SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs182594 | snp | C/G | 0.495596 | 0.0467178 | intron-variant | PHF14 | GRCh38.p7 | 7:11005495 | GACAAAACAGAGAAA[C/G]AGTGAGAGAAAGAGA | 9678 |
rs190074 | snp | A/G | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974321 | GGATACACTTACTAA[A/G]GAATCCGTGAGGTGG | 9678 |
rs190075 | snp | G/T | 0.453453 | 0.145282 | | | GRCh38.p7 | 7:10969845 | TGGAGATCCGAATTT[G/T]GGTCTAGGCTTGGCC | 9678 |
rs191984 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11075701 | Ttgatatagtttgga[A/T]atatgtctcctccaa | 9678 |
rs218962 | snp | C/T | 0.455144 | 0.142885 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966431 | ttctttgatgccttt[C/T]ggccaatcagatggt | 9678 |
rs218963 | snp | A/G | 0.46865 | 0.121211 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964631 | gatcttccccaacct[A/G]gcaagacaggccaac | 9678 |
rs218964 | snp | C/T | 0.476401 | 0.106032 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963566 | acatctacagaactc[C/T]ccaccccaaatcaac | 9678 |
rs218965 | snp | C/T | 0.446602 | 0.154427 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982937 | TCCCTCTTTCTGAGA[C/T]GCAGATCTCCCTTTT | 9678 |
rs218966 | snp | C/T | 0.452541 | 0.146551 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982603 | TCCTTCTCTTTCTCC[C/T]TTTTCTTTCTAGGTC | 9678 |
rs218973 | snp | A/G | 0.4444 | 0.15719 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960237 | ggggtggggtgctgg[A/G]gaagggatagtgttg | 9678 |
rs218974 | snp | A/G | 0.446771 | 0.154211 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959665 | tccagctacagcctc[A/G]cagagagccggtgcc | 9678 |
rs218975 | snp | A/G | 0.435837 | 0.167226 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959557 | ctcactcactcacat[A/G]cctctcaccactctg | 9678 |
rs218976 | snp | C/G | 0.468047 | 0.122292 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956775 | ATCTTCCAGTTCCTA[C/G]TGGCTTCTGGTGTTC | 9678 |
rs218980 | snp | C/G | 0.409041 | 0.192888 | | | GRCh38.p7 | 7:10971592 | acaatattgcattta[C/G]gttattaATCTTTTG | 9678 |
rs218981 | snp | C/T | 0.405776 | 0.195535 | | | GRCh38.p7 | 7:10970547 | ATTGCTTTGTTGCCC[C/T]GGCTGGAGTGTGTAG | 9678 |
rs218982 | snp | A/G | 0.456332 | 0.141164 | | | GRCh38.p7 | 7:10970108 | TTTCCAAAAAACAGC[A/G]AGCACAAACTGCCTC | 9678 |
rs218983 | snp | C/T | 0.427879 | 0.175668 | | | GRCh38.p7 | 7:10969465 | AAAGAGATGAAGTGC[C/T]TAGGGAAAGTAAAAT | 9678 |
rs220089 | snp | C/T | 0.491157 | 0.065903 | intron-variant | PHF14 | GRCh38.p7 | 7:11007460 | TTAGATAAAAATTCA[C/T]TTTGAAACTTAAAAA | 9678 |
rs220090 | snp | A/G | 0.444533 | 0.157025 | intron-variant | PHF14 | GRCh38.p7 | 7:11006683 | CAGATATCCTCGGAA[A/G]AGCTCCCCCAGGAGA | 9678 |
rs220091 | snp | C/T | 0.496105 | 0.0439572 | intron-variant | PHF14 | GRCh38.p7 | 7:11005425 | CTCTCACTGGTCAAA[C/T]TTGGACAATGTAATA | 9678 |
rs220092 | snp | A/G | 0.434831 | 0.168337 | intron-variant | PHF14 | GRCh38.p7 | 7:11004091 | CTGGCTGATTTTTCT[A/G]TATTTTGTAGAGACA | 9678 |
rs220093 | snp | G/T | 0.438806 | 0.163867 | intron-variant | PHF14 | GRCh38.p7 | 7:11027126 | TCACTCTGAAATCCC[G/T]TGCTCAATTTCAACA | 9678 |
rs220094 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | PHF14 | GRCh38.p7 | 7:11027234 | TCTCTTTATCTCTCT[C/T]GCTCAATCTCATGTT | 9678 |
rs220095 | snp | A/T | 0.496105 | 0.0439572 | intron-variant | PHF14 | GRCh38.p7 | 7:11017344 | gttgcatgaaatgta[A/T]attagtacaaccatg | 9678 |
rs220096 | snp | C/T | 0.445724 | 0.155538 | intron-variant | PHF14 | GRCh38.p7 | 7:11013097 | GTTGGCAAACACTTA[C/T]TGAGGTCCCTTTGTA | 9678 |
rs220097 | snp | A/G | 0.497211 | 0.037236 | intron-variant | PHF14 | GRCh38.p7 | 7:11009896 | TTTAAACCTCCTACA[A/G]TTAATCTTAGGAATG | 9678 |
rs220098 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065172 | GTAGATGGCAAAAAA[A/C]CAGCACTTAAAAAAA | 9678 |
rs220099 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064837 | TGTGATCATGTACAA[C/T]GGGGGGAAAACCAAG | 9678 |
rs220100 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | PHF14 | GRCh38.p7 | 7:11078627 | TCAGGTGTAAGGAAT[C/G]TGAGTCATTTATAGA | 9678 |
rs721028 | snp | A/G | 0.167158 | 0.235875 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065358 | TTGGAAGTAGTTATG[A/G]AACTACTTAGTGATA | 9678 |
rs766817 | snp | C/G | 0 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958691 | taaaataaaaCTACA[C/G]AAGTAAGCAGTTGGC | 9678 |
rs1026903 | snp | C/T | 0.174288 | 0.23826 | intron-variant | PHF14 | GRCh38.p7 | 7:11022248 | TTACCATACAATCTA[C/T]ATACTAAAATTTATA | 9678 |
rs1029583 | snp | C/G | 0.492137 | 0.0622048 | intron-variant | PHF14 | GRCh38.p7 | 7:11134941 | TCAGCATGTTTATGT[C/G]CAAGTATTCATATTA | 9678 |
rs1029584 | snp | G/T | 0.492727 | 0.0598633 | intron-variant | PHF14 | GRCh38.p7 | 7:11109711 | TTGTTCTGGCATTAA[G/T]AAAGAATAATAAATA | 9678 |
rs1057436 | snp | C/G | 0.487809 | 0.0771174 | intron-variant | PHF14 | GRCh38.p7 | 7:11126591 | AAATCCCTAACTTTT[C/G]TCTTCCTGTCTACTC | 9678 |
rs1057437 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11126619 | CTCCTTCCTTTCTCC[C/T]TCACATTTCCAAGCA | 9678 |
rs1154920 | snp | C/T | 0.406986 | 0.194565 | intron-variant | PHF14 | GRCh38.p7 | 7:10978615 | ACAAAATGCCAATAG[C/T]GCCAAGGTTGAGAAA | 9678 |
rs1154921 | snp | A/G | 0.45946 | 0.136478 | intron-variant | PHF14 | GRCh38.p7 | 7:10978597 | CAAGGTTGAGAAACC[A/G]TTAACTCGTATATAC | 9678 |
rs1154922 | snp | C/T | 0.409382 | 0.192607 | intron-variant | PHF14 | GRCh38.p7 | 7:10978420 | GTTCATAGTTCCACT[C/T]TTACCTCCTCTCCTC | 9678 |
rs1154923 | snp | G/T | 0.171704 | 0.237423 | intron-variant | PHF14 | GRCh38.p7 | 7:10978365 | AATCTCATTTCCTAT[G/T]AAAGACTTGAACTAC | 9678 |
rs1483201 | snp | C/T | 0.499424 | 0.0169631 | intron-variant | PHF14 | GRCh38.p7 | 7:11058143 | GGTCCTTTTCTGATA[C/T]ATTTTGAGGCTGAAA | 9678 |
rs1483202 | snp | C/T | 0.495855 | 0.045338 | intron-variant | PHF14 | GRCh38.p7 | 7:11058025 | AACACAGATACGTTA[C/T]CTGGAAATTCCACAT | 9678 |
rs1483203 | snp | C/T | 0.44333 | 0.158505 | intron-variant | PHF14 | GRCh38.p7 | 7:11057956 | TTTGACAGTAATTAG[C/T]TAACCTATTAAAAGT | 9678 |
rs1483204 | snp | A/C | 0.499295 | 0.0187567 | intron-variant | PHF14 | GRCh38.p7 | 7:11057666 | TTTATTCAGGCCGGG[A/C]ACAGTGGCTCAGGCC | 9678 |
rs1483205 | snp | A/T | 0.437542 | 0.165312 | intron-variant | PHF14 | GRCh38.p7 | 7:11051295 | TGCTGGGATTATGGG[A/T]GTGAGCCACTGCAGC | 9678 |
rs1531834 | snp | A/T | 0.44858 | 0.151875 | intron-variant | PHF14 | GRCh38.p7 | 7:11044327 | CTTTTCTTTTTTTTT[A/T]AATTTCAACTTTTAT | 9678 |
rs1547944 | snp | C/G | 0.499982 | 0.00299515 | intron-variant | PHF14 | GRCh38.p7 | 7:11119430 | TAATATATTCCACAC[C/G]ACTTCTGAATTTTAT | 9678 |
rs1547945 | snp | A/T | 0.491473 | 0.0647364 | intron-variant | PHF14 | GRCh38.p7 | 7:11119374 | TTGATTATATAACCT[A/T]ATTTTAATATTTCAA | 9678 |
rs1625381 | snp | A/G | 0.44651 | 0.154543 | intron-variant | PHF14 | GRCh38.p7 | 7:11026109 | ttttttttttttttt[A/G]atggagtctcacact | 9678 |
rs1629587 | snp | A/G | 0.435263 | 0.167862 | intron-variant | PHF14 | GRCh38.p7 | 7:11025651 | cctgctaccatgccc[A/G]gctaattttttgtat | 9678 |
rs1636753 | snp | C/T | 0.449853 | 0.150196 | intron-variant | PHF14 | GRCh38.p7 | 7:11021324 | TTTATAACTTTGTAA[C/T]TAAGACAAATCTACA | 9678 |
rs1636754 | snp | A/G | 0.438806 | 0.163867 | intron-variant | PHF14 | GRCh38.p7 | 7:11019075 | taggatttatccctg[A/G]gttgcaagcatggtt | 9678 |
rs1636755 | snp | C/T | 0.438386 | 0.164349 | intron-variant | PHF14 | GRCh38.p7 | 7:11019031 | tcaatcaacatgata[C/T]atcacatcaacagga | 9678 |
rs1636756 | snp | C/T | 0.492871 | 0.0592773 | intron-variant | PHF14 | GRCh38.p7 | 7:11018379 | aaaaatattccatgt[C/T]cacaaactggaagaa | 9678 |
rs1636757 | snp | A/T | 0.449218 | 0.151037 | intron-variant | PHF14 | GRCh38.p7 | 7:11018083 | agaactcagaaacaa[A/T]tccacgcacctaagt | 9678 |
rs1640699 | snp | C/G | 0.499663 | 0.0129749 | intron-variant | PHF14 | GRCh38.p7 | 7:10977986 | GTCTGGTTAATAGAA[C/G]TAATACATGTCTGCA | 9678 |
rs1640700 | snp | A/C | 0.475081 | 0.108804 | intron-variant | PHF14 | GRCh38.p7 | 7:10977651 | TCAATCAAAAATGAG[A/C]AGCTTACTTTTGCTT | 9678 |
rs1640701 | snp | C/G | 0.459914 | 0.13578 | intron-variant | PHF14 | GRCh38.p7 | 7:10977063 | TAATCTAGAGTAAGC[C/G]AATATCTCAGCTATG | 9678 |
rs1640702 | snp | A/G | 0.457154 | 0.139954 | intron-variant | PHF14 | GRCh38.p7 | 7:10976987 | TTTCTGTTGACTACT[A/G]ATCATTTTAAATACA | 9678 |
rs1640703 | snp | A/G | 0.448708 | 0.151707 | intron-variant | PHF14 | GRCh38.p7 | 7:10976893 | CTGAGACCACAGATC[A/G]CAAATTTAAGCTCCC | 9678 |
rs1640704 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | PHF14 | GRCh38.p7 | 7:10992004 | AATTTTTTAAGAATG[C/T]TTTCTATCAGACTAA | 9678 |
rs1640705 | snp | C/T | 0.435119 | 0.16802 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968594 | TCTCTGCCAGGTGAA[C/T]AGGGCTTCTTATTTG | 9678 |
rs1640710 | snp | A/C | 0.40733 | 0.194287 | intron-variant | PHF14 | GRCh38.p7 | 7:10988697 | GTTCAAAAAGAGGAA[A/C]ATGAACTGATAATTT | 9678 |
rs1640712 | snp | A/G | 0.476918 | 0.104919 | intron-variant | PHF14 | GRCh38.p7 | 7:10986011 | actgcaccccagtcc[A/G]ggaaacaaagcgaga | 9678 |
rs1640713 | snp | A/C | 0.45866 | 0.137698 | intron-variant | PHF14 | GRCh38.p7 | 7:10986008 | gcaccccagtccagg[A/C]aacaaagcgagaatc | 9678 |
rs1681281 | snp | A/G | 0.439641 | 0.162899 | intron-variant | PHF14 | GRCh38.p7 | 7:11021696 | AATATAAAGATACAC[A/G]TCTTCAACAAGCAGC | 9678 |
rs1681283 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11068920 | atgcaagattcctaa[A/G]gtcgaaactacatca | 9678 |
rs1681284 | snp | C/T | 0.474723 | 0.109542 | intron-variant | PHF14 | GRCh38.p7 | 7:10989047 | GGGCTGACAAATGGC[C/T]GGCAAATAAAACTGA | 9678 |
rs1681285 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10988434 | GTGGAATTAAAATTA[A/T]TCAGCCCTGGAAAAA | 9678 |
rs1681286 | snp | C/T | 0.462144 | 0.132269 | intron-variant | PHF14 | GRCh38.p7 | 7:10988127 | AAATATTTCCCTAAC[C/T]AAATGGCTAGCAGAC | 9678 |
rs1681290 | snp | A/G | 0.498109 | 0.0306926 | intron-variant | PHF14 | GRCh38.p7 | 7:10991692 | GTTTCTTTAAAGGTC[A/G]GTGTTCTGGTATTGT | 9678 |
rs1681291 | snp | A/G | 0.497803 | 0.033074 | intron-variant | PHF14 | GRCh38.p7 | 7:10991721 | GTATTTTATGGTACT[A/G]tttcttgtttgtttt | 9678 |
rs1681292 | snp | A/G | 0.43978 | 0.162738 | intron-variant | PHF14 | GRCh38.p7 | 7:10991785 | ttttttttggtagag[A/G]cagggttttgctatg | 9678 |
rs1681293 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020605 | gatcacttaagctca[A/G]gagtttgagaccagc | 9678 |
rs1681302 | snp | C/G | 0.41275 | 0.189769 | intron-variant | PHF14 | GRCh38.p7 | 7:10978907 | TTGAAGACAGCCAAT[C/G]AGTCAACACAACTCA | 9678 |
rs1681305 | snp | C/T | 0.404209 | 0.196773 | intron-variant | PHF14 | GRCh38.p7 | 7:10977213 | ATTTAATCTCCTATT[C/T]GTAAGTAGGGCTGGG | 9678 |
rs1681309 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11075366 | atttggcccacggat[C/T]tgccggctgtacaag | 9678 |
rs1681310 | snp | C/T | 0.410399 | 0.191761 | intron-variant | PHF14 | GRCh38.p7 | 7:10986797 | TTCCCATTTTCAAGA[C/T]TTTGAAACTAAAGTT | 9678 |
rs1681311 | snp | C/T | 0.45866 | 0.137698 | intron-variant | PHF14 | GRCh38.p7 | 7:10987188 | GTCCTAAAAAAAGGT[C/T]AGTTCTGTAACATTT | 9678 |
rs1681312 | snp | C/T | 0.410399 | 0.191761 | intron-variant | PHF14 | GRCh38.p7 | 7:10987342 | ATTTTACAGGAAATG[C/T]GCTGGAATTTCCTTG | 9678 |
rs1833011 | snp | C/T | 0.490398 | 0.0686206 | intron-variant | PHF14 | GRCh38.p7 | 7:11091683 | GCAACCTCTGCCTCC[C/T]GGGTTCAGGTGATTC | 9678 |
rs2020391 | snp | C/G | 0.454904 | 0.143228 | intron-variant | PHF14 | GRCh38.p7 | 7:11081712 | cgtgccaccacaccc[C/G]gctaattttttgtat | 9678 |
rs2108111 | snp | C/T | 0.438246 | 0.16451 | intron-variant | PHF14 | GRCh38.p7 | 7:11034042 | GAAGACATAAAAACC[C/T]GGATACAAATCTTGG | 9678 |
rs2108112 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11032742 | ATGGGTGAAGGAGAC[C/T]TAAAAGATGCCAGAA | 9678 |
rs2108114 | snp | C/T | 0.437683 | 0.165152 | intron-variant | PHF14 | GRCh38.p7 | 7:11057398 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAATAA | 9678 |
rs2110376 | snp | G/T | 0.499722 | 0.0117779 | intron-variant | PHF14 | GRCh38.p7 | 7:10990005 | AGAGAACTCTATTAA[G/T]TAGGTCTCTATCAAG | 9678 |
rs2110377 | snp | G/T | 0.234401 | 0.249513 | intron-variant | PHF14 | GRCh38.p7 | 7:10989998 | TCTATTAAGTAGGTC[G/T]CTATCAAGAAATATC | 9678 |
rs2158780 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11045290 | GAAATTTGATCACTA[A/G]AAACAAGGAGAAATT | 9678 |
rs2160059 | snp | C/T | 0.189261 | 0.242509 | intron-variant | PHF14 | GRCh38.p7 | 7:10990121 | GCATTATCAAACTAC[C/T]GTAAGACAGATCCAT | 9678 |
rs2190293 | snp | C/T | 0.493658 | 0.0559517 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104451 | TTCTCCTTATAGTAG[C/T]TGGACCGATTATGGA | 9678 |
rs2190294 | snp | C/T | 0.436408 | 0.16659 | intron-variant | PHF14 | GRCh38.p7 | 7:11051110 | GAGGCTGCAGTGAGC[C/T]ATGATCTCAACACTG | 9678 |
rs2190295 | snp | G/T | 0.441158 | 0.161117 | intron-variant | PHF14 | GRCh38.p7 | 7:11050834 | AAAAAGGTCATATTA[G/T]TTGGTGGCCCCTACT | 9678 |
rs2214858 | snp | A/G | 0.437259 | 0.165632 | intron-variant | PHF14 | GRCh38.p7 | 7:11050919 | TTTTAATTGTAGTCA[A/G]TGACAACTTGTGCTG | 9678 |
rs2301959 | snp | C/G | 0.497959 | 0.0318836 | intron-variant | PHF14 | GRCh38.p7 | 7:11061679 | TAACTAATTTTGCAA[C/G]TGCCTAACCTAAGCA | 9678 |
rs2301960 | snp | C/T | 0.0221176 | 0.102809 | intron-variant | PHF14 | GRCh38.p7 | 7:11028840 | GAACATGTTCACCAA[C/T]TATGGGTTTAAATAA | 9678 |
rs2301961 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11023147 | ATAGAAGAATTTATG[C/T]ATTATTGGCTTTCTA | 9678 |
rs2301962 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11022793 | ACAAACATATAAAAC[A/G]CTTGCCATCTCAAAA | 9678 |
rs2353338 | snp | C/T | 0.255503 | 0.249939 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959648 | TTCCAGGTGCCAGCA[C/T]AGGCACCGGCTCTCT | 9678 |
rs2353339 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11001666 | TTTTAATTTCAATTC[C/T]ACTTGTTCATTGCTT | 9678 |
rs2353340 | snp | A/G | 0.487572 | 0.0778428 | intron-variant | PHF14 | GRCh38.p7 | 7:11035636 | CTGTGCTTTCTTTGT[A/G]TAGGATATAGCAGAT | 9678 |
rs2353341 | snp | C/G | 0.494568 | 0.0518327 | intron-variant | PHF14 | GRCh38.p7 | 7:11055452 | ACTCTCTTTGAAGTT[C/G]TGAGATCTTTCTTCC | 9678 |
rs2353342 | snp | G/T | 0.495521 | 0.0471118 | intron-variant | PHF14 | GRCh38.p7 | 7:11055482 | CTGACTTACAAATTC[G/T]GGTTGTGTTTTATAT | 9678 |
rs2353343 | snp | C/T | 0.180383 | 0.240111 | intron-variant | PHF14 | GRCh38.p7 | 7:11057086 | ATTAATTTGTATAAA[C/T]ATTGATATGTCAACA | 9678 |
rs2353344 | snp | A/C | 0.499741 | 0.0113788 | intron-variant | PHF14 | GRCh38.p7 | 7:11072620 | AAAAAATGGTAAAGG[A/C]TATATATATGCAAAT | 9678 |
rs2353791 | snp | C/T | 0.499121 | 0.020948 | intron-variant | PHF14 | GRCh38.p7 | 7:11163053 | ATTATTTATTAATAG[C/T]AAATATTTTTTAAAT | 9678 |
rs2353794 | snp | G/T | 0.259951 | 0.249802 | intron-variant | PHF14 | GRCh38.p7 | 7:11151313 | GTAATCCGAACACTT[G/T]GGGAAGCTGAAGTGG | 9678 |
rs2539823 | snp | C/G | 0.43978 | 0.162738 | intron-variant | PHF14 | GRCh38.p7 | 7:10991428 | AACACCTTGGGTGGC[C/G]AAGGCGGGTGGATCA | 9678 |
rs2625440 | snp | A/T | 0.497613 | 0.0344622 | intron-variant | PHF14 | GRCh38.p7 | 7:10991261 | TCTTAGCTCACTTCA[A/T]CCTCCGCCTCCTGGG | 9678 |
rs2883140 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056404 | TTAGACCCATAGTTA[G/T]TTCAGTTTATAGTAG | 9678 |
rs2883141 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065433 | CAGAAAATGCTTGGT[A/T]AATGAACTCTACATA | 9678 |
rs2906543 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | PHF14 | GRCh38.p7 | 7:11093730 | agaaccaagcttgtg[A/G]ttctttggaggctga | 9678 |
rs2906544 | snp | A/G | 0.492287 | 0.0616198 | intron-variant | PHF14 | GRCh38.p7 | 7:11093580 | ttcttcagtagcaca[A/G]gcatacagagaaagg | 9678 |
rs2906545 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | PHF14 | GRCh38.p7 | 7:11093471 | agaaatccaaagaaa[C/T]ctgaagccttgtggt | 9678 |
rs2906546 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | PHF14 | GRCh38.p7 | 7:11092978 | GGGAGACAACAGACA[A/G]AGTGCTATTTCAGAG | 9678 |
rs2906547 | snp | A/C | 0.492287 | 0.0616198 | intron-variant | PHF14 | GRCh38.p7 | 7:11092705 | CTCACATTAGAACAA[A/C]AAAAAAAGAGACTTC | 9678 |
rs2906548 | snp | C/T | 0.492533 | 0.0606443 | intron-variant | PHF14 | GRCh38.p7 | 7:11092041 | GGCAGAGTATTAAAA[C/T]CTCATCTTGAGGCTC | 9678 |
rs2906549 | snp | A/T | 0.492727 | 0.0598633 | intron-variant | PHF14 | GRCh38.p7 | 7:11091499 | CAAAGTGCTGGGGTT[A/T]CAGGCGTGAGCAACG | 9678 |
rs2906550 | snp | A/G | 0.493107 | 0.0583 | intron-variant | PHF14 | GRCh38.p7 | 7:11091417 | AAAATGTCTAATTCA[A/G]TAGACCTTTAAAAAA | 9678 |
rs2906551 | snp | A/G | 0.446641 | 0.154377 | intron-variant | PHF14 | GRCh38.p7 | 7:11091276 | CAGTTTGCTTTAAAC[A/G]CTTCCCTTTCTTCCT | 9678 |
rs2906552 | snp | A/G | 0.493386 | 0.0571263 | intron-variant | PHF14 | GRCh38.p7 | 7:11091203 | TGATGTTATGTTTCC[A/G]AGATCTTTCTAATCC | 9678 |
rs2906553 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | PHF14 | GRCh38.p7 | 7:11091037 | CAATAAATCTCCATT[A/G]GACCCCTTAACATCA | 9678 |
rs2906554 | snp | C/G | 0.49334 | 0.057322 | intron-variant | PHF14 | GRCh38.p7 | 7:11089866 | GGAGAATCGCTTGAA[C/G]CCAGGAGGTGGAGTT | 9678 |
rs2906555 | snp | C/G | 0.492727 | 0.0598633 | intron-variant | PHF14 | GRCh38.p7 | 7:11089219 | TGTTGTTTTGAGGAA[C/G]AGATTTGATGTTTAT | 9678 |
rs2906556 | snp | A/G | 0.492435 | 0.0610346 | intron-variant | PHF14 | GRCh38.p7 | 7:11088776 | CTCCCCTCCTATACA[A/G]TGTTTTCAGTTGTTT | 9678 |
rs2906557 | snp | A/C | 0.446771 | 0.154211 | intron-variant | PHF14 | GRCh38.p7 | 7:11087402 | GAGTTCGAGACCAGT[A/C]TGGCCAACATGGTGA | 9678 |
rs2906558 | snp | A/G | 0.478603 | 0.101197 | intron-variant | PHF14 | GRCh38.p7 | 7:11086883 | CCCAAGAGGACTAAG[A/G]GTAATAAAACTCAAG | 9678 |
rs2906559 | snp | A/G | 0.483126 | 0.0902898 | intron-variant | PHF14 | GRCh38.p7 | 7:11086432 | TTTCAGAGAGAAGGT[A/G]TAACATAAAGTATAA | 9678 |
rs2906560 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | PHF14 | GRCh38.p7 | 7:11086094 | AGTTGATGAAGGAGA[A/G]TAAGCACTACATATT | 9678 |
rs2906561 | snp | A/G | 0.479583 | 0.0989539 | intron-variant | PHF14 | GRCh38.p7 | 7:11086024 | AAGATTATTATCCTC[A/G]GTTTACAGATGAGGA | 9678 |
rs2906562 | snp | C/T | 0.479258 | 0.0997024 | intron-variant | PHF14 | GRCh38.p7 | 7:11085492 | CTACAATAGAAACAA[C/T]AATTTTTGCCTTTAG | 9678 |
rs2906563 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | PHF14 | GRCh38.p7 | 7:11085489 | CAATAGAAACAATAA[C/T]TTTTGCCTTTAGAAT | 9678 |
rs2906564 | snp | A/C | 0.499872 | 0.0079862 | intron-variant | PHF14 | GRCh38.p7 | 7:11084549 | AACTGGCTTAGTTCT[A/C]TATTTACTGAGAAAA | 9678 |
rs2906565 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | PHF14 | GRCh38.p7 | 7:11084399 | TAGAGGAAAGAAGTA[C/T]GGATGATGATATACT | 9678 |
rs2906566 | snp | A/G | 0.49533 | 0.0480965 | intron-variant | PHF14 | GRCh38.p7 | 7:11083939 | CCTATTGCCCCAGAC[A/G]GGCATCCCATCTTCT | 9678 |
rs2995878 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | PHF14 | GRCh38.p7 | 7:11093383 | ctgactcaactcccc[C/T]atactaacagccttg | 9678 |
rs2995879 | snp | C/T | 0.494143 | 0.0537956 | intron-variant | PHF14 | GRCh38.p7 | 7:11093189 | aagatgcaattaaac[C/T]agaaatcattagcag | 9678 |
rs2995880 | snp | C/T | 0.492582 | 0.0604491 | intron-variant | PHF14 | GRCh38.p7 | 7:11093152 | atatggaaaatcctc[C/T]gaatatttggaaata | 9678 |
rs2995881 | snp | A/T | 0.445328 | 0.156035 | intron-variant | PHF14 | GRCh38.p7 | 7:11092407 | AGTGATTGCCATAGT[A/T]TAGTCTCCAGACCAG | 9678 |
rs2995884 | snp | A/C | 0.489893 | 0.0703642 | intron-variant | PHF14 | GRCh38.p7 | 7:11089250 | AATTACATACGCAAA[A/C]AGCTGATAACTTTAA | 9678 |
rs2995885 | snp | G/T | 0.475437 | 0.108066 | intron-variant | PHF14 | GRCh38.p7 | 7:11088403 | CGTGTGTGTGTGTGT[G/T]TGTGTGTATGTGAAC | 9678 |
rs2995886 | snp | C/T | 0.480382 | 0.097079 | intron-variant | PHF14 | GRCh38.p7 | 7:11088102 | GGACTTGAGCATCTT[C/T]AGATTTTGATATCCG | 9678 |
rs2995898 | snp | C/T | 0.478603 | 0.101197 | intron-variant | PHF14 | GRCh38.p7 | 7:11086690 | CCCATTAATATCTGA[C/T]AATTATAACTTTTAA | 9678 |
rs2995901 | snp | C/T | 0.479502 | 0.0991411 | intron-variant | PHF14 | GRCh38.p7 | 7:11085601 | GAGGAAGGTTGGTCA[C/T]CAATGTTAAATGTTG | 9678 |
rs2995902 | snp | C/T | 0.499999 | 0.000798721 | intron-variant | PHF14 | GRCh38.p7 | 7:11085196 | ATCTTTAAAACATGT[C/T]AAGCAAAACTGTACA | 9678 |
rs2995903 | snp | C/T | 0.440195 | 0.162252 | intron-variant | PHF14 | GRCh38.p7 | 7:11084901 | TCTCCAAAGATAAAG[C/T]GGCAAAGGATATGGA | 9678 |
rs3073107 | in-del | -/GAA/GAAA | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11072702 | TTACATTGCTATAAA[-/GAA/GAAA]TACCTGAGGCTAGCT | 9678 |
rs3073111 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075590 | TTTTTTTTTTTTTTT[-/T]ATTATTATGCCATTC | 9678 |
rs3779409 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11033598 | CATAGGGGTCTAGTA[C/T]TAATGGGAAGAATGG | 9678 |
rs3779410 | snp | A/G | 0.097727 | 0.198275 | intron-variant | PHF14 | GRCh38.p7 | 7:11046174 | GTTTATGTTATTTTG[A/G]TTTTTGTTGTTGTTT | 9678 |
rs3801434 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11021347 | GTTATAAATAATGTG[C/T]ATCTAAACAGATGAG | 9678 |
rs3801435 | snp | A/G | 0.496175 | 0.0435625 | intron-variant | PHF14 | GRCh38.p7 | 7:11021599 | CTGTTAGGTTTATCA[A/G]AGATAAACTCCTACA | 9678 |
rs3801437 | snp | A/G | 0.437401 | 0.165472 | intron-variant | PHF14 | GRCh38.p7 | 7:11030107 | TCTTGATTTTAAGGA[A/G]TTGTACTTTGATGAA | 9678 |
rs3801438 | snp | A/G | 0.158302 | 0.232576 | intron-variant | PHF14 | GRCh38.p7 | 7:11030227 | GCTACAACTCAGGAT[A/G]GTGGGCAAAAGTACG | 9678 |
rs3801439 | snp | C/G | 0.0652144 | 0.168387 | intron-variant | PHF14 | GRCh38.p7 | 7:11045574 | CACTTGCTATCCAGC[C/G]TTTTCTTCCAGTACC | 9678 |
rs3801440 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | PHF14 | GRCh38.p7 | 7:11051853 | GAGTGAGAAAGACAC[A/G]GGGCAAACATATACT | 9678 |
rs3801441 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | PHF14 | GRCh38.p7 | 7:11054082 | CTATTCTTTTTCTTA[A/G]CTTGTTTTTATCAAA | 9678 |
rs3801442 | snp | A/G | 0.00399207 | 0.0444983 | intron-variant | PHF14 | GRCh38.p7 | 7:11056004 | ATTTGTGGGGGCTTT[A/G]CATACCAGAGTTTTC | 9678 |
rs3801443 | snp | A/G | 0.0655868 | 0.168795 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062722 | CATTGGCTTTTCCCA[A/G]CGGTCCAGAGGCTGC | 9678 |
rs3801444 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | PHF14 | GRCh38.p7 | 7:11080311 | TACACGTGCATACTT[A/G]TTAACATCTCACTTT | 9678 |
rs3801445 | snp | A/T | 0.0930568 | 0.194599 | intron-variant | PHF14 | GRCh38.p7 | 7:11080559 | TTAGATTCAGTTTTT[A/T]AATAAACATTAACTC | 9678 |
rs3801449 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | PHF14 | GRCh38.p7 | 7:11096154 | GTTCTTTTATTCTTT[C/T]TCGGTGTCTGAGTAT | 9678 |
rs3801450 | snp | A/G | 0.494057 | 0.0541878 | intron-variant | PHF14 | GRCh38.p7 | 7:11096282 | TCTTTATCAGTAACT[A/G]TCATCAAAAAAATTT | 9678 |
rs3801451 | snp | C/G | 0.491629 | 0.0641526 | intron-variant | PHF14 | GRCh38.p7 | 7:11099093 | ATGAGTGTAGCCCAG[C/G]TGCCACTGAATTTTT | 9678 |
rs3801452 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11099172 | TGGTATATTTTTTCT[A/G]TAATTAAGTTGATTT | 9678 |
rs3801453 | snp | A/G | 0.491104 | 0.0660973 | intron-variant | PHF14 | GRCh38.p7 | 7:11101156 | TTAGGATGTAGGGAT[A/G]TTAGCAATAGCTTTT | 9678 |
rs3801454 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11101242 | ATATCTAATGTGTCT[A/G]TATTCGGATGCATTT | 9678 |
rs3801455 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103595 | GAATTGCACTTATAC[A/G]TGTAAATTGTCAACA | 9678 |
rs3801456 | snp | G/T | 0.0799831 | 0.183287 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103629 | AATTTGGAATTTTCT[G/T]ATTAATAAATGTGGT | 9678 |
rs3815234 | snp | A/C/T | 0.164219 | 0.234823 | intron-variant | PHF14 | GRCh38.p7 | 7:11023179 | TTACCTCATACGTTA[A/C/T]TCTAAATTAAGAATG | 9678 |
rs3823874 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11045336 | TCCTGTTACTGGACT[C/G]TTATTTCATGACTGT | 9678 |
rs3823875 | snp | A/G | 0.450105 | 0.149859 | intron-variant | PHF14 | GRCh38.p7 | 7:11045797 | GTGATATAGGAGTCT[A/G]TTGAGAGGGAAGAGA | 9678 |
rs3834728 | in-del | -/G | 0.0693013 | 0.172766 | intron-variant | PHF14 | GRCh38.p7 | 7:10990565 | ATAATGTACTTTGAA[-/G]TTAATAAAAGAATGG | 9678 |
rs3839758 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021677 | AAATTAAATTGAGAA[-/A]GCAGCTGCTTGTTGA | 9678 |
rs3839760 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046645 | CTGCTATTAAAGTTT[-/T]ATACAGGTATTATAA | 9678 |
rs3839761 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055824 | TGAAAATATGAAATA[-/T]GTTTCATATAAATAT | 9678 |
rs3839763 | in-del | -/T | 0.496874 | 0.0394129 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063053 | CCAAATGATTTAATC[-/T]TATTTTGGTCATTAA | 9678 |
rs3840624 | in-del | -/GTGCCAAGGCGGAGCAGAGATCC | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973700 | GCGGAGCAGAGATCC[-/GTGCCAAGGCGGAGCAGAGATCC]CCGCCAAACCCTGTG | 9678 |
rs4030735 | in-del | -/CCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072545 | acaatagtacctact[-/CCA]tagattgtctggatg | 9678 |
rs4314555 | snp | A/G | 0.49423 | 0.0534032 | intron-variant | PHF14 | GRCh38.p7 | 7:11109730 | ATGCCAGAACAACAG[A/G]TATTTGAACATTTTA | 9678 |
rs4342485 | snp | C/T | 0.440333 | 0.16209 | intron-variant | PHF14 | GRCh38.p7 | 7:11018860 | ttttcccattcagta[C/T]gatactagctgtggg | 9678 |
rs4348382 | snp | A/G | 0.327914 | 0.237549 | intron-variant | PHF14 | GRCh38.p7 | 7:10995471 | gtccccactagactc[A/G]ggagcctagctggct | 9678 |
rs4370426 | snp | A/C | 0.49917 | 0.0203505 | intron-variant | PHF14 | GRCh38.p7 | 7:11023675 | ctactaaaaatacaa[A/C]aaattagctgggcgt | 9678 |
rs4385368 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | PHF14 | GRCh38.p7 | 7:10980952 | TAAGAGTGTTTTTTT[C/G]AGAACAGTCCCAAGT | 9678 |
rs4398795 | snp | C/T | 0.338069 | 0.233974 | intron-variant | PHF14 | GRCh38.p7 | 7:10994656 | cttcaagaatgaagc[C/T]gtggatcctcgcggt | 9678 |
rs4495316 | snp | A/G | 0.444 | 0.157683 | intron-variant | PHF14 | GRCh38.p7 | 7:11152873 | ATAAAAGTCAGAGGA[A/G]ACACCTACTGCATTT | 9678 |
rs4521663 | snp | A/T | 0.34214 | 0.262612 | intron-variant | PHF14 | GRCh38.p7 | 7:10994983 | ccacatcctgctgat[A/T]ggtccattttacaga | 9678 |
rs4534044 | snp | A/C | 0.491157 | 0.065903 | intron-variant | PHF14 | GRCh38.p7 | 7:11109098 | TACTTAACTCAGTAG[A/C]AATTATCATTTTCAT | 9678 |
rs4554366 | snp | C/G | 0.0249007 | 0.109157 | intron-variant | PHF14 | GRCh38.p7 | 7:10995061 | tccctgagatagaca[C/G]aaaagttctccaagt | 9678 |
rs4644135 | snp | G/T | 0.495891 | 0.0451408 | intron-variant | PHF14 | GRCh38.p7 | 7:11136664 | TCTTAATCATGTGTA[G/T]TTCACTTTGTACACA | 9678 |
rs4719258 | snp | G/T | 0.498693 | 0.0255257 | intron-variant | PHF14 | GRCh38.p7 | 7:11132279 | ACTGATAACCAGGGT[G/T]TTGTTCTGTCTGTAT | 9678 |
rs4719259 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11132477 | tatataccacaattt[A/C]tttacccatttgtct | 9678 |
rs4719260 | snp | A/G | 0.464523 | 0.128375 | intron-variant | PHF14 | GRCh38.p7 | 7:11164169 | TTTTACTGTTGTACC[A/G]CCATGGATGTTTGCC | 9678 |
rs4720925 | snp | A/G | 0.272241 | 0.249009 | intron-variant | PHF14 | GRCh38.p7 | 7:10978768 | TCCACTTCCACTGTT[A/G]TGGCAACTATTGTTT | 9678 |
rs4720927 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11003741 | AATTAATTCATTAAA[A/G]TATTCTTAATTATAA | 9678 |
rs4720932 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PHF14 | GRCh38.p7 | 7:11054499 | ATACAGAAGGGAGTG[A/G]TCAGTCATTTTGGTC | 9678 |
rs4720933 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11075375 | acggatctgccggct[A/G]tacaagcagcatggc | 9678 |
rs4720934 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11088360 | tatggagggcagact[C/G]TATTAACTTCAGAAG | 9678 |
rs4720936 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11088533 | TTTTAAATGTCTTTT[A/T]TAAATGTATTTCATT | 9678 |
rs4720938 | snp | G/T | 0.487432 | 0.0782705 | intron-variant | PHF14 | GRCh38.p7 | 7:11127155 | CAGTTTAATGTCAAA[G/T]CTTCTATTCTCAGCA | 9678 |
rs4720939 | snp | A/C/G | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11127562 | AGACAGGCATGTATC[A/C/G]TCATCTAGTCCTTGT | 9678 |
rs4720941 | snp | A/T | 0.45946 | 0.136478 | intron-variant | PHF14 | GRCh38.p7 | 7:11132620 | ttcctagaagaggga[A/T]tctgggtcatatggt | 9678 |
rs5882292 | in-del | -/T | 0.49263 | 0.0602539 | intron-variant | PHF14 | GRCh38.p7 | 7:11092100 | TACCTCTGTGTATAA[-/T]ATAATACTTATCTCT | 9678 |
rs5882293 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137611 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTTTTGC | 9678 |
rs5882294 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11162718 | TTTTTTTTTTTTTTT[-/T]GATATGGAGTTTCGG | 9678 |
rs6460784 | snp | C/T | 0.235564 | 0.249583 | intron-variant | PHF14 | GRCh38.p7 | 7:11083701 | ctcctgacctcgtga[C/T]ccacccccttggcct | 9678 |
rs6460785 | snp | A/G | 0.447291 | 0.153545 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106656 | ATGAAAGAACTCATC[A/G]CTACCTGTTAATAGA | 9678 |
rs6460787 | snp | A/T | 0.124144 | 0.21601 | intron-variant | PHF14 | GRCh38.p7 | 7:11144011 | gaacatacctggaac[A/T]ctaacaactcaacag | 9678 |
rs6460789 | snp | C/T | 0.463234 | 0.130503 | intron-variant | PHF14 | GRCh38.p7 | 7:11156331 | TCAATTTCTTTTTAA[C/T]CCATGAAAAATTAAT | 9678 |
rs6460790 | snp | A/C | 0.47666 | 0.105476 | intron-variant | PHF14 | GRCh38.p7 | 7:11160326 | gcacctaggttgatt[A/C]catgtcttcgctatt | 9678 |
rs6943167 | snp | A/G | 0.175254 | 0.238565 | intron-variant | PHF14 | GRCh38.p7 | 7:11007134 | ggaggcggagattgc[A/G]gtgagccgagatcgc | 9678 |
rs6943233 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | PHF14 | GRCh38.p7 | 7:11014405 | CTGGGCCTGAGGGAG[A/T]TTATCCAAGGAATGA | 9678 |
rs6943346 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | PHF14 | GRCh38.p7 | 7:10998004 | gctgcctaccacatg[G/T]gcagagattatatag | 9678 |
rs6943379 | snp | C/T | 0.439918 | 0.162576 | intron-variant | PHF14 | GRCh38.p7 | 7:11028155 | aatatgcttggaaca[C/T]ttacattagcctaca | 9678 |
rs6943604 | snp | A/C | 0.450609 | 0.149185 | intron-variant | PHF14 | GRCh38.p7 | 7:10984565 | GTTAATACTCTATAT[A/C]TAATGAATAAGTTTA | 9678 |
rs6943989 | snp | G/T | 0.448708 | 0.151707 | intron-variant | PHF14 | GRCh38.p7 | 7:10984521 | TGTTTGTATTTAATT[G/T]AGGCATGCATGCAGT | 9678 |
rs6945159 | snp | A/G | 0.101658 | 0.201233 | intron-variant | PHF14 | GRCh38.p7 | 7:11150437 | ATGGAAATCACCTCT[A/G]TTCTCCTCCCTGTCC | 9678 |
rs6945372 | snp | A/G | 0.458084 | 0.138567 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972447 | TTTATAATTTCATAG[A/G]TAAGACTATCAGTCC | 9678 |
rs6945716 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11141567 | TTTGATATAAATTAT[C/T]TTAAAATGTTCCTGG | 9678 |
rs6945835 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965238 | atgttggtgacctac[A/G]gatgtggttttggtg | 9678 |
rs6946317 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:10986686 | GTCTTTTTCAGCCGT[C/T]AATCTTGCAGCTTTG | 9678 |
rs6946657 | snp | A/T | 0.0239773 | 0.106835 | intron-variant | PHF14 | GRCh38.p7 | 7:11068703 | tatattttaccacaa[A/T]tgaTTTTTAAAAATA | 9678 |
rs6949224 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11156645 | ctaaaaaatacaaaa[A/G]ttagccgggtgtagt | 9678 |
rs6949600 | snp | A/T | 0.040671 | 0.13668 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063064 | TAATCTATTTTGGTC[A/T]TTAAAATATGTCTTA | 9678 |
rs6950133 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973058 | tcactttgtaacttc[A/G]ccatctgcaagaaat | 9678 |
rs6950505 | snp | C/T | 0.338296 | 0.233889 | intron-variant | PHF14 | GRCh38.p7 | 7:10994129 | aacgagcactgcaag[C/T]ggagggagtagtgaa | 9678 |
rs6951215 | snp | G/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105261 | TCATTCGTTGTTGCT[G/T]AAGTGTTCATCTGAT | 9678 |
rs6951511 | snp | C/G | 0.0715223 | 0.175059 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962869 | tttatttgcacagag[C/G]tgtttatagtattct | 9678 |
rs6951535 | snp | C/T | 0.130008 | 0.219321 | intron-variant | PHF14 | GRCh38.p7 | 7:10996658 | TAAATATAAAATACA[C/T]AGAAGCAAGGGGAAA | 9678 |
rs6952822 | snp | C/G | 0.476314 | 0.106217 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963600 | ttaggtttgcttggt[C/G]cagagctgagtccaa | 9678 |
rs6953496 | snp | A/C | 0.47517 | 0.10862 | intron-variant | PHF14 | GRCh38.p7 | 7:11156821 | AAAAGAAAAGAAATT[A/C]ACTTTCTACACTTAA | 9678 |
rs6954256 | snp | C/T | 0.167484 | 0.23599 | intron-variant | PHF14 | GRCh38.p7 | 7:11074131 | tgtctcttttttagt[C/T]atgctaatcacttta | 9678 |
rs6954805 | snp | G/T | 0.491473 | 0.0647364 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104403 | AATAATCTCTTAAAT[G/T]CTCTCATATCCACAG | 9678 |
rs6955020 | snp | A/G | 0.175254 | 0.238565 | intron-variant | PHF14 | GRCh38.p7 | 7:10979634 | CAGCCTATGGAAAAA[A/G]TAGCCAAGGGCCTTG | 9678 |
rs6955289 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | PHF14 | GRCh38.p7 | 7:11151990 | CCACAATAAATCCTA[A/C]ATATTTTCAGAATAG | 9678 |
rs6955372 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PHF14 | GRCh38.p7 | 7:11151900 | TATGTTCCTCAGAAG[C/T]TGATCCTTGTACATT | 9678 |
rs6956108 | snp | A/G | 0.192715 | 0.243348 | intron-variant | PHF14 | GRCh38.p7 | 7:10996927 | ATCTACTCAACAGCC[A/G]TAGGTTTTATTTTTA | 9678 |
rs6957940 | snp | C/G | 0.440333 | 0.16209 | intron-variant | PHF14 | GRCh38.p7 | 7:11110028 | TGCTTAACTTTTCTG[C/G]AACTCTTGATTCCCC | 9678 |
rs6958196 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PHF14 | GRCh38.p7 | 7:11052470 | taaatatctcctgca[A/G]catggtaacaaggag | 9678 |
rs6958214 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11071134 | tgtcacttgccagct[C/T]tgtaattttaagcaa | 9678 |
rs6958458 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957541 | CCCCTTGTGAAAAAC[A/G]TCTCCAAAGCCTGCC | 9678 |
rs6958816 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11157705 | CGTTTAAAAACATGA[A/C]AATGAATTTCATGTG | 9678 |
rs6961592 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11144373 | tactgggtatttatc[A/T]aaaggaaaataaatt | 9678 |
rs6965290 | snp | C/T | 0.17654 | 0.238964 | intron-variant | PHF14 | GRCh38.p7 | 7:11055238 | TTACCCATATCCCTT[C/T]TGAAGTTACTTTAAA | 9678 |
rs6967485 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11050690 | tattataaaaagttc[A/T]gttggataccactTG | 9678 |
rs6967802 | snp | A/T | 0.0528381 | 0.153711 | intron-variant | PHF14 | GRCh38.p7 | 7:11046872 | TAGACATAAGAAAAA[A/T]AAAAACTCTGGTGTG | 9678 |
rs6968254 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PHF14 | GRCh38.p7 | 7:11081991 | ACTGGTTTTTAAAAG[C/T]TAATAGTGTACGTAG | 9678 |
rs6968425 | snp | A/C | 0.439502 | 0.163061 | intron-variant | PHF14 | GRCh38.p7 | 7:11082180 | gagaccttgtctcta[A/C]taaaatttttaaaaa | 9678 |
rs6968626 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PHF14 | GRCh38.p7 | 7:11082003 | AAGCTAATAGTGTAC[A/G]TAGAATTCTAACAGA | 9678 |
rs6968691 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PHF14 | GRCh38.p7 | 7:11017265 | tttcggatgtatacc[C/T]aacagtgcagttgct | 9678 |
rs6968797 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11142307 | TTCTGTTCTTATAGT[A/G]ATACACATAGCAATT | 9678 |
rs6969350 | snp | A/G | 0.492087 | 0.0623997 | intron-variant | PHF14 | GRCh38.p7 | 7:11112591 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 9678 |
rs6970208 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PHF14 | GRCh38.p7 | 7:11004995 | gcactccagcctggg[C/T]aatagagcgagattc | 9678 |
rs6970876 | snp | C/T | 0.339882 | 0.233284 | intron-variant | PHF14 | GRCh38.p7 | 7:11012651 | GCCAAGTTATCTTGT[C/T]TGTTGGGTGTGTTCA | 9678 |
rs6971440 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11060066 | attgttagtagagat[A/G]aggtctctctgtgtt | 9678 |
rs6971841 | snp | G/T | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:11078706 | TCGTATTTTTAAAGT[G/T]TTGTTCTTATTTATA | 9678 |
rs6972232 | snp | C/G | 0.039522 | 0.134904 | intron-variant | PHF14 | GRCh38.p7 | 7:11148106 | ATTACAGTACtccaa[C/G]ttaccatcattcctg | 9678 |
rs6972430 | snp | A/T | 0.203267 | 0.245593 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956399 | ATTTGAGGAAGATTT[A/T]AAAAAATTACTTGAT | 9678 |
rs6972528 | snp | A/T | 0.110167 | 0.207236 | intron-variant | PHF14 | GRCh38.p7 | 7:11109236 | AATATCAGGAAGCAG[A/T]GGCTGATAGTTTTCA | 9678 |
rs6973228 | snp | C/T | 0.440884 | 0.161442 | intron-variant | PHF14 | GRCh38.p7 | 7:11017799 | cgtctgtttttgctt[C/T]ggttgcttgtgcttg | 9678 |
rs6973733 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11018001 | gcagtttttccagca[C/T]catttgttgaagaaa | 9678 |
rs6974192 | snp | C/T | 0.16846 | 0.236329 | intron-variant | PHF14 | GRCh38.p7 | 7:11076031 | gtagttccagctact[C/T]gggaggctgaggcag | 9678 |
rs6974846 | snp | G/T | 0.16846 | 0.236329 | intron-variant | PHF14 | GRCh38.p7 | 7:11076288 | GTTAAAGGCTAAATG[G/T]TGGCATCCCTTCCGT | 9678 |
rs6975314 | snp | C/T | 0 | 0 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973772 | gggctttcactcggc[C/T]ctgttcggctcctgc | 9678 |
rs6975761 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11152173 | TCTGGTCAGTATCCA[C/T]TGAGCAAAAATTGGA | 9678 |
rs6975914 | snp | C/T | 0.104149 | 0.203046 | intron-variant | PHF14 | GRCh38.p7 | 7:11013387 | ggctggtctcgaact[C/T]ctcacctcaggtgat | 9678 |
rs6976070 | snp | A/G | 0.182614 | 0.240747 | intron-variant | PHF14 | GRCh38.p7 | 7:11006044 | tgatctgcccacctc[A/G]gcctcccaaagtgct | 9678 |
rs6977077 | snp | A/T | 0.0111196 | 0.0737302 | | | GRCh38.p7 | 7:10970891 | atactatattgaaaa[A/T]ataaagtacaaaaat | 9678 |
rs6979420 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11144139 | aatcgctaatcatca[A/G]ggaattgcaaatcaa | 9678 |
rs6980126 | snp | A/G | 0.0244538 | 0.107838 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107219 | TATTCTCAATAGTCA[A/G]GTAAACACCTGACTA | 9678 |
rs7350022 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11053413 | ATAACTCTTTTTTTA[A/G]GCTTCAAAAATATAT | 9678 |
rs7350023 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11053440 | ATATTTTGTTTATAA[A/G]GGAACTAGAGAGACT | 9678 |
rs7357144 | snp | C/G | 0.0256215 | 0.110247 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973027 | ttgcaggagagtctt[C/G]ctttgcatagaagta | 9678 |
rs7357146 | snp | C/T | 0.187685 | 0.242109 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973225 | gttggctgctttctg[C/T]aaccaatcagactga | 9678 |
rs7457424 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023303 | TAAGCCTAATTTCTG[A/T]CTTTACTTTTGAAGT | 9678 |
rs7779388 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | PHF14 | GRCh38.p7 | 7:11081295 | gcatgacaatactat[C/T]tgtaaagtaacagca | 9678 |
rs7780549 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11020038 | AATTTTTAAAAATAA[C/G]CTTTATGTTGCAATA | 9678 |
rs7780730 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11020192 | ctcctgggctcaggt[C/G]atcctcccactgaag | 9678 |
rs7781258 | snp | A/G | 0.446118 | 0.155041 | intron-variant | PHF14 | GRCh38.p7 | 7:11108305 | TATATTTGTATATTT[A/G]TTTATCACCAAAACT | 9678 |
rs7781934 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11155773 | CAATGTTTTTTTTTT[G/T]TTTTTTTTTAGCAAC | 9678 |
rs7782589 | snp | A/G | 0.49655 | 0.04139 | intron-variant | PHF14 | GRCh38.p7 | 7:11073392 | cccagccaggcatac[A/G]ttaaaccttaaaagc | 9678 |
rs7783877 | snp | C/T | 0.031825 | 0.122064 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965816 | ggactcccttccccc[C/T]accatgctccagcgt | 9678 |
rs7784204 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10996220 | ctaaggtgggaaact[A/G]ggaaaatatttagga | 9678 |
rs7785008 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | PHF14 | GRCh38.p7 | 7:11108701 | GCTGAAAGATAATTT[A/G]ATTGTACGAGTAGTT | 9678 |
rs7786061 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | PHF14 | GRCh38.p7 | 7:11167182 | GCTAGAGAAAACTAG[A/G]TAGCCAAGCATGTTA | 9678 |
rs7786566 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | PHF14 | GRCh38.p7 | 7:11079664 | CAAGCACTAAATTCT[A/G]TAATATGACTCTCTG | 9678 |
rs7786922 | snp | A/G | 0.465158 | 0.127307 | intron-variant | PHF14 | GRCh38.p7 | 7:11167468 | GCATACCTTTTATTC[A/G]TTCATTATTCCACTG | 9678 |
rs7788474 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11097469 | TCACCATTAGGCGTA[G/T]TAGTAGGCCTTTATC | 9678 |
rs7789137 | snp | C/T | 0.166832 | 0.235761 | intron-variant | PHF14 | GRCh38.p7 | 7:11027114 | TTTTCCTTATATTCA[C/T]TCTGAAATCCCTTGC | 9678 |
rs7789156 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11075766 | catttagatacccta[A/T]gaaataagtattaat | 9678 |
rs7789963 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | PHF14 | GRCh38.p7 | 7:10997673 | taagctaagtcaaat[A/G]gttgttggtaggctt | 9678 |
rs7790383 | snp | G/T | 0.494358 | 0.0528145 | intron-variant | PHF14 | GRCh38.p7 | 7:11130769 | gacacatgtccacca[G/T]tacagtgtcatacag | 9678 |
rs7790388 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | PHF14 | GRCh38.p7 | 7:11160865 | ccattctgtaggttg[A/T]ctgtttactctgttt | 9678 |
rs7790448 | snp | A/G | 0.42803 | 0.175514 | intron-variant | PHF14 | GRCh38.p7 | 7:11115624 | cagccagatcaggaa[A/G]ttaacattgctatat | 9678 |
rs7790568 | snp | C/T | 0.221439 | 0.248363 | intron-variant | PHF14 | GRCh38.p7 | 7:11100756 | ATTACTTGCCCAAGA[C/T]TGTACAACTGGAAAA | 9678 |
rs7791995 | snp | G/T | 0.492087 | 0.0623997 | intron-variant | PHF14 | GRCh38.p7 | 7:11015557 | AGTTGGACTGTCTAT[G/T]TTTGGATTCTAGTCT | 9678 |
rs7792131 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | PHF14 | GRCh38.p7 | 7:11127847 | AAATTTCACTCACCC[A/G]TGAGTCCTAAATCAA | 9678 |
rs7792168 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11080622 | AAGGGTTTACATTTA[A/G]TCAGCAATTCTTTGT | 9678 |
rs7792307 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:10979903 | GGGGTTGGGTAAGCT[A/T]TTAGGAGTTGGTTTT | 9678 |
rs7794114 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961133 | attgcttttggtgtt[C/T]tagtcatgaagtctt | 9678 |
rs7794514 | snp | A/T | 0.312348 | 0.242101 | intron-variant | PHF14 | GRCh38.p7 | 7:11123479 | CTCTTGAATTTTGAT[A/T]AACTTTAAAGCTAGA | 9678 |
rs7795751 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | PHF14 | GRCh38.p7 | 7:11131966 | CTTGTTGGGTTTTTT[A/T]AAAAATTTTTTattg | 9678 |
rs7795849 | snp | A/G | 0.175254 | 0.238565 | intron-variant | PHF14 | GRCh38.p7 | 7:11081063 | aatatatatgtatat[A/G]tgtgtgtgtgtattt | 9678 |
rs7798427 | snp | A/G | 0.482234 | 0.0925596 | intron-variant | PHF14 | GRCh38.p7 | 7:11159553 | TTCAAGCCAATCATA[A/G]TAAAGATGATTACCA | 9678 |
rs7800798 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11155774 | aatgttttttttttg[G/T]ttttttttagcaact | 9678 |
rs7800938 | snp | C/G/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11125755 | TGGACTATATTCATA[C/G/T]GATAAATCTAATCTC | 9678 |
rs7801080 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11135099 | TCTTAGATGTACTCA[A/G]TGTCCCTGTACTTTT | 9678 |
rs7802053 | snp | A/G | 0.252702 | 0.249985 | intron-variant | PHF14 | GRCh38.p7 | 7:11159813 | CAATTTATAGAAAGA[A/G]AAAATTCTAACAATA | 9678 |
rs7802913 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11130331 | CAAGACCTTTCTGGG[A/C]TTCATTCCAGGATTC | 9678 |
rs7803348 | snp | C/T | 0.492966 | 0.0588865 | intron-variant | PHF14 | GRCh38.p7 | 7:11130592 | ccctcatcccttcct[C/T]cttcccctagtttcc | 9678 |
rs7805731 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11112734 | cgagatcacgccatt[A/G]catgccaacctgggc | 9678 |
rs7806039 | snp | A/G | 0.493881 | 0.054972 | intron-variant | PHF14 | GRCh38.p7 | 7:11136052 | GTATACATAAGTAAC[A/G]TTGTTGAAAATAGTT | 9678 |
rs7806840 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | PHF14 | GRCh38.p7 | 7:11113612 | GACTTAATATACTAC[C/T]ATTTTCCAATGAAAA | 9678 |
rs7807585 | snp | A/C | 0.461259 | 0.133677 | intron-variant | PHF14 | GRCh38.p7 | 7:10975817 | ACAGTTTTTAAATAT[A/C]CTTCCAGAGAGTTTG | 9678 |
rs7808367 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11152482 | ATAATATATTTGTAA[C/T]ATATTCTGTATATAG | 9678 |
rs7809178 | snp | C/T | 0.437259 | 0.165632 | intron-variant | PHF14 | GRCh38.p7 | 7:11115668 | tcctcagatttcatt[C/T]aggtttggctattaa | 9678 |
rs7810016 | snp | A/G | 0.171057 | 0.237209 | intron-variant | PHF14 | GRCh38.p7 | 7:11031310 | TCCTTTATCTCATTG[A/G]TGAGAATCCATGTGA | 9678 |
rs7810327 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960740 | tctccacatcctctc[C/T]agcatctgttgtttc | 9678 |
rs7810668 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11015576 | GGATTCTAGTCTTTT[G/T]TTTTTAATAGCTATA | 9678 |
rs7810754 | snp | A/T | 0.5 | 0.000399361 | intron-variant | PHF14 | GRCh38.p7 | 7:11168442 | GGTTTGCTTTTACTT[A/T]ATAAAGTCAATTCAC | 9678 |
rs7810768 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961135 | tgcttttggtgtttt[A/G]gtcatgaagtctttg | 9678 |
rs7811275 | snp | C/T | 0.163892 | 0.234703 | intron-variant | PHF14 | GRCh38.p7 | 7:11114206 | TTGAAATTTTGACTC[C/T]CTATTTGTTTTGCCT | 9678 |
rs7811637 | snp | C/T | 0.105214 | 0.203807 | intron-variant | PHF14 | GRCh38.p7 | 7:11164994 | cagtggcgcgatctc[C/T]gctcactgcagcctc | 9678 |
rs7811934 | snp | G/T | 0.491732 | 0.0637633 | intron-variant | PHF14 | GRCh38.p7 | 7:11128385 | AAGTCTTTGTTATTT[G/T]CCCTACTTCATTCTA | 9678 |
rs8180695 | snp | G/T | 0.44546 | 0.155869 | intron-variant | PHF14 | GRCh38.p7 | 7:11058615 | CTATAGTGCCAGTTT[G/T]AATTTACTCTTTATT | 9678 |
rs9639070 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11002835 | ATGACAAAAATTAAC[A/G]GTGTGAGCACCAATA | 9678 |
rs9639071 | snp | C/T | 0.495927 | 0.0449436 | intron-variant | PHF14 | GRCh38.p7 | 7:11016538 | TTATGGAGAGTAAGA[C/T]TTATAAACCTGACTG | 9678 |
rs9647952 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10980508 | GGGTTTAATTGCTGT[G/T]AGTGGTTTACAAAAT | 9678 |
rs9768601 | snp | A/G | 0.497473 | 0.0354532 | intron-variant | PHF14 | GRCh38.p7 | 7:11077571 | GCGCCACTGCACTCC[A/G]GCCTGGCAACAGAGC | 9678 |
rs9969156 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11151887 | AATGACAGAATTTTA[C/T]GTTCCTCAGAAGCTG | 9678 |
rs9986755 | snp | C/G | 0.437683 | 0.165152 | intron-variant | PHF14 | GRCh38.p7 | 7:11037637 | ATGTACCTCTTCATC[C/G]TAATGAGAAAAGATT | 9678 |
rs10085512 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | PHF14 | GRCh38.p7 | 7:11108589 | AATGAAGGAATCAAT[C/T]AGCAAGGATTAGGTC | 9678 |
rs10085765 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PHF14 | GRCh38.p7 | 7:10976887 | CCCCTGGGGAGCTTA[A/G]ATTTGTGATCTGTGG | 9678 |
rs10215147 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:11026738 | ttttttttttttttt[A/T]aaatttaatttatta | 9678 |
rs10226402 | snp | C/G | 0.030665 | 0.119967 | intron-variant | PHF14 | GRCh38.p7 | 7:11023774 | tggaggttgcagtga[C/G]ctgagattgcgccac | 9678 |
rs10226792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11166625 | TTATGATAAAATCTA[C/T]TACTGTTATTTTGAT | 9678 |
rs10226931 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | PHF14 | GRCh38.p7 | 7:11112277 | AGCCATCTTTCTTCA[A/G]TGCTACTTAAATGAT | 9678 |
rs10227124 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:10994205 | gcactttgggaggcc[A/G]aggcagtgaatcact | 9678 |
rs10227195 | snp | C/T | 0.167484 | 0.23599 | intron-variant | PHF14 | GRCh38.p7 | 7:11075061 | tcctgcctcagcctc[C/T]tgagtagctgggact | 9678 |
rs10228209 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11034874 | TTTTTATCCTCAGTA[A/G]AATCTGTCCATTGTT | 9678 |
rs10228877 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | PHF14 | GRCh38.p7 | 7:11091449 | AGAAAGCATTTAAAA[C/T]TATGGGATTATAAAT | 9678 |
rs10228897 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | PHF14 | GRCh38.p7 | 7:11151674 | TTAAGACTCTTGAGT[G/T]TGAGCTATCAATGTT | 9678 |
rs10229335 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | PHF14 | GRCh38.p7 | 7:11020834 | AGAAGCTTTTAGGCT[C/T]TTTTTTCCTTGTAGT | 9678 |
rs10230399 | snp | A/G | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10970467 | cccagttaccaggga[A/G]gctgaggcaggagaa | 9678 |
rs10230966 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960139 | gtacatgtacacaac[A/G]tgcaggtttgttaca | 9678 |
rs10231002 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960325 | aactcccacttatga[C/T]tgagaacaggtggtg | 9678 |
rs10231114 | snp | A/G | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:11018258 | ttccgtatacatttt[A/G]ggattattttttcta | 9678 |
rs10231732 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11076447 | tttaaaatGTACTGT[C/T]TGCTTTTTAACTTTA | 9678 |
rs10232287 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11005930 | cctgagtagctggga[C/G/T]tacaggcatgcgcca | 9678 |
rs10233382 | snp | C/T | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10970772 | caaaatactagcaaa[C/T]tgaatctagcatcta | 9678 |
rs10235431 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961547 | ttaggattgtcttgg[A/C]tatgcgggctgtttt | 9678 |
rs10235587 | snp | C/T | 0.0349115 | 0.127424 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107253 | GCTTGTTATATGGAT[C/T]ATAGCACATATGAAG | 9678 |
rs10235649 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961558 | ttggctatgcgggct[C/G]tttttggtgccatat | 9678 |
rs10236024 | snp | A/G | 0.436265 | 0.166749 | intron-variant | PHF14 | GRCh38.p7 | 7:11043970 | GCTCTGGTTTCCAGC[A/G]TGTGAGAGTTTCTGC | 9678 |
rs10237668 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PHF14 | GRCh38.p7 | 7:11052939 | ttttaaataaaagtt[C/T]ggtgtgtatgttttc | 9678 |
rs10238096 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | PHF14 | GRCh38.p7 | 7:11168793 | GTTACCATTTAATAC[C/T]GAACACAAGATGCAC | 9678 |
rs10238895 | snp | A/G | 0.182296 | 0.240658 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965601 | accactgctctcttc[A/G]gagctgtcaggcagg | 9678 |
rs10240831 | snp | A/T | 0.172028 | 0.23753 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065825 | TGTGGCACATTTATT[A/T]CTTAATCAGAGATAG | 9678 |
rs10242027 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PHF14 | GRCh38.p7 | 7:11003016 | cagtggcatgatctc[C/T]gctcactgtcgcctc | 9678 |
rs10242037 | snp | C/G | 0.0271762 | 0.113356 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972956 | ctccctttgcaaacc[C/G]ccactttttctgcag | 9678 |
rs10242109 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | PHF14 | GRCh38.p7 | 7:11134730 | GCACTTCAGAAATTA[A/T]CGTAATCTTGTCATT | 9678 |
rs10242279 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | PHF14 | GRCh38.p7 | 7:11056294 | ATAGGTGGAGCTTTC[A/G]AGACTTTCCTTATTT | 9678 |
rs10242539 | snp | C/T | 0.0748431 | 0.178382 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973313 | gagggtatttggact[C/T]aagattctgtatccg | 9678 |
rs10242862 | snp | C/T | 0.0685596 | 0.171987 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105230 | ATTATATTTATGCAT[C/T]GTTTATAGATCATTG | 9678 |
rs10243749 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963356 | cagtagtcattcagg[A/G]gcaagttgttcagtc | 9678 |
rs10243910 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963644 | ttgttaattttctgt[C/G]tccttgatctgttta | 9678 |
rs10245045 | snp | A/G | 0.49917 | 0.0203505 | intron-variant | PHF14 | GRCh38.p7 | 7:11164189 | GGATGTTTGCCTGCT[A/G]TGAAGAACATATTTG | 9678 |
rs10245957 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | PHF14 | GRCh38.p7 | 7:11000657 | tttaccttttgtata[G/T]cttcttggatgaggt | 9678 |
rs10246591 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | PHF14 | GRCh38.p7 | 7:11114860 | AGCCACCCAGACAGT[A/G]CACTATGCTTATATT | 9678 |
rs10247314 | snp | A/C | 0.030665 | 0.119967 | intron-variant | PHF14 | GRCh38.p7 | 7:11021898 | TGCACCACAAAAACC[A/C]GAACCATGTAGCATG | 9678 |
rs10248811 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | PHF14 | GRCh38.p7 | 7:11009716 | GGCAGGTAAAAGTGG[C/T]AAGTAAAGAACTCTA | 9678 |
rs10248983 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | PHF14 | GRCh38.p7 | 7:11000758 | tgtatattttggata[A/T]cagttctttatcaga | 9678 |
rs10249565 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | PHF14 | GRCh38.p7 | 7:11098260 | CAGAATATTTTGGGA[A/G]CAGTTTTCTATTAAA | 9678 |
rs10250433 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961080 | agaagttctttagtt[C/T]aattatatcccattt | 9678 |
rs10250744 | snp | C/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11116039 | ctggggaagaacctt[C/G]agactatgtaaaaat | 9678 |
rs10251095 | snp | C/T | 0.449345 | 0.150869 | intron-variant | PHF14 | GRCh38.p7 | 7:11116321 | ccttttagtggaaaa[C/T]gatatttagaaacca | 9678 |
rs10251185 | snp | A/G | 0.454784 | 0.1434 | intron-variant | PHF14 | GRCh38.p7 | 7:11116202 | ttttgacatgattcc[A/G]ccaatcttcaggtac | 9678 |
rs10251254 | snp | C/G | 0.0715223 | 0.175059 | intron-variant | PHF14 | GRCh38.p7 | 7:11086378 | GGTCATTTTTTCTTT[C/G]TAAAACTAACCTGTT | 9678 |
rs10251314 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | PHF14 | GRCh38.p7 | 7:11052898 | ttaccaggtaccttg[A/G]aggggcctctaccaa | 9678 |
rs10252209 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | PHF14 | GRCh38.p7 | 7:11141113 | ACATTTCCTCATCAG[A/G]GAATGAATTGGTTCT | 9678 |
rs10253250 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | PHF14 | GRCh38.p7 | 7:11098913 | GTCTTTAGACTTAAA[A/G]TGATGCTTCATTGTA | 9678 |
rs10255050 | snp | C/T | 0.104504 | 0.2033 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962466 | agcttttcaatgtgc[C/T]gctggattcagtttg | 9678 |
rs10255688 | snp | C/T | 0.477175 | 0.104362 | intron-variant | PHF14 | GRCh38.p7 | 7:11111729 | ACATATTAAATAGTG[C/T]TCCGAAAGCCCAAAC | 9678 |
rs10256300 | snp | A/G | 0.173965 | 0.238157 | intron-variant | PHF14 | GRCh38.p7 | 7:11024478 | ccatagctagagagg[A/G]gaagtcactatctgg | 9678 |
rs10257220 | snp | A/G/T | 0.1586 | 0.237416 | intron-variant | PHF14 | GRCh38.p7 | 7:11011711 | ATTATATATGCTTTA[A/G/T]ATTGTTTCTTTGAAG | 9678 |
rs10257302 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972746 | GTAGGTTATACATTT[C/T]GGAATAGAAGTTTCT | 9678 |
rs10257578 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHF14 | GRCh38.p7 | 7:11042168 | aaaaCGCAAAATTCA[A/G]TATTGAAAAGAGACT | 9678 |
rs10258521 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962976 | tccctcttttcttct[C/T]tattaatcttgctag | 9678 |
rs10258657 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963078 | tttgtgtctctatct[C/T]cttcagttctgctct | 9678 |
rs10259271 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | PHF14 | GRCh38.p7 | 7:11088164 | acctatgcatatgtt[C/T]ctgtatgctttcagt | 9678 |
rs10259691 | snp | A/G | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10970627 | AGAGTAATTTATCAC[A/G]TACGCCTTAAAGATG | 9678 |
rs10261168 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PHF14 | GRCh38.p7 | 7:11018561 | attcactgttgtcac[A/G]tagacatgctcctga | 9678 |
rs10262117 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PHF14 | GRCh38.p7 | 7:10976206 | TTACTAATTGAATTC[A/G]TCCGCAGCAATCAAA | 9678 |
rs10263081 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | PHF14 | GRCh38.p7 | 7:11031291 | GTATAGCCTTCTGAC[A/G]TAGTCCTTTATCTCA | 9678 |
rs10263193 | snp | A/G | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:11001244 | tcagtttgttcatca[A/G]ctgacctatatatct | 9678 |
rs10263323 | snp | A/G | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:11001302 | gattactgcagcttc[A/G]tagtaagtcttgaag | 9678 |
rs10263407 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015013 | ATATAAGAGGGGGGG[G/T]GGGTACTTAAATTTT | 9678 |
rs10263654 | snp | G/T | 0.175576 | 0.238665 | intron-variant | PHF14 | GRCh38.p7 | 7:10985118 | TTTTAATTAAAAAAC[G/T]AATCAATTGTGATTA | 9678 |
rs10263908 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | PHF14 | GRCh38.p7 | 7:11015423 | AAAATATATAACAAA[C/T]GATTTGATGTATTGA | 9678 |
rs10266525 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | PHF14 | GRCh38.p7 | 7:11125372 | CTTTGTGTACACTGG[C/T]AGTTTTTGTATGTTT | 9678 |
rs10267002 | snp | A/G | 0.176219 | 0.238865 | intron-variant | PHF14 | GRCh38.p7 | 7:11001954 | agcttctagtttctc[A/G]tcgttaagtatgatg | 9678 |
rs10267151 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | PHF14 | GRCh38.p7 | 7:10994715 | gtccggagtttgctc[C/T]ttctgatgttcggat | 9678 |
rs10267293 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF14 | GRCh38.p7 | 7:11024921 | ataaggctatagctg[C/T]catacatagtgattc | 9678 |
rs10268993 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | PHF14 | GRCh38.p7 | 7:11020240 | gttataggtgtgcgc[C/T]accacaccaggctaa | 9678 |
rs10269354 | snp | C/G | 0.16846 | 0.236329 | intron-variant | PHF14 | GRCh38.p7 | 7:11020501 | ctcctacctcagcct[C/G]ccaagtagctgggac | 9678 |
rs10269690 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | PHF14 | GRCh38.p7 | 7:11020657 | gtgctgggattacag[G/T]catgagccactgtgc | 9678 |
rs10270849 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | PHF14 | GRCh38.p7 | 7:11156507 | AGTTTTAGAAATTCA[C/G]TTTCTggccgggcgt | 9678 |
rs10270986 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11096458 | TTAGGATGTTCTTAT[C/T]GTAAAGTTTTTGAAT | 9678 |
rs10270989 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126555 | AAATAAACTTTCTCT[C/T]TTCGTTATTTAGCTG | 9678 |
rs10272375 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962982 | ttttcttctttatta[A/G]tcttgctagcagtct | 9678 |
rs10273275 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963668 | ctgtttaatattgac[A/G]gtgcggtgttaaagt | 9678 |
rs10273598 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991487 | gccaatttttgtgtt[C/T]ttagtagagatgggg | 9678 |
rs10273828 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10991620 | tggtcCCCCAGTCat[C/T]ttaattaaaaaaaaa | 9678 |
rs10274322 | snp | A/C | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11096738 | GCCATTCAAAAAGAA[A/C]TCAAGATAATCTTCC | 9678 |
rs10276348 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967023 | tccattcattacagt[A/G]tcttcaacaaggcag | 9678 |
rs10276516 | snp | A/G | 0.444 | 0.157683 | intron-variant | PHF14 | GRCh38.p7 | 7:11122443 | CGTATATATATATAC[A/G]TATATATATATATTG | 9678 |
rs10276786 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967592 | tcacacctgtacccc[C/T]agcactttgagaggc | 9678 |
rs10276899 | snp | A/C | 0.030665 | 0.119967 | intron-variant | PHF14 | GRCh38.p7 | 7:11021897 | ATGCACCACAAAAAC[A/C]AGAACCATGTAGCAT | 9678 |
rs10277283 | snp | A/T | 0.0726307 | 0.176182 | intron-variant | PHF14 | GRCh38.p7 | 7:11013019 | AATTAGATCAAAGAC[A/T]TTTTGGTTTGTATCT | 9678 |
rs10277295 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | PHF14 | GRCh38.p7 | 7:11013049 | TTTGTTTTGCATGAG[C/T]TTGATCTTTTATATA | 9678 |
rs10277767 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957587 | AACATGAGTAAATAC[C/T]TCAGCTTGTCTAGGA | 9678 |
rs10277845 | snp | A/C | 0.180383 | 0.240111 | intron-variant | PHF14 | GRCh38.p7 | 7:10985339 | TTTTACTTTGTTTTC[A/C]GAAACTACTTTGTAG | 9678 |
rs10279430 | snp | A/G | 0.15698 | 0.23205 | intron-variant | PHF14 | GRCh38.p7 | 7:11158566 | TTTTAAATCATTTGA[A/G]TTTGGAAGACAGCTT | 9678 |
rs10279863 | snp | A/G | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:11085787 | tagtcttcaactcct[A/G]ggttcagtccttcca | 9678 |
rs10280227 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | PHF14 | GRCh38.p7 | 7:11058133 | GCTAAAGTAGTTTCA[A/G]CCTCAAAATATATCA | 9678 |
rs10280736 | snp | G/T | 0.0865458 | 0.189163 | intron-variant | PHF14 | GRCh38.p7 | 7:11084442 | ATATTCAGGGCCTAC[G/T]GGTGGCCTCCTCTTT | 9678 |
rs10281259 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958069 | gctgttataaaaaCT[C/G]AGCCCTGAGCCAATC | 9678 |
rs10281970 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958499 | tgacttttctttctg[C/G]gagtacttatgattt | 9678 |
rs10282681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11149877 | TTACAATTTTTATAC[G/T]TCATATCTTTCTCTT | 9678 |
rs10464254 | snp | A/G | 0.273049 | 0.248935 | intron-variant | PHF14 | GRCh38.p7 | 7:10975845 | TTGCCGTGGTTAGTC[A/G]CATCTCTCCTTCTTC | 9678 |
rs10464255 | snp | C/T | 0.272511 | 0.248984 | intron-variant | PHF14 | GRCh38.p7 | 7:10976853 | CTAGTATGCTGCACT[C/T]ATAATTTACCTTCCT | 9678 |
rs10486108 | snp | C/G | 0.303938 | 0.244112 | intron-variant | PHF14 | GRCh38.p7 | 7:10981023 | GATTTCATAGGGTCA[C/G]TCAGTATCTGTTAAA | 9678 |
rs10487898 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11054952 | TACGTATGTCATGAA[G/T]GTAAAATTTTCTTCA | 9678 |
rs10499379 | snp | A/T | 0.255658 | 0.252459 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149755 | CTGATGATTTTCCTC[A/T]TGAATGAATAGAGAT | 9678 |
rs10499381 | snp | A/G | 0.435407 | 0.167703 | intron-variant | PHF14 | GRCh38.p7 | 7:11152107 | TTGAAAATTGCTTTT[A/G]ATCAGTACTGCAAGA | 9678 |
rs10499382 | snp | A/T | 0.159292 | 0.232964 | intron-variant | PHF14 | GRCh38.p7 | 7:11152133 | CAAGATAGACTTAGG[A/T]CCTTTTAAGATAACT | 9678 |
rs10593375 | in-del | -/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153949 | CCTGTCTGTGTGTGC[-/GT]GTGTGTGTGTGTGTG | 9678 |
rs10625363 | in-del | -/GCACAC | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11088421 | CACACACACACGCAC[-/GCACAC]ACACACACACAGTCC | 9678 |
rs10658162 | in-del | -/A | 0.159951 | 0.233219 | intron-variant | PHF14 | GRCh38.p7 | 7:11077599 | GCGAGACTCTGTCTT[-/A]AAAAAAAAAAAAAAA | 9678 |
rs10659513 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068350 | CGAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 9678 |
rs10668180 | in-del | -/TT | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11127256 | TCCTTTTTTTTTTTT[-/TT]GACTCATTGCTAGAG | 9678 |
rs10669998 | in-del | -/AATT | 0.48498 | 0.0853497 | intron-variant | PHF14 | GRCh38.p7 | 7:11141890 | TCTGTCACAATTGAA[-/AATT]AATACTGCTTCTGTG | 9678 |
rs10693452 | in-del | -/A | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11157401 | ACCAAAAAAAAAAAA[-/A]TAGGTGTTGATTGCC | 9678 |
rs10713943 | in-del | -/T | 0.491885 | 0.0631791 | intron-variant | PHF14 | GRCh38.p7 | 7:11120050 | AAGTGATAATAGTTA[-/T]TTTTTCCCAAAAAAT | 9678 |
rs10807748 | snp | G/T | 0.472803 | 0.113397 | intron-variant | PHF14 | GRCh38.p7 | 7:11138183 | GTAGCTGGGATTACA[G/T]GTGCTCGCCACCACA | 9678 |
rs10950334 | snp | A/G | 0.492484 | 0.0608394 | intron-variant | PHF14 | GRCh38.p7 | 7:11124139 | AATATTGTAAAAGTA[A/G]TAAATGGTCATTGTT | 9678 |
rs11291559 | in-del | -/T | 0.488118 | 0.0761554 | intron-variant | PHF14 | GRCh38.p7 | 7:11084496 | GGGTTTACTCTTGTG[-/T]TTTTTTTTTTTTTTA | 9678 |
rs11323530 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047029 | AATCCTTTTTTTTTT[-/T]AACTTACACGAATAA | 9678 |
rs11342926 | in-del | -/A | 0.499992 | 0.00199679 | intron-variant | PHF14 | GRCh38.p7 | 7:11049475 | GCAAGACTGTCTCTC[-/A]AAAAAAAAAAAAAAA | 9678 |
rs11344507 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11156539 | GTGGCTCATGCCTGT[-/A]ATCTCAGCACTGTGG | 9678 |
rs11358931 | in-del | -/T | 0.16846 | 0.236329 | intron-variant | PHF14 | GRCh38.p7 | 7:11038993 | CCTTTGGGATAATGA[-/T]TTTCTGCTTGAAATA | 9678 |
rs11369981 | in-del | -/A | 0.486067 | 0.0822953 | intron-variant | PHF14 | GRCh38.p7 | 7:11157389 | TGTCAATGGGTTACC[-/A]AAAAAAAAAAAATAG | 9678 |
rs11384468 | in-del | -/A | 0.43655 | 0.16643 | intron-variant | PHF14 | GRCh38.p7 | 7:11057876 | CTAAATCAAGTTCTT[-/A]AAAAAAAAGAAAAAC | 9678 |
rs11390328 | in-del | -/A | 0.419936 | 0.183362 | intron-variant | PHF14 | GRCh38.p7 | 7:11110671 | AAGAAAGTGACAGGT[-/A]AATTTGTGAGAATAA | 9678 |
rs11404960 | in-del | -/A | 0.492484 | 0.0608394 | intron-variant | PHF14 | GRCh38.p7 | 7:11092559 | ACTCTTGAAGATTCC[-/A]AATCAGTAGGTGAAC | 9678 |
rs11486775 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11131884 | TCCATATGGTCCAGC[A/T]CTATTTGTTAATATT | 9678 |
rs11520738 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PHF14 | GRCh38.p7 | 7:11024378 | GATTTAGCTAAGACA[A/G]ATGATGAAGATTTGT | 9678 |
rs11520739 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11057397 | tttatttttttgaga[C/T]agagtcttgctctgt | 9678 |
rs11543619 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11089089 | GACACAAAGATTAAT[A/T]AGATATAAAAAAAAA | 9678 |
rs11549287 | snp | A/G | | | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022928 | TGGAGATATTGACAA[A/G]TTACGACCAGTAACA | 9678 |
rs11560245 | snp | C/G | 0.489608 | 0.0713316 | intron-variant | PHF14 | GRCh38.p7 | 7:11122703 | GTTAACACGTTTCTC[C/G]TTGGCAAAATGCCAT | 9678 |
rs11762175 | snp | A/C | 0.404907 | 0.196224 | intron-variant | PHF14 | GRCh38.p7 | 7:10975931 | ATATTACTGTTGCTA[A/C]TTTTAGTAGCATCAA | 9678 |
rs11762800 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PHF14 | GRCh38.p7 | 7:11019140 | attcggtttgctggt[A/G]ttttgttgaggatct | 9678 |
rs11762847 | snp | C/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107032 | TTAGCTTACAAATGG[C/G]TATAAATTATTTGCA | 9678 |
rs11767618 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11134845 | ACTATAGAAGGATAC[A/T]CAATGAATAATTCAG | 9678 |
rs11975710 | snp | A/G | 0.495671 | 0.0463237 | intron-variant | PHF14 | GRCh38.p7 | 7:11073712 | ttccgcactgcacta[A/G]tagaggctttctgtg | 9678 |
rs11976137 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11004225 | gcattccagtatggg[C/T]tacagaggaagactt | 9678 |
rs11977765 | snp | A/G | 0.478685 | 0.10101 | intron-variant | PHF14 | GRCh38.p7 | 7:11129542 | GCCTATTTTGTGTGT[A/G]TGTTTCTTTTTTTTT | 9678 |
rs11978011 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:10999284 | gtcctctctcaaacc[A/G]cttactcatttttgt | 9678 |
rs11978364 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987176 | AAATTGCTCTGAGTC[C/T]TAAAAAAAGGTTAGT | 9678 |
rs11978518 | snp | A/G | 0.497091 | 0.0380279 | intron-variant | PHF14 | GRCh38.p7 | 7:11129870 | TAAGGTACAGTGGGA[A/G]TTTTGAGAGTAGGAT | 9678 |
rs11979226 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | PHF14 | GRCh38.p7 | 7:11112750 | catgccaacctgggc[A/G]acagggcgagactcc | 9678 |
rs11979379 | snp | A/G | 0.298651 | 0.24522 | intron-variant | PHF14 | GRCh38.p7 | 7:10988004 | ctgggcaacaagagc[A/G]aaactccttctcaaa | 9678 |
rs11983086 | snp | C/T | 0.303438 | 0.244222 | intron-variant | PHF14 | GRCh38.p7 | 7:10988651 | CTTGCAACTTTTCTT[C/T]TGGGGGTACAAGGAA | 9678 |
rs12056132 | snp | A/C | 0.494526 | 0.0520291 | intron-variant | PHF14 | GRCh38.p7 | 7:11136506 | ACAAGTAAAAACTGA[A/C]TTACATTTTCCTTTT | 9678 |
rs12112182 | snp | C/T | 0.176219 | 0.238865 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968499 | TATTTAAATATTTAA[C/T]GATTCTTGGTTGTCT | 9678 |
rs12112329 | snp | C/T | 0.0402882 | 0.136092 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968838 | TCCATTCTGGTAATC[C/T]CTGAAGTTAGACTTC | 9678 |
rs12112341 | snp | G/T | 0.106278 | 0.204558 | | | GRCh38.p7 | 7:10969001 | TTCTCACAACCCTCA[G/T]TGTCTCTTACCTAAG | 9678 |
rs12112674 | snp | A/T | 0.445064 | 0.156365 | intron-variant | PHF14 | GRCh38.p7 | 7:11067904 | cccctgaggaggtca[A/T]taatctcttcatgaa | 9678 |
rs12112733 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11085720 | tgcaggtgtgtgcct[A/G]gctaatttttgtgtt | 9678 |
rs12154286 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075399 | gcatggcactagcat[C/T]tgcttctggcaaggc | 9678 |
rs12154295 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11075505 | aggaagcatcagatt[C/T]ttaactagcttttgt | 9678 |
rs12154349 | snp | C/T | 0.030665 | 0.119967 | | | GRCh38.p7 | 7:10970492 | ggagaatcacttgaa[C/T]ctgggaggcggaggt | 9678 |
rs12154647 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075587 | ttttttttttttttt[A/T]tttattattatgcca | 9678 |
rs12154735 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11034611 | tggagtgcagtggcg[C/T]gatctcggttaatta | 9678 |
rs12530833 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11059240 | GTTATTATCAAAATG[A/G]TAAATAAACATCCTT | 9678 |
rs12532164 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122352 | ATATATATATATATA[C/T]ACACACACACACACA | 9678 |
rs12534090 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975019 | GACTTTTTAAATCGG[G/T]TTTGATTAAAATGCC | 9678 |
rs12535184 | snp | C/T | 0.254664 | 0.249956 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960935 | ctttttgatgggttt[C/T]ttttttcttgtaaat | 9678 |
rs12537705 | snp | C/T | 0.288906 | 0.246954 | intron-variant | PHF14 | GRCh38.p7 | 7:10989129 | AGAAATACTAGAATT[C/T]TAAAGAGAAATGATA | 9678 |
rs12666244 | snp | A/G | 0.162909 | 0.23434 | | | GRCh38.p7 | 7:10969508 | TTGGATTTGGTTACC[A/G]TAATTTAGAATTATG | 9678 |
rs12666576 | snp | C/G | 0.093777 | 0.195178 | intron-variant | PHF14 | GRCh38.p7 | 7:11070137 | TGTTTGAGACAAGGT[C/G]TCATGATCACAGCTC | 9678 |
rs12667015 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | PHF14 | GRCh38.p7 | 7:11083535 | gtgcagtctcggctc[A/G]ctggaaactccgcct | 9678 |
rs12667160 | snp | C/T | 0.510468 | 0.0506746 | intron-variant | PHF14 | GRCh38.p7 | 7:11131130 | ggcagttatgaataa[C/T]gctactataaacatt | 9678 |
rs12669273 | snp | A/C | 0.2776 | 0.248472 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967037 | TGTCTTCAACAAGGC[A/C]GGTAGCTTCACCAAG | 9678 |
rs12669769 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | PHF14 | GRCh38.p7 | 7:11001514 | gacaatattgagctt[C/T]tttattcatgaacat | 9678 |
rs12669865 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967950 | ACTGGTAATCAAGAT[A/G]TCATTGCCTTTAAAT | 9678 |
rs12669876 | snp | A/G | 0.105569 | 0.204058 | intron-variant | PHF14 | GRCh38.p7 | 7:11153353 | gtttgtgtttgaaca[A/G]ctgagtcttatagac | 9678 |
rs12670220 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | PHF14 | GRCh38.p7 | 7:11016557 | TAAACCTGACTGTGG[A/G]AAATTTTTTGGCATG | 9678 |
rs12670880 | snp | A/T | 0.158302 | 0.232576 | intron-variant | PHF14 | GRCh38.p7 | 7:11160433 | ccagtaatgggattg[A/T]tggatctaatagtag | 9678 |
rs12671481 | snp | A/T | 0.170408 | 0.236992 | intron-variant | PHF14 | GRCh38.p7 | 7:11034013 | TGAAGTCCCATAGCC[A/T]GTAAATGATAGAGCC | 9678 |
rs12671644 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | PHF14 | GRCh38.p7 | 7:11030916 | TATTTCAAAACCCAG[A/G]ATATTGCATGAATCA | 9678 |
rs12672069 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11014163 | TGAGGCAGGTGGTAA[C/T]GTTTCTCATTTTATA | 9678 |
rs12672128 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11014442 | TGGAATGATGACCTC[C/T]TACCCTAGGTTGGGG | 9678 |
rs12673032 | snp | C/T | 0.121022 | 0.21416 | intron-variant | PHF14 | GRCh38.p7 | 7:11011734 | CTTTGAAGGATGTTT[C/T]ACATTAGGGCAGTGC | 9678 |
rs12674325 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11023449 | TATGTTATGTGTGTT[C/T]TGACTGCTTCACCAA | 9678 |
rs12699172 | snp | A/T | 0.469839 | 0.119042 | intron-variant | PHF14 | GRCh38.p7 | 7:11144923 | GACAGGGAGTAGAAT[A/T]ATGGTTGCTAGGAGG | 9678 |
rs13220950 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089759 | AGAATTGTTCATGCA[A/T]TCttttttttttttt | 9678 |
rs13220955 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089762 | ATTGTTCATGCAttc[C/T]ttttttttttttttt | 9678 |
rs13222436 | snp | C/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11059329 | TACATGATACATTTG[C/G]TAGTTCATTACCTAA | 9678 |
rs13223218 | snp | A/G | 0.00161681 | 0.0283865 | intron-variant | PHF14 | GRCh38.p7 | 7:11117621 | TACAAATATGTATTT[A/G]TATGTATAAATATGT | 9678 |
rs13223329 | snp | A/T | 0.0115144 | 0.0749975 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169789 | ACATTTAAATGACCT[A/T]AAAAAAAAACCTCTG | 9678 |
rs13224675 | snp | A/T | 0.494692 | 0.0512434 | intron-variant | PHF14 | GRCh38.p7 | 7:11069860 | attatttatttattt[A/T]tttttttCTGGTAGA | 9678 |
rs13226617 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11088414 | CACAAACACACACAC[A/G]CACGCACACACACAC | 9678 |
rs13227933 | snp | A/G | 0.495445 | 0.0475058 | intron-variant | PHF14 | GRCh38.p7 | 7:11113627 | CATTTTCCAATGAAA[A/G]ATGAAATTTAATATA | 9678 |
rs13227984 | snp | C/T | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106368 | AAATAGGTTCAAGCC[C/T]TCCACGTTAGTCTTA | 9678 |
rs13231972 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980414 | AACTCTGGttattat[G/T]tattaaatcataatt | 9678 |
rs13232272 | snp | C/T | 0.494815 | 0.0506538 | intron-variant | PHF14 | GRCh38.p7 | 7:11077683 | AGAACAGATATACCT[C/T]GTACATAGTCTCTTG | 9678 |
rs13234046 | snp | A/G | 0.310878 | 0.242475 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971985 | TTGTCACCCAGGCTG[A/G]AATGCAGTGGCGTGA | 9678 |
rs13234337 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002525 | ctcactgcaacctcc[A/C]cctcctgggttcaag | 9678 |
rs13234513 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972317 | GAAAATCTCCTTCTA[A/G]AAATTAGTTTTACAT | 9678 |
rs13236926 | snp | A/C | 0.494013 | 0.0543839 | intron-variant | PHF14 | GRCh38.p7 | 7:11126317 | ATTTTTACCACTTAA[A/C]ACAATTTTCAGAGTG | 9678 |
rs13237548 | snp | A/C | 0.0513262 | 0.151752 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972890 | ctaagaactaaattg[A/C]aaggaaacccctaac | 9678 |
rs13238824 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129701 | ATAGTATTCAGAAGG[G/T]GTGCCACATACTTCA | 9678 |
rs13238881 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075565 | tgggaaggaaagagg[G/T]ttttttttttttttt | 9678 |
rs13238887 | snp | C/T | 0.494143 | 0.0537956 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105668 | AATTAAGGATTGTGA[C/T]TTCTAAGATAGGCAT | 9678 |
rs13240677 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11000207 | CTACTACTTTCATCC[A/T]CTAGTTTAAATAATT | 9678 |
rs13240685 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11000238 | TCCCATTTCCCtttt[A/T]aattttggagtttct | 9678 |
rs13241115 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959762 | cccaaaacttggaga[C/T]gccagcaatggcaga | 9678 |
rs13241511 | snp | C/G | 0.438246 | 0.16451 | intron-variant | PHF14 | GRCh38.p7 | 7:11067653 | aagaaatacctgagg[C/G]tggataattgataaa | 9678 |
rs13241563 | snp | C/G | 0.00938946 | 0.0678717 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064342 | TTTATTACATTGCAT[C/G]TTAAATACTATCTTT | 9678 |
rs13241568 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004227 | attccagtatgggct[A/T]cagaggaagactttg | 9678 |
rs13241581 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004253 | ctttgtctcaaaaaa[A/G]aaaaaaaaaaaaaaa | 9678 |
rs13241669 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004211 | aagattgcaccactg[C/G]attccagtatgggct | 9678 |
rs13241687 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11004305 | TCTCATAATCATACC[A/T]CCTAGAGGTAAATAT | 9678 |
rs13242915 | snp | A/G | 0.383632 | 0.211288 | intron-variant | PHF14 | GRCh38.p7 | 7:11015005 | CCTCTCCAATATAAG[A/G]GGGGGGGTGGGTACT | 9678 |
rs13244792 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980504 | GGTTGGGTTTAATTG[C/G]TGTGAGTGGTTTACA | 9678 |
rs13245113 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11122921 | ACTTCTCTGAGCTGT[A/G]AATTCAGTTTGTCAA | 9678 |
rs13308126 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117582 | CCCAAACGATATATA[C/T]AAATATGTATTTATA | 9678 |
rs13309033 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030063 | CATATAGCTGTTCCA[A/G]TCTCTTCATTTATAT | 9678 |
rs13309058 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030070 | CTGTTCCAATCTCTT[C/G]ATTTATATAGCTGTT | 9678 |
rs13309487 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047970 | gggagggaggaaggg[A/C]AAAGAGAAAAACCTC | 9678 |
rs13309494 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047991 | GAAAAACCTCTTGGT[A/G]TTTCAACATGAAAGT | 9678 |
rs13309601 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047963 | agggagggggaggga[C/G]gaagggaAAAGAGAA | 9678 |
rs13311800 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162108 | ttttttttttttttg[A/G]gacagagccttgctc | 9678 |
rs13312211 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162106 | ttttttttttttttt[G/T]gagacagagccttgc | 9678 |
rs13438244 | snp | A/G | 0.0352966 | 0.128072 | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10958945 | TGGATTGCCAGGTTA[A/G]CTCTGCAAGGTAAGA | 9678 |
rs16876763 | snp | A/G | 0.174932 | 0.238463 | | | GRCh38.p7 | 7:10969759 | AGACAGGTTATTAAT[A/G]TTATTTCCAGATTCT | 9678 |
rs16876770 | snp | A/G | 0.191147 | 0.242974 | intron-variant | PHF14 | GRCh38.p7 | 7:10976854 | TAGTATGCTGCACTC[A/G]TAATTTACCTTCCTG | 9678 |
rs16876772 | snp | G/T | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:10988192 | ACATTTCTATTAAGA[G/T]CCTCAAGTCATGAGG | 9678 |
rs16876779 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11058686 | TCATTGGGCATCACA[A/G]TGTTACAGTTTAGTT | 9678 |
rs17149825 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | PHF14 | GRCh38.p7 | 7:10981062 | TTTATTTTTTATGCA[A/G]TTTTGCTTGCAGGAT | 9678 |
rs17149830 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | PHF14 | GRCh38.p7 | 7:10981114 | TATGTGACTTGTGGG[C/G]TTCACTAGATACCAG | 9678 |
rs17149834 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11059345 | TAGTTCATTACCTAA[A/G]AGATGAGTTGGATGA | 9678 |
rs17149838 | snp | G/T | 0.093777 | 0.195178 | intron-variant | PHF14 | GRCh38.p7 | 7:11061117 | GCTGTGATTGGTGGA[G/T]ATTTCTAACATATTG | 9678 |
rs17149839 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11140465 | TATATGAATGCAGTT[A/G]TAGAAGCAAATATGT | 9678 |
rs17163848 | snp | A/G | 0.271162 | 0.249103 | | | GRCh38.p7 | 7:10969632 | TTCTTTTTCTCTTAC[A/G]TCATTTTTTCATTGC | 9678 |
rs17163854 | snp | C/G | 0.0737376 | 0.17729 | intron-variant | PHF14 | GRCh38.p7 | 7:10974588 | AAGAGGGTCAGCTTC[C/G]ATTTTAGCTGGTCTG | 9678 |
rs17163856 | snp | A/C | 0.175576 | 0.238665 | intron-variant | PHF14 | GRCh38.p7 | 7:10978172 | AATCTGACTTTGAAT[A/C]AGTGGACCAAGATGT | 9678 |
rs17163857 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:10979001 | TTGATCTGTTATCTA[C/T]TGTGTATATTTATAG | 9678 |
rs17163862 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10980208 | TAATCTTACTTTTGC[A/G]TCTATCGTGAAGTTT | 9678 |
rs17163867 | snp | A/G | 0.175576 | 0.238665 | intron-variant | PHF14 | GRCh38.p7 | 7:10980471 | TGTTATTTTTACCAG[A/G]TGTGATTTTTCTTGG | 9678 |
rs17163872 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | PHF14 | GRCh38.p7 | 7:10983542 | CTTTCAACTTAGTTG[C/T]GTCCATATCCATATT | 9678 |
rs17163880 | snp | G/T | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:10987677 | ACCTATTTTCCTGAT[G/T]TCTATTTTTATGTAA | 9678 |
rs17163892 | snp | G/T | 0.117188 | 0.211804 | intron-variant | PHF14 | GRCh38.p7 | 7:10993371 | TTGCATGATCTGTGA[G/T]TCTCTAGCTAATGCT | 9678 |
rs17163893 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:10997044 | TAATGTATTCTGACT[C/T]TTTGGTGCCTTTTGC | 9678 |
rs17163894 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | PHF14 | GRCh38.p7 | 7:11000113 | AGTAATTTGAATTCT[A/G]TGAACTTTATATATG | 9678 |
rs17163895 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11002302 | TGCAATGTGGACGAT[A/G]TCATGCTGGAGCTTA | 9678 |
rs17163897 | snp | C/T | 0.103082 | 0.202275 | intron-variant | PHF14 | GRCh38.p7 | 7:11007830 | TAATTGCATAAGGAT[C/T]TTTAAGTTGAGATTT | 9678 |
rs17163898 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11009448 | AAATGGCCATAGAAA[C/T]ATGTCTTCTGTGTTA | 9678 |
rs17163903 | snp | C/G/T | 0.0652411 | 0.168531 | intron-variant | PHF14 | GRCh38.p7 | 7:11016125 | ATACTGTGGACGTTA[C/G/T]ATAAGTAGACACCTC | 9678 |
rs17163912 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11031259 | ATTGTGTACCTTTCT[C/G]TATTTTTTATGACTT | 9678 |
rs17163914 | snp | G/T | 0.0952156 | 0.196321 | intron-variant | PHF14 | GRCh38.p7 | 7:11032366 | TACCAGTAAAGCGTA[G/T]GTACGTTCTTCAAAT | 9678 |
rs17163915 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | PHF14 | GRCh38.p7 | 7:11035431 | CCCTTTAAAGAAAAA[A/C]GTTGTTGGTAATTTG | 9678 |
rs17163917 | snp | C/G | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:11045369 | CTTAGTCTGCAGCTT[C/G]AACTTCCACAGGTCC | 9678 |
rs17163919 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11048657 | TTCTTACCATCTTGT[G/T]TACCAATTAATGTAG | 9678 |
rs17163921 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | PHF14 | GRCh38.p7 | 7:11049885 | TAGGGGATAACCTGC[C/T]AGCTATATTTACATG | 9678 |
rs17163923 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | PHF14 | GRCh38.p7 | 7:11050263 | CTTGCTATGAGAATT[A/G]TAAGCTACATTCAAA | 9678 |
rs17163925 | snp | A/G | 0.159981 | 0.233231 | intron-variant | PHF14 | GRCh38.p7 | 7:11051573 | TAAAGCCAGAAGATA[A/G]TAATAAATGCATGAC | 9678 |
rs17163927 | snp | C/T | 0.0361523 | 0.129496 | intron-variant | PHF14 | GRCh38.p7 | 7:11051798 | AGTTTATTTTTTATT[C/T]ATCATAAGCATCATA | 9678 |
rs17163954 | snp | A/T | 0.108048 | 0.20579 | intron-variant | PHF14 | GRCh38.p7 | 7:11097453 | AAATTATGACTAGGG[A/T]TCACCATTAGGCGTA | 9678 |
rs17163958 | snp | C/G | 0.114036 | 0.209795 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106127 | TATGAATTGTTTTGT[C/G]TCATCTTTCATTTTC | 9678 |
rs17163959 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11110447 | TTGTTGTTAAATTTT[A/G]GTCTTGTTATTCCAA | 9678 |
rs17163973 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | PHF14 | GRCh38.p7 | 7:11133472 | TTTTCAGTTAATATA[C/T]TTTTAATGCAAAATG | 9678 |
rs17163974 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | PHF14 | GRCh38.p7 | 7:11133742 | TTATACATTTGGATT[A/T]TCCTCAACCACAAAC | 9678 |
rs17163995 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | PHF14 | GRCh38.p7 | 7:11138503 | TGTGCCCTGCGCACA[A/G]TTACCATACTACTAA | 9678 |
rs17163999 | snp | G/T | 0.0894459 | 0.191631 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149349 | ACAACTTAGGAGACA[G/T]AAATTCAGATTCTAA | 9678 |
rs17164002 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11155055 | TATGTCATTAATGAT[A/T]AAAAACTGTCGTAAA | 9678 |
rs17280846 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | PHF14 | GRCh38.p7 | 7:11062530 | TAATTAGCACTTTCT[C/T]ATTGCTTATCAAAAC | 9678 |
rs17346506 | snp | C/T | 0.495213 | 0.048687 | intron-variant | PHF14 | GRCh38.p7 | 7:11061168 | TACAGTTCTTTTAAA[C/T]GTTTGTATGCGTTCT | 9678 |
rs17347241 | snp | A/G | 0.494057 | 0.0541878 | intron-variant | PHF14 | GRCh38.p7 | 7:11096712 | CTGTTTGGATATATC[A/G]AGTTTTTATAGCCAT | 9678 |
rs17536100 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957101 | AGGCTTAGATTCAAG[A/G]TAATGACTACCCTTA | 9678 |
rs17536992 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | PHF14 | GRCh38.p7 | 7:10986997 | TTTTTTTTCCATAAA[A/T]GTCTCCGTTAAGTAC | 9678 |
rs28378773 | snp | A/T | 0.174288 | 0.23826 | intron-variant | PHF14 | GRCh38.p7 | 7:11080287 | TAAAAAAAACTTGAT[A/T]ACTTATATTACACGT | 9678 |
rs28384108 | snp | G/T | 0.0524604 | 0.153226 | intron-variant | PHF14 | GRCh38.p7 | 7:11167046 | AAATTTTTATTTCAT[G/T]TAACCATGTTCCAAT | 9678 |
rs28394821 | snp | A/C | 0.482309 | 0.0923707 | intron-variant | PHF14 | GRCh38.p7 | 7:11169362 | ATCTGTCAAGTATAG[A/C]TGATAAATGCTCTAA | 9678 |
rs28403972 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | PHF14 | GRCh38.p7 | 7:11128725 | CCACTGCTTTCCTCC[C/T]GTTCTCCTTCCGTCT | 9678 |
rs28414411 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | PHF14 | GRCh38.p7 | 7:11008355 | GGACAGGGGTCCCCA[A/C]CCAGGTGGTACTGGT | 9678 |
rs28420806 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | PHF14 | GRCh38.p7 | 7:11075344 | AATTTATAAAGAAAA[C/G]AGGTTTATTTGGCCC | 9678 |
rs28422022 | snp | C/T | 0.192401 | 0.243274 | intron-variant | PHF14 | GRCh38.p7 | 7:11008763 | TTTTTTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 9678 |
rs28444275 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | PHF14 | GRCh38.p7 | 7:11130031 | CCAAATTTTTAGTTG[A/T]TTAATATAAGTTGAT | 9678 |
rs28454079 | snp | A/G | 0.067446 | 0.170804 | intron-variant | PHF14 | GRCh38.p7 | 7:11006417 | GATGATCCCAATTTT[A/G]TTGGCAAGATTCAAA | 9678 |
rs28454278 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PHF14 | GRCh38.p7 | 7:10981663 | TATAGTAGTTACTGC[A/G]TAGAAGTTTTGAAAG | 9678 |
rs28458195 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090657 | TCTTGTTTTTCCCTT[A/T]AAAAATAAGATTCCT | 9678 |
rs28477426 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | PHF14 | GRCh38.p7 | 7:11166992 | TCTATATATATCTTA[C/T]CCATATATTTAAAAC | 9678 |
rs28489064 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | PHF14 | GRCh38.p7 | 7:10993088 | ACTGGTGATATTACT[A/G]TTACTTTTTTTCTCA | 9678 |
rs28492913 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | PHF14 | GRCh38.p7 | 7:11072389 | GTCCCATTTCCAACA[C/T]TGGGGACTATAATTC | 9678 |
rs28501468 | snp | A/C | 0.153332 | 0.230554 | intron-variant | PHF14 | GRCh38.p7 | 7:11145343 | GCTCTAGGAGGAAAA[A/C]CAGTTCTTCCTAGAA | 9678 |
rs28510200 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | PHF14 | GRCh38.p7 | 7:11115711 | CATTTATGGCAAAAG[A/G]ATTCGGTATAGAATC | 9678 |
rs28541920 | snp | C/G | 0.067446 | 0.170804 | intron-variant | PHF14 | GRCh38.p7 | 7:11006425 | CAATTTTGTTGGCAA[C/G]ATTCAAAGCATTGTA | 9678 |
rs28542277 | snp | C/T | 0.174288 | 0.23826 | | | GRCh38.p7 | 7:10970291 | TTTTCTGAGTTAAGG[C/T]TGGGTGCAGTGGCTC | 9678 |
rs28563906 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957820 | TTCATTTAAATGAAA[C/T]ATCTACAATACGAAA | 9678 |
rs28630530 | snp | A/T | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10971466 | AAAGGAATTAGGTAA[A/T]TTTTTTCTTTTCTTT | 9678 |
rs28631230 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11061767 | GGATTTTTGTTTTTT[G/T]TTTTTTTTTTTGTTT | 9678 |
rs28670953 | snp | G/T | 0.185155 | 0.241444 | intron-variant | PHF14 | GRCh38.p7 | 7:10993104 | TTACTTTTTTTCTCA[G/T]TTTTATTGCATAAGC | 9678 |
rs28682560 | snp | C/T | 0.173643 | 0.238054 | intron-variant | PHF14 | GRCh38.p7 | 7:10995031 | TTGACAGGGTGCTGA[C/T]TGGTGTGTTTACAAT | 9678 |
rs28682580 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | PHF14 | GRCh38.p7 | 7:11009014 | GTACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 9678 |
rs28693384 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | PHF14 | GRCh38.p7 | 7:11163710 | ACATTTTCATTATCG[C/T]CAGTATTTTCCAGTT | 9678 |
rs28698901 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122354 | ATATATATATATATA[C/T]ACACACACACACACA | 9678 |
rs28727326 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061776 | TTTTTTGTTTTTTTT[G/T]TTGTTTTTTTCCAGA | 9678 |
rs28756304 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | PHF14 | GRCh38.p7 | 7:11165549 | AAGAAATCTTTTAAA[C/G]TTGGCAGTCTACAAG | 9678 |
rs28776784 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988040 | AAAAAAAAGAAAAAG[A/G]AAAAAAAGAAAACTG | 9678 |
rs28802893 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961066 | TTCTTTTTCTGTGCA[A/G]AAGTTCTTTAGTTTA | 9678 |
rs28822717 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PHF14 | GRCh38.p7 | 7:11074414 | GCAGGGTTTCGCCGT[A/G]TTAGCCAGGATGGTC | 9678 |
rs28854787 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074208 | CCTTTCCTTTTTTTT[C/T]TTTTTTTCTTTTTTT | 9678 |
rs28876475 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074207 | GCCTTTCCTTTTTTT[C/T]CTTTTTTTCTTTTTT | 9678 |
rs28878781 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074215 | TTTTTTTTCTTTTTT[C/T]CTTTTTTTTTTTTGA | 9678 |
rs34002606 | in-del | -/A | 0.451483 | 0.148002 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149205 | CATCACAGTTGTTTT[-/A]AAAAGATGTATTCAT | 9678 |
rs34017542 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146067 | GACATTCTATTTTTT[-/G]GACAGTTTCTAGTGC | 9678 |
rs34033198 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047116 | TCTGTCACCCAGGCT[-/G]GGGGTGCAGTGGCAC | 9678 |
rs34033654 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046246 | CATTTGGTAGGATAC[-/A]AAATGGTAAGGGCTT | 9678 |
rs34067493 | in-del | -/T | | | | | GRCh38.p7 | 7:10969451 | TCTTCATTTATCTTA[-/T]TTTACTTTCCCTAAG | 9678 |
rs34070310 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004504 | CATTCAGGTACCATG[-/A]AGTTGCACTTGTGTT | 9678 |
rs34097352 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011613 | ATTTTGAGATGTAAT[-/A]AAATGTGTCTCAGGA | 9678 |
rs34149627 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993855 | CTCTGCTAAAAGTAC[-/A]AAAATTAATCCGGCA | 9678 |
rs34152096 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131942 | ACAATGGACTACTGG[-/A]AATTTTTTCTTGTTG | 9678 |
rs34166672 | snp | C/T | 0.497151 | 0.037632 | intron-variant | PHF14 | GRCh38.p7 | 7:11125561 | AGGAGTACAAAATTA[C/T]TACCTCACCTATAAA | 9678 |
rs34193754 | in-del | -/T/TTAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141892 | TGTCACAATTGAAAA[-/T/TTAA]TACTGCTTCTGTGAG | 9678 |
rs34238006 | in-del | -/T/TT/TTT | 0.499295 | 0.0187567 | intron-variant | PHF14 | GRCh38.p7 | 7:11127244 | GATTCTTGCCCCTCC[-/T/TT/TTT]TTTTTTTTTTTTGAC | 9678 |
rs34238815 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008255 | TTTTTTAGTGTATGC[-/A]AAAAGATATCCTTAG | 9678 |
rs34240680 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035111 | GATCGAAAATGTTTG[-/A]AAAAAAAAAAGCGTA | 9678 |
rs34295894 | snp | A/T | 0.497473 | 0.0354532 | intron-variant | PHF14 | GRCh38.p7 | 7:11078281 | ATCCTGCCTCTTTTC[A/T]GGGCAGTGATAGTGC | 9678 |
rs34307214 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998402 | AAACTGAATAAGGAA[-/C]ACATATACCTAAAAT | 9678 |
rs34309817 | in-del | -/AA | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11068349 | GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 9678 |
rs34327814 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005788 | TAGAAGTAAAAATTC[C/T]TTTTTTTTTTTTTTT | 9678 |
rs34351879 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134058 | GACTATCCAGTGCCT[-/G]GGGAAATTTTTCTTG | 9678 |
rs34353724 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156414 | AAACTGAAGATTAAT[-/G]GGGTTCACTCTGGGG | 9678 |
rs34355961 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000418 | ATCTTGGCTCACTGC[-/A]AACCTCTGTCTCCCA | 9678 |
rs34435801 | snp | A/G | 0.375 | 0.216506 | intron-variant | PHF14 | GRCh38.p7 | 7:10994803 | CTGCAGACCTTCGCG[A/G]TGAGTGTTACAGCTC | 9678 |
rs34478682 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11102113 | TTGCCATATTTGATG[-/A]AAAAAATAGCAAATT | 9678 |
rs34480920 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015006 | CTCTCCAATATAAGA[-/G]GGGGGGTGGGTACTT | 9678 |
rs34523531 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165358 | CGTTTTTAATACATC[-/G]GTATCAGGGTGTTAA | 9678 |
rs34540246 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147711 | CATTTGTGCTCAAGT[-/G]TGTATTAGTAACGCT | 9678 |
rs34579941 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049744 | CTTATCATTTCAATT[-/C]CTGAGATTCTGTAAG | 9678 |
rs34595247 | in-del | -/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956866 | TCAGATTTCTGACTT[-/C]CCAAAACTGTGAGAA | 9678 |
rs34635837 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092916 | GTGTTTTTTTCCCCC[-/T]TAATAGTGACCCTTG | 9678 |
rs34654248 | snp | A/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088500 | TGAAAATAACAGAGT[A/G/T]TTTTTGTTTTCATCC | 9678 |
rs34658159 | in-del | -/T/TT/TTT | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10988534 | TAGTTTCTAGTCTGT[-/T/TT/TTT]TTTTTTTTTTTTTTT | 9678 |
rs34658377 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11013418 | TGCCCACCTCGGCCT[-/C]CCCAAAGTGCTGGGA | 9678 |
rs34665460 | snp | C/T | 0.494272 | 0.053207 | intron-variant | PHF14 | GRCh38.p7 | 7:11133696 | GGGCAGTGTCCTTAC[C/T]GCACTTTTCATCTGC | 9678 |
rs34679172 | in-del | -/A | 0.440195 | 0.162252 | intron-variant | PHF14 | GRCh38.p7 | 7:11046645 | TGCTATTAAAGTTTT[-/A]TACAGGTATTATAAC | 9678 |
rs34686939 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069903 | ATTAGATAATACTGG[-/C]CCTTCTGAATGGAGT | 9678 |
rs34711475 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029599 | AAAAGTGTATACTTC[-/G]GGTAATGGACCCATT | 9678 |
rs34728306 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976454 | AACTTTGACAAACAT[-/A]AGTTGGGTCGTGGAA | 9678 |
rs34741581 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990506 | AATAAGAGGGTGCTT[-/C]ACAGGGTTCTTTGAT | 9678 |
rs34761667 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PHF14 | GRCh38.p7 | 7:11012973 | TTACAATTGTATTAT[A/G]CCTGTTTGTATTATA | 9678 |
rs34770071 | in-del | -/A/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031591 | GACCCCATCTCTACC[-/A/AA]AAAAAAAAAAAAAAA | 9678 |
rs34783802 | in-del | -/T | 0.480853 | 0.0959518 | intron-variant | PHF14 | GRCh38.p7 | 7:11138041 | TCTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTTG | 9678 |
rs34785076 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025945 | GGCAAAACCCTGTAT[C/T]TACTAAAAATACAAA | 9678 |
rs34802861 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122459 | TATATATATATATTG[G/T]GTGTGTGTGTGTGTC | 9678 |
rs34812487 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114866 | CAGACAGTGCACTAT[-/G]GCTTATATTCAGTGG | 9678 |
rs34817220 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015537 | CATTAAGTGTGCACC[-/T]TTCAAGTTGGACTGT | 9678 |
rs34828969 | in-del | -/A | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963748 | ACTTGCTTTATGAAT[-/A]CTGGGTGCTCCTGTA | 9678 |
rs34872517 | in-del | -/AG | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11015003 | TTCCTCTCCAATATA[-/AG]AGGGGGGGTGGGTAC | 9678 |
rs34914921 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073787 | TTCCTCTGAAACCTA[A/G]GTGGAGGCTGCCAAG | 9678 |
rs34933725 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:10982202 | TATCAACTTCATTGA[C/T]TTATTATTTGATCAG | 9678 |
rs34960792 | in-del | -/T/TTT | 0.478768 | 0.100824 | intron-variant | PHF14 | GRCh38.p7 | 7:11087197 | TCTTTCTTTTTTTTT[-/T/TTT]GTTAAGATGGAGTCT | 9678 |
rs34966429 | in-del | -/C | 0.494976 | 0.0498674 | intron-variant | PHF14 | GRCh38.p7 | 7:11048895 | ATTTTTTGAGTTGTT[-/C]CGTGTTTTGTGGTGT | 9678 |
rs34970312 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027723 | TTGTCTTAAAGATAT[-/T]TAAAACATGCATGAT | 9678 |
rs34970712 | in-del | -/T | 0.496416 | 0.0421803 | intron-variant | PHF14 | GRCh38.p7 | 7:11042977 | TAAATCTATAACAGC[-/T]TTTTTTGAGAAATGA | 9678 |
rs34990314 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126715 | CTAAGATAGCAATGT[-/C]CCCTAATAGGGTAAA | 9678 |
rs35048896 | in-del | -/AT/TATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027719 | TTAGTTGTCTTAAAG[-/AT/TATT]ATTTAAAACATGCAT | 9678 |
rs35071886 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011940 | AGAACTTTTCAATTT[-/C]CCATTTATCAGATTC | 9678 |
rs35101404 | in-del | -/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149811 | TAGTGTTTCAGTTGA[-/T]TTTTTTTTTATATTT | 9678 |
rs35118226 | in-del | -/A | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956553 | AATTCATGAACACCT[-/A]AGAACCTCAGAATGT | 9678 |
rs35132328 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092945 | GAATCAGATTGGCAT[-/G]GGCAACGTTCTAGAT | 9678 |
rs35228140 | snp | A/G | 0.428786 | 0.174744 | intron-variant | PHF14 | GRCh38.p7 | 7:11153965 | TGTGTGTGTGTGTGT[A/G]TGTGTGTTTTAAGAA | 9678 |
rs35250418 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162306 | TGCTGGCCAGGCTGG[G/T]CTCAAACTCCTGGCC | 9678 |
rs35265144 | snp | G/T | 0.47885 | 0.100637 | intron-variant | PHF14 | GRCh38.p7 | 7:11087207 | TCTTTCTTTTTTTTT[G/T]TTAAGATGGAGTCTC | 9678 |
rs35292828 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088830 | TAAAAAATTATGTAT[-/C]CTCCTATAGATTTAT | 9678 |
rs35327585 | in-del | -/A | 0.498206 | 0.0298983 | intron-variant | PHF14 | GRCh38.p7 | 7:11168019 | GAAAGAGTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 9678 |
rs35360978 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983976 | GTTTTTCTTCAAAAG[-/A]AAAGATTGAGTTGTT | 9678 |
rs35365137 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974068 | ACTGCGCTGCCTGGG[-/C]CCGGAGGTCTTCTCC | 9678 |
rs35419476 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135362 | CTGCACATGTCCACA[-/G]GGGAAAAGAAATGGT | 9678 |
rs35507980 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | PHF14 | GRCh38.p7 | 7:11068963 | ATGCATTTTTAAGAA[C/T]GTAATGTTTTTGATG | 9678 |
rs35558412 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997111 | TCTATCCCTTTCTGT[-/G]CTGTATTTAATGCAT | 9678 |
rs35580506 | snp | A/C | 0.497776 | 0.0332724 | intron-variant | PHF14 | GRCh38.p7 | 7:11067850 | GCCAGGCTCTTTTTA[A/C]TATCCAACTATCAAA | 9678 |
rs35594158 | snp | C/G | 0.495483 | 0.0473088 | intron-variant | PHF14 | GRCh38.p7 | 7:11078115 | TCTGACGAAAGAGAA[C/G]AGAAGCTATCTAACC | 9678 |
rs35619104 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101807 | TCATCTTCACAGATC[-/T]TAAATGTTTGAAGGA | 9678 |
rs35639676 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | PHF14 | GRCh38.p7 | 7:11000940 | AAGTCGTTACTATGC[C/G]TGAGGTTATCTAGAT | 9678 |
rs35639936 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148185 | TAATTTCTACCCATC[-/T]TTTCTCTATACCTCA | 9678 |
rs35648039 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | PHF14 | GRCh38.p7 | 7:11130094 | ACAGAGCAGCTCTGC[C/T]CATTATAGTCACTTG | 9678 |
rs35659048 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030654 | AGGAAATTTACAGGG[-/G]AAACAGATACATTAG | 9678 |
rs35671995 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149183 | CATGTAGATGTTTTA[A/G]GTAAGGCCATCACAG | 9678 |
rs35700406 | in-del | -/A/AA | 0.347253 | 0.230308 | intron-variant | PHF14 | GRCh38.p7 | 7:11009035 | GTGAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 9678 |
rs35703070 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016974 | GTTTGGTTTTTAGAT[-/C]CCCACAAATAAGTGA | 9678 |
rs35721912 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146072 | TCTATTTTTTGACAG[-/T]TTTCTAGTGCTGTAA | 9678 |
rs35754830 | snp | C/G | 0.304438 | 0.244001 | intron-variant | PHF14 | GRCh38.p7 | 7:11035314 | GATTTTGGTATCCTT[C/G]GGGGGTCCTGGAACC | 9678 |
rs35763725 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161629 | TAACATTTTTAAATA[-/T]TTATTTTTGCCTAAA | 9678 |
rs35765916 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061360 | TTTACATAAACATGT[-/A]ATGCACATGCATATA | 9678 |
rs35794160 | in-del | -/T | 0.134802 | 0.221877 | intron-variant | PHF14 | GRCh38.p7 | 7:11121855 | TGTTTATTTCTGGAA[-/T]TTTTTTTTTTCTATA | 9678 |
rs35830569 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026756 | TTTAATTTATTACAA[-/G]GGAATTTTTCTAAAT | 9678 |
rs35857511 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996701 | TTAACTCATTTAGGC[-/T]TGGGGTTTAAGTAGG | 9678 |
rs35858026 | in-del | -/ATA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072547 | AATAGTACCTACTCC[-/ATA]GATTGTCTGGATGAT | 9678 |
rs35888335 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111776 | CTTAACACACTTGAG[-/T]AATGGCAGGAAAATT | 9678 |
rs35934105 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049219 | GCTCACACCTGTAAT[-/C]CCCAGCACTTTGGAA | 9678 |
rs36030787 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120430 | TAACCTGAAGAGTAA[-/T]TTTTCTGTTTCATTT | 9678 |
rs36042390 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990871 | GCTTTCTTTTCTCTC[-/TT]TTTAGAAATGGCTGA | 9678 |
rs36053908 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138332 | GGCGTGAGCCACTGC[-/G]GCCTGGCCGGAAAAA | 9678 |
rs36061083 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039197 | TAGCAGTTTTAGATT[-/C]CCCTGCCACATTTTT | 9678 |
rs36074419 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120142 | TTAAATTATATAGAA[-/C]AGTTAAGTATGCAAT | 9678 |
rs36083343 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036499 | AGGCCTGGGTTCCAA[-/G]GGGAAAAATTGCCCA | 9678 |
rs36108941 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977915 | GACTTATTTACATTT[-/G]GGTTATCTGCTACAT | 9678 |
rs41272942 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11036887 | TTAAAAGTTTTAAAC[G/T]ATGTAGGTTTATCAA | 9678 |
rs41273045 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11040478 | TGATGAAAGTCTGTA[A/G]TTATAGATTTCTAAT | 9678 |
rs55704333 | snp | A/G/T | 0.0391387 | 0.134304 | intron-variant | PHF14 | GRCh38.p7 | 7:11023184 | TTAATTTAGAGTAAC[A/G/T]TATGAGGTAAAATGA | 9678 |
rs55765639 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11122386 | ACACACACACACACA[C/T]ACATACACACACATA | 9678 |
rs55776725 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11122390 | ACACACACACATACA[C/T]ACACACACATATATA | 9678 |
rs55801039 | in-del | -/ATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075589 | TTTTTTTTTTTTTTT[-/ATT]TATTATTATGCCATT | 9678 |
rs55813149 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | PHF14 | GRCh38.p7 | 7:11142719 | TTTTGCTTTAGTCAC[C/T]TGTTCACTATCCAAG | 9678 |
rs55824214 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004546 | GTCTCCATTAATCTA[A/G]AACAATTTTTCTGCC | 9678 |
rs55885944 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11075783 | AAATAAGTATTAATA[C/T]CTCCTTTGAATTGAT | 9678 |
rs55898701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027646 | AGAAAGAATGTACAT[A/T]ATTGACTGTGTTGTA | 9678 |
rs55900463 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PHF14 | GRCh38.p7 | 7:11027580 | TCTGAGAGGATTTGC[A/G]GTAATTTCAACAGTT | 9678 |
rs55917513 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004268 | AAAAAAAAAAAAAAA[-/AA]GAAAAGAAAAAGAAA | 9678 |
rs55954463 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004595 | TGTTGACATATTGAA[A/G]AATCTTAGTTTTTAT | 9678 |
rs55970254 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PHF14 | GRCh38.p7 | 7:11053491 | GGCTAGTTTCTATTT[C/T]TAAAATATTTTCTAT | 9678 |
rs55976132 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046989 | TGGATTTATTTATTG[C/G]ATTATTGCATTTAAA | 9678 |
rs55985150 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138779 | AATTGTATTTTCCTT[G/T]TTTTTACAATTTGAA | 9678 |
rs55993437 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11113162 | TAAATATACCTTTTT[A/G]CATATATTCTTTTGA | 9678 |
rs56043099 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034565 | TTTTTTTTTTTTTTT[-/TT]GAGACAGACTGTCGC | 9678 |
rs56071938 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11159932 | TTCAACTTTTATTTT[A/C]GATTCAAGAGGTACA | 9678 |
rs56096263 | snp | A/C/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11121459 | ACAGTAGCCTCCCCC[A/C/G]ACTGCCTACTTAATT | 9678 |
rs56164190 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031608 | AAAAAAAAAAAAAAA[-/AA]TTAGCTGGGTGTGAT | 9678 |
rs56208661 | snp | C/T | 0.0240643 | 0.107019 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066397 | CCCGAGTAGCTGAGA[C/T]TTGATTTTTTATTTT | 9678 |
rs56231729 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11116471 | TTGCTTTCATAGACA[C/T]TGAAAACTAATTTTC | 9678 |
rs56235368 | in-del | -/T | 0.485049 | 0.0851591 | intron-variant | PHF14 | GRCh38.p7 | 7:11004352 | TTTGTTCTTCCAGGC[-/T]TTTTTTTTTTTTTTG | 9678 |
rs56285844 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133489 | TTTAATGCAAAATGG[G/T]TGGGCATTAGATTGA | 9678 |
rs56317450 | snp | A/G | 0.300421 | 0.244863 | intron-variant | PHF14 | GRCh38.p7 | 7:11137720 | CCTCCCGATTAGGTG[A/G]GATTACAGGCACCTG | 9678 |
rs56335534 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11122430 | ATATATATATACACG[C/T]ATATATATATACGTA | 9678 |
rs56367816 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11016765 | TACCCTCTTTAAGTT[A/G]TTTTTAAGTGTACAA | 9678 |
rs56400834 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | PHF14 | GRCh38.p7 | 7:10995655 | ATGGCGGGGTGGGTA[A/C]GGCTCAGGCATGGTG | 9678 |
rs56680594 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141887 | CTTATCTGTCACAAT[G/T]GAAAATACTGCTTCT | 9678 |
rs56685525 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11056601 | GAAACAGATGACACC[G/T]TGTTCATAATTTGTT | 9678 |
rs56799320 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11041200 | AATGAAGATAAGTTT[C/T]AGTTTTGAGTTTCTA | 9678 |
rs56802892 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11108337 | TTGACTTCAAGATTG[G/T]ATTCTTTTCTTTTTT | 9678 |
rs56913090 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11109611 | AATTTTGGCTAATGA[A/G]AGGTAAATATGTTGT | 9678 |
rs57011556 | snp | A/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11041212 | TTTTAGTTTTGAGTT[A/T]CTACACTTTTTTTCT | 9678 |
rs57022517 | in-del | -/T | 0.0248432 | 0.108648 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102767 | TTTTCTTCTTTTTGC[-/T]TTTTTTTGCACTTAT | 9678 |
rs57101795 | snp | A/C | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:10970160 | TCTTCTTTGTGTAGT[A/C]ATGCATAAATATCTT | 9678 |
rs57172721 | in-del | -/TTTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075586 | TTTTTTTTTTTTTTT[-/TTTTT]ATTATTATGCCATTC | 9678 |
rs57184355 | in-del | -/AT | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11033015 | GGTAGAACCCACCTC[-/AT]GTGGTAGTGGTGAAG | 9678 |
rs57246905 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11059095 | AGAAATTTATAAATA[G/T]AGAGAGAAATGGAGC | 9678 |
rs57277658 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131831 | TACGTTCTCTCTCTG[-/TC]TCTCTCTCTCTCATT | 9678 |
rs57281048 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11054973 | GACATACGTAGGGCA[A/G]TCATGACATACCCCA | 9678 |
rs57327184 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | PHF14 | GRCh38.p7 | 7:11024882 | TTTTGACTTTAAAGT[C/G]TGATTATTTAAGAAA | 9678 |
rs57337126 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11112185 | ATGAAGACATTCTGG[G/T]CAACTGTAGATTAAT | 9678 |
rs57600747 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11034378 | CATCTTTACAAGTTG[C/T]TTTTGATAGAATAAA | 9678 |
rs57721336 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053069 | TCAAAAATCTTCCTT[-/T]CCACAAGGGAGATAC | 9678 |
rs57841461 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11136431 | AATAATATAATTACC[A/G]GAGTAAAGTATCTGT | 9678 |
rs57951445 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149633 | TACACTTGGTGGGCA[A/G]TATTCCTTTTAATCA | 9678 |
rs57982430 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11072504 | TTGCCTGTGTTTTAC[C/T]TTCATTATCTATAAA | 9678 |
rs58148239 | in-del | -/A | 0.0543475 | 0.155628 | intron-variant | PHF14 | GRCh38.p7 | 7:11046933 | TAAATTGTGGAGGAG[-/A]AAAAAGTAAATCATG | 9678 |
rs58175304 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990656 | GATTAAGTTTTTTTT[-/TT]ACTTTAAATGTGATT | 9678 |
rs58253114 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:11062289 | AATGTAAATAAGAGT[C/G]ATAATCTGCCTGTTT | 9678 |
rs58282147 | in-del | -/GTGTGT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041443 | TGTGTGTGTGTGTGT[-/GTGTGT]ATGTATGTGTGTGTA | 9678 |
rs58359719 | in-del | -/CAT | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11060914 | CAGTGTACTTGATAT[-/CAT]GAAGAATTGAAATTA | 9678 |
rs58380835 | in-del | -/AG | 0.0146672 | 0.084371 | intron-variant | PHF14 | GRCh38.p7 | 7:11093850 | TTCCTTCTGACTCTC[-/AG]GGGTAGGAGACCTTT | 9678 |
rs58442127 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11119406 | CAATATATCATAGAT[A/C]GTACTGTTATAAAAT | 9678 |
rs58496723 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143398 | AATGCTAGGATTATA[A/G]GCATGAGCCACCATG | 9678 |
rs58621951 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11143125 | TTGGCTTGATAATTG[A/G]CTTTTTCAACAATGG | 9678 |
rs58675172 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11132318 | TTTTTTTTTTTTTTT[-/T]AGATTCCACATAAAA | 9678 |
rs58700195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980173 | CAATTTTGATCAGCT[A/G]CCCACACTTCTGCCC | 9678 |
rs58710725 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | PHF14 | GRCh38.p7 | 7:11131727 | ATTTTCTACTATGTT[A/G]TCTTCTGGGAGTTTT | 9678 |
rs58711986 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10985673 | TTTTTTTTTTTTGGA[A/G]ACAGGGTCTCACTCT | 9678 |
rs58735396 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11072511 | TGTTTTACCTTCATT[A/G/T]TCTATAAAATAGCAA | 9678 |
rs58883350 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11043766 | ATTATGGTTTTTATG[C/T]GCTTCAGAAACTGCT | 9678 |
rs58903529 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PHF14 | GRCh38.p7 | 7:11083016 | TAGCTCTCTAGCTTA[C/T]CACAGATGACTTCTA | 9678 |
rs58927562 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PHF14 | GRCh38.p7 | 7:11034614 | AGTGCAGTGGCGCGA[C/T]CTCGGTTAATTACAA | 9678 |
rs58959421 | in-del | -/ACG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002459 | TTATTTATTTTTGAG[-/ACG]GAGTTTTGCTCTTGT | 9678 |
rs59102692 | snp | G/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11131511 | TGTAAAATTATTGTT[G/T]AATTTTAAAGAGTTA | 9678 |
rs59114503 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138778 | TAATTGTATTTTCCT[G/T]GTTTTTACAATTTGA | 9678 |
rs59328153 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11034658 | TATTCAAGCAATTCT[C/T]CTACCTCAGCCTCCT | 9678 |
rs59426929 | snp | G/T | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036617 | ACAATTCAGATACTA[G/T]TTCTAGTGTGGATGG | 9678 |
rs59434425 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11044136 | GAAGCTAAACACTGG[A/G]TAGTCATGGACATAA | 9678 |
rs59441504 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PHF14 | GRCh38.p7 | 7:11032650 | GATGGGGCATTCCAG[C/T]TTGCCACAGGCTCTA | 9678 |
rs59451704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134953 | TTGCACATAAACATG[C/G]TGATATCTTTGTCCT | 9678 |
rs59674198 | snp | A/G | 5.11391e-05 | 0.00505638 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102527 | CACAGCTCATCCTCG[A/G]AGGCAATCCCGGAAA | 9678 |
rs59702121 | in-del | -/A | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:11111908 | CCTTTAAAAAAAAAA[-/A]CAAAATAGTTTTCAT | 9678 |
rs59707181 | in-del | -/ATTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056403 | ATTAGACCCATAGTT[-/ATTT]CAGTTTATAGTAGTT | 9678 |
rs59779799 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988015 | GAGCGAAACTCCTTC[C/T]CAAAAAAAAAAAAAA | 9678 |
rs59807745 | snp | A/T | 0.00314647 | 0.039539 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035681 | TTGTAAGCAACATGC[A/T]GATAGGTTAGACAGA | 9678 |
rs59808302 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11088354 | TGCAGATATGGAGGG[A/C]AGACTGTATTAACTT | 9678 |
rs59953496 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162718 | TTTTTTTTTTTTTTT[-/T]GATATGGAGTTTCGG | 9678 |
rs59992534 | in-del | -/T | 0.407158 | 0.194426 | intron-variant | PHF14 | GRCh38.p7 | 7:10979450 | AATTTTAAAGATATA[-/T]TTTTTTCAAACGTAA | 9678 |
rs60123000 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046990 | GGATTTATTTATTGC[A/C]TTATTGCATTTAAAG | 9678 |
rs60185956 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:10976103 | GCAGTAACGGATCCA[A/G]TGGATTTGACTTCAG | 9678 |
rs60254068 | in-del | -/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153971 | TGTGTGTGTGTGTGT[-/GT]TTTAAGAATAAGGAA | 9678 |
rs60358801 | snp | A/C/T | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11025849 | GGGTGCGGTGGCTCA[A/C/T]GCCTGTAATCCCGAC | 9678 |
rs60415355 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141888 | TTATCTGTCACAATT[A/G]AAAATACTGCTTCTG | 9678 |
rs60418788 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11069823 | TTGGTATTACCACCA[C/T]ACCACCATGCCCAGC | 9678 |
rs60453852 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101920 | AGGTAACAAATAATT[C/G]TAACCAAACATATTT | 9678 |
rs60502036 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11019687 | CTTTTCAAAATACTA[A/G]CATTTTGTTTCATTG | 9678 |
rs60680874 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11020116 | TCCAATCAGACGGGG[C/T]CTGGCTCTGTTCCCC | 9678 |
rs60714759 | in-del | -/A/CAA | 0.483923 | 0.0882034 | intron-variant | PHF14 | GRCh38.p7 | 7:10988016 | GCGAAACTCCTTCTC[-/A/CAA]AAAAAAAAAAAAAAA | 9678 |
rs60946963 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11131743 | TCTTCTGGGAGTTTT[A/G]TAGTTTTGCATTTTA | 9678 |
rs60979082 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11046329 | ATGTTATATTTCTGC[C/T]TCCACTCATCTGATT | 9678 |
rs61011519 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11020112 | TTTTTCCAATCAGAC[A/G]GGGCCTGGCTCTGTT | 9678 |
rs61148452 | snp | C/T | 0.115088 | 0.210473 | intron-variant | PHF14 | GRCh38.p7 | 7:11162341 | ATGATCCACCCACCT[C/T]GGCCTTCCACAGTGC | 9678 |
rs61250143 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10985669 | TTTTTTTTTTTTTTT[-/T]GGAGACAGGGTCTCA | 9678 |
rs61302979 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:11049558 | AGAAATGATCAGTTA[A/G]CATTAAGATTACAAT | 9678 |
rs61481160 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149278 | ATCATTTAATCTAAA[A/G]TCATATTGACTCATT | 9678 |
rs61555147 | in-del | -/TT | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10988554 | TTTTTTTTTTTTTTT[-/TT]AACCTAGATGTGGTA | 9678 |
rs61639394 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11019685 | ACCTTTTCAAAATAC[C/T]AACATTTTGTTTCAT | 9678 |
rs61646663 | snp | A/G/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11034749 | AGACAGGCTTTTGCC[A/G/T]TGTTGGCCAGGCTAG | 9678 |
rs61647045 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11034769 | GGCCAGGCTAGTCTC[A/G]AACTCCCAACCTCAA | 9678 |
rs61665236 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009052 | AAAAAAAAAAAAAAA[-/A]GTCTTTTTTATTGAT | 9678 |
rs61698202 | in-del | -/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149819 | CAGTTGATTTTTTTT[-/T]ATATTTCTAAGTATA | 9678 |
rs61707274 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11147123 | AAAGTGCTGGGATTA[C/T]GGGCATAAGCCGCCA | 9678 |
rs61753124 | snp | C/G | 0.0386883 | 0.133594 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982933 | AGAGAAAAGGGAGAT[C/G]TGCGTCTCAGAAAGA | 9678 |
rs61753125 | snp | C/T | 0.0613193 | 0.164011 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042812 | GACCAAAAACAGTTA[C/T]TGGTGAGTAAAATAG | 9678 |
rs61996283 | snp | A/G | 0.0103865 | 0.0713118 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028812 | TTCAGAGGCAGCGGC[A/G]GAAGAGGTAGGTTTA | 9678 |
rs61996284 | snp | C/G | 7.41098e-05 | 0.00608682 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990737 | AGAGTCAAAACTGGA[C/G]CTCTCAAAAAATGGA | 9678 |
rs61996285 | snp | A/G | 0.00218891 | 0.03301 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051730 | GAACCAGTGAAATTT[A/G]TTCCACAGGATGTGC | 9678 |
rs62438452 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973654 | ATTAGGCGCGGAGAG[G/T]GCGGAGCCTTTGGGG | 9678 |
rs62438453 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992598 | AACCCAGGAGGTGGA[A/G]GTTGCAGTGAGCCGA | 9678 |
rs62438454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11005772 | CTGTGGGATAGATAC[C/T]TAGAAGTAAAAATTC | 9678 |
rs62438681 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137649 | TGCCCAGGCTAGAGT[A/G]CAATGGCACAATCTC | 9678 |
rs62438683 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11153963 | CGTGTGTGTGTGTGT[A/G]TGTGTGTGTTTTAAG | 9678 |
rs62438684 | snp | A/T | 0.43555 | 0.167544 | intron-variant | PHF14 | GRCh38.p7 | 7:11159228 | ATGTTAAGATTGTTA[A/T]AATGCCATTTATATA | 9678 |
rs62440478 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11054022 | ATGCATGTTGAAGCT[A/C]CAAAAAAAAAAAATC | 9678 |
rs62440479 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11057886 | GTTCTTAAAAAAAAG[A/G]AAAACAAAAAATTGG | 9678 |
rs62440480 | snp | C/T | 0.498525 | 0.0271165 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064517 | TTTTATTTAATATAC[C/T]GTGTTTACTTTCTCA | 9678 |
rs62440483 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11073467 | ACTAGTACAATGGGT[A/G]GGCTCCAAATGCTTT | 9678 |
rs62440485 | snp | C/T | 0.493703 | 0.0557558 | intron-variant | PHF14 | GRCh38.p7 | 7:11083375 | TAGGTGTGTGCACAC[C/T]GTCTCTCTTTCTCCC | 9678 |
rs62440486 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085382 | TTGAATATCAGGACT[A/G]CTGATTTTAAAACAT | 9678 |
rs62440487 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11087652 | CTAATTATATTGTGG[A/G]TTATAACCACAACTA | 9678 |
rs62440509 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11091657 | CAGCTACTCCGGAGG[C/T]TGAGGTGGAAGAATC | 9678 |
rs62440510 | snp | G/T | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104976 | TTCCTCTAGATAAAA[G/T]AATTAGTAATTTCAT | 9678 |
rs62440512 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11131550 | TTTTGAATGCCAGTC[C/T]TTTATCAGATATGTG | 9678 |
rs62440513 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:11133029 | CCTGTATGAGAGAAA[C/G]TACAAAATTCTAATA | 9678 |
rs62440515 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11133885 | ATAGAAGAGTTTGTA[C/G]GAAATAATTTTGGAG | 9678 |
rs63281161 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092101 | ACCTCTGTGTATAAA[-/T]TAATACTTATCTCTG | 9678 |
rs66497859 | in-del | -/T | 0 | 0 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971935 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCAC | 9678 |
rs66936990 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046646 | GCTATTAAAGTTTTT[-/A]ACAGGTATTATAACT | 9678 |
rs67368185 | snp | A/T | 0.233818 | 0.249476 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958267 | TTTTTAATATTATCC[A/T]TTTGCTAAATATGTG | 9678 |
rs67424072 | snp | G/T | 0.237303 | 0.249677 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064540 | CTTTCTCAAGTTCTT[G/T]TAAACTGATGTTTAT | 9678 |
rs68095928 | in-del | -/TTTA | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11027722 | GTTGTCTTAAAGATA[-/TTTA]AAACATGCATGATTT | 9678 |
rs71023881 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10991777 | TTTTTTTTTTTTTTT[-/T]GGTAGAGGCAGGGTT | 9678 |
rs71023882 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11000357 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 9678 |
rs71023886 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076568 | TTTTTTTTTTTTTTT[-/T]GAGGCAGAGTCTCAC | 9678 |
rs71023887 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11087209 | TTCTTTTTTTTTTTT[-/T]AAGATGGAGTCTCGC | 9678 |
rs71023888 | in-del | -/TTT | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11089762 | ATTGTTCATGCATTC[-/TTT]TTTTTTTTTTTTTTT | 9678 |
rs71023889 | in-del | -/TATATATATATATATATATATATACACACACACA | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11122353 | ATATATATATATATA[lengthTooLong]CACACACACACACAC | 9678 |
rs71023891 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11129549 | TTTTTTTTTTTTTTT[-/T]GCCTTTACATAAAAT | 9678 |
rs71023892 | in-del | -/A/ATT | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11145297 | CTCTTTTTCTCTCTT[-/A/ATT]TTTTAAAATTCCATT | 9678 |
rs71249099 | in-del | -/AAAG | 0.438526 | 0.164189 | intron-variant | PHF14 | GRCh38.p7 | 7:11072699 | TGTTTACATTGCTAT[-/AAAG]AAATACCTGAGGCTA | 9678 |
rs71274290 | in-del | -/ATTA | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11141893 | TCTCACAGAAGCAGT[-/ATTA]ATTTTCAATTGTGAC | 9678 |
rs71536831 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10985409 | GAAATATATAATTAT[A/C]CCATATTTAGTTTAT | 9678 |
rs71536832 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10985837 | TTTGTATTTTTAGTA[A/G]AGGTGGGGTTTCACC | 9678 |
rs71536833 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10985989 | GTTTATTTTTTTTGA[A/G]ACAGATTCTCGCTTT | 9678 |
rs71536834 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10987973 | GTGAGCCGAGATCCC[A/C]CCATTGCACTCCAGC | 9678 |
rs71536836 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11028442 | TAATTTTAATTATGG[G/T]TGTATTATTATTTAT | 9678 |
rs71536837 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11028445 | TTTTAATTATGGTTG[G/T]ATTATTATTTATTAT | 9678 |
rs71536838 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11043084 | TCTCTTGTTTTATTG[G/T]TCAGAATTTCTCAAA | 9678 |
rs71536839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11050213 | AAGATGTGAATTTTG[A/G]TGGAACGAAATCAAA | 9678 |
rs71536840 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11089778 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTGAGACG | 9678 |
rs71550873 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971934 | TATATTAGTACAGAC[-/T]TTTTTTTTTTTTTTT | 9678 |
rs71550874 | in-del | -/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11000960 | TTATCTAGATTTTCT[-/C]CCCGTGTTATTTTCT | 9678 |
rs71550875 | in-del | -/GAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002458 | TTTATTTATTTTTGA[-/GAC]GGAGTTTTGCTCTTG | 9678 |
rs71550878 | in-del | -/TATT | 0.437824 | 0.164991 | intron-variant | PHF14 | GRCh38.p7 | 7:11027720 | TAGTTGTCTTAAAGA[-/TATT]TAAAACATGCATGAT | 9678 |
rs71550879 | in-del | -/TT | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11034539 | AATTTCTTAATTCTA[-/TT]TTTTTTTTTTTTTTT | 9678 |
rs71550880 | in-del | -/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11047258 | ATTTTTAGTAGAGAT[-/G]GGGGTTTCACCGTGT | 9678 |
rs71550882 | in-del | -/A | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11150410 | CCTTTCAAGTGTATA[-/A]TTTTCTTGAGAATGG | 9678 |
rs71807051 | in-del | -/T | 0.44768 | 0.153045 | intron-variant | PHF14 | GRCh38.p7 | 7:11069540 | TGCCTCTTTTATGTA[-/T]TTTTTTTAATTTTAT | 9678 |
rs71906497 | in-del | -/AG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152662 | CGTAATAAGAAAAAC[-/AG]AAAATCTGCTGTCGT | 9678 |
rs71913035 | in-del | -/TGAA | 0.198324 | 0.244601 | intron-variant | PHF14 | GRCh38.p7 | 7:11041093 | ATATTTTATTTTACT[-/TGAA]TGAATTGTAGAGTTT | 9678 |
rs72502289 | in-del | -/AAAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072700 | GTTTACATTGCTATA[-/AAAG]AATACCTGAGGCTAG | 9678 |
rs73063409 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:10976980 | AAATGATTGTATTTA[A/C]AATGATTAGTAGTCA | 9678 |
rs73063416 | snp | A/C/G | 0.0170316 | 0.0907494 | intron-variant | PHF14 | GRCh38.p7 | 7:10996974 | GTAGGTATCACCAAT[A/C/G]GGTGGCCAAATTAAG | 9678 |
rs73063417 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11003316 | ACCATTTGAATGACT[C/T]GTCTTTTTCTCCAGT | 9678 |
rs73063418 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | PHF14 | GRCh38.p7 | 7:11003412 | AAATACATAGGTGTT[A/G]AGCCAGTGTTTACCG | 9678 |
rs73063433 | snp | A/C | 0.158302 | 0.232576 | intron-variant | PHF14 | GRCh38.p7 | 7:11047983 | GGAAAAGAGAAAAAC[A/C]TCTTGGTATTTCAAC | 9678 |
rs73063442 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | PHF14 | GRCh38.p7 | 7:11059706 | TTGAACCTGGGAGGC[A/G]GAAACTACAGTGAGC | 9678 |
rs73063450 | snp | A/T | 0.158302 | 0.232576 | intron-variant | PHF14 | GRCh38.p7 | 7:11070128 | TTCTCTTTTTGTTTG[A/T]GACAAGGTCTCATGA | 9678 |
rs73063455 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF14 | GRCh38.p7 | 7:11074649 | TCACTCTTAAGTTCA[A/G]ACTTCCATAGATCCC | 9678 |
rs73063468 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11088418 | AACACACACACACAC[A/G]CACACACACACACAG | 9678 |
rs73065406 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11141121 | TCATCAGGGAATGAA[C/T]TGGTTCTCCAAGGTT | 9678 |
rs73065407 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11141729 | GTATGTAAATCTCTA[C/T]GTGATTATTGGTATT | 9678 |
rs73065414 | snp | A/G | 0.15698 | 0.23205 | intron-variant | PHF14 | GRCh38.p7 | 7:11155578 | CTCATTGCATTAGTC[A/G]TTTTTTGGAGAGTAG | 9678 |
rs73065419 | snp | C/T | 0.175576 | 0.238665 | intron-variant | PHF14 | GRCh38.p7 | 7:11158026 | ATACCCTTTACCCAG[C/T]TTCTCTTTAGGTTAA | 9678 |
rs73065421 | snp | C/T | 0.244776 | 0.249945 | intron-variant | PHF14 | GRCh38.p7 | 7:11158211 | TTTGTCATTATGTCT[C/T]CTCAATCTCTTCCAG | 9678 |
rs73065489 | snp | C/T | 0.162253 | 0.234095 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170246 | CCTCTTTACTCTCCC[C/T]GGTTCTAATTTCCAA | 9678 |
rs73277321 | snp | A/T | 0.00557542 | 0.0525036 | | | GRCh38.p7 | 7:10969717 | ATAGGGTACACTGTT[A/T]TCTGCTTCTCAAAAC | 9678 |
rs73277325 | snp | C/G | 0.00597247 | 0.0543191 | | | GRCh38.p7 | 7:10970173 | GTCATGCATAAATAT[C/G]TTGAATTTGAATACC | 9678 |
rs73277328 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10974647 | GCTGCCTTTGAAACT[A/G]CCCGTGGAGCTGTCC | 9678 |
rs73277668 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11094423 | CAACTTCTTGCAGCT[A/C]TAGTCACATCTATTT | 9678 |
rs73277669 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11095409 | GCTGCTTCTCAAAAA[A/G]TAATTTGCTCTGAGG | 9678 |
rs73277678 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11098293 | ATTTCTTGATCCATT[C/G]TTTTCCTTTCCCATT | 9678 |
rs73277699 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | PHF14 | GRCh38.p7 | 7:11115041 | ATTTTTCCCTTATTT[C/T]TTCTTCCATCCGTTC | 9678 |
rs73279406 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10981749 | ATAATTTCTCTTGCA[A/G]CTTCCTTTTTCTGTG | 9678 |
rs73279409 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10984316 | GCAGTTTATATTTGG[A/T]TTATAAACATTGGTT | 9678 |
rs73279443 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10998334 | GCAGAGAGTGGGACA[G/T]TGGGGAGTTAGAGAT | 9678 |
rs73281188 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11034234 | TAAAACTCTACTTAG[A/G]GACACTTTTGACATA | 9678 |
rs73283110 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11071417 | GCCAGTTTTCCAGTT[G/T]CATTTTCTCTCATTT | 9678 |
rs73283115 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11078488 | CTGCGAGCCAGTTTT[C/G]TCATTCATAGAATGA | 9678 |
rs73283121 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11083256 | CTTTGCTGAGAAATC[C/G]TTTGTCTGAGTGTTT | 9678 |
rs73284602 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11129413 | TTAATAGTACCTGTT[C/G]ACAGATTTCTTTGGA | 9678 |
rs73286506 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11132387 | GTTTCACTTAGTCTT[A/G]TGTCCTCCAGGTCCA | 9678 |
rs73286507 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | PHF14 | GRCh38.p7 | 7:11133203 | GATTTTGACAAACTG[A/G]TTCTCAAGTTTATAT | 9678 |
rs73286509 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11140685 | AGACTACCATTTCAA[A/G]CAAGGAAGTTGAAAT | 9678 |
rs73286514 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | PHF14 | GRCh38.p7 | 7:11142046 | TATTTTTAGATTGGG[G/T]TTTTTTAAATTTCTT | 9678 |
rs73286515 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11147583 | TCTCAATGTTATTTA[A/G]CAATGTCAACCATTC | 9678 |
rs73286519 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | PHF14 | GRCh38.p7 | 7:11151966 | TCCTCATAAGATTTA[A/G]GAAGTATACCACAAT | 9678 |
rs73286520 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11152032 | GAAGGAGAGTTAATA[C/T]GTTTACCAAAATTTT | 9678 |
rs73286523 | snp | C/G | 0.158632 | 0.232706 | intron-variant | PHF14 | GRCh38.p7 | 7:11153419 | GGAAGTTTAGGGTTG[C/G]GAATCAAGAATTTGG | 9678 |
rs73286525 | snp | G/T | 0.158632 | 0.232706 | intron-variant | PHF14 | GRCh38.p7 | 7:11153551 | GATATAAATGGGAAA[G/T]TCATCATAAAGTAGT | 9678 |
rs73286533 | snp | A/G | 0.154993 | 0.231244 | intron-variant | PHF14 | GRCh38.p7 | 7:11162451 | TTCATGTTTATGGAA[A/G]TATATAAATTTATAG | 9678 |
rs73286535 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11164372 | ACAGTGGGAAAACAA[G/T]AAAATGTGGCAAAGC | 9678 |
rs73286537 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | PHF14 | GRCh38.p7 | 7:11166670 | TTTAATATTATACTC[C/T]AGCAATTAGAGTGGA | 9678 |
rs73286539 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11167224 | CATACGGTGGAGAAA[C/G]TTAGTAGACTGTCCG | 9678 |
rs73286542 | snp | A/C/G | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:11168544 | TGTTTGATGATATTG[A/C/G]TGATTATTACTGTTG | 9678 |
rs73678529 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956732 | GAAGACAGAGGCCGA[A/G]ACTGGAGTTATGCTA | 9678 |
rs73678530 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958971 | TAAGAAGGAATTCCT[C/T]TGGACGATGTAGGAG | 9678 |
rs73678531 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967241 | TGACATGGGATGAAA[C/T]TAATTTAGAGTAGTA | 9678 |
rs73678532 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967467 | TTTTGCCACAGGGCC[A/G]AAGAATTATCTGGCC | 9678 |
rs73678533 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967904 | AATGTATTACCACTG[A/C]ATGTCTTGGACTACC | 9678 |
rs73678534 | snp | C/T | 0.0368353 | 0.130617 | | | GRCh38.p7 | 7:10969943 | AGCTATTTATTTTAC[C/T]ATCTTTTGTTGGAGT | 9678 |
rs73678535 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | PHF14 | GRCh38.p7 | 7:10978032 | TCTACCCCTATCCCC[C/G]ACCAGGCAAAGTAAA | 9678 |
rs73678537 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PHF14 | GRCh38.p7 | 7:10979056 | ATGAACAGAATTAGA[C/T]TGATGAAATTGATGA | 9678 |
rs73678538 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:10980710 | TTTATTTCTCATACT[C/T]TGTAAATAGGATTTA | 9678 |
rs73678540 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:10987137 | TATTAATCAGTTGTC[C/T]TTTTACACATTGCAA | 9678 |
rs73678542 | snp | A/C | 0.039522 | 0.134904 | intron-variant | PHF14 | GRCh38.p7 | 7:10996641 | TCACATGATTCATTA[A/C]ATAAATATAAAATAC | 9678 |
rs73678543 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | PHF14 | GRCh38.p7 | 7:10996735 | GAAGGACCACACTAC[C/T]TAAATAAATCCTGGG | 9678 |
rs73678545 | snp | A/C | 0.077417 | 0.180873 | intron-variant | PHF14 | GRCh38.p7 | 7:10998593 | AGTAAACATGGTTGA[A/C]TATATGTGTATTTTT | 9678 |
rs73678546 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | PHF14 | GRCh38.p7 | 7:10999969 | AATTCATTAGAATTG[A/G]AGACCTATTTTTGTT | 9678 |
rs73678547 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | PHF14 | GRCh38.p7 | 7:11000034 | ATTGATGCATAAATA[A/G]GGAAGCTGAATAGTC | 9678 |
rs73678558 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PHF14 | GRCh38.p7 | 7:11010253 | AATGTTTTGTTCTTT[C/T]ATTGGAAATAAAACT | 9678 |
rs73678559 | snp | A/G | 0.039522 | 0.134904 | intron-variant | PHF14 | GRCh38.p7 | 7:11011015 | AGCATAAGGATAACA[A/G]TTAAACAGTTGCTTG | 9678 |
rs73678561 | snp | C/T | 0.101301 | 0.200969 | intron-variant | PHF14 | GRCh38.p7 | 7:11011458 | GTTAAATGTTTCTCA[C/T]TGTGGCTTATTTAAT | 9678 |
rs73678562 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | PHF14 | GRCh38.p7 | 7:11012829 | AAAGAATAATTTAAA[A/T]TTTTTGAACAGATTA | 9678 |
rs73678564 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PHF14 | GRCh38.p7 | 7:11021547 | GTAGTACTTGTGTAC[C/T]ACATTTTAAGAAGGT | 9678 |
rs73678565 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:11022103 | ATATATTAAAAAAGG[C/T]TCAGAGCAGTTTTTA | 9678 |
rs73678566 | snp | C/G | 0.039522 | 0.134904 | intron-variant | PHF14 | GRCh38.p7 | 7:11026419 | TGTTTTATTGTGATA[C/G]TTTATTGAAGTGGTC | 9678 |
rs73678568 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | PHF14 | GRCh38.p7 | 7:11039527 | ATAAATTACAGTTTT[C/T]GCAAATATTTTTTAT | 9678 |
rs73678569 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11041414 | AGAAGTTTAGAAGAT[A/G]CTGGTGTTTTTGTGT | 9678 |
rs73678570 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | PHF14 | GRCh38.p7 | 7:11046042 | CTAGTAAAGAATATT[A/T]TTAATAGGTGGGTGA | 9678 |
rs73678571 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11050858 | CCTTTTTTTTCCCCC[A/G]ACACTTCTTGGAGTC | 9678 |
rs73678573 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11061730 | TTTATATTTATTATT[A/T]ATTAAACATTAGATA | 9678 |
rs73678574 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | PHF14 | GRCh38.p7 | 7:11062511 | CTTTTTATTGACAAG[A/G]ACTTAATTAGCACTT | 9678 |
rs73678575 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063820 | AGATTTTTGAATAGT[A/G]TTACTCTATGTTATT | 9678 |
rs73678576 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | PHF14 | GRCh38.p7 | 7:11071879 | ATTCATTCTTCAACT[C/G]AGTACTTTTAATTTT | 9678 |
rs73679293 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11090834 | AAGGATAAAGAAGTC[G/T]TCATATAAACCAAGG | 9678 |
rs73679297 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11094406 | CCTTGGTTCATGACC[A/C]CCAACTTCTTGCAGC | 9678 |
rs73679299 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11098436 | CTTCTGATTATCTCT[C/G]CCTTGGATCCCTCTC | 9678 |
rs73679301 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103552 | ACTCAATCTTGAACT[A/G]ATTTAGAAGAGACTC | 9678 |
rs73679503 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | PHF14 | GRCh38.p7 | 7:11154219 | TAAGGAATACTGATA[C/T]TTACCATTTATGTAT | 9678 |
rs73679504 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PHF14 | GRCh38.p7 | 7:11155954 | CTATATTATGAAATA[C/T]TGGGAAAAACTTTAT | 9678 |
rs73679507 | snp | A/G | 0.046775 | 0.145601 | intron-variant | PHF14 | GRCh38.p7 | 7:11158673 | CTAGTATTTTCATAC[A/G]AACAATGGGGATTTA | 9678 |
rs73681603 | snp | C/G/T | 0.0330924 | 0.124946 | intron-variant | PHF14 | GRCh38.p7 | 7:11108546 | GAGAGTTCCACATGT[C/G/T]GACTAAGTAATTCTG | 9678 |
rs73681605 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11108786 | TTAGCTGGAATTTCA[C/T]AGCTATATCAACAAG | 9678 |
rs73681606 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11109980 | ATTCATTTGTGTTTT[A/T]AACTTCTTTATATCT | 9678 |
rs73681608 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11114520 | TAGCACATGAAAGCG[G/T]AAATACACCTAAATA | 9678 |
rs73681609 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11120131 | AGATAGAGTAATTTA[A/C]ATTATATAGAAAGTT | 9678 |
rs73681611 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11120773 | ATTTATTTTATAAGT[A/G]GAGAGAATGATATTT | 9678 |
rs73681613 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11134553 | TGATCTCATCCAAGC[A/G]CTTTATTTTACAGAT | 9678 |
rs74274151 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061777 | TTTTTGTTTTTTTTT[-/TT]GTTTTTTTCCAGAGA | 9678 |
rs74296791 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958625 | AATGAGCCATTCTCC[A/G]TAACAAAGGATTTAT | 9678 |
rs74325402 | snp | A/C | 0.0414363 | 0.137845 | | | GRCh38.p7 | 7:10969081 | TTGATGATTCATCAC[A/C]TGGATGAATTTATTA | 9678 |
rs74330943 | snp | A/G | 0.081446 | 0.184634 | intron-variant | PHF14 | GRCh38.p7 | 7:11121358 | ACAGCATTTATGCAA[A/G]AGAAAACCTTACACT | 9678 |
rs74337780 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | PHF14 | GRCh38.p7 | 7:11028356 | ATTAGAAGTGGAACT[A/G]TTGTAAACTGGGGAC | 9678 |
rs74360109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11094052 | CCTTAAAGGAGAAGG[A/G]TCTGGGTGAGACTTT | 9678 |
rs74392191 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:11041292 | TACTTTCTTTGCTCA[A/G]TATTTTCGGTGTTCA | 9678 |
rs74425508 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | PHF14 | GRCh38.p7 | 7:11111062 | TTTGAACACATGATT[A/G]TACATATACGTTCAT | 9678 |
rs74436980 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11131667 | ATTTTTTTCTCTTAT[A/G]GATTATATTTTTGGT | 9678 |
rs74450063 | snp | G/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11149019 | ATAGGGTTTTTTTTT[G/T]GTTTTGTTTTGTTTT | 9678 |
rs74450803 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11028274 | GAAAACAGAATGGTC[A/G]TATGGGTACTGAAAG | 9678 |
rs74491987 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11016851 | TCTTTCCACTTTTTC[A/G]ACTCATTAACCATCT | 9678 |
rs74498732 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155771 | TACAATGTTTTTTTT[-/TT]GTTTTTTTTTAGCAA | 9678 |
rs74523043 | snp | C/G | 0.0748431 | 0.178382 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968638 | TTCATTATAGGTATA[C/G]TGGTTCTGATGGTTG | 9678 |
rs74571222 | snp | A/T | 0.0832709 | 0.186283 | intron-variant | PHF14 | GRCh38.p7 | 7:11024246 | GCTGCAGAAGAAAGG[A/T]TGAAAGGTAGCAGAG | 9678 |
rs74590765 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11001075 | TTTATTTTTGTTACG[A/T]GTATACGGTCTGTCT | 9678 |
rs74591356 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11114649 | TTCTCTGTCTCATCA[A/G]CTCTTCATAAACCTA | 9678 |
rs74593345 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | PHF14 | GRCh38.p7 | 7:11010503 | TATATATGATACATA[C/T]AATTATGTATTAAAG | 9678 |
rs74597858 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | PHF14 | GRCh38.p7 | 7:11050879 | TCTTGGAGTCTGTTT[C/G]TATAGTTTCTTTAAG | 9678 |
rs74600250 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11079750 | TGTATGCTAACTGTG[A/T]TATACAAAATCATTT | 9678 |
rs74604585 | snp | A/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149205 | CCATCACAGTTGTTT[A/T]AAAAGATGTATTCAT | 9678 |
rs74615258 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11074833 | ACAATACTCTAAGAA[A/G]TTCCAAATTGTCCCT | 9678 |
rs74641166 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:10983489 | TCACAGGACTGCTGA[A/G]TGGTGCTGAGTGCAT | 9678 |
rs74679896 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | PHF14 | GRCh38.p7 | 7:11032556 | ATCTAGAGGACCACA[A/G]GCTAAACTTAATCCA | 9678 |
rs74698347 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:10987782 | GTCTTCAGAAATATA[C/G]TAACAACAGTTGATA | 9678 |