | GACAGATTAGTGGAA[A/C]TATATAAATTGAACA | 23072 |
rs17151028 | snp | A/G | 0.45889 | 0.13735 | intron-variant | HECW1 | GRCh38.p7 | 7:43504908 | AAAGGAGGTGTCCTC[A/G]CTAAGGTCGCCATGA | 23072 |
rs17172162 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132326 | ATCTTCAGATGTCTC[C/T]ATCAAAAAGTACAAT | 23072 |
rs17172164 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133098 | TGACCTAATGAAATG[A/G]TCAATTACATTAATA | 23072 |
rs17172166 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136715 | TTTTGCAATCCAACC[C/G]ATCCAAACTGCAGAT | 23072 |
rs17172168 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153226 | AATATATGGATTGTT[G/T]CATTGTCATTATTTC | 23072 |
rs17172169 | snp | C/T | 0.117537 | 0.212022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158873 | TAGGACCCTGACTTA[C/T]GCACCAAGAGAGAGG | 23072 |
rs17172171 | snp | C/T | 0.162581 | 0.234218 | intron-variant | HECW1 | GRCh38.p7 | 7:43190905 | TATCAAATCCCAAAC[C/T]GGAGTCTGTCTCAAG | 23072 |
rs17172172 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43197386 | ATCAGAGAAAGGCTC[C/T]GCTGCCCTAGACCAC | 23072 |
rs17172173 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | HECW1 | GRCh38.p7 | 7:43206175 | ACTTTTAGATGAGCT[C/G]CTACCATGTGCACTC | 23072 |
rs17172174 | snp | A/G | 0.307176 | 0.243374 | intron-variant | HECW1 | GRCh38.p7 | 7:43215917 | GGACGTATAGGGCCA[A/G]TGTTCAGAGACCAGG | 23072 |
rs17172175 | snp | A/G | 0.281841 | 0.247964 | intron-variant | HECW1 | GRCh38.p7 | 7:43226786 | AAAATGCTGCCCTCC[A/G]AAGAGCCTGGCGTCT | 23072 |
rs17172176 | snp | A/G | 0.153665 | 0.230694 | intron-variant | HECW1 | GRCh38.p7 | 7:43240535 | TATGGTCTGAAGGGT[A/G]ACGTGCTTTCTAATA | 23072 |
rs17172177 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | HECW1 | GRCh38.p7 | 7:43241184 | GCAGAAGCAAGGGGC[C/T]GTGCAGATCTGTGTA | 23072 |
rs17172178 | snp | C/G | 0.186421 | 0.24178 | intron-variant | HECW1 | GRCh38.p7 | 7:43241324 | TTCCTGATGAAAGAG[C/G]GTTCCATCCAGGTTC | 23072 |
rs17172179 | snp | A/T | 0.251578 | 0.249995 | intron-variant | HECW1 | GRCh38.p7 | 7:43241541 | CGGTATCCCCAGTAC[A/T]AAGTGCTAAATAGAT | 23072 |
rs17172180 | snp | C/T | 0.152334 | 0.230133 | intron-variant | HECW1 | GRCh38.p7 | 7:43243207 | TTAAGAGGGCCCTGA[C/T]AGATGATGCCGTCAG | 23072 |
rs17172181 | snp | A/C | 0.416218 | 0.186739 | intron-variant | HECW1 | GRCh38.p7 | 7:43243516 | TGTGAGGATGCTTTT[A/C]GCTGGCCTTCTCAGA | 23072 |
rs17172182 | snp | C/G | 0.4087 | 0.193169 | intron-variant | HECW1 | GRCh38.p7 | 7:43245999 | AAGATTCATCATGCT[C/G]TGAAATGAGTCTGCA | 23072 |
rs17172183 | snp | C/G | 0.407845 | 0.193868 | intron-variant | HECW1 | GRCh38.p7 | 7:43246025 | CTGCAGCACTACTAG[C/G]TGGACTTATGAAAAT | 23072 |
rs17172184 | snp | A/G | 0.476833 | 0.105105 | intron-variant | HECW1 | GRCh38.p7 | 7:43246530 | AAAAGGTCTCTAGGT[A/G]ATTCTGGTATGCACT | 23072 |
rs17172185 | snp | C/T | 0.294832 | 0.245947 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247240 | ACAATGGAAGAAATA[C/T]GCAGGAAAACTTGGT | 23072 |
rs17172187 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43267709 | GCTAATTAAGAGAAA[A/G]CAAATATTCATGATT | 23072 |
rs17172188 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | HECW1 | GRCh38.p7 | 7:43274959 | GAAGATGTCCTGAGA[C/T]GGGCACTCAGTGCAG | 23072 |
rs17172189 | snp | C/T | 0.249603 | 0.25 | intron-variant | HECW1 | GRCh38.p7 | 7:43276745 | TGACGATTTATAGTA[C/T]GTACAAAATTAGCTC | 23072 |
rs17172190 | snp | A/G | 0.084364 | 0.187256 | intron-variant | HECW1 | GRCh38.p7 | 7:43279502 | AACCCGACCATCCAC[A/G]CTCTTCTTTTTTACT | 23072 |
rs17172192 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | HECW1 | GRCh38.p7 | 7:43290696 | ACAGGGACGTCATAA[C/T]GTCCAGAGCCCCAGT | 23072 |
rs17172193 | snp | C/T | 0.0850919 | 0.187897 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295965 | GATATTTTCATTGGC[C/T]CATGGTCATGCCTGC | 23072 |
rs17172194 | snp | A/G | 0.0803491 | 0.183626 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297082 | ATCTCCAGGAAGAAG[A/G]CTGTTTTATTTTTAA | 23072 |
rs17172195 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43314757 | AATAACTTCCAAATC[C/T]GAAATTGTCTGTGAA | 23072 |
rs17172196 | snp | C/T | 0.227664 | 0.249 | intron-variant | HECW1 | GRCh38.p7 | 7:43327702 | GTAGAGGAAGGAGCC[C/T]AAGCTACCAAGTCCA | 23072 |
rs17172197 | snp | C/G | 0.38286 | 0.211774 | intron-variant | HECW1 | GRCh38.p7 | 7:43333674 | CATGAGACTTATGCT[C/G]AAGGACAGCAGCCAT | 23072 |
rs17172198 | snp | C/T | 0.382666 | 0.211895 | intron-variant | HECW1 | GRCh38.p7 | 7:43334049 | ATTCCTACGTTATAC[C/T]TCTCTCTTTTAACCT | 23072 |
rs17172199 | snp | A/C | 0.0839998 | 0.186933 | intron-variant | HECW1 | GRCh38.p7 | 7:43337677 | TCTCAGTGTCTTCAG[A/C]TGCTCTTGCTGGATG | 23072 |
rs17172202 | snp | C/T | 0.228547 | 0.249078 | intron-variant | HECW1 | GRCh38.p7 | 7:43358101 | TGCCCGTTTGGGATT[C/T]CTGGTACCTAAAATT | 23072 |
rs17172203 | snp | C/T | 0.228842 | 0.249103 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358536 | TGGTTAGCATCCAGG[C/T]ATCACCCAGGTAATG | 23072 |
rs17172204 | snp | A/G | 0.200492 | 0.245049 | intron-variant | HECW1 | GRCh38.p7 | 7:43363770 | AAAGCTGTTTATCAC[A/G]CATTATTCTAGTTGA | 23072 |
rs17172206 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | HECW1 | GRCh38.p7 | 7:43403755 | GTATGTTCTCAACTA[C/T]GCAAAGAAAAATACT | 23072 |
rs17172209 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43447285 | ATCTACACATGGTCA[A/G]TTGAAACTTGGCTCA | 23072 |
rs17172210 | snp | A/T | 0.233235 | 0.249437 | intron-variant | HECW1 | GRCh38.p7 | 7:43456694 | CTTAATAGCCTAGGC[A/T]CAAAAATAGGAGTTT | 23072 |
rs17172215 | snp | A/G | 0.399611 | 0.200291 | intron-variant | HECW1 | GRCh38.p7 | 7:43497555 | ACAGATGCAATGTTT[A/G]GGCAGCTCTGTGGGG | 23072 |
rs17172216 | snp | A/G | 0.170084 | 0.236883 | intron-variant | HECW1 | GRCh38.p7 | 7:43500509 | TACCTGTGCAAGTCT[A/G]TAGAAAAGCCATCCC | 23072 |
rs17172217 | snp | C/G | 0.131723 | 0.220251 | intron-variant | HECW1 | GRCh38.p7 | 7:43503822 | GACAGGTGATAGTAC[C/G]AGCGGTAGTGAAAAT | 23072 |
rs17172218 | snp | A/G | 0.154993 | 0.231244 | intron-variant | HECW1 | GRCh38.p7 | 7:43506298 | TTTCAATCACTTCTT[A/G]TAGCAACTTACAAGA | 23072 |
rs17172219 | snp | A/G | 0.00321186 | 0.0399451 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43508093 | GCGGAAAGAGCTCCA[A/G]CGAAACAAGCTCTAC | 23072 |
rs17172220 | snp | G/T | 0.299664 | 0.245017 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509643 | CTATTACCACTTACC[G/T]ATATGTATAAGAAGA | 23072 |
rs17172222 | snp | C/T | 0.26271 | 0.249677 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522268 | TTTAGTTTTCAAATG[C/T]TGGCAACTGAAGAAC | 23072 |
rs17172223 | snp | A/G | 0.404035 | 0.196909 | intron-variant | HECW1 | GRCh38.p7 | 7:43526667 | GCTCAAATAATTAAG[A/G]CTTCTAAACCTTCAC | 23072 |
rs17172224 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | HECW1 | GRCh38.p7 | 7:43527080 | ATGGTCAAATTTTCT[A/G]TATAATTCTGGGCTT | 23072 |
rs17172226 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | HECW1 | GRCh38.p7 | 7:43550893 | TAGCATCTCTTGTCA[C/T]AATATATGCAGCTGG | 23072 |
rs17172227 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43556093 | ACTAATCACAGCACA[A/G]GGTAGAATCAGAGGA | 23072 |
rs17172228 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | HECW1 | GRCh38.p7 | 7:43557353 | TTCCCAGATGAGAGC[A/G]CCAGACACCGCCACA | 23072 |
rs17206734 | snp | A/T | 0.193028 | 0.243422 | intron-variant | HECW1 | GRCh38.p7 | 7:43392085 | AATGATATTTTCACC[A/T]CATTTTTAGGTTCCA | 23072 |
rs17206894 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | HECW1 | GRCh38.p7 | 7:43398446 | ACTACCTTAGCTTGT[C/T]AAATCAACAGATGTT | 23072 |
rs17207007 | snp | A/C | 0.195526 | 0.243993 | intron-variant | HECW1 | GRCh38.p7 | 7:43406429 | ACCTTGGATCAACTC[A/C]AAATAACTTTTAAAT | 23072 |
rs17207421 | snp | A/G | 0.202651 | 0.245475 | intron-variant | HECW1 | GRCh38.p7 | 7:43435480 | TAATAGCAATCAGAC[A/G]TACCACATGGTCACT | 23072 |
rs17208350 | snp | A/G | 0.191147 | 0.242974 | intron-variant | HECW1 | GRCh38.p7 | 7:43495658 | CAAGTGATCTTTAGC[A/G]TGATGAATGGCCACT | 23072 |
rs17208513 | snp | C/T | 0.178785 | 0.239642 | intron-variant | HECW1 | GRCh38.p7 | 7:43500518 | AAGTCTGTAGAAAAG[C/T]CATCCCTCATAGAGC | 23072 |
rs17208534 | snp | C/T | 0.176861 | 0.239062 | intron-variant | HECW1 | GRCh38.p7 | 7:43502753 | GACTGGATCCAGATA[C/T]TGGAGAATTTTTCCA | 23072 |
rs17208701 | snp | A/G | 0.16618 | 0.23553 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508543 | CCCATGTAGGAAGGC[A/G]TATCAAAATGAACTT | 23072 |
rs17208834 | snp | A/C | 0.165853 | 0.235413 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510438 | CATCAGGAATACCTT[A/C]GCTAATTTAACAATT | 23072 |
rs17208856 | snp | C/T | 0.165527 | 0.235296 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510486 | TATGTTCTGGGAGGA[C/T]ACAAACATAAAATGA | 23072 |
rs17208912 | snp | A/G | 0.308661 | 0.24302 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515857 | CAAGTTAAAATGCTC[A/G]CATATTTTGAATGGA | 23072 |
rs17209031 | snp | C/T | 0.347473 | 0.230215 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517537 | GAACTTAAGAAGTCC[C/T]GGATAACACATTTTA | 23072 |
rs17209094 | snp | C/G | 0.170408 | 0.236992 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520020 | AAAATTACATCTGTG[C/G]GTAAAAAATAAATAA | 23072 |
rs17209297 | snp | A/G | 0.28052 | 0.24813 | intron-variant | HECW1 | GRCh38.p7 | 7:43524543 | TAATAGAACTTAGCA[A/G]TTATGAAGTACTTTT | 23072 |
rs17209332 | snp | A/G | 0.197393 | 0.244402 | intron-variant | HECW1 | GRCh38.p7 | 7:43525184 | CAAGCCCAATAATCG[A/G]TCGGAATATGTGGTC | 23072 |
rs17339479 | snp | A/C | 0.301416 | 0.244656 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43501288 | TAGCTTCTCTCCCCG[A/C]TGTTCACCCTGTTCT | 23072 |
rs17448421 | snp | C/T | 0.180383 | 0.240111 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360075 | TATTTGCTTAACCAA[C/T]GTCTTATGAAGTCCT | 23072 |
rs17545513 | snp | G/T | 0.493837 | 0.055168 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359722 | TCAAATGCATGCTAA[G/T]AAAATTGTAGACATT | 23072 |
rs17641812 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138774 | CATAAAACTGTTTTA[A/G]GATGAAAATAGAGCT | 23072 |
rs17641969 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | HECW1 | GRCh38.p7 | 7:43171622 | GCAGTACAATGAAAG[A/G]AAAAAAGGGGCGTTT | 23072 |
rs17642265 | snp | C/G | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43194561 | CCGCAAAACCTTGCT[C/G]AAATCAGAGACAAGG | 23072 |
rs17642283 | snp | A/G | 0.175254 | 0.238565 | intron-variant | HECW1 | GRCh38.p7 | 7:43197984 | CACATCTTTCCTGCC[A/G]TTGCCCCTAGGTCAT | 23072 |
rs17642825 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300061 | AGGCTTTGTCTTTGC[C/T]TCGTTGTGATTTCTT | 23072 |
rs17653768 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | HECW1 | GRCh38.p7 | 7:43321901 | AACTTATGGTATCCC[C/T]GCTCCCGGCAATGAC | 23072 |
rs17653815 | snp | C/T | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43329417 | GCTGATATTAGAGGC[C/T]TGAGACCACCAAGAA | 23072 |
rs17653845 | snp | A/G | 0.185155 | 0.241444 | intron-variant | HECW1 | GRCh38.p7 | 7:43332638 | GCAGATGGGAGCAAA[A/G]GCGGCTGCGGTCACT | 23072 |
rs17708918 | snp | A/G | 0.493583 | 0.0562802 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111410 | AGCTAAGGTTTGAAA[A/G]TGGTCTGCTTTGAGC | 23072 |
rs17708960 | snp | A/G | 0.17332 | 0.23795 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132356 | TTTGTCTTCACACTT[A/G]CTAATAGGGACAAAT | 23072 |
rs17709008 | snp | C/G | 0.234109 | 0.249494 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136170 | GTCTCTATGTGGGTT[C/G]TGCCTGAATCAGAGG | 23072 |
rs17709491 | snp | C/T | 0.40386 | 0.197046 | intron-variant | HECW1 | GRCh38.p7 | 7:43195503 | CCTGCTTGGTAGCCA[C/T]GCCTCTTATGTTACT | 23072 |
rs17709833 | snp | C/G | 0.0821764 | 0.185298 | intron-variant | HECW1 | GRCh38.p7 | 7:43267973 | ATACTGATAAACTTT[C/G]AAGCAGTACAAAATT | 23072 |
rs17710006 | snp | C/T | 0.100231 | 0.200173 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295887 | CATCTATGACATTGA[C/T]GTATTGTTTTTAATC | 23072 |
rs17710195 | snp | A/G | 0.188946 | 0.24243 | intron-variant | HECW1 | GRCh38.p7 | 7:43332735 | TGTTGTTTGGGGTAA[A/G]GCTACTGTCCTGAGT | 23072 |
rs17722661 | snp | A/G | 0.115788 | 0.21092 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134447 | AAATATGAATGGAAT[A/G]AACTTCCCACCTATA | 23072 |
rs17722673 | snp | A/C | 0.105214 | 0.203807 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138733 | TCAAGCAACAGTTTT[A/C]GGACGGAGTATTCCA | 23072 |
rs17723081 | snp | C/T | 0.215144 | 0.247558 | intron-variant | HECW1 | GRCh38.p7 | 7:43201712 | CTAGGGAATCTTGGT[C/T]AGAGAATTTGTCTGC | 23072 |
rs17723330 | snp | A/G | 0.274929 | 0.248754 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247294 | GGCATGTGCTAGATG[A/G]CAGGACATGGAAGAA | 23072 |
rs17723390 | snp | A/G | 0.105569 | 0.204058 | intron-variant | HECW1 | GRCh38.p7 | 7:43254119 | TTCCAGGCAAATCTT[A/G]ATTGACTGGTAATGA | 23072 |
rs17723413 | snp | A/G | 0.107341 | 0.205301 | intron-variant | HECW1 | GRCh38.p7 | 7:43261288 | TTTTTCCCCTTAAAC[A/G]GGAGCCTTATGTCTA | 23072 |
rs17723745 | snp | C/T | 0.498182 | 0.0300969 | intron-variant | HECW1 | GRCh38.p7 | 7:43332253 | CAAAGCCACTCTACA[C/T]ACAAAATGAATCTCT | 23072 |
rs17723805 | snp | C/T | 0.238171 | 0.24972 | intron-variant | HECW1 | GRCh38.p7 | 7:43337709 | CCTCTCCAACTCAGC[C/T]GAATAGCCAAGATCA | 23072 |
rs17795651 | snp | A/G | 0.115088 | 0.210473 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134815 | TTGACATATTATTCT[A/G]CCTTTGGTGATCATG | 23072 |
rs17795675 | snp | G/T | 0.487621 | 0.0776941 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139921 | AGCTTCAGTTTTCTG[G/T]TCTGTGAAATGGACT | 23072 |
rs17795844 | snp | C/T | 0.204189 | 0.245767 | intron-variant | HECW1 | GRCh38.p7 | 7:43179298 | CTGAAGTCTACAGCA[C/T]TGAGAGCAAAGGAGA | 23072 |
rs17796282 | snp | A/G | 0.107341 | 0.205301 | intron-variant | HECW1 | GRCh38.p7 | 7:43246909 | ACCCAGTGTTGGGTG[A/G]GAATGGCTAGACCCC | 23072 |
rs17796324 | snp | A/G | 0.106633 | 0.204807 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247309 | GCAGGACATGGAAGA[A/G]TAGGGCACTAAAATT | 23072 |
rs17796449 | snp | C/T | 0.364609 | 0.222182 | intron-variant | HECW1 | GRCh38.p7 | 7:43267819 | AATATATTTGAAAGA[C/T]TTGATGAGTTAATTT | 23072 |
rs17796504 | snp | A/G | 0.345925 | 0.230864 | intron-variant | HECW1 | GRCh38.p7 | 7:43274923 | TTAAAAAAATTAAAA[A/G]CTATACAACTCAATG | 23072 |
rs17796805 | snp | C/T | 0.148661 | 0.22854 | intron-variant | HECW1 | GRCh38.p7 | 7:43338094 | CCACTTAGATTGAAA[C/T]ACAGAGACCTACTCC | 23072 |
rs17800970 | snp | A/G | 0.19459 | 0.243782 | intron-variant | HECW1 | GRCh38.p7 | 7:43397280 | ACAGATAACTGAGCC[A/G]CTCAAAAATGCTCAT | 23072 |
rs17801421 | snp | A/G | 0.221737 | 0.248397 | intron-variant | HECW1 | GRCh38.p7 | 7:43434488 | GTTTATCTCACTCCA[A/G]AGGTTCTTTAGAGGC | 23072 |
rs17801445 | snp | A/G | 0.197393 | 0.244402 | intron-variant | HECW1 | GRCh38.p7 | 7:43435116 | ATTTCCCATCTTATT[A/G]GCATTTAGTGTTACA | 23072 |
rs17802356 | snp | C/T | 0.284995 | 0.247539 | intron-variant | HECW1 | GRCh38.p7 | 7:43498213 | GAAAATCGGGCTTAG[C/T]ATTCAGACACCTGGA | 23072 |
rs17803256 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HECW1 | GRCh38.p7 | 7:43530813 | ACCTCCAAATTGTTC[A/G]GCATGATGCCCTTGA | 23072 |
rs17803315 | snp | A/G | 0.188316 | 0.242271 | intron-variant | HECW1 | GRCh38.p7 | 7:43543094 | TAACATCAAATCTTC[A/G]GATCAAATGGGTTAC | 23072 |
rs17803369 | snp | A/G | 0.188 | 0.24219 | intron-variant | HECW1 | GRCh38.p7 | 7:43545300 | TCTATTCAAGAAAAC[A/G]AAGTCAACTACAAAT | 23072 |
rs17803447 | snp | A/G | 0.187685 | 0.242109 | intron-variant | HECW1 | GRCh38.p7 | 7:43551261 | CTTGGCACAAGATGC[A/G]AAGTCAGAATGCAGA | 23072 |
rs17803739 | snp | A/G | 0.315758 | 0.241197 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43564000 | GACTTTTATTGTCTA[A/G]AAAGAATATTTACTG | 23072 |
rs17885498 | snp | A/G | 0.284471 | 0.247612 | intron-variant | HECW1 | GRCh38.p7 | 7:43407918 | TGATCAAGTCCATCC[A/G]GACAGTACTAACACA | 23072 |
rs28373054 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43493456 | CAGAAAGGAAACAAA[A/G]TAGCTTCCATTAAAA | 23072 |
rs28376813 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336130 | TTTCTTTCTTTCTCT[C/T]TCTCTCTCTCTCTTT | 23072 |
rs28392184 | snp | A/G | 0.477175 | 0.104362 | intron-variant | HECW1 | GRCh38.p7 | 7:43308041 | ATTATATATTATATT[A/G]TATTATATATAATAC | 23072 |
rs28404008 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43179059 | CCTTCACAAGTAACA[A/C]CGAGGAAAAAGAAAG | 23072 |
rs28414569 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480694 | ATACGCATATATATA[C/T]ATACACACACACACA | 23072 |
rs28415181 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43552594 | TCCCCCAACCCCTGG[C/G]AACCATCAATCTGCC | 23072 |
rs28417784 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43315465 | CGTCCCATTATTATT[A/G]TTATTATTATTATTA | 23072 |
rs28455160 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480696 | ACGCATATATATATA[C/T]ACACACACACACACA | 23072 |
rs28464620 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480666 | GTGTGTGTATATATA[C/T]ACACACACATATATA | 23072 |
rs28478631 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141416 | CTTTGAAGCTAGTGG[C/T]TTTCTTAGAATGTGC | 23072 |
rs28479941 | snp | A/C | 0.168785 | 0.236441 | intron-variant | HECW1 | GRCh38.p7 | 7:43449446 | CCTGAATATATCTCT[A/C]CTTCTGTTTGCCAGT | 23072 |
rs28485630 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480672 | GTATATATATACACA[C/T]ACATATATACGCATA | 23072 |
rs28485734 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43480657 | TATGTGTGTGTGTGT[A/G]TATATATATACACAC | 23072 |
rs28491794 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43176980 | TATTTTTGAGGCTGG[A/G]GTTTGAAAATTTGCA | 23072 |
rs28530763 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488410 | GAAGGAAATGAAAGA[A/G]AGAGAGAGAGAGAAA | 23072 |
rs28533443 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43266396 | GCTGGAGTGCAGTGG[G/T]GCGATCTTGGCTCAC | 23072 |
rs28538839 | snp | C/T | 0.279991 | 0.248195 | intron-variant | HECW1 | GRCh38.p7 | 7:43251741 | CTGGTTATTTCCTCT[C/T]TTCTCCCTTATACAA | 23072 |
rs28540199 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43380231 | CTAATATTTTTAAAA[A/T]TTTTTAAATTTTTGT | 23072 |
rs28558854 | snp | C/T | 0.29046 | 0.246704 | intron-variant | HECW1 | GRCh38.p7 | 7:43379664 | AAGATGGTTCTTCCC[C/T]CAGGGCCCTTGCACT | 23072 |
rs28561841 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43501531 | TTACAGTTTGAAATG[A/G]TTGGGAAAAAAATGT | 23072 |
rs28568561 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43176981 | ATTTTTGAGGCTGGA[A/G]TTTGAAAATTTGCAT | 23072 |
rs28573786 | snp | C/T | 0.138886 | 0.22395 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126892 | CTCAATCAATAACTG[C/T]GGTGTGTGTTCTGAC | 23072 |
rs28578362 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519676 | GAATGGTTAAATGTA[C/T]TACAGCAGATCCACA | 23072 |
rs28582041 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225947 | GCTAACTTTTTTTTT[A/T]TTTTTAGTAGAGACG | 23072 |
rs28582832 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43174484 | ACCCTAATTACTTCT[C/G]TGCTTCCTTGATCTT | 23072 |
rs28584118 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43172159 | GGCACAATGGTGGGG[A/G]TGGGGGGATGTGTAA | 23072 |
rs28593587 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480655 | CATATGTGTGTGTGT[A/G]TGTATATATATACAC | 23072 |
rs28607540 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129635 | TTGAAAAACAAAAAC[A/G]AAACGGATAAAGGAC | 23072 |
rs28609971 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | HECW1 | GRCh38.p7 | 7:43215581 | TTGTATTATTAATAC[A/G]ATATCTATCCTAGTT | 23072 |
rs28622556 | snp | A/T | 0.492871 | 0.0592773 | intron-variant | HECW1 | GRCh38.p7 | 7:43284329 | AGTAACATATGCATT[A/T]TCTCACACACTTCTT | 23072 |
rs28624640 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141380 | CTTACCTCAGAGAAC[A/T]GCTGCACCTGGGGCT | 23072 |
rs28632040 | snp | C/G | 0.191461 | 0.24305 | intron-variant | HECW1 | GRCh38.p7 | 7:43318411 | CACTGTGAATAAAAA[C/G]ACAGGCAAATTTTGC | 23072 |
rs28645714 | snp | C/T | 0.14665 | 0.227637 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43270030 | ATGTCCACATTAGCA[C/T]TGTTGTAAGCCCTGT | 23072 |
rs28650865 | snp | A/G | 0.312348 | 0.242101 | intron-variant | HECW1 | GRCh38.p7 | 7:43363854 | ATTTGGCTATATGGT[A/G]ATGGAGCAGAACCAC | 23072 |
rs28657730 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480664 | GTGTGTGTGTATATA[C/T]ATACACACACATATA | 23072 |
rs28657828 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | HECW1 | GRCh38.p7 | 7:43368925 | TGACATTAGAAAAAA[A/T]TTATGGAAAGTGGAA | 23072 |
rs28680596 | snp | A/G | 0.084728 | 0.187577 | intron-variant | HECW1 | GRCh38.p7 | 7:43463238 | TTATATCAATTACCC[A/G]ACAAATAAAACTGAG | 23072 |
rs28687210 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509790 | GATTTGAAAATTACC[A/G]CTGTTCTGACTGCAG | 23072 |
rs28697022 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43174482 | TAACCCTAATTACTT[C/G]TCTGCTTCCTTGATC | 23072 |
rs28704873 | snp | A/G | 0.184521 | 0.241273 | intron-variant | HECW1 | GRCh38.p7 | 7:43273714 | AGGATATTTGACAAT[A/G]TAAAATGTTGAAGTT | 23072 |
rs28710446 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43552595 | CCCCCAACCCCTGGC[A/C]ACCATCAATCTGCCT | 23072 |
rs28718169 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336144 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 23072 |
rs28718777 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43404989 | GTCAAAAAAATCAAA[A/C]AAAAAAACAAAAGCA | 23072 |
rs28722033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43479004 | TTCCCCATTTAGATC[A/G]GTGGTCTCCAACCTT | 23072 |
rs28731163 | snp | A/C | 0.479583 | 0.0989539 | intron-variant | HECW1 | GRCh38.p7 | 7:43390549 | TCTTAAAAAAAAAAA[A/C]AAAAAAAAAACAGCA | 23072 |
rs28759310 | snp | C/T | 0.00835628 | 0.0640961 | intron-variant | HECW1 | GRCh38.p7 | 7:43493068 | TCAACCACAACTGTG[C/T]TTTTGTCTGTTTCAG | 23072 |
rs28776238 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416057 | ctccatccagctttg[C/T]tccgttgctggtgaa | 23072 |
rs28856380 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416058 | tccatccagctttgt[C/T]ccgttgctggtgaag | 23072 |
rs28860912 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336150 | TCTCTCTCTTTCTCT[C/T]TCTCTCTCTCTCTCT | 23072 |
rs33912005 | in-del | -/A/C/CA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43183971 | CAATTTAAAAAAAAA[-/A/C/CA]ATCAAGATGTGATTT | 23072 |
rs33937309 | in-del | -/AC/AT/TATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480685 | GCATATATATATATA[-/AC/AT/TATA]CACACACACACACAT | 23072 |
rs33941103 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43536796 | GCAAACTTCAAAAGA[-/C]GTCCCTGTAAACTCT | 23072 |
rs33990930 | in-del | -/TG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480612 | GTAGGTGAGTGAGTT[-/TG]TGTGTGTGTGCGTGT | 23072 |
rs33991644 | in-del | -/TG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480644 | GTGTGTGTGTACATA[-/TG]TGTGTGTGTGTGTAT | 23072 |
rs34030320 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43533984 | GAAGGTCACCCAAAG[-/A]CAGGAGACCCCTTGA | 23072 |
rs34030603 | multinucleotide-polymorphism | CC/GT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43259345 | TGAGCTGAGATCGCA[CC/GT]GCTGCGCTCCAGCCT | 23072 |
rs34043662 | snp | A/C | 0.161267 | 0.233723 | intron-variant | HECW1 | GRCh38.p7 | 7:43379921 | GATGTACCTGCCTGT[A/C]CTCTTCAGAGCTGTT | 23072 |
rs34047274 | snp | A/G | 0.272511 | 0.248984 | intron-variant | HECW1 | GRCh38.p7 | 7:43464258 | AAAAATTCACAGTAT[A/G]TTGCAAAGGAGCCAT | 23072 |
rs34048661 | in-del | -/G | 0.499767 | 0.0107802 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111410 | GCTAAGGTTTGAAAA[-/G]TGGTCTGCTTTGAGC | 23072 |
rs34056642 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506962 | TGATCCCAGCTACTC[-/G]GGGAGGCTGAAGTAG | 23072 |
rs34060757 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43206341 | TTAGGAAGACAGGGG[-/A]AGAGGAGAGGGAAAT | 23072 |
rs34068735 | in-del | -/A | 0.49263 | 0.0602539 | intron-variant | HECW1 | GRCh38.p7 | 7:43449791 | AGGAGGAACCATCTG[-/A]AAAAAGGGCCATCCT | 23072 |
rs34070957 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43243845 | TGCTTGGGATACACG[C/G]TAAGTTAACCTCGTT | 23072 |
rs34077474 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43391527 | GCTCTGTGCCACTCA[-/C]CCTGTGTTGCTTTCC | 23072 |
rs34077669 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43421640 | GCCACCACACAAAGC[-/G]GGGGATGTCCAAATG | 23072 |
rs34079442 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378809 | AGACTGTCTCAAAAA[A/C]CAAAAATAAAAACAA | 23072 |
rs34083261 | in-del | -/T | 0.484279 | 0.0872533 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134723 | TCAATATTTGGGGGA[-/T]TTTTTTTTCTTACTT | 23072 |
rs34085021 | snp | A/G | 0.242775 | 0.249896 | intron-variant | HECW1 | GRCh38.p7 | 7:43525859 | GGTACAGAGGAGAGG[A/G]GAGGCTTCCTACTTT | 23072 |
rs34085305 | snp | A/G | 0.343701 | 0.231776 | intron-variant | HECW1 | GRCh38.p7 | 7:43395938 | ATAGTGAGACTCTGA[A/G]CAAGAGATTATGGAT | 23072 |
rs34090257 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43259225 | AACCCTGTCTCTACT[-/A]AAAATACAAACATTA | 23072 |
rs34091784 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43295392 | AATTCCCAGCATGAA[-/T]TTTTCCCTGTGGCTT | 23072 |
rs34092356 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293572 | GTTCCCTGTCTCCAG[-/T]ACCCTATTCTGCTGC | 23072 |
rs34101126 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43442974 | AATGAATGAATGAAC[-/T]GTGAAACATCTTTCT | 23072 |
rs34104909 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43408830 | GGTATAATGTAGGTT[-/A]AAAAGTACAGTTTTA | 23072 |
rs34105302 | in-del | -/T | 0.196771 | 0.244268 | intron-variant | HECW1 | GRCh38.p7 | 7:43329147 | CAGGAACTCGGCCAG[-/T]TGGGAAGGAAGGTCT | 23072 |
rs34111268 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226384 | ACCCTGCCTCCCCAG[-/A]TGGGGTGATGATGTT | 23072 |
rs34125032 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43167093 | TCACAAACTTTATGG[-/C]CTAAAGCAACAGGAA | 23072 |
rs34128307 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43541126 | TAACAATGTAAATTT[-/C]CCACTTACCGATTTC | 23072 |
rs34130498 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43294738 | GGTCAGTCTGACTTC[-/A]AAAGCTTTTGTCCCC | 23072 |
rs34131950 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43341653 | ACAAACATCTACTGT[-/G]TTATTAAACATTTAT | 23072 |
rs34140960 | snp | A/G | 0.2768 | 0.248559 | intron-variant | HECW1 | GRCh38.p7 | 7:43363738 | CCCCCTTTGTTTGAT[A/G]GCGTGGCACACTTTT | 23072 |
rs34157616 | snp | C/T | 0.249886 | 0.25 | intron-variant | HECW1 | GRCh38.p7 | 7:43531529 | CAACAACCCAAACCT[C/T]CATGTCATGCCCTCC | 23072 |
rs34182731 | in-del | -/A | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516976 | AAATGGTACACCTGT[-/A]TAGGGCAGCTCCGTT | 23072 |
rs34186765 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43497355 | AAGTTGGAGAGGGAG[-/C]GCCCTATCACCAACC | 23072 |
rs34200636 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356949 | GAATAGACATTTCTT[-/A]AAAAGAAGACAGACA | 23072 |
rs34204818 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43397824 | TATGTGCAGGTCACA[-/G]GGGCATATGATGGCT | 23072 |
rs34206401 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43294316 | GACCTGACCACAACA[-/G]GGGAAGATCTCCAAG | 23072 |
rs34215532 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481970 | ACACAGCGAGACTCC[A/C]TCTCAAAAAAAAAAA | 23072 |
rs34224020 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422402 | AGTCTCGCTCTGTCA[-/C]CCCAGGCTGGAGTGC | 23072 |
rs34229964 | in-del | -/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43187340 | CCTTTCAAGTGGAGG[-/G]AAATTGGGCTCCACC | 23072 |
rs34238162 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43381490 | CCATGCATGGCTAAT[-/T]TTTTTTTTTTTTTTT | 23072 |
rs34255651 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546219 | CCTTTACCCCCAACC[-/T]TTTTTTTTTTTTTTT | 23072 |
rs34257122 | snp | A/G | 0.245061 | 0.249951 | intron-variant | HECW1 | GRCh38.p7 | 7:43239549 | TTTGGGGTCACTGAA[A/G]TAGGAATTGTATGTC | 23072 |
rs34259169 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529550 | CCATTTGACTGTCCC[-/A]AAAGCCTCCATCAAC | 23072 |
rs34260820 | snp | A/G | 0.257454 | 0.249889 | intron-variant | HECW1 | GRCh38.p7 | 7:43464391 | ATTTTTTCCCACTAC[A/G]GTAGGCATTCACCTT | 23072 |
rs34297527 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43427710 | CACTTGTGTTCTCAT[-/A]CTAGGGCCTTGTCTG | 23072 |
rs34301727 | in-del | -/ATC | 0.155325 | 0.23138 | intron-variant | HECW1 | GRCh38.p7 | 7:43203229 | TGCTATATTATCTTT[-/ATC]ATCATCAGTTGTGAT | 23072 |
rs34302457 | in-del | -/T | 0.467234 | 0.12373 | intron-variant | HECW1 | GRCh38.p7 | 7:43173847 | TGTTGTTTTAAATGA[-/T]TTTTTTTTTTTTTGG | 23072 |
rs34306090 | in-del | -/G | 0.471292 | 0.116318 | intron-variant | HECW1 | GRCh38.p7 | 7:43209184 | GGCATCAGACCCACT[-/G]AGCCCCTCACAATCT | 23072 |
rs34322130 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43553284 | CCCATCAATACAGTA[-/G]GAGAGTGAGCTGGGG | 23072 |
rs34323991 | snp | C/T | 0.417521 | 0.185571 | intron-variant | HECW1 | GRCh38.p7 | 7:43431089 | CCCCATTTTTATTTT[C/T]CTTTAACAATGTCTT | 23072 |
rs34336718 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | HECW1 | GRCh38.p7 | 7:43274009 | GGTCGCACCACCACA[C/T]GCAGTTAATTTTTGT | 23072 |
rs34340104 | snp | A/T | 0.0955749 | 0.196603 | intron-variant | HECW1 | GRCh38.p7 | 7:43345224 | ACATGTATGTAACAT[A/T]CAACCCAAGTTAACA | 23072 |
rs34347463 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289635 | CTGGCCCATAGGTGG[-/T]TCTTATTAACAGAAG | 23072 |
rs34351679 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354187 | AACATATCCAATAAT[-/A]AAAAAAAAAAAAAGG | 23072 |
rs34361756 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355339 | TCTAGTAGGAAGCCC[-/A]AAAGATAAATTGATC | 23072 |
rs34363937 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43329061 | TACTTCTTTTTGTGC[-/T]TTTGTGTGAAATAGT | 23072 |
rs34367656 | in-del | -/T/TTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43313340 | ACAGCCTAAAGAGCA[-/T/TTT]TTTTTTTTTTTTTTT | 23072 |
rs34381405 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43266991 | ATGATCCTCTACACT[-/C]CCTAATAGTATAGAA | 23072 |
rs34384663 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43273487 | TAAAGAATATATTAA[-/C]ACAATAAGTATTACT | 23072 |
rs34394088 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43443053 | AAGAACTATAATTGT[-/C]ACAATGAATTTTTAT | 23072 |
rs34399842 | snp | A/G | 0.0919665 | 0.193715 | intron-variant | HECW1 | GRCh38.p7 | 7:43466594 | TAAAATGCAGAGGGG[A/G]CGGCCTGGCTCGGCA | 23072 |
rs34402149 | in-del | -/A | 0.471673 | 0.115589 | intron-variant | HECW1 | GRCh38.p7 | 7:43369729 | GAGGACTTCTTAAAC[-/A]AAAGGCTTTTCTCTT | 23072 |
rs34406348 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43228554 | GAAGAACACTTGCAT[-/G]GGATCACCAGCTGGG | 23072 |
rs34417565 | in-del | -/T | 0.339203 | 0.233544 | intron-variant | HECW1 | GRCh38.p7 | 7:43234510 | CTCCCACCTCAGGCC[-/T]TTTTTTTTTGCCTGG | 23072 |
rs34418072 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237579 | AGACAGTTATAGGAA[-/C]CTGCCTCGCTAGATT | 23072 |
rs34421255 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358584 | CAATTAAATGGCTTC[-/A]AAAAAATTTAAATAG | 23072 |
rs34436949 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556276 | CAAGCAAGGGCTGAG[-/T]AGCGGGGAATGGCAG | 23072 |
rs34441737 | in-del | -/C | 0.0748431 | 0.178382 | intron-variant | HECW1 | GRCh38.p7 | 7:43547402 | AAATACAAAAATTAA[-/C]CAGGTGTGGTGGCAC | 23072 |
rs34445096 | in-del | -/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159669 | AAGCATTTCCTATTT[-/C]CCTTGTATCTTTTTT | 23072 |
rs34461041 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43527384 | CTCCAGGGGAGACCC[-/T]TTTTTTTACCTCTTT | 23072 |
rs34461571 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43394876 | ATTCAGGGGACAGAG[-/T]TTTTAACGATAACTT | 23072 |
rs34461582 | snp | C/G | 0.207253 | 0.246318 | intron-variant | HECW1 | GRCh38.p7 | 7:43559707 | ACTGCCCCACACCAC[C/G]GGGCAATGCTTGGTT | 23072 |
rs34462261 | in-del | -/G | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511662 | GCCCTGATCAGCTTT[-/G]GGGACATCTTAACAA | 23072 |
rs34462638 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43548245 | TCTAACTTTTTTTTT[-/T]CATTTTAAAAAAGCT | 23072 |
rs34488898 | snp | C/T | 0.173965 | 0.238157 | intron-variant | HECW1 | GRCh38.p7 | 7:43349183 | GGGATTACAGGCATG[C/T]GCCACCACGCCCGGC | 23072 |
rs34492078 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43325816 | CTCGTTTCCTCGTGT[-/G]GAAACCTGGCTGGAT | 23072 |
rs34503055 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43485379 | GATCACAGGTTTGGC[-/T]TGGAAGTTTGTAAAA | 23072 |
rs34507829 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43495315 | CCGCTCCCTGTGTCC[-/A]TGTGTTCTCGTTGTT | 23072 |
rs34508741 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426449 | TCTCTTGATTTCACA[-/G]GGAGGGATCATATGG | 23072 |
rs34511113 | in-del | -/TT/TTT | 0.492582 | 0.0604491 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135979 | CTTTTTTTTTTTTTT[-/TT/TTT]ACTATTTGCTGATAG | 23072 |
rs34513677 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43547797 | TTTTCTCTGCTTCTT[-/G]GGGAGTATTTCCAGC | 23072 |
rs34526729 | snp | A/G | 0.257732 | 0.24988 | intron-variant | HECW1 | GRCh38.p7 | 7:43460116 | GGCCTGCTAAATACT[A/G]AGATTGCCTTATAGT | 23072 |
rs34529429 | in-del | -/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127270 | GCTCATGCCTGTAAT[-/C]CCCAGCACTTTGGGA | 23072 |
rs34546630 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43290307 | TACCACAGTCAGTTT[-/G]GGAAAGTAAGCCACA | 23072 |
rs34563804 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43447169 | AAGCTTTTTTTTTTT[-/T]GTATTAAAAAGTGTA | 23072 |
rs34571187 | in-del | -/A | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119882 | CGTCTAAGCGCTAGT[-/A]AAGCTTTCCTAACTG | 23072 |
rs34578029 | snp | A/C | 0.46845 | 0.121572 | intron-variant | HECW1 | GRCh38.p7 | 7:43451864 | TCCAGAATGCAAGGA[A/C]CCAGTGTTTCTTTAC | 23072 |
rs34583245 | snp | C/G | 0.191775 | 0.243125 | intron-variant | HECW1 | GRCh38.p7 | 7:43338999 | TCTCTTTAGCACTTA[C/G]GAATGTCATTTATCT | 23072 |
rs34583353 | snp | G/T | 0.338069 | 0.233974 | intron-variant | HECW1 | GRCh38.p7 | 7:43531384 | GTCTATCTCCCTTCC[G/T]AGCTTGTAAACTCAA | 23072 |
rs34597695 | snp | C/T | 0.223522 | 0.248594 | intron-variant | HECW1 | GRCh38.p7 | 7:43386090 | CCTTCATGCCGCCCA[C/T]ATTCCTTACCACGTG | 23072 |
rs34610745 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | HECW1 | GRCh38.p7 | 7:43294976 | ACATTGATTCAGTCC[A/G]GAAAGCAGGACAACG | 23072 |
rs34627332 | in-del | -/C | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296454 | GTGGTGACAGTGAGG[-/C]CCCCTGGTTCATGAC | 23072 |
rs34646506 | in-del | -/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135576 | CATGGCTTGTTTGGT[-/G]CAATGTCTGAACAAA | 23072 |
rs34650656 | snp | A/C | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519234 | GCAATCACATGCAGT[A/C]TGACTCTAGAGTGCA | 23072 |
rs34664394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43459974 | GCATTTAATATTGCC[A/G]CATAGTCTTCAGGTT | 23072 |
rs34686016 | in-del | -/T/TT/TTT | 0.448323 | 0.15221 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115299 | CAACTCAAACAGGTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 23072 |
rs34688132 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356609 | TTTCTATCAACACAT[-/G]GGAACATTCTTCAGA | 23072 |
rs34698569 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327246 | AGGTTTTCTGTTAGG[-/A]AAAAGTATGACTCCA | 23072 |
rs34701274 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43240032 | GTTTCTATAATTAGG[-/A]AAAAAAGTTTTTTTT | 23072 |
rs34703311 | snp | A/G | 0.321292 | 0.23962 | intron-variant | HECW1 | GRCh38.p7 | 7:43538154 | GACCTAGGTCAGAGG[A/G]AGTCAAGTTGGTCTC | 23072 |
rs34703827 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43427990 | CAAGGTCCGTTGTTT[-/G]GGTAATCTAATCATG | 23072 |
rs34705314 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43501656 | GCAACATAGCGAGCT[-/C]CCCTTCTCTACAAAA | 23072 |
rs34706840 | snp | A/C | 0.17332 | 0.23795 | intron-variant | HECW1 | GRCh38.p7 | 7:43189600 | AAAACACATTAAAAA[A/C]AAGAAAGAGAGAAAA | 23072 |
rs34707380 | in-del | -/T | 0.436265 | 0.166749 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117528 | CATTGCTTTTCCAAG[-/T]TTAAGACACAATGAG | 23072 |
rs34707960 | in-del | -/A | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124701 | GGATAGGGGACTGGG[-/A]AGTAGCCAGGAGCTT | 23072 |
rs34709911 | snp | C/T | 0.163236 | 0.234461 | intron-variant | HECW1 | GRCh38.p7 | 7:43382425 | AAAGTTAATTAGTAC[C/T]GTTTTGTGAGCTTTT | 23072 |
rs34710878 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43433350 | ACCCAGTTGCACAGT[-/G]GGAGTCACCTGATAA | 23072 |
rs34712026 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43530344 | CTGACATGCCATTGT[-/G]CACCTAGTTTTTATT | 23072 |
rs34718117 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43366807 | CAAAAAGGAGTATCC[-/A]AAAACTAATGGAGAA | 23072 |
rs34718292 | snp | C/T | 0.257176 | 0.249897 | intron-variant | HECW1 | GRCh38.p7 | 7:43423442 | CTTGTTCTACAGTGA[C/T]GCCTGAGGCTCATTC | 23072 |
rs34722832 | snp | A/G | 0.279991 | 0.248195 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521324 | ACCCCCAGCTGTCAC[A/G]ACCAAAAATGTTTCC | 23072 |
rs34729904 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43207885 | CATTACTTTTGAGAT[-/A]ATCTTTCTTCTCTTG | 23072 |
rs34730445 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43405714 | TACACAAACACTTTA[A/G]GCACAGTGAGCCACT | 23072 |
rs34735793 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356709 | TCTCTGACCACAAAA[-/G]GGAATAAAACAAAAT | 23072 |
rs34736444 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43554460 | CCTCTCTAAAGGCCA[C/T]CACAAGAGAAATCAG | 23072 |
rs34737241 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347883 | CCATTTGATCATGGT[-/G]GGATTATCTTTTTGA | 23072 |
rs34740211 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43346465 | ATTCTCCTGACTGTT[-/C]CCTTGTGCCATGCAA | 23072 |
rs34744352 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43466658 | AGATCTAAAAGGGTA[-/G]GAATTTTAACATAAG | 23072 |
rs34748611 | in-del | -/A/AA/AAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293219 | GCGAGACTATGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 23072 |
rs34750405 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43526809 | GTTTGAGACTACCCT[-/G]GGGCAACATAGCAAG | 23072 |
rs34753661 | in-del | -/A | 0.179425 | 0.239831 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376866 | CAAGGACTCTGTCTC[-/A]AAAAAAAAAAGACAT | 23072 |
rs34756487 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43231968 | GGAGCTTGCAGTGAG[-/C]CTGAGATCCCACCAC | 23072 |
rs34761637 | snp | A/G | 0.271162 | 0.249103 | intron-variant | HECW1 | GRCh38.p7 | 7:43464451 | GAATTTGCCCAAGTG[A/G]GACTCAGACAAGGAT | 23072 |
rs34774635 | snp | A/T | 0.0752113 | 0.178743 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129118 | AAACATAGTTGATAA[A/T]GCAGCAGCAGGGTTT | 23072 |
rs34776149 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454713 | CTATGTACATATAAA[-/G]ACCATAAATATGCCA | 23072 |
rs34787294 | snp | C/G | 0.172351 | 0.237636 | intron-variant | HECW1 | GRCh38.p7 | 7:43399715 | TTATAAGGTGATCAG[C/G]GTTGGTTCATCTCCT | 23072 |
rs34791514 | in-del | -/A | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43232042 | AAAAAAAAAAAAAAA[-/A]GGAACCTCTTGGAGG | 23072 |
rs34806946 | in-del | -/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156422 | TATCTTAGTACCTCT[-/G]GGAAAGATCAAACTA | 23072 |
rs34816689 | in-del | -/AT/TA | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43405254 | GTTTTATATATATAT[-/AT/TA]GTCTTTCACACTCTA | 23072 |
rs34828609 | snp | A/G | 0.262985 | 0.249663 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522184 | TTTTGTTATAGCCAC[A/G]GGAATGAACTAAGAC | 23072 |
rs34831644 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43396330 | GAAGAGCTCCTTAAT[-/G]GCCTTGTTCAGGCTC | 23072 |
rs34836537 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43436248 | TCAGGTGTTTCACAG[-/C]CCCTTGATTAAGGGG | 23072 |
rs34836640 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210535 | TGTTGGGCCACTTCC[-/A]AAGATGGCTGCAAGC | 23072 |
rs34836709 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43262836 | ACCTTCTCCCTACTT[-/C]CCCAGTCCCCAGGCC | 23072 |
rs34840204 | in-del | -/AG | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43185414 | AGTCGGAACTGTCTC[-/AG]AATTATAGGTGACAG | 23072 |
rs34846023 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43366822 | AAAACTAATGGAGAA[-/G]GGAGAGTTTGTTCTC | 23072 |
rs34856587 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43279279 | CAAAGCAAAATGCTT[-/G]CTCTGTGTCCTTTTT | 23072 |
rs34862924 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43540245 | TTGGAAATTCCACCA[-/G]GGGAGGATCTGAGAA | 23072 |
rs34877754 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | HECW1 | GRCh38.p7 | 7:43351376 | CTTTCCAGAGAGTTT[C/T]GGCTGTAGTAGTATG | 23072 |
rs34879817 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43362132 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 23072 |
rs34896588 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43528113 | TTGACCATGAAAGGC[-/G]TGCTTGCCTGGATAA | 23072 |
rs34901433 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125388 | TTGCTCTGAGTCCAG[-/T]AATGAAAAGTAGCGG | 23072 |
rs34906627 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43324622 | TTACAGAAGCTTCTA[-/C]TTATGAACTAAAAAT | 23072 |
rs34933689 | snp | A/G | 0.377977 | 0.21476 | intron-variant | HECW1 | GRCh38.p7 | 7:43328229 | CTACTTGGGAAGCTG[A/G]GATGGGAGAATCACT | 23072 |
rs34938337 | snp | A/C | 0.481319 | 0.0948228 | intron-variant | HECW1 | GRCh38.p7 | 7:43408374 | GTTAGGAGGGTCCTC[A/C]AAGTTCTCTCCTAAA | 23072 |
rs34954809 | snp | C/T | 0.485255 | 0.0845871 | intron-variant | HECW1 | GRCh38.p7 | 7:43383244 | GCTACAATAAACATA[C/T]GTGTGCATGTGTCTT | 23072 |
rs34962349 | in-del | -/T/TT | 0.104859 | 0.203554 | intron-variant | HECW1 | GRCh38.p7 | 7:43500103 | GAGCCAAGAACAGTC[-/T/TT]TTTTTTTTTTTTTTT | 23072 |
rs34975931 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43479292 | ATAAGGAGTGTGCAA[-/C]CCCAGATCCCACACA | 23072 |
rs34977691 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260547 | TCATGAAGCAGCAAA[-/T]TTTGTGTTTGAAAAA | 23072 |
rs34990901 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | HECW1 | GRCh38.p7 | 7:43362563 | TCTTCCAGGCCCGTT[C/T]GTTTGGGCATCCCTC | 23072 |
rs34994648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43436056 | ATAGTCCCAGCTACT[C/T]GGGAGGTTGAGGCAG | 23072 |
rs34996078 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43432381 | CTGACCTCGTGATCC[-/G]GCCCGCCTCGGCCTC | 23072 |
rs35011075 | in-del | -/ATTA | 0.143622 | 0.226238 | intron-variant | HECW1 | GRCh38.p7 | 7:43528051 | AAGCTATTTTGGTCC[-/ATTA]ATTAACTACTTTGAT | 23072 |
rs35020395 | in-del | -/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155602 | TGTATAGTGAACACA[-/G]GGGAGGTTGATTTAA | 23072 |
rs35020884 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43176952 | GCCTCTTCCTGAGAT[-/C]CCCTTAGATTACTAT | 23072 |
rs35024091 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43325820 | TTCCTCGTGTGGAAA[-/T]CCTGGCTGGATGCAC | 23072 |
rs35040691 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | HECW1 | GRCh38.p7 | 7:43378837 | CAAAAGAAGGAGGCA[A/G]TGTCAGGCAAGGGCA | 23072 |
rs35068892 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43311741 | GCCCTGACCCTGCTC[-/T]ACTGTCTCTTTGCTC | 23072 |
rs35069455 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43397619 | TCACCAAGTACATTT[-/C]CAAGGGTGGGGAGAA | 23072 |
rs35074214 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189384 | GGGACATTGCTGGTC[-/C]ACAGATTACACAGTG | 23072 |
rs35085274 | in-del | -/TT | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126068 | TGAGTTTGTTCTCAC[-/TT]TTTTTTTTTTTTTTT | 23072 |
rs35096209 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43432145 | TGTTTATTTTATTTC[-/T]TTTTTTTTTTTTGAG | 23072 |
rs35098929 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129290 | CCACGGTCACCCAAC[C/T]TTCAGTAACCACCAC | 23072 |
rs35107410 | in-del | -/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120250 | ATACTGTTCCCTTGA[-/C]CTGGAGGGACGGTCC | 23072 |
rs35113641 | snp | C/G | 0.173965 | 0.238157 | intron-variant | HECW1 | GRCh38.p7 | 7:43346470 | TCCTGACTGTTCCTT[C/G]TGCCATGCAAAAGCT | 23072 |
rs35132099 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361975 | GGTGAAACGCTGTCT[C/T]TACTAAAAATACAAA | 23072 |
rs35140119 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43401108 | GTCCCTTTTACCATG[-/T]TAAGGTAACATATTC | 23072 |
rs35148844 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43218827 | GTCTCACGTGATTTA[-/G]GATAAAATGACACGG | 23072 |
rs35150373 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43203199 | TACTTATTATATTTC[-/A]AAATAGTTTTATTTT | 23072 |
rs35153636 | in-del | -/T | 0.425894 | 0.177655 | intron-variant | HECW1 | GRCh38.p7 | 7:43411052 | TATTTTTTTTTTTTT[-/T]AGCTCCTTAGGGTAA | 23072 |
rs35162690 | in-del | -/C | 0.494057 | 0.0541878 | intron-variant | HECW1 | GRCh38.p7 | 7:43178314 | CTGGCCAGCAGGGTT[-/C]CTATCTAACTATCCC | 23072 |
rs35165812 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43461692 | CCACCACAGATGTAC[-/G]GGGGTGGTGAATTAC | 23072 |
rs35167843 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43540984 | CCTAACAAGCACACA[-/G]GGGATTGTTCATGGT | 23072 |
rs35185832 | in-del | -/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360108 | TTAACAGGGGGTACA[-/G]GGGACTTATTCATTG | 23072 |
rs35196404 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43333175 | TGGTATGATAGGCAA[-/G]GGAAATGTGGGGGGC | 23072 |
rs35196555 | snp | A/T | 0.0337553 | 0.125452 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563874 | ACACCATCTAAAAAA[A/T]AAATAAATAAAAATA | 23072 |
rs35199868 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213463 | TGGTGATCATAAGAA[-/T]TTTTTTTTTTTTTTT | 23072 |
rs35203228 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43541269 | TGAGACTGTAAGTGC[-/T]TTTGCAGACCATGCT | 23072 |
rs35212650 | snp | C/T | 0.498392 | 0.028309 | intron-variant | HECW1 | GRCh38.p7 | 7:43446796 | GAAAGGTAAAACAGA[C/T]AGCATGGAAAGGTAC | 23072 |
rs35215427 | snp | C/T | 0.499598 | 0.0141716 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159766 | GCTCACTGCAAGCTC[C/T]GCTCCCAGGTTCATG | 23072 |
rs35220907 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43244066 | CTCAAGTGTGGCTGG[-/C]ACATTTGAGATCCAT | 23072 |
rs35227272 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43191910 | AATTGGTGCTCCTTT[-/A]AAAAGTGGCACATTA | 23072 |
rs35257642 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43249918 | ACGGCTTTGCAAATG[-/T]TTCTGCGGCAGTCTC | 23072 |
rs35274705 | in-del | -/A | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114099 | TTTGTGCTTACTTCT[-/A]CTTGGAATCTGCAGT | 23072 |
rs35278384 | snp | A/G | 0.275464 | 0.2487 | intron-variant | HECW1 | GRCh38.p7 | 7:43531681 | ATGAAGATTGCCAAA[A/G]CCATCTGGTGACCTC | 23072 |
rs35280012 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43320914 | AAGTGGTGAGGTCTA[-/G]GGGCAGTTGGATAAA | 23072 |
rs35304045 | snp | A/G | 0.404035 | 0.196909 | intron-variant | HECW1 | GRCh38.p7 | 7:43526891 | GTCCCTGCTACTCGG[A/G]AGACTAAGGCGAGAG | 23072 |
rs35304791 | in-del | -/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141894 | CTGGCGACTTGGAGT[-/G]CTATGAGCCGGACAC | 23072 |
rs35312789 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43193961 | CAAAAAAGATATTTT[-/G]GAGTAAAATGCTTTG | 23072 |
rs35356971 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517148 | AGGATTTTCAGGGCC[-/A]GATTTCAGATTTGAT | 23072 |
rs35364644 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556221 | AGGATTGGGAGGCAA[-/G]GGAATAGGGAGAAGG | 23072 |
rs35378292 | in-del | -/TTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179557 | TATTTGCTAAGTTTG[-/TTGT]TTGTTGTTGTTGTTG | 23072 |
rs35389558 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43314686 | AGCTACACATATATA[A/C]CTGTGAAGTTATGTA | 23072 |
rs35390708 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210034 | AGTTGAGAGAAACTT[-/A]AAAATCTACTGCTCT | 23072 |
rs35396094 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308547 | ATTTTAAGTTCATCT[-/C]CCTTCCTACATAACT | 23072 |
rs35403812 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43492898 | TTAGTTTGATCCCTT[-/A]AAAAATTATAATGTT | 23072 |
rs35406932 | snp | A/G | 0.494896 | 0.0502606 | intron-variant | HECW1 | GRCh38.p7 | 7:43465577 | CTTCTGACATGTTCT[A/G]TTGGTTGAAACAAGG | 23072 |
rs35408234 | in-del | -/A | 0.273856 | 0.248859 | intron-variant | HECW1 | GRCh38.p7 | 7:43547550 | GACTCTGGCTCAAAG[-/A]AAAAAAAAAAAGCTG | 23072 |
rs35410708 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237799 | TGGTGACAGATTTTG[-/A]AAATAGAGGCAGAAA | 23072 |
rs35412896 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43221698 | AGCTGGGACTACAGG[G/T]GCCCACCACCACGCC | 23072 |
rs35414360 | in-del | -/AA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134393 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 23072 |
rs35421676 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198626 | CACTCATTCACACAC[-/G]CATAGTCACACACCC | 23072 |
rs35422462 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43305400 | AATCTCAATTACTGC[A/C]ATTCTGTCCATCTGT | 23072 |
rs35431658 | in-del | -/GTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179556 | ATATTTGCTAAGTTT[-/GTT]GTTGTTGTTGTTGTT | 23072 |
rs35436159 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43165488 | TCATTAATAACAATT[-/C]CAATCAATTATCCGT | 23072 |
rs35437938 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268941 | ACCAACCCTTGCTGA[-/T]TTTTTCTATTTTCTA | 23072 |
rs35465449 | in-del | -/A | 0.499933 | 0.00579035 | intron-variant | HECW1 | GRCh38.p7 | 7:43342870 | CTCTACTAAAGATAC[-/A]AAAAAATCAGCTGGT | 23072 |
rs35466782 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43478011 | CAAAGGGTTTTGTTG[-/A]AAAAAAAGGTAATAA | 23072 |
rs35474408 | snp | A/G | 0.17332 | 0.23795 | intron-variant | HECW1 | GRCh38.p7 | 7:43345282 | AATTACTATTAGGCC[A/G]TATACATCAAAAGCT | 23072 |
rs35476922 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43357098 | CTGGTGAGAACACAG[-/T]AAAAAGGGGAGCCCT | 23072 |
rs35480568 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43475798 | AACTCCCAAGCTCAA[-/G]GAGATCCACCTACTT | 23072 |
rs35481808 | in-del | -/A | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43345852 | ATATACACACACATC[-/A]TATATATATATACAC | 23072 |
rs35490041 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43400243 | CTGCTTCAAAAGACT[-/A]AAAATAAAATAAAAA | 23072 |
rs35492135 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43458269 | AGGGTATCGTCAGGC[-/G]TGTATTCATAAGAGG | 23072 |
rs35492443 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43464205 | TGTATTTGTTGGTGT[-/C]TCTAAGGATTTTTTC | 23072 |
rs35493447 | snp | C/T | 0.324855 | 0.23853 | intron-variant | HECW1 | GRCh38.p7 | 7:43397241 | TTGTCTAAACAAAAC[C/T]TCACATGGGGCACAA | 23072 |
rs35514918 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43379594 | CCTGACACTGCCTCA[-/T]TCTTTCCACCTAATT | 23072 |
rs35517144 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358769 | GAAGTGTAAAGTGTT[A/G]TTTGGAAAGCAATTT | 23072 |
rs35521413 | in-del | -/T | 0.0592699 | 0.161623 | intron-variant | HECW1 | GRCh38.p7 | 7:43547581 | GTTTTCAATATGAGA[-/T]TAAAAAGATATTCCA | 23072 |
rs35532038 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481324 | GTTGAATATGCCTTT[-/A]AAAAGTTCAAGCTCT | 23072 |
rs35544162 | in-del | -/G | | | frameshift-variant | HECW1 | GRCh38.p7 | 7:43311896 | ACAACATGGACCTCA[-/G]GGGCGGCCCCCACGA | 23072 |
rs35551485 | snp | A/T | 0.286042 | 0.247388 | intron-variant | HECW1 | GRCh38.p7 | 7:43544634 | TACATTAACACCTAA[A/T]TAAAATTACTAATAT | 23072 |
rs35558159 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347435 | CTGGAGGAGTCCTTA[-/G]GGTTTTCAAGGTAAA | 23072 |
rs35565242 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43202631 | GCACCTGCCACCACG[-/C]CCCAGCTAATTTTTG | 23072 |
rs35572177 | snp | A/G | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358846 | TTTTTTTTTTTTGAG[A/G]CTGAGTCTTGCTCTG | 23072 |
rs35578773 | snp | A/C/G | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119105 | CACCCACCATGCAGC[A/C/G]TGAGACCAGAAGATC | 23072 |
rs35598355 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43175811 | AGCCTTCATGACGGC[-/T]TTTTGGTTGTTCTAG | 23072 |
rs35602944 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | HECW1 | GRCh38.p7 | 7:43360574 | CAGGTGATAGGCATC[C/T]ACCCACCTCACATCT | 23072 |
rs35603835 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43218399 | GACGTATCATGGATC[-/T]TGAACACAGCAGTGG | 23072 |
rs35618213 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43543790 | AAAACTCCATCTCAC[-/A]AAAAAAAAAAAAAAA | 23072 |
rs35619002 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166433 | TAAGCTAGATGCCTA[-/C]CCCAAGCTATAATAG | 23072 |
rs35620742 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43266626 | GCGTGAGCCACCGTG[-/C]CCCGGCCTCAGGAAA | 23072 |
rs35635411 | in-del | -/T | 0.29432 | 0.24604 | intron-variant | HECW1 | GRCh38.p7 | 7:43537549 | CATTACTAGAAGGTG[-/T]TTTTCTCATTCATGG | 23072 |
rs35638251 | in-del | -/G | 0.492337 | 0.0614248 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139813 | TCATCTTTGGAAAAA[-/G]GGGCAAATTTGGGGA | 23072 |
rs35642253 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | HECW1 | GRCh38.p7 | 7:43344901 | AATTCTTTGCTAGTA[A/G]TTTCAATCTTGTCTT | 23072 |
rs35643419 | snp | C/T | 0.306431 | 0.243548 | intron-variant | HECW1 | GRCh38.p7 | 7:43185420 | GAACTGTCTCAATTA[C/T]AGGTGACAGCCTGCT | 23072 |
rs35645175 | snp | A/G | 0.287867 | 0.247116 | intron-variant | HECW1 | GRCh38.p7 | 7:43450552 | CACTTTCTGATTCAG[A/G]AAATTCGGGTCATTA | 23072 |
rs35645190 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144456 | TTGAAAGCAGACACC[-/T]TACCTACCTATGGAA | 23072 |
rs35656366 | snp | C/T | 0.198944 | 0.244731 | intron-variant | HECW1 | GRCh38.p7 | 7:43340646 | TTTTTGAATTTAGAA[C/T]TGGCCCCCTGACACG | 23072 |
rs35661780 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43229755 | ATATTTATGTAATTT[-/C]CCGAGTGTCTCTCCA | 23072 |
rs35664967 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43192546 | AAAGAAAAAAGTGGT[-/A]ACACTATTGAAGATT | 23072 |
rs35692655 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43433300 | ACATTATTTGATATT[-/A]AAAATAGATTATTAC | 23072 |
rs35710120 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43276188 | ATAACAACTATGCCA[-/G]GGGACAGTTTATTTT | 23072 |
rs35717249 | snp | C/T | 0.138546 | 0.223781 | intron-variant | HECW1 | GRCh38.p7 | 7:43331290 | GGTTTCTAGCTTCAT[C/T]CATGTAAGATCGGGG | 23072 |
rs35723760 | snp | A/G | 0.19646 | 0.2442 | intron-variant | HECW1 | GRCh38.p7 | 7:43329208 | GGAAGGGGTGAGGCT[A/G]GGGTAGGTGAGACAG | 23072 |
rs35731936 | in-del | -/GAACCCCACC | 0.219349 | 0.248114 | intron-variant | HECW1 | GRCh38.p7 | 7:43327184 | CTACATGAGGAGACT[-/GAACCCCACC]TGTGCAACGTAAAGG | 23072 |
rs35735861 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214764 | GGGCACGGGCACTAG[-/C]CCCAGAAGGAGGAGG | 23072 |
rs35744264 | in-del | -/AAAG | 0.364817 | 0.222075 | intron-variant | HECW1 | GRCh38.p7 | 7:43268013 | TTATCACAGACAAAT[-/AAAG]ATAGAACACTTGCCA | 23072 |
rs35746924 | in-del | -/G | | | splice-acceptor-variant | HECW1 | GRCh38.p7 | 7:43311761 | CTCTTTGCTCCCACA[-/G]GAATCTGTACCAGAA | 23072 |
rs35748935 | snp | A/G | 0.173965 | 0.238157 | intron-variant, nc-transcript-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512101 | CCACCTTCTGAGGGA[A/G]TTCATCAGGAGATTC | 23072 |
rs35773028 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43430146 | CACAGACTGGAGTCA[-/T]TTTTTTCTCATACCT | 23072 |
rs35784045 | snp | A/G | 0.461592 | 0.133149 | intron-variant | HECW1 | GRCh38.p7 | 7:43259401 | CCAAAAAAAAAAACC[A/G]TTCAATATATAATTT | 23072 |
rs35789952 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133404 | CTTGGGCTTTATGCC[-/T]TTTTTCCGTATCAAT | 23072 |
rs35812491 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | HECW1 | GRCh38.p7 | 7:43470756 | TCACACACACACACA[C/T]AAATGGTCTCAGCAA | 23072 |
rs35821915 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43390403 | TAATTTGCCAGGCAT[-/G]GGTGGTGCACATCTG | 23072 |
rs35824970 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43290895 | TTTTCAGTCCAGGGA[-/G]GAATAGCAGGACGAG | 23072 |
rs35836167 | snp | A/G | 0.095934 | 0.196885 | intron-variant | HECW1 | GRCh38.p7 | 7:43337849 | TCACTTGCTGTGAAG[A/G]CTGCATTTGCAGTGT | 23072 |
rs35849120 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43278132 | CCTGAATGTTCCCCT[-/G]GAATATTCAGCTCCT | 23072 |
rs35849689 | in-del | -/G | | | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163427 | ACCCTTGTTCTGTCC[-/G]GGGGGGAGGTGCTGC | 23072 |
rs35851756 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343644 | TGTATATGTGCCACA[-/T]TTTTCTTAATCCACT | 23072 |
rs35853883 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43329031 | TTCTGGCATTACACT[-/G]GGGGAGACAAGCATG | 23072 |
rs35853922 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | HECW1 | GRCh38.p7 | 7:43311099 | TCTCATCAGGTACAA[C/T]GTTTTCTACAATAAC | 23072 |
rs35856637 | in-del | -/TATA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161814 | CCTAATTCCCATATA[-/TATA]CACTTCTCTGCAAAG | 23072 |
rs35862072 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454017 | TACATTCCAGGTATT[-/C]TAATGTATTGACAAA | 23072 |
rs35866398 | snp | C/T | 0.303938 | 0.244112 | intron-variant | HECW1 | GRCh38.p7 | 7:43216874 | TGCCCAGGCTGGCCT[C/T]GAACCCCTGGCCTCA | 23072 |
rs35892407 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43530116 | ACCATGCTTGGCTAA[-/T]TTTTTTTTTTTTTTT | 23072 |
rs35897956 | in-del | -/A | 0.420574 | 0.182769 | intron-variant | HECW1 | GRCh38.p7 | 7:43545836 | TGGAGGAGGTGGAAG[-/A]GGGGGCAGGAGAGGC | 23072 |
rs35902319 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43470806 | CACACATACACACAC[-/T]TCATAGTTACAGAAT | 23072 |
rs35917550 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43324267 | GTAGTATAATTTGTC[-/A]AAAAGTAAAAATTTA | 23072 |
rs35927018 | snp | G/T | | | synonymous-codon | HECW1 | GRCh38.p7 | 7:43550528 | CATCGAGCGCATGGT[G/T]AAGTGGCGGGTGGAG | 23072 |
rs35944261 | snp | C/T | 0.345704 | 0.230956 | intron-variant | HECW1 | GRCh38.p7 | 7:43435929 | CAGCACTTTGGGAGG[C/T]CGAGGCAGGCGGATC | 23072 |
rs35945340 | snp | C/T | 0.397813 | 0.201621 | intron-variant | HECW1 | GRCh38.p7 | 7:43335544 | CCACCAGCACCTTGA[C/T]ATTGAACTTTCCAGC | 23072 |
rs35947019 | in-del | -/C | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511648 | GATTTCAACAGGAAG[-/C]CCCTGATCAGCTTTG | 23072 |
rs35959896 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117381 | AACTTCCTATAACAT[-/C]CCCCCACATACATAA | 23072 |
rs35960515 | snp | A/G | 0.233235 | 0.249437 | intron-variant | HECW1 | GRCh38.p7 | 7:43535168 | GTTGGCAAATGGCCC[A/G]AAGAAGAGTCAAGTC | 23072 |
rs35966500 | snp | G/T | 0.0858192 | 0.188533 | intron-variant | HECW1 | GRCh38.p7 | 7:43349457 | TGTCAGTGAAGTATT[G/T]AAGTTCCCCCACTAC | 23072 |
rs35969094 | snp | A/G | 0.16911 | 0.236552 | intron-variant | HECW1 | GRCh38.p7 | 7:43497088 | GAATTCAGCAATAGT[A/G]GATAATATGCTGGTG | 23072 |
rs35969276 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43373316 | TAGATTCAAGTGATT[-/C]CTCCTACCTGAATTT | 23072 |
rs35992855 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192300 | TGACTCATTAACATT[-/A]AATTGGTTATACATT | 23072 |
rs35995427 | snp | C/T | 0.202343 | 0.245416 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143159 | TAGTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT | 23072 |
rs35996647 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43388840 | CCATGCAGCCCACTG[-/C]CCCAGCCTTACCTGT | 23072 |
rs36003280 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43542191 | TTAAACAATAACTTT[-/C]CCATTTCTCCCACCC | 23072 |
rs36007503 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | HECW1 | GRCh38.p7 | 7:43244538 | TTTACTGGGCACCAT[C/G]AATCATGGTTTGTGC | 23072 |
rs36014678 | snp | A/G | 0.2768 | 0.248559 | intron-variant | HECW1 | GRCh38.p7 | 7:43363715 | TTCATAGGAGCCACT[A/G]GGAGGAGCCCCCTTT | 23072 |
rs36026811 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43204908 | GAGAGCTATCTCACT[-/G]GAATGTTTGCATTTC | 23072 |
rs36028332 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43442988 | CGTGAAACATCTTTC[-/T]TACCTAGTAACTAGA | 23072 |
rs36029568 | in-del | -/TATTT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130866 | AAATGCTCAACCTGT[-/TATTT]ATTAATAACTGGGTA | 23072 |
rs36037460 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43360560 | CAGAAGAAACAGACA[-/G]GGTGATAGGCATCCA | 23072 |
rs36060417 | in-del | -/GTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43389813 | CCTGACTAAATTTTT[-/GTT]GTAGAGAAAGAGTCT | 23072 |
rs36060516 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43474096 | TAATATAGTGTGAAG[A/C]CAATAACAGAAAAAC | 23072 |
rs36062684 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358617 | GATTAAAATTTAATG[-/A]AAAAGTTTAACCCTA | 23072 |
rs36064701 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43528116 | ACCATGAAAGGCTGC[-/G]TTGCCTGGATAACTA | 23072 |
rs36067285 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237906 | CATATCCATGACAGG[-/G]AAAGTTAAATGAGAT | 23072 |
rs36076284 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43420919 | ATCCTGGGAGATATG[-/T]TTAATGTAACTTGAC | 23072 |
rs36081161 | snp | A/G | 0.199254 | 0.244796 | intron-variant | HECW1 | GRCh38.p7 | 7:43341490 | ATGTAAAAAATATAT[A/G]TCAGCTATCACAATT | 23072 |
rs36082509 | snp | A/G | 0.499866 | 0.0081858 | intron-variant | HECW1 | GRCh38.p7 | 7:43342876 | TAAAGATACAAAAAA[A/G]TCAGCTGGTCGTAGT | 23072 |
rs36088559 | in-del | -/AA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43259388 | GTCCAAAAAAAAAAA[-/AA]CCGTTCAATATATAA | 23072 |
rs36093935 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43471820 | AAAATGAGAAGGGGC[C/T]TAGGAAGAGACACTA | 23072 |
rs36094358 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264842 | AGTGAGACTCGGTTT[-/A]AAAAAAAAAAAAAAA | 23072 |
rs36097214 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347687 | CTTTTATTGCACTAA[-/G]GGTATGTTCCTTCTA | 23072 |
rs36101732 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308042 | TTATATATTATATTG[G/T]ATTATATATAATACA | 23072 |
rs36117153 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159678 | CTATTTCCTTGTATC[-/T]TTTTTTTTTTTTTTT | 23072 |
rs36121841 | snp | A/G | 0.493201 | 0.0579089 | intron-variant | HECW1 | GRCh38.p7 | 7:43465400 | CACAGGCTGACCTGA[A/G]ATGGCTGCCACTAGG | 23072 |
rs36136846 | snp | A/G | 0.401392 | 0.198948 | intron-variant | HECW1 | GRCh38.p7 | 7:43237080 | GAGAAGGAGGGAGGG[A/G]GGGAGGAAGCAGGGA | 23072 |
rs36145761 | snp | C/G | 0.180064 | 0.240019 | intron-variant | HECW1 | GRCh38.p7 | 7:43237078 | AGGAGAAGGAGGGAG[C/G]GAGGGAGGAAGCAGG | 23072 |
rs55642652 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43285005 | TGTATGGATTTTTTT[-/T]TTTTTTGCTTTAAGG | 23072 |
rs55650744 | snp | A/G | 0.185788 | 0.241613 | intron-variant | HECW1 | GRCh38.p7 | 7:43455620 | AGTGACAGTGGTGAT[A/G]GACATTTCTAAAGAA | 23072 |
rs55658625 | snp | C/G | 0.188946 | 0.24243 | intron-variant | HECW1 | GRCh38.p7 | 7:43529390 | TGTAACTCACTCTTC[C/G]CCATTCCATGCCAGG | 23072 |
rs55660644 | snp | G/T | 0.335788 | 0.23482 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148856 | AGGGCCTGAGATTTT[G/T]CATTTCTAAGAAGCT | 23072 |
rs55670468 | in-del | -/A | 0.330714 | 0.236612 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131081 | ACCAGCCTGGCCAAT[-/A]ATGGTGAAACCCCAT | 23072 |
rs55674782 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | HECW1 | GRCh38.p7 | 7:43467556 | GGGCTGCCTGACCAG[A/G]GGGGTTGATGATGCA | 23072 |
rs55687362 | snp | A/G | 0.463018 | 0.130857 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248208 | TCACCCAGAGATCGC[A/G]GGGCTGAGGTGGAGC | 23072 |
rs55689100 | snp | C/T | 0.189261 | 0.242509 | intron-variant | HECW1 | GRCh38.p7 | 7:43534346 | CGTTTAAATAATCTG[C/T]TGAAAAATACACTGA | 23072 |
rs55689806 | in-del | -/ATTT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120633 | TTTATTTATTTATTT[-/ATTT]GTTTTATTTTTTGAG | 23072 |
rs55704525 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43528967 | TTATGGGGCATTGGG[A/G]AGGAGATTCTTTACA | 23072 |
rs55713423 | snp | C/G | 0.199254 | 0.244796 | intron-variant | HECW1 | GRCh38.p7 | 7:43328859 | ATTAACCCAAAGTCA[C/G]ACTTTTCTGGATTAA | 23072 |
rs55713548 | snp | A/G | 0.286825 | 0.247273 | intron-variant | HECW1 | GRCh38.p7 | 7:43205905 | CCCTACACTGAGCAC[A/G]GCTGGGCCCCATCTT | 23072 |
rs55735988 | snp | A/G | 0.329317 | 0.237084 | intron-variant | HECW1 | GRCh38.p7 | 7:43250135 | CACACACACACACAC[A/G]CGCACACACACATAC | 23072 |
rs55737556 | snp | C/G/T | 0.00255701 | 0.0356804 | intron-variant | HECW1 | GRCh38.p7 | 7:43541847 | TGTTTGGTAATTTGC[C/G/T]TTTCTCACTGAATTC | 23072 |
rs55764422 | snp | C/T | 0.172351 | 0.237636 | intron-variant | HECW1 | GRCh38.p7 | 7:43399599 | AGGGGACAGTCTCTA[C/T]TCCTTTATCTCTGCT | 23072 |
rs55765018 | snp | A/C | 0.243061 | 0.249904 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131188 | GGAGAATTGCTTGAA[A/C]CCAGGAGCAGAGGTT | 23072 |
rs55784834 | snp | C/T | 0.282632 | 0.247861 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120851 | TTTTCACCATGTTGG[C/T]CAGGCTGGTCTGGAA | 23072 |
rs55810051 | in-del | -/TTATT | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130869 | TGCTCAACCTGTATT[-/TTATT]AATAACTGGGTATAC | 23072 |
rs55810240 | snp | A/G | 0.165853 | 0.235413 | intron-variant | HECW1 | GRCh38.p7 | 7:43390490 | AAGCTGCAGTGAGCT[A/G]TGATGGTGCTACTGC | 23072 |
rs55824258 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43545381 | ACAATCCTCTAGTGT[A/G]AAGTGTAGGAATTCG | 23072 |
rs55825787 | snp | C/T | 0.268724 | 0.249298 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124662 | GGCTGGTGGCATCAA[C/T]GATCGAGGTGCAAAG | 23072 |
rs55835328 | snp | A/C | 0.473359 | 0.112298 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520463 | TGCTCTGCTGCCCAT[A/C]TGTGCGCGATTGTTT | 23072 |
rs55854935 | snp | A/G | 0.164546 | 0.234942 | intron-variant | HECW1 | GRCh38.p7 | 7:43353721 | AGTGAAATGGAGGTA[A/G]ACAACCAGCTTCCAC | 23072 |
rs55860415 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281739 | TTTTTTTTTTTTTTT[-/T]AGAGAGACAAGGTCT | 23072 |
rs55875970 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43354194 | ATAAAAAAAAAAAAA[-/A]GGCCAGACAGAGAAG | 23072 |
rs55881060 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43204348 | AGTAGATTTTGTTCA[A/G]GAAACCCTAAGTCAT | 23072 |
rs55893602 | snp | A/G | 0.19646 | 0.2442 | intron-variant | HECW1 | GRCh38.p7 | 7:43456859 | TACAGTTCTCAAAAG[A/G]ATAGAGACCTCAGTT | 23072 |
rs55897278 | snp | C/T | 0.199254 | 0.244796 | intron-variant | HECW1 | GRCh38.p7 | 7:43328891 | CTTAAGTTGCCAAGT[C/T]GGTGTGAGAACATAA | 23072 |
rs55909267 | snp | C/T | 0.440884 | 0.161442 | intron-variant | HECW1 | GRCh38.p7 | 7:43416925 | GGCCTGCACCCACTG[C/T]CTGGCACTCCCTAGT | 23072 |
rs55919009 | snp | A/G | 0.255782 | 0.249933 | intron-variant | HECW1 | GRCh38.p7 | 7:43464848 | CTCTTTTTCACCCAG[A/G]CTGGAGTGCATGGTG | 23072 |
rs55969907 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | HECW1 | GRCh38.p7 | 7:43276169 | ATGGTAAGAAATGAT[C/T]TTACATAACAACTAT | 23072 |
rs55974790 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43205669 | CAGCATGCCTGGCCA[C/T]GTGCAGTGGTCTCGT | 23072 |
rs55990573 | snp | C/G | 0.237303 | 0.249677 | intron-variant | HECW1 | GRCh38.p7 | 7:43456742 | TATGCCCCTCTCCTG[C/G]GATGTTCACCAAGGA | 23072 |
rs56016010 | snp | A/G | 0.255503 | 0.249939 | intron-variant | HECW1 | GRCh38.p7 | 7:43255321 | AGATTTATTCAGGCC[A/G]GGCCTGGTGGCTCAT | 23072 |
rs56027240 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529548 | TTCCATTTGACTGTC[A/C]CAAAAGCCTCCATCA | 23072 |
rs56027889 | snp | C/T | 0.494976 | 0.0498674 | intron-variant | HECW1 | GRCh38.p7 | 7:43501892 | CAGTATTTTATGACA[C/T]GTGAAAACTGTATGA | 23072 |
rs56040296 | snp | G/T | 0.43655 | 0.16643 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248914 | AGTGACTTAGGGGCC[G/T]CCCTGCCTCCCCTCT | 23072 |
rs56046258 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511560 | GCTCCAAATTTCTGA[A/G]CAAGGGAAACTGGTT | 23072 |
rs56069834 | snp | A/C | 0.494526 | 0.0520291 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141620 | TCTCCTGCCTCAAGC[A/C]TCCTGAGTAGCTGGG | 23072 |
rs56085756 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43455936 | AACCCAGGAGGTGGA[G/T]GTTGCAGTGAGCCAA | 23072 |
rs56093938 | in-del | -/T | 0.332568 | 0.235971 | intron-variant | HECW1 | GRCh38.p7 | 7:43422369 | TTTTGGTTGTTGTTG[-/T]TTTTTTTTTTTTTTG | 23072 |
rs56097842 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | HECW1 | GRCh38.p7 | 7:43226638 | TCCTTGACGAAGCGG[A/G]TGCCAGGGTGGGACT | 23072 |
rs56105653 | snp | A/G | 0.407158 | 0.194426 | intron-variant | HECW1 | GRCh38.p7 | 7:43203619 | CCTGCCACCATACCC[A/G]GCTAATTTTTGTATT | 23072 |
rs56110823 | snp | A/C | 0.184838 | 0.241358 | intron-variant | HECW1 | GRCh38.p7 | 7:43525977 | GAGTATCAATAAATT[A/C]TATTATCTAAAGAAA | 23072 |
rs56111512 | snp | A/G | 0.286301 | 0.24735 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43552233 | TCAGGTTGTAGACTC[A/G]AGGCTGGTGTCCGTG | 23072 |
rs56115393 | in-del | -/GAA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158415 | AGGATCAAGTAATAA[-/GAA]CTTACCCATTATCTC | 23072 |
rs56125132 | snp | G/T | 0.19646 | 0.2442 | intron-variant | HECW1 | GRCh38.p7 | 7:43454082 | TGAGGAATTGAAACA[G/T]GTGATGATAAATTAT | 23072 |
rs56128040 | in-del | -/AGAGTCG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422936 | CCTGGCCGAGAGTCG[-/AGAGTCG]TGGTCTCCAGGATTT | 23072 |
rs56141341 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43188444 | CATCTACACGAAGGC[A/G]TTTTAAAGCTAACTC | 23072 |
rs56156862 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43262309 | GGCTACAAGAAAAAA[-/G]AAAACAATGGCTATA | 23072 |
rs56163858 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149159 | TCTCCCCCTTAAATA[C/T]GTATTGATTACAAAG | 23072 |
rs56168949 | snp | C/T | 0.170408 | 0.236992 | intron-variant | HECW1 | GRCh38.p7 | 7:43169334 | ATGGGGGCTGACCTG[C/T]GCATGGCAGGGTGTG | 23072 |
rs56175109 | snp | A/G | 0.196771 | 0.244268 | intron-variant | HECW1 | GRCh38.p7 | 7:43328567 | GTGGGAAGACAAGAC[A/G]CAGGCGTGCAGTCAC | 23072 |
rs56189247 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | HECW1 | GRCh38.p7 | 7:43173423 | GTGTTAGGAAAGCCA[C/T]CTGATTAAATAAAGT | 23072 |
rs56200413 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, utr-variant-5-prime, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113949 | AGGGGGAGCTGGCAG[A/G]GACACAGGCTGCAGA | 23072 |
rs56206590 | snp | A/G | 0.186737 | 0.241863 | intron-variant | HECW1 | GRCh38.p7 | 7:43195296 | TGTGCACTGCACTGT[A/G]TGTGAGGTCGCACAG | 23072 |
rs56215750 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | HECW1 | GRCh38.p7 | 7:43486567 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 23072 |
rs56225776 | snp | C/T | 0.199564 | 0.24486 | intron-variant | HECW1 | GRCh38.p7 | 7:43328783 | TTCCAGTCAGATACA[C/T]GTCAGATCTTCCCAA | 23072 |
rs56228630 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HECW1 | GRCh38.p7 | 7:43333472 | ATTTATAAAAGTATT[A/G]CTTATTCCCTACAGA | 23072 |
rs56251607 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43180782 | ATGTGCACATTGTTT[A/C]ATGAACAAATCAGGG | 23072 |
rs56255011 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | HECW1 | GRCh38.p7 | 7:43203984 | AAATGGACTCTTTTT[A/G]TCTTACCTAAAGAAT | 23072 |
rs56264666 | in-del | -/CG/CGTGTG | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43361060 | TCTTGTGCGTGCGTG[-/CG/CGTGTG]TGTGTGTGTGTGTGT | 23072 |
rs56302228 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | HECW1 | GRCh38.p7 | 7:43193603 | GCCAGGCTGGTCTTG[A/T]ACTCCTGACCTCAAG | 23072 |
rs56323436 | snp | C/T | 0.48955 | 0.071525 | intron-variant | HECW1 | GRCh38.p7 | 7:43251902 | AGGTAGGTGTAGAAA[C/T]TCAGCAATCGCAAGA | 23072 |
rs56333180 | snp | A/G | 0.379942 | 0.213577 | intron-variant | HECW1 | GRCh38.p7 | 7:43180497 | ACCCACTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 23072 |
rs56336485 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522483 | CACCTCTGTCTCCAG[C/T]CATAAGCGGGCTGCT | 23072 |
rs56337042 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112128 | GTGTAATAGAAAACG[C/T]GGTTTGGGAGCTAGG | 23072 |
rs56347303 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247745 | GAAAGGAAGGAAGGA[A/G]GGAGGGAGGAAGGGA | 23072 |
rs56367292 | snp | A/G | 0.190205 | 0.242744 | intron-variant | HECW1 | GRCh38.p7 | 7:43473670 | GGGAAGATGAGCAGG[A/G]GAAGGAAAGTTATGC | 23072 |
rs56370175 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43530858 | TCCAAATCTGCCCCC[-/C]TCCTAAAATCTATAT | 23072 |
rs56391205 | snp | A/G | 0.494526 | 0.0520291 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141569 | CAATGGCGCAATCTC[A/G]GCTCACCGCGCCTCC | 23072 |
rs56406648 | snp | A/C | 0.0991586 | 0.199366 | intron-variant | HECW1 | GRCh38.p7 | 7:43308424 | ACCTTAAAAGTCATA[A/C]AATTTTATTTGTCAA | 23072 |
rs56408377 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43194491 | AGCCACTCCTACCCC[A/C]AAAAAAGAAAGAAAA | 23072 |
rs56692346 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43528476 | ACACAAGCTAACCAG[A/G]ATGATGGGTCAAAAA | 23072 |
rs56695153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124664 | CTGGTGGCATCAACG[A/G]TCGAGGTGCAAAGTC | 23072 |
rs56714559 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43395839 | TCATATCAGGCAGGT[G/T]GATGTGAATATCCAA | 23072 |
rs56729298 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | HECW1 | GRCh38.p7 | 7:43275622 | ACCTCCCCAAATTAC[A/G]GAGCTGCCTTGAAGC | 23072 |
rs56757698 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43244051 | CCAGCCCAGGAATTA[C/T]CTCAAGTGTGGCTGG | 23072 |
rs56767607 | in-del | -/T | 0.496264 | 0.043057 | intron-variant | HECW1 | GRCh38.p7 | 7:43432146 | TGTTTATTTTATTTC[-/T]TTTTTTTTTTTGAGA | 23072 |
rs56793527 | snp | A/G | 0.187369 | 0.242028 | intron-variant | HECW1 | GRCh38.p7 | 7:43194851 | GGCGCCTGCCCCCAC[A/G]CCTGGCTACTTTTTG | 23072 |
rs56807758 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43222677 | CAAATTATTCAATTA[A/G]TCTGGAAACCTGACA | 23072 |
rs56811536 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43351680 | TTTTTCTTTCTTCTT[-/C]TTTTTTTTTTTTTTT | 23072 |
rs56839027 | in-del | -/AGGGAGCTGCAAGGGCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226701 | TGAGGGGAAAAGGCC[-/AGGGAGCTGCAAGGGCC]TGACCCTCCTGAAAG | 23072 |
rs56858697 | snp | G/T | 0.439918 | 0.162576 | intron-variant | HECW1 | GRCh38.p7 | 7:43304552 | CTGGAGTGCAGTGGC[G/T]CAATCTTAGCTCACT | 23072 |
rs56887396 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43524740 | ACAAGTTCCTACTAG[A/G]GACTGTGGAGACCCA | 23072 |
rs56945504 | snp | C/T | 0.425277 | 0.178263 | intron-variant | HECW1 | GRCh38.p7 | 7:43345803 | CATCATATATATACA[C/T]ACACACACACACACA | 23072 |
rs56999151 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43500170 | CAGTGGCACGATCTC[A/G]GTTCACTGCAACTTC | 23072 |
rs57015152 | snp | A/G | 0.100231 | 0.200173 | intron-variant | HECW1 | GRCh38.p7 | 7:43171168 | GTTTAGAAAAAGTAA[A/G]ATGCTTGACTTTCTT | 23072 |
rs57018487 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125681 | GAGAATTGCTTGAAT[C/T]TGGGAGGCAGAGGTT | 23072 |
rs57034646 | snp | C/T | 0.38555 | 0.210062 | intron-variant | HECW1 | GRCh38.p7 | 7:43370226 | ATCTCACCAAAAATA[C/T]ACAAATGGAAAATTA | 23072 |
rs57045599 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356777 | TGGAAATTAAACTAC[-/A]TGCTCCTGAACAACT | 23072 |
rs57092973 | snp | G/T | 0.128632 | 0.218563 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141046 | ACAGCCATGCGGTGG[G/T]TTAGGACATCAACAG | 23072 |
rs57102081 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43345058 | GAAGTATAGACTCCG[C/T]TCAGCAAAGACTGGA | 23072 |
rs57145831 | snp | A/T | 0.117188 | 0.211804 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159431 | TTAACCATTTATCTC[A/T]TATGCAAATAACTCT | 23072 |
rs57172878 | snp | C/T | 0.261608 | 0.24973 | intron-variant | HECW1 | GRCh38.p7 | 7:43253738 | TGGTGAAACCCCATC[C/T]CTACTAAAAATACAA | 23072 |
rs57192506 | snp | A/T | 0.364609 | 0.222182 | intron-variant | HECW1 | GRCh38.p7 | 7:43267615 | GAAATTAATAAACTA[A/T]AAACAAAATATAGTG | 23072 |
rs57196739 | in-del | -/G/TTG/TTGTTGTTG | 0.429769 | 0.278145 | intron-variant | HECW1 | GRCh38.p7 | 7:43446154 | TTGTTGTTGTTGTTG[-/G/TTG/TTGTTGTTG]GCTATTTTGGCTAAT | 23072 |
rs57208448 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43236292 | TAAGTAATTACTAAA[A/G]TTATTAAGTGATTTG | 23072 |
rs57209616 | snp | A/G | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43194463 | CTAGCAGGTTTTCCA[A/G]TCTTTACCAGAAAGC | 23072 |
rs57214384 | snp | A/G | 0.487995 | 0.0765403 | intron-variant | HECW1 | GRCh38.p7 | 7:43251936 | AGTGTCATTCATCCA[A/G]GCTGGACCCAGTGCT | 23072 |
rs57234163 | in-del | -/CTCTCA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283271 | TATTTGACCTTTTCA[-/CTCTCA]TTATCTCACGAGTGA | 23072 |
rs57273496 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43364837 | GTAGAAAATCACTGT[C/T]AAAGCAAGCTCTTCC | 23072 |
rs57314844 | snp | C/T | 0.4628 | 0.13121 | intron-variant | HECW1 | GRCh38.p7 | 7:43304648 | AGACACGTGTCACCA[C/T]ACATGGCTAATTTTT | 23072 |
rs57331029 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43342552 | TTACTTAATCTTTTT[C/G]AGCATCTGAAGACAT | 23072 |
rs57338562 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43387224 | CCCCCAGCCAGCCCC[G/T]TCCCTTGGGCTGGCT | 23072 |
rs57403678 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43256977 | ACAGAAATCAGGAAA[C/T]AAAAAAGAAAAATGC | 23072 |
rs57414914 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43305510 | TCCTGCCACACGATG[A/G]ATGACCTCAGAATTT | 23072 |
rs57423975 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137952 | ACTTTTTTTTTTTTT[-/T]AAGATTCCGGCCATT | 23072 |
rs57442970 | snp | A/T | 0.117188 | 0.211804 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159145 | TTTATTTTAAAGAGG[A/T]ATTTTTTATTTTTCA | 23072 |
rs57443323 | snp | C/T | 0.493154 | 0.0581045 | intron-variant | HECW1 | GRCh38.p7 | 7:43252027 | GTATCCTCCTCCTGT[C/T]TCTGCTGATTCAACC | 23072 |
rs57474939 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43238137 | ATGGAGTTCTATTAC[A/G]TGTGTTTGCCCACCA | 23072 |
rs57485248 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43290479 | ATAGAGGTCTTGTGA[G/T]TTTTAACCTCAATGC | 23072 |
rs57581985 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356757 | TCAGAAACTACACAA[A/C]CACATGGAAATTAAA | 23072 |
rs57622385 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250134 | CACACACACACACAC[-/AC]GCGCACACACACATA | 23072 |
rs57627873 | in-del | -/TATATATATATATATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429321 | ATATATATATATATA[-/TATATATATATATATA]CATATATGCAGATTC | 23072 |
rs57632050 | in-del | -/TTAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308249 | TAATATATAATATAT[-/TTAT]ATATATTATATGATA | 23072 |
rs57637215 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43254259 | GAAGATCTTTTTTTT[-/C]CCAGTGGAGAATCAA | 23072 |
rs57645139 | in-del | -/GTGTGT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43241656 | TGTGTGTGTGTGTGT[-/GTGTGT]TTAATTAATTGGATC | 23072 |
rs57648935 | snp | C/T | 0.499954 | 0.00479211 | intron-variant | HECW1 | GRCh38.p7 | 7:43252257 | ACCTCTGAGCATCCT[C/T]CCCAGGTTTCTGCCC | 23072 |
rs57682217 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43313606 | CTTCCCATAGTGCTG[A/G]GATTACAGGTGTGAG | 23072 |
rs57720851 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43378908 | AAAAACAAAATAAAA[A/C]ACCCTTTGCGCTTTG | 23072 |
rs57726963 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43234024 | AGCAGGTGAGGAGCA[A/G]CCAGCTTCTCTCCAC | 23072 |
rs57755987 | snp | C/G | 0.29278 | 0.246313 | intron-variant | HECW1 | GRCh38.p7 | 7:43225807 | TTTTTTTTTTTGGGA[C/G]AGGGTCTCACTGTGT | 23072 |
rs57766152 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43558263 | AGATAGAATAAAGGA[A/G]AGGGGAGAATCTTTG | 23072 |
rs57771277 | in-del | -/T | 0.488726 | 0.0742286 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140124 | TGTTTCATATTTTTT[-/T]CCCCATTCACCTTGA | 23072 |
rs57779448 | snp | A/G | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43280411 | ACTCCAAAAAAGGGC[A/G]ATTAAAATGCCGAGT | 23072 |
rs57825626 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | HECW1 | GRCh38.p7 | 7:43380781 | TGATCCACCTGCCTC[A/G]GCCTCCTGAAGTGCT | 23072 |
rs57874835 | in-del | -/AAAAAAAAAAAA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125769 | TCTTAAAAAAAAAAA[-/AAAAAAAAAAAA]GAGTGAGGCATTAAT | 23072 |
rs57900066 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43369798 | GATTAGAGGCAAGGA[C/G]CTTAGCACAGAATAG | 23072 |
rs57924544 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43196911 | TTTTCCCCCTGCCCT[C/T]GAGCCATTTTTTTAA | 23072 |
rs57950981 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412723 | GTTTTTAGTTCTTGC[C/G]ATAGTTTACTGAGAA | 23072 |
rs57953852 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43219111 | CTCTAGCCTTTTAGT[-/A]TGCAAATACAGGGCG | 23072 |
rs57987187 | in-del | -/TG/TGG/TGTG/TGTGTG/TGTGTGTA/TGTGTGTG | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43210477 | GTGTGTGTGTGTGTG[lengthTooLong]GTATTGTTACAGGGC | 23072 |
rs58012450 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356751 | GAAATCTCAGAAACT[A/G]CACAAACACATGGAA | 23072 |
rs58042420 | in-del | -/TT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43347277 | ATTTAATTTTTTTTT[-/TT]GCAGCTATTGTAAAA | 23072 |
rs58113594 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43558142 | TAAGGAGGTGGCAAA[G/T]TTTCTTTACTTTGAA | 23072 |
rs58143947 | snp | A/T | 0.364609 | 0.222182 | intron-variant | HECW1 | GRCh38.p7 | 7:43267609 | TAAGAAGAAATTAAT[A/T]AACTATAAACAAAAT | 23072 |
rs58158952 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | HECW1 | GRCh38.p7 | 7:43388246 | ATGCATTCCTGAATT[A/G]TTTATCTCTTTGTAA | 23072 |
rs58183547 | snp | C/T | 0.291235 | 0.246576 | intron-variant | HECW1 | GRCh38.p7 | 7:43410818 | AGTATTGTTTTATTG[C/T]CTTTTAATGTTTGTA | 23072 |
rs58250489 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43408859 | TACAGTCATAGAAAC[C/T]TGGATTCTAATCCCA | 23072 |
rs58255657 | in-del | -/CACACACA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43345821 | ACACACACACACACA[-/CACACACA]TCATATATATATACA | 23072 |
rs58258475 | snp | C/T | 0.447162 | 0.153712 | intron-variant | HECW1 | GRCh38.p7 | 7:43546088 | TCTAGATCTTCTTCC[C/T]CTTCTGAACCTGGCA | 23072 |
rs58260043 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43306392 | GATTTTTTTTTTTTT[-/T]AAATCCCATTACCCA | 23072 |
rs58269877 | snp | C/G | 0.114036 | 0.209795 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509223 | TGTTTAGAGCAGTGG[C/G]CAGATGTTATGAGGG | 23072 |
rs58270213 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131834 | TGGGAAAGATGTTGT[A/T]TTCCTGATCAGGAGG | 23072 |
rs58293227 | snp | A/G | 0.404035 | 0.196909 | intron-variant | HECW1 | GRCh38.p7 | 7:43199786 | GCTTTTATTTCTCTC[A/G]TGTTCCAGTACCCAC | 23072 |
rs58294963 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112800 | GGCAGCCAGAGCGCA[G/T]CGAGAGCGGGCGGTC | 23072 |
rs58333121 | snp | C/T | 0.441295 | 0.160954 | intron-variant | HECW1 | GRCh38.p7 | 7:43420740 | AGGAATAAATCTAAC[C/T]GCAGAGGAGGAATAT | 23072 |
rs58342021 | snp | C/G | 0.268452 | 0.249318 | intron-variant | HECW1 | GRCh38.p7 | 7:43319130 | CGGTGGCTCACGCCT[C/G]TAATCCCAGCACTTT | 23072 |
rs58394495 | snp | C/T | 0.168135 | 0.236216 | intron-variant | HECW1 | GRCh38.p7 | 7:43330766 | TGGTTTGCTGGAACT[C/T]TCCTGGTTTGGGCCC | 23072 |
rs58417682 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43462676 | CTACTGCAGGGCGCC[C/T]TCTGGGGCTCCCTCT | 23072 |
rs58459680 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356788 | CTACATGCTCCTGAA[C/T]AACTAATGGAGAAAT | 23072 |
rs58487130 | in-del | -/A | 0.349452 | 0.229367 | intron-variant | HECW1 | GRCh38.p7 | 7:43243599 | TGTTTCTTGAAAAAG[-/A]AAAAAAAAAATTCTA | 23072 |
rs58558125 | snp | A/G | 0.219349 | 0.248114 | intron-variant | HECW1 | GRCh38.p7 | 7:43327195 | GACTGAACCCCACCT[A/G]TGCAACGTAAAGGTG | 23072 |
rs58558819 | in-del | -/CTGTCT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343115 | TGTGCTGATCTATCT[-/CTGTCT]AATTCATCAACTCTG | 23072 |
rs58583363 | in-del | -/T | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43193778 | AACAACTGCCTGACC[-/T]TTTGCCTGATGGCTA | 23072 |
rs58597019 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336798 | TACATTAAAGCATGT[-/G]ATGCTTGATTTGCTG | 23072 |
rs58601837 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | HECW1 | GRCh38.p7 | 7:43201219 | TCCTGCTCTCTGGGC[A/G]TGGTGAATTAGAGGA | 23072 |
rs58613719 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43273701 | GGAAAAGAAATCAGG[-/G]ATATTTGACAATATA | 23072 |
rs58625207 | in-del | -/T | 0.460252 | 0.135255 | intron-variant | HECW1 | GRCh38.p7 | 7:43349045 | TTTTGTTTTGTTTTG[-/T]TTTTTTGAGACGGAA | 23072 |
rs58654756 | in-del | -/AACA/AAGA | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43383831 | GCCTTGCCAGTAACA[-/AACA/AAGA]GTTGATTAACATATT | 23072 |
rs58672776 | in-del | -/ATTT | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43409377 | CAAAAGAATTTATTT[-/ATTT]TGTATGGGGGGAAAG | 23072 |
rs58684658 | in-del | -/A | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513656 | AGCTGGAAAAAAAAA[-/A]CTGTTTGTGGGTTTT | 23072 |
rs58692462 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43344373 | TTATGTTGACAGATA[C/T]CTCCTTTCAGCACTT | 23072 |
rs58745413 | snp | A/G | 0.166506 | 0.235645 | intron-variant | HECW1 | GRCh38.p7 | 7:43250952 | CACAACTCCTACTTA[A/G]CTCACCTCCTCTGAA | 23072 |
rs58755780 | in-del | -/T/TT | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135993 | CTTTTTTTTTTTTTT[-/T/TT]ACTATTTGCTGATAG | 23072 |
rs58773073 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43336703 | CCTTTATCCCTCTCC[A/C]AATCTCCCCACTTTT | 23072 |
rs58826071 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43197927 | GGGCCCCTGATTCCC[C/T]GTCAGCTGTGGCTGC | 23072 |
rs58911917 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192549 | AGAAAAAAGTGGTAC[-/A]CTATTGAAGATTCTT | 23072 |
rs58930495 | in-del | -/TAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315491 | TATTATTATTATTAT[-/TAT]CATTATTACTATTAT | 23072 |
rs58946452 | snp | A/T | 0.260504 | 0.249779 | intron-variant | HECW1 | GRCh38.p7 | 7:43474837 | GACACATGCTACAAC[A/T]TGAATGAACCTTGAA | 23072 |
rs59002992 | in-del | -/A | 0.475877 | 0.107142 | intron-variant | HECW1 | GRCh38.p7 | 7:43229634 | AAGTTAAAAAAAAAA[-/A]TTAATGGGCTATAAA | 23072 |
rs59026763 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43218203 | TGCTGGGCCATTCAG[C/T]GTAAGATATATTTAG | 23072 |
rs59038649 | in-del | -/ACCCCACCTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327186 | ACATGAGGAGACTGA[-/ACCCCACCTG]TGCAACGTAAAGGTG | 23072 |
rs59069363 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138527 | CATTTCTGAAGTGTT[G/T]TTATAAAAACGCCTT | 23072 |
rs59097917 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124212 | ACTGTTAGAACTCCT[A/G]CCTTTGAAATTTCAT | 23072 |
rs59118424 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43369759 | TCTTTCTCTGCAGCA[A/G]GGTCCAAATGTTGAC | 23072 |
rs59125324 | snp | G/T | 0.195214 | 0.243923 | intron-variant | HECW1 | GRCh38.p7 | 7:43250839 | TTCTCTTGAAAAAAA[G/T]CAAAAGCTCCTACAG | 23072 |
rs59173315 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43264187 | CAATAGATCTCTAAA[A/T]CTTATTCTAACTGAC | 23072 |
rs59223768 | in-del | -/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514302 | CTTTTTTTTTTTTTT[-/T]GAGATGGAATTTCGC | 23072 |
rs59256596 | in-del | -/C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180064 | TCACAACTGCACTTG[-/C/G]CCAGTTTACGTTATC | 23072 |
rs59257501 | snp | A/G | 0.209693 | 0.246729 | intron-variant | HECW1 | GRCh38.p7 | 7:43164784 | TGGTGCATGTGAGGC[A/G]AGTGCAGACTCTTCC | 23072 |
rs59300763 | in-del | -/C/T | 0.465052 | 0.127485 | intron-variant, upstream-variant-2KB, frameshift-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43113672 | TGCCGGGGCGGGGAG[-/C/T]GGGGGGGGAATGCGT | 23072 |
rs59314738 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494521 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 23072 |
rs59337895 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | HECW1 | GRCh38.p7 | 7:43401179 | CATTATTCTGTCTAC[C/T]GCAGTCAAGAAGAGA | 23072 |
rs59351229 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155490 | AAATTCATCTTATAA[A/G]GAAATTGAGTTTACT | 23072 |
rs59371616 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356750 | AGAAATCTCAGAAAC[C/T]ACACAAACACATGGA | 23072 |
rs59385107 | snp | A/G | 0.119978 | 0.213528 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158559 | AAGGAGCTGGGTACC[A/G]CTTTTTAAAAACTGG | 23072 |
rs59385606 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43411862 | TGCATTGCCTATGGA[C/G]AGCATATTCTTCGGA | 23072 |
rs59398049 | snp | C/G | 0.261332 | 0.249743 | intron-variant | HECW1 | GRCh38.p7 | 7:43207645 | TCCCCGTTCCCTTGT[C/G]AGCTTCTAGTATCCT | 23072 |
rs59427547 | in-del | -/A | 0.330482 | 0.236691 | intron-variant | HECW1 | GRCh38.p7 | 7:43440885 | AACAATTTTTAAGTC[-/A]GGGGCTTGTTGGGAT | 23072 |
rs59438683 | in-del | -/CACA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43345825 | ACACACACACACACA[-/CACA]TCATATATATATACA | 23072 |
rs59469644 | in-del | -/A | 0.100231 | 0.200173 | intron-variant | HECW1 | GRCh38.p7 | 7:43178927 | TCAGAACACTTCCTG[-/A]AAATATCTTTTTTAT | 23072 |
rs59472908 | in-del | -/A | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134415 | AAAAAAAAAAAAAAA[-/A]GAATAAATGTGTTTT | 23072 |
rs59520664 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43364702 | GGCAGGGAAGGAGAC[C/T]TAGTTGTCTTAGGTT | 23072 |
rs59543710 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43178296 | CAGGCGTGAGCCACC[A/G]CACCTGGCCAGCAGG | 23072 |
rs59547891 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43419046 | TCATTTGCCCTGTGC[A/G]TGTATGATTCTGGGA | 23072 |
rs59574736 | snp | A/G | 0.114738 | 0.210248 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508359 | ACAAGAGGATATGCC[A/G]ACAATACAGTCCCAG | 23072 |
rs59580794 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43194711 | CCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 23072 |
rs59607666 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308628 | CATGCCTTTCTGTAA[-/T]TTTTTTTTTTTTTTG | 23072 |
rs59645954 | snp | C/T | 0.116488 | 0.211364 | intron-variant | HECW1 | GRCh38.p7 | 7:43245439 | TTCCTTCTGAGTGCA[C/T]TTCACATTCAGGAAG | 23072 |
rs59685030 | in-del | -/AA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355625 | TAAAAAGCAAAAAAA[-/AA]CATACTACCAGAGAA | 23072 |
rs59715518 | in-del | -/ATTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43330990 | TTTATTTATTTATTT[-/ATTT]TATTTTTTTATATAC | 23072 |
rs59804087 | in-del | -/TATATATATATATATATATATATATATATATATATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429301 | ATGCATATATATATA[lengthTooLong]CATATATGCAGATTC | 23072 |
rs59809720 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43312343 | ACACAAATGTCATTA[A/T]CATTTGCAACTATAG | 23072 |
rs59894337 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303326 | GACAAGGAGCAAAGA[C/T]CACCCCACCCCCCGC | 23072 |
rs59930626 | in-del | -/GAAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283147 | AAAGAAAGAAAGAAA[-/GAAA]TTCTCGGTGTACAGT | 23072 |
rs59937541 | snp | A/G | 0.193653 | 0.243567 | intron-variant | HECW1 | GRCh38.p7 | 7:43186099 | AAGAGCAAGATAATC[A/G]TCATAGAGCTTCTTT | 23072 |
rs60008296 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136071 | TCAACTTTTTTTTTT[-/T]CTCAGTTTATTCACC | 23072 |
rs60013107 | snp | C/T | 0.223522 | 0.248594 | intron-variant | HECW1 | GRCh38.p7 | 7:43547564 | GAAAAAAAAAAAAGC[C/T]GTGTTTTCAATATGA | 23072 |
rs60032315 | in-del | -/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43273871 | CTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTCTC | 23072 |
rs60033220 | snp | C/G | 0.204189 | 0.245767 | intron-variant | HECW1 | GRCh38.p7 | 7:43164827 | GAGATGCCGAGCATG[C/G]AGCCGCGCTTCCATG | 23072 |
rs60045392 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43355297 | ATACTCTAATACTGT[A/T]ATTGTGGTGTGCAAT | 23072 |
rs60086194 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43432241 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 23072 |
rs60103742 | snp | A/G | 0.107694 | 0.205546 | intron-variant | HECW1 | GRCh38.p7 | 7:43371610 | TTAGCAAAATTTATC[A/G]AATTTATCAAAATTT | 23072 |
rs60104224 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413004 | AAATGGTATTTCTAA[A/T]TCTAGATCCCTGAGG | 23072 |
rs60170377 | in-del | -/A/ACTTA | 0.0570934 | 0.159019 | intron-variant | HECW1 | GRCh38.p7 | 7:43348169 | TGTTTGTAATTTTTT[-/A/ACTTA]AATTACCATTTTAAT | 23072 |
rs60274523 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296520 | GGCGGCGCAGCTGTG[A/G]ACGCAGCTGCGGAAG | 23072 |
rs60302967 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43369844 | CACTTTCCCTAAAAC[A/C]AAACGAAATGGATGA | 23072 |
rs60407159 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43409268 | AACACTGATAGCACC[A/G]CTAGAATGGAATAAT | 23072 |
rs60419364 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264863 | AAAAAAAAAAAAAAA[-/A]TTGCTATTGTCGAGA | 23072 |
rs60464522 | snp | G/T | 0.172028 | 0.23753 | intron-variant | HECW1 | GRCh38.p7 | 7:43327184 | CTACATGAGGAGACT[G/T]AACCCCACCTGTGCA | 23072 |
rs60467608 | in-del | -/TGT/TGTTGT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43179582 | TGTTGTTGTTGTTGT[-/TGT/TGTTGT]CGTTTTTGCTGAGAC | 23072 |
rs60509712 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43169097 | GGGAAAGAAATCAAA[-/A]TGCTCTCCCTCAATT | 23072 |
rs60532278 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43432402 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 23072 |
rs60534815 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356758 | CAGAAACTACACAAA[C/T]ACATGGAAATTAAAC | 23072 |
rs60582473 | snp | A/G | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43194733 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 23072 |
rs60586879 | snp | A/C | 0.31503 | 0.241394 | intron-variant | HECW1 | GRCh38.p7 | 7:43362741 | AGGAAGGCACTGAGC[A/C]CACAACAGGCAGAGA | 23072 |
rs60593140 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43308371 | ATATAATATAACATA[A/T]AATATATTTATATAT | 23072 |
rs60618828 | in-del | -/CA/GCACACACACGCGCGC/GCACACACACGCGCGCAC | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302956 | CACACACATGCGCGC[lengthTooLong]ACACACACACACAGG | 23072 |
rs60651990 | in-del | -/AGAT/AGATAGAT/AGATAGATAGATAGAT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43425343 | GATAGATAGATAGAT[lengthTooLong]GCTTTATTGAGCAGT | 23072 |
rs60661398 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43345053 | GCTGTGAAGTATAGA[C/T]TCCGCTCAGCAAAGA | 23072 |
rs60668054 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43500127 | TTTTTTTGAGATGAA[G/T]TCTTCCTCTGTCGCC | 23072 |
rs60696858 | snp | A/G | 0.206947 | 0.246265 | intron-variant | HECW1 | GRCh38.p7 | 7:43165061 | TTTTGGAGAAATGCC[A/G]TAAGTTAGTCTGGCT | 23072 |
rs60732272 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43473989 | ATACCAAAAGGAAAA[-/A]CACTCTCAGCTTTGG | 23072 |
rs60796837 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355986 | GAGCAAGACTCCGTT[A/T]AAAAAATAAATAAAA | 23072 |
rs60834642 | snp | A/G | 0.437542 | 0.165312 | intron-variant | HECW1 | GRCh38.p7 | 7:43416207 | TACAGATGGGTTTTC[A/G]GTGTGGATGTCCTTT | 23072 |
rs60879855 | snp | C/T | 0.106987 | 0.205054 | intron-variant | HECW1 | GRCh38.p7 | 7:43256469 | ACAAAATTAGCCAGC[C/T]GTGGTGGCAGGCGCC | 23072 |
rs60896047 | in-del | -/T/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159193 | ATTTTCTTTTTTTTT[-/T/TT]ATTATTATACTTTAA | 23072 |
rs60938169 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356745 | ACAAGAGAAATCTCA[-/G]AAACTACACAAACAC | 23072 |
rs60946346 | in-del | -/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134731 | GGGGGATTTTTTTTT[-/TT]CTTACTTTAATAAAT | 23072 |
rs60965009 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | HECW1 | GRCh38.p7 | 7:43229017 | TTTCAGATTTTCCAC[A/G]GTACGAATGAATTAT | 23072 |
rs60965036 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | HECW1 | GRCh38.p7 | 7:43411936 | TGAATGGCCCATTAC[C/T]ATTTAACATATTTAT | 23072 |
rs60977844 | snp | A/T | 0.483923 | 0.0882034 | intron-variant | HECW1 | GRCh38.p7 | 7:43378816 | CTCAAAAAACAAAAA[A/T]AAAAACAAAAGAAGG | 23072 |
rs61003857 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43558232 | GTCAGAGTCGAAGTA[C/G]CACTGGGCAGTGTGG | 23072 |
rs61143662 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296808 | GCGGCCTCCACAGCT[C/T]TGCTCCTTGCTGGAA | 23072 |
rs61144684 | snp | A/C | 0.115088 | 0.210473 | intron-variant | HECW1 | GRCh38.p7 | 7:43166465 | ATTAGGATCTAGAAG[A/C]AGCACCCAGGCCAGC | 23072 |
rs61224128 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413023 | AGATCCCTGAGGAAT[C/T]GCCACACTGACTTCC | 23072 |
rs61241516 | in-del | -/TTAT | 0.4582 | 0.138394 | intron-variant | HECW1 | GRCh38.p7 | 7:43304460 | ATTCATTCAACACAG[-/TTAT]TTATTTATTTATTTA | 23072 |
rs61259488 | in-del | -/GTGTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361084 | TGTGTGTGTGTGTGT[-/GTGTGT]ACGTGTACATACACA | 23072 |
rs61275997 | in-del | -/TT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43546242 | TTTTTTTTTTTTTTT[-/TT]GCCATATCCACAGTC | 23072 |
rs61308493 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136823 | ATAGTCAATGCACGT[C/T]CACTCTCACTTGTTC | 23072 |
rs61339934 | in-del | -/CT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161720 | GAACTTCCAAGGTCT[-/CT]GTATCACTAAGGTGA | 23072 |
rs61346880 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121776 | GAGTATCATTATTTG[C/T]TTATTCTTCACTCTC | 23072 |
rs61377628 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347268 | TTTAATTTAATTTAA[A/T]TTTTTTTTTTGCAGC | 23072 |
rs61379617 | snp | C/T | 0.460477 | 0.134905 | intron-variant | HECW1 | GRCh38.p7 | 7:43260315 | ATGTTAAGTAGGCAC[C/T]GAGAAGGGAAGATGT | 23072 |
rs61394694 | in-del | -/AAATTACT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348168 | TTGTTTGTAATTTTT[-/AAATTACT]TAATTACCATTTTAA | 23072 |
rs61397463 | snp | C/T | 0.243919 | 0.249926 | intron-variant | HECW1 | GRCh38.p7 | 7:43494251 | ATCTCCTCTCCTCCC[C/T]CTTCTTCCACCTCCA | 23072 |
rs61442575 | in-del | -/AC/ACAC | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43425248 | CACACACACACACAC[-/AC/ACAC]GTGTACATATATGCA | 23072 |
rs61444685 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289121 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTATCGA | 23072 |
rs61459817 | snp | G/T | 0.117188 | 0.211804 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159358 | CCCCCGACAGGCCCC[G/T]GTGTGTGATGTTCCC | 23072 |
rs61465429 | in-del | -/A | 0.355096 | 0.226837 | intron-variant | HECW1 | GRCh38.p7 | 7:43555915 | GTTAAGTTGAATGAT[-/A]GATTTCAAGAATATA | 23072 |
rs61486109 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454109 | TTATCATTATTGCAG[C/T]TTCATTTTCTAGCTT | 23072 |
rs61489511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159390 | ACCCTGTGTCCAAGT[C/G]ATCTCATTGGAATCT | 23072 |
rs61544473 | snp | A/C | 0.029116 | 0.117091 | intron-variant | HECW1 | GRCh38.p7 | 7:43313388 | TGTTGCACAGGCTGG[A/C]GTTCAGTGGTGCGAT | 23072 |
rs61574015 | snp | G/T | 0.447291 | 0.153545 | intron-variant | HECW1 | GRCh38.p7 | 7:43546090 | TAGATCTTCTTCCCC[G/T]TCTGAACCTGGCACT | 23072 |
rs61598456 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319860 | TCAGGTGATCTTCCC[A/C]CCTCGGCCTCTCAAA | 23072 |
rs61616410 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355993 | ACTCCGTTAAAAAAA[A/T]AAATAAAATGAAATA | 23072 |
rs61633508 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | HECW1 | GRCh38.p7 | 7:43419278 | TTCAGGGCAAAGATC[C/T]CACTGTGAAGAATTC | 23072 |
rs61642321 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43325197 | GTCAATGGCTATAAC[A/G]TGAGAACTCTAAAGA | 23072 |
rs61658804 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523709 | CAAGTGTAGATTGCA[A/G]ATGTACTTACTAATG | 23072 |
rs61683909 | in-del | -/C | 0.0759472 | 0.179459 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111732 | CTTCAGTAAGGAGTT[-/C]TGAAGTCAGGGTGAA | 23072 |
rs61696472 | snp | A/G | 0.494358 | 0.0528145 | intron-variant | HECW1 | GRCh38.p7 | 7:43464229 | TTTTTTCACTTATAA[A/G]TAAAACATGCAATAA | 23072 |
rs61697127 | snp | A/G/T | 0.0777577 | 0.182546 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128026 | AGGAACAACAGGTGC[A/G/T]CACCACCACATTGGG | 23072 |
rs61700075 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | HECW1 | GRCh38.p7 | 7:43201249 | ACACTCCAATGGAAG[A/G]GGCAGTCCCAATCAC | 23072 |
rs61727601 | in-del | -/AATAAATAAATAAATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43341335 | ATAAATAAATAAATA[-/AATAAATAAATAAATA]GTTACAGTGTCATTT | 23072 |
rs61756574 | snp | C/G | 0.280246 | 0.248164 | missense | HECW1 | GRCh38.p7 | 7:43444382 | GGCAGTGTCCCCGAT[C/G]GTCCAGGGAACCAAA | 23072 |
rs61756575 | snp | A/G | 0.0646999 | 0.167821 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444537 | GCCTGCCCCCAGTGC[A/G]GAAGAGCTGGCCGAG | 23072 |
rs61756576 | snp | C/G | 0.00514907 | 0.0504779 | missense | HECW1 | GRCh38.p7 | 7:43444676 | GCTGGAAGGGAAGAA[C/G]AGGAGAAGGAGCAGG | 23072 |
rs61756577 | snp | C/G | 0.002112 | 0.0324275 | missense | HECW1 | GRCh38.p7 | 7:43492135 | CCAGGACACAGCTTA[C/G]TAGCTGCTATTCGAA | 23072 |
rs61756578 | snp | C/T | 0.00360371 | 0.042295 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43541175 | CAGGTTCAGGTTTAG[C/T]GGTCGCATCCTGGGT | 23072 |
rs62458211 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142251 | GGGGGCCCATGGAAT[A/C]GGGCCCCTGGGACTT | 23072 |
rs62458213 | snp | A/G | 0.202959 | 0.245534 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156308 | GCAGGCCCCCAGTAG[A/G]TGTTCACTGAATTAA | 23072 |
rs62458214 | snp | A/G | 0.133777 | 0.221342 | intron-variant | HECW1 | GRCh38.p7 | 7:43169860 | CTCCTCATGATGCCA[A/G]TTCCCCACCCCCAGG | 23072 |
rs62458215 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43173862 | TTTTTTTTTTTTTTG[G/T]AGACAGGGTATCACT | 23072 |
rs62458216 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43201925 | AGAAGTATGACTTAC[A/G]ACTCTGGGGTAGAAT | 23072 |
rs62458218 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43205087 | TCTGAAACAAACAGT[A/T]ATTTTTTTTTTTTGG | 23072 |
rs62458219 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | HECW1 | GRCh38.p7 | 7:43210823 | CCAGAGGGGTGGAAG[C/T]CAGTAGTGGGTCTGC | 23072 |
rs62458220 | snp | C/T | 0.0372196 | 0.131242 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43212973 | ATTATGACAGAAGTA[C/T]ATTTAAAGCATGAGC | 23072 |
rs62458221 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43225805 | TCTTTTTTTTTTTGG[G/T]ACAGGGTCTCACTGT | 23072 |
rs62458222 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43231559 | ACTATGTAGACCTTG[A/G]ATGGTGCCAGAGACA | 23072 |
rs62458223 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43244987 | GCTTCTCCTCTGCCA[C/T]AGGGCCCTGCTGCCT | 23072 |
rs62458224 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43246155 | TAAAAAAAAAAAAAT[A/T]AGCTGGGCATGATGG | 23072 |
rs62458225 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250115 | CAGATTTTTTTTAAC[C/T]AAAACACACACACAC | 23072 |
rs62458226 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43280985 | TTTCCCGTTTTGTTT[G/T]GGGCTGTTTCTCCCC | 23072 |
rs62458227 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43325696 | TCAGGAGTCATTTTC[A/C]ACCTCCGTGCCTTGC | 23072 |
rs62458228 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43330659 | TCACCTGTGGAGGGT[G/T]GCCATGTGGGGGCTA | 23072 |
rs62458229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43335499 | CAGCCATCTGCAAAC[C/G]AGGAAGAGAGCCCTT | 23072 |
rs62458230 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43349507 | TCATTTCTTAGGTCT[A/G]TTAGTAATTGTTTTA | 23072 |
rs62458231 | snp | G/T | 0.317933 | 0.240593 | intron-variant | HECW1 | GRCh38.p7 | 7:43350443 | AGTTTTCCTCAATTA[G/T]TCCCCCAAATGTTTT | 23072 |
rs62458232 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354202 | TAAAAAAAAAAAAAG[A/G]CCAGACAGAGAAGAC | 23072 |
rs62458233 | snp | A/T | 0.285257 | 0.247501 | intron-variant | HECW1 | GRCh38.p7 | 7:43355528 | AGTTGTCATCTCCTT[A/T]AAATAACTTGTTACA | 23072 |
rs62458234 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360233 | TTTTTTTTTTTTTAA[A/T]TGGAGTCTCACCCTA | 23072 |
rs62458235 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43366641 | GTCTTGAGCCCTTGT[G/T]CTTGGCAGAGATTAA | 23072 |
rs62458237 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43374671 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 23072 |
rs62458239 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43388412 | ATCTAAAATGCCATG[C/G]ACTTTCAGACCAACC | 23072 |
rs62458240 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43398653 | TTGTAACCACCCAAT[A/G]TGTTCACCTTGCCCA | 23072 |
rs62458241 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43400329 | TATCAAAAATTTGCT[A/C]CATGCTGGTCAGCTC | 23072 |
rs62458242 | snp | C/T | 0.344592 | 0.231414 | intron-variant | HECW1 | GRCh38.p7 | 7:43405097 | TTTCTCTTTCTTGTA[C/T]TAAGGATATAATCTC | 23072 |
rs62458243 | snp | A/G | 0.391769 | 0.205917 | intron-variant | HECW1 | GRCh38.p7 | 7:43405290 | CTCTAATAAGTCAGG[A/G]TCTCCAAGATCACCC | 23072 |
rs62458244 | snp | A/G | 0.344147 | 0.231595 | intron-variant | HECW1 | GRCh38.p7 | 7:43405361 | CATCTAGATATACTC[A/G]TGGTATGACTTATTA | 23072 |
rs62458247 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413931 | TAGGATTGACTTGGC[A/G]ATGCGGGCTCTTTTT | 23072 |
rs62458249 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43414852 | CTGCTGCTGGATTCG[A/G]TTTACCAGTATTTTA | 23072 |
rs62458251 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43425287 | CATGTGGATAGCTAG[A/G]TAGATAGATAGATAG | 23072 |
rs62458253 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43456901 | AAGGATAGGTTCCAT[A/G]AGAAAACTAAAAGCT | 23072 |
rs62458254 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43470615 | TGAGGGAATTTCTGA[C/T]AAGACCTCTTCCCCC | 23072 |
rs62458255 | snp | A/G | 0.172351 | 0.237636 | intron-variant | HECW1 | GRCh38.p7 | 7:43495221 | TGCACCCATCAACCC[A/G]TCATCTACATTAGGT | 23072 |
rs62458256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43503173 | TGTGCAATGCTTGCT[A/G]CCTCTGACGCACAAC | 23072 |
rs62458257 | snp | A/G | 0.5 | 0 | missense | HECW1 | GRCh38.p7 | 7:43507250 | GGTCAGGGTCCGGGG[A/G]AAATTAAGTGAGTGC | 23072 |
rs62458258 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513655 | CACGTTAAGTAAGCT[A/G]GAAAAAAAAACTGTT | 23072 |
rs62458259 | snp | A/G | 0.180702 | 0.240204 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521736 | AAAAATTAGCCAGGC[A/G]TGGTGGCACATGTCT | 23072 |
rs62461060 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43527051 | ACTTTAGTTATCCAG[A/G]CAAGCAGCCTTTTAT | 23072 |
rs62461061 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43527545 | GATTAGGGCCCACCT[G/T]GATAATCCAAGATCA | 23072 |
rs62461063 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43547550 | GACTCTGGCTCAAAG[A/G]AAAAAAAAAAAGCTG | 23072 |
rs62461064 | snp | A/G | | | synonymous-codon | HECW1 | GRCh38.p7 | 7:43552263 | GTTTGATGCCAGGGA[A/G]CTGGAGCTGGTGATA | 23072 |
rs66483006 | in-del | -/CATGTATACA | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43372433 | TTACATATGTATACA[-/CATGTATACA]TGTGCCATGTTGGTG | 23072 |
rs66542816 | snp | C/T | 0.476574 | 0.105661 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248110 | GAGGGAAGAGAAAGA[C/T]AAAGGAGAGGAGGAG | 23072 |
rs66568842 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316805 | CTCCTCTCCTCTCCC[C/G]TCCCGTCTCCTCCCC | 23072 |
rs66611211 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43539674 | CTCTAAGTGCGGAAC[-/G]CACGGGCCCATCACC | 23072 |
rs66650470 | in-del | ATTAT/GAATTAC | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43185420 | GTCGGAACTGTCTCA[ATTAT/GAATTAC]AGGTGACAGCCTGCT | 23072 |
rs66693536 | snp | C/T | 0.344815 | 0.231323 | intron-variant | HECW1 | GRCh38.p7 | 7:43278259 | CATGTCAGTGAACAG[C/T]GATTCCCTCCTTCCT | 23072 |
rs66731189 | in-del | -/ATGTATACAC | 0.484701 | 0.0861117 | intron-variant | HECW1 | GRCh38.p7 | 7:43372424 | GCAGGTTTGTTACAT[-/ATGTATACAC]ATGTATACATGTGCC | 23072 |
rs66739601 | in-del | -/T | 0.334182 | 0.235401 | intron-variant | HECW1 | GRCh38.p7 | 7:43182926 | TTTCCTAGAAATAGA[-/T]TTTTTTTTGGTAGCT | 23072 |
rs66785972 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | HECW1 | GRCh38.p7 | 7:43354190 | CATATCCAATAATAA[A/T]AAAAAAAAAAGGCCA | 23072 |
rs66803540 | in-del | -/TC | 0.461037 | 0.134028 | intron-variant | HECW1 | GRCh38.p7 | 7:43441552 | CGTGTCTTTTTTTAT[-/TC]TCTCTCTCTCTCTGT | 23072 |
rs66828392 | snp | A/T | 0.0829062 | 0.185956 | intron-variant | HECW1 | GRCh38.p7 | 7:43293459 | GCAGTGCAGACAAGG[A/T]CAAAGGGAGTAGCCT | 23072 |
rs66838568 | in-del | -/G/TG | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111411 | CTAAGGTTTGAAAAT[-/G/TG]GGTCTGCTTTGAGCT | 23072 |
rs66881334 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | HECW1 | GRCh38.p7 | 7:43277671 | GTCATCTCCCACTTC[C/T]TTCTCCATTTACCAC | 23072 |
rs66884992 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159191 | TTGTTCATTTTCTTT[-/T]TTTTTTATTATTATA | 23072 |
rs66910107 | in-del | -/AA | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43374797 | AAAAAAAAAAAAAAA[-/AA]CATAGAGAAATATAA | 23072 |
rs66910108 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43374797 | AAAAAAAAAAAAAAA[A/C]ATAGAGAAATATAAT | 23072 |
rs66970073 | snp | A/G | 0.431325 | 0.172108 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301890 | AAAAAAAAAAAAAAA[A/G]GAAGCAGGAGAATAA | 23072 |
rs66974904 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | HECW1 | GRCh38.p7 | 7:43361811 | GAAATAAAAAAGACT[A/C]TCTCTTTTTTTTTTT | 23072 |
rs66978075 | in-del | -/TC | 0.4944 | 0.0526182 | intron-variant, splice-donor-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161717 | GGTGAACTTCCAAGG[-/TC]TCTGTATCACTAAGG | 23072 |
rs67021322 | in-del | -/T | 0.342806 | 0.232136 | intron-variant | HECW1 | GRCh38.p7 | 7:43276454 | CTACATTTTAAAAAA[-/T]ATATAGGTAATAAGA | 23072 |
rs67075006 | snp | C/T | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43195825 | CCAAGGGGTGGAATA[C/T]TCATGAAAATTCCTG | 23072 |
rs67151003 | snp | C/T | 0.0505692 | 0.150756 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359265 | ACTGCATAGGTGTTA[C/T]TCTGCCAGGGAGGCT | 23072 |
rs67182723 | snp | A/G | 0.407674 | 0.194008 | intron-variant | HECW1 | GRCh38.p7 | 7:43246091 | ATCACTTGACGCCAC[A/G]AGTATGAGACCAGCC | 23072 |
rs67210625 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | HECW1 | GRCh38.p7 | 7:43294374 | GTTCCCATGGGGGGA[A/G]GGGGGAGGATGAGAG | 23072 |
rs67330337 | in-del | -/AG/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43553689 | AAAAAAAAAAAAAAG[-/AG/G]TCTCTGCCTGGCTGT | 23072 |
rs67376636 | in-del | -/AGTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224668 | TACAGAAAATAAAAA[-/AGTT]GCCGGCCATGGTGGC | 23072 |
rs67392091 | snp | C/G | 0.103082 | 0.202275 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268806 | TAACAAGATCTTGCT[C/G]TGTCACCCAGGCTGG | 23072 |
rs67460979 | multinucleotide-polymorphism | CGG/GGA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43237080 | AGGAGAAGGAGGGAG[CGG/GGA]GGGAGGAAGCAGGGA | 23072 |
rs67470745 | in-del | -/TATTA | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43180376 | TTCTAAGTTTTATTT[-/TATTA]TTTTATTTTTTTATT | 23072 |
rs67487907 | snp | C/G | 0.408017 | 0.193729 | intron-variant | HECW1 | GRCh38.p7 | 7:43246279 | CTGCATTCCAGCCTG[C/G]GTGACGTAGCAAGAC | 23072 |
rs67518120 | in-del | -/ATAAATAAATAAATAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43341308 | AGAACTTACAGTATT[-/ATAAATAAATAAATAA]ATAAATAAATAAATA | 23072 |
rs67523650 | snp | A/G | 0.346147 | 0.230772 | intron-variant | HECW1 | GRCh38.p7 | 7:43272942 | CATCAGTTGTGGACT[A/G]AATAAAGAAAATGTG | 23072 |
rs67527962 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43555916 | TTAAGTTGAATGATG[-/A]ATTTCAAGAATATAG | 23072 |
rs67534831 | in-del | -/A | 0.0479149 | 0.147179 | intron-variant | HECW1 | GRCh38.p7 | 7:43373176 | TGGTGCTGCCCATGC[-/A]CGTTGGTGTCGTTCT | 23072 |
rs67678899 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544597 | TTGACTCAGCACACG[-/AT]TCTAGAAATTTGTCC | 23072 |
rs67705251 | in-del | -/ATATATATATATATATAT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43429290 | CCATATATTATATGC[-/ATATATATATATATATAT]ATATATATATATATA | 23072 |
rs67718388 | snp | G/T | 0.089084 | 0.191327 | intron-variant | HECW1 | GRCh38.p7 | 7:43407069 | GTACATGGTCAGATA[G/T]CTTCAATTAAACAGA | 23072 |
rs67732910 | snp | C/G | 0.225005 | 0.248747 | intron-variant | HECW1 | GRCh38.p7 | 7:43363952 | AGCCTTTGCAGTCTC[C/G]TCTGGGGACTTGAGC | 23072 |
rs67747013 | snp | C/T | 0.4582 | 0.138394 | intron-variant | HECW1 | GRCh38.p7 | 7:43411100 | TTGCTTTTAGACTTA[C/T]ATTTATTCTCTAATA | 23072 |
rs67887362 | snp | A/C | 0.18989 | 0.242666 | intron-variant | HECW1 | GRCh38.p7 | 7:43196641 | CTCTGCACACTTCTG[A/C]CCTGAGCGGGAGATG | 23072 |
rs68053238 | snp | A/G | 0.101301 | 0.200969 | intron-variant | HECW1 | GRCh38.p7 | 7:43278590 | GGCCTCCGAGGCTCT[A/G]TGTGATCTGATCCCC | 23072 |
rs68122074 | in-del | -/TTAAG | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43456636 | GAGGCGAGAGACAAG[-/TTAAG]CTTGAGTGTCATTTA | 23072 |
rs68143123 | snp | A/G | 0.343924 | 0.231686 | intron-variant | HECW1 | GRCh38.p7 | 7:43287721 | AGACCTGATAGACCA[A/G]GTAAGAGATACTGGT | 23072 |
rs68172320 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440886 | ACAATTTTTAAGTCG[-/A]GGGCTTGTTGGGATA | 23072 |
rs68183123 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | HECW1 | GRCh38.p7 | 7:43403647 | GGGATATTGTTTCCC[A/G]GGCTCTCACATATAA | 23072 |
rs71008891 | in-del | -/TT | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126081 | TTTTTTTTTTTTTTT[-/TT]TTGGTTTTTACTCAC | 23072 |
rs71008892 | in-del | -/AAAA | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127546 | AAAAAAAAAAAAAAA[-/AAAA]GGAAAACAAACAGCC | 23072 |
rs71008893 | in-del | -/ATTT/ATTTATTT | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137567 | TTTATTTATTTATTT[-/ATTT/ATTTATTT]GAGACAGGGTCTTGC | 23072 |
rs71008894 | in-del | -/GTT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43190106 | GTTGTTGTTGTTGTT[-/GTT]TGTTTGCTTTGTTTG | 23072 |
rs71008895 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43192547 | AAGAAAAAAGTGGTA[-/A]CACTATTGAAGATTC | 23072 |
rs71008897 | in-del | -/TTTTTTTTTTTTT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43221567 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTT]GGGACAGCCTGTTGC | 23072 |
rs71008898 | in-del | -/GGTA | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43237188 | GTAGGTAGGTAGGTA[-/GGTA]AAGTGTGACTGTTTG | 23072 |
rs71008900 | in-del | -/TA | 0.0858192 | 0.188533 | intron-variant | HECW1 | GRCh38.p7 | 7:43307877 | TGGTAATCATTTCAC[-/TA]TATATATATATATAT | 23072 |
rs71008901 | in-del | -/TCCTCTCCTCTCCCGTCCCGTCTCCTC | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316791 | TCCCCTCCCCTCCTC[-/TCCTCTCCTCTCCCGTCCCGTCTCCTC]CCCTCTACTCTCTTC | 23072 |
rs71011904 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43336145 | CTCTCTCTCTCTCTT[-/T]CTCTCTCTCTCTCTC | 23072 |
rs71011911 | in-del | -/A | 0.494057 | 0.0541878 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375890 | ATGAGACCCTTCTCA[-/A]AAAAAAAAAAAAAAA | 23072 |
rs71011918 | in-del | -/A | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43457774 | TCAAAAAAAAAAAAA[-/A]CAAACAAAAAACATG | 23072 |
rs71011920 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43530137 | TTTTTTTTTTTTTTT[-/T]AGTAGAGATGGGGTT | 23072 |
rs71011921 | in-del | -/TGGA | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43530534 | GGATGGATGGATGGA[-/TGGA]AAGACAGATATAATT | 23072 |
rs71011922 | in-del | -/GGTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43533621 | GATGCCATAGTGGTT[-/GGTT]AGAAGAGGCCTTTAT | 23072 |
rs71011923 | in-del | -/AT | 0.499087 | 0.0213463 | intron-variant | HECW1 | GRCh38.p7 | 7:43544596 | TTTGACTCAGCACAC[-/AT]GTCTAGAAATTTGTC | 23072 |
rs71011926 | in-del | -/C | 0.492582 | 0.0604491 | intron-variant | HECW1 | GRCh38.p7 | 7:43551972 | TCTCATATCTAAGCA[-/C]CCCCCCAAAGGCCCC | 23072 |
rs71217165 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43361841 | TTTTTTTTTTTTTTT[A/T]ACATTAAAAAAAAAA | 23072 |
rs71296596 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376869 | GTCTCAAAAAAAAAA[-/A]GACATTTCAAATATA | 23072 |
rs71531078 | multinucleotide-polymorphism | CA/TC | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43454838 | AAGCTATGGCTTTTC[CA/TC]ACTGAAAAGGCTGGA | 23072 |
rs71533220 | in-del | CGC/TG | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159766 | GCTCACTGCAAGCTC[CGC/TG]CTCCCAGGTTCATGC | 23072 |
rs71533221 | multinucleotide-polymorphism | AAAT/GAAA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43325817 | TCGTTTCCTCGTGTG[AAAT/GAAA]CCTGGCTGGATGCAC | 23072 |
rs71533222 | multinucleotide-polymorphism | CAC/TAT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43429335 | ATATATATATATATA[CAC/TAT]ACATATATGCAGATT | 23072 |
rs71537737 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43345805 | TCATATATATACACA[C/T]ACACACACACACACA | 23072 |
rs71540509 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43207531 | TATAATATATTACTG[G/T]TAATTGTAGTCATCT | 23072 |
rs71540510 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43208263 | CTTCTATTGATTTCT[A/C]TATTTCAATGGCTAG | 23072 |
rs71540511 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43251730 | CAGCCGATGCTCTGG[G/T]TATTTCCTCTTTTCT | 23072 |
rs71540512 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43263359 | AATCTGAGCTCTGTT[G/T]GTTGTTGTTGTTGTT | 23072 |
rs71540513 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43284420 | GCCTATAATCCTAGC[A/C]ATTTAGGAGGCCAAG | 23072 |
rs71540514 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316814 | CTCCTCCCCTCCCCT[A/C]CTCCCCTCTACTCTC | 23072 |
rs71540515 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316824 | CCCCTCCTCCCCTCT[A/C]CTCTCTTCTTTCCTC | 23072 |
rs71540516 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316830 | CTCCCCTCTACTCTC[C/T]TCTTTCCTCTCATCT | 23072 |
rs71540517 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316851 | CCTCTCATCTCCTGT[C/G]CCTTCCCCTAGTGCA | 23072 |
rs71540518 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316854 | CTCATCTCCTGTGCC[C/T]TCCCCTAGTGCAGAA | 23072 |
rs71540519 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43320009 | GTAAGCTTTGGTTCA[A/G]AAGAGACCATACTGG | 23072 |
rs71540520 | snp | C/T | 0.170733 | 0.237101 | intron-variant | HECW1 | GRCh38.p7 | 7:43330005 | GAGGAGAGTTGAGGA[C/T]GGAATTCCATCGAGG | 23072 |
rs71540521 | snp | C/T | 0.176861 | 0.239062 | intron-variant | HECW1 | GRCh38.p7 | 7:43332422 | GCACAGGCCACATTC[C/T]TGAAATGGGGCCTTG | 23072 |
rs71540522 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HECW1 | GRCh38.p7 | 7:43343565 | AATGATGTTTTCCAG[C/T]TTCATCCATGTCCCT | 23072 |
rs71540523 | snp | G/T | 0.177182 | 0.23916 | intron-variant | HECW1 | GRCh38.p7 | 7:43346763 | CATCCTTTCCCCACT[G/T]TATGTTTTTGTTTGC | 23072 |
rs71540525 | snp | C/T | 0.164546 | 0.234942 | intron-variant | HECW1 | GRCh38.p7 | 7:43355979 | GGCAACAGAGCAAGA[C/T]TCCGTTAAAAAAATA | 23072 |
rs71540526 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | HECW1 | GRCh38.p7 | 7:43356930 | TAGCATCTTTTAAAA[G/T]ATGTGAATAGACATT | 23072 |
rs71540527 | snp | A/G | 0.167809 | 0.236103 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359826 | TGTTTCAAACAAAAT[A/G]TAAGGGACCAAGACA | 23072 |
rs71540529 | snp | A/C | 0.164219 | 0.234823 | intron-variant | HECW1 | GRCh38.p7 | 7:43369987 | GACAAATGGGCCAGA[A/C]CCTAAAGTCAGTTTT | 23072 |
rs71540530 | snp | C/G | 0.084728 | 0.187577 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376380 | AAATAAGTATAGCAA[C/G]TCTCCCTGGGATGGG | 23072 |
rs71540531 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43396440 | AAATACATTATAATT[A/C]CAATAGTAAACATCT | 23072 |
rs71540533 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43422451 | CACTGCAACCTCCGT[C/T]TCTTGGGTTCCAGCA | 23072 |
rs71540534 | snp | A/G | 0.5 | 0 | missense | HECW1 | GRCh38.p7 | 7:43463772 | GGAGGGAGTGACTCA[A/G]AAGCCGAATCTTCCC | 23072 |
rs71540535 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43525235 | TTTAGGCTTGACTCT[A/T]AGTATGAAAATTAAC | 23072 |
rs71540536 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43532256 | GAATACATCCAGACT[C/T]TGACCTCCTCACCTC | 23072 |
rs71540537 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43551349 | GAAGAGAAGGAAAAG[A/C]CAAATTTCCACCCAG | 23072 |
rs71562078 | in-del | -/AAAA | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127524 | GTGAAACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 23072 |
rs71562081 | in-del | -/AC | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43189385 | GGACATTGCTGGTCC[-/AC]AGATTACACAGTGAA | 23072 |
rs71562084 | in-del | CC/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316767 | CCTCTCCCCTCCCCT[CC/T]TTCTCTCCTCCCCTC | 23072 |
rs71562085 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316777 | CCCTTTTCTCTCCTC[-/T]CCCTCCCCTCCTCCC | 23072 |
rs71562086 | in-del | -/G/TCA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316780 | TTTTCTCTCCTCCCC[-/G/TCA]TCCCCTCCTCTCCTC | 23072 |
rs71562088 | in-del | -/A | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43331592 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 23072 |
rs71562089 | in-del | -/ATAA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43341307 | AGAACTTACAGTATT[-/ATAA]ATAAATAAATAAATA | 23072 |
rs71562090 | in-del | -/AT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43345791 | GTGTAGTATTCCATC[-/AT]ATATATATATACACA | 23072 |
rs71562092 | in-del | -/CA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43345828 | ACACACACACACACA[-/CA]TCATATATATATACA | 23072 |
rs71562093 | in-del | -/A | 0.492727 | 0.0598633 | intron-variant | HECW1 | GRCh38.p7 | 7:43355030 | GGAAAAAAAAAAAAA[-/A]CTGCCTCCCAGGAAT | 23072 |
rs71562094 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43373201 | GTTCTGCCTTCTTCC[-/T]TTTTTTTTTTTTTTT | 23072 |
rs71562095 | in-del | -/CAAA | 0.0471551 | 0.14613 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376112 | CATAACCCAATAAAC[-/CAAA]CATATACTCACCTAT | 23072 |
rs71562097 | in-del | -/CA/CACA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43425225 | ATTTACCAAGACACT[-/CA/CACA]CACACACACACACAC | 23072 |
rs71562098 | in-del | -/GATAGATAGATAGAT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43425289 | GTGGATAGCTAGGTA[-/GATAGATAGATAGAT]GATAGATAGATAGAT | 23072 |
rs71562099 | in-del | -/A/GAT/GATA/GATAGATA/GATAGATAGATA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43425304 | GATAGATAGATAGAT[lengthTooLong]GATAGATAGATAGAT | 23072 |
rs71562100 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43431833 | CCCATGGCACCCCTC[-/T]TACCTGGAATGTTCC | 23072 |
rs71562102 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43469339 | TCCTAGCCCTCACGC[CA/TG]CTAGATGCCAACTGT | 23072 |
rs71563903 | in-del | -/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43483704 | AGGCGTGCACCACCA[-/C]CACCTGTTTAATTTT | 23072 |
rs71563904 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43530117 | ACCATGCTTGGCTAA[-/T]TTTTTTTTTTTTTTT | 23072 |
rs71563905 | in-del | -/TGA | 0.447291 | 0.153545 | intron-variant | HECW1 | GRCh38.p7 | 7:43546093 | ATCTTCTTCCCCTTC[-/TGA]ACCTGGCACTGGTTC | 23072 |
rs71649034 | in-del | -/T | 0.494733 | 0.0510469 | intron-variant | HECW1 | GRCh38.p7 | 7:43287647 | TGATTTAGGTTTTTT[-/T]AAAGGTTTCTCTGGC | 23072 |
rs71664866 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43343649 | GATAGACTGGATTAA[A/G]AAAATGTGGCACATA | 23072 |
rs71717961 | in-del | -/CT/TC | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132535 | GAACAAGAGTTTCCT[-/CT/TC]TCTCTCTCTCTCTTT | 23072 |
rs71837963 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210470 | TGTGTGTGTGTGTGT[-/AT]GTGTGTGGTATTGTT | 23072 |
rs72022041 | in-del | -/CA | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43189384 | GGGACATTGCTGGTC[-/CA]CAGATTACACAGTGA | 23072 |
rs72094084 | in-del | -/TTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179555 | TGTTGTTGTTGTTGT[-/TTG]TGTTGTTGTCGTTTT | 23072 |
rs72207857 | in-del | -/TTAAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43230898 | TTTAAAAAAAATAAA[-/TTAAA]GCAGAAAGGGACTGT | 23072 |
rs72213725 | in-del | -/GG | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126090 | TTTTTTTTTTTTTTT[-/GG]TTTTTACTCACCACT | 23072 |
rs72259446 | in-del | -/A | 0.338523 | 0.233803 | intron-variant | HECW1 | GRCh38.p7 | 7:43255597 | AGTGAAACTCTGTCT[-/A]AAAAAAAAAAAAAAA | 23072 |
rs72365480 | in-del | -/TCTCTG | 0.474417 | 0.110168 | intron-variant | HECW1 | GRCh38.p7 | 7:43343112 | GGCTGTGCTGATCTA[-/TCTCTG]TCTAATTCATCAACT | 23072 |
rs72562943 | in-del | -/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43209183 | TGGCATCAGACCCAC[-/G/T]TAGCCCCTCACAATC | 23072 |
rs72585557 | snp | G/T | 0.0839998 | 0.186933 | intron-variant | HECW1 | GRCh38.p7 | 7:43177057 | AACTACTCCTCTAGA[G/T]TTTCAGGGTTGAAAA | 23072 |
rs72585558 | snp | A/G | 0.100231 | 0.200173 | intron-variant | HECW1 | GRCh38.p7 | 7:43177063 | TCCTCTAGAGTTTCA[A/G]GGTTGAAAATTGCCT | 23072 |
rs72585562 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43183496 | GTAAACATTTAAAAC[C/T]TGACAATTTTTGAAA | 23072 |
rs72585564 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | HECW1 | GRCh38.p7 | 7:43185078 | AACATGAAATTTGTG[G/T]GGGGATGCAGATGCA | 23072 |
rs72585569 | snp | A/G | 0.102014 | 0.201495 | intron-variant | HECW1 | GRCh38.p7 | 7:43201441 | AGGAAGGATGCCCAG[A/G]AGTCAAATTGAGAAT | 23072 |
rs72585570 | snp | A/C | 0.100588 | 0.200439 | intron-variant | HECW1 | GRCh38.p7 | 7:43201978 | AGCTTCAGAGAAATT[A/C]ATAATAAGGAGACTT | 23072 |
rs73092821 | snp | A/T | 0.100588 | 0.200439 | intron-variant | HECW1 | GRCh38.p7 | 7:43305719 | GATTCTCCCTGCCAC[A/T]GCTTCAGCAGCTGCG | 23072 |
rs73092824 | snp | A/G | 0.188631 | 0.242351 | intron-variant | HECW1 | GRCh38.p7 | 7:43306395 | TTTTTTTTTTTTTAA[A/G]TCCCATTACCCACCT | 23072 |
rs73092835 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | HECW1 | GRCh38.p7 | 7:43315137 | GACATAAGAGGGGGA[A/G]GATACCTGGATGTAG | 23072 |
rs73092850 | snp | G/T | 0.455858 | 0.141853 | intron-variant | HECW1 | GRCh38.p7 | 7:43323305 | AAGTATTATTAGAAA[G/T]ACATTATAGGCCGGG | 23072 |
rs73092851 | snp | A/G | 0.141934 | 0.225437 | intron-variant | HECW1 | GRCh38.p7 | 7:43323410 | ACCAACCTGGGCAAT[A/G]TGGAAAAACCCCATC | 23072 |
rs73092853 | snp | G/T | 0.0818113 | 0.184966 | intron-variant | HECW1 | GRCh38.p7 | 7:43325770 | CCCACCTCACCTCCC[G/T]GGTCAGTCTTAGGCT | 23072 |
rs73092854 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | HECW1 | GRCh38.p7 | 7:43325956 | TCTGTCTCAGTCCGT[A/T]GAGGCTGTTATAACA | 23072 |
rs73092856 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | HECW1 | GRCh38.p7 | 7:43327063 | TAAGGACTGCACCGC[A/G]GGCTGCCATTTTCAA | 23072 |
rs73092857 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43327352 | CAAGACTCCCCCCAC[C/T]GCTGCCCACCCACTT | 23072 |
rs73092859 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43328319 | AAAACAAAAAACAAA[A/C]AACAAAAAAAACAAG | 23072 |
rs73097343 | snp | C/G | 0.0966517 | 0.197444 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120878 | GGAACTCCTGGCCTC[C/G]AGTGATCTGCAAATC | 23072 |
rs73097353 | snp | C/T | 0.340559 | 0.233022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126507 | CAGAGACCATTAGAC[C/T]CACAAAACCTTAAAT | 23072 |
rs73097355 | snp | C/T | 0.112631 | 0.208878 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128665 | ATTATTTAAGAAATA[C/T]ATTTCTTGATGCTAT | 23072 |
rs73097357 | snp | A/T | 0.030665 | 0.119967 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130764 | TGGCACATGAGGTCC[A/T]TTGTGGAATTTTCCA | 23072 |
rs73097362 | snp | A/G | 0.112631 | 0.208878 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132663 | GCTCAAATTAACCCA[A/G]TTTTGCCCAGTGAGT | 23072 |
rs73097369 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135161 | GGGCCACGACTTAAT[C/T]TGGGAATGGTCTCTT | 23072 |
rs73097383 | snp | G/T | 0.107341 | 0.205301 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152583 | TGCTTTGTTGTTGTT[G/T]TTTTTGTTAGTTTTC | 23072 |
rs73097386 | snp | C/T | 0.106987 | 0.205054 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153696 | ACTTAGTTGTCCAGA[C/T]GTCATTTTCCTGAGG | 23072 |
rs73097651 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | HECW1 | GRCh38.p7 | 7:43344597 | ACCTTGATGTCTTTC[A/G]ATGTAGCACCATCAT | 23072 |
rs73097676 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43357119 | GGGGAGCCCTCATAC[A/G]CTGCTGGTGGGAATG | 23072 |
rs73097683 | snp | C/T | 0.21695 | 0.247806 | intron-variant | HECW1 | GRCh38.p7 | 7:43358158 | GAGGCCATTTGGCCC[C/T]TCCATGCTGATCCCA | 23072 |
rs73098706 | snp | C/T | 0.474861 | 0.109258 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444711 | GGAGGGAGATGTGTC[C/T]ACCCTGGAGCAGGGA | 23072 |
rs73098708 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | HECW1 | GRCh38.p7 | 7:43446154 | TACTGTTGGTTTTGT[G/T]TTGTTGTTGTTGTTG | 23072 |
rs73098710 | snp | A/G | 0.269267 | 0.249256 | intron-variant | HECW1 | GRCh38.p7 | 7:43448818 | GGAATTTAAAACGAC[A/G]TTGCTTGCTTTTAGC | 23072 |
rs73098717 | snp | A/G | 0.259951 | 0.249802 | intron-variant | HECW1 | GRCh38.p7 | 7:43453321 | GACATATATTTTAAA[A/G]GTAGATTTGATGACA | 23072 |
rs73098725 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43460448 | TGGGCTTTTTTAAAG[A/C/G]GGGGAGGTTGTGTAG | 23072 |
rs73098730 | snp | G/T | 0.261056 | 0.249755 | intron-variant | HECW1 | GRCh38.p7 | 7:43462569 | GAATCGGAGACTCAG[G/T]GGGTGGGGCTGGCAG | 23072 |
rs73098732 | snp | A/G | 0.274929 | 0.248754 | intron-variant | HECW1 | GRCh38.p7 | 7:43464350 | ACCTGGGAGTGAAGA[A/G]GTTTTCCAGCATGCC | 23072 |
rs73098739 | snp | A/G | 0.256897 | 0.249905 | intron-variant | HECW1 | GRCh38.p7 | 7:43469340 | CCTAGCCCTCACGCT[A/G]CTAGATGCCAACTGT | 23072 |
rs73098750 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43497609 | TAAGATGGAACAGGG[G/T]CTATGCAGGAGACTA | 23072 |
rs73098755 | snp | C/T | 0.290977 | 0.246619 | intron-variant | HECW1 | GRCh38.p7 | 7:43506302 | AATCACTTCTTGTAG[C/T]AACTTACAAGAAAAG | 23072 |
rs73099556 | snp | C/T | 0.264084 | 0.249603 | intron-variant | HECW1 | GRCh38.p7 | 7:43367206 | GGGAAAGTGACATGG[C/T]ATTTATTTTTTGACT | 23072 |
rs73099566 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | HECW1 | GRCh38.p7 | 7:43371167 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCT | 23072 |
rs73099571 | snp | A/C | 0.0539704 | 0.155153 | intron-variant | HECW1 | GRCh38.p7 | 7:43372352 | TACTAACAAAGGGTT[A/C]TTTTCCTTTTTTTAT | 23072 |
rs73099575 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | HECW1 | GRCh38.p7 | 7:43374213 | ACTACGAAAATTCAT[A/T]GAGGTTGGCTCCTTT | 23072 |
rs73099577 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | HECW1 | GRCh38.p7 | 7:43374886 | AAATTGAAATTCTTC[A/G]TATTTCAGATAGCTG | 23072 |
rs73099580 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376410 | GGGTAGCCAGCCAGC[A/G]TCTGGGCTATGTGGA | 23072 |
rs73099584 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HECW1 | GRCh38.p7 | 7:43378523 | ACCCTTGGCACTTTC[A/G]GCCAGGCATGGTGGC | 23072 |
rs73099593 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43381184 | TTGTCCTCTTTTCCC[A/C]TTGGGCTGTTTACTT | 23072 |
rs73099600 | snp | A/C | 0.0539704 | 0.155153 | intron-variant | HECW1 | GRCh38.p7 | 7:43387149 | AGCCCTCATTCTCCC[A/C]CTCCCTTTCCATCTC | 23072 |
rs73099602 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | HECW1 | GRCh38.p7 | 7:43388879 | GTGCCTCTTGATGAG[A/T]TTGAACCAGGTAAGA | 23072 |
rs73099607 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158617 | TATTCTCCTGCACAA[A/T]CCTTTACAATGAGGG | 23072 |
rs73099611 | snp | A/G | 0.0325976 | 0.123435 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163118 | GCACACAGCACAGAC[A/G]AGAACAGTCCCAAAG | 23072 |
rs73099618 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | HECW1 | GRCh38.p7 | 7:43171574 | ACAGCCTCTTAAAAA[C/T]CATTTCAATACAATA | 23072 |
rs73099645 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43187042 | CTGCCTCAGTCTCTC[A/G]TGAGGTTGCAGTCAA | 23072 |
rs73099664 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | HECW1 | GRCh38.p7 | 7:43200358 | CTTTTAAAATGCTTT[C/T]GTCAAAAACTTAAGA | 23072 |
rs73099673 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43204158 | TTTGCCTTCTTCAAC[A/C]GTAGATGTCAAAGCA | 23072 |
rs73099684 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | HECW1 | GRCh38.p7 | 7:43212572 | GGCCAAGGCTATTAC[A/G]CTGCACTCTTCTTAA | 23072 |
rs73099692 | snp | C/T | 0.302686 | 0.244385 | intron-variant | HECW1 | GRCh38.p7 | 7:43222811 | CTCTTACCATTGGGC[C/T]GTCTCAGGGCTCAGG | 23072 |
rs73099696 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43226216 | GTTCGGAACATCGGG[G/T]TTAAAATGGAAAAAA | 23072 |
rs73100718 | snp | A/G | 0.309401 | 0.24284 | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43512858 | CTCAGGATTGACACG[A/G]TACTCAGCTGTGGCT | 23072 |
rs73100741 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43526360 | GAGCATGAGGGCCTT[A/G]TCTATTATGTTCACT | 23072 |
rs73100742 | snp | A/G | 0.188946 | 0.24243 | intron-variant | HECW1 | GRCh38.p7 | 7:43526905 | GGAGACTAAGGCGAG[A/G]GGATCACTTAACCCA | 23072 |
rs73100744 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43528096 | AGTGAATTGTTCAGT[C/T]GTTTGACCATGAAAG | 23072 |
rs73100750 | snp | A/G | 0.188946 | 0.24243 | intron-variant | HECW1 | GRCh38.p7 | 7:43532417 | TCGGTTCATTCCAAA[A/G]ACCCTACACGAAACT | 23072 |
rs73100755 | snp | C/G | 0.189261 | 0.242509 | intron-variant | HECW1 | GRCh38.p7 | 7:43534622 | AAACAGGGTTCAAAT[C/G]GTATAAGACATTTCA | 23072 |
rs73100756 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43534708 | ATTTTCAGTTTAATT[A/C]CATTCAACAAATCTT | 23072 |
rs73100758 | snp | C/T | 0.188316 | 0.242271 | intron-variant | HECW1 | GRCh38.p7 | 7:43538691 | CTCGGTTTCTTAATC[C/T]GCAAAATGGAGATGA | 23072 |
rs73100769 | snp | A/G | 0.186105 | 0.241697 | intron-variant | HECW1 | GRCh38.p7 | 7:43550858 | GCATGTGACCCTGGC[A/G]TGCCAGACGTGAAAA | 23072 |
rs73100771 | snp | C/T | 0.187685 | 0.242109 | intron-variant | HECW1 | GRCh38.p7 | 7:43551666 | TAGGAGTGGAGCATG[C/T]GATTCTTTTTTCTGT | 23072 |
rs73100779 | snp | C/T | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43553873 | CACAAGCCCTTTGCA[C/T]GCTGCTCGTAGCTTC | 23072 |
rs73100784 | snp | C/G | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43558428 | GGAGTTGGAGGCCTG[C/G]TTAAGTTAGTAGTTG | 23072 |
rs73101109 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43233750 | TCCTCAGTAGCTCCA[A/G]GCCTGCACCAGTCAG | 23072 |
rs73101125 | snp | A/G | 0.408017 | 0.193729 | intron-variant | HECW1 | GRCh38.p7 | 7:43246285 | TCCAGCCTGCGTGAC[A/G]TAGCAAGACCTTGTC | 23072 |
rs73101126 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43247013 | GAGTGGAAGGAGTTG[A/G]TGGCTGGAAGCTGTC | 23072 |
rs73101135 | snp | A/G | 0.122758 | 0.215196 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248229 | GAGGTGGAGCCCCAG[A/G]GCTCCTGACAGCAAC | 23072 |
rs73101143 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | HECW1 | GRCh38.p7 | 7:43251063 | CAGGGACCCCACCCC[C/G]CTTACTGGATGGGCC | 23072 |
rs73101148 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43252112 | CACTATCAGAACCAT[A/G]CACCTGCGAGCCCTC | 23072 |
rs73101153 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HECW1 | GRCh38.p7 | 7:43253039 | AAGTCTGTCTGCTCA[A/G]TAAAATCATCTGTGG | 23072 |
rs73101154 | snp | C/T | 0.261884 | 0.249717 | intron-variant | HECW1 | GRCh38.p7 | 7:43253123 | CAAGGCTCAAACATC[C/T]GCACTTTAAAAAAAA | 23072 |
rs73101174 | snp | C/T | 0.262435 | 0.249691 | intron-variant | HECW1 | GRCh38.p7 | 7:43255986 | GACCTAATTATTTAA[C/T]ATGAAGAGGTATGAA | 23072 |
rs73101304 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | HECW1 | GRCh38.p7 | 7:43393933 | CATACTCTAGACTTA[C/T]GATTCTATAAACTAT | 23072 |
rs73101306 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | HECW1 | GRCh38.p7 | 7:43394228 | AGGACTGGCCACCTT[C/T]AGAGTTAAGAAAAGC | 23072 |
rs73101368 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | HECW1 | GRCh38.p7 | 7:43395397 | CCCTTTCACTGTCTC[A/G]GCCATAATTTTGCAA | 23072 |
rs73101370 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | HECW1 | GRCh38.p7 | 7:43396708 | AATCACTGTCTTCGT[A/T]GCCTGTAGCTGGTAA | 23072 |
rs73101371 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | HECW1 | GRCh38.p7 | 7:43396716 | TCTTCGTTGCCTGTA[A/G]CTGGTAAAATCACTG | 23072 |
rs73101376 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | HECW1 | GRCh38.p7 | 7:43398786 | CAAATCAGTCTCCCC[A/G]AGAATTCGGCCATCA | 23072 |
rs73101377 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43401975 | AAGAGAAGGAGCATC[A/C]GAATGTTGAGAGGAG | 23072 |
rs73101386 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43405730 | GCACAGTGAGCCACT[C/T]GTACCCGTTCTGGGA | 23072 |
rs73101387 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43405731 | CACAGTGAGCCACTC[A/G]TACCCGTTCTGGGAA | 23072 |
rs73101390 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | HECW1 | GRCh38.p7 | 7:43406454 | TTAAATAAGTGCATA[C/T]GAAAACAACTGTGCT | 23072 |
rs73103320 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43435626 | AGCTATGTTTGGAAG[C/T]GAACACTTATTTACA | 23072 |
rs73109083 | snp | A/G | 0.187053 | 0.241946 | intron-variant | HECW1 | GRCh38.p7 | 7:43280734 | TGTTGGAAAGAGAAC[A/G]AACACACAAAGGACC | 23072 |
rs73111014 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | HECW1 | GRCh38.p7 | 7:43290304 | GTTATACCACAGTCA[A/G]TTTGGAAAGTAAGCC | 23072 |
rs73111028 | snp | C/G | 0.102726 | 0.202016 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298832 | CAGGCTCTGTCTGCC[C/G]CCCCCACATCTCGAG | 23072 |
rs73111030 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299273 | TGAGCAAAGATTCCA[C/T]GAGGCCGGAATCGGT | 23072 |
rs73312808 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118313 | TGACATCCATTTAAC[A/G]TGCATGGATGTTCCC | 23072 |
rs73312814 | snp | A/C | 0.0599851 | 0.162463 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119041 | ATATTTGATTTTGAC[A/C]AACAGCACATTGAAC | 23072 |
rs73312816 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120288 | ACCTGCATCCTGACC[A/C]CCTTTATCAGATATC | 23072 |
rs73312819 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122543 | TAGCAAACTTTTTGA[G/T]GAGACCTCTCTCATA | 23072 |
rs73312825 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126197 | CCTTCCCTTTTATAA[C/T]TGTTCTATTTTCTCT | 23072 |
rs73312899 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155368 | AACTGGAAGTTGGAG[A/G]GGAAAAAAGGAGACT | 23072 |
rs73314706 | snp | A/G | 0.117537 | 0.212022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158901 | AGGTTCTCAAACTAT[A/G]CTGTGCATCAGAATC | 23072 |
rs73314711 | snp | C/T | 0.173965 | 0.238157 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159642 | ATTTCCTTATATCTT[C/T]ACAAATATATGAAAG | 23072 |
rs73314720 | snp | A/G | 0.17654 | 0.238964 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162618 | GCCAGGCATTAGGAC[A/G]TGGACATATCTTTTG | 23072 |
rs73314730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43167994 | CATACCCCTCACCAA[C/T]ACCACACCACCAAGT | 23072 |
rs73314731 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43168275 | GTGTGAGAGACAGAG[A/T]GAGAGAGACAAGGAA | 23072 |
rs73314734 | snp | A/G | 0.110519 | 0.207473 | intron-variant | HECW1 | GRCh38.p7 | 7:43168308 | ATACAGCTATTATAC[A/G]GTATGTGGTGTGCAG | 23072 |
rs73314738 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | HECW1 | GRCh38.p7 | 7:43169890 | GAGACAATCCCCTAC[C/T]TGGTGAGGCTGATTG | 23072 |
rs73314741 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43170069 | TGGCCTGTTGGGAAC[C/T]GGGCCTCACAGCAGG | 23072 |
rs73314742 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43170360 | AAAATCATCCTCCCC[A/C/T]ACCCCTGTCTGTGGA | 23072 |
rs73314756 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43186392 | TGATACCATGGCTGG[A/G]CGCAGTGGCTCACGG | 23072 |
rs73314763 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | HECW1 | GRCh38.p7 | 7:43195775 | AGAGAGTTTGCCCCA[C/T]GGATTTGGGCTGCTA | 23072 |
rs73314775 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | HECW1 | GRCh38.p7 | 7:43208829 | TGTCTGGCTTCCAGC[A/G]TGGAACCGGAGGTCT | 23072 |
rs73314776 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43208837 | TTCCAGCATGGAACC[A/G]GAGGTCTGGATTCAT | 23072 |
rs73314781 | snp | A/G | 0.0425829 | 0.139564 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214138 | CACATATGTATTTCT[A/G]TAGTTTTTCTAGTTT | 23072 |
rs73318417 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43230000 | CATCGTGGCTTCTGT[A/G]GCTCCTGCTGAAGTC | 23072 |
rs73318425 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43239339 | CTGAGCTTACTTTGT[C/G]TTTGCAAGGGTGTCT | 23072 |
rs73318428 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43239801 | CCACTCCAGGGCTTC[G/T]TAGCTGTGATGCGCT | 23072 |
rs73318431 | snp | A/G | 0.263809 | 0.249618 | intron-variant | HECW1 | GRCh38.p7 | 7:43240871 | CCGCCCTGCTCTCCT[A/G]TTGCTGTGCCACAAG | 23072 |
rs73318433 | snp | C/T | 0.189261 | 0.242509 | intron-variant | HECW1 | GRCh38.p7 | 7:43240910 | GAGGGACCCTCCCCA[C/T]GTGACTTCCTGCTGC | 23072 |
rs73318463 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43250570 | GGACAGGGGAAGGAA[A/G]GTGGAGAAGAGAGCG | 23072 |
rs73318477 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | HECW1 | GRCh38.p7 | 7:43256782 | TATTTCCTAGAACAG[A/G]ACCTGCTATTCTTCA | 23072 |
rs73318478 | snp | C/T | 0.079617 | 0.182947 | intron-variant | HECW1 | GRCh38.p7 | 7:43256828 | TCTGGCTTCCCCTCC[C/T]CCAACAACCTCCCTC | 23072 |
rs73318480 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | HECW1 | GRCh38.p7 | 7:43256862 | AAAAAGAAAGAAAGT[A/G]AGGTATATAAACCAT | 23072 |
rs73318492 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | HECW1 | GRCh38.p7 | 7:43264089 | ACATAGTTATTTTTT[A/G]TGGTGAGAACATTTA | 23072 |
rs73318495 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43264138 | GTTTTGAAATATGCA[A/G]CACCTTATTATTAAC | 23072 |
rs73320408 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43271458 | CTGTACTTAGAAAAC[C/G]CTAAGGACTCTGTCA | 23072 |
rs73320443 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43289994 | AGGATAAAGCGGGTT[A/G]TGGAGGCCAAGGCCT | 23072 |
rs73322335 | snp | C/T | 0.029116 | 0.117091 | intron-variant | HECW1 | GRCh38.p7 | 7:43313836 | TAGACTGGCCTGTAA[C/T]CTTCAGTGTTGCCAC | 23072 |
rs73322347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43316738 | GCTTGGCCCACAGCA[A/T]CCATTCCAGTTCTCC | 23072 |
rs73322357 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43322987 | AAATATTAAGGAAGA[C/G]GAAATCCTAGGTGGG | 23072 |
rs73322386 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43341733 | TAATATAACCAGTCC[A/G]TAATACAGCATTCTA | 23072 |
rs73322388 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43343192 | AGATATTGTAACACC[A/T]GAGTAGCTAAAAACT | 23072 |
rs73326123 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43353702 | TGATTTATACACTGG[A/G]AAAAGTGAAATGGAG | 23072 |
rs73326124 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43353966 | ATAGATCCCCTTGGC[A/G]TGAGCCCTTAGCCAG | 23072 |
rs73326128 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43355720 | CCAGAGGCCAGGCAC[A/C]GTAGCTCATGCCTGA | 23072 |
rs73326132 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | HECW1 | GRCh38.p7 | 7:43357114 | AAAAAGGGGAGCCCT[C/T]ATACACTGCTGGTGG | 23072 |
rs73326143 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43361618 | GTGGTAATAGATGCC[A/G]TCTTCCTAAGTTACA | 23072 |
rs73326146 | snp | A/G | 0.208779 | 0.246578 | intron-variant | HECW1 | GRCh38.p7 | 7:43362812 | ACCCTTCCACTGCAG[A/G]CCTGGCCTCTTGCCA | 23072 |
rs73326152 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43364228 | AATTTTCTGAGCATT[G/T]TATGGTCTCACGATG | 23072 |
rs73326157 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43365202 | GGAGACTCTGATGCA[A/G]TCTGAAGCTGTTGGT | 23072 |
rs73326161 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43369680 | GACATGAATATATCC[A/G]GTGACCTAGAAAAAA | 23072 |
rs73328022 | snp | A/T | 0.0748431 | 0.178382 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377180 | GGAGGAAGGCAGCCC[A/T]GGCCCATCTCCTCCT | 23072 |
rs73328024 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43379351 | CTGCACACACACTCC[C/T]ATGCTGTGCCTCCTT | 23072 |
rs73328033 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43387505 | AGAGAAACAGGACCA[C/T]CCATCTTCAGGTCTT | 23072 |
rs73328038 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43390771 | GCCAGGTCTCACTAA[C/T]ACAGGCCTCCGTTAC | 23072 |
rs73328040 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43391326 | TTATAGAAATGAAAA[C/G]TCTCTTCCTCCCCAG | 23072 |
rs73328051 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | HECW1 | GRCh38.p7 | 7:43398389 | TTAAGGGGACACAGC[A/G]GCATAAAGCCTGAGG | 23072 |
rs73328054 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | HECW1 | GRCh38.p7 | 7:43404256 | TAAGTCTTTATAAAG[A/G]AAAGTGTAAACATTT | 23072 |
rs73328064 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43408260 | GTTTATCCTATCTTC[A/T]TGATTTGCAAAGGGC | 23072 |
rs73328068 | snp | C/T | 0.030665 | 0.119967 | intron-variant | HECW1 | GRCh38.p7 | 7:43410265 | CCCAGGATGCTGGCA[C/T]GGTTGGGTTCTGGTG | 23072 |
rs73328083 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | HECW1 | GRCh38.p7 | 7:43423751 | TTTAGTGAAATCAGC[C/T]ATCGAGGGAGTATTT | 23072 |
rs73328092 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | HECW1 | GRCh38.p7 | 7:43432447 | CCCGGCCCAGTTGTT[A/T]ATTTTTTAAGACTCA | 23072 |
rs73328095 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | HECW1 | GRCh38.p7 | 7:43432647 | AGCTGTGTCCCAGCA[C/T]CCAGCTCACAGCCAG | 23072 |
rs73328100 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43442023 | TTTTCCTTGGCTAGC[A/G]ATACACAACACGATA | 23072 |
rs73328102 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | HECW1 | GRCh38.p7 | 7:43442451 | GCCTGCCTCACCCAC[G/T]GGTATAGAAAGCACA | 23072 |
rs73329806 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43450704 | CAAACTGACACACAC[A/G]CACAAATGGATTTCC | 23072 |
rs73329807 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43453926 | TCTTTACAAAGCAAC[A/C]CAGAAAACATGTTCA | 23072 |
rs73329814 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43470696 | TTTCAAATGAGAAGA[C/T]TTTCAGTTATGACAC | 23072 |
rs73329819 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43479165 | TAATGAAATAATCCT[A/T]TAGCTCACTGTGATG | 23072 |
rs73329821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43484618 | GTTTCTATATTAAGG[A/G]TCCTAAATGGTAAAA | 23072 |
rs73329838 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43512999 | AGTTCCCTCTAAAAA[A/T]TAAGCTCTATTGGAG | 23072 |
rs73329844 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521130 | CTGATGTGGTTTGAC[A/G]GATGCGTCTCTCAGA | 23072 |
rs73329845 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521933 | GATTAAGTCATGAGG[G/T]CTCCACCTTTGTGAA | 23072 |
rs73329848 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43549240 | GTCTTTAACTGGGCC[A/G]CTAAAAATCAGACAT | 23072 |
rs73329850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43556991 | GACCTCTTCTTGGGA[C/T]AAGAAGCAAATGCCT | 23072 |
rs73689973 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43292703 | CAGCACATGTCACCC[A/G]GCACCCGGGGCTCTT | 23072 |
rs73689976 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HECW1 | GRCh38.p7 | 7:43311076 | AAACAATACAAAAAT[A/G]CATTTTTTCTCATCA | 23072 |
rs73689977 | snp | G/T | 0.00686306 | 0.0581759 | missense | HECW1 | GRCh38.p7 | 7:43311811 | GCCATGGCGTCTCCT[G/T]CTAGAAACTCCCAGA | 23072 |
rs73689980 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43325160 | TTTTTCTCCAGTGGG[A/C]ACCTGGCTATTTGAC | 23072 |
rs73689984 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43327019 | GCATGTTTTCACCAG[A/G]ACTGCTCTGCCTTTA | 23072 |
rs73689985 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43328986 | AGGGGCTCAGATCTA[A/G]ACATGCAGGCTCCGT | 23072 |
rs73689992 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43366557 | GTTGCCGACTGATGG[C/G]ACCAGCTACCTAGAA | 23072 |
rs73689993 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43368352 | CCACAGCCATGATTT[C/T]TGATCAAGCCTTTTA | 23072 |
rs73689999 | snp | C/T | 0.491936 | 0.0629843 | intron-variant | HECW1 | GRCh38.p7 | 7:43401587 | TTTTTTTTTTTTTTT[C/T]CCCCAAATATAGCCA | 23072 |
rs73690251 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111020 | ACATCAATAACCTCT[A/G]TGAGAGATGTGGACT | 23072 |
rs73690252 | snp | A/G | 0.00485984 | 0.0490541 | intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114371 | CTCATCAGCAGACTC[A/G]CTCCGGCTGTGGCTA | 23072 |
rs73690253 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117265 | ACAGCTGAATAACTC[C/T]TATGGTCAAAGTGTT | 23072 |
rs73690254 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119643 | GCATCTCCCTTTGAA[C/T]GGCACGTTAGCTTAA | 23072 |
rs73690255 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121297 | AACTGTTCTTTGCTT[C/T]CTCTGGGCCACACTG | 23072 |
rs73690256 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123945 | ATGAACCATTTAAGC[C/T]ATATAGAGAAAGTTG | 23072 |
rs73690257 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135311 | GGAGATGACTCATCT[A/G]ACATGCCTCATTCAC | 23072 |
rs73690258 | snp | G/T | 0.115438 | 0.210697 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139075 | GTGCCATTTTAATTG[G/T]TGTTCTTTTTGTTTC | 23072 |
rs73690259 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148534 | CCCTGCCCTTTACAT[A/G]TGCAGAAACTCAGGT | 23072 |
rs73690261 | snp | A/G | 0.0603597 | 0.1629 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163031 | AAATCCTGTGTGACT[A/G]TGAAACTCATTAACT | 23072 |
rs73690262 | snp | A/G | 0.208169 | 0.246476 | intron-variant | HECW1 | GRCh38.p7 | 7:43163995 | CAGGAGGTGGGCAGG[A/G]GTTCATCCTGCCCTG | 23072 |
rs73690264 | snp | A/T | 0.110872 | 0.20771 | intron-variant | HECW1 | GRCh38.p7 | 7:43168319 | ATACAGTATGTGGTG[A/T]GCAGGGATACAGGTG | 23072 |
rs73690265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43176568 | TTCACACAGTGGGGG[A/G]CTCACAATAGATGGT | 23072 |
rs73690266 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | HECW1 | GRCh38.p7 | 7:43183160 | ATAGTCTTTTGTGTA[C/G]GTACACATCTACCAT | 23072 |
rs73690267 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | HECW1 | GRCh38.p7 | 7:43205361 | CAAACAATAAATTCT[G/T]TCGGCAGCATTGAGT | 23072 |
rs73690268 | snp | C/G | 0.145636 | 0.231217 | intron-variant | HECW1 | GRCh38.p7 | 7:43206275 | GCAGCTGATCTGCCA[C/G]GGAGTCAAGAGGATC | 23072 |
rs73690269 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | HECW1 | GRCh38.p7 | 7:43206589 | CTGAAGCTCATTAAT[C/G]TCTGTATTGTACTCT | 23072 |
rs73690270 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43215239 | CCTGGAGAGCCCTTG[C/T]TGTGCCCGCATTAAC | 23072 |
rs73690271 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43222258 | ATTCAGAGAACCTGG[G/T]TTTTTTTTGCTCTGA | 23072 |
rs73690272 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | HECW1 | GRCh38.p7 | 7:43226908 | CACAGGATGGGGGCC[A/G]TCTCCAGCCGTCCAA | 23072 |
rs73690273 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | HECW1 | GRCh38.p7 | 7:43227885 | TCTGATACATGATAA[A/G]GGGGAAGCAGGTTAC | 23072 |
rs73690274 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | HECW1 | GRCh38.p7 | 7:43228786 | CTAAATGGTAGTATG[C/T]TTATAAAAGGCATCC | 23072 |
rs73690275 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | HECW1 | GRCh38.p7 | 7:43228881 | AATTGCGTATACAAT[A/G]TGTCTTAAGACAAAA | 23072 |
rs73690276 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | HECW1 | GRCh38.p7 | 7:43233503 | AAAAGGTGGTGGTGC[A/G]GTCCATTTAGCAGGC | 23072 |
rs73690277 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | HECW1 | GRCh38.p7 | 7:43233523 | ATTTAGCAGGCCGAT[A/G]ATAGATTTTCCTGGA | 23072 |
rs73690278 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | HECW1 | GRCh38.p7 | 7:43233599 | TGAAAGCTTCCAAAA[C/T]GGTGCAAAATAATAC | 23072 |
rs73690279 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | HECW1 | GRCh38.p7 | 7:43233941 | GAAATAGATTGCAGC[C/T]TCTGGTACGGGAAAG | 23072 |
rs73690280 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | HECW1 | GRCh38.p7 | 7:43234859 | TTTGCTGAGTGAATG[C/T]ATGAATGAAAAGCCC | 23072 |
rs73690281 | snp | A/G | 0.078151 | 0.181571 | intron-variant | HECW1 | GRCh38.p7 | 7:43235499 | ATTTTGAACTCAAGA[A/G]AAAGAAAACATGGAC | 23072 |
rs73693014 | snp | C/T | 0.115788 | 0.21092 | intron-variant | HECW1 | GRCh38.p7 | 7:43529156 | AAAACTCTAAAATCC[C/T]ACTGTCAATCATTCT | 23072 |
rs73693015 | snp | C/G/T | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43530910 | ATTTCTCTAAAAATG[C/G/T]CAAAACAAGCATGTC | 23072 |
rs73693017 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43531024 | CAGGACCTCCTGCTA[G/T]CTCTCTCCACAACCT | 23072 |
rs73693019 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | HECW1 | GRCh38.p7 | 7:43540296 | ATAAGGTGAAAACCT[A/G]CTTAGAGTGGACACC | 23072 |
rs73693020 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | HECW1 | GRCh38.p7 | 7:43540957 | TGGCTGGAAGAGGAG[C/G]CTTCCTTTAGTCCCT | 23072 |
rs73693022 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | HECW1 | GRCh38.p7 | 7:43549076 | GCATCCCAACCATCA[A/C]AACTGTGTTCAGTGC | 23072 |
rs73693023 | snp | A/G | 0.031825 | 0.122064 | intron-variant | HECW1 | GRCh38.p7 | 7:43549374 | GACTACTTATGGACT[A/G]CTTTGTTTAGGTACC | 23072 |
rs73693026 | snp | C/T | 0.046775 | 0.145601 | intron-variant | HECW1 | GRCh38.p7 | 7:43555487 | CGCTATAGTGAGAAA[C/T]GCTGCTGCAACAGAC | 23072 |
rs73693028 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | HECW1 | GRCh38.p7 | 7:43555951 | TTGGAAACATCTTGC[C/T]TTTATTTTAGAGAAA | 23072 |
rs73693030 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43558371 | GAAATTCTAATATGA[A/G]CATGTTTCACTGCAG | 23072 |
rs73693031 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | HECW1 | GRCh38.p7 | 7:43558635 | ACAGCTCCCACAACA[A/G]AGAGTTATCAAGTTT | 23072 |
rs73693032 | snp | A/G | 0.031825 | 0.122064 | intron-variant | HECW1 | GRCh38.p7 | 7:43561002 | GTTTCTGTAAAAACA[A/G]AGAACTTCTGGCAGG | 23072 |
rs74323979 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43422783 | TGAGTAAATGAGAAT[A/G]AGACTTATTAGAAAG | 23072 |
rs74325076 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43474669 | AGTTTGACAGATTAA[A/G]TAGACAAAATAATTT | 23072 |
rs74328229 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43166981 | GCAGCCACTGAATGA[C/T]GCAAGGCAGGCAAGA | 23072 |
rs74330012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43235692 | CCCACTAACAAGATA[C/T]GTGAATCTTTATGTT | 23072 |
rs74333247 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147823 | TTGGGTTAATTGCAC[C/T]GTCTAGTTTATTTTC | 23072 |
rs74339799 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | HECW1 | GRCh38.p7 | 7:43229169 | CCGGTGTTGAGCTCT[C/T]TCCTCCTTCCCTATG | 23072 |
rs74344933 | snp | A/G | 0.107341 | 0.205301 | intron-variant | HECW1 | GRCh38.p7 | 7:43262528 | TGATTTTAAAACTAT[A/G]TTCTTTCCCTGGTGT | 23072 |
rs74355700 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | HECW1 | GRCh38.p7 | 7:43292572 | TAAGCACAAGTGTGG[C/T]CCAGAGCCTGAGAGG | 23072 |
rs74357958 | snp | C/T | 0.190519 | 0.242821 | intron-variant | HECW1 | GRCh38.p7 | 7:43398793 | GTCTCCCCGAGAATT[C/T]GGCCATCAGAATTTT | 23072 |
rs74365405 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43560286 | TCTAGGTAAAGTATT[C/T]CAATTATTTTCTTTT | 23072 |
rs74366553 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | HECW1 | GRCh38.p7 | 7:43168141 | GAGAGGGACTGGACA[C/T]GTTTCACTTTTGCAT | 23072 |
rs74368380 | snp | C/T | 0.308661 | 0.24302 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509233 | AGTGGCCAGATGTTA[C/T]GAGGGATGAGAGTGA | 23072 |
rs74377098 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | HECW1 | GRCh38.p7 | 7:43531847 | CATCTTCCAGATCCC[C/T]GAATGCTGCATCAAT | 23072 |
rs74388191 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43530695 | AATACCTACTAGACA[A/T]CTCCACTTTGATCCT | 23072 |
rs74395640 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43496863 | TCAAGGGGCATGGAG[A/G]TGGTCCTTCAACTAG | 23072 |
rs74396683 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144099 | TAGACACCTGTTGGC[C/T]GTAAGAGTTTCTCGG | 23072 |
rs74399349 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43419293 | CCACTGTGAAGAATT[A/C]ATTCCATGCCCGTCT | 23072 |
rs74404930 | snp | G/T | 0.113334 | 0.209338 | intron-variant | HECW1 | GRCh38.p7 | 7:43505323 | CCTCTTAAATACATC[G/T]CCTCTCTGCCCACTT | 23072 |
rs74415903 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43435614 | CTAGTTCTGAGGAGC[C/T]ATGTTTGGAAGTGAA | 23072 |
rs74431384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43164623 | CCTGCAGGGCCAGCA[G/T]CCATGGCACAGTCCT | 23072 |
rs74441370 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HECW1 | GRCh38.p7 | 7:43433437 | GGGACCCAGTAATGG[A/G]TACTATTGTGGAAGC | 23072 |
rs74449390 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43471144 | ATGTCCCCAAAAATA[A/G]TCCAAGATCAAGATT | 23072 |
rs74485317 | snp | C/G | 0.0839998 | 0.186933 | intron-variant | HECW1 | GRCh38.p7 | 7:43389306 | CTGCTGGAGCCGTCC[C/G]CAGACTTACAAAATC | 23072 |
rs74499953 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43316409 | GAGGGCCCTATTTTT[G/T]GCCCAGATTCTAAGC | 23072 |
rs74553293 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43323887 | AAAAACACAAAAATT[A/G]GCTGGGCTTGGTGGC | 23072 |
rs74557687 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43333314 | AGTGGGGAGCTCAGT[C/G]TGCCTCCTATAAAAA | 23072 |
rs74615165 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43321225 | GGCCACAGCTCCCCC[A/G]GAGGGCTGTGAGACA | 23072 |
rs74617482 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43372721 | TTAAATTTTTTTTAA[A/T]TATTCCCTTTTCTCT | 23072 |
rs74624403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43461425 | TACAGTTCTGGAAGA[A/G]CATGTGGGTCTAAAA | 23072 |
rs74639630 | snp | A/G | 0.166832 | 0.235761 | intron-variant | HECW1 | GRCh38.p7 | 7:43401356 | TCCAAAAAGGACGAG[A/G]GAAAAAAAGATGAAT | 23072 |
rs74653003 | snp | G/T | 0.175576 | 0.238665 | intron-variant | HECW1 | GRCh38.p7 | 7:43240040 | AATTAGGAAAAAAAG[G/T]TTTTTTTAAATGTCA | 23072 |
rs74653984 | snp | A/C/T | 0.0776269 | 0.181906 | intron-variant | HECW1 | GRCh38.p7 | 7:43332708 | ATGGGCTGCAAGGTC[A/C/T]GACCCCTGGGCTGTT | 23072 |
rs74659208 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426977 | ATATCTCTACTATCT[C/G]TTTTTATTAATCTGA | 23072 |
rs74659318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43367597 | AAAAGTAATCTTGAG[G/T]GCTTGAGCTAGAATT | 23072 |
rs74671995 | snp | G/T | 0.177182 | 0.23916 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298175 | TGCACCATTCGCCCT[G/T]TCTGGAATATTCACC | 23072 |
rs74703512 | snp | A/G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43342843 | ATCCTGGCTAACACA[A/G/T]GGAAACCCTGTCTCT | 23072 |
rs74709776 | snp | A/G | 0.040671 | 0.13668 | intron-variant | HECW1 | GRCh38.p7 | 7:43224165 | TGTCATCTAGAAAAG[A/G]CACATAAAATGAATG | 23072 |
rs74712844 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | HECW1 | GRCh38.p7 | 7:43323755 | TGGCTTGACCGTGCG[C/T]GGTGACTCATGCCTA | 23072 |
rs74723586 | snp | G/T | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43273819 | TGGATAATTTCCCAT[G/T]TTCCCTTAATATATG | 23072 |
rs74735666 | snp | A/G | 0.177503 | 0.239258 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162699 | GGAGAAAAACTGAGT[A/G]AGATCTCACTTGGAG | 23072 |
rs74738367 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160178 | TTTGCCCATTTTTCT[A/G]TGGGTCTGTTTGTCA | 23072 |
rs74743192 | snp | A/G | 0.186421 | 0.24178 | intron-variant | HECW1 | GRCh38.p7 | 7:43551437 | ATGGAAAATACAGTC[A/G]TTTTAATACAAATGC | 23072 |
rs74748966 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | HECW1 | GRCh38.p7 | 7:43218127 | GCTTTAGAAACAGGA[C/T]TTTGCAGGTGAAAAC | 23072 |
rs74754346 | snp | C/T | 0.201418 | 0.245234 | intron-variant | HECW1 | GRCh38.p7 | 7:43407985 | TCAGAACCCATGCCG[C/T]GAGCAGGACGGCCTT | 23072 |
rs74764443 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43534657 | TTTTCTGTGGGTTTG[G/T]ATAGTTGCGCTCCAC | 23072 |
rs74779735 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43253911 | GAAATTCCGTCTCAG[A/G]AAAAAAAAAAGACAG | 23072 |
rs74783680 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43202246 | CACAATGCACACTGT[C/T]CTCTCCCAACAGTTT | 23072 |
rs74792109 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43474970 | AGAGGTTCCCAGGGG[C/T]TTCAAGGAGTAGAAA | 23072 |
rs74792376 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | HECW1 | GRCh38.p7 | 7:43554865 | TATTTGATTTTGAGT[A/G]ACCATCCTTTGGGAT | 23072 |
rs74818441 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | HECW1 | GRCh38.p7 | 7:43358204 | AGAGTAACTCATGCA[C/T]TAGGCAACACTAACT | 23072 |
rs74829566 | snp | A/G | 0.188631 | 0.242351 | intron-variant | HECW1 | GRCh38.p7 | 7:43468405 | TGGCTGAGACAGCGA[A/G]AAAACCATGTGGAGT | 23072 |
rs74831767 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43314430 | CAGTGAGAGGGGGCA[A/G]GGGAGAGGCAGACGA | 23072 |
rs74845161 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43338927 | TCACTATTTCACCTA[C/T]AGTTTTGAAGAGTAA | 23072 |
rs74848841 | snp | C/T | 0.120326 | 0.21374 | intron-variant | HECW1 | GRCh38.p7 | 7:43488747 | TTGGAGAAGGGCGTT[C/T]CCATCCAATCCTCCT | 23072 |
rs74859064 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43370886 | TTTAGGGCAATGATA[A/T]TCTTTTTTTTTTTTT | 23072 |
rs74866578 | snp | A/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149004 | TTCCAATTGATAAAC[A/G]TAGAAGAAATTAAGG | 23072 |
rs74873247 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43366669 | TAAATGGCAAGACCA[A/G]GTTCCAATAAACATC | 23072 |
rs74878644 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43291118 | ACAGAATGCTTGTTC[C/T]GTGGTGCTGCAAAGA | 23072 |
rs74880245 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297257 | ATACAGTCAGAGCAA[A/G]GGCACATTTCAGTCC | 23072 |
rs74881291 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43242888 | CGTCCACCAGGGCGT[G/T]GGACACAGAGCAGGA | 23072 |
rs74900446 | snp | C/T | 0.218151 | 0.247963 | intron-variant | HECW1 | GRCh38.p7 | 7:43194036 | ATGTTTGGAATTTGG[C/T]ATCTTATTGTTGCAA | 23072 |
rs74904823 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43265478 | TCAGATAACATAAGT[C/T]TATGTTGAAATGTAT | 23072 |
rs74906678 | in-del | -/G | 0.0535932 | 0.154675 | intron-variant | HECW1 | GRCh38.p7 | 7:43271789 | ACAAAGCAATCCACA[-/G]ATACAACACTATTCT | 23072 |
rs74909984 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43505226 | TTTCTACTCCTCCCC[A/G]TCTCAGTGAATGTCA | 23072 |
rs74914304 | snp | A/C | 0.0737376 | 0.17729 | intron-variant | HECW1 | GRCh38.p7 | 7:43234055 | AGTCTGCAAGAGCAG[A/C]GTGCAATATACGGGT | 23072 |
rs74915008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43176329 | CTTCAATAAGAGGTC[A/G]TGAAGCAGTCCTCAT | 23072 |
rs74919091 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43406055 | AAGAACATGTCAACC[C/T]TGATGTTATGACAGA | 23072 |
rs74933869 | snp | A/G | 0.046775 | 0.145601 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128552 | CACCCAAGAGCACTG[A/G]TGAAGATATACAAGG | 23072 |
rs74963759 | snp | C/G | 0.0322737 | 0.123236 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520823 | TGTGCAAAATAGCTT[C/G]AGAAAGCACTGCTCT | 23072 |
rs74963922 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43223620 | GCAAAACTCCGTCTC[A/C]AAAAAAAAAAAATAT | 23072 |
rs74968148 | snp | A/G | 0.257732 | 0.24988 | intron-variant | HECW1 | GRCh38.p7 | 7:43433509 | AAAGCAAAAGTAAGC[A/G]TCCCAACATCTGCGC | 23072 |
rs74970364 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43465641 | GCAGCGAAGTCCCAA[A/T]ACAACTGGGTGTGGA | 23072 |
rs74974494 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133065 | ATTTACTGAAGTTAA[A/C]TAGTGCGTTTTTTCC | 23072 |
rs74992534 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43307192 | TTTTTTCAAGCGTCA[A/G]CTAAAATCTATGCTT | 23072 |
rs75005191 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | HECW1 | GRCh38.p7 | 7:43498870 | AAAAGGTCAAATTGA[C/T]TATATTTTTTGCCTG | 23072 |
rs75030873 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43202324 | ATCAAAAAATTGTGT[A/G]TGCATATTTTTGGGC | 23072 |
rs75053289 | snp | G/T | 0.195214 | 0.243923 | intron-variant | HECW1 | GRCh38.p7 | 7:43406541 | CCCTGATCCTGTGTA[G/T]CTTTACCTCCATTTG | 23072 |
rs75066406 | snp | A/G | 0.263809 | 0.249618 | intron-variant | HECW1 | GRCh38.p7 | 7:43364928 | TAAGCCCCATGATAT[A/G]TTTTTCTTTCTCTGA | 23072 |
rs75076101 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43283124 | AGTAAGACTATCTCC[A/C]AAAAAAAAAAGAAAG | 23072 |
rs75085341 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43533893 | TGATGCATCAAAAGA[C/T]GCAGAAGCCAAGAAT | 23072 |
rs75100459 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124468 | ATAAGGAACCTAAGC[C/G]ATGGTCCCATTCAAC | 23072 |
rs75117792 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43171429 | AAAGCTTGAATGAAC[A/G]TTGAAAAGTTTGGGC | 23072 |
rs75134620 | snp | A/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514745 | TAAGCTAAATAATGA[A/T]GGATCCATTGAGAAC | 23072 |
rs75148026 | snp | A/G | 0.182296 | 0.240658 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295643 | GGGAGGAGTGGTGGA[A/G]GAGGGGCTGGTGGCG | 23072 |
rs75150328 | snp | A/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134465 | CTTCCCACCTATAGA[A/T]TTTTGGGAAAGTCTA | 23072 |
rs75150415 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | HECW1 | GRCh38.p7 | 7:43435487 | AATCAGACGTACCAC[A/G]TGGTCACTGTGGAAC | 23072 |
rs75151919 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43242468 | CAGGGAGCTCTAAGC[A/G]GCAGAGGAACCATGA | 23072 |
rs75157487 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546095 | CTTCTTCCCCTTCTG[A/C]ACCTGGCACTGGTTC | 23072 |
rs75166474 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43199808 | AGTACCCACGAATGA[A/G]TGCTATTTCCTGTTA | 23072 |
rs75168393 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | HECW1 | GRCh38.p7 | 7:43353660 | TCTACCTGGCACCAA[C/G]TGCATGGAAAATTTT | 23072 |
rs75187326 | snp | A/G | 0.143622 | 0.226238 | intron-variant | HECW1 | GRCh38.p7 | 7:43371752 | ATGATACACTCTAAC[A/G]GCAAAAGCAGCAGGG | 23072 |
rs75197290 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43271062 | GTTTAATGCAAATCT[A/C]AAAATGTCAAGGAGA | 23072 |
rs75198465 | snp | A/T | 0.0655868 | 0.168795 | intron-variant | HECW1 | GRCh38.p7 | 7:43241237 | GGAGTAGAAGCACTC[A/T]TCAGATGGCTTTTGT | 23072 |
rs75212656 | snp | A/G | 0.190519 | 0.242821 | intron-variant | HECW1 | GRCh38.p7 | 7:43379183 | TAATCTTATGACCAC[A/G]GATCTCAAGCTCCCT | 23072 |
rs75222906 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43500440 | TTACCCAGCTCCACT[C/T]CTGACTGTCTTAGCT | 23072 |
rs75229861 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43367619 | GCTAGAATTACATAC[A/C/G]TGATTTATTTACATG | 23072 |
rs75240534 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43399815 | TAGGAATATAAAGTT[A/C]GTAGCTAGCGGAGCA | 23072 |
rs75241534 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43239166 | TGGCTGATGAATATT[C/T]GCTGTGACATCAGCC | 23072 |
rs75250832 | snp | A/C/T | 0.0869089 | 0.189476 | intron-variant | HECW1 | GRCh38.p7 | 7:43467247 | GTGACAGGACCAGGC[A/C/T]GAACTGAGGGAGGAC | 23072 |
rs75274682 | snp | C/G | 0.119281 | 0.213102 | intron-variant | HECW1 | GRCh38.p7 | 7:43532269 | CTCTGACCTCCTCAC[C/G]TCCACTACCACCCCC | 23072 |
rs75278768 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | HECW1 | GRCh38.p7 | 7:43217072 | CCATTTTAATAGCTC[A/C]TTCTCTGATCACACT | 23072 |
rs75280131 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43323860 | GGCAACATGGTGAAA[C/T]CCCGTCTCTACTAAA | 23072 |
rs75280456 | snp | A/G | 0.178144 | 0.239451 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298793 | AATGAGCTGGTCTCC[A/G]TTGCCACCACTTACC | 23072 |
rs75281704 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301874 | GAGTGGAAACTCTGT[A/C]AAAAAAAAAAAAAAA | 23072 |
rs75282349 | snp | A/C | 0.191147 | 0.242974 | intron-variant | HECW1 | GRCh38.p7 | 7:43495753 | CAGAGTCATATTCAG[A/C]CACCTGGGTCATTCA | 23072 |
rs75285302 | snp | A/G | 0.244776 | 0.249945 | intron-variant | HECW1 | GRCh38.p7 | 7:43484354 | TGTGAAAATAGCAGG[A/G]TATCTGATTAGATAT | 23072 |
rs75295403 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43378292 | AGGTGATTTTGCTCT[C/G]CTGTGTACACAGTGA | 23072 |
rs75314626 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43450590 | AGACTCAAATCCTAC[A/G]TATTGGACTGTGTGG | 23072 |
rs75316721 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | HECW1 | GRCh38.p7 | 7:43336668 | ATATTGAATATTGAA[C/T]TCAATAAGTAATTTT | 23072 |
rs75317928 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43370888 | TAGGGCAATGATATT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs75329255 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269911 | AATGCATGGGACAAC[C/T]GCCATAACAAAGAAT | 23072 |
rs75331412 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43548328 | AATTGTTGTAAGTCT[A/C]CAAAAAAATTCCCAA | 23072 |
rs75331808 | snp | A/G | 0.067446 | 0.170804 | intron-variant | HECW1 | GRCh38.p7 | 7:43334415 | AGATGTCTCTGTCTC[A/G]TGTATCACACGTTCC | 23072 |
rs75332670 | snp | A/C/T | 0.0310518 | 0.120672 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299097 | CTATTACCGTATCCT[A/C/T]GAGGCCAGAGATGTC | 23072 |
rs75333813 | snp | A/T | 0.175254 | 0.238565 | intron-variant | HECW1 | GRCh38.p7 | 7:43325820 | TTTCCTCGTGTGGAA[A/T]CCTGGCTGGATGCAC | 23072 |
rs75344053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286766 | AAAAGTCATAGTCTC[A/G]GCCTACATAGACTTT | 23072 |
rs75376470 | snp | A/C/T | 0.0372196 | 0.131242 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158877 | ACCCTGACTTATGCA[A/C/T]CAAGAGAGAGGTTCT | 23072 |
rs75384009 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | HECW1 | GRCh38.p7 | 7:43273544 | AAAACTTTAAGATAT[A/G]TTTCCTCTTTTACCC | 23072 |
rs75399458 | snp | A/G | 0.177182 | 0.23916 | intron-variant | HECW1 | GRCh38.p7 | 7:43504313 | ATCATCTCCACAATC[A/G]CTAATTCAAACCTCC | 23072 |
rs75401048 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43338871 | TTTTAGTGCAATCCC[A/T]CTGGAGATAAATAGT | 23072 |
rs75406256 | snp | C/G | 0.213635 | 0.247341 | intron-variant | HECW1 | GRCh38.p7 | 7:43364680 | GGGTGAGAAATGGCT[C/G]AGGCCTGGCAGGGAA | 23072 |
rs75417226 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HECW1 | GRCh38.p7 | 7:43450373 | AACAGCCTTTCGGCA[A/G]CCCTGTGATGAAACC | 23072 |
rs75419983 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43304636 | AGCTGGGATTACAGA[A/C]ACGTGTCACCACACA | 23072 |
rs75430678 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43223997 | CTCTTCCCGCTCCCA[C/T]ATTCATGTATCATTG | 23072 |
rs75443998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119340 | CACTCTTTTCTTAAG[C/T]ACCTGGCTTCTTCCA | 23072 |
rs75449119 | snp | A/G | 0.122758 | 0.215196 | intron-variant | HECW1 | GRCh38.p7 | 7:43534651 | CAGACATTTTCTGTG[A/G]GTTTGTATAGTTGCG | 23072 |
rs75454649 | snp | A/T | 0.031825 | 0.122064 | intron-variant | HECW1 | GRCh38.p7 | 7:43314831 | CACATTTTCCGTGCT[A/T]TGCCAGAGATCAAAT | 23072 |
rs75481540 | snp | A/G | 0.084364 | 0.187256 | intron-variant | HECW1 | GRCh38.p7 | 7:43482547 | GAATATGGTTGAGTG[A/G]CAAGAGAGATGTTAG | 23072 |
rs75490371 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | HECW1 | GRCh38.p7 | 7:43218021 | AATGGGGGCACAGCA[C/T]CAGCTAGGTATTAGG | 23072 |
rs75511379 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43290539 | AGGGGGTATAACGAG[A/G]CATGTCTGGCCTCCC | 23072 |
rs75518482 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43431893 | TGCTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA | 23072 |
rs75529437 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | HECW1 | GRCh38.p7 | 7:43170581 | GGACAGCACACTCTC[A/T]CTGGCAGAGGTCAGG | 23072 |
rs75530205 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43201339 | GAGCTGAGGCTGCGG[A/G]AGTCCATGAGACTGT | 23072 |
rs75552906 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43291087 | ACGCTGTTATATGTA[C/T]AATGTTTATTTAGAA | 23072 |
rs75570699 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | HECW1 | GRCh38.p7 | 7:43448779 | CTTTCTCTACAATTA[A/G]GTTATATTATTTATA | 23072 |
rs75594380 | snp | C/T | 0.079617 | 0.182947 | intron-variant | HECW1 | GRCh38.p7 | 7:43446282 | ATTAGTTTTAAAACG[C/T]ATTCTGTGTTTTAAC | 23072 |
rs75609225 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43327376 | CCCACTTTAGCACTA[C/T]GCTAAATTGAAATCA | 23072 |
rs75615949 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | HECW1 | GRCh38.p7 | 7:43267312 | TACAATTAGACATTA[A/G]TGATTTTTAAAATTT | 23072 |
rs75617050 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43346429 | ACAACCCACAAAATG[C/T]GAGAAAATATTTGCA | 23072 |
rs75629356 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | HECW1 | GRCh38.p7 | 7:43531768 | TTCCTGCACCATGCG[C/T]TCCACATCCCTGTTC | 23072 |
rs75631973 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | HECW1 | GRCh38.p7 | 7:43321918 | CTCCCGGCAATGACA[C/G]CAATAGCTCTTTCTT | 23072 |
rs75640263 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43281170 | AAGAGCACTGCTGAG[A/C]GTCCCTTCAGCAGCC | 23072 |
rs75660937 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | HECW1 | GRCh38.p7 | 7:43332598 | AAGCTGATCACCACG[G/T]TGTCCAATTACACAG | 23072 |
rs75662532 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359805 | CAAATTGGAGATTTC[C/T]CATATTGTTTCAAAC | 23072 |
rs75662619 | snp | A/G | 0.175254 | 0.238565 | intron-variant | HECW1 | GRCh38.p7 | 7:43325817 | TCGTTTCCTCGTGTG[A/G]AAACCTGGCTGGATG | 23072 |
rs75673228 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | HECW1 | GRCh38.p7 | 7:43245248 | AGCTCAGCAAAGCCT[C/T]GATTTCCCCAGTTCA | 23072 |
rs75679582 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | HECW1 | GRCh38.p7 | 7:43225307 | GAACTGCACAGATGG[C/T]GGGAGAATCAACTCT | 23072 |
rs75683723 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506977 | CGGGAGGCTGAAGTA[C/G]CAGAATCGCTTGAAC | 23072 |
rs75689516 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529117 | ACCTCATTATCACCC[A/C]GAACTGTGCCATGTC | 23072 |
rs75695146 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376866 | GCAAGGACTCTGTCT[A/C]AAAAAAAAAAGACAT | 23072 |
rs75695689 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43356968 | AGAAGACAGACAAAT[A/G]GCCAACAGATGCATG | 23072 |
rs75702545 | snp | G/T | 0.216349 | 0.247725 | intron-variant | HECW1 | GRCh38.p7 | 7:43462065 | GGTCAAGGAAAGAGC[G/T]GGGCACTGGTCTGCA | 23072 |
rs75704653 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43325851 | ACCCAGATTGCTGCA[C/T]GCTGTGGTCTCATCA | 23072 |
rs75709371 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43233454 | GTGTCTGTAGAATCT[G/T]AAAATATTATCCAGT | 23072 |
rs75719772 | snp | A/G | 0.0573587 | 0.15934 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43377532 | AAGGTGCTGTAGATT[A/G]AGACAGGACTGGTGC | 23072 |
rs75728591 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43176953 | GCCTCTTCCTGAGAT[A/C]CCTTAGATTACTATT | 23072 |
rs75728843 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | HECW1 | GRCh38.p7 | 7:43553467 | CAGATTGCTTGAACT[C/T]ATAAGTTCGAGACCA | 23072 |
rs75749011 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213353 | GTTTGGATCATCTGT[A/G]TACTACTGATGATAA | 23072 |
rs75752341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192294 | AGTAGGGTGACTCAT[G/T]AACATTAATTGGTTA | 23072 |
rs75761039 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43524963 | TTCACGAGAATCAGC[A/G]TTAATTAACTTGAGC | 23072 |
rs75771578 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283449 | ACTTTTTTTAATTTT[A/G]GAAAATGTATTTATT | 23072 |
rs75786057 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43358167 | TGGCCCCTCCATGCT[G/T]ATCCCACCGGCACCT | 23072 |
rs75786484 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159524 | TTCTAAAAAGTAGAA[C/G]TTGGGCACAGGTATA | 23072 |
rs75786724 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43305380 | GAAGCTCAGAGAAGT[A/G]TCTGAATCTCAATTA | 23072 |
rs75794393 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | HECW1 | GRCh38.p7 | 7:43531671 | TGCACCCCTAATGAA[A/G]ATTGCCAAAACCATC | 23072 |
rs75797657 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HECW1 | GRCh38.p7 | 7:43426912 | AAATATATGCAAAAC[A/G]TGGAAGCTGTATCTC | 23072 |
rs75799602 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43433932 | CCCAAGGATGCCCAG[G/T]ATTGGCTTTGTCATT | 23072 |
rs75824139 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43469946 | CATCAATGTCCCCTC[A/G]AAGCCATGAGTCTCT | 23072 |
rs75828917 | snp | A/G | 0.1652 | 0.235179 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510113 | AACGTGCCCTTTGTT[A/G]CCCCAGAACTTGTGA | 23072 |
rs75829822 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | HECW1 | GRCh38.p7 | 7:43534438 | GAAGAGGGAGAGAAG[A/G]AAGGGAGAGGGAGAC | 23072 |
rs75848164 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43254143 | GTAATGAATATCCCC[A/G]GATTAGATGAACAAT | 23072 |
rs75866462 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43466983 | CTTTTGATATGGTTT[C/T]TTCGAATATCGTGCT | 23072 |
rs75870777 | snp | C/G | 0.224116 | 0.248656 | intron-variant | HECW1 | GRCh38.p7 | 7:43485728 | AGTACACCTGTATAG[C/G]ATACTTACAGTGAAT | 23072 |
rs75897845 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43485225 | CTTTGCAGTGAGCTT[A/C]TTTGATGGCAGAAGT | 23072 |
rs75913026 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157711 | TACTATAGGCACATG[C/G]CACCAAACCTGGCTA | 23072 |
rs75940971 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | HECW1 | GRCh38.p7 | 7:43222589 | GCTACTGCTGAATTA[C/G]AGTCTAAAGATACTG | 23072 |
rs75944208 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43291996 | CCTTCTCCATTAATT[C/T]AGTCTCTAGTGATTC | 23072 |
rs75949354 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | HECW1 | GRCh38.p7 | 7:43287539 | GACAGGGTCTCACTA[C/T]ATTGCCCAGGCTGGT | 23072 |
rs75950135 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269838 | TGGAGGCATTTTTTG[A/G]TTTTTGCAATTGGGT | 23072 |
rs75976101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43409806 | GCAAAACTGTCCATT[C/T]AACCCCTAAATTGTA | 23072 |
rs75999729 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515428 | GGCTAGTGAAATAGT[C/T]GTAGGAAGAGATATT | 23072 |
rs76003749 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43273066 | AAGCAAATTAGTGCA[G/T]GAACAGAAAACCAAA | 23072 |
rs76024712 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43369868 | TGGATGAGTTCACAG[C/G]TGAAGTCTTTCAAAT | 23072 |
rs76050272 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360012 | TTAGTCATCACATCA[G/T]CACAATCACTAACAT | 23072 |
rs76050353 | snp | A/G | 0.0379877 | 0.132479 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562390 | ACCAACTCCAGAACT[A/G]GGAGCTGATCAACTC | 23072 |
rs76060634 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43223621 | CAAAACTCCGTCTCA[A/C]AAAAAAAAAAATATG | 23072 |
rs76075983 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43420581 | GTAAACAGTACAAAA[C/G]ATTACCCAAACTACC | 23072 |
rs76078729 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43469787 | TGAACCTGTGTAACC[G/T]TCTATGAACTTTACC | 23072 |
rs76081187 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43387672 | GCTTATGGTATATTT[A/G]TAACTCTTCTAAGCT | 23072 |
rs76083147 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43388361 | CTGCAAATTCAAAAG[C/T]TTCCAGGGAGCCAGG | 23072 |
rs76087854 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43504118 | TCAAGGCCTGTGGCC[C/T]CTGCCTTGTAGTCTT | 23072 |
rs76106206 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260932 | TATTCTAAGAAAGTT[G/T]GCAAACATTAACCTC | 23072 |
rs76117575 | snp | A/G | 0.200492 | 0.245049 | intron-variant | HECW1 | GRCh38.p7 | 7:43366682 | CAGGTTCCAATAAAC[A/G]TCAATCACCATGTAT | 23072 |
rs76125586 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43403756 | TATGTTCTCAACTAC[A/G]CAAAGAAAAATACTA | 23072 |
rs76127927 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43423250 | AGCAGTTTCACAAAT[G/T]ATTTTTTAAGTTCCC | 23072 |
rs76133870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43488588 | TCAGTTGCTGTCAGA[C/T]GTCCCTCGGGATGGA | 23072 |
rs76139231 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43305078 | CCCCTAGAAGTGACT[A/G]AGCCAGGTAGACTTT | 23072 |
rs76149994 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136663 | GGAAGATTTCCAGCC[C/T]GTTTTCATCTAAATT | 23072 |
rs76168312 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43498441 | GGAGAGCATATAGAT[C/T]TGAGGTCATTCATAA | 23072 |
rs76171229 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43169451 | TCTCCAGACATTGAC[A/G]GATACCCCTGGGAGA | 23072 |
rs76196235 | snp | C/T | | | missense | HECW1 | GRCh38.p7 | 7:43561829 | GGGCACACACATGCT[C/T]CAACCGACTGGATCT | 23072 |
rs76203735 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43340538 | TAATTACCTTTGAAC[C/T]GTGCAAGCAATAGCC | 23072 |
rs76205128 | snp | A/G | 0.191147 | 0.242974 | intron-variant | HECW1 | GRCh38.p7 | 7:43495085 | CTTCCTGATGTTACC[A/G]TGGCATTTGTTTTTT | 23072 |
rs76207213 | snp | A/C | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269809 | TTACCTCTGAGGAGA[A/C]AATTGGCAATGTCTG | 23072 |
rs76213770 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281713 | CTCTTTCTTTGCTTT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs76236867 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43261982 | TCCCAGCTCTGTGTG[A/G]AGCCAAGGCAGGAGA | 23072 |
rs76260863 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43460484 | TGATTGGTTTGGCTT[G/T]GTTTTGGAGGGCTTT | 23072 |
rs76266281 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43232392 | AATTCAGAAGAAGAG[C/T]AGAAATGGAGGCTGG | 23072 |
rs76266372 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43356870 | TACCAAAATGTATGC[A/G]GTATAGTAAACAACT | 23072 |
rs76272610 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43457801 | AACAAACAAAAAACA[A/T]GGAAACAAAAAAATA | 23072 |
rs76278852 | snp | A/C | 0.187369 | 0.242028 | intron-variant, downstream-variant-500B | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43151217 | TGCAGCTGGCTACAC[A/C]TTTTCTTCCCCAGGT | 23072 |
rs76311481 | snp | A/C | 0.107341 | 0.205301 | intron-variant | HECW1 | GRCh38.p7 | 7:43259236 | TACTAAAAATACAAA[A/C]ATTAGCCAGGTGTGG | 23072 |
rs76320323 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | HECW1 | GRCh38.p7 | 7:43238486 | TTAGAACTGTTCCTC[G/T]AGGGACAAACTGGAT | 23072 |
rs76336492 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43366102 | AGCAAGACTGTCTCA[A/C]AAAAAAAAAAAAGAA | 23072 |
rs76338001 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | HECW1 | GRCh38.p7 | 7:43529709 | CCACTCAAGTTGGAC[C/T]TGCCCACTCAGGCTC | 23072 |
rs76344233 | snp | A/G | 0.131723 | 0.220251 | intron-variant | HECW1 | GRCh38.p7 | 7:43504350 | CTTCCAATGTGCTTG[A/G]TCCACTACCCTTCCT | 23072 |
rs76346215 | snp | A/G | 0.214239 | 0.247429 | intron-variant | HECW1 | GRCh38.p7 | 7:43457466 | AAAGGAGGAGAAACA[A/G]TTTAGTCCTATTAAA | 23072 |
rs76346411 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43339550 | AAAGTCTTTGCCAGA[C/T]GACTTCAGCATCAGG | 23072 |
rs76358585 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43557088 | AAGATCAAAGAACCT[-/A]AAAAAAATGTCATCT | 23072 |
rs76382842 | in-del | -/A | 0.34303 | 0.232046 | intron-variant | HECW1 | GRCh38.p7 | 7:43287471 | CATGGAAGGTTTGGC[-/A]AGAGGGGATGTGATC | 23072 |
rs76384179 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141234 | TTGAATCCACTGAGT[A/G]GGGTCATTAGGAAAC | 23072 |
rs76388573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43316398 | GATTTGCAATAGAGG[A/G]CCCTATTTTTGGCCC | 23072 |
rs76404578 | snp | A/G | 0.204803 | 0.245881 | intron-variant | HECW1 | GRCh38.p7 | 7:43178312 | CACCTGGCCAGCAGG[A/G]TTCTATCTAACTATC | 23072 |
rs76418378 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | HECW1 | GRCh38.p7 | 7:43433166 | TCCATTAATAAGAAT[A/G]CCAACAAAAAATAAG | 23072 |
rs76418758 | snp | C/T | 0.0391387 | 0.134304 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563444 | CAAGAGACCCCACTA[C/T]TTAAATGTCATTTAA | 23072 |
rs76429718 | snp | A/C | 0.19646 | 0.2442 | intron-variant | HECW1 | GRCh38.p7 | 7:43456035 | AAGTATTAGAATTTT[A/C]ACATAGGTGTTGATC | 23072 |
rs76434552 | snp | G/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514742 | AATTAAGCTAAATAA[G/T]GAAGGATCCATTGAG | 23072 |
rs76436824 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | HECW1 | GRCh38.p7 | 7:43332933 | GGAAGATAATTCAAC[C/T]GGTCCCATAGTCACA | 23072 |
rs76443536 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43226676 | CAGGAGATGGGTGAG[A/G]AAAGAGCCTGTGAGG | 23072 |
rs76445158 | in-del | -/AA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361855 | TTACATTAAAAAAAA[-/AA]CAGGCCAGGCGCAGT | 23072 |
rs76455899 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43436163 | AACTAGACTTTGTCT[A/C]AAAAAAAAAAAAAAA | 23072 |
rs76456089 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43390560 | AAAACAAAAAAAAAA[A/C]AGCAGAGTTGTGGAG | 23072 |
rs76459581 | snp | C/T | 0.00385496 | 0.0437335 | intron-variant | HECW1 | GRCh38.p7 | 7:43360997 | TAAGTCTCATTTCTC[C/T]GTCTTTGGTTAGACC | 23072 |
rs76460547 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43178314 | CCTGGCCAGCAGGGT[C/T]CTATCTAACTATCCC | 23072 |
rs76464744 | snp | A/G | 0.031825 | 0.122064 | intron-variant | HECW1 | GRCh38.p7 | 7:43465789 | GCAGCTACTCAGCAG[A/G]CTGAGTATCTGGGAG | 23072 |
rs76493614 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156738 | CCTGTTCACCTTAGG[C/T]GTGGTCATGTGATCT | 23072 |
rs76501094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286227 | AGCACAGTCCAAACA[A/G]ACAAGTTTCCCTTGA | 23072 |
rs76531508 | snp | A/T | 0.0547245 | 0.156101 | intron-variant | HECW1 | GRCh38.p7 | 7:43389513 | TGTTAGAGAAGAATC[A/T]CTTTACACCCTAAGA | 23072 |
rs76552426 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43244927 | TGTGTGCCTTGGTAC[A/G]CGTCAGCGGGCGGGA | 23072 |
rs76552943 | snp | A/G | | | missense | HECW1 | GRCh38.p7 | 7:43550542 | TGAAGTGGCGGGTGG[A/G]GCGCGGCGTGGTACA | 23072 |
rs76573375 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43215893 | TTCTGGTCACTGCTG[A/T]GTCTCCAAGGACGTA | 23072 |
rs76578825 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43529442 | CCTGGAGAAAATGAA[A/G]TAATTCCAAGAAAGG | 23072 |
rs76583755 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119648 | TCCCTTTGAATGGCA[C/T]GTTAGCTTAAAATTA | 23072 |
rs76604335 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43475878 | TTTTAAAAACAAATA[C/T]TCTTGGTAAACTAAG | 23072 |
rs76605188 | snp | A/G | 0.220544 | 0.248259 | intron-variant | HECW1 | GRCh38.p7 | 7:43417529 | TTTCACTGGATATAG[A/G]ATTCTGGGTTAACTG | 23072 |
rs76609090 | snp | A/G | 0.120326 | 0.21374 | intron-variant | HECW1 | GRCh38.p7 | 7:43493949 | CTTACTTGAGGATGT[A/G]TAAAGGTTAAGGCAG | 23072 |
rs76618925 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43170957 | CCAGGGGAAACATGA[A/C]TGAAACCAGTGTCCT | 23072 |
rs76626240 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43334678 | GAGAAAGTCATCCTT[A/G]TTTTATTGTCATTAG | 23072 |
rs76627093 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43368658 | TATCCTAGCCCAACA[G/T]TAAGGAATCTGTTCA | 23072 |
rs76627325 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43552547 | GGAAACCCTGTACCC[A/C]TGAAGCAGTTGCTCT | 23072 |
rs76632102 | snp | G/T | 0.192088 | 0.2432 | intron-variant | HECW1 | GRCh38.p7 | 7:43478056 | AGAGATAATTTTAAA[G/T]TTAAAGAACAATGTT | 23072 |
rs76636397 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | HECW1 | GRCh38.p7 | 7:43279558 | TTAGTTCCTTGAACC[C/T]GTTGGGAATTCCCAT | 23072 |
rs76642821 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519992 | CATGCCAGGAGAAGC[C/T]AAAGTCTATATAAAA | 23072 |
rs76643590 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43266127 | CAGTCTCTACCCCTT[C/T]CCATTCTCCCAAGGT | 23072 |
rs76660499 | snp | C/T | 0.17654 | 0.238964 | intron-variant | HECW1 | GRCh38.p7 | 7:43332221 | TAAATAAATAAAAAG[C/T]TTCTCCTCTTCCTCT | 23072 |
rs76660856 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43335783 | TTTTCTTTCTTCCTT[C/T]CTTCCTTCCTTCCTT | 23072 |
rs76662801 | in-del | -/TAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372427 | GGTTTGTTACATATG[-/TAT]ACACATGTATACATG | 23072 |
rs76670573 | snp | A/G | 0.131381 | 0.220067 | intron-variant | HECW1 | GRCh38.p7 | 7:43252275 | CAGGTTTCTGCCCCC[A/G]GTCAGTATCCGTGTC | 23072 |
rs76676023 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43271308 | AGAACTGGAACAAGA[A/C]AAGGATACAACTCTC | 23072 |
rs76686144 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43244243 | CTACTTCCAGAATTA[A/C]AGCTGAGAGCTCCGC | 23072 |
rs76707085 | snp | G/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269923 | AACCGCCATAACAAA[G/T]AATTATCTGGCTCAA | 23072 |
rs76718484 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43185332 | CAATAAACTGGTAAA[C/T]GTAAGTAAAGTGTTT | 23072 |
rs76718729 | snp | A/C | 0.0883596 | 0.190715 | intron-variant | HECW1 | GRCh38.p7 | 7:43402835 | TGTTTTTACCACTGC[A/C]TGGAGGTAATACATT | 23072 |
rs76728146 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | HECW1 | GRCh38.p7 | 7:43505980 | AAGCCTTGATTCTGA[A/C]CACCTTTAAAACTTG | 23072 |
rs76733124 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361061 | TCTTGTGCGTGCGTG[C/T]GTGTGTGTGTGTGTG | 23072 |
rs76740961 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | HECW1 | GRCh38.p7 | 7:43225811 | TTTTTTTGGGACAGG[G/T]TCTCACTGTGTCACC | 23072 |
rs76753466 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43456006 | ACTCTGTCTCAAAAA[A/G]AAAAAAAAAAAGAAA | 23072 |
rs76764444 | snp | A/G | 0.18989 | 0.242666 | intron-variant | HECW1 | GRCh38.p7 | 7:43497217 | CTTGAGATGCAAAGT[A/G]GAGATCAGGGAGAGA | 23072 |
rs76775805 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121722 | CACTCAGTTTCCTAA[G/T]AGGATATGATTTATC | 23072 |
rs76776336 | snp | A/G | 0.137867 | 0.223442 | intron-variant | HECW1 | GRCh38.p7 | 7:43337007 | CTGCAATAAACATAG[A/G]AGTGCAGATGTCTTT | 23072 |
rs76779295 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43188813 | GAAGAACTGGGGATA[C/T]TTGGCCAACAGTACA | 23072 |
rs76783388 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43384809 | TATGCAAAATGCAGC[C/T]CTTGTCTTCACTAAG | 23072 |
rs76789227 | snp | A/T | 0.191147 | 0.242974 | intron-variant | HECW1 | GRCh38.p7 | 7:43490779 | TGTTTTGTTTTTGAG[A/T]TAGAGTCTTGCTGTG | 23072 |
rs76790584 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302843 | CAGTATTTCCTAACA[C/T]TGAGAAGGGAAAAAT | 23072 |
rs76806302 | snp | G/T | 0.00588035 | 0.0539036 | intron-variant | HECW1 | GRCh38.p7 | 7:43463814 | GGTATTGGAGGAGGG[G/T]TCCCCACAACCTGTG | 23072 |
rs76807719 | snp | C/G | 0.0737376 | 0.17729 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128596 | TTTCATGCCTGCCAA[C/G]ATAACACATTCTGCA | 23072 |
rs76816064 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43327253 | CTGTTAGGAAAAAGT[A/C]TGACTCCATATACAT | 23072 |
rs76852295 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | HECW1 | GRCh38.p7 | 7:43427671 | ACAACCTGCGTTCTC[A/G]GCTCAGGATCTCAGA | 23072 |
rs76871848 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198735 | TGCACACWCWCACAC[C/T]CCACACTCTCACACA | 23072 |
rs76872397 | snp | A/G | 0.166832 | 0.235761 | intron-variant | HECW1 | GRCh38.p7 | 7:43402176 | TGATTCTTCCTGGAC[A/G]CCAGACAAGGATCCA | 23072 |
rs76879900 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43169913 | GCTGATTGATTTTGA[A/G]CCTCTAGGGTAGCAC | 23072 |
rs76896637 | snp | A/C | 0.046775 | 0.145601 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111087 | AAACATCTCTGAGCC[A/C]AGTTGATGCTGATTC | 23072 |
rs76896883 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43184128 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 23072 |
rs76903407 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135214 | CTTCCTTACAGGGAG[C/G]GGGTAGTCATATGAC | 23072 |
rs76916583 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43507456 | GAAGGGAAGCAGGAA[C/G]AGAAGGTAAGAGAGG | 23072 |
rs76922785 | snp | A/G | 0.190205 | 0.242744 | intron-variant | HECW1 | GRCh38.p7 | 7:43497285 | AGGTGAAAAATGAAA[A/G]AAAGCTAGTGTGGCC | 23072 |
rs76926365 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | HECW1 | GRCh38.p7 | 7:43250152 | GCACACACACATACA[C/T]ACACACACAGAAATA | 23072 |
rs76928591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43325038 | GAAAGTACCATCAAA[C/T]TAGGAATATTTTAAA | 23072 |
rs76933086 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43477534 | TCCTTGTATTTTTGA[C/T]GTCACTAGTGTCATT | 23072 |
rs76949961 | snp | A/G | 0.264084 | 0.249603 | intron-variant | HECW1 | GRCh38.p7 | 7:43366881 | CAGTGAGATGGACCC[A/G]CCCCCTGAGATCCCG | 23072 |
rs76968924 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43386737 | GTCCATGGACTCTCA[A/G]ATCAGCTCAGATGAG | 23072 |
rs76976176 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43485717 | ATTTAAAAAATAGTA[C/T]ACCTGTATAGGATAC | 23072 |
rs76987201 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43224305 | GTAAGACATTATCCC[G/T]GCATCTCTAAGTTCA | 23072 |
rs76993976 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43315198 | CCCAACTCTTGAAGA[A/G]TTAAAGTTTTTCCTT | 23072 |
rs76994767 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43187554 | TACTCATTCTAAAAT[C/T]GTTTTTGTGACTTCT | 23072 |
rs77002406 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | HECW1 | GRCh38.p7 | 7:43235450 | GGAATAAGAGAGGCA[C/T]CCTTGGCCCAAGCCT | 23072 |
rs77007129 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | HECW1 | GRCh38.p7 | 7:43551880 | TCTGGTTCATAGATG[A/G]TACCTTCTCCCTGTG | 23072 |
rs77008358 | snp | A/G | 0.25214 | 0.249991 | intron-variant | HECW1 | GRCh38.p7 | 7:43240882 | TCCTATTGCTGTGCC[A/G]CAAGGGTCTGCAGAG | 23072 |
rs77018286 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43275463 | TTTGGTTTTCTCTGA[A/T]TGCTTCTTAAAAAAT | 23072 |
rs77025398 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43178129 | ATTCTGCTTCAGCCT[C/T]CAAAGTAGCTGGTAC | 23072 |
rs77031619 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43315030 | GGGCCATGGCACATC[C/T]GTGTGCCATCAAATG | 23072 |
rs77049622 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43475024 | TACAGTGTTTCAATT[C/T]GGGAAGGTGAAAAAG | 23072 |
rs77055342 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43390144 | CCTCGTAGTGATTAG[C/T]ATAAGAGCCCTGAAA | 23072 |
rs77056379 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43367051 | TCATTTTCCTCAACT[C/T]GTAAGAAAATGGGGC | 23072 |
rs77063631 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43368339 | AAATGTGCACACACC[A/C]CAGCCATGATTTCTG | 23072 |
rs77064351 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43447581 | TGCTGAAGGCCATGC[A/G]CACGCTGGCATGTGA | 23072 |
rs77073972 | snp | A/G | 0.198324 | 0.244601 | intron-variant | HECW1 | GRCh38.p7 | 7:43383851 | ATTAACATATTTTAT[A/G]TGTTATTTGTATTAT | 23072 |
rs77082033 | snp | A/G | 0.125874 | 0.217008 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115345 | AACATTTGGTGGAGG[A/G]TTGGGGAAAAGAGAA | 23072 |
rs77089726 | snp | A/G | 0.214541 | 0.247473 | intron-variant | HECW1 | GRCh38.p7 | 7:43458663 | TCCAGATTTTTCCAT[A/G]CTTAACCTATTGCTT | 23072 |
rs77093062 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301875 | AGTGGAAACTCTGTC[A/C]AAAAAAAAAAAAAAA | 23072 |
rs77096571 | snp | C/T | 0.213635 | 0.247341 | intron-variant | HECW1 | GRCh38.p7 | 7:43429847 | CTGTTTTTCATTTCC[C/T]CCCTTTATATCTCGC | 23072 |
rs77107244 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43543781 | CAAAACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 23072 |
rs77109663 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43280517 | AGTTTTGCCAGCTTG[C/T]CTTTTATTTGATGAA | 23072 |
rs77123694 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HECW1 | GRCh38.p7 | 7:43468504 | ATGTGGGCCAAGGGG[A/G]CATGATTCAATGCAC | 23072 |
rs77124832 | snp | A/G | 0.227369 | 0.248974 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144522 | TTGATTAGTTTACTC[A/G]CTTATTTTTGTCAGT | 23072 |
rs77130339 | snp | A/G | 0.039522 | 0.134904 | intron-variant | HECW1 | GRCh38.p7 | 7:43238005 | CTGCCCCATCATATT[A/G]CTTTTTGTAAAAGGA | 23072 |
rs77131115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43199024 | TCCAAAGCCTGGTAT[A/G]ACCACAAATCCGATA | 23072 |
rs77160882 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43382698 | AAGGATAGATGTGGG[G/T]GGAGGGGTTGGATAA | 23072 |
rs77167143 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157138 | AATAGGAGAGGCATG[C/T]GTATAAAAAAGTACC | 23072 |
rs77191951 | snp | C/T | 0.187369 | 0.242028 | intron-variant | HECW1 | GRCh38.p7 | 7:43191489 | GCCCAGCTGTCACCA[C/T]GTGTGTGCTTATAAC | 23072 |
rs77214302 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43531882 | ATTCAGCCCTGGGTC[C/T]GCCTCTCCATCTGCA | 23072 |
rs77221082 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43497960 | GTCAAGGAGGCAGTC[A/G]CCTGTCCTGTCCTGA | 23072 |
rs77254751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43506593 | GATGCCAGAATGTGC[C/T]TCTGTTGAGCTCTTG | 23072 |
rs77267545 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43457966 | AGTCATTAACAAAAA[C/T]CATAAAAGACTTGCA | 23072 |
rs77279758 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43323857 | CTGGCCAACATGGTG[A/G]AACCTCATCTCTACT | 23072 |
rs77285250 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43175744 | CAAGTCATGAACGCA[C/T]GGAGCTAACGTTTCA | 23072 |
rs77295150 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43252080 | CCTTAACACACAGAA[A/T]ATTTCCAAATGTGCA | 23072 |
rs77306917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43443496 | TACAGCTCACCAGAG[A/G]GACTGATTTTCTTTA | 23072 |
rs77310115 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43388990 | AGAAAGGAGTGGGGC[C/T]TGGACCAAGGTGCCA | 23072 |
rs77313818 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161814 | CCCTAATTCCCATAT[A/G]CACTTCTCTGCAAAG | 23072 |
rs77317678 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43446652 | CAGGAGCTAAAGTGA[A/G]CATTAAAAAAAATAA | 23072 |
rs77324599 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43505483 | CTATGCAAGGGCTTC[C/T]TACTACACTTAGCAT | 23072 |
rs77337599 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43175020 | AGGATTAGAACAGCT[A/C/T]GAGGTACCTATGGGC | 23072 |
rs77338530 | snp | C/T | 0.223522 | 0.248594 | intron-variant | HECW1 | GRCh38.p7 | 7:43487722 | CAGCACTTTGGGAGG[C/T]AGGGCAGGAGGATCT | 23072 |
rs77352497 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116746 | ACATTTGATGTTCAC[A/G]GACTTTTAGAGAAAA | 23072 |
rs77359551 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | HECW1 | GRCh38.p7 | 7:43288778 | AGTCCATTTTGCCCT[A/G]TTATTCTCCACTCTT | 23072 |
rs77363681 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43265662 | GACCAACTGGGTATC[C/T]AACAATTCAAATCAA | 23072 |
rs77372862 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467302 | GCATTCTTGGGGAGG[C/G]GGCTGAATTGAGTCC | 23072 |
rs77384600 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43211843 | ACCTCAGTTAAGAAT[A/C]AAGGGTGGTGTTAGA | 23072 |
rs77395404 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529118 | CCTCATTATCACCCA[G/T]AACTGTGCCATGTCA | 23072 |
rs77400196 | snp | A/T | 0.0818113 | 0.184966 | intron-variant | HECW1 | GRCh38.p7 | 7:43284928 | CCCCAGGTCTTATAA[A/T]GTGAAACTTTGAAGG | 23072 |
rs77411456 | in-del | -/TCACTC | 0.492823 | 0.0594727 | intron-variant | HECW1 | GRCh38.p7 | 7:43283268 | TTTTATTTGACCTTT[-/TCACTC]TCATTATCTCACGAG | 23072 |
rs77412333 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | HECW1 | GRCh38.p7 | 7:43245164 | CTTAAATTCCCCTTT[A/G]TCTCCTTGAGTATCC | 23072 |
rs77412622 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43410868 | CTCTTTCATTTATAT[A/G]TTGGTGAATTGCTTT | 23072 |
rs77423622 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43354200 | AATAAAAAAAAAAAA[A/G]GGCCAGACAGAGAAG | 23072 |
rs77426106 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43220353 | CCAGTAGAGACACTC[A/G]CCTGAGTCTTCACGT | 23072 |
rs77430393 | snp | A/G | 0.214843 | 0.247516 | intron-variant | HECW1 | GRCh38.p7 | 7:43424808 | AATTATCACTATACT[A/G]ATACCATGATTAATT | 23072 |
rs77439039 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43437147 | CTCTAGACATTTTCT[C/T]TGCAGTTCAAAGTAC | 23072 |
rs77455645 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43357243 | ATAGCAAAAGAAAGG[A/C]AATCAATATATCGAA | 23072 |
rs77463379 | snp | A/C | 0.105214 | 0.203807 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140085 | ATCTTTTTATTGTTA[A/C]ATTTATACTTATTTA | 23072 |
rs77469668 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43361857 | ACATTAAAAAAAAAA[A/C]AGGCCAGGCGCAGTG | 23072 |
rs77474456 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152204 | TGCATAATTTCTGGG[A/G]AAAAAAATGTTCAAG | 23072 |
rs77487817 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43323900 | TTAGCCAGGTGTGGT[A/G]GCATGTGCCTGTAGT | 23072 |
rs77500146 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43226599 | ATTCACAGACCAAAC[A/C]ATTAGGGTCTGTGTC | 23072 |
rs77503015 | snp | A/C | 0.196149 | 0.244131 | intron-variant | HECW1 | GRCh38.p7 | 7:43482426 | TGGCTTGCTATGAGC[A/C]CTGTGGAATGCAAAA | 23072 |
rs77511772 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HECW1 | GRCh38.p7 | 7:43529331 | CCTCCCTGCTCCATG[C/T]TTGCACCCCATCTGA | 23072 |
rs77513893 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43261424 | GATTTGTTCTCTTCT[A/G]TTTGCTCTTTCTCAC | 23072 |
rs77518570 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43246153 | AATAAAAAAAAAAAA[A/T]TTAGCTGGGCATGAT | 23072 |
rs77522179 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298169 | ATAGAGTGCACCATT[C/T]GCCCTGTCTGGAATA | 23072 |
rs77524209 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43236337 | GGGGGGAAAAGCTCA[A/T]ATGAAATAGTGTGAA | 23072 |
rs77546540 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43353846 | CATAGACAAAGCAAG[C/G]AAGAAAGACCACCAC | 23072 |
rs77576248 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43535006 | TGTCCTATACAGTAG[A/G]TGCCAATATGATTCC | 23072 |
rs77583698 | snp | A/G | 0.31503 | 0.241394 | intron-variant | HECW1 | GRCh38.p7 | 7:43547442 | ATCTCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 23072 |
rs77585946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43406325 | TCAACTCCTTTGGCA[C/T]TTGGTGGTCATTTTG | 23072 |
rs77592808 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43473646 | AAAAAAAGTAAGGAA[A/G]TGAGAATAGGGAAGA | 23072 |
rs77594380 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | HECW1 | GRCh38.p7 | 7:43482520 | TACAGAGTTAAGTAA[C/T]GAGAGAAATCAGAAT | 23072 |
rs77597674 | in-del | -/AAA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125782 | AAAAAAAAAAAAAGA[-/AAA]GTGAGGCATTAATAC | 23072 |
rs77607428 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | HECW1 | GRCh38.p7 | 7:43472827 | AATCAGACAAGCTTC[A/T]AATTTCCCATCCTAA | 23072 |
rs77622572 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43453153 | TGAAAAGTTTGCCCA[A/T]GTTGCTGTGTAGGGA | 23072 |
rs77624811 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | HECW1 | GRCh38.p7 | 7:43357705 | TGTAATTTATAATAT[A/G]TTTTTATATATTTAT | 23072 |
rs77651706 | snp | A/G | 0.205417 | 0.245993 | intron-variant | HECW1 | GRCh38.p7 | 7:43175273 | TCTTGTCATGAGAAC[A/G]TTCAGAATCCACTCT | 23072 |
rs77652048 | snp | C/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269486 | ATAACACTCTATTGT[C/T]GGAACCAGAAAGACA | 23072 |
rs77655170 | in-del | -/TT | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520657 | ACTTTAAGGTTTTTT[-/TT]AAAAAAAACACAAAG | 23072 |
rs77684281 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43174906 | TACTCATCTCTGTTT[C/T]GTTCTATTTAAAATT | 23072 |
rs77686324 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521231 | GATGAGGGCAGAGTC[A/G]TGAATGGGAGTAAGG | 23072 |
rs77700860 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | HECW1 | GRCh38.p7 | 7:43548542 | GTGGAGAGCAGAGGG[A/C]TGCAGGTGAAAGACA | 23072 |
rs77723516 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43451965 | CTGTTCTTGGTAATG[A/T]GCTGTACTTTACAGG | 23072 |
rs77734340 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110703 | TCAAGCAATTCCCCC[G/T]CCTCAGCCTCCTGAG | 23072 |
rs77734590 | snp | C/T | 0.172028 | 0.23753 | intron-variant | HECW1 | GRCh38.p7 | 7:43344848 | TTTATCAGAATTTCT[C/T]GGATTCAAAATTTCT | 23072 |
rs77736391 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132544 | TCTCTCTTTCTCTCT[C/T]TCTCTCTCTCCCTTC | 23072 |
rs77737235 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43233949 | TTGCAGCTTCTGGTA[A/C/T]GGGAAAGATAAGATA | 23072 |
rs77751337 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | HECW1 | GRCh38.p7 | 7:43362909 | GATGGGACTGGCCTG[G/T]TGGCTCAAGGCTCGT | 23072 |
rs77755857 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43212779 | TATTTCCAGTCATAT[G/T]TCTAATATTCTTTAA | 23072 |
rs77760129 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43449391 | AGAATTTGCTCAACA[A/G]ATAATGTTCTATATT | 23072 |
rs77760265 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | HECW1 | GRCh38.p7 | 7:43505196 | TTCATGCTCTTCCCC[C/G]ACAAATGTGTTCTTT | 23072 |
rs77765401 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43321097 | GACCAGGTCTTCTCA[A/G]CAGGCATCCTACCCT | 23072 |
rs77785784 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43201637 | TCACAATTCCACTTT[C/T]CAAGTCTTTTTCCTG | 23072 |
rs77786939 | snp | A/G | 0.0148617 | 0.0849117 | synonymous-codon, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509056 | ACTCTTTGAGTACTC[A/G]GCAAATGATACTTAC | 23072 |
rs77797925 | snp | G/T | 0.0391387 | 0.134304 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43113254 | CCCCCGCCCCTCAGC[G/T]CCCTCCCAGTGGCGA | 23072 |
rs77801021 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | HECW1 | GRCh38.p7 | 7:43228919 | AAAAACAAATGACAA[C/T]GAGGAATCTACCAAA | 23072 |
rs77847493 | snp | A/T | 0.106633 | 0.204807 | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43512862 | GGATTGACACGGTAC[A/T]CAGCTGTGGCTGGAG | 23072 |
rs77847815 | snp | C/G/T | 0.0276507 | 0.11484 | intron-variant | HECW1 | GRCh38.p7 | 7:43382695 | TGGAAGGATAGATGT[C/G/T]GGGGGAGGGGTTGGA | 23072 |
rs77863180 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43550041 | CCCAATACTTTGGAG[C/T]TGGGAGGATCAGTTA | 23072 |
rs77878760 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43452477 | ACCTTAGAAAAATTG[A/G]TAATGAATCCTACCA | 23072 |
rs77880657 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43275902 | GTTTTATAGTGTCAG[C/T]TCTTATTGAATTTTC | 23072 |
rs77906500 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43318078 | AGCACTATGTCTGGA[A/G]CAGAACAAAGTACCC | 23072 |
rs77908457 | snp | A/C | 0.0726307 | 0.176182 | intron-variant | HECW1 | GRCh38.p7 | 7:43208836 | CTTCCAGCATGGAAC[A/C]GGAGGTCTGGATTCA | 23072 |
rs77920269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43480023 | AAATGCACTGTCAGG[A/G]GATCCCTACACTTAT | 23072 |
rs77941088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529177 | CAATCATTCTACAGC[C/T]GGCGTTCCCACCTCC | 23072 |
rs77962581 | snp | A/G | 0.162253 | 0.234095 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516989 | GTATAGGGCAGCTCC[A/G]TTATAATCTTTTGAG | 23072 |
rs77977115 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | HECW1 | GRCh38.p7 | 7:43433167 | CCATTAATAAGAATG[C/T]CAACAAAAAATAAGC | 23072 |
rs78000177 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43488267 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 23072 |
rs78016010 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | HECW1 | GRCh38.p7 | 7:43275374 | ATACACATGCATGCA[C/T]TGAAAATAGAATGGA | 23072 |
rs78018809 | snp | G/T | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126089 | TTTTTTTTTTTTTTT[G/T]GGTTTTTACTCACCA | 23072 |
rs78019282 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298780 | GGGGCCTCGCTGCAA[G/T]GAGCTGGTCTCCGTT | 23072 |
rs78032097 | snp | C/T | 0.030665 | 0.119967 | intron-variant | HECW1 | GRCh38.p7 | 7:43378995 | TTGCTTATGGGGGGG[C/T]GGTGTGCCCTTGCTC | 23072 |
rs78033961 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506976 | TCGGGAGGCTGAAGT[A/C]GCAGAATCGCTTGAA | 23072 |
rs78037614 | snp | C/T | 0.0197763 | 0.0975112 | intron-variant | HECW1 | GRCh38.p7 | 7:43329977 | TGAAGATGACTGATA[C/T]AGACTGTGAGAAGAG | 23072 |
rs78038512 | snp | A/G | 0.031825 | 0.122064 | intron-variant | HECW1 | GRCh38.p7 | 7:43365354 | GAGGCCTGGGACTGC[A/G]GCCTCCAGATAGAAA | 23072 |
rs78043882 | snp | C/G | 0.164219 | 0.234823 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301483 | TCTCCGAGGCTATGA[C/G]CACTGTTTAAGTCCT | 23072 |
rs78057184 | snp | A/C | 0.0865458 | 0.189163 | intron-variant | HECW1 | GRCh38.p7 | 7:43272987 | TGGAATACTAGGCAG[A/C]CATAAAAAAGAATGA | 23072 |
rs78067456 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | HECW1 | GRCh38.p7 | 7:43327865 | GTAGAAAGAACATAA[A/T]AGTGATTAAAGAGCA | 23072 |
rs78070246 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43288391 | ATTCTTCTCTCTTGA[A/C]ATTTTTCTGCAAACA | 23072 |
rs78071595 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43265578 | TAAAACACCTTTTGT[C/T]GTCTTTTTTCTGACA | 23072 |
rs78072289 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130796 | TTGTGGCATTATGTC[A/G]GCATTTAAAACATTT | 23072 |
rs78079502 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283450 | CTTTTTTTAATTTTG[A/G]AAAATGTATTTATTT | 23072 |
rs78092192 | snp | C/T | 0.138546 | 0.223781 | intron-variant | HECW1 | GRCh38.p7 | 7:43332772 | ATAACACTAATAATA[C/T]CAGCAGCTAAACTTC | 23072 |
rs78094168 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43411242 | CCTTCTTTGACCCAT[A/G]GATTATTTTGAAATA | 23072 |
rs78097340 | snp | A/G | 0.267908 | 0.249358 | intron-variant | HECW1 | GRCh38.p7 | 7:43436057 | TAGTCCCAGCTACTC[A/G]GGAGGTTGAGGCAGG | 23072 |
rs78123799 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43546238 | TTTTTTTTTTTTTTT[G/T]TTTTGCCATATCCAC | 23072 |
rs78125239 | snp | C/T | 0.0383715 | 0.133092 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300722 | CTGCTGGTTCAACCC[C/T]ACTGTGTACTGATGA | 23072 |
rs78126085 | snp | A/T | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521808 | TTGAACCTGGGAGGC[A/T]GAGGTTGCAGTGAGC | 23072 |
rs78128195 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43466443 | TTGCTTCACTTTTTT[C/T]CAGATCTAAGGAGAG | 23072 |
rs78134133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136423 | GGGGGCCAATTCCAG[C/T]CCCAGGGCTGAGAGC | 23072 |
rs78137132 | snp | A/G | 0.0755793 | 0.179102 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118237 | TGTGTGAAAGAAAAA[A/G]AAAAGATCAAAATTC | 23072 |
rs78137631 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140759 | CATCTTCAGCAGAAA[C/T]TTATTTTCTCTCAGT | 23072 |
rs78150899 | in-del | -/TTTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546239 | TTTTTTTTTTTTTTT[-/TTTT]GCCATATCCACAGTC | 23072 |
rs78167579 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43484783 | ATAAAAAGATCGTTA[G/T]TTGACACTTTCACTT | 23072 |
rs78175136 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | HECW1 | GRCh38.p7 | 7:43237146 | AAGGAAGGAAGTAGG[A/T]AGGTAGGTAGGTAGG | 23072 |
rs78180753 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135443 | GGAGCTAGGGCTAAA[A/C]AAAACAGTCTGGGGT | 23072 |
rs78183326 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43467929 | AGCCTGTGGGATGCC[A/C]TGGGCTCAATTCCAA | 23072 |
rs78184164 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43259386 | AGTGAGACTCCATGT[A/C]CAAAAAAAAAAACCG | 23072 |
rs78190526 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43274137 | GAAAAGCGCGGGTGG[C/T]GGCAGGCACGGAAAG | 23072 |
rs78192149 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43239067 | CAACTCATGCTGATG[A/G]AATCAAGGTCACAAA | 23072 |
rs78207718 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43481747 | CCCAGCACTTTAGGA[A/G]GTCGAGGCAGGCAGA | 23072 |
rs78211048 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43244934 | CTTGGTACGCGTCAG[C/T]GGGCGGGAAGATGAG | 23072 |
rs78213822 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43186689 | AAAAAAAAAAAAAAA[A/G]GATTATCATACCATA | 23072 |
rs78222642 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155131 | GGCTAACTTGTAGCA[C/T]GACTTTCAAAATAAC | 23072 |
rs78224160 | snp | A/G | 0.178785 | 0.239642 | intron-variant | HECW1 | GRCh38.p7 | 7:43500914 | TAGTAACTGCAACGC[A/G]AGTGGGACCCCACCC | 23072 |
rs78236432 | in-del | -/TA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162892 | CTCTCAACAACTCTA[-/TA]AAGAGGCAACTATTG | 23072 |
rs78262236 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426983 | CTACTATCTCTTTTT[A/C]TTAATCTGATGCCTT | 23072 |
rs78276046 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | HECW1 | GRCh38.p7 | 7:43276863 | AGTCAACCACCTGAA[C/G]CATACAGAATGCTCT | 23072 |
rs78286853 | snp | A/G | 0.192401 | 0.243274 | intron-variant | HECW1 | GRCh38.p7 | 7:43389907 | CAAAGCGCTGAGATT[A/G]CAGGTGTGAGCCACC | 23072 |
rs78292671 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514958 | GCTCTATCATCAGGA[G/T]CTAGCCCCCATTCAA | 23072 |
rs78303262 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43295306 | TTTATAATTGTGAGG[G/T]GGGTATATGGCTTTT | 23072 |
rs78303700 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43270695 | GAAAAAATCAATATA[C/G]CATTTGCAGATGTTT | 23072 |
rs78309855 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123333 | TCGTGACATTCTTGG[C/G]TTAAACTTAATTTTA | 23072 |
rs78319396 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | HECW1 | GRCh38.p7 | 7:43207339 | ATGTGAGCCACCGCA[C/G]GCCGCCTAAAATTCT | 23072 |
rs78330737 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43237873 | CTGCAAAAGCGCTGA[A/G]TAGGACTTAGTCTGC | 23072 |
rs78332966 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513657 | CGTTAAGTAAGCTGG[A/G]AAAAAAAACTGTTTG | 23072 |
rs78356364 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43404371 | CTCCCAAAGCTAAGA[C/T]ATAAATTCAATGCAG | 23072 |
rs78360250 | snp | A/G | 0.209693 | 0.246729 | intron-variant | HECW1 | GRCh38.p7 | 7:43370513 | TGGTATTCACCCAAC[A/G]GAGTTGAAAACTTAT | 23072 |
rs78363119 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297721 | GTTTATAAGATGGCA[A/T]TTTAAACATATATAC | 23072 |
rs78386728 | snp | C/T | 0.0379877 | 0.132479 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110855 | GTCTGTATATGCTGC[C/T]ATTGCACCTGACATG | 23072 |
rs78400273 | snp | A/G | 0.189261 | 0.242509 | intron-variant | HECW1 | GRCh38.p7 | 7:43184671 | GATCACCAATGGCCA[A/G]TGATTTAACCAATCA | 23072 |
rs78404575 | snp | A/G | 0.00220208 | 0.0331087 | synonymous-codon, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509104 | CATGTCCGCATTTGT[A/G]GAAAACCATCTTGAG | 23072 |
rs78405814 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HECW1 | GRCh38.p7 | 7:43317388 | CAGCAGGTCCCAGGG[C/T]AGCCCTTGCGAGTGA | 23072 |
rs78405857 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43235760 | CTGGCATCTTGGTGG[-/G]GAGTCCTGAGTGTGG | 23072 |
rs78413089 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | HECW1 | GRCh38.p7 | 7:43235910 | AAATTAATGAAGTGC[C/T]GGGCACGGTGGTTCA | 23072 |
rs78439036 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43361856 | TACATTAAAAAAAAA[A/C]CAGGCCAGGCGCAGT | 23072 |
rs78440952 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43506171 | AACTCTAATCTAATA[C/T]AAACTCCTAAATGCT | 23072 |
rs78460402 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142005 | ATTCCTCCCGAAAAC[A/C]TGCACACGCTGTGCT | 23072 |
rs78465147 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187343 | CCTTTCAAGTGGAGG[A/G]AATTGGGCTCCACCT | 23072 |
rs78472786 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562993 | TTTTAAAACTTTGAT[A/T]TTTTTTTTTCACATT | 23072 |
rs78474990 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43309633 | GCAAATATATCCTAC[C/T]CAATCGTAAACCTTA | 23072 |
rs78477123 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358934 | GGTTCCAGCAATTCT[-/CCT]GCTTCAGCCTTCCGA | 23072 |
rs78482646 | snp | A/G | 0.220843 | 0.248294 | intron-variant | HECW1 | GRCh38.p7 | 7:43434889 | AATAAAGGTGATTAC[A/G]TTTTTCCTTGTGAAA | 23072 |
rs78484705 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43526198 | ATAGATCTTGTGTGG[C/G]ATGGCAACTTGATGT | 23072 |
rs78506878 | snp | A/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43385219 | CCCTCCCCTCTCCCC[A/T]CCCCTCCCCTCTCCC | 23072 |
rs78512109 | snp | A/G | 0.59375 | 0.121031 | intron-variant | HECW1 | GRCh38.p7 | 7:43383105 | GTCCCTGCAAAGGAC[A/G]TGATCTCATTCCTTT | 23072 |
rs78512367 | snp | G/T | 0.0970103 | 0.197722 | intron-variant | HECW1 | GRCh38.p7 | 7:43168674 | CCAAAATAATAATAA[G/T]AATAATAATAATAGT | 23072 |
rs78512374 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43273165 | CAGACACTGGGGACT[A/G]CCAGAACAGGGAGGG | 23072 |
rs78513574 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43330601 | TCAAGGATGTCATCA[A/G]TATGACCTGCTGAGC | 23072 |
rs78516028 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43436167 | AGACTTTGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 23072 |
rs78521560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43181719 | GTTTGAGTTCCTAAT[A/G]TATTCTGGATATTAA | 23072 |
rs78525106 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43540169 | ATCTTTATAGCAGCT[A/C]TAGAGTAGGAAACCC | 23072 |
rs78531406 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43288049 | GAGGAAAGCAACCCA[C/T]CAGCACTCATTGTTA | 23072 |
rs78543772 | snp | A/G | 0.17138 | 0.237316 | intron-variant | HECW1 | GRCh38.p7 | 7:43329762 | ACAGAGATGGGAAAG[A/G]AACAAGCAACTGCTG | 23072 |
rs78552334 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301876 | GTGGAAACTCTGTCA[A/C]AAAAAAAAAAAAAAG | 23072 |
rs78569267 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43151109 | AGCCCTGACTGCAGA[C/G]ATGGTCCCGTGGTCC | 23072 |
rs78569613 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149018 | CATAGAAGAAATTAA[A/G]GAAATACAAAATTAC | 23072 |
rs78572372 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | HECW1 | GRCh38.p7 | 7:43368229 | ACAGAGCACTATTCC[A/G]TGCCTCTGGAGGTGG | 23072 |
rs78576626 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43224186 | AAAATGAATGAATAG[A/T]TGTATTTGCTATTCC | 23072 |
rs78577317 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HECW1 | GRCh38.p7 | 7:43442099 | CCATGTGATCACAGG[A/G]TAAACAAGTGATACT | 23072 |
rs78581037 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43332498 | GCAGGCAAGAATATG[C/G]GGCAGACAAGGGACA | 23072 |
rs78587343 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43314818 | GTAGCTTATCTTCCA[C/T]ATTTTCCGTGCTTTG | 23072 |
rs78617130 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136172 | CTCTATGTGGGTTCT[G/T]CCTGAATCAGAGGCG | 23072 |
rs78618025 | snp | A/T | 0.0905309 | 0.192535 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120139 | ATAGCCCTGTTCAGG[A/T]TGAAACCCAAACTCC | 23072 |
rs78620518 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43222084 | AAGGTTTAAAAGTTC[C/T]TCTAGGCCAGCGTTC | 23072 |
rs78650516 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260931 | CTATTCTAAGAAAGT[A/T]TGCAAACATTAACCT | 23072 |
rs78673053 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | HECW1 | GRCh38.p7 | 7:43222356 | TATTTTGCACATCTT[C/T]CAAAGATTATGCAAA | 23072 |
rs78679094 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43351300 | ACTCCATAGGGGTCC[A/T]TGGCTTTGGTTGTTC | 23072 |
rs78727338 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426982 | TCTACTATCTCTTTT[G/T]ATTAATCTGATGCCT | 23072 |
rs78728195 | in-del | -/TGTTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43389641 | TGTTGTTGTTGTTGT[-/TGTTGT]CGTTGTTTTAAAGAG | 23072 |
rs78732589 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43331959 | GATCCAGAGAACAGT[C/T]ATGGGACAGGACTTT | 23072 |
rs78736800 | in-del | -/TCA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43203236 | TTATCTTTATCATCA[-/TCA]GTTGTGATAGCTGCA | 23072 |
rs78745701 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | HECW1 | GRCh38.p7 | 7:43217701 | GGCATCACTCCTCTT[C/T]TCTTTCTGAACTGTA | 23072 |
rs78771098 | snp | A/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514744 | TTAAGCTAAATAATG[A/T]AGGATCCATTGAGAA | 23072 |
rs78771173 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | HECW1 | GRCh38.p7 | 7:43202218 | TGAACACAGAGTCTT[C/G]TACTAGAGTCTGCAC | 23072 |
rs78771848 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150808 | TGACACCTGCCACAT[C/T]CTTGGCTCAGAACAG | 23072 |
rs78782003 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43390566 | AAAAAAAAACAGCAG[A/G]GTTGTGGAGGCAGAA | 23072 |
rs78785508 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43453026 | CCCAGATCATGCAGG[G/T]CCTTGTAAACCATTT | 23072 |
rs78799161 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43242874 | GAGAAGTCCAGTAGC[A/G]TCCACCAGGGCGTTG | 23072 |
rs78830237 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43446854 | CCTGTGAGTAGAAGG[G/T]AATGGGAAATGCCTT | 23072 |
rs78840311 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43360674 | ACTTAACTTGGATAC[A/G]AAAATGTTAAGGCCA | 23072 |
rs78841544 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520418 | TCCCGGGCAGCTCCT[C/T]CTCTGCCCTCCCCAC | 23072 |
rs78850547 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121746 | ATTTATCTCCCTACA[A/G]AATTCTCCTGGAATG | 23072 |
rs78862114 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43312993 | CAGACACACAACACC[A/G]GATTTAACATCACAG | 23072 |
rs78882705 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43422382 | TGTTTTTTTTTTTTT[G/T]TGAGGAGTCTCGCTC | 23072 |
rs78886524 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150042 | TTCTTGCAGTGCAAT[A/G]TATCTTATGGTTAAA | 23072 |
rs78893787 | snp | A/G/T | 0.0414688 | 0.138067 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248259 | CACCCCTCTCCTGAC[A/G/T]CAGAATGGGCATTGT | 23072 |
rs78895124 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | HECW1 | GRCh38.p7 | 7:43274893 | ATGAAAAGTACTGTC[A/G]TTTTGCCTATCATAT | 23072 |
rs78896906 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | HECW1 | GRCh38.p7 | 7:43279008 | TAGTCCCTGGCTTAC[A/G]GGAAGTCAGTTGCAT | 23072 |
rs78901211 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43208037 | CTTTATATCTGGAAA[C/T]TTCACCATCATCCCT | 23072 |
rs78902925 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43170328 | GCACAATAAATGTAA[A/T]GTTCTTGAATCATCT | 23072 |
rs78905003 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141584 | AGCTCACCGCGCCTC[C/T]GCCTCCTGGGTTCAA | 23072 |
rs78916460 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43267604 | AAATATAAGAAGAAA[C/T]TAATAAACTATAAAC | 23072 |
rs78926718 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43246090 | GATCACTTGACGCCA[C/T]GAGTATGAGACCAGC | 23072 |
rs78933255 | snp | A/C | 0.039522 | 0.134904 | intron-variant | HECW1 | GRCh38.p7 | 7:43226080 | GGCCAGTTGAATAGA[A/C]CTTTGATTTGGATTT | 23072 |
rs78940571 | snp | C/T | 0.192401 | 0.243274 | intron-variant | HECW1 | GRCh38.p7 | 7:43390364 | GGCAACATAGTGAGA[C/T]CCCGTTCCTACAAAA | 23072 |
rs78981700 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | HECW1 | GRCh38.p7 | 7:43335787 | CTTTCTTCCTTTCTT[C/T]CTTCCTTCCTTCCAT | 23072 |
rs78990837 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | HECW1 | GRCh38.p7 | 7:43504512 | CTCCCCTGGCCCTCT[A/C]CGTTTTGTTTCTACC | 23072 |
rs78997177 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43272047 | AAATAAGGCCACCCC[C/T]CTACAGTCATGTAAT | 23072 |
rs78998945 | snp | C/T | 0.300421 | 0.244863 | intron-variant | HECW1 | GRCh38.p7 | 7:43361578 | CACTTCTTTTGTTCC[C/T]TGCTGTGTGGCTTTG | 23072 |
rs79018008 | snp | A/G | 0.222928 | 0.24853 | intron-variant | HECW1 | GRCh38.p7 | 7:43212208 | AAGGCTATTAAATGA[A/G]ATGCATGAATAAAAC | 23072 |
rs79019828 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43240604 | TAAATATTTGCCCAG[A/G]AGAAACATCCTGCTT | 23072 |
rs79020365 | snp | A/G | 0.416871 | 0.186156 | intron-variant | HECW1 | GRCh38.p7 | 7:43430813 | TTGAGATGGAGTCTC[A/G]CTCTGTCCCCCAGGC | 23072 |
rs79039015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43457077 | TTGAAAAACTAGGCC[C/T]TCTCTATTGAAATTG | 23072 |
rs79039939 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43361817 | AAAAAGACTCTCTCT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs79045522 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43534259 | CCCCTTCCATAAATC[A/G]TGGCCTGTAAATAAG | 23072 |
rs79055107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351425 | GCGATGCCTTAGAAC[A/T]CTCAAGATTATATGC | 23072 |
rs79063661 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135317 | GACTCATCTGACATG[C/T]CTCATTCACCTCTTA | 23072 |
rs79066439 | snp | G/T | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43309308 | GGTGGTGGGAGAGGG[G/T]GGGGTGCAAGGGACG | 23072 |
rs79075772 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | HECW1 | GRCh38.p7 | 7:43357045 | ACCACAATGAGTTAT[C/T]ATTCACCCCAATTAA | 23072 |
rs79076568 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43259388 | TGAGACTCCATGTCC[A/C]AAAAAAAAAACCGTT | 23072 |
rs79079173 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43173860 | GATTTTTTTTTTTTT[G/T]GGAGACAGGGTATCA | 23072 |
rs79080165 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43460683 | ATGGAGGAGGATATT[A/G]ATGGATAATTCCTAA | 23072 |
rs79081406 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43480449 | GACATTTCCCAAGTA[C/T]CTGTGCCTTCTTTTT | 23072 |
rs79089209 | snp | A/C | 0.0327778 | 0.123752 | intron-variant | HECW1 | GRCh38.p7 | 7:43422321 | AGGGTTGGGCCTGAA[A/C]TTTTAGAGTATACTT | 23072 |
rs79093448 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360228 | TTCTTTTTTTTTTTT[-/TTT]AAATGGAGTCTCACC | 23072 |
rs79095804 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43465376 | TCGTGGGTCAGCTGC[A/G]GAGTCGGCCACAGGC | 23072 |
rs79096823 | snp | A/G | 0.194902 | 0.243853 | intron-variant | HECW1 | GRCh38.p7 | 7:43493393 | ATCAGATTACATATC[A/G]TTTATATGGTACTGA | 23072 |
rs79096985 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | HECW1 | GRCh38.p7 | 7:43498972 | CAGTATTTTGGAAAA[C/T]AGATTTTTTTTTTCA | 23072 |
rs79112162 | in-del | -/AAA | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299265 | ACACTGTTGAGCAAA[-/AAA]GATTCCACGAGGCCG | 23072 |
rs79117591 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43292152 | TCAAAATAAACAGCT[C/T]GAAATAATCCTTATG | 23072 |
rs79140880 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43526831 | CATAGCAAGACCTGT[A/C]TCTACAAAAAATAAA | 23072 |
rs79147429 | snp | C/G | 0.0991586 | 0.199366 | intron-variant | HECW1 | GRCh38.p7 | 7:43310528 | TCCAAACAGGAGACA[C/G]AGATGAGTGAAAGGG | 23072 |
rs79149104 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43468538 | CACTTTTTTTTTTTT[G/T]GGAGACAAGGCCTTG | 23072 |
rs79149547 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | HECW1 | GRCh38.p7 | 7:43218785 | ATAGAGAAAGTGATA[C/T]AACGAGTGGAGGAAC | 23072 |
rs79179784 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43241527 | AAAGTGAAATACACC[A/G]GTATCCCCAGTACTA | 23072 |
rs79180793 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523466 | AAAAAGTGGATGGAA[C/G]AAGAGCCCAGAGGAG | 23072 |
rs79185801 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125926 | CAGTCTAAGCTCAAG[A/G]AGACCTTGCTTTCTA | 23072 |
rs79185941 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151810 | AATTGGAACAGATGG[A/G]GAAGGGATAATATTT | 23072 |
rs79187394 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154688 | GAAAGCCCTGTATTC[C/T]AGCACAGGAAGCAGG | 23072 |
rs79191855 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43391755 | TATAATGAGGGTCTA[A/C]TGAGGGAAATGCACT | 23072 |
rs79193863 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43450058 | TTCTAAACTTTCTCC[A/C]TGTTTGTCTTTCTTC | 23072 |
rs79209356 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43166783 | GGAAAGGGCCCATTT[A/G]AATTATTGATCTTAA | 23072 |
rs79212060 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518827 | ATATCACCTTATAAC[A/G]ATCAAATTGCCAAAA | 23072 |
rs79221718 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | HECW1 | GRCh38.p7 | 7:43472194 | AACAGCCTCTAAAGC[A/G]GAAGGAAGGAACCAG | 23072 |
rs79228152 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43457211 | AGCATTGTCTCTGAC[A/G]TCTTGCTCTTTAAGA | 23072 |
rs79231191 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43347568 | CCATTCTCACCACTC[A/G]TCTTCAACATGGTCC | 23072 |
rs79236387 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363345 | GTTCAGCAGGTGCCT[A/G]ATTGCTACTGCCCTG | 23072 |
rs79243585 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43225802 | AGATCTTTTTTTTTT[G/T]GGGACAGGGTCTCAC | 23072 |
rs79246505 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43384539 | AGCAAGAAAAAAATA[C/T]GTCTTTGCCTAAAAC | 23072 |
rs79246905 | snp | C/T | 0.264632 | 0.249571 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124528 | TGTGAGCACACATCT[C/T]CCAGGACCACAGAAC | 23072 |
rs79247391 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376867 | CAAGGACTCTGTCTC[A/C]AAAAAAAAAGACATT | 23072 |
rs79250198 | snp | A/G | 0.119281 | 0.213102 | intron-variant | HECW1 | GRCh38.p7 | 7:43532562 | CCCTTCTCTCTCTGG[A/G]GTCCACCCCCACTGG | 23072 |
rs79253490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43385095 | AAAGATCCTGAATTC[A/G]AAGAAACGGGTTCAG | 23072 |
rs79260041 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293555 | GGCATGAAACAACCT[A/T]AGGTTCCCTGTCTCC | 23072 |
rs79274887 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43545150 | CATATGCATAGAATC[A/T]CCCTGGAAGGGAAGT | 23072 |
rs79278746 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118241 | TGAAAGAAAAAAAAA[A/G]GATCAAAATTCACAT | 23072 |
rs79307354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43169248 | AGATCCGGAAGTTCA[A/G]GAAATACCTGTATGG | 23072 |
rs79331495 | snp | G/T | 0.0733688 | 0.176922 | intron-variant | HECW1 | GRCh38.p7 | 7:43237384 | CAGCTCATCTGTTCG[G/T]TGTGTCTCCCCTCCT | 23072 |
rs79342263 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126595 | AAGTATACAGGTATA[C/T]CTTGTTTTATTGCAT | 23072 |
rs79357748 | in-del | -/TAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315493 | TATTATTATTATTAT[-/TAT]CATTATTACTATTAT | 23072 |
rs79382842 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43165744 | TTGTGAAAATATGCT[A/G]TAAGCTTTATATTAA | 23072 |
rs79413573 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HECW1 | GRCh38.p7 | 7:43432930 | TAAATGGCCTATTGA[A/G]TAAACAACACAAACA | 23072 |
rs79414187 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43457774 | AGTAAGACTCCATCT[A/C]AAAAAAAAAAAAACA | 23072 |
rs79420065 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43249803 | GCTTGGTAGTGCTAG[A/T]TTTAGAGCTCAAAAT | 23072 |
rs79420769 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300663 | ATATCAGATATGGCC[A/G]TGTTCATCCGGGGCA | 23072 |
rs79422582 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529116 | AACCTCATTATCACC[C/T]AGAACTGTGCCATGT | 23072 |
rs79423825 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43418318 | ACAATTCAACTCATA[A/T]CAGTTTTCCTCTAAT | 23072 |
rs79426405 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43320920 | GTGAGGTCTAGGGCA[A/G/T]TTGGATAAAAGCCAG | 23072 |
rs79427113 | snp | C/G | 0.188631 | 0.242351 | intron-variant | HECW1 | GRCh38.p7 | 7:43393493 | AAACATTTTTACTTC[C/G]TGGAAAATGTTTATT | 23072 |
rs79430182 | snp | A/G | 0.201418 | 0.245234 | intron-variant | HECW1 | GRCh38.p7 | 7:43350307 | AAGATTCTTTCCTTC[A/G]TCTTAACTTTAGATA | 23072 |
rs79447357 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43178684 | AAAGGTGAGAAAGTG[A/G]AGGCTGAAAGATGGA | 23072 |
rs79451421 | snp | C/T | 0.0168055 | 0.0901129 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563949 | TTGCAGCGATGTGTC[C/T]GTTGTCAATCAAGGA | 23072 |
rs79458965 | snp | A/C | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43546630 | TCAAAAAAAAAAAAA[A/C]AAACAAACTTTAAAA | 23072 |
rs79472827 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | HECW1 | GRCh38.p7 | 7:43532969 | AAAGGCAAGTTAGAA[A/G]GGAGTATATCATCAC | 23072 |
rs79492572 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43561554 | ACCATAGAGTTTATA[A/G]TCAGTTTGCTAGTGT | 23072 |
rs79495743 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | HECW1 | GRCh38.p7 | 7:43271680 | GAGAACTACAAAACA[C/T]TGATAAAATAAATCA | 23072 |
rs79505142 | snp | G/T | 0.115788 | 0.21092 | intron-variant | HECW1 | GRCh38.p7 | 7:43530269 | GGCTCATGCTTTACT[G/T]TAATCGACACTTTAC | 23072 |
rs79505317 | snp | A/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297903 | ATAGAGAGACCTGTC[A/T]CTAGAAAAACATTTT | 23072 |
rs79507150 | snp | A/T | 0.0379877 | 0.132479 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110856 | TCTGTATATGCTGCC[A/T]TTGCACCTGACATGT | 23072 |
rs79515881 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524438 | CTTATTACTTAAATA[A/C]TGAGGTTGAGAAAGG | 23072 |
rs79518835 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43323852 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 23072 |
rs79521723 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43397295 | GCTCAAAAATGCTCA[G/T]TCATGGAAAAAAAAT | 23072 |
rs79523592 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299880 | ATTGTTCCTTTCTTT[C/T]ACCATTCCCCTGAAT | 23072 |
rs79527650 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | HECW1 | GRCh38.p7 | 7:43292211 | TTCTGGTCTCCTACA[A/G]TCATATCTTAGGATA | 23072 |
rs79529244 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43364738 | AATATAGGACTTATT[A/G]TCCCTATATATCTTC | 23072 |
rs79529987 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | HECW1 | GRCh38.p7 | 7:43310692 | ATTGATCTAACTGAA[A/G]GAGTAGACTATTGCT | 23072 |
rs79542022 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43421278 | AGTCTCACAACATAC[A/G]CAGTCTATTCCAAAT | 23072 |
rs79544762 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43393678 | TCTTTTTTCTTCTTC[C/T]TTTTTTTTTTTCATC | 23072 |
rs79547591 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | HECW1 | GRCh38.p7 | 7:43164085 | GCCCAGGCTTGGGTG[A/G]AGGTAGTGGGAATGA | 23072 |
rs79549004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43281972 | CCATGAGCCTTTTTC[A/G]AGTCCCTCATCCAGC | 23072 |
rs79549908 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43383027 | ATGAGTGAGAACATG[C/T]GGCATTTGGTTTTCT | 23072 |
rs79562993 | in-del | -/G | 0.3742 | 0.216966 | intron-variant | HECW1 | GRCh38.p7 | 7:43180063 | TTCACAACTGCACTT[-/G]GCCAGTTTACGTTAT | 23072 |
rs79570651 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | HECW1 | GRCh38.p7 | 7:43239225 | CATCCCACCTCTTGG[A/G]CTCTTGCAACAAAGA | 23072 |
rs79579647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43200392 | GAAAATTTTGGCTCA[G/T]GCATGTCACTCAATT | 23072 |
rs79586318 | snp | G/T | 0.143959 | 0.226396 | intron-variant | HECW1 | GRCh38.p7 | 7:43371614 | CAAAATTTATCAAAT[G/T]TATCAAAATTTATCT | 23072 |
rs79586558 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506979 | GGAGGCTGAAGTAGC[A/C]GAATCGCTTGAACCC | 23072 |
rs79589046 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43456007 | CTCTGTCTCAAAAAG[A/G]AAAAAAAAAAGAAAG | 23072 |
rs79589337 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43550945 | ACAAAAATAAGTGAA[C/G]TGAAGACATTGGGGG | 23072 |
rs79600122 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118924 | CACATCCCCCATGAT[G/T]GATTTTCTGTTTCTT | 23072 |
rs79600800 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160255 | TTATACATATTTTCA[A/G]TATTTCCCCCCAATT | 23072 |
rs79612891 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43478179 | CCCAGCACTTTGGGA[A/G]GGCGAGGTGGGCAGA | 23072 |
rs79613988 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | HECW1 | GRCh38.p7 | 7:43266252 | AGCTACCTCATTACC[A/G]TAAACTCTGGTAGGG | 23072 |
rs79625512 | snp | G/T | 0.040671 | 0.13668 | intron-variant | HECW1 | GRCh38.p7 | 7:43215547 | TAACAAATGGTTAAG[G/T]TATTTTTAAACTTCA | 23072 |
rs79626764 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43173573 | CATTAGTTAGATTCT[C/T]ATAAGGAGCATGCAA | 23072 |
rs79646663 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130865 | AGAAATGCTCAACCT[G/T]TATTAATAACTGGGT | 23072 |
rs79650638 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43373207 | GCCTTCTTCCTTTTT[C/T]TTTTTTTTTTTTTTC | 23072 |
rs79652535 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43504009 | TGGGGCCCAGGTAGG[C/T]GGGGCCCCAACGCTT | 23072 |
rs79654928 | snp | G/T | 0.5 | 0 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298342 | TTCTATTTCAGTTCA[G/T]TTTCCAGGGTTTGGC | 23072 |
rs79655368 | snp | A/G | 0.0150222 | 0.0853548 | intron-variant | HECW1 | GRCh38.p7 | 7:43554586 | CCCTCCCTTTGCCTC[A/G]TGCAGGTTACCACGA | 23072 |
rs79660011 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43366103 | GCAAGACTGTCTCAC[A/C]AAAAAAAAAAAGAAC | 23072 |
rs79677697 | snp | A/T | 0.188316 | 0.242271 | intron-variant | HECW1 | GRCh38.p7 | 7:43502503 | CTCTACCAAAAAAAA[A/T]TTTTTTTAATTAGCC | 23072 |
rs79687994 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43301103 | AGGTGAACAAAACCT[C/G]CGTGGCCCCCCACTC | 23072 |
rs79713729 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43527877 | ACAGAGAAACCAGTG[A/G]AAAAAATTTCAACTG | 23072 |
rs79714205 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43504160 | CAAGCAGGTCCTTCC[A/G]TCCTCCTGGATGACT | 23072 |
rs79740466 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296795 | CAGGGTGCACTTTGC[A/G]GCCTCCACAGCTCTG | 23072 |
rs79741628 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | HECW1 | GRCh38.p7 | 7:43260424 | CACAGGGAGCAAGGA[A/G]AAGAGATGAGCCACA | 23072 |
rs79743601 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43222233 | AATCACAAGGAAATA[A/G]CCTGGATCCATTCAG | 23072 |
rs79772140 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43204126 | CTTATACCTTGGCAC[A/C]ATAATAAATAAATAT | 23072 |
rs79776216 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506974 | ACTCGGGAGGCTGAA[A/G]TAGCAGAATCGCTTG | 23072 |
rs79780892 | snp | A/C | 0.030665 | 0.119967 | intron-variant | HECW1 | GRCh38.p7 | 7:43542755 | TGGGATTTTGTTTTT[A/C]AATTAGCGAATAAGG | 23072 |
rs79782158 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519987 | CCAGCCATGCCAGGA[A/G]AAGCCAAAGTCTATA | 23072 |
rs79792045 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43352185 | TCCACTGCCTTGCTA[A/G]GTCTCTGATGCCTTC | 23072 |
rs79802120 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162583 | GCACCCTTTTCCCAG[A/T]TAAGGTCATATTCAC | 23072 |
rs79808592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43394526 | ATCCATCTCCTTGAG[C/T]AACTAAAATTGGGGT | 23072 |
rs79809559 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43330562 | TCAAGAGCAAGGCCC[G/T]GGAAGTCAAGGGAGG | 23072 |
rs79819354 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43453318 | CTGGACATATATTTT[A/T]AAGGTAGATTTGATG | 23072 |
rs79820352 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43480168 | AATGTATCCATGGAC[G/T]AGAAACTAGGGGGAA | 23072 |
rs79824824 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | HECW1 | GRCh38.p7 | 7:43422692 | ATACTTCTTGATGCC[A/G]AGTGCTTTACCAGAA | 23072 |
rs79842123 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43561038 | GCTAGTCAGGTGATT[C/G]AAGGCTCCACAGCAG | 23072 |
rs79869935 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136604 | TGGCAGTGTATGGCT[A/G]TGGCCTCAGCCTCAT | 23072 |
rs79873609 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43428232 | TTCTGCCAGAACAAT[A/G]ACTGGTGTGAGTTGG | 23072 |
rs79874322 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43494330 | CTTCTCCCTGCCATG[G/T]TTCAAGTTTAGGTGC | 23072 |
rs79886968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43261206 | AGAGAAGTTATGGCT[A/G]GTGATGAATATTTGA | 23072 |
rs79904083 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43307294 | GCTGATATTCTTGTG[A/G]TCCTCCTATCAGTTC | 23072 |
rs79913089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43493986 | CTAGAATCCCATCAA[C/T]GGCTGCATTTCATTA | 23072 |
rs79919326 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360230 | CTTTTTTTTTTTTTT[A/T]AAATGGAGTCTCACC | 23072 |
rs79924158 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43225234 | TATTTTACAACCATC[A/G]AGTTAAAAACAAAGA | 23072 |
rs79929953 | snp | C/G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113673 | TGCCGGGGCGGGGAG[C/G/T]GGGGGGGAATGCGTC | 23072 |
rs79935257 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43339327 | ACCTTCTTTCAATCC[A/G]GATATTTTCAGTCGA | 23072 |
rs79938704 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43294087 | ATGAAATCGATCCCT[C/T]GTGCCAAAAAGTTTG | 23072 |
rs79970441 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | HECW1 | GRCh38.p7 | 7:43492464 | TCTATTCAGTGATTT[A/G]TTAATCCCGTGCACA | 23072 |
rs79974567 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134946 | TTTTGCTAAAATGTC[G/T]AGGTATATAGGTTTT | 23072 |
rs79974968 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43546243 | TTTTTTTTTTTTTTT[G/T]CCATATCCACAGTCT | 23072 |
rs79984672 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43253910 | TGAAATTCCGTCTCA[A/C/G]AAAAAAAAAAAGACA | 23072 |
rs79985588 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | HECW1 | GRCh38.p7 | 7:43433491 | GGCTAAGACCCACTG[A/G]TCAAAGCAAAAGTAA | 23072 |
rs79989657 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43277183 | AAACCTCCCTTATCT[C/T]CTCTCCATCCTCCTA | 23072 |
rs80005975 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43425456 | AAGTCTAATTTTATA[G/T]TCAGCTTACCTCTCT | 23072 |
rs80025311 | snp | A/G | 0.130008 | 0.219321 | intron-variant | HECW1 | GRCh38.p7 | 7:43244935 | TTGGTACGCGTCAGC[A/G]GGCGGGAAGATGAGG | 23072 |
rs80033234 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | HECW1 | GRCh38.p7 | 7:43216976 | TAATCTTAAAGCATC[C/T]TTGCACCAGAGGGAC | 23072 |
rs80050633 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43373206 | TGCCTTCTTCCTTTT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs80059351 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | HECW1 | GRCh38.p7 | 7:43542614 | ACCTGGGTTTTTCCA[C/T]CTTTTGGCTATTGTG | 23072 |
rs80064485 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43322770 | TTAGACATAATACTC[A/G]AATGTGTGCACAAAC | 23072 |
rs80071700 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43189395 | GGTCCACAGATTACA[A/C]AGTGAATAGCAAAAT | 23072 |
rs80077495 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43560903 | AACACACCACCCTTA[A/G]GGAGGAAAAGGCAGG | 23072 |
rs80087535 | snp | C/T | 0.382666 | 0.211895 | intron-variant | HECW1 | GRCh38.p7 | 7:43334039 | TTTCCACTTTATTCC[C/T]ACGTTATACCTCTCT | 23072 |
rs80096274 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | HECW1 | GRCh38.p7 | 7:43232183 | CTGGTTGATTGGGAT[A/G]GTTTGAATGGGCCAC | 23072 |
rs80103686 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | HECW1 | GRCh38.p7 | 7:43327261 | AAAAAGTATGACTCC[A/G]TATACATATCTGCAA | 23072 |
rs80104819 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148616 | GGGTCTGAGTCCAAA[A/G]CCTGTACTCTTTGGA | 23072 |
rs80108818 | snp | A/G | 0.209693 | 0.246729 | intron-variant | HECW1 | GRCh38.p7 | 7:43409051 | ATTTAGAGCTTTCAA[A/G]CATCCTTGACAAGAA | 23072 |
rs80160500 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43410769 | TCAAGAAATATTGCC[A/G]TCTTTTTGTGTTGTT | 23072 |
rs80167854 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | HECW1 | GRCh38.p7 | 7:43553028 | TGTCTCATTTCCTAC[A/G]GAATTGGAGCCCTCT | 23072 |
rs80172463 | snp | A/T | 0.0381859 | 0.132796 | intron-variant | HECW1 | GRCh38.p7 | 7:43434042 | ATACATCCTTTTTTT[A/T]AAAAAAAAACAAAAA | 23072 |
rs80172675 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | HECW1 | GRCh38.p7 | 7:43469221 | TGAGAGATGTGCTAT[C/T]GGCCGCCAGCAGTAA | 23072 |
rs80197238 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43304008 | GAAGGCAATTCCCAG[A/T]GAGGTGGAGCCCTTC | 23072 |
rs80205527 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43195186 | ACATATTGCTAATTC[C/T]ATTTATTTCCCAAGA | 23072 |
rs80212680 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43370696 | GAGCTGCCAAGCTAT[A/G]AAAAGACATGAGGAA | 23072 |
rs80214812 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43534840 | CAATCCACGTTTTCA[C/T]TCTTCAATTCAGAAT | 23072 |
rs80226972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43406475 | CAACTGTGCTTTTTC[A/G]TCAGTAACAAATTAT | 23072 |
rs80233237 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426979 | ATCTCTACTATCTCT[C/T]TTTATTAATCTGATG | 23072 |
rs80236433 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | HECW1 | GRCh38.p7 | 7:43241942 | GGAAGAAGGGCTGAC[A/G]GCAGCTCAGGTCAGG | 23072 |
rs80250932 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | HECW1 | GRCh38.p7 | 7:43233775 | AGTCAGTCTCAAAGC[C/T]TCCACTTGCTCCTCT | 23072 |
rs80260826 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43320196 | GAGGAGAGATGATTC[C/G]AAGTGGAGTCCGTGA | 23072 |
rs80265753 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513943 | CTCAAGGACACAGCC[C/T]CTGCGAGACCTGGCC | 23072 |
rs80279419 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269704 | CTAGAGCCTTTTTAA[C/T]TGTTGTCAAAAGTCT | 23072 |
rs80286615 | snp | A/G | 0.226779 | 0.248919 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149694 | TTTTGCAACTTTTCT[A/G]TAAGCCTAAAATTAT | 23072 |
rs80294570 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HECW1 | GRCh38.p7 | 7:43447828 | AAATTCCTTTACTGT[A/G]GAAACTGCATTAGAC | 23072 |
rs80331923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43235356 | CAGGAAAAGTGTTTA[A/G]AGATAATACTTGGGA | 23072 |
rs80351477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43496260 | ATGCTGATGGAAGCA[C/T]TTATGGACTCTCCTC | 23072 |
rs111069919 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247941 | AGGAAAAAAGAGAGA[A/G]AAAAAAGGAGGGAAG | 23072 |
rs111069920 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247977 | AAAAAGAGAAAGGAA[A/G]GAAGGAAGGAAGAAG | 23072 |
rs111162282 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247907 | GAGAGGAAGGAAGGA[A/G]GGAGGGAGGAAGGGA | 23072 |
rs111163408 | snp | A/G | 0.170733 | 0.237101 | intron-variant | HECW1 | GRCh38.p7 | 7:43198508 | ACACTCAAACACCAT[A/G]GTCACACACCACAGA | 23072 |
rs111211420 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247809 | GAAGGAGGGAAGGAA[A/G]GAAAAGAAAGAGAGA | 23072 |
rs111211421 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247821 | GAAAGAAAAGAAAGA[A/G]AGAGAAAGGTAAGAA | 23072 |
rs111211422 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247935 | GGAAAGAGGAAAAAA[A/G]AGAGAGAAAAAAGGA | 23072 |
rs111227376 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43497471 | TTTAGTGACCACAGA[A/T]GCAATCATATTTCAT | 23072 |
rs111228643 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | HECW1 | GRCh38.p7 | 7:43349057 | TTTGTTTTTTGAGAC[A/G]GAATTTTGCTCTGGT | 23072 |
rs111233367 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | HECW1 | GRCh38.p7 | 7:43421183 | TGCTGCTGCTGTATG[C/T]TATGGAAAGGATAGC | 23072 |
rs111234394 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43204783 | GTTAATTGACACTTA[C/G]CTGGAGGAGAAACAA | 23072 |
rs111234573 | snp | A/G | 0.079617 | 0.182947 | intron-variant | HECW1 | GRCh38.p7 | 7:43446064 | TTTAGAATTCAACTA[A/G]CCCATGTACGTACAT | 23072 |
rs111240926 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43429331 | ATATATATATATATA[C/T]ATATACATATATGCA | 23072 |
rs111251783 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43185307 | CCTGTATCATCTGCA[A/G]TATCCTTTACAATAA | 23072 |
rs111254619 | snp | A/G | 0.000314869 | 0.0125433 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43466454 | TTTTTCAGATCTAAG[A/G]AGAGAAGGGTCACTT | 23072 |
rs111264194 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514931 | GGTAGGAATAGGAAC[C/T]CAGGTATCATGGCTC | 23072 |
rs111267345 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126582 | TTTATATGAAAACAA[A/G]TATACAGGTATACCT | 23072 |
rs111272355 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43273249 | TGGTTGACAGGAACA[C/T]GTGTACCCCAAACCT | 23072 |
rs111274465 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43539672 | CACCTCTAAGTGCGG[A/G]ACCACGGGCCCATCA | 23072 |
rs111285883 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | HECW1 | GRCh38.p7 | 7:43303978 | CCAACACTTTCTTCT[C/T]ATTTGACAGGTGATG | 23072 |
rs111291776 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43468413 | ACAGCGAGAAAACCA[C/T]GTGGAGTCGCACAGA | 23072 |
rs111292127 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43256332 | AGATGAACATCGGCT[G/T]GGTACGGTGGTTCAC | 23072 |
rs111292967 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43181819 | TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 23072 |
rs111294398 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43278471 | CTCCTGTTCCCACCC[A/G]TGCGGCCCGTTCTCA | 23072 |
rs111294699 | snp | C/T | 0.355311 | 0.226737 | intron-variant | HECW1 | GRCh38.p7 | 7:43262120 | CAGCTACTTGGGAGG[C/T]TGAGGCATGAGAATT | 23072 |
rs111302637 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43476028 | CACTTCTTATTTAAC[A/G]TTGTTCTAGAAGTAC | 23072 |
rs111311899 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43181801 | TGTTTGTTTGTTTTT[G/T]TTTTGAGATGGAGTC | 23072 |
rs111312466 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43234780 | CAGGGCCTGTAGGCT[G/T]TGTTGCTCACTCACG | 23072 |
rs111313146 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43267910 | AACTATAAAACTTGC[C/T]AGATAATTTTTAATG | 23072 |
rs111320466 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43282233 | AACCCAGTTCAGTGG[C/G]TGGTGCATCACTTTA | 23072 |
rs111321716 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520928 | CATCTTATTGTTCAG[C/G]TTTGCCCTCTGCAGC | 23072 |
rs111328129 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43316681 | AACAGCCTCCTGGTA[A/G]AGAGCCTAGAGCACC | 23072 |
rs111333027 | in-del | -/GT/GTGTGTGT | 0.455621 | 0.142197 | intron-variant | HECW1 | GRCh38.p7 | 7:43210450 | ATCAAGTAGAAGTGA[-/GT/GTGTGTGT]GTGTGTGTGTGTGTG | 23072 |
rs111333403 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143173 | ACGGGGTTTTACCAT[A/G]TTGGCCAGACTGGTC | 23072 |
rs111365106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132174 | TCACAGCGCCCCCCC[C/G]CCCCAAGTAAGGTTT | 23072 |
rs111366637 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43554121 | CCTGGGATCTCCTGT[C/T]CACGAAACTGGCTGT | 23072 |
rs111371091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43264612 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 23072 |
rs111371623 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43307048 | ATAAACAAAACATTG[A/G]TGGCTCTTCTGCTAC | 23072 |
rs111384032 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43348980 | TGAATAGAATGTGTG[A/T]TCTGTGTTTGTTGAA | 23072 |
rs111390474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192132 | ACCCGGCTAATTTTT[A/G]TATTTTTGTAGAGAT | 23072 |
rs111416269 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43346316 | GAATTGTCTATTCAC[A/G]TCCTTAGCCCACTTT | 23072 |
rs111422942 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43177796 | CCTCCCATCTCAATG[C/T]CTTCTCCCCTTCTCT | 23072 |
rs111423084 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134222 | AACATGATGAAACCC[C/T]GTCTCTACTAAAAAT | 23072 |
rs111425350 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43362735 | CAGAGCAGGAAGGCA[C/T]TGAGCACACAACAGG | 23072 |
rs111430984 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43169909 | TGAGGCTGATTGATT[C/T]TGAGCCTCTAGGGTA | 23072 |
rs111435232 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43188672 | TCTGAGGAGTTCAAT[A/G]AAAATTAAATGTACT | 23072 |
rs111444306 | in-del | -/T | 0.26326 | 0.249648 | intron-variant | HECW1 | GRCh38.p7 | 7:43253128 | CTCAAACATCCGCAC[-/T]TTAAAAAAAAAAAAA | 23072 |
rs111452917 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43409234 | CTTCCTCCTAGCGTT[C/G]GTTATCAACAGATTC | 23072 |
rs111475759 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43219580 | TGTGTGAGAGGGTCA[C/T]GATCGATTGAGCAAG | 23072 |
rs111475932 | snp | A/G | 0.186105 | 0.241697 | intron-variant | HECW1 | GRCh38.p7 | 7:43499150 | GCCAAGCCTGGTGGT[A/G]TGCGTTTGTAGTCCC | 23072 |
rs111505937 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43193061 | TGGGAATTCTGGAAC[C/T]GATGGTCCCTCCCCC | 23072 |
rs111508617 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43447647 | AGTCCCCAGGCTAAC[C/T]GTGTCTGCATTGTGG | 23072 |
rs111512025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203086 | GTGGTCTCTTCACAC[A/G]GACGCGCGTGACACT | 23072 |
rs111516430 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150894 | TTTATCAGCGCCCCC[A/C]CACACAGACGGCAGC | 23072 |
rs111523810 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308080 | ATATATAAATATAAT[A/T]TATTATATATTATAT | 23072 |
rs111534874 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43555107 | GAGGGCAGAGGCAAG[A/G]ACATTAATATAAAAA | 23072 |
rs111563665 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211789 | ATAAATCAAGACATC[A/C]TAAACCCTTTGAGCT | 23072 |
rs111573649 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43181810 | GTTTTTGTTTTGAGA[C/T]GGAGTCTCACTCTGT | 23072 |
rs111584624 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133637 | TTTCTCTGTTCCTTC[C/T]TTACTCTGTCCCTTA | 23072 |
rs111600910 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | HECW1 | GRCh38.p7 | 7:43272276 | CTGGACATCAGCCTT[A/C]GGAAAGAATTTATAA | 23072 |
rs111600912 | in-del | -/C | 0.187369 | 0.242028 | intron-variant | HECW1 | GRCh38.p7 | 7:43191485 | GGCCCAGCTGTCACC[-/C]ATGTGTGTGCTTATA | 23072 |
rs111603237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43166960 | ACTTCACCTCTCAGG[C/T]TGTAGGCAGCCACTG | 23072 |
rs111605353 | in-del | -/AACA | 0.65139 | 0.0639445 | intron-variant | HECW1 | GRCh38.p7 | 7:43383827 | AGAAGCCTTGCCAGT[-/AACA]AACAGTTGATTAACA | 23072 |
rs111605563 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129489 | CTACAGTATAGTGTA[A/G]ACATAACTTTTATGT | 23072 |
rs111613346 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43555459 | AAGCACTGAAGAGAC[A/G]GTTGTGCATAGGCGC | 23072 |
rs111615751 | snp | G/T | 0.186105 | 0.241697 | intron-variant | HECW1 | GRCh38.p7 | 7:43499179 | CCAGCTACATGGGGG[G/T]ACTGAGGCAGGAGGA | 23072 |
rs111620965 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43539673 | ACCTCTAAGTGCGGA[A/G]CCACGGGCCCATCAC | 23072 |
rs111627999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43309044 | GGAATTATGCCAGGT[A/G]CAGGGGATATACAGA | 23072 |
rs111634663 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513426 | TGGAGAAACCCCTGA[C/T]AGTGTGTCCTTCCTC | 23072 |
rs111641663 | in-del | -/GG | 0.0333695 | 0.124785 | intron-variant | HECW1 | GRCh38.p7 | 7:43270976 | GGGAAGAAATTGAGA[-/GG]GGTACATCATGTGGC | 23072 |
rs111657198 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43185156 | GGACAGGGATGGTGG[G/T]GGGGAAGGGGCTGGC | 23072 |
rs111667762 | snp | C/G | 0.256061 | 0.249927 | intron-variant | HECW1 | GRCh38.p7 | 7:43263459 | TCCGCCTCCCAGTTT[C/G]AAGCAATTCTCATGC | 23072 |
rs111670473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43391789 | CAGTGCTCTGTAAAC[G/T]TGGGTAAGGTGTGTT | 23072 |
rs111671101 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140535 | TCGTTTCTGGCCTTC[A/G]TGGTCCCTCATTTAT | 23072 |
rs111681562 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302937 | CACACACCCACACAC[A/G]TGCACACACACATGC | 23072 |
rs111692852 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43446068 | GAATTCAACTAGCCC[A/G]TGTACGTACATATAG | 23072 |
rs111702279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160594 | CGCAAAGTCTTCAAC[A/G]TATCAGTGTTTGTTT | 23072 |
rs111703243 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43398232 | ACTGTACTCCAACCT[A/G]AGCAACAGAGTGAGA | 23072 |
rs111705561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43325638 | GTTGTCGTCACTGTC[A/G]TAGGCACCGCCTCCT | 23072 |
rs111706014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43197226 | AAAAAAAAGGAAAAT[C/T]TCTTCTTTTGGGGGT | 23072 |
rs111712157 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43449219 | TTTCTGACACTAAAC[A/T]TGTATACAAACAAAC | 23072 |
rs111716314 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43445649 | AGTTTAAAAACAAGA[-/A]GGGCGGGGGATCGGT | 23072 |
rs111722214 | in-del | -/AT/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214207 | CATTTTTTCAAATAC[-/AT/T]TTTTTTGTTTTTATA | 23072 |
rs111730061 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120734 | CTACAACCTCCGCCT[A/C]CCAGGCTCAAGTGAT | 23072 |
rs111733144 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | HECW1 | GRCh38.p7 | 7:43398128 | CAGGCATGGTGGCGG[C/G]CTCCTGTAGTCCCAG | 23072 |
rs111745935 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180377 | TCTAAGTTTTATTTT[A/T]TTATTTTATTTTTTT | 23072 |
rs111757193 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43428718 | AAAGTTAGAATAATA[A/G]CTCTTTTCTTCCTTC | 23072 |
rs111765657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43451320 | CATTGGATCTGTTAC[A/G]TCACAAGCATCTCCA | 23072 |
rs111765836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244683 | GTGGGTAACTGAGGA[C/G]CATTGATTCCCACTG | 23072 |
rs111767277 | in-del | -/ACACAC | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43345800 | TTCCATCATATATAT[-/ACACAC]ACACACACACACACA | 23072 |
rs111769093 | snp | A/C/G | 0.164108 | 0.239184 | intron-variant | HECW1 | GRCh38.p7 | 7:43382273 | CCTGGGCGACAGAGC[A/C/G]AGACTCCGTCTCAAA | 23072 |
rs111776916 | in-del | -/GT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43480657 | TATGTGTGTGTGTGT[-/GT]ATATATATACACACA | 23072 |
rs111786148 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43212425 | CAAAATATTCTTTTC[A/G]CTTTTTAAAATATAT | 23072 |
rs111794081 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43386231 | TTCAGTCAGCCCCTT[A/T]TAATGTCCCTTTGTT | 23072 |
rs111794084 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43529969 | TTTATTTTTTTTTTG[A/G]GACAGAGTTTCGCTC | 23072 |
rs111801051 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43426576 | TGTTAATAAAATGTC[C/T]TTCATTTCCTTTCTT | 23072 |
rs111803044 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213837 | ACTTTACATCATAAA[C/T]AGCTATAGCATTAGG | 23072 |
rs111812037 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43457495 | AAAACACATGGGGCC[A/G]GGTGCAGTGGCTCAC | 23072 |
rs111813199 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43471312 | AGAGTTAGGAATACA[A/G]CTCACTAAACAGTGG | 23072 |
rs111817111 | in-del | -/A | 0.31014 | 0.242659 | intron-variant | HECW1 | GRCh38.p7 | 7:43404976 | TCCATGTCAAAAAAA[-/A]TCAAACAAAAAAACA | 23072 |
rs111817656 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43168965 | TAAACTGAAATGGTG[A/G]CTTCTGAGAGCTTGG | 23072 |
rs111821262 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43541093 | AAACACATCAAATAA[A/C]AGTGCAAACTAAAAT | 23072 |
rs111825133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43193674 | AGCATGAGCCACCAC[A/T]CCCGGCCACTTGATG | 23072 |
rs111836436 | snp | A/C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43276040 | AGGTTTAAAGAATCA[A/C/G]TTGTGCAGAAGGCCC | 23072 |
rs111838128 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43371139 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 23072 |
rs111838269 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517247 | ATCTAACCTTACAGT[C/T]GTCACAATCAGACAT | 23072 |
rs111841502 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211011 | GGAATGCCTGGGTTT[A/G]TATCCCGGTCATTGT | 23072 |
rs111853872 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43419765 | GCATTTGAATATAAA[C/T]TTAATTTCCCCAGCA | 23072 |
rs111854045 | snp | A/C | 0.5 | 0 | missense | HECW1 | GRCh38.p7 | 7:43445211 | CGTCCTGCTGCAGCC[A/C]CTCGTGCTACAGCTC | 23072 |
rs111858854 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131536 | AAATCATTGACTGCA[-/T]TTTTTTGGTATTTCC | 23072 |
rs111878855 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522536 | CATGGGCTCTTCATG[A/G]AGGCTGGAGGTTAGC | 23072 |
rs111879096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43540250 | AAATTCCACCAGGGA[A/G]GATCTGAGAAAATTC | 23072 |
rs111882544 | snp | A/C/G | 0.339429 | 0.233457 | intron-variant | HECW1 | GRCh38.p7 | 7:43237840 | CAGTCTTTCCCCCCC[A/C/G]CCGCCCCCACTTGGA | 23072 |
rs111885206 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43372193 | CCCATTGATGTAGTT[C/T]TTAATTAATAGTTAG | 23072 |
rs111887773 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43371876 | CCAGGCTAGAGTGCA[A/G]TGGCACGGTCTCGGC | 23072 |
rs111907793 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43404203 | TTTATTCCATGAAAC[A/G]TATATCTCAGTGAGT | 23072 |
rs111915807 | snp | A/G | 0.180702 | 0.240204 | intron-variant | HECW1 | GRCh38.p7 | 7:43447884 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGTGGG | 23072 |
rs111918677 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128456 | GCACATCTGTTTATA[C/G]CATGGTCTACTAAAT | 23072 |
rs111920038 | snp | C/G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43340660 | ATTGGCCCCCTGACA[C/G/T]GTGAAGTAAGTATTT | 23072 |
rs111921566 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43370538 | ACTTATGTCCATACA[A/G]ACATCTTCACATGTT | 23072 |
rs111923020 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43313910 | GTTTAGCACTTGAGG[C/G]AATTAGGTTTAGGCT | 23072 |
rs111948299 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43385265 | CCCTCCCCTCCCCTC[C/T]CCCCTCCCCTCCCCT | 23072 |
rs111998628 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43165683 | CACTCTAATCACTTA[G/T]ATTTTTTTTTAGTAA | 23072 |
rs112000805 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214123 | TTTCTAATTGAAATA[C/T]ACATATGTATTTCTA | 23072 |
rs112005260 | snp | A/G | 0.312104 | 0.242163 | intron-variant | HECW1 | GRCh38.p7 | 7:43488196 | ATGCCTGTAATCCCA[A/G]CTACTCGGGAGGCTA | 23072 |
rs112005474 | snp | A/C | 0.0448719 | 0.142907 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119156 | TTTTGTGTTTCTGCC[A/C]CCTCTCACCTTTTGC | 23072 |
rs112012224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191287 | AGAGTACCCCCAGAC[C/T]AGAAGATACCTGAGG | 23072 |
rs112014125 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43353718 | AAAAGTGAAATGGAG[A/G]TAGACAACCAGCTTC | 23072 |
rs112016119 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136500 | CTCCCAGAAGTTGTA[G/T]AAAGAGACTGCTTAG | 23072 |
rs112022689 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43198040 | ACAACCTACACATAC[A/G]CACACCATAGTCACA | 23072 |
rs112033049 | snp | C/G | 0.0573587 | 0.15934 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150473 | AACCTCTGCTTCCTG[C/G]GTTCAAGTGATTCTT | 23072 |
rs112040128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43185367 | GAGTTCTGTAAGCTC[C/T]TCCAGCAAATTAATC | 23072 |
rs112051194 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43190535 | GAAATACATTGATAC[A/G]GTGGAGCCATGGATT | 23072 |
rs112052569 | in-del | -/AGG | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211972 | CCTGTCTACTATGCA[-/AGG]AGTTCTTAAGGGAGA | 23072 |
rs112057800 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43332096 | GACCATTCTACAGTG[A/C]CCGCTTTCCTAACAA | 23072 |
rs112070451 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130412 | TTATACATGATACAG[C/T]CTGTGTACATTGAAC | 23072 |
rs112079889 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43477633 | TGAATCTGTGTGGCA[G/T]GCTATCTTGGGGAAT | 23072 |
rs112088215 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43483841 | GACGTGAGCCACCAC[A/G]CCCAGCCACAAACTT | 23072 |
rs112090588 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43379981 | ACACAGCAGACGGCC[C/T]ATAAAACATTTGTAT | 23072 |
rs112097930 | snp | A/C/T | 0.0452528 | 0.143452 | intron-variant | HECW1 | GRCh38.p7 | 7:43294907 | TACATTTTAGGGAGA[A/C/T]GTGAGACTTCAATCT | 23072 |
rs112099011 | snp | A/G | 0.470811 | 0.117228 | intron-variant | HECW1 | GRCh38.p7 | 7:43259280 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 23072 |
rs112114067 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43494622 | AATTCCTGAGCCTCA[A/C]CCTGACAAGTAACTG | 23072 |
rs112114163 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43196595 | GCCTCATTGATTTAA[C/T]GCCCTCAGGATGAGT | 23072 |
rs112114472 | in-del | -/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43255614 | AAAAAAAAAAAAAAA[-/C]AAGATTTATTCAATA | 23072 |
rs112132844 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43219585 | GAGAGGGTCATGATC[G/T]ATTGAGCAAGCAGTG | 23072 |
rs112134407 | in-del | -/TA | 0.0547245 | 0.156101 | intron-variant | HECW1 | GRCh38.p7 | 7:43191137 | TTAACACTCTTGGGT[-/TA]TATATATATATGCAA | 23072 |
rs112154556 | snp | A/G | 0.477004 | 0.104734 | intron-variant | HECW1 | GRCh38.p7 | 7:43488294 | CAGCCTAGGCAACAG[A/G]GTGAGACTCCATCTC | 23072 |
rs112166092 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43212364 | TTTTTCCTGCTATTA[A/T]TACTAAACAAAATTA | 23072 |
rs112166223 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43391235 | ACATATAGCTTAGAA[C/G]GTATGTAAGTTCTGG | 23072 |
rs112178933 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43270768 | ATTAGAATTAAAAAG[A/G]GTTAAATAATGTGGC | 23072 |
rs112179330 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43499527 | AAATCATCCATCTTT[G/T]ACCACTGGGAGAAAC | 23072 |
rs112184161 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515183 | ATGTCAGTTTGGTGT[A/G]GCCTCAGAAGAGAGA | 23072 |
rs112184698 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43430542 | CTTTTCCCATGATTG[A/G]CTGTTATACATTATC | 23072 |
rs112195403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43558488 | GGGGCTGGGGAAGGC[A/G]ACTTTGCCCCTCTTC | 23072 |
rs112198088 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562508 | CTCATGATTCACATG[C/T]GGCATCAGTCCCATC | 23072 |
rs112224289 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136727 | ACCCATCCAAACTGC[A/G]GATAAGAGAACTTTT | 23072 |
rs112226955 | snp | A/C | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147192 | TATTTTAATGTGCCT[A/C]TTCTGATTTCTCTAA | 23072 |
rs112227697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159841 | CCCACCACCACGCCC[A/G]GCTAATTTTTTGTAT | 23072 |
rs112235307 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43375144 | CTCCAAAAGGAGCCA[A/G]GGGGTTCCTGGAGGA | 23072 |
rs112241144 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125257 | TCCAACATGCGAATT[C/T]GAGGGGTGCAAACAT | 23072 |
rs112249820 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43280545 | GAATTGTAGTTCCTG[A/G]TGAGCAGAAATACAA | 23072 |
rs112253916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268923 | GGGACTACCAGTGTG[C/T]GCCACCAACCCTTGC | 23072 |
rs112254020 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139169 | TCTAGGAGGGAAATA[C/G]TGACCTGACCCTAGG | 23072 |
rs112255649 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131484 | TTTTGAGAGGAGTGG[A/G]TGTTAGAAACATTGA | 23072 |
rs112277275 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43366187 | CTTGTCAGACCCCCT[A/G]AGCAGAGGTAAGAGT | 23072 |
rs112285071 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43346963 | TTGCTTAATCTTGCA[C/T]TGGCTATGTGGGCTC | 23072 |
rs112291314 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43168984 | CTGAGAGCTTGGGTG[A/G]GGGGTGATTTCTTGG | 23072 |
rs112299565 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43327361 | CCCCACCGCTGCCCA[A/C]CCACTTTAGCACTAC | 23072 |
rs112299985 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43477861 | ATCTGTATAAAATTT[A/C]TTTTAACTACTTTTG | 23072 |
rs112311915 | snp | A/C | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152995 | TCCTCTGAGAATAAA[A/C]TTTCTGTTGATTGCT | 23072 |
rs112314750 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145231 | GTAGTCTGCATGGCC[C/T]CTTAAGATGATTAAT | 23072 |
rs112320238 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43533804 | ACCATGTGATCAGCT[C/T]TCCAGGCAGGAAGAC | 23072 |
rs112321952 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43336776 | CCCATTGTTTAGCTC[G/T]CACTTATACATTAAA | 23072 |
rs112327166 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43183805 | ATTCTTCTGGAATGT[A/G]AGTAACTATTTTGCT | 23072 |
rs112355364 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359074 | CAAATGATCCACCCA[C/T]CTCGGCCTCCCAAAG | 23072 |
rs112356805 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519578 | CTATGCTGGACTGCC[A/G]CACAAAACACCCAGG | 23072 |
rs112362678 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43371905 | GCTCACTGCAACCTC[C/T]TCCTCCCTGGTTCAA | 23072 |
rs112368615 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43212370 | CTGCTATTATTACTA[A/G]ACAAAATTATATACT | 23072 |
rs112372600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43403001 | GTTAAATAAATTACC[A/G]TAGAGCCAAATTATT | 23072 |
rs112372652 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43379734 | ATTCACTCCCTCCCC[A/C]CATTTAGATCGTTTT | 23072 |
rs112395659 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43263601 | CCTGACCTTGTGATC[C/T]GCCCGCCTCAGCCTC | 23072 |
rs112395795 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | HECW1 | GRCh38.p7 | 7:43401717 | GCCTACCAAGTGATA[C/T]GGACAGGAGACAGGG | 23072 |
rs112403069 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134988 | ACTTTACCTGAAACA[C/T]GAATTCTGATTTGCC | 23072 |
rs112404029 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128383 | TAGGGCCCTTAAGAA[C/T]TATGCTAAATCTATT | 23072 |
rs112404906 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43560261 | GTTCCCTTTCACTCA[A/C]ATATTTACATCTAGG | 23072 |
rs112407930 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | HECW1 | GRCh38.p7 | 7:43264717 | GGTGTGGTGGCGGGC[A/G]CCTGTAGTCTCAGTT | 23072 |
rs112409292 | in-del | -/T | 0.0573587 | 0.15934 | intron-variant | HECW1 | GRCh38.p7 | 7:43386860 | TCACATAAGGACAGG[-/T]TTTGTTTACAAAATA | 23072 |
rs112415157 | in-del | -/TACA | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43194426 | CCATAAAGCTAGTGT[-/TACA]TACAGCTCTTTTAGA | 23072 |
rs112429440 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43556424 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 23072 |
rs112447225 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43242885 | TAGCGTCCACCAGGG[C/T]GTTGGACACAGAGCA | 23072 |
rs112448326 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | HECW1 | GRCh38.p7 | 7:43340758 | CAGTGTGGCGATTCC[C/T]CAAGGATCTAGAACT | 23072 |
rs112449551 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508354 | CATGCACAAGAGGAT[A/G]TGCCAACAATACAGT | 23072 |
rs112459227 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43289900 | TAGATGGGTTTTAGG[A/G]ATTCTTTAGTTGACA | 23072 |
rs112460261 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43328669 | GTCCCTCAGATTAAA[C/T]AACAAAGCATGACTG | 23072 |
rs112461540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132173 | CTCACAGCGCCCCCC[C/T]GCCCCAAGTAAGGTT | 23072 |
rs112472385 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43258350 | TCCATCTCAAAAAAA[C/T]AAAAAATAAAAAAAA | 23072 |
rs112473134 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43172161 | CACAATGGTGGGGGT[C/G]GGGGGATGTGTAATC | 23072 |
rs112478631 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43468758 | AATTCCTGGGTGTTT[A/T]CTTCTTGAGCAAGAG | 23072 |
rs112480335 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154518 | GTGAATTATATTCTC[A/G]TTGTAGTAATCAGTG | 23072 |
rs112492134 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43503632 | TCTCTAGCATTGACC[-/A]CAGGGTCCTAGAATA | 23072 |
rs112495941 | in-del | -/CGAGAGT | 0.447421 | 0.153379 | intron-variant | HECW1 | GRCh38.p7 | 7:43422927 | ATCGCAGTGCCTGGC[-/CGAGAGT]CGAGAGTCGTGGTCT | 23072 |
rs112498825 | snp | C/T | 0.188 | 0.24219 | intron-variant | HECW1 | GRCh38.p7 | 7:43394953 | AGCCAGGAATGCTGA[C/T]TGGTCAGAGATGAAA | 23072 |
rs112501528 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43265726 | CTACAGGTTAAAGGC[A/G]CATTCTCACAAGGCT | 23072 |
rs112511775 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296413 | GCTTTTCTTGTTGCC[C/T]AGGAAGGTCTATGGT | 23072 |
rs112520074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43548115 | ACCATGTACAGGCTC[G/T]AAGTGTTTGTGTGTG | 23072 |
rs112522739 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43307882 | ATCATTTCACTATAT[A/C]TATATATATATATAC | 23072 |
rs112527993 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43355858 | GCTGGGTGTGGTGGC[A/G]CACACCTGTAGTCCC | 23072 |
rs112530363 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43369504 | ATTTGACAGTCTTGG[A/T]ACTGTTAAAAGTCTA | 23072 |
rs112545587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43216935 | GCTGGGATTACAGGC[A/G]TGAGCCACCACTCCC | 23072 |
rs112546948 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43368419 | AGCTTATTCATAAAT[A/G]TGTCTCCTGCAAAAG | 23072 |
rs112552733 | snp | C/T | 0.142947 | 0.22592 | intron-variant | HECW1 | GRCh38.p7 | 7:43251395 | GCTCACTGCAACTTC[C/T]GCCTCCCAGGTTCAA | 23072 |
rs112555217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207110 | GGAGTCCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 23072 |
rs112557061 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43327893 | GCAAGATTAAAGGCA[C/T]GGCAGGGTGGAGCTG | 23072 |
rs112558368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369256 | CTGAGGTCAAGAGTT[C/T]GAGACCAGCCTGACC | 23072 |
rs112562816 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128671 | TAAGAAATACATTTC[C/T]TGATGCTATAGCTGC | 23072 |
rs112569663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43169789 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 23072 |
rs112578528 | in-del | -/T/TTT | 0.378765 | 0.214288 | intron-variant | HECW1 | GRCh38.p7 | 7:43284998 | TGCTTTCTGTATGGA[-/T/TTT]TTTTTTTTTTTTTGC | 23072 |
rs112605125 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308343 | ATTTATATATATTAT[A/T]TGATATATTTATATA | 23072 |
rs112611846 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514864 | CCTACTTTTACAGAT[A/G]AGGAAAATGAGGTGC | 23072 |
rs112620860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191726 | TTGCTAACTCACTAT[A/G]TATGCTTTTACATTG | 23072 |
rs112623426 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43457525 | CGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCTGA | 23072 |
rs112625913 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43332853 | TGCCTCATTTAATCC[C/T]TATGGAACCCTAGAT | 23072 |
rs112627563 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43506455 | TAAATATTTATTCTC[A/G]TTAGAACTCATAAAT | 23072 |
rs112645278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43464912 | GCTCAAACAGTCCTC[C/T]CAACACAGCCTCCTG | 23072 |
rs112646344 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139887 | GGGTGTCTTAGGTGA[A/G]TTGTTTAACCATTCT | 23072 |
rs112648367 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43310809 | AACTTCATGAGTCAA[C/T]ACTTTTTTAGGCCTT | 23072 |
rs112650676 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43498014 | AGTTCTCCCGATGGT[C/T]AAGGGATATATGTAG | 23072 |
rs112654925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43461933 | ATAATACTTCCTAAA[A/G]AACTCGTTAGAAATG | 23072 |
rs112655228 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43468363 | TGAGGCTCAGGCAGG[C/T]AGAGGGAGGCCAAGG | 23072 |
rs112668179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225869 | AGCTGTCTGCAGCTT[C/T]GACTGATCATCCTGC | 23072 |
rs112673261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43536863 | GACAGCAGGACAACA[C/G]GGAGGAGCCACTCCC | 23072 |
rs112678392 | in-del | -/AAAAAAAAA | 0.36021 | 0.224397 | intron-variant | HECW1 | GRCh38.p7 | 7:43186669 | GCGAGACTCCGTCTC[-/AAAAAAAAA]AAAAAAAAAAAGGAT | 23072 |
rs112680762 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | HECW1 | GRCh38.p7 | 7:43264830 | GCCCGGGCGACAGAG[C/T]GAGACTCGGTTTAAA | 23072 |
rs112686884 | snp | G/T | 0.194278 | 0.243711 | intron-variant | HECW1 | GRCh38.p7 | 7:43398190 | TGAACATGGGAGGTG[G/T]AGGTTGCAGTGAGCC | 23072 |
rs112689373 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43244840 | CAAATTTATTAAGCA[C/T]ATCCACATGCATATT | 23072 |
rs112699252 | snp | A/C | 0.112631 | 0.208878 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125566 | TCGAGACCAGCCTGG[A/C]CAATATGGTGAAACC | 23072 |
rs112710575 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43448711 | TTCAAGGGAAATTTT[C/T]ACATTATTAGGTATA | 23072 |
rs112717443 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43547824 | CAGCATCATTAGTGG[A/C]CCTTCGTGTGGGTCC | 23072 |
rs112723902 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43285039 | TCATATTTGAATTTA[C/T]TAAGTGTAGTTATAT | 23072 |
rs112724152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43179517 | CCCATTAAAAGAAAT[A/G]CCATTGGTTATTTGG | 23072 |
rs112748986 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43489214 | TTCCCTCTGTAATTT[A/G]TCACTTAGATAACCT | 23072 |
rs112755147 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43190103 | TTGTTGTTGTTGTTG[-/T]TTGTTTGTTTGCTTT | 23072 |
rs112760529 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HECW1 | GRCh38.p7 | 7:43188034 | GAAGGACTAATTCCA[A/G]CACAAACATAACAAA | 23072 |
rs112775157 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43309323 | TGGGGTGCAAGGGAC[A/G]GCTTTGAGGCTGCCC | 23072 |
rs112778200 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43545489 | GACCCTTCAAAATGC[A/G]AAGGTTAGGGCGCTG | 23072 |
rs112778473 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514380 | CTGCAACCTCCACCT[C/G]CTGGTTCAAGCAAGT | 23072 |
rs112781818 | in-del | -/C | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375892 | TGAGACCCTTCTCAA[-/C]AAAAAAAAAAAAAAA | 23072 |
rs112789561 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43559373 | CTGCCAGTAGGTCAC[A/G]TGCAAAACTCCAGAG | 23072 |
rs112790033 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43308765 | TAGCTGGGATTACAG[A/G]CACCTGCCAACACGC | 23072 |
rs112801221 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43500398 | CCACTGTGCCCCGCC[A/C]CAGAACAGTCTTTCA | 23072 |
rs112802791 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43478583 | TAATTTAGGGAAATA[C/T]TTATAAAATAACAAG | 23072 |
rs112812992 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43209708 | CTTTCCACAAGTGCT[G/T]GGAAGGAGAAAAGAA | 23072 |
rs112820454 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299914 | TGCTAATAAAGCAAT[A/G]TGCCACTCATCTAGG | 23072 |
rs112824237 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43537604 | GCTATTGTTTTATTT[C/T]CCTTCAGCTATTGTT | 23072 |
rs112825788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43340377 | AGTCGCCAGCCATCA[C/T]GCCCAGCTAATTTTT | 23072 |
rs112827036 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302489 | TAGCCAAGCAGGTGG[C/T]GGTGCCCTGGTTACG | 23072 |
rs112835887 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43351681 | TTTTTCTTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs112839390 | snp | A/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43336985 | GACTTTGCTATTGTG[A/T]ATAGTGCTGCAATAA | 23072 |
rs112840442 | snp | A/C | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43256570 | GCCAAGATTGCGCCA[A/C]TGCACTCTAGCCTGG | 23072 |
rs112858496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244670 | CTGAAGTCTCCCAGT[A/G]GGTAACTGAGGAGCA | 23072 |
rs112861434 | snp | C/T | 0.190833 | 0.242898 | intron-variant | HECW1 | GRCh38.p7 | 7:43486349 | TGGAGTGCAATGGCA[C/T]GGAGTGCAATGGCAC | 23072 |
rs112862656 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43210556 | GGCTGCAAGCCTCGT[G/T]TTCGCTAACCTGGGG | 23072 |
rs112878549 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43235074 | CTTGATGGCACTAGT[C/T]CCTTGGAAGCCAGCC | 23072 |
rs112881053 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114688 | ATTCCACACTATAAT[C/T]CCAGTCTAGTGCAGT | 23072 |
rs112882737 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43180742 | ATTATACATGTTTAT[A/G]AAGTACAATGTGATG | 23072 |
rs112883775 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43258198 | TACAAAAAAATTAGC[C/T]GGGTGTGGTGGCACA | 23072 |
rs112892664 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | HECW1 | GRCh38.p7 | 7:43381551 | TGGAGTGCAGTGGTG[C/T]GATATCCGCTCACTG | 23072 |
rs112898979 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | HECW1 | GRCh38.p7 | 7:43368148 | CAAATCCCCATGCTC[A/C]TCAAGCCACCTGCCT | 23072 |
rs112917465 | in-del | -/TCTG | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43306291 | TGCTACTTCCTGATT[-/TCTG]TCTGTTTTGTATTTT | 23072 |
rs112925368 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43192160 | GATGGGGTTTCACCA[C/T]ATTGGCCAGGCTGGT | 23072 |
rs112940975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43242428 | AGAAAGAGGACTGGA[A/G]AAAGAAAGCTGTCCA | 23072 |
rs112942689 | snp | A/G | 0.00743501 | 0.0605163 | missense | HECW1 | GRCh38.p7 | 7:43444668 | AGAGCCGGGCTGGAA[A/G]GGAAGAAGAGGAGAA | 23072 |
rs112943825 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43279501 | TAACCCGACCATCCA[C/T]GCTCTTCTTTTTTAC | 23072 |
rs112966559 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43418370 | GAACTTCTTGAAGCT[A/G]TAAGTTTGTTTTCAC | 23072 |
rs112974558 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213993 | TGGAATTTATTATAT[A/T]AGACCTTTAGAGACC | 23072 |
rs112985555 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144067 | ATGCCAAATGACATC[A/G]AGTCATCATGTCTTC | 23072 |
rs112987976 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211046 | TCCCTCCTGCAGTGC[-/T]CTCAGGCGATAGATG | 23072 |
rs112995244 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43315557 | AGAGTACAATGGCAC[A/G]ATCCCAGCTCACTGC | 23072 |
rs113010164 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43347941 | TTTTGTTAAAGATTT[C/T]AGCATCTATGTTCAT | 23072 |
rs113012352 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43450683 | CACGAATGACTGTGA[A/G]TGTAGCAAACTGACA | 23072 |
rs113016795 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129647 | AACAAAACGGATAAA[A/G]GACAAAATAACCATC | 23072 |
rs113023661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529574 | CATCAACCAAAATCA[C/T]GTCCACTGTGAGATG | 23072 |
rs113024278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152518 | TATTCTTTTTTATAG[A/G]CTCATATTCCTGTTT | 23072 |
rs113029185 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308005 | TAATATATAATATAT[A/G]ATATACAGTATATAT | 23072 |
rs113029357 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519583 | CTGGACTGCCGCACA[A/G]AACACCCAGGTGTGT | 23072 |
rs113037564 | in-del | -/G | 0.0283406 | 0.115616 | intron-variant | HECW1 | GRCh38.p7 | 7:43217948 | TTCTGGGGCTGGAGA[-/G]TGCAGGATTTCCTCG | 23072 |
rs113041729 | snp | A/C/G | 0.00835572 | 0.0641442 | intron-variant | HECW1 | GRCh38.p7 | 7:43286682 | CTGCCACCCACCCCC[A/C/G]CAAAGGTGTTTGGGA | 23072 |
rs113043572 | snp | C/T | 0.178785 | 0.239642 | intron-variant | HECW1 | GRCh38.p7 | 7:43500333 | TTGAACTCCTGATCT[C/T]GTGATCTGCCTGCCT | 23072 |
rs113045376 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300849 | GCAGGTACGATGACC[C/T]CCCACACTGATGTGA | 23072 |
rs113053320 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43489794 | AAAGGAAAATCAGCA[A/G]TGCCTGTGTTTGTCA | 23072 |
rs113053695 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43204825 | CTTTAGGACAGGACA[G/T]AGTTTTGCCAACTGG | 23072 |
rs113060406 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43312530 | TGCTTTGTATTCAAC[A/C]GACAAGCTGGGATTA | 23072 |
rs113065442 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268448 | TGATTTTGTCCCCCG[C/T]GGACATTTGGCAATG | 23072 |
rs113072751 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43283703 | ATGTAAGAGTAACAT[A/G]TATTGTTCAATATTG | 23072 |
rs113088765 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43489522 | AAACCCTGGTGTCTG[G/T]CTTTGCCAGCTGAGC | 23072 |
rs113094638 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43470414 | CCTTGGATTTCCATG[A/C]CTGCAGCTTTTGCAC | 23072 |
rs113095761 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302953 | TGCACACACACATGC[A/G]CGCACACACACACAC | 23072 |
rs113103822 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43363498 | ATCAGTAGACACTTG[C/G]GTTGACACTTGAATG | 23072 |
rs113105354 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375804 | GGACTATGGTGAGAG[A/G]ATTGCTTGAGCCCTG | 23072 |
rs113120962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43410974 | ACATCATTTTCTCTA[C/T]GTTTAACTGTTTTCT | 23072 |
rs113121717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43320207 | ATTCGAAGTGGAGTC[C/T]GTGAGAACTAGACCC | 23072 |
rs113124593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156590 | ACCTGAGATAGTAGG[C/T]TGTCATTAGTGAGTA | 23072 |
rs113125240 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43401155 | AGGATGTGAACATCT[C/T]TGTGAGGTCATTATT | 23072 |
rs113135065 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137872 | GCTTTCTTTATCACC[C/T]GTTTAGATCTTACTC | 23072 |
rs113135124 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130009 | TCTGCAGTTGGTTGA[A/C]TCTACAAATGCAGAA | 23072 |
rs113149364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256326 | TAGTAAAGATGAACA[A/T]CGGCTGGGTACGGTG | 23072 |
rs113151243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43201538 | AGAAAAACAGTAACG[A/G]AACAGCCAGTGTTCA | 23072 |
rs113161737 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515730 | CAGATTATAGTAGCA[C/T]ACTCCCAGATGCTGT | 23072 |
rs113168129 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128201 | AGATTTTCAATGCAG[A/G]TAAAACAACCTTCTA | 23072 |
rs113168927 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213046 | GTAATGAAATTAGTA[A/T]TATGTCAATTTTCTT | 23072 |
rs113179521 | snp | G/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142089 | CTATGATAGAGAAAA[G/T]TCTCTGAGGACTTGA | 23072 |
rs113183441 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43464686 | ATGCAGAATATTGGA[C/T]ATTTTCATGTGATTT | 23072 |
rs113183444 | in-del | -/A | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43487952 | AACAGAGACTGTCTC[-/A]AAAAAAAAAGGAAGA | 23072 |
rs113205211 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | HECW1 | GRCh38.p7 | 7:43388747 | CATGCCTCAGCCCCT[C/T]GAGTAGCTGGGATTA | 23072 |
rs113216766 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43435891 | ATTGCTAGGCCGGGC[A/G]TGGTGGCTCACGCCT | 23072 |
rs113223615 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43460016 | GCTTGTATAGTATTC[C/T]ACTGAATGGCTGAAG | 23072 |
rs113226290 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43453507 | TGTGTTTGAGATGTC[A/G]TCCAGGTAGTAATGT | 23072 |
rs113227518 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43245869 | AAAGCTCCTTACCCC[A/G]CACCTTACTCAGTAA | 23072 |
rs113230750 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43478192 | GAGGGCGAGGTGGGC[A/C]GATCACCTGAGGTCA | 23072 |
rs113240115 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43336872 | CACGTTGCTGCGAAG[G/T]ACATGATTTTATGTT | 23072 |
rs113244442 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43235721 | TTCTGGAGGATGGCC[A/C]GTGGGTCTCAGTATT | 23072 |
rs113247707 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269521 | TGAAATTCACACTTG[A/T]AGCATATTTGGGTTA | 23072 |
rs113261701 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142455 | CTGGGGGAAGTTACC[G/T]CCTCCCTTCCGAGGG | 23072 |
rs113263522 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43173274 | CATGGCTAAGCAGAG[A/G]AAGAATGGTTTTGCT | 23072 |
rs113274595 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43440864 | ACTAAATCATGGCTT[A/G]TCAAAGAACAATTTT | 23072 |
rs113276517 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43184652 | ACGGGCTAAAGGTTG[A/T]GTTGATCACCAATGG | 23072 |
rs113278958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43449841 | CTCTGCAAAGATCAA[A/G]AGCACTGGCCTCTGA | 23072 |
rs113284154 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43186521 | AAATACAAAAAAATT[-/T]ACCCAGGCTTGGTGG | 23072 |
rs113290289 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | HECW1 | GRCh38.p7 | 7:43182064 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCA | 23072 |
rs113312677 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43506513 | AGTATATTATTTCTA[A/T]TTATTATAAAAGTCA | 23072 |
rs113316074 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43256566 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCTAGC | 23072 |
rs113317114 | snp | A/G | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268495 | ATTGTCATGACTTGG[A/G]CATGCTACTGGACCT | 23072 |
rs113325011 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43493869 | ACTATTGATGGAGGC[A/G]TGTTATTCAACTCTC | 23072 |
rs113330662 | snp | C/T | 0.5 | 0 | intron-variant, splice-acceptor-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512125 | GAGATTCATGGAGGC[C/T]GTGAAGAGGATGACA | 23072 |
rs113332407 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43293155 | AACCCGGGAGGCGGA[A/G]GTTGCAGTAAGCCGA | 23072 |
rs113334195 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43554150 | GTTCGCCTCCAGCCT[A/G]GACTGGTAAGTCCTA | 23072 |
rs113341544 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43358181 | TGATCCCACCGGCAC[C/T]TACAGGCAGAGTAAC | 23072 |
rs113347693 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43314227 | TGGGGAGAAGGTAAT[A/G]AGCTCAAGATGGAAT | 23072 |
rs113348394 | snp | C/T | 0.00435466 | 0.0464582 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43554596 | GCCTCGTGCAGGTTA[C/T]CACGATGGGCATCTT | 23072 |
rs113356211 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43437892 | ACCCTTTATATATAG[A/G]TATATTATAGCTAGG | 23072 |
rs113388630 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43245051 | GTTCTGCCTAATGCA[C/T]TTAAAGAATGAGCAT | 23072 |
rs113393628 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214812 | CAGCTCACAGCCCAC[A/G]GTGAGGGAACCATGT | 23072 |
rs113401261 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159728 | TCTGTCGCCCAGGCT[A/G]GAGTGCAGTGGTGGC | 23072 |
rs113402572 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43553688 | AAAAAAAAAAAAAAA[A/G]GTCTCTGCCTGGCTG | 23072 |
rs113412764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43447407 | AGTGTTTCAGGGTCA[A/C]AGTGGACATCTCTGA | 23072 |
rs113413808 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43227075 | AGTCAATGCCTCTCT[C/T]ATTAATGTCTCATTA | 23072 |
rs113423662 | snp | A/T | 0.5 | 0 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297749 | TACAGTGGAGTCACT[A/T]GAAAACAACATAGTG | 23072 |
rs113429370 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43325572 | ACTGACCTCTGATTA[A/C/T]AGCAAAAAGAGACCA | 23072 |
rs113431810 | in-del | -/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43380534 | GGTGAATGTATGTGA[-/T]TTTTTCCCCCTAGAT | 23072 |
rs113434284 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43285223 | CTTCCTGGGATTAGA[C/T]ATGTAGACAAACTGG | 23072 |
rs113448724 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129833 | ACCTGCCCATAAGCT[A/G]CATACATCCTCCTGT | 23072 |
rs113461334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43370297 | CTGCAAATTAAAACA[A/G]TGAGGTACCAAAGAT | 23072 |
rs113463870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134644 | CTAAGTAGTTGGGAC[C/T]ACAGGCATGCACCAC | 23072 |
rs113471017 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43468515 | GGGGGCATGATTCAA[C/T]GCACATTCACTTTTT | 23072 |
rs113476634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43361224 | CACTTGTGTGTTAGG[A/G]AGGAGCCAAGCTTCT | 23072 |
rs113480971 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139757 | TCCAAGTTTGGTTTC[A/G]TTTCTCTTAATTGCT | 23072 |
rs113490996 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43486768 | GTATGAACAATATGT[A/G]ATGAATGCAGAATAC | 23072 |
rs113504228 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43448074 | CAGGAGGCAGAGGTT[G/T]CAGTGAGCTGAGATC | 23072 |
rs113512274 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | HECW1 | GRCh38.p7 | 7:43251646 | TTTCTACTTATTATA[C/T]TCACAGGTCTAAATA | 23072 |
rs113515271 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43313956 | TGGTTTGATTTGGTT[G/T]GGTTTTGGTTTTGGT | 23072 |
rs113519082 | in-del | -/C | 0.327211 | 0.237778 | intron-variant | HECW1 | GRCh38.p7 | 7:43237833 | AATTCACCAGTCTTT[-/C]CCCCCCGCCGCCCCC | 23072 |
rs113533560 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43173275 | ATGGCTAAGCAGAGG[A/G]AGAATGGTTTTGCTA | 23072 |
rs113534901 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43364239 | CATTGTATGGTCTCA[C/T]GATGCATCAATTCTT | 23072 |
rs113539734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351377 | TTTCCAGAGAGTTTC[A/G]GCTGTAGTAGTATGC | 23072 |
rs113543455 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43273065 | TAAGCAAATTAGTGC[A/G]GGAACAGAAAACCAA | 23072 |
rs113543852 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43289916 | ATTCTTTAGTTGACA[A/G]TTGGTTGAGAGAGTT | 23072 |
rs113548900 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | HECW1 | GRCh38.p7 | 7:43321911 | ATCCCCGCTCCCGGC[A/C]ATGACACCAATAGCT | 23072 |
rs113554750 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211824 | TTCTGTTTCTGCCTT[A/G]TACACCTCAGTTAAG | 23072 |
rs113558258 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43436294 | GTTAATTAAGACTTC[C/T]TCTTCCCAGGTAGTT | 23072 |
rs113573368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516980 | GGTACACCTGTATAG[A/G]GCAGCTCCGTTATAA | 23072 |
rs113574494 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43237920 | GGAAAGTTAAATGAG[A/G]TACTGAAGCCGATGG | 23072 |
rs113581705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43463359 | TCTTATTTTAGACTT[A/G]GCCTGATTTTGTTTA | 23072 |
rs113582169 | snp | A/G | 0.208779 | 0.246578 | intron-variant | HECW1 | GRCh38.p7 | 7:43351381 | CAGAGAGTTTCGGCT[A/G]TAGTAGTATGCAGAG | 23072 |
rs113585801 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43210278 | ACTTATTGTGGAGAT[A/G]GGTCATTGAAAAGGT | 23072 |
rs113595513 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43451055 | AGTGTTAACAAAGAC[C/T]AATATGACACCTGCT | 23072 |
rs113599509 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43372407 | GTACATGTGCACAAC[A/G]TGCAGGTTTGTTACA | 23072 |
rs113610829 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211435 | CGGGCACCCTGTGGA[C/T]GCTAGGGATGCAGGG | 23072 |
rs113615566 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43534666 | GGTTTGTATAGTTGC[A/G]CTCCACTGGGATAAA | 23072 |
rs113616785 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43317625 | GGTAACAAATGCCTT[C/T]GGGGAAGGGTTTGAC | 23072 |
rs113617473 | snp | G/T | 0.0310518 | 0.120672 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112030 | TAACCAGCATTTCAC[G/T]TCTCTTTGCATCTCA | 23072 |
rs113623416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43487426 | AATCCTAAAAGTAGT[C/T]CCTACTACAAACTGG | 23072 |
rs113628897 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520510 | CTCATTTACATGGGC[A/G]CAAATTTCCTACCCT | 23072 |
rs113630900 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43283892 | ATTTCTCCTACCTGA[A/G]CGTGTCATTTCTGAA | 23072 |
rs113631805 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126515 | ATTAGACCCACAAAA[A/C]CTTAAATGTTTACTA | 23072 |
rs113632012 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43320089 | GTTAGATTTCAGCTG[C/T]TGAATGAACAATGAA | 23072 |
rs113632216 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43549193 | ATTTACTTACATGCC[A/G]CACCTAGCTGTGAGA | 23072 |
rs113633599 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43335779 | TCTTTTTTCTTTCTT[C/T]CTTTCTTCCTTCCTT | 23072 |
rs113633957 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43322693 | AGCAAGTGGTACCTG[A/C]TATAAACCTCCTAAA | 23072 |
rs113640791 | snp | A/G | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111359 | CCAAGTGTAAAATCC[A/G]GAGAAATGTGTGCAC | 23072 |
rs113643717 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123829 | GAGTGGAGGCTGGAA[A/G]ACCAGGCCCTCCTCT | 23072 |
rs113644926 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134319 | GAACCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 23072 |
rs113659306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43481938 | CGAGATGGCACCACT[G/T]CACTCCAGCCTGAGC | 23072 |
rs113664262 | in-del | -/GTAGGTAG | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43237141 | GAAGGAAGGAAGGAA[-/GTAGGTAG]GTAGGTAGGTAGGTA | 23072 |
rs113691110 | snp | C/T | 0.195526 | 0.243993 | intron-variant | HECW1 | GRCh38.p7 | 7:43486491 | TATCTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 23072 |
rs113713516 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248766 | TCTTCCCCCATCTCC[C/T]CGTTCTCCTCCTGTT | 23072 |
rs113717921 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523379 | TTGGCTTTGTGGGGC[C/T]GCTAGAAGGATGCAA | 23072 |
rs113720300 | snp | G/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43219136 | AGGGCGCCATGATGT[G/T]CTACACATGTGGGGA | 23072 |
rs113722407 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43538861 | CTGACAGAATATTGT[A/G]AAGAGTGGTAGTAAC | 23072 |
rs113726032 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137671 | CCTCCCACCTCAGCC[C/T]CCCGAGTAGCTAGAA | 23072 |
rs113727579 | snp | A/C/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43415158 | TCATGATTTTGCAGC[A/C/G]GCTGGTACCGGTTGT | 23072 |
rs113733039 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120877 | TGGAACTCCTGGCCT[C/T]GAGTGATCTGCAAAT | 23072 |
rs113734135 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43499335 | CTAGCTGAGTGTGGC[A/G]GTGCATGCCTATAAT | 23072 |
rs113737366 | in-del | -/AC/CT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43198076 | CACCCCACACACACA[-/AC/CT]CTCTCTTACACACCA | 23072 |
rs113752664 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416428 | GAACCACTGCTCTCT[A/T]CAAAGCTGTCAGACA | 23072 |
rs113758084 | snp | C/T | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134168 | CACTTTGGGAGTGGG[C/T]GGGTCACCTGAGGTC | 23072 |
rs113758552 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43321924 | GCAATGACACCAATA[A/G]CTCTTTCTTGTGTTG | 23072 |
rs113760337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43291073 | TAGTTTTCTCCTCCA[C/T]GCTGTTATATGTACA | 23072 |
rs113767366 | snp | C/G | 0.194902 | 0.243853 | intron-variant | HECW1 | GRCh38.p7 | 7:43397796 | CTTCAGTTGCTTCAG[C/G]TCATCTGGATGTATA | 23072 |
rs113767906 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211018 | CTGGGTTTGTATCCC[G/T]GTCATTGTATTGTCC | 23072 |
rs113778236 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | HECW1 | GRCh38.p7 | 7:43188031 | TAGGAAGGACTAATT[A/C]CAGCACAAACATAAC | 23072 |
rs113781250 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360050 | GCACTTAATTGAATC[A/G]AAGCACTTTTATTTG | 23072 |
rs113795852 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43414229 | GCAATTGTGAATGGG[A/T]GTTCACTCATGATTT | 23072 |
rs113797609 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43535380 | GCCGTAAGAGCCCTC[C/T]ATGTGTTTTTGAAAG | 23072 |
rs113810087 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43529970 | TTATTTTTTTTTTGA[A/G]ACAGAGTTTCGCTCT | 23072 |
rs113812973 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138165 | ACCCTCCAACTGGGA[A/G]AGGTAATGAAAGAAG | 23072 |
rs113813603 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151915 | ATACAAGATATTGAA[A/G]AAGACACATACATAT | 23072 |
rs113816333 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | HECW1 | GRCh38.p7 | 7:43459630 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC | 23072 |
rs113827765 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43305770 | CGCCCAGCTAATTTT[A/G/T]TTTTTTTGAGACGGA | 23072 |
rs113829179 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43533644 | AGAGGCCTTTATAGA[C/T]TAACGACTGCGTGCA | 23072 |
rs113829917 | in-del | -/T | 0.230603 | 0.249246 | intron-variant | HECW1 | GRCh38.p7 | 7:43273858 | TGTAAAATATGATTC[-/T]TTTTTTTTTTTTTGA | 23072 |
rs113831031 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43546312 | GGGAGGTTATGCATA[A/G]CATTTGGACACAGTT | 23072 |
rs113835063 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43306361 | CTCAAATCCTTTGTA[A/G]AAAAAGATAAGCTTT | 23072 |
rs113836264 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43304323 | GTGCAGTCCAGGAAC[C/T]AGGAACTCAATTCGA | 23072 |
rs113837549 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562616 | GATGCAATGCAATGC[A/T]TCCCAATGGTTGTGG | 23072 |
rs113846433 | snp | A/C | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147317 | ATTGAGCTTTACACC[A/C]TTTCATCCAATTGAA | 23072 |
rs113857414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192925 | AAGTAAAGTCATAAA[A/G]GGGTGGCTACTCCAT | 23072 |
rs113861063 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137239 | CCTCCCTCCCAGCAG[A/G]CATGTCAATCCCAGG | 23072 |
rs113866271 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43360695 | GTTAAGGCCAGAACA[A/G]TTTTTCATGTCACAG | 23072 |
rs113880860 | snp | A/C | 0 | 0 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43270248 | GGCTGGCAGGTTTAG[A/C]CTTCGGATCTCTTAG | 23072 |
rs113881026 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43274664 | GAGAGAGAGAGAGAG[A/C]GAGAGAGAGCGCGCA | 23072 |
rs113884072 | snp | A/C/T | 0.000132501 | 0.00813856 | synonymous-codon, missense | HECW1 | GRCh38.p7 | 7:43469016 | CGCTACCAGCACAAC[A/C/T]GGGACTTGGTGAATT | 23072 |
rs113890616 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | HECW1 | GRCh38.p7 | 7:43448814 | GAAGGGAATTTAAAA[C/T]GACGTTGCTTGCTTT | 23072 |
rs113895521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191026 | GCTATCCCAGAAATC[A/G]CAAAACAAAAAGGCT | 23072 |
rs113898752 | snp | C/T | 0.136166 | 0.22258 | intron-variant | HECW1 | GRCh38.p7 | 7:43262247 | ATATATGTATGTGTG[C/T]GTGTGTGTGTGTGTG | 23072 |
rs113900335 | snp | C/G | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125651 | TAATCCCAGCTACTT[C/G]GGAGGCTAAGGCAGG | 23072 |
rs113906638 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43507002 | TTGAACCCAGGAGGT[A/G]GAAGTTGCGGTAAGC | 23072 |
rs113916144 | snp | C/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43211956 | AATGACTTTACCTCT[C/G]CCTGTCTACTATGCA | 23072 |
rs113933913 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43560803 | TGTTTCTTTGTATGT[C/T]TGTTTTGTGATTTGA | 23072 |
rs113934535 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43553494 | ACCAGCCTGGTGAAA[C/T]CCTGCCTCTAAAAAA | 23072 |
rs113939621 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43167201 | GGAGGATCCTCCCCT[A/G]TCCTCTTCCAGCTCC | 23072 |
rs113950243 | snp | A/G | 0.5 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136004 | TTTTTACTATTTGCT[A/G]ATAGCTCCTTTTCAA | 23072 |
rs113958933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43477295 | AATATTTTTCTAACT[C/T]TAACCAAGTAATTAA | 23072 |
rs113961434 | snp | A/C | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43215562 | GTATTTTTAAACTTC[A/C]AAGTTGTATTATTAA | 23072 |
rs113961627 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43183970 | CACAATTTAAAAAAA[A/C]AATCAAGATGTGATT | 23072 |
rs113965284 | snp | C/T | 0.141596 | 0.225274 | intron-variant | HECW1 | GRCh38.p7 | 7:43251595 | TGCTGAGATTACAGG[C/T]GTGAGCCACCATGCC | 23072 |
rs113969727 | in-del | -/CT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43196810 | ATGGTGGTTTTAAAA[-/CT]CATATGAAGAATAAT | 23072 |
rs113973615 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43460087 | TTGCTTTTGTCACTG[-/T]TTTTTGTCACAAGGG | 23072 |
rs113976321 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43209116 | TTTCATGCCAGCTCA[A/G]CTTGCCCTGTGGTGT | 23072 |
rs113978915 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43401439 | AAACTGAACAGAAAC[A/C]GTAATAGAAGAAAAC | 23072 |
rs113983143 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43499982 | CTTGGGGCCGGGCCC[C/T]CTCTGTGCCCAATGT | 23072 |
rs113988593 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298006 | TTGAGCCAGGAATTC[A/G]AGGTTGCAGTGAGCT | 23072 |
rs113993680 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43555703 | TTCACCTGGTGTCGG[A/T]CAGCATTCATGGGCA | 23072 |
rs113998739 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43496197 | AAACTTGGAAATTAT[C/T]TAGTATGGAAACTAA | 23072 |
rs114015057 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43537636 | TAGATTTGAATTGTA[C/T]AGTTGCTGTATTTTG | 23072 |
rs114023619 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | HECW1 | GRCh38.p7 | 7:43454613 | CATAAGTTAAGTTTG[C/G]TGTTTGGGGATACTT | 23072 |
rs114024452 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43237758 | AACTCCCTAAGAACA[C/T]AAGCAAACCACCCCT | 23072 |
rs114032047 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43410524 | ACACACACACACACA[C/T]TCAGTCTATAACAGG | 23072 |
rs114062247 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | HECW1 | GRCh38.p7 | 7:43350556 | GAGGCTTTGTTCATG[C/T]TTTCTTACTCTTTTT | 23072 |
rs114081619 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HECW1 | GRCh38.p7 | 7:43255221 | GCAAAAGAGTTTGAA[A/G]TAAAAATAGCTGGAG | 23072 |
rs114084437 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43379788 | GGCCTTACATCACCA[C/T]CCTATCTAAACTATT | 23072 |
rs114110078 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298427 | TAGCAGTTTACAGTC[C/T]CCCTGACATGTGCTT | 23072 |
rs114125656 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121985 | TTCTAGAATGCTATA[C/T]GCCATGTTGTGTCCA | 23072 |
rs114126980 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142896 | TCGACAGGTCCCAGA[C/T]CTGTAAAATCGACAG | 23072 |
rs114144833 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | HECW1 | GRCh38.p7 | 7:43447584 | TGAAGGCCATGCACA[C/T]GCTGGCATGTGACTT | 23072 |
rs114149256 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43329727 | ACACGGCGTGCTAAG[C/G]AGAAGAACCCGGCTT | 23072 |
rs114156023 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148736 | TCAAGTTTACACTCA[A/G]TTGATCAAGTCCCTT | 23072 |
rs114161406 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43264573 | ATTGTCAGCCAGGCG[C/T]GGTGGCTCACGCCTG | 23072 |
rs114170153 | snp | C/T | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248754 | TTCTCCTGTCCCTCT[C/T]CCCCCATCTCCCCGT | 23072 |
rs114173093 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43206413 | TTTTTTCTGGTCTTT[C/T]ATTTTTTGTCTCTTC | 23072 |
rs114177514 | snp | C/G | 0.0279526 | 0.114869 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148642 | TTGGATTTCTCTAGA[C/G]AATGGATCAATCAAA | 23072 |
rs114189403 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148481 | TCCATCTAGTAGCTC[C/T]TGTCTTCACTGTGAT | 23072 |
rs114191674 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510930 | TTAAAAGTGGCCTCC[A/G]TCACTTTCCACAGTG | 23072 |
rs114196393 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43201151 | TCCATCACACACTGG[C/T]CCTTGGTGTTCCTTT | 23072 |
rs114214270 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43547717 | GAAAAGATGGGCAAC[C/T]ACATCTGCAGACCTC | 23072 |
rs114217463 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43356820 | AAGAAAAAAGTTTTA[A/C]AATTTTTTGAAACAA | 23072 |
rs114225408 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43278309 | GTGGTGTCATCCTTG[A/T]CTCATCCTTTCTCTG | 23072 |
rs114245669 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43228487 | GGTTGAAAATGTACC[A/G]TCAGGAGGTGCAAAG | 23072 |
rs114260198 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43447591 | CATGCACACGCTGGC[A/T]TGTGACTTCTTCCCA | 23072 |
rs114260230 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43483440 | TAGCATTACCCCAGT[A/G]AAGAACCATTATTTT | 23072 |
rs114289370 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43446237 | AAATGACTTTGTTTC[C/T]AATAAGAATCAAATC | 23072 |
rs114294668 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | HECW1 | GRCh38.p7 | 7:43499899 | AAGGATCAGAATACA[C/T]GAGTTGTAGCTGACA | 23072 |
rs114306232 | snp | C/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43249064 | TGAGGAGACCAATCG[C/T]CTAGCGTGAGTCTTC | 23072 |
rs114309953 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43207302 | TCTGCCCACCTCAGC[C/T]ACCAAAGTGCTGGGA | 23072 |
rs114312325 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43188162 | TTTTCGTGGCTCACC[A/G]GTTTCTTCAGCCCCA | 23072 |
rs114333368 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43391504 | AAAATAGTGCGTATG[A/G]AAGAACTGGCTCTGT | 23072 |
rs114347347 | snp | A/G | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112495 | CGCGGGGGCGGGGGT[A/G]GGGGTGCGCGGAGGC | 23072 |
rs114348096 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43240036 | CTATAATTAGGAAAA[A/G]AAGTTTTTTTTAAAT | 23072 |
rs114348901 | snp | A/G | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522564 | AGCTATGGCCCTGGC[A/G]TGCTCTCACCTGCCC | 23072 |
rs114360424 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43279973 | ATCTTCTGAGACAGA[G/T]CATCTGCTGAAGACA | 23072 |
rs114364556 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517757 | CCTGGGTTCTTTCAC[A/G]AACACCTACAAGAGC | 23072 |
rs114368554 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | HECW1 | GRCh38.p7 | 7:43222908 | CACCTGTGCATTGGT[A/G]ACATACATTTTCATT | 23072 |
rs114372418 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43177508 | CCGTGCTGTCTTCCA[A/G]CCAGGGTTTGAGCCA | 23072 |
rs114405466 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43472176 | ATGGCGTATGAACAC[A/G]GAAACAGCCTCTAAA | 23072 |
rs114413078 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43453534 | ATGTCAAGAAGGAAA[C/T]TGAATGTGTGACTCT | 23072 |
rs114414308 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43431500 | TCTCCTTGCCTGCTA[A/G]TCTCCCCACCACTTT | 23072 |
rs114430080 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43180323 | CACAAAAAACTTCAG[A/G]ATTTTGAGTAATCAA | 23072 |
rs114436892 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43225162 | AGGGACTCACCCAGC[C/T]ATCAGATGGTGGCTG | 23072 |
rs114436924 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121945 | AGGAACAACCTAAGA[G/T]TTGAGAAGGTCTGCA | 23072 |
rs114438099 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43167719 | CCACCCATGTAGGTA[C/T]CTTCTAGCATTAAGT | 23072 |
rs114441483 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142743 | CACATTGGTTCTTTT[A/G]GCACTCCAGTTTCAG | 23072 |
rs114453824 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43326122 | TCTTGCTGTTTCTGC[A/G]TAGGACCAGAGGGGC | 23072 |
rs114456289 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | HECW1 | GRCh38.p7 | 7:43343446 | CTATGACAGACGTGT[A/G]TGATATTCCCTGCCC | 23072 |
rs114462235 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43282378 | CCTGTGATGCCATCC[A/G]GATGACAGGAGCTGG | 23072 |
rs114464515 | snp | C/T | 0.021333 | 0.101051 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146406 | CAAAATTGCCTCTGG[C/T]TGGGAACCACTAGAT | 23072 |
rs114466294 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162972 | AAGTTGCCTAAGGTC[A/C]CATGAGCAGTGAGCA | 23072 |
rs114481339 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377425 | CTGTGACCTCACCCT[A/G]CCCCCTCACAATAAT | 23072 |
rs114486478 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43329012 | TCCGTCCCTGCATGC[C/T]AAGGTTCTGGCATTA | 23072 |
rs114536772 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43472600 | TTAATTATATTAAAT[A/G]AATATTAATTAAATA | 23072 |
rs114555051 | snp | C/G | 0.0444908 | 0.142359 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43249191 | CCGGTACCTGGGTGT[C/G]ACTCCGCCACTAACA | 23072 |
rs114576340 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43467277 | CAGAGTGCTCTGGGG[A/G]CGCCAGGGAGCATTC | 23072 |
rs114579182 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43489071 | CTGTTTCAAAGCCTT[A/G]TTCATTTCTGGGTGA | 23072 |
rs114597662 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43206554 | TCATTTTTTAAGAGG[C/T]GTAATTAACTTTATG | 23072 |
rs114622028 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43174277 | ATCATTGCTACTGGA[A/G]GATCCATGGAGATCC | 23072 |
rs114629226 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43526608 | CTCTGGGTTCTGCCC[A/G]GAACACAATGGCATT | 23072 |
rs114634247 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43171135 | CTTAAAAATGAAAAC[A/T]TGAAAATAAGTGTGT | 23072 |
rs114639662 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43377643 | CACAGAAATAACATT[A/T]TTTTTCTCTTTGTGA | 23072 |
rs114666905 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43411602 | TCCTTTACTATGTTC[A/G]TGGAATTGTCTGTTT | 23072 |
rs114673732 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43205484 | TTTTCCTGTAGTGGG[A/G]TGGATGAAATCACTT | 23072 |
rs114695166 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43485794 | AGTGAGTGAGTGACT[G/T]TGAGGCCTAGGACAT | 23072 |
rs114695618 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43350452 | CAATTATTCCCCCAA[A/T]TGTTTTCCAGGCTTT | 23072 |
rs114711373 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248013 | AAGGAAAGAAAGAGA[A/G]AAAGAAGAAAGCAAG | 23072 |
rs114723285 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120465 | TTGTAATCTCCATTA[C/G]AGCAGGAACCTATTT | 23072 |
rs114731821 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | HECW1 | GRCh38.p7 | 7:43467395 | CGTGAGGAGGCCTGG[C/G]GGATAAGTCCAGGGT | 23072 |
rs114731912 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | HECW1 | GRCh38.p7 | 7:43420970 | ATTGAAATACAAAAT[A/G]CCAAGTAGAGGTAAG | 23072 |
rs114750648 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518213 | ATAAAAGAAAAGAAA[A/G]GCCGGGCACAGTGGC | 23072 |
rs114756844 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43189432 | CTGTTACAAAAGCTT[A/T]TTGGAAAATCATTAA | 23072 |
rs114759133 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43496384 | AAAAACAGAAGGCTC[A/G]CGATGACTATCAGAA | 23072 |
rs114766916 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43225490 | CAAAATAAAAAAACT[A/G]GAAACAACCTAAATG | 23072 |
rs114774767 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43334476 | AATATTGAAAAATCC[G/T]CCAACACCCACAAAA | 23072 |
rs114777912 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43316100 | CAGAGAAAATATATT[A/C]CTTGTTTCTTAGGTA | 23072 |
rs114781842 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HECW1 | GRCh38.p7 | 7:43274613 | CCCGGGTGTGCCCCA[A/G]ATAAACTCAGGAACG | 23072 |
rs114791885 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | HECW1 | GRCh38.p7 | 7:43293553 | TCGGCATGAAACAAC[A/C]TTAGGTTCCCTGTCT | 23072 |
rs114820057 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | HECW1 | GRCh38.p7 | 7:43472400 | GTCTGTTTCTTGTGG[A/C]AGGATTTTAAGCTTT | 23072 |
rs114828544 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43440286 | CACCTGTACTGGCTG[C/T]CTCCCTGCCCTGAGA | 23072 |
rs114839312 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43339326 | TACCTTCTTTCAATC[C/T]GGATATTTTCAGTCG | 23072 |
rs114845199 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157799 | CTCCTGAGCTCAAGC[A/G]GTGCACCTGTCTTGG | 23072 |
rs114863419 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43203980 | TTATAAATGGACTCT[C/T]TTTGTCTTACCTAAA | 23072 |
rs114868935 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43436263 | GCCCTTGATTAAGGG[A/G]ACTGTAACATTCAAT | 23072 |
rs114884521 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43271767 | ATTATTAAAATGGCC[A/G]TATTTCACAAAGCAA | 23072 |
rs114890149 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511040 | AAGAAGCTTTATAGA[C/T]GTGTCCGTTACACTT | 23072 |
rs114899336 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43369537 | TTTGCCTTTTTGGGA[A/G]AGAACACCTTAATCT | 23072 |
rs114900536 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43370013 | GTTTTTAGGGGGGAA[A/G]AATGCAACGGCCAAT | 23072 |
rs114937366 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43466289 | CTAAGGAAATGATGA[G/T]TCTTAACTGACATAC | 23072 |
rs114950790 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43393109 | TCTGTTAAACCATTT[G/T]CCAAGTATGCTCTGT | 23072 |
rs114953615 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43371444 | GCTCAGTTTTGCTGT[A/G]GACCTAAACCTGCTG | 23072 |
rs114961620 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43405615 | GTGGGGGTGGTGCTG[G/T]TCATGTGTGCATCTT | 23072 |
rs114966438 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43432132 | TGCACCCGGCCAGTT[A/G]TTTATTTTATTTCTT | 23072 |
rs114979625 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43185327 | CTTTACAATAAACTG[A/G]TAAACGTAAGTAAAG | 23072 |
rs114987395 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | HECW1 | GRCh38.p7 | 7:43397599 | TTTGTGGGCAGCGGG[G/T]GGATCTCACCAAGTA | 23072 |
rs114993843 | snp | A/G | 0.030665 | 0.119967 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155553 | TATTTTACTTTGGCA[A/G]AAGAATTTTATATAT | 23072 |
rs114996694 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43326656 | GAAACAGGGCAGGAT[C/T]GTACATCCACCTTTT | 23072 |
rs114999057 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | HECW1 | GRCh38.p7 | 7:43283935 | CTGCGGCTGCCTTGA[A/G]TGTCAGGAGTGGAAC | 23072 |
rs115049421 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | HECW1 | GRCh38.p7 | 7:43542939 | AGTACGTCATACATA[C/T]GTCAGGGATTTCTGC | 23072 |
rs115055777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43495562 | CTTTGTGCCCACTCT[G/T]CCCCTTACAACCTGG | 23072 |
rs115059231 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43448611 | GGTTCTTCCAGGCAG[A/G]CAAGCAGTGAGGGTA | 23072 |
rs115077266 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | HECW1 | GRCh38.p7 | 7:43485803 | GTGACTGTGAGGCCT[A/G]GGACATTACTGTACA | 23072 |
rs115088111 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43399370 | TTTCAACTCACTAAT[G/T]TTGTACTTCTAAGGC | 23072 |
rs115094807 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43402148 | TCACCATCCTTCAGG[G/T]CGGTGTGTGATCTGA | 23072 |
rs115096753 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43379735 | TTCACTCCCTCCCCC[C/T]ATTTAGATCGTTTTC | 23072 |
rs115098387 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43222196 | AAAGCTCTCCAGGAA[A/G]ACCACTGAGGTAAGC | 23072 |
rs115102836 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43426539 | TGCAGCTAATTTTAT[C/T]TGGGATTTCTGTAAT | 23072 |
rs115113374 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | HECW1 | GRCh38.p7 | 7:43540899 | GGTCCTCATTCTCCA[C/T]GGTCTGAAAAAGGTT | 23072 |
rs115114705 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43345789 | GTTGTGTAGTATTCC[A/T]TCATATATATACACA | 23072 |
rs115118985 | snp | C/T | 0.00589633 | 0.0539759 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43466568 | GCTACATGCCAATTA[C/T]GTGAGTGCCCTAAAA | 23072 |
rs115127498 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43558853 | CTGGAGCAGGTGGAG[C/T]GGTATGGGCTTCTGG | 23072 |
rs115131637 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43304057 | GTTTCCCTTAACAGT[C/T]GTGACTCAGAGGAAA | 23072 |
rs115143420 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43277430 | GCCATGGTTTTTCGT[C/T]TCTGTCTGTACTGAT | 23072 |
rs115145952 | snp | A/T | 0.029116 | 0.117091 | intron-variant | HECW1 | GRCh38.p7 | 7:43255101 | TAGAACACAAACTCT[A/T]TGTTATTTAAGAATT | 23072 |
rs115165186 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43404088 | AAAGAGTTAAATTGG[C/T]TTACTCAAAGTTACA | 23072 |
rs115179107 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121964 | AGAAGGTCTGCATTT[C/T]GTTGCTTCTAGAATG | 23072 |
rs115198982 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | HECW1 | GRCh38.p7 | 7:43533283 | TAACCCATGCAAGTC[C/T]TGGTCCATTACCAGG | 23072 |
rs115202545 | snp | A/G | 0.0333695 | 0.124785 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112254 | AATGTGTCTCTGAGC[A/G]TTCTTAACTGTGTGT | 23072 |
rs115210744 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43407313 | CCTATTTTTTTAATG[C/T]CTCCACCTTGCAGAG | 23072 |
rs115218161 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43371224 | CTATGATGGTGGCTA[C/T]ATGTTATTATACATT | 23072 |
rs115234124 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43361757 | TGACCAACTGGGGAG[G/T]CTGGACAGAAACCAG | 23072 |
rs115246063 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43461801 | AGGAAATGCCTTGCA[A/G]TAACCACTACAGGCA | 23072 |
rs115272747 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | HECW1 | GRCh38.p7 | 7:43250593 | AGAGAGCGCCAGGAA[C/T]GTCCTGTGTGTACCT | 23072 |
rs115277045 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43290526 | AACTCCAGAAGGGAG[G/T]GGGTATAACGAGGCA | 23072 |
rs115278990 | snp | C/G | 0.0399052 | 0.1355 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43249392 | GCTGCCAGCACAAAT[C/G]AAGGTCCTGGCCATT | 23072 |
rs115288208 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43371366 | CTCTTATGTGGAACG[C/T]TGGTAGTTGGGGAGG | 23072 |
rs115296817 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123795 | CATAGCCCTTCCAAC[C/T]GGGTGGGCTGTGGGC | 23072 |
rs115301514 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43560734 | AGGGATCTTGTAATG[A/G]AAAGAAGAGTTTAAT | 23072 |
rs115323772 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43166597 | GCTTTTCTTTACTAA[A/G]AAGATGTTTTGTTTA | 23072 |
rs115325089 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | HECW1 | GRCh38.p7 | 7:43347967 | TTCATCAAGGACATC[A/G]GTATGTAGTTTTCTT | 23072 |
rs115333441 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146485 | ATAATATTTTGAATT[A/G]ATAATAAGGAAATGA | 23072 |
rs115342919 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138497 | GGGGAGTTCATTGTC[A/G]TGTCCTTTCTTCCAC | 23072 |
rs115367579 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43174631 | ACTATTTCTCTCCTT[C/T]GCACTCAATCTTAGT | 23072 |
rs115384682 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43477280 | GGATCAATAATCATA[A/C]ATATTTTTCTAACTT | 23072 |
rs115412415 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43430612 | TTGTCTATAGCTGAC[A/T]GGTTTAATTTTGCTG | 23072 |
rs115420013 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43561593 | TGTAGTTGGTTTGCT[G/T]GCAAATGCAAACAAC | 23072 |
rs115434129 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43492369 | TCTGTCCTTTTCCCC[C/T]CTCCCTTCCTCCTCA | 23072 |
rs115435932 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517011 | TCTTTTGAGACCGCC[A/G]TTGTATATGTGGTCT | 23072 |
rs115441865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43555785 | GCTTCACCCACTCAG[C/T]TCAGCAGACCCTCAG | 23072 |
rs115446152 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | HECW1 | GRCh38.p7 | 7:43478796 | CTATAATAAAAAAGA[A/G]CATTTATCTTAAATA | 23072 |
rs115453281 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | HECW1 | GRCh38.p7 | 7:43384605 | ATTTTAAAGCAAGTC[A/G]GTGAGGGGGAAAACG | 23072 |
rs115454867 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141787 | ACAGGTGTGAACCAC[C/T]GCACCCGGTGAGATA | 23072 |
rs115459170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43453490 | CTTGGTTTCGATCAT[C/T]CTGTGTTTGAGATGT | 23072 |
rs115465926 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43381464 | GTAGCTAGGACTACA[A/G]GCACATGCTACCATG | 23072 |
rs115477438 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511565 | AAATTTCTGAGCAAG[A/G]GAAACTGGTTTTCTT | 23072 |
rs115496254 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43167673 | GATGAGGGATTGTGG[C/T]GTAAAAGCCAAACCT | 23072 |
rs115499073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296134 | ATCACATAAGAGGAA[A/T]TCTTCTACTATAATA | 23072 |
rs115509549 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43260062 | AAAATATAAAAGCAA[C/T]CACAGGAAAAAATGA | 23072 |
rs115519375 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43493559 | TTGAGCAGCCGTGTT[C/T]GAAAATAAAAAAGCA | 23072 |
rs115519895 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | HECW1 | GRCh38.p7 | 7:43357716 | ATATGTTTTTATATA[A/T]TTATATGTATTTATA | 23072 |
rs115530424 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563332 | GAAATAAACCCAACC[A/G]TAATGGTCATTTGCT | 23072 |
rs115570665 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43194238 | TGGCTTGGAATTCTA[C/T]TTTTTTGGTTTATAA | 23072 |
rs115576122 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | HECW1 | GRCh38.p7 | 7:43467589 | TTCTCTGGCAGAGTG[C/T]CGGGGAGAGACTGAG | 23072 |
rs115597954 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | HECW1 | GRCh38.p7 | 7:43527448 | GGCTGCATCACTCCA[A/G]TCTCTGCCTCTGTCT | 23072 |
rs115602000 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143591 | GTGCCCAGCTGGATG[C/T]CTCCTTTAGATGCCA | 23072 |
rs115616739 | snp | C/T | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43439090 | ATGGAGCTGCAGTCA[C/T]GTGTCACATGCAGTG | 23072 |
rs115624289 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43199701 | ACAATTGATTACACA[C/T]GTTATATATTTTTAG | 23072 |
rs115630533 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43532426 | TCCAAAGACCCTACA[C/T]GAAACTTCCAATGGA | 23072 |
rs115640762 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | HECW1 | GRCh38.p7 | 7:43535768 | TGCTCTCACCAACTG[A/G]TAATCAGGGGAAGAG | 23072 |
rs115646220 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43395434 | CTTTAAGACAAATGT[A/G]AGTTTCAAGTTTTCA | 23072 |
rs115649153 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | HECW1 | GRCh38.p7 | 7:43558039 | AGAATGTCCATCCAC[A/G]TCACAGCGTGTGGGG | 23072 |
rs115679404 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43390447 | CCAGGAGTCTGAGGT[A/G]GGAGGACCACTTGAG | 23072 |
rs115688685 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43330924 | ATGACAGTGGCTCTG[A/G]GAAGGTAACCAAATG | 23072 |
rs115702617 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316769 | TCTCCCCTCCCCTTT[C/T]CTCTCCTCCCCTCCC | 23072 |
rs115706196 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43199860 | AATTCTATATATACA[A/C/T]GTTTGGTTTGTTGTT | 23072 |
rs115720828 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43185488 | GGACTGAGCCGTCAA[C/T]CTGTGAGATCTGATG | 23072 |
rs115723292 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43271779 | GCCGTATTTCACAAA[A/G]CAATCCACAGATACA | 23072 |
rs115734438 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | HECW1 | GRCh38.p7 | 7:43288216 | AATGAGAAGAGGAGG[A/G]GAATTAGCTGGACAT | 23072 |
rs115740528 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43212561 | TACAGAAGGGAGGCC[A/C]AGGCTATTACGCTGC | 23072 |
rs115755846 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151648 | AAATACCAAATAAAC[A/C]TTGCTAAAAATTGAA | 23072 |
rs115809282 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43538095 | TTGATCCGGTGGGCA[C/T]CCAACCTGAGTTAGA | 23072 |
rs115854594 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HECW1 | GRCh38.p7 | 7:43347050 | GGTGGTATTCTGAAG[A/G]GGATTGCATTGAATT | 23072 |
rs115859261 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43317028 | ATCTTAGGCAGTTTA[C/T]TTAATCATTCACTAC | 23072 |
rs115861085 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296517 | CTTGGCGGCGCAGCT[G/T]TGGACGCAGCTGCGG | 23072 |
rs115864090 | snp | C/T | 0.030278 | 0.119257 | intron-variant | HECW1 | GRCh38.p7 | 7:43451024 | ATCTAAAGTCTTTCC[C/T]GACTCCGTGCCTTAC | 23072 |
rs115869245 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299552 | TTAAAAAAAAAAGTT[C/T]CCAAACTGCCTCAAT | 23072 |
rs115910874 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43226790 | TGCTGCCCTCCGAAG[A/G]GCCTGGCGTCTCCCG | 23072 |
rs115918351 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123857 | TCTCCAGAAGTCTGT[A/G]TCCTGCTCTCAGTTA | 23072 |
rs115922385 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43252524 | TTAAGTTGGGAACAC[C/G]CTGGCTTATACCATG | 23072 |
rs115925863 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162829 | TGGAGCACTTGTTCT[A/G]TGGGAGGCATTGTTC | 23072 |
rs115936273 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510705 | TAGGGGGTCAGGGAG[G/T]GGGGAGTGGAGTCTG | 23072 |
rs115938855 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524351 | AGTTAGAAAATATGA[A/G]AAGACCAAACCTGAA | 23072 |
rs115961546 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43489842 | ATTTGCCCTACATTA[C/T]GATCTGCAATATCAC | 23072 |
rs115976850 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297122 | CATCTCATGCATTCA[A/G]CTTTTTCTGCCTCAT | 23072 |
rs115985855 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43271510 | ACGATTTTAGCAAGG[G/T]TGTAGGGTACAAAAT | 23072 |
rs116002791 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43356061 | TCCTTACTTATCAAT[A/T]ATAATAACAAATATA | 23072 |
rs116004786 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43373735 | CATCACCGTCTATCT[C/T]CAGGACTTTTCATCT | 23072 |
rs116008304 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43532143 | CAGTAAATGGCACCC[A/G]GTTGCTCTGGCCCAA | 23072 |
rs116012852 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43535698 | CGAGGGTGTCCGTAC[C/T]GTACCGTGGTGGGAA | 23072 |
rs116013190 | snp | A/C | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43438225 | CCTGTAGGCTGCAAT[A/C]GTATAGTCTCACAGA | 23072 |
rs116016393 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43526706 | ATTATCCAGTTAGAT[A/G]AAGATATAGCAGGGC | 23072 |
rs116018417 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43204183 | AAAGCAGCTAATTTT[A/G]TTGCTCCATCATTGT | 23072 |
rs116048550 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198998 | TAAGCTAAACCATTT[C/G]CCTTCCCAGTTCCAA | 23072 |
rs116051311 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43396192 | CTAAATATTGAGCAA[A/T]GATGAAAAACAAAAC | 23072 |
rs116053986 | snp | C/T | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377190 | AGCCCAGGCCCATCT[C/T]CTCCTCCATACCAAC | 23072 |
rs116064652 | snp | C/T | 0.0599851 | 0.162463 | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163511 | CCTCCCTAGGCTCCC[C/T]GACCTTCCATTTGAA | 23072 |
rs116067364 | snp | A/T | 0.116838 | 0.211584 | intron-variant | HECW1 | GRCh38.p7 | 7:43286689 | CCACCCCCCCAAAGG[A/T]GTTTGGGAGGAGGGA | 23072 |
rs116072623 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43556027 | GCTGAGCTACAACCA[C/T]ACACCTGCCCGTGGG | 23072 |
rs116098279 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120493 | TTTGTTTACCCAGTG[C/T]CTGGAAAAGTGTCTG | 23072 |
rs116101565 | snp | C/T | 0.030665 | 0.119967 | intron-variant | HECW1 | GRCh38.p7 | 7:43250728 | GCAAGTTTATTTTAT[C/T]TGGCTGCCGGTGCTT | 23072 |
rs116113442 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43467524 | GCAGCAGGCCACAGG[A/T]ACCAAGAGTAGCACT | 23072 |
rs116117333 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43261966 | TGGTTTATGCCTGTA[A/G]TCCCAGCTCTGTGTG | 23072 |
rs116131626 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43440873 | TGGCTTATCAAAGAA[A/C]AATTTTTAAGTCGGG | 23072 |
rs116138059 | snp | A/G | 0.0410537 | 0.137264 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524239 | TTCAAAGAGTGTGAG[A/G]AAAAAAGCTGGCTGT | 23072 |
rs116149707 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43279492 | TCTAGAGCCTAACCC[A/G]ACCATCCACGCTCTT | 23072 |
rs116152633 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43344816 | CTATTCATTGAGTTC[A/G]CTATTTCAAAGTACA | 23072 |
rs116155162 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269605 | CTGGAGGAAATAAAC[A/G]AATTGAAAGGCAAGA | 23072 |
rs116169570 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126169 | GAGTCTCCTTGGATT[A/C]TTAGGGATTGCTCCT | 23072 |
rs116171402 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43164800 | AGTGCAGACTCTTCC[A/G]GAATTAGAAAGGAGA | 23072 |
rs116173284 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43220830 | AAAGGAGAGAAGGGA[A/G]ACCAGTTTCTTGTGA | 23072 |
rs116182372 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43293497 | TTTTGTTACTTAAGC[A/T]TGGAAAGTTAGGGTT | 23072 |
rs116196530 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137169 | TGGGTTCAATCGCTT[C/T]ATGTCTGAATCACCG | 23072 |
rs116199058 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43173047 | TCCGCGTTCAGACAC[C/T]CAACTCCTTAAAGCT | 23072 |
rs116220501 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359163 | ACTACTGTAATATTC[A/G]TATCTACAGCATTGA | 23072 |
rs116227494 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43486652 | GTGACAGCTATGACA[A/T]GACCAGTGATAGGAC | 23072 |
rs116236606 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43327657 | TTAAAATCCCAAAAG[A/G]ATTAATCTTGCTAGA | 23072 |
rs116247620 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43354351 | AATGAGACAGCAATA[C/T]GTGTACTCTCTAACA | 23072 |
rs116248036 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43387799 | CAGTTATGTGACCTC[A/G]TGGGCCCCTTGATTG | 23072 |
rs116258187 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43190633 | CTTTCTATGCTCTCT[A/C]CAAGGACCAGAGCTT | 23072 |
rs116284161 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | HECW1 | GRCh38.p7 | 7:43555783 | TGGCTTCACCCACTC[A/G]GTTCAGCAGACCCTC | 23072 |
rs116297481 | snp | A/C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376409 | GGGGTAGCCAGCCAG[A/C/T]GTCTGGGCTATGTGG | 23072 |
rs116299562 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300842 | TGGAAAAGCAGGTAC[A/G]ATGACCTCCCACACT | 23072 |
rs116324335 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HECW1 | GRCh38.p7 | 7:43219300 | AAGACCCAGGGCTTT[C/T]CTACTGGACAAGAAA | 23072 |
rs116344045 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43493911 | TCCCAAATGGGGGTC[A/C]CAAAGTGGGCATGGT | 23072 |
rs116362260 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | HECW1 | GRCh38.p7 | 7:43425127 | AATGGCAAAGCCATA[A/G]AGCCATAGCAATGGA | 23072 |
rs116393582 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43337743 | TCTCCCAAGAGGCAA[C/T]AATTCCAGCAAATTC | 23072 |
rs116399196 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43215522 | CCTTTTTAACCAAAG[A/G]TTAAATCGTTAACAA | 23072 |
rs116403192 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | HECW1 | GRCh38.p7 | 7:43409728 | AGGCTGAGGATAACT[G/T]ATGTCCCAAGTTAAA | 23072 |
rs116406567 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | HECW1 | GRCh38.p7 | 7:43331782 | TGAGCATCATGGCAG[C/T]TTGCCTAAGGTTCAG | 23072 |
rs116410508 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43548343 | CCAAAAAAATTCCCA[A/G]TATATTTATTGAAAA | 23072 |
rs116424138 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43278402 | TCCGCAGCTCCCACC[C/G]TGGTTCTAGCAAGCG | 23072 |
rs116438608 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43538087 | GCTCATGATTGATCC[A/G]GTGGGCATCCAACCT | 23072 |
rs116443238 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43475039 | TGGGAAGGTGAAAAA[C/G]TGCTGGGGAAGGAGA | 23072 |
rs116445171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123161 | CTATTTTGTACCAGA[C/T]GCTGGGCTGGGGGCC | 23072 |
rs116454093 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | HECW1 | GRCh38.p7 | 7:43320817 | TTCATTATTTGTTCC[C/T]GTTGCACTGCCTCCA | 23072 |
rs116464379 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43421469 | AAATTAAGAACCACC[A/G]TTCATCAAAACTTTA | 23072 |
rs116466808 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43340073 | AACCTCTCATCTAGA[A/C]GTTTTAGTCCTATCT | 23072 |
rs116475133 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43230667 | ATGGGAGCATCCTGT[C/G]AACAGATTACTCTTG | 23072 |
rs116480289 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162241 | CTGCCGTAACAAATT[A/G]CGACAAACTTGTGGC | 23072 |
rs116486179 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43223971 | CAACCCTTTCAACAG[A/C]CTCCCATCCCCTCTT | 23072 |
rs116490138 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120492 | ATTTGTTTACCCAGT[G/T]CCTGGAAAAGTGTCT | 23072 |
rs116491585 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43184629 | CCCTCAACTTCTGGG[A/G]AGCAGAGACGGGCTA | 23072 |
rs116492297 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43291220 | CTAGCAGTCTTGCTA[C/T]GAGAGTACACTGAAC | 23072 |
rs116497914 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | HECW1 | GRCh38.p7 | 7:43550311 | TAGCAAGGAAAAAAG[A/C]CTCCAGGGATAATAA | 23072 |
rs116520269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43453157 | AAGTTTGCCCAAGTT[A/G]CTGTGTAGGGAATAA | 23072 |
rs116522052 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43405049 | AATCTCATCTCTGAT[A/G]TCAACCAGCCCTGAC | 23072 |
rs116542763 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43244901 | GGAGAGGGACGCCCT[C/G]AGATGTTCAGTGTGT | 23072 |
rs116563002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163270 | GATTCATTACTAGTT[C/T]GAGGATTGCAAATAC | 23072 |
rs116564151 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | HECW1 | GRCh38.p7 | 7:43446305 | GTTTTAACCAAAGAT[C/G]TTCTTTCTTAGTCAT | 23072 |
rs116567951 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43270240 | AGCAGCTTGGCTGGC[A/G]GGTTTAGACTTCGGA | 23072 |
rs116571450 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124578 | AAGAGGAACCTGTCT[C/T]TGAGCTTGGGGCCTC | 23072 |
rs116574021 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | HECW1 | GRCh38.p7 | 7:43185404 | GAGGGGTAAATAGTC[A/G]GAACTGTCTCAATTA | 23072 |
rs116580078 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | HECW1 | GRCh38.p7 | 7:43261498 | TGCAAGGCAGTTTAA[A/G]CCCTTGGGGGTTAAA | 23072 |
rs116582899 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152799 | TTCATATCTGTAGGC[A/G]TTTCCCCCTGAGCTG | 23072 |
rs116605843 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | HECW1 | GRCh38.p7 | 7:43229778 | TCTCTCCACAAGATA[C/T]TCATTATTTACAAAG | 23072 |
rs116607164 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43334169 | CTGAACATTGTGTGT[G/T]CCTTCCTGAGTACTT | 23072 |
rs116617191 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43410393 | TCCCATCGTGAGGAC[C/T]CTATCCTCATGACTC | 23072 |
rs116617760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405999 | CACCCCCCAGTCTTG[C/T]GCATGCCTCCTCTTC | 23072 |
rs116620227 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43395068 | TGTGGTGCCAGCTGA[A/T]CCATCAAGTGCAGGG | 23072 |
rs116621839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43407284 | AGGCCCACATATATC[A/G]TGAGACTACAACCCC | 23072 |
rs116629107 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | HECW1 | GRCh38.p7 | 7:43473448 | GAAAATGATAGTATA[A/G]AAAGGACTAGTGGTG | 23072 |
rs116631904 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | HECW1 | GRCh38.p7 | 7:43211004 | GCCGGCTGGAATGCC[C/T]GGGTTTGTATCCCGG | 23072 |
rs116634976 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148442 | CTCTGTGTCCTCATG[C/T]CCAAGCCATTCTGCC | 23072 |
rs116635252 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43289478 | GGGTTCCAGACTCTT[C/T]ATGAGACCTCCCTGA | 23072 |
rs116636467 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43284286 | GTTTTGAAATATGTG[G/T]GCATTGTAGAATGGC | 23072 |
rs116673665 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122679 | GGAAATTCACAAATT[A/G]TTATTTTCTCCTTTC | 23072 |
rs116676027 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43388000 | GCCATTCCGTTCTCA[A/G]GGGAACTCAGTGAGA | 23072 |
rs116681028 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43526356 | ATGGGAGCATGAGGG[C/T]CTTGTCTATTATGTT | 23072 |
rs116685665 | snp | G/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509724 | AGGTCTCCAGAAAGC[G/T]GCTGGGACACCTGGG | 23072 |
rs116688208 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43407792 | GGCTGACTGTGAACC[A/G]GCCCTCCTCCTTCCC | 23072 |
rs116698600 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43265763 | ACTTCAGGCATCAGC[C/T]GAAAACAGGGTTCCC | 23072 |
rs116699904 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43256074 | TGCTGCTCACCATCT[C/T]ACACACCATCTTCTA | 23072 |
rs116709805 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | HECW1 | GRCh38.p7 | 7:43327835 | GATATTATGCATCCT[A/G]TGTGCTAATGGGATG | 23072 |
rs116715643 | snp | A/G | 0.131723 | 0.220251 | intron-variant | HECW1 | GRCh38.p7 | 7:43504801 | TTTACCTCACTGAGA[A/G]GTTGAAGCCATCCAG | 23072 |
rs116727862 | snp | A/G | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43173926 | CTCACTGCAGACTAC[A/G]ACTCCTGGCTCATGT | 23072 |
rs116728831 | snp | A/G | 0.0592355 | 0.161582 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149804 | ACACTCATACAATAG[A/G]GTTTATTTAGACTTT | 23072 |
rs116729017 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43179848 | CATGATTGAGATTTA[C/T]TTATCACCATGTAAA | 23072 |
rs116734366 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517073 | TGCTTGTGCTAACAT[A/G]TATCATTTTAAGAAA | 23072 |
rs116735555 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43353445 | ATTTCCAAAAGGGTA[A/G]TATAGAGGCAAGATG | 23072 |
rs116752045 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43528760 | CACCAGGGCTAGACA[C/T]TCATTTCAGTTGCTA | 23072 |
rs116755382 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43561659 | TTCATTCTAGAGGAA[C/T]GTGGCTCTTTAGTGT | 23072 |
rs116771694 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43394069 | TTTAGCCATTGATTG[A/T]TAATTGTCCTGGTGG | 23072 |
rs116776274 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43409624 | CTCCCCAGCCCTCTG[C/T]TCTGGGCCACCTCCC | 23072 |
rs116790860 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43342120 | AAAAACCAGACTCAC[A/G]CCTGAAAAGCTTTAA | 23072 |
rs116794508 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | HECW1 | GRCh38.p7 | 7:43259690 | GTAAATAATGGATTG[A/G]ATAGGCTTAACAGCA | 23072 |
rs116805178 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43329795 | TGAAGTGAGGGTGTG[A/C]AGGACTTTGTGTAGG | 23072 |
rs116827430 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43166827 | CAGGACTGAGGGTGG[A/G]GCCAGGGAGGGCAGC | 23072 |
rs116832337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43405737 | GAGCCACTCGTACCC[A/G]TTCTGGGAAGGTAGG | 23072 |
rs116835837 | snp | A/T | 0.103082 | 0.202275 | intron-variant | HECW1 | GRCh38.p7 | 7:43336343 | GCTACTTAAAAAAAA[A/T]TTTTTTTTAGAGATG | 23072 |
rs116845526 | snp | C/T | 0.0689305 | 0.172377 | intron-variant, upstream-variant-2KB, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113661 | CAGGGAGGGAGCTGC[C/T]GGGGCGGGGAGGGGG | 23072 |
rs116846729 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315474 | ATTATTGTTATTATT[A/G]TTATTATTATTATTA | 23072 |
rs116847298 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43342729 | TCATTATTCTTAAGA[A/T]TGTTTATACATAGAG | 23072 |
rs116858275 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43526651 | TTCTCTGGTCTGTGC[A/C]GCTCAAATAATTAAG | 23072 |
rs116876905 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116692 | GGAAACCAGGAAGTT[A/G]CAATACCCACATGTC | 23072 |
rs116886313 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43422691 | GATACTTCTTGATGC[C/T]GAGTGCTTTACCAGA | 23072 |
rs116901848 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131368 | GAAGTGTTTCTATGG[C/T]TTGACCAGCTCACAC | 23072 |
rs116904165 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43187902 | GTCCCAGACTGAATT[C/T]TTTCACATGTGCAAC | 23072 |
rs116904283 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43189777 | CAATGGAAGTTGATA[A/T]CAAGACTCTTGGCAA | 23072 |
rs116904922 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158227 | GGCAATACAGGTTGA[C/T]CAATATGGGTGGTTA | 23072 |
rs116906991 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43233189 | CATATATATTCAATG[C/T]AGAAACAACAGTTAC | 23072 |
rs116911703 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43496454 | AAAGAGCAAGAACTT[G/T]TTCTTCAGGAGGTCA | 23072 |
rs116914041 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43312911 | ACAAGAGTCAACAGA[C/T]TCAACACCGGGTCAT | 23072 |
rs116914273 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43480625 | TTTGTGTGTGTGTGC[A/G]TGTGTGTGTGTGTAC | 23072 |
rs116919090 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43216706 | TTCCCCCAGGCTGGA[G/T]TACAGTGACGTGAAC | 23072 |
rs116923536 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137643 | CAACCCACACCTCCT[A/G]GGCTCAGGTGATCCT | 23072 |
rs116937961 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | HECW1 | GRCh38.p7 | 7:43484779 | ATACATAAAAAGATC[A/G]TTATTTGACACTTTC | 23072 |
rs116945469 | snp | A/C/T | 0.0167069 | 0.0898595 | missense | HECW1 | GRCh38.p7 | 7:43501242 | AGATTATGTCCTACG[A/C/T]CCCCCTGCAGGCTGC | 23072 |
rs116948973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43543284 | GACAGTGCACTGGGT[C/T]GCTGCATGAGAATGA | 23072 |
rs116954804 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | HECW1 | GRCh38.p7 | 7:43391178 | ATAGATTAAAAGAAG[C/T]TAATCACTTACATCT | 23072 |
rs116965220 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | HECW1 | GRCh38.p7 | 7:43427755 | TCCAAGATCATTCAG[A/G]TTGTTGGCAGAATTG | 23072 |
rs116987435 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43530684 | TTTATTATCAAAATA[C/T]CTACTAGACATCTCC | 23072 |
rs116992184 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43361379 | ATTTCTTTTAGTCTT[A/G]TAAATAAATTAATGG | 23072 |
rs116997114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43199099 | ACCCTCATTGCACAC[C/T]CTCTCTCTCCACGGT | 23072 |
rs116997906 | snp | A/G | 0.245631 | 0.249962 | intron-variant | HECW1 | GRCh38.p7 | 7:43440092 | CCCACCGTGGTTAGG[A/G]GCAGAGTGTTGGGGT | 23072 |
rs117039808 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154413 | GCTTTATCTGTCAAA[A/G]ACAAAATAAATTATG | 23072 |
rs117057570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43177992 | TGATCTCCCCTGCCC[C/T]TGTGGGCAGGGTTTT | 23072 |
rs117078656 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43487699 | ATGGTGGCTCACACC[A/T]GTAATCCCAGCACTT | 23072 |
rs117079085 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43456947 | TGTCTCATAAATCAC[C/T]GTATGCATTCCTACC | 23072 |
rs117083950 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43480872 | TCTCAAGGGAAGAGC[C/T]TATTGTTGATGTATC | 23072 |
rs117090826 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43232627 | ACATGATGTTCTTGC[A/G]GGAAAAGGGGCAGTA | 23072 |
rs117096403 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43236954 | GTGATTTGGGGGTCC[C/T]GAGATTTATTTTCCT | 23072 |
rs117096990 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296960 | CAACCACCAATTAGA[A/G]ACAGTGATGGCCTCC | 23072 |
rs117123592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43211371 | TCACCTTTCTCCTCC[A/G]TGAATGAATGAAACG | 23072 |
rs117144536 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43235192 | GGGACCCTGCAGGAA[A/G]AAGTGGAGTTCCCCG | 23072 |
rs117148654 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43304356 | AATTCTGGGCACCAA[A/G]CCTAGTGCTTACAAG | 23072 |
rs117156413 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43389833 | AGAAAGAGTCTCACA[A/G]TGTTGCTCAGGCTGA | 23072 |
rs117181921 | snp | C/T | 0.251859 | 0.249993 | intron-variant | HECW1 | GRCh38.p7 | 7:43440087 | GGTGTCCCACCGTGG[C/T]TAGGAGCAGAGTGTT | 23072 |
rs117182030 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43475914 | AAATATGTTTTCGTG[A/T]CCTAATAAAGCCTCC | 23072 |
rs117194363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43473725 | CGGGATCATTTAAAA[A/T]ACAAAGGTTAAATAT | 23072 |
rs117200234 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43505279 | ATCTGAAACCCACCT[C/T]TCCTCCACTACCTGT | 23072 |
rs117213090 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43266150 | CCCAAGGTCAAGGGG[A/C/T]GGGCTAAAAATTTCC | 23072 |
rs117225727 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43449306 | CAATGAACTGGGTGC[C/T]GGCATGAGGGGAACC | 23072 |
rs117236982 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516057 | ACTCAATTTAAAATA[A/G]TGCATCCATTTATAA | 23072 |
rs117244982 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43480670 | GTGTATATATATACA[C/T]ACACATATATACGCA | 23072 |
rs117250149 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43398501 | CAGGCATGAAGTACA[C/T]GTGCCTCCTTGGGAG | 23072 |
rs117271644 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | HECW1 | GRCh38.p7 | 7:43429468 | ATGACCAGACTCCAA[A/G]GGCACCACTTCTTAA | 23072 |
rs117280168 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514824 | ATGTTATTATTACAA[C/T]ATTATAACCCACATA | 23072 |
rs117281915 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43306094 | TAGAGACGAGGTTTC[A/G]CCATGTTGCCCAAGC | 23072 |
rs117285069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43461632 | CCTCAGCAGAGAGAA[A/G]ATCACAGAGTGCCAT | 23072 |
rs117288661 | snp | C/T | 0.165527 | 0.235296 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510832 | TCAAGCATGTTTCAG[C/T]GCAGCCACAAAATAA | 23072 |
rs117289661 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | HECW1 | GRCh38.p7 | 7:43408798 | GGGAGGGGAGGCCTA[A/G]GTCATGAGAGTGGAT | 23072 |
rs117290362 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43500976 | TGCAATTGAGCTAGC[A/C]AGAGCTGCGTAAAGT | 23072 |
rs117318664 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43365959 | ATAAAATAATATTAG[C/T]CAGCATGGTGGTGCA | 23072 |
rs117323658 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43479248 | GGGGGTAACGAGAGA[C/T]GGTGACAGATCATCA | 23072 |
rs117327935 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43181696 | TTTGGGTTCTTTGCT[A/G]TTGAGTTGTTTGAGT | 23072 |
rs117328290 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43405142 | TGTGTTCAGGATTAA[A/G]TCAGAAAATGTATTT | 23072 |
rs117337377 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43179165 | AGGTTCTTGCTTTCC[A/G]CAGAAAATAATAAAT | 23072 |
rs117341104 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43394550 | TTGGGGTTTATATAT[C/G]AGGGAAGGAATGTAA | 23072 |
rs117344169 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43285205 | AACAGGTTGTTGTGA[A/G]AGCTTCCTGGGATTA | 23072 |
rs117347267 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43351175 | TCTACCTGCCTCCAG[A/G]CTGTTACTGGGGGTT | 23072 |
rs117363274 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43267583 | GAAAGAAAAATTAAA[C/T]AACTAAAATATAAGA | 23072 |
rs117363576 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158245 | ATATGGGTGGTTATT[A/G]TACATAAACCATAAA | 23072 |
rs117363600 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43477995 | AAGTTGTCTTATGGT[A/C]CAAAGGGTTTTGTTG | 23072 |
rs117365583 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43441792 | ACATGCTACAAAATG[A/T]TACTCTTCTTTTATT | 23072 |
rs117372020 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43394666 | AGTTTCAGTCCCTCA[C/T]CTGAGAGTCAGTTTC | 23072 |
rs117395233 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43475061 | GGAAGGAGAGTGGTG[A/G]TGGTTGCACAACCGT | 23072 |
rs117407647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43476803 | GGTAAAGATTTAGTG[C/T]TAACGATTAACTCAC | 23072 |
rs117422163 | snp | A/G | 0.251859 | 0.249993 | intron-variant | HECW1 | GRCh38.p7 | 7:43440096 | CCGTGGTTAGGAGCA[A/G]AGTGTTGGGGTGATG | 23072 |
rs117445746 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562289 | CCATTTCTATCATTG[A/G]AGGGAAAATGTGAGC | 23072 |
rs117453545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268447 | GTGATTTTGTCCCCC[A/G]CGGACATTTGGCAAT | 23072 |
rs117486174 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43246787 | GCAAGAGAGAACTAA[A/C]GTTTGTGACAGGGAA | 23072 |
rs117499899 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43234629 | GAGACCCAGGGAAAC[A/C]TTCATCTCCTACCCA | 23072 |
rs117519826 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43357385 | TAGTATTCAGTCACA[A/G]AAAAGAATGGAATTC | 23072 |
rs117541300 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146865 | TGCTTATCCCAGAAT[A/G]TGTGGACATGAAGAA | 23072 |
rs117551526 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | HECW1 | GRCh38.p7 | 7:43170575 | CGGAAGGGACAGCAC[A/G]CTCTCACTGGCAGAG | 23072 |
rs117557838 | snp | A/G | 0.0167143 | 0.0898765 | missense | HECW1 | GRCh38.p7 | 7:43501241 | GAGATTATGTCCTAC[A/G]TCCCCCTGCAGGCTG | 23072 |
rs117559544 | snp | G/T | 0.171704 | 0.237423 | intron-variant | HECW1 | GRCh38.p7 | 7:43336084 | TCCCCTCCCTTTCTT[G/T]CTTTCTCTTTCTTTC | 23072 |
rs117561875 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43455706 | CGTCACACCATCACA[C/T]CATCACGGGTGTGAT | 23072 |
rs117566442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43534580 | GACCTACTGCAGCTA[C/T]TGGAAATTTGAGCAA | 23072 |
rs117572560 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43277837 | CCATTTTCAGCCCTC[A/G]TCTTCTGTGCTGGAC | 23072 |
rs117574423 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43449003 | GTCACATCATTGCAT[G/T]TGCTTGGGGTTCACA | 23072 |
rs117592032 | snp | A/G | 0.245631 | 0.249962 | intron-variant | HECW1 | GRCh38.p7 | 7:43440089 | TGTCCCACCGTGGTT[A/G]GGAGCAGAGTGTTGG | 23072 |
rs117600440 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43561625 | CATTTTTAGTTATTC[A/C]ATTCCTTCCACCAGT | 23072 |
rs117614086 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43435441 | TTCTTAGGAGTTATA[C/T]AGGAGTTAACTAAAA | 23072 |
rs117618809 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110978 | GCAACTCCTCAGGGG[A/C]GGATAAAGCACACCA | 23072 |
rs117618914 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43553792 | CTGTTGCCTGCATAT[C/T]TCCTCCTCTTTCTTG | 23072 |
rs117623466 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43500983 | GAGCTAGCAAGAGCT[G/T]CGTAAAGTACTTGAT | 23072 |
rs117648218 | snp | A/G | 0.039522 | 0.134904 | intron-variant | HECW1 | GRCh38.p7 | 7:43166303 | GGCCAGGTTGGTCAC[A/G]AACTCCTGACCTCAG | 23072 |
rs117663548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43239211 | CTAGTGAAACTCTTC[A/T]TCCCACCTCTTGGGC | 23072 |
rs117667731 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43440010 | GCAGAGCAGCTCCTC[C/T]TCCAAAGCCTTCTGC | 23072 |
rs117671241 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125402 | AGAATGAAAAGTAGC[A/G]GGTAGAAGATTTTGA | 23072 |
rs117672588 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43499296 | TCAAAAAAATAAAAA[A/C]TTTTTTAAAGAAAAT | 23072 |
rs117685646 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111064 | CCATGATGGATAGAA[C/T]AGAGAGCAAACATCT | 23072 |
rs117689113 | snp | C/T | 0.176861 | 0.239062 | intron-variant | HECW1 | GRCh38.p7 | 7:43507018 | GAAGTTGCGGTAAGC[C/T]GAGAGCACACCACTG | 23072 |
rs117691007 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43556478 | GATAGCTTGCGCCCA[A/G]GAGTTCAAGACCAAC | 23072 |
rs117694515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43197726 | TTGCTGGGCAGGTGG[A/G]GGACTCTGACGAACA | 23072 |
rs117696180 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132082 | CTATTTTCTCTGACT[C/G]TTAGTGAAAGGATCA | 23072 |
rs117698523 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43412192 | TGAGTTAATTTTGTA[A/C]CACTTTACATAAAAT | 23072 |
rs117707164 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43349674 | TATATAATAATAGCT[A/G]CCCCTGCTCACTTTT | 23072 |
rs117714282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43180088 | CGTTATCTGCCCTTA[A/G]CAGAGTTGGTAACAT | 23072 |
rs117714835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43364152 | ACAATACGCTAAACC[A/T]ACCATTCTTTGAAAA | 23072 |
rs117737329 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160992 | GGTTTTTTTTTTCTC[C/T]TTCTAAACCATCAGC | 23072 |
rs117742841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43454390 | TTTACTAATATTAGT[C/T]TGGGATCCATTAAAA | 23072 |
rs117749707 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133153 | TACAGCCTTCAAATA[C/T]ACCCAACCTGAGCAC | 23072 |
rs117761301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43336919 | TTCCATGGTGTATAT[A/G]TACATTTTCTTTATC | 23072 |
rs117768391 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | HECW1 | GRCh38.p7 | 7:43498170 | GACAGAGGATATAAT[A/G]TCTGGTGGAGAGCCA | 23072 |
rs117778044 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43377827 | TGATCCTGGGGACTT[C/T]CTTATGCCTCCCCCA | 23072 |
rs117789459 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43381942 | GTGCTCTGATTACAG[G/T]TGTGAGTCACCACAC | 23072 |
rs117789947 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43479351 | CTATGAGAATCTAAT[A/G]GCACCACTGATCTGA | 23072 |
rs117797320 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43270385 | GAAACTGTCAGATGG[A/G]GGTATCAGCTAGCAA | 23072 |
rs117812813 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | HECW1 | GRCh38.p7 | 7:43307929 | ATATACACACACACA[C/T]ATAGTGAAATGTATT | 23072 |
rs117814720 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43273160 | AACAGTAGAAACTGG[A/G]TTCTACTAGAAGGGG | 23072 |
rs117825357 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43342601 | TTCTAGATAACTCTT[C/G]AGGCTAACTCTTACA | 23072 |
rs117837357 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43526820 | ACCCTGGGCAACATA[A/G]CAAGACCTGTCTCTA | 23072 |
rs117865075 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43494202 | TGTATTTTCACTCTG[C/T]AAATTAGAGCCACTA | 23072 |
rs117865227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43441263 | GGATGGCATGAAAAT[C/T]CAGGGTGGAGACTTG | 23072 |
rs117869056 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43341392 | TCGTTTTGGTCACTT[C/T]TGCTATGCTATCGTA | 23072 |
rs117889829 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562481 | GCAAAGCTGAAATTT[G/T]TATACATTCAACTCA | 23072 |
rs117926516 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43536651 | CTTCAGATACAATGG[C/T]CCCCATGAGAAGCAG | 23072 |
rs117930106 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43405556 | CAGGGAAGCTTCTTA[A/G]AGACTTGAGACTGGG | 23072 |
rs117961191 | snp | A/T | 0.174932 | 0.238463 | intron-variant | HECW1 | GRCh38.p7 | 7:43347248 | GTTTTTTAAATTTTT[A/T]AAAATTTAATTTAAT | 23072 |
rs117984438 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137879 | TTATCACCTGTTTAG[A/G]TCTTACTCCCTCCCA | 23072 |
rs117991562 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43387264 | TCGAGGTTATGGAAA[C/T]GGATTCATCTTCACT | 23072 |
rs117994403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244376 | GGGAGGCTGATGGCT[C/G]ATTAGGATGGGCTCT | 23072 |
rs118028089 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43207806 | TGTCATCTCGTGCAG[A/G]AGCCATGCTTATCTT | 23072 |
rs118048441 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43293414 | GCCCACAATCAGTCT[A/G]ATTGGTTACAAACAG | 23072 |
rs118051924 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43498201 | CCAAAACTCTCAGAA[A/T]ATCGGGCTTAGCATT | 23072 |
rs118056287 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43455149 | TTTGTTTTCTTTTGT[A/T]TTTAATTTGGGAAGC | 23072 |
rs118088005 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43494979 | TTCCCTATTAAGGAC[A/C]TCTCATCCCGTTTTA | 23072 |
rs118124025 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119440 | CTGAGTTTTTATCCC[A/G]ATTGATCTCAACTGA | 23072 |
rs118127714 | snp | A/T | 0.178144 | 0.239451 | intron-variant | HECW1 | GRCh38.p7 | 7:43372540 | CTGTTTTCCTTTTTT[A/T]AGACTTGTTTATGTT | 23072 |
rs118139327 | snp | A/C | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43307414 | CCGTTGATTTCCCAT[A/C]CATACAGAGATTGGG | 23072 |
rs118144171 | snp | C/T | 0.10237 | 0.201756 | intron-variant | HECW1 | GRCh38.p7 | 7:43203018 | TTTTTGGACTCAGCC[C/T]GCCTGCCCCCAGGTG | 23072 |
rs118147612 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43551018 | ATGTTGTGCCACGTA[A/T]TCTATGCTGAGTGGT | 23072 |
rs118150915 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518508 | CTCAAAAAAAAAAAA[C/T]GTATTTGAATATATA | 23072 |
rs118154212 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143911 | AGGAGTATAACTCAT[A/C]ACCTTCCTGGTCAAG | 23072 |
rs118157450 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43406409 | ATAATTTTATTAAGG[A/G]GATAACCTTGGATCA | 23072 |
rs118158858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43412260 | CACTCGTGATCTTTC[C/T]TGTTATAGTTATTAT | 23072 |
rs118178582 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43169960 | AGGGTAAGTGATTAC[G/T]TTGTCTGCCAACATC | 23072 |
rs137855454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43546370 | GCTTGATGACTTTCA[C/T]GGCTTATTCTATAAC | 23072 |
rs137863534 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43495393 | TTATGTTAGTTTGCT[A/G]AGAATGATGGTTTCC | 23072 |
rs137882128 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43347148 | GTGTTTCCATTTGTT[G/T]GTGTCATCTGTGATT | 23072 |
rs137891702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143808 | TTATTTGATGGCCAC[C/T]TGGGGTGGGCACAAG | 23072 |
rs137903211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43539569 | AGCTGAAAATAGTAA[A/T]CTCATTTAATGTTAT | 23072 |
rs137906196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43174207 | AAATATCCCTGCTAC[A/G]TAAGAAATGGGTTTG | 23072 |
rs137917515 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43243498 | CTTCAGGAGTGGATC[A/G]TATGTGAGGATGCTT | 23072 |
rs137944023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43381241 | TATATTCTGGATATA[G/T]TTCTTTGTTATATAT | 23072 |
rs137958269 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43283640 | TTGTTGGTCAGTCCT[A/G]AAACCAAAACGTTTA | 23072 |
rs137960949 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43181253 | TCATGTCTTGATGGA[C/T]ACTTAGGTTGTTTCC | 23072 |
rs137963474 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43209652 | ACAACTGGGTAAGAT[C/T]TGATGGAGACGTACA | 23072 |
rs137980853 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43315112 | CTCTCAAAGCAAATA[A/G]GACTGTTCTGACATA | 23072 |
rs137981108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358596 | TTCAAAAAAATTTAA[A/G]TAGCTGATTAAAATT | 23072 |
rs137985739 | in-del | -/A | 0.030665 | 0.119967 | intron-variant | HECW1 | GRCh38.p7 | 7:43472233 | AGTGGAGGAGACAGT[-/A]AAAAAAAAAGAAATG | 23072 |
rs137991443 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43506204 | GAGCCTTTGTGTACA[A/G]GTATGTTTATTTGAG | 23072 |
rs137993484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43428746 | TTCTGTGTTCTGGGC[A/G]CTCTAAAGTAGGCAC | 23072 |
rs138002851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43330118 | TTGAGAGGCGGGGTC[C/T]ATGTCGCCTCCCCTT | 23072 |
rs138013771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124524 | ACGTTGTGAGCACAC[A/T]TCTCCCAGGACCACA | 23072 |
rs138027323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43265425 | CTAAAGAAGAGCACA[A/G]ATTTTATTACAGAAG | 23072 |
rs138029976 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43191664 | TTGCTTACTCATTCT[C/T]GGGACTTAACACAGA | 23072 |
rs138038510 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43238498 | CTCTAGGGACAAACT[G/T]GATCTTTGGACCAGT | 23072 |
rs138047386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43169288 | GTAAAGCCTAGAGCT[A/G]TGTTTCCCAGGGGCT | 23072 |
rs138049357 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43458909 | TTGTGAAAATCAAAT[A/G]TGTTTGTGCAAGGAG | 23072 |
rs138063278 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | HECW1 | GRCh38.p7 | 7:43279639 | TGTCCCCATTTCATT[A/T]GTTCTGAAGCTGATG | 23072 |
rs138073170 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43351571 | GGGGTGAGATTCCCA[A/G]GAGTGACATCTACTT | 23072 |
rs138094846 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43499594 | TTATAATTACACATG[A/T]CTCTAAAATTACCTC | 23072 |
rs138100469 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43496125 | TATGGGATTGTACAA[-/T]TATGATTTTGCAGAG | 23072 |
rs138101571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43309453 | GACAGTGATCACTGG[C/T]GTAATTTGACAGTTT | 23072 |
rs138116227 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514734 | AATTTAATAATTAAG[C/T]TAAATAATGAAGGAT | 23072 |
rs138119333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120394 | ATACCACTTAGCACC[A/G]CGCAATTTGTTACAT | 23072 |
rs138132678 | snp | A/T | 0.0139214 | 0.082261 | intron-variant | HECW1 | GRCh38.p7 | 7:43424636 | TCAAAAATAAATAAA[A/T]AAATAAATAAATAAA | 23072 |
rs138134592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43340065 | TTACCAGAAACCTCT[C/T]ATCTAGAAGTTTTAG | 23072 |
rs138144362 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43406009 | TCTTGCGCATGCCTC[A/C]TCTTCCTACTTTATC | 23072 |
rs138149251 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43232265 | CCAGAACCCGTCCTC[C/T]ACTGGTGAACTATAA | 23072 |
rs138158094 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43533967 | TCAAGAAGAAGAGAC[A/T]AAGAAGGTCACCCAA | 23072 |
rs138169674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43452798 | TAAAACAAGTGGTGA[A/G]AATAGGCTTCATTGA | 23072 |
rs138172419 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563707 | AACCCCATCTCTACT[A/G]AAAATACAAAAATTA | 23072 |
rs138177590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43528191 | AGCATCCATGATATC[A/G]CAAAACAAAATATTT | 23072 |
rs138177990 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43485845 | TATAAACACTGCACA[C/G]TTAGGCTACACTAAA | 23072 |
rs138184181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133830 | CAGTTTTCATGAGTG[C/T]CTTTTACTTTTCTTT | 23072 |
rs138190088 | in-del | -/GTGTGT/GTGTGTGTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43262247 | TATATGTATGTGTGC[-/GTGTGT/GTGTGTGTGT]GTGTGTGTGTGTGTG | 23072 |
rs138190886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529429 | CTATAGCTCTAGCCC[C/T]GGAGAAAATGAAATA | 23072 |
rs138191153 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | HECW1 | GRCh38.p7 | 7:43203019 | TTTTGGACTCAGCCC[A/G]CCTGCCCCCAGGTGA | 23072 |
rs138204960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43437418 | CTTTTGCACATTTGC[A/G]CAAATTAATCCAGAA | 23072 |
rs138210592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43363007 | AATTCAAATTCTTAC[C/T]TGAAGCACTTTTTCT | 23072 |
rs138233675 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43223990 | CCATCCCCTCTTCCC[A/G]CTCCCACATTCATGT | 23072 |
rs138237313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43164470 | CCAGGGTGTCCTCTG[G/T]ATCGAGCCTTGAGTG | 23072 |
rs138240499 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247278 | ATTTCCTTCTGTTTA[A/G]GGCATGTGCTAGATG | 23072 |
rs138240605 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43200301 | ATTGAAATATTGTCC[A/G]TTAGTACACCTTTGT | 23072 |
rs138258624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43560364 | CTGCCAATCTGTATT[C/T]GTATGTTTCTTCCCA | 23072 |
rs138271225 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43398844 | GGGGCCAGTTAGTCA[A/G]GAGTGCTGATTGGTT | 23072 |
rs138302577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160361 | TGCTTCACTTGTGTT[A/G]TTGTGGTTTAGTCTT | 23072 |
rs138335064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43472345 | CTAGGCCATGTGCTC[C/T]CCCATGTCACTTACA | 23072 |
rs138339899 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43390411 | CCAGGCATGGTGGTG[A/C]ACATCTGTAGTCCCA | 23072 |
rs138349549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43293092 | GGGCGTGGTGGAAGG[C/T]GCCTGTGGTCCCATC | 23072 |
rs138350344 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43190398 | GTTACAGGCGTGAGC[C/T]CCTGCGCCTGGCCAG | 23072 |
rs138362293 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43371982 | CCACCACCACGCCCC[A/C/G]CTAATTTTTTTGTAT | 23072 |
rs138369339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43270479 | AGGGAGCCAGGAGAC[C/T]GAGGTAGAAGCTGCA | 23072 |
rs138377876 | in-del | -/GAAA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247974 | AAGAAAAAGAGAAAG[-/GAAA]GAAGGAAGGAAGAAG | 23072 |
rs138393344 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135361 | AGATCTGGAATGTTA[C/T]TGTAATGGCTAGAGT | 23072 |
rs138398397 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43369239 | CGAGGCAGGCAGATC[A/T]CCTGAGGTCAAGAGT | 23072 |
rs138401202 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43334342 | AACAACCAGGAAAGT[G/T]TTCAGAGTCCAAACA | 23072 |
rs138408950 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | HECW1 | GRCh38.p7 | 7:43425246 | ACACACACACACACA[C/G]ACGTGTACATATATG | 23072 |
rs138423611 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43349657 | TAAAGTTTGTTTTGT[C/G]TTATATAATAATAGC | 23072 |
rs138425601 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43249664 | CTTCAGGCAGCATGT[A/G]GCCAAAAAACATGCG | 23072 |
rs138428244 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299089 | CCTTGAATCTATTAC[C/T]GTATCCTCGAGGCCA | 23072 |
rs138429003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43257130 | GCTGTGGGGCCACCC[A/G]AATGCACAAGACACA | 23072 |
rs138430598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150687 | TCAGGCCTGGATCAG[C/T]ATTTTAAAGATGGCG | 23072 |
rs138433785 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43547284 | CCAGGCATGGTGGCT[C/T]ATGCCTGTAATCCCA | 23072 |
rs138433807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43178737 | CAGCTAGAGGTTGGG[C/T]AGCAAGGGGGACTGT | 23072 |
rs138442355 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116673 | AACAGGACAAGCTAC[A/C]TTAGGAAACCAGGAA | 23072 |
rs138446419 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511145 | GATGAGGGCTTGACA[A/G]TGCCTGTCCTCGAAA | 23072 |
rs138454177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43254242 | CCCAGGAGACCAAAC[A/C]CAGAAGATCTTTTTT | 23072 |
rs138471133 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43433492 | GCTAAGACCCACTGG[A/T]CAAAGCAAAAGTAAG | 23072 |
rs138471994 | in-del | -/G/GA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43165404 | CTTTTGGCGGGGGGG[-/G/GA]GGTGTTTGTGTGTGT | 23072 |
rs138483563 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43365251 | AGTCTTTCAAGTCCC[A/G]AGCATACTGCTCCCA | 23072 |
rs138489968 | snp | A/C | 0.0265845 | 0.112187 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43466514 | GCTGCTGCAGTCCCC[A/C]GCGGTCAAGTTCATC | 23072 |
rs138505794 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43459153 | CGTGCCCCAGGAAGC[C/T]GTCCCAGAATCCCTC | 23072 |
rs138506769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43504457 | GCAGCGTAGATTCTG[C/T]GGTTCATCATTTCAA | 23072 |
rs138525958 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377481 | AGATCCCACTTCTTT[A/C]AACCATCTAAACTAG | 23072 |
rs138528518 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156062 | TTAAGAACACTTAAC[C/T]GGGGGAAATAAATTC | 23072 |
rs138532111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43552752 | ATGTTTCAGTATTTT[A/G]TTCCTTTTTATAGCC | 23072 |
rs138532286 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43222060 | CTGCAGGCCATTCAT[A/G/T]TGGACGTTAAGGTTT | 23072 |
rs138534346 | in-del | -/GTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43325963 | AGTCCGTTGAGGCTG[-/GTT]TTATAACAAAATACC | 23072 |
rs138550885 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43500214 | AAGCGATTCTCCTAC[C/T]TCAGCATCCTGAATA | 23072 |
rs138555977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286990 | TAATTTGCTGTGTCC[C/G]GGGCATTGTTTAATG | 23072 |
rs138567715 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43264716 | AGGTGTGGTGGCGGG[A/C]ACCTGTAGTCTCAGT | 23072 |
rs138572343 | in-del | -/TTATTATTG | 0.304688 | 0.243945 | intron-variant | HECW1 | GRCh38.p7 | 7:43315457 | ATATCTCCCGTCCCA[-/TTATTATTG]TTATTATTATTATTA | 23072 |
rs138583288 | in-del | -/ATGG | 0.48251 | 0.0918641 | intron-variant | HECW1 | GRCh38.p7 | 7:43530505 | TTTTCCATATCTTTT[-/ATGG]ATGGATGGATGGATG | 23072 |
rs138583960 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152284 | GAAAGATAGTACATA[C/T]GTGAGACAGTTATAA | 23072 |
rs138587768 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43372396 | TAAGTTCTAGGGTAC[A/G]TGTGCACAACGTGCA | 23072 |
rs138588837 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43450696 | GAATGTAGCAAACTG[-/AC]ACACACACACAAATG | 23072 |
rs138589174 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43199944 | AATTCTGTTTGTATT[C/T]AGGGGCATGGTTATA | 23072 |
rs138598285 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128573 | ATATACAAGGAGGTG[A/G]ATGTTGTTTTCATGC | 23072 |
rs138618984 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43318678 | GGCCCTTTGGCTTCA[A/G]GCTCAGTGCTTTTTG | 23072 |
rs138626173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43243199 | TACCTGGATTAAGAG[A/G]GCCCTGACAGATGAT | 23072 |
rs138648701 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43560655 | CTGCATCAGCCTGGG[A/C]AGTGATCTGATACTC | 23072 |
rs138651978 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43349079 | TGCTCTGGTTGCCCA[G/T]GCTGGAATGCAATGG | 23072 |
rs138656256 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43538293 | CACTCATGTCCCTGG[A/C]GTTCCTGAGGCCCAA | 23072 |
rs138667568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43204546 | AGACAGGCATGGCCA[C/T]GCCCTCATGGAACTT | 23072 |
rs138681655 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159931 | TGATCTGCCCGCCTC[A/G]GCCTCTCAAAGTGCT | 23072 |
rs138682289 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43228553 | GAGAAGAACACTTGC[A/G]TGGATCACCAGCTGG | 23072 |
rs138691496 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43556066 | ATCTAGGGAGAACAC[A/G]GCCTGATAGTAACTA | 23072 |
rs138695624 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152212 | TTCTGGGAAAAAAAA[G/T]GTTCAAGGACCTATA | 23072 |
rs138699890 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43368821 | CATCCTTCCTGTCTG[A/G]ACTCTAAGAAGCAAA | 23072 |
rs138702460 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43388297 | TGGTTATTATGCAAT[A/G]CAATAATGGCCAACA | 23072 |
rs138705455 | in-del | -/ATGCCTGACA | 0.162581 | 0.234218 | intron-variant | HECW1 | GRCh38.p7 | 7:43397854 | TTAGCTTGGGCTCAG[-/ATGCCTGACA]ACATCATATGTTAAT | 23072 |
rs138708328 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43277404 | TTGTTTTAGGTGTTT[A/C]GCAGCCTGAAGCCAT | 23072 |
rs138712041 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43447587 | AGGCCATGCACACGC[C/T]GGCATGTGACTTCTT | 23072 |
rs138724641 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43384651 | AATCATTTTCTAGGC[A/G]TCTTTTCATTCAGTG | 23072 |
rs138729162 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43436520 | TTGGGTAGACAGTGG[A/G]AAATTATAGTCAAAG | 23072 |
rs138735204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43320078 | TCTGGCAGATGGTTA[A/G]ATTTCAGCTGCTGAA | 23072 |
rs138769922 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43461244 | ATATTAGGAGGTTGA[C/T]GCTGGCTGTGGGCTG | 23072 |
rs138777725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43528477 | CACAAGCTAACCAGA[A/G]TGATGGGTCAAAAAA | 23072 |
rs138805175 | in-del | -/AA | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43294123 | CGCTGCTGCAGGGGC[-/AA]ACTCTCATGTGCATT | 23072 |
rs138809008 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43394068 | CTTTAGCCATTGATT[A/G]TTAATTGTCCTGGTG | 23072 |
rs138820151 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124147 | AACGATGTAATCGAC[A/G]CACTATTTTTATAGA | 23072 |
rs138820458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43453513 | TGAGATGTCATCCAG[C/G]TAGTAATGTCAAGAA | 23072 |
rs138835049 | in-del | -/AGAG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248008 | GAAGGAAGGAAAGAA[-/AGAG]AGAAAGAAGAAAGCA | 23072 |
rs138838335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520021 | AAATTACATCTGTGG[A/G]TAAAAAATAAATAAA | 23072 |
rs138853851 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43168279 | GAGAGACAGAGAGAG[A/T]GAGACAAGGAAACAT | 23072 |
rs138853859 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121557 | CATATAGTGATATGT[A/G]AAATCACTATATTAT | 23072 |
rs138860554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43551175 | GGAGAAGTGCACTGG[C/T]CATGGTCTTGTCCAC | 23072 |
rs138866714 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43524792 | CTCTAGCTCTCCCGT[A/G]TGCTTGTAATATTTG | 23072 |
rs138873309 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43431883 | CACCGACACTTGCTT[G/T]TTTTTTTTTTTGAGA | 23072 |
rs138902004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43164840 | TGCAGCCGCGCTTCC[A/G]TGGTGTATGATTCAG | 23072 |
rs138908700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43173725 | TCCCGCTGTGCAGCC[C/T]AGTTCCAAACAGGCC | 23072 |
rs138914026 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43232973 | ATTACTGTGTTTAGT[G/T]GTAGAGACCCAGTTT | 23072 |
rs138929173 | in-del | -/C | 0.0437281 | 0.141251 | intron-variant | HECW1 | GRCh38.p7 | 7:43175027 | GAACAGCTCGAGGTA[-/C]CTATGGGCTCCCCAA | 23072 |
rs138934151 | in-del | -/TTC | 0.0663309 | 0.169604 | intron-variant | HECW1 | GRCh38.p7 | 7:43393669 | AAAACATACTCTTTT[-/TTC]TTCTTCTTTTTTTTT | 23072 |
rs138935801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146770 | GAAGATGTGCCAGGC[A/T]AATCAGGAGCCAGTG | 23072 |
rs138948093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43365110 | TCCCACTCTCAGGCA[C/T]CCAGCCGGCATCATC | 23072 |
rs138954207 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43292987 | CCCATCACTTTGGGA[A/G]GCCAAGGCGGGTGGA | 23072 |
rs138956130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43250597 | AGCGCCAGGAACGTC[C/T]TGTGTGTACCTGCCC | 23072 |
rs138956980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43433759 | CTTTCTTTTCTGACC[C/T]GAGTGCCAGTAGACT | 23072 |
rs138965696 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43178833 | GACCTTCAAGGCTTA[C/T]AAAGATCCTTTCATT | 23072 |
rs138965700 | in-del | -/CCCT | 0.490175 | 0.0693959 | intron-variant | HECW1 | GRCh38.p7 | 7:43353629 | CCATATCCACAATGC[-/CCCT]CCCTCCCCTCAATCT | 23072 |
rs138972097 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43334629 | GCTGTGTTACCTGAG[G/T]AAAGTAAGCAGACAA | 23072 |
rs138974460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43208315 | TTGCTTCTTTTGCAA[A/G]TCAACTTGGTCTTTT | 23072 |
rs138979625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43257965 | GCTCATTAGTCTTCC[C/T]AATCCTATGAATCTG | 23072 |
rs138980317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283464 | GGAAAATGTATTTAT[G/T]TTGCATAAAATATGT | 23072 |
rs138989886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43288529 | TAGAAGATGAGATGT[C/T]ACAAGGCAGAGCTTT | 23072 |
rs138995492 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43450161 | CTCTTGTCCTTTCCT[C/T]TTTCCGGAGCACCCT | 23072 |
rs138998404 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43362743 | GAAGGCACTGAGCAC[A/C]CAACAGGCAGAGAAG | 23072 |
rs139001946 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43558961 | AGAACAAGGCTGTAG[A/T]TAGGCAGTGGAAGAA | 23072 |
rs139017300 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43271704 | TAAATCATGGATGAC[A/G]GAATCAAATAGAAAA | 23072 |
rs139018232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298610 | GTGTGTGAGGCATTA[A/G]GACTCAGTAGCATGT | 23072 |
rs139018918 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43400458 | GGTAAACAACAGAAA[G/T]TTTGACTTGAACAAT | 23072 |
rs139024296 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43370317 | GTACCAAAGATACCT[A/G]TTAAAATAGCCAAAA | 23072 |
rs139027899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43481611 | GATTGAATAGCCCAA[A/G]TAGAGTTAATTTAAT | 23072 |
rs139045122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43223071 | TCCTCATCTTAGTTC[A/G]TGGCCAATCTATTCT | 23072 |
rs139055063 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43382292 | CTCCGTCTCAAAAAA[A/G]AAAAAAAAAAAAAAT | 23072 |
rs139065292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43491662 | GGCCAGAGTGATTTC[A/G]GCTCACAGCAACCCC | 23072 |
rs139086638 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43225306 | TGAACTGCACAGATG[G/T]TGGGAGAATCAACTC | 23072 |
rs139094707 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300662 | TATATCAGATATGGC[C/T]GTGTTCATCCGGGGC | 23072 |
rs139106170 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412446 | TTATTTATTTATTTA[C/T]TTATTTATTTATTTT | 23072 |
rs139110240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43343156 | ACTCTGGTTCATAAG[A/T]TCTCAGTGTTTTTGC | 23072 |
rs139113591 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43293310 | AGCAGCGGTTCAAGG[A/G]CCCGAATACAGAATC | 23072 |
rs139128147 | in-del | -/A | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43317128 | TAGTGGTCTTAGACC[-/A]AGGCTCTTGGGCCTG | 23072 |
rs139130427 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43345458 | ATTTTCCATAAGTTA[C/T]TGGGGTACAAGTGGT | 23072 |
rs139138149 | in-del | -/TCTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336015 | CTTCCTTTCTCTTTC[-/TCTT]TCTTTCTTTTTCTTT | 23072 |
rs139143868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43407337 | TGCAGAGGAATTTTA[C/T]ACCCGGACCCATCAA | 23072 |
rs139145913 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43458074 | TAGACATGAATGGAC[C/T]AAAAATCCATGGGAG | 23072 |
rs139152317 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43340557 | CAAGCAATAGCCCCA[G/T]GGATCAAAAACTCTG | 23072 |
rs139174136 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43216309 | CACCACCATGCCCAG[C/G]TAAGTTTTGTATTTT | 23072 |
rs139177024 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355037 | CTGAAAGGAAAAAAA[-/A]AAAAAACTGCCTCCC | 23072 |
rs139188479 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43512856 | CACTCAGGATTGACA[C/T]GGTACTCAGCTGTGG | 23072 |
rs139190363 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118837 | TGCATATAAAGAGGA[A/T]GATGATAAGGAAATA | 23072 |
rs139200527 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43336867 | CCATCCACGTTGCTG[C/T]GAAGGACATGATTTT | 23072 |
rs139202271 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43471568 | GCTCTGCTGCTTCAG[A/G]AGGACCGGGGCAAAG | 23072 |
rs139205834 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | HECW1 | GRCh38.p7 | 7:43259223 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAACAT | 23072 |
rs139224459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161550 | CCAGTAGTGCATGGT[A/G]CAGTGAGACACATTT | 23072 |
rs139225242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43341890 | TTTAATGATAATTTT[A/G]CTACAAAAATATCAT | 23072 |
rs139243800 | in-del | -/T | 0.499767 | 0.0107802 | intron-variant | HECW1 | GRCh38.p7 | 7:43374839 | ATGAAAATATTTTTT[-/T]ATCTAAAAAAATACA | 23072 |
rs139245099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135932 | TCACAAGGCCTTTTA[C/T]GCTTTTATGACATTT | 23072 |
rs139259150 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43175946 | CAGAGCACATTTCCT[C/G]TTAATGCTCACAGTG | 23072 |
rs139267824 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43383106 | TACCTGCAAAGGACA[C/T]GAACTCATTATTTTT | 23072 |
rs139272139 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307888 | CATTTCACTATATAT[-/AT]ATATATATATACACA | 23072 |
rs139274734 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43463507 | GATACTTGTCTTGCT[A/G]ATTGTTCTGGCTATC | 23072 |
rs139280560 | in-del | -/AAG | 0.117188 | 0.211804 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158413 | AAAGGATCAAGTAAT[-/AAG]AACTTACCCATTATC | 23072 |
rs139290339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43285496 | ATCAGGAGTGCAGTC[A/G]GGAATGAGCCCACCC | 23072 |
rs139290871 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43467362 | CAGGCAGAGGGACAT[C/T]TGTAGAAAGGATGCA | 23072 |
rs139292531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43211647 | TGCTAGAATAAACCT[A/G]TGTTCATAATAACCC | 23072 |
rs139293582 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508434 | CTAATTTAAAAAACT[A/C]TTTCTCTTAAAGTGC | 23072 |
rs139305304 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43549428 | TATGTATTTTTTTCT[A/T]TAAACCAGTAACTAA | 23072 |
rs139309178 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43331961 | TCCAGAGAACAGTTA[C/T]GGGACAGGACTTTCC | 23072 |
rs139319341 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43395284 | TTTAAACTGTAAACT[A/C/G]CAAACTAAGTTTCTC | 23072 |
rs139330874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511277 | GTGCATCCTGGAAAC[A/G]CAATTGCAGGTAGCT | 23072 |
rs139332885 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43187459 | TTTGATTCGTGCTTT[C/G]AAATTTTAGGGTTTT | 23072 |
rs139338489 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43417581 | GAAAAAATATGGTTC[C/T]GCCCAGTGAGGTGGC | 23072 |
rs139339162 | in-del | -/T | 0.321042 | 0.266402 | intron-variant | HECW1 | GRCh38.p7 | 7:43455127 | CACCTTTTTGTTTTC[-/T]CTTTTTTTTTGTTTT | 23072 |
rs139345138 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43220573 | CTAGCATAAACTATT[-/A]GAGCCTGCCGTGAAT | 23072 |
rs139347103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117657 | TTTAGGTGTCTTAAA[A/G]CCTCTTTAAATATTT | 23072 |
rs139354461 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43240213 | CATGGTGGTGGGCGC[C/T]TGTAGTCCTAGCTAC | 23072 |
rs139355363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43346078 | TTGCCACACTGTTTT[C/G]CATAGTGGCTGTACT | 23072 |
rs139362763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43535192 | TCAAGTCAACAAACA[A/G]CAATGCGCTGAAGGG | 23072 |
rs139363649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43170637 | GGTTGCATTTGAAAG[A/G]GCCTTGTCAAAGGTG | 23072 |
rs139377219 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43354620 | CGCAGAGGAGAAAAA[A/G]GAAAAAACAATAAAA | 23072 |
rs139377891 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43189189 | ATATAAGGACAGAAA[C/G]AAAGAACAAATCTCT | 23072 |
rs139384411 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43459744 | GGTCTCACCATGTTG[A/G]CCAGGCTTGTCTCGA | 23072 |
rs139395375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43184639 | CTGGGGAGCAGAGAC[A/G]GGCTAAAGGTTGAGT | 23072 |
rs139395768 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43281055 | TTCTAGGATCCTGCA[C/T]TCATTGACTGGGGGA | 23072 |
rs139397460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43228153 | AAAATTAAAAAGCAA[A/G]TAACGCCCAGGGAAA | 23072 |
rs139420403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43306335 | TATACATTTCTTGGT[C/T]TGTAAATTTTCTCAA | 23072 |
rs139421471 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43480533 | AAACAGCTTTTAGAA[C/T]TGGATTATCATAAGG | 23072 |
rs139425230 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43525023 | CCTAATATAAAATAG[A/G]GATTAAAAATTATGC | 23072 |
rs139439384 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43486833 | AGACACAGGTACACA[C/T]AAAAATAAAGACATT | 23072 |
rs139442607 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43229694 | TTCAAGCAAAAACTA[A/G]TTAATGGATGGTAAA | 23072 |
rs139442837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43185319 | GCAATATCCTTTACA[A/G]TAAACTGGTAAACGT | 23072 |
rs139447850 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308614 | TACTACTAAATTATC[A/G]TGCCTTTCTGTAATT | 23072 |
rs139448720 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517315 | CAAGGCCCTTTGCTA[A/C]CTGCAAAATAAACAG | 23072 |
rs139450696 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43309832 | TCAGTGACGGAGCCT[C/G]GCTGAGTGCCCAGGC | 23072 |
rs139465175 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43196839 | ATTTGTAATATTTTA[C/T]ATTCATGTGCATCAG | 23072 |
rs139465317 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521667 | GATCACCTGAAGTCA[A/G]GAGTTCAAGACCAGT | 23072 |
rs139484352 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43529961 | TATTTTTATTTATTT[A/T]TTTTTTGAGACAGAG | 23072 |
rs139510326 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43245461 | TTCAGGAAGAATGCC[A/G/T]CCTCTTTCTTCTTTC | 23072 |
rs139512195 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43321907 | TGGTATCCCCGCTCC[C/T]GGCAATGACACCAAT | 23072 |
rs139529280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43239979 | ATCATATTGTTTGTC[A/G]TCCGTATGGCTTGGC | 23072 |
rs139540688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126036 | AAATCCATGTAAATG[C/T]AAGGCGTGCGTGTAT | 23072 |
rs139543015 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122959 | ATGTGAAAAGCATTT[A/C]GGTTCTTTTGTGTGT | 23072 |
rs139544422 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43482331 | GACTCTGGTATCAAA[A/T]TAGAGGGGAGTGGGT | 23072 |
rs139545924 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43434163 | ATAGATTTTGTCTGC[A/C]TACTAAGCATTTGAA | 23072 |
rs139554208 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359524 | GTTGTTCTGTATAAT[A/G]AGTAATGTTGTTTGA | 23072 |
rs139594118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43235870 | TGGATAAAAATGCAA[A/G]CACAGCTAAGAGAAC | 23072 |
rs139597211 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43556180 | GTTGCCTAGAGAACA[C/T]GCCACTAAAAAACTG | 23072 |
rs139606535 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | HECW1 | GRCh38.p7 | 7:43256381 | TTGGGAGGCCAAGGC[A/G]GATGGATCACCTGAG | 23072 |
rs139624981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295738 | TGTTTATATCCCACT[A/C]TCTCTCAGTCTCATA | 23072 |
rs139633820 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43478372 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 23072 |
rs139633905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43430594 | AGAGCTGTTTAAGCC[A/G]ATTTGTCTATAGCTG | 23072 |
rs139637225 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43356464 | ATGATCATAATAGGG[A/G]ACTTCAATACCCCAC | 23072 |
rs139641588 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43293915 | CGACATTAGATTTTC[A/G]TAGGAGCATGAACCC | 23072 |
rs139642318 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | HECW1 | GRCh38.p7 | 7:43176225 | TTGTGGCTGAACTGT[-/A]AAAGAAACTCTCAAT | 23072 |
rs139642511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43367337 | CTAAAAGGAAACCTC[A/T]TTAACAATACTATGA | 23072 |
rs139642778 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43192610 | ATATTAATAACTTAC[A/G]CGTGCTTATTTTAAG | 23072 |
rs139647688 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157448 | GACTGTAATATTCAG[A/T]TACTTACATGAAAAC | 23072 |
rs139660295 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122664 | CTTGAGAAAAATAGC[A/G]GAAATTCACAAATTG | 23072 |
rs139664765 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43171177 | AAGTAAAATGCTTGA[-/C]TTTCTTATGCGGAAT | 23072 |
rs139679506 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43405114 | AGGATATAATCTCTA[-/C]CCTTGCGGAGTTTGT | 23072 |
rs139684963 | in-del | -/C | 0.186421 | 0.24178 | intron-variant | HECW1 | GRCh38.p7 | 7:43556696 | TGTCTCAAATTAAAT[-/C]TAAAAAAAAAAAAGA | 23072 |
rs139686720 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43206409 | GTGCTTTTTTCTGGT[C/T]TTTTATTTTTTGTCT | 23072 |
rs139693821 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43407935 | ACAGTACTAACACAC[G/T]TTTCATTGCACTGCA | 23072 |
rs139696422 | snp | C/T | 0.040671 | 0.13668 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137774 | AGGCTGGTCTCGAAC[C/T]CCTGAGCTCAAGTGA | 23072 |
rs139705334 | in-del | -/TAC | 0.186421 | 0.24178 | intron-variant | HECW1 | GRCh38.p7 | 7:43551429 | AGAAGGGATGGAAAA[-/TAC]TACAGTCGTTTTAAT | 23072 |
rs139714300 | in-del | -/GGAA | 0.493477 | 0.0567349 | intron-variant | HECW1 | GRCh38.p7 | 7:43466023 | GAGGGAGGGACAGAG[-/GGAA]GGAAGGAAGGAAGGA | 23072 |
rs139718142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140558 | TCATTTATCTTCTTT[C/T]GTTACTTTTTGAAGG | 23072 |
rs139724707 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43426872 | TTCTATTTATTTTCA[A/C/G]AATGTTTTCATAGTA | 23072 |
rs139729816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43290706 | CATAACGTCCAGAGC[C/T]CCAGTGACAAGTAGT | 23072 |
rs139737337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43327287 | TGCAAGATAATAGGC[A/G]TATTTATATTATTGT | 23072 |
rs139742576 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43205316 | TCTCAAACTCCTGAC[A/G]TCATGATCGGCCCGC | 23072 |
rs139747580 | snp | A/G | 0.0079613 | 0.0626594 | intron-variant | HECW1 | GRCh38.p7 | 7:43251912 | AGAAATTCAGCAATC[A/G]CAAGAGGCAGTGTCA | 23072 |
rs139748230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43483694 | GTTGGGATTACAGGC[A/G]TGCACCACCACACCT | 23072 |
rs139750270 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136710 | CACAGTTTTGCAATC[C/T]AACCCATCCAAACTG | 23072 |
rs139755500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43532040 | CTCCACAGCTCCACT[C/T]AGATATAAATAGGCA | 23072 |
rs139757102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43548836 | ATAGTCCCAGTTACT[C/T]GGGAGGCTGAGGTGG | 23072 |
rs139758946 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43469174 | GAAGCTAGCAAGGGC[A/G]TGAGGAGGAGAGTGT | 23072 |
rs139762790 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43326699 | GAAATGAACATATTG[C/G]TGTCTTGGTGACAAT | 23072 |
rs139763375 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152768 | GAGCTCACTTCATTC[C/T]GGGGGCCCTCGGGTC | 23072 |
rs139763552 | in-del | -/CCTCCT | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248671 | GGCTGCTTTACTCTC[-/CCTCCT]CCTCCTCCTCCTCCT | 23072 |
rs139776994 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43202160 | ACAGAGGTTGAGTAA[A/C]TTGCTGAAGGATACC | 23072 |
rs139789335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43403229 | ATAGGAGATACCCAG[A/G]GAAAATGAGTAAATC | 23072 |
rs139790361 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43438651 | GATTCTCATGGAATG[A/G]CAGCAATTAAGATGC | 23072 |
rs139801251 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43263521 | GTGTGCCACTATGGC[C/T]GGCTAATTTTTATAT | 23072 |
rs139826228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43188864 | CCTGCCATCTTGTCA[C/T]TGGGGTTAGAAACAA | 23072 |
rs139830449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43373955 | GTTCAACCATGTTGC[C/T]GCGTGTGCCAGAATT | 23072 |
rs139837005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43454666 | GACAATCCATCAGGT[C/G]AAGCATAAGCCATCA | 23072 |
rs139840356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43375210 | GGAGAAACTGTCGGA[C/T]GCCTGGAAAATAGCA | 23072 |
rs139844243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43548158 | AATTTTAACTTTTTA[A/G]TAATAGATTTGTGTA | 23072 |
rs139856460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43450991 | TCTAAGCAGGTCAGT[A/G]TGAATTTGTGTGTAA | 23072 |
rs139859953 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43277694 | TTTACCACACATTGT[C/T]TTCTCCCCTCTTCCA | 23072 |
rs139873287 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147982 | CAATTTGCAAAGCTC[A/T]TCCCCCAAAGGCATA | 23072 |
rs139879119 | in-del | -/T/TT | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43338822 | GGGATCATTTTCCTC[-/T/TT]TAAAAAAAAAAAAAG | 23072 |
rs139883170 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43542781 | TAAGGGATCTCATTC[A/G]TTCAAACCAATTCCT | 23072 |
rs139893715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43435850 | ATATTTAATCTCTGT[A/G]AATAGAAATCAACTA | 23072 |
rs139893971 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43201553 | GAACAGCCAGTGTTC[A/G]TTCATCTTTACATTC | 23072 |
rs139902958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512312 | CTTAATGGACACCCA[C/T]GCCCTGCCCACCTCC | 23072 |
rs139919414 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160714 | ATTAATTTTCTTTTT[C/T]TCAAAATTTCTTTAG | 23072 |
rs139919755 | snp | C/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112885 | GTGCGCCCCCCAGCT[C/G]TAATCTGCGCGCTGA | 23072 |
rs139923759 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43557035 | GAAAATAACTCCCTG[A/T]ATAGTGACCCCTGTC | 23072 |
rs139923963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43496979 | ATGAATTTACAATCT[A/G]CTGAGGGAGACAGAT | 23072 |
rs139925303 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43258711 | GGCACTAACTGAAAA[C/T]GTACTTGTTAAATTG | 23072 |
rs139930530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421296 | GTCTATTCCAAATCA[A/G]TTGTACATTTAGATA | 23072 |
rs139937610 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141729 | TCTTGAACTCCCGAC[A/G]TCAGGTGATCCGCCA | 23072 |
rs139939538 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43184837 | GCCTCAGAAAACTTA[C/G]AGTGATAGCGGAAGG | 23072 |
rs139952627 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43321159 | AAGGCTTCCTGCCCA[G/T]GGTCCCAGTCTGTCA | 23072 |
rs139953396 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158294 | ACACACCAGTTTTCC[A/G]ATTTTCTTTGAGATT | 23072 |
rs139957234 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43224821 | CAAATGAAAACCAAA[C/G]AAAGAAAGAAAAAGG | 23072 |
rs139970379 | snp | A/G | 5.69914e-05 | 0.00533783 | missense | HECW1 | GRCh38.p7 | 7:43554619 | GGCATCTTGTGATCC[A/G]CTGGTTCTGGGCTGC | 23072 |
rs139975817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43344236 | TGATGGTAGTTTCTT[C/T]TGCTGTGCAGAATCT | 23072 |
rs139986042 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153866 | ACTATTTTATTAGAA[A/C]AAGGCACTTCTAGGT | 23072 |
rs139989356 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43220371 | TGAGTCTTCACGTCC[A/G]GAGTTGTTATTGGAG | 23072 |
rs139993116 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43266429 | CGTCCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 23072 |
rs139994965 | in-del | -/A | 0.281841 | 0.247964 | intron-variant | HECW1 | GRCh38.p7 | 7:43356830 | TTTTAAAATTTTTTG[-/A]AACAAATCAAATAGA | 23072 |
rs140008624 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43182529 | TGTCTGTTTTTATGC[C/T]AGTACCATGCTGTCT | 23072 |
rs140012029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43281961 | TGACACTCTCTCCAT[A/G]AGCCTTTTTCGAGTC | 23072 |
rs140013449 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43284525 | AAAAAAAAAAAAAAA[-/G]ACAGAAACAGAAGGA | 23072 |
rs140021181 | in-del | -/TT | 0.311999 | 0.24219 | intron-variant | HECW1 | GRCh38.p7 | 7:43347268 | TTTAATTTAATTTAA[-/TT]TTTTTTTTTGCAGCT | 23072 |
rs140057491 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43267668 | ATCTAAAAATATTTA[C/T]TTGGGGGACCAAACA | 23072 |
rs140069066 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515801 | TTGTGTCATTGGAAA[C/T]TCTTCACTTACTTGC | 23072 |
rs140078788 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | HECW1 | GRCh38.p7 | 7:43322129 | GGCTGGAGTGCAATG[A/G]CACAATCTCGGCTCA | 23072 |
rs140085751 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43387254 | TTTGAATGGATCGAG[A/G]TTATGGAAACGGATT | 23072 |
rs140091997 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43208463 | GGGGTTAAAGTCTCC[C/T]GGTCTTTCACCTGCT | 23072 |
rs140097642 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118458 | AATAAAATTAAACAT[A/G]TAAGACCTTGCCATC | 23072 |
rs140104497 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43455019 | GCTCTTCTATGTTTC[A/G]CTCAGACGTGAACAC | 23072 |
rs140110354 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43429492 | TTCTTAATGTAAAAC[A/G]CTGTTACATTGCTAG | 23072 |
rs140114519 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43378450 | AGCTCTCTCAGATAA[A/C]CTGCCTTAGAAAGAT | 23072 |
rs140116704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43530812 | TACCTCCAAATTGTT[C/T]GGCATGATGCCCTTG | 23072 |
rs140123249 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43329947 | TGCCATGTTATTCTG[A/C]TATGCCTGTAAATGT | 23072 |
rs140132317 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130145 | CACTCAAAAACACCT[A/G]TGTTCATTTAGCAAT | 23072 |
rs140149282 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140409 | TCTTGTCAGTTCTCC[-/A]AAAAAAATCCTACTG | 23072 |
rs140152916 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43311295 | GGGACCACTCCTAAT[G/T]CTGGGCTGTGTGTAG | 23072 |
rs140158082 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43253351 | AGTGATGATGACGGT[A/G]ATGACCATGGTGGTG | 23072 |
rs140162823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154676 | AGGAAATTTCAAGAA[A/G]GCCCTGTATTCCAGC | 23072 |
rs140165161 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43175482 | TTGTCATTATTTTTA[A/G]AGTTAAACTTTCTCT | 23072 |
rs140174747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43501532 | TACAGTTTGAAATGG[C/T]TGGGAAAAAAATGTT | 23072 |
rs140180839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43440636 | TAAATGCAAAGCATA[A/G]TAAATGTAATTTTTG | 23072 |
rs140186624 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43550326 | ACTCCAGGGATAATA[A/G]TGCTGAATAATGCCC | 23072 |
rs140197154 | in-del | -/T | 0.105214 | 0.203807 | intron-variant | HECW1 | GRCh38.p7 | 7:43180405 | ATTTTTATTTTTTTT[-/T]GAGATGGAGTCTTGC | 23072 |
rs140200792 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43284615 | TATTATCTACAGTTA[A/C]CCTGTTGTACAATAG | 23072 |
rs140205352 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43264391 | CCTGAACATCCTCCA[C/T]GTTCATCCAGGTTAT | 23072 |
rs140216828 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43364797 | AGTAGCACCTATCAC[A/G]TTTTATGTCTTTCTT | 23072 |
rs140227336 | in-del | -/A | 0.115088 | 0.210473 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125600 | CTGTACTAAAAATAC[-/A]AAAAAAAATTAGCCG | 23072 |
rs140230201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43183261 | TGAGAACAGCTCTTC[C/T]ACTTCTACCACAAGT | 23072 |
rs140230656 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190094 | GGAAATTTTTGTTGT[C/T]GTTGTTGTTGTTTGT | 23072 |
rs140235511 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43504739 | CATTTCCCCTAAAGC[C/T]TCCAACCCTCAGCAC | 23072 |
rs140247221 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376608 | AGTGGCTTACACCTA[G/T]AATCCCAGCACTTTG | 23072 |
rs140250479 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43440018 | GCTCCTCCTCCAAAG[C/T]CTTCTGCTTCCACAG | 23072 |
rs140254421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297251 | AATTAGATACAGTCA[A/G]AGCAAGGGCACATTT | 23072 |
rs140263619 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43180774 | CTCAGTACATGTGCA[C/T]ATTGTTTAATGAACA | 23072 |
rs140289643 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43292046 | TGGGGCTGAGAGAGA[G/T]AAACTCTTACAAATG | 23072 |
rs140290258 | snp | A/C | 0.499609 | 0.0139722 | intron-variant | HECW1 | GRCh38.p7 | 7:43344064 | TGTCTTCTTTTGAGA[A/C]GTGTCTGTTCATATC | 23072 |
rs140293389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43202577 | CTCCCGGGTTCAAGC[A/G]ATTATCGTGCCTCAG | 23072 |
rs140297442 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43499145 | AATTAGCCAAGCCTG[A/G]TGGTGTGCGTTTGTA | 23072 |
rs140297561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43217760 | GCTCTTGGCGTATGG[C/T]TTGGAGGACTTCAAA | 23072 |
rs140304141 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43166122 | AGAGTTTCACTCTTT[C/T]GCCCAGGCTGGAGTG | 23072 |
rs140310383 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43561565 | TATAATCAGTTTGCT[A/G]GTGTCATTCTAGTGT | 23072 |
rs140317574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43427415 | CAGAGCTCTTTTTCT[C/T]AGAATTGTCAACATC | 23072 |
rs140320902 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351501 | GGGGGCAGGGCTAGA[A/C/T]GTGTCTGAGCTCAGA | 23072 |
rs140331807 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152211 | TTTCTGGGAAAAAAA[A/T]TGTTCAAGGACCTAT | 23072 |
rs140333680 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521375 | TAGGAGGCAAAATCA[-/CT]CTGTTGAGAATCACT | 23072 |
rs140348052 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43387502 | ACTAGAGAAACAGGA[C/T]CATCCATCTTCAGGT | 23072 |
rs140363043 | in-del | -/GTG | 0.0322114 | 0.122752 | intron-variant | HECW1 | GRCh38.p7 | 7:43171235 | TTCCATATATTCTGA[-/GTG]GTGGGAAATGTGATT | 23072 |
rs140364319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43470484 | AGGCTTCCCAATGCA[A/G]TAAGCCCTAGTTCTC | 23072 |
rs140364371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43424332 | GTTACTAAAAAAATA[C/T]GAACAGGCCAGGTGC | 23072 |
rs140364881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43200464 | CTCTTCAGCAAACCC[A/G]GCAGCCAAGTCAGAT | 23072 |
rs140366925 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162533 | AATAATCCAGGATGA[A/G]CTTTTATCTCAAGAT | 23072 |
rs140367562 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149737 | AGTTAAAATAAAAAT[A/G]TTTACAGATATATTC | 23072 |
rs140398568 | in-del | -/A | 0.46137 | 0.133501 | intron-variant | HECW1 | GRCh38.p7 | 7:43258367 | AAAAATAAAAAAAAT[-/A]AAAAAATAAAAAAAA | 23072 |
rs140429273 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43197772 | ACTGGCAACATAACC[A/G]TGGCCCCAGTGACAA | 23072 |
rs140432791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43452304 | GCATGAATCTACTTC[A/G]AATCTGTGCAGTACA | 23072 |
rs140440904 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43348749 | ATATTTTAATTTCCA[A/T]CTTGATTTCGTTTTT | 23072 |
rs140451999 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43493388 | ATATTATCAGATTAC[A/T]TATCATTTATATGGT | 23072 |
rs140452644 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114453 | ACTAAGAAGGGATTA[A/G]AGTCCACATGCCCAC | 23072 |
rs140477093 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43528066 | ATTAATTAACTACTT[C/T]GATTAATTTTGTAGA | 23072 |
rs140487517 | in-del | -/T | 0.248755 | 0.249997 | intron-variant | HECW1 | GRCh38.p7 | 7:43446624 | ACAAATTTTTTTTTT[-/T]AACAGGAGCTAAAGT | 23072 |
rs140503828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43286119 | CATTATTGCCCTTGC[C/T]TTCAAGAGAGGAGCT | 23072 |
rs140505725 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43335530 | AGCAGAAACCTGATC[C/T]ACCAGCACCTTGACA | 23072 |
rs140516607 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523411 | GCCTTTGAGGAGACA[A/G]TGTCAGAAGAGAGAG | 23072 |
rs140517807 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43169135 | CTGGGTAATTACAAG[G/T]GATCATATGCTATTC | 23072 |
rs140522451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126711 | GCCATTTTTTCCAAC[A/G]GCATGTGCTCACTTA | 23072 |
rs140532491 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521895 | AACAACAACAGAAAA[A/G]GAAGTGAGGCGTTTG | 23072 |
rs140542094 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43332288 | CTCAAAATCACAGAC[A/G]CACGGAGCTGGAACC | 23072 |
rs140548924 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43316235 | ACACCAGAAGAAATG[C/T]ATACCACTCAGAAAA | 23072 |
rs140568894 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | HECW1 | GRCh38.p7 | 7:43195091 | GTGTTCCCCTTACCT[A/G]CTGCCACAAGTATGA | 23072 |
rs140569298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43242296 | ATGGGAGTTGAGTGG[A/G]AGAGGGAGGTTTGGA | 23072 |
rs140588860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124234 | AAATTTCATTTTAGA[A/G]GCAAAAGAGAGTGAA | 23072 |
rs140589297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120308 | TATCAGATATCACAC[C/T]CTCAGAAAGGCTTAT | 23072 |
rs140616328 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | HECW1 | GRCh38.p7 | 7:43231939 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 23072 |
rs140619240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43339244 | AACTCCAATTACATA[C/T]GGTGGATCATTCCAT | 23072 |
rs140619933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43238228 | CAGCAATAAAGCGCT[A/G]CATTGGGAGGGATGG | 23072 |
rs140623196 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43313268 | ATTTATTTCTGAAAA[A/C]AAATTGTTCTTGAAT | 23072 |
rs140628936 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43560237 | TAACCATCCTACTCA[A/G]TTTACTGAGTTCCCT | 23072 |
rs140636862 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43164271 | CCATTGGCACTTAAT[A/T]GTTATTATTTTTATG | 23072 |
rs140666592 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43460442 | TGTTCTTGGGCTTTT[G/T]TAAAGGGGGGAGGTT | 23072 |
rs140683061 | snp | C/T | 0.00844564 | 0.0644321 | intron-variant | HECW1 | GRCh38.p7 | 7:43507998 | CAGGGCCACTGCTCA[C/T]CACCCCTTCTCCTTC | 23072 |
rs140687812 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43365170 | CTCCCTTTGCCTGCC[G/T]GTTCTCCTGCAGTGC | 23072 |
rs140705764 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43485668 | TAAACATATCTAAAC[A/G]TAGAAAAGGTAAAGT | 23072 |
rs140706775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405316 | CACCCCTAGGTTCAA[C/T]AATTTGCTAGGAGGA | 23072 |
rs140713803 | in-del | -/TAT | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358812 | GGAGGATCCTTAAAA[-/TAT]ATTCTTTTTTTTTTT | 23072 |
rs140718381 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43465710 | ATCTATCACAGCTGT[C/G]GTTAGCAACTTGTGA | 23072 |
rs140721097 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43245848 | GGTTTCCTGGAAGTT[-/A]AATGCAAAGCTCCTT | 23072 |
rs140721439 | in-del | -/T | | | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562994 | TTTAAAACTTTGATA[-/T]TTTTTTTTTCACATT | 23072 |
rs140743343 | in-del | -/CT | 0.182614 | 0.240747 | intron-variant | HECW1 | GRCh38.p7 | 7:43198726 | ATACAGATTTGCACA[-/CT]CTCACACCCCACACT | 23072 |
rs140755262 | snp | A/G | 0.0726307 | 0.176182 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213539 | CAAGCTCCACCTTCC[A/G]GGTTCACACCATTCT | 23072 |
rs140756619 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43502675 | CAAAAAACAAACAAA[C/T]GAAAAAAAAGATATT | 23072 |
rs140760780 | in-del | -/GATCACTTTTGGTAGTAT | 0.308414 | 0.24308 | intron-variant | HECW1 | GRCh38.p7 | 7:43182740 | GGTATTCAATCTGTA[-/GATCACTTTTGGTAGTAT]GATCACTTTTGGTAG | 23072 |
rs140761004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116366 | ACTTAAACAGAAGAC[A/G]TGAGCACCCTTCTGC | 23072 |
rs140763325 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43185448 | GCTTCTTGCAACTGG[C/T]ATCTGAAGTGGGGCC | 23072 |
rs140777339 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510960 | GACCATGCCTTGCCT[A/G]CTGCCCCGTCCCTGC | 23072 |
rs140778841 | snp | A/C | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43301259 | CTTCTAGTAAAGATA[A/C]GCTTTTCCACGAGAA | 23072 |
rs140782405 | in-del | -/TAAGA | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43355506 | CTATTCTTTGTGATC[-/TAAGA]TAAGTTGTCATCTCC | 23072 |
rs140782974 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43179990 | TAAAATAATCAGACA[A/T]CTCCAGCAACCTTAG | 23072 |
rs140783363 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43219866 | AGACAATATGAGGGG[C/T]GGTATCCTCCCTTAC | 23072 |
rs140788575 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43333809 | TCTGGGTCAGCCACA[A/G]GGAGATAACAGAGTC | 23072 |
rs140796110 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43226255 | AAAGTTCAAATGTTA[C/T]AAACTCTAGCCTTGA | 23072 |
rs140796380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43217000 | GAGGGACCAGCTGTC[A/G]AGGGTTCTGTGGCTC | 23072 |
rs140813469 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43419723 | TTTTTGTTAGAAATG[C/T]TTGTTTCCCAATGCC | 23072 |
rs140816136 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43242651 | GTTGGCGATGTTCAC[A/G]TGGTAACTAAGGCCA | 23072 |
rs140822312 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43546705 | GCACTGACAGAACCA[A/G]TCCAGAAAAGAGGTT | 23072 |
rs140826283 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43173457 | CTAGGGCAGCAGTCC[C/T]CAATATTTTGGGCAC | 23072 |
rs140828554 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43290496 | TTTAACCTCAATGCT[A/G]GTTAGCTGTGCCTAA | 23072 |
rs140832047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43537614 | TATTTTCCTTCAGCT[A/G]TTGTTTTAGATTTGA | 23072 |
rs140833395 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43461175 | CAGCTAGGCAGTTCT[C/T]TCCCAGAATATCTCC | 23072 |
rs140833527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142659 | TCTGTGGTAAATCCT[A/G]TGTGGCTTCTAATTT | 23072 |
rs140833941 | in-del | -/ACACACACACACAC | 0.247447 | 0.249987 | intron-variant | HECW1 | GRCh38.p7 | 7:43250119 | TTTTTTTTAACCAAA[-/ACACACACACACAC]ACGCGCACACACACA | 23072 |
rs140835828 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43337148 | AGGTTGAACTAATTT[A/G]CACTCCCACCAAAAG | 23072 |
rs140849002 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43216086 | TTTTATATGGTCTTT[A/G]TTTTATAAGATGAAA | 23072 |
rs140849525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283109 | CAACCTGGGTGATAG[A/T]GTAAGACTATCTCCA | 23072 |
rs140867237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43182870 | TTCATCAGAGTTTTA[C/T]GGTTTTAAATGTAGA | 23072 |
rs140868789 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43259400 | TCCAAAAAAAAAAAC[C/T]GTTCAATATATAATT | 23072 |
rs140875239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43475041 | GGAAGGTGAAAAAGT[A/G]CTGGGGAAGGAGAGT | 23072 |
rs140876647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144113 | CTGTAAGAGTTTCTC[A/G]GACGTTCCTTGTTTT | 23072 |
rs140890780 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43392095 | TCACCTCATTTTTAG[A/G]TTCCATTATTATTAT | 23072 |
rs140891753 | in-del | -/AAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546628 | TATCAAAAAAAAAAA[-/AAC]AAACAAACTTTAAAA | 23072 |
rs140911173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412023 | GATTGTTTTCTTATT[A/T]CCCCTTCTTGACTTG | 23072 |
rs140931613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43312518 | CAACATTCTTACTGC[C/T]TTGTATTCAACAGAC | 23072 |
rs140936351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43532938 | GGGCCCAGTCAGCCT[C/T]CTTCAAGTTTTCAAG | 23072 |
rs140952654 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43351315 | TTGGCTTTGGTTGTT[C/T]AATGCTCTATTTTTG | 23072 |
rs140989386 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43272773 | TGGAGATTTCCAAAA[G/T]AACTTAAAACAGAGC | 23072 |
rs140997678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43318261 | AAATTTCTACCTGGG[A/T]GTGAAACTTGTTATA | 23072 |
rs141005170 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43463224 | TGACCTCTGCCCAAT[C/T]ATATCAATTACCCGA | 23072 |
rs141006376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128169 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCAAAAA | 23072 |
rs141008987 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440884 | AGAACAATTTTTAAG[C/T]CGGGGCTTGTTGGGA | 23072 |
rs141017471 | snp | C/T | 0.000182402 | 0.00954817 | synonymous-codon, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509110 | CGCATTTGTAGAAAA[C/T]CATCTTGAGTGGTAA | 23072 |
rs141029010 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43484988 | CACTGCAATTCCTAA[C/T]ATAAGTTGACATCAA | 23072 |
rs141037967 | in-del | -/TTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184003 | AGCATTTGCCAATTC[-/TTT]TTTTATTATTATTAT | 23072 |
rs141046065 | in-del | -/CCCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316791 | CCCCTCCCCTCCTCT[-/CCCC]CCTCTCCTCTCCCGT | 23072 |
rs141059268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43380422 | CCATATCGTGCTGTA[A/G]TTTTTCATTCTTTTG | 23072 |
rs141059367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43431271 | CCTGTACAGTCTTCT[A/G]TCCTTCCATGCCCAG | 23072 |
rs141068199 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468538 | ACTTTTTTTTTTTTT[-/T]GGAGACAAGGCCTTG | 23072 |
rs141080141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43397257 | TCACATGGGGCACAA[A/C]TGGCAAAACAGATAA | 23072 |
rs141080216 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358361 | GACAACTTTGAGGTG[A/T]CTTGGAGAATAAGTA | 23072 |
rs141098568 | in-del | -/CA | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43439365 | GCCGGAATTCAGACT[-/CA]CACCTGTGTCTCTCC | 23072 |
rs141099410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428167 | AGATGAAAAGTTTCA[C/T]TTTGCTTCCTCTTCA | 23072 |
rs141105365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43368644 | GGAAGTTTAGATTCT[A/G]TCCTAGCCCAACATT | 23072 |
rs141110262 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298268 | AACTCCATAGAATAT[A/T]TGGAGTTATTAAATT | 23072 |
rs141110666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43504104 | CCTTTTTCTCATTCT[C/T]AAGGCCTGTGGCCCC | 23072 |
rs141112139 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123875 | CTGCTCTCAGTTAAA[C/T]GGCACATATTGTCTT | 23072 |
rs141116512 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43194579 | ATCAGAGACAAGGAC[C/T]TTCTTTTCTTGGCTA | 23072 |
rs141135921 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43475905 | TAAGAATGTAAATAT[A/G]TTTTCGTGACCTAAT | 23072 |
rs141136110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380977 | TGTATGAGAGCTCCA[A/G]TTGTTCCACATCCTT | 23072 |
rs141146575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139271 | AGTGTTTAATGGGGA[C/G]CACCATGGCAAACCT | 23072 |
rs141148937 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43550200 | GGCTGAGGCAGGAGG[A/G]TCATTTGCCCCCAGG | 23072 |
rs141155481 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43428671 | AGCATCACTGAAGAT[A/G]ACAGTTTATCAACAA | 23072 |
rs141163751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43534178 | TCTTTTCTTTCACTA[C/T]CCAAAATGTCCTTCC | 23072 |
rs141174520 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43392990 | TGAGAATGAGAGTAG[A/G]AGAGAAAGACATCTG | 23072 |
rs141198580 | in-del | -/C | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43434392 | TCTTTTCCCATTCTA[-/C]AGGTGAAGATGCTGA | 23072 |
rs141201098 | in-del | -/GGGGG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43535407 | AAGGTCAGAGTGGCT[-/GGGGG]GTAGTTTTCTTCAGC | 23072 |
rs141206691 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43168065 | TGTACGCTTCCTTTC[A/G]GCATTTGTTCAATTA | 23072 |
rs141218697 | in-del | -/AAGTCAG | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43187232 | ATCACAGAAGAGAGC[-/AAGTCAG]AAGTCATGATGTCTT | 23072 |
rs141223551 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517606 | GGTAGAAACCACAAC[A/G]TTATGAGATCCCACT | 23072 |
rs141234795 | snp | C/T | 0.212122 | 0.247114 | intron-variant | HECW1 | GRCh38.p7 | 7:43416238 | CTGTTTGTTAGTTTT[C/T]CTTCTAACAGACAGC | 23072 |
rs141240595 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563962 | TCCGTTGTCAATCAA[A/G]GAGTATACATTATAG | 23072 |
rs141262805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513570 | TCATGATTCCACCCA[C/T]TTCCTTTCTTTCTCG | 23072 |
rs141272180 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43164542 | CTCAGTGCACCCCTC[C/G]TGTGCTCCCCATGGG | 23072 |
rs141279357 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119511 | TTGGCTCTCAGACTT[C/T]TTCCCTTCTTACTTA | 23072 |
rs141279798 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43278925 | TAGTCTCCTCCCCAT[G/T]AGGATTCAAGCTCTG | 23072 |
rs141299554 | snp | G/T | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43274786 | CCAATGTGATAGATG[G/T]GAGTCACACGTGAGG | 23072 |
rs141302755 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160862 | CACTTCTACTGTTCC[C/T]GCCCGCTGTGCTGTG | 23072 |
rs141305195 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43199502 | TATTTCACCAACCCC[A/G]CTGCATTTTATCCTA | 23072 |
rs141310163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43252126 | TACACCTGCGAGCCC[G/T]CTACTCAGCATATAA | 23072 |
rs141310753 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247792 | GAGAGAAAAAAAGAA[-/AAG]AAGGAGGGAAGGAAA | 23072 |
rs141313729 | in-del | -/CCAGTTCCCTGAGA | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43265635 | TTCCACACTAATTCT[-/CCAGTTCCCTGAGA]CCAACTGGGTATCCA | 23072 |
rs141321566 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43180196 | ATGTGACTGTTTGAG[C/T]CTGCTGGTAATGAAT | 23072 |
rs141321973 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132437 | GCCCCTAAATCTACA[C/T]TGGGGGTTGCAAAAT | 23072 |
rs141326440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405096 | TTTTCTCTTTCTTGT[A/G]TTAAGGATATAATCT | 23072 |
rs141328978 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43369701 | CTAGAAAAAAGAGGA[C/T]GTGAAAATTAAATGA | 23072 |
rs141343272 | in-del | -/TCC | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248697 | TCCTCCTCCTCCTTT[-/TCC]TCCTCCTCCTCCTCC | 23072 |
rs141343915 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43338288 | ATAGGGGACTGCAGC[A/G]TCAGTGCTGTGTGAT | 23072 |
rs141363464 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43334514 | ACAAACAACCCTTAT[C/G]CGTTGCAGCAGCTAC | 23072 |
rs141369959 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43451090 | AAACTGGTGGTTTTT[G/T]GGGGGTTTTTAGTTT | 23072 |
rs141371291 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43195998 | CAAATCCAGCACCAC[A/G]TTGGGTCCAGTCGGT | 23072 |
rs141371889 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43399169 | TCTCCAGGCAAGAAG[A/G]GGGTTTGTTTCAGGA | 23072 |
rs141380381 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43491262 | GTAAACCTGGGGAAA[A/C]TTTACTTTTCCTGGA | 23072 |
rs141387211 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43178041 | TTGAGACAGAGTCTC[A/G]CTCTGTCACCCAGGC | 23072 |
rs141388422 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126562 | AAAATTGACCTAACT[G/T]CTGATTTATATGAAA | 23072 |
rs141404354 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43447286 | TCTACACATGGTCAA[C/T]TGAAACTTGGCTCAA | 23072 |
rs141423254 | in-del | -/T | 0.067446 | 0.170804 | intron-variant | HECW1 | GRCh38.p7 | 7:43372658 | TTTTAACATCTATAA[-/T]TTTTTTAAATAAATT | 23072 |
rs141424870 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522788 | CCACAAGAATGTGCA[C/T]GGAGCACAGGGAATG | 23072 |
rs141439385 | snp | G/T | 0.186421 | 0.24178 | intron-variant | HECW1 | GRCh38.p7 | 7:43331239 | GAACATGTGGTGTTT[G/T]GTTTTCTGTCCTTGC | 23072 |
rs141442041 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43286433 | ATCGCTGACTTCTGC[A/G]TTTTCCTTTCTCCTG | 23072 |
rs141442382 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43553568 | CAGCTACTCAAAAGG[C/T]TGAGATAGAAGGATC | 23072 |
rs141444188 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156502 | AATTAATATTTCAGC[A/G]ATAACACAACTGCAA | 23072 |
rs141459704 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43366373 | CCCAAATTCTAGGTC[A/G]TTACCTTTGGCTATA | 23072 |
rs141460250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43361280 | TTCTAATAGAGACAT[A/G]TGCAATCACAGTGAA | 23072 |
rs141460415 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43243250 | GCCTGGCATCTCTGC[C/T]CAAGTCCTGTATGCT | 23072 |
rs141464229 | in-del | -/AGTT | 0.497151 | 0.037632 | intron-variant | HECW1 | GRCh38.p7 | 7:43224667 | CTACAGAAAATAAAA[-/AGTT]AGCCGGCCATGGTGG | 23072 |
rs141465963 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43443161 | ACAGATTTCAAAATA[C/T]GAATGATAAGATGCC | 23072 |
rs141481677 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43264888 | TCGAGAAATAGTTCT[C/T]GCAGTCTGCTTCCCC | 23072 |
rs141491141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43461522 | GCTGCCTTAGTCTTT[A/G]GCAGGCCCCGTTCCC | 23072 |
rs141493947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43422583 | TTCATTAGCCAGGCT[A/G]GTCTTGAACGCCTGA | 23072 |
rs141500502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43280959 | CATGCATTCCCGACA[C/T]AGTATTCTCTTTTCC | 23072 |
rs141502973 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43344440 | TTGTGTTAAGAAGTC[A/G]TCTGTCAATATGACT | 23072 |
rs141532901 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43459201 | TCCTCCCCTATAGCT[C/T]CTGGAATGTGCCTGC | 23072 |
rs141533881 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43304185 | AGCAAGTAGAGCTCT[A/G]GATAAAGCTGCCCTG | 23072 |
rs141534164 | snp | A/G | 0.00016567 | 0.00909986 | intron-variant | HECW1 | GRCh38.p7 | 7:43500787 | ATTTTGCTGAGGTAG[A/G]GGGCTAGGCCTGAAA | 23072 |
rs141542324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43377539 | TGTAGATTAAGACAG[A/G]ACTGGTGCTTTTAGA | 23072 |
rs141543210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43389532 | TACACCCTAAGAACC[A/G]TCAGGGAAAATCTAC | 23072 |
rs141548168 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | HECW1 | GRCh38.p7 | 7:43326423 | TGGGGCTCAACCCCA[C/T]GCCCAGGGAGGCCCT | 23072 |
rs141553346 | in-del | -/G | 0.161596 | 0.233848 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43301198 | CCCCCAACACTGTCT[-/G]GCAGACAGCTAAGAG | 23072 |
rs141555260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43218594 | TCTTGGAAGGCACAG[C/T]AAAGCTGGCTTTGGG | 23072 |
rs141564669 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43437219 | TTCACCTAGTTTCTC[G/T]GGTGTCTTTTCATGT | 23072 |
rs141584255 | in-del | -/A | 0.0912534 | 0.193131 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512171 | GCATCACTCATAAGG[-/A]AACGGAGAAACCAAA | 23072 |
rs141605521 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | HECW1 | GRCh38.p7 | 7:43349386 | ATTTGTTCCAAGGTA[C/T]AGTTTAAGTCCATTG | 23072 |
rs141609352 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43276743 | ACTGACGATTTATAG[C/T]ACGTACAAAATTAGC | 23072 |
rs141627229 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412610 | CCTCCCCCCTCCCCC[C/G]ACCCCACCACAGTCC | 23072 |
rs141644199 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43536625 | AGATTCTGAGCAGGG[A/C]CCTGGGGGCCCTTCA | 23072 |
rs141652785 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43384525 | AAAGATGTTACATTA[A/G]CAAGAAAAAAATACG | 23072 |
rs141662347 | in-del | -/TTTATTTATTTATTTATTTA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159106 | GCATGAATCTGACAG[-/TTTATTTATTTATTTATTTA]TTTATTTATTTTAAA | 23072 |
rs141667714 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43496347 | AACTGTGGACCCAGG[C/T]TGAGAACCCAAATAT | 23072 |
rs141675702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138114 | AGAATAATAACCCTC[A/G]AATTTTTTTCTCTAG | 23072 |
rs141693617 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43170398 | TTTTCCACGAAACAG[G/T]TCCGTGGTCCCAAAA | 23072 |
rs141701728 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43459662 | CCTACCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 23072 |
rs141712229 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43476065 | ATATTACAAAAAAAG[A/G]AGGTAAAAATAGAAG | 23072 |
rs141713764 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43346728 | TAGCCAATTATCCCA[G/T]CACCATTTGTTGAAA | 23072 |
rs141723483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43233424 | TGTTTGCTTTTCAAT[A/G]TCTTAGACACTCATG | 23072 |
rs141740090 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155699 | TTTCTCTGCAGCAAT[G/T]GTCTCTAAGATAATA | 23072 |
rs141741214 | snp | A/T | 0.0283406 | 0.115616 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118523 | AGCAAGTGATTCCTC[A/T]TCCTCTTTCCTGTAA | 23072 |
rs141742273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43194142 | AGGGTATCATGAGGC[A/G]TGTCCCATATGGCCT | 23072 |
rs141748005 | in-del | -/T | 0.359998 | 0.2245 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127883 | TCCTTTTTTTTTTTT[-/T]AAAGACAAGGTCTTG | 23072 |
rs141763008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122305 | TGAATAGTGTCAGAC[C/T]GGAGCGAGAATTGTC | 23072 |
rs141777204 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43340788 | TAGAAATACCATTTG[A/T]TCCCCTGATCCCATT | 23072 |
rs141786094 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43408974 | ATGGAAACGTGCTCC[C/T]ACCAAAGGAACTTGC | 23072 |
rs141791746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43229021 | AGATTTTCCACAGTA[C/T]GAATGAATTATTTTT | 23072 |
rs141796510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43165352 | TATGAATTATGTTAC[A/G]TATCATGAGGTTAGA | 23072 |
rs141803077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529545 | ATCTTCCATTTGACT[A/G]TCCCAAAAGCCTCCA | 23072 |
rs141806025 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43454013 | CACAATACATTCCAG[A/G]TATTTAATGTATTGA | 23072 |
rs141834878 | in-del | -/TATT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43475544 | TTGATAAAAATTAAA[-/TATT]TATTTATTTATTTAT | 23072 |
rs141859556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43261239 | ATTATTGGCATAGGA[A/G]AAGTAGTTTGTCTTG | 23072 |
rs141859783 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43363093 | ACTCCAGATGTTCAC[C/T]TGCTGCTCAGACCAG | 23072 |
rs141867162 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118131 | ATGGAGACTTCATTC[A/G]GGGTCCCTTTTATAT | 23072 |
rs141871048 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512246 | AGGACATTGTCCCTT[A/G]ACACAGGACAAGCCA | 23072 |
rs141872021 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43188340 | AGGAGCTAAATAACT[C/G]CTCCTATGATTGGTG | 23072 |
rs141875722 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375830 | CCCTGGAGGTCAAGG[A/C]TGCAGTGAGCCATGA | 23072 |
rs141879534 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43401399 | GCCAACACATAATCA[C/G]TGTTTTTGATGAAGA | 23072 |
rs141886637 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43481900 | CTGAGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC | 23072 |
rs141903357 | in-del | -/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422369 | TTTTGGTTGTTGTTG[-/TT]TTTTTTTTTTTTTGA | 23072 |
rs141903403 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43228511 | TGCAAAGAACTATGG[A/G]AACACTCAATGTTGT | 23072 |
rs141905511 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524118 | ATAGAGTCTGATCTC[C/T]AGGTACCTAGATCTT | 23072 |
rs141906259 | in-del | -/AG | 0.380724 | 0.213099 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247934 | GGGAAAGAGGAAAAA[-/AG]AGAGAGAAAAAAGGA | 23072 |
rs141912953 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43284620 | TCTACAGTTACCCTG[C/T]TGTACAATAGATCAC | 23072 |
rs141913422 | in-del | -/TAAA | 0.188316 | 0.242271 | intron-variant | HECW1 | GRCh38.p7 | 7:43192506 | ATCAATAAAAATGAC[-/TAAA]TACGTAAAGATAAAC | 23072 |
rs141921389 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43320184 | ATGCCCAGGTGGGAG[A/G]AGAGATGATTCGAAG | 23072 |
rs141921893 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43323991 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCCAGT | 23072 |
rs141930424 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359122 | TGAGCCACCGTGCCC[A/G]GCCCATATCTTTTAA | 23072 |
rs141930441 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43400517 | AAAGTCGAAGACTAT[A/G]ATACTCAAGAGAAAA | 23072 |
rs141938496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244265 | GAGCTCCGCTGTCTA[C/T]GGGTAATTGCTGTAC | 23072 |
rs141940877 | snp | C/G | 0.0364509 | 0.129988 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43249105 | GCTCGCCCTCTGCCC[C/G]CTAGGTGCCGGGCGC | 23072 |
rs141943475 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145416 | TCCTCCCACCTCAGC[C/T]TCCTGAGTAGCTGGG | 23072 |
rs141951458 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43433559 | CTTTTAGGCAGAAGG[G/T]TGCGTGACCCTGTAG | 23072 |
rs141952534 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43540172 | TTTATAGCAGCTATA[G/T]AGTAGGAAACCCTCT | 23072 |
rs141964999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43257490 | GGCCCGAAGCAAGAG[A/G]CATGGGGTTTGGGTG | 23072 |
rs141968610 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43394972 | TCAGAGATGAAATCA[C/T]AGGGAGTCGGAGCTG | 23072 |
rs141976530 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43184390 | GAGTTGGGCAGAGAT[C/G]CCCAGTAGCAGACCA | 23072 |
rs142000457 | in-del | -/AG | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43279118 | CTACCCATTTATTTC[-/AG]ATTCAACATTTGGTG | 23072 |
rs142005175 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43555989 | TGAGTCATCACTGAT[C/G]ATAGCATGCAGCTTG | 23072 |
rs142008144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43477090 | TAGCCCATGAGAAAA[C/T]GTTTTTCTTTTGTAG | 23072 |
rs142009556 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361967 | GCCAACATGGTGAAA[C/T]GCTGTCTCTACTAAA | 23072 |
rs142031272 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520093 | TTAATTATTAGTGGT[A/G]AACAAATGTCTTAGA | 23072 |
rs142038192 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43433276 | TGTAAGAAATACTTT[C/T]CTAACTGTAACATTA | 23072 |
rs142038470 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43480843 | AGCCACCTCCTCCAG[A/T]TAGCAAACATAAGTC | 23072 |
rs142059769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191513 | TTATAACTTGGGTCT[A/G]TCCATCCTTTTCTAG | 23072 |
rs142063224 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43364715 | ACCTAGTTGTCTTAG[G/T]TTTAAAGAATATAGG | 23072 |
rs142069039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515915 | TTGTGAAAGGTCCAA[A/G]TTTATTTTTATGTCT | 23072 |
rs142072892 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121591 | TATAGTGATATTTTA[C/T]ATATCACTATATGTA | 23072 |
rs142085560 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | HECW1 | GRCh38.p7 | 7:43189718 | AAGAAAACTTTTTGC[A/C]CTGGAGAAGAGTTTC | 23072 |
rs142094049 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43484911 | GATAAGTGGAGTGCT[A/G]TGAATACTGGATCCC | 23072 |
rs142102837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43555235 | CGGATTTTTCCTATC[A/G]AGTTTTAGAACATGT | 23072 |
rs142105929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43307400 | AAATTTAGTGATATC[A/C]GTTGATTTCCCATAC | 23072 |
rs142117558 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43231044 | ATGTGTCTGGTGCTA[G/T]TCTTTAGTCCTCTGC | 23072 |
rs142121411 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130001 | ATTTTCAATCTGCAG[G/T]TGGTTGAATCTACAA | 23072 |
rs142136312 | snp | A/G | 0.106987 | 0.205054 | intron-variant | HECW1 | GRCh38.p7 | 7:43253758 | TAAAAATACAAAAAA[A/G]TTAGCCAGGCATTGT | 23072 |
rs142137298 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43493618 | ACTTACATCTTATGC[C/T]TCATTAGGGTCATTT | 23072 |
rs142139013 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43526739 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAACA | 23072 |
rs142142616 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136305 | ATGAGTAGCTTCCCA[A/G]AGCTGTTATATGTGT | 23072 |
rs142142656 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43181546 | CATTCTAACTGGAGT[A/G]AGACAGTATCTCATT | 23072 |
rs142150041 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43322282 | CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAGGC | 23072 |
rs142151105 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43246284 | TTCCAGCCTGCGTGA[C/T]GTAGCAAGACCTTGT | 23072 |
rs142155765 | in-del | -/CCT | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43173813 | AGACTCACAGTATCA[-/CCT]CCACCACCCAGGTGC | 23072 |
rs142156291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149065 | TAATAATTGTGGCAA[A/G]TAAAATCCACAGATG | 23072 |
rs142159119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43545266 | CACCACTTGAATTTT[A/G]TTCCATGGCCATATA | 23072 |
rs142163797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43212437 | TTCACTTTTTAAAAT[A/G]TATAAATTATGTTAT | 23072 |
rs142171339 | snp | A/G | 0.00220149 | 0.0331043 | intron-variant | HECW1 | GRCh38.p7 | 7:43360998 | AAGTCTCATTTCTCC[A/G]TCTTTGGTTAGACCT | 23072 |
rs142181602 | in-del | -/C | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43286724 | CCAACCAAGGCCTCA[-/C]CCCAGAATCACACCT | 23072 |
rs142191392 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43250737 | TTTTATTTGGCTGCC[A/G]GTGCTTTTTGATTTT | 23072 |
rs142192896 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43259199 | CGAGACCAGCCTGGC[C/T]GACATGGCGAAACCC | 23072 |
rs142197374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43479899 | AGAAGAATGATGACC[A/G]GGACACCCACTTAAC | 23072 |
rs142198116 | in-del | -/A | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116179 | CCACCCTCAGTAAAC[-/A]AAAAAAACACGTAGA | 23072 |
rs142206670 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43179042 | TCTTAGAAGTGCCAG[C/G]CCCTTCACAAGTAAC | 23072 |
rs142213465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300238 | TCCAATAGGAATCTC[C/T]TGAGGTAAACCACCT | 23072 |
rs142225487 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43208137 | TCATTTCTCTTCCCT[A/G]TTATTGAAACCCTCA | 23072 |
rs142232356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43362815 | CTTCCACTGCAGGCC[C/T]GGCCTCTTGCCAACA | 23072 |
rs142241026 | in-del | -/GA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43274645 | CCCGGGGGAGGGAGG[-/GA]GAGAGAGAGAGAGAG | 23072 |
rs142254190 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43382584 | TGCCTATAAGCAGGA[G/T]CTTAATCCCTCATTC | 23072 |
rs142258342 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43316181 | TCCACAAAGATCCTT[G/T]CTCTATTATAAACTG | 23072 |
rs142261444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140967 | TTGGTCCTATTGGAT[C/T]AGAGCCCTGCCCTTC | 23072 |
rs142264163 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43289069 | CAATTCCCATCCAGT[C/G]AAAGAATGGAGTGCC | 23072 |
rs142264719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43211169 | TTTAGAGGTGGATGC[A/G]GTCACCTTCCCAGCT | 23072 |
rs142275800 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43430125 | TGAATCACTATACCT[C/G]TGTTCTCACAGACTG | 23072 |
rs142279539 | snp | C/T | 9.94316e-05 | 0.00705024 | missense | HECW1 | GRCh38.p7 | 7:43508073 | AATCAGGTGATGGCC[C/T]ATTCGCGGAAAGAGC | 23072 |
rs142298968 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328573 | AGACAAGACGCAGGC[A/G]TGCAGTCACTTCTCA | 23072 |
rs142301844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43306668 | ATGCCTTTGTCTGCT[C/T]TCTTTTCATTTCTGA | 23072 |
rs142321066 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43373707 | ACTGTGTGCATTCAC[A/G]TTGTCCAACCATCAT | 23072 |
rs142322051 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43342789 | CTGGCACTTTGGGAG[G/T]CGCAGGCAGGCAGAT | 23072 |
rs142323520 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43424702 | ATCAGGAAATATCAA[C/T]AGAGTTCTTGTGATA | 23072 |
rs142371361 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43457063 | TGAGAATTATTTTGT[G/T]GAAAAACTAGGCCCT | 23072 |
rs142374381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43495521 | GCACTCTAAGCTCTT[C/T]AGAGCAAGGCCTTTC | 23072 |
rs142379769 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376053 | ACACACATATATATA[C/T]ACACACTATTTTATT | 23072 |
rs142411287 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43452985 | GGGAGAAGGCAGCAG[A/G]TGATGTGGTTAGCGA | 23072 |
rs142411437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43498344 | GGGCTTCTTTTTCCC[A/G]CAGGGAGGGAGGCCA | 23072 |
rs142426180 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43163933 | CAAGTAATTTATTTA[A/G]TATTTCTAGAATCTC | 23072 |
rs142428537 | in-del | -/C | 0.188631 | 0.242351 | intron-variant | HECW1 | GRCh38.p7 | 7:43530853 | TAACCTCCAAATCTG[-/C]CCCCCTCCTAAAATC | 23072 |
rs142459103 | in-del | -/AG/AGAGAG | 0.221737 | 0.248397 | intron-variant | HECW1 | GRCh38.p7 | 7:43487964 | CTCAAAAAAAAAGGA[-/AG/AGAGAG]AAGAGAGAGAGAGAG | 23072 |
rs142459857 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43198755 | ACTCTCACACACTAT[A/G]GATTTGCACACTCTC | 23072 |
rs142466384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43176722 | ACCCAATCATCTCCC[A/G]AAGGTCTCACTTCTC | 23072 |
rs142481201 | snp | A/C | 0.00374508 | 0.0431105 | intron-variant | HECW1 | GRCh38.p7 | 7:43493224 | TCTAGGTCTTTCCAG[A/C]CATTTTTCCCGGTGG | 23072 |
rs142488038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43534734 | ATCTTAATTGAGACC[C/T]TAACTGTGCCAGGTA | 23072 |
rs142493779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140329 | ACTAGCAGGGAGGTC[C/T]CAGGCCATAGAGGTG | 23072 |
rs142514691 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43332973 | CAAGTGATAGGACTG[C/G]GATGGGAACCAAGAC | 23072 |
rs142530708 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159513 | TTAAAAAAAATTTCT[A/G]AAAAGTAGAACTTGG | 23072 |
rs142532723 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43231087 | TCCAAAATCTGTTGA[C/T]AGCACTATGAAGTAG | 23072 |
rs142535751 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43195409 | CCAGGCCCTGGGCAA[A/G]GCTGGCTGCCTCAGG | 23072 |
rs142535837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157547 | TTACATTTATAAGGA[C/T]AAAATTGATATATTC | 23072 |
rs142536404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225677 | TGATTATGAAACTAT[G/T]CATGCTACCAAAAAA | 23072 |
rs142547365 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43163830 | TTGATGGAAGGATTT[A/G]GACAAGCAAAGATGA | 23072 |
rs142551917 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43345580 | TTTATCCCTCGATCC[A/C]CTCTCACTCTTCCCC | 23072 |
rs142558330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43446006 | CACATGGAAGATTAG[C/T]AATAGATGTTAATAT | 23072 |
rs142570612 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43267264 | TAAATTTCAAAAAGG[A/G]GAAATTATTGAAGGC | 23072 |
rs142579195 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43487845 | GTGCCTATAGTCCCT[A/G]CTATTCAGGAGGCTG | 23072 |
rs142596090 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43226798 | TCCGAAGAGCCTGGC[A/G/T]TCTCCCGCACATGGG | 23072 |
rs142602873 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43282679 | ACTAATAAAGCTGAT[G/T]TTAAACACTTTCAAT | 23072 |
rs142603183 | snp | C/T | 0.100944 | 0.200705 | intron-variant | HECW1 | GRCh38.p7 | 7:43192186 | CTGGTCTCAAACTCC[C/T]GACCTCAGGTGATCC | 23072 |
rs142607340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43503114 | TAGTATCTCCCTGTT[A/G]TCACTTCCTCCAAAC | 23072 |
rs142613876 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159854 | CCGGCTAATTTTTTG[A/T]ATTTTCAGTAAAGAC | 23072 |
rs142619834 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43391537 | CACTCACCTGTGTTG[A/C]TTTCCCCAGCCCCTT | 23072 |
rs142622677 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43328552 | GAGGGCCCAGCCCAC[A/G]TGGGAAGACAAGACG | 23072 |
rs142640265 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43220299 | TGTGTCCTCTCCCTG[C/T]GGGGTCAGGATGCAT | 23072 |
rs142641019 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43294017 | CTGAGGTGGAACAGT[C/T]TCATTTTGAAAACAC | 23072 |
rs142644153 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268497 | TGTCATGACTTGGAC[A/G]TGCTACTGGACCTAG | 23072 |
rs142648317 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377295 | AGGGAAGTTCAGGTC[A/G]ATGAACAAATGGATT | 23072 |
rs142652271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516988 | TGTATAGGGCAGCTC[C/T]GTTATAATCTTTTGA | 23072 |
rs142679130 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43439107 | TGTCACATGCAGTGT[C/T]TGCACTTGCCATTCA | 23072 |
rs142680041 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43309532 | AGAATTGTCTTCAGC[A/G]AAAGAGAAAGACCCT | 23072 |
rs142688431 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43239112 | TTCCAACGTGAGACC[A/C]GACGGCCACGTTTTT | 23072 |
rs142696466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43170074 | TGTTGGGAACTGGGC[C/T]TCACAGCAGGAGGTG | 23072 |
rs142713680 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488432 | AGAGAGAAAGAAAGA[A/G]AGAGAAAGAAAGAAA | 23072 |
rs142713951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43280795 | GACACTTGAAGAAAA[A/G]AACCCCAGCCAACTA | 23072 |
rs142715463 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43326707 | CATATTGGTGTCTTG[A/G]TGACAATTGAGACAT | 23072 |
rs142722046 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43352359 | TGTTTATCTGAAATT[C/G]AATTTTAACTGGGTG | 23072 |
rs142727764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43442799 | GGAAGCCAGGTTGCT[A/G]TCCCCCTGATAGAGA | 23072 |
rs142728786 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43390565 | AAAAAAAAAACAGCA[A/G]AGTTGTGGAGGCAGA | 23072 |
rs142742707 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43388594 | CTGAGGAGGATACTG[C/T]TTCTCAGCCCCAGGG | 23072 |
rs142747363 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43278706 | GGTGTCAGGCTTGGT[C/T]TCCCCTCTGCTTCCA | 23072 |
rs142759542 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43251436 | AGCCTCAGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 23072 |
rs142765904 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43351284 | GCAGAGGGTGCAATG[A/G]ACTCCATAGGGGTCC | 23072 |
rs142766940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43437627 | CTTCCATCATAATCA[C/T]GAAAAACCATATTGC | 23072 |
rs142776528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43179250 | GCTCCAACTTGAATC[A/G]AGCTGTATTATTTGT | 23072 |
rs142785518 | in-del | -/GT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43460560 | TGTGTGCGTGTGTGC[-/GT]GTGTGTGTGTGTGTC | 23072 |
rs142805428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43386938 | CATAAGGCCAAGACT[A/G]CCCACATATTAAGTC | 23072 |
rs142809782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43401945 | ACAGAAGAGTGGCAC[A/G]GCAGAGAAGGAGAGA | 23072 |
rs142810665 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43453761 | GACCTGCACTGCTAT[A/G]ACTTGCCCCAGAATC | 23072 |
rs142843830 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128971 | GCTGCAATATCATGA[A/G/T]AAAATTTTAACAGAT | 23072 |
rs142847040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43524803 | CCGTGTGCTTGTAAT[A/G]TTTGGAAAAGAAGTT | 23072 |
rs142868585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160550 | ATTCATCCATTCTCC[C/G]TTGGTTTGGAAATGT | 23072 |
rs142891234 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43450014 | CTTTTAATAATCTGA[A/G]GCATGCATCCTGTGG | 23072 |
rs142905633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421143 | AATAGATGCACCACA[C/T]AGCATCATCGTTTTA | 23072 |
rs142907079 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43174025 | TAAAATTTTCTTGTA[A/G]AGACAATGTCTTGCT | 23072 |
rs142920740 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248671 | GGCTGCTTTACTCTC[-/CCT]CCTCCTCCTCCTCCT | 23072 |
rs142929354 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125173 | ATGCCATTCATGAGG[G/T]CTCCAGCCTCATGAC | 23072 |
rs142932720 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214713 | GCAGAGCACAGGAGA[C/T]GGCAGGGTGGCTGGG | 23072 |
rs142945584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43288390 | TATTCTTCTCTCTTG[A/C]CATTTTTCTGCAAAC | 23072 |
rs142976447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184654 | GGGCTAAAGGTTGAG[C/T]TGATCACCAATGGCC | 23072 |
rs142976785 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43167850 | TCTAACACACACCCT[C/G]TTTTAAAGAGGAAAC | 23072 |
rs142990359 | in-del | -/GT | 0.0415255 | 0.13798 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523213 | TCTCCATGTTGGCCG[-/GT]GGGGGGGTCTCGAAC | 23072 |
rs142991713 | snp | C/T | 3.31647e-05 | 0.00407201 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43456298 | TTATTAAACACTAGA[C/T]TGGGAAGCTCGAATT | 23072 |
rs142995769 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43532230 | AGTAAATTCCCTTGG[C/T]TGTATCTTGAGAATA | 23072 |
rs142999239 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43210405 | ACAGGATTTTTGCAT[G/T]CCTGGGCCACTGATA | 23072 |
rs143001963 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253014 | GAAGTTATTTAGCCC[A/G/T]GTCATTTGCAAGTCT | 23072 |
rs143010197 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43209525 | ATTTACAAGAGAGCT[-/TC]TCTCTCTCTCCTGTC | 23072 |
rs143014386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550268 | GCTCCAATCTGCTTA[A/G]AACAGCCAGAGCTCT | 23072 |
rs143030407 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298635 | GCATGTACCTGTGGC[A/T]CTAGCTTCCTCAGCA | 23072 |
rs143036120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43470951 | TACATGGACTAGTCC[A/C]TCTCAGTCTAAATAC | 23072 |
rs143038683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43393437 | TTCTGCAACGCATCT[C/T]GAGTGAGAAGTCAGG | 23072 |
rs143041873 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43223520 | GCTACTCGGGAGGCC[A/G]AGGCAGGAGAATCGC | 23072 |
rs143074341 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43330617 | TATGACCTGCTGAGC[A/G]CCACAGAGTCACAGA | 23072 |
rs143083571 | in-del | -/ACAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43345800 | TTCCATCATATATAT[-/ACAC]ACACACACACACACA | 23072 |
rs143094492 | snp | C/G/T | 0.0138972 | 0.0823475 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358917 | GCCACCTCCACCTCC[C/G/T]GGGTTCCAGCAATTC | 23072 |
rs143098305 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519693 | ACAGCAGATCCACAC[A/T]GCACAGTCATATGAG | 23072 |
rs143111405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43219889 | TCCCTTACTACCACA[A/G]AAGGTTCTTTTGTGG | 23072 |
rs143125588 | snp | C/G | 0.021333 | 0.101051 | intron-variant | HECW1 | GRCh38.p7 | 7:43293540 | TAGTCCTAGGAAGTC[C/G]GCATGAAACAACCTT | 23072 |
rs143130603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43220872 | TGGTGCCCCTTGGCT[C/T]TAAAAATGGGCAGGG | 23072 |
rs143134787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43423515 | GCCAAAGTGTTCCTT[A/G]TACTTGTCTGTTAGC | 23072 |
rs143141602 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43441553 | GTGTCTTTTTTTATT[C/T]TCTCTCTCTCTCTGT | 23072 |
rs143148994 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153928 | TGAGATAAATGAGAT[A/G]TTTACTTTTTGAAGA | 23072 |
rs143154344 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130862 | ATTAGAAATGCTCAA[A/C]CTGTATTAATAACTG | 23072 |
rs143162812 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354176 | AATCTCTACACAAAC[A/T]TATCCAATAATAAAA | 23072 |
rs143172998 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43428949 | AGAATACATATATGT[A/G]TAATATATGTATGTG | 23072 |
rs143182425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43239024 | CTGAAAGACAATAGA[C/T]TGGGACAAAACAAAA | 23072 |
rs143183344 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43313495 | GGCATGTGCCACCAC[C/G]CCTGGCTAGTTTTGT | 23072 |
rs143186197 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138983 | CAGACAGACTGGTTT[G/T]TTTGTTTGTTTGTTT | 23072 |
rs143189487 | in-del | -/AG | 0.0103336 | 0.0711337 | intron-variant | HECW1 | GRCh38.p7 | 7:43266760 | ATATCACCTAACAAC[-/AG]AAAAATTCTCAAACT | 23072 |
rs143190502 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43534030 | CCCAAGTTTAATGCC[A/G]GGAAATCAAACTGCC | 23072 |
rs143199948 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43428268 | GAGTGTGCAGTCTAG[C/T]ATGCATAAAGGAGTA | 23072 |
rs143202017 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43351899 | ATTCAGAGGGCTAAG[A/G]CTGGTGTATTTCTCA | 23072 |
rs143205699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43459124 | TATCTCATCCTACAG[A/G]CCTGACTCAATGTCG | 23072 |
rs143207558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43341732 | TTAATATAACCAGTC[C/T]GTAATACAGCATTCT | 23072 |
rs143211670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43471576 | GCTTCAGGAGGACCG[A/G]GGCAAAGAACACGCT | 23072 |
rs143213624 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43425783 | TTCAATAATAGCATT[A/T]ATCCATTTATGAGGG | 23072 |
rs143221315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156250 | GTGCATTAAGTGTTC[A/G]TCAGCTTCATACTCG | 23072 |
rs143236933 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43552450 | TTGACTAAAGCGAAC[A/G]AGTCAGTGGCATTTA | 23072 |
rs143246206 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43337231 | ACTTTTTAAATAATA[A/G]CCATTCTGACTAGTA | 23072 |
rs143246240 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43374417 | CCACGGGAAAAGGAA[C/T]TACTGAATTAGAAGA | 23072 |
rs143252820 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43190629 | TCATCTTTCTATGCT[A/C]TCTCCAAGGACCAGA | 23072 |
rs143254277 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43259807 | TAAAAACACTTTACC[C/G]ATCATCAATCAGTGA | 23072 |
rs143258274 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43454797 | TAAGTTTTCAATGAA[A/G]CTGTTAGTATCTGAC | 23072 |
rs143258702 | in-del | -/TTG/TTGTTG/TTGTTGTTG | 0.343477 | 0.231866 | intron-variant | HECW1 | GRCh38.p7 | 7:43179554 | GTATATTTGCTAAGT[-/TTG/TTGTTG/TTGTTGTTG]TTGTTGTTGTTGTTG | 23072 |
rs143265493 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43151171 | AAGAGGCAGAAAGAT[C/T]TCAGTAATTTGGAAA | 23072 |
rs143268020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43407051 | CTTGTGCAGCATGAA[A/G]TTGTACATGGTCAGA | 23072 |
rs143274027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43547914 | ACAAGAAAGATCACT[C/T]TTTACTGTGATACAC | 23072 |
rs143286368 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376190 | TTAGGACCAAAATAA[A/G]CGTGTAAGATGCCAC | 23072 |
rs143288833 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43309090 | GTGTAGGAGTGAACA[G/T]GGACAGATCAACTAG | 23072 |
rs143293554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43528416 | CACATTAACCTAATT[C/T]AATCCTTATAATCTG | 23072 |
rs143293831 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43202565 | TGAAACCACTGCCTC[C/T]CGGGTTCAAGCGATT | 23072 |
rs143297492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43451052 | TACAGTGTTAACAAA[G/T]ACCAATATGACACCT | 23072 |
rs143306627 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43467702 | GCAAGGAATGGCTCC[A/G]TTCAGGGACATTTCT | 23072 |
rs143319472 | in-del | -/AG | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43358259 | CTTACTGCTTTATTC[-/AG]AGTCCTTCCCTGATC | 23072 |
rs143323475 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant, nc-transcript-variant | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150962 | CTTGCTAAGTAAAGT[A/G/T]GGGGGTGGGCCACGG | 23072 |
rs143327577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43218223 | GATATATTTAGATCA[C/T]GGATTGAATTGTTAT | 23072 |
rs143331891 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43187518 | TATCTATATTTTATT[A/C]TTTTAGATACTATTA | 23072 |
rs143351379 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43436871 | TTTTAAAATTTTTGT[G/T]TATATTGTTTTGAGA | 23072 |
rs143354766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43362433 | ACATGTGCTTTTGAC[A/G]GCTTCGCTGTTTTTC | 23072 |
rs143362874 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43260287 | CTATCTGAACTAAGA[A/T]CAGAAGCGTGAGATG | 23072 |
rs143371060 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43481489 | TCTCTTACAATTACA[A/C]GAAATTAGTCTGAAA | 23072 |
rs143374881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43559751 | TGAGGTAAGCAGGCA[C/T]TCGGTGCTGTCAGAA | 23072 |
rs143395420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512473 | AAAATGCTGTGAAAT[C/T]GGTATTCATATTTTA | 23072 |
rs143396768 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481994 | AAAAAAAAAAAAAAA[-/G]AACTAGCTGGAAGAC | 23072 |
rs143398424 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43200330 | GTAATATGATGCAGT[A/G]TTTTTAAATCTTCTT | 23072 |
rs143414003 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129639 | AAAACAAAAACAAAA[C/T]GGATAAAGGACAAAA | 23072 |
rs143426533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43318938 | GGTGAAGTGGAAACT[A/G]CAAGGGCTCCATAGA | 23072 |
rs143430459 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213031 | TATATCAGTAAAAGC[A/G]TAATGAAATTAGTAA | 23072 |
rs143433096 | snp | C/T | 0.00126639 | 0.0251315 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509139 | AAGCTCTATAATGTT[C/T]ACTTTCTTGTATTTG | 23072 |
rs143437798 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510220 | ACATTCAGGCAGGCT[C/T]CATTCTGATGGTAGA | 23072 |
rs143439452 | snp | G/T | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43113244 | CGCAGCGCCTCCCCC[G/T]CCCCTCAGCGCCCTC | 23072 |
rs143460916 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43243575 | CCACAAACACCCACA[C/T]CAGATCCTTGTTTCT | 23072 |
rs143484151 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43555110 | GGCAGAGGCAAGGAC[A/T]TTAATATAAAAATGC | 23072 |
rs143489857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225003 | AGGCAACTCGGGGCC[A/T]ATTGAGTGTTTTGAG | 23072 |
rs143490390 | in-del | -/TT | 0.497933 | 0.032082 | intron-variant | HECW1 | GRCh38.p7 | 7:43335911 | TTTCTGTCTTTATCT[-/TT]CTTTCTCTCTCCTTT | 23072 |
rs143501188 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43348925 | GGCTCATTTTATGGC[A/C]TATCATATGATCTAT | 23072 |
rs143507135 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158738 | GCTACCTCTCCCTGG[A/G/T]TTCCAGTTACCATCC | 23072 |
rs143516801 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43325762 | TCCCGGATCCCACCT[C/T]ACCTCCCGGGTCAGT | 23072 |
rs143527835 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43240142 | GGTCAGGAGATCGAG[A/G]CCATCCTGGCTGACA | 23072 |
rs143554626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43240933 | CCTGCTGCCCTGTGC[C/T]GAGCACTCCTAGAGG | 23072 |
rs143558132 | in-del | -/GCGCGCGCACACACAC | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302950 | CGTGCACACACACAT[-/GCGCGCGCACACACAC]GCGCGCACACACACA | 23072 |
rs143569200 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43172015 | AGGCACAGTGGCTCA[C/T]ATCTGTAATCCCAGC | 23072 |
rs143590853 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43275755 | CACCCTCCCCCACTC[A/G]CTCCCTGCAACAATT | 23072 |
rs143595275 | in-del | -/AAAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43383830 | AGCCTTGCCAGTAAC[-/AAAG]AGTTGATTAACATAT | 23072 |
rs143597444 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43200190 | TCTCAGTTTCTGGAA[C/T]ATCTACCAAAAAAAG | 23072 |
rs143599918 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43369359 | GCTACTCGGGAGGCT[A/G]AGGCAAGAGAATCGC | 23072 |
rs143618590 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529967 | ATTTATTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 23072 |
rs143624956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43495324 | GTGTCCATGTGTTCT[C/T]GTTGTTCAGTTCCCA | 23072 |
rs143634617 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43490816 | AGGCTGGAGTGCAAT[C/G]GTGCAATCTCGGTTC | 23072 |
rs143634772 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43444086 | CTCTGGCCAGTGAGA[A/T]ACCCTCATCAACCTA | 23072 |
rs143637196 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117927 | CTGATTTATTGGTCT[A/G]AAGCTTGATGCATAT | 23072 |
rs143662721 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43400628 | GAGGGAAGTGCAGAG[C/T]ATATTAAATAAGAGA | 23072 |
rs143674621 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43228465 | CAATATAAATTGGCT[A/C]AGAGAAGGTTGAAAA | 23072 |
rs143676979 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43278954 | TGTGAGGACAGAAAT[G/T]TCTGTCTGTGTTTGC | 23072 |
rs143683073 | snp | C/T | | | missense | HECW1 | GRCh38.p7 | 7:43541203 | GGTCTGGCTCTGATC[C/T]ATCAGTACCTTCTTG | 23072 |
rs143686499 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | HECW1 | GRCh38.p7 | 7:43447956 | CAGGGTGAAACCCTG[C/T]CTCTACTAAAAAAAA | 23072 |
rs143687162 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43410507 | TGGTGGTGGAAGGAG[-/AC]ACACACACACACACA | 23072 |
rs143689094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43473910 | ATAACAAGTAAGTAA[A/G]TAAAGTAAAAAAGTA | 23072 |
rs143691497 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43351401 | AGTATGCAGAGGGAC[A/C]AGTGGTGGGCGATGC | 23072 |
rs143693452 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43391369 | TCATTATTGGGCCAC[A/G]AGAAATAGCAGCCTG | 23072 |
rs143695942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523679 | TTTTTCCTTGAGATC[A/G]AGGGAAATAAATGGC | 23072 |
rs143698714 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43270041 | AGCATTGTTGTAAGC[C/T]CTGTTACTAGAATAT | 23072 |
rs143708202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43346552 | TTTTGGGTTCTTGGT[C/T]GTGAAATCCTTGCCT | 23072 |
rs143713119 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43173290 | AAGAATGGTTTTGCT[A/G]TCTGGTTTCTGGAAA | 23072 |
rs143723940 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43486620 | TTTATTTTTTTAAAG[C/T]AATTACACCTGACAT | 23072 |
rs143727622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380019 | ACATGGGTTATTCCC[C/T]GGCTCAGCCACTTAA | 23072 |
rs143728229 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43469335 | GCACTCCTAGCCCTC[A/T]CGCTGCTAGATGCCA | 23072 |
rs143734637 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43387324 | GAGGATCCAGGTCTT[C/T]CTCTGTGGTCTTTAT | 23072 |
rs143744500 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43283942 | TGCCTTGAGTGTCAG[A/G]AGTGGAACAGCCACA | 23072 |
rs143753896 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43476415 | GTTACACCAACTATC[A/C]TGAGGAAAGAATTCT | 23072 |
rs143768894 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297949 | CATGATAGTACATGA[C/T]GGTGGTCCCAACTAC | 23072 |
rs143770949 | in-del | -/TAG | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156583 | AAAGATAACCTGAGA[-/TAG]TAGGCTGTCATTAGT | 23072 |
rs143772522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43393300 | ATGTCCCTGGCAGGC[A/C]TGCAGCCTCAGGTTG | 23072 |
rs143780762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43222047 | ATTTTAACAAGATCT[A/G]CAGGCCATTCATATG | 23072 |
rs143785540 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123555 | GACTTTAATGAAAAG[C/T]TGTGTCCTTGCCCAT | 23072 |
rs143796008 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480721 | CACACATATATACGC[-/AT]ATATATATATATATA | 23072 |
rs143814578 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43411875 | GACAGCATATTCTTC[A/G]GACTTAATTTCATTT | 23072 |
rs143815180 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43531098 | CATGAATTGCACGCT[C/G]TTCTAAACACATACC | 23072 |
rs143815749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43219305 | CCAGGGCTTTCCTAC[C/T]GGACAAGAAATGTTT | 23072 |
rs143818570 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43342613 | CTTGAGGCTAACTCT[C/T]ACAGAGTAATTATAG | 23072 |
rs143857424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43451162 | TAACACAGTGTTTTC[A/G]GTGCCTCTCAACTTC | 23072 |
rs143862763 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130204 | TTTTTGACATTGTAT[A/T]AGTGTATATTACAGG | 23072 |
rs143879674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43215912 | TCCAAGGACGTATAG[A/G]GCCAGTGTTCAGAGA | 23072 |
rs143882215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43229974 | CCTCCTGTTACAGGG[C/T]ATTGAGGGTTCATCG | 23072 |
rs143886072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129640 | AAACAAAAACAAAAC[A/G]GATAAAGGACAAAAT | 23072 |
rs143897099 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162331 | CATTGGCAGGGCTGT[A/G]CTCCCTCACAAGGCT | 23072 |
rs143905779 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43335299 | AATTAATATTCAAAT[A/G]TCAGAACCAGTTAAA | 23072 |
rs143906566 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43245006 | GCCCTGCTGCCTACT[C/T]ATGCAGAGGGCAGCT | 23072 |
rs143923948 | in-del | -/GGCCAGGGAGCTGCAAG | 0.157642 | 0.232314 | intron-variant | HECW1 | GRCh38.p7 | 7:43226697 | CCTGTGAGGGGAAAA[-/GGCCAGGGAGCTGCAAG]GGCCTGACCCTCCTG | 23072 |
rs143924340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43258712 | GCACTAACTGAAAAC[A/G]TACTTGTTAAATTGC | 23072 |
rs143924783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43175525 | AGACCATTTCATGAA[C/T]ATCAGTGCTGACCGA | 23072 |
rs143926051 | snp | A/C/T | 0.00161625 | 0.0283845 | intron-variant | HECW1 | GRCh38.p7 | 7:43450785 | TTGATGATGTTGCCA[A/C/T]GGCAGTGAATGAATC | 23072 |
rs143946476 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43174879 | CTAACAGCAACTCAG[A/T]TGGAATATACTTACT | 23072 |
rs143948507 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43271942 | CACATTACCTGACTT[C/T]AAACTGTGTTATAAG | 23072 |
rs143950483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244200 | CAGTTGTTACAAGTG[A/C]ATTTGTACCTGGAAA | 23072 |
rs143956368 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43370888 | TAGGGCAATGATATT[-/C]TTTTTTTTTTTTTTT | 23072 |
rs143960482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43384911 | GTCGTTTGGTTTAAT[C/T]GCTATTTTAAAAAGT | 23072 |
rs143975954 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43461984 | ATTTCTGTAACTTTA[A/G]CAATCACTCAGATGA | 23072 |
rs143991088 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43184906 | GAGGAACAGATGAGG[C/G]GAGGTGCCACACACC | 23072 |
rs143998228 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511245 | TGATGTTCTCCCTCA[C/T]GTGGAGAGTATTTGT | 23072 |
rs144009401 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112850 | CCAGTCCCAGGCGCC[C/T]GGTGCACTATGCGGG | 23072 |
rs144012128 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300745 | ACTGATGATGGGCAT[C/T]ATGGTTCATAATCCC | 23072 |
rs144019567 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43491950 | GCTTTCTTTTCCATC[A/G]CTTTTTTACTTTTTC | 23072 |
rs144019806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43395976 | TTTTTCTCTTCCTAG[A/T]ACAGATTACCTTCTA | 23072 |
rs144031877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297613 | GCTGCTCCTGTAATC[A/G]AGATGAAAATTACTG | 23072 |
rs144034136 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43478946 | TTTATCTATGACTGA[C/T]ACTGCTTCATTCAGC | 23072 |
rs144036874 | in-del | -/C | 0.0287284 | 0.116357 | intron-variant | HECW1 | GRCh38.p7 | 7:43499661 | AAGATTAAAAAAAAA[-/C]ATCCTTAATTTTCCC | 23072 |
rs144039030 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43368290 | ATGGGCAGGCCCAGA[A/G]CATGATGCAGGGTTT | 23072 |
rs144040333 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299616 | AAAGATTAGCTGTGT[C/G]GAAAATGTCAGAAGA | 23072 |
rs144041834 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43417343 | GCATGAGCCACCACA[C/T]CTGGCCTCTTCATTT | 23072 |
rs144054779 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43224120 | ACTGTGGAAAAAAGA[A/G]CTTTGATTATTTTAG | 23072 |
rs144061064 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43410931 | GGGTTTATTAAATTT[C/G]TTTATTTTGTGAAAG | 23072 |
rs144071042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43195512 | TAGCCACGCCTCTTA[C/T]GTTACTGCCCCAGAA | 23072 |
rs144080459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43356539 | CTACACACTGACCAC[A/G]TGGCCTAACTGACAT | 23072 |
rs144088276 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43507343 | GTAATATTGTTTTTG[A/G]GACTGGCTACTCTGG | 23072 |
rs144088486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43429697 | GTTCACATGCTCCAT[A/T]TGCTTCTTGCCTGCT | 23072 |
rs144089151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124964 | TTTGGGGTGTTATAC[C/T]AAATACCATAGACTG | 23072 |
rs144108679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521136 | TGGTTTGACGGATGC[A/G]TCTCTCAGAATTCAT | 23072 |
rs144109092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43474406 | GTGAGCCGAGATGGC[A/G]CCACTGCACTCCAGC | 23072 |
rs144117848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222139 | TCTCAGAGCAATTAG[G/T]TCAGAATTTCTGGGG | 23072 |
rs144127285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43552860 | AAGCAGGAGCTTGTA[C/T]ATGCCTTTCTCCAAC | 23072 |
rs144128683 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43470564 | GGGAAGCACAGAGAT[A/G]CACTGTGAGAGTTTT | 23072 |
rs144128937 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153330 | AGAATGGAGATGGGC[A/G]TATGTATTCCCTTTC | 23072 |
rs144135403 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156208 | ATAAAGAAAAACTTA[C/T]TCTTTACAATACTTT | 23072 |
rs144135825 | in-del | -/TTG/TTGTTG/TTGTTGTTG | 0.0512842 | 0.153308 | intron-variant | HECW1 | GRCh38.p7 | 7:43305585 | AAACTGGATAGTGTT[-/TTG/TTGTTG/TTGTTGTTG]TTGTTGTTGTTGTTG | 23072 |
rs144158826 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43263086 | TTATCTGCATTTTCC[A/G]CAATTACTTACCTGT | 23072 |
rs144161847 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150029 | ATCTCATGATATCTT[C/T]TTGCAGTGCAATATA | 23072 |
rs144162715 | snp | A/G/T | 0.00716521 | 0.0594565 | intron-variant | HECW1 | GRCh38.p7 | 7:43189342 | GGGGCCTGAGACTTC[A/G/T]CATTTCTAATTAGCT | 23072 |
rs144164970 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43555916 | GTTAAGTTGAATGAT[A/G]ATTTCAAGAATATAG | 23072 |
rs144184288 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517381 | TCTCCCTTCCCAAGC[A/G]GATACTACCTGGGTG | 23072 |
rs144200666 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122742 | ATAATAAATGTTAAG[C/T]TTCGAGATTCTAAAG | 23072 |
rs144214918 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43254681 | TTAGATATGATATAC[A/G]AAAGTGTATGAGGAG | 23072 |
rs144223216 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43473378 | CACTGATGAAACACC[A/G]AAAGCCATTCTCCAG | 23072 |
rs144226867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43440055 | GGGGCCACTTCTGCA[A/G]TGCTGCCTCCTCCGG | 23072 |
rs144233913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43553336 | TGTCCCCAGTACACT[C/T]AGCCCCGCAATGCCT | 23072 |
rs144268097 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359842 | TAAGGGACCAAGACA[C/T]AGCCTGGTAATTTTT | 23072 |
rs144272112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43317725 | TTAGTGTGAGGGAAG[A/G]GGATGCTTATCAGGA | 23072 |
rs144290707 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43434277 | AGTTCAATAACCAGA[A/G]AGTCAAAAGGAGAAG | 23072 |
rs144315147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43250070 | CTGAATATACGCCAC[A/G]GATGGATGTGTATTT | 23072 |
rs144332129 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162575 | TTACATATGCACCCT[A/T]TTCCCAGATAAGGTC | 23072 |
rs144345534 | in-del | -/TA | 0.172028 | 0.23753 | intron-variant | HECW1 | GRCh38.p7 | 7:43405253 | TTATGATGAATGTTT[-/TA]TATATATATATGTCT | 23072 |
rs144352444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43559491 | TGATTCACAGGTTAC[A/G]AAACGCATTTATGTG | 23072 |
rs144362805 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43290514 | TAGCTGTGCCTAAAC[C/T]CCAGAAGGGAGGGGG | 23072 |
rs144371779 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | HECW1 | GRCh38.p7 | 7:43216263 | TGATTCTTCAGCCTC[A/C]GCCTCCTGAGTAGCT | 23072 |
rs144384642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140752 | GACTGGGCATCTTCA[A/G]CAGAAATTTATTTTC | 23072 |
rs144403349 | in-del | -/GAAG | 0.100588 | 0.200439 | intron-variant | HECW1 | GRCh38.p7 | 7:43237122 | GAAGAAAGAAAAAAA[-/GAAG]GAAGGAAGGAAGGAA | 23072 |
rs144413872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43429777 | ATTTAATTTCCATTA[A/G]TAATAAATAATGGCA | 23072 |
rs144418252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43492507 | AAATGAGGTGAATTT[C/T]ACTGTTTTTAGACAG | 23072 |
rs144440515 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43170866 | TGAAAGTAGGGCGGA[G/T]CAGCACATGTGCAGG | 23072 |
rs144443156 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43266630 | TGAGCCACCGTGCCC[A/G]GCCTCAGGAAATGTT | 23072 |
rs144456716 | snp | A/G | 0.195837 | 0.244062 | intron-variant | HECW1 | GRCh38.p7 | 7:43488390 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAATGA | 23072 |
rs144457628 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336128 | TCTTTCTTTCTTTCT[C/T]TCTCTCTCTCTCTCT | 23072 |
rs144464018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43212536 | CAAAACCAAATCATA[A/T]GCACACAATTACAGA | 23072 |
rs144470603 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43378051 | GTTGTGTTTTAAAGA[C/G]TTGAGTTTAATTGGA | 23072 |
rs144478016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43487489 | ATGTCTGGGGAAAGG[A/C]AGGCCACCAAGGGCT | 23072 |
rs144490670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43310502 | GCAACCATCAGTAGG[A/G]CCAAAGGAATTCCAA | 23072 |
rs144491751 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43205127 | CTCGCACTATTGCCC[A/G]GGCTGGAGTGCAGTG | 23072 |
rs144494191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332295 | TCACAGACACACGGA[G/T]CTGGAACCTCAACCC | 23072 |
rs144499864 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43500414 | CAGAACAGTCTTTCA[A/G]GAGCAATCTCTTACC | 23072 |
rs144501700 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135845 | CTTGCATTTCATTTC[A/G]TTTGATTTCTGAATT | 23072 |
rs144509442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43205879 | GTCCACAGTGCAGGC[A/G]GCTGGGGGCCCCCTA | 23072 |
rs144512842 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43397095 | TTAGGAAGTAATAGA[C/T]GTGAAAGCATGTTGA | 23072 |
rs144516374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425426 | TGGTCACTTGTATTT[A/G]TAAGTAATCCAATCA | 23072 |
rs144522346 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43281311 | TGAGCCCCTCTCTGC[A/G]ACTTGTTGCACCAGG | 23072 |
rs144524841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43220027 | GCTGGGCCAGACTTC[A/G]CAAGTCAACACGGTC | 23072 |
rs144533306 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153038 | AGGATGCGAGAGCCA[C/G]CTTTCCCTATATACA | 23072 |
rs144535451 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43438841 | TAAAGCTTTCTATTG[A/G]TAAACATATACTTAT | 23072 |
rs144550324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43392178 | AATAAGACTCAGTGA[C/T]ATAATGAATTTTAAT | 23072 |
rs144550673 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43262566 | CCTTCAAATGAATCT[A/G]TAATTACTTACTTAG | 23072 |
rs144554534 | snp | A/G | 4.31044e-05 | 0.00464223 | missense | HECW1 | GRCh38.p7 | 7:43445033 | GACAGAGAAGAGCCC[A/G]AGGGGGCTACTCCAG | 23072 |
rs144558734 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | HECW1 | GRCh38.p7 | 7:43340714 | CGTCTGTTGGTGGGA[A/G]TGTAAACTAGTTCAA | 23072 |
rs144562127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43164942 | AGTCATGGCTGAAAG[A/C]AGAAGGATGAATCAG | 23072 |
rs144562578 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521503 | TCAGCCTTGGAATAC[A/G]TCATGGCTGCGGGTT | 23072 |
rs144569362 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416870 | CAGGTGAGGCAATGC[-/C]TCGCCCTGCTTCGGC | 23072 |
rs144576607 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43453846 | TGAGCCCTTCAAGTC[A/G]TGCTGATGCCTGAAG | 23072 |
rs144578343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43372978 | GAAAAGACAAAACCA[A/G]TCAATACTGAAACCC | 23072 |
rs144597015 | in-del | -/T | 0.228253 | 0.249052 | intron-variant | HECW1 | GRCh38.p7 | 7:43355993 | ACTCCGTTAAAAAAA[-/T]AAATAAAATGAAATA | 23072 |
rs144601355 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43535836 | GTTGACTCACTTTTT[A/T]AAAAATATTTTATAT | 23072 |
rs144605382 | in-del | -/CTCT | 0.0353451 | 0.128153 | intron-variant | HECW1 | GRCh38.p7 | 7:43198766 | CTATAGATTTGCACA[-/CTCT]CTCACACACACTCCA | 23072 |
rs144613014 | in-del | -/AAG | 0.256619 | 0.249912 | intron-variant | HECW1 | GRCh38.p7 | 7:43257848 | TATGCAATTAGAAAT[-/AAG]AAGAAGAATAGTGGT | 23072 |
rs144613339 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43425027 | GAGAAACATACAAAC[A/G]GAATTAATACAGCAC | 23072 |
rs144619282 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43217603 | TAATTTCAAATGACC[A/G]TAAAAGGGGGAAGAG | 23072 |
rs144625657 | in-del | -/GGAGAG | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43497346 | TACCATGGTGAAGTT[-/GGAGAG]GGAGGCCCTATCACC | 23072 |
rs144629784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150490 | TTCAAGTGATTCTTA[C/T]GCCTCAGCCTCCTGA | 23072 |
rs144639181 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343112 | GGCTGTGCTGATCTA[-/TC]TCTGTCTAATTCATC | 23072 |
rs144639349 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43546973 | AAACCTGTACAGGCC[A/G]ATATCCTTTCTCCTC | 23072 |
rs144653938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43215546 | TTAACAAATGGTTAA[A/G]GTATTTTTAAACTTC | 23072 |
rs144675837 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511744 | GCCATGTGGCAAATA[A/G]TTTAACAAACAAAAC | 23072 |
rs144679329 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144158 | GTTTTGAAGAATGTT[C/T]ATCAGGTATTTTATA | 23072 |
rs144685860 | in-del | -/A | 0.097727 | 0.198275 | intron-variant | HECW1 | GRCh38.p7 | 7:43478010 | TTTGTTGAAAAAAAA[-/A]GGTAATAACTTTCTC | 23072 |
rs144695602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43556136 | AGAGCAGCGTGCTGC[G/T]AGAGTGTGAAACAGA | 23072 |
rs144721555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43180044 | CCCCAAATCAGTAGA[A/G]GAGTTTCACAACTGC | 23072 |
rs144746823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43274960 | AAGATGTCCTGAGAC[A/G]GGCACTCAGTGCAGA | 23072 |
rs144779596 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43346732 | CAATTATCCCAGCAC[C/T]ATTTGTTGAAAAGGG | 23072 |
rs144787680 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43271054 | ATATACAGGTTTAAT[A/G]CAAATCTAAAAATGT | 23072 |
rs144788849 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43236654 | AATGTAGTCTGGCTC[A/G]GTGAATCTGCATTTT | 23072 |
rs144791744 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43464317 | TGTAGAATAAAATTC[A/G]GTTCCCCCAAGAGAG | 23072 |
rs144800067 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43383284 | ATGATTTATGATCCT[C/T]TGGGTATATACCCAG | 23072 |
rs144834658 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43179061 | TTCACAAGTAACACC[A/G]AGGAAAAAGAAAGCA | 23072 |
rs144850240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43231481 | AACTTAGTGCCTTCA[C/T]GGAGACTCACTGCTT | 23072 |
rs144864252 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43386681 | CCCCACCAGCTTCAG[A/C]TGTGTCACCTATCAT | 23072 |
rs144865440 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307983 | ATCTTATATATTATA[G/T]AACATATAATATATA | 23072 |
rs144865556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43350496 | TTCCTCAGGAATATC[A/G]TTTATATTTAGGTTT | 23072 |
rs144879555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118926 | CATCCCCCATGATGG[A/G]TTTTCTGTTTCTTTT | 23072 |
rs144881673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43403869 | TTGAAATAACTTTAA[A/G]ATTCTATTTTTTCAT | 23072 |
rs144889656 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513180 | GCTCCCTCCTGCCAT[A/G]TGCAATTAATTGCTC | 23072 |
rs144899835 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43337093 | CTAATGGTAGTTCTA[G/T]TTTTAGTTATTTGGA | 23072 |
rs144902180 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43348230 | ATCTAATTCTTCTTG[A/G]TTTAAGCTAAGAGGG | 23072 |
rs144916847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421505 | AGAGCAAGCCACAGA[C/G]TGGGTAAAGATGTTG | 23072 |
rs144923622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43504428 | TCCTTTCCTTTCTAA[C/T]GTCTTTCCCTGATGC | 23072 |
rs144952919 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43463235 | CAATTATATCAATTA[C/G]CCGACAAATAAAACT | 23072 |
rs144961003 | snp | A/C/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43418264 | AGTTTGCATTCAAAA[A/C/G]CACCAGGGTCTTAGA | 23072 |
rs144965847 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519709 | GCACAGTCATATGAG[G/T]CATAAAAAAGACTGA | 23072 |
rs144967392 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124066 | AAGCATCAAGCTCTA[A/G]GATAGAAAACCTTCA | 23072 |
rs144969541 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43442813 | TGTCCCCCTGATAGA[A/G]AAGCTCCTCTTCATT | 23072 |
rs144972278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43541627 | CAATTTTCATGCAGA[A/G]TCCCTGAGTCAATAG | 23072 |
rs145016960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43237288 | ATTTCTGACCAAAAT[A/G]AAATGTAAATCACTG | 23072 |
rs145025046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43168244 | TTAATTCAGACCACA[A/G]TTATATGTTCAGCCT | 23072 |
rs145036479 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43564022 | TATTTACTGAGACAG[A/G]ATGGAATCTGTAAGT | 23072 |
rs145041977 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43480796 | AGGGAGTTTCTCTCC[A/G]GAGAAACTGGGAAGA | 23072 |
rs145043763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43525255 | TGAAAATTAACAAAA[C/T]TGGAACTATTATTTA | 23072 |
rs145047546 | in-del | -/TCA | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43418712 | CTTACCTATCTATAT[-/TCA]TCATAAGTTAATATT | 23072 |
rs145049151 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293220 | GCGAGACTATGTCTC[-/A]AAAAAAAAAAAAAAA | 23072 |
rs145050532 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43232544 | CTGCAGCTTTCCTTC[C/G]TCTTGTGGTTTGGGC | 23072 |
rs145057927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43164819 | TTAGAAAGGAGATGC[C/T]GAGCATGCAGCCGCG | 23072 |
rs145071489 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43197447 | AGCCCCCTGCAAAGC[G/T]ATGCGTCCTGGGTGG | 23072 |
rs145080794 | in-del | -/AAAAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43285793 | ACCCCATCTCAACAA[-/AAAAT]AAAATAAAATAAAAT | 23072 |
rs145099342 | in-del | -/TTG | 0.352721 | 0.227922 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268755 | CTCCTGACCTGTGTT[-/TTG]TTGTTGTTGTTGTTG | 23072 |
rs145104158 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43387823 | TTGATTGACTAGCTT[A/T]TGCTTCACGTTTTTC | 23072 |
rs145111652 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43338296 | CTGCAGCGTCAGTGC[G/T]GTGTGATGCCCTGTT | 23072 |
rs145112737 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43288446 | TAAGTTGAACACCCT[C/T]CTTAAAGAGAAAATG | 23072 |
rs145120683 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43291119 | CAGAATGCTTGTTCC[A/G]TGGTGCTGCAAAGAA | 23072 |
rs145122103 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43405227 | GTGGTGGAGGCAATG[G/T]TAGTCACTATTTTAT | 23072 |
rs145133686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43193912 | TGAATGCCCCCCACA[A/G]GAGACAGCTTTGCAG | 23072 |
rs145141704 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43399375 | ACTCACTAATTTTGT[A/G]CTTCTAAGGCAAAAG | 23072 |
rs145154166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123316 | CAGGAGCTTAGAAAT[C/G]ATCGTGACATTCTTG | 23072 |
rs145159835 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43334544 | CTAATCTAAGCCTTG[C/T]TCCTTCTCTCTAAGC | 23072 |
rs145169532 | in-del | -/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43416869 | CCAGGTGAGGCAATG[-/C]CTCGCCCTGCTTCGG | 23072 |
rs145185151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522924 | TCCAAAAACAGCTCC[A/G]TGGTGGGGATGTTAT | 23072 |
rs145187076 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43447502 | AAAGGTTAAGAAGCA[A/C]CTACATGCTTCACTA | 23072 |
rs145191903 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43255444 | TCTCTACCAAAAATA[C/T]AAAAATTAGCTGGAT | 23072 |
rs145200494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207615 | TCTTTCAACATACCT[C/T]TCCCTATCCTTCCCT | 23072 |
rs145201744 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | HECW1 | GRCh38.p7 | 7:43308867 | CCTCAAGTGATCCAC[C/T]TGCCTCAGCCTCCCA | 23072 |
rs145208051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332151 | GGAAGAACTCAGGAG[A/T]GATTTTCATCTACAC | 23072 |
rs145220026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43538679 | TAATTATTGACCCTC[A/G]GTTTCTTAATCTGCA | 23072 |
rs145227701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43461552 | CTGCCTTGGTCAAGG[G/T]CACACACTTGGGCAG | 23072 |
rs145228288 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43423214 | TGAGCAGCCCTAAAG[A/G]CGGCATTATTTCCCC | 23072 |
rs145238526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43245627 | TCATAGGGGATTTTA[C/T]TCAGTGATCCAGGAA | 23072 |
rs145244481 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43366610 | TTTGGAAGACACCTC[A/G]ACTTTATAATAAATG | 23072 |
rs145247867 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43463878 | AAGCCTCCCACCCTG[C/T]CTCATGGGGAGCAAT | 23072 |
rs145263624 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43544615 | TAGAAATTTGTCCTA[C/T]CGATACATTAACACC | 23072 |
rs145268417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43252223 | GCCTTCCCCTGCTAC[A/G]TGGGTCTTTCAGTAG | 23072 |
rs145273304 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43285964 | CAAAGGCCAGTGGTC[C/T]AAACACAAGAACTAG | 23072 |
rs145287876 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360133 | TCATTGTCTCACAGA[C/T]TGTAAATAATGGAGC | 23072 |
rs145291642 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224906 | GTGGAGGGAGTGGCT[-/G]GGGAGAGGCCTGGAA | 23072 |
rs145294313 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43183841 | TAGAATTTTTCTGAA[G/T]ACTGGAAGAATATAT | 23072 |
rs145310933 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43483990 | TGAGGTGACAAAGAG[A/G]AAACAAAGGGCAGCC | 23072 |
rs145341515 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43480943 | TATACTCTGAGAAAC[A/G]TAACTATTTCCAACC | 23072 |
rs145357389 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43181039 | GATAACCACTATTCT[A/G]CTCTCTTCTTCTATG | 23072 |
rs145361730 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302669 | CTCCCTTTCTCTCCT[A/G]TATGGTCCGCAGGGC | 23072 |
rs145364216 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43548301 | TATGCAGGTCATCTG[C/T]GAGTTTTTTCAAATT | 23072 |
rs145366264 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43422904 | CCGAGAGTCGTCACC[C/T]GGAGATAAATCGCAG | 23072 |
rs145368700 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522656 | CCTCAGTCCTCCCAC[A/G]GGCCAAGAGGGAAAA | 23072 |
rs145369684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43492601 | CTTCAGCCACCTCTT[C/T]CCAAAACATATGCCA | 23072 |
rs145370086 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126533 | TAAATGTTTACTAAC[C/T]AGCCCTTTAAGAAAA | 23072 |
rs145374967 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327995 | TATTATTATTATCAT[C/T]ATTATTTTAGTTTTA | 23072 |
rs145379836 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43470745 | ACACACATGCTCACA[-/AC]CACACACACATAAAT | 23072 |
rs145392592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43418179 | GGGACATCAGTCATA[C/T]GGGATTAGGGCCCAC | 23072 |
rs145402019 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43544466 | ATCAGAAAATTTACC[A/C]GTATTTTGGGATGGT | 23072 |
rs145404308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148519 | GTTAGCTAATATTTG[C/T]CCTGCCCTTTACATA | 23072 |
rs145418931 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43535314 | TGTGCAAAACCCAGA[A/T]GGAACTATGAGAAAT | 23072 |
rs145425545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43238287 | GCCATGATGCTGGCA[C/T]CAGAGTGGGTGCTGT | 23072 |
rs145434857 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159337 | ATCCTTCCCCCAGCC[C/G]CCAACCCCCCGACAG | 23072 |
rs145439469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43554877 | AGTGACCATCCTTTG[C/G]GATGGAATTCTTTCC | 23072 |
rs145452957 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43367796 | CCAAGGGTGATATAA[A/G]TTGATGGTTAGATAT | 23072 |
rs145454467 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43211654 | ATAAACCTGTGTTCA[A/T]AATAACCCTTCACAA | 23072 |
rs145454820 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43475395 | GGCTTAAAATAAAAT[A/G]AAGACTTAGAAACCA | 23072 |
rs145456651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43309348 | CTGCCCTGCTTACCC[C/T]GGACAAATGTCATCG | 23072 |
rs145459785 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43351507 | AGGGCTAGACGTGTC[G/T]GAGCTCAGACTTTTA | 23072 |
rs145460728 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43500005 | CCAATGTGGCATCAT[-/A]AAATTTTCCATCAGG | 23072 |
rs145468903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142395 | TCTTAGAAATGTATT[C/T]ATGCACAGAATCTAG | 23072 |
rs145480095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427576 | GGTTTCTATCAGTAC[A/G]TAACAAATTGCCACA | 23072 |
rs145493390 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43537379 | ATACCTAGACACACT[A/G]TCTTAGATCCAGAGA | 23072 |
rs145494487 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43234116 | TTTACAAATTACATG[C/T]AATACCGCCCTGCCA | 23072 |
rs145501105 | in-del | -/GAGA | 0.0603597 | 0.1629 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161581 | TCTCTGGCTCTGACT[-/GAGA]AAGATATTTCAAATA | 23072 |
rs145507822 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43272351 | ACCTATTAAACTAAA[C/G]AGCTTCTGCATGGCA | 23072 |
rs145519297 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43424548 | AAATGGCTTGAGCCC[A/G]GGGGGTCAAGGCTGC | 23072 |
rs145527802 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43259871 | ATCCTAGAATAATGA[C/G]AGAGAGAATGGGCCA | 23072 |
rs145533059 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43186458 | GGATCACGAGGTCAG[A/G]AGATTGAGACCATCC | 23072 |
rs145535536 | in-del | -/TGGT | 0.278664 | 0.248351 | intron-variant | HECW1 | GRCh38.p7 | 7:43533620 | CAGAAGATGCCATAG[-/TGGT]TGGTTAGAAGAGGCC | 23072 |
rs145600568 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43315587 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 23072 |
rs145601732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43268036 | ACTTGCCACTTCATA[C/T]TGGTGCTAGAATCCC | 23072 |
rs145607033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43194486 | CAGAAAGCCACTCCT[A/G]CCCCAAAAAAAGAAA | 23072 |
rs145608534 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43212667 | ATTATCTTGTTTATA[G/T]AACTTACTTTAAAAT | 23072 |
rs145612235 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43465390 | CGGAGTCGGCCACAG[A/G]CTGACCTGAGATGGC | 23072 |
rs145630607 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | HECW1 | GRCh38.p7 | 7:43481751 | GCACTTTAGGAGGTC[A/G]AGGCAGGCAGATCAC | 23072 |
rs145636533 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43560250 | CAATTTACTGAGTTC[A/C]CTTTCACTCAAATAT | 23072 |
rs145643281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43311706 | GTTTTCGTGTGATGA[C/T]GGTGACTGAGTTGCC | 23072 |
rs145652589 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43199109 | CACACTCTCTCTCTC[C/T]ACGGTTTTCTCCAGG | 23072 |
rs145661184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43378996 | TGCTTATGGGGGGGC[A/G]GTGTGCCCTTGCTCA | 23072 |
rs145661529 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127087 | TAGAAATGATCAAGC[C/T]TAGTGAGGACGGCAT | 23072 |
rs145664262 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43357817 | TATATCCCAATTACA[C/T]TCATTTGATCTTTAC | 23072 |
rs145674509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332596 | GCAAGCTGATCACCA[C/T]GGTGTCCAATTACAC | 23072 |
rs145685040 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242361 | ATGAATTCTAGAACC[A/C/G]TTAGGAGGTAGGAGC | 23072 |
rs145695702 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43501557 | AATGTTTTGCTGGGC[A/C]GGTGGCTCATGCTTA | 23072 |
rs145695886 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43426378 | AGTATAAAAGGTGAA[A/G/T]GTCAAAAGTCTTGCA | 23072 |
rs145698909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124291 | GTTGGTATAAATTCG[C/T]AAATAGCTTTTGAGG | 23072 |
rs145700187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375948 | GACTTGCCATGGTAA[A/G]GATAACATTTGAATG | 23072 |
rs145704917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43195215 | GAAAAAAGAAAGAAG[C/T]GTTAATGGTATGGTG | 23072 |
rs145718007 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269625 | GAAAGGCAAGACCAT[C/T]CATCTGGGAATACCC | 23072 |
rs145718183 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43172364 | AAAAAATAGAAAAAA[A/G]TTTTCTATTTTTAGA | 23072 |
rs145737212 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43312733 | GCTGAGGCAATTATT[C/T]TTATGAAAGTTTCAC | 23072 |
rs145740867 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43203846 | TTACAATCCTTTTGC[A/G]GTTGTATACCCCACT | 23072 |
rs145745658 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43379744 | TCCCCCCATTTAGAT[C/T]GTTTTCTCAAATGTC | 23072 |
rs145750622 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43206966 | CACTTGGCATTTTGA[A/G]TATATTATTGCATTA | 23072 |
rs145760332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43333960 | AGTTTAGCAACTCCT[C/T]CTCCCTCCACTGGGA | 23072 |
rs145767219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427211 | AATAACAGTTTCCCC[A/T]ACTATGATCAATATA | 23072 |
rs145771964 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43502981 | CAGAGTTAGTATCAT[G/T]CAGTACTGCCGTAGG | 23072 |
rs145773615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43324510 | GAGAGATTGGCTCTA[C/T]GAAACGTTCTCATAT | 23072 |
rs145775060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43327605 | ATACCTCGTACTCAT[A/G]TTGGTCTTCCCTTCG | 23072 |
rs145783879 | in-del | -/TGT | | | | | GRCh38.p7 | 7:43389620 | TCACATTGTTGTTGC[-/TGT]TGTTGTTGTTGTTGT | 23072 |
rs145787833 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:43388049 | CCATTTGATGCAAAA[C/G]AAAACTGAGCATTAG | 23072 |
rs145791364 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155639 | CTATTTGATAAATTT[G/T]CTGAGTGTGTACCTC | 23072 |
rs145791739 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519143 | TATAATCCTCTATTT[C/T]ACAAATGAGGAAACT | 23072 |
rs145797032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43368589 | TAGATAATTTACCCA[A/G]GCCCTACTCACAATC | 23072 |
rs145805704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43342251 | AATGTTAGATGCCTC[A/G]TCAATGAACATTATT | 23072 |
rs145808410 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43254157 | CAGATTAGATGAACA[A/T]TTGCCTGGGAAGCGT | 23072 |
rs145812651 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43446759 | ACGCAAGGAAATTGG[C/T]AGAGAAAAAGAAACA | 23072 |
rs145824602 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513308 | TGCTCTCCACGACGC[A/G]TGAATGCTGCTTGTT | 23072 |
rs145829884 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43384619 | CAGTGAGGGGGAAAA[C/T]GTTTGCCTTTAAAAA | 23072 |
rs145829885 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43436456 | AGGCAGGCTGAGTCC[A/G]AAAAGGGAGTCAGCG | 23072 |
rs145837806 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562857 | TGAATCCCTGAGTTC[C/T]GTACTGTTCTGTTTT | 23072 |
rs145849190 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43455920 | TCAGGAGAATTGCTC[A/G]AACCCAGGAGGTGGA | 23072 |
rs145850768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43442338 | TTGATGAGTTTATTG[A/G]GTCATAATCCATGGT | 23072 |
rs145852139 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375819 | GATTGCTTGAGCCCT[A/G]GAGGTCAAGGCTGCA | 23072 |
rs145865375 | in-del | -/GT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361058 | TGTTCTTGTGCGTGC[-/GT]GTGTGTGTGTGTGTG | 23072 |
rs145868487 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43497608 | ATAAGATGGAACAGG[A/G]GCTATGCAGGAGACT | 23072 |
rs145900634 | snp | A/G | 0.021333 | 0.101051 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563649 | CGAGGTGGGGAGATC[A/G]CTTGAGGTCAGGAGT | 23072 |
rs145904518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510981 | CCGTCCCTGCAACCA[A/T]CCTGGCTTTGTGGCC | 23072 |
rs145905244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43433472 | AGATTTTTCTGAGAA[C/G]CAAGGCTAAGACCCA | 23072 |
rs145924973 | in-del | -/CT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335971 | TTTCCCTCTCTCTCT[-/CT]TTCTCTCTCTCTCCT | 23072 |
rs145926244 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43494684 | AAATTTTGCTAATTT[G/T]TGTGCATTTATTAGA | 23072 |
rs145944241 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43373885 | ATATAGGAGGAATCA[C/T]ACAGTGTTTGCCCTT | 23072 |
rs145946445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43306758 | GATAAAAACTGACAG[A/C]GCAGAATCTTTTGTC | 23072 |
rs145955746 | snp | A/C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43420768 | TATGGTTACACCGTG[A/C/T]ACTACCACTTTGCTG | 23072 |
rs145959021 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43495976 | GTCTCATTTTAATCA[C/T]TAGAAAAGGTTTTTT | 23072 |
rs145970173 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43540048 | GAGTCAATAACACTA[A/G]CATGTTATTTCATGG | 23072 |
rs145982047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43417375 | TTTCTGAAGACCTGG[A/G]TTTTCCTCTGATATC | 23072 |
rs145985504 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43228534 | AATGTTGTTGAGTTT[A/G]GGGGAGAAGAACACT | 23072 |
rs145991249 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160623 | TTTTGGAGTTTCTTT[C/T]GTTCCATTGATCTGT | 23072 |
rs145996676 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43556794 | ATCTGGGGTCACAGA[C/T]TGAATGTAATTTCCA | 23072 |
rs146010020 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158229 | CAATACAGGTTGACC[A/G]ATATGGGTGGTTATT | 23072 |
rs146029826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43265683 | TTCAAATCAATTCTG[G/T]CACTCACTCCTGGAG | 23072 |
rs146038869 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377452 | TAATTAATCTCAGGT[C/T]CTAGTAGAGCATTAG | 23072 |
rs146040905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43309591 | CACGTACATAAAAAT[C/T]TTTATCTTAGGCTCT | 23072 |
rs146048192 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43206009 | CCCTGCCACTTCCTC[C/T]CCTGGACACTGAAAT | 23072 |
rs146057292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43173695 | GCAGTAATGCTTTCT[C/T]ACCTGCAGCTCACCT | 23072 |
rs146066435 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43327118 | GATGTCTCAATCTGT[G/T]CTACAATAAATACTT | 23072 |
rs146082046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515116 | GAGAATAATTGGCTG[G/T]CAGAGAAGAGGAGTG | 23072 |
rs146083311 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43437736 | ATCAAGTATGATGAG[G/T]CTTTGGTGGCATTCT | 23072 |
rs146092901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43560483 | GGTAGGGGTTAGGGA[C/T]AGTTCCCCAAGGACT | 23072 |
rs146094227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118312 | TTGACATCCATTTAA[C/T]GTGCATGGATGTTCC | 23072 |
rs146094294 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43435247 | TTAGAAGATATATTA[C/T]AATACACTCCAGAAT | 23072 |
rs146113861 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43178795 | CAGAGCCGCTGTGGC[A/G/T]TTCCTCAACTCCAGC | 23072 |
rs146115765 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43283370 | TGTGTGAGAATCCAG[C/G/T]TGTCTTCTGTTAAAC | 23072 |
rs146133559 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43175287 | CATTCAGAATCCACT[C/G]TCAGCAATTTGTAAG | 23072 |
rs146134017 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43215183 | ATTACCAGTGACTGT[A/G]TAGGCACCGCCTAGT | 23072 |
rs146152118 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43210553 | GATGGCTGCAAGCCT[C/T]GTGTTCGCTAACCTG | 23072 |
rs146162571 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43330671 | GGTGGCCATGTGGGG[A/G]CTATGGGCTTTGTCT | 23072 |
rs146163053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43281592 | TCAGCTCTTCTTTCT[C/G]TCAGTCCACTCTCCC | 23072 |
rs146165905 | in-del | -/CTTT | 0.420892 | 0.182472 | intron-variant | HECW1 | GRCh38.p7 | 7:43431880 | TCCCACCGACACTTG[-/CTTT]TTTTTTTTTTTGAGA | 23072 |
rs146167484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43393790 | TGAAGAACCAAAATA[C/T]GTATGCTTTAAAAAG | 23072 |
rs146171239 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43225072 | CTGTAGCAAAGGTGT[C/G]GGGGAAGATGACAGG | 23072 |
rs146187600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43344686 | TGTGTGTTTCTTGCT[C/T]TTTCGTCTATATTTT | 23072 |
rs146203649 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43459389 | CTTTCACAAATATTT[A/C]CTGAAAAGCAGAAAA | 23072 |
rs146208480 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43530975 | CGTCTACAGTTTAAA[-/G]GGTGAACTTGTTGGC | 23072 |
rs146215048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530666 | CTCTATTGAGCTTCA[A/G]ACTTTATTATCAAAA | 23072 |
rs146215630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43455018 | TGCTCTTCTATGTTT[C/T]GCTCAGACGTGAACA | 23072 |
rs146232169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121711 | GCAGAGTCCATCACT[C/G]AGTTTCCTAATAGGA | 23072 |
rs146235484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191538 | TTCTAGCTCTAAGTA[A/G]CACATTTTTGCCATC | 23072 |
rs146242117 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516695 | TCATGTGTCAGTTAA[C/T]GACAGGGATACCTCT | 23072 |
rs146250652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118633 | TTATTCATAATTCCT[C/T]GTGCCATCAAAACTT | 23072 |
rs146254081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189026 | AGGGTGAGGCGCACT[C/T]GGCTAATCTTACACT | 23072 |
rs146270567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43306025 | TCAGCCTCCCAAAGT[A/G]CCAGCATTACAGGTG | 23072 |
rs146271652 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43222889 | CCCATCTTATGACCT[A/G]TTTCACCTGTGCATT | 23072 |
rs146272544 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43229128 | CATTTAATTTGTATT[C/T]GCTTTCTGGTAAATT | 23072 |
rs146281785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300355 | GACAGTTAGAGCTAG[A/G]AAGAGCACAAGAGTG | 23072 |
rs146287428 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43419947 | CTGTATTTGTCCCGA[C/T]TGGCTAGCAACTTAG | 23072 |
rs146303238 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43346445 | CAATATGTGGGTTGT[A/G]TGTTTATTCTCCTGA | 23072 |
rs146307707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359216 | GGTTTATGTTTAGCT[A/G]CATATAACAGAGATC | 23072 |
rs146324475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43477754 | GAAACCACTTCCTGT[A/G]TGAGTTTTTATAAAG | 23072 |
rs146345324 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43391375 | TTGGGCCACGAGAAA[G/T]AGCAGCCTGACCCTC | 23072 |
rs146347396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43209816 | TGAGAGGCGGGCATT[C/T]CAGAAGAGTGAAGGG | 23072 |
rs146361366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43342997 | ACCACTGCACTCCAG[C/T]GTGGGAGACAGAGCA | 23072 |
rs146373278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136540 | CTGGCAAAAACGGGT[C/T]ACTTCTGGAAGCACT | 23072 |
rs146386526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43251383 | AGCGCGGCCTTGGCT[C/T]ACTGCAACTTCCGCC | 23072 |
rs146390596 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43326602 | CCCTGCCATAATTAG[A/G]GGGCTGTGAATTAGG | 23072 |
rs146400863 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43362927 | GCTCAAGGCTCGTAG[A/G]GGAGAGGAGTTCCTC | 23072 |
rs146401856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43321623 | AGATGTTCATTCAAT[A/G]TGGCATGTCAGAAAG | 23072 |
rs146404474 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43245419 | AGTTTTTAAATACCA[A/G]GCAGTTCCTTCTGAG | 23072 |
rs146407370 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43437387 | ATGCTCCAATAAACA[A/T]CCCTGTTAAATGTAT | 23072 |
rs146409336 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150035 | TGATATCTTCTTGCA[A/G]TGCAATATATCTTAT | 23072 |
rs146428634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43185403 | CGAGGGGTAAATAGT[C/T]GGAACTGTCTCAATT | 23072 |
rs146448409 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43184026 | ATTATTATTATTTTT[A/T]TTTTTGAGACAAAGT | 23072 |
rs146450445 | in-del | -/CAGG | 0.0130921 | 0.0798413 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508911 | GAATCTGGGTGCAAA[-/CAGG]TCCCCCCACCTCCGG | 23072 |
rs146453778 | snp | G/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514316 | CTTTTTTTTTTTTTT[G/T]AGATGGAATTTCGCT | 23072 |
rs146465584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43368372 | CAAGCCTTTTATTTC[C/T]TGTAAGCAAATTTAA | 23072 |
rs146470983 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297618 | TCCTGTAATCGAGAT[G/T]AAAATTACTGCCCAG | 23072 |
rs146471789 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43457304 | TGAAATTGCACCCAC[A/C]TGCTGTCTTGCTTTC | 23072 |
rs146476821 | in-del | -/CA/CGCACA | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43275708 | GTTCTTATGCGCACG[-/CA/CGCACA]CACACACACACACAC | 23072 |
rs146483257 | snp | C/T | 0.00266203 | 0.0363859 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508927 | AGGTCCCCCCACCTC[C/T]GGGCACAGAATGAGC | 23072 |
rs146493439 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43503377 | GTTGTAGAGATTGTC[C/T]CAGCCTGATAATGTG | 23072 |
rs146503581 | in-del | -/AAT | 0.0399052 | 0.1355 | intron-variant | HECW1 | GRCh38.p7 | 7:43542183 | CTGTACCCATTAAAC[-/AAT]AACTTTCCATTTCTC | 23072 |
rs146507523 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43427683 | CTCGGCTCAGGATCT[C/T]AGACGCTGAAACCAC | 23072 |
rs146515735 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153451 | AGTTACATTCAACCC[A/G]TACATTATTTTAAGG | 23072 |
rs146518989 | in-del | -/GTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190095 | AAATTTTTGTTGTTG[-/GTT]TTGTTGTTGTTTGTT | 23072 |
rs146520980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550002 | GGTGCTTAGCAATCT[A/G]CTTAGAGGTCGGGTG | 23072 |
rs146534272 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43167995 | ATACCCCTCACCAAC[A/T]CCACACCACCAAGTA | 23072 |
rs146553057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43278922 | TTGTAGTCTCCTCCC[C/T]ATTAGGATTCAAGCT | 23072 |
rs146564951 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43274627 | AAATAAACTCAGGAA[C/T]GCCCCGGGGGAGGGA | 23072 |
rs146568983 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43387071 | GGTACTGAGGCAGCT[G/T]CCAGAACTGTGTTTT | 23072 |
rs146571434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43199448 | TTCATTAACAGTTGA[A/G]TATTTACATTATTCT | 23072 |
rs146589147 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43383227 | TTGCTATTGTAAATC[A/G]TGCTACAATAAACAT | 23072 |
rs146590628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43317964 | GTACATTCTATATTC[C/T]AATGAAATTACCTGT | 23072 |
rs146616206 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43372037 | ATGTTGGCCAGTCTG[A/G]TCTTGAACTCCTGAC | 23072 |
rs146616771 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43446973 | GTATGGACATTACTC[A/G]ATAATTACAGCATAA | 23072 |
rs146627629 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43368599 | ACCCAGGCCCTACTC[A/C]CAATCTCTAACCTCT | 23072 |
rs146634094 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43171488 | TGGCCAGGCTCCAAG[A/G]AAAGACGACCCTCAG | 23072 |
rs146653152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43183116 | TGTGAGGGTAAGTAC[A/G]GAGTTGTGGGGAAAA | 23072 |
rs146657746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43498846 | CTTAAAAAAAAAGAT[C/T]TCCATACCAAAAGGT | 23072 |
rs146666387 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440885 | GAACAATTTTTAAGT[A/C]GGGGCTTGTTGGGAT | 23072 |
rs146671439 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295925 | AAAAACTCAAATCTA[C/T]AGACAAATTGCTGCT | 23072 |
rs146672160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43221151 | TTACTTGGATCCCTT[A/G]TCAGTTAGTAGGGTT | 23072 |
rs146687517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43410165 | CTCCTTGCAAGACTT[C/T]GCATTTTCTTCCTGG | 23072 |
rs146690856 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43217646 | AGTGTAATAAGATTA[A/T]ACAACAGACAGCTTT | 23072 |
rs146692636 | in-del | -/AA | 0.0414363 | 0.137845 | intron-variant | HECW1 | GRCh38.p7 | 7:43355618 | CTAAAAATAAAAAGC[-/AA]AAAAAAACATACTAC | 23072 |
rs146708964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43338184 | ACTGCTGCTCTTGTC[A/G]TTGGCCTGGGAGACA | 23072 |
rs146713816 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514072 | GCTCTCCAGATACTG[C/T]AACCCACAGTGGCCA | 23072 |
rs146714595 | in-del | -/TATT | 0.279726 | 0.248226 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120632 | TGGATAAATCCCCTC[-/TATT]TATTTATTTATTTAT | 23072 |
rs146718643 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119876 | CCATCCCCGTCTAAG[C/T]GCTAGTAAGCTTTCC | 23072 |
rs146719833 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43387464 | CTTGCTTCTGCCTGT[A/G]TGTTTATCTAATTCC | 23072 |
rs146736688 | snp | A/C | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512481 | GTGAAATTGGTATTC[A/C]TATTTTATAAAATTT | 23072 |
rs146746009 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43383434 | TTTCTCCACAGCCTC[A/G]CCAGCATCTGTTGTT | 23072 |
rs146751231 | in-del | -/G | 0.112631 | 0.208878 | intron-variant | HECW1 | GRCh38.p7 | 7:43211473 | GGATTGATCATCTCT[-/G]TCCTCAGGGAACTCA | 23072 |
rs146753212 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114071 | AAGAAGATATTATTT[A/C/G]ACGTTGCTGTAGTTT | 23072 |
rs146755513 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43185284 | TGTCTCCTCCATCTA[A/G]CTGTTCACCTGTATC | 23072 |
rs146763417 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509760 | GGCACTTTCCTGCTG[C/T]ATCACCACATGCCTG | 23072 |
rs146773554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126710 | TGCCATTTTTTCCAA[C/T]AGCATGTGCTCACTT | 23072 |
rs146794487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43241339 | GGTTCCATCCAGGTT[C/G]TCTTTGGTGGGGTGG | 23072 |
rs146797078 | in-del | -/CTTC | 0.497855 | 0.0326773 | intron-variant | HECW1 | GRCh38.p7 | 7:43335784 | TTTCTTTCTTCCTTT[-/CTTC]CTTCCTTCCTTCCAT | 23072 |
rs146803835 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43355799 | ATCGAGACCATCCTG[A/G]CCAACATGGTGAAAC | 23072 |
rs146811848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43237628 | GTTAATATGTGTAAA[A/G]CAAGATGAGCATTTA | 23072 |
rs146812190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43282011 | GTTTCCTTTCCAGCT[A/G]TCATAGAGCAATGTG | 23072 |
rs146822216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43186739 | ACATTTAGATATGCT[A/T]AGATGCACAAATACT | 23072 |
rs146824545 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43279453 | ATTGCAAATCCTCTC[A/G/T]GTGAGCTGCAAGGTT | 23072 |
rs146829445 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43351411 | GGGACCAGTGGTGGG[C/T]GATGCCTTAGAACTC | 23072 |
rs146856390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117460 | CAGGAGTCAGAGCTT[C/T]ACAACCTCCTTACTC | 23072 |
rs146858328 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43485537 | ACCTAGATGGTATAG[A/C]CTACCACACACCTAG | 23072 |
rs146858623 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43531981 | GTGACATCTGTAGTG[C/T]GGCCCTGTGCCCGGA | 23072 |
rs146868792 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43405275 | TATATGTCTTTCACA[C/T]TCTAATAAGTCAGGA | 23072 |
rs146871324 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43202088 | TGATGCTCCACTTAC[C/T]CATTTAACCCTCAGA | 23072 |
rs146876508 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130241 | ATCCCTTACCAAAAT[G/T]CTTGGGCCTAGAGTG | 23072 |
rs146886001 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43527947 | CCTGGAGAACTAATG[A/G]CTGAGGCTCAGACAA | 23072 |
rs146894963 | in-del | -/TCT | 0.0444908 | 0.142359 | intron-variant | HECW1 | GRCh38.p7 | 7:43200647 | ACGAAATAAAGCTCT[-/TCT]GCTGCCAATGTTTTG | 23072 |
rs146900846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184425 | ATAGCTGTGATACTA[C/T]GAAATATGTATTTGG | 23072 |
rs146900979 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43227064 | TATAATCTGGAAGTC[A/G]ATGCCTCTCTCATTA | 23072 |
rs146918613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43243376 | GGGATGGCACTTCTT[C/G]AGTCTTTCCCATCTG | 23072 |
rs146923137 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | HECW1 | GRCh38.p7 | 7:43174152 | AGCCTTAAATGAGTC[C/T]TGATAGGTGGAATTT | 23072 |
rs146923526 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43286537 | TTTAAAGGAATATTT[A/G]GTAAAAGTGCTGGCA | 23072 |
rs146931737 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358447 | TGTGAAAGAACTATC[A/G]AGAAAGTGACTCAGG | 23072 |
rs146933598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283529 | GAACCAATATAAATA[G/T]TTTGCATGTTTTGCC | 23072 |
rs146944804 | snp | C/G | 0.116838 | 0.211584 | intron-variant | HECW1 | GRCh38.p7 | 7:43475962 | CTTATTGTACAATCG[C/G]GTCTAGTAGTTTTCC | 23072 |
rs146954604 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43393026 | ACCTCAAAGCTCTTA[A/G]TTTAACTCCAAGAGC | 23072 |
rs146954692 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43352953 | ACAGTGTAGGAAGGT[A/G]GGGGGGCAGGGAAGC | 23072 |
rs146964231 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43388847 | AGCCCACTGCCCAGC[C/T]TTACCTGTGCCAGTG | 23072 |
rs146967351 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518042 | TCTACTTTGAAAATA[C/T]GTGAAAAAAAGGAAT | 23072 |
rs146967969 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43471326 | AACTCACTAAACAGT[A/G]GGGTGGCCATAGCTC | 23072 |
rs146978909 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138538 | TGTTGTTATAAAAAC[G/T]CCTTGCTTTTCTGTC | 23072 |
rs146996013 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133254 | AATATATACACATTT[A/G]TATATAAATGAATAA | 23072 |
rs147000661 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43528549 | TCATTGAATTGAAGA[A/G]CAATACTAAGTATGT | 23072 |
rs147007707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247206 | ATTTACTGCCTTAAG[A/G]TAGAGGAATGAAGGG | 23072 |
rs147011884 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43178069 | GGCTGGAGTGCAGTG[G/T]CATGATCTTGACTCA | 23072 |
rs147028318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43261368 | TTGAAGAGGGCAGAA[C/T]CTTTTTCCTGAGGAG | 23072 |
rs147028678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43187585 | ATTACTAATATTCTT[A/C]TGTTGTTTGTGTGAA | 23072 |
rs147042264 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43371976 | AGGTGCCCACCACCA[C/T]GCCCCGCTAATTTTT | 23072 |
rs147050688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43493449 | GGAAGGACAGAAAGG[A/T]AACAAAATAGCTTCC | 23072 |
rs147051363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43419089 | TTGGGCTGAGCTTCT[A/G]TACATCGTTTGGGGC | 23072 |
rs147051716 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43369180 | GAGACAATTTAGGGC[C/T]GGGCGCAGTGGCTCA | 23072 |
rs147072430 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | HECW1 | GRCh38.p7 | 7:43490448 | ACACTTCAAAATTCT[A/T]AACTATTTTAAAGCC | 23072 |
rs147073648 | in-del | -/A | 0.078151 | 0.181571 | intron-variant | HECW1 | GRCh38.p7 | 7:43495279 | CCCCCATTCCCCAAC[-/A]AGGCCCCGGTGTGTG | 23072 |
rs147100892 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155940 | CCACTTAGACTGGCA[A/G]CAGTCTACATTTCAC | 23072 |
rs147105564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43552682 | ATGTAGTCTTTCGTG[C/T]CTGGCTTCTTTGACT | 23072 |
rs147109571 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43264662 | CATCCTGGCTAACAC[A/G]GTGAACCCCGTCTCT | 23072 |
rs147109776 | in-del | -/CCCTTTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316763 | TTCTCCTCTCCCCTC[-/CCCTTTT]CTCTCCTCCCCTCCC | 23072 |
rs147116893 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43190348 | TGAACTCCTGACCTC[A/C]TGATCCGCCCACCTT | 23072 |
rs147133498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43165531 | TGCTTACTCTGTGGA[A/G]TTTAGATAGATTTGA | 23072 |
rs147141850 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43277288 | CCCACTGCCACCTGC[A/C]GCCATGACGCTGCCT | 23072 |
rs147149334 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43200405 | CATGCATGTCACTCA[A/G]TTAGTCAAATGATCA | 23072 |
rs147164447 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43319828 | ATGTTGGCCATGCTG[A/G]TCTCGAACTGCTGAC | 23072 |
rs147166045 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43197658 | TGGTAAGACAAGGAT[C/T]AGCAGGACTCTGCCC | 23072 |
rs147183027 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43259161 | GGAGGCAGAGGAGGG[G/T]GGATCACCTAAGGTT | 23072 |
rs147197266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369548 | GGGAGAGAACACCTT[A/G]ATCTTTGGCAGCACT | 23072 |
rs147197487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332188 | GGTACAGTGAAATTG[A/G]ATCTCTACAAAAATA | 23072 |
rs147206705 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43367317 | CAATACTTAGCTAAC[C/T]AGCACTAAAAGGAAA | 23072 |
rs147212228 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43490906 | AGGATTACAGGCATG[C/T]GCCACCATGCCTGGC | 23072 |
rs147221387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43169722 | TTGAGACGGAGTCTC[A/G]CTGTCGCCCAGGCTA | 23072 |
rs147225359 | in-del | -/A/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43345851 | ATATACACACACATC[-/A/AT]ATATATATATATACA | 23072 |
rs147245342 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43502161 | CTTGTGACTCTGAAT[C/G]GATTGCACACCACTT | 23072 |
rs147248944 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43219436 | CAGACAAAACCCCTC[C/G]GATACCGAGCTAAAG | 23072 |
rs147253417 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152503 | CATTATATTGCTCTT[C/T]ATTCTTTTTTATAGA | 23072 |
rs147270594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148529 | ATTTGCCCTGCCCTT[C/T]ACATATGCAGAAACT | 23072 |
rs147270629 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | HECW1 | GRCh38.p7 | 7:43340551 | ACTGTGCAAGCAATA[G/T]CCCCAGGGATCAAAA | 23072 |
rs147272483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43216082 | GTCATTTTATATGGT[A/C]TTTGTTTTATAAGAT | 23072 |
rs147280719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43335481 | GAGAACACAGCAAGA[A/G]GGCAGCCATCTGCAA | 23072 |
rs147293043 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43467147 | CAGATCTAGGTGCTG[C/G]AGTCACAAAGACAGA | 23072 |
rs147302687 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43348047 | ACAGAATGAATTAGA[A/G]AGGGTTCCTTCTTTC | 23072 |
rs147302810 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43384967 | ACCTCACATGCTTAG[A/C]TGAAAAGAGCTAACT | 23072 |
rs147312699 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43382234 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 23072 |
rs147316246 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511269 | TATTTGTGGTGCATC[C/T]TGGAAACGCAATTGC | 23072 |
rs147318662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43462744 | ACACATCCTGATGCC[A/G]CTGCCAGGCATCTCA | 23072 |
rs147328892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43507798 | AGTTCCATATGATGG[A/C]ATGCACGAGAAGTGT | 23072 |
rs147343557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125214 | CAAAGGCTCCTCCTC[C/T]AAGTATCATCACACT | 23072 |
rs147349324 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521545 | TTTTTCCAAAATTCA[C/T]AGGTTGAAACTTAAC | 23072 |
rs147360129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43170248 | TTACTGTATATATTA[A/G]CATGTAATAATATAT | 23072 |
rs147372512 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43235434 | TATTCTTTAAAACTG[C/T]GGAATAAGAGAGGCA | 23072 |
rs147376312 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43166555 | TATTTTAAGAAAAGA[C/T]AGGGGTTAGTCACAT | 23072 |
rs147378147 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43280818 | GCCAACTATATCCTC[A/G]GGTGGACAATAACAC | 23072 |
rs147385260 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | HECW1 | GRCh38.p7 | 7:43350046 | TTTAGCAGTTCTTGT[A/G]GTGGTGGTTTGGTAA | 23072 |
rs147387802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43277570 | CCTTGCCCTTTGCCA[C/T]CTGCTAGGATGTCTT | 23072 |
rs147398465 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43486549 | CTCATGATCCACCTG[C/T]CTCGGCCTCCCAAAG | 23072 |
rs147408665 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43363875 | GCAGAACCACATTTC[A/G]CTTATACTTTTTGCA | 23072 |
rs147409004 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43407903 | GCAACTCAGGGATCT[G/T]GATCAAGTCCATCCG | 23072 |
rs147418661 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43402719 | TAAGCAGAAAGTAGA[C/G/T]AATGGAATTGCCTTC | 23072 |
rs147421341 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43482873 | TCACACCACTGCACT[C/T]CAGCCTAGGCAACAG | 23072 |
rs147431809 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43524876 | AGCTCCTGTGTCCTG[C/T]AGAGGGGCATGAAAT | 23072 |
rs147443047 | in-del | -/GACAC | 0.251859 | 0.249993 | intron-variant | HECW1 | GRCh38.p7 | 7:43440086 | GGTGTCCCACCGTGG[-/GACAC]GTTAGGAGCAGAGTG | 23072 |
rs147449126 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147967 | TTTAGTGATAGTGGG[C/T]AATTTGCAAAGCTCA | 23072 |
rs147466094 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43184757 | TTTACAAAGAGAAGA[A/G]GTTTAGTTGGCTCAT | 23072 |
rs147481906 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43182116 | TCTCTCTTAACTCTG[A/T]TGATTATTTCATTTG | 23072 |
rs147482434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43255361 | CCCAGCACTTTTGGA[A/G]GCTGAGGTGGGTGGA | 23072 |
rs147482495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298692 | AATTACTTTCATTGT[C/T]TCACTTTCCTTTTAA | 23072 |
rs147492015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43293906 | GACAAGCAGCGACAT[C/T]AGATTTTCGTAGGAG | 23072 |
rs147495818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43366547 | GAATCCACAGGTTGC[C/T]GACTGATGGGACCAG | 23072 |
rs147505741 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43429452 | GGGCAGATCTTCTCC[C/T]ATGACCAGACTCCAA | 23072 |
rs147525678 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43350797 | TTGGATTTCCTTGCA[G/T]TGGGCTTCGCCCTTC | 23072 |
rs147528280 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43471666 | AATTTTATAGAGATT[G/T]CATGTGTGCCTCAAA | 23072 |
rs147528575 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43426215 | TACATCTGTTTATAT[A/G]TAGATACACTTTCAA | 23072 |
rs147538284 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151947 | CATATCCTAATAATA[C/T]GTTCTAATTTCATGA | 23072 |
rs147538579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43467827 | AGTGAGGCAGTGACC[A/G]CACTAAGCTGGAGGT | 23072 |
rs147544655 | in-del | -/TATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307877 | TGGTAATCATTTCAC[-/TATA]TATATATATATATAT | 23072 |
rs147556874 | snp | A/G/T | 0.300421 | 0.244863 | intron-variant | HECW1 | GRCh38.p7 | 7:43361860 | TTAAAAAAAAAACAG[A/G/T]CCAGGCGCAGTGGCT | 23072 |
rs147561059 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43484403 | AATATGAGACTCAGC[A/G]ATCATCGATGGGTTA | 23072 |
rs147570364 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43559312 | AAAGACCCGTGCAGA[A/T]CTCCAAAACATCCAT | 23072 |
rs147570865 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43480839 | CTGCAGCCACCTCCT[C/G]CAGATAGCAAACATA | 23072 |
rs147593035 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43555175 | CTGTACTTCTGCAGC[A/G]TATCACTTGATACTT | 23072 |
rs147593831 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43475980 | CTAGTAGTTTTCCCT[A/T]AAAAATCAAGAATAA | 23072 |
rs147604700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43211691 | GGCGTTCCCCCTTGC[C/T]TCCCTCAAATTTTGC | 23072 |
rs147615227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43255716 | GGTGCAGGAGATGAC[A/C]TGATGAGCCAAGCCA | 23072 |
rs147618386 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138737 | GCAACAGTTTTAGGA[C/T]GGAGTATTCCAAAGC | 23072 |
rs147621008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207709 | TTTTAGTTTCCAGGT[A/G]TGAATGAGAACATAT | 23072 |
rs147629589 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328554 | GGGCCCAGCCCACGT[C/G]GGAAGACAAGACGCA | 23072 |
rs147641471 | in-del | -/GGG | 0.470132 | 0.118498 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247882 | GAAAGCAAGCAAGAA[-/GGG]AGGGAGGGAGAGAGG | 23072 |
rs147644509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439797 | CTGAAAGCAAGTACC[A/T]GAGGTGGAAAAGGGT | 23072 |
rs147652429 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43364629 | TGAAGACAGACAGGC[A/G]AGGCCAGCAGAAGGG | 23072 |
rs147652523 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43323966 | TTGAACCAGGGAGGC[A/G]GAGGTTGCAGTGAGC | 23072 |
rs147662215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375996 | ACTGGTTGAGGTGCA[C/T]ATATATAATCATATA | 23072 |
rs147697879 | in-del | -/AACA | 0.0648419 | 0.167978 | intron-variant | HECW1 | GRCh38.p7 | 7:43219666 | AACAGAACAGAACAG[-/AACA]GACAGGGATTTTCAC | 23072 |
rs147699927 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43493486 | AAATTATTTATGTAC[A/G]GCACTGTATAAATTA | 23072 |
rs147707462 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162893 | TCTCAACAACTCTAT[A/G]AAGAGGCAACTATTG | 23072 |
rs147709703 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43559516 | TATGTGTGTTCTGGC[A/G]TTGATCCTCCCCATA | 23072 |
rs147724156 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159828 | GGGACTACAGGTGCC[C/T]ACCACCACGCCCGGC | 23072 |
rs147725570 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43272479 | AAAACTTAATTGAAC[A/C]AGCAAAAAACAACCC | 23072 |
rs147733618 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43346259 | TAGTGATGTTGAGTA[A/T]TTTTTCATATGTTTG | 23072 |
rs147747815 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43460237 | CTACATTAGACATTG[C/T]GGTTCTAGGGGTTTA | 23072 |
rs147756548 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43379159 | GCAGGCAGCATAAGA[C/G]TGTTCCTTTAATCTT | 23072 |
rs147756564 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43342647 | TTTTGGTTAAAATTG[A/C]TTTTCTTGGGGTTTG | 23072 |
rs147765315 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43392833 | TGAGCTATAGTCTCC[A/G/T]GACTGCTGAAACAGA | 23072 |
rs147766038 | snp | C/T | 0.00560097 | 0.0526224 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445224 | CCCCTCGTGCTACAG[C/T]TCCTCGTGCTACAGC | 23072 |
rs147778361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517567 | AAATATCCCTTGCTA[C/T]ATCTGCAGAGTCTTG | 23072 |
rs147778979 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122869 | ATAAACACATGCATA[A/T]AATTTTTAAAATTCT | 23072 |
rs147789311 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | HECW1 | GRCh38.p7 | 7:43440362 | ATCCTCCTTCGATTC[A/C]TTGGCCTGTAAAATC | 23072 |
rs147795658 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119454 | CGATTGATCTCAACT[A/G]AATTTTGACCTTTAA | 23072 |
rs147801516 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513429 | AGAAACCCCTGACAG[C/T]GTGTCCTTCCTCTGA | 23072 |
rs147807972 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43231068 | CCTCTGCATTTATTT[C/T]CCCTCCAAAATCTGT | 23072 |
rs147812766 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43180113 | TAACATTCCCTTTTA[C/T]GCAAGATGCACTTTG | 23072 |
rs147829405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43178040 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG | 23072 |
rs147829630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43290604 | TCCTCTGGGGTCATC[C/G]TGGCCAAGAGGGGGT | 23072 |
rs147839678 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43286420 | TAGTGCAACCAGGAT[C/T]GCTGACTTCTGCATT | 23072 |
rs147860708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43397210 | AACCTGGGAAGAGAA[A/G]CAGCTATTCAACTCT | 23072 |
rs147868025 | in-del | -/CTCACA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198770 | AGATTTGCACACTCT[-/CTCACA]CACACTCCACACTCA | 23072 |
rs147871927 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43346517 | TCCTAGGTATTTATC[A/T]TTGTTTTTATTGCAT | 23072 |
rs147874885 | in-del | -/AC | 0.180383 | 0.240111 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508590 | CACCCACATACACAT[-/AC]ACACACACACATGCA | 23072 |
rs147875853 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43463484 | AAAAGAACTTGAATC[A/G]TCTTAGAGATACTTG | 23072 |
rs147883985 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43536549 | GAGGTCTCTCTTGTG[A/T]AGAGGAGTTGAAGGG | 23072 |
rs147885686 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43460471 | TTGTGTAGTTGGCTG[A/T]TTGGTTTGGCTTGGT | 23072 |
rs147885821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141594 | GCCTCCGCCTCCTGG[A/G]TTCAAGCAGTTCTCC | 23072 |
rs147902498 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138113 | CAGAATAATAACCCT[C/T]GAATTTTTTTCTCTA | 23072 |
rs147907517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43533399 | ACAAACCACCTGGCT[C/G]TCAACCTACAGGTGG | 23072 |
rs147912539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43252089 | ACAGAATATTTCCAA[A/G]TGTGCATCACTATCA | 23072 |
rs147917513 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123415 | CTAGGTCTGCTTGCC[A/G]AGAGACCACTGCTGT | 23072 |
rs147918925 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43193916 | TGCCCCCCACAAGAG[A/T]CAGCTTTGCAGGGCC | 23072 |
rs147935276 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43311143 | GAGATACAGTCCTCT[C/G]AGATTGGATTTTATT | 23072 |
rs147939424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119928 | TGCCCATCTGCAGTC[C/T]GTTCCCTATACAGCA | 23072 |
rs147952398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43231577 | GGTGCCAGAGACATA[A/C]TTCCCCTGGTTTTCA | 23072 |
rs147959225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421804 | CTGCTGGTGAGGTGT[A/G]GAACATAGACTCTCC | 23072 |
rs147967880 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327992 | TATTATTATTATTAT[C/T]ATTATTATTTTAGTT | 23072 |
rs147969387 | snp | C/G | 0.176219 | 0.238865 | intron-variant | HECW1 | GRCh38.p7 | 7:43348424 | TCTTGGTTAATCTTG[C/G]TAATGGTCTGTCAAT | 23072 |
rs147979680 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43465554 | GATGCAGAACTGACC[C/T]GTTGTCACTTCTGAC | 23072 |
rs147988758 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510591 | AATGCTCACTTATAC[A/G/T]CACATATACATATGT | 23072 |
rs148018536 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43280870 | GGGTTTGAGGAACAG[A/G]GAGAAGGCAGTTAAG | 23072 |
rs148052193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43234610 | ATCTTTGAAGCTTTT[C/T]CTGGAGACCCAGGGA | 23072 |
rs148056765 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43165312 | GCAGCCATGTGCATA[C/T]AATTTCCAACTTTAG | 23072 |
rs148063576 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43349222 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 23072 |
rs148064419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43453854 | TCAAGTCATGCTGAT[G/T]CCTGAAGTTCCATTT | 23072 |
rs148070312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43178077 | TGCAGTGGCATGATC[C/T]TGACTCACTGCAAAC | 23072 |
rs148072144 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43276174 | AAGAAATGATCTTAC[A/G]TAACAACTATGCCAG | 23072 |
rs148087403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43187819 | CTCCAACATTTAGAG[A/G]TAGATGGGAGCTCTA | 23072 |
rs148092687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118106 | TGTGCCCATGATGAC[A/G]AATGCCATCATGGAG | 23072 |
rs148095352 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43400920 | GAGGCTGCCAGCATT[C/T]TTTGGCTCATGGCTA | 23072 |
rs148104393 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43228495 | ATGTACCGTCAGGAG[A/G]TGCAAAGAACTATGG | 23072 |
rs148104564 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43334983 | CAATATGAATTTTCT[A/G]TAACACAGAACATAA | 23072 |
rs148112972 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127472 | AGGTTGCGGTAAGCC[A/G]AGATTGCACCACTGC | 23072 |
rs148118307 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523815 | CCCCCAATTAGTGGG[A/G]TGTAAGGAGGCAAGG | 23072 |
rs148120174 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43448270 | ACTGACAACTATACA[A/G]GCTAGTATTCTTTTC | 23072 |
rs148124253 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43346553 | TTTGGGTTCTTGGTC[A/G]TGAAATCCTTGCCTA | 23072 |
rs148132173 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43540051 | TCAATAACACTAGCA[G/T]GTTATTTCATGGAAA | 23072 |
rs148147200 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43476771 | ACTTAATATTATACC[A/T]AAATAAGTTTCAGAA | 23072 |
rs148149501 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43393370 | TTTCACAGTCAATAA[A/T]CTGTAAAGAGTCTGT | 23072 |
rs148154753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298166 | GGAATAGAGTGCACC[A/G]TTCGCCCTGTCTGGA | 23072 |
rs148170855 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519577 | GCTATGCTGGACTGC[C/T]GCACAAAACACCCAG | 23072 |
rs148181476 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43534083 | TCAGACTTGGCATAT[C/T]GCCTGGGTGCTGCAC | 23072 |
rs148183529 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139133 | TTATTCTTAATGAGC[A/G]GCTCTGATGTGAATG | 23072 |
rs148186086 | in-del | -/T | 0.25634 | 0.24992 | intron-variant | HECW1 | GRCh38.p7 | 7:43258286 | AGGCGGAGGTTGCAG[-/T]GAGCCGAGATTGTAC | 23072 |
rs148187116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351919 | TGTATTTCTCAACAG[C/T]ATATCCGTTTATTAT | 23072 |
rs148191058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428636 | GTTTGACCAAGGTTG[A/T]CCAAGATATACAGAT | 23072 |
rs148200862 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43471216 | CATTGATAAGGGGAA[C/T]AGATTGAGAAAAGTA | 23072 |
rs148230610 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145184 | TGAGATATGGGTTGA[C/T]TGGATTGTGGGTTAA | 23072 |
rs148265202 | in-del | -/T | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43321784 | TTCATTTTCATTCAC[-/T]CTTATTTTCATTCAC | 23072 |
rs148267539 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124984 | ACCATAGACTGAGTG[A/G]CTTATAAACAACAGA | 23072 |
rs148277827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43491035 | TGGGATTACAGGTGT[C/G]AGCCACCGCACTGGC | 23072 |
rs148278095 | snp | A/C | 0.433236 | 0.170072 | intron-variant | HECW1 | GRCh38.p7 | 7:43416707 | GTAGGACCCTCCGAG[A/C]CAGGTGTGGGATATA | 23072 |
rs148286854 | in-del | -/AC | 0.0399052 | 0.1355 | intron-variant | HECW1 | GRCh38.p7 | 7:43175187 | TGTACACATACACAT[-/AC]ACACACACACACGCA | 23072 |
rs148304761 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156501 | AAATTAATATTTCAG[C/T]GATAACACAACTGCA | 23072 |
rs148305770 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43443001 | TTCTACCTAGTAACT[A/G]GATATAGACTAGCCA | 23072 |
rs148315688 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43366248 | TCAATAGGACATTTC[A/C]ACACCAATATAGGCT | 23072 |
rs148321154 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43564148 | AATCAGAGCATAAGG[A/G]CTATGCAAATCATTG | 23072 |
rs148321563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43191079 | GAATCCCACAGTTTA[C/T]TAAATCAATATAAAA | 23072 |
rs148328237 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43486452 | GGCTACAGGCACGCA[A/C]CCCTACACCCGGCTA | 23072 |
rs148336316 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HECW1 | GRCh38.p7 | 7:43309171 | GAGCAGAAAGTTCCA[C/T]TCTTGGGAATGGGAA | 23072 |
rs148345569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43325852 | CCCAGATTGCTGCAC[A/G]CTGTGGTCTCATCAT | 23072 |
rs148349704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389062 | AGATGCAGGCCCAAG[A/C]CCTGAAAACAAAAGC | 23072 |
rs148351926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43218475 | TTGGGTCCTGATAAC[A/G]CATTTTGGTGGAGAA | 23072 |
rs148360016 | snp | A/G/T | 0.013097 | 0.0799021 | intron-variant | HECW1 | GRCh38.p7 | 7:43436901 | ATGGAGTCTCACTCT[A/G/T]TCACCCAGGCTGGAG | 23072 |
rs148361547 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43547712 | ATTTTGAAAAGATGG[A/G]CAACCACATCTGCAG | 23072 |
rs148362253 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514289 | TTCCAAATTTCTTTT[C/T]TCTTTTCTTTTCTTT | 23072 |
rs148365991 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43260403 | AAAGTGGCAAGATAG[A/G]TGCAACACAGGGAGC | 23072 |
rs148372257 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43559913 | AGTAAACCATGAGTG[A/T]TCAGACTAGGTGCTA | 23072 |
rs148385105 | in-del | -/TC | 0.0558544 | 0.157504 | intron-variant | HECW1 | GRCh38.p7 | 7:43335858 | CCCTTTCTCCCTTCA[-/TC]TCTCTCTTTCTCTTT | 23072 |
rs148399178 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43375296 | TGTCTATTTAAAGGG[-/A]AAAAAAAAATAGTTC | 23072 |
rs148402703 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544595 | CTTTGACTCAGCACA[-/AT]CGTCTAGAAATTTGT | 23072 |
rs148410875 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43368140 | AAACAAGACAAATCC[C/T]CATGCTCATCAAGCC | 23072 |
rs148421487 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43266822 | ATTTAAAAGAGACAC[A/G]CAAAAGGAATGATTA | 23072 |
rs148421708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43193908 | ATTGTGAATGCCCCC[C/T]ACAAGAGACAGCTTT | 23072 |
rs148425291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43487503 | GCAGGCCACCAAGGG[C/T]TCTCTCTCCCCTCGC | 23072 |
rs148431570 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43310799 | CTGGGATCTAAACTT[C/T]ATGAGTCAACACTTT | 23072 |
rs148435310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43378122 | ATGTGTGTTACACTT[C/T]CAGATTTGAAAAAAA | 23072 |
rs148436020 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43205146 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 23072 |
rs148445443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43391499 | CAGTTAAAATAGTGC[A/G]TATGGAAGAACTGGC | 23072 |
rs148452681 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43220278 | CACCTAGAATGCAAC[A/G]CTTCCTGTGTCCTCT | 23072 |
rs148454144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328473 | GTCCCTGTCTGAACT[G/T]CATGGGGCTGCCAGA | 23072 |
rs148456567 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153185 | TTTTTTAAAACCACT[C/G]ATCTCCATCAAGCCC | 23072 |
rs148461961 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122060 | ACTCCACAAGGACAG[A/T]TTTTTATTTGTTTGT | 23072 |
rs148466932 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516976 | AAATGGTACACCTGT[A/G]TAGGGCAGCTCCGTT | 23072 |
rs148467070 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43439072 | CCAAAGGGAGCTGAG[C/T]TTATGGAGCTGCAGT | 23072 |
rs148476564 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43561088 | CTTCTTGTACCCACT[A/G]CTGGAGAGCCACATG | 23072 |
rs148482189 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43373287 | TGATCTGGGCTCACT[A/G]CAACCTCTGCCTCTT | 23072 |
rs148495100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43468007 | CACATGGCCATGCCC[C/T]AGCCCTGGGTGCAGG | 23072 |
rs148502989 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43289989 | GAGTTAGGATAAAGC[A/C/G]GGTTGTGGAGGCCAA | 23072 |
rs148505442 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43386757 | GCTCAGATGAGGGAG[A/G]AATGTGTCCATCAGT | 23072 |
rs148511017 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215642 | CTTTATGCATTTCAT[A/G]ATTTATCAAGGTTTT | 23072 |
rs148538297 | in-del | -/GTGTACAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43439150 | TTAAACAGACAAAAA[-/GTGTACAT]AAAGAACCTAGCACG | 23072 |
rs148549523 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43462125 | TGCAGCGAGCATCCC[C/T]GTGCTTTCCCACCTG | 23072 |
rs148551048 | in-del | -/GTGTGTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361058 | TGTTCTTGTGCGTGC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 23072 |
rs148554071 | in-del | -/T | 0.160609 | 0.233472 | intron-variant | HECW1 | GRCh38.p7 | 7:43503701 | ATTCTCTTAGACTGG[-/T]TATGAAATCTACCCA | 23072 |
rs148586263 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43351092 | GTCCCCTTTTCCTAC[A/G]GTGTGGCTTCCTGTG | 23072 |
rs148588096 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | HECW1 | GRCh38.p7 | 7:43278479 | CCCACCCATGCGGCC[C/T]GTTCTCATCACAGAC | 23072 |
rs148598595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43179171 | TTGCTTTCCGCAGAA[A/G]ATAATAAATGCAAAA | 23072 |
rs148608740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189644 | TGAAAAATAAATACA[C/T]GGGGTTAAAAGTAAA | 23072 |
rs148612979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119208 | CAGGTATCAGTCACT[C/T]GTTCCTGTCACTCCC | 23072 |
rs148614859 | in-del | -/CCCCTCCCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316786 | CTCCTCCCCTCCCCT[-/CCCCTCCCC]CCTCTCCTCTCCTCT | 23072 |
rs148624381 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43404016 | AAATTCTAGAACTCT[A/G]TGTGCTCTTATGGAC | 23072 |
rs148624920 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43231019 | GTCTGTTCTGTAGGG[A/G]ATAGATGCTATGTGT | 23072 |
rs148629206 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43306848 | ATTTTCTGCTTTTAA[G/T]ATTCTGTTTTTTTAC | 23072 |
rs148632528 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HECW1 | GRCh38.p7 | 7:43526616 | TCTGCCCGGAACACA[A/G]TGGCATTGCCATTCC | 23072 |
rs148633194 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129806 | CAAGTCGCTGGTATA[C/T]GATGGTGTGGTACCT | 23072 |
rs148639481 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43347806 | TTTCAATTCTGTTTA[C/T]GTGGTATATCACATT | 23072 |
rs148644087 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43421019 | AGAAAAAAAAAGCAG[G/T]ACTTTTATACTGCCG | 23072 |
rs148650270 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43175017 | TCAAGGATTAGAACA[G/T]CTCGAGGTACCTATG | 23072 |
rs148659513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43259171 | GAGGGGGGATCACCT[A/G]AGGTTAGGACTTCGA | 23072 |
rs148661238 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43360683 | GGATACAAAAATGTT[A/G]AGGCCAGAACAATTT | 23072 |
rs148667052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184983 | AGGGAGCATGGTGTT[G/T]AACCATTAGAACCAC | 23072 |
rs148671210 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43396390 | ATAATAATAAGTGGA[G/T]ATGCAGCAGTTCAAC | 23072 |
rs148673833 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43369626 | CCTAGAAATTGTGAA[C/T]GAACACATCAAGATA | 23072 |
rs148674815 | snp | G/T | 0.000315922 | 0.0125643 | intron-variant | HECW1 | GRCh38.p7 | 7:43479780 | CCCTACTGTTCACCG[G/T]TCACAGTCTCTGCCT | 23072 |
rs148682715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299945 | TCACCTGATTTGCTG[A/G]TTTTGATCACAGGGA | 23072 |
rs148684467 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521467 | GTATTTCTGTAGGCC[C/T]AGAGTTTTAGGAAAA | 23072 |
rs148692173 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43539998 | AGTGCCCCATAGCAC[C/T]TTCACTGAGGTTTTG | 23072 |
rs148698351 | in-del | -/ACA | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43243347 | CAGTCACTCCGCAGG[-/ACA]ACAAGTGGAAGGGGA | 23072 |
rs148708089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43535600 | CATCAGAGGGGAAAC[A/G]GCTGAACCAAGCATA | 23072 |
rs148710863 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | HECW1 | GRCh38.p7 | 7:43331034 | GTACATGTGCACAAC[A/G]TGCAGGTTTGTTACA | 23072 |
rs148713148 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43254915 | TCACCCCCACTAGGG[A/G]CTGCCATCTTGGTTT | 23072 |
rs148714919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43355645 | CTACCAGAGAAAATA[A/G]CTTAACCACAAAGGA | 23072 |
rs148730123 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43473564 | AAATATGGGAAAAGT[A/T]GTATAATACAAATGG | 23072 |
rs148732222 | snp | C/T | 3.3145e-05 | 0.0040708 | HECW1 | 7 | allele_origin=T(somatic)/C(germline) | 7:43444313 | GGCAGTGGGGAACCT[C/T]GGTCTGAGGCACCAG | 23072 |
rs148758283 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43500488 | TGCTGTGTTCCTCAG[C/T]TTCTGTACCTGTGCA | 23072 |
rs148759419 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43425482 | TCTCTTGTTTCTTGC[C/T]CCAGCCTCCTGCGCT | 23072 |
rs148790706 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43492849 | GTAAAGATCCTGAAA[C/T]GTTAAGGACGATTAA | 23072 |
rs148798927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43315835 | GTCCAGCCACAGTGG[A/G]AGAATCCTGGGAGAT | 23072 |
rs148804943 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43210841 | GTAGTGGGTCTGCAA[A/T]GGCGGTAAATATCAA | 23072 |
rs148807006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43240902 | GGTCTGCAGAGGGAC[C/T]CTCCCCACGTGACTT | 23072 |
rs148809512 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140784 | CTCAGTTCTGGAGGC[G/T]GGAAGTCTGAGGTCA | 23072 |
rs148812135 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43411046 | CTTTATTGCCTTCTA[-/T]TTTTTTTTTTTTAGC | 23072 |
rs148814993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509840 | GGAAATGAGTCCTGG[A/C]GATGGCTAATGTGAG | 23072 |
rs148821787 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43332868 | TTATGGAACCCTAGA[G/T]GGCAGATATTTTTAT | 23072 |
rs148824771 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43555109 | GGGCAGAGGCAAGGA[A/C]ATTAATATAAAAATG | 23072 |
rs148859333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150939 | CAGGCTTCACTTGGC[A/G]TGGACAACTTGCTAA | 23072 |
rs148866951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43503064 | AAGTCCCTCTTAGAG[A/G]TAGTTGTGCTCGTCG | 23072 |
rs148899082 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43383444 | GCCTCGCCAGCATCT[A/G]TTGTTTCCTGACTTT | 23072 |
rs148906332 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213030 | TTATATCAGTAAAAG[C/T]GTAATGAAATTAGTA | 23072 |
rs148907932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43318850 | GTTGTCCCTCCAGCC[C/T]CTACGGTGGATTTGG | 23072 |
rs148911095 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143217 | CTCAGATGATCCACC[C/T]ACCTCAGCCTCCCAA | 23072 |
rs148912395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43538558 | CCAGAACCCAGAGTA[A/G]CAACCTCTCCATCGC | 23072 |
rs148948346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43173229 | ATGGTGACTAAAAAA[A/G]ACGCAGAGGAAAATT | 23072 |
rs148949025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43460535 | GTACGTGTGTGTGCG[C/T]GCGTGCGTGTGTGTG | 23072 |
rs148953705 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43490385 | CCCATTCTCACACCA[C/T]TCTTTGATCAATTAA | 23072 |
rs148956545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43282407 | GGCGACAAGGGTCAG[A/T]TCTGCCTTCTGTAAA | 23072 |
rs148958563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43379976 | CTGGCACACAGCAGA[C/T]GGCCCATAAAACATT | 23072 |
rs148968958 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43393269 | AGGGAGCTTGTCAGC[C/T]CTGAGAAGACCAGCC | 23072 |
rs148975556 | in-del | -/C | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111281 | TGCTGTTGCTGTTTA[-/C]CTGCCACAGCCTGTT | 23072 |
rs148978834 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297669 | ACTGAAAAATACAGC[C/T]GCATTGGGTTTGGCT | 23072 |
rs148980746 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | HECW1 | GRCh38.p7 | 7:43221806 | TGCTTTGGCCTCCCA[A/T]AGTGCTGGGATTACA | 23072 |
rs148983047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123428 | CCGAGAGACCACTGC[C/T]GTAGGAACATGCTCT | 23072 |
rs148988408 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43342460 | TTGATTATTTCTCTA[A/G]AAGTACTGCTCTTAT | 23072 |
rs148991837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43442212 | TGATTTTGCATACTT[G/T]TAGGCTAATGTAAGT | 23072 |
rs148993860 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43411586 | AAGAAGCATGTTTAA[A/G]TCCTTTACTATGTTC | 23072 |
rs148999644 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43167044 | CCCTTTCTGATGAGA[C/T]AGTGGATTCACTTCC | 23072 |
rs149004370 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563634 | AGCACTTTGGGAGGC[C/T]GAGGTGGGGAGATCG | 23072 |
rs149021490 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | HECW1 | GRCh38.p7 | 7:43388018 | GAACTCAGTGAGATA[C/T]GTTTTATTATGATCT | 23072 |
rs149026040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43470693 | GAATTTCAAATGAGA[A/G]GACTTTCAGTTATGA | 23072 |
rs149031728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43291295 | CTTACTGCTGTGTCT[C/T]GCATCCATTGGCTGG | 23072 |
rs149036260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513194 | TGTGCAATTAATTGC[C/T]CAAATTTCACACTTT | 23072 |
rs149077152 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43545181 | AGAGATGACTGTCTC[C/T]AGAAAGGGAGATTGC | 23072 |
rs149077770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43463996 | CCCACCAGGAAACTT[A/G]GGAGAAGTGATCACA | 23072 |
rs149113857 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43252961 | AGTGGCCAACCTTGG[G/T]TAGAGTTCAACTTTG | 23072 |
rs149116540 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43351636 | ATATCTGGAAATTCT[A/G]TGTATCTGCCTTTTC | 23072 |
rs149118356 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43279719 | ACCTTGATTCTCTTA[C/T]GGCACCTGATTTTTT | 23072 |
rs149137660 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43190537 | AATACATTGATACAG[G/T]GGAGCCATGGATTGA | 23072 |
rs149139100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43485858 | CACTTAGGCTACACT[A/G]AATTTTTTTTATTAT | 23072 |
rs149146372 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43309037 | CATGGCAGGAATTAT[A/G]CCAGGTACAGGGGAT | 23072 |
rs149154335 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43232277 | CTCCACTGGTGAACT[A/C]TAAGAACCCTCCTTC | 23072 |
rs149156116 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131037 | TTGGGAGGCCAAGGC[A/G]GGTGAATCACTGGAG | 23072 |
rs149160006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43423420 | TGGGAGACTGGAGGT[A/C]CTGCCTCTTGTTCTA | 23072 |
rs149161588 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43528249 | AGCTAAGGAGAAATC[A/T]TGCTTTAGAGGTCAA | 23072 |
rs149168682 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43246225 | GGAGAATCGCTTGAG[C/T]CCAGGAGTTCCAGGC | 23072 |
rs149179736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43362387 | TCCCGGAACTCATAG[C/T]GGGAAGCGCAGTGGG | 23072 |
rs149184549 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43436838 | GTCACACCATACACT[A/G]TTTAACAAACAAGTA | 23072 |
rs149190710 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43260225 | AGGACAGATAATAGA[C/G]GGTACAATCTGGTTA | 23072 |
rs149194810 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43480995 | CCAGTGTGATAAAAT[G/T]AATGTTTTTTCATGG | 23072 |
rs149196819 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43559710 | GCCCCACACCACCGG[A/G]CAATGCTTGGTTTGG | 23072 |
rs149200592 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302703 | TGGAGCTGGGCGCCT[C/T]GGGCCCCTGGAGCCG | 23072 |
rs149222722 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43418246 | AGACCCTATTTCCAA[A/G]TAAGTTTGCATTCAA | 23072 |
rs149234360 | in-del | -/AAAGAAAACA | 0.0879971 | 0.190408 | intron-variant | HECW1 | GRCh38.p7 | 7:43499492 | AAGAAAGAAAGAAAG[-/AAAGAAAACA]AAAGAAAAGAAAATC | 23072 |
rs149253026 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140194 | TGGCTCTGTTTCATC[C/T]ATATTTCTCCTCATT | 23072 |
rs149256913 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43310097 | TTCATAATTATTTTG[A/T]ATCTCTGTAATACTG | 23072 |
rs149258359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135519 | CTCTGGACTTCTTGC[C/T]ACATAAGAGAAAATA | 23072 |
rs149260738 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | HECW1 | GRCh38.p7 | 7:43530053 | CTCCCAGGTTCAAGC[A/G]ATTCTCCCACCTCAG | 23072 |
rs149261039 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43205126 | TCTCGCACTATTGCC[C/T]GGGCTGGAGTGCAGT | 23072 |
rs149266624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43349805 | AGTTATCCATTCTGC[C/G]GTTCTGTATCTTTTA | 23072 |
rs149277749 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43249785 | GCCACAGATGCCTCT[C/T]TTGCTTGGTAGTGCT | 23072 |
rs149287555 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43262414 | GTATTGATGATATTA[C/T]TTCACATATGATGAA | 23072 |
rs149292043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43188957 | ACATTTAAGCCAATC[C/T]GTGGATTCCTAGAAG | 23072 |
rs149296295 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43164908 | AGCTCATTCATCAGC[C/G]AGTGTCTTAAGAGTG | 23072 |
rs149302149 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43560957 | TCCACCTTTCTCTCT[A/G]CTACGGTACAGGACT | 23072 |
rs149303460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43482742 | AGGACCTTTTCTCTA[C/T]AAAAATTTAAAAATT | 23072 |
rs149306216 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43275621 | CACCTCCCCAAATTA[C/T]GGAGCTGCCTTGAAG | 23072 |
rs149310501 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | HECW1 | GRCh38.p7 | 7:43306002 | CAACCTCAGATGATC[C/T]GCCCACCTCAGCCTC | 23072 |
rs149312967 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43200001 | GAATGGAAGAAGTCA[C/G]TAAGCGTCGCTCAAT | 23072 |
rs149318980 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43419940 | TCACATTCTGTATTT[G/T]TCCCGATTGGCTAGC | 23072 |
rs149323452 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43495317 | GCTCCCTGTGTCCAT[A/G]TGTTCTCGTTGTTCA | 23072 |
rs149338454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43334656 | ACAAAAAGCAGAAAA[G/T]AAAAAGGAGAAAGTC | 23072 |
rs149347812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257976 | TTCCCAATCCTATGA[A/G]TCTGATATTGTCTTC | 23072 |
rs149354193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43556067 | TCTAGGGAGAACACG[A/G]CCTGATAGTAACTAA | 23072 |
rs149361544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43369038 | GCCCTGGTGTTTCAT[A/G]GGCACATTTGCACAT | 23072 |
rs149392758 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43330291 | AAGCCCTGGCTAGCT[A/G]TGTTCGGGGCTGTGT | 23072 |
rs149409639 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43537549 | CCATTACTAGAAGGT[G/T]TTTTCTCATTCATGG | 23072 |
rs149424703 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43385346 | TTTGTGTCAGTGTCA[C/T]TCAGACACTGTTGCA | 23072 |
rs149434393 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147122 | GTTATCCAAGGAAAC[A/C/T]TTTACTAGGCTTTCA | 23072 |
rs149437083 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43215336 | AATCCTCACAGAAGC[A/G]TTGCCCTGTCCTAAC | 23072 |
rs149437798 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511482 | CTTCACCTCCACGGG[A/G]TCAGAGATCAGATTG | 23072 |
rs149438625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117743 | ATGTGTGGGTATTGG[C/T]AAGTAGTTGTACTGT | 23072 |
rs149464310 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | HECW1 | GRCh38.p7 | 7:43271851 | TTGGAAAAAACTATG[C/T]TAAAATTCATATGGA | 23072 |
rs149472648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43174407 | TTAGTTTCTGCAGCT[A/G]TTCTACTCCTTGATC | 23072 |
rs149483808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43461939 | CTTCCTAAAGAACTC[A/G]TTAGAAATGCAGATT | 23072 |
rs149489146 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43209686 | GCGAAGCCTGGAGTA[G/T]CAATGTCTTTCCACA | 23072 |
rs149498793 | snp | C/T | 0.021333 | 0.101051 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299344 | TGTATATTTGGTGCA[C/T]CTTTGGTGTATCAGA | 23072 |
rs149508301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124552 | ACAGAACTTATATTT[A/G]TTAAACCTGAAAGAG | 23072 |
rs149516388 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521032 | AGGTTTCATGCCTGC[C/T]CCAACTCTCAGTAGA | 23072 |
rs149520236 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43238834 | GTCATAGAGGAGGGG[A/C]CTGGGAATTTGGAAG | 23072 |
rs149522434 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | HECW1 | GRCh38.p7 | 7:43343812 | TGGTATTTCTAGTTC[C/T]AGATCCTTGAGGAAT | 23072 |
rs149524932 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43169339 | GGCTGACCTGCGCAT[C/G]GCAGGGTGTGACACA | 23072 |
rs149534421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43533985 | GAAGGTCACCCAAAG[A/C]AGGAGACCCCTTGAA | 23072 |
rs149535584 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43459103 | ACCTGCCTCCCACCT[A/G]AAACATATCTCATCC | 23072 |
rs149550215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43365292 | ATGAGACCCTCCCTA[C/T]AGAGCGTTCACCTGG | 23072 |
rs149559912 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120583 | TTCCTTAACTGAAAT[C/T]CAACCTCAGAACTTT | 23072 |
rs149567932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515060 | GTGCTTATCACATTG[C/T]ATTGTAATAATGAGG | 23072 |
rs149572751 | snp | A/C/T | 0.0532157 | 0.154195 | intron-variant | HECW1 | GRCh38.p7 | 7:43406692 | GGAGGCCGAGGCGGG[A/C/T]GGATCACCTGAGGTC | 23072 |
rs149576819 | in-del | -/ACTC | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43257049 | TGATTGTTATTAGAT[-/ACTC]ACTCATCCTTTTCAT | 23072 |
rs149593914 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43184864 | AAGGTGAAGGGGAAG[C/T]AGGCAGGTCTTACAT | 23072 |
rs149605998 | snp | A/C | 0.00157242 | 0.0279953 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43466538 | GTTCATCACCAACCC[A/C]GAGTTCTTCACTGTG | 23072 |
rs149608230 | in-del | -/AC | 0.0236746 | 0.106192 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297244 | TGAACTGAATTAGAT[-/AC]AGTCAGAGCAAGGGC | 23072 |
rs149628645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140679 | ATTAGGAGAACCCAA[A/C]GTAATGCAAATGCTC | 23072 |
rs149635163 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43354935 | ATAAAAGCAAAGAAC[A/T]TATAAAGGAACTCCA | 23072 |
rs149646364 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | HECW1 | GRCh38.p7 | 7:43254588 | ACAATCTGCTGACAC[C/T]ATACTAGCAGGAACC | 23072 |
rs149648871 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43472706 | AAGGTAATTAAAATA[C/T]ATTATATATCTACAC | 23072 |
rs149653865 | snp | C/T | | | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295774 | AAGCAATAATTCCTA[C/T]ATCACTTTGGTAAGG | 23072 |
rs149658306 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43367415 | TTTAACTGAAGTAAT[C/T]CTAGTTATGCTAGGG | 23072 |
rs149667253 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43303938 | AGAGGGAGAGGAGGA[-/C]CCAGGGGCAGTATTT | 23072 |
rs149667974 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43409824 | CCCCTAAATTGTACT[A/G]CAGTTCCCAGGGTCC | 23072 |
rs149711778 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43363719 | TAGGAGCCACTGGGA[C/G]GAGCCCCCTTTGTTT | 23072 |
rs149727102 | in-del | -/GAA | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43446027 | ATGTTAATATTAGTT[-/GAA]GAACAGATTTTACCT | 23072 |
rs149734686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43431839 | GGCACCCCTCTACCT[A/G]GAATGTTCCTCCCAC | 23072 |
rs149746628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43183084 | ATATTTTTGAGCATC[A/T]CCTAAGCGCAGTGCT | 23072 |
rs149756051 | snp | A/G | 9.34689e-05 | 0.00683562 | intron-variant | HECW1 | GRCh38.p7 | 7:43554814 | CTCCTGCCAGCCTTC[A/G]GGGAAACCTGCTGAA | 23072 |
rs149757595 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43475307 | AACTGAATTGTAAGT[A/G]AATTTAAGCACAATT | 23072 |
rs149771946 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43379568 | CCATCATTCCTGCTG[C/T]TCTGCCCTTGCCTGA | 23072 |
rs149775043 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43312702 | AAACAAAACAAATTA[G/T]GCAAATAAGTTGGAT | 23072 |
rs149779652 | in-del | -/TCTT | 0.0418186 | 0.138422 | intron-variant | HECW1 | GRCh38.p7 | 7:43335752 | CTTCCTCCTTTCCTC[-/TCTT]TCTTTCTTTCTTTTT | 23072 |
rs149784189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206526 | TCTACTTCAATTCTT[C/T]AGTGGTTAACTTTCA | 23072 |
rs149788125 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43502812 | TTGTAGGTTTCATTT[A/G]AAGTAAAAGAGATCA | 23072 |
rs149796721 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43427158 | TCTAGGTTGACAGTT[A/G]TTTTTCCCTCAGTAC | 23072 |
rs149802672 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | HECW1 | GRCh38.p7 | 7:43251969 | GGGGGGGTACATTCC[A/G]CGGGGTCCTTGGCTT | 23072 |
rs149803345 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152807 | TGTAGGCGTTTCCCC[C/G]TGAGCTGGTTGTTTT | 23072 |
rs149807320 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43438805 | CTTTAGGTAACAGGG[A/C]CTACATTTGAAAACA | 23072 |
rs149811693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43548897 | TGCAGAGAGCTGAGA[C/T]TGTACCACTGCACTC | 23072 |
rs149812206 | snp | C/G/T | 0.0337553 | 0.125452 | intron-variant | HECW1 | GRCh38.p7 | 7:43264579 | AGCCAGGCGCGGTGG[C/G/T]TCACGCCTGTAATCT | 23072 |
rs149816170 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43342239 | AGTGGAATCATCAAT[A/G]TTAGATGCCTCGTCA | 23072 |
rs149818761 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562679 | AGGGGGAGCATCCCT[A/G]GTGAATACTCACACC | 23072 |
rs149820517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43166925 | GCATGTGGATGACCC[C/T]GTGTGCCAGGCCCCA | 23072 |
rs149825959 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375531 | ATTACTTAAATATAT[A/G]TTGTATGGCTTATTG | 23072 |
rs149831540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43455858 | ATACCAAAATTAGCC[A/G]GACCTGGTGGCAGGC | 23072 |
rs149836466 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43201574 | CTTTACATTCCCCGT[G/T]GTAGATTTGTGACTT | 23072 |
rs149837646 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43278179 | TGGGATGTCTTATAA[A/G]CATCTCAAACTTAAA | 23072 |
rs149840474 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43497580 | GTGGGGAAAAGATAG[A/G]CTGGGGAGGGGCATA | 23072 |
rs149847829 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43321255 | ATTGGTACTACCAGC[A/C]TGTTTCTTTGATTTT | 23072 |
rs149872967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162050 | AAAAAATGATTTCAC[A/G]TTAATGAACACCATA | 23072 |
rs149874347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43559191 | CTGTGTAGATGACAC[A/T]GTTAGAAGGATAAAC | 23072 |
rs149874737 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43229774 | AGTGTCTCTCCACAA[A/G]ATACTCATTATTTAC | 23072 |
rs149883988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43450198 | TCTGATTTCTCCTCA[A/G]AATAATCTGGACAGT | 23072 |
rs149921213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43395679 | GCTTCAGGGCAGTCA[C/T]ACCAAGATTTGTCTA | 23072 |
rs149953387 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43290978 | TGCATATGGAGAATA[C/T]TCACAGTGGTAACAT | 23072 |
rs149959302 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43216808 | TACAGGCACCCACCA[C/T]CATGCTCGGCTAATT | 23072 |
rs149962121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118897 | GACATTTATAAAACC[A/G]CTCCCTGACTCCACA | 23072 |
rs149964291 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | HECW1 | GRCh38.p7 | 7:43435947 | AGGCAGGCGGATCAC[A/G]AGGTCAGGAGATGGA | 23072 |
rs149966352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43403494 | GATCCCCCTGGTAGA[C/G]AGCGGAAGAGGGACA | 23072 |
rs149977884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130429 | TGTGTACATTGAACC[A/G]TCAGAAAGCAAGGGT | 23072 |
rs149994835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43176076 | TACTTGAGGAGGAAA[A/G]ATGGATTTCCTGATA | 23072 |
rs149998371 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43463873 | GCTACAAGCCTCCCA[C/T]CCTGCCTCATGGGGA | 23072 |
rs150006065 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43285598 | GTGGATTGCTTGAGC[A/C]TAGGAGTTTGAGACC | 23072 |
rs150008481 | snp | A/C | 0.00677148 | 0.0577918 | intron-variant | HECW1 | GRCh38.p7 | 7:43383116 | GGACATGAACTCATT[A/C]TTTTTTTATGGCAGC | 23072 |
rs150013554 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112402 | CGAGGAGCCAGGGTT[A/G]GTGTTGGATATGCCC | 23072 |
rs150021905 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508782 | GAAACATCTCCAAAC[C/G]AATTACTGCATCCTC | 23072 |
rs150027797 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43226306 | TAATTTTGCTCATAT[C/T]CTTTAAACAACCTGA | 23072 |
rs150028867 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302155 | AGGCAAATGAGGACA[C/T]GACCATGAATGGAGG | 23072 |
rs150029573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126115 | CACCACTGTACTGAC[A/G]AGGATCACTTTCCTA | 23072 |
rs150032041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522337 | GTCTCGGTGCAGTTA[A/G]TCCACTGAGTTCATG | 23072 |
rs150036971 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43417760 | TCCAATAATAAATCT[A/G]TAATGATTTAAATCA | 23072 |
rs150038801 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | HECW1 | GRCh38.p7 | 7:43346201 | TTCTTGCAGGAGTAA[A/G]GTGGTATCACATTGT | 23072 |
rs150048298 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43240222 | GGGCGCTTGTAGTCC[C/T]AGCTACTCGGGAGGC | 23072 |
rs150048874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43535311 | AAATGTGCAAAACCC[A/G]GATGGAACTATGAGA | 23072 |
rs150059404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43460099 | CTGTTTTTTGTCACA[A/G]GGGCCTGCTAAATAC | 23072 |
rs150077962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135343 | TCTTACTCTTCCTCT[C/G]TTAGATCTGGAATGT | 23072 |
rs150095102 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | HECW1 | GRCh38.p7 | 7:43178653 | CTTGTCTTGCGTTCT[C/T]TCACATCCCTAATTT | 23072 |
rs150097458 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43249648 | ACTGCATAGCTATTT[C/T]CTTCAGGCAGCATGT | 23072 |
rs150108307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286875 | GGGTCATCATTTAAG[C/T]TGTCCATACTAATGA | 23072 |
rs150111849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43362065 | AGAATCACTTGAACC[A/C]AGGTGCAGTGAGCAG | 23072 |
rs150116237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43185792 | CATTAGGATAGAATG[A/C]GTTTTGAGTATTTGT | 23072 |
rs150120431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116636 | TCTCTCCCATTTACC[C/T]GCTTCCTTTTCCATC | 23072 |
rs150127012 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43480933 | GAGTCCTGTGTATAC[C/T]CTGAGAAACATAACT | 23072 |
rs150133007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43199801 | GTGTTCCAGTACCCA[C/T]GAATGAGTGCTATTT | 23072 |
rs150142770 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43318524 | GGGGCAGCCTAAAAT[C/G]TGCAATCCACATAGC | 23072 |
rs150144065 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | HECW1 | GRCh38.p7 | 7:43419739 | TTGTTTCCCAATGCC[A/G]TAAAGAAATAGCATT | 23072 |
rs150149208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242682 | GAGGCAGGGACATGG[C/T]CCTAGTGTGTTCCTT | 23072 |
rs150151081 | in-del | -/TATT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43489360 | CAGAAAGCCTTTACA[-/TATT]TATTTATTTATTTAT | 23072 |
rs150153827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43461212 | CAGTCAGAGGGTGGC[C/T]GGGGCTGGAGACTCA | 23072 |
rs150160224 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43537966 | GTCGCCACACCCCCT[C/G]GTTGAGAGGCATGCA | 23072 |
rs150165381 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43357741 | TTTATAATATGTTTC[C/T]AAATGGCTACAATAA | 23072 |
rs150181700 | in-del | -/AAT | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43476206 | AAAAGTAAATACACA[-/AAT]AATAACTTTCCTGAG | 23072 |
rs150183994 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298291 | ATTAAATTTTCACGC[A/G]AATAAGTCCTAAATC | 23072 |
rs150186263 | snp | A/C | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269515 | CACATGTGAAATTCA[A/C]ACTTGAAGCATATTT | 23072 |
rs150188335 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43489421 | ATTCAATACTGCATA[C/G]TTTATTGATCAGCAA | 23072 |
rs150196497 | in-del | -/TTATTATTA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315466 | GTCCCATTATTATTG[-/TTATTATTA]TTATTATTATTATTA | 23072 |
rs150211785 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43533260 | GCAAAAGACTCCTTA[A/G]AGGAACTTAACCCAT | 23072 |
rs150265387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257833 | GTCTTAATTTATTCA[C/T]ATGCAATTAGAAATA | 23072 |
rs150271233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43555995 | ATCACTGATGATAGC[A/C]TGCAGCTTGAGGAGG | 23072 |
rs150279988 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43368794 | TGCCATAGTGTAGGG[A/G]TGGGTGGTTTACATC | 23072 |
rs150282119 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43477299 | TTTTTCTAACTTTAA[C/G]CAAGTAATTAATTCA | 23072 |
rs150305486 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43209550 | TCCTGTCTCAAAGAG[A/G]TTAGAATTTGCAAGA | 23072 |
rs150310306 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139636 | TTTTATTATAATACC[G/T]TCTTAATTTTTCTGC | 23072 |
rs150310835 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43428736 | CTTTTCTTCCTTCTG[C/T]GTTCTGGGCACTCTA | 23072 |
rs150316467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43505580 | TGTTTTTGTACCACT[C/T]TGGTCCTTGGACTCT | 23072 |
rs150318572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253630 | ATATCATCAACTTTG[A/G]CATTCCCTCCAATGT | 23072 |
rs150323097 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43330016 | AGGACGGAATTCCAT[C/G/T]GAGGAGCAAGAGGAA | 23072 |
rs150323740 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155152 | TCAAAATAACAAACT[C/T]TGTGCTTTGCTCTAC | 23072 |
rs150326219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550747 | GAGTGCTCCTCACCA[A/G]GGAGTACTGAGGATC | 23072 |
rs150326388 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | HECW1 | GRCh38.p7 | 7:43221679 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 23072 |
rs150327140 | in-del | -/TTAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224666 | TCTACAGAAAATAAA[-/TTAG]AAGCCGGCCATGGTG | 23072 |
rs150345556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43458377 | ATGAAAGTTTATCGG[A/G]GTGATCTGCTTGCAT | 23072 |
rs150353276 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514317 | TTTTTTTTTTTTTTG[A/G]GATGGAATTTCGCTC | 23072 |
rs150355249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376731 | ATTAGCTGGGCGTGG[A/T]GGCAGGCGTCTGTAA | 23072 |
rs150361056 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43345178 | GTTATGAATATTCAC[-/A]AAGGGGTTCCTGAAA | 23072 |
rs150368327 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43499364 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCACAAG | 23072 |
rs150370085 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43323896 | AAAATTAGCCAGGCA[C/T]GGTGGCATGAGCCTG | 23072 |
rs150374393 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43387777 | GCCCCGATTTGTCTG[C/G]TGTGACCAGTTATGT | 23072 |
rs150393419 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43164387 | CAGTGTTTTGCATAA[A/G/T]TTGAGTTGAAGGTGC | 23072 |
rs150399128 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43528161 | TTGCGACTTGTAGAC[A/C]TAATCTCAGTCATGA | 23072 |
rs150407648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43452449 | CAGTTTTCTATCCAT[A/G]TAACAGTGAAAGACC | 23072 |
rs150413563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43274537 | GCAGCCAACAAGTGC[C/T]GCCGGGCCACGCTTC | 23072 |
rs150437603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43343406 | GTATTTCTCCTAATG[C/T]TATCCCTCACCCTGC | 23072 |
rs150459406 | in-del | -/TA/TTATTATTATTATTA/TTATTATTATTATTATTATTA | 0.466308 | 0.125343 | intron-variant | HECW1 | GRCh38.p7 | 7:43430779 | CATTTTTATTTTTCT[lengthTooLong]TTATTATTATTATTA | 23072 |
rs150480928 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43218606 | CAGCAAAGCTGGCTT[C/T]GGGCAACATTTATAC | 23072 |
rs150482804 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | HECW1 | GRCh38.p7 | 7:43293041 | CATCCTAGCTAACAC[A/G]GTGAAACCCCATCTC | 23072 |
rs150483761 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120392 | TCATACCACTTAGCA[C/T]CACGCAATTTGTTAC | 23072 |
rs150485266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514717 | TATCTTTAGGGATAC[A/G]TAATTTAATAATTAA | 23072 |
rs150489834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43406000 | ACCCCCCAGTCTTGC[C/G]CATGCCTCCTCTTCC | 23072 |
rs150498252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43235041 | ATCCCCTGCCAGACC[C/T]GTGGTCCAGACCCAA | 23072 |
rs150503467 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43454198 | GGTTCCTGGAGGGCA[C/G]GGTCATGTGTCACTC | 23072 |
rs150509069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529678 | AACCTTAACACCCTC[A/G]CTGGAGTCCATTCCT | 23072 |
rs150515905 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43349399 | TATAGTTTAAGTCCA[C/T]TGTTTCTTTGTTGAC | 23072 |
rs150533381 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125825 | TGAATGGAGCCAAGC[A/G]GCCTTTTGTAAGGGA | 23072 |
rs150561057 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43524617 | ATTCTCCTGTGAGGT[A/T]AGTAAGCAAATACTA | 23072 |
rs150585829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43294513 | AAAACTAGCTCCTCC[C/T]GGTCTCACTGGATGC | 23072 |
rs150587722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192250 | AGGCGTGAGCCACCA[C/T]GCCTGGCAAGACCTA | 23072 |
rs150591963 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122576 | AACTTTGCAAGCACT[A/C]TCCATCCTGTTGTCG | 23072 |
rs150595449 | in-del | -/G | 0.0744748 | 0.178019 | intron-variant | HECW1 | GRCh38.p7 | 7:43229491 | GGGTGGAGAGTGGGA[-/G]GGGGGAGGGGAGCAG | 23072 |
rs150599871 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43409068 | ATCCTTGACAAGAAA[A/G]CATAATTAGACATAT | 23072 |
rs150624470 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43548594 | TCAGCTACTAGTGAA[A/G]AAGCCAAAAATGACC | 23072 |
rs150624516 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43179525 | AAGAAATACCATTGG[C/T]TATTTGGGAGAATTG | 23072 |
rs150627992 | in-del | -/CTA | 0.039522 | 0.134904 | intron-variant | HECW1 | GRCh38.p7 | 7:43168547 | TGCCTGAGGTCCCAG[-/CTA]CTCAGGAGACTGAGG | 23072 |
rs150631717 | snp | A/G | 3.31257e-05 | 0.00406962 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43469018 | CTACCAGCACAACCG[A/G]GACTTGGTGAATTTC | 23072 |
rs150638662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43290131 | TCTAAGAAAGGTCTG[C/G]AAAGTGAAGGCCTGT | 23072 |
rs150638843 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43188692 | TTAAATGTACTGGCT[A/G]GAAATGACACATGTT | 23072 |
rs150652866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43401437 | ACAAACTGAACAGAA[A/G]CAGTAATAGAAGAAA | 23072 |
rs150655718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43201460 | CAAATTGAGAATCCA[C/T]GCTCAATGGGATGCT | 23072 |
rs150659299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130050 | AGAAAGGCTGATTGT[A/G]TACATTGCAATATGA | 23072 |
rs150663135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43421159 | AGCATCATCGTTTTA[C/T]GACAATAGTGCTGCT | 23072 |
rs150665986 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43496926 | TTGTCCCAGGGCTAT[A/G]TATGCAGTAGCAAGC | 23072 |
rs150671700 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43244583 | ATGAGCTCCTCTCCT[A/G]AGAGGTAGGTATGAT | 23072 |
rs150674303 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146220 | TCCACCTTGGCACTA[G/T]TGACATTCTGGGTCC | 23072 |
rs150675602 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43540912 | CACGGTCTGAAAAAG[G/T]TTCTGGAAAAATGAC | 23072 |
rs150681275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43433602 | CATCATTCTTGCTCA[C/T]AGTGGCCCCAGCGGT | 23072 |
rs150706221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43196511 | ATGATCTCATTCAGC[C/G]TTGGAGTCCAGGGTA | 23072 |
rs150709265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43271703 | ATAAATCATGGATGA[C/T]GGAATCAAATAGAAA | 23072 |
rs150713380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43491496 | TATAGGCGTACCTTA[C/T]CAATGATATTTATCT | 23072 |
rs150718994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43314638 | AACTTATCATCCTAG[A/G]ACCTTAATTTGACAG | 23072 |
rs150757483 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43375098 | TTGTGAAATTTCCTA[A/G]AATTTCCTTCAGTTT | 23072 |
rs150762937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43264957 | GAATACTGAATTTGC[A/T]CCTCCATTTTTTCTT | 23072 |
rs150786837 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43336841 | TTCACTTAAGATAAT[A/G]GCCTCCAGCTCCATC | 23072 |
rs150795076 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160867 | CTACTGTTCCCGCCC[A/G]CTGTGCTGTGCCTTT | 23072 |
rs150803873 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43558918 | AAAGAGTAAATTTAG[A/G]AGGAAAGAGAGCAAG | 23072 |
rs150808907 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43450118 | CTTTCCTGTCGCCGT[C/T]TTTCTGCTTTTTATC | 23072 |
rs150811139 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43369746 | AAGGCTTTTCTCTTC[C/T]TTCTCTGCAGCAGGG | 23072 |
rs150831186 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43285316 | TAAGTCAGAATCCCT[A/G]GAGGCTAGGACCCAG | 23072 |
rs150833111 | snp | A/G | 6.63328e-05 | 0.00575865 | missense | HECW1 | GRCh38.p7 | 7:43508095 | GGAAAGAGCTCCAGC[A/G]AAACAAGCTCTACGT | 23072 |
rs150837150 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111155 | GAGGTAAAAAAATTA[C/T]CCTTTATTGTGGTTT | 23072 |
rs150839419 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43395185 | ATAATTTCTAATCTT[A/G]CAGCTAACGTTAGTC | 23072 |
rs150850149 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | HECW1 | GRCh38.p7 | 7:43223563 | GGTGGAAGTTGAAGC[A/G/T]AGCTGAGATTGCACC | 23072 |
rs150854326 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520110 | ACAAATGTCTTAGAT[A/G]TGCATTCATCAATGC | 23072 |
rs150856336 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43553837 | TCCTGCCAGGAATGT[A/C]CTCCTTCTTCCCTCC | 23072 |
rs150860377 | in-del | -/TTTA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159106 | GCATGAATCTGACAG[-/TTTA]TTTATTTATTTATTT | 23072 |
rs150861238 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43443422 | TTTCAAATTCAGTCT[A/G]TTTCTATATTCTGAG | 23072 |
rs150865270 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43170416 | CGTGGTCCCAAAAAG[G/T]TTGGAGACCGCTGGT | 23072 |
rs150872867 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | HECW1 | GRCh38.p7 | 7:43459729 | TTTTAGTAGAGAGAA[C/G]GTCTCACCATGTTGG | 23072 |
rs150874345 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43378422 | CTAGAACAATCATGT[A/G]GTTTATGAGCGGAGC | 23072 |
rs150878664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43280970 | GACACAGTATTCTCT[A/T]TTCCCGTTTTGTTTG | 23072 |
rs150883650 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43354509 | AACTGAGAAATATAT[C/T]TGCTGAAGTGAAAAA | 23072 |
rs150886183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43181686 | AATTGAATTATTTGG[A/G]TTCTTTGCTATTGAG | 23072 |
rs150893712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389805 | ACCACCATGCCTGAC[C/T]AAATTTTTGTAGAGA | 23072 |
rs150895720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43500911 | TTCTAGTAACTGCAA[C/T]GCAAGTGGGACCCCA | 23072 |
rs150935114 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335970 | TCCTTCCTTCCTTTC[C/T]CTCTCTCTCTCTTTC | 23072 |
rs150941034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116131 | GCTTAAGGGGGAACC[A/G]AGAGCCAGGACTCAA | 23072 |
rs150944972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43333245 | CAAAATGGAGGTCTG[A/G]AAGGAAGATCAAGGT | 23072 |
rs150950122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43398035 | GCCAAGGTGAGCAGA[C/T]CACCTGAGGTCAGAA | 23072 |
rs150956231 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159707 | TTTTTTGAGATGGAA[A/T]CTTGCTCTGTCGCCC | 23072 |
rs150960196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43446240 | TGACTTTGTTTCCAA[G/T]AAGAATCAAATCCAA | 23072 |
rs150963033 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521746 | CAGGCGTGGTGGCAC[A/C]TGTCTGTAATCCCAG | 23072 |
rs150970693 | snp | A/C | 0.0807149 | 0.183963 | intron-variant | HECW1 | GRCh38.p7 | 7:43345984 | CTTTTTCAAATAATG[A/C]CTTCTTTTCCTCTGG | 23072 |
rs150974067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43173345 | AGTCAATAGAAAGTT[C/T]GGGTTTCTCCTGAGC | 23072 |
rs150987704 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43182706 | TGACATTGGTATTCA[C/T]TGGTATTTTGATAGG | 23072 |
rs151001958 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43391810 | AAGGTGTGTTTACTT[A/C]TCTACCATTTACTTG | 23072 |
rs151004257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43220323 | GATGCATTACCCTCC[A/C]AGCACAGAGTATTGC | 23072 |
rs151011465 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517096 | TTAAGAAACGACTAC[A/G]TTATGAGTCACTCTT | 23072 |
rs151025028 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43532927 | ATTGCCTCAGAGGGC[C/T]CAGTCAGCCTTCTTC | 23072 |
rs151029334 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137053 | TCAACCTGTTAGAGT[C/T]AAGCAGTGAGACACA | 23072 |
rs151029893 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43426444 | AAAGGGTCTCTTGAT[G/T]TCACAGGAGGGATCA | 23072 |
rs151035893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43456836 | GGCAGACTGGTCCAC[A/G]CCCATCATACAGTTC | 23072 |
rs151071778 | in-del | -/A | 0.0345262 | 0.126772 | intron-variant | HECW1 | GRCh38.p7 | 7:43454745 | TATATTTTTTCCCTT[-/A]AAAAAAATGAGAGTT | 23072 |
rs151110592 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43194558 | TTTCCGCAAAACCTT[A/G]CTGAAATCAGAGACA | 23072 |
rs151115039 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123811 | GGGTGGGCTGTGGGC[C/T]GGGAGTGGAGGCTGG | 23072 |
rs151119423 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43412013 | TTGTCCTCTGGATTG[G/T]TTTCTTATTTCCCCT | 23072 |
rs151124407 | in-del | -/CA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468099 | ACCACCAGCCCCCAC[-/CA]CACACACACACACCA | 23072 |
rs151129677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43312487 | TAGTTTCCAGCATAA[C/T]CTTTGCCAGCTCTTC | 23072 |
rs151147282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154573 | CTTCTTTACACCTTA[A/G]GTGTATTTGTTTGTG | 23072 |
rs151148306 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43253175 | ATGCACAGCCCGTTT[C/T]GGGAACCACTGGCAA | 23072 |
rs151155425 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43550317 | GGAAAAAAGACTCCA[A/G]GGATAATAATGCTGA | 23072 |
rs151158331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43291628 | ACTATTTCTAACACT[C/T]ACGATTTATTCTTCA | 23072 |
rs151163074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43189758 | GTATTAAATGCATAA[C/T]TACCAATGGAAGTTG | 23072 |
rs151166719 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43264245 | CTCCCCATCCCTCCC[C/G]CTTCCCCCAGCCTCT | 23072 |
rs151170835 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43484934 | TGGATCCCATCTTAG[C/T]AAGGAAATCACGAAA | 23072 |
rs151172324 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43404936 | AGCCAAGATTACACC[A/G]TTGCACTCCAGCCTG | 23072 |
rs151176413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43307525 | GAGTTGTAAGACATT[A/G]GAATCACTGTCTAGG | 23072 |
rs151184712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131796 | CAGGTAGGTGCAGCC[A/G]GGTGACTCCTGAGAG | 23072 |
rs151193619 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43499126 | TCTCTACTAAAAATA[A/C]AAAAATTAGCCAAGC | 23072 |
rs151194030 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43340227 | CCCACCCCCCACCCC[-/T]TTTTTTTTTCTAAGA | 23072 |
rs151195528 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43424173 | GGGCCCTCTTAGCAG[A/G]TCCCCATCTTTGTCT | 23072 |
rs151196304 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43246821 | GAGGAAGTGGAATTG[G/T]GTGGGGGCTGCAGCC | 23072 |
rs151203749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43545475 | AATAATGTACAGTTG[A/G]CCCTTCAAAATGCAA | 23072 |
rs151209612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43361187 | ATGAGATCCATAGTC[A/G]ACCTTATTAAAGCTC | 23072 |
rs151212715 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43435893 | TGCTAGGCCGGGCGT[C/G]GTGGCTCACGCCTGT | 23072 |
rs151220231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43259220 | GGCGAAACCCTGTCT[C/T]TACTAAAAATACAAA | 23072 |
rs151222071 | in-del | -/A | 0.341524 | 0.232644 | intron-variant | HECW1 | GRCh38.p7 | 7:43354188 | AACATATCCAATAAT[-/A]AAAAAAAAAAAAGGC | 23072 |
rs151222849 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43480307 | TCATTGCCTTTCTGA[A/G]TTAGTATCTATATCC | 23072 |
rs151236056 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43175726 | AAACCTTTGTGTAAC[A/G]AACAAGTCATGAACG | 23072 |
rs151243452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43382665 | ATGAATAGACAGTGG[A/C]TCTATCCCACCAGAT | 23072 |
rs151245167 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43493234 | TCCAGCCATTTTTCC[C/T]GGTGGGAAAACACCT | 23072 |
rs151252372 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43316182 | CCACAAAGATCCTTT[C/T]TCTATTATAAACTGA | 23072 |
rs151256488 | in-del | -/AACAAAC | 0.367708 | 0.220556 | intron-variant | HECW1 | GRCh38.p7 | 7:43328319 | AAACAAAAAACAAAA[-/AACAAAC]AACAAAAAAAACAAG | 23072 |
rs151284614 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43202576 | CCTCCCGGGTTCAAG[C/T]GATTATCGTGCCTCA | 23072 |
rs151326304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43451206 | ATTTCTCTGTTAGAC[C/T]TGACTAGTCTTTGCA | 23072 |
rs180676465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214149 | TTCTATAGTTTTTCT[A/G]GTTTTTCATATATAT | 23072 |
rs180687480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43233320 | TAGATTCTATTATGG[G/T]AAAGACAAGAGTTGA | 23072 |
rs180693813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43252837 | GTTTAACAGTAGATG[C/T]AGAATGTGGAAAAAC | 23072 |
rs180694144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43205371 | ATTCTTTCGGCAGCA[C/T]TGAGTTTTCTCAGGC | 23072 |
rs180701304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43171192 | CTTTCTTATGCGGAA[G/T]GAAGATTGTGCCTTT | 23072 |
rs180701586 | snp | C/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43277333 | GACAGGTGAACGGCC[C/G/T]GCATGTCCAAGCTTG | 23072 |
rs180704297 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43301189 | TTCCAGCTGCCCCCA[A/G]CACTGTCTGGCAGAC | 23072 |
rs180704397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43223176 | TCCTTTGCTTTTATC[A/G]TCAAGATATATCTAG | 23072 |
rs180706238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43261506 | AGTTTAAACCCTTGG[A/G]GGTTAAATGCAGCTG | 23072 |
rs180709253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242098 | GAGGGAGGACCAGAT[C/T]CACTTTGCATGTTTG | 23072 |
rs180711543 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43185639 | ACAGAAGTATTCTTT[A/G]CTGATTATTGTATGA | 23072 |
rs180724777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43199717 | GTTATATATTTTTAG[C/T]AGAAAAAAATATAGA | 23072 |
rs180737475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162768 | TATAAACAAAGCTCC[C/T]ATACTACTGTAATAA | 23072 |
rs180744856 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43179737 | ACTGCCTTAATTTAT[A/T]CCTATGGAAAGTTAG | 23072 |
rs180748326 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43192513 | AAAATGACTAAATAC[A/G]TAAAGATAAACTTCA | 23072 |
rs180758065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43524952 | CTGAGGAGGTTTTCA[C/T]GAGAATCAGCGTTAA | 23072 |
rs180758439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43548302 | ATGCAGGTCATCTGC[A/G]AGTTTTTTCAAATTG | 23072 |
rs180760947 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111048 | ACTTGTCAAGTCATC[C/T]CCATGATGGATAGAA | 23072 |
rs180777161 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144485 | AATTTTTCCCCAAGG[A/G]AGATTGGACTCTTCT | 23072 |
rs180787829 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518253 | TAATTCCAACACTTT[A/G]GGAGGCCAAGGCGGG | 23072 |
rs180792465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43498124 | GGAGGTCCCTTACAC[A/C]ACTGGCTATGCATGA | 23072 |
rs180800702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43561184 | CCATGCAGGAGGAAG[C/T]ACATGAAGCAAGCTA | 23072 |
rs180801871 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43432162 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 23072 |
rs180813991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43449664 | CTTTTTGACCCAAGG[A/G]ATAATGGAACACTTG | 23072 |
rs180818760 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488606 | CCCTCGGGATGGATT[A/G]TTTAGTACCAGTACA | 23072 |
rs180823780 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43468039 | GGCACTGGGCCAGTA[G/T]GTGCCACTGGCCCAA | 23072 |
rs180824227 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43537807 | TTTTTAAAAAAGCTA[C/T]GGCTTGTTTGTTGCC | 23072 |
rs180835614 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43507752 | TTAAGCAATATCCTA[C/T]GAGTTGATCAAAATG | 23072 |
rs180848887 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43480242 | GCGCTCTACAATGTG[C/G]TCTTTCCTTGGCAGC | 23072 |
rs180865982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43338572 | TTGTCTAATGTATGC[A/G]ATGAGACTGTCAATT | 23072 |
rs180894852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43411415 | ATATGATGCATTTTG[A/G]TAGGCTTACCATATC | 23072 |
rs180897599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43458641 | TCAGATAACCTTCAG[A/G]TAAGTATCCAGATTT | 23072 |
rs180901863 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43375175 | AGAATTTTTGAACTG[A/C]AGAATGCTATAAACA | 23072 |
rs180921059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43281702 | CTTTTTCTGTTCTCT[C/T]TCTTTGCTTTCTTTT | 23072 |
rs180921829 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43264727 | CGGGCACCTGTAGTC[C/T]CAGTTACTCCGGTGG | 23072 |
rs180924186 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43317564 | CAGCTGACCCTGTCA[A/G]TGCAGTTTGATTCCT | 23072 |
rs180925990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43393110 | CTGTTAAACCATTTG[C/T]CAAGTATGCTCTGTT | 23072 |
rs180944532 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43203091 | CTCTTCACACGGACG[C/T]GCGTGACACTCAGGC | 23072 |
rs180946213 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43348319 | GGTGTTCATACTAGC[A/C]TTGAATAGTCTTTTG | 23072 |
rs180946329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43325951 | TGCCATCTGTCTCAG[C/T]CCGTTGAGGCTGTTA | 23072 |
rs180947420 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43273837 | CCCTTAATATATGAC[A/C]GAAGTTGTAAAATAT | 23072 |
rs180947435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43219507 | CTGTCTCCAACAACC[A/G]AGCTCTCCAAGTGAG | 23072 |
rs180947978 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296179 | AAAGCAGAATACAAA[A/G]ATGTGTGGTCCCAAC | 23072 |
rs180955563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257604 | TAGACCAAGCAGACT[C/T]GATGGGGGATTTATT | 23072 |
rs180955691 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43238011 | CATCATATTGCTTTT[C/T]GTAAAAGGAAAATGT | 23072 |
rs180957942 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43307401 | AATTTAGTGATATCC[A/G]TTGATTTCCCATACA | 23072 |
rs180963238 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43175921 | CAAGTCTTAAATTTC[C/T]CTTACCCACCAGAGC | 23072 |
rs180966383 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159786 | CCAGGTTCATGCCTT[C/T]CTCCTGCCTCAGCCT | 23072 |
rs180979975 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115267 | GTCTGCATTTTCCCC[A/G]TAAGTGAAATTACTC | 23072 |
rs180985064 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43189564 | CTTCTTCTCATAAAG[A/G]TAATGTGAATACCAT | 23072 |
rs180990379 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43228552 | GGAGAAGAACACTTG[C/G]ATGGATCACCAGCTG | 23072 |
rs180998124 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43544041 | AAATAAATTCCAGCT[A/G]GATCAGAAACCTGAA | 23072 |
rs181004415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131389 | CAGCTCACACTGCTG[A/G]GCTTTCCAATGACCA | 23072 |
rs181006346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43208512 | CTATCACTGAGAGTC[C/T]CCAGGGTCTGGGCCT | 23072 |
rs181023268 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140162 | ACTTTGGAATTTTGG[A/T]TTCTGACATCCTTTT | 23072 |
rs181024221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122927 | TTATTTATTCCGAAA[A/G]CATTTCTTGAGCTAT | 23072 |
rs181026262 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147173 | TAGGTAGTTCCCAGG[G/T]AAATATTTTAATGTG | 23072 |
rs181031020 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43182660 | GTGGTTTCATACAAA[G/T]TTTAGGATTTTTTTC | 23072 |
rs181035304 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43428950 | GAATACATATATGTG[A/T]AATATATGTATGTGT | 23072 |
rs181039374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43463440 | TTTAAAAGTCGCCAT[A/G]CTTGAAACTCATCAT | 23072 |
rs181047759 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43485575 | GGTATGGCTATGGCT[C/T]CCAGGCTGCAAACCT | 23072 |
rs181057108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43553368 | TTATAGTATAAAATC[A/G]GTATAGAATGAAAAC | 23072 |
rs181059744 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521815 | TGGGAGGCAGAGGTT[A/G]CAGTGAGCCTAATTG | 23072 |
rs181061831 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43503643 | GACCACAGGGTCCTA[A/G]AATATGTAATCCAAA | 23072 |
rs181091728 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43473385 | GAAACACCAAAAGCC[A/G]TTCTCCAGATGGATC | 23072 |
rs181097739 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43545834 | GGGTGGAGGAGGTGG[A/G]AGGGGGGCAGGAGAG | 23072 |
rs181107666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512512 | ATAAATGTGTAAAAC[C/G]CTGATGAGCTAAATG | 23072 |
rs181114904 | snp | A/C/G | 0.00133588 | 0.0258115 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43493178 | AAGAAACCACACACT[A/C/G]AGGTAAGCCTCGCCC | 23072 |
rs181128483 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43530154 | GTAGAGATGGGGTTT[C/T]ACCACATTGGCCAGG | 23072 |
rs181129357 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43378928 | TTTGCGCTTTGAACA[A/G]GAAAGAAAATAGGGA | 23072 |
rs181140027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43362560 | CTCTCTTCCAGGCCC[A/G]TTTGTTTGGGCATCC | 23072 |
rs181147746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43398609 | CATGTGTATATCTAG[A/G]CTGAAGAAAAAAAAA | 23072 |
rs181157662 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43232485 | CAGTGGCTTCCACAA[C/T]AAAAGCTTATTTCTC | 23072 |
rs181167153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43390345 | GAAATTCCAGACCAG[A/C]CTGGGCAACATAGTG | 23072 |
rs181171998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43408751 | TGCCAGACCTGAGCT[G/T]GAAGCTATAACCTCC | 23072 |
rs181175649 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43278389 | GTCTCTCGGCACATC[C/T]GCAGCTCCCACCCTG | 23072 |
rs181179966 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43454160 | CCAACCTTTGTCTGC[A/G]AAGGACCCCTTTCTT | 23072 |
rs181181019 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43185039 | CCTGCCAGGCCCCAC[C/T]TCCAACATTGGGGAT | 23072 |
rs181183746 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43418718 | TATCTATATTCATCA[G/T]AAGTTAATATTTTCC | 23072 |
rs181186369 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43262425 | ATTATTTCACATATG[A/T]TGAAACTGAGGCTGC | 23072 |
rs181186867 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198925 | AAGAGCTAGCTGGCT[A/G]TTGTTCCTCTGAAGG | 23072 |
rs181187774 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43437570 | ATTCTTGTCTCTTCC[C/T]CCTCTCAAGGATCCA | 23072 |
rs181196393 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43343088 | AAAATAAGTGACTTC[A/G]CAATGGAAGGCTGTG | 23072 |
rs181196834 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43212731 | TTACTGGAATGTCTA[A/C]GTACTCTAACTTACA | 23072 |
rs181200813 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43322794 | CACAAACCTACAATG[G/T]AAGTTTGGTAAGAGA | 23072 |
rs181205254 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111261 | TGGAAACATCACATG[A/G]TTGGTTGCTGTTGCT | 23072 |
rs181205428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152033 | CCTAAAGTGTCATCA[A/G]ACAGCTCATTTACCA | 23072 |
rs181209982 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135707 | AGAGGTTTTTATTCC[C/T]TTTTGATACCTCTGA | 23072 |
rs181211014 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43242315 | GGGAGGTTTGGACCA[C/T]GCTGGAGGAGGCAGA | 23072 |
rs181213101 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302052 | AGTATTAATTTCAAT[A/G]AGGATACAAACTCAG | 23072 |
rs181218619 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127392 | GCCAGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 23072 |
rs181221923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43288488 | TGGTAAATACAGTCT[C/T]TGCTAGGAAAGGGAA | 23072 |
rs181237233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43205830 | CAAGATGATGGGAGA[A/G]TTATAAGTGCCCAGG | 23072 |
rs181256407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269316 | CAGAACCCTCACATA[A/T]TCTGCTCTTTTTGTC | 23072 |
rs181264040 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43192686 | TGCTACCAGCTGGTG[A/G]CAATCAATGTCAACA | 23072 |
rs181264574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145003 | GTAAATAATCTGCAT[A/G]TATGTCCTTTCATTT | 23072 |
rs181266705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43526002 | AAGAAAAATATCATC[A/G]GTAGGTAAATCTTCA | 23072 |
rs181272091 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43549157 | GTGCCATACACTTCT[A/G]CTTACATCCCATTGG | 23072 |
rs181277394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43180630 | TCGACCTCCTGACCT[C/T]GTGATCCACCCGCCT | 23072 |
rs181286634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43251614 | AGCCACCATGCCTGG[C/T]CACAAAATCTAGTTT | 23072 |
rs181305675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43224607 | GGGCAATTGCTCGAG[C/T]CCAGGAGTTCCAGAC | 23072 |
rs181315129 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163215 | GAACAATTTCTCCCC[A/G]TTGCCAAGCTATTGG | 23072 |
rs181318713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118781 | CTGCCTACCCCCAGC[A/G]TTGTCCTTGGTGTCC | 23072 |
rs181332767 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43535945 | CCAAAAACAAAAACT[C/T]GCAACATACTAAAAC | 23072 |
rs181356775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424162 | CATCCTTTTGGGGGC[C/T]CTCTTAGCAGGTCCC | 23072 |
rs181367701 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43393895 | TTAATCCTATACTTT[A/T]AAAAAATATACATTG | 23072 |
rs181369390 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43442473 | GAAAGCACACTGCAT[G/T]GTCATTAGGAAGAGA | 23072 |
rs181369637 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43403182 | AAGAGAAAAACAAAC[A/G]GAAGTTATTAACATG | 23072 |
rs181370986 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359118 | GGCGTGAGCCACCGT[A/G]CCCGGCCCATATCTT | 23072 |
rs181373866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375536 | TTAAATATATATTGT[A/T]TGGCTTATTGCACCA | 23072 |
rs181382748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43457423 | ATAGCAAATGCCTTT[A/G]AGACTTAACTGTTAT | 23072 |
rs181383194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43218782 | TGTATAGAGAAAGTG[A/G]TACAACGAGTGGAGG | 23072 |
rs181386635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43496874 | GGAGGTGGTCCTTCA[A/G]CTAGTGCTTTGATTG | 23072 |
rs181388334 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43478822 | AAATATAAATAAAAT[A/G]CTCTACAAATTATTA | 23072 |
rs181393955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43196717 | TTTCCACAATATGCC[C/G]AGCTACAAAGTCAGC | 23072 |
rs181397570 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43209421 | CTCTCACTCTGGATC[C/T]GGTTCTCTGCCTTTT | 23072 |
rs181407389 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147713 | GGTTCTCCAGTAATG[A/G]CCCTTGATGGTGCTG | 23072 |
rs181418047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43339642 | TTGGGTATGAAATAT[C/T]ATACACTTGAGTTAC | 23072 |
rs181424364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43432430 | AGGTGTGAGCCACCG[C/T]GCCCGGCCCAGTTGT | 23072 |
rs181424508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43326692 | TGCTCTGGAAATGAA[C/T]ATATTGGTGTCTTGG | 23072 |
rs181426982 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43382501 | ATACATAGATTTCAA[C/T]ATCATAGAGAAAATG | 23072 |
rs181427910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43183391 | ATATAATGCAAACAT[C/T]CTCCGCCCTCAATAC | 23072 |
rs181429901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43168517 | TTTTTTAAATTAGCC[A/G]GGCATGATGGTGTGT | 23072 |
rs181442869 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43282155 | CTTAGATCACTGAAT[G/T]TGCCTCTTACGGCTG | 23072 |
rs181443329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132366 | CACTTACTAATAGGG[A/T]CAAATTCCTATTCCC | 23072 |
rs181449131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115586 | CTTGCTAGCGCTGTT[C/G]CTTGTCACAAAAATG | 23072 |
rs181457677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43488962 | TTCTGAAGTTTTTCA[A/G]TCTGGCTCAGCTTTA | 23072 |
rs181459944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43558584 | GTCCATTGAGTAGAA[A/G]CCAAGGATGCTGCTA | 23072 |
rs181464856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43367016 | CTCTGCACAAAGAGG[A/G]ACTTGGGGAAATTTC | 23072 |
rs181476892 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43246266 | TAATATGGCACCACT[C/G]CATTCCAGCCTGCGT | 23072 |
rs181518738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43188138 | GAGGATGTCTCTTCA[A/G]AGGGATTGTTTTCGT | 23072 |
rs181542623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412193 | GAGTTAATTTTGTAC[A/C]ACTTTACATAAAATG | 23072 |
rs181542822 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43450189 | CCTGGCTTGTCTGAT[G/T]TCTCCTCAAAATAAT | 23072 |
rs181567124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332153 | AAGAACTCAGGAGTG[A/G]TTTTCATCTACACAG | 23072 |
rs181572222 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307749 | CTATCCACCTGCTGT[A/G]TTCAAGAAGCAACTG | 23072 |
rs181572550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43399090 | GCAGCCTCCAGCTAT[A/G]TGACTCCTAAATCAT | 23072 |
rs181576014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43438380 | TTACCCAAGAGAGTA[A/G]AAAATCCTATTAAAA | 23072 |
rs181579982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43419305 | ATTCATTCCATGCCC[A/G]TCTCTTGTTGCAGTG | 23072 |
rs181583161 | snp | A/C/T | 0.00676848 | 0.0578101 | intron-variant | HECW1 | GRCh38.p7 | 7:43473710 | TCAAGGGGAGTAAAA[A/C/T]GGGATCATTTAAAAA | 23072 |
rs181586616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43454243 | AGGACCTGGCACAGT[C/G]TCTAGTTCAGAGTGA | 23072 |
rs181589807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43502018 | GAAACCACATGGTCT[A/G]CAAAGCCTCAAATAT | 23072 |
rs181592611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43493825 | AGTACATCTCTTTGA[C/T]GTTTGAATTTTCACT | 23072 |
rs181595484 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43349234 | AGACGGGGTTTCTCC[A/G]TGTTGATTAGGCCGG | 23072 |
rs181603915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43232916 | AACACAAAAATATTC[A/G]TGGAACATTGTTTCA | 23072 |
rs181605817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43229812 | AAAATAGTGACTTTA[C/T]AGTGGAGAAATCTGA | 23072 |
rs181606915 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43311497 | GTATCAAGTGGGTTA[A/G]AGCCGGGAGAGGCAG | 23072 |
rs181608496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43289771 | GTTACAGTTTGGTTT[C/T]ATACATTTTAGGGAG | 23072 |
rs181611499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43252671 | ATAGTCATACCCACG[C/T]ATTTTGTAACCTTCA | 23072 |
rs181615805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43270111 | TTCTTTTGAAATTCT[G/T]TGTGTTATCTGTTGC | 23072 |
rs181620350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43379564 | TTCACCATCATTCCT[G/T]CTGCTCTGCCCTTGC | 23072 |
rs181622869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157254 | TAATCTTTAGGAAAC[C/T]CCAGAGTTTTCATAG | 23072 |
rs181624817 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513127 | TTCCACAAGTCCTAC[A/C]AGTCTCTTCCTTCTA | 23072 |
rs181630323 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43264801 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 23072 |
rs181634542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43363350 | GCAGGTGCCTGATTG[C/G]TACTGCCCTGACCTC | 23072 |
rs181638466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213323 | ACTTTATCATAAATG[A/G]CATGTGCTTATTTTG | 23072 |
rs181648305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121432 | TTGGCCAGCTCATAT[C/T]CCCATGCACTCTTTT | 23072 |
rs181656317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43554262 | TTTGGTCTCTACCAG[A/G]CCCTTCTACTCCTTA | 23072 |
rs181662697 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43201924 | GAGAAGTATGACTTA[C/T]GACTCTGGGGTAGAA | 23072 |
rs181692723 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43446438 | AAGTCACATAATAAT[A/G]TGAAATAATTCAGTT | 23072 |
rs181698927 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43484175 | TGCAAATGGGTGACC[A/G]CTAACGTGTGTTCCA | 23072 |
rs181700060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43179378 | GTGGTAAAAATGGCA[A/G]CCTTTGCTTGAATTA | 23072 |
rs181722630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126243 | GTGCAAACCTTCTTC[A/G]TCATCTATATCTCTT | 23072 |
rs181723798 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43559687 | GCCCTGGTTTCTTGC[C/T]GTCCACTGCCCCACA | 23072 |
rs181730932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43370211 | AACACCTGGATAGAT[A/G]TCTCACCAAAAATAC | 23072 |
rs181731731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162354 | ACAAGGCTCCAGAGC[C/T]CAATCAGTGCCTTTC | 23072 |
rs181732608 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302717 | TTGGGCCCCTGGAGC[C/T]GCACTGTGGTTCTGG | 23072 |
rs181740565 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143871 | GAAGTCTAGAGGGAA[C/T]TAGGTAGTTTTTCTC | 23072 |
rs181750074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530594 | AAGTTTACTGCTTTA[A/T]AAACTTCTCTCCATA | 23072 |
rs181761465 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43343498 | TTCAATTCCCACCTA[C/T]GAGTGAGAACATGCA | 23072 |
rs181764474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43408099 | TGATCCTTGAGCAAG[A/G]GTGTCAAATCTTAAA | 23072 |
rs181769317 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43410723 | GAGTCATTTAGATTA[A/C]CTATTTCTTCTAAGA | 23072 |
rs181774219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43479911 | ACCGGGACACCCACT[A/T]AACACCCCAGAGCTG | 23072 |
rs181777949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43373956 | TTCAACCATGTTGCC[A/G]CGTGTGCCAGAATTT | 23072 |
rs181781461 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43392246 | AACAAACCTTGTCAG[C/T]ATGTTTAGGGGAAAT | 23072 |
rs181784420 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43449315 | GGGTGCCGGCATGAG[A/G]GGAACCTTCCTTGTT | 23072 |
rs181790258 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43431039 | CCTCAGCCTCCCGAA[A/G]TGCTGGGATTACAGG | 23072 |
rs181795341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517978 | TTAGTTAATGATGCC[A/G]GTACTGTAACTGGGT | 23072 |
rs181798385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43497880 | GAGGAAGAATGTCAA[A/G]GATTTTATTTTGGAT | 23072 |
rs181802872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43265747 | TCACAAGGCTGCTCC[C/G]ACTTCAGGCATCAGC | 23072 |
rs181809161 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43537467 | AACAGCTAATGTAAT[C/T]AACTTCCCCACAGGC | 23072 |
rs181817606 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43461777 | CATTTTGTTCTAAGA[A/G]GCCGGCTCAGGAAAT | 23072 |
rs181822267 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358563 | AATGGAAAACCTGAG[A/C]AACTGCAATTAAATG | 23072 |
rs181824902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43230027 | AGTCAGAGCCTGACT[C/T]TTATCACAAGGAAAC | 23072 |
rs181824921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43326887 | GAAGCAGCCAGAGCC[A/G]GAACAAGCTCGCTGG | 23072 |
rs181829766 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308045 | TATATTATATTGTAT[A/T]ATATATAATACAACA | 23072 |
rs181830785 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247493 | TAATAAAAATAAAAT[G/T]TTAGCCAGGCATGGC | 23072 |
rs181831017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43337685 | TCTTCAGATGCTCTT[C/G]CTGGATGGCCTCTCC | 23072 |
rs181831667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283180 | TTTGGGGACCCCTGG[A/G]AGGCCCCCAGAGCCT | 23072 |
rs181843340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43199102 | CTCATTGCACACTCT[C/G]TCTCTCCACGGTTTT | 23072 |
rs181850932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43209873 | GGGCCGGGCATTGGC[A/G]TTCACCCCGAGGTCA | 23072 |
rs181857546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136195 | CAGAGGCGCCTGATA[C/T]TACTATAGACAGGAT | 23072 |
rs181862360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43170789 | AAAGTGGCCCAGCTG[A/C]CCGTGCAAAGGTGGG | 23072 |
rs181915647 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43175398 | TATCCTTTGACCAAC[A/G]TCTTTTCCATCTCTT | 23072 |
rs181919000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43457557 | GCGGGTGGATCATTT[A/G]AAGTCAGGAGTTCGA | 23072 |
rs181927694 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43555161 | TCGAGCATCGTTATC[C/T]GTACTTCTGCAGCGT | 23072 |
rs181929171 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122548 | AACTTTTTGATGAGA[A/C]CTCTCTCATAAGAAC | 23072 |
rs181933286 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158594 | TTCATGAACACCTTT[C/G]ATGTGGATATTCTCC | 23072 |
rs181933864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43323445 | CAGAAAATTAGTCAC[A/G]TATGATGATGTATGC | 23072 |
rs181939498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43353425 | AGAAGAGTACCATGA[C/T]GTCCATTTCCAAAAG | 23072 |
rs181939988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139712 | TTTTATATTGTTCCC[A/G]GCTTCTAATCTTTTA | 23072 |
rs181961805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43408590 | ACTGGAGAGGCTGAT[A/G]TGGGAGGACTTCTTG | 23072 |
rs181975086 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43349501 | TCTATATCATTTCTT[A/T]GGTCTATTAGTAATT | 23072 |
rs181977626 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43389615 | TCTCATCACATTGTT[G/T]TTGCTGTTGTTGTTG | 23072 |
rs181981619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424516 | TAGTTCCAGGTACTC[A/G]GGAAGCTGAGGTGGG | 23072 |
rs181985035 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43446878 | ATGCCTTTCTTTCAC[A/C]AGGATGTTTCGAGGA | 23072 |
rs181985443 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513668 | CTGGAAAAAAAAACT[A/G]TTTGTGGGTTTTGGT | 23072 |
rs181987926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43383142 | GCAGCATAGTATTCC[A/G]TGGTGTATGTGTGCC | 23072 |
rs181988804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530961 | CAATGGGTTCTCATC[A/G]TCTACAGTTTAAAGG | 23072 |
rs181989944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428684 | ATGACAGTTTATCAA[C/G]AAAGCACGTGCAGAA | 23072 |
rs182003785 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43312313 | ATGAGATATAGCAGA[A/G]TCAGGTGTGGTTAAA | 23072 |
rs182012238 | snp | A/C/G | 0.00637319 | 0.05614 | intron-variant | HECW1 | GRCh38.p7 | 7:43273560 | TTTCCTCTTTTACCC[A/C/G]TACCTCAATCCCTGA | 23072 |
rs182014664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427847 | CCATTGATGGAGAAT[G/T]TCCCTTGCATTGAAT | 23072 |
rs182016592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43389026 | GGGGATGCAAAGAAG[C/T]AGGTCATTGTTTCTA | 23072 |
rs182023760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43353934 | TCAGCAGCACCATGC[C/T]GTGGAAAGCTTGTTC | 23072 |
rs182027372 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43370676 | ATTCAGTACTAAAAA[A/G]AAATGAGCTGCCAAG | 23072 |
rs182031101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332611 | CGGTGTCCAATTACA[C/T]AGACAGACACAGCAG | 23072 |
rs182043749 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316666 | AAGAATGCAGAAAAT[A/T]ACAGCCTCCTGGTAG | 23072 |
rs182047475 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43194223 | GTTCAGTCAGTTGAG[G/T]GGCTTGGAATTCTAT | 23072 |
rs182056578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43278736 | AGTGCTTTTTCCCTT[A/G]AGGTCTAAGTTGTCA | 23072 |
rs182062073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206483 | TCTTTCCTCCCCTCA[G/T]TCCCCCACTAGCTTG | 23072 |
rs182066636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43237792 | GGATAACTGGTGACA[A/G]ATTTTGAAAATAGAG | 23072 |
rs182088539 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43185240 | GGGCATGGAAAGTCC[A/G]CTCCCCATGCCCCAG | 23072 |
rs182101575 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43202654 | AATTTTTGTGTTTTT[A/G]GTAGAGATGGGGTTT | 23072 |
rs182126561 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153771 | CTTTGTATAGTAAAC[A/G]TGGAGACAGTAACCC | 23072 |
rs182134680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136535 | GAGAGCTGGCAAAAA[C/T]GGGTCACTTCTGGAA | 23072 |
rs182143957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119209 | AGGTATCAGTCACTC[A/G]TTCCTGTCACTCCCC | 23072 |
rs182146693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118841 | TATAAAGAGGATGAT[A/G]ATAAGGAAATAATTG | 23072 |
rs182147274 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154057 | TTTAAAATTATTTCT[G/T]GGATTTGCAAATAAT | 23072 |
rs182158599 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43404635 | TTGAGAATTTAACCT[A/T]TGCCAAAGTTGACAT | 23072 |
rs182171890 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43424859 | GGATTTTTTTAAAAT[G/T]TTAAGCCCAGAATGG | 23072 |
rs182175780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43503036 | TCTGGTTCCTCCAAG[C/T]TGTAGCATTCAGAAG | 23072 |
rs182176786 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43383555 | TGAGCTTTTTTACAT[A/T]TGTTTATTGGCCACA | 23072 |
rs182186896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43451723 | GAAATTGATACCCCA[G/T]ACATTATATATTCAC | 23072 |
rs182195119 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43490291 | TGCTCCCATTCCCCA[A/G]CCGTAAATGCTGCCT | 23072 |
rs182197492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43470201 | TGGGAGAGTGACAAT[A/G]ATTTGTATGTGGGGA | 23072 |
rs182202049 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510351 | GTGTCTTAGAGATCA[C/T]GAATTGGAATCAGCA | 23072 |
rs182204615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43543422 | AGAATGCTGTCTTAC[A/G]TATTTGAGAAAAAAA | 23072 |
rs182205817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43443007 | CTAGTAACTAGATAT[A/C]GACTAGCCAGTTGCT | 23072 |
rs182208693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43259805 | TTTAAAAACACTTTA[C/T]CCATCATCAATCAGT | 23072 |
rs182225580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43220926 | CCCTGTGCAGACCAT[A/G]TGTGGCTGGTGTCAC | 23072 |
rs182225973 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155312 | ATTCTTAAAAATAAA[A/C]AATAAACAGAGAATA | 23072 |
rs182227573 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43350001 | TGTTTTGACGTGTTT[C/T]CAGGATTTGTTTCAA | 23072 |
rs182229044 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43368206 | GACAGACAAGAAAAC[A/G]GGCAATGACAGAGCA | 23072 |
rs182231900 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43240071 | TCTTTTGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 23072 |
rs182236487 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299454 | AAAATTGAAAATACT[G/T]TCCAAAATCCCACAG | 23072 |
rs182240054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43527311 | ACTGGCCATTCTCAG[C/T]TCTGGAAGCCAGAAG | 23072 |
rs182241395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43327419 | CACTGTGTAACGGTC[A/G]TGAAGTAATTCGTGT | 23072 |
rs182243861 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43275186 | TTAAAAATCCAACAA[A/C]AAGTTTACTTGAAAT | 23072 |
rs182247507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550158 | CCAGGCGGAGTGGGG[A/C]TTGTCTGTGGTCCCA | 23072 |
rs182256846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203855 | TTTTGCAGTTGTATA[C/T]CCCACTTTCTTAAAT | 23072 |
rs182267850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43463185 | TATTTATTTGCCAGC[A/T]TGCTATCAGATGTAA | 23072 |
rs182275531 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43467279 | GAGTGCTCTGGGGGC[A/G]CCAGGGAGCATTCTT | 23072 |
rs182283470 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43404007 | ACTTTTGGAAAATTC[A/T]AGAACTCTATGTGCT | 23072 |
rs182291274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295737 | TTGTTTATATCCCAC[A/T]ATCTCTCAGTCTCAT | 23072 |
rs182300758 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43291251 | AAAGGAAAAGCAGAC[A/T]TATTTATCCTTTACG | 23072 |
rs182301039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43322250 | TTTTTAGTAGAGATG[A/G]GGTTTCAGAATGCTA | 23072 |
rs182317652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43397279 | AACAGATAACTGAGC[C/T]GCTCAAAAATGCTCA | 23072 |
rs182331429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43361917 | AGTCCCCAGGCAGGC[A/G]GATCACTTGAGGTCA | 23072 |
rs182354202 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43219213 | AGAGGACAACAGTGG[A/G]AATCGCCATGTTGGG | 23072 |
rs182371659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420281 | GTCTTTGAAGAGGAA[A/C]CTCTACTTTACTTTT | 23072 |
rs182373048 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43257198 | AATATTCCAAAGTGA[A/G]CTATTAGTAGTTGGT | 23072 |
rs182377466 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43380548 | ATTTTTTCCCCCTAG[A/G]TGAAGTTTTGCTCTT | 23072 |
rs182383931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128864 | GGATGATTTTGAAGG[A/G]TTCAATACCTCAGTG | 23072 |
rs182383999 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43400616 | CTCAACAAAATAGAG[A/G]GAAGTGCAGAGCATA | 23072 |
rs182391321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189109 | GTTTGCCCAAGCTTG[A/T]TTATGCCAGTAATAC | 23072 |
rs182404491 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43165355 | GAATTATGTTACATA[C/T]CATGAGGTTAGAAAA | 23072 |
rs182408906 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148431 | TGCCTGCATGTCTCT[C/G]TGTCCTCATGCCCAA | 23072 |
rs182411037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43304717 | CAGGCTGGTCTCAAA[C/T]TCCTGGCCTCAGGTG | 23072 |
rs182414424 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43279775 | AAGTATATTTTTATT[G/T]GTGTATTTGTTTCCT | 23072 |
rs182420022 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116649 | CCTGCTTCCTTTTCC[A/G]TCCTAAAAAACAGGA | 23072 |
rs182431823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43364180 | AAAGGAGGAACAAGC[C/T]GTCACATGCTCCTTT | 23072 |
rs182437172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131206 | AGGAGCAGAGGTTGC[A/G]GTGAGCCGAGATCTT | 23072 |
rs182438067 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43346053 | GTTCTATTTTTAGTT[A/C]TTTAAGGAATTGCCA | 23072 |
rs182439281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43323988 | GCAGTGAGCCGAGAT[C/T]GCACCATTGCACTCC | 23072 |
rs182441179 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562793 | TTGTCTTATGTAGAA[C/T]GTGGCAATGCCAACT | 23072 |
rs182444574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43485008 | GTTGACATCAATAAG[A/G]AAGGATAAGCAGAGC | 23072 |
rs182451791 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43487430 | CTAAAAGTAGTCCCT[A/G]CTACAAACTGGGTTT | 23072 |
rs182459047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521274 | GCCTTGAGAGAGTGA[A/G]TTTGCCCACTAGGTA | 23072 |
rs182476980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43504892 | ATCTCTGGAGGTCAC[A/G]AAAGGAGGTGTCCTC | 23072 |
rs182486467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523595 | AGTGAGCAGAGATCT[C/T]GCCATTGCACTCCAG | 23072 |
rs182486552 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43546918 | TAAGGGACCTTTGTG[G/T]TGCTTTTTTTCCAGA | 23072 |
rs182536092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376836 | GTGCCATTGCACTCC[A/C]GCCTGGGTGACAGAG | 23072 |
rs182546561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43340244 | TTTTTTTTCTAAGAC[A/G]GAGTATCGCTCTGTC | 23072 |
rs182553617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43443444 | TATTCTGAGAATACA[A/G]CTGACTCTTCCTTTG | 23072 |
rs182559081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43342757 | GAGGCCGGGCATGGT[A/G]GCTCACGCCTGTAAT | 23072 |
rs182570618 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43270913 | GAAAAGAAGTATGTG[A/G]AAACTCTCTGAAGAA | 23072 |
rs182571877 | snp | C/G | 0.00288037 | 0.0378403 | intron-variant | HECW1 | GRCh38.p7 | 7:43444177 | TAACACCACAATGCT[C/G]TCTTCTGGGAGAAAT | 23072 |
rs182584710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43253270 | TTTGAGAGAACTGAA[C/T]GGTAGCATGAAGGGA | 23072 |
rs182585327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425066 | TGATTGATAGAGTAA[C/T]CAGAAGGGGGATATT | 23072 |
rs182587410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43459082 | CATGGCAGGAAAATG[C/T]CTCCCACCTGCCTCC | 23072 |
rs182594846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43266388 | TCACTCAGGCTGGAG[C/T]GCAGTGGTGCGATCT | 23072 |
rs182602024 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43378568 | CTAGCACTTTGGGAG[G/T]CCAAGGCGGGTGGAT | 23072 |
rs182607035 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43481065 | GCATGCTAAATCTTT[C/G]TTTCTTCATATATAT | 23072 |
rs182609809 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43200033 | TTTATAAATCCTTTT[A/G]GGGCTCATGCCAAAA | 23072 |
rs182612307 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43181227 | GTGTATATATACCAT[A/G]CTTTATCCATTCATG | 23072 |
rs182612824 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43499417 | GAGGTTGCAGTGAGC[C/T]GAGATTTTACCACTG | 23072 |
rs182612997 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214787 | GGAGGAGGAACCCCC[A/G]GAGAGGGGCCAGCTC | 23072 |
rs182616165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518826 | TATATCACCTTATAA[C/T]GATCAAATTGCCAAA | 23072 |
rs182623071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43233873 | ACAATGGGCATAATA[G/T]AAGCTGTGATAGCCT | 23072 |
rs182631497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43172085 | GCGTTCAAAACCAGC[C/T]TGGCCAACGTGATAA | 23072 |
rs182633102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43230159 | GCACTTGGGGAGACC[A/G]AGGCGGGAGGATTGC | 23072 |
rs182638256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145561 | CTTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 23072 |
rs182648082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43186438 | TTTGGGAGGCCGAGG[C/T]GGATGGATCACGAGG | 23072 |
rs182648588 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43404957 | CTCCAGCCTGGGCAA[A/C]AAGAGTGAAACTCCA | 23072 |
rs182650842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43169450 | GTCTCCAGACATTGA[C/T]GGATACCCCTGGGAG | 23072 |
rs182654099 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145956 | TGCACAGTGGTATGC[A/G]GTGAGAAGAAGCCAC | 23072 |
rs182659019 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43197505 | CCCAAGGAGAGGGTG[A/G]GACCCACCTCTTGGC | 23072 |
rs182671545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155319 | AAAATAAACAATAAA[C/T]AGAGAATATACCAAG | 23072 |
rs182682205 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43112947 | GCCAAGGTAAGCGGG[A/C]GTAGCGCGGGGACAC | 23072 |
rs182727989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43494989 | AGGACATCTCATCCC[A/G]TTTTAAAGGCTCAGA | 23072 |
rs182737145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43531957 | CATCTGCATCCTGAC[A/G]GCCCCACAGTGACAT | 23072 |
rs182801621 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43439941 | AGCAAGCCATGGAGG[C/G]GTTTTTCCTCCCACC | 23072 |
rs182810424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421094 | CATTGGCACAGAACA[A/G]ACAAATAGCTAATTA | 23072 |
rs182815270 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43274169 | ACGCCATGAAGGCCT[C/T]GGGTGCACTAAAAGA | 23072 |
rs182817673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43360566 | GAAACAGACAGGTGA[C/T]AGGCATCCACCCACC | 23072 |
rs182817974 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43455142 | CTTTTTTTTTGTTTT[A/C]TTTTGTTTTTAATTT | 23072 |
rs182818890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43455280 | GATATTTGACAGCTG[C/T]GTGTTGAATATACAC | 23072 |
rs182820152 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43258355 | CTCAAAAAAATAAAA[A/C]ATAAAAAAAATAAAA | 23072 |
rs182825601 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43495563 | TTTGTGCCCACTCTG[C/T]CCCTTACAACCTGGT | 23072 |
rs182829722 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43475963 | TTATTGTACAATCGG[A/G]TCTAGTAGTTTTCCC | 23072 |
rs182836426 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43544770 | AAGTAGTGAAATCAT[A/G]TGGGGTTATTAAAAA | 23072 |
rs182836997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210997 | AGCCGATGCCGGCTG[A/G]AATGCCTGGGTTTGT | 23072 |
rs182837496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43312654 | AAGTTTACTAGAAGA[A/G]ATTGTTCTATGTGAA | 23072 |
rs182841546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43231249 | TCTGTCCTTTCCACA[G/T]CTGGGAATCATATGT | 23072 |
rs182842143 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43434718 | GAGAGGTTGATGTCT[A/G]GGATGAAGGGATGGG | 23072 |
rs182843992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43394883 | GGACAGAGTTTTTAA[C/T]GATAACTTGGTGGGG | 23072 |
rs182844593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514947 | CAGGTATCATGGCTC[C/T]ATCATCAGGATCTAG | 23072 |
rs182846079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43318206 | CAGAGTGGAGAAATT[C/T]GGGGAAATACTATCC | 23072 |
rs182849991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296890 | GGCACTTAACATGCA[A/G]TTGTTGTTGAAATAT | 23072 |
rs182851373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43249262 | ACTGTCCTGGTGAGT[C/T]GCTCACAGCCTGTCC | 23072 |
rs182863942 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43169775 | CTCACTGCAAGCTTC[A/G]CCTCCCGGGTTCACG | 23072 |
rs182864796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43284205 | TCCCAGATCTGAAAT[A/C]ATTTTCTTTTTTAAA | 23072 |
rs182867203 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43184104 | CTGCAAGCTCCACCT[A/C]CTGAGTTCACGCCAT | 23072 |
rs182868755 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198159 | TCTCTCACACTCATA[C/G]TCACGCACACCCCAC | 23072 |
rs182871689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43401126 | AGGTAACATATTCAT[A/G]GGCTCCAAGGATTAG | 23072 |
rs182879523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43320542 | CTGTTGAGATGGAAG[C/G]AGCATTTGTATCCTT | 23072 |
rs182887131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148827 | TACAGATTCTGATCT[A/G]GTAGGTCTGGGATAG | 23072 |
rs182894893 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134308 | CTGAAGCAGAAGAAC[C/T]GCTTGAACCCGGGAG | 23072 |
rs182901260 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43243779 | GCCAGGTATCTTGGC[A/G]GGGGTGGGGGAAACA | 23072 |
rs182904297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210201 | ACCTTGCTGACCAAG[A/G]ACTCTCTTAACTGGA | 23072 |
rs182909220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43181498 | CTCCACACCCCACCA[A/G]CACTTGTTTTCTTTT | 23072 |
rs182919404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248245 | GCTCCTGACAGCAAC[A/C]CCCCTCTCCTGACAC | 23072 |
rs182922779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43271149 | TTCCACAAATTATCT[A/G]GAAGACTGAGTGGAA | 23072 |
rs182934727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207109 | TGGAGTCCAGTGGTG[C/T]GATCTCAGCTCACTG | 23072 |
rs182949990 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43193192 | AGTGAATAATGAGCA[C/G]TGAGGACTACTAGAA | 23072 |
rs182964976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206050 | TATACATTGTCTGGC[A/G]CTATAGGCTGTGGCT | 23072 |
rs182977642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119577 | TTCCAAGTTTATTTC[A/G]TCAGCCCTGACTCAT | 23072 |
rs182979936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145322 | TATATTTGAGACAGG[A/G]TCTCGCTGTCTTGCC | 23072 |
rs182985393 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43181057 | CTCTTCTTCTATGAG[A/T]TCAACTTTTTAAGAT | 23072 |
rs182990248 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43164820 | TAGAAAGGAGATGCC[A/G]AGCATGCAGCCGCGC | 23072 |
rs182993200 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112095 | CCTTCTCGTTCTAGC[A/G]TTCTGACACTGTGTG | 23072 |
rs183003297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43539025 | GTAACTTTCCAGTTT[A/G]TAACCAAAAAAAAGT | 23072 |
rs183007318 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511334 | GAGCCCACGGTGATG[A/C]GATTTTCTTCAACGC | 23072 |
rs183012490 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43355389 | GCAACCTGTTAAGAG[A/G]TAAGTAATATAAAAA | 23072 |
rs183016611 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514529 | CCTGACCTCAGGTGA[C/T]CCATCCTCCTTGGCC | 23072 |
rs183030426 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43556611 | GAGGATGACTTGAGC[C/T]CAGGAGGCTGAGGCT | 23072 |
rs183032078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550341 | ATGCTGAATAATGCC[C/T]TGTAGAGGATTTTTG | 23072 |
rs183036967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43500253 | TACAGGCAGGCAACA[C/G]CACACCTGGCTAATT | 23072 |
rs183040753 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43293289 | CACAGTGTGGGAGCA[C/G]ACCCGAGCAGCGGTT | 23072 |
rs183045281 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519534 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCTAGTGC | 23072 |
rs183045559 | snp | A/C/G | 0.00518061 | 0.050666 | intron-variant | HECW1 | GRCh38.p7 | 7:43540280 | CACCACTAAATCCCC[A/C/G]ATAAGGTGAAAACCT | 23072 |
rs183047465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43271334 | CTCTCACCTATTCAA[C/G]ATAGTACTGGAAGTG | 23072 |
rs183059413 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562216 | ACCTCCATTACTAAC[A/C]ATGAAATATGAATGC | 23072 |
rs183061886 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43254305 | AAATAATGAAGCCCC[A/G]CTTAAGTGAAAATAA | 23072 |
rs183065492 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43333405 | GGTAAATCCAGAATC[A/G]CCCCTGTTTTGGTGC | 23072 |
rs183069097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43314767 | AAATCCGAAATTGTC[C/T]GTGAATCTTAAAAGT | 23072 |
rs183092100 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43435757 | AAGCCCCTGAGACTT[A/G]GAAGTTGGCTGTTAG | 23072 |
rs183096115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43470576 | GATGCACTGTGAGAG[A/T]TTTGTTCCATTTGGG | 23072 |
rs183103110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439670 | CGCTGCAGCCGCAGA[G/T]CCCCTCTGCCCTCCC | 23072 |
rs183115109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43474798 | TGCAATGAAATGTTT[C/G]TCCTTACAAAGAAAT | 23072 |
rs183119719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328395 | CCTTCAGCAATCCCA[A/G]TCAAGGCCTGCAACA | 23072 |
rs183139933 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43333082 | GGTGCAAAATTCTGG[C/T]CCCATAGAGAGCTCA | 23072 |
rs183145756 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43368466 | TCAGACTAATTTCAG[G/T]TTTGATCAGCAGTGG | 23072 |
rs183146077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43263730 | AAGGGAGGGAGGAAG[G/T]TGGGAAGGAGACAAA | 23072 |
rs183159760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43370837 | GTTGTGAAGATTTAG[C/T]GGGGAAGGATGAATA | 23072 |
rs183174836 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43190302 | TGTTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT | 23072 |
rs183179337 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43225961 | TATTTTTAGTAGAGA[C/T]GAGGTCACAGTATGT | 23072 |
rs183195330 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160378 | TGTGGTTTAGTCTTG[C/T]GGTTAGAAAAATGAG | 23072 |
rs183195894 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43293050 | TAACACGGTGAAACC[C/T]CATCTCTACTAAAAA | 23072 |
rs183202930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142023 | CACACGCTGTGCTTG[C/T]ACTGGAGTCTGTATT | 23072 |
rs183205394 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43178073 | GGAGTGCAGTGGCAT[A/G]ATCTTGACTCACTGC | 23072 |
rs183209106 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43197176 | AAAATAGTTTTTGTT[C/T]TGTGTACACTCAAGA | 23072 |
rs183210593 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43285605 | GCTTGAGCCTAGGAG[A/T]TTGAGACCAGCCTGG | 23072 |
rs183223918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43432840 | TAAGTTCAATTTATA[A/G]AAGTTCTGTTTAGAG | 23072 |
rs183224651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412453 | TTTATTTATTTATTT[A/G]TTTATTTTAATTATT | 23072 |
rs183230388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124452 | ATAGAATGCTGTCTG[G/T]ATAAGGAACCTAAGC | 23072 |
rs183242172 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166311 | TGGTCACGAACTCCT[A/G]ACCTCAGGTGTGTTC | 23072 |
rs183243315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43220039 | TTCGCAAGTCAACAC[A/G]GTCCCCCACACACTG | 23072 |
rs183243517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43469195 | AGGAGAGTGTGGGGA[A/G]GAGTTATGTCTGAGA | 23072 |
rs183246615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43451000 | GTCAGTATGAATTTG[C/T]GTGTAAACATCTAAA | 23072 |
rs183250753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160235 | TATATGTAAAGAATT[A/G]CCTTTTATACATATT | 23072 |
rs183272509 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375911 | AAAAAAAAAAAAGGA[A/T]AAAAAGCTCTTTAAA | 23072 |
rs183274742 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43189895 | TACAGTAGCAGACCT[A/G]CAACATATTTTGAAT | 23072 |
rs183279475 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43351260 | CCAGTGCCTGTTCTG[A/G]TGGAGGTGGCAGAGG | 23072 |
rs183279653 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43328952 | TGCTGGAGGCCTGCT[G/T]GGGATCGTGCTGGTC | 23072 |
rs183281064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43394329 | GGAATAACAGACATA[A/G]AGGAGGAGGGAGAAG | 23072 |
rs183285228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43491142 | GTTTTGTCAAAATGC[C/T]TAAGCTGAACCAAGA | 23072 |
rs183288474 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43561531 | ACTCATTTGCAAATC[A/G]GGCTGATACCATAGA | 23072 |
rs183291189 | snp | A/C | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359639 | TCTCAATTATGCAAA[A/C]ATCTCAGAAGATTGT | 23072 |
rs183294717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43528683 | CACGTTGAGGGGAAG[C/T]AGCTCTGGTCTCACT | 23072 |
rs183297128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43557378 | GCCACAGCAAAACCC[A/G]GTCATAGCCCAGGCT | 23072 |
rs183310025 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123781 | TGGAATAGTGGTACC[A/G]TAGCCCTTCCAACCG | 23072 |
rs183329219 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43486061 | CCCCTCCCTGTGTCC[A/G]TGTGTTCTCATTGTT | 23072 |
rs183344086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43452328 | CAGTACAGATGACTA[A/G]TTATACATGCAAATA | 23072 |
rs183370155 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350423 | GTCTCTTGCAAGGCC[A/T]GGGAAGTTTTCCTCA | 23072 |
rs183390728 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43308656 | TTGAGACGGGGTCTC[A/G]CTCTTGTTGCCCAGG | 23072 |
rs183418877 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43385257 | TCCCTCTCCCCTCCC[C/T]TCCCCTCTCCCCTCC | 23072 |
rs183420102 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43263025 | AATTGATATCAAAAT[A/G]ACAAGAGTGGTTATG | 23072 |
rs183422069 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43409172 | TTCCCAGAAGAGCTT[C/T]GTTAGAGCTTTGAAG | 23072 |
rs183425137 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43447679 | ACTGTCCTTCACTTG[A/C/G]CACCAGGCTTCACAA | 23072 |
rs183429861 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43380939 | TACAAAGTGGTTTTA[A/C]AAATTTACACTTCCA | 23072 |
rs183438662 | snp | A/C/G | 0.0142839 | 0.0833853 | intron-variant | HECW1 | GRCh38.p7 | 7:43225397 | ACTGCACCAAGAGAC[A/C/G]TGGGCTTGTGCATAC | 23072 |
rs183439403 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43239317 | ATCCCCTTCAAAATA[C/T]GTGCAACTGAGCTTA | 23072 |
rs183441481 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303198 | CAAATAACCCAGAGC[C/T]GCACCAAGCAGTCCT | 23072 |
rs183444306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43243513 | ATATGTGAGGATGCT[C/T]TTCGCTGGCCTTCTC | 23072 |
rs183448594 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43447917 | GATTGCCTGAGGTCA[A/G]GAGTTCAAGACCAGC | 23072 |
rs183451339 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43279171 | AATTTGTGCTATGTG[C/T]AAGGGCATTCCCCTT | 23072 |
rs183451784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43409232 | AACTTCCTCCTAGCG[C/T]TGGTTATCAACAGAT | 23072 |
rs183452834 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43429758 | AAAGCACCATGTCCA[C/G]TCCATTTAATTTCCA | 23072 |
rs183455310 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43474373 | AGAATGGCGTGAACC[C/T]GGGAGGCAGAGCTTG | 23072 |
rs183455637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156757 | GTCATGTGATCTGCA[C/T]TGGCCAGTGGAATAA | 23072 |
rs183456447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43267261 | CAATAAATTTCAAAA[A/G]GGAGAAATTATTGAA | 23072 |
rs183460705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43464783 | TATGCTAACTAAACT[A/G]ACTAGTTTAGGTTTT | 23072 |
rs183463825 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43494560 | CTGGGCTGAAGTGAG[A/T]TGGTACAATCTCAGC | 23072 |
rs183472350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43203265 | TGCAACATGCTACAG[A/G]AAGTTGATGTTCCCT | 23072 |
rs183474737 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173598 | ATGCAACCTAGATCC[C/T]TCTCATGCGCAGTTC | 23072 |
rs183487728 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43200325 | CCTTTGTAATATGAT[A/G]CAGTATTTTTAAATC | 23072 |
rs183490052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43334931 | AACTTCTGTTCTTTT[A/C]TTCATATTTACCCTC | 23072 |
rs183493362 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117122 | AGATTTGTGGCATTT[C/T]TTGTTCCCAGTGAGG | 23072 |
rs183493871 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121075 | CCTACAAGGAGGTGG[A/C]TGGGGTTCTTCCTTC | 23072 |
rs183505341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43177320 | GTGGTGGGGCCTTCC[A/G]CAGTGAATCTACCAG | 23072 |
rs183507196 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43472154 | TATGTGAAATCTCAT[A/C]ACTGATATGGCGTAT | 23072 |
rs183511406 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43533278 | GAACTTAACCCATGC[A/C]AGTCCTGGTCCATTA | 23072 |
rs183513411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43492858 | CTGAAACGTTAAGGA[C/T]GATTAACAGAGATCT | 23072 |
rs183514470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512402 | GGTCAGCTTCAAAAG[C/T]TGTTGTTGGTTTTTT | 23072 |
rs183515422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43371975 | CAGGTGCCCACCACC[A/G]CGCCCCGCTAATTTT | 23072 |
rs183517423 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43529591 | TCCACTGTGAGATGA[C/T]TTCAGACCCTACTGA | 23072 |
rs183521535 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43391197 | TCACTTACATCTTTA[C/G]GTGAATGCACACTTA | 23072 |
rs183521726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43356350 | GGTCAATTCAGCAAG[C/T]GGCTATGAAAATCTA | 23072 |
rs183525663 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43262652 | TCAATGCAGTAATGA[A/G]GTTAACATGCATTCC | 23072 |
rs183529673 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43552489 | ACAGTTTTGTGCAAC[A/C]ATTGCCTCTAGCTAC | 23072 |
rs183533365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43173056 | AGACACCCAACTCCT[C/T]AAAGCTAAAGTTCCT | 23072 |
rs183535021 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43225082 | GGTGTGGGGGAAGAT[C/G]ACAGGTGACACATTG | 23072 |
rs183538692 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141560 | GCTAGAGTGCAATGG[C/T]GCAATCTCAGCTCAC | 23072 |
rs183577650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43463942 | TGGAGGACAGAGGCA[G/T]GCCTGGTGCCCGCAA | 23072 |
rs183579023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43504127 | GTGGCCCCTGCCTTG[C/T]AGTCTTCCTCTCCTT | 23072 |
rs183595629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43526432 | TAACTTATGATTCAT[A/G]GAAAGATTGAATGAA | 23072 |
rs183597971 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43460082 | GCTTATTGCTTTTGT[C/T]ACTGTTTTTTGTCAC | 23072 |
rs183615561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43390596 | ATATGAACAAAATAT[G/T]AGCAAAAGAGATGCA | 23072 |
rs183640578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43385952 | AGTTCTCATCTGGAA[G/T]TTCTGTGGAAAAGCC | 23072 |
rs183661704 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151750 | ATAGAAGTGACTGAG[A/C]GGATAGATTTAGTGT | 23072 |
rs183667876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43190934 | AGTATTAATACCATT[C/T]TGTGAAAGACAAGAA | 23072 |
rs183678081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43170294 | ATATATTACAATGTA[A/G]TAATAGTAGAAATAA | 23072 |
rs183680270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43426074 | CAAAATTTTCTTGCT[A/G]ACAAGCTGTCTGATG | 23072 |
rs183683661 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43489809 | ATGCCTGTGTTTGTC[A/G]TTAGGGATCGTTAAG | 23072 |
rs183692110 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426584 | AAATGTCTTTCATTT[C/T]CTTTCTTATGCTTAT | 23072 |
rs183694455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135634 | TAAATTATCCATCTA[C/T]ACCTATCATCTTTTC | 23072 |
rs183697985 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319363 | CTGGAGTCCGCAGTC[C/T]GGCCTGGGCGACAGA | 23072 |
rs183701984 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43178616 | GGTCACTGTGCAGAG[C/T]GCTGCCTCCTCACAC | 23072 |
rs183707875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43406363 | AGCCCTTTCACAGAG[C/T]AGTAATACATTATCA | 23072 |
rs183707876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43445770 | GCTGACACCCCACAA[C/T]GTCTCAGATACACAC | 23072 |
rs183709556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118480 | CTTGCCATCAGTGCC[A/G]TCAGTACCAGAGCTG | 23072 |
rs183730299 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43243050 | AGCTTCAGGTTTCAT[C/T]GGGGTTTGGGAATGC | 23072 |
rs183736885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43330374 | GAGGCCACATCATAC[A/G]TCTAGCCCTAGCTGC | 23072 |
rs183737405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43215355 | CCCTGTCCTAACATG[A/G]TTCAGCATGGCTGAC | 23072 |
rs183758891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156176 | AGACAAATATCTTGT[A/C]CATGAAAGACTACCA | 23072 |
rs183766487 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43187555 | ACTCATTCTAAAATC[A/G]TTTTTGTGACTTCTA | 23072 |
rs183766791 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43387637 | GTTAGACACAGACCA[A/G]TGCTTTTTGTTGGTT | 23072 |
rs183768179 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120547 | ATGTTTGCTGACTGA[C/T]CGAATGATGTAACAG | 23072 |
rs183770271 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43322266 | GGTTTCAGAATGCTA[A/G]CCAGGCTGGTCTCGA | 23072 |
rs183771684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43352459 | TTCTCTGAATTACCT[A/G]GTACATTATTACTGA | 23072 |
rs183774032 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43369897 | ATGATGGAGGGATAG[A/C]TAAATCTGATACAGC | 23072 |
rs183774107 | snp | G/T | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43301245 | GGAAGCTCAGCATGC[G/T]TCTAGTAAAGATACG | 23072 |
rs183780027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43239726 | TGGGGATGTCAGATA[C/T]ACCCACTTAAAATAA | 23072 |
rs183797313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43274853 | AGAAGATATTTACTC[A/G]TGCTAGAAAACAAAC | 23072 |
rs183809349 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43203502 | TGTTGCCCAGGCTGG[A/T]GGGCAGTGGCACAAT | 23072 |
rs183813384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43482086 | TCCACCCTGACTGTT[C/T]GTCACATTTCCAAAC | 23072 |
rs183817009 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43183678 | TTGCCAAATTTCTGA[C/T]TATCCATAGTCAATC | 23072 |
rs183819388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510164 | AGCAGACAAGTCACC[A/G]TGGACGGGCCCAAGA | 23072 |
rs183829523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43549794 | TCTGGCCAGCTGTGG[A/G]AGTGGAAGCTGATGG | 23072 |
rs183843953 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148157 | AAAGGGGAATGAGCC[A/G]AGGGAGAGGTGAGCT | 23072 |
rs183847771 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43272580 | ATGAAGAAATGCTCC[A/G]TGTCACTAATCATCA | 23072 |
rs183854742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256066 | TTAAAGTGTGCTGCT[C/T]ACCATCTCACACACC | 23072 |
rs183866749 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43405548 | CTGTCTACCAGGGAA[C/G]CTTCTTAGAGACTTG | 23072 |
rs183875151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43236875 | TGTAGCTGCCTTATT[C/T]AGGAATAAAATGGGA | 23072 |
rs183881888 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43369314 | AAATACAAAATTTGC[C/T]GGGTGTGGTGGCACA | 23072 |
rs183891105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43187969 | CCCATCAGTGGACTC[C/T]GTGAAGACCCCACTG | 23072 |
rs183891753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43545369 | AGATACAGAAGAACA[A/G]TCCTCTAGTGTAAAG | 23072 |
rs183902396 | snp | C/T | 0.000133983 | 0.00818374 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445332 | CCACACGCGCTTCTC[C/T]TCCGTGGACAGCGCC | 23072 |
rs183904171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116162 | ATCCAGGCCTTCCAC[C/T]ACCCACCCTCAGTAA | 23072 |
rs183905013 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43201600 | GACTTAAGGTACCCA[A/G]GTGGTAAAGCTGACA | 23072 |
rs183909089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43340206 | AGAAAGAAGAAGTCT[A/C]TAATTCCCACCCCCC | 23072 |
rs183909518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43217799 | ACCCACCACTCATGT[C/T]TTTTAGAATTATCAG | 23072 |
rs183927521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298170 | TAGAGTGCACCATTC[A/G]CCCTGTCTGGAATAT | 23072 |
rs183931610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43465367 | ACCTGTCCATCGTGG[G/T]TCAGCTGCGGAGTCG | 23072 |
rs183934712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43448504 | TTTCCTCATGTGCAA[A/G]ATGGGTATAATTACA | 23072 |
rs183935519 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43174072 | TCTTGAACTCCTGGC[C/T]TCAAGCAGTCCTCCC | 23072 |
rs183944895 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43402593 | CCTCACTTTAAAATA[A/G]TATGTAAGCATGTAC | 23072 |
rs183947039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43442077 | GCAAGCCATAGCTCC[C/T]AGTCAGCCATGTGAT | 23072 |
rs183952403 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43423748 | ACATTTAGTGAAATC[A/G]GCCATCGAGGGAGTA | 23072 |
rs183975656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43504458 | CAGCGTAGATTCTGC[A/G]GTTCATCATTTCAAT | 23072 |
rs183977890 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43194789 | CCCTCTGCCTCCTGG[A/G]TTCAAGCAATTCTCC | 23072 |
rs183981349 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43326274 | GCCAACCTTACTGAC[A/G]GTTTGTAATGACTCC | 23072 |
rs183986020 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43307422 | TTCCCATACATACAG[A/T]GATTGGGAGGGCCAC | 23072 |
rs183993436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43259017 | CCTTAGCCCCCAGAT[A/G]TGGGAAAAAGTCAGC | 23072 |
rs183996315 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43382221 | AACCCAGGAGGCGGA[A/G]CTTGCAGTGAGCCGA | 23072 |
rs183997647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43363910 | AGCTCAGTTTGGGTA[G/T]AATCTAGCAACTTTC | 23072 |
rs184002096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43220367 | CGCCTGAGTCTTCAC[A/G]TCCAGAGTTGTTATT | 23072 |
rs184010175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43348811 | ATTTCCATGTATTTG[C/T]ATGGTTTTAAAGGTT | 23072 |
rs184013441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43366182 | ATATACTTGTCAGAC[C/T]CCCTGAGCAGAGGTA | 23072 |
rs184015684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43293621 | ATAATGCGCCATTTC[C/T]TGTAGCTTCAGTCCT | 23072 |
rs184030912 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133537 | TAAATTCAAGTTTTT[C/G]ACCATTTTTCTTTTA | 23072 |
rs184040482 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43439221 | TGGTATTCCTTGTGA[A/T]CTTTTTTATTTCATT | 23072 |
rs184046542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43400066 | ATAACAAGATCCCAT[C/T]GCTACAAAAAGTAAA | 23072 |
rs184052251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377430 | ACCTCACCCTGCCCC[C/G]TCACAATAATTAATC | 23072 |
rs184058569 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43395569 | TTGACAATCTCTTAT[C/G]TGGCCTGGTGCCGAG | 23072 |
rs184060411 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522991 | CTCTTTCCAAAGGTA[A/G]TTCTGCTTGTTTGTT | 23072 |
rs184063467 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43255704 | TGCACTGTGCCAGGT[A/G]CAGGAGATGACATGA | 23072 |
rs184079154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43323697 | TAATGGAATGAAAGC[A/G]TATTCAAACTTGGTC | 23072 |
rs184081304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269537 | AGCATATTTGGGTTA[A/G]GAAGACAGTTTCAAT | 23072 |
rs184085510 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43321647 | CAGAAAGGAAATGGA[A/G]TGATCTGTTATTCCG | 23072 |
rs184094125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300172 | CCTAAATCACTACAG[A/C]TAGGCCTATTCTATA | 23072 |
rs184098124 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43275710 | TTCTTATGCGCACGC[A/G]CACACACACACACAC | 23072 |
rs184104839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43454806 | AATGAAACTGTTAGT[A/G]TCTGACCTACTCCCG | 23072 |
rs184106622 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43360787 | GGCTTGCTCGTGGGG[A/G]AATTATGTTGCAGTT | 23072 |
rs184106762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43232660 | AAGAGGGATGGTGAA[A/G]CTCATGATACCTCTT | 23072 |
rs184113979 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43251660 | ATTCACAGGTCTAAA[C/T]AGCTAAGATGCTTTT | 23072 |
rs184114154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43340629 | AATGCATTTTTTGAT[G/T]GTTTTTGAATTTAGA | 23072 |
rs184125045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43185126 | TGTAGTGAAGTTTCC[A/G]TTAAAAACCCAAAAG | 23072 |
rs184130440 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131213 | GAGGTTGCGGTGAGC[C/G]GAGATCTTGCCACTG | 23072 |
rs184134487 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563805 | ACCTGAGAAGCAGAG[G/T]TTGCAGTGAGCCAAG | 23072 |
rs184135957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130295 | TATACACAATGAGGT[A/G]TCTTGAGGCTGGAAC | 23072 |
rs184136779 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198951 | GAAGGCTCTCACAGC[A/G]TGCTTCCTACCTTGT | 23072 |
rs184138363 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43212982 | GAAGTATATTTAAAG[A/C]ATGAGCTAAGATTAA | 23072 |
rs184153253 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43486581 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 23072 |
rs184158658 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114132 | TGCAATTCTCCCCTT[G/T]TTTTCCCCCCTTCTC | 23072 |
rs184159479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380054 | TTGGTGGCCTTGGGC[C/T]TCAATTTCTCTTTTG | 23072 |
rs184159632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43315423 | GCCTAGTAGTAAGAA[A/G]GACAAGTAGATTCTC | 23072 |
rs184164380 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43344050 | GTTGGCTGCATAAAT[A/G]TCTTCTTTTGAGAAG | 23072 |
rs184166833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519958 | TCACAGGAGATGAGC[C/T]GAGGTAACAGGAGCC | 23072 |
rs184177000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420042 | GAGAAAGGTAAAAAC[A/C]CCTTCAAATAAGGAA | 23072 |
rs184177150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43460833 | ACTGCCTCTGTGCTT[C/T]GGCAGAGGTCAGACG | 23072 |
rs184187184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43446214 | GGAAAAATAACATGA[C/T]TGTGTATAAATGACT | 23072 |
rs184196949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43483924 | GAGCTATTCGAGAGA[A/G]GCCTGCTAGAGACCA | 23072 |
rs184203724 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520504 | TCTTCTCTCATTTAC[A/G/T]TGGGCGCAAATTTCC | 23072 |
rs184206867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43501384 | TTTCCTCCAGTGAAG[A/G]TGAATGAAAGGCAAC | 23072 |
rs184218214 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43541810 | TATAACCACATTTTG[A/C]AGTGAGGTCTGGGCA | 23072 |
rs184230141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43271541 | CAATGGACAAAAATC[A/G]GTAGCATTTCTATAC | 23072 |
rs184240629 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378672 | TTAGCTGAGTGTGGT[A/G]GTGTGCACCTGTAAT | 23072 |
rs184251842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427534 | TCTATTATGCTGTTA[C/T]TTGCCCTAATTTAGA | 23072 |
rs184252690 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115007 | AACAAAAGAAATATT[A/G]AAAGGCCAGATGTGA | 23072 |
rs184262797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43417860 | TTTCAAGTTGGATTT[C/T]GGCATTCCCAGGCAT | 23072 |
rs184265943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146712 | AATAGAGGATGTATG[A/C]TGGACAAGGCTTCTT | 23072 |
rs184266183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43453483 | TCCAACACTTGGTTT[C/T]GATCATCCTGTGTTT | 23072 |
rs184268616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43392015 | TGCAAAGTGGAACTC[A/G]TAATTCCCTACTTTC | 23072 |
rs184294526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43316013 | ACAGCAATAGCATGT[C/T]TGTTGTCCACTCTTC | 23072 |
rs184298455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43295163 | AAAAATCAGGTATGC[A/G]TTGTCTCGTGTGAGC | 23072 |
rs184305137 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43273223 | AATTGCTGGGTACAA[C/T]GCTCAGTACCTGGTT | 23072 |
rs184313564 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43358071 | TAATTTTTTCTTTAA[A/G]TGGAAATCTAGTAGT | 23072 |
rs184317502 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43373176 | TGGTGCTGCCCATGC[A/T]CGTTGGTGTCGTTCT | 23072 |
rs184317990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43309948 | TAAGAACTTGACTTG[A/C]ATTGTCTCATTAAAT | 23072 |
rs184332596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43337003 | AGTGCTGCAATAAAC[A/G]TAGGAGTGCAGATGT | 23072 |
rs184338277 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43342916 | CTGTAGTCCCAGCTA[C/G]TCAGGAGGCTGAGGC | 23072 |
rs184350258 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43232077 | TGATCCCAGAGTTGA[C/T]AGTAATTGGAGAAAA | 23072 |
rs184353937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125478 | GAGTGAGGCATTGGT[C/T]GGGTGTGGTGGCTCA | 23072 |
rs184364740 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43397500 | TGCAGGTGGGCTGAG[C/T]ACGAAAAGAGAGTCA | 23072 |
rs184378547 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43361970 | AACATGGTGAAACGC[C/T]GTCTCTACTAAAAAT | 23072 |
rs184382056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268982 | AGATGGGGTCTTGGT[A/G]TGTTGCCTAGGCTTA | 23072 |
rs184383821 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198797 | CCACACTCACGTGCA[C/G]ACACACATCCTCGCA | 23072 |
rs184394059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43437106 | CCTACCAGCCCACTT[A/C]CTGGACTTCAGTTTG | 23072 |
rs184401771 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43460558 | TGTGTGTGCGTGTGT[G/T]CGTGTGTGTGTGTGT | 23072 |
rs184411039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43479373 | CTGATCTGACAGGAG[A/G]TGGAGCTCAAGTGGT | 23072 |
rs184413780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43500516 | GCAAGTCTGTAGAAA[A/C]GCCATCCCTCATAGA | 23072 |
rs184418696 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43547919 | AAAGATCACTTTTTA[A/C]TGTGATACACAGTTT | 23072 |
rs184422885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43497436 | TTTCAGCTGGAAAGA[A/C]ATATGATTGCATCTG | 23072 |
rs184424517 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517206 | CAAAATGTCTGTGAG[A/C]TCATTTATGTCTGTG | 23072 |
rs184429528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43536073 | GCTCTTCATCTGAAG[A/G]AAAACAGAGCATGCT | 23072 |
rs184445669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43287585 | TAGAGTGATCCTCCT[A/G]CCTCAGCCTCCCAAT | 23072 |
rs184467955 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43534601 | ATTTGAGCAATTAAC[C/G]TAGTCAAACAGGGTT | 23072 |
rs184471378 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43436076 | GGTTGAGGCAGGAGA[A/G]TGGCGTGAACCTGGG | 23072 |
rs184478936 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43471310 | TGAGAGTTAGGAATA[C/T]AACTCACTAAACAGT | 23072 |
rs184483938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43453247 | AACCCAGGTGACAAA[A/C]AATAGTAGCTTGGGC | 23072 |
rs184484622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43251265 | TTGCCTAGCCTAGTG[A/G]GACAGGGGACTGAAT | 23072 |
rs184492062 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43491491 | AAAGTTATAGGCGTA[A/C]CTTACCAATGATATT | 23072 |
rs184514459 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43211871 | AGAAGGGGATGCTTT[G/T]TCCTGCATGTTTGTG | 23072 |
rs184536935 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43456734 | GGCCAGTGTATGCCC[C/T]TCTCCTGCGATGTTC | 23072 |
rs184537182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43496654 | CCCAAGAGCAGATGG[C/T]GACCCCTGTTCAGCC | 23072 |
rs184541532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43396281 | GTGTTCTGAAATTTC[C/T]GAGGAAGGCAATTGA | 23072 |
rs184544113 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43184653 | CGGGCTAAAGGTTGA[A/G]TTGATCACCAATGGC | 23072 |
rs184551164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43417477 | TTTATTTGAATGTCT[C/T]TATTTAATGTCCTGC | 23072 |
rs184555489 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43378451 | GCTCTCTCAGATAAC[C/G]TGCCTTAGAAAGATT | 23072 |
rs184559391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207545 | GTTAATTGTAGTCAT[C/T]TTACCATGCTATAGA | 23072 |
rs184569784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43356570 | CTATAGAACATTTCA[C/T]TCAACTGCTGCAGAA | 23072 |
rs184570387 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | HECW1 | GRCh38.p7 | 7:43226909 | ACAGGATGGGGGCCA[C/T]CTCCAGCCGTCCAAA | 23072 |
rs184577993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161138 | TGTGTGTCATGACTG[A/G]TTGGGAATGAAGGAT | 23072 |
rs184580644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516421 | TTTAAACTAAAATAA[A/G]ATAAATAAAAACAGT | 23072 |
rs184585728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43391752 | TCATATAATGAGGGT[A/C]TAATGAGGGAAATGC | 23072 |
rs184587259 | snp | A/T | 0.0543475 | 0.155628 | intron-variant | HECW1 | GRCh38.p7 | 7:43181999 | CCATGTTAGCCAGGA[A/T]GGTCTCGATCTCCTG | 23072 |
rs184591080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43430053 | AAATTAACTTTCCTT[A/C]CCAGTTTTCCATCCT | 23072 |
rs184592546 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124955 | ATGCCTTAGTTTGGG[A/G]TGTTATACCAAATAC | 23072 |
rs184593611 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166706 | GTATAATAGGAACCT[G/T]TGTCCACTAAAGAGT | 23072 |
rs184600301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43558508 | TGCCCCTCTTCCCCC[A/G]CAAGAGGCAGTTGAC | 23072 |
rs184603716 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43246086 | GGAGGATCACTTGAC[A/G]CCACGAGTATGAGAC | 23072 |
rs184603999 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43195396 | CATCTCCTGGGGGCC[A/C]GGCCCTGGGCAAGGC | 23072 |
rs184606297 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130881 | TATTAATAACTGGGT[A/G]TACAATAATCTACTT | 23072 |
rs184621677 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146337 | CCCACCCTACCCTCT[C/T]CAGTTGTAACAATCA | 23072 |
rs184628366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43281846 | GATTTAATATTATGG[A/G]TGTGAGCCACCATGC | 23072 |
rs184633132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43315556 | TAGAGTACAATGGCA[C/T]GATCCCAGCTCACTG | 23072 |
rs184651868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43542417 | TTATGTAGATATATA[A/T]GTATATGCACATATA | 23072 |
rs184661891 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43564117 | GATTCCAATGGAGCT[A/G]TTGTTTTATTTATGA | 23072 |
rs184662248 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43478007 | GGTACAAAGGGTTTT[G/T]TTGAAAAAAAAGGTA | 23072 |
rs184683750 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43372332 | CTTTTTTACCTGTTT[A/G]TATTTACTAACAAAG | 23072 |
rs184694237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157041 | TGACACATGTTCATT[C/T]GCAAACCTGGGCTTT | 23072 |
rs184703538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43336251 | ATCATACCTCACTGC[A/G]GCCTCAAGGGCTCAA | 23072 |
rs184713530 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121378 | GGAGTGGCCAAAGTA[C/T]GCACAATTCCCTAGG | 23072 |
rs184716478 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43431222 | TCCTGCACTTATACC[A/G]TAGAACTTGTTGAAA | 23072 |
rs184726179 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43553635 | GATCATGCCACTGCA[C/T]TCCAGCCTGGGCAAC | 23072 |
rs184726733 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43467444 | GCAGGAGGGAGAGGG[G/T]AGGAGGGGCTTGAGA | 23072 |
rs184728139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515476 | CAGAAGCAGTAGAAA[C/T]GGAAAGATTTTTCAG | 23072 |
rs184728378 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43496145 | ATTTTGCAGAGCTGG[A/G]GGAACTTGAAATCAG | 23072 |
rs184729856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43449335 | CCTTCCTTGTTTTCC[A/G]TTAGCATCTCCAAGG | 23072 |
rs184730133 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43409697 | TGCCTCATCTCATGT[C/T]CCCCTGGTAAGGCTC | 23072 |
rs184739058 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43488385 | GGAAGGAAGGAAGGA[A/G]GGAAGGAAGGAAGGA | 23072 |
rs184740034 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43534020 | TCCTTAGCAGCCCAA[C/G]TTTAATGCCGGGAAA | 23072 |
rs184745537 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43557734 | CAAGCTTCTTAAACC[A/G]TAGTCCACAGAAAGA | 23072 |
rs184761548 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358668 | ACAAAAATAATAATC[A/G]GATTCTATTTTAAGC | 23072 |
rs184768537 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43286204 | GAACAGAGAGATGAT[A/G]AGAAATCAGCACAGT | 23072 |
rs184772465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268278 | GAAGGAGACTCGCAG[C/T]GTTCTGTAACAGTGT | 23072 |
rs184775090 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43411374 | CAATCTATTTAAATT[G/T]ATCAAGCCATGTTTT | 23072 |
rs184776860 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43264792 | GAGCTTGCAGTGAGC[C/G]GAGATCGCACCACTG | 23072 |
rs184778625 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43374383 | TTTGACCAACAGTCA[C/T]AGGTATGTGACTTAG | 23072 |
rs184786414 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43294135 | GGCAAACTCTCATGT[A/G]CATTGCAGTGGAAAC | 23072 |
rs184786964 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43392575 | TGTTCCCAGGCAGGC[A/T]CCCTTGCCCTTGGGC | 23072 |
rs184788003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43250610 | TCCTGTGTGTACCTG[C/T]CCTGCCTTGTACTTC | 23072 |
rs184789775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43204604 | ACACAAAGCTGAACA[C/T]TAGTTAAGGAGACAA | 23072 |
rs184794122 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43228929 | GACAACGAGGAATCT[A/G]CCAAATTGGTTAACA | 23072 |
rs184794489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222922 | TGACATACATTTTCA[C/T]TTCCATCCCACATCT | 23072 |
rs184817588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43179667 | TACAAAGAAGTGTTT[A/T]AAATATATTTAGTAT | 23072 |
rs184820288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138698 | CCCTCTCTCTCTTTT[A/G]GACCAAGTGACCTAA | 23072 |
rs184822897 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43211126 | GCTCTCTCATTAGTC[A/C/G/T]GGTGTGAGCTAAGTT | 23072 |
rs184825533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162741 | GCCTTTTAATACAGA[A/G]GTAGTGGTCCCTATA | 23072 |
rs184827493 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43370165 | AGTCAACAATGAGAA[A/G]GCAATCAAGCCAACT | 23072 |
rs184829885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43192120 | ATCTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 23072 |
rs184833178 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43231752 | CCAGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 23072 |
rs184842226 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126350 | CACATATATATCATT[A/G]TCTAAAGCAAGGGTC | 23072 |
rs184846058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530243 | GATTACAGGCATGAG[A/C]CACCATGCCTGGCTC | 23072 |
rs184859083 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43187644 | CTTTTCCTTTATATT[A/G]TAATTTTCTTTTCTA | 23072 |
rs184862137 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143938 | CAAGATTTGACCTGC[C/T]AAGACTGTGTTTGTC | 23072 |
rs184872176 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43407799 | TGTGAACCAGCCCTC[C/G]TCCTTCCCTCCATTC | 23072 |
rs184905239 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43331362 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACAAGGT | 23072 |
rs184917559 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43288561 | AGGCCCCGCTCTCCA[C/T]TCACTCATCCTGTGG | 23072 |
rs184930349 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43222345 | TTCCATCTCTGTATT[C/T]TGCACATCTTTCAAA | 23072 |
rs184934002 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43446942 | GGCGCAGGAAGATGG[A/G]GTGGCATCAGGTGAT | 23072 |
rs184939282 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43417024 | CTGTAGACCGGAGCT[C/G]TTCCTATTCGGCCAT | 23072 |
rs184940383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428715 | GGCAAAGTTAGAATA[A/G]TAGCTCTTTTCTTCC | 23072 |
rs184943484 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43388603 | ATACTGTTTCTCAGC[C/T]CCAGGGTGTTACTGC | 23072 |
rs184948491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43463269 | TAGAACTGCTAGCCC[A/G]GTTTGTACACTTATT | 23072 |
rs184951898 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260386 | TCACGTGGAAAGACC[A/G]AAAAGTGGCAAGATA | 23072 |
rs184957284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43353121 | GCTCTACTTCGTGAA[A/G]GACATGGTCACCCCG | 23072 |
rs184968306 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43191397 | TGCTTTCTAATTACA[C/T]TTCTTGGACAAAACA | 23072 |
rs184975216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43559164 | GAAAAATAGAGGAGA[C/T]GGGGAGATCAACTGT | 23072 |
rs184986238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161682 | TTGGAGAGGTGATGA[C/T]GGTTTCCATTATTTT | 23072 |
rs185012147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43408606 | TGGGAGGACTTCTTG[A/G]GCCTGACAGGCAGAG | 23072 |
rs185015823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43281362 | ACAATAGCTGACATT[C/G]GGTGGACACCTGCTG | 23072 |
rs185017217 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43311146 | ATACAGTCCTCTGAG[A/T]TTGGATTTTATTGAA | 23072 |
rs185022513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43370684 | CTAAAAAAAAATGAG[C/G]TGCCAAGCTATAAAA | 23072 |
rs185030832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43389908 | AAAGCGCTGAGATTA[C/T]AGGTGTGAGCCACCC | 23072 |
rs185031895 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43488245 | AACCCGGGAGGCAGA[G/T]GTTGCAGTGAGCCAA | 23072 |
rs185037796 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43244662 | TGGCTGCTCTGAAGT[C/G]TCCCAGTGGGTAACT | 23072 |
rs185038158 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524106 | ATAACCCACCCCATA[A/C/G]AGTCTGATCTCCAGG | 23072 |
rs185048255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43240457 | TATCAGACGACAGAC[A/C]GAATGAAAGAGGAGG | 23072 |
rs185056071 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43325552 | GAACTGGGCAGTGTG[C/T]CTGGACTGACCTCTG | 23072 |
rs185056307 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43306707 | TCACTCACGGCTTTA[C/T]ATTCCAAGACAGAAA | 23072 |
rs185070283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43179138 | TCAAAGTTGTTGACA[C/G]TCAAAAGGCACAGGT | 23072 |
rs185074631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43410280 | CGGTTGGGTTCTGGT[G/T]AGGGCCTCTTTGGGG | 23072 |
rs185075056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43208359 | GTTACTGTCTTATGA[C/T]TCCCACATCTTCCTT | 23072 |
rs185077845 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43203910 | TCTTGCTATTATGTA[A/G]TATCTTGTATTCACT | 23072 |
rs185079274 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43228258 | TGGGAGGCCAAGGCA[A/G]GGGAATCACTTGAGT | 23072 |
rs185087231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143277 | TGCCCGGCCAAGGCC[A/G]CCTTTCTTTTTTATA | 23072 |
rs185100278 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43449078 | TGTATTTCCACTAGC[G/T]TGGAGGAGTAATTAA | 23072 |
rs185122321 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43346341 | CACTTTTTGATGGGA[C/T]TGTTTGTTTTTTTCT | 23072 |
rs185122597 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513718 | TTGGTCAGGATTTTT[G/T]ATTTTTGTTTTGTTT | 23072 |
rs185122665 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494813 | GCCACCTCACCCAGC[C/T]TAAAGTCAAGATTTC | 23072 |
rs185134086 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43505746 | GCAATCTAATTTGTG[C/T]CTATTTATTCTTTAG | 23072 |
rs185135572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43531333 | TGCACTTCTCTTCAC[C/G]ACTTGCTCTGTGGTG | 23072 |
rs185139458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43555221 | TATTTGTGGTGTGTC[A/G]GATTTTTCCTATCAA | 23072 |
rs185177110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43443962 | AGGCTTTGGGCATTT[A/T]AACCAAAAGATGAAT | 23072 |
rs185179209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43488732 | TTCCTGGGCCCCTTG[G/T]TGGAGAAGGGCGTTT | 23072 |
rs185179607 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43468430 | TGGAGTCGCACAGAG[A/G]GGTGGGCCGTGTCCC | 23072 |
rs185181836 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43237106 | AGGGATGGGAGGGAG[C/G]GAAGAAAGAAAAAAA | 23072 |
rs185185567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43507789 | CTTAAAAGTAGTTCC[A/G]TATGATGGAATGCAC | 23072 |
rs185192076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43458863 | TATTATTCAGTGTTG[C/G]AAGGAGTTTCCCTTG | 23072 |
rs185196488 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43430855 | GGGGTGATCTCGGCT[A/C]ACCACAACCTCTGCC | 23072 |
rs185199245 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43525300 | TAATTTCCATGAAAT[A/C]AGTTCATTTCCTGAA | 23072 |
rs185200966 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43305918 | GGCATGTGCCACCAC[A/G]CCTGGCTAATTTTGT | 23072 |
rs185203105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43175329 | TTGTTATAGCTACAG[C/T]CACCATGTTGTACAA | 23072 |
rs185203464 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43548402 | TCCAAACCCACGCTG[C/G]TCAAGGGTCAGCCTG | 23072 |
rs185214542 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264549 | TGTCTTTTGTAAAAA[A/G]TAATTACTATTGTCA | 23072 |
rs185217820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43202292 | TCAAGATCTGTACTC[C/T]GTAGGATCTCTCTCT | 23072 |
rs185221648 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139281 | GGGGAGCACCATGGC[A/C]AACCTCAGCCTGGGC | 23072 |
rs185222758 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43350243 | ATCTGCTGTCAATCT[G/T]ATACGTTTTCCTTTA | 23072 |
rs185227000 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43368337 | TGAAATGTGCACACA[C/G]CACAGCCATGATTTC | 23072 |
rs185233410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43466227 | TTGTGATAAAAGGGA[A/G]GAGATGTTGGAGGAC | 23072 |
rs185241109 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43364911 | ATTACAGTCTTCTTA[A/T]ATAAGCCCCATGATA | 23072 |
rs185244040 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43327597 | CTCTGGTTATACCTC[A/G/T]TACTCATGTTGGTCT | 23072 |
rs185247375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43324803 | GGGATTAAATTAACA[C/T]AATAAAATAAAATGA | 23072 |
rs185249109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43404697 | AAAAGCACAGACTTT[A/G]GGCCGGGCACAGTGG | 23072 |
rs185254532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114531 | AGAATTCCCTGTTGG[C/T]AGAATTCCCTGTTGC | 23072 |
rs185257044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424971 | ACATTATATATTAGG[C/G]AGGGAATAATGGGTA | 23072 |
rs185264203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43385074 | GAGTTTCATAATTTG[C/T]AAGAAAAAGATCCTG | 23072 |
rs185269546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43502099 | TTGCATTCCAAAGTC[A/G]CTCTCCGAGCATTTC | 23072 |
rs185270599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43277542 | CATGACTGGGACCCA[C/T]CTGCACACCAGGCCT | 23072 |
rs185273042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529353 | CCCATCTGAAGGACA[A/G]AACGCCACTGTGGAT | 23072 |
rs185279259 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43261848 | TTTTTGCTTTGTTTT[G/T]TTTTTTATTTTTTAT | 23072 |
rs185290466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43218942 | ACAGAGAGAGCAGTG[C/T]CGGGGAGCCAAGAGA | 23072 |
rs185316361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43188686 | TAAAAATTAAATGTA[C/T]TGGCTGGAAATGACA | 23072 |
rs185320619 | snp | A/C/G | 0.00319074 | 0.0398324 | intron-variant | HECW1 | GRCh38.p7 | 7:43280637 | GGAGGATGAGTACTC[A/C/G]TGATAATCCCAGTAC | 23072 |
rs185321534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43205488 | CCTGTAGTGGGGTGG[A/G]TGAAATCACTTGTGC | 23072 |
rs185323696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43171333 | GATGGTTAAGATTTC[A/G]TGTGCTGCTTTTATA | 23072 |
rs185325548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43223356 | GGCGCCATGGCTCAC[G/T]CCTGTAATCCCAACA | 23072 |
rs185329169 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43185940 | TCACAAGGCAGTGTC[A/G]GCTGGCTCCAGCAAG | 23072 |
rs185332265 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43428078 | AGAGTGTGTACACAG[C/G]GGGCAGGAATCTTGA | 23072 |
rs185332466 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43244169 | TGTGGAGTCCTCCTT[C/G]TGTGATGTGAACGTA | 23072 |
rs185333017 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43199768 | CTTACTGAGTAGGAA[A/G]GGGCTTTTATTTCTC | 23072 |
rs185335413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242292 | CTCCATGGGAGTTGA[G/T]TGGGAGAGGGAGGTT | 23072 |
rs185340003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136537 | GAGCTGGCAAAAACG[A/G]GTCACTTCTGGAAGC | 23072 |
rs185345878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119473 | TTTGACCTTTAAATG[C/T]GGGTACGGGGATTCC | 23072 |
rs185352500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154568 | TTGTTCTTCTTTACA[C/T]CTTAGGTGTATTTGT | 23072 |
rs185357545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157710 | GTACTATAGGCACAT[A/G]CCACCAAACCTGGCT | 23072 |
rs185358866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192586 | TAAATTCAATTAAAT[A/C]TCCTAATTATATTAA | 23072 |
rs185366684 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43461938 | ACTTCCTAAAGAACT[C/T]GTTAGAAATGCAGAT | 23072 |
rs185374567 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43361459 | ATAGGCCTGGAAAGA[A/C]CAGAATCTCTCACCC | 23072 |
rs185379225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147565 | TGCTTACATCTATTT[A/G]TGGACTTTTTTGTAT | 23072 |
rs185387408 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43168216 | TATGAGTGTTGAATC[A/G]TGGGATGCTATCTTA | 23072 |
rs185390440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43322155 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 23072 |
rs185394059 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115521 | TATGCAGTAATTGAC[A/G]ATGGCATGAGACTTA | 23072 |
rs185397015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43551866 | GTAAGGGGCCACCTT[C/G]TGGTTCATAGATGGT | 23072 |
rs185399067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520853 | TAATCTACTGTCTGC[A/G]TCTCTCCTTCCATCC | 23072 |
rs185412126 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132039 | GTTGTTAGGTTCAGA[C/T]GCAAAGGCAAATGCA | 23072 |
rs185422463 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43485869 | CACTAAATTTTTTTT[A/G]TTATTATACTTTAAG | 23072 |
rs185438599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43408102 | TCCTTGAGCAAGGGT[A/G]TCAAATCTTAAATAT | 23072 |
rs185444869 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43503815 | TCATGGGGACAGGTG[A/T]TAGTACCAGCGGTAG | 23072 |
rs185446257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43276666 | AAATGCTTTAGGCCA[A/G]TGCAGTCTTCCCTGT | 23072 |
rs185447241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123442 | CTGTAGGAACATGCT[C/T]TCCTGTGACCCTGCG | 23072 |
rs185451186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522030 | GCCATTTGAGGATAC[C/T]GCAAGGTGTCCATCT | 23072 |
rs185452664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43241354 | CTCTTTGGTGGGGTG[A/G]GGTAAGCTTCCAGGA | 23072 |
rs185453284 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43544330 | CAACCTAATAGAAAA[A/G]TCACAAAGAATATAG | 23072 |
rs185470022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43446690 | TATTCAATAATGCCC[A/G]CTTCTACATTTCAGA | 23072 |
rs185475865 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511890 | CACAAAATGCTGGCA[A/G]TGTGTGGGTGCTGTG | 23072 |
rs185477790 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43484240 | CCACGTCTTCAGGAC[A/C]GCATAACTAAGAGAC | 23072 |
rs185492511 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150280 | GAAAGCTTTTAGTTA[C/T]GCTGTCTATAACACT | 23072 |
rs185496991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43341373 | TGTCATTTTACATAT[C/T]GGTTCGTTTTGGTCA | 23072 |
rs185506397 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43184368 | CAGTGTGATGCTACC[A/G]AACACTGAGTTGGGC | 23072 |
rs185507946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296424 | TGCCCAGGAAGGTCT[A/G]TGGTGTGTCCTCCTA | 23072 |
rs185509615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118048 | GGATGGAACTTAAGC[C/T]GGTACCAGGGGGGCG | 23072 |
rs185512708 | snp | A/G | 0.000629181 | 0.0177255 | missense | HECW1 | GRCh38.p7 | 7:43463727 | GGCAGCCAAAGCTGC[A/G]AGCAAGCCCCAGCAG | 23072 |
rs185516094 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43548162 | TTAACTTTTTAATAA[C/T]AGATTTGTGTACATT | 23072 |
rs185517002 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43447340 | TTTACAAACAAAAAA[C/G]TCACATCCTTGCCCT | 23072 |
rs185518846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43274040 | ATTTTTAGTGGAGAC[A/G]GGGTTTTGCCATGTT | 23072 |
rs185526698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257863 | AAGAAGAAGAATAGT[G/T]GTATTCAGTGGGATA | 23072 |
rs185557357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203136 | GACTTCCCAAAGTGC[C/T]GGGATTACAAGGGTG | 23072 |
rs185558381 | snp | A/G/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43477785 | CTCTTTAAACTGCTT[A/G/T]TTTACAGTGACATCA | 23072 |
rs185563560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300574 | TTTATATTGCTAACG[A/G]CCATGCCTGCTTCAC | 23072 |
rs185572736 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43219678 | ACAGGACAGGGATTT[G/T]CACAGTGCTTTTCTA | 23072 |
rs185578677 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43238231 | CAATAAAGCGCTGCA[C/T]TGGGAGGGATGGCAC | 23072 |
rs185584888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43261202 | GATAAGAGAAGTTAT[A/G]GCTAGTGATGAATAT | 23072 |
rs185593148 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198379 | CGCTCTCACACACAC[A/G]TCTTACACACACTCA | 23072 |
rs185599740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43506931 | AAAAATCAGCCAGGT[A/G]TGGTGGCACACACCT | 23072 |
rs185611352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43401653 | CAAAAGAACAATCCT[C/T]ATGCTAATCTCAGAC | 23072 |
rs185616234 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43365827 | GGCTGGGTGCAGTGG[C/T]TCACGCCTGTAATCC | 23072 |
rs185616915 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43169999 | CAGAACCGCTGGACA[A/G]ATCATTTAATGCAGG | 23072 |
rs185629825 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145095 | TACAACTTTATTCCC[A/G]AAATAAATTACTAAC | 23072 |
rs185647064 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43382964 | AGGCCCCAGTGTGTG[A/G]TGTTCCCTTCCCTGT | 23072 |
rs185647952 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111574 | GCCTTCACATCGTCC[A/G]AAGTTTCCAGTTCTG | 23072 |
rs185648195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152174 | TGTGAAAATACTTAG[C/G]AAATATTCTGTTAAT | 23072 |
rs185649726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43440782 | TAAACAGACAAAATA[C/T]TGAAGCTCATCCTAT | 23072 |
rs185658514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43170580 | GGGACAGCACACTCT[A/C]ACTGGCAGAGGTCAG | 23072 |
rs185659172 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134597 | TGCAGCTTTGAACTC[C/T]TGGGCTCAAGCAATC | 23072 |
rs185665043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127933 | ACTCAGACTGGCATG[A/T]AGTAGCATGATCACA | 23072 |
rs185707996 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43196333 | TTTAATATATAAAAA[G/T]GTAGGCACTGCCTCT | 23072 |
rs185723535 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43418951 | GACAATTGATTTGGC[A/G]CAGCTCCTACTGTCA | 23072 |
rs185730924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43167307 | CCCTATGTCTCTGTG[A/T]CTTCTCTTCTATTCG | 23072 |
rs185733868 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43524772 | GTTTGGGGCTATTGT[A/T]TCACCTCTAGCTCTC | 23072 |
rs185740186 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43381724 | AGACAGAGTTTCACC[A/G]TGTTGGCTAGGCTGG | 23072 |
rs185749350 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43216434 | CAGGTGTGTGCCACC[A/G]CATGCCAGCCGAAGC | 23072 |
rs185754751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43343231 | TGTTCAGATATTCAC[A/G]GTGCTGGCAAACTGC | 23072 |
rs185754903 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43293199 | CGCTCCAGCCTGGGC[A/G]ACACAGCGAGACTAT | 23072 |
rs185759076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43322911 | CAGTAAAGTAGCAGT[C/T]CTCAATGGTGCTGGC | 23072 |
rs185763171 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43271160 | ATCTAGAAGACTGAG[C/T]GGAAAACTTAACCAA | 23072 |
rs185772182 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302504 | TGGTGCCCTGGTTAC[A/G]GGAAGAGGCACAGTG | 23072 |
rs185774912 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43455722 | CATCACGGGTGTGAT[C/G]ACCCGTGCCTGTAAT | 23072 |
rs185778913 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43422860 | TAAGCTAAAAGCCCT[A/G]TCACCTGGAGATAAA | 23072 |
rs185783772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43398744 | CACAGAACTGTCTGT[A/G]CAGGAGACCAGAGTT | 23072 |
rs185796371 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43362838 | TGCCAACACACAGCA[C/G]TTCACTGAATGAGGC | 23072 |
rs185809862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420133 | TTAGGCTAAATTGTG[G/T]GAGCTAAGAACATAA | 23072 |
rs185821805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43347331 | TCTCTGCTTGGTTGC[C/T]GTTGATGTATAGAAG | 23072 |
rs185841483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43485228 | TGCAGTGAGCTTCTT[C/T]GATGGCAGAAGTCAT | 23072 |
rs185845115 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43229853 | CTTAACCAAGAGTTG[C/G]CATCATCAGTGCAGC | 23072 |
rs185851924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521305 | CAGTAGCACCACCAC[A/G]ATCACCCCCAGCTGT | 23072 |
rs185853575 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43246463 | CAACCAGGGGTACAT[C/G/T]GCAAACCACCAAGTC | 23072 |
rs185869577 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43201468 | GAATCCACGCTCAAT[A/G]GGATGCTAGGGGGCT | 23072 |
rs185870915 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43183528 | AAGAAGAATATATAT[A/C]CACATACACTTATTT | 23072 |
rs185874949 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43196826 | CATATGAAGAATAAT[G/T]TGTAATATTTTACAT | 23072 |
rs185884162 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43182392 | CCAGTTTTCCCAGCC[C/G]CATTTACTGAAAAGA | 23072 |
rs185887390 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43543503 | GCTACTCATGGCTGG[C/G]CACGGTGGCTCACGC | 23072 |
rs185889109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43209560 | AAGAGATTAGAATTT[C/G]CAAGAAAGAGCCTCC | 23072 |
rs185893071 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147763 | GGAGAGTTTCAGCTG[A/C]GAAGGGACTGGCCAT | 23072 |
rs185914733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43168793 | AAGTCAATAAGTATA[C/T]GCAAGGATACTCAGT | 23072 |
rs185934437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43312414 | TTTTAAGTCTATGTG[C/T]TTATAAGACAAAGTA | 23072 |
rs185947663 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43271077 | AAAAATGTCAAGGAG[A/T]TAGATTTATATAATT | 23072 |
rs185951972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43457511 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 23072 |
rs185955128 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43400067 | TAACAAGATCCCATT[C/G]CTACAAAAAGTAAAA | 23072 |
rs185965698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412196 | TTAATTTTGTACCAC[C/T]TTACATAAAATGCAG | 23072 |
rs185971053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43439370 | AATTCAGACTCACAC[C/T]TGTGTCTCTCCAAAG | 23072 |
rs185980801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43474428 | CACTCCAGCCTGAGC[A/G]ACAGAGCGAGACTCT | 23072 |
rs185997692 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43332634 | CACAGCAGATGGGAG[A/C]AAAGGCGGCTGCGGT | 23072 |
rs185997855 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43339774 | TGCAGTCCAATTCTG[A/G]TAAGCCACAGTCTCC | 23072 |
rs186000419 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180174 | TCACCAACTTATAGC[A/C]GAGGTTATGTGACTG | 23072 |
rs186011184 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43537883 | ACCTTATGGTCTTCC[C/T]AATTCAAAGCAAATA | 23072 |
rs186013188 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111090 | CATCTCTGAGCCAAG[C/T]TGATGCTGATTCACT | 23072 |
rs186017414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144550 | AGTATGAACTCAGGA[G/T]TATTTTTTTATTATT | 23072 |
rs186021101 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296950 | CTTTTTGTGACAACC[A/G]CCAATTAGAGACAGT | 23072 |
rs186023310 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43424230 | AATTACTATGCTCCA[C/G]TGACAAATCTCAAGT | 23072 |
rs186024536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375662 | GTTTGGGAGGCTGAA[A/G]TGGGCAGATCACTTG | 23072 |
rs186028443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43393907 | TTTTAAAAAATATAC[A/T]TTGGAATGCACATAC | 23072 |
rs186034589 | snp | A/G | 0.0128194 | 0.0790277 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43442589 | TCATGTGAGTGGACA[A/G]CTGCAATTCCGATTT | 23072 |
rs186036648 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359199 | CCTTTACATATCAGT[A/T]AGGTTTATGTTTAGC | 23072 |
rs186062076 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214536 | AATTTAGATGGCAAC[A/G/T]CTACTTTCCCCTGCC | 23072 |
rs186064841 | snp | A/G | 0.000399281 | 0.0141238 | missense | HECW1 | GRCh38.p7 | 7:43312057 | AAGGAGGAAGTGGAC[A/G]CTGGGGACTGGATTG | 23072 |
rs186065997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43291373 | AACTTTTTTTAAATA[A/G]GTAAAGGCAAGGGAG | 23072 |
rs186074145 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | HECW1 | GRCh38.p7 | 7:43274645 | CCCGGGGGAGGGAGG[A/G]AGAGAGAGAGAGAGA | 23072 |
rs186081953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43498342 | CTGGGCTTCTTTTTC[C/T]CGCAGGGAGGGAGGC | 23072 |
rs186082889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253068 | GGAGCTTGGACATGG[A/C]TTTTCAGCTGCTTGG | 23072 |
rs186087086 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43225145 | TGGACTGAGCCAGAT[C/T]GAGGGACTCACCCAG | 23072 |
rs186093262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43243218 | CTGACAGATGATGCC[A/G]TCAGCAACTGTCCCA | 23072 |
rs186105186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43353473 | ATGGCTTCACTTCCC[A/C]CCACAGAAAATTTAA | 23072 |
rs186107557 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43332260 | ACTCTACATACAAAA[C/T]GAATCTCTTTTGCTC | 23072 |
rs186108735 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43393331 | CTCCAGGGTGAAACT[A/G]TTTGGGCTGAGTCTT | 23072 |
rs186120606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162836 | CTTGTTCTGTGGGAG[A/G]CATTGTTCTAACTAC | 23072 |
rs186121888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43193852 | TGCCTAACTATGTAC[C/T]CTAACAGAAAGACCT | 23072 |
rs186123824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206379 | GAAGGTAAGGGTTGG[C/T]CAAAAAGGTCTACCG | 23072 |
rs186129609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43252732 | TAAATATAACTAGCA[A/G]TTGGCCAGACTATAA | 23072 |
rs186145869 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43561206 | AGCAAGCTAGAACCC[C/T]GGGCGCCAGGACACT | 23072 |
rs186150838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43181077 | CTTTTTAAGATTCCA[C/T]ATATGAGGGAGTTCA | 23072 |
rs186152976 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43164888 | CTGCAGGTCATCATA[A/C]CACAAGCTCATTCAT | 23072 |
rs186155201 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121481 | AGCAAATCATTTTCC[C/T]ATTTCTCCCAACATG | 23072 |
rs186157927 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126757 | ATTTTGGTAATTCTT[A/G]TAATATTTTAAGCTT | 23072 |
rs186186013 | snp | C/T | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358885 | GCTGGAGTGCAATGG[C/T]GTGATCTTGGCTCAC | 23072 |
rs186192388 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43317690 | TTTTCTTGTGTGATA[A/C]TTGTGATTAAGTGTT | 23072 |
rs186199221 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43454392 | TACTAATATTAGTTT[G/T]GGATCCATTAAAATT | 23072 |
rs186206213 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43494510 | ATAAAGTCAAGATTT[G/T]TTTTTTTTTTTGAGA | 23072 |
rs186210765 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43473963 | CAATAGGTGGAAACA[A/T]GATAAACTTAGATAC | 23072 |
rs186219551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43480566 | AAAAAATCAAAAATA[C/T]GGAGTAGGAAGGAAA | 23072 |
rs186221998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518273 | GCCAAGGCGGGTGGA[A/T]CACTTGAGGTCAGGA | 23072 |
rs186227545 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513294 | ACACTCTGGGACTCT[A/G]CTCTCCACGACGCGT | 23072 |
rs186233537 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43530614 | TTCTCTCCATACTAA[C/T]ATATGAATTCTAAAT | 23072 |
rs186239203 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159840 | GCCCACCACCACGCC[C/T]GGCTAATTTTTTGTA | 23072 |
rs186255499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123170 | ACCAGACGCTGGGCT[A/G]GGGGCCATTACCACG | 23072 |
rs186258952 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | HECW1 | GRCh38.p7 | 7:43375296 | TGTCTATTTAAAGGG[A/G]AAAAAAAAATAGTTC | 23072 |
rs186263725 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43419464 | GATTCCATCTCTTCA[C/T]TGTACTTTATAAGTT | 23072 |
rs186268377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43182846 | GTATTTGTGTCCTCT[C/T]CAATTTCTTTCATCA | 23072 |
rs186276435 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43411885 | TCTTCGGACTTAATT[G/T]CATTTATTACAATAA | 23072 |
rs186281507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43438454 | TGTACAGGTAGAAAC[C/T]AAAGTTTGTTTTACT | 23072 |
rs186282903 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43399105 | ATGACTCCTAAATCA[A/T]AATTTATAATCTTTT | 23072 |
rs186285252 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43449744 | CTCTGGCCCTTAAAG[C/G/T]CTTTTGCAAGAAAAC | 23072 |
rs186310768 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43512958 | GCTGACCTTCTTCTG[A/C]GTCCCATCCTCTTAC | 23072 |
rs186327143 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308118 | ATATAATATAACATA[A/T]AATATATTTATATAT | 23072 |
rs186334988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43283377 | GAATCCAGCTGTCTT[C/T]TGTTAAACCAGCTCT | 23072 |
rs186337799 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43338937 | ACCTATAGTTTTGAA[G/T]AGTAATTTCACAATA | 23072 |
rs186345476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43367688 | TTAGAATGACCTTTT[C/T]AAGGGGTTATTTTAC | 23072 |
rs186356924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43408758 | CCTGAGCTTGAAGCT[A/G]TAACCTCCAAACCAT | 23072 |
rs186364190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43327251 | TTCTGTTAGGAAAAA[G/T]TATGACTCCATATAC | 23072 |
rs186364613 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43349804 | GAGTTATCCATTCTG[C/T]GGTTCTGTATCTTTT | 23072 |
rs186369336 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43437832 | CAGAAGCATCTTGTC[A/G]CTGCCCCTCATTTAC | 23072 |
rs186372169 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43473444 | GTGAGAAAATGATAG[G/T]ATAAAAAGGACTAGT | 23072 |
rs186381145 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43230131 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 23072 |
rs186385322 | snp | A/G | 0.0610267 | 0.163674 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247856 | GGAAGAAGGAAGGAA[A/G]GAAAGAAAGAAGAAA | 23072 |
rs186388266 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43196645 | GCACACTTCTGACCT[G/T]AGCGGGAGATGGGCC | 23072 |
rs186392064 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43176482 | TTGGGAAGCCCAAAG[C/T]TGAGGGGCTTCATCT | 23072 |
rs186396440 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43265819 | AACTACAAATTTGAA[G/T]GTTCCCAAAACTCCC | 23072 |
rs186401189 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43469425 | AAATTTAGGTTTGGA[A/T]TGTGGAACTGAATTC | 23072 |
rs186408058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43451031 | GTCTTTCCCGACTCC[A/G]TGCCTTACAGTGTTA | 23072 |
rs186410981 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43489915 | AGACTTTGTAGCACT[G/T]GTCCTCATCACCTTC | 23072 |
rs186414212 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518043 | CTACTTTGAAAATAC[A/G]TGAAAAAAAGGAATG | 23072 |
rs186416991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43537737 | CTTAGAGTCATCCCG[C/T]CTGTGGTTATGTAAA | 23072 |
rs186423078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43560151 | TTTTCACCCCACTTC[A/G]CCTGTTTAGCCATAG | 23072 |
rs186427388 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140849 | GCTTTCTGGCTTCCC[A/G]GTGGCCACCACCTCA | 23072 |
rs186427813 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510234 | TCCATTCTGATGGTA[A/G]AGAGTGCTATGACCT | 23072 |
rs186453837 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43333379 | CACAGGATTTCAATC[G/T]CTTCCTCACAGGTAA | 23072 |
rs186490173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43192799 | CTTACTGTCACAGGG[C/T]GAACCCCAAAATTGG | 23072 |
rs186495771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43262518 | CCAGTCTTCATGATT[A/T]TAAAACTATGTTCTT | 23072 |
rs186500052 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43224716 | GCTACTCAGTAAGCT[C/G]AAGTGAGAGGATCAC | 23072 |
rs186507946 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163677 | AGTTGCCCCAGGTTC[A/G]ATCAACTAAGCTCCC | 23072 |
rs186526777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135739 | TTGAATTTTCACTCT[A/G]AAGCAGACTTTGTTT | 23072 |
rs186543779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43526069 | CAATATTATACTGAT[A/T]TAGTATTTTATTTGG | 23072 |
rs186554175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43390362 | TGGGCAACATAGTGA[A/G]ACCCCGTTCCTACAA | 23072 |
rs186555160 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43175616 | ACCACAAATAACTGT[C/G]AAAAATGCAACCAAT | 23072 |
rs186566197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189368 | TAGCTCTCAGGCGAT[A/T]GGGACATTGCTGGTC | 23072 |
rs186570730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43202748 | AGCCATCATATCCCC[C/T]GTGACCTGCATGTAT | 23072 |
rs186576822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43323756 | GGCTTGACCGTGCGC[A/G]GTGACTCATGCCTAT | 23072 |
rs186577042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43303616 | ATTTCTTTTTCAAAG[A/G]AAAGAAGCCCACACA | 23072 |
rs186584342 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122647 | GATCATGGTGTGACA[C/T]CCTTGAGAAAAATAG | 23072 |
rs186584555 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43279589 | CTTCATACCTTTGCA[C/G]AGGCTATGCGTCTGC | 23072 |
rs186588922 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43429081 | TACATACACAGAGAC[C/T]TTGCTTCCCATTCTA | 23072 |
rs186593594 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159043 | TGCTGGAGCTGCTGG[C/T]CTAGGGACCACAGCC | 23072 |
rs186594719 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43454167 | TTGTCTGCGAAGGAC[A/C]CCTTTCTTTACTGTA | 23072 |
rs186607863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43493470 | AATAGCTTCCATTAA[A/C]AAATTATTTATGTAC | 23072 |
rs186609689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43448090 | CAGTGAGCTGAGATC[A/G]TGCCATTGCACTCCC | 23072 |
rs186613447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43344408 | GTTCTCATTCCCTTG[C/T]CTTCCATTGTTTCTG | 23072 |
rs186616623 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43225584 | ATTAAACCAGAAAAC[C/T]CGAGATGCCTATATT | 23072 |
rs186616665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43187870 | CACTAAAAAGTGATA[C/T]ACTACAGCACAAGTC | 23072 |
rs186619835 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43201537 | AAGAAAAACAGTAAC[A/G]GAACAGCCAGTGTTC | 23072 |
rs186623052 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43243567 | CTCTTTCCCCACAAA[C/G]ACCCACACCAGATCC | 23072 |
rs186623837 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43486755 | GTGGCACATCACTGT[A/G]TGAACAATATGTAAT | 23072 |
rs186627818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43217261 | TGCATAGGCACTTTA[C/T]GCTTGAGTTCTGACC | 23072 |
rs186631072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43504534 | GTTTCTACCCTCTGG[A/C]AGAGCTTCACCCCTA | 23072 |
rs186633878 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43263570 | TTCACCATATTGGCC[A/G]GGCTGGTCTTGAACT | 23072 |
rs186636636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156779 | GTGGAATAAGTGGAA[A/G]TGATGTGTGTTACCT | 23072 |
rs186641136 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138282 | TTTCAACTTACATTT[C/T]CTCGGCTTATGTAGT | 23072 |
rs186642178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43173601 | CAACCTAGATCCCTC[C/T]CATGCGCAGTTCACA | 23072 |
rs186643615 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43488980 | TGGCTCAGCTTTACC[C/T]GTGAGTGGGTGACCT | 23072 |
rs186649557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43354956 | AGGAACTCCAGTTCA[C/T]CAGGCAGCAGACTTC | 23072 |
rs186653013 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43382618 | ATGTCTCTTTTAAAG[A/G]AATTTACTGACCCTA | 23072 |
rs186653858 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372208 | TTTAATTAATAGTTA[G/T]AAAAATTATTTCCAG | 23072 |
rs186658278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43391336 | GAAAACTCTCTTCCT[C/T]CCCAGTTCATCTGTA | 23072 |
rs186661655 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43313485 | TGGGATTACAGGCAT[C/G]TGCCACCACGCCTGG | 23072 |
rs186664662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242619 | TGAGTGCTCTGACCT[A/G]TCACAGAAATTGGAG | 23072 |
rs186667925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43349286 | TCATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 23072 |
rs186683303 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43430030 | TCAAACTTAACACAA[A/C]CCAAATCAAATTAAC | 23072 |
rs186683429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43409312 | TTTCTTCAGTCCTGC[C/T]TGTGTTCATCAATTA | 23072 |
rs186700263 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43239413 | CACAGGCTTTCCCTT[C/T]CTTCATGTACCGGGT | 23072 |
rs186701336 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43278480 | CCACCCATGCGGCCC[A/G]TTCTCATCACAGACC | 23072 |
rs186704163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43205859 | GGGCTGTTGGATGAT[C/T]TGTGGTCCACAGTGC | 23072 |
rs186707522 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43265296 | ACCTCAGCATGAAAG[C/T]TACACCTACTCTGCT | 23072 |
rs186726435 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43180757 | GAAGTACAATGTGAT[A/G]TCTCAGTACATGTGC | 23072 |
rs186740534 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307909 | ATACACATATATATA[G/T]ATATATATACACACA | 23072 |
rs186780346 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43549471 | CTCATTTGTCTTGCA[A/G]CATTGAGCATTGCAG | 23072 |
rs186784413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118796 | ATTGTCCTTGGTGTC[C/T]CCTCTACATGACCGG | 23072 |
rs186803530 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43275703 | TAGTCTGTTCTTATG[C/T]GCACGCACACACACA | 23072 |
rs186827661 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43340278 | CAGGCTAGAGTACAG[C/T]AGAGCAGTCTCAGCT | 23072 |
rs186827947 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43221940 | TGAGATGCAGATCCT[A/C]GTTACTCAAAATGTA | 23072 |
rs186832319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43544842 | AGCAATAAACAGGGT[A/G]CACTAACAACAATAA | 23072 |
rs186837044 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115610 | AAAAATGGGTGAAGC[A/T]ATGATTGGTCTAAAT | 23072 |
rs186837527 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43240109 | GCACTTTGGGAGGCC[A/G]AGGCGGGAGAATCAC | 23072 |
rs186840021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510584 | TAGCTTAAATGCTCA[C/T]TTATACGCACATATA | 23072 |
rs186840337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43460564 | TGCGTGTGTGCGTGT[A/G]TGTGTGTGTGTCCAT | 23072 |
rs186844480 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43432515 | TGTCCATCAGGCTGA[A/G]CCTTTGGGAAGCCTT | 23072 |
rs186848933 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43490797 | GAGTCTTGCTGTGTC[A/G]CCCAGGCTGGAGTGC | 23072 |
rs186849541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43259919 | AATAACAGCTGAAAT[A/G]TATGGGATACAATGA | 23072 |
rs186849695 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43468752 | GTCTCGAATTCCTGG[G/T]TGTTTACTTCTTGAG | 23072 |
rs186854783 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43528209 | AAACAAAATATTTCA[A/G]CTCTCCCAGTAAAGA | 23072 |
rs186860598 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509728 | CTCCAGAAAGCTGCT[A/G]GGACACCTGGGATGC | 23072 |
rs186861122 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43483852 | CCACGCCCAGCCACA[A/T]ACTTATATTTTTAAA | 23072 |
rs186868809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43203891 | GTATTTAATAGCTGA[C/T]AATTCTTGCTATTAT | 23072 |
rs186870954 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43367155 | ACTTGCCTCATTTCC[A/G]GTTCTGATTTTGGAA | 23072 |
rs186871142 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43550192 | ACTCAGGAGGCTGAG[G/T]CAGGAGGGTCATTTG | 23072 |
rs186911399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43403475 | TCTCTGGTGATCAAC[A/C]TTTGATCCCCCTGGT | 23072 |
rs186914495 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426648 | AATGATTTGGGTAGC[C/T]GTCCCTTTTTAAAAA | 23072 |
rs186919668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43504352 | TCCAATGTGCTTGAT[C/T]CACTACCCTTCCTAC | 23072 |
rs186927986 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43446074 | AACTAGCCCATGTAC[A/C/G]TACATATAGATATGT | 23072 |
rs186943608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43326702 | ATGAACATATTGGTG[A/T]CTTGGTGACAATTGA | 23072 |
rs186946234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389302 | CAGACTGCTGGAGCC[A/G]TCCCCAGACTTACAA | 23072 |
rs186949341 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363673 | ACACACAATCCCACA[A/G]GACTGTATTTTCACG | 23072 |
rs186958554 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43258404 | ACCCATTAAAAAGTA[A/G]TGGAGCTAGCATTCA | 23072 |
rs186958863 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43220148 | TTTTCTAATTTACTA[C/G]AATAACTTTCAGAAC | 23072 |
rs186964590 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43282536 | ATAAGAAGAGAGACC[G/T]AACATATGATTAAGT | 23072 |
rs186969264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439692 | TGCCCTCCCATGCTG[A/G]GTTCTCTCCTAAGTC | 23072 |
rs187002598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133235 | ATGATATACTTACAT[A/G]TGAAATATATACACA | 23072 |
rs187003252 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43323503 | CGGTGGAAGCATCAC[C/G]TGTACCGTGGAAGTT | 23072 |
rs187020318 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522767 | TGGCCAAACCCTGAA[C/T]TCAGCCCACAAGAAT | 23072 |
rs187025260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43364240 | ATTGTATGGTCTCAC[A/G]ATGCATCAATTCTTT | 23072 |
rs187025868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43278923 | TGTAGTCTCCTCCCC[A/G]TTAGGATTCAAGCTC | 23072 |
rs187032011 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43346101 | GCTGTACTAGTTTAC[A/G]TTCCCACCAGCAGTG | 23072 |
rs187034112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213971 | ATTAAACATTTCATC[A/C]GGATTTTGGAATTTA | 23072 |
rs187035003 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43324511 | AGAGATTGGCTCTAC[A/G]AAACGTTCTCATATG | 23072 |
rs187038510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43169605 | TGCTAGTACTTTGCT[C/T]TTGCCTAAAATGACC | 23072 |
rs187039244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43400696 | GCTTGCAAAAATAGA[A/G]ACTTAGAAAGTCAAG | 23072 |
rs187044084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420360 | TAAAATCCACAGCAA[A/G]CACTATACTTACTGG | 23072 |
rs187047318 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43380572 | TGCTCTTGTTACCTA[C/G]GCTAAGGTGCAATGG | 23072 |
rs187055255 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134254 | CAAAAAGTAGCCGGG[A/C/T]GTGGTGGTGCATGCC | 23072 |
rs187062835 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116773 | AAAACAGTATGAAAT[G/T]CTCTGTGGGGTTTTC | 23072 |
rs187070354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43185283 | GTGTCTCCTCCATCT[A/G]GCTGTTCACCTGTAT | 23072 |
rs187071179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148666 | AATCAAATAAGAAAA[G/T]AAGAGTGCATTGGGA | 23072 |
rs187073423 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43504937 | GAACTCTGGCCACCC[A/T]ATCCAGCGGGCAGTT | 23072 |
rs187087846 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523599 | AGCAGAGATCTCGCC[A/G]TTGCACTCCAGCCTG | 23072 |
rs187089739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43547366 | ATCCTGGCCAACATA[A/G]TGAAACCCCATCTCT | 23072 |
rs187120849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43554484 | AAATCAGATCAAAAG[C/T]AGCGGTTCCGTTCCT | 23072 |
rs187121597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153851 | ATTGAGATAATATTT[A/G]CTATTTTATTAGAAC | 23072 |
rs187131665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43379715 | CAGTTCCTCCAAATA[A/G]ATAATTCACTCCCTC | 23072 |
rs187132538 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118977 | GGTTGTCCCACTGGC[C/G]TTCTTCACTCCCTCC | 23072 |
rs187147596 | snp | A/G | 0.00835779 | 0.0641761 | intron-variant | HECW1 | GRCh38.p7 | 7:43343716 | ATTGTGAATAGTGCC[A/G]CAATAAAAATACGTG | 23072 |
rs187170960 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43488070 | ATCCCAGCACTTTGG[A/G]AGACCGAGGCAGGCA | 23072 |
rs187175317 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43465737 | GTGAAGGAAATAAGA[A/G]AAAAATAGCCAGGCA | 23072 |
rs187181932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43550148 | AAAAAATTAACCAGG[C/T]GGAGTGGGGCTTGTC | 23072 |
rs187187504 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43230417 | ATAAATAAAAACAAC[C/T]AGTGTCATGGAATAC | 23072 |
rs187196977 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43262953 | ATGAACAGTCACATC[A/T]CATGTCTGTTGAAAA | 23072 |
rs187198830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43404018 | ATTCTAGAACTCTAT[A/G]TGCTCTTATGGACAT | 23072 |
rs187208242 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43435782 | TGTTAGTGCAGCATG[A/C]CCTAGCTCATCCTGA | 23072 |
rs187211701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43443063 | AATTGTACAATGAAT[G/T]TTTATAATATCACAG | 23072 |
rs187212731 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481879 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCGTG | 23072 |
rs187216255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43480227 | ATTCCCACTCTATTC[A/G]CGCTCTACAATGTGC | 23072 |
rs187220369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43500003 | TGCCCAATGTGGCAT[A/C]ATAAATTTTCCATCA | 23072 |
rs187220471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518945 | ATAGCCTTTCAGGGG[A/G]GAATGCAATCCACAA | 23072 |
rs187230164 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43539841 | CTATTGGAGTAGAAG[A/G]TAACTGTTTTTATAC | 23072 |
rs187241787 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562085 | AAGCTGTGCATGAAG[A/G]ACTGCCTTCTTCTAA | 23072 |
rs187242330 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43233116 | TAGCTGGTTGTTACT[A/G]TCTCCCAGAACCTCT | 23072 |
rs187245636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253980 | CTGAGGAAACAGGCT[G/T]AGAGAAGTGAGGGGC | 23072 |
rs187247766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43361121 | ATATGGAGATATACT[A/G]ATAGATTGATTATGA | 23072 |
rs187260184 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43340700 | TAAAGCTACAGTGTC[A/G]TCTGTTGGTGGGAGT | 23072 |
rs187263912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43199144 | CTGAGAGCTCCCGCT[C/T]AGGGAACAGCCTCTG | 23072 |
rs187264596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43321772 | GTATATTTTGCTTTC[A/G]TTTTCATTCACTCTT | 23072 |
rs187265660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43200113 | TTCTCCTCTATTTTT[A/T]AAAAGTACTAGAAAC | 23072 |
rs187272098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43338007 | GAGTTGCCATGTCCT[A/G]TGTGCCAGAGAGCTA | 23072 |
rs187272217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43417073 | TTTATTTTTTGAGGC[C/G]GAGTTTCACTCTGGT | 23072 |
rs187274441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136248 | TTTTAATGCTTAGTT[G/T]GCACTTATCTATTGA | 23072 |
rs187276860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43459663 | CTACCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 23072 |
rs187279254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214797 | CCCCCAGAGAGGGGC[C/G]AGCTCACAGCCCACA | 23072 |
rs187280752 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377453 | AATTAATCTCAGGTT[C/G]TAGTAGAGCATTAGA | 23072 |
rs187283736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43395865 | TCCAATCACAACCTA[C/T]ACAGCATCAAGAATA | 23072 |
rs187284442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43234725 | TACTTATTTATTGTG[G/T]TTTTGGTTGCTCTCT | 23072 |
rs187284925 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43170792 | GTGGCCCAGCTGACC[A/G]TGCAAAGGTGGGGAT | 23072 |
rs187285315 | snp | A/G | 0.000582185 | 0.0170515 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444522 | GCAAAAGGACATCCA[A/G]CCTGCCCCCAGTGCA | 23072 |
rs187292203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130459 | TGTCACTATCTCAGG[C/G]ACCCATGTGGACAGT | 23072 |
rs187302694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43187388 | CAAAGAATCTGTGGA[C/T]GTATTTTGAACCACC | 23072 |
rs187305842 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43166476 | GAAGCAGCACCCAGG[A/C]CAGCTGCAGGGTGGA | 23072 |
rs187311201 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146167 | TGTCCTAATTTCCTT[G/T]TCCACTTAATTTTCT | 23072 |
rs187313093 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300272 | CCAGTCCTCCTATCA[C/T]AGCCTGCTGCTGAGA | 23072 |
rs187321344 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114269 | GATTTAGGAGGGCAG[A/T]TGCCCTACCCGAAAA | 23072 |
rs187347468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43498034 | GATATATGTAGGAGA[C/G]ACAGCTGGCATTCTT | 23072 |
rs187351804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43219328 | AAATGTTTCTGGAGC[C/T]GCTTCAAAAACGAAA | 23072 |
rs187353109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295799 | GTAAGGGAGCTTTTT[C/T]ATTGTAAGCCCATTT | 23072 |
rs187359086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43197203 | AAGAAAATTAGGAAA[A/G]ATGAGGAAAAAAAAA | 23072 |
rs187364498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257277 | CAGAATTGATCTGAT[A/G]TATTTGCTGCAGGAC | 23072 |
rs187378461 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43526738 | AGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 23072 |
rs187381207 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133807 | ATATATGTATATTTT[A/T]AATAATACAGTTTTC | 23072 |
rs187391858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43424710 | ATATCAATAGAGTTC[C/T]TGTGATATTGTAAAT | 23072 |
rs187408182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43383282 | GCATGATTTATGATC[C/T]TTTGGGTATATACCC | 23072 |
rs187411913 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141689 | TTTTAGTAGAGACAG[G/T]GTTTCTCCATGTTGG | 23072 |
rs187420430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43457571 | TGAAGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 23072 |
rs187421125 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124073 | AAGCTCTAAGATAGA[A/G]AACCTTCATTCTGTG | 23072 |
rs187426445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43496030 | GAGTGGAATGTATTT[C/G]CAAAAGGCAGTAGAC | 23072 |
rs187432186 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43476045 | TGTTCTAGAAGTACT[C/T]ACCAATATTACAAAA | 23072 |
rs187439943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514979 | CCCCATTCAAAGGCA[A/G]AGTCAGATATATAAT | 23072 |
rs187441548 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43533885 | CTGAGCTGTGATGCA[A/T]CAAAAGATGCAGAAG | 23072 |
rs187448516 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43267613 | AAGAAATTAATAAAC[C/T]ATAAACAAAATATAG | 23072 |
rs187452791 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43557532 | GGACTGTCACTGGAG[A/T]TGAGGTCAAGGAACT | 23072 |
rs187456488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43249511 | AGGGCCTGGACTGTC[C/T]TTTAAACATATTTTT | 23072 |
rs187456979 | snp | A/G/T | 0.00447939 | 0.0471367 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523213 | TTCTCCATGTTGGCC[A/G/T]GGGGGGGTCTCGAAC | 23072 |
rs187472641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43496220 | GAAACTAATAACCTA[C/T]TTTAAGGTTATGGAC | 23072 |
rs187473186 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43316905 | TTTCCCAGACTCCCA[C/T]GCAGCCATGTTCTGG | 23072 |
rs187482124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43440054 | GGGGGCCACTTCTGC[A/G]GTGCTGCCTCCTCCG | 23072 |
rs187487794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380130 | GTTATCAGGTTCACT[A/G]CAACTTTGACCTCCT | 23072 |
rs187488721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43211069 | GATAGATGATTGGCT[A/G]TTTCTTTACCTCCTA | 23072 |
rs187489129 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421742 | ACCACTGCACACTCA[C/G/T]CAGTGTGCAATGGTA | 23072 |
rs187490335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43455305 | ATACACTGTTAATTA[A/G]CAACTTATCAAAACG | 23072 |
rs187494502 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43231278 | GTCCCTCCCATCACA[A/G]CCCCTTGAATGTAAG | 23072 |
rs187497004 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43356379 | TATGCATATCTATGC[A/C]CCCAACACCAGAGCT | 23072 |
rs187509147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43184136 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC | 23072 |
rs187513496 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198331 | TCACTTACACACACA[C/T]CCTACATACACTCAT | 23072 |
rs187523471 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43272364 | AAGAGCTTCTGCATG[A/G]CAAAAGAAACTATCA | 23072 |
rs187541708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43236328 | CCATTCATGGGGGGG[A/G]AAAGCTCAAATGAAA | 23072 |
rs187543517 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315450 | TCTCCCCATATCTCC[C/T]GTCCCATTATTATTG | 23072 |
rs187582669 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43181251 | ATTCATGTCTTGATG[G/T]ATACTTAGGTTGTTT | 23072 |
rs187594515 | snp | A/G | 0.0020008 | 0.0315657 | intron-variant | HECW1 | GRCh38.p7 | 7:43206520 | ATGTGTTCTACTTCA[A/G]TTCTTTAGTGGTTAA | 23072 |
rs187597550 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145745 | GTGTTATCCAGAGGA[C/T]GGTTGTGAGAAACAG | 23072 |
rs187614136 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43183775 | ACTAATAAGACATAT[A/G]TTGGAACTTCACTTA | 23072 |
rs187615599 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43273627 | AACTCAAAAGAAAAT[A/G]TGGATAAATAAGTTA | 23072 |
rs187616000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43237856 | CCGCCCCCACTTGGA[G/T]CCTGCAAAAGCGCTG | 23072 |
rs187626106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145453 | GATATGTGCCACCAC[A/G]CCTGGCTAATTTTTG | 23072 |
rs187626848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43209882 | ATTGGCGTTCACCCC[A/G]AGGTCATCTGCCGTG | 23072 |
rs187631312 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43112958 | CGGGCGTAGCGCGGG[A/G]ACACTGTCTGCCGCC | 23072 |
rs187647148 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120740 | CCTCCGCCTCCCAGG[C/T]TCAAGTGATTTTTCT | 23072 |
rs187652926 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148189 | TAAAACAGGACAGAG[A/C]AGAAAGAAGGCCAGC | 23072 |
rs187653529 | snp | C/T | 1.65663e-05 | 0.002878 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43500735 | GACTGAGGGTAATCA[C/T]GGGCTTGAGAAGTTG | 23072 |
rs187656170 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43333453 | GGATTCCATTTGTAT[A/G]TGCATTTATAAAAGT | 23072 |
rs187656452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43314874 | CTGAGAAATGTAGAG[A/C]TGGTGATTTCATCTC | 23072 |
rs187659492 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43264595 | TCACGCCTGTAATCT[C/T]AGCACTTTGGGAGGC | 23072 |
rs187663250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43293300 | AGCAGACCCGAGCAG[C/T]GGTTCAAGGGCCCGA | 23072 |
rs187668761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116312 | CTTGCTCTGGCCTTA[A/G]AAGGAAACATGGCCC | 23072 |
rs187669850 | snp | C/T | 0.00375519 | 0.0431682 | intron-variant | HECW1 | GRCh38.p7 | 7:43541298 | CTTCCAACCCAGCCC[C/T]GTCTGCAGGGCAAGG | 23072 |
rs187671247 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43390843 | AAGCTGATTGAGCCA[G/T]TGCCCTTATACAATG | 23072 |
rs187673986 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43540843 | GTGGGCTTTTTATCT[A/C]AGATTTCTGAATTCC | 23072 |
rs187676157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43355617 | CACTAAAAATAAAAA[G/T]CAAAAAAACATACTA | 23072 |
rs187677838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43371271 | ATATACAACACTAAC[A/G]GTAACCACTGATGGG | 23072 |
rs187685077 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562436 | ATCTACTTTTCCCTG[G/T]GCATAATATCCATCC | 23072 |
rs187690108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43435045 | ATATAATTCATATTA[C/T]TGTGATCATGAATTG | 23072 |
rs187699006 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43394934 | GAGGGGGTGGAAGCT[A/G]GTGAGCCAGGAATGC | 23072 |
rs187713237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244256 | TACAGCTGAGAGCTC[C/T]GCTGTCTATGGGTAA | 23072 |
rs187719792 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43271469 | AAACCCTAAGGACTC[G/T]GTCAAAAGGCTATTA | 23072 |
rs187723954 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43470413 | GCCTTGGATTTCCAT[A/G]ACTGCAGCTTTTGCA | 23072 |
rs187726639 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43545395 | TAAAGTGTAGGAATT[C/T]GACAACTTAGAAAAA | 23072 |
rs187765885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43360680 | CTTGGATACAAAAAT[A/G]TTAAGGCCAGAACAA | 23072 |
rs187793836 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43364045 | GTGTCAACTTCTAGG[C/T]TGAGGATTGCTGCTG | 23072 |
rs187795915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43335343 | GCTTGACACATATGA[A/G]GTGGTTATGGTGACC | 23072 |
rs187804647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43255855 | GAGGGAGGAGGGAGG[A/T]CTTTATTTGGACTGA | 23072 |
rs187808159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210247 | TTGATGTGTCTGTTG[C/T]CACTGCCCAAAACGA | 23072 |
rs187813217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43293930 | GTAGGAGCATGAACC[C/T]TATTGTGAACTGCAC | 23072 |
rs187817965 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43191294 | CCCCAGACTAGAAGA[C/T]ACCTGAGGCCATTGA | 23072 |
rs187818329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43284362 | TTTTTTGTGGCGAGA[A/G]CACTTAAAATCTATT | 23072 |
rs187828922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248629 | AATTCTCTACACTTA[C/T]TGATTTGGAACCTCC | 23072 |
rs187843492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125260 | AACATGCGAATTTGA[G/T]GGGTGCAAACATTCA | 23072 |
rs187854850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43190576 | TCTCATAATGTATTC[A/G]GTTGTCCGGTGATGT | 23072 |
rs187856000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161189 | TGTCACTTTTTCAAG[A/G]GGCCTCCCTTTTGCA | 23072 |
rs187859010 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43194372 | AAAATCTGGGATGCT[C/T]GTTCATTCTCTGATC | 23072 |
rs187869343 | snp | A/C/G | | | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563059 | AGTTCCTTTGCATTC[A/C/G]ATTGTCCATCGGGAC | 23072 |
rs187872044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203516 | GAGGGCAGTGGCACA[A/G]TCTTGCTTATTGCAT | 23072 |
rs187877538 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129552 | TTTTGTTGAGATAGT[C/T]ACTTTATTGCAGTGG | 23072 |
rs187877971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43220686 | TCTAGGACACAGGAA[A/T]CCTAATCATTTTTGG | 23072 |
rs187881502 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166035 | AAAGATGAATTGGAC[A/G]TGGTTAAAAGTCTTC | 23072 |
rs187886218 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142338 | ATTCTTACTCGCACT[A/C]CAGTGTTCCCCTAGG | 23072 |
rs187889529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43556809 | TTGAATGTAATTTCC[A/G]TATTTGCTTTGGAAG | 23072 |
rs187894782 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43178137 | TCAGCCTCCAAAGTA[C/G]CTGGTACTACAGGTG | 23072 |
rs187900749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160792 | TTTCACAAAGGCCAA[G/T]AAAATTGTATCAAAT | 23072 |
rs187902337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351382 | AGAGAGTTTCGGCTG[C/T]AGTAGTATGCAGAGG | 23072 |
rs187906374 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43329044 | ACTGGGGAGACAAGC[A/G]TGTACTTCTTTTTGT | 23072 |
rs187910201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43309319 | AGGGTGGGGTGCAAG[G/T]GACGGCTTTGAGGCT | 23072 |
rs187911929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43534085 | AGACTTGGCATATTG[C/T]CTGGGTGCTGCACTG | 23072 |
rs187919540 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124827 | AATTTTATAATTTTA[A/T]GATTTTTTTTCTCAC | 23072 |
rs187921192 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43557887 | TTTTCTGCTCTATCC[C/T]ATTTCATTAAAATGA | 23072 |
rs187924487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43386042 | TGCCTGTTTCCTGTT[C/T]CCTTGCTGACTCAGC | 23072 |
rs187932558 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43410005 | GGAGGTGATCCAGGC[A/G]GTGCCGCTGCTGAGT | 23072 |
rs187934053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43394698 | TGAGGAAGGAATTCC[A/G]ATGAGACTGTAACTG | 23072 |
rs187936378 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43433523 | CATCCCAACATCTGC[A/G]CTTAAACAAAAGAAA | 23072 |
rs187939368 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43414846 | TTTGATCTGCTGCTG[G/T]ATTCGGTTTACCAGT | 23072 |
rs187943223 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43369426 | TCACGCCATTGCACT[C/T]CAGCCTGGGCTACAA | 23072 |
rs187946104 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43475315 | TGTAAGTAAATTTAA[A/G]CACAATTGTAAGAAC | 23072 |
rs187947665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43250648 | GGGTACAATCTAAAA[A/G]CCCATGCTGTCTCTC | 23072 |
rs187952875 | snp | A/G | 0 | 0 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520370 | GGACAGCCAAAGCAC[A/G]AGGACCACCTGCCTT | 23072 |
rs187955608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43392863 | AAGATCCCCTGCCAG[A/G]GTGAAAAGAGCTGAT | 23072 |
rs187963889 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43411382 | TTAAATTTATCAAGC[C/T]ATGTTTTACAGTCCA | 23072 |
rs187964738 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43448858 | GATCTCTTTCTGGGA[A/G]GTTCTGGCGGGTTTC | 23072 |
rs187968608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286465 | TTGTCCAGTTGACCA[C/T]TGCTCAGTTTTTACC | 23072 |
rs187969792 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43416685 | CAATCAGCGAGATTC[C/T]GTGGGCGTAGGACCC | 23072 |
rs187970863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514645 | TCATTTGCATATTGA[C/T]GAGGCACTCATATGC | 23072 |
rs187977325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268384 | AGATCTGCAGCCTAG[C/T]AGCCTTATTCCCTGT | 23072 |
rs187983532 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43432026 | TAGAGATGGGGGTTT[C/T]ACCATCTTGGCCAGG | 23072 |
rs187994397 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467636 | ACAGGCTGATTCAAC[C/T]GCTGAGTGAGAGATG | 23072 |
rs187995362 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43451893 | ACATTCTTTTGCCTG[G/T]GCTTACATGAAGCAG | 23072 |
rs188000736 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43449638 | TTGACCACCATTTTT[C/T]AGTCTCTCTCCTTTT | 23072 |
rs188016733 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43372534 | TCCCCACTGTTTTCC[A/T]TTTTTTAGACTTGTT | 23072 |
rs188046227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377016 | ATTCTTACTTCCCAA[A/G]GATCTCACAGAGCCA | 23072 |
rs188057770 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43304755 | CGCCTTGGCCTCCCA[A/G]AGTGTTGGGATTACA | 23072 |
rs188066653 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226212 | TTAGGTTCGGAACAT[C/T]GGGGTTAAAATGGAA | 23072 |
rs188075927 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43263747 | GGGAAGGAGACAAAA[C/G]GAAGGGAGGGAGGGA | 23072 |
rs188092598 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43194522 | ACCATAAGCCTGTGT[C/G]TGTGCTCCCTGGACC | 23072 |
rs188094197 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43308338 | GATATATTTATATAT[A/G]TTATATGATATATTT | 23072 |
rs188095987 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43178918 | GCAGCCTTTTCAGAA[C/T]ACTTCCTGAAAATAT | 23072 |
rs188098369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43230357 | CAAGATCGCACCACT[A/G]TACTCCAGCCTGGGT | 23072 |
rs188108717 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43266591 | CACCCGCCTCGGCCT[C/G]CCAAAGTGCTGGGAT | 23072 |
rs188119787 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142703 | TGGAATTTGACAACA[C/G]TTCCTGGAGGATCTA | 23072 |
rs188138149 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43197905 | ACAGGCCCCTGGAGC[C/T]GGCACTGGGCCCCTG | 23072 |
rs188144981 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137568 | TTTATTTATTTATTT[A/G]AGACAGGGTCTTGCT | 23072 |
rs188149909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43347520 | TGCCCTTTATTTCTT[G/T]CTCTTGTCTGATTGC | 23072 |
rs188161925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43307313 | TCCTATCAGTTCATA[C/T]TGTCTATCACCAAAG | 23072 |
rs188167296 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43529981 | TTGAGACAGAGTTTC[G/T]CTCTGTCACCCATGC | 23072 |
rs188169033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43553196 | CCTACCCACAAAACA[A/G]GTTCCTTATTACTTA | 23072 |
rs188175587 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121167 | CAGTTAAAGAGAGTG[G/T]CTAGCTTGAGCTTGT | 23072 |
rs188176546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43366004 | GCTACTTGGGAGGCT[A/G]AGGCACAAGAATCAC | 23072 |
rs188177543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43452402 | ATATAAGCCACTTTC[A/G]ATAATGAGAACAAAT | 23072 |
rs188191294 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43245726 | GACTGGGATCCCAGC[A/T]GATGCTGTCAAGGAC | 23072 |
rs188199618 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43219481 | TTCAGCTGGGAGCTT[C/T]GGCAAGACTCCTGTC | 23072 |
rs188205570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43237995 | TTGCATAATTCTGCC[C/G]CATCATATTGCTTTT | 23072 |
rs188214252 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43491230 | TAGAATCCTGGTTAT[C/G/T]CCCCTGTCTTACGGT | 23072 |
rs188219650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43281437 | TTTATCGTGGAAATA[A/C]AATTATTCCTCATTT | 23072 |
rs188221490 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43528877 | CAGCTAATTTGTAAA[A/C]TCATTTCCACATAAA | 23072 |
rs188225943 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43264714 | CCAGGTGTGGTGGCG[A/G]GCACCTGTAGTCTCA | 23072 |
rs188229257 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43430257 | GTAGCATCACCCTCA[C/T]ATCCATATCCTCATC | 23072 |
rs188239066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43455207 | CCTCTACAGTTTGTG[A/T]TGGTTATTTATCAAC | 23072 |
rs188239109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43495215 | GTTTGCTGCACCCAT[C/T]AACCCGTCATCTACA | 23072 |
rs188248351 | snp | C/T | | | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512449 | TATTCTCTAGTGAGG[C/T]ATTATCAGAAAATGC | 23072 |
rs188248939 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43385556 | CACCATGGCAGAGCC[A/G]TCCCTCAGAGAGCTG | 23072 |
rs188260008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43532745 | CATTCAGAAGGAATT[A/G]TTCTCCCCCATCATC | 23072 |
rs188268082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425576 | GCTATAATGGAATAC[A/G]ACAGACTGGGTAATT | 23072 |
rs188313727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43350805 | CCTTGCATTGGGCTT[C/T]GCCCTTCTGTGGTCC | 23072 |
rs188322536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43308810 | TACTTTTAGTAGAGA[C/T]GGGGCTTCGCCACGT | 23072 |
rs188351236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43279940 | TCCCTTCACTGGGGA[A/T]CTCTTCTGAGTTAGA | 23072 |
rs188355583 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43243786 | ATCTTGGCGGGGGTG[A/G/T]GGGAAACAATGTTGT | 23072 |
rs188356089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184747 | GACTGGGTAATTTAC[A/G]AAGAGAAGAGGTTTA | 23072 |
rs188360498 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198809 | GCACACACACATCCT[C/T]GCACACCCGCAGTCC | 23072 |
rs188364479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203286 | GATGTTCCCTAACTT[A/C]TTGAGATAGTCCTCT | 23072 |
rs188375425 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151776 | AGTGTATCCAACATA[C/T]GTTTATTCTCTTCAC | 23072 |
rs188383000 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43342941 | TGAGGCAGGAGAATG[A/G]CATGAACCTGGGAGG | 23072 |
rs188383836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117376 | CCACTCAACTTCCTA[C/T]AACATCCCCCACATA | 23072 |
rs188386837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369941 | AGCAAAATCAACTAA[C/T]TTACATCATTAAAGA | 23072 |
rs188389008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43388295 | CTTGGTTATTATGCA[A/G]TACAATAATGGCCAA | 23072 |
rs188393895 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149454 | AGACAAGGAAAGGCT[A/G]AGGAATTCTCATGGA | 23072 |
rs188396562 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155449 | TCCAAGATGAAAATA[A/G]GAAGAACAAGTAAAC | 23072 |
rs188397324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43322773 | GACATAATACTCGAA[C/T]GTGTGCACAAACCTA | 23072 |
rs188397505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43170301 | ACAATGTAATAATAG[C/T]AGAAATAAAGTGCAC | 23072 |
rs188399997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43177700 | GCACCTACTTCAACC[C/T]GTTTTGTGAAGGTTA | 23072 |
rs188401305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301477 | CCAAACTCTCCGAGG[C/T]TATGAGCACTGTTTA | 23072 |
rs188401871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43525648 | TAATCAAATTGAGAA[C/T]AGAACCAAGGTAGCT | 23072 |
rs188413335 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135637 | ATTATCCATCTACAC[C/T]TATCATCTTTTCATG | 23072 |
rs188415274 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43551594 | ATTTGAAAACTTCAA[A/T]GTGACTTAAGAAAGT | 23072 |
rs188416051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43549020 | CTCCCCACTGCTATC[A/G]CTAGGGTAGGCCCCC | 23072 |
rs188417462 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119867 | CCAGCACAGCCATCC[C/T]CGTCTAAGCGCTAGT | 23072 |
rs188419329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43362395 | CTCATAGCGGGAAGC[A/G]CAGTGGGAAGAGAGG | 23072 |
rs188420646 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118774 | TTTCCCCCTGCCTAC[C/T]CCCAGCATTGTCCTT | 23072 |
rs188423352 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43406792 | GCATGGTGATAGGCA[C/T]TTGTAATCCCAGCTA | 23072 |
rs188431225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242313 | GAGGGAGGTTTGGAC[C/T]ACGCTGGAGGAGGCA | 23072 |
rs188463397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43278100 | CCCCAAATGTATATG[C/T]CCATTTCAGACCCTG | 23072 |
rs188470231 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43261963 | CAGTGGTTTATGCCT[G/T]TAATCCCAGCTCTGT | 23072 |
rs188472142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43223930 | AATGCCACCTTCTCT[C/T]TCCTTTGATTGCCCC | 23072 |
rs188475499 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43470873 | AAGTAGCCTTAGACT[A/T]GCAATGTATTACCAC | 23072 |
rs188476903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43429380 | GGCTTACGTCTCAGC[A/T]GCATGGTCTCCGGCA | 23072 |
rs188481516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43401224 | TAAAAAGTACAATCA[C/T]AGAATTAAAAGCCTT | 23072 |
rs188486235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508403 | TCCTTTTTAGGTGGT[A/G]TACCCCTCTGAGTAT | 23072 |
rs188493984 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43365210 | TGATGCAGTCTGAAG[C/T]TGTTGGTGTGAGCCA | 23072 |
rs188505437 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511365 | CACTCTTTGGATGCT[G/T]CTGACTTGTGATGAA | 23072 |
rs188508182 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43464111 | GTGCTTGTGGAGCAA[C/G]GCAACTTTGTCAGTG | 23072 |
rs188519685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405121 | TAATCTCTACCTTGC[A/G]GAGTTTGTGTTCAGG | 23072 |
rs188522553 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43201430 | ACACAAAAAGGAGGA[A/G]GGATGCCCAGAAGTC | 23072 |
rs188526000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43368962 | ATCCTAATGGAAAGT[A/G]GAAATCCTTTCTATG | 23072 |
rs188547646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43315598 | TCCCAGGTTCAAGCG[A/G]TTCTCCTGATTCAGC | 23072 |
rs188559156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43294284 | GGCTTTAAGAGCAAC[A/G]TGTACATCCACACAG | 23072 |
rs188565938 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43325451 | GAACACTGAGATGAG[G/T]TGATCCTGAAAAGAA | 23072 |
rs188569627 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43272821 | ATCCCATTACTCTGT[A/G]TATTTCCAAAAGAAA | 23072 |
rs188570876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43285873 | TAGATAGCAAGCTAA[A/C]TCTTTTTAATCCCAG | 23072 |
rs188585264 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43254729 | TGCACCTCAGTTTAA[C/T]TACCATCTCTCTTCG | 23072 |
rs188586101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43456778 | GTGTTCCTTGAACTT[C/T]CCAGGCACTGTACCC | 23072 |
rs188597520 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43217828 | AGGAAAGGAACTATT[C/T]TTGGTCACTGAGCAT | 23072 |
rs188601292 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43328818 | AAGAAAACACTCAAT[C/T]GACATAAATAAAGGG | 23072 |
rs188601811 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237037 | TTCAGAAAGAAGAGA[A/C]TATAAAGGTAAAGTG | 23072 |
rs188605742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43196661 | AGCGGGAGATGGGCC[A/G]GGCTCCAGAGAGAGG | 23072 |
rs188620541 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43215596 | AATATCTATCCTAGT[G/T]GCTTTGCAGTCAGAA | 23072 |
rs188626141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256270 | AGATCTCATGGAGCA[C/G]TGTGAAAAGGGAGCA | 23072 |
rs188629933 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147642 | TTAAAATCAGGTCAT[A/G]TACCCTTTTTTTAAT | 23072 |
rs188632102 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43201701 | TAGACTCTAGACTAG[A/G]GAATCTTGGTCAGAG | 23072 |
rs188635699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43182993 | GATAGTTCACTATTA[C/G]CACATAGAAGTACTA | 23072 |
rs188637039 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156262 | TTCGTCAGCTTCATA[C/T]TCGCAGAGTCTCTGA | 23072 |
rs188638445 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43382352 | GTGTCTGAGGATGCG[A/G]TGAAGCAATGCCTGT | 23072 |
rs188639524 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43189975 | TAACATTCAATATTT[C/T]AGGAGCCAATATTGG | 23072 |
rs188639828 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43168297 | GACAAGGAAACATAC[A/G]GCTATTATACAGTAT | 23072 |
rs188644722 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43349226 | TTTAGTAGAGACGGG[G/T]TTTCTCCATGTTGAT | 23072 |
rs188646756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43366541 | CAAAAGGAATCCACA[A/G]GTTGCCGACTGATGG | 23072 |
rs188647282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43187600 | ATGTTGTTTGTGTGA[A/T]ATTTTGATTTTATGT | 23072 |
rs188656803 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132264 | TTGATGCAGTTTAAG[A/T]TGTGTCTTTTAATTT | 23072 |
rs188660446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160331 | TTTTTTTCATTCTTT[C/G]GTCAGAGCTCTCAAT | 23072 |
rs188667624 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43442159 | TTACATGAGATATCC[A/C]ATACTTTATTATAAA | 23072 |
rs188676760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424026 | TCAGGAATGATGGAG[C/G]AGGCAGGTGGGAGAG | 23072 |
rs188679382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519672 | AGGGGAATGGTTAAA[C/T]GTATTACAGCAGATC | 23072 |
rs188708067 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43551869 | AGGGGCCACCTTCTG[G/T]TTCATAGATGGTACC | 23072 |
rs188744720 | snp | G/T | 5.13967e-05 | 0.00506909 | intron-variant | HECW1 | GRCh38.p7 | 7:43445586 | GTTAGACCTCAAACC[G/T]GATCAGAGTGAGAAT | 23072 |
rs188755042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43483053 | AGAAAGGCTCACAGA[C/G]AGACAGTGACTAGTT | 23072 |
rs188773895 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43409193 | AGCTTTGAAGTGGAC[A/G]TGAGGGAAATAGACT | 23072 |
rs188776604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376296 | AATAATCTCACCACC[C/T]AACGAGCCTCAGGAA | 23072 |
rs188777940 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43447843 | AGAAACTGCATTAGA[C/T]GGCTGGGTGTGTGGG | 23072 |
rs188778049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380962 | CACTTCCACCAGCAG[C/T]GTATGAGAGCTCCAG | 23072 |
rs188794153 | snp | C/G | 0.0711525 | 0.174681 | intron-variant | HECW1 | GRCh38.p7 | 7:43340221 | CTAATTCCCACCCCC[C/G]ACCCCTTTTTTTTTT | 23072 |
rs188803623 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43486234 | AGTATTCCATGGTGT[A/G]TATGTGCCACATTTT | 23072 |
rs188804529 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43311252 | AGAGTGAAAGATGTA[A/T]ATGGAGGAGTGACTG | 23072 |
rs188810415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43288905 | CAGCCTACCTCTCTT[A/G]CCTTATTCTTATATT | 23072 |
rs188811747 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43306003 | AACCTCAGATGATCC[G/T]CCCACCTCAGCCTCC | 23072 |
rs188833591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43346609 | ATGTTATCTTCTAGA[A/G]TTTTTATAGTTTCAG | 23072 |
rs188834313 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43259339 | TTGCAGTGAGCTGAG[A/T]TCGCAGTGCTGCGCT | 23072 |
rs188834609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43501442 | TTCCCAATTCCCTAA[C/T]TGAAAATGCACTCTA | 23072 |
rs188836396 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43454168 | TGTCTGCGAAGGACC[C/T]CTTTCTTTACTGTAG | 23072 |
rs188840894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520567 | TTCATTCATGATTTC[C/T]TCATGATTTCCTGCA | 23072 |
rs188848481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43232850 | TCTTTAGGATAGCCA[A/G]TAATCGTCCTTTAAC | 23072 |
rs188851499 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198547 | TCACACTCCACACTC[A/T]CACACACCCTTCACT | 23072 |
rs188856484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43252243 | TCTTTCAGTAGCTCA[C/T]CTCTGAGCATCCTTC | 23072 |
rs188866968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298529 | GCACTGACATGATGA[A/G]TTTATCTCTGATAAC | 23072 |
rs188867606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269604 | GCTGGAGGAAATAAA[C/T]GAATTGAAAGGCAAG | 23072 |
rs188867766 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43185154 | AAGGACAGGGATGGT[G/T]GGGGGGAAGGGGCTG | 23072 |
rs188873155 | snp | A/C/T | 0.0372196 | 0.131242 | intron-variant | HECW1 | GRCh38.p7 | 7:43231820 | AGGAGATTGAGACCA[A/C/T]CCTGGCTAACACAGT | 23072 |
rs188883337 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43199100 | CCCTCATTGCACACT[C/G]TCTCTCTCCACGGTT | 23072 |
rs188888740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213201 | GGGTAACAAATCTTG[C/T]CCCAAGTGAGGTGTT | 23072 |
rs188891666 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43200597 | AAGATAAATACACAG[A/G]TGAGACACAGAGCTT | 23072 |
rs188899672 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43461734 | CTCTCTGTAATTCCA[A/C]CACCACTCAGCTCAT | 23072 |
rs188904225 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43235927 | GGCACGGTGGTTCAC[A/G]CCAGTAATCCCAGCA | 23072 |
rs188913532 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43399068 | ATTTGGGGGTAGTCA[C/G]AATCTTGCAGCCTCC | 23072 |
rs188913757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43483970 | GGAAGGGGATGAGGC[C/T]GAGTTGAGGTGACAA | 23072 |
rs188917781 | snp | A/G | 0.00160518 | 0.0282845 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43438047 | CGTGCTGGAAATTGA[A/G]GTGAAGGACAAGTTT | 23072 |
rs188921725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43419258 | TTGCAGTGACTGTGG[C/T]GGCATTCAGGGCAAA | 23072 |
rs188927117 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43173250 | GAGGAAAATTAAAGG[A/G]CCACTTTGCATGGCT | 23072 |
rs188944004 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137749 | GAGATAGGGTTTCAC[A/C]ATGTTGCTCAGGCTG | 23072 |
rs188977622 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112122 | TGTGCAGTGTAATAG[A/G]AAACGCGGTTTGGGA | 23072 |
rs188989483 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43455759 | ACTTTGGAAGGCTGA[A/G]GTGGGAAGATCACCT | 23072 |
rs188993428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43423171 | AATCATTCTCTGAAA[C/T]GCAGAGCTGGTACTG | 23072 |
rs189026433 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43426166 | TTTCCTATGAGCACA[A/G]AAGTGCCAAATCTGA | 23072 |
rs189036151 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358543 | CATCCAGGCATCACC[C/G]AGGTAATGGAAAACC | 23072 |
rs189036309 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43273801 | TCATATTTACAACAA[C/T]GGTGGATAATTTCCC | 23072 |
rs189043375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43460096 | TCACTGTTTTTTGTC[A/T]CAAGGGCCTGCTAAA | 23072 |
rs189043621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43500297 | TAGAGACAAGGTTTC[A/G]CCATATTCCTCAGGC | 23072 |
rs189048208 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43337599 | TACAGGATGGTATGT[A/G]CATGTACTTCATTTC | 23072 |
rs189052831 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43381821 | GAGCCACCACACCTG[A/G]CTGATAATTTTTTAA | 23072 |
rs189055136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125584 | ATATGGTGAAACCTC[C/G]TCTGTACTAAAAATA | 23072 |
rs189058792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358751 | GAGTCACATTTCCTG[A/G]TAGAAGTGTAAAGTG | 23072 |
rs189064586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43410601 | GTCTGTGTATAATTA[C/T]TATTTCTTCCTTAAA | 23072 |
rs189065487 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162266 | TGTGGCTTAAAACAA[C/T]AGAAATGTATTCTCT | 23072 |
rs189069895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143360 | TTGATCACAGCTAAC[A/T]GCAGCCTCAACTTCC | 23072 |
rs189071313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43316941 | AATTCGATTCATTTA[G/T]CTGCACCTGTGCAAG | 23072 |
rs189074923 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43373807 | ATTCTCCCCATCCTC[A/G]GAGCCCTTGGCAGCC | 23072 |
rs189078300 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359794 | AAAAAATATCTCAAA[C/T]TGGAGATTTCTCATA | 23072 |
rs189078634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43392210 | TCTGCCTCATTGTCA[A/G]TTTAATTGTTCTATA | 23072 |
rs189079950 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517310 | GATCCCAAGGCCCTT[C/T]GCTAACTGCAAAATA | 23072 |
rs189095738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43536216 | CAGGTCTAAATGGGT[A/G]GAAACACATCTCTAA | 23072 |
rs189097690 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43559568 | ATATATTATTATCCC[A/C]ACTTTACAAGTGAGA | 23072 |
rs189105049 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43208503 | GGTAGTTTTCTATCA[C/G]TGAGAGTCCCCAGGG | 23072 |
rs189106566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43274932 | TTAAAAACTATACAA[C/T]TCAATGCTGTTGAAG | 23072 |
rs189111715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43316209 | CTGAGGAGCAGGTGG[C/T]AGGATTCTACACACC | 23072 |
rs189119814 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43295361 | GGAATAGAATAGGAG[A/G]CAGGTTGGCCCAAGA | 23072 |
rs189130901 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147000 | TTATGGCTGCTTTAT[A/G]TGGCAGTGTATTTGC | 23072 |
rs189138513 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43240024 | TGTACTTTGTTTCTA[C/T]AATTAGGAAAAAAAG | 23072 |
rs189142743 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319539 | ACCCGCCCCCCACCC[G/T]CCGGCCTCCTTCCTT | 23072 |
rs189146912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43211146 | TGAGCTAAGTTGCAA[A/G]CCCTGTGTTTAGAGG | 23072 |
rs189147127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43182405 | CCCCATTTACTGAAA[A/G]GATTGTCCTTTCCCC | 23072 |
rs189151363 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115171 | GGCAAATAATTATAA[C/T]GTGAACCATGCAAGC | 23072 |
rs189156603 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43442973 | TGAATGAATGAATGA[A/T]CGTGAAACATCTTTC | 23072 |
rs189167037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43479381 | ACAGGAGGTGGAGCT[C/T]AAGTGGTAATGCTCA | 23072 |
rs189199445 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43543725 | CAGCAGTTACAGTGA[A/G]CCGAGATCACGTCAT | 23072 |
rs189214000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515771 | ATTTCAACATTTTTA[A/G]TATTTACCAAAACTT | 23072 |
rs189232599 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43491589 | AATTTGATTAATATT[C/T]ATGACTTTGACATGA | 23072 |
rs189236595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43471485 | AAGTAGAAGGGATGG[A/G]CAGAGCTGTTTGGTG | 23072 |
rs189240704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512040 | TTAACTGCCCACAGC[A/G]TGGGCGTAGCTGCTG | 23072 |
rs189244122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43437265 | CACCCCTTTCTTTTT[A/G]ACGAAGGCAGAGTTC | 23072 |
rs189254334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529474 | TACAATTCTAAATCA[C/T]ACTCCCTGACCTCAG | 23072 |
rs189257032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43473265 | TTCACCAGACACCCA[A/G]TCTTCCAATCAGCAG | 23072 |
rs189272414 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43207757 | TCCTGGCTTATTGTA[C/T]TTTAAAAAACATGGA | 23072 |
rs189272907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43375088 | GTTAAGAACATTGTG[A/G]AATTTCCTAAAATTT | 23072 |
rs189279591 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43441628 | TAAATATTTTAGGCT[C/T]TGCAAGGCCCACAGT | 23072 |
rs189280945 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43353544 | AGAACTCAAATATGA[A/G]GGTAAGACAGCTCTC | 23072 |
rs189281241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43370607 | ATCTTGGATGCAAGA[C/T]GTCCTTTAGCAGGCA | 23072 |
rs189282680 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43227410 | AGTCATTTAAAAAGC[A/G]TCTGGGTTTCAATGA | 23072 |
rs189287210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43417525 | ATATTTTCACTGGAT[A/G]TAGAATTCTGGGTTA | 23072 |
rs189297422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139672 | AGTTTTCCCTTATTT[A/C]TTTTCATTCAAAAAT | 23072 |
rs189299072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332312 | TGGAACCTCAACCCG[A/G]GCTGCTGAGACCCTC | 23072 |
rs189301211 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43408316 | AGTCTATGTTGTCTA[C/T]AAAGGCCCTTCTCCA | 23072 |
rs189302762 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43397680 | AGTATCACAAAATAC[A/G]TTATTGCAAGGGTGG | 23072 |
rs189303295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43436417 | CTTTGTCTGAGCAAT[A/G]AAGCTTTTTAATCAC | 23072 |
rs189305514 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122414 | TCTAATTTTTAGGTC[A/C]TCTGAAAGAAGCAAG | 23072 |
rs189306599 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43166784 | GAAAGGGCCCATTTG[A/T]ATTATTGATCTTAAT | 23072 |
rs189308734 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158465 | ACTGTTAATACTTTG[A/G]CATATATCCTACAAG | 23072 |
rs189311678 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296086 | TGTGTTAAAATGTTA[C/T]GGTTATTGAAATAAT | 23072 |
rs189313035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43182074 | CAGGCGTGAGCCACC[A/G]CGCCAGGCCTCTCAT | 23072 |
rs189314808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43195701 | ATCATGAAAGTTGGG[A/G]GATTTATTTGCAAAA | 23072 |
rs189319743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43453370 | GAGAAAGATAGGTAT[C/G]AAAAATGACCTAAGA | 23072 |
rs189321336 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43389373 | ATCAAGCCCTGTAGG[C/T]GATTCTGATGCATGC | 23072 |
rs189330601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257535 | TCTGATGGAGGGGTA[A/G]CAGCAAACCTCCAGT | 23072 |
rs189331516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146525 | AACTGGTGAAAAGGG[A/G]AGAAAGGGAATGGAA | 23072 |
rs189344917 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43402251 | AGATGGCAGAGCTAA[A/C]GGAGCACTGTAACTC | 23072 |
rs189350131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43312180 | TAATTAAAATATACA[A/G]GCAACTGTGTTATAT | 23072 |
rs189350519 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43338331 | TACTTCATATTCTTC[A/T]CTCTTGCCTTCTATA | 23072 |
rs189351571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43330501 | GCTGTCAAGTTTTTG[A/G]TTTGATGATTATACA | 23072 |
rs189357448 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43290950 | CAGGATGAAGTTTCC[A/G]TCAAGAGAAGACTGC | 23072 |
rs189360238 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43251371 | CTGGAGTGCGATAGC[A/G]CGGCCTTGGCTCACT | 23072 |
rs189371730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43288154 | TTCTTTCTCTAGGGC[A/T]TTTTCAATTAAACAC | 23072 |
rs189385351 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43196586 | GAATCTCTTGCCTCA[C/T]TGATTTAATGCCCTC | 23072 |
rs189387783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43212250 | CTCTCTCAGATTAGG[C/G]TTGTGTTATTAATTA | 23072 |
rs189391946 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192612 | ATTAATAACTTACGC[A/G]TGCTTATTTTAAGAC | 23072 |
rs189404603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43228515 | AAGAACTATGGGAAC[A/G]CTCAATGTTGTTGAG | 23072 |
rs189410983 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43167493 | TCAACAACTCCAGAT[C/G]GAGGGAGGTTGGAAG | 23072 |
rs189449507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131364 | ACCTGAAGTGTTTCT[A/G]TGGCTTGACCAGCTC | 23072 |
rs189449676 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118436 | TAAGGGGGGAAAAGA[C/T]GGGGAGAATAAAATT | 23072 |
rs189473823 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488434 | AGAGAAAGAAAGAAA[A/G]AGAAAGAAAGAAAGA | 23072 |
rs189477012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521673 | CTGAAGTCAGGAGTT[C/T]AAGACCAGTCTGACA | 23072 |
rs189490385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43524945 | ATTTAAACTGAGGAG[G/T]TTTTCACGAGAATCA | 23072 |
rs189494057 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43507691 | ATATTTTCCCTTCTG[A/G]GTTTATTATTTTCAT | 23072 |
rs189495854 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516751 | ATCATTGCGTGAACA[C/T]CATAGAGTGGAATTA | 23072 |
rs189499899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43488846 | GGGACGCAGCAAGCC[A/G]TATCTCCCCCTGTGT | 23072 |
rs189516008 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43204863 | CCCCGCAAAGTTTGG[A/G]TCTTACCATCCCACA | 23072 |
rs189519001 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43558556 | TTGGTTGAGGGGAAG[A/G]GGTGCTACTGGTGTC | 23072 |
rs189522087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43418180 | GGACATCAGTCATAC[A/G]GGATTAGGGCCCACC | 23072 |
rs189524575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43223156 | ACATTCAGTTTAGCA[A/G]CAGATCCTTTGCTTT | 23072 |
rs189529241 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43368147 | ACAAATCCCCATGCT[C/T]ATCAAGCCACCTGCC | 23072 |
rs189534318 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43241838 | ATTTTTAAAACTGTC[A/C]AAAAATAATAACTAC | 23072 |
rs189539993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43349859 | ATTCAATGTAAGTAT[C/T]GAAATATGAGGTACC | 23072 |
rs189541830 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43327286 | CTGCAAGATAATAGG[C/T]GTATTTATATTATTG | 23072 |
rs189543877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43179719 | ACTGCAGCATAGAAT[A/G]TGACTGCCTTAATTT | 23072 |
rs189545907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162742 | CCTTTTAATACAGAG[A/G]TAGTGGTCCCTATAA | 23072 |
rs189553323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43492957 | AGCTTGCATTTTTTT[A/G]ATGAGTATGCTGCCT | 23072 |
rs189561411 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43383377 | TCTTCCACAATGGTT[A/G]AACTAATTTACACTC | 23072 |
rs189562460 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43192263 | CACGCCTGGCAAGAC[C/T]TAGTATTAATAGATC | 23072 |
rs189571013 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43352592 | GGTCTGCCATGAACC[A/G]TATGTGTGACCTTAT | 23072 |
rs189579813 | snp | A/C/G | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43264794 | GCTTGCAGTGAGCCG[A/C/G]GATCGCACCACTGCA | 23072 |
rs189584740 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144137 | TTGTTTTTGATGACC[G/T]TGACAGTTTTGAAGA | 23072 |
rs189595476 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308125 | ATAACATATAATATA[G/T]TTATATATAATATAT | 23072 |
rs189601935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43378835 | AACAAAAGAAGGAGG[C/T]AATGTCAGGCAAGGG | 23072 |
rs189604626 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43283819 | TGCTTTTTTAATGCA[A/G]CAATCTATTTCCTCC | 23072 |
rs189611166 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269033 | CAGTGCCACCCTCTA[C/G]CCACTCTCTCATGTC | 23072 |
rs189614374 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43307472 | GAAAGGAGGTCTCCT[A/G]TTGGGGAGATCTGCT | 23072 |
rs189615229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43266063 | TTTTTTATGGAGGCT[A/G]CATTATGTAGGCATG | 23072 |
rs189627386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43336516 | CCTCTCAGGACTCTG[G/T]GCAGACCATGACTTT | 23072 |
rs189632622 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43232409 | GAAATGGAGGCTGGC[G/T]GTGCAACTGCATTAG | 23072 |
rs189642394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43205505 | GAAATCACTTGTGCT[A/G]CAAGTCGTAGTTCTT | 23072 |
rs189648541 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43310726 | GTCTGCTCATCATAG[A/C]TGGTAAACAAAAAGT | 23072 |
rs189656559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43229156 | ATTAGATACGTTTCC[A/G]GTGTTGAGCTCTCTC | 23072 |
rs189675767 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43180256 | TGGCTCCTGGGACAA[A/G]CTGTGTAGGTAGAGT | 23072 |
rs189688060 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139077 | GCCATTTTAATTGGT[C/G]TTCTTTTTGTTTCCA | 23072 |
rs189710135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43174169 | GATAGGTGGAATTTC[A/G]GAGCATACTGGGAAG | 23072 |
rs189722547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43485467 | GGATACATTCTGAAA[A/G]TGTTGTTGTTAGGCA | 23072 |
rs189733732 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43503314 | AAAAGTAAGGGGTTT[G/T]GGGGGAAAAGTTTGG | 23072 |
rs189751771 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43202883 | CAGAAGCTCCCCAAC[A/G]GAGCACCTTGTGACC | 23072 |
rs189755463 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43493608 | TGTTCTAACTACTTA[A/C]ATCTTATGCTTCATT | 23072 |
rs189761150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43496868 | GGGCATGGAGGTGGT[C/T]CTTCAACTAGTGCTT | 23072 |
rs189763348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43364151 | GACAATACGCTAAAC[C/G]TACCATTCTTTGAAA | 23072 |
rs189767813 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43408615 | TTCTTGAGCCTGACA[C/G]GCAGAGGTTGTAGTG | 23072 |
rs189774538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43175809 | TGCAGCCTTCATGAC[A/G]GCTTTTGGTTGTTCT | 23072 |
rs189776731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43530275 | TGCTTTACTGTAATC[A/G]ACACTTTACTGCAGT | 23072 |
rs189781847 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43323789 | TCCCAGCACTTTGGG[A/G]GGCCTAGGTAGGGGG | 23072 |
rs189783524 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468491 | TCACAGATAGTCCAT[A/G]TGGGCCAAGGGGGCA | 23072 |
rs189783933 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43345540 | ACCCATCACCCATGT[A/G]TACACCACAACATAC | 23072 |
rs189784273 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43389936 | CCCACCTGGCCCCCT[A/C]ATTATTTTTAGTAAG | 23072 |
rs189786389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43189475 | GATTGTGTGCAGGTC[A/G]CTTTGCTAGTACTTT | 23072 |
rs189788085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43447195 | GTATTAAAAAGTGTA[A/C]TGACACTTTTCTTAG | 23072 |
rs189789737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43535684 | CTATTTGCATGTATC[A/G]AGGGTGTCCGTACTG | 23072 |
rs189794462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428765 | TAAAGTAGGCACAAG[A/G]AGGTCAGTTACATTG | 23072 |
rs189798368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427636 | ATTATCTCACAATTC[G/T]GTAGGTCAGAAGTCT | 23072 |
rs189799506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43556570 | GCATGCACCGGTAGT[A/C]CCAGCTATTTGGGAA | 23072 |
rs189803579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122844 | ATAAAACTACATACA[C/T]ATAACATATATAAAC | 23072 |
rs189804771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43380220 | ACCACACCTGGCTAA[C/T]ATTTTTAAAAATTTT | 23072 |
rs189806254 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43388632 | GCTGGATATTCTGGG[A/G/T]TTTTTTGTTTTGTTT | 23072 |
rs189811694 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116517 | ATGACCTACAGTTAG[A/C]CCAGAGACAACCATC | 23072 |
rs189813134 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43263623 | CTCAGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 23072 |
rs189816406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139978 | ATGAGAAAATGCATC[C/T]AAAGTTCTTAGCCCA | 23072 |
rs189848881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43304506 | TTTATTTATTTATTT[A/G]TCGATATGGAGTCTC | 23072 |
rs189855101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43279632 | CCCTCCTTGTCCCCA[C/T]TTCATTTGTTCTGAA | 23072 |
rs189878400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43246220 | AACAGGGAGAATCGC[C/T]TGAGCCCAGGAGTTC | 23072 |
rs189880679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43326501 | ATGTCCTCCACAAGG[C/T]GGCCCCATGAAGATG | 23072 |
rs189888200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43353373 | ATTAAAATACTCGTT[A/T]AAGAAAAAGGAAAAC | 23072 |
rs189888654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43356605 | CATTTTTTCTATCAA[C/T]ACATGGAACATTCTT | 23072 |
rs189892805 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281886 | AATTGGATTCTTATG[A/G]CATCCTGCATGTGCA | 23072 |
rs189895368 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43531347 | CCACTTGCTCTGTGG[G/T]GATGAGATACTGCAT | 23072 |
rs189907083 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43209275 | CCCCTGAAGACCCAT[C/G]CTCCCCTGTCCCCTG | 23072 |
rs189929776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43240533 | AGTATGGTCTGAAGG[A/G]TAACGTGCTTTCTAA | 23072 |
rs189930555 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43188075 | ACAGGAGTGGCTTAC[A/C]TTGTGAGGGATGTTC | 23072 |
rs189931511 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43275809 | TAGGTGGCTGTGGGT[A/T]TATTCAATCAAATGC | 23072 |
rs189937015 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179374 | AAGTGTGGTAAAAAT[G/T]GCAACCTTTGCTTGA | 23072 |
rs189957318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43204121 | GAACTCTTATACCTT[A/G]GCACCATAATAAATA | 23072 |
rs189959078 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152568 | ATAAGGGTACAATAT[G/T]GCTTTGTTGTTGTTG | 23072 |
rs189964619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43498460 | GGTCATTCATAAGGC[C/G]AAAATCATTAAATTA | 23072 |
rs189965178 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157042 | GACACATGTTCATTC[A/G]CAAACCTGGGCTTTG | 23072 |
rs189966550 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43480648 | GTGTGTACATATGTG[G/T]GTGTGTGTGTATATA | 23072 |
rs189978803 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118809 | TCCCCTCTACATGAC[C/T]GGGCATAGGACCTGC | 23072 |
rs189983901 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121379 | GAGTGGCCAAAGTAC[A/G]CACAATTCCCTAGGC | 23072 |
rs189988689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43548030 | GTACAGTATGTACTA[C/T]AGTTAATTTTATGCA | 23072 |
rs189999919 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43473457 | AGTATAAAAAGGACT[A/G]GTGGTGAGTATTTAA | 23072 |
rs190004712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214784 | GAAGGAGGAGGAACC[C/G]CCAGAGAGGGGCCAG | 23072 |
rs190013784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43404762 | AGGTAGATCACCCTA[C/T]GTCAAGAGTTTAAGA | 23072 |
rs190020834 | snp | A/G | | | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43512976 | CCCATCCTCTTACAC[A/G]TTTTCTGAGTTCCCT | 23072 |
rs190022969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43171943 | CAGATAAAAGATTTT[C/T]ACAGTTGCTCAGTGT | 23072 |
rs190026280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43368399 | TTAACCCAGAATATA[A/G]TGGCAGCTTATTCAT | 23072 |
rs190034902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43444087 | TCTGGCCAGTGAGAA[A/G]CCCTCATCAACCTAC | 23072 |
rs190037851 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43186272 | TTGTGCTTTATAAAT[C/T]ACCTAAAAGTTAGTA | 23072 |
rs190041764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43553982 | CAGTCAATGGCAAAT[C/T]GTTTAATTGATATAT | 23072 |
rs190042278 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43200031 | TTTTTATAAATCCTT[C/T]TAGGGCTCATGCCAA | 23072 |
rs190046480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425054 | GCACAAGTCCAGTGA[C/T]TGATAGAGTAATCAG | 23072 |
rs190048030 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43459081 | CCATGGCAGGAAAAT[G/T]CCTCCCACCTGCCTC | 23072 |
rs190049224 | snp | A/C/T | 0.00835923 | 0.0641982 | intron-variant | HECW1 | GRCh38.p7 | 7:43430908 | TGCCTCAGCCTCCCA[A/C/T]GTAGCTGGGATTACA | 23072 |
rs190052937 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119475 | TGACCTTTAAATGCG[C/G]GTACGGGGATTCCCC | 23072 |
rs190053467 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43466621 | GGCAAGACCCAAAAC[A/G]CAGCTTTGTAAAGTC | 23072 |
rs190057765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43403888 | CTATTTTTTCATTCT[A/G]TATTTTTAAGTATTA | 23072 |
rs190064598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154788 | TAGGTTCTAAGATGC[A/G]TTTTTGCAGAGTGAT | 23072 |
rs190065620 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43408003 | GCAGGACGGCCTTTC[C/T]CTCTGCCCTTCATGT | 23072 |
rs190068115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43506041 | AAATTAAAAGGTATA[A/T]ATAGTAAAGTATTTA | 23072 |
rs190068677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136682 | TTCATCTAAATTACC[C/T]TCTCAAACAGATCAC | 23072 |
rs190078011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43446432 | ATTGAAAAGTCACAT[A/T]ATAATATGAAATAAT | 23072 |
rs190116796 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43367328 | TAACCAGCACTAAAA[A/G]GAAACCTCATTAACA | 23072 |
rs190121253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43370201 | AAATGGGCAAAACAC[C/G]TGGATAGATATCTCA | 23072 |
rs190138167 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43332039 | ACGCAGGTGGCAGGT[A/G]CAAGATGGGAACAAA | 23072 |
rs190139691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256812 | ATCCCCCTTCTCTGC[A/T]TCTGGCTTCCCCTCC | 23072 |
rs190166746 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43219148 | TGTTCTACACATGTG[A/G]GGATATGTGGGAGTG | 23072 |
rs190175723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222415 | ATGTCCAGAAGGTAC[C/T]TTGTATAAGAGGGAT | 23072 |
rs190191576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43260462 | TTATAGGACACAATA[C/T]GGATTATTGTTTTCA | 23072 |
rs190197894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136106 | TCACCTTTGGACAGT[A/G]AAACAATCCAGGCTG | 23072 |
rs190205460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189060 | TCGCTTCCTTTCTCA[C/T]GGTTGAGTTGAATGC | 23072 |
rs190205890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43170659 | TCAAAGGTGCATGGT[A/G]TGTATTAACAGAAAG | 23072 |
rs190206620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522420 | ATTTGCTTCCCAAGA[C/T]AGTTGCCTCCTGGAC | 23072 |
rs190207221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43339079 | TCTTCCCCCATCTTA[G/T]GCTTCTAAGACTTTT | 23072 |
rs190209191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43318031 | CTGAGAACATAGACC[A/G]TGACTTGTTCACCAG | 23072 |
rs190212506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43544469 | AGAAAATTTACCAGT[A/G]TTTTGGGATGGTGTA | 23072 |
rs190227257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115579 | CTCAAAACTTGCTAG[C/T]GCTGTTGCTTGTCAC | 23072 |
rs190238422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131133 | TAGATGGGCGTGGTG[G/T]CACACGCGTGTAATC | 23072 |
rs190247348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210336 | ACTTGCAGAGTATGA[G/T]GCCCTGGGTGGCTCT | 23072 |
rs190272069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296686 | AATGAGGCCAAATGC[A/G]AACTAATGGAAAAAA | 23072 |
rs190276281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43274050 | GAGACGGGGTTTTGC[C/T]ATGTTGACCAGGCTG | 23072 |
rs190282453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43219901 | ACAAAAGGTTCTTTT[A/G]TGGGCAGGAAATGGA | 23072 |
rs190283949 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43485937 | ATTTGTATACATGTG[C/T]CATGTGGGTTTGCTG | 23072 |
rs190286456 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43258066 | CAGTAAAGGCCAGGC[A/G]TGGTGGCTCACGCCT | 23072 |
rs190289052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43449301 | GTCCACAATGAACTG[A/G]GTGCCGGCATGAGGG | 23072 |
rs190291644 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43446803 | AAAACAGACAGCATG[A/G]AAAGGTACCCACAAG | 23072 |
rs190293049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424357 | AGGTGCAGTGGCTCA[C/T]GCCTCTAATCCCAAC | 23072 |
rs190294354 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43238432 | GGGAGGAGGTGGCCA[C/T]ACCCACAGGTGGTCA | 23072 |
rs190302411 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43504120 | AAGGCCTGTGGCCCC[G/T]GCCTTGTAGTCTTCC | 23072 |
rs190319259 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488370 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 23072 |
rs190324473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521083 | CTATCTGAGTCTCAG[C/T]CTCCTAGTTCACCAA | 23072 |
rs190336774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524220 | TTAGCAGCGTCAAGA[A/G]TCTTTCAAAGAGTGT | 23072 |
rs190359311 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43378497 | AGACATCCCAAATAC[G/T]CATGGTTAAAACCCT | 23072 |
rs190370287 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43382669 | ATAGACAGTGGATCT[A/G]TCCCACCAGATGGAA | 23072 |
rs190387489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43349438 | TTAATGACCTGTCTA[A/G]TGCTGTCAGTGAAGT | 23072 |
rs190389232 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300595 | CCTGCTTCACTCTTC[A/G]TCATGGCTCTAAGTT | 23072 |
rs190404979 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43261490 | GCCCCAAGTGCAAGG[C/T]AGTTTAAACCCTTGG | 23072 |
rs190419607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43342658 | ATTGCTTTTCTTGGG[G/T]TTTGAGGATATAGTC | 23072 |
rs190423035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43237315 | ACTGGAGAAGACCTG[C/T]CTGGAGCCCTCCTCG | 23072 |
rs190427212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43273274 | AAACCTCAGAATCAC[A/G]CAATATACCCAAGCA | 23072 |
rs190428370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43163699 | TAAGCTCCCCCAAAT[A/G]GCTCTGCTTTAATTC | 23072 |
rs190430488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145110 | AAAATAAATTACTAA[C/T]TCTCTCAACAGAAAT | 23072 |
rs190439186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43180924 | TCACCCTACTGTGCA[A/G]TAGAATAGCTGAACT | 23072 |
rs190444639 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43379485 | GCATAGTCCACTGTC[C/T]TCTCCGCTCAATCAC | 23072 |
rs190445556 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43175385 | AAGTGACATTTTGTA[C/T]CCTTTGACCAACATC | 23072 |
rs190451418 | snp | A/C | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112029 | GTAACCAGCATTTCA[A/C]TTCTCTTTGCATCTC | 23072 |
rs190452716 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43333387 | TTCAATCGCTTCCTC[A/G]CAGGTAAATCCAGAA | 23072 |
rs190457907 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43202538 | GAGTGCAGTGGTGCA[A/G]TCTCGGCTCACTGAA | 23072 |
rs190461418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43540024 | TTTTGTTTGACTCTA[A/G]TCTCTTCAGAGTCAA | 23072 |
rs190464691 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43363037 | TTATTTAAATAAAGC[A/T]CCCTAGAGCATTTGT | 23072 |
rs190464812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43313519 | GTTTTGTATTTTTAG[C/T]ACAGACAGGGTTTCT | 23072 |
rs190465663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127939 | ACTGGCATGTAGTAG[C/T]ATGATCACAGCTCAC | 23072 |
rs190465842 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562086 | AGCTGTGCATGAAGA[A/T]CTGCCTTCTTCTAAG | 23072 |
rs190488881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43543186 | ATTTTCTAGACCTAA[A/T]GTCTGTGACATAAGG | 23072 |
rs190490462 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43170156 | ATTCTCATAGGAGCA[A/C]GAACCTTATTGTGGA | 23072 |
rs190494632 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | HECW1 | GRCh38.p7 | 7:43254205 | GGCTCCAATTTAGTC[G/T]TATCGTCAGGTCTTT | 23072 |
rs190495374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114663 | TATTTAATAATCCAC[A/G]TTCTGACTAATTCCA | 23072 |
rs190496508 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110967 | GTATAAAAAAAGCAA[C/T]TCCTCAGGGGAGGAT | 23072 |
rs190513947 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293242 | AAAAAAAAAAGAAAA[G/T]AAAAGAAAAAAAAGA | 23072 |
rs190515643 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43200228 | TGAATGGCATTAGTT[A/G]TACTTATTTTATTAG | 23072 |
rs190519901 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43343344 | TTACATAGGTGTACA[A/T]GTGCCATGATGGTTT | 23072 |
rs190523920 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215078 | GTTCTTTTTATCCTG[A/G]TTTTAAAAAATGTAA | 23072 |
rs190526017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43271185 | AACCAAGAAACTTTG[C/G]GGAAAGAAGTGTGGA | 23072 |
rs190527323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134786 | TTTGTGTTGTGACTT[C/T]TTCCCCAAGACTCTT | 23072 |
rs190528448 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43481964 | TGAGCGACACAGCGA[G/T]ACTCCATCTCAAAAA | 23072 |
rs190533391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43234952 | TCGCCTTTCATGACT[A/C]TCTGGGTCCCTGTGC | 23072 |
rs190543792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519304 | AGGCTGGAGTGCAAT[C/G]GCACGATCTTGGCTC | 23072 |
rs190545469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43500202 | GCCTCCCGGTTCAAG[C/G]GATTCTCCTACCTCA | 23072 |
rs190555706 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43462090 | TCTGCAGAAATCCTG[C/T]CATAGTGGAGCCTCA | 23072 |
rs190563464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43502679 | AAACAAACAAACGAA[A/T]AAAAAGATATTTTCT | 23072 |
rs190590512 | snp | C/T | 0.000116031 | 0.00761592 | intron-variant | HECW1 | GRCh38.p7 | 7:43396902 | CAGGTATGTTTTGCT[C/T]ACCTGAGACTTTGTG | 23072 |
rs190596046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43320243 | GGAGATTTTTTCTTT[A/G]TGTCTCGCCCTTAGG | 23072 |
rs190616152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283070 | TTGCAGTGAGCCGAG[A/T]TCATGTCACTTGTCA | 23072 |
rs190619324 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43424752 | GCAATTTTGTCACAA[C/T]GGAATTACTGTGGTT | 23072 |
rs190624866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428149 | CAGTGCCAACCCCAC[A/C]CCAGATGAAAAGTTT | 23072 |
rs190631012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359999 | CTGATGTTGTCATTT[A/C]GTCATCACATCATCA | 23072 |
rs190647084 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43277059 | GGGCTCTTTGGTCTC[A/C]TCCTTTCTCTAGTCC | 23072 |
rs190659384 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247394 | GGCTCATGCCTGTAA[G/T]CCAGCACTTTGGGAG | 23072 |
rs190661927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43210072 | TTTAAGTCAACAGCC[A/G]GGGACTGGCAGTTTC | 23072 |
rs190667212 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43361774 | TGGACAGAAACCAGT[A/G]GAGGACTTTGTCATG | 23072 |
rs190675657 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248037 | AAGCAAGCAAGAAGG[G/T]AGGGAGGGAGAGAGG | 23072 |
rs190676011 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43183605 | AATAAAATATAAAAT[A/C]TTCTTTATATAAATT | 23072 |
rs190676239 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43265536 | CCTACAAAAATGGCA[A/G]TTTCATAAGGTTCAT | 23072 |
rs190678096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160360 | ATGCTTCACTTGTGT[C/T]GTTGTGGTTTAGTCT | 23072 |
rs190680065 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43197145 | GTGATGTAATCCAAA[A/G]GAGAATTTATAGAAA | 23072 |
rs190682392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141794 | TGAACCACCGCACCC[A/G]GTGAGATATTTGGAT | 23072 |
rs190683073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43322189 | ATTCTGCTGACTCAG[A/C]CTCCCGCGTAGCTGG | 23072 |
rs190691624 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375858 | TGATCAAACCATTGT[A/G]CTCCAGCCTGGGTGA | 23072 |
rs190694012 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | HECW1 | GRCh38.p7 | 7:43184020 | TTTATTATTATTATT[A/T]TTTTTTTTTTTGAGA | 23072 |
rs190694791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43209822 | GCGGGCATTCCAGAA[A/G]AGTGAAGGGAGCATT | 23072 |
rs190696831 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43394067 | GCTTTAGCCATTGAT[A/T]GTTAATTGTCCTGGT | 23072 |
rs190697091 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43177880 | ACTCCCCTACAGGAG[G/T]CACTGTCTCCCTCTT | 23072 |
rs190698931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359494 | GGAAATATTTGCAAT[A/G]TGTAAATCTATTCAG | 23072 |
rs190715624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124342 | CAAATCTGTTTTTTC[A/T]AAGTGCTATTAGCAG | 23072 |
rs190724206 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43450765 | AGTTTTACAGTCATG[A/C]TTTTTTGATGATGTT | 23072 |
rs190727138 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148291 | GGCCTCCACATCCCT[G/T]TCTTTGGATGTGAGT | 23072 |
rs190728803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43412345 | TGCTTTAAGTGGATG[C/T]GTATTTTAAAGAAAC | 23072 |
rs190730969 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43432832 | AATTTCATTAAGTTC[A/C]ATTTATAAAAGTTCT | 23072 |
rs190736464 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126499 | AGTTAAGACAGAGAC[C/T]ATTAGACCCACAAAA | 23072 |
rs190747368 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150709 | AAGATGGCGTCACAA[C/T]GGCAAAGAAACCAGT | 23072 |
rs190757683 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43184393 | TTGGGCAGAGATGCC[C/T]AGTAGCAGACCATTA | 23072 |
rs190762814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43340135 | ATTTTGTTTTAAAAT[C/T]AGCTTACTTAGTTAG | 23072 |
rs190768777 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319008 | TGAAAGTGTGGGGTC[A/T]GGAACCAAGGAGGTG | 23072 |
rs190792585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439488 | CTCCTTCTCTGCCCT[A/G]CTGGCTGCTCTCACA | 23072 |
rs190794838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43474519 | TTATATTAATCAATG[A/G]CAAAATAAAGATATA | 23072 |
rs190821836 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43548288 | TTAATTTTCTAGGTA[G/T]GCAGGTCATCTGCGA | 23072 |
rs190824254 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514459 | ACGCCCAGCTAATTT[G/T]TGTATTTTTAGTAGA | 23072 |
rs190846486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43370831 | TCAGTGGTTGTGAAG[A/G]TTTAGCGGGGAAGGA | 23072 |
rs190863066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43404609 | GTGTATCGAAAAAGA[C/T]TCATTTATATTTGAG | 23072 |
rs190870526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376571 | CACTGAAGGATAAAA[A/G]ATTTCAAATATAGCT | 23072 |
rs190879020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43400550 | AAACTATTCTATTGA[C/G]AGATACCTACTAAAG | 23072 |
rs190887307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43291463 | GGAACGTTCCTGTGA[A/G]CATGTCCTGCACAAA | 23072 |
rs190892781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225253 | TAAAAACAAAGAAGG[A/C]TGGCGATAGCAAGTA | 23072 |
rs190894009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513400 | GGCAAGGCACTGCCC[A/G]AAGACATCAATGGAG | 23072 |
rs190896148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530747 | TCTCCCACCAAGCCA[C/T]TTCTTCCTGTCATCC | 23072 |
rs190901728 | snp | A/G/T | 0.00358938 | 0.0422398 | intron-variant | HECW1 | GRCh38.p7 | 7:43243342 | GGTGACAGTCACTCC[A/G/T]CAGGACAACAAGTGG | 23072 |
rs190911768 | snp | G/T | 0.000171321 | 0.00925371 | intron-variant | HECW1 | GRCh38.p7 | 7:43554574 | TCCTGTCTTCCTCCC[G/T]CCCTTTGCCTCGTGC | 23072 |
rs190917648 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43230142 | TCACGCCTGTAATCC[A/C]AGCACTTGGGGAGAC | 23072 |
rs190919798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43333062 | CATGACTAAGGCAGA[A/G]GATTGGTGCAAAATT | 23072 |
rs190921219 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43262987 | AAGGCTACACATTTG[A/T]ATGTAATAGTTATAT | 23072 |
rs190922956 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43181127 | TGCCTGGCTTATTTC[A/T]CTTAACATAATGTCC | 23072 |
rs190925371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43194141 | GAGGGTATCATGAGG[C/T]GTGTCCCATATGGCC | 23072 |
rs190929666 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43206393 | GCCAAAAAGGTCTAC[C/T]GTGCTTTTTTCTGGT | 23072 |
rs190935231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43270705 | ATATAGCATTTGCAG[A/T]TGTTTAATTATTGAA | 23072 |
rs190944021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43391182 | ATTAAAAGAAGTTAA[C/T]CACTTACATCTTTAG | 23072 |
rs190949161 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43197475 | TGGACAGATGCCCAG[A/G]AGCGTGCACAGTGGC | 23072 |
rs190950032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43438960 | ATCAGAAGGACTTTG[A/G]AATCACGGATAATTA | 23072 |
rs190962142 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43454560 | ATCTCCTAGGACATA[G/T]TTATACAATCTGCCT | 23072 |
rs190963496 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134033 | TATAATTAGTCACAA[A/G]CCCTCTCTAACTTGT | 23072 |
rs190965740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43164974 | GGTTTCTAAAGGTTC[C/T]TCTCTCTCTGAGTCA | 23072 |
rs190975006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43169098 | GGGAAAGAAATCAAA[C/T]GCTCTCCCTCAATTT | 23072 |
rs190976215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43409231 | AAACTTCCTCCTAGC[A/G]TTGGTTATCAACAGA | 23072 |
rs190977152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43494548 | TTGCTCTGTTGCCTG[A/G]GCTGAAGTGAGATGG | 23072 |
rs190979077 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43474183 | GGCCAGGCGCGGTGG[C/T]TCACGCCTGTAATCC | 23072 |
rs190980914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163150 | CTTTTGCTGTATCCC[A/G]TCTGTGCAAACCACT | 23072 |
rs190982344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43429392 | AGCAGCATGGTCTCC[A/G]GCACTTCCTCCCTAG | 23072 |
rs191029775 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127391 | AGCCAGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 23072 |
rs191033243 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454840 | GCTATGGCTTTTCTC[A/C]CTGAAAAGGCTGGAT | 23072 |
rs191055840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518354 | TACAAAAATTAACCA[A/G]GCCTAGTGGCACATG | 23072 |
rs191063398 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494955 | TGCCTTTGTCTTTCC[A/G]GGAATGACTTCCCTA | 23072 |
rs191071085 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43561327 | GAGGAGTCAGACTTG[G/T]CTCCAGAGCACACTT | 23072 |
rs191095620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412113 | GGTACACGGCTTTGC[A/G]TTACTTCCTTTGTAG | 23072 |
rs191095812 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43449813 | GGCCATCCTTTGTCC[C/T]GGGCCCTTCTCACTC | 23072 |
rs191111367 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43420170 | TTGATTTCTTTATTA[C/T]GGCTAGCAGATATTT | 23072 |
rs191117868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119139 | ATCTTATTTGAAGCT[A/G]CTTTTGTGTTTCTGC | 23072 |
rs191142425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43271129 | ATATATATTTCATTC[C/T]AAAATTCCACAAATT | 23072 |
rs191142729 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43240042 | TTAGGAAAAAAAGTT[A/T]TTTTTAAATGTCATC | 23072 |
rs191143185 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43561042 | GTCAGGTGATTCAAG[A/G]CTCCACAGCAGGGAA | 23072 |
rs191147159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510243 | ATGGTAGAGAGTGCT[A/G]TGACCTGTAACACAG | 23072 |
rs191149626 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43527246 | GGAGGGCTATGCTGC[A/G]GGTGGGCACTCCCTC | 23072 |
rs191150437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43266713 | ATATTTTTATTATAC[C/T]GCACACCTCCTTCAA | 23072 |
rs191155382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550149 | AAAAATTAACCAGGC[A/G]GAGTGGGGCTTGTCT | 23072 |
rs191159992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43350247 | GCTGTCAATCTGATA[C/T]GTTTTCCTTTATAGT | 23072 |
rs191163293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43354528 | TGAAGTGAAAAATTT[A/G]TTACACGTTCTCAAC | 23072 |
rs191164613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43259739 | AAGATTAGTGAACTT[A/C]AAGAATGGTTAATAG | 23072 |
rs191166776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43151214 | GGGTGCAGCTGGCTA[C/T]ACCTTTTCTTCCCCA | 23072 |
rs191166986 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43190706 | TGGGGCAGTCTTAAG[G/T]TTTCCAAAAAACCCA | 23072 |
rs191170646 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43203611 | TATAGGCACCTGCCA[C/T]CATACCCGGCTAATT | 23072 |
rs191176385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43375421 | CGATTTCAGGATTGC[A/G]AAAATTGTGGATGGC | 23072 |
rs191178906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43220779 | AGGTTTAGGAAAGCC[A/G]CCAATCCCTTCCACC | 23072 |
rs191182926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118471 | ATATAAGACCTTGCC[A/G]TCAGTGCCGTCAGTA | 23072 |
rs191193962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43233865 | ATAGCAACACAATGG[A/G]CATAATAGAAGCTGT | 23072 |
rs191196404 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43230624 | AATGTCCTGTTTTTA[G/T]GAAATATGCATCATA | 23072 |
rs191197671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43178585 | GTGTTGAGCTCCTCA[A/G]TGCTTATTAGGCACT | 23072 |
rs191199352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134928 | AAAAAATGTATCAGA[A/G]CATTTTGCTAAAATG | 23072 |
rs191199715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161067 | CCTGTGGAGTAAAGC[A/G]GGGCTGGGACCTTTG | 23072 |
rs191199986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43434437 | GTGAATAACAGAGTC[C/T]AGAACTTGGATGTGC | 23072 |
rs191212158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203214 | CAAATAGTTTTATTT[G/T]GCTATATTATCTTTA | 23072 |
rs191217831 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43490097 | CTTTTGAGTCATTAC[A/G]TAATGGATTGCCACC | 23072 |
rs191225306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43469868 | CAGTCATGTCTGTGA[C/T]GTGTCCTTTCCTCTG | 23072 |
rs191229769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286522 | TCATTATAGTAAATA[C/T]TTAAAGGAATATTTA | 23072 |
rs191254372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43176712 | AGTCCTCTTGACCCA[A/C]TCATCTCCCGAAGGT | 23072 |
rs191257088 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111236 | TTTTGTTTTCTTTCA[A/G]GTCTCTGGTTGGAAA | 23072 |
rs191263053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43329931 | TTCTTTTTAATAAGC[A/G]TGCCATGTTATTCTG | 23072 |
rs191263550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144615 | TGAACTTGTCTGGGA[A/G]CCCTTTTATTGACTT | 23072 |
rs191265146 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43309681 | CCCCTGAGCACCAGT[A/G]TATAGAGCACCTTTA | 23072 |
rs191277996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141272 | AGTTGCCTCACCAGG[A/G]TGCCCACCCCCACGG | 23072 |
rs191279000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43558019 | ATTGACAGCAGGGAG[G/T]GTGAAGAATGTCCAT | 23072 |
rs191287162 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43495382 | GTTTTCTGTTCTTAT[A/G]TTAGTTTGCTGAGAA | 23072 |
rs191300916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43538840 | AATTAACCGCGGTGA[C/T]TAGAACTGACAGAAT | 23072 |
rs191311599 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43533143 | ACTACTGGGCATCTA[G/T]TAGGTAGGAGTCAGA | 23072 |
rs191337914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43429232 | GATCAAAATCCAGTT[C/T]ATTTGCTCTTATGCA | 23072 |
rs191367658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43463881 | CCTCCCACCCTGCCT[C/T]ATGGGGAGCAATGTG | 23072 |
rs191384481 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43285272 | GAGCTCTGAAAAACC[A/G]TGATACTCAGACCTC | 23072 |
rs191385129 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43236369 | TCAAAGTGTCTGACA[C/G]AGGTGTCAGTCAATT | 23072 |
rs191386026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523572 | TGAACCCGGGAGGTG[A/G]AGGTTGCAGTGAGCA | 23072 |
rs191388043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43504755 | TCCAACCCTCAGCAC[C/G]CTTCCTCTCTCCTAG | 23072 |
rs191389426 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43355230 | GAGTAAAAAGGAAAC[A/G]TTTGAAGATATAAAA | 23072 |
rs191400811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43393874 | GCTTAGCATGAAATA[A/C]GCCATTTAATCCTAT | 23072 |
rs191408340 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187920 | TCACATGTGCAACCA[C/T]CTGTTACCAAGCAGG | 23072 |
rs191409248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328357 | GACTATTCGTGCAAG[A/G]CAACTTCAGGGAAAC | 23072 |
rs191412112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43390397 | ATTTTTTTAATTTGC[C/T]AGGCATGGTGGTGCA | 23072 |
rs191415248 | snp | C/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359106 | GTTGGGATTACAGGC[C/G]TGAGCCACCGTGCCC | 23072 |
rs191420647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43243748 | TGATTTTTCCTTTTG[C/T]ACGTCGGTTGCCCAG | 23072 |
rs191420962 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43201592 | AGATTTGTGACTTAA[C/G]GTACCCAAGTGGTAA | 23072 |
rs191428823 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43382179 | TAGTCCCAGCTGCTC[A/G]GGAGGCTGAGGCAGG | 23072 |
rs191429835 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43217331 | GCTATGTATAAAATA[C/T]ACTTTGGGTTCCAGC | 23072 |
rs191430620 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43278501 | ATCACAGACCCCAGC[A/G]TGGGCCTTCTCAAAG | 23072 |
rs191433955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156926 | CCTACCCACCCAGAT[A/T]AGACATGTAGTGTGA | 23072 |
rs191436192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138478 | GGAGTTGAGGGTCGC[C/T]TTGGGGGAGTTCATT | 23072 |
rs191438991 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43402353 | TCACTCCGGTTCCTG[C/T]ACCTGCCCGTCTGCA | 23072 |
rs191442939 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43249000 | AGTGTGGTCCAGCAC[C/T]GCCCTGGGTGAGCTG | 23072 |
rs191444422 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43173967 | GTCAGCTTCCCTAGT[A/G]GCTGGGACTACAGGC | 23072 |
rs191447417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43430037 | TAACACAACCCAAAT[C/G]AAATTAACTTTCCTT | 23072 |
rs191451218 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HECW1 | GRCh38.p7 | 7:43366034 | CTTGAACCTGGGAGG[C/T]AGAGGTTGCAGTGAG | 23072 |
rs191451472 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43409448 | TGTTCTAAGACATTT[A/G]GTCATAAAGGTGTTT | 23072 |
rs191455329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43465196 | GCAGAAAGTTTATTT[C/G]TGAGTTTGATATTAA | 23072 |
rs191460348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43243017 | ACTTGTTTCTTACAC[A/G]ACTTCATTTGTCAGC | 23072 |
rs191465092 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43448476 | CAAGTTACCTAGCTG[C/T]TCTGTGCCTCAGTTT | 23072 |
rs191466943 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43323029 | ACCTGACTCAGATTC[A/G]AAGGGCAGTGACCAC | 23072 |
rs191467245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43487392 | TATGATGAAAGCGAT[C/T]GATATCAAAAGAAAA | 23072 |
rs191480060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159969 | CAGGCGTGAGCCACC[A/G]CGCCCAGCTGTATCT | 23072 |
rs191487880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155556 | TTTACTTTGGCAAAA[G/T]AATTTTATATATATG | 23072 |
rs191492166 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43189629 | AACTTGACCTTATTA[A/T]GAAAAATAAATACAT | 23072 |
rs191496367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123513 | CTTCTGGAGCAGGGA[C/G]CACTTTCTGTCTAAA | 23072 |
rs191497057 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43205945 | CTGTCCTTTAGCCCT[A/C]CAAGGAGAAGGTCTT | 23072 |
rs191504500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43187389 | AAAGAATCTGTGGAC[A/G]TATTTTGAACCACCA | 23072 |
rs191536163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514851 | CATACTGAGTTATCC[C/T]ACTTTTACAGATGAG | 23072 |
rs191558801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43556896 | TGGGCTTATGAACAC[A/G]TTCTTCATATCTGAA | 23072 |
rs191580199 | snp | C/G | 0.00408273 | 0.0449966 | missense | HECW1 | GRCh38.p7 | 7:43469021 | CCAGCACAACCGGGA[C/G]TTGGTGAATTTCATC | 23072 |
rs191582523 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43360780 | GTGGCCTGGCTTGCT[C/T]GTGGGGGAATTATGT | 23072 |
rs191590840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43340585 | CTGTCTGGGGGTGGT[A/G]ACAGTAATCAACACT | 23072 |
rs191591789 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43447458 | AAGAAATATCTAAGT[C/T]CCTGAACTCTGCAGA | 23072 |
rs191603508 | snp | A/C/G | 0.000399281 | 0.0141238 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445242 | CTCGTGCTACAGCAC[A/C/G]TCCTGCTACAGCAGC | 23072 |
rs191613352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510150 | GGATGATGGAGCAGA[A/G]CAGACAAGTCACCGT | 23072 |
rs191619667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43550205 | AGGCAGGAGGGTCAT[C/T]TGCCCCCAGGAATGC | 23072 |
rs191621022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43501052 | CACTGAGAATTTGCA[A/G]GCAGCATGTACCTAT | 23072 |
rs191621596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43549630 | AGCCTTCCCTGATGA[C/T]TCAAGCATGTCCTAA | 23072 |
rs191622344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520465 | CTCTGCTGCCCATAT[A/G]TGCGCGATTGTTTCT | 23072 |
rs191629007 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113624 | AGTCATGTCGCCTAC[C/G]GTATTGCGACTTGCA | 23072 |
rs191633050 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260200 | TGGAGGATGTATACA[A/C]CATGCTCTGAGGACA | 23072 |
rs191646123 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247943 | GAAAAAAGAGAGAGA[A/G]AAAAGGAGGGAAGGA | 23072 |
rs191656342 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43427266 | ACACAACACACAGAG[C/G]GAGGTGCCACAGTCA | 23072 |
rs191661180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43321529 | CACAGCTTACCTTCA[G/T]TCCACAGCTCCTTCT | 23072 |
rs191661669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300064 | CTTTGTCTTTGCCTC[A/G]TTGTGATTTCTTTCT | 23072 |
rs191666673 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43409145 | CTGGGCTTAATTAGC[A/G]CTCTCCCAGGCTTCC | 23072 |
rs191668320 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43240179 | AACCCCATCTCTACT[A/G]AAAATACAAAAAGCC | 23072 |
rs191668415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43407120 | CTGCCCTCCCTGGCA[G/T]CAGGGTTTCTCAGAA | 23072 |
rs191676191 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | HECW1 | GRCh38.p7 | 7:43275708 | TGTTCTTATGCGCAC[A/G]CACACACACACACAC | 23072 |
rs191677185 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43460815 | CATGACCTGCTTCCC[C/G]AAACTGCCTCTGTGC | 23072 |
rs191677991 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43371041 | TACAGGTGCCCGCCA[C/T]CACGTCTGGCTAATT | 23072 |
rs191690446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43528495 | ATGGGTCAAAAAATA[C/T]CACACTTTCGAATGA | 23072 |
rs191690596 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43483901 | AGAAGAGGAAGGGCT[A/G]TGGCAAAGAGCTATT | 23072 |
rs191693699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43262567 | CTTCAAATGAATCTA[C/T]AATTACTTACTTAGC | 23072 |
rs191694927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43326872 | ATGTTTCCCTGCGGC[A/G]AAGCAGCCAGAGCCA | 23072 |
rs191702294 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43258479 | GCGTGCCAATAAAGC[A/G]ACTGAGAGGCGTATG | 23072 |
rs191724208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43388299 | GTTATTATGCAATAC[A/G]ATAATGGCCAACATC | 23072 |
rs191724924 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302607 | CACAAATGCCCGGTA[C/T]GGGGCCGCCCCGGGA | 23072 |
rs191732826 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298138 | TGTGCCCTGGTACCT[G/T]TATATTCTAGTTGGA | 23072 |
rs191737602 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43192874 | AGGACTTCAAGAGCC[G/T]GCTCACAGGGTAAAG | 23072 |
rs191740287 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43190195 | CTCGGCCCACTGCAA[C/T]CTCCACCTCCTGGGT | 23072 |
rs191741495 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43172777 | GAATACCTGATATTG[A/G]GAAATACTCTTATTT | 23072 |
rs191756936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43220339 | AGCACAGAGTATTGC[C/T]AGTAGAGACACTCGC | 23072 |
rs191761933 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43224843 | AGAAAAAGGACCCAC[A/G]TAGGAAGTGTCTCTG | 23072 |
rs191794435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43475594 | CTCGCTCTGTGTCCT[A/G]GGCTGAAATGCAGTG | 23072 |
rs191798880 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133445 | AATTCATTAATCTTA[C/T]GGTTATTGGTCTCTT | 23072 |
rs191801898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43168938 | ATAGAAAGATATGCA[C/T]CAAACTGATAATAAA | 23072 |
rs191811396 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43169680 | TTATCTTTGTATCTT[C/T]TTTTCTTTTCTTTTT | 23072 |
rs191820731 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43184066 | TTGCCCAGGCTGGAT[C/T]GCAGTGGCTAGATCT | 23072 |
rs191823826 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198109 | CATTCACACACTCAC[C/T]CTACACATACCCACT | 23072 |
rs191827223 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134298 | ACTTGGGAGGCTGAA[A/G]CAGAAGAACCGCTTG | 23072 |
rs191828848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43547504 | GCAAGCCAGGATTGC[A/G]CCACTGCACTCCAGC | 23072 |
rs191834023 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116974 | GCAATATGTAGAGAA[G/T]AAATAATTAAGGCTA | 23072 |
rs191837213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148667 | ATCAAATAAGAAAAG[A/T]AGAGTGCATTGGGAG | 23072 |
rs191839083 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43401039 | GTTGCACTCACCTGG[A/G]CAGTCCAGGATAAAT | 23072 |
rs191842117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43356898 | ACTCAAGAGCAAAAA[A/G]CAATCTGATTTTTAA | 23072 |
rs191849772 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43420442 | ACTTTAGCCACTTCT[C/G]TTTAATATTGTGCTA | 23072 |
rs191853470 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43486503 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 23072 |
rs191857072 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43380631 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 23072 |
rs191857288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43336625 | GCATAATAATGAGGA[C/T]TGGGCTTCTAATCTA | 23072 |
rs191864305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439801 | AAGCAAGTACCTGAG[G/T]TGGAAAAGGGTGTCC | 23072 |
rs191869066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522952 | TATTGCTGGCACTTC[C/T]GCCTACTCTTTGTAC | 23072 |
rs191873203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43455251 | CTAGTTACTGGTTTC[A/G]TTTGGTGGCCAGAGA | 23072 |
rs191882243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256327 | AGTAAAGATGAACAT[C/T]GGCTGGGTACGGTGG | 23072 |
rs191883197 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43505074 | TCCCTGGCCATTCCC[A/G]CAGCCTCATCCTCCC | 23072 |
rs191883981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43419843 | GCCACGAGAGTACGC[C/T]GAACAAAGGAGACAA | 23072 |
rs191893318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523755 | GCAAGAACCAGAGGG[A/G]GGGAGAGGCTGGTGA | 23072 |
rs191893991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43489780 | TGGAAGTGGGAACCA[A/G]AGGAAAATCAGCAAT | 23072 |
rs191905323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43315784 | CAGGCGTGATCCACC[A/G]CGCCTGGCCCTGTCC | 23072 |
rs191908468 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43526154 | TTAAATAGCTTCAGG[C/T]ATTTCTGGTATCCTG | 23072 |
rs191913395 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43364763 | ATCTTCCTGTTTTTC[A/T]TACTTTTTGTGTCTT | 23072 |
rs191914545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43447844 | GAAACTGCATTAGAC[A/G]GCTGGGTGTGTGGGC | 23072 |
rs191920178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43294536 | CTGGATGCAGTCAGA[A/G]AAAAGCAGATTATTC | 23072 |
rs191926080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43273212 | GTTGAAAAACTAATT[G/T]CTGGGTACAATGCTC | 23072 |
rs191938621 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303034 | AAATATTATGAACAG[G/T]AATTTGCCCCAGCTA | 23072 |
rs191955573 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43379942 | CAGAGCTGTTCCTTA[C/T]CACCCACCAGAGCAG | 23072 |
rs191963862 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43343964 | CTAACTGGTGTGAGA[C/T]GGTGTCTCATTGTGG | 23072 |
rs191984555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43274662 | GAGAGAGAGAGAGAG[A/C]GCGAGAGAGAGCGCG | 23072 |
rs191992885 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43233284 | CCAACTAACATAATT[C/T]ATTTAGTCTCCAGGA | 23072 |
rs192006103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145545 | TCAAGCAATCCTCCC[A/G]CTTTGGCCTCCCAAA | 23072 |
rs192009024 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43170862 | GAGCTGAAAGTAGGG[C/T]GGAGCAGCACATGTG | 23072 |
rs192011921 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43239442 | GTTGGTTGGTCTGTC[A/G]GCAAATAGTTATTAG | 23072 |
rs192023322 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43199481 | TCCCCCTGGAACTTA[C/T]ATTTCTATTTCACCA | 23072 |
rs192035127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43181856 | GCAGTGGTGCGATCT[C/T]CACTCACTGCAAGCT | 23072 |
rs192037227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43166557 | TTTTAAGAAAAGATA[A/G]GGGTTAGTCACATTA | 23072 |
rs192041201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203387 | TTCTTCGATTATTTT[G/T]TAAAGATAATTCCTG | 23072 |
rs192054797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43194974 | GCTGGGATTACAGGC[A/G]TGAGCGCCCGCTACC | 23072 |
rs192060918 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130837 | AGTATTTCAGATTTC[A/T]GATTTTTGGATTAGA | 23072 |
rs192067130 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43564110 | AATAATGGATTCCAA[C/T]GGAGCTATTGTTTTA | 23072 |
rs192070374 | snp | C/T | 0.00275839 | 0.0370349 | intron-variant, utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114304 | AACCGTTAAAGACCC[C/T]GGCAGTGTTGTGGTC | 23072 |
rs192081823 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146291 | GATATTTGGCAGCAT[C/G/T]TCTGGCTTCTGCTTG | 23072 |
rs192092374 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147764 | GAGAGTTTCAGCTGC[A/G]AAGGGACTGGCCATT | 23072 |
rs192096764 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43396137 | ACCTTCCTAGAAGAG[A/G]ATGGAAGCAAAAACC | 23072 |
rs192103899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43417090 | AGTTTCACTCTGGTC[A/G]CCCAGGCTGGAGTGC | 23072 |
rs192104448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43394825 | TGCTGTGCGGGAGAC[C/T]GGAGTTTATTATTAC | 23072 |
rs192108741 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43458375 | CCATGAAAGTTTATC[A/G]GGGTGATCTGCTTGC | 23072 |
rs192109363 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43378030 | ACACATAGTCACTAA[C/T]AAATAGTTGTGTTTT | 23072 |
rs192111579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43498070 | TAGATGGCTTCCTCA[A/G]TTCTCAGTGCACTTT | 23072 |
rs192128520 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43435784 | TTAGTGCAGCATGCC[A/C]TAGCTCATCCTGACT | 23072 |
rs192129567 | snp | A/C | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115845 | TTGTTCATAGAGCTA[A/C]GATAGCACTTACAAT | 23072 |
rs192132003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43537806 | TTTTTTAAAAAAGCT[A/G]TGGCTTGTTTGTTGC | 23072 |
rs192138655 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43471137 | TCTCTTAATGTCCCC[A/C]AAAATAATCCAAGAT | 23072 |
rs192142815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43452403 | TATAAGCCACTTTCA[A/G]TAATGAGAACAAATT | 23072 |
rs192145641 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43464353 | TGGGAGTGAAGAGGT[G/T]TTCCAGCATGCCACA | 23072 |
rs192150470 | snp | C/T | 1.70351e-05 | 0.00291843 | intron-variant | HECW1 | GRCh38.p7 | 7:43542017 | TGTGTGACATGGGGT[C/T]TGGAAAAGGGATTTT | 23072 |
rs192152651 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43504415 | TCACGGACTTTTCTC[C/T]TTTCCTTTCTAACGT | 23072 |
rs192157337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43275181 | TATCTTTAAAAATCC[A/G]ACAAAAAGTTTACTT | 23072 |
rs192166295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43250672 | GTCTCTCTGAACTTG[C/T]GTAAAAAAATAGCCC | 23072 |
rs192174736 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43544892 | TAAATTGGCATGAAA[A/T]ATGTCTAAGATATAG | 23072 |
rs192182566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43361410 | AGTAGGATTTATTGC[C/T]TCAGGTTGATTTTAG | 23072 |
rs192192220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43341018 | TTTGCAGGGACTTGG[A/G]TGAAGCTGGAAAACA | 23072 |
rs192195546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43211829 | TTTCTGCCTTGTACA[A/C]CTCAGTTAAGAATAA | 23072 |
rs192201746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43399461 | AAAACAGTAGAAACC[A/G]GGAATACTGCACAAC | 23072 |
rs192220348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184541 | TGGCTGGTGGCTGGA[C/T]GTCCCTAGATAGCTT | 23072 |
rs192235722 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43308818 | GTAGAGACGGGGCTT[C/T]GCCACGTTGGCCAGG | 23072 |
rs192241831 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43323583 | GAACTCCAGCCTGGG[C/T]GGCAGAATGAGACCC | 23072 |
rs192257552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124865 | AATGATTTTACAATA[C/T]TCAGTGGGCCAAACC | 23072 |
rs192263050 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250246 | GGTCACTCTGGTCCA[C/T]AGCAGCCTCATGAAC | 23072 |
rs192264380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43278930 | TCCTCCCCATTAGGA[C/T]TCAAGCTCTGTGAGG | 23072 |
rs192270511 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363709 | TTAGGTTTCATAGGA[A/G]CCACTGGGAGGAGCC | 23072 |
rs192274008 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43478001 | TCTTATGGTACAAAG[A/G]GTTTTGTTGAAAAAA | 23072 |
rs192286628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43198364 | TAGTCACACACCCCA[C/T]GCTCTCACACACACG | 23072 |
rs192288391 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43286062 | ATCAGAGAGACCTTC[A/G]AGCCATGTCCAAGAT | 23072 |
rs192289556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43211080 | GGCTATTTCTTTACC[G/T]CCTATTTTTGCCTAA | 23072 |
rs192290193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43546025 | TCAAACAATCAGAAC[C/T]GTTCTGCCAGATTGT | 23072 |
rs192295169 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43267802 | ATGTTCAGAATTTTA[A/G]TAATATATTTGAAAG | 23072 |
rs192296173 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516070 | TAGTGCATCCATTTA[G/T]AATTTTCCAACTTAA | 23072 |
rs192296734 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43191719 | AAACCACTTGCTAAC[A/T]CACTATGTATGCTTT | 23072 |
rs192300008 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43533984 | AGAAGGTCACCCAAA[A/G]CAGGAGACCCCTTGA | 23072 |
rs192302119 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43231742 | CCTCTTGGGGCCAGG[C/T]GCGGTGGCTCACGCC | 23072 |
rs192310501 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43557679 | GTTAGAAGTTCAGAG[C/G]GTCAGAAGGAACCAA | 23072 |
rs192318973 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214005 | TATAAGACCTTTAGA[A/G/T]ACCTTTATTTTAATT | 23072 |
rs192338176 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43252809 | TACTGGGGGAAAGTA[G/T]TCTTGCAGTGTAGTT | 23072 |
rs192355744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43185599 | GGTGGGGAAAAATCC[A/G]CACACATTTTGGTGG | 23072 |
rs192365127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43455712 | ACCATCACACCATCA[C/T]GGGTGTGATGACCCG | 23072 |
rs192366319 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43442019 | GATCTTTTCCTTGGC[A/T]AGCGATACACAACAC | 23072 |
rs192376884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43335680 | ATATTTGGAATCTTT[A/C]TTTCTTTTTCCTTCC | 23072 |
rs192382564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43477148 | TATTTACCATTTAAC[A/T]TTTCTAAGAGTTCTT | 23072 |
rs192386160 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43293991 | TGAGAACATAAGTAA[C/T]GCCTGATAATCTGAG | 23072 |
rs192386988 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128834 | ACTTTGGAAGACATT[G/T]GTTGCAACCCTCATG | 23072 |
rs192390874 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43496128 | GGGATTGTACAATTA[C/T]GATTTTGCAGAGCTG | 23072 |
rs192393411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515169 | AGCATTCACAGCAGA[A/T]GTCAGTTTGGTGTGG | 23072 |
rs192395035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43372229 | TTATTTCCAGGAAAG[C/G]ATAACAAGAAATGAG | 23072 |
rs192399402 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154021 | CTTGTTACTCAAATT[C/T]CATGTCAGTTCTAAT | 23072 |
rs192433211 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43255969 | TGCTTCCAAGAAAAT[A/C]TGACCTAATTATTTA | 23072 |
rs192452057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225826 | GTCTCACTGTGTCAC[C/T]GAGGCTGGAATGCAG | 23072 |
rs192454886 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43355787 | TGAGGTCAAGAGATC[A/G]AGACCATCCTGGCCA | 23072 |
rs192459368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43371751 | GATGATACACTCTAA[C/T]GGCAAAAGCAGCAGG | 23072 |
rs192459392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43306550 | TATAACCTCATCTTA[C/T]ATACTTTAATGAAGC | 23072 |
rs192462264 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43443262 | AGGACCTCCTGGACC[A/G]TTTACAAGTTGCTGT | 23072 |
rs192477045 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43480238 | ATTCGCGCTCTACAA[A/C/T]GTGCTCTTTCCTTGG | 23072 |
rs192481048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244619 | TCCCCATTTGATGTA[C/T]GAGGGAACTGGGTCA | 23072 |
rs192489256 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43194446 | GCTCTTTTAGAATTT[G/T]TCTAGCAGGTTTTCC | 23072 |
rs192500738 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43334084 | AGTGTTTCAGCCAAG[A/T]CAATGGTTGTGCATA | 23072 |
rs192504460 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518198 | CAACAACTAGAATCT[A/G]TAAAAGAAAAGAAAG | 23072 |
rs192505968 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129636 | TGAAAAACAAAAACA[A/C]AACGGATAAAGGACA | 23072 |
rs192506765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43281187 | TCCCTTCAGCAGCCT[C/T]TGGCCCTGTCACTGC | 23072 |
rs192507564 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43208173 | TCCAGATCTTTACCT[A/C]TTCATGTGACATCTG | 23072 |
rs192510738 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43166123 | GAGTTTCACTCTTTC[A/G]CCCAGGCTGGAGTGA | 23072 |
rs192511433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43264611 | AGCACTTTGGGAGGC[C/G]AAGGCGGGCAGATCA | 23072 |
rs192512528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43315135 | CTGACATAAGAGGGG[A/G]AAGATACCTGGATGT | 23072 |
rs192512848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43227761 | AAATAAGATTAATAC[A/G]ACTGTATTTTAAAGC | 23072 |
rs192522946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268715 | CATGTGCCTCAGGCA[C/T]GACAAACTCCAAATG | 23072 |
rs192525917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156538 | AAATGATGTGTATCT[A/G]TTTCTATGTTTGGCT | 23072 |
rs192527774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299011 | ATCATTGAGACTTCT[C/G]AGTTTCTATTAGTCT | 23072 |
rs192533316 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43196102 | TCTTTTTGCTAGTCA[A/T]GTGAAACTGCCGCCT | 23072 |
rs192534840 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43182076 | GGCGTGAGCCACCGC[A/G]CCAGGCCTCTCATAT | 23072 |
rs192548688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563391 | CTGAAATAGGTCATA[A/C]ATGAAAGTGTTTTTC | 23072 |
rs192553990 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43529502 | CAGAAAGTGCCACAG[C/G]AAAGCTCACCAGTCC | 23072 |
rs192567782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137790 | CCTGAGCTCAAGTGA[A/T]CTGCCTGCTTTGGCC | 23072 |
rs192568048 | snp | C/T | 3.31214e-05 | 0.00406935 | missense | HECW1 | GRCh38.p7 | 7:43552289 | TGATAGCTGGCACCG[C/T]GGAAATCGACCTAAA | 23072 |
rs192573678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120943 | AGGTGTGAGCCACCA[C/T]GCCTGGGCAGATAAA | 23072 |
rs192575190 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43451903 | GCCTGTGCTTACATG[A/C]AGCAGTTACAGTTTT | 23072 |
rs192576752 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43198742 | TCTCACACCCCACAC[C/T]CTCACACACTATAGA | 23072 |
rs192599682 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43231877 | AAAAAAAAAAATTAG[C/G/T]CAGGCGTGGTGGCGG | 23072 |
rs192606877 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43491042 | ACAGGTGTGAGCCAC[C/T]GCACTGGCAAAATTG | 23072 |
rs192622549 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43453468 | TTTTGATGGGAAGGA[G/T]CCAACACTTGGTTTC | 23072 |
rs192626621 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43170274 | TATATACATGTATAT[A/G]CATTATATATTACAA | 23072 |
rs192635142 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43491753 | ATCTGCCACCACATC[G/T]GGCTAAGTTTTGTAT | 23072 |
rs192635498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377300 | AGTTCAGGTCGATGA[A/G]CAAATGGATTAACTA | 23072 |
rs192635523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43311036 | CTCTGCATCAGGTTG[C/G]CTCATTTTAAGTGCT | 23072 |
rs192636471 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43472124 | CATAGGGATAAAACA[C/G]AGCAGCACTGATGCT | 23072 |
rs192641437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43387559 | AAATGCTAACAGCAG[A/C]AAGACATTTACATAG | 23072 |
rs192642389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142421 | TCTAGCATGCTGAAG[A/G]GTAGCACTGGAGACC | 23072 |
rs192648465 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416893 | GCTTCGGCTCGAGCA[C/T]GGTGTGCGCACCCAC | 23072 |
rs192650865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512059 | GCGTAGCTGCTGCTG[A/C]TCTCGGGTCGGTGTC | 23072 |
rs192657964 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43352739 | GGCTAATAATGATTG[A/G/T]CTATACATCATAGGA | 23072 |
rs192666846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351799 | TTAGAATGATGCTAC[C/T]TTCCTCCTGAGGGGT | 23072 |
rs192668410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369703 | AGAAAAAAGAGGACG[A/T]GAAAATTAAATGAGG | 23072 |
rs192687926 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43456668 | TTAAGGATGGGAAAT[C/G]GTCTAAACTTCTTAA | 23072 |
rs192689234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43406317 | TTGGTTTCTCAACTC[C/G]TTTGGCATTTGGTGG | 23072 |
rs192700936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43496338 | CCCTAAGGAAACTGT[A/G]GACCCAGGTTGAGAA | 23072 |
rs192706530 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43534332 | ACAAAAACTGCTTTC[A/G]TTTAAATAATCTGTT | 23072 |
rs192711029 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43179045 | TAGAAGTGCCAGGCC[C/G]TTCACAAGTAACACC | 23072 |
rs192720466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43391362 | CTGTATCTCATTATT[A/G]GGCCACGAGAAATAG | 23072 |
rs192724323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203902 | CTGACAATTCTTGCT[A/G]TTATGTAATATCTTG | 23072 |
rs192725819 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142723 | TGGAGGATCTAGCAT[A/G]TATACACATTGGTTC | 23072 |
rs192738872 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43423205 | GTGAGTGTGTGAGCA[A/G]CCCTAAAGACGGCAT | 23072 |
rs192764116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43356506 | GCCATATCATTCCAG[C/T]AAGGAAATGTAAATA | 23072 |
rs192766946 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43465880 | GCCTGGATGACAGAG[C/T]GAGACGCTGTCTCAA | 23072 |
rs192779415 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43272554 | AAGACATATAAGCAG[C/G]CAGCAAACATATGAA | 23072 |
rs192795973 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43181468 | TCCACCAACATTGCA[C/T]AAGGGTTTCTTTTTC | 23072 |
rs192798596 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43430524 | AAGGAGGAAGTATTT[C/T]GACTTTTCCCATGAT | 23072 |
rs192799558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43392005 | AGATCTCTGATGCAA[A/T]GTGGAACTCGTAATT | 23072 |
rs192800039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206553 | TTCATTTTTTAAGAG[C/G]CGTAATTAACTTTAT | 23072 |
rs192808952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43280494 | CCAGGCCACTGAGAC[A/G]TAAGACAAGTTTTGC | 23072 |
rs192811452 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121367 | CAAAGCTCTCAGGAG[C/T]GGCCAAAGTACGCAC | 23072 |
rs192813187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145849 | AAAAAAAAATAATAA[C/T]AACAGAGTGGAAGTT | 23072 |
rs192821669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43541318 | GCAGGGCAAGGACAC[C/T]GACCTCTCTGGTGCC | 23072 |
rs192828266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43324515 | ATTGGCTCTACGAAA[C/G]GTTCTCATATGGCTA | 23072 |
rs192831345 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43207444 | AGCATATTTGCCATC[A/T]CAAACATTCATCATT | 23072 |
rs192838415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43243805 | AAACAATGTTGTTTG[C/T]GTGGGTAATGTTGCT | 23072 |
rs192845268 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43435260 | TATAATACACTCCAG[A/C]ATGGAATAACTGGAC | 23072 |
rs192853519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511139 | ATCCCTGATGAGGGC[C/T]TGACAGTGCCTGTCC | 23072 |
rs192865848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43330815 | GGAAAAAGCTCAGGC[A/G]TGAACATGCTGGAGT | 23072 |
rs192867318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119930 | CCCATCTGCAGTCTG[C/T]TCCCTATACAGCAGC | 23072 |
rs192879034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43370028 | AAATGCAACGGCCAA[C/T]AAACACACAAAAGAT | 23072 |
rs192885449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43395194 | AATCTTGCAGCTAAC[A/G]TTAGTCCTACAAAGA | 23072 |
rs192886692 | snp | A/C/G | 0.0681886 | 0.171594 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511797 | GCCCCTGAGTGGCTC[A/C/G]TTAAGCTCTTTGGCC | 23072 |
rs192895665 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43551805 | TTTCTCACAGTTTTG[A/G]AGGCTAGGAAGTCCA | 23072 |
rs192902975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43221941 | GAGATGCAGATCCTC[A/G]TTACTCAAAATGTAG | 23072 |
rs192916900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191331 | CTAGCTCTATTACAG[C/T]GATGTAGCCAGCCTA | 23072 |
rs192929034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300308 | CAGCCTGGTGTGGCT[A/G]AGGCGTGTGGCAGCC | 23072 |
rs192930233 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125386 | GACTTGCTCTGAGTC[A/C/T]AGAATGAAAAGTAGC | 23072 |
rs192932466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161628 | ATGCAGCCTTGTGAG[A/T]TAGTGAACTCTCCAT | 23072 |
rs192936900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328931 | CTGTCTCTCTTAGCC[A/C]TATTGTGCTGGAGGC | 23072 |
rs192939205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43260900 | CATTCACATAGTGCC[A/T]ATTGTGTGCCAAGCA | 23072 |
rs192946068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405356 | CTCAGCATCTAGATA[C/T]ACTCGTGGTATGACT | 23072 |
rs192948126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369132 | TGGACTTCTGTCACA[A/G]GAAATATAAATGTCA | 23072 |
rs192956215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43222864 | CCACTCCCTGCCCTG[A/G]TCATCCCATCCCATC | 23072 |
rs192964250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43449012 | TTGCATTTGCTTGGG[C/G]TTCACAAGCAGGTGG | 23072 |
rs192970353 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43488187 | TGGTGGTGCATGCCT[A/G]TAATCCCAACTACTC | 23072 |
rs192978653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43169976 | TTGTCTGCCAACATC[A/G]TCTTTATCAGAACCG | 23072 |
rs192992697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43373171 | CTCTGTGGTGCTGCC[C/T]ATGCACGTTGGTGTC | 23072 |
rs192999506 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134342 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCATTG | 23072 |
rs193000692 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43410031 | TGAGTGAGCCCCCAG[A/G]GATCCCAGCTCTCCG | 23072 |
rs193007674 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488374 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 23072 |
rs193011320 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43305839 | GATCTCGGCTCACTG[C/T]AACCTCTGCCTCCTG | 23072 |
rs193013392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43524648 | ACATTATTATCCCTT[A/C]TTTGTAGATGGGAAG | 23072 |
rs193021487 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43264467 | CATTTTCTATGTATA[A/C]CACACTGACTTTAGC | 23072 |
rs193026340 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43346312 | TTGAGAATTGTCTAT[G/T]CACGTCCTTAGCCCA | 23072 |
rs193034780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43421888 | AAGCCAGGTGGGAAA[C/T]GAGGAAGCCTGGACC | 23072 |
rs193040273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43226624 | TGTGTCGTTCCAGAT[C/T]CTTGACGAAGCGGGT | 23072 |
rs193058578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43346650 | TAAGTCCTTAATATA[A/T]CTTGAGTTGATTTTT | 23072 |
rs193074903 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43381039 | GTTGTGAAAGGGTAT[A/G]TAGTAGTATTGCAGT | 23072 |
rs193080943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43271518 | AGCAAGGTTGTAGGG[C/T]ACAAAATCAATGGAC | 23072 |
rs193082608 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137619 | CAGTGGTACAATCAC[G/T]GCTCACTGCAACCCA | 23072 |
rs193084889 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43491390 | TGAATGCAATAACAG[C/G]CATTCAAGAAAGAAT | 23072 |
rs193089432 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43236071 | GAGGTACCTGTGCTA[C/T]CCAATGTGATATATA | 23072 |
rs193100489 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43200617 | ACACAGAGCTTTGCC[A/G]TGTTCTCTTGTCTGA | 23072 |
rs193104606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529010 | CAGTATCTGAATAAA[G/T]GTGGGTGTAGAGAAT | 23072 |
rs193109665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146565 | TTGGACCTGGAAATT[C/T]GAGTCTTAATAAGTT | 23072 |
rs193110991 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43173584 | TTCTCATAAGGAGCA[C/T]GCAACCTAGATCCCT | 23072 |
rs193125597 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43436953 | CACTGCAACCTCCAC[C/G]TCCCAGGTTCAAGCA | 23072 |
rs193126570 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43460544 | TGTGCGCGCGTGCGT[G/T]TGTGTGCGTGTGTGC | 23072 |
rs193128887 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43500337 | ACTCCTGATCTCGTG[A/G]TCTGCCTGCCTCAGC | 23072 |
rs193136036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43540900 | GTCCTCATTCTCCAC[A/G]GTCTGAAAAAGGTTC | 23072 |
rs193152306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43426488 | TGGCCTGGAAGACAT[A/G]TTTTAGTATTTTTCA | 23072 |
rs193159197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425633 | CACAGTTCTGGAAGC[C/T]GGGAAGTCCAGTAGC | 23072 |
rs193169598 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43351089 | ACTGTCCCCTTTTCC[A/T]ACGGTGTGGCTTCCT | 23072 |
rs193170474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43276034 | ATAAGGAGGTTTAAA[A/G]AATCAATTGTGCAGA | 23072 |
rs193173787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43385912 | TTGCAAGGTAAAATA[C/T]CTGAAATCAATGTCA | 23072 |
rs193178285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43321913 | CCCCGCTCCCGGCAA[C/T]GACACCAATAGCTCT | 23072 |
rs193180361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43204500 | TAAATATCTACTGAA[A/C]ACCTTGACTCTGGTG | 23072 |
rs193184094 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43240636 | GTTCATTTGATTTTT[A/G]ATAATCCTAACTCTA | 23072 |
rs193194116 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150037 | ATATCTTCTTGCAGT[A/G]CAATATATCTTATGG | 23072 |
rs193195315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43184234 | TAGCCAGGATGATCT[C/T]GATCTCCTGACCTCG | 23072 |
rs193199377 | snp | A/C | | | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117427 | TACACTGCCACCCCC[A/C]ACCCGCCCCACCAAA | 23072 |
rs193208788 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43506696 | GGAGGCCTAGGTGGG[C/T]GGATCACTTGAGGTC | 23072 |
rs193210853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43548128 | TCTAAGTGTTTGTGT[A/G]TGTACATTTTCATAA | 23072 |
rs193222418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43440262 | CGTGGTTTCTGAAAC[A/G]TTTGGCTCCACCTGT | 23072 |
rs193232980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43325467 | TGATCCTGAAAAGAA[A/G]GTATCCTGTCTTGAT | 23072 |
rs193239054 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43365299 | CCTCCCTACAGAGCG[C/T]TCACCTGGCAGTGCA | 23072 |
rs193249727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43255364 | AGCACTTTTGGAGGC[C/T]GAGGTGGGTGGATCA | 23072 |
rs193253225 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293331 | ATACAGAATCTTCTT[C/G]GGTTCAAATACCCCC | 23072 |
rs193257702 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43216424 | GCTGGGATTACAGGT[A/G]TGTGCCACCGCATGC | 23072 |
rs193264464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43187641 | GGGCTTTTCCTTTAT[A/G]TTATAATTTTCTTTT | 23072 |
rs193279169 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43483417 | CATTTCCACACACCC[A/G]TAGATGGTAGCATTA | 23072 |
rs193281532 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43417620 | ACAATCCCAGCTACT[C/T]GGGAGGCTGCGGTGG | 23072 |
rs193284564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519860 | TATGTAGCTAGAGAT[A/T]TGTAAATATAAATAT | 23072 |
rs193290357 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562676 | AGGAGGGGGAGCATC[C/T]CTAGTGAATACTCAC | 23072 |
rs193301136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43445735 | GTGTATCTGTGTATG[A/G]GCATAGATGACTGTG | 23072 |
rs199500629 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43229632 | GAACCTAAAATAAAA[G/T]TTAAAAAAAAAATTA | 23072 |
rs199501571 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192969 | CCAAGGGCTGCTGGC[G/T]GGCTGTTTTTATGGC | 23072 |
rs199504701 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237077 | AGGAGAAGGAGGGAG[-/C]GGAGGGAGGAAGCAG | 23072 |
rs199506289 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248006 | AGGAAGGAAGGAAAG[-/AA]AGAGAGAAAGAAGAA | 23072 |
rs199509786 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179583 | TGTTGTTGTTGTTGT[C/T]GTTTTTGCTGAGACA | 23072 |
rs199510892 | in-del | -/TTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308039 | ATATTATATATTATA[-/TTG]TATTATATATAATAC | 23072 |
rs199530198 | in-del | -/TC | 0.131723 | 0.220251 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132522 | GAACAAGAGTTTCCT[-/TC]TCTCTCTCTCTCTTT | 23072 |
rs199531295 | in-del | -/G | | | intron-variant, upstream-variant-2KB, frameshift-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43113672 | CTGCCGGGGCGGGGA[-/G]GGGGGGGGAATGCGT | 23072 |
rs199539665 | in-del | -/GAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43257856 | TAGAAATAAGAAGAA[-/GAA]TAGTGGTATTCAGTG | 23072 |
rs199542586 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510246 | GTAGAGAGTGCTATG[-/A]CCTGTAACACAGGAA | 23072 |
rs199548805 | in-del | -/CA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544591 | ATGCCTTTGACTCAG[-/CA]CACACGTCTAGAAAT | 23072 |
rs199564649 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480659 | TGTGTGTGTGTGTGT[A/G]TATATATACACACAC | 23072 |
rs199577792 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487206 | ATTAACCCAAATTCA[A/G]TCTAAAACATGCAAT | 23072 |
rs199580832 | in-del | -/CG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480682 | ACACACACATATATA[-/CG]CATATATATATATAC | 23072 |
rs199589167 | snp | C/T | 0.000185624 | 0.00963212 | intron-variant | HECW1 | GRCh38.p7 | 7:43493198 | AAGCCTCGCCCCTCA[C/T]TCCCTGGAACTCTAG | 23072 |
rs199595771 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546094 | TCTTCTTCCCCTTCT[G/T]AACCTGGCACTGGTT | 23072 |
rs199596402 | snp | C/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336162 | TCTCTCTCTCTCTCT[C/G/T]TCTCTCTCTCTCTCT | 23072 |
rs199597438 | snp | A/G | 9.94085e-05 | 0.00704942 | intron-variant, missense | HECW1 | GRCh38.p7 | 7:43450839 | GTAGGTGAATGTCCT[A/G]TACTCCATAATTCCC | 23072 |
rs199600516 | in-del | -/GTCCC | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125877 | ATGGAGGCTGGTCCT[-/GTCCC]ATCCTGGAGAAGTGA | 23072 |
rs199600642 | in-del | -/ACTTTTT | 0.0126979 | 0.078662 | intron-variant | HECW1 | GRCh38.p7 | 7:43291669 | AACTTTGAAGAGGAA[-/ACTTTTT]ACTTTTTACTTTCTA | 23072 |
rs199600897 | in-del | -/TTG | 0.0427531 | 0.139817 | intron-variant | HECW1 | GRCh38.p7 | 7:43305586 | AAACTGGATAGTGTT[-/TTG]TTGTTGTTGTTGTTG | 23072 |
rs199602932 | snp | G/T | 0.000216207 | 0.010395 | intron-variant | HECW1 | GRCh38.p7 | 7:43450796 | GCCACGGCAGTGAAT[G/T]AATCTGAATGTATTG | 23072 |
rs199617441 | in-del | -/GA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43550114 | TCTACCAAAAAAAAA[-/GA]AGAAGAAGAAGAAAG | 23072 |
rs199623088 | snp | A/G | 1.68917e-05 | 0.00290613 | intron-variant | HECW1 | GRCh38.p7 | 7:43407741 | GCCGAGGTGAGTGCT[A/G]TGGGCCCTGAAAAAA | 23072 |
rs199623825 | in-del | -/AGCAAGAAAGGGAGGGAGAGAGGAAGGAA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247875 | AGAAAGAAGAAAGCA[lengthTooLong]GGAAGGAGGGAGGAA | 23072 |
rs199626474 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43393678 | TCTTTTTTCTTCTTC[-/T]TTTTTTTTTTTCATC | 23072 |
rs199648071 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43186499 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 23072 |
rs199663227 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43417247 | GTAGAGATGGGTTTC[A/G]CCATGTTGGCCAGGC | 23072 |
rs199672684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127383 | ACAAAATTAGCCAGG[C/T]GTGGTGGCGCATGCC | 23072 |
rs199676125 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43462126 | CAGCGAGCATCCCCG[-/TC]TGCTTTCCCACCTGG | 23072 |
rs199680865 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237840 | CAGTCTTTCCCCCCC[-/G]CCGCCCCCACTTGGA | 23072 |
rs199682382 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43553625 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 23072 |
rs199687552 | in-del | -/TA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43253130 | CAAACATCCGCACTT[-/TA]AAAAAAAAAAAAAAT | 23072 |
rs199697425 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343116 | GTGCTGATCTATCTC[A/T]GTCTAATTCATCAAC | 23072 |
rs199705460 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247394 | GGCTCATGCCTGTAA[-/T]CCAGCACTTTGGGAG | 23072 |
rs199717525 | snp | C/G | | | missense | HECW1 | GRCh38.p7 | 7:43312032 | GGACCTGGTCATCCA[C/G]TGGGACATAAAGGAG | 23072 |
rs199726524 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43230898 | TTTAAAAAAAATAAA[A/T]TAAAGCAGAAAGGGA | 23072 |
rs199733785 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429317 | ATATATATATATATA[C/T]ATATATATATATATA | 23072 |
rs199752905 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135994 | CTTTTTTTTTTTTTT[A/T]CTATTTGCTGATAGC | 23072 |
rs199754933 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43279813 | CTCCCTGAAACTCTA[C/T]GTTGCTTGAGAACAG | 23072 |
rs199755723 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184020 | TTATTATTATTATTA[-/T]TTTTTTTTTTTGAGA | 23072 |
rs199761622 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250121 | TTTTTTAACCAAAAC[A/G]CACACACACACACGC | 23072 |
rs199787620 | snp | A/G | 1.6604e-05 | 0.00288127 | missense | HECW1 | GRCh38.p7 | 7:43444380 | AGGGCAGTGTCCCCG[A/G]TGGTCCAGGGAACCA | 23072 |
rs199791749 | in-del | -/GTGC | 0.107341 | 0.205301 | intron-variant | HECW1 | GRCh38.p7 | 7:43361049 | TCCTATTTTGTTCTT[-/GTGC]GTGCGTGCGTGTGTG | 23072 |
rs199805512 | snp | A/G | 0.00104359 | 0.022819 | missense | HECW1 | GRCh38.p7 | 7:43444298 | AACCTGATGGAAAGC[A/G]GCAGTGGGGAACCTC | 23072 |
rs199809428 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413451 | TGTGCAGAAGCTCTT[G/T]AGTTTAATTAGATCC | 23072 |
rs199831977 | in-del | -/ATC | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43560215 | TTAACATAGAGAGAA[-/ATC]ACTGTAACCATCCTA | 23072 |
rs199843180 | in-del | -/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114736 | ACAGTTCTCTTTTTT[-/G]TTTGGAGTAGTTTTT | 23072 |
rs199859744 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517863 | GATGAGAAGTCACCA[C/T]AGAATGTACGGGATT | 23072 |
rs199867554 | snp | A/G/T | 0.000845666 | 0.0205471 | intron-variant | HECW1 | GRCh38.p7 | 7:43469121 | GTGAGTGTGACCCAC[A/G/T]TGCGGGGCTTTCATC | 23072 |
rs199872424 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43476468 | AAAGTGATTCTAAAC[-/A]AAATCCCAATAGAAC | 23072 |
rs199899207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43443186 | GATGCCTCATAATTT[G/T]ATTTTTGCTCTTCTT | 23072 |
rs199905645 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43330988 | TTATTTATTTATTTA[-/T]TTTATTTTTTTATAT | 23072 |
rs199911786 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43489845 | TGCCCTACATTACGA[C/T]CTGCAATATCACACA | 23072 |
rs199913481 | snp | A/G | 9.93756e-05 | 0.00704826 | missense | HECW1 | GRCh38.p7 | 7:43469008 | ATTTTGAACGCTACC[A/G]GCACAACCGGGACTT | 23072 |
rs199925925 | in-del | -/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523212 | TTCTCCATGTTGGCC[-/G]GGGGGGGGTCTCGAA | 23072 |
rs199927002 | in-del | -/TC | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43347979 | ATCGGTATGTAGTTT[-/TC]TTTTTTGGTTAAGTC | 23072 |
rs199931013 | in-del | -/T | 0.0275645 | 0.114116 | intron-variant | HECW1 | GRCh38.p7 | 7:43495985 | AATCATTAGAAAAGG[-/T]TTTTTTTTTAAGTAA | 23072 |
rs199936484 | snp | C/T | 0.00014903 | 0.00863092 | utr-variant-5-prime, intron-variant | HECW1 | GRCh38.p7 | 7:43243886 | CCAGGAATTGATGCG[C/T]GTACACGTGGTGGGT | 23072 |
rs199955461 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43261869 | ATTTTTTATTTTTTA[-/T]TTTTTTTTAATTTTT | 23072 |
rs199970050 | snp | A/G | 0.000134785 | 0.00820817 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43550450 | TTCCTACAAGGTCAC[A/G]GAAAGGGAGTTGAAG | 23072 |
rs199976878 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43414162 | GTTCTCCTTGAAGAG[A/G]TCCTTCACATCCCTT | 23072 |
rs199977433 | in-del | -/ATATATAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307890 | ACTATATATATATAT[-/ATATATAC]ACATATATATATATA | 23072 |
rs199979675 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43172441 | TAGGATTTTTTTTTC[G/T]ATAAATTCTTTCACA | 23072 |
rs199990819 | in-del | -/C | 0.040671 | 0.13668 | intron-variant | HECW1 | GRCh38.p7 | 7:43216299 | TACAGGTGTGCACCA[-/C]CATGCCCAGCTAAGT | 23072 |
rs199996837 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43474099 | TATAGTGTGAAGACA[A/G]TAACAGAAAAACCAG | 23072 |
rs200007898 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43209185 | GGCATCAGACCCACT[C/T]GCCCCTCACAATCTT | 23072 |
rs200016783 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125511 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGTCAAGG | 23072 |
rs200027913 | in-del | -/GA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155666 | CTCTCTACTCAGTTT[-/GA]GTATTACCGTTTTGA | 23072 |
rs200042969 | in-del | -/CC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335969 | CTCCTTCCTTCCTTT[-/CC]CTCTCTCTCTCTTTC | 23072 |
rs200043164 | snp | C/T | 1.65839e-05 | 0.00287953 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444285 | CAGCCCCATGAACAA[C/T]CTGATGGAAAGCGGC | 23072 |
rs200043850 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43295108 | GAATAGTCACTTATG[A/C]CTTAGTCTGGCTTAG | 23072 |
rs200044868 | in-del | -/AT | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43480641 | TGTGTGTGTGTGTAC[-/AT]ATGTGTGTGTGTGTG | 23072 |
rs200062919 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237830 | TGCAATTCACCAGTC[-/T]TTCCCCCCCGCCGCC | 23072 |
rs200063019 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355992 | GACTCCGTTAAAAAA[-/AT]AAATAAAATGAAATA | 23072 |
rs200076235 | snp | A/G/T | 0.000149487 | 0.00864423 | missense | HECW1 | GRCh38.p7 | 7:43508029 | TCAGGCTCATTATTC[A/G/T]CCGGGATCATTTGTT | 23072 |
rs200089893 | snp | C/T | 0.00129961 | 0.0254581 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43311813 | CATGGCGTCTCCTTC[C/T]AGAAACTCCCAGAGC | 23072 |
rs200090612 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376966 | TTAGTGAAAAAAAAA[C/T]ACTTTTCTTCAGGTA | 23072 |
rs200112309 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440092 | CCCACCGTGGTTAGG[-/A]GCAGAGTGTTGGGGT | 23072 |
rs200118170 | snp | C/G | 1.65682e-05 | 0.00287817 | missense | HECW1 | GRCh38.p7 | 7:43466544 | CACCAACCCCGAGTT[C/G]TTCACTGTGCTACAT | 23072 |
rs200124950 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43398615 | TATATCTAGGCTGAA[A/G]AAAAAAAAAAAGAAG | 23072 |
rs200127347 | in-del | -/A | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111406 | CTTAGCTAAGGTTTG[-/A]AAAATGGTCTGCTTT | 23072 |
rs200132822 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43491538 | CTCTTTAACAAATTT[A/T]TGATGAGAAATGTTT | 23072 |
rs200135192 | snp | A/G | 0.00215065 | 0.0327215 | missense | HECW1 | GRCh38.p7 | 7:43444619 | GCCCCAGCCAGCACC[A/G]AGGAGGAGCCCTTGG | 23072 |
rs200137726 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110702 | ACTCGGGAGGCTGAG[A/G/T]GGGGAGAGTTGCTTG | 23072 |
rs200148286 | in-del | -/AC | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43499660 | AAAGATTAAAAAAAA[-/AC]ATCCTTAATTTTCCC | 23072 |
rs200150199 | in-del | -/TG | 0.0232847 | 0.105357 | intron-variant | HECW1 | GRCh38.p7 | 7:43539764 | GCCACAACCCTACTA[-/TG]TCATGTTAGAAGCAT | 23072 |
rs200151811 | in-del | -/AA | 0.0138799 | 0.0821421 | intron-variant | HECW1 | GRCh38.p7 | 7:43488122 | AAAACCAGCCTGGCC[-/AA]AACATGGCAAAACCC | 23072 |
rs200159423 | snp | A/T | 1.65811e-05 | 0.00287929 | missense | HECW1 | GRCh38.p7 | 7:43311857 | AGGAGCCGCTCCGAT[A/T]CAGCTACAACCCCGA | 23072 |
rs200175513 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43479472 | GTTTTGAGTAGATTA[A/G]AAAAGGAAGTAGGGG | 23072 |
rs200182230 | in-del | -/ATAAG | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43202444 | GCATACATAATTATT[-/ATAAG]ATTATAATCATAAAA | 23072 |
rs200195238 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307893 | ATATATATATATATA[C/T]ATACACATATATATA | 23072 |
rs200204580 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43525747 | TTGTGAACGATAAAT[G/T]GGAATCACTATAGAC | 23072 |
rs200208944 | snp | C/G/T | 8.40716e-05 | 0.00648306 | missense, synonymous-codon | HECW1 | GRCh38.p7 | 7:43554599 | TCGTGCAGGTTACCA[C/G/T]GATGGGCATCTTGTG | 23072 |
rs200210217 | in-del | -/CCT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546088 | TCTAGATCTTCTTCC[-/CCT]TCTGAACCTGGCACT | 23072 |
rs200211526 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43276456 | ACATTTTAAAAAATA[-/T]ATAGGTAATAAGATA | 23072 |
rs200211596 | in-del | -/TTC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336101 | TTTCTCTTTCTTTCT[-/TTC]TTCTTTCTTTCTTTC | 23072 |
rs200212028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118511 | ATGAAATCAATCAGC[A/G]AGTGATTCCTCATCC | 23072 |
rs200213322 | in-del | -/AGGAAGGAAGGAAGGA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488325 | AAAAAAGAAAGAAAG[-/AGGAAGGAAGGAAGGA]AGGAAGGAAGGAAGG | 23072 |
rs200226327 | snp | C/T | 0.00199792 | 0.0315431 | missense | HECW1 | GRCh38.p7 | 7:43320728 | AGATCGATGCCAGCT[C/T]GTACTTTGTGGAACG | 23072 |
rs200228905 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429301 | ATGCATATATATATA[C/T]ATATATATATATATA | 23072 |
rs200230316 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43378970 | CCAGACATAGAACAT[-/G]GGGTGGTTATTGCTT | 23072 |
rs200234231 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43469057 | GTTCGCAGACACTCG[A/G]CTGGAACTGCCCCGG | 23072 |
rs200234447 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43313379 | TTTTGCTCTTGTTGC[A/C]CAGGCTGGAGTTCAG | 23072 |
rs200234692 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43346257 | ATTAGTGATGTTGAG[C/T]ATTTTTTCATATGTT | 23072 |
rs200236689 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43229634 | ACCTAAAATAAAAGT[A/T]AAAAAAAAAATTAAT | 23072 |
rs200238048 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247941 | GGAAAAAAGAGAGAG[-/A]AAAAAAGGAGGGAAG | 23072 |
rs200239862 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335797 | TTCTTCCTTCCTTCC[A/T]TCCATCTCTTTCCTT | 23072 |
rs200259500 | snp | A/C/G | 3.35852e-05 | 0.00409774 | intron-variant | HECW1 | GRCh38.p7 | 7:43466606 | GGGGCGGCCTGGCTC[A/C/G]GCAAGACCCAAAACA | 23072 |
rs200264664 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43303937 | GAGAGGGAGAGGAGG[-/A]CCCAGGGGCAGTATT | 23072 |
rs200279363 | snp | A/C | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247241 | CAATGGAAGAAATAT[A/C]CAGGAAAACTTGGTT | 23072 |
rs200283168 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43346874 | TTTTATACCAGTACC[-/A]TGCTGTTTTGGTGAC | 23072 |
rs200301111 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43273856 | GTTGTAAAATATGAT[-/TC]TTTTTTTTTTTTTTG | 23072 |
rs200319372 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429319 | ATATATATATATATA[C/T]ATATATATATATATA | 23072 |
rs200321721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43423875 | ATCCTGTAAGACTGA[C/T]ACCAAAAATCAAAGG | 23072 |
rs200324723 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43552320 | TGACTGGCGGAATAA[C/T]ACTGAGTACCGGGGA | 23072 |
rs200334739 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335820 | CTTTCCTTTTCTTCA[C/T]TTTTCCTCTTTCTCC | 23072 |
rs200335429 | in-del | -/GTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43533622 | GAAGATGCCATAGTG[-/GTT]GTTAGAAGAGGCCTT | 23072 |
rs200336015 | in-del | -/GTGATGTGGTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43452985 | GGGAGAAGGCAGCAG[-/GTGATGTGGTT]AGCGAACTAGCAAGG | 23072 |
rs200336346 | in-del | -/GT | | | intron-variant, splice-donor-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161716 | GGGTGAACTTCCAAG[-/GT]CTCTGTATCACTAAG | 23072 |
rs200362403 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198450 | TCACACACTCACCCA[C/T]CCTAACACGTACCCA | 23072 |
rs200368928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43387549 | GACATGCAGAAAATG[C/G]TAACAGCAGCAAGAC | 23072 |
rs200425502 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454838 | AAGCTATGGCTTTTC[-/T]CACTGAAAAGGCTGG | 23072 |
rs200427298 | snp | C/T | 0.000394883 | 0.0140458 | missense | HECW1 | GRCh38.p7 | 7:43444992 | AGGTGGACACGGTGG[C/T]CGCTGACCCGTCTGC | 23072 |
rs200438526 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43502494 | GACCTCATCTCTACC[-/A]AAAAAAAATTTTTTT | 23072 |
rs200441448 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43253130 | CAAACATCCGCACTT[A/T]AAAAAAAAAAAAAAA | 23072 |
rs200441795 | in-del | -/TTATTTATTTAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43304460 | ATTCATTCAACACAG[-/TTATTTATTTAT]TTATTTATTTATTTA | 23072 |
rs200442825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43324261 | ACTAATGTAGTATAA[C/T]TTGTCAAAAAGTAAA | 23072 |
rs200443966 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43407346 | ATTTTACACCCGGAC[A/C]CATCAAATTTCCAAA | 23072 |
rs200446981 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43191959 | GACCTAGTTGTTGTT[G/T]TTTTCTTTTTTTTTT | 23072 |
rs200451115 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242809 | GGAAGCCAGTGGCTG[G/T]GGCAGGGAGCGGGAA | 23072 |
rs200457567 | in-del | -/AG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43165682 | CCACTCTAATCACTT[-/AG]ATTTTTTTTTAGTAA | 23072 |
rs200458933 | snp | C/T | 0.00041468 | 0.0143933 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43407656 | ACACAGCATCTTCCC[C/T]GCCCTCCCTCACCAT | 23072 |
rs200470244 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131099 | GGTGAAACCCCATCT[C/G]TACTAAAAATACAAA | 23072 |
rs200470669 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43501179 | AACTGACTTTCTTTT[C/T]TTTCTTTTTTTTTTT | 23072 |
rs200475668 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43551970 | GCTCTCATATCTAAG[-/C]ACCCCCCCAAAGGCC | 23072 |
rs200484093 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43393676 | ACTCTTTTTTCTTCT[-/TC]TTTTTTTTTTTTCAT | 23072 |
rs200493135 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43268015 | TATCACAGACAAATA[A/T]AGAACACTTGCCACT | 23072 |
rs200504185 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43553672 | AGATTCTGTCTCAAA[A/G]AAAAAAAAAAAAAAA | 23072 |
rs200535467 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43340515 | TGTGAGCCACTGCGC[A/C]CGGCCTCTAATTACC | 23072 |
rs200539575 | snp | G/T | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297546 | GCCATTCTCCAAGGT[G/T]GTTGGCAGGGATGTC | 23072 |
rs200543552 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43383832 | GCCTTGCCAGTAACA[A/G]TTGATTAACATATTT | 23072 |
rs200544206 | snp | C/T | 1.85775e-05 | 0.00304769 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445503 | GCTGGCCGCCCCTAG[C/T]GGGCACGTGGAAAGA | 23072 |
rs200549707 | in-del | -/ATTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412460 | TTTATTTATTTATTT[-/ATTT]TAATTATTATACTTT | 23072 |
rs200566652 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422927 | AATCGCAGTGCCTGG[C/T]CGAGAGTCGTGGTCT | 23072 |
rs200576607 | in-del | -/TGTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467118 | TCAACAAACATTTTC[-/TGTT]TGTGGTTCAGGCTCA | 23072 |
rs200577808 | snp | C/T | 0.481242 | 0.0950111 | intron-variant | HECW1 | GRCh38.p7 | 7:43373222 | TTTTTTTTTTTTTTT[C/T]TTTTTGAGACAGAGT | 23072 |
rs200579671 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43344210 | CCATTCTGTAGGTTG[C/T]CTGTTCACTCTGATG | 23072 |
rs200590983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43315140 | ATAAGAGGGGGAAGA[C/T]ACCTGGATGTAGAGG | 23072 |
rs200604736 | in-del | -/TAGA | 0.030278 | 0.119257 | intron-variant | HECW1 | GRCh38.p7 | 7:43425288 | ATGTGGATAGCTAGG[-/TAGA]TAGATAGATAGATGA | 23072 |
rs200626288 | in-del | -/AGAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488421 | AAGAAAGAGAGAGAG[-/AGAA]AGAAAGAAAGAGAAA | 23072 |
rs200626702 | in-del | -/T | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43377641 | TGCACAGAAATAACA[-/T]TTTTTTTCTCTTTGT | 23072 |
rs200632696 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247762 | GAGGGAGGAAGGGAA[-/AG]AGAGGAAAAAAGAGA | 23072 |
rs200636506 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43187056 | CATGAGGTTGCAGTC[-/AAG]ACGTCAGTCAAAACT | 23072 |
rs200646467 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413892 | GTCAGGTAGTGTGAT[G/T]CCTCCAGCTTTGTTC | 23072 |
rs200647088 | snp | A/G/T | 5.0257e-05 | 0.00501262 | intron-variant | HECW1 | GRCh38.p7 | 7:43466413 | AATGCCTTTTTCCCA[A/G/T]TGCATTCTGTTGCTT | 23072 |
rs200680129 | in-del | -/T | | | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563006 | TATTTTTTTTTCACA[-/T]TTTTTTTTTCCTTTT | 23072 |
rs200690095 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237080 | GAGAAGGAGGGAGGG[-/A]GGGAGGAAGCAGGGA | 23072 |
rs200693960 | in-del | -/AG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43165031 | ACTGCTCCCTTGTTT[-/AG]CAGAACATTTCCACT | 23072 |
rs200694032 | in-del | -/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248063 | AGAGGAAGGAAGGAA[-/G]GGAGGGAGGGAGGGA | 23072 |
rs200698253 | in-del | -/TG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43317810 | CTTTTTTCTCATTAT[-/TG]TGTGTGTGTGTGTGT | 23072 |
rs200707993 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43388164 | CACACCATATTGTAC[A/C]CCTGCCTGTGACCAC | 23072 |
rs200717791 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336172 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 23072 |
rs200719976 | in-del | -/GTCAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187061 | GGTTGCAGTCAAGAC[-/GTCAG]TCAAAACTACAATGT | 23072 |
rs200721302 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43306842 | GTGATGATTTTCTGC[-/T]TTTAAGATTCTGTTT | 23072 |
rs200722132 | in-del | -/AAGG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247731 | AAGAAGGAAGGAAGA[-/AAGG]AAGGAAGGAAGGAGG | 23072 |
rs200739128 | in-del | -/ATATATATATATATAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429290 | CCATATATTATATGC[-/ATATATATATATATAT]ATATATATATATATA | 23072 |
rs200743129 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43324049 | AAAAAAGAAAAAAAA[-/C]AGGCTTGCAGAAGGC | 23072 |
rs200748119 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43246141 | ATTTCTATGAAAAAT[-/A]AAAAAAAAAAAATTA | 23072 |
rs200778134 | in-del | -/G | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247833 | GAGAGAGAAAGGTAA[-/G]GAAGGAAGGAAGAAG | 23072 |
rs200787859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118107 | GTGCCCATGATGACA[A/G]ATGCCATCATGGAGA | 23072 |
rs200790109 | in-del | -/AA | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43164385 | AACAGTGTTTTGCAT[-/AA]GTTGAGTTGAAGGTG | 23072 |
rs200801363 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43431880 | TCCCACCGACACTTG[C/T]TTTTTTTTTTTTTTG | 23072 |
rs200817273 | snp | A/G | 0.00110919 | 0.0235237 | missense | HECW1 | GRCh38.p7 | 7:43463751 | CCAGCAGGAGGAGGC[A/G]GAGGTGGAGGGAGTG | 23072 |
rs200822928 | snp | C/T | 0.000414219 | 0.0143853 | synonymous-codon, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509095 | GATCAGCCCCATGTC[C/T]GCATTTGTAGAAAAC | 23072 |
rs200837983 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343117 | TGCTGATCTATCTCT[A/G/T]TCTAATTCATCAACT | 23072 |
rs200841871 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413041 | CACACTGACTTCCAC[A/G]ATGGTTGAACCAGTT | 23072 |
rs200845522 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43357078 | CAGGACAGGGAGCAA[A/C]AAATGCTGGTGAGAA | 23072 |
rs200850790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43233556 | CCTCTCCTTCCCCCA[A/G]ATAATAACTTCCATA | 23072 |
rs200859187 | in-del | -/TATG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480642 | GTGTGTGTGTGTACA[-/TATG]TGTGTGTGTGTGTAT | 23072 |
rs200861371 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43390549 | TCTTAAAAAAAAAAA[-/C]AAAAAAAAAACAGCA | 23072 |
rs200861749 | in-del | -/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43477712 | ATTTACCTTTTTCCT[-/G]GGGGGGTGTATTTTT | 23072 |
rs200875716 | in-del | -/AGGCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226696 | GCCTGTGAGGGGAAA[-/AGGCC]AGGCCTGACCCTCCT | 23072 |
rs200882150 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43227828 | AAAGCAATACATCCA[C/T]GAAACTGCACAACTC | 23072 |
rs200885508 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43177626 | CACCTGTGTGAGTCT[A/G]GGCAAGTGACTTAAT | 23072 |
rs200886554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43172449 | TTTTTTCAATAAATT[C/G]TTTCACACATGCCCA | 23072 |
rs200886623 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43431881 | CCCACCGACACTTGC[-/T]TTTTTTTTTTTTTGA | 23072 |
rs200897031 | in-del | -/AT | 0.16028 | 0.233346 | intron-variant | HECW1 | GRCh38.p7 | 7:43307928 | TATATACACACACAC[-/AT]ATAGTGAAATGTATT | 23072 |
rs200903300 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | HECW1 | GRCh38.p7 | 7:43480736 | ATATATATATATATA[C/T]ACACACACACACATA | 23072 |
rs200912368 | snp | A/G | 0.00287955 | 0.0378349 | missense | HECW1 | GRCh38.p7 | 7:43508059 | TGGAGGGAACCTTCA[A/G]TCAGGTGATGGCCTA | 23072 |
rs200914444 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43170366 | ATCCTCCCCCACCCC[-/T]GTCTGTGGAAAAATT | 23072 |
rs200916311 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224910 | GAGGGAGTGGCTGGG[C/T]GAGGCCTGGAAAAAG | 23072 |
rs200929407 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43351679 | TTTTTTTCTTTCTTC[-/T]TTTTTTTTTTTTTTT | 23072 |
rs200929568 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480624 | GTTTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTA | 23072 |
rs200945823 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43417285 | AAACTCCTGACCTCA[A/G]GTGATCCACCCGCCT | 23072 |
rs200967853 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307895 | ATATATATATATATA[C/T]ACACATATATATATA | 23072 |
rs200969113 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247832 | AAGAGAGAGAAAGGT[-/AAG]AAGGAAGGAAGAAGG | 23072 |
rs200972152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43397399 | TTTCATGAATGTACC[A/G]TGGTTCCATCTGTCA | 23072 |
rs200973212 | snp | A/G | 3.31411e-05 | 0.00407056 | missense, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509096 | ATCAGCCCCATGTCC[A/G]CATTTGTAGAAAACC | 23072 |
rs200978295 | in-del | -/GAAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488404 | AGGAAGGAAGGAAAT[-/GAAA]GAAAGAGAGAGAGAG | 23072 |
rs200980332 | snp | G/T | | | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295694 | CCTACGTATTTTCCA[G/T]CTCCTTTAAAGACCT | 23072 |
rs200981481 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429324 | TATATATATATATAT[A/G]TATATATATATACAT | 23072 |
rs201001666 | in-del | -/AAAG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247812 | GGAGGGAAGGAAAGA[-/AAAG]AAAGAGAGAGAAAGG | 23072 |
rs201002842 | snp | C/G | 0.00011969 | 0.00773502 | intron-variant | HECW1 | GRCh38.p7 | 7:43320790 | GACATGGATGAAGCA[C/G]AATTCAACTGTTTCA | 23072 |
rs201003324 | in-del | -/AGAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189606 | CATTAAAAAAAAGAA[-/AGAG]AGAAAACTTGACCTT | 23072 |
rs201003568 | in-del | -/AAAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189600 | AAAACACATTAAAAA[-/AAAG]AAAGAGAGAAAACTT | 23072 |
rs201017639 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544596 | CTTTGACTCAGCACA[C/T]GTCTAGAAATTTGTC | 23072 |
rs201030724 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43436014 | CTAAAAATACAAAAA[-/A]TTAGCTGGACGTGGT | 23072 |
rs201037333 | snp | C/T | 0.000530627 | 0.0162798 | intron-variant | HECW1 | GRCh38.p7 | 7:43479753 | TGGAGAGGTAACCCT[C/T]CCTACACCCCGCCCT | 23072 |
rs201038187 | in-del | -/AAAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43230891 | GCCAAGATTTAAAAA[-/AAAT]AAATTAAAGCAGAAA | 23072 |
rs201045255 | in-del | -/GAGAGA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487978 | GAAGAGAGAGAGAGA[-/GAGAGA]AAGAAAAAAGAAAGA | 23072 |
rs201046334 | snp | A/G | 0.00199806 | 0.0315443 | intron-variant | HECW1 | GRCh38.p7 | 7:43466623 | CAAGACCCAAAACAC[A/G]GCTTTGTAAAGTCAT | 23072 |
rs201075510 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43457808 | AAAAAACATGGAAAC[-/A]AAAAAATAAAAATGA | 23072 |
rs201081033 | in-del | -/TGCCTCCCACC | 0.0298908 | 0.118541 | intron-variant | HECW1 | GRCh38.p7 | 7:43459079 | CCCATGGCAGGAAAA[-/TGCCTCCCACC]TGCCTCCCACCTGCC | 23072 |
rs201086058 | snp | A/T | 6.72868e-05 | 0.0057999 | missense, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43311781 | CTGTACCAGAACAGG[A/T]TTTTAGGCCTGGCCG | 23072 |
rs201089900 | snp | C/T | 1.6566e-05 | 0.00287797 | missense | HECW1 | GRCh38.p7 | 7:43311935 | CCATTCCCCGCTCCA[C/T]CAGCGACACTGACCT | 23072 |
rs201094367 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43273337 | GTTGAAAAAAATAAA[G/T]ATAAATAAATAAATA | 23072 |
rs201133014 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556697 | ATTAAAAAAAAAAAA[-/A]GAAAGAAAAAAGAAA | 23072 |
rs201158360 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147647 | TCAGGTCATGTACCC[-/T]TTTTTTTAATTAAAA | 23072 |
rs201158657 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43199150 | GCTCCCGCTCAGGGA[G/T]CAGCCTCTGTGCTTC | 23072 |
rs201174011 | snp | A/G | 0.000136414 | 0.00825763 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43407584 | AGCCATGGGGTTGAA[A/G]AAAGGGATGTTTTTC | 23072 |
rs201180355 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43450174 | CTCTTTCCGGAGCAC[C/G]CTGGCTTGTCTGATT | 23072 |
rs201182663 | snp | A/G | 8.34801e-05 | 0.00646012 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43311804 | CCTGGCCGCCATGGC[A/G]TCTCCTTCTAGAAAC | 23072 |
rs201184322 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43223632 | TCAAAAAAAAAAAAA[-/A]TATGCCAAGTTGTGT | 23072 |
rs201188734 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43415163 | ATTTTGCAGCGGCTG[A/G]TACCGGTTGTTCCTT | 23072 |
rs201191917 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43337813 | ATGGAGCACAATGTC[-/T]TTTTTTTTTATAGAA | 23072 |
rs201195862 | snp | C/T | 0.499 | 0.0223418 | intron-variant | HECW1 | GRCh38.p7 | 7:43345807 | ATATATATACACACA[C/T]ACACACACACACACA | 23072 |
rs201202223 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335980 | CTTTCCCTCTCTCTC[-/T]CTTTCTCTCTCTCTC | 23072 |
rs201204524 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43503236 | AGCTTTGCTGGAGCC[A/G]ACATCAATACAGTCA | 23072 |
rs201206998 | in-del | -/TTCAGA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43407969 | AGTAGCCTCTTCTGA[-/TTCAGA]ACCCATGCCGCGAGC | 23072 |
rs201207953 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132154 | TTGCATCTCCACACA[C/G]CCCCTCACAGCGCCC | 23072 |
rs201217958 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348103 | GTACCAATTCATCTT[A/T]CAATGTCTGGTAGAA | 23072 |
rs201225073 | snp | C/T | 5.02483e-05 | 0.00501215 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445335 | CACGCGCTTCTCCTC[C/T]GTGGACAGCGCCAAG | 23072 |
rs201226108 | in-del | -/GCCATC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43542126 | ATATCCACATTGTTG[-/GCCATC]CAATCTCCAGAACTT | 23072 |
rs201232229 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43486461 | CACGCACCCCTACAC[C/G]CGGCTAATTTTTTGT | 23072 |
rs201233516 | in-del | -/ATATATATACACAC | 0.0551013 | 0.156571 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376030 | ATATATGAAATATGT[-/ATATATATACACAC]ATATATATACACACA | 23072 |
rs201243211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43363969 | CTGGGGACTTGAGCA[C/T]ACAGTTTCTAAGGGG | 23072 |
rs201250310 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336140 | TCTCTCTCTCTCTCT[C/T]TCTTTCTCTCTCTCT | 23072 |
rs201253738 | snp | G/T | 0.459233 | 0.136827 | intron-variant | HECW1 | GRCh38.p7 | 7:43415262 | TTGCTTGTCTGTAAA[G/T]TATTTTATTTCTCCT | 23072 |
rs201254518 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184022 | ATTATTATTATTATT[-/A]TTTTTTTTTGAGACA | 23072 |
rs201264544 | in-del | -/C | 0.0126979 | 0.078662 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132166 | CAGCCCCTCACAGCG[-/C]CCCCCCCGCCCCAAG | 23072 |
rs201266010 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43540895 | CTTGGGTCCTCATTC[A/T]CCACGGTCTGAAAAA | 23072 |
rs201278562 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119180 | CTTTTGCCTGTCTTG[A/G]GAGCACCTCGATCAG | 23072 |
rs201294883 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43191136 | ATTAACACTCTTGGG[-/TT]TTATATATATATATG | 23072 |
rs201297726 | snp | A/G | 0.00199792 | 0.0315431 | missense | HECW1 | GRCh38.p7 | 7:43407708 | ATCATAGGCAACACC[A/G]TGAACCCCATCTGGC | 23072 |
rs201303645 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43404319 | GAAGAAACATGTGCT[-/C]TTGAGTAGAAGTCTC | 23072 |
rs201311774 | in-del | -/T | 0.251859 | 0.249993 | intron-variant | HECW1 | GRCh38.p7 | 7:43440095 | CCGTGGTTAGGAGCA[-/T]GAGTGTTGGGGTGAT | 23072 |
rs201315890 | in-del | -/TTTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43401574 | TAAAAAGGTTTTTTT[-/TTTG]TTTTTTTTTTTTCCC | 23072 |
rs201318187 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343915 | ACATCCTCTCCAGCA[C/T]CTGTTGTTTCCTGAC | 23072 |
rs201324045 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250137 | CACACACACACACGC[A/G]CACACACACATACAC | 23072 |
rs201336453 | in-del | -/CTTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336077 | TCTTTCTTCCCCTCC[-/CTTT]CTTTCTTTCTCTTTC | 23072 |
rs201342808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189866 | CCAGTTCCAAAAGTG[C/T]CTGGTATATAGAATA | 23072 |
rs201343318 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43425304 | AGATAGATAGATAGA[A/T]GATAGATAGATAGAT | 23072 |
rs201364765 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43313414 | GCGATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC | 23072 |
rs201366402 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43230894 | AAGATTTAAAAAAAA[A/T]AAATTAAAGCAGAAA | 23072 |
rs201369649 | in-del | -/T/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43455136 | GTTTTCTTTTTTTTT[-/T/TT]GTTTTCTTTTGTTTT | 23072 |
rs201389596 | snp | C/T | 0.000648186 | 0.0179909 | missense | HECW1 | GRCh38.p7 | 7:43445052 | GGGCTACTCCAGGCA[C/T]GGCGCACCCTGGCCA | 23072 |
rs201405323 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43449796 | GAACCATCTGAAAAA[A/G]GGGCCATCCTTTGTC | 23072 |
rs201409706 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43537796 | CACAGTTATTTTTTT[A/T]AAAAAAGCTATGGCT | 23072 |
rs201416210 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43340839 | ATTATAAATCATGCT[A/G]CTATAAAGACACATG | 23072 |
rs201416510 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343115 | TGTGCTGATCTATCT[A/C]TGTCTAATTCATCAA | 23072 |
rs201420866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43450659 | TTTTTAAAAAAATAT[C/T]TCCCCCCTCACGAAT | 23072 |
rs201420939 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335981 | TTTCCCTCTCTCTCT[C/T]TTTCTCTCTCTCTCC | 23072 |
rs201436117 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343030 | ACTCCATCTCAAAAG[-/A]AAAAAAAAAATGTTT | 23072 |
rs201438024 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358818 | TCCTTAAAATATATT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs201440610 | in-del | -/CAAGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43456632 | TTTGGAGGCGAGAGA[-/CAAGT]TAAGCTTGAGTGTCA | 23072 |
rs201444322 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488327 | AAAAGAAAGAAAGAG[A/G]AAGGAAGGAAGGAAG | 23072 |
rs201447283 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376038 | ATATGTATATATATA[-/TA]CACACATATATATAC | 23072 |
rs201449657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43544597 | TTTGACTCAGCACAC[C/T]TCTAGAAATTTGTCC | 23072 |
rs201464180 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307070 | TCTGCTACAAATAGG[-/A]AAAAAAAACCAAAAA | 23072 |
rs201483667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120437 | TGTGCTATTCTCTGT[C/T]TCCCCTTCTAACTTG | 23072 |
rs201492332 | in-del | -/GAAA | 0.468084 | 0.122226 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247856 | GAAGAAGGAAGGAAG[-/GAAA]GAAAGAAAGAAGAAA | 23072 |
rs201500062 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413395 | AAAATTTTCTCCCAT[G/T]TTGTAGGTTGCCTGT | 23072 |
rs201510541 | snp | A/G | 0.000331148 | 0.0128633 | utr-variant-5-prime, intron-variant | HECW1 | GRCh38.p7 | 7:43243887 | CAGGAATTGATGCGC[A/G]TACACGTGGTGGGTC | 23072 |
rs201511376 | snp | C/G/T | 0.00149717 | 0.0273196 | missense | HECW1 | GRCh38.p7 | 7:43492112 | GAGGAGCCTCTTTAC[C/G/T]GGCCAGGCCAGGACA | 23072 |
rs201515538 | snp | A/C/T | 3.86556e-05 | 0.00439617 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445101 | CAGCCTGGCCAATGG[A/C/T]GCGGCCCAGGATGGC | 23072 |
rs201521619 | snp | A/G | 4.96997e-05 | 0.00498472 | missense | HECW1 | GRCh38.p7 | 7:43500719 | AAATCCATTACATTC[A/G]GACTGAGGGTAATCA | 23072 |
rs201522591 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43417235 | TTTGTGTTTTTAGTA[C/G]AGATGGGTTTCACCA | 23072 |
rs201525922 | snp | G/T | 0.00199792 | 0.0315431 | intron-variant | HECW1 | GRCh38.p7 | 7:43479582 | TTCTCACACCACACG[G/T]TGCTTTTTTTCACTG | 23072 |
rs201525971 | in-del | -/TG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347278 | TTTAATTTTTTTTTT[-/TG]CAGCTATTGTAAAAG | 23072 |
rs201527192 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43394033 | GTGGACATTTTTAAA[-/T]TAGAATTAGGAGCCA | 23072 |
rs201530520 | in-del | -/CAACTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43459434 | CTTATTTTAAATAAT[-/CAACTG]AAGTTTTATTTTTTA | 23072 |
rs201545934 | snp | C/T | 0.000465596 | 0.0152506 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43320648 | AGATGAGGTCTTGTC[C/T]GAAAACTTTCTGGAC | 23072 |
rs201550489 | in-del | -/CT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198741 | CTCTCACACCCCACA[-/CT]CTCACACACTATAGA | 23072 |
rs201573047 | in-del | -/TTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190083 | TCACAGCTGTGGAAA[-/TTG]TTTTTGTTGTTGTTG | 23072 |
rs201575281 | snp | C/G | 0.000386675 | 0.0138992 | missense | HECW1 | GRCh38.p7 | 7:43445389 | CTCGCAAGACGACGA[C/G]GAGGAGGAGAACAGC | 23072 |
rs201587357 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289106 | AACACTTTCTCTTTT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs201626599 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296507 | CAACTCTGAACTTGG[C/T]GGCGCAGCTGTGGAC | 23072 |
rs201630596 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316789 | CCTCCCCTCCCCTCC[C/T]CTCCTCTCCTCTCCC | 23072 |
rs201671885 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43439170 | CATAAAGAACCTAGC[A/C]CGGCCACTGGCACGT | 23072 |
rs201675550 | in-del | -/AG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43186688 | AAAAAAAAAAAAAAA[-/AG]GATTATCATACCATA | 23072 |
rs201676278 | in-del | -/TTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467124 | AACATTTTCTGTGGT[-/TTG]TCAGGCTCAGATCTA | 23072 |
rs201681339 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440886 | AACAATTTTTAAGTC[A/G]GGGCTTGTTGGGATA | 23072 |
rs201702542 | in-del | -/A | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520658 | TTTAAGGTTTTTTTT[-/A]AAAAAAAACACAAAG | 23072 |
rs201703169 | in-del | -/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520651 | TATTCTACTTTAAGG[-/T]TTTTTTTAAAAAAAA | 23072 |
rs201713558 | in-del | -/TTTA | 0.380333 | 0.213338 | intron-variant | HECW1 | GRCh38.p7 | 7:43412426 | ATGCTTTTCATTTCT[-/TTTA]TTTATTTATTTATTT | 23072 |
rs201714101 | in-del | -/ATAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307894 | TATATATATATATAT[-/ATAC]ACATATATATATATA | 23072 |
rs201732675 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43446409 | AGTGGTATGACTGGG[-/A]AAAAAAAATTGAAAA | 23072 |
rs201738695 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43258926 | GTGCACCCCAGTTTG[-/T]TTTTTTTTGTTTTGT | 23072 |
rs201742349 | snp | A/G | 1.68829e-05 | 0.00290537 | intron-variant | HECW1 | GRCh38.p7 | 7:43507102 | GAAGAAGAAGAAGAA[A/G]GAAAGTGATGACCTC | 23072 |
rs201742683 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336971 | TAGGTTGGTTCCATG[-/A]CTTTGCTATTGTGAA | 23072 |
rs201757499 | snp | C/T | 0.00471076 | 0.0483031 | missense | HECW1 | GRCh38.p7 | 7:43456393 | CGGCAGCAGCCACCC[C/T]GGATGGCATGCGGAG | 23072 |
rs201767426 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118602 | CCTCAAAAGGACTTC[-/T]TTTTTTTCTTTACCG | 23072 |
rs201770658 | in-del | -/A/AA | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43550113 | TCTACCAAAAAAAAA[-/A/AA]GAAGAAGAAGAAGAA | 23072 |
rs201771274 | snp | A/G | 0.000364564 | 0.0134963 | missense | HECW1 | GRCh38.p7 | 7:43396844 | GGTGCTGATGAGACC[A/G]TCCAAGGACAAGGAA | 23072 |
rs201793595 | snp | C/T | 0.0029955 | 0.0385847 | intron-variant | HECW1 | GRCh38.p7 | 7:43311721 | CGGTGACTGAGTTGC[C/T]GGCGTGCCCTGACCC | 23072 |
rs201811956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43528772 | ACATTCATTTCAGTT[A/G]CTAATTAGCAATCCG | 23072 |
rs201838975 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440884 | GAACAATTTTTAAGT[-/C]CGGGGCTTGTTGGGA | 23072 |
rs201853678 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | HECW1 | GRCh38.p7 | 7:43270681 | AAACCAAGGTATTAG[-/A]AAAAATCAATATAGC | 23072 |
rs201857735 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114734 | TGACAGTTCTCTTTT[-/A]TTTTTGGAGTAGTTT | 23072 |
rs201864069 | in-del | -/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130867 | AATGCTCAACCTGTA[-/TT]TTAATAACTGGGTAT | 23072 |
rs201865352 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43395558 | GTCAAAGAATTTGAC[-/A]AATCTCTTATCTGGC | 23072 |
rs201874151 | in-del | -/G | | | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117527 | CCATTGCTTTTCCAA[-/G]GTTAAGACACAATGA | 23072 |
rs201889091 | in-del | -/G | 0.0592355 | 0.161582 | intron-variant | HECW1 | GRCh38.p7 | 7:43165683 | CACTCTAATCACTTA[-/G]ATTTTTTTTTAGTAA | 23072 |
rs201896021 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115316 | TTTTTTTTTTTTTTT[G/T]TCCACTATAGCAAAA | 23072 |
rs201913929 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416841 | AAAGGGAACTCCCTG[A/G]CCCCTTGCGCTTCCC | 23072 |
rs201917173 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43170919 | GGAGGAAAAGAAAAA[C/T]GTTTGTGCAAAAGGT | 23072 |
rs201923562 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422373 | GGTTGTTGTTGTTTT[G/T]TTTTTTTTTTGAGGA | 23072 |
rs201937285 | in-del | -/AGAG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247818 | AAGGAAAGAAAAGAA[-/AGAG]AGAGAAAGGTAAGAA | 23072 |
rs201941496 | in-del | -/AAAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43268009 | ATAGTTATCACAGAC[-/AAAT]AAATATAGAACACTT | 23072 |
rs201948221 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159113 | CTGACAGTTTATTTA[-/T]TTTATTTATTTATTT | 23072 |
rs201959497 | snp | A/G/T | 1.6582e-05 | 0.00287936 | missense | HECW1 | GRCh38.p7 | 7:43501287 | ATAGCTTCTCTCCCC[A/G/T]ATGTTCACCCTGTTC | 23072 |
rs201962425 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43219666 | GAACAGAACAGAACA[-/G]GACAGGGATTTTCAC | 23072 |
rs201969129 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189603 | ACACATTAAAAAAAA[-/G]AAAGAGAGAAAACTT | 23072 |
rs201973618 | in-del | -/TG | 0.317933 | 0.240593 | intron-variant | HECW1 | GRCh38.p7 | 7:43190084 | CACAGCTGTGGAAAT[-/TG]TTTTGTTGTTGTTGT | 23072 |
rs201974973 | snp | C/T | 0.000167427 | 0.00914798 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444597 | ACTGCTGCTGGAAGA[C/T]GGTGAAGCCCCAGCC | 23072 |
rs201980456 | in-del | -/G/GAGAG/GAGAGA/GG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487983 | AGAGAGAGAGAGAGA[-/G/GAGAG/GAGAGA/GG]AAGAAAAAAGAAAGA | 23072 |
rs201984876 | snp | C/T | 7.07176e-05 | 0.00594591 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444888 | GCACAGCATGCCCTC[C/T]GCCCAGGGCGGCAGC | 23072 |
rs201987346 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43486605 | CGTGCCTGGCCTAAT[G/T]TTATTTTTTTAAAGC | 23072 |
rs201987920 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43551978 | ATCTAAGCACCCCCC[A/C]AAAGGCCCCACCTCC | 23072 |
rs202003443 | in-del | -/CACA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480711 | ACACACACACACACA[-/CACA]TATATACGCATATAT | 23072 |
rs202007423 | snp | C/T | 0.0012987 | 0.0254492 | missense | HECW1 | GRCh38.p7 | 7:43554685 | TACTGCAGTTTGTCA[C/T]GGGAACATCCAGCGT | 23072 |
rs202007736 | in-del | -/A | 0.192088 | 0.2432 | intron-variant | HECW1 | GRCh38.p7 | 7:43378810 | ACTGTCTCAAAAAAC[-/A]AAAAATAAAAACAAA | 23072 |
rs202013784 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43273338 | TTGAAAAAAATAAAG[A/G]TAAATAAATAAATAG | 23072 |
rs202019558 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43340973 | ACCATGGAATACTAT[A/G]CAGCCATAAAAAAGG | 23072 |
rs202029095 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43384351 | GATCCAGCAACCCAT[G/T]GGTAGCAGGAAGCCC | 23072 |
rs202032014 | in-del | -/CT/TCCT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335993 | CTCTTTCTCTCTCTC[-/CT/TCCT]TCCTTCCTTCCTTTC | 23072 |
rs202044930 | in-del | -/CCTCC | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248689 | CCTCCTCCTCCTCCT[-/CCTCC]TTTTCCTCCTCCTCC | 23072 |
rs202046488 | in-del | -/AAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347270 | AATTTAATTTAATTT[-/AAT]TTTTTTTTGCAGCTA | 23072 |
rs202048147 | snp | C/T | 9.54699e-05 | 0.00690839 | missense | HECW1 | GRCh38.p7 | 7:43554618 | GGGCATCTTGTGATC[C/T]GCTGGTTCTGGGCTG | 23072 |
rs202051007 | in-del | -/ATTT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159136 | TTTATTTATTTATTT[-/ATTT]TAAAGAGGAATTTTT | 23072 |
rs202052637 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43206141 | CAAATTAATGTACAG[A/G]GGAAACACATGAACT | 23072 |
rs202055016 | snp | G/T | 0.000996065 | 0.0222944 | intron-variant | HECW1 | GRCh38.p7 | 7:43479586 | CACACCACACGGTGC[G/T]TTTTTTCACTGGTCT | 23072 |
rs202061205 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301875 | AGTGGAAACTCTGTC[-/A]AAAAAAAAAAAAAAA | 23072 |
rs202061834 | in-del | -/CT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43495566 | GTGCCCACTCTGCCC[-/CT]TACAACCTGGTCCTC | 23072 |
rs202063581 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | HECW1 | GRCh38.p7 | 7:43271839 | TTTTTACAGAATTGG[-/A]AAAAAACTATGTTAA | 23072 |
rs202079846 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43507692 | TATTTTCCCTTCTGG[A/G/T]TTTATTATTTTCATC | 23072 |
rs202105450 | in-del | -/C | 0.107694 | 0.205546 | intron-variant | HECW1 | GRCh38.p7 | 7:43280995 | TGTTTGGGGCTGTTT[-/C]TCCCCCCATGAAAAT | 23072 |
rs202110890 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429325 | ATATATATATATATA[C/T]ATATATATATACATA | 23072 |
rs202120473 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43346844 | CTATTCTGTTCCACT[A/G]GTCTATGTGCCTATT | 23072 |
rs202122909 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43268013 | GTTATCACAGACAAA[A/C]ATAGAACACTTGCCA | 23072 |
rs202123661 | snp | G/T | 0.00199792 | 0.0315431 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43407638 | TTCCATTCAGCCTGG[G/T]AAACACAGCATCTTC | 23072 |
rs202125340 | in-del | -/A | 0.0908922 | 0.192833 | intron-variant | HECW1 | GRCh38.p7 | 7:43501829 | CTATCTAAAAAAAAA[-/A]TAAAAAAGAAAGAAA | 23072 |
rs202128652 | in-del | -/TCCAATCTCC | 0.0505692 | 0.150756 | intron-variant | HECW1 | GRCh38.p7 | 7:43542130 | CCACATTGTTGGCCA[-/TCCAATCTCC]AGAACTTTTTCATCT | 23072 |
rs202160242 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43483552 | CATGCAAACTCTTTT[G/T]TTTTTTTTTTTTTTG | 23072 |
rs202167289 | in-del | -/ATA | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359574 | GGCCATGCTTATTTC[-/ATA]ATGTCAATTTTTTAA | 23072 |
rs202167665 | in-del | -/GG | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513849 | TAATATTCAGGCCAA[-/GG]AGAGAAAGAGGAGTT | 23072 |
rs202172981 | snp | A/G | 0.00277665 | 0.0371566 | missense | HECW1 | GRCh38.p7 | 7:43444899 | CCTCCGCCCAGGGCG[A/G]CAGCGCGGCAGAGGA | 23072 |
rs202185795 | snp | C/T | 0.208169 | 0.246476 | intron-variant | HECW1 | GRCh38.p7 | 7:43345809 | ATATATACACACACA[C/T]ACACACACACACACA | 23072 |
rs202191988 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247872 | GAAAGAAAGAAGAAA[A/G]CAAGCAAGAAAGGGA | 23072 |
rs202192499 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307901 | ATATATATATACACA[C/T]ATATATATATATATA | 23072 |
rs202195718 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140907 | GACAGAGACAGAAGC[-/AG]AGAGAGAGAGACAGA | 23072 |
rs202206713 | in-del | -/ATT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160796 | ACAAAGGCCAATAAA[-/ATT]GTATCAAATTTCACC | 23072 |
rs202218082 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287654 | TGATTTAGGTTTTTT[A/T]AAGGTTTCTCTGGCT | 23072 |
rs202221652 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43199034 | GGTATGACCACAAAT[C/T]CGATATAAGAGAGTC | 23072 |
rs202230638 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43311949 | ACCAGCGACACTGAC[C/T]TGGTCACCTCGGACA | 23072 |
rs202231311 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139813 | TTCATCTTTGGAAAA[A/G]GGGCAAATTTGGGGA | 23072 |
rs207467818 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43186579 | GAGGCTGAGGCAGGA[C/G]AATGGCATGAACCTG | 23072 |
rs207467819 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43337063 | GGTAGGTACCTAGTA[A/G]TGGGTTTGCTGGATC | 23072 |
rs207467820 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511843 | GGAAGCTAGGAGAGC[C/T]CAGATCTGGTGATGT | 23072 |
rs267601513 | snp | A/C/G | 1.65682e-05 | 0.00287817 | HECW1 | 7 | allele_origin=G(germline)/A(somatic) | 7:43479740 | GAAGTTACAGCGCTG[A/C/G]AGAGGTAACCCTCCC | 23072 |
rs267601514 | snp | A/G | | | missense | HECW1 | GRCh38.p7 | 7:43561876 | TACTCCATGTTGTAT[A/G]AAAAGCTGTTAACAG | 23072 |
rs367544933 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412442 | TTATTTATTTATTTA[C/T]TTATTTATTTATTTA | 23072 |
rs367552202 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43228499 | ACCGTCAGGAGGTGC[A/G]AAGAACTATGGGAAC | 23072 |
rs367557051 | snp | C/T | | | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512326 | ACGCCCTGCCCACCT[C/T]CCTTCACTCTGGAAT | 23072 |
rs367564490 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556115 | ATCAGAGGAGCACAG[C/G]GGGTAAGAGCAGCGT | 23072 |
rs367572727 | snp | C/G/T | 6.62431e-05 | 0.00575481 | missense | HECW1 | GRCh38.p7 | 7:43552240 | GTAGACTCGAGGCTG[C/G/T]TGTCCGTGTTTGATG | 23072 |
rs367579167 | snp | C/T | 4.99463e-05 | 0.00499707 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43501240 | AGAGATTATGTCCTA[C/T]GTCCCCCTGCAGGCT | 23072 |
rs367579373 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43177479 | TTTCAGTGTATTCCC[C/T]ACAGTCATCTTTCCC | 23072 |
rs367582714 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43502134 | GGAAGAGCCCTTTCT[A/G]AAACATTCTGCCTTG | 23072 |
rs367595685 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213509 | GGAGTGTAGTGGCGT[A/G]ATCTCGGCTCACTGC | 23072 |
rs367630673 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43236991 | ATAGTAAATGAAACC[-/A]AAAAAAAAACTAACT | 23072 |
rs367635257 | in-del | -/CA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43340290 | AGCAGAGCAGTCTCA[-/CA]GCTCACTGCAACCGC | 23072 |
rs367660376 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43407807 | AGCCCTCCTCCTTCC[C/T]TCCATTCATGGAGCC | 23072 |
rs367661051 | snp | A/G | 6.62932e-05 | 0.00575693 | missense | HECW1 | GRCh38.p7 | 7:43508080 | TGATGGCCTATTCGC[A/G]GAAAGAGCTCCAGCG | 23072 |
rs367669924 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43549110 | CGGACAAAGGAACAC[A/G]CAGCCCATCCCTTCA | 23072 |
rs367670483 | snp | A/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520595 | GCACCTTCTCAAGAC[A/T]AATATGTTCATCTTC | 23072 |
rs367672434 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110892 | CTGCTCTACAAGGCT[C/T]CTTTATCTACTCAGG | 23072 |
rs367686681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125427 | TTTTGATTCAATAAC[A/G]ATATATATTTTCTAT | 23072 |
rs367711735 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43503918 | TTCTAGTTCTGTGTA[C/T]ATCCCAAAACCTGGT | 23072 |
rs367751392 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43113483 | CGCGTGGCCAGGTCC[A/G]GCCCTTGCTCCCATG | 23072 |
rs367763989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149091 | AGATGAATGCTAAAA[A/T]TAGAAGCTAAAAAGT | 23072 |
rs367765492 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189021 | CCCACAGGGTGAGGC[A/G]CACTCGGCTAATCTT | 23072 |
rs367772904 | snp | G/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298608 | CAGTGTGTGAGGCAT[G/T]AAGACTCAGTAGCAT | 23072 |
rs367774344 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119982 | GAAGTCTTCTCATTC[A/C]TTCATTCATTCAACA | 23072 |
rs367776015 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43341091 | GCATGTTCTCACTCA[C/T]AGGTGGGAATTGAAC | 23072 |
rs367776617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43265737 | AGGCACATTCTCACA[A/G]GGCTGCTCCCACTTC | 23072 |
rs367790007 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43534163 | AGAAGGCTTTTAAAG[G/T]CTTTTCTTTCACTAT | 23072 |
rs367791286 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127858 | AGATCATTGATGAAG[A/G]TGGCTACATTAAAAA | 23072 |
rs367791438 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43164832 | GCCGAGCATGCAGCC[A/G]CGCTTCCATGGTGTA | 23072 |
rs367809687 | in-del | -/TCACCTGGAGATAAATCGCAGTGCCTGGCCG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422899 | CCTGGCCGAGAGTCG[lengthTooLong]AGAGTCGTGGTCTCC | 23072 |
rs367830766 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413274 | GAAGTGTCTGTTCAT[A/G]TCCTTCGCCCACTTT | 23072 |
rs367832153 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43554947 | GTGAAGGTGAGGTGG[C/T]TGTGAGACTTGCACT | 23072 |
rs367834987 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488503 | AGAAAGAAAGAAAGA[-/G]AAAGAAAAGAAAGAA | 23072 |
rs367842966 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187900 | CAGTCCCAGACTGAA[A/T]TTTTTCACATGTGCA | 23072 |
rs367849144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43431490 | GCCACCCTTTTCTCC[C/T]TGCCTGCTAGTCTCC | 23072 |
rs367856687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43420595 | ACATTACCCAAACTA[C/T]CCAAATTAGTGAATT | 23072 |
rs367876671 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307899 | ATATATATATATACA[C/T]ATATATATATATATA | 23072 |
rs367879190 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416520 | AGGTGGGGCCTACAG[A/T]GGCAGGCAGGCCTCC | 23072 |
rs367919227 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281596 | CTCTTCTTTCTCTCA[C/G]TCCACTCTCCCTCAA | 23072 |
rs367924457 | snp | A/G | 6.62855e-05 | 0.00575659 | missense | HECW1 | GRCh38.p7 | 7:43320695 | TCAATGGTTCTCATC[A/G]GGGCCAGATCATCTG | 23072 |
rs367924597 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506543 | ACTGAGAGAGTGATG[C/G]AAATGAAGGGCTTGT | 23072 |
rs367929468 | snp | C/T | 1.65839e-05 | 0.00287953 | missense | HECW1 | GRCh38.p7 | 7:43561859 | TTCCACCGTATCCCT[C/T]GTACTCCATGTTGTA | 23072 |
rs367930122 | snp | C/T | 6.65347e-05 | 0.0057674 | missense | HECW1 | GRCh38.p7 | 7:43456437 | CAGCAGATGGAGCAA[C/T]TCAACAGGCGGTTGG | 23072 |
rs367931665 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43427648 | TTCTGTAGGTCAGAA[A/G]TCTGGGCACAACCTG | 23072 |
rs367937946 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198402 | CACACTCATCAGTCA[C/T]ACACCCATACTCTCT | 23072 |
rs367942802 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43446978 | GACATTACTCGATAA[C/T]TACAGCATAATTAAA | 23072 |
rs367947817 | snp | A/G | 1.67211e-05 | 0.00289142 | missense | HECW1 | GRCh38.p7 | 7:43444400 | CCAGGGAACCAAAGC[A/G]TAGAGCTTTCCAGAC | 23072 |
rs367948558 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43218406 | TCATGGATCTGAACA[A/C]AGCAGTGGTTTAGGA | 23072 |
rs367958385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43240737 | GAGTAGTGACAGGCC[A/G]TGTCAGATGGTTGAT | 23072 |
rs367962918 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343352 | GTGTACATGTGCCAT[A/G]ATGGTTTGCTGCACC | 23072 |
rs367966138 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43483918 | GGCAAAGAGCTATTC[A/G]AGAGAGGCCTGCTAG | 23072 |
rs367966826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43389262 | ACCGCCAGCGTCAGC[A/G]TCACCTGGGAACTTG | 23072 |
rs367968659 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43356181 | CTTCAGCTATAAAGA[C/T]ACATATAGACTGAAA | 23072 |
rs367970441 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43534898 | TGATGTAAGAAACTA[G/T]ACATGCCAGTCTATG | 23072 |
rs367972356 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416871 | CAGGTGAGGCAATGC[C/T]CGCCCTGCTTCGGCT | 23072 |
rs367975595 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515848 | AGAAACTACCAAGTT[A/G]AAATGCTCGCATATT | 23072 |
rs367994771 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43501671 | CCCCTTCTCTACAAA[A/G]AAATTAAAACTAAGC | 23072 |
rs368003146 | in-del | -/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43181045 | CACTATTCTACTCTC[-/TT]CTTCTATGAGATCAA | 23072 |
rs368011857 | snp | C/G | 1.65603e-05 | 0.00287747 | missense | HECW1 | GRCh38.p7 | 7:43479685 | CAGAACGGTCGTCTT[C/G]CCAATCATCTAACTC | 23072 |
rs368013578 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327139 | ATAAATACTTGGGCC[A/G]TAGGCGCTAAGCCCT | 23072 |
rs368015377 | in-del | -/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43338710 | CAGAAAGGGAACTCT[-/TT]CACGTAAACAGCGCT | 23072 |
rs368017805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43258256 | GCTAAGGCATGAGAA[C/T]CGCTTGAACCTGGGA | 23072 |
rs368018953 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224321 | GCATCTCTAAGTTCA[C/T]AGCCTAGTGGAGGCA | 23072 |
rs368019811 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43286993 | TTTGCTGTGTCCCGG[A/G]CATTGTTTAATGATG | 23072 |
rs368026825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43322151 | CTCGGCTCACTGCAA[C/T]CTCCGCCTCCCGGGT | 23072 |
rs368028468 | in-del | -/AAAGGAAGGAAG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247731 | GAAGAAGGAAGGAAG[-/AAAGGAAGGAAG]GAGGGAGGGAGGAAG | 23072 |
rs368040886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43281752 | TTTAGAGAGACAAGG[A/T]CTAACTATGTTGCCC | 23072 |
rs368043641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43432788 | ATAATTGCCAATTAA[A/T]TATTTCCTTTAGTTA | 23072 |
rs368044025 | in-del | -/ACAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198777 | CACACTCTCTCACAC[-/ACAC]TCCACACTCACGTGC | 23072 |
rs368052401 | in-del | -/ACA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128913 | GGAATGGAAATAACA[-/ACA]GAACTAGAATTGGAA | 23072 |
rs368058513 | in-del | -/CTA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43404350 | CGTTTTCTAAAGCTA[-/CTA]ATTCTCCCAAAGCTA | 23072 |
rs368069301 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308224 | ATATATTATGATATA[-/T]TTTTATATAATAATA | 23072 |
rs368085361 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413176 | TGGTATCTCATAGTG[C/G]TTTTGATTTGCATTT | 23072 |
rs368106901 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529675 | CCCAACCTTAACACC[C/T]TCGCTGGAGTCCATT | 23072 |
rs368117572 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43277138 | GAAAGAGAAATCAGT[A/T]CATTCATTAGGTAAA | 23072 |
rs368119246 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237150 | AAGGAAGTAGGTAGG[A/T]AGGTAGGTAGGTAGG | 23072 |
rs368136033 | in-del | -/AACA/ACAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43383828 | GAAGCCTTGCCAGTA[-/AACA/ACAC]ACAGTTGATTAACAT | 23072 |
rs368153264 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156676 | GTGCCAGTCCTTAAT[A/G]TTGTACCAGATGTTT | 23072 |
rs368156351 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161173 | AAAGAATCTGAATTA[C/G]TGTCACTTTTTCAAG | 23072 |
rs368160069 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43236307 | ATTATTAAGTGATTT[G/T]GGAAACCATTCATGG | 23072 |
rs368160373 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43170534 | AAGGGGTTAGTCACC[A/G]TAAGGTTACAGCTCG | 23072 |
rs368167810 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124400 | CAGGCAATGAGCTCA[A/G]TGAGATTTGAAAATT | 23072 |
rs368174841 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140619 | CTAGTCTTAAATTAC[A/G]TGATTCAATGATTCA | 23072 |
rs368179030 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43212967 | TCTAAGATTATGACA[A/G]AAGTATATTTAAAGC | 23072 |
rs368182508 | snp | A/G | 0.000115922 | 0.00761233 | missense | HECW1 | GRCh38.p7 | 7:43552313 | ACCTAAATGACTGGC[A/G]GAATAACACTGAGTA | 23072 |
rs368183835 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43547830 | CATTAGTGGCCCTTC[A/G/T]TGTGGGTCCCACAAT | 23072 |
rs368193410 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128318 | TGTTAGGGGCTAATG[C/T]AGCTGGTGACTAAGT | 23072 |
rs368197745 | snp | A/C | 0.000150345 | 0.00866889 | intron-variant | HECW1 | GRCh38.p7 | 7:43438152 | CGCCATAGGGTAAAC[A/C]TGTGACTGAGATCTT | 23072 |
rs368218332 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43451748 | ATTCACTTGGCATCA[C/G]ATATGTTCATGAATT | 23072 |
rs368220658 | snp | C/T | 0.00113735 | 0.0238198 | intron-variant | HECW1 | GRCh38.p7 | 7:43552369 | GTAATGATGCAATGA[C/T]CACAAATAGAACTCA | 23072 |
rs368221603 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43196123 | ACTGCCGCCTGGAAT[A/T]TTCCAATCTCCTGCA | 23072 |
rs368223664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43557363 | AGAGCGCCAGACACC[A/G]CCACAGCAAAACCCG | 23072 |
rs368223993 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523214 | CTCCATGTTGGCCGG[-/TG]GGGGGGTCTCGAACT | 23072 |
rs368228440 | in-del | -/AA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43499469 | GCAAGACTCTGTCTC[-/AA]AAAAAAAAAAGAAAG | 23072 |
rs368228857 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43525033 | AATAGGGATTAAAAA[G/T]TATGCTTTATTTGTT | 23072 |
rs368231195 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281146 | CTCCGCCCACCCAAG[A/C]AAGTGGCAAAGAGCA | 23072 |
rs368235881 | snp | A/G | 0.000163987 | 0.00905353 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43508129 | CTTTGTTGGAGAGGA[A/G]GGGTGAGGCACCAGG | 23072 |
rs368244752 | snp | C/T | 9.93921e-05 | 0.00704884 | missense | HECW1 | GRCh38.p7 | 7:43311959 | CTGACCTGGTCACCT[C/T]GGACAGCCGCTCCAC | 23072 |
rs368249231 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137828 | ATGTTGGGATTACAG[A/G]CATGAGCCACCGTGC | 23072 |
rs368256823 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant, nc-transcript-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512063 | AGCTGCTGCTGATCT[C/G/T]GGGTCGGTGTCAGGT | 23072 |
rs368260706 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140627 | AAATTACGTGATTCA[A/G]TGATTCAATATATCG | 23072 |
rs368260823 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43364525 | ATGTATAGAGAAAGC[C/T]GTGACCAGGCACCTG | 23072 |
rs368261346 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210749 | CAAGCCTTTAGCCCA[A/G]TCCAGAGCAGCAATG | 23072 |
rs368262630 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43526603 | AGGCACTCTGGGTTC[C/T]GCCCGGAACACAATG | 23072 |
rs368265152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43321538 | CCTTCAGTCCACAGC[C/T]CCTTCTCCTCCACTT | 23072 |
rs368269884 | snp | A/G | 4.96882e-05 | 0.00498414 | intron-variant, missense | HECW1 | GRCh38.p7 | 7:43450864 | ATTCCCAGCCAGTAA[A/G]CCAGCTTCCTTCCCT | 23072 |
rs368272120 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43241265 | TGTGTGGACAGGTCA[C/T]TTGGTCCCCATCTGA | 23072 |
rs368272389 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43175152 | TTCATGTTTTTTTTT[-/T]GATGTACAACACGAT | 23072 |
rs368278470 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43401180 | ATTATTCTGTCTACC[A/G]CAGTCAAGAAGAGAT | 23072 |
rs368302069 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43468259 | CAATCCCCAGAGGCC[C/T]TAAATTAATGCTCCC | 23072 |
rs368305061 | in-del | -/TC | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43349004 | TGTTGAATGAAATGT[-/TC]TTTTTTTTCTTCGTT | 23072 |
rs368313535 | snp | A/G | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112462 | GGCCGGCGGTAACAA[A/G]AATCGATATATATTT | 23072 |
rs368339794 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43561600 | GGTTTGCTTGCAAAT[A/G]CAAACAACCCATTTT | 23072 |
rs368367901 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556450 | CTAGCACTGTGGGAG[G/T]CTAAGGCAGGCGGAT | 23072 |
rs368390579 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192754 | GATATCTTTCCCCAT[A/C]TGTTAAGGTTGTACA | 23072 |
rs368395667 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43169835 | TGTATCTTAAACACA[A/T]CTCATCTTCCTCCTC | 23072 |
rs368413920 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358896 | ATGGCGTGATCTTGG[C/T]TCACTGCCACCTCCA | 23072 |
rs368422121 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43421034 | GACTTTTATACTGCC[A/G]GATGTCCAGATAAAA | 23072 |
rs368430680 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43258963 | TTGTTTTTGTTTTTA[C/T]CAATTCAACTCTTAG | 23072 |
rs368438768 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43543550 | TTGGAAGGCTGAGGT[A/G]GGCAGATCACCTGAG | 23072 |
rs368446459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43540422 | GTTTAGGAGCAGGCA[A/G]CAATGGAACCAAGCC | 23072 |
rs368446743 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43430769 | ACTGTGGCCTCCATT[A/T]TTATTTTTCTTTATT | 23072 |
rs368470705 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361974 | TGGTGAAACGCTGTC[G/T]CTACTAAAAATACAA | 23072 |
rs368472154 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43443653 | GACCTTGTTTTTTTT[A/T]AATTGGAATAAACTC | 23072 |
rs368485190 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43219741 | GATTAAGTCAGGGGT[C/T]GATCTTTAATTACCA | 23072 |
rs368493574 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43288269 | GTAGAGTCACAGGAG[A/C]TCTTGCAAATTAGAC | 23072 |
rs368494869 | snp | A/G | 8.30213e-05 | 0.00644234 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43438005 | TCTTTCATTGCAGCA[A/G]TTCAGTTTTGTGTCC | 23072 |
rs368497230 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508844 | CATTCACTCCAAAGA[C/G]CAGAGGCTGCTCTCT | 23072 |
rs368501997 | in-del | -/TA | 0.166506 | 0.235645 | intron-variant | HECW1 | GRCh38.p7 | 7:43308289 | ATTATATGATATATT[-/TA]TATATATTATATGAT | 23072 |
rs368513147 | in-del | -/TATATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307877 | TGGTAATCATTTCAC[-/TATATA]TATATATATATATAC | 23072 |
rs368518902 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43342154 | TTTACCTTAAGGAGA[A/C/T]TCAACAGGTAATATC | 23072 |
rs368523352 | in-del | -/GTTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43216144 | TTTGTTTGTTTGTTT[-/GTTT]TTGTTTTTGTTTTTT | 23072 |
rs368530386 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412925 | ACATACGTGTGCATG[G/T]GTCTTTATAGCAGCA | 23072 |
rs368530939 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327851 | TGTGCTAATGGGATG[A/T]AGAAAGAACATAATA | 23072 |
rs368555124 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303097 | TCCCTCTCCCACACC[C/T]ACAGCCCCCTGCCCA | 23072 |
rs368558943 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140181 | TGACATCCTTTTTTG[G/T]CTCTGTTTCATCTAT | 23072 |
rs368559724 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43282783 | TATAGAATCAATATT[A/T]TGCTTCACAGCATGA | 23072 |
rs368560425 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43478419 | TGAGAGTGAAACTCC[A/G]TCTCAAAAAAAAAGT | 23072 |
rs368561030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43262608 | CAAAAACTAAGCTAT[A/G]AAAAGTAGTTTTCTC | 23072 |
rs368562868 | snp | A/G | 3.31192e-05 | 0.00406921 | utr-variant-5-prime, intron-variant | HECW1 | GRCh38.p7 | 7:43243885 | CCCAGGAATTGATGC[A/G]CGTACACGTGGTGGG | 23072 |
rs368573432 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43167956 | ACTGTAAGCCCAGCA[C/T]TCCTGAATACTCACA | 23072 |
rs368582672 | snp | A/G | 3.31362e-05 | 0.00407026 | intron-variant | HECW1 | GRCh38.p7 | 7:43500690 | CCTCTTCTTTCTCAC[A/G]TGATTCAGGGAGAAA | 23072 |
rs368584075 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214292 | AGAAATGTGAAAGGA[A/G]ATTGTAACTGTCCTT | 23072 |
rs368585257 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43275268 | TTCTCCTAAGACTAT[C/T]TAATAAAATAAAAAT | 23072 |
rs368589881 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43466734 | CGTGAGTCTCCCAAA[A/G]AGGAAAAAGGCTGGA | 23072 |
rs368590802 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43561180 | CTGGCCATGCAGGAG[A/G]AAGCACATGAAGCAA | 23072 |
rs368600507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43251637 | TCTAGTTTCTTTCTA[C/T]TTATTATATTCACAG | 23072 |
rs368606583 | snp | A/C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43432240 | CGCCTCCCGGGTTCA[A/C/T]GCCATTCTCCTGCCT | 23072 |
rs368613090 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43364226 | TTAATTTTCTGAGCA[C/T]TGTATGGTCTCACGA | 23072 |
rs368616989 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43338050 | GGCAACTCAGTCCTC[C/T]ACCATCTGACCAGCC | 23072 |
rs368618017 | in-del | -/AGAA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247977 | AAAAAGAGAAAGGAA[-/AGAA]GGAAGGAAGAAGGAA | 23072 |
rs368640174 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347130 | CATCCATGAGCTTGG[G/T]ATGTGTTTCCATTTG | 23072 |
rs368649954 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43411507 | GTCAAGGTGGTTGAC[A/T]GAGTTGTAGAGATTC | 23072 |
rs368650141 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350222 | TTGTAGGGTTTCTGC[C/T]GAGAAATCTGCTGTC | 23072 |
rs368656082 | snp | C/G/T | 0.000343185 | 0.013095 | intron-variant | HECW1 | GRCh38.p7 | 7:43312116 | GCCAAGTGTATTATT[C/G/T]ATAATTCACTTTTAC | 23072 |
rs368666210 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154218 | TATTAATAATTTCTA[A/G]CATTTCTGCATTGTG | 23072 |
rs368668229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43537133 | AGACTCCTGAGATCC[A/G]TGGAGAGAAAGAAGT | 23072 |
rs368670451 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529196 | GTTCCCACCTCCTCC[C/T]CCTACCATCGCTCCT | 23072 |
rs368679734 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126697 | GCAAGTCTATCGGTG[A/C]CATTTTTTCCAACAG | 23072 |
rs368684213 | in-del | -/GTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361058 | TGTTCTTGTGCGTGC[-/GTGT]GTGTGTGTGTGTGTG | 23072 |
rs368687499 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43420562 | AGATAACATTGTTGT[A/G]TCAGTAAACAGTACA | 23072 |
rs368688420 | in-del | CCCCCG/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237832 | CAATTCACCAGTCTT[CCCCCG/T]CCCCCCCGCCGCCCC | 23072 |
rs368709795 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | HECW1 | GRCh38.p7 | 7:43243844 | TTGCTTGGGATACAC[A/G]CTAAGTTAACCTCGT | 23072 |
rs368719054 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129005 | GAGTTGCTTCTTATG[C/G]ATGAGCAAGGAAAGT | 23072 |
rs368720880 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43322139 | CAATGGCACAATCTC[A/G]GCTCACTGCAACCTC | 23072 |
rs368735442 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43405075 | CTGACAATCTGTAAG[A/C]CTTCATTTTCTCTTT | 23072 |
rs368736614 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43371364 | CACTCTTATGTGGAA[C/T]GTTGGTAGTTGGGGA | 23072 |
rs368760306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43282060 | TCAGATATTAGTTGT[A/G]CAGCTATTTAGTTAC | 23072 |
rs368768711 | snp | A/G/T | 1.67973e-05 | 0.00289799 | missense | HECW1 | GRCh38.p7 | 7:43445270 | AGCTCGTGCTACAGC[A/G/T]CCTCGTGCTACAGCC | 23072 |
rs368769722 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43206442 | TCTGCTCTCTATTGG[A/C]TCAAACATATTTTGT | 23072 |
rs368771064 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43484180 | ATGGGTGACCACTAA[C/T]GTGTGTTCCAGCTGT | 23072 |
rs368790828 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43554409 | TAAATCTGCTCTTGT[C/T]CTAAAACTTGACCTG | 23072 |
rs368798804 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213681 | CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 23072 |
rs368815970 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43266814 | TATATTCTATTTAAA[A/G]GAGACACGCAAAAGG | 23072 |
rs368818412 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43271586 | AGCCAAATTAAGAAT[A/G]CAATCCAATTTACAA | 23072 |
rs368818763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43464915 | CAAACAGTCCTCCCA[A/G]CACAGCCTCCTGAGT | 23072 |
rs368830262 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512572 | TATATGTTATCATAA[C/T]CATTAATAAAAATTA | 23072 |
rs368844639 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43216562 | TAAGCTGAAGATGTT[A/G]CCTGGTACTGCTCCC | 23072 |
rs368846910 | in-del | -/TTTAT | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43330983 | TTATTTATTTATTTA[-/TTTAT]TTTATTTTATTTTTT | 23072 |
rs368855791 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43207132 | GCTCACTGCAACCTC[C/T]GTCTCCTGGGTTCAA | 23072 |
rs368858456 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287998 | TGGAGGTGGGCTTGA[A/G]ATGCATATTAGATAT | 23072 |
rs368861282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43490932 | CTGGCTTATTTTTAG[A/G]TTTTTAGTGGAAATG | 23072 |
rs368879596 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43382158 | GGGCATGGTGGTGGG[A/G]GCCTGTAGTCCCAGC | 23072 |
rs368880458 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43355292 | CCAGGATACTCTAAT[A/G]CTGTAATTGTGGTGT | 23072 |
rs368888011 | snp | C/G | 0.000155988 | 0.00883004 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445287 | CTCGTGCTACAGCCC[C/G]TCCTGCTACAACGGC | 23072 |
rs368890093 | snp | C/T | | | intron-variant, upstream-variant-2KB, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113736 | CTACCCCCACGTTCC[C/T]GGGCGGTGACAATGC | 23072 |
rs368893951 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43553384 | GTATAGAATGAAAAC[C/T]GCTGTCTGCCTAGCT | 23072 |
rs368898407 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43203705 | TCAAATGATCCACCC[A/C]CCTCAGCCTCCCAAA | 23072 |
rs368898758 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524212 | CTTAGATGTTAGCAG[C/T]GTCAAGAGTCTTTCA | 23072 |
rs368901640 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556563 | CATGGTGGCATGCAC[C/T]GGTAGTCCCAGCTAT | 23072 |
rs368904678 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43486712 | ACACCATTGCCTATG[C/T]ATCCATTGTTGACTG | 23072 |
rs368943670 | in-del | -/TTTTC | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43554388 | TTTATAAAATGACTA[-/TTTTC]TTTTCTAAATCTGCT | 23072 |
rs368966573 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43436583 | CACAAGGTGCTCAGT[G/T]GGGGAGCTTCTGAGC | 23072 |
rs368972324 | in-del | -/TTTA | 0.473726 | 0.111565 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137528 | TGCTTTCTGCCTTCT[-/TTTA]TTTATTTATTTATTT | 23072 |
rs368974637 | snp | A/G | 8.28205e-05 | 0.00643455 | missense | HECW1 | GRCh38.p7 | 7:43456372 | CAACCACCTGGCAGC[A/G]TCCGACGGCAGCAGC | 23072 |
rs369007208 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335772 | CTTTCTTTCTTTTTT[C/T]TTTCTTCCTTTCTTC | 23072 |
rs369007700 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377060 | TAGTCTGACTTGTAA[G/T]CAGGTGAATGAATGT | 23072 |
rs369010655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119481 | TTAAATGCGGGTACG[A/G]GGATTCCCCAGGCCT | 23072 |
rs369010775 | in-del | A/GAG | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513855 | TTCAGGCCAAAGAGA[A/GAG]AGAGGAGTTAGAGTC | 23072 |
rs369017594 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43526512 | TTTTTTAACCTGACT[C/T]AGATTTATGGAAATA | 23072 |
rs369021251 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43274051 | AGACGGGGTTTTGCC[A/G]TGTTGACCAGGCTGG | 23072 |
rs369026049 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43473692 | AAGTTATGCTAGTTG[C/G]GCTCAAGGGGAGTAA | 23072 |
rs369028658 | in-del | -/GT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134389 | AGAGAGTGAGACTCT[-/GT]CTCAAAAAAAAAAAA | 23072 |
rs369036889 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163141 | TCCCAAAGCCTTTTG[C/T]TGTATCCCATCTGTG | 23072 |
rs369043163 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328716 | ACAGCCAGAAAGATA[C/T]AACCGGAACATTCCA | 23072 |
rs369044778 | in-del | -/CT | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43254365 | GGCATGGCCCAGTAA[-/CT]CTATATTGTAGCACT | 23072 |
rs369048244 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43288944 | GGGGATATCCAGGTG[C/T]GCTATACGCAGTCAA | 23072 |
rs369049855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43245258 | AGCCTTGATTTCCCC[A/G]GTTCACTCAGCTTAC | 23072 |
rs369050138 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43221614 | GCTGGAGTGCAGTGG[C/T]GCTATCTCGGCTTAC | 23072 |
rs369064607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43467381 | AGAAAGGATGCACCC[A/G]TGAGGAGGCCTGGGG | 23072 |
rs369064827 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359123 | GAGCCACCGTGCCCG[A/G]CCCATATCTTTTAAC | 23072 |
rs369076871 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347347 | GTTGATGTATAGAAG[A/C]GGTACTGATTTGTGT | 23072 |
rs369078676 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372006 | TTTGTATTTTTAGTA[A/G]AGATGGGATTTCACC | 23072 |
rs369083287 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43362854 | TTCACTGAATGAGGC[A/G]GACACAAGGATCCCT | 23072 |
rs369088513 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43417756 | AGTTTCCAATAATAA[A/T]TCTATAATGATTTAA | 23072 |
rs369092684 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347481 | CAAACAGTGACAGTT[C/T]GACTTCCTCTTTACT | 23072 |
rs369097486 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43476740 | GTGAGCTCTCTGAGA[A/C]AACTGTCAAACTACA | 23072 |
rs369107746 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494425 | ACCAGAGTTACCTAC[A/G]TAAAGCATAGATTAA | 23072 |
rs369108690 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43418734 | AAGTTAATATTTTCC[C/T]TTACCACACTGGATA | 23072 |
rs369135763 | snp | A/C | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516065 | TAAAATAGTGCATCC[A/C]TTTATAATTTTCCAA | 23072 |
rs369135906 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43495255 | TCTCCTAATGCTATC[C/T]CTCCCCTAGCCCCCA | 23072 |
rs369141413 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145629 | GCAGAGGTGTCTTCC[C/T]GCTGTAGAGGTCTAG | 23072 |
rs369152042 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43323989 | CAGTGAGCCGAGATC[A/G]CACCATTGCACTCCA | 23072 |
rs369153082 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43178142 | CTCCAAAGTAGCTGG[A/T]ACTACAGGTGCCCAC | 23072 |
rs369163819 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43389739 | TTGAACTCCTGGGCT[C/T]AAGGGATCCTCCTAC | 23072 |
rs369191249 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43362310 | TAAGGTAAGCAGGCC[C/G]GAGGCCCAAAGCCTG | 23072 |
rs369194610 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487984 | AGAGAGAGAGAGAGA[A/G]AGAAAAAAGAAAGAA | 23072 |
rs369198880 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43549823 | GGCTGTTAAGAATTT[G/T]CTGTCATTGAGATTT | 23072 |
rs369209094 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198444 | TCACATTCACACACT[C/T]ACCCACCCTAACACG | 23072 |
rs369215994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43200144 | CAGTTAACTTTCAAA[C/T]GGATTTGATTGGCCC | 23072 |
rs369217277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214828 | GTGAGGGAACCATGT[A/G]GGGGCATGTTCTGAC | 23072 |
rs369219881 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43312707 | AAACAAATTATGCAA[A/T]TAAGTTGGATGCTGA | 23072 |
rs369228101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43235629 | CTCCTGGATGGGATA[A/C]CTTAATGTGCAAAAC | 23072 |
rs369230845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43317604 | CTAGTAACTTTTCTA[A/G]CAACTGGTAACAAAT | 23072 |
rs369250931 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43349184 | GGATTACAGGCATGC[A/G]CCACCACGCCCGGCT | 23072 |
rs369255800 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43203120 | GCGATCTGCCTGCCT[C/T]GACTTCCCAAAGTGC | 23072 |
rs369259091 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43203106 | CGCGTGACACTCAGG[C/T]GATCTGCCTGCCTCG | 23072 |
rs369263189 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43258367 | AAAAATAAAAAAAAT[A/T]AAAAAATAAAAAAAA | 23072 |
rs369264179 | in-del | -/CTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43306296 | CTTCCTGATTTCTGT[-/CTGT]TTTGTATTTTCCTAT | 23072 |
rs369264225 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43335540 | TGATCCACCAGCACC[C/T]TGACATTGAACTTTC | 23072 |
rs369265302 | snp | A/T | | | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563336 | TAAACCCAACCATAA[A/T]GGTCATTTGCTATTT | 23072 |
rs369265905 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43352462 | TCTGAATTACCTAGT[A/G]CATTATTACTGAAAG | 23072 |
rs369272184 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43321370 | AATAAATCATTATCA[C/G]AGTTATGGCAGGCTT | 23072 |
rs369281932 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319379 | GGCCTGGGCGACAGA[C/G]CGAGACTCCGTCTCA | 23072 |
rs369284858 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283459 | ATTTTGGAAAATGTA[A/T]TTATTTTGCATAAAA | 23072 |
rs369296597 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43216126 | GGTGAGATGAAGCAG[A/G]TTTTTGTTTGTTTGT | 23072 |
rs369308621 | snp | G/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299501 | TCCGTGAGTTCAAAG[G/T]TTCCAAGTTTAGTCC | 23072 |
rs369319816 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43279452 | AATTGCAAATCCTCT[C/T]GGTGAGCTGCAAGGT | 23072 |
rs369330864 | in-del | -/TAGGG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43219184 | GTTGCCAGGCACATG[-/TAGGG]GCAAGGGCAAGAGGA | 23072 |
rs369340683 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43278787 | TCACCCCTAGGAGGT[C/G]TTTCCTGACCACCGC | 23072 |
rs369348156 | snp | C/G | 1.6748e-05 | 0.00289374 | missense | HECW1 | GRCh38.p7 | 7:43445357 | AGCGCCAAGATCTCC[C/G]AGAGCACGGTCTTCT | 23072 |
rs369349011 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376663 | TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGGCTG | 23072 |
rs369371535 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43338418 | TTCTTGATCCTCTAT[A/G]TATGTTTGTTTTCTG | 23072 |
rs369373354 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43309625 | TCATGAATGCAAATA[C/T]ATCCTACTCAATCGT | 23072 |
rs369374837 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43485909 | ACATGTTTACAATGC[A/G]CAGGTTTGTTACATT | 23072 |
rs369379706 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43536155 | GTTGTTGTTGTTAAA[A/T]GTGGGTTCTTGGTAT | 23072 |
rs369380779 | snp | C/T | 0.000123567 | 0.00785927 | intron-variant | HECW1 | GRCh38.p7 | 7:43311609 | CTGCAGCCTTTGTCA[C/T]GAGGAAGATGCTCTA | 23072 |
rs369382039 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138326 | TATGCTGATGATTAA[A/G]TATCTCTTTATTAAA | 23072 |
rs369387506 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43209863 | ATCACAAGATGGGCC[A/G]GGCATTGGCGTTCAC | 23072 |
rs369388196 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159067 | CACAGCCTGAGAACT[A/G]CTGCAGTAAACATTC | 23072 |
rs369389859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43384806 | CTCTATGCAAAATGC[A/G]GCCCTTGTCTTCACT | 23072 |
rs369402221 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150744 | GCTTTGTGATCCTCC[A/G]CCCAGTACAGGCACA | 23072 |
rs369406998 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162776 | AAGCTCCCATACTAC[A/T]GTAATAATAACATTG | 23072 |
rs369417684 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119140 | TCTTATTTGAAGCTA[C/T]TTTTGTGTTTCTGCC | 23072 |
rs369422385 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43217602 | CTAATTTCAAATGAC[C/T]GTAAAAGGGGGAAGA | 23072 |
rs369424007 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126193 | TGCTCCTTCCCTTTT[A/G]TAATTGTTCTATTTT | 23072 |
rs369426459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43305948 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 23072 |
rs369426934 | snp | A/G | 1.68621e-05 | 0.00290358 | missense | HECW1 | GRCh38.p7 | 7:43550475 | TTGAAGTCTGGAGGA[A/G]CCAACACACAGGTGA | 23072 |
rs369427514 | snp | A/G | 1.70901e-05 | 0.00292314 | intron-variant | HECW1 | GRCh38.p7 | 7:43492220 | CCTGGCTCAAAGAAT[A/G]GCAACACCTAGACTT | 23072 |
rs369433003 | snp | A/C/G | 8.04155e-05 | 0.00634052 | missense | HECW1 | GRCh38.p7 | 7:43444975 | GAAGGATGGGCTCAG[A/C/G]GAGGTGGACACGGTG | 23072 |
rs369442081 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43346546 | ATTTGCTTTTGGGTT[A/C]TTGGTCGTGAAATCC | 23072 |
rs369443108 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264572 | TATTGTCAGCCAGGC[A/G]CGGTGGCTCACGCCT | 23072 |
rs369444533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43177750 | GAAGCTTAGCACAGC[A/G]TCTGGCACAAACACT | 23072 |
rs369457106 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43231843 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAA | 23072 |
rs369474916 | snp | A/G | 1.65627e-05 | 0.00287769 | missense | HECW1 | GRCh38.p7 | 7:43463719 | AAGATTCTGGCAGCC[A/G]AAGCTGCGAGCAAGC | 23072 |
rs369489092 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43235377 | ATACTTGGGAACAAA[C/T]ACTAGACTGATAAAA | 23072 |
rs369492463 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328230 | TACTTGGGAAGCTGA[C/G]ATGGGAGAATCACTT | 23072 |
rs369502320 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43185680 | AAGCATTTTGGCTTG[G/T]TTTTTTTCTATATTT | 23072 |
rs369547429 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43502387 | TTTCGCCAGACACAA[C/T]GGCTAACCCGCGTAA | 23072 |
rs369558928 | snp | A/C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43485121 | CCGAAAAAAAAGCTT[A/C/G]ACAGTGACTGCCTCA | 23072 |
rs369560904 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43349096 | CTGGAATGCAATGGC[A/G/T]CACTCTCGGCTCACT | 23072 |
rs369571790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43320828 | TTCCCGTTGCACTGC[C/T]TCCACTAAGAAATGG | 23072 |
rs369573880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516716 | GGATACCTCTGAGAA[A/G]TGCATCACTAAGCAA | 23072 |
rs369576129 | in-del | AA/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546625 | CAATATCAAAAAAAA[AA/C]AAACAAACAAACTTT | 23072 |
rs369578125 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43554124 | GGGATCTCCTGTTCA[C/T]GAAACTGGCTGTTCG | 23072 |
rs369583430 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134892 | GGATTGTTTTTCTAC[C/T]TGGGTACATTTAAGA | 23072 |
rs369598569 | snp | C/G | 9.96512e-05 | 0.00705802 | missense | HECW1 | GRCh38.p7 | 7:43468932 | CAGAGTGCCTACCGA[C/G]TCTTCACCAGTAGCA | 23072 |
rs369603946 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43357172 | AAAACTAACAGATTC[A/C]TCAAAAAATTAAAAA | 23072 |
rs369613533 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147160 | AGCTAAAGAATAATA[C/G]GTAGTTCCCAGGTAA | 23072 |
rs369624261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43561281 | GAAATGCAGCACTTC[A/G]ACTTTAGGTTCTGTG | 23072 |
rs369630439 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43234180 | ATTCTCACCACCCAC[A/T]CCTCTCCCACCCTGT | 23072 |
rs369632470 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544652 | AAATTACTAATATAT[C/T]AGGATCTTCATCACA | 23072 |
rs369636277 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129878 | CTCAAGATTACTTAT[A/C]ATACCTAATACAATG | 23072 |
rs369643434 | snp | C/T | 1.65693e-05 | 0.00287826 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43507186 | CTACCGAAGAGACTT[C/T]GAGGCCAAGCTCCGC | 23072 |
rs369654096 | snp | A/G | 0.000991216 | 0.0222402 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43360971 | CACGGTCAAAAACTC[A/G]GCAGCTCCTGTAAGT | 23072 |
rs369668930 | snp | A/G/T | 0.000706123 | 0.0187771 | intron-variant | HECW1 | GRCh38.p7 | 7:43311697 | ACATCTTTCGTTTTC[A/G/T]TGTGATGACGGTGAC | 23072 |
rs369681341 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308250 | TAATATATAATATAT[A/T]TATATTATATGATAT | 23072 |
rs369685621 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43479967 | CTTTTGTCCCACACA[A/G]TCACCACTACTAAAA | 23072 |
rs369685851 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260165 | CAATGGAAAGGCATC[C/T]CCAGTTGAGAAAGAA | 23072 |
rs369687862 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43338343 | TTCACTCTTGCCTTC[C/T]ATATCCCTCACCAGG | 23072 |
rs369689714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43314892 | GTGATTTCATCTCAT[C/T]TGTCATTTCATGAAT | 23072 |
rs369689787 | in-del | -/TCCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43353636 | CACAATGCCCCTCCC[-/TCCC]CTCAATCTACCTGGC | 23072 |
rs369691871 | in-del | -/AATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192508 | CAATAAAAATGACTA[-/AATA]CGTAAAGATAAACTT | 23072 |
rs369700215 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43492780 | AGAACTCCTCTTATG[A/G]GAGAGCTATTTTGTT | 23072 |
rs369735393 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378345 | AGGACTTGTCAGGAA[C/T]AGGATTATTCAAGAG | 23072 |
rs369739622 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43405233 | GAGGCAATGGTAGTC[A/G]CTATTTTATGATGAA | 23072 |
rs369747487 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43398056 | GAGGTCAGAAGTTTG[A/G]GACCAGCCTGGCCAA | 23072 |
rs369748135 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43489289 | ATATTTTAAATACAC[A/G]TTAAGGCAAACTGGC | 23072 |
rs369749837 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43489119 | ACTTTCACTCAGGGC[A/G]AAACAACAAATGTTT | 23072 |
rs369751871 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43423175 | ATTCTCTGAAACGCA[C/G]AGCTGGTACTGGTGG | 23072 |
rs369754037 | snp | C/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43463043 | AAGTCCAGCACAGAG[C/G/T]CTGCACACATTGGAA | 23072 |
rs369761230 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43504184 | GATGACTTCAACATC[A/G]ACAGGGACCCTCATT | 23072 |
rs369765123 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546591 | ACTCAAGGGGTTCTG[C/G]GTGGCCAAGGGCATT | 23072 |
rs369768080 | snp | A/G | 6.77794e-05 | 0.00582109 | intron-variant | HECW1 | GRCh38.p7 | 7:43438196 | TCCCACCAACAGGTC[A/G]TGCCCAAAGGTGGCC | 23072 |
rs369770078 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308268 | TATTATATGATATAT[A/T]TATATATTATATGAT | 23072 |
rs369791077 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413378 | CAGATGAGTAGGTTG[C/T]GAAAATTTTCTCCCA | 23072 |
rs369792173 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43453045 | TGTAAACCATTTAAG[A/G]GCTTTGTAAATCACT | 23072 |
rs369814372 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43207809 | CATCTCGTGCAGGAG[C/T]CATGCTTATCTTCTC | 23072 |
rs369833120 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43278567 | ATGGCTCCCAGAGCC[C/T]CAACCATGGCCTCCG | 23072 |
rs369834916 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115162 | TGTTGGAAAGGCAAA[C/T]AATTATAACGTGAAC | 23072 |
rs369839766 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43423808 | AGACTGGAGCTGGAA[A/C]TGGTGCCTCGTTCAT | 23072 |
rs369842245 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43371822 | TTTTGTTGATGGTGG[A/T]TTTTGTTTTGTTTTG | 23072 |
rs369845470 | snp | A/C/T | 1.70197e-05 | 0.00291711 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445422 | GTTCGAGTCGGTACC[A/C/T]GACTCCATGCAGAGC | 23072 |
rs369845605 | in-del | -/CAACAAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328325 | AAAACAAAAAACAAA[-/CAACAAA]AAAAACAAGGGTTTG | 23072 |
rs369849087 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166392 | GCCTGGCCTGGTGAA[A/G]GAGATTGACTTTGAA | 23072 |
rs369849088 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43194821 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 23072 |
rs369849574 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358817 | ATCCTTAAAATATAT[-/TC]TTTTTTTTTTTTTTT | 23072 |
rs369856713 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215811 | ATTTTATTAAATTGA[C/T]GTGTCAAATGCTGAA | 23072 |
rs369860685 | in-del | -/CACA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198772 | ATTTGCACACTCTCT[-/CACA]CACACTCCACACTCA | 23072 |
rs369864147 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43366625 | AACTTTATAATAAAT[C/G]GTCTTGAGCCCTTGT | 23072 |
rs369878270 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43311375 | GTTTGCCTTAAAGAA[C/G]GATAAAATCAGATCC | 23072 |
rs369879964 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43536377 | CTTCCCCCTCCACTG[C/T]CCAGGGGAGGCTCCA | 23072 |
rs369882624 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43245481 | TTTCTTCTTTCCAGG[A/G]CTAGTGTCCTTGGGA | 23072 |
rs369893956 | in-del | -/CTCA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43257054 | GTTATTAGATACTCA[-/CTCA]TCCTTTTCATCATTC | 23072 |
rs369898473 | in-del | -/CT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160828 | TCAGGGACAAGCTCT[-/CT]TTTGTTCATGAGTTT | 23072 |
rs369898795 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43229919 | TTTTTGCCATACTTT[G/T]GATGGCAAAAACCAC | 23072 |
rs369898917 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43318331 | CTTTTTGCAGAAATG[A/G]GGCAATTACTGTAAA | 23072 |
rs369905426 | in-del | -/AAAG/AG/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43553688 | AAAAAAAAAAAAAAA[-/AAAG/AG/G]GTCTCTGCCTGGCTG | 23072 |
rs369908764 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363679 | AATCCCACAGGACTG[C/T]ATTTTCACGGGCAAT | 23072 |
rs369941339 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378816 | CTCAAAAAACAAAAA[-/T]AAAAACAAAAGAAGG | 23072 |
rs369949541 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43272400 | GTGAATAGACAACCT[A/G]CAGAATGGGAGAAAA | 23072 |
rs369959039 | snp | A/C/G | 0.000282692 | 0.0118857 | intron-variant | HECW1 | GRCh38.p7 | 7:43479779 | GCCCTACTGTTCACC[A/C/G]GTCACAGTCTCTGCC | 23072 |
rs369959223 | snp | C/G | 0.00285321 | 0.0376625 | intron-variant | HECW1 | GRCh38.p7 | 7:43361005 | ATTTCTCCGTCTTTG[C/G]TTAGACCTAACTCTG | 23072 |
rs369959491 | in-del | -/TCTTG | 0.00795532 | 0.062565 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148479 | TTTCCATCTAGTAGC[-/TCTTG]TCTTCACTGTGATCC | 23072 |
rs369965476 | snp | A/C | 3.31708e-05 | 0.00407238 | missense | HECW1 | GRCh38.p7 | 7:43463785 | CAGAAGCCGAATCTT[A/C]CCAGTCCAGCTTAGG | 23072 |
rs369966557 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43227462 | ATACTTTAATCACTA[A/G]GTGCAGAAAGTATGT | 23072 |
rs369972320 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43314013 | TTATTGAAATGGAGT[C/T]TCACTATATTGCCCA | 23072 |
rs369978776 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43344840 | AAGTACAGTTTATCA[C/G]AATTTCTCGGATTCA | 23072 |
rs370000752 | snp | A/C | 0.000404372 | 0.0142135 | missense | HECW1 | GRCh38.p7 | 7:43445538 | CGGAAGGTCTGGAAT[A/C]CCCCGTGGCAGGTCC | 23072 |
rs370001018 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43385408 | CTTCTGCCCTCTAAT[A/T]TTGTGATTCACATCC | 23072 |
rs370016372 | snp | A/C/G | | | intron-variant, upstream-variant-2KB, synonymous-codon | HECW1, LOC105375254 | GRCh38.p7 | 7:43113674 | GCCGGGGCGGGGAGG[A/C/G]GGGGGGAATGCGTCC | 23072 |
rs370027674 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43539453 | TGGCACTGTGGTTAT[C/T]GGTCTATTTAAGTTT | 23072 |
rs370029596 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43370826 | AAAGATCAGTGGTTG[G/T]GAAGATTTAGCGGGG | 23072 |
rs370039800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43168390 | CAGCTGGGCATGGTG[A/G]CTCACGCTTGTAATC | 23072 |
rs370041467 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173811 | AAAGACTCACAGTAT[C/T]ACCTCCACCACCCAG | 23072 |
rs370045133 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157826 | TTGGCCTCCCAAAGT[A/G]CTGGGACTATAGGCA | 23072 |
rs370046798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43171634 | AAGGAAAAAAGGGGC[A/G]TTTAGCTCATATCCT | 23072 |
rs370047222 | snp | A/C | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359323 | TATCAATCAAAATAA[A/C]ACTGAGATTCTGTTA | 23072 |
rs370048029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43195433 | CCTCAGGAAGTTGCC[C/T]ACACAGCCACAGGGC | 23072 |
rs370082703 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43182073 | ACAGGCGTGAGCCAC[C/T]GCGCCAGGCCTCTCA | 23072 |
rs370083261 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43339755 | AGAGGGGAGCTCCGC[A/G]GGGTGCAGTCCAATT | 23072 |
rs370106581 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131126 | CAAAAATTAGATGGG[C/T]GTGGTGGCACACGCG | 23072 |
rs370152641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43312885 | AGTCGAGTTATAATT[A/G]CTGGAAGGCCACAAG | 23072 |
rs370153645 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43452879 | GAAGAGCTTTGCAGG[C/T]ACAGGGAATGGCCAC | 23072 |
rs370170018 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494807 | GTGTTAGCCACCTCA[C/G]CCAGCCTAAAGTCAA | 23072 |
rs370194266 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137506 | AATAATATCTTTTCT[C/G]CCTGGAATGCTTTCT | 23072 |
rs370199372 | snp | A/C | 0.000163987 | 0.00905353 | missense | HECW1 | GRCh38.p7 | 7:43479675 | AATCCCTCTTCAGAA[A/C]GGTCGTCTTCCCAAT | 23072 |
rs370202350 | snp | C/T | 1.73999e-05 | 0.00294952 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43541888 | TGTGATTTGAGTGAC[C/T]TGGAATATTTGGATG | 23072 |
rs370206905 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43199090 | ACCCTCCAGACCCTC[A/G]TTGCACACTCTCTCT | 23072 |
rs370207226 | in-del | A/TT | | | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43377642 | GCACAGAAATAACAT[A/TT]TTTTTCTCTTTGTGA | 23072 |
rs370214132 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43528709 | TCACTCCTCTGCCCC[A/C/T]CTGCAGGGCAGATAT | 23072 |
rs370215055 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129022 | TGAGCAAGGAAAGTG[A/T]TTTCTTGAGATGAAA | 23072 |
rs370221950 | in-del | -/AG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488447 | AAGAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA | 23072 |
rs370222820 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141803 | GCACCCGGTGAGATA[C/T]TTGGATTTTAGAAAA | 23072 |
rs370224064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159925 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCTCAA | 23072 |
rs370227718 | in-del | -/TGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43389619 | TCACATTGTTGTTGC[-/TGT]TGTTGTTGTTGTTGT | 23072 |
rs370229656 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43177495 | ACAGTCATCTTTCCC[A/G]TGCTGTCTTCCAGCC | 23072 |
rs370230453 | in-del | -/TA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43276292 | CCATGTCAAGACTCA[-/TA]AGCTCTTTGTGTGTG | 23072 |
rs370231171 | snp | A/C/T | 0.000100922 | 0.00710296 | intron-variant | HECW1 | GRCh38.p7 | 7:43493192 | TCAGGTAAGCCTCGC[A/C/T]CCTCACTCCCTGGAA | 23072 |
rs370237329 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43506384 | AAAGCTGAGAAAAAT[A/G/T]CTCATCCATGTCCTT | 23072 |
rs370248906 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43216773 | GATTCTCCTGCTTCA[A/G]CCTCCCAAGTAGTTG | 23072 |
rs370250375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43238301 | ACCAGAGTGGGTGCT[A/G]TCCAGAAGCTGTCCC | 23072 |
rs370256440 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412804 | TTTTTTATGGCTGCA[C/T]AGTATTCCATGGTGT | 23072 |
rs370262468 | snp | C/T | 1.65905e-05 | 0.0028801 | missense | HECW1 | GRCh38.p7 | 7:43561843 | TTCAACCGACTGGAT[C/T]TTCCACCGTATCCCT | 23072 |
rs370269627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43483617 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 23072 |
rs370274210 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43430090 | TTTCTGAATTTCATA[A/C]ATTTGTGAGTGTGCA | 23072 |
rs370279350 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43331372 | GAGGCGGGCGGATCA[C/T]AAGGTCAGGAGATCG | 23072 |
rs370280305 | in-del | -/TCCTCC | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248697 | TCCTCCTCCTCCTTT[-/TCCTCC]TCCTCCTCCTCCTCC | 23072 |
rs370285400 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43164223 | GCTGGAGACAGGGAG[A/G]CAGCAGAGAAGGCAG | 23072 |
rs370285969 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43450606 | TATTGGACTGTGTGG[C/T]GCAGATCATTAGTTA | 23072 |
rs370302292 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43365458 | GGACATGACATTCCC[A/C]CCCGTGTGGGGCCAT | 23072 |
rs370314193 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139100 | TGTTTCCATCTCCAT[A/T]TTATTATGATATCTT | 23072 |
rs370334619 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298908 | TCTCTGCTGTTTTCC[A/C/G]CATACAAGGTAAAAA | 23072 |
rs370346785 | in-del | -/T | 0.0186012 | 0.0946287 | intron-variant | HECW1 | GRCh38.p7 | 7:43305709 | GGGTTCAAGCGATTC[-/T]CCCTGCCACAGCTTC | 23072 |
rs370365699 | in-del | -/TA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287521 | TTTCTTCTTTGTTTG[-/TA]GAGACAGGGTCTCAC | 23072 |
rs370371148 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43559496 | CACAGGTTACAAAAC[A/G]CATTTATGTGTGTTC | 23072 |
rs370375200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43546911 | TTACTAATAAGGGAC[C/G]TTTGTGGTGCTTTTT | 23072 |
rs370378292 | snp | G/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520545 | ATCCACTTAAAATAC[G/T]GTGTAGTTCATTCAT | 23072 |
rs370379725 | snp | A/G | 3.32801e-05 | 0.00407908 | missense | HECW1 | GRCh38.p7 | 7:43444383 | GCAGTGTCCCCGATG[A/G]TCCAGGGAACCAAAG | 23072 |
rs370382137 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132644 | AATCAGTATTCTTCA[C/T]GGTGCTCAAATTAAC | 23072 |
rs370399215 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43358132 | CCTTTCCACCCAACT[C/G]AGATGAAGGTGAGGC | 23072 |
rs370402119 | snp | A/C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488202 | GTAATCCCAACTACT[A/C/T]GGGAGGCTAAGGCAT | 23072 |
rs370406437 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43327177 | GTTAAGTCTACATGA[A/G]GAGACTGAACCCCAC | 23072 |
rs370407166 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43171301 | GAAACACAGGCACAT[-/AC]ACACACACACACTCA | 23072 |
rs370420253 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43318390 | CCAAACAGGGCTGTG[A/G]GCACACACTGTGAAT | 23072 |
rs370424283 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43450462 | AAAACGCTGCATTTC[C/T]CTCAAACAGGCCTAT | 23072 |
rs370431004 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43257246 | GTCAAGTAAATTTGG[A/G]AAACACCAAGTTAAA | 23072 |
rs370431547 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43310176 | GTGCTCTTGCAGCAG[C/G]CTTTCTGTTTGGGGA | 23072 |
rs370443067 | in-del | -/TTCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335797 | TTCTTCCTTCCTTCC[-/TTCC]ATCTCTTTCCTTTTC | 23072 |
rs370447926 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481403 | GATAAAGTAGCTGAG[A/T]ACTGCAGACAGATTC | 23072 |
rs370448181 | snp | A/G | 3.45036e-05 | 0.00415338 | missense | HECW1 | GRCh38.p7 | 7:43445190 | ACAGTTGCGAGGGCT[A/G]TGACGCGTCCTGCTG | 23072 |
rs370450979 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43346250 | CCTGATAATTAGTGA[A/T]GTTGAGTATTTTTTC | 23072 |
rs370469956 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43329526 | TAGGAGGTAAGATCA[A/G]CATGGCTTGGTGAGG | 23072 |
rs370472179 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43172921 | GCTAGACCATTTCAC[A/G]TTCGTTTGCCTTTGT | 23072 |
rs370475901 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43228269 | GGCAGGGGAATCACT[G/T]GAGTCTAGGAGTTCA | 23072 |
rs370478859 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250845 | TGAAAAAAATCAAAA[G/T]CTCCTACAGTCCTGG | 23072 |
rs370481097 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43295187 | TGTGAGCAGAGGGAC[A/G]ACTTTGAGTTCTGCC | 23072 |
rs370492415 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226558 | CTGACAGGTCGAAAA[C/T]GACAGTAAAGCAGCC | 23072 |
rs370495692 | in-del | -/GTT | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268772 | GTTGTTGTTGTTGTT[-/GTT]TGTTTGTTTGTTTTT | 23072 |
rs370496625 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43191576 | CCATTTTCTATTTTT[A/G]GCCTTTCAGGTTTCT | 23072 |
rs370510917 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43332689 | CATCCCTGGGGAACA[A/G]TACATGGGCTGCAAG | 23072 |
rs370511112 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43314954 | CACACAGCTGCCTCC[C/T]CTGGCTCAGGACTCA | 23072 |
rs370512238 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120488 | ACCTATTTGTTTACC[C/T]AGTGCCTGGAAAAGT | 23072 |
rs370521844 | snp | A/C/G | 0.00109344 | 0.0233613 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43508078 | GGTGATGGCCTATTC[A/C/G]CGGAAAGAGCTCCAG | 23072 |
rs370525350 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43420331 | AGGACTTAATATATT[A/G]ATAATAATAACAATA | 23072 |
rs370526731 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43528014 | GAGCTATTAGCTAAC[A/G]TTAATAGCTAAACTG | 23072 |
rs370530312 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184567 | AGCTTCAGGATAGGG[A/G]CTGGTCATAAGAAAG | 23072 |
rs370530954 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363834 | ACCCTTCTGGTTAAG[C/T]GATCATTTGGCTATA | 23072 |
rs370531251 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43460093 | TTGTCACTGTTTTTT[C/G]TCACAAGGGCCTGCT | 23072 |
rs370537062 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43232276 | CCTCCACTGGTGAAC[C/T]ATAAGAACCCTCCTT | 23072 |
rs370540376 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43477467 | TTGTGTGTTTAAAAA[A/G]CATGTTGATGCATTT | 23072 |
rs370542628 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43311900 | CATGGACCTCAGGGG[C/T]GGCCCCCACGATGGC | 23072 |
rs370544005 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43479229 | TGATTAGATGCTGCC[A/G]TCTGGGGGTAACGAG | 23072 |
rs370546957 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43321123 | ACCCTCCAGTTTTGC[C/T]TTTGCTTGACCAAAT | 23072 |
rs370563396 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523640 | GGGAAACGCCATCTC[A/G]AAAAAAAGAAAAGAG | 23072 |
rs370563502 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138441 | TAATTAGGAACCACC[A/G]GGTGGTTTTCTTCTG | 23072 |
rs370567174 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43353178 | ATATATTATTGATGC[A/G]TGTGTTTTAATATTT | 23072 |
rs370572941 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224071 | TTAGTTTTATTCGTT[A/G]CCTGTCTTCTCACTC | 23072 |
rs370598048 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139711 | ATTTTATATTGTTCC[C/T]GGCTTCTAATCTTTT | 23072 |
rs370603869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124938 | AAAACTGTGTTTTCA[A/G]GATGCCTTAGTTTGG | 23072 |
rs370635970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43341005 | TGAGTTCATGTCCTT[C/T]GCAGGGACTTGGATG | 23072 |
rs370654998 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132233 | GTCTATATATTATAG[A/T]TGTTAACTATCATTT | 23072 |
rs370655637 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43501759 | TTCCTTGAGCCCAGC[A/G]GGTTGAGGCTGCAGT | 23072 |
rs370658021 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43188829 | TTGGCCAACAGTACA[C/G]TGCCTTCTGCTAACA | 23072 |
rs370666485 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160888 | CTGTGCCTTTTACAG[A/T]TGTCGTATTTATTTA | 23072 |
rs370683166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123273 | GAGCTACTCACAGTT[C/T]GGTCATTAAACAGAA | 23072 |
rs370684453 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43482344 | AAATAGAGGGGAGTG[A/G]GTGGTAGGAAATGTT | 23072 |
rs370685226 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43536709 | CAACACAGCCTGAGG[A/G]GTAGAGGTGAACATG | 23072 |
rs370695300 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43370934 | GCTCTGTCACCCAGG[C/G]TGGAGTGCAGTGGCG | 23072 |
rs370705974 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43265186 | TCTGCTCATTCTAGC[C/T]GCTCTTGGTCCTGGT | 23072 |
rs370706641 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166530 | CTGAGCCAACTCTTA[C/T]TATTACTGATATTTT | 23072 |
rs370708913 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151965 | TCTAATTTCATGAGT[A/G]AAGACATAAATTCTA | 23072 |
rs370711857 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | HECW1 | GRCh38.p7 | 7:43500640 | GAGATCAGAAGAAAA[C/T]GTATTTCTGAGTTTA | 23072 |
rs370719751 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269994 | TTTCTCAGCCTCTAT[A/G]TCTTCATCTCTGAAA | 23072 |
rs370721022 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43387265 | CGAGGTTATGGAAAC[A/G/T]GATTCATCTTCACTC | 23072 |
rs370723015 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416450 | TGTCAGACAGGGACA[C/T]TTAAGTCTGCAGAGG | 23072 |
rs370723063 | snp | A/G | | | missense | HECW1 | GRCh38.p7 | 7:43463733 | CAAAGCTGCGAGCAA[A/G]CCCCAGCAGGAGGAG | 23072 |
rs370726762 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43392824 | CCTGTCAACTGAGCT[A/G]TAGTCTCCGGACTGC | 23072 |
rs370728439 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43289981 | GAAAGCTTGAGTTAG[G/T]ATAAAGCGGGTTGTG | 23072 |
rs370731457 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43246561 | CCTGGTTGAGAAACA[C/G]TAGCTAGACCTGACG | 23072 |
rs370734704 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268559 | CCACTGTGCCCTGGA[C/T]AGCCTCACAGCAAAG | 23072 |
rs370737414 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481001 | TGATAAAATGAATGT[C/T]TTTTCATGGAGTCGT | 23072 |
rs370739489 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43499274 | AGCAACAGAGTGAGA[A/C]CCTGTCTCAAAAAAA | 23072 |
rs370740209 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281552 | AAACACAAGCTCTTT[C/T]AAGTCTGTAGCCTCC | 23072 |
rs370769054 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361800 | TCATGCTAGTGGAAA[A/T]AAAAAAGACTCTCTC | 23072 |
rs370769327 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43148995 | ACAGAAGAATTCCAA[C/T]TGATAAACATAGAAG | 23072 |
rs370783862 | snp | A/G | 3.31246e-05 | 0.00406955 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43466517 | GCTGCAGTCCCCAGC[A/G]GTCAAGTTCATCACC | 23072 |
rs370802380 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111414 | AAGGTTTGAAAATGG[A/T]CTGCTTTGAGCTCAT | 23072 |
rs370816242 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210939 | AAGATTTAATAGAGT[A/G]AAAACAGAGCTCCCA | 23072 |
rs370823441 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43174886 | CAACTCAGATGGAAT[A/G]TACTTACTCATCTCT | 23072 |
rs370825288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43373451 | GCATGAGCCACCATG[C/G]CCGGCTCCTTTCTTT | 23072 |
rs370827560 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43441523 | CTGCACAGGAAAAGC[A/G]GGCCAAGGACATCCG | 23072 |
rs370836410 | in-del | -/T | 0.192088 | 0.2432 | intron-variant | HECW1 | GRCh38.p7 | 7:43529957 | TTTTATTTTTATTTA[-/T]TTTTTTTTTTGAGAC | 23072 |
rs370838701 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43239347 | ACTTTGTCTTTGCAA[A/G]GGTGTCTAGTGTGAC | 23072 |
rs370839722 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43241225 | GGCTGCGAGCAGGGA[G/T]TAGAAGCACTCATCA | 23072 |
rs370841701 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422915 | CACCTGGAGATAAAT[C/T]GCAGTGCCTGGCCGA | 23072 |
rs370846695 | snp | C/T | 1.65625e-05 | 0.00287766 | stop-gained | HECW1 | GRCh38.p7 | 7:43312015 | TCCATCGGGCACTCT[C/T]AGGACCTGGTCATCC | 23072 |
rs370847544 | snp | A/G/T | 0.00358923 | 0.042236 | intron-variant | HECW1 | GRCh38.p7 | 7:43360758 | ATGAGGAGCATCATT[A/G/T]TCGAGTGTGGCCTGG | 23072 |
rs370853992 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43334677 | GGAGAAAGTCATCCT[C/T]GTTTTATTGTCATTA | 23072 |
rs370855131 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488501 | AGAGAAAGAAAGAAA[-/A]GAAAAGAAAAGAAAG | 23072 |
rs370861953 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43319756 | AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 23072 |
rs370863268 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198278 | ACACACACCCCACAC[-/TC]ACACACCACACACAT | 23072 |
rs370869877 | in-del | -/CTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43393677 | CTCTTTTTTCTTCTT[-/CTT]TTTTTTTTTTCATCT | 23072 |
rs370876449 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43211754 | GGATATTGAACAAAG[A/G]GAAAACCTTTCTCAA | 23072 |
rs370880175 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179085 | GAAAGCATTTTCTCC[A/G]GAATAATTCATCTCC | 23072 |
rs370894030 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43261809 | TGAGTGCTTCTGTCT[C/T]ATAACAAAAGAGTAA | 23072 |
rs370898406 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43235310 | CCCTCCTTGATGGGG[-/G]ACCTCTGTCCTCCCA | 23072 |
rs370900800 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43265818 | CAACTACAAATTTGA[A/G]GGTTCCCAAAACTCC | 23072 |
rs370909719 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43321391 | TGGCAGGCTTTTTTC[A/G]TGGGTCCCCATACTG | 23072 |
rs370918834 | snp | A/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299682 | TAAGTGTCGCCTGAG[A/T]CGTTTAAGAAATCAT | 23072 |
rs370928206 | in-del | -/ATAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43341308 | AGAACTTACAGTATT[-/ATAA]ATAAATAAATAAATA | 23072 |
rs370943885 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43496013 | TAATTCCCTACATAA[A/G]TGAGTGGAATGTATT | 23072 |
rs370946514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43404944 | TTACACCATTGCACT[C/T]CAGCCTGGGCAACAA | 23072 |
rs370958178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328459 | TGCGGTTGCTGCTGG[C/T]CCCTGTCTGAACTGC | 23072 |
rs370964458 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289509 | TGTTCTTACTTGTCT[A/G]AATGATAGCTTGGAC | 23072 |
rs370974815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136200 | GCGCCTGATACTACT[A/G]TAGACAGGATGAGGG | 23072 |
rs370978522 | in-del | -/CT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335865 | TCCCTTCATCTCTCT[-/CT]TTCTCTTTCTCCCTT | 23072 |
rs370986258 | multinucleotide-polymorphism | CTG/TTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190084 | TCACAGCTGTGGAAA[CTG/TTT]TTGTTGTTGTTGTTG | 23072 |
rs370997480 | snp | A/G | 1.69789e-05 | 0.00291362 | missense | HECW1 | GRCh38.p7 | 7:43554708 | TCCAGCGTGCCCTAC[A/G]AAGGCTTCGCAGCCC | 23072 |
rs370998170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163117 | AGCACACAGCACAGA[C/T]GAGAACAGTCCCAAA | 23072 |
rs371023435 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487109 | AGAGGAATGTAAATT[C/T]GTCCTTTGAGCCCTT | 23072 |
rs371035408 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43502942 | TTGGTAATAAGCTTT[A/G]TCTCTGAGAAGGGAT | 23072 |
rs371036156 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287513 | TCTTTTCATTTTCTT[A/C]TTTGTTTGGAGACAG | 23072 |
rs371038225 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43169471 | CCCCTGGGAGATACA[A/C]CCTTTTCCCCATTGA | 23072 |
rs371039151 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517621 | ATTATGAGATCCCAC[C/T]GGGTGTCTCATGGCC | 23072 |
rs371047353 | in-del | -/A | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118241 | GAAAGAAAAAAAAAA[-/A]GATCAAAATTCACAT | 23072 |
rs371051063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154753 | AGACATCTCCCTGCT[C/G]TCAAACCTTCCTTCA | 23072 |
rs371052236 | in-del | -/CCTCCCACCTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43459103 | CCTGCCTCCCACCTG[-/CCTCCCACCTG]AAACATATCTCATCC | 23072 |
rs371063111 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187504 | ATAGTTCATTATATT[A/G]TCTATATTTTATTCT | 23072 |
rs371068408 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264838 | GACAGAGTGAGACTC[A/G]GTTTAAAAAAAAAAA | 23072 |
rs371070618 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43436495 | TATGGGTGGGGCTGT[A/T]TTACAGGATTTGGGT | 23072 |
rs371070745 | snp | C/G | 3.33923e-05 | 0.00408596 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508952 | ATGAGCTTCCTGGAC[C/G]TCTGCTTTCTTTGCA | 23072 |
rs371074024 | in-del | -/T | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510061 | ATGAGGTAGAGTGAG[-/T]GAGTACACATCGAGG | 23072 |
rs371076462 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43367714 | TTTACAAGATCTTCT[A/G]ACTATTGTTAACTTT | 23072 |
rs371078204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213662 | GTGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC | 23072 |
rs371083129 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43175165 | TTTGATGTACAACAC[A/G]ATGTGTGTGTACACA | 23072 |
rs371093893 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225298 | AAAATAGGTGAACTG[C/T]ACAGATGGTGGGAGA | 23072 |
rs371096092 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43391658 | CCCCTAAAGTTGGCT[C/T]TGCCCTTTCAGTTTA | 23072 |
rs371096961 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300072 | TTGCCTCGTTGTGAT[C/T]TCTTTCTTCTATCAA | 23072 |
rs371097723 | in-del | -/TTTA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412425 | ATGCTTTTCATTTCT[-/TTTA]TTTATTTATTTATTT | 23072 |
rs371098297 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350167 | GCTGATAATTGTTTT[G/T]TTTGAGGAGGCTGAA | 23072 |
rs371101030 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145983 | CCACAGTTAAATCAC[A/T]CCTGGATTTATCACT | 23072 |
rs371107271 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43221595 | GGGACAGCCTGTTGC[C/T]CAGGCTGGAGTGCAG | 23072 |
rs371107840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43337274 | GTGATTTTAATTTGC[A/T]TTTCTCTGATGATTA | 23072 |
rs371125301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43548500 | GAAGATTGAATTGCA[A/G]CCCTTCTTTTGTCAA | 23072 |
rs371126806 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468456 | GTCCCAAGCTGCACA[C/G]CACTCAGGTGGAACG | 23072 |
rs371138407 | in-del | -/AGGA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247744 | GAAAGGAAGGAAGGA[-/AGGA]GGGAGGGAGGAAGGG | 23072 |
rs371180560 | snp | A/G | 1.66078e-05 | 0.00288161 | missense | HECW1 | GRCh38.p7 | 7:43407703 | CCAAGATCATAGGCA[A/G]CACCGTGAACCCCAT | 23072 |
rs371183033 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43452999 | GGTGATGTGGTTAGC[A/G]AACTAGCAAGGCCCA | 23072 |
rs371188788 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43163732 | CCTAATCTTGTTCAT[A/T]CCCTCCTTGCCTGCT | 23072 |
rs371190628 | snp | C/T | 2.15775e-05 | 0.00328455 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445032 | GGACAGAGAAGAGCC[C/T]GAGGGGGCTACTCCA | 23072 |
rs371194669 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293213 | CGACACAGCGAGACT[A/G]TGTCTCAAAAAAAAA | 23072 |
rs371208054 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43286698 | CAAAGGTGTTTGGGA[A/G]GAGGGATATCACCAA | 23072 |
rs371217218 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43285207 | CAGGTTGTTGTGAGA[A/G]CTTCCTGGGATTAGA | 23072 |
rs371217377 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514713 | TTTCTATCTTTAGGG[A/G]TACATAATTTAATAA | 23072 |
rs371222025 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237301 | ATAAAATGTAAATCA[C/T]TGGAGAAGACCTGCC | 23072 |
rs371228210 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43252953 | GGGAGTCCAGTGGCC[A/C]ACCTTGGTTAGAGTT | 23072 |
rs371230534 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43262806 | TGGGCCACTATCCTT[A/G]TCCATTTGCACTTCC | 23072 |
rs371234373 | snp | A/G | | | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43249291 | CCCAGTAACTGTTCC[A/G]GAGCGTCAGCCTGAC | 23072 |
rs371235018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43241814 | ATACATAAACAGTTC[A/T]TTAGAATTATTTTTA | 23072 |
rs371237942 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43385165 | ATCGGTCACCAAGTT[A/C]TATCCATTTTATCAC | 23072 |
rs371238353 | snp | A/C | 1.6563e-05 | 0.00287771 | intron-variant, missense | HECW1 | GRCh38.p7 | 7:43450884 | CTTCCTTCCCTGAGG[A/C]CTGAACATCATCACT | 23072 |
rs371243016 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412953 | GCATGATTTATACTC[A/C]TTTGGGTATATACCC | 23072 |
rs371244959 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43191424 | AACACATGCAGAGCC[A/G]GAATGGGGACATGCG | 23072 |
rs371245834 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43397029 | CTGTAAAGCAAAAAT[G/T]TTTTTTAAATCTGTT | 23072 |
rs371250675 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487488 | CATGTCTGGGGAAAG[G/T]CAGGCCACCAAGGGC | 23072 |
rs371252875 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43207453 | GCCATCTCAAACATT[C/T]ATCATTTCTTTGTCT | 23072 |
rs371256559 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43221615 | CTGGAGTGCAGTGGC[A/G]CTATCTCGGCTTACT | 23072 |
rs371282236 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134723 | TCAATATTTGGGGGA[A/T]TTTTTTTTCTTACTT | 23072 |
rs371287345 | in-del | -/TCAGGCTTCTCAACAAGCCTGAGGCTCC | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302207 | ACAGCCTGAGGCTCC[-/TCAGGCTTCTCAACAAGCCTGAGGCTCC]CTCCCAAGCCAGGCA | 23072 |
rs371289616 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166839 | TGGGGCCAGGGAGGG[C/T]AGCACAGGCCCAGGC | 23072 |
rs371289731 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43551088 | TGTCCTTGAACTCCA[G/T]TTTAAAAACCAGAGG | 23072 |
rs371294152 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43532778 | TTCCCCAAAAGAAAC[A/C]TGGAGCCCAAATTAT | 23072 |
rs371313868 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413280 | TCTGTTCATGTCCTT[C/T]GCCCACTTTTTGATG | 23072 |
rs371319359 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43401142 | GGCTCCAAGGATTAG[G/T]ATGTGAACATCTTTG | 23072 |
rs371332417 | in-del | -/CA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43340693 | CCTAAATTAAAGCTA[-/CA]GTGTCGTCTGTTGGT | 23072 |
rs371345945 | snp | C/G | 0.000167986 | 0.00916322 | missense | HECW1 | GRCh38.p7 | 7:43492100 | TTTCTAGAAACAGAG[C/G]AGCCTCTTTACTGGC | 23072 |
rs371345997 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43317879 | GTCATCCTTTGCTGA[G/T]TCTTCCCACCTCCCC | 23072 |
rs371348651 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43411131 | CAATTATTTAAGCAA[A/T]AAGTTTTCTTCTAAT | 23072 |
rs371357329 | snp | A/G | 0.000132668 | 0.00814348 | intron-variant | HECW1 | GRCh38.p7 | 7:43552213 | GCTGAAGCCTAACCT[A/G]CATTTCAGGTTGTAG | 23072 |
rs371359658 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43276788 | TCCTGAGGAGCAAGT[C/T]CTTTATTTGGCACAT | 23072 |
rs371361987 | snp | A/T | 1.65919e-05 | 0.00288022 | missense | HECW1 | GRCh38.p7 | 7:43438009 | TCATTGCAGCAATTC[A/T]GTTTTGTGTCCTTGC | 23072 |
rs371363667 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43434369 | TTGGTCTAACATGGC[A/G]TGGGCCTTCTTTTCC | 23072 |
rs371364716 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43425135 | AGCCATAAAGCCATA[A/G]CAATGGAGTTGCAAC | 23072 |
rs371365551 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350962 | TATCATATTACCAGG[G/T]TTGGTGTTTTCTGGT | 23072 |
rs371366052 | snp | A/G | 0.450483 | 0.149354 | intron-variant | HECW1 | GRCh38.p7 | 7:43416614 | tgggcaatggcgggc[A/G]cccctcccccagcct | 23072 |
rs371372437 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43545250 | ATTTTATGGCCTTCT[A/T]CACCACTTGAATTTT | 23072 |
rs371372725 | snp | G/T | 8.33688e-05 | 0.00645581 | missense | HECW1 | GRCh38.p7 | 7:43492173 | TCAACATGAGTCATT[G/T]CCACTGGGTATGTAT | 23072 |
rs371375824 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43397027 | ATCTGTAAAGCAAAA[A/C]TGTTTTTTAAATCTG | 23072 |
rs371382026 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43474253 | AGCAGATCGAGACCA[C/T]CCTAGCTAACATGGT | 23072 |
rs371394904 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43534504 | ACATCTTTCCATACA[C/T]TGACTCAGCCCCTAA | 23072 |
rs371422517 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43337830 | TTTTTTTTATAGAAG[A/G]CACTCACTTGCTGTG | 23072 |
rs371434353 | in-del | -/T | 0.474091 | 0.11083 | intron-variant | HECW1 | GRCh38.p7 | 7:43381489 | ACCATGCATGGCTAA[-/T]TTTTTTTTTTTTTTT | 23072 |
rs371439876 | snp | C/T | 4.97211e-05 | 0.00498579 | missense | HECW1 | GRCh38.p7 | 7:43438106 | TCTTGGGAAAGCTGT[C/T]GATGCCCGTTCAAAG | 23072 |
rs371441177 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43211041 | TATTGTCCCTCCTGC[A/T]GTGCTCTCAGGCGAT | 23072 |
rs371450163 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225331 | CAACTCTTCCCTTCC[C/T]TTTGGTGAGCACGAA | 23072 |
rs371451264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43334093 | GCCAAGTCAATGGTT[A/G]TGCATAGCCACAGCT | 23072 |
rs371468261 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43240138 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 23072 |
rs371472883 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43216891 | AACCCCTGGCCTCAA[C/G]TGATCCTCCCATCTC | 23072 |
rs371473478 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43257850 | TGCAATTAGAAATAA[G/T]AAGAAGAATAGTGGT | 23072 |
rs371485400 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43549098 | GTTCAGTGCAGCCGG[A/G]CAAAGGAACACACAG | 23072 |
rs371488146 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156286 | TCTCTGAGGTATCTG[A/G]GACAGAGCAGGCCCC | 23072 |
rs371489488 | snp | C/G/T | | | intron-variant, upstream-variant-2KB, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113672 | CTGCCGGGGCGGGGA[C/G/T]GGGGGGGGAATGCGT | 23072 |
rs371490477 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43530052 | CCTCCCAGGTTCAAG[C/T]GATTCTCCCACCTCA | 23072 |
rs371491837 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215480 | TGTCTTTCATTTCTG[A/T]GCAGTATGTAATTGC | 23072 |
rs371497592 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143359 | CTTGATCACAGCTAA[C/G]TGCAGCCTCAACTTC | 23072 |
rs371498514 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43503676 | CGTTGATTTTAAACT[A/T]TACAATCCCCATTCT | 23072 |
rs371501130 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180876 | TCTCTTGTAACTATT[A/T]TGAAATATGCAATAC | 23072 |
rs371501613 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184798 | GCTGTTCAGGAAACA[C/G/T]GATGCTGGCATCTGC | 23072 |
rs371504021 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43200785 | CCTCCCTGTTGGATA[A/G]TAAGTCTTATTATCA | 23072 |
rs371511975 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130610 | GCATATCATTAATAT[A/T]GTGATAAACAATGTG | 23072 |
rs371514122 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160555 | TCCATTCTCCCTTGG[C/T]TTGGAAATGTCACTT | 23072 |
rs371514188 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43559839 | TGTTCGTTCATTCTA[A/G]ATGACAAACTAAGGG | 23072 |
rs371517177 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120646 | TCTATTTATTTATTT[A/G]TTTGTTTTATTTTTT | 23072 |
rs371519099 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43236160 | AACACTAAAACTTCA[C/T]GTGTGGGCATATGAA | 23072 |
rs371526844 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43186189 | TTCTCTGATTCATTT[A/C]TAACCCCTACATGAT | 23072 |
rs371529063 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130092 | AAATACAATTTTTTT[-/T]AAGCTTTGACTTACA | 23072 |
rs371530320 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454135 | AGCTTTTTCCCTTAA[C/T]TTATAAAAGCCAACC | 23072 |
rs371543059 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43272077 | TCTCCAACAAAATTG[A/G]CAAAAATAAACAATA | 23072 |
rs371546687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43558038 | AAGAATGTCCATCCA[C/T]GTCACAGCGTGTGGG | 23072 |
rs371546945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43287105 | GGAATGTACCTTGTT[G/T]TGAGAGGAAATGAAC | 23072 |
rs371553240 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184881 | GGCAGGTCTTACATG[-/G]CTGGAGCAAGAGGAA | 23072 |
rs371557446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43200154 | TCAAACGGATTTGAT[C/T]GGCCCAAATTAGAGT | 23072 |
rs371559613 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43266440 | TCCCGGGTTCAAGCA[A/G]TTCTCTGCCTCAGCC | 23072 |
rs371561046 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43388748 | ATGCCTCAGCCCCTC[C/G]AGTAGCTGGGATTAC | 23072 |
rs371562612 | in-del | -/AGAGAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487965 | CTCAAAAAAAAAGGA[-/AGAGAG]AGAGAGAGAGAGAAA | 23072 |
rs371569992 | in-del | -/GTAGGTAGGTAGGTAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237141 | GAAGGAAGGAAGGAA[-/GTAGGTAGGTAGGTAG]GTAGGTAGGTAGGTA | 23072 |
rs371570213 | snp | A/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358651 | ATAATCAAATAAATG[A/T]AACAAAAATAATAAT | 23072 |
rs371572204 | in-del | -/AACA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376114 | TAACCCAATAAACCA[-/AACA]TATACTCACCTATTA | 23072 |
rs371576828 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43193607 | GGCTGGTCTTGAACT[C/T]CTGACCTCAAGTGAT | 23072 |
rs371577216 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43327658 | TAAAATCCCAAAAGA[A/G]TTAATCTTGCTAGAG | 23072 |
rs371602884 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297080 | GAATCTCCAGGAAGA[A/G]GGCTGTTTTATTTTT | 23072 |
rs371604134 | snp | C/G | 3.34057e-05 | 0.00408678 | missense | HECW1 | GRCh38.p7 | 7:43493176 | GCAAGAAACCACACA[C/G]TCAGGTAAGCCTCGC | 23072 |
rs371604411 | snp | C/T | 1.76024e-05 | 0.00296663 | intron-variant | HECW1 | GRCh38.p7 | 7:43320598 | TGCTGTTGACTGATA[C/T]GTTTCTCTGCTCTGC | 23072 |
rs371606271 | snp | C/T | 3.31318e-05 | 0.00406999 | synonymous-codon, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509086 | CACGGTGCAGATCAG[C/T]CCCATGTCCGCATTT | 23072 |
rs371608534 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140657 | GTGCTCAGTATTCTC[C/T]CACGAGATTAGGAGA | 23072 |
rs371612774 | snp | A/G | 1.65825e-05 | 0.00287941 | missense | HECW1 | GRCh38.p7 | 7:43561867 | TATCCCTCGTACTCC[A/G]TGTTGTATGAAAAGC | 23072 |
rs371614099 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328543 | GTGGCAGTGGAGGGC[C/T]CAGCCCACGTGGGAA | 23072 |
rs371624110 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43559413 | GCCACAAGTATGACA[C/T]GGTTCCCCAAATCAT | 23072 |
rs371624684 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143477 | TTTTGTTAGAGACAG[A/G]CTCTCACCATGCTAC | 23072 |
rs371626508 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529180 | TCATTCTACAGCCGG[C/T]GTTCCCACCTCCTCC | 23072 |
rs371631503 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287469 | AGTCATGGAAGGTTT[A/G]GCAGAGGGGATGTGA | 23072 |
rs371633447 | snp | C/T | 1.65831e-05 | 0.00287945 | missense | HECW1 | GRCh38.p7 | 7:43501265 | CAGGCTGCCTTCCAC[C/T]CTGGGTATAGCTTCT | 23072 |
rs371637082 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43402069 | TCTTCCCACTCCATC[C/T]TCTTTCCAGCTCACC | 23072 |
rs371643109 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43386827 | GAAGCTCACCGCACT[A/G]TGCTTTTATTTTTTA | 23072 |
rs371649837 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43530438 | AAAATTTAATATACA[G/T]AAGAAAATATCTCCA | 23072 |
rs371652643 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | HECW1 | GRCh38.p7 | 7:43552246 | TCGAGGCTGGTGTCC[A/G]TGTTTGATGCCAGGG | 23072 |
rs371655287 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant | HECW1 | GRCh38.p7 | 7:43243943 | TGAAGGTCAGTGTGC[C/T]TTTCTGATTATAAGA | 23072 |
rs371663336 | snp | C/G | 8.39581e-05 | 0.00647858 | missense | HECW1 | GRCh38.p7 | 7:43445293 | CTACAGCCCCTCCTG[C/G]TACAACGGCAACAGG | 23072 |
rs371669920 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43393191 | CAGAGAGAGGGGGGG[-/G]CAACAGGACCCAGCA | 23072 |
rs371685011 | snp | C/T | 3.34902e-05 | 0.00409194 | intron-variant | HECW1 | GRCh38.p7 | 7:43466595 | AAAATGCAGAGGGGG[C/T]GGCCTGGCTCGGCAA | 23072 |
rs371710535 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429313 | ATATATATATATATA[C/T]ATATATATATATATA | 23072 |
rs371714515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43383886 | CATATTCTTACAATA[A/C]AGTAAGCTAGAGAAA | 23072 |
rs371715882 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413210 | TGATGGCCAGTGATG[A/G]TGAGCATTTTTTCAT | 23072 |
rs371718294 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129918 | TGTAAATAGGGGTTA[C/T]ATTGTTTAGGGAGTA | 23072 |
rs371747745 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297811 | GCATGGTGGCTCACG[C/G]CTATACTCCCAGCAC | 23072 |
rs371756066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43194339 | ATGCTGAACTAAAGT[G/T]AGATTTTCTCTTCCT | 23072 |
rs371757389 | in-del | -/TTTTTAGTA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141673 | CCGGCTAATGTTGTA[-/TTTTTAGTA]GAGACAGGGTTTCTC | 23072 |
rs371767240 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166452 | AAGCTATAATAGTAT[C/T]AGGATCTAGAAGCAG | 23072 |
rs371770049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43334776 | CTTAGAGGGGAGAAA[C/T]TGTGACATTATGCTT | 23072 |
rs371777129 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336250 | GATCATACCTCACTG[C/T]GGCCTCAAGGGCTCA | 23072 |
rs371781370 | snp | A/G | 1.74522e-05 | 0.00295394 | missense | HECW1 | GRCh38.p7 | 7:43444448 | GTCATCACGGAGGCA[A/G]GAGACCAGGGCATGG | 23072 |
rs371782002 | in-del | -/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516775 | GGAATTACACAAACC[-/T]AGATGGCAGAGCCTA | 23072 |
rs371786281 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343587 | CATGTCCCTGCAAAG[A/G]ACATGAACTCATCCT | 23072 |
rs371795853 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359083 | CACCCACCTCGGCCT[C/T]CCAAAGTGTTGGGAT | 23072 |
rs371797444 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43262440 | ATGAAACTGAGGCTG[A/C]AGGGATAAGTCCTGG | 23072 |
rs371798038 | in-del | -/TATT | 0.485664 | 0.0834419 | intron-variant | HECW1 | GRCh38.p7 | 7:43308246 | TAATAATATATAATA[-/TATT]TATATATATTATATG | 23072 |
rs371806516 | snp | C/T | | | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444600 | GCTGCTGGAAGACGG[C/T]GAAGCCCCAGCCAGC | 23072 |
rs371807557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43361039 | TTTCTTCACTTTCCT[A/G]TTTTGTTCTTGTGCG | 23072 |
rs371811045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43422525 | ACATCACTACGCCTG[G/T]TTAATTTTTTTGTAT | 23072 |
rs371812687 | in-del | -/ACAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43345826 | CACACACACACACAC[-/ACAT]CATATATATATACAC | 23072 |
rs371837143 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43256656 | AACATCAAAGTAATT[C/T]CTGATTAATAATATC | 23072 |
rs371865052 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43338084 | ATTATTCTCTCCACT[-/T]AGATTGAAACACAGA | 23072 |
rs371882813 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43312184 | TAAAATATACAAGCA[A/C]CTGTGTTATATGCCA | 23072 |
rs371885142 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43292671 | AAGGTGACCTTTGGT[C/G]ACATACCTCTTCCAT | 23072 |
rs371891485 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112796 | ACCCGGCAGCCAGAG[A/C]GCAGCGAGAGCGGGC | 23072 |
rs371902700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43535985 | GAAAATAACTTATAT[C/G]AGAGTCCAGGAATGT | 23072 |
rs371914325 | snp | G/T | 0.000625804 | 0.017678 | missense | HECW1 | GRCh38.p7 | 7:43445225 | CCCTCGTGCTACAGC[G/T]CCTCGTGCTACAGCA | 23072 |
rs371924735 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43502960 | TCTGAGAAGGGATGT[C/T]GCACTCAGAGTTAGT | 23072 |
rs371928003 | snp | A/C/T | 0.000431499 | 0.0146821 | intron-variant | HECW1 | GRCh38.p7 | 7:43479763 | ACCCTCCCTACACCC[A/C/T]GCCCTACTGTTCACC | 23072 |
rs371932543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43281857 | ATGGGTGTGAGCCAC[C/T]ATGCTTAGCTCAGAA | 23072 |
rs371936990 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43233972 | ATAAGATACTTCATA[C/T]CATCCAGAAATAAGC | 23072 |
rs371948423 | snp | C/G/T | 0.000704578 | 0.0187569 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444549 | TGCAGAAGAGCTGGC[C/G/T]GAGCAGCTGGACCTG | 23072 |
rs371964101 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308261 | ATATATATATTATAT[A/G]ATATATTTATATATT | 23072 |
rs371967068 | snp | C/G | 1.75382e-05 | 0.00296121 | intron-variant | HECW1 | GRCh38.p7 | 7:43468877 | TGCTCTATGTTTTTC[C/G]TAATTCCCCACTCCT | 23072 |
rs371968890 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43347131 | ATCCATGAGCTTGGG[A/G]TGTGTTTCCATTTGT | 23072 |
rs371969375 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348490 | ATTTATCTTTTGTAA[-/T]TTTTTTTTTTGTTTC | 23072 |
rs371972218 | snp | C/T | 0.000102661 | 0.00716378 | intron-variant | HECW1 | GRCh38.p7 | 7:43463621 | CCCCCAAGGAGCAAA[C/T]CAAAGTTAACTCCTG | 23072 |
rs371975020 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307919 | ATATATATATATATA[C/T]ACACACACATATAGT | 23072 |
rs371976019 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316522 | TGAGGTAGGTACTTA[C/T]AGTATTTATCCTCAT | 23072 |
rs371980373 | in-del | -/G | 0.0478132 | 0.147039 | intron-variant | HECW1 | GRCh38.p7 | 7:43265950 | GAAGAGGAAACTTGA[-/G]GGGGGGGTGTGGATT | 23072 |
rs371997052 | snp | C/T | 7.06277e-05 | 0.00594213 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43550516 | CAAGAAGGAGTACAT[C/T]GAGCGCATGGTGAAG | 23072 |
rs371997928 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242488 | AGGAACCATGACTAA[A/G]GCTAGACTTTTAAGG | 23072 |
rs372002680 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242373 | ACCGTTAGGAGGTAG[A/G]AGCAGACGAACTCAG | 23072 |
rs372005698 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | HECW1 | GRCh38.p7 | 7:43479689 | ACGGTCGTCTTCCCA[A/G]TCATCTAACTCACCG | 23072 |
rs372008399 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361810 | GAAATAAAAAAGACT[-/AT]CTCTCTTTTTTTTTT | 23072 |
rs372011835 | snp | C/T | 3.31774e-05 | 0.00407279 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43360917 | CTTCAAATACTACCA[C/T]GGAGTGAGTGGGGCC | 23072 |
rs372012214 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43306762 | AAAACTGACAGAGCA[C/G]AATCTTTTGTCTCCA | 23072 |
rs372024816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154009 | TGTAGCCTTAATCTT[A/G]TTACTCAAATTCCAT | 23072 |
rs372029720 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43201809 | ACGAAAAAAATATAT[C/G]CTTGAAGATTTCATT | 23072 |
rs372029993 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350800 | GATTTCCTTGCATTG[A/G]GCTTCGCCCTTCTGT | 23072 |
rs372031529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43170574 | CCGGAAGGGACAGCA[C/T]ACTCTCACTGGCAGA | 23072 |
rs372033451 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43222066 | GCCATTCATATGGAC[A/G]TTAAGGTTTAAAAGT | 23072 |
rs372035754 | snp | G/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43113086 | CCTCTCGCTTCTCCC[G/T]CGAGGTTCAATTGTC | 23072 |
rs372048028 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43528315 | TGGACACATCTAGAT[-/A]ACGGGAGGAAATCAA | 23072 |
rs372059895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43540499 | AGGAAGTCAATGCTC[C/T]GACAAGCATTTAAAT | 23072 |
rs372065591 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43498026 | GGTCAAGGGATATAT[A/G]TAGGAGAGACAGCTG | 23072 |
rs372072192 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140509 | CCGTGAAGAACCACA[C/T]ATCGAATCCATCGTT | 23072 |
rs372074561 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43175836 | TTCTAGTCACGTTTT[C/G]CTTCTCACAGGCGCA | 23072 |
rs372075253 | snp | A/C | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296521 | GCGGCGCAGCTGTGG[A/C]CGCAGCTGCGGAAGC | 23072 |
rs372089733 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140703 | AATGCTCCCTTTTTG[C/T]GGTATCAGCTCGGCT | 23072 |
rs372099246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207598 | CTAGCTGAAATTTTA[C/T]GTCTTTCAACATACC | 23072 |
rs372102431 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161838 | TGCAAAGTGTCTTCA[A/T]TGTGGTGTCACTTGT | 23072 |
rs372103180 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43430775 | GCCTCCATTTTTATT[A/T]TTCTTTATTATTATT | 23072 |
rs372107609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43371126 | TCTCCTGACCTTGTG[A/T]TCCACCCGCCTCGGC | 23072 |
rs372116387 | snp | C/G | 4.98724e-05 | 0.00499337 | intron-variant | HECW1 | GRCh38.p7 | 7:43552378 | CAATGATCACAAATA[C/G]AACTCAGCACTTTCC | 23072 |
rs372120470 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150339 | TTAGATTTGCTTTAA[C/T]ATTGGAAGGCTACCG | 23072 |
rs372121389 | snp | A/G | 0.000159987 | 0.00894248 | missense | HECW1 | GRCh38.p7 | 7:43469002 | CTCGCAATTTTGAAC[A/G]CTACCAGCACAACCG | 23072 |
rs372141165 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43239030 | GACAATAGATTGGGA[C/T]AAAACAAAATCAGTC | 23072 |
rs372147536 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43386657 | CCAGAAATTCTGCCC[C/T]ACCCACTTCCCCACC | 23072 |
rs372160236 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43561277 | CTTGGAAATGCAGCA[A/C]TTCGACTTTAGGTTC | 23072 |
rs372174722 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43233486 | GAAAAATATGTAATT[A/G]GAAAAGGTGGTGGTG | 23072 |
rs372177905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519358 | TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCTGAG | 23072 |
rs372180931 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43211544 | TCCCAGGGGTGAAAG[A/T]CTTTCCAAGGGGGAC | 23072 |
rs372182089 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43533094 | CTGGCAATGTCAGGA[A/G]GTAGTTTGGGTTGTC | 23072 |
rs372183992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43240159 | CATCCTGGCTGACAC[A/G]GTGAAACCCCATCTC | 23072 |
rs372190958 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43330300 | CTAGCTGTGTTCGGG[A/G]CTGTGTGACAAGAGC | 23072 |
rs372191720 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377105 | CGGACAAGTCAGAGA[C/T]GCCTGGGACTGTGCT | 23072 |
rs372196191 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43165818 | CCTTTCTATTTCTTA[C/T]TTCAATCAGTCATGC | 23072 |
rs372198563 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43479400 | TGGTAATGCTCACTC[A/G]CCCGTGGCTCACCTC | 23072 |
rs372199379 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556952 | GCACCACAAGCCCCC[A/G]AGATGGTTTCTTGGG | 23072 |
rs372208054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43557577 | TCACCCTGTCAGCCA[C/T]GTGGACTTAGTTGCC | 23072 |
rs372217151 | snp | A/C | 0.000155988 | 0.00883004 | missense | HECW1 | GRCh38.p7 | 7:43445285 | GCCTCGTGCTACAGC[A/C]CCTCCTGCTACAACG | 23072 |
rs372224049 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416947 | CTCCCTAGTGAGATG[A/C]ACCCAGTACCTCAGA | 23072 |
rs372230595 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HECW1 | GRCh38.p7 | 7:43469930 | AAGGGAGCTGATGGG[A/G]CATCAATGTCCCCTC | 23072 |
rs372235945 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43525940 | ACTTCTAGGGACTTT[C/G]TCTTTATAGTCTAAT | 23072 |
rs372237419 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43464913 | CTCAAACAGTCCTCC[C/T]AACACAGCCTCCTGA | 23072 |
rs372243561 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43500844 | GCTCTCCTCCATCAC[A/G]GCCACCCTGAAAATG | 23072 |
rs372252522 | snp | A/C | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515532 | AAAACTTGGTGATAG[A/C]TTATAAATGGTGGGA | 23072 |
rs372284507 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43245615 | GCACACAGATCATCA[A/C/T]AGGGGATTTTATTCA | 23072 |
rs372294447 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43355946 | GTGAGCCAAGATTGC[A/G]CCACTGCATTCTAGC | 23072 |
rs372295954 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43320470 | AAGCGTTTGGTCCCA[A/G]TGGCGTCTTGGGGTG | 23072 |
rs372310539 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162076 | CCATAAACAATTGGA[C/T]ATCCACTTTAGTGAA | 23072 |
rs372332330 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133957 | AAGAATTCTTCTCAA[C/G]AGAGAGCTGTACATT | 23072 |
rs372341743 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43222571 | ATCATATTTTCTTCA[A/G]CTGCTACTGCTGAAT | 23072 |
rs372361915 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348955 | TCTTGGAGAAAGTTC[C/T]ATGCACTGTTGAATA | 23072 |
rs372375667 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43553725 | CCCCATAACACCCCC[C/T]GGAAATATTCCTTCC | 23072 |
rs372399788 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416735 | ATAGTCTCGTGGTGC[A/G]CCGTTTTTTAAGCCG | 23072 |
rs372403151 | snp | A/G | 1.67809e-05 | 0.00289658 | intron-variant | HECW1 | GRCh38.p7 | 7:43438171 | GACTGAGATCTTACT[A/G]TCACTAGGTTCCCAC | 23072 |
rs372405076 | in-del | -/TTATTA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315466 | GTCCCATTATTATTG[-/TTATTA]TTATTATTATTATTA | 23072 |
rs372408440 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43425301 | GGTAGATAGATAGAT[-/A]GATGATAGATAGATA | 23072 |
rs372425885 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43493579 | ATAAAAAAGCAAACA[A/G]AAAGTTTCTTGTGTG | 23072 |
rs372431628 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376033 | TATGAAATATGTATA[C/T]ATATACACACATATA | 23072 |
rs372432093 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43382121 | AAACCCCGTCTCTAC[C/T]AGAAAATACAAAAAA | 23072 |
rs372452404 | snp | C/G | 4.97492e-05 | 0.0049872 | intron-variant | HECW1 | GRCh38.p7 | 7:43541307 | CAGCCCTGTCTGCAG[C/G]GCAAGGACACCGACC | 23072 |
rs372459753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43386209 | CAGATTGAAAGAATT[G/T]GTGTGATTCAGTCAG | 23072 |
rs372461521 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43353238 | TAAATAAGAAGAAAC[A/G]TTAATGATTTAATAT | 23072 |
rs372467890 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43461868 | TCTCTCCAGATAAAA[C/T]AAAACTGAAAGAAAG | 23072 |
rs372476016 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115299 | CCAACTCAAACAGGT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs372479307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425883 | TCAACATGAGTTTTC[A/G]TAGGGATATTCAAGC | 23072 |
rs372507793 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512583 | ATAATCATTAATAAA[A/C]ATTAGATGAATTTAA | 23072 |
rs372508793 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149163 | CCCCTTAAATACGTA[C/T]TGATTACAAAGAAAA | 23072 |
rs372510937 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190914 | CCAAACTGGAGTCTG[C/T]CTCAAGTATTAATAC | 23072 |
rs372511922 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43414257 | TTTGGCTCTCTGTTT[A/G]TCTGTTGTTGGTGTA | 23072 |
rs372517665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162517 | ATTTAGGATCCACCT[A/G]AATAATCCAGGATGA | 23072 |
rs372522946 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43285226 | CCTGGGATTAGATAT[A/G]TAGACAAACTGGATC | 23072 |
rs372527219 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43371846 | TGTTTTGAGACAGAG[A/T]TTCGTTCTTGTTGCC | 23072 |
rs372537374 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43254261 | AAGATCTTTTTTTTC[-/C]AGTGGAGAATCAATG | 23072 |
rs372539819 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248625 | CATTAATTCTCTACA[C/T]TTATTGATTTGGAAC | 23072 |
rs372543043 | snp | A/C/G/T | 0.186421 | 0.24178 | intron-variant | HECW1 | GRCh38.p7 | 7:43556697 | TGTCTCAAATTAAAT[A/C/G/T]AAAAAAAAAAAAGAA | 23072 |
rs372558760 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43357143 | GGGAATGTAAATTAG[C/T]ACAGCCACTATGAAA | 23072 |
rs372559294 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43304575 | AGCTCACTGCAGCCT[C/T]CACCTCCCTGGTTCA | 23072 |
rs372568404 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180550 | ACAGGTGCCCGCCAC[C/G]ACGCCTGGCTAATTT | 23072 |
rs372580826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43499734 | TCCTTTGAAGCATGC[A/G]TACGATAGAAAGATT | 23072 |
rs372585805 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347579 | AAGAGGAGTGGTGAG[A/C]GTGGTCATCCTTGTT | 23072 |
rs372590757 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516225 | TAGTCACATACTTGG[C/T]GCTCAGTAAATATGT | 23072 |
rs372609976 | in-del | -/GAGA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247779 | AGAGGAAAAAAGAGA[-/GAGA]AAAAAAGAAAAGAAG | 23072 |
rs372611263 | in-del | -/GGA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43284538 | AAGACAGAAACAGAA[-/GGA]AGGAAGGAAGGGAAA | 23072 |
rs372611971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303152 | AGATTTCAGCAACTT[C/T]GCTGCTGAACGCCTC | 23072 |
rs372615283 | in-del | -/AAGC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43472409 | TTGTGGCAGGATTTT[-/AAGC]TTTTTAAGAACAGAA | 23072 |
rs372615571 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43219267 | CATTTGCATATCAAA[G/T]GTTGCCAGCTAGGCT | 23072 |
rs372616325 | snp | C/T | 0.000420149 | 0.0144879 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43442625 | CACTTCCTCCATCCA[C/T]CCAGGTATTTTCAGC | 23072 |
rs372622944 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283166 | TTCTCGGTGTACAGT[G/T]TGGGGACCCCTGGAA | 23072 |
rs372624037 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43498668 | TGGACACTGCTGCTC[C/T]CTTTTTCAACCCAGT | 23072 |
rs372627475 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43195036 | TGAAGGACTGTTTTT[-/T]AATGAGGGAGATTTT | 23072 |
rs372631250 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43380123 | CAGTGGTGTTATCAG[A/G]TTCACTGCAACTTTG | 23072 |
rs372632377 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43172075 | TTGAGGTCTGGCGTT[C/T]AAAACCAGCCTGGCC | 23072 |
rs372633298 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43338102 | ATTGAAACACAGAGA[A/C]CTACTCCAGTGATCT | 23072 |
rs372638656 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43200463 | CCTCTTCAGCAAACC[C/T]GGCAGCCAAGTCAGA | 23072 |
rs372639300 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355343 | GTAGGAAGCCCAAAA[A/G]ATAAATTGATCAAAA | 23072 |
rs372642771 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43221002 | TGCTGGAGAGGGACC[A/G]TTTGGGCTCAGCATT | 23072 |
rs372646031 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372326 | CCTTTTCTTTTTTAC[C/G]TGTTTATATTTACTA | 23072 |
rs372647486 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43323626 | CAAACACAACAACAA[A/C/T]GACAAAAATACATTA | 23072 |
rs372655617 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43240997 | CAGAGGAACTGGCTG[G/T]GTATAGCTGTGTGTA | 23072 |
rs372660466 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43346927 | AAATCAGGTAGTATG[A/T]TGCCTCCAGATTTGT | 23072 |
rs372665438 | snp | C/T | 4.99451e-05 | 0.004997 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445542 | AGGTCTGGAATCCCC[C/T]GTGGCAGGTCCAAGC | 23072 |
rs372676015 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123274 | AGCTACTCACAGTTC[A/G]GTCATTAAACAGAAC | 23072 |
rs372681819 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43203173 | CATGCCCAGCCCTCT[C/T]CTTGCCTTTTATACT | 23072 |
rs372690579 | in-del | -/GAGA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189609 | TAAAAAAAAGAAAGA[-/GAGA]AAACTTGACCTTATT | 23072 |
rs372695838 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43223389 | TTGGGAGGCTGAGGC[C/G]GGCAGATCACCTGAG | 23072 |
rs372697780 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43466986 | TTGATATGGTTTTTT[C/T]GAATATCGTGCTGAA | 23072 |
rs372698413 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166149 | AGTGAAGTGGTGCTA[C/T]CTCAGCTCACTGCAA | 23072 |
rs372701953 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189458 | ATTAAAATACAAAAA[A/G/T]AGATTGTGTGCAGGT | 23072 |
rs372713447 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160348 | TCAGAGCTCTCAATG[C/T]TTCACTTGTGTTGTT | 23072 |
rs372714179 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210297 | CATTGAAAAGGTGCA[C/T]TGTGATGAGGTGAGA | 23072 |
rs372715059 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118362 | GGGGGTTCAAGTCAG[A/G]GCAGTTGGAGAAACA | 23072 |
rs372719410 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372935 | CTACCCATCAACCCC[A/C]CAGCCATTCCTATGG | 23072 |
rs372722268 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43489138 | CAACAAATGTTTCCT[A/G]AGTCCAGTGCACAGC | 23072 |
rs372724057 | snp | C/T | 6.79937e-05 | 0.00583028 | intron-variant | HECW1 | GRCh38.p7 | 7:43542011 | CAGGTTTGTGTGACA[C/T]GGGGTTTGGAAAAGG | 23072 |
rs372728589 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43540304 | AAAACCTACTTAGAG[C/T]GGACACCAGGAAGAC | 23072 |
rs372731760 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138979 | GTGCAGACAGACTGG[-/T]TTTTTTTGTTTGTTT | 23072 |
rs372734838 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43267717 | AGAGAAAACAAATAT[A/T]CATGATTAGAATCAG | 23072 |
rs372744539 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43165021 | CTATATTTGTAACTG[C/T]TCCCTTGTTTCAGAA | 23072 |
rs372745174 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43180434 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 23072 |
rs372753752 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43307125 | ACTCCCATAGCAGGG[C/T]ACTTTGTACAGTGTA | 23072 |
rs372755821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43358090 | AAATCTAGTAGTGCC[C/T]GTTTGGGATTCCTGG | 23072 |
rs372757501 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43406455 | TAAATAAGTGCATAT[A/G]AAAACAACTGTGCTT | 23072 |
rs372775105 | snp | C/G/T | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118962 | AATATGCTTCAAAAA[C/G/T]GTTGTCCCACTGGCC | 23072 |
rs372783266 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144456 | CTTGAAAGCAGACAC[C/G]TACCTACCTATGGAA | 23072 |
rs372797598 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43530883 | CTATATCCTTCATAT[C/G]GGTGCAAAGTGATTT | 23072 |
rs372809597 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215190 | GTGACTGTATAGGCA[C/T]CGCCTAGTCAGAATG | 23072 |
rs372842236 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237755 | TCCAACTCCCTAAGA[A/G]CACAAGCAAACCACC | 23072 |
rs372846326 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43361610 | TCAGGCCTGTGGTAA[C/T]AGATGCCATCTTCCT | 23072 |
rs372848806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43481175 | ACGTGTTCACAGACT[A/G]CAGAAAGCAATGCCC | 23072 |
rs372860293 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307888 | TCACTATATATATAT[A/C]TATATATACACATAT | 23072 |
rs372866326 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213538 | GCAAGCTCCACCTTC[C/T]GGGTTCACACCATTC | 23072 |
rs372867151 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43528614 | AAGAGTCTGCATAAG[G/T]TACTTTTAGAAGTGC | 23072 |
rs372868058 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335940 | TTTCTTTCTTTTTCT[C/T]TCTTTCTTTCTCTCT | 23072 |
rs372874591 | snp | A/G | | | missense | HECW1 | GRCh38.p7 | 7:43463754 | GCAGGAGGAGGCGGA[A/G]GTGGAGGGAGTGACT | 23072 |
rs372876167 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519490 | ACTTCATGATTGGCC[C/T]GTCTCGGCCTCCCAA | 23072 |
rs372892233 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43199853 | TGGCATAAATTCTAT[A/T]TATACACGTTTGGTT | 23072 |
rs372902202 | in-del | -/GC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361059 | TTCTTGTGCGTGCGT[-/GC]GTGTGTGTGTGTGTG | 23072 |
rs372934180 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43261932 | GTCAGTAAAAAATTA[C/G]AAACCTGGTCCAGTG | 23072 |
rs372946242 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43559186 | ATCAACTGTGTAGAT[C/G]ACACAGTTAGAAGGA | 23072 |
rs372950634 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43370399 | TCTCATTCATTGCTG[C/G]TGGAAATGCAAAATG | 23072 |
rs372977947 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43498637 | GGCTTTCACATGTTC[A/C]CTGCTAAATGACATG | 23072 |
rs372984920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43549380 | TTATGGACTGCTTTG[C/T]TTAGGTACCTGTGTC | 23072 |
rs372989299 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43295153 | AAAAAAAGAAAAAAA[A/T]CAGGTATGCATTGTC | 23072 |
rs372997166 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43475749 | TATTTTTTTGGTAGA[G/T]ACAGGTTTTCGCCAT | 23072 |
rs373000882 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257006 | GCCCACTCTCTCTCC[A/C/G/T]TTCCCAAATTAACAG | 23072 |
rs373004259 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43239739 | TACACCCACTTAAAA[G/T]AAGTGTAAATTATTT | 23072 |
rs373021380 | in-del | -/AAAG | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43256849 | AACCTCCCTCACAAA[-/AAAG]AAAGAAAGTAAGGTA | 23072 |
rs373023451 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43485648 | CACAATGGTATTTGT[G/T]CCTCTAAACATATCT | 23072 |
rs373024030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203778 | ATCACTTTTTAATGG[A/G]TAATTGTGTATTGTC | 23072 |
rs373036412 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43502043 | AAATATTTACTCTCT[A/G]GTCCTTTGCAGAAAA | 23072 |
rs373038516 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43254337 | ACAGGTAATTGTTAG[A/G]GAGAAGAAATATGGC | 23072 |
rs373045445 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43466024 | GGGAGGGACAGAGGG[-/G]AAGGAAGGAAGGAAG | 23072 |
rs373055121 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43360523 | AAGATATTAATCACA[A/G]TGAATTAAATAATAG | 23072 |
rs373063715 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43336043 | TTCTTTCTTTCTCTC[C/T]CCTTCCTTCCTTCCT | 23072 |
rs373068120 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299170 | AATCATCGGTTTGCC[A/G]TCTGATAATTGCTAC | 23072 |
rs373076506 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494903 | AGCTTTTCCTTCCAG[A/G]GTATTCCACCTCCAC | 23072 |
rs373082546 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43490796 | AGAGTCTTGCTGTGT[C/T]GCCCAGGCTGGAGTG | 23072 |
rs373090671 | snp | A/G | 1.66977e-05 | 0.00288939 | missense | HECW1 | GRCh38.p7 | 7:43469100 | AAAACGGACCAGCAG[A/G]GAAAGGTGAGTGTGA | 23072 |
rs373091000 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43218848 | AATGACACGGACACA[C/T]GTGGAGTGGTTTTAA | 23072 |
rs373094979 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226360 | TCTTAAAATGAAGTC[A/G]GGAATATCTACCCTG | 23072 |
rs373096757 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43399037 | TTTTACAATACTGAC[A/G]TTATCTCCAGGAGCA | 23072 |
rs373098269 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43234508 | GCTCTCCCACCTCAG[A/G]CCTTTTTTTTTGCCT | 23072 |
rs373099210 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43505041 | TTCTGGGACACCACT[C/G]CAGACATCTCATCTA | 23072 |
rs373100106 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359784 | CATATTTGAGAAAAA[-/A]TATCTCAAATTGGAG | 23072 |
rs373108013 | in-del | -/ATTTT | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150377 | CCAGCATTTTATTTC[-/ATTTT]ATTTTATTTTATTTT | 23072 |
rs373117546 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43323948 | CTGAGGCAGGAGAAT[C/T]TCTTGAACCAGGGAG | 23072 |
rs373127884 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43344803 | TCTACTGTTAAACCT[A/G/T]TTCATTGAGTTCACT | 23072 |
rs373143586 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250123 | TTTTAACCAAAACAC[A/G]CACACACACACGCGC | 23072 |
rs373143646 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215544 | CGTTAACAAATGGTT[A/T]AGGTATTTTTAAACT | 23072 |
rs373150352 | in-del | -/ATTCAT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158315 | CTTTGAGATTCTTAT[-/ATTCAT]GATTTTGCTTAAGGG | 23072 |
rs373166856 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308617 | TACTAAATTATCATG[C/G]CTTTCTGTAATTTTT | 23072 |
rs373185388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43368815 | GGTTTACATCCTTCC[G/T]GTCTGGACTCTAAGA | 23072 |
rs373189341 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43402109 | GCTGAGAGCTACCTC[C/T]GCCAATCACTGAAAC | 23072 |
rs373193263 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43543799 | AAAAAAAAAAAAAAA[-/G]AAAAAAAAAGAAAAC | 23072 |
rs373193709 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378522 | AACCCTTGGCACTTT[C/G]GGCCAGGCATGGTGG | 23072 |
rs373197215 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43409709 | TGTCCCCCTGGTAAG[G/T]CTCAGGCTGAGGATA | 23072 |
rs373197625 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160524 | AATGTCCTAGAGGCA[C/T]GCGTTGAGTAATTCA | 23072 |
rs373199555 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43189838 | AAAATGTCAGTCAGG[G/T]TCACCTCACTGCCCA | 23072 |
rs373202102 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43178195 | TATTTTAGTAGAGAC[A/G]AGGTTTCACCATGTT | 23072 |
rs373211774 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43227373 | AGTTTACAAAGCTAA[C/T]AGTATTCAAATATAA | 23072 |
rs373234700 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43311536 | ACAAAACATGGAAAC[A/G]CAGGACACCCTGGTG | 23072 |
rs373241600 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162781 | CCCATACTACTGTAA[A/T]AATAACATTGTAATA | 23072 |
rs373248589 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43188117 | GGCAGAATGTGGTTC[A/C]AGACTGAGGATGTCT | 23072 |
rs373253695 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269776 | ATACAAAGCTGGGGG[C/G/T]GGGAAGTGAGGGTAG | 23072 |
rs373256741 | snp | A/G | 4.97459e-05 | 0.00498703 | intron-variant | HECW1 | GRCh38.p7 | 7:43396920 | CTGAGACTTTGTGGA[A/G]AGACTAAGAATGTCA | 23072 |
rs373265491 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179804 | CAGTGTTATATAAAA[A/G]AGCCTAAGGGAGAGT | 23072 |
rs373268912 | in-del | -/T | 0.204189 | 0.245767 | intron-variant | HECW1 | GRCh38.p7 | 7:43393677 | TTCTTTTTTTTTTTT[-/T]CATCTACAGACCTGT | 23072 |
rs373271990 | snp | C/T | 1.65603e-05 | 0.00287747 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43541223 | GTACCTTCTTGACGC[C/T]TTCTTCACGAGGCCC | 23072 |
rs373272170 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43208405 | AAAGGTGACATTCTT[A/G/T]TTTTAAGTGTTCTCT | 23072 |
rs373273608 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43279202 | CCAGCTGTGGGGACT[C/G]TGTGATAATGAACTG | 23072 |
rs373274587 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184435 | TACTATGAAATATGT[A/G]TTTGGTCTTCATCCC | 23072 |
rs373276817 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43221754 | GAGACAGGGTTTCAC[C/T]GTATTAGCCAGGATG | 23072 |
rs373279844 | in-del | -/GAGG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247754 | AAGGAGGGAGGGAGG[-/GAGG]AAGGGAAAGAGAGGA | 23072 |
rs373280999 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225022 | GAGTGTTTTGAGCAA[-/A]GAAATGACATGATTA | 23072 |
rs373293040 | in-del | -/GA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43185415 | GTCGGAACTGTCTCA[-/GA]ATTATAGGTGACAGC | 23072 |
rs373305174 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43558695 | GCTGCTCTCTAGTAC[A/C]TAAGGCCAGAAGAGG | 23072 |
rs373309652 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43181500 | CCACACCCCACCAGC[A/G]CTTGTTTTCTTTTAT | 23072 |
rs373310567 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488002 | AAAAAAGAAAGAAAG[A/C]AAGCCAGCCAGCCAG | 23072 |
rs373326288 | snp | A/G | 1.86416e-05 | 0.00305294 | missense | HECW1 | GRCh38.p7 | 7:43445504 | CTGGCCGCCCCTAGC[A/G]GGCACGTGGAAAGAA | 23072 |
rs373341777 | snp | A/C | 3.43424e-05 | 0.00414367 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43442560 | TACACACTTGGCCGC[A/C]GGCTTCCAACAGATC | 23072 |
rs373343667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43265371 | AGCGGGCCAGGAAGT[A/G]TCATCCTGCCTTGTG | 23072 |
rs373347388 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43398763 | GAGACCAGAGTTTTA[A/G]TATCACTCAAATCAG | 23072 |
rs373364953 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43533654 | ATAGACTAACGACTG[C/T]GTGCAGGGTTTTTAA | 23072 |
rs373367911 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43463089 | TAGTACTTGGCAAGG[C/T]GGCCAGCTGGCAGGC | 23072 |
rs373390212 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151980 | AAAGACATAAATTCT[A/G]TAGATCTCTAAACTA | 23072 |
rs373394582 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141904 | TGGAGTCTATGAGCC[A/G]GACACCTCAAGTCCT | 23072 |
rs373417422 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139378 | GCTACTGGCTTGGCT[C/T]AGAAATGTTCAAAAG | 23072 |
rs373436850 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319381 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 23072 |
rs373463402 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126614 | GTTTTATTGCATTTC[A/T]CTTTATTGCACTTCC | 23072 |
rs373472023 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43329804 | GGTGTGAAGGACTTT[G/T]TGTAGGGGGAGTGTA | 23072 |
rs373483525 | snp | C/T | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111569 | AAGCTGCCTTCACAT[C/T]GTCCAAAGTTTCCAG | 23072 |
rs373489838 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150377 | ACCAGCATTTTATTT[C/T]ATTTTATTTTATTTT | 23072 |
rs373493153 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141237 | AATCCACTGAGTGGG[A/G]TCATTAGGAAACTCT | 23072 |
rs373507213 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158042 | ACAGTGAAGTATAAT[A/G]TAAGGCTTTTAAGCT | 23072 |
rs373515264 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264234 | TTGACCAACATCTCC[C/T]CATCCCTCCCCCTTC | 23072 |
rs373525501 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43551293 | CCCTAACAAAACAAG[C/G/T]CTTCCCAGATCTCTA | 23072 |
rs373527822 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43325996 | ACACTGGGGAATTCA[G/T]AAATAATAGAAATTT | 23072 |
rs373529839 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43305012 | CAGAGAGGAAGCTGC[A/G]GGACTGAGAACAGTC | 23072 |
rs373537120 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372571 | TTCTAACAATAGATT[C/T]CTTTTTTAAAAAAAT | 23072 |
rs373544331 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43339959 | TTCAGTATTTGTGAA[A/T]GTCTGAGGGGAAACC | 23072 |
rs373555114 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480950 | TGAGAAACATAACTA[C/T]TTCCAACCAGTGGCA | 23072 |
rs373558924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427281 | GGAGGTGCCACAGTC[A/G]AATATGGAAGCACTG | 23072 |
rs373569931 | in-del | -/GT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43539765 | CCACAACCCTACTAT[-/GT]CATGTTAGAAGCATT | 23072 |
rs373576994 | snp | A/G | 0.000136689 | 0.00826594 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43554686 | ACTGCAGTTTGTCAC[A/G]GGAACATCCAGCGTG | 23072 |
rs373577547 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319606 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs373596328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43235447 | TGCGGAATAAGAGAG[A/G]CATCCTTGGCCCAAG | 23072 |
rs373602735 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43388347 | GTTCAGGACAAGAAC[G/T]GCAAATTCAAAAGCT | 23072 |
rs373606405 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43480245 | CTCTACAATGTGCTC[-/T]TTCCTTGGCAGCACT | 23072 |
rs373611748 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412744 | TTACTGAGAATGATG[A/G]TTTCCAATTTCATCC | 23072 |
rs373614285 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416692 | CGAGATTCCGTGGGC[A/G]TAGGACCCTCCGAGA | 23072 |
rs373619130 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481612 | ATTGAATAGCCCAAA[G/T]AGAGTTAATTTAATA | 23072 |
rs373642724 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173920 | TCAAAGCTCACTGCA[A/G]ACTACGACTCCTGGC | 23072 |
rs373646359 | snp | A/G | 0.000163986 | 0.00905352 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43463720 | AGATTCTGGCAGCCA[A/G]AGCTGCGAGCAAGCC | 23072 |
rs373650626 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | HECW1 | GRCh38.p7 | 7:43231895 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 23072 |
rs373655428 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180320 | GTGCACAAAAAACTT[A/C]AGGATTTTGAGTAAT | 23072 |
rs373664208 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43216783 | CTTCAGCCTCCCAAG[C/T]AGTTGGGATTACAGG | 23072 |
rs373678726 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43328995 | GATCTAGACATGCAG[G/T]CTCCGTCCCTGCATG | 23072 |
rs373679871 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226584 | CAGCCTGGCTTTTCT[A/G/T]TTCACAGACCAAACC | 23072 |
rs373680671 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43291445 | GGACATAGGCTGCAA[A/G]CTGGAACGTTCCTGT | 23072 |
rs373684685 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43385102 | CTGAATTCAAAGAAA[C/T]GGGTTCAGCCAAAGG | 23072 |
rs373701610 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43231302 | TGTAAGTCTTTTTTT[-/T]CTGGGCATTTACAAA | 23072 |
rs373704802 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43260651 | AATGATGGTGGCTTG[A/G]ACTAGTTGATGGTAT | 23072 |
rs373705177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43176772 | CTAAGTTTCCAACAC[A/G]TTGACTTTTGGGGAC | 23072 |
rs373707184 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136176 | ATGTGGGTTCTGCCT[A/G]AATCAGAGGCGCCTG | 23072 |
rs373708156 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43218921 | AAGAAGCTCCCCTGT[A/G]CAGAGACAGAGAGAG | 23072 |
rs373708317 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213321 | AGACTTTATCATAAA[A/T]GACATGTGCTTATTT | 23072 |
rs373714177 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43171771 | ATCCCTTCTCCCTGT[G/T]GTTGGCTACATTGCA | 23072 |
rs373717041 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43274275 | CCTAAATCATGTCGT[C/T]GCCAAGTCCCGCTTC | 23072 |
rs373719546 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127113 | GGCATGTCAAAAGCC[A/G]AGACAAGTCAAAAGC | 23072 |
rs373720552 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43243338 | TTGTGGTGACAGTCA[C/T]TCCGCAGGACAACAA | 23072 |
rs373727999 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43288827 | TTCATCTCACCCACT[A/G]TTGGTAATTCAGCTC | 23072 |
rs373739510 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43315023 | TGGGTATGGGCCATG[A/G]CACATCCGTGTGCCA | 23072 |
rs373742461 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43541319 | CAGGGCAAGGACACC[G/T]ACCTCTCTGGTGCCA | 23072 |
rs373744534 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157606 | CACTATGTCACTCAA[C/T]CTGGAGTGCAGTGGT | 23072 |
rs373752791 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468245 | TCATGTCCAGCCTTC[A/G]ATCCCCAGAGGCCCT | 23072 |
rs373755256 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43197125 | CCAGTGCACCTTTCT[C/T]TAAGGTGATGTAATC | 23072 |
rs373773879 | in-del | -/GAG | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43456544 | CTGCTCAGACTGTAT[-/GAG]GAGACTGGAAAGTAA | 23072 |
rs373779591 | snp | C/T | 3.31735e-05 | 0.00407255 | missense | HECW1 | GRCh38.p7 | 7:43561850 | GACTGGATCTTCCAC[C/T]GTATCCCTCGTACTC | 23072 |
rs373792271 | snp | A/G | 3.34152e-05 | 0.00408736 | missense | HECW1 | GRCh38.p7 | 7:43444398 | GTCCAGGGAACCAAA[A/G]CATAGAGCTTTCCAG | 23072 |
rs373793517 | snp | A/G | 0.000274231 | 0.0117064 | intron-variant | HECW1 | GRCh38.p7 | 7:43507985 | AGCATCCTGACTTCA[A/G]GGCCACTGCTCACCA | 23072 |
rs373794886 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43545737 | TCTATTCATTGAGTG[A/G]AAGTGGATCATCATA | 23072 |
rs373803383 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43474257 | GATCGAGACCACCCT[A/G]GCTAACATGGTGAAA | 23072 |
rs373821793 | snp | A/G/T | 3.38073e-05 | 0.00411129 | intron-variant | HECW1 | GRCh38.p7 | 7:43311714 | GTGATGACGGTGACT[A/G/T]AGTTGCCGGCGTGCC | 23072 |
rs373835514 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43532714 | ATCCCCTCAGCAATG[C/T]TGACACTCCCTGGCA | 23072 |
rs373837930 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43272563 | AAGCAGCCAGCAAAC[A/G]TATGAAGAAATGCTC | 23072 |
rs373839425 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43423217 | GCAGCCCTAAAGACG[G/T]CATTATTTCCCCAGG | 23072 |
rs373848437 | in-del | -/ATATA | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43308356 | ATATGATATATTTAT[-/ATATA]ATATAACATATAATA | 23072 |
rs373850109 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43246218 | TGAACAGGGAGAATC[A/G]CTTGAGCCCAGGAGT | 23072 |
rs373863433 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136781 | GTCAGCATTAGCAAT[G/T]CCCAGTGCTGTGCCT | 23072 |
rs373873799 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173017 | CAGTGGTTTCACACC[A/T]CATTGACAGAAGCCT | 23072 |
rs373878889 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363838 | TTCTGGTTAAGTGAT[C/G]ATTTGGCTATATGGT | 23072 |
rs373892537 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158317 | TTGAGATTCTTATAT[G/T]CATGATTTTGCTTAA | 23072 |
rs373897984 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43427985 | TTAATTCAAGGTCCG[C/T]TGTTTGGTAATCTAA | 23072 |
rs373898042 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130888 | AACTGGGTATACAAT[-/A]ATCTACTTAGTACTT | 23072 |
rs373899022 | snp | A/T | 0.000155988 | 0.00883003 | missense | HECW1 | GRCh38.p7 | 7:43445213 | TCCTGCTGCAGCCCC[A/T]CGTGCTACAGCTCCT | 23072 |
rs373913882 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43407125 | CTCCCTGGCAGCAGG[A/G/T]TTTCTCAGAACTCTC | 23072 |
rs373921142 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43385845 | AAAGTTAGCTCGTGG[G/T]TCTATAGGTCAGAAG | 23072 |
rs373927625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43170850 | TCAGAGTTGGCTGAG[C/T]TGAAAGTAGGGCGGA | 23072 |
rs373927824 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43402362 | TTCCTGCACCTGCCC[A/G]TCTGCATGCTCCCTC | 23072 |
rs373931011 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, utr-variant-5-prime, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113908 | GCTGGGCACCATAAC[G/T]TCTTCCCTGCCGAAT | 23072 |
rs373935438 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43415124 | GTTTCTTCCTAGTCT[C/G]GATGGTCTTTACATT | 23072 |
rs373938922 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467754 | GTCCACCGTGATCAC[G/T]AGTGGGTGCAAGATG | 23072 |
rs373947653 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488075 | AGCACTTTGGGAGAC[C/T]GAGGCAGGCAGATCA | 23072 |
rs373955380 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43432586 | TAAGACTCTGAGGTC[A/T]AAAGTTGGAGGCTGT | 23072 |
rs373957547 | snp | G/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508247 | TCTTCACCCCAATGC[G/T]ATTCTGATCACATTC | 23072 |
rs373963162 | in-del | -/TTT/TTTTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43401567 | TCTCATTTAAAAAGG[-/TTT/TTTTT]TTTTTTTTTTTTTTT | 23072 |
rs373976733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43314519 | AGAACAAAGAAGAGG[A/G]TAGTAGAGGAGGGGG | 23072 |
rs373978428 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154316 | CTTCCTGTTTAGTAG[A/G]TACAAGTTTGATATG | 23072 |
rs373980042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43503827 | GTGATAGTACCAGCG[A/G]TAGTGAAAATCATAA | 23072 |
rs374001592 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523800 | GATAAAAAGAAGACC[C/T]CCCCAATTAGTGGGG | 23072 |
rs374010949 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43492882 | GAGATCTGGTTCACT[G/T]TTAGTTTGATCCCTT | 23072 |
rs374015879 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43556295 | GGGGAATGGCAGCAC[A/G]TGTTCAGGAAGGTGC | 23072 |
rs374042953 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43406174 | CTTCCCTATGGTACA[C/T]AAGCCCTGGGTCTAG | 23072 |
rs374060432 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43255320 | AAGATTTATTCAGGC[C/T]GGGCCTGGTGGCTCA | 23072 |
rs374061853 | snp | A/G | 1.88475e-05 | 0.00306975 | missense | HECW1 | GRCh38.p7 | 7:43444499 | GCTGGGGAGCTCCTG[A/G]CCCAGGTGCAAAAGG | 23072 |
rs374067266 | snp | C/G | 1.65688e-05 | 0.00287821 | intron-variant, missense | HECW1 | GRCh38.p7 | 7:43450837 | CCGTAGGTGAATGTC[C/G]TATACTCCATAATTC | 23072 |
rs374073824 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43490231 | AGGTGGCTAACTGAT[C/G]AGACCATGTTCAAAT | 23072 |
rs374079467 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43228049 | AGGGTGAGTAAGCAG[A/G]GCTTTCCAAAATTAA | 23072 |
rs374081571 | in-del | -/CT | | | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43512981 | CCTCTTACACATTTT[-/CT]GAGTTCCCTCTAAAA | 23072 |
rs374084430 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529477 | AATTCTAAATCACAC[G/T]CCCTGACCTCAGAAA | 23072 |
rs374086047 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242880 | TCCAGTAGCGTCCAC[C/T]AGGGCGTTGGACACA | 23072 |
rs374088365 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300573 | CTTTATATTGCTAAC[A/G]GCCATGCCTGCTTCA | 23072 |
rs374092200 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43493023 | CAGCCATTTTCCAAT[C/T]ATCAGAGTGATTATC | 23072 |
rs374092215 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43375131 | TGCATTGAATTTACT[C/T]CAAAAGGAGCCAAGG | 23072 |
rs374095777 | snp | C/G | 0.000157988 | 0.00888644 | missense | HECW1 | GRCh38.p7 | 7:43445386 | CTCCTCGCAAGACGA[C/G]GAGGAGGAGGAGAAC | 23072 |
rs374096952 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43255592 | ACAAGAGTGAAACTC[C/T]GTCTAAAAAAAAAAA | 23072 |
rs374098288 | snp | A/C/T | 1.66418e-05 | 0.00288455 | missense | HECW1 | GRCh38.p7 | 7:43469089 | GCTGGGAGATCAAAA[A/C/T]GGACCAGCAGGGAAA | 23072 |
rs374100320 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43177126 | TATAAACTTTTTTTT[-/T]CTATGGCATTCAACA | 23072 |
rs374101009 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43475330 | GCACAATTGTAAGAA[C/G]AAAATCTTTGCCAGC | 23072 |
rs374103227 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224670 | ACAGAAAATAAAAAG[C/T]CGGCCATGGTGGCAC | 23072 |
rs374106666 | snp | A/G | 3.32602e-05 | 0.00407786 | intron-variant | HECW1 | GRCh38.p7 | 7:43501329 | ACTCCCCAGGTAACA[A/G]GAATCTGGCCTAATA | 23072 |
rs374106821 | snp | A/G | 7.05878e-05 | 0.00594045 | intron-variant | HECW1 | GRCh38.p7 | 7:43311610 | TGCAGCCTTTGTCAC[A/G]AGGAAGATGCTCTAT | 23072 |
rs374113162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439701 | ATGCTGAGTTCTCTC[C/T]TAAGTCCAAGCTGCC | 23072 |
rs374116206 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43314913 | TTTCATGAATGAGGA[C/G]ATGTCGAATCAGTGG | 23072 |
rs374118203 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43295098 | CAATTTACAGGAATA[A/G]TCACTTATGCCTTAG | 23072 |
rs374127234 | in-del | -/ATAAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355510 | TCTTTGTGATCTAAG[-/ATAAG]TTGTCATCTCCTTAA | 23072 |
rs374129669 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416493 | TTTTGTTTGTCTGTG[A/C]CCTGCCCCCAGAGGT | 23072 |
rs374131607 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43387453 | AAACTTTCCTTCTTG[A/C]TTCTGCCTGTATGTT | 23072 |
rs374141328 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43169691 | TCTTTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 23072 |
rs374143423 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43333984 | ACTGGGACCAGGAAA[C/T]GGATGTTAGAAAAGC | 23072 |
rs374145928 | in-del | -/CA | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297245 | GAACTGAATTAGATA[-/CA]GTCAGAGCAAGGGCA | 23072 |
rs374150952 | in-del | -/ATAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480684 | CACACATATATACGC[-/ATAT]ATATATATATATACA | 23072 |
rs374171293 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43390920 | CCTGGGCCTTGAAGC[A/G]TGACAAGATAAGGAG | 23072 |
rs374175243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43439089 | TATGGAGCTGCAGTC[A/G]CGTGTCACATGCAGT | 23072 |
rs374176307 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43318748 | CAGCATGTGAACTGC[A/C]GGGTGTCAGGAGAGA | 23072 |
rs374185953 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413052 | CCACAATGGTTGAAC[C/T]AGTTTACAGTCCCAC | 23072 |
rs374201161 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513683 | GTTTGTGGGTTTTGG[G/T]TTTTTTTTGTTTTTT | 23072 |
rs374211011 | snp | C/T | 1.65679e-05 | 0.00287814 | missense | HECW1 | GRCh38.p7 | 7:43311928 | GGCGTCACCATTCCC[C/T]GCTCCACCAGCGACA | 23072 |
rs374218261 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43353265 | ATATCCCTTTTCAGC[A/T]AGAATGGGAAATCAT | 23072 |
rs374239950 | snp | A/G/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43361054 | ATTTTGTTCTTGTGC[A/G/T]TGCGTGTGTGTGTGT | 23072 |
rs374262125 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43204378 | TTTTCTTGGTGCATT[C/T]GTTTGTCCAGCACTG | 23072 |
rs374263245 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327122 | TCTCAATCTGTGCTA[C/T]AATAAATACTTGGGC | 23072 |
rs374266725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225542 | AAATAAATTTTGGAA[C/T]ATACATCAAGGAAAT | 23072 |
rs374273665 | in-del | -/CTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544496 | TGTAGAGAAACAGAC[-/CTT]CTTGTCCATTGTAGG | 23072 |
rs374274396 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43286923 | ATTTGAAGAATTTGC[A/T]TACAATGATAGCAAT | 23072 |
rs374279913 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43258237 | AGTCCCAGCTACTCG[A/G]GAGGCTAAGGCATGA | 23072 |
rs374282089 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198729 | CAGATTTGCACACTC[-/TC]ACACCCCACACTCTC | 23072 |
rs374291337 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335334 | AGTCTAGCTGCTTGA[C/T]ACATATGAAGTGGTT | 23072 |
rs374292058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43551112 | CCAGAGGCTATAAAC[A/G]TTTTCTCAGGTCTTG | 23072 |
rs374299654 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43507517 | AGACAAAGGCATGTC[A/G]AAAATCACAGGGTAG | 23072 |
rs374300185 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158415 | AGGATCAAGTAATAA[G/T]AACTTACCCATTATC | 23072 |
rs374300769 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210802 | ACAGCAGACACCCTG[C/T]CAGATCCAGAGGGGT | 23072 |
rs374302030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43223615 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA | 23072 |
rs374310331 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43543506 | ACTCATGGCTGGGCA[A/C/T]GGTGGCTCACGCCTG | 23072 |
rs374320239 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43270035 | CACATTAGCATTGTT[C/G]TAAGCCCTGTTACTA | 23072 |
rs374325824 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43167563 | TTACAGAGGAACCTA[C/T]AAGAAGTGAAAGAGA | 23072 |
rs374326410 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336461 | GTGTGAGCCACCACT[C/T]CCAGCCAAGATTTGG | 23072 |
rs374327272 | in-del | -/TCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173815 | ACTCACAGTATCACC[-/TCC]ACCACCCAGGTGCCT | 23072 |
rs374331063 | snp | G/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299720 | AAGTGTCCCCTTCCT[G/T]TTAATGTTCTTCTAG | 23072 |
rs374337973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43310931 | TACTTTGATGAAGTC[A/G]GAATCACCCTTGCTT | 23072 |
rs374350080 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487572 | CCCTGAGAAACTTAA[C/T]AAGACCAAAGGGGTC | 23072 |
rs374354745 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43353784 | CCTGCCTCAACCCAC[A/G]AGAAGCATTGGGAGT | 23072 |
rs374354963 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43227472 | CACTAAGTGCAGAAA[A/G]TATGTAATAAAAGTA | 23072 |
rs374362113 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242407 | TTGGTTGGACAAAAA[A/G]GATGAAGAAAGAGGA | 23072 |
rs374372102 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43228399 | AAAAAATAATAGCAA[C/G]CTTGAGTAGATAAGG | 23072 |
rs374384580 | snp | C/T | 0.000554561 | 0.0166425 | missense | HECW1 | GRCh38.p7 | 7:43445259 | CCTGCTACAGCAGCT[C/T]GTGCTACAGCGCCTC | 23072 |
rs374385718 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43540395 | ATGCTAGACCAGGCA[G/T]GCAAGAAGCTGGTTT | 23072 |
rs374395562 | snp | A/C/T | 0.000155044 | 0.00880339 | intron-variant | HECW1 | GRCh38.p7 | 7:43407768 | AAAAAGCCCAAGTAA[A/C/T]AGTGAAAGGGCTGAC | 23072 |
rs374397852 | snp | A/G | 6.73469e-05 | 0.00580249 | missense | HECW1 | GRCh38.p7 | 7:43550550 | CGGGTGGAGCGCGGC[A/G]TGGTACAGCAGACCG | 23072 |
rs374398891 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120289 | CCTGCATCCTGACCC[C/T]CTTTATCAGATATCA | 23072 |
rs374406084 | in-del | -/CAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43418716 | CCTATCTATATTCAT[-/CAT]AAGTTAATATTTTCC | 23072 |
rs374421148 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43488265 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 23072 |
rs374426645 | snp | C/T | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111771 | TTATTCTAGAGGAGG[C/T]GGAGTTTGGGGTCTG | 23072 |
rs374431388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153294 | AGTGTTCTTCTGCTG[C/T]CTGGTCAGCATTGGA | 23072 |
rs374435338 | snp | A/G | 1.65652e-05 | 0.0028779 | intron-variant, missense | HECW1 | GRCh38.p7 | 7:43450888 | CTTCCCTGAGGCCTG[A/G]ACATCATCACTACCC | 23072 |
rs374446405 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43534582 | CCTACTGCAGCTATT[A/G]GAAATTTGAGCAATT | 23072 |
rs374450219 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43396705 | TGAAATCACTGTCTT[C/T]GTTGCCTGTAGCTGG | 23072 |
rs374460567 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214240 | ATGGATGTACATACA[C/T]GTAAAATTAGAGAAA | 23072 |
rs374462965 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43539019 | TTTCAAGTAACTTTC[C/T]AGTTTGTAACCAAAA | 23072 |
rs374465715 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HECW1 | GRCh38.p7 | 7:43381742 | TTGGCTAGGCTGGTC[A/G]CAAACTCTCGACCTC | 23072 |
rs374470288 | in-del | -/AGGAGAATGGC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481891 | TCGGGAGGCTGAGGC[-/AGGAGAATGGC]GTGAACCCGGGAGGC | 23072 |
rs374475449 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43257367 | TTTTCTAACCTATCA[C/T]CTAGTAACTCATGAT | 23072 |
rs374478915 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145226 | TCAATGTAGTCTGCA[C/T]GGCCCCTTAAGATGA | 23072 |
rs374480589 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192748 | TTAATAGATATCTTT[C/T]CCCATCTGTTAAGGT | 23072 |
rs374482624 | in-del | -/CA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198061 | CATAGTCACACACCC[-/CA]CACACACACTCTCTT | 23072 |
rs374489291 | snp | A/G | 0.000115918 | 0.0076122 | missense | HECW1 | GRCh38.p7 | 7:43479680 | CTCTTCAGAACGGTC[A/G]TCTTCCCAATCATCT | 23072 |
rs374491420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43191838 | TATTATGCAGTAGAA[C/T]AGGAGGACTGATGGA | 23072 |
rs374492006 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43342748 | TTATACATAGAGGCC[G/T]GGCATGGTGGCTCAC | 23072 |
rs374495139 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179480 | TTACTGGTACCTGAA[C/T]GTCTTAACATGGCTA | 23072 |
rs374504139 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43236372 | AAGTGTCTGACACAG[A/G]TGTCAGTCAATTTAG | 23072 |
rs374508740 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43380185 | AGCCTCCTGAGTAGC[G/T]AGGACTACAGGCACA | 23072 |
rs374516282 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43322537 | CCCCAACATAAACTC[A/G]CCCTCAGCCCACAGC | 23072 |
rs374517256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163428 | ACCCTTGTTCTGTCC[A/G]GGGGGAGGTGCTGCG | 23072 |
rs374519088 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184248 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT | 23072 |
rs374521665 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43357031 | AAATGCAAATCAAAA[C/T]CACAATGAGTTATCA | 23072 |
rs374544480 | in-del | -/AG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488487 | GAAAGAAAGAAAGAA[-/AG]AGAAAGAAAGAAAGA | 23072 |
rs374592506 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43420887 | TTGATCTGTGGTTTC[A/T]GCGATATCCTAATCA | 23072 |
rs374596746 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556489 | CCCAAGAGTTCAAGA[C/T]CAACCTGGGCAACAG | 23072 |
rs374601262 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179992 | AAATAATCAGACATC[C/T]CCAGCAACCTTAGAT | 23072 |
rs374614130 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43331501 | GGGAGGCTGAGGCTG[C/G]AGAATGGCGTGAACC | 23072 |
rs374619384 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43236328 | CCATTCATGGGGGGG[-/A]AAAGCTCAAATGAAA | 23072 |
rs374633518 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43401567 | ATCTCATTTAAAAAG[G/T]TTTTTTTTTTTTTTT | 23072 |
rs374635875 | in-del | -/GGCTCCTGGG/TTGCCCAGGATTACTTTCACTGCACTGTGGCTCCTGGG | 0.354235 | 0.227234 | intron-variant | HECW1 | GRCh38.p7 | 7:43180213 | GCTGGTAATGAATGT[lengthTooLong]TTGCCCAGGATTACT | 23072 |
rs374668786 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363605 | GAGAGAAATCCTGGG[C/T]TCCTATTGTCATGGT | 23072 |
rs374683763 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43310319 | TCCCTGGCCTTCAGC[A/G]CTTTGCCAGTCTTCC | 23072 |
rs374685327 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43545510 | TAGGGCGCTGAGTCC[C/T]GTACAGTTGAAAATT | 23072 |
rs374687796 | in-del | -/ATATA | 0.104504 | 0.2033 | intron-variant | HECW1 | GRCh38.p7 | 7:43308198 | TTATAATATATTTAT[-/ATATA]ATATATTTTTATATA | 23072 |
rs374690324 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43397072 | ACCACATAAGGATAA[C/T]AGAGAGTTTAGGAAG | 23072 |
rs374698936 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43333485 | TTACTTATTCCCTAC[A/C]GAAAATTTGAGGAAA | 23072 |
rs374709758 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43501674 | TTCTCTACAAAAAAA[-/A]TTAAAACTAAGCCAA | 23072 |
rs374730956 | snp | A/G | 3.31214e-05 | 0.00406935 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43552290 | GATAGCTGGCACCGC[A/G]GAAATCGACCTAAAT | 23072 |
rs374731902 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43263646 | TTACAGGCATAAGCC[A/G]CTGCTCCTGGCCCTG | 23072 |
rs374733389 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43548106 | GCCAGTGGCACCATG[C/T]ACAGGCTCTAAGTGT | 23072 |
rs374736951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43211053 | TGCAGTGCTCTCAGG[C/T]GATAGATGATTGGCT | 23072 |
rs374741243 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225344 | CCCTTTGGTGAGCAC[A/G]AAGGCCCCACCTAGC | 23072 |
rs374743365 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43364257 | TGCATCAATTCTTTT[C/T]CTCATTGTCTTGTTC | 23072 |
rs374744935 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237142 | AAGGAAGGAAGGAAG[G/T]AGGTAGGTAGGTAGG | 23072 |
rs374756959 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43306379 | AAAGATAAGCTTTGA[-/T]TTTTTTTTTTTTTAA | 23072 |
rs374760923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43430875 | CAACCTCTGCCTCCT[A/G]GGTTCAAGCAATTCT | 23072 |
rs374771774 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43255258 | AAGTACTGTTCCAGG[A/T]ACTACATTACCTTAT | 23072 |
rs374775594 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43169750 | CTAGAGTACAGTGGC[A/G]TGATCTCGGCTCACT | 23072 |
rs374784972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43224638 | CAGCCTGGGCAACAC[A/G]GCAAGACCCTGGCTC | 23072 |
rs374788708 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43355062 | CCTCCCAGGAATTCC[A/G/T]TATCCAGCAAAGTTA | 23072 |
rs374791111 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43239356 | TTGCAAGGGTGTCTA[G/T]TGTGACATTTCAGGA | 23072 |
rs374794252 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152173 | ATGTGAAAATACTTA[C/G]GAAATATTCTGTTAA | 23072 |
rs374795238 | in-del | -/CT | 0.952238 | 0.0903157 | intron-variant | HECW1 | GRCh38.p7 | 7:43343115 | TGTGCTGATCTATCT[-/CT]GTCTAATTCATCAAC | 23072 |
rs374797253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427139 | AGTTTTGTGGACATA[G/T]AACTCTAGGTTGACA | 23072 |
rs374800384 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293165 | GCGGAGGTTGCAGTA[A/G]GCCGAGATTGTGCCA | 23072 |
rs374806838 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210112 | GCGGACCCAGCCGTA[A/T]GTGGGGTGTGAGTGC | 23072 |
rs374811661 | snp | A/G | 1.68596e-05 | 0.00290336 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43561933 | CTTGAGTGAGGACAT[A/G]GAACCTCGCCTGACA | 23072 |
rs374813423 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43553126 | CTTCCTAAATACTCA[A/C]CTTGCACACTGCCAG | 23072 |
rs374821854 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43312329 | TCAGGTGTGGTTAAA[C/T]ACAAATGTCATTATC | 23072 |
rs374839676 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487825 | TTAGCTGGGCACAGT[A/G]ATGTGTGCCTATAGT | 23072 |
rs374855460 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43258366 | AAAAAATAAAAAAAA[A/T]AAAAAAATAAAAAAA | 23072 |
rs374879034 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129015 | TTATGGATGAGCAAG[A/G]AAAGTGATTTCTTGA | 23072 |
rs374890533 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43201882 | CAAGTATAGATAAAG[C/G]ACTGACTAAAATAAT | 23072 |
rs374898911 | in-del | -/TAAAGAAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43276030 | AGGAATAAGGAGGTT[-/TAAAGAAT]CAATTGTGCAGAAGG | 23072 |
rs374902297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43345368 | AGTCTATGGTTGGCA[A/G]TCTCTTATCAGAAGA | 23072 |
rs374907278 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159918 | TGTCCTGACCTCGTG[A/T]TCTGCCCGCCTCGGC | 23072 |
rs374909037 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43281674 | CTGCCTTCAGAATTA[A/G]ATCCTCCTCTTTCTT | 23072 |
rs374917908 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413239 | ATGTGTTTTTTGGCT[A/G]CATAAATGTCTTCTT | 23072 |
rs374919831 | snp | A/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43537736 | GCTTAGAGTCATCCC[A/G/T]TCTGTGGTTATGTAA | 23072 |
rs374924783 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43181174 | TTGTGGCAAATGACA[C/G]CATTTCATTCTTTTT | 23072 |
rs374925907 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43486762 | ATCACTGTATGAACA[A/C]TATGTAATGAATGCA | 23072 |
rs374929582 | snp | G/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508436 | AATTTAAAAAACTCT[G/T]TCTCTTAAAGTGCAT | 23072 |
rs374941747 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43227648 | TTCTGTTAATTGACA[-/T]TTTTTCTTACTTGAA | 23072 |
rs374947756 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43425606 | TTATAAATAAAAGAA[A/G]TTTATTCAGCTCACA | 23072 |
rs374957696 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43378912 | ACAAAATAAAAAACC[C/T]TTTGCGCTTTGAACA | 23072 |
rs374959981 | snp | A/C/T | 4.97222e-05 | 0.00498589 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43396843 | TGGTGCTGATGAGAC[A/C/T]GTCCAAGGACAAGGA | 23072 |
rs374976373 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43191245 | CCAGTGATGGTGTCA[G/T]TAAGAGGCCAGAGTT | 23072 |
rs374976461 | snp | A/G | | | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512286 | TTGGCCTGCAGGAAG[A/G]ACAGAGGTGCCTTAA | 23072 |
rs375001997 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43470756 | CACACACACACACAT[-/AC]AAATGGTCTCAGCAA | 23072 |
rs375005547 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125042 | GGAAATCCAACCCAG[A/C/T]GTGGTCGGGTTCTGT | 23072 |
rs375019839 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43390512 | TGCTACTGCATCCAG[A/C]CTGGGTGGCACAGCA | 23072 |
rs375036690 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43312227 | CTGAAGACCACTGTT[G/T]CATGACCTTGTTTTT | 23072 |
rs375038744 | snp | A/G/T | 0.000134604 | 0.00820285 | synonymous-codon, missense | HECW1 | GRCh38.p7 | 7:43444699 | GGAGCAGGAGGAGGA[A/G/T]GGAGATGTGTCTACC | 23072 |
rs375039475 | snp | A/C | | | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43249267 | CCTGGTGAGTCGCTC[A/C]CAGCCTGTCCCAGTA | 23072 |
rs375047170 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43484701 | TATTTTGGATTGTCC[C/T]TTACCTCACCTGGAA | 23072 |
rs375065932 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43251719 | TAATTAAAACCCAGC[C/T]GATGCTCTGGTTATT | 23072 |
rs375080619 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468127 | ACCAACCCTGTGTAC[C/T]GTCACATTGTCATTT | 23072 |
rs375094916 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422928 | ATCGCAGTGCCTGGC[C/G]GAGAGTCGTGGTCTC | 23072 |
rs375102457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358938 | CCAGCAATTCTCCTG[C/T]TTCAGCCTTCCGAAG | 23072 |
rs375115908 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43218207 | GGGCCATTCAGTGTA[A/C/G]GATATATTTAGATCA | 23072 |
rs375121201 | snp | C/T | 0.000420822 | 0.0144995 | intron-variant | HECW1 | GRCh38.p7 | 7:43466614 | CTGGCTCGGCAAGAC[C/T]CAAAACACAGCTTTG | 23072 |
rs375123424 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43317554 | TGGATTTCTGCAGCT[A/G]ACCCTGTCAATGCAG | 23072 |
rs375124866 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43346241 | TTGCATTTCCCTGAT[A/C]ATTAGTGATGTTGAG | 23072 |
rs375125016 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43265841 | AAAACTCCCCCCTCA[G/T]GTTCAATGATCTGCT | 23072 |
rs375128655 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43168115 | AAGTAGATTTGTGTA[C/T]GTGTCGTGAGGAGAG | 23072 |
rs375136077 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190929 | TCTCAAGTATTAATA[C/T]CATTCTGTGAAAGAC | 23072 |
rs375141065 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260561 | AATTTGTGTTTGAAA[A/C]ATTCTGGATAAAGTA | 23072 |
rs375150002 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237832 | CAATTCACCAGTCTT[C/T]CCCCCCCGCCGCCCC | 23072 |
rs375155761 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180170 | GACATCACCAACTTA[G/T]AGCAGAGGTTATGTG | 23072 |
rs375157058 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429315 | ATATATATATATATA[C/T]ATATATATATATATA | 23072 |
rs375166174 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293255 | AGAAAAGAAAAAAAA[-/A]GAAAATGAAAGTACA | 23072 |
rs375184327 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141944 | TTCCTCCCACTGGCT[C/G]TAATTTAGGCTTTGA | 23072 |
rs375185299 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HECW1 | GRCh38.p7 | 7:43166269 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTTGCTAT | 23072 |
rs375193224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43195917 | TCCCAGAACTGTCAC[A/G]GGGTGGTGGGTGTGT | 23072 |
rs375210446 | in-del | -/AATA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43230719 | ACATATGTATGTATA[-/AATA]TGTATACGTATATAA | 23072 |
rs375214060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43233312 | GGACTTTTTAGATTC[C/T]ATTATGGTAAAGACA | 23072 |
rs375235756 | snp | C/T | 1.69175e-05 | 0.00290834 | intron-variant | HECW1 | GRCh38.p7 | 7:43438195 | TTCCCACCAACAGGT[C/T]GTGCCCAAAGGTGGC | 23072 |
rs375238472 | in-del | -/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335980 | CTTTCCCTCTCTCTC[-/TC]TTTCTCTCTCTCTCC | 23072 |
rs375238971 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308266 | TATATTATATGATAT[A/T]TTTATATATTATATG | 23072 |
rs375248704 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43444070 | GAATTTTTCACTAGA[A/G]CTCTGGCCAGTGAGA | 23072 |
rs375260754 | snp | C/T | 0.100944 | 0.200705 | intron-variant | HECW1 | GRCh38.p7 | 7:43307931 | ATACACACACACATA[C/T]AGTGAAATGTATTAT | 23072 |
rs375279522 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HECW1 | GRCh38.p7 | 7:43485023 | GAAGGATAAGCAGAG[A/C]ACATAATTTTCATTT | 23072 |
rs375279794 | snp | C/G | 4.18261e-05 | 0.00457289 | missense | HECW1 | GRCh38.p7 | 7:43444598 | CTGCTGCTGGAAGAC[C/G]GTGAAGCCCCAGCCA | 23072 |
rs375280159 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43371979 | TGCCCACCACCACGC[C/T]CCGCTAATTTTTTTG | 23072 |
rs375282195 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43501871 | AAGAAAAGAAAAAAA[C/T]TAAGACAGTATTTTA | 23072 |
rs375289259 | snp | A/G | 5.37986e-05 | 0.00518618 | missense | HECW1 | GRCh38.p7 | 7:43550521 | AGGAGTACATCGAGC[A/G]CATGGTGAAGTGGCG | 23072 |
rs375289675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43347949 | AAGATTTTAGCATCT[A/G]TGTTCATCAAGGACA | 23072 |
rs375290263 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43240694 | GCATCAGGCCTCAGA[C/G]GTGGTGTCACTGCCA | 23072 |
rs375290406 | snp | C/T | 3.33868e-05 | 0.00408562 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509147 | TAATGTTCACTTTCT[C/T]GTATTTGAAAGTTCT | 23072 |
rs375292340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516643 | TCCTAGGAAGAATAC[C/G]AGCGCCTCAGACACA | 23072 |
rs375297108 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43465375 | ATCGTGGGTCAGCTG[C/T]GGAGTCGGCCACAGG | 23072 |
rs375309833 | snp | C/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335948 | TTTTTCTTTCTTTCT[C/G/T]TCTCTCTCCTTCCTT | 23072 |
rs375315570 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515759 | GTGAGATATGTTATT[C/T]CAACATTTTTAATAT | 23072 |
rs375316956 | snp | A/G | 1.65916e-05 | 0.00288019 | missense | HECW1 | GRCh38.p7 | 7:43360921 | AAATACTACCATGGA[A/G]TGAGTGGGGCCCTGC | 23072 |
rs375319269 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124307 | AAATAGCTTTTGAGG[G/T]ATCCAGATATTTTAT | 23072 |
rs375319781 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43320481 | CCCAATGGCGTCTTG[C/G]GGTGCTTCCTGCTCT | 23072 |
rs375330148 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146322 | CTAGTAGCAGCTGCA[C/T]CCACCCTACCCTCTC | 23072 |
rs375349623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43480409 | CTGACAATATCATGA[A/G]CAAATTTCTTTTTAT | 23072 |
rs375358030 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43366102 | GCAAGACTGTCTCAC[-/A]AAAAAAAAAAAAGAA | 23072 |
rs375358655 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269083 | TTAATTCATCCTCTC[C/T]CTCACCACTGAAATA | 23072 |
rs375361334 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43209262 | ACGGCACGCTGGCCC[C/T]CTGAAGACCCATGCT | 23072 |
rs375385570 | in-del | -/GG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173391 | TTGCCTCCAGTGGCT[-/GG]GTCCACCCCTCCCCA | 23072 |
rs375387015 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160972 | AACATCTCTCCATTT[A/C]TACAGGTTTTTTTTT | 23072 |
rs375395490 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133412 | TTTATGCCTTTTTCC[A/G]TATCAATCTGATAAA | 23072 |
rs375403568 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43427670 | CACAACCTGCGTTCT[C/T]GGCTCAGGATCTCAG | 23072 |
rs375403904 | snp | A/G | 0.000149409 | 0.00864187 | intron-variant | HECW1 | GRCh38.p7 | 7:43479764 | CCCTCCCTACACCCC[A/G]CCCTACTGTTCACCG | 23072 |
rs375404489 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43303490 | TTTTAACAAGTTCCT[C/T]GTATTTTAAATCATG | 23072 |
rs375404889 | snp | C/T | 3.31499e-05 | 0.0040711 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43312056 | AAAGGAGGAAGTGGA[C/T]GCTGGGGACTGGATT | 23072 |
rs375419423 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43449987 | GTATAAGCTATGTCT[A/G]TTGTAGGTTTTCTTT | 23072 |
rs375423208 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372547 | CCTTTTTTTAGACTT[A/G]TTTATGTTTTCTAAC | 23072 |
rs375430499 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43404901 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 23072 |
rs375453257 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359031 | AGGTTTCACCATGTT[A/G]GCCAGGCTGATCTCA | 23072 |
rs375456007 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237322 | AAGACCTGCCTGGAG[A/C]CCTCCTCGGCTCTTA | 23072 |
rs375456433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43386983 | TGGCATGCCAGGCAA[C/T]GCATTTGTTTTCCTG | 23072 |
rs375464479 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43469403 | AACCACTGTCTACAT[A/T]TTTTTTAAATTTAGG | 23072 |
rs375464510 | snp | C/T | 1.70994e-05 | 0.00292394 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43442577 | GCTTCCAACAGATCA[C/T]GTGAGTGGACAGCTG | 23072 |
rs375487519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43532906 | AGCCTTAGGGGTAAG[A/T]CCTGCATTGCCTCAG | 23072 |
rs375500282 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43548582 | TTAGGATTAGATTCA[G/T]CTACTAGTGAAGAAG | 23072 |
rs375549289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43478215 | TGAGGTCAGGAGCTC[A/G]AGATCAGCCTGACCA | 23072 |
rs375560641 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43531895 | TCCGCCTCTCCATCT[C/G]CACAAACTTCCTCCA | 23072 |
rs375568552 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187613 | GAAATTTTGATTTTA[C/T]GTGATTGAATTTGGG | 23072 |
rs375583279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43221720 | CACCACGCCCGGCTA[A/G]TTTTTTGTATTTTTA | 23072 |
rs375586370 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43194894 | AGACAGGGTTTCACC[A/G]CGTTGGTCAGTCTGG | 23072 |
rs375596966 | in-del | -/AAAA | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43374823 | ATATAATAACCAGTG[-/AAAA]AAAGATGAAAATATT | 23072 |
rs375601552 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43221028 | GCATTTAGTGCCTAC[C/T]TCTGCAAGACACTGT | 23072 |
rs375605797 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43236126 | TATATGCACTAGTCC[A/G]TGTATATACACACAT | 23072 |
rs375606163 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43402484 | GGAGAATTGTTTTAC[C/T]CAAGATTTCCATGTC | 23072 |
rs375621126 | snp | A/G | 1.68675e-05 | 0.00290405 | missense | HECW1 | GRCh38.p7 | 7:43445400 | ACGAGGAGGAGGAGA[A/G]CAGCGCGTTCGAGTC | 23072 |
rs375623447 | snp | A/G | 1.65938e-05 | 0.00288039 | intron-variant | HECW1 | GRCh38.p7 | 7:43552362 | AGGAGCTGTAATGAT[A/G]CAATGATCACAAATA | 23072 |
rs375627369 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43414856 | TGCTGGATTCGGTTT[A/G]CCAGTATTTTATTGA | 23072 |
rs375633706 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43315860 | GGAGATTTTTTCCCA[A/G]GATTTGGTTGTCAGA | 23072 |
rs375643537 | in-del | -/TGTGTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43241617 | TACTCTCCTAATGTA[-/TGTGTG]TGTGTGTGTGTGTGT | 23072 |
rs375655477 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43489288 | AATATTTTAAATACA[C/T]GTTAAGGCAAACTGG | 23072 |
rs375699485 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43202547 | GGTGCAATCTCGGCT[C/T]ACTGAAACCACTGCC | 23072 |
rs375702704 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43272179 | CTATCTCTCACCATA[C/T]GCAAAAATTAACTCA | 23072 |
rs375712580 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43399769 | TCTTACATTTATTCC[A/C]AGACAACCATTCCCA | 23072 |
rs375714495 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43217946 | CCTTCTGGGGCTGGA[A/G]AGTGCAGGATTTCCT | 23072 |
rs375715906 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179580 | CTCAGCAAAAACGAC[A/G]ACAACAACAACAACA | 23072 |
rs375717872 | in-del | -/AT/GGCAGGAGAAT | 0.433818 | 0.169443 | intron-variant | HECW1 | GRCh38.p7 | 7:43481888 | TACTCGGGAGGCTGA[-/AT/GGCAGGAGAAT]GGCGTGAACCCGGGA | 23072 |
rs375728519 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242111 | ATCCACTTTGCATGT[C/T]TGTATAAAGTAAGTC | 23072 |
rs375741614 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361696 | CTGATTAGGCTGAAA[C/T]GCACTGAGAAATGGC | 23072 |
rs375743884 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173034 | ATTGACAGAAGCCTC[C/T]GCGTTCAGACACCCA | 23072 |
rs375753925 | snp | C/G | 1.65721e-05 | 0.0028785 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43396870 | AGGAAGTCGGAGGCT[C/G]ATCAGCTTCTCTCTC | 23072 |
rs375759338 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43319304 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAAGCG | 23072 |
rs375786025 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43532357 | CTTCACTCTTGCCAG[A/G]CTCACCTCTCTCCAT | 23072 |
rs375791162 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43262915 | GCTTGATCTGAGTAC[A/G]AGGAGGTCGCTTCCA | 23072 |
rs375798536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157540 | ACAGGGTTTACATTT[A/T]TAAGGATAAAATTGA | 23072 |
rs375800649 | in-del | -/CCT | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43335365 | ATGGTGACCTTACAA[-/CCT]CGCTGCTATAGACTA | 23072 |
rs375820008 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43561247 | AGAGAGGACTGGCTC[A/T]CACGGGCAGCTTTTC | 23072 |
rs375823057 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43274876 | AAACAAACCACAAAC[C/T]AATGAAAAGTACTGT | 23072 |
rs375824831 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335769 | TTTCTTTCTTTCTTT[C/T]TTCTTTCTTCCTTTC | 23072 |
rs375828253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43210385 | GGGGCTCAGGTCATC[C/T]TGAGACAGGATTTTT | 23072 |
rs375831403 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412188 | ACATTGAGTTAATTT[C/T]GTACCACTTTACATA | 23072 |
rs375837231 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43434908 | TTCCTTGTGAAAATA[A/G]TAAGTGTTCATTATA | 23072 |
rs375845980 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43462854 | TTCATACTCCAGCTT[C/T]ACAATTTACAAACCT | 23072 |
rs375850656 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43312525 | CTTACTGCTTTGTAT[G/T]CAACAGACAAGCTGG | 23072 |
rs375861112 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43270877 | GAAAATCTTAGTTAT[A/T]AAGTACCTAGAGATA | 23072 |
rs375867375 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140349 | CCATAGAGGTGCTTC[C/T]TGACTGATGAGCGAC | 23072 |
rs375869932 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43244515 | GTTTACAGTCATCAC[A/C]GCTCACATTTACTGG | 23072 |
rs375869980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43528653 | AAAGAGAGGCACACC[A/G]CACACTTGGCCCACC | 23072 |
rs375870548 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43560547 | AACACCAGCATCCTC[C/G]CTAGATTCTCGATGG | 23072 |
rs375874919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43490507 | AGGATGAGTTACACT[C/T]TACATTAAATCCCAT | 23072 |
rs375878157 | snp | A/C/T | 0.0178166 | 0.092742 | intron-variant | HECW1 | GRCh38.p7 | 7:43180684 | ACGGGCGTGAGCCAC[A/C/T]GCGCCTGGCCAGTTT | 23072 |
rs375890040 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289638 | GGCCCATAGGTGGTC[-/T]TATTAACAGAAGAAC | 23072 |
rs375890360 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43258564 | AGAATGTCTCCAAAA[C/T]TGGATTAAGCCAGTG | 23072 |
rs375897153 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187909 | ACTGAATTTTTTCAC[A/G]TGTGCAACCATCTGT | 23072 |
rs375902111 | snp | C/T | 5.09732e-05 | 0.00504817 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43554716 | GCCCTACGAAGGCTT[C/T]GCAGCCCTCCGTGGG | 23072 |
rs375910588 | snp | A/G/T | 0.000133971 | 0.00818345 | synonymous-codon, missense | HECW1 | GRCh38.p7 | 7:43501228 | TCTCTTTGAAGAAGA[A/G/T]ATTATGTCCTACGTC | 23072 |
rs375912044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43462640 | GTTGGGGAACCTGTG[A/G]CCTAGAGAATAACAC | 23072 |
rs375913671 | snp | A/C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43559328 | CTCCAAAACATCCAT[A/C/T]GCACCAAGTGTGAGA | 23072 |
rs375914979 | snp | A/G | 1.66468e-05 | 0.00288498 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43492110 | CAGAGGAGCCTCTTT[A/G]CTGGCCAGGCCAGGA | 23072 |
rs375919260 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43232258 | ATTTGTGCCAGAACC[C/T]GTCCTCCACTGGTGA | 23072 |
rs375922158 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43451672 | TACCATTCTAGCTTT[A/T]ACTTCATAATACTCC | 23072 |
rs375925721 | snp | A/G | 3.33467e-05 | 0.00408316 | intron-variant | HECW1 | GRCh38.p7 | 7:43450786 | TGATGATGTTGCCAC[A/G]GCAGTGAATGAATCT | 23072 |
rs375927337 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43484082 | CTGCAGACAGGCGTT[C/T]CAGCTCCGGCATGTC | 23072 |
rs375944422 | snp | G/T | 3.42607e-05 | 0.00413874 | intron-variant | HECW1 | GRCh38.p7 | 7:43469142 | GGCTTTCATCAAACA[G/T]GCTCCTTCCCCAGGG | 23072 |
rs375948910 | snp | A/G | 4.97179e-05 | 0.00498562 | missense | HECW1 | GRCh38.p7 | 7:43444314 | GCAGTGGGGAACCTC[A/G]GTCTGAGGCACCAGA | 23072 |
rs375949221 | snp | A/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124055 | GAACTGAAGGGAAGC[A/T]TCAAGCTCTAAGATA | 23072 |
rs375974681 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287511 | GTTCTTTTCATTTTC[-/T]TCTTTGTTTGGAGAC | 23072 |
rs375975642 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287517 | TTCATTTTCTTCTTT[G/T]TTTGGAGACAGGGTC | 23072 |
rs375986974 | snp | C/T | 3.31702e-05 | 0.00407235 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43438113 | AAAGCTGTCGATGCC[C/T]GTTCAAAGACTCCTG | 23072 |
rs375997264 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519554 | TGGCCTAGTGCAGAC[C/T]TTTAAAAGCTATGCT | 23072 |
rs376000354 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122923 | TTGCTTATTTATTCC[A/G]AAAACATTTCTTGAG | 23072 |
rs376006171 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43166502 | GTGGAGATGGATGAG[A/G]GAAGGCTGACCCCTG | 23072 |
rs376017909 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123233 | ACAGAGTGAGCTCCT[C/T]AATTTTACAATATTG | 23072 |
rs376025723 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43439121 | TTTGCACTTGCCATT[C/T]ATGGTTGTGAGGATT | 23072 |
rs376039655 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129948 | AATGACAAGAAAAAG[C/T]CTGTACATGTTCATA | 23072 |
rs376041632 | in-del | -/TA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308268 | ATTATATGATATATT[-/TA]TATATATTATATGAT | 23072 |
rs376054820 | in-del | -/GT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43456044 | AATTTTAACATAGGT[-/GT]TGATCAAGGAACCAC | 23072 |
rs376055057 | snp | A/T | | | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295741 | TTATATCCCACTATC[A/T]CTCAGTCTCATAGCT | 23072 |
rs376062168 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43235327 | CCTCTGTCCTCCCAG[A/C]CTGCACTTCAGACCA | 23072 |
rs376073462 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43464682 | AGCAATGCAGAATAT[C/T]GGACATTTTCATGTG | 23072 |
rs376075834 | snp | A/G | 4.10872e-05 | 0.00453232 | missense | HECW1 | GRCh38.p7 | 7:43445076 | CTGGCCACTCCGGGG[A/G]CCACTTCCCCAGCCT | 23072 |
rs376081189 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43447442 | GCACTGGCAGTTTCT[A/G]AAGAAATATCTAAGT | 23072 |
rs376081419 | snp | A/C | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519669 | GGCAGGGGAATGGTT[A/C]AATGTATTACAGCAG | 23072 |
rs376086103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43419259 | TGCAGTGACTGTGGC[A/G]GCATTCAGGGCAAAG | 23072 |
rs376095997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43234564 | TGGACACTTCCTTTT[C/T]TTCCTTCAGGTCTTT | 23072 |
rs376099106 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422533 | ACGCCTGGTTAATTT[C/T]TTTGTATTTTTAGTA | 23072 |
rs376102773 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515266 | TTCCCAGGCGTTTGG[A/G]TTTTGTCATGAAGAT | 23072 |
rs376113794 | snp | C/T | | | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163561 | ACCATATGCCAGTTA[C/T]CCAGGGAGCTTGCTA | 23072 |
rs376124683 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529167 | ATCCTACTGTCAATC[A/G]TTCTACAGCCGGCGT | 23072 |
rs376127148 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43200731 | GCTTCAGCTGGGTAA[G/T]AGAAGAAACAGGGTC | 23072 |
rs376135651 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43178793 | ACCAGAGCCGCTGTG[G/T]CGTTCCTCAACTCCA | 23072 |
rs376138803 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283144 | AAAAAAGAAAGAAAG[A/G]AAGAAATTCTCGGTG | 23072 |
rs376158399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517520 | AATTGTAGAGTTTTA[C/T]GGAACTTAAGAAGTC | 23072 |
rs376160876 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43448287 | CTAGTATTCTTTTCA[A/T]ACTTTTTGCTTTATT | 23072 |
rs376164660 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143207 | AACTCCTGAACTCAG[A/G]TGATCCACCCACCTC | 23072 |
rs376167236 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43477422 | AATAATGAAAAGTCT[A/G]TTTTTAATATTTGTT | 23072 |
rs376187538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119480 | TTTAAATGCGGGTAC[A/G]GGGATTCCCCAGGCC | 23072 |
rs376189183 | snp | A/G | 5.12545e-05 | 0.00506207 | intron-variant | HECW1 | GRCh38.p7 | 7:43463623 | CCCAAGGAGCAAACC[A/G]AAGTTAACTCCTGTC | 23072 |
rs376228341 | snp | C/T | 9.94382e-05 | 0.00705048 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43438020 | ATTCAGTTTTGTGTC[C/T]TTGCCCACTGACGTG | 23072 |
rs376228688 | snp | A/C | 0.000165986 | 0.00910854 | intron-variant | HECW1 | GRCh38.p7 | 7:43466582 | ATGTGAGTGCCCTAA[A/C]ATGCAGAGGGGGCGG | 23072 |
rs376236106 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180380 | AAGTTTTATTTTATT[A/T]TTTTATTTTTTTATT | 23072 |
rs376240191 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43219134 | ACAGGGCGCCATGAT[G/T]TTCTACACATGTGGG | 23072 |
rs376242954 | in-del | -/AGAG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247774 | GAAAGAGAGGAAAAA[-/AGAG]AGAGAAAAAAAGAAA | 23072 |
rs376243323 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117993 | GGCTCTCCTGGTGTT[A/G]TCAGGCATCTATGCA | 23072 |
rs376243479 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154486 | TTCTAGGTCGTGAAA[A/G]TTTCCTCCATTCTCC | 23072 |
rs376257746 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146583 | GTCTTAATAAGTTGC[C/T]CAAGCATTACTGTAA | 23072 |
rs376261145 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127553 | AAAAAAAAAGGAAAA[A/C]AAACAGCCTTCTTGC | 23072 |
rs376262303 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226560 | GACAGGTCGAAAACG[A/C]CAGTAAAGCAGCCTG | 23072 |
rs376264211 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43205177 | CAACCTTCACCTCTT[G/T]GGTTCAAGAGATTCT | 23072 |
rs376280424 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43457764 | TGGGAGACAGAGTAA[G/T]ACTCCATCTCAAAAA | 23072 |
rs376294206 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43423641 | GTGAGCTGGGCAAGG[G/T]GTTAGCTTGGCACAT | 23072 |
rs376301153 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43445835 | TTGTATGTGTGCTTC[C/T]ATGTTTGTTTTAACT | 23072 |
rs376310181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43486196 | TGCCAAGGACACGAA[C/T]TCATCCTTTATTATG | 23072 |
rs376323664 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412823 | ATTCCATGGTGTATA[A/T]GTGCCACATTTTCTT | 23072 |
rs376328609 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517363 | TGCCCCAGCCCCGAC[C/T]TCTCTCCCTTCCCAA | 23072 |
rs376336459 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43545818 | TGGTCTTGTTGTCTC[A/G]GGGTGGAGGAGGTGG | 23072 |
rs376341643 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43539903 | CAGTTATGGGGTGGT[C/T]GGGAAAGGGCACCCA | 23072 |
rs376351931 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43430159 | TCATTTTTTCTCATA[C/T]CTCTCCCTAAATGAA | 23072 |
rs376375959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43402175 | CTGATTCTTCCTGGA[C/T]GCCAGACAAGGATCC | 23072 |
rs376383941 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43234151 | CAGCTCTCTTCTGTC[A/T]ACAATTCTGCCAAAT | 23072 |
rs376387800 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126124 | ACTGACGAGGATCAC[C/T]TTCCTATTTAAATGA | 23072 |
rs376389188 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123195 | ACCACGATGAATGAA[C/T]CCACAGCACATTTCT | 23072 |
rs376399595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43326090 | TGAGGGCCTGCTCAG[C/T]TTCAAAGACAGTGCC | 23072 |
rs376409392 | in-del | -/TCAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198160 | CTCTCACACTCATAC[-/TCAC]GCACACCCCACATTC | 23072 |
rs376412994 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43400820 | TCCAGAATGAATGTT[A/G]AGGGACTAAAATCAA | 23072 |
rs376418957 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43340012 | GTGCTGTAACTCTCG[C/T]CCCATCTAGTGAGCC | 23072 |
rs376438819 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359563 | AAATGATAGTTGGCC[A/G]TGCTTATTTCATAAT | 23072 |
rs376439018 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43321300 | TTCTGAATGTATAAA[A/C]TTTCTATCATATATC | 23072 |
rs376439163 | in-del | -/AAGG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43466041 | AGGAAGGAAGGAAGG[-/AAGG]GGGAAGGAGGGAGGG | 23072 |
rs376456782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43320192 | GTGGGAGGAGAGATG[A/T]TTCGAAGTGGAGTCC | 23072 |
rs376457917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43394752 | TGTCTAGACAGAGCC[A/G]ATTCATCAAGACAGG | 23072 |
rs376467156 | snp | C/T | 0.000198801 | 0.00996799 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43469045 | TTTCATCAACATGTT[C/T]GCAGACACTCGGCTG | 23072 |
rs376472802 | snp | A/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214781 | CCAGAAGGAGGAGGA[A/T]CCCCCAGAGAGGGGC | 23072 |
rs376480980 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43352867 | TTAATTGAACATTTT[A/G]CTTACTCAGGTCTCC | 23072 |
rs376488595 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43177701 | CACCTACTTCAACCC[A/G]TTTTGTGAAGGTTAA | 23072 |
rs376492128 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136187 | GCCTGAATCAGAGGC[A/G]CCTGATACTACTATA | 23072 |
rs376494065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43343729 | CCGCAATAAAAATAC[A/G]TGTGCATGTGTCTTT | 23072 |
rs376497772 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426103 | TGGGATGAGGAGGGT[A/G]TCTGGCCCCAATTAT | 23072 |
rs376519419 | in-del | -/GT | 0.000877016 | 0.0209222 | intron-variant | HECW1 | GRCh38.p7 | 7:43442677 | AGGCTAGTGTCATAA[-/GT]GTGGTTCCTTTTTCT | 23072 |
rs376521999 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343113 | GCTGTGCTGATCTAT[A/C]TCTGTCTAATTCATC | 23072 |
rs376524069 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160477 | TTTGACTTTATTTTG[A/G]TAAAAGAGAGATATA | 23072 |
rs376538646 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43424572 | AGGCTGCAGTGAGCC[A/T]TGATCACACCACTGC | 23072 |
rs376544006 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43233267 | CCCTCCATATCCTAT[-/C]ACCAACTAACATAAT | 23072 |
rs376545944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43232703 | TTACAGTGAACATCA[C/T]ATTTAATTGGCCAAA | 23072 |
rs376552794 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359406 | CCATTGTCCTAGGGA[C/G]AAAATTTGAACTTAA | 23072 |
rs376558675 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354187 | AAACATATCCAATAA[A/T]AAAAAAAAAAAAAGG | 23072 |
rs376558839 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43167479 | AAGGGATCCACTATT[C/T]AACAACTCCAGATGG | 23072 |
rs376564881 | snp | A/G | 0.000543478 | 0.0164755 | intron-variant | HECW1 | GRCh38.p7 | 7:43468899 | CCCACTCCTTACCCC[A/G]TCCGCCCTGACCTGT | 23072 |
rs376565095 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43240183 | CCATCTCTACTAAAA[A/C]TACAAAAAGCCAGGC | 23072 |
rs376567467 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43198870 | TTCTCCCAGGAGAAC[A/T]GGTGAAGTAGGAAGC | 23072 |
rs376571629 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43470119 | GAAAGGACATGTGTA[A/G]TAGAAAAGTCACTGT | 23072 |
rs376578808 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422073 | AGTACAGCGAGCTCA[A/G]GGTGTTTTCTAATGC | 23072 |
rs376583479 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43554388 | TTTTATAAAATGACT[A/G]TTTTCTAAATCTGCT | 23072 |
rs376586588 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139531 | CATATTTTCTCTTCT[A/G]TAACATTTAGTATTT | 23072 |
rs376591357 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150221 | GAAGTTCACATAGTA[A/G]TTTGTGAAACCAGGA | 23072 |
rs376592446 | in-del | CCTTC/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335927 | TCTTTCTCTCTCCTT[CCTTC/T]CTTTCTTTTTCTTTC | 23072 |
rs376607252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189987 | TTTCAGGAGCCAATA[C/T]TGGGAGAGAGAAAAA | 23072 |
rs376621823 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264979 | TTTTTTCTTATTTAC[C/T]GTGAAAACTTGATAA | 23072 |
rs376627595 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242919 | TCTCAGTACGTAGAT[A/G]TTGAATTCTCTCCGT | 23072 |
rs376642905 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43208704 | TAGGTCTAGGACATG[C/T]TCCTCTTAGGCAATT | 23072 |
rs376648612 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43171340 | AAGATTTCGTGTGCT[A/G]CTTTTATAAAATCTC | 23072 |
rs376650852 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43231754 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23072 |
rs376661071 | snp | A/G | 0.00013254 | 0.00813957 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43456394 | GGCAGCAGCCACCCC[A/G]GATGGCATGCGGAGA | 23072 |
rs376666956 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43482149 | TGGTAGCTTTTGGCT[C/G]ACAGAAGAGGACACC | 23072 |
rs376669273 | snp | C/T | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509087 | ACGGTGCAGATCAGC[C/T]CCATGTCCGCATTTG | 23072 |
rs376671477 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350764 | GACTATTTCTCCCTT[-/T]ACTTCTTGTATCATT | 23072 |
rs376684730 | snp | C/T | 3.39657e-05 | 0.00412088 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43554707 | ATCCAGCGTGCCCTA[C/T]GAAGGCTTCGCAGCC | 23072 |
rs376685968 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328996 | ATCTAGACATGCAGG[C/T]TCCGTCCCTGCATGC | 23072 |
rs376693201 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43113088 | TCTCGCTTCTCCCGC[A/G]AGGTTCAATTGTCAG | 23072 |
rs376695013 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43536585 | ATCGTTGGAACTTAG[A/C]CACACATGGGAAACA | 23072 |
rs376698165 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289030 | ATGGCCTACAACAGT[C/G]CCTGGCTGGTACTAG | 23072 |
rs376712177 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43498466 | TCATAAGGCCAAAAT[A/C]ATTAAATTAGAGAAG | 23072 |
rs376720812 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141561 | CTAGAGTGCAATGGC[A/G]CAATCTCAGCTCACC | 23072 |
rs376723506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43148980 | GGACAGTTCTTCCCT[A/G]CAGAAGAATTCCAAT | 23072 |
rs376724455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119789 | CCTGTGAGTCCCTCT[G/T]ACTTTTTTCTCACCC | 23072 |
rs376724770 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43194776 | TCGGCTCACTGCACC[C/T]TCTGCCTCCTGGGTT | 23072 |
rs376740439 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43384787 | AGTGGGTGGCTGGAA[A/C]GAGCTCTATGCAAAA | 23072 |
rs376742994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136664 | GAAGATTTCCAGCCC[A/G]TTTTCATCTAAATTA | 23072 |
rs376750415 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413318 | TTGTTTTTTTCTTGT[A/G]AATTTGTTTGAGTTC | 23072 |
rs376758597 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124436 | AGCCATTTGTAGATT[A/C]ATAGAATGCTGTCTG | 23072 |
rs376759873 | snp | C/G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43316668 | GAATGCAGAAAATAA[C/G/T]AGCCTCCTGGTAGAG | 23072 |
rs376771872 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43254282 | AGAATCAATGACCAC[C/T]GAGAGTAAAATAATG | 23072 |
rs376772391 | snp | C/G | 1.67871e-05 | 0.00289711 | missense | HECW1 | GRCh38.p7 | 7:43445286 | CCTCGTGCTACAGCC[C/G]CTCCTGCTACAACGG | 23072 |
rs376778741 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43480088 | TGAATACATGGAACT[G/T]CCATGGTATGTCTGA | 23072 |
rs376797229 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43197513 | GAGGGTGGGACCCAC[A/C]TCTTGGCACAGAGCG | 23072 |
rs376809452 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287362 | GGAGTGCAGAGGCCC[C/T]GAGGCAGGGTTGTGA | 23072 |
rs376819528 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43416383 | AGGAGGCAGTCTGCC[C/G]GTTCTCAGATCTCCA | 23072 |
rs376827994 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454589 | CTACATTTTTCCTTC[A/G]ATTTGTCTCATAAGT | 23072 |
rs376831928 | snp | C/G | 0.000347939 | 0.0131852 | intron-variant | HECW1 | GRCh38.p7 | 7:43311587 | CTGTCCCCGTGTGAA[C/G]CCAGAGCTGCAGCCT | 23072 |
rs376850601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520345 | GGAGTCTGGACTCCT[C/T]GGATTCTCAGGACAG | 23072 |
rs376852423 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198769 | TAGATTTGCACACTC[A/T]CTCACACACACTCCA | 23072 |
rs376870696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43536344 | ATTACACCGAAAACA[C/T]TGCCAGAGAGAGAGA | 23072 |
rs376876367 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511044 | AGCTTTATAGATGTG[C/T]CCGTTACACTTCATC | 23072 |
rs376883464 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43251973 | GGGTACATTCCACGG[C/G]GTCCTTGGCTTGACT | 23072 |
rs376891914 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43218944 | AGAGAGAGCAGTGCC[A/G]GGGAGCCAAGAGAGG | 23072 |
rs376892047 | in-del | -/AATTGAGTTTTA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43196884 | TTAAACTATGTTTTA[-/AATTGAGTTTTA]TTTTCCCCCTGCCCT | 23072 |
rs376895390 | snp | A/G | 0.000218364 | 0.0104467 | intron-variant | HECW1 | GRCh38.p7 | 7:43493190 | ACTCAGGTAAGCCTC[A/G]CCCCTCACTCCCTGG | 23072 |
rs376898424 | in-del | -/TA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361089 | GTGTGTGTGTGTGTG[-/TA]CGTGTACATACACAC | 23072 |
rs376910440 | snp | C/T | | | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43249275 | GTCGCTCACAGCCTG[C/T]CCCAGTAACTGTTCC | 23072 |
rs376910689 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43226898 | GGCTCCAGAACACAG[A/G]ATGGGGGCCATCTCC | 23072 |
rs376918837 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348177 | AATTTTTTAATTACC[A/G]TTTTAATCTCACTGC | 23072 |
rs376919947 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315045 | CGTGTGCCATCAAAT[A/G]TCCAGCAGAGGCCAG | 23072 |
rs376920821 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43217146 | GACAGCAACTTATTA[C/T]CGAGTACATGAAAAA | 23072 |
rs376923119 | in-del | -/CT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43257397 | TTAGTTGGGTACACT[-/CT]GGGAATCACTAACGT | 23072 |
rs376926888 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43233603 | AGCTTCCAAAATGGT[A/G]CAAAATAATACTTTT | 23072 |
rs376927435 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43286400 | TCCTCAAACCTTCAG[A/G]GATGTAGTGCAACCA | 23072 |
rs376965469 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117726 | CATCCCACAGTGTTT[G/T]GATGTGTGGGTATTG | 23072 |
rs376987922 | snp | C/T | 6.76041e-05 | 0.00581356 | intron-variant | HECW1 | GRCh38.p7 | 7:43311717 | ATGACGGTGACTGAG[C/T]TGCCGGCGTGCCCTG | 23072 |
rs376988550 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43457940 | TTCCCCATCAGCAGC[C/T]GAGTGTTTTAAGTCA | 23072 |
rs377000509 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43352021 | TTTATCCCCTTAACC[C/T]GGCAAACCTGTCAAA | 23072 |
rs377005543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147612 | GTTTTTAAGAAAACA[A/G]TAAATTTCTTTAGTT | 23072 |
rs377006312 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335524 | GCCCTTAGCAGAAAC[C/T]TGATCCACCAGCACC | 23072 |
rs377009531 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43549639 | TGATGACTCAAGCAT[A/G]TCCTAACAAACAGGC | 23072 |
rs377015811 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198691 | ACACACCACACACAC[-/AC]CATACATACACCCCC | 23072 |
rs377018753 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43442481 | ACTGCATGGTCATTA[A/G]GAAGAGAGGTATTGA | 23072 |
rs377020467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43493433 | CATTGATGTAGGGGG[A/G]GGAAGGACAGAAAGG | 23072 |
rs377023380 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43421263 | AGAAACCTTGAATGC[A/G]GTCTCACAACATACA | 23072 |
rs377035958 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142036 | TGCACTGGAGTCTGT[A/G]TTTATTTCTCCATTT | 23072 |
rs377044949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43405736 | TGAGCCACTCGTACC[C/T]GTTCTGGGAAGGTAG | 23072 |
rs377067544 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307964 | TATATTATATATACT[A/G]TATATCTTATATATT | 23072 |
rs377076969 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43532232 | TAAATTCCCTTGGCT[A/G]TATCTTGAGAATACA | 23072 |
rs377085639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43494573 | AGATGGTACAATCTC[A/G]GCTCACTGCAACATC | 23072 |
rs377086878 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43502676 | AAAAAACAAACAAAC[A/G]AAAAAAAAGATATTT | 23072 |
rs377091382 | snp | A/G | | | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563889 | AAAATAAATAAAAAT[A/G]AAAGCATTTTTTTAG | 23072 |
rs377093798 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43189047 | ATCTTACACTCGTTC[A/G]CTTCCTTTCTCACGG | 23072 |
rs377095481 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43243599 | TGTTTCTTGAAAAAG[A/G]AAAAAAAAAATTCTA | 23072 |
rs377095557 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43424370 | CACGCCTCTAATCCC[A/C]ACACTTTGGGAAGCC | 23072 |
rs377105577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43490576 | TGCCTCTATAGATTT[G/T]AACATCTTACTCTGC | 23072 |
rs377112251 | in-del | -/GAGA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247823 | AAGAAAAGAAAGAGA[-/GAGA]AAGGTAAGAAGGAAG | 23072 |
rs377124164 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43262050 | GTATGGTGAAACCCC[A/G]TCTCTACTAAAAACA | 23072 |
rs377126287 | snp | A/G/T | 0.000133663 | 0.00817415 | intron-variant | HECW1 | GRCh38.p7 | 7:43501364 | CTGTTAAGTGGCCAC[A/G/T]TGTGTTTCCTCCAGT | 23072 |
rs377137766 | snp | A/G | | | intron-variant, splice-donor-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298806 | CCGTTGCCACCACTT[A/G]CCACGAGGTGCAGGC | 23072 |
rs377147180 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335554 | CTTGACATTGAACTT[C/T]CCAGCCTTCAGAACT | 23072 |
rs377161341 | snp | C/G/T | 5.98478e-05 | 0.00547 | intron-variant | HECW1 | GRCh38.p7 | 7:43442651 | TCAGCATGAACTTCA[C/G/T]GTCTTGTCCTAGGCT | 23072 |
rs377167744 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43395406 | TGTCTCAGCCATAAT[C/T]TTGCAAAGGCAGCTT | 23072 |
rs377168307 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43357144 | GGAATGTAAATTAGT[A/C]CAGCCACTATGAAAA | 23072 |
rs377179792 | in-del | -/TG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260847 | TGATGAAGGAAACTG[-/TG]AAAAGGAGCAAGAAT | 23072 |
rs377200457 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43450445 | CTTTTGTGGAACCTT[A/G]TAAAACGCTGCATTT | 23072 |
rs377204476 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43191149 | GGGTTATATATATAT[-/AT]GCAAGAGGAAGGCAC | 23072 |
rs377207979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43365648 | TTATTTATTTACTTC[A/C]TATTCTGTATCTTCT | 23072 |
rs377208845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43323743 | ATAAAAAACAAATGG[C/T]TTGACCGTGCGCGGT | 23072 |
rs377214932 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43405161 | GAAAATGTATTTTAA[G/T]TGCTTAGAATGGTTC | 23072 |
rs377214963 | in-del | -/ACTC | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43198158 | CTCTCTCACACTCAT[-/ACTC]ACGCACACCCCACAT | 23072 |
rs377221948 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43439716 | CTAAGTCCAAGCTGC[C/T]GGCTCCTATCTTCTT | 23072 |
rs377223307 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43469428 | TTTAGGTTTGGAATG[G/T]GGAACTGAATTCTGT | 23072 |
rs377225923 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43491864 | CAAGTGCTAGGATTA[C/G]AGGCGTGAGCCAGAT | 23072 |
rs377231374 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155235 | ATGTAAATGTCCTTA[C/T]GAAGACACAATATGC | 23072 |
rs377232894 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247795 | AGAAAAAAAGAAAAG[A/G]AGGAGGGAAGGAAAG | 23072 |
rs377237204 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43439553 | AACAAAAACAGGGGC[C/T]GTGTGGGATTCTTTC | 23072 |
rs377260893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192981 | GGCTGGCTGTTTTTA[C/T]GGCTATTTCTTGATT | 23072 |
rs377262319 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224671 | CAGAAAATAAAAAGC[C/T]GGCCATGGTGGCACA | 23072 |
rs377268177 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43216058 | GAAGACAGAATTCCT[A/G]TTCTGTCTGTCATTT | 23072 |
rs377274818 | in-del | -/C | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268198 | TGGTTACTTTCTCCT[-/C]GGGGAAACAGACATT | 23072 |
rs377282815 | in-del | -/GTGACAATAACACCA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43238932 | AGGAAAATGAATTCA[-/GTGACAATAACACCA]TAATGTTATATAACA | 23072 |
rs377289355 | in-del | -/GCCATCCAATCT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43542126 | ATATCCACATTGTTG[-/GCCATCCAATCT]CCAGAACTTTTTCAT | 23072 |
rs377296396 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215335 | CAATCCTCACAGAAG[C/T]GTTGCCCTGTCCTAA | 23072 |
rs377299618 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546619 | ATTGTCCAATATCAA[A/C]AAAAAAAAAACAAAC | 23072 |
rs377301283 | snp | A/G | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298050 | TGAACTCCAGCCAGG[A/G]TGACAGGGTGAGACC | 23072 |
rs377301483 | in-del | -/GAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43211974 | TGTCTACTATGCAAG[-/GAG]TTCTTAAGGGAGACT | 23072 |
rs377314237 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43244210 | AAGTGAATTTGTACC[C/T]GGAAACATTCTATGA | 23072 |
rs377322294 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141578 | AATCTCAGCTCACCG[C/T]GCCTCCGCCTCCTGG | 23072 |
rs377329805 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120358 | CTCTCTTCCATCTGC[C/T]TGTTTGCTTGCTTTT | 23072 |
rs377332424 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127706 | GACATGAGCAAGCTG[C/T]AGAAGAAAAGTCTGA | 23072 |
rs377334745 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154884 | TTTAAAATTATGTAA[C/T]ATTTGATATGTACAG | 23072 |
rs377338972 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43534589 | CAGCTATTGGAAATT[A/T]GAGCAATTAACCTAG | 23072 |
rs377363194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43505129 | CCCAGGCTTTTTTCT[C/T]CACTCAAACTGTGTA | 23072 |
rs377368666 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43283813 | AAAGGATGCTTTTTT[A/G]ATGCAGCAATCTATT | 23072 |
rs377386173 | snp | A/G | 0.00113159 | 0.0237595 | intron-variant | HECW1 | GRCh38.p7 | 7:43311668 | CAGCTCACTCACAGC[A/G]CGTGTCTCCCAGCAC | 23072 |
rs377403732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43473561 | ATAAAATATGGGAAA[A/C]GTTGTATAATACAAA | 23072 |
rs377409078 | snp | C/T | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111865 | TGGGAAGGAATAAAT[C/T]AGCATTGTAGAGAAT | 23072 |
rs377431423 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43495555 | TCCTTGTCTTTGTGC[A/C]CACTCTGCCCCTTAC | 23072 |
rs377438031 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43382871 | TGCACCCATCAACCC[A/G]TCATCTAGGTTTTAA | 23072 |
rs377448453 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43412751 | GAATGATGATTTCCA[A/G]TTTCATCCATGTCCC | 23072 |
rs377449329 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43256894 | TATTGACAATCACTT[A/G]TTCAACTCTATTTAT | 23072 |
rs377457973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43467269 | AGGGAGGACAGAGTG[C/T]TCTGGGGGCGCCAGG | 23072 |
rs377461403 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43265650 | CCAGTTCCCTGAGAC[C/T]AACTGGGTATCCAAC | 23072 |
rs377464630 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43293923 | GATTTTCGTAGGAGC[A/G]TGAACCCTATTGTGA | 23072 |
rs377485853 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43449395 | TTTGCTCAACAAATA[A/G]TGTTCTATATTTAAC | 23072 |
rs377504483 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43254629 | CCCCCTTGCCTCCCC[C/T]ACCATTGTCAGCAGA | 23072 |
rs377506038 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115781 | CCTGAAATTACAGTC[C/G]CTGCAAGGCATAATT | 23072 |
rs377512268 | snp | A/G | 1.91977e-05 | 0.00309814 | missense | HECW1 | GRCh38.p7 | 7:43445510 | GCCCCTAGCGGGCAC[A/G]TGGAAAGAAGCCCGG | 23072 |
rs377525116 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43551790 | AGCAACAGACATTTT[C/T]TTCTCACAGTTTTGG | 23072 |
rs377530892 | in-del | -/GC | 0.0368353 | 0.130617 | intron-variant | HECW1 | GRCh38.p7 | 7:43542126 | ATATCCACATTGTTG[-/GC]CATCCAATCTCCAGA | 23072 |
rs377535375 | in-del | -/CTC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335366 | TGGTGACCTTACAAC[-/CTC]GCTGCTATAGACTAA | 23072 |
rs377535786 | in-del | -/TTTA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159105 | GCATGAATCTGACAG[-/TTTA]TTTATTTATTTATTT | 23072 |
rs377540770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360149 | TGTAAATAATGGAGC[C/T]GAAATTCAAACCCAG | 23072 |
rs377546362 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225182 | GATGGTGGCTGGACT[A/G]TTTTTCATGGTTGAA | 23072 |
rs377553517 | multinucleotide-polymorphism | CCTC/TTTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335933 | TCTCTCCTTTCTTTC[CCTC/TTTT]TCTTTCTTTCTTTCT | 23072 |
rs377560007 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43200145 | AGTTAACTTTCAAAC[A/G]GATTTGATTGGCCCA | 23072 |
rs377563272 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43252001 | ACTTGTAAGAATCTC[A/G]GCATCCAGCAGTATC | 23072 |
rs377563824 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43314920 | AATGAGGAGATGTCG[A/C]ATCAGTGGCTCCCAC | 23072 |
rs377574727 | snp | A/G | 3.90732e-05 | 0.00441985 | missense | HECW1 | GRCh38.p7 | 7:43444962 | AGGACTCCTCGGAGA[A/G]GGATGGGCTCAGCGA | 23072 |
rs377579443 | in-del | -/ACAAA | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43483375 | CCCCAAGTCATTATG[-/ACAAA]ACAAAACAGAACAGC | 23072 |
rs377593572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43350248 | CTGTCAATCTGATAC[A/G]TTTTCCTTTATAGTT | 23072 |
rs377597640 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43255672 | ATAAATATTTGTGAC[A/G]TGGCTCTTCTGGGCC | 23072 |
rs377604838 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43295183 | CTCGTGTGAGCAGAG[C/G]GACGACTTTGAGTTC | 23072 |
rs377609011 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43240255 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 23072 |
rs377612756 | snp | C/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298418 | ATGCACCCTTAGCAG[C/T]TTACAGTCCCCCTGA | 23072 |
rs377616985 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225678 | GATTATGAAACTATT[A/C]ATGCTACCAAAAAAT | 23072 |
rs377621686 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268228 | TTCCAACTCAGCTAC[A/G]GAATTAGTTACATAA | 23072 |
rs377623989 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43408078 | CCACAGCTCTTCCCA[C/T]GCATGTGATCCTTGA | 23072 |
rs377625831 | snp | C/T | 3.61768e-05 | 0.00425289 | intron-variant | HECW1 | GRCh38.p7 | 7:43444195 | TTCTGGGAGAAATGA[C/T]ATATTTTTCTTCTTA | 23072 |
rs377626716 | snp | A/G | 1.68233e-05 | 0.00290023 | intron-variant | HECW1 | GRCh38.p7 | 7:43469112 | CAGGGAAAGGTGAGT[A/G]TGACCCACGTGCGGG | 23072 |
rs377627129 | in-del | -/ACAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250149 | CGCGCACACACACAT[-/ACAC]ACACACACAGAAATA | 23072 |
rs377627246 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43450364 | AATCTGAAAAACAGC[C/T]TTTCGGCAGCCCTGT | 23072 |
rs377629818 | snp | A/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508589 | CCACCCACATACACA[A/T]ACACACACACACATG | 23072 |
rs377640728 | snp | C/G | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111241 | TTTTCTTTCAAGTCT[C/G]TGGTTGGAAACATCA | 23072 |
rs377641273 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180687 | GGCGTGAGCCACCGC[A/G]CCTGGCCAGTTTTAT | 23072 |
rs377642107 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127161 | ACAGTTAGCCAAGTT[A/G]TTAATACAAAGGAAA | 23072 |
rs377657344 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43227800 | TGAACAAAATGTGAT[C/G]CTGACTACAGAAAAA | 23072 |
rs377661156 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347841 | GACTTGCATATGTTA[A/G]ACCATCCCTACATCC | 23072 |
rs377677371 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43379855 | TCATTCATGGTGCTC[A/G]TGTTGTAATTGTGTT | 23072 |
rs377686213 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378810 | GACTGTCTCAAAAAA[A/C]AAAAATAAAAACAAA | 23072 |
rs377690948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43337201 | TGCAACCATGCCAAC[A/G]TCCATTGTTTTTTGA | 23072 |
rs377691724 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43350065 | GTGGTTTGGTAATGG[C/G]AAATTCTCTCAGCAT | 23072 |
rs377694512 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43322900 | TTTTAAGGTCACAGT[A/G]AAGTAGCAGTTCTCA | 23072 |
rs377699263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43502843 | GTTTGAAACATGTAG[A/G]AACATCCTATCTCAG | 23072 |
rs377701503 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127181 | TACAAAGGAAAAGTT[C/T]TTGGAGGAAATTAAA | 23072 |
rs377711212 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43272722 | ATACACTGCTGGTGG[A/G]AATGTAAATTAGTTC | 23072 |
rs377717656 | snp | A/C/G | 0.000252236 | 0.0112276 | missense | HECW1 | GRCh38.p7 | 7:43445001 | CGGTGGCCGCTGACC[A/C/G]GTCTGCCCTGGAAGA | 23072 |
rs377720223 | snp | C/T | 0.000165986 | 0.00910855 | missense | HECW1 | GRCh38.p7 | 7:43493084 | TTTTGTCTGTTTCAG[C/T]ATATAATGACAAGAT | 23072 |
rs377759958 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43193793 | TTTTGCCTGATGGCT[A/G]CAGGTTGACATTCCT | 23072 |
rs377763528 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43311092 | CATTTTTTCTCATCA[A/G]GTACAATGTTTTCTA | 23072 |
rs377763730 | snp | C/T | 3.56691e-05 | 0.00422294 | intron-variant | HECW1 | GRCh38.p7 | 7:43561775 | GAACCAGTTGTATCA[C/T]TGAAACAAACACTCT | 23072 |
rs386359800 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360230 | TTTTTTTTTTTTTTT[-/T]AAATGGAGTCTCACC | 23072 |
rs386410018 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264843 | GTGAGACTCGGTTTA[-/A]AAAAAAAAAAAAAAA | 23072 |
rs386410019 | in-del | -/AA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355619 | TAAAAATAAAAAGCA[-/AA]AAAAAACATACTACC | 23072 |
rs386410021 | in-del | -/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546241 | TTTTTTTTTTTTTTT[-/TT]TGCCATATCCACAGT | 23072 |
rs386712600 | multinucleotide-polymorphism | CG/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132173 | CTCACAGCGCCCCCC[CG/TT]CCCCAAGTAAGGTTT | 23072 |
rs386712601 | multinucleotide-polymorphism | GA/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155665 | ACCTCTCTACTCAGT[GA/TT]GTATTACCGTTTTGA | 23072 |
rs386712603 | in-del | GA/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43165683 | CACTCTAATCACTTA[GA/T]TTTTTTTTTAGTAAT | 23072 |
rs386712604 | multinucleotide-polymorphism | GC/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43184065 | GTTGCCCAGGCTGGA[GC/TT]GCAGTGGCTAGATCT | 23072 |
rs386712605 | in-del | AT/CAC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43191488 | GGCCCAGCTGTCACC[AT/CAC]GTGTGTGCTTATAAC | 23072 |
rs386712606 | multinucleotide-polymorphism | AT/GC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43209171 | CCAGCGTTAACAGTG[AT/GC]ATCAGACCCACTAGC | 23072 |
rs386712607 | multinucleotide-polymorphism | AAG/GAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43233523 | ATTTAGCAGGCCGAT[AAG/GAT]AGATTTTCCTGGATG | 23072 |
rs386712608 | multinucleotide-polymorphism | CGG/TGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237382 | TTCAGCTCATCTGTT[CGG/TGT]TGTGTCTCCCCTCCT | 23072 |
rs386712609 | in-del | A/CG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237839 | CCAGTCTTTCCCCCC[A/CG]CCGCCCCCACTTGGA | 23072 |
rs386712610 | in-del | C/GCCG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237840 | CAGTCTTTCCCCCCC[C/GCCG]CCCCCACTTGGAGCC | 23072 |
rs386712611 | in-del | CG/GCCC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237843 | TCTTTCCCCCCCGCC[CG/GCCC]CCACTTGGAGCCTGC | 23072 |
rs386712612 | multinucleotide-polymorphism | CT/TG | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247240 | ACAATGGAAGAAATA[CT/TG]CAGGAAAACTTGGTT | 23072 |
rs386712613 | in-del | AGAAAAG/GAA | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247788 | AAGAGAGAGAAAAAA[AGAAAAG/GAA]AAGGAGGGAAGGAAA | 23072 |
rs386712614 | multinucleotide-polymorphism | AC/TA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43252068 | TAGAATTCACTCCCT[AC/TA]ACACACAGAATATTT | 23072 |
rs386712616 | multinucleotide-polymorphism | CT/TC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289637 | TGGCCCATAGGTGGT[CT/TC]TATTAACAGAAGAAC | 23072 |
rs386712617 | multinucleotide-polymorphism | ACA/TTC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289831 | GTACATGGAAGGTGT[ACA/TTC]CTGGTTAGGCAGGAA | 23072 |
rs386712618 | in-del | GAACCCCACCTG/TT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327184 | CTACATGAGGAGACT[GAACCCCACCTG/TT]TGCAACGTAAAGGTG | 23072 |
rs386712619 | multinucleotide-polymorphism | AC/GT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43334516 | AAACAACCCTTATCC[AC/GT]TGCAGCAGCTACTAA | 23072 |
rs386712620 | multinucleotide-polymorphism | CTTTC/TTCTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43335913 | TTTCTGTCTTTATCT[CTTTC/TTCTT]TCTCTCCTTTCTTTC | 23072 |
rs386712621 | in-del | AA/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43342875 | CTAAAGATACAAAAA[AA/G]TCAGCTGGTCGTAGT | 23072 |
rs386712622 | multinucleotide-polymorphism | CCTGTGTACACAGTGACTA/GCTGTGTACACAGTGACTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378292 | AGGTGATTTTGCTCT[lengthTooLong]CTGGATGAGGAGAGA | 23072 |
rs386712623 | multinucleotide-polymorphism | AA/GC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43430907 | CTGCCTCAGCCTCCC[AA/GC]GTAGCTGGGATTACA | 23072 |
rs386712624 | multinucleotide-polymorphism | AT/GC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43433166 | TCCATTAATAAGAAT[AT/GC]CAACAAAAAATAAGC | 23072 |
rs386712625 | in-del | GACACCTGGGGGCATA/TTAGGAGCAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440087 | GGTGTCCCACCGTGG[GACACCTGGGGGCATA/TTAGGAGCAG]AGTGTTGGGGTGATG | 23072 |
rs386712626 | multinucleotide-polymorphism | CAA/TAG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43446237 | AAATGACTTTGTTTC[CAA/TAG]TAAGAATCAAATCCA | 23072 |
rs386712628 | in-del | GGT/TTGTTGATCTGTTTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467122 | ACAAACATTTTCTGT[GGT/TTGTTGATCTGTTTG]TCAGGCTCAGATCTA | 23072 |
rs386712629 | multinucleotide-polymorphism | ATC/CTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467360 | TCCAGGCAGAGGGAC[ATC/CTT]TGTAGAAAGGATGCA | 23072 |
rs386712631 | in-del | AGAAGTC/TATTTGGAATACTAT | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514256 | TGTGTCTTTGATGAC[AGAAGTC/TATTTGGAATACTAT]TTGGAATACTATTCC | 23072 |
rs386712632 | multinucleotide-polymorphism | CA/TG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43532728 | GTTGACACTCCCTGG[CA/TG]CATTCAGAAGGAATT | 23072 |
rs386712633 | in-del | CCTTCTGA/TCGTC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546088 | TCTAGATCTTCTTCC[CCTTCTGA/TCGTC]ACCTGGCACTGGTTC | 23072 |
rs397688972 | in-del | -/CT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43441565 | ATTCTCTCTCTCTCT[-/CT]GTTTTAGAACACAgg | 23072 |
rs397690981 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43369731 | GGACTTCTTAAACAA[-/A]AGGCTTTTCTCTTCT | 23072 |
rs397696589 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140130 | TGTTTCATATTTTTT[-/T]CCCCATTCACCTTGA | 23072 |
rs397735895 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43285011 | GATTTTTTTTTTTTT[-/T]GCTTTAAGGTTCTCA | 23072 |
rs397737430 | in-del | -/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147254 | GTTTTGTTTTTTTTT[-/TT]AACAGCACTCCAGGC | 23072 |
rs397741027 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43395054 | AGTTTGTTGATCTTG[-/G]TGGTGCCAGCTGATC | 23072 |
rs397747488 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43537553 | ACTAGAAGGTGTTTT[-/T]CTCATTCATGGAATT | 23072 |
rs397747651 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43456283 | TTCTTTTTGCCTTTT[-/T]TATTAAACACTAGAC | 23072 |
rs397748996 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43229644 | AAGTTAAAAAAAAAA[-/A]TTAATGGGCTATAAA | 23072 |
rs397772712 | in-del | -/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139816 | TCTTTGGAAAAAGGG[-/G]CAAATTTGGGGATCA | 23072 |
rs397781617 | in-del | -/CA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43470755 | TCACACACACACACA[-/CA]NTAAATGGTCTCAGC | 23072 |
rs397781860 | in-del | -/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520627 | TTGAATTATTTTTTT[-/T]ATTATTATTATTCTA | 23072 |
rs397785143 | in-del | -/TTG/TTGTTGTTG/TTGTTGTTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43446178 | TTGTTGTTGTTGTTG[-/TTG/TTGTTGTTG/TTGTTGTTT]GCTATTTTGGCTAAT | 23072 |
rs397788057 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43172439 | CTAGGATTTTTTTTT[-/T]CAATAAATTCTTTCA | 23072 |
rs397796319 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43548253 | TCTAACTTTTTTTTT[-/T]CATTTTAAAAAAGCT | 23072 |
rs397818699 | in-del | -/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43178315 | TGGCCAGCAGGGTTC[-/C]TATCTAACTATCCCC | 23072 |
rs397821651 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43369732 | GACTTCTTAAACAAA[-/A]GGCTTTTCTCTTCTT | 23072 |
rs397830613 | in-del | -/CT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43441553 | GTGTCTTTTTTTATT[-/CT]CTCTCTCTCTCTGTT | 23072 |
rs397835924 | in-del | -/AG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488421 | aagaaagagagagag[-/AG]aaagaaagaaagaga | 23072 |
rs397839920 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250111 | CTTGCAGATTTTTTT[-/T]AACCAAAACACACAC | 23072 |
rs397843139 | in-del | -/TAT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43327989 | tattattattattat[-/TAT]cattattattTTAGT | 23072 |
rs397890047 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361841 | TTTTTTTTTTTTTTT[-/T]ACATTAAAAAAAAAA | 23072 |
rs397890768 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43411046 | TTTATTGCCTTCTAT[-/T]TTTTTTTTTTTTAGC | 23072 |
rs397933557 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354200 | ATAAAAAAAAAAAAA[-/A]GGCCAGACAGAGAAG | 23072 |
rs397933964 | in-del | -/A | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131082 | CCAGCCTGGCCAATA[-/A]TGGTGAAACCCCATC | 23072 |
rs397935803 | in-del | -/ATTT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120649 | TTTATTTATTTATTT[-/ATTT]GTTTTATTTTTTGAG | 23072 |
rs397937624 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43234519 | CAGGCCTTTTTTTTT[-/T]GCCTGGAATATTCTT | 23072 |
rs397944957 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43349051 | TTTGTTTTGTTTTTT[-/T]GAGACGGAATTTTGC | 23072 |
rs397948741 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43527390 | GGAGACCCTTTTTTT[-/T]ACCTCTTTCAGCTTC | 23072 |
rs397948767 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43246153 | ATAAAAAAAAAAAAA[-/A]TTAGCTGGGCATGAT | 23072 |
rs397951396 | in-del | -/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159768 | CACTGCAAGCTCTGC[-/C]TCCCAGGTTCATGCC | 23072 |
rs397951703 | in-del | -/G/T | 3.3195e-05 | 0.00407387 | intron-variant | HECW1 | GRCh38.p7 | 7:43456284 | TCTTTTTGCCTTTTT[-/G/T]ATTAAACACTAGACT | 23072 |
rs397951978 | in-del | -/A | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513665 | AGCTGGAAAAAAAAA[-/A]CTGTTTGTGGGTTTT | 23072 |
rs397952940 | in-del | -/ATTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43409385 | CAAAAGAATTTATTT[-/ATTT]TGTATGGGGGGAAAG | 23072 |
rs397953467 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43246853 | GCAGAGCCTCTGCCA[-/A]GCCCAGTGGACTCTC | 23072 |
rs397957863 | in-del | -/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514315 | CTTTTTTTTTTTTTT[-/T]GAGATGGAATTTCGC | 23072 |
rs397959228 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43434051 | TTTTTTAAAAAAAAA[-/A]CAAAAAACCTTTTGC | 23072 |
rs397962573 | in-del | -/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43254261 | AGATCTTTTTTTTCC[-/C]AGTGGAGAATCAATG | 23072 |
rs397965922 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136080 | TCAACTTTTTTTTTT[-/T]CTCAGTTTATTCACC | 23072 |
rs397972311 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43446417 | GACTGGGAAAAAAAA[-/A]TTGAAAAGTCACATA | 23072 |
rs398004594 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43173276 | TGGCTAAGCAGAGGA[-/A]GAATGGTTTTGCTAT | 23072 |
rs398004597 | in-del | -/TA | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43307895 | ATATATATATATATA[-/TA]CACATATATATATAT | 23072 |
rs398004598 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43331606 | CAAAAAAAAAAAAAA[-/A]GATCAGGGTGAGCTT | 23072 |
rs398004599 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43343281 | TCTTTTTTTTTTTTT[-/T]AATTATACTTTAAGT | 23072 |
rs398004600 | in-del | -/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43365461 | ATGACATTCCCACCC[-/C]GTGTGGGGCCATCTA | 23072 |
rs398004601 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43373221 | TTTTTTTTTTTTTTT[-/T]CTTTTTGAGACAGAG | 23072 |
rs398004602 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375907 | AAAAAAAAAAAAAAA[-/A]GGAAAAAAAGCTCTT | 23072 |
rs398004603 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43411058 | TATTTTTTTTTTTTT[-/T]AGCTCCTTAGGGTAA | 23072 |
rs398004604 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43449796 | GAACCATCTGAAAAA[-/A]GGGCCATCCTTTGTC | 23072 |
rs398004605 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43457787 | TCAAAAAAAAAAAAA[-/A]CAAACAAAAAACATG | 23072 |
rs398004606 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524016 | CATCTTAAAAAAAAA[-/A]GATGAGGGACTTGGA | 23072 |
rs398004608 | in-del | -/GGTT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43533625 | GATGCCATAGTGGTT[-/GGTT]AGAAGAGGCCTTTAT | 23072 |
rs398004609 | in-del | -/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43551978 | ATCTAAGCACCCCCC[-/C]AAAGGCCCCACCTCC | 23072 |
rs398066824 | in-del | -/GTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361086 | TGTGTGTGTGTGTGT[-/GTGT]ACGTGTACATACACA | 23072 |
rs398085760 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43449795 | GGAACCATCTGAAAA[-/A]AGGGCCATCCTTTGT | 23072 |
rs398085761 | in-del | -/A | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513664 | AAGCTGGAAAAAAAA[-/A]ACTGTTTGTGGGTTT | 23072 |
rs398095041 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287472 | ATGGAAGGTTTGGCA[-/A]GAGGGGATGTGATCT | 23072 |
rs398095042 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43305401 | ATCTCAATTACTGCA[-/A]TTCTGTCCATCTGTT | 23072 |
rs398111286 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114739 | GTTCTCTTTTTTTTT[-/T]GGAGTAGTTTTTTCA | 23072 |
rs398111287 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117530 | TTGCTTTTCCAAGTT[-/T]AAGACACAATGAGAT | 23072 |
rs398111288 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127895 | TCCTTTTTTTTTTTT[-/T]AAAGACAAGGTCTTG | 23072 |
rs398111289 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180413 | ATTTTTATTTTTTTT[-/T]GAGATGGAGTCTTGC | 23072 |
rs398111290 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187342 | CCTTTCAAGTGGAGG[-/G]AAATTGGGCTCCACC | 23072 |
rs398111292 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376965 | TTAGTGAAAAAAAAA[-/A]GACTTTTCTTCAGGT | 23072 |
rs398111293 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43455800 | TTTGAGACCAGCCTG[-/G]CCAACCATGGCCAAC | 23072 |
rs527237609 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43338980 | ACTCAAAGTTAGGTG[C/T]TTTTCTCTTTAGCAC | 23072 |
rs527242120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43554418 | TCTTGTTCTAAAACT[C/T]GACCTGGTTGCACAA | 23072 |
rs527243301 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43491423 | ATGTAATCAATACTA[C/T]TTAAACAAGAAGTCC | 23072 |
rs527250722 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43272236 | AACTATAAGAATCCT[A/T]GAAGAAAACCTAGGA | 23072 |
rs527253549 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523723 | AGATGTACTTACTAA[C/T]GAGAGAGGCGCCGAA | 23072 |
rs527258564 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43187402 | ACGTATTTTGAACCA[A/C]CACATACCATAATTT | 23072 |
rs527264265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43231947 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 23072 |
rs527267363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513234 | TCTGTGGTTTTAAAG[C/G]CCTTGCAAAGTCAGT | 23072 |
rs527267985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43456149 | AGTGCCCCAGAAGTC[A/G]TGGTGGCAGGTGCTG | 23072 |
rs527277691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43363322 | TTCCATCACACTGTT[A/G]ACATAAGGTTCAGCA | 23072 |
rs527279110 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302555 | AGCCCTGCTGGGCTC[A/G]GGATGGAGTGAGGCT | 23072 |
rs527281592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150475 | CCTCTGCTTCCTGGG[A/T]TCAAGTGATTCTTAT | 23072 |
rs527301494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421641 | GCCACCACACAAAGC[A/G]GGGATGTCCAAATGC | 23072 |
rs527304556 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43496351 | GTGGACCCAGGTTGA[A/G]AACCCAAATATTTCA | 23072 |
rs527310854 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43496162 | GAACTTGAAATCAGG[C/T]CACGTTGGAATTGGA | 23072 |
rs527311498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192935 | ATAAAAGGGTGGCTA[C/T]TCCATAGGCAGAGCA | 23072 |
rs527320382 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43341731 | GTTAATATAACCAGT[C/T]CGTAATACAGCATTC | 23072 |
rs527330208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43278738 | TGCTTTTTCCCTTGA[A/G]GTCTAAGTTGTCACT | 23072 |
rs527344626 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43259722 | AACAGAAACTGAAAG[-/AA]AAGATTAGTGAACTT | 23072 |
rs527345896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369820 | ACAGAATAGACAAAA[C/T]GAAATGTTCACTTTC | 23072 |
rs527354277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43363948 | AATAAGCCTTTGCAG[C/T]CTCGTCTGGGGACTT | 23072 |
rs527361160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136816 | GAGCATTATAGTCAA[C/T]GCACGTCCACTCTCA | 23072 |
rs527365968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405435 | TTAGGGCAAAGTCTG[C/G]AGGAAGCCAGGAGCA | 23072 |
rs527368578 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43314092 | ATGCTGAGATTACAG[G/T]CATGAGCCACCATGC | 23072 |
rs527390259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43554986 | ATTATTCTTAGGGAG[C/G]TTTTGATGACTGATG | 23072 |
rs527403614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43272843 | CAAAAGAAAACAAAC[C/T]GTTACACCAAAAAGA | 23072 |
rs527423320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412116 | ACACGGCTTTGCGTT[A/G]CTTCCTTTGTAGTTG | 23072 |
rs527424880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143580 | TGTGAGCCATGGTGC[C/T]CAGCTGGATGCCTCC | 23072 |
rs527426553 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43548525 | TGTCAAGTTGTTAGA[C/G]AGTGGAGAGCAGAGG | 23072 |
rs527427289 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43323512 | CATCACCTGTACCGT[G/T]GAAGTTGAGGCTGCA | 23072 |
rs527431953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225258 | ACAAAGAAGGCTGGC[A/G]ATAGCAAGTACTGGA | 23072 |
rs527438145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129796 | CACAGATGCTCAAGT[C/T]GCTGGTATACGATGG | 23072 |
rs527439253 | snp | C/G | 1.65671e-05 | 0.00287807 | missense | HECW1 | GRCh38.p7 | 7:43500709 | TTCAGGGAGAAAATC[C/G]ATTACATTCGGACTG | 23072 |
rs527442396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43493826 | GTACATCTCTTTGAC[A/G]TTTGAATTTTCACTC | 23072 |
rs527458727 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43331905 | ACATTGAAGGGCAGT[C/T]TGATGGATTGAAGGC | 23072 |
rs527470876 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43225650 | CTATAATGTGAGGAA[-/C]TTTTAAAATTATGAT | 23072 |
rs527471331 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43447242 | CCTGTTTTAGTGCAC[A/G]GTTTTTTGGCCCCCA | 23072 |
rs527473244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43350138 | GCTTAGTTTCGCTAG[A/C]TACAAAATTCTTGGC | 23072 |
rs527478048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43541041 | TCCCTTGTGTCATCA[A/G]TGAGAAGATTCCTTA | 23072 |
rs527478274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43533068 | CCATCACTCTCCACC[A/G]CCAGTGGACACTGGC | 23072 |
rs527483485 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289128 | TTTTTTTTTGAGACA[A/G]AGTATCGATCACTCT | 23072 |
rs527497974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43212419 | TTTTAGCAAAATATT[A/C]TTTTCACTTTTTAAA | 23072 |
rs527499839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137611 | CTGGAGTGCAGTGGT[A/G]CAATCACGGCTCACT | 23072 |
rs527503166 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43219951 | GCCAGCCCTCCAGTG[C/T]GGTGCTGCTGGGGAA | 23072 |
rs527510229 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43287542 | AGGGTCTCACTATAT[C/T]GCCCAGGCTGGTCTC | 23072 |
rs527524531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43259352 | AGATCGCAGTGCTGC[A/G]CTCCAGCCTGGGCAA | 23072 |
rs527531902 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43164681 | CACTGGACTGGACTT[G/T]CCTTTTGGTGTGGAG | 23072 |
rs527536152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389004 | CCTGGACCAAGGTGC[C/T]AGTGATGGGGATGCA | 23072 |
rs527545112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43436434 | AGCTTTTTAATCACC[C/T]GGGCGCAGGCAGGCT | 23072 |
rs527561114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206346 | GAAGACAGGGGAGAG[G/T]AGAGGGAAATGGAAT | 23072 |
rs527572852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43391819 | TTACTTATCTACCAT[G/T]TACTTGTTTGAACAT | 23072 |
rs527572874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123421 | CTGCTTGCCGAGAGA[A/C]CACTGCTGTAGGAAC | 23072 |
rs527573348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43383483 | TGCCATTCTAACTGG[C/T]GTGAAATGGCATCTC | 23072 |
rs527582348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43399291 | AGCTTATAGGTTAGA[C/T]GCAAGATGGAGTTGG | 23072 |
rs527583135 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43418706 | ATATTTCTTACCTAT[C/G]TATATTCATCATAAG | 23072 |
rs527605679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43252920 | TCGAACAAGACAAAA[A/G]TGGTTAAGAGCTGAC | 23072 |
rs527611507 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43241143 | TCTGTGCACTCATTC[A/G]CTGCTGTCAGGCTGG | 23072 |
rs527616847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43301056 | TCTGTCCACCTTGCT[C/T]TCCCCCTCATTGCTG | 23072 |
rs527619514 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43343674 | TCTATCATTGATGGA[C/G]ATTTGGGTTGGTTTC | 23072 |
rs527623270 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43543527 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGAAGG | 23072 |
rs527624692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213015 | CATATTATTACAATA[C/T]TATATCAGTAAAAGC | 23072 |
rs527637960 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43196323 | TTGCAGGTATTTTAA[G/T]ATATAAAAAGGTAGG | 23072 |
rs527642944 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307812 | CAAAACAAAATAAAA[A/T]AAAAATGGGGTAAAT | 23072 |
rs527644497 | in-del | -/TAGGTA | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134945 | TTTTGCTAAAATGTC[-/TAGGTA]TAGGTATATAGGTTT | 23072 |
rs527668106 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43466201 | GAGGGAAAAGAAAAG[A/G]AAGAAAATCATTGTG | 23072 |
rs527668667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43355668 | ACAAAGGAAGATAGG[A/G]AATATGGAAAAAAGG | 23072 |
rs527673602 | in-del | -/GTGCTGC | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43206665 | CATACTGGGTGCTGG[-/GTGCTGC]GTGCTGCTTTTATTT | 23072 |
rs527681097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43355061 | GCCTCCCAGGAATTC[C/T]GTATCCAGCAAAGTT | 23072 |
rs527681195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43362474 | CATGCAGATTGGAAC[A/G]TGATTCCTGTCTGAC | 23072 |
rs527685538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43449209 | TTTTGTTTAATTTCT[A/G]ACACTAAACATGTAT | 23072 |
rs527693170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135245 | ATATTTGAATCTAAT[C/G]AGATAAATTTGGAAG | 23072 |
rs527693432 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43498533 | TGGTGTCAGGATTTG[A/G]AGGAGAAAGCCCAGG | 23072 |
rs527698306 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43202501 | TTTTTTGAAACAGAA[A/T]CTCACTCTATCCCCC | 23072 |
rs527711254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43306412 | CCCATTACCCACCTG[A/G]TGGCGTAACAAAGCC | 23072 |
rs527722694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43448580 | TACAAAAGCACTCTG[C/T]TTCCCACCAAGTGAG | 23072 |
rs527732653 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43472298 | ATGCCTGTCCTAACC[A/G]TCCAAGTTAATACCA | 23072 |
rs527735965 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43169553 | TCAGCCCAATTTCAC[C/T]TCTATGAGAGTAAAA | 23072 |
rs527745213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43539598 | ATCATTTATTTCATA[C/T]CTGCATATATTTACT | 23072 |
rs527747551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43442409 | GTTTTGTATTGCTGT[G/T]GAGCACATCAGGACT | 23072 |
rs527751975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43441480 | CTGGCACTGTCCATC[A/G]TTGAGGACATATTTG | 23072 |
rs527762865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43484476 | ATAGGGAATTAACTA[C/T]AGATATTTCTTAGAC | 23072 |
rs527766113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43204197 | TGTTGCTCCATCATT[A/G]TGTTAGTTCATTCTT | 23072 |
rs527772758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121511 | GCTCTGTGCTTTTCC[A/G]TAGTTGTGTAAACAT | 23072 |
rs527774513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389802 | TGCACCACCATGCCT[C/G]ACTAAATTTTTGTAG | 23072 |
rs527790316 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43443999 | TTTGAATCGTATTTC[A/G]GAAATATATCCATGA | 23072 |
rs527797517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43491994 | TCAAAATCTTTTACC[C/T]CTTAGGTTGAAAAAC | 23072 |
rs527799455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43258449 | TAACCCCAAGCCCCA[A/T]GTTTTTCTAGTGTAG | 23072 |
rs527806289 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43260351 | GTATATGCAAAGCCC[C/G]CATTGCAAAAGAAAA | 23072 |
rs527809010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43175844 | ACGTTTTCCTTCTCA[C/T]AGGCGCACCTCATTT | 23072 |
rs527810125 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43234514 | CCACCTCAGGCCTTT[C/G/T]TTTTTGCCTGGAATA | 23072 |
rs527812216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43348906 | GTTTTCTTAAATTTA[C/T]TGAGGCTCATTTTAT | 23072 |
rs527823722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43307240 | GGGCCACGTGATTAC[A/C]ACCAATAACTGGAAA | 23072 |
rs527826282 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43452915 | GTCGGGAGTTGGAAA[C/T]ACCCTGCTGGGTTTA | 23072 |
rs527856401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43292996 | TTGGGAGGCCAAGGC[A/G]GGTGGATCATGAGGT | 23072 |
rs527863398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43525513 | GAAACTGGAATGACA[A/G]GAGGGGTGGGCCCAT | 23072 |
rs527867960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163390 | TGTGCAGTGACAGAA[A/G]TGCTCATTGTGTGCC | 23072 |
rs527877123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43427508 | AACTGCATATTTGTT[C/T]AAAGTATATCTCTAT | 23072 |
rs527887162 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43292101 | TTCTCTTACAAAAGG[A/G]TAACAGTTTCAGAGC | 23072 |
rs527889968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43434888 | TAATAAAGGTGATTA[C/T]GTTTTTCCTTGTGAA | 23072 |
rs527899886 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237563 | CCTCCTCTGTAAAGT[A/G]TAGACAGTTATAGGA | 23072 |
rs527905774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43524789 | CACCTCTAGCTCTCC[C/T]GTGTGCTTGTAATAT | 23072 |
rs527906777 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43382060 | GGAGGCCAAGGCAGA[G/T]GGATCACGAGGTCAG | 23072 |
rs527908732 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43385420 | AATTTTGTGATTCAC[A/T]TCCTTGAGTATACAC | 23072 |
rs527911987 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43390382 | CGTTCCTACAAAAAA[A/T]TTTTTTTAATTTGCC | 23072 |
rs527913268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43251683 | ATGCTTTTGGAGTTA[C/G]GGGTTCATTACACTC | 23072 |
rs527926464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43475760 | TAGAGACAGGTTTTC[G/T]CCATGTTGCCCAGGC | 23072 |
rs527941834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149941 | GTAGTGGTCATAGAT[A/G]TCTTTTGGCATTGCT | 23072 |
rs527942591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157499 | AATAAATTACTGTGT[A/G]AAATTATGCAGTGAA | 23072 |
rs527945819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43469491 | CAGCTAACTCTCAGG[A/G]GATGAACTCATTGGT | 23072 |
rs527947452 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43239590 | TCTACAGCTTGGCAC[A/C]TCCTGCTGGAACTCA | 23072 |
rs527963026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115640 | TAGGCAGGCAGGCAG[G/T]GTTTTCATGCGCTAT | 23072 |
rs527965024 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43231718 | ACAAAATGTATTCTG[A/T]CATAAGAACCTCTTG | 23072 |
rs527975826 | snp | C/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513488 | CATTCTGGGCTTCCT[C/G]CTCCCTGTGTGTGGG | 23072 |
rs527981842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43199189 | ACGCCTGGTCTCTTA[A/T]GATTACAGTTTGCCT | 23072 |
rs527985337 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544400 | TTACAATTTTTTAAA[A/G]TAAATTAACGCTATA | 23072 |
rs527991757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43382494 | TTACAAAATACATAG[A/G]TTTCAACATCATAGA | 23072 |
rs527994502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43245366 | TTCCCCTTGGACTTC[A/G]GTGTTTTCTCTTTGG | 23072 |
rs528003285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43220823 | CTGGAACAAAGGAGA[G/T]AAGGGAGACCAGTTT | 23072 |
rs528003693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428154 | CCAACCCCACACCAG[A/C]TGAAAAGTTTCACTT | 23072 |
rs528022064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519491 | CTTCATGATTGGCCC[A/G]TCTCGGCCTCCCAAA | 23072 |
rs528028269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116551 | CCTGGGCCAGCCAAG[C/T]TTGACTGAGTCTCCC | 23072 |
rs528029701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43340630 | ATGCATTTTTTGATT[C/G]TTTTTGAATTTAGAA | 23072 |
rs528032639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43336114 | CTTTCTTCTTTCTTT[C/G]TTTCTTTCTTTCTCT | 23072 |
rs528034827 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43186311 | TAACTAGTACACACC[C/T]ACACCACATAACAAT | 23072 |
rs528052397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120760 | GTGATTTTTCTGCCT[C/T]AGCCTCCTGAGTAGC | 23072 |
rs528061285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43530759 | CCACTTCTTCCTGTC[A/G]TCCTTCTCTTCTGCT | 23072 |
rs528067612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43433118 | GGGGAGTGTCACTGG[C/T]ATCTAATGGGTAGAG | 23072 |
rs528082831 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43168188 | TGCACCTGCATTGCA[C/G]AAAGATCATGTTTAT | 23072 |
rs528088471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242887 | GCGTCCACCAGGGCG[C/T]TGGACACAGAGCAGG | 23072 |
rs528091863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203027 | TCAGCCCGCCTGCCC[A/C]CAGGTGAAATGAACA | 23072 |
rs528092816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43228192 | AACAAGTATGTTAGA[C/T]AAAATCTTGTAGGCC | 23072 |
rs528093863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43209894 | CCCGAGGTCATCTGC[C/T]GTGCCCAGTCCCACA | 23072 |
rs528093868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43340269 | TCTGTCGCCCAGGCT[A/G]GAGTACAGCAGAGCA | 23072 |
rs528097981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43440339 | GCACACATGCACTCT[C/T]ATTTCCAATCCTCCT | 23072 |
rs528100965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120302 | CCCCTTTATCAGATA[A/T]CACACCCTCAGAAAG | 23072 |
rs528114248 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150514 | TCCTGAGTAGCTGGG[-/A]ATTATAGGCACCTGC | 23072 |
rs528119779 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376847 | CTCCAGCCTGGGTGA[C/T]AGAGCAAGGACTCTG | 23072 |
rs528119815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43388081 | GCAATTGATTGCCTC[A/T]CCCTAACACAGACAG | 23072 |
rs528125541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256772 | CTAAAAGCAATATTT[C/T]CTAGAACAGAACCTG | 23072 |
rs528130633 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198881 | GAACTGGTGAAGTAG[A/G]AAGCACCCTCTCCAG | 23072 |
rs528132038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43481409 | GTAGCTGAGTACTGC[A/C]GACAGATTCACTGTC | 23072 |
rs528135437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43175069 | TGATTTCCTGATATC[C/T]TTTTCCCAACATTTT | 23072 |
rs528148710 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43237081 | AGAAGGAGGGAGGGA[C/G]GGAGGAAGCAGGGAT | 23072 |
rs528150844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43334452 | TCTAGAGTCAATATG[G/T]TACCTAAGAATATTG | 23072 |
rs528155352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380997 | TCCACATCCTTGCTA[A/G]CACTTGATATTGTCT | 23072 |
rs528157796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43467567 | CCAGAGGGGTTGATG[A/G]TGCATTTTCTCTGGC | 23072 |
rs528158632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43474776 | TAAACAAAATGTGGT[A/G]TATACCTGCAATGAA | 23072 |
rs528164635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43197413 | CCACCTTCCTGCTGC[C/T]TGTGGAGAGGCATTG | 23072 |
rs528176950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283208 | CCTTCAGTAAGGTCT[G/T]TAAGGTCAAAACTAA | 23072 |
rs528194161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43482465 | AATCCCTGCCTTAGA[A/G]AAGTTTGTATTCCAC | 23072 |
rs528194553 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43474303 | AAATACAAAAAATTA[C/G]CTGGGCATGGTGGCG | 23072 |
rs528213103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43333683 | TATGCTGAAGGACAG[C/T]AGCCATTACATCTTG | 23072 |
rs528215726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154705 | GCACAGGAAGCAGGA[A/G]TGTCTTAAGCCACAC | 23072 |
rs528220798 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43537485 | CTTCCCCACAGGCAA[C/T]TGTTTAGTTTAGGGG | 23072 |
rs528222200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162086 | TTGGATATCCACTTT[A/G]GTGAACATCAAGATC | 23072 |
rs528222935 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43436502 | GGGGCTGTTTTACAG[C/G]ATTTGGGTAGACAGT | 23072 |
rs528228538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420063 | AAATAAGGAAGAGGA[A/G]CAGGCTATGACCTAA | 23072 |
rs528240332 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149766 | TCTTCAAAATTTTTT[C/T]CAGACATATTTTATA | 23072 |
rs528247843 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43182667 | ATACAAATTTTAGGA[-/T]TTTTTTTCTATTTAT | 23072 |
rs528247944 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43285338 | GGACCCAGACATCTG[-/C]CATTGGTTAATGCTC | 23072 |
rs528250111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43368545 | CTTCTAGAACAGAAA[C/G]AAAGGGAAGGGATTC | 23072 |
rs528261683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191462 | ACCAGTGGATAGTCA[A/G]TGTCAGGCGTGGCCC | 23072 |
rs528263878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43277427 | GAAGCCATGGTTTTT[C/T]GTTTCTGTCTGTACT | 23072 |
rs528268292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43185465 | TCTGAAGTGGGGCCA[A/G]TCTTGTGGGACTGAG | 23072 |
rs528271875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43237633 | TATGTGTAAAGCAAG[A/G]TGAGCATTTACCATT | 23072 |
rs528291321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43426728 | TTTGGTAAAATGTAC[A/T]TATAACGTGTTCTGG | 23072 |
rs528298983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283933 | AGCTGCGGCTGCCTT[C/G]AGTGTCAGGAGTGGA | 23072 |
rs528303360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43190943 | ACCATTCTGTGAAAG[A/C]CAAGAATATTTTCCC | 23072 |
rs528313425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43374698 | AGAATGGCTTGAACC[C/T]GGGAGGCGGAGCTTG | 23072 |
rs528316327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43468207 | CAAGTTTTTACATAG[A/G]GTTCAAAGGAATGAC | 23072 |
rs528328660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43223562 | AGGTGGAAGTTGAAG[C/T]GAGCTGAGATTGCAC | 23072 |
rs528335909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43314323 | CTCAACCAGGGATCC[A/G]AGCTAGGGTTGTAGA | 23072 |
rs528339610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43276746 | GACGATTTATAGTAC[A/G]TACAAAATTAGCTCA | 23072 |
rs528340204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159836 | AGGTGCCCACCACCA[C/T]GCCCGGCTAATTTTT | 23072 |
rs528342842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43461823 | CTACAGGCAAAGGTG[G/T]CTTCTGAAAGGTGTC | 23072 |
rs528343147 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514965 | CATCAGGATCTAGCC[C/T]CCATTCAAAGGCAAA | 23072 |
rs528356415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43270937 | TGAAGAAAACCATAA[A/C]ATTTCACTAAAGGAC | 23072 |
rs528361129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43560221 | TAGAGAGAAATCACT[A/G]TAACCATCCTACTCA | 23072 |
rs528361492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43454847 | CTTTTCTCACTGAAA[A/C]GGCTGGATGGTTTTC | 23072 |
rs528370447 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43403649 | GATATTGTTTCCCAG[C/G/T]CTCTCACATATAATG | 23072 |
rs528374722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43410500 | TGGGGGTTGGTGGTG[A/G]AAGGAGACACACACA | 23072 |
rs528379699 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43461341 | GCTAAGTTCCATCAC[A/G]AACTGTTACAAACTC | 23072 |
rs528382243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43498273 | ACCACTGTGCTGGGT[A/G]GCACTTTCTAAACTG | 23072 |
rs528394101 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43252349 | TCTGCTGAGAGTGGA[A/T]CTCTTCATAGCTGTC | 23072 |
rs528407459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43180867 | TTAGAATCCTCTCTT[G/T]TAACTATTTTGAAAT | 23072 |
rs528416184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43230317 | GAGAATCACTTGAAC[C/T]CTGGAGGCAGAGGTT | 23072 |
rs528422914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43321109 | TCAACAGGCATCCTA[C/T]CCTCCAGTTTTGCCT | 23072 |
rs528422984 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132277 | AGATGTGTCTTTTAA[-/T]TTTATTTGTGATGAC | 23072 |
rs528431241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425380 | TCGGTAGGGTATCTT[A/G]ATAATGTCTTGGGCA | 23072 |
rs528431353 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43557287 | TCTGGGAGAGGCAGC[C/G]TTCAGCTCTTTCCTC | 23072 |
rs528431869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43223329 | AGCCCATTAAAACAT[G/T]TGTCAAGGCCAGGCG | 23072 |
rs528443118 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43537010 | GCTGAGTTGCAGAGG[C/T]TGAGACGGTAGAAGC | 23072 |
rs528452988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43372925 | CCTGTTTAGTCTACC[C/T]ATCAACCCCACAGCC | 23072 |
rs528455510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43274965 | GTCCTGAGACGGGCA[C/G]TCAGTGCAGAGGGAA | 23072 |
rs528470877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43195305 | CACTGTGTGTGAGGT[C/T]GCACAGTCTGGGAGG | 23072 |
rs528478060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522351 | AGTCCACTGAGTTCA[C/T]GTCCTGATTCCCTGC | 23072 |
rs528482414 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506926 | ACAAAAAAAATCAGC[C/T]AGGTATGGTGGCACA | 23072 |
rs528491174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146233 | TATTGACATTCTGGG[C/T]CCAATAATTCTTTTT | 23072 |
rs528502982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43250911 | AGGGCCCTGTTAGGC[C/T]GGAGGGCATATGACC | 23072 |
rs528516840 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468403 | CATGGCTGAGACAGC[A/G]AGAAAACCATGTGGA | 23072 |
rs528524854 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43324594 | ATGCAGAATCCCAGC[C/T]ATGATCCAAAGGGTT | 23072 |
rs528540015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43319421 | AAAAGAGAGAACATC[A/G]ATAGGTTGCAAAGTG | 23072 |
rs528541430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43466270 | GAAGTTATGCGAAAC[A/G]CTACTAAGGAAATGA | 23072 |
rs528543868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43366696 | CATCAATCACCATGT[A/G]TCTTCAATATTGGGG | 23072 |
rs528544937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222012 | ATGCTTAGTCTCAGA[C/T]CTACTGAATCAGAAT | 23072 |
rs528551830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43228636 | CACTCAGCTATGCTC[A/C]TTCAGGCCATAATAT | 23072 |
rs528568244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268788 | TTTGTTTGTTTGTTT[G/T]TTTAACAAGATCTTG | 23072 |
rs528569088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43550644 | AGGGTGCTGCTTCAC[A/G]GGGCCTCATCCTCCA | 23072 |
rs528578702 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155245 | CCTTATGAAGACACA[A/G]TATGCTGCTATTAAA | 23072 |
rs528585318 | in-del | -/T | 0.000332934 | 0.0128979 | intron-variant | HECW1 | GRCh38.p7 | 7:43507297 | AATTCAGACAGTAGA[-/T]TTTTTCAATCCCTTT | 23072 |
rs528604284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43418230 | TTGATTACATCTGTA[A/G]AGACCCTATTTCCAA | 23072 |
rs528604682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43466760 | CTGGATTTGGAAATG[C/T]TGTTGCCTCTTTGGG | 23072 |
rs528607036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43459399 | TATTTACTGAAAAGC[A/G]GAAAATATAAATATG | 23072 |
rs528609560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43502442 | TGGGCGGATCACTTG[A/G]GCCCAAGAGTTCGAG | 23072 |
rs528632184 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43364825 | TTTTATTTTCTGTAG[-/A]AAAATCACTGTCAAA | 23072 |
rs528633613 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43318972 | TCAAGGTGAAAGCCA[C/T]ATCCCTGTCTTAGTC | 23072 |
rs528637385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125894 | CCCATCCTGGAGAAG[A/T]GAACTCATAACTTCC | 23072 |
rs528644091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43228166 | AAATAACGCCCAGGG[A/G]AAATATTTGCAACAA | 23072 |
rs528649924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43401869 | CCATGCCCCTCTATC[C/T]TGTACCCATATAAGC | 23072 |
rs528654416 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43496862 | TTCAAGGGGCATGGA[C/G]GTGGTCCTTCAACTA | 23072 |
rs528656273 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43458436 | AACCAGGTCTCCAAA[-/T]TAAGTTTTATAGCCT | 23072 |
rs528659021 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43544759 | TTTACTAAATGAAGT[A/C]GTGAAATCATGTGGG | 23072 |
rs528670926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43173100 | TTACATATTCTGGTT[C/T]TATGTAAAATTTAAT | 23072 |
rs528671035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43422065 | AAACAAACAGTACAG[C/T]GAGCTCAGGGTGTTT | 23072 |
rs528682814 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43312752 | TGAAAGTTTCACCAT[A/T]CCCACGGATTGGTTT | 23072 |
rs528682959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43447193 | TTGTATTAAAAAGTG[C/T]ACTGACACTTTTCTT | 23072 |
rs528684747 | in-del | -/GATGGTGT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43129806 | AAGTCGCTGGTATAC[-/GATGGTGT]GATGGTGTGGTACCT | 23072 |
rs528685605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43353392 | AAAAAGGAAAACAAC[C/T]TTTGCCAACAACTTC | 23072 |
rs528689438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43215246 | AGCCCTTGCTGTGCC[C/T]GCATTAACCCTTTAG | 23072 |
rs528694645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43544238 | TGAAAGCAACATAAT[A/G]TTTAATACATAACAT | 23072 |
rs528698641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222537 | TGTACAATGCATCTT[A/T]CTGGGGTGAGATCTT | 23072 |
rs528710301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140708 | TCCCTTTTTGCGGTA[A/T]CAGCTCGGCTGCTGT | 23072 |
rs528710994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184960 | AATTCACTCACTATA[C/T]AGTACCAAGGGAGCA | 23072 |
rs528717235 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43536421 | GGGTGTGGCTAGAAT[-/G]GGGGAAAAGGCTGGG | 23072 |
rs528719183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43536707 | CCCAACACAGCCTGA[A/G]GGGTAGAGGTGAACA | 23072 |
rs528737249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529618 | CTGAAATGGAAACAC[C/T]GAGGTGACCACTTCA | 23072 |
rs528741721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43209249 | GGCAAGACCACATAC[A/G]GCACGCTGGCCCCCT | 23072 |
rs528747453 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43460791 | TGAGAGACCCTCCTC[A/G]AGTCACTGCATGACC | 23072 |
rs528758283 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43305624 | GTTGTTTGTTGTTTG[G/T]GGGGGACAGAGTCTC | 23072 |
rs528768136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126275 | CCCACCACTAGAAAA[A/C]TTCCTCTCTTTACTT | 23072 |
rs528775820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43490292 | GCTCCCATTCCCCAA[A/C]CGTAAATGCTGCCTG | 23072 |
rs528783715 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43273945 | CAATCTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 23072 |
rs528785177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43394404 | ATTTATTCTAGGTCC[C/T]ATTGCTCCATGCATA | 23072 |
rs528795103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43304822 | TACTGAGCATCATCT[A/G]TGTTCTTGCCAGGCA | 23072 |
rs528804981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43173714 | TGCAGCTCACCTCCC[A/G]CTGTGCAGCCCAGTT | 23072 |
rs528811739 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43346476 | CTGTTCCTTGTGCCA[C/T]GCAAAAGCTCTTCAG | 23072 |
rs528812413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43489333 | AGAAAAAGAGACTTA[C/T]AATTTCAATCCCAGA | 23072 |
rs528821446 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43426849 | GGAAAATATTCATTA[C/T]ATATGCTTTCTATTT | 23072 |
rs528825390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43215905 | CTGTGTCTCCAAGGA[C/T]GTATAGGGCCAGTGT | 23072 |
rs528839623 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43334508 | TTAGACACAAACAAC[A/C]CTTATCCGTTGCAGC | 23072 |
rs528852700 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43479387 | GTGGAGCTCAAGTGG[-/T]TAATGCTCACTCGCC | 23072 |
rs528863783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43524594 | ACATTAAATTACTCT[C/T]TCTTTTCATTCTCCT | 23072 |
rs528870433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43290979 | GCATATGGAGAATAC[G/T]CACAGTGGTAACATG | 23072 |
rs528872025 | snp | G/T | 9.93805e-05 | 0.00704843 | intron-variant | HECW1 | GRCh38.p7 | 7:43243949 | TCAGTGTGCTTTTCT[G/T]ATTATAAGAAACCAT | 23072 |
rs528875650 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43232020 | GAGCGAGACTCCATC[-/T]CAAAAAAAAAAAAAA | 23072 |
rs528880601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43433733 | CTCTGATGAAGAAAT[A/G]ACCTATGGAACTTTC | 23072 |
rs528895539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155545 | GAAATTTGTATTTTA[C/T]TTTGGCAAAAGAATT | 23072 |
rs528899722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523849 | CATGTGCCTGCAGGC[A/G]GTGGTGTGAGAGGAG | 23072 |
rs528902968 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43341323 | ATAAATAAATAAATA[A/T]ATAAATAAATAAATA | 23072 |
rs528904081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43333920 | GTCAAACATGGCCCA[A/G]TCCACACTGGGAATC | 23072 |
rs528923741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43321195 | TTTCCACATTTTGCT[C/G]TGACCTTTGGCTCTG | 23072 |
rs528931634 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43230407 | TCAAAAATAAATAAA[A/T]AAAAACAACCAGTGT | 23072 |
rs528937992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328667 | CAGTCCCTCAGATTA[A/C]ATAACAAAGCATGAC | 23072 |
rs528942762 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513278 | GTCCCTTAAGATCTT[C/T]ACACTCTGGGACTCT | 23072 |
rs528950681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43461445 | TGGGTCTAAAAATAT[C/T]GTTGAACCATTTTGA | 23072 |
rs528952017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114676 | ACGTTCTGACTAATT[C/T]CACACTATAATCCCA | 23072 |
rs528965299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43277524 | CATGACTGTATTCTC[C/T]GCCATGACTGGGACC | 23072 |
rs528965414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420757 | CAGAGGAGGAATATG[G/T]TTACACCGTGCACTA | 23072 |
rs528984591 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43468401 | GGCATGGCTGAGACA[A/G]CGAGAAAACCATGTG | 23072 |
rs528999721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43475432 | AATTGTTGAAAATAC[A/G]TGTGAACAATACTTA | 23072 |
rs529000349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328076 | TAATCGTAGCATTTT[C/G]GGAGGAAGTGGCGGA | 23072 |
rs529000523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159992 | CTGTATCTTTACAAA[C/T]ATAGTACATACATTA | 23072 |
rs529004278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427344 | TTTGTATAATTAAAG[C/T]CTTTGAGACATCTAA | 23072 |
rs529014894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43553593 | AGGATCCCTTGAACC[C/T]GGGAGGCAGAGGTTG | 23072 |
rs529017734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115516 | CATCCTATGCAGTAA[C/T]TGACAATGGCATGAG | 23072 |
rs529019335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43237717 | TTGGGTGACTCTGAG[A/C]CTGCTTTGCTAGATA | 23072 |
rs529022187 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43275036 | TGCTCAGCATCCATG[A/G]TGTCACTGAGTTATC | 23072 |
rs529026730 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43197418 | TTCCTGCTGCCTGTG[G/T]AGAGGCATTGATTAG | 23072 |
rs529027676 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515851 | AACTACCAAGTTAAA[A/G]TGCTCGCATATTTTG | 23072 |
rs529033238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156104 | AACTGTGATGAAAGA[C/T]CAATAATTGGAAGTT | 23072 |
rs529035082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148460 | AAGCCATTCTGCCAG[A/G]TGCTTTCCATCTAGT | 23072 |
rs529039151 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511347 | TGAGATTTTCTTCAA[C/T]GCCACTCTTTGGATG | 23072 |
rs529046499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43455571 | CTGGAGGATACCCCA[A/G]TCTTCCACAGCTGTC | 23072 |
rs529050960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43410681 | TGAGAAGACTTTAAA[C/T]TATGAATTTAGTCTT | 23072 |
rs529051887 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43338824 | GGATCATTTTCCTCT[-/A]AAAAAAAAAAAAGAG | 23072 |
rs529062429 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43504995 | GTAACATGACCAACT[C/G]CTGTCCCCCAACATC | 23072 |
rs529065306 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43493749 | ACCAAAATATTCAAA[C/T]ATCTTTTTCCTTCGG | 23072 |
rs529065933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43314387 | CTCACTCTAGTGTTG[A/T]GTATAGAAAGAGAGC | 23072 |
rs529085823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142424 | AGCATGCTGAAGGGT[A/G]GCACTGGAGACCAAG | 23072 |
rs529101405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43231482 | ACTTAGTGCCTTCAC[A/G]GAGACTCACTGCTTG | 23072 |
rs529103071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511826 | CCAGCATTTTAGCAA[A/G]GGGAAGCTAGGAGAG | 23072 |
rs529104030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43455944 | AGGTGGAGGTTGCAG[C/T]GAGCCAAGATCGCAC | 23072 |
rs529106363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43449277 | AGCCCATCTTTGGAA[C/T]AGCAGTCTGTCCACA | 23072 |
rs529106919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43186035 | GGCCTATACTACTCA[A/G]TAGGTCCTGGATAAC | 23072 |
rs529109893 | in-del | -/AAAA | 0.366266 | 0.221319 | intron-variant | HECW1 | GRCh38.p7 | 7:43319394 | GCGAGACTCCGTCTC[-/AAAA]AAAAAAAAAAAAGAG | 23072 |
rs529133768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127663 | CAGAGCAAGTCCCTA[A/G]TTCTCTCCAATTCTA | 23072 |
rs529135221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43278041 | CCCTTCCTGGTGGTC[A/G]CATCTACTCTTGTGA | 23072 |
rs529146834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369153 | ATAAATGTCACTCTT[C/T]GCTGACATAAAGAGA | 23072 |
rs529152174 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43538721 | ACCAAAACCATAAAA[C/T]AGAATTGTTGCAAGG | 23072 |
rs529160501 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43496104 | ACTTTAAATGTTTTG[C/T]TGCAATATGGGATTG | 23072 |
rs529170452 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556468 | AAGGCAGGCGGATAG[C/T]TTGCGCCCAAGAGTT | 23072 |
rs529171040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136192 | AATCAGAGGCGCCTG[A/C]TACTACTATAGACAG | 23072 |
rs529172848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43499635 | AATTAAACAAGAAAA[A/G]AAAAAAGTTAAAGAT | 23072 |
rs529180456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43404911 | AACCCGGGAGGCGGA[A/G]GTTGCAGTGAGCCAA | 23072 |
rs529185853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43547345 | CAAAGTCAAGAGATC[C/G]AGACCATCCTGGCCA | 23072 |
rs529187904 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43492253 | TTTTTTGTTTGTTTT[A/T]CTGGTTTTTGTCATG | 23072 |
rs529198243 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468122 | CACACACCAACCCTG[A/T]GTACCGTCACATTGT | 23072 |
rs529198264 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43303726 | GGCTGAAAGCACAAA[G/T]TGAGGCACAGGTTTC | 23072 |
rs529199619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43217704 | ATCACTCCTCTTCTC[G/T]TTCTGAACTGTATCC | 23072 |
rs529203662 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354632 | AAAAGAAAAAACAAT[A/T]AAAAGGAACAAAGAT | 23072 |
rs529203819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269529 | ACACTTGAAGCATAT[C/T]TGGGTTAGGAAGACA | 23072 |
rs529208448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43175543 | CAGTGCTGACCGAGT[C/T]AGGAGTTTCCCTTAC | 23072 |
rs529212569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43404209 | CCATGAAACGTATAT[C/T]TCAGTGAGTATTTAG | 23072 |
rs529230612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43551471 | ATTTTAGGAAATAAG[C/T]CATAATTGCATGTGA | 23072 |
rs529233150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142817 | TTCCGGCTTGTCTTG[C/T]ATCCACTCCTATCTG | 23072 |
rs529233988 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43365353 | TGAGGCCTGGGACTG[C/T]GGCCTCCAGATAGAA | 23072 |
rs529238622 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43179928 | TGAATGAAGGTTCAA[G/T]TTGACCAGGGATGTT | 23072 |
rs529239761 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43505760 | GCCTATTTATTCTTT[A/C]GATTGTCCCCAGAGA | 23072 |
rs529241008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43408575 | CCTGTGGTCCCAGCT[A/T]CTGGAGAGGCTGATG | 23072 |
rs529257120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43367682 | AGAGTTTTAGAATGA[A/C]CTTTTTAAGGGGTTA | 23072 |
rs529260135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509747 | CACCTGGGATGCAGG[C/T]ACTTTCCTGCTGCAT | 23072 |
rs529262769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43558984 | TGGAAGAAGATTGGC[A/T]TGAAGGGAAGACACA | 23072 |
rs529270122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43319533 | CTGACCACCCGCCCC[C/G]CACCCGCCGGCCTCC | 23072 |
rs529274142 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43484124 | GAGTATCAATCATTG[-/A]TTCATTCCTCCCCTG | 23072 |
rs529274305 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43360643 | TAGGATGGATGCTGA[A/C/G]AAGTCTAAATAATGG | 23072 |
rs529274717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147590 | TTGTATCAAAGGTAA[A/G]CAAAGAGTTTTTAAG | 23072 |
rs529284381 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510751 | GAGGAGACGGTGGCA[C/T]AGGACAACAGGGACA | 23072 |
rs529287958 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155654 | GCTGAGTGTGTACCT[C/G]TCTACTCAGTTTGTA | 23072 |
rs529295061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43275865 | CTAATTGATCCACAG[C/G]CCACCTCTGGTGATT | 23072 |
rs529296721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43190340 | GCTGGTCTTGAACTC[C/T]TGACCTCATGATCCG | 23072 |
rs529297797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140147 | CCCATTCACCTTGAA[A/T]CTTTGGAATTTTGGA | 23072 |
rs529305492 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43392555 | CAAAATTTTGGGTAA[A/G]ATGATGTTCCCAGGC | 23072 |
rs529307438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43305022 | GCTGCGGGACTGAGA[A/G]CAGTCACTGAGTTCA | 23072 |
rs529320938 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43486978 | TGAACATGATGTTTA[C/T]TGCCCGCTTCTTATT | 23072 |
rs529326490 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43313395 | CAGGCTGGAGTTCAG[C/T]GGTGCGATCTCAGCT | 23072 |
rs529333330 | snp | G/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299517 | TTCCAAGTTTAGTCC[G/T]GCATAATTGAGAAAA | 23072 |
rs529337585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43366903 | GAGATCCCGGGAGAG[C/T]AGGCAGCCTTACACA | 23072 |
rs529349237 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43180470 | GTGCGATCTCGGCTC[A/T]CTGCAAGCTCCACCC | 23072 |
rs529354952 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43303884 | CAGTTCCCAAGCAGA[G/T]GTACAAATGGGTAAG | 23072 |
rs529363637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269946 | TGGCTCAAAATGTAA[A/C]ACAAGGTTGAGAAGC | 23072 |
rs529367075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43223100 | CTTCCAGTTCACTCA[A/G]GTTAAAAAATGAAGT | 23072 |
rs529374922 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157108 | TGCATCTTTATTTCA[A/G]AGGAATTTACATTCA | 23072 |
rs529384135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43503926 | CTGTGTACATCCCAA[A/C]ACCTGGTATTCCACC | 23072 |
rs529384608 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43551976 | ATATCTAAGCACCCC[C/G]CCAAAGGCCCCACCT | 23072 |
rs529386277 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43460998 | TGCTCTGCTGTGTTT[A/G]CTGCATATTGGGAAG | 23072 |
rs529386963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43497563 | AATGTTTAGGCAGCT[C/T]TGTGGGGAAAAGATA | 23072 |
rs529388321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43401995 | GTTGAGAGGAGTTCA[A/G]TTGGGGAAGGTCGAA | 23072 |
rs529411365 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130381 | TGAAGGTAATTATAC[A/C]ATATTTTTGATAATT | 23072 |
rs529424851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43174361 | TGGGTCTCAGAGCCA[A/G]CCAGCCAACTTTGCA | 23072 |
rs529434755 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43312849 | AATCAGCTGTCATGG[A/T]AATTGATGTGTTTAC | 23072 |
rs529440226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530320 | ATTTGAAACTCTACC[A/G]TCTTAGATTCTGACA | 23072 |
rs529440724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43490346 | TCTCCTCCCTTTCTG[A/G]TTCTGGTTCTGAGTG | 23072 |
rs529445060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120349 | CACAATGTGCTCTCT[C/T]CCATCTGCTTGTTTG | 23072 |
rs529453035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43320212 | AAGTGGAGTCCGTGA[C/G]AACTAGACCCCAAAG | 23072 |
rs529459090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222596 | CTGAATTAGAGTCTA[A/C]AGATACTGTTCTTCT | 23072 |
rs529473622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43536839 | AACTCCTCCGCGAGG[C/T]CCCTCTAAGACAGCA | 23072 |
rs529484716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43274481 | TGGGCCGGCACCGCA[C/T]CCAGGCCCACTGCAT | 23072 |
rs529485816 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43173871 | TTTTTGGAGACAGGG[A/T]ATCACTCTGTTAGTC | 23072 |
rs529492298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43264315 | TTTTTTAGATTCCAC[A/G]TATAAGTGAGATCAT | 23072 |
rs529492633 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43545545 | CATAACTTTTGATTT[C/T]CCAAAAACTTAACTA | 23072 |
rs529505782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43346877 | TATACCAGTACCATG[A/C]TGTTTTGGTGACTAT | 23072 |
rs529521213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203620 | CTGCCACCATACCCG[A/G]CTAATTTTTGTATTT | 23072 |
rs529521503 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43256407 | CTGAGGTCAGGAGTT[A/C]AAGACCAGCCTGGCC | 23072 |
rs529521942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162200 | GATATTTAGAACTTA[C/G]TTGTTAGTGGATCAG | 23072 |
rs529523123 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43354167 | ATTACAAAGAATCTC[C/T]ACACAAACATATCCA | 23072 |
rs529527354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134297 | TACTTGGGAGGCTGA[A/G]GCAGAAGAACCGCTT | 23072 |
rs529529101 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180688 | GCGTGAGCCACCGCG[C/T]CTGGCCAGTTTTATT | 23072 |
rs529529312 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43464892 | CTGCAGCCTCAAACT[A/C]CTGGGCTCAAACAGT | 23072 |
rs529545955 | in-del | -/ATTC | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43475545 | TGATAAAAATTAAAT[-/ATTC]ATTTATTTATTTATT | 23072 |
rs529546769 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43267518 | AGAAAAGAAAATAAC[-/T]GTGTTCAAGTAAAAA | 23072 |
rs529554195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120805 | CACACCACCACACCC[A/G]GCTGATTTTTGTATT | 23072 |
rs529557646 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43402647 | AAGAAAACTCGAGAA[C/T]TGGGGACATTGCAAT | 23072 |
rs529566441 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | HECW1 | GRCh38.p7 | 7:43439547 | CTGGAGAACAAAAAC[A/G]GGGGCTGTGTGGGAT | 23072 |
rs529586411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43228545 | GTTTGGGGGAGAAGA[A/T]CACTTGCATGGATCA | 23072 |
rs529589247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43482608 | AAGGAAAAGTATCTT[C/T]TAAAATAAGGTGCCT | 23072 |
rs529592216 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43231791 | GGAGGCCAAGGTGGG[A/C]GGATCACGAGGTCAG | 23072 |
rs529596470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210067 | ATGGTTTTAAGTCAA[C/T]AGCCGGGGACTGGCA | 23072 |
rs529598295 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43441701 | TGCCACAGATAATAC[A/G]TAAGCTAACAAGCAT | 23072 |
rs529601839 | in-del | -/T/TTT | 0.376449 | 0.239055 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514301 | TTTTCTTTTCTTTTC[-/T/TTT]TTTTTTTTTTTTTTG | 23072 |
rs529618615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43250221 | AAAATTCTGGATAGG[A/G]ATTATGCTGGGTCAC | 23072 |
rs529632425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43254307 | ATAATGAAGCCCCAC[G/T]TAAGTGAAAATAACA | 23072 |
rs529636786 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43352047 | TCAAATATTCTTTTC[A/G]GCTTCTCAGCCTCTC | 23072 |
rs529647779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43347809 | CAATTCTGTTTATGT[A/G]GTATATCACATTTAT | 23072 |
rs529651600 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43496067 | CATCCCTATTATATA[A/T]CACATTACAACAATC | 23072 |
rs529655158 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377101 | CATTCGGACAAGTCA[C/G]AGATGCCTGGGACTG | 23072 |
rs529656855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43452739 | AAAAATAGACCAGGG[C/T]GAGGGATCTCTGAGT | 23072 |
rs529668006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43172049 | TTGGGAGGCTGAGGC[A/G]GGTGGATAACTTGAG | 23072 |
rs529670669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43445623 | ATCAGGGGGACAAAG[C/G]TGTCACCAACAGTTT | 23072 |
rs529676848 | snp | A/G | 0.000785001 | 0.0197961 | missense | HECW1 | GRCh38.p7 | 7:43311802 | GGCCTGGCCGCCATG[A/G]CGTCTCCTTCTAGAA | 23072 |
rs529680804 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43401023 | AGGACTCTGTGATTA[C/T]GTTGCACTCACCTGG | 23072 |
rs529694494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214606 | GTGGTGATCGTTACT[A/G]TGTCAGTCAGGATCC | 23072 |
rs529695883 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354352 | ATGAGACAGCAATAC[A/G]TGTACTCTCTAACAA | 23072 |
rs529706356 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248545 | TATAAATTGACAAAG[C/T]CATGAGAAGCCTCTC | 23072 |
rs529717811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43166589 | AAGTAAAAGCTTTTC[C/T]TTACTAAAAAGATGT | 23072 |
rs529718613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43489010 | TCAGAAGTAGGCACC[A/G]TTAATGAATTTCCTG | 23072 |
rs529723707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43261996 | GAAGCCAAGGCAGGA[C/G]AATCACTTGAGACCA | 23072 |
rs529744045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43255293 | ATAACTTCAGTCACC[A/G]TTGCATAAAATAAGA | 23072 |
rs529763693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43425483 | CTCTTGTTTCTTGCC[C/T]CAGCCTCCTGCGCTA | 23072 |
rs529765074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43172824 | AGCGATCCTTGGACA[C/T]AGCATGAAGGACTCG | 23072 |
rs529768647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43528891 | AATCATTTCCACATA[A/G]AGGGAAGCTATGAAA | 23072 |
rs529788375 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118917 | CTGACTCCACATCCC[C/G/T]CATGATGGATTTTCT | 23072 |
rs529788400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43386428 | AGAGCCAAGCCATCC[C/T]GACTCAGCCCAGAGT | 23072 |
rs529791306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43215123 | GGTTCTTGATTTACA[G/T]TCTTCTTGTTTACTA | 23072 |
rs529802457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43393744 | GCTTCTTTGTAAATA[C/G]TATGAATGCCAGCAG | 23072 |
rs529808329 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43168483 | GGCAACATACTGAGA[C/G]CCTATCTTCTCAAAA | 23072 |
rs529821009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43166101 | GTTTTTGGTTTTTTT[G/T]GAGACAGAGTTTCAC | 23072 |
rs529824271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43289625 | TGCCCATTGGCCTGG[A/C]CCATAGGTGGTCTTA | 23072 |
rs529835316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439172 | TAAAGAACCTAGCAC[A/G]GCCACTGGCACGTAG | 23072 |
rs529837474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207534 | AATATATTACTGTTA[A/G]TTGTAGTCATCTTAC | 23072 |
rs529864025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521771 | TCCCAGCTACTCAGG[A/G]AGGCTAAGGCAGGAG | 23072 |
rs529867190 | in-del | -/TCCC | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160893 | CTTTTACAGTTGTCG[-/TCCC]TATTTATTTATTTAC | 23072 |
rs529867285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43379203 | TCAAGCTCCCTTTAA[C/T]GCTCAATCCCAGAAG | 23072 |
rs529868410 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43373986 | TCCTCCCTTTTTAAG[A/G]CTGAATAGTATTCCC | 23072 |
rs529869939 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224416 | GGGAGCCCAGGGGGA[C/T]ACTCACAACCTAGCT | 23072 |
rs529883234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522430 | CAAGACAGTTGCCTC[C/T]TGGACTGAGTCAGAG | 23072 |
rs529886536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43473141 | TGTTAAAAACAGCCT[A/G]GCACCCACCCTCTAC | 23072 |
rs529898084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43388870 | TGCCAGTGGGTGCCT[C/T]TTGATGAGTTTGAAC | 23072 |
rs529899051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43372993 | ATCAATACTGAAACC[A/C]ATGATTTAATTAAAT | 23072 |
rs529919345 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43236314 | AGTGATTTGGGAAAC[A/C]ATTCATGGGGGGGAA | 23072 |
rs529920023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43339360 | TATCTCCCGGTTTAC[A/G]AACCCTCTTTCTGCT | 23072 |
rs529935555 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143292 | GCCTTTCTTTTTTAT[A/G]TATTGTTTTGAGACA | 23072 |
rs529970143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43466926 | TCATTTTCACTGATA[C/G]AATTTCAAAGCAGAG | 23072 |
rs529972241 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112278 | TGTGTGTAAGGTAAG[C/T]GAGGAAAGTGTCTAA | 23072 |
rs529974306 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146838 | GACAGCTCATGGCCC[A/T]TTAGTGTATGGTGCT | 23072 |
rs529991792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43200905 | GAAACCTTACCAAAG[C/T]GGCTCGATGGAAGGA | 23072 |
rs529998234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43326714 | GTGTCTTGGTGACAA[C/T]TGAGACATGAATGGC | 23072 |
rs530001474 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43227655 | AATTGACATTTTTTC[G/T]TACTTGAAATTATTA | 23072 |
rs530004515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43196444 | TGCATTCAATTGTTC[C/G]GTTTTGCATAAGTGA | 23072 |
rs530026035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520508 | CTCTCATTTACATGG[A/G]CGCAAATTTCCTACC | 23072 |
rs530026421 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43429712 | TTGCTTCTTGCCTGC[C/T]CTTTCTCCTCCAGGT | 23072 |
rs530029598 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43164924 | AGTGTCTTAAGAGTG[A/C]AGAGTCATGGCTGAA | 23072 |
rs530037603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43558334 | GAGTCATGAGCAATT[A/T]ACTGGCCTAAAAGTT | 23072 |
rs530051109 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516216 | TAGCTTTCCTAGTCA[A/C/T]ATACTTGGCGCTCAG | 23072 |
rs530052596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206798 | GGTTTCTTAAATCCA[A/G]TTCACTTCTAGATTC | 23072 |
rs530090189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43528131 | CTTGCCTGGATAACT[A/T]AATGCACATCGTTTT | 23072 |
rs530094926 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43390873 | GGCTGGAATGTAACA[A/T]AGAGCCCACCAAGAG | 23072 |
rs530104660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43324657 | CTCTTTGCAGTCTCC[C/T]GGCAGTAATAAACAC | 23072 |
rs530112869 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514923 | GAGGACCAGGTAGGA[A/G]TAGGAACCCAGGTAT | 23072 |
rs530114875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43331486 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCTGG | 23072 |
rs530116756 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562622 | ATGCAATGCATCCCA[A/G]TGGTTGTGGGGATTG | 23072 |
rs530125591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521791 | TAAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 23072 |
rs530145114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43384531 | GTTACATTAGCAAGA[A/G]AAAAATACGTCTTTG | 23072 |
rs530149423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253368 | TGACCATGGTGGTGG[G/T]GATGGCGAGGATGCA | 23072 |
rs530151185 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43246345 | TCATTTAATTGACCA[C/T]TTAATGTATTTTCAG | 23072 |
rs530152950 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43230472 | AACACAAGATCTTGC[A/G]TCTTGGATTTTTCTT | 23072 |
rs530153663 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563158 | ACCCATAGTAATCCT[A/C]CTGGGGCAGAAACAT | 23072 |
rs530157579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43478782 | AAAATATACACATTC[C/T]ATAATAAAAAAGAGC | 23072 |
rs530162332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43423399 | CACTCTTCTGTTTAC[A/G]TGGGGTGGGAGACTG | 23072 |
rs530168607 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43448610 | GGGTTCTTCCAGGCA[A/G]ACAAGCAGTGAGGGT | 23072 |
rs530169005 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110870 | CATTGCACCTGACAT[A/G]TAGAAGCTGCTCTAC | 23072 |
rs530172025 | in-del | -/CTTG | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43546657 | AAAGGTAGTCCCTTT[-/CTTG]CTGGCAAGGTACTTC | 23072 |
rs530175359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43330861 | GGTGAGTCTGCACTG[A/C]TAAAGAAGAGGCCAG | 23072 |
rs530177827 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43471930 | TAATTTTCTTTGGAA[A/G]ATAGAACTATTTAAA | 23072 |
rs530178683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43378603 | TGAGGTCGGGAGTTT[C/G]AGACCAGCCTGGCCA | 23072 |
rs530181840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117970 | AATAAGGATGTGGCA[C/T]ACAGACAGGCTCTCC | 23072 |
rs530188573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43267426 | TAATAATTATACATT[A/T]AAACTTAGCAGATGT | 23072 |
rs530201818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43280370 | TTGTGGATTTGGTCC[A/G]AATTTACTCTAGGAA | 23072 |
rs530217416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43234067 | CAGCGTGCAATATAC[A/G]GGTTGCTAAACAAGC | 23072 |
rs530219174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43226631 | TTCCAGATCCTTGAC[A/G]AAGCGGGTGCCAGGG | 23072 |
rs530220897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43479552 | CCTGTATATTACTGA[C/T]TCCATTTTGGCCTAT | 23072 |
rs530222018 | in-del | -/TTC | 0.00597842 | 0.0543458 | intron-variant | HECW1 | GRCh38.p7 | 7:43206521 | TGTGTTCTACTTCAA[-/TTC]TTTAGTGGTTAACTT | 23072 |
rs530222355 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | HECW1 | GRCh38.p7 | 7:43240293 | CAGTGAGCCGAGATC[C/G/T]GGCCACTACACTCCA | 23072 |
rs530233176 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43557047 | TGAATAGTGACCCCT[-/G]GTCCAATCTCCTTTG | 23072 |
rs530243600 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43314136 | AGTTTTGAGTCAACT[C/T]AAGGGCATCTTCCCG | 23072 |
rs530246121 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | HECW1 | GRCh38.p7 | 7:43415389 | TGTAGGGTTTCTGCC[A/G]AGAGATCCGCTGTTA | 23072 |
rs530249334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | HECW1, LOC100506895 | GRCh38.p7 | 7:43513009 | AAAAAATAAGCTCTA[C/T]TGGAGCAGAGACACT | 23072 |
rs530255489 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43479313 | ATCCCACACATGCAC[G/T]GTTCACAATGGGGTT | 23072 |
rs530276373 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43274556 | GGGCCACGCTTCACC[A/C]CCAAGAGGCCCAACA | 23072 |
rs530280576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43183726 | AACGAGTATAATTCA[A/G]ATTGAATGTTGTTTG | 23072 |
rs530280808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43364600 | GGCGCCATGAGTGGG[C/T]CTTGGCCATGCCTTG | 23072 |
rs530283018 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43505912 | TCTTCTCTAAATTGT[A/G]AGCTTAGTACCTGGA | 23072 |
rs530283494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43452214 | TACTTCCTAGGTAAC[A/G]TTTATTTGAAAAATA | 23072 |
rs530289941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43221341 | GGTCATTTTATATTT[C/T]GATCTCTTTAGGCCA | 23072 |
rs530297447 | snp | A/G | 1.69677e-05 | 0.00291266 | intron-variant | HECW1 | GRCh38.p7 | 7:43542005 | TTTGGACAGGTTTGT[A/G]TGACATGGGGTTTGG | 23072 |
rs530304022 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43380301 | ACTCCTGGGCTCAAG[C/T]GATTCTCCTGTCTTG | 23072 |
rs530304284 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350210 | ATCCCTTCTAGCTTG[C/T]AGGGTTTCTGCTGAG | 23072 |
rs530308165 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130925 | TATGTATGTATCTAT[C/T]ATGCATTGATTCTTT | 23072 |
rs530310941 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43325237 | GAACACTGACAGAAG[A/G]CAGAACTGGTGAAAT | 23072 |
rs530317519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145451 | CAGATATGTGCCACC[A/G]CGCCTGGCTAATTTT | 23072 |
rs530326413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43495504 | ACTTGTGTCTCCCTA[C/T]AGCACTCTAAGCTCT | 23072 |
rs530329845 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43503934 | ATCCCAAAACCTGGT[A/G]TTCCACCAAGACCAC | 23072 |
rs530332417 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151927 | GAAAAAGACACATAC[A/G]TATACATATCCTAAT | 23072 |
rs530349984 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43289341 | CAATCTCCTGACCTC[A/G]TGATCTGCCTGCTTT | 23072 |
rs530351258 | in-del | -/T | | | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563007 | TATTTTTTTTTCACA[-/T]TTTTTTTTCCTTTTC | 23072 |
rs530362525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43501563 | TTGCTGGGCAGGTGG[C/T]TCATGCTTATAATCC | 23072 |
rs530366017 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43321319 | CTATCATATATCTTA[C/T]TTATATGTTTTCTAA | 23072 |
rs530366641 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146043 | TCTCCACTACCCCGT[A/G]TCTCCTCTTTGGTTT | 23072 |
rs530375435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43220706 | ATCATTTTTGGCTGA[C/G]CAGGTACATTAAAGA | 23072 |
rs530375546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43227048 | ATATTCATCTAGACA[A/G]TATAATCTGGAAGTC | 23072 |
rs530396931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43270050 | GTAAGCCCTGTTACT[A/G]GAATATAGTAAGTGC | 23072 |
rs530398051 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43400377 | CTAAGGATTCCAGCA[A/G]CAACCAGTTGGACAA | 23072 |
rs530404851 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43292853 | CTGCAAGTTGTCCAG[G/T]TTCTTGGCATTTTGA | 23072 |
rs530414483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256310 | AAGCCAAGTAAAAAC[A/G]TAGTAAAGATGAACA | 23072 |
rs530420853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43178648 | CGCCCCTTGTCTTGC[A/G]TTCTCTCACATCCCT | 23072 |
rs530424169 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43339432 | TTCAGCTATTCTATT[C/T]TTCAGTAATAAAATC | 23072 |
rs530434150 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43352583 | TAAATCCTAGGTCTG[A/C]CATGAACCATATGTG | 23072 |
rs530440917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43268003 | TCACCTGATAGTTAT[C/T]ACAGACAAATATAGA | 23072 |
rs530442336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439321 | TCAATAATTATGTAA[A/C]CCCAAGGCTTGTGGG | 23072 |
rs530443830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43446939 | CTGGGCGCAGGAAGA[C/T]GGAGTGGCATCAGGT | 23072 |
rs530444254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147060 | GCAGTGGGTAATGGA[A/G]ATTTTGTACTTTTAA | 23072 |
rs530445857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125626 | AGCCGGGCATGGTGT[C/G]ACATGGCTGTAATCC | 23072 |
rs530454305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508835 | TGCCATTGGCATTCA[C/T]TCCAAAGAGCAGAGG | 23072 |
rs530471882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43318048 | GACTTGTTCACCAGT[A/G]TATCCCCAGGGTTTA | 23072 |
rs530479942 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117951 | TGCATATGGAGGCCT[A/G]AAAAATAAGGATGTG | 23072 |
rs530480100 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43417182 | CAACCTCCCGAGTAG[C/G]TGGGATTACAGGCAC | 23072 |
rs530480180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161599 | AAAGATATTTCAAAT[A/G]TCGCTTTCAGATAAT | 23072 |
rs530489532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242751 | AGGCAGTGCAGGGGA[C/G]CCTGCAGATGGGGCA | 23072 |
rs530508129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43481265 | CAAAGTACAAGGTGG[G/T]TTGTCTTGAGATTAT | 23072 |
rs530509021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529581 | CAAAATCACGTCCAC[C/T]GTGAGATGACTTCAG | 23072 |
rs530518572 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43224727 | AGCTGAAGTGAGAGG[A/T]TCACCTGAGCCCAGG | 23072 |
rs530519859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43202993 | CCCCTATCTCCCTTC[A/G]CTGATTCTCTTTTTG | 23072 |
rs530524292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43242269 | TGCAGACGAGGAGGC[C/T]GGTTAGGCTCCATGG | 23072 |
rs530531729 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43113006 | CTCTGGGCGGCTTCC[C/G]CGCCGCACGCGAGGC | 23072 |
rs530544997 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133618 | TTTTATATTTCTCTC[-/TT]TCTTTCTCTGTTCCT | 23072 |
rs530552547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43394321 | CATTGATGGGAATAA[C/T]AGACATAAAGGAGGA | 23072 |
rs530563193 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122714 | AGGAAAGGAAAAAAA[-/T]ATCACTATATGTATA | 23072 |
rs530579809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43333589 | ATTTCCCCTTAGAAG[G/T]CTTAATAAGTATGTA | 23072 |
rs530598665 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43236332 | TCATGGGGGGGAAAA[C/G]CTCAAATGAAATAGT | 23072 |
rs530610014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43289667 | ACAGAACTCTGTAAA[A/G]TATTTAAAGAGGTTT | 23072 |
rs530613920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154614 | GTGTATATTAGGAAA[C/T]ATTAGTATGCATTTG | 23072 |
rs530635544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516268 | AAGGAAAAAAAGAAA[A/G]GAGGGAGGGAAGAAG | 23072 |
rs530639564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43432909 | ATAATAAGCATCTTA[G/T]TTCTATAAATGGCCT | 23072 |
rs530639790 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440308 | GCCCTGAGATATTTG[C/T]ACCTTTCCCCCCTGG | 23072 |
rs530641442 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43402024 | AAGAGGAGATTGGCC[A/G]AGGGACAGCCAAACT | 23072 |
rs530641541 | in-del | -/ACTC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198427 | CTCTCTTACACTCAT[-/ACTC]ACATTCACACACTCA | 23072 |
rs530649302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43289042 | AGTGCCTGGCTGGTA[C/T]TAGGCATTTCCCAAT | 23072 |
rs530651017 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43374570 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCCGGCT | 23072 |
rs530661416 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43380384 | GAGTTTCTTTTGCTC[A/G]ACATTACTTTTGTAG | 23072 |
rs530663128 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43354978 | GCAGACTTCTTAATG[A/G]AAACCATAGAGACCA | 23072 |
rs530666672 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43467027 | ATATGATTTTACATA[C/T]GTAGTTTTTTCATTG | 23072 |
rs530677866 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43380298 | CAAACTCCTGGGCTC[A/C]AGCGATTCTCCTGTC | 23072 |
rs530683478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43418344 | CTAATTTAATCTATT[C/G]TTGGTTCACTGAACT | 23072 |
rs530683634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43426133 | TTGACCAATCATGGG[A/G]CACTTAATGACCTGA | 23072 |
rs530687545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43283156 | AAGAAAGAAATTCTC[A/G]GTGTACAGTTTGGGG | 23072 |
rs530688436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140821 | CCACTGAGTCCGTTC[C/T]TGGTGAGGGCTTGCT | 23072 |
rs530688875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43352750 | ATTGGCTATACATCA[C/T]AGGATTCTTGTGAGG | 23072 |
rs530692683 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43276673 | TTAGGCCAATGCAGT[A/C]TTCCCTGTCCACTGG | 23072 |
rs530738458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523137 | GCCTCTCAAGTAGCT[A/G]GGATTACAGGTGTGT | 23072 |
rs530740816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43559612 | GGAAGATTAATTGAC[C/T]TTTCCAGTGTCATAA | 23072 |
rs530747321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147683 | GTGATGATTCATCTT[C/G]CATCTCCCAACTAGG | 23072 |
rs530754119 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468061 | CTGGCCCAACCCCCC[A/G]TCTACACGTGGTCTG | 23072 |
rs530757619 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43236990 | AATAGTAAATGAAAC[A/C]AAAAAAAAACTAACT | 23072 |
rs530757733 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43285249 | CTGGATCAGGGTCTC[-/A]ACCTGTGGAGCTCTG | 23072 |
rs530758608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43332941 | ATTCAACCGGTCCCA[C/T]AGTCACAGGTAACAA | 23072 |
rs530763177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43196562 | CTCAGAGGGTAACTG[C/T]ATATGCATGAATCTC | 23072 |
rs530772606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424264 | GACAGGCTTTGCTCC[A/G]TGTAGCTTTCTCAGC | 23072 |
rs530789223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222661 | GCTAACACCGGAGTT[G/T]CAAATTATTCAATTA | 23072 |
rs530789980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43320312 | GATTTTCACACTGAG[C/T]TTTCACACATAGAAA | 23072 |
rs530792565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514460 | CGCCCAGCTAATTTT[C/T]GTATTTTTAGTAGAG | 23072 |
rs530795071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521573 | AACCCCCAAGGTGAT[C/G]GTATTAAGAAGTCAG | 23072 |
rs530804331 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43506963 | TGATCCCAGCTACTC[A/G]GGAGGCTGAAGTAGC | 23072 |
rs530806516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159975 | TGAGCCACCGCGCCC[A/G]GCTGTATCTTTACAA | 23072 |
rs530811862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43280421 | AGGGCGATTAAAATG[C/T]CGAGTCACACAGCTA | 23072 |
rs530814174 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43554279 | CCTTCTACTCCTTAT[C/G]TACACCTATATGAGG | 23072 |
rs530822457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43559162 | TGGAAAAATAGAGGA[A/G]ACGGGGAGATCAACT | 23072 |
rs530827228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521121 | TAAGAGTGCCTGATG[C/T]GGTTTGACGGATGCG | 23072 |
rs530827649 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43319773 | CCTGGCTAATTTTTG[A/T]AATTTTTTTTTTTTT | 23072 |
rs530833966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43190892 | CTGCATGACTTCATA[C/T]CAAATCCCAAACTGG | 23072 |
rs530841461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43185082 | TGAAATTTGTGTGGG[A/G]ATGCAGATGCAAACC | 23072 |
rs530846063 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43201572 | ATCTTTACATTCCCC[A/G]TGGTAGATTTGTGAC | 23072 |
rs530849119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43194525 | ATAAGCCTGTGTGTG[A/T]GCTCCCTGGACCCTT | 23072 |
rs530852859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43552097 | CAAGTTAAAAATGAT[C/T]ACAGACTCAAAAAAA | 23072 |
rs530871183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43419096 | GAGCTTCTATACATC[A/G]TTTGGGGCTCTCCTT | 23072 |
rs530873519 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43527059 | TATCCAGGCAAGCAG[C/G]CTTTTATGGTCAAAT | 23072 |
rs530873700 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43173625 | GTTCACAGTGGGGTT[C/G]ACCCTCCTATGAGAG | 23072 |
rs530875925 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157318 | AACATCCAAAAAAAT[A/G]TTATCAGTAGATTCA | 23072 |
rs530880482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43458825 | AAATTTACAATGATT[A/G]CTGGCTCACAGCCAT | 23072 |
rs530881052 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487364 | AAATGTTTGAAGTTT[G/T]CACATTTACAATTAT | 23072 |
rs530899169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43417256 | GGTTTCACCATGTTG[G/T]CCAGGCTTGTCTCAA | 23072 |
rs530906664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43371578 | TACACTATTGGGCCC[A/G]TTTTTTTCAAGGCAG | 23072 |
rs530914975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43325629 | CGCCCTTGTGTTGTC[A/G]TCACTGTCGTAGGCA | 23072 |
rs530918621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43465386 | GCTGCGGAGTCGGCC[A/T]CAGGCTGACCTGAGA | 23072 |
rs530921900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152401 | TAATAATAAGAGGCA[C/T]AAATTAATAAAATCG | 23072 |
rs530930726 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43347170 | TCTGTGATTTCTTTC[A/T]GTAGTGTTTTGCACT | 23072 |
rs530944405 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43504189 | CTTCAACATCGACAG[C/G]GACCCTCATTCCGTT | 23072 |
rs530949139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508450 | TTTCTCTTAAAGTGC[A/G]TGTATACAACTTCAT | 23072 |
rs530952906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43416849 | CTCCCTGGCCCCTTG[C/T]GCTTCCCAGGTGAGG | 23072 |
rs530959659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424728 | TGATATTGTAAATTA[A/C]TTTAAATTGCAATTT | 23072 |
rs530960006 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190167 | CGCCCAGGCTGGAGT[G/T]CAGTGGCATGATCTC | 23072 |
rs530960533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118825 | GGGCATAGGACCTGC[A/G]TATAAAGAGGATGAT | 23072 |
rs530970597 | snp | A/G | 4.79145e-05 | 0.00489438 | intron-variant | HECW1 | GRCh38.p7 | 7:43550615 | CGGTGGCCTGGGGAA[A/G]GCAAGCTGTGGCCAG | 23072 |
rs530974907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43472018 | TAAGAGGAAAAAGCC[A/G]CAAACAGAAAACAAG | 23072 |
rs530977448 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43378695 | CCTGTAATCCCAGCT[A/T]CTCAGGAGGCTGAGG | 23072 |
rs530983231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43372034 | ACCATGTTGGCCAGT[C/G]TGGTCTTGAACTCCT | 23072 |
rs530994240 | in-del | -/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152445 | TAAAGTTTCAAATGG[-/T]TTTTTTAAAATATGT | 23072 |
rs530995518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146206 | GGATTTAGGGTTTCT[C/T]CACCTTGGCACTATT | 23072 |
rs531003067 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111491 | AGGAAAGGACTGGGC[A/C]CCCCAAGTGGAATAC | 23072 |
rs531019467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563730 | AAAAATTAGCCGGGC[A/G]TGATGGCACATGCCG | 23072 |
rs531025118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43221533 | TAAATGTCAGAGGAA[C/T]TAGGTTTTTTTTTTT | 23072 |
rs531026440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43228113 | CACATAAAATTGGAA[A/G]TCTTCCATTAACAGC | 23072 |
rs531028272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43472660 | AAATTATTAAGGTGA[A/G]CAGATTAATTGGGCT | 23072 |
rs531058853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145499 | ACAGGGTTTTGCTAT[C/G]TTGCCCAGATTGGTT | 23072 |
rs531061224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43274936 | AAACTATACAACTCA[A/G]TGCTGTTGAAGATGT | 23072 |
rs531064079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43446294 | ACGTATTCTGTGTTT[C/T]AACCAAAGATGTTCT | 23072 |
rs531077127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268525 | TAGTGGGCAGAGGCC[A/G]GGGATGCAGCTGCAC | 23072 |
rs531088227 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123801 | CCTTCCAACCGGGTG[G/T]GCTGTGGGCTGGGAG | 23072 |
rs531091527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43502398 | ACAATGGCTAACCCG[C/G]GTAATCCCAGCACTT | 23072 |
rs531094045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132229 | TTAAGTCTATATATT[A/G]TAGATGTTAACTATC | 23072 |
rs531094460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43215180 | TTAATTACCAGTGAC[A/T]GTATAGGCACCGCCT | 23072 |
rs531108364 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43488486 | AGAAAGAAAGAAAGA[A/G]AGAGAAAGAAAGAAA | 23072 |
rs531113980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43401235 | ATCACAGAATTAAAA[A/G]CCTTCAAAAGCAGTA | 23072 |
rs531116073 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43179798 | ATACCTCAGTGTTAT[A/T]TAAAAGAGCCTAAGG | 23072 |
rs531117388 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359530 | CTGTATAATAAGTAA[G/T]GTTGTTTGAGGAGTT | 23072 |
rs531122359 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43457366 | AAAAGTTGAGAAAGA[C/T]GAAAAAGAATGAAGA | 23072 |
rs531140313 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43443794 | CCACCCTGCAGGACC[-/T]AAGCATAGGAAACAT | 23072 |
rs531160508 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43266422 | CTCACTGCGTCCTCC[C/G]CCTCCCGGGTTCAAG | 23072 |
rs531163821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43459280 | TCTGCTCCCAGCACC[C/T]AGTGTGGTACCAGAA | 23072 |
rs531164376 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43344535 | TTTTTTTCTCTGATG[A/T]CTGATTGCTTTGTTC | 23072 |
rs531165087 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43314734 | TTTCAACGGCATAGC[A/G]TTTCAAAAATAACTT | 23072 |
rs531178235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405543 | AAATGCTGTCTACCA[A/G]GGAAGCTTCTTAGAG | 23072 |
rs531181239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43184174 | GCCCACCACCATGCC[C/T]GGCTAATTTTTTGTA | 23072 |
rs531190708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43357784 | TAGCACAAAAAAAGA[A/C]AAATAATTAAGATGA | 23072 |
rs531198430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43544135 | GCTGATACAGATATC[G/T]CACAAATTCTCAAAG | 23072 |
rs531215996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136955 | TATGCCCAAAGCCAA[C/T]AGTATGACTTTTCCT | 23072 |
rs531217540 | in-del | -/TATTTATT | 0.000827814 | 0.0203279 | intron-variant | HECW1 | GRCh38.p7 | 7:43475545 | TTGATAAAAATTAAA[-/TATTTATT]TATTTATTTATTTAG | 23072 |
rs531220629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43496695 | TCAGGGAGTCATGGA[A/G]TCTCTGTCTTGGGTC | 23072 |
rs531228056 | in-del | -/TTG/TTTTTG | 0.181022 | 0.240296 | intron-variant | HECW1 | GRCh38.p7 | 7:43401575 | AAAAAGGTTTTTTTT[-/TTG/TTTTTG]TTTTTTTTTTTCCCC | 23072 |
rs531236742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43182159 | GTTTTCATTTGATAT[A/G]TTTCCACTTGTCTAT | 23072 |
rs531254905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43363996 | GGGGAAATGCTGTGA[A/G]GTTTCCCTCTATCAA | 23072 |
rs531268787 | in-del | -/C/TT | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43373220 | TTTTTTTTTTTTTTT[-/C/TT]TCTTTTTGAGACAGA | 23072 |
rs531281581 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43435053 | CATATTATTGTGATC[A/C]TGAATTGTATTTGTC | 23072 |
rs531282454 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43527234 | GACAAGCAAGGAGGA[C/G]GGCTATGCTGCGGGT | 23072 |
rs531286519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131527 | AGTGTATACAAATCA[C/T]TGACTGCATTTTTTT | 23072 |
rs531291922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43555546 | TTGCTAATAGGATAC[A/G]TTCGAATTATAAAGA | 23072 |
rs531295362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43494529 | TTTTTTTTGAGACAG[A/T]GTCTTGCTCTGTTGC | 23072 |
rs531301954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43399436 | TAACAATGATTAATA[C/T]CAACCTTCAAAAACA | 23072 |
rs531316469 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43449964 | ATTATAAGTCCGAAC[G/T]GAGAACAGTATAAGC | 23072 |
rs531316819 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142741 | TACACATTGGTTCTT[C/T]TAGCACTCCAGTTTC | 23072 |
rs531316849 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43170549 | GTAAGGTTACAGCTC[A/G]TGAACAGACCCGGAA | 23072 |
rs531317474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43364400 | TGATGGATGTGCTTA[C/T]AGAGATAAATGAAAT | 23072 |
rs531319482 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43262814 | ATCCTTGTCCATTTG[-/C]CACTTCCACCTTCTC | 23072 |
rs531320313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43267147 | ACAATTAAAACTTGT[A/G]CTGACCATTTTGCCA | 23072 |
rs531330169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43500849 | CCTCCATCACGGCCA[C/T]CCTGAAAATGGCCTA | 23072 |
rs531338893 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513692 | TTTTGGTTTTTTTTT[G/T]TTTTTTGCTTTTGGT | 23072 |
rs531353449 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43225730 | ATAGAAAATGCTGCT[A/G]ATTTTCTATGAGATC | 23072 |
rs531363390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43456860 | ACAGTTCTCAAAAGG[A/G]TAGAGACCTCAGTTA | 23072 |
rs531366785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43486552 | ATGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 23072 |
rs531387452 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43164724 | AATGGAGAAAGAGGC[G/T]AGGACAGAGAGCGCC | 23072 |
rs531389994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43527518 | TATCTCTTATAAGAA[C/T]GCTTGTCGATGGATT | 23072 |
rs531390468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43451143 | CCATGTGATCTTGAA[A/G]AGATAACACAGTGTT | 23072 |
rs531390687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43310027 | TAAATTGTCCAGTGA[C/T]AGACCCACAGCTGGG | 23072 |
rs531404836 | snp | G/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146533 | AAAAGGGGAGAAAGG[G/T]AATGGAACATTTACA | 23072 |
rs531413724 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43264738 | AGTCTCAGTTACTCC[A/G]GTGGCTGAGGCAGGA | 23072 |
rs531416531 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524298 | ATCTACCCCAGGCAG[A/G]CACAACAGGTTTTCA | 23072 |
rs531417371 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43289295 | TATTTTTAGTAAAGA[C/T]GGGGTTTCACCATGT | 23072 |
rs531417879 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119611 | CAGAACTCCAGACTT[A/G]AAAATGCAACCGCCC | 23072 |
rs531419240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213093 | ATCTATGTATTTCTC[A/G]GTGAAAGAATAGCAG | 23072 |
rs531422132 | snp | C/T | 1.68185e-05 | 0.00289982 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43444781 | AGCAGGCCCTGCTCC[C/T]TGCCTGTGTCCGAGC | 23072 |
rs531423142 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43220545 | TCATAAGCTAACTAG[C/G]AGCCCACCAGCTCTA | 23072 |
rs531428167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130683 | GTATCAGCTGTTAGA[C/T]AATGACAACAAACAT | 23072 |
rs531428306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206402 | GTCTACCGTGCTTTT[A/T]TCTGGTCTTTTATTT | 23072 |
rs531436247 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43422488 | CTACCTCAGCCTCCC[C/G]AGTAGCTGAGATTAC | 23072 |
rs531444605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43170533 | GAAGGGGTTAGTCAC[C/T]GTAAGGTTACAGCTC | 23072 |
rs531466273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43165861 | ACCATGCCATCAGCC[A/G]TTTGCATGTGTTGAG | 23072 |
rs531477631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43317235 | ACACCAACAGGCAGT[C/G]GGGGTGGGGGCAGGC | 23072 |
rs531485185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43495235 | CGTCATCTACATTAG[G/T]TATTTCTCCTAATGC | 23072 |
rs531490654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124143 | ACTAAACGATGTAAT[C/G]GACGCACTATTTTTA | 23072 |
rs531491797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43295528 | TACGGAGAAGGTCCC[A/C]CTCCCCAGGGGGGCC | 23072 |
rs531493426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43287243 | GGGGATTAGGGAGGA[C/G]TAGATGAGCAGGTAC | 23072 |
rs531495698 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43552692 | TCGTGTCTGGCTTCT[C/T]TGACTTAGCCTACTG | 23072 |
rs531502488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116596 | AGACTAACAGGTGTG[A/G]CTTACAGACATCAAG | 23072 |
rs531505335 | snp | A/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214142 | TATGTATTTCTATAG[A/T]TTTTCTAGTTTTTCA | 23072 |
rs531520925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253641 | TTTGACATTCCCTCC[A/G]ATGTTAAGAGATGTG | 23072 |
rs531521939 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43392655 | TGTCTTGGGAGGCTG[A/G]AAGACCTGGGATATA | 23072 |
rs531526845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43294664 | TTGAACCTGCTGACA[C/T]TGGGAGAGCCTAGTC | 23072 |
rs531534004 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43344517 | ATGTTGTTTTTGTCT[C/T]TTTTTTTTTCTCTGA | 23072 |
rs531540465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118463 | AATTAAACATATAAG[A/G]CCTTGCCATCAGTGC | 23072 |
rs531542305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43337775 | AAACCTACAGACATT[A/T]TAGTTTCATGAAATC | 23072 |
rs531542788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43241351 | GTTCTCTTTGGTGGG[A/G]TGGGGTAAGCTTCCA | 23072 |
rs531549746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118054 | AACTTAAGCCGGTAC[C/G]AGGGGGGCGGGGGAA | 23072 |
rs531550807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302371 | CAGGCTTCAGCTTCC[C/T]GGTGAATAAGAGGAG | 23072 |
rs531554475 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43350721 | CTGAATTGTTTATTG[G/T]TTTTTTCTTTAAGCT | 23072 |
rs531555779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122239 | GTCAGAAGTAGAGCC[C/T]AGTTTTCTGCAGCGT | 23072 |
rs531557473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43493021 | AGCAGCCATTTTCCA[A/G]TCATCAGAGTGATTA | 23072 |
rs531560618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213582 | TCCTGAGTAGCTGGG[A/G]CTACAGGCGCCCGCC | 23072 |
rs531567298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43205181 | CTTCACCTCTTGGGT[A/T]CAAGAGATTCTCTTG | 23072 |
rs531585419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43443089 | CACAGAAAAACAAGA[A/G]AAGTATAAATAGGAC | 23072 |
rs531591712 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43169590 | GGCTTAATCATCATA[C/T]GCTAGTACTTTGCTC | 23072 |
rs531592059 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43349401 | TAGTTTAAGTCCATT[G/T]TTTCTTTGTTGACTT | 23072 |
rs531593481 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43316320 | GACAAAATCTTGAAC[A/G]GTACTGATGTGAGCT | 23072 |
rs531595934 | in-del | -/TGTT | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160185 | ATTTTTCTATGGGTC[-/TGTT]TGTCATTTGTTTTAT | 23072 |
rs531609925 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43348963 | AAAGTTCCATGCACT[A/C/G]TTGAATAGAATGTGT | 23072 |
rs531614423 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247534 | CAGTCACAGTTACTC[C/T]GGTGGTTGAGGCAGA | 23072 |
rs531615439 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147452 | TGTTATTGCAGAACA[A/G]ATGAAATGAAACCAT | 23072 |
rs531623127 | snp | G/T | 1.65616e-05 | 0.00287759 | missense | HECW1 | GRCh38.p7 | 7:43479635 | TGGACCACAACAGTC[G/T]AGCTACCACTTTCAT | 23072 |
rs531631725 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43244080 | GGACATTTGAGATCC[A/G]TCACCCTCCCTCCCC | 23072 |
rs531632137 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43211366 | ACACATCACCTTTCT[C/T]CTCCGTGAATGAATG | 23072 |
rs531632428 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43201140 | CTGGACTCAAATCCA[A/T]CACACACTGGTCCTT | 23072 |
rs531638040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43539709 | TGCTGACCTTTAGTC[G/T]TTTCCTGGTTTGGAT | 23072 |
rs531639593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43247122 | AAAGACTAGAAAATC[A/C]GTTCCTCTGGGCTGT | 23072 |
rs531648301 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43334247 | CTCTCAGGACTTTCT[A/G]ACATCAGTCAAGATA | 23072 |
rs531648740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530003 | CACCCATGCTGGAGT[A/G]CAGTGGTGCAATCTC | 23072 |
rs531648983 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43221710 | AGGTGCCCACCACCA[A/C/T]GCCCGGCTAATTTTT | 23072 |
rs531654721 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43421006 | CTTGAAAAAGAAAAG[A/G]AAAAAAAAGCAGGAC | 23072 |
rs531659470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43486995 | GCCCGCTTCTTATTA[C/T]AAAAATATTGAACAA | 23072 |
rs531662798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43478845 | AATTATTAATTACTA[A/G]TATTATCTTAACCCA | 23072 |
rs531672581 | snp | A/G/T | 3.3892e-05 | 0.00411641 | intron-variant | HECW1 | GRCh38.p7 | 7:43438198 | CCACCAACAGGTCGT[A/G/T]CCCAAAGGTGGCCTG | 23072 |
rs531673297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43345038 | GTGGCCATTCCACAG[A/G]CTGTGAAGTATAGAC | 23072 |
rs531686733 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43237839 | CCAGTCTTTCCCCCC[C/T]GCCGCCCCCACTTGG | 23072 |
rs531692377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43244748 | GGCCCTGTGCTGCTC[A/G]GGTAATACTCAGCCA | 23072 |
rs531701611 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43284024 | GTAGAGATGTGGGGA[G/T]TGAGTCAGGGGCCTG | 23072 |
rs531705015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43397595 | ATTTTTTGTGGGCAG[C/T]GGGTGGATCTCACCA | 23072 |
rs531720322 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43307798 | TGCTCACCACAAACC[-/A]AAACAAAATAAAATA | 23072 |
rs531729641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43532318 | CTCCCATCTGGATGC[A/G]GAAGCCTCCAGACAG | 23072 |
rs531732482 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163442 | CGGGGGGAGGTGCTG[C/T]GAAGACTGGGGAGAT | 23072 |
rs531732843 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43502170 | CTGAATCGATTGCAC[A/G]CCACTTTTGGTGATA | 23072 |
rs531733998 | snp | A/C | | | missense | HECW1 | GRCh38.p7 | 7:43444355 | AGCTGGAAGCCAGAG[A/C]AGCTGGGTGAGGGCA | 23072 |
rs531748850 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43206666 | CATACTGGGTGCTGG[A/G]TGCTGCTTTTATTTC | 23072 |
rs531763127 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43389834 | GAAAGAGTCTCACAA[C/T]GTTGCTCAGGCTGAT | 23072 |
rs531794884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43525808 | AATGGATCCTCCAGC[C/T]TAGGCTGAGAGCAGA | 23072 |
rs531806637 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110734 | GCCTGGGAGGCGGAG[A/G]TTGCAGTGAATGGAG | 23072 |
rs531807588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43205637 | CAGTAAGAATGTCGC[A/G]CAGGTTGTACACTCC | 23072 |
rs531823251 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43285934 | TACTGAAAGTACTAG[C/G]AATCCAAGTTTTGGC | 23072 |
rs531826058 | in-del | -/AA | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43354583 | AGAATCAGTGAGCTC[-/AA]AGAGAGGCTATTTGA | 23072 |
rs531831782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43336314 | GGGACCACACTCACA[C/T]ACCACCATGCCCAGC | 23072 |
rs531866057 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514304 | TCTTTTCTTTTCTTT[-/C]TTTTTTTTTTTGAGA | 23072 |
rs531870772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43272336 | AAGTTGACAAGTGGA[A/T]CCTATTAAACTAAAG | 23072 |
rs531875446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43463573 | AAGACAATTCTTTAC[A/G]GATTTCTCCAATTAT | 23072 |
rs531876358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300094 | TTCTATCAATGTTGA[A/G]AGCTTGACGGAGGTG | 23072 |
rs531880810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143684 | TGCAGCTGCTGCTTC[A/G]ACTGCCCAAAGGACT | 23072 |
rs531882107 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43543909 | TCTTTCACATATGCC[C/G]TATTGTAGAGGGTAA | 23072 |
rs531888625 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43295089 | CTGAATACACAATTT[A/G]CAGGAATAGTCACTT | 23072 |
rs531897181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43561722 | CTGCTCACTTTTGAT[C/T]CCTTTTTGAATCACA | 23072 |
rs531900451 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43428799 | ATGATCACACAGCAG[A/T]TTTTGTTCTTAGCTT | 23072 |
rs531902450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43421797 | ATGATGGCTGCTGGT[A/G]AGGTGTGGAACATAG | 23072 |
rs531903294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43187629 | GTGATTGAATTTGGG[C/G]TTTTCCTTTATATTA | 23072 |
rs531906041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286503 | AGTAAATTTAATGCC[A/G]GTTTCATTATAGTAA | 23072 |
rs531918388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150654 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG | 23072 |
rs531920360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43239982 | ATATTGTTTGTCGTC[C/T]GTATGGCTTGGCTTT | 23072 |
rs531924805 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43260913 | CCTATTGTGTGCCAA[A/G]CACTATTCTAAGAAA | 23072 |
rs531931224 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157557 | AAGGATAAAATTGAT[A/G]TATTCTTTTCTTTCT | 23072 |
rs531946895 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43320423 | TCTCCTGCCAGCAGT[A/G]CTATGGGGTTGGGAG | 23072 |
rs531951285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513305 | CTCTGCTCTCCACGA[C/T]GCGTGAATGCTGCTT | 23072 |
rs531951817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519553 | CTGGCCTAGTGCAGA[A/C]TTTTAAAAGCTATGC | 23072 |
rs531955953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43436240 | GTATTTATTTCAGGT[A/G]TTTCACAGCCCTTGA | 23072 |
rs531961059 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328519 | ACACGGCCAATGAGA[C/G]AATGGCGTGTGGCAG | 23072 |
rs531973686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359068 | TGACCACAAATGATC[C/T]ACCCACCTCGGCCTC | 23072 |
rs531977797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43399465 | CAGTAGAAACCAGGA[A/G]TACTGCACAACTATG | 23072 |
rs531985629 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43292414 | AAGGCCCCTGGAAAC[C/T]AGCCTTGATAACAAG | 23072 |
rs531985810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43364947 | TTCTTTCTCTGATTA[C/T]ACATCAAAAAACAGA | 23072 |
rs531994898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138199 | TTTTCTCAGTGATTG[A/G]AATTGCTGCTGCCCG | 23072 |
rs531998715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43322195 | CTGACTCAGCCTCCC[A/G]CGTAGCTGGGATTAC | 23072 |
rs532030890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43165229 | TTATTGAAATGTGTC[A/G]ATTTCCCTTTTTCTT | 23072 |
rs532055857 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562518 | ACATGTGGCATCAGT[C/T]CCATCAGCCGGAACT | 23072 |
rs532068167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43171938 | TCAAGCAGATAAAAG[A/G]TTTTTACAGTTGCTC | 23072 |
rs532070152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43534382 | TTACATACTAATTCC[C/T]GCTAAAACATGTTCC | 23072 |
rs532071023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43495992 | TAGAAAAGGTTTTTT[C/T]TTAAGTAATTCCCTA | 23072 |
rs532072850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43487310 | CAGTTGCTGAAAACT[A/G]TTTTCTGAGGATATC | 23072 |
rs532075339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43392884 | AAGAGCTGATCTTCA[C/T]ACTCTTTTGCTGAAT | 23072 |
rs532092782 | snp | A/G | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521174 | AACTTAATCACCAAC[A/G]TGATGATATTAAGAG | 23072 |
rs532093239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43422629 | CTGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 23072 |
rs532096721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253785 | TTGTGGCAGGTGCCT[A/G]TAATCCCAGCTACTG | 23072 |
rs532108243 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115635 | CTAAATAGGCAGGCA[A/G]GCAGTGTTTTCATGC | 23072 |
rs532116590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43406875 | AGTGAGCCAAGATCC[C/T]ACCACTGCACTTCAG | 23072 |
rs532117096 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43454789 | CTGAATGATAAGTTT[G/T]CAATGAAACTGTTAG | 23072 |
rs532118261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43178455 | CCAGGAATTTACTGG[A/G]TTAAATAAGCCACCA | 23072 |
rs532128343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43452071 | TTAAAGAAACACAAT[A/G]TTTGTTTTTCAAGGG | 23072 |
rs532138296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508246 | GTCTTCACCCCAATG[C/T]GATTCTGATCACATT | 23072 |
rs532143087 | snp | A/G | 3.39755e-05 | 0.00412148 | missense | HECW1 | GRCh38.p7 | 7:43444842 | ACCCCGAGACCCCGC[A/G]GACACACTACATCCG | 23072 |
rs532143452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302603 | TCCTCACAAATGCCC[A/G]GTACGGGGCCGCCCC | 23072 |
rs532152773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43220620 | TCATCCAAGAAATTC[C/T]AAGGATTTAGAGGCT | 23072 |
rs532158081 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43345839 | ACACATCATATATAT[A/G]TACACACACATCATA | 23072 |
rs532162524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521216 | AAGAAGTGATTAAAC[A/G]ATGAGGGCAGAGTCA | 23072 |
rs532164983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43458393 | GTGATCTGCTTGCAT[A/G]ATATAAAAATTAGGC | 23072 |
rs532165919 | snp | A/C/G | 9.95857e-05 | 0.00705578 | intron-variant | HECW1 | GRCh38.p7 | 7:43479759 | GGTAACCCTCCCTAC[A/C/G]CCCCGCCCTACTGTT | 23072 |
rs532166495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43165968 | TCAATTATTCAACCA[G/T]TGTCTATGAGCTCCT | 23072 |
rs532167737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43310146 | CTTAAAGTATGTGGG[A/G]ACTAAACAAACCTTG | 23072 |
rs532185685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303110 | CCCACAGCCCCCTGC[C/G]CATTCCTCTGCCCAT | 23072 |
rs532191652 | in-del | -/AAAATAAAAT | 0.00581995 | 0.0536293 | intron-variant | HECW1 | GRCh38.p7 | 7:43285793 | ACCCCATCTCAACAA[-/AAAATAAAAT]AAAATAAAATAAAAT | 23072 |
rs532198801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43430772 | GTGGCCTCCATTTTT[A/C]TTTTTCTTTATTATT | 23072 |
rs532202982 | snp | C/G/T | 0.000106431 | 0.00729426 | missense, synonymous-codon | HECW1 | GRCh38.p7 | 7:43445485 | TGGGCCGTGGCAAGA[C/G/T]GAGCTGGCCGCCCCT | 23072 |
rs532205052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43542800 | AAACCAATTCCTTGG[A/G]AACTACTTCCTTTAA | 23072 |
rs532210542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43385458 | ACCTGGGAGCCTTAA[A/G]GAGGACAGATGCCCA | 23072 |
rs532223116 | snp | A/G | 5.05872e-05 | 0.00502902 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43541923 | ATTCCACCAGAGTTT[A/G]CAGTGGATGAAGGAC | 23072 |
rs532225789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206988 | ATTGCATTATCTTCC[A/G]AAGTCCTTTGCTGCT | 23072 |
rs532226114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214432 | AATAACTTTTCTGAG[A/T]AATAGGTACAAAAAA | 23072 |
rs532230388 | snp | A/G | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111154 | TGAGGTAAAAAAATT[A/G]TCCTTTATTGTGGTT | 23072 |
rs532235165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43379093 | ATCACCCTCACCTGG[C/T]AAAACCCCACCCTCG | 23072 |
rs532249159 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43208694 | TTGGTGGTTTAGGTC[-/T]TAGGACATGCTCCTC | 23072 |
rs532255927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43171312 | ACATACACACACACA[C/T]ACTCAGATGGTTAAG | 23072 |
rs532285515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43311052 | CTCATTTTAAGTGCT[C/G]AAAGTTGTAAACAAT | 23072 |
rs532297945 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43371628 | TTTATCAAAATTTAT[C/T]TTGGGCATATTTGCA | 23072 |
rs532297976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43386307 | CATACACCACAGAGG[C/T]AGGAAATCTTGGGGC | 23072 |
rs532298334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43338599 | AATTTTCCTCTAAGC[A/G]GTTTTTATTTTGCTT | 23072 |
rs532302115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160061 | AGCAAATTAAACTAT[C/T]GTTTCACTTCACATT | 23072 |
rs532316748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248397 | CCCTACACCATACCC[C/T]GCCCCACCACATCCT | 23072 |
rs532325976 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43343535 | GGTTTTCTGTCCTTG[A/C/T]AATAGTTTGCTGAGA | 23072 |
rs532329523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43439098 | GCAGTCACGTGTCAC[A/G]TGCAGTGTTTGCACT | 23072 |
rs532335219 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247724 | AGGGAGGGAAGAAGG[A/G]AGGAAGAAAGGAAGG | 23072 |
rs532347116 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112229 | TGTGCAAATACAGGA[C/G]GGTTCCTGAAATGTG | 23072 |
rs532352561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43295671 | GCGGCAGTGGAACAT[C/T]TGCATGACCTACGTA | 23072 |
rs532368090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43438227 | TGTAGGCTGCAATAG[C/T]ATAGTCTCACAGAGA | 23072 |
rs532369786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43446194 | GCTATTTTGGCTAAT[A/G]GAAGGGAAAAATAAC | 23072 |
rs532373157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117937 | GGTCTGAAGCTTGAT[G/T]CATATGGAGGCCTGA | 23072 |
rs532387044 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43239538 | TCCTTGAGGGGTTTG[G/T]GGTCACTGAAATAGG | 23072 |
rs532391130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43212911 | GCCATTTATATTATA[C/T]GGTAGATATTTTCCA | 23072 |
rs532394592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43436396 | GTGAAGAGACCACCA[A/G]ACAGGCTTTGTCTGA | 23072 |
rs532394919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122906 | TTTCAAATCATTTTC[C/T]GTTGCTTATTTATTC | 23072 |
rs532399516 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43220200 | TATTACAGTTTTATT[A/T]TAGCAAAAGGAGACA | 23072 |
rs532414536 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43386875 | TTTTGTTTACAAAAT[-/A]ATTAAAATAGCAGCT | 23072 |
rs532418351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43293099 | GTGGAAGGCGCCTGT[A/G]GTCCCATCTACTCTG | 23072 |
rs532419096 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43554425 | CTAAAACTTGACCTG[G/T]TTGCACAAATTGTTT | 23072 |
rs532422908 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | HECW1 | GRCh38.p7 | 7:43210469 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGGTATTGT | 23072 |
rs532437157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43252222 | TGCCTTCCCCTGCTA[C/T]GTGGGTCTTTCAGTA | 23072 |
rs532445747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43337631 | CACCTTTTCTTCTAA[C/T]AGTCTGACACTAACC | 23072 |
rs532452868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43377400 | CGCTTACTCAAGAGT[C/T]TGTGGTTCACTGTGA | 23072 |
rs532466891 | in-del | -/T | 0.439641 | 0.162899 | intron-variant | HECW1 | GRCh38.p7 | 7:43527383 | CTCCAGGGGAGACCC[-/T]TTTTTTTACCTCTTT | 23072 |
rs532482787 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546293 | TGGCTCTGTCATAAA[C/T]CCTGGGAGGTTATGC | 23072 |
rs532483637 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43353077 | TGTGTATAAATATAC[A/T]TATTTATAGTGGTAG | 23072 |
rs532508131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117387 | CCTATAACATCCCCC[A/G]CATACATAAGCCATA | 23072 |
rs532520557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43477737 | ATTTTTATCTCAATT[A/G]TGAAACCACTTCCTG | 23072 |
rs532520801 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43364441 | TCACTGAGAACTCAC[A/G]GTTACTCCATTATAA | 23072 |
rs532526072 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43288843 | TTGGTAATTCAGCTC[A/G]AAGACAAATTCTTCT | 23072 |
rs532529104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428936 | TACAGACATAGACAG[A/G]ATACATATATGTGTA | 23072 |
rs532535802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43252789 | TTATAAAACACCTAA[A/G]TGGTTACTGGGGGAA | 23072 |
rs532541865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43164052 | AGCCAGGGCAGGCAG[C/T]GAAGAGAGCGGTTGG | 23072 |
rs532546609 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43255147 | TGACAAGTGTGCCCA[A/G]TGTGATCCAAGGAGC | 23072 |
rs532549843 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43413016 | TAAATCTAGATCCCT[C/G]AGGAATCGCCACACT | 23072 |
rs532552386 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562537 | TCAGCCGGAACTAGC[C/G]TAGACATACGGTGCA | 23072 |
rs532553365 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43350071 | TGGTAATGGCAAATT[C/T]TCTCAGCATTTGTTT | 23072 |
rs532564593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43273044 | GCAGCGGGAGGCCAT[C/T]AATACTAAGCAAATT | 23072 |
rs532566782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43194384 | GCTCGTTCATTCTCT[G/T]ATCAGTTCAGATGCA | 23072 |
rs532586397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43391242 | GCTTAGAAGGTATGT[A/G]AGTTCTGGAAAACTT | 23072 |
rs532586814 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43417990 | AAGTCCAAAATGAAG[C/G]TGTGGGCAGAGTTGT | 23072 |
rs532588488 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43388184 | CCTGTGACCACCTCC[A/G]TAAATGCTCCCAACC | 23072 |
rs532588523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43259985 | AATTCTAAGTAGTAG[A/C]GACACAAATAAAACC | 23072 |
rs532598590 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43281096 | GGCGATTTCTGACCC[A/G]CTGCTTCTCATCACA | 23072 |
rs532611954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43384506 | GTGGCATGTCCATAG[A/G]AAAAAAGATGTTACA | 23072 |
rs532626585 | in-del | -/GAA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247842 | AAGGTAAGAAGGAAG[-/GAA]GAAGGAAGGAAGGAA | 23072 |
rs532631403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43364533 | AGAAAGCCGTGACCA[A/G]GCACCTGCAGCAGCT | 23072 |
rs532631789 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43110859 | GTATATGCTGCCATT[G/T]CACCTGACATGTAGA | 23072 |
rs532645641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43375171 | AGGAAGAATTTTTGA[A/G]CTGAAGAATGCTATA | 23072 |
rs532659466 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43324522 | CTACGAAACGTTCTC[A/G]TATGGCTATCCTTCC | 23072 |
rs532668958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43457731 | AGTGAGCTGACATCA[C/T]ACCACTGCACTCCAG | 23072 |
rs532672941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43406241 | CCCAAGACCATGCTT[A/C]TCTGTGAGTTCCCTA | 23072 |
rs532676586 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43383415 | TAGTGTAAAAATATT[C/T]CTGTTTCTCCACAGC | 23072 |
rs532687088 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43555662 | ATAGCTTTCACCTAG[G/T]TTTCCCAGATTTTCC | 23072 |
rs532688189 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43527224 | AGGTGTTCTGGACAA[C/G]CAAGGAGGAGGGCTA | 23072 |
rs532688290 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562820 | AACTGGAGAAAGGGA[A/G]GAAGGACATATTACC | 23072 |
rs532695533 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43172953 | TAGCCCTTGAATGTG[C/G]CTTTAAGCACCCACT | 23072 |
rs532700569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520070 | CCATTTGGTAAAAAT[A/G]TCTTAGCTTAATTAT | 23072 |
rs532706889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43423299 | TCTAAGTACAAAAAC[C/G]AGTTCTTTTGTTAGT | 23072 |
rs532706958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412295 | ATCACATTGTATATA[C/T]ATTATAAACCCTACA | 23072 |
rs532712379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43233457 | TCTGTAGAATCTTAA[A/G]ATATTATCCAGTGGA | 23072 |
rs532717307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43371024 | TCCCGAGTAGCTGGG[A/G]CTACAGGTGCCCGCC | 23072 |
rs532719233 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43280280 | TGCAGGAGTGCAGGG[C/T]CACAAGATGGAGTGG | 23072 |
rs532723282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513794 | ACTTATTTGTACGAC[C/T]GACTTCCAAACTGAA | 23072 |
rs532726400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420927 | GAGATATGTTAATGT[A/G]ACTTGACAAGCTAAT | 23072 |
rs532726945 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43188121 | GAATGTGGTTCCAGA[C/T]TGAGGATGTCTCTTC | 23072 |
rs532727959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43507791 | TAAAAGTAGTTCCAT[A/G]TGATGGAATGCACGA | 23072 |
rs532736242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152071 | TGCCTGATGACAAAG[A/G]AGCAAGATTCACCAA | 23072 |
rs532736667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43192245 | ATTACAGGCGTGAGC[C/T]ACCACGCCTGGCAAG | 23072 |
rs532753849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328766 | AAAACGATGGTGCCG[G/T]CTTCCAGTCAGATAC | 23072 |
rs532759207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43429618 | TCATTTTTAAACCTA[A/G]TGACTAGTGCCACCT | 23072 |
rs532762945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520470 | CTGCCCATATGTGCG[C/T]GATTGTTTCTTCTGT | 23072 |
rs532772840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43193946 | CATTTCAAAATATGT[C/G]AAAAAAGATATTTTG | 23072 |
rs532780528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518453 | GTGGGCCTGGATTGC[A/G]CCACTGCACTCCAGC | 23072 |
rs532805613 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43404283 | ATTTGCTGAAGGACA[A/G]GAAAGAAGACCTGTA | 23072 |
rs532809944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427408 | TTCTCTTCAGAGCTC[C/T]TTTTCTTAGAATTGT | 23072 |
rs532816919 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43317327 | ATGGCCTGGACAGCA[G/T]CCTCCTGCCCTCCAG | 23072 |
rs532829986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375853 | AGCCATGATCAAACC[A/G]TTGTACTCCAGCCTG | 23072 |
rs532837708 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43416626 | GGCACCCCTCCCCCA[A/G]CCTCGCTGCCGCCTT | 23072 |
rs532846885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43411386 | ATTTATCAAGCCATG[A/T]TTTACAGTCCAGCAT | 23072 |
rs532850266 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162497 | ACAAGGACACTTGTC[A/G]TTGGATTTAGGATCC | 23072 |
rs532852928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43553713 | TGGCTGTTAAGGCCC[C/T]ATAACACCCCCCGGA | 23072 |
rs532858364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43462604 | TGTTTTAAGTCCTGC[A/G]GGTGATTCTGCGTAG | 23072 |
rs532862577 | in-del | -/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126088 | TTTTTTTTTTTTTTT[-/TT]TGGTTTTTACTCACC | 23072 |
rs532868553 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43188749 | ATGAGACTCCTGCCC[C/G]CGTGCCATATCTGGC | 23072 |
rs532874006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43561128 | GGTCCAGGTGTTAGC[C/T]TCTGGCGAGGAAGAC | 23072 |
rs532886149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43321976 | AACGAGGAAATTTTT[A/G]TGCTATCAGGGTGTA | 23072 |
rs532897368 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43415174 | GCTGGTACCGGTTGT[C/T]CCTTTCCATGTTTAG | 23072 |
rs532909029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43410725 | GTCATTTAGATTACC[A/T]ATTTCTTCTAAGAGA | 23072 |
rs532921613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376335 | AAGGAAGGGCTTTTT[G/T]ATCATCTCTGACTGC | 23072 |
rs532926908 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512418 | TGTTGTTGGTTTTTT[C/T]CAAAAATAGAAATTT | 23072 |
rs532927319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43547940 | TACACAGTTTACTGG[A/C]GAGAGGCTATTCATC | 23072 |
rs532937581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43369185 | AATTTAGGGCCGGGC[A/G]CAGTGGCTCATGCTT | 23072 |
rs532945095 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43503531 | ATTTGGATATTCTAA[A/G]AGGAATAAACTTTCC | 23072 |
rs532961392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43548381 | TGTACGAGTGGACCC[A/C]TGCAGTCCAAACCCA | 23072 |
rs532966908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43176044 | CTCAGCAAAATGTTT[A/G]CCTATTTTGCAAGTA | 23072 |
rs532968947 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43534749 | TTAACTGTGCCAGGT[A/G]CCATGATACATAAAT | 23072 |
rs532980293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43198693 | CACACCACACACACC[A/G]TACATACACCCCCCA | 23072 |
rs532980397 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43205803 | TTCAGGTCCCTTACT[C/G]TCATTTCAGGGCAAG | 23072 |
rs532985441 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43284320 | GTCAAGCTAAGTAAC[A/G]TATGCATTATCTCAC | 23072 |
rs533003078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43187545 | ATTACCTTTTACTCA[C/T]TCTAAAATCGTTTTT | 23072 |
rs533015390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43450518 | TCTGCTAATTTTCTC[C/T]TGTGTTCCTTTCTGG | 23072 |
rs533016281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43455640 | TTTCTAAAGAAATAA[A/G]TTCATTAAACAGTAG | 23072 |
rs533025469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116406 | CTCTAAGTCCTGGTT[C/G]TATCAACCAGAGCTT | 23072 |
rs533025850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43181851 | GGAGTGCAGTGGTGC[A/G]ATCTCCACTCACTGC | 23072 |
rs533027415 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43362625 | CCTGACACCTGTTAG[C/T]CAATCATTGAGGGTG | 23072 |
rs533031224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43404269 | AGAAAAGTGTAAACA[G/T]TTGCTGAAGGACAGG | 23072 |
rs533031809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142887 | TCTGTAAAATCGACA[C/G]GTCCCAGATCTGTAA | 23072 |
rs533038015 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43308648 | TTTTTTTTTTGAGAC[A/G]GGGTCTCGCTCTTGT | 23072 |
rs533053281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43461979 | CTTCAATTTCTGTAA[C/T]TTTAACAATCACTCA | 23072 |
rs533062088 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43249487 | CTTTCAAAGTAAGTG[C/T]TTTTATCAAGGGCCT | 23072 |
rs533075100 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215398 | GGCTAGACGGCAATC[A/C]TACGTAATGCTATGG | 23072 |
rs533094128 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149746 | AAAAATATTTACAGA[C/T]ATATTCTTCAAAATT | 23072 |
rs533095584 | snp | C/T | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111427 | GGTCTGCTTTGAGCT[C/T]ATCTGACCAGAAGAT | 23072 |
rs533096859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43329094 | GAGGAGGAGCCCTAG[C/T]CTGACCTTGGGGCAA | 23072 |
rs533108691 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43211671 | TAACCCTTCACAAAA[-/G]GGGGGGCGTTCCCCC | 23072 |
rs533119473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43264453 | ATTGAATAGTATTCC[A/G]TTTTCTATGTATACC | 23072 |
rs533120669 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43265689 | TCAATTCTGGCACTC[A/G]CTCCTGGAGTTAGCC | 23072 |
rs533123605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43504366 | TCCACTACCCTTCCT[A/G]CTACCACCCTTTGGC | 23072 |
rs533125055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128419 | TGTGCTCTGTAAATG[A/G]AACAATGAAGCTTGA | 23072 |
rs533147841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43361626 | AGATGCCATCTTCCT[A/C]AGTTACAATCCAGTT | 23072 |
rs533149105 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43539961 | GCCCAAGGACCCATT[G/T]TCCCAGAAGCCCCCT | 23072 |
rs533157057 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43489044 | AGGCCAGGAATAGAA[C/G]TGAGCCTCTTTCTGT | 23072 |
rs533157834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43355921 | TTGAACACAGGAGGC[A/G]GAGGTTGCAGTGAGC | 23072 |
rs533159261 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43361048 | TTTCCTATTTTGTTC[G/T]TGTGCGTGCGTGTGT | 23072 |
rs533166858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43363169 | AAATTAAGCAAGAGG[A/C]CAACTGCCCAGAAAA | 23072 |
rs533169162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43454821 | ATCTGACCTACTCCC[A/G]AAAGCTATGGCTTTT | 23072 |
rs533170304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43225167 | CTCACCCAGCTATCA[C/G]ATGGTGGCTGGACTG | 23072 |
rs533173021 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43143377 | CAGCCTCAACTTCCT[C/G]GGTTCAAGCAATCTT | 23072 |
rs533178686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511249 | GTTCTCCCTCATGTG[A/G]AGAGTATTTGTGGTG | 23072 |
rs533193638 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43272156 | AGCAGAAGAATGAAA[A/C]TGAATCCCTATCTCT | 23072 |
rs533208731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43265153 | TCATTGTCCTAGTCT[A/G]TGGGTCGGGAGGGTA | 23072 |
rs533222585 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43306310 | TCTGTTTTGTATTTT[A/C]CTATTTTATTATACA | 23072 |
rs533252565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126897 | TCAATAACTGTGGTG[C/T]GTGTTCTGACTCTTC | 23072 |
rs533255515 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43286999 | GTGTCCCGGGCATTG[C/T]TTAATGATGGTTGGG | 23072 |
rs533255729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43493686 | AGGGATAGCGATCTG[A/C]AATGATAAAAAGAGA | 23072 |
rs533255944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43398380 | AAACAGTCTTTAAGG[C/G]GACACAGCGGCATAA | 23072 |
rs533262825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43395088 | CAAGTGCAGGGTCTA[C/T]GAAATATCTCAAACA | 23072 |
rs533264875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43390460 | GTGGGAGGACCACTT[C/G]AGTCTAGGAAGTCAA | 23072 |
rs533270511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43174411 | TTTCTGCAGCTATTC[C/T]ACTCCTTGATCCAAA | 23072 |
rs533277634 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43176685 | AATAGGTTAACCCAT[C/G]CATGAGGGCAGAGTC | 23072 |
rs533278239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43403546 | CTTTTGGGAAAATAG[C/T]GAGAGGGCAAAGAGC | 23072 |
rs533287693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43219126 | ATGCAAATACAGGGC[A/G]CCATGATGTTCTACA | 23072 |
rs533287872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43260251 | GGTTAAGGGATCAAG[A/G]CAGGCTTTCTGAAGA | 23072 |
rs533293511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43500242 | ATAGCTGGGATTACA[A/G]GCAGGCAACACCACA | 23072 |
rs533295380 | snp | A/G | 6.65469e-05 | 0.00576793 | missense | HECW1 | GRCh38.p7 | 7:43493147 | AAATGCTGCAAGAGC[A/G]TCAGCCAAGCTTAGC | 23072 |
rs533295669 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43252523 | TTTAAGTTGGGAACA[A/C]CCTGGCTTATACCAT | 23072 |
rs533322454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43204162 | CCTTCTTCAACAGTA[A/G]ATGTCAAAGCAGCTA | 23072 |
rs533324501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43491896 | GCTTTCTTAACCATA[A/G]TATAGCACATCATCA | 23072 |
rs533330040 | in-del | -/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130723 | GGATCAATTGTGTGT[-/G]GTGCACATGAATTTT | 23072 |
rs533335133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523917 | AGCCTCTGTCCTCCA[G/T]CCCTTCTTCCAGTAT | 23072 |
rs533337636 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43556706 | TTAAATTAAAAAAAA[A/G]AAAGAAAGAAAAAAG | 23072 |
rs533342039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43313430 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 23072 |
rs533342044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43321053 | ACTCCATGGCTCCTC[C/T]GGGGGCATCTCCAAT | 23072 |
rs533342829 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43461172 | GCCCAGCTAGGCAGT[A/T]CTCTCCCAGAATATC | 23072 |
rs533343044 | snp | A/G/T | 8.27136e-05 | 0.00643047 | intron-variant | HECW1 | GRCh38.p7 | 7:43442511 | ACCAGAACTGTGATG[A/G/T]TGCTTATTTCCTTCT | 23072 |
rs533343377 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43168841 | CTATGCATGTTAAAA[C/G]ACTGACAAGATATGA | 23072 |
rs533349046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405318 | CCCCTAGGTTCAACA[A/G]TTTGCTAGGAGGACT | 23072 |
rs533352431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43531619 | CTGGCTTTCTCCACT[A/G]CCTCTCCTCCCATTC | 23072 |
rs533384039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257644 | TGGTTAATGTTAACA[C/T]TATTAATTATTACTA | 23072 |
rs533400949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43524767 | CCCAGGTTTGGGGCT[A/G]TTGTTTCACCTCTAG | 23072 |
rs533402982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43544981 | AAAAAGAGTTTATGT[C/T]GATCAGGCACAGTGG | 23072 |
rs533416772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298290 | TATTAAATTTTCACG[C/G]GAATAAGTCCTAAAT | 23072 |
rs533418048 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43381912 | CAAGCAGTCCTCCTG[A/C]CTTGGCCTCCCAGAG | 23072 |
rs533420469 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43233205 | GAAACAACAGTTACT[-/A]AAAAAAAATCACAAT | 23072 |
rs533434276 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43424322 | GGAAAAAAAGTTACT[-/A]AAAAAAATACGAACA | 23072 |
rs533438833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43284107 | ACTCTAAAGCAGGAC[C/T]GTGGGGCGGGGACCC | 23072 |
rs533449988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43217461 | TATAGTTGAATGTCT[A/T]TATCAAATTAATGAG | 23072 |
rs533450000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43210081 | ACAGCCGGGGACTGG[A/C]AGTTTCCTGGCCTGA | 23072 |
rs533451924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135102 | TTGTTATAGGCTGTT[A/G]TCTATCTACCAATAT | 23072 |
rs533452606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43198246 | CGCACATCCCACAGT[C/G]TCTCACACACCCACT | 23072 |
rs533463831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43491223 | CAAGTATTAGAATCC[C/T]GGTTATCCCCCTGTC | 23072 |
rs533465691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43389632 | TGCTGTTGTTGTTGT[C/T]GTTGTTGTTGTTGTC | 23072 |
rs533486582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43181126 | GTGCCTGGCTTATTT[C/T]ACTTAACATAATGTC | 23072 |
rs533487602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43434690 | TGGCATGGAGAAAAG[A/G]GCCTGGTGGGGAGAG | 23072 |
rs533490354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43256878 | AGGTATATAAACCAT[G/T]TATTGACAATCACTT | 23072 |
rs533496494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43223525 | TCGGGAGGCCGAGGC[A/G]GGAGAATCGCTTGAA | 23072 |
rs533499149 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43540500 | GGAAGTCAATGCTCC[A/G]ACAAGCATTTAAATC | 23072 |
rs533499424 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43467016 | AGTTAAATTTCATAT[A/G]ATTTTACATATGTAG | 23072 |
rs533504140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43314190 | TCCTCAAGTTAGGTA[C/T]CCACTGGAAGAGAAG | 23072 |
rs533505037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43305773 | CCAGCTAATTTTTTT[G/T]TTTTGAGACGGAGTT | 23072 |
rs533527803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43482809 | TCTCGGGAGGCTGAA[A/G]TGGGAGGATGGCTTG | 23072 |
rs533539741 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43209524 | ATTTACAAGAGAGCT[-/TC]TCTCTCTCTCTCCTG | 23072 |
rs533558106 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43466975 | TAGGTTTCCTTTTGA[C/T]ATGGTTTTTTCGAAT | 23072 |
rs533559585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43403910 | TAAGTATTATAATAA[A/G]TGTACATATGTCTAT | 23072 |
rs533566043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43433818 | AGAAGATGAGGAGCC[A/G]TTTATTCATTGGTTG | 23072 |
rs533581117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43432113 | GATTACAGGCATGAG[A/C]CACTGCACCCGGCCA | 23072 |
rs533587638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210579 | ACCTGGGGTTCTTGG[A/C]CTCATGGATTCCAAG | 23072 |
rs533587809 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43216289 | TAGCTGGGACTACAG[G/T]TGTGCACCACCATGC | 23072 |
rs533592431 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43468563 | GCCTTGCTCTGTTGT[C/G]CAGGCTGGAGTGCAA | 23072 |
rs533593037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43264752 | CGGTGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 23072 |
rs533597335 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43530875 | CCTAAAATCTATATC[C/G]TTCATATGGGTGCAA | 23072 |
rs533600372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299675 | TCAGCAGTAAGTGTC[A/G]CCTGAGACGTTTAAG | 23072 |
rs533603137 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43442727 | TTCTCTCCAGATGTA[C/T]CCTAGGTTTTGTGGT | 23072 |
rs533609844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43250338 | TGGATGTTGTAGATG[G/T]GAGCATGGACCAGTC | 23072 |
rs533610784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43531943 | CTGGCTTCAAATGCC[A/G]TCTGCATCCTGACGG | 23072 |
rs533624568 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43198136 | CACTATAGTCACACA[A/C]CCCACACTCTCTCAC | 23072 |
rs533631434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389978 | AGATCTTTGCCTGAA[A/G]GAGATGTATTCCTGG | 23072 |
rs533631804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121789 | TGCTTATTCTTCACT[C/T]TCCTGTCTTTCAGCC | 23072 |
rs533646501 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43538844 | AACCGCGGTGACTAG[A/G]ACTGACAGAATATTG | 23072 |
rs533651706 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43328234 | TGGGAAGCTGAGATG[A/G]GAGAATCACTTGAGC | 23072 |
rs533661289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43169335 | TGGGGGCTGACCTGC[G/T]CATGGCAGGGTGTGA | 23072 |
rs533676661 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43204767 | TAGGCCATCTGAGTT[G/T]GTTAATTGACACTTA | 23072 |
rs533684376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43307443 | GGAGGGCCACCCTTT[A/G]CAGAGAGGAAAGAGA | 23072 |
rs533687403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43474977 | CCCAGGGGCTTCAAG[A/G]AGTAGAAAATGAGGA | 23072 |
rs533723874 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43258089 | TCACGCCTGTAATCT[C/G]AGCACTGTGGGAGGC | 23072 |
rs533737802 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43265214 | GGTGACAGCCACCAT[A/C]TCTGAGGTTGCCAGT | 23072 |
rs533749201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43435273 | AGAATGGAATAACTG[C/G]ACCAAAGATATAGAA | 23072 |
rs533749831 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43507384 | GTTATGGTCTGAAGC[A/G]GGGGAAGAAGGAAGT | 23072 |
rs533752190 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43136473 | GCTGAAATTACAGGG[A/G]GGTTCTCTCATCTCC | 23072 |
rs533755675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43224763 | GAGGCTGCAGTGAGC[C/T]GTGATTGCACCACTG | 23072 |
rs533756821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43117501 | TTTCTACTTTCTGAG[G/T]TTTATTCATTACCAT | 23072 |
rs533757383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300312 | CTGGTGTGGCTAAGG[C/T]GTGTGGCAGCCAGAA | 23072 |
rs533771137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43292586 | GCCCAGAGCCTGAGA[C/G]GGAGCTCAGGGGACA | 23072 |
rs533774154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135663 | TCATGCATAGCTTTT[G/T]CCTTTGACCCATTCT | 23072 |
rs533812959 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43544322 | TCAGTCAACAACCTA[A/G]TAGAAAAGTCACAAA | 23072 |
rs533812973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43199753 | ATCCAAAATGTATCT[C/G]TTACTGAGTAGGAAG | 23072 |
rs533820922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43470074 | CTCCAGGACCAGCTC[C/T]TCTGTAACCAGGGAT | 23072 |
rs533835791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43450113 | TTGAGCTTTCCTGTC[A/G]CCGTCTTTCTGCTTT | 23072 |
rs533839750 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43487465 | CAATTATGGAAGAGT[G/T]GTTGCAGCATGTCTG | 23072 |
rs533846604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43561452 | GGGCAAGAAGACTTA[A/G]GAATATAATCCTTCA | 23072 |
rs533857445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43477165 | TTCTAAGAGTTCTTT[C/T]AAAATTAGTATTTGT | 23072 |
rs533860316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43256470 | CAAAATTAGCCAGCC[A/G]TGGTGGCAGGCGCCT | 23072 |
rs533860363 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43284587 | TTGTCAATTTTCAAG[A/T]TCAATACCTTGTTAT | 23072 |
rs533861864 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43393184 | GCTTCAACAGAGAGA[-/G]GGGGGGGCAACAGGA | 23072 |
rs533862775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43484196 | GTGTGTTCCAGCTGT[C/G]TGATTCTCAGAGTCT | 23072 |
rs533870861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43428502 | AGTTAGGAAGTAATT[A/G]CAAGGACAAGGAATG | 23072 |
rs533876719 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43210889 | AAGCTCAGGTCCAGC[C/T]GTGACAAACACGGAC | 23072 |
rs533878964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43285659 | TATTAAAAAATTTTT[A/T]AAAATAGCTGGGTGT | 23072 |
rs533883249 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43231694 | CGGTGGCAGCATTGA[A/G]GAGGGCACACAAAAT | 23072 |
rs533889659 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160976 | CTCTCCATTTCTACA[-/C]GGTTTTTTTTTTCTC | 23072 |
rs533891710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43250585 | GGTGGAGAAGAGAGC[A/G]CCAGGAACGTCCTGT | 23072 |
rs533897844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43388411 | GATCTAAAATGCCAT[G/T]GACTTTCAGACCAAC | 23072 |
rs533901492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43492485 | CCCGTGCACAAGAGC[A/G]AGGTTTAAATGAGGT | 23072 |
rs533920186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161860 | GTCACTTGTGTGTAT[C/T]TGTGTCCTCTGTGCT | 23072 |
rs533921037 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43403798 | GTTTGGCAAAGGTTG[C/T]CACTGGTGGGGAGGG | 23072 |
rs533923464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43499898 | AAAGGATCAGAATAC[A/G]CGAGTTGTAGCTGAC | 23072 |
rs533925653 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43445661 | AGAAGGGCGGGGGAT[-/C]GGTGTCAAACGGGGT | 23072 |
rs533946981 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43258834 | TTGAGTTGGGCAACA[A/G]TTACATTGCTGATGG | 23072 |
rs533949634 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43229368 | TAGCAAACTAACACA[C/G]GAACAGAAAAAAACC | 23072 |
rs533961403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516867 | TTACTGTACTGAATA[C/T]CTTAGGCAACTGTAA | 23072 |
rs533965796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43293408 | GTGGTAGCCCACAAT[C/T]AGTCTGATTGGTTAC | 23072 |
rs533966786 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43542826 | TTTAATAAATCTGCC[C/T]GTGTCCTCTTTCTTC | 23072 |
rs533985458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43343225 | CCATGATGTTCAGAT[A/G]TTCACGGTGCTGGCA | 23072 |
rs533989386 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43188935 | GACTGGTTCTTTTAA[A/C]CAGCCTACATTTAAG | 23072 |
rs533989717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517337 | AATAAACAGACTCCC[A/C]TGCCCCCTTCTGCCC | 23072 |
rs534000830 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43238251 | AGGGATGGCACTGGT[G/T]GGGAGGGGTCCCAGC | 23072 |
rs534005396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43251938 | TGTCATTCATCCAAG[C/T]TGGACCCAGTGCTCT | 23072 |
rs534016293 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481767 | AGGCAGGCAGATCAC[A/G]AGGTCAGGAGATCAA | 23072 |
rs534017662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43381338 | ATTTATTTACTTCTT[A/G]GAGGCAAGAGTCTTG | 23072 |
rs534023596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43283560 | TTAATTTCTAACATA[A/G]TAAATACTGATAGAT | 23072 |
rs534031165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380738 | TTCACCATGTTGGCC[A/G]GGTTGATCTCAAACT | 23072 |
rs534039990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157876 | AATACATTATTTTCA[A/G]AATCATATTTCCTCA | 23072 |
rs534041020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162452 | ATGGTCTGCCTCCTC[C/T]TCTCTCTGTCTCTCC | 23072 |
rs534041600 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43169721 | TTTGAGACGGAGTCT[C/T]GCTGTCGCCCAGGCT | 23072 |
rs534043147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43482916 | TCTCAACAAAACAAA[A/G]CAAATAATAAAATAA | 23072 |
rs534045363 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43263481 | TTCTCATGCCTCAGC[A/C]TCCCGAGTAGCTGGG | 23072 |
rs534058513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43239520 | AGAGGCGGGCCGTAA[A/G]TTTCCTTGAGGGGTT | 23072 |
rs534064577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43449010 | CATTGCATTTGCTTG[A/G]GGTTCACAAGCAGGT | 23072 |
rs534065752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43290654 | ATGTCTGAATTTTAT[C/T]TTTGGTTTACAGTCC | 23072 |
rs534083910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43245767 | AAACAAAACATGAGC[A/G]TCAGTACAGCCTCCT | 23072 |
rs534093461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43286146 | AGCTCAGGACCCTGA[A/G]AGGGTGGATGACTTG | 23072 |
rs534099048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43277628 | GACCATTTCCGTAGG[A/C]ATCCACCAGCAATTT | 23072 |
rs534111127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511432 | CTGAATGCCTCAGTC[C/T]CGAGAGTCCTCAGCC | 23072 |
rs534121532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43420403 | ATATATTTCCTTAGA[A/G]CCAAGAACAAGACAA | 23072 |
rs534121688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148588 | AGGTAAACAGTGTTG[A/G]ATACTTAAATTTGGG | 23072 |
rs534126702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43336457 | ACAGGTGTGAGCCAC[A/C]ACTCCCAGCCAAGAT | 23072 |
rs534130660 | in-del | -/AAC | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513982 | GCAAAGCAGGGAAAT[-/AAC]ACTCTCAATCAACAC | 23072 |
rs534130686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43427047 | GAAAAAAAGGCCCTG[A/G]AAGTTTATGGTTGCT | 23072 |
rs534132655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43293152 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTAAGC | 23072 |
rs534133694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43277127 | ATAATATATGTGAAA[A/G]AGAAATCAGTTCATT | 23072 |
rs534143518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116779 | GTATGAAATGCTCTG[C/T]GGGGTTTTCTTCAGG | 23072 |
rs534158934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43375216 | ACTGTCGGACGCCTG[A/G]AAAATAGCAAAAGCC | 23072 |
rs534164256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43190852 | TGATTTAGACCCAGT[C/T]TTGTTTCTGGCTGCT | 23072 |
rs534176342 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145833 | TGTCACCTCCAGGGT[-/A]AAAAAAAAATAATAA | 23072 |
rs534182697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43441850 | AAGCTCACAACCACA[C/G]AAAAACAGGTGGTGG | 23072 |
rs534183406 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160962 | TAAATTTTATAACAT[A/C]TCTCCATTTCTACAG | 23072 |
rs534194414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523564 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 23072 |
rs534208768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43186200 | ATTTCTAACCCCTAC[A/G]TGATTTATTTGCTAA | 23072 |
rs534210488 | snp | A/C | 9.98868e-05 | 0.00706636 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43492116 | AGCCTCTTTACTGGC[A/C]AGGCCAGGACACAGC | 23072 |
rs534213108 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126961 | GCCTCGGGCCACCCT[A/G]TTCCCTGAGACACAA | 23072 |
rs534231969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43530651 | TTTCAGCTCTGACCT[C/T]TCTATTGAGCTTCAA | 23072 |
rs534243913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43553779 | CTCTAGTGGCTTACT[G/T]TTGCCTGCATATTTC | 23072 |
rs534247655 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43307023 | TCATTTAAGTTGGAA[A/G]GCAAAACAAATAAAC | 23072 |
rs534247824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43368766 | ACACCTTTCCCACCA[C/G]CTATGGTTCAGCTGC | 23072 |
rs534248864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43410246 | CGAAGCTGGGAAGTC[C/T]GAGCCCAGGATGCTG | 23072 |
rs534249462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43433945 | AGGATTGGCTTTGTC[A/C]TTTCCACACTGGTTT | 23072 |
rs534261345 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43405523 | TGAACTGTGACAGCA[C/T]GTGGAAATGCTGTCT | 23072 |
rs534270804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512062 | TAGCTGCTGCTGATC[C/T]CGGGTCGGTGTCAGG | 23072 |
rs534279998 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43556730 | AAAAAAGAAAAGACC[A/G]TGCTGAGGAGTCTCT | 23072 |
rs534298927 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43282951 | GGGAAAACCCCATCC[A/C]TACTAAAAATACATA | 23072 |
rs534303941 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389096 | TGTGGCCAAGGGGTC[A/G/T]CCAGAATCTAATTCT | 23072 |
rs534311172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509433 | CTAAAATCATAGGGT[C/T]CCAGTGGAAGCTTCT | 23072 |
rs534311393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154127 | GTATTGATTTCCTCT[A/C]TGGCAAAATACTTAT | 23072 |
rs534321808 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43432429 | CAGGTGTGAGCCACC[A/G]CGCCCGGCCCAGTTG | 23072 |
rs534325660 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43193628 | CTCAAGTGATCCACC[C/T]GACTCAGCCTCCCAA | 23072 |
rs534334941 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HECW1 | GRCh38.p7 | 7:43196034 | CCAGCTTGGTCCACA[A/C]CCTGGTTTTTCAGGA | 23072 |
rs534335531 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, missense | HECW1, LOC105375254 | GRCh38.p7 | 7:43113996 | TGGTTCCGGGCACAG[A/C]GCGCCTCAGTCTGCA | 23072 |
rs534338005 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43195884 | GGTGCCACCCATTTT[A/T]ACACCAAATATAGGT | 23072 |
rs534341735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43522581 | GCTCTCACCTGCCCC[A/G]CAACAGCCACCTCAC | 23072 |
rs534343035 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43164267 | TCAGCCATTGGCACT[C/T]AATAGTTATTATTTT | 23072 |
rs534345475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43328383 | GAAACATATCCACCT[G/T]CAGCAATCCCAGTCA | 23072 |
rs534379799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43460397 | TAAGCTTTTCTTTAA[C/T]AAGGAGTAGTTTCTC | 23072 |
rs534382041 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43226042 | CCTCCCAAAGTACTG[A/G]GATTATAGGTGTCAC | 23072 |
rs534392276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43230130 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23072 |
rs534392820 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43320051 | ACCACAGCCCCTGCA[C/T]CTTCCCCAGCATCTG | 23072 |
rs534412012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43334607 | TAGACTTACATTGCT[A/G]TTGCCAGCTGTGTTA | 23072 |
rs534414809 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43459724 | TGCATTTTTAGTAGA[G/T]AGAAGGTCTCACCAT | 23072 |
rs534415198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43467136 | TGGTTCAGGCTCAGA[A/T]CTAGGTGCTGGAGTC | 23072 |
rs534418965 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43286683 | GCCACCCACCCCCCC[-/A]AAAGGTGTTTGGGAG | 23072 |
rs534422751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43236389 | GTCAGTCAATTTAGA[A/T]AGTTTCTTTTGGCAA | 23072 |
rs534442841 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43328958 | AGGCCTGCTGGGGAT[C/T]GTGCTGGTCTCCAGG | 23072 |
rs534444648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43373187 | ATGCACGTTGGTGTC[A/G]TTCTGCCTTCTTCCT | 23072 |
rs534446530 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147103 | AAGACTATTAAAGTT[G/T]TCTGTTATCCAAGGA | 23072 |
rs534455998 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43362284 | CTAATTGAGGCCTTG[A/G]TAGTAAGCAGTAAGG | 23072 |
rs534460565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43326898 | AGCCAGAACAAGCTC[G/T]CTGGGACCAGAGGCA | 23072 |
rs534462359 | in-del | -/TT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156057 | AATAGTTAAGAACAC[-/TT]AACTGGGGGAAATAA | 23072 |
rs534464503 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43462382 | TCTGGCCCTGCCTGG[-/T]TTTTTTTTTAGCAGC | 23072 |
rs534472810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142509 | CCAGTCCTGGCTCTG[G/T]CTCAGCTCCCTCCCC | 23072 |
rs534473917 | snp | C/T | 3.33133e-05 | 0.00408112 | intron-variant | HECW1 | GRCh38.p7 | 7:43552197 | GTGTTTGGACCTGGA[C/T]GCTGAAGCCTAACCT | 23072 |
rs534476936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43322052 | GAGATAGGCATAATA[A/G]AACTCCCAGCAAGAG | 23072 |
rs534479874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43560515 | CCAGGAGGAGGAATG[G/T]GTGCTGGGCAGATGA | 23072 |
rs534482553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43497058 | ATATGTTAAGTGCCA[C/T]GAAGAACATGATTAG | 23072 |
rs534494335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43353667 | GGCACCAAGTGCATG[A/G]AAAATTTTTCCCCAA | 23072 |
rs534508806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43230951 | GCATTAGCACATCAT[C/T]AGGGCCCTCCAGCTC | 23072 |
rs534512407 | snp | A/C | 1.72752e-05 | 0.00293893 | intron-variant | HECW1 | GRCh38.p7 | 7:43469150 | TCAAACAGGCTCCTT[A/C]CCCAGGGTGAAGCTA | 23072 |
rs534528764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43546699 | AACAAAGCACTGACA[A/G]AACCAATCCAGAAAA | 23072 |
rs534533019 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43421031 | CAGGACTTTTATACT[G/T]CCGGATGTCCAGATA | 23072 |
rs534554817 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43272477 | TAAAAACTTAATTGA[A/G]CAAGCAAAAAACAAC | 23072 |
rs534559364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269765 | TGCATGCAAGAATAC[A/G]AAGCTGGGGGCGGGA | 23072 |
rs534560495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43504576 | CTGTCTGCTTCCCCC[A/G]CTTCTGCAATCAGGC | 23072 |
rs534574678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529771 | CCAGCAGTCATCCCT[G/T]TCTCATGGATCTTTA | 23072 |
rs534587285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516527 | GAAATCACCACTGGA[A/G]ATTCTTTTTGTCCCA | 23072 |
rs534587435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43417763 | AATAATAAATCTATA[A/G]TGATTTAAATCATTG | 23072 |
rs534588074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43447857 | ACGGCTGGGTGTGTG[A/G]GCTCACGCCTGTAAT | 23072 |
rs534588540 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43321898 | AGAAACTTATGGTAT[C/G]CCCGCTCCCGGCAAT | 23072 |
rs534591566 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43275294 | AAAATCTCTCATAAC[-/AT]AATGTTACATAAGTA | 23072 |
rs534601448 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43350564 | GTTCATGTTTTCTTA[C/T]TCTTTTTCCTTTGTC | 23072 |
rs534608013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43326502 | TGTCCTCCACAAGGC[G/T]GCCCCATGAAGATGA | 23072 |
rs534608613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43281894 | TCTTATGGCATCCTG[C/T]ATGTGCAAGAACTCA | 23072 |
rs534621259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43256550 | GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGATTGC | 23072 |
rs534628205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43380001 | AACATTTGTATCCAA[C/T]AAACATGGGTTATTC | 23072 |
rs534638474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43216232 | CTCACTGCAACCTTC[A/G]CCTTCTGGGTTCAAG | 23072 |
rs534642949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133621 | TATATTTCTCTCTTT[C/G]TTTCTCTGTTCCTTC | 23072 |
rs534644573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43497718 | TGTGGATGCAAAAAC[A/G]ACAGGAGCTGATGAC | 23072 |
rs534648155 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43434584 | CAAGTAGCTGGTCCA[C/G]AAACAGACAGACTTT | 23072 |
rs534649307 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510464 | CAATTATAAATTAAG[C/T]ACATAGTATGTTCTG | 23072 |
rs534649690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43372403 | TAGGGTACATGTGCA[C/T]AACGTGCAGGTTTGT | 23072 |
rs534661857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43399809 | AGTGACTAGGAATAT[A/G]AAGTTAGTAGCTAGC | 23072 |
rs534683932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43310761 | AATTTGCATTTGATT[A/G]GGTGCATAAGAAGTT | 23072 |
rs534686881 | snp | C/G | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150453 | GTGCAATGTCAGCTC[C/G]GTGCAACCTCTGCTT | 23072 |
rs534688342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222247 | AGCCTGGATCCATTC[A/G]GAGAACCTGGGTTTT | 23072 |
rs534694271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43318268 | TACCTGGGTGTGAAA[C/G]TTGTTATATCTCTGC | 23072 |
rs534695169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269074 | GTGCCATTCTTAATT[C/T]ATCCTCTCCCTCACC | 23072 |
rs534697720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43558507 | TTGCCCCTCTTCCCC[C/T]GCAAGAGGCAGTTGA | 23072 |
rs534698103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43184789 | GTTCTGCAGGCTGTT[C/G]AGGAAACACGATGCT | 23072 |
rs534706259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43190443 | GTCACAGTAGGGAAG[A/G]GGAGGGATAATGTAT | 23072 |
rs534715561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43416887 | CGCCCTGCTTCGGCT[A/C]GAGCACGGTGTGCGC | 23072 |
rs534724697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43319255 | AGCCGGGCGCGGTGG[C/T]GGGCGCCTGTAGTCC | 23072 |
rs534734822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43551609 | TGTGACTTAAGAAAG[G/T]CGAGTCAGATTTGTT | 23072 |
rs534735213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43418482 | ATGATCCATATGCTA[G/T]ATCTTCAGAGTCCCA | 23072 |
rs534743601 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511318 | ACTAGCAATCTAAAC[G/T]GAGCCCACGGTGATG | 23072 |
rs534751176 | in-del | -/GTGC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43480620 | TGAGTTTGTGTGTGT[-/GTGC]GTGCGTGTGTGTGTG | 23072 |
rs534755068 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43303427 | GTGGATTTTTTTTTA[G/T]GAGCGATAAGGCATT | 23072 |
rs534756482 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43451680 | TAGCTTTAACTTCAT[A/C]ATACTCCATTTAATA | 23072 |
rs534778189 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43534664 | TGGGTTTGTATAGTT[A/G]CGCTCCACTGGGATA | 23072 |
rs534778735 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120595 | AATCCAACCTCAGAA[C/T]TTTCTCTATGTCCAC | 23072 |
rs534779107 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43331001 | TATTTTATTTTTTTA[C/T]ATACTTTAAGTCCTA | 23072 |
rs534785437 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43401352 | AAAGTCCAAAAAGGA[C/T]GAGGGAAAAAAAGAT | 23072 |
rs534787377 | in-del | -/TTGTGTTG | 0.0611083 | 0.163768 | intron-variant | HECW1 | GRCh38.p7 | 7:43446149 | TTATTACTGTTGGTT[-/TTGTGTTG]TTGTTTTGTTGTTGT | 23072 |
rs534794510 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43431007 | GGCTGGTCTCCAACT[A/T]CTGAGCATTCCTCCT | 23072 |
rs534794863 | snp | C/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157720 | CACATGCCACCAAAC[C/G]TGGCTAATTTTTCTA | 23072 |
rs534800240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43542546 | ATAAACAAATATATA[C/T]ACATATATGCCATAT | 23072 |
rs534804798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43447345 | AAACAAAAAAGTCAC[A/C]TCCTTGCCCTTTAGA | 23072 |
rs534825984 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43460097 | CACTGTTTTTTGTCA[C/T]AAGGGCCTGCTAAAT | 23072 |
rs534827491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43503447 | TGTTAACATCATTAT[A/G]TGGGAGAGATATCAT | 23072 |
rs534838831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43311349 | CTCAGAGGTTAATAA[A/T]GATAATCATCGTTTG | 23072 |
rs534839000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43180134 | ATGCACTTTGCAGAG[C/T]CTAAAAGAACAAAAG | 23072 |
rs534840959 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43185160 | AGGGATGGTGGGGGG[G/T]AAGGGGCTGGCTTCC | 23072 |
rs534851086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43221681 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 23072 |
rs534855731 | snp | A/C | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159827 | TGGGACTACAGGTGC[A/C]CACCACCACGCCCGG | 23072 |
rs534858002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43544594 | GCCTTTGACTCAGCA[C/G]ACGTCTAGAAATTTG | 23072 |
rs534880479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297685 | GCATTGGGTTTGGCT[C/T]TAAGGATTCTTCTCC | 23072 |
rs534882044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43339051 | CTTTTTGTCATTCCT[C/T]TGAAGGTAACTATCT | 23072 |
rs534882981 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426505 | TTTAGTATTTTTCAT[A/G]CAAATACTGTTTTTG | 23072 |
rs534884926 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43216856 | GACGGGGTTTCACCA[G/T]GTTGCCCAGGCTGGC | 23072 |
rs534885645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43537110 | GGGGTGGCCTGCAAC[A/G]TCGGTCGAGACTCCT | 23072 |
rs534892330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207635 | TATCCTTCCCTCCCC[A/G]TTCCCTTGTCAGCTT | 23072 |
rs534898641 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112707 | CGAACCGGCCCCCTC[C/G]TCGCGCACACACTCG | 23072 |
rs534898973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43346085 | ACTGTTTTCCATAGT[A/G]GCTGTACTAGTTTAC | 23072 |
rs534899676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43264568 | TTACTATTGTCAGCC[A/G]GGCGCGGTGGCTCAC | 23072 |
rs534918399 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43112977 | TGTCTGCCGCCCCTT[-/C]CCCCCCCGCCCTTCT | 23072 |
rs534918927 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121125 | GTCCTGAACTTCCGT[A/G]TTTTTCTCCTGGCTG | 23072 |
rs534954630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43403000 | GGTTAAATAAATTAC[C/T]GTAGAGCCAAATTAT | 23072 |
rs534955290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43172307 | TCTAGATAAATAAAT[A/G]AAATAAAATACAAAC | 23072 |
rs534957279 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43386257 | TTGTTAAAGTCAGCT[A/G]TCCTGATTCCAGAGT | 23072 |
rs534960210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43394613 | GGAAGATGAATAAGG[A/G]GTATGGCATCCAATG | 23072 |
rs534960968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43305309 | TGGAGGAAGAAAAAA[G/T]TCCCTGTATTCTGAT | 23072 |
rs534963753 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155055 | ACTTAGGGAGCCTGC[C/T]TTTTGCTTTCAAGTC | 23072 |
rs534984468 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43555118 | CAAGGACATTAATAT[A/G]AAAATGCTGGAACCT | 23072 |
rs534988877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43501772 | GCAGGTTGAGGCTGC[A/G]GTGAGCTATGATTTC | 23072 |
rs534989671 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43231862 | TCTACTAAAAAATAC[-/A]AAAAAAAAAATTAGC | 23072 |
rs534994543 | snp | G/T | 0 | 0 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563982 | ATACATTATAGAAAT[G/T]TAGACTTTTATTGTC | 23072 |
rs535000164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43227288 | GAGAACAAATGGTCA[C/T]TTTTTTTTAGGGGTG | 23072 |
rs535001730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43220801 | CCTTCCACCCCCATG[G/T]CCTGCCCTGGAACAA | 23072 |
rs535003237 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43289141 | CAGAGTATCGATCAC[C/T]CTGTCACCAGGCTGG | 23072 |
rs535025205 | in-del | -/TACT | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157449 | ACTGTAATATTCAGA[-/TACT]TACATGAAAACCATT | 23072 |
rs535027602 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248806 | CCTCCTCATAGTTTT[A/C]AGGGTCGGAGTCCTA | 23072 |
rs535039181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296706 | AATGGAAAAAAGTAA[A/G]GCTGATGAGTTCATT | 23072 |
rs535061154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43185255 | ACTCCCCATGCCCCA[C/G]AGCTTGCTCTGTGTG | 23072 |
rs535065870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43458910 | TGTGAAAATCAAATG[C/T]GTTTGTGCAAGGAGA | 23072 |
rs535083655 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43229009 | TTTATAGCTTTCAGA[C/T]TTTCCACAGTACGAA | 23072 |
rs535085691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351591 | GACATCTACTTGTTA[C/T]GGAACATATGCCTGT | 23072 |
rs535093963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43393187 | TTCAACAGAGAGAGG[C/G]GGGGCAACAGGACCC | 23072 |
rs535095939 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43266118 | TTGTTGGATCAGTCT[C/G]TACCCCTTCCCATTC | 23072 |
rs535097649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131708 | AACTTGTCAGTGCTC[A/G]GCGCTATGATTTAAA | 23072 |
rs535102687 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156322 | GGTGTTCACTGAATT[A/G]AGTGAATGAATTATG | 23072 |
rs535103052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43426289 | GAATACGGCAAGATA[A/G]AATATATTTAAATAT | 23072 |
rs535103754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43262172 | GTTGCAGTGAGCTGA[A/G]ATTGCGCCACTACAC | 23072 |
rs535115782 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43308060 | TATATATAATACAAC[-/AT]ATAATATATAAATAT | 23072 |
rs535127959 | snp | A/G | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511479 | CCCCTTCACCTCCAC[A/G]GGGTCAGAGATCAGA | 23072 |
rs535128298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43559287 | AATGGCATGGAATTC[A/G]ACACAACTTAAAGAC | 23072 |
rs535130362 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | HECW1 | GRCh38.p7 | 7:43223343 | TTTGTCAAGGCCAGG[A/C/T]GCCATGGCTCACGCC | 23072 |
rs535130978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43171529 | GAAAGGACAATGCTC[A/G]GGAGCTCCATGTTCG | 23072 |
rs535156468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43495708 | TAAGAATTCTCTCCC[C/G]TGGTTTCATTACTGC | 23072 |
rs535158049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131139 | GGCGTGGTGGCACAC[A/G]CGTGTAATCCCAGCT | 23072 |
rs535167787 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HECW1 | GRCh38.p7 | 7:43313636 | GCCACTGCCCTCGGC[C/T]GCATATTTTGTTTCA | 23072 |
rs535178011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248069 | AGGAAGGAAGGGAGG[A/G]AGGGAGGGAAAACAA | 23072 |
rs535182888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43488649 | TCCTAGCACATACTA[A/G]ATCCTAGTTCAAACA | 23072 |
rs535184899 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43245680 | CTGACATTTATGTGA[C/G]TGAGTTCTCACTGGG | 23072 |
rs535192382 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43429861 | CCCCCTTTATATCTC[A/G]CTGCAAGAGAGGAGA | 23072 |
rs535196550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43552965 | CTTGCAGAGAACATT[C/T]CATCCAGGACCCAGC | 23072 |
rs535203451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43460834 | CTGCCTCTGTGCTTC[A/G]GCAGAGGTCAGACGT | 23072 |
rs535207094 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | HECW1 | GRCh38.p7 | 7:43166338 | GTTCCACCTGCCTTG[C/G]CCTCCCAAAGTGCTA | 23072 |
rs535214359 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43529197 | TTCCCACCTCCTCCC[C/G]CTACCATCGCTCCTT | 23072 |
rs535244074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43409487 | AGGGAATGTTTGGAA[A/T]ATCCAGCACTATCAG | 23072 |
rs535249747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43257123 | ACTAAGGGCTGTGGG[G/T]CCACCCGAATGCACA | 23072 |
rs535254429 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43192063 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 23072 |
rs535254523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43474809 | GTTTGTCCTTACAAA[G/T]AAATGAAATTCTGAC | 23072 |
rs535274490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43305895 | CCTCCCAAGTAGCTG[C/G]GATTACAGGCATGTG | 23072 |
rs535275601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153492 | CTTTCTCATGTCTAG[G/T]TTTCCCATCTGGGGA | 23072 |
rs535278128 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43337760 | ATTCCAGCAAATTCT[A/C]AACCTACAGACATTA | 23072 |
rs535288354 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160978 | TCTCCATTTCTACAG[G/T]TTTTTTTTTTCTCCT | 23072 |
rs535289866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43431955 | GCCTCAGCCTCCCAA[C/G]TAGGTGGGATTACAG | 23072 |
rs535292446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522024 | CATTCTGCCATTTGA[C/G]GATACCGCAAGGTGT | 23072 |
rs535316725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119576 | ATTCCAAGTTTATTT[C/T]GTCAGCCCTGACTCA | 23072 |
rs535323797 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43379491 | TCCACTGTCCTCTCC[A/G/T]CTCAATCACTTCCAT | 23072 |
rs535330118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43546157 | GTTAGTTCCTCTGGC[A/G]TGGTGTCTGTCAGCT | 23072 |
rs535336696 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43458198 | AGGCAGAAGTTAGCC[C/T]CTAGGTCTGTCTTGC | 23072 |
rs535343586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43441922 | CTGCTTTAGAATACA[A/G]ACAGTCCGTTCAACT | 23072 |
rs535344734 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43480395 | CTCCTGATCAGTTCC[C/T]GACAATATCATGAGC | 23072 |
rs535347358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43121089 | GCTGGGGTTCTTCCT[A/T]CCTGCCTGGACATTT | 23072 |
rs535351498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43241202 | GCAGATCTGTGTAGC[C/T]GAAGGTGGGCTGCGA | 23072 |
rs535358670 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225233 | TTATTTTACAACCAT[C/T]GAGTTAAAAACAAAG | 23072 |
rs535359995 | snp | G/T | | | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299340 | TTGGTGTATATTTGG[G/T]GCATCTTTGGTGTAT | 23072 |
rs535360694 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43288422 | TTGTAATAAAGCTTT[C/T]CATAATTTTAAGTTG | 23072 |
rs535366892 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43362993 | TTGGCCAGCCCTGGA[A/G]TTCAAATTCTTACCT | 23072 |
rs535380099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43389177 | GACAACTTTAAGATG[C/T]CTATCTTTCCATTAC | 23072 |
rs535388430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43537954 | CTAGGAAACCCCGTC[A/G]CCACACCCCCTGGTT | 23072 |
rs535391010 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43408802 | GGGGAGGCCTAGGTC[A/T]TGAGAGTGGATGGGG | 23072 |
rs535392616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43168412 | CTTGTAATCTCAACA[A/G]TTTGGGAAGCTGAAG | 23072 |
rs535394414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43405619 | GGGTGGTGCTGGTCA[C/T]GTGTGCATCTTCTGC | 23072 |
rs535404599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269811 | ACCTCTGAGGAGACA[A/G]TTGGCAATGTCTGGA | 23072 |
rs535415688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43276873 | CTGAACCATACAGAA[C/T]GCTCTGCAACCCTCC | 23072 |
rs535424432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43172423 | AGAAATCCTAGAGAT[A/T]TCTAGGATTTTTTTT | 23072 |
rs535430191 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43401361 | AAAGGACGAGGGAAA[A/T]AAAGATGAATGGCAC | 23072 |
rs535430613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210253 | TGTCTGTTGTCACTG[C/T]CCAAAACGAACTTAT | 23072 |
rs535434853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43262952 | TATGAACAGTCACAT[A/C]ACATGTCTGTTGAAA | 23072 |
rs535442302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147782 | GGGACTGGCCATTGG[C/T]CACAGTAGTCTTGCC | 23072 |
rs535456162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43276230 | GCAGACTGACTCCTA[A/G]CATAGCCTGTTCTTT | 23072 |
rs535456514 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510169 | ACAAGTCACCGTGGA[A/C]GGGCCCAAGAATGGA | 23072 |
rs535457757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43418660 | TAAGATTGCCATTTG[G/T]TTTTTTTTAATGTGC | 23072 |
rs535460954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43312159 | ATTTTAATAAACTCT[A/G]CAATATAATTAAAAT | 23072 |
rs535510331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296794 | TCAGGGTGCACTTTG[C/T]GGCCTCCACAGCTCT | 23072 |
rs535511407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43264025 | TATGTTTTTATATAC[A/G]TTTATATTGTGGAAT | 23072 |
rs535520756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529311 | ATTCCCTGCACACCC[A/G]ATTCCCTCCCTGCTC | 23072 |
rs535525799 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43403093 | TTATGATGTTGTTGG[C/T]GTGGGAAATAATTTT | 23072 |
rs535526742 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43185528 | GGTAGAGTGTCAGAA[A/T]TGAATCGGAGGACAC | 23072 |
rs535556793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43394486 | TTGGGTGATGTTAAC[C/T]GGGAGAATAAGAGTT | 23072 |
rs535556885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43535421 | CTGTAGTTTTCTTCA[G/T]CGTAGGTCAAGTTCA | 23072 |
rs535557571 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HECW1 | GRCh38.p7 | 7:43360760 | GAGGAGCATCATTGT[C/T]GAGTGTGGCCTGGCT | 23072 |
rs535564696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43208691 | CTCATTGGTGGTTTA[A/G]GTCTAGGACATGCTC | 23072 |
rs535577888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43229881 | AGCTTGTATTGGGTT[A/G]GTGCAAAAGTAATTG | 23072 |
rs535590950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43255635 | TTATTCAATAAATAT[A/G]TATTTTTCAACAGAT | 23072 |
rs535599244 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43363347 | TCAGCAGGTGCCTGA[G/T]TGCTACTGCCCTGAC | 23072 |
rs535614621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43395294 | AAACTACAAACTAAG[C/T]TTCTCCTAAAGTTAG | 23072 |
rs535620447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43355182 | GCTTAAGAGAGTTAT[C/T]TAATCTGAAAAACAA | 23072 |
rs535631859 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43464429 | TTTTCATGGTTTTCA[A/T]TTCTTTGAATTTGCC | 23072 |
rs535641072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43387564 | CTAACAGCAGCAAGA[C/T]ATTTACATAGGAAGC | 23072 |
rs535666689 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43557252 | CAGGTACTGTGAGCC[A/T]CAGTGCATGTGGCCT | 23072 |
rs535667308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43340303 | TCAGCTCACTGCAAC[C/T]GCTGCCTCCCGGGTT | 23072 |
rs535667572 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43400885 | GGTGCAAATCCATCC[C/T]TTGCCACTTTCAGCT | 23072 |
rs535674674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297450 | ACATTGAGACTGTGG[A/G]TGTGTGTGGCCAGTA | 23072 |
rs535676434 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43202630 | AGGCACCTGCCACCA[A/C/T]GCCCAGCTAATTTTT | 23072 |
rs535677844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43537251 | AGAGGGAGCGGCTCC[A/G]CTACTCCTGTAGGGT | 23072 |
rs535678167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43174058 | TTTGGCCAGGCTGAT[A/C]TTGAACTCCTGGCCT | 23072 |
rs535678251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43180938 | AATAGAATAGCTGAA[C/T]TTATTCCTCCTATCT | 23072 |
rs535682245 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242195 | AGGAAGGGCGACATC[A/T]GGTTTCCTTTTTCAA | 23072 |
rs535682838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43529738 | TCTAGGCCCACCAGT[C/T]CCCATCTCCATGCCT | 23072 |
rs535689128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119623 | CTTGAAAATGCAACC[A/G]CCCAGCATCTCCCTT | 23072 |
rs535701833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299246 | ATTTAATGTGAACCT[A/G]TACTACACTGTTGAG | 23072 |
rs535711685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43531137 | TCCTGACTCTTTTCC[A/G]ATGTGATTTTATTTT | 23072 |
rs535723888 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43560068 | CAGAGGAAGAAAACT[A/G]TGAAGATGATGCCTG | 23072 |
rs535725740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43532589 | CTGGCCTCTTTGCAT[C/T]GCTCAAGCAAACCAC | 23072 |
rs535726866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43210844 | GTGGGTCTGCAATGG[C/T]GGTAAATATCAATGG | 23072 |
rs535732008 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43400273 | TAAATTCCATGCCTC[-/A]AAAAAAAGACAAGAC | 23072 |
rs535738049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43236581 | CCAGGTCATAGGTAG[A/G]TAAGAGACAGAAGAT | 23072 |
rs535750138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43388523 | ATCAAACGTGAAGCA[A/G]TGGGTGCTTGGAATG | 23072 |
rs535755723 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43453790 | TCGTGAAGGTACTGT[C/T]TTCAGGTGGCTCTTT | 23072 |
rs535768274 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43196575 | TGCATATGCATGAAT[C/T]TCTTGCCTCATTGAT | 23072 |
rs535772369 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43282964 | CCCTACTAAAAATAC[A/G]TAAGTTAGCTGAGCG | 23072 |
rs535778852 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180338 | GATTTTGAGTAATCA[A/G]ATTGACTTATATTTT | 23072 |
rs535780891 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43425707 | AGAAGCAAGAGACAA[A/G]AGAAAGGAGAACCAG | 23072 |
rs535781636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43306588 | AAGGGCTGTGTATTT[C/T]GCTTACAATTTTTGA | 23072 |
rs535785130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43203089 | GTCTCTTCACACGGA[C/T]GCGCGTGACACTCAG | 23072 |
rs535808036 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43289832 | TACATGGAAGGTGTA[C/T]ACTGGTTAGGCAGGA | 23072 |
rs535810389 | snp | C/T | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111529 | GAAGGGCTGTGCCTC[C/T]TTGCAGAAAAGAGCA | 23072 |
rs535828295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118541 | CTCTTTCCTGTAACA[C/T]ACAGATGAGCTGAAG | 23072 |
rs535830014 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43397417 | GTTCCATCTGTCATG[A/C]ATGTCTGTGTGAAGA | 23072 |
rs535842392 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515402 | GTGGGCAATAGGGGT[-/G]TCATTTAAGAGGCTA | 23072 |
rs535852205 | in-del | -/AT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43423116 | CTGGACAAAGTAAAC[-/AT]AGTGTCATTAGCACA | 23072 |
rs535875031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43253840 | CTGAACCTGGAAGGC[A/G]GAGGTTGCAGTGAGC | 23072 |
rs535880736 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43453227 | AGATTATGTCTTTAT[G/T]CAGGAACCCAGGTGA | 23072 |
rs535883942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43262311 | CTACAAGAAAAAAGA[A/G]AACAATGGCTATAAT | 23072 |
rs535884036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43543555 | AGGCTGAGGTGGGCA[A/G]ATCACCTGAGGTCAG | 23072 |
rs535896740 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268351 | AGTTTAGAGATAGGC[C/T]ACCAAGATTTGAATC | 23072 |
rs535899882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43527732 | TAATAATGCAGTATT[A/G]TGTTTCACTCTGAAC | 23072 |
rs535900864 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43351682 | TTTTCTTTCTTCTTT[C/T]TTTTTTTTTTTTTTT | 23072 |
rs535905806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152674 | CTCTATATTTCCTGT[C/T]AGAAGCTTTCTTCAA | 23072 |
rs535915286 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43426911 | AAAATATATGCAAAA[C/T]GTGGAAGCTGTATCT | 23072 |
rs535918136 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43290536 | GGGAGGGGGTATAAC[A/G]AGGCATGTCTGGCCT | 23072 |
rs535931984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43241007 | GGCTGTGTATAGCTG[C/T]GTGTAAACCAGTTGT | 23072 |
rs535933056 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144258 | CCATTTCATTCCATT[A/G]TATTAACGGTATACA | 23072 |
rs535935153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125941 | GAGACCTTGCTTTCT[A/C]ACCTGGCTTTGTAGT | 23072 |
rs535935312 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43271177 | GAAAACTTAACCAAG[A/G]AACTTTGGGGAAAGA | 23072 |
rs535936812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43371211 | CTTTAATATGATACT[A/G]TGATGGTGGCTACAT | 23072 |
rs535939631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43386800 | GCCAGCTGAAGGGTG[C/T]AGAAGCTAACAGAAG | 23072 |
rs535951255 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HECW1 | GRCh38.p7 | 7:43550316 | AGGAAAAAAGACTCC[A/G]GGGATAATAATGCTG | 23072 |
rs535953088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43166450 | CCAAGCTATAATAGT[A/G]TTAGGATCTAGAAGC | 23072 |
rs535953107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43394021 | GACAAATTTGGGGTG[A/G]ACATTTTTAAATTAG | 23072 |
rs535959975 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43216997 | CCAGAGGGACCAGCT[A/G]TCAAGGGTTCTGTGG | 23072 |
rs535964047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43288243 | ACATGCTGCAGTGAA[A/G]GCTGTAGGTAGTAGA | 23072 |
rs535968164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43385592 | AGGGGCTGATCTCCA[C/T]GAGTTCATGTTGCCC | 23072 |
rs535980074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43471587 | ACCGGGGCAAAGAAC[A/G]CGCTGGCATCTGACT | 23072 |
rs535980454 | in-del | -/AGC | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43122423 | AGGTCATCTGAAAGA[-/AGC]AGCAAGAGTAGAAAT | 23072 |
rs535983285 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43333378 | ACACAGGATTTCAAT[C/T]GCTTCCTCACAGGTA | 23072 |
rs535995797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43338724 | TTTCACGTAAACAGC[A/G]CTCAAATCAAGAAGC | 23072 |
rs536012791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43274677 | AGCGAGAGAGAGCGC[A/G]CAGTAAAATCCTATT | 23072 |
rs536015293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43189551 | TATCATGAAGCTGCT[G/T]CTTCTCATAAAGATA | 23072 |
rs536016898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508601 | ACATACACACACACA[C/T]ATGCATGCACACATT | 23072 |
rs536030661 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348048 | CAGAATGAATTAGAG[A/G]GGGTTCCTTCTTTCT | 23072 |
rs536049594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43249426 | CAACTTCTGAGCCTG[A/C]ACTTTAAGAAGGCGC | 23072 |
rs536052464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, synonymous-codon | HECW1, LOC105375254 | GRCh38.p7 | 7:43113869 | AGAGCCATGATGCGC[G/T]GTGTCTCTGTCTTGC | 23072 |
rs536058221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43339729 | TGGGGTGCTGATGGC[C/T]TTGTCCAATAAGAGG | 23072 |
rs536082199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248898 | ACAACCTCTAGACCC[C/T]AGTGACTTAGGGGCC | 23072 |
rs536086721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43379590 | CTTGCCTGACACTGC[C/T]TCATTCTTTCCACCT | 23072 |
rs536090113 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43545453 | TAAGAATGTGTTGTA[A/G/T]ATCTATAATAATGTA | 23072 |
rs536111155 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157057 | GCAAACCTGGGCTTT[A/G]TGCTAGGCATAGTGG | 23072 |
rs536114762 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43366342 | TGGACAAATAATTGA[C/T]AAATACCCTCCCTTC | 23072 |
rs536117205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154748 | GCTGGAGACATCTCC[C/G]TGCTCTCAAACCTTC | 23072 |
rs536117880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268313 | CAGGGATCCTTACAC[A/G]TGGCTCAGTGGAGAA | 23072 |
rs536123922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43400605 | CTGCTTGTACCCTCA[A/G]CAAAATAGAGGGAAG | 23072 |
rs536125858 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43408068 | TCCAGTTTCTCCACA[A/G]CTCTTCCCATGCATG | 23072 |
rs536149900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43373284 | GCTTGATCTGGGCTC[A/C]CTGCAACCTCTGCCT | 23072 |
rs536151112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43235917 | TGAAGTGCCGGGCAC[A/G]GTGGTTCACACCAGT | 23072 |
rs536162004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43380089 | GACAAGGTCTCACTC[C/T]GTAGCCCAGGCTAGA | 23072 |
rs536169305 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161724 | TTCCAAGGTCTCTGT[A/G]TCACTAAGGTGATTC | 23072 |
rs536176217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154329 | AGGTACAAGTTTGAT[A/G]TGTACTATTAATTTT | 23072 |
rs536179437 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43199462 | AATATTTACATTATT[C/G]TTTTCCCCCTGGAAC | 23072 |
rs536181535 | snp | C/T | | | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510100 | CAAGATGAAACAAAA[C/T]GTGCCCTTTGTTGCC | 23072 |
rs536186375 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124523 | CACGTTGTGAGCACA[C/T]ATCTCCCAGGACCAC | 23072 |
rs536188743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146284 | TTTGTAGGATATTTG[A/G]CAGCATCTCTGGCTT | 23072 |
rs536198713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152924 | CAATTTAGTAATGTC[C/T]GTCACTCCTCTTCTG | 23072 |
rs536212602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43384783 | AGGGAGTGGGTGGCT[A/G]GAAAGAGCTCTATGC | 23072 |
rs536218459 | in-del | -/A | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242402 | AGTGCTTGGTTGGAC[-/A]AAAAGGATGAAGAAA | 23072 |
rs536240905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43338088 | TTCTCTCCACTTAGA[C/T]TGAAACACAGAGACC | 23072 |
rs536248328 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43428966 | AATATATGTATGTGT[A/G]TATGTATGTATACAA | 23072 |
rs536251105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43344683 | TCCTGTGTGTTTCTT[G/T]CTCTTTCGTCTATAT | 23072 |
rs536252847 | snp | C/T | 3.37285e-05 | 0.00410647 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43445236 | CAGCTCCTCGTGCTA[C/T]AGCACGTCCTGCTAC | 23072 |
rs536255957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43200443 | ACAAAATCTGCAAAG[C/T]CAGTCCTCTTCAGCA | 23072 |
rs536260399 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111743 | AGTTCTGAAGTCAGG[C/G]TGAAGCCTTTGTTTA | 23072 |
rs536266764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43329709 | CAGCACACAGTTGCC[C/T]GGACACGGCGTGCTA | 23072 |
rs536268292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550765 | AGTACTGAGGATCTT[C/G]TTGTGGTGGAGGGCT | 23072 |
rs536273886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43422141 | GAGGAAACGTAATTG[C/T]GGTTTTGCCATTAAA | 23072 |
rs536279576 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43232626 | AACATGATGTTCTTG[C/T]GGGAAAAGGGGCAGT | 23072 |
rs536284631 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43534552 | GTGCTTTCTGTCCAT[A/C]TTCCTGGGTAGAGAC | 23072 |
rs536291541 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562180 | AAACAGCTGTCTCAA[A/G]GTCTGTGTATATCTC | 23072 |
rs536299862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521289 | GTTTGCCCACTAGGT[A/G]CAGTAGCACCACCAC | 23072 |
rs536300339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43219657 | AACAGAACAGAACAG[A/T]ACAGAACAGGACAGG | 23072 |
rs536308191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43233871 | ACACAATGGGCATAA[C/T]AGAAGCTGTGATAGC | 23072 |
rs536309853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43457339 | CAAGTATGAAAAGTA[C/T]GAAGGTGAAGGAAAA | 23072 |
rs536314878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144734 | GCACTACAAAATACT[C/T]CAGACTCATCTTGTA | 23072 |
rs536327035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43265957 | GAAACTTGAGGGGGG[A/G]TGTGGATTCTGGAGG | 23072 |
rs536329710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43194732 | GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 23072 |
rs536329842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43552467 | GTCAGTGGCATTTAG[C/T]ACATTCACAGTTTTG | 23072 |
rs536337162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43188228 | GGTTAATGAAAAGTT[A/G]TTTCCAAATCCCACA | 23072 |
rs536347510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43240508 | TTTGTTTTAGCCTAT[A/G]ATAAATCACAGTATG | 23072 |
rs536366292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563496 | GGGAGAAATGTAAGA[C/T]GAAGTGAATTTCATA | 23072 |
rs536367516 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43363741 | CCTTTGTTTGATGGC[A/G]TGGCACACTTTTCAA | 23072 |
rs536373661 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43500978 | CAATTGAGCTAGCAA[C/G]AGCTGCGTAAAGTAC | 23072 |
rs536382189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43287400 | GCAGGAGGAAGAGCC[A/G]GGAGTCCAGGGTTGC | 23072 |
rs536386744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43331119 | TAGGTATATCTCCTG[A/G]TGCTATCCCTCCCCA | 23072 |
rs536400957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43175552 | CCGAGTTAGGAGTTT[C/T]CCTTACGGTGCAGGT | 23072 |
rs536406736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43416918 | ACCCACTGGCCTGCA[A/C]CCACTGCCTGGCACT | 23072 |
rs536411394 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43427387 | TTCACCCTTTTAACC[-/T]AGTACTTCTCTTCAG | 23072 |
rs536420118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43494124 | ACCCTTGCCACTCCC[A/G]CCAGAATGGATCATT | 23072 |
rs536426034 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43299258 | CCTATACTACACTGT[C/T]GAGCAAAGATTCCAC | 23072 |
rs536428977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43226856 | TCATTGGTCAGGGCA[C/G]CCTGCAGAGGATGGC | 23072 |
rs536460956 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43276609 | TAATCCTGATAAAAT[-/G]TGCCTTATTTATTTG | 23072 |
rs536470181 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43174550 | GGACTAGCCCCTGAG[C/T]GAGGTTCTTGTCCCC | 23072 |
rs536470344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43331792 | GGCAGCTTGCCTAAG[C/G]TTCAGAGTGGTAGGT | 23072 |
rs536471705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43424504 | GTTGTGTGCCTGTAG[A/T]TCCAGGTACTCGGGA | 23072 |
rs536475153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43457810 | AAAACATGGAAACAA[A/G]AAAATAAAAATGAAC | 23072 |
rs536479539 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HECW1 | GRCh38.p7 | 7:43322604 | CCTGGTCATGTTGAC[A/C]TCTCCCATTACCTAA | 23072 |
rs536482421 | snp | C/T | | | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513947 | AGGACACAGCCCCTG[C/T]GAGACCTGGCCACAG | 23072 |
rs536485442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43465653 | CAATACAACTGGGTG[A/T]GGATACAAGGAGGAG | 23072 |
rs536496256 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43290331 | AGCCACATGACACCA[A/C]GATAAATTTTAAAAG | 23072 |
rs536499030 | snp | G/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563899 | AAAATAAAAGCATTT[G/T]TTTAGTAGGAATTAT | 23072 |
rs536502816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HECW1 | GRCh38.p7 | 7:43221715 | CCCACCACCACGCCC[A/G]GCTAATTTTTTGTAT | 23072 |
rs536507154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43177439 | TCCCAGGGCAGTCTG[A/G]ACTGAGTTTGTCCCT | 23072 |
rs536509505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213724 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 23072 |
rs536515599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43343819 | TCTAGTTCTAGATCC[C/T]TGAGGAATCCCACAC | 23072 |
rs536518544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43351023 | GGAAGGTCTAGGGCT[A/G]AAGGCTGTTGTTCAG | 23072 |
rs536519419 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43459491 | TAATTTAAGGGAAAT[A/C]GAAGTTTTAAATAGA | 23072 |
rs536526171 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116080 | AATCCTTCACTTTGT[A/G]AGTCAGCTGGGGGAA | 23072 |
rs536555509 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43458971 | AGCAATCAATGTGTA[A/C/T]GCTTGTGTGGTAGGT | 23072 |
rs536560088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43261274 | AAAGAAATTGCCTTT[A/T]TTTCCCCTTAAACAG | 23072 |
rs536567297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43365806 | ATTTGCCAAAGAACA[A/G]AGAACGGCTGGGTGC | 23072 |
rs536587904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43227537 | TAATCTACCAATATG[C/T]CATGTTCTTTCATGA | 23072 |
rs536604184 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43187795 | ATTCTTTTGGTAATT[A/T]TAGGTGAGCTCCAAC | 23072 |
rs536633161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513462 | GCTCCCCTTTGAGAG[C/T]GGGTACTTGACATTC | 23072 |
rs536634830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160269 | AATATTTCCCCCCAA[C/T]TTGTTGTTTGCCTTT | 23072 |
rs536636793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43431813 | CTCTGTGAACTTCAG[C/T]CCCTGCCCATGGCAC | 23072 |
rs536642349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152776 | TTCATTCCGGGGGCC[A/C]TCGGGTCTTCATATC | 23072 |
rs536646561 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43241162 | CTGTCAGGCTGGATC[C/T]CATATGGCAGAAGCA | 23072 |
rs536656215 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43279000 | GCCTAGCATAGTCCC[C/T]GGCTTACAGGAAGTC | 23072 |
rs536663191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43193446 | GAGTGCAATGGTGCA[A/G]TCTTGGCTCACTGCA | 23072 |
rs536666318 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43555016 | GGTATTTGAGCTGTA[A/G]TATCTTGGTCCATGT | 23072 |
rs536680751 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43372117 | GTGAGCCACCAAGCC[C/T]GGCCTCAATATGTTT | 23072 |
rs536681979 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43240559 | TCTAATATTTGGTTT[G/T]TAATCTTAGTTCATT | 23072 |
rs536682772 | snp | A/G | 0.0490535 | 0.14873 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247897 | AAGGGAGGGAGAGAG[A/G]AAGGAAGGAAGGAGG | 23072 |
rs536683756 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43348411 | TTCTCTCTTCTTTTC[G/T]TGGTTAATCTTGCTA | 23072 |
rs536702457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43365881 | AGTGTATCACATGTG[A/G]CCAGGAGTTCAAGAC | 23072 |
rs536704415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43372069 | TCAGGAGATCTGCCC[A/G]TCTCAGCCTCCCAAA | 23072 |
rs536721974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43316859 | CTCCTGTGCCTTCCC[C/G]TAGTGCAGAATCTGG | 23072 |
rs536728725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43273174 | GGTTCTACTAGAAGG[A/G]GGATGGAGGGAGTGG | 23072 |
rs536738288 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43281782 | CAGGCTAGTCTCTTG[C/T]ATTCCTGGCCTCAAG | 23072 |
rs536752974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43234817 | CTGATCCACAGTGCC[C/T]GGTATGAAGTTGGCC | 23072 |
rs536765714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43371884 | GAGTGCAATGGCACG[A/G]TCTCGGCTCACTGCA | 23072 |
rs536768519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153362 | TGTCGATGTATATCC[A/G]TGAACTTTGGGGTAA | 23072 |
rs536771070 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43473160 | CCCACCCTCTACCCC[C/G]ACTCTGTCTGGCTTC | 23072 |
rs536774811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43370709 | ATAAAAAGACATGAG[A/G]AAATCTTAGATGCAT | 23072 |
rs536779625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43412411 | CATTTCCTATTTCTA[A/G]TGCTTTTCATTTCTT | 23072 |
rs536783863 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43332557 | CCTGCAGCCAGGTGG[A/G]TGAGGCAGTGTCTGA | 23072 |
rs536786025 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112443 | CTGGGTGTTGGAAGG[A/G]TGGGGCCGGCGGTAA | 23072 |
rs536798520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43558409 | CTAAGCCCAGACCCA[G/T]GGTGGAGTTGGAGGC | 23072 |
rs536803548 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43326151 | GCCAAAGGGGCTGGG[G/T]TGCCCCTTCAACCTC | 23072 |
rs536813132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43549398 | AGGTACCTGTGTCCA[C/T]AAGTGCCAAACATAT | 23072 |
rs536831331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43502567 | TTCAGGAGGCTAAGG[C/T]GGGATCTCTTGAACC | 23072 |
rs536834963 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43286377 | CTTGATTTTGAGGCT[A/G]GCTTGGGTCCTCAAA | 23072 |
rs536843904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147004 | GGCTGCTTTATGTGG[C/T]AGTGTATTTGCATAC | 23072 |
rs536847871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43507853 | GTTTTGAAAAGTGTG[C/T]TCAGATAATCCCTCG | 23072 |
rs536858435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268446 | GGTGATTTTGTCCCC[C/T]GCGGACATTTGGCAA | 23072 |
rs536880126 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43252907 | TGTTAACCACCAATC[A/G]AACAAGACAAAAGTG | 23072 |
rs536887254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43366483 | TGCTATAGGTTATAA[A/T]ATGTCCTGGAAAATA | 23072 |
rs536891004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43266538 | ACGGAGTTTCACCAT[C/G]TTGGCCAGGCTGGTC | 23072 |
rs536891192 | in-del | -/T | 0.335101 | 0.23507 | intron-variant | HECW1 | GRCh38.p7 | 7:43447168 | TTCTCACTAAAAAGC[-/T]TTTTTTTTTTTGTAT | 23072 |
rs536899896 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43451018 | GTAAACATCTAAAGT[A/C]TTTCCCGACTCCGTG | 23072 |
rs536910210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43206485 | TTTCCTCCCCTCAGT[C/T]CCCCACTAGCTTGGA | 23072 |
rs536931925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123678 | TCTGGCTTGGTGCAC[A/G]TAATTAGCAGGTGGA | 23072 |
rs536950580 | snp | A/G | 0.000232269 | 0.0107741 | intron-variant | HECW1 | GRCh38.p7 | 7:43541313 | TGTCTGCAGGGCAAG[A/G]ACACCGACCTCTCTG | 23072 |
rs536953698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43460251 | GCGGTTCTAGGGGTT[A/T]ATTCTACCAACAGCT | 23072 |
rs536955684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43180102 | AGCAGAGTTGGTAAC[A/G]TTCCCTTTTATGCAA | 23072 |
rs536984118 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140305 | TGCTGAAGTTAGTGG[A/T]CTCACAGGACTAGCA | 23072 |
rs536987139 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HECW1 | GRCh38.p7 | 7:43399518 | TCACTAACCAAAGGT[A/C]CAGTGAAGTCCAAGT | 23072 |
rs536987278 | in-del | -/AAAAT | 0.0809312 | 0.184162 | intron-variant | HECW1 | GRCh38.p7 | 7:43285798 | ATCTCAACAAAAAAT[-/AAAAT]AAAATAAAATAAAAT | 23072 |
rs536988033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43222154 | GTCAGAATTTCTGGG[A/G]TTGGAACCCAGGCTT | 23072 |
rs536991630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43301448 | GTTGACTGCTTAAAT[A/G]TCTGCCTCCTGCACC | 23072 |
rs536991832 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43459589 | GTCGCCCAGGCTGGA[A/G]TGCAGTGGCATTATC | 23072 |
rs536993229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43419738 | CTTGTTTCCCAATGC[C/T]GTAAAGAAATAGCAT | 23072 |
rs536998709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43555824 | GTCTTTGTTGTTTGC[A/G]TGGCTCTACCAATAG | 23072 |
rs537001810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43195338 | CTGTGCCACCTTGTC[A/G]GGCTTCCTAAAGGAG | 23072 |
rs537011549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43405752 | GTTCTGGGAAGGTAG[A/G]AGCCCTCCTGAAATC | 23072 |
rs537015275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43273959 | CGGGTTCAAGCGATT[C/T]TCCTACCTCAGCCTC | 23072 |
rs537038260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43324799 | CCTGGGGATTAAATT[A/T]ACATAATAAAATAAA | 23072 |
rs537047781 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43370990 | CTTCCTGGGTTCTCG[C/T]GATTCTACTGCCTCA | 23072 |
rs537063435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43194849 | CAGGCGCCTGCCCCC[A/T]CACCTGGCTACTTTT | 23072 |
rs537064127 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43191824 | ATACAGCAAACTCAT[A/G/T]TTATGCAGTAGAATA | 23072 |
rs537069278 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43171544 | AGGAGCTCCATGTTC[A/G]CAAACAAGTGGGAAA | 23072 |
rs537071708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521402 | TCACTGTTTTCATGA[C/T]GGAAGACTGGAAAAA | 23072 |
rs537073344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43323964 | TCTTGAACCAGGGAG[G/T]CGGAGGTTGCAGTGA | 23072 |
rs537084401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43378911 | AACAAAATAAAAAAC[C/G]CTTTGCGCTTTGAAC | 23072 |
rs537097004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43457457 | CCAGAAAGAAAAGGA[A/G]GAGAAACAATTTAGT | 23072 |
rs537100812 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43174632 | CTATTTCTCTCCTTC[A/C/G]CACTCAATCTTAGTA | 23072 |
rs537102219 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43220773 | GATAGTAGGTTTAGG[A/G]AAGCCACCAATCCCT | 23072 |
rs537103036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515793 | CCAAAACTTTGTGTC[A/T]TTGGAAACTCTTCAC | 23072 |
rs537118698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213407 | TCAACCTGGAAGAAA[C/T]GGTTTAACACTTAGA | 23072 |
rs537123252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138399 | TTAGTTCCTAAAGCA[C/T]AGATTGCTCCAGCAC | 23072 |
rs537125934 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563940 | CAGCACCCCTTGCAG[C/T]GATGTGTCCGTTGTC | 23072 |
rs537127888 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43111872 | GAATAAATCAGCATT[G/T]TAGAGAATGTGGTTG | 23072 |
rs537136321 | snp | C/T | 0.000399281 | 0.0141238 | missense | HECW1 | GRCh38.p7 | 7:43466483 | TTTCTCCAGTGAACT[C/T]ACAAAAAATCACCTT | 23072 |
rs537136816 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43529030 | GTGTAGAGAATAGAC[A/C]AAACCTACCTAACCC | 23072 |
rs537137424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43260465 | TAGGACACAATATGG[A/T]TTATTGTTTTCATTC | 23072 |
rs537140172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43274707 | TACAAAAATAGACAC[A/G]AACTATCTCTCCATT | 23072 |
rs537149767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43309638 | TATATCCTACTCAAT[C/T]GTAAACCTTACAAAT | 23072 |
rs537177255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HECW1 | GRCh38.p7 | 7:43417018 | TGGGAGCTGTAGACC[A/G]GAGCTGTTCCTATTC | 23072 |
rs537190261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43220300 | GTGTCCTCTCCCTGC[A/G]GGGTCAGGATGCATT | 23072 |
rs537192983 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43477943 | GCTGATATGACTTCA[C/T]CAAATGTTACTGTTG | 23072 |
rs537195673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43550843 | GCTTTCAAGCAACTG[C/G]CATGTGACCCTGGCG | 23072 |
rs537207981 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215698 | TTTGGTAAATGGTCC[A/G]TGGATATTAGAAAAC | 23072 |
rs537208251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43408125 | TTAAATATAGCCTTC[C/T]AGACCAGTTTCAGAG | 23072 |
rs537213339 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119635 | ACCGCCCAGCATCTC[C/T]CTTTGAATGGCACGT | 23072 |
rs537219474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43486757 | GGCACATCACTGTAT[A/G]AACAATATGTAATGA | 23072 |
rs537231283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359955 | ACAGATCTTGTCCTC[C/T]AGGGAACTAAATGCC | 23072 |
rs537232470 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43360731 | AGAAGTCAGACCTGT[C/T]CTTGAGGCCACATGA | 23072 |
rs537232554 | in-del | -/T | 0.0486741 | 0.148216 | intron-variant | HECW1 | GRCh38.p7 | 7:43177118 | GATTTGCATATAAAC[-/T]TTTTTTTTCTATGGC | 23072 |
rs537249277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43139478 | GCTGTGAATCCATTT[C/T]CTACTTAGAGACTCC | 23072 |
rs537251922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43494953 | CCTGCCTTTGTCTTT[C/T]CGGGAATGACTTCCC | 23072 |
rs537255274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43213959 | TTTTTTCAGGAAATT[A/G]AACATTTCATCAGGA | 23072 |
rs537260072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131125 | ACAAAAATTAGATGG[A/G]CGTGGTGGCACACGC | 23072 |
rs537263040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43417730 | CAGTTCCACTGTGTT[A/G]TGGTCTCCATAGTTT | 23072 |
rs537266081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509241 | GATGTTATGAGGGAT[A/G]AGAGTGAATGACAGA | 23072 |
rs537267037 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153361 | CTGTCGATGTATATC[C/T]GTGAACTTTGGGGTA | 23072 |
rs537268976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43318488 | AGTGTTCATTTGCCC[A/C]GTCATTTTTTTGCCA | 23072 |
rs537280340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43452309 | AATCTACTTCGAATC[G/T]GTGCAGTACAGATGA | 23072 |
rs537283585 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43534131 | TTTTATATCACTTTC[A/C/G]TATAAAAGGATTAAC | 23072 |
rs537290009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43178706 | AAAGATGGAAAGAAA[C/T]ATGTCCAAGGTGCCA | 23072 |
rs537303282 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155722 | AGATAATAAAACCTG[A/G]CGAGCATTTATCATG | 23072 |
rs537307469 | in-del | -/T/TT | 0.446961 | 0.247795 | intron-variant | HECW1 | GRCh38.p7 | 7:43191964 | GTTGTTGTTTTTTTC[-/T/TT]TTTTTTTTTTTTGAG | 23072 |
rs537311531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43215402 | AGACGGCAATCCTAC[A/G]TAATGCTATGGATTC | 23072 |
rs537319344 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43336168 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 23072 |
rs537327295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43207551 | TGTAGTCATCTTACC[A/G]TGCTATAGAACCTAG | 23072 |
rs537332385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43551582 | AAATCCAATATTATT[C/T]GAAAACTTCAATGTG | 23072 |