| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs9679 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943285 | TCATTAAAGATAAAA[A/C]ACAGCCAAAGANTCT | 7468 |
| rs14647 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982108 | GCTATTTTCCCCCAA[A/C]TGGCAAGTCTCAACT | 7468 |
| rs373763 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917779 | aaaaaaaaaaaaaaa[A/G]gaaTACTTTTACATT | 7468 |
| rs410630 | snp | A/T | 0.26326 | 0.249648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925774 | AAACAAACaaaaaaa[A/T]atataTATatagata | 7468 |
| rs426891 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931216 | GGACCCCTGTAAGGT[A/G]CAGACTACAGCCGAA | 7468 |
| rs465686 | snp | A/C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933685 | CTTGCAGggccgggc[A/C/G]cggtggcctcacacc | 7468 |
| rs474235 | snp | C/T | 0.431325 | 0.172108 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959410 | CCGAATACCCTTGCA[C/T]ACCCACCACTGCCTC | 7468 |
| rs478530 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972492 | CACTGTCACCCCCAG[A/G]ACACGCCCACCCTTC | 7468 |
| rs479534 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972346 | CTACAACGAGCTTGC[A/G]CTGGGGAAGATTTCC | 7468 |
| rs487903 | snp | A/G | 0.42803 | 0.175514 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900182 | CATAAAAGCAAAATC[A/G]ACACTAACAGGAAAA | 7468 |
| rs489015 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950574 | CCGGGGTGGAGACCA[C/T]GCGTCCTTTCAGAAG | 7468 |
| rs489550 | snp | C/T | 0.00187459 | 0.0305578 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953218 | CTTCAGAGGCAGCCA[C/T]GCTGCTAAAGCACCT | 7468 |
| rs494893 | snp | C/T | 0.224116 | 0.248656 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956444 | TTCTGTAAATTAGTA[C/T]TAAAAATAATTTCTG | 7468 |
| rs495403 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949883 | GACCTTATCAGTGAG[C/T]TTTTCCACATTTAGC | 7468 |
| rs496909 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891791 | cggctcactgcaagc[C/T]ccgcctcccgtgttc | 7468 |
| rs508436 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956260 | ATAAAGATCAAATTT[A/T]AAAAAATAGAAATTA | 7468 |
| rs514882 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936690 | ACTACTCTGTCAGAA[C/T]TTTTTTTTTTTTTTT | 7468 |
| rs515582 | snp | A/C | 0 | 0 | missense | WHSC1 | GRCh38.p7 | 4:1978745 | GGGTGCAGCTGAAGG[A/C]TGTCCCGTCCTGGTG | 7468 |
| rs527355 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919553 | TCTCATGCTTAAAAG[C/G]TTTTTTAGTGTTCAT | 7468 |
| rs527357 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919554 | CTCATGCTTAAAAGC[C/T]TTTTTAGTGTTCATT | 7468 |
| rs528915 | snp | A/C | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906084 | CTGCTTGTGTGCCAC[A/C]CAAACAAATAACATG | 7468 |
| rs530972 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892915 | CCTCAGTAAAAAAAA[A/T]ACAGAGGTTAAACAA | 7468 |
| rs536143 | snp | C/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923418 | TTCTGAAGGAGAAGG[C/G/T]GAAGTCTTTTGGAGA | 7468 |
| rs544270 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906074 | GCCACCCAAACAAAT[A/G]ACATGGGAGTCACAG | 7468 |
| rs546761 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893726 | gaaatcttgtctctg[A/C]aaaaaaatacaaaaa | 7468 |
| rs546903 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942136 | ATTTATCACATATAC[C/T]TTTTCAGAAGATTTA | 7468 |
| rs554570 | snp | A/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906122 | TAAATATCCCCAGAC[A/T]CTAAAAAGGAAATCA | 7468 |
| rs568163 | snp | G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924613 | ACTGAAGGTATACAG[G/T]TAAAACTGAGTTCTG | 7468 |
| rs570175 | snp | G/T | 0.143622 | 0.226238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951444 | GTGTGTGTGTGTGTG[G/T]ATTACATGATGTGTA | 7468 |
| rs573656 | snp | A/G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934847 | ttttttttttttttt[A/G/T]agatggagtctcgct | 7468 |
| rs618034 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924769 | ccgttaattttcttg[G/T]tttgttttgtttttt | 7468 |
| rs632238 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923903 | GTATGTGGCCCTTTT[C/T]AAACTACACAAGTGA | 7468 |
| rs644646 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923426 | TTACTGGCTCTCCAA[A/G]AAACTTGCCCTTCTC | 7468 |
| rs673873 | snp | C/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914906 | CCAACTAAAACAGTC[C/G]TAAGTGTCCCACTGC | 7468 |
| rs673878 | snp | C/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914897 | ACAGTCCTAAGTGTC[C/G]CACTGCAACATCCAC | 7468 |
| rs673887 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914895 | AGTCCTAAGTGTCCC[A/G]CTGCAACATCCACAG | 7468 |
| rs679323 | snp | A/G | 0.095 | 0.19615 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913167 | aggtgaccagaagac[A/G]agagtgtgagccctc | 7468 |
| rs1075781 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969958 | GTGGTTCCTACTCTC[C/T]AGTGTGTTCCTTGAG | 7468 |
| rs1076134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952930 | AGACACTCCCATAAG[G/T]GAGGTGCTGCTGTGG | 7468 |
| rs1076892 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951261 | ACAAATTCGCTCTGC[A/C/G]TACCGGGGCCCCAGT | 7468 |
| rs1079730 | snp | C/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886031 | TTTTGGTTGGTGAGA[C/G]CAGAGTTGTATGTAT | 7468 |
| rs1132849 | snp | G/T | 0.0562649 | 0.15989 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979529 | GTGGCAGCAATGGTG[G/T]TGTAAGATTTCCTCC | 7468 |
| rs1132852 | snp | A/C | 0 | 0 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979789 | TGCTAAACCTATTTC[A/C]CAAATCACCACCGAC | 7468 |
| rs1132853 | snp | G/T | 0 | 0 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981392 | GCCCTGCCCAGCTTT[G/T]TTCTGAGGACGTGGT | 7468 |
| rs1133476 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942186 | AATTATTACATGGTA[A/C]TACATCACCCTGAGG | 7468 |
| rs1980626 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937797 | ACTGTCCTGTCCCCA[A/C/T]AGCACTAGAGCAGCG | 7468 |
| rs2180857 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938179 | CCGCTCTCGCATCTG[A/T]CAGGAGGGCGAGGTG | 7468 |
| rs2187692 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981829 | CATCAACTACACTCA[C/T]AGGATCAAGATATTT | 7468 |
| rs2236997 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922773 | tctactaaaaatata[A/G]aaattagttgggcat | 7468 |
| rs2754197 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894899 | ttcagtttgagaaga[G/T]gaaaaagttctggag | 7468 |
| rs2759718 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893534 | aaaaaacaaaAAAAA[A/C]AAAAAGAGGCAAAAT | 7468 |
| rs3135122 | snp | A/G | 0.432357 | 0.171014 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961370 | ACCCGGACAAGCAGA[A/G]CCTCAGGGTGCCTGG | 7468 |
| rs3135148 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934875 | tatatatatatatat[A/T]ttttttttttttttt | 7468 |
| rs3197006 | snp | A/G | 0.0204249 | 0.0989712 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942537 | AACACATACAATGAA[A/G]AAAACAGATAACAAA | 7468 |
| rs3216203 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910244 | CAACCtttttttttt[-/T]cgagacagtctttct | 7468 |
| rs3216204 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935881 | aaaacaaacaaaaaa[-/A]CCCCCAAACACCATA | 7468 |
| rs3762937 | snp | A/C | 0.0685596 | 0.171987 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891862 | ACTCCATCTCAAAAA[A/C]AAAAAAAAACAAAAA | 7468 |
| rs3792716 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933629 | TCGATCTCCTGACCT[C/T]GTGATCCACCCACCT | 7468 |
| rs4299658 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920861 | caacatgaaaccctg[C/T]ctctaaaaaaaaaaa | 7468 |
| rs4318713 | snp | C/T | 0.231482 | 0.249313 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879375 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 7468 |
| rs4865478 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914227 | gagaccagcctggcc[A/G]acatagcaaaacccc | 7468 |
| rs4865481 | snp | G/T | 0.499609 | 0.0139722 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872637 | TCACAGGGTCTGCGC[G/T]CTCTCTCTCTCTCTC | 7468 |
| rs5855722 | in-del | -/AA | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873799 | ACCATCTTAGCACTT[-/AA]CTTTTAAGTTCTTGC | 7468 |
| rs6599402 | snp | A/G | 0.232359 | 0.249377 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886388 | atttttgtattttta[A/G]tagagacagggtttc | 7468 |
| rs6814150 | snp | G/T | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915984 | GGTACCTCCTTTCTT[G/T]TATTTTGGGCCCGTC | 7468 |
| rs6814151 | snp | G/T | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915985 | GTACCTCCTTTCTTT[G/T]ATTTTGGGCCCGTCT | 7468 |
| rs6814391 | snp | C/T | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916135 | TGATGCTCCTGTCAC[C/T]CTAGCACTGTGAGAT | 7468 |
| rs6820307 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946775 | ATCTGATTCCTATAC[C/T]GGATGAGCAAGGAGC | 7468 |
| rs6822607 | snp | G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882212 | TGATTGGATTGGACA[G/T]CCCTGTCTCCTTGAA | 7468 |
| rs6830342 | snp | C/G | 0.239902 | 0.249796 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870404 | GCTCCCTGAACCTGC[C/G]TGACAGAAAACCCAA | 7468 |
| rs6853594 | snp | G/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893556 | ttgtttttttttttt[G/T]tttgttttgttttga | 7468 |
| rs7377981 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958873 | AAGAGTGTCTTTCGC[C/T]ACCTCTTCCCTAAGA | 7468 |
| rs7441707 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934878 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 7468 |
| rs7657447 | snp | G/T | 0.185155 | 0.241444 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921215 | gtaatcccagcactt[G/T]gggaggctgaggcgg | 7468 |
| rs7669316 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931135 | TGATGTGGTAGGGTC[A/G]GCCTTCAGGCCTGTG | 7468 |
| rs7673596 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872591 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 7468 |
| rs9631824 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874080 | ACCTTTCTAAGTAAA[C/T]AATTAATCAGCAGCA | 7468 |
| rs9799374 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878286 | ttttttttttttttg[G/T]atttttagtagagac | 7468 |
| rs9993250 | snp | C/T | 0.119281 | 0.213102 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881269 | gttttgtttttgttt[C/T]tgtttttttgagacg | 7468 |
| rs9996424 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920206 | tgtaatctcagcaca[C/T]tgggaggctaaggtg | 7468 |
| rs9997044 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882872 | gtggggcccaacaat[A/C]tgtgttctaatgtgt | 7468 |
| rs9999240 | snp | C/T | 0.115438 | 0.210697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923684 | aaattgaagatgtgc[C/T]tttttttctcttaca | 7468 |
| rs9999420 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923839 | CAATTAAAGTGAACT[A/C]ATTGGATGTCAAAGC | 7468 |
| rs9999954 | snp | A/G | 0.188 | 0.24219 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891901 | CAAAAACGAAAAAAC[A/G]AAAAACCTCACCAGA | 7468 |
| rs10000617 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881361 | tccgcctcctgggtt[C/T]acgccattctcctgc | 7468 |
| rs10002574 | snp | C/T | 0.124837 | 0.216412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922023 | cgtggtgatgcgcgc[C/T]tgtaatcccagctac | 7468 |
| rs10004765 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930849 | CTCTGATCTTGGAAC[C/T]GTAGGGAAGTGTGTC | 7468 |
| rs10005999 | snp | G/T | 0.0114282 | 0.0747228 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893543 | CTTTTTTTGTTTttt[G/T]ttttttttttttttt | 7468 |
| rs10006069 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959930 | cagtggcatgattgt[A/C]gttcactgcagcctc | 7468 |
| rs10008627 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891688 | aaaccccatctctat[C/G]aaaaatacaaaaata | 7468 |
| rs10009780 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924811 | GCACACTTGTAGTCT[C/T]AGTTACTCAGGAAGC | 7468 |
| rs10013545 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908855 | cacaatcatagctca[C/G]tccaggctcaaactc | 7468 |
| rs10019114 | snp | A/G | 0.119281 | 0.213102 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893337 | gagccaggcgtggtg[A/G]tgcatgcctgtagtc | 7468 |
| rs10019502 | snp | A/G | 0.119281 | 0.213102 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893735 | ttttttgcagagaca[A/G]gatttcgccatgttg | 7468 |
| rs10021693 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903934 | agagacagggtttca[C/T]tgtgttagccaggat | 7468 |
| rs10023086 | snp | C/T | 0.126219 | 0.217206 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909096 | GTTATATATTTTAGT[C/T]Cttattttcttaaat | 7468 |
| rs10024338 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934523 | agataaaaTACTGGG[G/T]tatatttaaatttaa | 7468 |
| rs10026943 | snp | G/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910783 | CATGGGATTGTGGAT[G/T]TGCTGTTTTTCTACT | 7468 |
| rs10027958 | snp | C/G | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926790 | TTTTAATTTTTAAAG[C/G]CTTTTCTACCTTTCC | 7468 |
| rs10029255 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977797 | actccactcaaaaaa[A/G]aaaaaaaccaaacaa | 7468 |
| rs10034373 | snp | C/T | 0.0759472 | 0.179459 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980928 | GTTCTAGGGACAGGC[C/T]GGGCAGTGTCCCCAC | 7468 |
| rs10488835 | snp | G/T | 0.105569 | 0.204058 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945597 | GAGTGTGTGGCACCT[G/T]TGATGGCAGGGCTGT | 7468 |
| rs11248080 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878710 | AGGGGAGTGGTGTGA[A/G]CATTTTGCCTTGATG | 7468 |
| rs11248081 | snp | A/G | 0.124491 | 0.216211 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889628 | TTCCTCAGCCTCCCA[A/G]GTAACTGGGATTACA | 7468 |
| rs11545893 | snp | A/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980901 | CCTTATGATGCCCTA[A/T]CTTGGAAGGTTGTTC | 7468 |
| rs11721754 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926226 | gaggcatgatctcgg[C/G]tcactgcaacctccg | 7468 |
| rs11726032 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887565 | actgtagcctccaac[C/T]cctgggctcaagcag | 7468 |
| rs11726452 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938601 | GGGTGGGTGGGCTGA[A/G]AGTGTGAAAGGGGAA | 7468 |
| rs11729388 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916033 | CCTGGCTGCACTGTG[A/G]GACGTGGCTTCTTCC | 7468 |
| rs11731257 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934718 | ctgggcgtggtggca[C/G]gtgcctgtaatccca | 7468 |
| rs11733932 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934880 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 7468 |
| rs11930769 | snp | A/G | 0.125528 | 0.21681 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925556 | ggcacatgccaccac[A/G]tccggctaatttttg | 7468 |
| rs11930983 | snp | C/G/T | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881646 | aagcagtccttctgc[C/G/T]tgcacctcccaaagt | 7468 |
| rs11933988 | snp | C/T | 0.187053 | 0.241946 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881562 | gccaccgtgcctggc[C/T]tgtttttgtttttaa | 7468 |
| rs11937262 | snp | A/G | 0.132066 | 0.220435 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960807 | AGCAAGGGTTGGCAT[A/G]TTGCCACTTCGTGAA | 7468 |
| rs11937964 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875802 | tagtcccagctactc[G/T]ggaggctgaggcagg | 7468 |
| rs11943579 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925560 | catgccaccacatcc[A/G]gctaatttttgtatt | 7468 |
| rs11945131 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981400 | CAGCTTTGTTCTGAG[A/G]ACGTGGTGACTTCCT | 7468 |
| rs12648105 | snp | A/G | 0 | 0 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979123 | TCTGAGCCCAGCTCA[A/G]CGTTCCTGGACAAAC | 7468 |
| rs12651035 | snp | A/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877374 | GACTCTCACTGCCCA[A/T]TGGGGTTCAAGACGA | 7468 |
| rs13111999 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927618 | cagctactcaggagg[C/G]taaggtgggagaatc | 7468 |
| rs13112026 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927666 | agaggttgcagtgag[C/T]tgagatcacgtcact | 7468 |
| rs13112033 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927675 | agtgagctgagatca[C/G]gtcactgcactccag | 7468 |
| rs13112062 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927710 | ggccacaatgagact[C/T]ttatctcagaaaaaa | 7468 |
| rs13114773 | snp | C/T | 0.109461 | 0.206758 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892365 | GAGTCCCTCCCCTCA[C/T]GTTGGAGACCTCCCA | 7468 |
| rs13117796 | snp | A/G | 0.283684 | 0.24772 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878508 | CCATGTGAATTCCTG[A/G]CTGCATTGGGTCATC | 7468 |
| rs13119410 | snp | A/C | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870943 | CTCACGGGACAGGAG[A/C]TTGGGGAcccgcgcg | 7468 |
| rs13119446 | snp | C/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870984 | gcgcccaacgccagc[C/T]tccgcggccgcgcgc | 7468 |
| rs13122254 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927639 | tgggagaatcgcttg[A/T]acccaggaggcagag | 7468 |
| rs13122255 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927640 | gggagaatcgcttga[A/C]cccaggaggcagagg | 7468 |
| rs13122284 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927684 | agatcacgtcactgc[A/C]ctccagcctgggcca | 7468 |
| rs13122295 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927699 | actccagcctgggcc[A/C]caatgagactcttat | 7468 |
| rs13143179 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927652 | tgaacccaggaggca[C/G]aggttgcagtgagct | 7468 |
| rs13148597 | snp | C/T | 0.204496 | 0.245824 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902627 | TGTTTTGTTTTGAGA[C/T]AGGGTCTTGGTATGT | 7468 |
| rs13435616 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880705 | gagaaatactacaga[C/G]ttgccattggcaaca | 7468 |
| rs13435794 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872629 | gagagagagagagag[A/C]gagagagCGCGCAGA | 7468 |
| rs17132074 | snp | C/T | 0.130351 | 0.219509 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878973 | GGTAGTTGCTGGTAC[C/T]GTTACCTCTCTGTGA | 7468 |
| rs17132079 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902112 | CTTTTTAGTTGTAAC[G/T]CCTTGAAATTGTTAA | 7468 |
| rs17132080 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905354 | ATCTGATCTGTGCAC[C/T]CTCTGGAAGTGTGGC | 7468 |
| rs17132081 | snp | G/T | 0.125528 | 0.21681 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906987 | TCTTTGCTTGACTCC[G/T]GGACCTTGCACTGTG | 7468 |
| rs17132088 | snp | A/G | 0.0387552 | 0.1337 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941444 | TGAGGCCAGTGTAGC[A/G]GGGTCGAGGCCTGCC | 7468 |
| rs17132090 | snp | C/T | 0.144296 | 0.226554 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949235 | TGTGCGCTGTGGCTC[C/T]TGCAGGGCCCTCCTG | 7468 |
| rs17132092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952960 | TGTCTGCCTGCCCAG[A/G]ATGATAAGTGACTGC | 7468 |
| rs17132093 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956747 | ATGATCGGTCAAGAG[A/C]GAATGAGGCCAGTAG | 7468 |
| rs17132099 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960908 | GAGACTTTGTACACG[C/T]CCTCCACGGAGGTAT | 7468 |
| rs17132100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961329 | TCAGCTGCGCCGGAG[A/G]GCTAGAGCTAACCAC | 7468 |
| rs17132105 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968154 | GGAGAGAGCTGACCA[C/T]CAGTATAATTTAGCT | 7468 |
| rs17132108 | snp | C/G | 0.145978 | 0.227331 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978233 | AGGGTGGTCCCTAAC[C/G]TGACAGAGCTTTTAC | 7468 |
| rs17746800 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893054 | TACAACAGCACTTCT[C/G]CAGTACCAATCTGAT | 7468 |
| rs17803236 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874653 | GGCTTGGCTAAGGTC[A/G]CTCTGAAACATTGCA | 7468 |
| rs17803703 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927390 | ACCTAAACATTCTTC[A/G]CTGAATCCTGAAAGC | 7468 |
| rs28361409 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885129 | AAAAAAAAATAAAAA[A/T]AAAAAAAATAAAATT | 7468 |
| rs28362025 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933544 | ACAGGCGCCCGCCAC[C/T]ATGACCAGCTAATTT | 7468 |
| rs28370433 | snp | A/G | 0.116138 | 0.211142 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877885 | TACTCTGTTGTGACC[A/G]GGTACTATTACAGTT | 7468 |
| rs28372055 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884979 | GCCAGGCGTGGTGGC[A/G]GCAACCTGTAATCTC | 7468 |
| rs28415064 | snp | C/T | 0.191147 | 0.242974 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977051 | AGGCCTCTACAACAG[C/T]GTCTCCCTGGCAGCC | 7468 |
| rs28438603 | snp | A/C/G | 0.044663 | 0.143489 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882553 | CCTGTAGTCCCAGCT[A/C/G]CTCGGGAGGCTGAGG | 7468 |
| rs28461181 | snp | A/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878253 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 7468 |
| rs28463244 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967433 | AAATACAAAAATTAG[C/T]TGGGCGTGGTGGCGG | 7468 |
| rs28469487 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884833 | AACTGCCTGGGCTGG[A/G]CGTGGTGGCTCACGC | 7468 |
| rs28478478 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875729 | AACATGATGAAACCC[A/C]GTTTCTACTAAAAAA | 7468 |
| rs28516674 | snp | A/G | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911518 | GCTTGAGCCCAGGAG[A/G]CAGAGGTTGCAGTGA | 7468 |
| rs28530624 | snp | C/T | 0.185155 | 0.241444 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937373 | TACCTTCTATTAAAG[C/T]AGCCCTTTGCTGGCA | 7468 |
| rs28541559 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967723 | GACACAGTCAGTGTT[G/T]CCAGAGAAGAAAGGC | 7468 |
| rs28577009 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936925 | ACAGAACATTCTTCT[A/G]GGGCACCTGCCATAG | 7468 |
| rs28594940 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882076 | TGGAAAGAAGATTCC[C/T]CAGATTGCTCTGTAG | 7468 |
| rs28620559 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913952 | AAGTTTTCTTTTTTC[C/T]TGGAGGCTATTTTTG | 7468 |
| rs28644405 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959008 | TATGCCCTCCTGCCT[A/G]GCACTGCTCCTCCTG | 7468 |
| rs28649542 | snp | A/G/T | 0.00795939 | 0.0626292 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977183 | CCAGGAGGCTCCGCC[A/G/T]GTTGACGAAGGAGCT | 7468 |
| rs28662327 | snp | C/G | 0.124491 | 0.216211 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972933 | TCTCAGCTCACTGCA[C/G]CCTCTGCCTCACAGG | 7468 |
| rs28671538 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895748 | AGGTTTCCCTGCAGG[C/T]CCTACCAGTGTCACT | 7468 |
| rs28673461 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968614 | GGAAGGAGAAATAAT[A/C]GTAATTAGAAAGCAC | 7468 |
| rs28673589 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961514 | TTTAATTTTCAGTGC[C/T]CTTTGGGTAAGGTCT | 7468 |
| rs28693988 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878168 | TGGGTTCAAGCGGTT[C/T]TCCTGCCTCAGCCTC | 7468 |
| rs28694216 | snp | C/T | 0.124837 | 0.216412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933743 | AACCCTGAACCCCTC[C/T]GTAAAGCAGTCATGC | 7468 |
| rs28707257 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934086 | AAAGATTTTTTTTTT[G/T]TTTTTCGTTTTTTTT | 7468 |
| rs28731134 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934882 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 7468 |
| rs34000332 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917798 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTGC | 7468 |
| rs34004938 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877723 | CCTGCTCTGAAGCCC[-/TG]CAGCTCTGCTGCCTC | 7468 |
| rs34059441 | in-del | -/A | 0.0678174 | 0.1712 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885124 | TCAAAAAAAAAAAAT[-/A]AAAATAAAAAAAATA | 7468 |
| rs34096276 | in-del | -/A | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934856 | AAAAAAAAAAAAAAA[-/A]TATATATATATATAT | 7468 |
| rs34154038 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877693 | TCATTCTGTTCCAGC[-/C]ACACGGGCCTCTTGC | 7468 |
| rs34168382 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880771 | TACTCATCAACAGGG[-/G]AAAAATGAAGGGGAC | 7468 |
| rs34192394 | in-del | -/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907471 | TACTTGGATTCTAGC[-/T]TTTTTTGTGTATGTG | 7468 |
| rs34231356 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885206 | CACTATCTACCTTTT[-/T]AGGCTGAATGCATGT | 7468 |
| rs34236505 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901624 | CCAAGGTGTTCTTTA[-/G]CCTGATGTGGTCAGT | 7468 |
| rs34242285 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875229 | TCCCAAAGTACTGGG[-/G]ATTACAAGTGTGAAC | 7468 |
| rs34251816 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895160 | CTGTGCAGATAGTCT[A/G]CATTTTGGTTATCTA | 7468 |
| rs34309638 | multinucleotide-polymorphism | GC/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877727 | CTCTGAAGCCCTGCA[GC/TG]TCTGCTGCCTCCGAC | 7468 |
| rs34314028 | in-del | -/C | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1954678 | TGGTTTTAATGGCCC[-/C]ATTATATGTAAGAAA | 7468 |
| rs34335852 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925390 | TTTTCTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 7468 |
| rs34376127 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877372 | GTGACTCTCACTGCC[-/C]ATTGGGGTTCAAGAC | 7468 |
| rs34391918 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901853 | CCCAGTGCAGAGCCC[-/C]AGCACACTGAACACA | 7468 |
| rs34480893 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971502 | AGAATACACTGGAGG[-/G]AAGTGTTTAGAGACC | 7468 |
| rs34587750 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968380 | CTAATGGTCACAGGG[-/G]AGCACCGGGAGCGTG | 7468 |
| rs34601712 | in-del | -/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925416 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 7468 |
| rs34632149 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932715 | GTGCCATTGGATTCC[-/C]AGCCAATGGAATGGC | 7468 |
| rs34667949 | in-del | -/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946015 | AGCCCTTTTGCCTTA[-/G]TGTGAAAATGTAACA | 7468 |
| rs34674931 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876576 | TGTGCCTATAGTCCC[-/C]AGATACTTGGGTGGC | 7468 |
| rs34685080 | in-del | -/A | 0.305685 | 0.24372 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897175 | ACTCTGTCTCAAAGG[-/A]AAAAAAAAAAAGGAA | 7468 |
| rs34717201 | in-del | -/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942933 | GATTCTATCCTTTTT[-/T]ACTAAACAGTTTTAT | 7468 |
| rs34772768 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923338 | AAAAAAAAAAAAAAA[-/A]TTCTTATGTGTCAAG | 7468 |
| rs34883176 | in-del | -/C | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981477 | AAACCGCCCCAATCC[-/C]TCAGGATTCCTTGGC | 7468 |
| rs34890746 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907638 | TTTTTTTTTTTTTTT[-/T]GTGACACAGTCTCAC | 7468 |
| rs34891175 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912570 | CCTTAAAACTCATCC[-/C]TTATTATGAAGTTAG | 7468 |
| rs34909350 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932068 | TTTAATCCTGACTTT[-/T]CAGGTGACCCTGGTG | 7468 |
| rs34910181 | in-del | -/A | | | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1916880 | ACTAGGTCAGAAAAA[-/A]GAGTGCACGCCAGTA | 7468 |
| rs34948395 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916659 | TTGGCTTTCTTTCCC[-/C]ATTCAATTTTGAACC | 7468 |
| rs34960531 | in-del | -/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951012 | GAGCCTGCCTGCAGG[-/G]CATGGCCACCCGCTG | 7468 |
| rs34976980 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929028 | GTGCTGGGGGTCAGA[-/A]GCCAGACCCAGAACT | 7468 |
| rs35007906 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872589 | GTGTGTGTGTGTGTG[A/T]GTGAGAGAGAGAGAG | 7468 |
| rs35068351 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874275 | GTAGTAAGTGTGACC[-/C]TTGTTCTCCAAATAC | 7468 |
| rs35093726 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927010 | TGGTTCTGCCTTAGG[-/G]TCTCTTGAAGTTGCA | 7468 |
| rs35109774 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944760 | TATCTGCTTCTAAAA[-/A]TTGCCCCACCTGCTC | 7468 |
| rs35119483 | in-del | -/AT | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903219 | TGGAACAATTTACTC[-/AT]GTGTATAGTGCTCTT | 7468 |
| rs35142760 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922271 | AGTTCACCAGGATAT[-/T]AAAATTAACATACAA | 7468 |
| rs35224531 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892583 | AACTCTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 7468 |
| rs35239560 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892661 | TGTAACCTCCGCCTC[-/TC]GGGTTTGAGCGATTC | 7468 |
| rs35256815 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969558 | AAAAAAAAAAAAAAA[-/A]TAGCTGGGCACAGTG | 7468 |
| rs35258624 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889267 | AGTGGTGTAATTATG[-/G]CTCACAGCCTCTACC | 7468 |
| rs35322066 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872587 | GTGTGTGTGTGTGTG[A/T]GTGTGAGAGAGAGAG | 7468 |
| rs35400064 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907145 | AAGCTTCAGTTTCCC[-/C]TGTATATGAAAATGA | 7468 |
| rs35402766 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936183 | TGGTACCTGCAGGGG[-/G]AGTGAAACCAACCAA | 7468 |
| rs35410897 | in-del | -/CC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958589 | GCAAGCCGCATCCCC[-/CC]AGGAGCCTCGTGGCC | 7468 |
| rs35411136 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944142 | GCAGGGGCAAGTGAA[-/A]CTCAGCACTCTGCAG | 7468 |
| rs35417292 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978462 | GGAGTCAACAGGCCC[-/C]TGCCAGGGAGCCCGC | 7468 |
| rs35427928 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911482 | ATCCCAGCTCCTGGG[-/G]AAGGCTGAGGCATGA | 7468 |
| rs35431239 | in-del | -/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982066 | TTGAAATTCACTTTT[-/T]GGGGGGAGGGATATA | 7468 |
| rs35439740 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897093 | GAAGATCACTTGAGC[-/C]TGGGAGGCAGAGGTT | 7468 |
| rs35448464 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926173 | TTTTTTTTTTTTTTT[-/T]AAGACGTAGTCTCGC | 7468 |
| rs35460241 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936200 | TGAAACCAACCAAGG[-/G]AAACACCGGGTTATT | 7468 |
| rs35519246 | in-del | -/A | | | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1978830 | CACCAAGACTGAGAA[-/A]GCCCCCCCCAGAGCC | 7468 |
| rs35561111 | in-del | -/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873800 | CAAGAACTTAAAAGA[-/TT]AGTGCTAAGATGGTG | 7468 |
| rs35593692 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877873 | ACTGATTTAAAGTAC[G/T]CTGTTGTGACCAGGT | 7468 |
| rs35623015 | in-del | -/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932009 | GTGACAGTTGAGTTT[-/T]CTGCCCACAGTGTGT | 7468 |
| rs35648360 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968066 | AGCATATTAAAAGAA[-/A]TTACACACCAGGGAA | 7468 |
| rs35712034 | in-del | -/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943907 | CCAGCCAGCTAGCCC[-/C]ATAACTGATAGATGC | 7468 |
| rs35838443 | in-del | -/G | | | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1978639 | TGTTCTGTTGCAGGG[-/G]AAGTGGGAATGTCCT | 7468 |
| rs36005375 | in-del | -/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953579 | CAGGCCAGACGCAGG[-/G]CCCATGGGCGCTTGG | 7468 |
| rs36021467 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892981 | TCATGTTGCATTTGT[A/G]ATTTTAAGAAGAAAA | 7468 |
| rs36052132 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877375 | ACTCTCACTGCCCAT[-/T]GGGGTTCAAGACGAG | 7468 |
| rs36080711 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916633 | GGCGTGAGGGACTGC[-/A]GCCTGGCCTGGTTGG | 7468 |
| rs36113548 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895680 | GTGTTTACCTCAGGG[-/G]CATCTCTCAGTGGCT | 7468 |
| rs36222330 | in-del | -/TGTCT | 0.124837 | 0.216412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937554 | GAAGTAATGGTGTCT[-/TGTCT]CTTCAGATTTGGGTT | 7468 |
| rs55669110 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887913 | AGTTCCTTTTTTTCT[G/T]TTTTTTTTCTTCTGT | 7468 |
| rs55720454 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920484 | AAGCTATTATTGTGA[C/T]TTACTGTGTA | 7468 |
| rs55739348 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882534 | CTGGGCGTGGTGGCG[A/G]GCGCCTGTAGTCCCA | 7468 |
| rs55742969 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920605 | TTTGGTACGTGCATT[A/G]AAGTTCATTGCTTTT | 7468 |
| rs55778318 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882402 | GGGCTTAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7468 |
| rs55783621 | snp | A/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954185 | AGACGGGGTTTCATC[A/T]TGTTGGTCAGGCTGG | 7468 |
| rs55964764 | snp | A/G | 0.186105 | 0.241697 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973902 | AGGCCGGGGCCGTCC[A/G]TTCCCTGCTGCTGGG | 7468 |
| rs56072223 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920058 | GGCAGAGATGCATAA[A/G]TGGGTGACTGTGAGT | 7468 |
| rs56165638 | snp | C/T | 0.135825 | 0.222405 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887921 | TTTTTCTTTTTTTTT[C/T]CTTCTGTGATGACCT | 7468 |
| rs56205946 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909614 | AGCCAGTACTTTTAT[A/G]TTTTTCTATCCTCTA | 7468 |
| rs56302455 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967766 | GACATCAGACGAGAC[C/T]AGCCTCAAATCCATC | 7468 |
| rs56372494 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965052 | GTCCAGTGTTCAGCA[-/A]AAAAAAAAAAAAAAA | 7468 |
| rs57130786 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878145 | GGCTCACCACAACCT[C/T]TGCTTCCTGGGTTCA | 7468 |
| rs57235054 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896843 | TTCTTCTCTTCTCTT[C/T]TCTTTTCTTTCTCCT | 7468 |
| rs57276793 | snp | A/G | 0.00421722 | 0.0457255 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956205 | TACGGAGATATTCAG[A/G]TAGAGAGTGAGACAG | 7468 |
| rs57356953 | in-del | -/TATTCGAAGTG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966048 | GGCAGTGGGCCAATG[-/TATTCGAAGTG]CTAAAAGAAGAAAAA | 7468 |
| rs57548242 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924759 | CTACAAAAAAAAAAA[-/A]CAAAACAAAACAAGA | 7468 |
| rs57661770 | snp | C/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876799 | AATTTTTAAGTTGAC[C/G/T]TGAGTTGGCACTGAG | 7468 |
| rs57703773 | in-del | -/CGTACATT | 0.0998734 | 0.199905 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966371 | GCATGATTGAAGAGA[-/CGTACATT]TAGGGCTGGGCATGG | 7468 |
| rs57783080 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897230 | CTCATGCCTGTAATC[C/T]CAGTACTTTGGGATG | 7468 |
| rs57804419 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957467 | TTTTTTTTTTTTTTT[-/T]GTAGAGAATGGGGTT | 7468 |
| rs58007182 | snp | A/T | 0.0865458 | 0.189163 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873827 | GGTGCTGAAGTTCAT[A/T]ATCCAAACGTATTTT | 7468 |
| rs58010570 | snp | A/G | 0.0220997 | 0.102769 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930576 | GCAAAACAAAACCCA[A/G]TGAGTTTTACGGATT | 7468 |
| rs58015003 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922700 | GGAGGTCAAGGCAGG[C/T]GGATCACCGGAGGTC | 7468 |
| rs58054517 | snp | C/T | 0.124837 | 0.216412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902108 | GTTGCTTTTTAGTTG[C/T]AACTCCTTGAAATTG | 7468 |
| rs58262875 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974038 | ATCAGGTTGCTGCCT[C/T]GAAAGCCTTCCTGCC | 7468 |
| rs58339564 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951456 | AATACACACACACAC[-/A]CACACACACACACAC | 7468 |
| rs58548271 | snp | G/T | 0.0667028 | 0.170006 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885628 | TGCTGGAGTGTGGAG[G/T]CATGCTCTGGGTCCT | 7468 |
| rs58817114 | in-del | -/AA/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934909 | ATATATATATATATA[-/AA/T]AAAAACAGATAAAAC | 7468 |
| rs59068985 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925534 | CTCCCGAGTTGCTGA[A/G]ACCACAGGCACATGC | 7468 |
| rs59176209 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970120 | GAGGCACTGTGCATT[C/G]AAGCAGGCCAGAGGA | 7468 |
| rs59360543 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876763 | AAATGCTTTTTTTTT[-/T]CTGGAAGGAATTGGA | 7468 |
| rs59619163 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934876 | AAAAAAAAAAAAAAA[-/T]AAATATATATATATA | 7468 |
| rs59717604 | snp | C/T | 0.124144 | 0.21601 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966404 | GCTCACGCCTGTAAT[C/T]CCAGCGCTTTGGGAG | 7468 |
| rs59927319 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895255 | GTACAAATATCTTCT[C/G]GTTCCTGCTTTTAAT | 7468 |
| rs59927644 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934910 | TATATATATATATAA[-/T]AAAACAGATAAAACA | 7468 |
| rs60480173 | snp | C/T | 0.0201127 | 0.0982437 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953289 | TTCTTGTTCTTTGCA[C/T]CTCTCTCTCCACCCC | 7468 |
| rs60574846 | snp | G/T | 0.0766824 | 0.180169 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873618 | TGGGGCTTACATGGG[G/T]ACAGCCTTCTGCCTA | 7468 |
| rs60912477 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934877 | AAAAAAAAAAAAAAA[-/T]AATATATATATATAT | 7468 |
| rs61229354 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928310 | ATCTAGTACTCCTCA[A/G]AATCACCTTATAAGG | 7468 |
| rs61238782 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887921 | TTTTTCTTTTTTTTT[-/T]CTTCTGTGATGACCT | 7468 |
| rs61324794 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923338 | AAAAAAAAAAAAAAA[-/A]TTCTTATGTGTCAAG | 7468 |
| rs61397233 | in-del | -/AAAAAA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888432 | AAAAAAAAAAAAAAA[-/AAAAAA]GACTTTATATGCCAG | 7468 |
| rs61464782 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959859 | TTTTTGGAAAAAAAA[-/A]TTTTTTTTGTTTTTG | 7468 |
| rs61535099 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894691 | AAAAAAAAAAAAAAA[-/A]TGAAAAGAAGAAGTT | 7468 |
| rs61664298 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934878 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 7468 |
| rs62286993 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885035 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 7468 |
| rs62286994 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889327 | GCTTCCTGAGTAGCT[G/T]GGACTACAGGCATGC | 7468 |
| rs62286995 | snp | A/G | 0.0333695 | 0.124785 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890778 | TAATTTTCTATTTTT[A/G]GTAGAGACGGGGTTT | 7468 |
| rs62286996 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890893 | TAAGCCACCACGCCC[A/G]GCCTTTTTTTTCTTT | 7468 |
| rs62286997 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897186 | AAGGAAAAAAAAAAA[A/G]GGAAAGTGGTTTGGG | 7468 |
| rs62286998 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898023 | TGCCTTTTTTTTTCC[C/T]TCCTCCTTCTGGGTG | 7468 |
| rs62286999 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902292 | GGCAGTGGTGTGATC[A/G]TGGCTCACAACAGCC | 7468 |
| rs62287000 | snp | C/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903999 | TTGGCCTCCCAAAGT[C/G]CTGGGACTACAGGCG | 7468 |
| rs62287001 | snp | G/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913152 | GAAGGGACACGGTGA[G/T]AAGTGACCAGAAGAC | 7468 |
| rs62287002 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915260 | AGCTGAGGCTACAGG[C/T]GCCCACCACCATGCC | 7468 |
| rs62287003 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916634 | GGCGTGAGGGACTGC[C/G]CCTGGCCTGGTTGGC | 7468 |
| rs62287004 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918138 | CTCTTTTTTTTTTCC[C/T]AGCTATTGAAACCAA | 7468 |
| rs62287005 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925641 | TGACCTCAGGTGATC[A/C]ACCCGCCTTGGCCTC | 7468 |
| rs62287051 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926573 | CCTTCCGGGTTCAAG[C/T]GATCCTCCCCCCTCA | 7468 |
| rs62287052 | snp | A/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937053 | TTTGCTCTGGTCACC[A/T]AATTTTTTTTTTTTT | 7468 |
| rs62287053 | snp | A/G | 0.0266679 | 0.112351 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956121 | GGCGCGAGTGTTCCC[A/G]TACATGGAGGGGGAC | 7468 |
| rs62287054 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976234 | ATGCTGCTGAGATGC[A/G]TCATTGCAGGCTTCC | 7468 |
| rs67346005 | snp | A/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934877 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 7468 |
| rs71167762 | in-del | -/CTCTCTCTCTCTCTCTCTCTCA | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872592 | TCTCTCTCTCTCTCT[-/CTCTCTCTCTCTCTCTCTCTCA]CACACACACACACAC | 7468 |
| rs71167763 | in-del | -/TGTGTGTGTGTGTGTGTG | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951507 | TTCCAACAGGAACTT[-/TGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 7468 |
| rs71223151 | in-del | -/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913197 | TTCACGCCCAGAGAA[-/G]GGCCGCTGGAGGGCT | 7468 |
| rs71589624 | in-del | -/A | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878284 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 7468 |
| rs71589625 | in-del | AA/TAT | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878256 | AAAAAAAAAAAAAAA[AA/TAT]ATATATATATATATA | 7468 |
| rs71606380 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915300 | TTTGTATATTTAGTA[A/G]AAATGGGATTTCACC | 7468 |
| rs71606381 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936553 | GTGCATGCCTGTAAT[C/G/T]TCAGCTACTCGGGAT | 7468 |
| rs71606382 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965481 | ATGGCTGAAAAATTC[C/T]CAGGTTTGATGAAAC | 7468 |
| rs71606383 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971408 | AGTGAATACAGCTGA[C/T]GGTGAGTTCACCTCT | 7468 |
| rs71606384 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971535 | GCAGAGACTTAGAGA[A/C]CAGAAACAATAGAAA | 7468 |
| rs71640395 | in-del | -/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894484 | TGAGACCAGCCTGGG[-/G]CAATGTGGTGAAACC | 7468 |
| rs71640396 | in-del | -/A | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902990 | ACTAGCCTGGGCAAC[-/A]ATAGCGAGACCCGGT | 7468 |
| rs71640397 | in-del | -/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902993 | AGCCTGGGCAACATA[-/G]GCGAGACCCGGTCTC | 7468 |
| rs71644316 | in-del | -/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902994 | AGCCTGGGCAACATA[-/G]CGAGACCCGGTCTCT | 7468 |
| rs71644317 | in-del | -/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909649 | ATCCTTTTTTTTTTT[-/T]CTTTTCCTGGAGATG | 7468 |
| rs71686652 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893661 | GGCTCAACTGATCCT[-/CCT]GCCACAGCCTCCCCA | 7468 |
| rs72598770 | in-del | -/GT/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873798 | AGCAAGAACTTAAAA[-/GT/TT]GAAGTGCTAAGATGG | 7468 |
| rs73069112 | snp | A/T | 0.039522 | 0.134904 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957810 | TTCATAGACTCTAGT[A/T]TTATGGGAACCAGAA | 7468 |
| rs73069117 | snp | C/T | 0.0177549 | 0.0925323 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974985 | TGTGGGCCTGTTTGC[C/T]GTCTGTGACATTCCT | 7468 |
| rs73202826 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881798 | TATAATAGGGAGGTT[A/C]TACCTGACAAGGCTT | 7468 |
| rs73202827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883260 | ATTAAGAAATAAAAA[C/T]TTGTGGACTTCCTTA | 7468 |
| rs73202828 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894621 | AGGATGCAGTGAGCT[A/G]TGATGGCACCATTGC | 7468 |
| rs73202829 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898707 | TTTTTTTTTTTTTTT[G/T]TCCAGCAGCTGGAAT | 7468 |
| rs73202830 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909164 | TTAAGTTCCTTTAAG[C/T]TGTATGCCTTTGACA | 7468 |
| rs73202831 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913306 | CCTGAGAAGGCACCC[A/G]TTACTTTGCAAACCA | 7468 |
| rs73202832 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928684 | GCAGTAAAGGACACT[C/G]TTAGCATTCATCCTA | 7468 |
| rs73202833 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956840 | GGTCAGTGCTGGCTC[C/T]TGTGTGACTGCAGGC | 7468 |
| rs73202834 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958637 | GTGATAAGTGTGTGC[C/T]GGAGGTCAGGTGCTC | 7468 |
| rs73202835 | snp | C/G | 0.153665 | 0.230694 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971073 | AAAAATAAAATTGTG[C/G]GCAGGCCGGGTGCAG | 7468 |
| rs73202836 | snp | A/T | 0.0262144 | 0.111504 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978619 | CTTCTGTGTGCTCAC[A/T]TCTTGTGTTCTGTTG | 7468 |
| rs73202837 | snp | G/T | 0.084728 | 0.187577 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979502 | CCTAGTGAGAAGCTG[G/T]CCCTGCAGGTGGTGG | 7468 |
| rs73796606 | snp | A/C | 0.0524604 | 0.153226 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903661 | TAGATTTATATAGAG[A/C]TCTTCAAAATGTTGA | 7468 |
| rs73796607 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904112 | ACTCCATTTTTGGGG[G/T]TCTGTGTGTATTTGG | 7468 |
| rs73796608 | snp | A/T | 0.0172755 | 0.0913198 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904425 | TTCTCTTCTGCACTT[A/T]ATCTTTCTCATCTCC | 7468 |
| rs73796609 | snp | C/T | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904562 | TATTCAACTCAAATA[C/T]GTACTTCATCTGATT | 7468 |
| rs73796611 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939013 | ATAAGAGGGGAAATT[A/G]CACTTCCTTTTACCT | 7468 |
| rs73796613 | snp | C/T | 0.103794 | 0.20279 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944397 | AGAACCTCAAAATAA[C/T]GGTGATACATTCTAG | 7468 |
| rs73796614 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951319 | CTTCCCCAATCTCAC[C/T]GTCACTCACTCATCT | 7468 |
| rs73796670 | snp | C/G/T | 0.00376034 | 0.0431981 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960994 | ACACTGAGGATTGGT[C/G/T]AGCACGCTTTTTGTC | 7468 |
| rs73796671 | snp | C/T | 0.124837 | 0.216412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964507 | GTTCTTGGAGCACCT[C/T]GCACACAGCTTGAGG | 7468 |
| rs73796672 | snp | A/G | 0.124144 | 0.21601 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971570 | TAAATCTCTTCTTAC[A/G]AGCCCACAATAGTGC | 7468 |
| rs73796674 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977182 | ACCAGGAGGCTCCGC[C/T]GGTTGACGAAGGAGC | 7468 |
| rs73796676 | snp | C/G | 0.0569829 | 0.158885 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981642 | GTCCGTCCTCAGGCC[C/G]GCCTTTCTTCCGGCG | 7468 |
| rs73799026 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883676 | CCGCTCTGCTGATCC[C/T]ACCTTGTTTGTTGTC | 7468 |
| rs73799028 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887081 | TTGTAAGTGGGACAT[A/G]GTTTGCCAGGGTTAG | 7468 |
| rs73799029 | snp | G/T | 0.0678174 | 0.1712 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891524 | GCCAGTGGGCAAGGT[G/T]GGAGCAGTGAGGCCT | 7468 |
| rs74282798 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912936 | GTGCCMAGGCAAGAG[A/C]CTGAAGGCACAGGCT | 7468 |
| rs74332369 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891869 | CTCAAAAAAAAAAAA[-/AAA]CAAAAAAAAACAAAC | 7468 |
| rs74372602 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980595 | TTTGTGACCTGTAAG[C/T]GTGGGGTTCAGGGGT | 7468 |
| rs74373191 | snp | A/G | 0.021333 | 0.101051 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917152 | TGTAATGGCTTAACA[A/G]TCTCTTTCATTGTTG | 7468 |
| rs74375029 | snp | A/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889822 | GACCTTTTTTTTTTT[A/T]AATTGAGATAAAATT | 7468 |
| rs74431689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961229 | TGTAGAACTGGACTT[C/T]GCCCTGTGGCAGCGC | 7468 |
| rs74432689 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908289 | TAGCTTTGGCCCTTT[A/C]CTAAAGATCTGTGTA | 7468 |
| rs74623987 | in-del | -/AA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949780 | AGAAAAAAAAAAAAA[-/AA]GCCCACTCTAACACT | 7468 |
| rs74641500 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894545 | AGTGTGGTGGTGCAT[G/T]CCTGTATTCCCAGCT | 7468 |
| rs74661485 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890288 | TGTACAAGTTTTTTT[G/T]GTTTTGTTTTGTTTT | 7468 |
| rs74665455 | snp | C/T | 0.00275062 | 0.036983 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900882 | GCCCTTTATTCCAGC[C/T]GACAAGCTGAAAGAT | 7468 |
| rs74697571 | snp | A/G | 0.029116 | 0.117091 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944573 | CTTGAGGCATTCACT[A/G]GAGGTGAAAACTTGT | 7468 |
| rs75139506 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909079 | TCCCTAAAAAAAAAA[A/G]AGTTATATATTTTAG | 7468 |
| rs75166276 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896135 | TCTAGTCCAGACAGC[A/C]GCTCCACACTTGGTG | 7468 |
| rs75198787 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896681 | CTCCCTCCCTCCCTC[C/T]CTTCCTTCCCGAACT | 7468 |
| rs75251058 | snp | A/C | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966656 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 7468 |
| rs75274604 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878686 | ATGTCCCAGAAATGG[G/T]GTGAATGAAGGGGAG | 7468 |
| rs75288714 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966658 | CAAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 7468 |
| rs75304584 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975664 | GGGTGTGGGCAGGGC[C/T]GTGCGCCCTCTGAAG | 7468 |
| rs75345749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886124 | GTATGCTTTGTGAGT[C/G]TTGTAATCAAAGGTG | 7468 |
| rs75348304 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944241 | GGAGCGGAGTTTTCC[A/G]AGAGGACCATCTCCT | 7468 |
| rs75645807 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909078 | CTCCCTAAAAAAAAA[A/G]GAGTTATATATTTTA | 7468 |
| rs75646793 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909833 | TTTAGTAGAGCTGGG[G/T]TTTCACCATGTTGGC | 7468 |
| rs75774205 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877141 | GATTCTGTCTCAAGG[A/G]AAAAAAAAAAATTGT | 7468 |
| rs75814052 | snp | A/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876752 | GGTGTGTAGAAAAAA[A/T]GCTTTTTTTTTCTGG | 7468 |
| rs75820801 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889879 | TATAGAGTGTACAAT[C/T]CAGTGGTGTTTTTGG | 7468 |
| rs75942149 | snp | G/T | 0.0744748 | 0.178019 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957828 | ATGGGAACCAGAAAC[G/T]ATACTTAACATTGAA | 7468 |
| rs75949599 | snp | C/T | 0.00634778 | 0.0559785 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978711 | TTGCCACCTCTGCCC[C/T]AATTCGTTCTGTAAG | 7468 |
| rs76187446 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877139 | GAGATTCTGTCTCAA[A/G]GAAAAAAAAAAAATT | 7468 |
| rs76268244 | snp | C/T | 0.105214 | 0.203807 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898723 | TCCAGCAGCTGGAAT[C/T]TCTTTTCAGTTATTT | 7468 |
| rs76269136 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889226 | TTTTGAGACAGGGTC[G/T]TCTTCTGCCACTCAG | 7468 |
| rs76346200 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970842 | GCCAACAGGACAGGA[C/T]GGAGTCCCCAACAGC | 7468 |
| rs76349520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949909 | AGGTCACAGGATTGG[G/T]CAAGAGTCCCTGGTG | 7468 |
| rs76358965 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978425 | CGCTAACAGGTGGTC[C/T]TTAGGGGCCTGGCAG | 7468 |
| rs76383516 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974227 | AGTCTTTTTTTTTTT[G/T]GAGACGGAGTTTTGC | 7468 |
| rs76431401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973820 | AACACGTGACTGTTA[C/T]GCTTTATGTGGCCTT | 7468 |
| rs76475197 | snp | C/G/T | 0.0252325 | 0.109451 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971626 | CTGAGGCGTGAGGTC[C/G/T]GAGCCAGGGCGTGGA | 7468 |
| rs76729008 | snp | C/T | 0.0441095 | 0.141807 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947844 | GTGAAGGGATTTGTT[C/T]TGTCAAAAAATTAAA | 7468 |
| rs76747887 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885111 | GCAAAACTCTGTTTC[A/C]AAAAAAAAAAATAAA | 7468 |
| rs76768118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957558 | CTCCCAAAGTGCTTC[A/G]ATTACAGGCGTGAGC | 7468 |
| rs76803790 | snp | G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925417 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTTGCT | 7468 |
| rs76833016 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942096 | GGTTGGTATTTCAGA[A/G]CACTTTAGGTCATGT | 7468 |
| rs76860793 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880758 | AGACCAGTAAGCCAT[A/G]CTCATCAACAGGGAA | 7468 |
| rs76923105 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960577 | GAGTTCATAAGCCTG[C/G]TGCCAGTTCCAGCAA | 7468 |
| rs76949546 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946699 | AATTACCACTAATTT[A/T]CCTGGCAGTGATGTC | 7468 |
| rs77067799 | in-del | -/AA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905133 | GAAACTCTGTCTCAC[-/AA]AAAAAAAAAGAATGT | 7468 |
| rs77074637 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980047 | GAAGATGCAGTCTCT[C/G]CTGATCACATGTGCC | 7468 |
| rs77154471 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886837 | AGCGAGACTCCATCT[A/C]AAAAAAAAAATAACT | 7468 |
| rs77241267 | snp | C/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923891 | ATGCAGATTCTATCA[C/G]TTGTGTAGTTTGAAA | 7468 |
| rs77258201 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940546 | GTTTCCTGATTTTTA[A/G]GGATTACCTTCATAG | 7468 |
| rs77280245 | snp | A/G | 0.00801454 | 0.0627936 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901285 | GTAAGGGGTCATGTG[A/G]CCTTGAGCAGTGAGC | 7468 |
| rs77325279 | snp | G/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937070 | ATTTTTTTTTTTTTT[G/T]AGAGGGAGTCTCACT | 7468 |
| rs77325873 | snp | C/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907841 | TGATCTTGATCTCTT[C/G]ACCTTGTGATCCACC | 7468 |
| rs77438375 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932508 | TCCCAGCACTTTGGG[A/G]GGCCGAGGTGGGCAG | 7468 |
| rs77441783 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1948867 | TCCATGCATTTTTTT[C/T]CTCATTTTTAAAGCT | 7468 |
| rs77443625 | snp | A/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887338 | CTTCTTTTTTTTTAA[A/T]TCTCCCTTGCTCAGT | 7468 |
| rs77512331 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898074 | TTGTTCCACAGATCT[C/G]TGAGGCTCTGCTTCC | 7468 |
| rs77514933 | snp | G/T | 0.118933 | 0.212888 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921350 | TGTACTTCCGGCTAT[G/T]TGGGAGGCTGAGGCA | 7468 |
| rs77520268 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981688 | TGGCTGGGTCCCCTT[C/T]GCAGTGTTTGTCTGT | 7468 |
| rs77523305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905370 | CTCTGGAAGTGTGGC[A/G]TCTAGAGTCAGGCCA | 7468 |
| rs77556490 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962529 | AGGATCGGGAAAAAA[A/T]TTGTGTGTGTATACA | 7468 |
| rs77607221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892485 | ATTAGTTATATAATT[C/T]CTAAGCACTTATTTT | 7468 |
| rs77626068 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956923 | AGGCTGCACTGAGTG[A/G]TAGGAGTGCATGGTG | 7468 |
| rs77645399 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914818 | ATTTCTTGTTCCATT[A/G]ACTTGGAGGCTGGCC | 7468 |
| rs77649910 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888135 | TAAGGCTATATGGCT[G/T]GGTGCGGTGGCTCAC | 7468 |
| rs77808487 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888436 | AAAAAAAAAAAAAAA[A/G]AGACTTTATATGCCA | 7468 |
| rs77875172 | snp | A/T | 0.124491 | 0.216211 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897645 | TTTATTTTTATTGAT[A/T]TATTTTTGAGACAGA | 7468 |
| rs77972341 | snp | G/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957301 | TTGTTTTTTTTTTTT[G/T]GAGACTGAGTCTTGC | 7468 |
| rs77973131 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893471 | GAGACTCCGTTTCAA[A/T]AAAAAAATAAATAAA | 7468 |
| rs78001738 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893472 | AGACTCCGTTTCAAT[A/C/T]AAAAAATAAATAAAT | 7468 |
| rs78013085 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971357 | ACCCTAAATTTAGGG[C/T]CTTCCCACTGGCCTA | 7468 |
| rs78069264 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916150 | TCTAGCACTGTGAGA[G/T]AGGGGGGTAGCTAGC | 7468 |
| rs78109580 | snp | C/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870351 | TGGGCCTGTAAAGCT[C/T]GAGCAGACACTAAGG | 7468 |
| rs78128368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917257 | TTGATGACTCTCAGA[A/G]ATAACTTGTTTTAGA | 7468 |
| rs78158789 | snp | A/C | 0.00109531 | 0.0233764 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930810 | CCTCTGCTTGGGTTG[A/C]TGTGTGTAGTGTAGC | 7468 |
| rs78200706 | snp | C/T | 0.116138 | 0.211142 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872470 | TGCAGCACGAATCTT[C/T]CTGTGCCCACGATGG | 7468 |
| rs78264453 | snp | A/G | 0.105569 | 0.204058 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881920 | TATCAGATGGAGGGA[A/G]GAGCCTGTGCAGAGC | 7468 |
| rs78285285 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921693 | AGGTTGAGAAAGGAG[A/G]ATCGGTTGAACCTGG | 7468 |
| rs78296547 | snp | A/G | 0.067446 | 0.170804 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917297 | TACACATATATGTAC[A/G]TATATATGTGTATAC | 7468 |
| rs78328023 | snp | A/G | 0.0577344 | 0.159793 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948064 | GAGACTGCATTCCCT[A/G]CCCTGAAGGAATGTA | 7468 |
| rs78373478 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886483 | AAGTTCTGGGATTAC[A/G]GACTTGAGCCACTGT | 7468 |
| rs78424138 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876755 | GTGTAGAAAAAATGC[C/T]TTTTTTTTCTGGAAG | 7468 |
| rs78441255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934233 | TGAGATTACAGACAT[A/G]TGCCACCATGCCTGG | 7468 |
| rs78441555 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876764 | AAATGCTTTTTTTTT[C/T]TGGAAGGAATTGGAA | 7468 |
| rs78479906 | snp | C/T | 1.64917e-05 | 0.00287151 | missense | WHSC1 | GRCh38.p7 | 4:1901004 | CTAACACTACCCCTA[C/T]CAAAAATGGCTCTCC | 7468 |
| rs78610521 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924451 | TTGTGAAAAAAATGG[A/G]TACCTGAGAATTGAA | 7468 |
| rs78629684 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936224 | GGTTATTCTGTCTAG[C/T]GTATGGTGCCCATGC | 7468 |
| rs78685951 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924220 | ATCAGCAATGTGTGT[A/T]CAGCCACCGTTTCAG | 7468 |
| rs78721382 | snp | A/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894692 | AAAAAAAAAAAAAAA[A/T]GAAAAGAAGAAGTTG | 7468 |
| rs78808211 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967070 | GACTCACATAACTAA[A/T]ATCAGAACTGGGTGT | 7468 |
| rs78845204 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939288 | AAGTGTGGGAGTAGC[A/G]TTGTGGTTATATGTA | 7468 |
| rs78871981 | snp | A/G | 0.0387552 | 0.1337 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948315 | GATATGGAATAGATC[A/G]TAGATGTTGTAGACT | 7468 |
| rs78963716 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940517 | TGACACTTTTTTGTT[C/G]GGAGGTAGTTTTGGT | 7468 |
| rs78968817 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968220 | TTGAATGTCAGAAGT[G/T]AAATGTGAGATCCAA | 7468 |
| rs78970451 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883630 | AGCAAGACTTTGTTT[A/C]CAAAAAAAAAAAAAA | 7468 |
| rs79109878 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975899 | ACAATGACCCTATTT[C/G]CAAATACAGTCACCT | 7468 |
| rs79111758 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955556 | ATGACATTTGCTCTC[A/G]TGCTGATGTACAGAT | 7468 |
| rs79256228 | snp | G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917794 | TTTTTTTTTTTTTTT[G/T]TTTTGAGACAGGGTC | 7468 |
| rs79341449 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921783 | CAAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 7468 |
| rs79375419 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928084 | TTCTTTTTTTTTTTT[C/T]TTCAAACACGATCTT | 7468 |
| rs79385915 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898705 | CTTTTTTTTTTTTTT[-/TT]GTCCAGCAGCTGGAA | 7468 |
| rs79402980 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898139 | TAATCCAGGTTGGAG[C/T]GCAGTAGTGCAATCA | 7468 |
| rs79404586 | snp | C/G | 0.0652144 | 0.168387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967305 | TCCTGAGAGGCCGGG[C/G]ACGGTGGCTCATGCC | 7468 |
| rs79408412 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877550 | CCCCATGTGTTTGGG[C/G]GATAGGCATGCTTTC | 7468 |
| rs79500499 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976017 | CGGTGGCACCAGCTC[A/G]GCCCTGAGCCGGTGT | 7468 |
| rs79595086 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886071 | ATATTTTCTGCTTAT[A/C]TTTTCCTTTACGAAA | 7468 |
| rs79653189 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921107 | GAACTTCCTAAATCT[G/T]TTTAAGGATATGTAT | 7468 |
| rs79663895 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876401 | CTCAGCTCAAAAACT[C/G]CAGTAGTGGATAGGC | 7468 |
| rs79692643 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977792 | GCAAGACTCCACTCA[A/C]AAAAAAAAAAAACCA | 7468 |
| rs79705811 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925342 | GCTGACTTCAGGACT[G/T]TTTGTTGCTACTTGC | 7468 |
| rs79740090 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886482 | AAAGTTCTGGGATTA[C/T]GGACTTGAGCCACTG | 7468 |
| rs79768526 | snp | A/T | 0.030665 | 0.119967 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897321 | ATCCATCTCTACAAA[A/T]AAAGGGTTAAAAAGT | 7468 |
| rs79783341 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975895 | ATTGACAATGACCCT[A/C]TTTCCAAATACAGTC | 7468 |
| rs79837086 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876307 | GAGTTTTCAAAGCAT[A/T]TTACTTTCTGTAATA | 7468 |
| rs79935477 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972007 | CACGCCGCTCCTGTA[C/T]CCCCAAGGCTGCGGG | 7468 |
| rs79990672 | snp | G/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933567 | GCTAATTTTTTTTTT[G/T]GTATTTTTAGTAGAG | 7468 |
| rs80157840 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883648 | AAAAAAAAAAAAAAA[A/G]AGCGTACCTCCTCCG | 7468 |
| rs80171018 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939215 | TTAAAAAAAAAAAAA[A/G]ACATGAGCAATTGGA | 7468 |
| rs80265873 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921690 | GAGAGGTTGAGAAAG[A/G]AGAATCGGTTGAACC | 7468 |
| rs80330542 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960574 | AGAGAGTTCATAAGC[C/G]TGGTGCCAGTTCCAG | 7468 |
| rs111257046 | in-del | -/CTC | 0.00239313 | 0.0345085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975282 | TTTGGTGTCTGTCTC[-/CTC]TTCTCCCAGGGACGG | 7468 |
| rs111264375 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899477 | AACAAAATCCTCCCC[A/G]TTTGAGAACCGCTGT | 7468 |
| rs111266494 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916161 | GAGATAGGGGGGTAG[C/G]TAGCTGGTAGGTAGC | 7468 |
| rs111298117 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967307 | CTGAGAGGCCGGGCA[C/T]GGTGGCTCATGCCTG | 7468 |
| rs111365994 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1871019 | GGCTCGGGGGCGCCG[A/G]CTCCGGACGGTGATT | 7468 |
| rs111398358 | in-del | -/AAAA | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977790 | AGCAAGACTCCACTC[-/AAAA]AAAAAAAAAAAAAAC | 7468 |
| rs111407761 | snp | A/T | 0.155656 | 0.231515 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934910 | ATATATATATATATA[A/T]AAAACAGATAAAACA | 7468 |
| rs111467018 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962807 | TCCTGAGTATCTGGG[A/C]CTACAGGAACATGCC | 7468 |
| rs111497414 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952612 | ACCTGGTTGGTCACC[A/G]AACACTGAAGTCCAT | 7468 |
| rs111535511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905297 | CAAGTTGCGATGTGG[C/T]GAGTGCGGAGTTAGA | 7468 |
| rs111549334 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913781 | AGTCTCCGCATCTTG[A/G/T]TGGTAGTGGTGTCCC | 7468 |
| rs111584556 | in-del | -/TGTATTCGAAG | 0.184203 | 0.241186 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966046 | CAGGCAGTGGGCCAA[-/TGTATTCGAAG]TGCTAAAAGAAGAAA | 7468 |
| rs111668967 | snp | A/T | 0.0283406 | 0.115616 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979994 | TCTCCTGCCACCCAG[A/T]GTGGCTTCCATCTCA | 7468 |
| rs111700375 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966638 | CTCCAGCCTGGGTGA[C/T]AGAGCAAGACTCTGT | 7468 |
| rs111715175 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934973 | TCACCAGTTTTTTTG[C/T]TGTAAAGAGATTTGA | 7468 |
| rs111728006 | snp | G/T | 0.0577344 | 0.159793 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891669 | CATCCTGGCTAACAT[G/T]GTGAAACCCCATCTC | 7468 |
| rs111735900 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975469 | CCTGGAGACCTGTGT[C/G]CCCCGTGAACAGCGG | 7468 |
| rs111744939 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960727 | GTTGTGGGGATCACC[C/G]TGTAAAGTGGGTTAT | 7468 |
| rs111759681 | snp | A/C | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930292 | ACTGGCTCTACAGCT[A/C]ATTTTTCAGGGGTGC | 7468 |
| rs111803920 | snp | C/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894239 | TGGGATTACAGGTGT[C/G]AGCCACCACGCCTGG | 7468 |
| rs111814249 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958872 | AAAGAGTGTCTTTCG[C/T]CACCTCTTCCCTAAG | 7468 |
| rs111917798 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946799 | AAGGAGCATGCTTCC[C/T]TTGGGACATTCTTAC | 7468 |
| rs111994664 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907149 | CTTCAGTTTCCCTGT[A/G]TATGAAAATGAGGAA | 7468 |
| rs112001707 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878035 | CTGTCCCAAAAGAAA[A/G]ATAAAATTTAAAAAA | 7468 |
| rs112014939 | snp | A/G | 0.00352293 | 0.0418217 | missense | WHSC1 | GRCh38.p7 | 4:1918543 | CCTGGGAGGAAGAAG[A/G]CCACAGTCTCCATGC | 7468 |
| rs112015057 | snp | G/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957288 | TGTTTTTTTGTTTTT[G/T]TTTTTTTTTTTTTGA | 7468 |
| rs112078240 | snp | A/C | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870913 | CCTCCCGCGGGCCCC[A/C]GGCCCCGCGCCCCTC | 7468 |
| rs112146288 | snp | A/G | 0.0463947 | 0.145069 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979433 | TCTTTGGAAATGGCT[A/G]TATCATTTTTTTGTA | 7468 |
| rs112168336 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925202 | TTTTCGGGAGTGCTG[A/G]TGCACACAAGGATGG | 7468 |
| rs112199742 | snp | A/C | 0.5 | 0 | missense | WHSC1 | GRCh38.p7 | 4:1975302 | CTCCCAGGGACGGAG[A/C]TGACTTTTAACTACA | 7468 |
| rs112200469 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930326 | GAGGCTGGGTCTTAA[C/G]TGAGTTAGTGGTTTT | 7468 |
| rs112201737 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934200 | AAGCGATTCTTCTGC[C/T]TCAGCCTCCTGTGTA | 7468 |
| rs112238235 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894487 | AGACCAGCCTGGGCA[A/T]TGTGGTGAAACCCCG | 7468 |
| rs112361507 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967890 | GAAAACAGGAATTAG[A/G]GAGGGATAAGGAAAG | 7468 |
| rs112361822 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930058 | GGGTGCTGATGCTGG[C/T]AGCCCTGGTGTGGCT | 7468 |
| rs112372308 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898906 | AATGGAGTTCACCCA[A/G]TGCTGTTCCCTTTCT | 7468 |
| rs112393759 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965551 | GATGATCAAACTTTC[A/G]AAAACCAGAAAAAGA | 7468 |
| rs112412498 | snp | A/G | | | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952115 | CCCCGCAGCTGTGTG[A/G]GAAGCCGGGCAGCCT | 7468 |
| rs112425353 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966374 | ATGATTGAAGAGATA[C/G]GGCTGGGCATGGTGG | 7468 |
| rs112427041 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976956 | GGCCCAGCTGCAGAA[C/T]TGGGGCCCTCATCCA | 7468 |
| rs112451163 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918858 | TGGATAAGAAGATAC[C/T]GAGAACAGGCCAGGC | 7468 |
| rs112465621 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882292 | CTTCTGAGTGGAAGC[A/G]CTGAGACACGTGCTT | 7468 |
| rs112550730 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970034 | GAAAGAACCTGGGAA[-/AG]AGAGAAAGAAGGAAT | 7468 |
| rs112552381 | snp | A/G | 8.28397e-05 | 0.00643529 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975052 | TGGCTATGGGGGCAG[A/G]GTGGCCATCGCTGAG | 7468 |
| rs112586954 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921455 | AGAGCGAGACTCCGT[C/G]TCAAATTAAAAAAAA | 7468 |
| rs112645710 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923692 | GATGTGCCTTTTTTT[C/G]TCTTACAGTTTTACT | 7468 |
| rs112691599 | snp | C/T | 0.0166325 | 0.0896639 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981543 | ACCCGTGTGCGCCCA[C/T]AGGGGGATGTGTCCG | 7468 |
| rs112710017 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974216 | TCGGTTGGGTGAGTC[-/T]TTTTTTTTTTTGAGA | 7468 |
| rs112748858 | in-del | -/A | 0.0926964 | 0.194308 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978126 | GCTAGACTCCATCTC[-/A]AAAAAAAAAAGAATT | 7468 |
| rs112794510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917194 | AGGATGCCATGTTAC[A/G]ATATGATAAAGTTCT | 7468 |
| rs112803089 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1954910 | TGCACAATGCCCAGG[A/T]CGGCTGCCCACGTGC | 7468 |
| rs112833463 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967583 | ACTTTGTCTCAAAAA[A/G]AAAAAAAAAGATATT | 7468 |
| rs112889000 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905913 | AAAAAATAAATGCTG[A/G]TTGAGACAGAAGCTG | 7468 |
| rs112893919 | snp | A/G/T | 0.000219524 | 0.0104746 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904201 | TAGTGTTTGTCTTCT[A/G/T]TTGTTCATTTTCAGA | 7468 |
| rs112939388 | snp | C/G | 0.00339144 | 0.0410392 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900870 | CCACGACGCCCTGCC[C/G]TTTATTCCAGCCGAC | 7468 |
| rs112973595 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1871369 | GCGGCGGCGGCGGCG[G/T]GCGGGAGGCGCGGGG | 7468 |
| rs112996333 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977584 | AGTTCGAGACCAGTC[C/T]GACCAACATGGTGAA | 7468 |
| rs113032773 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977189 | GGCTCCGCCGGTTGA[C/T]GAAGGAGCTGCAGCT | 7468 |
| rs113037688 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880685 | TACAGGAAATACAGG[A/G]GCAAGAGAAATACTA | 7468 |
| rs113042971 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952867 | CTCACGTCAGAACAC[C/T]TCCTGGGTCAGGAAG | 7468 |
| rs113085953 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911357 | CTTTGGGAGGCCAAG[A/G]CAGGTGGGTGACTTG | 7468 |
| rs113099294 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896589 | CAGGCTCATCTCAAA[A/C]TGCTGGGTTCAAGCA | 7468 |
| rs113101869 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913821 | GCTGTCTTTTCTTCA[A/G]TCTCTTTGTCTTGTG | 7468 |
| rs113166498 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974156 | TCTCCACCTCTGCCT[A/G]GATTTGCTCTTTGGG | 7468 |
| rs113238906 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978381 | CTGCACCCGGCACAG[C/T]TCCTCTCAGTTGCCG | 7468 |
| rs113253323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960741 | CGTGTAAAGTGGGTT[A/G]TGTAGAAGCTTGGTT | 7468 |
| rs113260836 | snp | A/G | 0.046775 | 0.145601 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935747 | GCACCTGTAATCCCA[A/G]CTACTCAAGAGGCTG | 7468 |
| rs113264347 | snp | A/C | 0.00039992 | 0.0141351 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924755 | CATCTCTACAAAAAA[A/C]AAAACAAAACAAAAC | 7468 |
| rs113265312 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903859 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGATTA | 7468 |
| rs113266535 | snp | A/T | 0.0759472 | 0.179459 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891875 | AAAAAAAAAAAACAA[A/T]AAAAAACAAACAAAA | 7468 |
| rs113311006 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969262 | GCAGAGAGAAAGGGA[C/T]CTGAGGCTCTGAGGG | 7468 |
| rs113331586 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904973 | GCGTCTCTACTAAAA[A/G]TACAAAATTAGCCGG | 7468 |
| rs113466969 | in-del | -/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934027 | GTTGTTTTTTTTTTT[-/T]AAGTTCAACTTAAAT | 7468 |
| rs113471400 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926450 | GAGCCACCGTGCCTG[A/G]TTTGGCTTGAATTTT | 7468 |
| rs113537314 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965989 | ACAAGGGATTCTCAA[G/T]GAGATTATCAGCAAA | 7468 |
| rs113539527 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1890151 | AGCATAAATCAGGAC[A/G]TCATTTCTTTTTGTG | 7468 |
| rs113539879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907035 | TTGTGCTTATGGCAC[C/T]GTTGTGTTACTCTCT | 7468 |
| rs113620286 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910649 | TGCTTCTGGCATTTT[C/T]TAAAAATATTGCAGG | 7468 |
| rs113623930 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892001 | ATGCTTTCTCTTTTC[C/G]TAGCATATCTACTCT | 7468 |
| rs113627824 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889189 | AGGCGTGAGCCACTG[C/T]GCCCAGTCGTATATT | 7468 |
| rs113633959 | snp | G/T | 0.00543122 | 0.0518277 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957891 | GAAAGGTAGTTACCT[G/T]TATTTACTAAAATCT | 7468 |
| rs113648846 | snp | C/T | 0.128632 | 0.218563 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898380 | CCTTAAAAATGGTTT[C/T]GTGGCCAGGTGCGGT | 7468 |
| rs113658185 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888141 | TATATGGCTGGGTGC[A/G]GTGGCTCACGCCTGT | 7468 |
| rs113706511 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893817 | CCCAAAGTGTTGGAA[C/T]TGCAGGTGTGAGCCA | 7468 |
| rs113712964 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953794 | TTTGTTTACCCTGGC[-/T]TTTTTTTTTTTCTTT | 7468 |
| rs113753572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875468 | TGTGTTTTATACAGA[C/T]AGGATTTCACCATGT | 7468 |
| rs113840011 | snp | C/T | 5.08212e-05 | 0.00504064 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930792 | ATAGCATTATGCTGA[C/T]GTCCTCTGCTTGGGT | 7468 |
| rs113867863 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941881 | TTCCAATGCTGAATG[C/T]CTGTTAGCATATGAG | 7468 |
| rs113873454 | snp | G/T | 0.227664 | 0.249 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893555 | TTTGTTTTTTTTTTT[G/T]TTTTGTTTTGTTTTG | 7468 |
| rs113887663 | snp | G/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881883 | GGGGATTGGGTGTTG[G/T]CTCCATGAGGGTGGG | 7468 |
| rs113925680 | snp | A/G | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908729 | CCCATTGTCACTAAT[A/G]AGGGACCTGTGGGCT | 7468 |
| rs113937551 | snp | C/T | 0.5 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925394 | CTTTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 7468 |
| rs114085362 | snp | A/G/T | 0.0260105 | 0.111035 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979205 | GTTCCCTCCCACTCT[A/G/T]TTTTTTTAGGTTAAA | 7468 |
| rs114089487 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962018 | ATAGAAAATGATCAC[C/T]GATAAAAAAATGTTG | 7468 |
| rs114094836 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958444 | GCAAGATGGCGGGGC[A/G]GCAGGGGAGCTTGCC | 7468 |
| rs114137808 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942785 | GTGGAAAATATCAGC[A/G]TCGCTACCCTCAGAA | 7468 |
| rs114143061 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879646 | ATCTCATCATGCTGC[C/G]TGTAGCTCTTGTGAT | 7468 |
| rs114163403 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876859 | TGCCGTTTGCTGGTG[C/T]GGTGGGTGGCTCACG | 7468 |
| rs114209896 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | WHSC1 | GRCh38.p7 | 4:1890096 | CATGTGGCCTTTGTA[C/T]CTAGCTTCTTTCACT | 7468 |
| rs114244464 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965966 | GGGACACAAAGCTAA[A/G]TCATATCACAAGGGA | 7468 |
| rs114244559 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886258 | GTGGCCAGGGCTGGA[G/T]TGTGGTGGTATGATC | 7468 |
| rs114260834 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937453 | AAAAAATACATGACC[C/T]TAGACACTCAGAATA | 7468 |
| rs114308800 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878911 | CCATAGCGTGAGAGT[A/G]GTGCAGGAGAGGGTC | 7468 |
| rs114315137 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922018 | CCAGGCGTGGTGATG[C/T]GCGCTTGTAATCCCA | 7468 |
| rs114316691 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912435 | ACCAAGTTATGTTCT[A/G]TAATTGCATTTTCTT | 7468 |
| rs114320665 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972405 | ATATACCTGGACAGG[C/T]AATTTCAAAGTCCAT | 7468 |
| rs114406880 | snp | A/T | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951830 | TTCAAATCTGATTTG[A/T]AATATCTTGGATGTA | 7468 |
| rs114422098 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964978 | AACAAAAACAGCAAA[C/G]CTAGGGCAAGGGGAG | 7468 |
| rs114446218 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873268 | CCTGACTGCATTAAT[A/G]CCAGAGTCTGGCCTC | 7468 |
| rs114476127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908756 | GGCTGTGCTTGTAGT[A/C]TGTCCCAACAGTGTA | 7468 |
| rs114486567 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919236 | GCGCTTTGCTTGAAG[C/T]GTGTGGTCATGTCCT | 7468 |
| rs114564019 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967920 | GGGAGTTGGTCAACA[A/G]GCAGCACGTGGTCAG | 7468 |
| rs114616446 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941503 | GCCTAGGCAGTTGTC[C/T]TGACCTTGAGAAGAC | 7468 |
| rs114728242 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899488 | CCCCATTTGAGAACC[A/G]CTGTTCTAGTCCACG | 7468 |
| rs114753785 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885146 | AAAAAAATAAAATTC[A/C]ACTGCCTGTAACTCC | 7468 |
| rs114758993 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964618 | ACAGAGGTGCAGACA[A/G]AGAGGTGCGCTGCGC | 7468 |
| rs114792920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1893907 | CACTTGTGGTGGCAC[A/G]AGGTGGGCATTTATT | 7468 |
| rs114883490 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979076 | CACTGAGCCATCCTC[A/G]GCAGCGTCCGCTGCG | 7468 |
| rs114943300 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928307 | TATATCTAGTACTCC[C/T]CAGAATCACCTTATA | 7468 |
| rs114949689 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955445 | TTCATTGATGTTGAC[A/G]GTGTTCTGTGCGTCT | 7468 |
| rs114982336 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878592 | ACCTGGAATGGTACC[G/T]GAGTGACTGTCAGGC | 7468 |
| rs114996966 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880452 | TGGCAGTGTACTTCT[A/G]CCTGATATTTCTTCA | 7468 |
| rs115007441 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877803 | ATCTGTGTGGCTTAC[C/G]CCTCACCCTCCTTCA | 7468 |
| rs115019641 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898719 | TTTGTCCAGCAGCTG[A/G]AATCTCTTTTCAGTT | 7468 |
| rs115033112 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968778 | TGTAGTTATTGGGGT[A/G]GAGGAGACACAGGAG | 7468 |
| rs115115779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900341 | ATGTGTCCATGGCCA[C/T]ACTGTAGATTATTAG | 7468 |
| rs115126819 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919804 | AGCTGGGCATGGTGA[C/T]GCGTGCTTGTAATCC | 7468 |
| rs115141675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880472 | ATATTTCTTCATTCA[C/T]TGAGTATCAGTTGTG | 7468 |
| rs115213539 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972851 | TGGGAAAGTTTTTGA[C/T]ACATTTTTTTTTCTT | 7468 |
| rs115214623 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933433 | GCTCTGTCGCCCAGG[C/T]GGCTGGAGTGCAGTG | 7468 |
| rs115273406 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906446 | GGGTTTCACCATGTT[A/G]CCCAGTTGGTCTCAA | 7468 |
| rs115391423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899950 | GATTAGTGGACTGAG[A/G]TAAGAATACTGGGTT | 7468 |
| rs115476134 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981004 | CAAAAGATCCCTTCC[A/G]GCAGGTAAGGGACTA | 7468 |
| rs115476405 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909212 | GAGCACCTCTTTACG[C/T]TCTGGTACAACAAGA | 7468 |
| rs115478404 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909662 | TTTCTTTTCCTGGAG[A/G]TGGAGTCTTGCTCAC | 7468 |
| rs115482265 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885507 | TCTGAGGTAAAGGAA[A/G]TCTGTCTCAGTGGCC | 7468 |
| rs115484121 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962001 | TAGTGCTTGAAAACC[A/G]GATAGAAAATGATCA | 7468 |
| rs115487829 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976062 | GTTGCTGAGGATGGT[C/G]ACTGCCCTCAGGTCA | 7468 |
| rs115581011 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899281 | CCCCTATTGCTGCAC[A/G]TCAGGTGTCCTCCAC | 7468 |
| rs115641423 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958146 | GGACTGTCACCAGCC[A/T]GGATCTGTGGTGCCT | 7468 |
| rs115684256 | snp | C/T | 0.0383715 | 0.133092 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869911 | TCCAGCACCATTTGT[C/T]GAAAAGACTGTCTTT | 7468 |
| rs115728315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894345 | TGCTCAGAACATAGG[A/G]TGCTCTTTTATTCAG | 7468 |
| rs115752502 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919587 | TTAATTTTACTTCCA[C/T]AGGAATTTTCCATTC | 7468 |
| rs115857579 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891474 | GCTCAGTTGGATTCA[C/T]GGAATTATCAGAGTG | 7468 |
| rs115884145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940212 | ACCTGATTCCTGTTG[A/C]TTCCAGACCTAGGCT | 7468 |
| rs115891278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963474 | TTATTTGTTAGACAT[C/T]GAAGCCCTAGGTCTG | 7468 |
| rs115892992 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927173 | GGCTGCTGGTGTGTC[C/T]TCACAACATGATGGG | 7468 |
| rs115893772 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979583 | TTGAATGAAATGCCA[A/G]TAACACGTCCACTTT | 7468 |
| rs115907720 | snp | A/C/T | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931865 | CACTAAATTTAGAGA[A/C/T]GTGTTCCTTTTAAAT | 7468 |
| rs115912214 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872198 | TGGCAGGTGGAGGCG[C/G]GGGTGAGCCGGGTGT | 7468 |
| rs115981044 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939335 | GATTTGTGCTAAACT[G/T]CTTATGGATGAAATG | 7468 |
| rs116011285 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970220 | GTAGATACCCAGGCA[A/G]AAAAACAAAACAAAA | 7468 |
| rs116022053 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896280 | CAAGCCCCAGCACCT[A/G]AACCCTGGGGTCCTG | 7468 |
| rs116056077 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899382 | GCAGCATCCATGACC[A/G]CAACCCATCAGAGGT | 7468 |
| rs116110889 | snp | C/G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981030 | GACTACCAATGCTTA[C/G/T]GTCAAAACAGCAGAA | 7468 |
| rs116150648 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905933 | GACAGAAGCTGTCTC[C/T]CCTTTGTCTGAGGAT | 7468 |
| rs116151365 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925070 | GAATTTTCTGTTATC[A/G]GAAAAGCAATGACTA | 7468 |
| rs116160053 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931232 | ACCTTACAGGGGTCC[A/G]GAGTGTGGGCAGCTC | 7468 |
| rs116176068 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919925 | TGGCGACAGAATGAG[A/G]CGCCGTCTCAAAAAA | 7468 |
| rs116177396 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932032 | CAGTGTGTGTCAGGT[A/G]TATGCAGGTTCTTGG | 7468 |
| rs116228700 | snp | A/C | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891440 | TCTCACTGCTGTCCT[A/C]GGGTTGAGACCTCCT | 7468 |
| rs116231001 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898858 | TTATAGTTGTTACAG[G/T]TGCTTCAAACTCTCC | 7468 |
| rs116232564 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911549 | CCCGAGATCGCAGTA[C/T]TGCACTCCAGCCTGG | 7468 |
| rs116233030 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896676 | CCGGCCTCCCTCCCT[C/T]CCTCCCTTCCTTCCC | 7468 |
| rs116247732 | snp | C/G | 0.0236746 | 0.106192 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870252 | GTGTCGTTCTATAGC[C/G]CGGGTAGCGCACTTT | 7468 |
| rs116267834 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963904 | TCAGGAGGCTGAGGC[A/C]GGAGGACTGCTTGAG | 7468 |
| rs116319273 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910055 | TAATATACATGCAAA[A/C]GTGAACATAACTCAT | 7468 |
| rs116331242 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966872 | ACTGAAAAGGATGGG[A/G]ACAGAGCTGTAAAGG | 7468 |
| rs116355785 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869698 | TTTGGTGATAGAGAC[A/G]AGGTCTTGCTATGTT | 7468 |
| rs116429307 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962858 | TTTTTTTAAATAAAA[G/T]AATTGTCTTGAAATA | 7468 |
| rs116458049 | snp | A/G | 0.0667028 | 0.170006 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890606 | GCACCCGGCCTATAC[A/G]AGGTTTTTTATTGAG | 7468 |
| rs116468055 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924324 | TTGGTGAGGTGCTGT[A/G]TGCTCTTGGGCCCTG | 7468 |
| rs116549916 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896083 | GTAGAGGCTCTTGGC[C/T]GGGGTCCCACAGTGT | 7468 |
| rs116557881 | snp | C/T | 0.0110088 | 0.0733705 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953217 | CAGGTGCTTTAGCAG[C/T]ATGGCTGCCTCTGAA | 7468 |
| rs116561799 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927715 | CAATGAGACTCTTAT[C/G]TCAGAAAAAAAAAAA | 7468 |
| rs116613038 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930153 | GACAGAAGCCAGCTC[A/G]CACTCCTTGGTGTGT | 7468 |
| rs116640337 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895865 | TCTGTCACCCCAGTG[A/G]CCTCTGGTGGGTGTT | 7468 |
| rs116663042 | snp | C/G | 0.0162398 | 0.0886349 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982222 | ATTTTATATGGGATT[C/G]TTTGATTTTTTTTCC | 7468 |
| rs116664822 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877852 | TCTCGGGCACCTTCT[C/G]TGACCACTGATTTAA | 7468 |
| rs116789191 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957051 | GCTGCGACTGTCGGC[A/G]AAGTCTCCTAACTGT | 7468 |
| rs116806221 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929955 | ACTTCGGTGTGTCTG[C/T]GGATCATCCTAGAGA | 7468 |
| rs116823729 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895196 | CTGTTGATGGGTTAC[A/G]TCTACCTTTTGGCTA | 7468 |
| rs116831094 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958235 | GTTCTTGGATCCGCC[C/T]TGGAGTGTGAGGCTT | 7468 |
| rs116839771 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966016 | CAAATTTCTCATCAG[C/G]AATTTTGAAGGCCTA | 7468 |
| rs116937126 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919471 | CATAATAAAGGCTGT[A/C]AAGAACTGAAGGAGT | 7468 |
| rs117060816 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886550 | TAAAAAGTAACTTGC[A/G]GCTGGGCGCGGTGAC | 7468 |
| rs117145805 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963923 | GGACTGCTTGAGCCC[A/G]GGAGTTTAAGACTGC | 7468 |
| rs117181872 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924817 | TTGTAGTCTTAGTTA[C/T]TCAGGAAGCTGAGGC | 7468 |
| rs117538303 | snp | C/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891250 | ATTCAGTGATAGCAG[C/G]GCTGAAATATATTTC | 7468 |
| rs117600071 | snp | A/C | 0.00914312 | 0.0669923 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979779 | AATATATTTTTGCTA[A/C]ACCTATTTCACAAAT | 7468 |
| rs117641566 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944498 | ATTTGACTCACTTCA[C/G]ACCATCTTCCACACA | 7468 |
| rs117660592 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977953 | CCAACATGGTGAAAC[A/C]TCATCTCTACTGAAC | 7468 |
| rs117716955 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880464 | TCTGCCTGATATTTC[C/T]TCATTCATTGAGTAT | 7468 |
| rs117770518 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962928 | TGCTCTGTCAGGGCG[C/T]ACCACCCAGGGGATA | 7468 |
| rs117862582 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881003 | TCCCTTTTAGAGGTG[C/T]ATACAGACATTTACT | 7468 |
| rs118030317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896361 | TTTCTAGACCTGGAG[A/T]TTCTCTCTATTGCTT | 7468 |
| rs118071336 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917842 | GCTAGAGTGCAGTGG[C/T]GTGGTCTCGGGTTAC | 7468 |
| rs137922428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938829 | AAAAGTGATTTCAAC[C/T]AGAAGTTTTCAGGTT | 7468 |
| rs137966515 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891601 | CTCATGCCTGTAATC[C/T]TAGCACTTTGGGAGG | 7468 |
| rs137974842 | snp | A/T | 0.000153988 | 0.00877328 | missense | WHSC1 | GRCh38.p7 | 4:1957940 | CTTTTTAGCACTGCA[A/T]GAAGCTGAAGCTCGT | 7468 |
| rs138001317 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975726 | TCCCGTTCCTGGTGG[C/T]GGCCACAGTCCTTGC | 7468 |
| rs138013159 | snp | C/T | 9.88419e-05 | 0.00702931 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951125 | ATACGAAAGTGCAGA[C/T]GAAACACAAACTGAA | 7468 |
| rs138039215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978407 | TGCCGAAACATAAAG[A/G]GACGCTAACAGGTGG | 7468 |
| rs138041764 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932191 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCAAGG | 7468 |
| rs138060967 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886317 | GCTCAGGCAATTCTC[A/G]TGCCTCAGTCTCCTG | 7468 |
| rs138089448 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971979 | GGCCGGTTCAGAAAT[A/C]AGGCAGGACGCTCAC | 7468 |
| rs138137147 | snp | C/T | 0.000194331 | 0.00985534 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901230 | TCTTGTGTCTAAGAT[C/T]TCAAGTCCTTCAGAT | 7468 |
| rs138156949 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971044 | TGCAAGGAACAAAGA[A/G]ATTCTGGAAGGTTAA | 7468 |
| rs138167863 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921838 | TCACCATTTAATAAA[C/T]GTTGTACGGAAAATA | 7468 |
| rs138182580 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921011 | CCATTGCACTCTAGT[A/C]TGGGCCACAGAGTGA | 7468 |
| rs138198831 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885832 | CAGGACAAGTTCCAG[A/G]CGCAGGAATGATATA | 7468 |
| rs138243714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905101 | CGCCATTGCACTCTA[A/G]TCTGGGCAACAACAG | 7468 |
| rs138333037 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873740 | GTAAAACATGCAAAA[C/G]TAGCTGGAATTAGGC | 7468 |
| rs138346871 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874520 | AGTGCCGAATAAATG[G/T]GTATATGGCTTAGGG | 7468 |
| rs138358803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956641 | GGGAGGCAGGAGCAA[C/T]GATGTGGCATGGCTG | 7468 |
| rs138389264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895390 | AATGAAACATTCATG[A/G]ATGTTATGTCTTAAT | 7468 |
| rs138425616 | snp | C/G | 4.95054e-05 | 0.00497496 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904353 | TTCTGCAGATCCACT[C/G]CTTCACAGCTATACC | 7468 |
| rs138431313 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945608 | ACCTGTGATGGCAGG[A/G]CTGTGAGCTGGGCTT | 7468 |
| rs138439065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960822 | ATTGCCACTTCGTGA[A/G]TACTTAATACATTTT | 7468 |
| rs138456329 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949743 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCT | 7468 |
| rs138501055 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900317 | CAGGGATGATTGGCA[A/G]GTTAAGTTATGTGTC | 7468 |
| rs138529769 | snp | C/T | 0.000165185 | 0.00908655 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955189 | GTGTGTCCGCTGCCC[C/T]GTTGCCTATCACAGC | 7468 |
| rs138581332 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891413 | GCCTGGCTCTGGGGA[A/C]TGTCCTGAATATCTC | 7468 |
| rs138599183 | snp | C/T | 0.00143218 | 0.0267215 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974865 | CTTGACCTTACAGGA[C/T]CGTATAATAGACGCT | 7468 |
| rs138665712 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888438 | AAAAAAAAAAAAAAA[-/G]ACTTTATATGCCAGA | 7468 |
| rs138680926 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979298 | GGTCGCTAGAAACTC[A/G]TCTTCGCGTTGCCCC | 7468 |
| rs138690494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922415 | AAATAACTGATATTT[C/T]AGCAGACCTCAATAA | 7468 |
| rs138694004 | snp | A/G | 0.000115381 | 0.00759455 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961091 | GGAGGAGTGCATGGC[A/G]AGAATCAAGCACGCA | 7468 |
| rs138700240 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933359 | CTTGAGGGTGACAGC[A/G]TCCTTCAGGGCAACA | 7468 |
| rs138727460 | in-del | -/GC | 0.0236746 | 0.106192 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969647 | AGGAGGCCAAGGCGC[-/GC]AGTAAGCCAAGGTCC | 7468 |
| rs138762103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965692 | GGTTTAATTGATGAC[C/T]CACAGTTCCACATAA | 7468 |
| rs138781220 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883010 | GGCCATTCTTGGGAT[C/T]GTGGGTGTGGAGAAA | 7468 |
| rs138833364 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950586 | CGCATGGTCTCCACC[C/T]CGGCGGCAGCTGGAC | 7468 |
| rs138946638 | snp | C/T | 0.0015474 | 0.0277724 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974964 | GACAGTGAATGGGGA[C/T]ACTCGTGTGGGCCTG | 7468 |
| rs138957998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944824 | TGCAAAAATTAAATG[G/T]CTTTTTTCAGCATAC | 7468 |
| rs138977345 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908176 | TAGTCTAGAACAGCA[C/T]TCCCAATCCCCAATT | 7468 |
| rs138992138 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904849 | ATATTAAGAATGTAC[A/G]GCCGGGCACGGTGGC | 7468 |
| rs139038407 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973027 | CTGGATAATTTTTTG[C/T]ATTTTTATTAGAGAC | 7468 |
| rs139057631 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961333 | CTGCGCCGGAGGGCT[A/G]GAGCTAACCACCTCT | 7468 |
| rs139098029 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908920 | CCCAAATTGTTGGGA[G/T]TACAAGTGTGAGCCA | 7468 |
| rs139111116 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938412 | TTTTCTTTTTTTTTT[C/T]TTTCTTTTTTTTTTT | 7468 |
| rs139187723 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915760 | TCCAGAAGACTCACT[A/G]GAGAGGTTTTTCCTC | 7468 |
| rs139213191 | snp | A/C | 1.69608e-05 | 0.00291206 | missense | WHSC1 | GRCh38.p7 | 4:1978817 | GCATCGGTCAGAAGC[A/C]CCAAGACTGAGAAGC | 7468 |
| rs139225905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875254 | GTGAACCACTGTGCC[C/T]GGCCAAGTTGCAGTA | 7468 |
| rs139235064 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963028 | CCTATGACATTGGAA[C/G]AGGGATTCTGAAGTG | 7468 |
| rs139266455 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897485 | GGTAGTGAGACCCTG[C/T]CTCAAGGGAAAAAAA | 7468 |
| rs139360679 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977052 | GGCCTCTACAACAGT[A/G]TCTCCCTGGCAGCCC | 7468 |
| rs139475475 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886980 | CCTCCCTTCTTCTTC[C/T]CAACATTCCCAATAT | 7468 |
| rs139492627 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883896 | CTCTTGTTCTCTGTT[C/G]ATGGTTTTCTACACA | 7468 |
| rs139523257 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981689 | GGCTGGGTCCCCTTC[A/G]CAGTGTTTGTCTGTC | 7468 |
| rs139558369 | in-del | -/CTCCCTTCCTTCCTCT/CTTCCTTCCTCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896681 | TCCCTCCCTCCCTCC[lengthTooLong]CTTCCTTCCCGAACT | 7468 |
| rs139606787 | snp | C/T | 1.64904e-05 | 0.00287139 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975385 | TTGCAGTGGATTCCT[C/T]GGGGATAGACCAAAG | 7468 |
| rs139615238 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936593 | GAATCACTTGAACCT[C/G]GGAGGCGGAGGTTGC | 7468 |
| rs139616564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961954 | TCATCTAGCAGGAAA[A/G]TCTGGCTATTTTTAA | 7468 |
| rs139637100 | snp | A/G/T | 5.12784e-05 | 0.0050633 | missense | WHSC1 | GRCh38.p7 | 4:1955328 | GTGAGCTGGTGCTTC[A/G/T]TGTGCTCCAAAGGTG | 7468 |
| rs139642094 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940485 | CAAAAACAACAAATA[A/G]CCACAGAACGTAGGT | 7468 |
| rs139642737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909584 | CGTGGAGTGGGCTGA[A/G]CATGGGTCCTGTGAA | 7468 |
| rs139693270 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941035 | TTAAGCATTTTGTGA[C/T]GTTTGGACACACTGG | 7468 |
| rs139736882 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895851 | TTCTCAAGGGTGGCT[C/G]TGTCACCCCAGTGGC | 7468 |
| rs139753036 | snp | A/C | 0.00630483 | 0.0557912 | missense | WHSC1 | GRCh38.p7 | 4:1935170 | GGGAAAAAAAGAAAC[A/C]ACACAAAGAGGATAC | 7468 |
| rs139760177 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951882 | TTACTTCCTTTGCCA[C/T]TGCTGAGGACTGGCC | 7468 |
| rs139797487 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902410 | TTTTATTTTTTGTAG[G/T]ACAGGGTCTTGCTGT | 7468 |
| rs139799356 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957407 | TCCTGCCTCAGTCTC[C/T]CAAGTAGCTGGGACC | 7468 |
| rs139862256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912770 | TCTTCCCTTGGAGCT[C/G]TCTCCTAGAATCTTC | 7468 |
| rs139881993 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917441 | ATTTCTATTATTTTT[A/T]AAAATTTTTTTGAGA | 7468 |
| rs139895251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951256 | GTCTGACTGGGGCCC[C/T]GGTACGCAGAGCGAA | 7468 |
| rs139908154 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935597 | GGGTGTGGTGGCTTA[C/T]GTCTCTAATCCCAGC | 7468 |
| rs139947244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880232 | TCTTCTCATTGAATC[C/T]TCACAGCAGGAAATT | 7468 |
| rs140040537 | snp | C/T | 0.0089484 | 0.0662882 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900852 | CATGCAGAAGTTTAA[C/T]GGCCACGACGCCCTG | 7468 |
| rs140076393 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977395 | GGGTGCAGCCACCTC[C/T]GTTACAATCTTGCAG | 7468 |
| rs140091295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896388 | GCTTTGCATTAGGCA[A/G]TGTAGCTAGACAAGG | 7468 |
| rs140096622 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981264 | GTCTCTACAATACCC[A/G]TTGATAACTCAGTGG | 7468 |
| rs140141285 | in-del | -/GG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972286 | ATATGGATGAGTGGC[-/GG]GGTACAGGCTATGTC | 7468 |
| rs140181871 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928563 | TGATGATGACACTTT[C/T]CTGGCTTCCCCGCAG | 7468 |
| rs140182983 | snp | C/G/T | 0.000512168 | 0.0159946 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938509 | AGGCCATGGAGGCAG[C/G/T]CTCCTCGCTCAAGAG | 7468 |
| rs140200637 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885123 | TTCAAAAAAAAAAAA[-/T]AAAAATAAAAAAAAT | 7468 |
| rs140212386 | snp | A/G | 0.000153988 | 0.00877328 | missense | WHSC1 | GRCh38.p7 | 4:1918346 | TGGCAGAATCCTCAG[A/G]AGTCAGTGAAGAAGC | 7468 |
| rs140217665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949177 | TTGGAGGTTTGAACT[C/T]AGAGCACGTCAAGTG | 7468 |
| rs140223844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884394 | GAGCCACCGCAGGCC[C/T]CTTTTGTTCTTTTTT | 7468 |
| rs140246901 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873395 | ACATATAAACTAATA[C/T]AACTTTTGGAGCCAT | 7468 |
| rs140318262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928448 | AATTGTGTGTGAGCA[C/T]GCGCTTTTGTGTTTT | 7468 |
| rs140337521 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978273 | CCAGAAAGATGAATA[A/C]CCAAGTTGAAAATCA | 7468 |
| rs140377762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931851 | TCACTCTATCAGTAC[A/G]CTAAATTTAGAGACG | 7468 |
| rs140401180 | snp | C/T | 1.64972e-05 | 0.00287199 | missense | WHSC1 | GRCh38.p7 | 4:1901052 | TCACCAAAACATACA[C/T]GAATGGGAAGCCTCT | 7468 |
| rs140468997 | snp | C/G | 0.000181313 | 0.00951965 | missense | WHSC1 | GRCh38.p7 | 4:1935180 | GAAACCACACAAAGA[C/G]GATACAGGACCCTAC | 7468 |
| rs140478979 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977707 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 7468 |
| rs140486025 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970304 | CAGGACCCAGTGCTC[A/G]GGACAGGGTGGGCTC | 7468 |
| rs140494040 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885597 | GTCTCAAGTGGCTGC[C/T]TGGGGCCACACATCA | 7468 |
| rs140516422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930522 | TGGGAATAAAAATGC[A/G]ACACACTAAGTTCTA | 7468 |
| rs140603753 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964502 | CACATGTTCTTGGAG[C/T]ACCTCGCACACAGCT | 7468 |
| rs140638887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913760 | CAGACATTCAGGGCC[A/G]CTACCAGTCTCCGCA | 7468 |
| rs140646464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946893 | ATGGTTACGTGTTAG[A/G]TCCACATTTGTGTTT | 7468 |
| rs140671737 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959194 | TGGCCTGGCTGGATA[C/T]GTGTCAGCTCTTGTT | 7468 |
| rs140719721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943792 | AATGGCTCTGGTTCA[A/G]TAAGCAGTCACCCAA | 7468 |
| rs140730982 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905729 | CTCCTGTCCTGTGCC[A/G]TGTGTGCTCTGCAGG | 7468 |
| rs140731423 | in-del | -/GTG | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882230 | CTGTCTCCTTGAAAT[-/GTG]GTGTGGCCTGTGATT | 7468 |
| rs140755867 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879824 | TGGGCCCATGGCACT[-/TG]TGTGTGTGTGTGTGT | 7468 |
| rs140763584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904126 | GGTCTGTGTGTATTT[C/G]GACATTGTAGCCTGG | 7468 |
| rs140806595 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907993 | CAGTTTCCTTATTGA[C/T]TCAGCACCAGCCGCA | 7468 |
| rs140831176 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903173 | GCCGGCCTCTTCAGC[C/T]TACAGGTGAGAAAAC | 7468 |
| rs140834348 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937639 | TCTGACATGCTAGGC[A/G]CTGTCCCAAGTGCAT | 7468 |
| rs140880376 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891200 | TGCCCCGCCTACGTG[A/G]AATTGTTTTATATGA | 7468 |
| rs140890804 | in-del | -/TGG | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887780 | ATGACTTTGTTTTCC[-/TGG]TGGTAAGTTTTTCTG | 7468 |
| rs140988715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925383 | GAGGTCATTTTCTTT[C/T]TCTTTCTTTTTTTTT | 7468 |
| rs141010572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881940 | CTGTGCAGAGCTTCT[C/G]TGATAGAGCAGGAAG | 7468 |
| rs141016191 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973463 | CACCGCGGCTCAGCG[C/T]GTCATGACAAAGCAT | 7468 |
| rs141052241 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923784 | CCAAAAAGCTACCCA[A/G]TGACAGACTATGGTA | 7468 |
| rs141054209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976268 | AAAGCTCACTCTAGT[C/T]GTAGTCTTTGTTCAG | 7468 |
| rs141093629 | snp | A/G | 0.00054823 | 0.0165473 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974626 | CCAGCTCCCTGTCCT[A/G]TCCTCCCCGGCGCTC | 7468 |
| rs141095288 | snp | A/G/T | 7.10941e-05 | 0.00596179 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955727 | TGAGTCCTGCCCAGC[A/G/T]GCCTTCCACCCTGAC | 7468 |
| rs141116289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877636 | TGACTCCTGCCTGTT[C/T]TGGGAGGCTCTTGTC | 7468 |
| rs141132577 | snp | A/G | 0.000263617 | 0.0114778 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935241 | GAAAAGACTCAGGAC[A/G]GACAAGCACAGTCTT | 7468 |
| rs141155485 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899670 | CTAGCTGTGTTTTGG[A/G]GCTCTGGCCCCTTCA | 7468 |
| rs141176487 | in-del | -/GAC | 0.0162398 | 0.0886349 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907554 | TAAAACAGCACAGCA[-/GAC]ACCTATCCCCTCATC | 7468 |
| rs141181603 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886081 | CTTATCTTTTCCTTT[A/G]CGAAACTAAAGCGCG | 7468 |
| rs141191479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971642 | GAGCCAGGGCGTGGA[C/G]CTGTATGTGAACATG | 7468 |
| rs141196625 | snp | C/G/T | 0.0393377 | 0.135698 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972818 | GCACGGAAGATTCCA[C/G/T]TGGGAGCTGGGAAGC | 7468 |
| rs141228128 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973926 | TGCTGGGTGGAGATG[A/T]TGTCTCCAGTTCCTG | 7468 |
| rs141283529 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881326 | GGAGTGCAGTGGCGC[G/T]ATCTCGGCTCACTGC | 7468 |
| rs141298023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943188 | GCATGGTAAGGAAAA[A/G]GCTTACTTGCCCTTC | 7468 |
| rs141332896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967107 | ACATTATTACTGCTT[C/T]TACAGAAATAAAAAA | 7468 |
| rs141340057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947359 | GGGGCTATGTGGCTA[C/T]GGCTACACAAAAGCC | 7468 |
| rs141340229 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1893956 | GATTGATTGACAGAC[A/T]GTCTTGCTCTGTAGC | 7468 |
| rs141397822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878902 | CGGACTGGGCCATAG[C/T]GTGAGAGTGGTGCAG | 7468 |
| rs141429899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898213 | TGCCTCAGCCTCCTG[A/G]GTAGCAGGGACTACA | 7468 |
| rs141506731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955482 | TAATAGTATATCACA[A/G]TAGCTCTAAATTAAT | 7468 |
| rs141528201 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904929 | TGAGGTCAGGAGTTC[A/G]AGACTAGCCTGACCA | 7468 |
| rs141584086 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976795 | GCAGGCACATCAGGC[A/G]CTCATGCAGCGAAGG | 7468 |
| rs141672511 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927547 | ACATGGTGAAACCCC[C/T]ATCTCTACTAAAAAT | 7468 |
| rs141714369 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919705 | TTGGGAAGCTGAGGC[A/G]GGTGGATCATGAGGT | 7468 |
| rs141720085 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883324 | TGATACCCCTCCCCC[C/T]ATTTAAAAGTGTACC | 7468 |
| rs141750228 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878012 | CCAGACTGGGTGGCA[A/G]TAAGACTCTGTCCCA | 7468 |
| rs141752298 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924228 | TGTGTGTACAGCCAC[C/T]GTTTCAGGCATGTTG | 7468 |
| rs141757418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880307 | TATGTGATGAAGTTA[A/G]AACTCCTGCAGGGCC | 7468 |
| rs141824804 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916776 | TAACAGGCTCAGACA[A/G]CACCAAGGGAAACAA | 7468 |
| rs141827113 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883185 | TACTGTCCAGATAGC[A/T]TTCTTTCTGTGTGCA | 7468 |
| rs141927913 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908711 | TGTGGAAAGGCACAG[G/T]TCCCCATTGTCACTA | 7468 |
| rs141972110 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981003 | CCAAAAGATCCCTTC[C/T]GGCAGGTAAGGGACT | 7468 |
| rs142000931 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935021 | CTGGAAATCAGCAGG[G/T]TTACAGGAAACCCAT | 7468 |
| rs142004038 | snp | C/T | 0.000115484 | 0.00759794 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961115 | GCACGCACACGAGAA[C/T]GACATCACCCACTTC | 7468 |
| rs142034802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881212 | CCTCCTGCGTAGCTG[A/G]GACACAGGCGTGTGC | 7468 |
| rs142039924 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963916 | GGCAGGAGGACTGCT[G/T]GAGCCCAGGAGTTTA | 7468 |
| rs142054662 | snp | A/C/G | 0.000344268 | 0.0131158 | missense | WHSC1 | GRCh38.p7 | 4:1978838 | ACTGAGAAGCCCCCC[A/C/G]CAGAGCCAGGGAAGC | 7468 |
| rs142100377 | snp | C/T | 0.000578422 | 0.0169964 | missense | WHSC1 | GRCh38.p7 | 4:1959501 | GGGAAAGTCCAGATC[C/T]ACACAGCGGATATTT | 7468 |
| rs142143853 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958232 | GGGGTTCTTGGATCC[A/G]CCTTGGAGTGTGAGG | 7468 |
| rs142189381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940014 | TCTGTGTACATGTAC[A/T]GATATACTTCAGTCT | 7468 |
| rs142191128 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906650 | TTTACTTCTCTCTCT[C/G]TCTCTTTTTTTTTTT | 7468 |
| rs142228365 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944999 | CACAACCTTTCATGT[C/T]GTGAAAGGCAGAGGG | 7468 |
| rs142236442 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928204 | CATGTGTCCAGCTTG[-/T]TTTTTGATATGTTAA | 7468 |
| rs142248724 | in-del | -/TCC | 0.0667028 | 0.170006 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893657 | CCCAGGCTCAACTGA[-/TCC]TCCTGCCACAGCCTC | 7468 |
| rs142278631 | snp | A/G | 6.60099e-05 | 0.00574461 | missense | WHSC1 | GRCh38.p7 | 4:1978742 | GAGCACCAGGACGGG[A/G]CAGCCTTCAGCTGCA | 7468 |
| rs142297375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946433 | CCACCACACCTGGCT[A/G]TTTTTTTTTGTATTT | 7468 |
| rs142379152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885341 | CTCAGACACCTGCTT[A/G]TGGATCAGTGGAGCA | 7468 |
| rs142409548 | snp | A/G | 0.000561918 | 0.0167524 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955285 | CTTCACTGCTCGGAA[A/G]GGGAAGCGACACCAC | 7468 |
| rs142446400 | snp | C/T | 0.0681886 | 0.171594 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891739 | GTCGGCACCTGTAGT[C/T]CCAGCTACTCGGCAG | 7468 |
| rs142488159 | snp | A/G | 0.021333 | 0.101051 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918017 | AACTCCTGGCCTCAA[A/G]TGATCCATCTGCCTT | 7468 |
| rs142506599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965533 | GAAGCTCAATAAACT[C/G]CAGATGATCAAACTT | 7468 |
| rs142512153 | snp | A/G | 5.32543e-05 | 0.00515987 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901233 | TGTGTCTAAGATCTC[A/G]AGTCCTTCAGATAAA | 7468 |
| rs142535205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876624 | TGAGTCCAGGACTTT[C/G]AGGCTGCAGTGAGCT | 7468 |
| rs142545290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968687 | AAGTGGTTTAAATGT[A/G]TAAGTTAAGACTAAG | 7468 |
| rs142545380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914446 | TTCTCCCGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 7468 |
| rs142605460 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917296 | ATACACATATATGTA[C/T]GTATATATGTGTATA | 7468 |
| rs142634124 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982117 | TTGCCAGTTGGGGGA[A/G]AATAGCATTTAAAAT | 7468 |
| rs142639234 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872161 | GACGCTCCCCCGGGA[A/G]GCCGGGCCGCGGTCC | 7468 |
| rs142642769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951913 | TCTTTCTGTAACAGT[C/T]ATCTGGTTTTAATCT | 7468 |
| rs142719686 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934439 | CAGAGGTTGCAGTGA[A/G]CTGAGATTGTGCCAT | 7468 |
| rs142740424 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937962 | AAATTGGAAATCCTC[A/T]GTATAGTGATACTAG | 7468 |
| rs142741742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886882 | ATTTTAGAACTTCCA[A/G]ATTGATATATGTTCA | 7468 |
| rs142788221 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891590 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 7468 |
| rs142797858 | in-del | -/GTT | 0.067446 | 0.170804 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934013 | TTTAAAAAGTAGCAA[-/GTT]GTTTTTTTTTTTAAG | 7468 |
| rs142836236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901871 | CACACTGAACACAAG[C/T]GAATGAGTGTTTCCT | 7468 |
| rs142882250 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973803 | ACACGTGGTTTTGTT[C/T]GAACACGTGACTGTT | 7468 |
| rs142903185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924884 | GTGAGCCATCATTGC[G/T]CCACTGCACTCCAGT | 7468 |
| rs142907708 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946096 | ATCTATAAATAGGGT[A/C]ATTGCTGAGGTGTGC | 7468 |
| rs142995364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896126 | AGCTGGGATTCTAGT[C/T]CAGACAGCAGCTCCA | 7468 |
| rs142999179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950314 | AGAGATACAACCTGC[A/G]AGCAATTCCACTCGC | 7468 |
| rs143035889 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900510 | ATTATAAAAACATCA[A/T]AAATTGCTTACAAAG | 7468 |
| rs143043790 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909268 | TTTCCCACCACCCCC[C/G]CCAACCCTAGCATCA | 7468 |
| rs143044443 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948002 | TGTTCACTAGGTTCC[A/G]TTATGTTTGGTAATA | 7468 |
| rs143090219 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899497 | AGAACCGCTGTTCTA[C/G]TCCACGGGCATCTCT | 7468 |
| rs143124937 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935247 | ACTCAGGACGGACAA[A/G]CACAGTCTTCGGAAG | 7468 |
| rs143171304 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874399 | GCTTTTTAATGGCCA[C/T]TTGTGACCTTTCTCC | 7468 |
| rs143198454 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977819 | ACCAAACAAACAAAA[A/C]ACAAAACTATAAAAA | 7468 |
| rs143218504 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913250 | GTGCCTGGGAAGGCA[C/T]CTGTTACTTAGCCGA | 7468 |
| rs143253061 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878422 | CAAAAAAACTTTTTT[A/C/T]AATTATTCTGTTGCT | 7468 |
| rs143256354 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917761 | TTTCTAAAATTATGT[A/G]AAAATGTAAAAGTAT | 7468 |
| rs143346723 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875480 | AGACAGGATTTCACC[A/G]TGTTGCCCAGGCTGG | 7468 |
| rs143355773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874148 | CTACGTGTTTGGTTT[C/T]GCCTTTTTGTTTTTG | 7468 |
| rs143360610 | snp | A/G | 0.000659565 | 0.0181479 | missense | WHSC1 | GRCh38.p7 | 4:1955241 | GGATGCTCAGTGATC[A/G]CCTCCAACAGCATCA | 7468 |
| rs143374402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973263 | GATGAAAACTGGCCC[A/G]ATAAGAAGGAAGTGG | 7468 |
| rs143388708 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951184 | GAGGAGTGACTGCCA[A/G]AAAGGAGTATGTGTG | 7468 |
| rs143425918 | snp | A/G | 0.00146352 | 0.0270114 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918203 | CATTGTTCAAGCAGA[A/G]GAAGCTGCAAGCATG | 7468 |
| rs143428268 | snp | C/T | 0.0667028 | 0.170006 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891632 | CTGAGGCGGGCAGTT[C/T]ACGAGGTGAGGAGAT | 7468 |
| rs143459231 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903902 | ACCACGCCCGGCTAA[G/T]TTTTTGTATTTTTAG | 7468 |
| rs143464964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975764 | TGGCTTGTAGCAGCA[C/T]CGCCCAACCATTCTC | 7468 |
| rs143506366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978541 | GCACTATTTTGTGTT[C/T]ATTTGACCTGACAGT | 7468 |
| rs143523467 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895287 | CTTTTGGGTAGACAG[A/T]CTGTTTTTCACCCTG | 7468 |
| rs143614523 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937138 | CTCACTGCAACCTCC[A/G]CCTCCTCGATTCAAG | 7468 |
| rs143621443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977417 | ATCTTGCAGTGTGTC[A/G]CCATGAGGCTCTTGA | 7468 |
| rs143637491 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892509 | TTATTTTAAAAAACA[A/G]CAATGTGATGCTTAA | 7468 |
| rs143714734 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981298 | CAGGCTTTGGGGTAG[C/T]GGCCCTGAGCTTGCA | 7468 |
| rs143779528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908557 | AGGAGATTCAGATAA[C/T]CTTAAAAGAAAAGGG | 7468 |
| rs143787373 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938416 | CTTTTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 7468 |
| rs143859686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923473 | TGCTCAACTGCGGCC[A/G]TGCCCAGGAAGCTGT | 7468 |
| rs143882726 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896291 | CCTAAACCCTGGGGT[-/C]CCTGCCATGGGCAGC | 7468 |
| rs143903110 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960915 | TGTACACGCCCTCCA[C/T]GGAGGTATGCTGATG | 7468 |
| rs144003128 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958794 | GTATGAAATGTTTAG[A/G]TTCTTGGGGAATATT | 7468 |
| rs144026220 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886485 | GTTCTGGGATTACGG[A/G]CTTGAGCCACTGTGC | 7468 |
| rs144038154 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972355 | CCCCAGTGCAAGCTC[A/G]TTGTAGGTGCGATAA | 7468 |
| rs144049254 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907983 | AGAACAAGGACAGTT[A/T]CCTTATTGACTCAGC | 7468 |
| rs144051014 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963203 | GGCAAGATGGGAAGC[A/G]GGTCCATAAGGGCGA | 7468 |
| rs144073441 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910673 | TTGCAGGTAATCTGG[C/G]TTTCTCGTGTCTTGT | 7468 |
| rs144077075 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875388 | CTGGGCTCAATCGAT[C/T]CTCCTACCTCAGCCT | 7468 |
| rs144110920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958112 | GTTCTTAGGCACACC[C/T]AGGCTATGGCTGGGG | 7468 |
| rs144151161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928451 | TGTGTGTGAGCATGC[A/G]CTTTTGTGTTTTTAG | 7468 |
| rs144185132 | snp | C/T | 0.000120976 | 0.00777648 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955333 | CTGGTGCTTCGTGTG[C/T]TCCAAAGGTGAGGGG | 7468 |
| rs144205141 | snp | A/G | 8.23771e-05 | 0.0064173 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935196 | GATACAGGACCCTAC[A/G]GAAGATGCTGAAGCT | 7468 |
| rs144291231 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946112 | ATTGCTGAGGTGTGC[A/G]GTTTATCTTTGAGAT | 7468 |
| rs144308486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940578 | GCTTTGGAGTTTTAA[C/T]TTCTTGTTATTTGGT | 7468 |
| rs144310431 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889787 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 7468 |
| rs144327097 | snp | C/T | 3.6537e-05 | 0.00427401 | missense | WHSC1 | GRCh38.p7 | 4:1976515 | AAAAGGGCAAAAAGA[C/T]CAAGAAGAAAACGAG | 7468 |
| rs144335923 | snp | C/T | 0.000313312 | 0.0125123 | missense | WHSC1 | GRCh38.p7 | 4:1955236 | CAGCAGGATGCTCAG[C/T]GATCGCCTCCAACAG | 7468 |
| rs144351518 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891924 | TCACCAGAAATGCAC[A/G]CTAGGGCTTACCCAG | 7468 |
| rs144394391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939334 | AGATTTGTGCTAAAC[C/T]TCTTATGGATGAAAT | 7468 |
| rs144431814 | snp | A/T | 0.000891177 | 0.0210901 | missense | WHSC1 | GRCh38.p7 | 4:1916994 | TTGAAAAATTATGCC[A/T]GGAAAGTGCCAAGCA | 7468 |
| rs144431902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968372 | CATTGAACACTAATG[A/G]TCACAGGGAGCACCG | 7468 |
| rs144443308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942009 | GACACACACCCATTG[A/G]GTCACACCCCCTTTG | 7468 |
| rs144517100 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942024 | GGTCACACCCCCTTT[-/G]CATGTTTGTATTTCC | 7468 |
| rs144532092 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946923 | TTTTTCTAGCCTACC[C/T]ATAGTTGTTGGCCTT | 7468 |
| rs144545468 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926734 | CCTCGGCCTCCCTAA[A/G]TGCTGGGATTATAGG | 7468 |
| rs144570751 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905849 | CTTTCCAAGGGGTTG[C/T]GGGAACCCCAGGGTG | 7468 |
| rs144573851 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908018 | GCCGCATTTCGGGAA[A/G]CATCACATCAGTAAC | 7468 |
| rs144581181 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910017 | TATCTTAGTAATATA[C/T]TTAAATTTTGAAAAC | 7468 |
| rs144608795 | snp | C/G | 0.0314385 | 0.121371 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869996 | TCCGGGTTCTCTATT[C/G]TGTTCATGGATCTAT | 7468 |
| rs144714547 | snp | C/T | 0.0001156 | 0.00760176 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951076 | TTCATCTCTAGGTCT[C/T]GGACAGCCCGGGAGA | 7468 |
| rs144736196 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901721 | CTGTGCAGAGGTGCT[C/T]CCGCTGTCCTTACCC | 7468 |
| rs144811315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969864 | ATAGCCAGGCAGAAA[C/G]GAGAGCTAGGATTGG | 7468 |
| rs144841368 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895717 | GGGAGAGGGGGGCTC[C/T]CCATGAGCAGTTCTC | 7468 |
| rs144845434 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979531 | GGCAGCAATGGTGTT[G/T]TAAGATTTCCTCCCG | 7468 |
| rs144850325 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973638 | TATGTAGAAAGGACA[C/G]GGGGCCAGCGGTCCC | 7468 |
| rs144904997 | in-del | -/GT | 0.119281 | 0.213102 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945398 | GCCCATGGTGTGTGT[-/GT]CCAGAGGTGTGTGTG | 7468 |
| rs144907724 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926404 | GTGATCCGCCTGCCT[C/T]AGCCTCCCAAAGTGC | 7468 |
| rs144929400 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880832 | AATTTTTATTGTAGG[A/G]CTTATCTGTGTTTGT | 7468 |
| rs144940739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923952 | TATCCCTTTCTCTGC[A/G]TCCATCTAAAAAGTG | 7468 |
| rs144970629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947877 | CTCAATGTGTATGAC[A/G]CCACTCTGAAGAGTA | 7468 |
| rs145001071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887107 | GTTAGCTTGTTCCTC[C/T]TGCTCCATGTGATGC | 7468 |
| rs145132867 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941822 | CAAATAAACTTGTCT[A/G]TTATATATTAACGCG | 7468 |
| rs145175247 | snp | A/C | 0.000593598 | 0.0172176 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904196 | TGTGTTAGTGTTTGT[A/C]TTCTGTTGTTCATTT | 7468 |
| rs145196171 | snp | C/G | 0.0126979 | 0.078662 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947376 | GCTACACAAAAGCCT[C/G]TGCAGGTTAGAAGAC | 7468 |
| rs145231871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954231 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 7468 |
| rs145232242 | snp | G/T | 1.64909e-05 | 0.00287144 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900867 | CGGCCACGACGCCCT[G/T]CCCTTTATTCCAGCC | 7468 |
| rs145285460 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977355 | ATGACTCTGGCGGTG[C/T]GCAGACATCATGGCT | 7468 |
| rs145317342 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878462 | TCCACATCTGCCTTA[A/G]ATTTTCTCCATAGCA | 7468 |
| rs145326480 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951580 | GCTTCACTGATGACA[G/T]GCACACTGGACAGGC | 7468 |
| rs145327085 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928950 | CTGCTGGGTTGGGAG[A/G]GGTGTGGCAGGAGTA | 7468 |
| rs145495969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917864 | TCGGGTTACTGCATC[C/T]GCTGCCTCCCAGTTC | 7468 |
| rs145534143 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903500 | GGATGGTTCATGTTG[A/G]TGACACATGGGCTGC | 7468 |
| rs145556817 | snp | C/T | 3.29832e-05 | 0.00406085 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900855 | GCAGAAGTTTAACGG[C/T]CACGACGCCCTGCCC | 7468 |
| rs145564664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971895 | CAAGAAACCAGGACT[A/G]CAAGTATGCTTAGCT | 7468 |
| rs145579279 | in-del | -/CGTACATT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966372 | CATGATTGAAGAGAT[-/CGTACATT]AGGGCTGGGCATGGT | 7468 |
| rs145583201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886083 | TATCTTTTCCTTTAC[G/T]AAACTAAAGCGCGTC | 7468 |
| rs145587890 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964627 | CAGACAAAGAGGTGC[A/G]CTGCGCTGCCGTTGT | 7468 |
| rs145603828 | snp | A/G | 0.000164938 | 0.00907973 | missense | WHSC1 | GRCh38.p7 | 4:1901099 | TGTGGTGACAGTGCT[A/G]CTGATGTGTCTCAGT | 7468 |
| rs145618296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931000 | TTCTGGCCTGTGGCT[C/T]CCTTGCTCTCCTACC | 7468 |
| rs145631870 | snp | C/T | 1.65762e-05 | 0.00287886 | missense | WHSC1 | GRCh38.p7 | 4:1956024 | CCAAAAATGTTCCCC[C/T]AAATATTCAGAAAAT | 7468 |
| rs145647388 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884678 | ATTATAGGCGTGAGC[C/T]ACTGGGCCCAGCCTC | 7468 |
| rs145663906 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885605 | TGGCTGCTTGGGGCC[A/T]CACATCATGCTGGAG | 7468 |
| rs145672223 | snp | C/G | 0.0126979 | 0.078662 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981826 | GCCAAATATCTTGAT[C/G]CTATGAGTGTAGTTG | 7468 |
| rs145697322 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892672 | GCCTCGGGTTTGAGC[A/G]ATTCTCCTGCCTCAG | 7468 |
| rs145704598 | snp | A/C | 0.000148496 | 0.00861546 | missense | WHSC1 | GRCh38.p7 | 4:1935173 | AAAAAAAGAAACCAC[A/C]CAAAGAGGATACAGG | 7468 |
| rs145743173 | snp | C/T | 0.000709425 | 0.0188204 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961055 | ATTTGTTAACGAGTA[C/T]GTTGGGGAGCTGATC | 7468 |
| rs145841923 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959248 | AAGATAAAATAATGT[A/G]AGGGGGCGTTGTGTT | 7468 |
| rs145873307 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982687 | GGGTCCCCGGAGCAG[G/T]GAGGACAAGCTGGCC | 7468 |
| rs145873338 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933116 | TCACGAGGGCTGCTT[A/G]CCTGGCCCCCATCAC | 7468 |
| rs145895982 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949451 | GTCACCAGTCAGAGG[C/T]GACGGAAGCCCTTGG | 7468 |
| rs145928508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937782 | TCATTCCCTGGGCAG[C/T]GCTGCTCTAGTGCTA | 7468 |
| rs145961168 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963250 | AGCGCCTCTAGGACC[A/C]TGGCGTGTAGAGCAG | 7468 |
| rs145972570 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967596 | AAAAAAAAAAAAGAT[A/G]TTTCCAACTTAACAG | 7468 |
| rs145999441 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917330 | ACACACAGACAGAGG[G/T]ATTAATGTAATGTGA | 7468 |
| rs146010988 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922082 | GAACCTGGAGGCAGA[A/G]GTTGCCGTGAGCTGA | 7468 |
| rs146059943 | snp | A/G | 5.10174e-05 | 0.00505035 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978648 | TGCAGGGAAGTGGGA[A/G]TGTCCTTGGCATCAT | 7468 |
| rs146115430 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981246 | GTAACACTAACTTTG[A/C]ATGTCTCTACAATAC | 7468 |
| rs146121526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896214 | CTCTGTGCAGGCAGC[C/T]CAGTCAGGCCCAAGC | 7468 |
| rs146133441 | snp | A/C | 3.65237e-05 | 0.00427323 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900620 | TTCTTTTTTTTAATA[A/C]CATAGTGTTCTAAGA | 7468 |
| rs146198922 | in-del | -/AA | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956957 | ATTCAGAGATCTCAT[-/AA]AGAATGGGTAGGCAT | 7468 |
| rs146240684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880546 | TTATAGGCCTGTAAT[A/G]GGATGAAATGGGGAG | 7468 |
| rs146252630 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883191 | CCAGATAGCATTCTT[C/T]CTGTGTGCATTTACA | 7468 |
| rs146318719 | snp | A/G | 3.33333e-05 | 0.00408235 | missense | WHSC1 | GRCh38.p7 | 4:1955307 | CGACACCACGCCCAC[A/G]TCAACGTGAGCTGGT | 7468 |
| rs146325430 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981519 | GCATCTGCACCTAAA[A/C]CCATACCCACCCGTG | 7468 |
| rs146357695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940182 | GGGTGGGGTGGAAGG[A/C]GACTCACACACCACA | 7468 |
| rs146383153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945041 | GATGTGCAGAGTCCT[C/T]GGACAGGAGTCGGGG | 7468 |
| rs146445929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907986 | ACAAGGACAGTTTCC[C/T]TATTGACTCAGCACC | 7468 |
| rs146473947 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961213 | AGCCCTGATGGTCAC[C/T]TGTAGAACTGGACTT | 7468 |
| rs146509878 | snp | C/T | 0.000395407 | 0.0140551 | missense | WHSC1 | GRCh38.p7 | 4:1935240 | GGAAAAGACTCAGGA[C/T]GGACAAGCACAGTCT | 7468 |
| rs146531559 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974303 | GTAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 7468 |
| rs146541406 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937096 | TCACTTCGTCACCCA[A/G]GCTGGAGTGCAGTGG | 7468 |
| rs146556261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908772 | TGTCCCAACAGTGTA[A/G]CTTTTGTTGTTGTTG | 7468 |
| rs146558233 | snp | A/C | 5.4749e-05 | 0.00523178 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955718 | TCTGTGCTGTGAGTC[A/C]TGCCCAGCGGCCTTC | 7468 |
| rs146568854 | snp | C/T | 0.067446 | 0.170804 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890596 | GTGAGTCACCGCACC[C/T]GGCCTATACAAGGTT | 7468 |
| rs146578985 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892374 | CCCTCATGTTGGAGA[C/T]CTCCCAAGGTCCATG | 7468 |
| rs146680725 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953879 | TCACTGCATCCTTGA[C/G]CTCCTGGGCTCAAGC | 7468 |
| rs146685572 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873289 | GTCTGGCCTCTGATT[A/G]TAACAGTAAAGATTT | 7468 |
| rs146706930 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958347 | CACCTGCACCAGGCT[G/T]TTGCCAAGTGCTGGG | 7468 |
| rs146743725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915593 | ATTCATACTGGATGC[C/T]TCCCTGGGTCCAGGG | 7468 |
| rs146770265 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931086 | CACAAGAAGGAAGGG[A/G]AGGGAAGGTCGTCTC | 7468 |
| rs146793460 | in-del | -/ATATATA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878245 | TATATATATATATAT[-/ATATATA]TTTTTTTTTTTTTTT | 7468 |
| rs146808689 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930519 | ATGTGGGAATAAAAA[C/T]GCGACACACTAAGTT | 7468 |
| rs146819927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936076 | GAATACTAAACAGGC[C/T]GTGCAGGAAAAGTGC | 7468 |
| rs146822227 | snp | A/G | 1.69358e-05 | 0.00290992 | missense | WHSC1 | GRCh38.p7 | 4:1918562 | CAGTCTCCATGCCAC[A/G]AAGCAGGAAGGGAGA | 7468 |
| rs146940201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938301 | AAGAAGTTTCTGCCA[C/T]GAAACTTTTCAGCAA | 7468 |
| rs146963815 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943316 | ACGTTTCTGACTAAT[A/G]TTTTGTTGTAAACCA | 7468 |
| rs146973082 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894334 | TTCATTTATTTTGCT[C/T]AGAACATAGGGTGCT | 7468 |
| rs146996262 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898816 | ACTCCCCTCTGAGAC[A/T]CTCTCCTTGAGATTT | 7468 |
| rs147086551 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960296 | TTTATGAAATGGAAG[A/T]TCTGTGAAGTGACCC | 7468 |
| rs147100991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881691 | TATGAGCCACCCCTC[C/T]GAGCCCTGGTTCTAA | 7468 |
| rs147134174 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976249 | GTCATTGCAGGCTTC[C/T]GACAAAGCTCACTCT | 7468 |
| rs147143904 | snp | A/G | 0.00018872 | 0.00971207 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953520 | AAACCCAAGGCCGTC[A/G]AAAGGTACAGGTGCA | 7468 |
| rs147157320 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927638 | GTGGGAGAATCGCTT[G/T]AACCCAGGAGGCAGA | 7468 |
| rs147221143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905854 | CAAGGGGTTGCGGGA[A/G]CCCCAGGGTGTACCC | 7468 |
| rs147254888 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905650 | GTAGATGTTAGAGGG[C/G]CAGGCTGAGGACGAA | 7468 |
| rs147326811 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887209 | AGTGTGGTCTATCCT[A/G]TGAGGCTGCTTGGGC | 7468 |
| rs147336225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973438 | GTGTGCATGCCAACG[C/T]GCACATCAGCACCGC | 7468 |
| rs147351783 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934567 | TAAATTATAATTATA[A/G]GGCCAGGCGCGGTGG | 7468 |
| rs147361791 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886916 | CTATCTGTGGAAGAT[A/G]ATGGAAGATTTAGCT | 7468 |
| rs147385067 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891593 | CACGGTGGCTCATGC[C/T]TGTAATCCTAGCACT | 7468 |
| rs147409255 | in-del | -/TGTT | 0.0551013 | 0.156571 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981851 | TAGTTGATGACTGTT[-/TGTT]AGTCAGTAGAGTAAA | 7468 |