SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs147434468 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951874 | TGATCCTGTTACTTC[C/T]TTTGCCATTGCTGAG | 7468 |
rs147456465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909369 | GTTGTGTTCATTGCT[C/G]TGGGAGACAGAGTTT | 7468 |
rs147488709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874400 | CTTTTTAATGGCCAC[C/T]TGTGACCTTTCTCCC | 7468 |
rs147523648 | snp | C/G | 0.000198633 | 0.00996378 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918260 | CACCTTTCTCTATGT[C/G]GGGGACCAGCTTCAT | 7468 |
rs147538312 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928513 | CGTGAAGCTCGGAGA[C/T]GTTAATGAGGAGTCA | 7468 |
rs147609440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899366 | CGTTGCAGGAGATGC[A/G]GCAGCATCCATGACC | 7468 |
rs147618724 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982281 | GTGGCACTGATGCCT[C/T]CGATGGGTGGGGCTC | 7468 |
rs147624398 | snp | A/C/G/T | 0.00101098 | 0.022463 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978837 | GACTGAGAAGCCCCC[A/C/G/T]CCAGAGCCAGGGAAG | 7468 |
rs147633645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902827 | TCTTCCTCTGGAGAG[A/T]GGGGTCAATAAATGT | 7468 |
rs147732537 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968655 | AAAATCAAAATGTCA[A/G]TAATCACAATATATG | 7468 |
rs147770113 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884387 | CAAGTGTGAGCCACC[A/G]CAGGCCCCTTTTGTT | 7468 |
rs147820133 | snp | A/G | 0.00445058 | 0.0469625 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942322 | ATTCTTATTTTTTTC[A/G]CCTTCACTGGTAACA | 7468 |
rs147843030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947119 | GTCCTCAAGTCCTTC[A/G]CAGACAGTGCACAGC | 7468 |
rs147926959 | snp | C/T | 0.00013188 | 0.00811929 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900780 | CTGCGAGGTGAACCG[C/T]GAGTGTTCTGTGTTC | 7468 |
rs147948605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877672 | CATCGTCACCCACTC[C/G]CATTCTCATTCTGTT | 7468 |
rs147949167 | snp | A/C/G | 0.00716904 | 0.0595202 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923993 | GCTGTGAAGGTATGT[A/C/G]CCTCTCTCCAGGAGC | 7468 |
rs147996011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943767 | GATGGGGAAAAAAAG[A/G]TGGTATAAAAATGGC | 7468 |
rs148014395 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926829 | ATTTTTACACATCCA[G/T]TAGATTGGAACCAGT | 7468 |
rs148029923 | in-del | -/C/CC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924369 | GGTGTCGGGTGGGAA[-/C/CC]CCGCCCCGTCAGCCA | 7468 |
rs148070365 | snp | C/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891116 | CCAGGCTGATGTCGA[C/G]TTCTTGGGCTCAAGC | 7468 |
rs148090826 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916372 | TGTTTTTGAGACAGG[G/T]TCTAGCTCTGTCACC | 7468 |
rs148136310 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908676 | CCCACCCCTGGTAGG[C/T]GATGACCACCAGAGC | 7468 |
rs148164552 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980431 | CTTTTCTTAAAATAA[C/G]CTAAGGGGGACACAT | 7468 |
rs148207579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899660 | TTTCTTATTCCTAGC[C/T]GTGTTTTGGGGCTCT | 7468 |
rs148228020 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972531 | GGCATTCCTGTGACT[C/T]CAGCGGGGCCCAAAC | 7468 |
rs148231977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886659 | ACGTGGTGGAACCCC[A/G]TCTCTACTAAAATAC | 7468 |
rs148254848 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938507 | CAAGGCCATGGAGGC[A/G]GCCTCCTCGCTCAAG | 7468 |
rs148279921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966832 | GGCACTCAATACATA[A/C]AGATGTGATTTTGTG | 7468 |
rs148295638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878833 | CCAATGCACAGGAGG[C/T]AAGGCTGGGAAGGTG | 7468 |
rs148346589 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874313 | CATGTCCTGACTCCA[C/G]GCCTTTGTGTGGGCT | 7468 |
rs148355229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955417 | GGCAGGCTCATTCCT[C/T]GTCTGCGCTGTGTTC | 7468 |
rs148409106 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917865 | CGGGTTACTGCATCC[A/G]CTGCCTCCCAGTTCA | 7468 |
rs148459472 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883282 | ACTTCCTTAGCTCAA[A/G]TAACAGTTTCTCAAT | 7468 |
rs148460731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910369 | TAGCTGGCACTACAG[A/G]CATGTGTCACCACAC | 7468 |
rs148470441 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870039 | CCACCAGTACCACAA[C/T]GTCTCAATTACTGTA | 7468 |
rs148524282 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901798 | AGATGGCCTGCCTCC[C/G]TGAGGCCTAGGGATG | 7468 |
rs148551012 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973796 | TGTTCACACACGTGG[C/T]TTTGTTTGAACACGT | 7468 |
rs148595382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968401 | CGGGAGCGTGGTGAC[G/T]CCAGGGTGAGCTGCT | 7468 |
rs148612657 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963868 | AGAAAAAAAATTAGC[C/T]GTGCCTGTGATTCCA | 7468 |
rs148616809 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881204 | CACCTCAGCCTCCTG[C/T]GTAGCTGGGACACAG | 7468 |
rs148688095 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906455 | CATGTTGCCCAGTTG[A/G]TCTCAAACTCCTGGG | 7468 |
rs148740968 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946355 | TCACTGCAACCTCCG[C/T]CTCCTTGGTTCCAGC | 7468 |
rs148786950 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939418 | TATGGATAGAGCCAC[A/G]CTGGCCCCAGGTTGA | 7468 |
rs148848918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903727 | TAGCTGAGAGTGAGA[C/G]AGAAATTTTTTTTTT | 7468 |
rs148888459 | in-del | -/T | 0.0777841 | 0.181223 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880354 | ACCCTGGGAACTTAC[-/T]TTGTTTTGCCTCTTG | 7468 |
rs148896652 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982004 | GGTCAGATTCCTTTT[A/G]GGAATACTGGGTGCT | 7468 |
rs148963789 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889753 | CTCAGGTGATACACC[C/T]GCCTTGACCTCCCAA | 7468 |
rs148984106 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959994 | GCTTCCCAAGCAGCT[A/G]GGACTACAGGCGTGT | 7468 |
rs149058952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947909 | GTGAGCGCTTTGCAG[A/T]CACAGAAGGTGGCAT | 7468 |
rs149110753 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941941 | GTTGACTGCTGGGCC[C/T]GATTCTGATATGAGT | 7468 |
rs149121499 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893094 | TCCGCATCCCCAGGT[C/T]TGACATCTCTAACTC | 7468 |
rs149128516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937116 | GAGTGCAGTGGTGCA[A/G]TCTTCACTCACTGCA | 7468 |
rs149141253 | snp | A/G/T | 0.0134935 | 0.0810909 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921018 | ACTCTAGTCTGGGCC[A/G/T]CAGAGTGAGACCCTG | 7468 |
rs149163689 | in-del | -/AT | 0.0193772 | 0.0965046 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916149 | CTCTAGCACTGTGAG[-/AT]AGGGGGGTAGCTAGC | 7468 |
rs149198168 | snp | A/T | 0.0715223 | 0.175059 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885116 | ACTCTGTTTCAAAAA[A/T]AAAAAATAAAAATAA | 7468 |
rs149232578 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979430 | TGCTCTTTGGAAATG[A/G]CTGTATCATTTTTTT | 7468 |
rs149237398 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895708 | GCTCTCCCGGGGAGA[C/G]GGGGGCTCCCCATGA | 7468 |
rs149281064 | snp | A/G | 3.29815e-05 | 0.00406075 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916974 | TTTTGAAGGAGAAGG[A/G]CAGTTTGAAAAATTA | 7468 |
rs149284685 | snp | A/G | 0.00136647 | 0.026103 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975361 | GGTCTGCCGGTGTGG[A/G]GCCTCCAATTGCAGT | 7468 |
rs149307984 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926608 | TCCTAGTAGCTGGGA[C/G]TACTGGTGCACGCCA | 7468 |
rs149309954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962222 | GTGTCAATCACAGGT[C/T]GTGGGGCTTACACCT | 7468 |
rs149319191 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909722 | CTCGGCTCACTGCAA[C/T]CTCCATTTCCCAGGT | 7468 |
rs149373250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950751 | TTCCAAAAAGCCTGT[C/G]TTAGTTCACCTACTA | 7468 |
rs149396950 | snp | A/G | 0.0103539 | 0.0712022 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901035 | AGAAATTAAGCTGAA[A/G]ATCACCAAAACATAC | 7468 |
rs149502776 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932780 | AAATCCATACAGATG[A/C]CCCTGTTGCTTGTTT | 7468 |
rs149583056 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905289 | AGTTTGAGCAAGTTG[C/T]GATGTGGCGAGTGCG | 7468 |
rs149588380 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878163 | CTTCCTGGGTTCAAG[C/T]GGTTCTCCTGCCTCA | 7468 |
rs149622038 | in-del | -/CT | 0.067446 | 0.170804 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892658 | CATTGTAACCTCCGC[-/CT]CTCGGGTTTGAGCGA | 7468 |
rs149647598 | snp | C/T | 6.5987e-05 | 0.00574362 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955204 | CGTTGCCTATCACAG[C/T]GGGGATGCTTGTCTG | 7468 |
rs149676700 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884132 | ATGGGGTCTTGCTCT[A/G]TCACCCAGGCTGGAG | 7468 |
rs149679248 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968107 | GACCTTGCATTCTAG[C/T]GCTCTGCTTATCTGT | 7468 |
rs149708402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903448 | GGAGCCGAGACTTGC[C/T]CCTAGTCCTCCTGGT | 7468 |
rs149758603 | snp | C/T | 1.74595e-05 | 0.00295456 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955736 | CCCAGCGGCCTTCCA[C/T]CCTGACTGCCTGAAC | 7468 |
rs149810908 | snp | A/C | 0.000561038 | 0.0167393 | missense | WHSC1 | GRCh38.p7 | 4:1935172 | GAAAAAAAGAAACCA[A/C]ACAAAGAGGATACAG | 7468 |
rs149836225 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888631 | GATTGCAGTGGCAAT[C/G]TCGGCTTACTGCGGC | 7468 |
rs149890243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923446 | AGAGCCAGTAAGTGC[A/G]TGAAGAGATGCTGCT | 7468 |
rs149921616 | in-del | -/A | 0.0770498 | 0.180522 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897493 | ACCCTGTCTCAAGGG[-/A]AAAAAAAAAATTGTT | 7468 |
rs149925711 | snp | A/C/T | 0.024414 | 0.107756 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978834 | CAAGACTGAGAAGCC[A/C/T]CCCCCAGAGCCAGGG | 7468 |
rs149952548 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875366 | GGCTCATTGCAGCCT[A/T]GATCACCTGGGCTCA | 7468 |
rs149971919 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897558 | GCACTTTGGGAAGGA[C/T]TCCTTGAAGCCAGGA | 7468 |
rs149980218 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981720 | TTGACATCTAAACCC[C/T]GGCGTGTGCAGTGCC | 7468 |
rs150048231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928791 | GGAATGTGCTGTGTT[G/T]GAGGAGGTGAGAGGC | 7468 |
rs150085904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943913 | CAGCTAGCCCATAAC[G/T]GATAGATGCATTAGA | 7468 |
rs150095706 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895319 | TTTGTTCAATGTTAT[A/T]ATCCCAACACCTAAA | 7468 |
rs150146753 | snp | A/G | 0.000131796 | 0.00811668 | missense | WHSC1 | GRCh38.p7 | 4:1904282 | CTGTTGAAATACAAC[A/G]TTGGTGATTTGGTGT | 7468 |
rs150147348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891268 | TGAAATATATTTCAG[G/T]CAGACTAGTGTGATA | 7468 |
rs150150439 | snp | C/T | 0.0178831 | 0.0928534 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974803 | ATGATGGTGAAAATT[C/T]CCTTTAAAAATAACA | 7468 |
rs150277175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959220 | TTGTTCATCAGCGAT[A/G]TGCACAGACACTAAG | 7468 |
rs150284974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873668 | CTAAAAGTAATCAAA[C/T]CTTACAAAGTTTACT | 7468 |
rs150294632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900275 | TCTTTTAAGTATATG[C/T]TGGTGGACAGGTGGA | 7468 |
rs150312094 | snp | C/G | 3.2962e-05 | 0.00405954 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951097 | GCCCGGGAGACGAGC[C/G]CTCGGAGTCCCCATA | 7468 |
rs150348745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978339 | CACAGCAGCCCCTGC[C/T]TGTCCACGCCGCGCT | 7468 |
rs150358384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932120 | CACATCATTGTCACG[C/T]GCCCATGACCTCAGT | 7468 |
rs150430277 | snp | A/G | 0.000499276 | 0.015792 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956100 | AGATTATTACTGGAC[A/G]CATCAGGCGCGAGTG | 7468 |
rs150487434 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914061 | GGAGTCTTGCTTTGT[C/T]GCCCAGGCTAGAGTT | 7468 |
rs150536286 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883403 | TTGGGAGGCTGAGGC[A/G]AGCAGATCACTTGAG | 7468 |
rs150590734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961738 | TGCCCAATCCTGACA[A/G]GTGTTGCCGGGCCCT | 7468 |
rs150594890 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879532 | CCTACACACATTTTT[A/T]AAAAAATGTGTATTT | 7468 |
rs150613164 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874672 | TGAAACATTGCAAGT[A/G]TATAAGTCCAACAAG | 7468 |
rs150665818 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950579 | GAAAGGACGCATGGT[C/G]TCCACCCCGGCGGCA | 7468 |
rs150684717 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935509 | TCTGCAAGAAAACAG[A/G]CATCCAAATGCTTTG | 7468 |
rs150746461 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923367 | AGGACACCATCGACA[A/C]AGTGAAAGGACAAAT | 7468 |
rs150797634 | in-del | -/A | 0.0399052 | 0.1355 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975517 | GTTGCCGGGACAGGT[-/A]GGGAGCAAGTTCCCT | 7468 |
rs150819100 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946599 | TAAAAGAAATATTCT[A/G]ATTCATATTTTAGGA | 7468 |
rs150876271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905002 | GGACGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 7468 |
rs150897030 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976989 | CTGTGGGGGCGGGGC[A/G]GCCAGGAAGGAGGCG | 7468 |
rs150925238 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877335 | AAATACAGATGTCCT[A/T]TGTGTCCCCAGTCTT | 7468 |
rs150979205 | snp | A/G | 0.00110777 | 0.0235087 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952089 | GGGCGCTGCTTACCC[A/G]CCTGCTCTGCCCCCG | 7468 |
rs150997550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937616 | ACACCCAATGTGCAC[C/T]GAGCACTTCTGACAT | 7468 |
rs151050778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973853 | GATTTCTCCCCACGC[A/G]GTTGTGCGGTGGATC | 7468 |
rs151054978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940737 | GCTGAGTCAGAAGGC[A/G]GCACTTCTGGCCAGG | 7468 |
rs151074276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925323 | TAGGGTCCCTAGATG[G/T]AAGGCTGACTTCAGG | 7468 |
rs151126791 | snp | C/T | 0.0012459 | 0.0249278 | WHSC1 | 4 | allele_origin=T(somatic)/C(germline) | 4:1918461 | CCTGGAGAGTCACCC[C/T]GACATAGGGAAGAGT | 7468 |
rs151137416 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913490 | CCACTTTCATGTTCC[G/T]CCCTGTACATCTGGC | 7468 |
rs151189148 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906723 | TAGAGTGCACTGGCG[C/T]GATCTCAGCTCACTG | 7468 |
rs151210647 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978019 | GTAATCCTGGCTACT[C/T]GGAAGGGTGAGGCAG | 7468 |
rs151213547 | snp | C/T | 4.95872e-05 | 0.00497907 | missense | WHSC1 | GRCh38.p7 | 4:1978769 | TGCACCCCGGACGGG[C/T]GGTCCTACTGCTGTG | 7468 |
rs151265726 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897349 | AGTTAGCTGAGCATG[A/G]TGGGGTGCACCTATA | 7468 |
rs151276826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885446 | GCGAGAGGGGGCCCT[G/T]GTCATTCTTGTAAGT | 7468 |
rs151286307 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970138 | GCAGGCCAGAGGATG[A/G]TTCAGCGGGGCTGAG | 7468 |
rs151337221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964046 | CTTAAACGTTTACAA[A/C]GCGCAATAGAAGGTG | 7468 |
rs180696589 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981430 | TGAACATCAGCTTCA[A/G]TCCTCCATCATTAAT | 7468 |
rs180723416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941138 | AAATTATTTTTCCTT[C/T]TTCCTTTCTTTCTTG | 7468 |
rs180725047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972019 | GTACCCCCAAGGCTG[C/T]GGGTGCTGGGTGATG | 7468 |
rs180730979 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925791 | TTTTTTGTTTGTTTG[A/T]TTGTTTGTTTGTTTT | 7468 |
rs180748518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960907 | GGAGACTTTGTACAC[A/G]CCCTCCACGGAGGTA | 7468 |
rs180754158 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894412 | CACCTCTTTGAAATT[C/T]GTTGGCTGGCTGAGG | 7468 |
rs180756901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932789 | CAGATGCCCCTGTTG[A/C]TTGTTTCTGTAAGAA | 7468 |
rs180757123 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918996 | CTACAAAAATTAGCC[A/G]GGTGTGGTGGCACAT | 7468 |
rs180761566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878045 | AGAAAAATAAAATTT[A/T]AAAAAAGTATTATAT | 7468 |
rs180769981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910170 | GTAATTTACAGCAGC[A/G]GAACCTGTGTTAGCT | 7468 |
rs180772163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949847 | TAATTTGTTTTTCTT[C/T]CACCGCTCCCTGCAA | 7468 |
rs180776397 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884220 | CCCACCTCAGCCTCC[C/T]AAGTAGCTGGGACTA | 7468 |
rs180779244 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921473 | AAATTAAAAAAAAAA[A/G]GCATTCTCTTTAAAA | 7468 |
rs180812884 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902041 | GGCTTTGGCAGAAGG[A/G]AGGAACTCTTGATGG | 7468 |
rs180859260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906224 | CTCCTTGTTCTTCCT[A/G]TTAGGGCTTATTACT | 7468 |
rs180891488 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930487 | TTCTTTGAAGCTTTT[A/G]TGGACATAGTTCCAC | 7468 |
rs180898393 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945567 | CTGAGAAGGCTCTTG[A/C]CAGAAGCCTGATGTG | 7468 |
rs180901430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966611 | GCAGTGAGCCAAGAT[C/T]GTGCCAGTGCACTCC | 7468 |
rs180904041 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897823 | GTAGAGTTGTGGTTT[C/T]ACCATGTTGGCCAGG | 7468 |
rs180908347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889930 | AGTTGCTACTACCTA[A/G]TTCCTAAACATTTCA | 7468 |
rs180908892 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880718 | GAGTTGCCATTGGCA[A/G]CACTGAGAAATGTGG | 7468 |
rs180917404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922764 | AACCTTATCTCTACT[A/G]AAAATATAGAAATTA | 7468 |
rs181264681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936384 | TTTTATTCGATAATA[G/T]TTCTGGCCGGGTGTG | 7468 |
rs181275065 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951657 | AGGACCCCAGCCAGG[C/G]CACCTACACTCTGTG | 7468 |
rs181277570 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977853 | AATCCAGGCCAGGCA[C/T]GGTGGCTCATGCCTC | 7468 |
rs181293007 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973384 | ATGTCCCATGTGCAT[A/G]CCCCGTGCTGTCCTC | 7468 |
rs181310238 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933415 | TCTTTGAGTTGGAGT[C/G]TTGCTCTGTCGCCCA | 7468 |
rs181333290 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957294 | TTTGTTTTTGTTTTT[G/T]TTTTTTTGAGACTGA | 7468 |
rs181418225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955457 | GACAGTGTTCTGTGC[A/G]TCTTCACGTTAATAG | 7468 |
rs181418723 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960641 | GCACCCTTGTTCCTC[A/G]CCTGCCTGACTGCTG | 7468 |
rs181419871 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977573 | CTGAGGTCAGGAGTT[C/T]GAGACCAGTCTGACC | 7468 |
rs181430285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877181 | AGAGGATCTGTGCAT[A/G]TTAGCAATGTTCTTA | 7468 |
rs181436965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925691 | GGCCTGAGCCACTGC[A/G]CCCAGCCTAGAGGTC | 7468 |
rs181445554 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935715 | AAATACAAAAAATTA[G/T]CTGGGCATGGTGGCG | 7468 |
rs181445755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922333 | AAAAGATACCATTGA[C/T]AATAGAAACCAAAAT | 7468 |
rs181533808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940318 | GTTACTTGAGTGTTG[A/C]GGTGAGTCAGAACTA | 7468 |
rs181544331 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980255 | TCTGAGTACTACATA[C/T]GTTTTAAGACTTGGT | 7468 |
rs181548499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880314 | TGAAGTTAGAACTCC[C/T]GCAGGGCCTGACCTC | 7468 |
rs181555761 | snp | A/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919433 | TTCTTAATTGTTTGC[A/T]TAAAATGCACAGTCT | 7468 |
rs181559116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939548 | AGGACAAAGGAATTC[A/G]GAAGATTCATCTTTA | 7468 |
rs181568032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933066 | CCCCAGACTGCCTTT[A/G]CACCAGCCTGCAGTG | 7468 |
rs181577342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902214 | TAATGGCAGTGGTGA[A/T]GTTTTTAAATTTTAT | 7468 |
rs181580861 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884349 | GATCTGGCCCACCTT[C/T]GCCTCCCAAAGCACT | 7468 |
rs181581818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909613 | AAGCCAGTACTTTTA[C/T]ATTTTTCTATCCTCT | 7468 |
rs181648487 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889026 | CCTCAGCCTCCCGAA[A/T]AGCTGGGATTACAGG | 7468 |
rs181695047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905459 | GTGGTCCTTGCGTAC[A/G]TGTCCCCTTCTGGTC | 7468 |
rs181708497 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872833 | AAAATAACTTAGGAG[A/C]CATCCCATTTATGAA | 7468 |
rs181747125 | snp | A/C/G/T | 0.00279258 | 0.0372817 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909265 | GTTTTTCCCACCACC[A/C/G/T]CCCCCAACCCTAGCA | 7468 |
rs181794645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876060 | CTCTACTAAAAATAT[A/G]AAAAATAAGCTGGGC | 7468 |
rs181938529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950889 | ACATAGCCTAATTGA[C/T]GGGTTATATTATCAC | 7468 |
rs182003566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922021 | GGCGTGGTGATGCGC[A/G]CTTGTAATCCCAGCT | 7468 |
rs182008601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905104 | CATTGCACTCTAGTC[C/T]GGGCAACAACAGCGA | 7468 |
rs182019510 | snp | C/T | 0.0025966 | 0.0359383 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935289 | CCAGGTTTGCTTGAC[C/T]TGTCAGAGTGTATGC | 7468 |
rs182025289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924735 | GGGCAACACAGTGAG[A/T]CTCTCATCTCTACAA | 7468 |
rs182035777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888767 | GATGGGGTTTCACCA[C/T]GTTGGCAAGGCTGGT | 7468 |
rs182037284 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872456 | TGTATAGGACCCATT[A/G]CAGCACGAATCTTTC | 7468 |
rs182042544 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892810 | CTGACCTTGTGATCC[A/G]CTCGCCTCAGCCTCC | 7468 |
rs182047460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943346 | ATTAAGTAATGTAAC[A/G]CATGTAAGATGCTTA | 7468 |
rs182052530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963627 | TTGGTTCCTGACATG[A/G]TAATCCACCTGAGGT | 7468 |
rs182080307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927883 | TTCCATGTTTTTTTG[A/G]TATGTTTTAAATTTT | 7468 |
rs182090559 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972792 | GGCAGCTTTGTGAGA[A/G]AAGACATTGTGCACG | 7468 |
rs182244177 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930524 | GGAATAAAAATGCGA[A/C]ACACTAAGTTCTAAA | 7468 |
rs182245560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955099 | AGTAATTATTAGTTG[C/T]TCTTTTCACTATGAC | 7468 |
rs182308802 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898285 | TGAGATGGGCTCTCA[C/G]TGTCTTGCCCAAGCT | 7468 |
rs182328348 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873647 | TATTCAGATTATCTT[A/C/T]TCCTTCTAAAAGTAA | 7468 |
rs182383701 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952832 | TCCTGCCTACTCACC[A/G]GGCCCAAGGAGTCTC | 7468 |
rs182445092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920579 | CCTGTATTTATGGGG[C/T]ATATGTGATATTTGG | 7468 |
rs182458353 | snp | A/G/T | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885662 | GCCTAGCTGCTCTTC[A/G/T]TGGCTGTGCCTTCTT | 7468 |
rs182487265 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948198 | CTCGGAGCTCAGTGC[C/T]GCAGCATGGCTGTGG | 7468 |
rs182489476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970164 | CTGAGTCACATTGGG[C/T]GACGTCGTAAGTAGG | 7468 |
rs182510732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916328 | AGCTAGCTAGCTTTT[G/T]TCTTTTTCTTTTTTT | 7468 |
rs182514418 | snp | A/G | 0.0655868 | 0.168795 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898655 | ACAGAGCGAGACTCC[A/G]TCTAAAAAAAAAAAA | 7468 |
rs182523477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976241 | TGAGATGCGTCATTG[C/T]AGGCTTCCGACAAAG | 7468 |
rs182523593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915708 | TCCTTTGCATTAGAG[G/T]GTCTGATTGGCCATT | 7468 |
rs182524384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931484 | AAAACTGAGATTTGA[A/G]TGTAAAAATAACTGA | 7468 |
rs182547619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946111 | AATTGCTGAGGTGTG[C/T]GGTTTATCTTTGAGA | 7468 |
rs182554255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881283 | TCTGTTTTTTTGAGA[C/T]GGAGTCTTGCTTTCC | 7468 |
rs182594531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881744 | TGTTTAGAATTCCTC[A/G]TCACACAAAGCAAGT | 7468 |
rs182632081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911951 | GTTTAATTTTATATT[A/G]TGTGTGCTGTTACAG | 7468 |
rs182641017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933995 | AACATGTTTAAGGAA[A/G]TGTTTAAAAAGTAGC | 7468 |
rs182644456 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920079 | GACTGTGAGTATTCT[A/T]ATAAATCTACTGGAC | 7468 |
rs182647449 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973702 | TGGGTGCGTGGGCAG[G/T]TGTGTCAGAGGCCGC | 7468 |
rs182656865 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895608 | TCTCCTGTAGAAGAC[C/G]TTCCATACTGTCCCA | 7468 |
rs182762854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915943 | CTTACCTGTATTCAC[C/T]TTCTCATTTGACTTC | 7468 |
rs182787950 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898584 | CAGGAGAATTGAACC[C/T]GGGAGGTGGAGGTTG | 7468 |
rs182796906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881376 | TACGCCATTCTCCTG[C/T]CTCAGCCTCCCCAGC | 7468 |
rs182854230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978464 | GAGTCAACAGGCCCT[G/T]CCAGGGAGCCCGCCC | 7468 |
rs182891732 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937824 | CAGTTTTCAGCCACA[C/G]CTTTCAGAATCTCAG | 7468 |
rs182916097 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979144 | CTGGACAAACAGCCT[C/G]ACTCCTCAGCGTTAC | 7468 |
rs183083577 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962167 | CAGTAGTGGGGCAGC[A/G]GTGGCCAGTGGAGCC | 7468 |
rs183110331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927440 | ATGTTGGGGGGAGCA[C/T]AGTGCAGTGCCTCAT | 7468 |
rs183134365 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902981 | GGAGTTCAAGACTAG[C/T]CTGGGCAACATAGCG | 7468 |
rs183257236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923636 | ACATCATTTATTACA[A/C]CTGTTTTGAGAGAAA | 7468 |
rs183290751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890851 | GATCACCTGCCTCAG[C/T]CTCCCAAAGTGCTGG | 7468 |
rs183301652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946843 | TCCAACAGCCCGACA[A/G]GCCTCATCTTTTTGG | 7468 |
rs183336519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934315 | GTCTCAAACTCCCGA[C/T]CTCAGGTGATCCGCC | 7468 |
rs183336655 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982366 | GCCACCTTGGGAAGT[A/G]TAACAACAAATACTG | 7468 |
rs183341632 | snp | A/G | 8.56054e-05 | 0.00654182 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953186 | TTGGACTAGTGAGCA[A/G]GGTTGGAAACAGGGC | 7468 |
rs183355952 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886088 | TTTCCTTTACGAAAC[G/T]AAAGCGCGTCCATTG | 7468 |
rs183362848 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920996 | TGAACCATGATCATG[C/T]CATTGCACTCTAGTC | 7468 |
rs183364620 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961425 | CCTTAGTACAGGGCA[A/C/G]GGAAGTAGAGAGGAC | 7468 |
rs183366871 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904109 | CACACTCCATTTTTG[G/T]GGGTCTGTGTGTATT | 7468 |
rs183382156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942549 | GAAGAAAACAGATAA[A/C]AAATTTTAAGACCAA | 7468 |
rs183433399 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885193 | CTGCTTGTTTGTCCA[C/T]TATCTACCTTTTTAG | 7468 |
rs183435989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878409 | CACCATGCCTGGCCA[A/G]AAAAACTTTTTTTAA | 7468 |
rs183441170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911655 | GAAGGGAGGATTACT[A/G]ATAACATAGTACTGG | 7468 |
rs183460701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978058 | CTTGAACCCAAGAGA[C/T]GGAGGCTGCAGTGAG | 7468 |
rs183489860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937598 | TGAGCCAAACCACAT[A/G]TGACACCCAATGTGC | 7468 |
rs183490871 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870295 | CTTGACCAAACTCTC[A/G]CCAGGCTCCCCTGGG | 7468 |
rs183494089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888483 | TATCCTCAGCTGATA[A/G]CTTGGTTGGGTATAT | 7468 |
rs183495103 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969488 | GAGAACCGCTTGAGC[C/G/T]CAGCCTGGAGTTTGA | 7468 |
rs183504706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957502 | CATGTTGGCCAGGCT[G/T]GTCTTGAACTCCTGA | 7468 |
rs183510296 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896132 | GATTCTAGTCCAGAC[A/G]GCAGCTCCACACTTG | 7468 |
rs183515765 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890569 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 7468 |
rs183526318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907167 | TGAAAATGAGGAAGA[C/T]GATACCATCACCTTC | 7468 |
rs183539071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874661 | TAAGGTCACTCTGAA[A/G]CATTGCAAGTATATA | 7468 |
rs183540251 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875184 | CTGGTCTCTGTAACT[C/T]CTGGCCTCAAGTGAT | 7468 |
rs183541691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907859 | CTTGTGATCCACCCA[C/T]CTTGGCCTCCCAATG | 7468 |
rs183542587 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930877 | GTCCACTCTCCCTGT[G/T]TCTGACCCGTGGGGT | 7468 |
rs183702648 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895059 | TTTGTGTCTGCCTTA[C/T]TTCACTTAGCATAGT | 7468 |
rs183834501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973891 | TCCTCAGGTGGAGGC[C/T]GGGGCCGTCCATTCC | 7468 |
rs183835773 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955028 | TCTGAAAGCTTTTTT[C/T]AAATCAAATACCTCC | 7468 |
rs183874071 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941913 | CAAAGTGTAGTGTTA[C/T]AAAAAACAGCCTGTT | 7468 |
rs183970043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970677 | TTCAGGAGCAAAGGA[A/G]AGCATGAAGATAATG | 7468 |
rs183983458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875236 | AGTACTGGGATTACA[A/G]GTGTGAACCACTGTG | 7468 |
rs183983648 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891389 | GGTTGGAGCTTGGTC[C/T]GTCTCACGGCCTGGC | 7468 |
rs184002347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899410 | GGTCAGGGTCCGCCC[C/T]CTAGTGGTGGTAATA | 7468 |
rs184012968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932172 | CTGGGCACGGTGGCT[C/T]ACACCTGTAATCCCA | 7468 |
rs184027526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927159 | GGCCCTCTCCACAGG[A/G]CTGCTGGTGTGTCCT | 7468 |
rs184075552 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971899 | AAACCAGGACTACAA[C/G]TATGCTTAGCTTGCT | 7468 |
rs184095879 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932736 | ATGGAATGGCCAACA[A/G]GAGCGAAACTCCATC | 7468 |
rs184100109 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921767 | AGCCTGGGCAACACA[A/G]CAAGACTCTGTCTCA | 7468 |
rs184107326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949556 | TCACGAGGTCAGGAG[C/T]TCAAGACCAGCCTGG | 7468 |
rs184127476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1954783 | TTCTTGACACCAGTG[A/G]TTCTTTATCGGGCAA | 7468 |
rs184129247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948292 | TCCTTTCCAAATGCA[C/T]CTCGTTGGATATGGA | 7468 |
rs184141980 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918007 | GCTGGTCTTAAACTC[C/G]TGGCCTCAAGTGATC | 7468 |
rs184169167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916741 | GGAAGGGATAAGAAG[C/T]ATAGAATTTGTTTTG | 7468 |
rs184188004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882557 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7468 |
rs184226810 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974502 | TACAGGCGTGAGCCA[C/T]TGCGCCCAGCCAGGG | 7468 |
rs184231292 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930356 | TGGAAAAGTATATAT[A/G/T]TATTTTTATCATTTA | 7468 |
rs184249976 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934632 | AGGCAGGCGGATCAC[A/G]AGGACAGGAGTTCGA | 7468 |
rs184252047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897383 | CCAGCTACTCGGGAG[A/G]CTGAGATGGGAGGAT | 7468 |
rs184266571 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914673 | ATTGATGGTTTGACT[A/G/T]GGTGTAGAATTTTAT | 7468 |
rs184266972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954144 | CACGTGCCACCATAC[C/T]TACCTAATTTTTGTA | 7468 |
rs184269531 | snp | C/G | 3.32358e-05 | 0.00407637 | missense | WHSC1 | GRCh38.p7 | 4:1935149 | CCATTCCAAGGTAAT[C/G]TAAATGGGAAAAAAA | 7468 |
rs184277377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880332 | AGGGCCTGACCTCTG[A/G]TTCTGTACCCTGGGA | 7468 |
rs184284304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904853 | TAAGAATGTACGGCC[A/G]GGCACGGTGGCTCAC | 7468 |
rs184323339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879684 | GCCCTGTCCCATGGA[C/T]CTTTGCATGTGCTGT | 7468 |
rs184352566 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949060 | CCAGACAGTGTGGCC[A/G]CTGCTTCCCCATGCC | 7468 |
rs184368968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900200 | TTTTGCTTTTATGCT[A/G]TTCCCTGTTGTCCTT | 7468 |
rs184377066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883374 | CAGTGGCTCAGGCCT[A/G]TAATCCCAGCACTTT | 7468 |
rs184381018 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917265 | TCTCAGAGATAACTT[C/G]TTTTAGAATTTATAT | 7468 |
rs184511643 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980206 | TTCACTTTAGTTTTT[A/G]AAAGGTCCAGTTCTA | 7468 |
rs184625941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977179 | TGCACCAGGAGGCTC[C/T]GCCGGTTGACGAAGG | 7468 |
rs184638606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922209 | TGTTTGCAGAAGTCT[A/G]TGTAGAAAACTCAAG | 7468 |
rs184646767 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905267 | TTCTAGAGTGAAGTT[A/G]GAATTTAGTTTGAGC | 7468 |
rs184647094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935582 | ATAACCTCTTTGGCC[A/G]GGTGTGGTGGCTTAC | 7468 |
rs184669783 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975849 | CTTAGCGCCTGCCCT[G/T]CTACCGTGTGACCCC | 7468 |
rs184676394 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888845 | TACTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 7468 |
rs184702774 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883826 | GAGCTGCCTAGATGG[C/T]GATAAGAAGCGAGTG | 7468 |
rs184707143 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908449 | ATAATATACTTTTTT[G/T]TGTGTGTGAAGGCAT | 7468 |
rs184728514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938769 | AAATTTTATTGAAGT[C/T]ACTTTTTACTTGGCT | 7468 |
rs184761337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958881 | CTTTCGCCACCTCTT[C/T]CCTAAGATTATGCAT | 7468 |
rs184764300 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979691 | CTCGCTAGGTTCTTA[C/T]CAACATTTGGGGGAT | 7468 |
rs184773372 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909084 | AAAAAAAAAAGAGTT[A/G]TATATTTTAGTTCTT | 7468 |
rs184780840 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939297 | AGTAGCATTGTGGTT[A/G]TATGTAAGACTTTAT | 7468 |
rs184786781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924215 | AAGTAATCAGCAATG[C/T]GTGTACAGCCACCGT | 7468 |
rs184805121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892449 | CAGGTAATACTGTAT[A/G]TATTCCATGAAATGT | 7468 |
rs184811230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875822 | GCTGAGGCAGGAGAA[C/T]GGCGTTAACCCAGGA | 7468 |
rs184818023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958646 | GTGTGCCGGAGGTCA[C/G]GTGCTCTGCCTTTGC | 7468 |
rs184837752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965224 | AAACTAAAGGAAAAC[A/C]TGCAGAAAGTCAAGA | 7468 |
rs184840987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923836 | CATCAATTAAAGTGA[A/G]CTCATTGGATGTCAA | 7468 |
rs184889124 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869571 | TAGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7468 |
rs184937337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945474 | AAAGAAAACTAAGAT[C/T]ATAAATTAGCATCTA | 7468 |
rs184965980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921519 | AGGCACAATGGCTCA[C/T]ATCTGTAATCCTAGC | 7468 |
rs184985997 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892818 | GTGATCCGCTCGCCT[C/T]AGCCTCCCAAAGTGC | 7468 |
rs184988724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887010 | TTGTGGTGGTTTGAT[G/T]ATCTATTCCAGAACT | 7468 |
rs184995385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924741 | CACAGTGAGACTCTC[A/G]TCTCTACAAAAAAAA | 7468 |
rs185083960 | snp | A/C/G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909269 | TTCCCACCACCCCCC[A/C/G/T]CAACCCTAGCATCAG | 7468 |
rs185105154 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971230 | AAGGTATGCCAAGGT[G/T]AAGTCGAAGAAAGGA | 7468 |
rs185122539 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873990 | CGCCTCAGCCTCCTG[A/T]GTAGTGGTTACTACA | 7468 |
rs185127639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876106 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 7468 |
rs185133256 | snp | A/G/T | 0.0142791 | 0.083329 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915379 | TCGGCCTCCCAAAGT[A/G/T]CTGGGATTACAGGCT | 7468 |
rs185348604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960220 | TGTTACATGAAAGGT[A/G]TCTGCTATAACTCAC | 7468 |
rs185354317 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951690 | TCAGTCCCGCCCCAT[C/G]TGTCAGCTGGAGATG | 7468 |
rs185360294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973399 | GCCCCGTGCTGTCCT[C/T]GTCCCCAGGGCCCTG | 7468 |
rs185470393 | snp | C/T | 1.69714e-05 | 0.00291298 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939621 | ATCAAGGGTTTATGA[C/T]TTGAAACTTTACAAA | 7468 |
rs185488808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906299 | ACTGGAGTGCAGTGG[C/T]GCAGTCTTAGCTCAC | 7468 |
rs185494490 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944565 | GTGTAAAACTTGAGG[C/T]ATTCACTAGAGGTGA | 7468 |
rs185495768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915996 | CTTTTATTTTGGGCC[C/T]GTCTCTTTCTTTCCT | 7468 |
rs185496043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930511 | GTTCCACGATGTGGG[A/G]ATAAAAATGCGACAC | 7468 |
rs185503523 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945694 | AAAAGTCCTTGGCTC[G/T]TTTGATCCAGTTGAG | 7468 |
rs185505217 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966777 | TTAAGCTACTCATGT[A/T]TTACTAGTTTTACTC | 7468 |
rs185507250 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956614 | CTTGGCCTCTGATTC[C/G]CCAGCTGGGGTGGGA | 7468 |
rs185509425 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913411 | TCAGTCAAGCCCACC[C/T]GCAGCCATCCAGAGG | 7468 |
rs185512629 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977785 | CGACAGAGCAAGACT[C/G]CACTCAAAAAAAAAA | 7468 |
rs185513809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947038 | TGGGGGTCCTGGTCC[A/G]GCTGATGGGGGTTTG | 7468 |
rs185516993 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930938 | CAGTAAAAACAGCTT[C/T]TGCCATCTGCGTTTA | 7468 |
rs185533999 | snp | C/T | 0.0659589 | 0.169201 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898646 | ACCTGGGTGACAGAG[C/T]GAGACTCCGTCTAAA | 7468 |
rs185544758 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881453 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 7468 |
rs185548332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880182 | GTAATCTTTGTAGAG[C/T]CTTGCTACACAAATC | 7468 |
rs185582919 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972488 | GTGGGAAGGGTGGGC[A/G]TGTCCTGGGGGTGAC | 7468 |
rs185630679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964508 | TTCTTGGAGCACCTC[A/G]CACACAGCTTGAGGG | 7468 |
rs185638330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894015 | AGGTTGCTGTAGCCT[C/T]GAATTCTTAGGCTTA | 7468 |
rs185644805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896763 | TTCTTTCTTTCCTTC[C/T]TTCTTCTCTTTTTTT | 7468 |
rs185646567 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925762 | CTTCTTTTTATATAT[A/C]TATATATATATTTTT | 7468 |
rs185650940 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929405 | AGTGTTACTGCCCCC[A/G]TTTCACAGAGTGGAG | 7468 |
rs185654145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910084 | ATAAGCTACAGCTCA[A/G]TCTAGATTCTTTTGG | 7468 |
rs185670401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877265 | CAGAAAGCATTTTTC[C/T]GACTCCGGTTTTACT | 7468 |
rs185690509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884644 | CGATCTGCCTGCCTT[A/G]GCCTCCCAAAGTGCT | 7468 |
rs185758530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1950243 | GGGTGAGGCTGAGGC[C/T]GTATTCAGCCTGGTC | 7468 |
rs185777225 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897853 | GCTGGCCTCGAACTC[C/T]AGACCACAAGTGATC | 7468 |
rs185893904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880734 | CACTGAGAAATGTGG[A/G]AAACTATAAGACCAG | 7468 |
rs186016067 | snp | A/G/T | 0.00186201 | 0.0304566 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951233 | GCATCCGCTATGTCC[A/G/T]TGCTGGTGTCTGACT | 7468 |
rs186019761 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973233 | ACAGGGTCAAGACAT[G/T]GCGGGCAACCCACAG | 7468 |
rs186038165 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919494 | GAAGGAGTTGGGTTC[C/T]CCACTTCCCACTTTT | 7468 |
rs186046703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902516 | GGTATGAGCTACCAT[G/T]CCCAGCCTACAAAGA | 7468 |
rs186060965 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933328 | GCTGGTGTCTCCTGT[C/G]CCAACAGTAGTGAGG | 7468 |
rs186120998 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957398 | AAGCAATTCTCCTGC[C/T]TCAGTCTCCCAAGTA | 7468 |
rs186142087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923159 | ATAAGCCAAACTAAT[A/G]ACAGGCTATAAAGGC | 7468 |
rs186230438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872533 | AACTGATGTGGTGAC[A/G]TTAATCGTTTTTAGG | 7468 |
rs186246192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937211 | TGCGTGCCACCATGT[C/T]CAGCTAATTTTTTTG | 7468 |
rs186253588 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940774 | CCATGGTCCCCAGGA[A/G]GGATGGGGTGTGCCT | 7468 |
rs186255003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977961 | GTGAAACCTCATCTC[C/T]ACTGAACATAGAAAA | 7468 |
rs186273867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920374 | AGAATCACTTGAACC[A/G]GGAGGCCACAGTGAG | 7468 |
rs186273932 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980959 | ACACACCTTAGAGTC[A/G]AAGGCCCCAGGGCCC | 7468 |
rs186299367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885445 | TGCGAGAGGGGGCCC[C/T]GGTCATTCTTGTAAG | 7468 |
rs186319286 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978063 | ACCCAAGAGACGGAG[A/G]CTGCAGTGAGCCAAG | 7468 |
rs186356919 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969982 | GAACCACAAGAACGG[C/T]ACGAAGGTGGATGTG | 7468 |
rs186377303 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935729 | AGCTGGGCATGGTGG[C/T]GTGCACCTGTAATCC | 7468 |
rs186398045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905971 | CAAGCCTCTGCAGCC[C/T]GGGTGCAGGCACACA | 7468 |
rs186422598 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902989 | AGACTAGCCTGGGCA[A/G]CATAGCGAGACCCGG | 7468 |
rs186425934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960800 | TGTAGGAAGCAAGGG[C/T]TGGCATATTGCCACT | 7468 |
rs186440343 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981502 | CTTGGCATCCGAAAC[C/T]AGCATCTGCACCTAA | 7468 |
rs186447262 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872919 | ATTTAAATGTGATGA[C/G]AACAACAATATTTTA | 7468 |
rs186460435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941195 | AATTAAATGAAAGGT[C/T]ATTTACAGTTCCAAA | 7468 |
rs186465432 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926503 | TGAGACAGGGTCTCA[C/T]TCTGTTGCCCAGGCT | 7468 |
rs186475473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894796 | TTTGGGGGTATACGT[A/G]ACATAAAATTTACCA | 7468 |
rs186489219 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910320 | AACCTCTGTCTCCCA[C/G]GTTCAAGTGATTCTC | 7468 |
rs186628136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922475 | CTTCTGAAGTTGTCA[A/G]TTCTCCCTTTAATAA | 7468 |
rs186638139 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943940 | TAGAAGTCAGCCAGC[A/G]CATAGGTGCTCCCTC | 7468 |
rs186638445 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963872 | AAAAAATTAGCCGTG[C/G]CTGTGATTCCAGCTA | 7468 |
rs186652720 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889131 | TGGAACTCCTGACCT[C/T]AGGTGATCCACCCGC | 7468 |
rs186766130 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948228 | GTGGACGCGGGAAAC[A/C]ACGGGAAAGTTCTTG | 7468 |
rs186769497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923910 | TGTAGTTTGAAAAGG[A/G]CCACATACCCACAAC | 7468 |
rs186772846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908580 | GAAAAGGGGTCAAAG[A/G]AAGTGAGCAGAACAA | 7468 |
rs186777528 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970328 | TGGGCTCCTCAGAAC[C/G]AGCCAGGGGTGTCTA | 7468 |
rs186798810 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931525 | TATCAATTTAAAATT[A/T]AAAAAAAAAGTACTG | 7468 |
rs186804708 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891443 | CACTGCTGTCCTAGG[A/G]TTGAGACCTCCTTCT | 7468 |
rs186806227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875439 | GGCATGTGCCACCAT[G/T]CCTGGCTAATTTTTG | 7468 |
rs186898260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912068 | AGAAGTCACAAATCC[C/T]TTGACATATCCTTGA | 7468 |
rs186903756 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943185 | TTTGCATGGTAAGGA[A/G]AAGGCTTACTTGCCC | 7468 |
rs186908483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961601 | AGCCCATATTTCTAA[C/T]CATTTTGGAACCTAG | 7468 |
rs186910220 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927658 | CAGGAGGCAGAGGTT[G/T]CAGTGAGCTGAGATC | 7468 |
rs186913920 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879477 | GCCCGCCTCGGCCTC[C/T]CAAAATGCTGGGATT | 7468 |
rs186929389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927311 | CGCCGTAAGCAGTAG[C/T]GGGGGCTTGAGCTCT | 7468 |
rs186931128 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895729 | CTCCCCATGAGCAGT[G/T]CTCAGGTTTCCCTGC | 7468 |
rs187002165 | snp | C/T | 0.000167628 | 0.00915346 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974792 | CAATGTGCTTTATGA[C/T]GGTGAAAATTCCCTT | 7468 |
rs187104128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915743 | ACTTAATTGGGGGAA[C/T]CTCCAGAAGACTCAC | 7468 |
rs187107158 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982450 | GAAATAATTTGCTTC[C/T]CAAATTCCCATTAAG | 7468 |
rs187109025 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946353 | GCTCACTGCAACCTC[C/T]GCCTCCTTGGTTCCA | 7468 |
rs187149066 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941951 | GGGCCCGATTCTGAT[A/G]TGAGTTAGGTGACCA | 7468 |
rs187251615 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878230 | CATGCCCGGCTGATA[G/T]ATATATATATATATA | 7468 |
rs187256536 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967832 | TCAACAGGCAGCAGG[A/T]GGTTGGATGAGGGGT | 7468 |
rs187274246 | snp | A/G | 3.65384e-05 | 0.00427409 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930579 | AAACAAAACCCAATG[A/G]GTTTTACGGATTTAA | 7468 |
rs187274900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932898 | CGCCTGTGGGAAAGC[A/G]AGGCGCGGGGCTGGC | 7468 |
rs187307808 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902113 | TTTTTAGTTGTAACT[A/C]CTTGAAATTGTTAAA | 7468 |
rs187334767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898338 | GTGATCCTCCTGCCT[C/T]GGCCTCCCAAAGCCT | 7468 |
rs187464971 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919320 | AGTGCAGGATATGCT[C/T]ATCTGTAAAGCTCAT | 7468 |
rs187501518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884268 | GCCTGGCTAATTTTT[A/G]TATTTCTTGTAGAGA | 7468 |
rs187504628 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979085 | ATCCTCAGCAGCGTC[C/T]GCTGCGTCTGCACTG | 7468 |
rs187513553 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971235 | ATGCCAAGGTGAAGT[C/T]GAAGAAAGGAGTTGT | 7468 |
rs187619937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934480 | CCTGAGCTACAAGAG[C/T]GAAACTCCATCTCAA | 7468 |
rs187630867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953201 | AGGTTGGAAACAGGG[C/T]CAGGTGCTTTAGCAG | 7468 |
rs187638757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974084 | CCTCATCTCAGCCAA[C/T]GCCACATCAGCGCCA | 7468 |
rs187652386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886598 | GCACTTTGGGAGGCC[G/T]AGGCGGGCAGATCAC | 7468 |
rs187659236 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921367 | GGGAGGCTGAGGCAG[A/G]AGAATTACTTGAACC | 7468 |
rs187681609 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958683 | AATGTGGGCTGCAGT[C/G]AATATCTTTGTATGT | 7468 |
rs187741323 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898785 | ATTTGGGCAGAGTTT[A/T]TAGGCAGAATTTGGG | 7468 |
rs187774719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937741 | GGCAGGTGGGTGAGA[C/T]GGAGTATGAGTGCAG | 7468 |
rs187777470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928547 | CTCTGTTAACCTCAG[A/G]TGATGATGACACTTT | 7468 |
rs187780780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923580 | CAGCCAGGGATTGAG[A/C]AGATGAGCAACAGTG | 7468 |
rs187784764 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957643 | CAGGCTTTGACCCTG[A/G]TGCTTTGTCCTTAGG | 7468 |
rs187799322 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890682 | TCTCGGCTCACTGCA[A/G]CCTCCGCCTCCTGGG | 7468 |
rs187809533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882619 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 7468 |
rs187815837 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907303 | CCCCTGGTTTCTTCT[A/G]TAGCTGCTTCCTGAA | 7468 |
rs187845238 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921651 | ACCAGCTGTGGTGGC[A/G]AGCGCCTGTAATCCC | 7468 |
rs187856179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954157 | ACCTACCTAATTTTT[A/G]TATTTTTAGTAGAGA | 7468 |
rs187920210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903995 | CACGTTGGCCTCCCA[A/G]AGTGCTGGGACTACA | 7468 |
rs187930311 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885911 | TTTCCAGAGATGTGC[A/G]ATTTGACACATCATT | 7468 |
rs187975852 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979158 | TCACTCCTCAGCGTT[A/G]CCGCCACACTTGAAT | 7468 |
rs188001915 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938311 | TGCCACGAAACTTTT[C/T]AGCAACCTGTGTTCA | 7468 |
rs188003692 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939036 | TTTTACCTTTTAGTT[A/G]TCTTTTTGAAATACC | 7468 |
rs188019389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908255 | CCAGGTTGGATCTCA[C/T]AGTTGGAACCTTGAA | 7468 |
rs188019971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916389 | CTAGCTCTGTCACCC[A/G]GGCTGGAGAGCAGTG | 7468 |
rs188023545 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875222 | CCTTGGCCTCCCAAA[C/G]TACTGGGATTACAAG | 7468 |
rs188058323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882066 | CTATTTGCTTTGGAA[A/G]GAAGATTCCTCAGAT | 7468 |
rs188115487 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963001 | TTCTCTAGGAGGTGG[G/T]CTCTGGCATACCCTA | 7468 |
rs188119588 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934728 | TGGCACGTGCCTGTA[A/G]TCCCAGCTACTCAGG | 7468 |
rs188130234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921913 | CAACACTTTGGAGGC[C/T]GAGGTGGGTGGATTA | 7468 |
rs188156836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904652 | TTATTATTTAGTTAC[A/G]ATGATTGCTTGTTTC | 7468 |
rs188256876 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967179 | TTGGATAACTGAGAT[A/G]AAATAGACAAATTCC | 7468 |
rs188260513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945813 | AAGCCACGGATTCCC[C/T]TCGCTGGAGAGGCTC | 7468 |
rs188274472 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923664 | AAATTTGGCAAGATC[A/T]AGTGAAATTGAAGAT | 7468 |
rs188284129 | snp | A/C/G | 0.00028152 | 0.0118615 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958055 | GCGTGTGGGAGCTGC[A/C/G]TGCACGCGTGTGGAG | 7468 |
rs188313141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891158 | CTTGGCCTCCCATAG[C/T]ACTGAGATTACAGGT | 7468 |
rs188361623 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941009 | CTTTACAGTTTGATA[A/C]GTGTAGATAATTAAG | 7468 |
rs188365311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971998 | CAGGACGCTCACGCC[A/G]CTCCTGTACCCCCAA | 7468 |
rs188395121 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949620 | ACAAAAAATTTAGCC[C/G]GACTTGTTGGCAGGT | 7468 |
rs188509279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945502 | CTAGTTCCAAAACCA[A/G]AAAAAGTGCCTGTGG | 7468 |
rs188511324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930463 | CACAGCATCAGTTAA[A/G]CACTACTTTTCTTTG | 7468 |
rs188529460 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966134 | AATTAAGACATTCCC[A/C]GATAAACAAAAGCTG | 7468 |
rs188529715 | snp | A/T | 0.078151 | 0.181571 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897504 | AAGGGAAAAAAAAAA[A/T]TGTTTGGCAGGGTAC | 7468 |
rs188541606 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880665 | CCTATGTTTAACAAC[C/T]AATCTACAGGAAATA | 7468 |
rs188545631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914992 | ATTTGGGTATCAAAC[C/T]TCCTAGATTGATCTT | 7468 |
rs188571774 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895311 | CACCCTGTTTTGTTC[A/G]ATGTTATAATCCCAA | 7468 |
rs188636828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1948935 | GGTTGGTGGATAGCG[C/T]TGGGGCTCTCTCCCC | 7468 |
rs188675749 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917095 | ATTTTTATTCTTTAA[A/G]TTAACTTATTTTTGT | 7468 |
rs188678942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900485 | AAAACTGCCTTCTGT[G/T]ACCTGAATTATTATA | 7468 |
rs188686813 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883452 | GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 7468 |
rs188689194 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917322 | GTATACACACACACA[C/G]ACAGAGGGATTAATG | 7468 |
rs188774715 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912511 | GAAATCATACACTAT[C/G]TTGTCCATACAGCCT | 7468 |
rs188782827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934211 | CTGCCTCAGCCTCCT[A/G]TGTAGCTGAGATTAC | 7468 |
rs188796481 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973821 | ACACGTGACTGTTAC[A/G]CTTTATGTGGCCTTT | 7468 |
rs188821762 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880049 | AGTTTTTGGGTATTA[C/T]TCTGTTTTCCTAATG | 7468 |
rs188837738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878846 | GGCAAGGCTGGGAAG[A/G]TGTGGACAGGTGGGA | 7468 |
rs188847710 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911849 | ATTTATTTTACAAAC[C/T]TGGGATCAGATTACA | 7468 |
rs188912453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932192 | CTGTAATCCCAGCAC[A/T]TTGGGAGGCCAAGGT | 7468 |
rs188918923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970812 | CATGCAGGCTGACGG[C/G]TCACATAAAGGGCCG | 7468 |
rs188935057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899472 | TGGGGAACAAAATCC[G/T]CCCCATTTGAGAACC | 7468 |
rs188991855 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875075 | CAAGCTTTCCTCCCA[C/G]CTCATTCTCCTAAGT | 7468 |
rs189011763 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955398 | CCCAGGAGCCACATA[C/T]CAAGGCAGGCTCATT | 7468 |
rs189027904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977504 | AAAGAGGCCAGGTGC[A/G]GGGGCTCATGCCTGT | 7468 |
rs189050066 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935625 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATTG | 7468 |
rs189054462 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922230 | AAAACTCAAGAGAAT[A/G]TACAGAAAATCTTTT | 7468 |
rs189059638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932549 | GTCGGGAGTTTGAGA[A/C]CAGCCTGACCAGCAT | 7468 |
rs189063860 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952850 | CCCAAGGAGTCTCCT[A/C/G]TCTCACGTCAGAACA | 7468 |
rs189065442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949145 | CTGCTGAGTCCATAT[C/T]TGATGCGCTTGTTAA | 7468 |
rs189066047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896150 | AGCTCCACACTTGGT[A/G]CTCCTAATCACGGCA | 7468 |
rs189094333 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920592 | GGTATATGTGATATT[C/T]GGTACGTGCATTAAA | 7468 |
rs189130731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975948 | ACAGAGATTTGGGGG[A/G]GCACTCTTGCACCCC | 7468 |
rs189164607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915482 | CTGTGTTCTCTTTTC[A/G]TAGCACACAGGGTTT | 7468 |
rs189166474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959195 | GGCCTGGCTGGATAC[A/G]TGTCAGCTCTTGTTC | 7468 |
rs189169651 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979826 | GTGTGTTTACTGATG[C/G/T]GGCCCTGAGCTCCAT | 7468 |
rs189184887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909234 | ACAACAAGATGTTCC[A/G]GGCTCATCTTGTACT | 7468 |
rs189193915 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902186 | CTCAGGAGCTGTTTA[C/G]TTCTCGCTCATGTAA | 7468 |
rs189200247 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939309 | GTTATATGTAAGACT[C/T]TATGTTTAGAGATTT | 7468 |
rs189200553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924390 | CCGTCAGCCACTCTG[G/T]TATGTTGCTCGGCTG | 7468 |
rs189206383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884277 | ATTTTTGTATTTCTT[A/G]TAGAGATGGGATTTT | 7468 |
rs189259380 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960896 | ATTTAATTTATGGAG[A/T]CTTTGTACACGCCCT | 7468 |
rs189276047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932781 | AATCCATACAGATGC[A/C]CCTGTTGCTTGTTTC | 7468 |
rs189318701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901744 | CCTTACCCTGTGGTC[C/T]AGTGTCCACTTACTG | 7468 |
rs189339752 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904990 | ACAAAATTAGCCGGA[C/T]GTGGTGGTGCACGCC | 7468 |
rs189343926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872103 | TTGTTTGCAGGCGGT[A/G]TCTGGCGTTGACACT | 7468 |
rs189344167 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888723 | GCGTGAACCCACTGC[A/G]CCTGGCTAATTTTTG | 7468 |
rs189407027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930521 | GTGGGAATAAAAATG[C/T]GACACACTAAGTTCT | 7468 |
rs189412943 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1954921 | CAGGTCGGCTGCCCA[C/T]GTGCCCCAGGTGCCT | 7468 |
rs189446747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887250 | CGTGGTGGCTGGTTC[C/T]ATGAGGGAGGAAGTG | 7468 |
rs189455238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897908 | CTGGGATTGCAGGCA[C/T]GAGCCACCTCACCCA | 7468 |
rs189509667 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981126 | CTTGTGATTTTTAAT[C/T]GCTTTGATAATACTT | 7468 |
rs189564917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918869 | ATACCGAGAACAGGC[C/T]AGGCACAGTGGCTCA | 7468 |
rs189586116 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883827 | AGCTGCCTAGATGGC[A/G]ATAAGAAGCGAGTGT | 7468 |
rs189589851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877003 | TTAGCTGGGCGTGGT[C/G]GTGGGTGCCTGTAAT | 7468 |
rs189631975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970478 | GAATCAGGTGAAGCT[C/T]CAGCAACAAGTTGGG | 7468 |
rs189735969 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869572 | AGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 7468 |
rs189772399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937451 | CTAAAAAATACATGA[C/T]CCTAGACACTCAGAA | 7468 |
rs189775599 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973592 | CCACATTCTGGTACC[A/G]TTTCTGGTTTTAAAG | 7468 |
rs189805238 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890329 | TTTGAGATGGCGTCT[C/T]GCTCTGTCGCCTAGG | 7468 |
rs189816319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923277 | GAGGATTGCTTGAGC[C/T]ACTGCACCACTTCAG | 7468 |
rs189820415 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906548 | CCGCAGCCCAACTTA[C/T]ATATCATTGCATCTT | 7468 |
rs189832360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874034 | TTCCTGGCTCTGCCC[A/T]GTCCTTTTTAGCTGG | 7468 |
rs189911684 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916314 | GAGTGCATTTAGTCA[G/T]CTAGCTAGCTTTTTT | 7468 |
rs189930933 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925768 | TTTATATATCTATAT[A/C]TATATTTTTTTTTGT | 7468 |
rs189932182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931203 | CAATCCTCCTGGTTT[C/T]GGCTGTAGTCTGCAC | 7468 |
rs189946613 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939940 | TCAGATTCATGAAAT[A/G]GACAAACAGTGCACT | 7468 |
rs189948230 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898654 | GACAGAGCGAGACTC[A/C]GTCTAAAAAAAAAAA | 7468 |
rs189954528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894148 | TTTTTGTAGAGACGG[C/T]GTCTTACTATGTTGG | 7468 |
rs189956084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881623 | GCTGGTCTTGAATTC[C/T]TCGACTCAAGCAGTC | 7468 |
rs189961687 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980230 | AGTTCTACAGAGTGA[C/G]ACCTATCTATCTGAG | 7468 |
rs189964016 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909286 | AACCCTAGCATCAGC[C/T]GTTTCTCAGAGAAGG | 7468 |
rs189967113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910162 | GCATTGTTGTAATTT[A/G]CAGCAGCAGAACCTG | 7468 |
rs189986131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877983 | GCAGGGAACCACGAT[A/T]ATGCCACTGCATTCC | 7468 |
rs190104262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964802 | AATTCAAAAACAACT[A/G]TGGGGAAAATAAGAA | 7468 |
rs190120782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896775 | TTCTTTCTTCTCTTT[C/T]TTTTCTTTTCTTTTC | 7468 |
rs190131285 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929945 | CCAGGATCAGACTTC[A/G]GTGTGTCTGCGGATC | 7468 |
rs190137524 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872678 | AATTGGATAAAGTTC[A/T]GGCCTGGCTCAGGAG | 7468 |
rs190208208 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960271 | TTATGTCAGAATTCT[G/T]ATGGTTATTTTTATG | 7468 |
rs190221977 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919350 | TTGTGTCCACTGGCA[A/C]TGAGGGTGTTGATTT | 7468 |
rs190226548 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893180 | TATGCATATTAAACT[C/G]TCAGGCCAGGCTCGG | 7468 |
rs190228594 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925501 | CCCCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 7468 |
rs190232230 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950492 | AGGAAGAAGAGAAAC[C/T]GAACGGTCAGCCTGT | 7468 |
rs190277473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892548 | ACCTCTGTTCCTGTC[C/T]CCCTTAGAAAACCAC | 7468 |
rs190285879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948131 | TCTGAGTAGAGAGTG[C/G]AGAAAGTATTTTCAG | 7468 |
rs190286075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970052 | GAGAAAGAAGGAATG[G/T]AGGAAAGAAAGAGAA | 7468 |
rs190336960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944809 | TTTCCTCAGTGTTCA[C/T]GCAAAAATTAAATGT | 7468 |
rs190378860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888863 | GAGCCACCACGCCTG[C/G]CTGCTTTATTATTTT | 7468 |
rs190382907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913663 | GTGGACACATGACTC[A/G]CTTGACCTTACCTAT | 7468 |
rs190403703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880221 | GCAAAGCATCTTCTT[C/T]TCATTGAATCCTCAC | 7468 |
rs190432487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973290 | GTGGCACTGGGCCCC[A/G]CTGGTAATGGTAGGA | 7468 |
rs190443845 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972675 | CAGCTAGGAGTGGGG[C/G]AGATGCATTTTATAA | 7468 |
rs190453404 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879042 | CTTATTTCCTTCCAG[A/G]AGGAAGCTCTGATCT | 7468 |
rs190455376 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919942 | GCCGTCTCAAAAAAA[A/C]AGGAAAAAAAGTCTG | 7468 |
rs190461645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902680 | CTGACCTCAAACGAT[G/T]TTCCTGCATCAGAGC | 7468 |
rs190463545 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933390 | GTGTCCTTCTGCAAG[A/G]TGTTTTTTTTCTTTG | 7468 |
rs190482455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932924 | CTGGCTTTGTGCTCA[C/T]GAACGGGTGTTCTGA | 7468 |
rs190495817 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884721 | CAAATTGTATGCTCT[A/G]TTTGTAGAAGACAAA | 7468 |
rs190534104 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875865 | AGTGAGCCAAGACTG[C/T]GCCACTGCACTCCAG | 7468 |
rs190598099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881331 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT | 7468 |
rs190612080 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898578 | GTGAGGCAGGAGAAT[A/T]GAACCCGGGAGGTGG | 7468 |
rs190662603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978388 | CGGCACAGCTCCTCT[C/T]AGTTGCCGAAACATA | 7468 |
rs190691608 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937795 | AGCGCTGCTCTAGTG[A/C]TATGGGGACAGGACA | 7468 |
rs190693823 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923625 | ATGCTGGTGAAACAT[A/C/T]ATTTATTACACCTGT | 7468 |
rs190709066 | snp | A/C | 0.000101254 | 0.00711454 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957888 | CTTGAAAGGTAGTTA[A/C]CTGTATTTACTAAAA | 7468 |
rs190729386 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977995 | AGCTGGTCGTGGTGG[C/T]GGGCGCCTGTAATCC | 7468 |
rs190764092 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880811 | GAGACTGGAGGAACA[A/T]GGACTAATTTTTATT | 7468 |
rs190845153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927025 | GTCTCTTGAAGTTGC[A/G]TTTAAGATGTTACCT | 7468 |
rs190847626 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920957 | GCAAGAGGATTGCTC[A/G]AGTCCAGAAGTTTAA | 7468 |
rs190853731 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941912 | GCAAAGTGTAGTGTT[A/G]TAAAAAACAGCCTGT | 7468 |
rs190855534 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961374 | GCACCCTGAGGCTCT[C/G]CTTGTCCGGGTGTGC | 7468 |
rs190858669 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903238 | GTATAGTGCTCTTGA[A/G]CAAGGCTAGAGATTC | 7468 |
rs190871065 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933815 | TGTTGAAATTAATCA[C/T]CTCTGTAGAATTTGC | 7468 |
rs190972441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957427 | TAGCTGGGACCATAC[A/G]CACCTGCCATCATGC | 7468 |
rs190985903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956855 | CTGTGTGACTGCAGG[C/T]GGGGACCCGCGTATT | 7468 |
rs191017495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889352 | GCATGCGCTTCCACA[C/T]CCAGCTAACTTTTTT | 7468 |
rs191027684 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922645 | AAATAGCAGTATTTG[A/G]CCAGGTGTGGTGGCT | 7468 |
rs191089321 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951885 | CTTCCTTTGCCATTG[C/G]TGAGGACTGGCCTCT | 7468 |
rs191124193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920402 | GAGCTGAAATCATGC[C/T]GCTGCACTCCAGCCT | 7468 |
rs191132712 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935953 | CTGGCATCAAAGTCC[A/C]TTAGAGATATGTGTT | 7468 |
rs191142077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885655 | TCCTTGAGCCTAGCT[C/G]CTCTTCATGGCTGTG | 7468 |
rs191157250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958709 | TATGTAAAGAAAGTG[A/C]TCTGTATTCATCTTT | 7468 |
rs191185272 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924212 | ATAAAGTAATCAGCA[A/G]TGTGTGTACAGCCAC | 7468 |
rs191189059 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909076 | TCCTCCCTAAAAAAA[A/G]AAGAGTTATATATTT | 7468 |
rs191195472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939093 | TACCTTCTCCAACTC[C/T]TAATTAAAAGGAAAA | 7468 |
rs191206771 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981606 | GGAAACTCTTCAGGC[A/G]CCTGAAGTGAGAACC | 7468 |
rs191231038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875781 | GGGCATGGTGGTGGA[C/T]GCCTGTAGTCCCAGC | 7468 |
rs191235708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935784 | GAGAATTGCTTGAAC[C/G]TGACAGGCAGAGGTT | 7468 |
rs191249555 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977851 | AAAATCCAGGCCAGG[C/T]ACGGTGGCTCATGCC | 7468 |
rs191255426 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906071 | ACCCTGTGACTCCCA[G/T]GTCATTTGTTTGTGT | 7468 |
rs191279552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873280 | AATACCAGAGTCTGG[A/C]CTCTGATTATAACAG | 7468 |
rs191316668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963575 | TTGCTTTTGATTAGT[A/C]AAAAAGAAATGCCAG | 7468 |
rs191338974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912401 | TAATTTTGACTATGT[A/G]AATATCATTCAGTGA | 7468 |
rs191347035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943244 | ATTCACAGTACCATG[C/T]GAGTAGCCCACAGTT | 7468 |
rs191368365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895747 | CAGGTTTCCCTGCAG[A/G]TCCTACCAGTGTCAC | 7468 |
rs191378992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879666 | GCTCTTGTGATGAGC[C/T]GTGCCCTGTCCCATG | 7468 |
rs191489406 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982636 | AAGCCCCCAGCCCTG[A/G]CCCACCCCGTCCTGA | 7468 |
rs191498015 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875233 | CAAAGTACTGGGATT[A/G]CAAGTGTGAACCACT | 7468 |
rs191514428 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911920 | GCATTTATCTGTGTC[A/G]TTATTTATAAACATG | 7468 |
rs191529198 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942413 | TTAGAATGATGTAAT[A/G]TTCCAGGATGCTGCT | 7468 |
rs191633167 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968787 | TGGGGTGGAGGAGAC[A/C]CAGGAGACAGCATGG | 7468 |
rs191676987 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875076 | AAGCTTTCCTCCCAG[C/T]TCATTCTCCTAAGTA | 7468 |
rs191680070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907676 | CCAGGCTGGAGTGCA[C/G]TGGCACGATTTTGGC | 7468 |
rs191737778 | snp | A/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961829 | CACGGCAGGCTTTTG[A/G/T]CTTCTGGATGACTTC | 7468 |
rs191768591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927328 | GGGGCTTGAGCTCTA[G/T]GAGGCAGGGCTCACA | 7468 |
rs191811546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895507 | TGTGCCTGGTCTGCT[A/G]TATTCAACTCAACTG | 7468 |
rs191832403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894840 | AAAGCATTTAGTTCT[A/G]TGGTCTTAAGTGCAT | 7468 |
rs191901995 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932619 | GGCGTGGTGGCACAT[C/G]CCTGTAATCCCAGCT | 7468 |
rs191918314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949405 | TATCTAGTGAGAAGA[C/G]AAGAGTGGCTCACAT | 7468 |
rs191920733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971364 | ATTTAGGGCCTTCCC[A/G]CTGGCCTATGGGATC | 7468 |
rs191945846 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917594 | GGTGCCTGCCACCAC[A/G]CCTGGCTAATTTTTG | 7468 |
rs191956605 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890817 | TGGCCAGGCTGGTCT[C/G]GAACTCCTGACCTCA | 7468 |
rs191967820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915783 | TTTTCCTCTGGAGCA[C/T]TTCAGGTCTTCAGGA | 7468 |
rs191969432 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946627 | GGACTTTTTGTCAAC[A/G]AAATTGGTTTTGATC | 7468 |
rs192035024 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974132 | CTCACTGTCACTCGG[A/T]TCTGCATTTCTCCAC | 7468 |
rs192057086 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934577 | TTATAAGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 7468 |
rs192060792 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896990 | AGCCTCGGCAACATG[A/G]TGAGACTTTGTACAA | 7468 |
rs192073469 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953684 | GGTTTTCTTTGACAA[A/G]GGACCTGTCTCCCTT | 7468 |
rs192103195 | snp | A/G | 0.000131891 | 0.00811962 | missense | WHSC1 | GRCh38.p7 | 4:1904250 | CTTGTCCAAACACTG[A/G]AAGAGACAAAGACCA | 7468 |
rs192103903 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959255 | AATAATGTGAGGGGG[C/T]GTTGTGTTGCCCTGC | 7468 |
rs192109520 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979929 | CCCCGTAGGGCGCTG[C/T]AGGCCCCGGGGACCC | 7468 |
rs192119475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878376 | GCCTCCCAAAGTGTT[C/T]GGATTACAGGCGTAA | 7468 |
rs192128174 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952857 | AGTCTCCTATCTCAC[G/T]TCAGAACACTTCCTG | 7468 |
rs192129381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910350 | CCTGCCGCAGCCTCC[C/T]GAGTAGCTGGCACTA | 7468 |
rs192210777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899891 | AAAAATGTGACCTTA[C/G]TGCTGTGTTCTTTCT | 7468 |
rs192215466 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979267 | TCTGAAATGTGTAGC[A/G]TAGGCTTTTCCCAAG | 7468 |
rs192218125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883233 | TTCAGGTTCAGAAAC[A/T]AGAGAAAGCCCATTA | 7468 |
rs192223519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948234 | GCGGGAAACAACGGG[A/G]AAGTTCTTGACAGAG | 7468 |
rs192233515 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917129 | GAACTTATACTTGCT[C/T]GAAATATTGTAATGG | 7468 |
rs192263947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916481 | CTCCAGAGTAGCTGG[G/T]ACTACAGGTGCACAC | 7468 |
rs192283246 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882312 | GACACGTGCTTTATC[C/G]TGTTCCCTTTCTCTT | 7468 |
rs192348296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904051 | AGAGACAAAATTTTG[A/G]TGAAACGATGTTGAG | 7468 |
rs192355587 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886057 | CAAAATGTTGAAGCA[C/T]ATTTTCTGCTTATCT | 7468 |
rs192366322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935053 | ATGGGCTGGATCTGT[A/G]TGTTGAATGCCCTGG | 7468 |
rs192385991 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869970 | CAGCTGACTCCATTA[C/T]GTGGTCTATATCCGG | 7468 |
rs192388115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904801 | GAAGCTTGGGTAGAT[A/G]AATTGATTTTTACAT | 7468 |
rs192511968 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973873 | TGCGGTGGATCTGGC[A/G]GCTCCTCAGGTGGAG | 7468 |
rs192545197 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891181 | TTACAGGTGTGAGCC[A/G]CTGTGCCCCGCCTAC | 7468 |
rs192658185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963944 | TTAAGACTGCTGTGA[A/G]CTATGATCATGTCAA | 7468 |
rs192660217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944041 | AGCTGAATAACCAGG[A/G]GCACATGGGGGAACG | 7468 |
rs192661924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898878 | TCAAACTCTCCTCAG[C/T]CACACATTTCAAAAT | 7468 |
rs192671056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931795 | TTTAGAATAGCAAGG[A/T]TATTTAGGACTTGTA | 7468 |
rs192726449 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921746 | AAAATCACGCCAATG[C/T]ACTCCAGCCTGGGCA | 7468 |
rs192738902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954171 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCATCAT | 7468 |
rs192752841 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887550 | GCACGATCATAGCTC[A/G]CTGTAGCCTCCAACT | 7468 |
rs192793195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923722 | TCCTAGATATTTACC[A/C]TAGAGTAATTTTGCC | 7468 |
rs192801452 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958165 | TCTGTGGTGCCTGGC[A/G]TGGATGGCCACACAA | 7468 |
rs192821631 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908418 | GAGGCACAAGCAAAC[C/G]TACTTCAGAAGACTG | 7468 |
rs192842159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945233 | AACAAGACGGGGTGG[A/G]GTGGGGAGATGGGCA | 7468 |
rs192863283 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913860 | TCTACCATCTCTCGT[A/C]TCCACACACGAGGAG | 7468 |
rs192869304 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886708 | CCAGGCGTGGTGGCG[G/T]GCACCTGTAGTCCCA | 7468 |
rs192919821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932395 | AGTGAGGCAAGATCA[C/T]GCCACTGCACTCCAG | 7468 |
rs192927570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971129 | TTTGGGAGGCTGAGG[C/T]GGGTGGATTGCTTGA | 7468 |
rs192992535 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979092 | GCAGCGTCCGCTGCG[C/T]CTGCACTGATGACCG | 7468 |
rs193002981 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883705 | TCCCCATCTGCTCTC[C/T]CAGCTGTAGTGGAAG | 7468 |
rs193055064 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964821 | GGAAAATAAGAAAAT[A/T]TAGAAAATTAGACAG | 7468 |
rs193068091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930341 | GTGAGTTAGTGGTTT[C/T]GGAAAAGTATATATA | 7468 |
rs193149419 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896285 | CCCAGCACCTAAACC[C/G]TGGGGTCCTGCCATG | 7468 |
rs193150060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928701 | TAGCATTCATCCTAA[C/T]TGGGGGCTCTGGAGT | 7468 |
rs193163062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1948993 | GGGCCTTGGTTCCCC[C/T]ATCAGATGGGTCAGC | 7468 |
rs193208953 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880176 | GTTGGTGTAATCTTT[A/G]TAGAGCCTTGCTACA | 7468 |
rs193297882 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912932 | CCAGGTGCCAAGGCA[A/G]GAGACTGAAGGCACA | 7468 |
rs199564032 | snp | A/G | 4.95667e-05 | 0.00497804 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958042 | GCACATCAAGGTGGC[A/G]TGTGGGAGCTGCGTG | 7468 |
rs199570116 | snp | G/T | 0.000164799 | 0.00907592 | intron-variant, utr-variant-3-prime, missense | WHSC1 | GRCh38.p7 | 4:1942372 | CCAGTCAAGTTGGAT[G/T]TGAACCCAGCTGCTC | 7468 |
rs199570333 | snp | C/T | 0.00016503 | 0.00908228 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978699 | TTCGACTTCATTTTG[C/T]CACCTCTGCCCCAAT | 7468 |
rs199620695 | snp | C/G | 0.00160763 | 0.028306 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953561 | CTTGCTGTGGGTTCA[C/G]ATGCAGGCCAGACGC | 7468 |
rs199630463 | snp | C/T | 6.59098e-05 | 0.00574026 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959632 | GGTGTGTCCCGCGGG[C/T]GAGTTCTGCCAGAAC | 7468 |
rs199697623 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974227 | GTCTTTTTTTTTTTT[-/T]GAGACGGAGTTTTGC | 7468 |
rs199734752 | snp | C/G | 1.72597e-05 | 0.00293761 | missense | WHSC1 | GRCh38.p7 | 4:1900686 | AGCAGAGTCCCCTTT[C/G]TGTTCAGAGTGTTGT | 7468 |
rs199762353 | snp | A/C | 0.000264428 | 0.0114954 | missense | WHSC1 | GRCh38.p7 | 4:1918294 | AACCCTCAAGTAGCC[A/C]AGGAGGCTGGCATTG | 7468 |
rs199783576 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911375 | GGTGGGTGACTTGAG[A/G]TCAGGAGTTCGAGAC | 7468 |
rs199861312 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966372 | GCATGATTGAAGAGA[C/T]AGGGCTGGGCATGGT | 7468 |
rs199891295 | in-del | -/AG | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884134 | GGGTCTTGCTCTGTC[-/AG]ACCCAGGCTGGAGTG | 7468 |
rs199898258 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913014 | GACATAGAATATAGA[C/G]ATGATTATATATGAA | 7468 |
rs199918100 | snp | C/T | 0.000247107 | 0.0111127 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904281 | CCTGTTGAAATACAA[C/T]GTTGGTGATTTGGTG | 7468 |
rs199929737 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872593 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 7468 |
rs199937217 | snp | A/G | 6.59326e-05 | 0.00574125 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916956 | TGAGAAGAGCCTCGT[A/G]GCTTTTGAAGGAGAA | 7468 |
rs199956960 | snp | C/G/T | 0.000153988 | 0.00877328 | missense | WHSC1 | GRCh38.p7 | 4:1978831 | CACCAAGACTGAGAA[C/G/T]CCCCCCCCAGAGCCA | 7468 |
rs199968523 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887143 | TGTTGGTACTGGCTG[G/T]CAACTGTGAGAGTTC | 7468 |
rs200001444 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893221 | GCCTCCAATCCCAGC[A/C]CTTTGGGAGTCCGAG | 7468 |
rs200023148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913229 | CTTGGACTAGCGGTA[A/G]CGCCAGTGCCTGGGA | 7468 |
rs200043274 | in-del | -/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915458 | AATTTCAAATATCTC[-/TT]TGTTTTTCTGTGTTC | 7468 |
rs200107713 | snp | A/G | 0.000153709 | 0.00876533 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955378 | CGGCACACGCCTCTC[A/G]CACTCCCAGGAGCCA | 7468 |
rs200130380 | snp | A/G/T | 0.000362536 | 0.0134591 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975298 | TCTTCTCCCAGGGAC[A/G/T]GAGCTGACTTTTAAC | 7468 |
rs200279117 | snp | A/C/G/T | 0.00156345 | 0.0279225 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975427 | GCGCCCTCCTTCCCC[A/C/G/T]CAGGCTCTGTGTTGG | 7468 |
rs200311175 | snp | C/T | 1.66749e-05 | 0.00288741 | missense | WHSC1 | GRCh38.p7 | 4:1956120 | AGGCGCGAGTGTTCC[C/T]GTACATGGAGGGGGA | 7468 |
rs200313606 | snp | C/G | 3.31181e-05 | 0.00406914 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918254 | CAAGTTCACCTTTCT[C/G]TATGTGGGGGACCAG | 7468 |
rs200319561 | snp | C/G | 0.000131913 | 0.00812029 | missense | WHSC1 | GRCh38.p7 | 4:1900995 | GGACACCCCCTAACA[C/G]TACCCCTATCAAAAA | 7468 |
rs200322983 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906413 | TGGCTAATTTTTGTG[-/T]TTTTTTTTGTAGAGA | 7468 |
rs200335399 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964918 | GGTTGATCCTCTGCA[A/C]AGAAACAGCCTGCAA | 7468 |
rs200338583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925023 | ATGGGGCCTCCCTTC[C/T]CTCCCCTGGACTCTG | 7468 |
rs200343529 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970454 | GAGATGAGCTCCAGG[A/C]CTCCAGCAGAATCAG | 7468 |
rs200357368 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873799 | AGCAAGAACTTAAAA[A/G]AAGTGCTAAGATGGT | 7468 |
rs200364408 | snp | C/T | 1.76693e-05 | 0.00297226 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978602 | AAGTCGTGATTCCAT[C/T]ACTTCTGTGTGCTCA | 7468 |
rs200378025 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957376 | GCAACCTCCACCTCC[-/TG]GGTTCAAGCAATTCT | 7468 |
rs200401371 | snp | C/T | 0.000105718 | 0.00726964 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974698 | TGTGAGCAAGAGAAA[C/T]AGGACTGGTTTGGGG | 7468 |
rs200403135 | in-del | -/TATTAGTG | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893023 | GAGGAATTCTTAGGT[-/TATTAGTG]TATTAGTCTTCTTCC | 7468 |
rs200415868 | snp | C/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953341 | ATTCACTCATGTTTC[C/G]TGTGTAAAGAGAGCA | 7468 |
rs200512366 | snp | A/G | 0.000922357 | 0.0214553 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959629 | GCAGGTGTGTCCCGC[A/G]GGCGAGTTCTGCCAG | 7468 |
rs200531379 | snp | C/T | 0.00204239 | 0.0318908 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951223 | GGAGAAGGCAGCATC[C/T]GCTATGTCCGTGCTG | 7468 |
rs200573658 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916152 | TAGCACTGTGAGATA[-/G]GGGGGTAGCTAGCTG | 7468 |
rs200573697 | snp | A/G | 0.00199802 | 0.0315439 | missense | WHSC1 | GRCh38.p7 | 4:1918607 | TTTTGGTCTTCTGTC[A/G]AAAACACAGGGATGA | 7468 |
rs200582438 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876812 | ACTTGAGTTGGCACT[C/G]AGAGAGTTGATGATG | 7468 |
rs200604665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886338 | CAGTCTCCTGAATAG[A/C]TGGTATTACAGGTGT | 7468 |
rs200615147 | snp | C/T | 0.000618 | 0.0175675 | missense | WHSC1 | GRCh38.p7 | 4:1978803 | ATGACTTAGGGGCGG[C/T]ATCGGTCAGAAGCAC | 7468 |
rs200621548 | snp | C/G | 0.00199792 | 0.0315431 | missense | WHSC1 | GRCh38.p7 | 4:1900885 | CTTTATTCCAGCCGA[C/G]AAGCTGAAAGATCTT | 7468 |
rs200634771 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945033 | CTGTGTGTGATGTGC[A/G]GAGTCCTTGGACAGG | 7468 |
rs200636191 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975483 | TCCCCCGTGAACAGC[A/G]GCTTCCTCCAGGCTG | 7468 |
rs200642264 | in-del | -/CGT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914306 | AGATTACATGTGTGA[-/CGT]GCCACTGCACCCAGC | 7468 |
rs200689866 | snp | C/T | 0.00055992 | 0.0167226 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953346 | CTCATGTTTCGTGTG[C/T]AAAGAGAGCAAGACA | 7468 |
rs200692724 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911608 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAGAAA | 7468 |
rs200698192 | in-del | -/GAG | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949403 | TGTATCTAGTGAGAA[-/GAG]AAGAGTGGCTCACAT | 7468 |
rs200710940 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879374 | CAGGCGCCCGCCACC[A/C]TGCCCGGCTAATTTT | 7468 |
rs200712844 | snp | G/T | 3.59615e-05 | 0.00424022 | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1900642 | GTTCTAAGAACGGAA[G/T]CATCTGGGCTGGATG | 7468 |
rs200743149 | in-del | -/TTG | 0.0103295 | 0.0711199 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908776 | CCAACAGTGTAGCTT[-/TTG]TTGTTGTTGTTTTGA | 7468 |
rs200756781 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885129 | AAAAAAAAATAAAAA[-/T]AAAAAAAATAAAATT | 7468 |
rs200772900 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906654 | CTTCTCTCTCTCTCT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs200784805 | snp | C/T | 0.000334499 | 0.0129282 | missense | WHSC1 | GRCh38.p7 | 4:1918490 | GTACTCCTCAAAAGA[C/T]GGCAGAGGCTGACCC | 7468 |
rs200886469 | snp | A/G | 0.0022171 | 0.033221 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953122 | GAAGCTGGAGCTCAG[A/G]TCGCAGCAAGGTAAT | 7468 |
rs200891909 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928962 | GAGGGGTGTGGCAGG[C/T]GTAGGCATATGCAGG | 7468 |
rs200903511 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888929 | TTTTGAGACAGTCTC[A/T]CTCTGTTGGCCAGGG | 7468 |
rs200930154 | in-del | -/C | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889275 | AATTATGGCTCACAG[-/C]CTCTACCTCTTGGGC | 7468 |
rs200930259 | snp | C/G | 0.000229331 | 0.0107058 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959432 | GGTATTCGGAAGGCT[C/G]TCATGTGTGGACCAA | 7468 |
rs200939716 | snp | A/G | 1.82951e-05 | 0.00302443 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901259 | ATAAAAAGGTATTTA[A/G]GAGACGTTGTGTAAG | 7468 |
rs200955966 | snp | C/G/T | 0.000218473 | 0.0104495 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951023 | CAGGGCATGGCCACC[C/G/T]GCTGTGTTCTGCGAC | 7468 |
rs201018072 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937893 | TGCTTTTCTCAGTTG[G/T]GACATGTTTTACTGA | 7468 |
rs201071008 | in-del | -/AATTAA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923825 | GTGTAACTACACATC[-/AATTAA]AGTGAACTCATTGGA | 7468 |
rs201085081 | snp | C/T | 0.0007139 | 0.0188796 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955940 | AAATTATTATCGCTG[C/T]CTCTGAGGAGTCTGT | 7468 |
rs201126604 | snp | A/G/T | 0.000132396 | 0.00813524 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938547 | GGTAATGTGGTCAGC[A/G/T]CCCTTTCCTTCTTGG | 7468 |
rs201138525 | snp | A/C/T | 3.36707e-05 | 0.00410298 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961175 | GAACTCCACTGTGAG[A/C/T]TTCTGCAGTGTGCTG | 7468 |
rs201148179 | snp | C/T | 0.000214696 | 0.0103587 | missense | WHSC1 | GRCh38.p7 | 4:1978874 | GGGAAGAGGCGGCGG[C/T]GGAGGGGCTGGCGGA | 7468 |
rs201150147 | snp | C/T | 0.000252145 | 0.0112254 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952088 | CGGGCGCTGCTTACC[C/T]GCCTGCTCTGCCCCC | 7468 |
rs201159043 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913472 | AGCGGTCACGCTCCT[A/G]GTCCACTTTCATGTT | 7468 |
rs201163406 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942004 | ACACTGACACACACC[A/C]ATTGGGTCACACCCC | 7468 |
rs201168727 | snp | A/G | 0.00199798 | 0.0315436 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901312 | GAGCATGGCCACCCT[A/G]TGAGGGCACCTGCAC | 7468 |
rs201194790 | snp | C/T | 0.000104767 | 0.00723688 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976678 | TGGCAAGCGGCCCTT[C/T]GGTGGGTGTGCAGCC | 7468 |
rs201203687 | snp | C/T | 1.6755e-05 | 0.00289435 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918173 | AGGGAAATTGAGGGC[C/T]CAGTGGGAAATGGGC | 7468 |
rs201208580 | snp | A/G | 1.67231e-05 | 0.00289159 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952250 | AGTTCCCACGGGCGG[A/G]CAGCTCTGCAGCCTG | 7468 |
rs201209975 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913096 | ATCTCTGTTCTACAA[C/T]TATAACCTAGGAAAA | 7468 |
rs201210085 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897132 | CATGATCATACCACT[-/G]GCACTCCAGCCTGGG | 7468 |
rs201242554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895716 | GGGGAGAGGGGGGCT[C/T]CCCATGAGCAGTTCT | 7468 |
rs201252361 | snp | C/T | 9.88728e-05 | 0.00703041 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951100 | CGGGAGACGAGCCCT[C/T]GGAGTCCCCATACGA | 7468 |
rs201271995 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943726 | AAAATTAAAATTCTC[-/A]AAAAAAAAACCCCAC | 7468 |
rs201317633 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873802 | AAGAACTTAAAAGAA[G/T]TGCTAAGATGGTGCT | 7468 |
rs201351189 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905139 | CTGTCTCACAAAAAA[A/G]AAAAGAATGTTATAT | 7468 |
rs201356947 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966373 | CATGATTGAAGAGAT[A/G]GGGCTGGGCATGGTG | 7468 |
rs201357803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926416 | CCTCAGCCTCCCAAA[A/G]TGCTGCGATTACAGG | 7468 |
rs201402470 | snp | C/T | 8.29896e-05 | 0.00644111 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918455 | AGAGACCCTGGAGAG[C/T]CACCCCGACATAGGG | 7468 |
rs201445414 | snp | C/G | 5.27347e-05 | 0.00513465 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974706 | AGAGAAACAGGACTG[C/G]TTTGGGGGTGTCCTG | 7468 |
rs201455479 | snp | C/T | 6.62745e-05 | 0.00575612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958060 | TGGGAGCTGCGTGCA[C/T]GCGTGTGGAGGGAGT | 7468 |
rs201461316 | in-del | -/TGAAGAG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966364 | TGTTGTCTGCATGAT[-/TGAAGAG]ATAGGGCTGGGCATG | 7468 |
rs201476741 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930076 | CCCTGGTGTGGCTGG[C/T]GGGTAGGGAAGCCTC | 7468 |
rs201485659 | in-del | -/GTG | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886997 | AACATTCCCAATATT[-/GTG]GTGGTTTGATGATCT | 7468 |
rs201509574 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923683 | GAAATTGAAGATGTG[-/C]CTTTTTTTCTCTTAC | 7468 |
rs201513781 | snp | C/T | 0.000261904 | 0.0114404 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976573 | GAGGCAGTCAGAGGA[C/T]GAGTGCTTCCGCTGC | 7468 |
rs201530243 | snp | C/G/T | 8.2417e-05 | 0.00641892 | missense | WHSC1 | GRCh38.p7 | 4:1975297 | CTCTTCTCCCAGGGA[C/G/T]GGAGCTGACTTTTAA | 7468 |
rs201550176 | in-del | -/GCAGGCTTTTGGCT | 0.00993419 | 0.0697739 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961818 | CCCTTCCCTCACACG[-/GCAGGCTTTTGGCT]TCTGGATGACTTCAG | 7468 |
rs201573732 | snp | C/T | 1.64909e-05 | 0.00287144 | missense | WHSC1 | GRCh38.p7 | 4:1900907 | AAAGATCTTACTTCC[C/T]GGGTGTTTAATGGAG | 7468 |
rs201587740 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893343 | GGCGTGGTGATGCAT[A/G]CCTGTAGTCTCAGCT | 7468 |
rs201612782 | snp | C/T | 0.000115334 | 0.00759299 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904270 | GACAAAGACCACCTG[C/T]TGAAATACAACGTTG | 7468 |
rs201619712 | snp | A/C/G/T | 0.000305784 | 0.0123621 | missense | WHSC1 | GRCh38.p7 | 4:1978836 | AGACTGAGAAGCCCC[A/C/G/T]CCCAGAGCCAGGGAA | 7468 |
rs201632775 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932724 | GGATTCCAGCCAATG[A/G]AATGGCCAACAGGAG | 7468 |
rs201639781 | snp | A/T | 0.000399281 | 0.0141238 | missense | WHSC1 | GRCh38.p7 | 4:1935201 | AGGACCCTACAGAAG[A/T]TGCTGAAGCTGAGGA | 7468 |
rs201661271 | snp | A/C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940470 | ATTTTTTGCCGTTGC[A/C/T]AAAAACAACAAATAG | 7468 |
rs201695295 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959437 | TCGGAAGGCTCTCAT[A/G]TGTGGACCAAGACAG | 7468 |
rs201750568 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912952 | CTGAAGGCACAGGCT[C/G]TTCCAGTATAATAAA | 7468 |
rs201785293 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935860 | GCAAGATTCTGTCTC[-/A]AAAAAAAAACAAACA | 7468 |
rs201827731 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927719 | GAGACTCTTATCTCA[A/G]AAAAAAAAAAAAAAA | 7468 |
rs201849959 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974675 | CCACGTGGTCCTGAC[C/T]TGTCCTCTGTGAGCA | 7468 |
rs201854092 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957293 | TTTGTTTTTGTTTTT[-/G]TTTTTTTTGAGACTG | 7468 |
rs201865049 | snp | C/T | 0.00199798 | 0.0315436 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956064 | GATTGGAGAATTCCC[C/T]GTGTTTTTCTTTGGG | 7468 |
rs201890475 | in-del | -/AG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917325 | TACACACACACAGAC[-/AG]AGGGATTAATGTAAT | 7468 |
rs201937275 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875751 | ACTAAAAAAAAAAAA[A/T]ACAAAAAATTAGCTG | 7468 |
rs201940467 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943315 | AACGTTTCTGACTAA[C/T]ATTTTGTTGTAAACC | 7468 |
rs201941821 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913500 | GTTCCGCCCTGTACA[C/T]CTGGCTCCGCCTTCT | 7468 |
rs201950005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922708 | AGGCAGGCGGATCAC[C/T]GGAGGTCAGGAGCTC | 7468 |
rs201961899 | snp | A/G/T | 0.000329744 | 0.0128364 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955678 | AAGCCTGGCCGCCTC[A/G/T]CCCTCCTCTTGCAGG | 7468 |
rs201970252 | snp | C/T | 5.00513e-05 | 0.00500231 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952243 | TCAGGCAAGTTCCCA[C/T]GGGCGGGCAGCTCTG | 7468 |
rs201986259 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957301 | TGTTTTTTTTTTTTT[-/T]GAGACTGAGTCTTGC | 7468 |
rs202006784 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913113 | ATAACCTAGGAAAAA[C/T]CAGGTCATACAGAGA | 7468 |
rs202031644 | in-del | -/ACCCA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907854 | TTGACCTTGTGATCC[-/ACCCA]CCTTGGCCTCCCAAT | 7468 |
rs202034076 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893560 | TTTTTTTTTTTTTTT[G/T]TTTTGTTTTGAGACA | 7468 |
rs202059983 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907615 | CTACCTGTTGAATCT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs202069262 | in-del | -/GAGT | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982164 | AAATTGTGTATGAGT[-/GAGT]ATTTTTGTATTAAAA | 7468 |
rs202078054 | snp | A/G | 0.000933613 | 0.0215855 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959781 | CTTTTGAGAAATTAC[A/G]GTTCACTGGGTAATT | 7468 |
rs202081447 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955113 | GCTCTTTTCACTATG[A/T]CTGGAGTCAGTGTTT | 7468 |
rs202141910 | snp | C/T | 0.000596758 | 0.0172633 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959759 | TGTGTCGTTATCCCC[C/T]CCCCTGCTTTTGAGA | 7468 |
rs202200306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964671 | TCAGTCGTTACAAGC[C/T]CCTCCCCCTCCAGCT | 7468 |
rs202207779 | snp | C/T | 0.000298349 | 0.0122101 | missense | WHSC1 | GRCh38.p7 | 4:1917014 | AGTGCCAAGCAGGCA[C/T]CCACGAAAGCTGAGA | 7468 |
rs202228817 | snp | G/T | 8.0331e-05 | 0.00633712 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976439 | TTCAGCCTGTGTAAT[G/T]CTTTCCGGTGATCTG | 7468 |
rs202230841 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898273 | GTATTTTTTGTTGAG[-/A]ATGGGCTCTCACTGT | 7468 |
rs202235551 | snp | A/G | 0.00046162 | 0.0151854 | missense | WHSC1 | GRCh38.p7 | 4:1900853 | ATGCAGAAGTTTAAC[A/G]GCCACGACGCCCTGC | 7468 |
rs202245225 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955806 | AGGGCTGGGAAGAAG[C/T]TGCACTTCCAGGATA | 7468 |
rs207464228 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949473 | AGCCCTTGGAAAAAG[C/T]CCACTCTGGCTGGGT | 7468 |
rs267600117 | snp | C/T | | | missense | WHSC1 | GRCh38.p7 | 4:1918460 | CCCTGGAGAGTCACC[C/T]CGACATAGGGAAGAG | 7468 |
rs267600121 | snp | C/T | | | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956061 | CGAGATTGGAGAATT[C/T]CCTGTGTTTTTCTTT | 7468 |
rs367568269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977668 | GTAATCCCAGCTATT[C/T]GGGAGGCTGAGGCAG | 7468 |
rs367594911 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905707 | CTTGCCTGAGTCCTG[C/T]CCTGGCCTCCTGTCC | 7468 |
rs367599593 | in-del | -/ATATATATATA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878241 | GATATATATATATAT[-/ATATATATATA]TTTTTTTTTTTTTTT | 7468 |
rs367649140 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944056 | GGCACATGGGGGAAC[A/G]TGGATGGGAATGATA | 7468 |
rs367656377 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938576 | GGCTTCTGGGTGCCC[A/G]GGCTGGGCTGGGTGG | 7468 |
rs367660898 | snp | A/G | | | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975202 | AGATACAAAAATAAT[A/G]AGAGTATTTTTGTTG | 7468 |
rs367666671 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884458 | GAGTGCAGTGGCCCA[A/G]TCTTGGCTCACTGCA | 7468 |
rs367675002 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915641 | TCGTGTTTAAGAGCA[C/T]GACACTTAGAGCTGC | 7468 |
rs367675547 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879511 | GGCTTGAGCCACCGC[A/G]CCTGGCCTACACACA | 7468 |
rs367692823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897022 | AACACAAAAATTAGC[C/T]GGGCATGGTGGCAAG | 7468 |
rs367695251 | in-del | -/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974384 | CCAGCTAATTTTTTT[-/G]TGTATTTTTAGTAGA | 7468 |
rs367742185 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972185 | CCTCCTCATGTATGC[A/G]GAGCCACAAAGAGCA | 7468 |
rs367762473 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949610 | TACTAAAAATACAAA[A/C]AATTTAGCCGGACTT | 7468 |
rs367770508 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923742 | GTAATTTTGCCCTTG[A/C]ACGCAGAGAGACCAC | 7468 |
rs367774341 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876717 | AAACACAAAACCCCA[A/G]TAGTGAGACTACCCT | 7468 |
rs367785336 | snp | A/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980708 | GTCCCCAGCAAAGTT[A/T]ACTACACAGAGGACC | 7468 |
rs367816556 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886688 | ACACACACCCAAAAA[-/A]TTAGCCAGGCGTGGT | 7468 |
rs367854444 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924282 | TGAATGGACACTCCA[C/G]TGTTTGACAGCTAGG | 7468 |
rs367914017 | snp | A/G/T | 5.7982e-05 | 0.00538407 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976492 | CTCGACGACCCTTTC[A/G/T]TCAGAGGAAAAGGGC | 7468 |
rs367940341 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897173 | AGACTCTGTCTCAAA[A/G]GAAAAAAAAAAAAGG | 7468 |
rs367943032 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955350 | CCAAAGGTGAGGGGC[C/G]TGGGGGTGTCTGCGG | 7468 |
rs367950286 | snp | A/C | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952434 | TGCTCTGATTTCAGT[A/C]GTATGTGCCCCCTTG | 7468 |
rs368035388 | snp | C/T | 0.000131911 | 0.00812022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975287 | TGTCTGTCTCCTCTT[C/T]TCCCAGGGACGGAGC | 7468 |
rs368066148 | snp | C/T | 3.34096e-05 | 0.00408702 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952101 | CCCGCCTGCTCTGCC[C/T]CCGCAGCTGTGTGAG | 7468 |
rs368125048 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908006 | GACTCAGCACCAGCC[A/G]CATTTCGGGAAACAT | 7468 |
rs368166556 | snp | A/G | 0.000354431 | 0.0133075 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976432 | TATTTGCTTCAGCCT[A/G]TGTAATTCTTTCCGG | 7468 |
rs368230365 | snp | A/G | 3.37041e-05 | 0.00410498 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961000 | AGGATTGGTCAGCAC[A/G]CTTTTTGTCATGGCC | 7468 |
rs368232446 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1930640 | GGTGGTAGCTGAGCA[C/T]CCAGATGCTTCAGGT | 7468 |
rs368243950 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967446 | AGCTGGGCGTGGTGG[C/T]GGGCGCCCATAATCC | 7468 |
rs368246985 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892631 | AGTGTAGTGGCCTGA[G/T]CTCGGCTCGGCTCAT | 7468 |
rs368262319 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933836 | TAGAATTTGCACTTA[C/T]ACCTTACCGTCTTAG | 7468 |
rs368298262 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939928 | CTCTTGGCTAACTCA[C/G]ATTCATGAAATGGAC | 7468 |
rs368311101 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927800 | TGTAATCTGAAGACT[C/G]TAATTTGTAGAGTCT | 7468 |
rs368313644 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969202 | AGAAGAGATGACACA[C/T]CTTTGAAAGGATCAC | 7468 |
rs368316611 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924392 | GTCAGCCACTCTGGT[A/G]TGTTGCTCGGCTGTG | 7468 |
rs368325872 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929270 | GTGGTGACTGTCTTG[A/G]GAGGAGGGGTTTGGG | 7468 |
rs368336519 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898137 | TGTAATCCAGGTTGG[A/T]GTGCAGTAGTGCAAT | 7468 |
rs368337765 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914243 | GGCCAGGCTGGTCTC[A/G]AACTTCTGACCTCAA | 7468 |
rs368339806 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874260 | CTTGTTTTGCTTGAT[C/T]GTAGTAAGTGTGACC | 7468 |
rs368384180 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975912 | TTCCAAATACAGTCA[A/C]CTTCCAAGGTTCCAG | 7468 |
rs368387237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952954 | AGTGTCTGTCTGCCT[A/G]CCCAGAATGATAAGT | 7468 |
rs368388846 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923225 | AGGCATGGTGACTCA[-/A]CGCCTGTAATCCCAG | 7468 |
rs368391105 | in-del | -/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870843 | CGGGGCCTCTGCGGC[-/G]GGTTTCCCCACCCGT | 7468 |
rs368415729 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929470 | GAACTACCCAGTAGA[A/G]GAGCCAGCATCAGAG | 7468 |
rs368418997 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898690 | AAACAAAAAACACAC[-/T]TTTTTTTTTTTTTTT | 7468 |
rs368430615 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971216 | AAAAATTGTGGCCAA[A/C]GGTATGCCAAGGTGA | 7468 |
rs368458555 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911608 | AAAAAAAAAAAAAAA[-/G]AAAAAAAAAAAGAAA | 7468 |
rs368480260 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908618 | TGAGGGAAGGACAGA[A/G]TGCTAGTCAGACCAC | 7468 |
rs368545003 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882272 | CATTGGAAAGTGACA[C/T]GTAACTTCTGAGTGG | 7468 |
rs368548857 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964085 | GAGCAGACCTTCCTA[A/G]TGGAAGGCTTTGCTT | 7468 |
rs368628697 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941870 | GTTTGTGATGTTTCC[A/G]ATGCTGAATGCCTGT | 7468 |
rs368713582 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914638 | GCCCAGAGTATGCTA[C/G]TTTTCTATCTTCACA | 7468 |
rs368725595 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977700 | AGAAATGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 7468 |
rs368733460 | in-del | -/GGT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887002 | TCCCAATATTGTGGT[-/GGT]TTGATGATCTATTCC | 7468 |
rs368737664 | snp | A/G/T | 0.000437904 | 0.0147905 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948503 | GTTGCCGAGCCGAGA[A/G/T]CATTGGATCCTCCCC | 7468 |
rs368751284 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920597 | ATGTGATATTTGGTA[A/C/T]GTGCATTAAAGTTCA | 7468 |
rs368774033 | snp | C/G/T | 0.0002021 | 0.0100504 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952268 | GCTCTGCAGCCTGGC[C/G/T]GGCCACCTGCTCCTG | 7468 |
rs368796161 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936504 | GGTGAAACCCCATCT[C/T]TACTAATAATACAAA | 7468 |
rs368796245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965402 | ACCAAGCAGACCAAT[A/G]TATCTATTGTGGGAG | 7468 |
rs368799821 | snp | A/C/G | 9.1048e-05 | 0.00674661 | missense | WHSC1 | GRCh38.p7 | 4:1978839 | CTGAGAAGCCCCCCC[A/C/G]AGAGCCAGGGAAGCC | 7468 |
rs368817154 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980133 | AGGTGTGCGTGCCTC[A/G]TACGTGTGTTATGGG | 7468 |
rs368822409 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885007 | CTCAGCTACTCAGGA[A/G]GCCGAGGCAGGAGAA | 7468 |
rs368834275 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930887 | CCTGTTTCTGACCCG[C/T]GGGGTTTGGGCCAGC | 7468 |
rs368860271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955506 | AATTAATTGTAATCA[C/T]TTCGCAAACATACAG | 7468 |
rs368865778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924676 | AGCACCTTGGGAGGC[C/T]GAGGAGGGTAGGATG | 7468 |
rs368924226 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926295 | GAGTAGCTGGGATTA[C/T]AGGTGCCCACCACCA | 7468 |
rs368953029 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929847 | CACTGAGGCCAGACC[C/T]GGTGGGTTGGGTTGA | 7468 |
rs368955180 | snp | A/C | 5.3845e-05 | 0.00518841 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953565 | CTGTGGGTTCAGATG[A/C]AGGCCAGACGCAGGC | 7468 |
rs368977435 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977415 | CAATCTTGCAGTGTG[A/T]CGCCATGAGGCTCTT | 7468 |
rs368994155 | in-del | -/TCTTG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937551 | AAAGAAGTAATGGTG[-/TCTTG]TCTCTTCAGATTTGG | 7468 |
rs369016670 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912239 | CTTCTACTTCTAATA[C/G]TTTGATTTCTCATGT | 7468 |
rs369022640 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970921 | TAGAAACAAGCAAGA[A/C]ATGAATGTGTTCTGA | 7468 |
rs369031555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965941 | TACAATTCAAGATGC[A/G]ATTTGGGTGGGGACA | 7468 |
rs369062153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898568 | ACTCAGGAGGGTGAG[A/G]CAGGAGAATTGAACC | 7468 |
rs369065442 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962274 | AAGGACAAAAAGAAT[C/T]CTGGGTTAAAAGAGA | 7468 |
rs369088750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909928 | ACAGGCGTGAGTCAC[C/T]GCGCCCGGCACCCGT | 7468 |
rs369094840 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899543 | CAGATTTTCCCTAGT[A/G]TCTGATGCTATTGAT | 7468 |
rs369098444 | snp | C/T | 1.85765e-05 | 0.00304761 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901293 | TCATGTGACCTTGAG[C/T]AGTGAGCATGGCCAC | 7468 |
rs369187883 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939126 | AAACCCTGGGGAGGA[C/G]AGTGGCAATGGCTCT | 7468 |
rs369193587 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910351 | CTGCCGCAGCCTCCC[A/G]AGTAGCTGGCACTAC | 7468 |
rs369198150 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880128 | GTGTTAGAAATAGGA[A/G]GCTTCTGTGTTCTTT | 7468 |
rs369307480 | snp | A/G | 1.71179e-05 | 0.00292552 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978822 | GGTCAGAAGCACCAA[A/G]ACTGAGAAGCCCCCC | 7468 |
rs369334773 | in-del | -/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869531 | TTTTGTATTTTTTTT[-/T]AGTAGAGACGGGGTT | 7468 |
rs369361984 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904112 | CTCCATTTTTGGGGG[-/G]TCTGTGTGTATTTGG | 7468 |
rs369375527 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968775 | GTTTGTAGTTATTGG[G/T]GTGGAGGAGACACAG | 7468 |
rs369404968 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956687 | TTGAGGGAGGCAGGA[C/T]GGGGATGTGACCCTT | 7468 |
rs369437427 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894044 | TAAGTGATCCTCCTC[C/T]CTCAGCCTCTGAAGA | 7468 |
rs369447966 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878251 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 7468 |
rs369458743 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938169 | TGGCCCCACCCACCT[C/T]GCCCTCCTGACAGAT | 7468 |
rs369465574 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958047 | TCAAGGTGGCGTGTG[A/G]GAGCTGCGTGCACGC | 7468 |
rs369474320 | snp | C/T | 3.48979e-05 | 0.00417705 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974719 | TGGTTTGGGGGTGTC[C/T]TGTCTCAGTGGACAC | 7468 |
rs369527225 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974860 | TATCACTTGACCTTA[C/T]AGGACCGTATAATAG | 7468 |
rs369554721 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963075 | CCAAGAATACACAAC[A/G]AGAGAGAAAGAACAA | 7468 |
rs369561001 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930390 | TTTCCAACATTTACA[A/G]AAGTAGAGTTGAATT | 7468 |
rs369569430 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909078 | TCCCTAAAAAAAAAA[-/A]GAGTTATATATTTTA | 7468 |
rs369572952 | snp | A/G | 0.000165415 | 0.00909286 | missense | WHSC1 | GRCh38.p7 | 4:1955824 | CACTTCCAGGATATC[A/G]TTTGGGTGAAACTTG | 7468 |
rs369582553 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887912 | CAGTTCCTTTTTTTC[-/T]TTTTTTTTTCTTCTG | 7468 |
rs369609076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925840 | AGGGTCTTACTCTGT[C/T]GCCCAGGCTGGAGTG | 7468 |
rs369632306 | snp | A/G | 3.30759e-05 | 0.00406655 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918428 | GCGGAGGGCCAAACT[A/G]TGTAGCTCTGCAGAG | 7468 |
rs369690906 | snp | C/T | 3.3749e-05 | 0.00410772 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975420 | GGCTGTGGCGCCCTC[C/T]TTCCCCCCAGGCTCT | 7468 |
rs369731282 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877028 | TGTAATCCCAGCTAC[G/T]CGGGAGGCTGAGGCA | 7468 |
rs369741232 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894285 | TGTCCTCCATGTTCT[A/G]TCATTTCAATACAAT | 7468 |
rs369754551 | snp | C/T | 0.000108614 | 0.00736853 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976588 | CGAGTGCTTCCGCTG[C/T]GGTGATGGCGGGCAG | 7468 |
rs369768860 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960362 | CACTCACCAGCAGGC[A/G]TAAGGAGATTGCTCT | 7468 |
rs369788792 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893565 | TTTTTTTTTTGTTTT[G/T]TTTTGAGACAAGGTC | 7468 |
rs369805993 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905143 | TCACAAAAAAAAAAA[-/A]GAATGTTATATGTCC | 7468 |
rs369816995 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910996 | GCATCTTTATGGCTT[C/T]TCTTCCCTCCCTGGA | 7468 |
rs369823040 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946066 | TAGATTCATCACCTT[A/C]GTTTTTTAAAAAAAA | 7468 |
rs369908118 | snp | A/G | 3.37388e-05 | 0.0041071 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939632 | ATGATTTGAAACTTT[A/G]CAAACCAAAATTATT | 7468 |
rs369960570 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932239 | GCCAGGAATTCAAGA[A/C]CAGCCTGGCCAACAT | 7468 |
rs369989628 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930266 | ATGTTCAGGGGCAGC[A/G]TTCCTGTGGCACTGG | 7468 |
rs369991547 | snp | A/G | 3.31524e-05 | 0.00407125 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952219 | AGGTTCACCTGCAGC[A/G]AGTGTGCCTCAGGCA | 7468 |
rs370017398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945113 | TGCTTAGAGGATCTC[C/T]GAGAGGTCCCCGCAG | 7468 |
rs370031459 | snp | A/G/T | 0.000108324 | 0.00735884 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953575 | AGATGCAGGCCAGAC[A/G/T]CAGGCCCATGGGCGC | 7468 |
rs370035048 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950313 | AAGAGATACAACCTG[C/T]GAGCAATTCCACTCG | 7468 |
rs370039362 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923971 | ATCTAAAAAGTGTAA[G/T]TGGGCAGCTGTGAAG | 7468 |
rs370043407 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978951 | AGGGGCGGTGCAGGG[C/T]GGCCGGCCCTGCCTG | 7468 |
rs370045092 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946994 | CCATCCAGGCATATA[A/G]TATTTTCAAGAAATG | 7468 |
rs370075112 | snp | A/G | 6.60971e-05 | 0.00574841 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959747 | ATCAGAAAGGTATGT[A/G]TCGTTATCCCCTCCC | 7468 |
rs370081070 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891050 | AGGCACATGCCACCA[C/T]GCCCAGCTAAGTTTT | 7468 |
rs370089941 | snp | C/T | 0.000155988 | 0.00883004 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900615 | CTTTTTTCTTTTTTT[C/T]AATACCATAGTGTTC | 7468 |
rs370107372 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932480 | AGCCCGGCGCAGTGG[C/T]TCCCGCCTGTAATCC | 7468 |
rs370122974 | snp | A/T | 5.00705e-05 | 0.00500327 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974802 | TATGATGGTGAAAAT[A/T]CCCTTTAAAAATAAC | 7468 |
rs370127436 | snp | C/T | 0.000153988 | 0.00877328 | missense | WHSC1 | GRCh38.p7 | 4:1978854 | CAGAGCCAGGGAAGC[C/T]GAAGGGGAAGAGGCG | 7468 |
rs370135802 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872001 | GCCTTTGTGCGGCGC[C/T]CCCGGTCCGGGGCGG | 7468 |
rs370152008 | snp | A/G | 1.65436e-05 | 0.00287602 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975031 | GGGGACCCTGCATGG[A/G]GCTCCTGGCTATGGG | 7468 |
rs370152509 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927537 | AGCCTGGCCCACATG[G/T]TGAAACCCCCATCTC | 7468 |
rs370157885 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882422 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 7468 |
rs370179695 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961418 | CCAGCAGCCTTAGTA[C/T]AGGGCAGGGAAGTAG | 7468 |
rs370198793 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884662 | CTCCCAAAGTGCTAG[A/G]ATTATAGGCGTGAGC | 7468 |
rs370203522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976739 | CAGGCTCCTGATGGC[A/G]GCTGCTGCCGCTCTT | 7468 |
rs370211332 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934358 | CAAAGTATTGGGATT[-/T]ACAGGCATGAGCCAC | 7468 |
rs370248106 | in-del | -/TGT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966259 | GTCACTACAAGTTGT[-/TGT]ATGAAGAAGAAAGAT | 7468 |
rs370291132 | in-del | -/GA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970039 | AACCTGGGAAAGAGA[-/GA]AAGAAGGAATGTAGG | 7468 |
rs370294691 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901287 | AAGGGGTCATGTGAC[C/T]TTGAGCAGTGAGCAT | 7468 |
rs370308187 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903279 | GGTTGGGGCCATGCT[G/T]GCTGTGCTTATTTCC | 7468 |
rs370310059 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965466 | AACTTTGAAAAAATA[A/G]TGGCTGAAAAATTCC | 7468 |
rs370332334 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945876 | GTTATGACTTTGGCA[A/C]CTTGCTTCATTTCTT | 7468 |
rs370361450 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913905 | CCTGTAGGGCTGATC[C/T]CTACAGTTCTATGCT | 7468 |
rs370452308 | in-del | -/CTGAGGCAGGAGG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963909 | GGCTGAGGCAGGAGG[-/CTGAGGCAGGAGG]ACTGCTTGAGCCCAG | 7468 |
rs370539090 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919805 | GCTGGGCATGGTGAC[A/G]CGTGCTTGTAATCCC | 7468 |
rs370539325 | in-del | -/TCTTTTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886218 | CCTTTTTTTCTTTTT[-/TCTTTTT]GAGACAGGATCTCAC | 7468 |
rs370570904 | snp | A/G | 7.28637e-05 | 0.00603544 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930587 | CCCAATGAGTTTTAC[A/G]GATTTAACTTCTCAT | 7468 |
rs370605426 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897884 | CACCTGACTCAGCCT[C/T]CTAAAGTGCTGGGAT | 7468 |
rs370637597 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966596 | CGGGAGGCGGAACTT[A/G]CAGTGAGCCAAGATC | 7468 |
rs370661246 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926590 | ATCCTCCCCCCTCAG[C/T]CTTCCTAGTAGCTGG | 7468 |
rs370668893 | snp | C/G/T | 3.86655e-05 | 0.00439676 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918659 | CATGCTAGCAAGTTT[C/G/T]AGAATTTGAGGAACA | 7468 |
rs370675289 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894715 | AGAAGTTGTCTTTCC[C/T]TCATCCTCCCAAGCC | 7468 |
rs370676117 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943779 | AAGATGGTATAAAAA[-/T]GGCTCTGGTTCAATA | 7468 |
rs370713472 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953377 | GATGTTAAGCGCTGT[A/G]TGGTAACTCAGTGTG | 7468 |
rs370714916 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940539 | AGTTTTGGTTTCCTG[A/C]TTTTTAGGGATTACC | 7468 |
rs370760809 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971781 | AAGGAGGGCTTAACA[A/G]CCCTATCAGGTAAAG | 7468 |
rs370770012 | snp | A/C/G/T | 3.31473e-05 | 0.00407096 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975056 | TATGGGGGCAGAGTG[A/C/G/T]CCATCGCTGAGGGCT | 7468 |
rs370778164 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913628 | CCTCGGCTACCAAAC[A/C]GGGAAGGGCCCCCTG | 7468 |
rs370783279 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911628 | AAAAAAAGAAAGAAA[A/G]AAATTGCATAGGAAG | 7468 |
rs370791120 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939555 | AGGAATTCAGAAGAT[A/T]CATCTTTAGAACTTC | 7468 |
rs370804554 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978105 | GCTCTCCAGCCTGGG[C/T]GACAGAGCTAGACTC | 7468 |
rs370847922 | snp | A/G | 1.64814e-05 | 0.00287061 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942403 | TGTACTGCACTTAGA[A/G]TGATGTAATATTCCA | 7468 |
rs370866408 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928652 | CTGCAGGGCGCTTGT[A/G]ACTCTGCTTTGACGA | 7468 |
rs370924486 | snp | A/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926798 | TTTAAAGGCTTTTCT[A/G/T]CCTTTCCTGATCCTA | 7468 |
rs370925712 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895955 | GTGACCACAGACACT[C/G]ACCTGGTGATGAGGA | 7468 |
rs370934527 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920565 | AATTAAGTAAACACC[C/T]TGTATTTATGGGGTA | 7468 |
rs370953747 | in-del | -/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952819 | CAGCCGTGGCCCTTC[-/C]TGCCTACTCACCGGG | 7468 |
rs370989032 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903949 | TTGTGTTAGCCAGGA[C/T]GGTCTTGATCTCCTG | 7468 |
rs371036686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957182 | CCTCCTTCTTGGGAC[A/G]GATTGTAGGGGTGTG | 7468 |
rs371056465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957539 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 7468 |
rs371065571 | snp | C/T | 3.49418e-05 | 0.00417968 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978620 | TTCTGTGTGCTCACA[C/T]CTTGTGTTCTGTTGC | 7468 |
rs371069166 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914083 | GCTAGAGTTCAGTGG[C/T]GGGATCTCAGCTTGC | 7468 |
rs371100224 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961006 | GGTCAGCACGCTTTT[C/T]GTCATGGCCACATGC | 7468 |
rs371130079 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890562 | CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 7468 |
rs371132899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949680 | GAGGCAGGAGAATCA[C/T]TTGAACCCAGGAGGC | 7468 |
rs371134906 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926678 | GTTTCACCATATTGG[C/T]TAGGCTGGTCTCAAA | 7468 |
rs371139429 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923219 | CTAGGCCAGGCATGG[G/T]GACTCACGCCTGTAA | 7468 |
rs371148572 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943765 | AGATGGGGAAAAAAA[-/A]GATGGTATAAAAATG | 7468 |
rs371177497 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955014 | TGAAGCACCTTTGCT[C/T]TGAAAGCTTTTTTTA | 7468 |
rs371191973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949225 | AAGAACAGGATGTGC[C/G]CTGTGGCTCTTGCAG | 7468 |
rs371208366 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948483 | CTTTGCTCTCCTTGC[G/T]GGTGGTTGCCGAGCC | 7468 |
rs371219948 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877085 | GAGGTTGAAATGAGC[C/T]GAGATCATGCTACTG | 7468 |
rs371238694 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889144 | CTCAGGTGATCCACC[C/T]GCTTTGGCCTCCCAA | 7468 |
rs371245410 | multinucleotide-polymorphism | GG/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881869 | GCAGAGAGCAGAACG[GG/TT]GATTGGGTGTTGGCT | 7468 |
rs371273908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937348 | TGTGAGCCACTGCGG[C/T]TGGCCAGGTTACCTT | 7468 |
rs371286749 | snp | G/T | 1.7828e-05 | 0.00298558 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953556 | GCAGCCTTGCTGTGG[G/T]TTCAGATGCAGGCCA | 7468 |
rs371300894 | in-del | -/CA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882713 | GGTTGAGCCAAGTAA[-/CA]GTTTTGGGCTTGTTA | 7468 |
rs371341605 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882488 | CTAACACGGTGAAAC[A/C]CCGTCTCTACTAAAA | 7468 |
rs371416902 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914643 | GAGTATGCTACTTTT[C/G]TATCTTCACACTTGA | 7468 |
rs371464236 | snp | C/T | 6.59435e-05 | 0.00574172 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900936 | AGAACCCGGCGCACA[C/T]GATGCCAAACTGCGT | 7468 |
rs371486720 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882556 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 7468 |
rs371488225 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901972 | TCACGTGGCACTCGG[G/T]ATGGCCCTGACACTC | 7468 |
rs371529672 | snp | A/G | 8.42538e-05 | 0.00648998 | missense | WHSC1 | GRCh38.p7 | 4:1918153 | CAGCTATTGAAACCA[A/G]TTTCAGGGAAATTGA | 7468 |
rs371574308 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935235 | ACCCAGGAAAAGACT[C/G]AGGACGGACAAGCAC | 7468 |
rs371576678 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875673 | TTTGGGAGGCCGAGG[C/T]GGTTGGATCACGAGG | 7468 |
rs371586651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874301 | AATACGTGGTACCAT[A/G]TCCTGACTCCAGGCC | 7468 |
rs371592249 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937507 | GTAATGTTTTATTAG[C/T]TCCTATCTCAGGAGA | 7468 |
rs371607115 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968892 | GAGAATGTGATTCAC[A/G]GCCAAACAAATCTAT | 7468 |
rs371607137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878055 | AATTTAAAAAAAGTA[A/T]TATATATATACACAC | 7468 |
rs371610028 | snp | A/C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978563 | CCTGACAGTTGTAAG[A/C/T]CATCTTCAACCACGA | 7468 |
rs371640889 | in-del | -/AGGAACTGG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956718 | CACTGGAGGAACTGG[-/AGGAACTGG]TATTTATGATCGGTC | 7468 |
rs371647047 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963980 | TCCAGCCTGGGGGAC[A/G]GAATGGGAACCCGGT | 7468 |
rs371657472 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972257 | CGGCAGTGTCACTGA[C/T]GGACACAAGAGATGA | 7468 |
rs371671528 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968476 | TGTTAAAGTATACAT[A/G]TGACGTCTACATGGG | 7468 |
rs371674866 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930835 | TGTAGCAAGCTGAGC[C/T]CTGATCTTGGAACCG | 7468 |
rs371675831 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955356 | GTGAGGGGCCTGGGG[A/G]TGTCTGCGGCACACG | 7468 |
rs371687912 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924302 | TGACAGCTAGGCCTG[C/T]GCAGGGTTGGTGAGG | 7468 |
rs371688349 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922834 | GGGAGGCTGAGGCTG[C/G]AGAATTGCTTGAACC | 7468 |
rs371694770 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913611 | CCCCTCTCTCTCTCT[-/CT]GCCTCGGCTACCAAA | 7468 |
rs371707404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944597 | AACTTGTCAGAATAT[A/G]TAAAAGCTTAGATTG | 7468 |
rs371724422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884594 | AGATGGGGTTTCACT[A/G]TGTTGGCCAGGATGG | 7468 |
rs371750049 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934322 | ACTCCCGACCTCAGG[C/T]GATCCGCCCACCTCA | 7468 |
rs371818221 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965475 | AAAATAATGGCTGAA[A/G]AATTCCCAGGTTTGA | 7468 |
rs371879505 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921775 | CAACACAGCAAGACT[-/CT]GTCTCAAAAAAAAAA | 7468 |
rs371886313 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946392 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 7468 |
rs371893111 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885774 | TGCACCGGTTCTGCA[A/G]AGCTGCCCTGAGTAC | 7468 |
rs371927532 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975669 | TGGGCAGGGCCGTGC[A/G]CCCTCTGAAGGTTCC | 7468 |
rs371954667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887831 | TATCTGTTACTAATT[C/G]AGCCTAAAGTTTTTC | 7468 |
rs371964723 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892847 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 7468 |
rs372056394 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981373 | TGGGTGTGGCTGGCT[C/G]TCGGCCCTGCCCAGC | 7468 |
rs372061429 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960028 | ACCATGCCCTAATAA[G/T]TTTATTTTTTTTTGG | 7468 |
rs372062813 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943708 | CATGAAAAAGCTCAA[G/T]AGTAAAATTAAAATT | 7468 |
rs372070040 | snp | A/C/G | 0.0142815 | 0.0833581 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903731 | TGAGAGTGAGAGAGA[A/C/G]ATTTTTTTTTTTTTT | 7468 |
rs372090405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929404 | GAGTGTTACTGCCCC[C/T]GTTTCACAGAGTGGA | 7468 |
rs372125946 | in-del | -/T | 0.99674 | 0.0132492 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938402 | CCTTTTTTTCTTTTC[-/T]TTTTTTTTTCTTTCT | 7468 |
rs372147092 | snp | C/G | 1.72193e-05 | 0.00293417 | missense | WHSC1 | GRCh38.p7 | 4:1900688 | CAGAGTCCCCTTTCT[C/G]TTCAGAGTGTTGTAA | 7468 |
rs372152580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908399 | ATTGTGGGATGTAGA[A/G]TAGGAGGCACAAGCA | 7468 |
rs372274419 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959995 | CTTCCCAAGCAGCTG[A/C/G]GACTACAGGCGTGTT | 7468 |
rs372278519 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898210 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCAGGGACT | 7468 |
rs372282432 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928986 | ATGCAGGGCTGGGGA[C/G]AGGGACCCCACAGGG | 7468 |
rs372296910 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974517 | CTGCGCCCAGCCAGG[G/T]TGAGTCTTGTTCTTG | 7468 |
rs372303057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917538 | CCCCTCCGGGTTCAA[A/G]CGATTCTCCTGCCTC | 7468 |
rs372451342 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892144 | CTTTATTTTTATTTC[C/T]TTATTTTTATTTTAA | 7468 |
rs372468764 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939279 | GTTACTTTTAAGTGT[A/G]GGAGTAGCATTGTGG | 7468 |
rs372469871 | in-del | -/TTATT | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880938 | TTTATTATTGAGGAA[-/TTATT]TTTATTTTTAGCTGT | 7468 |
rs372484492 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897175 | ACTCTGTCTCAAAGG[A/G]AAAAAAAAAAAGGAA | 7468 |
rs372548092 | snp | C/T | 1.67321e-05 | 0.00289236 | missense | WHSC1 | GRCh38.p7 | 4:1930641 | GTGGTAGCTGAGCAC[C/T]CAGATGCTTCAGGTG | 7468 |
rs372572706 | snp | A/G | 0.00017256 | 0.00928711 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955673 | AGGCTAAGCCTGGCC[A/G]CCTCGCCCTCCTCTT | 7468 |
rs372588729 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888219 | GGAGTTCGAGACCAG[C/G]CTGGCCAACATGGTG | 7468 |
rs372595953 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911620 | AAAGAAAAAAAAAAA[A/G]AAAGAAAGAAATTGC | 7468 |
rs372604083 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883540 | AGGAGGCTGAGGCAC[A/G/T]AGAATTGCTTGAACC | 7468 |
rs372636114 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909650 | ATCCTTTTTTTTTTT[C/T]TTTTCCTGGAGATGG | 7468 |
rs372660600 | in-del | -/AA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911587 | GCGAGACGCCATCTC[-/AA]AAAAAAAAAAAAAAA | 7468 |
rs372709450 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961505 | ATTTTATTTTTTAAT[C/T]TTCAGTGCTCTTTGG | 7468 |
rs372739936 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917778 | AAATGTAAAAGTATT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs372740479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929773 | CCTGTGCCCTGCTCT[C/T]GAGATCCGTGGCTCT | 7468 |
rs372789667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899259 | GCGGGTTGCAGACAC[A/C]AGCAGCCCCCTATTG | 7468 |
rs372794372 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960541 | TGACCCAGGTCCATA[A/C]CAGGGCTGACCCAGC | 7468 |
rs372805518 | snp | A/G | 3.29674e-05 | 0.00405988 | missense | WHSC1 | GRCh38.p7 | 4:1916918 | CAGTTCTTTGGTGAC[A/G]CCCCAGAAAGAGCTT | 7468 |
rs372843608 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926413 | CTGCCTCAGCCTCCC[A/T]AAGTGCTGCGATTAC | 7468 |
rs372845209 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967458 | TGGCGGGCGCCCATA[A/C]TCCCAGCTACTCAGT | 7468 |
rs372860761 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979801 | TTCACAAATCACCAC[C/T]GACTGAAGTGTGTGT | 7468 |
rs372897022 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934612 | CCCAGCACTTTGGGA[A/G]GCCGAGGCAGGCGGA | 7468 |
rs372898352 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874416 | TGTGACCTTTCTCCC[C/T]TGTTGGGTTAACTCT | 7468 |
rs372939339 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899729 | TTTGCAGGGAAGACC[C/T]CACACCAGCATGCTG | 7468 |
rs372990511 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913187 | GTGAGCCCTCTGTCA[C/T]GCCCAGACAGGGCCA | 7468 |
rs372993257 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980940 | GGCCGGGCAGTGTCC[C/T]CACACACACCTTAGA | 7468 |
rs372999293 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963282 | CAGGAGCTTGTGTTT[A/T]AACCCTCATGTGGGG | 7468 |
rs373003169 | snp | C/T | 0.000137057 | 0.00827705 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955754 | TGACTGCCTGAACAT[C/T]GAGATGCCTGACGGC | 7468 |
rs373006516 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901960 | GTCTCCACGCCTTCA[C/T]GTGGCACTCGGGATG | 7468 |
rs373024601 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930948 | AGCTTCTGCCATCTG[C/T]GTTTACTGGCTTATG | 7468 |
rs373078642 | snp | C/G | 3.31791e-05 | 0.00407289 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959762 | GTCGTTATCCCCTCC[C/G]CTGCTTTTGAGAAAT | 7468 |
rs373093849 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872635 | GAGAGAGAGAGAGAG[A/C]GCGCGCAGACCCTGT | 7468 |
rs373114576 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878287 | TTTTTTTTTTTTTGT[A/T]TTTTTAGTAGAGACT | 7468 |
rs373161300 | snp | C/T | 3.30464e-05 | 0.00406474 | missense | WHSC1 | GRCh38.p7 | 4:1901148 | AACCAGAAAACAAGG[C/T]GAGAAGGAACAGGAA | 7468 |
rs373166571 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924303 | GACAGCTAGGCCTGC[G/T]CAGGGTTGGTGAGGT | 7468 |
rs373223010 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918995 | TCTACAAAAATTAGC[C/T]GGGTGTGGTGGCACA | 7468 |
rs373246455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906254 | TTTTAATTTCTTTTT[C/T]TGGGGATGGAGGCTC | 7468 |
rs373255342 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974958 | CAAGTGGACAGTGAA[C/T]GGGGACACTCGTGTG | 7468 |
rs373257735 | snp | A/G | 8.27137e-05 | 0.0064304 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938540 | CCAGGCAGGTAATGT[A/G]GTCAGCGCCCTTTCC | 7468 |
rs373272646 | snp | A/C | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1948900 | TTAAGTTTGTTCCAC[A/C]ACGTTAAGGGAAGAG | 7468 |
rs373286964 | snp | A/G | 0.000153988 | 0.00877328 | missense | WHSC1 | GRCh38.p7 | 4:1901085 | TTGAATCTTCCATTT[A/G]TGGTGACAGTGCTGC | 7468 |
rs373317595 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894201 | ACCTCGAGTGATCTT[C/G]CCACTTCAGCCTCCC | 7468 |
rs373336185 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895742 | GTTCTCAGGTTTCCC[C/T]GCAGGTCCTACCAGT | 7468 |
rs373349026 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947510 | AGTTTGTGTAACCTA[A/G]AAGGGTCACTTTAAT | 7468 |
rs373368163 | snp | G/T | 5.22243e-05 | 0.00510974 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959452 | GTGTGGACCAAGACA[G/T]CTTACTCCTTCCCTG | 7468 |
rs373375888 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977235 | GGAAAGTAGAGTGGG[C/T]TCCACCTTCCAGCAC | 7468 |
rs373377272 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932331 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 7468 |
rs373395528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964650 | GCCGTTGTTATCACA[C/T]CTCCCTCAGTCGTTA | 7468 |
rs373414282 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890690 | CACTGCAACCTCCGC[C/T]TCCTGGGTTCCAGTG | 7468 |
rs373414884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910484 | AGAAGATAACTATAT[A/G]TTTTAGATATTACAC | 7468 |
rs373449037 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945231 | GGAACAAGACGGGGT[C/G]GGGTGGGGAGATGGG | 7468 |
rs373450281 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948540 | GGCTAGTTGTCTGTC[C/T]GGTGGCTGGGAGGGG | 7468 |
rs373488490 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970680 | AGGAGCAAAGGAGAG[C/T]ATGAAGATAATGCTA | 7468 |
rs373501773 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922268 | ATAGAGTTCACCAGG[A/T]TATAAAATTAACATA | 7468 |
rs373502806 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895520 | CTATATTCAACTCAA[C/T]TGAGTTTTTAATTTC | 7468 |
rs373512421 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894709 | AAAAGAAGAAGTTGT[C/G]TTTCCCTCATCCTCC | 7468 |
rs373556731 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896692 | CCTCCCTTCCTTCCC[C/G]AACTCTTCCATTCCT | 7468 |
rs373627642 | snp | C/T | 0.000128512 | 0.00801496 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901266 | GGTATTTAGGAGACG[C/T]TGTGTAAGGGGTCAT | 7468 |
rs373665168 | snp | A/G | 4.96413e-05 | 0.00498179 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955869 | GAGACATAGAATCGT[A/G]TGCTTTTATGTCTTT | 7468 |
rs373696085 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879825 | TGGGCCCATGGCACT[-/TG]TGTGTGTGTGTGTGT | 7468 |
rs373748031 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955300 | GGGGAAGCGACACCA[C/T]GCCCACGTCAACGTG | 7468 |
rs373754992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978349 | CCTGCCTGTCCACGC[C/T]GCGCTGGGGGACACT | 7468 |
rs373762613 | snp | A/G | 0.00125431 | 0.0250116 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978918 | CAAATAGCGCCAGGC[A/G]GCCGCTTGGCCGGAT | 7468 |
rs373768444 | snp | C/G | 3.48371e-05 | 0.00417341 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974721 | GTTTGGGGGTGTCCT[C/G]TCTCAGTGGACACAG | 7468 |
rs373772824 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899090 | TTTTAAGAAATTGTG[C/T]GGGTCAGACAGAACA | 7468 |
rs373789286 | snp | A/G | 8.27438e-05 | 0.00643157 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976480 | TTGACTCTAGACCTC[A/G]ACGACCCTTTCATCA | 7468 |
rs373798315 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896779 | TTCTTCTCTTTTTTT[-/T]CTTTTCTTTTCTTTC | 7468 |
rs373799057 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898392 | TTTCGTGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 7468 |
rs373808726 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918638 | GGTCAGTACTAAGTT[A/G]TGTTTCATGCTAGCA | 7468 |
rs373846473 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978214 | TGTTGGCCATGGGTG[C/T]GAGAGGGTGGTCCCT | 7468 |
rs373858386 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883067 | TCTGGAGTAAAATTG[A/G]TAAGTTGTGTTGTTT | 7468 |
rs373866725 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902849 | AATAAATGTAAACCT[C/G]GGTTGCTGTGCAGTA | 7468 |
rs373867838 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915365 | GTGGTCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 7468 |
rs373874155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958376 | GGAGTCAGTCACATA[C/T]GGCCAGGGCTCAGTG | 7468 |
rs373876517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888846 | ACTGGGATTACAGGC[A/G]TGAGCCACCACGCCT | 7468 |
rs373888225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947039 | GGGGGTCCTGGTCCG[G/T]CTGATGGGGGTTTGC | 7468 |
rs373904948 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955380 | GCACACGCCTCTCAC[A/C]CTCCCAGGAGCCACA | 7468 |
rs373944823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907872 | CACCTTGGCCTCCCA[A/G]TGGGATTACAGGCAT | 7468 |
rs373976765 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938870 | TGGTGCCAGTTGCTA[C/G]TGTAAATTCTGTCAC | 7468 |
rs373990613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877741 | AGCTCTGCTGCCTCC[A/G]ACTAGTGCCCTTGTT | 7468 |
rs374002065 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879194 | ATGTAAATATATACA[A/G]CACTTTTTAAAATTA | 7468 |
rs374024971 | snp | C/T | 1.71693e-05 | 0.00292991 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953519 | CAAACCCAAGGCCGT[C/T]AAAAGGTACAGGTGC | 7468 |
rs374034896 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965768 | TACCTTTGCACATGG[C/T]GGCAGGAGAGAGAAG | 7468 |
rs374037313 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903653 | CAAGGAAATAGATTT[A/G]TATAGAGATCTTCAA | 7468 |
rs374038888 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979201 | CAAGGTTCCCTCCCA[C/T]TCTATTTTTTTAGGT | 7468 |
rs374078635 | snp | C/T | 5.0606e-05 | 0.00502995 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960999 | GAGGATTGGTCAGCA[C/T]GCTTTTTGTCATGGC | 7468 |
rs374135543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964081 | TCGTGAGCAGACCTT[C/T]CTAATGGAAGGCTTT | 7468 |
rs374150342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889587 | GCTTACTGTAACCTC[C/T]GCCTCCTGAGTTCAA | 7468 |
rs374363774 | multinucleotide-polymorphism | AA/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932594 | TCTACTAAAAATACA[AA/CT]ATTAGCCAGGCGTGG | 7468 |
rs374391148 | in-del | -/T | 0.0626037 | 0.165477 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934075 | TTAGTAAGGAAAAGA[-/T]TTTTTTTTTTGTTTT | 7468 |
rs374417585 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918875 | AGAACAGGCCAGGCA[C/T]AGTGGCTCATGCCTG | 7468 |
rs374426276 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886717 | GTGGCGTGCACCTGT[A/G]GTCCCAGCTACTCAG | 7468 |
rs374461444 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895018 | TGGGGACCTCATGTA[C/T]GTGGAATTTTACAGT | 7468 |
rs374487416 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949486 | AGCCCACTCTGGCTG[C/G]GTGCGGTGGCTCATG | 7468 |
rs374491217 | snp | A/G | 1.68946e-05 | 0.00290638 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952078 | AAGGGACTGCCGGGC[A/G]CTGCTTACCCGCCTG | 7468 |
rs374501835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923513 | TCCTGGTGGGATGGT[C/T]CTTCACAGTCATCCT | 7468 |
rs374502404 | snp | C/T | | | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975008 | ACATTCCTGCAGGTA[C/T]AAGCTCTGGGGACCC | 7468 |
rs374513455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928215 | CTTGTTTTTTGATAT[A/G]TTAAGAATAAAGAAG | 7468 |
rs374514589 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935422 | GCATTTCTTACAGAA[C/T]CCCATTGAGAAAGGC | 7468 |
rs374516967 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948482 | ACTTTGCTCTCCTTG[C/T]GGGTGGTTGCCGAGC | 7468 |
rs374520069 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875428 | CTGGGACAACAGGCA[C/T]GTGCCACCATGCCTG | 7468 |
rs374524480 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978568 | CAGTTGTAAGTCATC[A/T]TCAACCACGATAATG | 7468 |
rs374545543 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906656 | TCTCTCTCTCTCTCT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs374571937 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882350 | ACTGTGGAAACAAAC[A/G]GATATGTACTATGGG | 7468 |
rs374584681 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899203 | ATTTGCTCTTTTTTT[-/T]CCTGTCTCCTTCCTC | 7468 |
rs374601007 | snp | C/G | 0.00017468 | 0.00934396 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978621 | TCTGTGTGCTCACAT[C/G]TTGTGTTCTGTTGCA | 7468 |
rs374614167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972598 | GGGCCGGGCAGCCCA[C/T]GTACCACGCACTGAT | 7468 |
rs374618248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932383 | GGCAGAGGTTGCAGT[A/G]AGGCAAGATCACGCC | 7468 |
rs374622289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896488 | ATCCTCACACCTCAG[C/T]CTCCCGGGTAGCTGG | 7468 |
rs374653221 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914098 | CGGGATCTCAGCTTG[C/G]TGCAACCTCTGCCAC | 7468 |
rs374703015 | in-del | -/TCTCTTCCTTCC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896690 | CCCTCCCTTCCTTCC[-/TCTCTTCCTTCC]CGAACTCTTCCATTC | 7468 |
rs374709418 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978705 | TTCATTTTGCCACCT[C/T]TGCCCCAATTCGTTC | 7468 |
rs374710093 | in-del | -/G | 0.00260659 | 0.036007 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948575 | GGTGGGAAAAAGTCG[-/G]AATCTCTGCAATCTG | 7468 |
rs374816850 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891881 | AAAAAACAAAAAAAA[A/C]CAAACAAAAACGAAA | 7468 |
rs374886868 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900047 | TTCATCAACCTGGAG[C/G]TAATCCTGTGCTTGG | 7468 |
rs374892759 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975714 | CCCAGGCCTGTCTCC[C/T]GTTCCTGGTGGCGGC | 7468 |
rs374905284 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965112 | TATGGCCATTTAAAG[A/G]GAAAACAAAATCAGC | 7468 |
rs374919822 | snp | C/T | 6.03276e-05 | 0.00549183 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955363 | GCCTGGGGGTGTCTG[C/T]GGCACACGCCTCTCA | 7468 |
rs374943425 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939795 | TAAAATAATAATAAT[A/G]ACGATAACCATGGCA | 7468 |
rs374965509 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908837 | CAGGCTAGAGTACAG[C/T]GGCACAATCATAGCT | 7468 |
rs375010894 | snp | A/C/T | 8.23681e-05 | 0.00641702 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974858 | TATATCACTTGACCT[A/C/T]ACAGGACCGTATAAT | 7468 |
rs375016434 | snp | A/G | 9.32705e-05 | 0.00682836 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974638 | CCTGTCCTCCCCGGC[A/G]CTCACTAAGGCTCGG | 7468 |
rs375023402 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930844 | CTGAGCTCTGATCTT[G/T]GAACCGTAGGGAAGT | 7468 |
rs375044319 | in-del | -/AC | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882712 | GGGTTGAGCCAAGTA[-/AC]AGTTTTGGGCTTGTT | 7468 |
rs375045284 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939800 | AATAATAATAACGAT[-/A]AACCATGGCATTGGT | 7468 |
rs375052981 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961557 | TGTTGTGTAGCAGAA[C/T]CGTTTTTGCTTGGTT | 7468 |
rs375105245 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880755 | ATAAGACCAGTAAGC[C/T]ATACTCATCAACAGG | 7468 |
rs375129793 | in-del | -/CTC | 0.00676609 | 0.0577691 | utr-variant-3-prime, cds-indel | WHSC1 | GRCh38.p7 | 4:1979248 | ATGGAATGTTTTAAT[-/CTC]CTCTGAAATGTGTAG | 7468 |
rs375161669 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972011 | CCGCTCCTGTACCCC[C/T]AAGGCTGCGGGTGCT | 7468 |
rs375178857 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913786 | CCGCATCTTGGTGGT[A/G]GTGGTGTCCCCTGTG | 7468 |
rs375184325 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972993 | GAGTAACTGGGATTA[C/T]CGGTGCCCACCACCA | 7468 |
rs375193549 | snp | C/T | 8.38061e-05 | 0.00647272 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975413 | AAGGTAAGGCTGTGG[C/T]GCCCTCCTTCCCCCC | 7468 |
rs375197958 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945058 | GACAGGAGTCGGGGG[A/C]TCCTCTGTCCCACTG | 7468 |
rs375200122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885532 | GTGGCCCCTGTTGAC[A/T]TGTATTTTGATAGGA | 7468 |
rs375203006 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880398 | CAGCAGTCTATATGT[A/G]CATGGAAGACTGAGC | 7468 |
rs375203552 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939799 | ATAATAATAATAACG[A/G]TAACCATGGCATTGG | 7468 |
rs375203591 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881205 | ACCTCAGCCTCCTGC[A/G]TAGCTGGGACACAGG | 7468 |
rs375231406 | in-del | -/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938412 | TTTTCTTTTTTTTTT[-/C]TTTCTTTTTTTTTTT | 7468 |
rs375235763 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937674 | CTGTCGCCTTGTCCA[C/T]GATCCTCTGGATTCC | 7468 |
rs375249643 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878436 | TTAATTATTCTGTTG[C/T]TATCTGGCACTCCAC | 7468 |
rs375253637 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910266 | AGTCTTTCTCTGTCA[C/T]CCAGGCTGGAGTGCA | 7468 |
rs375260041 | snp | A/C/G | 4.9675e-05 | 0.00498348 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955894 | GTCTTTTCTGTTCAC[A/C/G]TGTGTTCGCTTTACA | 7468 |
rs375263146 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968585 | TTTAGTAGAACCTGC[A/G]GGAGGAAGATGGGGG | 7468 |
rs375277590 | snp | A/G | 3.2963e-05 | 0.00405961 | missense, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974986 | GTGGGCCTGTTTGCC[A/G]TCTGTGACATTCCTG | 7468 |
rs375362878 | in-del | -/TCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898031 | TTTTTCCCTCCTCCT[-/TCT]GGGTGGAACTCCAGA | 7468 |
rs375384250 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893086 | CCTCTAAGTCCGCAT[A/C]CCCAGGTTTGACATC | 7468 |
rs375434376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967565 | CCCAGGCAACAGAGC[A/G]AGACTTTGTCTCAAA | 7468 |
rs375449205 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907128 | AATGAACTTAATCTC[G/T]CTAAGCTTCAGTTTC | 7468 |
rs375450754 | snp | C/T | 0.00131314 | 0.0255899 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929444 | AGTGCCTTCACTTGC[C/T]GAAGTCCACAGAACT | 7468 |
rs375518598 | in-del | -/TC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917252 | CTCATTTGATGACTC[-/TC]AGAGATAACTTGTTT | 7468 |
rs375522546 | snp | A/T | 0.000307953 | 0.0124049 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930597 | TTTACGGATTTAACT[A/T]CTCATTGCACCTTCT | 7468 |
rs375536140 | snp | C/G | 0.000875616 | 0.0209055 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925039 | CTCCCCTGGACTCTG[C/G]CTGGGTGGTTTTGAA | 7468 |
rs375547934 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879497 | ATGCTGGGATTACAG[A/G]CTTGAGCCACCGCGC | 7468 |
rs375552752 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941632 | ATGTGAAATTAATAC[A/C]CCTTCCTACATTTTG | 7468 |
rs375556718 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921859 | ACGGAAAATAGTAGC[C/T]AATATTAGGCCGGGC | 7468 |
rs375561165 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942468 | CTCAGTGACATTTCT[A/G]TCACAATCATTTTAT | 7468 |
rs375567006 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977252 | CCACCTTCCAGCACC[C/T]GCATTTCAGAGATGA | 7468 |
rs375567930 | in-del | -/GGT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887784 | CTTTGTTTTCCTGGT[-/GGT]AAGTTTTTCTGTTGG | 7468 |
rs375573002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961855 | ACTTCAGCTGGGGAA[A/G]TGTGGCCTCCTTAGT | 7468 |
rs375603487 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886179 | AGAGTTCCATCAAGG[A/C]AACCTCTGCTCTTTC | 7468 |
rs375604703 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938371 | TTTCCTTTTGTTGTT[C/T]TTTTTCTTTTTTTTT | 7468 |
rs375609366 | snp | A/C/G | 0.000165953 | 0.0091078 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952122 | GCTGTGTGAGAAGCC[A/C/G]GGCAGCCTCCTGCTC | 7468 |
rs375620630 | snp | A/G | 4.94368e-05 | 0.00497152 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951101 | GGGAGACGAGCCCTC[A/G]GAGTCCCCATACGAA | 7468 |
rs375640116 | snp | A/C/G | 6.96978e-05 | 0.00590294 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978624 | GTGTGCTCACATCTT[A/C/G]TGTTCTGTTGCAGGG | 7468 |
rs375667402 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932697 | ATTGCAGTGAGCCGA[A/G]ATCGTGCCATTGGAT | 7468 |
rs375706303 | in-del | -/TA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872956 | AGAACGCCAACAACA[-/TA]AAGCAAACAAGTTCT | 7468 |
rs375757398 | snp | A/G | 0.000348765 | 0.0132008 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955936 | ATTGAAATTATTATC[A/G]CTGTCTCTGAGGAGT | 7468 |
rs375760751 | snp | C/T | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982679 | GAGGGACTGGGTCCC[C/T]GGAGCAGGGAGGACA | 7468 |
rs375772720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892634 | GTAGTGGCCTGATCT[C/T]GGCTCGGCTCATTGT | 7468 |
rs375807158 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878915 | AGCGTGAGAGTGGTG[C/G]AGGAGAGGGTCCTTG | 7468 |
rs375859980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917995 | CATGTTGACCAGGCT[A/G]GTCTTAAACTCCTGG | 7468 |
rs375867118 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874100 | AATCAGCAGCAACAG[A/G]AGCCATAAGGCTTTT | 7468 |
rs375868358 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976199 | CCATCAGCAGATCCT[A/G]GAGCTGTGTGTCTGC | 7468 |
rs375877771 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933657 | CCTCGGCCTCCCAGA[C/G]TGCTGGGATTACAGG | 7468 |
rs375879807 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904508 | CTTTACCTAAAGTTA[A/G]TGATTGATTCAAGTG | 7468 |
rs375912929 | snp | A/G | 1.68103e-05 | 0.00289911 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961172 | GCGGAACTCCACTGT[A/G]AGCTTCTGCAGTGTG | 7468 |
rs375934281 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954174 | ATTTTTAGTAGAGAC[A/G]GGGTTTCATCATGTT | 7468 |
rs375961181 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929835 | AAACCTTTAACTCAC[G/T]GAGGCCAGACCCGGT | 7468 |
rs375995389 | snp | A/G | 3.31818e-05 | 0.00407306 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918230 | CATGTCAGTGGAGGA[A/G]CGGAAAGCCAAGTTC | 7468 |
rs375999450 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898480 | CCATCCTGGGTAACA[C/T]GGTGAAACCCCGTCT | 7468 |
rs376020209 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891718 | AAAAATTAGCCGGGC[A/G]TGGTGGTCGGCACCT | 7468 |
rs376041814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919715 | GAGGCGGGTGGATCA[C/T]GAGGTCAGGAATTTG | 7468 |
rs376067363 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911624 | AAAAAAAAAAAGAAA[A/G]AAAGAAATTGCATAG | 7468 |
rs376073914 | snp | A/G | 1.68199e-05 | 0.00289994 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961007 | GTCAGCACGCTTTTT[A/G]TCATGGCCACATGCT | 7468 |
rs376083183 | snp | A/G | 1.65416e-05 | 0.00287586 | missense | WHSC1 | GRCh38.p7 | 4:1935161 | AATGTAAATGGGAAA[A/G]AAAGAAACCACACAA | 7468 |
rs376148523 | snp | G/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893747 | ACAAGATTTCGCCAT[G/T]TTGCCCAGGCTGGTC | 7468 |
rs376187371 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977723 | GGAGGTTGCAGTGAG[C/T]CAAGATTGCAGAAAG | 7468 |
rs376221213 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964398 | GAAGGCTTGCAACTT[A/C]CAGGGGAGGCTTGGA | 7468 |
rs376225140 | snp | A/T | 0.0013233 | 0.0256885 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942306 | TCCTTTAGTAGAGCA[A/T]ATTCTTATTTTTTTC | 7468 |
rs376253701 | snp | C/T | 6.62965e-05 | 0.00575707 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958062 | GGAGCTGCGTGCACG[C/T]GTGTGGAGGGAGTCT | 7468 |
rs376259565 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875845 | ACCCAGGAGGCGGAG[C/G]TTGCAGTGAGCCAAG | 7468 |
rs376266710 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903160 | GGCAAGGTTTTGGGC[C/T]GGCCTCTTCAGCTTA | 7468 |
rs376267055 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964911 | CATCTTGGGTTGATC[C/G]TCTGCACAGAAACAG | 7468 |
rs376329213 | snp | A/T | 3.64578e-05 | 0.00426937 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901255 | TCAGATAAAAAGGTA[A/T]TTAGGAGACGTTGTG | 7468 |
rs376347577 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927392 | CTAAACATTCTTCGC[C/T]GAATCCTGAAAGCAA | 7468 |
rs376358486 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943064 | ACTGTAATCAGGTTA[G/T]GTACACCAACCTCTG | 7468 |
rs376440192 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902093 | GGTGGTCTATAGGGT[A/G]TTGCTTTTTAGTTGT | 7468 |
rs376461775 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917054 | TGATAGATGACCCTT[C/T]AGTCTACTTTTAGAC | 7468 |
rs376511575 | snp | C/T | | | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1871453 | CCGCCGCCGCCCCCT[C/T]CCCGCCTGGGCCCTA | 7468 |
rs376542410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890818 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 7468 |
rs376544920 | snp | A/C/G | 6.59482e-05 | 0.00574198 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959575 | TTGTGGCTTTGATTC[A/C/G]GAGTGTCTGAACAGG | 7468 |
rs376545978 | snp | A/G | 1.67374e-05 | 0.00289282 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918494 | TCCTCAAAAGACGGC[A/G]GAGGCTGACCCCAGA | 7468 |
rs376547016 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911623 | GAAAAAAAAAAAGAA[A/G]GAAAGAAATTGCATA | 7468 |
rs376558692 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981086 | GCAGATATTAACTTA[C/T]TTTTGTGTTGGACAG | 7468 |
rs376575716 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979695 | CTAGGTTCTTATCAA[C/T]ATTTGGGGGATAACT | 7468 |
rs376585881 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924312 | GCCTGCGCAGGGTTG[C/G]TGAGGTGCTGTATGC | 7468 |
rs376604115 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965702 | ATGACTCACAGTTCC[A/G]CATAACAGGGGAGGC | 7468 |
rs376608408 | in-del | -/GCCTGCCGTCAGCGTGGC | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951773 | TGCCGTCAGCGTGGC[-/GCCTGCCGTCAGCGTGGC]ACCTGCCATCTGGAT | 7468 |
rs376629334 | snp | C/T | 6.25332e-05 | 0.00559131 | missense | WHSC1 | GRCh38.p7 | 4:1976583 | GAGGACGAGTGCTTC[C/T]GCTGCGGTGATGGCG | 7468 |
rs376631585 | snp | C/T | 8.41379e-05 | 0.00648551 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976585 | GGACGAGTGCTTCCG[C/T]TGCGGTGATGGCGGG | 7468 |
rs376638264 | snp | A/G | 0.000153988 | 0.00877328 | missense | WHSC1 | GRCh38.p7 | 4:1900944 | GCGCACACGATGCCA[A/G]ACTGCGTTTTGAGTC | 7468 |
rs376652101 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977650 | GTGTGGTGGCATGCA[C/G]CTGTAATCCCAGCTA | 7468 |
rs376670595 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947113 | GTCATTGTCCTCAAG[C/T]CCTTCGCAGACAGTG | 7468 |
rs376700701 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907546 | AGTCAAAGTAAAACA[-/G]CACAGCAGACACCTA | 7468 |
rs376706695 | snp | C/T | 5.28239e-05 | 0.00513898 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953540 | GTACAGGTGCACCTG[C/T]GCAGCCTTGCTGTGG | 7468 |
rs376738534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922432 | GCAGACCTCAATAAA[G/T]ATGTATTTATATATA | 7468 |
rs376750304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885781 | GTTCTGCAGAGCTGC[A/C]CTGAGTACAGGTAGT | 7468 |
rs376796720 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956856 | TGTGTGACTGCAGGC[A/G]GGGACCCGCGTATTT | 7468 |
rs376801513 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909743 | TTTCCCAGGTTCAAG[C/T]GATTCTCCTGTCTCA | 7468 |
rs376808083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937346 | GGTGTGAGCCACTGC[A/G]GCTGGCCAGGTTACC | 7468 |
rs376840497 | snp | C/T | 1.67466e-05 | 0.00289362 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952257 | ACGGGCGGGCAGCTC[C/T]GCAGCCTGGCCGGCC | 7468 |
rs376862120 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955887 | CTTTTATGTCTTTTC[C/T]GTTCACATGTGTTCG | 7468 |
rs376887290 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938949 | TATTTATATTTCACA[G/T]GCTAAAGAAACTAGC | 7468 |
rs376936974 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975273 | TGTTTCCAATTTGGT[A/G]TCTGTCTCCTCTTCT | 7468 |
rs376941345 | snp | C/T | 0.000697757 | 0.0186653 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974771 | CAACAAGGAACACAA[C/T]TTGTTCAATGTGCTT | 7468 |
rs377028651 | snp | A/G | 0.000157988 | 0.00888644 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918109 | TTATGTTTGTGTAGT[A/G]AAACTTACAGTGTCT | 7468 |
rs377029248 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913527 | TTCTAGATAGCAATA[A/G]CAGAATTGGTGAGAA | 7468 |
rs377084376 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958255 | GTGTGAGGCTTGGCT[-/T]GGTAGCTTAGAGAAG | 7468 |
rs377101630 | snp | C/T | 7.31422e-05 | 0.00604696 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930586 | ACCCAATGAGTTTTA[C/T]GGATTTAACTTCTCA | 7468 |
rs377159304 | snp | A/C/T | 4.97346e-05 | 0.00498651 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951060 | ACTGTCATCCGCCTC[A/C/T]TTCATCTCTAGGTCT | 7468 |
rs377175663 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925389 | ATTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs377181472 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980126 | GCCTGGCAGGTGTGC[A/G]TGCCTCGTACGTGTG | 7468 |
rs377195739 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953827 | AGAGATAGAGTCTTG[C/G]TCTGTTACCCAGGCT | 7468 |
rs377197653 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893550 | TGTTTTTTGTTTTTT[G/T]TTTTTTTTTGTTTTG | 7468 |
rs377199754 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924509 | CTTTTTGGGACCCAA[A/G]TTGATCTCAGATGGT | 7468 |
rs377220771 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920549 | ATTCATTGCTTTTTT[A/T]AATTAAGTAAACACC | 7468 |
rs377249050 | snp | G/T | 1.68843e-05 | 0.00290549 | missense | WHSC1 | GRCh38.p7 | 4:1955771 | AGATGCCTGACGGCA[G/T]CTGGTTCTGCAATGA | 7468 |
rs377254495 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960956 | CCGTTCTAAGTGATC[A/C]TGATGGGGAGTCTTG | 7468 |
rs377256562 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898305 | TTGCCCAAGCTGGTC[C/G/T]TGAATTCCTGGACTT | 7468 |
rs377256701 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929347 | AGGTGGTAATGGTAA[A/C]CAACCAACATTAACC | 7468 |
rs377268240 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937529 | CTCAGGAGATAGCAC[A/G]TGATAAAAAGAAGTA | 7468 |
rs377280139 | snp | A/G | 1.66546e-05 | 0.00288566 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956109 | CTGGACGCATCAGGC[A/G]CGAGTGTTCCCGTAC | 7468 |
rs377282154 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | WHSC1 | GRCh38.p7 | 4:1916939 | GAAAGAGCTTGGATA[C/T]TTGAGAAGAGCCTCG | 7468 |
rs377290033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948497 | CGGGTGGTTGCCGAG[C/T]CGAGAGCATTGGATC | 7468 |
rs377303444 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908868 | CACTCCAGGCTCAAA[C/G]TCCTGGGCTCAGGTC | 7468 |
rs377306375 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936350 | TTTAATTAGACTTTG[G/T]ACTTTGTTTGAATTT | 7468 |
rs377320517 | snp | A/C | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949111 | CTCCAGTCTCATCTC[A/C]GAAGTGCTCAGGTCT | 7468 |
rs377389068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913460 | ATGCTGTGCTTCAGC[A/G]GTCACGCTCCTGGTC | 7468 |
rs377393200 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926509 | AGGGTCTCACTCTGT[C/T]GCCCAGGCTGGATTG | 7468 |
rs377393719 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880768 | GCCATACTCATCAAC[A/G]GGGAAAAATGAAGGG | 7468 |
rs377427797 | snp | A/G | 0.00131314 | 0.0255899 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930975 | TATGAGAGCTATTCA[A/G]TGTAGTGCCTTCTGG | 7468 |
rs377444389 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911761 | ATGGATTAAAGAAAC[C/G]CATAAAAATAGTAGA | 7468 |
rs377444728 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970717 | AGAGCTGGGCTCTAG[A/G]GGCGGTTGAGGGAGG | 7468 |
rs377485810 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903092 | GGAGGATCAAAAAAA[-/A]CATGAAAATGTGTCA | 7468 |
rs377487778 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930914 | CAGCGGTCCAAGTGC[A/G]TGTGGTCACAGTAAA | 7468 |
rs377490567 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948296 | TTCCAAATGCATCTC[A/G]TTGGATATGGAATAG | 7468 |
rs377493814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903807 | TGGCGTGATCTCGGC[C/T]CACTGCAAGCTCCGC | 7468 |
rs377495411 | snp | C/G | 0.000295989 | 0.0121617 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918648 | AAGTTGTGTTTCATG[C/G]TAGCAAGTTTCAGAA | 7468 |
rs377547136 | snp | A/G | 3.5402e-05 | 0.00420711 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959424 | TGTGCAAGGGTATTC[A/G]GAAGGCTCTCATGTG | 7468 |
rs377563155 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875472 | TTTTATACAGACAGG[A/G]TTTCACCATGTTGCC | 7468 |
rs377599152 | snp | G/T | 1.64806e-05 | 0.00287054 | intron-variant, utr-variant-3-prime, missense | WHSC1 | GRCh38.p7 | 4:1942381 | TTGGATTTGAACCCA[G/T]CTGCTCTGTACTGCA | 7468 |
rs377606601 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931008 | TGTGGCTCCCTTGCT[C/T]TCCTACCCAAGTTGA | 7468 |
rs377608761 | in-del | -/CTGCTGAGATG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976211 | CCTGGAGCTGTGTGT[-/CTGCTGAGATG]CTGCTGAGATGCGTC | 7468 |
rs377614534 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899180 | TTCAACATTTTTTCA[A/G]GGTTTTACATTTGCT | 7468 |
rs377662920 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972260 | CAGTGTCACTGACGG[A/T]CACAAGAGATGATAT | 7468 |
rs377750558 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938401 | TCCTTTTTTTCTTTT[C/T]TTTTTTTTTTCTTTC | 7468 |
rs386670551 | multinucleotide-polymorphism | AAT/GAC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881786 | GATCTAGGTGCATAT[AAT/GAC]AGGGAGGTTATACCT | 7468 |
rs386670552 | multinucleotide-polymorphism | GG/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915984 | GGTACCTCCTTTCTT[GG/TT]ATTTTGGGCCCGTCT | 7468 |
rs386670553 | in-del | A/GTCTTG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937550 | AAAAGAAGTAATGGT[A/GTCTTG]TCTCTTCAGATTTGG | 7468 |
rs386670554 | in-del | ACC/TGGGT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957376 | GCAACCTCCACCTCC[ACC/TGGGT]TCAAGCAATTCTCCT | 7468 |
rs397738382 | in-del | -/A | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897186 | AAGGAAAAAAAAAAA[-/A]GGAAAGTGGTTTGGG | 7468 |
rs397829958 | in-del | -/A | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965075 | AAAAAAAAAAAAAAA[-/A]GCCTACAAAGAGACA | 7468 |
rs398063194 | in-del | -/AA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905142 | TCTCACAAAAAAAAA[-/AA]GAATGTTATATGTCC | 7468 |
rs527240655 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934950 | ATAATCCCTAAGGTT[A/C]GATATAGTCACCAGT | 7468 |
rs527280185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976987 | TGCTGTGGGGGCGGG[A/G]CGGCCAGGAAGGAGG | 7468 |
rs527314300 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981700 | CTTCGCAGTGTTTGT[C/T]TGTCTTGACATCTAA | 7468 |
rs527331376 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891229 | GAGAACAGAGGTTCT[A/G]CCATCATTCAGTGAT | 7468 |
rs527333950 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877918 | TCTGTGATCCTGGTG[C/T]TTTATGAAGCCAAGA | 7468 |
rs527351425 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981289 | CAGTGGAGCCAGGCT[C/T]TGGGGTAGCGGCCCT | 7468 |
rs527420365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902676 | ACTCCTGACCTCAAA[C/T]GATGTTCCTGCATCA | 7468 |
rs527424405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940948 | AGGGACTCAAACCAA[C/T]TCAGTGGTGGTCGAG | 7468 |
rs527440341 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932963 | CTGCCTGAGGGGGGC[A/C]TCGAGAGTTTGGCTG | 7468 |
rs527472497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940258 | AGATTTCTTTGTTCT[C/T]ATGCATTTCATGGCT | 7468 |
rs527483826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949216 | TGGGTGTTAAAGAAC[A/G]GGATGTGCGCTGTGG | 7468 |
rs527484574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948379 | AATGTGCCACCTCCA[C/T]AAATGGCTTCTCCGA | 7468 |
rs527517891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909013 | AATGGTAACTGGCTA[G/T]TATTGCACTTTCTAC | 7468 |
rs527546992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955517 | ATCATTTCGCAAACA[C/T]ACAGGAAATTATTTG | 7468 |
rs527567321 | in-del | -/AGAA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968621 | GAAATAATAGTAATT[-/AGAA]AGCACAGATTAAAAA | 7468 |
rs527581518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908510 | AGCAGTTCAGAAGGA[C/G]TCAAGCCTGGGTAGA | 7468 |
rs527646806 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921875 | AATATTAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 7468 |
rs527651510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921877 | TATTAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 7468 |
rs527654603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961863 | TGGGGAAGTGTGGCC[C/T]CCTTAGTGCCTGAGT | 7468 |
rs527658002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915256 | GTGTAGCTGAGGCTA[C/T]AGGCGCCCACCACCA | 7468 |
rs527690823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883861 | CCACATGGAGCTGCA[C/T]GCAGGAGCTGCGTTG | 7468 |
rs527691008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961325 | TCTTTCAGCTGCGCC[A/G]GAGGGCTAGAGCTAA | 7468 |
rs527692395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876644 | TGCAGTGAGCTGTGA[G/T]CATACCACCACACTC | 7468 |
rs527705950 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971541 | ACTTAGAGAACAGAA[A/G]CAATAGAAATAAATA | 7468 |
rs527722073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969935 | TATTTTCTAAGCAAA[C/G]CCTAAACCTCAAGGA | 7468 |
rs527759475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968902 | TTCACAGCCAAACAA[A/G]TCTATACATAGGATT | 7468 |
rs527801491 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958443 | AGCAAGATGGCGGGG[C/T]GGCAGGGGAGCTTGC | 7468 |
rs527812718 | in-del | -/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925415 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTTTTGC | 7468 |
rs527827224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927296 | CTATGTTATTGACTA[C/T]GCCGTAAGCAGTAGT | 7468 |
rs527835716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932831 | CTCATCCTGGATGAA[C/T]GGAGAGGTGCTCAGG | 7468 |
rs527860395 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895991 | TCTGCCTGGTGGTGG[C/T]TTCTTTTCCTCCTTA | 7468 |
rs527869987 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937512 | GTTTTATTAGCTCCT[A/G]TCTCAGGAGATAGCA | 7468 |
rs527898636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932528 | GAGGTGGGCAGATCA[C/T]CTGAGGTCGGGAGTT | 7468 |
rs527915149 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933365 | GGTGACAGCGTCCTT[A/C]AGGGCAACAGTGTCC | 7468 |
rs527935303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889129 | TCTGGAACTCCTGAC[C/T]TCAGGTGATCCACCC | 7468 |
rs527947221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895272 | TTCCTGCTTTTAATT[C/T]TTTTGGGTAGACAGA | 7468 |
rs527976165 | in-del | -/GTG | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973420 | CAGGGCCCTGCAGAA[-/GTG]GTGTGCATGCCAACG | 7468 |
rs528010618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900372 | TGGTATGACTGGAGT[A/G]TGCTGTCTTGACTGA | 7468 |
rs528047659 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885120 | TGTTTCAAAAAAAAA[A/T]AATAAAAATAAAAAA | 7468 |
rs528058770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919306 | GTTCTGAAGCTTCCA[A/G]TGCAGGATATGCTCA | 7468 |
rs528064659 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916599 | TCCCTGCCTCGGCCT[C/T]CCAAAGTGGTGGGAT | 7468 |
rs528086062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873884 | AGACAGGGTCTCTCT[A/C]TGTGGCCCAGGCTTG | 7468 |
rs528087683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958638 | TGATAAGTGTGTGCC[A/G]GAGGTCAGGTGCTCT | 7468 |
rs528090663 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943430 | AATAATAAAAATGAT[-/A]AAATTGCCATCATTC | 7468 |
rs528100344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966725 | GCTGGTATTGTAATT[C/T]AGTTTGTAAATTCTA | 7468 |
rs528147811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965756 | GAAGGTGAAGGGTAC[C/T]TTTGCACATGGCGGC | 7468 |
rs528152900 | in-del | -/ACTC | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946198 | AAGGTTTCTTAAAAT[-/ACTC]ACAAAGCTGTTATTG | 7468 |
rs528154215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925027 | GGCCTCCCTTCCCTC[C/G]CCTGGACTCTGGCTG | 7468 |
rs528156709 | snp | A/G | 3.38478e-05 | 0.00411373 | missense | WHSC1 | GRCh38.p7 | 4:1918565 | TCTCCATGCCACGAA[A/G]CAGGAAGGGAGATGC | 7468 |
rs528193290 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953318 | CCTTCTTTAACTTTT[C/T]GTTAGGGATTCACTC | 7468 |
rs528208523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917474 | GAGTTTCACTCTTGT[C/T]GCCCAGGCTGGAGTG | 7468 |
rs528225715 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883236 | AGGTTCAGAAACAAG[A/G]GAAAGCCCATTAAGA | 7468 |
rs528258530 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972648 | ATAAAGGCCAATTCC[A/C]GATGGATTGAACAGC | 7468 |
rs528263880 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924301 | TTGACAGCTAGGCCT[A/G]CGCAGGGTTGGTGAG | 7468 |
rs528278405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886211 | GCTGTTTCCTTTTTT[A/T]CTTTTTTCTTTTTGA | 7468 |
rs528306346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936173 | CAGAGTTTGCCTGGT[A/G]CCTGCAGGGGAGTGA | 7468 |
rs528321215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898431 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 7468 |
rs528337952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892177 | TTAGAGATGGGTCTC[A/G]CCATCACCATGTTGC | 7468 |
rs528343817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885802 | TACAGGTAGTTCCTC[A/G]CTGCTCTCTTCCCTC | 7468 |
rs528349572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898525 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCGCCT | 7468 |
rs528352933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930073 | CAGCCCTGGTGTGGC[G/T]GGAGGGTAGGGAAGC | 7468 |
rs528399118 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982586 | CGAGGGCTGATCCTA[C/T]CTGTTCCCCACCCTG | 7468 |
rs528421169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935676 | ACCAGCCTGGCCAAG[A/G]TGGTAATACCCCGTC | 7468 |
rs528435202 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943335 | TGTTGTAAACCATTA[A/G]GTAATGTAACGCATG | 7468 |
rs528498822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904057 | AAAATTTTGATGAAA[C/T]GATGTTGAGGCTATC | 7468 |
rs528517283 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950658 | GTTCCTTTACACATT[C/T]GTTTGGTGTTAGCAT | 7468 |
rs528572926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909874 | TCAACCTCCTGACCT[C/T]GTGATCCGCCCAACT | 7468 |
rs528586182 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878721 | GTGAGCATTTTGCCT[G/T]GATGTGGAGTTGGAA | 7468 |
rs528616882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872451 | GGTATTGTATAGGAC[C/T]CATTGCAGCACGAAT | 7468 |
rs528632133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957738 | TGGCTGTTCTCTGAG[C/T]ACTCCTTTGCCTCAC | 7468 |
rs528649300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917271 | AGATAACTTGTTTTA[A/G]AATTTATATATACAC | 7468 |
rs528673695 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870980 | CCGCGCGCCCAACGC[C/T]AGCCTCCGCGGCCGC | 7468 |
rs528683284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964631 | CAAAGAGGTGCGCTG[C/T]GCTGCCGTTGTTATC | 7468 |
rs528731821 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885124 | TCAAAAAAAAAAAAT[A/T]AAAATAAAAAAAATA | 7468 |
rs528754600 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878327 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7468 |
rs528764242 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873675 | TAATCAAATCTTACA[A/G]AGTTTACTCACATGG | 7468 |
rs528824082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922663 | AGGTGTGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 7468 |
rs528844340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924489 | TCCAAAGACCACCCT[A/G]TTGGCTTTTTGGGAC | 7468 |
rs528868205 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917980 | GAGATGGGGTTTTGC[C/G]ATGTTGACCAGGCTG | 7468 |
rs528896418 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964752 | TCATTTTTCTCTTTT[A/T]CCCCTTTTGGGAGCC | 7468 |
rs528928780 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925206 | CGGGAGTGCTGGTGC[A/T]CACAAGGATGGTTTT | 7468 |
rs528949987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885723 | CCTCTCTTGGTACCC[A/G]TGCACTGCTCCTCTT | 7468 |
rs528980531 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885480 | TAAAACTTCTGATAT[A/G]TTGATAAAACTTCTG | 7468 |
rs529006758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935585 | ACCTCTTTGGCCGGG[G/T]GTGGTGGCTTACGTC | 7468 |
rs529017211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930043 | TTTCTAGCATGCTCC[C/G]GGTGCTGATGCTGGC | 7468 |
rs529068807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943272 | GTTAATTCCCGGCAG[A/T]TTCTTTGGCTGTGTT | 7468 |
rs529079289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891985 | CTCCCCATTGCCCTC[C/T]ATGCTTTCTCTTTTC | 7468 |
rs529125165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898272 | TTGTATTTTTTGTTG[A/C]GATGGGCTCTCACTG | 7468 |
rs529135372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977076 | GCAGCCCAGAGGGGC[C/T]TGGCCTGGCTGCACT | 7468 |
rs529137247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904000 | TGGCCTCCCAAAGTG[C/T]TGGGACTACAGGCGT | 7468 |
rs529148650 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982525 | CTGCAGTCGGCTGAG[C/T]CGGGTGGTCCCCAGG | 7468 |
rs529152892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897621 | CCCGTCTCTACAAAA[A/C]ATTTTATTTTTATTT | 7468 |
rs529216137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950607 | GCAGCTGGACTGCAC[A/G]GTCACCTGATGAGGC | 7468 |
rs529219632 | in-del | -/ACTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933255 | CAGCAGGGCACGGAC[-/ACTT]ACTTGTACCTCTGCC | 7468 |
rs529264955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949852 | TGTTTTTCTTCCACC[A/G]CTCCCTGCAATGTCA | 7468 |
rs529277015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957117 | GGCTGACTTGGGGCT[A/G]CAAAAACAGGGCAGA | 7468 |
rs529296698 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909748 | CAGGTTCAAGCGATT[C/T]TCCTGTCTCAGCCTC | 7468 |
rs529319517 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870842 | GGCGGGGCCTCTGCG[C/G]CGGTTTCCCCACCCG | 7468 |
rs529347443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916553 | CTTTTGCCATGTTGC[C/T]CAGGCTGGTCTCGAA | 7468 |
rs529355998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956508 | ATCTGAAGGAAGGGT[C/T]CTGTTGTCTCGACCT | 7468 |
rs529401006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923133 | CCATGGGAGAGGGAA[A/G]GATTTCTTAAATAAG | 7468 |
rs529421245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922581 | GCCACATTTGAAGAG[A/T]GGCTTGGCCTGAGGA | 7468 |
rs529435827 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870264 | AGCCCGGGTAGCGCA[C/G]TTTCACAAAGCTCTC | 7468 |
rs529467952 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918060 | TGCTGGAATTATAGG[C/T]ATGAATCATGTGCCT | 7468 |
rs529488928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971268 | TCAGACAAGGCAGAA[C/T]TCAGGCCCTACCACT | 7468 |
rs529507385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891193 | GCCACTGTGCCCCGC[A/C]TACGTGGAATTGTTT | 7468 |
rs529552024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970727 | TCTAGGGGCGGTTGA[A/G]GGAGGGGGTCCAGGC | 7468 |
rs529559398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884097 | ATTAGATTTTTCTCC[C/T]TTTTTTTGTCGGGGA | 7468 |
rs529568284 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981201 | AATATGTTTCTCCCC[C/T]TTTCCAAAAACTGTT | 7468 |
rs529591378 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950876 | TTTTGAATTTTCTAC[A/G]TAGCCTAATTGACGG | 7468 |
rs529601791 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906901 | TCTGACCTCAAGTGA[A/T]CTGCCCACCTCGGCC | 7468 |
rs529606686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934181 | ACCTCCACCTCCTGG[A/G]TTCAAGCGATTCTTC | 7468 |
rs529677725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906621 | CTTCTCTGACATTCA[A/G]ATATACTGCCATTTT | 7468 |
rs529694134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953909 | CTGTCCTCTCGGGCT[C/T]AAGCTGTCCTCCTGC | 7468 |
rs529737678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906058 | CTCCACACAGCAAAC[A/C]CTGTGACTCCCATGT | 7468 |
rs529749735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913617 | CTCTCTCTCTGCCTC[A/G]GCTACCAAACAGGGA | 7468 |
rs529761088 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943240 | TGCTATTCACAGTAC[C/T]ATGCGAGTAGCCCAC | 7468 |
rs529771176 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980205 | TTTCACTTTAGTTTT[C/T]AAAAGGTCCAGTTCT | 7468 |
rs529778013 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978365 | GCGCTGGGGGACACT[C/T]CTGCACCCGGCACAG | 7468 |
rs529781802 | snp | C/T | 0.000204785 | 0.0101168 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918135 | TGTCTCTTTTTTTTT[C/T]CCCAGCTATTGAAAC | 7468 |
rs529891600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874915 | GAGAAAAAGACTTGT[A/G]TTGGTAACCCAGGGA | 7468 |
rs529892176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968152 | ATGGAGAGAGCTGAC[C/T]ATCAGTATAATTTAG | 7468 |
rs529911696 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971569 | ATAAATCTCTTCTTA[C/G]GAGCCCACAATAGTG | 7468 |
rs529914988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881348 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTTAC | 7468 |
rs529957566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973357 | CTGGGTTGTCCTGTT[A/G]GCATTGGTGGCATGT | 7468 |
rs529995829 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945815 | GCCACGGATTCCCCT[C/G]GCTGGAGAGGCTCCT | 7468 |
rs530016240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1893912 | GTGGTGGCACGAGGT[A/G]GGCATTTATTTTCCC | 7468 |
rs530036107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879292 | GGAGTGATCTCAGCT[C/T]GCTGCAAGCTCCGCC | 7468 |
rs530068260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937781 | GTCATTCCCTGGGCA[A/G]CGCTGCTCTAGTGCT | 7468 |
rs530068396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931186 | TTTCTTGCTTCTGAG[A/G]GCAATCCTCCTGGTT | 7468 |
rs530080247 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870259 | TCTATAGCCCGGGTA[A/G]CGCACTTTCACAAAG | 7468 |
rs530130823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937245 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTGG | 7468 |
rs530158472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898585 | AGGAGAATTGAACCC[A/G]GGAGGTGGAGGTTGC | 7468 |
rs530161011 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899038 | TGGGACAGTTGGTAT[G/T]ATATGAGCTGGAAGA | 7468 |
rs530225675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944274 | TTTCCTGAAGGAGGT[G/T]GGTGGAAACGGCTCT | 7468 |
rs530231905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951517 | ACACACACACACACA[C/T]ACACACAAAGTTCCT | 7468 |
rs530235750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959085 | GTCAGAGAGATGGGT[C/T]GGGAAGCTGCTCAGA | 7468 |
rs530244511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944881 | TGCTGTCTTGAGTAT[A/G]TATTTTATCTCTTAT | 7468 |
rs530266625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904670 | GATTGCTTGTTTCAG[G/T]ATGATTTGCAGCAAG | 7468 |
rs530293709 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958408 | CTGAGCCCCAAACAC[A/G]TAGATCCTGTACCTC | 7468 |
rs530375711 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879462 | CTGACCTTGTGATCC[A/G]CCCGCCTCGGCCTCC | 7468 |
rs530376712 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895104 | TCCATATTGAAGCAG[A/G]TATCAGCATTTCCTT | 7468 |
rs530428721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952510 | ATGGGCTTTTCATCC[C/T]GTGGGCTGGCCTGAG | 7468 |
rs530429234 | snp | A/T | 1.68576e-05 | 0.00290319 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918530 | AGTAGGGTCTCCTCC[A/T]GGGAGGAAGAAGACC | 7468 |
rs530516056 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893765 | GCCCAGGCTGGTCTC[A/G]AACTTCTGAGCTCAA | 7468 |
rs530523142 | snp | C/T | 0.000176445 | 0.00939102 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953118 | AGGTGAAGCTGGAGC[C/T]CAGATCGCAGCAAGG | 7468 |
rs530532030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959860 | TTTTTGGAAAAAAAA[C/T]TTTTTTTGTTTTTGT | 7468 |
rs530533885 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909765 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 7468 |
rs530537005 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949477 | CTTGGAAAAAGCCCA[C/T]TCTGGCTGGGTGCGG | 7468 |
rs530589151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967456 | GGTGGCGGGCGCCCA[C/T]AATCCCAGCTACTCA | 7468 |
rs530590807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925106 | ATGCTCTTTAACTGT[C/T]CTGTAATAAGCAATT | 7468 |
rs530604700 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947557 | TATAGTATTTTAGAT[C/G]ATGAGTGACTTATTT | 7468 |
rs530671302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908911 | CCTTGGCCTCCCAAA[C/T]TGTTGGGATTACAAG | 7468 |
rs530690634 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877327 | TCTTTCTAAAATACA[A/G]ATGTCCTATGTGTCC | 7468 |
rs530707928 | in-del | -/AAC | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882667 | GACCTCTGTCTCAAA[-/AAC]AACAACAACAACAAC | 7468 |
rs530721206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978059 | TTGAACCCAAGAGAC[G/T]GAGGCTGCAGTGAGC | 7468 |
rs530757422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973244 | ACATGGCGGGCAACC[C/G]ACAGATGAAAACTGG | 7468 |
rs530759720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930551 | TAAAGGGCCGTGCAT[C/T]TGATTTCATGCAAAA | 7468 |
rs530791003 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892759 | ATCTTTAGTAGGGAC[A/G]GGTTTCACCATGTTG | 7468 |
rs530803894 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979751 | TCTTTACCAGTTTCT[G/T]ATTTTTATTCTCAAT | 7468 |
rs530818687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931131 | TACATGATGTGGTAG[C/G]GTCAGCCTTCAGGCC | 7468 |
rs530859142 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946237 | TAACTTCTAAAATTT[-/G]GGGGGGTCTTGCATT | 7468 |
rs530867871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898387 | AATGGTTTCGTGGCC[A/G]GGTGCGGTGGCTCAC | 7468 |
rs530880568 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962872 | AGAATTGTCTTGAAA[C/T]AGCCCTAGAGCTAGA | 7468 |
rs530952292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944061 | ATGGGGGAACGTGGA[C/T]GGGAATGATAGTGTA | 7468 |
rs531017972 | in-del | -/GCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906003 | GGGTGTGTGTGAGGG[-/GCT]GCTAATTCTTTCTCT | 7468 |
rs531021168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872468 | ATTGCAGCACGAATC[C/T]TTCTGTGCCCACGAT | 7468 |
rs531040770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910725 | CCTACTGATTTGTTT[A/C]TTGCTTGTTCTATTA | 7468 |
rs531050266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911409 | CCTGGCCAACGTGAT[A/G]AAACCCTGTTTCTGC | 7468 |
rs531054419 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874105 | GCAGCAACAGAAGCC[A/C/G]TAAGGCTTTTTACTC | 7468 |
rs531084199 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879533 | CTACACACATTTTTT[A/T]AAAAATGTGTATTTT | 7468 |
rs531084407 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1871801 | GGCGGGAGGACCGGG[C/T]GGACCGCGGAGGCCG | 7468 |
rs531112574 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978589 | CACGATAATGTTGAA[C/G]TCGTGATTCCATCAC | 7468 |
rs531123092 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950793 | ATGTTCATAACACTT[C/G]CTTCATTTTAAGGAA | 7468 |
rs531130912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958331 | TGAGGGATGAGCCTC[A/C]CACCTGCACCAGGCT | 7468 |
rs531175363 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981178 | AAGGAAATAATGCAA[A/G]CATTTTAAATATGTT | 7468 |
rs531183832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896825 | TTCTTTCTTTCTTTT[A/C]CTTTCTTCTCTTCTC | 7468 |
rs531189933 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890713 | TTCCAGTGGTTCTAC[C/G]TCAGCCTCCCAAGTA | 7468 |
rs531222662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917879 | CGCTGCCTCCCAGTT[C/G]AAGTGATTCTCATGT | 7468 |
rs531249088 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973137 | GGTGTGAGCCACCGC[A/G]CCCGGCCGACATATT | 7468 |
rs531285574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940861 | CCTAGGCAACCTGGG[C/T]GGGGCTCATAGAGCT | 7468 |
rs531288897 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933531 | AGTAGCTGGGACTAC[A/G]GGCGCCCGCCACCAT | 7468 |
rs531348193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940185 | TGGGGTGGAAGGCGA[C/G]TCACACACCACACCT | 7468 |
rs531384748 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980762 | ACTGACTTGCTCGCG[C/T]GGCCGTGGCCTCTGA | 7468 |
rs531411887 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961761 | CGGGCCCTTCCAGGG[C/T]GGCTCCTTCAATGGC | 7468 |
rs531461878 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939527 | ATGATAGAAAGTTAA[G/T]CCAGAAGGACAAAGG | 7468 |
rs531486990 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933683 | ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCCTGCA | 7468 |
rs531526638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876516 | GGCAACATAGGGAGA[C/T]CCCATCTCTACAAAA | 7468 |
rs531530549 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910159 | ATAGCATTGTTGTAA[-/T]TTACAGCAGCAGAAC | 7468 |
rs531537433 | snp | G/T | 0.000646428 | 0.0179665 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955174 | AGGTAAAATGATGCG[G/T]TGTGTCCGCTGCCCC | 7468 |
rs531562791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915667 | GCTGCCTGCAACCAT[A/G]GGTGGGGAGGCTTGG | 7468 |
rs531602860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961287 | TTCAAACATCTGCAC[A/G]TTTTCTTCTGAGGTG | 7468 |
rs531619383 | in-del | -/AGAT | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972675 | AGCTAGGAGTGGGGG[-/AGAT]AGATGCATTTTATAA | 7468 |
rs531626945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915187 | GTGGCGCAGTCTCGG[C/G]TCACTGCAAGCTCCG | 7468 |
rs531628889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975197 | AGTACAGATACAAAA[A/G]TAATAAGAGTATTTT | 7468 |
rs531637188 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968292 | GTCTTAAATAAGTCA[G/T]GTTGTGTCAAATTAT | 7468 |
rs531639556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914651 | TACTTTTCTATCTTC[A/G]CACTTGATTGATGGT | 7468 |
rs531648553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921356 | TCCGGCTATGTGGGA[A/G]GCTGAGGCAGGAGAA | 7468 |
rs531651698 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936864 | TCTTTAAACTTGTAT[A/T]TGTAGTTGAGAGGAG | 7468 |
rs531665217 | snp | C/T | 0.000149614 | 0.0086478 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974637 | TCCTGTCCTCCCCGG[C/T]GCTCACTAAGGCTCG | 7468 |
rs531731408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882633 | CGCGCCACTGCACTC[C/G]AGCTTGGGCGACAGA | 7468 |
rs531751342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938708 | GTTCTCCTGTGGTTG[A/G]AAACTAAACTGTTTT | 7468 |
rs531773503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931900 | GGCTTATTTAAAAAT[A/G]AGCCAGCTCTTCCTG | 7468 |
rs531773597 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973456 | ACATCAGCACCGCGG[A/C]TCAGCGCGTCATGAC | 7468 |
rs531787658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888257 | TCTCCACTAAAAATA[C/T]AAAAATTAGCCAGGC | 7468 |
rs531788313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884510 | GTGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC | 7468 |
rs531794320 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889022 | TCTGCCTCAGCCTCC[C/T]GAATAGCTGGGATTA | 7468 |
rs531809676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946515 | ACCTCGTGATCCACC[C/T]GCCTCACCCTCCCAA | 7468 |
rs531809999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937907 | GTGACATGTTTTACT[C/G]ATGATCTTTGTTCAT | 7468 |
rs531820002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926479 | TTTAATTTTTTTTAT[G/T]TTTATTTTTGAGACA | 7468 |
rs531826079 | in-del | -/TTTG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925779 | ATATATATATTTTTT[-/TTTG]TTTGTTTGTTTGTTT | 7468 |
rs531842145 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979284 | AGGCTTTTCCCAAGG[A/G]TCGCTAGAAACTCGT | 7468 |
rs531854374 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937959 | TAAAAATTGGAAATC[C/G]TCAGTATAGTGATAC | 7468 |
rs531865030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906587 | CTTGGAGTTAAGTAA[C/T]TCCTGTAGTCTGCAA | 7468 |
rs531874809 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896404 | TGTAGCTAGACAAGG[G/T]CTTGCTGAGTCTGGC | 7468 |
rs531881505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932496 | TCCCGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 7468 |
rs531998006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899598 | TTGGAGCTTGTGATG[A/G]TGTACTCCTGAGAGA | 7468 |
rs532073059 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907729 | GCAATTCTCCTGCCT[C/T]AGTCTCCCAAGTAGG | 7468 |
rs532089202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939485 | ATTGTACAGTTTGTC[G/T]GCTTTTGTTTATGTT | 7468 |
rs532094524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906852 | TTTTAGTAGAGATGG[A/G]GTTTCACCATATTGG | 7468 |
rs532102070 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976083 | CCTCAGGTCACTGCC[A/G]CCCACCTGTGCCCAC | 7468 |
rs532114837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915017 | GATCTTACAGGTTGC[A/T]ATGGAAATAGGTATT | 7468 |
rs532169633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947457 | GAGACTCACCCCCAG[C/T]CCTGACCCTAGAATT | 7468 |
rs532185079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875576 | TTTAAAGAATTGATT[G/T]ATTTGATTACATTTG | 7468 |
rs532244078 | in-del | -/AGA | 0.00119737 | 0.0244387 | utr-variant-3-prime, cds-indel | WHSC1 | GRCh38.p7 | 4:1980458 | ACATCCATCTTGCAG[-/AGA]AGTTTACAGAACTCC | 7468 |
rs532281545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955087 | TCATGGAGGCTGAGT[A/T]ATTATTAGTTGCTCT | 7468 |
rs532302978 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927714 | ACAATGAGACTCTTA[C/G/T]CTCAGAAAAAAAAAA | 7468 |
rs532312626 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920130 | TGGGATCTGGAAATT[C/G]TGCCAGAGAAAGGCA | 7468 |
rs532317499 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874529 | TAAATGGGTATATGG[C/T]TTAGGGTAAACAAAC | 7468 |
rs532363229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974511 | GAGCCACTGCGCCCA[G/T]CCAGGGTGAGTCTTG | 7468 |
rs532367368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914481 | CGGGCACACGCCACC[A/G]TGCCTGACTAATTTT | 7468 |
rs532406496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968224 | ATGTCAGAAGTTAAA[C/T]GTGAGATCCAAGAAG | 7468 |
rs532431579 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920847 | GAGACCAGCCTGGGC[A/G]ACATGAAACCCTGTC | 7468 |
rs532435684 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942736 | GGCCCTGTTAGAGTT[G/T]CTTCTCCTCTAGTTT | 7468 |
rs532455437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926440 | TTACAGGTGTGAGCC[A/C]CCGTGCCTGGTTTGG | 7468 |
rs532472984 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906625 | TCTGACATTCAGATA[C/T]ACTGCCATTTTTACT | 7468 |
rs532489473 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898866 | GTTACAGTTGCTTCA[A/G]ACTCTCCTCAGTCAC | 7468 |
rs532514425 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896830 | TCTTTCTTTTCCTTT[C/T]TTCTCTTCTCTTTTC | 7468 |
rs532554486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937351 | GAGCCACTGCGGCTG[A/G]CCAGGTTACCTTCTA | 7468 |
rs532589753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953003 | CAGCTGCTCTCAAGG[A/T]GGAAAGGCCTCTTTT | 7468 |
rs532634893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931866 | ACTAAATTTAGAGAC[A/G]TGTTCCTTTTAAATG | 7468 |
rs532654420 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932568 | CCTGACCAGCATGGA[A/G]AAACCCCATCTCTAC | 7468 |
rs532672703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899506 | GTTCTAGTCCACGGG[C/T]ATCTCTGGTCCTTAC | 7468 |
rs532700980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945782 | TCTGGGCCTGAGACG[C/T]GCATGGAGGGCTGTA | 7468 |
rs532704104 | snp | C/T | 3.3151e-05 | 0.00407117 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952218 | GAGGTTCACCTGCAG[C/T]GAGTGTGCCTCAGGC | 7468 |
rs532785347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905783 | CCTGGCTTCAGCTCT[A/G]TCTCCATGGAGGACC | 7468 |
rs532787347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899244 | TTTTCTGTGGAGACT[A/G]CGGGTTGCAGACACC | 7468 |
rs532791083 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885447 | CGAGAGGGGGCCCTG[A/G]TCATTCTTGTAAGTT | 7468 |
rs532805767 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936737 | TGAGTAAAGCTTCAT[C/G]CTGTTTTTCACTGAT | 7468 |
rs532808382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971409 | GTGAATACAGCTGAC[A/G]GTGAGTTCACCTCTT | 7468 |
rs532823909 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875631 | AGATTGGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 7468 |
rs532832603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977003 | CGGCCAGGAAGGAGG[C/T]GACGCTGGGAACTAA | 7468 |
rs532851879 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905187 | AATAATGGTTGGTCA[A/C]CCCATAAATGTGTTT | 7468 |
rs532852601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891624 | TTGGGAGGCTGAGGC[A/G]GGCAGTTCACGAGGT | 7468 |
rs532894094 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981727 | CTAAACCCCGGCGTG[C/T]GCAGTGCCCATCTTC | 7468 |
rs532905102 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891774 | AGGCAGGAGAATGGC[A/G]TGAACACGGGAGGCG | 7468 |
rs532925216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942066 | ACATTTGTTTGAAAT[A/G]AGGTACTTTTATAGG | 7468 |
rs532928944 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923299 | CCACTTCAGCCTGGG[C/T]GACAGAGACCCTGGC | 7468 |
rs532932765 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934982 | TTTTTGTTGTAAAGA[G/T]ATTTGATCTGTAAGA | 7468 |
rs532979653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949817 | GAAGTCAGCAAACAC[G/T]TCTGTGTTAGTTTTT | 7468 |
rs532991383 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909262 | CTGTTTTTCCCACCA[-/C]CCCCCCCCAACCCTA | 7468 |
rs532999628 | in-del | -/TGG | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903341 | GGAGGAGTTTTTCTT[-/TGG]TGGAATGTTCAGCCT | 7468 |
rs533045883 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929445 | GTGCCTTCACTTGCC[A/G]AAGTCCACAGAACTA | 7468 |
rs533048062 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892572 | AACCACTGATAACTC[-/T]TTTTTTTTTTTGAGA | 7468 |
rs533089521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949270 | CCTCACAGTGACAGA[G/T]CCTTAAAGTGTGCAC | 7468 |
rs533128210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891329 | GTAAATCATATTTGC[A/G]AACTTGGGTTTTCCA | 7468 |
rs533139530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897603 | TGGTCAACAAGACAA[A/G]ATCCCGTCTCTACAA | 7468 |
rs533149918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956331 | TAGGAAAATGTTTGC[A/G]GTCTGGTTTATTTGT | 7468 |
rs533161633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955622 | GTAATAAGTGTAGAC[G/T]GTGAAGCACTGAATC | 7468 |
rs533170847 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870153 | GGACAGCAGCGGAGG[C/G]GGCGCGGGAGAGGAA | 7468 |
rs533198007 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981376 | GTGTGGCTGGCTCTC[A/G]GCCCTGCCCAGCTTT | 7468 |
rs533200589 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967451 | GGCGTGGTGGCGGGC[A/G]CCCATAATCCCAGCT | 7468 |
rs533246779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922510 | TAAATTCAGTATAAT[G/T]CTAATAAAACTTCCA | 7468 |
rs533321018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927765 | GCCGTGTAGGGAGCA[C/G]GCAGGATGAAGGAGG | 7468 |
rs533374982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878015 | GACTGGGTGGCAGTA[A/G]GACTCTGTCCCAAAA | 7468 |
rs533401626 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954506 | TAGCTGTGACCACGA[C/T]GCCTGGCTAATTTTG | 7468 |
rs533408191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890637 | ATGGAGTTTCACTTT[C/T]GTTGCCCAGGCTGGA | 7468 |
rs533417884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896192 | GCCATGACTCCTCTC[C/T]TTCGGGCTCTGTGCA | 7468 |
rs533439993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877418 | TTTCTGACTCTCACT[G/T]CACTACTTGTTTTGC | 7468 |
rs533469255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921743 | GCCAAAATCACGCCA[A/G]TGCACTCCAGCCTGG | 7468 |
rs533516134 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891382 | AGGAATGGGTTGGAG[C/T]TTGGTCCGTCTCACG | 7468 |
rs533537804 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877725 | TGCTCTGAAGCCCTG[C/T]AGCTCTGCTGCCTCC | 7468 |
rs533588016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884137 | GTCTTGCTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 7468 |
rs533599116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970170 | CACATTGGGCGACGT[C/T]GTAAGTAGGATTACT | 7468 |
rs533600548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883674 | CTCCGCTCTGCTGAT[C/T]CCACCTTGTTTGTTG | 7468 |
rs533617347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976146 | GGGTGGCGGGCGGGA[A/G]CTGTTCTGCCTGTGG | 7468 |
rs533634832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1890024 | CTGGCAGCCATTCTA[C/T]TTCTGTCTTTATGGA | 7468 |
rs533635865 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980734 | GGACCCAGGGGAAAC[A/G]AGCTGTGTAGCCACT | 7468 |
rs533644226 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980926 | TTGTTCTAGGGACAG[A/G]CCGGGCAGTGTCCCC | 7468 |
rs533653843 | snp | C/T | | | missense | WHSC1 | GRCh38.p7 | 4:1918526 | GAGGAGTAGGGTCTC[C/T]TCCTGGGAGGAAGAA | 7468 |
rs533672976 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980029 | TCTGTGGGTCTGGTG[A/T]TGGAAGATGCAGTCT | 7468 |
rs533699297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895781 | TTCTAGACCTGTTTT[C/G]ACATTTTTTGGTCTC | 7468 |
rs533769083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939564 | GAAGATTCATCTTTA[C/G]AACTTCACTTATTTG | 7468 |
rs533778699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895961 | ACAGACACTCACCTG[A/G]TGATGAGGAAGTCCT | 7468 |
rs533788291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928030 | AAGTAGCTGTGACTA[C/T]AGGCACTTGCCACCA | 7468 |
rs533802169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921725 | AGACGGAGGTTGCAG[C/T]GAGCCAAAATCACGC | 7468 |
rs533806790 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977987 | GAAAAATTAGCTGGT[C/T]GTGGTGGCGGGCGCC | 7468 |
rs533816254 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923073 | CGTGGTGCTGGGACC[A/G]CTGTGATTTATGAAC | 7468 |
rs533829978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877086 | AGGTTGAAATGAGCC[A/G]AGATCATGCTACTGC | 7468 |
rs533840492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901309 | AGTGAGCATGGCCAC[C/T]CTATGAGGGCACCTG | 7468 |
rs533845280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969517 | GAGACCAGCCTGGGC[A/G]ACACAGCAAGGCCTT | 7468 |
rs533865421 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894627 | CAGTGAGCTGTGATG[A/G]CACCATTGCATTTTA | 7468 |
rs533876936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947899 | TGAAGAGTAGGTGAG[C/T]GCTTTGCAGTCACAG | 7468 |
rs533930174 | snp | A/G | 1.64931e-05 | 0.00287163 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955234 | GGCAGCAGGATGCTC[A/G]GTGATCGCCTCCAAC | 7468 |
rs533946174 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897082 | GGCTGAGGCAGGAAG[A/G]TCACTTGAGCCTGGG | 7468 |
rs534005773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875823 | CTGAGGCAGGAGAAT[A/G]GCGTTAACCCAGGAG | 7468 |
rs534017227 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951525 | ACACACACACACACA[A/C]AGTTCCTGTTGGAAA | 7468 |
rs534054250 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919096 | CTTGAGTCCTGAAGG[C/T]GGGGTTTGCAGTGAG | 7468 |
rs534063555 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926181 | TTTTTTTTAAGACGT[A/C]GTCTCGCACTGTTGC | 7468 |
rs534078989 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932904 | TGGGAAAGCGAGGCG[C/T]GGGGCTGGCTTTGTG | 7468 |
rs534086438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926557 | CTCACTGCAACCTCC[A/G]CCTTCCGGGTTCAAG | 7468 |
rs534087983 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907937 | CATGATGGCTGGTAG[A/C]TTTCGTGGCACTGTT | 7468 |
rs534114811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960283 | TCTGATGGTTATTTT[C/T]ATGAAATGGAAGATC | 7468 |
rs534129769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939150 | TGGCTCTGTTTTTCT[G/T]GTTTTGCATGAGGTG | 7468 |
rs534154957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974656 | CACTAAGGCTCGGTC[C/T]TCTCCACGTGGTCCT | 7468 |
rs534196160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946958 | CATATAACTCTCGGG[C/T]AATATTTTGAAGCAT | 7468 |
rs534249086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932019 | GAGTTTCTGCCCACA[A/G]TGTGTGTCAGGTGTA | 7468 |
rs534270210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914681 | TTTGACTGGGTGTAG[A/C]ATTTTATGTTGAGAA | 7468 |
rs534318030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951590 | TGACATGCACACTGG[A/G]CAGGCCAGGCTGTGG | 7468 |
rs534329121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950931 | GATGATGGTTCCACT[A/G]TGAAATCACTGGCGG | 7468 |
rs534335479 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913999 | TGTATGGGAAGTAAA[G/T]TTGAGTCCTTGCAGT | 7468 |
rs534357758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920373 | GAGAATCACTTGAAC[C/T]GGGAGGCCACAGTGA | 7468 |
rs534375606 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882834 | TTTTCATGTCTCAGA[C/G]CTACTGCATCATGAA | 7468 |
rs534430978 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885978 | TAATCAGAAAATATA[-/TT]TTATGAATAATTTGT | 7468 |
rs534451681 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888442 | AAAAAAAAAAAGACT[C/T]TATATGCCAGAGAAT | 7468 |
rs534452102 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882127 | GGTTCCGGAAGAGTG[G/T]GTACAGAAGCCCAAT | 7468 |
rs534485755 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917466 | TTGAGATGGAGTTTC[A/T]CTCTTGTCGCCCAGG | 7468 |
rs534492189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957530 | TGACCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 7468 |
rs534498789 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978964 | GGCGGCCGGCCCTGC[C/T]TGCGGGAGAGGGCGA | 7468 |
rs534503823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872144 | GGGCGTTGGTCAGCG[C/T]GGACGCTCCCCCGGG | 7468 |
rs534558937 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957450 | ATCATGCCTGGCTAA[-/C]TTTTTTTTTTTTTTT | 7468 |
rs534575241 | in-del | -/CTGA | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982303 | GTGGGGCTCCCTGTC[-/CTGA]CTGTGTCATTTTGCC | 7468 |
rs534644965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929703 | GATGTTTTTCAGACA[G/T]TGAACAGAAACAGGT | 7468 |
rs534656548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928928 | ATGGCAGCAATCAGG[A/G]TAGGGCCTGCTGGGT | 7468 |
rs534689406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911115 | TCTGGCTTAGTTGAG[C/G]CCAGAGAGTCACAAA | 7468 |
rs534710622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973171 | ATAAAGGGGTCTGAT[A/G]TTTGGAATATCTAGG | 7468 |
rs534717731 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934613 | CCAGCACTTTGGGAG[G/T]CCGAGGCAGGCGGAT | 7468 |
rs534744304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891390 | GTTGGAGCTTGGTCC[C/G]TCTCACGGCCTGGCT | 7468 |
rs534795406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879978 | TTCAAGGTGAGGGCC[C/G]TTTGATATGTCTTCA | 7468 |
rs534800132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903129 | AGCTCATGCCAGGCT[G/T]CACCAGCATGCTTAT | 7468 |
rs534803781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897239 | GTAATCCCAGTACTT[C/T]GGGATGTTGAGATGG | 7468 |
rs534839603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941443 | ATGAGGCCAGTGTAG[C/T]GGGGTCGAGGCCTGC | 7468 |
rs534860310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902367 | GTAGTTGGACCACAG[A/G]TGTGCACCACTATAT | 7468 |
rs534869123 | in-del | -/TTTGGAAATCAAAATTTCC | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910095 | CTCAATCTAGATTCT[-/TTTGGAAATCAAAATTTCC]TTTGGAAATCTTAAG | 7468 |
rs534904536 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879986 | GAGGGCCCTTTGATA[G/T]GTCTTCAGTGCCTAA | 7468 |
rs534904878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949545 | AGGCGGGTGGATCAC[G/T]AGGTCAGGAGTTCAA | 7468 |
rs534941544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891805 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCATTG | 7468 |
rs534942116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885026 | GAGGCAGGAGAATCG[C/T]TTGAACCCGGGAGGC | 7468 |
rs534977786 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869804 | TCACAGGTGTGAGCC[A/T]CTGGCCTTGGCTCCA | 7468 |
rs535050286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897655 | TTGATATATTTTTGA[G/T]ACAGAGTCTCACTCA | 7468 |
rs535059908 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981928 | AGGTGTGAAATGCCC[C/T]GTCAGAAATTAAATA | 7468 |
rs535066596 | snp | C/T | 0.000395669 | 0.0140598 | missense | WHSC1 | GRCh38.p7 | 4:1978835 | AAGACTGAGAAGCCC[C/T]CCCCAGAGCCAGGGA | 7468 |
rs535082072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950324 | CCTGCGAGCAATTCC[A/G]CTCGCTCAGGGATTC | 7468 |
rs535086870 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872046 | GCAGGTTGGGGTCCC[A/G]GGGCCGGCGCCGGGG | 7468 |
rs535099930 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981557 | ACAGGGGGATGTGTC[C/T]GAATGGGCAGCTTAA | 7468 |
rs535131371 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977572 | CTGAGGTCAGGAGTT[-/C]CGAGACCAGTCTGAC | 7468 |
rs535146053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957447 | TGCCATCATGCCTGG[A/C]TAATTTTTTTTTTTT | 7468 |
rs535146660 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870464 | AGGAGCCGAACTTCC[A/C]TGGGCGGCGGGCAGC | 7468 |
rs535177708 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876433 | CAGTTGCTCATGCCT[C/G]TAATTGCAGCACTTT | 7468 |
rs535189593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963492 | AGCCCTAGGTCTGTG[C/T]CTTATGTTTTGGAGT | 7468 |
rs535189603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971589 | CCACAATAGTGCCGT[A/G]TACTTTTCAGAGGCA | 7468 |
rs535228976 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870357 | TGTAAAGCTCGAGCA[C/G]ACACTAAGGCTCAAG | 7468 |
rs535231252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949015 | TGGGTCAGCTTGGGC[A/G]ACTGTGTGGGTGACT | 7468 |
rs535248180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922826 | AGCTACTCGGGAGGC[C/T]GAGGCTGGAGAATTG | 7468 |
rs535305495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928809 | GGAGGTGAGAGGCAG[A/G]TGTGTTGTGGATCCG | 7468 |
rs535308440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916642 | GGACTGCGCCTGGCC[C/T]GGTTGGCTTTCTTTC | 7468 |
rs535308639 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919528 | TATGTTACTTGGAGT[A/G]GATCATATTCTCATG | 7468 |
rs535309000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963237 | TGGGTTTGTACACAG[C/T]GCCTCTAGGACCATG | 7468 |
rs535311084 | snp | A/C | 0.000694536 | 0.0186222 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955864 | GGTGTGAGACATAGA[A/C]TCGTATGCTTTTATG | 7468 |
rs535332167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884970 | TAAAAATTAGCCAGG[C/T]GTGGTGGCGGCAACC | 7468 |
rs535351752 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908291 | GCTTTGGCCCTTTAC[C/T]AAAGATCTGTGTACA | 7468 |
rs535373715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976794 | TGCAGGCACATCAGG[C/T]GCTCATGCAGCGAAG | 7468 |
rs535405733 | snp | A/C | 1.67719e-05 | 0.0028958 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957902 | ACCTGTATTTACTAA[A/C]ATCTTTACTCCTATT | 7468 |
rs535502670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879130 | CCCTAGATCTTGAGC[A/G]TGGCATGTGGTTCCT | 7468 |
rs535551991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910279 | CACCCAGGCTGGAGT[A/G]CAGTGTCACAATCTC | 7468 |
rs535575120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902255 | ATTTATTTTGAGATG[A/G]TCTCTGTTGTCCAGG | 7468 |
rs535576225 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923371 | CACCATCGACACAGT[G/T]AAAGGACAAATTCTG | 7468 |
rs535588630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908608 | CAAAGAGAAGTGAGG[A/G]AAGGACAGAGTGCTA | 7468 |
rs535590199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929609 | AGCATGGGAACAAAT[A/G]CATGGGGCTGACATC | 7468 |
rs535649974 | snp | C/T | 2.27918e-05 | 0.0033757 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955680 | GCCTGGCCGCCTCGC[C/T]CTCCTCTTGCAGGGG | 7468 |
rs535701576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891360 | TTTCAGTCTTTTCCG[C/T]CCCCGGAGGAATGGG | 7468 |
rs535740141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876884 | CTCACGCCTGTAATC[C/T]CAGTGCTTTGGGAGG | 7468 |
rs535763502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897177 | TCTGTCTCAAAGGAA[A/G]AAAAAAAAAGGAAAG | 7468 |
rs535783194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921655 | GCTGTGGTGGCGAGC[A/G]CCTGTAATCCCAGCT | 7468 |
rs535836875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931495 | TTGAATGTAAAAATA[A/C]CTGACATATTAGGGT | 7468 |
rs535836900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938152 | TGCAGCGGGTCTTGG[C/T]GTGGCCCCACCCACC | 7468 |
rs535872405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945977 | CTCTGGCCAGGTAGA[C/T]TTTTGTATACAGACC | 7468 |
rs535882047 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980977 | GGCCCCAGGGCCCCG[C/T]TGTCACTTGCCCAAA | 7468 |
rs535886615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896420 | CTTGCTGAGTCTGGC[A/G]TGCAATAGTGTGGTC | 7468 |
rs535889265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959826 | TTGTGGTGGTTTTGT[A/G]GTCATGTGAGAATGG | 7468 |
rs535894817 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948088 | GAATGTATTTCTAAG[A/G]CAAATAGGCAACTTG | 7468 |
rs535911075 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979423 | ATTACTCTGCTCTTT[A/G]GAAATGGCTGTATCA | 7468 |
rs536012797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912713 | CCTTCCTTACTACTT[A/G]GATTTTCTTTCTTTG | 7468 |
rs536022141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908013 | CACCAGCCGCATTTC[C/G]GGAAACATCACATCA | 7468 |
rs536034201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904976 | TCTCTACTAAAAATA[C/T]AAAATTAGCCGGACG | 7468 |
rs536047941 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869664 | GCACTGGCCGTAATT[C/T]TAAAAATTCATTTAT | 7468 |
rs536052000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877658 | GCTCTTGTCTTTTCC[A/G]TCGTCACCCACTCCC | 7468 |
rs536063567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874092 | AAATAATTAATCAGC[A/G]GCAACAGAAGCCATA | 7468 |
rs536096462 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962188 | CAGTGGAGCCTGCTC[C/T]GGGGGAGCACTGGGC | 7468 |
rs536125575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911909 | ACATGTAAGGAGCAT[A/T]TATCTGTGTCATTAT | 7468 |
rs536133716 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910622 | CCTCCTTGCTTTATA[C/T]AGGAAAAAAAATGCT | 7468 |
rs536141179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919496 | AGGAGTTGGGTTCCC[C/T]ACTTCCCACTTTTGG | 7468 |
rs536149751 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976292 | TGTTCAGCTTTTTCA[C/T]GCTGAGTCGAGTGAG | 7468 |
rs536152473 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964661 | CACACCTCCCTCAGT[C/T]GTTACAAGCCCCTCC | 7468 |
rs536163120 | in-del | -/CTTCAGGGCTGGT | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881097 | GTGGTTACATCAGGA[-/CTTCAGGGCTGGT]CTAGGTTGAGAGTGG | 7468 |
rs536170276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969315 | GGTGAGGAGACCTCC[A/G]TCAAGCCGACAGCAG | 7468 |
rs536172481 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914886 | TGTGCCCTGCTGTGG[A/G]TGTTGCAGTGGGACA | 7468 |
rs536209813 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960354 | CTTGGGAGCACTCAC[C/T]AGCAGGCGTAAGGAG | 7468 |
rs536275243 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928977 | AGTAGGCATATGCAG[C/G]GCTGGGGACAGGGAC | 7468 |
rs536284872 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893587 | GACAAGGTCTTGCTC[C/T]GTACCCCAGGCTGGA | 7468 |
rs536286189 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886082 | TTATCTTTTCCTTTA[C/T]GAAACTAAAGCGCGT | 7468 |
rs536310262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945421 | GTGTGTGTGAGGCTG[C/G]CAGAACAAGTGCTGG | 7468 |
rs536310845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972300 | GCGGTACAGGCTATG[C/T]CTCAGCTGGGAAAGG | 7468 |
rs536338199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902552 | TGAAGTGCCCACAGC[A/G]GTATTGAACCTCATG | 7468 |
rs536345758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899352 | GCGGGCATCCTGTGC[A/G]TTGCAGGAGATGCAG | 7468 |
rs536357869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905304 | CGATGTGGCGAGTGC[G/T]GAGTTAGAACTGAGC | 7468 |
rs536375753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930330 | CTGGGTCTTAAGTGA[A/G]TTAGTGGTTTTGGAA | 7468 |
rs536423313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952608 | GGTAACCTGGTTGGT[C/T]ACCGAACACTGAAGT | 7468 |
rs536491073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976844 | GAGCCTTTCTTTGTT[C/T]CACCAGCCGCACATT | 7468 |
rs536554371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973791 | ATCCCTGTTCACACA[C/T]GTGGTTTTGTTTGAA | 7468 |
rs536556131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903860 | CTGCCTCAGCTTCCT[A/G]AGTAGCTGGGATTAC | 7468 |
rs536632791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936771 | AGTTAAAATGCTCTT[C/T]TTATTTCAAAGAATG | 7468 |
rs536635158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966243 | TGAAAGGATACCATA[C/T]AGTCACTACAAGTTG | 7468 |
rs536651955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944407 | AATAATGGTGATACA[G/T]TCTAGCCTTAAGACA | 7468 |
rs536667286 | snp | C/G | 4.96857e-05 | 0.00498401 | missense | WHSC1 | GRCh38.p7 | 4:1930670 | TGAGGAGATTGAAGA[C/G]CTGCTCAGGTCACAG | 7468 |
rs536677407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898020 | TTTTGCCTTTTTTTT[C/T]CCCTCCTCCTTCTGG | 7468 |
rs536692761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965248 | GTCAAGAAAATCATG[C/T]ATGAACAAAATGGCA | 7468 |
rs536714101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978220 | CCATGGGTGCGAGAG[G/T]GTGGTCCCTAACGTG | 7468 |
rs536715117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951667 | CCAGGCCACCTACAC[C/T]CTGTGCTTCAGTCCC | 7468 |
rs536716634 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947127 | GTCCTTCGCAGACAG[C/T]GCACAGCCTGCTGTC | 7468 |
rs536725672 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907125 | GATAATGAACTTAAT[C/T]TCGCTAAGCTTCAGT | 7468 |
rs536728003 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873315 | GATTTTATTTTAAGA[A/G]TATGAGGTAATTAAC | 7468 |
rs536767625 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875501 | CCCAGGCTGGTCATG[A/T]ACTCCTGGGCTCAGG | 7468 |
rs536808736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911158 | TAATGGGCTGTGATG[A/G]GGAAAAAAGGAACAC | 7468 |
rs536815550 | snp | G/T | 0.000412156 | 0.0143495 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918700 | GCAGAATCATCTGTT[G/T]CTCAGCATTATCAGG | 7468 |
rs536833617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935814 | TGCTGTGAGCTGAGA[C/T]CATGCCACTGCACTC | 7468 |
rs536844135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943559 | ACACTGGATTTGTGT[A/G]TGTGGCGCTTTAGGG | 7468 |
rs536844224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935382 | GCACCCAGCTCCTTC[C/T]AGGCTGGTATTCAGC | 7468 |
rs536872048 | in-del | -/TGAG | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982159 | TTGGAAAATTGTGTA[-/TGAG]TGAGTATTTTTGTAT | 7468 |
rs536886582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898398 | GGCCAGGTGCGGTGG[C/T]TCACGCCTGTAATCC | 7468 |
rs536914114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942818 | AAACTAACAGCACAC[A/G]TTAGGAGGAGTCCTC | 7468 |
rs536914780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950901 | TGACGGGTTATATTA[C/T]CACAAAAACCAGTTG | 7468 |
rs536950010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904139 | TTGGACATTGTAGCC[C/T]GGTGAATCCTTGGTC | 7468 |
rs537049559 | in-del | -/TTTTTTC | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886206 | TTTCAGCTGTTTCCT[-/TTTTTTC]TTTTTTCTTTTTGAG | 7468 |
rs537074809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929749 | GCTGGCTGGCATTAG[C/T]GTGTCAGCCCTGTGC | 7468 |
rs537076556 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973864 | ACGCGGTTGTGCGGT[A/G]GATCTGGCGGCTCCT | 7468 |
rs537078409 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971929 | TAAAAGACATCAGCG[A/G]CTGCCAGCTGATGCT | 7468 |
rs537133835 | in-del | -/ATTA | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946260 | TTGCATTTATTTATT[-/ATTA]ATTTATTTATTTATT | 7468 |
rs537138095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904859 | TGTACGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 7468 |
rs537152501 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911783 | AATAGTAGAAAATTC[G/T]GTTATGTTATCCGGT | 7468 |
rs537165893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897792 | CCACCAAGCCTGGCT[A/G]ATTTTTGTATTTTTA | 7468 |
rs537231958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873584 | ATAGGTAGAAGACAA[C/T]CCACTCCTCCTAATC | 7468 |
rs537246215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872731 | TGCTTCACAGACTTT[A/C]AAGCCTTGATTTTTA | 7468 |
rs537272246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897345 | AAAAAGTTAGCTGAG[C/G]ATGGTGGGGTGCACC | 7468 |
rs537283972 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943408 | TTGTGACAGTAATAA[C/T]GGTTATAATAATAAA | 7468 |
rs537307367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880165 | CAAAATTCGGAGTTG[G/T]TGTAATCTTTGTAGA | 7468 |
rs537337698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903198 | GAAAACTGAGGCCTG[A/T]GGCAGTGGAACAATT | 7468 |
rs537376883 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948574 | TGGTGGGAAAAAGTC[-/G]GAATCTCTGCAATCT | 7468 |
rs537394499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927478 | ATCCCAGCACTTTGG[A/G]AGGCCATGGCGGGCA | 7468 |
rs537399989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921199 | ATGGTGGCTCACACC[A/T]GTAATCCCAGCACTT | 7468 |
rs537419243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879326 | TGGGTTCACACCATT[C/T]TCCTGCCTCAGCCTC | 7468 |
rs537427801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885834 | GGACAAGTTCCAGGC[A/G]CAGGAATGATATAGA | 7468 |
rs537470473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971697 | AGGGTGTGTGCCAGC[C/T]GGTGGGGTGCACCTG | 7468 |
rs537475765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935745 | GTGCACCTGTAATCC[C/T]AGCTACTCAAGAGGC | 7468 |
rs537489041 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977745 | TGCAGAAAGCTGAGA[A/T]AGCACCATTGCACTC | 7468 |
rs537528714 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980216 | TTTTTAAAAGGTCCA[C/G/T]TTCTACAGAGTGAGA | 7468 |
rs537537071 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982656 | CCCCGTCCTGATGGC[C/T]GCCTAGGGAGGGACT | 7468 |
rs537619996 | in-del | -/T | 0.00520309 | 0.0507392 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906655 | TTCTCTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 7468 |
rs537639304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942623 | TCATAATAGAAACAC[A/G]TTCATATTCCAGTGG | 7468 |
rs537645421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941714 | TTTAAATTACTGGGT[C/G]TTTTCCATTAAACTA | 7468 |
rs537649878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1950118 | TAACATCAAATAAAA[A/C]CCAAATTTTTTAAAC | 7468 |
rs537672966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900539 | AGAAAATCAGACCCC[A/G]CAAAGCTGTAGAGGT | 7468 |
rs537707149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949619 | TACAAAAAATTTAGC[C/T]GGACTTGTTGGCAGG | 7468 |
rs537713090 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935100 | CTTCAAATGCAGCTT[C/T]TGGAGTGGTTTTCAT | 7468 |
rs537737216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900156 | GTAACAGGAGGGATT[A/G]GGATGAGCTCTTTTC | 7468 |
rs537738353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906913 | TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 7468 |
rs537741491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910008 | GAATCCGTGTATCTT[A/T]GTAATATACTTAAAT | 7468 |
rs537751976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939163 | CTTGTTTTGCATGAG[A/G]TGCTTGACTGGCTTT | 7468 |
rs537821829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876088 | GGCATGGTTGCAGTG[C/T]CTGTAGTCCCAGCTA | 7468 |
rs537879911 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928779 | CAGGCCCGTGAAGGA[A/G]TGTGCTGTGTTTGAG | 7468 |
rs537888552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883072 | AGTAAAATTGATAAG[C/T]TGTGTTGTTTGGGAT | 7468 |
rs537929961 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922191 | AATAAATAAAGCTGT[C/T]ATTGTTTGCAGAAGT | 7468 |
rs537931913 | snp | A/G | 0.000148301 | 0.00860978 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974829 | TAACATGCGATTGCT[A/G]ACACTTGACCGAATA | 7468 |
rs537940690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912962 | AGGCTGTTCCAGTAT[A/G]ATAAAGAAAATACTT | 7468 |
rs537948183 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969731 | AAACAAAATCCTGAC[A/C]CAAAACAGCAGAACT | 7468 |
rs537959078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973881 | ATCTGGCGGCTCCTC[A/T]GGTGGAGGCCGGGGC | 7468 |
rs537965668 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891871 | CAAAAAAAAAAAAAA[A/C]CAAAAAAAAACAAAC | 7468 |
rs537970674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932606 | ACAAAATTAGCCAGG[C/T]GTGGTGGCACATGCC | 7468 |
rs538003691 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925782 | TATATATTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 7468 |
rs538038976 | snp | A/G | 1.65302e-05 | 0.00287486 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938493 | AGAACAAGCTCTTAC[A/G]AGGCCATGGAGGCAG | 7468 |
rs538106332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946143 | GATAAAGCTAAATTA[C/T]AGTCTTTTGCCAGAG | 7468 |
rs538112929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886559 | ACTTGCGGCTGGGCG[C/T]GGTGACTCACGCCTG | 7468 |
rs538114385 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897410 | GGATTGCTTGAGCCC[C/T]GAAGGATAGAGGTTG | 7468 |
rs538121908 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873142 | AGCCACCCAAACCCA[A/G]CAACCTTCAGTTTTG | 7468 |
rs538137832 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935461 | GGTTCTTACCCTCCA[A/G]GGGTGTTATCACAGA | 7468 |
rs538168854 | in-del | -/TTAA | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916695 | TGAGTCTCTTGTAAG[-/TTAA]TTAGTTTCCCTCTTT | 7468 |
rs538178863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978332 | AAATCAGCACAGCAG[C/T]CCCTGCCTGTCCACG | 7468 |
rs538182376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930903 | GGGGTTTGGGCCAGC[A/G]GTCCAAGTGCGTGTG | 7468 |
rs538205575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913858 | TTTCTACCATCTCTC[A/G]TCTCCACACACGAGG | 7468 |
rs538208058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925977 | CTGGCTAACTTTTCT[A/G]TTTTTTATAGGGATG | 7468 |
rs538213515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932558 | TTGAGACCAGCCTGA[C/G]CAGCATGGAGAAACC | 7468 |
rs538218833 | snp | C/T | 0.000807003 | 0.0200711 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953320 | TTCTTTAACTTTTTG[C/T]TAGGGATTCACTCAT | 7468 |
rs538271419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932169 | TGTCTGGGCACGGTG[G/T]CTCACACCTGTAATC | 7468 |
rs538330126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920231 | AAGGTGGGCAGATCA[C/T]CTGAGGTTAGGAGTT | 7468 |
rs538333033 | in-del | -/TTA | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973547 | GTTGATTAGTGCATT[-/TTA]TTATTGTGAAAAGCA | 7468 |
rs538341690 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930544 | TAAGTTCTAAAGGGC[C/T]GTGCATTTGATTTCA | 7468 |
rs538413265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881509 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 7468 |
rs538447754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931337 | CCTTCCTAGGCCTTC[A/G]GCTTAAAAAAACCAA | 7468 |
rs538452104 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955423 | CTCATTCCTTGTCTG[C/T]GCTGTGTTCATTGAT | 7468 |
rs538462699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945549 | GATGATAAGAAAGTG[A/C]TCCTGAGAAGGCTCT | 7468 |
rs538474502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887254 | GTGGCTGGTTCCATG[A/C]GGGAGGAAGTGAGAT | 7468 |
rs538475851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899399 | AACCCATCAGAGGTC[A/G]GGGTCCGCCCCCTAG | 7468 |
rs538482812 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892021 | ATATCTACTCTTCCT[A/G]TTTTCTGCCTCTCTC | 7468 |
rs538497124 | snp | G/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893553 | TTTTTGTTTTTTTTT[G/T]TTTTTTGTTTTGTTT | 7468 |
rs538516664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978583 | TTCAACCACGATAAT[C/G]TTGAAGTCGTGATTC | 7468 |
rs538528013 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960040 | TAATTTTATTTTTTT[C/T]TGGAGATGGGGTCTT | 7468 |
rs538588475 | in-del | -/TTTC | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900593 | TAAATGTAATTGCTT[-/TTTC]TTTCTTTTTTCTTTT | 7468 |
rs538650516 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880062 | TATTCTGTTTTCCTA[A/G]TGATTTTTATTTCAT | 7468 |
rs538667942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888513 | TATCATTTAGGTTGG[C/T]AATGATTTTTTCCTC | 7468 |
rs538679524 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979523 | CAGGTGGTGGCAGCA[A/G]TGGTGTTGTAAGATT | 7468 |
rs538680820 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888016 | CATCATCTTCTGCGA[G/T]GGACCATCTGTTTTT | 7468 |
rs538682823 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939010 | AAAATAAGAGGGGAA[A/G]TTACACTTCCTTTTA | 7468 |
rs538694536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881424 | CACGCTGCCACGCCC[A/G]GTTGATTTTTTTGTA | 7468 |
rs538706056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873666 | TTCTAAAAGTAATCA[A/C]ATCTTACAAAGTTTA | 7468 |
rs538708974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880786 | GAAAAATGAAGGGGA[C/T]TGATGACAAGAGACT | 7468 |
rs538715977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966346 | TAACTCCATTTGTTT[G/T]TTTGTTGTCTGCATG | 7468 |
rs538719785 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979057 | GGAGGGAGCGCCTCC[C/T]CACCACTGAGCCATC | 7468 |
rs538736670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918918 | TTTGGGAGGCCAAGG[C/T]GGGAGGATTGCTTCA | 7468 |
rs538748681 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933797 | TTAAAATAAACATTG[A/G]CATGTTGAAATTAAT | 7468 |
rs538752170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978515 | TCTGCCCGTCCTGTT[C/T]GCTGGAGCCAGCACT | 7468 |
rs538762025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972966 | CAAGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 7468 |
rs538768933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886531 | TTTCTATTTATCTGT[A/G]CTTTAAAAAGTAACT | 7468 |
rs538893690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970388 | GCTACAGAGATGCAG[A/G]TTGGAGCATAGAGAA | 7468 |
rs538905424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952809 | GACACCTGCACAGCC[A/G]TGGCCCTTCCTGCCT | 7468 |
rs538930147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912792 | AGAATCTTCCTTTTT[C/G]CTGCTTGATTCTGGT | 7468 |
rs538971797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898439 | GGAGGCCAAGGCGGG[C/T]GGATCACGAAGTCAG | 7468 |
rs538985533 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898590 | AATTGAACCCGGGAG[A/G]TGGAGGTTGCAGTGA | 7468 |
rs538991394 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919552 | TCTCATGCTTAAAAG[C/G]CTTTTTTTAAGTGTT | 7468 |
rs538996096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936052 | TTCATGTTATTGTTT[A/G]CTGAATGGGAATACT | 7468 |
rs539007810 | snp | A/G | 3.53982e-05 | 0.00420688 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959420 | TGGGTGTGCAAGGGT[A/G]TTCGGAAGGCTCTCA | 7468 |
rs539042957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956824 | CGCTGTGTTGCAGCC[A/G]GGTCAGTGCTGGCTC | 7468 |
rs539048220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878344 | AACTCCTGACCTCAA[A/G]TGATCTGCCTGTCTT | 7468 |
rs539069170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967158 | GAACAACTGTACTCC[A/T]GTAAATTGGATAACT | 7468 |
rs539087390 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934457 | GAGATTGTGCCATTA[C/T]ACTCCAGCCTGAGCT | 7468 |
rs539102686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970993 | ACTTTTTAAAGGACT[G/T]CCAGATTGGATCATA | 7468 |
rs539104335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963452 | TCTGGGGAGGAGGGC[A/C]GGGAGGTTATTTGTT | 7468 |
rs539117188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925246 | GTCAGTTAACCAATG[A/G]CCAACCCTTGAGGGA | 7468 |
rs539207944 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892066 | CACCTCAAGAATAAG[A/G]AAGGCATTTTGTTTG | 7468 |
rs539235175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884226 | TCAGCCTCCCAAGTA[C/G]CTGGGACTATGGGTG | 7468 |
rs539240398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936600 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 7468 |
rs539256697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892952 | CTCAAATATTTTCAT[C/T]TTTTTTATAATGGTC | 7468 |
rs539279442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933686 | GGTGTGAGCCACCGC[A/G]CCCGGCCCTGCAAGA | 7468 |
rs539292956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976184 | CTTTGCCAGTGGGTC[C/T]CATCAGCAGATCCTG | 7468 |
rs539295371 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890787 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 7468 |
rs539339410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958943 | CTGCTTTGTTATTTG[A/G]TTGCTTGTCTTTCAC | 7468 |
rs539351216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944333 | GGCTTGCCAAGAGTA[C/T]AGAAATTCATTATGC | 7468 |
rs539388425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940350 | CATTGTAATATGACT[C/G]CTGTGTTCTGGACTT | 7468 |
rs539442427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948571 | GTGTGGTGGGAAAAA[G/T]TCGGAATCTCTGCAA | 7468 |
rs539456521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947988 | AGTTGGCTGGAATGT[A/G]TTCACTAGGTTCCGT | 7468 |
rs539469758 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956474 | AATGTTCCATGGCTT[A/G]CCTTTATGTAAAATG | 7468 |
rs539475906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962665 | GAAATTTTTTTACTC[C/G]TAGGTTTTGTTGTTA | 7468 |
rs539484219 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884835 | CTGCCTGGGCTGGGC[A/G]TGGTGGCTCACGCCA | 7468 |
rs539496478 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916125 | CTGAGGCCACTGATG[A/C]TCCTGTCACTCTAGC | 7468 |
rs539554597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915324 | TTTCACCGTGTTAGC[C/T]AGGATGGTCTCGATT | 7468 |
rs539579784 | in-del | -/TTGCAAACCAAA | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968035 | GTGGAGCATCTGTAC[-/TTGCAAACCAAA]TTGGCAGCATATTAA | 7468 |
rs539589863 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922252 | AAATCTTTTAGAATT[A/T]ATAGAGTTCACCAGG | 7468 |
rs539589905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928781 | GGCCCGTGAAGGAAT[A/G]TGCTGTGTTTGAGGA | 7468 |
rs539629659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954362 | TTAGGCCACTGCTCT[G/T]ACCTCTTTTCTTTTT | 7468 |
rs539637924 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926044 | CTGGCCTTAAGCGAT[C/G]CTCCTACCTCAGCCT | 7468 |
rs539648507 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939201 | AGTTAAACAGACTTT[-/A]AAAAAAAAAAAAAGA | 7468 |
rs539670675 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890495 | TTTAGTAGAGACAGG[G/T]TTTCACTGTGTTAGC | 7468 |
rs539690508 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969123 | AGCACCTGGGGCCTG[C/T]CCCCAGCGGCGCTGA | 7468 |
rs539699242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896352 | CCCTTTTCATTTCTA[A/G]ACCTGGAGATTCTCT | 7468 |
rs539743018 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980574 | TGAGAGTGGCTACTC[C/T]GTGGTTTTGTGACCT | 7468 |
rs539755510 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933206 | GCATTGGGCTCAGGC[C/G]TAGACCTGAGGTGAG | 7468 |
rs539760137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902159 | GAGGGTTAAAAAAAC[C/G]TTTTTTGATTACTCA | 7468 |
rs539761981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896078 | GAGTGGTAGAGGCTC[C/T]TGGCCGGGGTCCCAC | 7468 |
rs539766727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889152 | ATCCACCCGCTTTGG[C/G]CTCCCAAAGTGCTGG | 7468 |
rs539789168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926572 | GCCTTCCGGGTTCAA[A/G]CGATCCTCCCCCCTC | 7468 |
rs539810468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907593 | CTCCACCTTGAAACA[A/T]CTTGTTCTACCTGTT | 7468 |
rs539819179 | snp | G/T | 1.65231e-05 | 0.00287424 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939666 | CAGCAACGAAAAATC[G/T]GTCTGATGCATGTAA | 7468 |
rs539872901 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901682 | CTTCTTAAGTCTGCA[C/T]CATCTGATGAGTGGG | 7468 |
rs539886262 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948465 | CTGTGGGACGCCCTC[A/G]TACTTTGCTCTCCTT | 7468 |
rs539895038 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889829 | TTTTTTTTTAATTGA[C/G]ATAAAATTCACATAA | 7468 |
rs539909851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876170 | AGTGAGCTGAGATCG[C/T]GCCACTGCCCTCCAC | 7468 |
rs539920669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914989 | ATTATTTGGGTATCA[A/G]ACCTCCTAGATTGAT | 7468 |
rs539937157 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961880 | CTTAGTGCCTGAGTG[A/G]TCTTTGAAAGGAAGG | 7468 |
rs539943205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907092 | AGCCTGCCAGGGTCT[A/G]GTTAGCTGGCTGATC | 7468 |
rs539975660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968733 | AGTACATAGTAACAA[C/T]AAGGAAAGGCTCCCA | 7468 |
rs539989121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914813 | ATTCTATTTCTTGTT[C/G]CATTAACTTGGAGGC | 7468 |
rs539998133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921300 | CCGTCTCTACCAAAA[C/T]TATAAAAAATAAGCT | 7468 |
rs540026232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876848 | TAAATTTGTTATGCC[G/T]TTTGCTGGTGCGGTG | 7468 |
rs540070253 | snp | A/G/T | 3.35685e-05 | 0.00409674 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961013 | ACGCTTTTTGTCATG[A/G/T]CCACATGCTTGTGAT | 7468 |
rs540082533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968463 | TAACCTTAGACTTTG[G/T]TAAAGTATACATGTG | 7468 |
rs540087984 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875965 | TCAAGCTTGTAATCC[C/T]AGCACTTTGGGAGGC | 7468 |
rs540094512 | snp | C/G | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982364 | GTGCCACCTTGGGAA[C/G]TATAACAACAAATAC | 7468 |
rs540100160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882966 | CAGGAGGCTGTTGGC[A/G]TCAGTCTTGGTGAAA | 7468 |
rs540114423 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883544 | GGCTGAGGCACGAGA[A/C]TTGCTTGAACCAGAA | 7468 |
rs540144085 | snp | A/G | 3.3753e-05 | 0.00410796 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974779 | AACACAACTTGTTCA[A/G]TGTGCTTTATGATGG | 7468 |
rs540150690 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886229 | TTTTTCTTTTTGAGA[C/T]AGGATCTCACTGTGT | 7468 |
rs540233362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900188 | TGTTAGTGTTGATTT[G/T]GCTTTTATGCTATTC | 7468 |
rs540274873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1954959 | CCAGGCTGAGACACG[C/T]GGCATTTTAGATGTA | 7468 |
rs540278885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961626 | ACCTAGGTGCTAGAG[A/G]GATCAATGTTCTGAG | 7468 |
rs540289652 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917850 | GCAGTGGCGTGGTCT[C/T]GGGTTACTGCATCCG | 7468 |
rs540346040 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875509 | GGTCATGAACTCCTG[C/G]GCTCAGGTGATCCTC | 7468 |
rs540379722 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941457 | GCGGGGTCGAGGCCT[C/G]CCCATGAGTCAGGGG | 7468 |
rs540381208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920773 | GTGTGGCAGCTCACA[C/T]CTGTCATCCCAGCAC | 7468 |
rs540441787 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907617 | ACCTGTTGAATCTCT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs540442040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926410 | CGCCTGCCTCAGCCT[C/T]CCAAAGTGCTGCGAT | 7468 |
rs540472845 | snp | A/G | 0.000248059 | 0.0111341 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959750 | AGAAAGGTATGTGTC[A/G]TTATCCCCTCCCCTG | 7468 |
rs540485331 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967361 | GAGGCCGGCAGATCA[C/G]AAGGTCAGGAGTTCG | 7468 |
rs540490290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919769 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAAAA | 7468 |
rs540499950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974335 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGATTA | 7468 |
rs540504263 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892319 | ATGGTGACTGTTGTT[G/T]TCCATAGCCTTCCCC | 7468 |
rs540509938 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891491 | GAATTATCAGAGTGG[C/G]CTTTAGCTGACATCT | 7468 |
rs540518963 | snp | C/T | 0.00010035 | 0.0070827 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952099 | TACCCGCCTGCTCTG[C/T]CCCCGCAGCTGTGTG | 7468 |
rs540571121 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874883 | ATGAATGGTTATTTA[C/T]AGCGAGTACTTTGGG | 7468 |
rs540581389 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982337 | TTTGACCTGACCCGC[G/T]GGGGAGAGGCAGTGC | 7468 |
rs540618237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978348 | CCCTGCCTGTCCACG[C/T]CGCGCTGGGGGACAC | 7468 |
rs540627269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938609 | GGGCTGAGAGTGTGA[A/T]AGGGGAAGGCTGGGG | 7468 |
rs540657662 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979667 | TCTCACCTGGGCCTA[G/T]CTTCTGAACTCGCTA | 7468 |
rs540672481 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912460 | TTTCTTGTAAAACCT[C/T]TTGTTTCCCTTGGAA | 7468 |
rs540695391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945765 | TGACATCAGTCACTG[C/T]GTCTGGGCCTGAGAC | 7468 |
rs540714826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906481 | CTGGGCCCCAGTGAT[C/T]CGCTTGCCTCGGCCT | 7468 |
rs540743669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942005 | CACTGACACACACCC[A/T]TTGGGTCACACCCCC | 7468 |
rs540808684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952969 | GCCCAGAATGATAAG[G/T]GACTGCTCCACCACT | 7468 |
rs540809820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949753 | TGGGCGACAGAGCAA[C/G]ACTCTGTCTCGAGAA | 7468 |
rs540849110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912403 | ATTTTGACTATGTAA[A/G]TATCATTCAGTGAAA | 7468 |
rs540859268 | snp | A/C | | | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953509 | TCCAACCCTTCAAAC[A/C]CAAGGCCGTCAAAAG | 7468 |
rs540871147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956942 | GAGTGCATGGTGGGC[A/C]TTCAGAGATCTCATA | 7468 |
rs540880349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873831 | CTGAAGTTCATAATC[C/T]AAACGTATTTTGTCC | 7468 |
rs540897362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946413 | GCTGGGACTACAAGC[A/G]GCTGCCACCACACCT | 7468 |
rs540915252 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912706 | TAACCCTCCTTCCTT[A/C]CTACTTAGATTTTCT | 7468 |
rs540929753 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870130 | ACAGGGGCCCAGCAC[C/T]TGTGAAGGGACAGCA | 7468 |
rs540934192 | in-del | -/TCTT | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1948844 | GCTTTGTGTTTTCTG[-/TCTT]TCTCTCCATGCATTT | 7468 |
rs540953607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919255 | TGGTCATGTCCTTAA[C/T]GTGTGACTCCAGGTT | 7468 |
rs541025574 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922449 | TGTATTTATATATAG[A/G]AAGATTCAAGCTTCT | 7468 |
rs541033522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943132 | CATTGTCTTAATGTC[A/G]GGGAGCAGCCTGGTG | 7468 |
rs541048653 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928478 | TTAGAACTCGTAACC[A/T]TCATACCATACAGTT | 7468 |
rs541099387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970516 | AGCTGCCGGGGGTGA[A/G]TGTGCCAGAAGGAGT | 7468 |
rs541118852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903927 | TTTTAGTAGAGACAG[A/G]GTTTCATTGTGTTAG | 7468 |
rs541131200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903527 | CTGCTGAGAACTGAT[C/T]GTCAGACATGACTGG | 7468 |
rs541138171 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932614 | AGCCAGGCGTGGTGG[A/C]ACATGCCTGTAATCC | 7468 |
rs541159248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933943 | CAAACATGGAGGAAG[A/C]CCTTAATTTGCATAT | 7468 |
rs541161049 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927720 | AGACTCTTATCTCAG[A/G]AAAAAAAAAAAAAAA | 7468 |
rs541266839 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879044 | TATTTCCTTCCAGAA[A/G]GAAGCTCTGATCTCA | 7468 |
rs541268801 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870610 | CCCTGAAGCCCGGCT[C/T]TACCGCAGCGGCGCT | 7468 |
rs541272408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939988 | CACTTTTTATACACA[A/C]GCACACAGTGTCTGT | 7468 |
rs541279194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963549 | AAGAAATGCCAAGTG[C/G]ATACTGCAGTTTGCT | 7468 |
rs541288273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878517 | TTCCTGGCTGCATTG[C/G]GTCATCTGTGAAGGC | 7468 |
rs541298366 | snp | A/C | 6.18538e-05 | 0.00556085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917089 | AATTTAATTTTTATT[A/C]TTTAAGTTAACTTAT | 7468 |
rs541311397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894232 | AAAGTGGTGGGATTA[C/T]AGGTGTGAGCCACCA | 7468 |
rs541312878 | in-del | -/TTGAA | 0.00279162 | 0.0372561 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869822 | GGCCTTGGCTCCATT[-/TTGAA]TTAATTTTTGTTAAG | 7468 |
rs541337818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948199 | TCGGAGCTCAGTGCC[A/G]CAGCATGGCTGTGGT | 7468 |
rs541359218 | in-del | -/CCTC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896664 | AACCACTGTGCCCGG[-/CCTC]CCTCCCTCCCTCCCT | 7468 |
rs541360252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923038 | GCTGCAGGCCAGTTG[C/T]GTGGGAGGTCTGCAC | 7468 |
rs541369897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908090 | CCAGCAGGCCCCTAC[C/T]TGTCTTTTTCTGTAC | 7468 |
rs541513299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891033 | CGCGTAGCTAAGACC[A/C]CAGGCACATGCCACC | 7468 |
rs541513669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949167 | GCTTGTTAAATTGGA[C/G]GTTTGAACTCAGAGC | 7468 |
rs541534926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883866 | TGGAGCTGCACGCAG[A/G]AGCTGCGTTGCTGCC | 7468 |
rs541555421 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981020 | GCAGGTAAGGGACTA[C/G]CAATGCTTACGTCAA | 7468 |
rs541593980 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980675 | CACTGGCTGGTGGCT[C/G]TCCCTTCTCCCATCA | 7468 |
rs541604933 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870014 | TTCATGGATCTATTT[C/G]TGTATTTTTCCACCA | 7468 |
rs541647938 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962749 | AGTCATAGTTCACTG[C/G]AGCCTCGATCTCCTG | 7468 |
rs541666118 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884629 | GATCTCCTGACCTCA[C/G]GATCTGCCTGCCTTG | 7468 |
rs541714722 | snp | A/C | 0.000148359 | 0.00861149 | missense | WHSC1 | GRCh38.p7 | 4:1900985 | AAAGGGATTGGGACA[A/C]CCCCTAACACTACCC | 7468 |
rs541715800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877313 | TACACACTGCCTTGT[C/G]TTTCTAAAATACAGA | 7468 |
rs541763036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969646 | CAGGAGGCCAAGGCG[C/T]GCAGTAAGCCAAGGT | 7468 |
rs541784128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903447 | TGGAGCCGAGACTTG[C/T]TCCTAGTCCTCCTGG | 7468 |
rs541849442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949695 | CTTGAACCCAGGAGG[C/T]GGAGTTTGCAGTGAG | 7468 |
rs541861747 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980714 | AGCAAAGTTAACTAC[A/G]CAGAGGACCCAGGGG | 7468 |
rs541887060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940879 | GGCTCATAGAGCTCT[A/G]CGGCTTGCCACTCTG | 7468 |
rs541889792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939929 | TCTTGGCTAACTCAG[A/T]TTCATGAAATGGACA | 7468 |
rs541895641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975883 | TTAACAGATCTCATT[A/G]ACAATGACCCTATTT | 7468 |
rs541929751 | in-del | -/GCCTGCCGTCAGCGTGGC | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951755 | GGAAGTGTGAATACT[-/GCCTGCCGTCAGCGTGGC]GCCTGCCGTCAGCGT | 7468 |
rs541934408 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980607 | AAGCGTGGGGTTCAG[G/T]GGTGTGTGGCCCTGC | 7468 |
rs541994972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908916 | GCCTCCCAAATTGTT[G/T]GGATTACAAGTGTGA | 7468 |
rs542005392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916224 | TCCGTATACTGCCTC[C/T]TTCACTGCCTCTCTC | 7468 |
rs542023236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922374 | GCGGAATCAATATTA[C/T]GAAATATGCATGTAA | 7468 |
rs542049981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877859 | CACCTTCTCTGACCA[A/C]TGATTTAAAGTACTC | 7468 |
rs542057441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947087 | GAAGCAGGTGTATTG[C/T]GGGCAGTTTTGTCAT | 7468 |
rs542069941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946567 | AGCCACTGCACCTGG[C/T]GGGGTCTTGCTTATT | 7468 |
rs542072206 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951876 | ATCCTGTTACTTCCT[G/T]TGCCATTGCTGAGGA | 7468 |
rs542107270 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882536 | GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 7468 |
rs542108257 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1954863 | GTGCTCCTGGCATCT[A/G]GTGAGTAGAGGCCAG | 7468 |
rs542135197 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877656 | AGGCTCTTGTCTTTT[C/T]CATCGTCACCCACTC | 7468 |
rs542165419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914882 | AGGGTGTGCCCTGCT[A/G]TGGATGTTGCAGTGG | 7468 |
rs542174797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921870 | TAGCCAATATTAGGC[C/T]GGGCGCGGTGGCTCA | 7468 |
rs542247014 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873976 | TCAAGTGATTCTCCC[A/G]CCTCAGCCTCCTGAG | 7468 |
rs542278030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924531 | TCAGATGGTCCTTCT[A/G]GTGCTAAGAAATGTG | 7468 |
rs542278580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890560 | CCCACCTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 7468 |
rs542281511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936971 | GATCAAGTGTTCAGC[A/G]GTAAGCTAGGTCAGA | 7468 |
rs542285903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975226 | TTTGTTGACCTAATA[C/T]ACGCCCCTTAGCTTT | 7468 |
rs542286908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908593 | AGGAAGTGAGCAGAA[A/C]AAAGAGAAGTGAGGG | 7468 |
rs542311475 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939858 | CAGTGTGAGTAATGC[G/T]CAGACTTCATAAGCG | 7468 |
rs542322666 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979833 | TACTGATGCGGCCCT[C/G]AGCTCCATGGCGAAA | 7468 |
rs542338287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889818 | AGCCGACCTTTTTTT[A/T]TTTTAATTGAGATAA | 7468 |
rs542344308 | snp | A/C/G | 9.88572e-05 | 0.00702993 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974840 | TGCTAACACTTGACC[A/C/G]AATATATCACTTGAC | 7468 |
rs542348212 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905669 | GCTGAGGACGAAGAG[A/G]ACTCTGCCGAGTCCT | 7468 |
rs542408300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936124 | AGCCCCGGGTCCTTG[C/T]GCTCCTCGCTTACTG | 7468 |
rs542520280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893193 | CTCTCAGGCCAGGCT[C/T]GGTGGCTTAAATGCC | 7468 |
rs542525138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953743 | TAAAGATGCTTAACT[A/G]TAGGAGAGGGGCAAC | 7468 |
rs542527801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943303 | TTATCTTTAATGAAC[A/G]TTTCTGACTAATATT | 7468 |
rs542557672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906602 | TTCCTGTAGTCTGCA[A/G]CAGCTTCTCTGACAT | 7468 |
rs542559216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911328 | TGCAGTGGCTCATGC[C/G]TATAATCCCAGCACT | 7468 |
rs542560408 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968997 | AAACTGTGGGACAAA[A/C]AGACCCATCCACTGA | 7468 |
rs542599839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904019 | GACTACAGGCGTGAG[C/T]CACCGCACCTGGCCT | 7468 |
rs542601216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925000 | CCCTGGTTCCTGATG[G/T]AAGGCCCATGGGGCC | 7468 |
rs542633180 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917717 | GCTGGGATTACAGGT[C/G]GGAACCACCACGCTG | 7468 |
rs542638297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872969 | CATAAAGCAAACAAG[A/T]TCTGTGAGCACAGCC | 7468 |
rs542642408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950613 | GGACTGCACGGTCAC[C/T]TGATGAGGCTGACAC | 7468 |
rs542648116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973140 | GTGAGCCACCGCGCC[C/T]GGCCGACATATTGTT | 7468 |
rs542663335 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939426 | GAGCCACGCTGGCCC[C/G]AGGTTGATGTTTTTG | 7468 |
rs542677665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886663 | GGTGGAACCCCGTCT[C/T]TACTAAAATACACAC | 7468 |
rs542680829 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917249 | TTGCTCATTTGATGA[-/CT]CTCAGAGATAACTTG | 7468 |
rs542693217 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882870 | GAGTGGGGCCCAACA[A/G]TCTGTGTTCTAATGT | 7468 |
rs542720732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910386 | ATGTGTCACCACACC[C/T]GACTAATTTTGTATT | 7468 |
rs542757361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892653 | TCGGCTCATTGTAAC[C/G]TCCGCCTCGGGTTTG | 7468 |
rs542775564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878887 | AGAGGCAGCATTGCC[C/T]GGACTGGGCCATAGC | 7468 |
rs542776809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898515 | TAAAAATACAAAAAA[G/T]TAGCCGGGCGTGGTG | 7468 |
rs542799285 | snp | C/G | | | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975120 | GTGGGTGCTGATGTG[C/G]AGTCTCTTTTGGTTT | 7468 |
rs542815968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943840 | GAAAGGCTTTTGGTG[A/G]AAATGAAGGGATTTC | 7468 |
rs542845762 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885117 | CTCTGTTTCAAAAAA[A/T]AAAAATAAAAATAAA | 7468 |
rs542859056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929251 | AGGCTATAAGAAGCC[A/G]TCTGTGGTGACTGTC | 7468 |
rs542871359 | snp | G/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870623 | CTCTACCGCAGCGGC[G/T]CTGGGGTAGCGCCCC | 7468 |
rs542882552 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970753 | CAGGCTGATTTCAGT[A/G]TGCACAAGCAGGGAC | 7468 |
rs542887823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971291 | CTACCACTTTCAGTG[A/G]CACAGAAGAAGGCTT | 7468 |
rs542889522 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904433 | TGCACTTAATCTTTC[A/T]CATCTCCAGGCTTCT | 7468 |
rs542928753 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976962 | GCTGCAGAATTGGGG[A/C]CCTCATCCATGCTGT | 7468 |
rs542955496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896134 | TTCTAGTCCAGACAG[C/T]AGCTCCACACTTGGT | 7468 |
rs543029267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958149 | CTGTCACCAGCCAGG[A/G]TCTGTGGTGCCTGGC | 7468 |
rs543064957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879470 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAATGC | 7468 |
rs543096595 | in-del | -/GAGAGAGAGAGAGAGC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872622 | AGAGAGAGAGAGAGA[-/GAGAGAGAGAGAGAGC]GCGCAGACCCTGTGA | 7468 |
rs543102806 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870854 | GCGGCGGTTTCCCCA[C/T]CCGTCCCCGCACTGC | 7468 |
rs543112932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935581 | AATAACCTCTTTGGC[C/T]GGGTGTGGTGGCTTA | 7468 |
rs543150672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977541 | AGTACTTTGGGAGGC[C/T]AAGGTGAGCAGATCA | 7468 |
rs543160765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889524 | TTTTTTTTTTGAGTC[A/G]GAGTTTTGCTGTTGT | 7468 |
rs543165556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963875 | AAATTAGCCGTGCCT[A/G]TGATTCCAGCTACTC | 7468 |
rs543197079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929763 | GTGTGTCAGCCCTGT[G/T]CCCTGCTCTCGAGAT | 7468 |
rs543243032 | in-del | -/GTGTGTG | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879826 | GGGCCCATGGCACTT[-/GTGTGTG]TGTGTGTGTGTGTGT | 7468 |
rs543244127 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977347 | GTCGTGAGATGACTC[C/T]GGCGGTGCGCAGACA | 7468 |
rs543269153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949824 | GCAAACACTTCTGTG[G/T]TAGTTTTTAATTTGT | 7468 |
rs543300911 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946062 | TCAATAGATTCATCA[A/C]CTTAGTTTTTTAAAA | 7468 |
rs543308653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934754 | TCAGGAGGCTGAGGC[A/G]GGAGGATGGCTTGAA | 7468 |
rs543370149 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957041 | TTATGTGTTTGCTGC[A/G]ACTGTCGGCAAAGTC | 7468 |
rs543508454 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960738 | CACCGTGTAAAGTGG[A/G]TTATGTAGAAGCTTG | 7468 |
rs543526935 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967211 | AGAAACACAAACTAC[C/G]AAGACTAAATCATGA | 7468 |
rs543532481 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898474 | TCGAGACCATCCTGG[C/G]TAACACGGTGAAACC | 7468 |
rs543534541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891914 | ACGAAAAACCTCACC[A/G]GAAATGCACACTAGG | 7468 |
rs543535769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922520 | ATAATTCTAATAAAA[C/T]TTCCAACAGGAATTT | 7468 |
rs543569381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903977 | CTGAACTCGTGATCC[A/G]CCCACGTTGGCCTCC | 7468 |
rs543657308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934115 | TTTTAGACAGAGTTT[C/T]GTTCTTGTTGCCCAG | 7468 |
rs543674605 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898390 | GGTTTCGTGGCCAGG[G/T]GCGGTGGCTCACGCC | 7468 |
rs543677241 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978275 | AGAAAGATGAATACC[C/G]AAGTTGAAAATCAGT | 7468 |
rs543690509 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906089 | CATTTGTTTGTGTGG[C/G]ACACAAGCAGCTCTT | 7468 |
rs543705980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872176 | AGCCGGGCCGCGGTC[C/T]GGCCCTTGGCAGGTG | 7468 |
rs543708422 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896206 | CCTTCGGGCTCTGTG[C/G]AGGCAGCCCAGTCAG | 7468 |
rs543723183 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934563 | ACATTAAATTATAAT[C/T]ATAAGGCCAGGCGCG | 7468 |
rs543757429 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981132 | ATTTTTAATCGCTTT[C/G]ATAATACTTCCAAAT | 7468 |
rs543765516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914223 | AGATGGGGTTTTGCT[A/G]TGTCGGCCAGGCTGG | 7468 |
rs543788640 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971302 | AGTGACACAGAAGAA[A/G]GCTTTTTTGACACCA | 7468 |
rs543817276 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870731 | CTCGTTCACGCCCTG[C/T]GGCCGTTAGGCGGGA | 7468 |
rs543826404 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931790 | TATAATTTAGAATAG[A/C]AAGGATATTTAGGAC | 7468 |
rs543854447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885068 | TGAGCCGAGATCATG[A/C]CATTGTATTCCAGCC | 7468 |
rs543922560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929044 | GCCAGACCCAGAACT[A/G]CAGAAGGTGTCCTCA | 7468 |
rs543924325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971236 | TGCCAAGGTGAAGTC[A/G]AAGAAAGGAGTTGTT | 7468 |
rs543930029 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919984 | TTTTCCATGAATCTT[C/T]AACCAGCATGTATTT | 7468 |
rs543936553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970713 | GATGAGAGCTGGGCT[C/G]TAGGGGCGGTTGAGG | 7468 |
rs543954151 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962439 | TCATAGGTATGGAAA[-/G]TGTTGTGGCTGCGCA | 7468 |
rs543956681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976874 | TCTAGATCTCTGCAT[C/T]GAGCAGAGAAGATAT | 7468 |
rs543957340 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981630 | GAGAACCCAGCTGTC[A/C]GTCCTCAGGCCGGCC | 7468 |
rs543985926 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934700 | TAAAAATATAAAAAT[C/T]AGCTGGGCGTGGTGG | 7468 |
rs543993534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976332 | GTCTGGGGAGCACGA[A/G]GAGGACACTCCTCTC | 7468 |
rs544021371 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979646 | CCTGGCCGGGTTGGG[C/T]CTACTTCTCACCTGG | 7468 |
rs544091833 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1893896 | AAAATTCTGGACACT[G/T]GTGGTGGCACGAGGT | 7468 |
rs544093044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940816 | ACTCATTAGAGGAGT[A/G]TAGGCCTTCCAGTGC | 7468 |
rs544109642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893362 | GTAGTCTCAGCTACT[C/T]GGGAGGCTAAGGCAG | 7468 |
rs544172611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898938 | TCAACAGTTGGTTCC[A/G]TCCATTTTCTCTCTG | 7468 |
rs544267850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875440 | GCATGTGCCACCATG[C/T]CTGGCTAATTTTTGT | 7468 |
rs544288317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923395 | AATTCTGTAAAGAGC[C/T]GAAACAATTCTGAAG | 7468 |
rs544303362 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915661 | CTTAGAGCTGCCTGC[A/G]ACCATGGGTGGGGAG | 7468 |
rs544312601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881786 | GATCTAGGTGCATAT[A/G]ATAGGGAGGTTATAC | 7468 |
rs544313110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968038 | GAGCATCTGTACTTG[C/G]AAACCAAATTGGCAG | 7468 |
rs544325227 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967500 | GGAGAATCGCTTGAA[C/G]CTGGGAGGCAGAGGT | 7468 |
rs544383232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973782 | CCAGTGTTTATCCCT[A/G]TTCACACACGTGGTT | 7468 |
rs544384744 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925659 | CCGCCTTGGCCTCCC[A/G]AAGTCCTGGGATTAC | 7468 |
rs544397336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931717 | TTTCTAGATCTCTTC[A/G]TCAGCTATCTCATTA | 7468 |
rs544403667 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966447 | GGATCACCAGGTCAG[A/G]AGATCGAGATCATCC | 7468 |
rs544441421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911460 | GGGTGTGGTCCCAGG[C/T]GCCTGTAATCCCAGC | 7468 |
rs544481334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937658 | TCCCAAGTGCATTCT[C/G]CTGTCGCCTTGTCCA | 7468 |
rs544488065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973107 | TCCTTGGCCTCCCAA[A/G]GTACTGGGATTATAG | 7468 |
rs544493861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965550 | AGATGATCAAACTTT[C/T]GAAAACCAGAAAAAG | 7468 |
rs544506004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972440 | AAGGAAAGATCTGCA[A/G]GTCTAGCCAGTGCTT | 7468 |
rs544520823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880975 | TAGTGGGTTTGTTAT[A/G]TTTAGTAATTCCTCC | 7468 |
rs544522058 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935813 | TTGCTGTGAGCTGAG[A/T]TCATGCCACTGCACT | 7468 |
rs544646078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951974 | AGACGTTTGCCCATG[C/G]ATGTTATTATATATC | 7468 |
rs544678772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905086 | AGTGAGCCGAGATCG[C/T]GCCATTGCACTCTAG | 7468 |
rs544688435 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892349 | CCTGCTTCTGAGAGT[G/T]GAGTCCCTCCCCTCA | 7468 |
rs544719188 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941873 | TGTGATGTTTCCAAT[A/G]CTGAATGCCTGTTAG | 7468 |
rs544741098 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925050 | TCTGGCTGGGTGGTT[C/T]TGAAGAATTTTCTGT | 7468 |
rs544778569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919018 | GTGGCACATGCCTGT[A/G]GTCCCAGCTGCTTGG | 7468 |
rs544804402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931082 | AGGACACAAGAAGGA[A/T]GGGGAGGGAAGGTCG | 7468 |
rs544817640 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959803 | TGGGTAATTAGGCCT[A/G]GGTTTGCTTGTGGTG | 7468 |
rs544834119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924936 | TGTCAAAGCAAAAAC[C/T]ACAAAAAATTGAGCT | 7468 |
rs544842635 | snp | A/G | 1.66388e-05 | 0.00288429 | missense | WHSC1 | GRCh38.p7 | 4:1918469 | GTCACCCCGACATAG[A/G]GAAGAGTACTCCTCA | 7468 |
rs544907871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886100 | AACTAAAGCGCGTCC[A/G]TTGAAGACGTATGCT | 7468 |
rs544917790 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971197 | GACCCTGTCTCAATT[-/A]AAAAAAAATTGTGGC | 7468 |
rs544969747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904455 | CAGGCTTCTTTCTTA[C/T]TCTTTCTAAATAGCC | 7468 |
rs545003405 | in-del | -/AATTACAGGTGC | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917572 | CTCCCAAGTAGCTGG[-/AATTACAGGTGC]CTGCCACCACGCCTG | 7468 |
rs545017887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967438 | CAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCGCC | 7468 |
rs545040997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911948 | ATGGTTTAATTTTAT[A/G]TTGTGTGTGCTGTTA | 7468 |
rs545059583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944046 | AATAACCAGGGGCAC[A/G]TGGGGGAACGTGGAT | 7468 |
rs545073900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881323 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 7468 |
rs545074665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895895 | TTGCTGAGGGCCCAG[C/T]CCTGGGCTGGCTGGT | 7468 |
rs545101147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886766 | TCGCTTGAACCTGGG[A/G]AGGTGGAGGTTGCAG | 7468 |
rs545142069 | in-del | -/CT | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913599 | AATGTAAGCTGTCCC[-/CT]CTCTCTCTCTCTGCC | 7468 |
rs545215334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893306 | AACCCCGTCTCTACT[A/G]AAAGTACAAAAAAAT | 7468 |
rs545236255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879527 | CCTGGCCTACACACA[A/T]TTTTTAAAAAATGTG | 7468 |
rs545262269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944751 | AGCCTTTATATATCT[A/G]CTTCTAAAATTGCCC | 7468 |
rs545267202 | snp | C/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960858 | GGCAACCTTTACATA[C/G/T]AGATATGTCTGAGAT | 7468 |
rs545302897 | snp | A/G | 0.00159936 | 0.0282333 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964632 | AAAGAGGTGCGCTGC[A/G]CTGCCGTTGTTATCA | 7468 |
rs545357348 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901916 | ATGGAAAGGTGTGGT[C/G]GTGCTGCTCCATTCT | 7468 |
rs545446928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873060 | ACTGCCAAATGGAGA[A/T]GAAGAGGACTCATGC | 7468 |
rs545463479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911391 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACGTG | 7468 |
rs545466140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951262 | CTGGGGCCCCGGTAC[A/G]CAGAGCGAATTTGTA | 7468 |
rs545571939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877188 | CTGTGCATGTTAGCA[A/C]TGTTCTTACATTTTG | 7468 |
rs545590094 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952656 | TCTTTATGAAGACAC[A/G]GTGTCACCTTGAGCC | 7468 |
rs545596271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961684 | AAAGTGGGCATGGAT[A/G]AAAGACAGTACATCT | 7468 |
rs545615873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972419 | GCAATTTCAAAGTCC[A/G]TGTAGAAGGAAAGAT | 7468 |
rs545676363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975839 | GTCCTGTTGACTTAG[C/T]GCCTGCCCTGCTACC | 7468 |
rs545678592 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885042 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 7468 |
rs545713332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975139 | CTCTTTTGGTTTGAA[A/T]ATCTCTTTTACCAAG | 7468 |
rs545735321 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886683 | AAAATACACACACCC[-/A]AAAAATTAGCCAGGC | 7468 |
rs545752438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929921 | TTATTACCAGGTGGA[C/G]CGAAGTCCCCAGGAT | 7468 |
rs545761196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940076 | TGAAGAATGTTGTGT[G/T]CTGTGTAGCCCTCAC | 7468 |
rs545837218 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979711 | ATTTGGGGGATAACT[C/T]TGTATATTTTTTTCA | 7468 |
rs545848528 | in-del | -/T/TTT | 0.0095749 | 0.0686504 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906655 | TCTCTCTCTCTCTCT[-/T/TTT]TTTTTTTTTTTTTTT | 7468 |
rs545856376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948246 | GGGAAAGTTCTTGAC[A/G]GAGTCTGTGTCCGCT | 7468 |
rs545857056 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949496 | GGCTGGGTGCGGTGG[C/T]TCATGCCTGTAATCC | 7468 |
rs545864755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947017 | AAGAAATGACTGAGG[G/T]AGGGGTGGGGGTCCT | 7468 |
rs545876154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932760 | CTCCATCTCAAAAAA[A/C]ATGAAAATCCATACA | 7468 |
rs545886663 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939201 | CAGTTAAACAGACTT[A/T]AAAAAAAAAAAAAGA | 7468 |
rs545889320 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979252 | AATGTTTTAATCTCC[C/T]CTGAAATGTGTAGCG | 7468 |
rs545908823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895702 | TCAGTGGCTCTCCCG[A/G]GGAGAGGGGGGCTCC | 7468 |
rs545934970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915090 | TTCCAAGCTTTCTTG[C/T]TGAATTTTTTCTTTT | 7468 |
rs545982797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921830 | ACCATTTTTCACCAT[A/T]TAATAAACGTTGTAC | 7468 |
rs546007937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961233 | GAACTGGACTTTGCC[C/T]TGTGGCAGCGCCAGC | 7468 |
rs546029060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953626 | GATTGTCACCAAAGA[A/G]CATTAATTATCTTGA | 7468 |
rs546044407 | snp | A/C | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921348 | CCTGTACTTCCGGCT[A/C]TGTGGGAGGCTGAGG | 7468 |
rs546044475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927616 | CCCAGCTACTCAGGA[A/G]GCTAAGGTGGGAGAA | 7468 |
rs546071228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968747 | ACAAGGAAAGGCTCC[C/T]ACAGGCCTTAATGTT | 7468 |
rs546155611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927129 | CTGGCAGGAGGCCTC[A/G]GTCCTTCACCATGTG | 7468 |
rs546156995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914118 | ACCTCTGCCACTTGG[A/G]TTCAAGTGATTCTCG | 7468 |
rs546204430 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889005 | CGGGTTCAAGTGATT[C/T]TTCTGCCTCAGCCTC | 7468 |
rs546244234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900391 | TGTCTTGACTGACTT[G/T]CATGTTCTTCCTTTA | 7468 |
rs546244481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938659 | CAGGGGAGGAATCCA[C/T]AATTAAGCTAGGAGT | 7468 |
rs546312898 | snp | A/C | 1.65583e-05 | 0.00287731 | missense | WHSC1 | GRCh38.p7 | 4:1900727 | AAGATGAAGCAGGCA[A/C]CAGAAATCCTCGGCA | 7468 |
rs546323765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946639 | AACGAAATTGGTTTT[C/G]ATCCCTTTGGGTACC | 7468 |
rs546331136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914278 | TCTACCCGCCTTGGC[C/T]TCCTAAAGTGCTGAG | 7468 |
rs546341778 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878165 | TCCTGGGTTCAAGCG[A/G]TTCTCCTGCCTCAGC | 7468 |
rs546402757 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955564 | TGCTCTCGTGCTGAT[A/G]TACAGATCGCTGTTT | 7468 |
rs546404759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912741 | TTGTAAAAAAGTTGT[C/T]TTCTCTCATCTTTTC | 7468 |
rs546477469 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906095 | TTTGTGTGGCACACA[A/G]GCAGCTCTTACTGAT | 7468 |
rs546490260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881869 | GCAGAGAGCAGAACG[A/G]GGATTGGGTGTTGGC | 7468 |
rs546497721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920089 | ATTCTAATAAATCTA[C/G]TGGACATGATTTTTT | 7468 |
rs546514037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875057 | ACCTGGCACTCCTGG[C/G]CTCAAGCTTTCCTCC | 7468 |
rs546522074 | snp | C/T | | | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900823 | CAGCTCTCCAGTAGC[C/T]TGCAGGAGGGGGTCA | 7468 |
rs546611997 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925766 | TTTTTATATATCTAT[A/C]TATATATTTTTTTTT | 7468 |
rs546622975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938176 | ACCCACCTCGCCCTC[A/C]TGACAGATGCGAGAG | 7468 |
rs546632829 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945987 | GTAGACTTTTGTATA[C/T]AGACCAGGTGAGAGC | 7468 |
rs546674897 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954072 | CTCACTGCAACCTCT[C/G]CCTCCCAGGTTCAAG | 7468 |
rs546680783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978498 | CTGTGGTAGACAGTT[G/T]GTCTGCCCGTCCTGT | 7468 |
rs546737655 | snp | C/T | 0.000534331 | 0.0163365 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953211 | CAGGGCCAGGTGCTT[C/T]AGCAGCATGGCTGCC | 7468 |
rs546739740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960789 | AGACAAGGTCGTGTA[A/G]GAAGCAAGGGTTGGC | 7468 |
rs546763363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893547 | TTTTGTTTTTTGTTT[G/T]TTTTTTTTTTTTGTT | 7468 |
rs546797645 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952818 | ACAGCCGTGGCCCTT[-/C]CTGCCTACTCACCGG | 7468 |
rs546826450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899098 | AATTGTGCGGGTCAG[A/T]CAGAACACATTTGTA | 7468 |
rs546829576 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925207 | GGGAGTGCTGGTGCA[C/T]ACAAGGATGGTTTTT | 7468 |
rs546890974 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898435 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAAG | 7468 |
rs546901943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919501 | TTGGGTTCCCCACTT[C/G]CCACTTTTGGTTATG | 7468 |
rs546906528 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914477 | ACTACGGGCACACGC[C/T]ACCATGCCTGACTAA | 7468 |
rs546911329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959299 | TAAGAAGGCAGAGGA[A/G]AGCTCCTCTGGGATC | 7468 |
rs546928429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973368 | TGTTGGCATTGGTGG[C/T]ATGTCCCATGTGCAT | 7468 |
rs546936122 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924098 | CAAAGCAGGCCAGGC[A/G]CAAGGTGGGAGGATC | 7468 |
rs546967455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925223 | ACAAGGATGGTTTTT[A/G]TTGGCTTGTCAGTTA | 7468 |
rs546996461 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950910 | ATATTATCACAAAAA[A/C]CAGTTGATGATGGTT | 7468 |
rs547000432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873300 | GATTATAACAGTAAA[A/G]ATTTTATTTTAAGAG | 7468 |
rs547021592 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943036 | TTGATCCAAGGCCCC[A/G]GACCAAGGGGATACT | 7468 |
rs547024678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931190 | TTGCTTCTGAGAGCA[A/G]TCCTCCTGGTTTCGG | 7468 |
rs547032846 | in-del | -/GTCA | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981803 | TTAATGCAAATGACT[-/GTCA]GTCAGTTGCCAAATA | 7468 |
rs547045436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970848 | AGGACAGGACGGAGT[A/C]CCCAACAGCAGGAAA | 7468 |
rs547075931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922674 | CTTACGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 7468 |
rs547085494 | snp | C/T | 0.000336106 | 0.0129592 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930776 | GAAGACTCTGGTAAA[C/T]ATAGCATTATGCTGA | 7468 |
rs547178032 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890784 | TCTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT | 7468 |
rs547215200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944292 | TGGAAACGGCTCTTG[C/T]TTGAAAGAACTTAGG | 7468 |
rs547232058 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896999 | AACATGGTGAGACTT[C/T]GTACAAAAACACAAA | 7468 |
rs547243985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896316 | GGCAGCCTGCAGCCT[A/G]TGAGGCTCCAGACTG | 7468 |
rs547285055 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964504 | CATGTTCTTGGAGCA[C/T]CTCGCACACAGCTTG | 7468 |
rs547293824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904680 | TTCAGGATGATTTGC[A/C]GCAAGAGTGTTTTAT | 7468 |
rs547324166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940268 | GTTCTCATGCATTTC[A/G]TGGCTTTGGTCCTTT | 7468 |
rs547332778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948493 | CTTGCGGGTGGTTGC[C/T]GAGCCGAGAGCATTG | 7468 |
rs547346661 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906636 | GATATACTGCCATTT[G/T]TACTTCTCTCTCTCT | 7468 |
rs547360174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911580 | GCGACAGAGCGAGAC[A/G]CCATCTCAAAAAAAA | 7468 |
rs547425219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928715 | ACTGGGGGCTCTGGA[A/G]TCATGGTGGGTGATG | 7468 |
rs547435697 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946548 | TGCTGGGATTACAGG[C/T]GTAAGCCACTGCACC | 7468 |
rs547473282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896942 | TTGAAAGGCCAAGGC[A/G]GGTGGATCGCTTGAG | 7468 |
rs547489967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934339 | ATCCGCCCACCTCAG[C/T]CTCCCAAAGTATTGG | 7468 |
rs547556815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940961 | AACTCAGTGGTGGTC[A/G]AGACCTGTTCACGGA | 7468 |
rs547574640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876701 | CTCAAAAAACAAACC[G/T]AAACACAAAACCCCA | 7468 |
rs547581130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969080 | AGGGGGTGCAGAGAC[A/G]CGGGAGTGCGGCCTG | 7468 |
rs547596290 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932871 | GTCGAGGATGTGCTG[C/T]GTCAAGGACCTCGCC | 7468 |
rs547599369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933636 | CCTGACCTCGTGATC[C/T]ACCCACCTCGGCCTC | 7468 |
rs547608754 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921463 | ACTCCGTCTCAAATT[A/T]AAAAAAAAAAGCATT | 7468 |
rs547631468 | snp | C/T | 6.59131e-05 | 0.0057404 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975370 | GTGTGGAGCCTCCAA[C/T]TGCAGTGGATTCCTC | 7468 |
rs547636015 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872633 | GAGAGAGAGAGAGAG[A/C]GAGCGCGCAGACCCT | 7468 |
rs547659023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932536 | CAGATCACCTGAGGT[C/T]GGGAGTTTGAGACCA | 7468 |
rs547694375 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869463 | AGTGATTCTCCTGCC[C/T]CAGCCTCCTGAATAG | 7468 |
rs547698122 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937055 | GCTCTGGTCACCTAA[-/T]TTTTTTTTTTTTTTG | 7468 |
rs547722558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915739 | GACCACTTAATTGGG[A/G]GAATCTCCAGAAGAC | 7468 |
rs547758630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890760 | CCCACCACCACGCTT[A/G]GCTAATTTTCTATTT | 7468 |
rs547772626 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906926 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 7468 |
rs547772777 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947223 | AGTGGGACAAAGTTG[A/G]GTTGATAGGATATTT | 7468 |
rs547778759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895275 | CTGCTTTTAATTCTT[C/T]TGGGTAGACAGACTG | 7468 |
rs547805979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877411 | CACTGGCTTTCTGAC[C/T]CTCACTGCACTACTT | 7468 |
rs547834865 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943284 | CAGATTCTTTGGCTG[C/T]GTTTTATCTTTAATG | 7468 |
rs547839568 | in-del | -/TCTTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896839 | TCCTTTCTTCTCTTC[-/TCTTT]TCTTTTCTTTCTCCT | 7468 |
rs547862868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896247 | CTGTCCTGCACCTCC[C/G]TTCTGTATTCCGGCT | 7468 |
rs547863996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969945 | GCAAAGCCTAAACCT[C/G]AAGGAACACACTAGA | 7468 |
rs547869077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890248 | TGCTTTTTGCTATTA[C/T]GAATAATGCTGCTGT | 7468 |
rs547871724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927957 | TGCAGTGGTGCAATC[A/G]TAGGTCACTGCAGCC | 7468 |
rs547907940 | in-del | -/T | 0.157972 | 0.232445 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892573 | AACCACTGATAACTC[-/T]TTTTTTTTTTGAGAC | 7468 |
rs547921985 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883434 | GCCAGGAGTTCAAGA[A/C]CAGCCTGGCCAACAT | 7468 |
rs547939196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968392 | AGGGAGCACCGGGAG[C/T]GTGGTGACGCCAGGG | 7468 |
rs547970864 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980842 | ACTCTAACTTCTCCC[A/C]AAGTGTCCTAAGAAA | 7468 |
rs548038567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889977 | CTCTGCACTGTTAAG[C/T]AGTCACTTCCTATCC | 7468 |
rs548063398 | snp | C/T | 0.00188553 | 0.0306466 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974734 | CTGTCTCAGTGGACA[C/T]AGGACACCACGGTTT | 7468 |
rs548094046 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955546 | TGTGGTGAAAATGAC[A/G]TTTGCTCTCGTGCTG | 7468 |
rs548103140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961304 | TTTCTTCTGAGGTGC[A/G]GCGTGTCTTTCAGCT | 7468 |
rs548104599 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979934 | TAGGGCGCTGCAGGC[A/C]CCGGGGACCCCAGCA | 7468 |
rs548132801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947845 | TGAAGGGATTTGTTT[C/T]GTCAAAAAATTAAAA | 7468 |
rs548145434 | snp | A/G | 3.31192e-05 | 0.00406921 | missense | WHSC1 | GRCh38.p7 | 4:1955178 | AAAATGATGCGGTGT[A/G]TCCGCTGCCCCGTTG | 7468 |
rs548180171 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946074 | TCACCTTAGTTTTTT[A/T]AAAAAAATCTATAAA | 7468 |
rs548241207 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930118 | GTGCAAGGTTGTCTC[C/T]GTGTGCTGGCCTGGG | 7468 |
rs548257451 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955068 | TAGCATTAACTTTTC[-/A]AATTCATGGAGGCTG | 7468 |
rs548275108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968293 | TCTTAAATAAGTCAG[A/G]TTGTGTCAAATTATG | 7468 |
rs548277946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932982 | AGAGTTTGGCTGGCT[C/G]TGCCATGTGGTGCCT | 7468 |
rs548310589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902068 | ATGGGGCAGCAGTCT[C/T]TGTTCATCTGGTGGT | 7468 |
rs548386467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882641 | TGCACTCCAGCTTGG[G/T]CGACAGAGCAAGACC | 7468 |
rs548387504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939534 | AAAGTTAAGCCAGAA[C/G]GACAAAGGAATTCAG | 7468 |
rs548388873 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937963 | AATTGGAAATCCTCA[A/G]TATAGTGATACTAGT | 7468 |
rs548406849 | snp | C/T | 0.000219366 | 0.0104707 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974651 | GCGCTCACTAAGGCT[C/T]GGTCCTCTCCACGTG | 7468 |
rs548415494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938729 | AAACTGTTTTAATGT[A/G]TATGTTATTTTGAAG | 7468 |
rs548473613 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932497 | CCCGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 7468 |
rs548483418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876582 | CTATAGTCCCAGATA[C/G]TTGGGTGGCTGAAGT | 7468 |
rs548510815 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978395 | GCTCCTCTCAGTTGC[C/T]GAAACATAAAGAGAC | 7468 |
rs548536486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915194 | AGTCTCGGCTCACTG[C/G]AAGCTCCGCCTCCTG | 7468 |
rs548593573 | in-del | -/CGCTGC | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964630 | CAAAGAGGTGCGCTG[-/CGCTGC]CGCTGCCGTTGTTAT | 7468 |
rs548594993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921404 | GTGGAGGTTGCAGTG[A/G]GCCAAGATCGTGCCA | 7468 |
rs548597293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914654 | TTTTCTATCTTCACA[C/T]TTGATTGATGGTTTG | 7468 |
rs548600548 | snp | A/C | 0.000131833 | 0.00811782 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1957986 | CTTCAGAGGGAAGCC[A/C]GAGAAACACAGGAGA | 7468 |
rs548602396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965717 | ACATAACAGGGGAGG[A/C]CTCAAGAAACTTACC | 7468 |
rs548607467 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920879 | CTAAAAAAAAAAAAA[A/T]TTTTTTTAATTAGCC | 7468 |
rs548670762 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902443 | TGCCCAGGCTGGTCT[C/G]AAACCCCTGGGCTCA | 7468 |
rs548671779 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882104 | TAGATTGAGTTGGTG[C/T]TGGGGAAGGTTCCGG | 7468 |
rs548681096 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956505 | CAGATCTGAAGGAAG[C/G]GTCCTGTTGTCTCGA | 7468 |
rs548716728 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947360 | GGGCTATGTGGCTAC[A/G]GCTACACAAAAGCCT | 7468 |
rs548738983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880493 | ATCAGTTGTGTGCCA[A/G]TGATGAGCCAAGACC | 7468 |
rs548739880 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976935 | GGAGGGATTCAGGCA[C/G]CCCAAGGCCCAGCTG | 7468 |
rs548760948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930049 | GCATGCTCCGGGTGC[C/T]GATGCTGGCAGCCCT | 7468 |
rs548770036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888266 | AAAATACAAAAATTA[C/G]CCAGGCCTGGTGTTG | 7468 |
rs548773983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895217 | CTTTTGGCTACTGTA[A/C]TAGTGCTCCTGTGAA | 7468 |
rs548805744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931912 | AATGAGCCAGCTCTT[A/C]CTGAAGCCAGATTCA | 7468 |
rs548814559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879203 | TATACAACACTTTTT[A/G]AAATTATTTTATTTT | 7468 |
rs548852837 | snp | A/G | 4.39107e-05 | 0.00468545 | missense | WHSC1 | GRCh38.p7 | 4:1978901 | CGGAGAGTCACAGAG[A/G]GCAAATAGCGCCAGG | 7468 |
rs548875746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971605 | TACTTTTCAGAGGCA[C/T]ATGTACTGAGGCGTG | 7468 |
rs548881152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894248 | AGGTGTGAGCCACCA[C/T]GCCTGGTGAAGATTT | 7468 |
rs548894132 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897300 | CAGCCTGGACAATAT[A/C]GTGAGATCCATCTCT | 7468 |
rs548912421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929627 | TGGGGCTGACATCCA[A/G]TAAAACTTTGTGGGC | 7468 |
rs548921223 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895712 | TCCCGGGGAGAGGGG[C/G]GCTCCCCATGAGCAG | 7468 |
rs548954106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910890 | ATGGTCATGCTTGTC[C/G]TTTGTTTCCCAGGGA | 7468 |
rs548957730 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972902 | CTGTCGCCTAGGCTG[C/G]AGTTCAGTGGCACAA | 7468 |
rs548958365 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921876 | ATATTAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 7468 |
rs548979354 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968986 | CATCTTCACTGAAAC[C/T]GTGGGACAAACAGAC | 7468 |
rs548985120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909761 | TTCTCCTGTCTCAGC[C/T]TCCCGAGTAGCTGGG | 7468 |
rs548997159 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924988 | TGCCCTGCCCACCCC[-/T]GGTTCCTGATGTAAG | 7468 |
rs548998438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977099 | GCTGCACTACAGTGG[G/T]AATGGAGGGGCCCAG | 7468 |
rs549011505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941312 | CGGTTATTCACTTGA[A/G]TTGTTGCTTATACTG | 7468 |
rs549017392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917987 | GGTTTTGCCATGTTG[A/T]CCAGGCTGGTCTTAA | 7468 |
rs549059803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879795 | ATTTCTACCAGAACC[A/G]GGTGTTGCAGACCCT | 7468 |
rs549065533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897199 | AAAGGAAAGTGGTTT[G/T]GGCTGGGTGCAGTGT | 7468 |
rs549111465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885755 | GTTACCACCCAGAGA[C/T]CTCTGCACCGGTTCT | 7468 |
rs549116786 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977645 | GACTGGTGTGGTGGC[A/G]TGCACCTGTAATCCC | 7468 |
rs549130773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903001 | GCAACATAGCGAGAC[C/T]CGGTCTCTATAAAAA | 7468 |
rs549137730 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896892 | AAAGATAGTTAAACC[C/T]GGGTATGGTGGCTCA | 7468 |
rs549159092 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916603 | TGCCTCGGCCTCCCA[A/G]AGTGGTGGGATTACA | 7468 |
rs549169788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949490 | CACTCTGGCTGGGTG[C/T]GGTGGCTCATGCCTG | 7468 |
rs549174500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885345 | GACACCTGCTTATGG[A/G]TCAGTGGAGCATTAT | 7468 |
rs549188781 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933271 | CTTACTTGTACCTCT[C/G]CCTGAGGCCTTGCTG | 7468 |
rs549199410 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878249 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 7468 |
rs549224019 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899970 | AATACTGGGTTGAGC[A/T]TAGCCAGACCTGACT | 7468 |
rs549234767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956544 | AGCAGGCTCTTGGGG[A/G]CTCGCTTTACCTTTC | 7468 |
rs549250131 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928758 | CAGAGGTGGGTGGGA[A/G]GGCAGCAGGCCCGTG | 7468 |
rs549289388 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982547 | GTCCCCAGGCCCACA[C/G]CCAAGTAAGTCAAGG | 7468 |
rs549305018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897644 | TTTTATTTTTATTGA[C/T]ATATTTTTGAGACAG | 7468 |
rs549329830 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981902 | TGTCACAGCCTCACC[A/C]TACCCTGTTGAGGTG | 7468 |
rs549330400 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971970 | GACACTTGTGGCCGG[G/T]TCAGAAATAAGGCAG | 7468 |
rs549407116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949867 | GCTCCCTGCAATGTC[A/G]GCTAAATGTGGAAAA | 7468 |
rs549423089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884122 | CGGGGAGGAGATGGG[G/T]TCTTGCTCTGTCACC | 7468 |
rs549440592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971444 | GAAGGCAGAGATCCT[A/G]GACAGATGATGAGCA | 7468 |
rs549442985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922088 | GGAGGCAGAGGTTGC[C/T]GTGAGCTGAGATCAC | 7468 |
rs549547075 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975785 | AACCATTCTCCCTGC[A/G]AACATGACTGTTGAC | 7468 |
rs549555052 | in-del | -/AA | 0.0792508 | 0.182605 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880612 | TGAAATACTCCTGCC[-/AA]AAAAAAAAAAAAAAT | 7468 |
rs549560366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922600 | TTGGCCTGAGGATTT[A/G]CTCTACCAGATAGGA | 7468 |
rs549618779 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884938 | ACATGGAGAAACCCT[C/G]TCTCTACTAAAAATA | 7468 |
rs549620527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941119 | GAAAAGGCAAATTTT[A/T]TACAAATTATTTTTC | 7468 |
rs549631806 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869691 | TTATTTGTTTGGTGA[C/T]AGAGACGAGGTCTTG | 7468 |
rs549633695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963207 | AGATGGGAAGCAGGT[C/G]CATAAGGGCGAGAGT | 7468 |
rs549681950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891339 | TTTGCAAACTTGGGT[G/T]TTCCATTTCAGTCTT | 7468 |
rs549696810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970809 | GGGCATGCAGGCTGA[C/T]GGGTCACATAAAGGG | 7468 |
rs549748546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973447 | CCAACGTGCACATCA[G/T]CACCGCGGCTCAGCG | 7468 |
rs549752264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934474 | CTCCAGCCTGAGCTA[C/T]AAGAGCGAAACTCCA | 7468 |
rs549785289 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933744 | ACCCTGAACCCCTCC[A/G]TAAAGCAGTCATGCA | 7468 |
rs549788616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948574 | TGGTGGGAAAAAGTC[A/G]GAATCTCTGCAATCT | 7468 |
rs549792008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923772 | CAGTGTCCAAAACCA[A/G]AAAGCTACCCAGTGA | 7468 |
rs549796965 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981399 | CCAGCTTTGTTCTGA[A/G]GACGTGGTGACTTCC | 7468 |
rs549798808 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926151 | TTTTTGGGCCTGAAT[-/T]TTTTTTTTTTTTTTT | 7468 |
rs549800200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917314 | ATATATGTGTATACA[C/T]ACACACAGACAGAGG | 7468 |
rs549806174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923346 | AAAAAAAATTCTTAT[A/G]TGTCAAGGACACCAT | 7468 |
rs549810888 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896663 | TGAACCACTGTGCCC[A/G]GCCTCCCTCCCTCCC | 7468 |
rs549812106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929497 | AGAGCTGGTTGGTGC[C/T]GAGCCAGTCAGCAGA | 7468 |
rs549838738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885267 | TGCTATAAGGCATTT[C/T]AGCAAATTAGTGGAT | 7468 |
rs549874060 | in-del | -/ATT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893687 | TCCCCAGTAGCTGGG[-/ATT]ATTATGGGCATGCAC | 7468 |
rs549922148 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981787 | CTGTTTTATAATTCA[A/G]GTTAATGCAAATGAC | 7468 |
rs549962407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927819 | TTTGTAGAGTCTCCA[A/G]TTACGTTGGCAATGT | 7468 |
rs549964196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921647 | TTTTACCAGCTGTGG[C/T]GGCGAGCGCCTGTAA | 7468 |
rs549967626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897608 | AACAAGACAAGATCC[C/T]GTCTCTACAAAAAAT | 7468 |
rs550045147 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872036 | GGTGGGAGGGGCAGG[G/T]TGGGGTCCCGGGGCC | 7468 |
rs550073611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900326 | TTGGCAAGTTAAGTT[A/C]TGTGTCCATGGCCAC | 7468 |
rs550111171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909162 | TATTAAGTTCCTTTA[A/G]GTTGTATGCCTTTGA | 7468 |
rs550111700 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903002 | CAACATAGCGAGACC[C/T]GGTCTCTATAAAAAA | 7468 |
rs550146891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902973 | TGAGCCCAGGAGTTC[A/G]AGACTAGCCTGGGCA | 7468 |
rs550174525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916511 | CCACCACACCCGGCT[A/G]ATTTTTGCATTTTTC | 7468 |
rs550184219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913571 | GATCTCTCTGAGAAA[C/T]GCATAGAAGAAATAA | 7468 |
rs550198209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883539 | CAGGAGGCTGAGGCA[C/G]GAGAATTGCTTGAAC | 7468 |
rs550208755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945282 | GCTGGAGACGTTAAG[A/C]GCTGAGCACACCACA | 7468 |
rs550240596 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870203 | ACTCCTTGGTGGCTG[A/G]AGGTGGGTCCGGGGA | 7468 |
rs550294702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912536 | CAGCCTTAATTTTTT[G/T]CAAGTATTCATCTCC | 7468 |
rs550332546 | snp | C/T | 0.000169967 | 0.00921708 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953124 | AGCTGGAGCTCAGAT[C/T]GCAGCAAGGTAATCC | 7468 |
rs550355435 | snp | G/T | | | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975256 | TTGAAGAGAAAGGCA[G/T]GTGTTTCCAATTTGG | 7468 |
rs550362594 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970026 | GTGCAGCTGAAAGAA[C/T]CTGGGAAAGAGAGAA | 7468 |
rs550380324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883968 | AAGCTTGTTTAACTT[A/G]AGACAACTTATTCTT | 7468 |
rs550414966 | snp | C/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933435 | TCTGTCGCCCAGGCG[C/G]CTGGAGTGCAGTGGC | 7468 |
rs550441728 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890645 | TCACTTTCGTTGCCC[A/C]GGCTGGAGTACAATG | 7468 |
rs550472006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969130 | GGGGCCTGCCCCCAG[C/T]GGCGCTGAGAGTTGA | 7468 |
rs550484886 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980744 | GAAACGAGCTGTGTA[A/G]CCACTGACTTGCTCG | 7468 |
rs550506195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925160 | TGCTTCCATCTGTAA[C/T]CTAGGTCTTTCTACA | 7468 |
rs550531337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975509 | GGCTGGCTTGTTGCC[A/G]GGACAGGTGGGAGCA | 7468 |
rs550532382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892761 | CTTTAGTAGGGACGG[G/T]TTTCACCATGTTGGC | 7468 |
rs550551908 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899306 | CTCCACCTCAGTACT[A/G]TGGACATCTCGGGCC | 7468 |
rs550570790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905300 | GTTGCGATGTGGCGA[A/G]TGCGGAGTTAGAACT | 7468 |
rs550581767 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943591 | GCTGGACTGTATGGC[C/T]GAGGGCTGGTTGGGT | 7468 |
rs550596354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886890 | ACTTCCAGATTGATA[C/T]ATGTTCAATTCTATC | 7468 |
rs550611053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952598 | TAAGGGTACAGGTAA[C/T]CTGGTTGGTCACCGA | 7468 |
rs550674606 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959235 | GTGCACAGACACTAA[C/G]ATAAAATAATGTGAG | 7468 |
rs550710506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898389 | TGGTTTCGTGGCCAG[A/G]TGCGGTGGCTCACGC | 7468 |
rs550715148 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874047 | CCTGTCCTTTTTAGC[A/T]GGGCAAGTGGGCAAA | 7468 |
rs550734352 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950997 | GGGGTGGGGCGGGAC[A/G]AGCCTGCCTGCAGGG | 7468 |
rs550788582 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962153 | ATCCCCTACCCCTGC[-/A]GTAGTGGGGCAGCAG | 7468 |
rs550809903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951320 | TTCCCCAATCTCACC[A/G]TCACTCACTCATCTC | 7468 |
rs550824117 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982657 | CCCGTCCTGATGGCC[A/G]CCTAGGGAGGGACTG | 7468 |
rs550827208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873588 | GTAGAAGACAACCCA[C/G]TCCTCCTAATCCTGT | 7468 |
rs550842631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904581 | CTTCATCTGATTGAA[G/T]TAGTGTTAAGGGACA | 7468 |
rs550846215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880689 | GGAAATACAGGGGCA[A/C]GAGAAATACTACAGA | 7468 |
rs550863381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964670 | CTCAGTCGTTACAAG[C/T]CCCTCCCCCTCCAGC | 7468 |
rs550880115 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WHSC1 | GRCh38.p7 | 4:1871904 | GGCCATGTTGGGCCC[A/G]GCCGGGCCCTGCGGC | 7468 |
rs550893127 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928823 | GATGTGTTGTGGATC[C/T]GAAGCCCTGTGCAGA | 7468 |
rs550992300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951613 | GGCTGTGGGCTGAGG[A/G]GGCCATCACTAGACC | 7468 |
rs551037859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936364 | GTACTTTGTTTGAAT[A/T]TCTATTTTATTCGAT | 7468 |
rs551042844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912443 | ATGTTCTGTAATTGC[A/G]TTTTCTTGTAAAACC | 7468 |
rs551050019 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944224 | AGTGGGCTCATCCTA[C/G]AGGAGCGGAGTTTTC | 7468 |
rs551105696 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982174 | ATGAGTATTTTTGTA[G/T]TAAAAACATTTTAAA | 7468 |
rs551111516 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943435 | TAAAAATGATAAAAT[G/T]GCCATCATTCTATTT | 7468 |
rs551120740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959216 | GCTCTTGTTCATCAG[C/T]GATGTGCACAGACAC | 7468 |
rs551174033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923962 | TCTGCGTCCATCTAA[A/G]AAGTGTAAGTGGGCA | 7468 |
rs551182199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966748 | AAATTCTAACATTTT[A/G]TTTTCTATATAATTT | 7468 |
rs551185425 | in-del | -/T | 0.00249376 | 0.035223 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918126 | AACTTACAGTGTCTC[-/T]TTTTTTTTTCCCAGC | 7468 |
rs551206914 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954173 | TATTTTTAGTAGAGA[C/T]GGGGTTTCATCATGT | 7468 |
rs551222522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950883 | TTTTCTACATAGCCT[A/C]ATTGACGGGTTATAT | 7468 |
rs551224218 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885728 | CTTGGTACCCATGCA[C/T]TGCTCCTCTTTGTTA | 7468 |
rs551235994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930119 | TGCAAGGTTGTCTCC[A/G]TGTGCTGGCCTGGGC | 7468 |
rs551330849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917885 | CTCCCAGTTCAAGTG[A/T]TTCTCATGTCTCAGC | 7468 |
rs551357902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936205 | ACCAACCAAGGAAAC[A/G]CCGGGTTATTCTGTC | 7468 |
rs551365643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972083 | CAAACAGTGTCTCTC[A/G]GAGAATGTGACGGCT | 7468 |
rs551368674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911696 | TAATTATTGGTAAAA[C/T]AAAAACAGTGAGATA | 7468 |
rs551374309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892714 | GCTGGGATTATAGGC[A/G]TGCACCACCACGCCT | 7468 |
rs551407444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873483 | AATCAGCTTATCCAG[A/G]GCTTTCAAACCAGTA | 7468 |
rs551427631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876281 | TTTCCTAAAACCACC[C/T]GGCCCCAGATGAGTT | 7468 |
rs551434767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873958 | AGTCCCAAACTCTTG[G/T]GCTCAAGTGATTCTC | 7468 |
rs551440731 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904090 | CTAAAACACAGCAAG[G/T]GAGCACACTCCATTT | 7468 |
rs551480723 | snp | A/G | 3.39334e-05 | 0.00411892 | missense | WHSC1 | GRCh38.p7 | 4:1918577 | GAAGCAGGAAGGGAG[A/G]TGCAGCATCCCAGTT | 7468 |
rs551482168 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1954911 | GCACAATGCCCAGGT[C/T]GGCTGCCCACGTGCC | 7468 |
rs551498326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903773 | GGAGTCTCGCCCTGT[C/T]GCCCAGGCTGGAGTG | 7468 |
rs551516156 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880580 | CAGTGAGCAAAGGTC[A/C]TATCTTTGAAAAATC | 7468 |
rs551516992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918787 | CAGCCATTCTGACCC[G/T]TGAGGGAAAAGATAC | 7468 |
rs551559073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897657 | GATATATTTTTGAGA[A/C]AGAGTCTCACTCAGG | 7468 |
rs551568835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972738 | TCAGCAAACCGAAAA[C/T]GCATGAAGCAAAAGG | 7468 |
rs551586198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928620 | AGGCGTGGTGGCTGT[C/T]TTGTGAGGCGAGGTG | 7468 |
rs551625351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910491 | AACTATATGTTTTAG[A/G]TATTACACTCACTGG | 7468 |
rs551628611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880087 | TTTCATAAAAATGTG[A/G]ATTTCTAGATTTTTG | 7468 |
rs551652781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892223 | ACTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTTG | 7468 |
rs551659273 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962930 | CTCTGTCAGGGCGCA[A/C]CACCCAGGGGATAAG | 7468 |
rs551671276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878328 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 7468 |
rs551673309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885128 | AAAAAAAAAATAAAA[A/T]TAAAAAAAATAAAAT | 7468 |
rs551697700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978022 | ATCCTGGCTACTCGG[A/G]AGGGTGAGGCAGCAG | 7468 |
rs551723391 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982598 | CTACCTGTTCCCCAC[C/T]CTGTGGGCCAGGGTG | 7468 |
rs551734622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977669 | TAATCCCAGCTATTC[A/G]GGAGGCTGAGGCAGG | 7468 |
rs551737886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935691 | ATGGTAATACCCCGT[C/G]TCTACTAAAAATACA | 7468 |
rs551738597 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870390 | CGAAGGTGTTCCCGG[C/T]TCCCTGAACCTGCGT | 7468 |
rs551804902 | in-del | -/CAG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882675 | TCTCAAAAACAACAA[-/CAG]CAACAACAACAACAA | 7468 |
rs551833415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895349 | AATCAGTGTCTTGCT[C/T]ATAGTAGGCACTTTA | 7468 |
rs551833452 | snp | A/G | 0.000214445 | 0.0103526 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901062 | ATACATGAATGGGAA[A/G]CCTCTCTTTGAATCT | 7468 |
rs551868131 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879612 | TCTTTGCTGGCCAGT[C/T]CTTTGTGGTTGCTGT | 7468 |
rs551892281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900489 | CTGCCTTCTGTGACC[C/T]GAATTATTATAAAAA | 7468 |
rs551912091 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926558 | TCACTGCAACCTCCG[C/T]CTTCCGGGTTCAAGC | 7468 |
rs551921180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1950044 | AGGTGTACAGGAAAT[C/G]TAGTTTATGCTTTTG | 7468 |
rs551921535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957797 | CCACTGACAGTTGTT[C/G]ATAGACTCTAGTTTT | 7468 |
rs551924146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939489 | TACAGTTTGTCTGCT[C/T]TTGTTTATGTTCAGA | 7468 |
rs551967093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917288 | ATTTATATATACACA[C/T]ATATGTACGTATATA | 7468 |
rs551989619 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870981 | CGCGCGCCCAACGCC[A/G]GCCTCCGCGGCCGCG | 7468 |
rs552006484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875624 | TCCAGACAGATTGGC[C/T]GGGTGCAGTGGCTCA | 7468 |
rs552033558 | snp | A/T | 0.030278 | 0.119257 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957376 | GCAACCTCCACCTCC[A/T]GGGTTCAAGCAATTC | 7468 |
rs552038191 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906878 | ATTGGCCAGGCTGGT[A/C]TCAAACCTCTGACCT | 7468 |
rs552069969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875114 | CTACAGGCAGATGCC[A/G]CCATGCTTGGCTAAT | 7468 |
rs552086383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923226 | AGGCATGGTGACTCA[C/T]GCCTGTAATCCCAGT | 7468 |
rs552099705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914506 | AATTTTTTGTGTTTT[A/G]GTAGAGACAGGGCTT | 7468 |
rs552109524 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891396 | GCTTGGTCCGTCTCA[C/T]GGCCTGGCTCTGGGG | 7468 |
rs552112374 | snp | A/G | 0.000172059 | 0.00927362 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974598 | TTTGCCATCATGGAG[A/G]ATGCTGGGAGCTCCA | 7468 |
rs552191659 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968244 | GATCCAAGAAGTAAC[A/C]GTGAACAGACAAGTT | 7468 |
rs552200811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938883 | TACTGTAAATTCTGT[C/T]ACCCTTCAGTACCCT | 7468 |
rs552203713 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980786 | CCTCTGAGGGGCACT[C/G]GCCGGTTAAGACAGG | 7468 |
rs552251218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973872 | GTGCGGTGGATCTGG[C/T]GGCTCCTCAGGTGGA | 7468 |
rs552258374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947609 | CTGTGCTGTTAACTT[A/G]GAAGACCTGTTTGAA | 7468 |
rs552287394 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907733 | TTCTCCTGCCTCAGT[C/T]TCCCAAGTAGGTGGG | 7468 |
rs552288309 | snp | A/G | 7.51993e-05 | 0.00613139 | missense | WHSC1 | GRCh38.p7 | 4:1978842 | AGAAGCCCCCCCCAG[A/G]GCCAGGGAAGCCGAA | 7468 |
rs552319436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946810 | TTCCTTTGGGACATT[C/T]TTACAGCAGGGTGTC | 7468 |
rs552319492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955091 | GGAGGCTGAGTAATT[A/T]TTAGTTGCTCTTTTC | 7468 |
rs552354957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931868 | TAAATTTAGAGACGT[A/G]TTCCTTTTAAATGAC | 7468 |
rs552359332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971928 | CTAAAAGACATCAGC[A/G]GCTGCCAGCTGATGC | 7468 |
rs552381985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888174 | TCCCAGCACTTTGGG[A/G]GGCTGAGGTGGGTGG | 7468 |
rs552394718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945783 | CTGGGCCTGAGACGT[G/T]CATGGAGGGCTGTAA | 7468 |
rs552432239 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954115 | CTCATCCCTTCAGTA[C/G]CTGGGATTACAGGCA | 7468 |
rs552446858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960059 | AGATGGGGTCTTGCT[A/G]TGTTGCCCAGGCTCA | 7468 |
rs552509983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967632 | TTACTGGGACATAGC[C/T]CCATTGTAAGAGTGT | 7468 |
rs552533333 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947592 | TCCACTTTAACATTT[C/T]ACTGTGCTGTTAACT | 7468 |
rs552542648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920857 | TGGGCAACATGAAAC[A/C]CTGTCTCTAAAAAAA | 7468 |
rs552593642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920187 | GGGCGTGGTGGCTCC[C/T]GCCTGTAATCTCAGC | 7468 |
rs552597324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931500 | TGTAAAAATAACTGA[C/T]ATATTAGGGTATCAA | 7468 |
rs552604154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926442 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGTTTGGCT | 7468 |
rs552605678 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925776 | TCTATATATATATTT[A/T]TTTTTGTTTGTTTGT | 7468 |
rs552610398 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937555 | AAGTAATGGTGTCTT[A/G]TCTCTTCAGATTTGG | 7468 |
rs552670957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953012 | TCAAGGAGGAAAGGC[C/T]TCTTTTCATAGGAGC | 7468 |
rs552673550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937026 | TAGTTACCAGGAAGC[C/T]TGCACTTAACATTTG | 7468 |
rs552687077 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874370 | CTGTCCTTCCTCTTT[C/G]AGCATAATTCATGGC | 7468 |
rs552696479 | snp | C/G | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982667 | TGGCCGCCTAGGGAG[C/G]GACTGGGTCCCCGGA | 7468 |
rs552705793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893551 | GTTTTTTGTTTTTTT[G/T]TTTTTTTTGTTTTGT | 7468 |
rs552706127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905350 | TGTGATCTGATCTGT[G/T]CACCCTCTGGAAGTG | 7468 |
rs552726872 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951769 | CTGCCTGCCGTCAGC[A/G]TGGCACCTGCCATCT | 7468 |
rs552732337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943653 | ATACATAGCCCCAAA[G/T]ATGGTCTAGGAGCAA | 7468 |
rs552766651 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899542 | TCAGATTTTCCCTAG[C/T]GTCTGATGCTATTGA | 7468 |
rs552769936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893605 | ACCCCAGGCTGGAGT[G/T]CAGTGGTGCTTTCTT | 7468 |
rs552878166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911911 | ATGTAAGGAGCATTT[A/T]TCTGTGTCATTATTT | 7468 |
rs552904034 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973599 | CTGGTACCATTTCTG[A/G]TTTTAAAGGGTGGCC | 7468 |
rs552920369 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925504 | CCCGGGTTCAAGCGA[C/T]TCTCCTGCCTCAGCC | 7468 |
rs552974806 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979018 | AGCTCGAGCCGCCAG[A/G]ACACAGACGTACAGG | 7468 |
rs553013725 | snp | A/G | 5.21989e-05 | 0.00510849 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978626 | GTGCTCACATCTTGT[A/G]TTCTGTTGCAGGGAA | 7468 |
rs553071366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893181 | ATGCATATTAAACTC[G/T]CAGGCCAGGCTCGGT | 7468 |
rs553101259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924830 | TACTCAGGAAGCTGA[A/G]GCAGGAGGACCACTT | 7468 |
rs553116914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885577 | TGCATTTCTGCCTCT[A/G]GGGAGTCTCAAGTGG | 7468 |
rs553167618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944589 | GAGGTGAAAACTTGT[C/G]AGAATATATAAAAGC | 7468 |
rs553228973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951845 | AAATATCTTGGATGT[A/G]TCCTTCAGGGTTGTG | 7468 |
rs553238589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952684 | GCCTCAGTTTCAACA[A/G]AAAGAACAGCTCCAG | 7468 |
rs553279195 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876886 | CACGCCTGTAATCCC[A/G]GTGCTTTGGGAGGCC | 7468 |
rs553308048 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963363 | CCCTGTGTAGACCCC[-/T]GGGAGGGTTTTAGCC | 7468 |
rs553323463 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951553 | AAAAGGTGAGGTGCT[A/G]GGCCTGTTTTAGCTT | 7468 |
rs553336659 | snp | A/C/T | 0.0115144 | 0.0749975 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881625 | TGGTCTTGAATTCCT[A/C/T]GACTCAAGCAGTCCT | 7468 |
rs553349679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905079 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 7468 |
rs553357768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873016 | ATGTGTGCTCTCATT[C/T]CCCACAACTGATGGT | 7468 |
rs553372982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966268 | AAGTTGTATGAAGAA[A/G]AAAGATCTCAAAGTA | 7468 |
rs553381346 | snp | A/G | 2.0031e-05 | 0.00316467 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978855 | AGAGCCAGGGAAGCC[A/G]AAGGGGAAGAGGCGG | 7468 |
rs553383211 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939429 | CCACGCTGGCCCCAG[A/G]TTGATGTTTTTGGGG | 7468 |
rs553404684 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924280 | TCTGAATGGACACTC[C/T]AGTGTTTGACAGCTA | 7468 |
rs553420075 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945483 | TAAGATTATAAATTA[A/G]CATCTAGTTCCAAAA | 7468 |
rs553444416 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961009 | CAGCACGCTTTTTGT[A/C]ATGGCCACATGCTTG | 7468 |
rs553483159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976159 | GAGCTGTTCTGCCTG[C/T]GGTGGCCTCCTTTGC | 7468 |
rs553483686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965399 | ACCACCAAGCAGACC[A/G]ATATATCTATTGTGG | 7468 |
rs553488310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915493 | TTTCATAGCACACAG[A/G]GTTTCTCTGTTGGGT | 7468 |
rs553521905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975766 | GCTTGTAGCAGCACC[A/G]CCCAACCATTCTCCC | 7468 |
rs553541178 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933939 | TGAGCAAACATGGAG[C/G]AAGCCCTTAATTTGC | 7468 |
rs553558818 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980475 | AAGTTTACAGAACTC[A/C]CCTTGAAAACTGCTG | 7468 |
rs553565734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961634 | GCTAGAGGGATCAAT[A/G]TTCTGAGGAAAAGGA | 7468 |
rs553575245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973208 | CTGTAAGTCAGTTAA[A/G]ATAAATAAAACAGGG | 7468 |
rs553575849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877143 | TTCTGTCTCAAGGAA[A/G]AAAAAAAAATTGTTA | 7468 |
rs553627885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969576 | GCTGGGCACAGTGGC[A/G]TGTGCCTGTTGTCCC | 7468 |
rs553652068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935840 | CACTCCAGCCTGGGC[A/G]ACACAGCAAGATTCT | 7468 |
rs553653507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943009 | AGTATTATTGTGAAC[A/C]ATTTAACCCTTTTGA | 7468 |
rs553666213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935392 | CCTTCCAGGCTGGTA[G/T]TCAGCAGAAGGCTTG | 7468 |
rs553681856 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959275 | TGTTGCCCTGCCTGC[C/T]TCTTGTGCTAAGAAG | 7468 |
rs553694668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962564 | TCCATAAATAGAAAA[A/T]GCAAATGTGGTAAAA | 7468 |
rs553698175 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979657 | TGGGCCTACTTCTCA[A/C]CTGGGCCTATCTTCT | 7468 |
rs553717048 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916098 | GGGTTACTCTGTGGT[C/T]TGAGCTGCTCTCTGA | 7468 |
rs553741302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922220 | GTCTATGTAGAAAAC[G/T]CAAGAGAATGTACAG | 7468 |
rs553770581 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955424 | TCATTCCTTGTCTGC[A/G]CTGTGTTCATTGATG | 7468 |
rs553810917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970212 | AGAATCCTGTAGATA[A/C]CCAGGCAAAAAAACA | 7468 |
rs553814182 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887192 | TGGGCTTCATTCTTC[A/C]CAGTGTGGTCTATCC | 7468 |
rs553819969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895625 | TCCATACTGTCCCAT[A/G]CCTGGCTCCTGGAGG | 7468 |
rs553851592 | snp | A/G | 1.7416e-05 | 0.00295088 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953533 | TCAAAAGGTACAGGT[A/G]CACCTGCGCAGCCTT | 7468 |
rs553853615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960943 | ATGTGTGTGGTGCCC[A/G]TTCTAAGTGATCATG | 7468 |
rs553877181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928052 | TTGCCACCATACCCA[A/G]CTAATTTAAAAATAA | 7468 |
rs553894482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890331 | TGAGATGGCGTCTCG[C/T]TCTGTCGCCTAGGCT | 7468 |
rs553974502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874602 | TTTGTAAGTAATGGA[A/G]CATCTGGGAGAAGAA | 7468 |
rs553995498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927586 | TAGCCAGGTGTGGTG[A/G]TGCATGCCTATAATC | 7468 |
rs554015039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895974 | TGGTGATGAGGAAGT[C/T]CTCTGCCTGGTGGTG | 7468 |
rs554016509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925841 | GGGTCTTACTCTGTC[A/G]CCCAGGCTGGAGTGC | 7468 |
rs554029324 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1892243 | CTCCTGCCTTGGTCT[C/T]CCAAAGTGCTGGGAT | 7468 |
rs554048449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926886 | CTTGGTATTAGTTAT[C/G]TATTGTTGCATAACA | 7468 |
rs554136839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914924 | CTGTTTTAGTTGGAG[A/T]CTTGATTTTGGGTTT | 7468 |
rs554150567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901409 | GCTTTGGGTTGGAGG[C/G]TGGGCTCCAGGATGC | 7468 |
rs554150609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967858 | GGGGTCTGGCATCTC[A/C]TTGTAACCATGTGTG | 7468 |
rs554196113 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904521 | TAGTGATTGATTCAA[A/G]TGTGATGTGTTGCCA | 7468 |
rs554201689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973992 | AGTTCTAGGCCACAT[C/T]GTGCTTGCATTTGTG | 7468 |
rs554239605 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939241 | TTGGACATTTGAACG[C/G]TAGCTGATGATATAA | 7468 |
rs554254196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875840 | CGTTAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 7468 |
rs554259253 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872893 | AAATGTTTTAAGTGC[C/T]CTAGTTACGTATTTA | 7468 |
rs554268608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914704 | GTTGAGAAGAATTCC[C/T]CTAGGAATTTTGAAG | 7468 |
rs554292536 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889491 | TGAGGCACCACGCCC[A/G]GCCAAGATTTGACTT | 7468 |
rs554334461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906502 | GCCTCGGCCTCCCAA[A/C]GTGCTGGGATTACAG | 7468 |
rs554336982 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926767 | TGAGCCATTGCACCA[A/G]CCTGAGTTTTTAATT | 7468 |
rs554355310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883088 | TGTGTTGTTTGGGAT[A/G]AGGAGAGATGAGGGG | 7468 |
rs554363926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894784 | AGGTAGAGGATTTTT[A/G]GGGGTATACGTAACA | 7468 |
rs554409531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919770 | AACCCCGTCTCTACT[A/T]AAAATACAAAAAAAA | 7468 |
rs554434713 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979541 | GTGTTGTAAGATTTC[C/T]TCCCGTAGTTTTTTC | 7468 |
rs554436167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874556 | AAACAGCCCATTTTA[A/G]TGCCGATATCTGGCC | 7468 |
rs554492041 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979474 | TTGTTCCTCAGAAAC[A/G]CTTCTTTTCCATCCT | 7468 |
rs554508094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888460 | TATGCCAGAGAATCA[C/T]CTGTGCATATCCTCA | 7468 |
rs554523903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883565 | TGAACCAGAAGGTGG[A/T]GGTTGCAGTGAGCCC | 7468 |
rs554540555 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976407 | TGGAGTGTAGCTCGC[C/T]CTTCTGCCCTATTTG | 7468 |
rs554544191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921696 | TTGAGAAAGGAGAAT[C/T]GGTTGAACCTGGGAG | 7468 |
rs554556789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927484 | GCACTTTGGGAGGCC[A/G]TGGCGGGCAGATCAC | 7468 |
rs554575731 | snp | C/G | 0.000165802 | 0.00910348 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961139 | CCACTTCTACATGCT[C/G]ACTATAGACAAGGTA | 7468 |
rs554577379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969358 | GGGACCCAGCCAGTA[C/T]CCGCTCCAAGAAATC | 7468 |
rs554602332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900162 | GGAGGGATTGGGATG[A/G]GCTCTTTTCCTGTTA | 7468 |
rs554604140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961212 | GAGCCCTGATGGTCA[C/T]CTGTAGAACTGGACT | 7468 |
rs554640364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975715 | CCAGGCCTGTCTCCC[A/G]TTCCTGGTGGCGGCC | 7468 |
rs554641724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960227 | TGAAAGGTATCTGCT[A/G]TAACTCACACATTCC | 7468 |
rs554654211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967756 | TCATGTGGGTGACAT[C/T]AGACGAGACCAGCCT | 7468 |
rs554678803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903666 | TTATATAGAGATCTT[C/T]AAAATGTTGAACACC | 7468 |
rs554688437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968683 | ATGTAAGTGGTTTAA[A/G]TGTATAAGTTAAGAC | 7468 |
rs554715473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967316 | CGGGCACGGTGGCTC[A/G]TGCCTGTAATCCCAG | 7468 |
rs554719615 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934288 | TGGGGTTCCTCCATG[C/T]TGGTCAGGCTGGTCT | 7468 |
rs554740005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890324 | TTTTTTTTGAGATGG[C/T]GTCTCGCTCTGTCGC | 7468 |
rs554754969 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979115 | GATGACCGTCTGAGC[C/T]CAGCTCAGCGTTCCT | 7468 |
rs554758242 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901376 | GCCTGGTACTTCCAG[C/T]CACTTGCCTGAGCCC | 7468 |
rs554769028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900555 | CAAAGCTGTAGAGGT[C/T]CTGGCATACCTATCC | 7468 |
rs554793547 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932195 | TAATCCCAGCACTTT[G/T]GGAGGCCAAGGTGGG | 7468 |
rs554803250 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931335 | GTCCTTCCTAGGCCT[A/T]CGGCTTAAAAAAACC | 7468 |
rs554833822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973452 | GTGCACATCAGCACC[A/G]CGGCTCAGCGCGTCA | 7468 |
rs554835085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881515 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 7468 |
rs554908433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925345 | GACTTCAGGACTTTT[C/T]GTTGCTACTTGCTGA | 7468 |
rs554918999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931338 | CTTCCTAGGCCTTCG[A/G]CTTAAAAAAACCAAA | 7468 |
rs554926647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946210 | AATACTCACAAAGCT[A/G]TTATTGGCTTCTTAA | 7468 |
rs554947288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887329 | TGACATGTTCTTCTT[C/T]TTTTTTAAATCTCCC | 7468 |
rs554956401 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905602 | AGCAGGTGGCTGCTA[G/T]GAATGGGGTACAGAG | 7468 |
rs555038122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957489 | AATGGGGTTTCAGCA[A/T]GTTGGCCAGGCTGGT | 7468 |
rs555051427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964145 | ATTTAAAGGAGAATG[C/T]GAACTAAGTGTATTA | 7468 |
rs555053114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956889 | AGCTTGGTTAGCTCC[A/G]TGCTGCCAGAAGCTT | 7468 |
rs555068998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920232 | AGGTGGGCAGATCAC[C/G]TGAGGTTAGGAGTTT | 7468 |
rs555079488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886120 | AGACGTATGCTTTGT[C/G]AGTCTTGTAATCAAA | 7468 |
rs555112421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963521 | GTCTAAATGTAAACT[A/G]CTTATGTGCTGTAAG | 7468 |
rs555166174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949696 | TTGAACCCAGGAGGC[A/G]GAGTTTGCAGTGAGC | 7468 |
rs555168290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872054 | GGGTCCCGGGGCCGG[C/T]GCCGGGGCCAGGGGT | 7468 |
rs555213655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924953 | CAAAAAATTGAGCTC[C/T]GTGTTAATGTCCAAC | 7468 |
rs555323581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934576 | ATTATAAGGCCAGGC[A/G]CGGTGGCTCACGCCT | 7468 |
rs555373266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950328 | CGAGCAATTCCACTC[A/G]CTCAGGGATTCCATG | 7468 |
rs555374240 | in-del | -/AAAAAAAAAAA | 0.46014 | 0.13543 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965052 | TGTCCAGTGTTCAGC[-/AAAAAAAAAAA]AAAAAAAAAAAAAGC | 7468 |
rs555379849 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923216 | AATCTAGGCCAGGCA[G/T]GGTGACTCACGCCTG | 7468 |
rs555386977 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933747 | CTGAACCCCTCCGTA[A/C]AGCAGTCATGCAAAT | 7468 |
rs555391900 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887742 | AGCTAAATCATACAC[-/TG]TGATGGATAATATTT | 7468 |
rs555416803 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926187 | TTAAGACGTAGTCTC[A/G/T]CACTGTTGCCAGGCT | 7468 |
rs555452636 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870478 | CATGGGCGGCGGGCA[A/G]CAAATCACACCGGCT | 7468 |
rs555475632 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950750 | GTTCCAAAAAGCCTG[-/T]CTTAGTTCACCTACT | 7468 |
rs555530381 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909317 | CCTAGGTTCTTTGAG[G/T]ACAGAATAGTATGTA | 7468 |
rs555530683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917411 | GAATTCTAAAATTGG[C/T]TTTTAAAAGTTTTTA | 7468 |
rs555538786 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959294 | TGTGCTAAGAAGGCA[A/G]AGGAGAGCTCCTCTG | 7468 |
rs555546233 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922897 | TGCCATTGTACTCCA[G/T]CCTGGGTGACAGAAC | 7468 |
rs555556938 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940464 | ACCTAAATTTTTTGC[C/T]GTTGCCAAAAACAAC | 7468 |
rs555592048 | snp | A/G/T | 5.18402e-05 | 0.00509096 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917056 | ATAGATGACCCTTCA[A/G/T]TCTACTTTTAGACCA | 7468 |
rs555617924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971166 | GAGTTCGAGACCAGC[C/T]TGGGCAACATAGGGA | 7468 |
rs555635722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901760 | AGTGTCCACTTACTG[C/T]CTCCTCAGCCAGGTG | 7468 |
rs555657558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928901 | GGAGTGAGTGGGCTC[A/G]TGGAGTGAGTCATGG | 7468 |
rs555715101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948146 | GAGAAAGTATTTTCA[A/G]ACTGAAGAAAACTTT | 7468 |
rs555720583 | in-del | -/TGA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887006 | AATATTGTGGTGGTT[-/TGA]TGATCTATTCCAGAA | 7468 |
rs555746708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884316 | GCCCAGGCTGGTCTC[A/G]AACTGCTGAGCTCAA | 7468 |
rs555746781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891364 | AGTCTTTTCCGCCCC[C/T]GGAGGAATGGGTTGG | 7468 |
rs555753497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896449 | TCACAGCTCACTGCA[G/T]TGTCAACCTCCTGAG | 7468 |
rs555758872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890882 | GATTACAGGGGTAAG[C/T]CACCACGCCCGGCCT | 7468 |
rs555772499 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870431 | CCAAGGCCGCCGGCT[C/G]CGGCAGCACCTGGAG | 7468 |
rs555848297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877814 | TTACCCCTCACCCTC[C/G]TTCAGGTCTTTGTGC | 7468 |
rs555914045 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970327 | GTGGGCTCCTCAGAA[C/T]GAGCCAGGGGTGTCT | 7468 |
rs555930045 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981593 | GGTCACCTGTGGGGG[A/G]AACTCTTCAGGCACC | 7468 |
rs555947293 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970013 | GGGAGTGAGCAGAGT[A/G]CAGCTGAAAGAACCT | 7468 |
rs555996555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962679 | CCTAGGTTTTGTTGT[C/T]ATTTTTCTTTTTTGA | 7468 |
rs556028322 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976208 | GATCCTGGAGCTGTG[G/T]GTCTGCTGAGATGCT | 7468 |
rs556035962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876998 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGTGCCT | 7468 |
rs556089431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956839 | GGGTCAGTGCTGGCT[C/T]CTGTGTGACTGCAGG | 7468 |
rs556122349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909270 | TCCCACCACCCCCCC[C/G]AACCCTAGCATCAGC | 7468 |
rs556137701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927629 | GAGGCTAAGGTGGGA[A/G]AATCGCTTGAACCCA | 7468 |
rs556168415 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883708 | CCATCTGCTCTCCCA[C/G]CTGTAGTGGAAGCCC | 7468 |
rs556168796 | snp | C/T | 0.000148595 | 0.00861831 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939797 | AAATAATAATAATAA[C/T]GATAACCATGGCATT | 7468 |
rs556190104 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895627 | CATACTGTCCCATGC[A/C]TGGCTCCTGGAGGAT | 7468 |
rs556203003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933229 | GAGGTGAGGCTCTGT[A/G]AATGCATTGGCAGCA | 7468 |
rs556204462 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | WHSC1 | GRCh38.p7 | 4:1916919 | AGTTCTTTGGTGACG[C/T]CCCAGAAAGAGCTTG | 7468 |
rs556229822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890524 | GCCAGGATGGTCTCG[A/G]TCTCCTGACCTCGTG | 7468 |
rs556294614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884249 | TATGGGTGCATGCTA[C/T]TGTGCCTGGCTAATT | 7468 |
rs556378538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933689 | GTGAGCCACCGCGCC[C/T]GGCCCTGCAAGATGT | 7468 |
rs556404484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921081 | AAGGTTAGTAAACCA[A/G]GAATAAAAGGGAACT | 7468 |
rs556447027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954555 | CGAGGTCTCACTGTT[C/G]TGTTGCCCAAGCTGG | 7468 |
rs556447618 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980964 | CCTTAGAGTCGAAGG[A/C]CCCAGGGCCCCGCTG | 7468 |
rs556547384 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958922 | GCTGATTTTCAGCTG[C/T]CTCTACTGCTTTGTT | 7468 |
rs556555650 | snp | A/G | 1.6729e-05 | 0.00289209 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961018 | TTTTGTCATGGCCAC[A/G]TGCTTGTGATTTCCA | 7468 |
rs556585044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936815 | ACATATTGCTAAGGT[C/G]TAAATATGTGGACAC | 7468 |
rs556597572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944476 | TACATGGAACCATTT[A/T]AGTCCCATTTGACTC | 7468 |
rs556619800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901718 | GAGCTGTGCAGAGGT[A/G]CTCCCGCTGTCCTTA | 7468 |
rs556706105 | snp | C/T | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952338 | AGGACAAGCCCCCTC[C/T]CCACCCCCACCGCCT | 7468 |
rs556715480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915356 | CCTGACCTCGTGGTC[C/T]GCCTGCCTCGGCCTC | 7468 |
rs556727115 | in-del | -/AG | 0.00159617 | 0.0282053 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982089 | GGGATATACTGAAAT[-/AG]AGAGTTGAGACTTGC | 7468 |
rs556737584 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919704 | TTTGGGAAGCTGAGG[C/T]GGGTGGATCATGAGG | 7468 |
rs556737910 | in-del | -/TGCGC | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964624 | GTGCAGACAAAGAGG[-/TGCGC]TGCGCTGCCGTTGTT | 7468 |
rs556802206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951701 | CCATCTGTCAGCTGG[A/C]GATGGCATGGGAGCT | 7468 |
rs556819893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882998 | AGCTTGGTGGTTGGC[C/G]ATTCTTGGGATTGTG | 7468 |
rs556842377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936053 | TCATGTTATTGTTTA[A/C]TGAATGGGAATACTA | 7468 |
rs556874032 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911784 | ATAGTAGAAAATTCG[G/T]TTATGTTATCCGGTT | 7468 |
rs556887898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876031 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 7468 |
rs556899358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930908 | TTGGGCCAGCGGTCC[A/C]AGTGCGTGTGGTCAC | 7468 |
rs556959082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893081 | TGATTCCTCTAAGTC[C/T]GCATCCCCAGGTTTG | 7468 |
rs556990411 | in-del | -/ATGCGTGTATTGA | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972204 | CCACAAAGAGCATTG[-/ATGCGTGTATTGA]ATGGAGCAGGCTTCT | 7468 |
rs557077029 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891863 | CTCCATCTCAAAAAA[A/C]AAAAAAAACAAAAAA | 7468 |
rs557083880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900141 | CCTGATACCTCAGCT[A/G]TAACAGGAGGGATTG | 7468 |
rs557089232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891455 | AGGGTTGAGACCTCC[C/T]TCTGCTCAGTTGGAT | 7468 |
rs557120551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930288 | TGGCACTGGCTCTAC[A/G]GCTAATTTTTCAGGG | 7468 |
rs557219224 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958124 | ACCCAGGCTATGGCT[C/G]GGGAGAGGACTGTCA | 7468 |
rs557274163 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981641 | TGTCCGTCCTCAGGC[C/T]GGCCTTTCTTCCGGC | 7468 |
rs557296384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903835 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 7468 |
rs557304310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965036 | ATTATTAGACTTAAC[A/G]TGTCCAGTGTTCAGC | 7468 |
rs557365637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972236 | AGCAGGCTTCTGTGG[A/G]AAGTTCGGCAGTGTC | 7468 |
rs557382262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929757 | GCATTAGTGTGTCAG[C/T]CCTGTGCCCTGCTCT | 7468 |
rs557389981 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908868 | CACTCCAGGCTCAAA[-/CTC]CTGGGCTCAGGTCAT | 7468 |
rs557395285 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888029 | GATGGACCATCTGTT[A/T]TTTGCATCTCATGTC | 7468 |
rs557409325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885524 | CTGTCTCAGTGGCCC[C/G]TGTTGACATGTATTT | 7468 |
rs557424841 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950940 | TCCACTGTGAAATCA[A/C]TGGCGGTACAGGACC | 7468 |
rs557426522 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910806 | TTTCTACTTGTAGTT[C/G]TGGCAGTTTCTGCTT | 7468 |
rs557431201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950510 | ACGGTCAGCCTGTGG[C/T]GTGAGTCCGGAAGAC | 7468 |
rs557475571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971706 | GCCAGCCGGTGGGGT[A/G]CACCTGAAAAGCATG | 7468 |
rs557563025 | in-del | -/CTGCC | 0.00398882 | 0.0444803 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964632 | AAGAGGTGCGCTGCG[-/CTGCC]CTGCCGTTGTTATCA | 7468 |
rs557579242 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883453 | CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 7468 |
rs557584126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872640 | AGAGAGAGAGAGCGC[A/G]CAGACCCTGTGAAGA | 7468 |
rs557594067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923468 | GATGCTGCTCAACTG[C/T]GGCCATGCCCAGGAA | 7468 |
rs557594488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911129 | GCCCAGAGAGTCACA[A/G]ACTACCTGTAGTCTA | 7468 |
rs557616162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942742 | GTTAGAGTTGCTTCT[C/T]CTCTAGTTTGTAACT | 7468 |
rs557635265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964948 | ACAATCAAAACAAGA[A/G]CAATAAATAAAAATA | 7468 |
rs557660677 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881179 | CCCTCCCGGACTCAA[A/G]TGGTCCTCCCACCTC | 7468 |
rs557672481 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903215 | GCAGTGGAACAATTT[A/C]CTCATGTGTATAGTG | 7468 |
rs557675457 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905965 | GACCTTCAAGCCTCT[G/T]CAGCCCGGGTGCAGG | 7468 |
rs557677490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941820 | AACAAATAAACTTGT[C/G]TATTATATATTAACG | 7468 |
rs557706516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923052 | GCGTGGGAGGTCTGC[A/C]CTGGACGTGGTGCTG | 7468 |
rs557706558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929710 | TTCAGACATTGAACA[C/G]AAACAGGTGGTGGGT | 7468 |
rs557738681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898449 | GCGGGCGGATCACGA[A/G]GTCAGGAGATCGAGA | 7468 |
rs557760216 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943726 | TAAAATTAAAATTCT[A/C]AAAAAAAAACCCCAC | 7468 |
rs557801913 | snp | C/T | 3.29554e-05 | 0.00405914 | missense | WHSC1 | GRCh38.p7 | 4:1904264 | GGAAGAGACAAAGAC[C/T]ACCTGTTGAAATACA | 7468 |
rs557804064 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959017 | CTGCCTAGCACTGCT[C/T]CTCCTGGGGTGGACT | 7468 |
rs557880288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903166 | GTTTTGGGCCGGCCT[C/T]TTCAGCTTACAGGTG | 7468 |
rs557924869 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892088 | TTTTGTTTGTTGCTC[A/T]ATTTCCAAGTGCTGG | 7468 |
rs557929251 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911602 | CAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAAAAA | 7468 |
rs557945828 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909266 | TTTTTCCCACCACCC[C/T]CCCCAACCCTAGCAT | 7468 |
rs557985560 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922489 | AATTCTCCCTTTAAT[A/C]ATCTATAAATTCAGT | 7468 |
rs558009798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964463 | GGCACAGCAGCGGCT[A/C]CCCATGCCCCACAGA | 7468 |
rs558020329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896662 | GTGAACCACTGTGCC[C/T]GGCCTCCCTCCCTCC | 7468 |
rs558054535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908726 | GTCCCCATTGTCACT[A/G]ATGAGGGACCTGTGG | 7468 |
rs558073585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971637 | GGTCCGAGCCAGGGC[A/G]TGGACCTGTATGTGA | 7468 |
rs558076157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879286 | TGCAGTGGAGTGATC[G/T]CAGCTCGCTGCAAGC | 7468 |
rs558107706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920422 | CACTCCAGCCTGGGT[A/G]ATCCTTAGGGCTTTT | 7468 |
rs558152010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885034 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 7468 |
rs558170729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926026 | CAATCTGGACTCAAA[C/T]TCCTGGCCTTAAGCG | 7468 |
rs558185955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934631 | GAGGCAGGCGGATCA[C/T]GAGGACAGGAGTTCG | 7468 |
rs558188380 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951281 | AGCGAATTTGTAGTG[G/T]CTTTTCCCTTCCCAC | 7468 |
rs558194669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976853 | TTTGTTCCACCAGCC[A/G]CACATTCTAGATCTC | 7468 |
rs558205463 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875906 | GCGAGACTCCATCTC[-/A]AAAAAAAAAGAATTC | 7468 |
rs558215585 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883824 | AGGAGCTGCCTAGAT[A/G]GCGATAAGAAGCGAG | 7468 |
rs558291397 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899960 | CTGAGATAAGAATAC[G/T]GGGTTGAGCATAGCC | 7468 |
rs558311949 | snp | C/T | | | downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1982211 | TTTCTTAACTTATTT[C/T]ATATGGGATTGTTTG | 7468 |
rs558327214 | in-del | -/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940612 | CGTGATGCTGTTTTT[-/C]CTCATTGTAGACATG | 7468 |
rs558336758 | snp | A/G | 0.000212789 | 0.0103126 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978919 | AAATAGCGCCAGGCG[A/G]CCGCTTGGCCGGATC | 7468 |
rs558387374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938375 | CTTTTGTTGTTCTTT[C/T]TCTTTTTTTTTCCTT | 7468 |
rs558413845 | in-del | -/A | 0.214843 | 0.247516 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883632 | CAAGACTTTGTTTCC[-/A]AAAAAAAAAAAAAAA | 7468 |
rs558418848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949547 | GCGGGTGGATCACGA[C/G]GTCAGGAGTTCAAGA | 7468 |
rs558441606 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869805 | CACAGGTGTGAGCCA[C/T]TGGCCTTGGCTCCAT | 7468 |
rs558457973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905402 | ACTAGGCCAATGCTC[C/T]AGTCCAATATTGCTG | 7468 |
rs558478709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967950 | GTCTGGTGTCTTATT[G/T]TCAAGATGGGTTATC | 7468 |
rs558482202 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949037 | TGGGTGACTCTCTGA[C/G]TGGGGCCCCAGACAG | 7468 |
rs558555945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882447 | AGGCGGGTGGACACG[A/C]GGTCAGAAGATCGAG | 7468 |
rs558558556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874228 | GATAAGCATTTTAGT[C/T]TTCTGAGCCTCAGTC | 7468 |
rs558561464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932574 | CAGCATGGAGAAACC[C/T]CATCTCTACTAAAAA | 7468 |
rs558618855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898050 | GGTGGAACTCCAGAC[A/C]CTTTAATATTGTTCC | 7468 |
rs558647865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962399 | AATTTTAATTTGGAC[A/C]GGAGGCTGTTCTTCA | 7468 |
rs558678075 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893782 | ACTTCTGAGCTCAAG[C/T]GATCTACCTGCCTCG | 7468 |
rs558721650 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904815 | TAAATTGATTTTTAC[A/G]TGGAGCGGCTGATGT | 7468 |
rs558738170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978305 | TCCCTTGGGAGAGGG[C/T]AGGTCACATGGAAAT | 7468 |
rs558783286 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907884 | CCAATGGGATTACAG[A/G]CATGAGTCACTGTGC | 7468 |
rs558850941 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886549 | TTAAAAAGTAACTTG[C/G/T]GGCTGGGCGCGGTGA | 7468 |
rs558872541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977873 | GCTCATGCCTCTAAT[C/G]CCAGCACTTCTGAGA | 7468 |
rs558879756 | snp | A/G | 2.21929e-05 | 0.00333106 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953238 | TGCCTCTGAAGAGGA[A/G]TTGCTTGATTTTAGT | 7468 |
rs558880771 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933553 | CGCCACCATGACCAG[C/T]TAATTTTTTTTTTTG | 7468 |
rs558887251 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979866 | AGTGACTTTGCAGGG[C/T]GTGAGACCGCAGTCT | 7468 |
rs558887444 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943208 | ACTTGCCCTTCAGCT[C/T]ATAAAAGCAGAAGGT | 7468 |
rs558915806 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875255 | TGAACCACTGTGCCC[A/G]GCCAAGTTGCAGTAT | 7468 |
rs558942784 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939239 | AATTGGACATTTGAA[C/T]GCTAGCTGATGATAT | 7468 |
rs558965585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893019 | TAAACGAGGAATTCT[G/T]AGGTTATTAGTCTTC | 7468 |
rs558985823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931006 | CCTGTGGCTCCCTTG[C/T]TCTCCTACCCAAGTT | 7468 |
rs558999958 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944361 | TGCTGCTAATTTAAC[C/G]TGGAATTCCTTCATT | 7468 |
rs559047720 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966387 | TAGGGCTGGGCATGG[C/T]GGCTCACGCCTGTAA | 7468 |
rs559057826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925260 | GGCCAACCCTTGAGG[C/G]ATAGAGTCAGGTGGA | 7468 |
rs559062410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919256 | GGTCATGTCCTTAAC[A/G]TGTGACTCCAGGTTA | 7468 |
rs559137356 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907965 | GTTACCCCCAAATAC[A/G/T]TCAGAACAAGGACAG | 7468 |
rs559158432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936131 | GGTCCTTGTGCTCCT[C/T]GCTTACTGCCAGCAT | 7468 |
rs559173206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924885 | TGAGCCATCATTGCG[C/T]CACTGCACTCCAGTT | 7468 |
rs559234046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892664 | TAACCTCCGCCTCGG[A/G]TTTGAGCGATTCTCC | 7468 |
rs559235298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930886 | CCCTGTTTCTGACCC[A/G]TGGGGTTTGGGCCAG | 7468 |
rs559247486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930424 | TTCACTGGCACTATT[C/G]TAATTTATGAGTTTT | 7468 |
rs559249019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904435 | CACTTAATCTTTCTC[A/G]TCTCCAGGCTTCTTT | 7468 |
rs559259051 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879290 | GTGGAGTGATCTCAG[C/G]TCGCTGCAAGCTCCG | 7468 |
rs559266523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873372 | TTTATCGTATCTATT[C/T]GTATGTAACATATAA | 7468 |
rs559296819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898520 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 7468 |
rs559317445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965741 | ACTTACCATCACGGT[A/G]AAGGTGAAGGGTACC | 7468 |
rs559361503 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924559 | GTGCTAAAAATGAAA[G/T]TCTGGATTGGCACTA | 7468 |
rs559386543 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909815 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGCTG | 7468 |
rs559426609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972634 | CCCTCACACCACTTA[C/T]AAAGGCCAATTCCAG | 7468 |
rs559464018 | snp | A/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902196 | GTTTAGTTCTCGCTC[A/G/T]TGTAATGGCAGTGGT | 7468 |
rs559466917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886712 | GCGTGGTGGCGTGCA[C/T]CTGTAGTCCCAGCTA | 7468 |
rs559468565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880535 | TCCCATGGGTTTTAT[A/G]GGCCTGTAATGGGAT | 7468 |
rs559475329 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912995 | AATAAGAATAGTTAT[A/G]TTAGACATAGAATAT | 7468 |
rs559506897 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870242 | CTGGGCTGAGGTGTC[A/G]TTCTATAGCCCGGGT | 7468 |
rs559528286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886127 | TGCTTTGTGAGTCTT[A/G]TAATCAAAGGTGACA | 7468 |
rs559550289 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885078 | TCATGCCATTGTATT[-/C]CAGCCTAGGTGACAA | 7468 |
rs559571111 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977999 | GGTCGTGGTGGCGGG[C/T]GCCTGTAATCCTGGC | 7468 |
rs559581791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872317 | TTGAAGCCTCAGTGC[A/G]TGAGATGGGACCTGG | 7468 |
rs559645771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971826 | CAGAGTCATTTTCAT[C/G]AACACCAGAAAATCA | 7468 |
rs559646291 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982572 | TCAAGGGAGTACCCC[A/G]AGGGCTGATCCTACC | 7468 |
rs559652520 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899424 | CCTAGTGGTGGTAAT[-/A]AAAAAATGCTTCCAG | 7468 |
rs559658673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884625 | TCTCGATCTCCTGAC[C/T]TCACGATCTGCCTGC | 7468 |
rs559665497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950627 | CCTGATGAGGCTGAC[A/G]CTTACTTCATCTGTG | 7468 |
rs559750288 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956275 | AAAATTTGATCTTTA[C/T]AGAAAATACTGGACT | 7468 |
rs559798830 | snp | A/C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870898 | GGACGCCGCTAGCAG[A/C/T]CTCCCGCGGGCCCCA | 7468 |
rs559862816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947419 | CAGTGGTGCTCTGGG[A/T]GTGGAGACTTCCTCT | 7468 |
rs559864327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957675 | CATAGTGGAGGACAG[G/T]GAGCTCCCGACAGAA | 7468 |
rs559914403 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971351 | AGATGCACCCTAAAT[G/T]TAGGGCCTTCCCACT | 7468 |
rs559928021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957220 | TCGGTTCTTGCTTGA[A/G]CCTATGGTTAATCTC | 7468 |
rs559944912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923193 | AAAACTATGTATGTT[A/G]AAATGAAAATCTAGG | 7468 |
rs559945800 | in-del | -/GTGGGGCTTACACCTTTCAAAGAAGTCA | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962223 | TGTCAATCACAGGTC[-/GTGGGGCTTACACCTTTCAAAGAAGTCA]GTGTCATGAAGGACA | 7468 |
rs560039850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976983 | TCCATGCTGTGGGGG[C/T]GGGGCGGCCAGGAAG | 7468 |
rs560050651 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929259 | AGAAGCCGTCTGTGG[G/T]GACTGTCTTGGGAGG | 7468 |
rs560055571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875575 | TTTTAAAGAATTGAT[A/T]GATTTGATTACATTT | 7468 |
rs560056564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881885 | GGATTGGGTGTTGGC[C/T]CCATGAGGGTGGGGG | 7468 |
rs560060311 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888857 | AGGCGTGAGCCACCA[C/T]GCCTGGCTGCTTTAT | 7468 |
rs560080782 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958252 | GGAGTGTGAGGCTTG[G/T]CTTGGTAGCTTAGAG | 7468 |
rs560096724 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970455 | AGATGAGCTCCAGGC[C/T]TCCAGCAGAATCAGG | 7468 |
rs560100846 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979161 | CTCCTCAGCGTTACC[C/G]CCACACTTGAATTTC | 7468 |
rs560119146 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961230 | GTAGAACTGGACTTT[A/G]CCCTGTGGCAGCGCC | 7468 |
rs560127018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920791 | GTCATCCCAGCACTT[C/T]GGGAGGGTGAGGCAG | 7468 |
rs560196340 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876171 | GTGAGCTGAGATCGC[C/G]CCACTGCCCTCCACC | 7468 |
rs560246463 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968734 | GTACATAGTAACAAC[A/T]AGGAAAGGCTCCCAC | 7468 |
rs560269628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921317 | ATAAAAAATAAGCTG[G/T]GCATGGTGGCGTGCG | 7468 |
rs560269971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955006 | CATGGTTTTGAAGCA[A/C]CTTTGCTCTGAAAGC | 7468 |
rs560281413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952982 | AGTGACTGCTCCACC[A/G]CTGGCCAGCTGCTCT | 7468 |
rs560303196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1893985 | GCCCAGGCTGCAGTA[C/T]AGCGGCATGCTTATA | 7468 |
rs560327551 | snp | C/G/T | 0.00279258 | 0.0372817 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954076 | CTGCAACCTCTGCCT[C/G/T]CCAGGTTCAAGCGAT | 7468 |
rs560354001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971997 | GCAGGACGCTCACGC[C/T]GCTCCTGTACCCCCA | 7468 |
rs560372868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937789 | CTGGGCAGCGCTGCT[C/T]TAGTGCTATGGGGAC | 7468 |
rs560388837 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932883 | CTGTGTCAAGGACCT[C/T]GCCTGTGGGAAAGCG | 7468 |
rs560407671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899502 | CGCTGTTCTAGTCCA[C/T]GGGCATCTCTGGTCC | 7468 |
rs560448780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894875 | ATTGTTATACAACCA[C/T]GACACTGTCTCCAGA | 7468 |
rs560453728 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959144 | CCTGCAGTGTACTAA[A/G/T]CAATCAACACGCTTT | 7468 |
rs560469293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932319 | TGGTGCATGCCTGTA[A/G]TCCCAGCTACTCGGG | 7468 |
rs560500734 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926860 | GCTTTATGTCAGTTC[G/T]TTTTACATGCCTTGG | 7468 |
rs560537858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895915 | GGCTGGCTGGTAGAG[A/G]GGCTCAGGTGATGAT | 7468 |
rs560562157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938627 | GGGAAGGCTGGGGCT[C/G]GTGAAGGGGAACAGG | 7468 |
rs560616251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913591 | AGAAGAAATAATGTA[A/C]GCTGTCCCCTCTCTC | 7468 |
rs560624968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873836 | GTTCATAATCCAAAC[A/G]TATTTTGTCCTGTGC | 7468 |
rs560638369 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889459 | CTGGGCCAACCAGAG[A/T]GCTGGGATTATGGGT | 7468 |
rs560655962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905731 | CCTGTCCTGTGCCAT[A/G]TGTGCTCTGCAGGAG | 7468 |
rs560668333 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913263 | CACCTGTTACTTAGC[A/C]GACCTTGGTCTAGCG | 7468 |
rs560670249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905134 | AAACTCTGTCTCACA[A/C]AAAAAAAAAGAATGT | 7468 |
rs560679552 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884259 | TGCTACTGTGCCTGG[C/G]TAATTTTTGTATTTC | 7468 |
rs560713415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906603 | TCCTGTAGTCTGCAA[C/T]AGCTTCTCTGACATT | 7468 |
rs560726770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899181 | TCAACATTTTTTCAA[A/G]GTTTTACATTTGCTC | 7468 |
rs560729672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912433 | AAACCAAGTTATGTT[C/T]TGTAATTGCATTTTC | 7468 |
rs560732672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920076 | GGTGACTGTGAGTAT[A/T]CTAATAAATCTACTG | 7468 |
rs560771088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887971 | CTGCTCCAGATTGGA[C/T]TCCTCCCTATTCTGC | 7468 |
rs560880864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881788 | TCTAGGTGCATATAA[C/T]AGGGAGGTTATACCT | 7468 |
rs560883776 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924393 | TCAGCCACTCTGGTA[C/T]GTTGCTCGGCTGTGT | 7468 |
rs560900886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893397 | ATCACTTGAACCCAG[C/T]GGCAGAGGCTGTGGT | 7468 |
rs560926324 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939476 | ATGGGGTTCATTGTA[C/T]AGTTTGTCTGCTTTT | 7468 |
rs560947274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973134 | ATAGGTGTGAGCCAC[C/T]GCGCCCGGCCGACAT | 7468 |
rs560982927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931789 | CTATAATTTAGAATA[A/G]CAAGGATATTTAGGA | 7468 |
rs560989563 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910889 | CATGGTCATGCTTGT[C/T]CTTTGTTTCCCAGGG | 7468 |
rs561010068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959988 | ACCTTAGCTTCCCAA[C/G]CAGCTGGGACTACAG | 7468 |
rs561022151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967515 | CCTGGGAGGCAGAGG[C/T]TTCAGTGAGCCGAGA | 7468 |
rs561051145 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936528 | ATACAAAAATTAGTC[A/G]GGTGTGGTGGTGCAT | 7468 |
rs561070783 | snp | C/T | 1.67539e-05 | 0.00289425 | missense | WHSC1 | GRCh38.p7 | 4:1978806 | ACTTAGGGGCGGCAT[C/T]GGTCAGAAGCACCAA | 7468 |
rs561090757 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941871 | TTTGTGATGTTTCCA[A/G]TGCTGAATGCCTGTT | 7468 |
rs561104845 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974297 | CTCTCTGTAACCTCC[A/G]CCTCCCGGGTTCAAG | 7468 |
rs561114051 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967084 | AAATCAGAACTGGGT[-/G]TGTGAAGACATTATT | 7468 |
rs561118821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873755 | GTAGCTGGAATTAGG[C/T]TTACTAAGCTACAGG | 7468 |
rs561121261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926224 | CAGAGGCATGATCTC[A/G]GCTCACTGCAACCTC | 7468 |
rs561142680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899030 | TTTTACCTTGGGACA[A/G]TTGGTATGATATGAG | 7468 |
rs561209149 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872314 | TCCTTGAAGCCTCAG[G/T]GCATGAGATGGGACC | 7468 |
rs561229956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966570 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCGGGA | 7468 |
rs561232877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952031 | CCACTGGAGACAGAA[G/T]CAGACGGCTTCCCTT | 7468 |
rs561255153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905087 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCTAGT | 7468 |
rs561259808 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931152 | CCTTCAGGCCTGTGA[C/T]TTCCGAGGAGGCAGC | 7468 |
rs561295988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959038 | GGGGTGGACTCCCAT[G/T]TGGCTTGCTGCTGGT | 7468 |
rs561297340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891202 | CCCCGCCTACGTGGA[A/G]TTGTTTTATATGAGA | 7468 |
rs561303160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937228 | AGCTAATTTTTTTGT[A/G]TTTTTAGTAGAGATG | 7468 |
rs561303266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945696 | AAGTCCTTGGCTCGT[G/T]TGATCCAGTTGAGTT | 7468 |
rs561316838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978441 | TTAGGGGCCTGGCAG[A/G]TACTGTGGAGTCAAC | 7468 |
rs561368504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944827 | AAAAATTAAATGTCT[G/T]TTTTCAGCATACTGA | 7468 |
rs561459225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912270 | AGACATTTTCTGTTA[A/G]CTTTCTATCATGGAA | 7468 |
rs561473236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919132 | ATGGCATCACTGCAC[C/T]GTAGCCTGGGTGACA | 7468 |
rs561510739 | snp | C/T | 0.000628515 | 0.0177162 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976472 | CTTAATTCTTGACTC[C/T]AGACCTCGACGACCC | 7468 |
rs561701996 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1890108 | GTATCTAGCTTCTTT[A/C]ACTTAGCATCATGTT | 7468 |
rs561702592 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969887 | AGGATTGGGAACTTG[A/T]AGAACTCAGGAGTGA | 7468 |
rs561704737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948355 | GACTATGTTGGGACC[A/G]TACAGGTGAATGTGC | 7468 |
rs561725902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902098 | TCTATAGGGTGTTGC[A/T]TTTTAGTTGTAACTC | 7468 |
rs561742670 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896859 | TCTTTTCTTTCTCCT[A/T]GCCTTCCCCAACATA | 7468 |
rs561764172 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940884 | ATAGAGCTCTGCGGC[G/T]TGCCACTCTGAATCC | 7468 |
rs561765616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968794 | GAGGAGACACAGGAG[A/G]CAGCATGGAGAGGAA | 7468 |
rs561805326 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921144 | CTTTCATCAAGGATA[G/T]TACACATGAAACTTT | 7468 |
rs561807336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933380 | CAGGGCAACAGTGTC[C/T]TTCTGCAAGATGTTT | 7468 |
rs561817918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955511 | ATTGTAATCATTTCG[C/T]AAACATACAGGAAAT | 7468 |
rs561851044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902631 | TTGTTTTGAGACAGG[A/G]TCTTGGTATGTTGCA | 7468 |
rs561867554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916310 | AAAGGAGTGCATTTA[G/T]TCAGCTAGCTAGCTT | 7468 |
rs561871095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932806 | TGTTTCTGTAAGAAG[C/T]GGCTGCTGCCTCATC | 7468 |
rs561872600 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876601 | GGTGGCTGAAGTGGG[A/T]GGTCACCTGAGTCCA | 7468 |
rs561877147 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907127 | TAATGAACTTAATCT[C/T]GCTAAGCTTCAGTTT | 7468 |
rs561897083 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904184 | GTAGTGATTGGATGT[G/T]TTAGTGTTTGTCTTC | 7468 |
rs561928940 | snp | C/G/T | 0.00795819 | 0.0626103 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915715 | CATTAGAGGGTCTGA[C/G/T]TGGCCATTGACCACT | 7468 |
rs561987743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921452 | GACAGAGCGAGACTC[C/T]GTCTCAAATTAAAAA | 7468 |
rs562000026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927209 | GCTTTCTCCAGAGTA[A/C]GTGATCCAAGAAAGA | 7468 |
rs562043271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938764 | TGGCTAAATTTTATT[A/G]AAGTTACTTTTTACT | 7468 |
rs562098863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921874 | CAATATTAGGCCGGG[C/T]GCGGTGGCTCACGCC | 7468 |
rs562121226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975887 | CAGATCTCATTGACA[A/C]TGACCCTATTTCCAA | 7468 |
rs562124371 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979878 | GGGCGTGAGACCGCA[A/G]TCTGCTTAGAGCACA | 7468 |
rs562139656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896213 | GCTCTGTGCAGGCAG[C/T]CCAGTCAGGCCCAAG | 7468 |
rs562150266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902003 | GGATGAGTATAAGCC[A/G]TAGGAAACAACCAAG | 7468 |
rs562209628 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980615 | GGTTCAGGGGTGTGT[A/G]GCCCTGCAGGGTCCC | 7468 |
rs562251797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946605 | AAATATTCTGATTCA[C/T]ATTTTAGGACTTTTT | 7468 |
rs562252470 | snp | C/G/T | 1.70863e-05 | 0.00292281 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953515 | CCTTCAAACCCAAGG[C/G/T]CGTCAAAAGGTACAG | 7468 |
rs562268525 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956995 | ATTTTAAAAAATTAT[C/T]AAGAGGGCGAGACGA | 7468 |
rs562274441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900367 | ATTAGTGGTATGACT[A/G]GAGTGTGCTGTCTTG | 7468 |
rs562323675 | snp | C/G/T | 6.59527e-05 | 0.0057422 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900927 | GTTTAATGGAGAACC[C/G/T]GGCGCACACGATGCC | 7468 |
rs562324621 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980758 | AGCCACTGACTTGCT[C/T]GCGCGGCCGTGGCCT | 7468 |
rs562340439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902573 | GAACCTCATGCTTTT[A/G]CTTGGGAAGAGGCCT | 7468 |
rs562356772 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932125 | CATTGTCACGCGCCC[A/G]TGACCTCAGTGTTAG | 7468 |
rs562429435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969738 | ATCCTGACCCAAAAC[A/T]GCAGAACTTCCTTAC | 7468 |
rs562436148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907327 | TCCTGAAAACCTTCA[C/T]GTTTGACCAGTTATT | 7468 |
rs562437393 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869496 | GCGATTACAGATGCC[C/T]GTCACTATGCCTGGC | 7468 |
rs562477311 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935885 | CAAACAAAAAAACCC[C/G]CAAACACCATAACCT | 7468 |
rs562502182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949071 | GGCCACTGCTTCCCC[A/G]TGCCCTGTGCTCCCC | 7468 |
rs562507876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975177 | GAAAGGCCATGGGTC[A/G]AGCCAGTACAGATAC | 7468 |
rs562524741 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907798 | TTGTATTTTTAGTAC[A/T]AATGGGGTTTCACCA | 7468 |
rs562525708 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892569 | AGAAAACCACTGATA[A/C]CTCTTTTTTTTTTTG | 7468 |
rs562568907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948267 | TGTGTCCGCTCAGTC[C/T]CTGCACTTTTCCTTT | 7468 |
rs562576029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908321 | AGAAGAAGGGAGTGT[A/C]CTGCACCAGCATAGG | 7468 |
rs562586150 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915139 | TTTTTTTTTTGAGAC[G/T]GAGTCTGGCTCTGTT | 7468 |
rs562593417 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966942 | TCAAGTTATAACATT[A/G]TATAGAGAATTGGAA | 7468 |
rs562612658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955464 | TTCTGTGCGTCTTCA[C/T]GTTAATAGTATATCA | 7468 |
rs562625629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961243 | TTGCCCTGTGGCAGC[A/G]CCAGCATTTGTCTCC | 7468 |
rs562686689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915609 | TCCCTGGGTCCAGGG[G/T]TTCCTTGGTGCTGGG | 7468 |
rs562710566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967375 | ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 7468 |
rs562746401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954282 | GAGCCACCACGCCTT[A/G]CCAATTTTTGTATTT | 7468 |
rs562789014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927154 | CATGTGGCCCTCTCC[A/G]CAGGGCTGCTGGTGT | 7468 |
rs562824105 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945781 | GTCTGGGCCTGAGAC[G/T]TGCATGGAGGGCTGT | 7468 |
rs562832854 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932470 | AAAAAATTCCAGCCC[G/T]GCGCAGTGGCTCCCG | 7468 |
rs562839376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945812 | AAAGCCACGGATTCC[C/T]CTCGCTGGAGAGGCT | 7468 |
rs562845144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938696 | GAAGGAAAGGAGGTT[C/G]TCCTGTGGTTGAAAA | 7468 |
rs562852381 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953061 | TGCCAGTTAGACTGG[C/G]CCTCCCCAGCCAGGC | 7468 |
rs562858823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889765 | ACCCGCCTTGACCTC[A/C]CAAAGTGCTGGGATT | 7468 |
rs562902739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972460 | AGCCAGTGCTTTATC[C/T]TGAAGCCTTACTGTG | 7468 |
rs562923839 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959906 | CACTCTGTCATCTAG[A/G]CTGGAGGGCAGTGGC | 7468 |
rs562964139 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913489 | TCCACTTTCATGTTC[C/T]GCCCTGTACATCTGG | 7468 |
rs562991262 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939202 | AGTTAAACAGACTTT[A/T]AAAAAAAAAAAAGAC | 7468 |
rs563003059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936095 | CAGGAAAAGTGCAGC[A/G]TAGATACAAAGCCAG | 7468 |
rs563055316 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921610 | AACATGGTGAAACCC[A/C/T]GTCTCTACTAAAAAT | 7468 |
rs563081000 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899583 | CTCAGAGGGCTGTTG[A/T]TGGAGCTTGTGATGG | 7468 |
rs563100437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886109 | GCGTCCATTGAAGAC[A/G]TATGCTTTGTGAGTC | 7468 |
rs563108105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906575 | TCTTTTCCCTGCCTT[C/G]GAGTTAAGTAATTCC | 7468 |
rs563125080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909316 | GCCTAGGTTCTTTGA[A/G]TACAGAATAGTATGT | 7468 |
rs563141533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977985 | TAGAAAAATTAGCTG[A/G]TCGTGGTGGCGGGCG | 7468 |
rs563169469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914132 | GGTTCAAGTGATTCT[C/T]GTGCCTCAGCCTCCC | 7468 |
rs563237190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942210 | CCTGAGGAAGAGAAT[A/G]AATTAAAATTACACA | 7468 |
rs563240402 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957531 | GACCTCAGGTGATCC[A/G]CCTGCCTCGGCCTCC | 7468 |
rs563277370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949467 | GACGGAAGCCCTTGG[A/G]AAAAGCCCACTCTGG | 7468 |
rs563296619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892611 | TGCCCTGTCGCCCAG[A/G]CTGGAGTGTAGTGGC | 7468 |
rs563318589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885709 | AGGAGCTGTTACTGC[C/T]TCTCTTGGTACCCAT | 7468 |
rs563347541 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892598 | TGAGACGGAGTCTTG[C/T]CCTGTCGCCCAGGCT | 7468 |
rs563355432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929992 | GAAAGTGCAGATTCC[C/T]GGTAGGCAGGTTGGG | 7468 |
rs563397813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923095 | TTTATGAACTTGGCC[A/C]GCATGGGAGAGGAGC | 7468 |
rs563405496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910335 | GGTTCAAGTGATTCT[C/T]CTGCCGCAGCCTCCC | 7468 |
rs563410143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916527 | ATTTTTGCATTTTTC[C/G]TAGAGATGGGCTTTT | 7468 |
rs563447846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957624 | GTCTGAGAACAGCAA[A/G]TCCCAGGCTTTGACC | 7468 |
rs563468942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898243 | AGGTGCACATCACCA[C/T]GACTGGCTAATTTTT | 7468 |
rs563479926 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982518 | CCCAGCCCTGCAGTC[A/G]GCTGAGCCGGGTGGT | 7468 |
rs563481941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897616 | AAGATCCCGTCTCTA[C/T]AAAAAATTTTATTTT | 7468 |
rs563499775 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969426 | AAACCCCAGCCAGGT[G/T]CAATGGCGTGTGCCT | 7468 |
rs563522149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922562 | GTAAGTGGATGCTGC[C/T]GTGGCCACATTTGAA | 7468 |
rs563529027 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874018 | ACAGGCACACTCAGC[C/T]TTCCTGGCTCTGCCC | 7468 |
rs563569628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903665 | TTTATATAGAGATCT[C/T]CAAAATGTTGAACAC | 7468 |
rs563643916 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870759 | GGAAGAGCACGACGC[A/C]CTGCCCTGCCCCGTC | 7468 |
rs563648789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929131 | GGTGGGTGGGCATTG[G/T]TGGGTGTTGGTGTCC | 7468 |
rs563670751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896809 | CTTTCTCTCTCATTC[A/T]TTCTTTCTTTCTTTT | 7468 |
rs563676117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885073 | CGAGATCATGCCATT[C/G]TATTCCAGCCTAGGT | 7468 |
rs563677800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963106 | GCCCCAGTGACTCTT[C/T]AGCAACACCCTCATA | 7468 |
rs563696275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976875 | CTAGATCTCTGCATC[A/G]AGCAGAGAAGATATG | 7468 |
rs563720335 | in-del | -/CCTC | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896665 | AACCACTGTGCCCGG[-/CCTC]CCTCCCTCCCTCCCT | 7468 |
rs563733723 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905939 | AGCTGTCTCCCCTTT[C/G]TCTGAGGATGGACCT | 7468 |
rs563740019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976995 | GGGCGGGGCGGCCAG[A/G]AAGGAGGCGACGCTG | 7468 |
rs563758150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963844 | CACAGACCCTCATCT[C/T]TACAAAAAAGAAAAA | 7468 |
rs563759250 | snp | G/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870368 | AGCAGACACTAAGGC[G/T]CAAGGCCGAAGGTGT | 7468 |
rs563820340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971257 | AGGAGTTGTTCTCAG[A/T]CAAGGCAGAATTCAG | 7468 |
rs563848588 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933483 | CAAGCTCCGCCTGGC[A/G]GGTTCATGCCATTCT | 7468 |
rs563867324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884451 | CAGGCTGGAGTGCAG[C/T]GGCCCAATCTTGGCT | 7468 |
rs563879434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891897 | CAAACAAAAACGAAA[A/C]AACGAAAAACCTCAC | 7468 |
rs563901259 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949784 | AAAAAAAAAAAAAGC[C/T]CACTCTAACACTACT | 7468 |
rs563910483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976345 | GAGGAGGACACTCCT[C/T]TCCTCTCCTCTTAGT | 7468 |
rs563952236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935556 | TAGATTGGACAAAAT[C/T]GTCACTAAAAATAAC | 7468 |
rs563993205 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940830 | TGTAGGCCTTCCAGT[G/T]CAGGAAGGTCAGGGA | 7468 |
rs563998767 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899062 | TGGAAGAGGAACTGA[C/T]TTTGATCTACCTTTT | 7468 |
rs564013708 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943145 | TCGGGGAGCAGCCTG[G/T]TGTCCTGCCCCAGGT | 7468 |
rs564014869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956994 | GATTTTAAAAAATTA[C/T]TAAGAGGGCGAGACG | 7468 |
rs564052769 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981165 | TATGATTTTTCTGAA[G/T]GAAATAATGCAAACA | 7468 |
rs564077909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956281 | TGATCTTTATAGAAA[A/G]TACTGGACTAAGCAT | 7468 |
rs564086594 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898090 | TGAGGCTCTGCTTCC[G/T]TTTTTTCCCCCTTCT | 7468 |
rs564087924 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917374 | CTGGTTTAAAGAAAC[A/G]ATAAAGGTATTATGT | 7468 |
rs564099175 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929407 | TGTTACTGCCCCCGT[A/T]TCACAGAGTGGAGGC | 7468 |
rs564124419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896951 | CAAGGCGGGTGGATC[G/T]CTTGAGCCCAGGAGT | 7468 |
rs564130337 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891623 | TTTGGGAGGCTGAGG[C/T]GGGCAGTTCACGAGG | 7468 |
rs564179690 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889105 | GTTTCGCCATTTTGG[C/T]CAGGCTGGTCTGGAA | 7468 |
rs564191942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928498 | ACCATACAGTTTCAC[C/T]GTGAAGCTCGGAGAC | 7468 |
rs564201122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934974 | CACCAGTTTTTTTGT[G/T]GTAAAGAGATTTGAT | 7468 |
rs564216038 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870624 | TCTACCGCAGCGGCG[C/T]TGGGGTAGCGCCCCT | 7468 |
rs564244848 | snp | A/C | 0 | 0 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981723 | ACATCTAAACCCCGG[A/C]GTGTGCAGTGCCCAT | 7468 |
rs564256302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927754 | AAAAAAAAAAAGCCG[C/T]GTAGGGAGCAGGCAG | 7468 |
rs564271988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903585 | ATTCTGTGAGAATTC[C/T]TTTTCGACCAGTTGA | 7468 |
rs564282690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902799 | ACTTGAGTAACTCAA[C/T]CTGAATTTTGACTCT | 7468 |
rs564290318 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869488 | GAATAGTTGCGATTA[C/G]AGATGCCCGTCACTA | 7468 |
rs564330895 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974272 | CTGGAGTGCAGTGGC[A/G]CGATCTCCACTCTCT | 7468 |
rs564335268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961957 | TCTAGCAGGAAAGTC[C/T]GGCTATTTTTAAAAG | 7468 |
rs564364934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933426 | GAGTCTTGCTCTGTC[A/G]CCCAGGCGGCTGGAG | 7468 |
rs564376942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921914 | AACACTTTGGAGGCC[A/G]AGGTGGGTGGATTAC | 7468 |
rs564410335 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870149 | GAAGGGACAGCAGCG[C/G]AGGCGGCGCGGGAGA | 7468 |
rs564429417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932897 | TCGCCTGTGGGAAAG[C/T]GAGGCGCGGGGCTGG | 7468 |
rs564468265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901846 | TCTTGGTTCCCAGTG[C/T]AGAGCCCAGCACACT | 7468 |
rs564472093 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925773 | ATATCTATATATATA[-/T]TTTTTTTTGTTTGTT | 7468 |
rs564519941 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970586 | TGGGAGGAGCAGGGA[C/G]AAAGGAGGGTAAGTT | 7468 |
rs564527822 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949534 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT | 7468 |
rs564540624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1890009 | CTCCTCTCCCAGCCC[C/T]TGGCAGCCATTCTAC | 7468 |
rs564543264 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978308 | CTTGGGAGAGGGCAG[A/G]TCACATGGAAATCAG | 7468 |
rs564553627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877414 | TGGCTTTCTGACTCT[C/G]ACTGCACTACTTGTT | 7468 |
rs564553642 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884384 | TTACAAGTGTGAGCC[A/T]CCGCAGGCCCCTTTT | 7468 |
rs564579872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919929 | GACAGAATGAGACGC[C/T]GTCTCAAAAAAAAAG | 7468 |
rs564611854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883880 | GGAGCTGCGTTGCTG[C/T]CTCTTGTTCTCTGTT | 7468 |
rs564647195 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970905 | AAAGGCTGAAAGCCC[A/G]TAGAAACAAGCAAGA | 7468 |
rs564656391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975916 | AAATACAGTCACCTT[C/T]CAAGGTTCCAGGAAG | 7468 |
rs564659274 | in-del | -/TAGAGTG | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906707 | CTCTGTCTCCCAGGC[-/TAGAGTG]TAGAGTGCACTGGCG | 7468 |
rs564693472 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980716 | CAAAGTTAACTACAC[A/G]GAGGACCCAGGGGAA | 7468 |
rs564710062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913466 | TGCTTCAGCGGTCAC[A/G]CTCCTGGTCCACTTT | 7468 |
rs564716886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896161 | TGGTGCTCCTAATCA[C/T]GGCAGCCAGCTGCTC | 7468 |
rs564789936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940004 | GCACACAGTGTCTGT[A/G]TACATGTACAGATAT | 7468 |
rs564858193 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872789 | GGGTTATATTCACTC[-/TA]TTTTGTGTATTTCAA | 7468 |
rs564864503 | snp | C/T | | | missense | WHSC1 | GRCh38.p7 | 4:1901000 | CCCCCTAACACTACC[C/T]CTATCAAAAATGGCT | 7468 |
rs564865732 | snp | A/G | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1893841 | TGAGCCACTGCACCC[A/G]GCCCTTGCCTCATGT | 7468 |
rs564889979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886817 | GCACTTGAGCCTTGG[A/G]ACAGAGCGAGACTCC | 7468 |
rs564922868 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941684 | AGTGTGCATCATGTT[C/T]CTTATATGAAAACGT | 7468 |
rs564934340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905060 | GCTAGAACCCGGGAG[A/G]TGGAGGTTGCAGTGA | 7468 |
rs564936307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898543 | GTGGTGGGCGCCTGT[A/G]GTCCCAGCTACTCAG | 7468 |
rs564948798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904550 | CATTTCTTTTTATAT[C/T]CAACTCAAATATGTA | 7468 |
rs564998322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973718 | TGTGTCAGAGGCCGC[A/G]TGTGAATAGTGACTC | 7468 |
rs565009542 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931652 | GGTCTGGCCACATGT[G/T]CCTGCTGTCACCTTT | 7468 |
rs565016884 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881324 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 7468 |
rs565036406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887836 | GTTACTAATTCAGCC[A/T]AAAGTTTTTCAAATG | 7468 |
rs565037086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973235 | AGGGTCAAGACATGG[C/T]GGGCAACCCACAGAT | 7468 |
rs565042993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873171 | TGGGCTGATGGTTGG[C/T]AGAGTGAGGACTTAC | 7468 |
rs565070861 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946068 | GATTCATCACCTTAG[-/T]TTTTTAAAAAAAATC | 7468 |
rs565074155 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942650 | GTGGTCAATGTAGAT[G/T]TCAAGTTGAAAGGCA | 7468 |
rs565105102 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880320 | TAGAACTCCTGCAGG[G/T]CCTGACCTCTGATTC | 7468 |
rs565105924 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909068 | AATGAGCTCCTCCCT[-/A]AAAAAAAAAAGAGTT | 7468 |
rs565118825 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932119 | CCACATCATTGTCAC[A/G]CGCCCATGACCTCAG | 7468 |
rs565142191 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926686 | ATATTGGCTAGGCTG[G/T]TCTCAAACACCTGAC | 7468 |
rs565150625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972423 | TTTCAAAGTCCATGT[A/G]GAAGGAAAGATCTGC | 7468 |
rs565170659 | in-del | -/ACACACACACA | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951444 | TACACATCATGTAAT[-/ACACACACACA]CACACACACACACAC | 7468 |
rs565183325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944767 | CTTCTAAAATTGCCC[C/T]ACCTGCTCTAGATGG | 7468 |
rs565188163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936207 | CAACCAAGGAAACAC[C/T]GGGTTATTCTGTCTA | 7468 |
rs565197119 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901971 | TTCACGTGGCACTCG[C/G]GATGGCCCTGACACT | 7468 |
rs565206830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911404 | ACCAGCCTGGCCAAC[A/G]TGATGAAACCCTGTT | 7468 |
rs565216710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892726 | GGCGTGCACCACCAC[A/G]CCTGGCTAATTTTTT | 7468 |
rs565258036 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891713 | AAAATAAAAATTAGC[C/T]GGGCGTGGTGGTCGG | 7468 |
rs565355126 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951283 | CGAATTTGTAGTGTC[G/T]TTTCCCTTCCCACCA | 7468 |
rs565418549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950789 | TTGGATGTTCATAAC[A/G]CTTCCTTCATTTTAA | 7468 |
rs565445783 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872458 | TATAGGACCCATTGC[A/C]GCACGAATCTTTCTG | 7468 |
rs565465311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964819 | GGGGAAAATAAGAAA[A/C]TTTAGAAAATTAGAC | 7468 |
rs565486353 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954011 | TTTTTGGAGAAAAAA[A/T]ATCTCCCTCTGTTGC | 7468 |
rs565488441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964637 | GGTGCGCTGCGCTGC[C/T]GTTGTTATCACACCT | 7468 |
rs565518040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924361 | GGGTAAGGCGGTGTC[A/G]GGTGGGAACCGCCCC | 7468 |
rs565529207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964317 | GGAAGCTGTGTCCCC[A/T]CCTAGACCACAGTTG | 7468 |
rs565542742 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872747 | AAGCCTTGATTTTTA[A/T]ATGAGTTAAACGCCA | 7468 |
rs565591313 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929923 | ATTACCAGGTGGAGC[A/G]AAGTCCCCAGGATCA | 7468 |
rs565620998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950914 | TATCACAAAAACCAG[C/T]TGATGATGGTTCCAC | 7468 |
rs565626742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929688 | GTCATGAAATATTAT[G/T]ATGTTTTTCAGACAT | 7468 |
rs565655174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911646 | ATTGCATAGGAAGGG[A/T]GGATTACTAATAACA | 7468 |
rs565672941 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906820 | TGTGTGCCACTATGC[C/T]TGGCTAATTTTTGTA | 7468 |
rs565679845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879850 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTTTTCTC | 7468 |
rs565729067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910932 | TCATGTCGTTGTGAC[C/T]TTGCTCCTGTGCTCC | 7468 |
rs565821116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879241 | TTTATTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 7468 |
rs565869550 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971618 | CACATGTACTGAGGC[A/G]TGAGGTCCGAGCCAG | 7468 |
rs565893569 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923396 | ATTCTGTAAAGAGCC[A/G]AAACAATTCTGAAGG | 7468 |
rs565900267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885388 | GCTGATTCAGAAAAA[A/G]TAACAACAGAATGAA | 7468 |
rs565909301 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973717 | TTGTGTCAGAGGCCG[C/T]GTGTGAATAGTGACT | 7468 |
rs565926521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977110 | GTGGGAATGGAGGGG[C/T]CCAGAGCCCCTGTCC | 7468 |
rs565942847 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934076 | TTAGTAAGGAAAAGA[-/T]TTTTTTTTTGTTTTT | 7468 |
rs565944724 | snp | G/T | | | missense | WHSC1 | GRCh38.p7 | 4:1976662 | TGTCCTGCCTGGGCC[G/T]TGGCAAGCGGCCCTT | 7468 |
rs565971319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908705 | GCTCTCTGTGGAAAG[A/G]CACAGGTCCCCATTG | 7468 |
rs566006824 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875143 | ATTTTAAAATTTTTT[A/G]TGGAGTCAGTCTTGC | 7468 |
rs566009959 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891781 | AGAATGGCGTGAACA[C/T]GGGAGGCGGAGCTTG | 7468 |
rs566020260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949877 | ATGTCAGCTAAATGT[A/G]GAAAAGCTCACTGAT | 7468 |
rs566077048 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981905 | CACAGCCTCACCATA[A/C]CCTGTTGAGGTGTGA | 7468 |
rs566106089 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870308 | TCGCCAGGCTCCCCT[A/G]GGCCCGCTTCTCAGC | 7468 |
rs566129789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903065 | GGTCCCAGCTACTAG[A/G]GAGGCTGAGATGGGA | 7468 |
rs566141173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900450 | ATCATTTTGTGATTC[C/T]GTGTAATTTTTGTGA | 7468 |
rs566141905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941331 | TTGCTTATACTGTTG[C/T]CAGGTACAGTAGAGA | 7468 |
rs566204139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899922 | TGTTTAATTTAGGCC[C/T]GAACACGGAGGGGAT | 7468 |
rs566273763 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890862 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGGG | 7468 |
rs566292998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963216 | GCAGGTCCATAAGGG[C/T]GAGAGTGGGTTTGTA | 7468 |
rs566317317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906141 | TGGGGATATTTACTT[A/T]TTTATATGATGCCAT | 7468 |
rs566320103 | in-del | -/C | 0.00288553 | 0.037874 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938426 | CTTTCTTTTTTTTTT[-/C]TTTTTTTTTTTTTTT | 7468 |
rs566353798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894459 | CCTACCACTTTGGGA[A/G]TCCAGGAGTTTGAGA | 7468 |
rs566387782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922103 | CGTGAGCTGAGATCA[C/T]ACTACTGCACTGCAG | 7468 |
rs566402125 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877688 | CATTCTCATTCTGTT[A/C]CAGCCACACGGGCCT | 7468 |
rs566425358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938252 | GAGATTGGGCAACCA[C/T]GGATGACTTATGTGT | 7468 |
rs566430915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938844 | CAGAAGTTTTCAGGT[G/T]TCTTACTTGATGGTG | 7468 |
rs566450813 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979513 | GCTGGCCCTGCAGGT[C/G]GTGGCAGCAATGGTG | 7468 |
rs566454589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977862 | CAGGCACGGTGGCTC[A/T]TGCCTCTAATCCCAG | 7468 |
rs566486580 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979036 | ACAGACGTACAGGCC[G/T]CCTCGGGAGGGAGCG | 7468 |
rs566537546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946666 | TACCATTTTTATTGT[C/T]TTATGTAGAATGTTA | 7468 |
rs566573299 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948619 | ACTATTGTAAGGTCT[A/G]TATTCTGTATGTGGG | 7468 |
rs566588746 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870337 | GCGAGGGCTCAAGCT[A/G]GGCCTGTAAAGCTCG | 7468 |
rs566589431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978506 | GACAGTTTGTCTGCC[C/T]GTCCTGTTCGCTGGA | 7468 |
rs566632628 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932741 | ATGGCCAACAGGAGC[A/G]AAACTCCATCTCAAA | 7468 |
rs566636834 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928630 | GCTGTCTTGTGAGGC[A/G]AGGTGGCTGCAGGGC | 7468 |
rs566650649 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955108 | TAGTTGCTCTTTTCA[C/G]TATGACTGGAGTCAG | 7468 |
rs566677273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919508 | CCCCACTTCCCACTT[A/T]TGGTTATGTTACTTG | 7468 |
rs566688538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952701 | AAGAACAGCTCCAGG[C/T]TTGTCCTGGGTTGTC | 7468 |
rs566695931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874121 | TAAGGCTTTTTACTC[A/G]TATATTCTGATCTAC | 7468 |
rs566707347 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913740 | ACAATAAATAACAGC[A/G/T]CAGCCAGACATTCAG | 7468 |
rs566711039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920108 | ACATGATTTTTTTGT[C/T]CCTATATGGGATCTG | 7468 |
rs566740912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967134 | AAAAGGATTATAAGA[C/T]AGTACTGTGAACAAC | 7468 |
rs566761012 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963747 | AGCTGGGCACAGTGG[C/G]CCACGCCTGTAATCC | 7468 |
rs566775708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973389 | CCATGTGCATGCCCC[A/G]TGCTGTCCTCGTCCC | 7468 |
rs566784220 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927415 | GAAAGCAAAAGAAAA[-/CT]CTAAAAAGATGTTGG | 7468 |
rs566785759 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926084 | CTGGGATTACAGACA[G/T]GAGCCAGTGCACCTG | 7468 |
rs566785811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967594 | AAAAAAAAAAAAAAG[A/G]TATTTCCAACTTAAC | 7468 |
rs566797811 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968326 | GGATGATGATGACTG[C/T]GAGGCAGGAAGGAAG | 7468 |
rs566820794 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918850 | TCCTAATGTGGATAA[A/G]AAGATACCGAGAACA | 7468 |
rs566866745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951586 | CTGATGACATGCACA[C/T]TGGACAGGCCAGGCT | 7468 |
rs566894356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937519 | TAGCTCCTATCTCAG[A/G]AGATAGCACATGATA | 7468 |
rs566899649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925243 | CTTGTCAGTTAACCA[A/G]TGGCCAACCCTTGAG | 7468 |
rs566918810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972962 | GGTTCAAGCCATTCT[C/T]CTGCCTCAGCCTCCC | 7468 |
rs566943306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892886 | ACCACTGGTAACTCT[A/T]AACTGGTAATTTTTG | 7468 |
rs566946832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924874 | CGAGGCTGCAGTGAG[C/T]CATCATTGCGCCACT | 7468 |
rs566955351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898650 | GGGTGACAGAGCGAG[A/T]CTCCGTCTAAAAAAA | 7468 |
rs566984461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893549 | TTGTTTTTTGTTTTT[G/T]TTTTTTTTTTGTTTT | 7468 |
rs567021252 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933329 | CTGGTGTCTCCTGTC[C/G]CAACAGTAGTGAGGC | 7468 |
rs567029039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944308 | TTGAAAGAACTTAGG[A/G]AGGACCATTGGCTTG | 7468 |
rs567102316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912549 | TTTCAAGTATTCATC[C/T]CCTCATCCTTAAAAC | 7468 |
rs567122079 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969523 | AGCCTGGGCAACACA[A/G]CAAGGCCTTGTCTCT | 7468 |
rs567138947 | in-del | -/T | 0.0726307 | 0.176182 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876754 | GTGTAGAAAAAATGC[-/T]TTTTTTTTTCTGGAA | 7468 |
rs567156338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899324 | GACATCTCGGGCCGC[A/G]TAGCCCTGTTGCGCG | 7468 |
rs567162945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911853 | ATTTTACAAACTTGG[G/T]ATCAGATTACAATAA | 7468 |
rs567175402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918841 | AAATATCCTTCCTAA[C/T]GTGGATAAGAAGATA | 7468 |
rs567196799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943668 | GATGGTCTAGGAGCA[A/G]TCTAAGCTGTGTTAC | 7468 |
rs567217581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905303 | GCGATGTGGCGAGTG[C/T]GGAGTTAGAACTGAG | 7468 |
rs567225178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945816 | CCACGGATTCCCCTC[G/T]CTGGAGAGGCTCCTG | 7468 |
rs567233968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945317 | AGGAGGGAGGATGCT[A/G]TGTGAGAGCCATGCT | 7468 |
rs567245815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899667 | TTCCTAGCTGTGTTT[C/T]GGGGCTCTGGCCCCT | 7468 |
rs567259886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906020 | TGCTAATTCTTTCTC[C/T]GCTTTCTAAAACCAG | 7468 |
rs567277877 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928771 | GAGGGCAGCAGGCCC[A/G]TGAAGGAATGTGCTG | 7468 |
rs567295274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952599 | AAGGGTACAGGTAAC[C/T]TGGTTGGTCACCGAA | 7468 |
rs567337362 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892779 | TCACCATGTTGGCCA[C/G]AGTGGTCTTGAACTC | 7468 |
rs567451109 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897770 | TAGCTGGGATTACAG[A/G]TGTGTGCCACCAAGC | 7468 |
rs567469784 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922052 | ACTCAGGAGGCCGAG[G/T]CAAGAGAATTGCTGG | 7468 |
rs567470552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958787 | TCAGAGAGTATGAAA[A/T]GTTTAGATTCTTGGG | 7468 |
rs567471166 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924810 | TGCACACTTGTAGTC[G/T]TAGTTACTCAGGAAG | 7468 |
rs567476763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881343 | TCTCGGCTCACTGCA[A/G]CCTCCGCCTCCTGGG | 7468 |
rs567488430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967056 | AAAAAAAGAGAAAAG[A/G]CTCACATAACTAAAA | 7468 |
rs567510059 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925174 | ACCTAGGTCTTTCTA[C/T]ATTGTTTTTTATTTT | 7468 |
rs567510968 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879249 | TTTGAGACGGAGTCT[C/G/T]GCTCTGTCACCCAGG | 7468 |
rs567522571 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937630 | CTGAGCACTTCTGAC[A/G]TGCTAGGCACTGTCC | 7468 |
rs567522943 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872712 | CTCTTCAGTGCTACC[C/T]ACCTGCTTCACAGAC | 7468 |
rs567541792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873607 | TCCTAATCCTGTGGG[G/T]CTTACATGGGTACAG | 7468 |
rs567572204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978205 | AGAGAAAAGTGTTGG[C/G]CATGGGTGCGAGAGG | 7468 |
rs567577671 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893464 | GGCGACAGAGACTCC[A/G]TTTCAATAAAAAAAT | 7468 |
rs567638439 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891806 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 7468 |
rs567659588 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933690 | TGAGCCACCGCGCCC[A/G]GCCCTGCAAGATGTT | 7468 |
rs567665476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885976 | TATAATCAGAAAATA[C/T]ATTTTATGAATAATT | 7468 |
rs567668202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872513 | AAGTGGAAACATAGT[A/G]TCAAAACTGATGTGG | 7468 |
rs567708912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977803 | CTCAAAAAAAAAAAA[A/T]ACCAAACAAACAAAA | 7468 |
rs567731168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890764 | CCACCACGCTTGGCT[A/G]ATTTTCTATTTTTAG | 7468 |
rs567735327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883662 | AAAGCGTACCTCCTC[C/T]GCTCTGCTGATCCCA | 7468 |
rs567760835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936368 | TTTGTTTGAATTTCT[A/G]TTTTATTCGATAATA | 7468 |
rs567767715 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904133 | GTGTATTTGGACATT[C/G]TAGCCTGGTGAATCC | 7468 |
rs567774525 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980868 | AGAAAATACTGGATC[A/G]GCTCATAGATTTATG | 7468 |
rs567830975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910828 | TTTCTGCTTTACCTA[C/T]TTTGGGGCTCTGGTG | 7468 |
rs567833441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943459 | TCTATTTTTATCCAA[A/C]AGTATAAATTTTGCT | 7468 |
rs567911260 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980320 | TGGAGCACCCTGAGA[A/C]GGGGGCACCATGTGT | 7468 |
rs567923470 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958614 | GTGGCCGTTCCTGAC[C/G]AGTGTTTGTGATAAG | 7468 |
rs567925462 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919497 | GGAGTTGGGTTCCCC[A/C]CTTCCCACTTTTGGT | 7468 |
rs568050731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927546 | CACATGGTGAAACCC[C/G]CATCTCTACTAAAAA | 7468 |
rs568069325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961306 | TCTTCTGAGGTGCAG[C/T]GTGTCTTTCAGCTGC | 7468 |
rs568069748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976141 | ACCCTGGGTGGCGGG[C/T]GGGAGCTGTTCTGCC | 7468 |
rs568084338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927958 | GCAGTGGTGCAATCA[A/T]AGGTCACTGCAGCCC | 7468 |
rs568094064 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928072 | TTAAAAATAATTTCT[-/T]TTTTTTTTTTTTTTC | 7468 |
rs568159944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933603 | GTTTCACTCTGTTAG[C/T]CAGGATGGTCTCGAT | 7468 |
rs568163817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933010 | CCTATGCTTGGCAGT[C/G]CCTGAGCAGGTCCTG | 7468 |
rs568171973 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940257 | AAGATTTCTTTGTTC[G/T]CATGCATTTCATGGC | 7468 |
rs568200764 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910082 | TCATAAGCTACAGCT[C/T]AATCTAGATTCTTTT | 7468 |
rs568228141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900584 | CCTAGGTTTTAAATG[C/T]AATTGCTTTTTCTTT | 7468 |
rs568233981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895916 | GCTGGCTGGTAGAGG[G/T]GCTCAGGTGATGATG | 7468 |
rs568245764 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968327 | GATGATGATGACTGC[A/G]AGGCAGGAAGGAAGA | 7468 |
rs568308617 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934356 | CCCAAAGTATTGGGA[-/T]TTACAGGCATGAGCC | 7468 |
rs568326800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907875 | CTTGGCCTCCCAATG[A/G]GATTACAGGCATGAG | 7468 |
rs568411907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931949 | CCTCGAAGTGTAAGC[A/G]TAAATTTGATTGTGT | 7468 |
rs568424327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938039 | ACCTCTTGAATGGAA[C/G]GATCCATTTTTCTCA | 7468 |
rs568442055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906950 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCTCATC | 7468 |
rs568442181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915206 | CTGCAAGCTCCGCCT[C/T]CTGGGTTCACACCAT | 7468 |
rs568485747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920369 | GCAGGAGAATCACTT[C/G]AACCGGGAGGCCACA | 7468 |
rs568497507 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979343 | GCGCCGTCGCCACTC[A/G]GGAGAGGCTGGGTGA | 7468 |
rs568514030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882105 | AGATTGAGTTGGTGC[C/T]GGGGAAGGTTCCGGA | 7468 |
rs568563857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926552 | CACAGCTCACTGCAA[C/T]CTCCGCCTTCCGGGT | 7468 |
rs568580622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882688 | CAACAACAACAACAA[C/T]AAAAAACTGGGTTGA | 7468 |
rs568583386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895378 | TATATTTGAAAGAAT[A/G]AAACATTCATGAATG | 7468 |
rs568583435 | snp | A/C | 6.59859e-05 | 0.00574357 | missense | WHSC1 | GRCh38.p7 | 4:1901135 | GAAAATGGACAAAAA[A/C]CAGAAAACAAGGCGA | 7468 |
rs568597524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925820 | TTTGTTTTTGTTTTT[C/G]AGACAGGGTCTTACT | 7468 |
rs568621047 | snp | A/G | 0.000309719 | 0.0124404 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974652 | CGCTCACTAAGGCTC[A/G]GTCCTCTCCACGTGG | 7468 |
rs568622316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889090 | TTTAGTAGAGACGAG[G/T]TTTCGCCATTTTGGC | 7468 |
rs568654631 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914608 | TGGGATTACAGGCGT[C/G]AGCCACTGTGCCTGG | 7468 |
rs568659914 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883408 | AGGCTGAGGCAAGCA[G/T]ATCACTTGAGGCCAG | 7468 |
rs568683192 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888378 | AGATCAGGCCACTGC[A/C]CTCCAGCCTGGGTGA | 7468 |
rs568684570 | in-del | -/AAAA | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966657 | GCAAGACTCTGTCTC[-/AAAA]AAAAAAAAAAAAAGA | 7468 |
rs568719946 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976045 | TGTCTGTCCTCAGCC[A/G]TGTTGCTGAGGATGG | 7468 |
rs568771514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889334 | GAGTAGCTGGGACTA[C/T]AGGCATGCGCTTCCA | 7468 |
rs568796890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894250 | GTGTGAGCCACCACG[C/G]CTGGTGAAGATTTTC | 7468 |
rs568817758 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910505 | GATATTACACTCACT[G/T]GTCTCTTTAGGTAAC | 7468 |
rs568819749 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950605 | CGGCAGCTGGACTGC[A/G]CGGTCACCTGATGAG | 7468 |
rs568834373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1890119 | CTTTCACTTAGCATC[A/C]TGTTTATCTATGTTG | 7468 |
rs568849813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975636 | CCTCACAGACGCGTG[A/G]TTTCGCAGTTCTGGG | 7468 |
rs568853553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932577 | CATGGAGAAACCCCA[C/T]CTCTACTAAAAATAC | 7468 |
rs568858629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875668 | AGCACTTTGGGAGGC[C/T]GAGGCGGTTGGATCA | 7468 |
rs568866933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932925 | TGGCTTTGTGCTCAC[A/G]AACGGGTGTTCTGAA | 7468 |
rs568870713 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875172 | GCAGTGTTTGGGCTG[G/T]TCTCTGTAACTCCTG | 7468 |
rs568872523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968264 | ACAGACAAGTTTGTG[C/G]GTATGTGGATATGTC | 7468 |
rs568932830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967685 | CTAGGTCTGCTTTCT[C/T]GCTGCAGGGAAAGCC | 7468 |
rs568967505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939492 | AGTTTGTCTGCTTTT[A/G]TTTATGTTCAGATTT | 7468 |
rs568981530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938931 | CTAACAGTAAGGGCT[C/T]GTTATTTATATTTCA | 7468 |
rs568982578 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925827 | TTGTTTTTGAGACAG[A/G]GTCTTACTCTGTCGC | 7468 |
rs568985522 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947715 | GGTACTTCTCGCCAT[C/G]AGCTTCCTTCTTTAC | 7468 |
rs568999109 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922470 | TCAAGCTTCTGAAGT[C/T]GTCAATTCTCCCTTT | 7468 |
rs569014037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906289 | CATCACCCAAACTGG[A/G]GTGCAGTGGCGCAGT | 7468 |
rs569045321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881465 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 7468 |
rs569047093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946838 | GTCTCTCCAACAGCC[C/T]GACAGGCCTCATCTT | 7468 |
rs569077048 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913853 | CTTTATTTCTACCAT[C/T]TCTCGTCTCCACACA | 7468 |
rs569078569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906899 | CCTCTGACCTCAAGT[A/G]ATCTGCCCACCTCGG | 7468 |
rs569089149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914545 | TGGCCAGGCTGGTCT[C/T]GAACTCTTGATCTGA | 7468 |
rs569118127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960155 | AGAGCCTCTGTGCCT[G/T]ACCTGAAATATTTTT | 7468 |
rs569119546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954125 | CAGTAGCTGGGATTA[C/T]AGGCACGTGCCACCA | 7468 |
rs569142778 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928889 | CTTGAAGAGTTGGGA[A/G]TGAGTGGGCTCATGG | 7468 |
rs569162741 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958875 | GAGTGTCTTTCGCCA[C/T]CTCTTCCCTAAGATT | 7468 |
rs569180469 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960875 | GATATGTCTGAGATC[C/G]TTTGAATTTAATTTA | 7468 |
rs569192717 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920860 | GCAACATGAAACCCT[C/G]TCTCTAAAAAAAAAA | 7468 |
rs569219597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945124 | TCTCCGAGAGGTCCC[C/T]GCAGCTCTAGGGAGA | 7468 |
rs569244997 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982150 | AAAGCTGTGTTTGGA[A/C]AATTGTGTATGAGTA | 7468 |
rs569248816 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877353 | TGTCCCCAGTCTTCA[-/G]GGGGTGACTCTCACT | 7468 |
rs569257565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881999 | CAGGCAAGTTCTTTT[A/G]GGTCCTGTTAAGAGC | 7468 |
rs569281992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902192 | AGCTGTTTAGTTCTC[A/G]CTCATGTAATGGCAG | 7468 |
rs569282610 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915330 | CGTGTTAGCCAGGAT[A/G]GTCTCGATTTCCTGA | 7468 |
rs569329911 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964068 | TAGAAGGTGACCCTC[A/G]TGAGCAGACCTTCCT | 7468 |
rs569330055 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879433 | ACCGTGTTAGCCAGG[A/T]TGGTCTCAATCTCCT | 7468 |
rs569331423 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925778 | TATATATATATTTTT[G/T]TTTGTTTGTTTGTTT | 7468 |
rs569354947 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931891 | TAAATGACTGGCTTA[C/T]TTAAAAATGAGCCAG | 7468 |
rs569362443 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893552 | TTTTTTGTTTTTTTT[G/T]TTTTTTTGTTTTGTT | 7468 |
rs569368414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978564 | CTGACAGTTGTAAGT[C/T]ATCTTCAACCACGAT | 7468 |
rs569369695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888204 | GATCACCTGAGGTCA[A/G]GAGTTCGAGACCAGC | 7468 |
rs569374683 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982186 | GTATTAAAAACATTT[G/T]AAAGGCTTTTTTCTT | 7468 |
rs569382422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931272 | TTGCCTGAGAGCTCA[C/T]AGGGCAAGAAGGGTG | 7468 |
rs569412351 | snp | A/C/T | 4.51949e-05 | 0.0047535 | missense | WHSC1 | GRCh38.p7 | 4:1978863 | GGAAGCCGAAGGGGA[A/C/T]GAGGCGGCGGCGGAG | 7468 |
rs569446001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937403 | AATCATACTGAAACT[A/G]GTTGTTTTGAAATAT | 7468 |
rs569456866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906927 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 7468 |
rs569457736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886099 | AAACTAAAGCGCGTC[C/T]ATTGAAGACGTATGC | 7468 |
rs569469353 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937841 | TTTCAGAATCTCAGC[C/G]CTTGAGAAAAGCTTC | 7468 |
rs569508489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971094 | CCGGGTGCAGTGGCT[A/C]ATGCCAGTAATCCCA | 7468 |
rs569524898 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908447 | TGATAATATACTTTT[G/T]TGTGTGTGTGAAGGC | 7468 |
rs569537917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971742 | CAGTTCCTTGTGACC[A/G]AGTGGGGTTTACCCC | 7468 |
rs569541901 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936747 | TTCATCCTGTTTTTC[A/G]CTGATCTGAGTTAAA | 7468 |
rs569542496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899280 | CCCCCTATTGCTGCA[C/T]GTCAGGTGTCCTCCA | 7468 |
rs569574937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879097 | TCTGGAGCTTCACTG[C/T]TTGCTTAGAAGAGAA | 7468 |
rs569612459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910052 | GTATAATATACATGC[A/G]AAAGTGAACATAACT | 7468 |
rs569616463 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883514 | GCGCACACCTGTAAC[C/T]CCAGCTACTCAGGAG | 7468 |
rs569618048 | snp | A/G | | | missense | WHSC1 | GRCh38.p7 | 4:1918218 | AGAAGCTGCAAGCAT[A/G]TCAGTGGAGGAGCGG | 7468 |
rs569648109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917887 | CCCAGTTCAAGTGAT[C/T]CTCATGTCTCAGCCT | 7468 |
rs569667227 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876572 | TGGTGTGTGCCTATA[A/G]TCCCAGATACTTGGG | 7468 |
rs569671675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929604 | TGGGCAGCATGGGAA[C/G]AAATGCATGGGGCTG | 7468 |
rs569685689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885304 | AGTAAAGGGCAGAAA[C/G]AAGACATTGCCAGTG | 7468 |
rs569689488 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940495 | AAATAGCCACAGAAC[A/G]TAGGTGTGACACTTT | 7468 |
rs569689868 | in-del | -/T/TTAT | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946258 | TCTTGCATTTATTTA[-/T/TTAT]TTATTTATTTATTTA | 7468 |
rs569739705 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973852 | TGATTTCTCCCCACG[-/C]GGTTGTGCGGTGGAT | 7468 |
rs569788506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922799 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 7468 |
rs569797447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948664 | CAGGAAATGAGCCTC[A/G]TGTGTGTCGTTAACA | 7468 |
rs569831013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884951 | CTGTCTCTACTAAAA[A/G]TACTAAAAATTAGCC | 7468 |
rs569851245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976764 | GCTCTTCCTGCTGAC[C/T]GGGCCTCATCTGGGT | 7468 |
rs569865607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928806 | TGAGGAGGTGAGAGG[C/T]AGATGTGTTGTGGAT | 7468 |
rs569876650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891358 | CATTTCAGTCTTTTC[C/T]GCCCCCGGAGGAATG | 7468 |
rs569937654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897035 | GCTGGGCATGGTGGC[A/T]AGTGCCTTGTAGTCC | 7468 |
rs570033446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956470 | CAGAAATGTTCCATG[C/G]CTTGCCTTTATGTAA | 7468 |
rs570071366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878330 | CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAAGT | 7468 |
rs570101942 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908603 | CAGAACAAAGAGAAG[A/T]GAGGGAAGGACAGAG | 7468 |
rs570121331 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938160 | GTCTTGGCGTGGCCC[C/T]ACCCACCTCGCCCTC | 7468 |
rs570132024 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877770 | TTCCTTCTTTGACCT[C/G]GAATGCTGTCCCCAG | 7468 |
rs570179258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884050 | ATGAAAACTTACAAA[A/G]TGAGACTACTGAGAA | 7468 |
rs570203245 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978396 | CTCCTCTCAGTTGCC[A/G]AAACATAAAGAGACG | 7468 |
rs570210134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927882 | TTTCCATGTTTTTTT[A/G]GTATGTTTTAAATTT | 7468 |
rs570238061 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943292 | TTGGCTGTGTTTTAT[C/T]TTTAATGAACGTTTC | 7468 |
rs570243966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884222 | CACCTCAGCCTCCCA[A/G]GTAGCTGGGACTATG | 7468 |
rs570255560 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880368 | CTTTGTTTTGCCTCT[C/T]GGAAAACTAACATAC | 7468 |
rs570285988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876874 | CGGTGGGTGGCTCAC[A/G]CCTGTAATCCCAGTG | 7468 |
rs570288174 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981299 | AGGCTTTGGGGTAGC[A/G]GCCCTGAGCTTGCAG | 7468 |
rs570290544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976174 | TGGTGGCCTCCTTTG[C/T]CAGTGGGTCCCATCA | 7468 |
rs570327697 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980939 | AGGCCGGGCAGTGTC[C/T]CCACACACACCTTAG | 7468 |
rs570336851 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909520 | GACAGTGAGTGGTGA[A/G]TGTCGTTGTTTTGGA | 7468 |
rs570346572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927460 | CAGTGCCTCATGCCT[G/T]TAATCCCAGCACTTT | 7468 |
rs570389485 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963252 | CGCCTCTAGGACCAT[C/G]GCGTGTAGAGCAGGC | 7468 |
rs570396559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969131 | GGGCCTGCCCCCAGC[A/G]GCGCTGAGAGTTGAA | 7468 |
rs570404268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976037 | TGAGCCGGTGTCTGT[C/T]CTCAGCCGTGTTGCT | 7468 |
rs570450428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970902 | GTGAAAGGCTGAAAG[C/T]CCATAGAAACAAGCA | 7468 |
rs570459575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934423 | CTGGGCTATCAGGAG[G/T]CAGAGGTTGCAGTGA | 7468 |
rs570465911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955590 | TGTTTTAAAACTGAT[C/G]TTTATAAGTTAAGGC | 7468 |
rs570465983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947928 | AGAAGGTGGCATCTG[A/G]CTGCGGCTCATACAG | 7468 |
rs570567378 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928086 | CTTTTTTTTTTTTTT[C/T]CAAACACGATCTTTC | 7468 |
rs570591749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933645 | GTGATCCACCCACCT[C/T]GGCCTCCCAGAGTGC | 7468 |
rs570620419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890786 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 7468 |
rs570636897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896323 | TGCAGCCTATGAGGC[C/T]CCAGACTGCTGTTCC | 7468 |
rs570695212 | snp | A/C | 1.65277e-05 | 0.00287464 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939665 | ACAGCAACGAAAAAT[A/C]TGTCTGATGCATGTA | 7468 |
rs570801318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926565 | AACCTCCGCCTTCCG[A/G]GTTCAAGCGATCCTC | 7468 |
rs570845362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901643 | GATGTGGTCAGTGGA[G/T]ACAGGCTGGGCTCTA | 7468 |
rs570878239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914797 | CTTCACATACCTTGC[A/T]ATTCTATTTCTTGTT | 7468 |
rs570884841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915274 | GCGCCCACCACCATG[C/G]CTGGCTAATTTTTGT | 7468 |
rs570919533 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908128 | TTGAGATGCATACTC[A/G]GCATCTGGTGGTTGT | 7468 |
rs570933509 | snp | C/T | 0.000104348 | 0.00722241 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955370 | GGTGTCTGCGGCACA[C/T]GCCTCTCACACTCCC | 7468 |
rs570938166 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972994 | AGTAACTGGGATTAC[C/T]GGTGCCCACCACCAT | 7468 |
rs570991456 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947811 | ATTGTATTTCAAAAA[C/T]GATGTCGTATTCAAG | 7468 |
rs571012494 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969090 | GAGACACGGGAGTGC[A/G]GCCTGGCAGGCAGAG | 7468 |
rs571037527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973448 | CAACGTGCACATCAG[C/T]ACCGCGGCTCAGCGC | 7468 |
rs571076730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882911 | TGATTCTGATGCCCT[C/T]GAGTTGAGAGCTACT | 7468 |
rs571082337 | in-del | -/C | 0.00319042 | 0.0398125 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924755 | ATCTCTACAAAAAAA[-/C]AAAACAAAACAAAAC | 7468 |
rs571085182 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943763 | TAAAGATGGGGAAAA[A/G]AAGATGGTATAAAAA | 7468 |
rs571124361 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933750 | AACCCCTCCGTAAAG[C/T]AGTCATGCAAATGAT | 7468 |
rs571138999 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924740 | ACACAGTGAGACTCT[C/G]ATCTCTACAAAAAAA | 7468 |
rs571156923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889143 | CCTCAGGTGATCCAC[C/T]CGCTTTGGCCTCCCA | 7468 |
rs571191436 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981342 | CTGGGGCTGACCACG[C/T]CCCCAGCTGTGACCG | 7468 |
rs571199840 | snp | C/T | 1.72282e-05 | 0.00293492 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974744 | GGACACAGGACACCA[C/T]GGTTTTCAGTACAAC | 7468 |
rs571211280 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911717 | CAGTGAGATATTCAC[C/T]TCTCAACTTGGACCA | 7468 |
rs571214455 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930133 | CGTGTGCTGGCCTGG[G/T]CTGTGACAGAAGCCA | 7468 |
rs571225808 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937213 | CGTGCCACCATGTCC[A/C]GCTAATTTTTTTGTA | 7468 |
rs571245728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898669 | CGTCTAAAAAAAAAA[A/C]AACAAAAAACAAAAA | 7468 |
rs571266971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912461 | TTCTTGTAAAACCTT[C/T]TGTTTCCCTTGGAAT | 7468 |
rs571275268 | snp | A/G | 2.21668e-05 | 0.0033291 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918682 | GAGGAACATCCCTTC[A/G]GTGCAGAATCATCTG | 7468 |
rs571275771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929723 | CAGAAACAGGTGGTG[A/G]GTTACACCTGGCTGG | 7468 |
rs571290498 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896718 | TTCCTCTCCTTCCTT[C/T]CTTTCCTTCCTTCCC | 7468 |
rs571304238 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958651 | CCGGAGGTCAGGTGC[G/T]CTGCCTTTGCTTGTA | 7468 |
rs571307249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959217 | CTCTTGTTCATCAGC[A/G]ATGTGCACAGACACT | 7468 |
rs571307698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904858 | ATGTACGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 7468 |
rs571321221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898383 | TAAAAATGGTTTCGT[A/G]GCCAGGTGCGGTGGC | 7468 |
rs571336211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964053 | GTTTACAAAGCGCAA[C/T]AGAAGGTGACCCTCG | 7468 |
rs571338769 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911135 | AGAGTCACAAACTAC[C/T]TGTAGTCTAATGGGC | 7468 |
rs571376296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897729 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 7468 |
rs571382117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904100 | GCAAGGGAGCACACT[C/G]CATTTTTGGGGGTCT | 7468 |
rs571382666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958090 | TCTTCCCCGAGGGCC[C/G]TGAGAGGTTCTTAGG | 7468 |
rs571411142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873499 | GCTTTCAAACCAGTA[C/T]TTGCTGAAGTGTGCG | 7468 |
rs571426190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880655 | CAGTCAAGCTCCTAT[A/G]TTTAACAACCAATCT | 7468 |
rs571439420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886266 | GGCTGGAGTGTGGTG[A/G]TATGATCTCAGTTCA | 7468 |
rs571441557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964949 | CAATCAAAACAAGAA[C/G]AATAAATAAAAATAA | 7468 |
rs571448644 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893788 | GAGCTCAAGCGATCT[A/G]CCTGCCTCGTCCTCC | 7468 |
rs571468619 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898492 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7468 |
rs571483099 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885833 | AGGACAAGTTCCAGG[C/T]GCAGGAATGATATAG | 7468 |
rs571487579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1880163 | TCCAAAATTCGGAGT[C/T]GGTGTAATCTTTGTA | 7468 |
rs571490270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903806 | GTGGCGTGATCTCGG[C/T]TCACTGCAAGCTCCG | 7468 |
rs571511285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930547 | GTTCTAAAGGGCCGT[A/G]CATTTGATTTCATGC | 7468 |
rs571546073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892224 | CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCCTTGG | 7468 |
rs571559498 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903149 | GCATGCTTATGGCAA[-/T]GGTTTTGGGCCGGCC | 7468 |
rs571598393 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938853 | TCAGGTTTCTTACTT[C/G]ATGGTGCCAGTTGCT | 7468 |
rs571603879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972094 | TCTCGGAGAATGTGA[C/T]GGCTGTGTTTGGTGA | 7468 |
rs571609863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885473 | AAGTTGATAAAACTT[C/G]TGATATGTTGATAAA | 7468 |
rs571622003 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891836 | CACTCCAGCCTGGGC[A/G]ACAGAGGGAGACTCC | 7468 |
rs571629440 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943395 | CCGTGGTTTCCTGTT[G/T]TGACAGTAATAATGG | 7468 |
rs571649417 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882539 | CGTGGTGGCGGGCGC[C/T]TGTAGTCCCAGCTAC | 7468 |
rs571652928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878936 | AGGGTCCTTGGTCCA[A/G]TCCTTACAGATGGAA | 7468 |
rs571657178 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879966 | GGTTGTGAATTTTTC[A/T]AGGTGAGGGCCCTTT | 7468 |
rs571666836 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982069 | AAATTCACTTTTTGG[A/G]GGGAGGGATATACTG | 7468 |
rs571693539 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935226 | TGAGGACACACCCAG[A/G]AAAAGACTCAGGACG | 7468 |
rs571723898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942557 | CAGATAACAAATTTT[A/G]AGACCAAGGTAAGAT | 7468 |
rs571793696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909958 | TTAAAAAAAAAAAAA[A/G]TTATTTATCATGCTT | 7468 |
rs571830219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1871724 | CAGGGGCTGGGGGAC[C/T]GGGAGGCCGGGCGGC | 7468 |
rs571841363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1950053 | GGAAATGTAGTTTAT[A/G]CTTTTGCTCTGTTTC | 7468 |
rs571903273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943094 | GCATCAGTTGCTTCT[A/G]TAGAGCATCAGCCCT | 7468 |
rs571910558 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963522 | TCTAAATGTAAACTA[C/G]TTATGTGCTGTAAGA | 7468 |
rs571952166 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870394 | GGTGTTCCCGGCTCC[C/T]TGAACCTGCGTGACA | 7468 |
rs571956901 | snp | C/G | 0.030278 | 0.119257 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957377 | CAACCTCCACCTCCT[C/G]GGTTCAAGCAATTCT | 7468 |
rs571960610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950444 | TGGGGAGAACAAGTG[A/G]ACTGTGAAATATCAG | 7468 |
rs571972104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962824 | TACAGGAACATGCCA[C/T]CACACCTGGCTGATG | 7468 |
rs572018365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956785 | CCGAGGTGTGTGCAT[A/G]TGGCTCGTTCAGGGA | 7468 |
rs572056027 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897491 | GAGACCCTGTCTCAA[A/G]GGAAAAAAAAAATTG | 7468 |
rs572074163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928472 | GTGTTTTTAGAACTC[A/G]TAACCATCATACCAT | 7468 |
rs572100999 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870571 | CTCCTCCTCCCTGTG[C/T]CGCACGCAGTCGCCC | 7468 |
rs572118572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903924 | TATTTTTAGTAGAGA[C/T]AGGGTTTCATTGTGT | 7468 |
rs572131540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949727 | TGAGATTGTACCACT[A/G]CACTCCAGCCTGGGC | 7468 |
rs572133123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910160 | TAGCATTGTTGTAAT[C/T]TACAGCAGCAGAACC | 7468 |
rs572164850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878515 | AATTCCTGGCTGCAT[C/T]GGGTCATCTGTGAAG | 7468 |
rs572182957 | snp | A/G | 3.49351e-05 | 0.00417927 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917060 | ATGACCCTTCAGTCT[A/G]CTTTTAGACCAGAAA | 7468 |
rs572196207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909323 | TTCTTTGAGTACAGA[A/G]TAGTATGTAGGAGCC | 7468 |
rs572211378 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971197 | GACCCTGTCTCAATT[A/T]AAAAAAAATTGTGGC | 7468 |
rs572223351 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870083 | TCTTGCAGCAACCCT[G/T]GTTTTTTTGGGGGGG | 7468 |
rs572236192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922957 | CAGTATTCACGCAGG[A/G]CAGTGATATGGCCCA | 7468 |
rs572348126 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976841 | GCAGAGCCTTTCTTT[C/G]TTCCACCAGCCGCAC | 7468 |
rs572350121 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880742 | AATGTGGGAAACTAT[A/G]AGACCAGTAAGCCAT | 7468 |
rs572365346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908020 | CGCATTTCGGGAAAC[A/G]TCACATCAGTAACAA | 7468 |
rs572381643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1970508 | GCAGTGGCAGCTGCC[A/G]GGGGTGAGTGTGCCA | 7468 |
rs572398513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884990 | TGGCGGCAACCTGTA[A/G]TCTCAGCTACTCAGG | 7468 |
rs572428984 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907340 | CATGTTTGACCAGTT[A/T]TTAACCCTGCAGCCA | 7468 |
rs572431113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915396 | TGGGATTACAGGCTT[C/G]AGCCACTGCACCCGG | 7468 |
rs572439604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976259 | GCTTCCGACAAAGCT[C/T]ACTCTAGTCGTAGTC | 7468 |
rs572441287 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970457 | ATGAGCTCCAGGCCT[C/G]CAGCAGAATCAGGTG | 7468 |
rs572442971 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926968 | ACAGTTTCTGTGGGC[C/T]AGGAATTTGGCAACC | 7468 |
rs572462178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1884318 | CCAGGCTGGTCTCGA[A/G]CTGCTGAGCTCAAGT | 7468 |
rs572472570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925549 | GACCACAGGCACATG[C/T]CACCACATCCGGCTA | 7468 |
rs572474424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890958 | GAGTGCAGTGGCGTG[A/G]TCTTGGCTCACTGCA | 7468 |
rs572485032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940670 | AGATGATAACTGGGG[A/G]CCCTTTTGGAACAGG | 7468 |
rs572524015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902298 | GGTGTGATCATGGCT[C/T]ACAACAGCCTTGACC | 7468 |
rs572539076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890580 | TGCTGGGATTACAGG[C/T]GTGAGTCACCGCACC | 7468 |
rs572540578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874886 | AATGGTTATTTACAG[C/T]GAGTACTTTGGGGGA | 7468 |
rs572551382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939949 | TGAAATGGACAAACA[A/G]TGCACTATGTTAGTT | 7468 |
rs572577730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1896144 | GACAGCAGCTCCACA[C/G]TTGGTGCTCCTAATC | 7468 |
rs572584004 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980633 | CCTGCAGGGTCCCAC[A/G]CCTCCCTGAGCACTG | 7468 |
rs572584648 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931524 | GTATCAATTTAAAAT[A/T]AAAAAAAAAAGTACT | 7468 |
rs572639628 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901792 | TCCAGCAGATGGCCT[G/T]CCTCCCTGAGGCCTA | 7468 |
rs572644611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931069 | GCTGTGTGAAGAGAG[C/G]ACACAAGAAGGAAGG | 7468 |
rs572806303 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889681 | TAATTTTGTATTTTT[A/G]GTAGAGAGAGTTTCA | 7468 |
rs572824457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904454 | CCAGGCTTCTTTCTT[A/G]CTCTTTCTAAATAGC | 7468 |
rs572827873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959136 | CTGGACACCCTGCAG[C/T]GTACTAAGCAATCAA | 7468 |
rs572852405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973993 | GTTCTAGGCCACATC[A/G]TGCTTGCATTTGTGA | 7468 |
rs572870720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881626 | GGTCTTGAATTCCTC[A/G]ACTCAAGCAGTCCTT | 7468 |
rs572885119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887813 | TTGGCTTTATTTTCC[A/G]TGTATCTGTTACTAA | 7468 |
rs572904619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937088 | AGGGAGTCTCACTTC[A/G]TCACCCAGGCTGGAG | 7468 |
rs572917650 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961861 | GCTGGGGAAGTGTGG[C/T]CTCCTTAGTGCCTGA | 7468 |
rs572936745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911386 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 7468 |
rs572937079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1937567 | CTTGTCTCTTCAGAT[C/T]TGGGTTTTATAAACC | 7468 |
rs572943975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886739 | GCTACTCAGGAGGCT[A/G]AGGCAGGGTACTCGC | 7468 |
rs572980332 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940123 | TGGAAGTAAGTCTGC[A/G]TTGGTTCTGAAAGGG | 7468 |
rs573065823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978371 | GGGGACACTCCTGCA[A/C]CCGGCACAGCTCCTC | 7468 |
rs573080771 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904986 | AAATACAAAATTAGC[C/T]GGACGTGGTGGTGCA | 7468 |
rs573082112 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892089 | TTTGTTTGTTGCTCT[A/T]TTTCCAAGTGCTGGA | 7468 |
rs573118784 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883914 | GGTTTTCTACACAGT[A/T]GCCTAGGATAGAGGC | 7468 |
rs573143623 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890772 | CTTGGCTAATTTTCT[A/G]TTTTTAGTAGAGACG | 7468 |
rs573148109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873653 | GATTATCTTCTCCTT[A/C]TAAAAGTAATCAAAT | 7468 |
rs573151735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977394 | AGGGTGCAGCCACCT[C/T]CGTTACAATCTTGCA | 7468 |
rs573174416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873051 | CAAATCTAAACTGCC[A/G]AATGGAGATGAAGAG | 7468 |
rs573191011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966323 | TGTATTGTTGTAACC[A/G]TGGTTTATAACTCCA | 7468 |
rs573224031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918897 | TCATGCCTGTAATTT[C/G]AGTACTTTGGGAGGC | 7468 |
rs573275647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958211 | TGGCATGGGGGGATC[C/T]GCATGGGGGTTCTTG | 7468 |
rs573278860 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912594 | AAGTTAGTTTCTCCT[A/G]TTTATATATTTATAT | 7468 |
rs573397474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971850 | AAAATCATTTGAGAA[A/C]ATTCAAACCTATTCC | 7468 |
rs573401362 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881596 | GAGACAGGGTTTTGC[C/G]ATGTTGCCCAGGCTG | 7468 |
rs573429057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891878 | AAAAAAAAACAAAAA[A/C]AAACAAACAAAAACG | 7468 |
rs573441816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936106 | CAGCATAGATACAAA[A/G]CCAGCCCCGGGTCCT | 7468 |
rs573442129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930354 | TTTGGAAAAGTATAT[A/G]TATATTTTTATCATT | 7468 |
rs573453906 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943820 | CAAAGTAAAGACTCT[A/C]TCTTGAAAGGCTTTT | 7468 |
rs573552860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911322 | GCCAGGTGCAGTGGC[A/T]CATGCCTATAATCCC | 7468 |
rs573553928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973135 | TAGGTGTGAGCCACC[A/G]CGCCCGGCCGACATA | 7468 |
rs573558480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935921 | TAGGGCTTATTATTC[A/G]GGATGTAAGTAATGA | 7468 |
rs573591581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978343 | GCAGCCCCTGCCTGT[C/T]CACGCCGCGCTGGGG | 7468 |
rs573643575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898770 | TGGAATCAGCCTGGA[A/C]TTTGGGCAGAGTTTA | 7468 |
rs573648299 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926279 | CCTGACTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 7468 |
rs573696906 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953793 | TTTGTTTACCCTGGC[-/T]TTTTTTTTTTTTCTT | 7468 |
rs573722870 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917609 | GCCTGGCTAATTTTT[G/T]TATTTTTAGTGGAGA | 7468 |
rs573755986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904936 | AGGAGTTCGAGACTA[A/G]CCTGACCAACATGGT | 7468 |
rs573814536 | snp | A/C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923260 | TTGGGAGGCTGAAGC[A/C/G]GGAGGATTGCTTGAG | 7468 |
rs573885483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891868 | TCTCAAAAAAAAAAA[A/C]AAACAAAAAAAAACA | 7468 |
rs573900990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876766 | ATGCTTTTTTTTTCT[A/G]GAAGGAATTGGAACC | 7468 |
rs573963417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897378 | TAGTCCCAGCTACTC[G/T]GGAGGCTGAGATGGG | 7468 |
rs573966425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879388 | CATGCCCGGCTAATT[C/T]TTTTGTATTTTTAGT | 7468 |
rs573971978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957628 | GAGAACAGCAAGTCC[C/T]AGGCTTTGACCCTGG | 7468 |
rs574015244 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924218 | TAATCAGCAATGTGT[G/T]TACAGCCACCGTTTC | 7468 |
rs574016629 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889810 | TGTGCCCAGCCGACC[-/T]TTTTTTTTTTTTAAT | 7468 |
rs574022657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872960 | CGCCAACAACATAAA[A/G]CAAACAAGTTCTGTG | 7468 |
rs574034563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872291 | CGCCCCAGGATGCAG[A/G]TTGATAGTCCTTGAA | 7468 |
rs574063775 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929759 | ATTAGTGTGTCAGCC[C/T]TGTGCCCTGCTCTCG | 7468 |
rs574076246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1885527 | TCTCAGTGGCCCCTG[C/T]TGACATGTATTTTGA | 7468 |
rs574087324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964545 | GGTGAGCAAGAAGGA[A/T]CCTTTTCTCCAAATA | 7468 |
rs574087647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972278 | CAAGAGATGATATGG[A/G]TGAGTGGCGGTACAG | 7468 |
rs574100776 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887227 | AGGCTGCTTGGGCTT[C/T]CTTGCAGCGTGGTGG | 7468 |
rs574133276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914983 | AAGCCTATTATTTGG[A/G]TATCAAACCTCCTAG | 7468 |
rs574148489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1971732 | GCATGGAGAGCAGTT[C/G]CTTGTGACCGAGTGG | 7468 |
rs574148650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977334 | GTCTGAGAAATGGGT[C/T]GTGAGATGACTCTGG | 7468 |
rs574151436 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929138 | GGGCATTGGTGGGTG[G/T]TGGTGTCCAGGCCAG | 7468 |
rs574185810 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982143 | AAAATGGAAAGCTGT[C/G]TTTGGAAAATTGTGT | 7468 |
rs574210284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976905 | GTGGTGACGGGGTAG[C/T]CCCTGGAACCTCCAG | 7468 |
rs574258495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935317 | TGCTCTGTGACTCTT[A/G]GTGCCACTGTTTCCC | 7468 |
rs574263193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916665 | TTTCTTTCCCATTCA[A/G]TTTTGAACCTTATCT | 7468 |
rs574326156 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981631 | AGAACCCAGCTGTCC[A/G]TCCTCAGGCCGGCCT | 7468 |
rs574326272 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979564 | GTTTTTTCTCCTCAT[C/G]GATTTGAATGAAATG | 7468 |
rs574372820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934735 | TGCCTGTAATCCCAG[A/C]TACTCAGGAGGCTGA | 7468 |
rs574373817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921713 | GTTGAACCTGGGAGA[C/T]GGAGGTTGCAGCGAG | 7468 |
rs574387690 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949373 | GTTTTCTTTAGACTT[C/T]GTGCTGTCAGGAGAT | 7468 |
rs574389171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1876165 | CTTGCAGTGAGCTGA[C/G]ATCGCGCCACTGCCC | 7468 |
rs574462687 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921246 | GTAGATCACTTGAGG[G/T]CAGGAATTCAAGACC | 7468 |
rs574505939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883178 | TGCCATTTACTGTCC[A/G]GATAGCATTCTTTCT | 7468 |
rs574510563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926344 | ATTTTTAGTAGAGCC[A/G]GGGTTTCACCATGTT | 7468 |
rs574537239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882543 | GTGGCGGGCGCCTGT[A/G]GTCCCAGCTACTCGG | 7468 |
rs574547464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895556 | CAATACTTTTTTTTT[C/T]CCAAGTCTGCAAATC | 7468 |
rs574573425 | snp | C/T | 0.00016472 | 0.00907375 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974877 | GGACCGTATAATAGA[C/T]GCTGGCCCCAAAGGA | 7468 |
rs574684646 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959695 | CAAGATCATCAAGAC[A/T]GATGGCAAAGGGTGG | 7468 |
rs574695192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967353 | GGGAGGCCGAGGCCG[A/G]CAGATCACAAGGTCA | 7468 |
rs574716246 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905117 | TCTGGGCAACAACAG[C/T]GAAACTCTGTCTCAC | 7468 |
rs574730827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946273 | ATTATTTATTTATTT[A/T]TTTATTTAGAGACAG | 7468 |
rs574747890 | in-del | -/A/AT | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939460 | CCAAGTAGCGAGGAC[-/A/AT]ATGGGGTTCATTGTA | 7468 |
rs574748523 | in-del | -/TATT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873852 | TATTTTGTCCTGTGC[-/TATT]TATTTATTTTTAGAG | 7468 |
rs574758473 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966589 | GTGAACCCGGGAGGC[A/G]GAACTTGCAGTGAGC | 7468 |
rs574758845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945731 | GGGTTGCCTTGGCAG[C/T]AGAGGCTCCTCTGAT | 7468 |
rs574762155 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1932203 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 7468 |
rs574794395 | snp | C/T | 1.65321e-05 | 0.00287502 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953463 | CCGAGGTTTCCGCTG[C/T]CCCCTCCACAGCTGT | 7468 |
rs574928064 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920543 | GATAAAATTCATTGC[G/T]TTTTTTAATTAAGTA | 7468 |
rs574990040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926102 | GCCAGTGCACCTGGC[A/C]GGCTCCAGTATGAGC | 7468 |
rs574999814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913230 | TTGGACTAGCGGTAA[C/T]GCCAGTGCCTGGGAA | 7468 |
rs575004995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925587 | TATTTTTAGTAGAGA[C/T]GGGGTTTCATTATGT | 7468 |
rs575022373 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939454 | TTGGGGGCCAAGTAG[C/T]GAGGACATGGGGTTC | 7468 |
rs575032816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924960 | TTGAGCTCTGTGTTA[A/G]TGTCCAACACTCTGC | 7468 |
rs575081194 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894675 | AGACCCTGTCTCAAT[A/T]AAAAAAAAAAAAAAA | 7468 |
rs575098461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893804 | CCTGCCTCGTCCTCC[C/G]AAAGTGTTGGAATTG | 7468 |
rs575101070 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898530 | TTAGCCGGGCGTGGT[C/G]GTGGGCGCCTGTAGT | 7468 |
rs575101334 | snp | C/T | 0.00202722 | 0.0317726 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938430 | TCTTTTTTTTTTTTT[C/T]TTTTTTTTTTTAAAT | 7468 |
rs575110730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919734 | GTCAGGAATTTGAGA[C/G]TATCCTGGCCAACAT | 7468 |
rs575130605 | snp | C/T | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952469 | CTTTCCATCAGGTGG[C/T]GGGCAGGGTGGCGGG | 7468 |
rs575137846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968771 | TAATGTTTGTAGTTA[C/T]TGGGGTGGAGGAGAC | 7468 |
rs575161737 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899439 | TAAAAAATGCTTCCA[G/T]ATGAGGTTAAGTGTC | 7468 |
rs575188526 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885037 | ATCGCTTGAACCCGG[C/G]AGGCGGAGGTTGCAG | 7468 |
rs575214548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898926 | GTTCCCTTTCTTTCA[A/G]CAGTTGGTTCCGTCC | 7468 |
rs575221541 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959980 | ATCCTCCCACCTTAG[C/T]TTCCCAAGCAGCTGG | 7468 |
rs575228417 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909445 | TTGCTCCAAGTGGAG[C/T]TCTTGGGTCCATTTT | 7468 |
rs575237653 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887475 | CAAAGAATTATTGAC[C/T]ATCTTTATTTATATT | 7468 |
rs575272883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1888644 | ATCTCGGCTTACTGC[A/G]GCCTCCACCTCCAGG | 7468 |
rs575317614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1967976 | TTATCTGGGAAATTT[C/T]AGTTCTTTGATACTA | 7468 |
rs575320347 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931656 | TGGCCACATGTGCCT[A/G/T]CTGTCACCTTTCTCT | 7468 |
rs575335072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1887909 | TGTCAGTTCCTTTTT[C/T]TCTTTTTTTTTTCTT | 7468 |
rs575342871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923481 | TGCGGCCATGCCCAG[A/G]AAGCTGTATGTTACG | 7468 |
rs575365129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938420 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs575369862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873731 | AGATTCAGTGTAAAA[A/C]ATGCAAAAGTAGCTG | 7468 |
rs575432818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873173 | GGCTGATGGTTGGTA[G/T]AGTGAGGACTTACTG | 7468 |
rs575449490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973051 | TAGAGACAGTTTCAC[C/T]ATGTTGGCCAGGCTG | 7468 |
rs575479147 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919761 | ACATGATGAAACCCC[A/G]TCTCTACTAAAAATA | 7468 |
rs575486565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978315 | GAGGGCAGGTCACAT[A/G]GAAATCAGCACAGCA | 7468 |
rs575489058 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917226 | TTAGAGACACAACTG[-/A]TTTTTTTTTGCTCAT | 7468 |
rs575503441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972425 | TCAAAGTCCATGTAG[A/G]AGGAAAGATCTGCAG | 7468 |
rs575503931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973750 | GAAGCCTGCCGCTTC[C/T]TGGGACCATGTTTAT | 7468 |
rs575574826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1905449 | TGGCCCCTTGGTGGT[A/C]CTTGCGTACATGTCC | 7468 |
rs575606482 | snp | A/T | 0.000284051 | 0.0119141 | intron-variant | WHSC1 | GRCh38.p7 | 4:1912046 | TACAAAGTTTTAAAG[A/T]AATGGAAGAAGTCAC | 7468 |
rs575615858 | snp | C/T | 0.000164769 | 0.0090751 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959626 | CCCGCAGGTGTGTCC[C/T]GCGGGCGAGTTCTGC | 7468 |
rs575656476 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870432 | CAAGGCCGCCGGCTC[C/T]GGCAGCACCTGGAGG | 7468 |
rs575661756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889021 | TTCTGCCTCAGCCTC[C/G]CGAATAGCTGGGATT | 7468 |
rs575667440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952927 | GCCCCACAGCAGCAC[C/T]TCACTTATGGGAGTG | 7468 |
rs575675818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911226 | AGGTTCTCTTCGAAG[C/G]GGATGTAGGTGGGGA | 7468 |
rs575682484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958946 | CTTTGTTATTTGGTT[G/T]CTTGTCTTTCACTAA | 7468 |
rs575686817 | in-del | -/GAGA | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945996 | GTATACAGACCAGGT[-/GAGA]GAGAGCCCTTTTGCC | 7468 |
rs575745542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1966394 | GGGCATGGTGGCTCA[C/T]GCCTGTAATTCCAGC | 7468 |
rs575763753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963485 | ACATCGAAGCCCTAG[A/G]TCTGTGCCTTATGTT | 7468 |
rs575764510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919656 | ACAATAGTGTTGGCC[A/G]GGCACAGTGGCTCAC | 7468 |
rs575802266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1965546 | CTCCAGATGATCAAA[C/T]TTTCGAAAACCAGAA | 7468 |
rs575825387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962701 | CTTTTTTGAGACAGG[G/T]TCTCTATCACCCAGG | 7468 |
rs575836238 | in-del | -/TCT | 0.00438332 | 0.0466095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908885 | CCTGGGCTCAGGTCA[-/TCT]TCTTCCTGCCTTGGC | 7468 |
rs575844014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1877272 | CATTTTTCCGACTCC[A/G]GTTTTACTGTCTTCA | 7468 |
rs575857137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930452 | TTTCATTGAGTCACA[A/G]CATCAGTTAAGCACT | 7468 |
rs575867862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893020 | AAACGAGGAATTCTT[A/G]GGTTATTAGTCTTCT | 7468 |
rs575898636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969817 | AGTTATACTCTAATA[A/T]TCACAGATTTTTTGA | 7468 |
rs575927669 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903233 | CATGTGTATAGTGCT[C/G]TTGAGCAAGGCTAGA | 7468 |
rs575928890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1911385 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 7468 |
rs575942740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924913 | GTTTGGATGACAGAG[C/T]GAGACCCTGTCAAAG | 7468 |
rs576003955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924381 | GGAACCGCCCCGTCA[G/T]CCACTCTGGTATGTT | 7468 |
rs576027126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902587 | TGCTTGGGAAGAGGC[C/T]TGTGCAAGTTGTCAG | 7468 |
rs576109965 | in-del | -/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942041 | ATGTTTGTATTTCCT[-/C]CCTTTCATCACATTT | 7468 |
rs576110583 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976919 | CCCCTGGAACCTCCA[-/G]GGAGGGATTCAGGCA | 7468 |
rs576114551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939872 | CTCAGACTTCATAAG[C/T]GCAGCATTGGTGCTC | 7468 |
rs576117070 | snp | A/G | 9.9734e-05 | 0.00706095 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955950 | CGCTGTCTCTGAGGA[A/G]TCTGTGAATCCTGTT | 7468 |
rs576135481 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873001 | TTCCTTGTGTACTTG[A/G]TGTGTGCTCTCATTC | 7468 |
rs576141766 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979477 | TTCCTCAGAAACGCT[G/T]CTTTTCCATCCTAGT | 7468 |
rs576176696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939223 | AAAAAAAGACATGAG[C/G]AATTGGACATTTGAA | 7468 |
rs576201632 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901454 | CTCAGTTCTCAGCTG[A/G]CTGCTGAGCCAGTTG | 7468 |
rs576256530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928331 | CCTTATAAGGTAAAT[A/T]TAAATTATCTCTGCT | 7468 |
rs576270763 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933701 | GCCCGGCCCTGCAAG[A/G]TGTTTTATGAAGAGT | 7468 |
rs576275002 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978215 | GTTGGCCATGGGTGC[A/G]AGAGGGTGGTCCCTA | 7468 |
rs576314247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883771 | GCTGCATTCCCAGAG[C/T]GAGCAGCATGTGTGG | 7468 |
rs576320938 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931402 | GGAGAGCTGACATTG[-/T]TAAGATTTGAAGATG | 7468 |
rs576338661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922354 | AAACCAAAATGTCAG[A/G]TACTGCGGAATCAAT | 7468 |
rs576354074 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980975 | AAGGCCCCAGGGCCC[C/T]GCTGTCACTTGCCCA | 7468 |
rs576361914 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934536 | GGTTATATTTAAATT[G/T]AATGCTTTAATACAT | 7468 |
rs576373946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890552 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 7468 |
rs576379968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975855 | GCCTGCCCTGCTACC[A/G]TGTGACCCCATCTTA | 7468 |
rs576416003 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980596 | TTGTGACCTGTAAGC[A/G]TGGGGTTCAGGGGTG | 7468 |
rs576441963 | in-del | -/ATG | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929686 | GTGTCATGAAATATT[-/ATG]ATGTTTTTCAGACAT | 7468 |
rs576482395 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935684 | GCCAAGATGGTAATA[-/C]CCCCGTCTCTACTAA | 7468 |
rs576517415 | snp | C/G | 2.15678e-05 | 0.00328381 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955375 | CTGCGGCACACGCCT[C/G]TCACACTCCCAGGAG | 7468 |
rs576541366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908012 | GCACCAGCCGCATTT[A/C]GGGAAACATCACATC | 7468 |
rs576581444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948691 | AACATTTATATATTT[C/T]CATTCAAAATATGTA | 7468 |
rs576622541 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883693 | CCTTGTTTGTTGTCC[C/G]CATCTGCTCTCCCAG | 7468 |
rs576631190 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914844 | TGGCCTTTCACCCAA[A/C]CCCCAGCAGCTTGAA | 7468 |
rs576634486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1883215 | ATTTACATTACCTTC[C/T]ATTTCAGGTTCAGAA | 7468 |
rs576642327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975784 | CAACCATTCTCCCTG[C/T]GAACATGACTGTTGA | 7468 |
rs576668742 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973852 | TGATTTCTCCCCACG[C/T]GGTTGTGCGGTGGAT | 7468 |
rs576679347 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980550 | TAAAAACTGCAGTGT[C/T]TTTGGACCTGAGAGT | 7468 |
rs576679446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975061 | GGGCAGAGTGGCCAT[C/T]GCTGAGGGCTGCGTG | 7468 |
rs576679863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914147 | CGTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 7468 |
rs576697972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953741 | CCTAAAGATGCTTAA[C/T]TATAGGAGAGGGGCA | 7468 |
rs576705403 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961070 | CGTTGGGGAGCTGAT[C/T]GACGAGGAGGAGTGC | 7468 |
rs576722518 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869813 | TGAGCCACTGGCCTT[A/G]GCTCCATTTTGAATT | 7468 |
rs576788615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1962617 | GGTATACTGATGTTC[C/G]TTATAGTATTCTTCC | 7468 |
rs576796984 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916117 | GCTGCTCTCTGAGGC[A/C]ACTGATGCTCCTGTC | 7468 |
rs576816785 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979665 | CTTCTCACCTGGGCC[G/T]ATCTTCTGAACTCGC | 7468 |
rs576841528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947016 | CAAGAAATGACTGAG[A/G]TAGGGGTGGGGGTCC | 7468 |
rs576866536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915584 | TTTGGATTCATTCAT[A/C]CTGGATGCTTCCCTG | 7468 |
rs576867005 | snp | A/G | 1.65616e-05 | 0.00287759 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955896 | CTTTTCTGTTCACAT[A/G]TGTTCGCTTTACAGT | 7468 |
rs576874274 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979329 | CTTTCTGGCTCTCAG[C/T]GCCGTCGCCACTCGG | 7468 |
rs576906589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961666 | GATAGGAAGATTTGT[A/G]TAAAAGTGGGCATGG | 7468 |
rs576930273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921332 | GGCATGGTGGCGTGC[A/G]CCTGTACTTCCGGCT | 7468 |
rs576934512 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962926 | CATGCTCTGTCAGGG[C/T]GCACCACCCAGGGGA | 7468 |
rs576966744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969622 | TGAGGTGGGAGTATC[A/G]CTTGAGCCCAGGAGG | 7468 |
rs576971807 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890384 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 7468 |
rs576975475 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1968735 | TACATAGTAACAACA[A/C]GGAAAGGCTCCCACA | 7468 |
rs577029296 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876125 | AGGCTGAGGCAGGAG[A/G]ATGGTGTGAACCTGG | 7468 |
rs577036958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1889695 | TAGTAGAGAGAGTTT[C/G]ATCATGTTGGTCAGG | 7468 |
rs577041638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933172 | GGGCCCCCACGCTTT[A/G]GCTGCTGACTCTTCT | 7468 |
rs577076505 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946198 | AAGGTTTCTTAAAAT[A/G]CTCACAAAGCTGTTA | 7468 |
rs577081279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1927609 | CTATAATCCCAGCTA[C/T]TCAGGAGGCTAAGGT | 7468 |
rs577122883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939165 | TGTTTTGCATGAGGT[A/G]CTTGACTGGCTTTTA | 7468 |
rs577124572 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925959 | AGCCATGTGCCACCA[A/C/T]GCCTGGCTAACTTTT | 7468 |
rs577148673 | snp | A/C/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869544 | TTTAGTAGAGACGGG[A/C/G]TTTCACCATGTTAGC | 7468 |
rs577156578 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WHSC1 | GRCh38.p7 | 4:1895630 | ACTGTCCCATGCCTG[A/G]CTCCTGGAGGATCTC | 7468 |
rs577194795 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | WHSC1 | GRCh38.p7 | 4:1902563 | CAGCAGTATTGAACC[-/T]CATGCTTTTGCTTGG | 7468 |
rs577212242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894936 | TCCCATAATTCCCCA[C/T]CCTCCTTTTTCTTCC | 7468 |
rs577251424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938636 | GGGGCTGGTGAAGGG[A/G]AACAGGGCAGGGGAG | 7468 |
rs577263318 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977503 | AAAAGAGGCCAGGTG[C/T]GGGGGCTCATGCCTG | 7468 |
rs577301572 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943736 | ATTCTCAAAAAAAAA[A/C]CCCACGAAATTTAAA | 7468 |
rs577314816 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946394 | TGCCTCAGCCTCCCG[A/C]GTAGCTGGGACTACA | 7468 |
rs577348050 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946172 | AGAAACTGAGGTAAC[-/TG]TCATTAGAAAAGGTT | 7468 |
rs577348119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WHSC1 | GRCh38.p7 | 4:1894149 | TTTTGTAGAGACGGC[A/G]TCTTACTATGTTGGC | 7468 |
rs577369569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900252 | CCAGCTGCCTCACAC[A/G]TATTAGCTCTTTTAA | 7468 |
rs577371936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1907057 | TTACTCTCTGCGGTT[A/G]AGGCTGGGACTCAGG | 7468 |
rs577386741 | in-del | -/AAG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971479 | TTCAGCACTGTCGAA[-/AAG]AAGGACAGAATACAC | 7468 |
rs577387143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1875350 | GGAGTCATATGATCA[C/T]GGCTCATTGCAGCCT | 7468 |
rs577401758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914104 | CTCAGCTTGCTGCAA[C/T]CTCTGCCACTTGGGT | 7468 |
rs577405766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934123 | AGAGTTTCGTTCTTG[A/T]TGCCCAGGCTGGAGT | 7468 |
rs577430804 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973898 | GTGGAGGCCGGGGCC[A/G]TCCATTCCCTGCTGC | 7468 |
rs577436348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906545 | GTGCCGCAGCCCAAC[A/T]TATATATCATTGCAT | 7468 |
rs577454122 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939254 | CGCTAGCTGATGATA[C/T]AAGAGCATTGTTACT | 7468 |
rs577456886 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901989 | TGGCCCTGACACTCG[A/G]ATGAGTATAAGCCAT | 7468 |
rs577457984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920388 | CGGGAGGCCACAGTG[A/T]GCTGAAATCATGCCG | 7468 |
rs577471143 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908512 | CAGTTCAGAAGGAGT[C/T]AAGCCTGGGTAGATA | 7468 |
rs577475586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1919903 | ATTACACCACTGCAC[G/T]CCAGCCTGGCGACAG | 7468 |
rs577490886 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904904 | GGGAGGCCGAGGTGG[A/G]TGGATCACTTGAGGT | 7468 |
rs577499498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874563 | CCATTTTAATGCCGA[C/T]ATCTGGCCTGTTTGC | 7468 |
rs577535587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1936073 | TGGGAATACTAAACA[G/T]GCTGTGCAGGAAAAG | 7468 |
rs577545379 | snp | A/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941461 | GGTCGAGGCCTGCCC[A/T]TGAGTCAGGGGAGCT | 7468 |
rs577551909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892575 | CCACTGATAACTCTT[C/T]TTTTTTTTGAGACGG | 7468 |
rs577635318 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982408 | CATAACTGACTGACT[C/T]TGGAAAAATGCTTTC | 7468 |
rs577646990 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923059 | AGGTCTGCACTGGAC[A/G]TGGTGCTGGGACCAC | 7468 |
rs577649783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935566 | AAAATTGTCACTAAA[A/G]ATAACCTCTTTGGCC | 7468 |
rs577680848 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897681 | ACTCAGGCTGGAGTG[C/T]AGTGGCGTGGTCTTT | 7468 |
rs577710904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1929014 | GGGAACACTGGTGGA[A/G]TGCTGGGGGTCAGAG | 7468 |
rs577721443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928499 | CCATACAGTTTCACC[A/G]TGAAGCTCGGAGACG | 7468 |
rs577757212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1898457 | ATCACGAAGTCAGGA[A/G]ATCGAGACCATCCTG | 7468 |
rs577771710 | snp | A/G | 0.000247107 | 0.0111127 | missense | WHSC1 | GRCh38.p7 | 4:1904280 | ACCTGTTGAAATACA[A/G]CGTTGGTGATTTGGT | 7468 |
rs577783029 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886998 | ACATTCCCAATATTG[C/T]GGTGGTTTGATGATC | 7468 |
rs577785181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957545 | CGCCTGCCTCGGCCT[C/T]CCAAAGTGCTTCGAT | 7468 |
rs577797041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1897330 | TACAAAAAAAGGGTT[A/G]AAAAGTTAGCTGAGC | 7468 |
rs577833141 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903976 | CCTGAACTCGTGATC[C/T]GCCCACGTTGGCCTC | 7468 |
rs577854026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917529 | CATCCTCTGCCCCTC[C/T]GGGTTCAAGCGATTC | 7468 |
rs577869173 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | WHSC1 | GRCh38.p7 | 4:1964636 | AGGTGCGCTGCGCTG[-/C]CGTTGTTATCACACC | 7468 |
rs577887332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917121 | TTTGTTTTGAACTTA[C/T]ACTTGCTCGAAATAT | 7468 |
rs577901538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957036 | TGGACTTATGTGTTT[C/G]CTGCGACTGTCGGCA | 7468 |
rs577920073 | in-del | -/TTATT | 0.00239808 | 0.034544 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879207 | CAACACTTTTTAAAA[-/TTATT]TTATTTTATTTTATT | 7468 |
rs577933474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872175 | AAGCCGGGCCGCGGT[C/T]CGGCCCTTGGCAGGT | 7468 |
rs577967449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1963586 | TAGTAAAAAAGAAAT[A/G]CCAGGTTGAGCATTT | 7468 |
rs578024493 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870686 | TCCCGCAGCCGCGCC[C/T]AGCTCCGGGTCGGAC | 7468 |
rs578069246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WHSC1 | GRCh38.p7 | 4:1878638 | GAATACATACACAGC[C/G]CTCAGTACTTCGTAT | 7468 |
rs578087260 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924250 | GGCATGTTGGGGGAG[C/G]GTGCAGTGGCAAGCT | 7468 |
rs578102666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934046 | TTCAACTTAAATTCC[A/G]CAAGTCTTTGAATGT | 7468 |
rs578103871 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981613 | CTTCAGGCACCTGAA[A/G]TGAGAACCCAGCTGT | 7468 |
rs578109498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976856 | GTTCCACCAGCCGCA[C/T]ATTCTAGATCTCTGC | 7468 |
rs578113379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891124 | ATGTCGAGTTCTTGG[A/G]CTCAAGCAATCCTTC | 7468 |
rs578145510 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981076 | ACTTTGGGGAGCAGA[C/T]ATTAACTTATTTTTG | 7468 |
rs578184303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940798 | TGTGCCTCAGTTGTT[A/T]CCACTCATTAGAGGA | 7468 |
rs578191582 | in-del | -/GTGGTGGCTGTCTTGTGAGGC | 0.0111196 | 0.0737302 | intron-variant | WHSC1 | GRCh38.p7 | 4:1928588 | CCGCAGAAGCCGTCT[-/GTGGTGGCTGTCTTGTGAGGC]GTGGTGGCTGTCTTG | 7468 |
rs578207495 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960032 | GCCCTAATAATTTTA[-/T]TTTTTTTTTGGAGAT | 7468 |
rs578211655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976300 | TTTTTCACGCTGAGT[C/T]GAGTGAGTCTAAGGA | 7468 |
rs578261917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949046 | CTCTGAGTGGGGCCC[C/T]AGACAGTGTGGCCAC | 7468 |
rs745314059 | snp | C/T | 4.94841e-05 | 0.00497389 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951232 | AGCATCCGCTATGTC[C/T]GTGCTGGTGTCTGAC | 7468 |
rs745316255 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973716 | GTTGTGTCAGAGGCC[A/G]CGTGTGAATAGTGAC | 7468 |
rs745317806 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900762 | CAACGGGAAGACTCC[A/G]AGCTGCGAGGTGAAC | 7468 |
rs745329555 | snp | C/T | 1.6617e-05 | 0.00288239 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955935 | TATTGAAATTATTAT[C/T]GCTGTCTCTGAGGAG | 7468 |
rs745348599 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939712 | AAATCGGGCTTCCAC[A/G]GCAGCATCTTCAGCT | 7468 |
rs745354007 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922868 | TAGGCGGAGGTTGCA[A/G]TGAGCTGGGATTGTG | 7468 |
rs745430759 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923876 | AAATTGCTGAAGGGT[A/G]TGCAGATTCTATCAC | 7468 |
rs745454690 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891495 | TATCAGAGTGGGCTT[C/T]AGCTGACATCTAAGC | 7468 |
rs745459070 | in-del | -/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941882 | CCAATGCTGAATGCC[-/T]TGTTAGCATATGAGG | 7468 |
rs745462645 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903590 | GTGAGAATTCCTTTT[C/T]GACCAGTTGAATAAA | 7468 |
rs745473741 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937857 | CTTGAGAAAAGCTTC[A/G]TGATCCCTTCTCCCA | 7468 |
rs745505464 | snp | A/C | 1.68658e-05 | 0.0029039 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935133 | ACATTTTCCCCATTC[A/C]CCATTCCAAGGTAAT | 7468 |
rs745552415 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877708 | CACACGGGCCTCTTG[A/C]CTGCTCTGAAGCCCT | 7468 |
rs745560249 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973045 | TTTTATTAGAGACAG[C/T]TTCACCATGTTGGCC | 7468 |
rs745574055 | snp | C/T | 1.67326e-05 | 0.00289241 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952096 | GCTTACCCGCCTGCT[C/T]TGCCCCCGCAGCTGT | 7468 |
rs745579990 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981803 | GTTAATGCAAATGAC[C/T]GTCAGTTGCCAAATA | 7468 |
rs745592357 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902658 | TGCACAGGCTGTTCA[C/G]GAACTCCTGACCTCA | 7468 |
rs745593402 | snp | G/T | 1.64765e-05 | 0.00287019 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935193 | GAGGATACAGGACCC[G/T]ACAGAAGATGCTGAA | 7468 |
rs745607796 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978479 | GCCAGGGAGCCCGCC[C/T]GGGCTGTGGTAGACA | 7468 |
rs745624747 | snp | C/T | 0.000231869 | 0.0107648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959755 | GGTATGTGTCGTTAT[C/T]CCCTCCCCTGCTTTT | 7468 |
rs745645297 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931218 | CGGCTGTAGTCTGCA[C/T]CTTACAGGGGTCCGG | 7468 |
rs745664737 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | WHSC1 | GRCh38.p7 | 4:1959628 | CGCAGGTGTGTCCCG[C/T]GGGCGAGTTCTGCCA | 7468 |
rs745670398 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948757 | TGTAGGAAATCTCTC[C/T]AAGTGGAAACGTGCT | 7468 |
rs745688299 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932177 | CACGGTGGCTCACAC[C/G]TGTAATCCCAGCACT | 7468 |
rs745729169 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910285 | GGCTGGAGTGCAGTG[A/T]CACAATCTCGGCTCA | 7468 |
rs745769801 | in-del | -/TGATGAA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894304 | TTCAATACAATGTAT[-/TGATGAA]CTAGATGATTTGTTT | 7468 |
rs745794953 | in-del | -/GT | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979809 | TCACCACCGACTGAA[-/GT]GTGTGTTTACTGATG | 7468 |
rs745830694 | snp | A/G | 1.6863e-05 | 0.00290365 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916828 | GACTAGTTTCATCCC[A/G]GATTCTAACTTTCAT | 7468 |
rs745846601 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962288 | TCCTGGGTTAAAAGA[C/G]ACTAAAGAAGTACCC | 7468 |
rs745850455 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963869 | GAAAAAAAATTAGCC[A/G]TGCCTGTGATTCCAG | 7468 |
rs745857741 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972854 | GAAAGTTTTTGACAC[-/AT]TTTTTTTTCTTTTTG | 7468 |
rs745865096 | snp | A/G | 3.41705e-05 | 0.00413329 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955132 | GAGTCAGTGTTTGGG[A/G]TCCTTAGGGTGTGTT | 7468 |
rs745914267 | snp | C/T | 9.51656e-05 | 0.00689737 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978903 | GAGAGTCACAGAGGG[C/T]AAATAGCGCCAGGCG | 7468 |
rs745921448 | snp | A/G | 3.3243e-05 | 0.00407681 | missense | WHSC1 | GRCh38.p7 | 4:1918462 | CTGGAGAGTCACCCC[A/G]ACATAGGGAAGAGTA | 7468 |
rs745927376 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944774 | AATTGCCCCACCTGC[C/T]CTAGATGGATCTTTG | 7468 |
rs745928619 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974828 | ATAACATGCGATTGC[C/T]AACACTTGACCGAAT | 7468 |
rs745955509 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927611 | ATAATCCCAGCTACT[C/G]AGGAGGCTAAGGTGG | 7468 |
rs745957331 | snp | C/T | 1.6522e-05 | 0.00287414 | missense | WHSC1 | GRCh38.p7 | 4:1955280 | GCCCACTTCACTGCT[C/T]GGAAGGGGAAGCGAC | 7468 |
rs745966514 | snp | C/G | 1.88258e-05 | 0.00306799 | missense | WHSC1 | GRCh38.p7 | 4:1978844 | AAGCCCCCCCCAGAG[C/G]CAGGGAAGCCGAAGG | 7468 |
rs745968741 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956548 | GGCTCTTGGGGGCTC[A/G]CTTTACCTTTCAGTG | 7468 |
rs745972392 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant, utr-variant-3-prime, synonymous-codon | WHSC1 | GRCh38.p7 | 4:1942342 | CACTGGTAACAGCTT[C/T]TGTGGGAGCCCACAC | 7468 |
rs745978472 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976903 | ATGTGGTGACGGGGT[A/G]GCCCCTGGAACCTCC | 7468 |
rs745978663 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915216 | CGCCTCCTGGGTTCA[C/T]ACCATTCTCCTGCCT | 7468 |
rs746030613 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898424 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC | 7468 |
rs746073848 | snp | C/G | 1.6486e-05 | 0.00287102 | missense | WHSC1 | GRCh38.p7 | 4:1900986 | AAGGGATTGGGACAC[C/G]CCCTAACACTACCCC | 7468 |
rs746075714 | snp | A/G | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982343 | CTGACCCGCTGGGGA[A/G]AGGCAGTGCCACCTT | 7468 |
rs746098129 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907186 | ACCATCACCTTCATG[A/G]AAAGGTCTTAATGCA | 7468 |
rs746125492 | snp | A/T | | | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1957967 | TCGTTTTCGTGAAAT[A/T]AAGCTTCAGAGGGAA | 7468 |
rs746127427 | snp | A/G | 1.6916e-05 | 0.00290822 | missense | WHSC1 | GRCh38.p7 | 4:1918564 | GTCTCCATGCCACGA[A/G]GCAGGAAGGGAGATG | 7468 |
rs746138677 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952808 | GGACACCTGCACAGC[C/T]GTGGCCCTTCCTGCC | 7468 |
rs746146123 | snp | C/T | 6.72857e-05 | 0.00579986 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956169 | GGGGGTCAGAGGGAT[C/T]GGAAGAGTCTTCAAA | 7468 |
rs746205513 | snp | C/G | 0.000139978 | 0.00836476 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953202 | GGTTGGAAACAGGGC[C/G]AGGTGCTTTAGCAGC | 7468 |
rs746213666 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886649 | ATCCTAGCCAACGTG[A/G]TGGAACCCCGTCTCT | 7468 |
rs746213971 | snp | C/T | 1.96331e-05 | 0.00313307 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976724 | GCTGTGTCTGTGTGG[C/T]AGGCTCCTGATGGCG | 7468 |
rs746245778 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980962 | CACCTTAGAGTCGAA[G/T]GCCCCAGGGCCCCGC | 7468 |
rs746260679 | snp | A/G | 1.64833e-05 | 0.00287078 | missense | WHSC1 | GRCh38.p7 | 4:1957950 | CTGCAAGAAGCTGAA[A/G]CTCGTTTTCGTGAAA | 7468 |
rs746279426 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938417 | TTTTTTTTTTCTTTC[-/TT]TTTTTTTTTTTTTTT | 7468 |
rs746288420 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901810 | TCCCTGAGGCCTAGG[G/T]ATGTGTCTTTTGCCT | 7468 |
rs746342656 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929447 | GCCTTCACTTGCCGA[A/G]GTCCACAGAACTACC | 7468 |
rs746359628 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883941 | AGGCTGAACTGTCAC[A/G]AGAGCATGGAGAAGC | 7468 |
rs746362705 | snp | C/T | 1.65258e-05 | 0.00287448 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938515 | TGGAGGCAGCCTCCT[C/T]GCTCAAGAGCCAGGC | 7468 |
rs746372645 | snp | A/G | 1.65154e-05 | 0.00287358 | missense | WHSC1 | GRCh38.p7 | 4:1916997 | AAAAATTATGCCAGG[A/G]AAGTGCCAAGCAGGC | 7468 |
rs746400962 | snp | C/T | 3.53245e-05 | 0.0042025 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953269 | GGCTCAGAACTGCAA[C/T]TTAATTCTTGTTCTT | 7468 |
rs746403018 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972623 | ACTGATGCCTCCCCT[C/T]ACACCACTTATAAAG | 7468 |
rs746421387 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884647 | TCTGCCTGCCTTGGC[C/G]TCCCAAAGTGCTAGG | 7468 |
rs746421544 | snp | A/G | 1.71578e-05 | 0.00292893 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978639 | GTGTTCTGTTGCAGG[A/G]AAGTGGGAATGTCCT | 7468 |
rs746424531 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965146 | AACTATCCCTAAAAG[A/G]AAGGCCAGATGATAG | 7468 |
rs746426053 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938426 | TCTTTCTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs746430866 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950447 | GGAGAACAAGTGAAC[-/TG]TGAAATATCAGGACA | 7468 |
rs746459297 | snp | A/G | 1.67058e-05 | 0.00289009 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935141 | CCCATTCCCCATTCC[A/G]AGGTAATGTAAATGG | 7468 |
rs746488285 | snp | A/T | 3.6667e-05 | 0.00428161 | missense | WHSC1 | GRCh38.p7 | 4:1976512 | AGGAAAAGGGCAAAA[A/T]GACCAAGAAGAAAAC | 7468 |
rs746504975 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963859 | CTACAAAAAAGAAAA[A/T]AAATTAGCCGTGCCT | 7468 |
rs746513080 | snp | A/G | 1.66785e-05 | 0.00288773 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952104 | GCCTGCTCTGCCCCC[A/G]CAGCTGTGTGAGAAG | 7468 |
rs746514547 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962544 | TTTGTGTGTGTATAC[A/G]TATATCCATAAATAG | 7468 |
rs746529986 | snp | C/G | 0.000387163 | 0.013908 | missense | WHSC1 | GRCh38.p7 | 4:1956137 | TACATGGAGGGGGAC[C/G]GGGGCAGCCGCTACC | 7468 |
rs746533711 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969045 | GAAAGTACTGGAGAC[C/G]TGCAGTGTCACCCGG | 7468 |
rs746555710 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941214 | TACAGTTCCAAAGAA[A/G]AATATTAAACATTTT | 7468 |
rs746561982 | in-del | -/TC | 0.000142676 | 0.00844498 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918121 | GTGAAACTTACAGTG[-/TC]TCTCTTTTTTTTTTC | 7468 |
rs746586392 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911498 | AAGGCTGAGGCATGA[C/G]AATCGCTTGAGCCCA | 7468 |
rs746594142 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898031 | TTTTTCCCTCCTCCT[C/T]CTGGGTGGAACTCCA | 7468 |
rs746642766 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893247 | CCGAGACGGGTAGAT[C/G]ACCTGAGGTCAGGAG | 7468 |
rs746664003 | snp | A/G | 1.66635e-05 | 0.00288643 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916857 | ATTCTCTAACATTTT[A/G]TTTTAAAAACTAGGT | 7468 |
rs746717100 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936377 | ATTTCTATTTTATTC[A/G]ATAATAGTTCTGGCC | 7468 |
rs746720577 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | WHSC1 | GRCh38.p7 | 4:1935203 | GACCCTACAGAAGAT[A/G]CTGAAGCTGAGGACA | 7468 |
rs746743921 | snp | A/G | 1.64868e-05 | 0.00287109 | missense | WHSC1 | GRCh38.p7 | 4:1916970 | TAGCTTTTGAAGGAG[A/G]AGGACAGTTTGAAAA | 7468 |
rs746753670 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979915 | GACAACTTAGGGAGC[C/T]CCGTAGGGCGCTGCA | 7468 |
rs746759119 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886245 | AGGATCTCACTGTGT[-/G]GCCAGGGCTGGAGTG | 7468 |
rs746763078 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971239 | AAGGTGAAGTCGAAG[-/A]AAAGGAGTTGTTCTC | 7468 |
rs746765467 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933892 | TCTTGGATTAACTGC[C/T]ATTCCTGGGAACACC | 7468 |
rs746770939 | snp | G/T | 2.06439e-05 | 0.00321271 | missense | WHSC1 | GRCh38.p7 | 4:1978858 | GCCAGGGAAGCCGAA[G/T]GGGAAGAGGCGGCGG | 7468 |
rs746862738 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898949 | TTCCGTCCATTTTCT[C/G]TCTGCTTTTGGTTGC | 7468 |
rs746869747 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889248 | GCCACTCAGGCTGGA[G/T]TGCAGTGGTGTAATT | 7468 |
rs746882486 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919912 | CTGCACTCCAGCCTG[A/G]CGACAGAATGAGACG | 7468 |
rs746891959 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949927 | AGAGTCCCTGGTGGG[A/G]TTGGCTTTTATTTTT | 7468 |
rs746926553 | snp | C/T | 6.59413e-05 | 0.00574163 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951092 | GGACAGCCCGGGAGA[C/T]GAGCCCTCGGAGTCC | 7468 |
rs746948797 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887598 | CTCCTACTTCAGGCT[A/G]CCAAAGTGCTGGGAT | 7468 |
rs746979750 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956897 | TAGCTCCATGCTGCC[A/G]GAAGCTTTGCAGGCT | 7468 |
rs746980079 | snp | A/G | 1.67548e-05 | 0.00289432 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951036 | CCCGCTGTGTTCTGC[A/G]ACTAGTGAACTGTCA | 7468 |
rs747003542 | snp | A/G | 2.10431e-05 | 0.00324363 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955371 | GTGTCTGCGGCACAC[A/G]CCTCTCACACTCCCA | 7468 |
rs747012945 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979336 | GCTCTCAGCGCCGTC[A/G]CCACTCGGGAGAGGC | 7468 |
rs747026813 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977619 | CGTCTCTACTAAAAA[C/T]ACAAAAATTAGACTG | 7468 |
rs747032517 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929666 | TTGAATTTCCTGTAA[C/T]TTTTGTGTCATGAAA | 7468 |
rs747054111 | in-del | -/TTC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915049 | TTCATCTTAATTTTT[-/TTC]TTCTTTCTGGGAGAT | 7468 |
rs747064254 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947174 | AGGCTCCTCCCCAGC[A/C]CACTCCCTGTGGGAT | 7468 |
rs747066013 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1957976 | TGAAATTAAGCTTCA[A/G]AGGGAAGCCCGAGAA | 7468 |
rs747112223 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915530 | TCTTCCCTTGCCTTA[C/T]GTCTGTGGCCCTGCA | 7468 |
rs747116757 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966794 | TACTAGTTTTACTCA[A/T]GAATTACTGGCTTGT | 7468 |
rs747137848 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885195 | GCTTGTTTGTCCACT[A/G]TCTACCTTTTTAGGC | 7468 |
rs747140498 | snp | A/C/G | 8.23928e-05 | 0.00641801 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974979 | CACTCGTGTGGGCCT[A/C/G]TTTGCCGTCTGTGAC | 7468 |
rs747140730 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892395 | AAGGTCCATGTGGTC[C/G]TATAGGGGCTGTTCA | 7468 |
rs747142703 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908907 | CCTGCCTTGGCCTCC[A/C]AAATTGTTGGGATTA | 7468 |
rs747174886 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931097 | AGGGGAGGGAAGGTC[A/G]TCTCTTGGATTCCAG | 7468 |
rs747187711 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945873 | GTCGTTATGACTTTG[A/G]CAACTTGCTTCATTT | 7468 |
rs747220169 | snp | A/G | 1.83815e-05 | 0.00303157 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901268 | TATTTAGGAGACGTT[A/G]TGTAAGGGGTCATGT | 7468 |
rs747222716 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896399 | GGCAGTGTAGCTAGA[C/T]AAGGTCTTGCTGAGT | 7468 |
rs747276503 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979613 | TCAACGTGTAGTTTA[C/T]GCGGAGCACTTTCGA | 7468 |
rs747297385 | snp | A/G | 5.38779e-05 | 0.00518999 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953216 | CCAGGTGCTTTAGCA[A/G]CATGGCTGCCTCTGA | 7468 |
rs747319484 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981929 | GGTGTGAAATGCCCC[A/G]TCAGAAATTAAATAC | 7468 |
rs747328730 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1954776 | TCTGTACTTCTTGAC[A/G]CCAGTGGTTCTTTAT | 7468 |
rs747344990 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939915 | GATGTTTTAGGGCCT[A/C]TTGGCTAACTCAGAT | 7468 |
rs747345820 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881354 | TGCAACCTCCGCCTC[C/G]TGGGTTTACGCCATT | 7468 |
rs747353321 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973830 | TGTTACGCTTTATGT[A/G]GCCTTTTGATTTCTC | 7468 |
rs747356821 | snp | G/T | 3.30994e-05 | 0.004068 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938545 | CAGGTAATGTGGTCA[G/T]CGCCCTTTCCTTCTT | 7468 |
rs747360048 | snp | A/C | 3.30469e-05 | 0.00406477 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978759 | AGCCTTCAGCTGCAC[A/C]CCGGACGGGCGGTCC | 7468 |
rs747408787 | snp | A/G | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952371 | CCCTCTCTGGAGCTT[A/G]TAGCCCACAGCTGGC | 7468 |
rs747413223 | snp | C/T | 1.6661e-05 | 0.00288621 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978669 | TTGGCATCATTGTGA[C/T]GTGTGTGGCAAACCT | 7468 |
rs747417423 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904547 | TGCCATTTCTTTTTA[A/T]ATTCAACTCAAATAT | 7468 |
rs747460333 | in-del | -/C | 1.71625e-05 | 0.00292933 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959462 | GACAGCTTACTCCTT[-/C]CCCTGCAGGTGAATA | 7468 |
rs747469766 | snp | A/T | 1.65274e-05 | 0.00287462 | missense | WHSC1 | GRCh38.p7 | 4:1918298 | CTCAAGTAGCCAAGG[A/T]GGCTGGCATTGCTGC | 7468 |
rs747479237 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910901 | TGTCCTTTGTTTCCC[A/G]GGGAGCTCTGTGGTC | 7468 |
rs747480895 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916621 | TGGTGGGATTACAGG[C/T]GTGAGGGACTGCGCC | 7468 |
rs747485914 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869952 | ATTTCCTAGAGTCAA[A/G]CTCAGCTGACTCCAT | 7468 |
rs747535030 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957928 | CTATTTCATTGACTT[C/T]TTAGCACTGCAAGAA | 7468 |
rs747548214 | in-del | -/A | 0.000279004 | 0.0118078 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938441 | TTTTTTTTTTTTTTT[-/A]AAATAATAGAGAGAC | 7468 |
rs747566508 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968473 | CTTTGTTAAAGTATA[C/T]ATGTGACGTCTACAT | 7468 |
rs747572764 | snp | A/C/T | 9.38528e-05 | 0.00684976 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974634 | CTGTCCTGTCCTCCC[A/C/T]GGCGCTCACTAAGGC | 7468 |
rs747597002 | snp | G/T | 2.03722e-05 | 0.0031915 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938409 | TTCTTTTCTTTTTTT[G/T]TTCTTTCTTTTTTTT | 7468 |
rs747603711 | snp | A/G | 1.67643e-05 | 0.00289515 | missense | WHSC1 | GRCh38.p7 | 4:1918171 | TCAGGGAAATTGAGG[A/G]CCCAGTGGGAAATGG | 7468 |
rs747629318 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951614 | GCTGTGGGCTGAGGG[A/G]GCCATCACTAGACCT | 7468 |
rs747631291 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932214 | GGCCAAGGTGGGTGG[A/T]TCACTTGAGGCCAGG | 7468 |
rs747643470 | snp | A/C/T | 9.05674e-05 | 0.00672871 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976697 | GGGTGTGCAGCCTCG[A/C/T]GGTGGCTTGCAGCTG | 7468 |
rs747643755 | snp | A/C | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980083 | CCAGGGCACCTACTG[A/C]GAGGTGCGGTCCTGG | 7468 |
rs747648542 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893311 | GTCTCTACTAAAAGT[-/A]ACAAAAAAATGAGCC | 7468 |
rs747677715 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972179 | CCCTGCCCTCCTCAT[A/G]TATGCAGAGCCACAA | 7468 |
rs747692965 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1950198 | TGTTGATGTTGCTTG[A/T]CAGGTGAGGGTGAAA | 7468 |
rs747693753 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900138 | CTGCCTGATACCTCA[A/G]CTGTAACAGGAGGGA | 7468 |
rs747724723 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918125 | AAACTTACAGTGTCT[C/T]TTTTTTTTTTCCCAG | 7468 |
rs747732345 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911687 | ACAACTGGTTAATTA[C/T]TGGTAAAATAAAAAC | 7468 |
rs747741669 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913357 | CGTGGGGGAGTTAGA[A/G]AAGACTCTGCTCCAC | 7468 |
rs747743020 | in-del | -/T/TT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938416 | TTTTTTTTTTCTTTC[-/T/TT]TTTTTTTTTTTTTTT | 7468 |
rs747771794 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967577 | GCGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA | 7468 |
rs747792814 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882498 | GAAACCCCGTCTCTA[C/T]TAAAAACACACAAAA | 7468 |
rs747816605 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899159 | CACATGAAGCTGAAC[C/T]GGGACTTCAACATTT | 7468 |
rs747832916 | in-del | -/TT | 5.46784e-05 | 0.00522841 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918126 | AACTTACAGTGTCTC[-/TT]TTTTTTTTCCCAGCT | 7468 |
rs747834783 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967469 | CATAATCCCAGCTAC[C/T]CAGTAGGCTGAGGCA | 7468 |
rs747858571 | snp | A/G | 1.64988e-05 | 0.00287213 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916986 | AGGACAGTTTGAAAA[A/G]TTATGCCAGGAAAGT | 7468 |
rs747861024 | snp | C/T | 1.66161e-05 | 0.00288232 | missense | WHSC1 | GRCh38.p7 | 4:1955302 | GGAAGCGACACCACG[C/T]CCACGTCAACGTGAG | 7468 |
rs747865163 | snp | C/T | 1.6755e-05 | 0.00289435 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961163 | CAAGGTAATGCGGAA[C/T]TCCACTGTGAGCTTC | 7468 |
rs747885475 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964029 | TTTGAAAAGGAGCCC[C/T]ACTTAAACGTTTACA | 7468 |
rs747932211 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921627 | TCTCTACTAAAAATA[A/C]AAAATTTTACCAGCT | 7468 |
rs747953798 | snp | C/T | 2.25894e-05 | 0.00336068 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955381 | CACACGCCTCTCACA[C/T]TCCCAGGAGCCACAT | 7468 |
rs747989668 | snp | C/T | 0.000119682 | 0.00773476 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978925 | CGCCAGGCGGCCGCT[C/T]GGCCGGATCCAGGGG | 7468 |
rs748017880 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889389 | TGTGGAGCTGAGGTT[C/T]TTGCTATGTTGCCCA | 7468 |
rs748028872 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877469 | TCATCTCTTTCTGCC[A/G]TGTTTTTCCTCTGGG | 7468 |
rs748038984 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907847 | TGATCTCTTGACCTT[C/G]TGATCCACCCACCTT | 7468 |
rs748061263 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935845 | CAGCCTGGGCGACAC[A/G]GCAAGATTCTGTCTC | 7468 |
rs748070928 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875982 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAT | 7468 |
rs748075151 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971897 | AGAAACCAGGACTAC[A/C]AGTATGCTTAGCTTG | 7468 |
rs748089712 | snp | A/G | 1.68026e-05 | 0.00289845 | missense | WHSC1 | GRCh38.p7 | 4:1901178 | AGAGGAGCATAAAAT[A/G]TGACTCCTTGCTGGA | 7468 |
rs748110450 | snp | C/G | 1.6516e-05 | 0.00287362 | missense | WHSC1 | GRCh38.p7 | 4:1930740 | ACCAAGTTTGCCCTG[C/G]TGGCCCCTGTCCAGG | 7468 |
rs748152601 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916809 | GCAAAATAGCAGTAG[A/G]TTTGACTAGTTTCAT | 7468 |
rs748156397 | in-del | -/AGGG | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979908 | AGGAAGTGACAACTT[-/AGGG]AGCCCCGTAGGGCGC | 7468 |
rs748165902 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980865 | CTAAGAAAATACTGG[A/G]TCGGCTCATAGATTT | 7468 |
rs748169718 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951207 | TATGTGTGCCAGGTG[A/G]GGAGAAGGCAGCATC | 7468 |
rs748174236 | snp | G/T | 3.30901e-05 | 0.00406743 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975243 | CGCCCCTTAGCTTTT[G/T]AAGAGAAAGGCAGGT | 7468 |
rs748174351 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953332 | TTGTTAGGGATTCAC[C/T]CATGTTTCGTGTGTA | 7468 |
rs748178333 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898584 | AGGAGAATTGAACCC[-/G]GGGAGGTGGAGGTTG | 7468 |
rs748205109 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932045 | GTGTATGCAGGTTCT[C/T]GGGTGTCCTTTAATC | 7468 |
rs748226521 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968832 | ATTAGATGCACGTCC[A/G]ACAGTTGGAAAGATC | 7468 |
rs748230463 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873099 | CGATTACTTTGAGTC[A/G]TTTCCTTTTCTTTCC | 7468 |
rs748242317 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903925 | ATTTTTAGTAGAGAC[A/G]GGGTTTCATTGTGTT | 7468 |
rs748254650 | snp | A/G | 1.65266e-05 | 0.00287455 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978768 | CTGCACCCCGGACGG[A/G]CGGTCCTACTGCTGT | 7468 |
rs748256636 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922870 | GGCGGAGGTTGCAGT[A/G]AGCTGGGATTGTGCC | 7468 |
rs748263797 | snp | G/T | 1.76571e-05 | 0.00297123 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959429 | AAGGGTATTCGGAAG[G/T]CTCTCATGTGTGGAC | 7468 |
rs748293066 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918038 | CATCTGCCTTGACAC[C/G]CATAAGTGCTGGAAT | 7468 |
rs748309032 | in-del | -/GTGGACACAG | 1.73856e-05 | 0.0029483 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974726 | GGGTGTCCTGTCTCA[-/GTGGACACAG]GTGGACACAGGACAC | 7468 |
rs748326816 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897785 | GTGTGTGCCACCAAG[A/C]CTGGCTAATTTTTGT | 7468 |
rs748330151 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931173 | AGGAGGCAGCACTTT[C/T]CTTGCTTCTGAGAGC | 7468 |
rs748347782 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885416 | GAACTGTGATCATTG[C/T]CTTCTCTTTTCTTTG | 7468 |
rs748360474 | snp | C/G | 4.94393e-05 | 0.00497164 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939705 | AGAAGCGAAATCGGG[C/G]TTCCACGGCAGCATC | 7468 |
rs748373242 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888633 | TTGCAGTGGCAATCT[C/T]GGCTTACTGCGGCCT | 7468 |
rs748411778 | snp | A/T | 1.6908e-05 | 0.00290753 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953506 | GCTTCCAACCCTTCA[A/T]ACCCAAGGCCGTCAA | 7468 |
rs748448258 | snp | G/T | 4.96167e-05 | 0.00498055 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939828 | GGTATGAAGGCCATT[G/T]AGCTGCCCACGCTGC | 7468 |
rs748464204 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926594 | TCCCCCCTCAGCCTT[-/C]CTAGTAGCTGGGACT | 7468 |
rs748474407 | snp | C/T | 1.65214e-05 | 0.0028741 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918308 | CAAGGAGGCTGGCAT[C/T]GCTGCAGAGTCTTTG | 7468 |
rs748498733 | snp | A/G | 1.75059e-05 | 0.00295849 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974714 | AGGACTGGTTTGGGG[A/G]TGTCCTGTCTCAGTG | 7468 |
rs748504186 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894352 | AACATAGGGTGCTCT[C/T]TTATTCAGAATATCT | 7468 |
rs748544468 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975850 | TTAGCGCCTGCCCTG[C/T]TACCGTGTGACCCCA | 7468 |
rs748567663 | snp | C/G | 1.64947e-05 | 0.00287177 | missense | WHSC1 | GRCh38.p7 | 4:1900877 | GCCCTGCCCTTTATT[C/G]CAGCCGACAAGCTGA | 7468 |
rs748599545 | in-del | -/ACAC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917311 | CGTATATATGTGTAT[-/ACAC]ACACACAGACAGAGG | 7468 |
rs748635117 | in-del | -/GGCGGAGGGGCT | 0.000128187 | 0.00800482 | cds-indel | WHSC1 | GRCh38.p7 | 4:1978872 | AGGGGAAGAGGCGGC[-/GGCGGAGGGGCT]GGCGGAGAGTCACAG | 7468 |
rs748647456 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949325 | TAGTCCATCTTCCTG[A/G]AAAAGGTGAGGAAAC | 7468 |
rs748656196 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874020 | AGGCACACTCAGCCT[G/T]CCTGGCTCTGCCCTG | 7468 |
rs748673417 | snp | A/G | 4.95642e-05 | 0.00497792 | missense | WHSC1 | GRCh38.p7 | 4:1918415 | CCATGAAGAGAAGGC[A/G]GAGGGCCAAACTGTG | 7468 |
rs748680814 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946619 | ATATTTTAGGACTTT[C/T]TGTCAACGAAATTGG | 7468 |
rs748707745 | snp | C/T | 1.64857e-05 | 0.00287099 | stop-gained | WHSC1 | GRCh38.p7 | 4:1900808 | TTCCTCAGCAAAGCC[C/T]AGCTCTCCAGTAGCC | 7468 |
rs748717808 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893385 | TAAGGCAGGAGAATC[A/G]CTTGAACCCAGCGGC | 7468 |
rs748720584 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877273 | ATTTTTCCGACTCCG[A/G]TTTTACTGTCTTCAG | 7468 |
rs748739512 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980903 | TTATGATGCCCTAAC[C/T]TGGAAGGTTGTTCTA | 7468 |
rs748747132 | snp | A/G | 2.70077e-05 | 0.00367466 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955649 | AATCTGGGCTGAGCC[A/G]TAGCAGACAGGCTAA | 7468 |
rs748767363 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953082 | CCAGCCAGGCTGCCT[A/G]GTAAGATTCTCCTGT | 7468 |
rs748801371 | snp | A/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936232 | TGTCTAGCGTATGGT[A/G/T]CCCATGCATGTAGAA | 7468 |
rs748828977 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900342 | TGTGTCCATGGCCAC[A/G]CTGTAGATTATTAGT | 7468 |
rs748840785 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891452 | CCTAGGGTTGAGACC[C/T]CCTTCTGCTCAGTTG | 7468 |
rs748880605 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948550 | TGTCCGGTGGCTGGG[-/A]AGGGGGTGTGGTGGG | 7468 |
rs748885529 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921903 | CCTGTAATCCCAACA[C/T]TTTGGAGGCCGAGGT | 7468 |
rs748895885 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921781 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 7468 |
rs748905850 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915263 | TGAGGCTACAGGCGC[C/T]CACCACCATGCCTGG | 7468 |
rs748912804 | in-del | -/AGAT | 5.14496e-05 | 0.0050717 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956203 | GGTACGGAGATATTC[-/AGAT]AGAGAGTGAGACAGC | 7468 |
rs748919506 | snp | A/G | 1.64906e-05 | 0.00287142 | missense | WHSC1 | GRCh38.p7 | 4:1900757 | AGTGCCAACGGGAAG[A/G]CTCCGAGCTGCGAGG | 7468 |
rs748922675 | snp | C/G/T | 0.000116053 | 0.00761672 | missense, synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955297 | GAAGGGGAAGCGACA[C/G/T]CACGCCCACGTCAAC | 7468 |
rs748953829 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909709 | ACAGTGGTATGATCT[C/T]GGCTCACTGCAACCT | 7468 |
rs748968237 | snp | A/C | 1.66907e-05 | 0.00288879 | missense | WHSC1 | GRCh38.p7 | 4:1930763 | TGTCCAGGCTGAAGA[A/C]GACTCTGGTAAACAT | 7468 |
rs748981703 | snp | A/G | 1.69896e-05 | 0.00291454 | missense | WHSC1 | GRCh38.p7 | 4:1955764 | AACATCGAGATGCCT[A/G]ACGGCAGCTGGTTCT | 7468 |
rs748981823 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951109 | AGCCCTCGGAGTCCC[C/T]ATACGAAAGTGCAGA | 7468 |
rs748993491 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901473 | CTGAGCCAGTTGAGA[A/G]GTCTAGAGAGGTGAG | 7468 |
rs749005496 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980188 | CCCACTCTCCTGTGA[G/T]ATTTCACTTTAGTTT | 7468 |
rs749028422 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873551 | AGAGTCCTAGAATGA[A/G]TCAGGAAGATAATCT | 7468 |
rs749071040 | snp | C/T | 1.69827e-05 | 0.00291394 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975426 | GGCGCCCTCCTTCCC[C/T]CCAGGCTCTGTGTTG | 7468 |
rs749081046 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946142 | TGATAAAGCTAAATT[A/G]TAGTCTTTTGCCAGA | 7468 |
rs749121570 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947391 | GTGCAGGTTAGAAGA[C/T]GACTGTGGTGTGCAG | 7468 |
rs749123768 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875280 | AGTATAGCTTTTTAC[-/T]TTTTTTTTTTTTTTT | 7468 |
rs749162062 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910039 | TTTGAAAACTGAGGT[A/G]TAATATACATGCAAA | 7468 |
rs749169262 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907950 | AGCTTTCGTGGCACT[A/G]TTACCCCCAAATACG | 7468 |
rs749203286 | snp | C/T | 0.000137151 | 0.00827989 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904166 | GGTCTTCTGGATACA[C/T]AGGTAGTGATTGGAT | 7468 |
rs749212102 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877626 | ATGCTGTGCCTGACT[C/T]CTGCCTGTTTTGGGA | 7468 |
rs749230159 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878974 | GTAGTTGCTGGTACT[A/G]TTACCTCTCTGTGAA | 7468 |
rs749245568 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904266 | AAGAGACAAAGACCA[C/T]CTGTTGAAATACAAC | 7468 |
rs749296586 | in-del | -/CTGAC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931294 | AGAAGGGTGACTGGA[-/CTGAC]CTTGAATTCAGGTAT | 7468 |
rs749296789 | snp | C/T | 1.71079e-05 | 0.00292466 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935124 | TTTTCATGTACATTT[C/T]CCCCATTCCCCATTC | 7468 |
rs749348112 | snp | A/G | 3.46548e-05 | 0.00416248 | missense | WHSC1 | GRCh38.p7 | 4:1978826 | AGAAGCACCAAGACT[A/G]AGAAGCCCCCCCCAG | 7468 |
rs749350147 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919686 | CACCTGTAATCCCAA[A/C]ACTTTGGGAAGCTGA | 7468 |
rs749350863 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939739 | AGCTCTTGGGTTTAG[C/T]AAAAGTTCATCTCCT | 7468 |
rs749392962 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942784 | TGTGGAAAATATCAG[C/T]GTCGCTACCCTCAGA | 7468 |
rs749405380 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884965 | AATACTAAAAATTAG[C/T]CAGGCGTGGTGGCGG | 7468 |
rs749440424 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906118 | TTACTGATTTCCTTT[C/T]TAGTGTCTGGGGATA | 7468 |
rs749497305 | in-del | -/TGC | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB, cds-indel | WHSC1 | GRCh38.p7 | 4:1899334 | GCCGCATAGCCCTGT[-/TGC]GCGGGCATCCTGTGC | 7468 |
rs749502189 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873393 | TAACATATAAACTAA[C/T]ATAACTTTTGGAGCC | 7468 |
rs749502820 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874089 | AGTAAATAATTAATC[A/G]GCAGCAACAGAAGCC | 7468 |
rs749516576 | in-del | -/C | 0.000149115 | 0.00863337 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978941 | GGCCGGATCCAGGGG[-/C]GGTGCAGGGCGGCCG | 7468 |
rs749523324 | snp | C/T | 1.65471e-05 | 0.00287633 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942314 | TAGAGCAAATTCTTA[C/T]TTTTTTCGCCTTCAC | 7468 |
rs749563121 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919063 | AGGATCCCTTGAGTC[C/G]TGGAGGCAGGAGGAT | 7468 |
rs749569581 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959177 | CTCTCTTCATCTTAC[A/G]ATGGCCTGGCTGGAT | 7468 |
rs749595883 | snp | A/G | 0.000197883 | 0.00994496 | missense | WHSC1 | GRCh38.p7 | 4:1900883 | CCCTTTATTCCAGCC[A/G]ACAAGCTGAAAGATC | 7468 |
rs749617066 | snp | C/G | 1.67835e-05 | 0.0028968 | missense | WHSC1 | GRCh38.p7 | 4:1956140 | ATGGAGGGGGACCGG[C/G]GCAGCCGCTACCAGG | 7468 |
rs749642783 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964106 | GGCTTTGCTTTTAGC[A/G]AGGACCTGAGGTAAC | 7468 |
rs749657140 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950518 | CCTGTGGTGTGAGTC[C/T]GGAAGACTCTCCTGA | 7468 |
rs749660877 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964879 | CTCAAAAAAGATCTG[G/T]AAAGACCTTAAATTT | 7468 |
rs749664227 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883839 | GGCGATAAGAAGCGA[G/T]TGTGGCCCACATGGA | 7468 |
rs749670640 | snp | A/C/T | 4.94616e-05 | 0.0049728 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974821 | TTTAAAAATAACATG[A/C/T]GATTGCTAACACTTG | 7468 |
rs749674511 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913819 | CAGCTGTCTTTTCTT[C/T]AATCTCTTTGTCTTG | 7468 |
rs749746437 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894533 | CAAAAATTAGCCAGT[G/T]TGGTGGTGCATGCCT | 7468 |
rs749761820 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944271 | TGGTTTCCTGAAGGA[G/T]GTGGGTGGAAACGGC | 7468 |
rs749800545 | snp | C/T | 8.8032e-05 | 0.00663387 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953184 | GCTTGGACTAGTGAG[C/T]AAGGTTGGAAACAGG | 7468 |
rs749802617 | snp | C/T | 3.29506e-05 | 0.00405884 | missense | WHSC1 | GRCh38.p7 | 4:1935221 | GAAGCTGAGGACACA[C/T]CCAGGAAAAGACTCA | 7468 |
rs749803296 | snp | A/G | 1.65952e-05 | 0.00288051 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957915 | AAAATCTTTACTCCT[A/G]TTTCATTGACTTTTT | 7468 |
rs749825396 | snp | C/G | 3.2962e-05 | 0.00405954 | missense | WHSC1 | GRCh38.p7 | 4:1900961 | CTGCGTTTTGAGTCC[C/G]AGGAAATGAAAGGGA | 7468 |
rs749840693 | snp | A/G | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982645 | GCCCTGGCCCACCCC[A/G]TCCTGATGGCCGCCT | 7468 |
rs749849043 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942411 | ACTTAGAATGATGTA[A/G]TATTCCAGGATGCTG | 7468 |
rs749851649 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977876 | CATGCCTCTAATCCC[A/G]GCACTTCTGAGAGGC | 7468 |
rs749854952 | snp | C/T | 1.67055e-05 | 0.00289006 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952247 | GCAAGTTCCCACGGG[C/T]GGGCAGCTCTGCAGC | 7468 |
rs749895097 | snp | C/G | 1.65072e-05 | 0.00287286 | missense | WHSC1 | GRCh38.p7 | 4:1918381 | GAAAACCCCAAGTCT[C/G]TGAGAGAAGAGTGCA | 7468 |
rs749980411 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974404 | TTTTTAGTAGAGATG[C/G]GGGTTCACCATGTTG | 7468 |
rs749989515 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941102 | GGAGCTTACTGAAAT[A/G]TGAAAAGGCAAATTT | 7468 |
rs749994357 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969984 | ACCACAAGAACGGCA[C/T]GAAGGTGGATGTGGG | 7468 |
rs750024530 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954540 | ATTTTTTTGTAGAGA[C/G]GAGGTCTCACTGTTG | 7468 |
rs750027038 | snp | C/T | 1.65701e-05 | 0.00287833 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952215 | AGGGAGGTTCACCTG[C/T]AGCGAGTGTGCCTCA | 7468 |
rs750031567 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977847 | AAAGAAAATCCAGGC[C/T]AGGCACGGTGGCTCA | 7468 |
rs750044677 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886752 | CTGAGGCAGGGTACT[C/T]GCTTGAACCTGGGGA | 7468 |
rs750069519 | snp | C/T | 1.67812e-05 | 0.0028966 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918506 | GGCAGAGGCTGACCC[C/T]AGAAGAGGAGTAGGG | 7468 |
rs750076380 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900939 | ACCCGGCGCACACGA[C/T]GCCAAACTGCGTTTT | 7468 |
rs750081326 | in-del | -/TGTGT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920488 | ATTATTGTGACTTAC[-/TGTGT]TGTGTAATGCTCATC | 7468 |
rs750083545 | snp | A/G | 8.37177e-05 | 0.0064693 | missense | WHSC1 | GRCh38.p7 | 4:1956129 | TGTTCCCGTACATGG[A/G]GGGGGACCGGGGCAG | 7468 |
rs750127826 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | WHSC1 | GRCh38.p7 | 4:1904310 | TGTGGTCCAAAGTGT[C/T]GGGTTACCCTTGGTG | 7468 |
rs750129561 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918839 | TAAAATATCCTTCCT[A/G]ATGTGGATAAGAAGA | 7468 |
rs750162968 | snp | C/T | 1.70043e-05 | 0.0029158 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952280 | GGCCGGCCACCTGCT[C/T]CTGCAACCCCCTGCA | 7468 |
rs750198137 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949606 | TCTCTACTAAAAATA[C/T]AAAAAATTTAGCCGG | 7468 |
rs750198438 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880112 | TTTTTGGTTAAAATA[-/TG]TGTTAGAAATAGGAG | 7468 |
rs750206042 | snp | C/T | 2.75145e-05 | 0.00370897 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976630 | TGACCGCAAGTTCTG[C/T]ACCAAGGCCTACCAC | 7468 |
rs750218606 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966520 | AAATTAGCCGGGCGT[A/G]GTGGCAGGCGCCTGT | 7468 |
rs750222558 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913574 | CTCTCTGAGAAATGC[A/G]TAGAAGAAATAATGT | 7468 |
rs750234085 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963555 | TGCCAAGTGGATACT[G/T]CAGTTTGCTTTTGAT | 7468 |
rs750256290 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964451 | GTTTCAGCTCTTGGC[A/G]CAGCAGCGGCTACCC | 7468 |
rs750259407 | in-del | -/T | 1.68105e-05 | 0.00289914 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904409 | GGTTGTTTTTCCAAC[-/T]TTCTCTTCTGCACTT | 7468 |
rs750267784 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951428 | TAGGATGAGATTTGT[A/G]TACACATCATGTAAT | 7468 |
rs750290666 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943514 | ACTGCATTATGCATG[C/T]GAGGATGAAATAAAC | 7468 |
rs750300039 | in-del | -/TTTTC | 8.02729e-05 | 0.00633483 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938408 | TTTCTTTTCTTTTTT[-/TTTTC]TTTCTTTTTTTTTTT | 7468 |
rs750322460 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953987 | GCTGATTTTTGTAAA[-/T]TTTTTTTTTTTTTGG | 7468 |
rs750322691 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881031 | ACTGATGAAATGGTA[A/C]ATCATCTAGGGTTTG | 7468 |
rs750325470 | snp | C/T | 1.65466e-05 | 0.00287628 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938486 | AACGGCCAGAACAAG[C/T]TCTTACAAGGCCATG | 7468 |
rs750333708 | snp | A/C | 1.64827e-05 | 0.00287073 | missense | WHSC1 | GRCh38.p7 | 4:1916951 | ATATTTGAGAAGAGC[A/C]TCGTAGCTTTTGAAG | 7468 |
rs750369321 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1893959 | TGATTGACAGACAGT[C/G]TTGCTCTGTAGCCCA | 7468 |
rs750378455 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926976 | TGTGGGCCAGGAATT[C/T]GGCAACCGCTTAGCT | 7468 |
rs750385663 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882170 | TGTTCAGGTGAAAAC[C/T]TTTCCTTTGTCCCTG | 7468 |
rs750399890 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911182 | GGAACACAGTACAAA[A/G]TTAGGTACCAGGACT | 7468 |
rs750429483 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875886 | TGCACTCCAGCCTGG[C/G]AGACAGCGAGACTCC | 7468 |
rs750432098 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975761 | CCTTGGCTTGTAGCA[A/G]CACCGCCCAACCATT | 7468 |
rs750438963 | snp | C/T | 1.6836e-05 | 0.00290133 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961003 | ATTGGTCAGCACGCT[C/T]TTTGTCATGGCCACA | 7468 |
rs750474771 | snp | G/T | 1.91261e-05 | 0.00309236 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974594 | CTTGTTTGCCATCAT[G/T]GAGGATGCTGGGAGC | 7468 |
rs750479519 | snp | A/G | 3.29962e-05 | 0.00406165 | missense | WHSC1 | GRCh38.p7 | 4:1961116 | CACGCACACGAGAAC[A/G]ACATCACCCACTTCT | 7468 |
rs750487141 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878473 | CTTAGATTTTCTCCA[G/T]AGCACATACCTCCAA | 7468 |
rs750489573 | snp | C/G | 3.92819e-05 | 0.00443164 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955360 | GGGGCCTGGGGGTGT[C/G]TGCGGCACACGCCTC | 7468 |
rs750496613 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959112 | CAGAAGAGCTCTTAC[C/G]AGCGTTTGCTGGACA | 7468 |
rs750506246 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923192 | TAAAACTATGTATGT[A/T]AAAATGAAAATCTAG | 7468 |
rs750511963 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904586 | TCTGATTGAATTAGT[A/G]TTAAGGGACACATGA | 7468 |
rs750552239 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908816 | TCTTGGCTCTGTTGC[C/T]CTGTCCAGGCTAGAG | 7468 |
rs750589697 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924983 | CACTCTGCCCTGCCC[A/G]CCCCTGGTTCCTGAT | 7468 |
rs750610168 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937159 | TCGATTCAAGTGATT[C/G]TCCTGCCTCAGACTC | 7468 |
rs750651391 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891731 | CGTGGTGGTCGGCAC[-/CT]CTGTAGTTCCAGCTA | 7468 |
rs750660030 | snp | A/C | 1.81368e-05 | 0.00301132 | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1900630 | TAATACCATAGTGTT[A/C]TAAGAACGGAAGCAT | 7468 |
rs750667217 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951164 | CTCATCCAAAAAGTC[C/T]GAGCGAGGAGTGACT | 7468 |
rs750668483 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892005 | TTTCTCTTTTCCTAG[C/G]ATATCTACTCTTCCT | 7468 |
rs750683813 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877165 | AAATTGTTATGCTTT[A/T]AGAGGATCTGTGCAT | 7468 |
rs750692055 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972743 | AAACCGAAAACGCAT[A/G]AAGCAAAAGGGTAAA | 7468 |
rs750698924 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981497 | GATTCCTTGGCATCC[A/G]AAACCAGCATCTGCA | 7468 |
rs750699195 | snp | A/G | 1.65913e-05 | 0.00288017 | missense | WHSC1 | GRCh38.p7 | 4:1930660 | ATGCTTCAGGTGAGG[A/G]GATTGAAGAGCTGCT | 7468 |
rs750722330 | snp | C/T | 1.64928e-05 | 0.00287161 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951085 | AGGTCTCGGACAGCC[C/T]GGGAGACGAGCCCTC | 7468 |
rs750733241 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975322 | TTTTAACTACAACCT[C/T]GATTGTCTGGGCAAT | 7468 |
rs750735104 | in-del | -/AA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967183 | TAACTGAGATGAAAT[-/AA]AGACAAATTCCTAGA | 7468 |
rs750743087 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901343 | GAGTACTGGGGCGGG[C/T]GGAGAAGGTGAGGAC | 7468 |
rs750753436 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925881 | ATCATGGCTTGCCAC[A/G]GCCTTGACCTCCCTA | 7468 |
rs750788107 | snp | A/C/G | 4.96622e-05 | 0.00498287 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975042 | ATGGGGCTCCTGGCT[A/C/G]TGGGGGCAGAGTGGC | 7468 |
rs750862088 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958594 | GCCGCATCCCCAGGA[C/G]CCTCGTGGCCGTTCC | 7468 |
rs750870676 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931618 | CACCTAAAGGGAAGT[A/C]GGGGCCCAGAAGCGA | 7468 |
rs750888027 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916507 | CACACCACCACACCC[A/G]GCTAATTTTTGCATT | 7468 |
rs750922691 | snp | C/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870297 | TGACCAAACTCTCGC[C/G]AGGCTCCCCTGGGCC | 7468 |
rs750923496 | snp | C/T | 3.36247e-05 | 0.00410015 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904207 | TTGTCTTCTGTTGTT[C/T]ATTTTCAGATTCCAG | 7468 |
rs750927886 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953441 | ACCCTCTGACTGTAT[C/T]TGAGAGCCGAGGTTT | 7468 |
rs750964285 | snp | A/G | 1.65157e-05 | 0.0028736 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959506 | AGTCCAGATCTACAC[A/G]GCGGATATTTCAGAA | 7468 |
rs750966891 | snp | A/G | 1.71693e-05 | 0.00292991 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930814 | TGCTTGGGTTGATGT[A/G]TGTAGTGTAGCAAGC | 7468 |
rs750981403 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882302 | GAAGCGCTGAGACAC[A/G]TGCTTTATCGTGTTC | 7468 |
rs750985858 | in-del | -/TAG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921852 | ACGTTGTACGGAAAA[-/TAG]TAGCCAATATTAGGC | 7468 |
rs750985960 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961454 | ACACAGATGAGGAAG[C/T]CTCAGCATCTTCTTT | 7468 |
rs751014140 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943885 | CATGATGAATTTTGC[A/G]TGGGTGGCCAGCCAG | 7468 |
rs751018529 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975805 | TGACTGTTGACTTGC[C/G]CTTCTTATAAGAGCA | 7468 |
rs751095741 | snp | A/T | 3.29468e-05 | 0.00405861 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974868 | GACCTTACAGGACCG[A/T]ATAATAGACGCTGGC | 7468 |
rs751112192 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977659 | CATGCACCTGTAATC[A/C]CAGCTATTCGGGAGG | 7468 |
rs751123157 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921327 | AGCTGGGCATGGTGG[C/T]GTGCGCCTGTACTTC | 7468 |
rs751133188 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957195 | ACGGATTGTAGGGGT[A/G]TGTGTTTCCTCGGTT | 7468 |
rs751134237 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927136 | GAGGCCTCGGTCCTT[C/T]ACCATGTGGCCCTCT | 7468 |
rs751138696 | snp | A/G | 6.59283e-05 | 0.00574106 | missense | WHSC1 | GRCh38.p7 | 4:1900950 | ACGATGCCAAACTGC[A/G]TTTTGAGTCCCAGGA | 7468 |
rs751170241 | snp | A/G | 3.32707e-05 | 0.00407851 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935308 | CAGAGTGTATGCTCT[A/G]TGACTCTTGGTGCCA | 7468 |
rs751242322 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905574 | CAAAACAGGCTTGTC[A/C]GCTGGCTGTGGGAGC | 7468 |
rs751258620 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894157 | AGACGGCGTCTTACT[A/G]TGTTGGCCAGGCTGG | 7468 |
rs751270923 | in-del | -/TGTC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978498 | CTGTGGTAGACAGTT[-/TGTC]TGCCCGTCCTGTTCG | 7468 |
rs751282562 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965891 | CCCATAATCCAGTCA[C/G]TTCCCACCAGGTTCC | 7468 |
rs751291331 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928209 | GTCCAGCTTGTTTTT[-/T]GATATGTTAAGAATA | 7468 |
rs751306053 | snp | A/G | 1.64972e-05 | 0.00287199 | missense | WHSC1 | GRCh38.p7 | 4:1978713 | GCCACCTCTGCCCCA[A/G]TTCGTTCTGTAAGGA | 7468 |
rs751307295 | snp | C/T | 1.656e-05 | 0.00287745 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958054 | GGCGTGTGGGAGCTG[C/T]GTGCACGCGTGTGGA | 7468 |
rs751314482 | snp | A/C | 1.65304e-05 | 0.00287488 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938494 | GAACAAGCTCTTACA[A/C]GGCCATGGAGGCAGC | 7468 |
rs751318500 | snp | A/G | 3.32082e-05 | 0.00407468 | missense | WHSC1 | GRCh38.p7 | 4:1961143 | TTCTACATGCTCACT[A/G]TAGACAAGGTAATGC | 7468 |
rs751335429 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980766 | ACTTGCTCGCGCGGC[C/T]GTGGCCTCTGAGGGG | 7468 |
rs751359183 | snp | C/T | 1.74464e-05 | 0.00295345 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978622 | CTGTGTGCTCACATC[C/T]TGTGTTCTGTTGCAG | 7468 |
rs751396867 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978439 | CCTTAGGGGCCTGGC[A/G]GGTACTGTGGAGTCA | 7468 |
rs751434668 | in-del | -/A | 1.69781e-05 | 0.00291355 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952062 | TGGTAAGAGGTGCAG[-/A]AAGGGACTGCCGGGC | 7468 |
rs751436883 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913723 | GCCCCCTTGCCTTGT[A/C]TACAATAAATAACAG | 7468 |
rs751471755 | snp | A/G | 1.80286e-05 | 0.00300233 | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1900638 | TAGTGTTCTAAGAAC[A/G]GAAGCATCTGGGCTG | 7468 |
rs751511091 | in-del | -/ACA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873413 | CTTTTGGAGCCATGC[-/ACA]ACAAAATTATAAGGT | 7468 |
rs751520729 | in-del | -/TC | 0.00101582 | 0.022514 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938411 | CTTTTCTTTTTTTTT[-/TC]TTTCTTTTTTTTTTT | 7468 |
rs751528522 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914311 | TACATGTGTGAGCCA[C/T]TGCACCCAGCCCAGA | 7468 |
rs751543597 | snp | C/T | 1.81602e-05 | 0.00301326 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918094 | AAAAGTAGTTAACTT[C/T]TATGTTTGTGTAGTG | 7468 |
rs751563331 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905221 | GAGGAATAGTAAAAG[A/G]TAATGTGGTTTGAGG | 7468 |
rs751565534 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947522 | CTAGAAGGGTCACTT[C/T]AATAAAAATTGTTAT | 7468 |
rs751608776 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961817 | TCCCTTCCCTCACAC[A/G]GCAGGCTTTTGGCTT | 7468 |
rs751699153 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948519 | CATTGGATCCTCCCC[A/G]ACTGTGGCTAGTTGT | 7468 |
rs751704964 | snp | C/T | 3.30284e-05 | 0.00406363 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900738 | GGCACCAGAAATCCT[C/T]GGCAGTGCCAACGGG | 7468 |
rs751728783 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878765 | TGGGCTGGTGGCAGA[C/G]GTCACAGAAGAGCCT | 7468 |
rs751730978 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910751 | TATTACTTGCTGAGA[A/G]ATGTGTTAAAATCTC | 7468 |
rs751733456 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960631 | CACCTCCCCAGCACC[C/T]TTGTTCCTCGCCTGC | 7468 |
rs751736225 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970722 | TGGGCTCTAGGGGCG[G/T]TTGAGGGAGGGGGTC | 7468 |
rs751737438 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909638 | CCTCTATTCCTATCC[-/T]TTTTTTTTTTTCTTT | 7468 |
rs751742931 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955563 | TGCTCTCGTGCTGAT[-/G]GTACAGATCGCTGTT | 7468 |
rs751758497 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974117 | GGTGCAAAGTCAGAG[C/T]TCACTGTCACTCGGA | 7468 |
rs751780483 | snp | A/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892802 | TTGAACTCCTGACCT[A/T]GTGATCCGCTCGCCT | 7468 |
rs751804575 | snp | A/G | 1.72713e-05 | 0.0029386 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930821 | GTTGATGTGTGTAGT[A/G]TAGCAAGCTGAGCTC | 7468 |
rs751874982 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | WHSC1 | GRCh38.p7 | 4:1975353 | GAAAAAACGGTCTGC[C/T]GGTGTGGAGCCTCCA | 7468 |
rs751878561 | snp | C/G | 1.65397e-05 | 0.00287569 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953466 | AGGTTTCCGCTGCCC[C/G]CTCCACAGCTGTGTG | 7468 |
rs751878995 | snp | A/C | 1.64768e-05 | 0.00287021 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959713 | TGGCAAAGGGTGGGG[A/C]CTGGTCGCCAAGAGG | 7468 |
rs751882425 | snp | C/G | 5.02904e-05 | 0.00501425 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976452 | ATTCTTTCCGGTGAT[C/G]TGTGCTTAATTCTTG | 7468 |
rs751887985 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934381 | TGAGCCACCATGCCC[A/G]GCCTAGGAAAAGATT | 7468 |
rs751925120 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904248 | GTCTTGTCCAAACAC[C/T]GGAAGAGACAAAGAC | 7468 |
rs751934125 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959518 | CACAGCGGATATTTC[A/G]GAAATCCCTAAGTGC | 7468 |
rs751969424 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956267 | TATTTTTTAAAATTT[A/G]ATCTTTATAGAAAAT | 7468 |
rs751988090 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971034 | CTCTGCAGCATGCAA[A/G]GAACAAAGAGATTCT | 7468 |
rs751993636 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918924 | AGGCCAAGGCGGGAG[A/G]ATTGCTTCAGCTCAG | 7468 |
rs751997252 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949450 | AGTCACCAGTCAGAG[A/G]CGACGGAAGCCCTTG | 7468 |
rs751999035 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898360 | CCAAAGCCTGACCAC[A/G]TTCCCCTTAAAAATG | 7468 |
rs752015412 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886959 | CCCCTCTTACCTCCC[A/G]TGTTACCTCCCTTCT | 7468 |
rs752037034 | in-del | -/C | 0.000184089 | 0.00959222 | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1978831 | ACCAAGACTGAGAAG[-/C]CCCCCCCCAGAGCCA | 7468 |
rs752059206 | snp | A/T | 1.65012e-05 | 0.00287234 | missense | WHSC1 | GRCh38.p7 | 4:1955197 | GCTGCCCCGTTGCCT[A/T]TCACAGCGGGGATGC | 7468 |
rs752084783 | snp | C/T | 0.000100118 | 0.00707455 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959485 | GGTGAATAAGCCTTA[C/T]GGGAAAGTCCAGATC | 7468 |
rs752099397 | snp | G/T | 1.65211e-05 | 0.00287407 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939812 | CGATAACCATGGCAT[G/T]GGTATGAAGGCCATT | 7468 |
rs752113048 | snp | C/T | 6.6599e-05 | 0.00577019 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904382 | CCAAACTTAAAGGTA[C/T]TGTGTTCTTTGGGTT | 7468 |
rs752121654 | in-del | -/TCGCGGTGGCTTGCAGCT | 1.76058e-05 | 0.00296692 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976694 | GGTGGGTGTGCAGCC[-/TCGCGGTGGCTTGCAGCT]GTGTCTGTGTGGCAG | 7468 |
rs752145888 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964638 | GTGCGCTGCGCTGCC[C/G]TTGTTATCACACCTC | 7468 |
rs752161799 | snp | A/G | | | missense | WHSC1 | GRCh38.p7 | 4:1978862 | GGGAAGCCGAAGGGG[A/G]AGAGGCGGCGGCGGA | 7468 |
rs752188446 | snp | G/T | 1.89561e-05 | 0.00307858 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953260 | GATTTTAGTGGCTCA[G/T]AACTGCAATTTAATT | 7468 |
rs752188754 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914579 | GATCTGCCCACCTTG[A/G]CCTCCCGAAGTGCTG | 7468 |
rs752206765 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977541 | GTACTTTGGGAGGCC[-/A]AAGGTGAGCAGATCA | 7468 |
rs752231243 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920767 | GGCCGAGTGTGGCAG[C/T]TCACACCTGTCATCC | 7468 |
rs752263356 | snp | C/T | 1.78848e-05 | 0.00299033 | missense | WHSC1 | GRCh38.p7 | 4:1901238 | CTAAGATCTCAAGTC[C/T]TTCAGATAAAAAGGT | 7468 |
rs752267702 | in-del | -/GTGAATACTGCCTGCCGTCAGCGTGGCACCTGCCATCTGGATTAGG | 1.65847e-05 | 0.0028796 | frameshift-variant, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952222 | TCACCTGCAGCGAGT[lengthTooLong]GTGCCTCAGGCAAGT | 7468 |
rs752315540 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928784 | CCGTGAAGGAATGTG[C/T]TGTGTTTGAGGAGGT | 7468 |
rs752331666 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945449 | TGGGTCTGTCACAGA[C/G]AAGTTTAAAAAAGAA | 7468 |
rs752348506 | snp | C/G | 1.64999e-05 | 0.00287222 | missense | WHSC1 | GRCh38.p7 | 4:1978735 | CTGTAAGGAGCACCA[C/G]GACGGGACAGCCTTC | 7468 |
rs752370406 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968971 | AATGTACACAAAGTA[-/C]ATCTTCACTGAAACT | 7468 |
rs752377919 | in-del | -/TGTG/TGTGTGTGTGTG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872564 | AGATAACGTGTATTT[-/TGTG/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 7468 |
rs752396637 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976766 | TCTTCCTGCTGACCG[C/G]GCCTCATCTGGGTGC | 7468 |
rs752399555 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902064 | CTTGATGGGGCAGCA[A/G]TCTCTGTTCATCTGG | 7468 |
rs752421548 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953415 | TTACCATGAGGCTTG[C/T]GTGAAAAAATACCCT | 7468 |
rs752421655 | snp | A/C | 1.65252e-05 | 0.00287443 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938498 | AAGCTCTTACAAGGC[A/C]ATGGAGGCAGCCTCC | 7468 |
rs752451870 | snp | A/G | 1.78102e-05 | 0.00298409 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974673 | CTCCACGTGGTCCTG[A/G]CCTGTCCTCTGTGAG | 7468 |
rs752461931 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945226 | ACTGGGGAACAAGAC[A/G]GGGTGGGGTGGGGAG | 7468 |
rs752501743 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939333 | GAGATTTGTGCTAAA[C/T]TTCTTATGGATGAAA | 7468 |
rs752502777 | snp | A/T | 7.60529e-05 | 0.00616609 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974616 | GCTGGGAGCTCCAGC[A/T]CCCTGTCCTGTCCTC | 7468 |
rs752539028 | snp | G/T | 1.65839e-05 | 0.00287953 | missense | WHSC1 | GRCh38.p7 | 4:1978789 | CTACTGCTGTGAGCA[G/T]GACTTAGGGGCGGCA | 7468 |
rs752547407 | snp | C/T | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982327 | TCATTTTGCCTTTGA[C/T]CTGACCCGCTGGGGA | 7468 |
rs752556934 | snp | A/G | 1.64898e-05 | 0.00287135 | missense | WHSC1 | GRCh38.p7 | 4:1900857 | AGAAGTTTAACGGCC[A/G]CGACGCCCTGCCCTT | 7468 |
rs752561839 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973715 | AGTTGTGTCAGAGGC[C/T]GCGTGTGAATAGTGA | 7468 |
rs752573258 | snp | A/G | 3.39328e-05 | 0.00411889 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952067 | AAGAGGTGCAGAAGG[A/G]ACTGCCGGGCGCTGC | 7468 |
rs752576102 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901350 | GGGGCGGGCGGAGAA[A/G]GTGAGGACAGGCCTG | 7468 |
rs752594374 | snp | A/T | 1.65575e-05 | 0.00287724 | missense | WHSC1 | GRCh38.p7 | 4:1918256 | AGTTCACCTTTCTCT[A/T]TGTGGGGGACCAGCT | 7468 |
rs752608193 | snp | C/T | 1.65083e-05 | 0.00287296 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918371 | AGAAGCTGCTGAAAA[C/T]CCCAAGTCTGTGAGA | 7468 |
rs752642008 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885808 | TAGTTCCTCACTGCT[C/G]TCTTCCCTCAGGACA | 7468 |
rs752663390 | snp | C/T | 1.72791e-05 | 0.00293926 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935113 | TTTTGGAGTGGTTTT[C/T]ATGTACATTTTCCCC | 7468 |
rs752664078 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902642 | CAGGGTCTTGGTATG[C/T]TGCACAGGCTGTTCA | 7468 |
rs752692981 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940438 | ACATGACACTTAGAC[-/TT]TATTATCAAACCTAA | 7468 |
rs752739417 | in-del | -/AAT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964960 | AGAACAATAAATAAA[-/AAT]AACAAAAACAGCAAA | 7468 |
rs752766057 | snp | C/T | 1.65414e-05 | 0.00287583 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952164 | CTGCTGCGGAGCTTT[C/T]CACCTCGCCTGCCTT | 7468 |
rs752790209 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949491 | ACTCTGGCTGGGTGC[A/G]GTGGCTCATGCCTGT | 7468 |
rs752810923 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979010 | GAGGACCCAGCTCGA[A/G]CCGCCAGGACACAGA | 7468 |
rs752851097 | snp | C/T | 1.68858e-05 | 0.00290561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1960989 | CCCCGACACTGAGGA[C/T]TGGTCAGCACGCTTT | 7468 |
rs752867832 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879441 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 7468 |
rs752874197 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887267 | TGAGGGAGGAAGTGA[A/G]ATCTGCCAGTCGTTT | 7468 |
rs752876397 | in-del | -/GTAAA | 5.09719e-05 | 0.0050481 | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1900700 | TCTGTTCAGAGTGTT[-/GTAAA]GTGCATAAAGATGAA | 7468 |
rs752884987 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881847 | GGGATAGACACTAGA[A/G]CAGGGAGCAGAGAGC | 7468 |
rs752913010 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963376 | CCTGGGAGGGTTTTA[C/G]CCCTAGGGAAGGGAC | 7468 |
rs752941320 | snp | A/G | 3.29843e-05 | 0.00406092 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955225 | TGCTTGTCTGGCAGC[A/G]GGATGCTCAGTGATC | 7468 |
rs752944788 | snp | C/T | 1.68131e-05 | 0.00289935 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904411 | TTGTTTTTCCAACTT[C/T]CTCTTCTGCACTTAA | 7468 |
rs752946171 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978505 | AGACAGTTTGTCTGC[C/T]CGTCCTGTTCGCTGG | 7468 |
rs752975157 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880613 | TGAAATACTCCTGCC[-/A]AAAAAAAAAAAAATC | 7468 |
rs752997781 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904257 | AAACACTGGAAGAGA[C/T]AAAGACCACCTGTTG | 7468 |
rs753003857 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913371 | AGAAGACTCTGCTCC[A/G]CCACCTCTTGTGGAA | 7468 |
rs753037937 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876608 | GAAGTGGGAGGTCAC[C/T]TGAGTCCAGGACTTT | 7468 |
rs753078585 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972385 | AAAATAGCAAAAACG[A/T]TTAAATATACCTGGA | 7468 |
rs753083791 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957622 | CTGTCTGAGAACAGC[A/G]AGTCCCAGGCTTTGA | 7468 |
rs753092631 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894988 | TCTACTTCCTGTCTC[-/T]TATGTATTCTATTCT | 7468 |
rs753098556 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971276 | GGCAGAATTCAGGCC[C/T]TACCACTTTCAGTGA | 7468 |
rs753120179 | snp | A/G | 0.000212153 | 0.0102972 | missense | WHSC1 | GRCh38.p7 | 4:1900665 | GCTGGATGGAATTTA[A/G]CATCAAGCAGAGTCC | 7468 |
rs753134332 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935553 | TTTTAGATTGGACAA[A/G]ATTGTCACTAAAAAT | 7468 |
rs753136559 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919295 | TCCAGCAGTCTGTTC[A/T]GAAGCTTCCAGTGCA | 7468 |
rs753141634 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888688 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGATT | 7468 |
rs753146221 | snp | C/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906986 | TTCTTTGCTTGACTC[C/G/T]GGGACCTTGCACTGT | 7468 |
rs753165840 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874821 | ATGGGGGCTTTAGAG[G/T]ATTAGGCTTGTATTT | 7468 |
rs753168018 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905941 | CTGTCTCCCCTTTGT[C/T]TGAGGATGGACCTTC | 7468 |
rs753173456 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943948 | AGCCAGCGCATAGGT[A/G]CTCCCTCTATATTAT | 7468 |
rs753201061 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933859 | CGTCTTAGGTTGATA[C/T]TGTTTGGATGCCTTA | 7468 |
rs753219330 | snp | G/T | 1.78159e-05 | 0.00298457 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953555 | CGCAGCCTTGCTGTG[G/T]GTTCAGATGCAGGCC | 7468 |
rs753226426 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921052 | TAAACAAAAAAATTA[C/T]TGCTTATTGATAAAA | 7468 |
rs753228372 | snp | C/T | 3.29826e-05 | 0.00406082 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942437 | TGCTGCTGCAGGTGG[C/T]GTATCATCGTACACA | 7468 |
rs753299316 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981653 | GGCCGGCCTTTCTTC[C/T]GGCGACACCCGTCCA | 7468 |
rs753305456 | snp | C/G | 3.05712e-05 | 0.00390956 | missense | WHSC1 | GRCh38.p7 | 4:1978881 | GGCGGCGGCGGAGGG[C/G]CTGGCGGAGAGTCAC | 7468 |
rs753322430 | snp | G/T | 6.70297e-05 | 0.00578882 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974793 | AATGTGCTTTATGAT[G/T]GTGAAAATTCCCTTT | 7468 |
rs753339268 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968007 | TCTGGGAGAGAAATT[A/G]GGCCAGGTTCAAGTG | 7468 |
rs753357767 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954398 | GACAGGGTCTCCTTC[C/T]GTTGCTCAAGCTAGA | 7468 |
rs753360836 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913225 | GCTCCTTGGACTAGC[G/T]GTAACGCCAGTGCCT | 7468 |
rs753363436 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954450 | TCACTGTAGCCTTGA[C/T]CTCCCAGGCTCAGGT | 7468 |
rs753418501 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981664 | CTTCCGGCGACACCC[A/G]TCCATGGCTGGCTGG | 7468 |
rs753443319 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966465 | ATCGAGATCATCCTG[C/G]TTAACACGGTGAAAC | 7468 |
rs753446032 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885843 | CCAGGCGCAGGAATG[A/G]TATAGAAAAACTGAG | 7468 |
rs753458271 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916211 | AGGTTGTGTGATGTC[C/T]GTATACTGCCTCCTT | 7468 |
rs753462758 | in-del | -/T | 5.24104e-05 | 0.00511884 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978621 | CTGTGTGCTCACATC[-/T]TTGTGTTCTGTTGCA | 7468 |
rs753476898 | snp | A/G | 1.76418e-05 | 0.00296995 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974694 | CCTCTGTGAGCAAGA[A/G]AAACAGGACTGGTTT | 7468 |
rs753512534 | snp | C/G/T | 4.95244e-05 | 0.00497596 | missense | WHSC1 | GRCh38.p7 | 4:1918377 | TGCTGAAAACCCCAA[C/G/T]TCTGTGAGAGAAGAG | 7468 |
rs753524447 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884751 | ATTGGGATTATATAT[C/T]GTGTTAACAGTTTAT | 7468 |
rs753531668 | in-del | -/GGAGCTCC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922716 | GATCACCGGAGGTCA[-/GGAGCTCC]GGAGCTCCAGACTAG | 7468 |
rs753591762 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962019 | TAGAAAATGATCACC[A/G]ATAAAAAAATGTTGA | 7468 |
rs753598404 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951653 | CCACAGGACCCCAGC[C/T]AGGCCACCTACACTC | 7468 |
rs753604188 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935032 | CAGGGTTACAGGAAA[C/T]CCATCATGGGCTGGA | 7468 |
rs753644352 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925264 | AACCCTTGAGGGATA[C/G]AGTCAGGTGGAACTT | 7468 |
rs753660550 | in-del | -/T | 1.83586e-05 | 0.00302968 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901266 | GGTATTTAGGAGACG[-/T]TGTGTAAGGGGTCAT | 7468 |
rs753675731 | snp | A/G | 1.70081e-05 | 0.00291612 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974763 | TTTCAGTACAACAAG[A/G]AACACAACTTGTTCA | 7468 |
rs753687101 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975554 | GGCTGGGGAGGATGG[C/G]TCTCAACAAAGGCCA | 7468 |
rs753713443 | snp | A/C | 1.64923e-05 | 0.00287156 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935175 | AAAAAGAAACCACAC[A/C]AAGAGGATACAGGAC | 7468 |
rs753748334 | snp | A/G | 1.64925e-05 | 0.00287158 | missense | WHSC1 | GRCh38.p7 | 4:1900862 | TTTAACGGCCACGAC[A/G]CCCTGCCCTTTATTC | 7468 |
rs753763697 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892281 | GTGAGCCCCCACACC[C/T]GGCCTGAGTGAGTGG | 7468 |
rs753781706 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892888 | CACTGGTAACTCTTA[A/G]CTGGTAATTTTTGTT | 7468 |
rs753803388 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904161 | TCCTTGGTCTTCTGG[A/G]TACACAGGTAGTGAT | 7468 |
rs753820897 | snp | A/G | 1.65455e-05 | 0.00287619 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952197 | GCTTTCCCGGAGGCC[A/G]GAAGGGAGGTTCACC | 7468 |
rs753834990 | snp | C/T | 6.59478e-05 | 0.00574191 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900930 | TAATGGAGAACCCGG[C/T]GCACACGATGCCAAA | 7468 |
rs753855776 | snp | C/T | 1.65086e-05 | 0.00287298 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935267 | GTCTTCGGAAGGTAA[C/T]TGTGTTCCAGGTTTG | 7468 |
rs753863469 | snp | C/T | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982571 | GTCAAGGGAGTACCC[C/T]GAGGGCTGATCCTAC | 7468 |
rs753865108 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972552 | GGGCCCAAACCCAGG[C/T]GGATGGCCAGGGGGA | 7468 |
rs753920669 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890892 | GTAAGCCACCACGCC[C/T]GGCCTTTTTTTTCTT | 7468 |
rs753928403 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936794 | AAAGAATGGAAAATA[C/T]ATCTCACATATTGCT | 7468 |
rs753936309 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971562 | GAAATAAATAAATCT[C/T]TTCTTACGAGCCCAC | 7468 |
rs753982840 | snp | C/T | 0.000113439 | 0.00753039 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976597 | CCGCTGCGGTGATGG[C/T]GGGCAGCTGGTGCTG | 7468 |
rs753988522 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921159 | TTACACATGAAACTT[C/T]AGAAGCATTCTCCTT | 7468 |
rs753991298 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899613 | GTGTACTCCTGAGAG[A/G]TGCCTTCCCAGCTGG | 7468 |
rs754004432 | snp | C/T | | | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975201 | CAGATACAAAAATAA[C/T]AAGAGTATTTTTGTT | 7468 |
rs754009089 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908748 | GACCTGTGGGCTGTG[-/CT]TGTAGTCTGTCCCAA | 7468 |
rs754086406 | snp | C/T | 1.64977e-05 | 0.00287203 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942445 | CAGGTGGCGTATCAT[C/T]GTACACACTCAGTGA | 7468 |
rs754090627 | snp | G/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870589 | CACGCAGTCGCCCGC[G/T]CCACCCCCTGAAGCC | 7468 |
rs754103431 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974895 | TGGCCCCAAAGGAAA[C/T]TACTCTCGATTTATG | 7468 |
rs754112437 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979843 | GCCCTGAGCTCCATG[A/G]CGAAAGGAGTGACTT | 7468 |
rs754123039 | snp | G/T | 1.64819e-05 | 0.00287066 | missense | WHSC1 | GRCh38.p7 | 4:1916930 | GACGCCCCAGAAAGA[G/T]CTTGGATATTTGAGA | 7468 |
rs754150618 | snp | A/C/T | 3.29828e-05 | 0.00406085 | missense, synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961109 | AATCAAGCACGCACA[A/C/T]GAGAACGACATCACC | 7468 |
rs754194889 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960019 | GCGTGTTTGACCATG[C/T]CCTAATAATTTTATT | 7468 |
rs754212766 | snp | A/G | 3.59796e-05 | 0.00424129 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978891 | GAGGGGCTGGCGGAG[A/G]GTCACAGAGGGCAAA | 7468 |
rs754225949 | snp | A/T | 1.82864e-05 | 0.00302372 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900618 | TTTTCTTTTTTTTAA[A/T]ACCATAGTGTTCTAA | 7468 |
rs754237782 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977356 | TGACTCTGGCGGTGC[A/G]CAGACATCATGGCTC | 7468 |
rs754254680 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961001 | GATTGGTCAGCACGC[-/T]TTTTTGTCATGGCCA | 7468 |
rs754290065 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906991 | TGCTTGACTCCGGGA[C/T]CTTGCACTGTGGCTA | 7468 |
rs754290126 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922358 | CAAAATGTCAGGTAC[C/T]GCGGAATCAATATTA | 7468 |
rs754310312 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929350 | TGGTAATGGTAACCA[A/T]CCAACATTAACCTGA | 7468 |
rs754312877 | snp | C/T | 3.41408e-05 | 0.00413149 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930623 | CTTCTCCCGTTCCCA[C/T]AGGTGGTAGCTGAGC | 7468 |
rs754314502 | snp | A/G | 1.64936e-05 | 0.00287168 | missense | WHSC1 | GRCh38.p7 | 4:1901117 | GATGTGTCTCAGTCA[A/G]AAGAAAATGGACAAA | 7468 |
rs754315448 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965614 | TACATGCAAGGTGTA[G/T]TAGTCTATTTTTACA | 7468 |
rs754360203 | snp | C/T | 4.96882e-05 | 0.00498414 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958058 | TGTGGGAGCTGCGTG[C/T]ACGCGTGTGGAGGGA | 7468 |
rs754365798 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918672 | TTCAGAATTTGAGGA[A/G]CATCCCTTCAGTGCA | 7468 |
rs754377921 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908612 | GAGAAGTGAGGGAAG[C/G]ACAGAGTGCTAGTCA | 7468 |
rs754405808 | snp | C/T | | | missense | WHSC1 | GRCh38.p7 | 4:1976527 | AGACCAAGAAGAAAA[C/T]GAGGCGGCGCAGAGC | 7468 |
rs754438218 | in-del | -/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882379 | GGCAAGAAAGAAAAC[-/TT]TGGGCTGGGCTTAGT | 7468 |
rs754442941 | in-del | -/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932356 | AGGCACGAGAATCTC[-/TT]GAACCCGGGAGGCAG | 7468 |
rs754447802 | in-del | -/CTTTC | 0.00109563 | 0.0233798 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938412 | TTTTCTTTTTTTTTT[-/CTTTC]TTTTTTTTTTTTTTT | 7468 |
rs754460633 | snp | A/T | 0.00011537 | 0.00759418 | missense | WHSC1 | GRCh38.p7 | 4:1900958 | AAACTGCGTTTTGAG[A/T]CCCAGGAAATGAAAG | 7468 |
rs754462902 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880891 | GAATATCATTTGTGA[G/T]ATTTGAGACAGAATT | 7468 |
rs754468750 | snp | C/T | 6.59674e-05 | 0.00574277 | missense | WHSC1 | GRCh38.p7 | 4:1901106 | ACAGTGCTGCTGATG[C/T]GTCTCAGTCAGAAGA | 7468 |
rs754495275 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927138 | GGCCTCGGTCCTTCA[C/G]CATGTGGCCCTCTCC | 7468 |
rs754502197 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913264 | ACCTGTTACTTAGCC[A/G]ACCTTGGTCTAGCGG | 7468 |
rs754559424 | snp | C/T | 3.34874e-05 | 0.00409177 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957904 | CTGTATTTACTAAAA[C/T]CTTTACTCCTATTTC | 7468 |
rs754651448 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951749 | ATGCATGGGAAGTGT[A/G]AATACTGCCTGCCGT | 7468 |
rs754657745 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909959 | TAAAAAAAAAAAAAA[A/T]TATTTATCATGCTTG | 7468 |
rs754672453 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975806 | GACTGTTGACTTGCC[C/T]TTCTTATAAGAGCAC | 7468 |
rs754679462 | snp | A/G | 1.81632e-05 | 0.00301351 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918098 | GTAGTTAACTTTTAT[A/G]TTTGTGTAGTGAAAC | 7468 |
rs754695728 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889251 | ACTCAGGCTGGAGTG[C/T]AGTGGTGTAATTATG | 7468 |
rs754703134 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943939 | TTAGAAGTCAGCCAG[C/T]GCATAGGTGCTCCCT | 7468 |
rs754719706 | snp | G/T | 1.6625e-05 | 0.00288309 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935313 | TGTATGCTCTGTGAC[G/T]CTTGGTGCCACTGTT | 7468 |
rs754730582 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939981 | ATTTGAGCACTTTTT[A/G]TACACACGCACACAG | 7468 |
rs754736806 | snp | A/G | 1.65299e-05 | 0.00287483 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938495 | AACAAGCTCTTACAA[A/G]GCCATGGAGGCAGCC | 7468 |
rs754739342 | snp | C/T | 6.12339e-05 | 0.00553292 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953253 | GTTGCTTGATTTTAG[C/T]GGCTCAGAACTGCAA | 7468 |
rs754764236 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980845 | CTAACTTCTCCCAAA[A/G]TGTCCTAAGAAAATA | 7468 |
rs754764987 | snp | A/C | 1.90845e-05 | 0.003089 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974607 | ATGGAGGATGCTGGG[A/C]GCTCCAGCTCCCTGT | 7468 |
rs754765927 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952756 | TACTGCATCAGGTGT[C/T]GCCCGGCACAGTCTG | 7468 |
rs754805178 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | WHSC1 | GRCh38.p7 | 4:1916973 | CTTTTGAAGGAGAAG[A/G]ACAGTTTGAAAAATT | 7468 |
rs754815845 | snp | A/G | 1.67211e-05 | 0.00289142 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961159 | TAGACAAGGTAATGC[A/G]GAACTCCACTGTGAG | 7468 |
rs754816282 | snp | A/G | 1.64963e-05 | 0.00287192 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978717 | CCTCTGCCCCAATTC[A/G]TTCTGTAAGGAGCAC | 7468 |
rs754818685 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900095 | TTAGACTTTGCTGAC[C/T]AGGTCATCTTGGGCA | 7468 |
rs754851287 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964628 | AGACAAAGAGGTGCG[C/G]TGCGCTGCCGTTGTT | 7468 |
rs754858323 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891184 | CAGGTGTGAGCCACT[G/T]TGCCCCGCCTACGTG | 7468 |
rs754895784 | snp | A/G | 1.65111e-05 | 0.0028732 | missense | WHSC1 | GRCh38.p7 | 4:1900739 | GCACCAGAAATCCTC[A/G]GCAGTGCCAACGGGA | 7468 |
rs754927193 | in-del | -/C | 1.69579e-05 | 0.00291182 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952072 | GTGCAGAAGGGACTG[-/C]CGGGCGCTGCTTACC | 7468 |
rs754935293 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883292 | CTCAAGTAACAGTTT[C/T]TCAATGAACCCCACC | 7468 |
rs754947943 | snp | A/G/T | 5.39664e-05 | 0.0051943 | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1900641 | TGTTCTAAGAACGGA[A/G/T]GCATCTGGGCTGGAT | 7468 |
rs754994775 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948537 | TGTGGCTAGTTGTCT[G/T]TCCGGTGGCTGGGAG | 7468 |
rs754995102 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931099 | GGGAGGGAAGGTCGT[C/T]TCTTGGATTCCAGGC | 7468 |
rs754995253 | snp | A/G | 1.69801e-05 | 0.00291372 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952061 | TGTGGTAAGAGGTGC[A/G]GAAGGGACTGCCGGG | 7468 |
rs755011602 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897688 | CTGGAGTGCAGTGGC[A/G]TGGTCTTTGCTTATT | 7468 |
rs755030163 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886241 | AGACAGGATCTCACT[C/G]TGTGGCCAGGGCTGG | 7468 |
rs755039506 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962707 | TGAGACAGGGTCTCT[A/G]TCACCCAGGGTGGAG | 7468 |
rs755046921 | in-del | -/GTTAAGAGCAATGTGAGG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882006 | GTTCTTTTAGGTCCT[-/GTTAAGAGCAATGTGAGG]TTTTAAGGGTGATGG | 7468 |
rs755058552 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980753 | TGTGTAGCCACTGAC[C/T]TGCTCGCGCGGCCGT | 7468 |
rs755059449 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978346 | GCCCCTGCCTGTCCA[C/T]GCCGCGCTGGGGGAC | 7468 |
rs755083640 | snp | G/T | 1.65509e-05 | 0.00287666 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1930673 | GGAGATTGAAGAGCT[G/T]CTCAGGTCACAGTGG | 7468 |
rs755087337 | snp | C/T | 1.64966e-05 | 0.00287194 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959533 | AGAAATCCCTAAGTG[C/T]AACTGCAAGCCCACA | 7468 |
rs755091228 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880713 | CTACAGAGTTGCCAT[G/T]GGCAACACTGAGAAA | 7468 |
rs755121032 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951188 | AGTGACTGCCAAAAA[A/G]GAGTATGTGTGCCAG | 7468 |
rs755143294 | in-del | -/TCT | | | intron-variant, utr-variant-3-prime, cds-indel | WHSC1 | GRCh38.p7 | 4:1947141 | GTGCACAGCCTGCTG[-/TCT]GCAGTCGGCCAGACC | 7468 |
rs755144737 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875281 | AGTATAGCTTTTTAC[-/T]TTTTTTTTTTTTTTT | 7468 |
rs755146856 | snp | C/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870685 | CTCCCGCAGCCGCGC[C/T]CAGCTCCGGGTCGGA | 7468 |
rs755236557 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979491 | TTCTTTTCCATCCTA[A/G]TGAGAAGCTGGCCCT | 7468 |
rs755307566 | snp | C/G | 1.80107e-05 | 0.00300084 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953570 | GGTTCAGATGCAGGC[C/G]AGACGCAGGCCCATG | 7468 |
rs755316607 | snp | A/G | 1.83864e-05 | 0.00303197 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901270 | TTTAGGAGACGTTGT[A/G]TAAGGGGTCATGTGA | 7468 |
rs755319736 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873974 | GCTCAAGTGATTCTC[C/T]CGCCTCAGCCTCCTG | 7468 |
rs755321003 | snp | A/G | 1.73773e-05 | 0.0029476 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935102 | TCAAATGCAGCTTTT[A/G]GAGTGGTTTTCATGT | 7468 |
rs755333913 | snp | A/G | 3.29951e-05 | 0.00406159 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939676 | AAATCTGTCTGATGC[A/G]TGTAAACCACTGAAG | 7468 |
rs755354772 | snp | C/T | 1.66905e-05 | 0.00288876 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953490 | CTGTGTGAGCTGCCA[C/T]GCTTCCAACCCTTCA | 7468 |
rs755386252 | in-del | -/GTG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872525 | AGTATCAAAACTGAT[-/GTG]GTGACGTTAATCGTT | 7468 |
rs755390867 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959714 | GGCAAAGGGTGGGGC[C/T]TGGTCGCCAAGAGGG | 7468 |
rs755407561 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873029 | TTCCCCACAACTGAT[A/G]GTGGTTCAAATCTAA | 7468 |
rs755430719 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929848 | ACTGAGGCCAGACCC[A/G]GTGGGTTGGGTTGAT | 7468 |
rs755457925 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948559 | GGCTGGGAGGGGGTG[C/T]GGTGGGAAAAAGTCG | 7468 |
rs755474796 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886988 | CTTCTTCCCAACATT[C/G]CCAATATTGTGGTGG | 7468 |
rs755498921 | snp | G/T | 1.75566e-05 | 0.00296277 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974710 | AAACAGGACTGGTTT[G/T]GGGGTGTCCTGTCTC | 7468 |
rs755520256 | in-del | -/C | 0.000184089 | 0.00959222 | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1978832 | ACCAAGACTGAGAAG[-/C]CCCCCCCAGAGCCAG | 7468 |
rs755529148 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948433 | GGAGGTGGAGCCTGC[A/G]GCTGGAGTAAGGCTT | 7468 |
rs755529658 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933633 | TCTCCTGACCTCGTG[A/G]TCCACCCACCTCGGC | 7468 |
rs755540336 | snp | A/G | 1.65293e-05 | 0.00287479 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939820 | ATGGCATTGGTATGA[A/G]GGCCATTTAGCTGCC | 7468 |
rs755545318 | in-del | -/GAAG | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893120 | ACTCTAATCCCTTCC[-/GAAG]GTTCTTTGTCCTTGT | 7468 |
rs755548968 | snp | C/T | 1.6775e-05 | 0.00289607 | missense | WHSC1 | GRCh38.p7 | 4:1978809 | TAGGGGCGGCATCGG[C/T]CAGAAGCACCAAGAC | 7468 |
rs755558604 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966239 | GAAATGAAAGGATAC[C/T]ATACAGTCACTACAA | 7468 |
rs755586466 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916201 | ATTTGAACCCAGGTT[A/G]TGTGATGTCCGTATA | 7468 |
rs755599707 | in-del | -/TC | 1.88411e-05 | 0.00306923 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976715 | TGGCTTGCAGCTGTG[-/TC]TGTGTGGCAGGCTCC | 7468 |
rs755600481 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970161 | GGGCTGAGTCACATT[G/T]GGCGACGTCGTAAGT | 7468 |
rs755613185 | snp | G/T | 1.8263e-05 | 0.00302178 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953264 | TTAGTGGCTCAGAAC[G/T]GCAATTTAATTCTTG | 7468 |
rs755618120 | snp | A/T | 1.64833e-05 | 0.00287078 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953423 | AGGCTTGTGTGAAAA[A/T]ATACCCTCTGACTGT | 7468 |
rs755620801 | snp | C/T | 1.73809e-05 | 0.0029479 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978629 | CTCACATCTTGTGTT[C/T]TGTTGCAGGGAAGTG | 7468 |
rs755627841 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901450 | CCTCCTCAGTTCTCA[C/G]CTGGCTGCTGAGCCA | 7468 |
rs755636019 | snp | C/T | 1.80556e-05 | 0.00300457 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901245 | CTCAAGTCCTTCAGA[C/T]AAAAAGGTATTTAGG | 7468 |
rs755636910 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914645 | GTATGCTACTTTTCT[A/G]TCTTCACACTTGATT | 7468 |
rs755643031 | snp | C/G | 1.64999e-05 | 0.00287222 | missense | WHSC1 | GRCh38.p7 | 4:1978736 | TGTAAGGAGCACCAG[C/G]ACGGGACAGCCTTCA | 7468 |
rs755688117 | in-del | -/AT | 3.314e-05 | 0.00407049 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955894 | GTCTTTTCTGTTCAC[-/AT]GTGTTCGCTTTACAG | 7468 |
rs755697627 | snp | C/G | 7.60413e-05 | 0.00616562 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974617 | CTGGGAGCTCCAGCT[C/G]CCTGTCCTGTCCTCC | 7468 |
rs755757890 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921031 | CCACAGAGTGAGACC[-/CT]GTCTTAAACAAAAAA | 7468 |
rs755789196 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883725 | TGTAGTGGAAGCCCC[A/G]TGAAAGCAGGGCTCT | 7468 |
rs755796937 | snp | C/T | | | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978819 | ATCGGTCAGAAGCAC[C/T]AAGACTGAGAAGCCC | 7468 |
rs755819015 | snp | G/T | 3.29859e-05 | 0.00406102 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900753 | CGGCAGTGCCAACGG[G/T]AAGACTCCGAGCTGC | 7468 |
rs755824485 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977350 | GTGAGATGACTCTGG[C/T]GGTGCGCAGACATCA | 7468 |
rs755830786 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929023 | GGTGGAGTGCTGGGG[A/G]TCAGAGCCAGACCCA | 7468 |
rs755835567 | snp | A/G | 0.000197778 | 0.00994234 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951209 | TGTGTGCCAGGTGAG[A/G]AGAAGGCAGCATCCG | 7468 |
rs755837622 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877478 | TCTGCCATGTTTTTC[C/T]TCTGGGCCTTTGTGT | 7468 |
rs755856510 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938417 | TTTTTTTTTTCTTTC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTAAAT | 7468 |
rs755875832 | snp | A/G | 1.6552e-05 | 0.00287676 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955879 | ATCGTATGCTTTTAT[A/G]TCTTTTCTGTTCACA | 7468 |
rs755899508 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973453 | TGCACATCAGCACCG[C/T]GGCTCAGCGCGTCAT | 7468 |
rs755925398 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939340 | GTGCTAAACTTCTTA[C/T]GGATGAAATGATATG | 7468 |
rs755927733 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970889 | CCTCTGCCTCACAGT[A/G]AAAGGCTGAAAGCCC | 7468 |
rs755928823 | snp | C/G | 1.77153e-05 | 0.00297612 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974684 | CCTGACCTGTCCTCT[C/G]TGAGCAAGAGAAACA | 7468 |
rs755948082 | snp | C/T | 1.79319e-05 | 0.00299427 | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1900646 | TAAGAACGGAAGCAT[C/T]TGGGCTGGATGGAAT | 7468 |
rs755952585 | in-del | -/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979894 | TCTGCTTAGAGCACA[-/G]GAAGTGACAACTTAG | 7468 |
rs755959241 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922651 | CAGTATTTGGCCAGG[C/T]GTGGTGGCTTACGCC | 7468 |
rs755977468 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923496 | GAAGCTGTATGTTAC[A/G]ATCCTGGTGGGATGG | 7468 |
rs755979340 | snp | C/T | 1.65559e-05 | 0.00287709 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918257 | GTTCACCTTTCTCTA[C/T]GTGGGGGACCAGCTT | 7468 |
rs755996685 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903033 | TAAAATTAGCTGGGC[A/G]TGGTGGCACTGCCTG | 7468 |
rs755998702 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891311 | AGGGTATTTTAGGTA[C/T]GTGTAAATCATATTT | 7468 |
rs756068304 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913167 | GAAGTGACCAGAAGA[C/T]GAGTGTGAGCCCTCT | 7468 |
rs756089305 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880660 | AAGCTCCTATGTTTA[A/G]CAACCAATCTACAGG | 7468 |
rs756107227 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980889 | TAGATTTATGCTCCT[C/T]ATGATGCCCTAACTT | 7468 |
rs756112215 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970268 | AGGGGAGAAATAGGG[C/T]CAAGTGGAGGCTGTT | 7468 |
rs756117908 | snp | C/T | 4.94752e-05 | 0.00497344 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900858 | GAAGTTTAACGGCCA[C/T]GACGCCCTGCCCTTT | 7468 |
rs756118411 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887274 | GGAAGTGAGATCTGC[C/T]AGTCGTTTTAAATGC | 7468 |
rs756123835 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981610 | ACTCTTCAGGCACCT[G/T]AAGTGAGAACCCAGC | 7468 |
rs756132929 | in-del | -/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940350 | CATTGTAATATGACT[-/C]CTGTGTTCTGGACTT | 7468 |
rs756134493 | snp | C/T | 3.39098e-05 | 0.00411749 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952073 | TGCAGAAGGGACTGC[C/T]GGGCGCTGCTTACCC | 7468 |
rs756144891 | snp | G/T | 4.94531e-05 | 0.00497234 | missense | WHSC1 | GRCh38.p7 | 4:1959728 | CCTGGTCGCCAAGAG[G/T]GACATCAGAAAGGTA | 7468 |
rs756166955 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979616 | ACGTGTAGTTTACGC[A/G]GAGCACTTTCGAGGC | 7468 |
rs756213696 | snp | A/G | 1.64781e-05 | 0.00287033 | missense | WHSC1 | GRCh38.p7 | 4:1904262 | CTGGAAGAGACAAAG[A/G]CCACCTGTTGAAATA | 7468 |
rs756217385 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919425 | ATATAATTTTCTTAA[C/T]TGTTTGCATAAAATG | 7468 |
rs756222088 | in-del | -/CTC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923599 | TGAGCAACAGTGGGA[-/CTC]CTCATACAATGCTGG | 7468 |
rs756224321 | snp | A/G | 1.72481e-05 | 0.00293662 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935114 | TTTGGAGTGGTTTTC[A/G]TGTACATTTTCCCCA | 7468 |
rs756265543 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963525 | AAATGTAAACTACTT[A/G]TGTGCTGTAAGAAAT | 7468 |
rs756269168 | snp | C/T | 4.94556e-05 | 0.00497246 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959581 | CTTTGATTCGGAGTG[C/T]CTGAACAGGATGCTG | 7468 |
rs756306584 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979041 | CGTACAGGCCTCCTC[C/G]GGAGGGAGCGCCTCC | 7468 |
rs756311958 | snp | C/T | 2.11575e-05 | 0.00325243 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976477 | TTCTTGACTCTAGAC[C/T]TCGACGACCCTTTCA | 7468 |
rs756336608 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948581 | AAAAAGTCGGAATCT[C/G]TGCAATCTGTGTCAT | 7468 |
rs756394655 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886850 | CTCAAAAAAAAAATA[A/T]CTTGCTTATTTTGCT | 7468 |
rs756427704 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926199 | CTCGCACTGTTGCCA[G/T]GCTGGAGTGCAGAGG | 7468 |
rs756429370 | snp | C/T | 3.11871e-05 | 0.00394875 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978882 | GCGGCGGCGGAGGGG[C/T]TGGCGGAGAGTCACA | 7468 |
rs756444461 | snp | C/G | 1.68547e-05 | 0.00290294 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904412 | TGTTTTTCCAACTTT[C/G]TCTTCTGCACTTAAT | 7468 |
rs756450084 | snp | A/G | 1.64893e-05 | 0.0028713 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942438 | GCTGCTGCAGGTGGC[A/G]TATCATCGTACACAC | 7468 |
rs756451905 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895490 | TCTATTATATTTTTA[G/T]CTGTGCCTGGTCTGC | 7468 |
rs756500482 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894445 | GCTCAACCTGTAATC[C/T]TACCACTTTGGGAGT | 7468 |
rs756505343 | snp | C/T | 1.65614e-05 | 0.00287757 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939831 | ATGAAGGCCATTTAG[C/T]TGCCCACGCTGCAGT | 7468 |
rs756602723 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874854 | AAACTGTATGATTTG[C/T]TAATTCCTTTTTAAT | 7468 |
rs756624618 | snp | A/G/T | 5.03337e-05 | 0.00501645 | missense | WHSC1 | GRCh38.p7 | 4:1956138 | ACATGGAGGGGGACC[A/G/T]GGGCAGCCGCTACCA | 7468 |
rs756674028 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977664 | CCTGTAATCCCAGCT[-/A]ATTCGGGAGGCTGAG | 7468 |
rs756689265 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954422 | AGCTAGAATGCAGTG[A/G]TGTGATCATGGCTCA | 7468 |
rs756694783 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905980 | GCAGCCCGGGTGCAG[A/G]CACACATGGGTGTGT | 7468 |
rs756725942 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945709 | GTTTGATCCAGTTGA[C/G]TTGAAAGGGTTGCCT | 7468 |
rs756733500 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904164 | TTGGTCTTCTGGATA[C/T]ACAGGTAGTGATTGG | 7468 |
rs756739183 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939566 | AGATTCATCTTTAGA[A/G]CTTCACTTATTTGAG | 7468 |
rs756747615 | snp | A/G | 1.6563e-05 | 0.00287771 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939658 | TTATTTTACAGCAAC[A/G]AAAAATCTGTCTGAT | 7468 |
rs756755148 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957683 | AGGACAGGGAGCTCC[C/T]GACAGAACTCTGCCC | 7468 |
rs756767015 | snp | A/G | 3.30273e-05 | 0.00406356 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939798 | AATAATAATAATAAC[A/G]ATAACCATGGCATTG | 7468 |
rs756784125 | snp | A/C | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981704 | GCAGTGTTTGTCTGT[A/C]TTGACATCTAAACCC | 7468 |
rs756791339 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903452 | CCGAGACTTGCTCCT[A/G]GTCCTCCTGGTGCCC | 7468 |
rs756806595 | snp | C/T | 3.30753e-05 | 0.00406652 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918281 | CCAGCTTCATCTCAA[C/T]CCTCAAGTAGCCAAG | 7468 |
rs756820943 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869595 | GACCTCAGGCGATCC[A/G]CCTGTCTCGGCCTTC | 7468 |
rs756865033 | snp | C/G/T | 3.31654e-05 | 0.00407208 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955901 | CTGTTCACATGTGTT[C/G/T]GCTTTACAGTACTTA | 7468 |
rs756868763 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966517 | AAAAAATTAGCCGGG[C/T]GTGGTGGCAGGCGCC | 7468 |
rs756872091 | in-del | -/ACATAGAAAAATTAGCTGGTCGTGGTGGC | 1.65029e-05 | 0.00287248 | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1978739 | AGGAGCACCAGGACG[lengthTooLong]GGACAGCCTTCAGCT | 7468 |
rs756958859 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953207 | GAAACAGGGCCAGGT[C/G]CTTTAGCAGCATGGC | 7468 |
rs756987824 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968009 | TGGGAGAGAAATTGG[A/G]CCAGGTTCAAGTGGA | 7468 |
rs756992765 | snp | C/T | 6.13177e-05 | 0.0055367 | missense | WHSC1 | GRCh38.p7 | 4:1976482 | GACTCTAGACCTCGA[C/T]GACCCTTTCATCAGA | 7468 |
rs757012403 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962055 | TCATGGAAGACAGAT[A/G]TGATGAGACCTAGAG | 7468 |
rs757014062 | snp | C/T | 1.70391e-05 | 0.00291878 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935127 | TCATGTACATTTTCC[C/T]CATTCCCCATTCCAA | 7468 |
rs757015702 | snp | A/G | 3.30961e-05 | 0.0040678 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952201 | TCCCGGAGGCCAGAA[A/G]GGAGGTTCACCTGCA | 7468 |
rs757018945 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901334 | CACCTGCACGAGTAC[-/T]GGGGCGGGCGGAGAA | 7468 |
rs757021221 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916299 | TAAGAGGGAATAAAG[A/G]AGTGCATTTAGTCAG | 7468 |
rs757037495 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900759 | TGCCAACGGGAAGAC[C/T]CCGAGCTGCGAGGTG | 7468 |
rs757063957 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925307 | CTGTGCCTTCCTTTT[C/G]TAGGGTCCCTAGATG | 7468 |
rs757064937 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875815 | TCGGGAGGCTGAGGC[A/G]GGAGAATGGCGTTAA | 7468 |
rs757069326 | in-del | -/T | 1.83864e-05 | 0.00303197 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901270 | TTAGGAGACGTTGTG[-/T]TAAGGGGTCATGTGA | 7468 |
rs757084185 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911029 | TTTATCTCTGAGGCA[G/T]CCTTGTCTCTTGGTG | 7468 |
rs757103517 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892921 | AACCTCTGTATTTTT[A/G]TTTTTCACCTGAGTG | 7468 |
rs757135156 | snp | A/C | 1.64893e-05 | 0.0028713 | missense | WHSC1 | GRCh38.p7 | 4:1900863 | TTAACGGCCACGACG[A/C]CCTGCCCTTTATTCC | 7468 |
rs757146801 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879147 | GGCATGTGGTTCCTG[C/T]CTGTCTTTCCTTTAT | 7468 |
rs757155869 | snp | A/G | 2.46837e-05 | 0.00351301 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976612 | CGGGCAGCTGGTGCT[A/G]TGTGACCGCAAGTTC | 7468 |
rs757171367 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905655 | TGTTAGAGGGGCAGG[C/G]TGAGGACGAAGAGGA | 7468 |
rs757188334 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963574 | TTGCTTTTGATTAGT[-/A]AAAAAAGAAATGCCA | 7468 |
rs757196421 | snp | C/T | 6.61387e-05 | 0.00575021 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959749 | CAGAAAGGTATGTGT[C/T]GTTATCCCCTCCCCT | 7468 |
rs757206947 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947530 | GTCACTTTAATAAAA[A/G]TTGTTATGAACTATA | 7468 |
rs757224353 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872710 | AGCTCTTCAGTGCTA[C/T]CCACCTGCTTCACAG | 7468 |
rs757226225 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909085 | AAAAAAAAAGAGTTA[C/T]ATATTTTAGTTCTTA | 7468 |
rs757233317 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973639 | ATGTAGAAAGGACAC[A/G]GGGCCAGCGGTCCCA | 7468 |
rs757238305 | snp | A/G | 3.2962e-05 | 0.00405954 | missense | WHSC1 | GRCh38.p7 | 4:1916938 | AGAAAGAGCTTGGAT[A/G]TTTGAGAAGAGCCTC | 7468 |
rs757240426 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957852 | CATTGAAAGTTTAGA[A/G]TGAACTATAAAAATA | 7468 |
rs757242516 | snp | A/C | 1.64852e-05 | 0.00287094 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935179 | AGAAACCACACAAAG[A/C]GGATACAGGACCCTA | 7468 |
rs757283893 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972599 | GGCCGGGCAGCCCAC[A/G]TACCACGCACTGATG | 7468 |
rs757326330 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974331 | TTCTCCTGCCTCAGC[C/G]TCCCGAGTAGCTGAG | 7468 |
rs757373397 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898419 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCAAGG | 7468 |
rs757383616 | snp | C/G | 0.00013195 | 0.00812143 | missense | WHSC1 | GRCh38.p7 | 4:1955245 | GCTCAGTGATCGCCT[C/G]CAACAGCATCATCTG | 7468 |
rs757389883 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891020 | CACCTCAGCTTCCCG[C/T]GTAGCTAAGACCACA | 7468 |
rs757420003 | snp | A/G | 1.66302e-05 | 0.00288355 | missense | WHSC1 | GRCh38.p7 | 4:1978892 | AGGGGCTGGCGGAGA[A/G]TCACAGAGGGCAAAT | 7468 |
rs757426831 | snp | A/G | 0.000197925 | 0.00994602 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901047 | GAAAATCACCAAAAC[A/G]TACATGAATGGGAAG | 7468 |
rs757454935 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903695 | CCTGCTGTGTGCTAT[G/T]CACTGTCCTGATCCT | 7468 |
rs757456104 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935637 | GGCCGAGGCAGGTGG[A/T]TTGCTTGAGGTCAGG | 7468 |
rs757460901 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979859 | CGAAAGGAGTGACTT[C/T]GCAGGGCGTGAGACC | 7468 |
rs757473217 | snp | A/G | 0.000128364 | 0.00801033 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978840 | TGAGAAGCCCCCCCC[A/G]GAGCCAGGGAAGCCG | 7468 |
rs757480204 | snp | A/G | 8.24885e-05 | 0.00642164 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942446 | AGGTGGCGTATCATC[A/G]TACACACTCAGTGAC | 7468 |
rs757494380 | snp | A/G | 1.7494e-05 | 0.00295748 | missense | WHSC1 | GRCh38.p7 | 4:1955337 | TGCTTCGTGTGCTCC[A/G]AAGGTGAGGGGCCTG | 7468 |
rs757502678 | snp | A/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946849 | AGCCCGACAGGCCTC[A/T]TCTTTTTGGTTGGAT | 7468 |
rs757553364 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927614 | ATCCCAGCTACTCAG[G/T]AGGCTAAGGTGGGAG | 7468 |
rs757567692 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958377 | GAGTCAGTCACATAC[A/G]GCCAGGGCTCAGTGA | 7468 |
rs757584356 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896195 | ATGACTCCTCTCCTT[C/T]GGGCTCTGTGCAGGC | 7468 |
rs757593548 | snp | C/T | 1.69467e-05 | 0.00291085 | missense | WHSC1 | GRCh38.p7 | 4:1918558 | ACCACAGTCTCCATG[C/T]CACGAAGCAGGAAGG | 7468 |
rs757610283 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883873 | GCACGCAGGAGCTGC[A/G]TTGCTGCCTCTTGTT | 7468 |
rs757618633 | snp | C/T | 1.65455e-05 | 0.00287619 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975033 | GGACCCTGCATGGGG[C/T]TCCTGGCTATGGGGG | 7468 |
rs757619871 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884978 | AGCCAGGCGTGGTGG[C/T]GGCAACCTGTAATCT | 7468 |
rs757620436 | snp | A/C | 2.20709e-05 | 0.00332189 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918681 | TGAGGAACATCCCTT[A/C]AGTGCAGAATCATCT | 7468 |
rs757622754 | in-del | -/TGACTTCG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949966 | CCCAATTCCAATTTC[-/TGACTTCG]TGTTCATTGGCAAAC | 7468 |
rs757640726 | snp | A/G | 4.95062e-05 | 0.004975 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1957934 | CATTGACTTTTTAGC[A/G]CTGCAAGAAGCTGAA | 7468 |
rs757671449 | snp | A/G | 6.60317e-05 | 0.00574556 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951077 | TCATCTCTAGGTCTC[A/G]GACAGCCCGGGAGAC | 7468 |
rs757709000 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908709 | TCTGTGGAAAGGCAC[A/G]GGTCCCCATTGTCAC | 7468 |
rs757714898 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895701 | CTCAGTGGCTCTCCC[A/G]GGGAGAGGGGGGCTC | 7468 |
rs757725510 | snp | A/G | | | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1930730 | ACGCTACAACACCAA[A/G]TTTGCCCTGGTGGCC | 7468 |
rs757739573 | snp | C/T | 6.81896e-05 | 0.00583868 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956192 | TCTTCAAAAACGGTA[C/T]GGAGATATTCAGATA | 7468 |
rs757829574 | snp | A/C | 1.64914e-05 | 0.00287149 | missense | WHSC1 | GRCh38.p7 | 4:1901124 | CTCAGTCAGAAGAAA[A/C]TGGACAAAAACCAGA | 7468 |
rs757841844 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941327 | GTTGTTGCTTATACT[C/G]TTGTCAGGTACAGTA | 7468 |
rs757843495 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972270 | GACGGACACAAGAGA[C/T]GATATGGATGAGTGG | 7468 |
rs757846841 | snp | A/G | 0.000115556 | 0.00760032 | missense | WHSC1 | GRCh38.p7 | 4:1918396 | GTGAGAGAAGAGTGC[A/G]TTCCCATGAAGAGAA | 7468 |
rs757872063 | snp | A/C | 1.67792e-05 | 0.00289643 | missense | WHSC1 | GRCh38.p7 | 4:1918509 | AGAGGCTGACCCCAG[A/C]AGAGGAGTAGGGTCT | 7468 |
rs757879531 | in-del | -/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893543 | CTTTTTTTGTTTTTT[-/G]TTTTTTTTTTTTTTT | 7468 |
rs757894293 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893167 | TTTGTGAAAGAGATA[C/T]GCATATTAAACTCTC | 7468 |
rs757920884 | snp | A/C/G | 0.000386063 | 0.0138892 | missense | WHSC1 | GRCh38.p7 | 4:1956135 | CGTACATGGAGGGGG[A/C/G]CCGGGGCAGCCGCTA | 7468 |
rs757939635 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925487 | CACTGCAACCTCCTC[C/T]CCCCGGGTTCAAGCG | 7468 |
rs757961407 | snp | A/G | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1954665 | CAGCCTGTTTGCTCT[A/G]GTTTTAATGGCCCAT | 7468 |
rs757974328 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973722 | TCAGAGGCCGCGTGT[A/G]AATAGTGACTCCGAA | 7468 |
rs758001040 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873757 | AGCTGGAATTAGGCT[A/T]ACTAAGCTACAGGAT | 7468 |
rs758003833 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886142 | GTAATCAAAGGTGAC[A/G]GTCCCTGCTGTACTC | 7468 |
rs758003861 | in-del | -/AAG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965292 | GATAGAAAACCTATA[-/AAG]AGAAACAAACAAAAA | 7468 |
rs758030026 | snp | A/G | 1.67722e-05 | 0.00289583 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974791 | TCAATGTGCTTTATG[A/G]TGGTGAAAATTCCCT | 7468 |
rs758045507 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969993 | ACGGCACGAAGGTGG[A/G]TGTGGGGAGTGAGCA | 7468 |
rs758105062 | snp | C/G | 3.29647e-05 | 0.00405971 | missense | WHSC1 | GRCh38.p7 | 4:1900946 | GCACACGATGCCAAA[C/G]TGCGTTTTGAGTCCC | 7468 |
rs758107972 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917328 | ACACACACAGACAGA[C/G]GGATTAATGTAATGT | 7468 |
rs758138847 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905055 | GAATCGCTAGAACCC[A/G]GGAGGTGGAGGTTGC | 7468 |
rs758152260 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945500 | TCTAGTTCCAAAACC[-/A]AAAAAAAGTGCCTGT | 7468 |
rs758162681 | snp | A/G/T | 3.31566e-05 | 0.00407154 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935299 | TTGACCTGTCAGAGT[A/G/T]TATGCTCTGTGACTC | 7468 |
rs758163273 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883694 | CTTGTTTGTTGTCCC[C/T]ATCTGCTCTCCCAGC | 7468 |
rs758163785 | snp | C/T | 2.85702e-05 | 0.00377946 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976633 | CCGCAAGTTCTGCAC[C/T]AAGGCCTACCACCTG | 7468 |
rs758197617 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949703 | CAGGAGGCGGAGTTT[A/G]CAGTGAGCTGAGATT | 7468 |
rs758200373 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882192 | TTGTCCCTGCTTTGG[A/G]TCCCTGATTGGATTG | 7468 |
rs758205126 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913590 | TAGAAGAAATAATGT[A/G]AGCTGTCCCCTCTCT | 7468 |
rs758217696 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | WHSC1 | GRCh38.p7 | 4:1935195 | GGATACAGGACCCTA[C/T]AGAAGATGCTGAAGC | 7468 |
rs758225324 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899644 | GGCGGGTGCCTACCT[G/T]TTTCTTATTCCTAGC | 7468 |
rs758233415 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933842 | TTGCACTTACACCTT[A/C]CCGTCTTAGGTTGAT | 7468 |
rs758239297 | in-del | -/TTTC | 0.000239435 | 0.0109389 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938409 | TTCTTTTCTTTTTTT[-/TTTC]TTTCTTTTTTTTTTT | 7468 |
rs758288690 | snp | C/T | 3.30087e-05 | 0.00406242 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961121 | ACACGAGAACGACAT[C/T]ACCCACTTCTACATG | 7468 |
rs758313681 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941046 | GTGATGTTTGGACAC[A/G]CTGGAGAAAAGGCAG | 7468 |
rs758341344 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945705 | GCTCGTTTGATCCAG[C/T]TGAGTTGAAAGGGTT | 7468 |
rs758343111 | snp | A/G | 3.30497e-05 | 0.00406494 | missense | WHSC1 | GRCh38.p7 | 4:1955281 | CCCACTTCACTGCTC[A/G]GAAGGGGAAGCGACA | 7468 |
rs758376968 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962305 | CTAAAGAAGTACCCA[G/T]AGGAGGTGTGTGCTT | 7468 |
rs758400374 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916953 | ATTTGAGAAGAGCCT[C/T]GTAGCTTTTGAAGGA | 7468 |
rs758401011 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908864 | AGCTCACTCCAGGCT[C/G]AAACTCCTGGGCTCA | 7468 |
rs758408338 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960415 | GTCTAGGACCAAGTC[A/G]TTGGTAGACACCAGG | 7468 |
rs758429026 | snp | A/G | 1.80873e-05 | 0.00300721 | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1900634 | ACCATAGTGTTCTAA[A/G]AACGGAAGCATCTGG | 7468 |
rs758468007 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963739 | AAAAAACAAGCTGGG[C/G]ACAGTGGCCCACGCC | 7468 |
rs758482194 | snp | A/T | 1.89041e-05 | 0.00307436 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917077 | TTTTAGACCAGAAAT[A/T]TAATTTTTATTCTTT | 7468 |
rs758519104 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951086 | GGTCTCGGACAGCCC[A/G]GGAGACGAGCCCTCG | 7468 |
rs758529932 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926730 | CCCACCTCGGCCTCC[C/T]TAAGTGCTGGGATTA | 7468 |
rs758550808 | snp | A/G | 4.71731e-05 | 0.00485637 | missense | WHSC1 | GRCh38.p7 | 4:1978904 | AGAGTCACAGAGGGC[A/G]AATAGCGCCAGGCGG | 7468 |
rs758575975 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877168 | TTGTTATGCTTTTAG[A/G]GGATCTGTGCATGTT | 7468 |
rs758587367 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972778 | TTGCATAAGGCGGAG[G/T]CAGCTTTGTGAGAAA | 7468 |
rs758609124 | snp | A/G | 2.70742e-05 | 0.00367918 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918714 | TTCTCAGCATTATCA[A/G]GAGACTCTAACATGA | 7468 |
rs758671697 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966340 | GGTTTATAACTCCAT[C/T]TGTTTGTTTGTTGTC | 7468 |
rs758676908 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959116 | AGAGCTCTTACCAGC[A/G]TTTGCTGGACACCCT | 7468 |
rs758697327 | snp | C/G | 1.65018e-05 | 0.00287239 | missense | WHSC1 | GRCh38.p7 | 4:1901138 | AATGGACAAAAACCA[C/G]AAAACAAGGCGAGAA | 7468 |
rs758743496 | snp | C/T | 3.66824e-05 | 0.00428251 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901264 | AAGGTATTTAGGAGA[C/T]GTTGTGTAAGGGGTC | 7468 |
rs758747210 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951172 | AAAAGTCTGAGCGAG[G/T]AGTGACTGCCAAAAA | 7468 |
rs758747839 | in-del | -/AG | 1.71802e-05 | 0.00293084 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956207 | CGGAGATATTCAGAT[-/AG]AGAGTGAGACAGCAC | 7468 |
rs758754683 | snp | C/G | 1.65154e-05 | 0.00287358 | missense | WHSC1 | GRCh38.p7 | 4:1959508 | TCCAGATCTACACAG[C/G]GGATATTTCAGAAAT | 7468 |
rs758772953 | snp | C/G | 0.000198288 | 0.00995514 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953460 | GAGCCGAGGTTTCCG[C/G]TGCCCCCTCCACAGC | 7468 |
rs758784390 | snp | A/G/T | 5.08232e-05 | 0.00504078 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953279 | TGCAATTTAATTCTT[A/G/T]TTCTTTGCACCTCTC | 7468 |
rs758798576 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955871 | GACATAGAATCGTAT[A/G]CTTTTATGTCTTTTC | 7468 |
rs758798682 | snp | C/T | 1.65828e-05 | 0.00287943 | missense | WHSC1 | GRCh38.p7 | 4:1930663 | CTTCAGGTGAGGAGA[C/T]TGAAGAGCTGCTCAG | 7468 |
rs758808100 | snp | C/T | 3.33834e-05 | 0.00408541 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958082 | GGAGGGAGTCTTCCC[C/T]GAGGGCCGTGAGAGG | 7468 |
rs758809828 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | WHSC1 | GRCh38.p7 | 4:1975345 | TGGGCAATGAAAAAA[C/T]GGTCTGCCGGTGTGG | 7468 |
rs758818806 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916520 | CCGGCTAATTTTTGC[A/G]TTTTTCGTAGAGATG | 7468 |
rs758835228 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917549 | TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCCAAG | 7468 |
rs758848542 | in-del | -/ACACACACACACACACACACACACACACAA | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951496 | CACACACACACACAC[lengthTooLong]AGTTCCTGTTGGAAA | 7468 |
rs758861154 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885123 | TTCAAAAAAAAAAAA[A/T]AAAAATAAAAAAAAT | 7468 |
rs758923250 | snp | A/G | 4.95094e-05 | 0.00497517 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978744 | GCACCAGGACGGGAC[A/G]GCCTTCAGCTGCACC | 7468 |
rs758937965 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908375 | CAGCAGTCGGCTTCT[C/T]TAGGAATTATTGTGG | 7468 |
rs758956174 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945273 | TCTCATGTAGCTGGA[A/G]ACGTTAAGAGCTGAG | 7468 |
rs758985488 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978292 | AGTTGAAAATCAGTC[C/T]CTTGGGAGAGGGCAG | 7468 |
rs758998043 | snp | C/G | 5.2562e-05 | 0.00512623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930611 | TTCTCATTGCACCTT[C/G]TCCCGTTCCCACAGG | 7468 |
rs759061394 | snp | A/G | 4.9423e-05 | 0.00497082 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951115 | CGGAGTCCCCATACG[A/G]AAGTGCAGACGAAAC | 7468 |
rs759062431 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922141 | AATAGAATGAGTCTT[C/T]GTCTCCAAGAAAATA | 7468 |
rs759081224 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1954846 | GGGGATATTTTGGGG[A/G]TGTGCTCCTGGCATC | 7468 |
rs759107677 | snp | A/G | 3.29592e-05 | 0.00405938 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959614 | GTTTGAGTGCCACCC[A/G]CAGGTGTGTCCCGCG | 7468 |
rs759109142 | snp | C/G | 1.65288e-05 | 0.00287474 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975019 | GGTACAAGCTCTGGG[C/G]ACCCTGCATGGGGCT | 7468 |
rs759120776 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899631 | CCTTCCCAGCTGGGG[C/T]GGGTGCCTACCTGTT | 7468 |
rs759136436 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925687 | TACAGGCCTGAGCCA[C/G]TGCACCCAGCCTAGA | 7468 |
rs759138929 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876347 | TTCAACAAAATATAC[A/G]AGGATAGAAATTGCA | 7468 |
rs759177918 | snp | C/G | 0.000119573 | 0.00773126 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904179 | CACAGGTAGTGATTG[C/G]ATGTGTTAGTGTTTG | 7468 |
rs759179277 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896108 | CAGTGTAGTAAGTGG[C/T]AGAGCTGGGATTCTA | 7468 |
rs759281574 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953724 | TCCATCCTAAATATC[A/G]CCCTAAAGATGCTTA | 7468 |
rs759312671 | snp | C/G | 1.65468e-05 | 0.00287631 | missense | WHSC1 | GRCh38.p7 | 4:1978779 | ACGGGCGGTCCTACT[C/G]CTGTGAGCATGACTT | 7468 |
rs759314389 | snp | C/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870433 | AAGGCCGCCGGCTCC[C/G]GCAGCACCTGGAGGC | 7468 |
rs759323545 | snp | C/G | 1.72469e-05 | 0.00293652 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959459 | CCAAGACAGCTTACT[C/G]CTTCCCTGCAGGTGA | 7468 |
rs759328148 | snp | A/C/T | 5.06114e-05 | 0.00503027 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939631 | TATGATTTGAAACTT[A/C/T]ACAAACCAAAATTAT | 7468 |
rs759329018 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976888 | TCGAGCAGAGAAGAT[A/G]TGTGGTGACGGGGTA | 7468 |
rs759358068 | snp | C/T | 1.75167e-05 | 0.0029594 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953537 | AAGGTACAGGTGCAC[C/T]TGCGCAGCCTTGCTG | 7468 |
rs759377936 | snp | A/G | 1.65089e-05 | 0.00287301 | missense | WHSC1 | GRCh38.p7 | 4:1918357 | TCAGGAGTCAGTGAA[A/G]AAGCTGCTGAAAACC | 7468 |
rs759382288 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902556 | GTGCCCACAGCAGTA[G/T]TGAACCTCATGCTTT | 7468 |
rs759409501 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953400 | TCAGTGTGGAAAATT[C/T]TACCATGAGGCTTGT | 7468 |
rs759413044 | snp | A/G | 5.37524e-05 | 0.00518395 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974664 | CTCGGTCCTCTCCAC[A/G]TGGTCCTGACCTGTC | 7468 |
rs759432670 | snp | G/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1939755 | AAAAGTTCATCTCCT[G/T]CTGCATCCTTAACTG | 7468 |
rs759436893 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885763 | CCAGAGATCTCTGCA[C/T]CGGTTCTGCAGAGCT | 7468 |
rs759449575 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977122 | GGGCCCAGAGCCCCT[C/G]TCCTGGATGTGCAGG | 7468 |
rs759468329 | in-del | -/A | 1.65395e-05 | 0.00287567 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975026 | CTCTGGGGACCCTGC[-/A]ATGGGGCTCCTGGCT | 7468 |
rs759480103 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976098 | GCCCACCTGTGCCCA[C/T]GTTCCTGTGGAATTT | 7468 |
rs759482849 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884559 | CCACCACGCCTAGCT[A/G]ATTTTTATATTTTTA | 7468 |
rs759538323 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920569 | AAGTAAACACCCTGT[A/G]TTTATGGGGTATATG | 7468 |
rs759556940 | snp | A/T | 1.65633e-05 | 0.00287774 | missense | WHSC1 | GRCh38.p7 | 4:1918249 | AAAGCCAAGTTCACC[A/T]TTCTCTATGTGGGGG | 7468 |
rs759566032 | snp | C/T | 3.30929e-05 | 0.0040676 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955866 | TGTGAGACATAGAAT[C/T]GTATGCTTTTATGTC | 7468 |
rs759568073 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964241 | ATCAGACAAATACGA[A/G]CAAACAGCAGCGGAG | 7468 |
rs759597650 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923576 | AGAACAGCCAGGGAT[C/T]GAGAAGATGAGCAAC | 7468 |
rs759606146 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963299 | ACCCTCATGTGGGGA[C/T]CAGTGATAAGTCTTG | 7468 |
rs759613916 | in-del | -/GATT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886882 | ATTTTAGAACTTCCA[-/GATT]GATATATGTTCAATT | 7468 |
rs759644191 | snp | A/G | 3.45913e-05 | 0.00415866 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974735 | TGTCTCAGTGGACAC[A/G]GGACACCACGGTTTT | 7468 |
rs759652319 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882918 | GATGCCCTTGAGTTG[A/C]GAGCTACTGTCTGAA | 7468 |
rs759685528 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926740 | CCTCCCTAAGTGCTG[A/G]GATTATAGGTGTGAG | 7468 |
rs759703541 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913103 | TTCTACAATTATAAC[C/G]TAGGAAAAACCAGGT | 7468 |
rs759736468 | snp | C/T | 4.83734e-05 | 0.00491776 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976457 | TTCCGGTGATCTGTG[C/T]TTAATTCTTGACTCT | 7468 |
rs759790268 | snp | A/G | 1.67245e-05 | 0.00289171 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959791 | ATTACGGTTCACTGG[A/G]TAATTAGGCCTAGGT | 7468 |
rs759803629 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | WHSC1 | GRCh38.p7 | 4:1900908 | AAGATCTTACTTCCC[A/G]GGTGTTTAATGGAGA | 7468 |
rs759827746 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881683 | AATACAAGTATGAGC[C/T]ACCCCTCTGAGCCCT | 7468 |
rs759831523 | snp | A/G | 8.36169e-05 | 0.00646541 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952252 | TTCCCACGGGCGGGC[A/G]GCTCTGCAGCCTGGC | 7468 |
rs759841687 | snp | A/G | 2.02116e-05 | 0.0031789 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976576 | GCAGTCAGAGGACGA[A/G]TGCTTCCGCTGCGGT | 7468 |
rs759843722 | in-del | -/TTCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896806 | TTTCTTTCTCTCTCA[-/TTCT]TTCTTTCTTTCTTTT | 7468 |
rs759849071 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943267 | CCACAGTTAATTCCC[A/G]GCAGATTCTTTGGCT | 7468 |
rs759869545 | snp | C/G | 1.6549e-05 | 0.0028765 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952149 | GCTCTGTGAAGGACC[C/G]TGCTGCGGAGCTTTC | 7468 |
rs759880902 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935427 | TCTTACAGAACCCCA[C/T]TGAGAAAGGCTGCTT | 7468 |
rs759883854 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980330 | TGAGAAGGGGGCACC[A/G]TGTGTGCCTTTGCCC | 7468 |
rs759897619 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936392 | GATAATAGTTCTGGC[C/T]GGGTGTGGTAGCTCA | 7468 |
rs759922625 | snp | C/T | 9.89185e-05 | 0.00703203 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900768 | GAAGACTCCGAGCTG[C/T]GAGGTGAACCGCGAG | 7468 |
rs759932096 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874662 | AAGGTCACTCTGAAA[C/T]ATTGCAAGTATATAA | 7468 |
rs759937519 | snp | G/T | 1.67136e-05 | 0.00289076 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904395 | TATTGTGTTCTTTGG[G/T]TTGTTTTTCCAACTT | 7468 |
rs759943908 | in-del | -/C | 1.65255e-05 | 0.00287445 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935274 | GAAGGTAATTGTGTT[-/C]CAGGTTTGCTTGACC | 7468 |
rs759950918 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920914 | GTGATGGCATGTGCC[C/T]GTAGTCTCAACTACT | 7468 |
rs759969282 | in-del | -/TGTC | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981697 | CCCCTTCGCAGTGTT[-/TGTC]TGTCTTGACATCTAA | 7468 |
rs759984805 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928072 | TTTAAAAATAATTTC[-/T]TTTTTTTTTTTTTTC | 7468 |
rs759994519 | snp | A/G | 1.65334e-05 | 0.00287514 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1935163 | TGTAAATGGGAAAAA[A/G]AGAAACCACACAAAG | 7468 |
rs760004596 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972076 | CAAGAGGCAAACAGT[A/G]TCTCTCGGAGAATGT | 7468 |
rs760005243 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977025 | GGGAACTAAAGCCCC[-/T]CCTAGGAGAAAGGCC | 7468 |
rs760014428 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890670 | ACAATGGCATGATCT[C/T]GGCTCACTGCAACCT | 7468 |
rs760070505 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959653 | CTGCCAGAACCAGTG[C/T]TTCACCAAGCGCCAG | 7468 |
rs760077956 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969479 | CCGAGGCAGGAGAAC[C/T]GCTTGAGCCCAGCCT | 7468 |
rs760089102 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930512 | TTCCACGATGTGGGA[A/C]TAAAAATGCGACACA | 7468 |
rs760095870 | snp | A/G | 8.24831e-05 | 0.00642143 | missense | WHSC1 | GRCh38.p7 | 4:1955202 | CCCGTTGCCTATCAC[A/G]GCGGGGATGCTTGTC | 7468 |
rs760096114 | in-del | -/T | 5.537e-05 | 0.00526136 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900607 | TTTCTTTCTTTTTTC[-/T]TTTTTTTTAATACCA | 7468 |
rs760170097 | snp | C/T | 3.29745e-05 | 0.00406031 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916911 | TCACGTACAGTTCTT[C/T]GGTGACGCCCCAGAA | 7468 |
rs760185069 | snp | C/T | 6.67356e-05 | 0.0057761 | missense | WHSC1 | GRCh38.p7 | 4:1978800 | AGCATGACTTAGGGG[C/T]GGCATCGGTCAGAAG | 7468 |
rs760203894 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967694 | CTTTCTCGCTGCAGG[A/G]AAAGCCCATCTCTGA | 7468 |
rs760247979 | snp | A/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948004 | TTCACTAGGTTCCGT[A/T]ATGTTTGGTAATATC | 7468 |
rs760249298 | snp | A/T | 1.70799e-05 | 0.00292227 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930803 | CTGATGTCCTCTGCT[A/T]GGGTTGATGTGTGTA | 7468 |
rs760251680 | snp | A/C | 1.65375e-05 | 0.0028755 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959500 | CGGGAAAGTCCAGAT[A/C]TACACAGCGGATATT | 7468 |
rs760301543 | snp | C/G | 3.53513e-05 | 0.00420409 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953544 | AGGTGCACCTGCGCA[C/G]CCTTGCTGTGGGTTC | 7468 |
rs760320449 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1893988 | CAGGCTGCAGTACAG[C/T]GGCATGCTTATAGGT | 7468 |
rs760328069 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955555 | AATGACATTTGCTCT[C/T]GTGCTGATGTACAGA | 7468 |
rs760335527 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896176 | CGGCAGCCAGCTGCT[C/T]GCCATGACTCCTCTC | 7468 |
rs760365533 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897033 | TAGCTGGGCATGGTG[A/G]CAAGTGCCTTGTAGT | 7468 |
rs760413960 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882820 | GTTAGAAATGCACAT[A/T]TTCATGTCTCAGACC | 7468 |
rs760436780 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904061 | TTTTGATGAAACGAT[C/G]TTGAGGCTATCATCT | 7468 |
rs760444083 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946626 | AGGACTTTTTGTCAA[C/T]GAAATTGGTTTTGAT | 7468 |
rs760467400 | snp | C/T | 4.94328e-05 | 0.00497131 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974839 | TTGCTAACACTTGAC[C/T]GAATATATCACTTGA | 7468 |
rs760490927 | snp | A/G | 1.7122e-05 | 0.00292587 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974752 | GACACCACGGTTTTC[A/G]GTACAACAAGGAACA | 7468 |
rs760495179 | snp | A/C | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982347 | CCCGCTGGGGAGAGG[A/C]AGTGCCACCTTGGGA | 7468 |
rs760495462 | snp | C/T | 1.64838e-05 | 0.00287083 | intron-variant, utr-variant-3-prime, missense | WHSC1 | GRCh38.p7 | 4:1942357 | TTGTGGGAGCCCACA[C/T]CAGTCAAGTTGGATT | 7468 |
rs760499309 | snp | A/C/G | 4.95252e-05 | 0.004976 | missense | WHSC1 | GRCh38.p7 | 4:1918376 | CTGCTGAAAACCCCA[A/C/G]GTCTGTGAGAGAAGA | 7468 |
rs760525048 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905085 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCTA | 7468 |
rs760545655 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919797 | AAAAATTAGCTGGGC[A/G]TGGTGACGCGTGCTT | 7468 |
rs760548640 | snp | A/C/T | 3.30154e-05 | 0.00406286 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939794 | GTAAAATAATAATAA[A/C/T]AACGATAACCATGGC | 7468 |
rs760601317 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886537 | TTTATCTGTACTTTA[A/G]AAAGTAACTTGCGGC | 7468 |
rs760615361 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917136 | TACTTGCTCGAAATA[C/T]TGTAATGGCTTAACA | 7468 |
rs760640525 | snp | C/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870659 | CAGGCGTCCTCCCCT[C/T]GCGAGCGGTCCTCCC | 7468 |
rs760665991 | snp | C/T | 1.66457e-05 | 0.00288489 | missense | WHSC1 | GRCh38.p7 | 4:1956101 | GATTATTACTGGACG[C/T]ATCAGGCGCGAGTGT | 7468 |
rs760669938 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969360 | GACCCAGCCAGTACC[C/T]GCTCCAAGAAATCCG | 7468 |
rs760719802 | snp | A/G | 1.67792e-05 | 0.00289643 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952260 | GGCGGGCAGCTCTGC[A/G]GCCTGGCCGGCCACC | 7468 |
rs760749890 | snp | A/G | 1.65378e-05 | 0.00287552 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952171 | GGAGCTTTCCACCTC[A/G]CCTGCCTTGGGCTTT | 7468 |
rs760751111 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950776 | CTACTAGAGCAAATT[A/G]GATGTTCATAACACT | 7468 |
rs760779171 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965596 | AAGAGGAAAGCTACT[C/G]ATTACATGCAAGGTG | 7468 |
rs760781703 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914158 | CTCCCGAGTAGCTGG[C/G]ACTACAGGTGTGTGC | 7468 |
rs760807970 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899503 | GCTGTTCTAGTCCAC[A/G]GGCATCTCTGGTCCT | 7468 |
rs760850638 | in-del | -/GT | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947015 | CAAGAAATGACTGAG[-/GT]GTAGGGGTGGGGGTC | 7468 |
rs760883485 | in-del | -/CTTTTTTTTTTC | 2.05345e-05 | 0.00320419 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938401 | TCCTTTTTTTCTTTT[-/CTTTTTTTTTTC]TTTCTTTTTTTTTTT | 7468 |
rs760897959 | snp | C/T | 9.8956e-05 | 0.00703336 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900861 | GTTTAACGGCCACGA[C/T]GCCCTGCCCTTTATT | 7468 |
rs760909823 | snp | G/T | 1.67343e-05 | 0.00289255 | missense | WHSC1 | GRCh38.p7 | 4:1917034 | GAAAGCTGAGAAAAT[G/T]AAGGTGATAGATGAC | 7468 |
rs760935080 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944688 | ATATTGGCAATAGAG[G/T]TCCTGAATTGTTTTT | 7468 |
rs760950086 | in-del | -/TCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896770 | TTTCCTTCTTTCTTC[-/TCT]TTTTTTTCTTTTCTT | 7468 |
rs760954970 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976269 | AAGCTCACTCTAGTC[G/T]TAGTCTTTGTTCAGC | 7468 |
rs760958552 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968393 | GGGAGCACCGGGAGC[A/G]TGGTGACGCCAGGGT | 7468 |
rs760959004 | snp | C/T | 0.000140203 | 0.0083715 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938431 | CTTTTTTTTTTTTTT[C/T]TTTTTTTTTTAAATA | 7468 |
rs760971750 | in-del | -/AAC | 3.30115e-05 | 0.00406259 | cds-indel | WHSC1 | GRCh38.p7 | 4:1901141 | GGACAAAAACCAGAA[-/AAC]AAGGCGAGAAGGAAC | 7468 |
rs761020096 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964297 | CCTGGGATAATGGCA[G/T]AGCAGGAAGCTGTGT | 7468 |
rs761024107 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | WHSC1 | GRCh38.p7 | 4:1935246 | GACTCAGGACGGACA[A/G]GCACAGTCTTCGGAA | 7468 |
rs761025711 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922286 | TAAAATTAACATACA[A/G]GTGCAGCATCAAAGA | 7468 |
rs761030057 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973145 | CCACCGCGCCCGGCC[A/G]ACATATTGTTATAAA | 7468 |
rs761038727 | in-del | -/T | | | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974723 | TGGGGGTGTCCTGTC[-/T]TCAGTGGACACAGGA | 7468 |
rs761058778 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965318 | ACAAAAAAAGGAATT[G/T]TTGAGCCTGAGAAAC | 7468 |
rs761069462 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980533 | CATCTTTTATGCCTT[C/G]GTAAAAACTGCAGTG | 7468 |
rs761100221 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876765 | AATGCTTTTTTTTTC[C/T]GGAAGGAATTGGAAC | 7468 |
rs761102686 | snp | A/G | 1.68769e-05 | 0.00290485 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961182 | ACTGTGAGCTTCTGC[A/G]GTGTGCTGGACCTGG | 7468 |
rs761118436 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908523 | GAGTCAAGCCTGGGT[A/C]GATAACCCTCCAACT | 7468 |
rs761132766 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936549 | GGTGGTGCATGCCTG[C/T]AATCTCAGCTACTCG | 7468 |
rs761139847 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959959 | TCAGAATCCTGGGCT[C/G]AAGCCATCCTCCCAC | 7468 |
rs761159354 | snp | A/G | 1.65564e-05 | 0.00287714 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916878 | AAAACTAGGTCAGAA[A/G]AAGAGTGCACGCCAG | 7468 |
rs761183817 | snp | A/G | 5.74014e-05 | 0.005357 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978956 | CGGTGCAGGGCGGCC[A/G]GCCCTGCCTGCGGGA | 7468 |
rs761204359 | snp | A/G | 3.30246e-05 | 0.0040634 | missense | WHSC1 | GRCh38.p7 | 4:1955190 | TGTGTCCGCTGCCCC[A/G]TTGCCTATCACAGCG | 7468 |
rs761238128 | snp | A/G | 1.65523e-05 | 0.00287678 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951064 | TCATCCGCCTCCTTC[A/G]TCTCTAGGTCTCGGA | 7468 |
rs761298557 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873734 | TTCAGTGTAAAACAT[A/G]CAAAAGTAGCTGGAA | 7468 |
rs761302729 | snp | A/G | 1.69444e-05 | 0.00291066 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974770 | ACAACAAGGAACACA[A/G]CTTGTTCAATGTGCT | 7468 |
rs761312630 | snp | A/G | 2.60386e-05 | 0.00360813 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955665 | TAGCAGACAGGCTAA[A/G]CCTGGCCGCCTCGCC | 7468 |
rs761314503 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981154 | CTTCCAAATTTTATG[A/G]TTTTTCTGAAGGAAA | 7468 |
rs761315194 | snp | A/T | 1.83222e-05 | 0.00302668 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900616 | TTTTTTCTTTTTTTT[A/T]ATACCATAGTGTTCT | 7468 |
rs761342473 | snp | C/T | 1.66818e-05 | 0.00288802 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959780 | GCTTTTGAGAAATTA[C/T]GGTTCACTGGGTAAT | 7468 |
rs761346227 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920486 | CTATTATTGTGACTT[-/A]ACTGTGTAATGCTCA | 7468 |
rs761392809 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886554 | AAGTAACTTGCGGCT[C/G]GGCGCGGTGACTCAC | 7468 |
rs761407829 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917335 | CAGACAGAGGGATTA[A/G]TGTAATGTGATAGGA | 7468 |
rs761408365 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970640 | AGCCGCTGAGTCAGG[C/T]GGGAGCAGAAGCTGA | 7468 |
rs761418167 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918814 | ATACTCGACTTGCAC[C/T]CTGGGGTCTTAAAAT | 7468 |
rs761424608 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888014 | CACATCATCTTCTGC[A/G]ATGGACCATCTGTTT | 7468 |
rs761459706 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885846 | GGCGCAGGAATGATA[C/T]AGAAAAACTGAGTTG | 7468 |
rs761474418 | in-del | -/C | 0.000743108 | 0.0192614 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951253 | GGTGTCTGACTGGGG[-/C]CCCGGTACGCAGAGC | 7468 |
rs761486767 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906480 | CCTGGGCCCCAGTGA[C/T]CCGCTTGCCTCGGCC | 7468 |
rs761492339 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978174 | ACATTTTTGTACGGT[A/G]AAGATGACACACGAT | 7468 |
rs761501519 | snp | C/T | 2.44281e-05 | 0.00349477 | missense | WHSC1 | GRCh38.p7 | 4:1978868 | CCGAAGGGGAAGAGG[C/T]GGCGGCGGAGGGGCT | 7468 |
rs761521304 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926912 | TAACATGTTACCTCA[A/G]AACTTAGTGGCTGAA | 7468 |
rs761564037 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927798 | AATGTAATCTGAAGA[-/CT]CTAATTTGTAGAGTC | 7468 |
rs761579836 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943392 | ACTCCGTGGTTTCCT[A/G]TTGTGACAGTAATAA | 7468 |
rs761580469 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894860 | CTTAAGTGCATTCAC[A/G]TTGTTATACAACCAT | 7468 |
rs761598017 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944899 | TTTTATCTCTTATAC[C/G]TGTATCTCCCAACTA | 7468 |
rs761603597 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931449 | TTTGTGATAAATATG[G/T]GCTTGGATGTAAATT | 7468 |
rs761610395 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912199 | CCTCCCCAGAGGTAA[C/T]TATTTTTATCTCTTT | 7468 |
rs761633450 | snp | A/C/G | 5.30099e-05 | 0.00514807 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956228 | TGAGACAGCACTCTC[A/C/G]TGCATTTTCTTACCC | 7468 |
rs761645367 | snp | C/T | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1893878 | GATAATTTACCTGGG[C/T]ATAAAATTCTGGACA | 7468 |
rs761656654 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975616 | CTGGGGCTGCCAGAA[C/T]AATGCCTCACAGACG | 7468 |
rs761656656 | snp | C/T | 0.000155608 | 0.0088193 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918614 | CTTCTGTCAAAAACA[C/T]AGGGATGAGGTCAGT | 7468 |
rs761663126 | snp | A/G | 3.29723e-05 | 0.00406018 | missense | WHSC1 | GRCh38.p7 | 4:1900931 | AATGGAGAACCCGGC[A/G]CACACGATGCCAAAC | 7468 |
rs761680155 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952977 | TGATAAGTGACTGCT[C/T]CACCACTGGCCAGCT | 7468 |
rs761686189 | snp | C/T | 1.66557e-05 | 0.00288575 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951052 | ACTAGTGAACTGTCA[C/T]CCGCCTCCTTCATCT | 7468 |
rs761688358 | snp | A/T | 1.64762e-05 | 0.00287016 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974843 | TAACACTTGACCGAA[A/T]ATATCACTTGACCTT | 7468 |
rs761713452 | snp | A/G | 1.65222e-05 | 0.00287417 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958040 | AAGCACATCAAGGTG[A/G]CGTGTGGGAGCTGCG | 7468 |
rs761754548 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976256 | CAGGCTTCCGACAAA[C/G]CTCACTCTAGTCGTA | 7468 |
rs761768087 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905249 | AGGTTTTTCTGAAAG[G/T]TCTTCTAGAGTGAAG | 7468 |
rs761775786 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956982 | TAGGCATTGAAAGAT[G/T]TTAAAAAATTATTAA | 7468 |
rs761790715 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874451 | GGTAGGACTCTGTCA[C/T]TGCCTTGGGCAGCAT | 7468 |
rs761829106 | snp | A/T | 0.000143212 | 0.00846083 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938444 | TTTTTTTTTTTTTAA[A/T]TAATAGAGAGACACA | 7468 |
rs761830546 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950992 | GTGGTGGGGTGGGGC[A/G]GGACGAGCCTGCCTG | 7468 |
rs761844216 | snp | G/T | 1.76201e-05 | 0.00296812 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978608 | TGATTCCATCACTTC[G/T]GTGTGCTCACATCTT | 7468 |
rs761882008 | snp | C/T | 2.28925e-05 | 0.00338315 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953225 | TTAGCAGCATGGCTG[C/T]CTCTGAAGAGGAGTT | 7468 |
rs761882779 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895034 | TGGAATTTTACAGTA[-/T]TTTGTCTTTTTTGTG | 7468 |
rs761884031 | snp | C/T | 1.65288e-05 | 0.00287474 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935275 | AAGGTAATTGTGTTC[C/T]AGGTTTGCTTGACCT | 7468 |
rs761926241 | in-del | -/AGGCT | 1.66363e-05 | 0.00288407 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938576 | GGCTTCTGGGTGCCC[-/AGGCT]GGGCTGGGTGGGTGG | 7468 |
rs761932000 | snp | C/G | 1.66682e-05 | 0.00288684 | missense | WHSC1 | GRCh38.p7 | 4:1918195 | GAAATGGGCATTGTT[C/G]AAGCAGAAGAAGCTG | 7468 |
rs761935906 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937137 | ACTCACTGCAACCTC[C/T]GCCTCCTCGATTCAA | 7468 |
rs761943049 | snp | G/T | | | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939670 | AACGAAAAATCTGTC[G/T]GATGCATGTAAACCA | 7468 |
rs761945829 | snp | C/T | 1.65127e-05 | 0.00287334 | missense | WHSC1 | GRCh38.p7 | 4:1978692 | GCAAACCTTCGACTT[C/T]ATTTTGCCACCTCTG | 7468 |
rs761953956 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922360 | AAATGTCAGGTACTG[C/T]GGAATCAATATTACG | 7468 |
rs761973756 | snp | C/T | 0.00014247 | 0.00843889 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953553 | TGCGCAGCCTTGCTG[C/T]GGGTTCAGATGCAGG | 7468 |
rs761994266 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943608 | AGGGCTGGTTGGGTT[C/T]CTCTATTGGCTCTGC | 7468 |
rs762019994 | snp | C/G | 8.43576e-05 | 0.00649397 | missense | WHSC1 | GRCh38.p7 | 4:1900705 | TCAGAGTGTTGTAAA[C/G]TGCATAAAGATGAAG | 7468 |
rs762054309 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915963 | CATTTGACTTCAGTG[A/G]AATCTGGTACCTCCT | 7468 |
rs762060746 | snp | C/T | 0.000115307 | 0.00759211 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951149 | AACTGAAGTATCTGT[C/T]TCATCCAAAAAGTCT | 7468 |
rs762065468 | snp | C/T | 1.70119e-05 | 0.00291644 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961201 | TGCTGGACCTGGAGC[C/T]CTGATGGTCACCTGT | 7468 |
rs762128937 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938402 | CCTTTTTTTCTTTTC[-/TT]TTTTTTTTCTTTCTT | 7468 |
rs762131966 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909398 | TTGCAAGGGAAACTC[C/T]GTGCAGTAGGTCTCC | 7468 |
rs762163748 | snp | A/G | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952482 | GGCGGGCAGGGTGGC[A/G]GGATGACAGGTCATG | 7468 |
rs762168581 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961381 | GAGGCTCTGCTTGTC[C/T]GGGTGTGCATGCAGA | 7468 |
rs762204882 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924612 | AACTGAAGGTATACA[C/G]TTAAAACTGAGTTCT | 7468 |
rs762219852 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910468 | CTTTTAAGTTGGAAA[C/T]AGAAGATAACTATAT | 7468 |
rs762245596 | snp | C/T | 1.65441e-05 | 0.00287607 | missense | WHSC1 | GRCh38.p7 | 4:1955822 | TGCACTTCCAGGATA[C/T]CATTTGGGTGAAACT | 7468 |
rs762254504 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975310 | GACGGAGCTGACTTT[C/T]AACTACAACCTCGAT | 7468 |
rs762266599 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948096 | TTCTAAGGCAAATAG[A/G]CAACTTGGTACTATC | 7468 |
rs762277303 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982095 | TACTGAAATAGAGAG[C/T]TGAGACTTGCCAGTT | 7468 |
rs762278949 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898680 | AAAAAAACAAAAAAC[-/AAAA]AACACACTTTTTTTT | 7468 |
rs762285071 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973321 | ATGTAGGTTAGACAC[A/G]GTGCTGCCAGGCGTC | 7468 |
rs762293809 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960035 | CCTAATAATTTTATT[A/T]TTTTTTGGAGATGGG | 7468 |
rs762295992 | snp | G/T | 1.69873e-05 | 0.00291434 | missense | WHSC1 | GRCh38.p7 | 4:1930626 | CTCCCGTTCCCACAG[G/T]TGGTAGCTGAGCACC | 7468 |
rs762298789 | snp | C/T | 2.4238e-05 | 0.00348115 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955675 | GCTAAGCCTGGCCGC[C/T]TCGCCCTCCTCTTGC | 7468 |
rs762310321 | snp | A/T | 3.67181e-05 | 0.00428459 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900605 | CTTTTTCTTTCTTTT[A/T]TCTTTTTTTTAATAC | 7468 |
rs762314521 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957143 | GCAGACCACAGGACA[C/T]GTCTAGGGTTGACAT | 7468 |
rs762336879 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920821 | GGAGGATTGCTTGAG[A/C]CCATGAGTTTGAGAC | 7468 |
rs762349707 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878083 | CACACACTTCTGAGA[C/T]GGAGTCTAACTCTGT | 7468 |
rs762355523 | snp | A/G | 1.86235e-05 | 0.00305146 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978943 | CCGGATCCAGGGGCG[A/G]TGCAGGGCGGCCGGC | 7468 |
rs762403842 | snp | C/T | 1.66032e-05 | 0.0028812 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951057 | TGAACTGTCATCCGC[C/T]TCCTTCATCTCTAGG | 7468 |
rs762436092 | snp | C/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870057 | CTCAATTACTGTAGC[C/T]TTATAGTAAGTCTTG | 7468 |
rs762437664 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880376 | TGCCTCTTGGAAAAC[C/T]AACATACAGCAGTCT | 7468 |
rs762446198 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951244 | GTCCGTGCTGGTGTC[C/T]GACTGGGGCCCCGGT | 7468 |
rs762447502 | in-del | -/A | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869866 | TCTGTGTCTAGCCTG[-/A]TTTTTTTTTGCATGT | 7468 |
rs762458997 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942412 | CTTAGAATGATGTAA[C/T]ATTCCAGGATGCTGC | 7468 |
rs762462371 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907222 | CACCGGATGCTCGTA[G/T]TAGCAATTGTCATTA | 7468 |
rs762496382 | snp | G/T | 1.64969e-05 | 0.00287196 | missense | WHSC1 | GRCh38.p7 | 4:1901083 | CTTTGAATCTTCCAT[G/T]TGTGGTGACAGTGCT | 7468 |
rs762496768 | in-del | -/GTTA | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981852 | AGTTGATGACTGTTT[-/GTTA]GTCAGTAGAGTAAAA | 7468 |
rs762502247 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957842 | TATACTTAACATTGA[-/G]AAGTTTAGAGTGAAC | 7468 |
rs762528797 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888070 | TACCTTCATGTTTGG[C/T]GATACGTGGTCTGAT | 7468 |
rs762549754 | snp | A/T | 0.000156539 | 0.00884563 | missense | WHSC1 | GRCh38.p7 | 4:1918620 | TCAAAAACACAGGGA[A/T]GAGGTCAGTACTAAG | 7468 |
rs762556704 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958342 | CCTCCCACCTGCACC[A/G]GGCTGTTGCCAAGTG | 7468 |
rs762564946 | snp | A/G | 5.92663e-05 | 0.00544331 | missense | WHSC1 | GRCh38.p7 | 4:1978878 | AGAGGCGGCGGCGGA[A/G]GGGCTGGCGGAGAGT | 7468 |
rs762579850 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970973 | AGAGGAAAATGGGCT[C/T]GCTTACTTTTTAAAG | 7468 |
rs762637363 | snp | C/G/T | 0.000148599 | 0.0086186 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975013 | CCTGCAGGTACAAGC[C/G/T]CTGGGGACCCTGCAT | 7468 |
rs762652543 | snp | C/T | 3.56869e-05 | 0.004224 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930602 | GGATTTAACTTCTCA[C/T]TGCACCTTCTCCCGT | 7468 |
rs762693875 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884385 | TACAAGTGTGAGCCA[C/G]CGCAGGCCCCTTTTG | 7468 |
rs762708142 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961324 | GTCTTTCAGCTGCGC[C/T]GGAGGGCTAGAGCTA | 7468 |
rs762730973 | snp | C/T | 1.64977e-05 | 0.00287203 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978708 | ATTTTGCCACCTCTG[C/T]CCCAATTCGTTCTGT | 7468 |
rs762761295 | in-del | -/TG | 1.65053e-05 | 0.0028727 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951247 | GTGCTGGTGTCTGAC[-/TG]TGGGGCCCCGGTACG | 7468 |
rs762820570 | snp | C/T | 1.74604e-05 | 0.00295464 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959450 | ATGTGTGGACCAAGA[C/T]AGCTTACTCCTTCCC | 7468 |
rs762870190 | snp | C/G | 0.000115303 | 0.00759199 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953355 | CGTGTGTAAAGAGAG[C/G]AAGACAGATGTTAAG | 7468 |
rs762877969 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895112 | GAAGCAGATATCAGC[A/G]TTTCCTTCCTTTTAA | 7468 |
rs762916077 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890421 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAC | 7468 |
rs762958448 | snp | A/G | 5.02071e-05 | 0.00501009 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938581 | CTGGGTGCCCAGGCT[A/G]GGCTGGGTGGGTGGG | 7468 |
rs762964466 | snp | A/G | 5.7363e-05 | 0.0053552 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974595 | TTGTTTGCCATCATG[A/G]AGGATGCTGGGAGCT | 7468 |
rs762967872 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883229 | CCATTTCAGGTTCAG[A/G]AACAAGAGAAAGCCC | 7468 |
rs762977766 | snp | A/G | 4.98409e-05 | 0.00499179 | missense | WHSC1 | GRCh38.p7 | 4:1918216 | GAAGAAGCTGCAAGC[A/G]TGTCAGTGGAGGAGC | 7468 |
rs763004569 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976340 | AGCACGAGGAGGACA[C/G]TCCTCTCCTCTCCTC | 7468 |
rs763005063 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895922 | TGGTAGAGGGGCTCA[G/T]GTGATGATGACAGCA | 7468 |
rs763015872 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892058 | AATATTAGCACCTCA[A/G]GAATAAGGAAGGCAT | 7468 |
rs763018932 | snp | C/G | 1.65419e-05 | 0.00287588 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938488 | CGGCCAGAACAAGCT[C/G]TTACAAGGCCATGGA | 7468 |
rs763045047 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961746 | CCTGACAGGTGTTGC[C/T]GGGCCCTTCCAGGGC | 7468 |
rs763053114 | snp | C/T | 1.65364e-05 | 0.0028754 | missense | WHSC1 | GRCh38.p7 | 4:1978772 | ACCCCGGACGGGCGG[C/T]CCTACTGCTGTGAGC | 7468 |
rs763068371 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892619 | CGCCCAGGCTGGAGT[A/G]TAGTGGCCTGATCTC | 7468 |
rs763089072 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970068 | AGGAAAGAAAGAGAA[A/G]GATGCGAGTGACGCC | 7468 |
rs763092641 | in-del | -/A | 1.67379e-05 | 0.00289287 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974796 | TGCTTTATGATGGTG[-/A]AAAATTCCCTTTAAA | 7468 |
rs763121574 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940222 | TGTTGCTTCCAGACC[G/T]AGGCTCATGGAGGAA | 7468 |
rs763123333 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903993 | CCCACGTTGGCCTCC[C/T]AAAGTGCTGGGACTA | 7468 |
rs763138074 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924947 | AAACTACAAAAAATT[A/G]AGCTCTGTGTTAATG | 7468 |
rs763140205 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973340 | CTGCCAGGCGTCAGA[A/G]GCTGGGTTGTCCTGT | 7468 |
rs763156265 | snp | C/T | 1.64871e-05 | 0.00287111 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900837 | CCTGCAGGAGGGGGT[C/T]ATGCAGAAGTTTAAC | 7468 |
rs763158326 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915380 | CGGCCTCCCAAAGTG[A/C]TGGGATTACAGGCTT | 7468 |
rs763160021 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879689 | GTCCCATGGATCTTT[C/G]CATGTGCTGTTGCTT | 7468 |
rs763173652 | snp | C/T | 1.71979e-05 | 0.00293235 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930817 | TTGGGTTGATGTGTG[C/T]AGTGTAGCAAGCTGA | 7468 |
rs763209260 | snp | A/G | 4.95413e-05 | 0.00497677 | missense | WHSC1 | GRCh38.p7 | 4:1918336 | TTGGGAGAAATGGCA[A/G]AATCCTCAGGAGTCA | 7468 |
rs763211280 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882194 | GTCCCTGCTTTGGGT[C/G]CCTGATTGGATTGGA | 7468 |
rs763234052 | snp | A/G | 1.66399e-05 | 0.00288438 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955972 | AATCCTGTTTTTAAT[A/G]TTTATAATAGATGGT | 7468 |
rs763292766 | snp | A/C/G | 3.30574e-05 | 0.00406544 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955841 | TTGGGTGAAACTTGG[A/C/G]AACTACAGGTGTGAG | 7468 |
rs763297964 | snp | C/T | 5.30518e-05 | 0.00515006 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976445 | CTGTGTAATTCTTTC[C/T]GGTGATCTGTGCTTA | 7468 |
rs763313051 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881602 | GGGTTTTGCCATGTT[G/T]CCCAGGCTGGTCTTG | 7468 |
rs763327138 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910567 | GGAGATTTTTGTTGT[C/T]ACCTTTTCTGTGTTA | 7468 |
rs763353266 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912509 | TTGAAATCATACACT[A/G]TGTTGTCCATACAGC | 7468 |
rs763368806 | snp | A/C/G | 1.67553e-05 | 0.00289437 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978807 | CTTAGGGGCGGCATC[A/C/G]GTCAGAAGCACCAAG | 7468 |
rs763371145 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886753 | TGAGGCAGGGTACTC[A/G]CTTGAACCTGGGGAG | 7468 |
rs763383769 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933344 | CCAACAGTAGTGAGG[C/G]TTGAGGGTGACAGCG | 7468 |
rs763391826 | snp | C/G | 1.64746e-05 | 0.00287002 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959701 | CATCAAGACAGATGG[C/G]AAAGGGTGGGGCCTG | 7468 |
rs763391838 | snp | A/G | 3.8398e-05 | 0.0043815 | missense | WHSC1 | GRCh38.p7 | 4:1976563 | GGGAAGGGAAGAGGC[A/G]GTCAGAGGACGAGTG | 7468 |
rs763411971 | snp | C/T | 6.80816e-05 | 0.00583405 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952058 | CCTTGTGGTAAGAGG[C/T]GCAGAAGGGACTGCC | 7468 |
rs763413199 | snp | A/G | 9.93229e-05 | 0.00704639 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904230 | GATTCCAGCTAAGAA[A/G]GAGTCTTGTCCAAAC | 7468 |
rs763432475 | in-del | -/AC | 0.00105819 | 0.0229777 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918116 | TGTGTAGTGAAACTT[-/AC]AGTGTCTCTTTTTTT | 7468 |
rs763435186 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899351 | CGCGGGCATCCTGTG[C/T]GTTGCAGGAGATGCA | 7468 |
rs763455779 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924589 | ATACTAAAAGTAATA[A/T]AAAACCAAACTGAAG | 7468 |
rs763491250 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962985 | CCTGTCAACACAGGT[A/C]TTCTCTAGGAGGTGG | 7468 |
rs763540025 | in-del | -/GTC | 3.54359e-05 | 0.00420912 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978589 | CACGATAATGTTGAA[-/GTC]GTGATTCCATCACTT | 7468 |
rs763550891 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939103 | AACTCTTAATTAAAA[G/T]GAAAACAAAACCCTG | 7468 |
rs763556288 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977658 | GCATGCACCTGTAAT[C/G]CCAGCTATTCGGGAG | 7468 |
rs763576743 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953440 | TACCCTCTGACTGTA[C/T]TTGAGAGCCGAGGTT | 7468 |
rs763599385 | snp | G/T | 1.66076e-05 | 0.00288158 | missense | WHSC1 | GRCh38.p7 | 4:1935150 | CATTCCAAGGTAATG[G/T]AAATGGGAAAAAAAG | 7468 |
rs763621147 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916208 | CCCAGGTTGTGTGAT[A/G]TCCGTATACTGCCTC | 7468 |
rs763645701 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885789 | GAGCTGCCCTGAGTA[C/T]AGGTAGTTCCTCACT | 7468 |
rs763675137 | in-del | -/AAAAG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908561 | GATTCAGATAATCTT[-/AAAAG]AAAAGGGGTCAAAGG | 7468 |
rs763694234 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884734 | CTATTTGTAGAAGAC[A/G]AATTGGGATTATATA | 7468 |
rs763723156 | snp | A/G | 1.64743e-05 | 0.00287 | missense | WHSC1 | GRCh38.p7 | 4:1959667 | GCTTCACCAAGCGCC[A/G]GTACCCAGAGACCAA | 7468 |
rs763728499 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872117 | TGTCTGGCGTTGACA[C/T]TCGCGGCGCCCGGGC | 7468 |
rs763756758 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890536 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCACCT | 7468 |
rs763763062 | in-del | -/AAA | | | utr-variant-3-prime, cds-indel | WHSC1 | GRCh38.p7 | 4:1982045 | TTGATAGTTAGACTT[-/AAA]AACTTGAAATTCACT | 7468 |
rs763784548 | snp | C/G | 1.76577e-05 | 0.00297129 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974692 | GTCCTCTGTGAGCAA[C/G]AGAAACAGGACTGGT | 7468 |
rs763811771 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947402 | AAGACGACTGTGGTG[G/T]GCAGTGGTGCTCTGG | 7468 |
rs763826246 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978083 | AGTGAGCCAAGATTG[C/T]GCCACTGCTCTCCAG | 7468 |
rs763826395 | snp | A/G/T | 5.00549e-05 | 0.00500254 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978801 | GCATGACTTAGGGGC[A/G/T]GCATCGGTCAGAAGC | 7468 |
rs763848266 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880395 | ATACAGCAGTCTATA[-/TG]TGCATGGAAGACTGA | 7468 |
rs763851539 | snp | C/G/T | 8.28664e-05 | 0.00643639 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939657 | ATTATTTTACAGCAA[C/G/T]GAAAAATCTGTCTGA | 7468 |
rs763866207 | snp | A/G | 1.70362e-05 | 0.00291853 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974761 | GTTTTCAGTACAACA[A/G]GGAACACAACTTGTT | 7468 |
rs763870560 | in-del | -/TGTC | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939481 | GTTCATTGTACAGTT[-/TGTC]TGCTTTTGTTTATGT | 7468 |
rs763898184 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940598 | TGTTATTTGGTTCTC[C/T]GTGATGCTGTTTTTC | 7468 |
rs763967226 | snp | C/G | 1.72543e-05 | 0.00293715 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956214 | ATTCAGATAGAGAGT[C/G]AGACAGCACTCTCGT | 7468 |
rs763969166 | snp | C/T | 3.3083e-05 | 0.00406699 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952189 | TGCCTTGGGCTTTCC[C/T]GGAGGCCAGAAGGGA | 7468 |
rs763971458 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904165 | TGGTCTTCTGGATAC[A/G]CAGGTAGTGATTGGA | 7468 |
rs764003787 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969779 | AAGCCACTTAGAAAA[A/G]TTTTTATCACAAAGT | 7468 |
rs764009190 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904083 | CTATCATCTAAAACA[C/T]AGCAAGGGAGCACAC | 7468 |
rs764038848 | snp | A/G | 1.64879e-05 | 0.00287118 | missense | WHSC1 | GRCh38.p7 | 4:1900928 | TTTAATGGAGAACCC[A/G]GCGCACACGATGCCA | 7468 |
rs764069916 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1903103 | AAAAACATGAAAATG[G/T]GTCATGTGGCAGCTC | 7468 |
rs764115651 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978428 | TAACAGGTGGTCCTT[A/G]GGGGCCTGGCAGGTA | 7468 |
rs764157294 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916929 | TGACGCCCCAGAAAG[A/G]GCTTGGATATTTGAG | 7468 |
rs764157520 | in-del | -/TTTTTTGTTTTTTTTTT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893537 | TTGCCTCTTTTTTTG[-/TTTTTTGTTTTTTTTTT]TTTTTTGTTTTGTTT | 7468 |
rs764181204 | snp | C/T | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952454 | GTGCCCCCTTGGTAC[C/T]TTTCCATCAGGTGGC | 7468 |
rs764192423 | in-del | -/CTGA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877406 | TCTCTCACTGGCTTT[-/CTGA]CTCTCACTGCACTAC | 7468 |
rs764196569 | snp | C/G | 0.000302277 | 0.0122901 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952263 | GGGCAGCTCTGCAGC[C/G]TGGCCGGCCACCTGC | 7468 |
rs764213274 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889061 | CGCTACCATGCCTGG[C/G]TAATTTTTGTATTTT | 7468 |
rs764222600 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950836 | ATGCATATATATGCT[A/T]AATACTAGGTAGAAT | 7468 |
rs764264215 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973400 | CCCCGTGCTGTCCTC[A/G]TCCCCAGGGCCCTGC | 7468 |
rs764285924 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914168 | GCTGGGACTACAGGT[A/G]TGTGCCACCGTGCCC | 7468 |
rs764290922 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938401 | CCTTTTTTTCTTTTC[-/T]TTTTTTTTTTCTTTC | 7468 |
rs764317810 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939374 | GGATTTGCTTCAGAA[-/T]TAATCTGGCAGGGGG | 7468 |
rs764327216 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979805 | CAAATCACCACCGAC[C/T]GAAGTGTGTGTTTAC | 7468 |
rs764338341 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955562 | TTGCTCTCGTGCTGA[-/TG]TGTACAGATCGCTGT | 7468 |
rs764357158 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913507 | CCTGTACATCTGGCT[C/G]CGCCTTCTAGATAGC | 7468 |
rs764366426 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961106 | GAGAATCAAGCACGC[A/G]CACGAGAACGACATC | 7468 |
rs764374372 | snp | C/T | 6.82105e-05 | 0.00583957 | missense | WHSC1 | GRCh38.p7 | 4:1978886 | CGGCGGAGGGGCTGG[C/T]GGAGAGTCACAGAGG | 7468 |
rs764390103 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896177 | GGCAGCCAGCTGCTC[G/T]CCATGACTCCTCTCC | 7468 |
rs764412371 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960006 | GCTGGGACTACAGGC[A/G]TGTTTGACCATGCCC | 7468 |
rs764419757 | snp | C/G | 1.76827e-05 | 0.00297339 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978599 | TTGAAGTCGTGATTC[C/G]ATCACTTCTGTGTGC | 7468 |
rs764446522 | in-del | -/TTT | 1.82061e-05 | 0.00301708 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901254 | TCAGATAAAAAGGTA[-/TTT]TTTAGGAGACGTTGT | 7468 |
rs764467816 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951122 | CCCATACGAAAGTGC[A/G]GACGAAACACAAACT | 7468 |
rs764468148 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909277 | ACCCCCCCCAACCCT[A/G]GCATCAGCCGTTTCT | 7468 |
rs764479216 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899541 | CTCAGATTTTCCCTA[C/G]TGTCTGATGCTATTG | 7468 |
rs764480753 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887034 | AGAACTTAGTGGTTG[-/A]AAAAAACAACAACCT | 7468 |
rs764490108 | snp | C/G | 0.000115724 | 0.00760584 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975021 | TACAAGCTCTGGGGA[C/G]CCTGCATGGGGCTCC | 7468 |
rs764506321 | snp | C/T | 6.60687e-05 | 0.00574717 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951075 | CTTCATCTCTAGGTC[C/T]CGGACAGCCCGGGAG | 7468 |
rs764519174 | snp | A/G | 1.96914e-05 | 0.00313773 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918661 | TGCTAGCAAGTTTCA[A/G]AATTTGAGGAACATC | 7468 |
rs764520817 | snp | C/T | 4.98567e-05 | 0.00499258 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955672 | CAGGCTAAGCCTGGC[C/T]GCCTCGCCCTCCTCT | 7468 |
rs764522182 | snp | A/T | 1.82958e-05 | 0.00302449 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900617 | TTTTTCTTTTTTTTA[A/T]TACCATAGTGTTCTA | 7468 |
rs764542983 | snp | G/T | 1.69438e-05 | 0.00291061 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917046 | AATTAAGGTGATAGA[G/T]GACCCTTCAGTCTAC | 7468 |
rs764556198 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921129 | GATATGTATCAGAAG[C/G]TTTCATCAAGGATAT | 7468 |
rs764569364 | snp | A/G | 3.3151e-05 | 0.00407117 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958063 | GAGCTGCGTGCACGC[A/G]TGTGGAGGGAGTCTT | 7468 |
rs764587783 | in-del | -/A | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869878 | CTGATTTTTTTTTGC[-/A]TGTGGACATCCAGTT | 7468 |
rs764588265 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957478 | TTTTTGTAGAGAATG[A/G]GGTTTCAGCATGTTG | 7468 |
rs764599848 | snp | A/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945547 | AAGATGATAAGAAAG[A/T]GCTCCTGAGAAGGCT | 7468 |
rs764628718 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936760 | TCACTGATCTGAGTT[A/G]AAATGCTCTTTTTAT | 7468 |
rs764690024 | snp | C/T | 1.65149e-05 | 0.00287353 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939800 | TAATAATAATAACGA[C/T]AACCATGGCATTGGT | 7468 |
rs764690901 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958855 | TCATACCACAGCAGT[G/T]AAAAGAGTGTCTTTC | 7468 |
rs764719975 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876785 | GGAATTGGAACCTCA[A/G]TTTTTAAGTTGACTT | 7468 |
rs764735851 | snp | A/C | | | missense | WHSC1 | GRCh38.p7 | 4:1904279 | CACCTGTTGAAATAC[A/C]ACGTTGGTGATTTGG | 7468 |
rs764764393 | snp | C/T | 1.65026e-05 | 0.00287246 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955195 | CCGCTGCCCCGTTGC[C/T]TATCACAGCGGGGAT | 7468 |
rs764769330 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918822 | CTTGCACTCTGGGGT[C/T]TTAAAATATCCTTCC | 7468 |
rs764857873 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872532 | AAACTGATGTGGTGA[C/G]GTTAATCGTTTTTAG | 7468 |
rs764880891 | snp | G/T | 1.67472e-05 | 0.00289367 | missense | WHSC1 | GRCh38.p7 | 4:1918497 | TCAAAAGACGGCAGA[G/T]GCTGACCCCAGAAGA | 7468 |
rs764882068 | in-del | -/TTTTTTTTTTCTTTCTTTTTTTTTT | 0.000166764 | 0.00912985 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938402 | CCTTTTTTTCTTTTC[-/TTTTTTTTTTCTTTCTTTTTTTTTT]TTTTTTTTTTTTTTT | 7468 |
rs764915930 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886706 | AGCCAGGCGTGGTGG[C/T]GTGCACCTGTAGTCC | 7468 |
rs764917391 | snp | G/T | 1.66946e-05 | 0.00288912 | missense | WHSC1 | GRCh38.p7 | 4:1956126 | GAGTGTTCCCGTACA[G/T]GGAGGGGGACCGGGG | 7468 |
rs764947357 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931477 | ATTGTGGAAAACTGA[G/T]ATTTGAATGTAAAAA | 7468 |
rs764948196 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888114 | TATGTGTGAGGCAAC[A/G]TTTATTAAGGCTATA | 7468 |
rs764959960 | snp | A/G | 1.73408e-05 | 0.0029445 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918617 | CTGTCAAAAACACAG[A/G]GATGAGGTCAGTACT | 7468 |
rs764970673 | snp | G/T | 5.07722e-05 | 0.0050382 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974773 | ACAAGGAACACAACT[G/T]GTTCAATGTGCTTTA | 7468 |
rs764972283 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969975 | AGAGTAGGAACCACA[A/G]GAACGGCACGAAGGT | 7468 |
rs764993331 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944793 | GATGGATCTTTGGGC[C/T]TTTCCTCAGTGTTCA | 7468 |
rs765002658 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882162 | GGTCACTCTGTTCAG[G/T]TGAAAACCTTTCCTT | 7468 |
rs765043376 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933250 | ATTGGCAGCAGGGCA[C/T]GGACACTTACTTGTA | 7468 |
rs765067172 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894867 | GCATTCACATTGTTA[C/T]ACAACCATGACACTG | 7468 |
rs765090322 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | WHSC1 | GRCh38.p7 | 4:1901057 | AAAACATACATGAAT[A/G]GGAAGCCTCTCTTTG | 7468 |
rs765097136 | snp | A/G | 5.05276e-05 | 0.00502606 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952269 | CTCTGCAGCCTGGCC[A/G]GCCACCTGCTCCTGC | 7468 |
rs765103395 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925309 | GTGCCTTCCTTTTCT[A/G]GGGTCCCTAGATGTA | 7468 |
rs765117080 | snp | C/T | 1.65485e-05 | 0.00287645 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935283 | TGTGTTCCAGGTTTG[C/T]TTGACCTGTCAGAGT | 7468 |
rs765152046 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957052 | CTGCGACTGTCGGCA[A/G]AGTCTCCTAACTGTG | 7468 |
rs765152112 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940905 | CTCTGAATCCTCAGC[A/G]ACCACTCCTCCGAGT | 7468 |
rs765159838 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963526 | AATGTAAACTACTTA[G/T]GTGCTGTAAGAAATG | 7468 |
rs765170518 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973692 | GCACCAGGGCTGGGT[A/G]CGTGGGCAGTTGTGT | 7468 |
rs765179536 | snp | A/C | 2.28011e-05 | 0.00337639 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953226 | TAGCAGCATGGCTGC[A/C]TCTGAAGAGGAGTTG | 7468 |
rs765231387 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885764 | CAGAGATCTCTGCAC[C/T]GGTTCTGCAGAGCTG | 7468 |
rs765286171 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975630 | ACAATGCCTCACAGA[C/T]GCGTGGTTTCGCAGT | 7468 |
rs765310450 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879323 | TCCTGGGTTCACACC[A/G]TTCTCCTGCCTCAGC | 7468 |
rs765322032 | snp | A/G | 5.46582e-05 | 0.00522744 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900622 | CTTTTTTTTAATACC[A/G]TAGTGTTCTAAGAAC | 7468 |
rs765338279 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973333 | CACGGTGCTGCCAGG[C/T]GTCAGAGGCTGGGTT | 7468 |
rs765346277 | snp | A/C | 1.6741e-05 | 0.00289314 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938462 | ATAGAGAGACACAAT[A/C]ACTGACAAAACGGCC | 7468 |
rs765346560 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875365 | CGGCTCATTGCAGCC[C/T]TGATCACCTGGGCTC | 7468 |
rs765370368 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939134 | GGGAGGAGAGTGGCA[A/G]TGGCTCTGTTTTTCT | 7468 |
rs765376395 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943834 | TATCTTGAAAGGCTT[C/T]TGGTGAAAATGAAGG | 7468 |
rs765387218 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980759 | GCCACTGACTTGCTC[A/G]CGCGGCCGTGGCCTC | 7468 |
rs765407164 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965738 | GAAACTTACCATCAC[A/G]GTGAAGGTGAAGGGT | 7468 |
rs765410065 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930017 | GTTGGGGTGGGGCCC[A/G]GGAGTCTGCATTTCT | 7468 |
rs765457632 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969853 | AGGATTCAGAGATAG[C/G]CAGGCAGAAAGGAGA | 7468 |
rs765460349 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897982 | TGGGGAACTTTTGGA[C/G]GACCACTGTTTTCTC | 7468 |
rs765467450 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948230 | GGACGCGGGAAACAA[C/T]GGGAAAGTTCTTGAC | 7468 |
rs765475715 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981436 | TCAGCTTCAATCCTC[C/T]ATCATTAATGTGAAG | 7468 |
rs765493392 | in-del | -/CACTTGGTCCTTGCTGC | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947318 | TCTGGCCACAGGTGA[-/CACTTGGTCCTTGCTGC]CACCTGCTTGGGGCT | 7468 |
rs765503285 | snp | A/C | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981465 | AGCAAAACACAAAAA[A/C]CGCCCCAATCCCTCA | 7468 |
rs765507563 | snp | C/T | 2.39232e-05 | 0.00345847 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955677 | TAAGCCTGGCCGCCT[C/T]GCCCTCCTCTTGCAG | 7468 |
rs765528419 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897595 | GACTAGCCTGGTCAA[C/T]AAGACAAGATCCCGT | 7468 |
rs765533152 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891046 | CCACAGGCACATGCC[A/G]CCACGCCCAGCTAAG | 7468 |
rs765535552 | in-del | -/TT/TTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907615 | TACCTGTTGAATCTC[-/TT/TTT]TTTTTTTTTTTTTTT | 7468 |
rs765537179 | in-del | -/AAT | 1.64985e-05 | 0.0028721 | intron-variant, cds-indel | WHSC1 | GRCh38.p7 | 4:1939783 | CTGAGAATGAGGTAA[-/AAT]AATAATAATAACGAT | 7468 |
rs765554609 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952661 | ATGAAGACACAGTGT[C/G]ACCTTGAGCCTCAGT | 7468 |
rs765556921 | snp | C/T | 3.82512e-05 | 0.00437311 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974593 | CCTTGTTTGCCATCA[C/T]GGAGGATGCTGGGAG | 7468 |
rs765560629 | snp | A/G | 3.81127e-05 | 0.00436519 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955355 | GGTGAGGGGCCTGGG[A/G]GTGTCTGCGGCACAC | 7468 |
rs765651363 | snp | C/G | 1.6554e-05 | 0.00287693 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975040 | GCATGGGGCTCCTGG[C/G]TATGGGGGCAGAGTG | 7468 |
rs765662635 | snp | C/G | 1.66999e-05 | 0.00288958 | missense | WHSC1 | GRCh38.p7 | 4:1900714 | TGTAAAGTGCATAAA[C/G]ATGAAGCAGGCACCA | 7468 |
rs765670809 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951161 | TGTCTCATCCAAAAA[A/G]TCTGAGCGAGGAGTG | 7468 |
rs765680164 | snp | C/G | 3.30699e-05 | 0.00406618 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951254 | GTGTCTGACTGGGGC[C/G]CCGGTACGCAGAGCG | 7468 |
rs765708525 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908791 | TTGTTGTTGTTGTTT[C/T]GAGATAGGGTCTTGG | 7468 |
rs765718720 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973925 | CTGCTGGGTGGAGAT[A/G]TTGTCTCCAGTTCCT | 7468 |
rs765737954 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897161 | GGTGACAGAGTGAGA[-/CT]CTGTCTCAAAGGAAA | 7468 |
rs765748609 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923157 | AAATAAGCCAAACTA[A/G]TAACAGGCTATAAAG | 7468 |
rs765758911 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958413 | CCCCAAACACGTAGA[C/T]CCTGTACCTCAGAGA | 7468 |
rs765759709 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975313 | GGAGCTGACTTTTAA[C/T]TACAACCTCGATTGT | 7468 |
rs765760451 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960327 | ACTTTCCTCTGGGCT[A/G]GTAGCCAGGTGCTTG | 7468 |
rs765776797 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946851 | CCCGACAGGCCTCAT[C/T]TTTTTGGTTGGATAC | 7468 |
rs765786618 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880401 | CAGTCTATATGTGCA[C/T]GGAAGACTGAGCCAT | 7468 |
rs765836022 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909601 | ATGGGTCCTGTGAAG[C/T]CAGTACTTTTATATT | 7468 |
rs765853067 | snp | A/G | 1.68148e-05 | 0.0028995 | missense | WHSC1 | GRCh38.p7 | 4:1918516 | GACCCCAGAAGAGGA[A/G]TAGGGTCTCCTCCTG | 7468 |
rs765859258 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913189 | GAGCCCTCTGTCACG[C/G]CCAGACAGGGCCACT | 7468 |
rs765868871 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943807 | ATAAGCAGTCACCCA[A/G]AGTAAAGACTCTATC | 7468 |
rs765924252 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918920 | TGGGAGGCCAAGGCG[A/G]GAGGATTGCTTCAGC | 7468 |
rs765929015 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906912 | GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 7468 |
rs765969909 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888941 | CTCACTCTGTTGGCC[A/G]GGGTGGAGTGCAGTG | 7468 |
rs765979834 | snp | C/G | 0.0015438 | 0.0277402 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978952 | GGGGCGGTGCAGGGC[C/G]GCCGGCCCTGCCTGC | 7468 |
rs765998236 | snp | C/G | 1.64933e-05 | 0.00287165 | missense | WHSC1 | GRCh38.p7 | 4:1901094 | CCATTTGTGGTGACA[C/G]TGCTGCTGATGTGTC | 7468 |
rs766032332 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954327 | GGTTTCACCATGTTG[C/G]CCAGGCTGGTCTTGA | 7468 |
rs766062355 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957144 | CAGACCACAGGACAC[A/G]TCTAGGGTTGACATG | 7468 |
rs766081594 | snp | C/T | 1.65455e-05 | 0.00287619 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958052 | GTGGCGTGTGGGAGC[C/T]GCGTGCACGCGTGTG | 7468 |
rs766107492 | in-del | -/T | 1.67061e-05 | 0.00289011 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974801 | TTATGATGGTGAAAA[-/T]TCCCTTTAAAAATAA | 7468 |
rs766116822 | snp | C/G/T | 6.92681e-05 | 0.00588472 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901206 | GGAGCAGGGCCTTGT[C/G/T]GAAGCAGCTCTTGTG | 7468 |
rs766126997 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973461 | AGCACCGCGGCTCAG[C/T]GCGTCATGACAAAGC | 7468 |
rs766130939 | snp | C/T | 2.21202e-05 | 0.0033256 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953239 | GCCTCTGAAGAGGAG[C/T]TGCTTGATTTTAGTG | 7468 |
rs766132555 | snp | A/G | 3.35976e-05 | 0.0040985 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957900 | TTACCTGTATTTACT[A/G]AAATCTTTACTCCTA | 7468 |
rs766135979 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973305 | GCTGGTAATGGTAGG[A/G]ATGTAGGTTAGACAC | 7468 |
rs766138833 | in-del | -/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980918 | TGGAAGGTTGTTCTA[-/G]GGGACAGGCCGGGCA | 7468 |
rs766169100 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976398 | TGAAGTTCCTGGAGT[A/G]TAGCTCGCTCTTCTG | 7468 |
rs766187206 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953365 | GAGAGCAAGACAGAT[C/G]TTAAGCGCTGTGTGG | 7468 |
rs766200351 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945137 | CCCGCAGCTCTAGGG[A/C]GATCTGATTTTGTGT | 7468 |
rs766201120 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905485 | TGGTCTCTGGCTGGA[G/T]GCCTGAGCTCCTGTG | 7468 |
rs766214080 | snp | A/C | 8.60148e-05 | 0.00655744 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901200 | CTTGCTGGAGCAGGG[A/C]CTTGTCGAAGCAGCT | 7468 |
rs766246671 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965848 | AGAGAACTCACTCAC[C/T]GTCATGAGATGGCAT | 7468 |
rs766269612 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927107 | GTACCTTCTCTCACT[C/T]ATGCTGCTGGCAGGA | 7468 |
rs766275264 | snp | C/G | 8.51201e-05 | 0.00652325 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939612 | AGTAAAAAGATCAAG[C/G]GTTTATGATTTGAAA | 7468 |
rs766302782 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909679 | GGAGTCTTGCTCACT[C/T]GTCCAGGCTGGAGTA | 7468 |
rs766316131 | snp | A/G | 3.82416e-05 | 0.00437257 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974597 | GTTTGCCATCATGGA[A/G]GATGCTGGGAGCTCC | 7468 |
rs766371411 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977081 | CCAGAGGGGCCTGGC[C/T]TGGCTGCACTACAGT | 7468 |
rs766375297 | snp | C/T | 0.000354841 | 0.0133152 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916826 | TTGACTAGTTTCATC[C/T]CAGATTCTAACTTTC | 7468 |
rs766410762 | snp | A/G | 1.65452e-05 | 0.00287616 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900729 | GATGAAGCAGGCACC[A/G]GAAATCCTCGGCAGT | 7468 |
rs766420534 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908654 | GAGGAGCTTATGTGT[C/T]AGCTGACCCACCCCT | 7468 |
rs766466000 | snp | C/T | 0.000116265 | 0.00762357 | missense | WHSC1 | GRCh38.p7 | 4:1918219 | GAAGCTGCAAGCATG[C/T]CAGTGGAGGAGCGGA | 7468 |
rs766477164 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1975346 | GGGCAATGAAAAAAC[A/G]GTCTGCCGGTGTGGA | 7468 |
rs766496762 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961747 | CTGACAGGTGTTGCC[G/T]GGCCCTTCCAGGGCG | 7468 |
rs766501861 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910569 | AGATTTTTGTTGTCA[C/T]CTTTTCTGTGTTATG | 7468 |
rs766506735 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870551 | CCGCTCGCCCGCGCC[A/G]CTTCCTCCTCCTCCC | 7468 |
rs766536410 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904848 | CATATTAAGAATGTA[C/T]GGCCGGGCACGGTGG | 7468 |
rs766541026 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958558 | CCTCAGGGCTGCCTG[C/T]GCTCAGAGCTGGTGC | 7468 |
rs766541251 | in-del | -/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947014 | TCAAGAAATGACTGA[-/G]GGTAGGGGTGGGGGT | 7468 |
rs766542595 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974090 | CTCAGCCAACGCCAC[A/T]TCAGCGCCATGGGTG | 7468 |
rs766544960 | snp | C/T | 4.63446e-05 | 0.00481354 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955679 | AGCCTGGCCGCCTCG[C/T]CCTCCTCTTGCAGGG | 7468 |
rs766646098 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | WHSC1 | GRCh38.p7 | 4:1900839 | TGCAGGAGGGGGTCA[C/T]GCAGAAGTTTAACGG | 7468 |
rs766657490 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947083 | AGTGGAAGCAGGTGT[A/G]TTGTGGGCAGTTTTG | 7468 |
rs766667797 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878573 | TTGCTGTCATGTCCT[C/T]AGCACCTGGAATGGT | 7468 |
rs766672132 | snp | A/C/T | 3.40236e-05 | 0.00412442 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952060 | TTGTGGTAAGAGGTG[A/C/T]AGAAGGGACTGCCGG | 7468 |
rs766678634 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939313 | TATGTAAGACTTTAT[A/G]TTTAGAGATTTGTGC | 7468 |
rs766703290 | in-del | -/TTTTC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896776 | TCTTTCTTCTCTTTT[-/TTTTC]TTTTCTTTTCTTTCT | 7468 |
rs766713533 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886898 | ATTGATATATGTTCA[A/G]TTCTATCTGTGGAAG | 7468 |
rs766717444 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951181 | AGCGAGGAGTGACTG[C/T]CAAAAAGGAGTATGT | 7468 |
rs766736390 | snp | A/G | 0.000231892 | 0.0107653 | missense | WHSC1 | GRCh38.p7 | 4:1904370 | TTCACAGCTATACCA[A/G]ACTTAAAGGTATTGT | 7468 |
rs766759466 | snp | A/G | 1.64942e-05 | 0.00287173 | missense | WHSC1 | GRCh38.p7 | 4:1904246 | GAGTCTTGTCCAAAC[A/G]CTGGAAGAGACAAAG | 7468 |
rs766764224 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923447 | GAGCCAGTAAGTGCA[C/T]GAAGAGATGCTGCTC | 7468 |
rs766766326 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940327 | GTGTTGAGGTGAGTC[A/G]GAACTACCATTGTAA | 7468 |
rs766815181 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965391 | TGTGGGCTACCACCA[A/C]GCAGACCAATATATC | 7468 |
rs766823101 | snp | A/G | 0.000131733 | 0.00811476 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976446 | TGTGTAATTCTTTCC[A/G]GTGATCTGTGCTTAA | 7468 |
rs766839219 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967252 | AATCTGAATAGACTT[-/A]ATAACTAGTAGAGAG | 7468 |
rs766849084 | snp | A/G | 1.65861e-05 | 0.00287972 | missense | WHSC1 | GRCh38.p7 | 4:1935153 | TCCAAGGTAATGTAA[A/G]TGGGAAAAAAAGAAA | 7468 |
rs766871047 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963139 | ATGACAGATAAGGGG[A/C]CTGAGCTTGCTAAGT | 7468 |
rs766875306 | snp | G/T | 1.64751e-05 | 0.00287007 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959707 | GACAGATGGCAAAGG[G/T]TGGGGCCTGGTCGCC | 7468 |
rs766885488 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949379 | TTTAGACTTTGTGCT[C/G]TCAGGAGATGTATCT | 7468 |
rs766889793 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970019 | GAGCAGAGTGCAGCT[A/G]AAAGAACCTGGGAAA | 7468 |
rs766891258 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926231 | ATGATCTCGGCTCAC[G/T]GCAACCTCCGTCTCC | 7468 |
rs766904018 | snp | A/C | 3.44353e-05 | 0.00414927 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930818 | TGGGTTGATGTGTGT[A/C]GTGTAGCAAGCTGAG | 7468 |
rs766946616 | in-del | -/AT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884539 | GCTGGGATTACAGAC[-/AT]GTGCCACCACGCCTA | 7468 |
rs767005728 | in-del | -/GATGCATGGGA | 1.65765e-05 | 0.00287888 | frameshift-variant, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952219 | GGTTCACCTGCAGCG[-/GATGCATGGGA]AGTGTGCCTCAGGCA | 7468 |
rs767034741 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901116 | TGATGTGTCTCAGTC[A/G]GAAGAAAATGGACAA | 7468 |
rs767051577 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880356 | CCTGGGAACTTACTT[-/T]GTTTTGCCTCTTGGA | 7468 |
rs767056481 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906957 | TGAGCCACCGTGCCC[A/G]GCCTCATCTCTCTTT | 7468 |
rs767063335 | snp | A/G | 0.000207709 | 0.0101888 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930616 | ATTGCACCTTCTCCC[A/G]TTCCCACAGGTGGTA | 7468 |
rs767082089 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883492 | CAAAAAATAGCTGGG[C/T]GTGGTGGCGCACACC | 7468 |
rs767099837 | snp | A/T | 0.000119549 | 0.00773047 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904180 | ACAGGTAGTGATTGG[A/T]TGTGTTAGTGTTTGT | 7468 |
rs767126550 | snp | C/G | 1.64966e-05 | 0.00287194 | missense | WHSC1 | GRCh38.p7 | 4:1978720 | CTGCCCCAATTCGTT[C/G]TGTAAGGAGCACCAG | 7468 |
rs767136511 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922154 | TTCGTCTCCAAGAAA[A/G]TACTAGCCAGTATTA | 7468 |
rs767174285 | in-del | -/TG | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980582 | GCTACTCCGTGGTTT[-/TG]TGACCTGTAAGCGTG | 7468 |
rs767179735 | snp | A/G | 5.34412e-05 | 0.00516892 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976698 | GGTGTGCAGCCTCGC[A/G]GTGGCTTGCAGCTGT | 7468 |
rs767215238 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945321 | GGGAGGATGCTGTGT[A/G]AGAGCCATGCTGTCA | 7468 |
rs767215453 | snp | A/G | 1.70252e-05 | 0.00291759 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959467 | GCTTACTCCTTCCCT[A/G]CAGGTGAATAAGCCT | 7468 |
rs767219774 | in-del | -/CTTAA | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982199 | TTTAAAGGCTTTTTT[-/CTTAA]CTTATTTTATATGGG | 7468 |
rs767234783 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912309 | TTGAACTCTTCAGCC[A/G]TTTTCTATTTCTTTC | 7468 |
rs767239709 | snp | G/T | 1.64795e-05 | 0.00287045 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953410 | AAATTTTACCATGAG[G/T]CTTGTGTGAAAAAAT | 7468 |
rs767281226 | snp | C/T | 1.65636e-05 | 0.00287776 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978783 | GCGGTCCTACTGCTG[C/T]GAGCATGACTTAGGG | 7468 |
rs767292520 | snp | C/T | 1.98387e-05 | 0.00314944 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953256 | GCTTGATTTTAGTGG[C/T]TCAGAACTGCAATTT | 7468 |
rs767299529 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900750 | CCTCGGCAGTGCCAA[C/T]GGGAAGACTCCGAGC | 7468 |
rs767322037 | in-del | -/TTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881720 | ATTATTCTCTCCACA[-/TTT]TTTATATGTGTTTAG | 7468 |
rs767322960 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904004 | CTCCCAAAGTGCTGG[A/G]ACTACAGGCGTGAGC | 7468 |
rs767359725 | snp | A/G | 1.90831e-05 | 0.00308888 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974608 | TGGAGGATGCTGGGA[A/G]CTCCAGCTCCCTGTC | 7468 |
rs767370639 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892063 | TAGCACCTCAAGAAT[A/G]AGGAAGGCATTTTGT | 7468 |
rs767374130 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937297 | GACCTCAAGTGATCC[A/G]CCCACCTCCACCTCC | 7468 |
rs767388620 | snp | C/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870606 | CACCCCCTGAAGCCC[C/G]GCTCTACCGCAGCGG | 7468 |
rs767403521 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981535 | CCATACCCACCCGTG[C/T]GCGCCCACAGGGGGA | 7468 |
rs767417151 | snp | A/T | 1.65002e-05 | 0.00287225 | intron-variant, stop-lost | WHSC1 | GRCh38.p7 | 4:1939787 | GAATGAGGTAAAATA[A/T]TAATAATAACGATAA | 7468 |
rs767419049 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914518 | TTTAGTAGAGACAGG[G/T]CTTCACCATGTTGGC | 7468 |
rs767422079 | snp | A/G | 1.65086e-05 | 0.00287298 | missense | WHSC1 | GRCh38.p7 | 4:1918363 | GTCAGTGAAGAAGCT[A/G]CTGAAAACCCCAAGT | 7468 |
rs767440358 | snp | A/G | 3.30945e-05 | 0.0040677 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955867 | GTGAGACATAGAATC[A/G]TATGCTTTTATGTCT | 7468 |
rs767440951 | in-del | -/A | 1.83397e-05 | 0.00302812 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900615 | TTTTTTCTTTTTTTT[-/A]AATACCATAGTGTTC | 7468 |
rs767449236 | snp | A/G | 1.78793e-05 | 0.00298987 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974667 | GGTCCTCTCCACGTG[A/G]TCCTGACCTGTCCTC | 7468 |
rs767465642 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909135 | TGTCCCAAATTTGAC[C/T]AGTGGGAGTTCTATT | 7468 |
rs767478314 | in-del | -/CTC | 0.000115474 | 0.00759762 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975279 | CAATTTGGTGTCTGT[-/CTC]CTCTTCTCCCAGGGA | 7468 |
rs767481872 | snp | A/C | 1.65414e-05 | 0.00287583 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952158 | AGGACCCTGCTGCGG[A/C]GCTTTCCACCTCGCC | 7468 |
rs767499356 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967332 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 7468 |
rs767564829 | in-del | -/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943818 | CCAAAGTAAAGACTC[-/T]TATCTTGAAAGGCTT | 7468 |
rs767569743 | snp | A/G | 1.65332e-05 | 0.00287512 | missense | WHSC1 | GRCh38.p7 | 4:1935164 | GTAAATGGGAAAAAA[A/G]GAAACCACACAAAGA | 7468 |
rs767612734 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959719 | AGGGTGGGGCCTGGT[C/T]GCCAAGAGGGACATC | 7468 |
rs767624559 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975482 | GTCCCCCGTGAACAG[C/T]GGCTTCCTCCAGGCT | 7468 |
rs767627490 | snp | C/T | 1.6646e-05 | 0.00288491 | missense | WHSC1 | GRCh38.p7 | 4:1956099 | AAGATTATTACTGGA[C/T]GCATCAGGCGCGAGT | 7468 |
rs767640915 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963328 | TGCTCAAAGGCTTGG[C/T]GGCCAACTGGAGTTG | 7468 |
rs767641930 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901279 | CGTTGTGTAAGGGGT[C/T]ATGTGACCTTGAGCA | 7468 |
rs767653275 | snp | A/G | | | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939738 | CAGCTCTTGGGTTTA[A/G]CAAAAGTTCATCTCC | 7468 |
rs767663779 | snp | A/G | 2.24253e-05 | 0.00334845 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976467 | CTGTGCTTAATTCTT[A/G]ACTCTAGACCTCGAC | 7468 |
rs767679424 | snp | A/C | 5.09247e-05 | 0.00504577 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952064 | GGTAAGAGGTGCAGA[A/C]GGGACTGCCGGGCGC | 7468 |
rs767701479 | snp | C/T | | | missense | WHSC1 | GRCh38.p7 | 4:1918505 | CGGCAGAGGCTGACC[C/T]CAGAAGAGGAGTAGG | 7468 |
rs767728008 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899406 | CAGAGGTCAGGGTCC[A/G]CCCCCTAGTGGTGGT | 7468 |
rs767759086 | snp | C/T | 6.15795e-05 | 0.00554851 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976579 | GTCAGAGGACGAGTG[C/T]TTCCGCTGCGGTGAT | 7468 |
rs767761849 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1890712 | GTTCCAGTGGTTCTA[C/T]CTCAGCCTCCCAAGT | 7468 |
rs767802642 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876569 | TGGTGGTGTGTGCCT[A/G]TAGTCCCAGATACTT | 7468 |
rs767888998 | snp | A/G | 3.04113e-05 | 0.00389932 | missense | WHSC1 | GRCh38.p7 | 4:1978880 | AGGCGGCGGCGGAGG[A/G]GCTGGCGGAGAGTCA | 7468 |
rs767900503 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874716 | CTGTACTACCACCAA[A/G]ATGGAGCAAGAAATC | 7468 |
rs767916164 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925674 | AAAGTCCTGGGATTA[C/T]AGGCCTGAGCCACTG | 7468 |
rs767929593 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980357 | GCCCACGTGTCCTGA[G/T]GGGCTGCTTGTCTGG | 7468 |
rs767934476 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956768 | GGCCAGTAGAGAAAA[-/C]CCCGAGGTGTGTGCA | 7468 |
rs767961646 | snp | C/T | 9.89071e-05 | 0.00703163 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916917 | ACAGTTCTTTGGTGA[C/T]GCCCCAGAAAGAGCT | 7468 |
rs767973030 | snp | A/C | 1.66818e-05 | 0.00288802 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955309 | ACACCACGCCCACGT[A/C]AACGTGAGCTGGTGC | 7468 |
rs767981389 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933646 | TGATCCACCCACCTC[A/G]GCCTCCCAGAGTGCT | 7468 |
rs767992645 | snp | C/T | 1.67385e-05 | 0.00289292 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959792 | TTACGGTTCACTGGG[C/T]AATTAGGCCTAGGTT | 7468 |
rs767998808 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979570 | TCTCCTCATGGATTT[A/G]AATGAAATGCCAATA | 7468 |
rs768014556 | snp | C/T | 1.6773e-05 | 0.0028959 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904405 | TTTGGGTTGTTTTTC[C/T]AACTTTCTCTTCTGC | 7468 |
rs768024031 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | WHSC1 | GRCh38.p7 | 4:1935206 | CCTACAGAAGATGCT[A/G]AAGCTGAGGACACAC | 7468 |
rs768024193 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958582 | CTGGTGCGGCAAGCC[G/T]CATCCCCAGGAGCCT | 7468 |
rs768026160 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935480 | TGTTATCACAGAAAC[C/G]GATGGTGTGTTGCTC | 7468 |
rs768047388 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957548 | CTGCCTCGGCCTCCC[A/G]AAGTGCTTCGATTAC | 7468 |
rs768087427 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978584 | TCAACCACGATAATG[C/T]TGAAGTCGTGATTCC | 7468 |
rs768102024 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889505 | CGGCCAAGATTTGAC[-/T]TTTTTTTTTTTTTGA | 7468 |
rs768109486 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967315 | CCGGGCACGGTGGCT[C/T]ATGCCTGTAATCCCA | 7468 |
rs768111126 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888649 | GGCTTACTGCGGCCT[C/T]CACCTCCAGGGTTCA | 7468 |
rs768143940 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964521 | TCGCACACAGCTTGA[A/G]GGGTTCAGGGTGAGC | 7468 |
rs768176608 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877602 | GTCTCAGCTTGGGCC[C/T]CACACTGAATGCTGT | 7468 |
rs768184951 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | WHSC1 | GRCh38.p7 | 4:1904312 | TGGTCCAAAGTGTCG[C/G]GTTACCCTTGGTGGC | 7468 |
rs768205892 | snp | A/T | 1.65943e-05 | 0.00288043 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959764 | CGTTATCCCCTCCCC[A/T]GCTTTTGAGAAATTA | 7468 |
rs768215604 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898980 | TCTCAGTTCCTTCAG[A/G]AGGTGGTTTTTTATG | 7468 |
rs768231623 | snp | C/G | 1.66713e-05 | 0.0028871 | missense | WHSC1 | GRCh38.p7 | 4:1935144 | ATTCCCCATTCCAAG[C/G]TAATGTAAATGGGAA | 7468 |
rs768239278 | snp | A/C | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949194 | GAGCACGTCAAGTGG[A/C]CCTTTGTGGGTGTTA | 7468 |
rs768246858 | snp | A/C | 4.97954e-05 | 0.00498951 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916867 | ATTTTATTTTAAAAA[A/C]TAGGTCAGAAAAAGA | 7468 |
rs768257443 | snp | C/T | 1.6788e-05 | 0.00289719 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961014 | CGCTTTTTGTCATGG[C/T]CACATGCTTGTGATT | 7468 |
rs768271090 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979863 | AGGAGTGACTTTGCA[A/G]GGCGTGAGACCGCAG | 7468 |
rs768275016 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920112 | GATTTTTTTGTCCCT[A/G]TATGGGATCTGGAAA | 7468 |
rs768306892 | snp | A/G/T | 3.33663e-05 | 0.00408439 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952244 | CAGGCAAGTTCCCAC[A/G/T]GGCGGGCAGCTCTGC | 7468 |
rs768310333 | snp | C/T | 3.52131e-05 | 0.00419587 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976695 | GTGGGTGTGCAGCCT[C/T]GCGGTGGCTTGCAGC | 7468 |
rs768335082 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910371 | GCTGGCACTACAGGC[A/G]TGTGTCACCACACCC | 7468 |
rs768350264 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961347 | TAGAGCTAACCACCT[C/G]TCAGCACCCAGGCAC | 7468 |
rs768365154 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906310 | GTGGCGCAGTCTTAG[C/T]TCACTGCAACCTGTA | 7468 |
rs768390477 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956916 | GCTTTGCAGGCTGCA[C/T]TGAGTGGTAGGAGTG | 7468 |
rs768444159 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905164 | TTATATGTCCCTGAT[A/C]CAGAGCAAATAATGG | 7468 |
rs768489379 | snp | A/G | 1.67478e-05 | 0.00289372 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951037 | CCGCTGTGTTCTGCG[A/G]CTAGTGAACTGTCAT | 7468 |
rs768498399 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950632 | TGAGGCTGACACTTA[A/C]TTCATCTGTGGTTCC | 7468 |
rs768565646 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922543 | AGGAATTTATTTGCC[C/G]TTTGTAAGTGGATGC | 7468 |
rs768581055 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970617 | CACCCCCAACACCGG[C/T]GAGCCAGAGCCGCTG | 7468 |
rs768587630 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887895 | AGTTACACTAGATCT[G/T]TCAGTTCCTTTTTTT | 7468 |
rs768622257 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979370 | GTGAGGCCCGTGTGA[G/T]GACTGACCCTGGATT | 7468 |
rs768660174 | snp | A/G | 1.70455e-05 | 0.00291933 | missense | WHSC1 | GRCh38.p7 | 4:1918589 | GAGATGCAGCATCCC[A/G]GTTTTTGGTCTTCTG | 7468 |
rs768675844 | in-del | -/AG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965709 | ACAGTTCCACATAAC[-/AG]GGGAGGCCTCAAGAA | 7468 |
rs768690505 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1950014 | TAACATAATTACTTG[G/T]TTTTGTGATGATTGA | 7468 |
rs768709494 | snp | C/T | 1.77329e-05 | 0.0029776 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959423 | GTGTGCAAGGGTATT[C/T]GGAAGGCTCTCATGT | 7468 |
rs768710163 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918764 | TCTAATAAATAAGTA[C/T]TAGGGAACAGCCATT | 7468 |
rs768722202 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915734 | CCATTGACCACTTAA[C/T]TGGGGGAATCTCCAG | 7468 |
rs768776650 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934358 | CCAAAGTATTGGGAT[C/T]ACAGGCATGAGCCAC | 7468 |
rs768786877 | in-del | -/A | 0.000279004 | 0.0118078 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938442 | TTTTTTTTTTTTTTT[-/A]AATAATAGAGAGACA | 7468 |
rs768805284 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967043 | TAGATGGACTAGGAA[A/G]AAAAGAGAAAAGACT | 7468 |
rs768831620 | snp | A/G | 6.64871e-05 | 0.00576534 | missense | WHSC1 | GRCh38.p7 | 4:1901166 | GAAGGAACAGGAAGA[A/G]GAGCATAAAATATGA | 7468 |
rs768846522 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945925 | ACACTTCTCTAACAT[C/G]TAGCCCTTTTAAATT | 7468 |
rs768855129 | snp | A/T | 0.000175221 | 0.00935841 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938442 | TTTTTTTTTTTTTTT[A/T]AATAATAGAGAGACA | 7468 |
rs768871474 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896494 | ACACCTCAGCCTCCC[A/G]GGTAGCTGGGACTGT | 7468 |
rs768921269 | snp | C/T | 1.65507e-05 | 0.00287664 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938546 | AGGTAATGTGGTCAG[C/T]GCCCTTTCCTTCTTG | 7468 |
rs768946707 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923039 | CTGCAGGCCAGTTGC[C/G]TGGGAGGTCTGCACT | 7468 |
rs768972964 | snp | C/T | 6.61759e-05 | 0.00575183 | missense | WHSC1 | GRCh38.p7 | 4:1978683 | ACGTGTGTGGCAAAC[C/T]TTCGACTTCATTTTG | 7468 |
rs768992336 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929852 | AGGCCAGACCCGGTG[G/T]GTTGGGTTGATCTTG | 7468 |
rs769003528 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977702 | AAATGCTTGAACCCG[C/G]GAGGCGGAGGTTGCA | 7468 |
rs769003652 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965605 | GCTACTCATTACATG[C/T]AAGGTGTATTAGTCT | 7468 |
rs769010945 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953541 | TACAGGTGCACCTGC[A/G]CAGCCTTGCTGTGGG | 7468 |
rs769026668 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924411 | TGCTCGGCTGTGTCT[C/T]TACAACCTGTTCACT | 7468 |
rs769083033 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946494 | CAGGCTGGTCTTGAA[C/T]TCCTGACCTCGTGAT | 7468 |
rs769097178 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938895 | TGTCACCCTTCAGTA[C/T]CCTGACCCTCTGCAT | 7468 |
rs769134322 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892541 | TCTTCCCACCTCTGT[C/T]CCTGTCCCCCTTAGA | 7468 |
rs769162551 | snp | G/T | 3.30044e-05 | 0.00406216 | missense | WHSC1 | GRCh38.p7 | 4:1916990 | CAGTTTGAAAAATTA[G/T]GCCAGGAAAGTGCCA | 7468 |
rs769163692 | snp | A/G | 1.66247e-05 | 0.00288307 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955799 | TGACTGCAGGGCTGG[A/G]AAGAAGCTGCACTTC | 7468 |
rs769203933 | snp | C/G | 3.30562e-05 | 0.00406534 | missense | WHSC1 | GRCh38.p7 | 4:1978761 | CCTTCAGCTGCACCC[C/G]GGACGGGCGGTCCTA | 7468 |
rs769207647 | snp | A/G | 3.37815e-05 | 0.0041097 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961185 | GTGAGCTTCTGCAGT[A/G]TGCTGGACCTGGAGC | 7468 |
rs769213407 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874478 | GCATTGCCTCTGCTG[G/T]TGCATTCTCATGGCA | 7468 |
rs769235694 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970776 | GCAGGGACATGTAAT[A/G]TCCGGGACATTACAT | 7468 |
rs769251478 | snp | A/C | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869818 | CACTGGCCTTGGCTC[A/C]ATTTTGAATTAATTT | 7468 |
rs769268150 | snp | A/G/T | 3.30553e-05 | 0.00406531 | synonymous-codon, missense | WHSC1 | GRCh38.p7 | 4:1918299 | TCAAGTAGCCAAGGA[A/G/T]GCTGGCATTGCTGCA | 7468 |
rs769268489 | snp | C/T | 0.000249603 | 0.0111687 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951054 | TAGTGAACTGTCATC[C/T]GCCTCCTTCATCTCT | 7468 |
rs769280128 | snp | C/T | 1.68029e-05 | 0.00289848 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961169 | AATGCGGAACTCCAC[C/T]GTGAGCTTCTGCAGT | 7468 |
rs769283882 | snp | C/T | 1.66181e-05 | 0.00288249 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955303 | GAAGCGACACCACGC[C/T]CACGTCAACGTGAGC | 7468 |
rs769299013 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906892 | TCTCAAACCTCTGAC[C/T]TCAAGTGATCTGCCC | 7468 |
rs769304257 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889481 | ATTATGGGTGTGAGG[C/T]ACCACGCCCGGCCAA | 7468 |
rs769307674 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902828 | CTTCCTCTGGAGAGT[-/G]GGGTCAATAAATGTA | 7468 |
rs769316138 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943404 | CCTGTTGTGACAGTA[A/G]TAATGGTTATAATAA | 7468 |
rs769335181 | snp | A/G | 3.34208e-05 | 0.0040877 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961020 | TTGTCATGGCCACAT[A/G]CTTGTGATTTCCAGG | 7468 |
rs769344595 | in-del | -/T | 5.70912e-05 | 0.0053425 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974616 | GCTGGGAGCTCCAGC[-/T]CCCTGTCCTGTCCTC | 7468 |
rs769348800 | snp | C/G | 1.70778e-05 | 0.00292209 | missense | WHSC1 | GRCh38.p7 | 4:1900695 | CCCTTTCTGTTCAGA[C/G]TGTTGTAAAGTGCAT | 7468 |
rs769354613 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979446 | CTGTATCATTTTTTT[C/G]TACTAATGTGAATTG | 7468 |
rs769370254 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935962 | AAGTCCATTAGAGAT[A/G]TGTGTTACATGTCAA | 7468 |
rs769373851 | snp | C/T | 2.32151e-05 | 0.0034069 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955385 | CGCCTCTCACACTCC[C/T]AGGAGCCACATATCA | 7468 |
rs769376398 | snp | A/C | 1.65291e-05 | 0.00287476 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916887 | TCAGAAAAAGAGTGC[A/C]CGCCAGTATCACGTA | 7468 |
rs769386592 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980106 | GGTCCTGGGGGTGGA[A/G]GCCTGCCTGGCAGGT | 7468 |
rs769395256 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950370 | GGCCTTTTACCTAGA[C/T]TCAGATGTGAATCAA | 7468 |
rs769460039 | snp | A/G | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949275 | CAGTGACAGAGCCTT[A/G]AAGTGTGCACTGCTC | 7468 |
rs769461311 | snp | C/T | 0.000547895 | 0.0165423 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938422 | TTTTTCTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs769482261 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899336 | CGCATAGCCCTGTTG[C/T]GCGGGCATCCTGTGC | 7468 |
rs769541254 | snp | C/T | 0.000876168 | 0.0209121 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978929 | AGGCGGCCGCTTGGC[C/T]GGATCCAGGGGCGGT | 7468 |
rs769541514 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945053 | CCTTGGACAGGAGTC[A/G]GGGGCTCCTCTGTCC | 7468 |
rs769597310 | snp | C/G | 1.80732e-05 | 0.00300604 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930595 | GTTTTACGGATTTAA[C/G]TTCTCATTGCACCTT | 7468 |
rs769628530 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978374 | GACACTCCTGCACCC[A/G]GCACAGCTCCTCTCA | 7468 |
rs769664251 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927284 | ACCATTTCTGCACTA[G/T]GTTATTGACTACGCC | 7468 |
rs769675903 | snp | C/T | 1.65307e-05 | 0.0028749 | missense | WHSC1 | GRCh38.p7 | 4:1930744 | AGTTTGCCCTGGTGG[C/T]CCCTGTCCAGGCTGA | 7468 |
rs769697116 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907892 | ATTACAGGCATGAGT[C/G]ACTGTGCCTAGCCTC | 7468 |
rs769709812 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876076 | AAAAATAAGCTGGGC[A/G]TGGTTGCAGTGCCTG | 7468 |
rs769716037 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892411 | TATAGGGGCTGTTCA[A/G]CCTCCCTAGCCCCTT | 7468 |
rs769738388 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958296 | ACAGTCCTGACCGGG[C/G]TGCTTGGAGCAGGAG | 7468 |
rs769777776 | snp | A/C | 1.64963e-05 | 0.00287192 | missense, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975002 | TCTGTGACATTCCTG[A/C]AGGTACAAGCTCTGG | 7468 |
rs769782258 | snp | A/C/T | 0.000247817 | 0.0111289 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958041 | AGCACATCAAGGTGG[A/C/T]GTGTGGGAGCTGCGT | 7468 |
rs769788717 | in-del | -/ACA | 5.13272e-05 | 0.00506567 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974755 | ACCACGGTTTTCAGT[-/ACA]ACAAGGAACACAACT | 7468 |
rs769797204 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904742 | AATTTTATTAGGCCT[A/G]TGGGAAGAATGGAAA | 7468 |
rs769815661 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953340 | GATTCACTCATGTTT[C/T]GTGTGTAAAGAGAGC | 7468 |
rs769824788 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923699 | CTTTTTTTCTCTTAC[A/G]GTTTTACTCCTAGAT | 7468 |
rs769833708 | in-del | -/GTGA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881899 | TCCATGAGGGTGGGG[-/GTGA]GTGAGTATCAGATGG | 7468 |
rs769847962 | snp | C/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870388 | GCCGAAGGTGTTCCC[C/G]GCTCCCTGAACCTGC | 7468 |
rs769849406 | in-del | -/GA | 1.65965e-05 | 0.00288062 | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1978888 | GCGGAGGGGCTGGCG[-/GA]GAGTCACAGAGGGCA | 7468 |
rs769864258 | snp | C/T | 1.66131e-05 | 0.00288206 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938573 | CTTGGCTTCTGGGTG[C/T]CCAGGCTGGGCTGGG | 7468 |
rs769866382 | snp | G/T | 1.65203e-05 | 0.002874 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975259 | AAGAGAAAGGCAGGT[G/T]TTTCCAATTTGGTGT | 7468 |
rs769868346 | snp | C/G | 1.69622e-05 | 0.00291219 | missense | WHSC1 | GRCh38.p7 | 4:1978818 | CATCGGTCAGAAGCA[C/G]CAAGACTGAGAAGCC | 7468 |
rs769888096 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906482 | TGGGCCCCAGTGATC[C/T]GCTTGCCTCGGCCTC | 7468 |
rs769890175 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921698 | GAGAAAGGAGAATCG[C/G]TTGAACCTGGGAGAC | 7468 |
rs769903452 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967073 | TCACATAACTAAAAT[C/G]AGAACTGGGTGTGTG | 7468 |
rs769906407 | snp | A/G | 6.85953e-05 | 0.00585602 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1901197 | CTCCTTGCTGGAGCA[A/G]GGCCTTGTCGAAGCA | 7468 |
rs769919064 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892590 | TTTTTTTTTGAGACG[G/T]AGTCTTGCCCTGTCG | 7468 |
rs769930210 | snp | A/G/T | 1.68332e-05 | 0.00290109 | missense | WHSC1 | GRCh38.p7 | 4:1918520 | CCAGAAGAGGAGTAG[A/G/T]GTCTCCTCCTGGGAG | 7468 |
rs769942097 | snp | A/G | 1.66596e-05 | 0.00288609 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918197 | AATGGGCATTGTTCA[A/G]GCAGAAGAAGCTGCA | 7468 |
rs769950208 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939710 | CGAAATCGGGCTTCC[A/G]CGGCAGCATCTTCAG | 7468 |
rs769959332 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955421 | GGCTCATTCCTTGTC[C/T]GCGCTGTGTTCATTG | 7468 |
rs769963847 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954368 | CACTGCTCTGACCTC[-/TT]TTCTTTTTTTTGAGA | 7468 |
rs769993981 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910501 | TTTAGATATTACACT[C/T]ACTGGTCTCTTTAGG | 7468 |
rs769998259 | snp | A/G | 3.71368e-05 | 0.00430894 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901294 | CATGTGACCTTGAGC[A/G]GTGAGCATGGCCACC | 7468 |
rs770028586 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | WHSC1 | GRCh38.p7 | 4:1900817 | AAAGCCCAGCTCTCC[A/G]GTAGCCTGCAGGAGG | 7468 |
rs770066164 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883591 | AGCCCAGATTACACC[A/C]CTGCACTCCAACCTG | 7468 |
rs770070191 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968838 | TGCACGTCCGACAGT[A/T]GGAAAGATCCTAAAG | 7468 |
rs770096134 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962965 | CAGCACATTCCTCTC[A/C]GGGCCCTGTCAACAC | 7468 |
rs770123143 | in-del | -/AT | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942859 | CTCATTGCCAGTGAG[-/AT]ATATTCAGTATTGTA | 7468 |
rs770137606 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926433 | GCTGCGATTACAGGT[A/G]TGAGCCACCGTGCCT | 7468 |
rs770139864 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937606 | ACCACATATGACACC[C/T]AATGTGCACTGAGCA | 7468 |
rs770157005 | snp | C/T | 0.00014422 | 0.00849052 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953574 | CAGATGCAGGCCAGA[C/T]GCAGGCCCATGGGCG | 7468 |
rs770171601 | snp | A/G | 1.65157e-05 | 0.0028736 | missense | WHSC1 | GRCh38.p7 | 4:1918333 | TCTTTGGGAGAAATG[A/G]CAGAATCCTCAGGAG | 7468 |
rs770225758 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911711 | TAAAAACAGTGAGAT[A/G]TTCACCTCTCAACTT | 7468 |
rs770228176 | in-del | -/A | | | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974843 | AACACTTGACCGAAT[-/A]ATATCACTTGACCTT | 7468 |
rs770255988 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893451 | CAGTTCCAGCCTGGG[C/T]GACAGAGACTCCGTT | 7468 |
rs770268966 | snp | C/T | 1.6628e-05 | 0.00288335 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955953 | TGTCTCTGAGGAGTC[C/T]GTGAATCCTGTTTTT | 7468 |
rs770269970 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924712 | GGTTGGTAGTTTGAG[A/G]ACAGCCTGGGCAACA | 7468 |
rs770283325 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881553 | CAGGCGTGAGCCACC[A/G]TGCCTGGCTTGTTTT | 7468 |
rs770290363 | snp | C/G | | | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975183 | CCATGGGTCAAGCCA[C/G]TACAGATACAAAAAT | 7468 |
rs770313408 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884802 | TCTGAAATCTGCAAG[C/T]GTGTCTTTAAAATTC | 7468 |
rs770343907 | in-del | -/GCCCTG | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945361 | TGCTGCTCCTGTGCT[-/GCCCTG]GCCCTGGCCCTGGCC | 7468 |
rs770344025 | snp | C/T | 0.000220614 | 0.0105004 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955766 | CATCGAGATGCCTGA[C/T]GGCAGCTGGTTCTGC | 7468 |
rs770355147 | snp | A/G | 1.66366e-05 | 0.0028841 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952110 | TCTGCCCCCGCAGCT[A/G]TGTGAGAAGCCGGGC | 7468 |
rs770376132 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899487 | TCCCCATTTGAGAAC[C/T]GCTGTTCTAGTCCAC | 7468 |
rs770394348 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876325 | ACTTTCTGTAATACT[G/T]AGTGGTTTCAACAAA | 7468 |
rs770395467 | snp | A/G | 3.29843e-05 | 0.00406092 | missense | WHSC1 | GRCh38.p7 | 4:1900880 | CTGCCCTTTATTCCA[A/G]CCGACAAGCTGAAAG | 7468 |
rs770405964 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1940193 | AAGGCGACTCACACA[C/T]CACACCTGATTCCTG | 7468 |
rs770424894 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891478 | AGTTGGATTCACGGA[A/G]TTATCAGAGTGGGCT | 7468 |
rs770425230 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951111 | CCCTCGGAGTCCCCA[C/T]ACGAAAGTGCAGACG | 7468 |
rs770428055 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941698 | TCCTTATATGAAAAC[G/T]TTTAAATTACTGGGT | 7468 |
rs770431667 | snp | C/T | 1.77546e-05 | 0.00297943 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930605 | TTTAACTTCTCATTG[C/T]ACCTTCTCCCGTTCC | 7468 |
rs770455266 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972810 | GACATTGTGCACGGA[A/G]GATTCCATTGGGAGC | 7468 |
rs770491529 | in-del | -/AAAC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935867 | TTCTGTCTCAAAAAA[-/AAAC]AAACAAAAAAACCCC | 7468 |
rs770491965 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942612 | TCACATTCATCTCAT[A/G]ATAGAAACACGTTCA | 7468 |
rs770497665 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922771 | TCTCTACTAAAAATA[G/T]AGAAATTAGTTGGGC | 7468 |
rs770514753 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951224 | GAGAAGGCAGCATCC[A/G]CTATGTCCGTGCTGG | 7468 |
rs770518775 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972980 | GCCTCAGCCTCCCGA[A/G]TAACTGGGATTACCG | 7468 |
rs770524286 | snp | A/G | 2.70179e-05 | 0.00367535 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955651 | TCTGGGCTGAGCCAT[A/G]GCAGACAGGCTAAGC | 7468 |
rs770543236 | snp | C/G | 3.50336e-05 | 0.00418516 | missense | WHSC1 | GRCh38.p7 | 4:1900673 | GAATTTAGCATCAAG[C/G]AGAGTCCCCTTTCTG | 7468 |
rs770543863 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901591 | CGTCAGGCTACACTC[G/T]TTTCATGGATCTCAT | 7468 |
rs770566682 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947562 | TATTTTAGATGATGA[A/G]TGACTTATTTTAATT | 7468 |
rs770570451 | snp | A/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1920176 | CAAGAGTGGCTGGGC[A/G/T]TGGTGGCTCCCGCCT | 7468 |
rs770589841 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907961 | CACTGTTACCCCCAA[A/C]TACGTCAGAACAAGG | 7468 |
rs770598241 | snp | G/T | 1.68405e-05 | 0.00290172 | missense | WHSC1 | GRCh38.p7 | 4:1918156 | CTATTGAAACCAATT[G/T]CAGGGAAATTGAGGG | 7468 |
rs770598330 | snp | C/G/T | 9.22805e-05 | 0.00679211 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900607 | TTTTCTTTCTTTTTT[C/G/T]TTTTTTTTAATACCA | 7468 |
rs770647758 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930001 | GATTCCTGGTAGGCA[G/T]GTTGGGGTGGGGCCC | 7468 |
rs770661384 | snp | A/G | 4.94556e-05 | 0.00497246 | missense | WHSC1 | GRCh38.p7 | 4:1975294 | CTCCTCTTCTCCCAG[A/G]GACGGAGCTGACTTT | 7468 |
rs770707528 | snp | G/T | 1.7364e-05 | 0.00294647 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953532 | GTCAAAAGGTACAGG[G/T]GCACCTGCGCAGCCT | 7468 |
rs770712941 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971995 | AGGCAGGACGCTCAC[A/G]CCGCTCCTGTACCCC | 7468 |
rs770736637 | snp | A/G | 5.13483e-05 | 0.00506671 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904169 | CTTCTGGATACACAG[A/G]TAGTGATTGGATGTG | 7468 |
rs770794503 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959412 | GGCAGTGGTGGGTGT[G/T]CAAGGGTATTCGGAA | 7468 |
rs770796638 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941952 | GGCCCGATTCTGATA[C/T]GAGTTAGGTGACCAT | 7468 |
rs770823768 | snp | C/G | 3.30781e-05 | 0.00406669 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978774 | CCCGGACGGGCGGTC[C/G]TACTGCTGTGAGCAT | 7468 |
rs770828981 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923012 | GAGCATGTGGACATG[A/G]ATGGGAAAGCGCTGC | 7468 |
rs770832200 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1904267 | AGAGACAAAGACCAC[C/T]TGTTGAAATACAACG | 7468 |
rs770837199 | in-del | -/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893658 | CCAGGCTCAACTGAT[-/C]CTCCTGCCACAGCCT | 7468 |
rs770839409 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896761 | CTTTCTTTCTTTCCT[G/T]CTTTCTTCTCTTTTT | 7468 |
rs770938820 | snp | A/C | 3.295e-05 | 0.00405881 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939742 | TCTTGGGTTTAGCAA[A/C]AGTTCATCTCCTTCT | 7468 |
rs770943961 | in-del | -/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950478 | AAATAGGCAATGGGA[-/G]GAAGAAGAGAAACCG | 7468 |
rs770959685 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946234 | TTCTTAACTTCTAAA[A/G]TTTGGGGGGTCTTGC | 7468 |
rs770966499 | snp | A/G | 1.651e-05 | 0.0028731 | missense | WHSC1 | GRCh38.p7 | 4:1918348 | GCAGAATCCTCAGGA[A/G]TCAGTGAAGAAGCTG | 7468 |
rs770981322 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910935 | TGTCGTTGTGACTTT[G/T]CTCCTGTGCTCCATT | 7468 |
rs770989040 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906250 | TTACTTTTAATTTCT[C/T]TTTTTGGGGATGGAG | 7468 |
rs771003457 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894588 | GAGGTGGGAGGATTG[C/T]TTGGGCCCAGGAGTT | 7468 |
rs771012684 | snp | C/T | 1.65258e-05 | 0.00287448 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942321 | AATTCTTATTTTTTT[C/T]GCCTTCACTGGTAAC | 7468 |
rs771027381 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957093 | TCCTGTAGAGCCAGA[A/G]ACCTTTGTGGCTGAC | 7468 |
rs771028690 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955480 | GTTAATAGTATATCA[C/T]AGTAGCTCTAAATTA | 7468 |
rs771049480 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881606 | TTTGCCATGTTGCCC[A/G]GGCTGGTCTTGAATT | 7468 |
rs771067048 | snp | G/T | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952418 | CAGTAGCTGCAGGGT[G/T]TGCTCTGATTTCAGT | 7468 |
rs771094496 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975411 | CAAAGGTAAGGCTGT[A/G]GCGCCCTCCTTCCCC | 7468 |
rs771094747 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943108 | TATAGAGCATCAGCC[C/T]TCATGTTTCATTGTC | 7468 |
rs771095660 | in-del | -/GGTTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906851 | TTTTAGTAGAGATGG[-/GGTTT]GGTTTCACCATATTG | 7468 |
rs771145606 | snp | A/G | 6.64242e-05 | 0.00576261 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955992 | TAATAGATGGTGGCC[A/G]GCAGAAGTTTGCCAT | 7468 |
rs771158425 | snp | C/G | 1.72187e-05 | 0.00293412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955114 | CTCTTTTCACTATGA[C/G]TGGAGTCAGTGTTTG | 7468 |
rs771176370 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970423 | AGGAACATGTCCTTC[C/T]TGAGTCAGCTGCTGA | 7468 |
rs771177376 | in-del | -/GG | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979683 | CTTCTGAACTCGCTA[-/GG]TTCTTATCAACATTT | 7468 |
rs771183337 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905054 | AGAATCGCTAGAACC[C/T]GGGAGGTGGAGGTTG | 7468 |
rs771198549 | snp | A/G | 1.73856e-05 | 0.0029483 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974726 | GGGGTGTCCTGTCTC[A/G]GTGGACACAGGACAC | 7468 |
rs771211449 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874152 | GTGTTTGGTTTTGCC[G/T]TTTTGTTTTTGTTTT | 7468 |
rs771246546 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950571 | ATACTTCTGAAAGGA[C/T]GCATGGTCTCCACCC | 7468 |
rs771248732 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964910 | CCATCTTGGGTTGAT[C/T]CTCTGCACAGAAACA | 7468 |
rs771249310 | snp | C/G | 0.0126731 | 0.0785871 | missense | WHSC1 | GRCh38.p7 | 4:1956141 | TGGAGGGGGACCGGG[C/G]CAGCCGCTACCAGGG | 7468 |
rs771265108 | snp | A/G | 1.64819e-05 | 0.00287066 | missense | WHSC1 | GRCh38.p7 | 4:1900973 | TCCCAGGAAATGAAA[A/G]GGATTGGGACACCCC | 7468 |
rs771270110 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913884 | CGAGGAGAAAAACCC[A/G]CAGGCCCTGTAGGGC | 7468 |
rs771283245 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924748 | GACTCTCATCTCTAC[-/A]AAAAAAAAAAACAAA | 7468 |
rs771287635 | snp | G/T | 1.64909e-05 | 0.00287144 | missense | WHSC1 | GRCh38.p7 | 4:1900895 | GCCGACAAGCTGAAA[G/T]ATCTTACTTCCCGGG | 7468 |
rs771296047 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882846 | AGACCTACTGCATCA[C/T]GAACTCTGGAGTGGG | 7468 |
rs771300751 | in-del | -/A | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981216 | TTTCCAAAAACTGTT[-/A]AAACTAATGAGCAAG | 7468 |
rs771318960 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879121 | AAGAGAAAGCCCTAG[A/T]TCTTGAGCATGGCAT | 7468 |
rs771341185 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976034 | CCCTGAGCCGGTGTC[C/T]GTCCTCAGCCGTGTT | 7468 |
rs771421826 | snp | A/G | 1.6708e-05 | 0.00289028 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952248 | CAAGTTCCCACGGGC[A/G]GGCAGCTCTGCAGCC | 7468 |
rs771445145 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964238 | TAAATCAGACAAATA[C/T]GAACAAACAGCAGCG | 7468 |
rs771445832 | snp | A/C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914438 | TCAAGTGATTCTCCC[A/C/G]CCTCAGCCTCCTGAG | 7468 |
rs771490267 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926151 | CTTTTTGGGCCTGAA[-/T]TTTTTTTTTTTTTTT | 7468 |
rs771508547 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932328 | CCTGTAATCCCAGCT[A/G]CTCGGGAGGCTGAGG | 7468 |
rs771509829 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | WHSC1 | GRCh38.p7 | 4:1935222 | AAGCTGAGGACACAC[C/T]CAGGAAAAGACTCAG | 7468 |
rs771516421 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923885 | AAGGGTATGCAGATT[C/T]TATCACTTGTGTAGT | 7468 |
rs771542688 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926620 | GGACTACTGGTGCAC[A/G]CCACCACACCCAGCT | 7468 |
rs771567647 | snp | C/T | 1.69738e-05 | 0.00291317 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930795 | GCATTATGCTGATGT[C/T]CTCTGCTTGGGTTGA | 7468 |
rs771574118 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892489 | GTTATATAATTCCTA[A/G]GCACTTATTTTAAAA | 7468 |
rs771641509 | snp | C/G | 1.71032e-05 | 0.00292426 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975432 | CTCCTTCCCCCCAGG[C/G]TCTGTGTTGGCATTT | 7468 |
rs771653259 | snp | A/C | 3.36355e-05 | 0.00410081 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935135 | ATTTTCCCCATTCCC[A/C]ATTCCAAGGTAATGT | 7468 |
rs771655218 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961195 | GCAGTGTGCTGGACC[C/T]GGAGCCCTGATGGTC | 7468 |
rs771683249 | in-del | -/TCCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896708 | ACTCTTCCATTCCTC[-/TCCT]TCCTTCCTTCCTTTC | 7468 |
rs771696699 | snp | A/G | 0.000497389 | 0.0157622 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953125 | GCTGGAGCTCAGATC[A/G]CAGCAAGGTAATCCT | 7468 |
rs771707407 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877823 | ACCCTCCTTCAGGTC[G/T]TTGTGCTTCTCCCTC | 7468 |
rs771717578 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969168 | CAGTGGGAAAAGAAG[A/G]CATGGGGAGCTCCTG | 7468 |
rs771782081 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922886 | AGCTGGGATTGTGCC[A/G]TTGTACTCCAGCCTG | 7468 |
rs771786838 | snp | C/T | 3.32154e-05 | 0.00407512 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918458 | GACCCTGGAGAGTCA[C/T]CCCGACATAGGGAAG | 7468 |
rs771794109 | in-del | -/CTC | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892034 | CTATTTTCTGCCTCT[-/CTC]CTCTAGAATATTAGC | 7468 |
rs771815359 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927427 | AAACTCTAAAAAGAT[-/G]TTGGGGGGAGCACAG | 7468 |
rs771832947 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881228 | GACACAGGCGTGTGC[C/T]ACTACACCTGGCTAA | 7468 |
rs771835213 | snp | C/G | 3.36372e-05 | 0.00410091 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916841 | CCAGATTCTAACTTT[C/G]ATTCTCTAACATTTT | 7468 |
rs771849353 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973118 | CCAAAGTACTGGGAT[A/T]ATAGGTGTGAGCCAC | 7468 |
rs771867435 | snp | A/G | 3.29582e-05 | 0.00405931 | missense | WHSC1 | GRCh38.p7 | 4:1959720 | GGGTGGGGCCTGGTC[A/G]CCAAGAGGGACATCA | 7468 |
rs771940413 | snp | C/T | 1.65732e-05 | 0.00287859 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959757 | TATGTGTCGTTATCC[C/T]CTCCCCTGCTTTTGA | 7468 |
rs771978108 | snp | A/C/G | 3.40085e-05 | 0.00412351 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955139 | TGTTTGGGGTCCTTA[A/C/G]GGTGTGTTTCTTTGC | 7468 |
rs772004750 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887543 | TACAGTGGCACGATC[A/G]TAGCTCACTGTAGCC | 7468 |
rs772005142 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978485 | GAGCCCGCCCGGGCT[A/G]TGGTAGACAGTTTGT | 7468 |
rs772010562 | in-del | -/GGGCTCAAGCTGTCCTCTC | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953885 | CATCCTTGACCTCCT[-/GGGCTCAAGCTGTCCTCTC]GGGCTCAAGCTGTCC | 7468 |
rs772015827 | snp | A/G | 4.94645e-05 | 0.00497291 | missense | WHSC1 | GRCh38.p7 | 4:1900920 | CCCGGGTGTTTAATG[A/G]AGAACCCGGCGCACA | 7468 |
rs772062916 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929532 | CCAAAGGGCTGGTGA[A/G]CAGTGAGGGCTCTGT | 7468 |
rs772067921 | snp | A/G | 3.29739e-05 | 0.00406028 | intron-variant, utr-variant-3-prime, synonymous-codon | WHSC1 | GRCh38.p7 | 4:1942350 | ACAGCTTTTGTGGGA[A/G]CCCACACCAGTCAAG | 7468 |
rs772097907 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897916 | GCAGGCATGAGCCAC[C/G]TCACCCAGCTGCTGA | 7468 |
rs772120465 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927824 | AGAGTCTCCAATTAC[A/G]TTGGCAATGTTTTAG | 7468 |
rs772127940 | snp | A/G | 3.38937e-05 | 0.00411652 | missense | WHSC1 | GRCh38.p7 | 4:1956183 | TCGGAAGAGTCTTCA[A/G]AAACGGTACGGAGAT | 7468 |
rs772129697 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974970 | GAATGGGGACACTCG[C/T]GTGGGCCTGTTTGCC | 7468 |
rs772131547 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906161 | TATGATGCCATGTTT[-/A]GCTGTTAGCCTCTCA | 7468 |
rs772133945 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895784 | TAGACCTGTTTTGAC[A/G]TTTTTTGGTCTCCGG | 7468 |
rs772134030 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882919 | ATGCCCTTGAGTTGA[C/G]AGCTACTGTCTGAAT | 7468 |
rs772150093 | in-del | -/AT | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980056 | GTCTCTGCTGATCAC[-/AT]GTGCCCTCTGCCAGG | 7468 |
rs772152015 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884164 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 7468 |
rs772192753 | snp | C/G | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1948943 | GATAGCGCTGGGGCT[C/G]TCTCCCCTGAGCCAT | 7468 |
rs772239231 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964248 | AAATACGAACAAACA[A/G]CAGCGGAGGTTAAAA | 7468 |
rs772239992 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | WHSC1 | GRCh38.p7 | 4:1957959 | GCTGAAGCTCGTTTT[C/T]GTGAAATTAAGCTTC | 7468 |
rs772250372 | snp | A/G | 1.67055e-05 | 0.00289006 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958083 | GAGGGAGTCTTCCCC[A/G]AGGGCCGTGAGAGGT | 7468 |
rs772255268 | snp | A/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979538 | ATGGTGTTGTAAGAT[A/T]TCCTCCCGTAGTTTT | 7468 |
rs772271850 | snp | C/T | 0.000117146 | 0.0076524 | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952255 | CCACGGGCGGGCAGC[C/T]CTGCAGCCTGGCCGG | 7468 |
rs772299034 | snp | G/T | 1.67995e-05 | 0.00289819 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951024 | AGGGCATGGCCACCC[G/T]CTGTGTTCTGCGACT | 7468 |
rs772303052 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914074 | GTCGCCCAGGCTAGA[A/G]TTCAGTGGCGGGATC | 7468 |
rs772320095 | snp | C/T | 0.000157245 | 0.00886554 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938427 | CTTTCTTTTTTTTTT[C/T]TTTTTTTTTTTTTTA | 7468 |
rs772328044 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894748 | TCCAACTAGAACTGC[A/G]TTGGAATGTAAGCTC | 7468 |
rs772357732 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976397 | CTGAAGTTCCTGGAG[C/T]GTAGCTCGCTCTTCT | 7468 |
rs772383642 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907357 | TAACCCTGCAGCCAC[C/T]TAGTGTTTGGTTAAT | 7468 |
rs772384561 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936420 | TCACACCTGTAATCC[C/G]AGCACTTTGGGAGGC | 7468 |
rs772385965 | snp | A/G | 3.53951e-05 | 0.0042067 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978595 | AATGTTGAAGTCGTG[A/G]TTCCATCACTTCTGT | 7468 |
rs772392283 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944792 | AGATGGATCTTTGGG[C/G]CTTTCCTCAGTGTTC | 7468 |
rs772413927 | in-del | -/ATA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925773 | TATCTATATATATAT[-/ATA]TTTTTTTTGTTTGTT | 7468 |
rs772434102 | in-del | -/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938417 | TTTTTTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 7468 |
rs772437510 | snp | C/T | 8.73115e-05 | 0.00660667 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953242 | TCTGAAGAGGAGTTG[C/T]TTGATTTTAGTGGCT | 7468 |
rs772448843 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965171 | TGATAGATCTACTAG[A/G]CAGAGACTCTAAAAC | 7468 |
rs772469224 | snp | A/C | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952274 | CAGCCTGGCCGGCCA[A/C]CTGCTCCTGCAACCC | 7468 |
rs772470252 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964626 | GCAGACAAAGAGGTG[C/T]GCTGCGCTGCCGTTG | 7468 |
rs772470710 | snp | A/G | 1.64852e-05 | 0.00287094 | missense | WHSC1 | GRCh38.p7 | 4:1961074 | GGGGAGCTGATCGAC[A/G]AGGAGGAGTGCATGG | 7468 |
rs772473493 | snp | G/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869833 | CATTTTGAATTAATT[G/T]TTGTTAAGGGTGTAA | 7468 |
rs772482187 | in-del | -/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907614 | CTACCTGTTGAATCT[-/C]CTTTTTTTTTTTTTT | 7468 |
rs772494131 | in-del | -/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944090 | ATCTCAGCGGGGGGT[-/G]GGGGTGACATCGTTC | 7468 |
rs772548797 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874264 | TTTGCTTGATTGTAG[-/T]TAAGTGTGACCTTGT | 7468 |
rs772566981 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878044 | AAGAAAAATAAAATT[A/T]AAAAAAAGTATTATA | 7468 |
rs772571701 | snp | A/G | 1.65252e-05 | 0.00287443 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938516 | GGAGGCAGCCTCCTC[A/G]CTCAAGAGCCAGGCA | 7468 |
rs772587139 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896972 | GCCCAGGAGTTGGAG[A/C]CCAGCCTCGGCAACA | 7468 |
rs772643266 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966759 | TTTTGTTTTCTATAT[A/G]ATTTAAGCTACTCAT | 7468 |
rs772654247 | snp | C/T | 0.000216351 | 0.0103985 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955306 | GCGACACCACGCCCA[C/T]GTCAACGTGAGCTGG | 7468 |
rs772656534 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971946 | TGCCAGCTGATGCTC[A/C]GTGAGCCAGACACTT | 7468 |
rs772679711 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907858 | CCTTGTGATCCACCC[A/G]CCTTGGCCTCCCAAT | 7468 |
rs772700430 | in-del | -/G | 4.95864e-05 | 0.00497903 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935276 | GGTAATTGTGTTCCA[-/G]GGTTTGCTTGACCTG | 7468 |
rs772745678 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970826 | GGTCACATAAAGGGC[C/T]GCCAACAGGACAGGA | 7468 |
rs772747061 | snp | A/G | | | missense | WHSC1 | GRCh38.p7 | 4:1900821 | CCCAGCTCTCCAGTA[A/G]CCTGCAGGAGGGGGT | 7468 |
rs772749277 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915434 | TTTATTTTCATAGTT[C/G]TATTTTAGAATTTCA | 7468 |
rs772800984 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968096 | AAATAACCCTAGACC[A/T]TGCATTCTAGTGCTC | 7468 |
rs772810274 | snp | C/G | 2.7702e-05 | 0.00372159 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978876 | GAAGAGGCGGCGGCG[C/G]AGGGGCTGGCGGAGA | 7468 |
rs772817636 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899338 | CATAGCCCTGTTGCG[C/T]GGGCATCCTGTGCGT | 7468 |
rs772852137 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932677 | CTTGAACCTGGGAGG[C/T]GGAGATTGCAGTGAG | 7468 |
rs772862979 | in-del | -/GAG | 1.64808e-05 | 0.00287057 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951206 | GTATGTGTGCCAGGT[-/GAG]GAGAAGGCAGCATCC | 7468 |
rs772879787 | in-del | -/TGACC | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980584 | TACTCCGTGGTTTTG[-/TGACC]TGTAAGCGTGGGGTT | 7468 |
rs772887051 | snp | A/T | 2.31361e-05 | 0.0034011 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955386 | GCCTCTCACACTCCC[A/T]GGAGCCACATATCAA | 7468 |
rs772894930 | snp | A/G | 1.73655e-05 | 0.0029466 | missense | WHSC1 | GRCh38.p7 | 4:1918618 | TGTCAAAAACACAGG[A/G]ATGAGGTCAGTACTA | 7468 |
rs772944380 | snp | A/C/T | 1.79897e-05 | 0.00299908 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930598 | TTACGGATTTAACTT[A/C/T]TCATTGCACCTTCTC | 7468 |
rs772950890 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935080 | CTGGGTAGGTTCTCA[A/C]AGTGCTTCAAATGCA | 7468 |
rs772951098 | snp | A/G | 1.66205e-05 | 0.00288271 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951055 | AGTGAACTGTCATCC[A/G]CCTCCTTCATCTCTA | 7468 |
rs772958412 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958340 | AGCCTCCCACCTGCA[A/C]CAGGCTGTTGCCAAG | 7468 |
rs772960069 | snp | A/C | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979470 | TGAATTGTTCCTCAG[A/C]AACGCTTCTTTTCCA | 7468 |
rs772984703 | snp | A/G | 1.65051e-05 | 0.00287267 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975007 | GACATTCCTGCAGGT[A/G]CAAGCTCTGGGGACC | 7468 |
rs773005750 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876093 | GGTTGCAGTGCCTGT[A/G]GTCCCAGCTACTCGG | 7468 |
rs773033982 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894910 | TTTCATCTTCTCAAA[C/T]TGAAACTCTGTCCCA | 7468 |
rs773035225 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945929 | TTCTCTAACATCTAG[C/G]CCTTTTAAATTTTTA | 7468 |
rs773042514 | snp | C/T | 2.27436e-05 | 0.00337213 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953228 | GCAGCATGGCTGCCT[C/T]TGAAGAGGAGTTGCT | 7468 |
rs773049879 | snp | A/G | 0.000156287 | 0.00883849 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978931 | GCGGCCGCTTGGCCG[A/G]ATCCAGGGGCGGTGC | 7468 |
rs773076474 | snp | C/T | 3.30175e-05 | 0.00406296 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975267 | GGCAGGTGTTTCCAA[C/T]TTGGTGTCTGTCTCC | 7468 |
rs773117985 | snp | A/G | 3.30633e-05 | 0.00406578 | missense | WHSC1 | GRCh38.p7 | 4:1978770 | GCACCCCGGACGGGC[A/G]GTCCTACTGCTGTGA | 7468 |
rs773158001 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945079 | TGTCCCACTGCTGCT[G/T]CTTGAGTGGGTGGAG | 7468 |
rs773161352 | snp | A/G | 1.86138e-05 | 0.00305067 | intron-variant | WHSC1 | GRCh38.p7 | 4:1901299 | GACCTTGAGCAGTGA[A/G]CATGGCCACCCTATG | 7468 |
rs773193018 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879826 | GGCCCATGGCACTTG[-/TG]TGTGTGTGTGTGTGT | 7468 |
rs773226638 | snp | A/G | 1.7621e-05 | 0.0029682 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959435 | ATTCGGAAGGCTCTC[A/G]TGTGTGGACCAAGAC | 7468 |
rs773229335 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904852 | TTAAGAATGTACGGC[C/T]GGGCACGGTGGCTCA | 7468 |
rs773244806 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968854 | GGAAAGATCCTAAAG[G/T]TAGTGTTCAAAGAAA | 7468 |
rs773246822 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976792 | GGTGCAGGCACATCA[A/G]GCGCTCATGCAGCGA | 7468 |
rs773255189 | snp | A/G | 3.31279e-05 | 0.00406975 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900726 | AAAGATGAAGCAGGC[A/G]CCAGAAATCCTCGGC | 7468 |
rs773264563 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953668 | GACATCGGCTGGGTT[C/G]GGTTTTCTTTGACAA | 7468 |
rs773277218 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921714 | TTGAACCTGGGAGAC[A/G]GAGGTTGCAGCGAGC | 7468 |
rs773277562 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906535 | ATGAGCCACAGTGCC[G/T]CAGCCCAACTTATAT | 7468 |
rs773294676 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974034 | CCTTATCAGGTTGCT[G/T]CCTCGAAAGCCTTCC | 7468 |
rs773295682 | snp | A/G | 3.43124e-05 | 0.00414186 | missense | WHSC1 | GRCh38.p7 | 4:1901198 | TCCTTGCTGGAGCAG[A/G]GCCTTGTCGAAGCAG | 7468 |
rs773295766 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907917 | AGCCTCCATCTCTTT[C/T]GTTGCATGATGGCTG | 7468 |
rs773342195 | snp | C/T | 1.66316e-05 | 0.00288367 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938574 | TTGGCTTCTGGGTGC[C/T]CAGGCTGGGCTGGGT | 7468 |
rs773355536 | snp | A/G | 1.85228e-05 | 0.0030432 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974642 | TCCTCCCCGGCGCTC[A/G]CTAAGGCTCGGTCCT | 7468 |
rs773370922 | snp | A/C | 1.65157e-05 | 0.0028736 | missense | WHSC1 | GRCh38.p7 | 4:1918334 | CTTTGGGAGAAATGG[A/C]AGAATCCTCAGGAGT | 7468 |
rs773398525 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912328 | TCTATTTCTTTCCCC[C/T]CATTCTCCCCATATA | 7468 |
rs773417934 | snp | C/G | | | missense | WHSC1 | GRCh38.p7 | 4:1916944 | AGCTTGGATATTTGA[C/G]AAGAGCCTCGTAGCT | 7468 |
rs773424310 | in-del | -/TGT | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973924 | GCTGCTGGGTGGAGA[-/TGT]TGTCTCCAGTTCCTG | 7468 |
rs773445820 | in-del | -/TTG | 1.69515e-05 | 0.00291126 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974772 | AACAAGGAACACAAC[-/TTG]TTCAATGTGCTTTAT | 7468 |
rs773478602 | snp | C/T | 1.74427e-05 | 0.00295314 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974720 | GGTTTGGGGGTGTCC[C/T]GTCTCAGTGGACACA | 7468 |
rs773487528 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1978337 | AGCACAGCAGCCCCT[G/T]CCTGTCCACGCCGCG | 7468 |
rs773506215 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953723 | TTCCATCCTAAATAT[C/G]ACCCTAAAGATGCTT | 7468 |
rs773513882 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898219 | AGCCTCCTGAGTAGC[A/G]GGGACTACAGGTGCA | 7468 |
rs773520954 | snp | A/G | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949282 | AGAGCCTTAAAGTGT[A/G]CACTGCTCTGATTAG | 7468 |
rs773530545 | in-del | -/AAATA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964953 | CAAAACAAGAACAAT[-/AAATA]AAAATAACAAAAACA | 7468 |
rs773544606 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962968 | CACATTCCTCTCAGG[A/G]CCCTGTCAACACAGG | 7468 |
rs773563373 | snp | G/T | 1.65296e-05 | 0.00287481 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955838 | CATTTGGGTGAAACT[G/T]GGGAACTACAGGTGT | 7468 |
rs773602761 | in-del | -/CTTG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910611 | TAGGAATTAACCCTC[-/CTTG]CTTTATATAGGAAAA | 7468 |
rs773634505 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964067 | ATAGAAGGTGACCCT[C/T]GTGAGCAGACCTTCC | 7468 |
rs773651423 | snp | A/G | 1.69939e-05 | 0.00291491 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952057 | CCCTTGTGGTAAGAG[A/G]TGCAGAAGGGACTGC | 7468 |
rs773651550 | snp | A/G | 1.66299e-05 | 0.00288352 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955954 | GTCTCTGAGGAGTCT[A/G]TGAATCCTGTTTTTA | 7468 |
rs773660936 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | WHSC1 | GRCh38.p7 | 4:1900820 | GCCCAGCTCTCCAGT[A/G]GCCTGCAGGAGGGGG | 7468 |
rs773671393 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961533 | TGGGTAAGGTCTCAG[C/T]ATCTTCTCTGTTGTG | 7468 |
rs773691968 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | WHSC1 | GRCh38.p7 | 4:1959682 | AGTACCCAGAGACCA[A/G]GATCATCAAGACAGA | 7468 |
rs773694055 | snp | A/G | 3.74981e-05 | 0.00432986 | missense | WHSC1 | GRCh38.p7 | 4:1976554 | GAGCAAAAGGGGAAG[A/G]GAAGAGGCAGTCAGA | 7468 |
rs773696835 | snp | G/T | 1.65203e-05 | 0.002874 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975016 | GCAGGTACAAGCTCT[G/T]GGGACCCTGCATGGG | 7468 |
rs773702827 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878546 | GCAGGGACTTTTTTC[C/T]TTTTGCTTGGCTTGC | 7468 |
rs773711025 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927752 | AAAAAAAAAAAAAGC[C/G]GTGTAGGGAGCAGGC | 7468 |
rs773737659 | snp | C/T | 0.000402495 | 0.0141805 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978955 | GCGGTGCAGGGCGGC[C/T]GGCCCTGCCTGCGGG | 7468 |
rs773740488 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893462 | TGGGCGACAGAGACT[C/T]CGTTTCAATAAAAAA | 7468 |
rs773746799 | snp | A/C | 2.65919e-05 | 0.00364626 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976444 | CCTGTGTAATTCTTT[A/C]CGGTGATCTGTGCTT | 7468 |
rs773777990 | in-del | -/AAAA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875603 | TTTGGTTTGCTAGTT[-/AAAA]AATCCAGACAGATTG | 7468 |
rs773785747 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877697 | TCTGTTCCAGCCACA[C/T]GGGCCTCTTGCCTGC | 7468 |
rs773803330 | snp | C/T | | | missense | WHSC1 | GRCh38.p7 | 4:1959543 | AAGTGCAACTGCAAG[C/T]CCACAGATGAGAATC | 7468 |
rs773803795 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929687 | TGTCATGAAATATTA[-/T]GATGTTTTTCAGACA | 7468 |
rs773811007 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908303 | TACTAAAGATCTGTG[C/T]ACAGAAGAAGGGAGT | 7468 |
rs773829165 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880492 | TATCAGTTGTGTGCC[A/G]ATGATGAGCCAAGAC | 7468 |
rs773890550 | snp | C/T | 3.32049e-05 | 0.00407448 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952121 | AGCTGTGTGAGAAGC[C/T]GGGCAGCCTCCTGCT | 7468 |
rs773903305 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953175 | TGGAGAATGCTTGGA[-/GT]CTAGTGAGCAAGGTT | 7468 |
rs773908730 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951113 | CTCGGAGTCCCCATA[C/T]GAAAGTGCAGACGAA | 7468 |
rs773934948 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936265 | CGTGAGCCCTTTTCC[C/T]AGTGTATGAAGTGGT | 7468 |
rs773963152 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907964 | TGTTACCCCCAAATA[C/T]GTCAGAACAAGGACA | 7468 |
rs773971638 | snp | C/T | 1.68584e-05 | 0.00290326 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930781 | CTCTGGTAAACATAG[C/T]ATTATGCTGATGTCC | 7468 |
rs773978600 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973028 | TGGATAATTTTTTGT[A/G]TTTTTATTAGAGACA | 7468 |
rs773979451 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945202 | AGATTTAAAATGGGG[C/T]GCTCAGGGACTGGGG | 7468 |
rs773985036 | snp | C/T | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982616 | GTGGGCCAGGGTGTC[C/T]TAGGAAGCCCCCAGC | 7468 |
rs773996098 | snp | A/C | 3.53701e-05 | 0.00420521 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930606 | TTAACTTCTCATTGC[A/C]CCTTCTCCCGTTCCC | 7468 |
rs774002274 | in-del | -/TTTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1925773 | ATATCTATATATATA[-/TTTT]TTTTTGTTTGTTTGT | 7468 |
rs774022532 | snp | A/G | 0.000329707 | 0.0128353 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951227 | AAGGCAGCATCCGCT[A/G]TGTCCGTGCTGGTGT | 7468 |
rs774037899 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1876344 | GGTTTCAACAAAATA[C/T]ACAAGGATAGAAATT | 7468 |
rs774083111 | snp | G/T | 0.000119712 | 0.00773575 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904172 | CTGGATACACAGGTA[G/T]TGATTGGATGTGTTA | 7468 |
rs774107912 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977106 | TACAGTGGGAATGGA[A/G]GGGCCCAGAGCCCCT | 7468 |
rs774111361 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891492 | AATTATCAGAGTGGG[C/T]TTTAGCTGACATCTA | 7468 |
rs774143460 | snp | C/T | 0.000242189 | 0.0110016 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959457 | GACCAAGACAGCTTA[C/T]TCCTTCCCTGCAGGT | 7468 |
rs774150914 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909186 | CCTTTGACATGTCCC[C/T]GTCAGCCCTTGAGCA | 7468 |
rs774166527 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977894 | ACTTCTGAGAGGCCA[A/G]GGTGGATGGATCACT | 7468 |
rs774194052 | in-del | -/T | 9.88745e-05 | 0.00703047 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974827 | ATAACATGCGATTGC[-/T]TAACACTTGACCGAA | 7468 |
rs774234132 | snp | A/G | 3.29571e-05 | 0.00405924 | missense | WHSC1 | GRCh38.p7 | 4:1959627 | CCGCAGGTGTGTCCC[A/G]CGGGCGAGTTCTGCC | 7468 |
rs774250392 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885535 | GCCCCTGTTGACATG[C/T]ATTTTGATAGGACCT | 7468 |
rs774259457 | snp | C/T | 1.79457e-05 | 0.00299542 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974663 | GCTCGGTCCTCTCCA[C/T]GTGGTCCTGACCTGT | 7468 |
rs774260711 | in-del | -/TTAT | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946259 | TCTTGCATTTATTTA[-/TTAT]TTATTTATTTATTTA | 7468 |
rs774265779 | snp | A/C/G/T | 0.000251241 | 0.0112057 | missense | WHSC1 | GRCh38.p7 | 4:1978833 | CCAAGACTGAGAAGC[A/C/G/T]CCCCCCAGAGCCAGG | 7468 |
rs774270285 | snp | A/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948621 | TATTGTAAGGTCTAT[A/G]TTCTGTATGTGGGTC | 7468 |
rs774302845 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932164 | ACAGATGTCTGGGCA[C/T]GGTGGCTCACACCTG | 7468 |
rs774304520 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930324 | TAGAGGCTGGGTCTT[A/G]AGTGAGTTAGTGGTT | 7468 |
rs774320917 | snp | C/T | 1.65441e-05 | 0.00287607 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978777 | GGACGGGCGGTCCTA[C/T]TGCTGTGAGCATGAC | 7468 |
rs774325375 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939750 | TTAGCAAAAGTTCAT[C/G]TCCTTCTGCATCCTT | 7468 |
rs774362280 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896644 | GTGCTAGGATTACAA[G/T]TAGTGAACCACTGTG | 7468 |
rs774369274 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956865 | GCAGGCGGGGACCCG[C/T]GTATTTAAAGCTTGG | 7468 |
rs774378704 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947797 | GTTCAAGGTCTGTAA[C/T]TGTATTTCAAAAACG | 7468 |
rs774410104 | snp | C/T | 1.65693e-05 | 0.00287826 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952133 | AGCCGGGCAGCCTCC[C/T]GCTCTGTGAAGGACC | 7468 |
rs774415530 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980179 | GGTATGACACCCACT[C/G]TCCTGTGAGATTTCA | 7468 |
rs774429583 | in-del | -/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893543 | TTTTTTTGTTTTTTG[-/G]TTTTTTTTTTTTTTT | 7468 |
rs774459377 | snp | C/T | 3.31532e-05 | 0.0040713 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956022 | TCCCAAAAATGTTCC[C/T]CCAAATATTCAGAAA | 7468 |
rs774461679 | in-del | -/CCC | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973385 | TGTCCCATGTGCATG[-/CCC]CGTGCTGTCCTCGTC | 7468 |
rs774475647 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963289 | TTGTGTTTTAACCCT[C/T]ATGTGGGGACCAGTG | 7468 |
rs774534172 | snp | A/G | 1.64936e-05 | 0.00287168 | missense | WHSC1 | GRCh38.p7 | 4:1900751 | CTCGGCAGTGCCAAC[A/G]GGAAGACTCCGAGCT | 7468 |
rs774539765 | in-del | -/TTC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887321 | ATCACTTTTGACATG[-/TTC]TTCTTTTTTTTTAAA | 7468 |
rs774556109 | snp | G/T | 1.651e-05 | 0.0028731 | missense | WHSC1 | GRCh38.p7 | 4:1918353 | ATCCTCAGGAGTCAG[G/T]GAAGAAGCTGCTGAA | 7468 |
rs774605113 | snp | C/T | 1.67379e-05 | 0.00289287 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1956145 | GGGGGACCGGGGCAG[C/T]CGCTACCAGGGGGTC | 7468 |
rs774614242 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926702 | TCTCAAACACCTGAC[C/T]TCAGGTGATCTGCCC | 7468 |
rs774625684 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966648 | GGTGACAGAGCAAGA[-/CT]CTGTCTCAAAAAAAA | 7468 |
rs774737951 | snp | A/G | 2.01656e-05 | 0.00317528 | missense | WHSC1 | GRCh38.p7 | 4:1976574 | AGGCAGTCAGAGGAC[A/G]AGTGCTTCCGCTGCG | 7468 |
rs774762006 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951984 | CCATGCATGTTATTA[C/T]ATATCCTTGAGTAGC | 7468 |
rs774795000 | in-del | -/GAC | 1.64757e-05 | 0.00287012 | cds-indel | WHSC1 | GRCh38.p7 | 4:1935214 | GATGCTGAAGCTGAG[-/GAC]GACACACCCAGGAAA | 7468 |
rs774823652 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873753 | AAGTAGCTGGAATTA[A/G]GCTTACTAAGCTACA | 7468 |
rs774840645 | snp | A/G | 5.02138e-05 | 0.00501043 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961162 | ACAAGGTAATGCGGA[A/G]CTCCACTGTGAGCTT | 7468 |
rs774847026 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907071 | TGAGGCTGGGACTCA[A/G]GAATCAGCCTGCCAG | 7468 |
rs774856596 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964239 | AAATCAGACAAATAC[A/G]AACAAACAGCAGCGG | 7468 |
rs774859256 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980325 | CACCCTGAGAAGGGG[A/G]CACCATGTGTGCCTT | 7468 |
rs774862220 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880573 | GGAGGGACAGTGAGC[-/A]AAGGTCATATCTTTG | 7468 |
rs774888825 | snp | A/G | 1.66782e-05 | 0.0028877 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959782 | TTTTGAGAAATTACG[A/G]TTCACTGGGTAATTA | 7468 |
rs774901153 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882902 | TCCTTCATGTGATTC[C/T]GATGCCCTTGAGTTG | 7468 |
rs774922532 | snp | C/T | 1.69887e-05 | 0.00291446 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930796 | CATTATGCTGATGTC[C/T]TCTGCTTGGGTTGAT | 7468 |
rs774930051 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899363 | GTGCGTTGCAGGAGA[C/T]GCAGCAGCATCCATG | 7468 |
rs774947636 | snp | C/T | 3.30017e-05 | 0.00406199 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1916899 | TGCACGCCAGTATCA[C/T]GTACAGTTCTTTGGT | 7468 |
rs774986111 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1912875 | CTGCTTTCCCTAGTT[A/G]TTTACATTGTTTTCT | 7468 |
rs774998796 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977988 | AAAAATTAGCTGGTC[A/G]TGGTGGCGGGCGCCT | 7468 |
rs775000654 | snp | A/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946602 | AAGAAATATTCTGAT[A/T]CATATTTTAGGACTT | 7468 |
rs775000732 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919920 | AGCCTGGCGACAGAA[-/T]TGAGACGCCGTCTCA | 7468 |
rs775004507 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913916 | GATCCCTACAGTTCT[A/G]TGCTGTGTTCTTTCT | 7468 |
rs775004764 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | WHSC1 | GRCh38.p7 | 4:1935225 | CTGAGGACACACCCA[A/G]GAAAAGACTCAGGAC | 7468 |
rs775021788 | snp | A/G | 1.71781e-05 | 0.00293066 | intron-variant | WHSC1 | GRCh38.p7 | 4:1975436 | TTCCCCCCAGGCTCT[A/G]TGTTGGCATTTTGCA | 7468 |
rs775054313 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1888901 | CCATGTATATTAGTA[-/T]TTTTTTTTTTTTTTT | 7468 |
rs775113556 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922996 | CCCAGAACAGGCTCT[C/T]GAGCATGTGGACATG | 7468 |
rs775210009 | snp | C/T | 1.67728e-05 | 0.00289588 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935137 | TTTCCCCATTCCCCA[C/T]TCCAAGGTAATGTAA | 7468 |
rs775232795 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931278 | GAGAGCTCATAGGGC[A/G]AGAAGGGTGACTGGA | 7468 |
rs775261360 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897994 | GGAGGACCACTGTTT[C/T]CTCCAAATATTTTTG | 7468 |
rs775275012 | snp | A/C | 3.52796e-05 | 0.00419983 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953543 | CAGGTGCACCTGCGC[A/C]GCCTTGCTGTGGGTT | 7468 |
rs775278127 | snp | C/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879698 | ATCTTTGCATGTGCT[C/G/T]TTGCTTCTTCCTGAG | 7468 |
rs775280267 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957829 | TGGGAACCAGAAACT[A/C]TACTTAACATTGAAA | 7468 |
rs775366810 | snp | C/T | 1.65023e-05 | 0.00287244 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939788 | AATGAGGTAAAATAA[C/T]AATAATAACGATAAC | 7468 |
rs775385175 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873514 | CTTGCTGAAGTGTGC[A/G]GACCCAAATGAAGCA | 7468 |
rs775398974 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964265 | AGCGGAGGTTAAAAT[A/G]GAGTCATTGAGAGGA | 7468 |
rs775406011 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974834 | TGCGATTGCTAACAC[C/T]TGACCGAATATATCA | 7468 |
rs775406978 | snp | C/T | 1.66905e-05 | 0.00288876 | missense | WHSC1 | GRCh38.p7 | 4:1918480 | ATAGGGAAGAGTACT[C/T]CTCAAAAGACGGCAG | 7468 |
rs775420062 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892551 | TCTGTTCCTGTCCCC[C/T]TTAGAAAACCACTGA | 7468 |
rs775424952 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1955481 | TTAATAGTATATCAC[A/G]GTAGCTCTAAATTAA | 7468 |
rs775457476 | snp | A/G | 5.15743e-05 | 0.00507784 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974745 | GACACAGGACACCAC[A/G]GTTTTCAGTACAACA | 7468 |
rs775476451 | snp | A/G | 1.66432e-05 | 0.00288467 | missense | WHSC1 | GRCh38.p7 | 4:1918471 | CACCCCGACATAGGG[A/G]AGAGTACTCCTCAAA | 7468 |
rs775479825 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884291 | TGTAGAGATGGGATT[G/T]TGCCATGTTGCCCAG | 7468 |
rs775489284 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950590 | TGGTCTCCACCCCGG[C/T]GGCAGCTGGACTGCA | 7468 |
rs775515493 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944839 | TCTTTTTTCAGCATA[C/T]TGACTCCAGGTGTAG | 7468 |
rs775527141 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932364 | GAATCTCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 7468 |
rs775530229 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923893 | GCAGATTCTATCACT[C/T]GTGTAGTTTGAAAAG | 7468 |
rs775533504 | snp | A/T | 2.06149e-05 | 0.00321046 | missense | WHSC1 | GRCh38.p7 | 4:1978857 | AGCCAGGGAAGCCGA[A/T]GGGGAAGAGGCGGCG | 7468 |
rs775588159 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884878 | CTTTGGGAGGCCGAG[C/G]CAGGCGGATCACCTG | 7468 |
rs775593120 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | WHSC1 | GRCh38.p7 | 4:1901003 | CCTAACACTACCCCT[A/G]TCAAAAATGGCTCTC | 7468 |
rs775597844 | snp | C/T | 1.64841e-05 | 0.00287085 | intron-variant, utr-variant-3-prime, missense | WHSC1 | GRCh38.p7 | 4:1942355 | TTTTGTGGGAGCCCA[C/T]ACCAGTCAAGTTGGA | 7468 |
rs775616493 | snp | A/G | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870649 | GCCCCTGGACCAGGC[A/G]TCCTCCCCTCGCGAG | 7468 |
rs775641319 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911823 | GGAAAGAACTTCAGA[A/C]TGTTACACTCATTTA | 7468 |
rs775675257 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891567 | GTGTTAAAGCTCCCC[A/G]GAGAACCGGGCACGG | 7468 |
rs775675771 | in-del | -/TGC | 1.65787e-05 | 0.00287907 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935302 | ACCTGTCAGAGTGTA[-/TGC]TCTGTGACTCTTGGT | 7468 |
rs775677747 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976911 | ACGGGGTAGCCCCTG[A/G]AACCTCCAGGAGGGA | 7468 |
rs775690640 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954426 | GAATGCAGTGGTGTG[-/A]ATCATGGCTCACTGT | 7468 |
rs775693123 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965226 | ACTAAAGGAAAACCT[C/G]CAGAAAGTCAAGAAA | 7468 |
rs775707973 | snp | A/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981051 | AACAGCAGAATCGGC[A/T]TTGCAGTGCACTTTG | 7468 |
rs775725843 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926826 | CTAATTTTTACACAT[A/C]CATTAGATTGGAACC | 7468 |
rs775745761 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882930 | TTGAGAGCTACTGTC[A/T]GAATTTCCTGACTGA | 7468 |
rs775748104 | snp | C/T | 3.34426e-05 | 0.00408903 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953214 | GGCCAGGTGCTTTAG[C/T]AGCATGGCTGCCTCT | 7468 |
rs775748189 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894794 | TTTTTGGGGGTATAC[G/T]TAACATAAAATTTAC | 7468 |
rs775766911 | in-del | -/ACAG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917319 | TGTGTATACACACAC[-/ACAG]ACAGAGGGATTAATG | 7468 |
rs775781891 | snp | A/G | 1.69284e-05 | 0.00290928 | missense | WHSC1 | GRCh38.p7 | 4:1918568 | CCATGCCACGAAGCA[A/G]GAAGGGAGATGCAGC | 7468 |
rs775830577 | snp | A/G | 2.65213e-05 | 0.00364142 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955658 | TGAGCCATAGCAGAC[A/G]GGCTAAGCCTGGCCG | 7468 |
rs775845035 | snp | A/C/T | 3.53909e-05 | 0.00420647 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978598 | GTTGAAGTCGTGATT[A/C/T]CATCACTTCTGTGTG | 7468 |
rs775860726 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1961082 | GATCGACGAGGAGGA[A/G]TGCATGGCGAGAATC | 7468 |
rs775867101 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937853 | AGCCCTTGAGAAAAG[C/T]TTCATGATCCCTTCT | 7468 |
rs775874420 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922200 | AGCTGTCATTGTTTG[C/T]AGAAGTCTATGTAGA | 7468 |
rs775885762 | snp | C/T | 1.6884e-05 | 0.00290547 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961181 | CACTGTGAGCTTCTG[C/T]AGTGTGCTGGACCTG | 7468 |
rs775933350 | snp | C/T | 1.67027e-05 | 0.00288982 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978666 | TCCTTGGCATCATTG[C/T]GACGTGTGTGGCAAA | 7468 |
rs775974209 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943035 | TTTGATCCAAGGCCC[C/T]GGACCAAGGGGATAC | 7468 |
rs775997743 | snp | A/C | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952375 | CTCTGGAGCTTGTAG[A/C]CCACAGCTGGCAGGT | 7468 |
rs776016359 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979417 | GTGATCATTACTCTG[C/G]TCTTTGGAAATGGCT | 7468 |
rs776021906 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980401 | AACATTCAGCAGCAG[G/T]TGCTTTTTTATGGCC | 7468 |
rs776037394 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932439 | CAAGAGTCAATCTCC[-/A]AAAAAAAAAAAAAAA | 7468 |
rs776052213 | snp | C/T | 3.32928e-05 | 0.00407987 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959778 | CTGCTTTTGAGAAAT[C/T]ACGGTTCACTGGGTA | 7468 |
rs776067673 | snp | C/G | 1.64963e-05 | 0.00287192 | missense | WHSC1 | GRCh38.p7 | 4:1904351 | GTTTCTGCAGATCCA[C/G]TCCTTCACAGCTATA | 7468 |
rs776074715 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899045 | GTTGGTATGATATGA[G/T]CTGGAAGAGGAACTG | 7468 |
rs776087550 | snp | C/T | 5.11775e-05 | 0.00505827 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955327 | CGTGAGCTGGTGCTT[C/T]GTGTGCTCCAAAGGT | 7468 |
rs776092631 | snp | A/G | 1.68286e-05 | 0.0029007 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918158 | ATTGAAACCAATTTC[A/G]GGGAAATTGAGGGCC | 7468 |
rs776092744 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972982 | CTCAGCCTCCCGAGT[A/G]ACTGGGATTACCGGT | 7468 |
rs776114283 | snp | A/G | 9.9595e-05 | 0.00705603 | missense | WHSC1 | GRCh38.p7 | 4:1955301 | GGGAAGCGACACCAC[A/G]CCCACGTCAACGTGA | 7468 |
rs776127861 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969933 | ATTATTTTCTAAGCA[A/G]AGCCTAAACCTCAAG | 7468 |
rs776133352 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915509 | GTTTCTCTGTTGGGT[A/G]TCTTCTCTTCCCTTG | 7468 |
rs776145744 | snp | A/G | 1.66189e-05 | 0.00288256 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1917019 | CAAGCAGGCACCCAC[A/G]AAAGCTGAGAAAATT | 7468 |
rs776170464 | in-del | -/TG | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885667 | GCTGCTCTTCATGGC[-/TG]TGCCTTCTTGGTGGG | 7468 |
rs776253635 | in-del | -/TTA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936018 | CAATGAACCTAGATT[-/TTA]TTTAGTTTATTAGTA | 7468 |
rs776257489 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910460 | GGCTCAACCTTTTAA[A/G]TTGGAAACAGAAGAT | 7468 |
rs776275446 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | WHSC1 | GRCh38.p7 | 4:1935218 | GCTGAAGCTGAGGAC[A/G]CACCCAGGAAAAGAC | 7468 |
rs776310143 | snp | C/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937176 | CCTGCCTCAGACTCC[C/G/T]GAGTAGCTGGGATTA | 7468 |
rs776314100 | snp | C/T | 3.29609e-05 | 0.00405948 | intron-variant, utr-variant-3-prime, missense | WHSC1 | GRCh38.p7 | 4:1942379 | AGTTGGATTTGAACC[C/T]AGCTGCTCTGTACTG | 7468 |
rs776343672 | snp | C/T | 1.67452e-05 | 0.0028935 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951038 | CGCTGTGTTCTGCGA[C/T]TAGTGAACTGTCATC | 7468 |
rs776356849 | snp | C/T | 1.6591e-05 | 0.00288015 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916868 | TTTTATTTTAAAAAC[C/T]AGGTCAGAAAAAGAG | 7468 |
rs776362477 | snp | C/T | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1893840 | GTGAGCCACTGCACC[C/T]GGCCCTTGCCTCATG | 7468 |
rs776365029 | snp | C/G | | | intron-variant, downstream-variant-500B | WHSC1 | GRCh38.p7 | 4:1949224 | AAAGAACAGGATGTG[C/G]GCTGTGGCTCTTGCA | 7468 |
rs776384661 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956939 | TAGGAGTGCATGGTG[C/G]GCATTCAGAGATCTC | 7468 |
rs776435793 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906414 | TGGCTAATTTTTGTG[G/T]TTTTTTTGTAGAGAT | 7468 |
rs776441781 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1931447 | GATTTGTGATAAATA[C/T]GTGCTTGGATGTAAA | 7468 |
rs776465441 | in-del | -/AA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964966 | ATAAATAAAAATAAC[-/AA]AAACAGCAAACCTAG | 7468 |
rs776475452 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1958217 | GGGGGGATCTGCATG[C/G]GGGTTCTTGGATCCG | 7468 |
rs776479135 | snp | C/T | 3.53263e-05 | 0.00420261 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956227 | GTGAGACAGCACTCT[C/T]GTGCATTTTCTTACC | 7468 |
rs776510919 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970618 | ACCCCCAACACCGGC[A/G]AGCCAGAGCCGCTGA | 7468 |
rs776521258 | snp | C/T | 1.74111e-05 | 0.00295047 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978921 | ATAGCGCCAGGCGGC[C/T]GCTTGGCCGGATCCA | 7468 |
rs776553413 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943378 | GGTGCCTGGCCAGGA[C/G]TCCGTGGTTTCCTGT | 7468 |
rs776557868 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923120 | AGGAGCTTTGTCACC[A/G]TGGGAGAGGGAAGGA | 7468 |
rs776614044 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914803 | ATACCTTGCTATTCT[A/G]TTTCTTGTTCCATTA | 7468 |
rs776626819 | snp | A/G | 3.29968e-05 | 0.00406169 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1958021 | GCGCAAGCCCCCACC[A/G]TACAAGCACATCAAG | 7468 |
rs776629477 | snp | A/G | 3.34857e-05 | 0.00409167 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918491 | TACTCCTCAAAAGAC[A/G]GCAGAGGCTGACCCC | 7468 |
rs776652038 | in-del | -/AAAA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886838 | GCGAGACTCCATCTC[-/AAAA]AAAAAATAACTTGCT | 7468 |
rs776664584 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957177 | GCTGGCCTCCTTCTT[A/G]GGACGGATTGTAGGG | 7468 |
rs776698228 | snp | C/G | 1.71938e-05 | 0.002932 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917051 | AGGTGATAGATGACC[C/G]TTCAGTCTACTTTTA | 7468 |
rs776707784 | snp | G/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981370 | CCGTGGGTGTGGCTG[G/T]CTCTCGGCCCTGCCC | 7468 |
rs776718931 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960252 | CATTCCCTTAAAACA[G/T]GCCTTATGTCAGAAT | 7468 |
rs776718972 | snp | G/T | 1.71094e-05 | 0.00292479 | missense | WHSC1 | GRCh38.p7 | 4:1918596 | AGCATCCCAGTTTTT[G/T]GTCTTCTGTCAAAAA | 7468 |
rs776720335 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915829 | ATCTGGGCCAGTGTT[A/C]TGCATGAGGGGACAG | 7468 |
rs776751468 | in-del | -/AAAGTA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907535 | AAAAACTTTCAAGTC[-/AAAGTA]AAACAGCACAGCAGA | 7468 |
rs776755162 | snp | A/G | 3.30524e-05 | 0.00406511 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978687 | GTGTGGCAAACCTTC[A/G]ACTTCATTTTGCCAC | 7468 |
rs776756489 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911160 | ATGGGCTGTGATGGG[G/T]AAAAAAGGAACACAG | 7468 |
rs776781714 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1885389 | CTGATTCAGAAAAAA[C/T]AACAACAGAATGAAC | 7468 |
rs776785405 | in-del | -/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979717 | GGATAACTTTGTATA[-/T]TTTTTTTCATTTGGC | 7468 |
rs776811649 | in-del | -/TTATT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1879206 | CAACACTTTTTAAAA[-/TTATT]TTATTTTATTTTATT | 7468 |
rs776823034 | in-del | -/CCGCTTCCTGGGACCATGTTTATCCCAGTGTTTATCCCTGTTCACACACG | 1.779e-05 | 0.00298239 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974675 | CACGTGGTCCTGACC[lengthTooLong]TGTCCTCTGTGAGCA | 7468 |
rs776831475 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1967055 | GAAAAAAAGAGAAAA[G/T]ACTCACATAACTAAA | 7468 |
rs776841439 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933446 | GGCGGCTGGAGTGCA[A/G]TGGCGCGATCTCGGC | 7468 |
rs776864412 | in-del | -/CCT | 1.65236e-05 | 0.00287429 | cds-indel, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938508 | AGGCCATGGAGGCAG[-/CCT]CCTCCTCGCTCAAGA | 7468 |
rs776865727 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953331 | TTTGTTAGGGATTCA[C/T]TCATGTTTCGTGTGT | 7468 |
rs776867688 | snp | A/T | 0.000151638 | 0.0087061 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938443 | TTTTTTTTTTTTTTA[A/T]ATAATAGAGAGACAC | 7468 |
rs776885829 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884350 | ATCTGGCCCACCTTC[A/G]CCTCCCAAAGCACTA | 7468 |
rs776888983 | snp | A/C | 1.67444e-05 | 0.00289343 | missense | WHSC1 | GRCh38.p7 | 4:1901175 | GGAAGAGGAGCATAA[A/C]ATATGACTCCTTGCT | 7468 |
rs776894041 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1914192 | CGTGCCCAGCTCATT[G/T]TTGTATTTTTAGTAG | 7468 |
rs776919996 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953546 | GTGCACCTGCGCAGC[A/C]TTGCTGTGGGTTCAG | 7468 |
rs776977203 | snp | C/T | 8.47364e-05 | 0.00650854 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961188 | AGCTTCTGCAGTGTG[C/T]TGGACCTGGAGCCCT | 7468 |
rs777025421 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881652 | TCCTTCTGCCTGCAC[C/T]TCCCAAAGTTCTGGG | 7468 |
rs777035017 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972503 | GTGTCCTGGGGGTGA[C/T]AGTGTTCCCCATGGC | 7468 |
rs777066860 | snp | A/G | 3.74455e-05 | 0.00432682 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974635 | TGTCCTGTCCTCCCC[A/G]GCGCTCACTAAGGCT | 7468 |
rs777076556 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969432 | CAGCCAGGTGCAATG[G/T]CGTGTGCCTATAATC | 7468 |
rs777078587 | snp | A/G | 1.65026e-05 | 0.00287246 | missense | WHSC1 | GRCh38.p7 | 4:1978740 | AGGAGCACCAGGACG[A/G]GACAGCCTTCAGCTG | 7468 |
rs777084336 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982059 | TAAAAACTTGAAATT[C/T]ACTTTTTGGGGGGAG | 7468 |
rs777109234 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901467 | TGGCTGCTGAGCCAG[C/T]TGAGAGGTCTAGAGA | 7468 |
rs777124736 | snp | C/T | 1.66907e-05 | 0.00288879 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918188 | CCAGTGGGAAATGGG[C/T]ATTGTTCAAGCAGAA | 7468 |
rs777141363 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938921 | TGCATGTAAGCTAAC[A/G]GTAAGGGCTCGTTAT | 7468 |
rs777143375 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1973299 | GGCCCCGCTGGTAAT[A/G]GTAGGAATGTAGGTT | 7468 |
rs777172107 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970704 | AATGCTACTGATGAG[A/G]GCTGGGCTCTAGGGG | 7468 |
rs777180876 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1969542 | GGCCTTGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 7468 |
rs777212429 | snp | C/T | 1.7063e-05 | 0.00292082 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900696 | CCTTTCTGTTCAGAG[C/T]GTTGTAAAGTGCATA | 7468 |
rs777252662 | snp | A/G | 1.77947e-05 | 0.00298279 | missense | WHSC1 | GRCh38.p7 | 4:1900655 | AAGCATCTGGGCTGG[A/G]TGGAATTTAGCATCA | 7468 |
rs777256130 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936102 | AGTGCAGCATAGATA[C/T]AAAGCCAGCCCCGGG | 7468 |
rs777295950 | snp | A/T | 3.31219e-05 | 0.00406938 | missense | WHSC1 | GRCh38.p7 | 4:1955813 | GGAAGAAGCTGCACT[A/T]CCAGGATATCATTTG | 7468 |
rs777299282 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1972336 | CTGTGAGGGTGGAAA[A/T]CTTCCCCAGTGCAAG | 7468 |
rs777307335 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941193 | AAAATTAAATGAAAG[G/T]TCATTTACAGTTCCA | 7468 |
rs777325988 | snp | A/C/T | 7.59684e-05 | 0.00616275 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974619 | GGGAGCTCCAGCTCC[A/C/T]TGTCCTGTCCTCCCC | 7468 |
rs777352537 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964829 | AGAAAATTTAGAAAA[C/T]TAGACAGTGACTGCA | 7468 |
rs777393843 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952996 | CACTGGCCAGCTGCT[C/T]TCAAGGAGGAAAGGC | 7468 |
rs777436087 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966290 | CTCAAAGTAAATACA[G/T]GGTCAGCTATAAAAG | 7468 |
rs777484008 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1898778 | GCCTGGAATTTGGGC[-/AG]AGTTTATAGGCAGAA | 7468 |
rs777491915 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980894 | TTATGCTCCTTATGA[C/T]GCCCTAACTTGGAAG | 7468 |
rs777528421 | in-del | -/C | 0.000325321 | 0.0127497 | frameshift-variant | WHSC1 | GRCh38.p7 | 4:1956141 | GGAGGGGGACCGGGG[-/C]CAGCCGCTACCAGGG | 7468 |
rs777528706 | snp | A/G | 1.65562e-05 | 0.00287712 | missense | WHSC1 | GRCh38.p7 | 4:1918258 | TTCACCTTTCTCTAT[A/G]TGGGGGACCAGCTTC | 7468 |
rs777532117 | snp | A/G | 1.7187e-05 | 0.00293142 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935118 | GAGTGGTTTTCATGT[A/G]CATTTTCCCCATTCC | 7468 |
rs777540391 | snp | C/G | 8.24205e-05 | 0.00641899 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959584 | TGATTCGGAGTGTCT[C/G]AACAGGATGCTGATG | 7468 |
rs777582219 | snp | A/G | 1.69401e-05 | 0.00291029 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918143 | TTTTTTTTCCCAGCT[A/G]TTGAAACCAATTTCA | 7468 |
rs777590513 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970534 | GCCAGAAGGAGTGAT[-/G]GCGTACTCAGAATGT | 7468 |
rs777600254 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884209 | CAAGCCATCCTCCCA[A/C]CTCAGCCTCCCAAGT | 7468 |
rs777613380 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951222 | AGGAGAAGGCAGCAT[C/T]CGCTATGTCCGTGCT | 7468 |
rs777669998 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908958 | TGTCCCCAGCAGCCA[C/T]GGCTTTAGCAGTCCT | 7468 |
rs777673792 | snp | G/T | 1.64906e-05 | 0.00287142 | missense | WHSC1 | GRCh38.p7 | 4:1900756 | CAGTGCCAACGGGAA[G/T]ACTCCGAGCTGCGAG | 7468 |
rs777706302 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1965051 | TGTCCAGTGTTCAGC[-/A]AAAAAAAAAAAAAAA | 7468 |
rs777719842 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874971 | GGTTGCAATATTGCT[C/G]TTTTCTTTTGAGATA | 7468 |
rs777730489 | in-del | -/C | 6.88539e-05 | 0.00586705 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978912 | AGAGGGCAAATAGCG[-/C]CAGGCGGCCGCTTGG | 7468 |
rs777752754 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907477 | GATTCTAGCTTTTTT[-/T]GTGTATGTGTGAAAT | 7468 |
rs777753994 | in-del | -/GC | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964629 | ACAAAGAGGTGCGCT[-/GC]GCGCTGCCGTTGTTA | 7468 |
rs777758353 | snp | G/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892191 | CGCCATCACCATGTT[G/T]CCCAGTCTGGTCTCC | 7468 |
rs777763362 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937664 | GTGCATTCTCCTGTC[A/G]CCTTGTCCATGATCC | 7468 |
rs777777950 | snp | C/G | 1.65583e-05 | 0.00287731 | missense | WHSC1 | GRCh38.p7 | 4:1930749 | GCCCTGGTGGCCCCT[C/G]TCCAGGCTGAAGAAG | 7468 |
rs777823476 | snp | C/T | 4.18165e-05 | 0.00457236 | missense | WHSC1 | GRCh38.p7 | 4:1976479 | CTTGACTCTAGACCT[C/T]GACGACCCTTTCATC | 7468 |
rs777844512 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1932133 | CGCGCCCATGACCTC[A/G]GTGTTAGAAATCTAC | 7468 |
rs777859576 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874050 | GTCCTTTTTAGCTGG[A/G]CAAGTGGGCAAATAA | 7468 |
rs777866295 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922675 | TTACGCCTGTAATCC[C/T]AGCACTTTGGGAGGT | 7468 |
rs777895570 | snp | G/T | 1.69542e-05 | 0.0029115 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904423 | CTTTCTCTTCTGCAC[G/T]TAATCTTTCTCATCT | 7468 |
rs777935373 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882712 | GGGTTGAGCCAAGTA[A/C]CAGTTTTGGGCTTGT | 7468 |
rs777975691 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1918134 | GTGTCTCTTTTTTTT[C/T]TCCCAGCTATTGAAA | 7468 |
rs777987575 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979065 | CGCCTCCCCACCACT[A/G]AGCCATCCTCAGCAG | 7468 |
rs778041769 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942440 | TGCTGCAGGTGGCGT[A/G]TCATCGTACACACTC | 7468 |
rs778042555 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949594 | GGTGAAACCCCATCT[C/T]TACTAAAAATACAAA | 7468 |
rs778057489 | snp | G/T | 1.65075e-05 | 0.00287289 | missense | WHSC1 | GRCh38.p7 | 4:1959740 | GAGGGACATCAGAAA[G/T]GTATGTGTCGTTATC | 7468 |
rs778060997 | snp | A/G/T | 3.44366e-05 | 0.00414938 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955110 | GTTGCTCTTTTCACT[A/G/T]TGACTGGAGTCAGTG | 7468 |
rs778086860 | in-del | -/A | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944183 | AGTCCCATGTGTGGC[-/A]GCATTGTCCCACTTC | 7468 |
rs778096764 | snp | A/G | 1.68835e-05 | 0.00290542 | missense | WHSC1 | GRCh38.p7 | 4:1918538 | CTCCTCCTGGGAGGA[A/G]GAAGACCACAGTCTC | 7468 |
rs778131911 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957698 | CGACAGAACTCTGCC[C/T]TGGGCCTGTCTTGTA | 7468 |
rs778134392 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895543 | TTAATTTCAATACCA[A/G]TACTTTTTTTTTTCC | 7468 |
rs778149587 | snp | C/T | 3.30929e-05 | 0.0040676 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918434 | GGCCAAACTGTGTAG[C/T]TCTGCAGAGACCCTG | 7468 |
rs778165496 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930580 | AACAAAACCCAATGA[A/G]TTTTACGGATTTAAC | 7468 |
rs778180484 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1976837 | GGTGGCAGAGCCTTT[C/G]TTTGTTCCACCAGCC | 7468 |
rs778184509 | snp | C/G | 1.64814e-05 | 0.00287061 | missense | WHSC1 | GRCh38.p7 | 4:1900959 | AACTGCGTTTTGAGT[C/G]CCAGGAAATGAAAGG | 7468 |
rs778193524 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913815 | TGCCCAGCTGTCTTT[C/T]CTTCAATCTCTTTGT | 7468 |
rs778205471 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894531 | TACAAAAATTAGCCA[C/G]TGTGGTGGTGCATGC | 7468 |
rs778208479 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887462 | CTTGGTAGAGTGACA[A/G]AGAATTATTGACCAT | 7468 |
rs778222632 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883837 | ATGGCGATAAGAAGC[A/G]AGTGTGGCCCACATG | 7468 |
rs778224010 | snp | A/C | 1.75878e-05 | 0.0029654 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974703 | GCAAGAGAAACAGGA[A/C]TGGTTTGGGGGTGTC | 7468 |
rs778249129 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927431 | TCTAAAAAGATGTTG[A/G]GGGGAGCACAGTGCA | 7468 |
rs778277075 | snp | C/T | 1.6507e-05 | 0.00287284 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918380 | TGAAAACCCCAAGTC[C/T]GTGAGAGAAGAGTGC | 7468 |
rs778336591 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922818 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCTG | 7468 |
rs778358723 | in-del | -/TCTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968889 | AAGAGAATGTGATTC[-/TCTT]ACAGCCAAACAAATC | 7468 |
rs778359575 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952036 | GGAGACAGAAGCAGA[C/T]GGCTTCCCTTGTGGT | 7468 |
rs778377665 | snp | C/G | 3.29457e-05 | 0.00405854 | missense, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974885 | TAATAGACGCTGGCC[C/G]CAAAGGAAACTACTC | 7468 |
rs778402929 | snp | G/T | 3.32906e-05 | 0.00407973 | intron-variant | WHSC1 | GRCh38.p7 | 4:1957911 | TACTAAAATCTTTAC[G/T]CCTATTTCATTGACT | 7468 |
rs778411147 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942675 | AAGGCAGTCCCTTTA[G/T]TTGGGGGCTGTCCAG | 7468 |
rs778416669 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1880974 | ATAGTGGGTTTGTTA[G/T]GTTTAGTAATTCCTC | 7468 |
rs778426778 | snp | C/T | 1.69155e-05 | 0.00290817 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1955769 | CGAGATGCCTGACGG[C/T]AGCTGGTTCTGCAAT | 7468 |
rs778442161 | snp | A/C | 1.68244e-05 | 0.00290033 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939635 | ATTTGAAACTTTACA[A/C]ACCAAAATTATTTTA | 7468 |
rs778453999 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944143 | GCAGGGGCAAGTGAA[C/G]TCAGCACTCTGCAGT | 7468 |
rs778506416 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893043 | AGTCTTCTTCCTACA[A/G]CAGCACTTCTCCAGT | 7468 |
rs778513491 | snp | C/T | 1.67744e-05 | 0.00289602 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1952091 | GCGCTGCTTACCCGC[C/T]TGCTCTGCCCCCGCA | 7468 |
rs778536722 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911126 | TGAGCCCAGAGAGTC[A/G]CAAACTACCTGTAGT | 7468 |
rs778558019 | snp | C/T | 6.59587e-05 | 0.00574239 | missense | WHSC1 | GRCh38.p7 | 4:1900761 | CCAACGGGAAGACTC[C/T]GAGCTGCGAGGTGAA | 7468 |
rs778566589 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937852 | CAGCCCTTGAGAAAA[A/G]CTTCATGATCCCTTC | 7468 |
rs778568608 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1954492 | CTAAGCCTCTCAAGT[A/G]GCTGTGACCACGACG | 7468 |
rs778574014 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1963585 | TAGTAAAAAAGAAAT[-/G]GCCAGGTTGAGCATT | 7468 |
rs778644056 | snp | C/G | 1.64904e-05 | 0.00287139 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900864 | TAACGGCCACGACGC[C/G]CTGCCCTTTATTCCA | 7468 |
rs778656433 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980929 | TTCTAGGGACAGGCC[A/G]GGCAGTGTCCCCACA | 7468 |
rs778680904 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916399 | CACCCAGGCTGGAGA[A/G]CAGTGGTATGATCTT | 7468 |
rs778715134 | snp | A/T | 2.01035e-05 | 0.00317039 | | | GRCh38.p7 | 4:1976484 | CTCTAGACCTCGACG[A/T]CCCTTTCATCAGAGG | 7468 |
rs778733119 | snp | C/T | 5.07627e-05 | 0.00503774 | | | GRCh38.p7 | 4:1976618 | GCTGGTGCTGTGTGA[C/T]CGCAAGTTCTGCACC | 7468 |
rs778746453 | snp | C/T | 1.70029e-05 | 0.00291568 | | | GRCh38.p7 | 4:1935128 | CATGTACATTTTCCC[C/T]ATTCCCCATTCCAAG | 7468 |
rs778746567 | snp | C/G | 1.6563e-05 | 0.00287771 | | | GRCh38.p7 | 4:1952212 | AGAAGGGAGGTTCAC[C/G]TGCAGCGAGTGTGCC | 7468 |
rs778760069 | snp | A/G | | | | | GRCh38.p7 | 4:1939998 | ACACACGCACACAGT[A/G]TCTGTGTACATGTAC | 7468 |
rs778800591 | in-del | -/GTT | 3.34213e-05 | 0.00408773 | intron-variant | WHSC1 | GRCh38.p7 | 4:1904395 | TATTGTGTTCTTTGG[-/GTT]GTTTTTCCAACTTTC | 7468 |
rs778811508 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897865 | CTCCAGACCACAAGT[A/G]ATCCACCTGACTCAG | 7468 |
rs778821237 | in-del | -/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901591 | CGTCAGGCTACACTC[-/TT]TTCATGGATCTCATC | 7468 |
rs778847082 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911229 | TCTCTTCGAAGGGGA[-/T]TGTAGGTGGGGAGGT | 7468 |
rs778907234 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923711 | TACAGTTTTACTCCT[A/G]GATATTTACCCTAGA | 7468 |
rs778923970 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974367 | AGGCAGCCACCACCA[C/G]GCCCAGCTAATTTTT | 7468 |
rs778926682 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907184 | ATACCATCACCTTCA[C/T]GGAAAGGTCTTAATG | 7468 |
rs778951564 | snp | C/G | 1.65023e-05 | 0.00287244 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951080 | TCTCTAGGTCTCGGA[C/G]AGCCCGGGAGACGAG | 7468 |
rs778960672 | snp | G/T | 3.36757e-05 | 0.00410326 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961002 | GATTGGTCAGCACGC[G/T]TTTTGTCATGGCCAC | 7468 |
rs778974845 | snp | C/G | 1.71832e-05 | 0.00293109 | intron-variant | WHSC1 | GRCh38.p7 | 4:1955117 | TTTTCACTATGACTG[C/G]AGTCAGTGTTTGGGG | 7468 |
rs779013883 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962236 | TCGTGGGGCTTACAC[C/G]TTTCAAAGAAGTCAG | 7468 |
rs779038712 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971591 | ACAATAGTGCCGTGT[A/G]CTTTTCAGAGGCACA | 7468 |
rs779078036 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974961 | GTGGACAGTGAATGG[A/G]GACACTCGTGTGGGC | 7468 |
rs779089119 | snp | G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1944440 | TGAATTGCCGGTTGT[G/T]GAGGTGAATTTTGTT | 7468 |
rs779116189 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877097 | AGCCGAGATCATGCT[A/G]CTGCACTCCAGCCTG | 7468 |
rs779121408 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964980 | CAAAAACAGCAAACC[C/T]AGGGCAAGGGGAGGA | 7468 |
rs779124578 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1906269 | TTGGGGATGGAGGCT[C/T]GCTCCATCACCCAAA | 7468 |
rs779128866 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1972640 | CACCACTTATAAAGG[C/T]CAATTCCAGATGGAT | 7468 |
rs779132001 | snp | A/G | 4.94474e-05 | 0.00497205 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974822 | TTAAAAATAACATGC[A/G]ATTGCTAACACTTGA | 7468 |
rs779153388 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1959281 | CCTGCCTGCCTCTTG[C/T]GCTAAGAAGGCAGAG | 7468 |
rs779188095 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935658 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 7468 |
rs779189829 | snp | A/G | 1.65111e-05 | 0.0028732 | missense | WHSC1 | GRCh38.p7 | 4:1955274 | TGCACTGCCCACTTC[A/G]CTGCTCGGAAGGGGA | 7468 |
rs779204675 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922836 | GAGGCTGAGGCTGGA[A/G]AATTGCTTGAACCTG | 7468 |
rs779205776 | snp | A/G | 9.89332e-05 | 0.00703255 | missense | WHSC1 | GRCh38.p7 | 4:1957944 | TTAGCACTGCAAGAA[A/G]CTGAAGCTCGTTTTC | 7468 |
rs779212894 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1921338 | GTGGCGTGCGCCTGT[A/G]CTTCCGGCTATGTGG | 7468 |
rs779214255 | in-del | -/CA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874239 | TAGTCTTCTGAGCCT[-/CA]GTCTCTTGTTTTGCT | 7468 |
rs779214664 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957903 | CCTGTATTTACTAAA[A/G]TCTTTACTCCTATTT | 7468 |
rs779235854 | snp | A/G | 1.64933e-05 | 0.00287165 | missense | WHSC1 | GRCh38.p7 | 4:1901126 | CAGTCAGAAGAAAAT[A/G]GACAAAAACCAGAAA | 7468 |
rs779270976 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945671 | GTATAAGCATTTCCA[A/C]ATGAGGGAAAAGTCC | 7468 |
rs779293654 | snp | C/T | 8.52377e-05 | 0.00652775 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953196 | GAGCAAGGTTGGAAA[C/T]AGGGCCAGGTGCTTT | 7468 |
rs779341300 | snp | C/T | | | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1869657 | ATGCCTGGCACTGGC[C/T]GTAATTTTAAAAATT | 7468 |
rs779354867 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1883912 | ATGGTTTTCTACACA[A/G]TAGCCTAGGATAGAG | 7468 |
rs779367711 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1930789 | AACATAGCATTATGC[C/T]GATGTCCTCTGCTTG | 7468 |
rs779371197 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881221 | TAGCTGGGACACAGG[C/T]GTGTGCCACTACACC | 7468 |
rs779373817 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915283 | ACCATGCCTGGCTAA[A/T]TTTTGTATATTTAGT | 7468 |
rs779405995 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974578 | TGCTGACCTTAGCTC[C/G]CTTGTTTGCCATCAT | 7468 |
rs779422565 | snp | C/T | 3.29663e-05 | 0.00405981 | missense | WHSC1 | GRCh38.p7 | 4:1900949 | CACGATGCCAAACTG[C/T]GTTTTGAGTCCCAGG | 7468 |
rs779427014 | in-del | -/TC | 0.000142676 | 0.00844498 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918122 | GTGAAACTTACAGTG[-/TC]TCTTTTTTTTTTCCC | 7468 |
rs779428449 | snp | C/T | 1.79719e-05 | 0.0029976 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953266 | AGTGGCTCAGAACTG[C/T]AATTTAATTCTTGTT | 7468 |
rs779456515 | in-del | -/CT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924970 | TGTTAATGTCCAACA[-/CT]CTGCCCTGCCCACCC | 7468 |
rs779471481 | snp | C/T | 1.72698e-05 | 0.00293847 | intron-variant | WHSC1 | GRCh38.p7 | 4:1978635 | TCTTGTGTTCTGTTG[C/T]AGGGAAGTGGGAATG | 7468 |
rs779503775 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894850 | GTTCTATGGTCTTAA[-/G]TGCATTCACATTGTT | 7468 |
rs779513829 | snp | C/T | 0.000174444 | 0.00933764 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938423 | TTTTCTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 7468 |
rs779526894 | snp | A/G | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982680 | AGGGACTGGGTCCCC[A/G]GAGCAGGGAGGACAA | 7468 |
rs779548268 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927596 | TGGTGGTGCATGCCT[A/G]TAATCCCAGCTACTC | 7468 |
rs779643815 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882238 | TTGAAATGTGGTGTG[A/G]CCTGTGATTTGCTCT | 7468 |
rs779646081 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1899792 | CACGTGGGCCTCACT[A/G]GCCAGTGTGGTGCAC | 7468 |
rs779661761 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1900873 | CGACGCCCTGCCCTT[C/T]ATTCCAGCCGACAAG | 7468 |
rs779663094 | snp | A/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939853 | CGCTGCAGTGTGAGT[A/T]ATGCTCAGACTTCAT | 7468 |
rs779664157 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877102 | AGATCATGCTACTGC[A/C]CTCCAGCCTGGGCGA | 7468 |
rs779674908 | snp | C/G | 0.000102161 | 0.00714632 | missense | WHSC1 | GRCh38.p7 | 4:1976650 | AGGCCTACCACCTGT[C/G]CTGCCTGGGCCTTGG | 7468 |
rs779726491 | snp | A/G | 7.34754e-05 | 0.00606072 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1976510 | AGAGGAAAAGGGCAA[A/G]AAGACCAAGAAGAAA | 7468 |
rs779760306 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933844 | GCACTTACACCTTAC[C/T]GTCTTAGGTTGATAT | 7468 |
rs779773704 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1962385 | GGGGCAGTGGGAAAA[A/C]TTTTAATTTGGACAG | 7468 |
rs779776709 | in-del | -/TCA | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909361 | GGTCGCTGGTTGTGT[-/TCA]TTGCTCTGGGAGACA | 7468 |
rs779789612 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979324 | GCCCCCTTTCTGGCT[C/T]TCAGCGCCGTCGCCA | 7468 |
rs779826781 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904446 | TCTCATCTCCAGGCT[C/T]CTTTCTTACTCTTTC | 7468 |
rs779830910 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892505 | GCACTTATTTTAAAA[A/G]ACAGCAATGTGATGC | 7468 |
rs779856348 | snp | C/T | 0.000373925 | 0.0136683 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978910 | ACAGAGGGCAAATAG[C/T]GCCAGGCGGCCGCTT | 7468 |
rs779869088 | snp | A/G | 1.67024e-05 | 0.0028898 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916852 | CTTTCATTCTCTAAC[A/G]TTTTATTTTAAAAAC | 7468 |
rs779879571 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1970537 | CAGAAGGAGTGATGC[A/G]TACTCAGAATGTTGC | 7468 |
rs779906131 | in-del | -/TTC | | | downstream-variant-500B | WHSC1, NELFA | GRCh38.p7 | 4:1982421 | CTTTGGAAAAATGCT[-/TTC]TTCTTCTTTCAGAAA | 7468 |
rs779918919 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893239 | TTGGGAGTCCGAGAC[A/G]GGTAGATCACCTGAG | 7468 |
rs780003200 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1964458 | CTCTTGGCACAGCAG[C/T]GGCTACCCATGCCCC | 7468 |
rs780007384 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1911403 | GACCAGCCTGGCCAA[C/T]GTGATGAAACCCTGT | 7468 |
rs780008881 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1874220 | CAACTTTGGATAAGC[A/G]TTTTAGTCTTCTGAG | 7468 |
rs780015131 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1889211 | TCGTATATTAGTATT[A/T]TTTGAGACAGGGTCT | 7468 |
rs780017786 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1897643 | TTTTTATTTTTATTG[A/G]TATATTTTTGAGACA | 7468 |
rs780020577 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913662 | GGTGGACACATGACT[C/T]GCTTGACCTTACCTA | 7468 |
rs780035404 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895900 | GAGGGCCCAGCCCTG[A/G]GCTGGCTGGTAGAGG | 7468 |
rs780038851 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974977 | GACACTCGTGTGGGC[C/T]TGTTTGCCGTCTGTG | 7468 |
rs780080130 | in-del | -/AAAAT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924179 | TCTCTACCAAAAATA[-/AAAAT]AAAATAAAATGGTAT | 7468 |
rs780089837 | in-del | -/TTTC | 0.000239435 | 0.0109389 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938408 | TTCTTTTCTTTTTTT[-/TTTC]TTTCTTTCTTTTTTT | 7468 |
rs780103051 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1907422 | ATGTCCTCAGGTATT[C/G]CCTCAGTTTTCAAAA | 7468 |
rs780110565 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896393 | GCATTAGGCAGTGTA[A/G]CTAGACAAGGTCTTG | 7468 |
rs780113838 | snp | C/T | 1.67818e-05 | 0.00289665 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951035 | ACCCGCTGTGTTCTG[C/T]GACTAGTGAACTGTC | 7468 |
rs780126389 | snp | C/T | 5.42069e-05 | 0.00520582 | utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1900637 | ATAGTGTTCTAAGAA[C/T]GGAAGCATCTGGGCT | 7468 |
rs780144910 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922454 | TTATATATAGGAAGA[G/T]TCAAGCTTCTGAAGT | 7468 |
rs780161848 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1873752 | AAGTAGCTGGAATTA[-/G]GGCTTACTAAGCTAC | 7468 |
rs780182462 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927753 | AAAAAAAAAAAAGCC[A/G]TGTAGGGAGCAGGCA | 7468 |
rs780198150 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1895797 | ACATTTTTTGGTCTC[C/T]GGATTTAGCCTTCTT | 7468 |
rs780227146 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929543 | GTGAGCAGTGAGGGC[C/T]CTGTTCTGACTGCTC | 7468 |
rs780274468 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | WHSC1 | GRCh38.p7 | 4:1957960 | CTGAAGCTCGTTTTC[A/G]TGAAATTAAGCTTCA | 7468 |
rs780286540 | snp | C/G | 1.65113e-05 | 0.00287322 | missense | WHSC1 | GRCh38.p7 | 4:1901143 | ACAAAAACCAGAAAA[C/G]AAGGCGAGAAGGAAC | 7468 |
rs780287007 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1960540 | ATGACCCAGGTCCAT[A/C]CCAGGGCTGACCCAG | 7468 |
rs780333929 | snp | A/G | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891597 | GTGGCTCATGCCTGT[A/G]ATCCTAGCACTTTGG | 7468 |
rs780343459 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant, downstream-variant-500B | WHSC1, SCARNA22 | GRCh38.p7 | 4:1975051 | CTGGCTATGGGGGCA[A/G]AGTGGCCATCGCTGA | 7468 |
rs780344695 | in-del | -/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942021 | TTGGGTCACACCCCC[-/T]TTGCATGTTTGTATT | 7468 |
rs780346425 | snp | A/G | 3.29723e-05 | 0.00406018 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951090 | TCGGACAGCCCGGGA[A/G]ACGAGCCCTCGGAGT | 7468 |
rs780378776 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872776 | CAGCATCACGCATGG[A/G]TTATATTCACTCTAT | 7468 |
rs780380431 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1908887 | TGGGCTCAGGTCATC[A/T]TCTTCCTGCCTTGGC | 7468 |
rs780387498 | snp | G/T | 1.65778e-05 | 0.002879 | missense | WHSC1 | GRCh38.p7 | 4:1930664 | TTCAGGTGAGGAGAT[G/T]GAAGAGCTGCTCAGG | 7468 |
rs780423212 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917616 | TAATTTTTGTATTTT[C/T]AGTGGAGACAGGGTT | 7468 |
rs780434888 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916581 | GAAATCCTGAGCTCA[A/G]TCTCCCTGCCTCGGC | 7468 |
rs780440548 | snp | A/G | 1.828e-05 | 0.00302319 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930575 | TGCAAAACAAAACCC[A/G]ATGAGTTTTACGGAT | 7468 |
rs780445278 | in-del | -/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1961715 | GGAGTGCTCAGCTCT[-/G]GGCCTGATGCCCAAT | 7468 |
rs780454337 | snp | A/G | 1.65141e-05 | 0.00287346 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1959509 | CCAGATCTACACAGC[A/G]GATATTTCAGAAATC | 7468 |
rs780504979 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1954744 | TGTTAGGTGTGTGGG[A/G]TGAGGGTGGCAGGTT | 7468 |
rs780542767 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977868 | CGGTGGCTCATGCCT[C/G]TAATCCCAGCACTTC | 7468 |
rs780552913 | in-del | -/AGG | 1.66125e-05 | 0.00288201 | cds-indel | WHSC1 | GRCh38.p7 | 4:1978795 | CTGTGAGCATGACTT[-/AGG]GGCGGCATCGGTCAG | 7468 |
rs780564880 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887522 | GCTCCCTTGCGCAGG[C/T]GAGAGTACAGTGGCA | 7468 |
rs780569193 | in-del | -/AT | 0.000370276 | 0.0136015 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959435 | ATTCGGAAGGCTCTC[-/AT]GTGTGGACCAAGACA | 7468 |
rs780603171 | snp | C/T | 1.87933e-05 | 0.00306534 | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974633 | CCTGTCCTGTCCTCC[C/T]CGGCGCTCACTAAGG | 7468 |
rs780610748 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1950030 | TTTTGTGATGATTGA[A/G]GTGTACAGGAAATGT | 7468 |
rs780613752 | snp | A/G | 0.000359324 | 0.013399 | intron-variant | WHSC1 | GRCh38.p7 | 4:1976696 | TGGGTGTGCAGCCTC[A/G]CGGTGGCTTGCAGCT | 7468 |
rs780631652 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968241 | TGAGATCCAAGAAGT[A/C]ACAGTGAACAGACAA | 7468 |
rs780640478 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1913754 | CGCAGCCAGACATTC[A/G]GGGCCACTACCAGTC | 7468 |
rs780668193 | snp | C/G | | | intron-variant, upstream-variant-2KB | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974467 | GATCTGCCTGCTTCA[C/G]CCTCCCAAAGTGCTG | 7468 |
rs780674942 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1902640 | GACAGGGTCTTGGTA[C/T]GTTGCACAGGCTGTT | 7468 |
rs780689425 | in-del | -/TTTCTTTTTTTTTT | 0.000138696 | 0.0083264 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938413 | TTTCTTTTTTTTTTC[-/TTTCTTTTTTTTTT]TTTTTTTTTTTTTTT | 7468 |
rs780719363 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1927157 | GTGGCCCTCTCCACA[G/T]GGCTGCTGGTGTGTC | 7468 |
rs780723152 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1941757 | TTAGATAAATCTTCC[A/C]TTAGTGTTCATTTTT | 7468 |
rs780723431 | snp | C/T | 0.000132547 | 0.00813977 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938402 | CCTTTTTTTCTTTTC[C/T]TTTTTTTTTCTTTCT | 7468 |
rs780733114 | snp | C/T | 6.60186e-05 | 0.00574499 | missense | WHSC1 | GRCh38.p7 | 4:1978746 | ACCAGGACGGGACAG[C/T]CTTCAGCTGCACCCC | 7468 |
rs780748503 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945969 | AAAGCTTCCTCTGGC[C/T]AGGTAGACTTTTGTA | 7468 |
rs780756902 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1975827 | ATAAGAGCACTGGTC[C/T]TGTTGACTTAGCGCC | 7468 |
rs780777459 | in-del | -/T/TT | 0.0419438 | 0.138616 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918125 | AACTTACAGTGTCTC[-/T/TT]TTTTTTTTTTCCCAG | 7468 |
rs780819245 | snp | C/T | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980851 | TCTCCCAAAGTGTCC[C/T]AAGAAAATACTGGAT | 7468 |
rs780842954 | snp | C/T | 1.67685e-05 | 0.00289551 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961015 | GCTTTTTGTCATGGC[C/T]ACATGCTTGTGATTT | 7468 |
rs780891176 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1926262 | CAGGTTCAAACGATT[C/G]TCCTGACTCAGCCTC | 7468 |
rs780899920 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875816 | CGGGAGGCTGAGGCA[A/G]GAGAATGGCGTTAAC | 7468 |
rs780920728 | snp | C/T | 0.000110333 | 0.00742658 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953155 | TTGATGGCTGGATCT[C/T]TTTGCTGGAGAATGC | 7468 |
rs780940924 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971667 | AACATGGGAGGAGGG[A/G]ACCTGGGACCTGTGA | 7468 |
rs780944205 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951191 | GACTGCCAAAAAGGA[A/G]TATGTGTGCCAGGTG | 7468 |
rs780953841 | snp | A/G | 1.65285e-05 | 0.00287471 | missense, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938496 | ACAAGCTCTTACAAG[A/G]CCATGGAGGCAGCCT | 7468 |
rs781062101 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1882491 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAACA | 7468 |
rs781081947 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900136 | CTCTGCCTGATACCT[C/T]AGCTGTAACAGGAGG | 7468 |
rs781087646 | snp | C/T | 0.000179585 | 0.00947418 | intron-variant | WHSC1 | GRCh38.p7 | 4:1918114 | TTTGTGTAGTGAAAC[C/T]TACAGTGTCTCTTTT | 7468 |
rs781136611 | snp | A/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1980067 | TCACATGTGCCCTCT[A/G]CCAGGGCACCTACTG | 7468 |
rs781137263 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872711 | GCTCTTCAGTGCTAC[C/T]CACCTGCTTCACAGA | 7468 |
rs781156508 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887126 | TCCATGTGATGCCAG[C/G]TTGTTGGTACTGGCT | 7468 |
rs781172140 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1901327 | ATGAGGGCACCTGCA[C/T]GAGTACTGGGGCGGG | 7468 |
rs781172948 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966470 | GATCATCCTGGTTAA[C/G]ACGGTGAAACCCCAT | 7468 |
rs781174112 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1971304 | GACACAGAAGAAGGC[-/T]TTTTTTGACACCAGA | 7468 |
rs781197852 | snp | C/T | 3.82643e-05 | 0.00437387 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1978958 | GTGCAGGGCGGCCGG[C/T]CCTGCCTGCGGGAGA | 7468 |
rs781198289 | snp | C/G/T | 6.59178e-05 | 0.00574066 | missense, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951099 | CCGGGAGACGAGCCC[C/G/T]CGGAGTCCCCATACG | 7468 |
rs781235816 | snp | C/T | | | intron-variant, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952486 | GGCAGGGTGGCGGGA[C/T]GACAGGTCATGGGCT | 7468 |
rs781246841 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896521 | CTGTAGATGTGCGCC[A/G]GTGTGCCTGGCTAAT | 7468 |
rs781255847 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915112 | TTTTCTTTTTTTCTC[-/TTTTTTTTTTTTTT]TTTTTTTTGAGACGG | 7468 |
rs781266825 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934380 | ATGAGCCACCATGCC[C/T]GGCCTAGGAAAAGAT | 7468 |
rs781270209 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1886251 | TCACTGTGTGGCCAG[A/G]GCTGGAGTGTGGTGG | 7468 |
rs781282395 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1916788 | ACAACACCAAGGGAA[A/G]CAACTGCAAAATAGC | 7468 |
rs781355860 | snp | A/G | 1.68488e-05 | 0.00290243 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978813 | GGCGGCATCGGTCAG[A/G]AGCACCAAGACTGAG | 7468 |
rs781367586 | snp | C/T | 1.68122e-05 | 0.00289928 | missense, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1953500 | TGCCATGCTTCCAAC[C/T]CTTCAAACCCAAGGC | 7468 |
rs781398078 | snp | C/G/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1948573 | GTGGTGGGAAAAAGT[C/G/T]GGAATCTCTGCAATC | 7468 |
rs781409713 | snp | C/G | 1.73234e-05 | 0.00294302 | intron-variant | WHSC1 | GRCh38.p7 | 4:1935105 | AATGCAGCTTTTGGA[C/G]TGGTTTTCATGTACA | 7468 |
rs781458614 | snp | A/G | 3.29815e-05 | 0.00406075 | missense | WHSC1 | GRCh38.p7 | 4:1930713 | AGTGAGAAGCAGAGA[A/G]CACGCTACAACACCA | 7468 |
rs781475365 | snp | A/G | 1.65247e-05 | 0.00287438 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1978762 | CTTCAGCTGCACCCC[A/G]GACGGGCGGTCCTAC | 7468 |
rs781491226 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1968749 | AAGGAAAGGCTCCCA[C/T]AGGCCTTAATGTTTG | 7468 |
rs781497272 | snp | A/G | 1.64855e-05 | 0.00287097 | missense | WHSC1 | GRCh38.p7 | 4:1904252 | TGTCCAAACACTGGA[A/G]GAGACAAAGACCACC | 7468 |
rs781581830 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905900 | CGGTCAGTGTATGAA[A/T]AAATAAATGCTGGTT | 7468 |
rs781589450 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1898420 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCCAAGGC | 7468 |
rs781600443 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1939694 | TAAACCACTGAAGAA[A/G]CGAAATCGGGCTTCC | 7468 |
rs781607002 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1904598 | AGTGTTAAGGGACAC[A/C]TGACCTTTGCCTTGT | 7468 |
rs781616657 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1884403 | AGGCCCCTTTTGTTC[-/T]TTTTTTTTGAGACGG | 7468 |
rs781633390 | snp | C/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893354 | GCATGCCTGTAGTCT[C/T]AGCTACTCGGGAGGC | 7468 |
rs781660165 | snp | C/G | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942167 | TAAAAATTTTTATTG[C/G]AATAATTATTACATG | 7468 |
rs781677187 | snp | G/T | 1.65381e-05 | 0.00287555 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1939827 | TGGTATGAAGGCCAT[G/T]TAGCTGCCCACGCTG | 7468 |
rs781693360 | snp | C/T | 1.65105e-05 | 0.00287315 | synonymous-codon | WHSC1 | GRCh38.p7 | 4:1918401 | AGAAGAGTGCATTCC[C/T]ATGAAGAGAAGGCGG | 7468 |
rs781733824 | in-del | -/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1917957 | GGCTTATCTTTTGTA[-/TT]TTAGTAGAGATGGGG | 7468 |
rs781745914 | in-del | -/GAAGGG | 7.88418e-05 | 0.00627811 | cds-indel | WHSC1 | GRCh38.p7 | 4:1978855 | AGAGCCAGGGAAGCC[-/GAAGGG]GAAGAGGCGGCGGCG | 7468 |
rs781769841 | snp | A/G | 1.75434e-05 | 0.00296165 | intron-variant, nc-transcript-variant | WHSC1, SCARNA22 | GRCh38.p7 | 4:1974711 | AACAGGACTGGTTTG[A/G]GGGTGTCCTGTCTCA | 7468 |
rs796084991 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1877141 | GATTCTGTCTCAAGG[-/A]AAAAAAAAAAATTGT | 7468 |
rs796103051 | in-del | -/GT | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1945390 | CCTTGCTTGCCCATG[-/GT]GTGTGTGTCCAGAGG | 7468 |
rs796144446 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905132 | GAAACTCTGTCTCAC[-/A]AAAAAAAAAAAGAAT | 7468 |
rs796168850 | in-del | AA/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1977805 | CAAAAAAAAAAAAAA[AA/C]CAAACAAACAAAAAA | 7468 |
rs796251994 | in-del | -/TGTT | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981847 | AGTGTAGTTGATGAC[-/TGTT]TGTTAGTCAGTAGAG | 7468 |
rs796261936 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1875738 | AACCCCGTTTCTACT[-/A]AAAAAAAAAAAATAC | 7468 |
rs796274777 | in-del | G/TT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1887913 | GTTCCTTTTTTTCTT[G/TT]TTTTTTCTTCTGTGA | 7468 |
rs796306507 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933143 | TCACACCAGGCTGGA[A/G]CTGCAGCTGGTGAGG | 7468 |
rs796387210 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966876 | AAAAGGATGGGGACA[A/G]AGCTGTAAAGGGGCA | 7468 |
rs796490762 | snp | C/G | | | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979084 | CATCCTCAGCAGCGT[C/G]CGCTGCGTCTGCACT | 7468 |
rs796513046 | in-del | CC/TCCTTCCTCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1896680 | CTCCCTCCCTCCCTC[CC/TCCTTCCTCT]TTCCTTCCCGAACTC | 7468 |
rs796523656 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1957288 | GTTTTTTTGTTTTTG[-/T]TTTTTTTTTTTTTGA | 7468 |
rs796537672 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1949767 | AGACTCTGTCTCGAG[-/A]AAAAAAAAAAAAAAG | 7468 |
rs796578599 | snp | A/C | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872625 | GAGAGAGAGAGAGAG[A/C]GAGAGAGAGAGCGCG | 7468 |
rs796647728 | in-del | -/TGTCT | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1937549 | AAAAAGAAGTAATGG[-/TGTCT]TGTCTCTTCAGATTT | 7468 |
rs796652916 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1966696 | ACATTTAAAAAACAA[C/T]TACTAGTTTAAAAGC | 7468 |
rs796665455 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1881372 | GGTTTACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 7468 |
rs796671128 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1929622 | ATGCATGGGGCTGAC[A/T]TCCAGTAAAACTTTG | 7468 |
rs796686805 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1915814 | AATATCCTTTGATTC[A/T]TCTGGGCCAGTGTTC | 7468 |
rs796742263 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923929 | CATACCCACAACTGA[A/G]TTTAACTTATCCCTT | 7468 |
rs796753925 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1947339 | GTCCTTGCTGCCACC[C/T]GCTTGGGGCTATGTG | 7468 |
rs796791609 | in-del | -/CTTAA | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946221 | AGCTGTTATTGGCTT[-/CTTAA]CTTCTAAAATTTGGG | 7468 |
rs796836019 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1905509 | TCCTGTGGGGGCAGC[A/G]TTGCTGCCCTTGCTA | 7468 |
rs796851564 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1928071 | TTTAAAAATAATTTC[-/T]TTTTTTTTTTTTTTT | 7468 |
rs796963495 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1909919 | GCTGTGATTACAGGC[A/G]TGAGTCACCGCGCCC | 7468 |
rs796992319 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934016 | AAAAGTAGCAAGTTG[-/T]TTTTTTTTTTTAAGT | 7468 |