SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14819 | snp | A/G | 0 | 0 | utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:67922094 | GTTTCTTAAATTCAA[A/G]GAAATAGCTCTAAAG | 26091 |
rs14840 | snp | C/T | 0.00975586 | 0.0691575 | utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:67922874 | ACTATTTGTGTTTTT[C/T]TTGTGGTGATGAATT | 26091 |
rs471341 | snp | A/G | 0.475525 | 0.107882 | intron-variant | HERC4 | GRCh38.p7 | 10:68068453 | gttacccaggctggc[A/G]tgcagtggtgtgatc | 26091 |
rs474391 | snp | G/T | 0.141934 | 0.225437 | intron-variant | HERC4 | GRCh38.p7 | 10:67963972 | GGTTCTCTAAAGGAA[G/T]AGTTTGAGAAGCTTT | 26091 |
rs482806 | snp | C/G | 0.499722 | 0.0117779 | intron-variant | HERC4 | GRCh38.p7 | 10:68032181 | TAATTATCTGGTAAA[C/G]GTTAACTGAATGCTT | 26091 |
rs483507 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | HERC4 | GRCh38.p7 | 10:67967825 | TTAAATAAACATCAC[A/C]ATGAGGAAACAATCA | 26091 |
rs497849 | snp | A/G | 0.115788 | 0.21092 | intron-variant | HERC4 | GRCh38.p7 | 10:67993863 | TAAGGAATGGGAATA[A/G]GATAACAGGGATAGA | 26091 |
rs499092 | snp | A/G | | | intron-variant, upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075120 | TCCCAGGGGCCGGGG[A/G]GGGGAGCAGCGGACC | 26091 |
rs501169 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | HERC4 | GRCh38.p7 | 10:68023747 | ataaatagtcaatta[C/T]cctagcaccattAAA | 26091 |
rs503677 | snp | A/G | 0.438666 | 0.164028 | intron-variant | HERC4 | GRCh38.p7 | 10:68067255 | ATACATTTCTCTAAC[A/G]GTAGTCATCTGTTTG | 26091 |
rs506460 | snp | G/T | 0.0966517 | 0.197444 | intron-variant | HERC4 | GRCh38.p7 | 10:68066938 | TGTGCACTAGTATTT[G/T]ACCTGCCTCAAACAG | 26091 |
rs507160 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | HERC4 | GRCh38.p7 | 10:68034694 | AGGATGCCCCAGACT[C/G]AATTCATGACCCCCA | 26091 |
rs515489 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:68004027 | aaatggcttttatct[A/G]aaagagggcaataac | 26091 |
rs519204 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HERC4 | GRCh38.p7 | 10:68041316 | AATTTTGAAAAATTT[A/G]TCTCAGAATAGGGGA | 26091 |
rs521935 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | HERC4 | GRCh38.p7 | 10:68041027 | TCTGCTAAAGCATAT[C/T]AATTATGGAATATGT | 26091 |
rs524256 | snp | A/G | 0.444666 | 0.15686 | intron-variant | HERC4 | GRCh38.p7 | 10:67993276 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 26091 |
rs526333 | snp | C/T | 0.480618 | 0.0965156 | intron-variant | HERC4 | GRCh38.p7 | 10:67993002 | TAGCTTTTGTTCTAT[C/T]TTTTTTAAATCATCT | 26091 |
rs534251 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | HERC4 | GRCh38.p7 | 10:68007125 | gatctagaaaatagc[C/T]tcaaaagggcaaatc | 26091 |
rs534611 | snp | G/T | 0.438526 | 0.164189 | intron-variant | HERC4 | GRCh38.p7 | 10:68073590 | AGTTGGCTAAATTTT[G/T]CACTGTGTATATTTG | 26091 |
rs540894 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | HERC4 | GRCh38.p7 | 10:68021093 | cgtagaattcattgg[A/G]gcttatggatgttta | 26091 |
rs542411 | snp | G/T | 0.438526 | 0.164189 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68012803 | ATTTTTgatactgaa[G/T]ttttacaaattgaag | 26091 |
rs542704 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | HERC4 | GRCh38.p7 | 10:68030203 | atctgcccgcctctg[C/T]ctcccagaatgctgg | 26091 |
rs544425 | snp | A/G | 0.499218 | 0.0197529 | intron-variant | HERC4 | GRCh38.p7 | 10:68020717 | cagtggcgcgatctc[A/G]gctcattgcaagctc | 26091 |
rs544508 | snp | A/G | 0.49925 | 0.0193545 | intron-variant | HERC4 | GRCh38.p7 | 10:68020693 | caagctccgcctccc[A/G]ggttcacgccattct | 26091 |
rs545435 | snp | C/G | 0.400147 | 0.19989 | intron-variant | HERC4 | GRCh38.p7 | 10:68028445 | ttgttcttctgagag[C/G]accgtagtaatcttt | 26091 |
rs548787 | snp | C/T | 0.437824 | 0.164991 | intron-variant | HERC4 | GRCh38.p7 | 10:68052573 | aacaagaacctggac[C/T]tgtctatcctgtatg | 26091 |
rs560523 | snp | C/T | 0.438246 | 0.16451 | intron-variant | HERC4 | GRCh38.p7 | 10:68047287 | GAAACAGAAATGGCC[C/T]GTGGAGAAATGCAAA | 26091 |
rs562961 | snp | C/T | 0.483708 | 0.088773 | intron-variant | HERC4 | GRCh38.p7 | 10:68033196 | ACTTCATGATAGTTA[C/T]ACCCACAGGAGCCTA | 26091 |
rs562994 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68049583 | tttttttgggggcag[G/T]gtctcactctgtcac | 26091 |
rs565447 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | HERC4 | GRCh38.p7 | 10:67967008 | TACAAGCACCCGCCA[C/T]CATGACCGGCTAATT | 26091 |
rs566192 | snp | C/T | 0.471673 | 0.115589 | intron-variant | HERC4 | GRCh38.p7 | 10:67967054 | AGAGACGGAGTTTCA[C/T]CGTGTTAGCCAGGAT | 26091 |
rs567987 | snp | C/T | 0.438526 | 0.164189 | intron-variant | HERC4 | GRCh38.p7 | 10:68005773 | gaggctgcagtgagc[C/T]atgattgtgccactg | 26091 |
rs568006 | snp | C/T | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68012327 | tatcaaaagcccaga[C/T]aggctgaaagcaagg | 26091 |
rs574391 | snp | A/G | 0.437824 | 0.164991 | intron-variant | HERC4 | GRCh38.p7 | 10:68052137 | TGAAAAATGAATTCA[A/G]AAGGCAATTTTTTCC | 26091 |
rs584613 | snp | C/G | 0.480697 | 0.0963277 | intron-variant | HERC4 | GRCh38.p7 | 10:68002880 | GCTGGGATTACAAGC[C/G]TGAGCCACCGTGCCT | 26091 |
rs586540 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | HERC4 | GRCh38.p7 | 10:68034450 | ATCACATAACAAGGA[A/G]TAATCTCATTTCCTT | 26091 |
rs592114 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | HERC4 | GRCh38.p7 | 10:68047939 | tttttgttttttttt[G/T]tgtgagacagggtct | 26091 |
rs593024 | snp | C/T | 0.438526 | 0.164189 | intron-variant | HERC4 | GRCh38.p7 | 10:68048150 | tcatgaactcctggg[C/T]tcaagtgctcctccc | 26091 |
rs596682 | snp | C/T | 0.0970103 | 0.197722 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075936 | ATGAATCAGGGACTG[C/T]AGCCAATGTGTAATT | 26091 |
rs597889 | snp | A/G | 0.480775 | 0.0961398 | intron-variant | HERC4 | GRCh38.p7 | 10:67964676 | aaatccaaattccta[A/G]tcctagtttactaaa | 26091 |
rs599870 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HERC4 | GRCh38.p7 | 10:68003939 | ccatactgttctcca[C/T]agtggctatactaat | 26091 |
rs608300 | snp | A/G | 0.47614 | 0.106587 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069640 | CTAATAAGGAATGAA[A/G]GAGAAAGAGGTAGCC | 26091 |
rs612131 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | HERC4 | GRCh38.p7 | 10:67965580 | GCAACCTGATTCCGG[A/G]AGGTGGGAGTATCCT | 26091 |
rs619973 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | HERC4 | GRCh38.p7 | 10:67991463 | CTTAATTTTTAAAAT[A/T]CCATGTTTTAAAGCA | 26091 |
rs623494 | snp | A/G | 0.438526 | 0.164189 | intron-variant | HERC4 | GRCh38.p7 | 10:68050291 | CAAGCTTCTCAATGT[A/G]TATTTAAATTGCTTT | 26091 |
rs625576 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68011582 | gcagtattttgaaag[A/C]aatctttttactgag | 26091 |
rs631322 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | HERC4 | GRCh38.p7 | 10:68037535 | AATATGATGTTTAGC[C/T]TTCTTTATTTCTATG | 26091 |
rs634546 | snp | C/T | 0.437824 | 0.164991 | intron-variant | HERC4 | GRCh38.p7 | 10:68056952 | TTTAAGGTCTGAACC[C/T]AAGTAAGTGCAAGCA | 26091 |
rs636550 | snp | C/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68018329 | attaaaaacttaaca[C/T]ccattcacaataaaa | 26091 |
rs655017 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:68007004 | ccttgcacttgaata[C/T]tgatatttttcttta | 26091 |
rs659082 | snp | C/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68045669 | GTCAGGTTTTTTTAC[C/T]AGTATCACAAGTTTT | 26091 |
rs659420 | snp | C/T | 0.438526 | 0.164189 | intron-variant | HERC4 | GRCh38.p7 | 10:67974631 | GCACTTTAAAAGGAT[C/T]GGTCTATATCTGTTG | 26091 |
rs660640 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:68000408 | GTATTTTTTGTAGAG[A/T]TGGGGTTTTACCATG | 26091 |
rs669322 | snp | A/T | 0.0970103 | 0.197722 | intron-variant | HERC4 | GRCh38.p7 | 10:68052130 | TGAATTCAGAAGGCA[A/T]TTTTTTCCACTTGTG | 26091 |
rs669794 | snp | A/T | 0.499218 | 0.0197529 | intron-variant | HERC4 | GRCh38.p7 | 10:67969257 | aacagggtaccagaa[A/T]tggctcatttgtggc | 26091 |
rs672383 | snp | A/G | 0.439085 | 0.163545 | intron-variant | HERC4 | GRCh38.p7 | 10:67981733 | gaggccaaggcgggt[A/G]gattacttgaggcca | 26091 |
rs674486 | snp | C/T | 0.474272 | 0.110462 | intron-variant | HERC4 | GRCh38.p7 | 10:68060160 | GCACAGTACCTGGCA[C/T]ATAATGGAGGTTTAC | 26091 |
rs679645 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | HERC4 | GRCh38.p7 | 10:68021045 | gaagaagtaatagcc[A/C]aaaactcccaaatat | 26091 |
rs684284 | snp | A/C | 0.481087 | 0.0953875 | intron-variant | HERC4 | GRCh38.p7 | 10:67982091 | ataccaatgacattg[A/C]tcacagaaataggaa | 26091 |
rs685634 | snp | A/G | 0.437542 | 0.165312 | intron-variant | HERC4 | GRCh38.p7 | 10:68053428 | tggtcccagctactc[A/G]ggaggctgaagcagg | 26091 |
rs689211 | snp | A/C | 0.480697 | 0.0963277 | intron-variant | HERC4 | GRCh38.p7 | 10:68047843 | cttacaaaagtaaat[A/C]tactcttaccatatg | 26091 |
rs747024 | snp | C/T | 0.152001 | 0.229992 | intron-variant | HERC4 | GRCh38.p7 | 10:68042943 | GCAGAAATACCTTAA[C/T]ATACAGCTTAAAGTT | 26091 |
rs863110 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67972252 | aaaggccaggcacgg[G/T]ggctcacaccggtaa | 26091 |
rs863874 | snp | C/T | 0.438666 | 0.164028 | intron-variant | HERC4 | GRCh38.p7 | 10:68036577 | GCCCTTTATAACAGA[C/T]TTCTCTTTTTATTTC | 26091 |
rs865248 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68062068 | TTACTTAACAGGTTA[A/G]AACTGGGAGAAGTCT | 26091 |
rs866255 | snp | A/G | 0.489684 | 0.0710729 | synonymous-codon, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68014084 | TTTTACAGTAAAGGG[A/G]CTTTTCCTGTTGCTT | 26091 |
rs1097165 | snp | C/T | 0.1472 | 0.227886 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68075226 | cgcttgcctcccgtt[C/T]ttccccgcccgctcc | 26091 |
rs1104020 | snp | C/T | 0.0582 | 0.160352 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68075239 | gtgctctccgccccg[C/T]ttgcctcccgttctt | 26091 |
rs1149674 | snp | G/T | 0.0248432 | 0.108648 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069866 | tttagtagggacggg[G/T]tttcaccgtgttagc | 26091 |
rs1191993 | snp | A/C | 0.482905 | 0.0908579 | intron-variant | HERC4 | GRCh38.p7 | 10:68028134 | cattatttttcctag[A/C]gttatgagctggaat | 26091 |
rs1204083 | snp | C/G | 0.47743 | 0.103805 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075440 | GGCGCCTGTGGCCAG[C/G]CACCCCCCCCCCCCC | 26091 |
rs1209191 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | HERC4 | GRCh38.p7 | 10:68029662 | TCAATTTTTAAGGAC[A/G]Aatatttatataatt | 26091 |
rs1210158 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68049589 | gagtgagacactgcc[A/C]caaaaaaaaaaaaaa | 26091 |
rs1211222 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68030196 | cgcctctgcctccca[A/G]aatgctgggattaca | 26091 |
rs1490008 | snp | C/T | 0.271702 | 0.249056 | intron-variant, utr-variant-5-prime | HERC4 | GRCh38.p7 | 10:68074698 | GCCGGCCTCTGAAGC[C/T]GTTGCGAGCGGCCGG | 26091 |
rs1812671 | snp | C/T | 0.188631 | 0.242351 | intron-variant | HERC4 | GRCh38.p7 | 10:67973425 | CAAGGCCCAATCCCG[C/T]AGGAATTAGAATAAG | 26091 |
rs1906722 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68048953 | ACTGTTTTGTTTTTA[A/G]ACTAACAGTATACAA | 26091 |
rs1981180 | snp | C/T | 0.27393 | 0.248852 | intron-variant, missense | HERC4 | GRCh38.p7 | 10:68070509 | aagcaattctcctgc[C/T]tcagcctcccgaata | 26091 |
rs1981181 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | HERC4 | GRCh38.p7 | 10:68068953 | TACAACATTCTttca[A/C]atggagtatctcatt | 26091 |
rs2007505 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | HERC4 | GRCh38.p7 | 10:68004328 | CAGAATGGGAGAAAA[C/T]ATTTGCAAACTACCC | 26091 |
rs2029474 | snp | C/T | 0.152334 | 0.230133 | intron-variant | HERC4 | GRCh38.p7 | 10:67992056 | atacaattagctggg[C/T]gtggtggtgcacacc | 26091 |
rs2039700 | snp | C/T | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67955376 | TAGAGTAAGCCAGTA[C/T]AGAACGGTAGTAATA | 26091 |
rs2176102 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68050626 | ATAGCTGACTTTTTA[G/T]ACATCAAATACACAA | 26091 |
rs2308195 | in-del | -/ATAG | 0.0252325 | 0.109451 | intron-variant | HERC4 | GRCh38.p7 | 10:67995355 | TAAGATAACTATATA[-/ATAG]ATAGGGAGAAACTAA | 26091 |
rs2451402 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68062077 | AGGTTAAAACTGGGA[A/G]AAGTCTACAGTTGGA | 26091 |
rs2451403 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061880 | ttttttttttttttt[A/T]aaatggagtctcgct | 26091 |
rs2459115 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:68031180 | TACAAAAGATTAAGA[C/G]AATTAGCATTTCTTA | 26091 |
rs2485677 | snp | C/T | 0.499722 | 0.0117779 | intron-variant | HERC4 | GRCh38.p7 | 10:68031401 | GTAAAATTTAAGACT[C/T]GCCAACAGGAATAAA | 26091 |
rs2485679 | snp | G/T | 0.185788 | 0.241613 | intron-variant | HERC4 | GRCh38.p7 | 10:68051522 | gctagtttttttttg[G/T]ttttttttttgtatt | 26091 |
rs2485680 | snp | A/G | 0.474634 | 0.109726 | intron-variant | HERC4 | GRCh38.p7 | 10:68060108 | AAAAGTCTTGTATCT[A/G]TCCTGCAAAAGTATG | 26091 |
rs2485681 | snp | A/G | 0.0112482 | 0.0741458 | intron-variant | HERC4 | GRCh38.p7 | 10:68062239 | AAATTCACCTTACCA[A/G]AATCTTTTAACTTGC | 26091 |
rs2932413 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67974075 | AAAAAAATTACTGTA[C/T]ACACACACACACACA | 26091 |
rs2943770 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061852 | gtgccctgcactcca[A/G]cctgggcgacagagt | 26091 |
rs3740055 | snp | C/T | 0.252702 | 0.249985 | intron-variant | HERC4 | GRCh38.p7 | 10:68033887 | TACATTTCTCTCTTA[C/T]ACTAAGAATCACTGA | 26091 |
rs3758392 | snp | C/T | 0.499339 | 0.0181672 | intron-variant | HERC4 | GRCh38.p7 | 10:67932573 | CTTTCCATTTAACAA[C/T]ATCAGAGATTAGTTT | 26091 |
rs3758393 | snp | C/T | 0.178144 | 0.239451 | intron-variant | HERC4 | GRCh38.p7 | 10:68032964 | AGCTCAGTAGATAGT[C/T]GTGACTAAATAATTT | 26091 |
rs3814178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:68044745 | ACTATTCAACAAATA[C/T]GTTCCAAACGTAATT | 26091 |
rs3832649 | in-del | -/A | 0.319616 | 0.240112 | intron-variant | HERC4 | GRCh38.p7 | 10:68073904 | ATAATTATAATACAG[-/A]AAAAAAAACATGCAA | 26091 |
rs3834396 | in-del | -/A | 3.81003e-05 | 0.00436448 | splice-acceptor-variant | HERC4 | GRCh38.p7 | 10:68025678 | ACACTCCACCTTCCT[-/A]AAAAAAAGACAAAAC | 26091 |
rs3891387 | snp | C/G | 0.144296 | 0.226554 | intron-variant | HERC4 | GRCh38.p7 | 10:68008151 | GAGAGAGAGTGAGAG[C/G]GAAACTTCATTTGTT | 26091 |
rs4141919 | snp | A/G | 0.0197687 | 0.0974348 | downstream-variant-500B | HERC4 | GRCh38.p7 | 10:67921810 | TCTATAAATTCATGT[A/G]GGAATAGAAACAAGT | 26091 |
rs4303129 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | HERC4 | GRCh38.p7 | 10:67945717 | agttaaagcataaag[C/T]ttttattagttttct | 26091 |
rs4457643 | snp | G/T | 0.266 | 0.249487 | intron-variant | HERC4 | GRCh38.p7 | 10:68006381 | TTTGTTTTTGTTTTT[G/T]TTTTTTTTTTGAGAC | 26091 |
rs4598560 | snp | C/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68007289 | attacatttctaact[C/G]cagaatttctctttg | 26091 |
rs4630186 | snp | A/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68007286 | tcaattacatttcta[A/T]ctccagaatttctct | 26091 |
rs4746721 | snp | C/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67942605 | CAACCTCCACCTCCT[C/G]GGTTCAAGTGATTCT | 26091 |
rs4746722 | snp | G/T | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67942618 | CTCGGTTCAAGTGAT[G/T]CTCCTGGCTCAGCCT | 26091 |
rs4746723 | snp | A/T | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67945970 | GAACACATTTAAAAA[A/T]GGCAGGAATAGCTGG | 26091 |
rs4746726 | snp | C/T | 0.474 | 0.111014 | intron-variant | HERC4 | GRCh38.p7 | 10:68060887 | ATTGTGGGAAGCAAT[C/T]TAAGATCTACTTTAT | 26091 |
rs4746727 | snp | C/T | 0.264084 | 0.249603 | intron-variant | HERC4 | GRCh38.p7 | 10:68061152 | AACTTATAGTTAAAA[C/T]TACTTCAGCTACTAG | 26091 |
rs5785841 | in-del | -/A | 0.0110805 | 0.0736036 | intron-variant | HERC4 | GRCh38.p7 | 10:67991032 | TAAAAAACAGAAAAG[-/A]AAAAAAAAAATAGAA | 26091 |
rs5785843 | in-del | -/A | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68039164 | AAAAAAAAAAAAAAA[-/A]TTAGCAGGTGTGGTG | 26091 |
rs5785844 | in-del | -/A | 0.494143 | 0.0537956 | intron-variant | HERC4 | GRCh38.p7 | 10:68039316 | GTAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 26091 |
rs6480300 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HERC4 | GRCh38.p7 | 10:67944861 | accaagaaaaagaag[C/T]gattagtgagcttga | 26091 |
rs6480301 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:68006111 | ttttattacatctat[G/T]tatatcttattatat | 26091 |
rs6480302 | snp | C/T | 0.316968 | 0.240864 | intron-variant | HERC4 | GRCh38.p7 | 10:68057191 | ACAGTGGGTACACAG[C/T]TTATCAACAACACAC | 26091 |
rs7069710 | snp | C/T | 0.177182 | 0.23916 | intron-variant | HERC4 | GRCh38.p7 | 10:68051785 | accccgcctccgagg[C/T]tcaagtgatcctccc | 26091 |
rs7069772 | snp | A/G | 0.177182 | 0.23916 | intron-variant | HERC4 | GRCh38.p7 | 10:68051655 | tgagccaccatgccc[A/G]gccAATGTTAACACT | 26091 |
rs7071319 | snp | A/G | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67981721 | ccagcactttgggag[A/G]ccaaggcgggtggat | 26091 |
rs7071409 | snp | A/G | 0.438386 | 0.164349 | intron-variant | HERC4 | GRCh38.p7 | 10:67951989 | acaatcttgttctcc[A/G]ccacacctcaatgcc | 26091 |
rs7075378 | snp | A/G | 0.142272 | 0.225598 | intron-variant | HERC4 | GRCh38.p7 | 10:67982555 | gaaactctccaggac[A/G]ttggtctgggcaaaa | 26091 |
rs7077383 | snp | C/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67996359 | GATTagtgcactgtt[C/T]aggattatctccacc | 26091 |
rs7077601 | snp | C/T | 0.163564 | 0.234582 | intron-variant | HERC4 | GRCh38.p7 | 10:67940638 | tggtcatactagtct[C/T]gaactcctgacctcc | 26091 |
rs7080546 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HERC4 | GRCh38.p7 | 10:67983744 | gtgagccaagatcgc[A/G]ccactgcactccagc | 26091 |
rs7080601 | snp | C/T | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67974591 | AAAACTTAAGAGATA[C/T]TGCCTATAGTTCTTA | 26091 |
rs7081996 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | HERC4 | GRCh38.p7 | 10:67941365 | CTTTACAACTGTTTT[C/T]TCCCAGACATAAGCA | 26091 |
rs7086373 | snp | A/G | 0.145305 | 0.227022 | intron-variant | HERC4 | GRCh38.p7 | 10:67972244 | aaaaaaaaaaaggcc[A/G]ggcacggtggctcac | 26091 |
rs7086730 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | HERC4 | GRCh38.p7 | 10:67942176 | TGTTTTAAATAAGAC[C/G]TGGGCTCCAGCCTGG | 26091 |
rs7087233 | snp | C/T | 0.188631 | 0.242351 | intron-variant | HERC4 | GRCh38.p7 | 10:68007654 | atgatctcaattctt[C/T]agtcactgcagccat | 26091 |
rs7087912 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68000870 | cagaaggaagcaact[A/C]taaattcggacttct | 26091 |
rs7087982 | snp | G/T | 0.00284494 | 0.0376082 | intron-variant | HERC4 | GRCh38.p7 | 10:68000714 | ataacccaatgtttt[G/T]tgtccttataaaagg | 26091 |
rs7088830 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67981585 | gctgcagaataaaca[C/T]tgttctccttagcac | 26091 |
rs7097107 | snp | A/G | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67974796 | TAACACCATTACCCT[A/G]CCTCATTCCATGGAG | 26091 |
rs7099201 | snp | A/C/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68041944 | CTTTAATATTATCCA[A/C/T]CCACTGGCATTAAAA | 26091 |
rs7099215 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68072045 | AACTGCCACAGAAAA[G/T]ACTGAAGTGCCATTA | 26091 |
rs7099234 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68072091 | TAAACAGTAAGTCAG[G/T]ATAGCTGCAGTCTCA | 26091 |
rs7477454 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67964611 | caacaaagtgatcat[G/T]caaaaagatcagatt | 26091 |
rs7478614 | snp | A/G | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67945377 | cttcaaacatgaagg[A/G]caaataaagatcttc | 26091 |
rs7894163 | snp | A/C | 0.499923 | 0.00618962 | intron-variant | HERC4 | GRCh38.p7 | 10:67933232 | CCTTGGGTTCCAAGG[A/C]ATCTGAACAAAATTT | 26091 |
rs7894364 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HERC4 | GRCh38.p7 | 10:67963278 | ctggagtgcagtggc[A/G]tgatctcaactcatt | 26091 |
rs7896937 | snp | C/T | 0.480618 | 0.0965156 | intron-variant | HERC4 | GRCh38.p7 | 10:67967098 | TGACCTTGTGATCTG[C/T]CCACCTTGGCCTCCC | 26091 |
rs7897923 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | HERC4 | GRCh38.p7 | 10:67995496 | tgtttcctagtaata[C/T]aaatttcttctttta | 26091 |
rs7902239 | snp | C/G | 0.142433 | 0.227201 | intron-variant | HERC4 | GRCh38.p7 | 10:68035640 | CACTTTAAACAAGGC[C/G]TATAAGGTGCTGTAT | 26091 |
rs7902383 | snp | C/T | 0.480382 | 0.097079 | intron-variant | HERC4 | GRCh38.p7 | 10:67961604 | GCAAATTATCAAACC[C/T]AAGGGTAGTTTGGGG | 26091 |
rs7903659 | snp | G/T | 0.31503 | 0.241394 | intron-variant | HERC4 | GRCh38.p7 | 10:67986720 | TGGTATTTCAATCCT[G/T]ATAGATAATTCTTCA | 26091 |
rs7903731 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67979554 | taatgacagagaact[C/T]cccaaacatagaaaa | 26091 |
rs7905627 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67948136 | ctaatagttgtaaac[A/C]cttaaactaaaaaaa | 26091 |
rs7907843 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | HERC4 | GRCh38.p7 | 10:67959317 | CATCTTATATATCTA[C/T]TAATGTAAGATCTTT | 26091 |
rs7912627 | snp | A/C | 0.137867 | 0.223442 | intron-variant | HERC4 | GRCh38.p7 | 10:67967861 | ATCCTGATTATGAAA[A/C]TTTTATAAGAAAACT | 26091 |
rs7913472 | snp | C/T | 0.131381 | 0.220067 | intron-variant, downstream-variant-500B | HERC4, POU5F1P5 | GRCh38.p7 | 10:68009849 | tttctataatgttca[C/T]agcatcttcaccagc | 26091 |
rs7916902 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:68049379 | TAAAACTTTGGAAAG[A/G]TAAgtcgggcacagt | 26091 |
rs7917123 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | HERC4 | GRCh38.p7 | 10:67938703 | gtaatgccagcactt[C/T]gggaggccgaggcgg | 26091 |
rs7917339 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:68049422 | taatcccaggacttt[C/G]ggaggctgaggtgga | 26091 |
rs7918329 | snp | C/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67986674 | ACTGTATAATGTAAA[C/T]AATACATAAATCTTG | 26091 |
rs7919422 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67974393 | AAACTAAACAAAACT[A/G]GCTAACTTTCCTTTG | 26091 |
rs7920025 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | HERC4 | GRCh38.p7 | 10:68053476 | accccattaattttt[A/T]aattatttgtagaga | 26091 |
rs7922547 | snp | C/T | 0.163892 | 0.234703 | intron-variant | HERC4 | GRCh38.p7 | 10:67948392 | tctcaaaagtagata[C/T]acaaatggcaaaaag | 26091 |
rs9414970 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68057638 | caaaaaaaaaaaaaa[A/G]GGATCCTCAAAATAT | 26091 |
rs9415894 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:68039153 | ctctactgaaaatac[A/C]aaaaaaaaaaaaaaa | 26091 |
rs9633583 | snp | A/T | 0.263535 | 0.249633 | intron-variant | HERC4 | GRCh38.p7 | 10:68006143 | gtatatgtctttaca[A/T]gttgctgtagttatt | 26091 |
rs10047296 | snp | C/T | 0.480382 | 0.097079 | intron-variant | HERC4 | GRCh38.p7 | 10:67952369 | gctcactgcaacctc[C/T]gtctattgggttcaa | 26091 |
rs10430469 | snp | C/T | 0.263809 | 0.249618 | intron-variant | HERC4 | GRCh38.p7 | 10:67966940 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 26091 |
rs10430470 | snp | A/G | 0.263535 | 0.249633 | intron-variant | HERC4 | GRCh38.p7 | 10:67966941 | CTCACTGCAAGCTCT[A/G]CCTCCCGGGTTCACG | 26091 |
rs10509292 | snp | A/C | 0.154661 | 0.231107 | intron-variant, downstream-variant-500B | HERC4 | GRCh38.p7 | 10:67966330 | TAATGCATTCTTAGG[A/C]GTTCCAGTATGAAGA | 26091 |
rs10509293 | snp | A/G | 0.154661 | 0.231107 | intron-variant | HERC4 | GRCh38.p7 | 10:68046029 | CTTCCAGTACATGAA[A/G]TTTATTACACTAATA | 26091 |
rs10605641 | in-del | -/AC | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67996315 | AAGACCTTGAAATAG[-/AC]ACCCCCCCTGCCCCA | 26091 |
rs10651200 | in-del | -/TAACAA | 0.438666 | 0.164028 | intron-variant | HERC4 | GRCh38.p7 | 10:68041150 | TCCAACCACTAATGT[-/TAACAA]TTAGTAAAAAGTTTA | 26091 |
rs10762183 | snp | A/C | 0.480461 | 0.0968913 | intron-variant | HERC4 | GRCh38.p7 | 10:67953540 | GGACTTGGGCACCAA[A/C]CTTAAGAGCTCTCCT | 26091 |
rs10823116 | snp | A/G | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67923688 | CTCAGCTTCTGGAGT[A/G]GCTGGGAGCACAGTC | 26091 |
rs10823117 | snp | A/C | 0.18 | 0.24 | intron-variant | HERC4 | GRCh38.p7 | 10:67926429 | AATAAAAAAAAAAAA[A/C]AACAAAAAAATTAGT | 26091 |
rs10823119 | snp | C/T | 0.438105 | 0.164671 | intron-variant | HERC4 | GRCh38.p7 | 10:67929816 | CACCACACCCAGCTG[C/T]GCATTTTTTTTTTGA | 26091 |
rs10823120 | snp | C/T | 0.499234 | 0.0195537 | intron-variant | HERC4 | GRCh38.p7 | 10:67960325 | actctgccctgtgtg[C/T]ttcttcccttggctg | 26091 |
rs10823121 | snp | C/T | 0.49917 | 0.0203505 | intron-variant | HERC4 | GRCh38.p7 | 10:67962195 | GACATTTAAAAAGTG[C/T]TATTACTACTAAGAA | 26091 |
rs10823122 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67974121 | ACACACACACACACA[C/T]ACACACAGGGTCAGG | 26091 |
rs10823123 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:67994651 | TGGTCAGGCTGGTCT[C/T]GAACTCCCAACCTCA | 26091 |
rs10823124 | snp | A/C | 0.252702 | 0.249985 | intron-variant | HERC4 | GRCh38.p7 | 10:68004832 | TCATTATTACAAGAA[A/C]AGCATGCAGGAAACC | 26091 |
rs10823126 | snp | A/G | 0.262985 | 0.249663 | intron-variant | HERC4 | GRCh38.p7 | 10:68053363 | GGATGGAGTGCAGTG[A/G]TGAAATTACAGCTCA | 26091 |
rs10823127 | snp | C/G | 0.271702 | 0.249056 | intron-variant | HERC4 | GRCh38.p7 | 10:68061643 | TAGCACTTTGGGAGG[C/G]AGAGACGGGCAGATC | 26091 |
rs10823128 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68061961 | GGTGGCAACCATTTA[A/G]ATTACTTTAAATTTA | 26091 |
rs10823130 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | HERC4 | GRCh38.p7 | 10:68073344 | AAAAACCAATCAGTT[G/T]TATTTTTTAAAATGT | 26091 |
rs10997877 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927430 | tatatatatatatat[A/T]ttttttttttttttt | 26091 |
rs10997879 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67931639 | CATGTTGGCAAGGCT[A/G]GCCTGGAACTCCTGA | 26091 |
rs10997881 | snp | C/T | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67937238 | GTATATTAAAAAAAA[C/T]ACTGTGTGATATGAC | 26091 |
rs10997883 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | HERC4 | GRCh38.p7 | 10:67938208 | agcactttgggaggc[C/T]aacgcgggcagatca | 26091 |
rs10997884 | snp | C/T | 0.437965 | 0.164831 | intron-variant | HERC4 | GRCh38.p7 | 10:67938256 | gaccatcctggccaa[C/T]atggtgaaacctcat | 26091 |
rs10997885 | snp | A/G | 0.437965 | 0.164831 | intron-variant | HERC4 | GRCh38.p7 | 10:67938553 | CTGGAGTGCCTTACC[A/G]TAATACTTATGGATT | 26091 |
rs10997887 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67949503 | AAAAAAACAGTAACA[A/C]ACAAAAATCCAACCC | 26091 |
rs10997889 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67958749 | CTTCTCTAATATAAA[A/G]TGTTTTCAGCCACAT | 26091 |
rs10997891 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67967060 | ggagtttcatcgtgt[C/T]agccaggatggtctc | 26091 |
rs10997892 | snp | A/C | 0.188946 | 0.24243 | intron-variant | HERC4 | GRCh38.p7 | 10:67967965 | AGAGGAattctggta[A/C]taaatatggcagaat | 26091 |
rs10997893 | snp | C/T | 0.271702 | 0.249056 | intron-variant | HERC4 | GRCh38.p7 | 10:67970138 | TAATGAAGGTATTTA[C/T]AGCAAATTAAAAATT | 26091 |
rs10997894 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67972187 | CCATTGCACTCCAGT[C/T]TGGGTGACAGGAGTG | 26091 |
rs10997895 | snp | A/G | 0.263809 | 0.249618 | intron-variant | HERC4 | GRCh38.p7 | 10:67976551 | AGCTGCATGGACACC[A/G]ATTTAACAACTATCT | 26091 |
rs10997897 | snp | C/T | 0.158962 | 0.232835 | intron-variant | HERC4 | GRCh38.p7 | 10:67983944 | CTCCAGCCCTGGCAA[C/T]AGAGCAAGATTCCAT | 26091 |
rs10997898 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67988213 | TCCAATTTTAAATTA[A/G]TCATTTGTTTCAAAT | 26091 |
rs10997900 | snp | A/G | 0.439224 | 0.163383 | intron-variant | HERC4 | GRCh38.p7 | 10:67996994 | CTCCGTCTCGAAAAA[A/G]AAAAGAAAAAAAAAG | 26091 |
rs10997903 | snp | C/T | 0.244776 | 0.249945 | intron-variant | HERC4 | GRCh38.p7 | 10:68007466 | GTCACTAGTGCCTTA[C/T]TTCATTGGTTTGGTG | 26091 |
rs10997904 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68011126 | GGAGTGCACTAGTAT[C/G]ATCATAGCTCACTGT | 26091 |
rs10997906 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68019127 | TCAGCCTCCCAAGTA[A/G]CTGGGATTACAGGCA | 26091 |
rs10997907 | snp | A/G | 0.271162 | 0.249103 | intron-variant | HERC4 | GRCh38.p7 | 10:68021386 | AGGAGGAAAAGACAC[A/G]CACAATCATCTGAAT | 26091 |
rs10997908 | snp | A/G | 0.077417 | 0.180873 | intron-variant | HERC4 | GRCh38.p7 | 10:68021439 | TTTCCTGTAAGATCA[A/G]GAATAAGGATGCCTG | 26091 |
rs10997910 | snp | C/T | 0.182614 | 0.240747 | intron-variant | HERC4 | GRCh38.p7 | 10:68023863 | taaaaggcaacacta[C/T]gtttttgaagataac | 26091 |
rs10997911 | snp | A/G/T | 0.0930568 | 0.194599 | intron-variant | HERC4 | GRCh38.p7 | 10:68023917 | CAGGTAGGAAAATAT[A/G/T]TCTTAGAAAATAAAT | 26091 |
rs10997912 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | HERC4 | GRCh38.p7 | 10:68029661 | TTCAATTTTTAAGGA[C/T]GAatatttatataat | 26091 |
rs10997913 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68030200 | atcccagcattctgg[A/G]aggcagaggcgggca | 26091 |
rs10997914 | snp | C/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68030212 | tgggaggcagaggcg[C/G]gcagatcacttgagg | 26091 |
rs10997915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HERC4 | GRCh38.p7 | 10:68031470 | AATCAATAAAATATG[A/G]TAttaggttggtgca | 26091 |
rs10997917 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | HERC4 | GRCh38.p7 | 10:68046020 | CTCCTGAAGCTTCCA[A/G]TACATGAAGTTTATT | 26091 |
rs10997918 | snp | C/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68054302 | TTTTTTTCTTTTCTT[C/G]TTCTTTGTTTTATTA | 26091 |
rs10997919 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68057807 | tgggttcaagcaatt[C/T]tcatgcctcagcctc | 26091 |
rs10997920 | snp | C/T | 0.271432 | 0.24908 | intron-variant | HERC4 | GRCh38.p7 | 10:68059039 | AAATGCAAGTGTGTA[C/T]TTTTCCTTGTTTAAA | 26091 |
rs10997921 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059846 | TATATATTATAATAT[A/T]TTATATATCATAATA | 26091 |
rs10997922 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059847 | ATATATTATAATATA[A/T]TATATATCATAATAT | 26091 |
rs10997923 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059933 | ATCATAATATTATAT[A/T]TTATAATAATATTAT | 26091 |
rs10997924 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059934 | TCATAATATTATATA[A/T]TATAATAATATTATA | 26091 |
rs10997925 | snp | C/T | 0.270351 | 0.24917 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069886 | TCCCTACTAAAAATA[C/T]AAAAAATTACCCGGG | 26091 |
rs10997926 | snp | C/G | 0 | 0 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075831 | CCACCACCACCAGTT[C/G]AGTTTCCTTGTACAG | 26091 |
rs11298676 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68018270 | TTAACAGATTAAAGG[-/A]AAAAAAAATCATAAA | 26091 |
rs11299096 | in-del | -/A | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67996315 | GACCTTGAAATAGAC[-/A]CCCCCCCTGCCCCAC | 26091 |
rs11305276 | in-del | -/A | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67926431 | AAAAAAATAAAAAAT[-/A]AAAAAAAAAAAACAA | 26091 |
rs11327388 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67964092 | CCAGCTACCACTCCA[-/T]TTTTTTTTTTTTTTT | 26091 |
rs11398946 | in-del | -/A | 0.152334 | 0.230133 | intron-variant | HERC4 | GRCh38.p7 | 10:67967914 | AGGTAGCAGGGATTG[-/A]AAAAAAAAAGGAGCT | 26091 |
rs11406155 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67974046 | AGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 26091 |
rs11422072 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68001379 | TTGTATTTAAAAAAA[-/A]AAAAAAATTCCTCTT | 26091 |
rs11422655 | in-del | -/AA | 0.440471 | 0.161928 | intron-variant | HERC4 | GRCh38.p7 | 10:67990456 | GAAAAAAAAAAAAAA[-/AA]GGAAGGCAGGAAGAA | 26091 |
rs11497976 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HERC4 | GRCh38.p7 | 10:67982601 | ACAAGCACATGCAAC[C/T]AAAGCAAAAGTGGAC | 26091 |
rs11527388 | snp | C/T | 0.264084 | 0.249603 | intron-variant | HERC4 | GRCh38.p7 | 10:67979868 | CGTGAACCTGAGAGG[C/T]GGAGCTTGCGGTGAG | 26091 |
rs11527389 | snp | A/G | 0.314787 | 0.241459 | intron-variant | HERC4 | GRCh38.p7 | 10:68021533 | GAAATAAAATGCTGC[A/G]TGCAGTGGCTCATGC | 26091 |
rs11591713 | snp | A/T | 0.444444 | 0.157135 | intron-variant | HERC4 | GRCh38.p7 | 10:68031103 | CTAATTTTGTTAAAA[A/T]TAATGTACACCCAAA | 26091 |
rs11592459 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67932110 | ttacaggcacgtgcc[A/T]ccacacccagctaat | 26091 |
rs11594785 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68006545 | cccagctaatttttt[A/T]atttttatttttagt | 26091 |
rs11595259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67975863 | TATCTGTGGCCAGGA[C/T]ACTCATTTGGGAGAA | 26091 |
rs11596337 | snp | C/T | 0.188631 | 0.242351 | intron-variant | HERC4 | GRCh38.p7 | 10:67983041 | gctgaggcaggagaa[C/T]tgcttgaacccagga | 26091 |
rs11597568 | snp | A/C | 0.116488 | 0.211364 | intron-variant | HERC4 | GRCh38.p7 | 10:68029048 | ccaggcacagtggcg[A/C]ccgtagctccagcta | 26091 |
rs11599081 | snp | A/G | 0.188 | 0.24219 | intron-variant | HERC4 | GRCh38.p7 | 10:68071486 | TTCAGTTATTTCTAT[A/G]GGGCATGCTAAAGTA | 26091 |
rs11812970 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERC4 | GRCh38.p7 | 10:67970435 | tgtccctactgaaaa[C/T]acaaaaactagctgg | 26091 |
rs11813144 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HERC4 | GRCh38.p7 | 10:68062594 | ctgtctctactaaaa[A/C]tacaaaaaaaaaaaa | 26091 |
rs11813416 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERC4 | GRCh38.p7 | 10:67990686 | CACAAACTTAAGCAA[C/T]GTGGTAATGTTAAGT | 26091 |
rs11814547 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HERC4 | GRCh38.p7 | 10:68040105 | AATGAATATACTGTT[A/C]AAGGATAACTACATT | 26091 |
rs11815388 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029889 | gattacaggcgcctg[C/T]caccacgcccggcta | 26091 |
rs11817084 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68020314 | agaaaatataagcca[A/C]caatagaaactatcc | 26091 |
rs11817849 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HERC4 | GRCh38.p7 | 10:67958528 | CAACAAAATGCAAAT[C/T]AAAGCAAAACCTGAC | 26091 |
rs11818664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HERC4 | GRCh38.p7 | 10:67970754 | acataaaaatttgtg[A/G]gatgctaataaatcc | 26091 |
rs11819155 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67941646 | atgagtattatgtca[C/T]taaatgttcttctaa | 26091 |
rs12218640 | snp | C/T | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67947935 | acctggtgatctgcc[C/T]accttggcctcccaa | 26091 |
rs12220297 | snp | A/G | 0.316726 | 0.240931 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68076291 | ATTTTTAGTAGAGAC[A/G]AGGTTTCGCCATATT | 26091 |
rs12221165 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67971961 | gctcatgcctgtaat[C/T]tcagcactttgggag | 26091 |
rs12240313 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HERC4 | GRCh38.p7 | 10:68037941 | gtgtgtacagactga[C/G]aagctaattctaaaa | 26091 |
rs12242880 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | HERC4 | GRCh38.p7 | 10:67931582 | ggtgtgtgccaccac[A/G]cccgattaatttttg | 26091 |
rs12248214 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | HERC4 | GRCh38.p7 | 10:67976146 | tgtatggctcacaaa[A/G]cataaaatacttact | 26091 |
rs12248457 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68064595 | GAGAGAGAGAAAAAA[A/G]GAAAAAGAAAAAAAG | 26091 |
rs12251764 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HERC4 | GRCh38.p7 | 10:67980067 | atgacatttaaagta[C/T]tgaagggaaaattta | 26091 |
rs12252848 | snp | C/T | 0.143284 | 0.226079 | intron-variant | HERC4 | GRCh38.p7 | 10:67948869 | gaggttgcagtgagc[C/T]gagactgtgccactg | 26091 |
rs12253451 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68054370 | tttttttttttttca[A/G]accgagtctcactaa | 26091 |
rs12254112 | snp | A/G/T | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67984408 | acagagacaaatatc[A/G/T]catgttctcacttat | 26091 |
rs12254861 | snp | C/T | 0.141596 | 0.225274 | intron-variant | HERC4 | GRCh38.p7 | 10:68030307 | atagccgggtgtgat[C/T]gtgcatgcctataat | 26091 |
rs12255982 | snp | A/T | 0.0314385 | 0.121371 | utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:67922002 | TAGCAGAAAGTCACA[A/T]GTATTGCATCAACTC | 26091 |
rs12258843 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | HERC4 | GRCh38.p7 | 10:68032159 | ACATTAACATGACTG[C/T]AATAAATAATTATCT | 26091 |
rs12259209 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | HERC4 | GRCh38.p7 | 10:68062617 | aaaaaaaaattagcc[A/G]ggtgtggtggtgggt | 26091 |
rs12260695 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059786 | tatatattataatat[A/T]atatatcataatatt | 26091 |
rs12263299 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68064602 | AGAAAAAAAGAAAAA[A/G]AAAAAAAGACATAAA | 26091 |
rs12263478 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68004689 | gctggggtggcctca[G/T]gagacttataatcat | 26091 |
rs12269420 | snp | A/G | 0.141934 | 0.225437 | intron-variant | HERC4 | GRCh38.p7 | 10:68000158 | ccatcacaccAGCCA[A/G]TAAGTCATCTGAAGG | 26091 |
rs12269442 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HERC4 | GRCh38.p7 | 10:67972461 | gggaggcggaggttg[C/T]ggtgagctgagatcg | 26091 |
rs12355259 | snp | C/T | 0.437965 | 0.164831 | intron-variant | HERC4 | GRCh38.p7 | 10:67944344 | tatccaagaccagga[C/T]agtacctcttagttt | 26091 |
rs12358178 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68014459 | ATACTGAAATCCCTT[A/G]CAATAAACGATTCAG | 26091 |
rs12411712 | snp | A/C | 0.182614 | 0.240747 | intron-variant | HERC4 | GRCh38.p7 | 10:68039077 | GGAGACCAAGGTAGG[A/C]GGATCACTTGAGGTC | 26091 |
rs12412334 | snp | G/T | | | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075434 | GGGGGGGGGGGGGGG[G/T]GGGTGGCTGGCCACA | 26091 |
rs12413347 | snp | A/G | 0.170733 | 0.237101 | intron-variant | HERC4 | GRCh38.p7 | 10:67993103 | TAATCCCAGCACTTT[A/G]GGAGGCTGAGGTGGG | 26091 |
rs12413531 | snp | A/G | 0.177182 | 0.23916 | intron-variant | HERC4 | GRCh38.p7 | 10:68066222 | AGCAGTTTTAAAAAT[A/G]CATGCCTTTGTGAGA | 26091 |
rs12413999 | snp | C/T | 0.237303 | 0.249677 | intron-variant | HERC4 | GRCh38.p7 | 10:68060490 | GTGATCCACCCGCCT[C/T]GACCTCCCAAAGTTC | 26091 |
rs12414281 | snp | A/G | 0.200801 | 0.245111 | intron-variant | HERC4 | GRCh38.p7 | 10:67955812 | ATAAGGAATGATCTG[A/G]CTAAGGAAGCATTAC | 26091 |
rs12414598 | snp | A/C | 0.188631 | 0.242351 | intron-variant | HERC4 | GRCh38.p7 | 10:67986511 | GCATGCACCACCATA[A/C]CCAGCTAATTTTTTT | 26091 |
rs12414741 | snp | C/T | 0.177182 | 0.23916 | intron-variant | HERC4 | GRCh38.p7 | 10:68053142 | cctataaaatcacca[C/T]gaacattgacttagc | 26091 |
rs12414751 | snp | G/T | 0.188631 | 0.242351 | intron-variant | HERC4 | GRCh38.p7 | 10:68023116 | acagggcagttacta[G/T]gagaaacagtatggc | 26091 |
rs12415059 | snp | A/G | 0.20111 | 0.245173 | intron-variant | HERC4 | GRCh38.p7 | 10:67927598 | ACCCAGCTAATTTTC[A/G]TATTTTTAGTAGAGA | 26091 |
rs12415155 | snp | C/T | 0.182614 | 0.240747 | intron-variant | HERC4 | GRCh38.p7 | 10:68024120 | tgtatctacactata[C/T]aaataactactatga | 26091 |
rs12571730 | snp | G/T | 0.108402 | 0.206034 | intron-variant | HERC4 | GRCh38.p7 | 10:68046697 | ATAGTCCAGGCGAGG[G/T]AGCTCACATCTATAA | 26091 |
rs12761264 | snp | C/T | 0.40157 | 0.198813 | intron-variant | HERC4 | GRCh38.p7 | 10:68021594 | tgggcagatcaccag[C/T]ggtcaggagttcaag | 26091 |
rs12761462 | snp | C/T | 0.19646 | 0.2442 | intron-variant | HERC4 | GRCh38.p7 | 10:68016438 | GCTCACTGCAACCTC[C/T]GCCTCCCGGATTCAA | 26091 |
rs12762422 | snp | C/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67981874 | tgaatcgggggggtg[C/G]aggttgcagtgagcc | 26091 |
rs12762950 | snp | G/T | 0.185472 | 0.241529 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68076644 | ggcttctctgctagc[G/T]tctggtggttgccaa | 26091 |
rs12763190 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68004160 | gagaaatgcatattt[A/G]gatcttttgcccatt | 26091 |
rs12764436 | snp | C/T | 0.176861 | 0.239062 | intron-variant | HERC4 | GRCh38.p7 | 10:68064886 | CTGAGACAGGAGAAT[C/T]GCTTGAATCCAGGAG | 26091 |
rs12765430 | snp | C/T | 0.176861 | 0.239062 | intron-variant | HERC4 | GRCh38.p7 | 10:68064658 | ttgcagtattactta[C/T]aacaaaaatctggaa | 26091 |
rs12766485 | snp | C/T | 0.200801 | 0.245111 | intron-variant | HERC4 | GRCh38.p7 | 10:67925518 | TCAGAAAATTCCCTT[C/T]CTCTGTATTCATGAA | 26091 |
rs12767358 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67973750 | CCCTGGGTAAGAGTA[A/C]TTTTAAAAATTACTG | 26091 |
rs12767952 | snp | A/G | 0.176861 | 0.239062 | intron-variant | HERC4 | GRCh38.p7 | 10:68061641 | CCTAGCACTTTGGGA[A/G]GCAGAGACGGGCAGA | 26091 |
rs12768839 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67952821 | aggagaatggcatga[A/C]cctgggaggcagagc | 26091 |
rs12769018 | snp | C/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67952878 | gtactccagcctggg[C/G]gacagagggagactc | 26091 |
rs12769628 | snp | C/T | 0.188316 | 0.242271 | intron-variant | HERC4 | GRCh38.p7 | 10:67968862 | TTTTAACACTGCTCT[C/T]ATTAACTGATAGAAA | 26091 |
rs12770220 | snp | C/T | 0.177182 | 0.23916 | intron-variant | HERC4 | GRCh38.p7 | 10:68049708 | ttgaatccaggagtt[C/T]gaaaccagcctcggc | 26091 |
rs12771631 | snp | A/C | 0.188316 | 0.242271 | intron-variant | HERC4 | GRCh38.p7 | 10:67979483 | cccaaaagggcaaat[A/C]taagttactggcctt | 26091 |
rs12772936 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HERC4 | GRCh38.p7 | 10:67950050 | caaaacaaaaaaCAA[A/C]AAAAAAGGAAAACCA | 26091 |
rs12773188 | snp | C/T | 0.437965 | 0.164831 | intron-variant | HERC4 | GRCh38.p7 | 10:67926517 | TTATCCAGCCGCAGT[C/T]GGCTTTAACTTTCAG | 26091 |
rs12776006 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68020152 | tgactcctgacacag[A/C]taaaacctacaatga | 26091 |
rs12778020 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67980205 | caaccttcgccttcc[A/C]gatagtcatcaaaac | 26091 |
rs12778641 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029792 | cgaccaggctggagt[A/G]cagtggcacagcctc | 26091 |
rs12778649 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029771 | tttgagacagagtct[C/T]gctgtcgaccaggct | 26091 |
rs12778660 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029825 | ctcactgcaacctcc[A/G]cctcccaggttcaag | 26091 |
rs12778825 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029824 | gctcactgcaacctc[C/T]acctcccaggttcaa | 26091 |
rs12778856 | snp | C/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029866 | gcctcagcctcccga[C/G]tacctgggattacag | 26091 |
rs12779924 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029676 | CGAatatttatataa[G/T]ttttatatattatat | 26091 |
rs12779925 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68029677 | GAatatttatataat[C/T]tttatatattatata | 26091 |
rs12783464 | snp | A/G | 0.481009 | 0.0955756 | intron-variant | HERC4 | GRCh38.p7 | 10:67998507 | agccgagatcctgcc[A/G]ctgcattacagcctg | 26091 |
rs12784085 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68051521 | agctagttttttttt[G/T]gttttttttttgtat | 26091 |
rs12785138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68051523 | ctagtttttttttgg[G/T]tttttttttgtattt | 26091 |
rs16924989 | snp | A/G | 0.200492 | 0.245049 | intron-variant | HERC4 | GRCh38.p7 | 10:67954262 | GTAGATAAATCAATG[A/G]TCCCTAATGATAAAT | 26091 |
rs16924996 | snp | C/T | 0.170408 | 0.236992 | intron-variant | HERC4 | GRCh38.p7 | 10:67960724 | TGGATTTGTGGTCCA[C/T]ATCCATCAGCTCATA | 26091 |
rs16925001 | snp | C/T | 0.170733 | 0.237101 | intron-variant | HERC4 | GRCh38.p7 | 10:67960983 | TTCATCACTTTCTTG[C/T]GGATTTGGCGGACCT | 26091 |
rs16925007 | snp | A/G | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67965693 | CAGAGGTGCTGGTTG[A/G]CTGACAAGAGCACCC | 26091 |
rs16925017 | snp | C/T | 0.188631 | 0.242351 | intron-variant | HERC4 | GRCh38.p7 | 10:67988353 | CTAACAAAAACCATA[C/T]AATGCAAACTAACAA | 26091 |
rs16925034 | snp | A/G | 0.182614 | 0.240747 | intron-variant | HERC4 | GRCh38.p7 | 10:68038732 | TCAATTTTTTTACTC[A/G]GGAAATTTACTCAAT | 26091 |
rs16925037 | snp | A/G | 0.182933 | 0.240836 | intron-variant | HERC4 | GRCh38.p7 | 10:68040080 | CTATAGTGCCTAATT[A/G]ATAGTACGTAATGAA | 26091 |
rs16925043 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | HERC4 | GRCh38.p7 | 10:68040242 | AAGGCTTGTAACACA[C/T]ATTAAATGCTAATAT | 26091 |
rs16925049 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | HERC4 | GRCh38.p7 | 10:68044139 | ACCCACTAAAAAAAT[G/T]TGTAATGAAGCAAGT | 26091 |
rs17454621 | snp | C/T | 0.093417 | 0.194889 | intron-variant | HERC4 | GRCh38.p7 | 10:67927049 | TATTTGTAGCCATGA[C/T]TTATCTTAATCACTG | 26091 |
rs17533770 | snp | C/T | 0.154661 | 0.231107 | intron-variant | HERC4 | GRCh38.p7 | 10:67974682 | ATAATGTATGCTTAT[C/T]GTTAATTTTTCGTAA | 26091 |
rs17533847 | snp | C/T | 0.154993 | 0.231244 | intron-variant | HERC4 | GRCh38.p7 | 10:67986883 | ATGAACTTCTAGATC[C/T]AGGGGCATAAAATAA | 26091 |
rs17533917 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | HERC4 | GRCh38.p7 | 10:67990840 | AATTAGGCTATAAAC[A/G]TATAAAACAAAAGAA | 26091 |
rs28427439 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059771 | TATATATCATAATAT[A/T]ATATATTATAATATT | 26091 |
rs28451754 | snp | C/T | 0.29789 | 0.24537 | intron-variant | HERC4 | GRCh38.p7 | 10:68059870 | CATAATATTATATAT[C/T]ATAATAATATTATAT | 26091 |
rs28499873 | snp | A/C | | | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68070285 | TTAGTTAAAAACATT[A/C]TTAAAATTTAGTTAA | 26091 |
rs28565181 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68051520 | CAGCTAGTTTTTTTT[G/T]GGTTTTTTTTTTGTA | 26091 |
rs28614059 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059855 | TAATATATTATATAT[C/T]ATAATATTATATATT | 26091 |
rs28635766 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927428 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 26091 |
rs34009718 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059960 | TTATATTATATTTTG[G/T]TTCTCTTGCTATTAT | 26091 |
rs34013177 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67997330 | CTATGCTTTATGTTG[G/T]CTTTATTGTCCTTTA | 26091 |
rs34019082 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68022723 | TTAAAGCTTCATGCA[-/T]TCAAAAGACACTATC | 26091 |
rs34027809 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68051342 | AAAATGTTAACACTA[-/T]TTTTTTTTTTTTTTT | 26091 |
rs34053728 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061908 | AAAAAAAAAAAAAAA[A/T]TCTGTATATAAAAAT | 26091 |
rs34092198 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061948 | CAAAACAGATAGAGG[G/T]GGCAACCATTTAGAT | 26091 |
rs34105506 | in-del | -/A | 0.438666 | 0.164028 | intron-variant | HERC4 | GRCh38.p7 | 10:67945621 | AAAACATGAACCAAT[-/A]AAAAAATAATAACTA | 26091 |
rs34123712 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68031516 | TTTACCATTAATGGC[-/A]AAAAAATGAAATTAC | 26091 |
rs34135809 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67976258 | CAAACTCTTTCTACT[-/A]AAAAAAGAAATATAC | 26091 |
rs34136710 | in-del | -/G | | | utr-variant-5-prime, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68073163 | CTCTTCTGAAACCCC[-/G]GGAAAGTTGGAGGTA | 26091 |
rs34144591 | snp | A/T | 0.115438 | 0.210697 | intron-variant | HERC4 | GRCh38.p7 | 10:67989686 | GACAATTAGAAAAAT[A/T]AAAGTGAGAAAACTT | 26091 |
rs34152706 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68052012 | CATATAAAAAGGGTG[-/A]AAAAAAAGTATCATT | 26091 |
rs34157958 | in-del | -/A | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67962224 | AAAGTTTAAATAAGC[-/A]AAAAAAAAAAAGCCT | 26091 |
rs34163024 | snp | C/T | 0.177824 | 0.239355 | intron-variant | HERC4 | GRCh38.p7 | 10:68028309 | GCAATAAGTTTTGCT[C/T]ATATTGATTTGCAAG | 26091 |
rs34189806 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67947862 | TTAAACAATACACTC[-/T]TTTTTTTTTTTTTTT | 26091 |
rs34204741 | snp | A/C | 0.201727 | 0.245295 | intron-variant | HERC4 | GRCh38.p7 | 10:67947001 | CCGCTAAAGAGAGAG[A/C]GAGAGACCCCAATAC | 26091 |
rs34241026 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68051051 | AAAACGGAGAGTTAA[-/G]GGGGGGATTAAACCA | 26091 |
rs34267546 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68039009 | TTTTCAAGAAAAAAA[-/G]GGGGGATGCCAGATG | 26091 |
rs34363369 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | HERC4 | GRCh38.p7 | 10:67965886 | GTATCTAACTGCTTA[C/T]CCATTTCTGCATTAA | 26091 |
rs34390019 | in-del | -/T/TT/TTT | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67964091 | CCAGCTACCACTCCA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 26091 |
rs34400006 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67940883 | AGCTTTCTGTACCTT[-/C]CCCCACTTTTTACCT | 26091 |
rs34490316 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67973203 | GAATGGAAAACATTT[-/A]AAAAAAAAAGGTTTG | 26091 |
rs34497566 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67947287 | TGGAAAACAGTTATT[-/G]CCATGTAAATAGTAA | 26091 |
rs34505719 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68060920 | TCGTTATGCCATCCT[-/A]AAAAAAAAAAAGTCA | 26091 |
rs34538237 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67988626 | TCTGTTAATAGGAAT[-/G]GGGGAAAGAGGAAAA | 26091 |
rs34560535 | in-del | -/TAAA | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68022543 | AAATAAATAAATAAA[-/TAAA]ATTCAAATAGATCAA | 26091 |
rs34573894 | snp | C/T | 0.200492 | 0.245049 | intron-variant | HERC4 | GRCh38.p7 | 10:67941461 | AAAGTAATACACATT[C/T]GAAATTTGGAAAACA | 26091 |
rs34603437 | in-del | -/A | 0.411746 | 0.190626 | intron-variant | HERC4 | GRCh38.p7 | 10:68000576 | GAGCCAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 26091 |
rs34612885 | in-del | -/A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68001372 | TGAGACCTTGTATTT[-/A/T]AAAAAAAAAAAAAAT | 26091 |
rs34622887 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68003342 | AATTTTTTTTTTTTT[G/T]TTTGTATTTTTAGTA | 26091 |
rs34624828 | in-del | -/A | 0.43978 | 0.162738 | intron-variant | HERC4 | GRCh38.p7 | 10:68047201 | ATTGACTTCTTAGGG[-/A]AAAAAAAAAAAAGGT | 26091 |
rs34625908 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68008536 | TGCTGCTGACCGGTT[-/G]GGGGATGTAATCATA | 26091 |
rs34673496 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67937231 | AGGTAAGGTATATTA[-/A]AAAAAATACTGTGTG | 26091 |
rs34682741 | in-del | -/C | 0.49925 | 0.0193545 | intron-variant | HERC4 | GRCh38.p7 | 10:67982491 | CAAAATGATTAATGA[-/C]TTAAATCTAAGACCT | 26091 |
rs34727639 | in-del | -/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68055769 | CTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 26091 |
rs34779824 | in-del | -/A | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68068510 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCATGGT | 26091 |
rs34787166 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68052002 | TCAAACTGTTCATAT[-/A]AAAAGGGTGAAAAAA | 26091 |
rs34787842 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061560 | AAAAAAAAAAAAAAA[A/G]GGAATAGGTTTCTGT | 26091 |
rs34790645 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061018 | TAATTCTGCTCTTTA[-/G]GACCGCTTTTAGCCT | 26091 |
rs34797132 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68027760 | CACTTCGTCTCTACT[-/A]AAAAATACAAAAATT | 26091 |
rs34813698 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68030810 | CTGCAAATAAACTTG[-/A]AAAAAAATGTGACAT | 26091 |
rs34829503 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68053591 | CACAGCACCCGGCCT[-/G]GGGGACCATTTTAAA | 26091 |
rs34842253 | in-del | -/CA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67978313 | TCAAGGAAACACTGG[-/CA]GTATTCTGGCAGTAC | 26091 |
rs34860013 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67972953 | TACTGCTGTTACACA[-/G]GAAAAATGCCTGTAT | 26091 |
rs34861126 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68065777 | GATAAGAGGATTCCT[-/G]GAACCCAGGGAAGTC | 26091 |
rs34883094 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67996395 | TGTCTTTGAGCTATT[-/C]CACAATTCTGTAAAT | 26091 |
rs34910021 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67949390 | AATTCTCAAACTCTT[-/C]CCAAAAGATCACAGC | 26091 |
rs34912130 | in-del | -/AT | | | intron-variant | HERC4 | GRCh38.p7 | 10:68027991 | ATTATATTTTTAATT[-/AT]ATATATATATATATA | 26091 |
rs34940978 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68033225 | TACTTAAAAGCCTGG[-/A]AAAAAAAATGTACTT | 26091 |
rs34948748 | in-del | -/T/TT | | | intron-variant | HERC4 | GRCh38.p7 | 10:68018901 | AAAACCCCACAAGGC[-/T/TT]TTTTTTTTTTTTTTT | 26091 |
rs34966031 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68035156 | AAGAGACAACCACTC[-/T]TTTTTTTTTTTTTTT | 26091 |
rs34981836 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67970591 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 26091 |
rs35054670 | in-del | -/A | 0.492237 | 0.0618148 | intron-variant | HERC4 | GRCh38.p7 | 10:68038353 | ACAAGAGCTAGATAC[-/A]AAAAAAAAAAAATTA | 26091 |
rs35054860 | in-del | -/CTAT | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67995356 | GCATTAGTTTCTCCC[-/CTAT]TATTATATAGTTATC | 26091 |
rs35099795 | snp | C/T | 0.188 | 0.24219 | intron-variant | HERC4 | GRCh38.p7 | 10:68074457 | TCCCATATTTAAAAA[C/T]AAAATAAGAGTAATA | 26091 |
rs35100976 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68045185 | ATTAGCTGGGTGTGT[-/G]GGTGGTGCACGCCTG | 26091 |
rs35105661 | in-del | -/T | 0.499609 | 0.0139722 | intron-variant | HERC4 | GRCh38.p7 | 10:68037092 | GGAACCTATTTCTTC[-/T]TTTTTTTTTTTTTTT | 26091 |
rs35133402 | snp | A/G | 0.0729246 | 0.176477 | synonymous-codon, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68014174 | TGAAGGAACAAAAGC[A/G]GAAGTGTGCTGCCTA | 26091 |
rs35148717 | snp | A/G | 0.110519 | 0.207473 | intron-variant | HERC4 | GRCh38.p7 | 10:67986495 | GTAGTTGGAATTACA[A/G]GCATGCACCACCATA | 26091 |
rs35151790 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67986184 | AAAGAGATGTTTAAG[-/A]AAAGTCATACCAGTA | 26091 |
rs35180777 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68002158 | ATATGAGCTTAACTG[-/A]AAAAGCCTTTTAATT | 26091 |
rs35182511 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67947864 | TTTTTTTTTTTTTTG[G/T]ATTTTTAGCAGAGAC | 26091 |
rs35223188 | snp | G/T | 0.116838 | 0.211584 | intron-variant | HERC4 | GRCh38.p7 | 10:68016029 | GATCACTTGAACCTG[G/T]AAGGCAGAGGTTGCA | 26091 |
rs35224629 | snp | G/T | 0.00802475 | 0.0628329 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68034062 | ATGGGCTCCTCCTGC[G/T]GCAACTTGCATGAAA | 26091 |
rs35242757 | in-del | -/CA | | | frameshift-variant | HERC4 | GRCh38.p7 | 10:67925162 | TAGGATGTTCTGCCC[-/CA]AATATTCCCCTTTGT | 26091 |
rs35278971 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061914 | AAAAAAAAAATCTGT[A/T]TATAAAAATTCAGGT | 26091 |
rs35316574 | in-del | -/A | 3.36618e-05 | 0.00410241 | intron-variant | HERC4 | GRCh38.p7 | 10:67936254 | TTAATTTAAATTTTT[-/A]AAAAAAGTCAATGTC | 26091 |
rs35329650 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68073266 | TGCTAGGCTACAATA[-/G]ATTGCTACATGGTAA | 26091 |
rs35331321 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67944140 | TTACCATGAGCCTTA[A/G]GTGAGACCCAGTGCT | 26091 |
rs35349032 | in-del | -/T | | | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069740 | GCTTTCTGACACAAG[-/T]TTTAAAGTTCTTGTG | 26091 |
rs35415602 | in-del | -/AGAG | 0.438806 | 0.163867 | intron-variant | HERC4 | GRCh38.p7 | 10:67963996 | AGCTTTACCTAGGTC[-/AGAG]AGAGATGAAGAAAAA | 26091 |
rs35422015 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68045198 | GTGGTGGTGCACGCC[-/T]TGTGATCCCAGCTAT | 26091 |
rs35447930 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:68053393 | CTGCAGCAGCAACCT[-/C]CCCAGGCTCAGGTGA | 26091 |
rs35448851 | in-del | -/A/AA/CA | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67983785 | GGAAGACTCTGTCTC[-/A/AA/CA]AAAAAAAAAAAAAAA | 26091 |
rs35472959 | snp | G/T | 0.00463653 | 0.0479246 | synonymous-codon | HERC4 | GRCh38.p7 | 10:67936179 | GTTAACAGCTGTGTC[G/T]GCACCATTTAGAACC | 26091 |
rs35496892 | snp | A/C | 0.480931 | 0.0957637 | intron-variant | HERC4 | GRCh38.p7 | 10:67945817 | AAACTCAAATCAAAA[A/C]ACATACGACAGATAC | 26091 |
rs35517209 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67957459 | ATTTACTTAATATAC[-/A]AAAAAAGTACCATTA | 26091 |
rs35541518 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:68016510 | GCATGTGCCACCATG[-/C]CCCAGCTAATTTTTG | 26091 |
rs35632333 | in-del | -/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67978311 | CCTCAAGGAAACACT[-/G]GCAGTATTCTGGCAG | 26091 |
rs35662615 | snp | A/T | 0.481087 | 0.0953875 | intron-variant | HERC4 | GRCh38.p7 | 10:67945821 | TCAAATCAAAAAACA[A/T]ACGACAGATACACGA | 26091 |
rs35697772 | in-del | -/C | 0.480775 | 0.0961398 | intron-variant | HERC4 | GRCh38.p7 | 10:68021051 | TAATAGCCAAAAACT[-/C]CCCAAATATGGGGAA | 26091 |
rs35720011 | snp | A/C/G | 0.000644127 | 0.0179348 | missense, synonymous-codon, intron-variant, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:67990239 | TGGTGCCTTTTCTAG[A/C/G]TTCACAAGAGCTGTA | 26091 |
rs35735995 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67972685 | AAATTTTTAAAAGAA[-/T]TATGCAAGATCCTTG | 26091 |
rs35768029 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68026841 | GAAAGACTCCGTCTC[-/A]AAAAAAAAAAATTAG | 26091 |
rs35781027 | in-del | -/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68003364 | ATTTTTAGTAGAGAT[-/G]GGGGTTTCACTGTGT | 26091 |
rs35799834 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68076393 | AGGCGTGAGCCACCG[G/T]TCCTGGCCTGTTTCT | 26091 |
rs35811740 | in-del | -/T | 0.438246 | 0.16451 | intron-variant | HERC4 | GRCh38.p7 | 10:67965839 | GTATACACAAATGGC[-/T]AGCAAATAAGAGTAG | 26091 |
rs35817479 | in-del | -/T | 0.483995 | 0.0880135 | intron-variant | HERC4 | GRCh38.p7 | 10:68019013 | CCAAAGCATTCTTTC[-/T]TTTTTTTTTTTTTTT | 26091 |
rs35880990 | snp | C/T | 0.115788 | 0.21092 | intron-variant | HERC4 | GRCh38.p7 | 10:68060625 | CTATACAATGCAGTA[C/T]CAACTTATAATGTGT | 26091 |
rs35923280 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67996562 | TTGTTTACATGGGTT[-/A]AAAATCATTAATACT | 26091 |
rs35936049 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:68040410 | TTGTTTTAGCTTTTA[-/C]GAAATTAAAAAATAC | 26091 |
rs35954815 | snp | A/T | 0.196149 | 0.244131 | intron-variant | HERC4 | GRCh38.p7 | 10:68002176 | AAGCCTTTTAATTAT[A/T]AAAAAAACATCAAGT | 26091 |
rs36006838 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67995016 | TTTAATCACTACTCG[-/A]AAAAGTTTGAGAAAC | 26091 |
rs36054589 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67923998 | GGGAACTAAGGCCTG[-/A]AAAAGCTTTATTTTA | 26091 |
rs36089296 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68003345 | TTTTTTTTTTTTTTT[G/T]TGTATTTTTAGTAGA | 26091 |
rs36181074 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67972420 | CAGCTACTCGGGAGG[A/C]TGAGACAGAAGAATC | 26091 |
rs41274094 | snp | A/G | 0.156319 | 0.231784 | intron-variant | HERC4 | GRCh38.p7 | 10:67954114 | CATAAGGTCACTGTT[A/G]TAATTACTTAAACTC | 26091 |
rs41274096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:67955295 | TAAAACTTAATAAAC[C/T]GAGCATAAAGAGTAC | 26091 |
rs41274098 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HERC4 | GRCh38.p7 | 10:67955351 | TATAATGTATAACTC[A/G]TAACACCATTAGAGT | 26091 |
rs41274100 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | HERC4 | GRCh38.p7 | 10:67966429 | TTTCACACTTGTAGG[G/T]TTTTTTTGTCTTGTT | 26091 |
rs41274102 | snp | A/C | 4.95929e-05 | 0.00497936 | missense, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68014061 | CCATTATAGGGGTAC[A/C]AATTTCCTTTTACAG | 26091 |
rs41278494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68040087 | GCCTAATTAATAGTA[C/G]GTAATGAATATACTG | 26091 |
rs41278496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069356 | ACATGAAAGTGAAAC[A/G]GACATTCACTTCTCT | 26091 |
rs41307561 | snp | G/T | 0.154329 | 0.23097 | intron-variant | HERC4 | GRCh38.p7 | 10:67936346 | AACTACTAAATTTGA[G/T]ATAAAATTCTGCTAC | 26091 |
rs55638343 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67999883 | AGTCTCCCTTCATTA[G/T]TAATATATTTATAAA | 26091 |
rs55699934 | snp | A/C | 0.173643 | 0.238054 | intron-variant | HERC4 | GRCh38.p7 | 10:67927164 | TTTATGGAATTTATT[A/C]AACTGTTTGAATTAA | 26091 |
rs55984730 | in-del | -/TA | 0.340333 | 0.233109 | intron-variant | HERC4 | GRCh38.p7 | 10:68027990 | ATATATATATATATA[-/TA]ATAAAAATAAGTCAA | 26091 |
rs56061311 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HERC4 | GRCh38.p7 | 10:68040143 | TCTTGGAGGCTTTAG[C/T]ATTAGTCATAAAATT | 26091 |
rs56078104 | snp | A/G | 0.131723 | 0.220251 | intron-variant | HERC4 | GRCh38.p7 | 10:68072489 | AAGTAAAAAGCTTCC[A/G]TCTTGTTTTCCTCCC | 26091 |
rs56121517 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927426 | TATATATATATATAT[A/T]TATATTTTTTTTTTT | 26091 |
rs56282922 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68023012 | TAGGTATTATAAAAA[A/G]AAAAAGAAAAAGGCA | 26091 |
rs56338838 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:67942083 | CTGACACACTGAAAA[C/T]GTTTATTTTTTTCCC | 26091 |
rs56682038 | snp | C/T | 0.170408 | 0.236992 | intron-variant | HERC4 | GRCh38.p7 | 10:67932040 | TCAGCTCACTGCAAC[C/T]TCCGCCTCCCAGGTT | 26091 |
rs56715366 | snp | A/G | 0.144296 | 0.226554 | intron-variant | HERC4 | GRCh38.p7 | 10:67957799 | TAGACAGTTCTTTAT[A/G]GTCTGAATCTGCATT | 26091 |
rs56827249 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68039008 | GTTTTCAAGAAAAAA[A/G]GGGGGGATGCCAGAT | 26091 |
rs56864415 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HERC4 | GRCh38.p7 | 10:68023218 | GAACTGAAAGTGGGG[C/T]CCTGAAGGGATGTTT | 26091 |
rs57067657 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67945816 | TAAACTCAAATCAAA[A/C]AACATACGACAGATA | 26091 |
rs57091641 | snp | A/G | 0.132409 | 0.220618 | intron-variant | HERC4 | GRCh38.p7 | 10:67968582 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCA | 26091 |
rs57200026 | snp | G/T | | | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075424 | CGAATCTTCCGGGGG[G/T]GGGGGGGGGGGGGTG | 26091 |
rs57243869 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68027523 | TTCACAAAATCAATA[C/T]TAATTTCTTAATATC | 26091 |
rs57274189 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927416 | TATATATATATATAT[-/A]TATATATATATATAT | 26091 |
rs57338183 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68047741 | CACCAGTTGTGATGT[C/T]AAGGATGTGAAGCAA | 26091 |
rs57439929 | snp | A/T | 0.0704125 | 0.17392 | intron-variant | HERC4 | GRCh38.p7 | 10:68074183 | ACACAAATAACAGAG[A/T]CCACTTCATCTATAC | 26091 |
rs57454971 | in-del | -/CACA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67974117 | ACACACACACACACA[-/CACA]TACACACAGGGTCAG | 26091 |
rs57468056 | in-del | -/C | 0.141934 | 0.225437 | intron-variant | HERC4 | GRCh38.p7 | 10:67971503 | ACTATCAATGAATTT[-/C]ACAATATTTCTAAAA | 26091 |
rs57497479 | in-del | -/CA/CACA/CACACACA | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67946397 | ACACACACACACACA[-/CA/CACA/CACACACA]AGACCCAATGATCTG | 26091 |
rs57549701 | in-del | -/TT | | | intron-variant | HERC4 | GRCh38.p7 | 10:68003346 | TTTTTTTTTTTTTTT[-/TT]GTATTTTTAGTAGAG | 26091 |
rs57572487 | snp | C/G | 0.132066 | 0.220435 | utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:67922586 | TAAAGGTTTTTCACT[C/G]AATGATTGAAGAAAA | 26091 |
rs57621406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68039837 | GACCTGTTCAGCATA[C/T]TAAGTATTTTAGGAA | 26091 |
rs57705644 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68070365 | TAATTCCAGCACTTC[A/G]GGAGGCCAAGGCAGG | 26091 |
rs57708687 | in-del | -/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68037112 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 26091 |
rs57827703 | in-del | -/A/AA | | | intron-variant | HERC4 | GRCh38.p7 | 10:68000591 | AAAAAAAAAAAAAAA[-/A/AA]TTGTGTGTTGAAATC | 26091 |
rs57830654 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68062781 | ATAATAAATAAAAAA[-/A]TAAAGGACTACCATC | 26091 |
rs57861758 | snp | A/C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67976051 | TTTTTTTTAAGTAAA[A/C/T]TTTGCTGGAAAGCAG | 26091 |
rs57903574 | snp | A/G | 0.143622 | 0.226238 | intron-variant | HERC4 | GRCh38.p7 | 10:67982846 | AAATACCAAACAGGC[A/G]GCAGGGTGCGGTGGC | 26091 |
rs57917056 | snp | C/T | 0.137527 | 0.223271 | intron-variant | HERC4 | GRCh38.p7 | 10:67929663 | GGGACTACTGGTGCA[C/T]GCCACCATAAAGGGC | 26091 |
rs57998331 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HERC4 | GRCh38.p7 | 10:67991416 | TCTAGACTTTCTTAA[A/C]TATTACTTTCATCCA | 26091 |
rs58031306 | in-del | -/AAA | 0.474 | 0.111014 | intron-variant | HERC4 | GRCh38.p7 | 10:67972553 | AAAAAAAAAAAAAAA[-/AAA]GAATTTCTCTGTACT | 26091 |
rs58083532 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67957738 | CCTGCTATGAGACTT[A/C]TAATGAAGAATTAAT | 26091 |
rs58190387 | snp | A/G | 0.137867 | 0.223442 | intron-variant | HERC4 | GRCh38.p7 | 10:68065914 | GCATAGGTTTTTCTC[A/G]CATATAAGGTAATTA | 26091 |
rs58245126 | in-del | -/GG | 0.273318 | 0.24891 | intron-variant | HERC4 | GRCh38.p7 | 10:67998564 | AAAAAAAGGGGGGGG[-/GG]TACAGTACTATCCAG | 26091 |
rs58433144 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927424 | TATATATATATATAT[-/A]TATATATTTTTTTTT | 26091 |
rs58474103 | snp | C/T | 0.165527 | 0.235296 | intron-variant | HERC4 | GRCh38.p7 | 10:67938237 | CACGAGGTCAAGAGA[C/T]TGGGACCATCCTGGC | 26091 |
rs58598572 | snp | A/C | 0.0741063 | 0.177655 | intron-variant | HERC4 | GRCh38.p7 | 10:68041293 | AAATCTTAACACCAA[A/C]TCATTTCAATTTTGA | 26091 |
rs58609957 | in-del | -/TAAA/TAAAA | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67970179 | TAACTCCTGACTAAA[-/TAAA/TAAAA]CTCAAATCCTTACAC | 26091 |
rs58627424 | snp | C/T | 0.144969 | 0.226867 | intron-variant | HERC4 | GRCh38.p7 | 10:68028340 | AAGAGAAGATCACTA[C/T]AAAAATTCATGGATT | 26091 |
rs58692888 | in-del | -/CACACACACA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67946388 | ACACACACACACACA[-/CACACACACA]AGACCCAATGATCTG | 26091 |
rs58694858 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927420 | TATATATATATATAT[-/A]TATATATATATTTTT | 26091 |
rs58740599 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HERC4 | GRCh38.p7 | 10:67970107 | CAAATTCCTCTAGCA[C/T]TACAGGCCTGTAGTG | 26091 |
rs58774283 | snp | A/G | 0.143622 | 0.226238 | intron-variant | HERC4 | GRCh38.p7 | 10:68028017 | ATATATAATAAAAAT[A/G]AGTCAAAGTGTGTCA | 26091 |
rs59036015 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68018278 | TAAAGGAAAAAAAAA[-/A]TCATAAATCATTTCA | 26091 |
rs59039257 | in-del | -/CTTCT | | | intron-variant | HERC4 | GRCh38.p7 | 10:67933367 | ATCACTTCTGATTCT[-/CTTCT]ATCTCTTATGATACA | 26091 |
rs59140367 | snp | G/T | 0.137527 | 0.223271 | intron-variant | HERC4 | GRCh38.p7 | 10:68043115 | TCCTTATAATTAACT[G/T]TCTTTCCATTTATTA | 26091 |
rs59169970 | in-del | -/AAA | | | intron-variant | HERC4 | GRCh38.p7 | 10:68061560 | AAAAAAAAAAAAAAA[-/AAA]GGAATAGGTTTCTGT | 26091 |
rs59263672 | snp | C/T | 0.137527 | 0.223271 | intron-variant | HERC4 | GRCh38.p7 | 10:68031482 | ATGATATTAGGTTGG[C/T]GCAAAATTAATTGCA | 26091 |
rs59318151 | in-del | -/G | 0.252983 | 0.249982 | intron-variant | HERC4 | GRCh38.p7 | 10:67941360 | TACGACTTTACAACT[-/G]TTTTCTCCCAGACAT | 26091 |
rs59415211 | snp | A/T | 0.0741063 | 0.177655 | intron-variant | HERC4 | GRCh38.p7 | 10:68041296 | TCTTAACACCAACTC[A/T]TTTCAATTTTGAAAA | 26091 |
rs59427568 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67972555 | AAAAAAAAAAAAAAA[-/A]GAATTTCTCTGTACT | 26091 |
rs59437368 | in-del | -/GAGA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67963997 | TACCTAGGTCAGAGA[-/GAGA]TGAAGAAAAAAGGAA | 26091 |
rs59754499 | snp | A/C | 0.093417 | 0.194889 | intron-variant | HERC4 | GRCh38.p7 | 10:67998868 | CTCAGCCCCAACGAG[A/C]AGCTGGGACTACAGG | 26091 |
rs59949743 | in-del | -/AACAAT | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68041151 | CCAACCACTAATGTT[-/AACAAT]TAGTAAAAAGTTTAT | 26091 |
rs59977433 | snp | C/T | 0.144296 | 0.226554 | intron-variant | HERC4 | GRCh38.p7 | 10:68021527 | GAATAAGAAATAAAA[C/T]GCTGCGTGCAGTGGC | 26091 |
rs60008145 | snp | G/T | 0.167158 | 0.235875 | intron-variant | HERC4 | GRCh38.p7 | 10:67955540 | ACTTCGGGAGGCCAA[G/T]GAGGGCAGATTACTT | 26091 |
rs60021463 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67983076 | AGGTTGCACTGAGCA[-/A]AAAAAAAAAAAAAAC | 26091 |
rs60065272 | snp | A/C | 0.141934 | 0.225437 | intron-variant | HERC4 | GRCh38.p7 | 10:68043764 | GAGGTTGCAGTGAGC[A/C]GAGATCACACCATTG | 26091 |
rs60169349 | snp | C/T | 0.131381 | 0.220067 | intron-variant | HERC4 | GRCh38.p7 | 10:67980282 | GGGATTACAGACATG[C/T]GCCACCATGCCTGGC | 26091 |
rs60339707 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HERC4 | GRCh38.p7 | 10:67991436 | ACTTTCATCCATTTA[C/T]CCAATGTTATCTGCT | 26091 |
rs60340089 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67929098 | TTATATTTCTATTTT[A/T]ATTCCATTTCTGTCA | 26091 |
rs60420669 | snp | A/G | 0.163236 | 0.234461 | intron-variant | HERC4 | GRCh38.p7 | 10:68028392 | CCATTTTTTGCAGTC[A/G]TTATTTCTTCTCGAT | 26091 |
rs60547325 | snp | A/C | 0.181978 | 0.240568 | intron-variant | HERC4 | GRCh38.p7 | 10:68048724 | GTGCTGCAGAACATC[A/C]AGAAAGCTGGGGAGG | 26091 |
rs60664605 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:68038365 | TACAAAAAAAAAAAA[-/A]TTAAAGGGGTGAAAA | 26091 |
rs60739952 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927422 | TATATATATATATAT[-/A]TATATATATTTTTTT | 26091 |
rs60769846 | in-del | -/T/TT | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67964109 | TTTTTTTTTTTTTTT[-/T/TT]GCTCCTCTTCAATGC | 26091 |
rs60778355 | snp | A/T | 0.132409 | 0.220618 | intron-variant | HERC4 | GRCh38.p7 | 10:68041342 | GGGGAGTAGATTTTT[A/T]AAAAAATGAAAAATT | 26091 |
rs60953059 | snp | C/T | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67983442 | TACTGCTACACTGTT[C/T]ACAATTGCCAAGATT | 26091 |
rs61010062 | snp | C/G | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67999931 | TCCCCTTTCCTACTA[C/G]AATATAATTGAAAAA | 26091 |
rs61012367 | in-del | -/A/AA | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67983805 | AAAAAAAAAAAAAAA[-/A/AA]TACAAAAATTAACTG | 26091 |
rs61130676 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67975984 | AAGGGGTCGGCAAAC[A/T]ACAACCTGTGGGTCA | 26091 |
rs61136290 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927418 | TATATATATATATAT[-/A]TATATATATATATTT | 26091 |
rs61216768 | snp | C/G | 0.0209421 | 0.100162 | intron-variant, nc-transcript-variant | HERC4, POU5F1P5 | GRCh38.p7 | 10:68010248 | TGGCGACAGAAACAG[C/G]GGGAAAGGCACTAAG | 26091 |
rs61219168 | snp | A/C | 0.142272 | 0.225598 | intron-variant | HERC4 | GRCh38.p7 | 10:68022297 | CTGAGGTCGGGAGTT[A/C]GAGACCAGCCTGACC | 26091 |
rs61276590 | in-del | -/A | | | intron-variant | HERC4 | GRCh38.p7 | 10:67927414 | TATATATATATATAT[-/A]TATATATATATATAT | 26091 |
rs61305061 | snp | A/G | 0.0660238 | 0.169271 | intron-variant | HERC4 | GRCh38.p7 | 10:67954557 | TATAAATACATGGGT[A/G]TATACACAGAAGTAA | 26091 |
rs61330513 | snp | C/T | 0.106278 | 0.204558 | intron-variant | HERC4 | GRCh38.p7 | 10:67951551 | GGAAAACTGCTTGTA[C/T]CCTAAACTCCAAATT | 26091 |
rs61386005 | snp | G/T | 0.171057 | 0.237209 | intron-variant | HERC4 | GRCh38.p7 | 10:67972858 | ACAACATTTTTGCTA[G/T]AAATGAGGAAATTTG | 26091 |
rs61429094 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68063404 | TAGTAGAGACGGGGT[C/T]TCACTACACAGGCCA | 26091 |
rs61446193 | snp | C/T | 0.137867 | 0.223442 | intron-variant | HERC4 | GRCh38.p7 | 10:67972952 | GCTACTGCTGTTACA[C/T]AGAAAAATGCCTGTA | 26091 |
rs61552989 | in-del | -/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68003174 | ATACTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 26091 |
rs61670994 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68027742 | ATCCTGGCCAACATG[C/T]TGACACTTCGTCTCT | 26091 |
rs61686051 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67976115 | GAGTTGAGAGTTGAC[A/T]AGTTGCAACAAAAAC | 26091 |
rs61755666 | snp | G/T | 0.00436445 | 0.04651 | synonymous-codon | HERC4 | GRCh38.p7 | 10:67954969 | TCAAATTACCTTGAG[G/T]GGCTTCTTGTAATCT | 26091 |
rs61755667 | snp | A/C/T | 0.00460941 | 0.0477862 | synonymous-codon | HERC4 | GRCh38.p7 | 10:67925146 | CCAAAAAATTTTTAT[A/C/T]GTAGGATGTTCTGCC | 26091 |
rs61755700 | snp | G/T | | | missense | HERC4 | GRCh38.p7 | 10:67922997 | GCGTAGAGTTTCTTT[G/T]TCTGTATATTTTGGA | 26091 |
rs61755701 | snp | G/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68034059 | ACTATGGGCTCCTCC[G/T]GCTGCAACTTGCATG | 26091 |
rs61857498 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67923586 | TTTTTTTTGAGACGA[G/T]TCTTGCTCAGTTGCC | 26091 |
rs61857499 | snp | A/G | 0.029116 | 0.117091 | intron-variant | HERC4 | GRCh38.p7 | 10:67933627 | TTTTTTTAAAACAAG[A/G]ATATCTAGAAGGACC | 26091 |
rs61857512 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67991916 | GGATATTTTTTTTTG[G/T]AGACAAGTTCTCACT | 26091 |
rs61857513 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67996006 | TCTCTATCTGAAAGT[A/G]TCCTTAAAATTCCTC | 26091 |
rs61857514 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68001370 | GAGTGAGACCTTGTA[A/T]TTAAAAAAAAAAAAA | 26091 |
rs61857515 | snp | C/T | | | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68010922 | TTGCAGCAATTCAGT[C/T]ACATTTTCAGGCTTT | 26091 |
rs61857516 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | HERC4 | GRCh38.p7 | 10:68020625 | ATACAAAAAATTAGC[C/T]GGGCGTAGTGGCGGG | 26091 |
rs61857517 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68026670 | AAAAAGGTGAAACCC[C/T]GTCACTACTAAAAAT | 26091 |
rs61857518 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68030112 | GGCAAGGCACATTTG[G/T]TCTGGCTATTAATTT | 26091 |
rs61857519 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68034594 | AAATTTTAACACTAG[C/T]CCAAACCTCTCCTGA | 26091 |
rs61857520 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:68046131 | ATGACACACACTGTT[A/C]CAAAAAAAAAAAAGA | 26091 |
rs61857521 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68046764 | TTGAACCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 26091 |
rs61857522 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68047198 | TTTATTGACTTCTTA[A/G]GGAAAAAAAAAAAAA | 26091 |
rs61857523 | snp | A/C/T | 0.0785661 | 0.182154 | intron-variant | HERC4 | GRCh38.p7 | 10:68055748 | TACTTAGGGGCATTA[A/C/T]AATATCCTTTTTTTT | 26091 |
rs61857524 | snp | C/G | | | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68076980 | AAAATACAAAATTAG[C/G]CGGGCGTGGTGGTGC | 26091 |
rs63560661 | snp | A/C | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67962224 | AAAGTTTAAATAAGC[A/C]AAAAAAAAAAAGCCT | 26091 |
rs67602944 | snp | A/C | 0.438806 | 0.163867 | intron-variant | HERC4 | GRCh38.p7 | 10:67959644 | TTGACAGAAAAAAAA[A/C]CAGTAAAACATAAGG | 26091 |
rs67630220 | multinucleotide-polymorphism | AACAT/CAAAA | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67945821 | AAACTCAAATCAAAA[AACAT/CAAAA]ACGACAGATACACGA | 26091 |
rs67767919 | multinucleotide-polymorphism | GTG/TTT | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68003342 | AATTTTTTTTTTTTT[GTG/TTT]TGTATTTTTAGTAGA | 26091 |
rs67804458 | in-del | -/TACACACA | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67974121 | ACACACACACACACA[-/TACACACA]GGGTCAGGAAAACAA | 26091 |
rs71006191 | in-del | -/A | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67952910 | GTCTCAAAAAAAAAG[-/A]AAAAAAAAAAGACAC | 26091 |
rs71006193 | in-del | -/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68003367 | TTAGTAGAGATGGGG[-/G]TTTCACTGTGTTAGC | 26091 |
rs71006198 | in-del | -/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68051362 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 26091 |
rs71006199 | in-del | -/TATATATCATAATATTATATATTATAATAT | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68059845 | TATATATTATAATAT[lengthTooLong]ATTATATATCATAAT | 26091 |
rs71468899 | snp | A/C | 0.444444 | 0.157135 | intron-variant | HERC4 | GRCh38.p7 | 10:67926432 | AAAAAAAAAAAAAAA[A/C]AAAAAAATTAGTACT | 26091 |
rs71468900 | in-del | -/TA | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67974072 | AAAAAAAAATTACTG[-/TA]TACACACACACACAC | 26091 |
rs71470503 | in-del | -/AAAAA | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68061880 | AGCGAGACTCCATTT[-/AAAAA]AAAAAAAAAAAAAAA | 26091 |
rs71475220 | snp | A/C | 0.201727 | 0.245295 | intron-variant | HERC4 | GRCh38.p7 | 10:67924745 | GTCTTGGAATCAATC[A/C]CCCATGTATGCCAAA | 26091 |
rs71475222 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67974707 | TCGTAAAAAGAATTG[G/T]TTATATAATTTTCAT | 26091 |
rs71475223 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67986355 | AACTTACATATATTG[G/T]ATTATTTATTTTTTT | 26091 |
rs71475224 | snp | A/T | 0.190833 | 0.242898 | intron-variant | HERC4 | GRCh38.p7 | 10:68005684 | TTTCCTTTTTTTTTT[A/T]AATTTTCTGTGCATC | 26091 |
rs71475225 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68008899 | TGCAAGTCACACAAA[A/T]TTTTGGTTTCATAGT | 26091 |
rs71865695 | in-del | -/T/TT | | | intron-variant | HERC4 | GRCh38.p7 | 10:67964108 | CAGCTACCACTCCAT[-/T/TT]TTTTTTTTTTTTTTT | 26091 |
rs71963502 | in-del | -/CA | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059519 | TATAATATTATATAT[-/CA]TAATAATATTATATA | 26091 |
rs72138572 | in-del | -/AAAC/TAAA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67970176 | GCTTAACTCCTGACT[-/AAAC/TAAA]AAACTCAAATCCTTA | 26091 |
rs72232670 | in-del | -/TTCTC | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:67933363 | TACAATCACTTCTGA[-/TTCTC]TTCTATCTCTTATGA | 26091 |
rs72449735 | in-del | -/C | 0.26326 | 0.249648 | intron-variant | HERC4 | GRCh38.p7 | 10:68046992 | ACAAACAAAAAAAAA[-/C]ATGAAGAATTTTGGA | 26091 |
rs72512850 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67996314 | AGACCTTGAAATAGA[-/C]ACCCCCCCTGCCCCA | 26091 |
rs72512851 | in-del | -/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:68021053 | ATAGCCAAAAACTCC[-/C]CMAATATGGGGAAAG | 26091 |
rs72637093 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67996315 | GACCTTGAAATAGAC[A/C]CCCCCCCTGCCCCAC | 26091 |
rs72795403 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | HERC4 | GRCh38.p7 | 10:68066036 | CCATGAGCTCATTAA[C/T]ATAGTTTCCTCATTA | 26091 |
rs72808646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:67982756 | GCTGAAACAATTCTA[C/T]AGAAAAAAATGCAAT | 26091 |
rs72808655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68013379 | TATCTCCAAGGTATG[C/T]CTGAATTATATAGCT | 26091 |
rs72808658 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68030510 | TTGGTCCCTTTCTTA[C/T]AGAAAGCTGTTCCAT | 26091 |
rs72808660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68047183 | ATAACATCCCCAGTT[C/T]TTATTGACTTCTTAG | 26091 |
rs72808661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68054870 | AAATTATTGTTTAAA[G/T]AAAACAAAGTGCAAC | 26091 |
rs73261363 | snp | C/G | 0.0755793 | 0.179102 | utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:67922763 | TAATATTAACAGTTT[C/G]TTCATTTTCCTTTAA | 26091 |
rs73261366 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | HERC4 | GRCh38.p7 | 10:67926769 | TGTGGAGCTCACCGT[C/T]TAGTAAGAGGCGTTC | 26091 |
rs73261373 | snp | C/T | 0.163892 | 0.234703 | intron-variant | HERC4 | GRCh38.p7 | 10:67930516 | AAAGTGACTATACCA[C/T]TTTGTATCCCCATCG | 26091 |
rs73261376 | snp | A/T | 0.142609 | 0.225759 | intron-variant | HERC4 | GRCh38.p7 | 10:67935782 | AAGAGTTCTAGCATT[A/T]CCCCAAACACCATGC | 26091 |
rs73261377 | snp | A/G | 0.164546 | 0.234942 | intron-variant | HERC4 | GRCh38.p7 | 10:67935869 | CCAGCTGGCTTCGTG[A/G]CTCCTCTTTTCCATC | 26091 |
rs73261379 | snp | C/T | 0.163892 | 0.234703 | intron-variant | HERC4 | GRCh38.p7 | 10:67937615 | TAATTTTATGGTCAC[C/T]TTATTCTAACAGGAA | 26091 |
rs73261381 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67938045 | TTTTTGGCAAATTTT[A/G]TGACAGCAGAATATG | 26091 |
rs73263204 | snp | C/T | 0.137527 | 0.223271 | intron-variant, downstream-variant-500B | HERC4 | GRCh38.p7 | 10:67966186 | ATTTCGTCATGTTGC[C/T]GAGGCTGGTCTTGAA | 26091 |
rs73263214 | snp | C/T | 0.137187 | 0.223099 | intron-variant | HERC4 | GRCh38.p7 | 10:67975247 | AAATAAAACCTATCA[C/T]TAAAGTGGACTTCAT | 26091 |
rs73263217 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | HERC4 | GRCh38.p7 | 10:67975844 | CACTGTTTTGATTGC[C/T]TTATATCTGTGGCCA | 26091 |
rs73263222 | snp | A/G | 0.137527 | 0.223271 | intron-variant | HERC4 | GRCh38.p7 | 10:67978459 | CTGCAGTACAACAGA[A/G]CACCAGGTAGACGTC | 26091 |
rs73263241 | snp | A/G | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67986795 | GTAGGAAGCAACACA[A/G]AGGGGTTAGAAATAT | 26091 |
rs73263244 | snp | C/G | 0.143959 | 0.226396 | intron-variant | HERC4 | GRCh38.p7 | 10:67997203 | AGTTAACTCAATTTA[C/G]AAGGACCTGCTCCCT | 26091 |
rs73263262 | snp | A/G | 0.144632 | 0.226711 | intron-variant | HERC4 | GRCh38.p7 | 10:68015433 | CTAGGTTTTGGAGTC[A/G]TTCTGTTTAGCGACA | 26091 |
rs73263264 | snp | C/T | 0.141596 | 0.225274 | intron-variant | HERC4 | GRCh38.p7 | 10:68021318 | GCAAACCTGGTTCAA[C/T]ATATGAAAATTAATA | 26091 |
rs73263271 | snp | A/G | 0.144296 | 0.226554 | intron-variant | HERC4 | GRCh38.p7 | 10:68025177 | AGGCTGCAATAAGCC[A/G]TAATTGTGGTACTCC | 26091 |
rs73263298 | snp | C/G | 0.136166 | 0.22258 | intron-variant | HERC4 | GRCh38.p7 | 10:68054668 | TTCTGACTTTTTAAA[C/G]ATAAAGATATTAATC | 26091 |
rs73263301 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC4 | GRCh38.p7 | 10:68056526 | TGAATTCCATGGGCT[A/G]TACTTGGTAGTACAC | 26091 |
rs73265217 | snp | A/G | 0.137867 | 0.223442 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68075278 | GGGAGAGTTGGGGAA[A/G]AGACTGGGTAGGAGA | 26091 |
rs74145828 | snp | A/G | 0.136166 | 0.22258 | intron-variant | HERC4 | GRCh38.p7 | 10:67957720 | CTGCCCTGACTCAGA[A/G]CCCCTGCTATGAGAC | 26091 |
rs74145829 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | HERC4 | GRCh38.p7 | 10:67969379 | ATAGTATGAAACCCC[A/G]CAGAGTCCCAGGCAG | 26091 |
rs74145833 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:67993835 | CCAAAAATATTGCTT[A/G]GCTAGTCCATAGTCT | 26091 |
rs74145836 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:68035717 | ACTCTAGCCGTATTG[C/T]CTTCCTTTATATTCT | 26091 |
rs74145837 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | HERC4 | GRCh38.p7 | 10:68071749 | CATTTACTTTGAGTT[C/G]TGCAAGAATTAAAAA | 26091 |
rs74397981 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HERC4 | GRCh38.p7 | 10:67944039 | CTCTGCACTGAAGGG[A/G]AGAACACAAGCTTCG | 26091 |
rs74399112 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67968390 | TCCTTTTTTTTTTTT[G/T]GAGACAAAGTCTCGC | 26091 |
rs74468943 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67968391 | CCTTTTTTTTTTTTT[G/T]AGACAAAGTCTCGCT | 26091 |
rs74481077 | in-del | -/AA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67962234 | TAAGCAAAAAAAAAA[-/AA]GCCTATAAAAATTTA | 26091 |
rs74526058 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HERC4 | GRCh38.p7 | 10:67957250 | TATGTTAATTGCAAA[C/T]CTCAGTGAATGAGGT | 26091 |
rs74541537 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | HERC4 | GRCh38.p7 | 10:67960120 | GCTTCCAGAAGAGCT[A/G]GGAACTAGAGGTCAC | 26091 |
rs74541925 | snp | G/T | 0.0678174 | 0.1712 | downstream-variant-500B | HERC4 | GRCh38.p7 | 10:67921661 | AAAGCACCCAATAGC[G/T]GTCATAGTCTTATTT | 26091 |
rs74570566 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67935162 | ATTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 26091 |
rs74621981 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | HERC4 | GRCh38.p7 | 10:68045361 | AAGGAAATAATCTGA[A/G]TTAGCAATTTCTGAA | 26091 |
rs74636031 | snp | A/C | 0.067446 | 0.170804 | intron-variant | HERC4 | GRCh38.p7 | 10:67996606 | CTTAAAATTGAGAAA[A/C]TTAAAAAATAGTTTT | 26091 |
rs74741499 | snp | C/T | 0.0185938 | 0.0946107 | downstream-variant-500B | HERC4 | GRCh38.p7 | 10:67921515 | GTTTTAGTGCTTCTA[C/T]CTATAGAAGAGTTCT | 26091 |
rs74761671 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | HERC4 | GRCh38.p7 | 10:68018606 | GTAAGTTATTAATAA[C/G]AGTTTAGCAAGGTGG | 26091 |
rs74790906 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68028263 | TTAAAAAAAAAAAAA[A/T]GAGTGTTGTCCTAGC | 26091 |
rs74858015 | snp | A/C | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68038353 | ACAAGAGCTAGATAC[A/C]AAAAAAAAAAAATTA | 26091 |
rs74909384 | in-del | -/TT | | | intron-variant | HERC4 | GRCh38.p7 | 10:67976042 | CTGTTTTTTTTTTTT[-/TT]AAGTAAATTTTGCTG | 26091 |
rs74924746 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | HERC4 | GRCh38.p7 | 10:68017885 | ATAAAAGCTATCTCA[C/T]AGCCACTAAAGAAAT | 26091 |
rs74955033 | snp | A/C | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67983075 | GGAGGTTGCACTGAG[A/C]AAAAAAAAAAAAAAA | 26091 |
rs74977303 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | HERC4 | GRCh38.p7 | 10:67965535 | CCAGTCCAGACCCAA[C/G]TACACTAGGGAAGGA | 26091 |
rs75028881 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | HERC4 | GRCh38.p7 | 10:68042873 | AAAAACTATGTATAC[A/G]TTACAACAAATCAGA | 26091 |
rs75065688 | snp | C/G/T | 0.067446 | 0.170804 | intron-variant | HERC4 | GRCh38.p7 | 10:67981532 | GCACTATAGACCAAA[C/G/T]GGACCAAACACATAT | 26091 |
rs75075869 | in-del | -/AA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67946259 | TGTCCAAAAAAAAAA[-/AA]GATGCAAGAGTAACT | 26091 |
rs75081639 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67970180 | TAACTCCTGACTAAA[C/T]TCAAATCCTTACACT | 26091 |
rs75210577 | in-del | -/GGG | | | intron-variant | HERC4 | GRCh38.p7 | 10:67998571 | AAAAAAAAGGGGGGG[-/GGG]TACAGTACTATCCAG | 26091 |
rs75227577 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HERC4 | GRCh38.p7 | 10:67953809 | TCTCTATACAGAAGT[A/G]TCCAAGCTAATAAAT | 26091 |
rs75262001 | snp | A/T | 0.067446 | 0.170804 | intron-variant | HERC4 | GRCh38.p7 | 10:68036029 | GCTCTAAAAAATGTT[A/T]AGCGGCTGGGCACAG | 26091 |
rs75331449 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | HERC4, POU5F1P5 | GRCh38.p7 | 10:68010028 | CAAGAGCATCACCGA[A/C]CTTCACCTTCCCTCC | 26091 |
rs75333151 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:67960939 | CCACTTCTTTCAAGT[C/T]ACTTGTCTGAACCTC | 26091 |
rs75340014 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:68035485 | TTACCAATTACTGGT[A/G]AGTCCTTCAAGAAAT | 26091 |
rs75365066 | snp | A/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68007716 | ACTTTTTTTTTTTTT[A/T]AAGAGACAGAGTCTC | 26091 |
rs75365849 | snp | C/T | 3.30715e-05 | 0.00406628 | intron-variant, missense | HERC4 | GRCh38.p7 | 10:67940948 | ACTAACCTCCCAACA[C/T]CAGGCATTAGTTCTT | 26091 |
rs75368843 | snp | C/T | 0.170733 | 0.237101 | intron-variant | HERC4 | GRCh38.p7 | 10:67996710 | TTTTGACTGGCCAGG[C/T]GCGGTGGCTCACACT | 26091 |
rs75403123 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68046986 | AAACAAACAAACAAA[A/C]AAAAACATGAAGAAT | 26091 |
rs75434429 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67938438 | GCAAGATTCTGTCTC[A/C]AAAAAAAAGAAAAAA | 26091 |
rs75461745 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | HERC4 | GRCh38.p7 | 10:67986185 | AAAGAGATGTTTAAG[A/G]AAGTCATACCAGTAT | 26091 |
rs75471445 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HERC4 | GRCh38.p7 | 10:68065687 | CAAAAGAGTGGAACC[A/C]TGTCTCTATAAAAAA | 26091 |
rs75480467 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67935164 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 26091 |
rs75527079 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67956844 | ACATCAAAGAAACAA[A/T]TAAAAAAAAAAACCC | 26091 |
rs75541882 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68051361 | TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTCG | 26091 |
rs75572869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68049017 | AACAAAACACATGCA[C/T]TCACCCTTCAGACCT | 26091 |
rs75616741 | snp | A/G | 0.263535 | 0.249633 | intron-variant | HERC4 | GRCh38.p7 | 10:68066486 | GGTTCCAAGTACTTT[A/G]AAGAAGTTTCCCTTT | 26091 |
rs75635737 | snp | A/C | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67984303 | TGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 26091 |
rs75635906 | snp | A/C | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68046133 | GACACACACTGTTCC[A/C]AAAAAAAAAAAGAAA | 26091 |
rs75724917 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:68065646 | GGGAGTCTGAGGTGC[A/G]AGGATCACTTCGAGA | 26091 |
rs75749461 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HERC4 | GRCh38.p7 | 10:67950844 | GAACTACTGACTCTC[C/T]GGAAGCAAGAAGTAC | 26091 |
rs75763220 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HERC4 | GRCh38.p7 | 10:67962887 | CAAGGTAGCCAGCAA[C/T]AATAATCACCATTTT | 26091 |
rs75793095 | snp | A/T | 0.0505692 | 0.150756 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68075225 | TGGAGCGGGCGGGGA[A/T]GAACGGGAGGCAAGC | 26091 |
rs75935254 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | HERC4 | GRCh38.p7 | 10:67960814 | AGCTCCCTGGTTTTC[C/T]CAGTTCAAACTTGGG | 26091 |
rs75993472 | snp | C/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67941904 | CAGGTGATCTGCTCA[C/G]GTCAGCCTCCCAAAG | 26091 |
rs76014573 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:67974866 | AAGGGAAGCTAAAAT[C/T]TTCACTACAATGCAG | 26091 |
rs76030850 | snp | C/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68017850 | AAAAATTAACATTCA[C/G]ATAACTGACTCAAGA | 26091 |
rs76054043 | snp | A/C | 0.481087 | 0.0953875 | intron-variant | HERC4 | GRCh38.p7 | 10:67945819 | ACTCAAATCAAAAAA[A/C]ATACGACAGATACAC | 26091 |
rs76068815 | in-del | -/TTA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67923708 | GAGCACAGTCACCAA[-/TTA]GCCCAGGGCTAATTT | 26091 |
rs76075985 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68007718 | TTTTTTTTTTTTTTA[A/G]GAGACAGAGTCTCAC | 26091 |
rs76109593 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68057625 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAGT | 26091 |
rs76113304 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:68040303 | AGTATATTCTTCTGC[A/G]TCATTACTGTGTTAA | 26091 |
rs76120841 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68064845 | GGAGTGGTGGCACAC[G/T]TCTGTAATCCCAGCT | 26091 |
rs76188211 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68012847 | TAAGCTTTAGTAATT[C/T]TCGCAATATTTCAAT | 26091 |
rs76194386 | in-del | -/A | 0.18134 | 0.240387 | intron-variant | HERC4 | GRCh38.p7 | 10:68058083 | TGTGCTTCTCACAAG[-/A]AAAAAAAAGGCATCT | 26091 |
rs76231628 | snp | A/C | 0.031825 | 0.122064 | intron-variant | HERC4 | GRCh38.p7 | 10:67933256 | AAAATTTACTTTAAC[A/C]AATGCCTAAGAGAGG | 26091 |
rs76238113 | snp | C/T | 0.114387 | 0.210022 | intron-variant | HERC4 | GRCh38.p7 | 10:67958575 | GAAAGTATTATAATG[C/T]TCCCAAGTGTTAAAA | 26091 |
rs76358545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68022204 | CAATGCTACCCAAAA[A/G]AATGTACAGACTCGG | 26091 |
rs76376861 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:68023825 | AAAATAAATCAACTT[C/G]AGATAACTTACAGAC | 26091 |
rs76408389 | snp | A/C | 0.253544 | 0.249975 | intron-variant | HERC4 | GRCh38.p7 | 10:67943890 | CCTGTAGAGTGGGAA[A/C]AATTTTGCCTTGTGG | 26091 |
rs76453667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68060794 | CCTATTAGAGAGCCT[A/G]GTTATGAAATCTATA | 26091 |
rs76467714 | snp | A/G | 0.162581 | 0.234218 | intron-variant | HERC4 | GRCh38.p7 | 10:67949494 | CCCCAAAACAAAAAA[A/G]CAGTAACAAACAAAA | 26091 |
rs76488952 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:67999169 | GTATCTCAAGATTTC[A/G]TTTTTGTCTATAAAT | 26091 |
rs76556342 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68053513 | CTCCCTATTTTGCCC[A/G]GGCTAGTCTTGAACT | 26091 |
rs76581482 | snp | C/T | 0.375 | 0.216506 | intron-variant | HERC4 | GRCh38.p7 | 10:68059494 | TATTATATATTATAA[C/T]ATTATATATTATAAT | 26091 |
rs76604446 | snp | A/C | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68038352 | AACAAGAGCTAGATA[A/C]AAAAAAAAAAAAATT | 26091 |
rs76619373 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68028261 | AGTTAAAAAAAAAAA[A/T]ATGAGTGTTGTCCTA | 26091 |
rs76710968 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67964091 | TCCAGCTACCACTCC[A/T]TTTTTTTTTTTTTTT | 26091 |
rs76735234 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68028262 | GTTAAAAAAAAAAAA[A/T]TGAGTGTTGTCCTAG | 26091 |
rs76778876 | snp | A/G | 0.114036 | 0.209795 | intron-variant | HERC4 | GRCh38.p7 | 10:68020960 | CTAGGGGAACCATAG[A/G]ATACCATTAAGCAGA | 26091 |
rs76789660 | snp | A/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67993538 | CTAAAAAAAAAAAAA[A/T]TTATTCTTAAAAAGA | 26091 |
rs76818127 | snp | C/T | 0.067446 | 0.170804 | intron-variant | HERC4 | GRCh38.p7 | 10:67961255 | TCATCATTCTGCAGA[C/T]CAGAAAGGTTCACTT | 26091 |
rs76919885 | snp | C/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68041106 | TAGGCAGAAATCAGG[C/G]ATTGTTAGTTATGTT | 26091 |
rs76924291 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67974348 | AGAAGAAAAACCACC[A/T]AAGAAACAAATAAAG | 26091 |
rs76985093 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:67988047 | GGTATACCTACCAAC[C/T]GTCAGGGATGAAAAT | 26091 |
rs77042467 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67923579 | CATTCTTTTTTTTTT[G/T]AGACGAGTCTTGCTC | 26091 |
rs77099977 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68027226 | GAACATTCATTTTTC[C/T]TTTTTTATCACAGAA | 26091 |
rs77138936 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68060931 | TCCTAAAAAAAAAAA[A/G]GTCACAAATGTCTTC | 26091 |
rs77230733 | in-del | -/AT | | | intron-variant | HERC4 | GRCh38.p7 | 10:68036482 | CAAAAGAGGAGTTGG[-/AT]CAAAACAACAAAGAA | 26091 |
rs77290846 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | HERC4 | GRCh38.p7 | 10:68012998 | AACCACATCCATATA[A/G]TAAGAACACAGGCAT | 26091 |
rs77299457 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:67941598 | ATATTTTTAATACAC[C/T]GTATTTAAGATTTTA | 26091 |
rs77309034 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075630 | TTGTCTTTGTGCTCA[G/T]GGATGCTAGCTAGTC | 26091 |
rs77355571 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68029179 | AGACCCCCATCTCAG[A/G]AAAAAAAAAGTTACA | 26091 |
rs77383689 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67949774 | GCTCACGCCAGCACT[C/T]TGAGTGGCTGAGGCA | 26091 |
rs77386778 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68001373 | TGAGACCTTGTATTT[A/T]AAAAAAAAAAAAATT | 26091 |
rs77400152 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:67942994 | TACATATGTGCTCAT[A/G]AAATATCTCTCCAGG | 26091 |
rs77493845 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:68047243 | ATGACAAGTGGGTAA[A/G]AGATGTGAACCAAAA | 26091 |
rs77516081 | snp | A/G | 0.32 | 0.24 | intron-variant | HERC4 | GRCh38.p7 | 10:67998456 | GGAGGCTGAGGCAGG[A/G]GAATTGCTTGAATCC | 26091 |
rs77831275 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:67968218 | AAGGAATCCAGAGGA[C/T]GAAGCCCCAAAATCT | 26091 |
rs77839284 | snp | A/G | 0.182933 | 0.240836 | intron-variant | HERC4 | GRCh38.p7 | 10:68037188 | CAACTTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 26091 |
rs77918149 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HERC4 | GRCh38.p7 | 10:68073286 | CTACATGGTAAACAT[C/T]AAATATACTTTATAA | 26091 |
rs78006954 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HERC4 | GRCh38.p7 | 10:68061121 | TAGCTCTTGCCTACA[C/T]TGCCCGCATATATAC | 26091 |
rs78026931 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HERC4 | GRCh38.p7 | 10:67994346 | TCCCTACAAGATGGT[C/T]GACTAATCTACAGTA | 26091 |
rs78073931 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68042035 | TTTTTTTTATTTTTT[G/T]AGATGGAGTCTCGCT | 26091 |
rs78113937 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | HERC4 | GRCh38.p7 | 10:67936611 | ATGCATTCTTCCCAC[A/C/G]TGACAACTGCTACTC | 26091 |
rs78135151 | snp | A/T | 0.00017113 | 0.00924856 | intron-variant | HERC4 | GRCh38.p7 | 10:67956846 | ATCAAAGAAACAATT[A/T]AAAAAAAAAACCCTC | 26091 |
rs78162501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68055482 | AGTTCATACCCCTTT[A/T]ATATATTTATACAGA | 26091 |
rs78197922 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68046143 | GTTCCAAAAAAAAAA[A/G]AGAAAAAATACTTAG | 26091 |
rs78270106 | snp | A/C | 0.0439338 | 0.141551 | intron-variant | HERC4 | GRCh38.p7 | 10:67996031 | TTCCTCTCCGCTGGG[A/C]ACAGTAGCTCATACC | 26091 |
rs78271535 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | HERC4 | GRCh38.p7 | 10:68049316 | TATTTTTTGTGTAAG[A/G]GGAAGAAGAAAACAT | 26091 |
rs78378081 | in-del | -/GA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67998551 | CACTCCACCTCAATT[-/GA]AAAAAAAAAAAGGGG | 26091 |
rs78421304 | snp | C/T | 0.029116 | 0.117091 | intron-variant | HERC4 | GRCh38.p7 | 10:68017050 | TTGGGCTGTATATTA[C/T]ATTCCCCATACCTTA | 26091 |
rs78543319 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HERC4 | GRCh38.p7 | 10:67963984 | GAAGAGTTTGAGAAG[C/T]TTTACCTAGGTCAGA | 26091 |
rs78568733 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HERC4 | GRCh38.p7 | 10:68068906 | CGGACCATGATACCT[A/G]CCTTAGCTACATACA | 26091 |
rs78639655 | snp | A/G | 0.170084 | 0.236883 | intron-variant | HERC4 | GRCh38.p7 | 10:67999983 | CTTATCTGAAGTGTT[A/G]TATTTGAGAACAACG | 26091 |
rs78677821 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:67962223 | GAAAGTTTAAATAAG[A/C]AAAAAAAAAAAAGCC | 26091 |
rs78679383 | snp | A/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68053324 | ACTTTTTTTTTTTTT[A/T]AGACCAGGTCTCTCT | 26091 |
rs78721245 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | HERC4 | GRCh38.p7 | 10:67956466 | ACATCTTCTTCCTAA[C/T]GAGATCAAATGCTTC | 26091 |
rs78871215 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | HERC4, POU5F1P5 | GRCh38.p7 | 10:68009598 | TGGCTACTGACTGAT[C/T]AGGGTGGTAATTGCT | 26091 |
rs78946347 | snp | A/T | 0.00337902 | 0.0409645 | intron-variant | HERC4 | GRCh38.p7 | 10:68032755 | TGATGAGTAATAATA[A/T]AGAAGTTTTAGAAGT | 26091 |
rs78991018 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | HERC4, POU5F1P5 | GRCh38.p7 | 10:68009466 | TATCTTAAAAAAAAA[A/T]TCCATATACCTTAAT | 26091 |
rs79024650 | snp | A/C | 0.181978 | 0.240568 | intron-variant | HERC4 | GRCh38.p7 | 10:68052013 | ATATAAAAAGGGTGA[A/C]AAAAAAGTATCATTG | 26091 |
rs79041175 | snp | G/T | 0.170733 | 0.237101 | intron-variant | HERC4 | GRCh38.p7 | 10:67995628 | ATATTAACCTTAGGT[G/T]GTAATTGCTACAAAT | 26091 |
rs79041829 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | HERC4 | GRCh38.p7 | 10:68060207 | AATCAGCATTATAAG[C/G]TGTAAATAATGTTCT | 26091 |
rs79046781 | snp | C/G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67942722 | CTCCATGTTGGTCAG[C/G/T]CTGGTCTCGAACCCC | 26091 |
rs79052195 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68053325 | CTTTTTTTTTTTTTT[A/G]GACCAGGTCTCTCTG | 26091 |
rs79073066 | snp | A/C | | | intron-variant | HERC4 | GRCh38.p7 | 10:68053512 | TCTCCCTATTTTGCC[A/C]AGGCTAGTCTTGAAC | 26091 |
rs79082399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68030822 | CTTGAAAAAAATGTG[A/G]CATCTTTATGGAAGT | 26091 |
rs79117523 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67923578 | TCATTCTTTTTTTTT[G/T]GAGACGAGTCTTGCT | 26091 |
rs79127437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:67951671 | TTCATATGATTGCGT[C/T]TAGAGCTAAGGTAGG | 26091 |
rs79144922 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67993879 | TATTCCCATTCCTTA[A/G]TTGACTAATTCTTCA | 26091 |
rs79148261 | snp | C/T | 0.00401247 | 0.0446109 | intron-variant, synonymous-codon, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68039479 | GACACACATGATTTT[C/T]GGGAAGCAGCTTCAG | 26091 |
rs79191660 | in-del | -/AA | | | intron-variant | HERC4 | GRCh38.p7 | 10:67991041 | GAAAAGAAAAAAAAA[-/AA]TAGAATAAAAATTTA | 26091 |
rs79216096 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68023017 | ATTATAAAAAAAAAA[A/G]GAAAAAGGCAAAATG | 26091 |
rs79246310 | snp | A/C | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68064972 | CAAGGCTCCATCTCA[A/C]AAAAAAAAAAAAATC | 26091 |
rs79343027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68041907 | TGTTTCAGTTATATC[C/T]TATTGTTAATTTCAC | 26091 |
rs79362506 | snp | C/G | 0.171057 | 0.237209 | intron-variant | HERC4 | GRCh38.p7 | 10:68020119 | GCTAAGAAAAGACCT[C/G]ATTTTTATACCTCAG | 26091 |
rs79376597 | snp | A/G | 0.170733 | 0.237101 | intron-variant | HERC4 | GRCh38.p7 | 10:67978434 | TTTTGTGGTTTGAGG[A/G]CCAGCTCAGCTGCAG | 26091 |
rs79448633 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67938458 | AAAAGAAAAAAAAAA[A/G]GAAAAGAAAAGGGAA | 26091 |
rs79449363 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67990457 | AATACACTTTCAAAG[A/G]AAAAAAAAAAAAAGG | 26091 |
rs79462701 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | HERC4 | GRCh38.p7 | 10:68050335 | TGTGAATATATATTG[C/T]CTTTTCAAAACAAAC | 26091 |
rs79471652 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HERC4 | GRCh38.p7 | 10:68060882 | TATCAATTGTGGGAA[A/G]CAATTTAAGATCTAC | 26091 |
rs79496251 | snp | A/G | 0.067446 | 0.170804 | intron-variant | HERC4 | GRCh38.p7 | 10:67967792 | GTTTATAGGAAATAC[A/G]AGGGATAGAGGAACA | 26091 |
rs79506902 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HERC4 | GRCh38.p7 | 10:67954119 | GGTCACTGTTGTAAT[G/T]ACTTAAACTCTGCCG | 26091 |
rs79532273 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67945620 | CTAAAACATGAACCA[A/T]TAAAAAATAATAACT | 26091 |
rs79539200 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HERC4 | GRCh38.p7 | 10:67999549 | AGAGATCTCTCTTAC[A/G]TAACTTTCAAAACGT | 26091 |
rs79564897 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68000167 | CAGCCAATAAGTCAT[C/G]TGAAGGAACAAAGTT | 26091 |
rs79600181 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68051363 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 26091 |
rs79757490 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HERC4 | GRCh38.p7 | 10:68050268 | ATAGCGTGGTCAAAT[A/G]TAAGAGCCAAGCTTC | 26091 |
rs79760944 | snp | A/G | 0.170408 | 0.236992 | intron-variant | HERC4 | GRCh38.p7 | 10:67941195 | CTCATATACAATTTT[A/G]AAGATAGAGAAAAAA | 26091 |
rs79804696 | snp | A/C | 0.170408 | 0.236992 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68070315 | AAAACATTATTTAAA[A/C]AACATCTTAGGCCAG | 26091 |
rs79947124 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:67953477 | CTGTCATAGTAAGTA[C/T]ACAAGGTAGCAAGGA | 26091 |
rs79977500 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | HERC4 | GRCh38.p7 | 10:68057769 | TAGAGTGCAGTGGTG[C/T]AATCACTGCAACCAC | 26091 |
rs80000001 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HERC4 | GRCh38.p7 | 10:68072072 | ATTATTGTTACAGTT[A/C]AAATAAACAGTAAGT | 26091 |
rs80022024 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68060932 | CCTAAAAAAAAAAAA[G/T]TCACAAATGTCTTCT | 26091 |
rs80039640 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | HERC4 | GRCh38.p7 | 10:67957252 | TGTTAATTGCAAATC[C/T]CAGTGAATGAGGTTG | 26091 |
rs80052502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68052204 | ACAGATGAAACATAT[C/T]CACTTTGTAGATAAC | 26091 |
rs80102766 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:67983697 | GAGGCTGAGGCAGGA[A/G]AACAGCATGAACCCA | 26091 |
rs80117551 | snp | C/T | 0.16976 | 0.236773 | intron-variant, upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075071 | GTCAGCCAGTGGCGA[C/T]GATCACCAGGGCACC | 26091 |
rs80123155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:67947191 | GTTCTCTACAACATA[C/T]GGATGGACCATATAT | 26091 |
rs80196465 | snp | C/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67998469 | GGAGAATTGCTTGAA[C/T]CCGGGAGGCAGAGGT | 26091 |
rs80220606 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67983060 | TTGAACCCAGGAAGC[A/G]GAGGTTGCACTGAGC | 26091 |
rs80271165 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:67924521 | TTGTGTATCTAAACA[G/T]AGAAAAGGTACAGTA | 26091 |
rs80298796 | in-del | -/TG | | | intron-variant | HERC4 | GRCh38.p7 | 10:67995429 | TATTTACTGTCCTCT[-/TG]CTTTTCAAATTTGCA | 26091 |
rs111123308 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68059509 | CATTATATATTATAA[C/T]ATTATATATCATAAT | 26091 |
rs111209619 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68059696 | CATAATATTATATAT[C/T]ATAATATTATATATC | 26091 |
rs111242809 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68044744 | AACTATTCAACAAAT[A/G]TGTTCCAAACGTAAT | 26091 |
rs111273207 | snp | A/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68059908 | TATTATATATTATAT[A/T]ATATTATATATCATA | 26091 |
rs111288689 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:68008063 | TACTGCCTTGGTGAA[C/T]TTGGGTAAGATCTGG | 26091 |
rs111316409 | snp | A/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67923292 | AAGACAAGTTTTTTG[A/T]GACACATTCTAATTG | 26091 |
rs111395339 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67997706 | TGCTTTTCAAATTTG[C/T]ATTTCTTTGATACTA | 26091 |
rs111396531 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | HERC4 | GRCh38.p7 | 10:68019663 | TTTCCAAGAGAAGAG[A/C/T]TGGATGGCAAATTCT | 26091 |
rs111397100 | snp | C/T | 0.030278 | 0.119257 | intron-variant | HERC4 | GRCh38.p7 | 10:68025159 | CTTGAGCCCAGGAGA[C/T]TGAGGCTGCAATAAG | 26091 |
rs111403385 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:67955815 | AGGAATGATCTGGCT[A/T]AGGAAGCATTACACA | 26091 |
rs111457740 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HERC4 | GRCh38.p7 | 10:67944803 | AAAAATGCAACTGAC[A/G]TGCTGAAGAATAATG | 26091 |
rs111484133 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HERC4 | GRCh38.p7 | 10:68014376 | GAATTCTGCATCACA[C/T]AGACAGGCTGCACGA | 26091 |
rs111500964 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:67990927 | ATATCTGCGGATGAT[C/T]AGGTTGTATAAGTTT | 26091 |
rs111508323 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67930692 | ATGGTATATTAGAAA[G/T]ATAGAAAATCAGCAG | 26091 |
rs111531963 | snp | A/C | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67945818 | AACTCAAATCAAAAA[A/C]CATACGACAGATACA | 26091 |
rs111544897 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HERC4 | GRCh38.p7 | 10:68020548 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 26091 |
rs111550670 | in-del | -/AT | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67939721 | CTATTTTACTTATGG[-/AT]ATATATATATATATA | 26091 |
rs111617068 | snp | C/G | 0.11298 | 0.209106 | intron-variant | HERC4 | GRCh38.p7 | 10:67925204 | TAAAAACAACATAAT[C/G]TTTTATTAGTATTAA | 26091 |
rs111641088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:67986993 | AAGGGGCAAAATACC[A/G]ACTATATAGGGTTTT | 26091 |
rs111673065 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68026434 | CTGCTATAATATACA[G/T]ATGTTTTTAAAAAAA | 26091 |
rs111700244 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68003368 | TTAGTAGAGATGGGG[G/T]TTCACTGTGTTAGCC | 26091 |
rs111743271 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67944782 | GAAGCAGAAATTCTA[A/G]AGTTGAAAAATGCAA | 26091 |
rs111829341 | snp | C/G | 0 | 0 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075820 | CTACTCTACTACCAC[C/G]ACCACCAGTTCAGTT | 26091 |
rs111833043 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68044710 | CTTAAACACACACTA[G/T]ATATAACCAGTTATT | 26091 |
rs111835794 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:67979312 | AATGAAGCAATAATT[C/T]TGGAGCTGAAAAAAT | 26091 |
rs111887479 | snp | C/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68062421 | CATTCTTTCTGCCTC[C/T]CTAAGTCTCCATCAT | 26091 |
rs111893984 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HERC4 | GRCh38.p7 | 10:67955759 | CTGGGCGACAAGAGC[A/G]AAACTCCGTCTCAAA | 26091 |
rs111951444 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | HERC4 | GRCh38.p7 | 10:68004104 | TCTGATGATGTTGAG[C/T]ACCTTTCATATACCT | 26091 |
rs112005998 | snp | C/T | 0.030665 | 0.119967 | intron-variant | HERC4 | GRCh38.p7 | 10:67987275 | ATGTTCAATTTCCCC[C/T]GCTTCTCTGCCCCTT | 26091 |
rs112040969 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68045066 | TGGCTCACGCCCATA[A/G]TACCAGCATTTTGGG | 26091 |
rs112115538 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HERC4 | GRCh38.p7 | 10:68015889 | AGGTGGATCACTTGA[A/G]GTCAGGAGTTCGAGA | 26091 |
rs112194675 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | HERC4 | GRCh38.p7 | 10:67942802 | AGGCGTGAGATACTG[C/T]GCCAGCTCCTGTTCC | 26091 |
rs112211450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:67983606 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 26091 |
rs112223359 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | HERC4 | GRCh38.p7 | 10:67946849 | GAGGTAGATGTTGCA[C/T]TGAGTCAAGATTGAG | 26091 |
rs112230911 | in-del | -/TAGT | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67930134 | CCTTTTAACACTTAG[-/TAGT]TATTCTGCTGAATAG | 26091 |
rs112273720 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | HERC4 | GRCh38.p7 | 10:68065895 | GTCTGTATAATTACA[C/T]ACAGCATAGGTTTTT | 26091 |
rs112274953 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:68027522 | GTTCACAAAATCAAT[A/C]CTAATTTCTTAATAT | 26091 |
rs112276482 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68076543 | CAACAGAAATTTATT[C/G]TCTCACAGTTCTGAA | 26091 |
rs112283989 | snp | C/T | | | intron-variant, missense | HERC4 | GRCh38.p7 | 10:68070567 | GCCGAGATGGCGCCA[C/T]TGCACTCCGGCCTGG | 26091 |
rs112375657 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68070259 | ACGAATTATTCCAAA[C/T]ATAAATAACTTTAGT | 26091 |
rs112467862 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:67989202 | ACATCCTTTAAATTG[C/T]ATTGCTCTAATACTA | 26091 |
rs112486297 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68072827 | TTATACGATGATTCA[A/G]ATTTAAAATGATATA | 26091 |
rs112528989 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67926732 | CTGGGAAAACCTCAG[G/T]GAACAGAATCCTCAC | 26091 |
rs112538407 | snp | A/C | 0.5 | 0 | synonymous-codon | HERC4 | GRCh38.p7 | 10:67936194 | TGCACCATTTAGAAC[A/C]AGCTCTTTCACTTCT | 26091 |
rs112619373 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HERC4 | GRCh38.p7 | 10:68007369 | CTGAACTTCCTCTGT[C/T]TATCTTCAGTTTAGT | 26091 |
rs112624013 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | HERC4 | GRCh38.p7 | 10:67972136 | GGAGAATCATTTGAA[C/T]CTGGGAGGCAGAGGT | 26091 |
rs112649843 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68046237 | AAAGATCTGTTATCT[C/T]AGAGGCTCCAGAAAA | 26091 |
rs112685280 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68013239 | ACACTTAGTAGACTA[C/T]AATATAGTATAAATA | 26091 |
rs112713740 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | HERC4 | GRCh38.p7 | 10:67966906 | GTCAACCAGGCTGGA[C/G]TGCAGTGGCACAATC | 26091 |
rs112719465 | in-del | -/T | 0.276534 | 0.248588 | intron-variant | HERC4 | GRCh38.p7 | 10:68057709 | AACTACACCTTATTA[-/T]TTTTTTTTTTCTTTT | 26091 |
rs112727367 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67938852 | AGGAGGCTGAGGCAG[G/T]AGAATCGCTTGAACC | 26091 |
rs112735342 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68019276 | GCTGAGATTACAGGC[A/G]TGAGCCACTGCGCCC | 26091 |
rs112748380 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67923337 | ATTTTTTCTTTAAAA[A/G]TATAATCTTAATACT | 26091 |
rs112808559 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HERC4 | GRCh38.p7 | 10:67970521 | TGCTTGAACCTAGGT[A/G]GTGGAGGTTGCAGTG | 26091 |
rs112889596 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HERC4 | GRCh38.p7 | 10:68008550 | TTGGGGATGTAATCA[C/T]ATGGATGTGGAAAAC | 26091 |
rs112919929 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68040174 | TGCCAAAAATTTTCT[A/G]AATTTGCATAGCAAT | 26091 |
rs112940550 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | HERC4 | GRCh38.p7 | 10:67930681 | TAAATCAGAGGATGG[C/T]ATATTAGAAAGATAG | 26091 |
rs112941056 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | HERC4 | GRCh38.p7 | 10:68058030 | AATCATTAAATAACC[G/T]TTTTAAAATCAATGA | 26091 |
rs112955290 | in-del | -/TAAA | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:67970175 | AGCTTAACTCCTGAC[-/TAAA]CTAAACTCAAATCCT | 26091 |
rs112967578 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HERC4 | GRCh38.p7 | 10:68030078 | AACAGTTTCTAGATT[C/T]CAAAGTCAAAAATTG | 26091 |
rs113003191 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HERC4 | GRCh38.p7 | 10:67979093 | GAGGAACATCTGTTA[A/G]GTTATCAAGACCATC | 26091 |
rs113072962 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:68062362 | ATACCTGGCTCTTTC[C/T]GTTACATTTACTATT | 26091 |
rs113098226 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HERC4 | GRCh38.p7 | 10:68049532 | GGAGGCAGAGGTTGC[A/T]GTGAGCCAAATTCAC | 26091 |
rs113121974 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67966979 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 26091 |
rs113129147 | snp | A/T | 0.444444 | 0.157135 | intron-variant | HERC4 | GRCh38.p7 | 10:67951959 | CCTCTCAGTTTCTGG[A/T]CCTGTCTGTTTCCAA | 26091 |
rs113134737 | snp | C/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67932889 | TCTGCTACATATCTA[C/T]GAAACTGAGAATGTA | 26091 |
rs113154246 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:67991051 | AAAAAAATAGAATAA[A/G]AATTTAAAATTATTT | 26091 |
rs113172029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68047982 | CAGGCTGAAGTGCAG[C/T]GGCATAATCATGGCT | 26091 |
rs113182485 | snp | A/G | | | intron-variant | HERC4 | GRCh38.p7 | 10:68068393 | TCGGGAGGCTGAGAC[A/G]GGAGAATCACTTGAA | 26091 |
rs113194334 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67987182 | ATCAAGTTCTTCCTT[A/G]GTTGAGACTGAAGTT | 26091 |
rs113261728 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67946997 | ATTACCGCTAAAGAG[A/G]GAGAGAGAGACCCCA | 26091 |
rs113298241 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67943093 | TTAGGAGTATTACTC[G/T]GTGTCATATTTGTTA | 26091 |
rs113307541 | snp | A/T | | | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68011628 | GTGGGCTTAAGCCCA[A/T]ATTAATATATTCAGT | 26091 |
rs113335054 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HERC4 | GRCh38.p7 | 10:67993373 | AAAGAAAGAATTGAA[C/T]TGGGCTACAGTGGCA | 26091 |
rs113390215 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68026626 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 26091 |
rs113399104 | snp | G/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67972386 | ATTAGCCGGGCATGG[G/T]GGTGCATGCCTGTAA | 26091 |
rs113408146 | snp | G/T | 0.144296 | 0.226554 | intron-variant | HERC4 | GRCh38.p7 | 10:67984842 | ACCGGCCTCAGCCTC[G/T]CAAAGTGCTGGGGTT | 26091 |
rs113413103 | snp | G/T | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67931174 | TTTAGTAGAGACGGG[G/T]TTTCACTATGTTGGT | 26091 |
rs113490463 | snp | A/G | 0.137867 | 0.223442 | intron-variant | HERC4 | GRCh38.p7 | 10:68020701 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAATGAGC | 26091 |
rs113492140 | snp | G/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68067912 | TTTTAGCTTTTGTTG[G/T]TACAATATTACATCT | 26091 |
rs113511299 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67993436 | AGGCAGGAGGATGGC[A/G]TGAGCCCAGTTCAAA | 26091 |
rs113530324 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67952844 | GGCAGAGCTTGCAGT[A/G]AGCCGAGAGTGCGCC | 26091 |
rs113532883 | snp | C/T | 0.138886 | 0.22395 | intron-variant | HERC4 | GRCh38.p7 | 10:67931088 | CTTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 26091 |
rs113569708 | snp | A/C/T | 1.68474e-05 | 0.00290231 | intron-variant | HERC4 | GRCh38.p7 | 10:67988881 | ATGAATTTTTTAAAA[A/C/T]ATCACAATTTTCAAA | 26091 |
rs113592732 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | HERC4 | GRCh38.p7 | 10:68027782 | ACAAAAATTAGCTGG[A/G]CGTAGTGGTGTGTGC | 26091 |
rs113631398 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:68013323 | TATTTGCTTTATTGC[A/G]CTATTTGCTTCATTG | 26091 |
rs113634272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67980197 | GCTCACCACAACCTT[C/T]GCCTTCCAGATAGTC | 26091 |
rs113733607 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68012022 | TTATGGAGATGGCTT[A/C]TTTCCTTAAACTTCA | 26091 |
rs113747738 | snp | C/T | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68012731 | CACAAAGTGAGCATA[C/T]ATGCTGTTGGAAAAA | 26091 |
rs113749183 | snp | A/T | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67975913 | CTATTACTAGCTTTC[A/T]AACAAAACAAAGACA | 26091 |
rs113769836 | in-del | -/C | 0.143284 | 0.226079 | intron-variant | HERC4 | GRCh38.p7 | 10:67929534 | ATAGTGCTTTTTTTT[-/C]TTTTTTGAGACAGGG | 26091 |
rs113787028 | snp | C/G | 0.164219 | 0.234823 | intron-variant | HERC4 | GRCh38.p7 | 10:67948814 | TAGTCCCAGCTACTT[C/G]GGAGGCTGAGGCACA | 26091 |
rs113797758 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HERC4 | GRCh38.p7 | 10:68064927 | GGGTGAGTGGAGATC[A/G]CGCCATGCACTCCAG | 26091 |
rs113816434 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67988644 | GGAAAGAGGAAAATA[A/G]AGGAATGATTGGACA | 26091 |
rs113840993 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | HERC4 | GRCh38.p7 | 10:68028606 | ATTGTGTCCAGATTA[C/T]ACATGGTTCATCACT | 26091 |
rs113845273 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68076423 | TTTATCTCTTGTTGA[A/C]AAACATGTTTTAGAT | 26091 |
rs113853240 | snp | A/G | 0.5 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:67977334 | ACCCACTGCCTCGAA[A/G]AGAAAGACCCAGTCC | 26091 |
rs113882981 | snp | C/T | | | missense | HERC4 | GRCh38.p7 | 10:67923017 | TATATTTTGGAAGAT[C/T]CAGAAGATTAAAACA | 26091 |
rs113888864 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:68067481 | AAATGTTCTGGTTCA[C/G]TAAGAAATGTGTGGG | 26091 |
rs113909661 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | HERC4 | GRCh38.p7 | 10:68046010 | TACTTACCTACTCCT[A/G]AAGCTTCCAGTACAT | 26091 |
rs113913773 | snp | A/G | 0 | 0 | intron-variant | HERC4 | GRCh38.p7 | 10:68055944 | TTTAGTAGAGGGGGG[A/G]TTTCACCATGTTGGA | 26091 |
rs113931032 | snp | G/T | 0.155987 | 0.23165 | intron-variant | HERC4 | GRCh38.p7 | 10:68051919 | AGCAACACGCCCGCC[G/T]CAGCCTCCCAAAGTG | 26091 |
rs114020877 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HERC4 | GRCh38.p7 | 10:68052230 | ATAACGACTTCGAAT[A/G]CATCTCTAATAGGTC | 26091 |
rs114028476 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | HERC4 | GRCh38.p7 | 10:68068892 | TCATCTGTAAAATGC[A/G]GACCATGATACCTGC | 26091 |
rs114032732 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HERC4 | GRCh38.p7 | 10:67961498 | AGAGAGTCAAAAAGA[C/T]CCTTGGCTGATTTTA | 26091 |
rs114036404 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HERC4 | GRCh38.p7 | 10:68004931 | CAAGATGAGATTTGG[A/G]TGGGGGCACAAAGCC | 26091 |
rs114039822 | snp | A/G | 0.067446 | 0.170804 | intron-variant | HERC4 | GRCh38.p7 | 10:67957812 | ATAGTCTGAATCTGC[A/G]TTTTTTTTTCCCCCA | 26091 |
rs114140216 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HERC4 | GRCh38.p7 | 10:68024804 | CTGCTCAATTTAATT[C/T]CCCCAAAGATGAAGC | 26091 |
rs114169097 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HERC4 | GRCh38.p7 | 10:67986902 | GGCATAAAATAAAAT[C/T]AAGCCCCCTTCTAAA | 26091 |
rs114268377 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | HERC4 | GRCh38.p7 | 10:68019292 | TGAGCCACTGCGCCC[A/G]GTCCAGCCAAAGCAT | 26091 |
rs114296443 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HERC4 | GRCh38.p7 | 10:67994535 | TCTCCCAAGTTCAAG[C/T]GATTGTCCCACCTCA | 26091 |
rs114346000 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HERC4 | GRCh38.p7 | 10:67969724 | ATATCAGTAGGACTA[A/G]AGGTCTGCAATTGCT | 26091 |
rs114364944 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:68064253 | CCAAAACATAAAAAA[G/T]AATTAAAAGAAAGAA | 26091 |
rs114411536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:68025808 | GTCTTCACAATTTAA[C/T]AGACAGATGGCTCTT | 26091 |
rs114436460 | snp | A/G | 0.15665 | 0.231917 | intron-variant | HERC4 | GRCh38.p7 | 10:67950727 | TCAGTTTGATTTCAC[A/G]GTCTTCAACATATAT | 26091 |
rs114481984 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | HERC4 | GRCh38.p7 | 10:68065292 | ATAATAGAAAACAAT[C/T]ATGAAAAACTAAAAA | 26091 |
rs114486768 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, nc-transcript-variant | HERC4, POU5F1P5 | GRCh38.p7 | 10:68010725 | GTTGAGCCTCAAAGA[A/G]GCAGATGGTCGTTTG | 26091 |
rs114488715 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HERC4 | GRCh38.p7 | 10:68049658 | CAGTGGCTCATGCCA[C/T]CTAGCACTTTGGGAG | 26091 |
rs114549705 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | HERC4 | GRCh38.p7 | 10:68053009 | GATGCTATATACTGA[C/T]AGTTTATTTCACTAC | 26091 |
rs114605118 | snp | A/G | 0.00377941 | 0.0433061 | intron-variant | HERC4 | GRCh38.p7 | 10:67957016 | AGTACAAGTTGATTT[A/G]TGATATACTTACTGT | 26091 |
rs114636243 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:68044135 | TATAACCCACTAAAA[A/T]AATTTGTAATGAAGC | 26091 |
rs114661831 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:68005174 | TTTATTGGGGTCTGT[C/T]TCTTGTTAGCTCTAA | 26091 |
rs114746343 | snp | A/T | 0.0663309 | 0.169604 | intron-variant | HERC4 | GRCh38.p7 | 10:67960391 | TATTAAAAGCCTAAA[A/T]TTTTTTTTTTTGAGA | 26091 |
rs114787676 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:67984382 | CATTATTTAAGTGAA[A/C]TAAGCCAGGCACAGA | 26091 |
rs114788596 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HERC4 | GRCh38.p7 | 10:68064319 | AGCAATTTGGGATGT[C/T]GTGGCAGATGGATCA | 26091 |
rs114840591 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HERC4 | GRCh38.p7 | 10:68059259 | TCATTGAGATCATAC[C/T]AAATTTACAAATTAG | 26091 |
rs114844284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67954288 | TAAATTAATTTTTCC[C/T]AACAGAAAAGTTAAT | 26091 |
rs114875049 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | HERC4 | GRCh38.p7 | 10:67975714 | TGTGGCTTAGCATTG[C/T]ACAAATAATCCAATT | 26091 |
rs114927373 | snp | C/T | 0.153332 | 0.230554 | intron-variant | HERC4 | GRCh38.p7 | 10:67978778 | GTGCCTCAGAACAGA[C/T]AAAGTTTGTTTTGGA | 26091 |
rs114960309 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HERC4 | GRCh38.p7 | 10:68008961 | CGCAGTGGTTCACTC[C/T]TGTAATCCCAGCACT | 26091 |
rs114991782 | snp | C/T | 0.067446 | 0.170804 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68011912 | GCTGTTTTGTCAACA[C/T]TGAAAATCTGTTGTT | 26091 |
rs114997655 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:67969620 | CACTGAGGAAGGGGA[C/T]GCAAACCCATGTCTT | 26091 |
rs114999643 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC4 | GRCh38.p7 | 10:67936640 | TCCAGGGTTCCTCTA[C/T]CACCCTTGTTGTAAA | 26091 |
rs115008500 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | HERC4 | GRCh38.p7 | 10:67961321 | TTTTGGTTCCTTGAG[A/T]CCTGGTGACTAGTGT | 26091 |
rs115033260 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | HERC4 | GRCh38.p7 | 10:67962833 | CAGAGTTATTAGACA[C/T]GTCAGAATAAAAGCT | 26091 |
rs115143453 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HERC4 | GRCh38.p7 | 10:67990798 | ATTTTAAAAGCACAT[C/T]GTAAGAGTCTGTGAA | 26091 |
rs115252060 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | HERC4 | GRCh38.p7 | 10:68034515 | CTCATTTTTATTTTA[C/T]AGTTTCTCCCAAGAG | 26091 |
rs115256237 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069699 | ACCTATGTAAAGAAA[C/T]AATTCTTAGTTCCCT | 26091 |
rs115326192 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:67935753 | TGGGAAACTAGTTTC[C/T]AACTGCTTCTTATAA | 26091 |
rs115463976 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:67984403 | CAGGCACAGAGACAA[A/C]TATCGCATGTTCTCA | 26091 |
rs115467556 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HERC4 | GRCh38.p7 | 10:67967395 | GATTAAACTGTATAC[A/G]GTATATATAAACTAG | 26091 |
rs115500834 | snp | C/T | 0.000780193 | 0.0197354 | intron-variant | HERC4 | GRCh38.p7 | 10:67932565 | ATATAAATCTTTCCA[C/T]TTAACAATATCAGAG | 26091 |
rs115514036 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC4 | GRCh38.p7 | 10:67953577 | AAGATGGGACAATAT[A/G]AGCATCAATGAAGAC | 26091 |
rs115605403 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, downstream-variant-500B | HERC4 | GRCh38.p7 | 10:67966302 | TAGTCTTGAAGCACC[A/G]ATTTCACAACAATAA | 26091 |
rs115705343 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HERC4 | GRCh38.p7 | 10:67976845 | TCCTGTCCACAGAGG[A/G]AGCATTAAAACCCAG | 26091 |
rs115707115 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | HERC4 | GRCh38.p7 | 10:67947386 | AATATTGATAACAGG[A/G/T]TCAATTCATCAAGAA | 26091 |
rs115714744 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | HERC4 | GRCh38.p7 | 10:68023163 | AAAAACAGAATTGCC[A/G]TATGAACCACCAATT | 26091 |
rs115875585 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HERC4 | GRCh38.p7 | 10:68052605 | CAAAATATTACATAA[C/G]AAAGTACTTCCTGTT | 26091 |
rs115893043 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | HERC4 | GRCh38.p7 | 10:68015618 | GGTTTTGATTCAAGA[C/G]TTTTCAAGTTAGCTA | 26091 |
rs115998381 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:67943894 | TAGAGTGGGAACAAT[G/T]TTGCCTTGTGGCTTG | 26091 |
rs116003419 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | HERC4 | GRCh38.p7 | 10:67959618 | AAAAATAAGCCATAA[A/G]TTGTTTTTATTTGAC | 26091 |
rs116110607 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HERC4 | GRCh38.p7 | 10:68065832 | ACCACTGTACTCCAG[C/T]GACAACAAGATCCTG | 26091 |
rs116175362 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68077069 | GACGGAGGTTTTGCG[A/G]TGAGCCTAGAGCGCG | 26091 |
rs116322672 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | HERC4 | GRCh38.p7 | 10:68003868 | TCCTTTCTTTTGGGT[A/G]TATACCCAGCAATGG | 26091 |
rs116351124 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HERC4 | GRCh38.p7 | 10:68023128 | CTATGAGAAACAGTA[C/T]GGCAGTTCCTACAAA | 26091 |
rs116374612 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | HERC4 | GRCh38.p7 | 10:67975898 | ACCAGAGTTATACTG[C/T]TATTACTAGCTTTCA | 26091 |
rs116493332 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HERC4 | GRCh38.p7 | 10:67943866 | CACCTAATTATTCTA[C/T]GGATGGGGCCTGTAG | 26091 |
rs116494574 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HERC4 | GRCh38.p7 | 10:68017184 | TGTGTATTTGTCTCC[A/G]TCAGAAGAATACCCA | 26091 |
rs116521733 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HERC4 | GRCh38.p7 | 10:68026152 | CCAGGCTTGAGTGCC[A/G]TGGCATGATCATGGC | 26091 |
rs116523038 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:68035812 | GTTCATTTCAACTCT[A/C]TCCCAGCAGGAGCCT | 26091 |
rs116548874 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HERC4 | GRCh38.p7 | 10:68054052 | CTGTCCTACCATGCC[C/T]CATTAGTTGTTAAAA | 26091 |
rs116572004 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:67951669 | CCTTCATATGATTGC[A/G]TCTAGAGCTAAGGTA | 26091 |
rs116604402 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HERC4 | GRCh38.p7 | 10:68039025 | GGGGGATGCCAGATG[C/T]GGATTACAGGTGGGT | 26091 |
rs116634232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069535 | AACACCTCTTTTCAA[C/T]AGGCCACAGGTTAAA | 26091 |
rs116715134 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | HERC4 | GRCh38.p7 | 10:68063166 | TCATTAAATGATATT[C/G]ATCATGTTGTAATAG | 26091 |
rs116720505 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | HERC4 | GRCh38.p7 | 10:67927156 | GCATGGAATTTATGG[A/C]ATTTATTCAACTGTT | 26091 |
rs116745972 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HERC4 | GRCh38.p7 | 10:67949755 | CACATAGCTGGGCGC[A/G]GTGGCTCACGCCAGC | 26091 |
rs116803299 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | HERC4 | GRCh38.p7 | 10:68008780 | AGAAACAACCCAATC[A/G]TCCACTGATATATGA | 26091 |
rs116829553 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | HERC4 | GRCh38.p7 | 10:67960336 | TGTGTTTCTTCCCTT[C/G]GCTGATTTTTGTTCT | 26091 |
rs116839465 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HERC4 | GRCh38.p7 | 10:67953782 | TAAGGAATCAGAAAA[C/T]GTGAGGAAATTTCTC | 26091 |
rs116881803 | snp | G/T | 0.155325 | 0.23138 | intron-variant | HERC4 | GRCh38.p7 | 10:67978562 | TGCCCCGAAGGGAAG[G/T]ACACAGGCCAGGCTG | 26091 |
rs116900394 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:67924142 | TCCATGGATTGAACC[A/G]ACTGCAAATCGAAAA | 26091 |
rs116937276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67947706 | CCATATGTTAGGTCA[C/T]AAAACTTTCAATAAA | 26091 |
rs116991245 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HERC4 | GRCh38.p7 | 10:68045349 | AAAAAGGAAATTAAG[A/G]AAATAATCTGAATTA | 26091 |
rs116998622 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68075590 | AGCCTTTTAATGAAG[A/C]AAATCACTTTGTTTT | 26091 |
rs117012037 | snp | A/G | 0.152667 | 0.230274 | intron-variant | HERC4 | GRCh38.p7 | 10:68029437 | GTGGACGTTACAGTG[A/G]GCCGAGATCGCACCA | 26091 |
rs117017721 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HERC4 | GRCh38.p7 | 10:68051006 | CTATCACCAAAGTAC[A/G]TTTACCTTTAAAGGC | 26091 |
rs117022651 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | HERC4 | GRCh38.p7 | 10:67959921 | ACTAAATTTGTGGAC[A/G]GTGCCTTGTGTTGTG | 26091 |
rs117027771 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HERC4 | GRCh38.p7 | 10:68023540 | AGAATGGTGGTTGCC[A/C]CAAGAGAGTATGGAG | 26091 |
rs117045979 | snp | C/T | 0.157972 | 0.232445 | intron-variant | HERC4 | GRCh38.p7 | 10:67929345 | CTTAGATGCCTCTTG[C/T]GCTACCTCCTCTGAA | 26091 |
rs117063052 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HERC4 | GRCh38.p7 | 10:68051963 | CATGAGCCACCGCGC[C/T]CAGCCTCAACTTTTC | 26091 |
rs117089739 | snp | A/T | 0.153332 | 0.230554 | intron-variant | HERC4 | GRCh38.p7 | 10:68034724 | ATCCTACTTCCCTGG[A/T]CCTCTTTCCAGTGCT | 26091 |
rs117089882 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HERC4 | GRCh38.p7 | 10:67957684 | TTCTACCATCTACCC[A/G]GTAAAACAATATCTT | 26091 |
rs117107570 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68074998 | GGGGCGGCCCCTGCC[C/G]AGAGAGCAAGGCAGC | 26091 |
rs117129912 | snp | A/C | 0.0825414 | 0.185628 | intron-variant | HERC4 | GRCh38.p7 | 10:67995708 | TTTTCCATTTAAACA[A/C]ATTTATCTAATTCTT | 26091 |
rs117131627 | snp | A/C | 0.154661 | 0.231107 | intron-variant | HERC4 | GRCh38.p7 | 10:68046967 | TGTCTCCAGAAAAAC[A/C]AACAAACAAACAAAC | 26091 |
rs117149734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HERC4, POU5F1P5 | GRCh38.p7 | 10:68010642 | GAATATTTTCATTGT[A/T]GTCGGCTTCCTCCAC | 26091 |
rs117166082 | snp | C/T | 0.15665 | 0.231917 | intron-variant | HERC4 | GRCh38.p7 | 10:68006233 | TCTGTGTACTTACTA[C/T]TATCGTGAGTTTTGT | 26091 |
rs117189362 | snp | A/G | 0.158044 | 0.233655 | intron-variant | HERC4 | GRCh38.p7 | 10:68031895 | AGTAGCTGGGGATAG[A/G]TGCCTGCCGCCATGC | 26091 |
rs117191521 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:67922810 | TGAACACTCGTAGAT[C/T]GAACATTCTGCAAGT | 26091 |
rs117214564 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HERC4 | GRCh38.p7 | 10:68016198 | CTCTAGATTTGATGT[A/G]AGAGCTCGAAAGCAC | 26091 |
rs117250878 | snp | A/G | 0.154661 | 0.231107 | intron-variant | HERC4 | GRCh38.p7 | 10:68048463 | GCTGGAAAAGACAAC[A/G]ATGGAGACAGTAAAA | 26091 |
rs117300485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68049936 | ACAAGGCCAGACGCA[A/G]TGGCTTATGCCTGTA | 26091 |
rs117303447 | snp | A/G | 0.154329 | 0.23097 | intron-variant | HERC4 | GRCh38.p7 | 10:68003725 | ATAGTATTCCATTGT[A/G]TATATATACACCACA | 26091 |
rs117311764 | snp | A/G | 0.155325 | 0.23138 | intron-variant | HERC4 | GRCh38.p7 | 10:68004848 | AGCATGCAGGAAACC[A/G]ATTCCATGATTCCAT | 26091 |
rs117330564 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | HERC4 | GRCh38.p7 | 10:68004312 | TAATTCCTTATCAGA[C/T]GGGTAGTTTGCAAAT | 26091 |
rs117339813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67924460 | AACCTGTACAGCATG[C/T]TACTGTACTGAATTC | 26091 |
rs117353109 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HERC4 | GRCh38.p7 | 10:68050361 | CAAACAATAAATAAA[A/G]TATAACTTAAAAAAT | 26091 |
rs117372673 | snp | C/T | 0.156319 | 0.231784 | intron-variant | HERC4 | GRCh38.p7 | 10:67950012 | GGATAGAGCAAGACT[C/T]CATCAATCAAAAAAA | 26091 |
rs117386117 | snp | A/G | 0.157972 | 0.232445 | intron-variant | HERC4 | GRCh38.p7 | 10:67929566 | CTTGCTTTGCTGCCT[A/G]TGACAGAGTGCAGTC | 26091 |
rs117393829 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HERC4 | GRCh38.p7 | 10:67953355 | TTAGGGTATACTCTT[C/T]GTACAAAAAGAACTG | 26091 |
rs117421337 | snp | A/G | 0.153332 | 0.230554 | intron-variant | HERC4 | GRCh38.p7 | 10:68018525 | CAATTATATAAACAC[A/G]TTAAGTATAAATAAT | 26091 |
rs117468510 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HERC4 | GRCh38.p7 | 10:68034982 | TTTGCTCCCATATTG[C/T]CATCGTATTTTGCAA | 26091 |
rs117469140 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HERC4 | GRCh38.p7 | 10:67927952 | GCAAAATAAAACAGC[A/G]AGGGGAGACAGGATA | 26091 |
rs117474058 | snp | G/T | 0.0333695 | 0.124785 | upstream-variant-2KB | HERC4 | GRCh38.p7 | 10:68076328 | GCTGGTCTCAAACTC[G/T]TTACCTCAGGCGATC | 26091 |
rs117478658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67982218 | GACTTCAAATTATAG[C/T]GCAGCGGTATAGTAA | 26091 |
rs117496261 | snp | A/C | 0.157972 | 0.232445 | intron-variant | HERC4 | GRCh38.p7 | 10:67983086 | TGAGCAAAAAAAAAA[A/C]AAAACAAAACAAAAA | 26091 |
rs117515875 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | HERC4 | GRCh38.p7 | 10:67935106 | TTTTGACTGTTTTGG[C/T]CTTTCCTTAAATGTC | 26091 |
rs117544194 | snp | A/C | 0.152334 | 0.230133 | intron-variant | HERC4 | GRCh38.p7 | 10:68028151 | TTATGAGCTGGAATT[A/C]TTCTATAAATAACTT | 26091 |
rs117548219 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HERC4 | GRCh38.p7 | 10:67964656 | TATCATTAACACTTT[A/G]GATAAAATCCAAATT | 26091 |
rs117594746 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HERC4 | GRCh38.p7 | 10:68049162 | AAGATTCCATCTACA[C/T]GCTGAAATATTATGC | 26091 |
rs117616775 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | HERC4, POU5F1P5 | GRCh38.p7 | 10:68011119 | CCAGGCTGGAGTGCA[C/T]TAGTATGATCATAGC | 26091 |
rs117633110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67977616 | GACTTGGTTCTTAGA[C/T]GGCATTTCTGGACCT | 26091 |
rs117639735 | snp | A/G | 0.15698 | 0.23205 | intron-variant | HERC4 | GRCh38.p7 | 10:67995386 | CTTATAACAGGAAAG[A/G]GAGGATTAATGCTTG | 26091 |
rs117670172 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HERC4 | GRCh38.p7 | 10:68023430 | CCTTGATGACACTAC[A/G]CTGAGTGAGATAAGT | 26091 |
rs117723121 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HERC4 | GRCh38.p7 | 10:68009292 | TGGTTTTTCTTTTTT[A/T]TCTTTTATAGAGATG | 26091 |
rs117723916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:68071297 | ATACAGTTGGAGGCT[C/G]TTCCTGGCACTATAA | 26091 |
rs117726316 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | HERC4 | GRCh38.p7 | 10:67939101 | AATAAGACAAGATGG[G/T]CAAGGATGAATGTTA | 26091 |
rs117766886 | snp | G/T | 0.153997 | 0.230832 | intron-variant | HERC4 | GRCh38.p7 | 10:67987746 | CCAGAAAGTTAAGTA[G/T]TTGAGAAAAATACCC | 26091 |
rs117775182 | snp | A/T | 0.152667 | 0.230274 | intron-variant | HERC4 | GRCh38.p7 | 10:68031768 | AATGCCTCTTTTTTT[A/T]TGAAACGAGGTCTCA | 26091 |
rs117804058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67973330 | ACATGGAGCAAAACT[A/G]GATTCAACATGCAGT | 26091 |
rs117811241 | snp | A/T | 0.0158469 | 0.0875917 | utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:67921913 | CTGAAAGTTTAAATA[A/T]TAAAACAATAAATCT | 26091 |
rs117835009 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HERC4 | GRCh38.p7 | 10:68048304 | AGGTGAATGGATAAA[C/T]TGTGGTACATCCAGA | 26091 |
rs117842527 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HERC4 | GRCh38.p7 | 10:68072409 | AAATCAAATAAAATT[A/G]CATATTTAAAATACT | 26091 |
rs117880827 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | HERC4 | GRCh38.p7 | 10:67956326 | TAAATGAAAGAACTC[C/T]CAACATAAAATGGAT | 26091 |
rs117911144 | snp | A/G | 0.137867 | 0.223442 | intron-variant | HERC4 | GRCh38.p7 | 10:67927717 | GGCATGAGCCACTGC[A/G]CCCGGCCGCTACAAT | 26091 |
rs117916879 | snp | C/G | 0.15698 | 0.23205 | intron-variant | HERC4 | GRCh38.p7 | 10:67972927 | AGTTAACTTCCTTAA[C/G]AGAAATAATGCTACT | 26091 |
rs117943484 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | HERC4 | GRCh38.p7 | 10:68005901 | AATGGGGTATCACTA[G/T]GTTGCCTAGGCTGAT | 26091 |
rs117943992 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HERC4 | GRCh38.p7 | 10:67932248 | AGGTGTAAGCCACCA[C/T]GCCTGGCCTAAGTTA | 26091 |
rs117949557 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | HERC4 | GRCh38.p7 | 10:67960119 | TGCTTCCAGAAGAGC[C/T]GGGAACTAGAGGTCA | 26091 |
rs117954522 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HERC4 | GRCh38.p7 | 10:68067552 | TAACTTTATTTCCCA[C/T]AGTTATATTTTCCTA | 26091 |
rs117995650 | snp | C/G | 0.153997 | 0.230832 | intron-variant | HERC4 | GRCh38.p7 | 10:67987706 | GGAATCTTGGACATA[C/G]TAAATACCAAAGAAA | 26091 |
rs118007110 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HERC4 | GRCh38.p7 | 10:68051022 | TTTACCTTTAAAGGC[C/T]AATAACACAATTAGA | 26091 |
rs118008277 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | HERC4 | GRCh38.p7 | 10:67960224 | AAATACTCTGTATTG[G/T]TACACATCTATGCCA | 26091 |
rs118049198 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC4 | GRCh38.p7 | 10:67971127 | AAATGTCTATATTTA[C/T]TTTTTAAATTTAATA | 26091 |
rs118079156 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | HERC4 | GRCh38.p7 | 10:67924738 | CAGGGAGGTCTTGGA[A/C]TCAATCCCCCATGTA | 26091 |
rs118130792 | snp | C/G | 0.154993 | 0.231244 | intron-variant | HERC4 | GRCh38.p7 | 10:67979599 | AAGTAGAAGACTGTA[C/G]AACACCAAGCAGACT | 26091 |
rs118153679 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HERC4 | GRCh38.p7 | 10:68006161 | TGCTGTAGTTATTAT[C/T]ATCTTTGATCCGTTT | 26091 |
rs118158705 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HERC4 | GRCh38.p7 | 10:67928084 | ATTATCAGGGGAAGA[A/G]AATTCCAGGCACTTG | 26091 |
rs118184264 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HERC4 | GRCh38.p7 | 10:68043555 | GCACAGTGCTTCACG[C/T]CTATAATCATGAGTA | 26091 |
rs137855098 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HERC4 | GRCh38.p7 | 10:67989010 | TATAAACCTCCCCCC[A/G]ACCAAGTTAAACAAT | 26091 |
rs137859444 | snp | C/T | 3.40715e-05 | 0.0041273 | intron-variant | HERC4 | GRCh38.p7 | 10:67932822 | AGATTATAAAAATCA[C/T]GTATGAAGAATCCAT | 26091 |
rs137864053 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:68025065 | TGTTGCTACTAAAAA[C/T]TAAAAAAATAAAATT | 26091 |
rs137975620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HERC4 | GRCh38.p7 | 10:67995559 | TGTCTTATTTATCTA[C/T]TAGCTGTCTTTTTTT | 26091 |
rs137998842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | HERC4 | GRCh38.p7 | 10:68069770 | GAAGTCAGCTGGGCA[C/T]GGTGGCTCACGCCTG | 26091 |
rs138006662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HERC4 | GRCh38.p7 | 10:67976569 | TTAACAACTATCTAC[A/C]CAAAAAAAGCATCTT | 26091 |
rs138028356 | snp | A/T | 0.0119087 | 0.0762398 | synonymous-codon, intron-variant, nc-transcript-variant | HERC4 | GRCh38.p7 | 10:68032856 | TGACTTTAGTAAATT[A/T]GGAACATACCTATCT | 26091 |
rs138032440 | snp | C/T | | | intron-variant | HERC4 | GRCh38.p7 | 10:67983611 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 26091 |
rs138040388 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HERC4 | GRCh38.p7 | 10:67990687 | ACAAACTTAAGCAAC[A/G]TGGTAATGTTAAGTA | 26091 |
rs138043413 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HERC4 | GRCh38.p7 | 10:68049894 | CAAGCCTGGGAGATA[A/G]TAAGACGGTCTCAAA | 26091 |
rs138050970 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | HERC4 | GRCh38.p7 | 10:67938127 | CAGGGTGGCAAACAA[A/G]TATACAAGCAAAAAA | 26091 |
rs138113358 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | HERC4 | GRCh38.p7 | 10:67949049 | ACAAGGTCAGGAAAT[A/C]GAGATCATCCTGGCT | 26091 |
rs138161485 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HERC4 | GRCh38.p7 | 10:67944785 | GCAGAAATTCTAGAG[C/T]TGAAAAATGCAACTG | 26091 |