SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs462 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43263084 | TCTTATCTGCATTTT[C/T]CGCAATTACTTACCT | 23072 |
rs463 | snp | C/T | 0.32885 | 0.23724 | intron-variant | HECW1 | GRCh38.p7 | 7:43263185 | GAAACAGGAATTTTA[C/T]TGAAGCATCTAAAAG | 23072 |
rs2292 | snp | C/T | 0.272241 | 0.249009 | intron-variant | HECW1 | GRCh38.p7 | 7:43503054 | TAGCATTCAGAAGTC[C/T]CTCTTAGAGGTAGTT | 23072 |
rs717486 | snp | C/T | 0.188631 | 0.242351 | intron-variant | HECW1 | GRCh38.p7 | 7:43466921 | TAAAATCATTTTCAC[C/T]GATACAATTTCAAAG | 23072 |
rs718809 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43201594 | ATTTGTGACTTAAGG[G/T]ACCCAAGTGGTAAAG | 23072 |
rs721965 | snp | A/G | 0.394171 | 0.204242 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162143 | CAGCTACTTTTTTTC[A/G]TTTCCTTGTGTTTTG | 23072 |
rs728191 | snp | G/T | 0.49306 | 0.0584955 | intron-variant | HECW1 | GRCh38.p7 | 7:43284726 | TCCCTGAAATAATTT[G/T]TATTCTATTCTTAAT | 23072 |
rs736997 | snp | G/T | 0 | 0 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562310 | AAATGTGAGCATTAA[G/T]CACTCCAGGCTTTCA | 23072 |
rs739982 | snp | C/G | 0.49962 | 0.0137727 | intron-variant | HECW1 | GRCh38.p7 | 7:43282329 | CATCACACTCTTTTT[C/G]GCTGACTTCACTCAT | 23072 |
rs740548 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43116325 | TAGAAGGAAACATGG[A/C]CCAAGCACTTTAACC | 23072 |
rs747468 | snp | A/G | 0.0984431 | 0.198823 | intron-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512511 | ATTTAGCTCATCAGC[A/G]TTTTACACatttata | 23072 |
rs749844 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43550855 | TCACGTCTGGCACGC[C/T]AGGGTCACATGCCAG | 23072 |
rs755665 | snp | C/T | 0.418007 | 0.185132 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511849 | TAGGAGAGCCCAGAT[C/T]TGGTGATGTGGCTTT | 23072 |
rs755666 | snp | A/G | 0.452227 | 0.146984 | intron-variant, nc-transcript-variant, utr-variant-3-prime | HECW1, LOC100506895 | GRCh38.p7 | 7:43512048 | CCACAGCGTGGGCGT[A/G]GCTGCTGCTGATCTC | 23072 |
rs757487 | snp | A/G | 0.43978 | 0.162738 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303163 | ACTTCGCTGCTGAAC[A/G]CCTCCAAACATAAAC | 23072 |
rs757488 | snp | A/G | 0.482534 | 0.0918038 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303209 | GAGCTGCACCAAGCA[A/G]TCCTAGACTTGAGCA | 23072 |
rs757489 | snp | C/T | 0.242775 | 0.249896 | intron-variant | HECW1 | GRCh38.p7 | 7:43308977 | AACAAGAAGGGATAT[C/T]ACTGAATAAAATAAT | 23072 |
rs757490 | snp | A/C | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43312918 | TCAACAGATTCAACA[A/C]CGGGTCATCCGAGGC | 23072 |
rs757491 | snp | A/G | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43313147 | CAGCTTGGTTAGTGC[A/G]TTTATAATACACACA | 23072 |
rs757492 | snp | A/G | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43313182 | TGTAAAGATGGAGGT[A/G]CATAAATTGTTGAAA | 23072 |
rs758272 | snp | A/G | 0.4944 | 0.0526182 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142785 | CCCGCTTCTGAGCAT[A/G]AGGCACAGGAAGCTA | 23072 |
rs758916 | snp | G/T | 0.223225 | 0.248562 | intron-variant | HECW1 | GRCh38.p7 | 7:43386604 | AGAAACATGCAGGGG[G/T]GGCAGGAACATCTCC | 23072 |
rs765558 | snp | C/G | 0.462472 | 0.13174 | intron-variant | HECW1 | GRCh38.p7 | 7:43357651 | agtcactctattgat[C/G]tatcaaacactagat | 23072 |
rs765865 | snp | A/G | 0.471673 | 0.115589 | intron-variant | HECW1 | GRCh38.p7 | 7:43386707 | ATCATCTCAAGTTGT[A/G]AGCCCTCATCTCAGG | 23072 |
rs767666 | snp | C/T | 0.287346 | 0.247195 | intron-variant | HECW1 | GRCh38.p7 | 7:43446299 | AAGAAAGAACATCTT[C/T]GGTTAAAACACAGAA | 23072 |
rs767667 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | HECW1 | GRCh38.p7 | 7:43446239 | TGGATTTGATTCTTA[C/T]TGGAAACAAAGTCAT | 23072 |
rs767668 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43446264 | TTTTAAAACTAATGG[G/T]GGCAGCTTTTGGATT | 23072 |
rs769036 | snp | C/G | 0.497445 | 0.0356514 | intron-variant | HECW1 | GRCh38.p7 | 7:43228822 | AATTTATGAAACTAT[C/G]TTAGAATTTTCAATG | 23072 |
rs886439 | snp | G/T | 0.496175 | 0.0435625 | intron-variant | HECW1 | GRCh38.p7 | 7:43220136 | gtaccccttaggttt[G/T]ctaatttactagaat | 23072 |
rs886549 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269574 | GTGAAGGAAGCTGGA[A/G]AGGATGATTGGAGTG | 23072 |
rs886550 | snp | G/T | 0.44546 | 0.155869 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296644 | TAATTCAGGTTTATG[G/T]CTCCTTTGCATCATT | 23072 |
rs886551 | snp | C/T | 0.464523 | 0.128375 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296926 | GGTGACTATACCTCC[C/T]CTTTGCAGCTTTTTG | 23072 |
rs886552 | snp | A/T | 0.44546 | 0.155869 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43297308 | AAATGTCACAATTAC[A/T]CTTGTTTGTTTGTTT | 23072 |
rs917017 | snp | A/G | 0.457037 | 0.140127 | intron-variant | HECW1 | GRCh38.p7 | 7:43325415 | TCAGAATCCTTCCAA[A/G]TCAGGGCTTGGATTG | 23072 |
rs917018 | snp | C/T | 0.390277 | 0.206936 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300882 | GCTGCACACTGTCCC[C/T]GCACCCGCCCAGGAG | 23072 |
rs969023 | snp | C/T | 0.192715 | 0.243348 | intron-variant | HECW1 | GRCh38.p7 | 7:43412105 | gaagtaacgcaaagc[C/T]gtgtacctaaaaatt | 23072 |
rs978056 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | HECW1 | GRCh38.p7 | 7:43339245 | actccaattacatac[A/G]gtggatcattccatt | 23072 |
rs978057 | snp | G/T | 0.17138 | 0.237316 | intron-variant | HECW1 | GRCh38.p7 | 7:43339413 | CATGCATAAAGTTCC[G/T]AATTTCAGCTATTCT | 23072 |
rs1006106 | snp | G/T | 0.453697 | 0.14494 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123456 | AACTTATGTCAAAGC[G/T]CAGGGTCACAGGAGA | 23072 |
rs1006107 | snp | C/T | 0.208169 | 0.246476 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123370 | GGGACCCAAGGTCAA[C/T]GGCAGGTACACTCAG | 23072 |
rs1006108 | snp | A/G | 0.413914 | 0.188765 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43123023 | GCTTTGTCTTTGGAC[A/G]TTTTCACCTTTAACC | 23072 |
rs1015561 | snp | A/T | 0.372995 | 0.217652 | intron-variant | HECW1 | GRCh38.p7 | 7:43340231 | CCCCCCACCCCtttt[A/T]tttttctaagacgga | 23072 |
rs1019971 | snp | A/G | 0.190833 | 0.242898 | intron-variant | HECW1 | GRCh38.p7 | 7:43498698 | ACCTGGGGGGTGTTC[A/G]CAGTGGCTTCTTTGA | 23072 |
rs1025540 | snp | A/C | 0.429388 | 0.174127 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519940 | TCATCTCCTGTGACA[A/C]ATATTGATAATCTAA | 23072 |
rs1025541 | snp | C/T | 0.154993 | 0.231244 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519673 | ggatctgctgtaata[C/T]atttaaccattcccc | 23072 |
rs1029479 | snp | A/G | 0.394721 | 0.203852 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155020 | GGTACAGACTACAAC[A/G]CAAGGCTGCAGCTCA | 23072 |
rs1029480 | snp | A/G | 0.420892 | 0.182472 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43214911 | CAGCTGGGAGGCAGC[A/G]GGTGAGGGGGCCCAT | 23072 |
rs1029481 | snp | A/T | 0.371785 | 0.218331 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43214960 | AGCGTCCCAGGACCC[A/T]GGCCAGGAAGAGCAA | 23072 |
rs1029482 | snp | A/C | 0.386504 | 0.209444 | intron-variant | HECW1 | GRCh38.p7 | 7:43215011 | TGCAAGGTAGCCTAC[A/C]CCTTTTGGGTATTTA | 23072 |
rs1072307 | snp | A/G | 0.465683 | 0.126415 | intron-variant | HECW1 | GRCh38.p7 | 7:43395001 | tgtcttcttgcagtg[A/G]gtcagttcctgggtg | 23072 |
rs1072308 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43394734 | AGGGTTCACCTTGCC[C/G]ACTGTCTAGACAGAG | 23072 |
rs1080173 | snp | C/T | 0.49423 | 0.0534032 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149037 | atacaaaattaccat[C/T]agaacacccctgtaa | 23072 |
rs1080174 | snp | A/C | 0.494358 | 0.0528145 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149240 | caattatcaccagta[A/C]taaaacatattgtca | 23072 |
rs1544418 | snp | C/T | 0.473909 | 0.111197 | intron-variant | HECW1 | GRCh38.p7 | 7:43316135 | TGTTTCTGTAAGCTT[C/T]ATTAGACCTTTCTGA | 23072 |
rs1544419 | snp | A/C | 0.474182 | 0.110646 | intron-variant | HECW1 | GRCh38.p7 | 7:43316287 | TTTTCTGTACATGTT[A/C]TGTACAAAATGTACG | 23072 |
rs1557839 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43214765 | GGGCACGGGCACTAG[C/T]CCAGAAGGAGGAGGA | 23072 |
rs1560856 | snp | C/T | 0.224709 | 0.248717 | intron-variant | HECW1 | GRCh38.p7 | 7:43498558 | CTCTGCCTATGTCCT[C/T]AACCCCAGCCCTGGG | 23072 |
rs1560857 | snp | A/C | 0.424037 | 0.179474 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517159 | TGATTAACAGCATCA[A/C]ATCTGAAATCTGGCC | 23072 |
rs1560858 | snp | C/T | 0.423257 | 0.180228 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517144 | AATCTGAAATCTGGC[C/T]CTGAAAATCCTTCTC | 23072 |
rs1859403 | snp | C/T | 0.442791 | 0.15916 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302503 | GTGGTGCCCTGGTTA[C/T]GGGAAGAGGCACAGT | 23072 |
rs1860754 | snp | G/T | 0.495521 | 0.0471118 | intron-variant | HECW1 | GRCh38.p7 | 7:43434686 | CCCCACCAGGCCCTT[G/T]TCTCCATGCCATGGT | 23072 |
rs1860755 | snp | C/T | 0.16911 | 0.236552 | intron-variant | HECW1 | GRCh38.p7 | 7:43434275 | TCTCCTTTTGACTCT[C/T]TGGTTATTGAACTTT | 23072 |
rs1860756 | snp | C/T | 0.198634 | 0.244666 | intron-variant | HECW1 | GRCh38.p7 | 7:43391457 | GGTATCATTCACTCC[C/T]ACTCCTGCTTACAAA | 23072 |
rs1865317 | snp | C/T | 0.185788 | 0.241613 | intron-variant | HECW1 | GRCh38.p7 | 7:43458215 | GGAGCTTATCATTTT[C/T]GGCAAGACAGACCTA | 23072 |
rs1963417 | snp | A/G | 0.410061 | 0.192043 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519399 | aattagccgggtgtg[A/G]tagtgggcgcctgta | 23072 |
rs1978232 | snp | C/T | 0.493969 | 0.05458 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43133481 | AGATAATTTATTTGT[C/T]TCAACTAGAAATAAA | 23072 |
rs2002505 | snp | A/G | 0.402982 | 0.197728 | intron-variant | HECW1 | GRCh38.p7 | 7:43190153 | GAGTCATGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 23072 |
rs2005721 | snp | A/G | 0.424968 | 0.178567 | intron-variant | HECW1 | GRCh38.p7 | 7:43240313 | ACTACACTCCAGCCT[A/G]GGCGACAGAGCAAGA | 23072 |
rs2017735 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | HECW1 | GRCh38.p7 | 7:43282970 | TAAAAATACATAAGT[G/T]AGCTGAGCGCAGTGG | 23072 |
rs2024125 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118878 | TTTATAAATGTCATA[C/T]ATCACAGTACCATTT | 23072 |
rs2024267 | snp | C/T | 0.486133 | 0.082104 | intron-variant | HECW1 | GRCh38.p7 | 7:43372014 | GCCAACATGGTGAAA[C/T]CCCATCTCTACTAAA | 23072 |
rs2024268 | snp | G/T | 0.367091 | 0.220884 | intron-variant | HECW1 | GRCh38.p7 | 7:43371938 | CAGCTACTAGGGAGG[G/T]TGAGGCAGGAGAATC | 23072 |
rs2024269 | snp | A/C | 0.482083 | 0.0929373 | intron-variant | HECW1 | GRCh38.p7 | 7:43434218 | GGCCCTTAATGGCCA[A/C]TAATCCTATACAGCT | 23072 |
rs2024270 | snp | C/T | 0.297128 | 0.245518 | intron-variant | HECW1 | GRCh38.p7 | 7:43433130 | ATGGAAGTGAATctc[C/T]acccattagatgcca | 23072 |
rs2040761 | snp | C/T | 0.4983 | 0.0291038 | intron-variant | HECW1 | GRCh38.p7 | 7:43189465 | TACAAAAAGAGATTG[C/T]GTGCAGGTCGCTTTG | 23072 |
rs2040840 | snp | A/G | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43234840 | AGTTGGCCCACCACA[A/G]ACATTTGCTGAGTGA | 23072 |
rs2052147 | snp | C/T | 0.0663309 | 0.169604 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359498 | ACAACTGAATAGATT[C/T]ACACATTGCAAATAT | 23072 |
rs2052148 | snp | A/G | 0.493748 | 0.0555599 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359364 | CTAGATACCTACCCG[A/G]CATCCATTCTACCTT | 23072 |
rs2057744 | snp | A/T | 0.49533 | 0.0480965 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150160 | aataaccctattatt[A/T]tcactattttacaga | 23072 |
rs2057745 | snp | A/T | 0.494442 | 0.0524218 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150324 | ACCAATTGATTTCAG[A/T]TAGATTTGCTTTAAC | 23072 |
rs2057746 | snp | G/T | 0.495291 | 0.0482933 | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43150593 | cattctggccaggct[G/T]gttttgaactcctga | 23072 |
rs2057809 | snp | A/G | 0.386694 | 0.20932 | intron-variant | HECW1 | GRCh38.p7 | 7:43326220 | ATATTTTAAAAACAC[A/G]CAGGGGCTCCTGATG | 23072 |
rs2057810 | snp | A/G | 0.493969 | 0.05458 | intron-variant | HECW1 | GRCh38.p7 | 7:43329013 | CCGTCCCTGCATGCC[A/G]AGGTTCTGGCATTAC | 23072 |
rs2079259 | snp | A/T | 0.248471 | 0.249995 | intron-variant | HECW1 | GRCh38.p7 | 7:43342467 | TTTCTCTAAAAGTAC[A/T]GCTCTTATTGTTTCC | 23072 |
rs2079260 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296962 | ACCACCAATTAGAGA[A/C]AGTGATGGCCTCCTT | 23072 |
rs2079261 | snp | A/C | | | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296978 | AGTGATGGCCTCCTT[A/C]TGAGTGcttgcctgc | 23072 |
rs2079262 | snp | C/G | 0.394721 | 0.203852 | intron-variant | HECW1 | GRCh38.p7 | 7:43305885 | cctgcctcagcctcc[C/G]aagtagctgggatta | 23072 |
rs2079263 | snp | A/G | 0.464096 | 0.129085 | intron-variant | HECW1 | GRCh38.p7 | 7:43306417 | TACCCACCTGGTGGC[A/G]TAACAAAGCCGAGTG | 23072 |
rs2079264 | snp | C/T | 0.278664 | 0.248351 | intron-variant | HECW1 | GRCh38.p7 | 7:43231946 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 23072 |
rs2107270 | snp | A/C | 0.368119 | 0.220336 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154173 | ATCTTTCCAAGTAGT[A/C]ATGTGTTTACATGTC | 23072 |
rs2107271 | snp | A/G | 0.47023 | 0.118317 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156688 | AATATTGTACCAGAT[A/G]TTTCTGGTTCTCCAT | 23072 |
rs2107272 | snp | A/G | 0.390277 | 0.206936 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156788 | GTGGAAGTGATGTGT[A/G]TTACCTCTAGGTTGA | 23072 |
rs2107273 | snp | A/G | 0.453209 | 0.145623 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156974 | TATCAGATTAAGTCA[A/G]TGAGATTTGAGGGGC | 23072 |
rs2107274 | snp | G/T | 0.398534 | 0.201091 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157049 | GTTCATTCGCAAACC[G/T]GGGCTTTGTGCTAGG | 23072 |
rs2107554 | snp | A/G | 0.317451 | 0.240729 | intron-variant | HECW1 | GRCh38.p7 | 7:43347702 | aggtatgttccttct[A/G]tgacgattttcctga | 23072 |
rs2107555 | snp | C/T | 0.486332 | 0.08153 | intron-variant | HECW1 | GRCh38.p7 | 7:43347736 | ttttaatcataaatg[C/T]tggattttgtcaaat | 23072 |
rs2109808 | snp | A/T | 0.435407 | 0.167703 | intron-variant | HECW1 | GRCh38.p7 | 7:43405353 | cataccacgagtata[A/T]ctagatgctgagtct | 23072 |
rs2109809 | snp | C/T | 0.257454 | 0.249889 | intron-variant | HECW1 | GRCh38.p7 | 7:43371109 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 23072 |
rs2109810 | snp | C/T | 0.428333 | 0.175206 | intron-variant | HECW1 | GRCh38.p7 | 7:43371045 | aaaaaattagccaga[C/T]gtggtggcgggcacc | 23072 |
rs2109811 | snp | C/G | 0.472241 | 0.114494 | intron-variant | HECW1 | GRCh38.p7 | 7:43370991 | ctgaggcagtagaat[C/G]gcgagaacccaggaa | 23072 |
rs2109812 | snp | G/T | 0.45843 | 0.138046 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360294 | AGCTCAGGACTTTAA[G/T]GCTGCAGAGAGTTAT | 23072 |
rs2117268 | snp | A/T | 0.19646 | 0.2442 | intron-variant | HECW1 | GRCh38.p7 | 7:43454539 | CCTAGGAGATTTTGA[A/T]TAAAATAGATCTAAT | 23072 |
rs2117270 | snp | C/T | 0.45235 | 0.146814 | intron-variant | HECW1 | GRCh38.p7 | 7:43541723 | ACTGATGAATCAGAT[C/T]ATTCAGTCATTTTAG | 23072 |
rs2117271 | snp | C/G | 0.119281 | 0.213102 | intron-variant | HECW1 | GRCh38.p7 | 7:43533477 | ATGCCTCCAGGACAC[C/G]ATTGTAATGTCCTGT | 23072 |
rs2117272 | snp | C/T | 0.395453 | 0.203331 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43519407 | aatacaaaaattagc[C/T]gggtgtgatagtggg | 23072 |
rs2158322 | snp | A/G | 0.175576 | 0.238665 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154353 | TAATTTTTCCTTACT[A/G]GTTAAATATCAGAAG | 23072 |
rs2158465 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43232582 | TGCTTCTGAAGTGTA[G/T]GCTGAAGGCATAGCC | 23072 |
rs2159199 | snp | A/G | 0.483272 | 0.0899109 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43134760 | ACAAAAATGATAGTC[A/G]CAGACAAAACATTAT | 23072 |
rs2159721 | snp | C/G | 0.334412 | 0.235318 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359943 | CCTAGAGGACAAGAT[C/G]TGTAGCCAACATGAG | 23072 |
rs2164038 | snp | C/T | 0.414576 | 0.188188 | intron-variant | HECW1 | GRCh38.p7 | 7:43469889 | GGCTTTGCAGGCCCA[C/T]GTTCACAGAGGAAAG | 23072 |
rs2164039 | snp | A/C | 0.496583 | 0.0411924 | intron-variant | HECW1 | GRCh38.p7 | 7:43454215 | CCTGAGGACACAGAG[A/C]TGAGTGACACATGAC | 23072 |
rs2164040 | snp | A/C | 0.421368 | 0.182025 | intron-variant | HECW1 | GRCh38.p7 | 7:43547892 | CTTTCTTGTTTACTG[A/C]ATATTTTCCACTGTG | 23072 |
rs2164041 | snp | A/G | 0.188 | 0.24219 | intron-variant | HECW1 | GRCh38.p7 | 7:43547524 | GAGTCTCACTCTGTC[A/G]CCAGGCTGGAGTGCA | 23072 |
rs2189451 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155036 | CAAGGCTGCAGCTCA[A/G]GTGACTTAGGGAGCC | 23072 |
rs2189690 | snp | A/G | 0.208169 | 0.246476 | intron-variant | HECW1 | GRCh38.p7 | 7:43331572 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCT | 23072 |
rs2190947 | snp | A/C | 0.383632 | 0.211288 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118369 | AGATTTATGTTTCTC[A/C]AACTGCTCTGACTTG | 23072 |
rs2191825 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43405822 | AGTTAACATAGCAGC[C/T]TGAGACTACTCAACT | 23072 |
rs2196146 | snp | A/T | 0.491629 | 0.0641526 | intron-variant | HECW1 | GRCh38.p7 | 7:43461716 | GAATTACAGAGAGAA[A/T]CATTTGTTGTAATTC | 23072 |
rs2196147 | snp | C/T | 0.490618 | 0.0678448 | intron-variant | HECW1 | GRCh38.p7 | 7:43461606 | TGAGGACTCAGGGAA[C/T]GTAGCCATGGCAGGA | 23072 |
rs2196148 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43458557 | ATTCCTTTTCTTTTT[A/G]TCTGTCCAGATGGAT | 23072 |
rs2196149 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | HECW1 | GRCh38.p7 | 7:43451119 | CACATGGTGAAACTA[C/T]TAGTCAAAAAAACAA | 23072 |
rs2214608 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HECW1 | GRCh38.p7 | 7:43333486 | TACTTATTCCCTACA[A/G]AAAATTTGAGGAAAA | 23072 |
rs2214609 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | HECW1 | GRCh38.p7 | 7:43234123 | ATTACATGCAATACC[A/G]CCCTGCCAGTGACAG | 23072 |
rs2214610 | snp | A/G | 0.452719 | 0.146304 | intron-variant | HECW1 | GRCh38.p7 | 7:43285852 | AATAAATAAATGACA[A/G]TGAGCTAGATAGCAA | 23072 |
rs2215594 | snp | G/T | 0.287346 | 0.247195 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43359016 | CAACATGGTGAAACC[G/T]CATCTCTACTAAAAA | 23072 |
rs2217740 | snp | C/T | 0.49681 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43453871 | CAAAGGAAATAAATT[C/T]GAAATGGAACTTCAG | 23072 |
rs2217741 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | HECW1 | GRCh38.p7 | 7:43453870 | AAAGGAAATAAATTT[A/G]AAATGGAACTTCAGG | 23072 |
rs2240269 | snp | A/G | 0.106987 | 0.205054 | intron-variant | HECW1 | GRCh38.p7 | 7:43250275 | ACTACTCTGAATTCG[A/G]TGACAGACCCTGAAA | 23072 |
rs2240270 | snp | A/G | 0.5 | 0.00019968 | intron-variant | HECW1 | GRCh38.p7 | 7:43252760 | TAAAAGATCCTTGGG[A/G]GCTAAGTCATTTATT | 23072 |
rs2240271 | snp | A/G | 0.105569 | 0.204058 | intron-variant | HECW1 | GRCh38.p7 | 7:43252939 | TTAAGAGCTGACACG[A/G]GAGTCCAGTGGCCAA | 23072 |
rs2240272 | snp | C/T | 0.5 | 0.00019968 | intron-variant | HECW1 | GRCh38.p7 | 7:43253825 | AGGCAGAAGAGTCGC[C/T]TGAACCTGGAAGGCA | 23072 |
rs2240273 | snp | A/G | 0.5 | 0.00019968 | intron-variant | HECW1 | GRCh38.p7 | 7:43254069 | TCTGTGCTGACTGCT[A/G]GTCTTTCTATCTAAA | 23072 |
rs2240983 | snp | C/T | 0.27008 | 0.249192 | intron-variant | HECW1 | GRCh38.p7 | 7:43441038 | AACAAACACATAGCC[C/T]CAAACCAGTTGTTAC | 23072 |
rs2240984 | snp | C/T | 0.315273 | 0.241329 | intron-variant | HECW1 | GRCh38.p7 | 7:43440600 | AGGGCTTTTCTTTTT[C/T]TTGCTTTTCACCCAC | 23072 |
rs2301871 | snp | A/G | 0.461592 | 0.133149 | intron-variant | HECW1 | GRCh38.p7 | 7:43258466 | TTTTTCTAGTGTAGC[A/G]TGCCAATAAAGCGAC | 23072 |
rs2301872 | snp | A/G | 0.255503 | 0.249939 | intron-variant | HECW1 | GRCh38.p7 | 7:43258778 | TTGGTTGGCAAAAAG[A/G]GACATATTTTTATTT | 23072 |
rs2302446 | snp | C/T | 0.177182 | 0.23916 | intron-variant | HECW1 | GRCh38.p7 | 7:43396452 | TGATAGGTCAATAGA[C/T]GTTTACTATTGTAAT | 23072 |
rs2304316 | snp | C/T | 0.480382 | 0.097079 | intron-variant | HECW1 | GRCh38.p7 | 7:43560628 | GCAGCACTCAGGTTA[C/T]GGGGGGAGATTATTT | 23072 |
rs2304317 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | HECW1 | GRCh38.p7 | 7:43560480 | CCTTGGGGAACTATC[C/T]CTAACCCCTACCTCC | 23072 |
rs2304318 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43560441 | TGTCCCTTTCCCCGC[A/T]CAAGCTCCAAAGGCA | 23072 |
rs2304319 | snp | A/G | 0.495559 | 0.0469148 | intron-variant | HECW1 | GRCh38.p7 | 7:43554961 | AATAATATAGTTTCA[A/G]TGCAAGTCTCACAGC | 23072 |
rs2304320 | snp | C/T | 0.0382246 | 0.132858 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43541232 | CTTGTAGAAGGGCCT[C/T]GTGAAGAAAGCGTCA | 23072 |
rs2304321 | snp | A/G | 0.224412 | 0.248687 | intron-variant | HECW1 | GRCh38.p7 | 7:43541029 | TCATTGATGACACAA[A/G]GGAGGCACCTGTTCT | 23072 |
rs2304322 | snp | A/G | 0.318415 | 0.240457 | intron-variant | HECW1 | GRCh38.p7 | 7:43540996 | TCCTTTTGCTTTACC[A/G]TGAACAATCCCTGTG | 23072 |
rs2304323 | snp | A/G | 0.179425 | 0.239831 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43508917 | TGCCCGGAGGTGGGG[A/G]GACCTGTTTGCACCC | 23072 |
rs2304324 | snp | A/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43500883 | GAATCCTCTAGAACA[A/T]GCGGTGAGTTTTTCA | 23072 |
rs2304325 | snp | C/T | 0.401162 | 0.199136 | intron-variant | HECW1 | GRCh38.p7 | 7:43500665 | AAGAGGAAAATTAGA[C/T]GCCAACACATAAACT | 23072 |
rs2304326 | snp | A/G | 0.173965 | 0.238157 | intron-variant | HECW1 | GRCh38.p7 | 7:43479847 | TTAATCTCTTCCAGC[A/G]CAGGCAACCCTAGAT | 23072 |
rs2304327 | snp | A/G | 0.202983 | 0.245539 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43479738 | GAGGGTTACCTCTCC[A/G]GCGCTGTAACTTCGG | 23072 |
rs2304328 | snp | A/G | 0.485394 | 0.0842012 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43466559 | ACTCACATAATTGGC[A/G]TGTAGCACAGTGAAG | 23072 |
rs2304329 | snp | C/T | 0.475893 | 0.107108 | synonymous-codon | HECW1 | GRCh38.p7 | 7:43466460 | TGGAGAAAGTGACCC[C/T]TCTCTCCTTAGATCT | 23072 |
rs2304330 | snp | G/T | 0.485088 | 0.0850877 | intron-variant | HECW1 | GRCh38.p7 | 7:43466416 | GCAAAGCAACAGAAT[G/T]CATTGGGAAAAAGGC | 23072 |
rs2304331 | snp | A/G | 0.307176 | 0.243374 | intron-variant | HECW1 | GRCh38.p7 | 7:43456539 | CCAGTCTCCTCATAC[A/G]GTCTGAGCAGAAAAG | 23072 |
rs2330740 | snp | A/G | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127022 | tacaacagcctttaa[A/G]tgttcaagtggaagg | 23072 |
rs2330741 | snp | A/C | 0.422158 | 0.181278 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127783 | caaacataaaagtac[A/C]agatgaagcaacaag | 23072 |
rs2330742 | snp | A/G | 0.40853 | 0.193309 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127832 | agcaaattgtccaga[A/G]gatccaggtaagatc | 23072 |
rs2330743 | snp | C/T | 0.495291 | 0.0482933 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142977 | TGGCCATGTAACACT[C/T]CAGACTGGAGAGTGG | 23072 |
rs2330744 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, MIR3943, HECW1-IT1 | GRCh38.p7 | 7:43149039 | acaaaattaccatca[A/G]aacacccctgtaata | 23072 |
rs2330745 | snp | C/T | 0.112631 | 0.208878 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155856 | CAACAATCTTACAGG[C/T]GTAACAGCAGATTCG | 23072 |
rs2330784 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | HECW1 | GRCh38.p7 | 7:43229090 | CAGATGTGAGATAGC[C/T]GCTGTACCTTAAGGT | 23072 |
rs2330785 | snp | C/T | 0.342134 | 0.232404 | intron-variant | HECW1 | GRCh38.p7 | 7:43236829 | cttgtgggcacatta[C/T]gagggagttgtgtag | 23072 |
rs2330786 | snp | A/G | 0.457037 | 0.140127 | intron-variant | HECW1 | GRCh38.p7 | 7:43240154 | GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC | 23072 |
rs2330787 | snp | A/G | 0.135143 | 0.222054 | intron-variant | HECW1 | GRCh38.p7 | 7:43313415 | cgatctcagctcacc[A/G]caacctctgcctccc | 23072 |
rs2330788 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | HECW1 | GRCh38.p7 | 7:43342794 | actttgggaggcgca[A/G]gcaggcagatcatga | 23072 |
rs2330789 | snp | A/T | 0.28578 | 0.247426 | intron-variant | HECW1 | GRCh38.p7 | 7:43348098 | caaaagtaccaattc[A/T]tctttcaatgtctgg | 23072 |
rs2330790 | snp | A/T | 0.209736 | 0.246736 | intron-variant | HECW1 | GRCh38.p7 | 7:43348169 | ttgtttgtaattttt[A/T]aattaccattttaat | 23072 |
rs2330791 | snp | A/C | 0.477684 | 0.103247 | intron-variant | HECW1 | GRCh38.p7 | 7:43354004 | atagtcctgggataa[A/C]ccttttgggacctcc | 23072 |
rs2330792 | snp | C/T | 0.35207 | 0.228214 | intron-variant | HECW1 | GRCh38.p7 | 7:43357513 | tgggagctaacaaag[C/T]ggatctcatggagat | 23072 |
rs2330868 | snp | G/T | 0.196149 | 0.244131 | intron-variant | HECW1 | GRCh38.p7 | 7:43421117 | gctaattaaatagat[G/T]agaatccagaaatag | 23072 |
rs2330869 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HECW1 | GRCh38.p7 | 7:43432821 | TACCCTGTTTTAATT[C/T]CATTAAGTTCAATTT | 23072 |
rs2330870 | snp | C/G | 0.475348 | 0.108251 | intron-variant | HECW1 | GRCh38.p7 | 7:43443682 | TCTAAATGTTGGGAA[C/G]CTTCCAGCCTGAGAT | 23072 |
rs2330872 | snp | C/T | 0.496616 | 0.0409947 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518698 | CCCTGGGAAAACTGG[C/T]AAAGAATATGAAAAA | 23072 |
rs2330873 | snp | C/T | 0.188946 | 0.24243 | intron-variant | HECW1 | GRCh38.p7 | 7:43532063 | AATAGGCAGCACAAA[C/T]GTAATATGTCTGAAA | 23072 |
rs2330874 | snp | C/T | 0.33303 | 0.235809 | intron-variant | HECW1 | GRCh38.p7 | 7:43545811 | gaaggtttggtcttg[C/T]tgtctcggggtggag | 23072 |
rs2877205 | snp | A/G | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154847 | TTTCTGGAAAGGTTA[A/G]GCATTATCTTTTTGT | 23072 |
rs3032876 | in-del | -/CTC | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248690 | ctcctcctcctcctc[-/CTC]cttttcctcctcctc | 23072 |
rs3032877 | in-del | -/CTCCTC | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248717 | ctcctcctcctcctc[-/CTCCTC]ctccttttcctcctc | 23072 |
rs3032878 | in-del | -/T/TT/TTT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43313354 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GAGATGGAGTTTTGC | 23072 |
rs3032881 | in-del | -/GTGTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43317852 | tgtgtgtgtgtgtgt[-/GTGTGT]tTGCCATCCTCGTCA | 23072 |
rs3032902 | in-del | -/CTC | 0.28052 | 0.24813 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43358932 | CGGGTTCCAGCAATT[-/CTC]CTGCTTCAGCCTTCC | 23072 |
rs3032904 | in-del | -/TGTGTG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361079 | gtgtgtgtgtgtgtg[-/TGTGTG]tgtgtacgtgtACAT | 23072 |
rs3037055 | in-del | -/CA | 0.0652144 | 0.168387 | intron-variant | HECW1 | GRCh38.p7 | 7:43437350 | ttttgggtttttctc[-/CA]gtcttttactattgt | 23072 |
rs3037087 | in-del | -/AG | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488411 | AAGGAAATGAAAGAA[-/AG]AGAGAGAGAGAAAGA | 23072 |
rs3037095 | in-del | -/AAA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43546627 | atatcaaaaaaaaaa[-/AAA]caaacaaactttaaa | 23072 |
rs3138780 | microsatellite | (CA)20/21/22/24/25/26/27 | | | intron-variant | HECW1 | GRCh38.p7 | 7:43241613 | ATCCAATTAATTAAA[(CA)20/21/22/24/25/26/27]TTAGGAGAGTAAAAA | 23072 |
rs3214213 | in-del | -/T | 0.332106 | 0.236133 | intron-variant | HECW1 | GRCh38.p7 | 7:43250104 | TTCCTCTCTTGCAGA[-/T]TTTTTTTAACCAAAA | 23072 |
rs3214630 | in-del | -/AACTT | 0.256897 | 0.249905 | intron-variant | HECW1 | GRCh38.p7 | 7:43456633 | ATGACACTCAAGCTT[-/AACTT]GTCTCTCGCCTCCAA | 23072 |
rs3214631 | in-del | -/A | 0.473348 | 0.112319 | intron-variant | HECW1 | GRCh38.p7 | 7:43456279 | AGTGTTTAATAAAAA[-/A]GGCAAAAAGAAAAAT | 23072 |
rs3216963 | in-del | -/CACA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250158 | acacatacacacaca[-/CACA]GAAATACAAAATAAA | 23072 |
rs3221268 | microsatellite | (CA)20/21/22/24/25/26/27 | 0.737112 | 0.138232 | intron-variant | HECW1 | GRCh38.p7 | 7:43241617 | NTCCAATTAATTAAA[(CA)20/21/22/24/25/26/27]ATTAGGAGAGTAAAA | 23072 |
rs3735072 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43562472 | TGTATAAAAATTTCA[C/G]CTTTGCCACTGTTGT | 23072 |
rs3735074 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HECW1 | GRCh38.p7 | 7:43451059 | TTAGAGCAGGTGTCA[C/T]ATTGGTCTTTGTTAA | 23072 |
rs3735075 | snp | A/G | 0.347914 | 0.230028 | intron-variant | HECW1 | GRCh38.p7 | 7:43440076 | CCTAACCACGGTGGG[A/G]CACCTCCGGAGGAGG | 23072 |
rs3757564 | snp | C/T | 0.239902 | 0.249796 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43163063 | AAACAACCCGGCACC[C/T]TTGGACCTGTGCAGG | 23072 |
rs3801397 | snp | A/C | 0.494774 | 0.0508504 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511240 | TCCACTGATGTTCTC[A/C]CTCATGTGGAGAGTA | 23072 |
rs3816072 | snp | C/T | 0.254181 | 0.249965 | intron-variant | HECW1 | GRCh38.p7 | 7:43541305 | TCGGTGTCCTTGCCC[C/T]GCAGACAGGGCTGGG | 23072 |
rs3823863 | snp | A/G | 0.268452 | 0.249318 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43511413 | ATGATTTAAAGCTGC[A/G]ACTCTGAATGCCTCA | 23072 |
rs3857751 | snp | C/T | 0.484632 | 0.086302 | intron-variant | HECW1 | GRCh38.p7 | 7:43479241 | GCCATCTGGGGGTAA[C/T]GAGAGACGGTGACAG | 23072 |
rs3886967 | snp | A/G | 0.499846 | 0.00878459 | intron-variant | HECW1 | GRCh38.p7 | 7:43334516 | AAACAACCCTTATCC[A/G]TTGCAGCAGCTACTA | 23072 |
rs3886968 | snp | C/T | 0.175576 | 0.238665 | intron-variant | HECW1 | GRCh38.p7 | 7:43334517 | AACAACCCTTATCCG[C/T]TGCAGCAGCTACTAA | 23072 |
rs3919666 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43461488 | TACTGGGAGGATTCC[C/T]TAAATGCTTtatggc | 23072 |
rs3940512 | snp | C/T | 0.185788 | 0.241613 | intron-variant | HECW1 | GRCh38.p7 | 7:43458022 | TTCCTCTCTGTAACA[C/T]GCTTTGTTGGGGTGA | 23072 |
rs3944045 | snp | A/T | 0.483636 | 0.0889627 | intron-variant | HECW1 | GRCh38.p7 | 7:43370884 | aaaaaaaaaaagaat[A/T]tcattgccctaaaaa | 23072 |
rs4049927 | in-del | -/TAT | 0.273587 | 0.248885 | intron-variant | HECW1 | GRCh38.p7 | 7:43327962 | TCTATGAACCATTTA[-/TAT]TATTATTATTATTAT | 23072 |
rs4140829 | snp | C/G | 0.497907 | 0.0322805 | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112127 | CTAGCTCCCAAACCG[C/G]GTTTTCTATTACACT | 23072 |
rs4304246 | snp | A/G | 0.489318 | 0.0722982 | intron-variant | HECW1 | GRCh38.p7 | 7:43242732 | GGACCTTCTCCAAGG[A/G]GGAAGGCAGTGCAGG | 23072 |
rs4324849 | snp | C/T | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43128394 | agaattatgctaaat[C/T]tattttgcctgtgct | 23072 |
rs4373425 | snp | C/G | 0.283421 | 0.247756 | intron-variant | HECW1 | GRCh38.p7 | 7:43535202 | AAACAGCAATGCGCT[C/G]AAGGGGAGGGTTGAG | 23072 |
rs4421275 | snp | A/G | 0.361263 | 0.223876 | intron-variant | HECW1 | GRCh38.p7 | 7:43347103 | ggtcattttcacaat[A/G]ttgattctacccatc | 23072 |
rs4433042 | snp | A/G | 0.441841 | 0.160303 | intron-variant | HECW1 | GRCh38.p7 | 7:43483085 | GGTCTGAGCCAAGCA[A/G]CAGGTTCCCGCTTGC | 23072 |
rs4437556 | snp | C/T | 0.400325 | 0.199756 | intron-variant | HECW1 | GRCh38.p7 | 7:43189815 | AACTTTAAGTAGATA[C/T]GTCTCATAAAATGTC | 23072 |
rs4457234 | snp | A/G | 0.188316 | 0.242271 | intron-variant | HECW1 | GRCh38.p7 | 7:43540605 | TTTATGTGGCTGGCA[A/G]TTTTAAAGAGTGATG | 23072 |
rs4460277 | snp | C/T | 0.336702 | 0.234484 | intron-variant | HECW1 | GRCh38.p7 | 7:43228871 | TGGAATATAAAATTG[C/T]GTATACAATATGTCT | 23072 |
rs4509217 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | HECW1 | GRCh38.p7 | 7:43321409 | GGTCCCCATACTGGT[A/G]TATTTCTCATTGCAT | 23072 |
rs4534059 | snp | G/T | 0.123798 | 0.215808 | intron-variant | HECW1 | GRCh38.p7 | 7:43535224 | AGGGTTGAGTCTTTT[G/T]GGGGCCTTTAAGCCA | 23072 |
rs4570049 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | HECW1 | GRCh38.p7 | 7:43535198 | CAACAAACAGCAATG[C/T]GCTGAAGGGGAGGGT | 23072 |
rs4591931 | snp | A/C | 0.0803491 | 0.183626 | intron-variant | HECW1 | GRCh38.p7 | 7:43347920 | gttggattcatttag[A/C]tactattttgttaaa | 23072 |
rs4612244 | snp | A/G | 0.480853 | 0.0959518 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119026 | ATATTTTATTGTGAC[A/G]TATTTGATTTTGACA | 23072 |
rs4623323 | snp | A/C | 0.474091 | 0.11083 | intron-variant | HECW1 | GRCh38.p7 | 7:43241854 | AAAAATAATAACTAC[A/C]GGGTACTATTCCCAG | 23072 |
rs4636109 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156069 | CACTTAACTGGGGGA[A/G]ATAAATTCTACCAAT | 23072 |
rs4720443 | snp | C/T | 0.046775 | 0.145601 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132019 | CCCAGTTTAGTGAAA[C/T]CTCTGTTGTTAGGTT | 23072 |
rs4720444 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | HECW1 | GRCh38.p7 | 7:43176156 | TGGTAAATAATGGCA[A/G]ACATTTGTACCCCTG | 23072 |
rs4720447 | snp | A/G | 0.118933 | 0.212888 | intron-variant | HECW1 | GRCh38.p7 | 7:43532729 | TTGACACTCCCTGGC[A/G]CATTCAGAAGGAATT | 23072 |
rs4720448 | snp | A/C | 0.498982 | 0.0225409 | intron-variant | HECW1 | GRCh38.p7 | 7:43532755 | GAATTATTCTCCCCC[A/C]TCATCACTTCCCCAA | 23072 |
rs4720449 | snp | A/G | 0.321292 | 0.23962 | intron-variant | HECW1 | GRCh38.p7 | 7:43540125 | AAATATATTTATTCT[A/G]TGGAATCAGATAATC | 23072 |
rs4720450 | snp | C/T | 0.499609 | 0.0139722 | intron-variant | HECW1 | GRCh38.p7 | 7:43555801 | TCAGCAGACCCTCAG[C/T]TCCAAGGGTCTTTGT | 23072 |
rs4724177 | snp | G/T | 0.414245 | 0.188477 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124108 | TGACTCCGTCCTTTT[G/T]CAAGTGTTCATTTGT | 23072 |
rs4724180 | snp | A/G | 0.383439 | 0.21141 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132688 | gtgagtgccttttAT[A/G]TTATCTCTAACACAA | 23072 |
rs4724183 | snp | C/T | 0.188946 | 0.24243 | intron-variant | HECW1 | GRCh38.p7 | 7:43187667 | CTTTTCTATATTAAC[C/T]GTGATAATCTTTAAA | 23072 |
rs4724184 | snp | A/G | 0.217551 | 0.247885 | intron-variant | HECW1 | GRCh38.p7 | 7:43195699 | AAATCATGAAAGTTG[A/G]GAGATTTATTTGCAA | 23072 |
rs4724185 | snp | A/G | 0.404035 | 0.196909 | intron-variant | HECW1 | GRCh38.p7 | 7:43200881 | ATAGCTACAAAGCCA[A/G]CAAGATGGGAAACCT | 23072 |
rs4724193 | snp | A/G | 0.499974 | 0.00359416 | intron-variant | HECW1 | GRCh38.p7 | 7:43266091 | atgattgattaaatc[A/G]ctggccattgattgt | 23072 |
rs4724194 | snp | A/G | 0.499 | 0.0223418 | intron-variant | HECW1 | GRCh38.p7 | 7:43266517 | ttttttgtattttta[A/G]tagagacggagtttc | 23072 |
rs4724195 | snp | C/T | 0.494484 | 0.0522255 | intron-variant | HECW1 | GRCh38.p7 | 7:43286598 | ATTTTTTCTTTACTA[C/T]TTCTATTGGCAAATG | 23072 |
rs4724197 | snp | A/G | 0.456568 | 0.140818 | intron-variant | HECW1 | GRCh38.p7 | 7:43325182 | CTATTTGACCATAGT[A/G]TCAATGGCTATAACA | 23072 |
rs4724202 | snp | A/C | 0.406986 | 0.194565 | intron-variant | HECW1 | GRCh38.p7 | 7:43410033 | AGTGAGCCCCCAGGG[A/C]TCCCAGCTCTCCGGG | 23072 |
rs4724203 | snp | G/T | 0.437965 | 0.164831 | intron-variant | HECW1 | GRCh38.p7 | 7:43412111 | taggtacacggcttt[G/T]cgttacttcctttgt | 23072 |
rs4724204 | snp | C/G | 0.458084 | 0.138567 | intron-variant | HECW1 | GRCh38.p7 | 7:43412660 | ttcctgtgtccatgt[C/G]atctcaatgttcaat | 23072 |
rs4724205 | snp | A/C | 0.405255 | 0.195948 | intron-variant | HECW1 | GRCh38.p7 | 7:43423718 | GACAGCTCATGTGCA[A/C]CTCTTCCCAACTCCA | 23072 |
rs4724206 | snp | A/G | 0.310386 | 0.242597 | intron-variant | HECW1 | GRCh38.p7 | 7:43450538 | TTCCTTTCTGGTGCC[A/G]CTTTCTGATTCAGGA | 23072 |
rs4724207 | snp | C/G | 0.494774 | 0.0508504 | intron-variant | HECW1 | GRCh38.p7 | 7:43451397 | TCCTTACTATAACTT[C/G]CATCCATAGGGAATA | 23072 |
rs4724208 | snp | A/G | 0.485324 | 0.0843964 | intron-variant | HECW1 | GRCh38.p7 | 7:43455527 | CTTAGCAAAGAAAGC[A/G]TTCTCCAGCATCACA | 23072 |
rs4724209 | snp | A/G | 0.485324 | 0.0843964 | intron-variant | HECW1 | GRCh38.p7 | 7:43455686 | ATTATTAGAATTTTT[A/G]TATTCGTCACACCAT | 23072 |
rs4724210 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | HECW1 | GRCh38.p7 | 7:43531342 | cttcaccacttgctc[C/T]gtggtgatgagatac | 23072 |
rs4724211 | snp | C/T | 0.118933 | 0.212888 | intron-variant | HECW1 | GRCh38.p7 | 7:43532728 | GTTGACACTCCCTGG[C/T]ACATTCAGAAGGAAT | 23072 |
rs4724212 | snp | C/T | 0.119281 | 0.213102 | intron-variant | HECW1 | GRCh38.p7 | 7:43533148 | TGGGCATCTAGTAGG[C/T]AGGAGTCAGAGATGC | 23072 |
rs4724213 | snp | C/T | 0.284733 | 0.247575 | intron-variant | HECW1 | GRCh38.p7 | 7:43535978 | AGGATATGAAAATAA[C/T]TTATATCAGAGTCCA | 23072 |
rs4724214 | snp | A/G | 0.123798 | 0.215808 | intron-variant | HECW1 | GRCh38.p7 | 7:43536016 | TCCCACAAACCACAG[A/G]GTTGTGGTTTGGATT | 23072 |
rs4724215 | snp | C/T | 0.124144 | 0.21601 | intron-variant | HECW1 | GRCh38.p7 | 7:43536406 | CATTCCTGACCCATC[C/T]GGGTGTGGCTAGAAT | 23072 |
rs4724216 | snp | C/G | 0.350201 | 0.247216 | intron-variant | HECW1 | GRCh38.p7 | 7:43537997 | ACAGTGATCCCACCC[C/G]CTGGTTGAGAGTGGT | 23072 |
rs4724217 | snp | A/T | 0.32153 | 0.239548 | intron-variant | HECW1 | GRCh38.p7 | 7:43541416 | GTGCTTAGATATCAC[A/T]TACATTTTTTAGCAC | 23072 |
rs4724218 | snp | A/C | 0.420892 | 0.182472 | intron-variant | HECW1 | GRCh38.p7 | 7:43548378 | CCATGTACGAGTGGA[A/C]CCATGCAGTCCAAAC | 23072 |
rs4724219 | snp | G/T | 0.312104 | 0.242163 | intron-variant | HECW1 | GRCh38.p7 | 7:43549349 | GTGATAAAAGAAAAA[G/T]TCACCATCAGACTAC | 23072 |
rs4724220 | snp | A/G | 0.499875 | 0.00789017 | intron-variant | HECW1 | GRCh38.p7 | 7:43552356 | GTGGGCAGGAGCTGT[A/G]ATGATGCAATGATCA | 23072 |
rs4724221 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | HECW1 | GRCh38.p7 | 7:43554330 | TCTCAGTTGTTTAAA[C/T]AGAAAGCAGACATCT | 23072 |
rs4724222 | snp | A/G | 0.040671 | 0.13668 | intron-variant | HECW1 | GRCh38.p7 | 7:43555467 | AAGAGACAGTTGTGC[A/G]TAGGCGCTATAGTGA | 23072 |
rs4724223 | snp | A/G | 0.040671 | 0.13668 | intron-variant | HECW1 | GRCh38.p7 | 7:43555895 | AAAAAGGCAGAATTT[A/G]CATTTGTTAAGTTGA | 23072 |
rs4724224 | snp | A/G | 0.040671 | 0.13668 | intron-variant | HECW1 | GRCh38.p7 | 7:43560163 | TTCGCCTGTTTAGCC[A/G]TAGCCCAATGTATGT | 23072 |
rs5883857 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114731 | GGAATGACAGTTCTC[-/T]TTTTTTTTTGGAGTA | 23072 |
rs5883858 | in-del | -/A | 0.301681 | 0.2446 | intron-variant | HECW1 | GRCh38.p7 | 7:43246852 | GGCAGAGCCTCTGCC[-/A]AGCCCAGTGGACTCT | 23072 |
rs5883860 | in-del | -/A | 0.494692 | 0.0512434 | intron-variant | HECW1 | GRCh38.p7 | 7:43323872 | AACCCCATCTCTGCT[-/A]AAAATACAAAAATTA | 23072 |
rs5883861 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43324041 | ctctatctcaaaaaa[A/G]aaaaaaaaaGGCTTG | 23072 |
rs5883862 | in-del | -/A | 0.497359 | 0.0362457 | intron-variant | HECW1 | GRCh38.p7 | 7:43324041 | AAAAAGAAAAAAAAA[-/A]GGCTTGCAGAAGGCA | 23072 |
rs5883864 | in-del | -/T | 0.450483 | 0.149354 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43360215 | ATTTATAGAACTTTC[-/T]TTTTTTTTTTTTTTT | 23072 |
rs5883866 | in-del | -/A | 0.144654 | 0.226721 | intron-variant | HECW1 | GRCh38.p7 | 7:43434042 | TTTTTTAAAAAAAAA[-/A]CAAAAAACCTTTTGC | 23072 |
rs5883869 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494507 | GAAATAAAGTCAAGA[-/T]TTTTTTTTTTTTTTG | 23072 |
rs5883870 | in-del | -/A | 0.306632 | 0.244621 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524007 | TATGTTTTTCATCTT[-/A]AAAAAAAAAGATGAG | 23072 |
rs5883871 | in-del | -/A | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43550105 | AGACCACATTCTACC[-/A]AAAAAAAAAGAAGAA | 23072 |
rs6415276 | snp | C/G | 0.460365 | 0.13508 | intron-variant | HECW1 | GRCh38.p7 | 7:43409575 | TGAAGCTTTGGTTAA[C/G]ACTGATTTTGTTCTG | 23072 |
rs6463165 | snp | A/G | 0.0566069 | 0.158427 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118440 | GGGGGAAAAGATGGG[A/G]AGAATAAAATTAAAC | 23072 |
rs6463166 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43146832 | TGCACAGACAGCTCA[C/T]GGCCCATTAGTGTAT | 23072 |
rs6463167 | snp | A/G | 0.495252 | 0.0484902 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147107 | CTATTAAAGTTGTCT[A/G]TTATCCAAGGAAACC | 23072 |
rs6463169 | snp | C/T | 0.39709 | 0.20215 | intron-variant | HECW1 | GRCh38.p7 | 7:43168054 | ATAGCCCGTGGTGTA[C/T]GCTTCCTTTCGGCAT | 23072 |
rs6463170 | snp | C/T | 0.447809 | 0.152878 | intron-variant | HECW1 | GRCh38.p7 | 7:43168263 | TATGTTCAGCCTGTG[C/T]GAGAGACAGAGAGAG | 23072 |
rs6463171 | snp | C/T | 0.306679 | 0.24349 | intron-variant | HECW1 | GRCh38.p7 | 7:43183692 | actatccatagtcaa[C/T]ctatggttacaactg | 23072 |
rs6463172 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43183881 | tttttgctatttaca[A/G]tataacaagtgtagg | 23072 |
rs6463173 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43186777 | gcattacaattgcct[A/G]cagtattcagaacag | 23072 |
rs6463174 | snp | A/C | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43186846 | tcatataggttatat[A/C]atacagcctaggtgt | 23072 |
rs6463175 | snp | A/C | 0.296619 | 0.245615 | intron-variant | HECW1 | GRCh38.p7 | 7:43186963 | tattaagtgacatga[A/C]tgTATTGATGatttt | 23072 |
rs6463176 | snp | G/T | 0.244695 | 0.249944 | intron-variant | HECW1 | GRCh38.p7 | 7:43190086 | ACAGCTGTGGAAATT[G/T]TTGTTGTTGTTGTTG | 23072 |
rs6463177 | snp | C/G | 0.455024 | 0.143057 | intron-variant | HECW1 | GRCh38.p7 | 7:43206290 | CGGAGTCAAGAGGAT[C/G]TTCCGGGAGGCTCTG | 23072 |
rs6463178 | snp | A/G | 0.103438 | 0.202533 | intron-variant | HECW1 | GRCh38.p7 | 7:43250197 | ATTTGGTAGCATTGT[A/G]TTTGTCTTAAAATTC | 23072 |
rs6463179 | snp | C/T | 0.480144 | 0.097642 | intron-variant | HECW1 | GRCh38.p7 | 7:43309419 | ATGTTTCCTTCTCTA[C/T]CTTTGCTCTCACCAT | 23072 |
rs6463180 | snp | A/G | 0.497722 | 0.0336691 | intron-variant | HECW1 | GRCh38.p7 | 7:43310590 | ACTCAGAATGCCAAC[A/G]CTGTGCTTTCTCAGG | 23072 |
rs6463181 | snp | A/G | 0.474992 | 0.108989 | intron-variant | HECW1 | GRCh38.p7 | 7:43313807 | cagctggagttaagc[A/G]tctgcaccctcccta | 23072 |
rs6463182 | snp | A/C | 0.279726 | 0.248226 | intron-variant | HECW1 | GRCh38.p7 | 7:43317944 | TTGATAATTAACCCC[A/C]TTTTGTACATTCTAT | 23072 |
rs6463183 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | HECW1 | GRCh38.p7 | 7:43333278 | TTAGTATACAGTCTT[C/T]CTCATATCCAGATGA | 23072 |
rs6463185 | snp | A/C | 0.318896 | 0.240319 | intron-variant | HECW1 | GRCh38.p7 | 7:43350287 | gcttctatctcacag[A/C]ccttaagattctttc | 23072 |
rs6463186 | snp | C/T | 0.471768 | 0.115407 | intron-variant | HECW1 | GRCh38.p7 | 7:43380675 | gggattacaggcacc[C/T]accaccacactcggg | 23072 |
rs6463187 | snp | C/T | 0.471578 | 0.115772 | intron-variant | HECW1 | GRCh38.p7 | 7:43380995 | gttccacatccttgc[C/T]aacacttgatattgt | 23072 |
rs6463188 | snp | C/T | 0.482309 | 0.0923707 | intron-variant | HECW1 | GRCh38.p7 | 7:43381007 | tgctaacacttgata[C/T]tgtctttttattttt | 23072 |
rs6463190 | snp | A/G | 0.461037 | 0.134028 | intron-variant | HECW1 | GRCh38.p7 | 7:43419262 | agtgactgtggcggc[A/G]ttcagggcaaagatc | 23072 |
rs6463191 | snp | A/G | 0.45946 | 0.136478 | intron-variant | HECW1 | GRCh38.p7 | 7:43452580 | atttattgaatgttt[A/G]ccctgtgctaggtac | 23072 |
rs6463192 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | HECW1 | GRCh38.p7 | 7:43460533 | Ttgtacgtgtgtgtg[C/T]gcgcgtgcgtgtgtg | 23072 |
rs6463193 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | HECW1 | GRCh38.p7 | 7:43480150 | CCTAGAAAATACTTC[A/G]ATAATGTATCCATGG | 23072 |
rs6463194 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43484847 | ATATTCAAGCACCAG[A/C]AAAGCAGGCCTTATC | 23072 |
rs6463195 | snp | A/G | 0.41833 | 0.184838 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516040 | AAGGGTCTTTCCTGA[A/G]CACTCAATTTAAAAT | 23072 |
rs6463196 | snp | C/T | 0.418007 | 0.185132 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516602 | TAAAAGTCTGAACAA[C/T]TGAAATAGGTGAGTT | 23072 |
rs6463197 | snp | A/C | 0.489201 | 0.0726845 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520555 | AATACTGTGTAGTTC[A/C]TTCATGATTTCTTCA | 23072 |
rs6942969 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HECW1 | GRCh38.p7 | 7:43276417 | GTTTCTCACACAGTC[A/G]TTTGTAGAATTTAAA | 23072 |
rs6943005 | snp | C/G | 0.368938 | 0.219895 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153697 | CTTAGTTGTCCAGAC[C/G]TCATTTTCCTGAGGT | 23072 |
rs6943440 | snp | A/G | 0.461148 | 0.133852 | intron-variant | HECW1 | GRCh38.p7 | 7:43211705 | CCTCCCTCAAATTTT[A/G]CCTGTGCATTACCCA | 23072 |
rs6943501 | snp | C/T | 0.344815 | 0.231323 | intron-variant | HECW1 | GRCh38.p7 | 7:43181829 | gtctcactctgtcgc[C/T]caggctggagtgcag | 23072 |
rs6943629 | snp | C/G | 0.34526 | 0.23114 | intron-variant | HECW1 | GRCh38.p7 | 7:43181776 | atattttctcatatt[C/G]ttttttgtttgtttg | 23072 |
rs6943780 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43425093 | TATTATGCAGCCTGC[C/T]GGTAATGTGGAACAG | 23072 |
rs6943852 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43395170 | catgactcctaaacc[A/G]taatttctaatcttg | 23072 |
rs6943910 | snp | C/G | 0.333722 | 0.235565 | intron-variant | HECW1 | GRCh38.p7 | 7:43181898 | gttcatgccattctc[C/G]tgcctcagcctcccg | 23072 |
rs6943915 | snp | A/G | 0.34526 | 0.23114 | intron-variant | HECW1 | GRCh38.p7 | 7:43181913 | gtgcctcagcctccc[A/G]agtagctgggactac | 23072 |
rs6944389 | snp | A/G | 0.33303 | 0.235809 | intron-variant | HECW1 | GRCh38.p7 | 7:43182229 | gaaagtatttaacca[A/G]tccaatgtcatgaaa | 23072 |
rs6944466 | snp | A/G | 0.484491 | 0.0866827 | intron-variant | HECW1 | GRCh38.p7 | 7:43382308 | aaaaaaaaaaaaaaT[A/G]GAAGCCCCTTCAGAG | 23072 |
rs6944553 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43259681 | acatctgatgtaaat[A/G]atggattgaataggc | 23072 |
rs6944604 | snp | A/G | 0.494484 | 0.0522255 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43141782 | AGATTACAGGTGTGA[A/G]CCACCGCACCCGGTG | 23072 |
rs6944786 | snp | C/T | 0.477768 | 0.103061 | intron-variant | HECW1 | GRCh38.p7 | 7:43229610 | acaaatctgcacagg[C/T]acacctgaacctaaa | 23072 |
rs6944804 | snp | C/T | 0.499713 | 0.0119774 | intron-variant | HECW1 | GRCh38.p7 | 7:43169472 | CCCTGGGAGATACAC[C/T]CTTTTCCCCATTGAG | 23072 |
rs6944922 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | HECW1 | GRCh38.p7 | 7:43412606 | tatccctcccccctc[C/G]ccccaccccaccaca | 23072 |
rs6945332 | snp | C/T | 0.172028 | 0.23753 | intron-variant | HECW1 | GRCh38.p7 | 7:43403734 | GGATGCAGTAATGAA[C/T]ATGCAGTATGTTCTC | 23072 |
rs6945335 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | HECW1 | GRCh38.p7 | 7:43169876 | TTCCCCACCCCCAGG[A/G]GACAATCCCCTACCT | 23072 |
rs6945704 | snp | A/G | 0.40386 | 0.197046 | intron-variant | HECW1 | GRCh38.p7 | 7:43166574 | GGTTAGTCACATTAC[A/G]AGTAAAAGCTTTTCT | 23072 |
rs6946828 | snp | G/T | 0.255782 | 0.249933 | intron-variant | HECW1 | GRCh38.p7 | 7:43254845 | AACTTGTCTTTGCTA[G/T]AGTCATTTATACACC | 23072 |
rs6947048 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43460764 | TGAGGCTGCAGTCCT[G/T]CCCTGAAAGACTGAG | 23072 |
rs6948701 | snp | C/T | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43416763 | ccggtctgaaaagcg[C/T]aatattcgggtggga | 23072 |
rs6949148 | snp | C/T | 0.407674 | 0.194008 | intron-variant | HECW1 | GRCh38.p7 | 7:43418907 | actctggattttgct[C/T]cagggggtattgatg | 23072 |
rs6949342 | snp | C/T | 0.476833 | 0.105105 | intron-variant | HECW1 | GRCh38.p7 | 7:43204120 | AGAACTCTTATACCT[C/T]GGCACCATAATAAAT | 23072 |
rs6950232 | snp | A/G | 0.42263 | 0.180829 | intron-variant | HECW1 | GRCh38.p7 | 7:43443721 | ACTGTGATTGTTCCT[A/G]TTCTTCATCCAGCCT | 23072 |
rs6950443 | snp | C/T | 0.436976 | 0.165952 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112825 | GCGGTCGCCAGGGTC[C/T]CCTCCCCAGCCAGTC | 23072 |
rs6952467 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | HECW1 | GRCh38.p7 | 7:43540567 | TATGGCCAGTTCTTC[C/T]TAGCAGTGACCTCGT | 23072 |
rs6952799 | snp | C/G | 0.0991586 | 0.199366 | intron-variant | HECW1 | GRCh38.p7 | 7:43314025 | agtctcactatattg[C/G]ccaggctcaaactcc | 23072 |
rs6952823 | snp | C/T | 0.0338356 | 0.126061 | intron-variant | HECW1 | GRCh38.p7 | 7:43422859 | TTAAGCTAAAAGCCC[C/T]GTCACCTGGAGATAA | 23072 |
rs6954058 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HECW1 | GRCh38.p7 | 7:43331722 | AAGGATGTTACCATG[A/G]GGTGGACGCCATCAC | 23072 |
rs6954616 | snp | A/T | 0.421209 | 0.182174 | intron-variant | HECW1 | GRCh38.p7 | 7:43417923 | acaaagtcccacaaa[A/T]tgagtggcttaaaac | 23072 |
rs6955122 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | HECW1 | GRCh38.p7 | 7:43420238 | ctaagggaagttact[A/G]tttattcctaattag | 23072 |
rs6956412 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43319735 | ctcccaaatagctga[A/G]attataggtgcctgc | 23072 |
rs6957017 | snp | C/T | 0.440333 | 0.16209 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247385 | aggcacagtggctca[C/T]gcctgtaatccagca | 23072 |
rs6957081 | snp | A/G | 0.427423 | 0.176128 | intron-variant | HECW1 | GRCh38.p7 | 7:43172094 | ACCAGCCTGGCCAAC[A/G]TGATAAGACTCTGTC | 23072 |
rs6957088 | snp | A/G | 0.40595 | 0.195396 | intron-variant | HECW1 | GRCh38.p7 | 7:43202189 | CCTAGCTAGTCAGTG[A/G]CAGAGCCAGAATTTG | 23072 |
rs6957386 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43462558 | ccaaacctactgaat[C/T]ggagactcagggggt | 23072 |
rs6957396 | snp | A/G | 0.490287 | 0.0690083 | intron-variant | HECW1 | GRCh38.p7 | 7:43462618 | CGGGTGATTCTGCGT[A/G]GCTCAGGTTGGGGAA | 23072 |
rs6957566 | snp | A/G | 0.495291 | 0.0482933 | intron-variant, nc-transcript-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161683 | TGGAGAGGTGATGAC[A/G]GTTTCCATTATTTTG | 23072 |
rs6957651 | snp | A/C | 0.159951 | 0.233219 | intron-variant | HECW1 | GRCh38.p7 | 7:43490481 | TTTTAGCATACTTTG[A/C]CAAATATCATAGGAT | 23072 |
rs6957804 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | HECW1 | GRCh38.p7 | 7:43372516 | aatgctatccctccc[C/T]gctccccACTGTTTT | 23072 |
rs6957847 | snp | A/G | 0.28578 | 0.247426 | intron-variant | HECW1 | GRCh38.p7 | 7:43344777 | taaaatttctcctct[A/G]tgttgtttaatctac | 23072 |
rs6958085 | snp | A/G | 0.302936 | 0.244331 | intron-variant | HECW1 | GRCh38.p7 | 7:43189603 | ACACATTAAAAAAAA[A/G]AAAGAGAGAAAACTT | 23072 |
rs6958416 | snp | A/G | 0.310878 | 0.242475 | intron-variant | HECW1 | GRCh38.p7 | 7:43189837 | TAAAATGTCAGTCAG[A/G]GTCACCTCACTGCCC | 23072 |
rs6958590 | snp | A/G | 0.310632 | 0.242536 | intron-variant | HECW1 | GRCh38.p7 | 7:43189914 | CATATTTTGAATCTC[A/G]GGGCTTTTTGTGTAT | 23072 |
rs6958723 | snp | A/G | 0.310386 | 0.242597 | intron-variant | HECW1 | GRCh38.p7 | 7:43190021 | ACTGAGTGTTTTCAA[A/G]GCAAATAAATGCTCT | 23072 |
rs6958724 | snp | G/T | 0.0825414 | 0.185628 | intron-variant | HECW1 | GRCh38.p7 | 7:43276139 | TTTTTCTTGTCTGTG[G/T]AAGGGATATCAGAAA | 23072 |
rs6958893 | snp | G/T | 0.224709 | 0.248717 | intron-variant | HECW1 | GRCh38.p7 | 7:43498206 | ACTCTCAGAAAATCG[G/T]GCTTAGCATTCAGAC | 23072 |
rs6958903 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | HECW1 | GRCh38.p7 | 7:43498230 | TTCAGACACCTGGAT[A/G]TGGTCCATATGGTGG | 23072 |
rs6959165 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126844 | tgtaattgctttggg[A/G]catcatgaactgcac | 23072 |
rs6959735 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127194 | ttcttggaggaaatt[A/G]aaagtgctactccaa | 23072 |
rs6959872 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127206 | attaaaagtgctact[C/G]caatgaactcctgaa | 23072 |
rs6960035 | snp | C/T | 0.348574 | 0.229746 | intron-variant | HECW1 | GRCh38.p7 | 7:43236107 | AATATACAGTAAATA[C/T]GTTTATATGCACTAG | 23072 |
rs6960577 | snp | A/G | 0.418007 | 0.185132 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120222 | TGCTCTTCCTAGAAC[A/G]TGCCAGGTACAAATA | 23072 |
rs6960763 | snp | C/T | 0.494143 | 0.0537956 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144617 | aacttgtctgggagc[C/T]cttttattgacttgt | 23072 |
rs6960889 | snp | A/G | 0.294064 | 0.246086 | intron-variant | HECW1 | GRCh38.p7 | 7:43445649 | AGTTTAAAAACAAGA[A/G]GGGCGGGGGATCGGT | 23072 |
rs6960958 | snp | C/T | 0.494143 | 0.0537956 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144776 | ttagtcctagatcag[C/T]catttctccaaggtg | 23072 |
rs6961295 | snp | A/G | 0.496175 | 0.0435625 | intron-variant | HECW1 | GRCh38.p7 | 7:43438657 | CATGGAATGACAGCA[A/G]TTAAGATGCTCACAG | 23072 |
rs6961602 | snp | A/C | 0.492918 | 0.0590819 | intron-variant | HECW1 | GRCh38.p7 | 7:43350907 | gatccattgctggtg[A/C]actagtgtgattttt | 23072 |
rs6961954 | snp | C/T | 0.199254 | 0.244796 | intron-variant | HECW1 | GRCh38.p7 | 7:43321041 | CCCTTAACTTTCACT[C/T]CATGGCTCCTCCGGG | 23072 |
rs6962062 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HECW1 | GRCh38.p7 | 7:43320950 | GCCAACCAGCCCAGA[A/G]GGCTGCCCCTTTAAT | 23072 |
rs6963606 | snp | C/T | 0.172028 | 0.23753 | intron-variant | HECW1 | GRCh38.p7 | 7:43403968 | ATGAGAAGAAATTAA[C/T]TATTCTCCTTTAACG | 23072 |
rs6963812 | snp | C/T | 0.345925 | 0.230864 | intron-variant | HECW1 | GRCh38.p7 | 7:43181888 | cacctcctgggttca[C/T]gccattctcgtgcct | 23072 |
rs6964440 | snp | C/G | 0.0923359 | 0.194016 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43127759 | aggtttaaggaaaga[C/G]actatcttcaaacat | 23072 |
rs6965038 | snp | C/T | 0.306431 | 0.243548 | intron-variant | HECW1 | GRCh38.p7 | 7:43477572 | TCCTCTACCAATTTT[C/T]CAAGGGTATATCATC | 23072 |
rs6965061 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43185917 | tctgaaaatttaaca[A/G]tcttctctcacaagg | 23072 |
rs6965080 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43516674 | TTTTCTTTGTCTTAA[A/G]TAcagtcatgtgtca | 23072 |
rs6965372 | snp | A/G | 0.305685 | 0.24372 | intron-variant | HECW1 | GRCh38.p7 | 7:43186156 | CTCTTAAACAGGAGG[A/G]TTCCATTAGAACACA | 23072 |
rs6965631 | snp | A/G | 0.046775 | 0.145601 | intron-variant | HECW1 | GRCh38.p7 | 7:43391853 | AGAGATTTGGAGGTG[A/G]AAAAGGAACTTGGGC | 23072 |
rs6965871 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HECW1 | GRCh38.p7 | 7:43179164 | CAGGTTCTTGCTTTC[C/T]GCAGAAAATAATAAA | 23072 |
rs6966529 | snp | A/G | 0.276534 | 0.248588 | intron-variant | HECW1 | GRCh38.p7 | 7:43351502 | ggggcagggctagac[A/G]tgtctgagctcagac | 23072 |
rs6966556 | snp | C/T | 0.49423 | 0.0534032 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145935 | GGTTTTTGCTCCTTC[C/T]TTCCTTGCACAGTGG | 23072 |
rs6966642 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43145818 | CTCTGTATCTTCTGT[A/G]TGTCACCTCCAGGGT | 23072 |
rs6966881 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | HECW1 | GRCh38.p7 | 7:43416900 | ctcgagcacggtgtg[C/T]gcacccactggcctg | 23072 |
rs6967190 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43440080 | CTCCGGAGGTGTCCC[A/T]CCGTGGTTAGGAGCA | 23072 |
rs6967694 | snp | A/G | 0.487305 | 0.0786545 | intron-variant | HECW1 | GRCh38.p7 | 7:43174149 | cctagccTTAAATGA[A/G]TCTTGATAGGTGGAA | 23072 |
rs6968255 | snp | C/T | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43316704 | AGAGCACCCATTCCA[C/T]ACTGAGGTGGAGAGT | 23072 |
rs6968383 | snp | C/T | 0.467744 | 0.122832 | intron-variant | HECW1 | GRCh38.p7 | 7:43221702 | GGGACTACAGGTGCC[C/T]ACCACCACGCCCGGC | 23072 |
rs6968479 | snp | A/G | 0.279726 | 0.248226 | intron-variant | HECW1 | GRCh38.p7 | 7:43221610 | CCAGGCTGGAGTGCA[A/G]TGGCGCTATCTCGGC | 23072 |
rs6968676 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124941 | ACTGTGTTTTCAAGA[C/T]GCCTTAgtttggggt | 23072 |
rs6968700 | snp | C/T | 0.329084 | 0.237162 | intron-variant | HECW1 | GRCh38.p7 | 7:43404868 | gtaatcccagctact[C/T]ggtaggttgaggcag | 23072 |
rs6968910 | snp | A/G | 0.474544 | 0.10991 | intron-variant | HECW1 | GRCh38.p7 | 7:43317192 | CTTTTCTGCAGCAGC[A/G]TCCTGTGTCTACTCT | 23072 |
rs6969180 | snp | A/G | 0.499732 | 0.0115784 | intron-variant | HECW1 | GRCh38.p7 | 7:43216295 | GGACTACAGGTGTGC[A/G]CCACCATGCCCAGCT | 23072 |
rs6969378 | snp | A/G | 0.27893 | 0.24832 | intron-variant | HECW1 | GRCh38.p7 | 7:43317264 | GCAGTGACCTACTCC[A/G]CTTGCCACTGGCTGG | 23072 |
rs6969909 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | HECW1 | GRCh38.p7 | 7:43452631 | aagattcctgccctc[A/T]tggagcttacagtct | 23072 |
rs6970166 | snp | A/G | 0.373196 | 0.217538 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151962 | TGTTCTAATTTCATG[A/G]GTAAAGACATAAATT | 23072 |
rs6970507 | snp | C/T | 0.325091 | 0.238456 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247168 | GTTTTGACTACAATG[C/T]CAAGGTGTGATCCTT | 23072 |
rs6970853 | snp | C/G | 0.318415 | 0.240457 | intron-variant | HECW1 | GRCh38.p7 | 7:43187065 | gcagtcaagacgtca[C/G]tcaaaactacaatgt | 23072 |
rs6970884 | snp | C/G | 0.206642 | 0.246211 | intron-variant | HECW1 | GRCh38.p7 | 7:43480834 | TCACCCTGCAGCCAC[C/G]TCCTCCAGATAGCAA | 23072 |
rs6971107 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | HECW1 | GRCh38.p7 | 7:43423215 | GAGCAGCCCTAAAGA[C/T]GGCATTATTTCCCCA | 23072 |
rs6971386 | snp | A/T | 0.477291 | 0.104109 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137528 | ATGCTTTCTGCCTTC[A/T]TTTATTTATTTATTT | 23072 |
rs6972018 | snp | G/T | 0.162581 | 0.234218 | intron-variant | HECW1 | GRCh38.p7 | 7:43401484 | GATAATTTTGAGTAT[G/T]TAAATTAAAGAAGAC | 23072 |
rs6972237 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | HECW1 | GRCh38.p7 | 7:43535704 | TGTCCGTACTGTACC[A/G]TGGTGGGAACATGAT | 23072 |
rs6972287 | snp | G/T | 0.394538 | 0.203982 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160952 | TTTCCTTATTTAAAT[G/T]TTATAACATCTCTCC | 23072 |
rs6972702 | snp | A/C | 0.471483 | 0.115954 | intron-variant | HECW1 | GRCh38.p7 | 7:43388149 | GCCTGGCTGCCTCTT[A/C]ACACCATATTGTACA | 23072 |
rs6972794 | snp | A/T | 0.498754 | 0.0249289 | intron-variant | HECW1 | GRCh38.p7 | 7:43226252 | ATAAAAGTTCAAATG[A/T]TACAAACTCTAGCCT | 23072 |
rs6972797 | snp | A/G | 0.292008 | 0.246445 | intron-variant | HECW1 | GRCh38.p7 | 7:43252373 | AGCTGTCTTAGGGCC[A/G]TGTGTACTTACACCC | 23072 |
rs6973014 | snp | A/G | 0.441841 | 0.160303 | intron-variant | HECW1 | GRCh38.p7 | 7:43205272 | gtatttttagtagag[A/G]tggtgtttcactatg | 23072 |
rs6973216 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43476134 | CAATTAAAAATCCAA[A/G]AGGATATACTTAAGA | 23072 |
rs6973286 | snp | A/C | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43317549 | GATTTTGGATTTCTG[A/C]AGCTGACCCTGTCAA | 23072 |
rs6973466 | snp | A/C | 0.266273 | 0.24947 | intron-variant | HECW1 | GRCh38.p7 | 7:43252724 | TCTATAGGTAAATAT[A/C]ACTAGCAGTTGGCCA | 23072 |
rs6974565 | snp | A/G | 0.497329 | 0.0364438 | intron-variant | HECW1 | GRCh38.p7 | 7:43459115 | CCTGAAACATATCTC[A/G]TCCTACAGACCTGAC | 23072 |
rs6974808 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HECW1 | GRCh38.p7 | 7:43459024 | Agccattccccagac[A/G]cggcacactcttcca | 23072 |
rs6974993 | snp | A/G | 0.425432 | 0.178112 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247637 | agcaagaTGCTATgg[A/G]aggaaagaaagagag | 23072 |
rs6975053 | snp | A/G | 0.425277 | 0.178263 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247419 | tgggagggggatagc[A/G]ggaggatagcttgag | 23072 |
rs6975079 | snp | A/G | 0.476487 | 0.105846 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43247462 | aagcctgggcaacat[A/G]gtgagaccccatctc | 23072 |
rs6975189 | snp | C/T | 0.29046 | 0.246704 | intron-variant | HECW1 | GRCh38.p7 | 7:43369146 | AGGAAATATAAATGT[C/T]ACTCTTTGCTGACAT | 23072 |
rs6975459 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | HECW1 | GRCh38.p7 | 7:43453479 | aggatccaacacttg[C/G]tttcgatcatcctgt | 23072 |
rs6975628 | snp | C/T | 0.0252325 | 0.109451 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43296582 | CTCTCTCAACCCTGG[C/T]GCTCTGATGTCCAAG | 23072 |
rs6975708 | snp | A/T | 0.268452 | 0.249318 | intron-variant | HECW1 | GRCh38.p7 | 7:43319470 | GAGGTGAAAGCACAC[A/T]GTCACCCAGAGCTCC | 23072 |
rs6975782 | snp | G/T | 0.46974 | 0.119223 | intron-variant | HECW1 | GRCh38.p7 | 7:43210560 | gcaagcctcgtgttc[G/T]ctaacctggggttct | 23072 |
rs6976013 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43319627 | ttttttttttttttg[G/T]gagacagagtctcgc | 23072 |
rs6976250 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | HECW1 | GRCh38.p7 | 7:43240934 | CTGCTGCCCTGTGCC[A/G]AGCACTCCTAGAGGA | 23072 |
rs6976453 | snp | A/G | 0.465368 | 0.126951 | intron-variant | HECW1 | GRCh38.p7 | 7:43394135 | GTGGAGGTCTCCCAC[A/G]GCCATGTCCAGGCAC | 23072 |
rs6976862 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43394123 | GGTGGTCAGCATGTG[A/G]AGGTCTCCCACAGCC | 23072 |
rs6977016 | snp | A/G | 0.494358 | 0.0528145 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147874 | ACTTAGCATTGTTTT[A/G]CTAAACTTTATATCC | 23072 |
rs6977024 | snp | A/G | 0.494358 | 0.0528145 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147879 | GCATTGTTTTACTAA[A/G]CTTTATATCCCTAAG | 23072 |
rs6977089 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43314364 | CAGACACCTTGGGGG[G/T]GGATAAGCTCACTCT | 23072 |
rs6977397 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147799 | ACAGTAGTCTTGCCA[A/G]AATGATGTTTGGGTT | 23072 |
rs6977617 | snp | A/G | 0.142272 | 0.225598 | intron-variant | HECW1 | GRCh38.p7 | 7:43323627 | aaacacaacaacaac[A/G]acaaaaaTACATTAT | 23072 |
rs6977971 | snp | C/T | 0.482609 | 0.0916147 | intron-variant | HECW1 | GRCh38.p7 | 7:43381751 | ctggtcgcaaactct[C/T]gacctcaggtgatct | 23072 |
rs6978271 | snp | A/G | 0.248471 | 0.249995 | intron-variant | HECW1 | GRCh38.p7 | 7:43228947 | AAATTGGTTAACAGT[A/G]GTAGATTCTGCATCA | 23072 |
rs6978738 | snp | A/G | 0.192088 | 0.2432 | intron-variant | HECW1 | GRCh38.p7 | 7:43477105 | TGTTTTTCTTTTGTA[A/G]ATTCCCTGGGAAATT | 23072 |
rs6978743 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126462 | TTAAAGCTACTGCCA[C/T]GCTATAATGGCAGAG | 23072 |
rs6979521 | snp | A/C | 0.125528 | 0.21681 | intron-variant | HECW1 | GRCh38.p7 | 7:43369505 | TTTGACAGTCTTGGT[A/C]CTGTTAAAAGTCTAC | 23072 |
rs6979980 | snp | A/G | 0.307176 | 0.243374 | intron-variant | HECW1 | GRCh38.p7 | 7:43194132 | caaagggaggagggt[A/G]tcatgaggcgtgtcc | 23072 |
rs6980106 | snp | C/T | 0.179105 | 0.239737 | intron-variant | HECW1 | GRCh38.p7 | 7:43407162 | GACTGCACTCAGCCC[C/T]GTGGAGGCCAGGTCT | 23072 |
rs6980464 | snp | G/T | 0.25634 | 0.24992 | intron-variant | HECW1 | GRCh38.p7 | 7:43366369 | CTTCCCCAAATTCTA[G/T]GTCATTACCTTTGGC | 23072 |
rs7341456 | snp | C/T | 0.415727 | 0.187175 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147056 | GCCAGCAGTGGGTAA[C/T]GGAAATTTTGTACTT | 23072 |
rs7350018 | snp | A/G | 0.22263 | 0.248497 | intron-variant | HECW1 | GRCh38.p7 | 7:43409204 | GGACGTGAGGGAAAT[A/G]GACTTGTACTTAAAC | 23072 |
rs7357306 | snp | G/T | 0.491987 | 0.0627894 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155665 | ACCTCTCTACTCAGT[G/T]TGTATTACCGTTTTG | 23072 |
rs7357307 | snp | A/T | 0.486266 | 0.0817214 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43155666 | CCTCTCTACTCAGTT[A/T]GTATTACCGTTTTGA | 23072 |
rs7384889 | snp | C/T | 0.45762 | 0.139261 | intron-variant | HECW1 | GRCh38.p7 | 7:43415541 | agagtatctttgtgg[C/T]gttctctgtatttcc | 23072 |
rs7455224 | snp | A/G | 0.289942 | 0.246789 | intron-variant | HECW1 | GRCh38.p7 | 7:43395203 | gctaacgttagtcct[A/G]caaagacaatctagt | 23072 |
rs7455724 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43242560 | ATGGTGCTTGGGTGG[C/G]TGCGCAAAGCTCCAG | 23072 |
rs7456624 | snp | C/G | 0.458084 | 0.138567 | intron-variant | HECW1 | GRCh38.p7 | 7:43414937 | ttggttgtgtctctg[C/G]ccggctttggtatca | 23072 |
rs7456690 | snp | A/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43533279 | AACTTAACCCATGCA[A/T]GTCCTGGTCCATTAC | 23072 |
rs7457207 | snp | A/G | 0.416218 | 0.186739 | intron-variant | HECW1 | GRCh38.p7 | 7:43415537 | tcgaagagtatcttt[A/G]tggcgttctctgtat | 23072 |
rs7777192 | snp | A/C | 0.498437 | 0.0279115 | intron-variant | HECW1 | GRCh38.p7 | 7:43454839 | AGCTATGGCTTTTCT[A/C]ACTGAAAAGGCTGGA | 23072 |
rs7778581 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | HECW1 | GRCh38.p7 | 7:43507561 | ACAAGAAATCTTGAA[C/T]TAAATAAAAAATCTC | 23072 |
rs7778630 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43315485 | TATTATTATTATTAT[C/T]ATTATTATCATTATT | 23072 |
rs7778631 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315493 | TTATTATTATTATTA[C/T]CATTATTACTATTAT | 23072 |
rs7778944 | snp | G/T | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43315730 | aactcctgacctcag[G/T]tgatccacccacctc | 23072 |
rs7779089 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | HECW1 | GRCh38.p7 | 7:43470642 | CCCCTAATTCTCTTT[A/G]GCAAGAAGATATCAT | 23072 |
rs7779274 | snp | A/G | 0.357238 | 0.225832 | intron-variant | HECW1 | GRCh38.p7 | 7:43382894 | ggttttaagccccac[A/G]tgcattaggggtttg | 23072 |
rs7779437 | snp | A/C | 0.492775 | 0.059668 | intron-variant | HECW1 | GRCh38.p7 | 7:43467360 | TCCAGGCAGAGGGAC[A/C]TCTGTAGAAAGGATG | 23072 |
rs7779443 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43200009 | gaagtcactaagcgt[C/T]gctcaatttttataa | 23072 |
rs7779785 | snp | A/G | 0.492679 | 0.0600586 | intron-variant | HECW1 | GRCh38.p7 | 7:43467303 | CATTCTTGGGGAGGC[A/G]GCTGAATTGAGTCCT | 23072 |
rs7780105 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | HECW1 | GRCh38.p7 | 7:43467502 | TGCAAAGGAGCCTGG[A/G]TCTACTGCAGCAGGC | 23072 |
rs7781109 | snp | A/T | 0.478354 | 0.101757 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130205 | TTTTGACATTGTATA[A/T]GTGTATATTAcaggt | 23072 |
rs7781407 | snp | A/G | 0.235273 | 0.249566 | intron-variant | HECW1 | GRCh38.p7 | 7:43461128 | ACATTTCTTCTTACC[A/G]TTATTTCTCATGGTT | 23072 |
rs7781550 | snp | C/T | 0.428182 | 0.17536 | intron-variant | HECW1 | GRCh38.p7 | 7:43179047 | GAAGTGCCAGGCCCT[C/T]CACAAGTAACACCGA | 23072 |
rs7781890 | snp | A/G | 0.21695 | 0.247806 | intron-variant | HECW1 | GRCh38.p7 | 7:43367634 | ATGATTTATTTACAT[A/G]CAAAGGATCAATGCT | 23072 |
rs7782118 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138568 | CTGGATATGTACTTG[C/T]CTGCACAGTCTATTT | 23072 |
rs7782196 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | HECW1 | GRCh38.p7 | 7:43270576 | gacaagctctggttc[A/G]gtgtggaagggcact | 23072 |
rs7782660 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HECW1 | GRCh38.p7 | 7:43448982 | TCAGTCGGCTGAGAC[A/G]TGTTGGTCACATCAT | 23072 |
rs7782684 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, nc-transcript-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43300884 | TGCACACTGTCCCTG[C/T]ACCCGCCCAGGAGCC | 23072 |
rs7782895 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43426239 | CTTTCAAATATTTGC[A/G]TCCCTTCTAGTACTG | 23072 |
rs7782954 | snp | A/G | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43182902 | atctttcacttcctt[A/G]gttaaatttttccta | 23072 |
rs7783044 | snp | A/C | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43183202 | CTCACTACTTAGGTT[A/C]TAACTGAGTTACAGT | 23072 |
rs7783118 | snp | A/T | 0.493837 | 0.055168 | intron-variant | HECW1 | GRCh38.p7 | 7:43355474 | tagaggctttttttt[A/T]aatttgttctttgtt | 23072 |
rs7783147 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43183206 | CTACTTAGGTTATAA[C/T]TGAGTTACAGTAACA | 23072 |
rs7783180 | snp | A/G | 0.38555 | 0.210062 | intron-variant | HECW1 | GRCh38.p7 | 7:43449061 | CAGGCAGTCAACAAT[A/G]TTGTATTTCCACTAG | 23072 |
rs7783707 | snp | C/T | 0.305934 | 0.243663 | intron-variant | HECW1 | GRCh38.p7 | 7:43177603 | CTAGCCCTGGCTCTG[C/T]TACTTGTCACCTGTG | 23072 |
rs7784001 | snp | C/T | 0.364609 | 0.222182 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268093 | ACAACTTATAATTTA[C/T]GCATTTATTTTAAAA | 23072 |
rs7784053 | snp | A/G | 0.353371 | 0.227628 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268218 | AAACAGACATTTCCA[A/G]CTCAGCTACAGAATT | 23072 |
rs7784124 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HECW1 | GRCh38.p7 | 7:43318553 | GCAGATTACAAGTAG[A/G]CTTACCAGTTATCTC | 23072 |
rs7784203 | snp | A/G | 0.46014 | 0.13543 | intron-variant | HECW1 | GRCh38.p7 | 7:43348939 | cctatcatatgatct[A/G]tcttggagaaagttc | 23072 |
rs7785443 | snp | A/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43186519 | aaaaatacaaaaaaa[A/T]ttacccaggcttggt | 23072 |
rs7785605 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43186647 | gcactccagcctggg[C/T]gacagagcgagactc | 23072 |
rs7785614 | snp | C/G | 0.492823 | 0.0594727 | intron-variant | HECW1 | GRCh38.p7 | 7:43283604 | ataaaagttctttag[C/G]atcctcaataatatt | 23072 |
rs7785628 | snp | A/G | 0.243919 | 0.249926 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130668 | atcaccagaatacct[A/G]tatcagctgttagac | 23072 |
rs7785719 | snp | C/T | 0.472147 | 0.114677 | intron-variant | HECW1 | GRCh38.p7 | 7:43304642 | GATTACAGACACGTG[C/T]CACCACACATGGCTA | 23072 |
rs7785861 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131046 | caaggcgggtgaatc[A/G]ctggaggtcaggagt | 23072 |
rs7786005 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43489705 | AAGACTACCACACAC[A/G]GAGAGTGAACTGGTG | 23072 |
rs7786169 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HECW1 | GRCh38.p7 | 7:43496785 | TGCGGTGAAAAGCAG[A/G]AAGCCACATGTAGAG | 23072 |
rs7786298 | snp | C/T | 0.439085 | 0.163545 | intron-variant | HECW1 | GRCh38.p7 | 7:43179827 | GGGAGAGTTCATTTT[C/T]GAAAACATGATTGAG | 23072 |
rs7786509 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HECW1 | GRCh38.p7 | 7:43284026 | agagatgtggggaTT[A/G]AGTCAGGGGCCTGGG | 23072 |
rs7786564 | snp | G/T | 0.331411 | 0.236373 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43131282 | aaaaaaaTTTTTTTT[G/T]Tatttaatccttcca | 23072 |
rs7786567 | snp | A/G | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43189249 | ATAGGCCATATCATA[A/G]CTACTCAAATTTTAA | 23072 |
rs7786662 | snp | A/G | 0.389715 | 0.207315 | intron-variant | HECW1 | GRCh38.p7 | 7:43497154 | GGGAAGGCTTTTCCA[A/G]GTAGGTGATGCTTAA | 23072 |
rs7787143 | snp | A/C | 0.233527 | 0.249457 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43118620 | TTTTTCTTTACCGTT[A/C]TTCATAATTCCTTGT | 23072 |
rs7787227 | snp | A/G | 0.442655 | 0.159323 | intron-variant | HECW1 | GRCh38.p7 | 7:43183396 | ATGCAAACATCCTCC[A/G]CCCTCAATACACAAT | 23072 |
rs7787356 | snp | A/G | 0.494143 | 0.0537956 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43148587 | taggtaaacagTGTT[A/G]GATACTTAAATTTGG | 23072 |
rs7787852 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43184037 | ttttttttttgagac[A/G]aagtctcgctctgtt | 23072 |
rs7787964 | snp | C/T | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43184036 | tttttttttttgaga[C/T]aaagtctcgctctgt | 23072 |
rs7788485 | snp | C/T | 0.132751 | 0.2208 | intron-variant | HECW1 | GRCh38.p7 | 7:43231351 | GGTGTTTTCACATGA[C/T]GTGGATTCACTGAAT | 23072 |
rs7788720 | snp | A/G | 0.175254 | 0.238565 | intron-variant | HECW1 | GRCh38.p7 | 7:43356491 | ccactctccataatg[A/G]ccatatcattccagc | 23072 |
rs7788725 | snp | C/T | 0.482534 | 0.0918038 | intron-variant | HECW1 | GRCh38.p7 | 7:43349472 | gaagttcccccacta[C/T]tattatgttgctgtc | 23072 |
rs7788904 | snp | A/G | 0.491104 | 0.0660973 | intron-variant | HECW1 | GRCh38.p7 | 7:43356634 | ttcagaatagaccat[A/G]tattaagccacaaaa | 23072 |
rs7789382 | snp | A/G | 0.329084 | 0.237162 | intron-variant | HECW1 | GRCh38.p7 | 7:43262162 | GGAGATGGAGGTTGC[A/G]GTGAGCTGAGATTGC | 23072 |
rs7790085 | snp | C/G | 0.32768 | 0.237625 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161468 | TGGTGCACAGCACAG[C/G]CCTAGGCAGTATCTG | 23072 |
rs7790444 | snp | A/G | 0.46845 | 0.121572 | intron-variant | HECW1 | GRCh38.p7 | 7:43402387 | tccctctcccataag[A/G]ggtttgagcatacga | 23072 |
rs7790685 | snp | A/G | 0.496382 | 0.0423778 | intron-variant | HECW1 | GRCh38.p7 | 7:43557799 | TGTACTCATTTGCAC[A/G]TATGTGTGTGTATAT | 23072 |
rs7790693 | snp | C/T | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43180289 | TCTAGCTCCCACTCC[C/T]TTTAATGGTTGGAGG | 23072 |
rs7790786 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43189365 | AATTAGCTCTCAGGC[A/G]ATAGGGACATTGCTG | 23072 |
rs7792143 | snp | A/T | 0.417683 | 0.185425 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43515453 | GATATTAAAGAATCA[A/T]AATAGGGCAGAAGCA | 23072 |
rs7792151 | snp | C/G | 0.494936 | 0.050064 | intron-variant | HECW1 | GRCh38.p7 | 7:43244454 | GACTTCCTGCCAATG[C/G]TCCTCCTTCCTCTGT | 23072 |
rs7792705 | snp | C/T | 0.398354 | 0.201224 | intron-variant | HECW1 | GRCh38.p7 | 7:43499341 | GAGTGTGGCGGTGCA[C/T]GCCTATAATCCCAGC | 23072 |
rs7792824 | snp | C/T | 0.482459 | 0.0919928 | intron-variant | HECW1 | GRCh38.p7 | 7:43469339 | TCCTAGCCCTCACGC[C/T]GCTAGATGCCAACTG | 23072 |
rs7793354 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | HECW1 | GRCh38.p7 | 7:43507007 | cccaggaggtggaag[C/T]tgcggtaagccgaga | 23072 |
rs7794076 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | HECW1 | GRCh38.p7 | 7:43378310 | GTGTACACAGTGACT[A/G]CTGGATGAGGAGAGA | 23072 |
rs7794108 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114840 | TGGAACAGCCCATCA[A/G]TGTATCAATACAGAG | 23072 |
rs7794329 | snp | G/T | 0.167809 | 0.236103 | intron-variant, utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563587 | ACTCTAAAGCATTCC[G/T]gccaggagcggtggc | 23072 |
rs7794383 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | HECW1 | GRCh38.p7 | 7:43290590 | tccatttttcaggtt[C/T]ctctggggtcatcct | 23072 |
rs7794449 | snp | C/G | 0.484279 | 0.0872533 | intron-variant | HECW1 | GRCh38.p7 | 7:43378337 | GAGAGGAGAGGACTT[C/G]TCAGGAATAGGATTA | 23072 |
rs7794462 | snp | A/G | 0.438386 | 0.164349 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43114820 | AGGGAGGTCACATCC[A/G]GAGCTGGAACAGCCC | 23072 |
rs7794492 | snp | A/G | 0.26078 | 0.249767 | intron-variant | HECW1 | GRCh38.p7 | 7:43415984 | tttgaatgtcctccc[A/G]tagctcagagtaatt | 23072 |
rs7794675 | snp | A/G | 0.29175 | 0.246489 | intron-variant | HECW1 | GRCh38.p7 | 7:43415822 | ccagttgatcgcatc[A/G]gctcctgaggcttct | 23072 |
rs7794848 | snp | A/G | 0.321053 | 0.23969 | intron-variant | HECW1 | GRCh38.p7 | 7:43473975 | ACATGATAAACTTAG[A/G]TACCAAAAGGAAAAC | 23072 |
rs7795330 | snp | A/C | 0.160938 | 0.233598 | intron-variant | HECW1 | GRCh38.p7 | 7:43345576 | gtcttttatccctcg[A/C]tcccctctcactctt | 23072 |
rs7795391 | snp | G/T | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43312251 | TGTTTTTCTGCAAAA[G/T]GGACAATAAGGTCTC | 23072 |
rs7795449 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | HECW1 | GRCh38.p7 | 7:43474245 | ACGAGGTCAGCAGAT[C/G]GAGACCACCCTAGCT | 23072 |
rs7795543 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43315494 | TATTATTATTATTAT[C/T]ATTATTACTATTATT | 23072 |
rs7795607 | snp | C/G | 0.499968 | 0.00399348 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43162752 | CAGAGGTAGTGGTCC[C/G]TATAAACAAAGCTCC | 23072 |
rs7796172 | snp | C/T | 0.498415 | 0.0281103 | intron-variant | HECW1 | GRCh38.p7 | 7:43454838 | AAGCTATGGCTTTTC[C/T]CACTGAAAAGGCTGG | 23072 |
rs7796495 | snp | A/G | 0.499551 | 0.0149693 | intron-variant | HECW1 | GRCh38.p7 | 7:43228158 | TAAAAAGCAAATAAC[A/G]CCCAGGGAAAATATT | 23072 |
rs7797012 | snp | A/G | 0.493013 | 0.058691 | intron-variant | HECW1 | GRCh38.p7 | 7:43185400 | actcgaggggtaaat[A/G]gtcggaactgtctca | 23072 |
rs7797487 | snp | A/G | 0.410905 | 0.191336 | intron-variant | HECW1 | GRCh38.p7 | 7:43333518 | ATCAAAGCAAAAATC[A/G]TCTATAATTTCAACA | 23072 |
rs7797616 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43208424 | TAAGTGTTCTCTTCA[A/G]CTGTTTTATTATCCT | 23072 |
rs7797811 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | HECW1 | GRCh38.p7 | 7:43421696 | aacttattttgacat[C/G]caggaatgaaaatta | 23072 |
rs7798517 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115443 | GATAATTGAGAATTC[A/G]CTTTTTCCAATCATT | 23072 |
rs7798947 | snp | A/G | 0.276534 | 0.248588 | intron-variant | HECW1 | GRCh38.p7 | 7:43263704 | AGGAGAAATACTAGG[A/G]AACagagaagaaggg | 23072 |
rs7799671 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | HECW1 | GRCh38.p7 | 7:43370470 | aactaaacataccct[C/T]accatatgattcagc | 23072 |
rs7800505 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | HECW1 | GRCh38.p7 | 7:43380144 | tgcaactttgacctc[C/T]tgtgctcaagcaatc | 23072 |
rs7800809 | snp | C/T | 0.308414 | 0.24308 | intron-variant | HECW1 | GRCh38.p7 | 7:43330334 | CTGGCAGGCCCAGAG[C/T]TTCCAGCCATCCTCA | 23072 |
rs7800963 | snp | A/T | 0.499 | 0.0223418 | intron-variant | HECW1 | GRCh38.p7 | 7:43330414 | CAACAGCATGTGAGA[A/T]CCGCAGGAGAACTGC | 23072 |
rs7801372 | snp | C/T | 0.249886 | 0.25 | intron-variant | HECW1 | GRCh38.p7 | 7:43388441 | CCATTGATTTTCATA[C/T]TGCCAAGCTAGAAAA | 23072 |
rs7801731 | snp | A/C | 0.371582 | 0.218444 | intron-variant | HECW1 | GRCh38.p7 | 7:43375051 | AATAAAGTTTTAAAA[A/C]TAAAATGTTCTTTTG | 23072 |
rs7802054 | snp | A/C | 0.426507 | 0.177046 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517323 | TTTGCTAACTGCAAA[A/C]TAAACAGACTCCCCT | 23072 |
rs7802134 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43375254 | TTTGAATGTTCTCTT[C/T]ACAGCACAAAGATGT | 23072 |
rs7802327 | snp | A/G | 0.423413 | 0.180077 | intron-variant | HECW1 | GRCh38.p7 | 7:43179324 | GGAGACTGTAATATT[A/G]ATAGAAGCCCCTTAC | 23072 |
rs7802336 | snp | A/C | 0.426966 | 0.176587 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517511 | ATTAAGTGTAATTGT[A/C]GAGTTTTATGGAACT | 23072 |
rs7802446 | snp | C/T | 0.453697 | 0.14494 | intron-variant | HECW1 | GRCh38.p7 | 7:43179334 | ATATTAATAGAAGCC[C/T]CTTACTCCCAAGTCT | 23072 |
rs7802542 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43355596 | atgcaaaacctataa[C/T]agattcactaaaaat | 23072 |
rs7803038 | snp | G/T | 0.496874 | 0.0394129 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43268168 | CCTGTGTGTGCAGAG[G/T]CTCTGCCCTCAGGGT | 23072 |
rs7803525 | snp | C/T | 0.472335 | 0.114312 | intron-variant | HECW1 | GRCh38.p7 | 7:43305283 | TAAGATGAAACATTT[C/T]GTTAAGAACTTGGAG | 23072 |
rs7803610 | snp | A/C | 0.493107 | 0.0583 | intron-variant | HECW1 | GRCh38.p7 | 7:43180106 | GAGTTGGTAACATTC[A/C]CTTTTATGCAAGATG | 23072 |
rs7804641 | snp | G/T | 0.195837 | 0.244062 | intron-variant | HECW1 | GRCh38.p7 | 7:43168150 | TGGACATGTTTCACT[G/T]TTGCATGATGTCCCC | 23072 |
rs7805119 | snp | G/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43188884 | GTTAGAAACAATTCA[G/T]GAAAAGTCATCGGGG | 23072 |
rs7806590 | snp | C/G | 0.475081 | 0.108804 | intron-variant | HECW1 | GRCh38.p7 | 7:43318162 | TATAAATCCCTGACC[C/G]TGACTATTAAAGGGA | 23072 |
rs7806923 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43184065 | gttgcccaggctgga[G/T]tgcagtggctagatc | 23072 |
rs7807450 | snp | A/G | 0.438946 | 0.163706 | intron-variant | HECW1 | GRCh38.p7 | 7:43305363 | ATCTTCTTGGCTGCC[A/G]AGAAGCTCAGAGAAG | 23072 |
rs7807551 | snp | C/T | 0.391954 | 0.205789 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152778 | CATTCCGGGGGCCCT[C/T]GGGTCTTCATATCTG | 23072 |
rs7807665 | snp | C/T | 0.491157 | 0.065903 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152803 | TATCTGTAGGCGTTT[C/T]CCCCTGAGCTGGTTG | 23072 |
rs7807881 | snp | A/G | 0.368938 | 0.219895 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43153049 | GCCAGCTTTCCCTAT[A/G]TACACCTTCTCTTAT | 23072 |
rs7808143 | snp | A/G | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43180873 | tcctctcttgtaact[A/G]ttttgaaatatgcaa | 23072 |
rs7808221 | snp | A/G | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43180671 | aagtgctgggattac[A/G]ggcgtgagccaccgc | 23072 |
rs7808261 | snp | A/C | 0.306431 | 0.243548 | intron-variant | HECW1 | GRCh38.p7 | 7:43180843 | ataatttctttgtag[A/C]aagaatatttagaat | 23072 |
rs7808277 | snp | A/C | 0.19334 | 0.243495 | intron-variant | HECW1 | GRCh38.p7 | 7:43424045 | CAGGTGGGAGAGAAC[A/C]AAAGAAATTTCAGAG | 23072 |
rs7808508 | snp | C/T | 0.327211 | 0.237778 | intron-variant | HECW1 | GRCh38.p7 | 7:43262112 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 23072 |
rs7808663 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43481948 | ccactgcactccagc[C/T]tgagcgacacagcga | 23072 |
rs7808837 | snp | A/C | 0.490175 | 0.0693959 | intron-variant | HECW1 | GRCh38.p7 | 7:43353458 | tagtatagaggcaag[A/C]tggcttcacttcccc | 23072 |
rs7808981 | snp | A/C | 0.364609 | 0.222182 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269204 | GCCTGCCATTCATAC[A/C]CCTTGCCATCTCCTA | 23072 |
rs7808993 | snp | G/T | 0.34526 | 0.23114 | intron-variant | HECW1 | GRCh38.p7 | 7:43181170 | catgttgtggcaaat[G/T]acaccatttcattct | 23072 |
rs7809096 | snp | C/T | 0.499563 | 0.0147699 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269191 | ACTTCTTCAGTTTGC[C/T]TGCCATTCATACACC | 23072 |
rs7809124 | snp | C/G | 0.34526 | 0.23114 | intron-variant | HECW1 | GRCh38.p7 | 7:43181242 | actttatccattcat[C/G]tcttgatggatactt | 23072 |
rs7809466 | snp | A/G | 0.41441 | 0.188333 | intron-variant | HECW1 | GRCh38.p7 | 7:43469288 | CTCAGCACTACTCTG[A/G]GGAATACCCTGTGCC | 23072 |
rs7810023 | snp | A/T | 0.208169 | 0.246476 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520658 | CTTTAAGGTTTTTTT[A/T]AAAAAAAACACAAAG | 23072 |
rs7810040 | snp | A/T | 0.0763149 | 0.179815 | intron-variant | HECW1 | GRCh38.p7 | 7:43506991 | agcagaatcgcttga[A/T]cccaggaggtggaag | 23072 |
rs7810051 | snp | A/G | 0.309894 | 0.242719 | intron-variant | HECW1 | GRCh38.p7 | 7:43507005 | AACCCAGGAGGTGGA[A/G]GTTGCGGTAAGCCGA | 23072 |
rs7810100 | snp | C/T | 0.177182 | 0.23916 | intron-variant | HECW1 | GRCh38.p7 | 7:43176015 | ATTCTTCTCAGTGAG[C/T]CATGTAGTGTTTTCT | 23072 |
rs7810171 | snp | C/T | 0.440195 | 0.162252 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520763 | GGAGGGGTGCCTGGT[C/T]CACTGAGCCCCTCAG | 23072 |
rs7810582 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HECW1 | GRCh38.p7 | 7:43199036 | TATGACCACAAATCC[A/G]ATATAAGAGAGTCCA | 23072 |
rs7810627 | snp | C/T | 0.233527 | 0.249457 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43135496 | CCTCCCACCCCAGAT[C/T]TGTCCATCTCTGGAC | 23072 |
rs7810701 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | HECW1 | GRCh38.p7 | 7:43190181 | tgcagtggcatgatc[G/T]cggcccactgcaacc | 23072 |
rs7810766 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HECW1 | GRCh38.p7 | 7:43244389 | CTCATTAGGATGGGC[C/T]CTTGCAGCAGGGTTG | 23072 |
rs7811003 | snp | A/G | 0.484701 | 0.0861117 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376530 | CCTAAATGGCCTCTC[A/G]ATAAAAACTCTTTGT | 23072 |
rs7811136 | snp | A/G | 0.428635 | 0.174898 | intron-variant | HECW1 | GRCh38.p7 | 7:43554488 | CAGATCAAAAGCAGC[A/G]GTTCCGTTCCTATCA | 23072 |
rs7811238 | snp | C/T | 0.0577344 | 0.159793 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376587 | ATTTCAAATATAGCT[C/T]ggcacagtggcttac | 23072 |
rs9638972 | snp | C/T | 0.233235 | 0.249437 | intron-variant | HECW1 | GRCh38.p7 | 7:43554872 | TTTTGAGTGACCATC[C/T]TTTGGGATGGAATTC | 23072 |
rs9639869 | snp | A/T | 0.4944 | 0.0526182 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43142483 | GGGTCGAGGGTGGGC[A/T]GCTGTGCCCACCAGT | 23072 |
rs9639872 | snp | C/T | 0.492484 | 0.0608394 | intron-variant | HECW1 | GRCh38.p7 | 7:43260017 | cacccaggcacatca[C/T]agtcaaacttctgaa | 23072 |
rs9639873 | snp | C/T | 0.498415 | 0.0281103 | intron-variant | HECW1 | GRCh38.p7 | 7:43374405 | GTGACTTAGAGACCA[C/T]GGGAAAAGGAATTAC | 23072 |
rs9639874 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | HECW1 | GRCh38.p7 | 7:43375407 | ACATGTCAAATATAC[A/G]ATTTCAGGATTGCGA | 23072 |
rs9639876 | snp | A/G | 0.118584 | 0.212673 | intron-variant | HECW1 | GRCh38.p7 | 7:43472584 | taattaagtattaat[A/G]ttaattatattaaat | 23072 |
rs9639877 | snp | C/T | 0.299664 | 0.245017 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509258 | GAGTGAATGACAGAG[C/T]CCAAGAAGGAAGAAT | 23072 |
rs9639879 | snp | C/T | 0.273856 | 0.248859 | intron-variant | HECW1 | GRCh38.p7 | 7:43547494 | agagattgcagcaag[C/T]caggattgcgccact | 23072 |
rs9639880 | snp | A/G | 0.233235 | 0.249437 | intron-variant | HECW1 | GRCh38.p7 | 7:43553881 | CTTTGCACGCTGCTC[A/G]TAGCTTCACTTCCTT | 23072 |
rs9648078 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | HECW1 | GRCh38.p7 | 7:43280814 | CCCAGCCAACTATAT[A/C]CTCAGGTGGACAATA | 23072 |
rs9648079 | snp | A/G | 0.496517 | 0.0415876 | intron-variant | HECW1 | GRCh38.p7 | 7:43280832 | CAGGTGGACAATAAC[A/G]CTCTTGCTCACTAGG | 23072 |
rs9648531 | snp | C/T | 0.437118 | 0.165792 | intron-variant | HECW1 | GRCh38.p7 | 7:43552903 | CTTTCCTTCAGGTGA[C/T]ATCGTCCTCATATTG | 23072 |
rs9648532 | snp | C/T | 0.437118 | 0.165792 | intron-variant | HECW1 | GRCh38.p7 | 7:43552982 | ATCCAGGACCCAGCT[C/T]CTGAGCAGTGTGCAT | 23072 |
rs9648533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43553112 | GCTAATGTCTAACCC[C/T]TCCTAAATACTCACC | 23072 |
rs9655043 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | HECW1 | GRCh38.p7 | 7:43175243 | AACATTCATTCCCTC[A/G]CACACTTACCATTTT | 23072 |
rs9655440 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138854 | CAGATAAAGAGGCCt[A/G]aacaaagagaaacag | 23072 |
rs9655441 | snp | G/T | 0.0558544 | 0.157504 | intron-variant | HECW1 | GRCh38.p7 | 7:43367364 | ATGATGAGACAAAAT[G/T]TTGAGACTTAGTCCC | 23072 |
rs9655442 | snp | A/G | 0.300169 | 0.244914 | intron-variant | HECW1 | GRCh38.p7 | 7:43436302 | AGACTTCCTCTTCCC[A/G]GGTAGTTTGGGCTGG | 23072 |
rs9719061 | snp | A/G | | | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43302957 | cacacacatgcgcgc[A/G]cacacacacacaGGA | 23072 |
rs9770050 | snp | A/T | 0.350982 | 0.228698 | intron-variant | HECW1 | GRCh38.p7 | 7:43184023 | attattattattatt[A/T]ttttttttgagacaa | 23072 |
rs9770992 | snp | A/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43184008 | tttgccaattctttt[A/T]ttattattattattt | 23072 |
rs9791927 | snp | A/G | 0.111576 | 0.20818 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43124290 | TGTTGGTATAAATTC[A/G]CAAATAGCTTTTGAG | 23072 |
rs10215158 | snp | C/G | 0.306431 | 0.243548 | intron-variant | HECW1 | GRCh38.p7 | 7:43180445 | CTGTCGCCCAGGCTG[C/G]AGTGCAGTGGTGCGA | 23072 |
rs10215160 | snp | C/T | 0.331642 | 0.236293 | intron-variant | HECW1 | GRCh38.p7 | 7:43180585 | tatttttagtagaga[C/T]ggggtttcaccgtgt | 23072 |
rs10215185 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43497461 | CATCTGTGTTTTTAG[C/T]GACCACAGATGCAAT | 23072 |
rs10215321 | snp | A/C | 0.306431 | 0.243548 | intron-variant | HECW1 | GRCh38.p7 | 7:43182390 | atccagttttcccag[A/C]cccatttactgaaaa | 23072 |
rs10215485 | snp | C/T | 0.331642 | 0.236293 | intron-variant | HECW1 | GRCh38.p7 | 7:43180572 | ggctaattttttgta[C/T]ttttagtagagacgg | 23072 |
rs10215924 | snp | C/G | 0.496483 | 0.0417852 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43158975 | CCAGAGGTTCTGATT[C/G]AGTAGGTGGGAAAGG | 23072 |
rs10216035 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43182422 | attgtcctttcccca[A/G]tgtgtgtttttggtc | 23072 |
rs10216152 | snp | A/G | 0.485049 | 0.0851591 | intron-variant | HECW1 | GRCh38.p7 | 7:43390145 | CTCGTAGTGATTAGC[A/G]TAAGAGCCCTGAAAT | 23072 |
rs10224012 | snp | A/C | 0.412917 | 0.189626 | intron-variant | HECW1 | GRCh38.p7 | 7:43391560 | AGCCCCTTTGTTGGG[A/C]CTTCTTAGTCTTTAT | 23072 |
rs10224940 | snp | C/T | 0.121369 | 0.214369 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43138285 | CAACTTACATTTTCT[C/T]GGCTTATGTAGTCAA | 23072 |
rs10225160 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43480017 | AACTGAAAATGCACT[G/T]TCAGGAGATCCCTAC | 23072 |
rs10225325 | snp | A/G | 0.160938 | 0.233598 | intron-variant | HECW1 | GRCh38.p7 | 7:43291494 | tatcttggttaaagt[A/G]caaggacatagaatg | 23072 |
rs10225452 | snp | G/T | 0.427879 | 0.175668 | intron-variant | HECW1 | GRCh38.p7 | 7:43430396 | AGCAGATCAAGTTAG[G/T]AAAAATTGCAAAGTT | 23072 |
rs10225907 | snp | C/T | 0.11963 | 0.213316 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160005 | AATATAGTACATACA[C/T]TATTTTCTTGTTTAT | 23072 |
rs10226241 | snp | A/G | 0.286303 | 0.24735 | intron-variant | HECW1 | GRCh38.p7 | 7:43535114 | CTAACATCAGACCTT[A/G]TGATATCATCCTCCA | 23072 |
rs10226549 | snp | C/T | 0.392325 | 0.205532 | intron-variant | HECW1 | GRCh38.p7 | 7:43163692 | GATCAACTAAGCTCC[C/T]CCAAATGGCTCTGCT | 23072 |
rs10227279 | snp | G/T | 0.469937 | 0.118861 | intron-variant | HECW1 | GRCh38.p7 | 7:43395802 | CTGTGAGCCCTGTGA[G/T]GCCCAGTCATTACTC | 23072 |
rs10227288 | snp | C/T | 0.377187 | 0.215229 | intron-variant | HECW1 | GRCh38.p7 | 7:43455993 | GTGACAGAGCAAGAC[C/T]CTGTCTCAAAAAGAA | 23072 |
rs10227702 | snp | A/C | 0.379158 | 0.214052 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43151506 | ATTTTTAAAATAAAA[A/C]TTGAAGAACATCTCA | 23072 |
rs10228628 | snp | A/G | 0.151668 | 0.229849 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518141 | AAATGAACTCAAGAA[A/G]CCTTGAGTGGTAGAG | 23072 |
rs10229386 | snp | G/T | 0.215747 | 0.247642 | intron-variant | HECW1 | GRCh38.p7 | 7:43204423 | TGGCAGTTAAAGGAT[G/T]CAACTCACTATCAGA | 23072 |
rs10229477 | snp | A/G | 0.421368 | 0.182025 | intron-variant | HECW1 | GRCh38.p7 | 7:43481212 | CCCAGTTCAACATGC[A/G]TAGTCTCCCTCCCTG | 23072 |
rs10231428 | snp | G/T | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126092 | tttttttttttttGG[G/T]TTTTACTCACCACTG | 23072 |
rs10231619 | snp | C/T | 0.492386 | 0.0612297 | intron-variant | HECW1 | GRCh38.p7 | 7:43280995 | TGTTTGGGGCTGTTT[C/T]TCCCCCCATGAAAAT | 23072 |
rs10232294 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43187871 | ACTAAAAAGTGATAT[A/G]CTACAGCACAAGTCA | 23072 |
rs10232587 | snp | A/G | 0.49681 | 0.0398085 | intron-variant | HECW1 | GRCh38.p7 | 7:43454058 | TGTTTGGCTTACTAC[A/G]CTTTTCCATGAGGAA | 23072 |
rs10232976 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43481897 | AGGCTGAGGCGTGAA[C/T]CCGGGAGGCAGAGCT | 23072 |
rs10233484 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HECW1 | GRCh38.p7 | 7:43256684 | ATCATGGTGAAATAC[A/T]GGAATAATTAATAAG | 23072 |
rs10235359 | snp | A/C | 0.127599 | 0.217986 | intron-variant | HECW1 | GRCh38.p7 | 7:43436895 | tttgagatggagtct[A/C]actctgtcacccagg | 23072 |
rs10235629 | snp | C/G | 0.206029 | 0.246103 | intron-variant | HECW1 | GRCh38.p7 | 7:43437112 | AGCCCACTTCCTGGA[C/G]TTCAGTTTGGAGCAT | 23072 |
rs10237187 | snp | C/G | 0.183886 | 0.241099 | intron-variant | HECW1 | GRCh38.p7 | 7:43277086 | GTCCTCCTCTTCTTT[C/G]TCTATCTAATGTAAG | 23072 |
rs10238217 | snp | C/T | 0.322483 | 0.239262 | intron-variant | HECW1 | GRCh38.p7 | 7:43403611 | GCTCAAAATAATCCT[C/T]ATGCCAAAGTCACAG | 23072 |
rs10238504 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | HECW1 | GRCh38.p7 | 7:43538020 | AGAGTGGTCCTTGCT[A/G]CAAAGTGGTCCTTGC | 23072 |
rs10239727 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43488416 | aatgaaagaaagaga[A/G]agagagaaagaaaga | 23072 |
rs10239801 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160202 | TTTGTCATTTGTTTT[A/G]TAATTTAAGATATCC | 23072 |
rs10240214 | snp | C/G | 0.433527 | 0.169758 | intron-variant | HECW1 | GRCh38.p7 | 7:43488807 | CAGTACCAACCAACC[C/G]TTTGCAGACATTTCT | 23072 |
rs10240460 | snp | C/T | 0.495855 | 0.045338 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43510112 | AAACGTGCCCTTTGT[C/T]GCCCCAGAACTTGTG | 23072 |
rs10241614 | snp | A/G | 0.418169 | 0.184985 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514041 | GCCAAACCCAACCAT[A/G]AACCAGAGGACAGAG | 23072 |
rs10242062 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | HECW1 | GRCh38.p7 | 7:43288310 | GACACTGTCAAAATC[C/T]GGGAGCAGGGAGGGA | 23072 |
rs10242285 | snp | A/G | 0.146314 | 0.227484 | intron-variant | HECW1 | GRCh38.p7 | 7:43288339 | GAGGAAGGTGGCCAT[A/G]TGTATTTGAAAAAAA | 23072 |
rs10242568 | snp | A/G | | | intron-variant, downstream-variant-500B | HECW1, LOC102724903 | GRCh38.p7 | 7:43296070 | ATATTATAAATATTC[A/G]TGTGTTAAAATGTTA | 23072 |
rs10243459 | snp | A/G | 0.493386 | 0.0571263 | intron-variant | HECW1 | GRCh38.p7 | 7:43289256 | GGATTACAGGCATGT[A/G]CCACCACGCCCAGCT | 23072 |
rs10243801 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43188599 | ATGTTGGAGGTGTTT[C/T]CTTGCTGGCTCATAG | 23072 |
rs10244157 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43188751 | GAGACTCCTGCCCCC[A/G]TGCCATATCTGGCCA | 23072 |
rs10244628 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | HECW1 | GRCh38.p7 | 7:43275195 | caacaaaaagtttac[C/T]tgaaatcctatttag | 23072 |
rs10244850 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | HECW1 | GRCh38.p7 | 7:43264594 | ctcacgcctgtaatc[C/T]cagcactttgggagg | 23072 |
rs10245177 | snp | A/T | 0.282105 | 0.24793 | intron-variant | HECW1 | GRCh38.p7 | 7:43426887 | GAATGTTTTCATAGT[A/T]ATATACCCAAAATAT | 23072 |
rs10245347 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43484750 | TGAAAGCAGTTATTA[C/T]GAATATAGGATTTAT | 23072 |
rs10245364 | snp | G/T | 0.483199 | 0.0901004 | intron-variant | HECW1 | GRCh38.p7 | 7:43380535 | gtgaatgtatgtgat[G/T]ttttccccctagatg | 23072 |
rs10245574 | snp | A/G | 0.451732 | 0.147663 | intron-variant | HECW1 | GRCh38.p7 | 7:43544922 | GTTTTAAGAGAAAAA[A/G]GATAGTGAAGAACAG | 23072 |
rs10246139 | snp | A/G | 0.494896 | 0.0502606 | intron-variant | HECW1 | GRCh38.p7 | 7:43502333 | TCCATTCCAAGTGAG[A/G]GAATACATATGTTGA | 23072 |
rs10246620 | snp | A/G | 0.287346 | 0.247195 | intron-variant | HECW1 | GRCh38.p7 | 7:43384513 | GTCCATAGGAAAAAA[A/G]ATGTTACATTAGCAA | 23072 |
rs10246645 | snp | C/T | 0.49423 | 0.0534032 | intron-variant | HECW1 | GRCh38.p7 | 7:43289637 | TGGCCCATAGGTGGT[C/T]TTATTAACAGAAGAA | 23072 |
rs10246992 | snp | A/G | 0.15698 | 0.23205 | intron-variant | HECW1 | GRCh38.p7 | 7:43289755 | aagtgtggcccaggt[A/G]gttacagtttggttt | 23072 |
rs10247622 | snp | A/G | 0.342134 | 0.232404 | intron-variant | HECW1 | GRCh38.p7 | 7:43402459 | CTCTCCTATTTCACA[A/G]GTTCTAAGGGGAGAA | 23072 |
rs10248955 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43184422 | tatatagCtgtgata[C/T]tatgaaatatgtatt | 23072 |
rs10250324 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43486193 | ccctgccaaggacac[A/G]aactcatcctttatt | 23072 |
rs10250351 | snp | A/G | 0.413416 | 0.189196 | intron-variant | HECW1 | GRCh38.p7 | 7:43202500 | TTTTTTTGAAACAGA[A/G]TCTCACTCTATCCCC | 23072 |
rs10250916 | snp | G/T | 0.209084 | 0.246629 | intron-variant | HECW1 | GRCh38.p7 | 7:43281593 | CAGCTCTTCTTTCTC[G/T]CAGTCCACTCTCCCT | 23072 |
rs10251401 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43416147 | gttctgttttttccc[C/G]atctttgtggtttta | 23072 |
rs10251643 | snp | C/T | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43315410 | TTCTACATCATTGGC[C/T]TAGTAGTAAGAAAGA | 23072 |
rs10251744 | snp | A/C | 0.236144 | 0.249616 | intron-variant | HECW1 | GRCh38.p7 | 7:43308332 | ttatatgatatattt[A/C]tatatattatatgat | 23072 |
rs10251772 | snp | A/G | 0.279195 | 0.248289 | intron-variant | HECW1 | GRCh38.p7 | 7:43315380 | AGAGTTCCTGCTTCT[A/G]CAAGAGAATGGCGCT | 23072 |
rs10252555 | snp | A/G | 0.118235 | 0.212457 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157477 | ACCATTGCTGTACTC[A/G]TAGAATAATAAATTA | 23072 |
rs10253174 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43185534 | gtgtcagaattgaat[C/T]ggaggacacccagct | 23072 |
rs10253450 | snp | A/G | 0.480539 | 0.0967035 | intron-variant | HECW1 | GRCh38.p7 | 7:43451506 | CCTGGTAACTGTAGT[A/G]GGTAATTAATAATTA | 23072 |
rs10253699 | snp | C/G | 0.41325 | 0.18934 | intron-variant | HECW1 | GRCh38.p7 | 7:43391546 | GTGTTGCTTTCCCCA[C/G]CCCCTTTGTTGGGAC | 23072 |
rs10253913 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43120978 | CCCTAAAAGCTGCTG[G/T]ATTAGAGTTTAGATG | 23072 |
rs10253986 | snp | A/G | 0.300169 | 0.244914 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509958 | ATAGTTTGGCTATAG[A/G]GCATCAGTATAACCC | 23072 |
rs10254147 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43186088 | GCTCAAAGATCAAGA[A/G]CAAGATAATCGTCAT | 23072 |
rs10254443 | snp | C/G | 0.030665 | 0.119967 | intron-variant | HECW1 | GRCh38.p7 | 7:43351440 | tctcaagattatatg[C/G]cctttatcttccact | 23072 |
rs10254482 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115428 | TCCAACCCCATCTTA[A/G]ATAATTGAGAATTCA | 23072 |
rs10254921 | snp | C/T | 0.425586 | 0.17796 | intron-variant | HECW1 | GRCh38.p7 | 7:43291630 | tatttctaacactta[C/T]gatttattcttcaac | 23072 |
rs10255363 | snp | G/T | 0.493107 | 0.0583 | intron-variant | HECW1 | GRCh38.p7 | 7:43447134 | CTTTGTGGGTCAAGA[G/T]GTAAAAAGCTAAATA | 23072 |
rs10255565 | snp | C/T | 0.380138 | 0.213458 | intron-variant | HECW1 | GRCh38.p7 | 7:43408191 | CAGTAAGCCCTAAAA[C/T]ATCCCTGGTTGGGTT | 23072 |
rs10256331 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43492392 | CCTCCTCACCTATCT[A/G]TTCCCCTCCCTGTCT | 23072 |
rs10256411 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43483521 | GGACCACAGCTCAGG[A/T]TTCCTAACAGTCATC | 23072 |
rs10256518 | snp | C/T | 0.313326 | 0.241847 | intron-variant | HECW1 | GRCh38.p7 | 7:43307917 | atatatatatatata[C/T]acaCACACACatata | 23072 |
rs10256689 | snp | A/T | 0.455144 | 0.142885 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513863 | AAAGAGAAAGAGGAG[A/T]TAGAGTCAGAAGAGC | 23072 |
rs10257003 | snp | C/T | 0.420255 | 0.183066 | intron-variant | HECW1 | GRCh38.p7 | 7:43388900 | CCAGGTAAGAATGAT[C/T]GGCCTACAGAGGGTG | 23072 |
rs10257024 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43287187 | gagaaataatacagg[A/G]aatagggaaagagag | 23072 |
rs10257742 | snp | G/T | 0.193028 | 0.243422 | intron-variant | HECW1 | GRCh38.p7 | 7:43422593 | AGGCTGGTCTTGAAC[G/T]CCTGATGTCAGATGA | 23072 |
rs10257823 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43517910 | GTCCTATTTCTGAAC[C/G]CAGCTTTCTTCAGAA | 23072 |
rs10257851 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | HECW1 | GRCh38.p7 | 7:43548061 | gttatgatttaatac[C/T]gcattttgatgtttg | 23072 |
rs10258153 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | HECW1 | GRCh38.p7 | 7:43422936 | GCCTGGCCGAGAGTC[A/G]TGGTCTCCAGGATTT | 23072 |
rs10258168 | snp | C/G | 0.332337 | 0.236052 | intron-variant | HECW1 | GRCh38.p7 | 7:43453065 | tgtaaatcacttaag[C/G]gcttttactctgaac | 23072 |
rs10258192 | snp | A/G | 0.151334 | 0.229706 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518070 | AATGAAATTTCTTCA[A/G]GAAAATCTAGGTGAA | 23072 |
rs10259850 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | HECW1 | GRCh38.p7 | 7:43293122 | ctactctggaggctg[A/G]ggcagaagaatcgct | 23072 |
rs10260214 | snp | A/G | 0.499885 | 0.00758699 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523311 | TGCCTGGCCTTGCTC[A/G]TATTTTTAAACACCA | 23072 |
rs10261111 | snp | A/G | 0.303187 | 0.244277 | intron-variant | HECW1 | GRCh38.p7 | 7:43398861 | AGTGCTGATTGGTTG[A/G]GTTGAAGATGAAATC | 23072 |
rs10261180 | snp | G/T | 0.202651 | 0.245475 | intron-variant | HECW1 | GRCh38.p7 | 7:43193121 | attgctatggcattt[G/T]taaactgtcatgatg | 23072 |
rs10261813 | snp | A/G | 0.422787 | 0.180679 | intron-variant | HECW1 | GRCh38.p7 | 7:43393431 | ACATGCTTCTGCAAC[A/G]CATCTCGAGTGAGAA | 23072 |
rs10261826 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43328612 | AGGATTCCATTGCAT[C/T]TGGGGGACATCAAAA | 23072 |
rs10262152 | snp | C/T | 0.497613 | 0.0344622 | intron-variant | HECW1 | GRCh38.p7 | 7:43289638 | GGCCCATAGGTGGTC[C/T]TATTAACAGAAGAAC | 23072 |
rs10263551 | snp | A/C | 0.200492 | 0.245049 | intron-variant | HECW1 | GRCh38.p7 | 7:43165314 | AGCCATGTGCATACA[A/C]TTTCCAACTTTAGAA | 23072 |
rs10263679 | snp | A/G | 0.203882 | 0.245709 | intron-variant | HECW1 | GRCh38.p7 | 7:43165430 | TGTGTGCACACAGGT[A/G]TGTGTGTGTGTTTGA | 23072 |
rs10263879 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43499791 | AGTAACATCAGGGAA[A/G]CAAATTAAAAAGTTA | 23072 |
rs10263891 | snp | A/T | 0.283947 | 0.247685 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520981 | GCAGCACCCTTCAGG[A/T]CCTGAGGCAGGTGCC | 23072 |
rs10264353 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | HECW1 | GRCh38.p7 | 7:43281478 | AACCTGTTATTCAGA[A/G]GTTGTGCAATATCAC | 23072 |
rs10264397 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43500203 | CCTCCCGGTTCAAGC[A/G]ATTCTCCTACCTCAG | 23072 |
rs10264595 | snp | C/T | 0.255224 | 0.249945 | intron-variant | HECW1 | GRCh38.p7 | 7:43420441 | cactttagccacttc[C/T]gtttaatattgtgct | 23072 |
rs10264623 | snp | C/G | 0.416708 | 0.186302 | intron-variant | HECW1 | GRCh38.p7 | 7:43193724 | gactgcctttccctg[C/G]cactggctgtgacca | 23072 |
rs10264725 | snp | A/G | 0.490727 | 0.0674567 | intron-variant | HECW1 | GRCh38.p7 | 7:43406889 | CCACCACTGCACTTC[A/G]GCCTGGGTGACTCCA | 23072 |
rs10265829 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | HECW1 | GRCh38.p7 | 7:43320377 | taattatttctctgt[C/T]tctggaggtgttcca | 23072 |
rs10266995 | snp | C/T | 0.28052 | 0.24813 | intron-variant | HECW1 | GRCh38.p7 | 7:43315296 | TCCAAAGAAACAATA[C/T]GAAGGAAAGGCCACA | 23072 |
rs10267325 | snp | A/G | 0.495927 | 0.0449436 | intron-variant | HECW1 | GRCh38.p7 | 7:43354676 | tagaaaattacctca[A/G]aagaccaaatctaag | 23072 |
rs10268328 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | HECW1 | GRCh38.p7 | 7:43531283 | cccgccagagccaag[C/T]tatgcttcctccccg | 23072 |
rs10268495 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HECW1 | GRCh38.p7 | 7:43555334 | TGTGGAAAAGGAGAC[A/G]CTGGGGCTCCAGGCA | 23072 |
rs10268777 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43185555 | acacccagctagtgt[C/T]tgctagagaatcccc | 23072 |
rs10269200 | snp | C/G | 0.11963 | 0.213316 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159904 | CAGGATGGTCTCGAT[C/G]TCCTGACCTCGTGAT | 23072 |
rs10269221 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159959 | GCTGCGATTACAGGC[A/G]TGAGCCACCGCGCCC | 23072 |
rs10269274 | snp | C/T | 0.115438 | 0.210697 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43160156 | TGTGGGTGGCATCTT[C/T]GTGATCTTTGCCCAT | 23072 |
rs10269585 | snp | A/C | 0.497558 | 0.0348586 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43154479 | TTTGCATTTCTAGGT[A/C]GTGAAAGTTTCCTCC | 23072 |
rs10270105 | snp | A/G | 0.330249 | 0.23677 | intron-variant | HECW1 | GRCh38.p7 | 7:43455499 | CCACTGAACCTAATC[A/G]CCCTCTGTTAGACTT | 23072 |
rs10270335 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | HECW1 | GRCh38.p7 | 7:43455692 | AGAATTTTTGTATTC[A/G]TCACACCATCACACC | 23072 |
rs10270388 | snp | C/G | 0.47852 | 0.101384 | intron-variant | HECW1 | GRCh38.p7 | 7:43395718 | AGCCAAGCTCACAGG[C/G]TCACCAGGGGCACCT | 23072 |
rs10270458 | snp | A/G | 0.485596 | 0.0836329 | intron-variant | HECW1 | GRCh38.p7 | 7:43395594 | GCCGAGCCCCATTCC[A/G]TATGTCACTCCACTG | 23072 |
rs10270508 | snp | A/G | 0.449345 | 0.150869 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513850 | TAATATTCAGGCCAA[A/G]GAGAAAGAGGAGTTA | 23072 |
rs10270514 | snp | A/G | 0.421842 | 0.181577 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43513855 | TTCAGGCCAAAGAGA[A/G]AGAGGAGTTAGAGTC | 23072 |
rs10270998 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514187 | CCTCTACATTTCAGG[A/G]CATTCAACCCATCCA | 23072 |
rs10271015 | snp | A/G | 0.420733 | 0.18262 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514231 | AATTTACAGAACAGT[A/G]TGTGTCTGTTGTGTC | 23072 |
rs10271615 | snp | A/T | 0.472052 | 0.11486 | intron-variant | HECW1 | GRCh38.p7 | 7:43383551 | atgatgagctttttt[A/T]catatgtttattggc | 23072 |
rs10271714 | snp | A/G | 0.472147 | 0.114677 | intron-variant | HECW1 | GRCh38.p7 | 7:43383593 | cttcttttgagaagc[A/G]tctgttcatatcctt | 23072 |
rs10271819 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43260740 | aagtcataggactta[C/G]tcattgcttggatgt | 23072 |
rs10272239 | snp | A/G | 0.20111 | 0.245173 | intron-variant | HECW1 | GRCh38.p7 | 7:43167495 | AACAACTCCAGATGG[A/G]GGGAGGTTGGAAGAG | 23072 |
rs10272268 | snp | C/T | 0.495016 | 0.0496707 | intron-variant | HECW1 | GRCh38.p7 | 7:43287004 | CCGGGCATTGTTTAA[C/T]GATGGTTGGGGGTAG | 23072 |
rs10272524 | snp | A/G | 0.039522 | 0.134904 | intron-variant | HECW1 | GRCh38.p7 | 7:43167747 | AGTTCTAGTTCAAGT[A/G]CCACCCTCTCTCCTG | 23072 |
rs10272651 | snp | A/G | 0.140242 | 0.224618 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137779 | ggtctcgaactcctg[A/G]gctcaagtgatctgc | 23072 |
rs10272674 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43225488 | agcaaaataaaaaaa[A/C]tggaaacaacctaaa | 23072 |
rs10272727 | snp | G/T | 0.435263 | 0.167862 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43523241 | AACTCCTGACCTCAG[G/T]TGATTCACCTGCCTC | 23072 |
rs10272828 | snp | A/C | 0.116488 | 0.211364 | intron-variant | HECW1 | GRCh38.p7 | 7:43255715 | aggtgcaggagatga[A/C]atgatgagccaagcc | 23072 |
rs10272919 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43218557 | CACAGTGTGCCTGTG[A/T]CCAGCAGTATAGATC | 23072 |
rs10273324 | snp | A/G | 0.453209 | 0.145623 | intron-variant | HECW1 | GRCh38.p7 | 7:43371434 | TGTGCTTTCTGCTCA[A/G]TTTTGCTGTGGACCT | 23072 |
rs10273734 | snp | C/T | 0.152334 | 0.230133 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518082 | TCAGGAAAATCTAGG[C/T]GAATTTATGCATATG | 23072 |
rs10273874 | snp | G/T | 0.42263 | 0.180829 | intron-variant | HECW1 | GRCh38.p7 | 7:43432080 | TGATCTACCCACCTC[G/T]GCCTTCCAAAGTGCT | 23072 |
rs10273924 | snp | C/T | 0.289424 | 0.246872 | intron-variant | HECW1 | GRCh38.p7 | 7:43432284 | agctgggactacagg[C/T]gcccgccactacacc | 23072 |
rs10273982 | snp | C/T | 0.464523 | 0.128375 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43518242 | GCTCACACCTCTAAT[C/T]CCAACACTTTAGGAG | 23072 |
rs10274010 | snp | A/G | 0.438666 | 0.164028 | intron-variant | HECW1 | GRCh38.p7 | 7:43432183 | CTCGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 23072 |
rs10274221 | snp | A/G | 0.420892 | 0.182472 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43514392 | cctcctggttcaagc[A/G]agtctcctgcctcag | 23072 |
rs10274398 | snp | G/T | 0.282369 | 0.247896 | intron-variant | HECW1 | GRCh38.p7 | 7:43352490 | AAGTGGAAGTTTACT[G/T]CTGTTAGCTGGTCAG | 23072 |
rs10274944 | snp | A/G | 0.473634 | 0.111748 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126048 | ATGCAAGGCGTGCGT[A/G]TATATGAGTTTGTTC | 23072 |
rs10274988 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43361942 | aggtcaggagtttaa[A/G]accagcctggccaac | 23072 |
rs10275087 | snp | G/T | 0.440333 | 0.16209 | intron-variant | HECW1 | GRCh38.p7 | 7:43427002 | ATCTGATGCCTTGAT[G/T]TATTATTATAATCTA | 23072 |
rs10275172 | snp | A/G | 0.49306 | 0.0584955 | intron-variant | HECW1 | GRCh38.p7 | 7:43184230 | gtgttagccaggatg[A/G]tctcgatctcctgac | 23072 |
rs10275175 | snp | A/G | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43126270 | TCTTCCCCACCACTA[A/G]AAAAATTCCTCTCTT | 23072 |
rs10276071 | snp | C/G | 0.453697 | 0.14494 | intron-variant | HECW1 | GRCh38.p7 | 7:43502457 | AGCCCAAGAGTTCGA[C/G]ACCAGCCTGGGCCAT | 23072 |
rs10276567 | snp | G/T | 0.490231 | 0.0692021 | intron-variant | HECW1 | GRCh38.p7 | 7:43357281 | ctgcactcccatgtt[G/T]attgcagtactgatc | 23072 |
rs10276639 | snp | G/T | 0.496616 | 0.0409947 | intron-variant | HECW1 | GRCh38.p7 | 7:43288158 | TTCTCTAGGGCTTTT[G/T]CAATTAAACACACAG | 23072 |
rs10276793 | snp | C/G | 0.084364 | 0.187256 | intron-variant | HECW1 | GRCh38.p7 | 7:43462294 | AGGAGCCCCCAGCTG[C/G]TCTCCACAGCTCCCA | 23072 |
rs10276805 | snp | C/T | 0.084728 | 0.187577 | intron-variant | HECW1 | GRCh38.p7 | 7:43462314 | CACAGCTCCCAGCTC[C/T]TCTCCTCCAGTGCAT | 23072 |
rs10277317 | snp | C/T | 0.248471 | 0.249995 | intron-variant | HECW1 | GRCh38.p7 | 7:43372478 | CACCCATTAACTCGT[C/T]GTTTTCATTAGGTAT | 23072 |
rs10277619 | snp | A/G | 0.416382 | 0.186593 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161953 | CTTGCGCCTTTCACC[A/G]CCCACTATTGAACAT | 23072 |
rs10277623 | snp | A/G | 0.402277 | 0.198272 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161963 | TCACCGCCCACTATT[A/G]AACATGCAGATGTGA | 23072 |
rs10277708 | snp | G/T | 0.306431 | 0.243548 | intron-variant | HECW1 | GRCh38.p7 | 7:43187904 | CCCAGACTGAATTTT[G/T]TCACATGTGCAACCA | 23072 |
rs10278218 | snp | C/T | 0.498323 | 0.0289051 | intron-variant | HECW1 | GRCh38.p7 | 7:43373122 | GGCAAAGCAGACTAA[C/T]GGTGCTGGGAGTCAC | 23072 |
rs10278689 | snp | C/T | 0.413914 | 0.188765 | intron-variant | HECW1 | GRCh38.p7 | 7:43427763 | cattcaggttgttgg[C/T]agaattgagatcctt | 23072 |
rs10279129 | snp | C/T | 0.390277 | 0.206936 | intron-variant | HECW1 | GRCh38.p7 | 7:43168616 | AGTAAGCTGTGATTG[C/T]ACCACTACACTTCAG | 23072 |
rs10279340 | snp | C/T | 0.490231 | 0.0692021 | intron-variant | HECW1 | GRCh38.p7 | 7:43357383 | aatagtattcagtca[C/T]aaaaaagaatggaat | 23072 |
rs10279680 | snp | C/G | 0.399968 | 0.200024 | intron-variant | HECW1 | GRCh38.p7 | 7:43327547 | TAATTCCCCTCCCTG[C/G]TGTCCCTACCACCTA | 23072 |
rs10279975 | snp | C/T | 0.283684 | 0.24772 | intron-variant | HECW1 | GRCh38.p7 | 7:43429333 | ATATATATATATATA[C/T]ATACATATATGCAGA | 23072 |
rs10279979 | snp | C/T | 0.418653 | 0.184544 | intron-variant | HECW1 | GRCh38.p7 | 7:43429335 | ATATATATATATATA[C/T]ACATATATGCAGATT | 23072 |
rs10280153 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | HECW1 | GRCh38.p7 | 7:43408337 | CCCTTCTCCACTCCT[A/G]AAAGTGTTGCCTTTG | 23072 |
rs10280162 | snp | A/G | 0.287867 | 0.247116 | intron-variant | HECW1 | GRCh38.p7 | 7:43385731 | CAGATATTTCTCCCA[A/G]GGCAAAAGAATATGT | 23072 |
rs10280235 | snp | A/G | 0.494484 | 0.0522255 | intron-variant | HECW1 | GRCh38.p7 | 7:43202610 | TCCTGAGGAGCTGGG[A/G]TTACAGGCACCTGCC | 23072 |
rs10280809 | snp | A/G | 0.482683 | 0.0914256 | intron-variant | HECW1 | GRCh38.p7 | 7:43386206 | GCCCAGATTGAAAGA[A/G]TTTGTGTGATTCAGT | 23072 |
rs10281361 | snp | G/T | 0.48666 | 0.0805725 | intron-variant | HECW1 | GRCh38.p7 | 7:43394327 | TGGGAATAACAGACA[G/T]AAAGGAGGAGGGAGA | 23072 |
rs10281533 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HECW1 | GRCh38.p7 | 7:43491499 | AGGCGTACCTTACCA[A/G]TGATATTTATCTAGG | 23072 |
rs10281626 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | HECW1 | GRCh38.p7 | 7:43250941 | CTTCAGATCCTCACA[A/G]CTCCTACTTAGCTCA | 23072 |
rs10281837 | snp | C/G | 0.430136 | 0.173352 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132894 | TGTGGTGAAAGAAGA[C/G]TTCTATTTAGTTCTT | 23072 |
rs10281930 | snp | A/C | 0.497558 | 0.0348586 | intron-variant | HECW1 | GRCh38.p7 | 7:43373822 | GGAGCCCTTGGCAGC[A/C]ACCATCCTACTTCCT | 23072 |
rs10282004 | snp | C/T | 0.478685 | 0.10101 | intron-variant | HECW1 | GRCh38.p7 | 7:43394852 | ttactcaaatccatc[C/T]cccggagcattcagg | 23072 |
rs10282127 | snp | A/G | 0.498277 | 0.0293024 | intron-variant | HECW1 | GRCh38.p7 | 7:43373785 | CCCCACTAAACACCA[A/G]CTCCTCATTCTCCCC | 23072 |
rs10282382 | snp | A/G | 0.473543 | 0.111932 | intron-variant | HECW1 | GRCh38.p7 | 7:43373985 | TTCCTCCCTTTTTAA[A/G]GCTGAATAGTATTCC | 23072 |
rs10282502 | snp | C/T | 0.117537 | 0.212022 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43157774 | ccgcattgcccaggc[C/T]ggtcttaatctcctg | 23072 |
rs10282609 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | HECW1 | GRCh38.p7 | 7:43451503 | TCTCCTGGTAACTGT[A/G]GTGGGTAATTAATAA | 23072 |
rs10464374 | snp | G/T | 0.201418 | 0.245234 | intron-variant | HECW1 | GRCh38.p7 | 7:43179968 | CCTTTGCTTTATCTG[G/T]GGAGGGTAAAATAAT | 23072 |
rs10464376 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43180387 | ATTTTATTATTTTAt[A/T]tttttatttgtattt | 23072 |
rs10480183 | snp | C/G | 0.41408 | 0.188621 | intron-variant | HECW1 | GRCh38.p7 | 7:43426123 | GCCCCAATTATTGAC[C/G]AATCATGGGGCACTT | 23072 |
rs10480184 | snp | A/G | 0.192715 | 0.243348 | intron-variant | HECW1 | GRCh38.p7 | 7:43431281 | CTTCTATCCTTCCAT[A/G]CCCAGGCCTCTATTT | 23072 |
rs10486733 | snp | A/C | 0.49621 | 0.0433651 | intron-variant | HECW1 | GRCh38.p7 | 7:43233525 | CATCCAGGAAAATCT[A/C]TCATCGGCCTGCTAA | 23072 |
rs10486736 | snp | A/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43188385 | TGTTGGGTAAATAAC[A/T]CTGAATTTCCTTGAT | 23072 |
rs10486737 | snp | C/T | 0.306679 | 0.24349 | intron-variant | HECW1 | GRCh38.p7 | 7:43188049 | CCTGTCATCAGGACA[C/T]TTGTTATGTTTGTGC | 23072 |
rs10486738 | snp | A/G | 0.333261 | 0.235728 | intron-variant | HECW1 | GRCh38.p7 | 7:43187956 | ACGGAGTCCACTGAT[A/G]GGACATTCAGCCATT | 23072 |
rs10486739 | snp | C/T | 0.306679 | 0.24349 | intron-variant | HECW1 | GRCh38.p7 | 7:43187753 | CAGAACCTATTTGGT[C/T]GAATTGGGTGAGAAG | 23072 |
rs10487674 | snp | A/G | 0.273049 | 0.248935 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43522215 | TCCAATAATCAGAGA[A/G]GTCTAATATGTGAGT | 23072 |
rs10487675 | snp | C/G | 0.456095 | 0.141508 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43521101 | AGGCACTCTTATGTC[C/G]TTTTGGTGAACTAGG | 23072 |
rs10487676 | snp | C/T | 0.190205 | 0.242744 | intron-variant | HECW1 | GRCh38.p7 | 7:43496166 | TTTTTCCAATTCCAA[C/T]GTGGCCTGATTTCAA | 23072 |
rs10487678 | snp | A/G | 0.227369 | 0.248974 | intron-variant | HECW1 | GRCh38.p7 | 7:43460114 | TATAAGGCAATCTTA[A/G]TATTTAGCAGGCCCT | 23072 |
rs10487680 | snp | A/C | 0.0919752 | 0.193722 | intron-variant | HECW1 | GRCh38.p7 | 7:43396184 | TTTCATCATTGCTCA[A/C]TATTTAGTAATAGGT | 23072 |
rs10562074 | in-del | -/TGTGTGTG | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43317810 | CTTTTTTCTCATTAT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 23072 |
rs10574466 | in-del | -/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43401577 | TTTTTTTTTTTTTTT[-/T]CCCCCCAAATATAGC | 23072 |
rs10591967 | in-del | -/GTGA | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43183803 | TTATTCTTCTGGAAT[-/GTGA]GTAACTATTTTGCTA | 23072 |
rs10602318 | in-del | -/TAAAT | 0.307671 | 0.243257 | intron-variant | HECW1 | GRCh38.p7 | 7:43230894 | AAGATTTAAAAAAAA[-/TAAAT]TAAAGCAGAAAGGGA | 23072 |
rs10604163 | in-del | -/TT | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43319791 | GGCTAATTTTTGTAA[-/TT]TTTTTTTTTTTTTTT | 23072 |
rs10625732 | in-del | -/TATTAT | 0.5 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43327961 | TCTATGAACCATTTA[-/TATTAT]TATTATTATTATTAT | 23072 |
rs10634938 | in-del | -/TATTT | 0.499437 | 0.0167637 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43130865 | GAAATGCTCAACCTG[-/TATTT]TATTAATAACTGGGT | 23072 |
rs10636404 | in-del | -/ATAT | 0.00636936 | 0.0560724 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43161809 | CAGTCCCTAATTCCC[-/ATAT]ATATACACTTCTCTG | 23072 |
rs10643628 | in-del | -/AAAG/AAGA | | | intron-variant | HECW1 | GRCh38.p7 | 7:43268014 | TATCACAGACAAATA[-/AAAG/AAGA]TAGAACACTTGCCAC | 23072 |
rs10647655 | in-del | -/TTAG | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43224669 | ACAGAAAATAAAAAG[-/TTAG]CCGGCCATGGTGGCA | 23072 |
rs10648012 | in-del | -/AC | | | intron-variant | HECW1 | GRCh38.p7 | 7:43250118 | TTTTTTTTAACCAAA[-/AC]ACACACACACACACA | 23072 |
rs10660691 | in-del | -/TT | 0.49263 | 0.0602539 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43147245 | AAGAATGTAGTTTTG[-/TT]TTTTTTTTTAACAGC | 23072 |
rs10677654 | in-del | -/AC | 0.340456 | 0.251208 | intron-variant | HECW1 | GRCh38.p7 | 7:43183970 | ACAATTTAAAAAAAA[-/AC]AATCAAGATGTGATT | 23072 |
rs10695541 | in-del | -/GT/GTGTGT | | | intron-variant | HECW1 | GRCh38.p7 | 7:43262265 | TGTGTGTGTGTGTGT[-/GT/GTGTGT]ATAACCTAAAGAAAT | 23072 |
rs10714582 | in-del | -/A | 0.472335 | 0.114312 | intron-variant | HECW1 | GRCh38.p7 | 7:43305400 | AATCTCAATTACTGC[-/A]ATTCTGTCCATCTGT | 23072 |
rs10807917 | snp | A/G | 0.321292 | 0.23962 | intron-variant | HECW1 | GRCh38.p7 | 7:43539381 | TCTTTAAAAATATGT[A/G]TATCCAGTCCCAGTA | 23072 |
rs10951716 | snp | A/G | 0.193966 | 0.243639 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115651 | GCAGTGTTTTCATGC[A/G]CTATGGTAATTTTTA | 23072 |
rs10951717 | snp | A/G | 0.472335 | 0.114312 | intron-variant | HECW1 | GRCh38.p7 | 7:43209027 | GGCTATATGCACAAA[A/G]CATTACCTCTTATTT | 23072 |
rs10951720 | snp | C/G | 0.487049 | 0.0794222 | intron-variant | HECW1 | GRCh38.p7 | 7:43287085 | GAACGTAACAAAGTC[C/G]TCATGGAATGTACCT | 23072 |
rs10951721 | snp | C/T | 0.494733 | 0.0510469 | intron-variant | HECW1 | GRCh38.p7 | 7:43287096 | AGTCCTCATGGAATG[C/T]ACCTTGTTGTGAGAG | 23072 |
rs10951723 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | HECW1 | GRCh38.p7 | 7:43309654 | GTAAACCTTACAAAT[A/G]AAGGAGCCTCTCCCC | 23072 |
rs10951724 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | HECW1 | GRCh38.p7 | 7:43318207 | AGAGTGGAGAAATTC[A/G]GGGAAATACTATCCC | 23072 |
rs10951725 | snp | A/G | 0.499154 | 0.0205497 | intron-variant | HECW1 | GRCh38.p7 | 7:43337933 | CAACTGCAACTGGGA[A/G]AAGCAACTACCAATT | 23072 |
rs10951726 | snp | G/T | 0.357664 | 0.225629 | intron-variant | HECW1 | GRCh38.p7 | 7:43338194 | TTGTCGTTGGCCTGG[G/T]AGACACTGCTGGGAT | 23072 |
rs10951727 | snp | A/C | 0.176219 | 0.238865 | intron-variant | HECW1 | GRCh38.p7 | 7:43350352 | tgcctaggggaagat[A/C]tttttgtggttaatt | 23072 |
rs10951728 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43374799 | AAAAAAAAAAAAAAA[A/C]ATAGAGAAATATAAT | 23072 |
rs10951730 | snp | A/G | 0.248188 | 0.249993 | intron-variant | HECW1 | GRCh38.p7 | 7:43394271 | GAGGATGTGGTCTCT[A/G]AACTGATGGCTGATC | 23072 |
rs10951731 | snp | A/G | 0.416218 | 0.186739 | intron-variant | HECW1 | GRCh38.p7 | 7:43412179 | tcatgatctacattg[A/G]gttaattttgtacca | 23072 |
rs10951732 | snp | A/G | 0.185788 | 0.241613 | intron-variant | HECW1 | GRCh38.p7 | 7:43430907 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 23072 |
rs10951733 | snp | C/T | 0.32153 | 0.239548 | intron-variant | HECW1 | GRCh38.p7 | 7:43542298 | TATACAATATTTGTT[C/T]TTTTGTGGCTGACTT | 23072 |
rs10951734 | snp | C/T | 0.421684 | 0.181726 | intron-variant | HECW1 | GRCh38.p7 | 7:43558748 | TGCCATCAGGGAGCT[C/T]AGCAGAGAAAATGGC | 23072 |
rs11313461 | in-del | -/G | 0.158632 | 0.232706 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43132285 | CTTTTAATTTTATTT[-/G]TGATGACCTATTGGT | 23072 |
rs11315311 | in-del | -/A | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43173275 | ATGGCTAAGCAGAGG[-/A]AGAATGGTTTTGCTA | 23072 |
rs11325664 | in-del | -/A | 0.202035 | 0.245356 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43152204 | TGCATAATTTCTGGG[-/A]AAAAAAATGTTCAAG | 23072 |
rs11337179 | in-del | -/G | 0.0581099 | 0.160244 | intron-variant | HECW1 | GRCh38.p7 | 7:43526389 | CTAAGTATTCCAGCA[-/G]TTAGCACAGTGCCTT | 23072 |
rs11352876 | in-del | -/A | 0.339656 | 0.233371 | utr-variant-3-prime | HECW1 | GRCh38.p7 | 7:43563868 | AGGGAGACACCATCT[-/A]AAAAAAAAATAAATA | 23072 |
rs11354315 | in-del | -/A | 0.367708 | 0.220556 | intron-variant | HECW1 | GRCh38.p7 | 7:43238390 | CCCTCTGGTGCTCAG[-/A]AATTGGAGTCTGAGG | 23072 |
rs11360449 | in-del | -/T | 0.283158 | 0.247791 | intron-variant | HECW1 | GRCh38.p7 | 7:43254790 | ATGGCTACTCTCTAC[-/T]TTTGAAAACCACAGA | 23072 |
rs11361472 | in-del | -/T | 0.040671 | 0.13668 | intron-variant | HECW1 | GRCh38.p7 | 7:43227288 | ATGGTCATTTTTTTT[-/T]AGGGGTGTGAGTTTA | 23072 |
rs11362924 | in-del | -/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43343268 | TGGGCAACAGTATTC[-/T]TTTTTTTTTTTTTAA | 23072 |
rs11369993 | in-del | -/T | 0.492386 | 0.0612297 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43119704 | TTTGCTCCCTAAACG[-/T]TGCTTCTCTTCTGGT | 23072 |
rs11373110 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43115315 | TTTTTTTTTTTTTTT[-/T]GTCCACTATAGCAAA | 23072 |
rs11379913 | in-del | -/A | 0.479014 | 0.100263 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43376956 | GGTCACACTTTAGTG[-/A]AAAAAAAAAGACTTT | 23072 |
rs11382992 | in-del | -/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43539673 | CCTCTAAGTGCGGAA[-/G]CCACGGGCCCATCAC | 23072 |
rs11385196 | in-del | -/A | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43137527 | ATGCTTTCTGCCTTC[-/A]TTTTATTTATTTATT | 23072 |
rs11394010 | in-del | -/T | 0.368733 | 0.220005 | intron-variant | HECW1 | GRCh38.p7 | 7:43172430 | TAGAGATTTCTAGGA[-/T]TTTTTTTTTCAATAA | 23072 |
rs11397625 | in-del | -/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43455799 | GTTTGAGACCAGCCT[-/G]GCCAACCATGGCCAA | 23072 |
rs11398778 | in-del | -/C | 0.499515 | 0.0155675 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159767 | TCACTGCAAGCTCCG[-/C]CTCCCAGGTTCATGC | 23072 |
rs11398779 | in-del | -/T | 0 | 0 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159697 | TTTTTTTTTTTTTTT[-/T]GAGATGGAATCTTGC | 23072 |
rs11399090 | in-del | -/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43395053 | CAGTTTGTTGATCTT[-/G]GTGGTGCCAGCTGAT | 23072 |
rs11399162 | in-del | -/T | 0.271432 | 0.24908 | intron-variant | HECW1 | GRCh38.p7 | 7:43366172 | TACAGATTCATATAC[-/T]TTGTCAGACCCCCTG | 23072 |
rs11436937 | in-del | -/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43190085 | ACAGCTGTGGAAATT[-/G]TTTGTTGTTGTTGTT | 23072 |
rs11437548 | in-del | -/C | 0.499187 | 0.0201513 | intron-variant | HECW1 | GRCh38.p7 | 7:43536795 | AGCAAACTTCAAAAG[-/C]AGTCCCTGTAAACTC | 23072 |
rs11439004 | in-del | -/A | 0.321053 | 0.23969 | intron-variant | HECW1 | GRCh38.p7 | 7:43537796 | ACAGTTATTTTTTTT[-/A]AAAAAAGCTATGGCT | 23072 |
rs11440570 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HECW1 | GRCh38.p7 | 7:43365458 | GACATGACATTCCCA[-/C]CCCGTGTGGGGCCAT | 23072 |
rs11451295 | in-del | -/G | 0.336017 | 0.234736 | intron-variant | HECW1 | GRCh38.p7 | 7:43165397 | CACTGGGCTTTTGGC[-/G]GGGGGGGGGTGTTTG | 23072 |
rs11453963 | in-del | -/T | 0.490063 | 0.0697833 | intron-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43520620 | TTGAATTATTTTTTT[-/T]ATTATTATTATTCTA | 23072 |
rs11455925 | in-del | -/T/TT | 0.575608 | 0.147085 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43159184 | CCTTTGTTCATTTTC[-/T/TT]TTTTTTTTTATTATT | 23072 |
rs11472107 | in-del | -/CA | 0.409382 | 0.192607 | intron-variant | HECW1 | GRCh38.p7 | 7:43470741 | TCACACACACACACA[-/CA]TAAATGGTCTCAGCA | 23072 |
rs11532707 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43319351 | gagattgcgccactg[C/G]agtccgcagtccggc | 23072 |
rs11533945 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43402011 | TTGGGGAAGGTCGAA[A/G]AGGAGATTGGCCGAG | 23072 |
rs11561871 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43401666 | CTCATGCTAATCTCA[A/G]ACTTGTCTTCTGAGA | 23072 |
rs11760205 | snp | C/T | 0.299158 | 0.245119 | intron-variant | HECW1 | GRCh38.p7 | 7:43363687 | AGGACTGTATTTTCA[C/T]GGGCAATTAGGTTTC | 23072 |
rs11760314 | snp | C/G | 0.493703 | 0.0557558 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509668 | AGAAGATTGGTATCA[C/G]TCAATGCTGTGCAGT | 23072 |
rs11760429 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HECW1 | GRCh38.p7 | 7:43304076 | ACTCAGAGGAAATGC[A/C/G]TGGGCTGCAGTGATT | 23072 |
rs11760767 | snp | A/T | 0.449091 | 0.151204 | intron-variant | HECW1 | GRCh38.p7 | 7:43255241 | AATAGCTGGAGAGAG[A/T]CAAGTACTGTTCCAG | 23072 |
rs11760786 | snp | G/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43534986 | ACTTTTAGCatctta[G/T]cagctgtcctataca | 23072 |
rs11760891 | snp | A/G | 0.213333 | 0.247296 | intron-variant | HECW1 | GRCh38.p7 | 7:43410232 | atttctcaaagttcc[A/G]aagctgggaagtccg | 23072 |
rs11761433 | snp | C/T | 0.470618 | 0.117591 | intron-variant | HECW1 | GRCh38.p7 | 7:43255357 | TAATCCCAGCACTTT[C/T]GGAGGCTGAGGTGGG | 23072 |
rs11761889 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | HECW1 | GRCh38.p7 | 7:43405759 | gaaggtaggagccct[C/G]ctgaaatccaggttt | 23072 |
rs11761948 | snp | C/T | 0.187685 | 0.242109 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43375859 | GATCAAACCATTGTA[C/T]TCCAGCCTGGGTGAC | 23072 |
rs11762154 | snp | A/G | 0.333722 | 0.235565 | intron-variant | HECW1 | GRCh38.p7 | 7:43187849 | ATATCTCCTACCCCA[A/G]AACTACACTAAAAAG | 23072 |
rs11762205 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43275589 | AGGGAGAGTAATGTA[A/G]ATGCAAATGCACTAA | 23072 |
rs11762544 | snp | A/G | 0.214541 | 0.247473 | intron-variant | HECW1 | GRCh38.p7 | 7:43411604 | ctttactatgttcat[A/G]gaattgtctgtttct | 23072 |
rs11762824 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494634 | tcaacctgacaagta[A/G]ctgggactacaggca | 23072 |
rs11763383 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HECW1 | GRCh38.p7 | 7:43442375 | aggggcatctgTATT[C/T]GATAAGGACTTCCTT | 23072 |
rs11763488 | snp | A/G | 0.256619 | 0.249912 | intron-variant | HECW1 | GRCh38.p7 | 7:43259856 | atgtgagtagttgca[A/G]tcctagaataatgag | 23072 |
rs11763732 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43194507 | AAAAAAGAAAGAAAA[A/C]CCATAAGCCTGTGTG | 23072 |
rs11763891 | snp | C/T | 0.495671 | 0.0463237 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509519 | GTGGACACTGGCTTC[C/T]GCATCTTACTGTAAA | 23072 |
rs11764232 | snp | C/T | 0.425277 | 0.178263 | intron-variant | HECW1 | GRCh38.p7 | 7:43543829 | CTACTCATTTAACTT[C/T]CCTGCCATGTACTCA | 23072 |
rs11764255 | snp | A/C | 0.242201 | 0.249878 | intron-variant | HECW1 | GRCh38.p7 | 7:43448866 | TCTGGGAGGTTCTGG[A/C]GGGTTTCAACACTTG | 23072 |
rs11764295 | snp | C/T | 0.322245 | 0.239334 | intron-variant | HECW1 | GRCh38.p7 | 7:43544039 | CTAAATAAATTCCAG[C/T]TGGATCAGAAACCTG | 23072 |
rs11764328 | snp | C/G | 0.425432 | 0.178112 | intron-variant | HECW1 | GRCh38.p7 | 7:43544134 | TGCTGATACAGATAT[C/G]GCACAAATTCTCAAA | 23072 |
rs11764385 | snp | C/T | | | upstream-variant-2KB, intron-variant | HECW1, LOC105375254 | GRCh38.p7 | 7:43112290 | AAGCGAGGAAAGTGT[C/T]TAAGACAGAGGCCAA | 23072 |
rs11764657 | snp | A/G | 0.471292 | 0.116318 | intron-variant | HECW1 | GRCh38.p7 | 7:43255397 | TAAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 23072 |
rs11764763 | snp | A/C | 0.491987 | 0.0627894 | intron-variant | HECW1 | GRCh38.p7 | 7:43255751 | CAGCTTATTAACAGG[A/C]CTCCAGTTTAGTGAA | 23072 |
rs11765609 | snp | A/T | 0.499234 | 0.0195537 | intron-variant | HECW1 | GRCh38.p7 | 7:43341014 | gtcctttgcagggac[A/T]tggatgaagctggaa | 23072 |
rs11765866 | snp | C/T | 0.380529 | 0.213219 | intron-variant | HECW1 | GRCh38.p7 | 7:43306051 | aggtgtgagccaccc[C/T]gcccagcctaatttt | 23072 |
rs11765875 | snp | A/G | 0.322721 | 0.23919 | intron-variant | HECW1 | GRCh38.p7 | 7:43433218 | AATGCTTTACAGATC[A/G]TTGGACTAAATATTT | 23072 |
rs11766033 | snp | A/C | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43184638 | tctggggagcagaga[A/C]gggctaaaggttgag | 23072 |
rs11766054 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43184553 | ggacgtccctagata[A/G]cttcaggataggggc | 23072 |
rs11766064 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43184728 | gctgtaaagaaatat[C/T]tgagactgggtaatt | 23072 |
rs11766139 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43215059 | CTCTCCTTGGGTTTG[C/T]TTTGTTCTTTTTATC | 23072 |
rs11766157 | snp | C/T | 0.215144 | 0.247558 | intron-variant | HECW1 | GRCh38.p7 | 7:43411728 | tatttttctttattt[C/T]tggtagtgctccttg | 23072 |
rs11766883 | snp | A/T | 0.156319 | 0.231784 | intron-variant | HECW1 | GRCh38.p7 | 7:43212168 | TAAACACAGTTGTGA[A/T]GTTTCCTGAACTATC | 23072 |
rs11767004 | snp | A/G | 0.493658 | 0.0559517 | intron-variant, nc-transcript-variant | HECW1, LOC100506895 | GRCh38.p7 | 7:43509442 | TAGGGTCCCAGTGGA[A/G]GCTTCTTGGAGGTAT | 23072 |
rs11768193 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43392989 | ATGAGAATGAGAGTA[A/G]GAGAGAAAGACATCT | 23072 |
rs11768198 | snp | A/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43393058 | TCTCAATACCCTGCA[A/G]AATCTTCTACACCCC | 23072 |
rs11768401 | snp | G/T | 0.147656 | 0.228091 | intron-variant | HECW1 | GRCh38.p7 | 7:43558623 | ACAATGCACAAAACA[G/T]CTCCCACAACAAAGA | 23072 |
rs11769030 | snp | A/G | 0.142947 | 0.22592 | intron-variant | HECW1 | GRCh38.p7 | 7:43541710 | ATCATTGAATGAACT[A/G]AAATGACTGAATAAT | 23072 |
rs11769055 | snp | A/G | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43187779 | TTCTGATAATTATCC[A/G]ATTCTTTTGGTAATT | 23072 |
rs11769244 | snp | C/T | | | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43269217 | ACACCTTGCCATCTC[C/T]TACAACAAGCATGCT | 23072 |
rs11769310 | snp | C/T | 0.333722 | 0.235565 | intron-variant | HECW1 | GRCh38.p7 | 7:43189359 | ATTTCTAATTAGCTC[C/T]CAGGCGATAGGGACA | 23072 |
rs11769457 | snp | A/G | 0.461592 | 0.133149 | intron-variant | HECW1 | GRCh38.p7 | 7:43259019 | TTAGCCCCCAGATAT[A/G]GGAAAAAGTCAGCAC | 23072 |
rs11769680 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494641 | gacaagtaactggga[C/T]tacaggcatgtgcca | 23072 |
rs11769681 | snp | C/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43494644 | aagtaactgggacta[C/T]aggcatgtgccacca | 23072 |
rs11769714 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43184775 | ttagttggctcatgg[C/T]tctgcaggctgttca | 23072 |
rs11770151 | snp | A/C | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43330232 | tccacttcctccctc[A/C]tgggacactcactct | 23072 |
rs11770215 | snp | C/G | 0.46137 | 0.133501 | intron-variant | HECW1 | GRCh38.p7 | 7:43259345 | tgagctgagatcgca[C/G]tgctgcgctccagcc | 23072 |
rs11770773 | snp | A/G | 0.223225 | 0.248562 | intron-variant | HECW1 | GRCh38.p7 | 7:43549108 | GCCGGACAAAGGAAC[A/G]CACAGCCCATCCCTT | 23072 |
rs11770778 | snp | A/G | 0.286303 | 0.24735 | intron-variant | HECW1 | GRCh38.p7 | 7:43549141 | AGGAGGCCTCCTGAC[A/G]GTGCCATACACTTCT | 23072 |
rs11771096 | snp | A/T | 0.322483 | 0.239262 | intron-variant | HECW1 | GRCh38.p7 | 7:43544070 | AATGTAAAAATTTTT[A/T]AAAAAGGAAAAAAGA | 23072 |
rs11771586 | snp | A/G | 0.306679 | 0.24349 | intron-variant | HECW1 | GRCh38.p7 | 7:43188337 | TGTAGGAGCTAAATA[A/G]CTGCTCCTATGATTG | 23072 |
rs11771692 | snp | A/G | 0.459347 | 0.136653 | intron-variant, upstream-variant-2KB | HECW1 | GRCh38.p7 | 7:43248885 | TGCATGTGAGGCCAC[A/G]ACCTCTAGACCCCAG | 23072 |
rs11771902 | snp | C/T | 0.352721 | 0.227922 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125552 | acaaggtcaggagtt[C/T]gagaccagcctggcc | 23072 |
rs11772689 | snp | A/G | 0.18134 | 0.240387 | intron-variant | HECW1 | GRCh38.p7 | 7:43344906 | TTTGCTAGTAGTTTC[A/G]ATCTTGTCTTCTTTT | 23072 |
rs11772780 | snp | C/T | 0.333491 | 0.235646 | intron-variant | HECW1 | GRCh38.p7 | 7:43188067 | TCCTGATGACAGGAG[C/T]GGCTTACCTTGTGAG | 23072 |
rs11772786 | snp | C/G | 0.214541 | 0.247473 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156356 | TGTGCCCAAGCCAGT[C/G]TTTCTTCTCTCACTT | 23072 |
rs11773602 | snp | C/G | 0.221141 | 0.248329 | intron-variant | HECW1 | GRCh38.p7 | 7:43433609 | CTTGCTCATAGTGGC[C/G]CCAGCGGTGGGCCTT | 23072 |
rs11773859 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | HECW1 | GRCh38.p7 | 7:43259346 | gagctgagatcgcag[C/T]gctgcgctccagcct | 23072 |
rs11970848 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | HECW1 | GRCh38.p7 | 7:43185913 | actttctgaaaattt[A/G]acaatcttctctcac | 23072 |
rs11971252 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | HECW1 | GRCh38.p7 | 7:43555892 | ACTAAAAAGGCAGAA[C/T]TTGCATTTGTTAAGT | 23072 |
rs11971407 | snp | A/G | 0.324619 | 0.238604 | intron-variant | HECW1 | GRCh38.p7 | 7:43475163 | ACAACAACAAAAAAG[A/G]AAAAGGGCCCCAAAA | 23072 |
rs11971577 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | HECW1 | GRCh38.p7 | 7:43465083 | ctaggattacaggca[C/G]gagacatcacacctg | 23072 |
rs11971631 | snp | C/T | 0.499104 | 0.0211472 | intron-variant | HECW1 | GRCh38.p7 | 7:43340046 | AGGAAAAAGGGGGTA[C/T]AGGTTACCAGAAACC | 23072 |
rs11971844 | snp | A/G | 0.116838 | 0.211584 | intron-variant | HECW1 | GRCh38.p7 | 7:43247089 | GAGAAGCACAGCTCC[A/G]TGTCTGCTATACTCT | 23072 |
rs11971859 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | HECW1 | GRCh38.p7 | 7:43304792 | agccatagcacccag[A/C]cTCAACAAAGTATTT | 23072 |
rs11972242 | snp | C/T | 0.492337 | 0.0614248 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43140034 | AATAAAGGTTATTTG[C/T]AATGTGAATATTATT | 23072 |
rs11972767 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | HECW1 | GRCh38.p7 | 7:43275299 | ctctcataacataat[A/G]ttacataagtaaatc | 23072 |
rs11973439 | snp | G/T | 0.449979 | 0.150028 | intron-variant | HECW1 | GRCh38.p7 | 7:43332452 | GCTCTAAAGGCCTGT[G/T]GCAGGTGTGTGTGGC | 23072 |
rs11974508 | snp | C/T | 0.179105 | 0.239737 | intron-variant | HECW1 | GRCh38.p7 | 7:43238671 | GAAAAAATGTATGAA[C/T]GAATGAAAATGAAAA | 23072 |
rs11974924 | snp | C/T | 0.147656 | 0.228091 | intron-variant | HECW1 | GRCh38.p7 | 7:43237382 | TTCAGCTCATCTGTT[C/T]GGTGTGTCTCCCCTC | 23072 |
rs11974938 | snp | C/T | 0.440884 | 0.161442 | intron-variant | HECW1 | GRCh38.p7 | 7:43419084 | TAAACTTGGGCTGAG[C/T]TTCTATACATCGTTT | 23072 |
rs11975113 | snp | A/C | | | intron-variant | HECW1 | GRCh38.p7 | 7:43318517 | CAGAGAAGGGGCAGC[A/C]TAAAATGTGCAATCC | 23072 |
rs11975352 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | HECW1 | GRCh38.p7 | 7:43431299 | CAGGCCTCTATTTCC[A/G]TCATTCTGTTCCTTC | 23072 |
rs11975714 | snp | C/T | 0.312104 | 0.242163 | intron-variant | HECW1 | GRCh38.p7 | 7:43264656 | caagaccatcctggc[C/T]aacacagtgaacccc | 23072 |
rs11975734 | snp | C/T | 0.136847 | 0.222927 | intron-variant | HECW1 | GRCh38.p7 | 7:43264720 | gtggtggcgggcacc[C/T]gtagtctcagttact | 23072 |
rs11975750 | snp | C/T | 0.267091 | 0.249415 | intron-variant | HECW1 | GRCh38.p7 | 7:43475322 | AAATTTAAGCACAAT[C/T]GTAAGAACAAAATCT | 23072 |
rs11975950 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | HECW1 | GRCh38.p7 | 7:43420043 | agaaaggtaaaaaca[A/C]cttcaaataaggaag | 23072 |
rs11976276 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HECW1 | GRCh38.p7 | 7:43289852 | gttaggcaggaaaag[G/T]caggacatcttgaag | 23072 |
rs11976327 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HECW1 | GRCh38.p7 | 7:43256622 | ctcaaaaaaaaaaaa[A/G]aaaagaaaagaaaaG | 23072 |
rs11976874 | snp | A/C | 0.0825414 | 0.185628 | intron-variant, upstream-variant-2KB | HECW1, LOC102724903 | GRCh38.p7 | 7:43303233 | TTGAGCAAAGCAGTG[A/C]ATGGTCCAATCATGC | 23072 |
rs11978372 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HECW1 | GRCh38.p7 | 7:43465173 | ACTAGAAACATGAGG[A/G]AAAAGCAGCAGAAAG | 23072 |
rs11978433 | snp | A/G | 0.102014 | 0.201495 | intron-variant | HECW1 | GRCh38.p7 | 7:43287021 | ATGGTTGGGGGTAGC[A/G]GGGAGTTGTTTAAGG | 23072 |
rs11978634 | snp | C/T | 0.274393 | 0.248807 | intron-variant | HECW1 | GRCh38.p7 | 7:43246990 | GAGCACCCCTCCATA[C/T]ATAGGTGGAGTGGAA | 23072 |
rs11978689 | snp | C/G | 0.275197 | 0.248727 | intron-variant | HECW1 | GRCh38.p7 | 7:43247058 | TGACAACTAGGCAAT[C/G]AATCTGTTCTTAAAA | 23072 |
rs11979234 | snp | A/G | 0.102726 | 0.202016 | intron-variant | HECW1 | GRCh38.p7 | 7:43287383 | agggttgtgatgggc[A/G]ggcaggaggaagagc | 23072 |
rs11979877 | snp | A/G | 0.373799 | 0.217195 | intron-variant | HECW1 | GRCh38.p7 | 7:43265860 | caatgatctgctaga[A/G]tgacttataaaacac | 23072 |
rs11979901 | snp | A/G | 0.380034 | 0.213521 | intron-variant | HECW1 | GRCh38.p7 | 7:43265950 | tgaagaggaaacttg[A/G]gggggggtgtggatt | 23072 |
rs11979957 | snp | A/G | 0.143622 | 0.226238 | intron-variant | HECW1 | GRCh38.p7 | 7:43441841 | AAATGTAAAAAGCTC[A/G]CAACCACACAAAAAC | 23072 |
rs11980717 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | HECW1 | GRCh38.p7 | 7:43455097 | CCTGTATTATGTAGT[C/G]AATCATCCATGCTTC | 23072 |
rs11980937 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HECW1 | GRCh38.p7 | 7:43470299 | TCAGAGCTCGGTTTC[A/G]GGTAGCCACGTTTAC | 23072 |
rs11981087 | snp | C/G | 0.338976 | 0.23363 | intron-variant | HECW1 | GRCh38.p7 | 7:43561096 | ACCCACTGCTGGAGA[C/G]CCACATGAGTCTTCC | 23072 |
rs11982126 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | HECW1 | GRCh38.p7 | 7:43556343 | GGTAAGATGCCCGGA[A/G]CAACATCACAGGGGA | 23072 |
rs11982177 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | HECW1 | GRCh38.p7 | 7:43431381 | TCACTCCTCCCACAT[A/G]CCCTCAATCTTGGGA | 23072 |
rs11982278 | snp | A/T | 0.274929 | 0.248754 | intron-variant | HECW1 | GRCh38.p7 | 7:43247010 | GTGGAGTGGAAGGAG[A/T]TGGTGGCTGGAAGCT | 23072 |
rs11982304 | snp | C/T | 0.275197 | 0.248727 | intron-variant | HECW1 | GRCh38.p7 | 7:43247092 | AAGCACAGCTCCATG[C/T]CTGCTATACTCTCCA | 23072 |
rs11982538 | snp | G/T | 0.306679 | 0.24349 | intron-variant | HECW1 | GRCh38.p7 | 7:43271430 | gaactctttcttccc[G/T]aattatatgattctg | 23072 |
rs11982866 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43347839 | ttgacttgcatatgt[C/T]aaaccatccctacat | 23072 |
rs11982908 | snp | A/G | 0.499853 | 0.008585 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43144159 | TTTTGAAGAATGTTC[A/G]TCAGGTATTTTATAG | 23072 |
rs11983836 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HECW1 | GRCh38.p7 | 7:43232670 | gtgaaactcatgata[C/T]ctcttaaaacttctt | 23072 |
rs11983947 | snp | A/C/G | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43385969 | tctgtggaaaagcct[A/C/G]ctttcaagctcattc | 23072 |
rs11984170 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | HECW1 | GRCh38.p7 | 7:43394441 | caatcactgagacaa[C/T]gagtattgccaggaa | 23072 |
rs11984240 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HECW1 | GRCh38.p7 | 7:43308782 | acctgccaacacgcc[C/T]ggctaatttttgtac | 23072 |
rs11984436 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | HECW1 | GRCh38.p7 | 7:43178337 | ACTATCCCCATGGAC[C/T]GAGCCACAAGCTTTC | 23072 |
rs12056162 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43193303 | tgacctgtatcttga[A/G]aaaccagtcctgccg | 23072 |
rs12112309 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HECW1 | GRCh38.p7 | 7:43283016 | ccagctactcgggag[A/G]ctgaggcaggagaat | 23072 |
rs12112386 | snp | A/T | 0.489024 | 0.0732638 | intron-variant | HECW1 | GRCh38.p7 | 7:43170612 | GTGGCTGGAAAATAG[A/T]GGTAGCAGGGGTTGC | 23072 |
rs12154569 | snp | C/G | 0.0991586 | 0.199366 | intron-variant | HECW1 | GRCh38.p7 | 7:43313251 | CCAAAAGTTAAAATT[C/G]AATTTATTTCTGAAA | 23072 |
rs12154658 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | HECW1 | GRCh38.p7 | 7:43313637 | ccactgccctcggcc[A/G]catattttgtttcat | 23072 |
rs12155068 | snp | C/G | 0.322721 | 0.23919 | intron-variant | HECW1 | GRCh38.p7 | 7:43394006 | TTATTCTTAGAAAGA[C/G]ACAAATTTGGGGTGG | 23072 |
rs12155375 | snp | A/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43385056 | AAGGACAATAATTAC[A/T]AGGAGTTTCATAATT | 23072 |
rs12155422 | snp | C/T | | | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43156831 | Cattcaccacattat[C/T]ttcccacaccaaagt | 23072 |
rs12375030 | snp | C/G | 0.178465 | 0.239547 | intron-variant | HECW1, LOC102724903 | GRCh38.p7 | 7:43298324 | CAGGGCAGAGGCCAT[C/G]ATTTCTATTTCAGTT | 23072 |
rs12530642 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43263337 | CAAGCCATGGAATTG[C/G]TAAAATAATCTGAGC | 23072 |
rs12530660 | snp | A/G | 0.298651 | 0.24522 | intron-variant | HECW1 | GRCh38.p7 | 7:43239116 | AACGTGAGACCAGAC[A/G]GCCACGTTTTTGGCC | 23072 |
rs12530692 | snp | A/G | 0.361684 | 0.223667 | intron-variant | HECW1 | GRCh38.p7 | 7:43239249 | ACAAAGAATAGTTTT[A/G]TTAAATTAGCAAATG | 23072 |
rs12531047 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | HECW1 | GRCh38.p7 | 7:43380275 | tgctttgttgcccac[A/G]ctggtctcaaactcc | 23072 |
rs12531643 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43174878 | CCTAACAGCAACTCA[C/G]ATGGAATATACTTAC | 23072 |
rs12532706 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | HECW1 | GRCh38.p7 | 7:43370086 | ttacagactggaaga[A/C]tatatctgcaaaata | 23072 |
rs12532855 | snp | C/T | 0.184838 | 0.241358 | intron-variant | HECW1 | GRCh38.p7 | 7:43306972 | AAACAACAAAGAGCA[C/T]ATCACTTAATTCAAA | 23072 |
rs12532864 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HECW1 | GRCh38.p7 | 7:43307003 | ACATTTCAACAATTA[C/T]GATGTCATTTAAGTT | 23072 |
rs12532870 | snp | A/C | 0.197703 | 0.244469 | intron-variant | HECW1 | GRCh38.p7 | 7:43307079 | AAATAGGAAAAAAAA[A/C]CAAAAACAAAAAAAC | 23072 |
rs12533232 | snp | A/C | 0.270621 | 0.249148 | intron-variant | HECW1 | GRCh38.p7 | 7:43471214 | CCCATTGATAAGGGG[A/C]ATAGATTGAGAAAAG | 23072 |
rs12533506 | snp | A/G | 0.188316 | 0.242271 | intron-variant | HECW1 | GRCh38.p7 | 7:43307543 | ATCACTGTCTAGGAA[A/G]ACAGTGGCCTTTTAT | 23072 |
rs12533636 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | HECW1 | GRCh38.p7 | 7:43368208 | CAGACAAGAAAACAG[A/G]CAATGACAGAGCACT | 23072 |
rs12534105 | snp | A/G | 0.499767 | 0.0107802 | intron-variant | HECW1 | GRCh38.p7 | 7:43218873 | TTTTAAGGAGCAGAG[A/G]GTTTAATAGACAAGA | 23072 |
rs12534113 | snp | C/G | 0.499839 | 0.00898417 | intron-variant | HECW1 | GRCh38.p7 | 7:43219054 | GATTGGTTTGACCAG[C/G]CATGTCATTCATGTA | 23072 |
rs12534681 | snp | A/G | 0.320096 | 0.239972 | intron-variant | HECW1 | GRCh38.p7 | 7:43462512 | AAAAAAAGAGAAAAG[A/G]AAAAAGAAATGCACA | 23072 |
rs12534814 | snp | C/T | 0.293037 | 0.246268 | intron-variant | HECW1 | GRCh38.p7 | 7:43541757 | TTCAAAAGTATCCAA[C/T]TGTTAGGATAAGTCT | 23072 |
rs12534962 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | HECW1 | GRCh38.p7 | 7:43450298 | TTACTTTCTTGGCTC[A/G]CCAGCTCCTTGACCT | 23072 |
rs12535883 | snp | A/G | 0.177824 | 0.239355 | intron-variant | HECW1 | GRCh38.p7 | 7:43474310 | aaaaattagctgggc[A/G]tggtggcgggtgcct | 23072 |
rs12536033 | snp | C/G | 0.294064 | 0.246086 | intron-variant | HECW1 | GRCh38.p7 | 7:43447213 | ACACTTTTCTTAGCT[C/G]AGAGCCATACAACCC | 23072 |
rs12536567 | snp | C/T | 0.497933 | 0.032082 | intron-variant, upstream-variant-2KB | HECW1, LOC105375254 | GRCh38.p7 | 7:43113042 | CAGCGCCCTCCCTTC[C/T]CGGGGCCGAGATCCA | 23072 |
rs12537018 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | HECW1 | GRCh38.p7 | 7:43368563 | AGGGAAGGGATTCGG[C/T]ATCCTCTCTCTAGAT | 23072 |
rs12537565 | snp | A/C | 0.105569 | 0.204058 | intron-variant | HECW1 | GRCh38.p7 | 7:43253306 | GAGTCCTGCCACATG[A/C]CTACACATAGTTGTT | 23072 |
rs12537779 | snp | A/T | 0.323908 | 0.238825 | intron-variant | HECW1 | GRCh38.p7 | 7:43215082 | TTTTTATCCTGATTT[A/T]AAAAAATGTAAGGAT | 23072 |
rs12538451 | snp | C/G | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43495541 | CAAGGCCTTTCTCTT[C/G]CTTGTCTTTGTGCCC | 23072 |
rs12539311 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HECW1 | GRCh38.p7 | 7:43527145 | TAAATTCCCTTCTTG[C/T]GTGAAATTAAATATA | 23072 |
rs12540272 | snp | A/G | 0.325327 | 0.238382 | intron-variant | HECW1 | GRCh38.p7 | 7:43215107 | AAGGATTGAATTTTC[A/G]GGTTCTTGATTTACA | 23072 |
rs12540532 | snp | C/T | 0.105924 | 0.204309 | intron-variant | HECW1 | GRCh38.p7 | 7:43263085 | CTTATCTGCATTTTC[C/T]GCAATTACTTACCTG | 23072 |
rs12540611 | snp | A/C | 0.0865458 | 0.189163 | intron-variant | HECW1 | GRCh38.p7 | 7:43345424 | TGGttttttattttt[A/C]tttttattattttat | 23072 |
rs12540702 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | HECW1 | GRCh38.p7 | 7:43285653 | CATCTTTATTAAAAA[A/T]TTTTTAAAAATAGCT | 23072 |
rs12666190 | snp | C/T | 0 | 0 | intron-variant | HECW1 | GRCh38.p7 | 7:43440137 | CAGTGGCCATGCAGC[C/T]TGAGCCATGGCAGAA | 23072 |
rs12666458 | snp | A/G | 0.439085 | 0.163545 | intron-variant | HECW1 | GRCh38.p7 | 7:43422333 | GAACTTTTAGAGTAT[A/G]CTTCTCTTTTTTTAA | 23072 |
rs12666476 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | HECW1 | GRCh38.p7 | 7:43271117 | TGTGTTGTATGTATA[C/T]ATATTTCATTCTAAA | 23072 |
rs12666597 | snp | A/G | 0.406123 | 0.195258 | intron-variant | HECW1 | GRCh38.p7 | 7:43334947 | TTCATATTTACCCTC[A/G]AAAAGAAGAGGCTTA | 23072 |
rs12666661 | snp | C/T | 0.497829 | 0.0328757 | intron-variant | HECW1 | GRCh38.p7 | 7:43556314 | TCAGGAAGGTGCAGC[C/T]GGCCAGTGCAGAGGG | 23072 |
rs12666862 | snp | C/T | 0.413582 | 0.189052 | intron-variant | HECW1, HECW1-IT1 | GRCh38.p7 | 7:43125477 | AGAGTGAGGCATTgg[C/T]cgggtgtggtggctc | 23072 |
rs12667397 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43324040 | actctatctcaaaaa[A/G]gaaaaaaaaaGGCTT | 23072 |
rs12667830 | snp | G/T | | | intron-variant | HECW1 | GRCh38.p7 | 7:43378475 | AAAGATTCTGCATTG[G/T]CCTGTCAGACATCCC | 23072 |
rs12668163 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant | HECW1 | GRCh38.p7 | 7:43467591 | CTCTGGCAGAGTGTC[A/G/T]GGGAGAGACTGAGCT | 23072 |
rs12669012 | snp | A/C | 0.18989 | 0.242666 | intron-variant | HECW1 | GRCh38.p7 | 7:43189201 | AAAGAAAGAACAAAT[A/C]TCTTTTAAAATTGCT | 23072 |
rs12669317 | snp | A/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43349869 | agtatcgaaatatga[A/G]gtaccattgctttca | 23072 |
rs12670602 | snp | A/C | 0.464735 | 0.128019 | intron-variant | HECW1 | GRCh38.p7 | 7:43316424 | GGCCCAGATTCTAAG[A/C]AGAAATAGCTGCTTA | 23072 |
rs12670903 | snp | A/G | 0.427119 | 0.176434 | intron-variant | HECW1 | GRCh38.p7 | 7:43335114 | GAGTAGATTATGTCA[A/G]TTCTTTTTAAACAGT | 23072 |
rs12671210 | snp | A/G | 0.172028 | 0.23753 | intron-variant | HECW1 | GRCh38.p7 | 7:43293081 | TAGAATTAGCCGGGC[A/G]TGGTGGAAGGCGCCT | 23072 |
rs12671845 | snp | A/C | 0.264632 | 0.249571 | intron-variant, upstream-variant-2KB | HECW1, LOC100506895 | GRCh38.p7 | 7:43524295 | GAAATCTACCCCAGG[A/C]AGACACAACAGGTTT | 23072 |
rs12672368 | snp | C/G | | | intron-variant | HECW1 | GRCh38.p7 | 7:43229864 | gttgccatcatcagt[C/G]cagcttgtattgggt | 23072 |
rs12673696 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HECW1 | GRCh38.p7 | 7:43372747 | TCTCTCTTCTCATGA[C/G]TGGTCTGGCTTTATC | 23072 |