SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs768197 | snp | G/T | 0.460477 | 0.134905 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923930 | GAAACATGGCCCTCT[G/T]CTCAGGTCCTGTGGC | 25909 |
rs903462 | snp | C/G | 0.49621 | 0.0433651 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932608 | TAGAAAAAACAGCAC[C/G]GTGGAAAAAGCGTTT | 25909 |
rs903464 | snp | C/T | 0.097727 | 0.198275 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907921 | TGTTAAACTAGAAAA[C/T]TGCCATCCTTATCTA | 25909 |
rs903465 | snp | A/G | 0.093417 | 0.194889 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908051 | TAACAACCATAAATA[A/G]AACTGATTTATTTCT | 25909 |
rs923972 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916871 | CTAAGGCTTAAACGA[C/T]TTAAACTAGAAGTTA | 25909 |
rs967953 | snp | A/C/G/T | 0.0934559 | 0.195063 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894866 | TCCCAAGTTGCCTCC[A/C/G/T]TGAAGTGTTGATGTT | 25909 |
rs1039009 | snp | A/C | 0.461259 | 0.133677 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917156 | GAAGCACAGAGTAGC[A/C]GCACTGGGTGGAAGA | 25909 |
rs1039010 | snp | A/G | 0.434976 | 0.168179 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918081 | AGGTTCACTGATAAC[A/G]TGTTTAAGAGCTTAT | 25909 |
rs1047080 | snp | A/G | 0.233818 | 0.249476 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840729 | AAATATCTAGTTTGG[A/G]AGAAAATAATTTATA | 25909 |
rs1047085 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840721 | AGTTTGGAAGaaaat[A/C]atttatataaattat | 25909 |
rs1053916 | snp | A/G | 0.0205511 | 0.0992634 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839173 | CTAAATGAACTTTAC[A/G]TATATTTTAAATGAA | 25909 |
rs1472275 | snp | A/G | 0.483053 | 0.0904792 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891228 | GACCAAAGTAAACTA[A/G]ATACAAAGATGAATT | 25909 |
rs1472276 | snp | C/G | 0.0782148 | 0.181884 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867173 | Gtaatttttaattat[C/G]tttaacattttatag | 25909 |
rs1472277 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866950 | TGTTAGTAGACCTCT[A/G]AATGAGGGTTGTTTT | 25909 |
rs1612610 | snp | G/T | 0.460252 | 0.135255 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905224 | TATGTATCAGGCCAG[G/T]CGTGGTGACTCACAC | 25909 |
rs1613209 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871877 | CTGTGTCTTTAGGTT[A/G]TTATTATTTTTTAAT | 25909 |
rs1616541 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871547 | GTATACCTTGTTTTT[C/T]TGGGCCCCTTTCTGT | 25909 |
rs1619941 | snp | A/T | 0.454784 | 0.1434 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929478 | GACCTGAAATTTGAG[A/T]ATTTAAAAAAGGAAA | 25909 |
rs1630829 | snp | C/T | 0.435694 | 0.167385 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860564 | AACTCTCATGCTTTC[C/T]TTCTGAGATAGGGTC | 25909 |
rs1691238 | snp | A/G | 0.108755 | 0.206276 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928140 | CCCCATCTCTACTAA[A/G]AATACAAAAAAAATT | 25909 |
rs1691239 | snp | G/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880178 | ATTTACATGCTTCAG[G/T]GTTTAAGAGCTAAGA | 25909 |
rs1691240 | snp | A/C | 0.460252 | 0.135255 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904579 | GTATGGGAAGGAGAA[A/C]GGGCAGTTGGGGGAA | 25909 |
rs1691241 | snp | A/G | 0.460365 | 0.13508 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904829 | TTTACTTGGCTTCTA[A/G]CACACCACACCTTCC | 25909 |
rs1691242 | snp | A/G | 0.46014 | 0.13543 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905365 | TAGCCAGGCATGGTG[A/G]CAGGCACCTGTAGTC | 25909 |
rs1691243 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906212 | TTGACCAAGAGATGA[C/T]AGTGTTAGAGAAAGC | 25909 |
rs1691251 | snp | A/G | 0.431177 | 0.172264 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864477 | TGAATTTTAGTAAAT[A/G]GATTGCCAGGGAAGC | 25909 |
rs1691252 | snp | C/T | 0.433818 | 0.169443 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900847 | acctaaaacggatgc[C/T]tttgggcattaaggc | 25909 |
rs1691253 | snp | C/T | 0.108048 | 0.20579 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901686 | AGCCAGGTGTGGTGG[C/T]GTGTGCCGGCAGTCC | 25909 |
rs1691254 | snp | A/G | 0.46014 | 0.13543 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901773 | caaccagccaagatc[A/G]tgccaccacactctg | 25909 |
rs1691255 | snp | A/G | 0.485933 | 0.0826777 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902170 | GCGATGACACTAAAG[A/G]AGACAGAGAAAACAT | 25909 |
rs1691256 | snp | G/T | 0.0970103 | 0.197722 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902296 | GCCTGTTTTGAGAAC[G/T]AGATTAAAATAAAAG | 25909 |
rs1691257 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903806 | ttgcaccactgcact[A/C]cagcctgggcgacag | 25909 |
rs1779964 | snp | A/G | 0.476918 | 0.104919 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899907 | ACATATAAATACTAA[A/G]TTTCTTGTGTGTATA | 25909 |
rs1779965 | snp | G/T | 0.0973687 | 0.197999 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901978 | TGGGTAAGTTCGCTG[G/T]GTGATTTAATCCTCA | 25909 |
rs1779966 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903831 | cgacagagcgagact[C/T]tgtctcaaaaaaaaa | 25909 |
rs1779967 | snp | A/T | 0.465052 | 0.127485 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904790 | GATCCCTTTTAATAA[A/T]TCCTATTACTAGTTC | 25909 |
rs1779968 | snp | A/T | 0.453087 | 0.145793 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906395 | CCAGTCTGACCAACA[A/T]GGTGAAAATCCGTCT | 25909 |
rs1779969 | snp | C/T | 0.485731 | 0.0832509 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906647 | TTGAGATACACTTCC[C/T]ATAAGATAAATTACT | 25909 |
rs1779971 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880211 | taaCAAATAACATAT[G/T]GTTTTGGATAATAAG | 25909 |
rs1779972 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880205 | ATAACATATGGTTTT[G/T]GATAATAAGCTATTT | 25909 |
rs1779973 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882638 | AACCCACCTAACAAA[C/G]AGGAAAAATTATGCC | 25909 |
rs1779975 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908936 | CTTAATGAATGAAAC[A/C]ATTAGCTCAAAGTAA | 25909 |
rs1779976 | snp | A/C/G | 0.00404816 | 0.0448079 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888139 | AATTTTATAATTTTA[A/C/G]TAATACATGAAACAC | 25909 |
rs1779977 | snp | A/G | 0.495174 | 0.0488838 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869776 | cctgtacatcatcag[A/G]gctcctgggtgacca | 25909 |
rs1779978 | snp | A/T | 0.467132 | 0.12391 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869579 | ttaagggccttagga[A/T]ttttggaatggtgat | 25909 |
rs1779979 | snp | A/G | 0.499713 | 0.0119774 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869138 | ACAAAACACACGGCC[A/G]GGCGTGGTGGCTCAC | 25909 |
rs1779980 | snp | C/T | 0.429837 | 0.173662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869133 | ACACACGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 25909 |
rs1779981 | snp | A/G | 0.11963 | 0.213316 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869001 | aaaagttagccaggc[A/G]tggtggcgggcgcct | 25909 |
rs1779982 | snp | A/G | 0.48666 | 0.0805725 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868937 | GAATGGCGTGAACCC[A/G]GGAGGCAGAACTTGC | 25909 |
rs1812703 | snp | A/G | 0.108048 | 0.20579 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925347 | AAAAGCATTTTTTGG[A/G]AAATGAAATATAGTA | 25909 |
rs1892116 | snp | C/T | 0.375598 | 0.21616 | | | GRCh38.p7 | 1:246917020 | GTCATGTTTGGATTT[C/T]ACCCTGCCTGCAATG | 25909 |
rs2011875 | snp | A/G | 0.093777 | 0.195178 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908130 | CTGATTCCGGGTCAG[A/G]GGGAAGAAAATACAT | 25909 |
rs2029789 | snp | A/T | 0.375 | 0.216506 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930586 | CCCTTTTTTTTTTTT[A/T]AACTGTTTTTTTGTG | 25909 |
rs2047190 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926469 | GTTTAATAAAGTTTT[C/T]CAAATTTAACAGCCT | 25909 |
rs2047191 | snp | A/G | 0.386884 | 0.209196 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926788 | ttgaacccgggaggc[A/G]gagattgcagtcagc | 25909 |
rs2047192 | snp | A/G | 0.388964 | 0.20782 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926904 | TATggccgggccgcg[A/G]tggcacacgcctgta | 25909 |
rs2067915 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876670 | GCAGTAGGAGTTACA[C/T]AGTACAAAGATCATT | 25909 |
rs2067916 | snp | A/G | 0.329084 | 0.237162 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876646 | GATCATTGTGTGGTA[A/G]AGGAAGACGTAGAGG | 25909 |
rs2172796 | snp | A/G | 0.460702 | 0.134554 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924316 | GCATTTCATACAATA[A/G]TCTCTATGAATTCTT | 25909 |
rs2379094 | snp | A/C | 0.0652144 | 0.168387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866902 | TAATCTTGGGTAGCT[A/C]ATTGAAGCTTTCTTC | 25909 |
rs2379188 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908322 | TTTTTTTTTTTTTTG[G/T]ATCCCTGTGAATTTT | 25909 |
rs2493606 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923325 | gaggctgaggcatga[A/G]aactgcttgaaccta | 25909 |
rs2642975 | snp | A/T | 0.4628 | 0.13121 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928884 | TTTCAGAAATTTCTT[A/T]CCAACTTAATTCAAA | 25909 |
rs2642976 | snp | C/T | 0.448836 | 0.15154 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929012 | CTAGAAAAGGAGATA[C/T]ATAGTCAATTATCAG | 25909 |
rs2642977 | snp | C/T | 0.462144 | 0.132269 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929076 | TAGAGGTACATATGC[C/T]GTGAGATCCCAGTAA | 25909 |
rs2642984 | snp | G/T | 0.474453 | 0.110094 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881390 | GTGTCCTGAATAATT[G/T]TTTTTCCTAGTCTGT | 25909 |
rs2642985 | snp | A/T | 0.0941369 | 0.195465 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880645 | TCATAAATTAAGTTT[A/T]TCTTACTCCTGCTAG | 25909 |
rs2642986 | snp | C/T | 0.116488 | 0.211364 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874984 | GTTTCTTCCTAAACC[C/T]CATGTAAAATATTAG | 25909 |
rs2642990 | snp | C/T | 0.491245 | 0.0655821 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885532 | TGAAGGATAACATCG[C/T]TACCACTGGACACTG | 25909 |
rs2642991 | snp | A/G | 0.46014 | 0.13543 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886437 | tacattgtattagat[A/G]ttataagtaatctac | 25909 |
rs2800214 | snp | C/T | 0.461481 | 0.133325 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914396 | CATGTGTTAAAAAGA[C/T]TAAAAGTTGTTTCAG | 25909 |
rs2800215 | snp | A/G | 0.462472 | 0.13174 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928595 | CTGGTTCAGTATTAA[A/G]CAAAACAAAATTCTT | 25909 |
rs2800219 | snp | A/C | 0.460589 | 0.13473 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892125 | AAGCCAAGAGTGAGA[A/C]TATGAACTCAAATCA | 25909 |
rs2800220 | snp | C/T | 0.473909 | 0.111197 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894512 | CGCGCCACTGCACTA[C/T]AGCCTGGCGACAGAG | 25909 |
rs2800221 | snp | C/T | 0.460925 | 0.134204 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895403 | TGAACAGACAATATG[C/T]GTTTGGGGTGTGTGT | 25909 |
rs2800222 | snp | C/G | 0.434906 | 0.16979 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867935 | TAAAATTTTTAGCTA[C/G]TATTACCACGTAATG | 25909 |
rs2818888 | snp | C/T | 0.461037 | 0.134028 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925561 | ctgatcatagcttac[C/T]gcaacctacaactcc | 25909 |
rs2996543 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927069 | tgtagtcccaggtac[C/T]cgggaggctgaggag | 25909 |
rs2996551 | snp | G/T | 0.00914312 | 0.0669923 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839056 | TGCTACAAGGTCCGA[G/T]AATATCATTCATGCG | 25909 |
rs2996552 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839392 | AGCTCTTTATTCATT[C/T]AACAAGTTCATTTAA | 25909 |
rs3063899 | in-del | -/TA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899895 | GAAACTTAGTATTTA[-/TA]TGTTTTATAAAGGAA | 25909 |
rs3067058 | in-del | -/ATTT | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933149 | tttatttatttattt[-/ATTT]gagacggagtctcgc | 25909 |
rs3104111 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923215 | aggtcaggagtttga[A/G]accagcctgactaac | 25909 |
rs3122533 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897148 | GTGTAACTCTGTCTC[A/T]ACTAAAAATAAAAAA | 25909 |
rs4011530 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850876 | AAATGCAGATTTGAC[C/T]AATTTAGTGGGACAC | 25909 |
rs4011531 | in-del | -/TCTTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862720 | AATTTAAGTAATTTA[-/TCTTA]CTAATTGGCACTTTT | 25909 |
rs4130824 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923824 | CCCACACACATGAAG[A/G]ATGTTAGAATTCGA | 25909 |
rs4971277 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927191 | tcaaaaaaaaaaaaa[A/G]aaagaaaTAggccag | 25909 |
rs4971284 | snp | A/T | 0.296619 | 0.245615 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843741 | TATTAAAACATTTGT[A/T]AAAAAAAAAAGTATG | 25909 |
rs4971285 | snp | A/T | 0.296619 | 0.245615 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843742 | ATTAAAACATTTGTA[A/T]AAAAAAAAAGTATGT | 25909 |
rs4971286 | snp | A/G | 0.344147 | 0.231595 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847141 | aaaatacaaaaaaat[A/G]acccaggcgtggtgg | 25909 |
rs4971287 | snp | C/T | 0.361894 | 0.223562 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868670 | TTGGACATGTGCCTT[C/T]AACTGAAATAGGAGT | 25909 |
rs4971289 | snp | A/G | 0.352504 | 0.228019 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869824 | caggcatgaaaacac[A/G]acatccattctgtaa | 25909 |
rs5021094 | snp | G/T | 0.426201 | 0.177351 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842858 | AGACAAGGAATACTA[G/T]AGCCAAACACTGATG | 25909 |
rs6426183 | snp | C/T | 0.303688 | 0.244167 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849422 | ACAGGATTTAAGTCA[C/T]GTTAACCATACTGAA | 25909 |
rs6426188 | snp | A/C | 0.463989 | 0.129263 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930108 | AGCATAAAAAGAAAA[A/C]AAAAGTCTCAAAACT | 25909 |
rs6659764 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889109 | CAAACTACCATAAAG[C/G]CCAGCGTAGTGAAAA | 25909 |
rs6672861 | snp | C/T | 0.298905 | 0.24517 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862436 | agtgagccgagattg[C/T]gccactgcactccag | 25909 |
rs6682729 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918524 | atattggccagatgc[A/G]gaggctcacgccttt | 25909 |
rs6685596 | snp | A/G | 0.312837 | 0.241974 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862467 | cctgggcgacagagc[A/G]agactccgtctcaaa | 25909 |
rs6686324 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902046 | ttacagatggagaaa[C/T]agagctctgaaatgt | 25909 |
rs6688227 | snp | C/T | 0.422 | 0.181428 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847432 | CGATATACAGGAAAA[C/T]GTGAATGGTGATTCT | 25909 |
rs6691158 | snp | C/T | 0.228253 | 0.249052 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869095 | gtgatccgcccgcct[C/T]ggcctcccaaagtgc | 25909 |
rs6694181 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869706 | cctactgttgagaac[C/T]gttcagaaaaaaaaa | 25909 |
rs6694693 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924417 | ATGCAAATTTGTGAT[G/T]TGCTCATTTCAGTAT | 25909 |
rs6696656 | snp | A/G | 0.486984 | 0.079614 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922844 | aaaaaatagccgggc[A/G]tggtggcaggcgcct | 25909 |
rs6700546 | snp | A/C | 0.380138 | 0.213458 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847298 | ccatctcaaaaaaaa[A/C]aaacaaacaaaaaaa | 25909 |
rs7512439 | snp | C/G | 0.0652144 | 0.168387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930291 | gtaggcgcgcgacta[C/G]aggcgccaccaattc | 25909 |
rs7516596 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926425 | CCAGACTTCATCATG[C/G]TGCCTAGCACAAAGG | 25909 |
rs7520969 | snp | A/T | 0.306679 | 0.24349 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845380 | TAAAAAAAAGAAAAA[A/T]AGAGTTGATATCAGA | 25909 |
rs7525627 | snp | C/T | 0.359364 | 0.22481 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856878 | TTATGTATAAAGTAA[C/T]GAACCATTTATAATG | 25909 |
rs7526386 | snp | A/G | 0.431177 | 0.172264 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858568 | ggcacggaggctcat[A/G]cctgtaatcccagca | 25909 |
rs7528980 | snp | A/G | 0.424503 | 0.179021 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845558 | GCTACCTGAAAAAAC[A/G]ATTTATTTCACTTTT | 25909 |
rs7529090 | snp | A/G | 0.429987 | 0.173507 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905930 | TGTAACTGGTCCTAA[A/G]AGTCATATTCAATGC | 25909 |
rs7530860 | snp | A/G | 0.429987 | 0.173507 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854882 | TTCCAACATATCGGG[A/G]GAAATGGGCACAGAA | 25909 |
rs7531694 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906254 | AGCCAGGTACTGCAG[C/G]TATTTCTTTAGGAGC | 25909 |
rs7537256 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925939 | gtgtggtggcgcctg[C/T]ctgtagtcccagcta | 25909 |
rs7542895 | snp | C/G | 0.486398 | 0.0813386 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920627 | tacaaaaaattagcc[C/G]agcgtggtggcgggc | 25909 |
rs7543698 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915492 | TCCCAAATGCTCCCT[A/G]TACTACTATTTTTCC | 25909 |
rs7549408 | snp | C/T | 0.298905 | 0.24517 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845137 | TCACAGTTCATGTTA[C/T]TTCAGCTACTGGGAT | 25909 |
rs7549514 | snp | G/T | 0.433527 | 0.169758 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930163 | TATTTTAGCAACAGG[G/T]TCTCGCTCTGTCACA | 25909 |
rs7550035 | snp | A/T | 0.116838 | 0.211584 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870548 | agacagaatctacAG[A/T]GTTGAAATGATAAAG | 25909 |
rs7550911 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925740 | atgggagaggacccc[G/T]catgaatgggttggt | 25909 |
rs7551797 | snp | C/T | 0.330714 | 0.236612 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905483 | gcctggacaacagag[C/T]gagactctgtctcca | 25909 |
rs7551921 | snp | C/G | 0.403509 | 0.197319 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868988 | tagctgggactacag[C/G]cgcccgccaccatgc | 25909 |
rs7551928 | snp | A/G | 0.449091 | 0.151204 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869002 | ggcgcccgccaccat[A/G]cctggctaacttttt | 25909 |
rs7553684 | snp | A/T | 0.395818 | 0.203069 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902131 | GGCTTAAAAAACCGA[A/T]GCAAAAAAAACTGCC | 25909 |
rs7554747 | snp | A/G | 0.333491 | 0.235646 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869603 | cccttaaaaatgatg[A/G]gaaatctactatgcc | 25909 |
rs9729188 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907972 | AAACACATTCAATTA[C/T]ATAATATTTAAAAAT | 25909 |
rs9729306 | snp | C/G | 0.453331 | 0.145452 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882061 | ggagtgcaatggcac[C/G]atctctgctcactgc | 25909 |
rs9729316 | snp | C/T | 0.453453 | 0.145282 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882232 | tcgatctcctgacct[C/T]gtgatccacccgcct | 25909 |
rs9783081 | snp | A/G | 0.433673 | 0.1696 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853485 | ATAAAACAGAAAAAG[A/G]TAAATTTCACATTTA | 25909 |
rs9783101 | snp | C/G | 0.39979 | 0.200158 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854878 | CCTCTTCCAACATAT[C/G]GGGAGAAATGGGCAC | 25909 |
rs10157601 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898853 | aacacttcgggaggc[C/T]gaggcaggcggatca | 25909 |
rs10436931 | snp | A/G | 0.29278 | 0.246313 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893105 | CATTATTCTCAAAGA[A/G]TAACAAAACTCAATT | 25909 |
rs10558940 | in-del | -/AA | 0.438246 | 0.16451 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866499 | TAACATATGTCCATT[-/AA]ACTACACTCTGTACT | 25909 |
rs10571304 | in-del | -/AAG | 0.0825414 | 0.185628 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843080 | CTCTCACTTTCTAAG[-/AAG]TAGACAACCAGAGAC | 25909 |
rs10635304 | in-del | -/TTTAC | 0.430732 | 0.172731 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854962 | TGATCGGCTTTTTAC[-/TTTAC]ATGTTAGACAATTCT | 25909 |
rs10640263 | in-del | -/GAG | 0.460365 | 0.13508 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910784 | GTCTTTTTCAGAGAA[-/GAG]GAGATTAGATTTTGC | 25909 |
rs10657928 | in-del | -/TATA/TATC/TATCTATC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909079 | ATCTATATATATCTA[-/TATA/TATC/TATCTATC]TATCTATCTATCTAT | 25909 |
rs10666626 | in-del | -/AAAATA/CAAATA | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929411 | ATAAAAATAAAAATA[-/AAAATA/CAAATA]CAGTGAAAACATTGG | 25909 |
rs10682985 | in-del | -/GGT/GTG | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924869 | AACCTAATATAAAGG[-/GGT/GTG]TGTGCATCAATAGGA | 25909 |
rs10802450 | snp | C/T | 0.499954 | 0.00479211 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859779 | GATGGGGTCTCCCTA[C/T]GTTGTCTAGGCTGGT | 25909 |
rs10802451 | snp | A/G | 0.287085 | 0.247234 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864348 | TTAAAAAGAGTTTGC[A/G]TCGTCCTCCTTCCCT | 25909 |
rs10924861 | snp | A/G | 0.360842 | 0.224085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865487 | ATCAGGCTGCTAGAC[A/G]TTTCTTTTCTTCTAG | 25909 |
rs10924862 | snp | G/T | 0.293807 | 0.246132 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872406 | TGGCTAAATAAAAGG[G/T]ATACACCCTTGTCAC | 25909 |
rs10924863 | snp | A/G | 0.347253 | 0.230308 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883476 | CTTCTGATAAAAATG[A/G]AGTGTAAAGTATGCT | 25909 |
rs10924865 | snp | C/T | 0.396 | 0.202938 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918602 | AGAAGTTCGAGGCTG[C/T]GCCTCCAGTGAGCTA | 25909 |
rs10924866 | snp | C/T | 0.325563 | 0.238307 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921569 | CCTAATCAGAATCCC[C/T]CCAAAAATATAGTAC | 25909 |
rs10924867 | snp | A/G | 0.325563 | 0.238307 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921651 | GAGTCAGGAAGTCCA[A/G]TGAATCCTAGGAACT | 25909 |
rs10924868 | snp | A/G | 0.340333 | 0.233109 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927978 | GCACTCCAGCCTGGC[A/G]ACAGAGCAAGACTCC | 25909 |
rs10924869 | snp | A/G | 0.336245 | 0.234652 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928077 | AATCCCAAGGCAGGT[A/G]GATCACGAGGTCAGG | 25909 |
rs10924871 | snp | A/G | 0.0569829 | 0.158885 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931612 | GCGCCGCCGCGGGCC[A/G]AGTCCACCGGGTCGC | 25909 |
rs10924872 | snp | C/T | 0.100588 | 0.200439 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933569 | ATGCCCAGCCTATTT[C/T]TATTTTTGTAGAGAC | 25909 |
rs11340560 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870740 | AGGGTATAAAACCTC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs11370838 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844821 | TTTTTTTTTTTTTTT[-/T]AACTATAGGGCCCCC | 25909 |
rs11396118 | in-del | -/A | 0.499793 | 0.0101816 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919703 | CAAAAAAAAAAAAAA[-/A]TCCTCAAGAGAAGAA | 25909 |
rs11436581 | in-del | -/T | 0.462582 | 0.131564 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892810 | TAATTAAAAAAAAGA[-/T]TTTTTTTTTGGTTTT | 25909 |
rs11576429 | snp | C/T | 0.343254 | 0.231956 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841927 | cagagtagctgggac[C/T]acaggcacccaccac | 25909 |
rs11580065 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920812 | taaaagcatccaggc[A/C]cggtgcctcacgcct | 25909 |
rs11582097 | snp | A/G | 0.381113 | 0.21286 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871729 | TTTTTGAGGCCTCCT[A/G]ACTGCAGACTATAAG | 25909 |
rs11583611 | snp | A/T | 0.431325 | 0.172108 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877923 | TACTGTTATTTATTT[A/T]TTTTTATTTTTTTTA | 25909 |
rs11585265 | snp | A/G | 0.293551 | 0.246177 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903817 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 25909 |
rs11585741 | snp | A/G | 0.453331 | 0.145452 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881817 | CACCCCAGCCTGGGT[A/G]ACAGAGCAAGGCTCC | 25909 |
rs11800847 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858996 | acttgggaggctgag[G/T]caagagaagaggttg | 25909 |
rs11801219 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865259 | AAGTGGCTCACCTGA[C/G]AATAACCAGAAAAGG | 25909 |
rs11805223 | snp | A/G | 0.402277 | 0.198272 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894431 | ACAAAAAAATTAGCC[A/G]AGCGTAGTGGCGGGC | 25909 |
rs11806771 | snp | C/T | 0.350546 | 0.22889 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922839 | tacaaaaaaaatagc[C/T]gggcgtggtggcagg | 25909 |
rs12022495 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896702 | gtacacttgaaatat[C/T]tgaactgcacggtgt | 25909 |
rs12023594 | snp | C/T | 0.344226 | 0.231563 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898164 | ATAGAAAGCTAATAA[C/T]GTGATCCAACCAAAA | 25909 |
rs12023791 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892926 | actgggattacaagc[C/G/T]tgagccaccacaccT | 25909 |
rs12024417 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919601 | acctgtagtctcacc[C/T]actcgggaggctgaa | 25909 |
rs12029050 | snp | C/T | 0.336474 | 0.234568 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874801 | CCAGACACATATCCC[C/T]GAACAACATTAAAAA | 25909 |
rs12031687 | snp | C/T | 0.291235 | 0.246576 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841090 | GAAAAACCTTAGGGA[C/T]TGCTTAGTGCTTTCA | 25909 |
rs12032354 | snp | A/C | 0.338976 | 0.23363 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874715 | ACAATACCAGCCATT[A/C]CAACCTATCCTGAGA | 25909 |
rs12033144 | snp | C/T | 0.360421 | 0.224293 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912439 | AGTGAGCAGGGATTA[C/T]GCCACTGCACTCCAG | 25909 |
rs12033829 | snp | C/T | 0.378568 | 0.214407 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885076 | GGCGCCCCTCCCTTT[C/T]ATTCAAGGTATTTAT | 25909 |
rs12034769 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861600 | CAAGACACACCCTCA[A/G]AAACATATAACTAGT | 25909 |
rs12036689 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926804 | gagattgcagtcagc[C/T]gacactgcaccattg | 25909 |
rs12037780 | snp | A/G | 0.318174 | 0.240525 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897921 | GAGGTTGAGGCTACA[A/G]TGAGCCATGACCATG | 25909 |
rs12048921 | snp | C/T | 0.292266 | 0.246401 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845535 | TACATTCTATAACTC[C/T]CTTCTAGGCTACCTG | 25909 |
rs12061420 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925126 | GAAGTTAACACATTT[C/T]TCCTACTAAACTTAA | 25909 |
rs12065654 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927674 | TTTCCAAAGGCTAGA[C/T]AGGCAGAGCAGGAAC | 25909 |
rs12067009 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874065 | CTGACACAATCACCA[C/T]TAATATTTTATTATT | 25909 |
rs12068067 | snp | A/G | 0.365439 | 0.221752 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862636 | CAGAGCTTTTTATAC[A/G]TAAGTCTACGAAACA | 25909 |
rs12072424 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858812 | ctcaaaaaaaaaaaa[A/T]aataaaTACAAATTT | 25909 |
rs12081100 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892415 | aacctctacctccca[A/G]gttcaagggattctc | 25909 |
rs12088097 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868031 | gcagtggcatgatct[C/T]ggctcactgcaccct | 25909 |
rs12093609 | snp | C/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847150 | aaaaatgacccaggc[C/G]tggtggcaagcacct | 25909 |
rs12093614 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847181 | gtaatcccagctact[G/T]gggaggctgaggcag | 25909 |
rs12094061 | snp | A/G | 0.409891 | 0.192184 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842237 | CTTAATTTCCTTTTC[A/G]TAAAATTAAGGGTCT | 25909 |
rs12096743 | snp | A/C | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894528 | agcctggcgacagag[A/C]aagactcagtctcaa | 25909 |
rs12097543 | snp | G/T | 0.0574049 | 0.161312 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855319 | ACAAAAATGCTCATT[G/T]GATTAAAAAAAAAAT | 25909 |
rs12121733 | snp | C/G | 0.308166 | 0.243139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865910 | CAAAAATCTATAGTG[C/G]TATTTAAAAAATTGA | 25909 |
rs12123173 | snp | C/T | 0.0512217 | 0.151615 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853084 | GTAAAAAATTAATTT[C/T]TTTTACATGAATTTC | 25909 |
rs12126008 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927794 | cggatcacaaggtca[A/G]gagacccagaccatc | 25909 |
rs12126508 | snp | A/T | 0.157642 | 0.232314 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852495 | TAGAATTTTTTTTTT[A/T]AAAAAACTAAGTCTT | 25909 |
rs12127681 | snp | A/C | 0.29789 | 0.24537 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846583 | ATCATCTCATTCTAG[A/C]AGGTGCCTATTTTTA | 25909 |
rs12127941 | snp | C/T | 0.298398 | 0.245271 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841403 | CAATTAGCAAAGATG[C/T]ACAGAATTTCACAAA | 25909 |
rs12129503 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918487 | CAAAATAAAGAAAAA[C/G]TAAAATCTGGTTACa | 25909 |
rs12131776 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890853 | TAAGGAGAAAAATAA[A/G]TGAGGTGGAAGAAAA | 25909 |
rs12133947 | snp | A/C | 0.2776 | 0.248472 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852396 | TTTTTATCCAAATTT[A/C]TATAAATAATTAGAA | 25909 |
rs12134528 | snp | C/T | 0.19238 | 0.243269 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863902 | TAGTTTGATTGTGAA[C/T]GCTAGATGCGTAAAT | 25909 |
rs12239496 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848038 | ATAGGTCTAACCACA[C/T]TTTTCTAACACTGTG | 25909 |
rs12239497 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848110 | AAATTTTCTGAGTGA[C/T]GAGGGGAGAGGAGGA | 25909 |
rs12401831 | snp | C/T | 0.338523 | 0.233803 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842560 | gcactccagccttgg[C/T]gacagaccgagactc | 25909 |
rs12401878 | snp | C/T | 0.343254 | 0.231956 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843012 | AGTTTTATTTTTGAA[C/T]GTTTCCACTGTCTAC | 25909 |
rs12409091 | snp | C/T | 0.324619 | 0.238604 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868945 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 25909 |
rs12410563 | snp | C/G | 0.369481 | 0.219632 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842749 | CTTTTGGCTTTCCCA[C/G]AGTTTCTACTGATTG | 25909 |
rs12567737 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839054 | GTTGCTACAAGGTCC[A/G]AGAATATCATTCATG | 25909 |
rs12691532 | snp | C/G | 0.338296 | 0.233889 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904560 | GTTCAAAGGACAATG[C/G]GGAGTATGGGAAGGA | 25909 |
rs12727818 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859748 | gcccagctaattttt[A/T]tatattttttgtaga | 25909 |
rs12727819 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859749 | cccagctaatttttt[A/T]atattttttgtagag | 25909 |
rs12728345 | snp | A/G | 0.461259 | 0.133677 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869051 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCG | 25909 |
rs12728361 | snp | A/G | 0.372995 | 0.217652 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896958 | CAGGGACAAAACAGA[A/G]ACGTCTGCTACTAAC | 25909 |
rs12733729 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840096 | TTTCCCTTTGTCAAA[C/T]CCTTTGATAAGGTTG | 25909 |
rs12733852 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840136 | AGTGAACCGGTCAAT[A/C]TAACCTGGATTAGTC | 25909 |
rs12739487 | snp | A/C | 0.290201 | 0.246747 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899094 | AACTCCGTCTCAAAA[A/C]GAGAAAAGTATTTTT | 25909 |
rs12739603 | snp | C/T | 0.285519 | 0.247464 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899037 | GAGGTTGCAATGAGC[C/T]GAGATGGTGTCACTG | 25909 |
rs12748665 | snp | A/C | 0.373397 | 0.217424 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875954 | TAGCGAAAGTAGCTA[A/C]ATTTAAGGTGGTTTC | 25909 |
rs12752855 | snp | C/T | 0.371987 | 0.218218 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880159 | GAATTCACTGTGTCA[C/T]CATTCTTAGCTCTTA | 25909 |
rs13374054 | snp | A/G | 0.0241296 | 0.107157 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864132 | CTGTAATCAGAATGC[A/G]CATTTATTGAGTTAT | 25909 |
rs13375572 | snp | C/G | 0.0715223 | 0.175059 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858886 | AATGCTATGAACATT[C/G]TTTTAACAGCTACCA | 25909 |
rs28665436 | snp | C/T | 0.303187 | 0.244277 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848490 | ACAGGCGTGAGCCAC[C/T]GTGACCGGCCAAGTC | 25909 |
rs28805059 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909111 | TATCTATCTATCTAT[C/T]TATATATATATAAAA | 25909 |
rs28833901 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909115 | TATCTATCTATTTAT[A/T]TATATATAAAATTCA | 25909 |
rs34004609 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877054 | CTGAACGCTGGCACT[-/G]GGACTGCAAAAATTT | 25909 |
rs34044345 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923145 | ATAGGCTGGGCACGG[G/T]GGCCCATGCCTGTAA | 25909 |
rs34071076 | in-del | -/A | 0.337386 | 0.23423 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877549 | AAAAGCAAAGTAGAC[-/A]AAAAATTCAAAGAAG | 25909 |
rs34076616 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872097 | CCCAAAAACCTAGGG[G/T]GGTCTCTAACTAAAT | 25909 |
rs34085336 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894183 | TACTCCTGCCTGGGC[-/A]AAAAGTGAGACCATG | 25909 |
rs34089730 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909247 | AACCTCGGCTCTACT[-/A]AAAAAAAAAAAAAAA | 25909 |
rs34199129 | in-del | -/T | 0.457969 | 0.138741 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870076 | TCTTTCATGAATAAC[-/T]TTTGAGGGCTTCAAG | 25909 |
rs34313695 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923004 | AAAAAAAAAAAAAAA[-/A]GTATCAATAGTATTC | 25909 |
rs34350306 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925314 | CACAAAATCCAAAGT[-/C]CCAAAGGATAACACA | 25909 |
rs34357403 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878108 | TAAGTATAAGAATAT[A/C]CAGTAAGAGCCAGGC | 25909 |
rs34394403 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891702 | ATCCATCTAAGACAT[-/G]GGGAAATGTTATTCG | 25909 |
rs34402133 | in-del | -/CTG | 0.343254 | 0.231956 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842867 | TAGAGCCAAACACTG[-/CTG]ATGAATTCAAACTCG | 25909 |
rs34409924 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877144 | TGACAAGTTTACATC[-/G]GGTAAGTAATTACCT | 25909 |
rs34429575 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897608 | CTGTATAGCATGTTA[-/G]CTGTGCTGAATACTG | 25909 |
rs34445530 | in-del | -/TTTAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854963 | TGGGTGATCGGCTTT[-/TTTAC]TTACATGTTAGACAA | 25909 |
rs34452579 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880176 | TTCTTAGCTCTTAAA[-/C]CACTGAAGCATGTAA | 25909 |
rs34452861 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926826 | CACCATTGCACTCCA[-/G]GCCTGGGCAACAAGA | 25909 |
rs34452947 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856173 | TGTCAAGTATTCTGG[-/C]AATATTTTCTATGAA | 25909 |
rs34479116 | in-del | -/A | 0.365646 | 0.221644 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879839 | TCCCCCAACCCCGCC[-/A]AAAAAAAAAGGGAGA | 25909 |
rs34538067 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871241 | CAAACCATGACTCAG[-/T]ACATTAATGGTCTAG | 25909 |
rs34554106 | in-del | -/G | 0.464841 | 0.127841 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904191 | TTTTATAAAAATGTA[-/G]TCCTTTGAAATAATA | 25909 |
rs34589744 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842897 | TCGCCAAATGCAAAA[-/A]TTGACTCCTTTTCTC | 25909 |
rs34595959 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919912 | TGGGAGGCCAAGGCA[-/G]GGAGGATCATGAGCT | 25909 |
rs34617990 | in-del | -/T | 0.452719 | 0.146304 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903663 | TGAGACCCCCCCCCC[-/T]CCGTCTCTGCTAAAT | 25909 |
rs34620309 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839386 | TGTTTAGCTCTTTAT[-/C]TCATTTAACAAGTTC | 25909 |
rs34642893 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857124 | AAGGAGGCAGTGCAC[-/T]TTATCTATATTCCAA | 25909 |
rs34733396 | in-del | -/CTT | 0.347473 | 0.230215 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884325 | CAATCTATTATTAAA[-/CTT]CTTTTCTTCTGCCTG | 25909 |
rs34851364 | in-del | -/A | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838628 | GGGGCGGGGGGAAGA[-/A]CCTCATATAAGGTCA | 25909 |
rs34945773 | in-del | -/AA | 0.433673 | 0.1696 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865761 | TAGTTTAAAGGTTCT[-/AA]GAGAAATCTTTTTAA | 25909 |
rs34997839 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908323 | AATTCACAGGGATAC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs35004695 | snp | C/T | 0.0110026 | 0.07335 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890046 | GCATAACCTTGACAA[C/T]TGCACAGAATCATCT | 25909 |
rs35044246 | snp | C/T | 0.294832 | 0.245947 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922731 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 25909 |
rs35048146 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890079 | ATTTTTAAGAGTTGG[-/A]AAAAAAGCTGGTAAT | 25909 |
rs35049875 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896742 | TCAATAAAGCTGATA[-/T]TTTTGAAAATCACTG | 25909 |
rs35080388 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885919 | GGCTGGGCACGGTGG[-/C]CTCACGCCTGTAATC | 25909 |
rs35083660 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895028 | AGGCCTAATTCCTTT[-/A]AAAAAAAAAAAGGTC | 25909 |
rs35110822 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908724 | AACCCAGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 25909 |
rs35198488 | in-del | -/GAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910785 | TCTTTTTCAGAGAAG[-/GAG]AGATTAGATTTTGCC | 25909 |
rs35199871 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898322 | GGACCTGATTTCTTT[-/A]AAAAAAGTCAAAGTC | 25909 |
rs35224472 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919502 | CGGATCACAAGGTTA[-/G]GGAGATCAACACCAT | 25909 |
rs35320501 | in-del | -/T/TTT | 0.332337 | 0.236052 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911479 | TATCTATGAAGATTC[-/T/TTT]TTTTTTTTTTTTTTT | 25909 |
rs35341079 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913329 | CACAGCTGCCACTCC[-/A]AAAAGCCATCGCAGA | 25909 |
rs35358938 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871800 | GCAGTATAGCTACCT[-/A]AAAGGGTAGCAGTGG | 25909 |
rs35468864 | snp | A/G | 0.0240643 | 0.107019 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931635 | CGGGTCGCCAGGCCA[A/G]GCGCGAGCTCCTCCC | 25909 |
rs35494760 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931003 | TGTTTCCCAGGTAGG[-/A]AAAAGGAAGGCAAAG | 25909 |
rs35511835 | in-del | -/AT | 0.38934 | 0.207568 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899894 | ATTCCTTTATAAAAC[-/AT]ATAAATACTAAGTTT | 25909 |
rs35564406 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875363 | GTCCTCCTTACTTAG[-/A]AAGCCAAATAATAAA | 25909 |
rs35646153 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847477 | TATATACTTCTATTT[-/T]AGAGTTTTCAGTAAG | 25909 |
rs35687457 | in-del | -/A | 0.499539 | 0.0151687 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928323 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs35716055 | snp | A/G | 0.297382 | 0.245469 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901296 | CAGTGAGACGAGATC[A/G]TGCAAGTGCACTCCA | 25909 |
rs35764773 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876784 | AGAATTACGTGGTAA[-/T]TACCCTGTTCCCAAT | 25909 |
rs35779626 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866107 | AGGCTATACTGTCTA[-/C]CCAGTAATGCAAACT | 25909 |
rs35790559 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861174 | ATTTCTTGATGCTCC[-/T]TTTCAGGGCTGTTCA | 25909 |
rs35829086 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886565 | TGACAAGAAAAATGT[-/A]CTGTACATGTTCAGT | 25909 |
rs35881796 | in-del | -/CT | 0.284995 | 0.247539 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889285 | CTCTTCTTTTTTCCC[-/CT]GATTTCCTTTTCTAA | 25909 |
rs35946200 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917702 | TGGGAAGATGGCTAC[-/T]GAAGCTTATATTCAG | 25909 |
rs35982364 | in-del | -/A | 0.375399 | 0.216275 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926047 | TGAGACCCTGTCTTT[-/A]AAAAAAAAAAAAAAA | 25909 |
rs36028619 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863323 | GGAGAAATAAAGCTT[C/T]TGGGTTTCAATCCAG | 25909 |
rs36098218 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899679 | AGAATAGATAACAAA[-/C]CCTATTACACAGCAA | 25909 |
rs36102148 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868630 | AAAAAAAAAAAAAAA[-/A]GTTATTCTTTGTGTT | 25909 |
rs41267533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867405 | GAGCACTGATAACAA[A/G]TGGATGAGATGGGAG | 25909 |
rs41267535 | snp | C/G | 6.61299e-05 | 0.00574983 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891803 | TGATCTCTCGGGCTT[C/G]TGATGCAAAACAGCT | 25909 |
rs41267537 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898438 | GTAAAATTTAAAGAT[A/T]GCAAGTGGAAATTAT | 25909 |
rs41267539 | snp | G/T | 0.000255395 | 0.0112975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931091 | GAACCTCACGGCTGA[G/T]CCCCGAGTCCAACTT | 25909 |
rs41304040 | snp | C/T | 0.303688 | 0.244167 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861389 | ATACCCATACTTTCT[C/T]TGTTGTTTTTACCCA | 25909 |
rs41304042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860702 | GTAAAGACAGGGCCT[C/T]GCTATGTTGACCAGG | 25909 |
rs41304151 | snp | A/G | 0.0527352 | 0.153579 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861024 | TTGGGCTTAGAGGCC[A/G]TGAAAACAGTCTCTT | 25909 |
rs41304153 | snp | A/G/T | 0.0116509 | 0.0754312 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857660 | TTAAACTTCTTTCTA[A/G/T]AAGTATTTGAATTTC | 25909 |
rs41305967 | snp | C/T | 0.00688882 | 0.0582834 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861097 | TCTCATCGGATGTGA[C/T]TGAAACACTGCTGTT | 25909 |
rs41308156 | snp | A/G | 0.0241408 | 0.10718 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849901 | CATCGAAAGTTCCTC[A/G]TTTGGCACTAAAATG | 25909 |
rs41308162 | snp | C/G | 0.194867 | 0.243845 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857783 | CTCTGCTGCAACTAA[C/G]AGATCCTTTGTTTCT | 25909 |
rs41308196 | snp | C/T | 0.0116064 | 0.0752892 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860986 | GTTCAGTTACATTAG[C/T]AGTTAGTGCAGTGGA | 25909 |
rs41310593 | snp | A/T | 0.098322 | 0.19873 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857836 | GTCATACAAATAAGA[A/T]TATTATTTATGCTAA | 25909 |
rs55701948 | snp | A/G | 0.124491 | 0.216211 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879233 | ATAGTGAGACCAAAC[A/G]TATTAAAACTACCAT | 25909 |
rs55703892 | snp | A/G | 0.111224 | 0.207945 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875482 | GCAGAGGCAGGGTTT[A/G]AGAGGAGTGACTCAT | 25909 |
rs55727006 | snp | C/T | 0.350327 | 0.228986 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862229 | CTCACGCCTGTAATC[C/T]CTGCACTTTGGGAGG | 25909 |
rs55783683 | snp | C/T | 0.287867 | 0.247116 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852874 | GGGACTATGGGCACC[C/T]GCCACAGCACCCACC | 25909 |
rs55794479 | snp | A/C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849678 | TGTTTGGTTCAGAAA[A/C/G]GTCCGGCAACAAGAT | 25909 |
rs55889824 | snp | C/T | 0.435119 | 0.16802 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908995 | CCCTCTCATTATTTA[C/T]AGTTTCACTCTCCAA | 25909 |
rs55998210 | in-del | -/AAA | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909421 | AAAAAAAAAAAAAAA[-/AAA]TTTGCATGCTGCTCT | 25909 |
rs56013703 | in-del | -/CTAT/CTATCTAT | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909110 | TATCTATCTATCTAT[-/CTAT/CTATCTAT]TTATATATATATAAA | 25909 |
rs56070865 | snp | C/T | 0.333722 | 0.235565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847499 | TTCAGTAAGTAGGCA[C/T]GTATTGTTTTTGTTT | 25909 |
rs56086758 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854317 | AAAAAAAAAAAAAAA[-/A]TCTGTACATACTTCT | 25909 |
rs56196643 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868771 | CAGAGCAGCCAATAA[A/G]AAAGTACCACGTGAT | 25909 |
rs56224319 | in-del | -/AAG/AG/G | 0.330482 | 0.236691 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930598 | TTTAAAAAAAAAAAA[-/AAG/AG/G]GGGGGGGTCTCGCCA | 25909 |
rs56242683 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868543 | AGAGGTGTGAGCCAC[C/T]GGCCTGGCCTACATT | 25909 |
rs56248647 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839336 | TGCATCCATGTTTAT[C/T]GTGCTACTTGCGCAA | 25909 |
rs56280494 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839994 | TCCTTCACAGCAATA[C/T]TATAAAAATTTGTTC | 25909 |
rs56354817 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893711 | TCAACTTCATCATTT[C/T]TATCAATATGTTAAA | 25909 |
rs56791006 | in-del | -/CT | 0.0584853 | 0.160693 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909435 | AAAATTTGCATGCTG[-/CT]CTGAGTGGTATGATG | 25909 |
rs56797342 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847317 | CAAACAAAAAAAAAA[-/C]TGAAAATGCTCATGA | 25909 |
rs56869109 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856179 | AGTATTCTGGAATAT[C/T]TTCTATGAACTCAGT | 25909 |
rs57125777 | snp | A/C | 0.35894 | 0.225016 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847306 | AAAAAAAAAAACAAA[A/C]AAAAAAAAAACTGAA | 25909 |
rs57201275 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860052 | AGATCACGAGGTCAG[G/T]AGTTCGAGACCAGCC | 25909 |
rs57374813 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916886 | TTTAAACTAGAAGTT[A/T]TGGCAGTTATAAAAT | 25909 |
rs57594834 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860189 | TGCTTGAACCTGGTT[-/G]GGGGGGGGGCGGAGG | 25909 |
rs57811947 | in-del | -/ATGT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884657 | TTTCTCACAGTTACT[-/ATGT]GAGACTGTAATAATC | 25909 |
rs58110440 | in-del | -/AT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846746 | CATATACATATATAT[-/AT]TTTTTGGGGGGATGG | 25909 |
rs58227848 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847316 | CAAACAAAAAAAAAA[-/A]CTGAAAATGCTCATG | 25909 |
rs58383973 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915775 | TTTTAAAAATTGAAT[A/G]GTAATGAATACATTT | 25909 |
rs58495791 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847116 | ACATGGCGAAACCCT[A/G]TCTCTACTAAAAATA | 25909 |
rs58579338 | in-del | -/CTTC/CTTT/CTTTC | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857966 | TAACACTTTCTTCTT[-/CTTC/CTTT/CTTTC]TTTTTTTTTTTGAGA | 25909 |
rs58965522 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899308 | AACTGATACTACTAG[C/T]TGATAATCTCATAAA | 25909 |
rs59221281 | in-del | -/CTTA | 0.37138 | 0.218556 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845965 | TCTAGAACAACACAT[-/CTTA]CTTATTCCCTGGGTG | 25909 |
rs59476689 | snp | G/T | 0.0711525 | 0.174681 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853660 | ACAGAATTACATGAG[G/T]AACATGCAATCTGGG | 25909 |
rs59841568 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847129 | CTGTCTCTACTAAAA[A/G]TACAAAAAAATGACC | 25909 |
rs59904791 | snp | A/T | 0.402277 | 0.198272 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909724 | AATCATAATGTGTGC[A/T]GGGTTCAGTACTAGC | 25909 |
rs59918343 | in-del | -/GTGAGCCGAGATTGCA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854241 | GAGGCGGAGCTTGCA[-/GTGAGCCGAGATTGCA]CCACTGCACTCTAGC | 25909 |
rs59968897 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902067 | TCTGAAATGTTAAGC[A/C]ATTTGTCAAAGGTCA | 25909 |
rs60722674 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847115 | AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT | 25909 |
rs61210171 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847226 | CTCAGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 25909 |
rs61226215 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860197 | CCTGGTTGGGGGGGG[C/G]GCGGAGGTTGCAGTG | 25909 |
rs61465631 | in-del | -/AAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923086 | AGGAGAATGAAGAAG[-/AAG]TTATTTAATCAAATA | 25909 |
rs61562715 | in-del | -/CAAATTTCTATAAATAATTAGAAGAGTTGGTTTTTTATC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852389 | AGTTGGTTTTTTATC[lengthTooLong]TTAAAATTTATTACA | 25909 |
rs61734008 | snp | A/G | 0.00585232 | 0.0537765 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855759 | GCTCTAATTGCAGGG[A/G]TGTAGGTTTCAACAG | 25909 |
rs61734012 | snp | C/T | 0.0082332 | 0.0636303 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877269 | CAACCTATTGCAATG[C/T]TGCCGCAAAAAATTC | 25909 |
rs61853988 | snp | G/T | 0.343254 | 0.231956 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842205 | CTTGTAAATGCCCGA[G/T]AATCTTTTCTGATGA | 25909 |
rs61853990 | snp | A/C | 0.311123 | 0.242413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848866 | AACAAACAACACAAA[A/C]CCCCTACATTTTGTT | 25909 |
rs61853992 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855115 | CATGGGCTCTAGAGT[A/C]AGATAACAACTATGT | 25909 |
rs61853993 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859169 | ATGCTTACTAAGTAA[A/C]GATATCGTAGTCCAA | 25909 |
rs61853994 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860234 | GATCACGCCACTGCA[C/T]TCCAGCCTGGGCAAC | 25909 |
rs61853995 | snp | A/G | 0.293294 | 0.246223 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861905 | TTTTTACTTGTCAGA[A/G]CTAATACATTCTTAT | 25909 |
rs61853996 | snp | C/T | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862255 | GGAGGCAGAGGCAGG[C/T]GGATCACCAGGTCAG | 25909 |
rs61853997 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864818 | GCAGTCCGCAGTCCG[A/G]CCTGGGCGACAGAGC | 25909 |
rs61853998 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865762 | TAGTTTAAAGGTTCT[A/G]AGAAATCTTTTTAAG | 25909 |
rs61854016 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873535 | CATCACAGTGAAGGG[A/C]AAGAATCCGTCCCAA | 25909 |
rs61854017 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876409 | AGCCTTGATTCTTCA[C/G]AATTAATAAAAACAA | 25909 |
rs61854018 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878194 | CTTGAGCCTAGGAGT[A/T]CAAGACCAACCTGGG | 25909 |
rs61854019 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879838 | GTTCCCCCAACCCCG[A/C]CAAAAAAAAAGGGAG | 25909 |
rs61854020 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887421 | CTACGTATATATTTA[C/T]AATAGGTAGCAACAA | 25909 |
rs61854021 | snp | A/G | 0.435407 | 0.167703 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892144 | GAACTCAAATCATCT[A/G]TATCTAGAGCTTGTC | 25909 |
rs61854022 | snp | C/T | 0.399968 | 0.200024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894029 | GGCAATATAGTGAGA[C/T]CATGTCTCTACAAAA | 25909 |
rs61854023 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894215 | CTCAAAAAAAAAAAT[A/T]ACTTTTATCACTTTA | 25909 |
rs61854024 | snp | C/G/T | 0.00442647 | 0.0468369 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894702 | AACCACTTTATTCCA[C/G/T]GTCCATTCAAGAACA | 25909 |
rs61854025 | snp | A/G | 6.61441e-05 | 0.00575045 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246899491 | AAATGAACAACTCCC[A/G]AGTTTAACAAACAAG | 25909 |
rs61854028 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912481 | AGCGAGACGCCGTCT[A/C]CAAAAAAAAAAAACA | 25909 |
rs61854029 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915114 | AGGCAGGTGGATCAC[A/G]AGGTCAAGAGATCGA | 25909 |
rs61854030 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915132 | GTCAAGAGATCGAGA[C/G]CAGCCTGGCCAACAG | 25909 |
rs61854031 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915135 | AAGAGATCGAGAGCA[G/T]CCTGGCCAACAGGGT | 25909 |
rs61854043 | snp | C/T | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919922 | AAGGCAGGAGGATCA[C/T]GAGCTCAAGAGATCG | 25909 |
rs61854044 | snp | C/T | 0.399611 | 0.200291 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922611 | GTTGCCCATGATGGT[C/T]TTGAACTCCTGGGTT | 25909 |
rs61854046 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926998 | GCTAACAAGGTGAAA[C/T]CCCGTCTCTACTAAA | 25909 |
rs61854047 | snp | A/C | 0.5 | 0 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931184 | AGGACAGGCTCAGCA[A/C]GCCGGCCGCTTCCCT | 25909 |
rs61854048 | snp | C/T | 0.343477 | 0.231866 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932175 | TACAAAAAAATCGGG[C/T]CTCTCCGCCTCCGAG | 25909 |
rs66554661 | in-del | -/TATC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909080 | TCTATCTATCTATCT[-/TATC]ATCTATCTATTTATA | 25909 |
rs66680824 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908339 | AAAAAAAAAAAAAAA[-/A]GAGGGGTGGGGCAAG | 25909 |
rs66688318 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872070 | AAAAAAAAAAAAAAA[-/A]GAACCTAGATTCCCA | 25909 |
rs66787763 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865762 | AGTTTAAAGGTTCTG[-/AA]AGAAATCTTTTTAAG | 25909 |
rs67647433 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909267 | AAAAAAAAAAAAAAA[-/A]TTGGCCGCACATGGT | 25909 |
rs68194249 | in-del | -/AAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920166 | AAAAAAAAAAAAAAA[-/AAA]AAGAAAAGAAGCTCA | 25909 |
rs71566675 | in-del | -/T | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884078 | CAAATGAAAAAAAAA[-/T]TTATATGCTGGTTTC | 25909 |
rs71638371 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842582 | CCGAGACTCTGTCTC[A/C]AAAAAAATAAATAAA | 25909 |
rs71638372 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853997 | ACTTTATTGGATACA[A/C]CAATAAAATATTAAA | 25909 |
rs71680437 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843741 | TATTAAAACATTTGT[-/A]AAAAAAAAAAGTATG | 25909 |
rs71792894 | in-del | -/CTGT | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857318 | TGGAAGGAAATAAAA[-/CTGT]CTGTCATCTCCCCTG | 25909 |
rs72504914 | in-del | -/GGT | 0.486266 | 0.0817214 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924868 | TAACCTAATATAAAG[-/GGT]GTGTGCATCAATAGG | 25909 |
rs72764688 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842167 | CTTCAGCAGTGAAAT[C/T]TAACAATGCCAGGGA | 25909 |
rs72764701 | snp | C/T | 0.021333 | 0.101051 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861790 | GCTTAGCCAATGGCC[C/T]TAGTGTTTCTTTCAG | 25909 |
rs72766505 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866972 | CTACTAACAAGCAGG[G/T]AACAAGGAAAGTAAG | 25909 |
rs72766509 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874175 | CTCCAGTTTCTAGTA[C/T]ATACAAGTAGACATG | 25909 |
rs72766511 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875342 | TTGGAGAATCCTCCC[C/T]GGTGTTGTCCTCCTT | 25909 |
rs72766524 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903111 | ATAAAAATGCAACAC[A/G]TAATTCAGGGCCTTT | 25909 |
rs72766526 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904274 | GTAGGAGATATCTTA[G/T]GTAGCAAAGACTGAT | 25909 |
rs72766533 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910693 | GAGCAGATTCTCTCA[C/T]TGTTATAAAGGGGGA | 25909 |
rs72766547 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926524 | TTTAAGACTTTTCCA[A/G]TTTAAGCACACTACA | 25909 |
rs72766549 | snp | C/T | 0.077417 | 0.180873 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927261 | GCCAAGGCGGGAGAA[C/T]GGCTGAGGTCAGGAG | 25909 |
rs72766552 | snp | C/T | 0.0551013 | 0.156571 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932588 | GGGCTCCCAGACTTC[C/T]GGGGAAACGCTTTTT | 25909 |
rs73140260 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846564 | TCTTATCCCTTCCAA[C/T]CCCATCATCTCATTC | 25909 |
rs73142224 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848589 | TCAACTACATGGCTG[A/G]GTGTGGTGGCTCACG | 25909 |
rs73142235 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856780 | CTAGATTTCTCAGGC[A/G]TAAAGCATGTGATTT | 25909 |
rs73142239 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858495 | AATCTAGCTTCACTA[C/T]AGAGTTTGTGTTGTA | 25909 |
rs73142243 | snp | G/T | 0.0707826 | 0.174302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859596 | TCTTTTTGAGACAGG[G/T]TCTCATTCTCTTGCC | 25909 |
rs73142251 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865571 | CCAAACTTGGAAAAC[A/G]GTTTGCTCACTTTTA | 25909 |
rs73142253 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866848 | TAAACGTGCTGCATC[C/T]GAAGCAACACAAGAC | 25909 |
rs73142256 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867034 | CCTGTCCACTAAGCA[A/G]TCTGAAATTATTGAA | 25909 |
rs73144220 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892280 | AAAATCCTTCTTTAA[A/G]TCAAATTCTAATTTG | 25909 |
rs73144222 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894255 | GAAATAATTTTCTTT[C/T]GGGACATCTTCAAAT | 25909 |
rs73144246 | snp | A/T | 0.107694 | 0.205546 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912873 | CTGGGTAATTTCATA[A/T]TGGCTGATAAGGCTC | 25909 |
rs73146606 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923857 | TGAAGTGAAATGAAG[A/C/G]GGGAAATAGATAACC | 25909 |
rs73146640 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930961 | ACCCAAACCAAAACA[A/G]TCAACCAGTGGCAAA | 25909 |
rs74152741 | snp | C/T | 0.0832709 | 0.186283 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839512 | TTTTCAACAAGGCAG[C/T]GTAACATCCATCACT | 25909 |
rs74152745 | snp | A/T | 0.0850919 | 0.187897 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852752 | TCATGAAAACCAGTT[A/T]ATTTATTTATTTATT | 25909 |
rs74152747 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852875 | GGACTATGGGCACCC[A/G]CCACAGCACCCACCT | 25909 |
rs74152748 | snp | C/T | 0.307176 | 0.243374 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855975 | CATTCTGAACAATAA[C/T]ATAAAATTTAAAAGT | 25909 |
rs74152750 | snp | A/C | 0.295599 | 0.245806 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861521 | ATTTTCAGAAGACTA[A/C]AACACAGAACAGGCT | 25909 |
rs74152755 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872698 | AAGCTCCTTCCCATC[A/G]CACTATCATGGGTGC | 25909 |
rs74152756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878906 | GCTTCTCTTACTAGA[C/T]GGTGGAATCATTGTA | 25909 |
rs74163500 | in-del | -/AAA | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878425 | AAAAAAAAAAAAAAA[-/AAA]TACAGTGAAACAATG | 25909 |
rs74163502 | in-del | -/TTTTT | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892302 | TTTTTTTTTTTTTTT[-/TTTTT]GGAGACAGCATCTTG | 25909 |
rs74163703 | in-del | -/CACA | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898661 | ACACACACACACACA[-/CACA]GGAAAACTCCTGCAG | 25909 |
rs74163704 | in-del | -/TA | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899897 | CCTTTATAAAACATA[-/TA]AATACTAAATTTCTT | 25909 |
rs74163708 | in-del | -/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911500 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC | 25909 |
rs74391332 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858371 | TATATACATTAACTT[A/G]CTTAATCCTCAACAT | 25909 |
rs74400921 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882418 | TTTAAAACCCATTAT[C/T]TGTAAATTAAAACTT | 25909 |
rs74407469 | snp | A/G | 0.077417 | 0.180873 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927771 | GTACTTTGGGAGGCC[A/G]AGGCTGGCGGATCAC | 25909 |
rs74456165 | in-del | -/GTGT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923741 | TGTGTGCGTGCATGC[-/GTGT]GTGTGTGTGTGCGCG | 25909 |
rs74473498 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909375 | TGAGCCGAGATTGCG[C/T]CACTGCACTCCAGCC | 25909 |
rs74564494 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868122 | CATGGCCACCAAGCC[C/T]GGCTAATTTTTTTTT | 25909 |
rs74715704 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929491 | AGTATTTAAAAAAGG[A/G]AAGATGGCACTCCAG | 25909 |
rs74784719 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885031 | TCAATGTTGTCAACT[A/G]GCAACAAATATAACT | 25909 |
rs74824937 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878743 | AGCAAATGGTACCCA[A/C]TGTTGGCAGATCAGG | 25909 |
rs74951703 | snp | C/T | 0.404733 | 0.196361 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910570 | CTTGAATTTGGGTGA[C/T]GGGTTTATGGGAACT | 25909 |
rs74997643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896481 | TATTTGACCCATTTA[C/T]ATGAAATGTCTAGAA | 25909 |
rs75044729 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847317 | CAAACAAAAAAAAAA[A/C]TGAAAATGCTCATGA | 25909 |
rs75046282 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857483 | CTGCCTCAATTTACC[A/G]TGTCTCTGTATATTT | 25909 |
rs75082575 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872053 | GAACTATTAATGACA[A/C]AAAAAAAAAAAAAAA | 25909 |
rs75099827 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895389 | TTCTCAAATGGTTCT[A/G]AACAGACAATATGCG | 25909 |
rs75100583 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865163 | AGGTCACTCTCTTCT[C/T]GATTTCCTAATAAAC | 25909 |
rs75147128 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914416 | AGTTGTTTCAGGCTG[G/T]AACTTACTACAGACA | 25909 |
rs75175259 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848862 | CTCAAACAAACAACA[A/C]AAACCCCCTACATTT | 25909 |
rs75206771 | snp | A/C/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910612 | CTAACTATCTGAAGA[A/C/T]GTCTGAAATCTTCAA | 25909 |
rs75217552 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920164 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAGCT | 25909 |
rs75244123 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868735 | CAAATCTTCTAAGAA[A/G]GGCTTACATTTCTTG | 25909 |
rs75306832 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922421 | CAGTATTCTGTTGCG[C/G]TTTTTTGGGTTGTTT | 25909 |
rs75319018 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870444 | AAACAAAAACAGACT[A/G]AAGATGTGATGAATT | 25909 |
rs75328986 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847309 | AAAAAAAACAAACAA[A/C]AAAAAAACTGAAAAT | 25909 |
rs75330127 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864997 | ACTACAAGGTTTTCC[A/G]TAATGTCCTAGTCCC | 25909 |
rs75378536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913109 | TACCTTTTTTTTTTT[A/T]ATAGATAGGAAGATA | 25909 |
rs75379026 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930598 | GTTTAAAAAAAAAAA[A/G]GGGGGGGTCTCGCCA | 25909 |
rs75404843 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844279 | TAATCCTATATGTAA[C/T]CTGAGCTAGTCTGTG | 25909 |
rs75524158 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881850 | CTCAAAAAAAAAAAC[A/C]AAAAAAAAAAACAAA | 25909 |
rs75564165 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841297 | AATACTGCTGGATTA[A/C]AAGGACGGGCCGAGT | 25909 |
rs75744500 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851623 | AATCAGACTTTCTCA[C/T]TCAGTCAAAATAACT | 25909 |
rs75810554 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920747 | TGCACTCCAGCCTGG[A/G]TGACAGAGCAAAACA | 25909 |
rs75856586 | snp | C/G | 0.108048 | 0.20579 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901317 | GTGCACTCCAGCCTG[C/G]GCGACAGTGAGACCC | 25909 |
rs75856974 | snp | C/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932840 | ATACTAAGTAGTAAG[C/T]AAAAGGATTATAACA | 25909 |
rs75891732 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921693 | GAAATGACTCAACAA[C/T]AGTAGTAGAAACCGC | 25909 |
rs75942303 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900901 | AGAAGGACTTATCCA[A/G]TTATAAGGTAAAGAG | 25909 |
rs76041954 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918682 | TAAAAACAAATGACA[C/T]GCATCTGGGACCAAG | 25909 |
rs76119999 | snp | A/G | 0.000185401 | 0.00962634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907512 | GCTATATGCAAAAAA[A/G]CTACCTATAATCAAA | 25909 |
rs76213609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844858 | AAAGCAATTATCAAT[A/G]TAATTACAGACGAGC | 25909 |
rs76243060 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922423 | GTATTCTGTTGCGGT[G/T]TTTTGGGTTGTTTTT | 25909 |
rs76250599 | snp | C/T | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846979 | CAGGCTGGTTGGATT[C/T]TGAAGAATATTTAAG | 25909 |
rs76289950 | snp | A/G | 0.077417 | 0.180873 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928258 | CAGTGAGCCGACATC[A/G]CGCCACTGCACTGTA | 25909 |
rs76320352 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917087 | TCAGTAACTATCTGA[C/T]TTATGCATGTTTTTA | 25909 |
rs76330535 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855020 | GTATTACCTTAATCA[C/T]GGGACAAAAACTAGT | 25909 |
rs76348162 | snp | C/T | 0.00422183 | 0.0457503 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877144 | CTGACAAGTTTACAT[C/T]GGTAAGTAATTACCT | 25909 |
rs76526962 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906770 | CAAATTAACTTAGCT[A/T]CAAAGTATCAATATA | 25909 |
rs76539569 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919727 | AAAAAATCCTCAAGA[A/G]AAGAATTTATTATCA | 25909 |
rs76559260 | in-del | -/TTATA | 0.398714 | 0.200958 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875041 | TGACAGGCCAACAAC[-/TTATA]TTATAGATAAACCAG | 25909 |
rs76579350 | in-del | -/GG | 0.185788 | 0.241613 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860197 | TGCTTGAACCTGGTT[-/GG]GGGGGGGGCGGAGGT | 25909 |
rs76581262 | snp | C/G | 0.0618563 | 0.164627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878604 | TTCTGAAGATATACA[C/G]TAAGAATGGTAATGA | 25909 |
rs76803337 | in-del | -/ACAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853776 | TTTAGTGTTTAACAA[-/ACAA]CAACAAAACATCAAT | 25909 |
rs76890750 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903853 | AAAAAAAAAAAAAAA[A/G]AGAATCACTTTTCAA | 25909 |
rs77050095 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929489 | TGAGTATTTAAAAAA[A/G]GAAAGATGGCACTCC | 25909 |
rs77068184 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880570 | GAGACTCCAGCTCAA[A/C]AAAAAAAAAAAAAAA | 25909 |
rs77098280 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881848 | GTCTCAAAAAAAAAA[A/C]CCAAAAAAAAAAACA | 25909 |
rs77164384 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908089 | AATTTAGAACTACTA[C/T]CTAAATACCTTCCTT | 25909 |
rs77210882 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871029 | GTAGCCTTGCTTAAG[G/T]TGCCAAACCTTTTGA | 25909 |
rs77241159 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849061 | TTTGGGGAGAGATCA[A/C]CCCTGTTGAGAAGCT | 25909 |
rs77251069 | snp | G/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892327 | TTTTTTTTTTTTTTT[G/T]TTTTGGAGACAGCAT | 25909 |
rs77279727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909613 | ACAGCCTCAAAGCAC[A/G]AGAGTGGTCATGCTG | 25909 |
rs77343062 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933432 | CCACCGCGCCCGGCC[C/T]TATTTTTTATTTTTT | 25909 |
rs77346208 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903839 | CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 25909 |
rs77485059 | snp | A/C/T | 0.00496204 | 0.0495627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904050 | TGAAACAGAAATTAA[A/C/T]GAAGACACGCTAAAT | 25909 |
rs77522965 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922420 | ACAGTATTCTGTTGC[G/T]GTTTTTTGGGTTGTT | 25909 |
rs77580733 | in-del | -/AT | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838827 | GTTTCCCTTACTACT[-/AT]GATACTAAGTATCTG | 25909 |
rs77627517 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903795 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 25909 |
rs77637621 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903179 | ATTAGGTTCAGAAAA[C/G]TCGGTTCTAGAGACA | 25909 |
rs77651496 | snp | A/C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903663 | TGAGACCCCCCCCCC[A/C/T]CCGTCTCTGCTAAAT | 25909 |
rs77666704 | in-del | -/TT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913108 | ATACCTTTTTTTTTT[-/TT]ATAGATAGGAAGATA | 25909 |
rs77746851 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857967 | TAACACTTTCTTCTT[C/T]TTTTTTTTTTGAGAT | 25909 |
rs77823298 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862850 | AATTATGTATCAGAA[G/T]CCTCTGAAGATTTCG | 25909 |
rs77855548 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931052 | TATTTTAAATCTCCT[A/T]GATCTGACCAATCGG | 25909 |
rs77886043 | snp | A/G | 0.298651 | 0.24522 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848270 | CCGGGCTGGAATACA[A/G]TGGCACAATCTTGGA | 25909 |
rs77945508 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899128 | AATTCTTTTTTTTTT[C/T]CCTGTGCCAGGCACT | 25909 |
rs77966128 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913587 | CTATACTAGGAATTA[C/T]ACCATTACTCAATAC | 25909 |
rs77970420 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856084 | AGTAGAAATGAAATG[A/G]TTTTAAAATGCCTGT | 25909 |
rs78105842 | snp | A/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912325 | ACTAAAAAAAAAAAA[A/T]TACAAAAATTAGCCA | 25909 |
rs78140908 | snp | G/T | 0.5 | 0 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838988 | TGTTTACCTTACTAC[G/T]ATGATACTAAGCACC | 25909 |
rs78228621 | snp | A/T | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894213 | GTCTCAAAAAAAAAA[A/T]TTACTTTTATCACTT | 25909 |
rs78465670 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868891 | GCTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGTG | 25909 |
rs78487876 | in-del | -/A | 0.380919 | 0.21298 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929491 | AGTATTTAAAAAAGG[-/A]AAGATGGCACTCCAG | 25909 |
rs78510255 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931000 | TCCTGTTTCCCAGGT[A/G]GGAAAAAGGAAGGCA | 25909 |
rs78518852 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880876 | ATGCTAGGAAGAACA[A/G]TAAGAAAATTAATTT | 25909 |
rs78528395 | in-del | -/AAAA | 0.422158 | 0.181278 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848862 | AACAAACAACACAAA[-/AAAA]CCCCCTACATTTTGT | 25909 |
rs78531048 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866922 | ACCCAAGATTAATCT[A/G]TAATTAAGTATAAAA | 25909 |
rs78575465 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924850 | CAAAACAGATCCAAA[A/C]GTCTAACCTAATATA | 25909 |
rs78575640 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851522 | CAGGTTTTTGATGAC[C/T]CTTGGCTGTGTGCCT | 25909 |
rs78646281 | snp | A/G/T | 0.00222436 | 0.0332756 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843966 | TATCTGTATCTTTAT[A/G/T]TATGTGTGTATATAT | 25909 |
rs78735541 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892332 | TTTTTTTTTTTTTTT[A/G]GAGACAGCATCTTGC | 25909 |
rs78735882 | in-del | -/G/GGG/GTG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924867 | CTAACCTAATATAAA[-/G/GGG/GTG]GGTGTGCATCAATAG | 25909 |
rs78752151 | snp | A/G | 0.000112581 | 0.00750185 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853334 | ATTTTTTACATTTAA[A/G]CTGAAAAATAAATCC | 25909 |
rs78818563 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871101 | AGCACTTACCCAAAT[A/G]CTAGGACCACTAAAA | 25909 |
rs78841711 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901626 | CTCAAAAAAACAAAA[C/G]AAAAAAAAACAAAAC | 25909 |
rs78844199 | snp | C/T | 0.444444 | 0.157135 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918875 | CCACCACCATCCTCC[C/T]TACAGAAAAAAGAAA | 25909 |
rs78905536 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903837 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 25909 |
rs78952582 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928738 | AGTTCAACAATTATA[C/T]TGCAACATGTACCAA | 25909 |
rs78998889 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862480 | GCAAGACTCCGTCTC[A/C]AAAAAAAAAAAAAGT | 25909 |
rs79021188 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903840 | GAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAAG | 25909 |
rs79053065 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872984 | AACTGTTTGGACCAT[A/G]TATTATTAAGCACTC | 25909 |
rs79067339 | snp | C/T | 0.384209 | 0.210922 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929550 | GAGTGGAAACATCTC[C/T]TCCACAGAATGAGTC | 25909 |
rs79212166 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888948 | TGACCCTAGTTAGCA[C/T]GATGAGAACTACAGA | 25909 |
rs79322666 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897819 | GACCCTGTCTCTACC[A/C]AAAAAAAAAAGGGCT | 25909 |
rs79326084 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853683 | AATCTGGGCTTTGAT[A/G]CAACTAGGATAAAGA | 25909 |
rs79369288 | snp | C/G | 0.302435 | 0.244439 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858257 | AGCCACTGCACCCGG[C/G]CAACACCTTCTTCTT | 25909 |
rs79453909 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853988 | AGTATACAAACTTTA[C/T]TGGATACAACAATAA | 25909 |
rs79531849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842640 | AGTAGGGTGGGGACA[C/G]AGCGAGACTGTCTCA | 25909 |
rs79618149 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879592 | ACTTTGGGAGACCGA[A/G]ACAGGTGGATCAATC | 25909 |
rs79709415 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880567 | AGTGAGACTCCAGCT[A/C]AAAAAAAAAAAAAAA | 25909 |
rs79921823 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930573 | ATCAGTGAAAGCTCA[A/C]AAAAAAACAGTTTAA | 25909 |
rs80056231 | snp | G/T | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931053 | ATTTTAAATCTCCTT[G/T]ATCTGACCAATCGGG | 25909 |
rs80110842 | snp | A/G | 0.165853 | 0.235413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846044 | CAGAAGGAAGTAAAA[A/G]TACCTACACTTTACT | 25909 |
rs80123663 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887012 | CCTTCTTTAAACAGT[A/G]AGAAACCTGGGGTTC | 25909 |
rs80176342 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928304 | CGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 25909 |
rs80176396 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878082 | AAACACCAGCAAAAA[C/T]TGCAAAAGATTAAGT | 25909 |
rs80254162 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874308 | ACATTAACTATTAAA[C/T]GTCTCTATCTTCAGA | 25909 |
rs80260655 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912483 | CGAGACGCCGTCTCC[A/C]AAAAAAAAAAACAAA | 25909 |
rs80329222 | snp | A/C | 0.277867 | 0.248442 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847296 | CTCCATCTCAAAAAA[A/C]AAAAACAAACAAAAA | 25909 |
rs111306674 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910314 | AACTGTCAAATGCAA[C/T]TAATGTGCAGACTGT | 25909 |
rs111386980 | in-del | -/TTCT/TTCTT/TTT | 0.0596104 | 0.162024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857964 | GCTAACACTTTCTTC[-/TTCT/TTCTT/TTT]TTTTTTTTTTTTTGA | 25909 |
rs111449141 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875590 | AAATTGACATGGCCA[A/G]CTTCACTGTGTCATC | 25909 |
rs111487016 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922477 | GTCACCCAGGCTGGA[A/G]TGCAGTGGCATTATC | 25909 |
rs111550056 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840775 | TCTGATGACTTTACA[A/G]ATAGGTGTACATTAA | 25909 |
rs111560082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889377 | TAGATGTCCTGCACA[C/T]ACTATTTTATTTAGC | 25909 |
rs111560856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862340 | AAAAAATTAGGCAGG[C/T]GGGGTGGCGGGCGCC | 25909 |
rs111561029 | snp | A/C/G/T | 7.93106e-05 | 0.00629682 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876175 | TCTCCCGCAAACGAG[A/C/G/T]ATCACGATCATTCTA | 25909 |
rs111574615 | in-del | -/TACA | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864517 | AAATATCCATTCACC[-/TACA]TACATGTAATATATA | 25909 |
rs111639204 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910784 | TGTCTTTTTCAGAGA[A/G]GAGATTAGATTTTGC | 25909 |
rs111704204 | snp | A/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866496 | GTTTAACATATGTCC[A/T]TTAAACTACACTCTG | 25909 |
rs111707702 | snp | A/C | 0.299411 | 0.245069 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847297 | TCCATCTCAAAAAAA[A/C]AAAACAAACAAAAAA | 25909 |
rs111713548 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886823 | GAATAAAAGCTTTAT[A/T]AAAAACCTGATACCT | 25909 |
rs111742720 | snp | A/C | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919605 | GTAGTCTCACCTACT[A/C]GGGAGGCTGAAGCAG | 25909 |
rs111745834 | snp | C/T | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899606 | GACTGCAAGGCAAGG[C/T]GTCAAATTATTACAT | 25909 |
rs111766571 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856396 | CAACAAATAGTATTT[A/G]AAAGTAAATTCAATA | 25909 |
rs111792872 | snp | A/G | 0.0315348 | 0.121544 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853057 | AACCAAAACTGAAAG[A/G]CTGATAAAGAAGTAA | 25909 |
rs111800702 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856341 | ATTCTAATCTGACCT[C/T]TCTCAAAACCCAATT | 25909 |
rs111816815 | snp | C/T | 0.305685 | 0.24372 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847624 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGACCA | 25909 |
rs111820215 | in-del | -/AAAAAT/AAAAATAAAAAT/AAAAT | 0.515779 | 0.113064 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929410 | GAGACTCCGTCTCAA[-/AAAAAT/AAAAATAAAAAT/AAAAT]AAAAATAAAAATAAA | 25909 |
rs111824048 | in-del | -/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847309 | AAAAAAACAAACAAA[-/C]AAAAAAACTGAAAAT | 25909 |
rs111836067 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844461 | TGCAGTGGCTCACAA[C/T]TGTAATTCCAGCACT | 25909 |
rs111878868 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894467 | AATGGCGTTTGAACC[C/T]GGGAGGTGGAGCCTG | 25909 |
rs111882101 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857998 | GGAGTCTTGCTGTGT[C/T]GCCCAGGCTGGAGTG | 25909 |
rs111892942 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915245 | TAAGGCAGGAGAATC[A/G]GTTGAACCCGGGACA | 25909 |
rs111926413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929169 | ATCCCAGCACTTTGG[C/T]TGGCCGAGGTGGGCA | 25909 |
rs111966101 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846864 | TCAAGCCATCCTCAC[A/G]CCTCAGCCTCCCAAG | 25909 |
rs111980491 | snp | C/T | 0.252421 | 0.249988 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922809 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 25909 |
rs111986753 | snp | A/G | 0.243061 | 0.249904 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869046 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGATGG | 25909 |
rs112063894 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847915 | CCACTCCCTGCCAAT[A/G]AAATGTTTTTCATTT | 25909 |
rs112161335 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868152 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTA | 25909 |
rs112172408 | snp | A/C | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916372 | GTTGTGGACCACAAG[A/C]CAAGCAAGCAAGTCC | 25909 |
rs112185957 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922102 | CAGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT | 25909 |
rs112266039 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884196 | AACTACAATTTTGAT[C/G]TCATAAAAAATCTCA | 25909 |
rs112314625 | in-del | -/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890105 | GTAATAATCCCCAAA[-/T]ATCTCAACAATACAT | 25909 |
rs112327310 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929890 | AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA | 25909 |
rs112419962 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869889 | AATTTAGAAATACAT[C/T]TCATAAAGCTATAGC | 25909 |
rs112432982 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881961 | CTGGGATTACAGGCA[C/T]GAGCCACCGTGCCTG | 25909 |
rs112436963 | snp | A/C | 0.000368942 | 0.013577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887164 | ATGTGTATTTTCTAA[A/C]ATTCTAGTAATTCAT | 25909 |
rs112457059 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932500 | CGGAGTCTTGCTCTG[C/T]TGCCCAGGCTGGAGT | 25909 |
rs112484454 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906412 | TGAAAATCCGTCTCT[-/A]AAAAAAAAAAAATAC | 25909 |
rs112496509 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868127 | CCACCAAGCCCGGCT[A/C]ATTTTTTTTTTTTTT | 25909 |
rs112498177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861458 | ATTCTCTTCTAGTAC[A/G]TAAAAGTTAATGGTG | 25909 |
rs112511665 | in-del | -/AGAA | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919360 | CTGAGTCTCTTACTC[-/AGAA]AGACAACATTTTCTT | 25909 |
rs112539534 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926609 | ACCTGTCATCCCAGC[A/G]CTTCGGAAAGCTGAG | 25909 |
rs112542991 | snp | A/G | 0.300673 | 0.244811 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869087 | CTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC | 25909 |
rs112588849 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869585 | ATTCCAAAATTCCTA[A/C]GGCCCTTAAAAATGA | 25909 |
rs112595233 | in-del | -/GTT | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885343 | ATGAACACTGTATTT[-/GTT]TCAATCTGAATTTGA | 25909 |
rs112612636 | snp | C/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888478 | TCCTAACTGAGAAAC[C/G]AGTCCATCAATCATC | 25909 |
rs112613828 | snp | A/G | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920353 | AGGAAAAATCAAGTA[A/G]ATTTGAAAAAATTTC | 25909 |
rs112636616 | snp | A/G | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915882 | GAGTATCAGAACATT[A/G]CATGTCATTGCTATT | 25909 |
rs112684992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875571 | CTCTAGTGGAAGGAA[A/G]AGTAAATTGACATGG | 25909 |
rs112724110 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912925 | TTATTCCAGCATTTA[C/T]TTAAGAATAGATCTT | 25909 |
rs112802786 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865766 | TTAAAGGTTCTGAGA[A/G]ATCTTTTTAAGGTAT | 25909 |
rs112820496 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925526 | CTGGGAAGCTCAGGC[A/G]GAAGGATCTCTTAAG | 25909 |
rs112848017 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869005 | GCCCGCCACCATGCC[C/T]GGCTAACTTTTTCTA | 25909 |
rs112857397 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858800 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAT | 25909 |
rs112900823 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926374 | TCTTCCTCCCTTTCA[C/T]ATCCAAGCTTCTAGA | 25909 |
rs112922854 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914556 | ATAAATACTAAAGCA[A/C/T]ATTCAATTCCTCAGT | 25909 |
rs112927817 | snp | A/C/T | 0.0150695 | 0.0854849 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852494 | ATAGAATTTTTTTTT[A/C/T]AAAAAAACTAAGTCT | 25909 |
rs112933647 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862804 | AGTGTTTCAGAAAAA[A/G]AATTTCGTCACACGA | 25909 |
rs112962898 | in-del | -/CATTTCTAT | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900600 | TGATTCATCAAAACG[-/CATTTCTAT]CATTTGTATGTAAGA | 25909 |
rs113045510 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897717 | TGGGCAAGGTGGCTC[A/G]TGCCTGTAATTTCAG | 25909 |
rs113069655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882800 | ACGTAAAACAGCCAC[A/G]CCACAGTTGTGATGG | 25909 |
rs113072253 | snp | C/T | 0.15698 | 0.23205 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869012 | ACCATGCCTGGCTAA[C/T]TTTTTCTATTTTTAG | 25909 |
rs113113662 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842194 | GGGAGCCAGTGCTTG[C/T]AAATGCCCGATAATC | 25909 |
rs113177866 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931266 | GTCGCGGCCCCGGCC[A/G]TCCGTAAAGGGACCC | 25909 |
rs113177890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887649 | TACAAGAAACAAAGA[C/T]ATACGCAAATTTCTA | 25909 |
rs113198494 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902368 | ATAGCAATCTGGAGA[A/G]CAAGAAATATCTAGT | 25909 |
rs113201284 | in-del | -/ACAAAAA | 0.413748 | 0.188909 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848707 | GCTGTCTCTACAAAT[-/ACAAAAA]ATTAGCCAGGCCTGT | 25909 |
rs113211697 | in-del | -/AT | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913110 | ACCTTTTTTTTTTTT[-/AT]AGATAGGAAGATATC | 25909 |
rs113318350 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847848 | CACTTTTGGTGGTTA[C/T]TATATTCCTCCAGGT | 25909 |
rs113330099 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900673 | AATTTTAAGGCCTTA[C/T]TAAAAAGTAGTCACT | 25909 |
rs113331100 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922054 | TTAGACTTTGTTACA[C/T]ATCCATGTTGAAAAC | 25909 |
rs113355017 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849062 | TTGGGGAGAGATCAC[C/T]CCTGTTGAGAAGCTC | 25909 |
rs113415158 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862652 | TAAGTCTACGAAACA[A/T]AAAACTGCATCCATC | 25909 |
rs113479413 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867305 | CCTCAGGCAGCTCTG[A/G]AGCTGGGAGCGAATA | 25909 |
rs113480627 | snp | A/G | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888376 | ACTCTAAATGATAGC[A/G]CATTACTGCAAACCT | 25909 |
rs113481315 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906711 | GGAGAAACAAATAAA[C/T]TGACAACTTAAGGGC | 25909 |
rs113491073 | in-del | -/A | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869712 | TTGAGAACTGTTCAG[-/A]AAAAAAAAAAAAGTC | 25909 |
rs113507273 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875533 | TAAAATGCTATCAAA[C/T]GGTATCACATGCTAC | 25909 |
rs113530301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878214 | ACCAACCTGGGCAAC[A/G]TGGTGAGACCCTAAC | 25909 |
rs113530654 | snp | C/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903694 | ATACAAAAAAATTAG[C/G]CAGGCGTGGTGGCGG | 25909 |
rs113617117 | snp | A/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864597 | CTAGACTGACTTGGG[A/T]GGCCGAGGCGGGTGG | 25909 |
rs113656994 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869086 | CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC | 25909 |
rs113703954 | snp | A/G | 0.5 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846525 | CTAGTAAGTGGCAGA[A/G]ATGAGAGATCTCAAT | 25909 |
rs113715626 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896990 | TTATTACCTATAGTT[C/T]ATAGAAGTTCTACCA | 25909 |
rs113767945 | snp | A/C/T | 0.00152939 | 0.0276115 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853227 | TCCTGGTTAAGCCTG[A/C/T]GCTCAGAGACAATAG | 25909 |
rs113926329 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927102 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 25909 |
rs113929196 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870978 | TTCGAAAAACTAAAA[A/C]CAACCAAGCAAACAA | 25909 |
rs113949515 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869661 | ATGAAAACACATCTG[C/T]TGACAGCATGGTTTA | 25909 |
rs113957278 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868930 | GCTCACTGCAAGTTC[C/T]GCCTCCCGGGTTCAC | 25909 |
rs114053005 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857556 | ACTAAACTTCTTTTA[A/G]AACAGCCAACATTAC | 25909 |
rs114060363 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919871 | TCACAGAGCCAGGCA[A/G]GGTGGCTCATGCCTG | 25909 |
rs114075145 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893321 | CTAGAAAGCGCCATG[C/T]CTTCCTAACGAACTT | 25909 |
rs114114245 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864245 | AGTCAAGTATATTAA[C/T]GTAATCCAAAGTGCT | 25909 |
rs114177404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875578 | GGAAGGAAGAGTAAA[G/T]TGACATGGCCAACTT | 25909 |
rs114248509 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841515 | TGTGCTTTTATTGAA[C/T]TCAACCATGCCTACT | 25909 |
rs114316927 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853543 | GAAACATTAATATGA[A/C]GACCAACTGCTTCAA | 25909 |
rs114321813 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876855 | TAATGCTAGGCACAG[C/T]GGTTACCAAACTGTA | 25909 |
rs114419014 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915476 | TAAATCAAGTCTAGT[A/T]TCCCAAATGCTCCCT | 25909 |
rs114426926 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856378 | TGCTAATTTTGAAAA[C/T]TACAACAAATAGTAT | 25909 |
rs114433508 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908610 | CAAGAATCTTAGGCC[A/G]GGCACGGTGGCTCAC | 25909 |
rs114463419 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884714 | ACTGATTAGAGAACA[C/T]TAAAATCTGCAAAAG | 25909 |
rs114581620 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848977 | TGTTTAAAGCACCCC[C/T]TATTAAAATTTTATT | 25909 |
rs114583882 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861607 | CACCCTCAAAAACAT[A/G]TAACTAGTTAGAAAC | 25909 |
rs114629300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884828 | TGAGGATGCAATAGG[A/G]CAAATGCAATGACAA | 25909 |
rs114659015 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851791 | AAAAAAATTAACCGG[A/G]AAAAACAGAAACAAC | 25909 |
rs114666220 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847509 | AGGCATGTATTGTTT[C/T]TGTTTTGAGACGTGG | 25909 |
rs114685372 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892755 | TCCTAGCTCAGCCTC[A/C]CAAGGAGCTGGGACT | 25909 |
rs114713118 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897436 | AATTGCATTTTTCCA[C/T]ATAGCCATGTGTTGC | 25909 |
rs114716257 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869660 | GATGAAAACACATCT[A/G]TTGACAGCATGGTTT | 25909 |
rs114745981 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872921 | TATTAACCTAGAGAC[C/T]GGGTTCACCTTAAGA | 25909 |
rs114757176 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869241 | GTGTACTTACTCCAC[C/T]GACTAACTGTTCCCC | 25909 |
rs114761567 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843230 | GCCATTTACTCTGTT[C/G]GGAGGAATGCCTGTC | 25909 |
rs114766348 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895666 | TTTGTCAGATCATCA[C/T]ACTGTGGGCAAACGT | 25909 |
rs114777821 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882299 | ACCGCACCTGGCCTA[G/T]TATTACTTTTAAACA | 25909 |
rs114778821 | snp | A/G | 0.000133236 | 0.00816089 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931144 | TGTGGCCAGGCCCAA[A/G]CGCATGTGGAACACA | 25909 |
rs114799044 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887820 | AGGTAGTATCACGCT[A/G]ACTTATAATGTATTC | 25909 |
rs114875965 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848207 | GGCTCAAACTGTATC[A/G]GTACAACAAGTCATC | 25909 |
rs114876655 | snp | C/T | 0.0228335 | 0.104381 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899949 | TAAGTTATCCATATG[C/T]TAACTAACAGTGAGA | 25909 |
rs114881438 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885791 | AAGACTCGTTTAAAT[A/G]TAAGCTGAAAAAATC | 25909 |
rs114916491 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921774 | TATATATTACTGAAA[C/G]GATCCTTAACAAATA | 25909 |
rs114984756 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883634 | ACTTTCTAGCAACCC[A/T]GAAGTCATTCTCTAT | 25909 |
rs115056064 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902900 | CAAGTCTTCTAAAGT[C/T]ATTTAACACAGAAGC | 25909 |
rs115067616 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925879 | ATTTGACACCAGCCT[A/G]GGCCACATGGCGAAA | 25909 |
rs115119240 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882481 | AATGAAAATTTAAAG[A/G]TACTTAGAACAGAAT | 25909 |
rs115125951 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879440 | ATTTTATTCTATAAA[C/T]TGGCACATGTGCATT | 25909 |
rs115134012 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932093 | GGAATTTTCAAACTC[C/T]CGGTGAAAGAAGGAG | 25909 |
rs115153060 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861629 | GTTAGAAACAACACA[A/G]TATAAGGTAAAAACA | 25909 |
rs115162821 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857188 | TGACACTCTCACCAA[G/T]CTGCTTGACCATACT | 25909 |
rs115165967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853768 | TTAAAATCCTTTAGT[A/G]TTTAACAACAACAAA | 25909 |
rs115370486 | snp | A/T | 0.000870038 | 0.020839 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899548 | ATAATCCACTTACAT[A/T]TATTTAAAATGGCAT | 25909 |
rs115371557 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871074 | AAAAGGCAGGGAACA[C/G]CTAGCCAGGGGAGCA | 25909 |
rs115409554 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891487 | AAAATTTATGAGTTC[C/T]TTGAATAAAAAATAC | 25909 |
rs115444277 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872454 | AGGTGGTCAGAGCTT[C/T]ACTCAAAGACATCAT | 25909 |
rs115498568 | snp | A/G | 0.00636936 | 0.0560724 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838947 | CATTTACCTTACTAT[A/G]ATACTAAGTATCTCT | 25909 |
rs115531817 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888895 | GGCAACAGAGACCCT[C/G]TCTCTAAAAACAGAG | 25909 |
rs115533290 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878618 | ACTAAGAATGGTAAT[A/G]ATCAATCTGGCAGTT | 25909 |
rs115548322 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885846 | TTGGCTCTCAGTATC[C/T]ACAGGATCCATATCT | 25909 |
rs115550883 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916481 | TACATACAACTATAT[A/G]TTCATTACATAAAAC | 25909 |
rs115586890 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879498 | AAAATGGCTAAAGGT[C/T]GAAACAACCTAAATG | 25909 |
rs115677671 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890864 | ATAAGTGAGGTGGAA[A/G]AAAAGAAACCCAAAG | 25909 |
rs115712743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917702 | CTGGGAAGATGGCTA[C/T]GAAGCTTATATTCAG | 25909 |
rs115734630 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843358 | GGAATTTGCCTGAAT[C/T]ATTCTTGTGTAATTT | 25909 |
rs115790254 | snp | C/T | 0.112983 | 0.209108 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922236 | ATGGCAGTATGTGCC[C/T]GTAGTCCCAGCTACT | 25909 |
rs115821836 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897301 | TCTGGGCAACAGACC[A/G]AGATGCTGTCTCAAA | 25909 |
rs115893430 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911069 | TTTGTGCTATAAAGT[C/T]CAACTGCTTCCAATT | 25909 |
rs115894030 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882909 | AGGAAACTCAGGCTC[A/G]GAGAGGATAACTGAA | 25909 |
rs115894418 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855342 | AAAAAAATTCCATAT[A/G]TTTGTTAATTTCCCT | 25909 |
rs115896994 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920210 | AAAACACACAAGGAT[A/C]TCCAATAGCCAGCAG | 25909 |
rs115920770 | snp | C/T | 0.00359113 | 0.0422217 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891774 | TGATAAAACAAAGAG[C/T]GTACCTCTCTCAGTG | 25909 |
rs115955887 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901635 | ACAAAACAAAAAAAA[A/C]CAAAACACCCTGTCA | 25909 |
rs116023399 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912710 | ATTTCATTTTCTTTG[A/C]ATCTGAATAGAATTA | 25909 |
rs116044324 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841566 | ACTGTGTAACAAATA[A/C]ATCTGAAATGGAGTG | 25909 |
rs116084353 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868794 | CACGTGATGAATGAG[C/T]ACAGGTCTACCTCAT | 25909 |
rs116104791 | snp | C/G | 0.00450318 | 0.0472368 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890053 | CTTGACAACTGCACA[C/G]AATCATCTAGATTTT | 25909 |
rs116105455 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885396 | GACTGACTTTACTGA[C/T]TTAACGGCCAATTGT | 25909 |
rs116163292 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857969 | ACACTTTCTTCTTTT[C/T]TTTTTTTTGAGATGG | 25909 |
rs116210906 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918023 | GATACAAAACACATG[A/G]GATTTTTAATAAGGA | 25909 |
rs116252630 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883266 | ATGCAGCTTAACTTC[G/T]CGGACTTTTAGTTCA | 25909 |
rs116293629 | snp | A/G | 0.0205511 | 0.0992634 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838678 | GGACCAGGTCTTTGC[A/G]TGTTGTTCTGTCAAG | 25909 |
rs116306131 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920914 | AACATGGTGAATCCA[C/T]ATCTCTACTAATAAT | 25909 |
rs116315911 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897648 | GTAACACAATATGAA[G/T]TATACGTGTATTTAA | 25909 |
rs116412197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843566 | ACTGCTGGTAAAATA[C/T]GATCAGTAGCATACC | 25909 |
rs116430711 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910731 | TATCACACTGTCCTA[G/T]AACAGGGCCCCCACC | 25909 |
rs116432106 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919872 | CACAGAGCCAGGCAG[A/G]GTGGCTCATGCCTGT | 25909 |
rs116442883 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881276 | AAATTAAAACTCTTA[G/T]GTACCTAATATTCAA | 25909 |
rs116554934 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907063 | GTAACACAAACCTAG[A/G]TGAGATAGCCTACTA | 25909 |
rs116630006 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844395 | TTTGAACTACTTGTT[A/C]CAGCCAAAGGAACAG | 25909 |
rs116631711 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888055 | ATCCTGGGTTAACAC[A/C]TCTTCTTAAGAAAAC | 25909 |
rs116663150 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875817 | GCACACTTAGAAGTA[C/T]AGTGTAAACATTATG | 25909 |
rs116706274 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870458 | TAAAGATGTGATGAA[A/T]TGCTGTAATCTCATG | 25909 |
rs116721005 | snp | A/G | 0.0637235 | 0.166737 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840107 | CAAACCCTTTGATAA[A/G]GTTGCAAGTGAGCAG | 25909 |
rs116757531 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887622 | TTTTTATGAAGTCAG[C/T]AGCTCAGTAAATACA | 25909 |
rs116790263 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859487 | TGACTCACTGTTTGA[C/T]CTTCAACACCTAGAA | 25909 |
rs116829747 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914867 | GTGTCCATGTTTCCT[A/T]CTGTATGTGTTCTGA | 25909 |
rs116830294 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867989 | TTTTCTTTTAGACCA[A/G]TCTTGCTGTGTCACT | 25909 |
rs116831211 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922415 | TATCAACAGTATTCT[A/G]TTGCGGTTTTTTGGG | 25909 |
rs117071018 | snp | A/G | 0.00314033 | 0.0395007 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890064 | CACAGAATCATCTAG[A/G]TTTTTAAGAGTTGGA | 25909 |
rs117354341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913561 | TGTGATCTGAATAAT[A/G]AAATCTTCAGCTATA | 25909 |
rs117423076 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875159 | TGACATAGTAACTAA[G/T]TCTACACAACTGGGA | 25909 |
rs117448044 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851633 | TCTCATTCAGTCAAA[A/G]TAACTACATTTTGAG | 25909 |
rs117483369 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890483 | GCTTTGCAAGTTATA[C/T]TCTAAACAAATATAG | 25909 |
rs118117923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910432 | ACCAAAGAAGTGTTA[C/T]TGGCATTATGATTAT | 25909 |
rs118170973 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893070 | AACAGCTGAACTACC[A/C]AGTTAAACCCCCAAC | 25909 |
rs137861865 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854366 | GTTAGGAATCTACCC[A/G]AAAGAAATACTGACA | 25909 |
rs137866967 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926582 | AAATAGGGGCCAGGC[A/G]CGGTGGCTCACACCT | 25909 |
rs137895470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858955 | AATGTAGGCCAGGAC[C/T]GGTGGCGCATGCCTG | 25909 |
rs137993091 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881120 | CCACTGATTTCTAGT[A/G]ACTGGAGTAAAGTAA | 25909 |
rs138011766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859710 | TGTCCTGAGTAGCTA[A/G]GAATACAAGTGCATG | 25909 |
rs138016612 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928080 | CCCAAGGCAGGTGGA[C/T]CACGAGGTCAGGAGA | 25909 |
rs138056791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843298 | GTTTTCATCTCTTCA[A/G]TGAAACTGTGTATCT | 25909 |
rs138061071 | snp | C/T | 0.000480542 | 0.0154932 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851345 | GTATCAAAATTGTAC[C/T]GAAGCTTAAGTGTTC | 25909 |
rs138070764 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899281 | TACGTCTTCCGGCAG[C/G]CTGTCATTAGTAACT | 25909 |
rs138162884 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870316 | CAGTCTCAGCCACTC[A/G]GAAAGCTGAGGCAGG | 25909 |
rs138167920 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889734 | TTCCAGAAGTGTGGT[C/G]AAGACTCTCAACACC | 25909 |
rs138211146 | in-del | -/GAA | 0.079617 | 0.182947 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923079 | CAACCAAAGGAGAAT[-/GAA]GAAGAAGTTATTTAA | 25909 |
rs138217683 | snp | C/T | 0.0734246 | 0.176978 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931368 | TTATGTAACGAAGCC[C/T]GGCGCCCGCGAGCCT | 25909 |
rs138283580 | snp | C/T | 5.35585e-05 | 0.00517459 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876099 | TCAATGGCTAATTTT[C/T]GATGGACTCTAGGAA | 25909 |
rs138284466 | snp | C/T | 0.000525028 | 0.0161938 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849617 | GAAAGAAAAGTACCT[C/T]TTGCTTTCCTTGGAA | 25909 |
rs138324049 | snp | C/T | 0.000181382 | 0.00952145 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887273 | CTTGGCCCCAAGAAA[C/T]GGCAAATACAGTTGG | 25909 |
rs138354298 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868372 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 25909 |
rs138359914 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847307 | AAAAAAAAAACAAAC[-/A]AAAAAAAAAACTGAA | 25909 |
rs138371767 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899832 | AGTTCAAAATAAGTC[A/G]TAATTCCTTTATAAA | 25909 |
rs138430276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904246 | TCAACTAAATCGATG[C/T]TGTTTGCATACTGTA | 25909 |
rs138431892 | snp | C/T | 0.021333 | 0.101051 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862474 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 25909 |
rs138440333 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846967 | CACTAAGTTGCCCAG[C/G]CTGGTTGGATTTTGA | 25909 |
rs138503360 | snp | A/C | 0.403509 | 0.197319 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911610 | TGCCTCAGCCTCCTG[A/C]GTAGCTGGGATTAGA | 25909 |
rs138554302 | snp | C/T | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867679 | TTGAAAGGTGTGGTG[C/T]TATTTATAGGTTCTT | 25909 |
rs138568854 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890235 | TACAGAGGCACAAGT[C/G]AGAAAATGATCTGTC | 25909 |
rs138639898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904151 | CAAAACTAAAATCAC[G/T]GTGAAAAATTTAGTT | 25909 |
rs138652795 | snp | C/G | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855806 | CAACACTGGTACCTT[C/G]GACTTCTGGGTGAAG | 25909 |
rs138721438 | snp | C/T | 0.000115868 | 0.00761056 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876958 | ATCGTACCATAACAT[C/T]AATCTTCAGAGTTTG | 25909 |
rs138732353 | snp | A/G | 0.000680594 | 0.0184346 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902535 | CTAACCTTCATTCAC[A/G]CCTTCCTCCCTGTCA | 25909 |
rs138743895 | in-del | -/T | 0.0162968 | 0.0887851 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905528 | ACAAAACAAAGTTTG[-/T]TATGAGACCTACCTA | 25909 |
rs138747278 | snp | G/T | 0.00102165 | 0.0225784 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855764 | AATTGCAGGGGTGTA[G/T]GTTTCAACAGATGTT | 25909 |
rs138771252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926105 | ACTCTCATCATGTGA[A/G]TATCCTGCTCTCCCT | 25909 |
rs138777471 | snp | C/T | 9.2302e-05 | 0.00679283 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867399 | CACAAGGAGCACTGA[C/T]AACAAGTGGATGAGA | 25909 |
rs138782084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859372 | CTCTCCCATTTACTA[A/G]TGTTCCCCTGGCCCT | 25909 |
rs138785134 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928036 | AATTAAATACTGTTC[A/G]GCCGGGTGCGGTGGC | 25909 |
rs138811688 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866323 | AAAGGGGACTTGCAG[-/A]AAAAAAAAATCCGAA | 25909 |
rs138844491 | snp | C/G | 0.000154675 | 0.00879282 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850639 | TCTGACATCAGAATA[C/G]ATGTTTTCAGAAGCT | 25909 |
rs138879376 | snp | C/T | 0.00036318 | 0.0134706 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840899 | CACTTCTGTAGTTTT[C/T]CTTGGTTTGCTCTTG | 25909 |
rs138981192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900976 | AGGAATAGAGTAAGA[C/G]ACATCAACAGGAGAA | 25909 |
rs139002829 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932002 | GGGCGGAGAGGGAGG[A/G]GAGAACCGGCGGGAG | 25909 |
rs139003299 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869123 | TGCTGGATTACAGGC[A/G]TGAGCCACCACGCCC | 25909 |
rs139015537 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864888 | AAAAAAAAAAAAAAA[-/AA]GACTAGACTGACAAC | 25909 |
rs139036231 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871490 | AACCCTTTCAGAACT[C/G]TCAAGTTAACAAAGC | 25909 |
rs139055275 | snp | C/T | 6.65812e-05 | 0.00576942 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842732 | CGTCCTGATTCGTTT[C/T]GCTTTTGGCTTTCCC | 25909 |
rs139084142 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913522 | ATAGATTTAAGACTA[C/T]AGAGTAAATTTGCAT | 25909 |
rs139104475 | in-del | -/ACA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867903 | TACACCCCCCCCCCC[-/ACA]CACACACACACACAC | 25909 |
rs139118312 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869259 | CTAACTGTTCCCCCG[C/T]GTCTCTCCCTTTCCC | 25909 |
rs139187692 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896396 | AAAGGGGATGAAGTA[C/T]TGATACTTGCTATAA | 25909 |
rs139195625 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918663 | ACAGAGCAAAATCCA[G/T]TCTTAAAAACAAATG | 25909 |
rs139206093 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880791 | ATCCATTGCCAACAT[A/T]TAACAAATGTTTTAA | 25909 |
rs139209531 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897689 | GGTACAGTAAAAATA[C/T]ATTATTACAGGCTGG | 25909 |
rs139268547 | snp | C/T | 0.140919 | 0.224948 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927144 | GATCGTGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 25909 |
rs139301849 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883249 | TTGGGTGTTGGACTA[C/T]TATGCAGCTTAACTT | 25909 |
rs139374451 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928996 | TTAAGGAGTTTACAA[C/T]CTAGAAAAGGAGATA | 25909 |
rs139376112 | snp | A/G | 9.88745e-05 | 0.00703047 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902618 | TCGTCTGTCCCCTCA[A/G]AGGGAACATGCCACC | 25909 |
rs139377503 | snp | C/T | 0.000131872 | 0.00811902 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851105 | GCAATTTGTCCATGA[C/T]TATCATTTTCCCCAC | 25909 |
rs139497693 | in-del | -/ACACACACACACAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898652 | CACACACACACACAC[-/ACACACACACACAG]GAAAACTCCTGCAGT | 25909 |
rs139518980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906974 | ACACAGCCATGTGTC[A/G]CTTAACAAAAGGGGA | 25909 |
rs139521241 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932974 | AGTGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 25909 |
rs139538819 | snp | G/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839145 | TAAAGACATTTATAC[G/T]TAAGTACATACATTC | 25909 |
rs139612779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877978 | ACCGACAGGATTATC[C/T]TGAAGGTTCACTTGA | 25909 |
rs139625395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844897 | GTTTAACCAGTCTGC[C/T]GGAGTAAATCCCAGC | 25909 |
rs139627532 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920356 | AAAAATCAAGTAGAT[A/T]TGAAAAAATTTCTAA | 25909 |
rs139662726 | snp | C/T | 0.0414363 | 0.137845 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839395 | TCTTTATTCATTTAA[C/T]AAGTTCATTTAAATA | 25909 |
rs139666427 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901468 | TCTCTACTAAATATA[C/T]AAAAAATTAGCTGGG | 25909 |
rs139675122 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862907 | TAGCATGTAAATTTA[C/T]TTAGTAGAGATAATT | 25909 |
rs139678494 | snp | A/G | 0.000989935 | 0.0222258 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888373 | TAGACTCTAAATGAT[A/G]GCACATTACTGCAAA | 25909 |
rs139700015 | snp | C/T | 0.000248363 | 0.0111409 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877211 | CCATCAAGCCCATTT[C/T]CTGACAGACTTCATA | 25909 |
rs139736452 | snp | A/G | 0.000748509 | 0.0193312 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862039 | GAGGAGACCTTCCAG[A/G]TGATGGAGAGGGAGA | 25909 |
rs139833065 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858078 | CATTCTCCTGCCTCC[A/G]CCCCCCGAGTAGCTG | 25909 |
rs139851612 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892864 | TTGCTCAGGCTGGTC[G/T]TGAACTCCTGGCCTC | 25909 |
rs139868397 | snp | A/G | 0.0225638 | 0.103792 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864080 | CTCCGAACACTGAGA[A/G]GGCCGGGGGACAGGC | 25909 |
rs139900720 | snp | A/G | 1.77043e-05 | 0.0029752 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849585 | AGAGTGACTGAGATG[A/G]AAAACTGTTTTGCAG | 25909 |
rs139905601 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923440 | ATAAATACATAAATA[A/C]ATACATAAAATAATT | 25909 |
rs139947110 | snp | G/T | 9.90328e-05 | 0.00703609 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850247 | GATTTATCATCTTGC[G/T]TATTTCCTGTATTTT | 25909 |
rs140112899 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868481 | ACTGGTCTCAAACTC[C/T]GGGCCTCAAGTGATC | 25909 |
rs140125283 | in-del | -/TAAA | 0.0569829 | 0.158885 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867151 | ATTCATTTAATAATT[-/TAAA]AGTCTATAAAATGTT | 25909 |
rs140191724 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892096 | AAAAAGTGCTTTCAA[C/T]ATAAAACTAGCAAAA | 25909 |
rs140249572 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889626 | ATTCCCAGGTGATTC[A/G]GGTGTAAGAAACCTG | 25909 |
rs140249736 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933063 | ACCTCAGCCCTCCAA[A/G]TAGCTGGGACTATGG | 25909 |
rs140260985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869538 | TGTTAGTGGTTAATG[C/T]AGCTGATGACTTTAA | 25909 |
rs140268617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917147 | GGACAAGGAGAAGCA[C/T]AGAGTAGCCGCACTG | 25909 |
rs140283773 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894409 | AACCCCGTCTCTACT[A/G]AAAAATACAAAAAAA | 25909 |
rs140339459 | snp | A/T | 0.000329544 | 0.0128321 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851302 | AGTGTCTTTGTTATC[A/T]GCTAAGTCACAAAAC | 25909 |
rs140356512 | in-del | -/AT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846738 | TATATATACATATAC[-/AT]ATATATATTTTTTGG | 25909 |
rs140385845 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872498 | CTTACTCCAACCAAT[C/T]CAGAGTGACAACAGA | 25909 |
rs140397173 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903079 | AGAATCTGACAAAAG[G/T]CTATGAGACTTCGCC | 25909 |
rs140421518 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929988 | ACCTGGGAGACGGAG[A/G]TTGCAGTGAGCCAAG | 25909 |
rs140466849 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894677 | GTCTGTCAAATTCCT[C/T]TTTTGTGAGAACCAC | 25909 |
rs140505021 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870141 | AAAGAGCAAGAGAAC[C/T]AGAATGAGAAGCAGA | 25909 |
rs140585119 | snp | A/G | 6.59435e-05 | 0.00574172 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851147 | TTTTCTTCAGTTGCT[A/G]TGTTAGCTGCTTTAG | 25909 |
rs140597337 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841312 | CAAGGACGGGCCGAG[C/T]ACCAGTTGTCAGCCC | 25909 |
rs140602750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921437 | ACTTAATACTCAACA[A/G]AAACAAACTCAAAGG | 25909 |
rs140609930 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875932 | TCCAAGGCATGCCTG[C/T]ATGTGTTAGCGAAAG | 25909 |
rs140610300 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914773 | ATATTCTCTCTTCCA[C/T]ACACCAACCATGCAT | 25909 |
rs140613290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913795 | TTCAAGCCATAAAAT[C/G]ATTACGCATAAAACG | 25909 |
rs140742999 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927820 | CCATCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 25909 |
rs140774292 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885348 | ACACTGTATTTTCAA[C/T]CTGAATTTGATGCAG | 25909 |
rs140782802 | snp | C/T | 8.25144e-05 | 0.00642265 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889993 | TCAAACTTCTGTCGA[C/T]GACTGGTGTAGTAGT | 25909 |
rs140803492 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891337 | CTTTCACCTCAGCTA[C/T]ACTTTCATTTAGCTA | 25909 |
rs140831558 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898117 | CTACTTCACCTATTT[G/T]TGCAGAAATTATCTA | 25909 |
rs140851502 | snp | C/T | 0.000127137 | 0.00797199 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931084 | TGAGCTGGAACCTCA[C/T]GGCTGAGCCCCGAGT | 25909 |
rs140913748 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850300 | TCTCAATTTTCTGAT[C/T]ATTCTGCTAGGACTT | 25909 |
rs140999106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910135 | CATCTATAACCAGAG[A/C]TAATTTAATTTGCAG | 25909 |
rs141030289 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928681 | AAATACACAAATTCC[C/T]GCAGTAACTGAATTC | 25909 |
rs141067633 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860327 | TATTTCTCATAGCTA[C/T]TGGAAGGACTTTCAA | 25909 |
rs141076402 | in-del | -/TTG | 0.0588605 | 0.161139 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885341 | CCATGAACACTGTAT[-/TTG]TTTCAATCTGAATTT | 25909 |
rs141097043 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880302 | GGGTGTGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 25909 |
rs141147858 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858662 | GTGAAACCCCGCCTC[-/T]TAATAATACAAAAAT | 25909 |
rs141212789 | snp | C/T | 0.00755907 | 0.0610114 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838863 | TTGTTTCCCTTACTA[C/T]GATACTAAGTATCTT | 25909 |
rs141244743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870519 | TTACAGATAGGCAAA[C/T]AAGTGGTTTCTTGAG | 25909 |
rs141246553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880994 | AGACAGACTGAAAAC[C/G]CATCCTGTGGCAAAC | 25909 |
rs141282276 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895501 | GAGTAAAAAAGGTAA[C/T]CCAAAAAGGTTACAT | 25909 |
rs141292322 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875024 | TTGTTAAAACCATCT[C/T]CTGACAGGCCAACAA | 25909 |
rs141296664 | snp | C/G/T | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882286 | ACAGGCATGAGCCAC[C/G/T]GCACCTGGCCTATTA | 25909 |
rs141361259 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844135 | TAAGCCAAATGTGTA[A/G]GACGATTGAATGCTT | 25909 |
rs141409693 | snp | A/C | 0.00218216 | 0.0329609 | splice-donor-variant | AHCTF1 | GRCh38.p7 | 1:246867243 | TTTAATAAACTCTTA[A/C]CTAGAAATTTTTTGT | 25909 |
rs141440710 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914955 | ATTTACCTGAATGGC[A/C]ATAGTCTACTTGTTT | 25909 |
rs141450027 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861188 | CTTTTCAGGGCTGTT[A/C]AGGAAAAAAGATGTG | 25909 |
rs141575447 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865760 | ATAGTTTAAAGGTTC[-/AA]TGAGAAATCTTTTTA | 25909 |
rs141588111 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904932 | TCTCCAAGTATATTT[C/G]AAGAATAAGAGAGCA | 25909 |
rs141660666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899667 | TATTTTCATCCTAAG[A/T]ATAGATAACAAACCT | 25909 |
rs141670552 | in-del | -/TATG | 0.400147 | 0.19989 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884656 | CTTTCTCACAGTTAC[-/TATG]TGAGACTGTAATAAT | 25909 |
rs141689938 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872246 | AATTTGTACAAAATA[A/G]TACTCAGATCGGGCT | 25909 |
rs141764038 | snp | A/C/T | 0.150992 | 0.238404 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922961 | GCACTCTAGCCTGGG[A/C/T]GACAGAGCGAGACTC | 25909 |
rs141791876 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926909 | CCGGGCCGCGGTGGC[A/T]CACGCCTGTAATCCC | 25909 |
rs141831225 | snp | A/G | 0.000347553 | 0.0131778 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894703 | ACCACTTTATTCCAC[A/G]TCCATTCAAGAACAA | 25909 |
rs141845154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888867 | TATACACATGCCACT[A/G]CACTGCAGCCTGGGC | 25909 |
rs141851014 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846121 | ATGGCCTTAGGTATA[C/T]AGCAGGCCCTTCTTA | 25909 |
rs141857631 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899853 | CCTTTATAAAACATA[C/T]AAATACTAAATATCT | 25909 |
rs141859428 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852598 | AAGGATGCATGGGGC[A/G]GGGGTGTCAATCCTG | 25909 |
rs141864056 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928533 | GTTAAACAATAAAAT[C/T]AATTTTTTAAAACTC | 25909 |
rs141866586 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886440 | ATTGTATTAGATGTT[A/G]TAAGTAATCTACAGA | 25909 |
rs141990857 | snp | C/T | 0.000274661 | 0.0117156 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876171 | GATCTCTCCCGCAAA[C/T]GAGGATCACGATCAT | 25909 |
rs142087876 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902766 | TTTAAAGATTGTTCA[C/T]ACAATACAAAGAAAA | 25909 |
rs142129636 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898253 | AAATCTTGGGGAAAG[A/G]AGGCCAGCTACAAGA | 25909 |
rs142153444 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873550 | AAAGAATCCGTCCCA[A/G]TAATAAATATACTAG | 25909 |
rs142177309 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869128 | GATTACAGGCGTGAG[C/G]CACCACGCCCGGCCG | 25909 |
rs142193362 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862022 | AGTTTCTTTAAGTCG[C/T]TGAGGAGACCTTCCA | 25909 |
rs142196581 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903551 | ATCGCTTTTCACAGC[C/T]AGGTGCGGTGGCTCA | 25909 |
rs142240582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871514 | ACAAAGCCTTTCTTC[A/G]TAAATCAGAGTAACA | 25909 |
rs142265630 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920823 | AGGCACGGTGCCTCA[C/T]GCCTATAATCCCAGC | 25909 |
rs142290498 | in-del | -/AG | 0.365646 | 0.221644 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862717 | AAAAAAGTGCCAATT[-/AG]AGTAAGATAAATTAC | 25909 |
rs142302349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857869 | ATTTAGTGATTACTG[A/G]TAGTCTTGCATTATT | 25909 |
rs142338484 | snp | A/G/T | 0.000774708 | 0.0196682 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864019 | TTGAGGGCAGTGAAC[A/G/T]GGATACTAGGTACAA | 25909 |
rs142432026 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860343 | TGGAAGGACTTTCAA[C/G]TCAGACTATGGCATC | 25909 |
rs142569004 | snp | C/T | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850082 | ATTTTTCTTGGTCTA[C/T]CACGTTTTCTAGGTA | 25909 |
rs142571678 | snp | A/C | 1.65685e-05 | 0.00287819 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850038 | TCTCTTCCTTAACAG[A/C]CTTAGATCCTACATC | 25909 |
rs142573086 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925699 | CCCAGTGTTGGAGGT[A/G]GGGCCTGGTAGGAGG | 25909 |
rs142603415 | snp | C/T | 0.0066286 | 0.0571871 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850241 | TCACTGGATTTATCA[C/T]CTTGCTTATTTCCTG | 25909 |
rs142605416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887067 | TCTAAAATAGTGCTT[A/G]GTAAAGGTACTGATT | 25909 |
rs142609455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914664 | AAGACAAAAATAAAC[A/G]TAATGAGTGTATACT | 25909 |
rs142617351 | snp | C/T | 0.000511775 | 0.0159883 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889975 | CTATACCTTGATAAA[C/T]GCTCAAACTTCTGTC | 25909 |
rs142622327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858420 | AAAACTGAAGCCTAA[A/G]GTTATACTGCGTATC | 25909 |
rs142641335 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869936 | TCCTCTGAGAGATCC[A/G]AACAAAGTCCTTTGA | 25909 |
rs142641898 | snp | C/T | 4.95642e-05 | 0.00497792 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849900 | CCATCGAAAGTTCCT[C/T]GTTTGGCACTAAAAT | 25909 |
rs142646495 | snp | C/T | 6.66322e-05 | 0.00577163 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900406 | AAATATACAGAAGGC[C/T]TTCCCTGTCCATATA | 25909 |
rs142686289 | snp | A/G | 0.00236533 | 0.0343085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918384 | ATACTTCCACTGTAA[A/G]TATTTTTAAAAGAAA | 25909 |
rs142720037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872644 | AAAACATAAGGATCA[C/T]GCTAGCCAAACTATG | 25909 |
rs142727111 | snp | A/C/G | 0.000645246 | 0.0179503 | synonymous-codon, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876959 | TCGTACCATAACATT[A/C/G]ATCTTCAGAGTTTGG | 25909 |
rs142808731 | in-del | -/TA | 0.0383715 | 0.133092 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880225 | CAATATGTTATTTGT[-/TA]TATATATATATAAAA | 25909 |
rs142939758 | in-del | -/AACCCCC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896134 | GAATGTAAAATGGAA[-/AACCCCC]CAGCCACTCTGCAAA | 25909 |
rs142949133 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932736 | ACCGCGGGTTTTCAT[C/T]GTGGAATTTCTTATT | 25909 |
rs142973217 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932102 | AAACTCTCGGTGAAA[A/G]AAGGAGGTGGGAGGG | 25909 |
rs143001336 | snp | C/T | 2.08488e-05 | 0.00322861 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905685 | AGTATATTTCATATT[C/T]TTAAGTTATTTTTTA | 25909 |
rs143015692 | snp | A/G | 0.239037 | 0.24976 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868413 | GGCGTGAGCCACTGC[A/G]CCTGGCAATTTTTGT | 25909 |
rs143015709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911961 | TTCTTTGAGATGGAT[A/T]CTTGCTCTGTCGCCC | 25909 |
rs143057343 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896715 | ATCTGAACTGCACGG[A/T]GTATGAAATATCTCA | 25909 |
rs143060611 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889528 | AAGCTAATGTTCACT[A/C]TCCTAAATTGGTCAT | 25909 |
rs143078740 | snp | C/T | 0.030665 | 0.119967 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869100 | CCGCCCGCCTTGGCC[C/T]CCCAAAGTGCTGGAT | 25909 |
rs143171849 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895261 | TTGATTTTTTATGAT[C/T]ACAAAGTGGTTTTGT | 25909 |
rs143201658 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926901 | GTGTATGGCCGGGCC[A/G]CGGTGGCACACGCCT | 25909 |
rs143228130 | snp | A/G | 0.040671 | 0.13668 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845919 | GATATTTAACAATTG[A/G]CTCTTACCAGCCAGT | 25909 |
rs143229745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864286 | CAAAAAGTCAGAAAA[C/T]TATTCATCGCAAAAC | 25909 |
rs143234124 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932997 | CTGGAGTGCAGTGGT[A/G]TAATCAAGGCTCACA | 25909 |
rs143242697 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904702 | TAGTGAACTCAAGCA[C/T]GAAGCATGCAGTAAG | 25909 |
rs143245095 | snp | A/G | 0.00084855 | 0.0205805 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842733 | GTCCTGATTCGTTTC[A/G]CTTTTGGCTTTCCCA | 25909 |
rs143290948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868671 | TGGACATGTGCCTTC[A/C]ACTGAAATAGGAGTT | 25909 |
rs143303729 | snp | C/T | 0.00459057 | 0.0476887 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850190 | CTAACTTCTCTCCCT[C/T]TGACCCTTCTAACAT | 25909 |
rs143330344 | snp | C/T | 0.000837535 | 0.0204467 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853205 | TTCTTTTAAGTTCAG[C/T]GCTACTTCCTGGTTA | 25909 |
rs143336719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876314 | CCTACATATCCATTT[C/T]TCCAAACCAAGAACT | 25909 |
rs143342715 | in-del | -/AAGATCGCTTAAGCCCAAGAGGTTGAGGCTACAGTGAGCCATGAC | 0.410399 | 0.191761 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897888 | GGGGGCTGGGGTGGG[lengthTooLong]CATGCCACTGCATTC | 25909 |
rs143355150 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923658 | CAAAGACATTACACA[C/T]GGCTAGAGTGAAGTG | 25909 |
rs143410016 | in-del | -/TC/TCTG/TCTTC/TTCT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857965 | CTAACACTTTCTTCT[-/TC/TCTG/TCTTC/TTCT]TTTTTTTTTTTTGAG | 25909 |
rs143458956 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913602 | CACCATTACTCAATA[C/T]ATAGAAAAATCACGC | 25909 |
rs143481519 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927602 | ACAGAATCCCAGCCT[C/T]TTATGACATGCCAGC | 25909 |
rs143519690 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843626 | CAAAGGGGTGGATAC[A/C/G]ACCATTTTTGGCTTT | 25909 |
rs143531926 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847081 | TATCTGAGGTCAGGC[A/G]TTTGAGACTAGCTTG | 25909 |
rs143544844 | snp | C/T | 9.89071e-05 | 0.00703163 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851135 | CTGCATACAAGTTTT[C/T]CTTCAGTTGCTGTGT | 25909 |
rs143551247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899248 | CATCTACATAAATTA[A/G]TTGCTAAAAACATAC | 25909 |
rs143584393 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861785 | GTTTGGCTTAGCCAA[C/T]GGCCCTAGTGTTTCT | 25909 |
rs143609888 | in-del | -/TTTA | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933122 | CATTAATTTTTTTAT[-/TTTA]TTTATTTATTTATTT | 25909 |
rs143648189 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879506 | TAAAGGTTGAAACAA[A/C]CTAAATGTTCATTAC | 25909 |
rs143650145 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879005 | ACCAAAATCTAGAAA[C/T]GTTAAAAGCAGAACA | 25909 |
rs143704658 | in-del | -/ACACACACACACACAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898622 | TGACATCTTGACAAA[-/ACACACACACACACAC]ACACACACACACACA | 25909 |
rs143718823 | snp | C/T | 0.00148542 | 0.0272122 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840884 | AAGACCTGTTCCTGT[C/T]ACTTCTGTAGTTTTT | 25909 |
rs143718915 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882666 | GCCTATACAAAAGGA[C/T]TTTTTGGCTTTCTTG | 25909 |
rs143797194 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895029 | AGGCCTAATTCCTTT[-/A]AAAAAAAAAAGGTCA | 25909 |
rs143813373 | snp | C/T | 0.00377385 | 0.0432745 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842717 | TTGTTTTGTTTTTGA[C/T]GTCCTGATTCGTTTC | 25909 |
rs143835885 | snp | A/T | 0.000846308 | 0.0205533 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850402 | TCTAGGAGTCCTTTT[A/T]GTAACAGATGAAACC | 25909 |
rs143868238 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860241 | CCACTGCACTCCAGC[C/T]TGGGCAACAGAGTGA | 25909 |
rs143876978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869523 | ACAGGGTGACTCTGC[C/T]GTTAGTGGTTAATGT | 25909 |
rs143883846 | snp | C/T | 0.00772473 | 0.061666 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891042 | GAAACCACAAACTTA[C/T]TGCTTAAGTCTATCA | 25909 |
rs143911818 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862645 | TTATACGTAAGTCTA[C/T]GAAACATAAAACTGC | 25909 |
rs143918265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867438 | CAGAGGGTTTTCATT[C/T]GTTTTACTTTGTACA | 25909 |
rs143922986 | snp | A/C | 0.000134969 | 0.00821378 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853246 | CAGAGACAATAGGAC[A/C]TTCAGAGATAGTGAG | 25909 |
rs143967117 | in-del | -/ACAC | 0.454311 | 0.144073 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898622 | TGACATCTTGACAAA[-/ACAC]ACACACACACACACA | 25909 |
rs143983840 | snp | A/G | 0.0558544 | 0.157504 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933204 | AGTGGCACAATCTCG[A/G]CTCACTGCAACCTCC | 25909 |
rs143991448 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920077 | GAACCCAGGAGGCAG[C/T]TGCAGTGAGCCGAGA | 25909 |
rs144046700 | snp | C/T | 0.000379328 | 0.0137666 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888210 | TTCAGTAACGCCGTC[C/T]AATAGGTACATATCA | 25909 |
rs144114580 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844837 | AACTATAGGGCCCCC[A/G]TATTAAAAGCAATTA | 25909 |
rs144204001 | snp | C/T | 0.367913 | 0.220446 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841911 | ATTCTGCCTCAGCCT[C/T]CAGAGTAGCTGGGAC | 25909 |
rs144251691 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845154 | TCAGCTACTGGGATA[A/G]TCAAGAGTTCTATCA | 25909 |
rs144301715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890395 | TGAAAAAATAAGATC[A/G]ACAATTATGTACAGT | 25909 |
rs144318625 | snp | A/C/T | 0.000395299 | 0.0140534 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849722 | CGAGTCCTGCTGCTG[A/C/T]GGGATGATTTAGTGA | 25909 |
rs144319690 | snp | A/T | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851085 | TTACGGCAGATGGCA[A/T]ATTTGCAATTTGTCC | 25909 |
rs144381131 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901572 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCAACTG | 25909 |
rs144439704 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922940 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCTAGC | 25909 |
rs144446615 | snp | C/T | 1.65037e-05 | 0.00287256 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863882 | CTTGAAAAGTAAGAG[C/T]CATCTAGTTTGATTG | 25909 |
rs144461673 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909707 | TTGATTTAATAAGGA[A/C]AAATCATAATGTGTG | 25909 |
rs144481579 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914242 | GTTTGGTGATTTCTA[C/T]GCTAATACAGGTTGA | 25909 |
rs144509730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868813 | GGTCTACCTCATTTT[A/G]TTGTGCTTTGCTTCA | 25909 |
rs144544553 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857437 | TGTGAGCGAAATCTT[C/G]GTCTTCAACAAAAAC | 25909 |
rs144597398 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859083 | CTCAAATAAGTAAGG[C/T]AGTGTAAATTTCTAG | 25909 |
rs144599339 | snp | A/G | 0.00881315 | 0.0657944 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888412 | CAGACTAGCAGGAGG[A/G]TATTTTCCTGTGCCT | 25909 |
rs144607057 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929274 | ATTAGCCGAGTGTGG[C/T]GGCGCGTTCCTGTAG | 25909 |
rs144631810 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861497 | TTCCCTAATTGGTAA[C/T]ATACCAGTATTTTCA | 25909 |
rs144747230 | snp | A/G | 0.0088679 | 0.0659948 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850762 | TGATTTGACATTCAC[A/G]TTTTGGATACGTTGA | 25909 |
rs144855018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863537 | AGTAACAGTTTTGTC[A/G]AAGAATTTAAATAAA | 25909 |
rs144863253 | in-del | -/GGGCG | 0.361684 | 0.223667 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838605 | GCAAGTTGTAGAAGT[-/GGGCG]GGGCGGGGCGGGGGG | 25909 |
rs144894125 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884371 | TTACCCTCTTATCCG[C/T]AGAAGTACATGCTAT | 25909 |
rs144969316 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870556 | TCTACAGTGTTGAAA[C/T]GATAAAGTGTAAACA | 25909 |
rs144970789 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929131 | AGAGTACAGTGGGCT[C/G]GGTGCGGTGGTTCAC | 25909 |
rs144971133 | in-del | -/TA | 0.00795532 | 0.062565 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838826 | TGTTTCCCTTACTAC[-/TA]TGATACTAAGTATCT | 25909 |
rs144994178 | snp | C/T | 0.000296721 | 0.0121767 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861050 | CTCTTCAAGGTCTTC[C/T]GGTGACGGTGCATCC | 25909 |
rs145003209 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908840 | GAGGCAGAGCTTGCC[A/G]TGAGCCAAGATTGAG | 25909 |
rs145065480 | snp | A/C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839223 | TATGATCTACATTCA[A/C/T]GGAGGGGGGAAAAAA | 25909 |
rs145090622 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879086 | TCACAACAAGGTTGA[-/T]TTTCCCTAATGCATA | 25909 |
rs145112684 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912200 | AATCAAGAATGTGCC[A/G]GGTGTGGTGGCTCAC | 25909 |
rs145124901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866356 | ATTGGTAGAAAAAAA[C/G]AATGTCGGTAATAAC | 25909 |
rs145140945 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933924 | GGAGGTTTGGGGTTC[A/G]TTGTCTTAATTATTT | 25909 |
rs145146408 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915187 | ATACAAAAATTAGCT[C/G]GGCGTGGTGGTGCAC | 25909 |
rs145149158 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883539 | GCCTTTTGCAAAATT[A/T]TCAGTTCAAAAATTT | 25909 |
rs145203002 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845512 | CAAAAGTATTTCTAC[A/G]AAAATTATACATTCT | 25909 |
rs145223994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889712 | GCAACTCGAGGAAGA[C/T]GACTATTTCCAGAAG | 25909 |
rs145295081 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889333 | CACTTACTACTCTTT[C/G]CGGTTGTCCAATGAG | 25909 |
rs145462531 | snp | C/T | 1.65479e-05 | 0.0028764 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849959 | TCAACATTTTCACTT[C/T]TAGCTGGGGTATTTC | 25909 |
rs145510203 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905607 | TTCTCAGGTTCTTGA[A/G]AAGTGACAGCATATA | 25909 |
rs145530946 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894383 | CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 25909 |
rs145531202 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930016 | AAGATTGTGCCACTG[A/C]ACTCCAGCCTGGGCA | 25909 |
rs145568373 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840069 | AATATCCATAAACAG[A/G]TTTATTTTACATTTC | 25909 |
rs145576635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914243 | TTTGGTGATTTCTAC[A/G]CTAATACAGGTTGAA | 25909 |
rs145601846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889313 | CTAATTGTGAATAGC[A/G]GCAGCACTTACTACT | 25909 |
rs145616559 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852996 | TTATATAGCAGTCAA[A/C]TAAATGAACGTGTTA | 25909 |
rs145616761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892233 | TCAATATTTAATGTG[C/T]CACTGGTCTAGAAAA | 25909 |
rs145634607 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910716 | AAGGGGGAAAAATCA[C/T]ATCACACTGTCCTAG | 25909 |
rs145641591 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914846 | CCTCATCCAAATGAT[A/C/G]AATGAGTGTCCATGT | 25909 |
rs145649060 | in-del | -/AA | 0.0944967 | 0.195752 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924010 | GAATATAAATCTGGC[-/AA]AAAGAGAGATCCGAG | 25909 |
rs145670190 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899098 | CCGTCTCAAAAAGAG[A/G]AAAGTATTTTTCAAA | 25909 |
rs145680709 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924845 | TTATCCAAAACAGAT[C/T]CAAAAGTCTAACCTA | 25909 |
rs145681656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858315 | CCCCCTTAACCTCTC[A/G]CTTTTCACTTTTTGC | 25909 |
rs145708659 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852194 | AAATAACCTAGAAAT[C/T]AGGATTCCCACTTAC | 25909 |
rs145750705 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910544 | CACATATAGCAAATG[C/T]TGAAAATTAACTTGA | 25909 |
rs145867818 | in-del | -/CT | 0.0205511 | 0.0992634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925062 | CTATGTTGTTTTCCC[-/CT]CTGACAGCCTTTTAT | 25909 |
rs145980470 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901845 | AAATAAATAAACAAA[C/T]AAAAACTTTAAAAAG | 25909 |
rs145999407 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887114 | CAACTATTTTTAGTA[G/T]ACTGTATCATATCTT | 25909 |
rs146002900 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849516 | TTTGAGGGGGGAAGG[G/T]GAAAAATTCCCTATA | 25909 |
rs146052498 | snp | C/T | 0.000501866 | 0.0158329 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867245 | TAATAAACTCTTACC[C/T]AGAAATTTTTTGTGA | 25909 |
rs146102598 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924084 | TGAGTACAGAAAGGA[C/T]TACATTCAGTTCCAA | 25909 |
rs146126599 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868466 | CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC | 25909 |
rs146143857 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869121 | AGTGCTGGATTACAG[A/G]CGTGAGCCACCACGC | 25909 |
rs146242458 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926985 | CGAGACCATCCTGGC[C/T]AACAAGGTGAAATCC | 25909 |
rs146245760 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882543 | CTATGTGGGACATTC[A/G]ATATATACTTTTGTA | 25909 |
rs146246798 | snp | C/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902616 | ACTCGTCTGTCCCCT[C/G]AAAGGGAACATGCCA | 25909 |
rs146264026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886623 | TTCTGATCTACAGTT[C/G]ATTGAAGCCACGGAT | 25909 |
rs146287436 | snp | A/G | 8.23974e-05 | 0.00641809 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895908 | TGCTGCTGACAATAT[A/G]GCTTCTAACTGTTCT | 25909 |
rs146398045 | in-del | -/GGTACAGTGGGGTCTGAGAACGCCAA | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917434 | TTAAGAAAGTAGCAT[-/GGTACAGTGGGGTCTGAGAACGCCAA]GGTTCCAAGATCCTT | 25909 |
rs146417813 | snp | C/T | 0.00499005 | 0.0497003 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843811 | AGTTCATCTTCAAGC[C/T]TGTTCTTATTGGATG | 25909 |
rs146464504 | snp | A/G | 0.00253883 | 0.0355383 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861203 | CAGGAAAAAAGATGT[A/G]GTCCTATCTTTGCTC | 25909 |