SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs371585680 | in-del | -/CACT | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811497 | ACACACACTCTCTCT[-/CACT]TACTCACATGTTTCT | 405 |
rs371695142 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150856193 | TGCCTGTAATCCCGC[A/T]CTTCGGGAGGCCAAG | 405 |
rs371745420 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875300 | AAATGACGTGACAAA[C/T]TAACCATTTCTTAAA | 405 |
rs371766354 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150840044 | CCAGGAGTTTGAGAC[C/T]GGCCTGGCCAACATG | 405 |
rs371836293 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150814545 | ATAACAGTAAAGTAT[C/T]ATATGCAGGCCAGGC | 405 |
rs371836643 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859213 | CTAAATTCCAATACT[G/T]AAAAGAAAATTATGT | 405 |
rs371861989 | snp | A/G | 2.06729e-05 | 0.00321497 | intron-variant | ARNT | GRCh38.p7 | 1:150836506 | TTCCTGCGCAAGAAA[A/G]AGAAATAGAAGTTAA | 405 |
rs371939589 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851569 | TTACCCCCAACCCAG[C/T]GCTCTCTGAAACATG | 405 |
rs371953713 | snp | A/C | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877262 | AGCGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAG | 405 |
rs371971592 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866240 | CACCTGCCTCAGCCT[C/T]CCAAAATGCTGGGAT | 405 |
rs371989593 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867541 | AAAGAAAAAGAGAGA[G/T]ATATCTTTTAAATAG | 405 |
rs372256938 | snp | C/G | 0.000280077 | 0.0118305 | intron-variant | ARNT | GRCh38.p7 | 1:150817336 | AATACTCCCTACCCT[C/G]TTCAACGAAGAGGAC | 405 |
rs372272870 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845816 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 405 |
rs372358680 | snp | C/T | 4.94947e-05 | 0.00497443 | intron-variant | ARNT | GRCh38.p7 | 1:150839419 | GATTCCAGACTCTCT[C/T]AGAACTATAAGTCCC | 405 |
rs372372527 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849169 | GATCATACCATTGCA[C/T]TCCAGCCTGGGCAAC | 405 |
rs372391759 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150829433 | CCATACATTTACACT[G/T]TACCAAGTTAGTAAA | 405 |
rs372477776 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150830850 | TGCTACATAGAGGTA[C/T]GAAAGATCACATACT | 405 |
rs372603018 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150851302 | CGCCTCTGCCCGGCC[A/G]CCCCTTCTGGGAAGT | 405 |
rs372659212 | snp | C/G | 0.000104782 | 0.00723739 | intron-variant | ARNT | GRCh38.p7 | 1:150812132 | AAAGAAAAAGATTAA[C/G]TTTGGGTCACACACC | 405 |
rs372741267 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816630 | ACAGGTGCAAAGAAA[C/T]AGGAGGAAGAAAAGC | 405 |
rs372769481 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150855297 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 405 |
rs372833219 | snp | C/T | 3.30387e-05 | 0.00406427 | synonymous-codon | ARNT | GRCh38.p7 | 1:150831846 | GGCCTTGATGTAGCC[C/T]GTGCAGTGGACCACC | 405 |
rs372837223 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813647 | TAGTTTTTTTTTTTT[A/T]TTTTTTATTTTTTTG | 405 |
rs372906962 | snp | C/T | | | utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150876570 | TAGTCGCCGCCATGG[C/T]CGCAGATGCCACCGC | 405 |
rs372919836 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857071 | AAACCGTAAGTCACC[C/T]ATAATACTATTACCC | 405 |
rs372944017 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150836625 | GTTCACACCTGATCC[A/C]CAGCCACAGGTTTCC | 405 |
rs372950126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150823705 | ACAGGCGCGTGCCAC[C/T]ACGCCCAGCTAATTT | 405 |
rs372979233 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150825678 | ACGTGGTGAAACCCC[A/G]CCTCTACTAAAAATA | 405 |
rs373016604 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | ARNT | GRCh38.p7 | 1:150839485 | AGCCATCAGTGGATG[C/T]GTTGCCAGTTCCCCG | 405 |
rs373043653 | in-del | -/T | 0.449979 | 0.150028 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858616 | GATTGCTCTTCTTGA[-/T]TTTTTTTTTTTTTTT | 405 |
rs373091438 | snp | C/T | 0.000100241 | 0.00707886 | intron-variant | ARNT | GRCh38.p7 | 1:150842485 | TAAAAATAGAATTAA[C/T]GAACTAAGCTAAAAT | 405 |
rs373223362 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873053 | ACTTTGGGAGGCCGA[A/G]GCAGGCGGATCACAA | 405 |
rs373299337 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868950 | CCTGGGCAACATAGC[A/G]AGATCCTGTCTCTAC | 405 |
rs373341799 | in-del | -/AG | 0.00636936 | 0.0560724 | intron-variant | ARNT | GRCh38.p7 | 1:150869569 | TTTTTTCCTAGAGAC[-/AG]GGGCTCACTCTGTCA | 405 |
rs373354853 | snp | C/T | 0.00120168 | 0.0244826 | intron-variant | ARNT | GRCh38.p7 | 1:150860433 | GTTGGCCAGGCTGGT[C/T]TTTAACTCCTGACCT | 405 |
rs373462932 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852374 | AAAAAACACATAGAC[A/G]GAAATACCCAGCCAT | 405 |
rs373498149 | in-del | -/G | | | frameshift-variant | ARNT | GRCh38.p7 | 1:150813208 | GGTTGCTGTGCTGGC[-/G]GGTTGTTGAACATGT | 405 |
rs373530200 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150834889 | GGAAAAGTAGGAGTG[A/G]AAAGTAGTAGTAGAA | 405 |
rs373541902 | snp | C/T | 2.50881e-05 | 0.00354167 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858369 | TCGCCGCTTAATAGC[C/T]CTCTGGACAATGGCT | 405 |
rs373593957 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835594 | CAAGAGAGAGACCCT[A/G]TCTCTTTTTTGGGTG | 405 |
rs373648605 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150826874 | CTGGTCTCGAACTCC[C/T]GACCTCAAGTGATCC | 405 |
rs373689676 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150851010 | GCCCCTCTGCCCGGC[A/C]GCCACCCCGTCTGAG | 405 |
rs373782271 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150840343 | TATAACCTCAGCTTG[G/T]TTAACTCCCATGCTT | 405 |
rs373807042 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150870995 | AATATAGTGAGACCC[A/G]GTCACTATCTAAAAT | 405 |
rs373865234 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150814311 | ACCATGCCTATGAGA[-/T]GTCAACACTGTCAAT | 405 |
rs373867153 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819106 | ACTAGGTATTATTCA[C/T]ATTTGCTAAGTAGTC | 405 |
rs373894722 | snp | A/G | 6.59337e-05 | 0.0057413 | intron-variant | ARNT | GRCh38.p7 | 1:150832438 | AAAAGCAATCAGACT[A/G]CCCTATCAAAGAACT | 405 |
rs374049564 | in-del | -/AAAACAA | | | intron-variant | ARNT | GRCh38.p7 | 1:150840260 | AAAAACAAAAAACAA[-/AAAACAA]GAGAAAAAAAAAGAT | 405 |
rs374061602 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150873149 | AAAAAATTAGCCGGG[C/T]GTGGTGGCGGGTACC | 405 |
rs374070096 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861522 | TAACGGATAAAGAAA[C/T]TGTGGGGCTGAACAT | 405 |
rs374080706 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870096 | GACTGTGTAGATGGA[C/T]TGCCAACAATAAAAT | 405 |
rs374089243 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | ARNT | GRCh38.p7 | 1:150816320 | GCTCCTTGGGTGGGG[C/T]TGGAGTGGCGGGAAA | 405 |
rs374110573 | snp | C/G/T | 5.21574e-05 | 0.00510651 | intron-variant | ARNT | GRCh38.p7 | 1:150813374 | AATAAACAACTCCAA[C/G/T]CTACACAATTCCATT | 405 |
rs374113061 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150840649 | AGTCCCATATGGGTC[A/C]CCAGTCTGGGACGAA | 405 |
rs374215917 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854631 | GGAAGCTGAGGCAGG[C/G]GGATCACTTGAGGTC | 405 |
rs374226509 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150813381 | AACTCCAATCTACAC[A/G]ATTCCATTGTGTACT | 405 |
rs374246188 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150832006 | ATGCTCTTAGGAGTT[C/T]AGAAAACAGGATAAT | 405 |
rs374267433 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861165 | ACTGCTAGTGGAAAT[C/G]TAAAATGGCGTAACA | 405 |
rs374268272 | in-del | -/AAAAA | | | intron-variant | ARNT | GRCh38.p7 | 1:150832035 | TCATCTTTCCCACCC[-/AAAAA]AAAAATGACCGCCAC | 405 |
rs374278306 | snp | C/T | 1.66344e-05 | 0.0028839 | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150842444 | AAGTCTCTCTTTATC[C/T]GCAGAGCTCTGCTCA | 405 |
rs374281866 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856747 | CAGCCTGGCAAAAGA[A/G]CAAGACTCTGCCTCG | 405 |
rs374287701 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838028 | ACCAAAACTAATTAA[A/G]TAGTCGCCCTGCTTT | 405 |
rs374307636 | snp | C/T | 1.73075e-05 | 0.00294167 | intron-variant | ARNT | GRCh38.p7 | 1:150816443 | AAAAGATTAAAAGGA[C/T]AGATTTATCACAGAA | 405 |
rs374319779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864528 | CAAAAAACCAAACAC[C/T]GCATATTCTCACTCA | 405 |
rs374453267 | snp | C/G | 1.65075e-05 | 0.00287289 | intron-variant | ARNT | GRCh38.p7 | 1:150834508 | TTGATCCTTCCTATA[C/G]CAAATCACAATCCTC | 405 |
rs374455395 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150862713 | AGATCCTGCCTCTGT[A/T]AAAAAAAAAAAAAAA | 405 |
rs374457477 | snp | A/G | 0.000875616 | 0.0209055 | intron-variant | ARNT | GRCh38.p7 | 1:150842360 | AAGAAAAGAAAGAGT[A/G]AGAAAAAGGATAGAA | 405 |
rs374462806 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871821 | GCTGAGGCGGGAGAA[C/T]AGCTTGAACCCAGGA | 405 |
rs374493943 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810662 | AAAAGCTGGTATCTA[C/T]GACTGTTACCTGAGG | 405 |
rs374503314 | snp | G/T | 0.000227744 | 0.0106686 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858303 | ATTCAGCAACTAAAG[G/T]TGGTTTATAGGAGAG | 405 |
rs374552527 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150850334 | CCTCTGATGCCGAGC[C/T]GAAGCTGGACTGTAC | 405 |
rs374597261 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838365 | ATTTATTTATTTACA[A/T]GTCTGTTTCCACCAG | 405 |
rs374603369 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | ARNT | GRCh38.p7 | 1:150850788 | CGGCTGCCCAGTCTG[C/G]GAACTGAGGAGCGCC | 405 |
rs374650042 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815441 | GTAGTCCCAGCTACT[C/G/T]GGGAGGCTGAGGCAG | 405 |
rs374674319 | snp | C/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878607 | AATTTACATATTATT[C/G]TTTACATCTGTTAAA | 405 |
rs374728595 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867948 | CTCCCATACAGCCTG[C/T]GGAACTATGAGTCAA | 405 |
rs374739091 | snp | A/T | 1.72847e-05 | 0.00293974 | intron-variant | ARNT | GRCh38.p7 | 1:150830021 | TTAACGGGGACCTCC[A/T]ACTCAAATGCCTTCA | 405 |
rs374773764 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873058 | GGGAGGCCGAGGCAG[A/G]CGGATCACAAGGTCA | 405 |
rs374797441 | snp | C/T | 0.00592201 | 0.0540919 | intron-variant | ARNT | GRCh38.p7 | 1:150861242 | CTGGGTGCAGTGGTG[C/T]GCACCTGTAGTCCCA | 405 |
rs374847969 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150824180 | TTGGTGCAAAAGTAA[C/T]TGCATTTTTTGCCAT | 405 |
rs374906557 | snp | C/T | 3.33039e-05 | 0.00408055 | intron-variant | ARNT | GRCh38.p7 | 1:150826624 | CTTGGCTCACTGCA[C/T] | 405 |
rs374968833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150856207 | CACTTCGGGAGGCCA[A/G]GGCGGGTGGATCACG | 405 |
rs375029621 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875431 | AAAAAAAATCTAATT[C/T]AAATTTCAACGTGGG | 405 |
rs375084790 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827026 | TCTTCTGTTTTAATC[C/T]TAAGATTATAGTTAA | 405 |
rs375114362 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150824677 | TAGGCTGGTCTCAAA[-/A]CTCCTGACCTCAAAT | 405 |
rs375140640 | snp | C/T | 0.000428477 | 0.0146306 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817179 | GCTGTGTTCTGGTCC[C/T]GTGGTTGTCACAGGC | 405 |
rs375165387 | snp | A/G | 8.24232e-05 | 0.0064191 | intron-variant | ARNT | GRCh38.p7 | 1:150839426 | GACTCTCTCAGAACT[A/G]TAAGTCCCAGAGACC | 405 |
rs375175118 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | ARNT | GRCh38.p7 | 1:150834680 | CTGGAGTGCATTTTT[A/G]TGTGTGGGGAAGAGG | 405 |
rs375243843 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150866751 | AAGAGTTAATAACCC[A/G]GATAAACACATAAAA | 405 |
rs375273213 | snp | C/T | 0.000189233 | 0.00972525 | intron-variant | ARNT | GRCh38.p7 | 1:150829503 | GCTATGCTGAACTCA[C/T]TACTCAGGTTGATAT | 405 |
rs375304467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855549 | CCTGGACAACAAAGC[A/G]AGACTCCGTCTCAAA | 405 |
rs375416807 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150842117 | AAGCACCAACTGGCA[C/T]GGTTGCATTCCTTCT | 405 |
rs375439313 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840945 | CTTATCTCTCTTCTT[C/T]TTTTTTTTTTTTTTT | 405 |
rs375520364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857135 | TATGTACATGTTATA[C/T]ATATCTTTTGACAGT | 405 |
rs375531114 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865109 | GATTAATAAAAAAAA[C/T]AAGGTGATAAAGGCC | 405 |
rs375531372 | snp | A/G | 0.000116001 | 0.00761491 | missense | ARNT | GRCh38.p7 | 1:150836441 | CTGCCTGTCTCACAT[A/G]AGACAATAAACAGAA | 405 |
rs375595969 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARNT | GRCh38.p7 | 1:150825774 | GAATCGCTTGAACCT[A/G]AGAGGCAGAGGTTAC | 405 |
rs375597772 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852564 | GGGTTTGTAAATGCC[A/G]TCCTCTCCTCACTGA | 405 |
rs375608178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857988 | ATTCTAGAGCTCAGC[A/T]TTCTCTAAATTCAGA | 405 |
rs375654626 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825621 | CTTGGGAGGCTGAGG[C/T]GGGTGGATCACGAGG | 405 |
rs375672804 | snp | G/T | 1.64939e-05 | 0.0028717 | intron-variant | ARNT | GRCh38.p7 | 1:150816908 | GTGGACCAAAAGGAG[G/T]TGGGGAAGGGCCAGT | 405 |
rs375675621 | in-del | -/TCAG | | | intron-variant | ARNT | GRCh38.p7 | 1:150866281 | AGCCACCAAGGTCAG[-/TCAG]CCTGTTCCAAGGTCT | 405 |
rs375732355 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825325 | TTATATTCATTACCT[C/T]ATTTAATCTTCCCAA | 405 |
rs375752258 | snp | C/T | 1.64879e-05 | 0.00287118 | synonymous-codon | ARNT | GRCh38.p7 | 1:150829150 | AAAAGTGAAGATACC[C/T]TCAATGTTGTGTCGG | 405 |
rs375762141 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150817878 | GCAAATGACCACCCC[C/G]TGGGTGACTGCTCAA | 405 |
rs375818944 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150860627 | TTGGGAGGCCAAGGC[A/G]GGCATATCACCTGAG | 405 |
rs375834336 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150832664 | AGGACCAGATAGTAC[A/G]TATTTTCAGCTTTGC | 405 |
rs375846904 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | ARNT | GRCh38.p7 | 1:150817393 | TGGCCAGTCCATCTC[C/T]TCCTGGTACCATGTC | 405 |
rs376009144 | snp | C/T | 6.59457e-05 | 0.00574182 | missense | ARNT | GRCh38.p7 | 1:150817094 | TACCCGCATTGATGT[C/T]GTGATAGATTTCTGA | 405 |
rs376024237 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150871426 | CCGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 405 |
rs376033110 | snp | G/T | 0.000137071 | 0.00827748 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858476 | CTGTCAGGAAAATAA[G/T]GAAGTAAACATTTTT | 405 |
rs376051428 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809837 | GGCAACGCCCACCCC[A/C]AAACCCCCACCTCAT | 405 |
rs376110918 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150850725 | TGGGAAGTGAGGAGC[A/G]TCTCTGCCTGGCCGC | 405 |
rs376139724 | snp | A/G | 0.000148386 | 0.00861227 | synonymous-codon | ARNT | GRCh38.p7 | 1:150816331 | GGGGTTGGAGTGGCG[A/G]GAAATCTGGGCCAAC | 405 |
rs376140549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150813692 | TCTTGTTGCCCAGGC[C/T]GGAGTGCAAAGGCGC | 405 |
rs376169622 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150862355 | TATACCAATTTAAAG[C/G]CTCATCCACTGCATC | 405 |
rs376287026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150827002 | TCAGCTGGGGACCTG[A/G]ATTTTATTTCTTCTG | 405 |
rs376287624 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858340 | TAACACACTACACTC[-/C]AAACTCACCCTGGTC | 405 |
rs376327095 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150831620 | TGAATCATTTTCCAG[C/G]CTGAGTTATCTATCT | 405 |
rs376342449 | snp | A/G | 5.38769e-05 | 0.00518995 | intron-variant | ARNT | GRCh38.p7 | 1:150846215 | CTGTCTGGTTCTACA[A/G]CATGGATCATATTAT | 405 |
rs376479221 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150829495 | ACATACTGGCTATGC[C/T]GAACTCATTACTCAG | 405 |
rs376550800 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150848702 | TCCAGCTAATTTTTG[C/T]AACATTTTTTGTACA | 405 |
rs376557844 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150851611 | CTCAGGGTTAAATGG[A/C]TTAAGGGCGGTGCAA | 405 |
rs376612759 | in-del | -/GATACA | | | intron-variant | ARNT | GRCh38.p7 | 1:150835819 | AAGAACAACAGTACA[-/GATACA]AACAACAACAACAAC | 405 |
rs376658841 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150861604 | CATTTGAGTCCAGAA[G/T]TTCAAGACCACCCTG | 405 |
rs376661985 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150814650 | AGTTCCAGACCAGCC[A/G]GGCCAACATGGTGAA | 405 |
rs376729294 | snp | C/T | 8.24436e-05 | 0.00641989 | intron-variant | ARNT | GRCh38.p7 | 1:150817452 | TATGTCAAAGGCCAG[C/T]TGACAAGACAAATAG | 405 |
rs376740773 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820871 | ATATTATGAAATACA[A/G]CTGATTGCTCAACAT | 405 |
rs376856896 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | ARNT | GRCh38.p7 | 1:150841309 | ACTTGAACAAAAGTT[A/C]TTTGTCCAAAAAAAA | 405 |
rs376877703 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150835138 | AGCAAGACCTTGTCT[A/C]AAAAAAAAAAAAAAG | 405 |
rs376906243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842118 | AGCACCAACTGGCAC[A/G]GTTGCATTCCTTCTA | 405 |
rs376925279 | snp | A/G | 1.64827e-05 | 0.00287073 | missense | ARNT | GRCh38.p7 | 1:150814097 | TTAGATCCACGATTG[A/G]TGAGACTAGGGTAGG | 405 |
rs377050198 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150860196 | GTGAAAAGGCAACCC[A/G]TGGAATAGAAAAAAA | 405 |
rs377056322 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839542 | TGCGTAAGATGGTTA[A/G]CTTGTCTGGTTTTCG | 405 |
rs377065464 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150847325 | AGTCCCAGCTACTTC[A/G]GAGGCTGAGGCAGCA | 405 |
rs377081259 | snp | C/G | 0.000438862 | 0.0148067 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811997 | ATTTTTTCTCCCCCA[C/G]CCCTTATCCTCACCC | 405 |
rs377082814 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150848065 | TGTAAAAAAAACTGA[A/G]GAGATAAGTGTGTGT | 405 |
rs377116195 | in-del | -/TACA | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811476 | ACACACACACACACA[-/TACA]CATACACACACACTC | 405 |
rs377165214 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835612 | TCTTTTTTGGGTGGG[A/G]AAAAAGGAGGAAAAC | 405 |
rs377175075 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant, missense | ARNT | GRCh38.p7 | 1:150852821 | CCTGAGGAAAGCCAA[A/C]AATAAATACTTTAAG | 405 |
rs377187565 | snp | A/G | 3.29745e-05 | 0.00406031 | intron-variant | ARNT | GRCh38.p7 | 1:150816223 | CCAAACAAACAAAAA[A/G]TAATACACAGGGAAC | 405 |
rs377211645 | snp | C/T | 0.00548854 | 0.0520975 | intron-variant | ARNT | GRCh38.p7 | 1:150816748 | TCAGCAGCTGAATCC[C/T]TCAGGGCCCTGTAAA | 405 |
rs377246409 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150847447 | AAAAAAAAAAAAAAA[-/G]AAGGGGGAAAGGGAA | 405 |
rs377248105 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824611 | AGGCGTGCACCATCA[C/T]GCCCAGCTAATTTTT | 405 |
rs377270748 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150851446 | GGGAAAAGATAGAGA[A/G]ATCAGATTGTTGCTG | 405 |
rs377274345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835071 | AGTTTGAGGCTGTAG[C/T]GTGCTATGACTGTGC | 405 |
rs377304964 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872637 | TGTTCCCTCAGCCAA[C/T]GCATTACAAATGACA | 405 |
rs377410867 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150845263 | GTACTCCAGCCTGGG[A/G]AACACAATGAAAACA | 405 |
rs377417202 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854749 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAT | 405 |
rs377425210 | snp | A/G | 6.87073e-05 | 0.00586079 | intron-variant | ARNT | GRCh38.p7 | 1:150816780 | CAGCACATATATACG[A/G]GGCTCACCTGAAATT | 405 |
rs377528777 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863397 | AATTCAGAGAAGATA[A/G]TCCTGGTTTAAATTA | 405 |
rs377533771 | snp | C/G | 0.000117751 | 0.00767213 | intron-variant | ARNT | GRCh38.p7 | 1:150823156 | TGTTGTGAGAACAGA[C/G]GAAAAACAGTTTTTT | 405 |
rs377579816 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150835694 | TACCAGTTTTTTTAT[C/T]TGCTTCCACTTTAAA | 405 |
rs377671724 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840709 | GATGATTAAAGGTCT[G/T]ACAAGACAATTTGAA | 405 |
rs377688526 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858320 | GGTTTATAGGAGAGA[G/T]ATTCATAACACACTA | 405 |
rs377737236 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872753 | AGATCACTTGAGGCC[A/T]GGAGTTAAAGACCAG | 405 |
rs377744665 | snp | C/T | 0.00014958 | 0.00864683 | intron-variant | ARNT | GRCh38.p7 | 1:150842413 | CATGCTAAAAGACAC[C/T]GTTCTCCTACCTGGC | 405 |
rs377762077 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150828851 | CTGTATTAATATCAA[-/C]AACAAAAAATAAATA | 405 |
rs386635382 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARNT | GRCh38.p7 | 1:150813674 | TTTGAGACGGAGTTT[CA/TG]CTCTTGTTGCCCAGG | 405 |
rs397765787 | in-del | -/A | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150815880 | AAAAAAAAAAAAAAA[-/A]GAATTTTTCAACTTT | 405 |
rs397767768 | in-del | -/A | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150831941 | AAAAAAAAAAAAAAA[-/A]TCTACCCGTAAAACT | 405 |
rs397860863 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150823568 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCCC | 405 |
rs397861462 | in-del | -/C/T | 0.000175485 | 0.00936545 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876605 | GCGCCACCCCCCCCC[-/C/T]AGTGGGAGGAGCCGC | 405 |
rs397862521 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150817831 | AAAAAAAAAAAAAAA[-/A]TTAACCAACCGAACA | 405 |
rs397862771 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150819237 | ACAATAAAAAAAAAA[-/A]GGCAATAACAAGTGT | 405 |
rs397862938 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828365 | GTTTTTTTTTTTTTT[-/T]GCATACAGATATCCA | 405 |
rs397863444 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828364 | TGTTTTTTTTTTTTT[-/T]TGCATACAGATATCC | 405 |
rs397952523 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150867231 | AACAACAAAAAAAAA[-/A]CAGATTACTCAAATA | 405 |
rs397981527 | in-del | -/A | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150835152 | CAAAAAAAAAAAAAA[-/A]GAATAAAAAGAAAAA | 405 |
rs398103239 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150861339 | ATCGCAAAAAAAAAA[-/A]TTAAATTAAAAATAG | 405 |
rs532705909 | snp | A/G | | | synonymous-codon | ARNT | GRCh38.p7 | 1:150831867 | GTGGACCACCACGAA[A/G]TGAGGTTCCCCATCC | 405 |
rs561409178 | in-del | -/AAAAAAAAAA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809647 | CACAAAAAAAAAAAA[-/AAAAAAAAAA]GTTGCTAATGAACCA | 405 |
rs587593534 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150824637 | TTTTTGTATTTTTAG[C/T]AGAGACGGGTTTTCA | 405 |
rs587593925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846065 | CACTGTATAAAATAT[A/G]CCGCCAGTTTGAAGC | 405 |
rs587594417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850406 | CCTGCCTCAGCCTGC[C/T]GAGTGCCTGCGATTG | 405 |
rs587594515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825679 | CGTGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 405 |
rs587594531 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810328 | TTATAGTCCTGATCA[C/T]ATTTAAAAAGTCGAT | 405 |
rs587594635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862164 | TAGTACTCTGTACTA[C/T]AAATGTATAGTTATG | 405 |
rs587594642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837559 | TCTTCTATGAGACTG[C/T]ACTCCAATTTTTGCT | 405 |
rs587594748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836777 | CTAGGCACAGCGGCT[C/T]CCGCCGGTAATCCCA | 405 |
rs587594753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862944 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 405 |
rs587595736 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150849840 | GAAGCTGAGGCAGGT[A/G]GACCACTTAAGGCCA | 405 |
rs587595774 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150850438 | AGTCGCGCGCCGCCA[C/T]GCCTGACTGGTTTTC | 405 |
rs587595862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812331 | CACCTTTTTCCTTTT[C/T]CTAGTTCTCAATATT | 405 |
rs587595966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867066 | CAAAAAATTAGCCAG[G/T]CGTGGTGGCACACTG | 405 |
rs587596055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871887 | CACTCCAGCCTGGGC[A/G]ACACAGTAAGACCCT | 405 |
rs587596098 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878736 | GGCTGTAATCCCAGC[A/T]CTTTGGGAGGCCAAG | 405 |
rs587596110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819215 | AATTGATACCTACTA[C/G]ATGGCTACAATAAAA | 405 |
rs587596428 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811664 | CTTTCCAAAAACAAG[C/T]CATACTATCCAAGGC | 405 |
rs587596464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823990 | TGAGATTATAGGCAC[A/G]TGCCACCACGCCCAG | 405 |
rs587596489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150820649 | GTGCCAGAGCGAGAC[C/T]CTGTCTGAAAAAACA | 405 |
rs587596495 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877562 | ATTGGAGGCAATAGA[G/T]GAAGAAAGTAATTTG | 405 |
rs587596669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150831358 | CATTCCTTGTTTGAC[C/G]TCAAGTTCTGGTAAA | 405 |
rs587596988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150832251 | GAGCTGCTGAAGGAA[C/T]GACTACAGTAAGACA | 405 |
rs587597346 | in-del | -/TTTT | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150854097 | CTCTTCCTTTCTTTC[-/TTTT]TAAGAGACAAGCTCT | 405 |
rs587597391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150861175 | GAAATGTAAAATGGC[A/G]TAACAGCAATAGAAA | 405 |
rs587597506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150860537 | AAAATTTTCGAATCA[C/T]ATATGCAACACAGAA | 405 |
rs587597706 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858256 | GAAGTGAGATGGTCA[A/G]GAATAGCGAAGTGAG | 405 |
rs587597713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841105 | AGGCGCACACCACCA[C/T]GCCCAGTTTTTTTTT | 405 |
rs587597863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851619 | TAAATGGATTAAGGG[C/T]GGTGCAAGATGTGCT | 405 |
rs587597909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874464 | ACTGAGGCAAGGCTT[G/T]CTTGAGACCAGGAGA | 405 |
rs587597959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823437 | CTATAACCCTAAAAC[C/T]CTTGTCATTGTCCTT | 405 |
rs587598019 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150871682 | TGGGAGGCCAAGGTG[A/G]GCGGATCACCTGAGG | 405 |
rs587598179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150856267 | ACACGGTGAAACCCC[A/G]TCTCTACTGAAAATA | 405 |
rs587598437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813954 | TTCTAAATAGATTGT[A/C]ACCTTGCATTTCCCT | 405 |
rs587598734 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150847248 | CCACTCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 405 |
rs587598874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868939 | AAAAGGACCAGCCTG[C/G]GCAACATAGCGAGAT | 405 |
rs587599005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816550 | AATTTGGAAAAGACA[A/G]GAAAGACTGACAGTC | 405 |
rs587599025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150813428 | AACTATAGGTAAGCC[A/G]TTAATTTTACCTAGG | 405 |
rs587599174 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876738 | AGCCCCCAGCATCCC[A/G]GCCCCTGCGGCGGGG | 405 |
rs587599220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854391 | GGTGAAATCCCGTCT[C/G]TACAAAACATACAAA | 405 |
rs587599564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862866 | GACCAGCCTGGCCAA[A/T]ATGGTGAAACTCCGT | 405 |
rs587599690 | in-del | -/A | 0.405082 | 0.196086 | intron-variant | ARNT | GRCh38.p7 | 1:150864884 | GGTTTTCTTTAAATC[-/A]AAAAAAAAAAAAAAA | 405 |
rs587600249 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150860145 | CATACTGTATAGTGT[A/G]CAATATTTTGTGCAT | 405 |
rs587600295 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811367 | CTTAGGACTCTTTGA[A/G]AAGTACACAGAAAGA | 405 |
rs587600384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848920 | AATAAGAAAAAGAAA[C/T]GGGCCGGGTGTGGTG | 405 |
rs587600542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150831101 | GGTCAAGCAACTTAC[C/T]CTAGGTGATGCCACT | 405 |
rs587600720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849684 | GGGAGGATCGCTTGA[G/T]CCCTGGAGTTCGAGG | 405 |
rs587600949 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150870784 | AAAGTGCTAGGATTA[C/T]AGGTATGAGCCACCA | 405 |
rs587601021 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARNT | GRCh38.p7 | 1:150850917 | TGGGAGGTGAGGAGC[A/G]CCTCTGCCCGGCCAC | 405 |
rs587601319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838713 | TTCTGCAATGATCAT[A/G]TTATTTTAATAACCA | 405 |
rs587601654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864526 | ATCAAAAAACCAAAC[A/C]CCGCATATTCTCACT | 405 |
rs587601947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150833620 | CTCAGTACAATGTAG[C/T]CAATTTCCATTATAT | 405 |
rs587602197 | in-del | -/CA | 0.000362797 | 0.0134635 | intron-variant | ARNT | GRCh38.p7 | 1:150839419 | GATTCCAGACTCTCT[-/CA]GAACTATAAGTCCCA | 405 |
rs587602215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866854 | ACAGAAAGGTAGGAA[A/G]AACAGCAGATTTAAA | 405 |
rs587602231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150814871 | AAAAAAAGTACCATA[C/T]GCAGAGAAAAACTAC | 405 |
rs587603021 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150863646 | CCAGCCTGACCAACA[A/T]GGTGAAACCCCGTCT | 405 |
rs587603285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847048 | TACTTCGACCTCTTA[C/T]CTATTGCGCAAAATG | 405 |
rs587603318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150843154 | TTATTAACTTTGATT[C/T]GGTCCTTTTGCCATT | 405 |
rs587603374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830219 | GGCATGGTGGCATGC[A/C]CCTGTAATCCCAGCT | 405 |
rs587603446 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150835580 | TACTCCAGCCTAGGC[A/T]AGAGAGAGACCCTGT | 405 |
rs587603610 | snp | C/T | 0.000118547 | 0.007698 | intron-variant | ARNT | GRCh38.p7 | 1:150876532 | GGCGCCCCAGTCCTC[C/T]GTCTCCTCACCGGGG | 405 |
rs587603632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150834880 | ATTGTGCAAGGAAAA[C/G]TAGGAGTGGAAAGTA | 405 |
rs587603718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835793 | GAACATAATAAAATA[A/G]GGGAGAAAAAAAGAA | 405 |
rs587604107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843272 | TTCTAGAAAACTGAG[A/G]TACTGTAATGATGGG | 405 |
rs587604205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830087 | TTATGGGCCAGGCAC[C/T]GTGGCTGACGCCTGT | 405 |
rs587604522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812519 | ATTCACTCTTGCAGT[C/T]CCTCAGGACTTGTGT | 405 |
rs587605136 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823316 | GAACCGGAACATGAC[A/G]GACAGCACTTGGCCT | 405 |
rs587605180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842294 | ACTCAAACTTCTAAA[A/G]AATCTTGTCCTCTCT | 405 |
rs587605416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838552 | TAAGTAGACCATCCT[A/G]TTTGGAAAATTCTTA | 405 |
rs587605454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862075 | GTACTTATTCTGAAC[C/T]TTTTCCCTTCCACGT | 405 |
rs587605667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821432 | TACTGGAGTGAATTG[A/C]TCATGAAGAGATGAT | 405 |
rs587605778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860530 | AGAAAAAAAAATTTT[C/T]GAATCATATATGCAA | 405 |
rs587605786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839412 | TCACCCAGATTCCAG[A/G]CTCTCTCAGAACTAT | 405 |
rs587606472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822545 | ATGGAGATCCCCGGA[C/G]GGTAGCCCACCCAGA | 405 |
rs587606481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875784 | TTTTGAAATTGAGAA[A/G]TGGTGTGGAATCAAA | 405 |
rs587606689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842964 | AGTACATTAAAGATG[A/G]TACTATCAAACAAGT | 405 |
rs587607234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870735 | GCTGGTCTCAAACTT[C/T]TGGGCTCAAGCAATC | 405 |
rs587607306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862994 | AGGCGGAGGTTGCAA[C/T]GAGCCAAGATCGTGC | 405 |
rs587607313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836704 | CCTCACTTTCTCTAT[G/T]TCACTATCCACCTCT | 405 |
rs587607515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858151 | AAAAGAACTGCTTAC[A/G]GGAAACTTGGATAAA | 405 |
rs587608004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817526 | AAAACAAATTAAACA[A/G]GCCGGGCATGGTGGC | 405 |
rs587608052 | snp | A/G | 3.295e-05 | 0.00405881 | missense | ARNT | GRCh38.p7 | 1:150814128 | CAGCAGCACCAGGCG[A/G]TGCAGTTGGGGCACC | 405 |
rs587608175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150839221 | ATATTCATGAGTCAA[A/G]TTCTCAAATATTAAT | 405 |
rs587608277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815020 | AAAATATAAAGAAAA[G/T]AAGAATCATTCATAA | 405 |
rs587608382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875858 | AAGATTTAAACCTGG[A/G]GCTGTGGAACTAAAG | 405 |
rs587608465 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150821695 | CCTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGTG | 405 |
rs587609342 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150850045 | CAACAGAGGAAGACT[C/G]TGTCTCAAAAAAACA | 405 |
rs587609348 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150850429 | TGCGATTGCAGTCGC[A/G]CGCCGCCACGCCTGA | 405 |
rs587609512 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811515 | TTACTCACATGTTTC[C/T]TTCCAGAGGGACTGC | 405 |
rs587609722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853519 | CTGAAACATCTTTCA[A/C]AGCAGTGATCTTACA | 405 |
rs587609753 | snp | A/G | 0.000683293 | 0.0184711 | intron-variant | ARNT | GRCh38.p7 | 1:150861243 | TGGGTGCAGTGGTGC[A/G]CACCTGTAGTCCCAG | 405 |
rs587609883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853817 | TTATAAACAATAAAA[C/T]AGACCAATCCCCTTA | 405 |
rs587609944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830368 | AAAAAAACCAAAAAG[C/T]AAAACAAAACAAAAT | 405 |
rs587610051 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877894 | TCTCACAAACTGTTG[A/G]GATTACAGGCGTGAG | 405 |
rs587610188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150846459 | AACAGCAGCACCCCA[C/T]AGAACTTAAAAGACC | 405 |
rs587610210 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150871027 | ATAAAAACTTTAAAA[C/G]AAGAAAATACATTGA | 405 |
rs587610463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150826363 | AGCCAAACAGAAATA[C/T]CTTGGGCATTATCCA | 405 |
rs587610715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843948 | TACTACTACTACTAC[C/T]ACAGATCCACAATCC | 405 |
rs587611180 | snp | C/T | 3.30726e-05 | 0.00406635 | intron-variant | ARNT | GRCh38.p7 | 1:150852756 | GAAAGTTTTTCAGTC[C/T]CTTACCTCAAAAATT | 405 |
rs587611292 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150868345 | TCAAGGGTGAGAAGA[C/G]AAAAGTAGAAGCATA | 405 |
rs587611638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856562 | GAGGTCAGGAGTTCG[A/C]GACCAGCCTGGCCAA | 405 |
rs587612331 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876668 | AGGCCACTCCCCAGA[A/G]GCGGCGCCTGACCGC | 405 |
rs587612663 | snp | C/G | 0.021333 | 0.101051 | intron-variant | ARNT | GRCh38.p7 | 1:150864669 | CTAATGCTAGATGAC[C/G]AGTTAGTGGGTGCAG | 405 |
rs587612751 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810646 | TTAAAAAAAAAAAAA[A/G]AAAAGCTGGTATCTA | 405 |
rs587612923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150820788 | AAAGTAGAGGAGAAA[C/G]GGATAGCTTGATAAG | 405 |
rs587613001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863151 | GGTAGATCACTTAAG[A/G]TCAAGTTTGAGACCA | 405 |
rs587613128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872990 | ATGTGTTCCTCAAAA[C/T]TTGTCTAGTCCGGGC | 405 |
rs587613147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150834087 | TATGGGCGCACGCCA[A/C]CACGCCCGTCTAATT | 405 |
rs587613171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868557 | TGCCTGTAATCTCAG[C/G]AATCTGGGAGGCCAA | 405 |
rs587613314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861380 | TGATCCAGCAATTCC[A/G]CCTCTGGGTATATAC | 405 |
rs587613381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854793 | ACCCGGGAGGCAGAG[G/T]TTGCAGTGAGCCAAA | 405 |
rs587613405 | snp | A/C/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150815598 | GGCGCGGTGGCTCAC[A/C/G]CCTGTAATCCCAGCA | 405 |
rs587613451 | snp | A/C | 1.738e-05 | 0.00294783 | intron-variant | ARNT | GRCh38.p7 | 1:150846247 | TATTACAATATATTA[A/C]CTACTACAATATTAC | 405 |
rs587613753 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150851082 | AGTGAGGAGCCCCTC[C/T]GCCCCGCAGCCGCCC | 405 |
rs587613820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824198 | CATTTTTTGCCATTT[A/T]AAAAAATGGCAAAAA | 405 |
rs587613864 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877075 | CGAAACCAGCCTGGC[C/T]AACATGGCGAAACCC | 405 |
rs587614041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150841292 | TACCACTTAAGAATT[C/T]TACTTGAACAAAAGT | 405 |
rs587614143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858767 | GCTAGGACTATAGGC[C/T]CGCACTACCACACCC | 405 |
rs587614413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150840453 | AAGAATTGATAGTAC[A/G]GATTTCCTTGGTCTA | 405 |
rs587614663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867311 | AAGATGGGGGGACTA[C/T]TTGAGCTCAGCAGTT | 405 |
rs587614788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818352 | AAAAAAATGAAAGTA[C/T]ATACACTGTACATCA | 405 |
rs587614874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870371 | TGGGTTTTACATTCA[C/T]TTTTATTCCACAAAC | 405 |
rs587614891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857807 | TAATTATTTCTATCA[A/G]AACACAACCAACTTA | 405 |
rs587614994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866044 | CTGGTGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 405 |
rs587615085 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809516 | TGGGAAGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 405 |
rs587615471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150850112 | TTAACAACTCAAAAA[C/T]ACAAATTCCTCACAC | 405 |
rs587615808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857404 | CTTACTAGCTTTACA[A/G]TCTTAGAAAGTTACT | 405 |
rs587615843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854285 | AATCTCAGCCAGGCA[A/T]GGTTGCTCACACCTG | 405 |
rs587615892 | snp | A/G | 1.64906e-05 | 0.00287142 | intron-variant | ARNT | GRCh38.p7 | 1:150816211 | ACGGAAAAAAGCCCA[A/G]ACAAACAAAAAATAA | 405 |
rs587615991 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150873865 | TTCAAGGCTACAGTG[A/G]GCTGTGATTACACCA | 405 |
rs587616154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150860309 | CAACCTCCAACTCTC[A/G]GGTTCAAGTGATTCT | 405 |
rs587616799 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150864145 | AACTATAACTCAGTG[C/G]TAACTATTTATGTAT | 405 |
rs587616849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812666 | TCTCTATATTCATTC[A/C]AATTTTAGTATATAT | 405 |
rs587616945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843650 | TTAACAAACTACAAA[C/T]TTCTTTTTTTTCAAA | 405 |
rs587617267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824397 | AGAATATAGCTTATA[C/T]ATTGCTCTTCAATCC | 405 |
rs587617348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823515 | AAGTGATTAAACATG[A/G]AAGCATATTTCTCAT | 405 |
rs587617446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841010 | CTGGAGTACAGTGGC[A/G]GGATCTCGGCTCACT | 405 |
rs587617516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826835 | TTTTTTAAATAGAGA[C/T]AGGGTTTCACCATGT | 405 |
rs587617711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862269 | CTTCCATATTATTTC[C/T]GAAAATGACTCCCTG | 405 |
rs587617818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866265 | TGGGATTACAGGCGT[A/G]AGCCACCAAGGTCAG | 405 |
rs587617916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843595 | ATATTCAGCAGTTTA[A/G]AGTTTTACATTCCTT | 405 |
rs587617967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870559 | GTCACCCAGACAGGA[A/C]TGCAGTGGCACAATC | 405 |
rs587618209 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150840718 | GGTCTGACAAGACAA[-/T]TTTGAATCTCACCCA | 405 |
rs587618442 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150838255 | TGCTCAAGTGCTTCC[C/G]AAAATCCACAACACT | 405 |
rs587618470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827875 | CTAGTGGGTATATAG[C/T]GGTATCTCATTGTGA | 405 |
rs587618780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872154 | GTAGTAAAGGGGTTT[C/T]GTCACGTTGTCCGGG | 405 |
rs587619278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150873447 | GAAGAATTATCAATT[C/T]GAGAAAAAAAATCAT | 405 |
rs587619472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150840133 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGACAG | 405 |
rs587619661 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809983 | ACACAATGTGCCTTA[A/T]GTTTGTATGTCTGGA | 405 |
rs587619763 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARNT | GRCh38.p7 | 1:150851702 | CCTAATCTCAAGTAC[C/T]CAGGGACACAAACAC | 405 |
rs587619967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819817 | CTAGAATTTCTTTTG[C/G]GGGAATGAAAATATT | 405 |
rs587620056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867886 | TGCTTGCTTCCCCTT[C/T]GCCTTCCGCCATGAT | 405 |
rs587620187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845745 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 405 |
rs587620449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828903 | CACCTGGTTTGACAA[A/G]CCATATTTCTCTACA | 405 |
rs587620586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862248 | CTTCATGCACAGGTG[C/T]CAGTACTTCCATATT | 405 |
rs587621197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827135 | CTTCTAAAACATTTT[C/T]CTTTCTCAGAATATT | 405 |
rs587621224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826435 | AGATTAACTACTAAA[G/T]AACATAAAACTGTAG | 405 |
rs587621669 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150860760 | ACTCGGGAAGCTGAG[G/T]CAGGGAGAATTAATT | 405 |
rs587621798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858704 | ATAGGTCACTACAGC[C/G]TCAAACTCCTGGGCT | 405 |
rs587622151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837000 | GAGCCTGGGAAGCAG[A/G]GGTTGCAGTGAGCCG | 405 |
rs587622356 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878108 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 405 |
rs587622473 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877177 | TGAGGCAGGAGAATC[C/G]CTTGAACCTGGGAGG | 405 |
rs587622521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855719 | CCAGCCTGGTCAACG[A/T]AGTGAGACCATGTCT | 405 |
rs587622626 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811732 | ATCTCAGCACAAATC[A/G]ACACTATACAATTTC | 405 |
rs587622938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825814 | AGATTGCACACTACA[C/T]TCCACCCTGGCGACA | 405 |
rs587623352 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARNT | GRCh38.p7 | 1:150851438 | GAAATGTGGGGAAAA[A/G]ATAGAGAAATCAGAT | 405 |
rs587623358 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARNT | GRCh38.p7 | 1:150848122 | AATTCTATATATACT[A/G]TTTTTGGAAGGATAC | 405 |
rs587623384 | snp | C/T | 3.31257e-05 | 0.00406962 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813196 | CTCAGGCTGGCCAGG[C/T]TGCTGTGCTGGCGGT | 405 |
rs587623629 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150870074 | TAACTTGGAGATTAA[A/G]AATGATGACTGTGTA | 405 |
rs587623817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869349 | GGGCATGGTGGTGGA[C/T]GCCTGTAGTCCCAGC | 405 |
rs587623964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817668 | CAAAAAATTAGCCGG[G/T]GGTGGTGGCAGGCAC | 405 |
rs587624123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871215 | TTAAGTGTAAAATGA[C/T]AGGTGTTGTCATATT | 405 |
rs587624229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150832679 | ATATTTTCAGCTTTG[C/T]GGGCCAGAAAGTCTG | 405 |
rs587624472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844939 | CTCAGCCTCTAGAGT[A/G]GCTGGGATTATGAGT | 405 |
rs587624534 | snp | A/G | 6.58957e-05 | 0.00573964 | missense | ARNT | GRCh38.p7 | 1:150816279 | CAGAAAAGCCTGAGC[A/G]GGTAGTAGGGGTCCA | 405 |
rs587624631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150874630 | GAGGTGGAGGCTGCC[A/G]TGAGCAGTGATCTTG | 405 |
rs587625203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844172 | TAGAGATGGTTCACA[A/T]CCTAAAGACTTTACA | 405 |
rs587625208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855501 | CAGGAGGCGGAGCTT[A/G]CAGTGAGCCAAGATC | 405 |
rs587625714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150836099 | AAATATTTTCTAAGG[C/T]TGAGCCACAAAGTAG | 405 |
rs587625737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861626 | ACCACCCTGGGCAAC[A/C]CAGTGAGACCCTATC | 405 |
rs587625809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864992 | TGGATCAGATTCAAC[A/G]AAGACAAACATATAA | 405 |
rs587625939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844618 | TATTCATCTTTCTGA[A/G]GTAGCTACAAACTTA | 405 |
rs587626110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838328 | TTACAGCACTTCTAT[A/T]ATAGAACTAGTTCTA | 405 |
rs587626361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833012 | TGTTCTAAATATCTT[C/T]ACATATATTAATTCA | 405 |
rs587626458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824201 | TTTTTGCCATTTAAA[A/T]AAATGGCAAAAAATC | 405 |
rs587626641 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857127 | TTTTTTCCTATGTAC[-/AT]GTTATACATATCTTT | 405 |
rs587626724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845674 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACAAGG | 405 |
rs587627434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873510 | GAGTACCAACCATAT[C/T]TTACTCTTCTTCTAA | 405 |
rs587627508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866931 | CAAATAGAGGCTGGG[C/T]GCAATGGCTCACACT | 405 |
rs587627791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856397 | GTGAGCTGAGATCAC[A/G]CTACTGCACTCCAGC | 405 |
rs587627934 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810857 | GAAAAACCTCTTAGG[A/G]CCAGAGAGACTTAAA | 405 |
rs587628271 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | ARNT | GRCh38.p7 | 1:150851665 | TTGAAGGCAGCATGC[G/T]CATTAAGAGTCATCA | 405 |
rs587628379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150824791 | ATCTACAGAGGTTTC[C/T]ATAAATAAAATTAAG | 405 |
rs587628462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841241 | AAGCATGAGCCACTG[C/T]GCCCGGCCTGCTTTA | 405 |
rs587628598 | snp | C/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150873697 | GCTAAGGTGGGAGGA[C/T]TGCTTGAGGACAGGA | 405 |
rs587628638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851099 | CCCCGCAGCCGCCCC[A/G]TCCGGGAAGTGAGGA | 405 |
rs587628747 | snp | A/G | 0.000232238 | 0.0107733 | synonymous-codon | ARNT | GRCh38.p7 | 1:150816811 | CTCTGCCGGCCGGGG[A/G]GTAGGAGGGAATGTG | 405 |
rs587628855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841512 | TCGAGTTAAACTGGC[A/G]GCAAAATGAGTTTGT | 405 |
rs587628985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817764 | CAGTGAGCCTAGATC[A/G]TGCCATTGTATTCCA | 405 |
rs587629750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860481 | TCAGCCTCCCAAAAT[A/G]CTAGGATTACAGGCA | 405 |
rs587630129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150840319 | ACTCACTTAAGTTCC[C/T]ATGGAACATATAACC | 405 |
rs587630543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837027 | GCCGAGATCATACCA[C/T]CACACTCCAGCCTGA | 405 |
rs587631180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150861835 | ACCATTACAATTTCA[A/G]TGTAATGTACAGTGT | 405 |
rs587631327 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150836741 | TATCTCAGGATTCAA[-/G]GAAGAATAAAAAGGC | 405 |
rs587631427 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARNT | GRCh38.p7 | 1:150851272 | CAGCCGCCGCCCCGT[C/T]CGGGAGGTGGGGGGC | 405 |
rs587631511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860023 | AAAAAAAAAAAGGGT[A/G]CATTTTTCTCTTAGT | 405 |
rs587631605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150813857 | GGTTGAACTCCCAAC[C/T]TCAAGTGATCCGCCT | 405 |
rs587631678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870173 | ATTCACTCTCTGTGC[C/T]TTAGTTTCCTCATCT | 405 |
rs587631921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823577 | TTTTTTTGAGACGGA[G/T]TCTCCCTCTGTCGCC | 405 |
rs587631945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845780 | GGTGGCAGGGGCCTA[C/T]AATCCCAGCTACTCA | 405 |
rs587632224 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150832571 | TCTAAAACTTTTAGA[A/C]TTTGAAGTCAAAATG | 405 |
rs587632313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853018 | AGGAGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 405 |
rs587632654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816962 | CAGCAAGTTCCTATT[G/T]ACTCAGGTGGTATTA | 405 |
rs587632900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847747 | ATTCTCAATAAAGCT[C/G]TTTGAAAAAGTCTAT | 405 |
rs587633074 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150876450 | CCCCGGCGCCTTCAG[C/T]TCCAGCTGCGTCCCC | 405 |
rs587633088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853208 | ATTGCTGGAACCCGG[A/G]AGGTGGAGGTTTCAG | 405 |
rs587633933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150833934 | TCATTTCTTTTTCTT[C/T]TTCTTTTTTTTTTTT | 405 |
rs587633989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150874691 | AGGAGCAAGACCCTG[C/T]AGCAAAAGAAAAAGA | 405 |
rs587634425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150864027 | ACTACACACCTAGGT[A/G]TGTAGGTGTATAGCC | 405 |
rs587634606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867835 | GTGTAGCACCTTCCC[C/T]TTCTCTCCCTCTATC | 405 |
rs587634863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150820918 | GACCCCTGTGCCATC[A/G]AAAATTCGACTGTAA | 405 |
rs587634911 | snp | A/C | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150830038 | CTCAAATGCCTTCAA[A/C]ACTCAGACAAGTAAA | 405 |
rs587635075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813906 | GCTGGTATTACAGGC[A/G]TGAGCCACCGCACCC | 405 |
rs587635162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150869694 | TTGGGACTATAGGCA[C/T]CCACCACCACATCTA | 405 |
rs587635179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860420 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTT | 405 |
rs587635369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824002 | CACGTGCCACCACGC[C/T]CAGCTAATTTTTGTA | 405 |
rs587635403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150864243 | GAATTTTTCATCTCC[A/G]TTATAATCTTATGGG | 405 |
rs587635516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812610 | AAATGGAACACTTCA[A/T]GAATTTGTGTGTCAT | 405 |
rs587635540 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811791 | TAACTTCACCCAGCC[A/T]CAAATTTTCAGACAG | 405 |
rs587635644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835893 | ATCTATAGAATAAAA[A/G]GCTGTTATCATTGAA | 405 |
rs587636187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825647 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCCA | 405 |
rs587636206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150852277 | TAAGCAGAGGCTTGA[C/T]AAGCACTTGCACACT | 405 |
rs587636685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866660 | GTATAGTTTTGATTT[A/C]AATAACTTTTATATA | 405 |
rs587636787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815843 | CACTCTAGCCTGGGC[A/G]ACAGAGCAAGACTCT | 405 |
rs587637003 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150871675 | AGCACTTTGGGAGGC[C/G]AAGGTGGGCGGATCA | 405 |
rs587637065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856255 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 405 |
rs587637093 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878492 | TTTAACAAAAATCCC[A/G]TTATGCTATTGAACA | 405 |
rs587637102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851143 | GCAGCCGCCCCGTCC[A/G]GGAGGTGGGGGGCAG | 405 |
rs587637299 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150862835 | AGGCAGGCAGATCAC[A/G]ACATCAGGAGTTCGA | 405 |
rs587637984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861114 | ATAAATAAATAAAGG[A/G]TTGGCAAGGATGTGG | 405 |
rs587638270 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150821073 | AGCTAAAGAGAAAAT[G/T]TTATTAAGAAAATCA | 405 |
rs587638348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875408 | TCATACTGCCTTTCA[A/G]TAACATGAAAAAAAA | 405 |
rs587638473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150843009 | TCTCTCTCCCTCTCA[C/T]ACAAACAACACATGC | 405 |
rs587638916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850826 | GGCCGCCATCCCGTC[C/T]AGGAAGTGAGGAGGG | 405 |
rs587638940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839907 | CCTGGAAACTTCACA[C/T]CCTTTGTAAATTACC | 405 |
rs587639191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873401 | TCTACTTGCCAGTGA[G/T]AAGTAGAACTAGTGA | 405 |
rs587639387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828163 | AATCCAATTTATAAT[C/T]TTTTTTCTTCTGTGA | 405 |
rs587639883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843543 | AATGTAAAAATTTAC[A/G]CATATATTCTGATGA | 405 |
rs587639902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825379 | TTAATATATTCATTG[C/T]ATCAATAACGACACT | 405 |
rs587640008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833254 | CAGGCCTGTAATCTC[A/T]GCACTTTGGGAGGCT | 405 |
rs587640284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150859460 | CCAGTGATCCTCCTG[C/T]CTCAGCTTCCTAAGT | 405 |
rs587640379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823924 | CTCGGCTCACTACAA[C/T]CTCCGACTCCCTGGT | 405 |
rs587640415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848385 | AGCTTGAACTCAGGA[A/G]GCGGAGGACGCAATG | 405 |
rs587640516 | snp | C/T | 1.66718e-05 | 0.00288715 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150816405 | GGGCTAGGCCACTAT[C/T]CCTAGGAGTGAATAA | 405 |
rs587640607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872781 | CAGCCTGGGCAACAT[A/C]GCAAGACCCTGTCTC | 405 |
rs587640653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812964 | AGCCTTCTAAGGGGC[C/T]GACATCATATACACA | 405 |
rs587641102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813091 | CACCTCAATCCAGGC[A/C]TGCTTCCTTCACTGT | 405 |
rs587641160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150865744 | ATGTATGCATACTAC[A/G]TGCTTCATTTTTCTT | 405 |
rs587641190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839988 | GCTCATGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 405 |
rs587641255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875670 | AGAGGAAAGAGGGCT[G/T]GGACTAGTAATTTGA | 405 |
rs587641280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835514 | CTGTAAGCAGGCAGA[G/T]TACTGAGCCCAGAAG | 405 |
rs587641492 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811291 | CAAGCGCAGCAAAGA[C/T]GTTTATTTAAATATT | 405 |
rs587641663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842560 | AAAGGAAGGAGGGAG[A/G]GAGAGGAAATGGAGG | 405 |
rs587641733 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150851042 | AGTGAGGAGCCCCTC[A/C]GCCCGGCAGCCGCCC | 405 |
rs587641831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847494 | TCAGGCACAACAACC[C/T]GACTTGGTAAGATAA | 405 |
rs587641918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826024 | GTTCAAGTGATTCTC[A/G]TGCCTCAGCCTCCCG | 405 |
rs587641946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848204 | GGGGCAGTGGCCCAC[A/G]CTTGTAATCCCAGCA | 405 |
rs587642399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150814798 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCTA | 405 |
rs587642415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816504 | CCCTAGATCCCCTTG[A/T]CTTCCTGCAGGTTAA | 405 |
rs587642538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865436 | ACCAACTCAATTTAC[C/G]CTATGGAATTCCCCA | 405 |
rs587642770 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150868910 | CTCAAAAAATAATAA[A/T]AAAATTTAAAAAAAA | 405 |
rs587643428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150814919 | TCTGTTCTGCATTCA[C/T]TTGTTCCTAATGATG | 405 |
rs587643554 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810067 | AGGAATGATAAAGCC[A/G]CAATCAAGATCACAC | 405 |
rs587643968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150826736 | TGCAACCTCCACCTC[C/T]TGAGTTCAAGCAATT | 405 |
rs587643980 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150819472 | CTTATCCCTATTTTA[C/G]ATATGGAAGCATTTT | 405 |
rs587644124 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877519 | TCCAGGTGTTAACGG[G/T]TTGGTATGGGAGATA | 405 |
rs587644220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872512 | AAGAATTCTCTGCTA[A/C]TGAGAATACCAGAAT | 405 |
rs587644238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150838619 | AATCATTTGATTAAA[C/T]TGGTGGCATTAAGGG | 405 |
rs587644644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830771 | GAAAGGGAAGAAGAC[C/T]GCATTTCTCCCCTGT | 405 |
rs587644931 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855235 | AAAATAGGAAGTTAA[A/C/G]TACATCCTTTCACGC | 405 |
rs587645091 | snp | A/T | 1.65269e-05 | 0.00287457 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836398 | CTGGTTCAAAACAGG[A/T]GTCACGGAGTCAGAC | 405 |
rs587645347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842216 | TAGCAATTTCTTAAA[A/T]CCCTAAGCAAAGTTC | 405 |
rs587645647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853101 | GCCTGGCCAACATGC[C/T]GAAACCCCATCTCTA | 405 |
rs587645695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854106 | TCTTTCTTTTTAAGA[C/G]ACAAGCTCTCACTCT | 405 |
rs587645752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847330 | CAGCTACTTCGGAGG[C/G]TGAGGCAGCAGAACC | 405 |
rs587645985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818402 | TGAGAATTTTATTCC[C/T]TCTCTTTGTATTTTT | 405 |
rs587646150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866802 | AGTTCCTTAGCCTGG[A/G]GAAATGAAAAACTGA | 405 |
rs587646298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150835564 | CTATGATGTGCCACC[A/G]TACTCCAGCCTAGGC | 405 |
rs587646335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863277 | TGAGGCATGAGAATC[A/G]CCTGGGAGGCAAAGG | 405 |
rs587646728 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150854376 | CAGCCTGGGCAACAC[A/G]GTGAAATCCCGTCTC | 405 |
rs587647063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150832121 | GGTAAAATAGCATAG[C/T]GACTTCCTTAAACAG | 405 |
rs587647213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150845180 | AATCCCAATATTTGG[A/G]AAGCTGAGGTAGGAG | 405 |
rs587647518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866865 | GGAAGAACAGCAGAT[G/T]TAAAGGAAATACTGG | 405 |
rs587647655 | in-del | -/T | 0.16028 | 0.233346 | intron-variant | ARNT | GRCh38.p7 | 1:150813634 | TTTTCATGTGGGTAG[-/T]TTTTTTTTTTTTATT | 405 |
rs587647957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822824 | TACTGCATACACAAA[C/T]TGGGGGATCTGATGC | 405 |
rs587647960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868597 | GATCACTCGAGGACA[G/T]TAGTTCAAGACCAGC | 405 |
rs587648334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813721 | GCGATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC | 405 |
rs587648370 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842924 | ATCCACATGTGCTAT[A/T]CTATAATGAAGAAAT | 405 |
rs587648393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868157 | CTGCTTGGTTTACTA[C/T]TTAGTTCTAGCCCCA | 405 |
rs587648633 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810329 | TATAGTCCTGATCAC[A/T]TTTAAAAAGTCGATT | 405 |
rs587648669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150834355 | AAGCACCTATCATAG[C/T]GTCTGGCAAGTTCAG | 405 |
rs587648799 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARNT | GRCh38.p7 | 1:150850407 | CTGCCTCAGCCTGCC[A/G]AGTGCCTGCGATTGC | 405 |
rs587649187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858144 | GTTTAAAAAAAGAAC[C/T]GCTTACGGGAAACTT | 405 |
rs587649409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838507 | ACATATTAACTATTT[C/T]AATGTATATAGCTAC | 405 |
rs587649664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150851980 | TAGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 405 |
rs587649839 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150846590 | AGCACAATTCTAAAG[A/T]AAGGGGTTAGTTTTG | 405 |
rs587649856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822023 | TATAATAGATTTGTA[C/T]ATGTTGTATGGTAGT | 405 |
rs587649905 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150854725 | AGCTGGGTGTGGTGG[C/T]GGGCACCTGTAATCC | 405 |
rs587650024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822856 | ATCTCCAAGTAGATA[A/G]TGAACTGAATTGAAT | 405 |
rs587650195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850500 | GGTTGGCCGGGCTGG[A/T]CTCCAGCTCCTAACC | 405 |
rs587650608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845377 | AGGCTGAGGTGGGTG[A/G]ATCGCTTGAGGTGAG | 405 |
rs587650701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869804 | ACAATCCTCTCACCC[C/T]GGCCTCTCAAAGTGC | 405 |
rs587650789 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150823867 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 405 |
rs587650898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150873060 | GAGGCCGAGGCAGGC[A/G]GATCACAAGGTCAGG | 405 |
rs587651115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150859109 | ACATACATAAATGGG[C/T]TTATACATTTCATTC | 405 |
rs587651452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856987 | TTTTTAAAGACTTCC[C/T]TTAATATATTTTTCT | 405 |
rs587651611 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857652 | GTGCCCATTCTTCCA[-/G]GCCCCTCTAAGGCAA | 405 |
rs587651645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856446 | CTCCATCTCAAAAAA[A/C]TAAAAAATAAAATAA | 405 |
rs587651665 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150830326 | ACTCCAGCCTGGGCG[A/T]CAGACAGAGTGAGAC | 405 |
rs587651743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851456 | AGAGAAATCAGATTG[G/T]TGCTGTGTCTGTGTA | 405 |
rs587651790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816142 | TGGAAATTGGAAACC[A/G]GAGAACAGGGGTTGG | 405 |
rs587652084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857552 | GGTGGGACAAAACTT[A/G]AAGACTGGTTATAAT | 405 |
rs587652214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860816 | GAACCAAGATCGCAC[C/T]ACTGCACTCCAGCCT | 405 |
rs587652390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839742 | GATACCAAGTGTGCT[C/G]CTGAAGAATGTGGTA | 405 |
rs587652834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872624 | ATCTCCTCCCAACTG[C/T]TCCCTCAGCCAATGC | 405 |
rs587652965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826246 | TTCACAGCATCTACA[A/G]AGGTTGGGCGCATGA | 405 |
rs587653075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150850774 | GGAGCCCCTCTGCCC[A/G]GCTGCCCAGTCTGGG | 405 |
rs587653124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826258 | ACAGAGGTTGGGCGC[A/G]TGAGCCACCATGCCT | 405 |
rs587653280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871722 | CAAGACCAGCCTGGC[C/T]AACATGGAGAAACCC | 405 |
rs587653358 | snp | C/G | 0.000289413 | 0.0120259 | intron-variant | ARNT | GRCh38.p7 | 1:150823395 | AGAAAATTTTCATTA[C/G]AAAAATAAATAAAAA | 405 |
rs587653454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865037 | AACAAGATGAAAATA[A/T]AAATTAAAATTAATC | 405 |
rs587653558 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARNT | GRCh38.p7 | 1:150827362 | CTCCCCAGCCAACCA[C/T]AAATCTGCTTTCTGC | 405 |
rs587653911 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150872297 | ACATTGCATGAATTC[C/T]TATTTTCCCATATCT | 405 |
rs587654064 | in-del | -/CAA | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150859821 | CGAGACTAGCCTTTG[-/CAA]CAACACAGTGAAACC | 405 |
rs587654358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867442 | TGTAGTCCAGCTACT[C/G]AGGTTGCTGAAGTGG | 405 |
rs587654406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843882 | CTTAACACATCATAT[A/G]AATGAATTCTGTTAT | 405 |
rs587654950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818798 | TAATTAAAATTAATC[A/G]TGGTAGGGAAAATGA | 405 |
rs587655092 | snp | C/T | 0.000600761 | 0.0173211 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836464 | AAACAGAAAGCCATC[C/T]GCTGCCTCCAAGATC | 405 |
rs587655137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854349 | GACTACTTGAACTCA[G/T]GAGTTTAAGACCAGC | 405 |
rs587655183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853370 | CAGTCAATCTTTGCC[A/G]GAGTTTTCAATCAGA | 405 |
rs587655280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835626 | GAAAAAAGGAGGAAA[A/G]CTAAAGATCAACAAC | 405 |
rs587655378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858244 | AGTAATCAAGTTGAA[A/G]TGAGATGGTCAGGAA | 405 |
rs587655583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874363 | TGAACATGGGATCAA[C/T]AAGTCAGAAGAGATG | 405 |
rs587655778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863006 | CAATGAGCCAAGATC[A/G]TGCCACTGCACTCTA | 405 |
rs587655965 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150815506 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGA | 405 |
rs587656096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846002 | TAATTTGTGCTCCTA[C/T]GGAAACCTTGCAAGC | 405 |
rs587656271 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811152 | AGATCTTCCAGATAA[A/G]GTGAGAGCACCAAAA | 405 |
rs587656312 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150863335 | CACTCCAGCCTGGGC[A/G]ACAGAATGAGACTCT | 405 |
rs587656341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838395 | GAAAACCATTTGTCT[C/T]ACCATTCTTTCTATT | 405 |
rs587656416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850341 | TGCCGAGCCGAAGCT[A/G]GACTGTACTGCTGCC | 405 |
rs587656586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827973 | TATTCTTCAGTCAAA[C/T]GTCAAGTCTTATGCT | 405 |
rs587656622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846076 | ATATACCGCCAGTTT[A/G]AAGCCATGTCACCTG | 405 |
rs587656765 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811396 | GACAAAGGTAAAATC[A/G]GGGACAAATTTTGCA | 405 |
rs587656770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150840555 | GGCCCATTAATGCAC[A/G]AAGTCCTACCTTCTT | 405 |
rs587656824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857913 | TTAATAAATACTTTT[A/G]GAGCTGAATGGACTC | 405 |
rs587657637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828841 | TTTGAATCATCTGTA[C/T]TAATATCAACAACAA | 405 |
rs587657651 | snp | A/G | 0.0101633 | 0.0705574 | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861265 | TAGTCCCAGCTACTC[A/G]GGGTCTGAGGCAGGA | 405 |
rs587657716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150835776 | ACTCTGGCCAAAAGA[C/T]TGAACATAATAAAAT | 405 |
rs587657895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846822 | TTACTTTCTGTGTCT[A/G]TGAATTTGACTACTT | 405 |
rs587658670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822579 | GGTCTGAAAGCTCTG[C/T]ACTCCTTCCTCCTTA | 405 |
rs587658759 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878719 | GCTGGGCTGGGCGGG[A/G]TGGCTGTAATCCCAG | 405 |
rs587658882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150831172 | CATCCAAAGTTTAAC[A/C]TTTTTCCAAAACACA | 405 |
rs587659166 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150850078 | CAAATAAATAGTCCA[C/T]TTTAAAAGCTCCAGA | 405 |
rs587659448 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876678 | CCAGAAGCGGCGCCT[C/G]ACCGCCGCCTCCGCT | 405 |
rs587659582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844080 | CATCAAGATACTGCC[A/G]ATAATAACTGATGGC | 405 |
rs587660089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867543 | AGAAAAAGAGAGAGA[G/T]ATCTTTTAAATAGAT | 405 |
rs587660138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821363 | TATTGCACTCAACAC[C/G]ATGAAAAATATGCAA | 405 |
rs587660223 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARNT | GRCh38.p7 | 1:150834150 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCAAACT | 405 |
rs587660308 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810245 | GAAGGAAAAGCAAAA[A/G]CAAAACCCCCAGAGC | 405 |
rs587660640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854455 | TAGCTACTTGGGTTG[A/G]GGGGGCGGGAGGGGC | 405 |
rs587660702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851044 | TGAGGAGCCCCTCCG[C/T]CCGGCAGCCGCCCCG | 405 |
rs587660832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865874 | TGTAAGAAATGCCTT[A/G]GATGTATGAAAATAT | 405 |
rs587661049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841245 | ATGAGCCACTGCGCC[C/T]GGCCTGCTTTATCTC | 405 |
rs587661131 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150821651 | GTTGTGATACATTTT[A/T]ATTTTTATTTTTTTT | 405 |
rs587661205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150874632 | GGTGGAGGCTGCCGT[A/G]AGCAGTGATCTTGCC | 405 |
rs587661341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871798 | CTGTAATCCCAGCTA[C/G]TCGGGAGGCTGAGGC | 405 |
rs587661398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817529 | ACAAATTAAACAGGC[C/T]GGGCATGGTGGCTCA | 405 |
rs587661485 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150837871 | TCTTAAAAAAAAAAA[A/C]CTGCCGTGCTCTTCC | 405 |
rs587661610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826389 | ATCCATAATTTCAAA[A/G]TATTAGTCCTTTTCT | 405 |
rs587661751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824603 | GGGACTAGAGGCGTG[A/C]ACCATCACGCCCAGC | 405 |
rs587661893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818237 | TGTTCTATGACACAG[A/G]GGTCATCTTGTTGGG | 405 |
rs587662139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150850307 | TCCCTCTCCCTCTCT[C/T]TCCACGGTCTCCCTC | 405 |
rs587662549 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150847105 | TCTCTTCAAGATTCT[G/T]CCTTCGATTATTTTG | 405 |
rs587662600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855516 | GCAGTGAGCCAAGAT[C/T]GCATCACCGCACTCC | 405 |
rs587662661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828609 | TCTTTTTCACCAACC[C/T]CTTTCACATAGCCAC | 405 |
rs587662750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857221 | GAAACATATTTGTCG[C/T]TTATAACTACATAGC | 405 |
rs587662842 | in-del | -/TG | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150852187 | CAGTATGTACTTCCT[-/TG]TGTAACCCCCTCACA | 405 |
rs587662919 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150863684 | AAATATAAAAAATTA[C/G]CAGGCGCCTGTAATC | 405 |
rs587663261 | snp | C/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150850430 | GCGATTGCAGTCGCG[C/T]GCCGCCACGCCTGAC | 405 |
rs587663285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870894 | AAAATGGGCCTCAGA[A/G]GGTGGCTCACACCTG | 405 |
rs587663355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838718 | CAATGATCATGTTAT[C/T]TTAATAACCAAAACA | 405 |
rs587664083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841751 | GTCTCACCACATAGG[C/T]CCATATTTAGTTACA | 405 |
rs587664203 | in-del | -/T | 0.124491 | 0.216211 | intron-variant | ARNT | GRCh38.p7 | 1:150851021 | GGCAGCCACCCCGTC[-/T]TGAGAAGTGAGGAGC | 405 |
rs587664378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851274 | GCCGCCGCCCCGTCC[C/G]GGAGGTGGGGGGCGC | 405 |
rs587664884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860684 | AACATGGTGAAATCC[C/T]ATCTCTACTAAAAAT | 405 |
rs587665083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150824804 | TCCATAAATAAAATT[A/G]AGTTGGCTTTAGTCT | 405 |
rs587665186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150853558 | TGACTTAATACCTAC[A/G]AAGATTGTTAGATAA | 405 |
rs587665741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845626 | AAAATAAAATAGGCC[A/G]GGTGCGGTGGCTCAC | 405 |
rs587665774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871995 | AGGGTCTCACTCCAA[C/T]ACCCAGGCTGGAGTA | 405 |
rs587665796 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811680 | CATACTATCCAAGGC[A/G]AACAGTGGATGTCAG | 405 |
rs587665802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873642 | AGGATTAACTTGGCC[A/G]GGTCAGTGGCTCACA | 405 |
rs587666946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150824121 | GCTAGGATTACAGGC[A/G]TGAGCCACTGAGCCC | 405 |
rs587667095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830158 | GAGGACCAGCCTGGC[C/T]GACACAGTGAAACCC | 405 |
rs587667136 | snp | A/G | 1.65386e-05 | 0.00287559 | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150852809 | ATCAAAATCCAGCCT[A/G]AGGAAAGCCAACAAT | 405 |
rs587667166 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811520 | CACATGTTTCTTTCC[A/G]GAGGGACTGCTCACA | 405 |
rs587667567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856340 | AGCTACTCGGGAGGC[C/T]GAGACAGGAGAATGG | 405 |
rs587667682 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150852563 | AGGGTTTGTAAATGC[C/T]GTCCTCTCCTCACTG | 405 |
rs587667741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868993 | TTAGCTGGGCATGAT[A/G]GTGCATACCTATGGT | 405 |
rs587667866 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817484 | AAAAAAAATTTTTTT[A/G/T]AAAAAAGAATCTGGA | 405 |
rs587667949 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150847250 | ACTCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 405 |
rs587668085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150855556 | AACAAAGCGAGACTC[C/T]GTCTCAAAAAAAAAT | 405 |
rs587668426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150813411 | TAATGCCACAAGTAA[A/G]CAACTATAGGTAAGC | 405 |
rs587668428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819201 | GGTGGTAACCTGACA[A/C]TTGATACCTACTAGA | 405 |
rs587668650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150820319 | TTGATACATAGAATT[A/G]AAACTAAACCCTTCC | 405 |
rs587669048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828446 | ACCTTTGCTGAAAAT[C/T]AGTTGACAAGTATAA | 405 |
rs587669195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864030 | ACACACCTAGGTATG[G/T]AGGTGTATAGCCTAC | 405 |
rs587669659 | in-del | -/AAAAAAC | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150840244 | AGACTCCATTTCAAA[-/AAAAAAC]AAAAAACAAAAAACA | 405 |
rs587669786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813453 | CCTAGGATAACTCTG[C/T]CCTTCTCTCTGCCAA | 405 |
rs587669916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850927 | GGAGCGCCTCTGCCC[A/G]GCCACGACCCCGTCT | 405 |
rs587670365 | snp | A/C/G | 0.000116543 | 0.00763282 | missense | ARNT | GRCh38.p7 | 1:150816807 | AATTCTCTGCCGGCC[A/C/G]GGGGGTAGGAGGGAA | 405 |
rs587670401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872814 | AAAAAAATTTAAAAT[C/T]AGCCAGCCACGGTGG | 405 |
rs587670618 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877980 | GTGCAGATTTATTTT[A/C]TTTTTTCTTTATTTT | 405 |
rs587670824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150852048 | ACTCCGTCTCAAAAA[A/C]AAAAAAAACAAAAAC | 405 |
rs587670895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856191 | CGTGCCTGTAATCCC[A/G]CACTTCGGGAGGCCA | 405 |
rs587671128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864357 | AAGACCTATTGGAAC[A/C]AACCCAAATGTCCAA | 405 |
rs587671326 | in-del | -/GGTC | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150866275 | GGCGTGAGCCACCAA[-/GGTC]AGTCAGCCTGTTCCA | 405 |
rs587671656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857167 | AAATACTATAATACT[A/G]TAACCTTTCTTAATA | 405 |
rs587671679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833388 | ATCCAGCTACTCAGG[A/G]AACTGAGGCATGAGA | 405 |
rs587671765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870798 | ACAGGTATGAGCCAC[A/C]ATGTCCAGCCCTAAG | 405 |
rs587671962 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150853733 | AGTGTCACATAAGGG[G/T]TACAATCAACATGCT | 405 |
rs587672376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839380 | TCTTGTCCAAAAAAC[A/G]AAAACTTTCAAGAGA | 405 |
rs587672502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867067 | AAAAAATTAGCCAGG[C/T]GTGGTGGCACACTGT | 405 |
rs587672597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823450 | ACTCTTGTCATTGTC[C/T]TTGAGGCACCAATAT | 405 |
rs587672761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150855460 | CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 405 |
rs587672768 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878640 | TTCATTTTTCTTTCA[C/T]TTTGTTGTTATATTT | 405 |
rs587672877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821294 | TTCTTGGGAAGACTT[C/T]CAGCATCACTAGTGG | 405 |
rs587672976 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150845858 | AGTGAGCCGAGATGG[C/T]GCCATTGCACTCCAG | 405 |
rs587673069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833301 | TTGAGGTCAAGAGTT[C/T]GAGGCCAGCCTGGCC | 405 |
rs587673482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860583 | AAGAGTGGCCAGGCA[C/T]GGTGGCTCACACCTG | 405 |
rs587673591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825707 | TACAAAAATTAGCTG[A/G]GCGTGGCAGCATGTG | 405 |
rs587673655 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150855141 | ATAATATGAAATAGG[-/A]AAAAAAAGTTTAGGT | 405 |
rs587673867 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150851624 | GGATTAAGGGCGGTG[A/C]AAGATGTGCTTTGTT | 405 |
rs587673938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874486 | ACCAGGAGATCAAGA[C/T]CAGCATGGGCAACAT | 405 |
rs587674070 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150841120 | CGCCCAGTTTTTTTT[A/T]TTTTTATTTTTAGTA | 405 |
rs587674122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150812450 | GACCTGTTTTGCTTT[C/T]TTTCAATCTTTGCTT | 405 |
rs587674375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862156 | CAGTTACATAGTACT[C/G]TGTACTATAAATGTA | 405 |
rs587674422 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150869874 | TACTGTTCTAGCTCC[-/T]TTTTTTTAGCACCTT | 405 |
rs587674449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843155 | TATTAACTTTGATTC[A/G]GTCCTTTTGCCATTT | 405 |
rs587674533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150848283 | CAACATGGCGAAACC[C/T]TGTCGCTACTAAAAG | 405 |
rs587675016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822131 | AATATATCCAGGCTA[C/T]GTAGCTTATTTTTGG | 405 |
rs587675120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860458 | TGACCTCAAGTGATC[C/T]GCCCACCTCAGCCTC | 405 |
rs587675570 | snp | A/C | 0.000627943 | 0.0177081 | intron-variant | ARNT | GRCh38.p7 | 1:150861226 | AAAATTAAAAATAAA[A/C]CTGGGTGCAGTGGTG | 405 |
rs587675854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848939 | CCGGGTGTGGTGGCT[C/G]ATGCCTATAATCCCA | 405 |
rs587676009 | snp | A/G/T | 3.29474e-05 | 0.00405867 | missense | ARNT | GRCh38.p7 | 1:150832385 | GAAACTGGGTCCACA[A/G/T]AGCTACTGCCACACC | 405 |
rs587676236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850473 | TTTTTTGGTGGAGAC[A/G]GGGTTTCGCTGGGTT | 405 |
rs587676807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150859744 | GCTGGGCACAGTGGC[A/G]GATGCCTGGAATCCT | 405 |
rs587676960 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150813812 | ACCACACCCGGTAGA[G/T]ACAGGGTTTCTCCAT | 405 |
rs587677239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150814371 | CTTATTTCCTATTGT[A/G]TATTTCTTCCAATTA | 405 |
rs587677509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837916 | CATCCTCCTAAGCTA[A/G]AAGCCTCAAAATCTA | 405 |
rs587678287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856309 | GTCGGGCATCATGGC[G/T]GGCGCCTGTAGTCCC | 405 |
rs587678428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862877 | CCAATATGGTGAAAC[C/T]CCGTGTCTACTAAAA | 405 |
rs587678437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816605 | ATGGAGCCTAGAACA[C/T]GGCAATAGGACAGGT | 405 |
rs587678546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150871463 | CTGCCACCATGCCTG[A/G]CTAATTTTTGTATTT | 405 |
rs587678595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150825554 | ACTCTCACTCATCCA[C/T]AAAAGAACAGTCTAG | 405 |
rs587679079 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150829314 | GTCTTTTGCATAGAC[-/ATA]AGATTCCCAGTTTTA | 405 |
rs587679347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828964 | ATAATGTTAGGTACT[A/G]ACAGAATATGATGAT | 405 |
rs587679377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846401 | GGTGAAAATATTCAA[C/T]AGAAAAAAAGCCAAT | 405 |
rs587679522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822483 | AATGAAATTTCCATT[A/T]AAACCCAAAAGGACT | 405 |
rs587679626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150834900 | AGTGGAAAGTAGTAG[C/T]AGAAAACAAGAGGCA | 405 |
rs587679724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830263 | AGGTGAGAGAATCAC[C/T]TGAACCCAGGAGGCG | 405 |
rs587680223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838928 | TCACATACTTATATT[C/G]AGATGAAGTTCCTGA | 405 |
rs587680262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835547 | TTCAAGATTACAGTA[A/C]GCTATGATGTGCCAC | 405 |
rs587680297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864177 | TAAACATAGAAAAAG[C/T]AATGTGTTGTGCTAA | 405 |
rs587680401 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811752 | TATACAATTTCAGGT[A/C]AGGAGACATAAGGAA | 405 |
rs587680757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848156 | ACAAACTGGAAACTG[C/T]AGTTGTCTAAAGAGT | 405 |
rs587680973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860376 | ACGCACCACCACGCC[C/T]GGCTAATTTTTGTAT | 405 |
rs587681199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847551 | GGAAAAGGACAAACG[A/G]ACCTCTCTTTGGATC | 405 |
rs587681266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825345 | AATCTTCCCAACAAC[C/T]GTCTGAATTTAGGTA | 405 |
rs587681358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830619 | ACATCCATTCTATGA[C/G]CATGTTATAGGCAGA | 405 |
rs587681462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868212 | GTAATCCCAGCTACT[C/T]AGGAAGCAGAGGTGG | 405 |
rs587681673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821521 | ATTATTACAACAGTA[C/T]AGTATATACTATAGT | 405 |
rs587682192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150833065 | TAAAGTCAGTATTAA[C/T]ATTATCGCCAATGTG | 405 |
rs587682211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866437 | CATAATGGGCCTTGA[C/T]GTGTGCACAGCCCCT | 405 |
rs587682270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826803 | GGGTGTGCTACCACA[A/C]CTGGCTAATTTTGTA | 405 |
rs587682293 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150845195 | GAAGCTGAGGTAGGA[-/G]GATCACTGAAACCCC | 405 |
rs587682322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855827 | GGATTGCTTCCTGGG[C/T]CCAAGAAGTTGAGGC | 405 |
rs587682464 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809469 | CAAAAATTAGCTGGG[C/T]ATGGTGGCACACACC | 405 |
rs587682546 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150835873 | ATACATTGACCAATA[A/T]CCATATCTATAGAAT | 405 |
rs587682914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819521 | AACAACCAAATGTCC[A/G]TTAACGAACATACAG | 405 |
rs587683120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839159 | TGGTTCCATGGACAT[A/C]GTCATTTCCTCTGTG | 405 |
rs587683141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816979 | CTCAGGTGGTATTAT[A/G]ATTAAGTGGAAAAAC | 405 |
rs587683289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872963 | CAAGACCCTCTCCTA[C/T]GGGGAAAAAAAATGT | 405 |
rs587683334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833971 | CAGAGTTTCACTCTT[G/T]TTGCCTAGGCTGGAG | 405 |
rs587683422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874847 | TCTGCACACACACAT[A/T]CACACTAACATATGC | 405 |
rs587683434 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150873790 | CCAGGTGTGGTGGTG[C/T]GTGTCTGTAGACCCA | 405 |
rs587683449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150823903 | GCTAGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 405 |
rs587683822 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150843708 | CCAAAGTGCTGGAAT[A/T]ACAGGCATAAGCCAC | 405 |
rs587684059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862254 | GCACAGGTGCCAGTA[C/G]TTCCATATTATTTCT | 405 |
rs587684475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150844209 | TATTTCAATTAGTTT[C/T]GATAAACAAATTATT | 405 |
rs587684504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150820521 | AATTAGCCAGGCGTC[C/T]TGGTAGATGTCTGTA | 405 |
rs587684639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850538 | ATCCGCCAGCCTCGG[A/C]CTCCCGAGGTGCCGG | 405 |
rs587684965 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150828041 | ATATTCCTGGTACAA[A/G]TCCTCTTTCAGGTAT | 405 |
rs587685430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823644 | CAACCACCACCCCTC[A/G]GGTTCAAGCGATTTT | 405 |
rs587685488 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150813640 | ATGTGGGTAGTTTTT[A/T]TTTTTTATTTTTTAT | 405 |
rs587685583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150859211 | ACCTAAATTCCAATA[A/C]TTAAAAGAAAATTAT | 405 |
rs587685690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848329 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 405 |
rs587685702 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARNT | GRCh38.p7 | 1:150851103 | GCAGCCGCCCCGTCC[A/G]GGAAGTGAGGAGCAT | 405 |
rs587685718 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150824205 | TGCCATTTAAAAAAA[C/T]GGCAAAAAATCACAA | 405 |
rs587685730 | snp | C/T | 1.65326e-05 | 0.00287507 | intron-variant | ARNT | GRCh38.p7 | 1:150816924 | TGGGGAAGGGCCAGT[C/T]AAGGGGCTGTAGTAT | 405 |
rs587686312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865415 | TGACAAGGGAAAAAG[C/G]AGAAAACCAACTCAA | 405 |
rs587686329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839693 | CCATCCAGGTGGTCA[C/T]ATCTGGTCATTTGGT | 405 |
rs587686450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817606 | TGAGGTCAGGAGTTC[A/G]ACACCAGCCTGGCCA | 405 |
rs587686887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812615 | GAACACTTCATGAAT[C/T]TGTGTGTCATCCTTA | 405 |
rs587687195 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150851087 | GGAGCCCCTCCGCCC[C/T]GCAGCCGCCCCGTCC | 405 |
rs587687301 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877089 | CCAACATGGCGAAAC[C/T]CCGTCTCTACTAAAA | 405 |
rs587687316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821087 | TGTTATTAAGAAAAT[C/T]ATAAGGAAGAGAAAA | 405 |
rs587687377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150814242 | GGGTAGCCACCTGCT[A/G]AAGAGAGATGGAGAG | 405 |
rs587687418 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150868703 | TCAGGAGATCGAGAC[C/T]ATCCTGGCCAACATG | 405 |
rs587687521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849305 | TTATCAAATTGTCTG[G/T]TACTCAGCAACGTAC | 405 |
rs587687688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839823 | CCTTCTCATGCAAAG[C/T]AAGCATGAAACAGAA | 405 |
rs587688002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870445 | CACTGCAATGCTCTG[A/G]TAAACAAGGAAAGCA | 405 |
rs587688313 | snp | A/G | 0.48155 | 0.0942576 | intron-variant | ARNT | GRCh38.p7 | 1:150831925 | GAGTTACAGGAGTTT[A/G]AAAAAAAAAAAAAAA | 405 |
rs587688606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848883 | CCCAATTAAAGAAAA[A/C]ACTTAGTTAACAAAA | 405 |
rs587688790 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARNT | GRCh38.p7 | 1:150851006 | AGGAGCCCCTCTGCC[C/T]GGCAGCCACCCCGTC | 405 |
rs587689241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150846886 | ATTGTCTTTTTGTTA[C/T]TGGCTTATTCTTTCA | 405 |
rs587689736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869659 | CAGAGATCCTCCCAC[A/C]ACCTCAGCCTCCCAA | 405 |
rs587689782 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARNT | GRCh38.p7 | 1:150851667 | GAAGGCAGCATGCGC[A/G]TTAAGAGTCATCACC | 405 |
rs587689877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812871 | TCATACTCCTTTTTT[C/G]TTTGTTTGACAGGGA | 405 |
rs587690024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863229 | TAGTCAGGTGTGGTG[A/G]TACACGTCTATAATC | 405 |
rs587690100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841542 | TGACCCAGATTAAAG[A/G]GGAAATAGTAGAAAA | 405 |
rs587690729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836782 | CACAGCGGCTCCCGC[C/T]GGTAATCCCAGCACT | 405 |
rs587690982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150854685 | AACATGGTGAAACCT[C/T]GTCTCTACTAAAAAT | 405 |
rs587691222 | snp | A/G | 9.88566e-05 | 0.00702983 | intron-variant | ARNT | GRCh38.p7 | 1:150816248 | GGGAACACACAGATG[A/G]TAAGTTTTACCTGGG | 405 |
rs587691273 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150866344 | AAGACCAATCTGATA[C/T]CTGAATCTTTTGAAT | 405 |
rs587691328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843604 | AGTTTAGAGTTTTAC[A/G]TTCCTTGGGTTATTT | 405 |
rs587691362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856006 | AGGTGAAAAGACTAG[A/G]CCATGTAAAACTATA | 405 |
rs587691473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818542 | GGATTGCTTGAGCTC[A/G]GGAGTTTGAGACCAG | 405 |
rs587691539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837211 | AAGTTTTCTCAATTC[C/T]AGATAAATCTTCCCT | 405 |
rs587691786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844708 | ACTGACATTTAAGAA[C/T]TTAATAAAAAAAAGT | 405 |
rs587691891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150867259 | ATAGAGCTGGGCATC[A/G]TGTCATACACCTATA | 405 |
rs587691901 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809957 | ATGATTTCTGATTCC[G/T]GAAATTAAAGACACA | 405 |
rs587691949 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150854926 | AGGTAATTGCTAAGT[A/C]AAAGGAAAAAAATGA | 405 |
rs587692060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855650 | GTCATGTCTGTAATC[C/T]CAACACTTTAGGACG | 405 |
rs587692343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150876479 | CCTCAGCCCTGGGTC[C/T]CCTTAGTTGTCAGCC | 405 |
rs587692377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821948 | ACTTGGTATCCCAAA[C/G]TGATAAAGTGATGGG | 405 |
rs587692504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850746 | GCCTGGCCGCCCATC[A/G]TCTGGGATGTGAGGA | 405 |
rs587692612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150871085 | GAAGAGTTTATGTGA[A/G]AAGTTGGAGACAGTT | 405 |
rs587692991 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877717 | AACCTCCACCTCCCC[A/G]GTTCAAGCAATTCCC | 405 |
rs587693022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150831413 | AAAGTCTTTGCAGAG[A/T]ATATCCTCTTGATAA | 405 |
rs587693121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857468 | CTGTAAAGCTACTGA[A/G]CATATAACAAGTCTT | 405 |
rs587693291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872559 | CTACACTTACTACAA[A/T]CTCATTCAACATCTC | 405 |
rs587693607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860761 | CTCGGGAAGCTGAGG[C/T]AGGGAGAATTAATTG | 405 |
rs587693704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858768 | CTAGGACTATAGGCC[C/T]GCACTACCACACCCA | 405 |
rs587693756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824199 | ATTTTTTGCCATTTA[A/T]AAAAATGGCAAAAAA | 405 |
rs587694027 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150860326 | GTTCAAGTGATTCTC[C/G]AGCCTCAGCCTCCCA | 405 |
rs587694435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150815634 | GGAGGCTGAGGTGGG[C/T]GGATCACAAGGTCAG | 405 |
rs587694624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846477 | AACTTAAAAGACCCA[C/T]AACTATTATTTGTCA | 405 |
rs587695371 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810043 | GTGCCTGTTGTTTAT[C/G]AACTGGAAAGGAATG | 405 |
rs587695555 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARNT | GRCh38.p7 | 1:150850680 | CCCAAAGTGCCAGGA[C/T]TGCAGCCTCTGCCTG | 405 |
rs587695675 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150813397 | ATTCCATTGTGTACT[-/A]ATGCCACAAGTAAAC | 405 |
rs587696316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827768 | CTTTTGCAAAGCTAG[C/T]AGCTATACCATTTTA | 405 |
rs587696354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824257 | ACTATTCTAGTCAAA[C/T]AGGAATAATAACTTA | 405 |
rs587696396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873050 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 405 |
rs587696552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813680 | ACGGAGTTTCACTCT[C/T]GTTGCCCAGGCTGGA | 405 |
rs587696791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841027 | GATCTCGGCTCACTG[A/C]AACCTCCGCCTTCTG | 405 |
rs587696934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824077 | CGATTTCCCGACCTC[A/G]GGATCCGCCTGCCTC | 405 |
rs587697150 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876788 | GGCGGAGTCAACACA[A/C]GGCCAGCCTCCTAAG | 405 |
rs587697267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869377 | AGCTACTCGCGAGGA[C/T]GAGGCAGGAGAATGG | 405 |
rs587697277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855248 | AAGTACATCCTTTCA[C/T]GCAACCATTAAAAAT | 405 |
rs587697329 | in-del | -/A | 0.49949 | 0.0159663 | intron-variant | ARNT | GRCh38.p7 | 1:150847425 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 405 |
rs587697384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817680 | CGGGGGTGGTGGCAG[A/G]CACCTGTAATCCCAG | 405 |
rs587697517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858732 | GCTCAAGCAATCCTC[C/T]CACCTCAGCTTCTGG | 405 |
rs587697593 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811956 | TTCTGTTTACAGAAA[C/G]ATTTGCTTTTTAAAA | 405 |
rs587697635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863304 | AAGGCTGCAGTGAGC[C/T]GAGATCATGCCACTG | 405 |
rs587698039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862329 | GATTGCCCATTACCT[A/G]CCAAGGAGGTTATAC | 405 |
rs587698301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150834095 | CACGCCACCACGCCC[A/G]TCTAATTTTGTTGTT | 405 |
rs587698855 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150823557 | GAGACTTAAGCTTTT[G/T]TTTTTTTTTTTGAGA | 405 |
rs587698962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150872875 | GCTGAAGTGGGAGGA[C/T]CACATGCTCCCAGAA | 405 |
rs587699266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873469 | AAAAATCATCACAGA[A/G]CTATTACTTCAACAC | 405 |
rs587699355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150868177 | TTCTAGCCCCAAGCC[A/G]GGCACTGTGGTGTAC | 405 |
rs587699643 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150834361 | CTATCATAGTGTCTG[C/G]CAAGTTCAGAAACGT | 405 |
rs587699922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819886 | ATATACTAAAAAACA[A/C]TGTATACTTTAAATG | 405 |
rs587700006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863158 | CACTTAAGGTCAAGT[C/T]TGAGACCAGCCTGAC | 405 |
rs587700152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837003 | CCTGGGAAGCAGAGG[C/T]TGCAGTGAGCCGAGA | 405 |
rs587700750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847505 | AACCCGACTTGGTAA[G/T]ATAAACTACGATAGT | 405 |
rs587701112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816072 | GAAAACCACAGACTC[C/T]ACTGAGATTTTTTTT | 405 |
rs587701251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150853111 | CATGCTGAAACCCCA[C/T]CTCTACTAAAAATAC | 405 |
rs587701484 | snp | C/T | 8.75618e-05 | 0.00661614 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817995 | GGCCTCTGGATTGTG[C/T]TGGAGAGTGTAGGCC | 405 |
rs587701838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150827885 | TATAGTGGTATCTCA[C/T]TGTGATTTTAATTTG | 405 |
rs587702027 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877178 | GAGGCAGGAGAATCG[C/T]TTGAACCTGGGAGGC | 405 |
rs587702673 | snp | C/T | 0.000170913 | 0.00924268 | intron-variant | ARNT | GRCh38.p7 | 1:150852889 | CTCAACACAAGCTAC[C/T]GGAACACCCACCCAA | 405 |
rs587702726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861013 | ATGTAAAGTGCTCAA[C/T]ATAACCAATCGCTAG | 405 |
rs587703184 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150817732 | GTGAATCACTTGAAC[C/T]CAGGAGACAGAGGTC | 405 |
rs587703485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812512 | TTACTCCATTCACTC[C/T]TGCAGTCCCTCAGGA | 405 |
rs587703822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843941 | CTATTTCTACTACTA[C/T]TACTACTACAGATCC | 405 |
rs587704176 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878121 | CTGAGTAGCTGGGAT[C/T]ACAGGCGCGCACCAC | 405 |
rs587704266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857194 | AATAGATTGTGAACA[A/T]CTTTCTACACTGAAA | 405 |
rs587704303 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150850422 | GAGTGCCTGCGATTG[C/T]AGTCGCGCGCCGCCA | 405 |
rs587704323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150875677 | AGAGGGCTGGGACTA[A/G]TAATTTGAAGATCTG | 405 |
rs587704498 | snp | A/G | 0.000399281 | 0.0141238 | missense | ARNT | GRCh38.p7 | 1:150813179 | TCTCTTACCTGGAAG[A/G]CCTCAGGCTGGCCAG | 405 |
rs587704532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150867616 | ATTTTTGGAGTCTTT[C/T]ATACATAAAAGATAA | 405 |
rs587704545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865745 | TGTATGCATACTACA[C/T]GCTTCATTTTTCTTC | 405 |
rs587704571 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150840007 | GCACTTTGGGAGATG[C/G]AGGCAGGTGGATTAC | 405 |
rs587705013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868628 | CTGGGCAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 405 |
rs587705123 | snp | A/C | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810072 | TGATAAAGCCGCAAT[A/C]AAGATCACACAACAC | 405 |
rs587705249 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150843573 | ACAAGAGAAGGAGAA[A/C]TGAGTGATATTCAGC | 405 |
rs587705401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854108 | TTTCTTTTTAAGAGA[C/T]AAGCTCTCACTCTGT | 405 |
rs587706206 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858150 | AAAAAGAACTGCTTA[C/T]GGGAAACTTGGATAA | 405 |
rs587706334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823076 | CACATGCCACCACGC[C/G]CGGCTAAATTTTTGT | 405 |
rs587706580 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150837378 | TGTTTGGTTTGGTTT[C/T]TGTTCTGCCAGGAAC | 405 |
rs587706793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863627 | TAAGGTCAGGAGTTC[C/G]AGACCAGCCTGACCA | 405 |
rs587706826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842228 | AAATCCCTAAGCAAA[C/G]TTCCCTCAACTCACC | 405 |
rs587707067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830500 | TATTTACATATATAT[G/T]AATTCCTACATTTTA | 405 |
rs587707082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867949 | TCCCATACAGCCTGC[A/G]GAACTATGAGTCAAT | 405 |
rs587707138 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150835171 | TAAAAAGAAAAAATT[G/T]TAAAAAGAAAAAAAC | 405 |
rs587707193 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876904 | GAAGTCCAGCTGTCT[C/T]CCTAATCTCGCCCTC | 405 |
rs587707304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857709 | TTTACCAACAAATGC[A/C]TATTTCCATACACAG | 405 |
rs587708029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825709 | CAAAAATTAGCTGGG[C/T]GTGGCAGCATGTGCC | 405 |
rs587708407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871779 | CCGGCGTGATGGCAG[A/G]TGCCTGTAATCCCAG | 405 |
rs587708842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830086 | TTTATGGGCCAGGCA[C/T]CGTGGCTGACGCCTG | 405 |
rs587708857 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150850974 | CTCCGCCCGGCAGCC[A/G]CCCCGTCTGAGAATT | 405 |
rs587708910 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877294 | ATATTTTACTAAAAA[C/T]CTTCGCTTGGTGGTG | 405 |
rs587708994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815586 | ATTTTTCAGCCAGGC[A/G]CGGTGGCTCACGCCT | 405 |
rs587709218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875257 | TTTACCTCCCTTTCC[G/T]TCAAAAAAAATTTAA | 405 |
rs587709240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856705 | GAGGTGGAGATTGCA[A/G]TGAGCCAAGATCACA | 405 |
rs587709407 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150870682 | TGCTAATTTTTTGTA[-/T]TTTTTTTGTACAGAT | 405 |
rs587709660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150851264 | CCTCCGCCCAGCCGC[C/T]GCCCCGTCCGGGAGG | 405 |
rs587709860 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150873309 | AAACAAACAAACAAA[A/C]AAAAAACAAAACAAA | 405 |
rs587710019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826255 | TCTACAGAGGTTGGG[C/T]GCATGAGCCACCATG | 405 |
rs587710123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150815819 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCTA | 405 |
rs587710214 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150872639 | TTCCCTCAGCCAATG[A/C]ATTACAAATGACACA | 405 |
rs587710418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819137 | ATAATCTGATCTTCA[A/G]GAGGTGGATTCAAGG | 405 |
rs587710481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818106 | AGAAAGAGAAGAATA[A/G]GATTCTGTATGTAAA | 405 |
rs587710531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841094 | GCTGGGACTACAGGC[A/G]CACACCACCACGCCC | 405 |
rs587710538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836546 | CTGAAAAAACAAGTA[C/T]TTCTATTCACAGGAA | 405 |
rs587710706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826936 | ACAGGTGTGAGCCAC[C/T]GTGCCCAGCCAACAT | 405 |
rs587710795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821400 | TGAGATTTCACTGTT[G/T]ACTGCAATATGCAAT | 405 |
rs587710835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849798 | GGCTGGACATGGTGG[C/T]TTATGCCTATAACCC | 405 |
rs587710976 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARNT | GRCh38.p7 | 1:150845247 | CTATGATCATGCCAC[C/T]GTACTCCAGCCTGGG | 405 |
rs587711156 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150849565 | CCAAGGTGGGAGGAT[G/T]GCTTGAGCACAGGAG | 405 |
rs587711339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150852020 | ACCACTGCACTCCTG[G/T]CGACAGAGCAAGACT | 405 |
rs587711352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872379 | AAAACTAAGTTATAT[A/C]GGTGAAAATTAGCTA | 405 |
rs587711395 | in-del | -/T | 0.000250842 | 0.0111963 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811982 | AAAAACAAACAGTGA[-/T]TTTTTTCTCCCCCAC | 405 |
rs587711469 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARNT | GRCh38.p7 | 1:150850288 | TCTCCCTCTCCCCAC[A/G]GTCTCCCTCTCCCTC | 405 |
rs587711662 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878728 | GGCGGGGTGGCTGTA[A/G]TCCCAGCACTTTGGG | 405 |
rs587711882 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150850392 | CCCTGCCTGATTCTC[C/T]TGCCTCAGCCTGCCG | 405 |
rs587712215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853489 | GAGTCTGCTCTAAGC[A/C]GTGTTACCAAATTTC | 405 |
rs587712294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835720 | TTAAATTTTTTTCTA[C/G]AGTTGCTCAAGAATA | 405 |
rs587712398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150868854 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 405 |
rs587713109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150814555 | AGTATTATATGCAGG[C/T]CAGGCGGGGTGGCTC | 405 |
rs587713118 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860835 | GCACTCCAGCCTGAG[A/C/T]GACAGAGAAAGACTC | 405 |
rs587713459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150829399 | ACAATCAGACAAGGC[A/C]TAAGGTCTAGCTCTG | 405 |
rs587713878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833256 | GGCCTGTAATCTCAG[C/T]ACTTTGGGAGGCTGA | 405 |
rs587713954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150828753 | GCATGTTTTATGGGC[C/T]ATTATTCATTTAGGT | 405 |
rs587714305 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150864536 | CAAACACCGCATATT[C/G]TCACTCATAGGTGGG | 405 |
rs587714761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830997 | GCACTGGGCTGGATG[C/T]TTTCCTTACATTAAA | 405 |
rs587714975 | in-del | -/CAT | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150833139 | GGTTTCAGAAGATAG[-/CAT]CAAAGCTAGAATTCA | 405 |
rs587715018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824634 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGTTT | 405 |
rs587715235 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811903 | GGGAAAGGGGGTACA[C/T]GTCAGGGGTGAGGGA | 405 |
rs587715334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835953 | GAAAAAATACCAGAT[A/G]ATTATCCATACAAAT | 405 |
rs587715449 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864252 | ATCTCCATTATAATC[A/T]TATGGGACCACCATC | 405 |
rs587715493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835249 | TTATTATACAGAAAC[A/G]AAGAACAACTTTTGG | 405 |
rs587715646 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150853473 | CCATGTTTCATTTCT[-/AG]AGTCTGCTCTAAGCC | 405 |
rs587715681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875498 | AAATTCTCCGCCCCA[C/G]GCAACACACACACAT | 405 |
rs587715765 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150852349 | ATTCAGTCTGGCCTC[A/C]TTGAGGATAAAAAAA | 405 |
rs587715785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863741 | AGAATTGCTTGAACC[C/T]AGGAGGCAGAGGTTG | 405 |
rs587715816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150868918 | ATAATAATAAAATTT[A/T]AAAAAAAAAGGACCA | 405 |
rs587716129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150856916 | TGGGCCATGATTGTG[C/T]CTCTGCACTCCAGCC | 405 |
rs587716236 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876660 | GAAAAGAAAGGCCAC[G/T]CCCCAGAAGCGGCGC | 405 |
rs587716640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839942 | CCTCAGAACAAAAGC[G/T]GTTTTAAGAAACGAC | 405 |
rs587716774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826190 | AGAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 405 |
rs587716918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872805 | CTGTCTCTAAAAAAA[A/G]TTTAAAATTAGCCAG | 405 |
rs587716961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150820212 | TCTAGCCCCACTTAT[A/G]GAAAGAGCTTGCCTA | 405 |
rs587717024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868098 | TAGGAAGGCAAGCAG[C/T]TAGAAAGGCAGGTAG | 405 |
rs587717067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150832203 | TAAGTGGGAGGTAAG[C/G]GATGTTAAGTGGGAG | 405 |
rs587717083 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878550 | TACTGCGCAGATTAC[A/G]TTGATCCACTTATTT | 405 |
rs587717841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150814827 | TAGCCTGGGCAACAG[C/T]GAGACTCTGTCTCAA | 405 |
rs587718021 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARNT | GRCh38.p7 | 1:150850899 | CTGCCCCGCCACCCC[A/G]TCTGGGAGGTGAGGA | 405 |
rs587718166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866848 | AAAGATACAGAAAGG[C/T]AGGAAGAACAGCAGA | 405 |
rs587718170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862100 | CCACGTAACAATATA[C/T]TGCTATGGCAATAAA | 405 |
rs587718240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815920 | AGACATCACTGTAAG[C/T]TAGTCATTAATTTTC | 405 |
rs587718559 | snp | A/C | 0.000101704 | 0.00713032 | intron-variant | ARNT | GRCh38.p7 | 1:150816420 | TCCTAGGAGTGAATA[A/C]ATGAGGTAAAAGATT | 405 |
rs587718738 | in-del | -/CACAATGTGC | 0.00993419 | 0.0697739 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809969 | TCCTGAAATTAAAGA[-/CACAATGTGC]CTTATGTTTGTATGT | 405 |
rs587718781 | snp | A/G | 0.00083022 | 0.0203573 | intron-variant | ARNT | GRCh38.p7 | 1:150853277 | CAACTGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 405 |
rs587718796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850433 | ATTGCAGTCGCGCGC[C/T]GCCACGCCTGACTGG | 405 |
rs587719071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823425 | ATTTTCCAATTTCTA[C/T]AACCCTAAAACTCTT | 405 |
rs587719145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858252 | AGTTGAAGTGAGATG[C/G]TCAGGAATAGCGAAG | 405 |
rs587719374 | snp | C/T | 1.67562e-05 | 0.00289444 | intron-variant | ARNT | GRCh38.p7 | 1:150831809 | ATATTTACTATTTCA[C/T]TTTCTTACCTGCTGG | 405 |
rs587719582 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150850330 | TCTCCCTCTGATGCC[A/G]AGCCGAAGCTGGACT | 405 |
rs587719879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819210 | CTGACAATTGATACC[C/T]ACTAGATGGCTACAA | 405 |
rs587720091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874197 | AAGCACAGTACATTT[C/T]CACCTATGTCCCTCC | 405 |
rs587720614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150861889 | TACTTTATTATAAAG[C/T]AGAATTTAAGTTAGA | 405 |
rs587720815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856259 | CCTGGCTAACACGGT[C/G]AAACCCCGTCTCTAC | 405 |
rs587720879 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150851280 | CCCCGTCCGGGAGGT[-/G]GGGGGGCGCCTCTGC | 405 |
rs587721229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851178 | CGCCTGGCCAGCCAC[C/G]CCGTCCAGGAGAGAG | 405 |
rs587721300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842605 | AAAGGAGAAAGAAGA[A/G]AGAAAAGGATATAGA | 405 |
rs587721425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150876140 | CCAGGGTTTATGAAT[C/G]CAAACTACTCTTAAA | 405 |
rs587721609 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150826039 | GTGCCTCAGCCTCCC[A/G]AGTACCTGGGATTAC | 405 |
rs587721819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864778 | AAAAAATAAATAAAT[A/T]AATAAATAAATAAAT | 405 |
rs587722152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836038 | TTGGCTTTTACTGTT[C/G]TATTTATACCAATAT | 405 |
rs587723011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871681 | TTGGGAGGCCAAGGT[C/G]GGCGGATCACCTGAG | 405 |
rs587723588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150872234 | AAGGGATTAGAGGCA[C/T]GAGCCACCACACCTG | 405 |
rs587723702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838977 | GCCTTCTTTTTTTCA[C/T]AGTGATCACATGTAA | 405 |
rs587723887 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150844505 | ATCTCTCTACATCAA[A/C]GGTTCTTAAAGTATG | 405 |
rs587723935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862984 | TGAACACAAAAGGCG[A/G]AGGTTGCAATGAGCC | 405 |
rs587723985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815301 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 405 |
rs587724394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150847029 | TGTCAGTGGACATTT[C/T]GGTTACTTCGACCTC | 405 |
rs587724502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830165 | AGCCTGGCCGACACA[C/G]TGAAACCCCATCTCT | 405 |
rs587724857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150816024 | AATCAGACGTGCTCA[A/G]AACGTTCCAAGTGAG | 405 |
rs587725035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150822407 | ACCTCATGGAGGGGA[A/G]CCGGTACCTAAGGTT | 405 |
rs587725251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150873445 | ATGAAGAATTATCAA[C/T]TCGAGAAAAAAAATC | 405 |
rs587725599 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150820349 | CATCTCAGGACCTAG[A/T]CTCTGAATTATTGTT | 405 |
rs587726005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846545 | AAAAAAAGATGATGA[C/T]CTAATGACAACACAG | 405 |
rs587726709 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150853589 | TGTTTCTTTCCTTCA[C/T]TGATCTAATAAACAT | 405 |
rs587726728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150843773 | CAGGACTAACCAGGC[A/G]TGGTGGCTATGCATA | 405 |
rs587726887 | snp | A/T | 0.0225045 | 0.103662 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809609 | GCGAGACTCCATCTC[A/T]CACACACACACACAC | 405 |
rs587726946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847302 | TGGGTGTGGTGGCAC[A/G]TGCTTATAGTCCCAG | 405 |
rs587727207 | snp | A/G | 5.05421e-05 | 0.00502678 | intron-variant | ARNT | GRCh38.p7 | 1:150814276 | ATATAGAACAAATAC[A/G]GCATTAACATCATTG | 405 |
rs587727404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150852146 | GTCACAGATTAATGA[C/T]ACCTCAACCAATGAA | 405 |
rs587727489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870681 | CCTGCTAATTTTTTG[C/T]ATTTTTTTGTACAGA | 405 |
rs587727501 | snp | A/G | 0.162909 | 0.23434 | intron-variant | ARNT | GRCh38.p7 | 1:150851347 | CCCGGCCGCCACCCC[A/G]TCTGGGAGGTGTACC | 405 |
rs587727835 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150856203 | CCCGCACTTCGGGAG[A/G]CCAAGGCGGGTGGAT | 405 |
rs587728007 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150824426 | CCTATTTTTTCCCCG[-/A]AACCTGAGAACATCT | 405 |
rs587728018 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150854890 | AAAGGGAAGGGGAAA[A/G]AGAGGGAAGGAGGGA | 405 |
rs587728184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848959 | CTATAATCCCAGCAC[C/T]TTGGGAGGCCGAGGT | 405 |
rs587728225 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150850481 | TGGAGACGGGGTTTC[G/T]CTGGGTTGGCCGGGC | 405 |
rs587728639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874508 | GGGCAACATAGCAAG[G/T]CATCTGTCTCTACAA | 405 |
rs587728733 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150856371 | CGTGAACCTGGGAGG[G/T]GGAGGTTACAGTGAG | 405 |
rs587728769 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857103 | GAAATGTGGTATATA[-/T]TCTTTCAGTTTTTTC | 405 |
rs587729118 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150822812 | GCAGTCTTGTGGTAC[G/T]GCATACACAAATTGG | 405 |
rs587729230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150866346 | GACCAATCTGATACC[C/T]GAATCTTTTGAATGT | 405 |
rs587729363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869142 | TCAAAAAAACCCTTA[A/G]AAGTATTTAAAGAAT | 405 |
rs587729448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844163 | TTCTCATTTTAGAGA[C/T]GGTTCACATCCTAAA | 405 |
rs587729705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855494 | ATGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 405 |
rs587729717 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877763 | GAGTAGCTGGGATTA[C/T]AGGCGCACGCCACAC | 405 |
rs587729908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150867467 | AAGTGGGAGGAATGC[C/T]TGAGCCCAGGATTTC | 405 |
rs587729941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845759 | ATACAAAAATTAGCT[G/T]GGCGTGGTGGCAGGG | 405 |
rs587730033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150840223 | TTCAGCCTGGGTGGC[A/G]GAGCAAGACTCCATT | 405 |
rs587730502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824200 | TTTTTTGCCATTTAA[A/T]AAAATGGCAAAAAAT | 405 |
rs587730803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860362 | CTGGGATTACAGGCA[C/T]GCACCACCACGCCTG | 405 |
rs587730928 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150824751 | TGAGCCACTGCACCC[A/C]GATGAGAGCATCTGT | 405 |
rs587731074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150840354 | CTTGGTTAACTCCCA[G/T]GCTTACTAATTCAAC | 405 |
rs587731247 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811716 | TCTAACCTGCCTCTT[C/G]ATCTCAGCACAAATC | 405 |
rs587731340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835791 | CTGAACATAATAAAA[C/T]AGGGGAGAAAAAAAG | 405 |
rs587731865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873504 | CTTAGAGAGTACCAA[C/T]CATATTTTACTCTTC | 405 |
rs587731894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150859906 | CAGCTACTCAAGAGG[C/T]TGATGTGGGAGGATC | 405 |
rs587732140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150852984 | CCCAAACTAGGCAAA[A/G]AAGTACAAAACTGGG | 405 |
rs587732484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860286 | AGTGGCGCAATCTTG[C/G]CTCCCTGCAACCTCC | 405 |
rs587732507 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849940 | TGTGGTAGTCCCAGC[C/G/T]ACTCAGGAGGCTGAG | 405 |
rs587732683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873655 | CCGGGTCAGTGGCTC[A/G]CACCTATAATCCCAG | 405 |
rs587732745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860586 | AGTGGCCAGGCACGG[C/T]GGCTCACACCTGTAA | 405 |
rs587733085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825802 | TACAATGAGCTGAGA[C/T]TGCACACTACACTCC | 405 |
rs587733110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855557 | ACAAAGCGAGACTCC[A/G]TCTCAAAAAAAAATA | 405 |
rs587733247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813511 | GCCCTAAATTAATTC[G/T]TCTTCTCCAGGCAGC | 405 |
rs587733344 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150846415 | ATAGAAAAAAAGCCA[A/G]TGGAAAAGCATCACA | 405 |
rs587733526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874356 | ATTGAACTGAACATG[A/G]GATCAATAAGTCAGA | 405 |
rs587733705 | snp | C/T | 4.95372e-05 | 0.00497656 | missense | ARNT | GRCh38.p7 | 1:150813299 | ACACCCTCTGCTGTC[C/T]GTGTCTGGAATTGTC | 405 |
rs587733721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150871583 | TAGGATTACAGGCAT[A/G]AGCCACCATGCCCGG | 405 |
rs587733924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816621 | GGCAATAGGACAGGT[A/G]CAAAGAAATAGGAGG | 405 |
rs587733960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870706 | TACAGATGGGGTTTC[A/G]CCACGTTGCCCAGGC | 405 |
rs587734092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850092 | ATTTTAAAAGCTCCA[A/G]AATATTAACAACTCA | 405 |
rs587734117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822588 | GCTCTGCACTCCTTC[A/C]TCCTTACCTTGCCCT | 405 |
rs587734213 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARNT | GRCh38.p7 | 1:150851053 | CCTCCGCCCGGCAGC[C/T]GCCCCGTCTGAGAAG | 405 |
rs587734261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826825 | AATTTTGTATTTTTT[A/T]AAATAGAGACAGGGT | 405 |
rs587734337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150831243 | AACCCCTACTTTCCA[A/G]TAATACCCAGGCAGC | 405 |
rs587734539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838244 | TTCTAGGTTTTTGCT[C/T]AAGTGCTTCCCAAAA | 405 |
rs587735188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850243 | ATACAAAAATTAGCC[C/G]TCTCCCTCTCCATCT | 405 |
rs587735485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843212 | GATCAAAAGTAACAA[C/T]TCCCTCTCCACTGGA | 405 |
rs587735496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858736 | AAGCAATCCTCCCAC[C/T]TCAGCTTCTGGAATA | 405 |
rs587735850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862882 | ATGGTGAAACTCCGT[C/G]TCTACTAAAAATACA | 405 |
rs587736271 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150871813 | CTCGGGAGGCTGAGG[C/T]GGGAGAATAGCTTGA | 405 |
rs587736430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150847214 | ACACTGGGCGGATCA[C/T]GAAGTCAAGAGATCC | 405 |
rs587736557 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876912 | GCTGTCTCCCTAATC[C/T]CGCCCTCCTTGCGTA | 405 |
rs587736644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150834954 | ATCTGTATACACATA[C/T]AGACATACATACAGA | 405 |
rs587736705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828983 | GAATATGATGATCTC[C/T]TTTTCTTAACTGAGG | 405 |
rs587736738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875847 | GTAGGCCTAACAAGA[G/T]TTAAACCTGGGGCTG | 405 |
rs587736746 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809864 | TCATGGTCAGAGCAT[C/T]CCTGCTGATGTTACT | 405 |
rs587736923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833819 | CTGAGTAAATGGATA[C/T]TGCCTTGTGTTGTAA | 405 |
rs587737083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830268 | AGAGAATCACTTGAA[A/C]CCAGGAGGCGGAGGA | 405 |
rs587737249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836794 | CGCCGGTAATCCCAG[A/C]ACTTTGGGAGGTCAA | 405 |
rs587737407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851585 | GCTCTCTGAAACATG[C/T]GCTGTGTCCACTCAG | 405 |
rs587737663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845571 | CGAGATTACACCACT[A/G]TACTACAGCATGGGT | 405 |
rs587737686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870171 | TTATTCACTCTCTGT[A/G]CCTTAGTTTCCTCAT | 405 |
rs587737893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863383 | AAGAGTGCCAGGTAA[A/T]TTCAGAGAAGATAAT | 405 |
rs587738132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825171 | AGCCAATTTTAGGTT[A/C]TTTTAGATACTAGTC | 405 |
rs587738426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860756 | AGCTACTCGGGAAGC[C/T]GAGGCAGGGAGAATT | 405 |
rs587738431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150817637 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 405 |
rs587738653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867813 | AGAGATCTGGTTGTT[C/T]GAAAGTGTGTAGCAC | 405 |
rs587738726 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150856313 | GGCATCATGGCGGGC[A/G]CCTGTAGTCCCAGCT | 405 |
rs587738877 | snp | A/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810632 | TGGCCAAAGCCAATT[A/T]AAAAAAAAAAAAAAA | 405 |
rs587739029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833746 | ATAAACACTAAACAC[C/G]TACTGAAAGACATAG | 405 |
rs587739202 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150856510 | GCTCATGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 405 |
rs587739375 | snp | A/G | 3.49681e-05 | 0.00418125 | intron-variant | ARNT | GRCh38.p7 | 1:150816759 | ATCCCTCAGGGCCCT[A/G]TAAAGCAGCACATAT | 405 |
rs587739744 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150867545 | AAAAAGAGAGAGATA[C/T]CTTTTAAATAGATAA | 405 |
rs587740179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150876004 | ACGGGGGTTGCGGGT[A/G]GGAGGTAACAGCCTA | 405 |
rs587740227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821487 | AACTGGCAACAATTG[A/G]GCAATAGGTGGCTAC | 405 |
rs587740349 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150838084 | ATCTAATACATTTTT[-/TA]TGTCTCCCCACTGCA | 405 |
rs587740469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819808 | TTAACTGATCTAGAA[C/T]TTCTTTTGGGGGAAT | 405 |
rs587741401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150854782 | GAATTGCCTGAACCC[A/G]GGAGGCAGAGGTTGC | 405 |
rs587741767 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809484 | CATGGTGGCACACAC[A/C]TGTAGTGCCAGCTAC | 405 |
rs587742303 | in-del | -/CTC | 0.00755907 | 0.0610114 | intron-variant | ARNT | GRCh38.p7 | 1:150869541 | GATTTTAGGAAACTA[-/CTC]CTTTTTTTTTTTTTT | 405 |
rs587742698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150813427 | CAACTATAGGTAAGC[C/T]ATTAATTTTACCTAG | 405 |
rs587742727 | snp | A/G | 4.98475e-05 | 0.00499212 | intron-variant | ARNT | GRCh38.p7 | 1:150816938 | TCAAGGGGCTGTAGT[A/G]TATTAGTTCAGCAAG | 405 |
rs587742813 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150813674 | TTTGAGACGGAGTTT[C/T]ACTCTTGTTGCCCAG | 405 |
rs587743207 | snp | C/G | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150871019 | CTAAAATAATAAAAA[C/G]TTTAAAACAAGAAAA | 405 |
rs587743319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863093 | TGGAGGCCAGGCACG[A/G]TGGCTGATGCCTGTA | 405 |
rs587743463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872968 | CCCTCTCCTATGGGG[A/G]AAAAAAATGTGTTCC | 405 |
rs587743559 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876731 | CTTCAGCAGCCCCCA[A/G]CATCCCAGCCCCTGC | 405 |
rs587745058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827774 | CAAAGCTAGTAGCTA[C/T]ACCATTTTACATGTC | 405 |
rs587745150 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150828852 | TGTATTAATATCAAC[A/T]ACAAAAAATAAATAC | 405 |
rs587745154 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809981 | AGACACAATGTGCCT[C/T]ATGTTTGTATGTCTG | 405 |
rs587745209 | snp | A/G | 1.6543e-05 | 0.00287597 | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150852812 | AAAATCCAGCCTGAG[A/G]AAAGCCAACAATAAA | 405 |
rs587745243 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811547 | CACAGGCAGCAAAAA[A/G]AGCCTATGCTCAAAC | 405 |
rs587745582 | snp | A/G | 0.00273547 | 0.0368816 | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861275 | TACTCGGGGTCTGAG[A/G]CAGGAGAATCTTGAG | 405 |
rs587745632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150837877 | AAAAAAAAACCTGCC[A/G]TGCTCTTCCAATATT | 405 |
rs587745673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826424 | CTTAAAAATGCAGAT[C/T]AACTACTAAAGAACA | 405 |
rs587746037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848898 | AACTTAGTTAACAAA[A/C]CAAACAAATAAGAAA | 405 |
rs587746387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849446 | ATTGGTCTTCAGCAA[A/G]AATATCCCCCTTTTC | 405 |
rs587746809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150851693 | TCACCACTCCCTAAT[C/T]TCAAGTACCCAGGGA | 405 |
rs587747202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150855665 | CCAACACTTTAGGAC[A/G]TCGAGATGGGAGGGC | 405 |
rs587747344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150870358 | TTCATATTAACAGTG[A/G]GTTTTACATTCATTT | 405 |
rs587747675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864074 | GCCTATTACTCCCAG[G/T]AACAGCCTATTACTC | 405 |
rs587747996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854006 | CTCCTCTTCCTCCTT[C/T]CTGAATCCCCTAATC | 405 |
rs587748058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150827318 | TGTTCCCTTGTGCCA[C/T]CTGCAGTCAATCTCT | 405 |
rs587748109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826708 | GGAGTACGATGGCGC[A/G]ATCTTGGCTCACTGC | 405 |
rs587748348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815761 | CCCAGCTACTTGGAA[C/G]GCTGAGGCAGGAGAA | 405 |
rs587748492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838305 | ATATCTGCATTTTAC[A/G]GGATTCATTACAGCA | 405 |
rs587748536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821989 | TGAGCCACTGCACCT[C/G]TCCAGCATTTTTACT | 405 |
rs587748544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150817842 | AAAAATTAACCAACC[A/G]AACAAAAAATATATG | 405 |
rs587748718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150873051 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 405 |
rs587748918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150832601 | GTTCCATATGTTCTT[C/T]ATATGCAAACATTCT | 405 |
rs587749050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150845730 | AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 405 |
rs587749410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823675 | CTTGCCTCAGCCTCC[C/T]GAGTGGCTGGGACTA | 405 |
rs587749422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860142 | GTTCATACTGTATAG[C/T]GTACAATATTTTGTG | 405 |
rs587749605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848396 | AGGAGGCGGAGGACG[A/C]AATGAGCAGAGATCG | 405 |
rs587749630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843633 | TTCTTCTAGATAGTT[A/C]CTTAACAAACTACAA | 405 |
rs587749892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862217 | AAATAATGTTTCAAG[C/G]AACATCATTGTGTAT | 405 |
rs587750446 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809230 | GATAATAAATGGGAT[A/C]TGTAATAGACTCAGT | 405 |
rs587750620 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150851184 | GCCAGCCACCCCGTC[C/T]AGGAGAGAGGCGGGG | 405 |
rs587750789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867440 | CCTGTAGTCCAGCTA[C/T]TCAGGTTGCTGAAGT | 405 |
rs587751589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150832882 | TCTTGCTCTTGCCTA[C/T]GTCTTTGCATTAGCC | 405 |
rs587751944 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876839 | GCCAAATCGTCCAAG[A/G]GCAGGGCTACTCACT | 405 |
rs587752019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823463 | TCCTTGAGGCACCAA[C/T]ATTTTTCAATATTAA | 405 |
rs587752386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866140 | GGCACACACCACCAC[A/G]TCCAACTAATCTTTG | 405 |
rs587753023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818611 | ACAAAAATTAGCAGG[C/T]GTGGTGGCGGGCTCC | 405 |
rs587753148 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | ARNT | GRCh38.p7 | 1:150816252 | ACACACAGATGATAA[A/G]TTTTACCTGGGCAGA | 405 |
rs587753479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823810 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 405 |
rs587753990 | snp | C/T | 0.000841301 | 0.0204925 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858399 | TCCTCCACCTTGAAT[C/T]CCAGGTCCAGAGTTT | 405 |
rs587753991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816110 | TGTGATTTTTAATTA[C/G]CTACTCTCAACAAAG | 405 |
rs587754111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150823573 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCCCTCTGT | 405 |
rs587754270 | in-del | -/ATG | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150870076 | ACTTGGAGATTAAGA[-/ATG]ATGACTGTGTAGATG | 405 |
rs587754569 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ARNT | GRCh38.p7 | 1:150847507 | CCCGACTTGGTAAGA[A/T]AAACTACGATAGTCT | 405 |
rs587754653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150817279 | AAATTCATATACAAC[A/G]TATGTACATTCTAAC | 405 |
rs587754797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857894 | CATAACACTAATTAG[C/G]AATTTAATAAATACT | 405 |
rs587754939 | in-del | -/AGA | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150845951 | TATTCCTATTTTTGT[-/AGA]TCCATTTAATAATAA | 405 |
rs587755112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150867936 | CCCCAGCCCTGCCTC[C/T]CATACAGCCTGCGGA | 405 |
rs587755214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872614 | CAAATACCTAATCTC[A/C]TCCCAACTGTTCCCT | 405 |
rs587755312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854329 | TTGGGAGGCCAAGGC[A/G]AGCAGACTACTTGAA | 405 |
rs587755402 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810066 | AAGGAATGATAAAGC[C/T]GCAATCAAGATCACA | 405 |
rs587755583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861953 | CCACACACATTTAAG[C/G]TAGTCTAGGCTAAGA | 405 |
rs587755772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150851088 | GAGCCCCTCCGCCCC[A/G]CAGCCGCCCCGTCCG | 405 |
rs587755990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819918 | GTGAGGTATATGGTA[C/T]GTGAAATATATCTCA | 405 |
rs587756356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861442 | ACATTTGTATACCCA[C/T]GTTCACAGAAGTACT | 405 |
rs587756707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864180 | ACATAGAAAAAGTAA[C/T]GTGTTGTGCTAAGAC | 405 |
rs587756732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825577 | CAGTCTAGGCTGGGC[A/G]CAATGGCTCATGCCT | 405 |
rs587756991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861024 | TCAACATAACCAATC[A/G]CTAGGGAAATGCAAA | 405 |
rs587757583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150826898 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGCGC | 405 |
rs587757738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837010 | AGCAGAGGTTGCAGT[A/G]AGCCGAGATCATACC | 405 |
rs587757973 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150818740 | GGTGACAGAGTGAGA[C/T]ACTGTCTCAATGAAA | 405 |
rs587758125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824083 | CCCGACCTCGGGATC[C/T]GCCTGCCTCGGCCTC | 405 |
rs587758216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150815503 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 405 |
rs587758433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872235 | AGGGATTAGAGGCAC[A/G]AGCCACCACACCTGG | 405 |
rs587759153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150841507 | GAAGCTCGAGTTAAA[C/G]TGGCAGCAAAATGAG | 405 |
rs587759219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856972 | AAACCAAAAAGAAAA[A/T]TTTTAAAGACTTCCT | 405 |
rs587759260 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150851963 | TGAGGCAGGAGAATC[A/G]CTAGAACCCAGGAGG | 405 |
rs587759523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150826124 | TTCACTGTGTTGGCC[A/G]GGCTGGGCTTGAACT | 405 |
rs587759565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863331 | ACTGCACTCCAGCCT[A/G]GGCAACAGAATGAGA | 405 |
rs587759852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865594 | TCCTTCTAACCAAGG[C/G]AACTACCCCTCTCCA | 405 |
rs587759901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869448 | TGCCACTGCACCCCA[C/G]CCTGGGTGACAGAAG | 405 |
rs587759978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823022 | CTCAGGTTCAAGTGA[C/T]TCTCCTGTCTCAGCC | 405 |
rs587760028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868771 | CAGGCGCGGTGGCAC[A/G]TGCCTGTAGTCCCAG | 405 |
rs587760804 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150854260 | TCAACTAAATTTTTT[G/T]ATTTTAAAAAATCTC | 405 |
rs587761349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855249 | AGTACATCCTTTCAC[A/G]CAACCATTAAAAATT | 405 |
rs587761489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861765 | TCATACTATACAAAC[A/C]GTCCTGACTTATAAT | 405 |
rs587761498 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150829436 | TACATTTACACTTTA[-/C]CAAGTTAGTAAAGTA | 405 |
rs587761772 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878253 | ACAACAACGATGAGG[C/T]AGGTTCTACTGCTAT | 405 |
rs587761902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150832105 | CAGTAGGAGGAAAGT[A/G]GGTAAAATAGCATAG | 405 |
rs587762011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150815837 | CCACTGCACTCTAGC[C/T]TGGGCGACAGAGCAA | 405 |
rs587762160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865043 | ATGAAAATATAAATT[A/T]AAATTAATCTGACAG | 405 |
rs587762222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847412 | TTTGTGGCAACAGAG[A/C]GAGACTCCGTCTCAA | 405 |
rs587762560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835196 | AAAAACCAAGTAATT[G/T]TATATGTTATAGAAA | 405 |
rs587762620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819604 | TGAAGTACTGATACA[C/T]GCTACAACATGTATC | 405 |
rs587762788 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150839713 | GGTCATTTGGTAGCA[C/G]GGAGAGTGATATGGA | 405 |
rs587762968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150845317 | CTTAAAATAAAATAA[C/T]AGGCCAGGCACAATG | 405 |
rs587763597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860379 | CACCACCACGCCTGG[C/T]TAATTTTTGTATTTT | 405 |
rs587763840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866562 | AAGGAAATGAGAGAA[A/T]GGGAGCAGAGGACTC | 405 |
rs587763954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873253 | AAGATAGCACCACTG[C/T]ACTCCAGCCTGGGCG | 405 |
rs587764658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150842526 | AAGAAGGAAGGAAGG[A/G]GGGAGGGAGGAAGGG | 405 |
rs587764919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821064 | TTACAATAAAGCTAA[A/G]GAGAAAATGTTATTA | 405 |
rs587764946 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811927 | TGAGGGAAGGGAAGG[A/G]AGAGGAACTTTTATT | 405 |
rs587764992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863235 | GGTGTGGTGGTACAC[A/G]TCTATAATCCCAGCT | 405 |
rs587765313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150876382 | CAAGTCCCCGGGATC[G/T]GGCCCCTCCCCAGGT | 405 |
rs587765518 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150864422 | ATACACCATGGAATA[C/T]TATGCAGCCATAAAA | 405 |
rs587765525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822267 | CTTCAGTGTGATAAG[C/T]GTCTTTTTGTCTGCT | 405 |
rs587765770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847653 | AAAAGACTAGTGGTT[A/G]CCCTCATATCTTTCA | 405 |
rs587765798 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARNT | GRCh38.p7 | 1:150851142 | GGCAGCCGCCCCGTC[C/T]GGGAGGTGGGGGGCA | 405 |
rs587765913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839877 | GAAGATAATGTAATT[C/T]CCTTCCCCCTATTTC | 405 |
rs587766022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150850801 | TGGGAACTGAGGAGC[A/G]CCTCTTCCCGGCCGC | 405 |
rs587766150 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150823904 | CTAGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 405 |
rs587766166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848342 | GCGCCTGTAATCCCA[A/G]CTACTCAGGAGGCTG | 405 |
rs587766595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843333 | AGGCCATTGTGTCAG[A/G]AATGTGTCAATTCCA | 405 |
rs587766779 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150812422 | TCTCTTATCCTATTT[-/G]GTTTTCCACCAAGAC | 405 |
rs587766994 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150817006 | AAACACTGGAAGATT[A/G]CTGACTGGGCAGTGG | 405 |
rs587767073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150830649 | AAAATTTATGCTTTG[C/T]CTAATCTGTAACTTT | 405 |
rs587767114 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878439 | CTTCCATTTTCATGT[A/G]TCGCTCACAAAATGT | 405 |
rs587767154 | snp | C/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150834040 | CCTGGGTTCAAGCAA[C/T]TGTCCTGCCTCAGCC | 405 |
rs587767304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862819 | GCACTTTGAGAGGCC[A/G]AGGCAGGCAGATCAC | 405 |
rs587767314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839183 | CTCTGTGATTCCACT[A/G]TTCTTCTTCCATCCT | 405 |
rs587767492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870485 | CTCTCATGGAACTTA[C/T]ATCCTAAGTATGCTG | 405 |
rs587767939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847559 | ACAAACGAACCTCTC[C/T]TTGGATCTGCATGTA | 405 |
rs587768073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848160 | ACTGGAAACTGTAGT[A/T]GTCTAAAGAGTTTTG | 405 |
rs587768216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150851018 | GCCCGGCAGCCACCC[C/T]GTCTGAGAAGTGAGG | 405 |
rs587768678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867277 | TCATACACCTATAAT[C/G]CCAGCTACTAGGGAG | 405 |
rs587768734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150871627 | CTTAAAAACAGATGG[C/T]GGCGGAGCATGGCGG | 405 |
rs587768944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836160 | ATATTCATTAAAGTA[A/G]AAAATTCTTGAAGCC | 405 |
rs587769407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848313 | GTACAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 405 |
rs587769564 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ARNT | GRCh38.p7 | 1:150850541 | CGCCAGCCTCGGCCT[C/T]CCGAGGTGCCGGGAT | 405 |
rs587770025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874917 | TGAAAATATGGTCAA[C/G]AGGCTGTCATTCTGG | 405 |
rs587770058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828129 | ATCCTTTAAAGAGGG[C/T]AAATTTTAATTACAA | 405 |
rs587770340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150844903 | CAACCTCCACCTCCC[A/G]GGCTCATGCAATTCT | 405 |
rs587770639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150866745 | CCTGAGAAGAGTTAA[C/T]AACCCAGATAAACAC | 405 |
rs587770873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150829423 | AGCTCTGCTCCCATA[C/T]ATTTACACTTTACCA | 405 |
rs587770879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853079 | TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGGCCA | 405 |
rs587771179 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863463 | TATGAAGAGGAAACT[A/C/G]AAGGAAATAAAGAAG | 405 |
rs587771437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864353 | GAAAAAGACCTATTG[G/T]AACCAACCCAAATGT | 405 |
rs587771773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865144 | TGAGGATGGCACAAC[A/G]AAAAGGTAGTTACTT | 405 |
rs587771863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833272 | ACTTTGGGAGGCTGA[C/T]GCAGGCGAATCACTT | 405 |
rs587772067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875207 | GTTTTATTCTATCAC[C/T]CAGCACTTCCTGCAA | 405 |
rs587772643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150860440 | AGGCTGGTCTTTAAC[C/T]CCTGACCTCAAGTGA | 405 |
rs587772871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817698 | CCTGTAATCCCAGCT[A/G]TTTGGGAGGCTGAGG | 405 |
rs587772891 | in-del | -/T | 0.344815 | 0.231323 | intron-variant | ARNT | GRCh38.p7 | 1:150859345 | GTAACAGCTGAGTAC[-/T]TTTTTTTTTTTTTTT | 405 |
rs587772949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150825537 | TTATATAATTCATTA[C/T]GACTCTCACTCATCC | 405 |
rs587772966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860788 | ATTGAACCCAGGAGG[C/T]GGAGACTGCAGTGAA | 405 |
rs587773259 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150871291 | GCATATTAGGCAGTC[C/G]TGGTTTTTTTTTTTT | 405 |
rs587773329 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150847562 | AACGAACCTCTCTTT[-/G]GATCTGCATGTAGTT | 405 |
rs587773547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870697 | ATTTTTTTGTACAGA[C/T]GGGGTTTCACCACGT | 405 |
rs587773649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818476 | AAAATACTGGCCAGG[C/T]ACGGTGGCTTACACC | 405 |
rs587773756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845915 | TCAAAATAAATAAAT[A/T]AATTACAGAACCATT | 405 |
rs587773779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150817733 | TGAATCACTTGAACC[C/T]AGGAGACAGAGGTCA | 405 |
rs587774059 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150813791 | CTGGAATTACAGGCA[G/T]GCGGTACCACACCCG | 405 |
rs587774420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822040 | TGTTGTATGGTAGTA[A/C]ATGATAAAATAGACT | 405 |
rs587774490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842661 | AGGGAAATGGAATTA[C/T]AGGCAGGAACCTTGC | 405 |
rs587774559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867956 | CAGCCTGCGGAACTA[A/T]GAGTCAATTAAACCT | 405 |
rs587774854 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150834111 | TCTAATTTTGTTGTT[G/T]TTTTTTTTTAGTAGA | 405 |
rs587774889 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810211 | AACAAGAAAACAAAA[C/T]AGTCAAAAATAAAAC | 405 |
rs587775086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150814633 | GACCACCTGAGGTGA[A/G]GAGTTCCAGACCAGC | 405 |
rs587775147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857720 | ATGCATATTTCCATA[C/T]ACAGAAAAACATAGT | 405 |
rs587775281 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150849583 | TGAGCACAGGAGTTT[-/A]AAGACCAGCCTGGGC | 405 |
rs587775382 | in-del | -/A | 0.472709 | 0.11358 | intron-variant | ARNT | GRCh38.p7 | 1:150873305 | AACAAACAAACAAAC[-/A]AAAAAAAAAACAAAA | 405 |
rs587775602 | in-del | -/T | 0.00716694 | 0.0594315 | intron-variant | ARNT | GRCh38.p7 | 1:150860433 | TTGGCCAGGCTGGTC[-/T]TTTAACTCCTGACCT | 405 |
rs587775627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150856762 | GCAAGACTCTGCCTC[A/G]AAAATAAATAAGTAA | 405 |
rs745370230 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858765 | TAGCTAGGACTATAG[A/G]CCCGCACTACCACAC | 405 |
rs745371289 | snp | G/T | 3.31345e-05 | 0.00407016 | intron-variant | ARNT | GRCh38.p7 | 1:150823357 | CTACCTGAAAAAGTT[G/T]TCATGCCATCAGTGG | 405 |
rs745385044 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835054 | GACTGCTTGAGGGCA[A/G]GAGTTTGAGGCTGTA | 405 |
rs745385830 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816931 | GGGCCAGTCAAGGGG[C/T]TGTAGTATATTAGTT | 405 |
rs745426616 | snp | A/C | 1.65946e-05 | 0.00288046 | missense | ARNT | GRCh38.p7 | 1:150826603 | GAATTCTACAATATT[A/C]TTTCCTAAGAGTTCC | 405 |
rs745432347 | snp | C/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877489 | GCCTGCTATGGAACC[C/G]GTAGTCTAAAAGGAT | 405 |
rs745478924 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150833590 | ATCCTACCCATAATT[G/T]CTAGCAACTATCCTC | 405 |
rs745497037 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150827316 | GATGTTCCCTTGTGC[A/C]ATCTGCAGTCAATCT | 405 |
rs745521026 | in-del | -/G | 1.70388e-05 | 0.00291875 | frameshift-variant | ARNT | GRCh38.p7 | 1:150812032 | GTTCTATTCTGAAAA[-/G]GGGGGGAAACATAGT | 405 |
rs745545111 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861174 | GGAAATGTAAAATGG[C/T]GTAACAGCAATAGAA | 405 |
rs745572757 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849625 | AAAATTAGCCAGGTA[G/T]TATGGCTCACACCTG | 405 |
rs745601404 | snp | A/G | 1.68247e-05 | 0.00290035 | missense | ARNT | GRCh38.p7 | 1:150812049 | GGGGGAAACATAGTT[A/G]GATCAGGGAATTCTT | 405 |
rs745603389 | snp | A/G | 1.65037e-05 | 0.00287256 | intron-variant | ARNT | GRCh38.p7 | 1:150817209 | CTGAACCACCTGTGG[A/G]ATACAATGATAAAAA | 405 |
rs745620916 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828024 | CTTAATGAGTTGTTT[A/T]TATATTCCTGGTACA | 405 |
rs745628683 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844546 | CAGGAGCATCAGCAA[C/T]GAACAAATACTAAGT | 405 |
rs745643618 | snp | G/T | 0.000129241 | 0.00803764 | intron-variant | ARNT | GRCh38.p7 | 1:150861201 | AGAAAACAGTATGGA[G/T]ATGCCTCCAAAAATT | 405 |
rs745691074 | snp | C/G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825759 | GGGGCTGAAACAGGA[C/G/T]AATCGCTTGAACCTA | 405 |
rs745712465 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816538 | AAATTTGATAACAAT[C/T]TGGAAAAGACAAGAA | 405 |
rs745736005 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870201 | TCTGTAAAACAAGAA[C/T]AATAATACTTACCTA | 405 |
rs745740973 | snp | C/T | 1.9017e-05 | 0.00308353 | intron-variant | ARNT | GRCh38.p7 | 1:150876511 | CTTCGGCCCCTCCCC[C/T]TTAGAGGCGCCCCAG | 405 |
rs745777019 | snp | C/G | 0.000131907 | 0.00812009 | missense | ARNT | GRCh38.p7 | 1:150813249 | AACTTGAACGATGAT[C/G]AGGCTGCTGGCCCTG | 405 |
rs745778724 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150842237 | AGCAAAGTTCCCTCA[A/G]CTCACCCACTTTCTG | 405 |
rs745792977 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150852630 | AAATTTTCTGAGATA[C/T]ATGAATATTTATAGT | 405 |
rs745800607 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854992 | AAGAAAAAAAAGTCT[C/T]GCCATTTTCCCCAGG | 405 |
rs745806292 | snp | C/T | 2.18955e-05 | 0.00330867 | intron-variant | ARNT | GRCh38.p7 | 1:150836512 | CGCAAGAAAAAGAAA[C/T]AGAAGTTAATATTTT | 405 |
rs745825601 | in-del | -/CTC | | | intron-variant | ARNT | GRCh38.p7 | 1:150813515 | AAATTAATTCTTCTT[-/CTC]CTCCAGGCAGCCTTT | 405 |
rs745886785 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150817907 | AACAGATGATTATTT[C/T]ACCCTTTTTTACCTG | 405 |
rs745889786 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849079 | ATGGTAGTGCATGCC[G/T]GTAATCCCAGCTACT | 405 |
rs745927218 | snp | A/G | 3.33261e-05 | 0.0040819 | intron-variant | ARNT | GRCh38.p7 | 1:150842475 | TCATCCGACCTAAAA[A/G]TAGAATTAATGAACT | 405 |
rs745948238 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838630 | TAAATTGGTGGCATT[A/G]AGGGAATACTTGATT | 405 |
rs745954301 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854993 | AGAAAAAAAAGTCTC[A/G]CCATTTTCCCCAGGC | 405 |
rs745988037 | snp | C/T | 1.65559e-05 | 0.00287709 | intron-variant | ARNT | GRCh38.p7 | 1:150829872 | TCTGCTCTAATTGAA[C/T]GGGAATATAGATGTG | 405 |
rs746040398 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876909 | CCAGCTGTCTCCCTA[A/G]TCTCGCCCTCCTTGC | 405 |
rs746068568 | in-del | -/ATC | 0.000350301 | 0.0132298 | cds-indel | ARNT | GRCh38.p7 | 1:150846295 | ATCGTTAGACATCTG[-/ATC]ATCATCACACCTGAA | 405 |
rs746084622 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813733 | CACCGCAACCTCTGC[C/T]TCCTGGGTTCAAGCG | 405 |
rs746099908 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150874783 | ATCTAAAAATTGCAG[A/T]AGCAAGCAGCCAAAG | 405 |
rs746132426 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150862437 | GGTCATTTTCTTGGT[-/A]AAAAAACAATTACCA | 405 |
rs746138053 | snp | C/T | 1.75496e-05 | 0.00296217 | intron-variant | ARNT | GRCh38.p7 | 1:150831775 | GGACTCTGTGAGGAA[C/T]CAACTGTACCAAGGG | 405 |
rs746147835 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150812546 | GTGTAAATAGACCAT[G/T]ATGGCTATAATCATT | 405 |
rs746205086 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150848770 | TTCCAGAGCTTAAGC[A/G]ATCCACCCACCTCAG | 405 |
rs746208662 | snp | A/G | 4.30506e-05 | 0.00463933 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817924 | CCCTTTTTTACCTGG[A/G]TGCCAGCTGTCCTGA | 405 |
rs746281087 | snp | A/G | 1.93205e-05 | 0.00310803 | synonymous-codon, intron-variant | ARNT | GRCh38.p7 | 1:150818027 | TGGTTCTTGGCTAGA[A/G]TTCCTAGGAAACCAG | 405 |
rs746311845 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865086 | AAGTAATAGAAGTAG[A/G]AAGACAAGATTAATA | 405 |
rs746326566 | snp | A/G | | | synonymous-codon | ARNT | GRCh38.p7 | 1:150823321 | GGAACATGACAGACA[A/G]CACTTGGCCTTTTAA | 405 |
rs746331526 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809796 | GTTTTCAAGTCCCGA[C/T]TCTTCCCCTCTCTCC | 405 |
rs746393087 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861866 | TCTGTAAATTACATA[A/G]TATCCAGTACTTTAT | 405 |
rs746397576 | snp | A/C | 1.66167e-05 | 0.00288237 | intron-variant | ARNT | GRCh38.p7 | 1:150842380 | AAAGGATAGAAAAAG[A/C]AGCATCATCTGCTTC | 405 |
rs746406064 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | ARNT | GRCh38.p7 | 1:150814140 | GCGATGCAGTTGGGG[C/T]ACCAGGGAGGGACAT | 405 |
rs746416559 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821511 | TGGCTACCAAATTAT[C/T]ACAACAGTACAGTAT | 405 |
rs746446716 | snp | A/C | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810701 | GGGTGAGGGTAGTAA[A/C]CTGTATCCGCATTTA | 405 |
rs746455356 | snp | C/T | 0.000605961 | 0.0173958 | intron-variant | ARNT | GRCh38.p7 | 1:150816772 | CTGTAAAGCAGCACA[C/T]ATATACGGGGCTCAC | 405 |
rs746464139 | in-del | -/T | 3.42073e-05 | 0.00413552 | intron-variant | ARNT | GRCh38.p7 | 1:150813361 | TACAGCAAGGAAGAA[-/T]AAACAACTCCAATCT | 405 |
rs746581148 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816187 | AATAGAAAACACTGA[-/T]TTTTACATACGGAAA | 405 |
rs746608018 | snp | C/T | 0.000266064 | 0.0115309 | intron-variant | ARNT | GRCh38.p7 | 1:150853205 | AGAATTGCTGGAACC[C/T]GGGAGGTGGAGGTTT | 405 |
rs746627628 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150814598 | TATAATCCCAGCACT[C/T]TGGGAGGCCAAGGCA | 405 |
rs746636601 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861709 | GGCATGAGTCACCAC[A/G]CCCAGCCAGGGTTTC | 405 |
rs746647320 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821105 | AAGGAAGAGAAAATG[C/T]ATTTACAGCACTGTA | 405 |
rs746655511 | in-del | -/CT | | | intron-variant | ARNT | GRCh38.p7 | 1:150845893 | GGCAACAGAGCAAGA[-/CT]CTGTCTCAAAATAAA | 405 |
rs746660811 | snp | C/G | 0.000115334 | 0.00759299 | synonymous-codon | ARNT | GRCh38.p7 | 1:150834555 | CATTCGGCAAATAAA[C/G]GATCTCCTTGAGCCC | 405 |
rs746667101 | snp | A/G | 2.45637e-05 | 0.00350446 | stop-gained, synonymous-codon, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858374 | GCTTAATAGCCCTCT[A/G]GACAATGGCTCCTCC | 405 |
rs746677007 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150842676 | TAGGCAGGAACCTTG[-/C]CTGTAACTCTACAAA | 405 |
rs746690327 | in-del | -/A | 7.32131e-05 | 0.00604989 | intron-variant | ARNT | GRCh38.p7 | 1:150817485 | AAAAAAATTTTTTTT[-/A]AAAAAGAATCTGGAG | 405 |
rs746701385 | in-del | -/TTGTC | | | intron-variant | ARNT | GRCh38.p7 | 1:150828421 | ATTTTATCCATTGAA[-/TTGTC]TTGTCACCTTTGCTG | 405 |
rs746754370 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861878 | ATAATATCCAGTACT[G/T]TATTATAAAGTAGAA | 405 |
rs746810391 | in-del | -/TTATT | | | intron-variant | ARNT | GRCh38.p7 | 1:150859145 | ACAAATATTTATAAC[-/TTATT]TTATTTATTGTGATT | 405 |
rs746820684 | snp | A/T | 1.65291e-05 | 0.00287476 | intron-variant | ARNT | GRCh38.p7 | 1:150839395 | GAAAACTTTCAAGAG[A/T]TTCACCCAGATTCCA | 405 |
rs746852019 | snp | A/G | 1.67643e-05 | 0.00289515 | intron-variant | ARNT | GRCh38.p7 | 1:150823382 | CAGTGGAACTCATAG[A/G]AAATTTTCATTACAA | 405 |
rs746899081 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816611 | CCTAGAACATGGCAA[C/T]AGGACAGGTGCAAAG | 405 |
rs746919007 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860745 | CCTGTAATCCCAGCT[A/T]CTCGGGAAGCTGAGG | 405 |
rs746984591 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150814587 | TGGCTCATGCCTATA[A/G]TCCCAGCACTTTGGG | 405 |
rs747007166 | in-del | -/AC | | | intron-variant | ARNT | GRCh38.p7 | 1:150875503 | TCCGCCCCACGCAAC[-/AC]ACACACACATATCTC | 405 |
rs747035639 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150818479 | ATACTGGCCAGGCAC[A/G]GTGGCTTACACCTGT | 405 |
rs747042920 | snp | A/G | 5.17478e-05 | 0.00508638 | intron-variant | ARNT | GRCh38.p7 | 1:150831791 | CAACTGTACCAAGGG[A/G]AAATATTTACTATTT | 405 |
rs747081194 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854760 | TACTCGGGAGGCTGA[C/G]GCATGAGAATTGCCT | 405 |
rs747085261 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865814 | CTTTCTTGGTTTACT[A/G]TCTCCTACTGGTAGA | 405 |
rs747092222 | snp | C/T | | | missense | ARNT | GRCh38.p7 | 1:150812067 | TCAGGGAATTCTTCA[C/T]TGTTGTAGCTGTTGC | 405 |
rs747095702 | snp | A/G | 1.65359e-05 | 0.00287536 | intron-variant | ARNT | GRCh38.p7 | 1:150817246 | TTAAAGATTTAACAT[A/G]ACAATTCAATAACCC | 405 |
rs747150620 | snp | A/C | 1.87704e-05 | 0.00306347 | intron-variant | ARNT | GRCh38.p7 | 1:150831946 | AAAAAAAAAAATCTA[A/C]CCGTAAAACTCAAAG | 405 |
rs747257592 | snp | C/G | 5.19332e-05 | 0.00509548 | intron-variant | ARNT | GRCh38.p7 | 1:150813129 | CCTCCTGGACCCTTT[C/G]TCTCCCAGCTTCTAA | 405 |
rs747258767 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871413 | TCAAGCGATTCTCCC[G/T]CCTCAGCCTCCCGAG | 405 |
rs747271228 | snp | C/G | 7.85639e-05 | 0.00626704 | missense, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150876547 | CGTCTCCTCACCGGG[C/G]TTGGCAGTAGTCGCC | 405 |
rs747277179 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817421 | GTCCAATTCTGTTTG[C/T]TGTTGCTGCTGCCTA | 405 |
rs747317209 | snp | C/T | 1.67321e-05 | 0.00289236 | intron-variant | ARNT | GRCh38.p7 | 1:150823170 | AGGAAAAACAGTTTT[C/T]TCACACTCCTGTATA | 405 |
rs747385144 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150821146 | CGTTATCATAAGCTT[A/G]TATCATCTTACAAGA | 405 |
rs747433085 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819833 | GGGAATGAAAATATT[C/T]TGAAATTAGACTGCA | 405 |
rs747444055 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150859970 | CGTGATTGCACCACT[A/G]CACTCCACCCTGGGC | 405 |
rs747473531 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838516 | CTATTTCAATGTATA[C/T]AGCTACAAAGTATGT | 405 |
rs747494138 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840526 | CAGAATTTGAAGATT[C/T]TGAAGTTTTATTTGG | 405 |
rs747529346 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856443 | AGACTCCATCTCAAA[A/G]AAATAAAAAATAAAA | 405 |
rs747561564 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150837265 | TTTTTCAGCAGCAAG[A/C]TTATACTAAGAATAA | 405 |
rs747580559 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840691 | GAGTGGAATGGAGAG[A/G]AGGATGATTAAAGGT | 405 |
rs747586181 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846352 | GCATTACACTTGTTA[C/T]ATCTATTTCACTCTG | 405 |
rs747587987 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150833111 | AGCACAATGTAGTCA[C/T]GTAATCATCCAAGGT | 405 |
rs747636674 | snp | A/C/T | 3.29828e-05 | 0.00406085 | missense | ARNT | GRCh38.p7 | 1:150817082 | GAGAAAGAAACATAC[A/C/T]CGCATTGATGTTGTG | 405 |
rs747677643 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828640 | AGCCAGAAGTCCTTC[C/T]GACCCACAACAGTTT | 405 |
rs747711331 | snp | C/T | 1.69479e-05 | 0.00291095 | intron-variant | ARNT | GRCh38.p7 | 1:150836236 | GTCTCAGGAAAAAAA[C/T]AAGAAAGGACTTCTC | 405 |
rs747712283 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820944 | TGTAAACTTCTGACT[C/T]TCCCAAAACGTTACT | 405 |
rs747788454 | snp | C/T | 1.6519e-05 | 0.00287388 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836371 | TGTGCTGCCAAACCA[C/T]TCAGACTGTGGCTGG | 405 |
rs747833504 | snp | A/C | 2.05434e-05 | 0.00320488 | intron-variant | ARNT | GRCh38.p7 | 1:150818040 | GAGTTCCTAGGAAAC[A/C]AGAGTAGACAGTAAA | 405 |
rs747846383 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865325 | AGAATAAGAGAAGAA[A/G]AGCAATAATTTTTTT | 405 |
rs747864356 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877191 | CGCTTGAACCTGGGA[A/G]GCAGAGGTTGCAGTG | 405 |
rs747917577 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857038 | CATTTCAAAAATCTG[A/G]AAAATCAAAAACAAA | 405 |
rs747942817 | snp | G/T | 2.30593e-05 | 0.00339545 | intron-variant | ARNT | GRCh38.p7 | 1:150839670 | CTGCATGGAAAGAAA[G/T]AGAAGCCCCATCCAG | 405 |
rs747959547 | snp | A/T | 1.6782e-05 | 0.00289668 | intron-variant | ARNT | GRCh38.p7 | 1:150826638 | ATACAGAAAGAAGAG[A/T]AAGATATATACTTTT | 405 |
rs747965710 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150851949 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATCGC | 405 |
rs748012368 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852414 | GTCCAGTTCTCAGCT[A/G]ACCAGCTGAGAATGC | 405 |
rs748021888 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859495 | GGGACTACAGATGGG[C/T]ACCACCACACCTCGG | 405 |
rs748024329 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150841996 | AGGAAAATAGGTGTG[A/C]GTTTCCTAGAGGTGT | 405 |
rs748035355 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150830509 | ATATATTAATTCCTA[C/T]ATTTTACCCATGTTA | 405 |
rs748056442 | snp | C/G | 4.94507e-05 | 0.00497221 | missense | ARNT | GRCh38.p7 | 1:150816851 | GAGAATAGCTGTTGG[C/G]TGGCAGGGACAGTGC | 405 |
rs748069778 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875233 | TGCAATGTAATTTTT[G/T]CGATTAATTTTACCT | 405 |
rs748081405 | in-del | -/TGAAATAATCATCT | 2.26091e-05 | 0.00336215 | intron-variant | ARNT | GRCh38.p7 | 1:150818061 | GACAGTAAAGAGGGG[-/TGAAATAATCATCT]GTGGAGAGGGAGGAA | 405 |
rs748087978 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150824159 | GACTCAAGCTTTCTT[A/G]TTAGGTTGGTGCAAA | 405 |
rs748127684 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150828674 | AAGTTTATATGATGC[A/G]TCAATTCAGAGATGG | 405 |
rs748177172 | in-del | -/ATTTTT | | | intron-variant | ARNT | GRCh38.p7 | 1:150821646 | TATACGTTGTGATAC[-/ATTTTT]ATTTTTATTTTTTTT | 405 |
rs748178328 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150848312 | AGTACAAAAATTAGC[C/T]GGGCATGGTGGCAGG | 405 |
rs748192872 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870424 | ATACTAGGCACCCAC[C/T]GTAAGCACTGCAATG | 405 |
rs748206590 | in-del | -/CTG | | | intron-variant | ARNT | GRCh38.p7 | 1:150825000 | CAAGTAGCTGGGACT[-/CTG]ACAGGCATGAGCCAC | 405 |
rs748207091 | snp | C/T | | | missense | ARNT | GRCh38.p7 | 1:150813242 | TCACTAGAACTTGAA[C/T]GATGATGAGGCTGCT | 405 |
rs748240537 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | ARNT | GRCh38.p7 | 1:150813263 | TGAGGCTGCTGGCCC[C/T]GCCACTGTGGCCAGA | 405 |
rs748251027 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150826837 | TTTTAAATAGAGACA[A/G]GGTTTCACCATGTTG | 405 |
rs748268727 | snp | C/T | 3.26036e-05 | 0.00403741 | intron-variant | ARNT | GRCh38.p7 | 1:150817876 | TTGCAAATGACCACC[C/T]CCTGGGTGACTGCTC | 405 |
rs748269933 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809962 | TTCTGATTCCTGAAA[C/T]TAAAGACACAATGTG | 405 |
rs748301139 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150843659 | TACAAACTTCTTTTT[C/T]TTCAAAAAGTTGAGC | 405 |
rs748338917 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150825490 | AGATATTTTCAGGAG[A/C]TGGAGCCTGAGAATG | 405 |
rs748347258 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150812631 | TGTGTGTCATCCTTA[C/T]GCAGGGGCCATGCTA | 405 |
rs748380917 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150866052 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 405 |
rs748388183 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839486 | GCCATCAGTGGATGT[A/G]TTGCCAGTTCCCCGC | 405 |
rs748439574 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150874727 | GAGGGGACAGGAGAG[A/C]GGGGAGAGGAGAAAG | 405 |
rs748469847 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844156 | GATTAACTTCTCATT[G/T]TAGAGATGGTTCACA | 405 |
rs748553730 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859960 | TGCAGTGAGTCGTGA[C/T]TGCACCACTGCACTC | 405 |
rs748595298 | snp | A/C | 1.65244e-05 | 0.00287436 | missense | ARNT | GRCh38.p7 | 1:150852766 | CAGTCTCTTACCTCA[A/C]AAATTTACTGTTCCC | 405 |
rs748632201 | in-del | -/TTG | | | intron-variant | ARNT | GRCh38.p7 | 1:150834103 | CACGCCCGTCTAATT[-/TTG]TTGTTGTTTTTTTTT | 405 |
rs748669896 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810826 | ACCCAATCTCAAGAT[C/T]GGAGGGAGCAAAGAG | 405 |
rs748763301 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150864157 | GTGGTAACTATTTAT[A/G]TATCTAAACATAGAA | 405 |
rs748766735 | snp | A/C | 1.74163e-05 | 0.00295091 | intron-variant | ARNT | GRCh38.p7 | 1:150812130 | TAAAAGAAAAAGATT[A/C]AGTTTGGGTCACACA | 405 |
rs748796542 | snp | A/G | 3.97915e-05 | 0.00446029 | intron-variant | ARNT | GRCh38.p7 | 1:150836503 | CAGTTCCTGCGCAAG[A/G]AAAAGAAATAGAAGT | 405 |
rs748813479 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819526 | CCAAATGTCCATTAA[C/T]GAACATACAGACAGT | 405 |
rs748863620 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150855571 | CGTCTCAAAAAAAAA[-/T]AAATAAAAATTATGT | 405 |
rs748879208 | snp | A/G | 4.95103e-05 | 0.00497521 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823199 | TAATACATACTTCAC[A/G]TTGGTGTTGGTACAG | 405 |
rs748905194 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150818149 | CATCTGTAGGTGGAA[A/C]AATCAATAAATCCTT | 405 |
rs748927045 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | ARNT | GRCh38.p7 | 1:150823324 | ACATGACAGACAGCA[C/T]TTGGCCTTTTAATTT | 405 |
rs748991146 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150835248 | TTTATTATACAGAAA[C/T]GAAGAACAACTTTTG | 405 |
rs749033952 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860789 | TTGAACCCAGGAGGC[G/T]GAGACTGCAGTGAAC | 405 |
rs749051952 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828601 | TCAAGACCTCTTTTT[C/T]ACCAACCTCTTTCAC | 405 |
rs749084006 | snp | A/C | 1.65597e-05 | 0.00287743 | intron-variant | ARNT | GRCh38.p7 | 1:150829858 | ATGAGTCCTGAAGAT[A/C]TGCTCTAATTGAACG | 405 |
rs749092402 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873382 | GACCACCTACCCACC[A/G]AGTTCTACTTGCCAG | 405 |
rs749097163 | snp | A/G | 3.29761e-05 | 0.00406041 | intron-variant | ARNT | GRCh38.p7 | 1:150816896 | TTACTCTGATCTGTG[A/G]ACCAAAAGGAGTTGG | 405 |
rs749127284 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150856691 | TCCCTTGAACCAGAG[A/T]GGTGGAGATTGCAGT | 405 |
rs749130969 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872394 | AGGTGAAAATTAGCT[A/T]AAAAAAATTTTCTTC | 405 |
rs749154828 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846074 | AAATATACCGCCAGT[C/T]TGAAGCCATGTCACC | 405 |
rs749178667 | in-del | -/CCC | 0.0841029 | 0.187024 | utr-variant-5-prime, cds-indel, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876596 | ACCGCCGCCGCGCCA[-/CCC]CCCCCCCCAGTGGGA | 405 |
rs749188658 | snp | C/T | 3.32336e-05 | 0.00407624 | intron-variant | ARNT | GRCh38.p7 | 1:150836262 | TTCTCATTCATTTCC[C/T]ATACACATAACTCTC | 405 |
rs749236310 | snp | C/T | 0.000167666 | 0.00915449 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858481 | AGGAAAATAATGAAG[C/T]AAACATTTTTAAAAA | 405 |
rs749270912 | snp | A/G | 1.82563e-05 | 0.00302123 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150818013 | GAGAGTGTAGGCCGT[A/G]GTTCTTGGCTAGAGT | 405 |
rs749279539 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844670 | TATTGCCTAATATTT[A/T]ATAAAAACTTTCTAA | 405 |
rs749281228 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865944 | AATTCTAAATTAGAA[C/T]TTATTTTCCCTCAGA | 405 |
rs749294419 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150824612 | GGCGTGCACCATCAC[A/G]CCCAGCTAATTTTTG | 405 |
rs749358327 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878540 | GTTGTATATGTACTG[C/T]GCAGATTACATTGAT | 405 |
rs749397031 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150841621 | TAAGTCACCCCCAAA[C/T]CACAGATACTAGAAA | 405 |
rs749440287 | snp | A/G | 9.88468e-05 | 0.00702948 | missense | ARNT | GRCh38.p7 | 1:150814127 | GCAGCAGCACCAGGC[A/G]ATGCAGTTGGGGCAC | 405 |
rs749523683 | snp | A/G | 4.99081e-05 | 0.00499515 | intron-variant, missense | ARNT | GRCh38.p7 | 1:150842448 | CTCTCTTTATCCGCA[A/G]AGCTCTGCTCATCAT | 405 |
rs749525889 | snp | C/T | 6.60262e-05 | 0.00574532 | missense | ARNT | GRCh38.p7 | 1:150829211 | CTCATGTCTGTACAG[C/T]TGGGAGAACTAGTTA | 405 |
rs749638068 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150848823 | AGGTGTAAGCCACCA[A/G]GCCCAGCCTGAAATT | 405 |
rs749658569 | snp | C/T | 1.87362e-05 | 0.00306068 | intron-variant | ARNT | GRCh38.p7 | 1:150852885 | ATTTCTCAACACAAG[C/T]TACCGGAACACCCAC | 405 |
rs749659456 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150833711 | TTCTACAGAATCCTA[A/G]AACGTACAGTATATA | 405 |
rs749693130 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809809 | GACTCTTCCCCTCTC[C/T]CCCAAGAACCCAGGC | 405 |
rs749702096 | snp | A/G | 3.29614e-05 | 0.00405951 | intron-variant | ARNT | GRCh38.p7 | 1:150817445 | CTGCCTATATGTCAA[A/G]GGCCAGTTGACAAGA | 405 |
rs749713247 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150865728 | AGGAAAACTAACACC[A/C]ATGTATGCATACTAC | 405 |
rs749713602 | snp | A/C | 3.29734e-05 | 0.00406025 | intron-variant | ARNT | GRCh38.p7 | 1:150832446 | TCAGACTGCCCTATC[A/C]AAGAACTTTCCACAG | 405 |
rs749717280 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150849924 | ACAAAAATTAGCCAG[C/G]TGTGGTAGTCCCAGC | 405 |
rs749721628 | in-del | -/AA | | | intron-variant | ARNT | GRCh38.p7 | 1:150833051 | TCATAACAACTTTAT[-/AA]AGTCAGTATTAACAT | 405 |
rs749739532 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809921 | AGTGAGGGGGGAGGC[A/G]TGCAATGTGATCAGA | 405 |
rs749829643 | snp | A/C | 1.64792e-05 | 0.00287042 | intron-variant | ARNT | GRCh38.p7 | 1:150817895 | GGGTGACTGCTCAAC[A/C]GATGATTATTTCACC | 405 |
rs749853270 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838612 | TCTTTCTAATCATTT[-/G]ATTAAATTGGTGGCA | 405 |
rs749894813 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150835579 | GTACTCCAGCCTAGG[C/T]AAGAGAGAGACCCTG | 405 |
rs749906325 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853359 | TCCTAGAGTAGCAGT[C/T]AATCTTTGCCAGAGT | 405 |
rs749918104 | snp | G/T | 1.64746e-05 | 0.00287002 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839468 | GAAAGACGGCTTATA[G/T]GAGCCATCAGTGGAT | 405 |
rs749966267 | snp | G/T | 1.64939e-05 | 0.0028717 | missense | ARNT | GRCh38.p7 | 1:150814085 | GACTCACCAAAGTTA[G/T]ATCCACGATTGGTGA | 405 |
rs749974274 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854112 | TTTTTAAGAGACAAG[C/G]TCTCACTCTGTTACT | 405 |
rs749979422 | snp | C/T | 1.64874e-05 | 0.00287113 | missense | ARNT | GRCh38.p7 | 1:150839584 | TACAGGTGGGTACCA[C/T]ATCTGACAGTTCTGT | 405 |
rs750029409 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150852603 | CTCTAGAGATATTAA[C/T]GGAATGCTTAAAAAT | 405 |
rs750049131 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810378 | CATTGGAAACTCAAC[G/T]TTTTGGTTTCGTAAA | 405 |
rs750094376 | snp | G/T | 1.65124e-05 | 0.00287331 | missense | ARNT | GRCh38.p7 | 1:150829113 | GCTGGTAGCCAACAG[G/T]AGCCACACAGCGGTG | 405 |
rs750125882 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150869379 | CTACTCGCGAGGATG[A/T]GGCAGGAGAATGGCG | 405 |
rs750137064 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150826390 | TCCATAATTTCAAAG[C/T]ATTAGTCCTTTTCTA | 405 |
rs750150223 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150823578 | TTTTTTGAGACGGAG[G/T]CTCCCTCTGTCGCCC | 405 |
rs750177207 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852850 | AGCCTGCTGATAATA[C/G]AAAACATTAAGAAGT | 405 |
rs750267263 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820561 | ACTCAGGGGACTGAG[A/G]TGGGAGGATCACTTG | 405 |
rs750295915 | snp | C/G | 3.29451e-05 | 0.00405851 | missense | ARNT | GRCh38.p7 | 1:150832355 | CTGTTCCTCACAAAG[C/G]TCAGCCTATTCACAG | 405 |
rs750307666 | snp | C/T | 1.64743e-05 | 0.00287 | missense | ARNT | GRCh38.p7 | 1:150817403 | ATCTCTTCCTGGTAC[C/T]ATGTCCAATTCTGTT | 405 |
rs750399064 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150841924 | CGCAAGAAAGGATTC[C/G]GTCACCAAAGCAACA | 405 |
rs750449068 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | ARNT | GRCh38.p7 | 1:150823305 | TTCTTAGACCGGAAC[C/T]GGAACATGACAGACA | 405 |
rs750526813 | in-del | -/CTGT | | | intron-variant | ARNT | GRCh38.p7 | 1:150844809 | AAAACTGTTTCCTTA[-/CTGT]CTTTTTTTTTTTTTT | 405 |
rs750562341 | snp | A/G | 1.75919e-05 | 0.00296574 | intron-variant | ARNT | GRCh38.p7 | 1:150846241 | ATTATATATTACAAT[A/G]TATTACCTACTACAA | 405 |
rs750574542 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | ARNT | GRCh38.p7 | 1:150816285 | AGCCTGAGCGGGTAG[C/T]AGGGGTCCAAGTTGG | 405 |
rs750632567 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876949 | CAATGACCGAGTAAC[A/G]TCATTGAAATGCAAT | 405 |
rs750633471 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865665 | AAAGGTCTTACAGTC[-/T]TAGTGAACACGACGT | 405 |
rs750685316 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150815213 | AATCTTTCTTTAGAC[A/G]GTGTATTTATTGTGC | 405 |
rs750727366 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150830300 | GCAGTGAGCCGAGAT[C/T]GCACTACTGCACTCC | 405 |
rs750743583 | snp | C/G | 1.6483e-05 | 0.00287076 | missense | ARNT | GRCh38.p7 | 1:150817160 | CTGACTTCTCAAGGG[C/G]CTTGCTGTGTTCTGG | 405 |
rs750754277 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150822604 | TCCTTACCTTGCCCT[A/G]TCTATCTCTTCATCT | 405 |
rs750762964 | snp | G/T | 1.67646e-05 | 0.00289517 | missense | ARNT | GRCh38.p7 | 1:150812081 | ATTGTTGTAGCTGTT[G/T]CTCTGATCTCCCAGC | 405 |
rs750794396 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824927 | AGTGCAGTGGGGCAA[C/T]CTTGGGTCACTGCAA | 405 |
rs750861496 | snp | C/G | 0.000190132 | 0.00974833 | intron-variant | ARNT | GRCh38.p7 | 1:150861319 | TGGGAAACACAGCAA[C/G]ACAACATCGCAAAAA | 405 |
rs750871502 | in-del | -/A | 0.0338756 | 0.125659 | intron-variant | ARNT | GRCh38.p7 | 1:150861330 | GCAAGACAACATCGC[-/A]AAAAAAAAATTAAAT | 405 |
rs750962650 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811741 | CAAATCAACACTATA[C/T]AATTTCAGGTCAGGA | 405 |
rs751002810 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150861422 | GAAAGCAGGGTCTCA[A/C]AGAAACATTTGTATA | 405 |
rs751010612 | snp | A/C | 1.64874e-05 | 0.00287113 | missense | ARNT | GRCh38.p7 | 1:150829148 | ACAAAAGTGAAGATA[A/C]CCTCAATGTTGTGTC | 405 |
rs751055466 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150823928 | GCTCACTACAACCTC[C/T]GACTCCCTGGTTCAA | 405 |
rs751059210 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150849534 | CTCATGCCTGTAATC[A/C]CAACACTTTGGAAGG | 405 |
rs751191329 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | ARNT | GRCh38.p7 | 1:150817065 | GAATTTAAAAGGATA[A/G]TGAGAAAGAAACATA | 405 |
rs751191450 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824825 | GCTTTAGTCTTGTTT[A/T]GCTTTTATTTTTTAA | 405 |
rs751200394 | snp | A/G | 1.65715e-05 | 0.00287845 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150829972 | GGTCATCATCTGGGA[A/G]GGAAACACCTTCAGA | 405 |
rs751217442 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868467 | ACCAAGTTTCTAGGA[A/G]AGGCTCAATTATGGA | 405 |
rs751252734 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840845 | TTTTTAAAAGCCCAT[G/T]AAGTTTCTCAGTGTC | 405 |
rs751286930 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150864874 | AAAACAAAATGGTTT[C/T]CTTTAAATCAAAAAA | 405 |
rs751289486 | snp | A/G | 1.64844e-05 | 0.00287087 | intron-variant | ARNT | GRCh38.p7 | 1:150834651 | ACGCCCTGAAGGAAG[A/G]TGTGAAGAGCAGTCT | 405 |
rs751366135 | snp | A/C | 3.43159e-05 | 0.00414207 | intron-variant | ARNT | GRCh38.p7 | 1:150813362 | ACAGCAAGGAAGAAT[A/C]AACAACTCCAATCTA | 405 |
rs751374107 | snp | A/G | 3.31774e-05 | 0.00407279 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836446 | TGTCTCACATGAGAC[A/G]ATAAACAGAAAGCCA | 405 |
rs751427271 | snp | C/T | 0.000103652 | 0.00719828 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817983 | GGACCTAGTTGTGGC[C/T]TCTGGATTGTGTTGG | 405 |
rs751549820 | snp | A/G | 1.73255e-05 | 0.0029432 | stop-gained | ARNT | GRCh38.p7 | 1:150839626 | TCATCTTGTTCCGTC[A/G]CCGCCGTTCAATTTC | 405 |
rs751550294 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150867767 | AGGTTTAGCACCATT[-/C]CCCTAATGCTCTCTC | 405 |
rs751562607 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150874461 | GAGACTGAGGCAAGG[A/C]TTGCTTGAGACCAGG | 405 |
rs751597630 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150830081 | ACCTATTTATGGGCC[A/C]GGCACCGTGGCTGAC | 405 |
rs751614572 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150852344 | AAAAAATTCAGTCTG[G/T]CCTCCTTGAGGATAA | 405 |
rs751627205 | snp | A/G | 6.61627e-05 | 0.00575126 | intron-variant | ARNT | GRCh38.p7 | 1:150852753 | AAGGAAAGTTTTTCA[A/G]TCTCTTACCTCAAAA | 405 |
rs751673284 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150847052 | TCGACCTCTTATCTA[C/T]TGCGCAAAATGGGCC | 405 |
rs751680564 | snp | A/G | 1.75072e-05 | 0.00295859 | intron-variant | ARNT | GRCh38.p7 | 1:150852860 | TAATACAAAACATTA[A/G]GAAGTTAAAATTTCT | 405 |
rs751684234 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865046 | AAAATATAAATTAAA[A/T]TTAATCTGACAGATT | 405 |
rs751702573 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150862967 | GAGGCAGAAGAATCG[A/C]TTGAACACAAAAGGC | 405 |
rs751739535 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150823077 | ACATGCCACCACGCC[C/T]GGCTAAATTTTTGTG | 405 |
rs751777201 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820196 | CCTAAAATATTTACT[A/G]TCTAGCCCCACTTAT | 405 |
rs751836435 | in-del | -/CAAA | 1.64933e-05 | 0.00287165 | intron-variant | ARNT | GRCh38.p7 | 1:150816209 | ATACGGAAAAAAGCC[-/CAAA]CAAACAAAAAATAAT | 405 |
rs751844167 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150867091 | ACACTGTAGTCCCAG[A/C]TACTCGAGAGGCTGA | 405 |
rs751866563 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809668 | AAAAGTTGCTAATGA[A/C]CCAACATAGTCTCCT | 405 |
rs751875276 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846021 | AACCTTGCAAGCACA[C/T]TGCTTTAGTTATCAC | 405 |
rs751890561 | snp | A/C | | | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861276 | ACTCGGGGTCTGAGG[A/C]AGGAGAATCTTGAGT | 405 |
rs751895417 | snp | C/T | 3.35503e-05 | 0.00409561 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836470 | AAAGCCATCTGCTGC[C/T]TCCAAGATCAAATGT | 405 |
rs751934130 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ARNT | GRCh38.p7 | 1:150839487 | CCATCAGTGGATGTG[C/T]TGCCAGTTCCCCGCA | 405 |
rs751977245 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150834861 | AGGCAGCATTGAAAA[C/T]AACATTGTGCAAGGA | 405 |
rs751983094 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150855656 | TCTGTAATCCCAACA[C/G]TTTAGGACGTCGAGA | 405 |
rs752056839 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150850432 | GATTGCAGTCGCGCG[A/C]CGCCACGCCTGACTG | 405 |
rs752088370 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | ARNT | GRCh38.p7 | 1:150816297 | TAGTAGGGGTCCAAG[C/T]TGGGGTTGCTCCTTG | 405 |
rs752090843 | snp | C/T | 8.55483e-05 | 0.00653964 | intron-variant | ARNT | GRCh38.p7 | 1:150830010 | CGTTAAAAGGTTTAA[C/T]GGGGACCTCCAACTC | 405 |
rs752095926 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150844547 | AGGAGCATCAGCAAC[A/G]AACAAATACTAAGTG | 405 |
rs752112004 | in-del | AAAAAAAAAAAAA/CACAC | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809636 | CACACACACACACAA[AAAAAAAAAAAAA/CACAC]AAAAAAAGTTGCTAA | 405 |
rs752127709 | in-del | -/AC | | | intron-variant | ARNT | GRCh38.p7 | 1:150866700 | CACACATACATATAC[-/AC]ACACACACACACGTA | 405 |
rs752135364 | snp | C/G | 1.65386e-05 | 0.00287559 | missense | ARNT | GRCh38.p7 | 1:150826559 | TGTTGGAAGCTGTCT[C/G]TTAGAAGCTGCTGGT | 405 |
rs752199019 | snp | A/C | 2.92282e-05 | 0.00382273 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858466 | GATGTCATTTCTGTC[A/C]GGAAAATAATGAAGT | 405 |
rs752240464 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150875961 | CAAGATCTAAGTTTC[A/G]AAGTATAGTCCGGGG | 405 |
rs752255096 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150822651 | TTTGTAATATCCTTT[A/C]TAATAAACTGGTAAA | 405 |
rs752265906 | snp | C/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877452 | GTCCCTGGTGAAAAA[C/G]TTAAATGACTAACTT | 405 |
rs752306018 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861155 | ACCCTTATGCACTGC[C/T]AGTGGAAATGTAAAA | 405 |
rs752325463 | in-del | -/CT | | | intron-variant | ARNT | GRCh38.p7 | 1:150820908 | TAGGGGCACTGACCC[-/CT]GTGCCATCGAAAATT | 405 |
rs752327066 | snp | G/T | 3.44596e-05 | 0.00415074 | intron-variant | ARNT | GRCh38.p7 | 1:150812120 | CATCTCCTGATAAAA[G/T]AAAAAGATTAAGTTT | 405 |
rs752373458 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant | ARNT | GRCh38.p7 | 1:150817343 | CCTACCCTCTTCAAC[A/G]AAGAGGACACAACTC | 405 |
rs752400225 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150841544 | ACCCAGATTAAAGAG[G/T]AAATAGTAGAAAAAA | 405 |
rs752423355 | in-del | -/A | 0.291392 | 0.24655 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876595 | CACCGCCGCCGCGCC[-/A]CCCCCCCCCCCAGTG | 405 |
rs752428543 | snp | A/T | 0.0002297 | 0.0107144 | intron-variant | ARNT | GRCh38.p7 | 1:150861338 | ACATCGCAAAAAAAA[A/T]ATTAAATTAAAAATA | 405 |
rs752440669 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846064 | ACACTGTATAAAATA[C/T]ACCGCCAGTTTGAAG | 405 |
rs752462701 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849891 | CTAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 405 |
rs752470113 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838034 | ACTAATTAAGTAGTC[-/G]CCCTGCTTTCAATCA | 405 |
rs752498902 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150833117 | ATGTAGTCATGTAAT[C/T]ATCCAAGGTTTCAGA | 405 |
rs752526390 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865639 | AGATTTACTCTCTGG[A/T]GAGTATAAATCAAAG | 405 |
rs752600161 | snp | C/T | 6.65148e-05 | 0.00576654 | intron-variant | ARNT | GRCh38.p7 | 1:150814251 | CCTGCTAAAGAGAGA[C/T]GGAGAGGGGATATAG | 405 |
rs752638460 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868189 | GCCGGGCACTGTGGT[A/G]TACACTTGTAATCCC | 405 |
rs752712524 | snp | A/C | 1.94426e-05 | 0.00311784 | intron-variant | ARNT | GRCh38.p7 | 1:150829567 | TGAAAAAATCAAAAT[A/C]ATTCCACTTTTCTAT | 405 |
rs752713563 | snp | A/G | 1.79149e-05 | 0.00299285 | intron-variant | ARNT | GRCh38.p7 | 1:150846224 | TCTACAACATGGATC[A/G]TATTATATATTACAA | 405 |
rs752770827 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150819531 | TGTCCATTAACGAAC[A/G]TACAGACAGTATGTG | 405 |
rs752773865 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150827258 | ATTTATAGTTGTGCA[A/G]TGATTACCACAATCC | 405 |
rs752795962 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865679 | TCTAGTGAACACGAC[A/G]TAAAGGTGAAAGTGA | 405 |
rs752808772 | snp | A/G | 3.54654e-05 | 0.00421087 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858337 | TTCATAACACACTAC[A/G]CTCAAACTCACCCTG | 405 |
rs752813303 | snp | A/G | 1.64898e-05 | 0.00287135 | intron-variant | ARNT | GRCh38.p7 | 1:150834662 | GAAGATGTGAAGAGC[A/G]GTCTGGAGTGCATTT | 405 |
rs752882120 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857908 | GGAATTTAATAAATA[C/T]TTTTGGAGCTGAATG | 405 |
rs752903648 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150843787 | CATGGTGGCTATGCA[C/T]ATAATCCCAAAAGTT | 405 |
rs752940310 | snp | C/T | 1.78039e-05 | 0.00298356 | synonymous-codon, intron-variant | ARNT | GRCh38.p7 | 1:150818003 | GATTGTGTTGGAGAG[C/T]GTAGGCCGTGGTTCT | 405 |
rs752944376 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858789 | ACCACACCCAGTTAA[-/T]TTTTTTTTTTTTTTT | 405 |
rs752945065 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ARNT | GRCh38.p7 | 1:150839529 | TGAGAAACTGCCATG[C/T]GTAAGATGGTTAGCT | 405 |
rs752985785 | in-del | -/CAGAG | | | intron-variant | ARNT | GRCh38.p7 | 1:150815845 | CTCTAGCCTGGGCGA[-/CAGAG]CAAGACTCTGTCTCA | 405 |
rs753020470 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150837698 | CCATATTCACTCTTC[C/T]CCACTACGAAATAAT | 405 |
rs753023322 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150818664 | ACAGATGGGAGGATT[A/G]CTTGAGCCTGGGAGG | 405 |
rs753038217 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875929 | CAGCAGGCAAAGACC[A/T]ACAGGCCCTCTTAAC | 405 |
rs753040360 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856163 | AAAGAAATATGGGCC[A/G]GGTGCAGTGGCTCGT | 405 |
rs753049853 | snp | A/T | 1.65449e-05 | 0.00287614 | missense | ARNT | GRCh38.p7 | 1:150826571 | TCTCTTAGAAGCTGC[A/T]GGTCTTCAGGATGAC | 405 |
rs753072150 | snp | C/T | 1.65433e-05 | 0.002876 | missense | ARNT | GRCh38.p7 | 1:150829100 | CTCCTCACCTGTGGC[C/T]GGTAGCCAACAGTAG | 405 |
rs753136169 | in-del | -/G | 1.65048e-05 | 0.00287265 | intron-variant | ARNT | GRCh38.p7 | 1:150817048 | GTAAGTGATCTAAAT[-/G]AGAATTTAAAAGGAT | 405 |
rs753149410 | snp | A/C | 1.7765e-05 | 0.0029803 | intron-variant | ARNT | GRCh38.p7 | 1:150852869 | ACATTAAGAAGTTAA[A/C]ATTTCTCAACACAAG | 405 |
rs753179846 | snp | C/G | 1.73015e-05 | 0.00294116 | intron-variant | ARNT | GRCh38.p7 | 1:150816441 | GTAAAAGATTAAAAG[C/G]ATAGATTTATCACAG | 405 |
rs753196380 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854143 | CAGGCTGGAGTACAG[A/T]GGCATGATCATAGCT | 405 |
rs753219965 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150872508 | CAAAAAGAATTCTCT[A/G]CTAATGAGAATACCA | 405 |
rs753232906 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150829634 | CTTCTTTTGTATAGG[A/G]GCAAAGGAAATTAAC | 405 |
rs753250713 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150859120 | TGGGTTTATACATTT[A/C]ATTCATGCAACAAAT | 405 |
rs753334631 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | ARNT | GRCh38.p7 | 1:150817371 | CTCACCTGGGAATGA[C/T]TGTAGCTGGCCAGTC | 405 |
rs753339451 | snp | C/T | 1.90965e-05 | 0.00308997 | intron-variant | ARNT | GRCh38.p7 | 1:150876502 | TGTCAGCCCCTTCGG[C/T]CCCTCCCCTTTAGAG | 405 |
rs753348131 | snp | C/T | 1.64857e-05 | 0.00287099 | missense | ARNT | GRCh38.p7 | 1:150813236 | TGTTGCTCACTAGAA[C/T]TTGAACGATGATGAG | 405 |
rs753394420 | snp | A/C/T | 7.99784e-05 | 0.00632329 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876603 | CCGCGCCACCCCCCC[A/C/T]CCCAGTGGGAGGAGC | 405 |
rs753397509 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838034 | ACTAATTAAGTAGTC[A/G]CCCTGCTTTCAATCA | 405 |
rs753397880 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150850178 | GGATCACGAGGTCAA[A/G]AGATCGAGACCATCC | 405 |
rs753495384 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150875249 | CGATTAATTTTACCT[A/C]CCTTTCCTTCAAAAA | 405 |
rs753495822 | snp | A/G | 1.65477e-05 | 0.00287638 | stop-gained | ARNT | GRCh38.p7 | 1:150813312 | TCCGTGTCTGGAATT[A/G]TCCTGCAGTCTGTCC | 405 |
rs753550666 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150839246 | ATTAATACTTATTAG[C/T]TTATTAAATAGTTTT | 405 |
rs753553254 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150874099 | GAAATAGGCATGGTG[A/T]CCCTAGTCCTTAAAA | 405 |
rs753556156 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839453 | GACCTGATCAGTGAG[A/G]AAAGACGGCTTATAG | 405 |
rs753568830 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863892 | TCTAAAGGGAGATAT[A/G]AAAATACAGTTATGT | 405 |
rs753572945 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150823599 | TCTGTCGCCCAGGCT[C/G]GAGTGCAGTGGCACG | 405 |
rs753582088 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816434 | AAATGAGGTAAAAGA[G/T]TAAAAGGATAGATTT | 405 |
rs753587106 | snp | C/T | 4.94214e-05 | 0.00497074 | missense | ARNT | GRCh38.p7 | 1:150816278 | GCAGAAAAGCCTGAG[C/T]GGGTAGTAGGGGTCC | 405 |
rs753647675 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867529 | GTCTCAACTTTAAAA[G/T]AAAAAGAGAGAGATA | 405 |
rs753670643 | snp | A/G | 3.57098e-05 | 0.00422536 | intron-variant | ARNT | GRCh38.p7 | 1:150846231 | CATGGATCATATTAT[A/G]TATTACAATATATTA | 405 |
rs753685920 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868090 | AATTGAAGTAGGAAG[A/G]CAAGCAGCTAGAAAG | 405 |
rs753702270 | snp | A/G | 1.68187e-05 | 0.00289984 | intron-variant | ARNT | GRCh38.p7 | 1:150846342 | TTGTTTCAAAGCATT[A/G]CACTTGTTATATCTA | 405 |
rs753728230 | snp | C/G | 1.76714e-05 | 0.00297244 | intron-variant | ARNT | GRCh38.p7 | 1:150830031 | CCTCCAACTCAAATG[C/G]CTTCAAAACTCAGAC | 405 |
rs753741524 | in-del | -/GA | | | intron-variant | ARNT | GRCh38.p7 | 1:150840686 | TGGAGGAGTGGAATG[-/GA]GAGGAGGATGATTAA | 405 |
rs753764198 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835746 | GAATAGATATGACTT[A/G]TTTCCTCTAGCCAAA | 405 |
rs753803500 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150812273 | TGACTCCTTTAGATC[G/T]CAGCCTTTTTTCCTA | 405 |
rs753839987 | snp | A/G | 1.64871e-05 | 0.00287111 | missense | ARNT | GRCh38.p7 | 1:150817192 | CCTGTGGTTGTCACA[A/G]GCTGAACCACCTGTG | 405 |
rs753853135 | snp | C/G | 4.95364e-05 | 0.00497652 | missense | ARNT | GRCh38.p7 | 1:150831893 | CATCCTTTACAGAGC[C/G]AAGTCCATTCCTAGA | 405 |
rs753890170 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820835 | ACATTAGAAATCCCA[A/G]CATTGGAAAATGCCT | 405 |
rs753893261 | snp | A/C | 1.65105e-05 | 0.00287315 | missense | ARNT | GRCh38.p7 | 1:150836318 | GAAAGCTGCTCACGA[A/C]GTTTATCCACATCAT | 405 |
rs753981966 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823223 | GGTACAGATGATGTA[C/T]TCAATTTCATCTGAG | 405 |
rs754020753 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150818081 | AGAGGGAGGAAGGGG[A/G]GAGAGAGAGAGAAAG | 405 |
rs754034501 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150817514 | AGAAAGAACCTTAAA[A/G]CAAATTAAACAGGCC | 405 |
rs754044365 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861725 | CCCAGCCAGGGTTTC[A/G]GTAATTTTTACCCAA | 405 |
rs754047400 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813161 | TTTTGAAAGTCTTTT[C/T]ACTCTCTTACCTGGA | 405 |
rs754122594 | snp | C/T | | | missense, splice-acceptor-variant | ARNT | GRCh38.p7 | 1:150816401 | GGAGGGGCTAGGCCA[C/T]TATTCCTAGGAGTGA | 405 |
rs754124424 | snp | A/G | 6.60077e-05 | 0.00574452 | intron-variant | ARNT | GRCh38.p7 | 1:150834684 | AGTGCATTTTTGTGT[A/G]TGGGGAAGAGGGGGA | 405 |
rs754145706 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878095 | TCAAGCAGTTATCCT[A/G]CCTCAGCCTCCTGAG | 405 |
rs754175963 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150872139 | TTTTTTGTATTTTTT[A/G]TAGTAAAGGGGTTTC | 405 |
rs754195399 | in-del | -/A | 5.05472e-05 | 0.00502703 | intron-variant | ARNT | GRCh38.p7 | 1:150817467 | TGACAAGACAAATAG[-/A]AAAAAAAAATTTTTT | 405 |
rs754211375 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870131 | TCTCTAACTTCTAGT[A/T]GCTATGTGACTTCAG | 405 |
rs754299833 | snp | A/G | 2.80682e-05 | 0.00374611 | stop-gained, synonymous-codon, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858356 | AAACTCACCCTGGTC[A/G]CCGCTTAATAGCCCT | 405 |
rs754317482 | snp | A/C | 1.66952e-05 | 0.00288917 | intron-variant | ARNT | GRCh38.p7 | 1:150826629 | GTTCCTAGAATACAG[A/C]AAGAAGAGTAAGATA | 405 |
rs754330066 | snp | G/T | 1.64961e-05 | 0.00287189 | intron-variant | ARNT | GRCh38.p7 | 1:150834677 | AGTCTGGAGTGCATT[G/T]TTGTGTGTGGGGAAG | 405 |
rs754342606 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845647 | GGTGGCTCACACCTA[C/T]AATCCCAGCACTTTG | 405 |
rs754378263 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150826409 | AGTCCTTTTCTATTC[C/T]TTAAAAATGCAGATT | 405 |
rs754389024 | in-del | -/G | 4.47838e-05 | 0.0047318 | intron-variant | ARNT | GRCh38.p7 | 1:150831925 | GAGTTACAGGAGTTT[-/G]AAAAAAAAAAAAAAA | 405 |
rs754424632 | snp | C/G | 2.33669e-05 | 0.00341803 | missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858433 | GAGGCAATGGCTGGA[C/G]CCAGTGATGGTACAT | 405 |
rs754442998 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150818662 | AGACAGATGGGAGGA[C/T]TGCTTGAGCCTGGGA | 405 |
rs754453492 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon | ARNT | GRCh38.p7 | 1:150816841 | GTTGCCCTGGGAGAA[C/T]AGCTGTTGGGTGGCA | 405 |
rs754467339 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150843341 | GTGTCAGGAATGTGT[C/T]AATTCCATTTTAAAT | 405 |
rs754478895 | snp | A/C | 1.92424e-05 | 0.00310175 | intron-variant | ARNT | GRCh38.p7 | 1:150829562 | ACTTATGAAAAAATC[A/C]AAATAATTCCACTTT | 405 |
rs754499936 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838089 | ATACATTTTTTATGT[C/T]TCCCCACTGCATAAA | 405 |
rs754504301 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820925 | GTGCCATCGAAAATT[C/T]GACTGTAAACTTCTG | 405 |
rs754572645 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150832157 | TCAAGAGAAGTTTTA[G/T]AAGTTTAGGAAAATA | 405 |
rs754574747 | snp | A/G | 1.64942e-05 | 0.00287173 | intron-variant | ARNT | GRCh38.p7 | 1:150817071 | AAAAGGATAATGAGA[A/G]AGAAACATACCCGCA | 405 |
rs754603094 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, synonymous-codon, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858379 | ATAGCCCTCTGGACA[A/G]TGGCTCCTCCACCTT | 405 |
rs754608735 | in-del | -/TT | | | intron-variant | ARNT | GRCh38.p7 | 1:150828352 | TGGTTTTTTTTTTGT[-/TT]TTTTTTTTTTTTGCA | 405 |
rs754622824 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150819527 | CAAATGTCCATTAAC[A/G]AACATACAGACAGTA | 405 |
rs754626170 | snp | A/G | 1.80439e-05 | 0.0030036 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811970 | AGATTTGCTTTTTAA[A/G]AACAAACAGTGATTT | 405 |
rs754657234 | snp | A/G | 2.54217e-05 | 0.00356514 | missense, utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858452 | GTGATGGTACATCTG[A/G]TGTCATTTCTGTCAG | 405 |
rs754694966 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150836938 | AGGTGTGGTGGCACA[C/T]GCCTGTAGTCCCAGC | 405 |
rs754698911 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871295 | ATTAGGCAGTCGTGG[-/T]TTTTTTTTTTTTTTT | 405 |
rs754699836 | snp | C/T | 1.72928e-05 | 0.00294043 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817984 | GACCTAGTTGTGGCC[C/T]CTGGATTGTGTTGGA | 405 |
rs754752690 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150823757 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTTG | 405 |
rs754758990 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150849144 | GGAGGCAGAGGTTGC[A/G]GTGAGCCGAGATCAT | 405 |
rs754769226 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150836007 | TTTAGAACGGAAAAA[A/G]AAAAGTATTGTAGGT | 405 |
rs754791751 | in-del | -/TGCT | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809309 | CTGGATTTTAAGAGC[-/TGCT]TGCTAACAGGCTAGG | 405 |
rs754795169 | snp | A/G | 3.43242e-05 | 0.00414257 | intron-variant | ARNT | GRCh38.p7 | 1:150813364 | AGCAAGGAAGAATAA[A/G]CAACTCCAATCTACA | 405 |
rs754806488 | snp | G/T | 2.21904e-05 | 0.00333087 | intron-variant | ARNT | GRCh38.p7 | 1:150839662 | GATTTTCCCTGCATG[G/T]AAAGAAAGAGAAGCC | 405 |
rs754813747 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150847913 | AGAGTATTTGGCAAA[A/G]TTCATCTAGTGAGTA | 405 |
rs754824680 | snp | A/G/T | 6.59408e-05 | 0.00574168 | missense | ARNT | GRCh38.p7 | 1:150814092 | CAAAGTTAGATCCAC[A/G/T]ATTGGTGAGACTAGG | 405 |
rs754844666 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820419 | TGTGATCCTAGCACT[G/T]TGGGAGGACGATGGA | 405 |
rs754874957 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860933 | AAGCAAACCCAATTT[C/T]AAAATGGGCAAAGAA | 405 |
rs754926130 | snp | C/T | 1.64871e-05 | 0.00287111 | missense | ARNT | GRCh38.p7 | 1:150829149 | CAAAAGTGAAGATAC[C/T]CTCAATGTTGTGTCG | 405 |
rs754937611 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846109 | CATAAATGATAGTTA[C/T]AATACTAAGTTTCAC | 405 |
rs755002645 | snp | C/G | 1.66233e-05 | 0.00288295 | intron-variant | ARNT | GRCh38.p7 | 1:150842414 | ATGCTAAAAGACACT[C/G]TTCTCCTACCTGGCA | 405 |
rs755025463 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150821918 | CTCAAGTGATCTGCT[C/G]AACTTGGTATCCCAA | 405 |
rs755027491 | snp | A/G/T | 0.000190148 | 0.00974887 | intron-variant | ARNT | GRCh38.p7 | 1:150831949 | AAAAAAAATCTACCC[A/G/T]TAAAACTCAAAGGGC | 405 |
rs755029474 | snp | A/T | 1.75277e-05 | 0.00296033 | intron-variant | ARNT | GRCh38.p7 | 1:150852862 | ATACAAAACATTAAG[A/T]AGTTAAAATTTCTCA | 405 |
rs755059776 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150825444 | TACAAAGTAAAAACC[A/G]TTATCAAAAGCCATG | 405 |
rs755090857 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825920 | ATTTTCTTTTTTATC[-/T]TTTTTTTTTTTGAGA | 405 |
rs755091822 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854426 | AACCAGGCATGGTGG[C/T]GCATGTGTAGTCCTA | 405 |
rs755094071 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150812383 | TTGCTGTATTTCATA[G/T]AACCCCCTATAGACA | 405 |
rs755151248 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863485 | ATAAAGAAGGCAGGC[A/G]ACCAGCCCATGGGGA | 405 |
rs755152317 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | ARNT | GRCh38.p7 | 1:150832390 | TGGGTCCACAGAGCT[A/C]CTGCCACACCTGTTT | 405 |
rs755183928 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852038 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 405 |
rs755239773 | snp | A/T | 0.000394252 | 0.0140346 | intron-variant | ARNT | GRCh38.p7 | 1:150817486 | AAAAAATTTTTTTTA[A/T]AAAAGAATCTGGAGA | 405 |
rs755353089 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150843849 | TATATCCCAAGGAGG[A/G]TATGTGAGGGGCACT | 405 |
rs755359912 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878117 | CCTCCTGAGTAGCTG[A/G]GATTACAGGCGCGCA | 405 |
rs755362112 | snp | A/C | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811832 | CTTGGAGATTCATTC[A/C]ATTTCTTCTATAAAT | 405 |
rs755373137 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872455 | ATTACCCTTTTCCTT[C/T]TACATTCTTCATCCA | 405 |
rs755379548 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810762 | GTTGAGATGGGTGTC[C/T]AGGCCCCATCTATCA | 405 |
rs755385525 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150840611 | AAACTTCTTACAAGA[A/C]TTAAGATACACCATC | 405 |
rs755417816 | snp | A/C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868493 | ATGGAGTATCAAGAA[A/C/T]TTGTAGAGGATTCTA | 405 |
rs755479056 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863221 | ACAAAAATTAGTCAG[C/G]TGTGGTGGTACACGT | 405 |
rs755493789 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870138 | CTTCTAGTAGCTATG[C/T]GACTTCAGACAAGTT | 405 |
rs755501847 | snp | C/T | 1.65408e-05 | 0.00287578 | synonymous-codon | ARNT | GRCh38.p7 | 1:150826567 | GCTGTCTCTTAGAAG[C/T]TGCTGGTCTTCAGGA | 405 |
rs755503741 | snp | C/T | 3.29516e-05 | 0.00405891 | missense | ARNT | GRCh38.p7 | 1:150816306 | TCCAAGTTGGGGTTG[C/T]TCCTTGGGTGGGGTT | 405 |
rs755548248 | snp | C/T | 1.65397e-05 | 0.00287569 | intron-variant | ARNT | GRCh38.p7 | 1:150852754 | AGGAAAGTTTTTCAG[C/T]CTCTTACCTCAAAAA | 405 |
rs755557009 | snp | A/T | 1.72249e-05 | 0.00293465 | intron-variant | ARNT | GRCh38.p7 | 1:150816437 | TGAGGTAAAAGATTA[A/T]AAGGATAGATTTATC | 405 |
rs755602809 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824160 | ACTCAAGCTTTCTTA[-/T]TAGGTTGGTGCAAAA | 405 |
rs755618528 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | ARNT | GRCh38.p7 | 1:150817180 | CTGTGTTCTGGTCCT[A/G]TGGTTGTCACAGGCT | 405 |
rs755625104 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854135 | CTGTTACTCAGGCTG[A/G]AGTACAGTGGCATGA | 405 |
rs755657514 | snp | A/G | 0.00191433 | 0.0308788 | intron-variant | ARNT | GRCh38.p7 | 1:150861339 | CATCGCAAAAAAAAA[A/G]TTAAATTAAAAATAG | 405 |
rs755659506 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150869543 | TTTTAGGAAACTACT[C/T]CTTTTTTTTTTTTTT | 405 |
rs755673704 | snp | G/T | 3.30579e-05 | 0.00406544 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858467 | ATGTCATTTCTGTCA[G/T]GAAAATAATGAAGTA | 405 |
rs755674534 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150835670 | TATTGAAATTTCTTG[A/C]ATTTTAACTACCAGT | 405 |
rs755683776 | in-del | -/T | 5.25831e-05 | 0.00512726 | intron-variant | ARNT | GRCh38.p7 | 1:150831933 | GAGTTTGAAAAAAAA[-/T]AAAAAAAATCTACCC | 405 |
rs755691237 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150825389 | CATTGTATCAATAAC[A/G]ACACTACTGAGACTT | 405 |
rs755718188 | snp | A/T | 1.72561e-05 | 0.0029373 | intron-variant | ARNT | GRCh38.p7 | 1:150812122 | TCTCCTGATAAAAGA[A/T]AAAGATTAAGTTTGG | 405 |
rs755723905 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150839706 | CACATCTGGTCATTT[A/G]GTAGCAGGGAGAGTG | 405 |
rs755726605 | snp | C/T | 8.2603e-05 | 0.00642609 | missense | ARNT | GRCh38.p7 | 1:150836378 | CCAAACCATTCAGAC[C/T]GTGGCTGGTTCAAAA | 405 |
rs755753589 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150872013 | CCAGGCTGGAGTACA[A/G]TGGCATGATCACAGC | 405 |
rs755762181 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150832046 | CACCCAAAAATGACC[A/G]CCACATTTTTACCCT | 405 |
rs755780418 | snp | C/T | 3.71078e-05 | 0.00430726 | intron-variant | ARNT | GRCh38.p7 | 1:150836497 | ATGTTTCAGTTCCTG[C/T]GCAAGAAAAAGAAAT | 405 |
rs755820540 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852604 | TCTAGAGATATTAAC[A/G]GAATGCTTAAAAATT | 405 |
rs755902371 | snp | A/C/G | 1.66763e-05 | 0.00288753 | intron-variant | ARNT | GRCh38.p7 | 1:150814256 | TAAAGAGAGATGGAG[A/C/G]GGGGATATAGAACAA | 405 |
rs755913469 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820233 | AGCTTGCCTACCCCT[A/G]CTCCAGAGGAAAATC | 405 |
rs755938379 | snp | C/T | 0.000133023 | 0.00815437 | intron-variant | ARNT | GRCh38.p7 | 1:150829577 | AAAATAATTCCACTT[C/T]TCTATTGTTAGTCAG | 405 |
rs755941201 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865870 | AGGGTGTAAGAAATG[C/T]CTTGGATGTATGAAA | 405 |
rs756047101 | snp | C/T | 1.78828e-05 | 0.00299017 | intron-variant | ARNT | GRCh38.p7 | 1:150846228 | CAACATGGATCATAT[C/T]ATATATTACAATATA | 405 |
rs756069924 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863969 | ATTTCAACATTGTGT[A/G]AATATCATTGAGTAT | 405 |
rs756122904 | snp | C/T | 1.64912e-05 | 0.00287147 | intron-variant | ARNT | GRCh38.p7 | 1:150834665 | GATGTGAAGAGCAGT[C/T]TGGAGTGCATTTTTG | 405 |
rs756151126 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824594 | GAGTAGCTGGGGACT[A/T]GAGGCGTGCACCATC | 405 |
rs756164238 | snp | C/G/T | 3.25008e-05 | 0.00403105 | intron-variant | ARNT | GRCh38.p7 | 1:150817877 | TGCAAATGACCACCC[C/G/T]CTGGGTGACTGCTCA | 405 |
rs756204098 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150827390 | TGCCTCTCTAGTTCT[A/G]CTATTTCTACAAATT | 405 |
rs756216042 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845036 | GCTGGTTTTGAACTC[C/T]TGACCTCAAGTGATC | 405 |
rs756267241 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810016 | TTAAACTATAGATTC[C/T]TCTGGTTGTGGGTGC | 405 |
rs756290690 | snp | C/T | 5.35748e-05 | 0.00517538 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150818005 | TTGTGTTGGAGAGTG[C/T]AGGCCGTGGTTCTTG | 405 |
rs756299824 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816217 | AAAAGCCCAAACAAA[C/T]AAAAAATAATACACA | 405 |
rs756301424 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859710 | ATATACCTAACTCTG[C/T]AATCAAAAAGAGGTG | 405 |
rs756301659 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878058 | TGCGATCTTGGCTCA[C/T]TGCAACCTCTCCCTC | 405 |
rs756316657 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813752 | TGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCGC | 405 |
rs756342019 | snp | G/T | 4.94434e-05 | 0.00497184 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814099 | AGATCCACGATTGGT[G/T]AGACTAGGGTAGGCA | 405 |
rs756354372 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150832671 | GATAGTACATATTTT[C/T]AGCTTTGCGGGCCAG | 405 |
rs756404492 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865357 | AAACTAGAGATAAAA[C/T]GGACTATTGCCTTGG | 405 |
rs756411577 | in-del | -/AG | 5.39408e-05 | 0.00519302 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811978 | TTTTTAAAAACAAAC[-/AG]TGATTTTTTCTCCCC | 405 |
rs756426374 | snp | A/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876950 | AATGACCGAGTAACG[A/T]CATTGAAATGCAATT | 405 |
rs756442951 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150869979 | AAAAAGACAATACTC[C/T]ACCTACCTCCTTCTC | 405 |
rs756473859 | snp | G/T | 0.000585671 | 0.0171024 | missense | ARNT | GRCh38.p7 | 1:150829103 | CTCACCTGTGGCTGG[G/T]AGCCAACAGTAGCCA | 405 |
rs756523269 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825151 | AGGCATGAGCGACCA[C/T]GCCCAGCCAATTTTA | 405 |
rs756563413 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150844370 | CCTTTAATCAATTCT[A/G]TAACTGCTACCAGAG | 405 |
rs756586173 | snp | C/T | 1.79877e-05 | 0.00299892 | intron-variant | ARNT | GRCh38.p7 | 1:150852874 | AAGAAGTTAAAATTT[C/T]TCAACACAAGCTACC | 405 |
rs756645493 | snp | C/T | 2.96802e-05 | 0.00385217 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858351 | CACTCAAACTCACCC[C/T]GGTCGCCGCTTAATA | 405 |
rs756666812 | in-del | -/AT | | | intron-variant | ARNT | GRCh38.p7 | 1:150813443 | TTAATTTTACCTAGG[-/AT]ATAACTCTGTCCTTC | 405 |
rs756714974 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150843442 | TTAGCTATTAAAAAT[C/G]ACAAATACAATAACC | 405 |
rs756789458 | snp | C/T | 3.2969e-05 | 0.00405998 | missense | ARNT | GRCh38.p7 | 1:150813237 | GTTGCTCACTAGAAC[C/T]TGAACGATGATGAGG | 405 |
rs756797721 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840438 | CTCCATAGCTGATAC[A/G]AGAATTGATAGTACA | 405 |
rs756826614 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827035 | TTAATCCTAAGATTA[C/T]AGTTAAGTGAGGAGG | 405 |
rs756869076 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823331 | AGACAGCACTTGGCC[C/T]TTTAATTTCACTACC | 405 |
rs756869617 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849543 | GTAATCCCAACACTT[G/T]GGAAGGCCAAGGTGG | 405 |
rs756880154 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150830641 | ATAGGCAGAAAATTT[A/C]TGCTTTGCCTAATCT | 405 |
rs756921349 | snp | A/G | 1.65745e-05 | 0.00287871 | synonymous-codon | ARNT | GRCh38.p7 | 1:150826588 | GTCTTCAGGATGACA[A/G]AATTCTACAATATTC | 405 |
rs756996050 | in-del | -/TTTTT/TTTTTT | | | intron-variant | ARNT | GRCh38.p7 | 1:150860218 | GAAAAAAAAAAATTC[-/TTTTT/TTTTTT]TTTTTTTTTTTTTTT | 405 |
rs757000860 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150818814 | TGGTAGGGAAAATGA[C/T]ACATAAACATGGAGA | 405 |
rs757035643 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150821258 | TCACCTTTTTCTTAT[-/A]ATGTCATGACTTTTC | 405 |
rs757044524 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150855398 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAT | 405 |
rs757098376 | snp | C/T | 5.32184e-05 | 0.00515814 | intron-variant | ARNT | GRCh38.p7 | 1:150830032 | CTCCAACTCAAATGC[C/T]TTCAAAACTCAGACA | 405 |
rs757165074 | snp | A/C | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878634 | TAAAATTTCATTTTT[A/C]TTTCATTTTGTTGTT | 405 |
rs757220963 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150827645 | TATGAACTGTGTACA[A/G]ATCTATGGGTGAACA | 405 |
rs757224887 | snp | A/G | 1.80078e-05 | 0.0030006 | intron-variant | ARNT | GRCh38.p7 | 1:150831918 | CCTAGAAGAGTTACA[A/G]GAGTTTGAAAAAAAA | 405 |
rs757224933 | snp | A/C/T | 4.94844e-05 | 0.00497395 | missense | ARNT | GRCh38.p7 | 1:150817199 | TTGTCACAGGCTGAA[A/C/T]CACCTGTGGAATACA | 405 |
rs757226269 | snp | C/T | 0.000115989 | 0.00761453 | intron-variant | ARNT | GRCh38.p7 | 1:150876503 | GTCAGCCCCTTCGGC[C/T]CCTCCCCTTTAGAGG | 405 |
rs757276657 | in-del | -/C | 0.0383776 | 0.133101 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876595 | ACCGCCGCCGCGCCA[-/C]CCCCCCCCCCCAGTG | 405 |
rs757304972 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856514 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 405 |
rs757331508 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150876449 | GCCCCGGCGCCTTCA[A/G]CTCCAGCTGCGTCCC | 405 |
rs757335397 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150867348 | CAGTCTGGGCAATAC[A/C]GTGAGACCTCATTTC | 405 |
rs757360009 | snp | A/G | 1.66441e-05 | 0.00288474 | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150842459 | CGCAGAGCTCTGCTC[A/G]TCATCCGACCTAAAA | 405 |
rs757408478 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813580 | CATACTATTAAATGT[A/T]TAAAAATTCACATGA | 405 |
rs757419882 | snp | C/T | 1.68709e-05 | 0.00290434 | intron-variant | ARNT | GRCh38.p7 | 1:150814275 | GATATAGAACAAATA[C/T]AGCATTAACATCATT | 405 |
rs757425930 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150874543 | ATTTAAAAATTAACC[A/G]CGCATGGTGGCAAGG | 405 |
rs757444128 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150830206 | CAAAAATTAGCCAGG[C/T]ATGGTGGCATGCACC | 405 |
rs757451897 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150828582 | TTCTCTTTGTTCTTT[A/G]TTTTCAAGACCTCTT | 405 |
rs757473181 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150847089 | CATGAGTGTGCAAAT[A/C]TCTCTTCAAGATTCT | 405 |
rs757487348 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150855919 | CCGAAATGTGTGTGT[A/G]TGTGTATTGCTTATT | 405 |
rs757498017 | snp | C/T | 1.67565e-05 | 0.00289447 | missense | ARNT | GRCh38.p7 | 1:150812070 | GGGAATTCTTCATTG[C/T]TGTAGCTGTTGCTCT | 405 |
rs757503041 | in-del | -/AA | 0.00171142 | 0.0292024 | intron-variant | ARNT | GRCh38.p7 | 1:150831926 | AGTTACAGGAGTTTG[-/AA]AAAAAAAAAAAAAAT | 405 |
rs757563399 | snp | A/G | 1.78153e-05 | 0.00298452 | intron-variant | ARNT | GRCh38.p7 | 1:150846233 | TGGATCATATTATAT[A/G]TTACAATATATTACC | 405 |
rs757588327 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150822948 | TTGAAATGGAGTCTC[A/G]CTCTGTAGCCCAGGC | 405 |
rs757608544 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809679 | ATGAACCAACATAGT[C/T]TCCTAGAGGGAAACC | 405 |
rs757612737 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840856 | CCATTAAGTTTCTCA[C/G]TGTCCTCCATGGGGA | 405 |
rs757632903 | snp | C/T | 1.65083e-05 | 0.00287296 | intron-variant | ARNT | GRCh38.p7 | 1:150817041 | CCCATCAGTAAGTGA[C/T]CTAAATGAGAATTTA | 405 |
rs757642476 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844657 | AAAAGAAATAATTTA[A/T]TGCCTAATATTTAAT | 405 |
rs757644937 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150813667 | TTATTTTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 405 |
rs757673511 | in-del | -/A | 5.05472e-05 | 0.00502703 | intron-variant | ARNT | GRCh38.p7 | 1:150817468 | TGACAAGACAAATAG[-/A]AAAAAAAATTTTTTT | 405 |
rs757676339 | snp | C/T | | | synonymous-codon | ARNT | GRCh38.p7 | 1:150839522 | CTTCATGTGAGAAAC[C/T]GCCATGCGTAAGATG | 405 |
rs757715657 | snp | C/T | 8.22944e-05 | 0.00641408 | missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858358 | ACTCACCCTGGTCGC[C/T]GCTTAATAGCCCTCT | 405 |
rs757734505 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859419 | TGGCATGATCATGGC[A/T]TACTGCAGCCTCAAC | 405 |
rs757766972 | snp | C/T | 1.65111e-05 | 0.0028732 | missense | ARNT | GRCh38.p7 | 1:150836322 | GCTGCTCACGAAGTT[C/T]ATCCACATCATCTGG | 405 |
rs757838496 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861321 | GGAAACACAGCAAGA[C/T]AACATCGCAAAAAAA | 405 |
rs757845103 | snp | C/T | 1.85634e-05 | 0.00304653 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150818017 | GTGTAGGCCGTGGTT[C/T]TTGGCTAGAGTTCCT | 405 |
rs757886398 | snp | C/G | 1.66194e-05 | 0.00288261 | synonymous-codon | ARNT | GRCh38.p7 | 1:150826612 | AATATTCTTTCCTAA[C/G]AGTTCCTAGAATACA | 405 |
rs757893924 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824194 | TTGCATTTTTTGCCA[-/T]TTTAAAAAAATGGCA | 405 |
rs757927865 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868297 | CTGTCTCAAAAAAGA[A/G]TCAAGACCCTGTCTC | 405 |
rs757951142 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809537 | TTGCTTGAACCCAAG[A/G]GGCAGAGGTTGCAGT | 405 |
rs758003019 | snp | A/G | 4.95037e-05 | 0.00497488 | missense | ARNT | GRCh38.p7 | 1:150829125 | CAGTAGCCACACAGC[A/G]GTGATCCACAAAAGT | 405 |
rs758015701 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150860006 | AGCAAGATCCTGTCT[-/A]AAAAAAAAAAAAGGG | 405 |
rs758076714 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150839335 | GAAATTCGTTTTCCC[A/G]TTGTCTGACTTCTTC | 405 |
rs758100528 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150821038 | TGTTGTACGTATTAT[A/G]TACTGTATTCTTACA | 405 |
rs758154335 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150816465 | ATCACAGAAGCTAGG[A/G]ATCAAAGGACAATCT | 405 |
rs758218827 | snp | G/T | 1.77237e-05 | 0.00297684 | intron-variant | ARNT | GRCh38.p7 | 1:150817479 | ATAGAAAAAAAAATT[G/T]TTTTTAAAAAAGAAT | 405 |
rs758221572 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866043 | GCTGGTGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 405 |
rs758232580 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817406 | TCTTCCTGGTACCAT[A/G]TCCAATTCTGTTTGC | 405 |
rs758268286 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150833134 | TCCAAGGTTTCAGAA[A/G]ATAGCATCAAAGCTA | 405 |
rs758270296 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819725 | TCTAGAATAGACAAA[C/T]TTATAAAGACAACAG | 405 |
rs758278667 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877335 | AGTGGTTGCCGTGCA[A/G]ACAATGTATCTTGTA | 405 |
rs758361425 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813250 | ACTTGAACGATGATG[A/G]GGCTGCTGGCCCTGC | 405 |
rs758393769 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150849295 | TTGGGCTCCTTTATC[A/C]AATTGTCTGTTACTC | 405 |
rs758403177 | snp | A/G/T | 0.000115316 | 0.00759258 | synonymous-codon | ARNT | GRCh38.p7 | 1:150816289 | TGAGCGGGTAGTAGG[A/G/T]GTCCAAGTTGGGGTT | 405 |
rs758410825 | snp | C/G/T | 5.13636e-05 | 0.0050675 | intron-variant | ARNT | GRCh38.p7 | 1:150813361 | TACAGCAAGGAAGAA[C/G/T]AAACAACTCCAATCT | 405 |
rs758478955 | snp | C/G | 0.000122845 | 0.00783628 | intron-variant | ARNT | GRCh38.p7 | 1:150831776 | GACTCTGTGAGGAAC[C/G]AACTGTACCAAGGGG | 405 |
rs758496050 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150871340 | GAGTCTCACTCTGTC[A/G]CCCAGGCTAGAGTGC | 405 |
rs758563752 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854618 | TCCCAGCACTTTGGG[A/G]AGCTGAGGCAGGCGG | 405 |
rs758580738 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150844287 | GTAACCCAGGCCCTC[A/C]TGATTTTATAGCTGT | 405 |
rs758606343 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150826872 | GGCTGGTCTCGAACT[C/T]CTGACCTCAAGTGAT | 405 |
rs758680158 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865722 | GAAAACAGGAAAACT[A/G]ACACCAATGTATGCA | 405 |
rs758700876 | snp | A/G | 0.000949938 | 0.0217731 | intron-variant | ARNT | GRCh38.p7 | 1:150831927 | GTTACAGGAGTTTGA[A/G]AAAAAAAAAAAAAAT | 405 |
rs758777469 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820988 | TGTTGGCCAGAAGCC[C/T]TACCAATAACATAAG | 405 |
rs758805880 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856370 | GCGTGAACCTGGGAG[A/G]TGGAGGTTACAGTGA | 405 |
rs758816624 | snp | C/G/T | 3.30356e-05 | 0.0040641 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836356 | CACCTGATCATAGAG[C/G/T]GTGCTGCCAAACCAT | 405 |
rs758832560 | in-del | -/TA | | | intron-variant | ARNT | GRCh38.p7 | 1:150836701 | TTTCCTCACTTTCTC[-/TA]TGTCACTATCCACCT | 405 |
rs758834473 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150876002 | GGACGGGGGTTGCGG[A/G]TGGGAGGTAACAGCC | 405 |
rs758856351 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150874444 | TGTATTCCCAACTTG[A/G]AGAGACTGAGGCAAG | 405 |
rs758910980 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150813536 | GGCAGCCTTTCCATA[A/G]AGTTCTTTACTCATT | 405 |
rs758930216 | snp | A/C | 6.72235e-05 | 0.00579717 | intron-variant | ARNT | GRCh38.p7 | 1:150823159 | TGTGAGAACAGAGGA[A/C]AAACAGTTTTTTCAC | 405 |
rs758932114 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150873381 | GGACCACCTACCCAC[C/T]GAGTTCTACTTGCCA | 405 |
rs758939638 | snp | A/G | 7.18739e-05 | 0.00599431 | intron-variant | ARNT | GRCh38.p7 | 1:150846214 | ACTGTCTGGTTCTAC[A/G]ACATGGATCATATTA | 405 |
rs758953521 | snp | A/T | 1.70799e-05 | 0.00292227 | intron-variant | ARNT | GRCh38.p7 | 1:150814285 | AAATACAGCATTAAC[A/T]TCATTGCACATACCA | 405 |
rs758956128 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant | ARNT | GRCh38.p7 | 1:150816246 | CAGGGAACACACAGA[C/T]GATAAGTTTTACCTG | 405 |
rs758985362 | snp | C/G | 1.64773e-05 | 0.00287026 | missense | ARNT | GRCh38.p7 | 1:150823307 | CTTAGACCGGAACCG[C/G]AACATGACAGACAGC | 405 |
rs759046875 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861000 | GGCCAATAAATACAT[A/G]TAAAGTGCTCAACAT | 405 |
rs759051846 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150839269 | ATAGTTTTCACAACT[C/G]TTCTCTACTTCTCAT | 405 |
rs759060615 | snp | C/T | 0.000100528 | 0.00708899 | intron-variant | ARNT | GRCh38.p7 | 1:150829990 | AAACACCTTCAGAAA[C/T]GTGACGTTAAAAGGT | 405 |
rs759068122 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828474 | TAAGAATAGACCTTA[C/T]TCTGGTCTATTGATC | 405 |
rs759100446 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150864311 | GTCATTAGGTGACAC[A/G]TAACAGCAACTGTGA | 405 |
rs759137535 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857989 | TTCTAGAGCTCAGCA[G/T]TCTCTAAATTCAGAA | 405 |
rs759149935 | in-del | -/T | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809289 | AAAAATACAGGCTTA[-/T]TGCCTCTGGATTTTA | 405 |
rs759150051 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815063 | CATGTTTGGATAATT[C/T]CTTCCAGTTTCTATT | 405 |
rs759158743 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813080 | CCCCAACCAAACACC[A/T]CAATCCAGGCATGCT | 405 |
rs759186863 | snp | A/C | 1.67245e-05 | 0.00289171 | intron-variant | ARNT | GRCh38.p7 | 1:150846311 | TCATCATCACACCTG[A/C]AGGAGAGAAAAAGGA | 405 |
rs759191655 | snp | A/G | 3.29674e-05 | 0.00405988 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817164 | CTTCTCAAGGGGCTT[A/G]CTGTGTTCTGGTCCT | 405 |
rs759195405 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150875240 | TAATTTTTGCGATTA[A/G]TTTTACCTCCCTTTC | 405 |
rs759220968 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875720 | CTGCACTACACCCTA[C/T]TCCATCTCTTAGACA | 405 |
rs759226567 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150849536 | CATGCCTGTAATCCC[A/C]ACACTTTGGAAGGCC | 405 |
rs759236107 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150843731 | TAAGCCACCACTCCC[A/G]GCCTCTTACTGTCAT | 405 |
rs759242068 | snp | C/T | 1.65312e-05 | 0.00287495 | missense | ARNT | GRCh38.p7 | 1:150831839 | GGGGCCAGGCCTTGA[C/T]GTAGCCTGTGCAGTG | 405 |
rs759294503 | snp | C/T | 1.65743e-05 | 0.00287869 | intron-variant | ARNT | GRCh38.p7 | 1:150836268 | TTCATTTCCCATACA[C/T]ATAACTCTCACCTGT | 405 |
rs759303852 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813112 | CCTTCACTGTCTCTC[C/T]TCCTCCTGGACCCTT | 405 |
rs759311210 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150831113 | TACCCTAGGTGATGC[C/T]ACTAATAAGTAACAA | 405 |
rs759326697 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845947 | TCTGTATTCCTATTT[C/T]TGTAGATCCATTTAA | 405 |
rs759359395 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838000 | TGCTTTGTCACTGTC[C/G]TAGTCATCTTTTACC | 405 |
rs759365127 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868928 | AATTTAAAAAAAAAA[A/G]GACCAGCCTGGGCAA | 405 |
rs759398102 | snp | C/G | 1.64906e-05 | 0.00287142 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823208 | CTTCACATTGGTGTT[C/G]GTACAGATGATGTAC | 405 |
rs759408168 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840684 | ACTGGAGGAGTGGAA[C/T]GGAGAGGAGGATGAT | 405 |
rs759411882 | in-del | -/TCAG | | | intron-variant | ARNT | GRCh38.p7 | 1:150866277 | CGTGAGCCACCAAGG[-/TCAG]TCAGCCTGTTCCAAG | 405 |
rs759423139 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150815409 | AAAAATTAGCCAGGC[A/G]TGGTGGCGAGCACCC | 405 |
rs759471197 | snp | C/G | 3.30715e-05 | 0.00406628 | intron-variant | ARNT | GRCh38.p7 | 1:150818077 | GTGGAGAGGGAGGAA[C/G]GGGGGAGAGAGAGAG | 405 |
rs759475110 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150851856 | CAAGAATGATCAATA[A/C]AAAAGAAAATTAATA | 405 |
rs759478913 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150824414 | TTGCTCTTCAATCCT[A/G]TTTTTTCCCCGAAAC | 405 |
rs759522563 | snp | A/G | 1.65671e-05 | 0.00287807 | intron-variant | ARNT | GRCh38.p7 | 1:150814243 | GGTAGCCACCTGCTA[A/G]AGAGAGATGGAGAGG | 405 |
rs759562100 | in-del | -/C | 1.73839e-05 | 0.00294816 | intron-variant | ARNT | GRCh38.p7 | 1:150816768 | GGCCCTGTAAAGCAG[-/C]ACATATATACGGGGC | 405 |
rs759621227 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150818526 | GAGGCTGAGGCAGGG[C/T]GGATTGCTTGAGCTC | 405 |
rs759659333 | snp | A/G | 1.67133e-05 | 0.00289074 | intron-variant | ARNT | GRCh38.p7 | 1:150829266 | AGGTAAAATGATACC[A/G]TTATTTACAGATGTA | 405 |
rs759664540 | in-del | -/GT | | | intron-variant | ARNT | GRCh38.p7 | 1:150868224 | ACTCAGGAAGCAGAG[-/GT]GGGAGGATCATTTGA | 405 |
rs759685196 | snp | A/G | 0.000100175 | 0.00707655 | missense | ARNT | GRCh38.p7 | 1:150816804 | TGAAATTCTCTGCCG[A/G]CCGGGGGGTAGGAGG | 405 |
rs759686761 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150818653 | ATACTCAGGAGACAG[A/T]TGGGAGGATTGCTTG | 405 |
rs759741689 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816909 | TGGACCAAAAGGAGT[C/T]GGGGAAGGGCCAGTC | 405 |
rs759758337 | in-del | -/GAA | 0.00163952 | 0.0285845 | intron-variant | ARNT | GRCh38.p7 | 1:150829236 | TAGTTACCTGAGAGT[-/GAA]GAGATAAAAATGAGG | 405 |
rs759762126 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150869753 | AGACAAGGTCTCCCT[A/G]TATTGCTCAGGCTGG | 405 |
rs759776156 | in-del | -/ACACATACAGAC | | | intron-variant | ARNT | GRCh38.p7 | 1:150834947 | GCTGATTATCTGTAT[-/ACACATACAGAC]ATACATACAGAGTAA | 405 |
rs759809720 | snp | C/T | 2.25289e-05 | 0.00335618 | missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858412 | ATTCCAGGTCCAGAG[C/T]TTCCAGAGGCAATGG | 405 |
rs759811682 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | ARNT | GRCh38.p7 | 1:150834652 | CGCCCTGAAGGAAGA[C/T]GTGAAGAGCAGTCTG | 405 |
rs759838372 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150874208 | ATTTCCACCTATGTC[C/T]CTCCATTCATTAATC | 405 |
rs759857728 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150867864 | TCCTGCCAGCCATGT[A/G]AAGACATGCTTGCTT | 405 |
rs759919140 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | ARNT | GRCh38.p7 | 1:150839521 | ACTTCATGTGAGAAA[C/T]TGCCATGCGTAAGAT | 405 |
rs759922275 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant | ARNT | GRCh38.p7 | 1:150839437 | AACTATAAGTCCCAG[A/G]GACCTGATCAGTGAG | 405 |
rs759972259 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150829592 | TTCTATTGTTAGTCA[C/G]GTAATGATACAATGA | 405 |
rs760026864 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150827660 | AATCTATGGGTGAAC[A/G]TGTTTTCATTTCTCT | 405 |
rs760047493 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150837575 | ACTCCAATTTTTGCT[C/T]CCTCTTCTGTTTCAG | 405 |
rs760070034 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860372 | AGGCACGCACCACCA[C/T]GCCTGGCTAATTTTT | 405 |
rs760094080 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150866842 | GTGATGAAAGATACA[C/G]AAAGGTAGGAAGAAC | 405 |
rs760135403 | snp | C/G | 1.65537e-05 | 0.0028769 | missense | ARNT | GRCh38.p7 | 1:150829098 | AGCTCCTCACCTGTG[C/G]CTGGTAGCCAACAGT | 405 |
rs760144690 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821736 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGT | 405 |
rs760161064 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150812908 | CAGGCTAGTTGCTCA[G/T]CCTGGCTTTGAACTC | 405 |
rs760199545 | snp | C/G | 1.64749e-05 | 0.00287005 | intron-variant | ARNT | GRCh38.p7 | 1:150817351 | CTTCAACGAAGAGGA[C/G]ACAACTCACCTGGGA | 405 |
rs760225190 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150855664 | CCCAACACTTTAGGA[C/T]GTCGAGATGGGAGGG | 405 |
rs760251073 | snp | A/G | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811666 | TTCCAAAAACAAGCC[A/G]TACTATCCAAGGCAA | 405 |
rs760264587 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827437 | ACATAATATGTGGTC[A/T]TTTGGGTCTGGCTTC | 405 |
rs760299312 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150839045 | CTTCTATCACCAAAG[A/G]TGGGACAGATTCATT | 405 |
rs760306490 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828973 | GGTACTAACAGAATA[C/T]GATGATCTCTTTTTC | 405 |
rs760346755 | in-del | -/AT | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811508 | CTCTCACTTACTCAC[-/AT]GTTTCTTTCCAGAGG | 405 |
rs760350263 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150849962 | GAGGCTGAGGCACTA[C/G]AATCGCTTGAACCTG | 405 |
rs760358269 | snp | C/G | 1.64754e-05 | 0.00287009 | intron-variant | ARNT | GRCh38.p7 | 1:150832325 | GGTTTTCACCACTTA[C/G]GATCTCACCTGCATC | 405 |
rs760384334 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | ARNT | GRCh38.p7 | 1:150817458 | AAAGGCCAGTTGACA[A/G]GACAAATAGAAAAAA | 405 |
rs760449401 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150867139 | AACCTAGGAGGCGGA[C/G]GCTGCGGTGAGCCAA | 405 |
rs760463448 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823220 | GTTGGTACAGATGAT[A/G]TACTCAATTTCATCT | 405 |
rs760479315 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150842896 | ACTGCTCCCAATCTG[A/G]AAAGAAAATGATATC | 405 |
rs760514784 | snp | A/C | 1.64746e-05 | 0.00287002 | missense | ARNT | GRCh38.p7 | 1:150816264 | TAAGTTTTACCTGGG[A/C]AGAAAAGCCTGAGCG | 405 |
rs760531583 | in-del | -/ACACAT/ACAT | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811473 | CACACACACACACAC[-/ACACAT/ACAT]ACACATACACACACA | 405 |
rs760538848 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857632 | ACCAAAAAGTAAATA[A/C]AATAGTGCCCATTCT | 405 |
rs760611662 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853609 | CTAATAAACATGTAA[C/T]ATATACTTCATTCAA | 405 |
rs760635188 | snp | G/T | 1.65241e-05 | 0.00287433 | missense | ARNT | GRCh38.p7 | 1:150816378 | CTGATGGCTGGACAA[G/T]GGTTACAGGAGGGGC | 405 |
rs760694753 | in-del | -/A | 0.000102723 | 0.00716596 | intron-variant | ARNT | GRCh38.p7 | 1:150852851 | GCCTGCTGATAATAC[-/A]AAACATTAAGAAGTT | 405 |
rs760704440 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871480 | TAATTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 405 |
rs760714433 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150837970 | TAATTCAGTTTTATC[A/G]ATTCTACTTTCCAAT | 405 |
rs760750995 | snp | C/G | 1.6804e-05 | 0.00289858 | intron-variant | ARNT | GRCh38.p7 | 1:150846337 | AAGGATTGTTTCAAA[C/G]CATTACACTTGTTAT | 405 |
rs760762958 | in-del | -/ATTATGGCT | | | intron-variant | ARNT | GRCh38.p7 | 1:150812544 | TTGTGTAAATAGACC[-/ATTATGGCT]ATAATCATTATGTTC | 405 |
rs760782153 | snp | A/G | 4.64716e-05 | 0.00482013 | missense, stop-gained, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858430 | CCAGAGGCAATGGCT[A/G]GACCCAGTGATGGTA | 405 |
rs760792350 | snp | C/G/T | 3.29643e-05 | 0.00405971 | synonymous-codon, missense | ARNT | GRCh38.p7 | 1:150817115 | AGATTTCTGAAAATC[C/G/T]TGGATCTCTATCCTG | 405 |
rs760810167 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150838191 | CAAAAACATGCTAAA[A/C]CACTTGACTTTCTTT | 405 |
rs760817645 | snp | A/C | 3.30879e-05 | 0.00406729 | missense | ARNT | GRCh38.p7 | 1:150836418 | CGGAGTCAGACACAT[A/C]CACCACCCTGCCTGT | 405 |
rs760825373 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150834423 | TACAATCCATCTGGG[G/T]ATGGAGAGTTAAATT | 405 |
rs760833917 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150875087 | ATATAAGTATTTTGC[A/G]ATGTGTGATCAGTTA | 405 |
rs760839935 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150853490 | AGTCTGCTCTAAGCC[A/G]TGTTACCAAATTTCT | 405 |
rs760875607 | snp | C/G | 1.67899e-05 | 0.00289736 | missense | ARNT | GRCh38.p7 | 1:150812055 | AACATAGTTAGATCA[C/G]GGAATTCTTCATTGT | 405 |
rs760886910 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150834782 | CTGACCAAGCAGGAG[A/T]TGAATTTTTTTTCAA | 405 |
rs760895130 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852157 | ATGACACCTCAACCA[A/G]TGAATTACACCTCTC | 405 |
rs760908636 | snp | A/G | 3.30447e-05 | 0.00406464 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836286 | AACTCTCACCTGTCA[A/G]GGCATTTTCTGAAGT | 405 |
rs761017086 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810035 | GGTTGTGGGTGCCTG[C/T]TGTTTATGAACTGGA | 405 |
rs761042840 | snp | C/T | 9.26569e-05 | 0.00680587 | intron-variant | ARNT | GRCh38.p7 | 1:150829492 | TCCACATACTGGCTA[C/T]GCTGAACTCATTACT | 405 |
rs761099353 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861420 | TTGAAAGCAGGGTCT[C/G]AAAGAAACATTTGTA | 405 |
rs761138279 | in-del | -/A/G | 4.47838e-05 | 0.0047318 | intron-variant | ARNT | GRCh38.p7 | 1:150831924 | GAGTTACAGGAGTTT[-/A/G]GAAAAAAAAAAAAAA | 405 |
rs761221616 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150854117 | AAGAGACAAGCTCTC[A/C]CTCTGTTACTCAGGC | 405 |
rs761257370 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815404 | ATACAAAAAATTAGC[C/T]AGGCGTGGTGGCGAG | 405 |
rs761276305 | snp | C/T | 1.65586e-05 | 0.00287733 | missense | ARNT | GRCh38.p7 | 1:150813315 | GTGTCTGGAATTGTC[C/T]TGCAGTCTGTCCAGT | 405 |
rs761289915 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150818562 | TTTGAGACCAGCCTG[A/G]GCAACATGGTGAAGC | 405 |
rs761326079 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150832850 | CAACTTAATGTAATT[-/G]CTACAGTTCATTATT | 405 |
rs761382580 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150842533 | AAGGAAGGGGGGAGG[C/G]AGGAAGGGAAAAAAG | 405 |
rs761405554 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150814419 | ACACTATTTTTTAGG[C/G]AGCTGAGATAAAATT | 405 |
rs761407728 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | ARNT | GRCh38.p7 | 1:150834620 | TTTTCACTGTTCCAG[C/T]CTTTAGATCCAGGAT | 405 |
rs761455085 | snp | C/T | 1.74136e-05 | 0.00295067 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817960 | TCTCCAGGGGTAAAT[C/T]AGCTGTGGGACCTAG | 405 |
rs761458854 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150869281 | AGGAGATCGAGGCCA[C/T]CCTGGCTAACACAGT | 405 |
rs761484022 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844970 | GCCCACCATGATGCC[C/T]GGCTAATTTTTATAT | 405 |
rs761486793 | snp | C/T | 3.36604e-05 | 0.00410232 | intron-variant | ARNT | GRCh38.p7 | 1:150846343 | TGTTTCAAAGCATTA[C/T]ACTTGTTATATCTAT | 405 |
rs761507962 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ARNT | GRCh38.p7 | 1:150839536 | CTGCCATGCGTAAGA[C/T]GGTTAGCTTGTCTGG | 405 |
rs761557649 | snp | A/G | 3.30109e-05 | 0.00406256 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814078 | TGGTCTGGACTCACC[A/G]AAGTTAGATCCACGA | 405 |
rs761599035 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150836526 | ATAGAAGTTAATATT[C/T]TACTCTGAAAAAACA | 405 |
rs761679283 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150824911 | CTATCGCCCAGGCTG[A/G]AGTGCAGTGGGGCAA | 405 |
rs761683931 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875266 | CTTTCCTTCAAAAAA[A/T]ATTTAAAAGATTAAA | 405 |
rs761703277 | in-del | -/AC | | | intron-variant | ARNT | GRCh38.p7 | 1:150875502 | TCTCCGCCCCACGCA[-/AC]ACACACACATATCTC | 405 |
rs761706968 | snp | C/T | 1.726e-05 | 0.00293763 | intron-variant | ARNT | GRCh38.p7 | 1:150816778 | AGCAGCACATATATA[C/T]GGGGCTCACCTGAAA | 405 |
rs761767050 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150822947 | TTTGAAATGGAGTCT[C/T]GCTCTGTAGCCCAGG | 405 |
rs761774210 | snp | C/T | 1.66305e-05 | 0.00288357 | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150852830 | AGCCAACAATAAATA[C/T]TTTAAGCCTGCTGAT | 405 |
rs761778725 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844759 | GTAATTTAAACAAAT[G/T]TAAGTTTTTTTCAAT | 405 |
rs761782155 | snp | A/C | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811411 | GGGGACAAATTTTGC[A/C]TAACTCCCTAATAGG | 405 |
rs761845087 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873415 | ATAAGTAGAACTAGT[A/G]AAAAATGATAGAATA | 405 |
rs761846810 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150853834 | GACCAATCCCCTTAT[A/G]ATCTCTGTACACTAT | 405 |
rs761850849 | in-del | -/AGAACAA | 1.67419e-05 | 0.00289321 | intron-variant | ARNT | GRCh38.p7 | 1:150814265 | ATGGAGAGGGGATAT[-/AGAACAA]ATACAGCATTAACAT | 405 |
rs761851134 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | ARNT | GRCh38.p7 | 1:150832341 | GATCTCACCTGCATC[C/T]GTTCCTCACAAAGCT | 405 |
rs761889480 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809922 | GTGAGGGGGGAGGCG[G/T]GCAATGTGATCAGAA | 405 |
rs761891026 | snp | A/G | 1.7093e-05 | 0.00292339 | intron-variant | ARNT | GRCh38.p7 | 1:150813151 | AGCTTCTAATTTTTG[A/G]AAGTCTTTTCACTCT | 405 |
rs761895179 | snp | A/G | 1.65051e-05 | 0.00287267 | intron-variant | ARNT | GRCh38.p7 | 1:150839410 | ATTCACCCAGATTCC[A/G]GACTCTCTCAGAACT | 405 |
rs761957127 | snp | C/G | 0.000132688 | 0.00814409 | utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150876569 | GTAGTCGCCGCCATG[C/G]CCGCAGATGCCACCG | 405 |
rs761972045 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150848969 | AGCACTTTGGGAGGC[A/C]GAGGTGGGCGGATCA | 405 |
rs761986223 | in-del | -/GAG | | | intron-variant | ARNT | GRCh38.p7 | 1:150863388 | TGCCAGGTAAATTCA[-/GAG]AAGATAATCCTGGTT | 405 |
rs762009206 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150841324 | CTTTGTCCAAAAAAA[A/C]AAGAAAGTAAGAAAA | 405 |
rs762023246 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868011 | TCAGGTAGTTATTTA[C/T]AGCAGTGTGAGAATG | 405 |
rs762042083 | snp | A/G | 0.000148249 | 0.00860829 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823256 | AGGGTTCTGGAAAGT[A/G]AAGGAGCTGGTTCTC | 405 |
rs762118568 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857304 | TTTATAATACTTTTG[-/T]TTGTTACTGTACATA | 405 |
rs762158765 | snp | C/G | 1.65455e-05 | 0.00287619 | missense, splice-acceptor-variant | ARNT | GRCh38.p7 | 1:150829966 | CCTCTGGGTCATCAT[C/G]TGGGAGGGAAACACC | 405 |
rs762161336 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867158 | GCGGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 405 |
rs762213698 | snp | A/T | 4.94458e-05 | 0.00497197 | missense | ARNT | GRCh38.p7 | 1:150817126 | AATCTTGGATCTCTA[A/T]CCTGGGCAAATAAAC | 405 |
rs762248309 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828936 | AGATGACAGTCCTAA[C/T]AGGAAGCTGAAAATA | 405 |
rs762286929 | snp | A/T | | | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861367 | TAGAATTACCACATG[A/T]TCCAGCAATTCCACC | 405 |
rs762295298 | in-del | -/GGG | | | intron-variant | ARNT | GRCh38.p7 | 1:150820245 | CTGCTCCAGAGGAAA[-/GGG]ATCCTGCCAGACTAG | 405 |
rs762304059 | in-del | -/TACAGA | | | intron-variant | ARNT | GRCh38.p7 | 1:150835814 | AAAAAAGAACAACAG[-/TACAGA]TACAGATACAAACAA | 405 |
rs762336572 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | ARNT | GRCh38.p7 | 1:150817320 | GAACACTTCCTAAGT[A/G]AATACTCCCTACCCT | 405 |
rs762339056 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150823590 | GAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC | 405 |
rs762347469 | snp | G/T | 2.38172e-05 | 0.0034508 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858438 | AATGGCTGGACCCAG[G/T]GATGGTACATCTGAT | 405 |
rs762355489 | snp | A/G | 2.26091e-05 | 0.00336215 | intron-variant | ARNT | GRCh38.p7 | 1:150818061 | AGACAGTAAAGAGGG[A/G]GTGGAGAGGGAGGAA | 405 |
rs762357194 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861655 | TCTCTAAAAAAAATG[A/G]ACAAAATTGGCCATA | 405 |
rs762407426 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150864486 | ACGAAATTGGAAATC[A/G]TCATTCTCAGTAAAC | 405 |
rs762446224 | in-del | -/AA | 0.00446925 | 0.0470601 | intron-variant | ARNT | GRCh38.p7 | 1:150853282 | GCAAGACTCCATCTC[-/AA]AAAAAAAAAGTACAA | 405 |
rs762537834 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | ARNT | GRCh38.p7 | 1:150814086 | ACTCACCAAAGTTAG[A/G]TCCACGATTGGTGAG | 405 |
rs762542824 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150862342 | CTGCCAAGGAGGTTA[C/T]ACCAATTTAAAGCCT | 405 |
rs762544813 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840801 | ATATCACTGTTAACA[C/G]GAATAATCCAGCAGT | 405 |
rs762582128 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150861450 | TACCCACGTTCACAG[-/A]AAGTACTATTCAACA | 405 |
rs762600895 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150861200 | TAGAAAACAGTATGG[A/C]GATGCCTCCAAAAAT | 405 |
rs762604963 | snp | G/T | 3.58269e-05 | 0.00423228 | intron-variant | ARNT | GRCh38.p7 | 1:150829514 | CTCATTACTCAGGTT[G/T]ATATGGTACAAGTAA | 405 |
rs762611389 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811316 | AATATTCTTTGGCTG[C/T]AATACTAAGTGGAAA | 405 |
rs762614187 | in-del | -/T | 0.00587572 | 0.0538826 | intron-variant | ARNT | GRCh38.p7 | 1:150826650 | GAGTAAGATATATAC[-/T]TTTTTTTTTTTAAGA | 405 |
rs762622516 | snp | A/T | 1.6473e-05 | 0.00286988 | missense | ARNT | GRCh38.p7 | 1:150832358 | TTCCTCACAAAGCTC[A/T]GCCTATTCACAGAAA | 405 |
rs762681493 | snp | A/T | 1.68564e-05 | 0.00290309 | intron-variant | ARNT | GRCh38.p7 | 1:150842512 | AAATTAAAATAAAAA[A/T]GAAGGAAGGAAGGGG | 405 |
rs762735523 | snp | A/G | | | missense | ARNT | GRCh38.p7 | 1:150817118 | TTTCTGAAAATCTTG[A/G]ATCTCTATCCTGGGC | 405 |
rs762805072 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853629 | ACTTCATTCAAGACA[C/T]TGTGCTAGGTGAGGT | 405 |
rs762809013 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150830382 | GCAAAACAAAACAAA[A/G]TACATCTAGTTATGA | 405 |
rs762820883 | snp | A/G | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811229 | ATCGTATCAACAGCC[A/G]ACTTTCTATATTTGC | 405 |
rs762891302 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870843 | CATAAACTTACTTGT[C/T]CATTCAACTACAATG | 405 |
rs762900585 | snp | G/T | 1.64838e-05 | 0.00287083 | intron-variant | ARNT | GRCh38.p7 | 1:150834647 | GGATACGCCCTGAAG[G/T]AAGATGTGAAGAGCA | 405 |
rs762949862 | snp | C/T | 1.72421e-05 | 0.00293611 | synonymous-codon, intron-variant | ARNT | GRCh38.p7 | 1:150817973 | ATTAGCTGTGGGACC[C/T]AGTTGTGGCCTCTGG | 405 |
rs762987410 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150822454 | GCCAATGATTTAATC[A/G]CTCATGGCTACATAA | 405 |
rs763000280 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150814624 | AGGCAGGCAGACCAC[C/G]TGAGGTGAGGAGTTC | 405 |
rs763047576 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821828 | AATTTTTGTATTTTC[-/T]TTTTTTTTTTTTTTT | 405 |
rs763048863 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150822008 | AGCATTTTTACTTTT[C/T]ATAATAGATTTGTAT | 405 |
rs763077740 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849143 | GGGAGGCAGAGGTTG[C/T]GGTGAGCCGAGATCA | 405 |
rs763085947 | snp | C/T | | | missense | ARNT | GRCh38.p7 | 1:150814188 | GAGTCTGAAAGCTGC[C/T]CACACCAAACTGGGA | 405 |
rs763088080 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810702 | GGTGAGGGTAGTAAC[C/T]TGTATCCGCATTTAT | 405 |
rs763091380 | snp | A/C | 1.70793e-05 | 0.00292222 | intron-variant | ARNT | GRCh38.p7 | 1:150816785 | CATATATACGGGGCT[A/C]ACCTGAAATTCTCTG | 405 |
rs763112809 | in-del | -/AAAAAAAAAA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809639 | CACACACACACAAAA[-/AAAAAAAAAA]AAAAAAAAGTTGCTA | 405 |
rs763121654 | snp | C/T | 0.000214142 | 0.0103453 | missense | ARNT | GRCh38.p7 | 1:150839499 | GTGTTGCCAGTTCCC[C/T]GCAAGGACTTCATGT | 405 |
rs763137274 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863046 | ACAGAGCAAGATTCC[A/G]TCTCAAAAAAAAAAA | 405 |
rs763208829 | in-del | -/TAAC | 1.69327e-05 | 0.00290965 | intron-variant | ARNT | GRCh38.p7 | 1:150814281 | GAACAAATACAGCAT[-/TAAC]ATCATTGCACATACC | 405 |
rs763216096 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877563 | TTGGAGGCAATAGAT[A/G]AAGAAAGTAATTTGA | 405 |
rs763218899 | snp | C/T | 1.70203e-05 | 0.00291716 | intron-variant | ARNT | GRCh38.p7 | 1:150826660 | TATACTTTTTTTTTT[C/T]TAAGATGGAGTTTCG | 405 |
rs763222414 | snp | A/G | 1.72374e-05 | 0.00293571 | intron-variant | ARNT | GRCh38.p7 | 1:150852852 | CCTGCTGATAATACA[A/G]AACATTAAGAAGTTA | 405 |
rs763305606 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | ARNT | GRCh38.p7 | 1:150817333 | GTAAATACTCCCTAC[C/T]CTCTTCAACGAAGAG | 405 |
rs763331192 | snp | A/C | 0.000224997 | 0.0106041 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876589 | AGATGCCACCGCCGC[A/C]GCGCCACCCCCCCCC | 405 |
rs763360757 | snp | C/T | 1.65518e-05 | 0.00287674 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813205 | GCCAGGTTGCTGTGC[C/T]GGCGGTTGTTGAACA | 405 |
rs763397458 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150815229 | GTGTATTTATTGTGC[A/G]TTATATTATATATAT | 405 |
rs763422140 | in-del | -/TTCT | | | intron-variant | ARNT | GRCh38.p7 | 1:150835230 | ATAGATCTGTTTGTC[-/TTCT]TTATTATACAGAAAC | 405 |
rs763469689 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824697 | TGACCTCAAATGATC[C/T]GCCTGCCTTGGCCTC | 405 |
rs763479338 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150867546 | AAAAGAGAGAGATAT[A/C]TTTTAAATAGATAAA | 405 |
rs763487700 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150831532 | TAAGTTTCTTTGCAA[C/T]AAATGCTTAGAATAC | 405 |
rs763546364 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150826227 | GACGAGGAAAACATC[C/T]ATTTTCACAGCATCT | 405 |
rs763569351 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | ARNT | GRCh38.p7 | 1:150839424 | CAGACTCTCTCAGAA[C/T]TATAAGTCCCAGAGA | 405 |
rs763577588 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150829757 | AAGAATAGCAATGGT[C/T]ACTATAAATGCCATA | 405 |
rs763598275 | snp | A/G | 1.65674e-05 | 0.00287809 | intron-variant | ARNT | GRCh38.p7 | 1:150817459 | AAGGCCAGTTGACAA[A/G]ACAAATAGAAAAAAA | 405 |
rs763694765 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | ARNT | GRCh38.p7 | 1:150817357 | CGAAGAGGACACAAC[C/T]CACCTGGGAATGATT | 405 |
rs763699854 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150867288 | TAATCCCAGCTACTA[C/G]GGAGACCAAGATGGG | 405 |
rs763705266 | snp | A/C | 4.10366e-05 | 0.00452953 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876601 | CGCCGCGCCACCCCC[A/C]CCCCCAGTGGGAGGA | 405 |
rs763722704 | snp | C/T | 3.30764e-05 | 0.00406659 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813310 | TGTCCGTGTCTGGAA[C/T]TGTCCTGCAGTCTGT | 405 |
rs763732376 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ARNT | GRCh38.p7 | 1:150832335 | ACTTAGGATCTCACC[C/T]GCATCTGTTCCTCAC | 405 |
rs763737942 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838988 | TTCATAGTGATCACA[C/T]GTAACAGAGCACATC | 405 |
rs763745736 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813229 | TTGAACATGTTGCTC[A/G]CTAGAACTTGAACGA | 405 |
rs763777822 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835310 | TAAAAACATAAAGGA[A/G]GGGAAAACTGGTCAA | 405 |
rs763992759 | snp | A/G | 3.57935e-05 | 0.00423031 | intron-variant | ARNT | GRCh38.p7 | 1:150846229 | AACATGGATCATATT[A/G]TATATTACAATATAT | 405 |
rs763997959 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150834888 | AGGAAAAGTAGGAGT[A/G]GAAAGTAGTAGTAGA | 405 |
rs764014521 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150845911 | TGTCTCAAAATAAAT[A/G]AATTAATTACAGAAC | 405 |
rs764019554 | in-del | -/A | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878428 | CTACAAAGTACTTCC[-/A]ATTTTCATGTATCGC | 405 |
rs764027746 | snp | C/G | 2.32426e-05 | 0.00340892 | missense, synonymous-codon, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858431 | CAGAGGCAATGGCTG[C/G]ACCCAGTGATGGTAC | 405 |
rs764063569 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150852299 | TTGCACACTGGGATT[G/T]GTGCTGTAGATTGTA | 405 |
rs764081227 | snp | A/T | 1.6513e-05 | 0.00287336 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836305 | ATTTTCTGAAGTGGA[A/T]AGCTGCTCACGAAGT | 405 |
rs764092906 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870986 | AGCCGGGGCAATATA[G/T]TGAGACCCGGTCACT | 405 |
rs764098363 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810142 | TCTTTGCTACATGTC[A/T]TTATTTTTGCCACTG | 405 |
rs764112461 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824924 | TGGAGTGCAGTGGGG[C/T]AATCTTGGGTCACTG | 405 |
rs764121117 | snp | A/G | 1.68029e-05 | 0.00289848 | intron-variant | ARNT | GRCh38.p7 | 1:150846339 | GGATTGTTTCAAAGC[A/G]TTACACTTGTTATAT | 405 |
rs764125240 | snp | C/T | 1.75422e-05 | 0.00296155 | intron-variant | ARNT | GRCh38.p7 | 1:150830029 | GACCTCCAACTCAAA[C/T]GCCTTCAAAACTCAG | 405 |
rs764178755 | snp | A/G | 1.65119e-05 | 0.00287327 | missense | ARNT | GRCh38.p7 | 1:150831890 | CCCCATCCTTTACAG[A/G]GCCAAGTCCATTCCT | 405 |
rs764244725 | in-del | -/A | 0.00990075 | 0.0696588 | intron-variant | ARNT | GRCh38.p7 | 1:150853282 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAGTACA | 405 |
rs764268164 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150867070 | AAATTAGCCAGGCGT[C/G]GTGGCACACTGTAGT | 405 |
rs764292322 | snp | G/T | 5.91681e-05 | 0.0054388 | intron-variant | ARNT | GRCh38.p7 | 1:150818080 | GAGAGGGAGGAAGGG[G/T]GGAGAGAGAGAGAAA | 405 |
rs764309415 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865251 | CTTCACTCACACACA[A/G]GAAAAAAATTTTTAA | 405 |
rs764343466 | snp | A/C/G | 6.7056e-05 | 0.00579 | intron-variant | ARNT | GRCh38.p7 | 1:150814263 | AGATGGAGAGGGGAT[A/C/G]TAGAACAAATACAGC | 405 |
rs764343636 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | ARNT | GRCh38.p7 | 1:150823221 | TTGGTACAGATGATG[C/T]ACTCAATTTCATCTG | 405 |
rs764360746 | snp | C/G | 1.65471e-05 | 0.00287633 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836419 | GGAGTCAGACACATA[C/G]ACCACCCTGCCTGTC | 405 |
rs764396740 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844496 | ATATTTCTAATCTCT[C/T]TACATCAACGGTTCT | 405 |
rs764444052 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150830652 | ATTTATGCTTTGCCT[A/C]ATCTGTAACTTTTAA | 405 |
rs764450027 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150849060 | AATACAAAATTAGCC[A/G]GGCATGGTAGTGCAT | 405 |
rs764470107 | snp | C/T | 1.77811e-05 | 0.00298165 | intron-variant | ARNT | GRCh38.p7 | 1:150829499 | ACTGGCTATGCTGAA[C/T]TCATTACTCAGGTTG | 405 |
rs764534801 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877696 | GGCGCAATCTCGGCT[C/T]ACTGCAACCTCCACC | 405 |
rs764602038 | snp | A/G | 4.95282e-05 | 0.00497611 | intron-variant | ARNT | GRCh38.p7 | 1:150817035 | GGCATGCCCATCAGT[A/G]AGTGATCTAAATGAG | 405 |
rs764604068 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150853780 | AGAAGAAGTGAATTT[A/C]TTTAAAGGAGATTAG | 405 |
rs764620093 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815390 | CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCCA | 405 |
rs764626976 | snp | C/T | 2.84929e-05 | 0.00377434 | missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858355 | CAAACTCACCCTGGT[C/T]GCCGCTTAATAGCCC | 405 |
rs764682536 | snp | A/C | 0.000383362 | 0.0138396 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876606 | CGCCACCCCCCCCCC[A/C]AGTGGGAGGAGCCGC | 405 |
rs764700305 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150839296 | TCATTGTCCCAATGC[C/T]AATTAATGTTATAGC | 405 |
rs764712207 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150813549 | TAGAGTTCTTTACTC[A/G]TTTAGGTTAAATGTG | 405 |
rs764740001 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840688 | GAGGAGTGGAATGGA[A/G]AGGAGGATGATTAAA | 405 |
rs764801107 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150837747 | AGACATGACTAACGT[C/T]TTTTCCTGAGCTTTC | 405 |
rs764821600 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810998 | GGCTAATCCAAGAAG[C/T]TGAGTTTCCATGCAG | 405 |
rs764839866 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150843504 | GGTCAATAGGCAGAA[A/T]ATAACACAGTAACAA | 405 |
rs764842202 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858119 | AGTCCTTTATCTTAC[A/G]GAAATTTTGGTTTAA | 405 |
rs764851308 | snp | C/T | 1.65326e-05 | 0.00287507 | missense | ARNT | GRCh38.p7 | 1:150829106 | ACCTGTGGCTGGTAG[C/T]CAACAGTAGCCACAC | 405 |
rs764859178 | snp | C/T | 1.7312e-05 | 0.00294205 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817966 | GGGGTAAATTAGCTG[C/T]GGGACCTAGTTGTGG | 405 |
rs764861223 | snp | A/G | 1.66751e-05 | 0.00288744 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813328 | TCCTGCAGTCTGTCC[A/G]GTCTCAGGAGCTAGA | 405 |
rs764902900 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150852230 | GGAACATATGACTTG[C/T]TTTGGCCAATGGGAC | 405 |
rs764916358 | snp | A/G | 6.60099e-05 | 0.00574461 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814081 | TCTGGACTCACCAAA[A/G]TTAGATCCACGATTG | 405 |
rs764918927 | in-del | -/AGTC | | | intron-variant | ARNT | GRCh38.p7 | 1:150866279 | TGAGCCACCAAGGTC[-/AGTC]AGCCTGTTCCAAGGT | 405 |
rs764922089 | snp | C/T | 3.32347e-05 | 0.00407631 | intron-variant | ARNT | GRCh38.p7 | 1:150842389 | AAAAAGCAGCATCAT[C/T]TGCTTCATCATGCTA | 405 |
rs764940535 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150832698 | CCAGAAAGTCTGTTG[C/T]AACTAGTCAACTCTA | 405 |
rs764949832 | snp | C/T | 1.69231e-05 | 0.00290882 | intron-variant | ARNT | GRCh38.p7 | 1:150852845 | CTTTAAGCCTGCTGA[C/T]AATACAAAACATTAA | 405 |
rs764957510 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150834047 | TCAAGCAATTGTCCT[A/G]CCTCAGCCTCCAAGT | 405 |
rs764976996 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150873491 | TTCAACACAACTCTT[-/A]AGAGAGTACCAACCA | 405 |
rs764984732 | in-del | -/TTTAA | | | intron-variant | ARNT | GRCh38.p7 | 1:150838346 | AGAACTAGTTCTATG[-/TTTAA]TTTATTTATTTACAT | 405 |
rs764994544 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150826111 | GTAGACATGGGGTTT[C/G]ACTGTGTTGGCCAGG | 405 |
rs765000233 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846163 | TAAACAGAGAAATTC[C/T]GTCTCATCCAGAAAA | 405 |
rs765081387 | snp | A/G | 2.12863e-05 | 0.00326232 | intron-variant | ARNT | GRCh38.p7 | 1:150831921 | AGAAGAGTTACAGGA[A/G]TTTGAAAAAAAAAAA | 405 |
rs765097980 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150849152 | AGGTTGCGGTGAGCC[A/G]AGATCATACCATTGC | 405 |
rs765162453 | in-del | -/AAT | | | intron-variant | ARNT | GRCh38.p7 | 1:150843518 | AAATAACACAGTAAC[-/AAT]GAAGAAGAATGTAAA | 405 |
rs765202593 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150831749 | GGTATATAATAAATA[C/T]TAGCTTTCATGGACT | 405 |
rs765218514 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868186 | CAAGCCGGGCACTGT[A/G]GTGTACACTTGTAAT | 405 |
rs765281853 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863906 | TGAAAATACAGTTAT[A/G]TATCACTTAACAACA | 405 |
rs765300913 | snp | A/G/T | 7.07583e-05 | 0.00594769 | intron-variant | ARNT | GRCh38.p7 | 1:150817478 | AATAGAAAAAAAAAT[A/G/T]TTTTTTAAAAAAGAA | 405 |
rs765314219 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ARNT | GRCh38.p7 | 1:150816282 | AAAAGCCTGAGCGGG[C/T]AGTAGGGGTCCAAGT | 405 |
rs765334960 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150856908 | GGCTGCAGTGGGCCA[C/T]GATTGTGCCTCTGCA | 405 |
rs765368875 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820313 | AAAGAGTTGATACAT[A/T]GAATTGAAACTAAAC | 405 |
rs765373632 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865654 | AGAGTATAAATCAAA[G/T]GTCTTACAGTCTAGT | 405 |
rs765377379 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150863587 | TAATCCCAACACTTT[G/T]GGAGGCCGAGGTGGG | 405 |
rs765435129 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150819503 | TGATAACCAAGAAGT[A/C]GAAACAACCAAATGT | 405 |
rs765440766 | snp | A/T | 0.00163722 | 0.0285644 | intron-variant | ARNT | GRCh38.p7 | 1:150826500 | TATTTATGGAGTGAA[A/T]ATGACAAATATTTAT | 405 |
rs765441563 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854462 | TTGGGTTGGGGGGGC[A/G]GGAGGGGCTGCAGGC | 405 |
rs765502857 | in-del | -/TAA | 3.66898e-05 | 0.00428294 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858480 | AGGAAAATAATGAAG[-/TAA]TAAACATTTTTAAAA | 405 |
rs765526565 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863762 | GCAGAGGTTGCAGTG[A/G]GCCAATCGAGCCACT | 405 |
rs765536709 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150875666 | ACATAGAGGAAAGAG[A/G]GCTGGGACTAGTAAT | 405 |
rs765541010 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150855966 | AAAATGTGTGTGTGC[C/G]TGTGTATTGCTTATT | 405 |
rs765560362 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811938 | AAGGGAGAGGAACTT[C/T]TATTCTGTTTACAGA | 405 |
rs765561969 | snp | A/T | 1.66721e-05 | 0.00288717 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150816404 | GGGGCTAGGCCACTA[A/T]TCCTAGGAGTGAATA | 405 |
rs765586486 | snp | A/G | 0.000230875 | 0.0107417 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813286 | TGGCCAGACACCCAC[A/G]CCCTCTGCTGTCCGT | 405 |
rs765612297 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817131 | TGGATCTCTATCCTG[A/G]GCAAATAAACCATCT | 405 |
rs765634134 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150839340 | TCGTTTTCCCATTGT[C/G]TGACTTCTTCCTGAA | 405 |
rs765705399 | snp | A/G | 3.3502e-05 | 0.00409266 | synonymous-codon | ARNT | GRCh38.p7 | 1:150812072 | GAATTCTTCATTGTT[A/G]TAGCTGTTGCTCTGA | 405 |
rs765713018 | snp | C/T | 9.64065e-05 | 0.00694218 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858441 | GGCTGGACCCAGTGA[C/T]GGTACATCTGATGTC | 405 |
rs765720006 | snp | A/G | 1.66175e-05 | 0.00288244 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813184 | TACCTGGAAGACCTC[A/G]GGCTGGCCAGGTTGC | 405 |
rs765721574 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824070 | ATGGTCTCGATTTCC[C/T]GACCTCGGGATCCGC | 405 |
rs765737447 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150829600 | TTAGTCAGGTAATGA[C/T]ACAATGAAAAGGATC | 405 |
rs765817504 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846834 | TCTATGAATTTGACT[A/T]CTTGTAGATACCTCA | 405 |
rs765825296 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827662 | TCTATGGGTGAACAT[G/T]TTTTCATTTCTCTTA | 405 |
rs765839596 | snp | C/T | 9.90671e-05 | 0.00703731 | missense | ARNT | GRCh38.p7 | 1:150836324 | TGCTCACGAAGTTTA[C/T]CCACATCATCTGGGT | 405 |
rs765867480 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150812950 | TGATCCCCTGCTTCA[C/G]CCTTCTAAGGGGCTG | 405 |
rs765876914 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857941 | CTCTGCATTCCAAAC[C/G]AAGCAACATATCAAT | 405 |
rs765896791 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836434 | CACCACCCTGCCTGT[C/T]TCACATGAGACAATA | 405 |
rs765906531 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150821775 | TACCTTAACCTCCCA[A/C]GTAGCTGGGACTATA | 405 |
rs765936452 | snp | A/C | 1.69795e-05 | 0.00291367 | intron-variant | ARNT | GRCh38.p7 | 1:150842519 | AATAAAAAAGAAGGA[A/C]GGAAGGGGGGAGGGA | 405 |
rs765999490 | snp | A/G | 1.79416e-05 | 0.00299507 | intron-variant | ARNT | GRCh38.p7 | 1:150829515 | TCATTACTCAGGTTG[A/G]TATGGTACAAGTAAC | 405 |
rs766011274 | snp | A/G | 1.64814e-05 | 0.00287061 | missense | ARNT | GRCh38.p7 | 1:150814209 | CAAACTGGGAAGTAC[A/G]AGTCTTAGCAGTAGC | 405 |
rs766021304 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854213 | ATCTTGGCCTCCCAA[A/T]TAGCTGGAACTATAG | 405 |
rs766058627 | snp | C/T | 0.000148939 | 0.00862828 | synonymous-codon, splice-acceptor-variant | ARNT | GRCh38.p7 | 1:150829967 | CTCTGGGTCATCATC[C/T]GGGAGGGAAACACCT | 405 |
rs766058796 | snp | A/G | 1.65034e-05 | 0.00287253 | intron-variant | ARNT | GRCh38.p7 | 1:150817056 | TCTAAATGAGAATTT[A/G]AAAGGATAATGAGAA | 405 |
rs766069339 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820022 | TGAAAGAGGAGGATG[A/T]AGCTATGCTCTAAAG | 405 |
rs766119017 | snp | A/G | 1.64838e-05 | 0.00287083 | intron-variant | ARNT | GRCh38.p7 | 1:150834649 | ATACGCCCTGAAGGA[A/G]GATGTGAAGAGCAGT | 405 |
rs766138114 | in-del | -/ATATTGGGAT | | | intron-variant | ARNT | GRCh38.p7 | 1:150832906 | ATTAGCCATGTCCAC[-/ATATTGGGAT]ACTCCTGCCAATGCT | 405 |
rs766157326 | in-del | -/G | 3.299e-05 | 0.00406127 | intron-variant | ARNT | GRCh38.p7 | 1:150816910 | GGACCAAAAGGAGTT[-/G]GGGAAGGGCCAGTCA | 405 |
rs766159773 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838720 | ATGATCATGTTATTT[C/T]AATAACCAAAACAGA | 405 |
rs766170284 | snp | G/T | 8.6227e-05 | 0.00656552 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817978 | CTGTGGGACCTAGTT[G/T]TGGCCTCTGGATTGT | 405 |
rs766337164 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150870793 | GGATTACAGGTATGA[A/G]CCACCATGTCCAGCC | 405 |
rs766396389 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150818619 | TAGCAGGCGTGGTGG[C/T]GGGCTCCTGTAGTCC | 405 |
rs766401531 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150839119 | TTCTTCCATCTTCTA[C/T]AACCCTAAAGGCAAG | 405 |
rs766490173 | snp | A/T | 1.64906e-05 | 0.00287142 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814087 | CTCACCAAAGTTAGA[A/T]CCACGATTGGTGAGA | 405 |
rs766523151 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150863189 | CAACACGGCAAAATC[C/T]CGTCTCTACTAAAAA | 405 |
rs766546722 | in-del | -/C | 1.70901e-05 | 0.00292314 | intron-variant | ARNT | GRCh38.p7 | 1:150814287 | ATACAGCATTAACAT[-/C]ATTGCACATACCATG | 405 |
rs766561322 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859793 | GGTGGGCAGATCACT[C/T]GAGCCCAGGAGTTCG | 405 |
rs766567249 | snp | C/T | 1.68193e-05 | 0.00289989 | synonymous-codon | ARNT | GRCh38.p7 | 1:150816799 | TCACCTGAAATTCTC[C/T]GCCGGCCGGGGGGTA | 405 |
rs766570804 | snp | C/G | | | missense | ARNT | GRCh38.p7 | 1:150834611 | GACCTTCCTTTTTCA[C/G]TGTTCCAGTCTTTAG | 405 |
rs766584946 | snp | A/C | 1.7235e-05 | 0.00293551 | intron-variant | ARNT | GRCh38.p7 | 1:150852853 | CTGCTGATAATACAA[A/C]ACATTAAGAAGTTAA | 405 |
rs766598492 | snp | A/G | 1.70965e-05 | 0.00292369 | intron-variant | ARNT | GRCh38.p7 | 1:150826663 | ACTTTTTTTTTTTTA[A/G]GATGGAGTTTCGCTC | 405 |
rs766603952 | snp | A/T | 0.000454545 | 0.0150687 | intron-variant | ARNT | GRCh38.p7 | 1:150861337 | AACATCGCAAAAAAA[A/T]AATTAAATTAAAAAT | 405 |
rs766634271 | in-del | -/ATTTTC | | | intron-variant | ARNT | GRCh38.p7 | 1:150821823 | CCAGCTAATTTTTGT[-/ATTTTC]TTTTTTTTTTTTTTT | 405 |
rs766639816 | snp | G/T | 4.17563e-05 | 0.00456907 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858322 | TTTATAGGAGAGATA[G/T]TCATAACACACTACA | 405 |
rs766647758 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815857 | GACAGAGCAAGACTC[-/T]TGTCTCAAAAAAAAA | 405 |
rs766697932 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861929 | CCACTGCAGGCTAAT[G/T]TAAGTATTCCACACA | 405 |
rs766699732 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150826450 | GAACATAAAACTGTA[A/G]TGCCTGCCACAGTGT | 405 |
rs766756351 | snp | A/G | 4.9666e-05 | 0.00498302 | missense | ARNT | GRCh38.p7 | 1:150813209 | GGTTGCTGTGCTGGC[A/G]GTTGTTGAACATGTT | 405 |
rs766769475 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150843226 | ATTCCCTCTCCACTG[G/T]AGAAGGATACAAAGA | 405 |
rs766771969 | snp | C/G | 0.015747 | 0.0873244 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876597 | CCGCCGCCGCGCCAC[C/G]CCCCCCCCCAGTGGG | 405 |
rs766775019 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824291 | CCAGGAAGGAAAAGA[C/T]TGTTTCCCTACTTCC | 405 |
rs766851927 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150815498 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 405 |
rs766867823 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857908 | GGAATTTAATAAATA[-/C]TTTTGGAGCTGAATG | 405 |
rs766888531 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857971 | TAACTTAGAAGACAG[C/G]TATTCTAGAGCTCAG | 405 |
rs766899578 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150826463 | TAGTGCCTGCCACAG[C/T]GTTCAGTTAATCAGT | 405 |
rs766912362 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845605 | GGAGTGAGACTCTGT[C/T]TCAAAAAAATAAAAT | 405 |
rs766948241 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871222 | TAAAATGATAGGTGT[C/T]GTCATATTTCCAACC | 405 |
rs766963686 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150865538 | GAATTAGTTCAGCAT[A/C]TGTTTACTACAGAGA | 405 |
rs766979876 | snp | A/T | 1.6486e-05 | 0.00287102 | intron-variant | ARNT | GRCh38.p7 | 1:150839425 | AGACTCTCTCAGAAC[A/T]ATAAGTCCCAGAGAC | 405 |
rs767032946 | snp | C/G | 1.65356e-05 | 0.00287533 | missense | ARNT | GRCh38.p7 | 1:150826555 | TACCTGTTGGAAGCT[C/G]TCTCTTAGAAGCTGC | 405 |
rs767085651 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827333 | TCTGCAGTCAATCTC[C/T]GCTCCCACTCCAACT | 405 |
rs767096765 | in-del | -/AA | | | intron-variant | ARNT | GRCh38.p7 | 1:150833733 | CAGTATATAATTTAT[-/AA]ACACTAAACACCTAC | 405 |
rs767144943 | snp | A/G | 1.64866e-05 | 0.00287106 | missense | ARNT | GRCh38.p7 | 1:150817174 | GGCTTGCTGTGTTCT[A/G]GTCCTGTGGTTGTCA | 405 |
rs767168913 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820557 | AGCTACTCAGGGGAC[G/T]GAGGTGGGAGGATCA | 405 |
rs767192921 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150869423 | CGGAGCTTGCAGTGA[A/G]CTGAGATCGTGCCAC | 405 |
rs767200065 | snp | C/T | 1.6941e-05 | 0.00291036 | synonymous-codon | ARNT | GRCh38.p7 | 1:150812102 | ATCTCCCAGCATGGA[C/T]AGCATCTCCTGATAA | 405 |
rs767299915 | snp | A/G | 1.66142e-05 | 0.00288216 | intron-variant | ARNT | GRCh38.p7 | 1:150814250 | ACCTGCTAAAGAGAG[A/G]TGGAGAGGGGATATA | 405 |
rs767352759 | snp | C/T | 1.66333e-05 | 0.00288381 | intron-variant, missense | ARNT | GRCh38.p7 | 1:150842439 | CTGGCAAGTCTCTCT[C/T]TATCCGCAGAGCTCT | 405 |
rs767386898 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819153 | GAGGTGGATTCAAGG[C/T]CAATTCTACAGAAAG | 405 |
rs767396774 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150834374 | TGGCAAGTTCAGAAA[C/T]GTTAGTTCCCTTTCC | 405 |
rs767451020 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150834185 | ACCTCAGGTGATCCA[C/T]TCGCCTCAGCCTCCT | 405 |
rs767462331 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150837876 | AAAAAAAAAACCTGC[C/T]GTGCTCTTCCAATAT | 405 |
rs767506147 | snp | C/T | 0.000156894 | 0.00885563 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858329 | GAGAGATATTCATAA[C/T]ACACTACACTCAAAC | 405 |
rs767513674 | in-del | -/TATC | | | intron-variant | ARNT | GRCh38.p7 | 1:150865209 | ATAGTGAATTAAATG[-/TATC]TATCTATTTCTACTC | 405 |
rs767533141 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150817039 | TGCCCATCAGTAAGT[G/T]ATCTAAATGAGAATT | 405 |
rs767542779 | snp | A/T | 1.6836e-05 | 0.00290133 | intron-variant | ARNT | GRCh38.p7 | 1:150816416 | CTATTCCTAGGAGTG[A/T]ATAAATGAGGTAAAA | 405 |
rs767580210 | in-del | -/CA | 9.41132e-05 | 0.00685914 | intron-variant | ARNT | GRCh38.p7 | 1:150829500 | TGGCTATGCTGAACT[-/CA]CATTACTCAGGTTGA | 405 |
rs767585567 | snp | A/T | 1.75733e-05 | 0.00296418 | intron-variant | ARNT | GRCh38.p7 | 1:150852863 | TACAAAACATTAAGA[A/T]GTTAAAATTTCTCAA | 405 |
rs767587574 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816141 | ATGGAAATTGGAAAC[C/T]GGAGAACAGGGGTTG | 405 |
rs767701306 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875716 | AGAACTGCACTACAC[C/T]CTACTCCATCTCTTA | 405 |
rs767724727 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | ARNT | GRCh38.p7 | 1:150839438 | ACTATAAGTCCCAGA[A/G]ACCTGATCAGTGAGG | 405 |
rs767732051 | snp | A/G | 3.29973e-05 | 0.00406172 | intron-variant | ARNT | GRCh38.p7 | 1:150816912 | ACCAAAAGGAGTTGG[A/G]GAAGGGCCAGTCAAG | 405 |
rs767774379 | snp | C/T | 1.65302e-05 | 0.00287486 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836281 | CACATAACTCTCACC[C/T]GTCAGGGCATTTTCT | 405 |
rs767780021 | snp | C/T | 1.65425e-05 | 0.00287593 | synonymous-codon | ARNT | GRCh38.p7 | 1:150826570 | GTCTCTTAGAAGCTG[C/T]TGGTCTTCAGGATGA | 405 |
rs767784545 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825469 | GCCATGTCTATAAAA[A/T]TCACCAGATATTTTC | 405 |
rs767793481 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150817457 | CAAAGGCCAGTTGAC[A/G]AGACAAATAGAAAAA | 405 |
rs767814140 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150862694 | TAGCCTGAGCAACAT[A/G]GTGAGATCCTGCCTC | 405 |
rs767848442 | snp | G/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811640 | TCTCCTCCACTCTCT[G/T]CAGAATTTCTTTCCA | 405 |
rs767902953 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853933 | TACCTTGATATTATG[G/T]GCCTCTAGATGGGTC | 405 |
rs767917511 | snp | C/T | 0.000230635 | 0.0107361 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817430 | TGTTTGCTGTTGCTG[C/T]TGCCTATATGTCAAA | 405 |
rs768051482 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150821823 | CCAGCTAATTTTTGT[-/A]TTTTCTTTTTTTTTT | 405 |
rs768058132 | snp | C/G | 1.65507e-05 | 0.00287664 | missense | ARNT | GRCh38.p7 | 1:150829099 | GCTCCTCACCTGTGG[C/G]TGGTAGCCAACAGTA | 405 |
rs768095727 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844745 | CATCATCTTGATAGG[C/T]AATTTAAACAAATTT | 405 |
rs768124505 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150855732 | CGTAGTGAGACCATG[G/T]CTTTAAAAAAAAAAA | 405 |
rs768169163 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150862410 | CTGTGTTTTGGGAAT[A/C]CTTCAAATTTGTGGT | 405 |
rs768182420 | snp | C/G/T | 3.33914e-05 | 0.00408592 | missense | ARNT | GRCh38.p7 | 1:150816806 | AAATTCTCTGCCGGC[C/G/T]GGGGGGTAGGAGGGA | 405 |
rs768218887 | in-del | -/CCC | 3.27949e-05 | 0.00404925 | intron-variant | ARNT | GRCh38.p7 | 1:150817874 | GATTGCAAATGACCA[-/CCC]CCTGGGTGACTGCTC | 405 |
rs768220766 | snp | A/C/G | 5.03368e-05 | 0.00501656 | intron-variant | ARNT | GRCh38.p7 | 1:150842493 | GAATTAATGAACTAA[A/C/G]CTAAAATTAAAATAA | 405 |
rs768306839 | in-del | -/GTAGCCACCTGC | 0.000132063 | 0.00812491 | intron-variant, splice-acceptor-variant | ARNT | GRCh38.p7 | 1:150814229 | TTAGCAGTAGCCTGG[-/GTAGCCACCTGC]TAAAGAGAGATGGAG | 405 |
rs768316974 | snp | C/G | 0.000877578 | 0.0209289 | intron-variant | ARNT | GRCh38.p7 | 1:150853267 | GCCTGGGCGACAACT[C/G]CAAGACTCCATCTCA | 405 |
rs768370212 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | ARNT | GRCh38.p7 | 1:150834609 | CTGACCTTCCTTTTT[C/T]ACTGTTCCAGTCTTT | 405 |
rs768489957 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150822867 | GATAGTGAACTGAAT[G/T]GAATGGAAGGACACC | 405 |
rs768493007 | snp | C/G | 1.65135e-05 | 0.00287341 | intron-variant | ARNT | GRCh38.p7 | 1:150834687 | GCATTTTTGTGTGTG[C/G]GGAAGAGGGGGAGAG | 405 |
rs768511265 | snp | A/G | 4.95814e-05 | 0.00497878 | missense | ARNT | GRCh38.p7 | 1:150816380 | GATGGCTGGACAATG[A/G]TTACAGGAGGGGCTA | 405 |
rs768549568 | in-del | -/GT | | | intron-variant | ARNT | GRCh38.p7 | 1:150873779 | AAAAAATGTATCCAG[-/GT]GTGGTGGTGTGTGTC | 405 |
rs768586972 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827224 | CATTCTAAGTGTATG[A/T]TTTGATGATGTCTAC | 405 |
rs768606880 | snp | G/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876932 | CTCCTTGCGTAAGAG[G/T]TCAATGACCGAGTAA | 405 |
rs768627551 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873400 | TTCTACTTGCCAGTG[A/G]TAAGTAGAACTAGTG | 405 |
rs768633994 | snp | A/G | 1.73042e-05 | 0.00294139 | intron-variant | ARNT | GRCh38.p7 | 1:150816773 | TGTAAAGCAGCACAT[A/G]TATACGGGGCTCACC | 405 |
rs768656271 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868630 | GGGCAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 405 |
rs768709280 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150824605 | GACTAGAGGCGTGCA[A/C]CATCACGCCCAGCTA | 405 |
rs768720779 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817424 | CAATTCTGTTTGCTG[C/T]TGCTGCTGCCTATAT | 405 |
rs768732382 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846096 | CATGTCACCTGAACA[C/T]AAATGATAGTTATAA | 405 |
rs768757898 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844409 | CTACAATGCATTTTA[G/T]GTAATACCCTCTAAT | 405 |
rs768758396 | snp | C/G | 1.65559e-05 | 0.00287709 | intron-variant, missense | ARNT | GRCh38.p7 | 1:150852817 | CCAGCCTGAGGAAAG[C/G]CAACAATAAATACTT | 405 |
rs768770073 | snp | G/T | 1.66103e-05 | 0.00288182 | missense | ARNT | GRCh38.p7 | 1:150813257 | CGATGATGAGGCTGC[G/T]GGCCCTGCCACTGTG | 405 |
rs768772028 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861062 | CACAATGAGAAAGCA[A/T]TTGCTACTCATTAAG | 405 |
rs768777950 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878494 | TAACAAAAATCCCAT[C/T]ATGCTATTGAACAGC | 405 |
rs768796495 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865565 | GAGATGGATTCCTAG[A/G]TCCTTTTCTCTATTC | 405 |
rs768859883 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878756 | GGGAGGCCAAGGAGG[A/G]CGGATCACAAAGTCA | 405 |
rs768879651 | snp | A/G | 8.59867e-05 | 0.00655637 | intron-variant | ARNT | GRCh38.p7 | 1:150813143 | TCTCTCCCAGCTTCT[A/G]ATTTTTGAAAGTCTT | 405 |
rs768884145 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150835286 | GGAAGAACTAGAAAA[A/C]TGAAATCATAAAAAC | 405 |
rs768896641 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150833279 | GAGGCTGACGCAGGC[A/G]AATCACTTGAGGTCA | 405 |
rs768931491 | in-del | -/CACACA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809610 | CGAGACTCCATCTCT[-/CACACA]CACACACACACACAC | 405 |
rs768932097 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810389 | CAACTTTTTGGTTTC[A/G]TAAATTGTGATATAA | 405 |
rs768939476 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852932 | AAAGAGGAAGTGGCA[C/G]AAGTCAAACAAAGCT | 405 |
rs768989095 | snp | A/T | 0.000123617 | 0.00786087 | synonymous-codon, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150876556 | ACCGGGGTTGGCAGT[A/T]GTCGCCGCCATGGCC | 405 |
rs769042801 | snp | C/G | 1.67877e-05 | 0.00289716 | intron-variant | ARNT | GRCh38.p7 | 1:150842494 | AATTAATGAACTAAG[C/G]TAAAATTAAAATAAA | 405 |
rs769091600 | snp | A/G | 1.65048e-05 | 0.00287265 | missense | ARNT | GRCh38.p7 | 1:150829920 | TGCAATCTGCCAATG[A/G]CCACTAGGCAAAACT | 405 |
rs769096175 | snp | A/G/T | 5.03659e-05 | 0.00501805 | synonymous-codon, missense | ARNT | GRCh38.p7 | 1:150846273 | ATTACCTGGCAAACC[A/G/T]CTCCTTATCGTTAGA | 405 |
rs769124411 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150864431 | GGAATACTATGCAGC[C/T]ATAAAAAATGATGAG | 405 |
rs769133439 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150833722 | CCTAAAACGTACAGT[A/C]TATAATTTATAAACA | 405 |
rs769156132 | snp | C/T | | | synonymous-codon, intron-variant | ARNT | GRCh38.p7 | 1:150818009 | GTTGGAGAGTGTAGG[C/T]CGTGGTTCTTGGCTA | 405 |
rs769179391 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809803 | AGTCCCGACTCTTCC[C/G]CTCTCTCCCAAGAAC | 405 |
rs769211473 | snp | A/G | 1.69163e-05 | 0.00290824 | intron-variant | ARNT | GRCh38.p7 | 1:150836239 | TCAGGAAAAAAACAA[A/G]AAAGGACTTCTCATT | 405 |
rs769216355 | snp | C/T | 1.70557e-05 | 0.0029202 | intron-variant | ARNT | GRCh38.p7 | 1:150831797 | TACCAAGGGGAAATA[C/T]TTACTATTTCACTTT | 405 |
rs769225289 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150850030 | GCACTCCAGCCTGGG[A/C]AACAGAGGAAGACTC | 405 |
rs769228896 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150862165 | AGTACTCTGTACTAT[A/G]AATGTATAGTTATGA | 405 |
rs769261575 | in-del | -/TT | | | intron-variant | ARNT | GRCh38.p7 | 1:150849269 | CACACAATCAAATCA[-/TT]TTTTTTTCATTGGGC | 405 |
rs769265724 | snp | C/T | 1.75044e-05 | 0.00295836 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150812000 | TTTTCTCCCCCACCC[C/T]TTATCCTCACCCCAA | 405 |
rs769273005 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150854857 | GCGAAACTACATCTC[-/A]AAAAAAAAAAAAAAA | 405 |
rs769328726 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150852693 | ACAAAAATTTACAAG[C/T]CAGAAGTATAAAGAT | 405 |
rs769353229 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861014 | TGTAAAGTGCTCAAC[A/G]TAACCAATCGCTAGG | 405 |
rs769405315 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150816944 | GGCTGTAGTATATTA[A/G]TTCAGCAAGTTCCTA | 405 |
rs769408900 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877548 | TATTGCCAGCCAAAA[C/T]TGGAGGCAATAGATG | 405 |
rs769411546 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150863355 | ATGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 405 |
rs769452519 | snp | G/T | 1.71959e-05 | 0.00293217 | intron-variant | ARNT | GRCh38.p7 | 1:150816779 | GCAGCACATATATAC[G/T]GGGCTCACCTGAAAT | 405 |
rs769502294 | snp | C/G | 2.05076e-05 | 0.00320209 | intron-variant | ARNT | GRCh38.p7 | 1:150818042 | GTTCCTAGGAAACCA[C/G]AGTAGACAGTAAAGA | 405 |
rs769544350 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825875 | ACTATATAAAATGAA[C/T]TTTTCTACTACAAGC | 405 |
rs769563721 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813532 | TCCAGGCAGCCTTTC[C/T]ATAGAGTTCTTTACT | 405 |
rs769576119 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150833600 | TAATTTCTAGCAACT[A/G]TCCTCTCAGTACAAT | 405 |
rs769609360 | snp | C/G | 1.64882e-05 | 0.00287121 | missense | ARNT | GRCh38.p7 | 1:150829168 | AATGTTGTGTCGGGA[C/G]ATGAACTCTGTTGGT | 405 |
rs769612799 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150855737 | TGAGACCATGTCTTT[-/A]AAAAAAAAAAAAAAA | 405 |
rs769627388 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | ARNT | GRCh38.p7 | 1:150814148 | GTTGGGGCACCAGGG[A/C]GGGACATGGAGCTGA | 405 |
rs769627449 | snp | G/T | 3.31526e-05 | 0.00407127 | intron-variant | ARNT | GRCh38.p7 | 1:150823182 | TTTTTCACACTCCTG[G/T]ATAATACATACTTCA | 405 |
rs769642955 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150842257 | CCCACTTTCTGATGG[C/G]GGAAGCCAAAGTTCC | 405 |
rs769659709 | snp | C/G | 2.36264e-05 | 0.00343695 | missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858385 | CTCTGGACAATGGCT[C/G]CTCCACCTTGAATTC | 405 |
rs769660583 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150868944 | GACCAGCCTGGGCAA[A/C]ATAGCGAGATCCTGT | 405 |
rs769670735 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150844549 | GAGCATCAGCAACGA[A/G]CAAATACTAAGTGCT | 405 |
rs769682172 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150819238 | CAATAAAAAAAAAAA[-/G]GCAATAACAAGTGTT | 405 |
rs769682764 | in-del | -/TA | | | splice-acceptor-variant | ARNT | GRCh38.p7 | 1:150817435 | GCTGTTGCTGCTGCC[-/TA]TATGTCAAAGGCCAG | 405 |
rs769688608 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810058 | GAACTGGAAAGGAAT[A/G]ATAAAGCCGCAATCA | 405 |
rs769712969 | in-del | -/ACTTT | 1.67357e-05 | 0.00289268 | intron-variant | ARNT | GRCh38.p7 | 1:150814265 | TGGAGAGGGGATATA[-/ACTTT]GAACAAATACAGCAT | 405 |
rs769721634 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150866932 | AAATAGAGGCTGGGC[A/G]CAATGGCTCACACTT | 405 |
rs769729276 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | ARNT | GRCh38.p7 | 1:150816872 | GGGACAGTGCTGGAG[A/G]AGATGCCTTTACTCT | 405 |
rs769761614 | snp | C/G | 9.05428e-05 | 0.00672779 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858306 | CAGCAACTAAAGTTG[C/G]TTTATAGGAGAGATA | 405 |
rs769850262 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150841657 | AAAGTCTATGCATAT[C/T]TCTTCTGCAGCATTT | 405 |
rs769870604 | snp | C/G | 7.07977e-05 | 0.00594927 | intron-variant | ARNT | GRCh38.p7 | 1:150813390 | CTACACAATTCCATT[C/G]TGTACTAATGCCACA | 405 |
rs769898123 | in-del | -/GA | 0.000374625 | 0.0136811 | intron-variant | ARNT | GRCh38.p7 | 1:150818082 | GAGGGAGGAAGGGGG[-/GA]GAGAGAGAGAAAGAG | 405 |
rs769905221 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813919 | GCGTGAGCCACCGCA[C/T]CCAGCTGGTAGGTTT | 405 |
rs769977222 | snp | C/T | 1.68707e-05 | 0.00290432 | intron-variant | ARNT | GRCh38.p7 | 1:150826645 | AAGAAGAGTAAGATA[C/T]ATACTTTTTTTTTTT | 405 |
rs769991426 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150842144 | TTCTAAGAGCTTTTT[A/G]TTCTGTGAAACTTAG | 405 |
rs770011429 | in-del | -/AAAAAAAA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809641 | CACACACACAAAAAA[-/AAAAAAAA]AAAAAAAAGTTGCTA | 405 |
rs770026934 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | ARNT | GRCh38.p7 | 1:150839414 | ACCCAGATTCCAGAC[C/T]CTCTCAGAACTATAA | 405 |
rs770086013 | snp | C/T | 1.65222e-05 | 0.00287417 | synonymous-codon | ARNT | GRCh38.p7 | 1:150852779 | CAAAAATTTACTGTT[C/T]CCTTCTCCATCATCA | 405 |
rs770165634 | snp | G/T | 1.65605e-05 | 0.0028775 | missense | ARNT | GRCh38.p7 | 1:150831827 | TCTTACCTGCTGGGG[G/T]CCAGGCCTTGATGTA | 405 |
rs770198524 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868760 | CAAAAATTAGCCAGG[C/T]GCGGTGGCACGTGCC | 405 |
rs770206803 | snp | A/G | | | missense | ARNT | GRCh38.p7 | 1:150839530 | GAGAAACTGCCATGC[A/G]TAAGATGGTTAGCTT | 405 |
rs770218451 | snp | A/C/T | 4.94379e-05 | 0.00497161 | intron-variant | ARNT | GRCh38.p7 | 1:150817332 | AGTAAATACTCCCTA[A/C/T]CCTCTTCAACGAAGA | 405 |
rs770226120 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849663 | AGCTACTTGGGAGAC[C/T]GAGGTGGGAGGATCG | 405 |
rs770228784 | snp | A/C | 1.64817e-05 | 0.00287064 | intron-variant | ARNT | GRCh38.p7 | 1:150832284 | TAAAAATGTGATGAT[A/C]TCTGCAGGTATTTGG | 405 |
rs770229886 | in-del | -/ACACAT/ACAT | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811481 | CACACACACACATAC[-/ACACAT/ACAT]ACACACACTCTCTCT | 405 |
rs770234321 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150831417 | TCTTTGCAGAGAATA[C/T]CCTCTTGATAAGTTA | 405 |
rs770313697 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867861 | CTATCCTGCCAGCCA[C/T]GTGAAGACATGCTTG | 405 |
rs770349122 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150848779 | TTAAGCGATCCACCC[A/G]CCTCAGCCTCCTAAA | 405 |
rs770370352 | snp | C/T | 3.30028e-05 | 0.00406205 | missense | ARNT | GRCh38.p7 | 1:150823200 | AATACATACTTCACA[C/T]TGGTGTTGGTACAGA | 405 |
rs770390109 | snp | A/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877457 | TGGTGAAAAAGTTAA[A/T]TGACTAACTTTTGAA | 405 |
rs770452617 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150814771 | TCACTTGAACCCGGG[A/G]GACAGAGGTTGCAGT | 405 |
rs770473525 | snp | A/C | 0.000154787 | 0.00879599 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876581 | ATGGCCGCAGATGCC[A/C]CCGCCGCCGCGCCAC | 405 |
rs770540371 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150830856 | ATAGAGGTATGAAAG[A/T]TCACATACTTTAACT | 405 |
rs770566546 | in-del | -/A | 1.71852e-05 | 0.00293127 | intron-variant | ARNT | GRCh38.p7 | 1:150842507 | AGCTAAAATTAAAAT[-/A]AAAAAGAAGGAAGGA | 405 |
rs770616033 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150828381 | GCATACAGATATCCA[A/G]TTGTTCCATTTGTTA | 405 |
rs770642997 | snp | A/C | 1.64808e-05 | 0.00287057 | intron-variant | ARNT | GRCh38.p7 | 1:150816237 | AATAATACACAGGGA[A/C]CACACAGATGATAAG | 405 |
rs770667352 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150813930 | CGCACCCAGCTGGTA[A/G]GTTTTAAATTCTAAA | 405 |
rs770668693 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840524 | GGCAGAATTTGAAGA[C/T]TTTGAAGTTTTATTT | 405 |
rs770675326 | snp | C/T | 5.02727e-05 | 0.00501337 | missense | ARNT | GRCh38.p7 | 1:150816329 | GTGGGGTTGGAGTGG[C/T]GGGAAATCTGGGCCA | 405 |
rs770704128 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150842023 | GTGTGGAGTAAATGC[C/T]GAGGCCTAAATACTG | 405 |
rs770731267 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150848428 | ACCACTGCACTCCAA[C/T]GTGGGCAACAAGAGC | 405 |
rs770745835 | snp | C/T | 2.26734e-05 | 0.00336693 | missense, synonymous-codon, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858401 | CTCCACCTTGAATTC[C/T]AGGTCCAGAGTTTCC | 405 |
rs770751257 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852440 | AATGCAGTCTTATGA[C/G]TGAGTCTAGGTGAGA | 405 |
rs770779838 | in-del | -/T | 0.00587572 | 0.0538826 | intron-variant | ARNT | GRCh38.p7 | 1:150826649 | GAGTAAGATATATAC[-/T]TTTTTTTTTTTTAAG | 405 |
rs770843265 | snp | C/T | 1.65886e-05 | 0.00287993 | intron-variant | ARNT | GRCh38.p7 | 1:150836266 | CATTCATTTCCCATA[C/T]ACATAACTCTCACCT | 405 |
rs770854087 | in-del | -/AA/AAA | | | intron-variant | ARNT | GRCh38.p7 | 1:150874018 | ACTAACAAGAATTGT[-/AA/AAA]AAAAAAAAAAAAAAA | 405 |
rs770943007 | snp | C/G | 5.06278e-05 | 0.00503104 | intron-variant | ARNT | GRCh38.p7 | 1:150818069 | AAGAGGGGGTGGAGA[C/G]GGAGGAAGGGGGGAG | 405 |
rs770948263 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150837301 | TATTCACTGGCTTTA[G/T]CCTCTTACCTTTCAA | 405 |
rs771071960 | snp | A/G | 1.66098e-05 | 0.00288177 | intron-variant | ARNT | GRCh38.p7 | 1:150839702 | TGGTCACATCTGGTC[A/G]TTTGGTAGCAGGGAG | 405 |
rs771165852 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853523 | AACATCTTTCAAAGC[A/T]GTGATCTTACATAAA | 405 |
rs771167160 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150818159 | TGGAACAATCAATAA[A/G]TCCTTCATTAAAGTC | 405 |
rs771218519 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150821302 | AAGACTTCCAGCATC[A/G]CTAGTGGCACTTCAT | 405 |
rs771221579 | snp | A/G | 1.65244e-05 | 0.00287436 | synonymous-codon | ARNT | GRCh38.p7 | 1:150829222 | ACAGTTGGGAGAACT[A/G]GTTACCTGAGAGTGA | 405 |
rs771279928 | snp | C/G | 2.98619e-05 | 0.00386394 | intron-variant | ARNT | GRCh38.p7 | 1:150817896 | GGTGACTGCTCAACA[C/G]ATGATTATTTCACCC | 405 |
rs771340877 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821265 | TTTCTTATAATGTCA[A/T]GACTTTTCCCTGCTT | 405 |
rs771346355 | snp | A/G | 1.64931e-05 | 0.00287163 | intron-variant | ARNT | GRCh38.p7 | 1:150816906 | CTGTGGACCAAAAGG[A/G]GTTGGGGAAGGGCCA | 405 |
rs771348484 | snp | C/T | 3.31203e-05 | 0.00406928 | intron-variant | ARNT | GRCh38.p7 | 1:150829861 | AGTCCTGAAGATCTG[C/T]TCTAATTGAACGGGA | 405 |
rs771356459 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867706 | ATCCCCAGTGTTGAA[G/T]GTGCAGTCTGGTGGG | 405 |
rs771357844 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150844800 | CTTGTCACAAAAACT[A/G]TTTCCTTACTGTCTT | 405 |
rs771358584 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150846679 | GTACAGTTGAGTAGT[C/G]CTAACCATATTCACA | 405 |
rs771390470 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | ARNT | GRCh38.p7 | 1:150839508 | GTTCCCCGCAAGGAC[C/T]TCATGTGAGAAACTG | 405 |
rs771391161 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860026 | AAAAAAAAGGGTGCA[C/T]TTTTCTCTTAGTAAA | 405 |
rs771464000 | snp | A/G | 1.65048e-05 | 0.00287265 | synonymous-codon | ARNT | GRCh38.p7 | 1:150816358 | CAACATCTGTCCTGC[A/G]GAAGCTGATGGCTGG | 405 |
rs771485206 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866762 | ACCCAGATAAACACA[G/T]AAAAAATAAAATCCA | 405 |
rs771486074 | snp | A/G | 1.67077e-05 | 0.00289026 | intron-variant | ARNT | GRCh38.p7 | 1:150814039 | TTTCTCTTTAGTGGT[A/G]CGATTTTCCTGTTAC | 405 |
rs771511711 | in-del | -/TT | | | intron-variant | ARNT | GRCh38.p7 | 1:150831313 | AAGCCAACTTAAAAC[-/TT]TGATCCTGCAACCCA | 405 |
rs771515866 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838429 | CACAGCACAACACAC[C/T]TGGTTTGCCCACAAA | 405 |
rs771518527 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150828767 | CCATTATTCATTTAG[A/G]TAATTACATGAATTA | 405 |
rs771524690 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150866773 | CACATAAAAAATAAA[A/C]TCCAAACACTTATAG | 405 |
rs771524947 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150842476 | CATCCGACCTAAAAA[C/T]AGAATTAATGAACTA | 405 |
rs771566102 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150817700 | TGTAATCCCAGCTAT[C/T]TGGGAGGCTGAGGCA | 405 |
rs771570695 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873506 | TAGAGAGTACCAACC[A/G]TATTTTACTCTTCTT | 405 |
rs771575558 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878324 | GCAAGGGACATCCAG[C/T]AGGTAAGTAATGTGG | 405 |
rs771607324 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820946 | TAAACTTCTGACTCT[C/T]CCAAAACGTTACTAC | 405 |
rs771636640 | in-del | -/TTT | | | intron-variant | ARNT | GRCh38.p7 | 1:150828351 | GTGGTTTTTTTTTTG[-/TTT]TTTTTTTTTTTTGCA | 405 |
rs771648428 | snp | C/T | 3.39397e-05 | 0.00411931 | intron-variant | ARNT | GRCh38.p7 | 1:150846356 | TACACTTGTTATATC[C/T]ATTTCACTCTGAAAA | 405 |
rs771672355 | in-del | -/T | 1.71852e-05 | 0.00293127 | intron-variant | ARNT | GRCh38.p7 | 1:150813145 | TCTCCCAGCTTCTAA[-/T]TTTTGAAAGTCTTTT | 405 |
rs771712365 | snp | A/G | 1.67452e-05 | 0.0028935 | intron-variant | ARNT | GRCh38.p7 | 1:150846318 | CACACCTGAAGGAGA[A/G]AAAAAGGATTGTTTC | 405 |
rs771775299 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150866485 | GTCTTTCACTGGGAC[A/G]CTTTATTTAAACAGA | 405 |
rs771799495 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | ARNT | GRCh38.p7 | 1:150832304 | CAGGTATTTGGCCAT[C/T]CCTTTGGTTTTCACC | 405 |
rs771835083 | snp | C/T | 1.65321e-05 | 0.00287502 | missense | ARNT | GRCh38.p7 | 1:150852802 | CATCATCATCAAAAT[C/T]CAGCCTGAGGAAAGC | 405 |
rs771862677 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150850235 | TACTAAAAATACAAA[A/T]ATTAGCCCTCTCCCT | 405 |
rs771882487 | snp | A/G | 1.65269e-05 | 0.00287457 | missense | ARNT | GRCh38.p7 | 1:150836406 | AAACAGGAGTCACGG[A/G]GTCAGACACATACAC | 405 |
rs771900252 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851402 | TGATGACGATGGCGG[-/T]TTTGTCGAATAGAAA | 405 |
rs771922743 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811632 | ATTTCTCCTCTCCTC[C/T]ACTCTCTTCAGAATT | 405 |
rs771928461 | snp | A/G | 0.000117254 | 0.00765593 | intron-variant | ARNT | GRCh38.p7 | 1:150876518 | CCCTCCCCTTTAGAG[A/G]CGCCCCAGTCCTCCG | 405 |
rs771935569 | snp | C/T | 2.56974e-05 | 0.00358441 | intron-variant | ARNT | GRCh38.p7 | 1:150836527 | TAGAAGTTAATATTT[C/T]ACTCTGAAAAAACAA | 405 |
rs771941807 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | ARNT | GRCh38.p7 | 1:150823210 | TCACATTGGTGTTGG[C/T]ACAGATGATGTACTC | 405 |
rs771947287 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838932 | ATACTTATATTCAGA[C/T]GAAGTTCCTGAAAGG | 405 |
rs772057438 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857092 | ACTATTACCCAGAAA[C/T]GTGGTATATATTCTT | 405 |
rs772104958 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868644 | CGGTGGCTCACGCCT[C/G]TAATCCCAGCACTTT | 405 |
rs772199454 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150870611 | CTCCCAGGCTCAGGT[C/G]ATCCTCGCATCTCAG | 405 |
rs772220628 | snp | G/T | 3.3106e-05 | 0.0040684 | intron-variant | ARNT | GRCh38.p7 | 1:150829873 | CTGCTCTAATTGAAC[G/T]GGAATATAGATGTGG | 405 |
rs772229076 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150822262 | GGAATCTTCAGTGTG[A/G]TAAGTGTCTTTTTGT | 405 |
rs772256793 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865352 | TTTTGAAACTAGAGA[C/T]AAAATGGACTATTGC | 405 |
rs772297860 | snp | C/T | 5.92177e-05 | 0.00544108 | splice-acceptor-variant, intron-variant | ARNT | GRCh38.p7 | 1:150818032 | CTTGGCTAGAGTTCC[C/T]AGGAAACCAGAGTAG | 405 |
rs772297869 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819614 | ATACATGCTACAACA[C/T]GTATCAGTACAGATA | 405 |
rs772319934 | in-del | -/AAGGA | 1.65844e-05 | 0.00287957 | intron-variant | ARNT | GRCh38.p7 | 1:150852738 | TAATATCAGACATCT[-/AAGGA]AAGTTTTTCAGTCTC | 405 |
rs772356330 | snp | A/G | 1.64852e-05 | 0.00287094 | missense | ARNT | GRCh38.p7 | 1:150817097 | CCGCATTGATGTTGT[A/G]ATAGATTTCTGAAAA | 405 |
rs772424650 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150825580 | TCTAGGCTGGGCGCA[A/G]TGGCTCATGCCTGTA | 405 |
rs772437102 | in-del | -/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878237 | ACTCATTTAATCCTC[-/T]ACAACAACGATGAGG | 405 |
rs772442430 | snp | C/T | 1.66161e-05 | 0.00288232 | intron-variant | ARNT | GRCh38.p7 | 1:150842383 | GGATAGAAAAAGCAG[C/T]ATCATCTGCTTCATC | 405 |
rs772458027 | snp | G/T | 1.67027e-05 | 0.00288982 | intron-variant | ARNT | GRCh38.p7 | 1:150814041 | TCTCTTTAGTGGTGC[G/T]ATTTTCCTGTTACTC | 405 |
rs772477454 | snp | A/G | 1.65113e-05 | 0.00287322 | intron-variant | ARNT | GRCh38.p7 | 1:150817222 | GGAATACAATGATAA[A/G]AATAACCATTAAAGA | 405 |
rs772551495 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150818478 | AATACTGGCCAGGCA[C/T]GGTGGCTTACACCTG | 405 |
rs772608216 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840737 | GAATCTCACCCAGGT[A/G]AATAGACCACAGCTC | 405 |
rs772615661 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150873659 | GTCAGTGGCTCACAC[C/T]TATAATCCCAGCAGT | 405 |
rs772643116 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150835618 | TTGGGTGGGAAAAAA[G/T]GAGGAAAACTAAAGA | 405 |
rs772648016 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150812848 | AAATGGTATGTATCA[C/T]ACTCAATTCATACTC | 405 |
rs772671761 | snp | A/G | 1.66682e-05 | 0.00288684 | intron-variant | ARNT | GRCh38.p7 | 1:150842478 | TCCGACCTAAAAATA[A/G]AATTAATGAACTAAG | 405 |
rs772714484 | in-del | -/CTA | | | intron-variant | ARNT | GRCh38.p7 | 1:150843931 | CTAAAATTCCTATTT[-/CTA]CTACTACTACTACTA | 405 |
rs772733665 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811597 | ACCTACAATGTTTCA[C/T]GGTCCTCAAATATGA | 405 |
rs772739409 | snp | C/T | 1.67198e-05 | 0.0028913 | intron-variant | ARNT | GRCh38.p7 | 1:150836253 | AGAAAGGACTTCTCA[C/T]TCATTTCCCATACAC | 405 |
rs772779252 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150821015 | TAAGCAGTTGAACAC[A/G]TTTTGTATGTTGTAC | 405 |
rs772808088 | snp | A/G | 6.91085e-05 | 0.00587788 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150817969 | GTAAATTAGCTGTGG[A/G]ACCTAGTTGTGGCCT | 405 |
rs772828102 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150822175 | TCACAAATATCAAAA[G/T]AATTTTCTAATATAT | 405 |
rs772878610 | snp | A/T | 1.66178e-05 | 0.00288247 | intron-variant | ARNT | GRCh38.p7 | 1:150842390 | AAAAGCAGCATCATC[A/T]GCTTCATCATGCTAA | 405 |
rs772897717 | snp | C/G | 1.6483e-05 | 0.00287076 | missense | ARNT | GRCh38.p7 | 1:150816888 | AGATGCCTTTACTCT[C/G]ATCTGTGGACCAAAA | 405 |
rs772934181 | in-del | -/ACAGC | 1.68136e-05 | 0.0028994 | intron-variant | ARNT | GRCh38.p7 | 1:150814274 | GGATATAGAACAAAT[-/ACAGC]ATTAACATCATTGCA | 405 |
rs772948366 | snp | C/T | 4.4606e-05 | 0.0047224 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858311 | ACTAAAGTTGGTTTA[C/T]AGGAGAGATATTCAT | 405 |
rs772992999 | snp | C/G | 1.64738e-05 | 0.00286995 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814168 | CATGGAGCTGAAGGA[C/G]GATGGAGTCTGAAAG | 405 |
rs773003428 | snp | A/C | 1.64811e-05 | 0.00287059 | synonymous-codon | ARNT | GRCh38.p7 | 1:150834639 | TAGATCCAGGATACG[A/C]CCTGAAGGAAGATGT | 405 |
rs773003767 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150870714 | GGGTTTCACCACGTT[A/G]CCCAGGCTGGTCTCA | 405 |
rs773016515 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819551 | ACAGTATGTGGTATA[-/T]TCCATACAATGAAAT | 405 |
rs773026334 | in-del | -/AT | 1.67298e-05 | 0.00289217 | intron-variant | ARNT | GRCh38.p7 | 1:150823378 | CCATCAGTGGAACTC[-/AT]AGAAAATTTTCATTA | 405 |
rs773046037 | snp | A/C | 1.64833e-05 | 0.00287078 | intron-variant | ARNT | GRCh38.p7 | 1:150816232 | CAAAAAATAATACAC[A/C]GGGAACACACAGATG | 405 |
rs773060428 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150850153 | AGCACTTTGGGAGGC[C/T]GAGGAGGGCGGATCA | 405 |
rs773125354 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150814561 | ATATGCAGGCCAGGC[A/G]GGGTGGCTCATGGCT | 405 |
rs773169055 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815162 | GACTTTTTAAAACTA[C/T]TACTTGTATAACATA | 405 |
rs773179687 | snp | C/T | 6.95676e-05 | 0.00589737 | missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858391 | ACAATGGCTCCTCCA[C/T]CTTGAATTCCAGGTC | 405 |
rs773194024 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878083 | TCCCTCCCGGGTTCA[A/G]GCAGTTATCCTGCCT | 405 |
rs773220436 | snp | C/T | 6.61912e-05 | 0.0057525 | intron-variant | ARNT | GRCh38.p7 | 1:150826505 | ATGGAGTGAATATGA[C/T]AAATATTTATTCAGA | 405 |
rs773231217 | snp | A/G | 1.6492e-05 | 0.00287154 | missense | ARNT | GRCh38.p7 | 1:150813284 | TGTGGCCAGACACCC[A/G]CACCCTCTGCTGTCC | 405 |
rs773265076 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857523 | AACCCAAGCATCACT[C/T]TTCCATTACTATTGG | 405 |
rs773315761 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853194 | GCTGAGGCAGGAGAA[C/T]TGCTGGAACCCGGGA | 405 |
rs773376101 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868857 | GAGCCGAGATCACGC[C/T]ACTGCACTCCAGCCT | 405 |
rs773382299 | snp | A/G | 0.000430072 | 0.0146578 | synonymous-codon | ARNT | GRCh38.p7 | 1:150831831 | ACCTGCTGGGGGCCA[A/G]GCCTTGATGTAGCCT | 405 |
rs773429506 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150870618 | GCTCAGGTCATCCTC[A/G]CATCTCAGTCTCCCA | 405 |
rs773484109 | snp | C/T | 1.64743e-05 | 0.00287 | missense | ARNT | GRCh38.p7 | 1:150839490 | TCAGTGGATGTGTTG[C/T]CAGTTCCCCGCAAGG | 405 |
rs773522371 | in-del | -/CA | | | intron-variant | ARNT | GRCh38.p7 | 1:150859375 | TTTAAGACAGGGTCT[-/CA]CTTTGTCCAGCCCAG | 405 |
rs773535220 | snp | G/T | 3.26974e-05 | 0.00404322 | intron-variant | ARNT | GRCh38.p7 | 1:150826650 | GAGTAAGATATATAC[G/T]TTTTTTTTTTTAAGA | 405 |
rs773550155 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868761 | AAAAATTAGCCAGGC[A/G]CGGTGGCACGTGCCT | 405 |
rs773558363 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150856635 | GGGCGTGGTGGCGCA[C/T]GCCTGTAGTCCCAGC | 405 |
rs773563586 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810031 | CTCTGGTTGTGGGTG[C/T]CTGTTGTTTATGAAC | 405 |
rs773575539 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810053 | TTTATGAACTGGAAA[C/G]GAATGATAAAGCCGC | 405 |
rs773644471 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819754 | AGATTCATAGTTATA[C/T]AGAATTTCAGAGCCG | 405 |
rs773696724 | snp | G/T | 1.65042e-05 | 0.0028726 | missense | ARNT | GRCh38.p7 | 1:150814226 | GTCTTAGCAGTAGCC[G/T]GGGTAGCCACCTGCT | 405 |
rs773699943 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150826269 | GCGCATGAGCCACCA[C/T]GCCTGGCGCAATAGT | 405 |
rs773796157 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827225 | ATTCTAAGTGTATGA[C/T]TTGATGATGTCTACT | 405 |
rs773853379 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150844859 | CTGTCACCCAGGCTG[A/G]AGTGCAATGGTGCCA | 405 |
rs773854292 | snp | C/G | 1.6686e-05 | 0.00288838 | missense | ARNT | GRCh38.p7 | 1:150846292 | CTTATCGTTAGACAT[C/G]TGATCATCATCACAC | 405 |
rs773878322 | snp | C/T | 0.000154548 | 0.00878919 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876582 | TGGCCGCAGATGCCA[C/T]CGCCGCCGCGCCACC | 405 |
rs773925763 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150875781 | ATTTTTTGAAATTGA[A/G]AAATGGTGTGGAATC | 405 |
rs773926365 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant | ARNT | GRCh38.p7 | 1:150816239 | TAATACACAGGGAAC[A/G]CACAGATGATAAGTT | 405 |
rs773979347 | snp | C/T | 7.20279e-05 | 0.00600073 | intron-variant | ARNT | GRCh38.p7 | 1:150846213 | GACTGTCTGGTTCTA[C/T]AACATGGATCATATT | 405 |
rs774021972 | snp | G/T | 3.43477e-05 | 0.00414399 | missense | ARNT | GRCh38.p7 | 1:150812024 | ACCCCAATAGTTCTA[G/T]TCTGAAAAGGGGGGA | 405 |
rs774049938 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853306 | AAGTACAAAACTGGG[C/T]AATAGAAACAAAAGT | 405 |
rs774073465 | snp | A/G | 2.25573e-05 | 0.0033583 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858411 | AATTCCAGGTCCAGA[A/G]TTTCCAGAGGCAATG | 405 |
rs774081222 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150848066 | TAAAAAAAACTGAGG[-/A]AGATAAGTGTGTGTA | 405 |
rs774092878 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150862530 | CAGCCTATAAATTTG[A/T]AATAGTAAGCATATG | 405 |
rs774133350 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150823075 | GCACATGCCACCACG[C/G]CCGGCTAAATTTTTG | 405 |
rs774134316 | snp | A/C | 2.71381e-05 | 0.00368352 | intron-variant | ARNT | GRCh38.p7 | 1:150818075 | GGGTGGAGAGGGAGG[A/C]AGGGGGGAGAGAGAG | 405 |
rs774139789 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150850101 | GCTCCAGAATATTAA[-/C]AACTCAAAAATACAA | 405 |
rs774151563 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820062 | CAAATCAGGCCCACT[A/G]CCTGTTTTTCTAAAT | 405 |
rs774198178 | snp | A/G | 1.65792e-05 | 0.00287912 | intron-variant | ARNT | GRCh38.p7 | 1:150836267 | ATTCATTTCCCATAC[A/G]CATAACTCTCACCTG | 405 |
rs774222894 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150837909 | TTAACAGCATCCTCC[C/T]AAGCTAGAAGCCTCA | 405 |
rs774226596 | snp | C/T | 3.40072e-05 | 0.0041234 | intron-variant | ARNT | GRCh38.p7 | 1:150839704 | GTCACATCTGGTCAT[C/T]TGGTAGCAGGGAGAG | 405 |
rs774247572 | snp | C/T | 0.000181808 | 0.00953262 | missense | ARNT | GRCh38.p7 | 1:150836403 | TCAAAACAGGAGTCA[C/T]GGAGTCAGACACATA | 405 |
rs774270176 | in-del | -/ATC | 1.79728e-05 | 0.00299768 | intron-variant | ARNT | GRCh38.p7 | 1:150846221 | GGTTCTACAACATGG[-/ATC]ATATTATATATTACA | 405 |
rs774319652 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150855493 | CATGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 405 |
rs774372483 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150835439 | CAGAACCTGTCTCTA[-/C]AAAAAATTTAAAAAT | 405 |
rs774377664 | in-del | -/TT | 0.000574414 | 0.0169374 | intron-variant | ARNT | GRCh38.p7 | 1:150826650 | GAGTAAGATATATAC[-/TT]TTTTTTTTTTAAGAT | 405 |
rs774499564 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871003 | GAGACCCGGTCACTA[C/T]CTAAAATAATAAAAA | 405 |
rs774507897 | snp | C/T | 6.71479e-05 | 0.00579391 | intron-variant | ARNT | GRCh38.p7 | 1:150829049 | TACATAATGTCAACA[C/T]AGCCAAAGGAAAATG | 405 |
rs774542268 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150864723 | CATATGTAACTAACC[C/T]GCACAATGTGCACAT | 405 |
rs774544024 | snp | C/G | 3.30006e-05 | 0.00406192 | intron-variant | ARNT | GRCh38.p7 | 1:150817454 | TGTCAAAGGCCAGTT[C/G]ACAAGACAAATAGAA | 405 |
rs774564669 | snp | A/C | 0.00666342 | 0.0573351 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876598 | CGCCGCCGCGCCACC[A/C]CCCCCCCCAGTGGGA | 405 |
rs774581935 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150863244 | GTACACGTCTATAAT[A/C]CCAGCTACTTGGGAG | 405 |
rs774632636 | snp | C/G | 1.67142e-05 | 0.00289081 | intron-variant | ARNT | GRCh38.p7 | 1:150829264 | TGAGGTAAAATGATA[C/G]CATTATTTACAGATG | 405 |
rs774646032 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810251 | AAAGCAAAAACAAAA[C/T]CCCCAGAGCATCTTC | 405 |
rs774652296 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877845 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACATCAG | 405 |
rs774693239 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150834024 | ACTGCAACCTCCACC[A/T]CCTGGGTTCAAGCAA | 405 |
rs774709554 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828192 | GAATCATGCTTTTAG[G/T]GTAAGAAATCTTTTG | 405 |
rs774712704 | snp | G/T | 4.95193e-05 | 0.00497566 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813295 | ACCCACACCCTCTGC[G/T]GTCCGTGTCTGGAAT | 405 |
rs774767100 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150850041 | TGGGCAACAGAGGAA[A/G]ACTCTGTCTCAAAAA | 405 |
rs774794911 | snp | C/T | 5.8713e-05 | 0.00541785 | intron-variant | ARNT | GRCh38.p7 | 1:150817898 | TGACTGCTCAACAGA[C/T]GATTATTTCACCCTT | 405 |
rs774797290 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878757 | GGAGGCCAAGGAGGG[C/T]GGATCACAAAGTCAG | 405 |
rs774799661 | snp | A/G | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811129 | CAGCCTATTTAGGTA[A/G]TGTTTGCAGATCTTC | 405 |
rs774811755 | snp | C/T | 0.0016824 | 0.0289546 | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861264 | GTAGTCCCAGCTACT[C/T]GGGGTCTGAGGCAGG | 405 |
rs774837278 | snp | A/C/T | 5.01629e-05 | 0.00500793 | intron-variant | ARNT | GRCh38.p7 | 1:150814040 | TTCTCTTTAGTGGTG[A/C/T]GATTTTCCTGTTACT | 405 |
rs774907401 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150833365 | AAAATTAGCCAGCTG[C/T]GGTGGCAATCCAGCT | 405 |
rs774944295 | snp | A/C | 1.64735e-05 | 0.00286993 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839519 | GGACTTCATGTGAGA[A/C]ACTGCCATGCGTAAG | 405 |
rs774958612 | in-del | -/AAAAC | | | intron-variant | ARNT | GRCh38.p7 | 1:150820668 | CTGAAAAAACAAAAC[-/AAAAC]AAAACAAAACAAAAC | 405 |
rs774985804 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | ARNT | GRCh38.p7 | 1:150832323 | TTGGTTTTCACCACT[C/T]AGGATCTCACCTGCA | 405 |
rs775013426 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150862326 | TCTGATTGCCCATTA[C/T]CTGCCAAGGAGGTTA | 405 |
rs775019737 | snp | G/T | 1.65138e-05 | 0.00287343 | missense | ARNT | GRCh38.p7 | 1:150816369 | CTGCAGAAGCTGATG[G/T]CTGGACAATGGTTAC | 405 |
rs775028030 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150823803 | GATCCGCCCGCCTCG[G/T]CCTCCCAAAGTGCTG | 405 |
rs775038694 | in-del | -/TGG | | | intron-variant | ARNT | GRCh38.p7 | 1:150828525 | AACACCACAGTGTCT[-/TGG]TAATAGCTTTATAGT | 405 |
rs775079516 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150869118 | TGGCTGACACAACAG[C/G]ACCTTGTCTCAAAAA | 405 |
rs775080347 | snp | C/T | 3.35413e-05 | 0.00409506 | intron-variant | ARNT | GRCh38.p7 | 1:150846327 | AGGAGAGAAAAAGGA[C/T]TGTTTCAAAGCATTA | 405 |
rs775081803 | snp | A/C | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811179 | AAAAGCAGCAGTAAC[A/C]CAGCTTTATCACTGA | 405 |
rs775171579 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150826937 | CAGGTGTGAGCCACC[A/G]TGCCCAGCCAACATA | 405 |
rs775324499 | snp | A/T | 1.6483e-05 | 0.00287076 | missense | ARNT | GRCh38.p7 | 1:150823216 | TGGTGTTGGTACAGA[A/T]GATGTACTCAATTTC | 405 |
rs775388830 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | ARNT | GRCh38.p7 | 1:150829889 | GGAATATAGATGTGG[A/G]AAATTCATACTTGCC | 405 |
rs775418607 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150845859 | GTGAGCCGAGATGGC[A/G]CCATTGCACTCCAGC | 405 |
rs775432368 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854687 | CATGGTGAAACCTCG[C/T]CTCTACTAAAAATAC | 405 |
rs775435499 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868949 | GCCTGGGCAACATAG[C/T]GAGATCCTGTCTCTA | 405 |
rs775442173 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817107 | GTTGTGATAGATTTC[C/T]GAAAATCTTGGATCT | 405 |
rs775584384 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860505 | ACAGGCATGAGCCAC[C/T]GTGCCCAGCAGAAAA | 405 |
rs775596380 | in-del | -/T | 1.65272e-05 | 0.0028746 | intron-variant | ARNT | GRCh38.p7 | 1:150829893 | TATAGATGTGGAAAA[-/T]TCATACTTGCCTGCA | 405 |
rs775662276 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821696 | CTCTGTCACCCAGGC[A/T]GGAGTGCAGTGGTGC | 405 |
rs775666944 | snp | C/T | 1.6582e-05 | 0.00287936 | intron-variant | ARNT | GRCh38.p7 | 1:150814059 | TTTCCTGTTACTCTC[C/T]TTATGGTCTGGACTC | 405 |
rs775708945 | snp | C/G | 1.65282e-05 | 0.00287469 | missense | ARNT | GRCh38.p7 | 1:150836282 | ACATAACTCTCACCT[C/G]TCAGGGCATTTTCTG | 405 |
rs775719165 | in-del | -/AATACAAAACATTAA | 1.69231e-05 | 0.00290882 | intron-variant | ARNT | GRCh38.p7 | 1:150852845 | TTTAAGCCTGCTGAT[-/AATACAAAACATTAA]AATACAAAACATTAA | 405 |
rs775752139 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838826 | TCCCTTCAGTATGTC[C/T]ATCTAGTCCCACATA | 405 |
rs775784543 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150860141 | AGTTCATACTGTATA[-/G]TGTACAATATTTTGT | 405 |
rs775799292 | snp | C/G | 0.000275824 | 0.0117404 | intron-variant | ARNT | GRCh38.p7 | 1:150861231 | TAAAAATAAAACTGG[C/G]TGCAGTGGTGCGCAC | 405 |
rs775824664 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150822993 | ATGATCCCAGCTCAC[C/T]GCAACCTCCACCTCT | 405 |
rs775849120 | snp | A/C | 1.67961e-05 | 0.00289789 | synonymous-codon | ARNT | GRCh38.p7 | 1:150812054 | AAACATAGTTAGATC[A/C]GGGAATTCTTCATTG | 405 |
rs775894926 | snp | G/T | 3.32325e-05 | 0.00407617 | intron-variant | ARNT | GRCh38.p7 | 1:150842385 | ATAGAAAAAGCAGCA[G/T]CATCTGCTTCATCAT | 405 |
rs775902596 | snp | A/T | 1.73036e-05 | 0.00294134 | intron-variant | ARNT | GRCh38.p7 | 1:150813122 | CTCTCCTCCTCCTGG[A/T]CCCTTTCTCTCCCAG | 405 |
rs775912908 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150864917 | AAAGAAAAAGACCTA[C/T]AAAAGGTAAGATGTC | 405 |
rs775923893 | snp | A/C/G | 3.29469e-05 | 0.00405864 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814147 | AGTTGGGGCACCAGG[A/C/G]AGGGACATGGAGCTG | 405 |
rs775941149 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150833607 | TAGCAACTATCCTCT[C/G]AGTACAATGTAGTCA | 405 |
rs775973216 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150831604 | GTGACACAGCCAATA[-/C]TGAATCATTTTCCAG | 405 |
rs776026652 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150814866 | ACAACAAAAAAAGTA[C/T]CATATGCAGAGAAAA | 405 |
rs776030922 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857942 | TCTGCATTCCAAACC[A/T]AGCAACATATCAATA | 405 |
rs776046513 | snp | C/T | 3.35869e-05 | 0.00409784 | intron-variant | ARNT | GRCh38.p7 | 1:150829278 | ACCATTATTTACAGA[C/T]GTATTTCCTATCTCC | 405 |
rs776139350 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150822123 | ATTTTTTCAATATAT[C/T]CAGGCTATGTAGCTT | 405 |
rs776142075 | snp | A/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877482 | TTTGAATGCCTGCTA[A/T]GGAACCGGTAGTCTA | 405 |
rs776202425 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150875613 | CAAGATAAACTAGAC[C/T]CCTAAAATGAAATGC | 405 |
rs776284140 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878442 | CCATTTTCATGTATC[A/G]CTCACAAAATGTTTA | 405 |
rs776342524 | snp | C/T | 3.29522e-05 | 0.00405894 | missense | ARNT | GRCh38.p7 | 1:150834617 | CCTTTTTCACTGTTC[C/T]AGTCTTTAGATCCAG | 405 |
rs776388663 | snp | C/T | 1.81059e-05 | 0.00300876 | synonymous-codon, intron-variant | ARNT | GRCh38.p7 | 1:150817946 | CTGTCCTGAGCCCAT[C/T]TCCAGGGGTAAATTA | 405 |
rs776401333 | snp | A/C/T | 0.000211663 | 0.0102853 | intron-variant | ARNT | GRCh38.p7 | 1:150829542 | TAACCAAGAAACTTA[A/C/T]CTATACTTATGAAAA | 405 |
rs776420303 | snp | A/G | 4.97261e-05 | 0.00498604 | missense | ARNT | GRCh38.p7 | 1:150816395 | GTTACAGGAGGGGCT[A/G]GGCCACTATTCCTAG | 405 |
rs776444164 | snp | A/G | 6.61967e-05 | 0.00575273 | intron-variant | ARNT | GRCh38.p7 | 1:150826493 | TAGTCAATATTTATG[A/G]AGTGAATATGACAAA | 405 |
rs776474004 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150848560 | TTTTTCTTTTTTGAG[A/G]CAAGGTCGCCCAGGT | 405 |
rs776510322 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825763 | CTGAAACAGGAGAAT[C/T]GCTTGAACCTAAGAG | 405 |
rs776523588 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150871907 | GTAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 405 |
rs776524291 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | ARNT | GRCh38.p7 | 1:150817311 | AGTACCGGAGAACAC[C/T]TCCTAAGTAAATACT | 405 |
rs776544480 | snp | C/T | 1.72934e-05 | 0.00294048 | intron-variant | ARNT | GRCh38.p7 | 1:150816774 | GTAAAGCAGCACATA[C/T]ATACGGGGCTCACCT | 405 |
rs776575226 | snp | A/G | 1.71146e-05 | 0.00292524 | intron-variant | ARNT | GRCh38.p7 | 1:150813150 | CAGCTTCTAATTTTT[A/G]AAAGTCTTTTCACTC | 405 |
rs776606524 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840645 | TAAAAGTCCCATATG[A/G]GTCCCCAGTCTGGGA | 405 |
rs776646773 | snp | A/C | 0.000182072 | 0.00953955 | missense | ARNT | GRCh38.p7 | 1:150836420 | GAGTCAGACACATAC[A/C]CCACCCTGCCTGTCT | 405 |
rs776656026 | in-del | -/AA | 0.000132477 | 0.00813761 | intron-variant | ARNT | GRCh38.p7 | 1:150814242 | GGGTAGCCACCTGCT[-/AA]AGAGAGATGGAGAGG | 405 |
rs776674161 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150860812 | CAGTGAACCAAGATC[A/G]CACCACTGCACTCCA | 405 |
rs776810112 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150836146 | AAAAAGAACTGACTA[C/T]ATTCATTAAAGTAGA | 405 |
rs776824352 | in-del | -/CACACA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809615 | TCCATCTCTCACACA[-/CACACA]CACACACACACACAC | 405 |
rs776893644 | snp | C/T | 1.65214e-05 | 0.0028741 | intron-variant | ARNT | GRCh38.p7 | 1:150839401 | TTTCAAGAGATTCAC[C/T]CAGATTCCAGACTCT | 405 |
rs776899691 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150855196 | TATGTAACAGCAAAA[C/T]CTTCAAAACAATTTA | 405 |
rs776916936 | snp | A/T | 1.69882e-05 | 0.00291441 | intron-variant | ARNT | GRCh38.p7 | 1:150842501 | GAACTAAGCTAAAAT[A/T]AAAATAAAAAAGAAG | 405 |
rs776921942 | snp | C/T | 0.000127332 | 0.00797807 | missense, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150876565 | GGCAGTAGTCGCCGC[C/T]ATGGCCGCAGATGCC | 405 |
rs776922500 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150869917 | CCAACCAAGCAATGC[C/G]TTGCCCCCAGGCTGC | 405 |
rs776933552 | in-del | -/A | 0.00990075 | 0.0696588 | intron-variant | ARNT | GRCh38.p7 | 1:150853281 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAGTAC | 405 |
rs777004706 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150862981 | GCTTGAACACAAAAG[A/G]CGGAGGTTGCAATGA | 405 |
rs777035487 | snp | C/T | 1.65051e-05 | 0.00287267 | synonymous-codon | ARNT | GRCh38.p7 | 1:150829925 | TCTGCCAATGGCCAC[C/T]AGGCAAAACTTGCTT | 405 |
rs777093546 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821472 | ACAGCATTTTAAGCA[A/T]ACTGGCAACAATTGA | 405 |
rs777161444 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | ARNT | GRCh38.p7 | 1:150817123 | GAAAATCTTGGATCT[C/T]TATCCTGGGCAAATA | 405 |
rs777162532 | snp | C/G/T | 0.0012594 | 0.0250628 | missense | ARNT | GRCh38.p7 | 1:150836387 | TCAGACTGTGGCTGG[C/G/T]TCAAAACAGGAGTCA | 405 |
rs777163535 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859113 | ACATAAATGGGTTTA[C/T]ACATTTCATTCATGC | 405 |
rs777179058 | snp | G/T | 1.73522e-05 | 0.00294547 | intron-variant | ARNT | GRCh38.p7 | 1:150812126 | CTGATAAAAGAAAAA[G/T]ATTAAGTTTGGGTCA | 405 |
rs777273165 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859897 | CTGTAGTCCCAGCTA[C/T]TCAAGAGGTTGATGT | 405 |
rs777285312 | snp | C/T | 1.65168e-05 | 0.00287369 | missense | ARNT | GRCh38.p7 | 1:150823194 | CTGTATAATACATAC[C/T]TCACATTGGTGTTGG | 405 |
rs777343324 | in-del | -/C | 0.0383776 | 0.133101 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876596 | ACCGCCGCCGCGCCA[-/C]CCCCCCCCCCAGTGG | 405 |
rs777348935 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150865599 | CTAACCAAGGCAACT[A/G]CCCCTCTCCATTCTG | 405 |
rs777362763 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150866015 | GAGACAGAGTCTTCG[A/C]TCTTTTGCCCAGGCT | 405 |
rs777368066 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150864328 | AACAGCAACTGTGAA[C/G]AGCTGTAAAGAAAAA | 405 |
rs777374102 | in-del | -/ATTCAC | | | intron-variant | ARNT | GRCh38.p7 | 1:150846688 | AGTAGTGCTAACCAT[-/ATTCAC]ATTGTTGTGCAACAG | 405 |
rs777444553 | in-del | -/T/TT/TTT | | | intron-variant | ARNT | GRCh38.p7 | 1:150840945 | TTATCTCTCTTCTTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 405 |
rs777503128 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150817573 | AACACTTTGGGAGGC[C/T]GAAGCAGGTGGATCA | 405 |
rs777525737 | in-del | -/T | 3.79377e-05 | 0.00435516 | intron-variant | ARNT | GRCh38.p7 | 1:150831942 | AAAAAAAAAAAAAAA[-/T]CTACCCGTAAAACTC | 405 |
rs777556522 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877371 | TCTTTAGGTGCTAAA[A/G]AGCACCTAAACATCA | 405 |
rs777559377 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867620 | TTGGAGTCTTTTATA[C/T]ATAAAAGATAAATAA | 405 |
rs777566539 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150833157 | CAAAGCTAGAATTCA[A/G]ATCCATAGAATATGG | 405 |
rs777592992 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150816517 | TGACTTCCTGCAGGT[C/T]AAGGAAAATTTGATA | 405 |
rs777612583 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866534 | AAGAAATAAAAATGA[C/T]GCCACTGGAGAGAAG | 405 |
rs777621774 | snp | C/T | 1.64857e-05 | 0.00287099 | missense | ARNT | GRCh38.p7 | 1:150817184 | GTTCTGGTCCTGTGG[C/T]TGTCACAGGCTGAAC | 405 |
rs777642281 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150831759 | AAATATTAGCTTTCA[C/T]GGACTCTGTGAGGAA | 405 |
rs777644900 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150863815 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAGTAA | 405 |
rs777671918 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon | ARNT | GRCh38.p7 | 1:150829183 | GATGAACTCTGTTGG[C/T]TGACAAACATTACTC | 405 |
rs777674864 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150871364 | AGAGTGCAGTGGTAC[A/G]ATCTCAGCTCACTGC | 405 |
rs777725321 | snp | A/C | 1.65619e-05 | 0.00287762 | intron-variant | ARNT | GRCh38.p7 | 1:150829854 | AGGAATGAGTCCTGA[A/C]GATCTGCTCTAATTG | 405 |
rs777761656 | snp | C/T | 6.59663e-05 | 0.00574272 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817083 | AGAAAGAAACATACC[C/T]GCATTGATGTTGTGA | 405 |
rs777818784 | snp | C/T | 1.64738e-05 | 0.00286995 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150812011 | ACCCCTTATCCTCAC[C/T]CCAATAGTTCTATTC | 405 |
rs777828195 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845864 | CCGAGATGGCGCCAT[C/T]GCACTCCAGCCTGGG | 405 |
rs777832880 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824031 | TATTTTTAGTATAGA[C/T]GGGGTTTCACCATGT | 405 |
rs777838340 | snp | C/T | 1.67276e-05 | 0.00289197 | intron-variant | ARNT | GRCh38.p7 | 1:150814032 | CAAATCCTTTCTCTT[C/T]AGTGGTGCGATTTTC | 405 |
rs777958186 | snp | G/T | | | missense | ARNT | GRCh38.p7 | 1:150812052 | GGAAACATAGTTAGA[G/T]CAGGGAATTCTTCAT | 405 |
rs777963072 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814126 | GGCAGCAGCACCAGG[C/T]GATGCAGTTGGGGCA | 405 |
rs778047148 | snp | A/G | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810983 | GATTTTCACTGGGAC[A/G]GCTAATCCAAGAAGT | 405 |
rs778047272 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150828307 | TGTAAATTGTATGAG[A/G]TAAGATCTATGTGTT | 405 |
rs778065957 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820741 | TAAGCTGGAAAATGA[A/T]GAACTTCAAACTAAT | 405 |
rs778113427 | snp | G/T | 6.59467e-05 | 0.00574187 | intron-variant | ARNT | GRCh38.p7 | 1:150832444 | AATCAGACTGCCCTA[G/T]CAAAGAACTTTCCAC | 405 |
rs778118594 | snp | A/T | 1.6516e-05 | 0.00287362 | intron-variant | ARNT | GRCh38.p7 | 1:150839681 | GAAAGAGAAGCCCCA[A/T]CCAGGTGGTCACATC | 405 |
rs778132479 | snp | C/T | 1.65228e-05 | 0.00287422 | missense | ARNT | GRCh38.p7 | 1:150852780 | AAAAATTTACTGTTC[C/T]CTTCTCCATCATCAT | 405 |
rs778136998 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150826884 | ACTCCTGACCTCAAG[C/T]GATCCACCCGCCTCG | 405 |
rs778177599 | in-del | -/T | 4.94458e-05 | 0.00497197 | intron-variant | ARNT | GRCh38.p7 | 1:150817314 | CCGGAGAACACTTCC[-/T]TAAGTAAATACTCCC | 405 |
rs778219318 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150837213 | GTTTTCTCAATTCTA[A/G]ATAAATCTTCCCTCA | 405 |
rs778234165 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150867556 | GATATCTTTTAAATA[A/G]ATAAAAATATAGGAA | 405 |
rs778260143 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150824137 | TGAGCCACTGAGCCC[A/G]GCCAGAGACTCAAGC | 405 |
rs778303455 | snp | A/G | 1.65334e-05 | 0.00287514 | intron-variant | ARNT | GRCh38.p7 | 1:150823348 | TTAATTTCACTACCT[A/G]AAAAAGTTTTCATGC | 405 |
rs778303681 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838264 | GCTTCCCAAAATCCA[C/G]AACACTACTCCCCAA | 405 |
rs778304969 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854754 | CCCAGCTACTCGGGA[C/G]GCTGAGGCATGAGAA | 405 |
rs778342133 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150846154 | GAAAGATATTAAACA[C/G]AGAAATTCCGTCTCA | 405 |
rs778352126 | snp | A/C | 2.07084e-05 | 0.00321773 | intron-variant | ARNT | GRCh38.p7 | 1:150836507 | TCCTGCGCAAGAAAA[A/C]GAAATAGAAGTTAAT | 405 |
rs778394054 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150874451 | CCAACTTGGAGAGAC[C/T]GAGGCAAGGCTTGCT | 405 |
rs778405288 | snp | G/T | 1.64754e-05 | 0.00287009 | missense | ARNT | GRCh38.p7 | 1:150839460 | TCAGTGAGGAAAGAC[G/T]GCTTATAGGAGCCAT | 405 |
rs778407215 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820567 | GGGACTGAGGTGGGA[A/G]GATCACTTGAGCCTG | 405 |
rs778422346 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819541 | CGAACATACAGACAG[C/T]ATGTGGTATATCCAT | 405 |
rs778430234 | snp | A/G | 1.67553e-05 | 0.00289437 | missense | ARNT | GRCh38.p7 | 1:150816330 | TGGGGTTGGAGTGGC[A/G]GGAAATCTGGGCCAA | 405 |
rs778451118 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856419 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 405 |
rs778515405 | snp | A/T | | | missense | ARNT | GRCh38.p7 | 1:150817104 | GATGTTGTGATAGAT[A/T]TCTGAAAATCTTGGA | 405 |
rs778530823 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150820936 | AATTCGACTGTAAAC[G/T]TCTGACTCTCCCAAA | 405 |
rs778619170 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838121 | ATTAAAATCTAAATT[C/T]TTTAACACCTAAACA | 405 |
rs778626866 | snp | C/T | 1.65913e-05 | 0.00288017 | missense | ARNT | GRCh38.p7 | 1:150826599 | GACAGAATTCTACAA[C/T]ATTCTTTCCTAAGAG | 405 |
rs778680201 | snp | A/C | 1.76064e-05 | 0.00296697 | intron-variant | ARNT | GRCh38.p7 | 1:150816746 | ATTCAGCAGCTGAAT[A/C]CCTCAGGGCCCTGTA | 405 |
rs778732427 | snp | A/G | | | | | GRCh38.p7 | 1:150830449 | AGAATAAACAAGTAT[A/G]TAAAACTTACCATAT | 405 |
rs778746723 | snp | A/G | 6.31772e-05 | 0.00562002 | | | GRCh38.p7 | 1:150858507 | AAAAAGACAGTCCTT[A/G]CTTATCATCAGTATC | 405 |
rs778751264 | in-del | -/A | | | | | GRCh38.p7 | 1:150855865 | AGCCATGATCATGCC[-/A]CTGCACTCCAGCCTG | 405 |
rs778787249 | in-del | -/CAGA | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877333 | TGAGTGGTTGCCGTG[-/CAGA]CAATGTATCTTGTAA | 405 |
rs778787422 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150848161 | CTGGAAACTGTAGTT[G/T]TCTAAAGAGTTTTGA | 405 |
rs778788216 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809923 | TGAGGGGGGAGGCGT[A/G]CAATGTGATCAGAAC | 405 |
rs778805467 | snp | C/T | 3.51358e-05 | 0.00419126 | intron-variant | ARNT | GRCh38.p7 | 1:150831768 | CTTTCATGGACTCTG[C/T]GAGGAACCAACTGTA | 405 |
rs778820258 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150828665 | CAGTTTTAAAAGTTT[A/G]TATGATGCGTCAATT | 405 |
rs778874610 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150827307 | CTGCCCCAAGATGTT[C/G]CCTTGTGCCATCTGC | 405 |
rs778885896 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150823978 | CTCCCAAGTAGCTGA[A/G]ATTATAGGCACGTGC | 405 |
rs778898922 | snp | A/C | 1.76558e-05 | 0.00297113 | intron-variant | ARNT | GRCh38.p7 | 1:150812140 | AGATTAAGTTTGGGT[A/C]ACACACCTTGATCTC | 405 |
rs778909238 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150816194 | AAACACTGATTTTAC[A/G]TACGGAAAAAAGCCC | 405 |
rs778967904 | snp | C/T | 1.77234e-05 | 0.00297681 | intron-variant | ARNT | GRCh38.p7 | 1:150846237 | TCATATTATATATTA[C/T]AATATATTACCTACT | 405 |
rs778974362 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150838752 | CATGGCTTCCTTACC[C/T]TCAGAAGTCTTCCCT | 405 |
rs778980655 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854750 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCATG | 405 |
rs779071700 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824486 | TTTGAGATGGAGTCT[C/T]GCTCTGTCGCCAGGC | 405 |
rs779105288 | snp | A/G | 3.3305e-05 | 0.00408061 | intron-variant, missense | ARNT | GRCh38.p7 | 1:150842466 | CTCTGCTCATCATCC[A/G]ACCTAAAAATAGAAT | 405 |
rs779111907 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815782 | GGCAGGAGAATGGCG[C/T]GAACCCGGGAGGCAG | 405 |
rs779247367 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861854 | AATGTACAGTGTTCT[A/G]TAAATTACATAATAT | 405 |
rs779249065 | snp | C/T | 3.31044e-05 | 0.0040683 | intron-variant | ARNT | GRCh38.p7 | 1:150829867 | GAAGATCTGCTCTAA[C/T]TGAACGGGAATATAG | 405 |
rs779258068 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854403 | TCTCTACAAAACATA[C/G]AAAAACTAACCAGGC | 405 |
rs779287274 | snp | C/T | 1.91613e-05 | 0.0030952 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150818023 | GCCGTGGTTCTTGGC[C/T]AGAGTTCCTAGGAAA | 405 |
rs779375203 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868624 | CAGCCTGGGCAGGCC[A/G]GGCGCGGTGGCTCAC | 405 |
rs779385419 | snp | A/G | 0.000115587 | 0.00760132 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839600 | ATCTGACAGTTCTGT[A/G]ATGTAGGCTGTCATC | 405 |
rs779429788 | snp | A/G | 1.64985e-05 | 0.0028721 | intron-variant | ARNT | GRCh38.p7 | 1:150834682 | GGAGTGCATTTTTGT[A/G]TGTGGGGAAGAGGGG | 405 |
rs779433337 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870787 | GTGCTAGGATTACAG[G/T]TATGAGCCACCATGT | 405 |
rs779466974 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853001 | AGTACAAAACTGGGG[C/T]CAGGAGTGGTGGCTC | 405 |
rs779486491 | in-del | -/AAAAC | | | intron-variant | ARNT | GRCh38.p7 | 1:150874947 | GTTGCTGTTGTTCAA[-/AAAAC]AAAACAAAATAAAGC | 405 |
rs779512214 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150833581 | ACCTTTAATATCCTA[C/T]CCATAATTTCTAGCA | 405 |
rs779520103 | snp | C/G | 1.6853e-05 | 0.0029028 | intron-variant | ARNT | GRCh38.p7 | 1:150823152 | TTTCTGTTGTGAGAA[C/G]AGAGGAAAAACAGTT | 405 |
rs779541576 | snp | C/T | 1.74741e-05 | 0.0029558 | intron-variant | ARNT | GRCh38.p7 | 1:150816760 | TCCCTCAGGGCCCTG[C/T]AAAGCAGCACATATA | 405 |
rs779585971 | in-del | -/GAT | 1.64861e-05 | 0.00287103 | cds-indel | ARNT | GRCh38.p7 | 1:150813243 | CACTAGAACTTGAAC[-/GAT]GATGAGGCTGCTGGC | 405 |
rs779675517 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150819522 | ACAACCAAATGTCCA[C/T]TAACGAACATACAGA | 405 |
rs779763411 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150836832 | GGGTCACTGAGTCCA[C/G]GAGTTCAAGACCAGC | 405 |
rs779766733 | snp | C/T | 2.78493e-05 | 0.00373147 | intron-variant | ARNT | GRCh38.p7 | 1:150836532 | GTTAATATTTTACTC[C/T]GAAAAAACAAGTATT | 405 |
rs779823347 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872353 | TAAGAATTGTGTTAA[C/T]TGACGCAGTTAAAAC | 405 |
rs779828867 | snp | A/G | 0.000171496 | 0.00925842 | intron-variant | ARNT | GRCh38.p7 | 1:150852890 | TCAACACAAGCTACC[A/G]GAACACCCACCCAAA | 405 |
rs779833641 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828583 | TCTCTTTGTTCTTTG[C/T]TTTCAAGACCTCTTT | 405 |
rs779836626 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150846056 | ACAGAAAAACACTGT[A/G]TAAAATATACCGCCA | 405 |
rs779849599 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835182 | AATTTTAAAAAGAAA[A/G]AAACCAAGTAATTTT | 405 |
rs779851875 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820262 | TCCTGCCAGACTAGA[A/G]CAATAAACTGGTGTA | 405 |
rs779899537 | in-del | -/C | 1.6516e-05 | 0.00287362 | intron-variant | ARNT | GRCh38.p7 | 1:150817227 | CAATGATAAAAATAA[-/C]CCATTAAAGATTTAA | 405 |
rs779908605 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150834048 | CAAGCAATTGTCCTG[A/C]CTCAGCCTCCAAGTG | 405 |
rs779936040 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150823676 | TTGCCTCAGCCTCCC[A/G]AGTGGCTGGGACTAC | 405 |
rs779961431 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150844641 | CAAACTTAATTTTCA[A/G]AAAAGAAATAATTTA | 405 |
rs780013660 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | ARNT | GRCh38.p7 | 1:150839476 | GCTTATAGGAGCCAT[C/G]AGTGGATGTGTTGCC | 405 |
rs780025415 | snp | C/G/T | 3.3046e-05 | 0.00406474 | missense | ARNT | GRCh38.p7 | 1:150813255 | AACGATGATGAGGCT[C/G/T]CTGGCCCTGCCACTG | 405 |
rs780073518 | snp | A/T | 1.70583e-05 | 0.00292042 | intron-variant | ARNT | GRCh38.p7 | 1:150846256 | ATATTACCTACTACA[A/T]TATTACCTGGCAAAC | 405 |
rs780122714 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150824532 | CAATCTTGGCTCACT[A/G]CAACCTCGCCTCCAG | 405 |
rs780124305 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant | ARNT | GRCh38.p7 | 1:150852749 | ATCTAAGGAAAGTTT[C/T]TCAGTCTCTTACCTC | 405 |
rs780131726 | snp | A/G | 1.78363e-05 | 0.00298627 | intron-variant | ARNT | GRCh38.p7 | 1:150831929 | TACAGGAGTTTGAAA[A/G]AAAAAAAAAAAATCT | 405 |
rs780138970 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150841455 | TCTCCACCACATCAT[A/G]CCAAATCCATTTTCT | 405 |
rs780192289 | snp | C/G | 1.7364e-05 | 0.00294647 | intron-variant | ARNT | GRCh38.p7 | 1:150831788 | AACCAACTGTACCAA[C/G]GGGAAATATTTACTA | 405 |
rs780231168 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852613 | ATTAACGGAATGCTT[A/G]AAAATTTTCTGAGAT | 405 |
rs780244819 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868201 | GGTGTACACTTGTAA[A/T]CCCAGCTACTCAGGA | 405 |
rs780285954 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150870103 | TAGATGGACTGCCAA[A/C]AATAAAATTCTGTCT | 405 |
rs780291656 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861510 | CTATCTACAGGTTAA[C/T]GGATAAAGAAACTGT | 405 |
rs780297931 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150832294 | ATGATCTCTGCAGGT[A/G]TTTGGCCATCCCTTT | 405 |
rs780314849 | snp | A/G | 1.65293e-05 | 0.00287479 | intron-variant | ARNT | GRCh38.p7 | 1:150817244 | CATTAAAGATTTAAC[A/G]TGACAATTCAATAAC | 405 |
rs780354320 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810419 | AATATATATGTATAC[C/T]GTAAGTGTGCACATA | 405 |
rs780412296 | snp | C/T | 1.71381e-05 | 0.00292724 | intron-variant | ARNT | GRCh38.p7 | 1:150814290 | CAGCATTAACATCAT[C/T]GCACATACCATGCCT | 405 |
rs780440044 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809788 | CCCTAGTGGTTTTCA[A/C]GTCCCGACTCTTCCC | 405 |
rs780458046 | in-del | -/AAAG | | | intron-variant | ARNT | GRCh38.p7 | 1:150849210 | ATCAGTCTCAAAAAA[-/AAAG]AAAGAAAGAAAATAA | 405 |
rs780469028 | snp | C/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877188 | AATCGCTTGAACCTG[C/G]GAGGCAGAGGTTGCA | 405 |
rs780502733 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150848185 | GTTTTGAAGGTCCAG[G/T]CTGGGGGCAGTGGCC | 405 |
rs780514300 | snp | A/G | 1.9997e-05 | 0.00316198 | intron-variant | ARNT | GRCh38.p7 | 1:150818035 | GGCTAGAGTTCCTAG[A/G]AAACCAGAGTAGACA | 405 |
rs780569270 | snp | A/G | 1.67719e-05 | 0.0028958 | intron-variant | ARNT | GRCh38.p7 | 1:150823165 | AACAGAGGAAAAACA[A/G]TTTTTTCACACTCCT | 405 |
rs780590144 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873064 | CCGAGGCAGGCGGAT[C/G]ACAAGGTCAGGAGAT | 405 |
rs780595204 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868598 | ATCACTCGAGGACAG[C/T]AGTTCAAGACCAGCC | 405 |
rs780601267 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150825261 | AAACAGTATTAGAAG[A/C]TAACCACTTATTTTG | 405 |
rs780629150 | snp | A/G | 9.54699e-05 | 0.00690839 | missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858382 | GCCCTCTGGACAATG[A/G]CTCCTCCACCTTGAA | 405 |
rs780686737 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877339 | GTTGCCGTGCAGACA[A/G]TGTATCTTGTAAATC | 405 |
rs780693893 | snp | C/G | 1.64787e-05 | 0.00287038 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823313 | CCGGAACCGGAACAT[C/G]ACAGACAGCACTTGG | 405 |
rs780710132 | snp | A/G | 4.94833e-05 | 0.00497385 | intron-variant | ARNT | GRCh38.p7 | 1:150817072 | AAAGGATAATGAGAA[A/G]GAAACATACCCGCAT | 405 |
rs780775987 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150847030 | GTCAGTGGACATTTC[A/G]GTTACTTCGACCTCT | 405 |
rs780782146 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150835045 | AGGCAGGAGGACTGC[C/T]TGAGGGCAGGAGTTT | 405 |
rs780784528 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150862040 | TTTATCAAGCCATAA[-/C]CCCCACCATAAGTAC | 405 |
rs780796974 | in-del | -/TTC | | | intron-variant | ARNT | GRCh38.p7 | 1:150813508 | TCAGCCCTAAATTAA[-/TTC]TTCTTCTCCAGGCAG | 405 |
rs780804351 | snp | C/G | 1.65111e-05 | 0.0028732 | missense | ARNT | GRCh38.p7 | 1:150831881 | AGTGAGGTTCCCCAT[C/G]CTTTACAGAGCCAAG | 405 |
rs780831057 | in-del | -/AAA | 0.00108555 | 0.0232722 | intron-variant | ARNT | GRCh38.p7 | 1:150831926 | AGTTACAGGAGTTTG[-/AAA]AAAAAAAAAAAAATC | 405 |
rs780861785 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852494 | ATCCACAGAATTGAG[A/G]AATAACGAACTGTTG | 405 |
rs780902191 | in-del | -/C | | | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876597 | CCGCCGCCGCGCCAC[-/C]CCCCCCCCCAGTGGG | 405 |
rs780920889 | in-del | -/GCTCAACAGATGATTATTTCACCCTTTTTTACCTGGGTGCCA | 3.13102e-05 | 0.00395653 | intron-variant | ARNT | GRCh38.p7 | 1:150817888 | ACCCCCTGGGTGACT[lengthTooLong]GCTGTCCTGAGCCCA | 405 |
rs780963898 | snp | A/C | 1.69263e-05 | 0.0029091 | intron-variant | ARNT | GRCh38.p7 | 1:150836234 | AAGTCTCAGGAAAAA[A/C]ACAAGAAAGGACTTC | 405 |
rs780980513 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150817745 | ACCCAGGAGACAGAG[G/T]TCACAGTGAGCCTAG | 405 |
rs781040150 | snp | C/T | 0.000253068 | 0.0112459 | intron-variant | ARNT | GRCh38.p7 | 1:150829566 | ATGAAAAAATCAAAA[C/T]AATTCCACTTTTCTA | 405 |
rs781041638 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150868497 | AGTATCAAGAACTTG[C/T]AGAGGATTCTAATAA | 405 |
rs781046454 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863844 | AAAGAAGAAGAAAAA[C/G]GCATTCCACATAGAT | 405 |
rs781056802 | snp | A/G | 4.46339e-05 | 0.00472387 | intron-variant | ARNT | GRCh38.p7 | 1:150839665 | TTTCCCTGCATGGAA[A/G]GAAAGAGAAGCCCCA | 405 |
rs781074953 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838543 | ATGTAGTTTTAAGTA[A/G]ACCATCCTATTTGGA | 405 |
rs781127680 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150837779 | GCAGACTTGAATTTC[-/A]AGTATCTGTAAAATA | 405 |
rs781155760 | snp | G/T | 3.29712e-05 | 0.00406011 | missense | ARNT | GRCh38.p7 | 1:150816846 | CCTGGGAGAATAGCT[G/T]TTGGGTGGCAGGGAC | 405 |
rs781261103 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150830295 | AGGATGCAGTGAGCC[A/G]AGATCGCACTACTGC | 405 |
rs781262482 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon | ARNT | GRCh38.p7 | 1:150832399 | AGAGCTACTGCCACA[C/T]CTGTTTCAAGGAATA | 405 |
rs781346501 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150844763 | TTAAACAAATTTAAG[-/T]TTTTTTTCAATCAAA | 405 |
rs781374568 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150831464 | TTCCCCTTTTCTCTC[A/G]AAGTCTTGTTCCTAC | 405 |
rs781389934 | snp | C/G | 2.10099e-05 | 0.00324107 | intron-variant | ARNT | GRCh38.p7 | 1:150817491 | ATTTTTTTTAAAAAA[C/G]AATCTGGAGAAAGAA | 405 |
rs781498297 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824914 | TCGCCCAGGCTGGAG[G/T]GCAGTGGGGCAATCT | 405 |
rs781554419 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150874726 | AGAGGGGACAGGAGA[A/G]AGGGGAGAGGAGAAA | 405 |
rs781571501 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823322 | GAACATGACAGACAG[C/T]ACTTGGCCTTTTAAT | 405 |
rs781589941 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150839725 | GCAGGGAGAGTGATA[C/T]GGATACCAAGTGTGC | 405 |
rs781609336 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150861214 | GAGATGCCTCCAAAA[A/C]TTAAAAATAAAACTG | 405 |
rs781653492 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861804 | GTAGGGCTTTTCACC[G/T]TTATGATAGTGGGAA | 405 |
rs781694598 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | ARNT | GRCh38.p7 | 1:150816314 | GGGGTTGCTCCTTGG[C/G]TGGGGTTGGAGTGGC | 405 |
rs781714426 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867707 | TCCCCAGTGTTGAAG[G/T]TGCAGTCTGGTGGGA | 405 |
rs781715452 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809745 | TTAATCCAGAAAAGG[A/T]CATACTGGGGGAAGG | 405 |
rs781720729 | snp | G/T | 2.98556e-05 | 0.00386354 | intron-variant | ARNT | GRCh38.p7 | 1:150839687 | GAAGCCCCATCCAGG[G/T]GGTCACATCTGGTCA | 405 |
rs781761456 | snp | A/C | 1.72047e-05 | 0.00293293 | intron-variant | ARNT | GRCh38.p7 | 1:150816438 | GAGGTAAAAGATTAA[A/C]AGGATAGATTTATCA | 405 |
rs796157186 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150868490 | ATTATGGAGTATCAA[C/G]AACTTGTAGAGGATT | 405 |
rs796297379 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861407 | ATACCTGAAAGAATT[A/G]AAAGCAGGGTCTCAA | 405 |
rs796312014 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861415 | AAGAATTGAAAGCAG[A/G]GTCTCAAAGAAACAT | 405 |
rs796326142 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150848074 | AACTGAGGAGATAAG[A/T]GTGTGTATGCTCACA | 405 |
rs796344343 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150848468 | CTCAAAAAAAAAAAA[-/A]GGAGTTCTGAAGGTC | 405 |
rs796345125 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150853513 | AAATTTCTGAAACAT[C/T]TTTCAAAGCAGTGAT | 405 |
rs796374961 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150836891 | ACAAACAAACAAAAC[A/G]AAACAAAACAAAAAC | 405 |
rs796390842 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150812272 | TTGACTCCTTTAGAT[C/T]GCAGCCTTTTTTCCT | 405 |
rs796475859 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821828 | TAATTTTTGTATTTT[C/T]TTTTTTTTTTTTTTT | 405 |
rs796477601 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810695 | GGTAAAGGGTGAGGG[C/T]AGTAACCTGTATCCG | 405 |
rs796489826 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150866526 | TCTGTTAAAAGAAAT[-/A]AAAATGATGCCACTG | 405 |
rs796523921 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150839082 | CTAAAACTAGAAGCT[A/G]CTTCAGGGATAAGAA | 405 |
rs796552911 | in-del | AA/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150825858 | CTAAAAAAAAAAAAA[AA/C]CTATATAAAATGAAT | 405 |
rs796567537 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861417 | GAATTGAAAGCAGGG[C/T]CTCAAAGAAACATTT | 405 |
rs796584528 | in-del | -/G | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810762 | TTGAGATGGGTGTCC[-/G]AGGCCCCATCTATCA | 405 |
rs796639160 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150820154 | CAGAGTTGAGTAGGT[A/G]GAATAAAGACCACAT | 405 |
rs796667868 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150874558 | GCGCATGGTGGCAAG[C/G]CACCTGTAGTCCCAG | 405 |
rs796669125 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150852022 | CACTGCACTCCTGGC[A/G]ACAGAGCAAGACTCC | 405 |
rs796670197 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150841316 | AAAAGTTCTTTGTCC[-/A]AAAAAAAAAAGAAAG | 405 |
rs796688370 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810394 | TTTTGGTTTCGTAAA[C/T]TGTGATATAAATATA | 405 |
rs796692497 | in-del | -/TT | | | intron-variant | ARNT | GRCh38.p7 | 1:150828364 | TGTTTTTTTTTTTTT[-/TT]GCATACAGATATCCA | 405 |
rs796700441 | in-del | -/AA | | | intron-variant | ARNT | GRCh38.p7 | 1:150819227 | CTAGATGGCTACAAT[-/AA]AAAAAAAAAGGCAAT | 405 |
rs796712281 | in-del | -/AA | | | intron-variant | ARNT | GRCh38.p7 | 1:150817830 | AAAAAAAAAAAAAAA[-/AA]TTAACCAACCGAACA | 405 |
rs796727864 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150841111 | CACCACCACGCCCAG[-/T]TTTTTTTTTTTTTTA | 405 |
rs796755316 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871298 | AGGCAGTCGTGGTTT[G/T]TTTTTTTTTTTTTTT | 405 |
rs796770547 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150874439 | ACATCTGTATTCCCA[A/C]CTTGGAGAGACTGAG | 405 |
rs796786321 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809650 | AAAAAAAAAAAAAAA[A/C]AAAAAAGTTGCTAAT | 405 |
rs796837180 | in-del | -/TAT | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810721 | TCCGCATTTATATGG[-/TAT]CTATTGTTAATTACC | 405 |
rs796966644 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150819144 | GATCTTCAAGAGGTG[C/G]ATTCAAGGCCAATTC | 405 |