SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1868 | snp | C/G | 0.225005 | 0.248747 | intron-variant | KAT2B | GRCh38.p7 | 3:20148918 | TACAGCAGTCAAGTA[C/G]TTTAATCTAACTTCT | 8850 |
rs939851 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | KAT2B | GRCh38.p7 | 3:20086259 | GCCTGGGTGACAGAG[C/T]GAGACACTGTCTCAA | 8850 |
rs966898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KAT2B | GRCh38.p7 | 3:20142085 | CTCTCAGCTAACACC[A/G]TGGGGATGAATTAGT | 8850 |
rs977162 | snp | A/G | 0.249886 | 0.25 | intron-variant | KAT2B | GRCh38.p7 | 3:20150014 | AAGTAGGCTATGATC[A/G]ACGAGATCTGCTAGA | 8850 |
rs1046039 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20154259 | ttaaaaattaatatt[A/T]tCTTATAGATATTGT | 8850 |
rs1061636 | snp | C/G | 0.264632 | 0.249571 | intron-variant | KAT2B | GRCh38.p7 | 3:20149235 | CCATATTTTTGGAGA[C/G]AGCCAGAGTCTTCTG | 8850 |
rs1062974 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20154262 | aaaattaatattttC[A/T]TATAGATATTGTGCA | 8850 |
rs1124376 | snp | A/G | 0.152334 | 0.230133 | intron-variant | KAT2B | GRCh38.p7 | 3:20067054 | GAGACAACATGGGGT[A/G]AAACACTGAGAAGCA | 8850 |
rs1138710 | snp | A/C | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20149456 | agctgtgattgcacc[A/C]ctgcacttcagcctg | 8850 |
rs1610186 | snp | G/T | 0.444 | 0.157683 | intron-variant | KAT2B | GRCh38.p7 | 3:20067152 | TCCCAGTACAAAGTA[G/T]ATTTTTATTTCTTTT | 8850 |
rs1879775 | snp | A/T | 0.254105 | 0.249966 | intron-variant | KAT2B | GRCh38.p7 | 3:20081607 | GCCCACCAAAAGGAA[A/T]AAACTTTGCCACAGC | 8850 |
rs1915919 | snp | C/T | 0.400325 | 0.199756 | intron-variant | KAT2B | GRCh38.p7 | 3:20042389 | ATGAGAACAGGACAC[C/T]GACTGTAGTAGGCAG | 8850 |
rs1915920 | snp | A/G | 0.172351 | 0.237636 | intron-variant | KAT2B | GRCh38.p7 | 3:20042513 | taaagaacttatgta[A/G]tcaaacaccacctgt | 8850 |
rs1915921 | snp | A/G | 0.123798 | 0.215808 | intron-variant | KAT2B | GRCh38.p7 | 3:20042583 | CTTGGTGGCCTTGGC[A/G]TTTCGCAGCCAAAGT | 8850 |
rs1915922 | snp | C/T | 0.311123 | 0.242413 | intron-variant | KAT2B | GRCh38.p7 | 3:20042587 | GTGGCCTTGGCGTTT[C/T]GCAGCCAAAGTGGGC | 8850 |
rs1915923 | snp | C/T | 0.499965 | 0.00419314 | intron-variant | KAT2B | GRCh38.p7 | 3:20047156 | actagggtgggagga[C/T]cacctgagcccactg | 8850 |
rs1986917 | snp | C/G | 0.45889 | 0.13735 | intron-variant | KAT2B | GRCh38.p7 | 3:20077030 | ATGTTCTTTGGAGCT[C/G]TGGTTTTGTGTAGTC | 8850 |
rs2001650 | snp | G/T | 0.0923359 | 0.194016 | intron-variant | KAT2B | GRCh38.p7 | 3:20041059 | GCAACAAAACCCCAA[G/T]GTAGCCCGGGAGCTC | 8850 |
rs2068477 | snp | C/T | 0.490943 | 0.0666801 | intron-variant | KAT2B | GRCh38.p7 | 3:20151086 | AAGACTCATCAAATC[C/T]CACACTAAATGTCCC | 8850 |
rs2068668 | snp | C/T | 0.123105 | 0.215401 | intron-variant | KAT2B | GRCh38.p7 | 3:20151209 | TTGAATAAAGCCTAT[C/T]TTGGTTAGAGTGTAT | 8850 |
rs2140084 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | KAT2B | GRCh38.p7 | 3:20076109 | atcatgagccccttt[C/T]gatcatacctgagtt | 8850 |
rs2140085 | snp | A/C | 0.216649 | 0.247765 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20136623 | AAAACTTTTATATTA[A/C]TATTCAGCAAGTGAT | 8850 |
rs2293139 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | KAT2B | GRCh38.p7 | 3:20095016 | ACATTATTTGCATAC[A/G]TTAGCCACCAGCCCA | 8850 |
rs2293140 | snp | C/T | 0.499918 | 0.00638925 | intron-variant | KAT2B | GRCh38.p7 | 3:20095119 | AAGACTTCAGTCCTA[C/T]AGGAGTTCAGAAATT | 8850 |
rs2293141 | snp | A/T | 0.499923 | 0.00618962 | intron-variant | KAT2B | GRCh38.p7 | 3:20095153 | TCTTATTACCAGTGA[A/T]CTTAAAGGATTGATG | 8850 |
rs2293142 | snp | G/T | 0.434253 | 0.168969 | intron-variant | KAT2B | GRCh38.p7 | 3:20095191 | TGATGAAAGAGGACC[G/T]TCCACTTAAAAATGG | 8850 |
rs2293143 | snp | A/C | 0.000161214 | 0.00897669 | synonymous-codon, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20095402 | AGTTTATTTCTATCT[A/C]TTTAAGGTGAGATTT | 8850 |
rs2365361 | snp | A/G | 0.369754 | 0.219451 | intron-variant | KAT2B | GRCh38.p7 | 3:20082305 | CTCCCAGAGTGTTGG[A/G]ATTACAGGCTTGAGC | 8850 |
rs2365362 | snp | A/T | 0.254105 | 0.249966 | intron-variant | KAT2B | GRCh38.p7 | 3:20082385 | ACTTTAGTAAATTTA[A/T]CATTAATATAATACC | 8850 |
rs2365363 | snp | A/T | 0.451483 | 0.148002 | intron-variant | KAT2B | GRCh38.p7 | 3:20085143 | TTGCTTGAGCCCAGG[A/T]GTTTGAGACTAGCCT | 8850 |
rs2365364 | snp | A/T | 0.490673 | 0.0676508 | intron-variant | KAT2B | GRCh38.p7 | 3:20085199 | TATGTCTATTAATTT[A/T]AAAAAAAAGTTTATA | 8850 |
rs2365365 | snp | A/T | 0.490673 | 0.0676508 | intron-variant | KAT2B | GRCh38.p7 | 3:20085200 | ATGTCTATTAATTTA[A/T]AAAAAAAGTTTATAA | 8850 |
rs2365367 | snp | C/T | 0.482979 | 0.0906686 | intron-variant | KAT2B | GRCh38.p7 | 3:20074585 | CTATCAGGGTTCTTT[C/T]ACTTCACACAGCAGA | 8850 |
rs2365368 | snp | C/G | 0.497558 | 0.0348586 | intron-variant | KAT2B | GRCh38.p7 | 3:20076202 | aactgggacaaagac[C/G]aagtatatttcatac | 8850 |
rs2365369 | snp | A/G | 0.497558 | 0.0348586 | intron-variant | KAT2B | GRCh38.p7 | 3:20076232 | ctataccacaAACAT[A/G]TATTTTAATATATAT | 8850 |
rs2365370 | snp | A/G | 0.239326 | 0.249772 | intron-variant | KAT2B | GRCh38.p7 | 3:20077488 | GTAGCCACTGGCCAC[A/G]TGAAATGTGTTTACT | 8850 |
rs2365371 | snp | A/C | 0.242488 | 0.249887 | intron-variant | KAT2B | GRCh38.p7 | 3:20077651 | ttgggttaatgtatt[A/C]ttaaaattatttcta | 8850 |
rs2365375 | snp | A/G | 0.369958 | 0.21934 | intron-variant | KAT2B | GRCh38.p7 | 3:20089544 | tagctgagattacag[A/G]cgtgcgccaccatgc | 8850 |
rs2365785 | snp | C/T | 0.441841 | 0.160303 | intron-variant | KAT2B | GRCh38.p7 | 3:20093273 | tctcactgtgggcaa[C/T]tggtactcaattctg | 8850 |
rs2365790 | snp | C/T | 0.409721 | 0.192325 | intron-variant | KAT2B | GRCh38.p7 | 3:20049127 | GGCCTCTCAAAGTGC[C/T]GGGATTACAGGTGTG | 8850 |
rs2365792 | snp | A/G | 0.439502 | 0.163061 | intron-variant | KAT2B | GRCh38.p7 | 3:20111264 | TTTACAGGTAAGGAA[A/G]GAAAGGCTAAATAGC | 8850 |
rs2365793 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | KAT2B | GRCh38.p7 | 3:20111902 | AAGAAACATTCCAAG[A/G]GGATGGGAGAAAAGA | 8850 |
rs2365794 | snp | C/T | 0.432063 | 0.171327 | intron-variant | KAT2B | GRCh38.p7 | 3:20114810 | ATGTTAAGGTGATTG[C/T]CACAGATAATTAGGG | 8850 |
rs2623075 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | KAT2B | GRCh38.p7 | 3:20066652 | GTGATCCTCCCACCT[C/T]GGCATCCCAAAGTGC | 8850 |
rs2623077 | snp | A/G | 0.469247 | 0.120128 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20069989 | AATTCTCTGTAATGA[A/G]CCATCCACCTCTTCA | 8850 |
rs2623079 | snp | C/G | 0.472709 | 0.11358 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20069953 | TGCAAAGATCTCAGA[C/G]GCCATGTTCTTGAAG | 8850 |
rs2661376 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | KAT2B | GRCh38.p7 | 3:20150654 | CTTCCTCTGGCCTTC[A/G]TAGAGTTTTTTCAAT | 8850 |
rs2661377 | snp | C/T | 0.12932 | 0.218944 | intron-variant | KAT2B | GRCh38.p7 | 3:20145588 | AGACAGTGAGGTTAT[C/T]CCTTTAATAAAAAAA | 8850 |
rs2661378 | snp | G/T | 0.225301 | 0.248777 | intron-variant | KAT2B | GRCh38.p7 | 3:20143517 | ctcagtaataggatt[G/T]ctgtgtggaatggta | 8850 |
rs2661379 | snp | A/T | 0.0988009 | 0.199095 | intron-variant | KAT2B | GRCh38.p7 | 3:20139230 | TAAGAACACATTTTT[A/T]AAAAAAAAGAAGTCT | 8850 |
rs2686313 | snp | A/C | 0.266819 | 0.249434 | intron-variant | KAT2B | GRCh38.p7 | 3:20132845 | AAACTATAAATTTGT[A/C]CCCTTCATCCATAAT | 8850 |
rs2686314 | snp | A/G | 0.142947 | 0.22592 | intron-variant | KAT2B | GRCh38.p7 | 3:20146582 | GGAAGACATAAAAGG[A/G]TAACATTTGCTGCCT | 8850 |
rs2686315 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | KAT2B | GRCh38.p7 | 3:20146516 | GGCAATAAAGCTTTC[A/G]AAGTTACTGCATTCT | 8850 |
rs2686316 | snp | A/T | 0.237303 | 0.249677 | intron-variant | KAT2B | GRCh38.p7 | 3:20145846 | CCAAAAGCCTACAGT[A/T]GTTAAAGCTTTACTA | 8850 |
rs2686317 | snp | A/G | 0.245346 | 0.249957 | intron-variant | KAT2B | GRCh38.p7 | 3:20145689 | ACACAACCATGACAT[A/G]AGCCATCACACTGAC | 8850 |
rs2686318 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20144846 | gttgtgccattgcac[C/T]ccagtctgggtgaca | 8850 |
rs2686320 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | KAT2B | GRCh38.p7 | 3:20071881 | CAGAAGGGAAACCCA[C/T]AGAACCGAAGAAGTT | 8850 |
rs2686321 | snp | G/T | 0.497749 | 0.0334707 | intron-variant | KAT2B | GRCh38.p7 | 3:20071810 | GGCACACTTGCAGGC[G/T]CCTCCAAGACTTCTG | 8850 |
rs2686322 | snp | C/T | 0.497749 | 0.0334707 | intron-variant, utr-variant-5-prime | KAT2B | GRCh38.p7 | 3:20071613 | GTAGCCAAGAGTGAA[C/T]ATGATGTAGCCTTCT | 8850 |
rs2686323 | snp | A/G | 0.499325 | 0.0183582 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20069775 | ttgggaggccaaggc[A/G]ggtggatcatgaggt | 8850 |
rs2886463 | snp | C/T | 0.454664 | 0.143571 | intron-variant | KAT2B | GRCh38.p7 | 3:20092667 | tgatccctttatcat[C/T]atataatgccctttt | 8850 |
rs2929389 | snp | A/G | 0.468349 | 0.121752 | intron-variant | KAT2B | GRCh38.p7 | 3:20069144 | CTCTCATGTTCATAC[A/G]CAATGAATATGTCAA | 8850 |
rs2929390 | snp | A/G | 0.468349 | 0.121752 | intron-variant | KAT2B | GRCh38.p7 | 3:20068969 | CCACCCTTATTGTGG[A/G]CCAACCTCTCTTAGT | 8850 |
rs2929391 | snp | C/T | 0.46974 | 0.119223 | intron-variant | KAT2B | GRCh38.p7 | 3:20068713 | CACTGACTCATTCTT[C/T]CAACAATATTTATTG | 8850 |
rs2929392 | snp | C/G | 0.46974 | 0.119223 | intron-variant | KAT2B | GRCh38.p7 | 3:20068579 | AATGAGTAAATTATA[C/G]AATATACTGGAGAAT | 8850 |
rs2929393 | snp | C/T | 0.357451 | 0.225731 | intron-variant | KAT2B | GRCh38.p7 | 3:20068531 | AGAAAGAAAAAAGGA[C/T]GAGTACAGGGAACTT | 8850 |
rs2929394 | snp | A/C | 0.497984 | 0.0316851 | intron-variant | KAT2B | GRCh38.p7 | 3:20068409 | TAGGTATCTAGTATA[A/C]GGGAAACACAGCTAG | 8850 |
rs2929395 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | KAT2B | GRCh38.p7 | 3:20068149 | AATTAGTCGGCATGG[C/T]GGTGCACACCTGTAA | 8850 |
rs2929396 | snp | A/G | 0.469247 | 0.120128 | intron-variant | KAT2B | GRCh38.p7 | 3:20068141 | GGCATGGTGGTGCAC[A/G]CCTGTAATCCCAGCT | 8850 |
rs2929398 | snp | C/T | 0.18325 | 0.240924 | intron-variant | KAT2B | GRCh38.p7 | 3:20058562 | CTCAGGAGAACAAAA[C/T]TGCCTGGGATTGAGA | 8850 |
rs2929399 | snp | C/T | 0.095934 | 0.196885 | intron-variant | KAT2B | GRCh38.p7 | 3:20058559 | AGGAGAACAAAACTG[C/T]CTGGGATTGAGATAG | 8850 |
rs2929400 | snp | C/T | 0.093777 | 0.195178 | intron-variant | KAT2B | GRCh38.p7 | 3:20055274 | AATTTGTTGAGTAAA[C/T]GGAAAAAGTTGACAT | 8850 |
rs2929401 | snp | C/T | 0.498437 | 0.0279115 | intron-variant | KAT2B | GRCh38.p7 | 3:20055243 | Atatcactgtctcca[C/T]attacagctgcgaaa | 8850 |
rs2929402 | snp | A/G | 0.488302 | 0.0755777 | intron-variant | KAT2B | GRCh38.p7 | 3:20054618 | ACAAACCTCGCAAAA[A/G]GCTGCACAAGCCAAG | 8850 |
rs2929403 | snp | C/T | 0.093777 | 0.195178 | intron-variant | KAT2B | GRCh38.p7 | 3:20054422 | CAAAATAAATGCATC[C/T]ATCTCCTTCACATCT | 8850 |
rs2929404 | snp | A/G | 0.186737 | 0.241863 | intron-variant | KAT2B | GRCh38.p7 | 3:20053074 | ACTTAACTATGAGTA[A/G]GTGTTGTTCCAGCTC | 8850 |
rs2929405 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | KAT2B | GRCh38.p7 | 3:20052150 | GCTGGCATTTAAGAA[C/T]AGACTGGAATGAGGC | 8850 |
rs2929406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20052070 | GCAGGTAACCACATG[C/T]ACAATTAGATGCTAG | 8850 |
rs2929407 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | KAT2B | GRCh38.p7 | 3:20044423 | TTTATTTATTTATTT[A/T]TTTTTTTAGGGAGAA | 8850 |
rs2929408 | snp | G/T | 0.357024 | 0.225933 | intron-variant | KAT2B | GRCh38.p7 | 3:20041477 | AGTAGCGCCCGCCGC[G/T]CTGGGCTGTCACTTT | 8850 |
rs2948078 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | KAT2B | GRCh38.p7 | 3:20049856 | ATTTGGCACCTTCTA[C/T]AGCCTGAGTAGGTGT | 8850 |
rs2948081 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20038055 | CACTTTGAATAGGTC[C/T]TGAAACCACGGGCCT | 8850 |
rs2948082 | snp | C/T | 0.497933 | 0.032082 | intron-variant | KAT2B | GRCh38.p7 | 3:20054287 | GGGTCTGCCACCATA[C/T]GCAGCTAATTTTTGT | 8850 |
rs2948083 | snp | A/G | 0.167484 | 0.23599 | intron-variant | KAT2B | GRCh38.p7 | 3:20055481 | AATTCCTCTAGATAC[A/G]TGCCCAGGAAATCCT | 8850 |
rs2948084 | snp | A/G | 0.488666 | 0.0744214 | intron-variant | KAT2B | GRCh38.p7 | 3:20055975 | TGGTAGTTAATTTCT[A/G]TTTATTGCTGAGGAG | 8850 |
rs2948085 | snp | C/T | 0.188 | 0.24219 | intron-variant | KAT2B | GRCh38.p7 | 3:20056627 | AGGAAAAGAGAAATA[C/T]GGTCAAAGAGAAACT | 8850 |
rs2948086 | snp | G/T | 0.1652 | 0.235179 | intron-variant | KAT2B | GRCh38.p7 | 3:20057674 | TCCAGGGTACTAGTT[G/T]CTAGGCCCCAGTGTC | 8850 |
rs2948087 | snp | C/T | 0.17138 | 0.237316 | intron-variant | KAT2B | GRCh38.p7 | 3:20057723 | CCTTTTCAGGGGTAA[C/T]GCATGCTTAGGTTTG | 8850 |
rs2948088 | snp | C/T | 0.105924 | 0.204309 | intron-variant | KAT2B | GRCh38.p7 | 3:20058166 | ATGGCACTCATAAAT[C/T]AAGGTATTCAGCCAG | 8850 |
rs2948094 | snp | C/T | 0.497776 | 0.0332724 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070116 | CTACATCAGCATCCC[C/T]ATAGCTACATCCCCC | 8850 |
rs2948095 | snp | C/T | 0.462253 | 0.132093 | intron-variant | KAT2B | GRCh38.p7 | 3:20069093 | TCTTGTTAATGTATT[C/T]TGTTAGTCTGACTGA | 8850 |
rs2948096 | snp | C/T | 0.476746 | 0.10529 | intron-variant | KAT2B | GRCh38.p7 | 3:20068142 | CGGCATGGTGGTGCA[C/T]ACCTGTAATCCCAGC | 8850 |
rs2948097 | snp | C/T | 0.497959 | 0.0318836 | intron-variant | KAT2B | GRCh38.p7 | 3:20063934 | aaaactaggtatctg[C/T]gtgcacaagaatgaa | 8850 |
rs3021408 | snp | C/T | 0.482842 | 0.0910197 | synonymous-codon, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20072338 | ACATTTACAAGACTC[C/T]TCGGCCTAAAAATGG | 8850 |
rs3062235 | in-del | -/GAGA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20096971 | agagagagagagaga[-/GAGA]aagagagtgggggaa | 8850 |
rs3086993 | in-del | -/GT | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20065571 | ATAAGAGCATTGACT[-/GT]TTTTTAAAGGACACA | 8850 |
rs3749180 | snp | G/T | 0.482893 | 0.0909217 | intron-variant | KAT2B | GRCh38.p7 | 3:20072497 | GTCTCACGCTACAAT[G/T]AACTCGTTATACTTT | 8850 |
rs3749182 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KAT2B | GRCh38.p7 | 3:20072093 | GCTACAGCTCACGCA[A/G]CTGACCCACACACTT | 8850 |
rs3749184 | snp | A/G | 0.138546 | 0.223781 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20153688 | ATAGAAAAGTGAGAC[A/G]TCTGCCATTCCCAAC | 8850 |
rs3749185 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20153731 | AACTAATATACAACC[A/G]TATAAATGAAGGCCA | 8850 |
rs3762631 | snp | A/G | 0.234692 | 0.249531 | intron-variant | KAT2B | GRCh38.p7 | 3:20139953 | ACCTAATTTTTACTT[A/G]ACACCTGTTTCTGTT | 8850 |
rs3762632 | snp | G/T | 0.418491 | 0.184691 | intron-variant | KAT2B | GRCh38.p7 | 3:20140123 | GAGAACTTCAAAGAA[G/T]CTTGTCTTGATTCCT | 8850 |
rs3762633 | snp | C/T | 0.365205 | 0.221884 | intron-variant | KAT2B | GRCh38.p7 | 3:20140184 | AGTAGATATTTGGTG[C/T]ATGGTGTTCATATGA | 8850 |
rs3762635 | snp | A/G | 0.139903 | 0.224452 | intron-variant | KAT2B | GRCh38.p7 | 3:20149369 | GGTGCAGTGGCACAC[A/G]CCTGAGGCCCCAGCT | 8850 |
rs3792279 | snp | C/G | 0.126909 | 0.217598 | intron-variant | KAT2B | GRCh38.p7 | 3:20113334 | CTCTGAGTCAAGGTA[C/G]AAAGAAGACTCCTCC | 8850 |
rs3792281 | snp | G/T | 0.143284 | 0.226079 | intron-variant | KAT2B | GRCh38.p7 | 3:20142307 | ACATTCCGTTGAATG[G/T]GTGATGGAGGTTTGG | 8850 |
rs3804560 | snp | C/T | 0.305186 | 0.243833 | intron-variant | KAT2B | GRCh38.p7 | 3:20128231 | CATTGTTAATTTACA[C/T]ATACACGCAAACATG | 8850 |
rs3804561 | snp | C/T | 0.488241 | 0.0757703 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20136429 | ACCAAATTTAAAATG[C/T]TATGTATGTGATGAT | 8850 |
rs3804562 | snp | C/T | 0.488363 | 0.0753851 | intron-variant | KAT2B | GRCh38.p7 | 3:20139536 | GCAGTGAACTGCTGG[C/T]GATGGTGCTGAAGTT | 8850 |
rs3804563 | snp | C/G | 0.481009 | 0.0955756 | intron-variant | KAT2B | GRCh38.p7 | 3:20140954 | AAGCCATTTTGCATT[C/G]TGGCCTCAATTATTG | 8850 |
rs3804564 | snp | A/G | 0.152667 | 0.230274 | intron-variant | KAT2B | GRCh38.p7 | 3:20141061 | TCCATTAGCCACCCC[A/G]TTCACTCAGCACACA | 8850 |
rs3804565 | snp | A/C | 0.460813 | 0.134379 | intron-variant | KAT2B | GRCh38.p7 | 3:20142877 | AGCATAATTGGGTAT[A/C]TATGTGCCTGTGTGT | 8850 |
rs3804566 | snp | C/T | 0.466204 | 0.125522 | intron-variant | KAT2B | GRCh38.p7 | 3:20142890 | ATCTATGTGCCTGTG[C/T]GTGTGTGTGTGTGTA | 8850 |
rs3804567 | snp | C/G | 0.469642 | 0.119404 | intron-variant | KAT2B | GRCh38.p7 | 3:20149684 | ACCCTTTAAAGTGAA[C/G]ACACATCTATATGCT | 8850 |
rs3804568 | snp | C/G | 0.39214 | 0.205661 | intron-variant | KAT2B | GRCh38.p7 | 3:20149782 | ACTCAGTCTAGAATT[C/G]TGAATGGAAGGCTGA | 8850 |
rs3804570 | snp | A/T | 0.469346 | 0.119947 | intron-variant | KAT2B | GRCh38.p7 | 3:20150563 | AAAGGACATGAAAAC[A/T]GAATAATTTAATGGT | 8850 |
rs3804572 | snp | A/G | 0.391024 | 0.206427 | intron-variant | KAT2B | GRCh38.p7 | 3:20151194 | TACAGATGTGATGAC[A/G]TACACTCTAACCAAG | 8850 |
rs3804573 | snp | C/T | 0.148326 | 0.228391 | intron-variant | KAT2B | GRCh38.p7 | 3:20151298 | GGATATTGATGCAAA[C/T]GAATTCCTTCCCATT | 8850 |
rs3804574 | snp | A/T | 0.253824 | 0.249971 | intron-variant | KAT2B | GRCh38.p7 | 3:20151322 | TCCCATTTGGGGATA[A/T]TGTACGTACATTTAC | 8850 |
rs3804575 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KAT2B | GRCh38.p7 | 3:20151372 | TCCCAATGTATTTGG[C/T]TATAGGTTTCTTTCC | 8850 |
rs3804576 | snp | G/T | 0.411256 | 0.191041 | intron-variant | KAT2B | GRCh38.p7 | 3:20151443 | GTAGTCAGAAGTGGG[G/T]TTTTTTTTTTCCCAT | 8850 |
rs3804577 | snp | C/T | 0.382085 | 0.212258 | intron-variant | KAT2B | GRCh38.p7 | 3:20151453 | GTGGGGTTTTTTTTT[C/T]CCCATTTGACTTATT | 8850 |
rs3811672 | snp | G/T | 0.138546 | 0.223781 | intron-variant | KAT2B | GRCh38.p7 | 3:20130520 | GTAATTTTAGAAAAA[G/T]ATGGCGTAATTTTTA | 8850 |
rs3811673 | snp | A/G | 0.499527 | 0.0153681 | intron-variant | KAT2B | GRCh38.p7 | 3:20130526 | TTAGAAAAAGATGGC[A/G]TAATTTTTATTTTCA | 8850 |
rs3811674 | snp | C/T | 0.34146 | 0.23267 | intron-variant | KAT2B | GRCh38.p7 | 3:20130658 | GGATACTTTGTCTTA[C/T]TACTTCCCAGAAAGG | 8850 |
rs3828348 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | KAT2B | GRCh38.p7 | 3:20072556 | TCATACAGAGGTACA[C/T]AGCATTCAAATTTGG | 8850 |
rs3828349 | snp | A/G | 0.499325 | 0.0183582 | intron-variant | KAT2B | GRCh38.p7 | 3:20072552 | ACAGAGGTACACAGC[A/G]TTCAAATTTGGTGAA | 8850 |
rs3828350 | snp | A/G | 0.170084 | 0.236883 | intron-variant | KAT2B | GRCh38.p7 | 3:20122989 | GTAATTCCCCTTGAT[A/G]AATATCACATCACAG | 8850 |
rs3828351 | snp | C/G | 0.355311 | 0.226737 | intron-variant | KAT2B | GRCh38.p7 | 3:20142742 | GCCTGGTGATGAAAT[C/G]TGCATTAGCAGAGGC | 8850 |
rs3828352 | snp | A/T | 0.166832 | 0.235761 | intron-variant | KAT2B | GRCh38.p7 | 3:20150481 | TCTGGCCCAAGCATG[A/T]CTTCTTGTTACCCAT | 8850 |
rs3840184 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20113818 | GTGCTGCCTTTTTTT[-/T]CCACTTGGCTTTAAT | 8850 |
rs3840185 | in-del | -/A | 0.320096 | 0.239972 | intron-variant | KAT2B | GRCh38.p7 | 3:20113938 | AAATTTGGTTCAGGG[-/A]AAAAATGAAGAAGAC | 8850 |
rs3840186 | in-del | -/AGA | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20113952 | AAAAAATGAAGAAGA[-/AGA]CCACTGATAGCTTCA | 8850 |
rs3840188 | in-del | -/GTGT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20121780 | tgtgtgtgtgtgtgt[-/GTGT]ATAGCCAAGCCCAGC | 8850 |
rs3840189 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20128496 | TTTTTGTTTTGTTTT[-/G]TTTTTTTTTGTTGCT | 8850 |
rs3840190 | in-del | -/T | 0.488424 | 0.0751925 | intron-variant | KAT2B | GRCh38.p7 | 3:20139801 | TTTCTAATCACTTTA[-/T]TTTTTTGACCATCTT | 8850 |
rs3840191 | in-del | -/A | 0.455977 | 0.141681 | intron-variant | KAT2B | GRCh38.p7 | 3:20150812 | TCTTACCCATCTCCT[-/A]AAAAAAGTTCGAAAA | 8850 |
rs3849534 | snp | A/G | 0.499154 | 0.0205497 | intron-variant | KAT2B | GRCh38.p7 | 3:20048413 | GATTTGTGATATAGC[A/G]CTGTTTAAGGTTTTT | 8850 |
rs3929322 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20066543 | ggcatagtgacacat[A/G]cctgtagtcccagct | 8850 |
rs3942473 | snp | C/T | 0.24932 | 0.249999 | intron-variant | KAT2B | GRCh38.p7 | 3:20075828 | GCTCCCAGGTTTAAT[C/T]GATTCTCATGCCTCA | 8850 |
rs3960789 | snp | A/G | 0.18325 | 0.240924 | intron-variant | KAT2B | GRCh38.p7 | 3:20061707 | ttgtagttttaattt[A/G]tattttcataCGtat | 8850 |
rs4020098 | snp | G/T | 0.486725 | 0.0803809 | intron-variant | KAT2B | GRCh38.p7 | 3:20088156 | cattcatttgttggg[G/T]tggacacttaggtaa | 8850 |
rs4241545 | snp | A/T | 0.182933 | 0.240836 | intron-variant | KAT2B | GRCh38.p7 | 3:20065713 | CATATCCTGCAAAAA[A/T]TACTGAAACAAGTAA | 8850 |
rs4241546 | snp | A/G | 0.432504 | 0.170857 | intron-variant | KAT2B | GRCh38.p7 | 3:20106070 | TGTGAACTAGGGCAG[A/G]TCAGTTTATTCCTGA | 8850 |
rs4308300 | snp | A/G | 0.332568 | 0.235971 | intron-variant | KAT2B | GRCh38.p7 | 3:20077803 | CAAAGGGATCTAACA[A/G]AGTGCTTTAGTTGGT | 8850 |
rs4345088 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KAT2B | GRCh38.p7 | 3:20125192 | GCTGGGCGCCGTGGC[A/G]GGCTCCAGAGGCTGA | 8850 |
rs4405940 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KAT2B | GRCh38.p7 | 3:20087072 | ggcgtgagccactgc[A/G]cctggctgagatttt | 8850 |
rs4407416 | snp | C/G | 0.429087 | 0.174436 | intron-variant | KAT2B | GRCh38.p7 | 3:20077711 | CTATTGAATTGTGCT[C/G]GTTTAGAATATTCTA | 8850 |
rs4417886 | snp | C/T | 0.153 | 0.230415 | intron-variant | KAT2B | GRCh38.p7 | 3:20067019 | ACAGTTGGAGTGCTG[C/T]GGGGCTGACAAAACT | 8850 |
rs4419399 | snp | A/G | 0.441705 | 0.160466 | intron-variant | KAT2B | GRCh38.p7 | 3:20093487 | GGTAGTTGGAAACCA[A/G]GAGTTGTGGTAAGGA | 8850 |
rs4420892 | snp | C/T | 0.486133 | 0.082104 | intron-variant | KAT2B | GRCh38.p7 | 3:20082324 | acaggcttgagccac[C/T]gcacccggccacggt | 8850 |
rs4435661 | snp | C/T | 0.424348 | 0.179172 | intron-variant | KAT2B | GRCh38.p7 | 3:20093094 | TTAATCCTCTTAACT[C/T]TCTGAAAATGCATTT | 8850 |
rs4435663 | snp | A/G | 0.207559 | 0.246371 | intron-variant | KAT2B | GRCh38.p7 | 3:20096177 | ATGCTTTAAGAGGAG[A/G]AATCAACATATTCCA | 8850 |
rs4586829 | snp | A/G | 0.43978 | 0.162738 | intron-variant | KAT2B | GRCh38.p7 | 3:20096025 | GGCAGAGGGAGGAAC[A/G]GGTATTTTAGGCCGT | 8850 |
rs4602410 | snp | A/G | 0.497803 | 0.033074 | intron-variant | KAT2B | GRCh38.p7 | 3:20074773 | ATCATTTAGGATTCA[A/G]CTCCAACTGCCTCTG | 8850 |
rs4858155 | snp | C/G | 0.43309 | 0.17023 | intron-variant | KAT2B | GRCh38.p7 | 3:20101528 | TACAGACCTAAAATT[C/G]TACTTGACTCTATAA | 8850 |
rs4858156 | snp | C/T | 0.138886 | 0.22395 | intron-variant | KAT2B | GRCh38.p7 | 3:20101990 | ATTAGAGCCCTCACT[C/T]AAAAAATGCAATGAC | 8850 |
rs4858751 | snp | C/T | 0.18325 | 0.240924 | intron-variant | KAT2B | GRCh38.p7 | 3:20062862 | aagtcctttgcccat[C/T]gtaaaatttcgttgt | 8850 |
rs4858752 | snp | C/T | 0.186105 | 0.241697 | intron-variant | KAT2B | GRCh38.p7 | 3:20068253 | CGCCTGCCTCGGCCT[C/T]CCAAAGTGCTGCAAT | 8850 |
rs4858753 | snp | A/G | 0.497776 | 0.0332724 | intron-variant | KAT2B | GRCh38.p7 | 3:20075412 | CTAGCTGGAGGTCCC[A/G]TAATTCATTTCGGTT | 8850 |
rs4858754 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | KAT2B | GRCh38.p7 | 3:20075442 | TCTGACATGACCTAC[C/T]TGGAGATAGCATCAC | 8850 |
rs4858755 | snp | C/G | 0.186105 | 0.241697 | intron-variant | KAT2B | GRCh38.p7 | 3:20075482 | GTTAAGGGCACAGTC[C/G]CACAATAGTGCTCCC | 8850 |
rs4858756 | snp | C/G | 0.483272 | 0.0899109 | intron-variant | KAT2B | GRCh38.p7 | 3:20075490 | cacagtcccacaata[C/G]tgctcccacttcaga | 8850 |
rs4858757 | snp | G/T | 0.498945 | 0.022939 | intron-variant | KAT2B | GRCh38.p7 | 3:20075547 | cctttgcttctgacc[G/T]accggctataaatca | 8850 |
rs4858758 | snp | C/T | 0.497151 | 0.037632 | intron-variant | KAT2B | GRCh38.p7 | 3:20075741 | CCCTCTCCAGGTGCA[C/T]GACCCCCCAGGCACC | 8850 |
rs4858760 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20097530 | AAAATAATGATTAAA[A/T]TTTTTTTTTAATTTT | 8850 |
rs4858762 | snp | A/G | 0.499866 | 0.0081858 | intron-variant | KAT2B | GRCh38.p7 | 3:20098463 | aatgagataatatat[A/G]tgaagaaccatgaag | 8850 |
rs4858763 | snp | C/G | 0.138886 | 0.22395 | intron-variant | KAT2B | GRCh38.p7 | 3:20098475 | TATGTGAAGAACCAT[C/G]AAGATTGTCTGTTGA | 8850 |
rs4858764 | snp | C/T | 0.432504 | 0.170857 | intron-variant | KAT2B | GRCh38.p7 | 3:20100868 | AGGCATGATAGCAGG[C/T]TTTTGATTAGCATTT | 8850 |
rs4858765 | snp | A/T | 0.139564 | 0.224285 | intron-variant | KAT2B | GRCh38.p7 | 3:20102094 | GTCTAAAGTGGGTAG[A/T]TCACTTGGGTCAGGA | 8850 |
rs4858766 | snp | C/T | 0.439641 | 0.162899 | intron-variant | KAT2B | GRCh38.p7 | 3:20103120 | TTTAAATTATATCTT[C/T]ATTTCCGTATCTTTC | 8850 |
rs4858767 | snp | C/G | 0.499539 | 0.0151687 | intron-variant | KAT2B | GRCh38.p7 | 3:20125445 | TTGGCAAACTATAAC[C/G]CACAGGCCACATTTT | 8850 |
rs4858768 | snp | A/G | 0.136166 | 0.22258 | intron-variant | KAT2B | GRCh38.p7 | 3:20132877 | TATTAACTCCTTACA[A/G]GATGGTGCATACAAC | 8850 |
rs4858769 | snp | C/T | 0.190833 | 0.242898 | intron-variant | KAT2B | GRCh38.p7 | 3:20132934 | TAAAGTGAATTTCAT[C/T]AGAAGACACATTTCT | 8850 |
rs4858770 | snp | C/T | 0.393987 | 0.204372 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20152931 | GAATGTGAGAGTTTA[C/T]TTTTATTTTATTCTG | 8850 |
rs5847040 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | KAT2B | GRCh38.p7 | 3:20043729 | AGATTTGCTTTTTTT[-/A]AAAAAAAAAAAAATT | 8850 |
rs5847041 | in-del | -/TG | 0.182614 | 0.240747 | intron-variant | KAT2B | GRCh38.p7 | 3:20065570 | GATAAGAGCATTGAC[-/TG]TTTTTTAAAGGACAC | 8850 |
rs5847044 | in-del | -/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20112167 | CTTTTTTTTTTTTTT[-/T]CCGTTCAATTTCTCC | 8850 |
rs6419825 | snp | C/T | 0.499897 | 0.00718776 | intron-variant | KAT2B | GRCh38.p7 | 3:20097747 | tcacattgtcggcca[C/T]gcttgtcttgaactc | 8850 |
rs6419826 | snp | C/T | 0.499897 | 0.00718776 | intron-variant | KAT2B | GRCh38.p7 | 3:20097768 | tcttgaactcctagc[C/T]tcaagtgatctcccc | 8850 |
rs6550307 | snp | A/G | 0.211516 | 0.24702 | intron-variant | KAT2B | GRCh38.p7 | 3:20056393 | ACCATAGGAGAAGCA[A/G]GTTTGGGTAAGAATA | 8850 |
rs6550339 | snp | C/T | 0.463234 | 0.130503 | intron-variant | KAT2B | GRCh38.p7 | 3:20092900 | agagatggggtttca[C/T]catattggacaggct | 8850 |
rs6550340 | snp | A/G | 0.463234 | 0.130503 | intron-variant | KAT2B | GRCh38.p7 | 3:20092922 | ggacaggctggtctc[A/G]aactcctgaccttgt | 8850 |
rs6550351 | snp | C/T | 0.489201 | 0.0726845 | intron-variant | KAT2B | GRCh38.p7 | 3:20121050 | TACAAACCCCAGCTA[C/T]GAAATAAATAGTTTT | 8850 |
rs6550355 | snp | C/T | 0.200801 | 0.245111 | intron-variant | KAT2B | GRCh38.p7 | 3:20124113 | ATCTTTCCATTTCCT[C/T]CTAGATGTCCAGTCT | 8850 |
rs6550356 | snp | A/G | 0.130351 | 0.219509 | intron-variant | KAT2B | GRCh38.p7 | 3:20125366 | GGGCCTGTAATGAGA[A/G]TTTGAATCTGTCATC | 8850 |
rs6550359 | snp | A/G | 0.488302 | 0.0755777 | intron-variant, downstream-variant-500B | KAT2B, MIR3135A | GRCh38.p7 | 3:20137950 | GTTTGAAACAGCCTG[A/G]GCAACATAGTGAGAA | 8850 |
rs6550360 | snp | A/G | 0.487871 | 0.076925 | intron-variant, downstream-variant-500B | KAT2B, MIR3135A | GRCh38.p7 | 3:20138132 | AGAAAATGTAATAAA[A/G]CAAAAGAAGGAAAGA | 8850 |
rs6550361 | snp | G/T | 0.481627 | 0.0940692 | intron-variant | KAT2B | GRCh38.p7 | 3:20138899 | GTTTGGATTTTGTTT[G/T]TTTGTTTGTTTTGAG | 8850 |
rs6550362 | snp | A/T | 0.488485 | 0.0749998 | intron-variant | KAT2B | GRCh38.p7 | 3:20139231 | GACTTCTTTTTTTTT[A/T]AAAATGTGTTCTTAT | 8850 |
rs6550363 | snp | A/G | 0.125182 | 0.216612 | intron-variant | KAT2B | GRCh38.p7 | 3:20139650 | tatataCTCTGAAGC[A/G]GTCTGTTATTATGGC | 8850 |
rs6550364 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | KAT2B | GRCh38.p7 | 3:20139866 | TTTGCTGAGAATCCT[A/G]GGGACCCCCTCACCA | 8850 |
rs6550365 | snp | A/C | 0.128632 | 0.218563 | intron-variant | KAT2B | GRCh38.p7 | 3:20139871 | TGAGAATCCTGGGGA[A/C]CCCCTCACCACTTTT | 8850 |
rs6550373 | snp | A/G | 0.249038 | 0.249998 | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154470 | TATGATCTGGTTGAT[A/G]ACCATCAATTGAATC | 8850 |
rs6550374 | snp | C/G | 0.358515 | 0.225221 | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154548 | ATAAAAAATCCATAG[C/G]TCATCAGTAAGAGAT | 8850 |
rs6762971 | snp | C/G | 0.497749 | 0.0334707 | intron-variant | KAT2B | GRCh38.p7 | 3:20072976 | ATTGAATGTTTACTG[C/G]TGGTTTCCCTTTCAA | 8850 |
rs6763170 | snp | A/G | 0.469346 | 0.119947 | intron-variant | KAT2B | GRCh38.p7 | 3:20073132 | ATTTAAAAAAATCAT[A/G]TGTTGTTTGAGTAGA | 8850 |
rs6763504 | snp | A/T | 0.456568 | 0.140818 | intron-variant | KAT2B | GRCh38.p7 | 3:20115548 | CTAGGTCAATGTGTA[A/T]TATGGGGGCTTGTGA | 8850 |
rs6763542 | snp | A/G | 0.45946 | 0.136478 | intron-variant | KAT2B | GRCh38.p7 | 3:20121732 | CATACACATATGCAT[A/G]TGTGTGTGTGTGTGT | 8850 |
rs6765791 | snp | C/G | 0.469247 | 0.120128 | intron-variant | KAT2B | GRCh38.p7 | 3:20073328 | GTTCTTGCTAAGGTA[C/G]TTGCTCTTTCCACCT | 8850 |
rs6768260 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20107017 | tatatatatatatat[A/T]ttttttttttttttt | 8850 |
rs6771367 | snp | A/T | 0.272511 | 0.248984 | intron-variant | KAT2B | GRCh38.p7 | 3:20118774 | aACtatatatataat[A/T]tatatatttatacgt | 8850 |
rs6771737 | snp | A/G | 0.456568 | 0.140818 | intron-variant | KAT2B | GRCh38.p7 | 3:20115381 | ATGCCTTCTGGAGTC[A/G]CAGTGATCCCAGAAA | 8850 |
rs6771941 | snp | G/T | 0.274393 | 0.248807 | intron-variant | KAT2B | GRCh38.p7 | 3:20115585 | CCTCTAATGCCTCCA[G/T]CAAAGAAAAAATGAT | 8850 |
rs6772372 | snp | C/G | 0.294064 | 0.246086 | intron-variant | KAT2B | GRCh38.p7 | 3:20087664 | tctctacccgtacct[C/G]acgttccaagtccct | 8850 |
rs6773122 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | KAT2B | GRCh38.p7 | 3:20045729 | gggcttcagagttca[A/G]gctaatctgaattca | 8850 |
rs6773913 | snp | A/G | 0.486133 | 0.082104 | intron-variant | KAT2B | GRCh38.p7 | 3:20089954 | agaagaacagcttgg[A/G]caacatagtgagaag | 8850 |
rs6774367 | snp | A/G | 0.272511 | 0.248984 | intron-variant | KAT2B | GRCh38.p7 | 3:20121585 | TGAGGCATCATTTTA[A/G]GGCAAAAAAGCATTG | 8850 |
rs6776870 | snp | C/G | 0.330016 | 0.236849 | intron-variant | KAT2B | GRCh38.p7 | 3:20110048 | TTTAAAAAAAAAAGT[C/G]AGGAGCATGAATAAA | 8850 |
rs6777250 | snp | A/C | 0.442926 | 0.158996 | intron-variant | KAT2B | GRCh38.p7 | 3:20090851 | ttcaagcaatcctcc[A/C]acctcagcctcctga | 8850 |
rs6777429 | snp | A/G | 0.466721 | 0.124627 | intron-variant | KAT2B | GRCh38.p7 | 3:20060894 | aggttgtaataaacc[A/G]tgatcatgccactgc | 8850 |
rs6779675 | snp | C/T | 0.443195 | 0.158668 | intron-variant | KAT2B | GRCh38.p7 | 3:20090614 | tctgttgtgtatttt[C/T]gcatccatgttcatc | 8850 |
rs6779730 | snp | A/G | 0.460925 | 0.134204 | intron-variant | KAT2B | GRCh38.p7 | 3:20047441 | ACTTCGTGAATCATG[A/G]GCATATAttttaaac | 8850 |
rs6779759 | snp | G/T | 0.228253 | 0.249052 | intron-variant | KAT2B | GRCh38.p7 | 3:20090697 | gtattagtataatgc[G/T]gaccttgtaaagtga | 8850 |
rs6782086 | snp | A/G | 0.4862 | 0.0819127 | intron-variant | KAT2B | GRCh38.p7 | 3:20087167 | atgactgtggttaac[A/G]ataatatctagtttc | 8850 |
rs6783444 | snp | G/T | 0.306431 | 0.243548 | intron-variant | KAT2B | GRCh38.p7 | 3:20091892 | aaatgctattatttt[G/T]gcaccaatccaatac | 8850 |
rs6783552 | snp | A/T | 0.442113 | 0.159977 | intron-variant | KAT2B | GRCh38.p7 | 3:20092202 | tattgtatttcattc[A/T]atctctactttcaca | 8850 |
rs6783606 | snp | A/G | 0.44333 | 0.158505 | intron-variant | KAT2B | GRCh38.p7 | 3:20108994 | ggtgccaaaaaagtt[A/G]gggacctctgccata | 8850 |
rs6784711 | snp | A/T | 0.486067 | 0.0822953 | intron-variant | KAT2B | GRCh38.p7 | 3:20087107 | aggatacaaaattac[A/T]gctggataggaagaa | 8850 |
rs6784715 | snp | A/G | 0.130694 | 0.219696 | intron-variant | KAT2B | GRCh38.p7 | 3:20087319 | gggtacctcataaat[A/G]tgtacaattatatgt | 8850 |
rs6785363 | snp | A/T | 0.226615 | 0.248904 | intron-variant | KAT2B | GRCh38.p7 | 3:20087952 | gctaattaaaaaaaa[A/T]tttttttttgtagag | 8850 |
rs6787734 | snp | C/T | 0.381786 | 0.212444 | intron-variant, nc-transcript-variant | KAT2B, MIR3135A | GRCh38.p7 | 3:20137605 | GCAGTGGTGCAATCT[C/T]AGTTCACTGCAGCCT | 8850 |
rs6787947 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | KAT2B | GRCh38.p7 | 3:20072820 | GGTTGAAACCTCAAC[C/T]AACTGGTTTAATGAT | 8850 |
rs6788286 | snp | A/G | 0.44306 | 0.158832 | intron-variant | KAT2B | GRCh38.p7 | 3:20090695 | tggtattagtataat[A/G]ctgaccttgtaaagt | 8850 |
rs6788814 | snp | A/G | 0.432504 | 0.170857 | intron-variant | KAT2B | GRCh38.p7 | 3:20109340 | gCATGTCAGTGTCTC[A/G]TTCTGtcactctgtc | 8850 |
rs6791385 | snp | A/C | 0.292008 | 0.246445 | intron-variant | KAT2B | GRCh38.p7 | 3:20094947 | TATGGAAACCTAAGA[A/C]GTTGACCCTATTAGG | 8850 |
rs6793122 | snp | G/T | 0.442926 | 0.158996 | intron-variant | KAT2B | GRCh38.p7 | 3:20056894 | TTGTCCTACAGGGTT[G/T]TTGGGAGGGGAACAT | 8850 |
rs6793573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT2B | GRCh38.p7 | 3:20049392 | TTTGATTCTTCTACC[C/T]GGGGAAAGTGGAAGG | 8850 |
rs6793985 | snp | C/T | 0.29175 | 0.246489 | intron-variant | KAT2B | GRCh38.p7 | 3:20094993 | ACCAGTACTGATTCT[C/T]AAAATATACATTATT | 8850 |
rs6796085 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20100654 | CAGTAAATTTTATTT[G/T]GCCTCCAAACTCTAT | 8850 |
rs6797245 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | KAT2B | GRCh38.p7 | 3:20050656 | ttaaaaCATTGCCAG[A/C]AATTTTCAGGAGGAA | 8850 |
rs6799196 | snp | A/G | 0.456803 | 0.140473 | intron-variant | KAT2B | GRCh38.p7 | 3:20142444 | GTATTATTTGTTCCA[A/G]CTGTGAAAAACCCCT | 8850 |
rs6799600 | snp | A/G | 0.11963 | 0.213316 | intron-variant | KAT2B | GRCh38.p7 | 3:20142841 | GGCACTATTTGAGAA[A/G]GCGCGAATAGGCTAT | 8850 |
rs6799887 | snp | C/G | 0.488363 | 0.0753851 | intron-variant | KAT2B | GRCh38.p7 | 3:20139401 | CATCAGCTTTCCTCA[C/G]CTGTAACTGTAGTGC | 8850 |
rs6800085 | snp | A/G | 0.439224 | 0.163383 | intron-variant | KAT2B | GRCh38.p7 | 3:20109510 | tttgtagagatgggc[A/G]tcttactatgttgcc | 8850 |
rs6800250 | snp | C/T | 0.386694 | 0.20932 | intron-variant | KAT2B | GRCh38.p7 | 3:20081339 | GGTTAGTGAGGGTCA[C/T]GGCACACAGTGACAG | 8850 |
rs6803142 | snp | C/T | 0.126909 | 0.217598 | intron-variant, downstream-variant-500B | KAT2B, MIR3135A | GRCh38.p7 | 3:20137921 | ccagggcaggaggat[C/T]gctgtgctcaggagt | 8850 |
rs6803231 | snp | C/T | 0.332799 | 0.23589 | intron-variant | KAT2B | GRCh38.p7 | 3:20073044 | GATGGCTCAGTAGGC[C/T]CTGCTGCAGTCACTC | 8850 |
rs6804701 | snp | A/T | 0.456568 | 0.140818 | intron-variant | KAT2B | GRCh38.p7 | 3:20119236 | agcctacacacatga[A/T]cttccccaaatcagt | 8850 |
rs6805100 | snp | C/G | 0.46137 | 0.133501 | intron-variant | KAT2B | GRCh38.p7 | 3:20047857 | ctgacctcaagtgat[C/G]tgtctgcctgcgcct | 8850 |
rs6805673 | snp | A/G | 0.465052 | 0.127485 | intron-variant | KAT2B | GRCh38.p7 | 3:20144312 | ttttttttttgagac[A/G]gcgtctcactctgtc | 8850 |
rs6805752 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | KAT2B | GRCh38.p7 | 3:20049357 | TTTGTGTGTTTGCCA[A/C]AGTGTTATGTCTCAC | 8850 |
rs6805830 | snp | A/T | 0.316485 | 0.240998 | intron-variant | KAT2B | GRCh38.p7 | 3:20049397 | TTCTTCTACCCGGGG[A/T]AAGTGGAAGGTAAGG | 8850 |
rs6805894 | snp | C/T | 0.176219 | 0.238865 | intron-variant | KAT2B | GRCh38.p7 | 3:20043295 | TAGGTGCTGGGCCTA[C/T]GACACACAGAATTTG | 8850 |
rs6806287 | snp | C/T | 0.311369 | 0.242351 | intron-variant | KAT2B | GRCh38.p7 | 3:20043707 | ACCTGGAGAGTGACA[C/T]TATCTCAGATTTGCT | 8850 |
rs6807771 | snp | A/C | 0.207864 | 0.246424 | intron-variant | KAT2B | GRCh38.p7 | 3:20119142 | cctttcctttttaat[A/C]aaaaaaatacttttg | 8850 |
rs6808352 | snp | G/T | 0.492435 | 0.0610346 | intron-variant | KAT2B | GRCh38.p7 | 3:20049416 | TGGAAGGTAAGGGAG[G/T]TCATTTTACTAGCAG | 8850 |
rs6808694 | snp | C/T | 0.496714 | 0.0404017 | intron-variant | KAT2B | GRCh38.p7 | 3:20144805 | ctttctttttctttt[C/T]ttttttttaagagga | 8850 |
rs6809650 | snp | A/C | 0.386504 | 0.209444 | intron-variant | KAT2B | GRCh38.p7 | 3:20089768 | ttggctaaatttatt[A/C]ctaggtatttgattg | 8850 |
rs7355958 | snp | A/G | 0.467744 | 0.122832 | intron-variant | KAT2B | GRCh38.p7 | 3:20058111 | CTTGACCACTCTTTA[A/G]TATTTGTTTTTTTGA | 8850 |
rs7428620 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20081891 | ctcatatatatatat[A/G]tataaatgtatatag | 8850 |
rs7428621 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20081899 | tatatatgtataaat[A/G]tatatagagagtctc | 8850 |
rs7609821 | snp | C/T | 0.432797 | 0.170544 | intron-variant | KAT2B | GRCh38.p7 | 3:20120290 | tggagtgcagtggtg[C/T]gatctcagctcactg | 8850 |
rs7610788 | snp | C/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20050327 | TTACACATAAAGGGC[C/T]CAAATCATgtttata | 8850 |
rs7610868 | snp | C/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20050410 | agctgtaggacattt[C/T]cagcatctcagaggg | 8850 |
rs7611279 | snp | A/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20050868 | GGAATTTGATAGTCA[A/T]ATTTGGAAGAACCCA | 8850 |
rs7612385 | snp | A/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20046214 | ATTTATGGAGAACCC[A/C]GTTGCTTGGGTTCTC | 8850 |
rs7614744 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | KAT2B | GRCh38.p7 | 3:20082496 | agcctccactcaaga[A/T]tcacatatctgttta | 8850 |
rs7617840 | snp | G/T | 0.489259 | 0.0724914 | intron-variant | KAT2B | GRCh38.p7 | 3:20120724 | AAAAATATCTCTTGA[G/T]CCTAGAAGCATTTCA | 8850 |
rs7618523 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20050467 | ggtaatccttattct[A/G]acttctattaccaga | 8850 |
rs7618597 | snp | A/C | 0.228253 | 0.249052 | intron-variant | KAT2B | GRCh38.p7 | 3:20093096 | AATCCTCTTAACTCT[A/C]TGAAAATGCATTTGT | 8850 |
rs7618816 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20050784 | tctcggctcactgca[A/G]gatctgcctcctggg | 8850 |
rs7619948 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20046010 | gtgatcttaggcaca[A/G]gtcacttagtttttc | 8850 |
rs7620041 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20046172 | CCTGGTGCTTTACTC[A/G]TATATCAGAGTCAGT | 8850 |
rs7620608 | snp | C/T | 0.498632 | 0.0261223 | intron-variant | KAT2B | GRCh38.p7 | 3:20053886 | tcaccgcgacttcca[C/T]ctccaggttcaagtg | 8850 |
rs7622447 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20046318 | agggcatggtggctt[A/G]tgcctgtaatcccag | 8850 |
rs7622463 | snp | G/T | 0.439363 | 0.163222 | intron-variant | KAT2B | GRCh38.p7 | 3:20106535 | AGTGAATTTAACAGA[G/T]TACAAAATAAGATTA | 8850 |
rs7623123 | snp | C/T | 0.256897 | 0.249905 | intron-variant | KAT2B | GRCh38.p7 | 3:20084296 | TCTTCCTCCACCTCA[C/T]TGTTTATTCTAGGAA | 8850 |
rs7624514 | snp | G/T | 0.200801 | 0.245111 | intron-variant | KAT2B | GRCh38.p7 | 3:20123124 | catagactctttact[G/T]agattcagcagttaa | 8850 |
rs7626405 | snp | C/T | 0.48818 | 0.0759629 | intron-variant | KAT2B | GRCh38.p7 | 3:20135356 | TATTAGAAAAAACTC[C/T]GAAAAAAGTGATTAG | 8850 |
rs7627847 | snp | C/T | 0.46703 | 0.124089 | intron-variant | KAT2B | GRCh38.p7 | 3:20065909 | TAGTAATATGGAGGC[C/T]GCATGTATTATTTAA | 8850 |
rs7628266 | snp | A/G | 0.488786 | 0.0740357 | intron-variant | KAT2B | GRCh38.p7 | 3:20053878 | atctcagctcaccgc[A/G]acttccatctccagg | 8850 |
rs7630299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20066251 | gtctgtgtctgtctc[C/T]aaatctccttcttct | 8850 |
rs7630581 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | KAT2B | GRCh38.p7 | 3:20096675 | TTTATATGACAAAAA[C/T]AGCTAAATTTTCCAG | 8850 |
rs7633812 | snp | A/C | 0.389527 | 0.207442 | intron-variant | KAT2B | GRCh38.p7 | 3:20067659 | ATCCTTGAATTCTTT[A/C]tttatttattttttt | 8850 |
rs7637059 | snp | G/T | 0.271432 | 0.24908 | intron-variant | KAT2B | GRCh38.p7 | 3:20069362 | ggtttgttatgtaga[G/T]tcccctggtacccta | 8850 |
rs7637456 | snp | A/G | 0.433527 | 0.169758 | intron-variant | KAT2B | GRCh38.p7 | 3:20110872 | CCTCCAGCGTCGTGC[A/G]GTGATGCTGAGGTGC | 8850 |
rs7638345 | snp | A/G | 0.497776 | 0.0332724 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070924 | tgaggcacaagaatc[A/G]cttgaacctgagagg | 8850 |
rs7639181 | snp | A/G | 0.333261 | 0.235728 | intron-variant | KAT2B | GRCh38.p7 | 3:20092249 | tatttatttatttga[A/G]atggagtgttgctct | 8850 |
rs7639282 | snp | A/G | 0.227959 | 0.249026 | intron-variant | KAT2B | GRCh38.p7 | 3:20092381 | ttacaagcatgtgcc[A/G]ccacatccagcttat | 8850 |
rs7640134 | snp | A/G | 0.330016 | 0.236849 | intron-variant | KAT2B | GRCh38.p7 | 3:20141518 | TGTCATCCCACGTCA[A/G]TTCCACTTGATACTT | 8850 |
rs7640544 | snp | C/T | 0.497776 | 0.0332724 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070877 | agctgggtgtggtgg[C/T]gcatgccagtaaccc | 8850 |
rs7640713 | snp | A/T | 0.0391387 | 0.134304 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20071009 | gagagactctgtata[A/T]aaaaaaaaaaaaacc | 8850 |
rs7641684 | snp | A/G | 0.365853 | 0.221536 | intron-variant | KAT2B | GRCh38.p7 | 3:20096403 | TGGTGGTGGAAATGG[A/G]TAGCAAAACTTCAGG | 8850 |
rs7642097 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | KAT2B | GRCh38.p7 | 3:20045422 | ctggcacgatcatag[C/T]tcactgcagccttga | 8850 |
rs7642107 | snp | A/T | 0.361053 | 0.22398 | intron-variant | KAT2B | GRCh38.p7 | 3:20066749 | ccaCTGCAccgcatt[A/T]aaaaaaaaaaatcag | 8850 |
rs7642569 | snp | C/T | 0.473174 | 0.112665 | intron-variant | KAT2B | GRCh38.p7 | 3:20141659 | TTTTTTGTTAGGCAT[C/T]ATCTACCTAACAGCC | 8850 |
rs7644277 | snp | A/T | 0.383439 | 0.21141 | intron-variant | KAT2B | GRCh38.p7 | 3:20096496 | TGCTACTGAGGGCAT[A/T]GTAGATTATGTTGTA | 8850 |
rs7645157 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20046229 | AGTTGCTTGGGTTCT[C/T]GGCAAGGTGCCACAT | 8850 |
rs7645350 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | KAT2B | GRCh38.p7 | 3:20067768 | caacctctgcctccc[A/G]ggttcaagcgattct | 8850 |
rs7647172 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KAT2B | GRCh38.p7 | 3:20103418 | tttatttttattttt[A/T]ttttttttagagatg | 8850 |
rs7647320 | snp | C/T | 0.200801 | 0.245111 | intron-variant | KAT2B | GRCh38.p7 | 3:20123159 | atgccacatttgcta[C/T]ctctctttctctctg | 8850 |
rs7647946 | snp | C/T | 0.499897 | 0.00718776 | intron-variant | KAT2B | GRCh38.p7 | 3:20098101 | aggtgtggttgtgtg[C/T]acctgtaaattccag | 8850 |
rs7648603 | snp | C/T | 0.462691 | 0.131387 | intron-variant | KAT2B | GRCh38.p7 | 3:20143335 | accacaatgtgatac[C/T]atctcacaccagtca | 8850 |
rs7651283 | snp | C/T | 0.221737 | 0.248397 | intron-variant | KAT2B | GRCh38.p7 | 3:20054049 | gtgatccatcctcct[C/T]ggcctcccaaagtgc | 8850 |
rs7652263 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KAT2B | GRCh38.p7 | 3:20120864 | GAAGAGGACCTTATA[A/G]TATAagaagtgccat | 8850 |
rs7652967 | snp | A/T | 0.312104 | 0.242163 | intron-variant | KAT2B | GRCh38.p7 | 3:20044427 | ccctaaaaaaaaaaa[A/T]aaataaaTAAATAAA | 8850 |
rs7653243 | snp | G/T | 0.440746 | 0.161604 | intron-variant | KAT2B | GRCh38.p7 | 3:20104887 | TTTTTTTGTTGTTTT[G/T]TTGTTTTTTTTTTTT | 8850 |
rs9310605 | snp | C/T | 0.444533 | 0.157025 | intron-variant | KAT2B | GRCh38.p7 | 3:20105556 | CTGAGGCGAGAGGAT[C/T]GCTTGAGCCCAGGAG | 8850 |
rs9310606 | snp | C/G | 0.439363 | 0.163222 | intron-variant | KAT2B | GRCh38.p7 | 3:20105594 | CCAGCCTGGGCAACA[C/G]AATGAGACTTCATCT | 8850 |
rs9310607 | snp | C/T | 0.432504 | 0.170857 | intron-variant | KAT2B | GRCh38.p7 | 3:20105655 | GTGTGGTGGCATGTG[C/T]CTGTGGTGGCATGAG | 8850 |
rs9310608 | snp | C/T | 0.450609 | 0.149185 | intron-variant | KAT2B | GRCh38.p7 | 3:20105770 | CCTACCACTGCACTC[C/T]GGCCTGGGTGACAGA | 8850 |
rs9310609 | snp | C/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20106452 | GTACACACACACACA[C/G]ACACACACACACATT | 8850 |
rs9310610 | snp | A/G | 0.00787626 | 0.0622583 | intron-variant, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20122838 | GGCAGCCAGCTGGTA[A/G]ACCTCTTCTGCTCTC | 8850 |
rs9310611 | snp | C/T | 0.172997 | 0.237846 | intron-variant | KAT2B | GRCh38.p7 | 3:20142203 | GCTATTTTAGATGGC[C/T]AACAAAGCAGTCAAC | 8850 |
rs9310612 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | KAT2B | GRCh38.p7 | 3:20143663 | gtagattggataaag[A/G]aaatgtagtacatat | 8850 |
rs9682835 | snp | A/C | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20107622 | agatcatgccattgc[A/C]ctccagcctggggca | 8850 |
rs9784390 | snp | A/G | 0.428635 | 0.174898 | intron-variant | KAT2B | GRCh38.p7 | 3:20079056 | acccagctaattttt[A/G]taattattattatta | 8850 |
rs9809740 | snp | C/T | 0.200801 | 0.245111 | intron-variant | KAT2B | GRCh38.p7 | 3:20123463 | attgaaacatattgt[C/T]tgcagctgtctttgc | 8850 |
rs9813441 | snp | A/G | 0.312104 | 0.242163 | intron-variant | KAT2B | GRCh38.p7 | 3:20044922 | TGTTAGCAGTTGTGG[A/G]ATTTTAACTTAATCA | 8850 |
rs9815395 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | KAT2B | GRCh38.p7 | 3:20114012 | TTATTTCTGTTTTTC[C/T]CCCATTTATTGGTGA | 8850 |
rs9816216 | snp | A/G | 0.466204 | 0.125522 | intron-variant | KAT2B | GRCh38.p7 | 3:20063307 | cctgaccttcccagc[A/G]tgctgggattataca | 8850 |
rs9817616 | snp | C/T | 0.466927 | 0.124269 | intron-variant | KAT2B | GRCh38.p7 | 3:20058386 | CTTGAACCTGGGAGG[C/T]GGACATTGCAGTGAG | 8850 |
rs9817632 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KAT2B | GRCh38.p7 | 3:20058411 | agtgagccgagattg[C/T]gccactgcaccgtag | 8850 |
rs9817728 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | KAT2B | GRCh38.p7 | 3:20058277 | agcctggccaacatg[A/G]tgaaaccccgtctct | 8850 |
rs9817735 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | KAT2B | GRCh38.p7 | 3:20058287 | acatggtgaaacccc[A/G]tctctattaaaaata | 8850 |
rs9819628 | snp | C/T | 0.207864 | 0.246424 | intron-variant | KAT2B | GRCh38.p7 | 3:20099345 | AGATGATGCGTATGC[C/T]GTGCAGCTGCTGTAG | 8850 |
rs9819739 | snp | A/G | 0.208169 | 0.246476 | intron-variant | KAT2B | GRCh38.p7 | 3:20099268 | AATGAAAAAAAGACT[A/G]TAACAGTGAAAGTTG | 8850 |
rs9819915 | snp | A/G | 0.167484 | 0.23599 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20039156 | TGAGAAAAAGCCCTG[A/G]GCTTTTAAAACCTGC | 8850 |
rs9822453 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | KAT2B | GRCh38.p7 | 3:20051893 | CACACATGGGGTGTT[A/G]TATCTATTGCCATTT | 8850 |
rs9823780 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | KAT2B | GRCh38.p7 | 3:20076833 | TTTCAGTTGGTATAC[A/T]TTGTTGTTCTGTTTT | 8850 |
rs9824469 | snp | C/T | 0.0588605 | 0.161139 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20069882 | caaagttgtatattt[C/T]ggtttgccatattct | 8850 |
rs9826880 | snp | C/G/T | 0.029116 | 0.117091 | intron-variant | KAT2B | GRCh38.p7 | 3:20065313 | TGCACTCCCTAAAAG[C/G/T]TTGTCCTTCAGCTGG | 8850 |
rs9828532 | snp | A/G | 0.450734 | 0.149016 | intron-variant | KAT2B | GRCh38.p7 | 3:20107609 | ttgcagtgagtcgag[A/G]tcatgccattgccct | 8850 |
rs9828701 | snp | A/G | 0.208169 | 0.246476 | intron-variant | KAT2B | GRCh38.p7 | 3:20107711 | AAATATAATTTCACC[A/G]TGTAACCATTGTGAA | 8850 |
rs9829896 | snp | A/C | 0.290201 | 0.246747 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20135980 | ATTGGCCTACGTTGG[A/C]GGTGTTCTAGCAGAT | 8850 |
rs9832466 | snp | A/G | 0.162581 | 0.234218 | intron-variant | KAT2B | GRCh38.p7 | 3:20059489 | ttgggaggccgaggc[A/G]ggtggatcacgaggt | 8850 |
rs9835623 | snp | C/G | 0.0944967 | 0.195752 | intron-variant | KAT2B | GRCh38.p7 | 3:20042183 | tgatgctatgctagt[C/G]cacagaccacattCC | 8850 |
rs9836418 | snp | A/G | 0.211819 | 0.247067 | intron-variant | KAT2B | GRCh38.p7 | 3:20059700 | actgagcgagactcc[A/G]tctcaaaacaaaaac | 8850 |
rs9838973 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | KAT2B | GRCh38.p7 | 3:20085365 | AAAGATGACCCAGCA[A/G]ATGTTCTACCTAAGA | 8850 |
rs9840832 | snp | C/T | 0.176219 | 0.238865 | intron-variant | KAT2B | GRCh38.p7 | 3:20043112 | gtttcaccttgttgc[C/T]caggctgttctcaaa | 8850 |
rs9842739 | snp | C/T | 0.274929 | 0.248754 | intron-variant | KAT2B | GRCh38.p7 | 3:20068376 | GTTGAGCAAGCCAGG[C/T]ACTCTCTTGCCTTTG | 8850 |
rs9843017 | snp | C/G | 0.274393 | 0.248807 | intron-variant | KAT2B | GRCh38.p7 | 3:20068375 | TGTTGAGCAAGCCAG[C/G]CACTCTCTTGCCTTT | 8850 |
rs9844817 | snp | A/G | 0.432504 | 0.170857 | intron-variant | KAT2B | GRCh38.p7 | 3:20109242 | ACTGTTTAACTCTAT[A/G]GTTTCATTACTAGTT | 8850 |
rs9844824 | snp | C/G/T | 0.081446 | 0.184634 | intron-variant | KAT2B | GRCh38.p7 | 3:20049159 | gccaccgcgcctggc[C/G/T]GGGCATCGCcttaac | 8850 |
rs9846240 | snp | A/C | 0.218151 | 0.247963 | intron-variant | KAT2B | GRCh38.p7 | 3:20074146 | TGCCAGAAATTTAAT[A/C]TGTGTGTAAATTAAG | 8850 |
rs9847399 | snp | A/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20061834 | agtatataatatata[A/T]tatacataaaatata | 8850 |
rs9848075 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KAT2B | GRCh38.p7 | 3:20149825 | TATTGTCCACTATGT[A/G]CAAAATATGTTAAAA | 8850 |
rs9848249 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | KAT2B | GRCh38.p7 | 3:20127296 | CGAGATAGGGGCTAC[A/G]TGAAGGAAGTTTCTA | 8850 |
rs9849663 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | KAT2B | GRCh38.p7 | 3:20144996 | gaaatggggtttcac[C/T]gtgttggccaggctg | 8850 |
rs9849842 | snp | G/T | 0.153 | 0.230415 | intron-variant | KAT2B | GRCh38.p7 | 3:20040862 | cctcccgcttccacc[G/T]ccgcctcccgcctcc | 8850 |
rs9850104 | snp | C/T | 0.031825 | 0.122064 | intron-variant | KAT2B | GRCh38.p7 | 3:20050158 | tgagctgagatcata[C/T]cactgcactctagcc | 8850 |
rs9850217 | snp | A/G | 0.031825 | 0.122064 | intron-variant | KAT2B | GRCh38.p7 | 3:20050080 | tggcttgcacctata[A/G]tcccagctactcaga | 8850 |
rs9850294 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT2B | GRCh38.p7 | 3:20110499 | aacatagtgaaaccc[C/T]gtctttacaaaaaat | 8850 |
rs9851303 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | KAT2B | GRCh38.p7 | 3:20132863 | AAATTTATAGTTTCT[A/G/T]TTAACTCCTTACAAG | 8850 |
rs9851449 | snp | A/G | 0.483272 | 0.0899109 | intron-variant | KAT2B | GRCh38.p7 | 3:20074946 | ATGTTTCATGAGTAT[A/G]ATCCCATTTTATTAC | 8850 |
rs9852074 | snp | G/T | 0.311859 | 0.242226 | intron-variant | KAT2B | GRCh38.p7 | 3:20045298 | gctgggattacaggt[G/T]tgagccactgcacct | 8850 |
rs9853877 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KAT2B | GRCh38.p7 | 3:20151304 | TGATGCAAATGAATT[C/T]CTTCCCATTTGGGGA | 8850 |
rs9855900 | snp | C/T | 0.208169 | 0.246476 | intron-variant | KAT2B | GRCh38.p7 | 3:20105680 | catgagcctgtggtc[C/T]cagcgactctggagg | 8850 |
rs9856052 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | KAT2B | GRCh38.p7 | 3:20081522 | GCAAAGCCTCCCCTC[A/G]TCCCCTCACTTGCAC | 8850 |
rs9857135 | snp | A/G | 0.208169 | 0.246476 | intron-variant | KAT2B | GRCh38.p7 | 3:20106298 | CTTTTTAGTAGACCC[A/G]AAATCAGTCATGTAG | 8850 |
rs9859493 | snp | C/T | 0.00714247 | 0.0593314 | synonymous-codon, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20111614 | GCTGTGTTACTGCAA[C/T]GTGCCACAGTTCTGC | 8850 |
rs9860573 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | KAT2B | GRCh38.p7 | 3:20139992 | TTTAATATTTCTTGC[A/T]TTTTATTAGGGCCAT | 8850 |
rs9861556 | snp | C/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20076808 | ACGCAAGCCTGAATT[C/G]TCAAATACATTTCAG | 8850 |
rs9861831 | snp | A/T | 0.488424 | 0.0751925 | intron-variant | KAT2B | GRCh38.p7 | 3:20134806 | AATGCAAGTCACATA[A/T]GTAATTTCAAAATTT | 8850 |
rs9864695 | snp | C/T | 0.223225 | 0.248562 | intron-variant | KAT2B | GRCh38.p7 | 3:20079319 | AAGCTATTCTCCTGC[C/T]TCAGCCTCCCAAGTA | 8850 |
rs9864799 | snp | C/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20123416 | tgcaagccaaatctg[C/G]tccactggctgtttt | 8850 |
rs9865832 | snp | A/G | 0.0124887 | 0.078028 | intron-variant | KAT2B | GRCh38.p7 | 3:20147957 | TTTCACTTTGTTGAC[A/G]TATAGGAGAGACAGG | 8850 |
rs9867859 | snp | C/T | 0.046775 | 0.145601 | intron-variant | KAT2B | GRCh38.p7 | 3:20149914 | CCATCTCAGCTTCTT[C/T]TGGGAAACCCCCATG | 8850 |
rs9868770 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | KAT2B | GRCh38.p7 | 3:20088677 | gtgtgaaaatgttct[C/T]ttccattccataggt | 8850 |
rs9874446 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154691 | AATTAAAAGATTTTT[A/G]TTTTTATACTTTGCA | 8850 |
rs9874923 | snp | C/T | 0.466515 | 0.124985 | intron-variant | KAT2B | GRCh38.p7 | 3:20060071 | tcagcacttctttat[C/T]tttcattgcaagtaa | 8850 |
rs9875437 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | KAT2B | GRCh38.p7 | 3:20060438 | gaaaccctgtctcta[C/G]taaaaatacaaaatt | 8850 |
rs9877207 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | KAT2B | GRCh38.p7 | 3:20055517 | AGAAGGGACACGGAC[C/T]GAGGCCTGCATGATA | 8850 |
rs9878045 | snp | C/T | 0.309648 | 0.24278 | intron-variant | KAT2B | GRCh38.p7 | 3:20151608 | TCCTGACAGTGAGGA[C/T]TGAAGAAACCCTACT | 8850 |
rs9878933 | snp | A/G | 0.488363 | 0.0753851 | intron-variant | KAT2B | GRCh38.p7 | 3:20138528 | CTAAATATTTTAAAA[A/G]TTTCCATTTTTGTCA | 8850 |
rs9879926 | snp | G/T | 0.029116 | 0.117091 | intron-variant | KAT2B | GRCh38.p7 | 3:20060643 | acaaacTGTGGTAAT[G/T]ctgggcatggtagct | 8850 |
rs9881689 | snp | A/G | 0.039522 | 0.134904 | intron-variant | KAT2B | GRCh38.p7 | 3:20109007 | ttggggacctctgcc[A/G]tagagcctaggtgcc | 8850 |
rs9882626 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | KAT2B | GRCh38.p7 | 3:20049374 | GTGTTATGTCTCACG[A/T]CATTTGATTCTTCTA | 8850 |
rs9883707 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KAT2B | GRCh38.p7 | 3:20074179 | gtgccctcaaattaa[A/G]ctaaaaggacggtga | 8850 |
rs9884012 | snp | C/G/T | 0.0101771 | 0.0706052 | intron-variant, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20122844 | CAGCTGGTAGACCTC[C/G/T]TCTGCTCTCCTGGCC | 8850 |
rs9917784 | snp | A/G | 0.444533 | 0.157025 | intron-variant | KAT2B | GRCh38.p7 | 3:20100163 | TTTTAGGGTTGTTAC[A/G]TACTCACAGTTTACT | 8850 |
rs9917785 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | KAT2B | GRCh38.p7 | 3:20100212 | AACATTAAGTAGAAC[A/G]TGTAGTTTGTAAGAA | 8850 |
rs10084714 | snp | C/T | 0.163892 | 0.234703 | intron-variant | KAT2B | GRCh38.p7 | 3:20141840 | CTTTTTGTTCAAAGA[C/T]GTCAGCCTAAGAGAG | 8850 |
rs10428107 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20131118 | cctcctgggttctgg[A/T]gattctcctgcctca | 8850 |
rs10428249 | snp | C/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20131179 | agccaccatgcccgg[C/G]taatttttgtatttt | 8850 |
rs10510498 | snp | C/T | 0.14665 | 0.227637 | intron-variant | KAT2B | GRCh38.p7 | 3:20146809 | GCACATAGCCAGTAA[C/T]GGTCAGAATTAGAAG | 8850 |
rs10510499 | snp | A/G | 0.0505692 | 0.150756 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20153558 | TGTCAGTATTTTAAC[A/G]CCCACATTAGTATAT | 8850 |
rs10538060 | in-del | -/TATT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20045318 | CCACTGCACCTGGCC[-/TATT]TATTTATTTATTTAT | 8850 |
rs10554524 | in-del | -/AC | 0.482831 | 0.0910472 | intron-variant | KAT2B | GRCh38.p7 | 3:20106439 | AACAACACCAGAAGT[-/AC]ACACACACACACACA | 8850 |
rs10554735 | in-del | -/AGAAG | | | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154880 | AATCTAAACCAACTG[-/AGAAG]TTAAAAAAAAAAAAA | 8850 |
rs10558647 | in-del | -/TG | 0.402806 | 0.197864 | intron-variant | KAT2B | GRCh38.p7 | 3:20118329 | ATTTTCTCCTAAATT[-/TG]TGTGTGTGTGTGTGT | 8850 |
rs10583350 | in-del | -/TATTTATT | 0.151334 | 0.229706 | intron-variant | KAT2B | GRCh38.p7 | 3:20045318 | CCACTGCACCTGGCC[-/TATTTATT]TATTTATTTATTTAT | 8850 |
rs10584237 | in-del | -/GAGAA | 0.389527 | 0.207442 | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154879 | AAATCTAAACCAACT[-/GAGAA]GTTAAAAAAAAAAAA | 8850 |
rs10630876 | in-del | -/AG | 0.25214 | 0.249991 | intron-variant | KAT2B | GRCh38.p7 | 3:20096949 | AAAGAATAATAGGAA[-/AG]AGAGAGAGAGAGAGA | 8850 |
rs10634874 | in-del | -/CTT | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20139217 | CCAGCCAGACTTCTT[-/CTT]TTTTTTTAAAAATGT | 8850 |
rs10647897 | in-del | -/TTC | 0.497359 | 0.0362457 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070322 | TCTTTTTTTTTTTTT[-/TTC]TGAGATGGAGTCTCG | 8850 |
rs10652579 | in-del | -/TA | 0.461037 | 0.134028 | intron-variant | KAT2B | GRCh38.p7 | 3:20121691 | TTTCAAATATATAGC[-/TA]TATATATACATAATA | 8850 |
rs10662202 | in-del | -/AA | 0.438077 | 0.164702 | intron-variant | KAT2B | GRCh38.p7 | 3:20146672 | TATCCACCACTTAAT[-/AA]GAGTCTGCCATTTGT | 8850 |
rs10663947 | in-del | -/GA | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20142583 | AGAGAGAGAGAGAGA[-/GA]AAACTAGTATAGTTG | 8850 |
rs10675663 | in-del | -/TT | 0.476574 | 0.105661 | intron-variant | KAT2B | GRCh38.p7 | 3:20146670 | AATATCCACCACTTA[-/TT]ATGAGTCTGCCATTT | 8850 |
rs10706710 | in-del | -/A | 0.215144 | 0.247558 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20135666 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAATAA | 8850 |
rs10709834 | in-del | -/T | 0.378765 | 0.214288 | intron-variant | KAT2B | GRCh38.p7 | 3:20120214 | ACTTCTGCCACATTC[-/T]TTTTTTTTTTCCTTT | 8850 |
rs11128934 | snp | A/G | 0.425123 | 0.178415 | intron-variant | KAT2B | GRCh38.p7 | 3:20080823 | AACTTTTAATATTGC[A/G]TACGTATTGAAAGAA | 8850 |
rs11128935 | snp | C/T | 0.486266 | 0.0817214 | intron-variant | KAT2B | GRCh38.p7 | 3:20083901 | AGTCATTTTCCGTGA[C/T]GGTGGTGCACCTATT | 8850 |
rs11128936 | snp | A/T | 0.107341 | 0.205301 | intron-variant | KAT2B | GRCh38.p7 | 3:20092107 | tttaaagtatagttc[A/T]agcccagtgctttgt | 8850 |
rs11128937 | snp | C/T | 0.444533 | 0.157025 | intron-variant | KAT2B | GRCh38.p7 | 3:20099451 | GCTTCAGCACACCTA[C/T]AGTGGCCTGGATGGG | 8850 |
rs11128938 | snp | A/G | 0.444533 | 0.157025 | intron-variant | KAT2B | GRCh38.p7 | 3:20099452 | CTTCAGCACACCTAT[A/G]GTGGCCTGGATGGGC | 8850 |
rs11128939 | snp | G/T | 0.587989 | 0.124249 | intron-variant | KAT2B | GRCh38.p7 | 3:20099809 | GAGAGGAGAGAGAGA[G/T]AGACATACCAATTAA | 8850 |
rs11128940 | snp | A/G | 0.199254 | 0.244796 | intron-variant | KAT2B | GRCh38.p7 | 3:20117707 | TGGCTGTGTTGAAAC[A/G]TAGATGAACGTTCTC | 8850 |
rs11268707 | in-del | -/CGCAGTCTCGGCTGGAGTGCAGTGG | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20086841 | GCTGGAGTGCAGTGG[-/CGCAGTCTCGGCTGGAGTGCAGTGG]TGCAATCTCAGCTCA | 8850 |
rs11287582 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20107015 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 8850 |
rs11298850 | in-del | -/A | 0.414245 | 0.188477 | intron-variant | KAT2B | GRCh38.p7 | 3:20050200 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8850 |
rs11308672 | in-del | -/T | 0.499017 | 0.0221427 | intron-variant | KAT2B | GRCh38.p7 | 3:20086795 | TTAAAAACAAATAGA[-/T]TTTTTTTTTTTTTTG | 8850 |
rs11346744 | in-del | -/T | 0.498871 | 0.0237351 | intron-variant | KAT2B | GRCh38.p7 | 3:20085512 | TTTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTG | 8850 |
rs11391032 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20139060 | GCCCAGCAATTTTTT[-/T]TTTTTTAATCATTTG | 8850 |
rs11402275 | in-del | -/T | 0.488302 | 0.0755777 | intron-variant | KAT2B | GRCh38.p7 | 3:20138377 | TGTAGAAATAGAAAA[-/T]TATTTAACCAATACA | 8850 |
rs11403508 | in-del | -/A | 0.496842 | 0.0396107 | intron-variant | KAT2B | GRCh38.p7 | 3:20098234 | TAAAAAAAAAAAAAA[-/A]GTCAGTCTTAGATGT | 8850 |
rs11406998 | in-del | -/C | 0.48546 | 0.0840147 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20071018 | GTATATAAAAAAAAA[-/C]AAAACCAAAAAGTTT | 8850 |
rs11414280 | in-del | -/G | 0.471292 | 0.116318 | intron-variant | KAT2B | GRCh38.p7 | 3:20150884 | CCCCTCCCCCTTTTT[-/G]GGGGGGTACATGTTT | 8850 |
rs11417956 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20141794 | GCAAAGGCTTTTTTT[-/T]TTTTTTTGGAAAATA | 8850 |
rs11428295 | in-del | -/C | 0.21845 | 0.248001 | intron-variant | KAT2B | GRCh38.p7 | 3:20133429 | CTACATGTGACTAAT[-/C]ATTACCATATTGGAT | 8850 |
rs11705766 | snp | C/T | 0.309648 | 0.24278 | intron-variant | KAT2B | GRCh38.p7 | 3:20132313 | AGGAAGTGGAGGTTG[C/T]GGTGAGCCAAGATTG | 8850 |
rs11708763 | snp | C/T | 0.499527 | 0.0153681 | intron-variant | KAT2B | GRCh38.p7 | 3:20131180 | GCCACCATGCCCGGC[C/T]AATTTTTGTATTTTT | 8850 |
rs11712709 | snp | C/G | 0.158962 | 0.232835 | intron-variant | KAT2B | GRCh38.p7 | 3:20098285 | TAAACCCAATGGAAA[C/G]CTGCGTCCTAAAGTT | 8850 |
rs11712875 | snp | C/T | 0.00943375 | 0.0680285 | intron-variant | KAT2B | GRCh38.p7 | 3:20108640 | gtagaggtttgcagc[C/T]taagagcaatagact | 8850 |
rs11714203 | snp | C/T | 0.109461 | 0.206758 | intron-variant | KAT2B | GRCh38.p7 | 3:20101174 | AGAGATTTTTGTGAA[C/T]AGAGAAATGTCTGTT | 8850 |
rs11714225 | snp | C/T | 0.42263 | 0.180829 | intron-variant | KAT2B | GRCh38.p7 | 3:20080336 | ACCTCTGCCTTAGAT[C/T]TGGAAGCTCACACCA | 8850 |
rs11715447 | snp | A/C | 0.108755 | 0.206276 | intron-variant | KAT2B | GRCh38.p7 | 3:20098637 | CCCCCAAATGGGCCA[A/C]GTTCCTAAATGGTCT | 8850 |
rs11915701 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | KAT2B | GRCh38.p7 | 3:20120889 | tgccatatatttagc[A/T]tatgccaccattccc | 8850 |
rs11917197 | snp | C/T | 0.196666 | 0.245652 | intron-variant | KAT2B | GRCh38.p7 | 3:20139901 | TGGAGAAATTTGCAA[C/T]GGTCATATTTAATTA | 8850 |
rs11918156 | snp | A/T | 0.305186 | 0.243833 | intron-variant | KAT2B | GRCh38.p7 | 3:20112813 | ATTTTTATTATTCAG[A/T]TAGTGTTATTAGATT | 8850 |
rs11918735 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | KAT2B | GRCh38.p7 | 3:20101114 | CCACCGTGATCTGAG[A/G]CAAGATTCCCTCTGG | 8850 |
rs11920809 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | KAT2B | GRCh38.p7 | 3:20042667 | AAATTTATTTATTGG[A/G]TTCTCATCACCAGCA | 8850 |
rs11922657 | snp | C/T | 0.135825 | 0.222405 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20135816 | GGCTTGAAGGGCTGT[C/T]AAAAGCAGGAATGAG | 8850 |
rs11923928 | snp | A/G | 0.305436 | 0.243776 | intron-variant | KAT2B | GRCh38.p7 | 3:20111280 | GAAAGGCTAAATAGC[A/G]TAATCAAATTTTCAA | 8850 |
rs11926045 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | KAT2B | GRCh38.p7 | 3:20148086 | AACGGCAAACTAATT[A/G]TAATCACTAACACAA | 8850 |
rs11926387 | snp | A/C | 0.0126488 | 0.0785138 | intron-variant | KAT2B | GRCh38.p7 | 3:20101262 | TGCATAGCTGCATGA[A/C]GAAATTGCCTTCCCT | 8850 |
rs12106799 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KAT2B | GRCh38.p7 | 3:20093537 | TATTAGCAGCATCCT[C/G]TATCCCAGGCTTCTG | 8850 |
rs12485260 | snp | A/G | 0.173643 | 0.238054 | intron-variant | KAT2B | GRCh38.p7 | 3:20044404 | cctgggtgacagagc[A/G]agattctCCCtaaaa | 8850 |
rs12487645 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20130611 | CACTTTTAGGGATAC[C/T]AAAGGGAAACTGAAG | 8850 |
rs12488369 | snp | A/C | 0.186421 | 0.24178 | intron-variant | KAT2B | GRCh38.p7 | 3:20112567 | AGTTGATGACTTCTC[A/C]TGGAGCAGTAACAGC | 8850 |
rs12488589 | snp | C/G | 0.16028 | 0.233346 | intron-variant | KAT2B | GRCh38.p7 | 3:20140744 | tgatccacctgcctc[C/G]gcctcccaaattgtt | 8850 |
rs12490215 | snp | A/G | 0.273318 | 0.24891 | intron-variant | KAT2B | GRCh38.p7 | 3:20114693 | AGAGTAAACATTTGT[A/G]TAAATGCATTTCTGT | 8850 |
rs12490799 | snp | A/G | 0.172351 | 0.237636 | intron-variant | KAT2B | GRCh38.p7 | 3:20043050 | ggactacaggcatgc[A/G]ccagtacactattat | 8850 |
rs12490824 | snp | G/T | 0.172351 | 0.237636 | intron-variant | KAT2B | GRCh38.p7 | 3:20043148 | gagcccaagcaattt[G/T]cccgccttgcttccc | 8850 |
rs12492466 | snp | C/G | 0.173965 | 0.238157 | intron-variant | KAT2B | GRCh38.p7 | 3:20044644 | ctgggactggaagct[C/G]ttctttccacatttt | 8850 |
rs12493354 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KAT2B | GRCh38.p7 | 3:20045676 | CCATTTATATTAATA[C/T]GTAAGAGGAGGcaat | 8850 |
rs12630578 | snp | A/G | 0.137867 | 0.223442 | intron-variant | KAT2B | GRCh38.p7 | 3:20099530 | AAGCCAGAAACAGTG[A/G]GGAGAAGAGGGAAGT | 8850 |
rs12631220 | snp | C/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20100038 | TATCTCTATCTACGG[C/G]TTCCCTCCTCCATAC | 8850 |
rs12631457 | snp | G/T | 0.288127 | 0.247076 | intron-variant | KAT2B | GRCh38.p7 | 3:20116183 | ATGTTTCTTCTACAG[G/T]TGAGCAGTTAGCATT | 8850 |
rs12631479 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | KAT2B | GRCh38.p7 | 3:20116285 | TTACCTTGGATTTGA[C/T]CTCACCTAACTTTCA | 8850 |
rs12632127 | snp | C/G | 0.149665 | 0.228982 | intron-variant | KAT2B | GRCh38.p7 | 3:20066061 | CTGAGATCAAGATGT[C/G]ATCTGGGCCACACTC | 8850 |
rs12634506 | snp | A/G | 0.287085 | 0.247234 | intron-variant | KAT2B | GRCh38.p7 | 3:20092355 | cccatcagcctctca[A/G]gtagctgggattaca | 8850 |
rs12636032 | snp | A/G | 0.467744 | 0.122832 | intron-variant | KAT2B | GRCh38.p7 | 3:20063986 | gactgtcctttctct[A/G]ttgaatggtcttggc | 8850 |
rs12636078 | snp | A/G | 0.498673 | 0.0257246 | intron-variant | KAT2B | GRCh38.p7 | 3:20064181 | taatttgttattgtc[A/G]gctccttttgaAAAA | 8850 |
rs12636325 | snp | A/G | 0.254105 | 0.249966 | intron-variant | KAT2B | GRCh38.p7 | 3:20081941 | TATATGAGTCTCTAC[A/G]TATAAATTTGTTTTT | 8850 |
rs12636488 | snp | C/G | 0.0748431 | 0.178382 | intron-variant | KAT2B | GRCh38.p7 | 3:20052532 | AGGCTTTGTGAGATT[C/G]GTGGAAAGGAAACTG | 8850 |
rs12636856 | snp | A/G | 0.287346 | 0.247195 | intron-variant | KAT2B | GRCh38.p7 | 3:20095467 | ATGTACCCAGTCTCC[A/G]TATGCCAGGTCGTGG | 8850 |
rs12636894 | snp | C/T | 0.137527 | 0.223271 | intron-variant | KAT2B | GRCh38.p7 | 3:20123175 | CTCTCTTTCTCTCTG[C/T]GCCTCCCCATATGCT | 8850 |
rs12638247 | snp | C/T | 0.381503 | 0.21262 | intron-variant | KAT2B | GRCh38.p7 | 3:20059645 | gggaggtggagcttg[C/T]ggtgagccgagatcg | 8850 |
rs12639078 | snp | A/G | 0.384209 | 0.210922 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20038386 | CATTACCTAGACTCT[A/G]TTATATGGACCCCTA | 8850 |
rs12639214 | snp | A/G | 0.469544 | 0.119585 | intron-variant | KAT2B | GRCh38.p7 | 3:20143629 | aaagacatgaaatca[A/G]ttcaggtgcccatca | 8850 |
rs12639358 | snp | A/G | 0.24932 | 0.249999 | intron-variant | KAT2B | GRCh38.p7 | 3:20079260 | CCCAGGCTGGAGTGC[A/G]ATGGTGCAATCTCGG | 8850 |
rs13060230 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20061744 | aaaaataatatatat[A/G]aaaaaatatattata | 8850 |
rs13066876 | snp | C/G | 0.182296 | 0.240658 | intron-variant | KAT2B | GRCh38.p7 | 3:20063346 | accacacctggccgc[C/G]tgtgcttttggtatt | 8850 |
rs13066923 | snp | C/T | 0.182614 | 0.240747 | intron-variant | KAT2B | GRCh38.p7 | 3:20063441 | Attctttctttcttt[C/T]tttttttttcttttg | 8850 |
rs13069629 | snp | C/T | 0.139225 | 0.224118 | intron-variant | KAT2B | GRCh38.p7 | 3:20096770 | GCTCTTTTCTTTTCT[C/T]TGTCTGAACTTATTT | 8850 |
rs13072623 | snp | A/G | 0.398174 | 0.201356 | intron-variant | KAT2B | GRCh38.p7 | 3:20122064 | TGACTACAAGGAGAA[A/G]TAATCAAATCAACCA | 8850 |
rs13076204 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20134698 | aggcgtgagccacTA[A/G]GATTATAGGCCACCG | 8850 |
rs13076325 | snp | A/G | 0.432504 | 0.170857 | intron-variant | KAT2B | GRCh38.p7 | 3:20107128 | ACCTCCACCTCCTGG[A/G]TTCAAGCCATTCCCG | 8850 |
rs13076918 | snp | A/G | 0.432504 | 0.170857 | intron-variant | KAT2B | GRCh38.p7 | 3:20107368 | caatatataaaaaat[A/G]ccatttcagctggga | 8850 |
rs13077381 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20100430 | ACATTATGATTCCTG[A/G]AAAGAAGCCGTTTTA | 8850 |
rs13078078 | snp | A/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20064944 | GGATGCCACTCAAAT[A/C]TCTTCACACCCATCT | 8850 |
rs13078227 | snp | A/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20064958 | TATCTTCACACCCAT[A/C]TCACTCATTAACACT | 8850 |
rs13078370 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20064930 | TCTCCTGTTCCTCTG[A/G]ATGCCACTCAAATAT | 8850 |
rs13080058 | snp | A/T | 0.496874 | 0.0394129 | intron-variant | KAT2B | GRCh38.p7 | 3:20073721 | ACCTTTTTAAAAAAA[A/T]AAATAAATAAAACAG | 8850 |
rs13082298 | snp | A/T | 0.230017 | 0.2492 | intron-variant | KAT2B | GRCh38.p7 | 3:20078200 | taaataaataaataa[A/T]taaataaaAAGGCAG | 8850 |
rs13082384 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20061743 | aaaaaataatatata[G/T]gaaaaaatatattat | 8850 |
rs13082735 | snp | A/G | 0.448066 | 0.152544 | intron-variant | KAT2B | GRCh38.p7 | 3:20078211 | ATAAATAAATAAAAA[A/G]GCAGCCTGTTTTTAC | 8850 |
rs13083709 | snp | C/T | 0.288646 | 0.246995 | intron-variant | KAT2B | GRCh38.p7 | 3:20095778 | CAATATATATTTCAG[C/T]AGAAGAGACAGTCAA | 8850 |
rs13089721 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20063535 | ttctgAGTAGGCCTC[C/T]ttttttttttttttt | 8850 |
rs13090341 | snp | A/C | 0.132751 | 0.2208 | intron-variant | KAT2B | GRCh38.p7 | 3:20067024 | TGGAGTGCTGCGGGG[A/C]TGACAAAACTTTTAT | 8850 |
rs13090593 | snp | A/C | 0.143959 | 0.226396 | intron-variant | KAT2B | GRCh38.p7 | 3:20089995 | taaaaaacaaacaaa[A/C]aaaaaaacaaAACAA | 8850 |
rs13095603 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20131060 | tgctcttgttgccca[A/G]gctggagtgcaatgg | 8850 |
rs13095743 | snp | A/C | 0.186105 | 0.241697 | intron-variant | KAT2B | GRCh38.p7 | 3:20067663 | TTGAATTCTTTCTTT[A/C]TTTATTTTTTTATAT | 8850 |
rs13096186 | snp | A/G | 0.470521 | 0.117772 | intron-variant | KAT2B | GRCh38.p7 | 3:20067936 | TGCCTTAACCTCCCA[A/G]AGTTCTAGGATTACC | 8850 |
rs13096876 | snp | C/T | 0.136506 | 0.222754 | intron-variant | KAT2B | GRCh38.p7 | 3:20118713 | cctgggcgacaaaag[C/T]gaaactttgtctcaa | 8850 |
rs13097157 | snp | A/G | 0.139564 | 0.224285 | intron-variant | KAT2B | GRCh38.p7 | 3:20118647 | agaatagcttgaacc[A/G]gggaggcagaggagg | 8850 |
rs13097409 | snp | A/G | 0.136847 | 0.222927 | intron-variant | KAT2B | GRCh38.p7 | 3:20126338 | AACTTTATATTTTAC[A/G]TTGCTGATGACTCTC | 8850 |
rs13098588 | snp | A/G | 0.136166 | 0.22258 | intron-variant | KAT2B | GRCh38.p7 | 3:20086093 | ctggacaacatggtg[A/G]aaccccatctctaca | 8850 |
rs13098782 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20107050 | ttttttttttttttt[G/T]gagacggagtcttgc | 8850 |
rs13098901 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KAT2B | GRCh38.p7 | 3:20048700 | GTTAAGAGAAAAGTG[A/G]CTATTTAGGAAAAAT | 8850 |
rs13100028 | snp | A/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20073714 | ATAATTTACCTTTTT[A/T]AAAAAATAAATAAAT | 8850 |
rs13100730 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20064911 | CTAGACAGCTGGCTG[A/T]CTTTCTCCTGTTCCT | 8850 |
rs13100737 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20064928 | TTTCTCCTGTTCCTC[C/T]GGATGCCACTCAAAT | 8850 |
rs13100859 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20064943 | TGGATGCCACTCAAA[C/T]ATCTTCACACCCATC | 8850 |
rs13100868 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20064963 | TCACACCCATCTCAC[G/T]CATTAACACTGCGTG | 8850 |
rs13313945 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | KAT2B | GRCh38.p7 | 3:20132150 | gaggctgaggcgggc[A/G]gatcacctgaggttg | 8850 |
rs13317632 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | KAT2B | GRCh38.p7 | 3:20132164 | cggatcacctgaggt[C/T]gggagtttgagacca | 8850 |
rs13323791 | snp | A/G | 0.444533 | 0.157025 | intron-variant | KAT2B | GRCh38.p7 | 3:20100030 | TCCTTTTATATCTCT[A/G]TCTACGGCTTCCCTC | 8850 |
rs13323914 | snp | A/G | 0.444533 | 0.157025 | intron-variant | KAT2B | GRCh38.p7 | 3:20100367 | GTAAGTCAAGCAAAA[A/G]AAGCAAAAAAGAAAT | 8850 |
rs13326027 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | KAT2B | GRCh38.p7 | 3:20089549 | gagattacaggcgtg[C/T]gccaccatgcccggc | 8850 |
rs17006525 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | KAT2B | GRCh38.p7 | 3:20073752 | AACGAAACAAAACAA[C/T]CACTAACTCTGAATG | 8850 |
rs17006540 | snp | C/T | 0.101658 | 0.201233 | intron-variant | KAT2B | GRCh38.p7 | 3:20082973 | ACTCCCTGGGCCTTC[C/T]GTTGAATGCAGATCA | 8850 |
rs17006610 | snp | A/G | 0.274124 | 0.248833 | intron-variant | KAT2B | GRCh38.p7 | 3:20111071 | TTACTCAAAGGACTA[A/G]GTGGTTAATTCTGAT | 8850 |
rs17006623 | snp | G/T | 0.276194 | 0.248624 | intron-variant | KAT2B | GRCh38.p7 | 3:20119551 | TTTCTTGTTACCTAA[G/T]AAAGGAGTCAGTCAT | 8850 |
rs17006625 | snp | A/G | 0.0619247 | 0.164705 | missense, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20119604 | CCGGGGCAGTTATCA[A/G]TCCACCTCCTGTGGC | 8850 |
rs17006642 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KAT2B | GRCh38.p7 | 3:20141419 | TGGGGAGTACACAAA[A/G]GCCATTTATTGAAAG | 8850 |
rs17006645 | snp | A/C | 0.23846 | 0.249734 | intron-variant | KAT2B | GRCh38.p7 | 3:20141739 | TTTTTCTTTTACTTA[A/C]AGTGGCTCAGTCTTG | 8850 |
rs17006672 | snp | A/T | 0.0952156 | 0.196321 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20153353 | TGAGATTGAATCAAC[A/T]TGCTTTAATAGGAAA | 8850 |
rs17182383 | snp | C/T | 0.186105 | 0.241697 | intron-variant | KAT2B | GRCh38.p7 | 3:20073512 | GTAGATAATGTGATC[C/T]TCCCAAGAAGTCATC | 8850 |
rs17626938 | snp | A/G | 0.175576 | 0.238665 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20038640 | CAAGCTCTTATTAGT[A/G]TCTGTTAAATCCATG | 8850 |
rs17678713 | snp | A/G | 0.133777 | 0.221342 | intron-variant | KAT2B | GRCh38.p7 | 3:20151277 | GATGCTTTTGTGGTG[A/G]ATTTAGGATATTGAT | 8850 |
rs17796904 | snp | C/T | 0.110872 | 0.20771 | intron-variant | KAT2B | GRCh38.p7 | 3:20079857 | CAGCCTTTCAGATGC[C/T]GGTTTCAGAGTTTTC | 8850 |
rs17797193 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KAT2B | GRCh38.p7 | 3:20112832 | TGTTATTAGATTATG[A/G]AATTTTTGTCTCAGT | 8850 |
rs17797343 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | KAT2B | GRCh38.p7 | 3:20117701 | GAACTGTGGCTGTGT[G/T]GAAACGTAGATGAAC | 8850 |
rs17797581 | snp | C/T | 0.318896 | 0.240319 | intron-variant | KAT2B | GRCh38.p7 | 3:20132904 | CAACAATCTCTCTTG[C/T]ATCGACATCCGTGTT | 8850 |
rs28475027 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20108991 | CCTGGTGCCAAAAAA[A/G]TTGGGGACCTCTGCC | 8850 |
rs28477356 | snp | A/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20126531 | CTTAAAAAAAAAAAA[A/C]AAAAAACTAGGCCGG | 8850 |
rs28477581 | snp | A/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20126532 | TTAAAAAAAAAAAAC[A/C]AAAAACTAGGCCGGG | 8850 |
rs28495406 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KAT2B | GRCh38.p7 | 3:20096432 | GGTTGCCAAAAATAG[A/T]TCTATAAAGGAGGCT | 8850 |
rs28542078 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20078204 | TAAATAAATAAATAA[A/T]TAAAAAGGCAGCCTG | 8850 |
rs28563940 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20071018 | TGTATATAAAAAAAA[A/C]AAAACCAAAAAGTTT | 8850 |
rs28615631 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20106979 | TATATATATATATAT[A/G]TATATATATATATAT | 8850 |
rs28631147 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20130142 | GCCACCACGCCCGGC[C/T]TCAGCACGAATTATA | 8850 |
rs28642299 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20146788 | TAGATCATTTACTGT[A/T]AAAGGGCACATAGCC | 8850 |
rs28665161 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20103401 | ACATTAGTATATTTT[A/G]TTTTATTTTTATTTT | 8850 |
rs28695701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT2B | GRCh38.p7 | 3:20106892 | ATGCAAGCCAGATAT[A/G]TAATTAAAAATTTTC | 8850 |
rs28704852 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | KAT2B | GRCh38.p7 | 3:20149564 | AAGAGTGAAAGGGAC[A/C/G]CATTAGCTCCTTGAA | 8850 |
rs28716666 | snp | C/T | 0.208169 | 0.246476 | intron-variant | KAT2B | GRCh38.p7 | 3:20106917 | ATTTTCTAGTAGCTA[C/T]GTATAAAATGAATAG | 8850 |
rs33955642 | in-del | -/CTT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20139218 | TGCACCCAGCCAGAC[-/CTT]TTCTTTTTTTTTAAA | 8850 |
rs34023053 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20062449 | TAATATATAGAAATT[-/C]ATATATATTTTATTT | 8850 |
rs34061018 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20058454 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8850 |
rs34080581 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20060291 | ATGTTTAACTTTTTG[-/A]AAAAATTGTTGTTTC | 8850 |
rs34081141 | in-del | -/CTT | 0.433673 | 0.1696 | intron-variant | KAT2B | GRCh38.p7 | 3:20108279 | AAATTAAAAGTTAAA[-/CTT]CTCAGTCATACTAGC | 8850 |
rs34125166 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20091137 | AGGTCCTGGGCTTTT[-/A]CCATGATGGAAGATT | 8850 |
rs34159701 | snp | C/T | 0.151334 | 0.229706 | intron-variant | KAT2B | GRCh38.p7 | 3:20149037 | TTTTACGCTTTGTCT[C/T]ATATCCAAAATCAAA | 8850 |
rs34186642 | in-del | -/T/TT | 0.447291 | 0.153545 | intron-variant | KAT2B | GRCh38.p7 | 3:20141786 | GAAGTGAGCAAAGGC[-/T/TT]TTTTTTTTTTTTTTG | 8850 |
rs34204839 | snp | C/T | 0.187053 | 0.241946 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20071332 | CATCTGTGTTACATG[C/T]TATTCTAACAATGTA | 8850 |
rs34236820 | in-del | -/T | 0.138886 | 0.22395 | intron-variant | KAT2B | GRCh38.p7 | 3:20117100 | TCTGTGTGTGAAAAC[-/T]CCCCTTGACCCTTGT | 8850 |
rs34256349 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20078505 | GCCTCTCGAGTAGCT[-/G]GGGACCACAGACATG | 8850 |
rs34270654 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20075907 | CGAGACTCCCATCTC[-/A]AAAAAAAAAAAAAAA | 8850 |
rs34271857 | in-del | -/A | 0.476833 | 0.105105 | intron-variant | KAT2B | GRCh38.p7 | 3:20125306 | GAGACTCCGTCTCAG[-/A]AAAAAAAAAAAAAAA | 8850 |
rs34305027 | in-del | -/A | | | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20038924 | ACTGTTTAGATCTAC[-/A]AAACTCCCCCACCTC | 8850 |
rs34333062 | in-del | -/AG | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20096952 | AAAGAATAATAGGAA[-/AG]AGAGAGAGAGAGAGA | 8850 |
rs34386078 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20119278 | GCTGCCAAATAGTGA[-/T]TTTTTTTTTTTTTTT | 8850 |
rs34397287 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20152143 | TACATTTTTAAAAAA[-/C]CCCACAAAAGAATGA | 8850 |
rs34431414 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20126518 | GAAAATCCATTGCTT[-/A]AAAAAAAAAAAACAA | 8850 |
rs34515517 | snp | A/C | 0.181659 | 0.240478 | intron-variant | KAT2B | GRCh38.p7 | 3:20058998 | TCCTGAGTAGATTGG[A/C]GTTTGAGAAGCACTA | 8850 |
rs34527737 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20062434 | ATTATATATAATATA[-/C]TAATATATAGAAATT | 8850 |
rs34572705 | snp | C/G | 0.135484 | 0.22223 | intron-variant | KAT2B | GRCh38.p7 | 3:20090767 | TTTTTTAGAGTTTCA[C/G]TTTGTCATAAAGGCT | 8850 |
rs34589089 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20068141 | AGCTGGGATTACAGG[CA/TG]TGCACCACCATGCCG | 8850 |
rs34600923 | in-del | -/C | 0.184838 | 0.241358 | intron-variant | KAT2B | GRCh38.p7 | 3:20099047 | CACATGTAAAAGTTA[-/C]AGAAGATTCAAGCAA | 8850 |
rs34620777 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20055461 | TAAATGAGAATGCCT[-/G]GGGGAATTCCTCTAG | 8850 |
rs34735719 | in-del | -/T | 0.436692 | 0.166271 | intron-variant | KAT2B | GRCh38.p7 | 3:20114533 | ATAAATATTAGTAAC[-/T]TTTATGATGGTAATG | 8850 |
rs34777029 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20067807 | GCCTCCCAAGTAGCT[-/G]GGGATTACAGGTGCC | 8850 |
rs34786117 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20087750 | ACAAATAAGATCATG[-/C]CAGTATTTGTCTTTC | 8850 |
rs34796976 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20124625 | TGGAGGGGTCACACA[-/T]TTCAAACTACATCAG | 8850 |
rs34812840 | multinucleotide-polymorphism | CG/TA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20099451 | GCTTCAGCACACCTA[CG/TA]GTGGCCTGGATGGGC | 8850 |
rs35016483 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20087953 | CTAATTAAAAAAAAA[-/T]TTTTTTTTTGTAGAG | 8850 |
rs35017674 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20110706 | GAAAGAAAAAGAAAG[-/C]AAAAAGAGGTTTATT | 8850 |
rs35018157 | in-del | -/T | 0.227074 | 0.248947 | intron-variant | KAT2B | GRCh38.p7 | 3:20147095 | AGCCATTGAATATCA[-/T]TTGGCAATTTTGTTC | 8850 |
rs35102951 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20105800 | GCACGACCCTGTCTG[-/A]AAAAAAAAAAAAAAA | 8850 |
rs35132602 | in-del | -/A | 0.138886 | 0.22395 | intron-variant | KAT2B | GRCh38.p7 | 3:20090012 | AAAAAACAAAACAAG[-/A]AAAAAAAAAACGAAT | 8850 |
rs35182385 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20103806 | AAGTAGTAAAAATGG[-/A]AAATTGGTTTGGATG | 8850 |
rs35234629 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20047243 | TTTGTATTTTTTATA[-/G]GAGATGTTTCGCCAA | 8850 |
rs35239760 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20058454 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8850 |
rs35278480 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20044415 | AGCAAGATTCTCCCT[-/A]AAAAAAAAAAATAAA | 8850 |
rs35313843 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20124508 | CTCATTCATCAACAA[-/G]GGGGATGGTGCTAGG | 8850 |
rs35394514 | in-del | -/CACA | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20060620 | ACAAACAAACAAACA[-/CACA]AACAACAAACTGTGG | 8850 |
rs35396610 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20043429 | CAGAAAAACTACTTT[-/C]CTTGGAGTAGTTGCG | 8850 |
rs35424474 | snp | C/T | 0.22192 | 0.248418 | synonymous-codon, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20099864 | GATTTCTTTGCAGCT[C/T]TTGAGAAAGTCTATT | 8850 |
rs35446606 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20135759 | TGGCTTGGGACTGGG[-/A]AAAGTACGGATGGGC | 8850 |
rs35457765 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20047607 | CTTGCCGTGAGTACC[-/T]TTTTTTTTTTTTTTT | 8850 |
rs35482283 | snp | A/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20068255 | CCTGCCTCGGCCTCC[A/C]AAAGTGCTGCAATTA | 8850 |
rs35536387 | in-del | -/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20124115 | TTTCCATTTCCTTCC[-/T]AGATGTCCAGTCTGT | 8850 |
rs35537611 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20090827 | CAACCTCAATCTTGT[-/G]GGGGTGGGTTCAAGC | 8850 |
rs35545255 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20106439 | AACAACACCAGAAGT[-/A]CACACACACACACAC | 8850 |
rs35553228 | in-del | -/AG | 0.140242 | 0.224618 | intron-variant | KAT2B | GRCh38.p7 | 3:20142568 | GTAGTTGTCATTAGT[-/AG]AGAGAGAGAGAGAGA | 8850 |
rs35562268 | snp | G/T | 0.369346 | 0.219673 | intron-variant | KAT2B | GRCh38.p7 | 3:20084802 | AGCCTTCTAAAAATA[G/T]AAGCTTTCACCTCTA | 8850 |
rs35578668 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20104491 | GGGGAATTAAAAAAA[-/C]CCACATACCACCACA | 8850 |
rs35619895 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20124558 | CTGATGATCCAACAC[-/T]TTCCCACTAGGCCCC | 8850 |
rs35626881 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20124111 | GATCTTTCCATTTCC[-/T]TCCTAGATGTCCAGT | 8850 |
rs35630745 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20089943 | CCAGAATTTGAGAAG[-/A]AACAGCTTGGGCAAC | 8850 |
rs35632245 | snp | A/G | 0.182933 | 0.240836 | intron-variant | KAT2B | GRCh38.p7 | 3:20052865 | CCTGTAATCCCAGCT[A/G]TTCGGGAGGCTGAGG | 8850 |
rs35638647 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20046378 | TTGAGCTCACGAGTT[-/C]CGAGACCAGCCTGGG | 8850 |
rs35645247 | snp | C/G | 0.138886 | 0.22395 | intron-variant | KAT2B | GRCh38.p7 | 3:20094537 | GTAATAACCTTAAAA[C/G]ATGGACTGTATTTGA | 8850 |
rs35659955 | snp | A/G | 0.183568 | 0.241012 | intron-variant | KAT2B | GRCh38.p7 | 3:20052121 | GCCATGTATCTCTGT[A/G]TCTTGTTCTCAAAGC | 8850 |
rs35736178 | in-del | -/A | 0.499908 | 0.00678851 | intron-variant | KAT2B | GRCh38.p7 | 3:20097527 | ACAAAAATAATGATT[-/A]AAATTTTTTTTTAAT | 8850 |
rs35771269 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20127253 | AGGCGACCTAGCTCT[-/A]AAAAGTTCAGATAAA | 8850 |
rs35776229 | snp | A/G | 0.18134 | 0.240387 | intron-variant | KAT2B | GRCh38.p7 | 3:20059920 | CCACCCCAGATGACC[A/G]CTAATCTTTCTGTCT | 8850 |
rs35801709 | snp | A/G | 0.467946 | 0.122472 | intron-variant | KAT2B | GRCh38.p7 | 3:20125447 | GGCAAACTATAACCC[A/G]CAGGCCACATTTTGT | 8850 |
rs35808397 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20053096 | TAGTTAAGTGTGTTT[-/C]CCCTTGGTTCATGGC | 8850 |
rs35815952 | snp | C/G | 0.387832 | 0.208572 | intron-variant | KAT2B | GRCh38.p7 | 3:20054362 | TTGAATTCCTGACCT[C/G]GTGATCCACCCTCAT | 8850 |
rs35821826 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20089966 | GGGCAACATAGTGAG[-/A]AAGCCATCTCTATTA | 8850 |
rs35825025 | in-del | -/T/TT/TTT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20047606 | CTTGCCGTGAGTACC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 8850 |
rs35841175 | snp | C/T | 0.142609 | 0.225759 | intron-variant | KAT2B | GRCh38.p7 | 3:20123150 | GTTAACATTATGCCA[C/T]ATTTGCTACCTCTCT | 8850 |
rs35885737 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20098196 | ATCATGCCACTGCAC[-/T]TCCAACCTGGCCGAC | 8850 |
rs35891853 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20053917 | TTCTCCTGCCTCAGT[-/G]CTCCCAAGTAGCTGA | 8850 |
rs35895255 | snp | A/T | 0.386694 | 0.20932 | intron-variant | KAT2B | GRCh38.p7 | 3:20146671 | AATATCCACCACTTA[A/T]TGAGTCTGCCATTTG | 8850 |
rs35915124 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20068251 | CCGCCTGCCTCGGCC[-/T]TCCCAAAGTGCTGCA | 8850 |
rs36029475 | snp | A/G | 0.140919 | 0.224948 | intron-variant | KAT2B | GRCh38.p7 | 3:20114112 | TTTTATTCTTTTTAA[A/G]TCACCTGCCCTATTC | 8850 |
rs36058009 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20063534 | TTCTGAGTAGGCCTC[-/T]TTTTTTTTTTTTTTT | 8850 |
rs36059306 | in-del | -/G | 0.173643 | 0.238054 | intron-variant | KAT2B | GRCh38.p7 | 3:20044589 | TCCTTTCACCTAGTC[-/G]GGGGTGAGGTGGGGT | 8850 |
rs36093749 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20130940 | CGTGTGTGTGTGTGT[G/T]CTAATGGTAAGAACC | 8850 |
rs41276509 | snp | A/G | 0.393987 | 0.204372 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20152763 | ACTACTATTAAGGTA[A/G]ATTTTCTATGGCATG | 8850 |
rs41285055 | snp | A/G/T | 0.00913058 | 0.0669488 | intron-variant | KAT2B | GRCh38.p7 | 3:20072287 | AAACCATCAGTCCAC[A/G/T]GCTGCCTGTTAAATA | 8850 |
rs41285057 | snp | C/G | 0.208188 | 0.246479 | intron-variant | KAT2B | GRCh38.p7 | 3:20099773 | TAAGAGAGAGAGAGA[C/G]AGACAGACAGAAACA | 8850 |
rs41285059 | snp | A/G | 0.000567452 | 0.0168346 | missense, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20122790 | ACGGACCCTGCAGCA[A/G]TGCTTGGACCAGAGG | 8850 |
rs41285061 | snp | C/G | 0.21992 | 0.248184 | intron-variant | KAT2B | GRCh38.p7 | 3:20127383 | AGTATATTTATATAA[C/G]TAGGATAGGTAAAAC | 8850 |
rs55653348 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20110673 | TGAGACCCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 8850 |
rs55729941 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | KAT2B | GRCh38.p7 | 3:20068537 | CCTGTACTCATCCTT[C/T]TTTCTTTCTTTCCAT | 8850 |
rs55783650 | snp | A/G | 0.40595 | 0.195396 | intron-variant | KAT2B | GRCh38.p7 | 3:20122163 | CTTACTGATATCCAT[A/G]CAACATGATCTGTAA | 8850 |
rs55828442 | snp | C/T | 0.444444 | 0.157135 | intron-variant | KAT2B | GRCh38.p7 | 3:20144286 | GGATTCTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 8850 |
rs55845090 | in-del | -/GC/GT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20142904 | TGTGTGTGTGTGTGT[-/GC/GT]ACGTACATATACCTA | 8850 |
rs55977517 | in-del | -/TCT | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20108281 | ATTAAAAGTTAAACT[-/TCT]CAGTCATACTAGCCA | 8850 |
rs56042248 | snp | C/T | 0.208169 | 0.246476 | intron-variant | KAT2B | GRCh38.p7 | 3:20102133 | CCAGCCTGGCCAATA[C/T]GGTGAAACCCCATCT | 8850 |
rs56067451 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20149493 | GGAGGGAGACCGTAT[C/T]TCAAAAAAAAAAAAA | 8850 |
rs56091316 | in-del | -/A | | | intron-variant | KAT2B | GRCh38.p7 | 3:20149520 | AAAAAAAAAAAAAAA[-/A]TTGTGGAAGTGTTAA | 8850 |
rs56103847 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | KAT2B | GRCh38.p7 | 3:20081804 | TCATGAGAATAATAA[C/T]GAAGAATATCCCATA | 8850 |
rs56117426 | snp | C/T | 0.161267 | 0.233723 | intron-variant | KAT2B | GRCh38.p7 | 3:20052744 | AGGCTGAGGTGGTCA[C/T]ATCACCTGAGGTCGG | 8850 |
rs56239971 | in-del | -/ATTTATTATTTATTT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20092246 | TTTATTTATTTATTT[-/ATTTATTATTTATTT]GAGATGGAGTGTTGC | 8850 |
rs56337237 | snp | G/T | 0.079617 | 0.182947 | intron-variant | KAT2B | GRCh38.p7 | 3:20083679 | GCTATTTTATTATAG[G/T]AGGTTTGACATTCCA | 8850 |
rs56729913 | snp | A/T | 0.496175 | 0.0435625 | intron-variant | KAT2B | GRCh38.p7 | 3:20143361 | AGTCAGAATGGCTAT[A/T]ATTAAGAAGTTAAAA | 8850 |
rs56768621 | snp | A/G | 0.329084 | 0.237162 | intron-variant | KAT2B | GRCh38.p7 | 3:20051491 | TCGGTGAGCCATGCA[A/G]AACCATACATGTTGA | 8850 |
rs56780132 | in-del | -/A | 0.461592 | 0.133149 | intron-variant | KAT2B | GRCh38.p7 | 3:20141370 | AATTTTCTAAGGCAG[-/A]AAAAAAAAACACTCA | 8850 |
rs56900166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20058861 | AAACCATCTTTATCT[C/T]TTCAAATCTTGGCTA | 8850 |
rs56911455 | in-del | -/CAAAATATGTAAAATA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20140897 | AAAATATGTAAAATA[-/CAAAATATGTAAAATA]TGGTGACATATTTTA | 8850 |
rs56930557 | snp | A/T | 0.29309 | 0.246258 | intron-variant | KAT2B | GRCh38.p7 | 3:20146672 | ATATCCACCACTTAA[A/T]GAGTCTGCCATTTGT | 8850 |
rs57008249 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | KAT2B | GRCh38.p7 | 3:20146712 | CGAATTATTACACAT[A/G]TGCAACCTTGAAAGC | 8850 |
rs57121762 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20150006 | GCGATAGGTCTAGCA[A/G]ATCTCGTCGATCATA | 8850 |
rs57379127 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KAT2B | GRCh38.p7 | 3:20127978 | TCGTGCTGTGCAGCC[A/C]GGTCCCTAACAGGCC | 8850 |
rs57415080 | in-del | -/CA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20106464 | ACACACACACACACA[-/CA]TTCTGTCTCTCTCAC | 8850 |
rs57566579 | snp | C/T | 0.187053 | 0.241946 | intron-variant | KAT2B | GRCh38.p7 | 3:20139246 | AAAAATGTGTTCTTA[C/T]GTAATTAGAAAGCTT | 8850 |
rs57662568 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20151453 | TGGGGTTTTTTTTTT[-/T]CCCATTTGACTTATT | 8850 |
rs57842862 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KAT2B | GRCh38.p7 | 3:20083475 | TTAGAGTGAGGTTCA[C/T]CTGGGTGTTGACATG | 8850 |
rs57934862 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20112180 | GCTTTTTTTTTTTTT[-/T]CCGTTCAATTTCTCC | 8850 |
rs58066806 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20101170 | AGGAAGAGATTTTTG[G/T]GAATAGAGAAATGTC | 8850 |
rs58182310 | in-del | -/T/TT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20139071 | CAATTTTTTTTTTTT[-/T/TT]AATCATTTGTAGAGA | 8850 |
rs58218798 | snp | C/T | 0.207253 | 0.246318 | intron-variant | KAT2B | GRCh38.p7 | 3:20130258 | AATTCAGCAGTCTTA[C/T]ATTCATCATTCTGAC | 8850 |
rs58430200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20128197 | ATGAAGGGATATTTG[A/G]AAAATAGATCTCAGT | 8850 |
rs58629324 | snp | C/T | 0.288386 | 0.247035 | intron-variant | KAT2B | GRCh38.p7 | 3:20102317 | CTCAAAAAAAAAATT[C/T]TTTTTAAAGGAAAGA | 8850 |
rs58815539 | in-del | -/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20063564 | TTTTTTTTTTTTTTT[-/T]GAGATGGTTGCTCTG | 8850 |
rs58969372 | snp | A/G | 0.122758 | 0.215196 | intron-variant | KAT2B | GRCh38.p7 | 3:20148889 | TTTGAATAATTATTC[A/G]GGATAATAATGAAAG | 8850 |
rs59044146 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | KAT2B | GRCh38.p7 | 3:20113773 | AGATGTGTTTTCAGG[C/G]CTTACATTCTTATCT | 8850 |
rs59165062 | snp | A/G | 0.078151 | 0.181571 | intron-variant | KAT2B | GRCh38.p7 | 3:20074555 | GATGTTGTTCGTAGT[A/G]GTGGTACTATAACAC | 8850 |
rs59200822 | snp | C/T | 0.168785 | 0.236441 | intron-variant | KAT2B | GRCh38.p7 | 3:20082116 | CTTGGCTTACTGCAG[C/T]CTCCACCTCCTGGGT | 8850 |
rs59213344 | snp | G/T | 0.0663309 | 0.169604 | intron-variant | KAT2B | GRCh38.p7 | 3:20130139 | TGAGCCACCACGCCC[G/T]GCCTCAGCACGAATT | 8850 |
rs59242139 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KAT2B | GRCh38.p7 | 3:20128045 | TCTCACTGTGAGTGT[A/T]TGTGTATGTGTGTGA | 8850 |
rs59256081 | snp | A/G | 0.188631 | 0.242351 | intron-variant | KAT2B | GRCh38.p7 | 3:20135286 | TTTACTAGACATACC[A/G]TCCCCTTATTATTAT | 8850 |
rs59374480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT2B | GRCh38.p7 | 3:20150255 | TTGTTCAGATGCTGA[A/G]TAAAATATTTAGTCT | 8850 |
rs59387877 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20105798 | AGAGCACGACCCTGT[C/T]TGAAAAAAAAAAAAA | 8850 |
rs59412430 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20063597 | GCCCAGGCTGGAATG[G/T]AGTGGCACAATCTCA | 8850 |
rs59501381 | in-del | -/TTTA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20138402 | ATACATTTTTGACTA[-/TTTA]GGTGTTTCTTGTAGG | 8850 |
rs59693808 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20087961 | AAAAAATTTTTTTTT[-/T]GTAGAGACAGGGTCT | 8850 |
rs59725039 | snp | A/G | 0.24449 | 0.249939 | intron-variant | KAT2B | GRCh38.p7 | 3:20052323 | TTTCCTTATGACAAT[A/G]GAAGCTCCATGAAGC | 8850 |
rs59957683 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20142769 | AGGCTCAGAGTCCAA[A/T]GGAAACAGATTTGTG | 8850 |
rs60106394 | snp | C/T | 0.207559 | 0.246371 | intron-variant | KAT2B | GRCh38.p7 | 3:20133567 | TTATGTAATCATTTC[C/T]CTATTGAAGACATAT | 8850 |
rs60294437 | snp | A/G | 0.131038 | 0.219882 | intron-variant | KAT2B | GRCh38.p7 | 3:20074253 | AACCTAAATATTCCA[A/G]TGTAGGAGATGATTG | 8850 |
rs60355368 | snp | A/T | 0.0948562 | 0.196037 | intron-variant | KAT2B | GRCh38.p7 | 3:20073121 | ATGATTAAAATATTT[A/T]AAAAAATCATGTGTT | 8850 |
rs60469487 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20062411 | ATTATATATTATATA[A/T]TATATATTATTATAT | 8850 |
rs60509027 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20133744 | CCCAGTTTACATTTT[-/T]CACCAGTGGTGTTGG | 8850 |
rs60596776 | snp | A/G | 0.33303 | 0.235809 | intron-variant | KAT2B | GRCh38.p7 | 3:20090615 | CTGTTGTGTATTTTT[A/G]CATCCATGTTCATCA | 8850 |
rs60601452 | in-del | -/A | 0.314544 | 0.241524 | intron-variant | KAT2B | GRCh38.p7 | 3:20074092 | GAATGAAAAAAAAAA[-/A]TCACATATCCTTTGA | 8850 |
rs60656536 | in-del | -/ATATATATATATATAT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20106963 | CTGAATTTTATGTGT[-/ATATATATATATATAT]GTATATATATATATA | 8850 |
rs60728324 | in-del | -/C/T | 1.77688e-05 | 0.00298062 | intron-variant | KAT2B | GRCh38.p7 | 3:20148047 | GTGATTTTTTTTTTT[-/C/T]CCCCACCAAGCAACT | 8850 |
rs60864750 | in-del | -/T | 0.442385 | 0.15965 | intron-variant | KAT2B | GRCh38.p7 | 3:20104891 | TTTGTTGTTTTTTTG[-/T]TTTTTTTTTTTTTGA | 8850 |
rs60916747 | snp | G/T | 0.17461 | 0.238362 | intron-variant | KAT2B | GRCh38.p7 | 3:20082402 | ATTAATATAATACCT[G/T]TATCTAATCTACTGT | 8850 |
rs60944875 | in-del | -/TG/TGTG | | | intron-variant | KAT2B | GRCh38.p7 | 3:20130871 | GTGTGTGTGTGTGTG[-/TG/TGTG]CGTGCATGTGTGTGT | 8850 |
rs60958319 | in-del | -/TT | 0.490508 | 0.0682328 | intron-variant | KAT2B | GRCh38.p7 | 3:20089417 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTCAC | 8850 |
rs61105111 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20074865 | TTTAACTCTGAAGTT[-/T]ACCCCAAGGGAACTA | 8850 |
rs61138004 | snp | C/G | 0.160609 | 0.233472 | intron-variant | KAT2B | GRCh38.p7 | 3:20104363 | GATGACACCAACCTC[C/G]CCCACGTCCCCACCA | 8850 |
rs61279125 | in-del | -/A/AAA | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20051199 | AAAAAAAAAAAAAAA[-/A/AAA]CCCAAACAAAAAAAA | 8850 |
rs61280687 | snp | A/G | 0.145642 | 0.227177 | intron-variant | KAT2B | GRCh38.p7 | 3:20149531 | AAAAATTGTGGAAGT[A/G]TTAAAAATGTGAAAA | 8850 |
rs61346536 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KAT2B | GRCh38.p7 | 3:20078676 | CGCACCCTTCATCAT[C/T]TTTTTCTGATATATG | 8850 |
rs61355879 | in-del | -/GAGA | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20096969 | AGAGAGAGAGAGAGA[-/GAGA]AAGAGAGTGGGGGAA | 8850 |
rs61440199 | snp | A/G | 0.186105 | 0.241697 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070054 | TGGGGGTAAGAGTTG[A/G]GCCTTCCTGATGCCT | 8850 |
rs61457790 | snp | A/G | 0.178785 | 0.239642 | intron-variant | KAT2B | GRCh38.p7 | 3:20094694 | AAGCTAAAATAGGCC[A/G]TGGGGACTTTGCAGC | 8850 |
rs61697250 | in-del | -/TT | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20079221 | TTTTTTTTTTTTTTT[-/TT]GCCACAGAGTCTGGC | 8850 |
rs62241663 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KAT2B | GRCh38.p7 | 3:20127826 | CATTAGTTAGATTCT[C/T]ATAAGGAGCATGCAA | 8850 |
rs62241664 | snp | C/T | 0.325327 | 0.238382 | intron-variant | KAT2B | GRCh38.p7 | 3:20129594 | TTGGCCAGGCTGGTC[C/T]TGAACTCCTGACCTC | 8850 |
rs62241665 | snp | C/T | 0.337841 | 0.23406 | intron-variant | KAT2B | GRCh38.p7 | 3:20134934 | AATAAGTATAAAATG[C/T]TAGTAATGAGAATTT | 8850 |
rs62241668 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20148051 | ATTTTTTTTTTTCCC[C/T]ACCAAGCAACTTAAA | 8850 |
rs62241669 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | KAT2B | GRCh38.p7 | 3:20149929 | TTGGGAAACCCCCAT[A/G]GGAAGCTGTGTGACT | 8850 |
rs62241670 | snp | A/G | | | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154904 | AAAAAAAAAAAAAAG[A/G]CATATGATGGCCAAA | 8850 |
rs62243072 | snp | C/T | 0.0414363 | 0.137845 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20038932 | AGATCTACAAACTCC[C/T]CCACCTCCCAATGTT | 8850 |
rs62243073 | snp | C/T | 0.41023 | 0.191902 | intron-variant | KAT2B | GRCh38.p7 | 3:20041783 | TCTTCCTGCCTGCTG[C/T]AAAGAGGGTCAAGTT | 8850 |
rs62243074 | snp | C/G | 0.137527 | 0.223271 | intron-variant | KAT2B | GRCh38.p7 | 3:20042638 | CTCAGTGTTTCTGTT[C/G]TGGCTTTATTTTAAA | 8850 |
rs62243075 | snp | C/G | 0.136506 | 0.222754 | intron-variant | KAT2B | GRCh38.p7 | 3:20045828 | AAAGGAATGATGTTA[C/G]CCGCCTCATGGCATA | 8850 |
rs62243076 | snp | C/T | 0.171704 | 0.237423 | intron-variant | KAT2B | GRCh38.p7 | 3:20046452 | CCGGGCATGATGGTG[C/T]GTGCCTGTAGTCCCT | 8850 |
rs62243080 | snp | C/T | 0.161267 | 0.233723 | intron-variant | KAT2B | GRCh38.p7 | 3:20052934 | TGAGCTGAGATTGCG[C/T]CACTGCACTCCAGCC | 8850 |
rs62243081 | snp | A/G | 0.15665 | 0.231917 | intron-variant | KAT2B | GRCh38.p7 | 3:20053383 | TCTATAAAAATACAA[A/G]AATTAGCTGGGCATG | 8850 |
rs62243098 | snp | A/C | 0.152334 | 0.230133 | intron-variant | KAT2B | GRCh38.p7 | 3:20066662 | CACCTCGGCATCCCA[A/C]AGTGCTGGGATTACA | 8850 |
rs62243099 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20071304 | TGTAGATGGCTCTAC[C/T]CTAGAGTGACTTCAT | 8850 |
rs62243100 | snp | A/G | 0.158962 | 0.232835 | intron-variant | KAT2B | GRCh38.p7 | 3:20079161 | CCGCCTCGGCCTCTC[A/G]AAGTGCTGGGATTAC | 8850 |
rs62243129 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20085196 | CTCTATGTCTATTAA[A/T]TTAAAAAAAAAGTTT | 8850 |
rs62243131 | snp | A/G | 0.304021 | 0.244131 | intron-variant | KAT2B | GRCh38.p7 | 3:20099816 | GAGAGAGATAGACAT[A/G]CCAATTAAGTTTTTC | 8850 |
rs62243133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20105583 | GGAGTTTGAGCCCAG[C/T]CTGGGCAACAGAATG | 8850 |
rs62243134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20105584 | GAGTTTGAGCCCAGC[C/T]TGGGCAACAGAATGA | 8850 |
rs62243135 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20116335 | ACTCTTCCCTAAGTT[C/T]TCCCATCCCCTCTAG | 8850 |
rs62243136 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20120338 | GTTTAAGTGACTCTC[C/T]TGCCTCAGTCTCCTG | 8850 |
rs62243138 | snp | A/G | 0.34146 | 0.23267 | intron-variant | KAT2B | GRCh38.p7 | 3:20123379 | ACAATATTTTCTAAT[A/G]CAGGGTTGGTGAATT | 8850 |
rs66582607 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20133430 | TACATGTGACTAATA[-/C]TTACCATATTGGATA | 8850 |
rs66606824 | in-del | -/A/AGA | 0.5 | 0 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070323 | GCGAGACTCCATCTC[-/A/AGA]AAAAAAAAAAAAAAG | 8850 |
rs66736930 | in-del | -/T | 0.138886 | 0.22395 | intron-variant | KAT2B | GRCh38.p7 | 3:20089364 | TGATAAGATATCTTT[-/T]ATGTTCACAGATTGG | 8850 |
rs66950718 | in-del | -/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20065313 | TGCACTCCCTAAAAG[-/G]TTGTCCTTCAGCTGG | 8850 |
rs67432468 | in-del | -/A | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20125325 | AAAAAAAAAAAAAAA[-/A]GAATATATACATGAG | 8850 |
rs67660889 | snp | C/G | 0.163564 | 0.234582 | intron-variant | KAT2B | GRCh38.p7 | 3:20129046 | AATGTTATTCATTTA[C/G]GATTTTCATGGGTGG | 8850 |
rs67713322 | snp | G/T | 0.25801 | 0.249872 | intron-variant | KAT2B | GRCh38.p7 | 3:20106766 | ATCATCTTTGTATCA[G/T]AAATAATGTCAGTCT | 8850 |
rs67857568 | in-del | -/ACAG | | | intron-variant | KAT2B | GRCh38.p7 | 3:20106453 | ACACACACACACACA[-/ACAG]CACACACACACATTC | 8850 |
rs68050031 | snp | C/T | 0.222333 | 0.248464 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20153903 | GCCAGTGATAATCTG[C/T]ATGAAGGAAAAAGAA | 8850 |
rs68118391 | in-del | -/GAA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20113945 | TTCAGGGAAAAAATG[-/GAA]AAGAAGACCACTGAT | 8850 |
rs71038668 | in-del | -/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20107542 | GCCTCCCAAGTAGCT[-/G]GGGATTACAGGTGCC | 8850 |
rs71038669 | in-del | -/C | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20118748 | TAGTTCGCTCTCTCT[-/C]TTTTTTTTTTTTTTT | 8850 |
rs71266472 | in-del | -/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20126530 | CGGCCTAGTTTTTTG[-/T]TTTTTTTTTTTTAAG | 8850 |
rs71266473 | in-del | -/A | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20119296 | GTTATGGTAGTTAGT[-/A]AAAAAAAAAAAAAAA | 8850 |
rs71316245 | snp | A/G | 0.499382 | 0.017561 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070520 | CATGTTAGCCAGGGT[A/G]ATCTCGATCTCCTGA | 8850 |
rs71316246 | snp | C/G | 0.138546 | 0.223781 | intron-variant | KAT2B | GRCh38.p7 | 3:20088119 | GTATTTGATTGTGTT[C/G]ATATACTACATTCTC | 8850 |
rs71316247 | snp | A/T | 0.133435 | 0.221162 | intron-variant | KAT2B | GRCh38.p7 | 3:20090609 | GGTTTTCTGTTGTGT[A/T]TTTTTGCATCCATGT | 8850 |
rs71316248 | snp | A/G | 0.138886 | 0.22395 | intron-variant | KAT2B | GRCh38.p7 | 3:20097240 | TACCCTGTTGGAAGT[A/G]AAGGTGGTGTCAAGG | 8850 |
rs71316249 | snp | A/G | 0.140242 | 0.224618 | intron-variant | KAT2B | GRCh38.p7 | 3:20108868 | GGATCTAAGCTGTAC[A/G]TTCTTTCTGAGAGTC | 8850 |
rs71624359 | multinucleotide-polymorphism | AGG/GGA | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20124113 | ACAGACTGGACATCT[AGG/GGA]AGGAAATGGAAAGAT | 8850 |
rs71634893 | in-del | -/ACAC | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20060619 | AACAAACAAACAAAC[-/ACAC]AAACAACAAACTGTG | 8850 |
rs71634894 | in-del | -/TTATA | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20061838 | ATAATATATAATATA[-/TTATA]CATAAAATATATATA | 8850 |
rs71634896 | in-del | -/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20077902 | GCTTGGGTCTTGCAT[-/G]GGTGGCTCACACCTG | 8850 |
rs71634897 | in-del | -/CA/CACA | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20106465 | ACACACACACACACA[-/CA/CACA]TTCTGTCTCTCTCAC | 8850 |
rs71809828 | in-del | -/CTT/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20108280 | AATTAAAAGTTAAAC[-/CTT/T]TCAGTCATACTAGCC | 8850 |
rs71853298 | in-del | -/TTTTC | 0.5 | 0 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20069520 | GCAGAGAGCTTTTCT[-/TTTTC]TTTTCTTTTCTTTTC | 8850 |
rs71925768 | in-del | -/T | 0.464309 | 0.12873 | intron-variant | KAT2B | GRCh38.p7 | 3:20144208 | TGAAGAGAAGGAAAC[-/T]TTTCAAATTGAAACA | 8850 |
rs71937317 | in-del | -/GGCTGGAGTGCAGTGGCGCAGTCTC | | | intron-variant | KAT2B | GRCh38.p7 | 3:20086826 | GATGGAGTCTCGCAG[-/GGCTGGAGTGCAGTGGCGCAGTCTC]GCTGGAGTGCAGTGG | 8850 |
rs72060525 | in-del | -/TGTAAAATACAAAATA | 0.451732 | 0.147663 | intron-variant | KAT2B | GRCh38.p7 | 3:20140872 | TACTTTTTAAATTTG[-/TGTAAAATACAAAATA]TGTAAAATACAAAAT | 8850 |
rs72097262 | in-del | -/AAT | 0.030278 | 0.119257 | intron-variant | KAT2B | GRCh38.p7 | 3:20149345 | CTACAAAAAGTAAAA[-/AAT]TAGCCAGGTGCAGTG | 8850 |
rs72120274 | in-del | -/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20147367 | TTTTGTTTTTTTTTT[-/T]GTACATTAACTACTC | 8850 |
rs72272809 | in-del | -/TATT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20138401 | AATACATTTTTGACT[-/TATT]AGGTGTTTCTTGTAG | 8850 |
rs72337393 | in-del | -/GT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20130861 | TGAGTTTAGTGTGTG[-/GT]TGTGTGTGTGCGTGC | 8850 |
rs72571858 | in-del | -/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20133428 | GCTACATGTGACTAA[-/C]TMWTACCATATTGGA | 8850 |
rs72571860 | in-del | -/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20150889 | CCCCCTTTTKGGGGG[-/G]GTACATGTTTCTTCC | 8850 |
rs73034177 | snp | G/T | 0.181978 | 0.240568 | intron-variant | KAT2B | GRCh38.p7 | 3:20044610 | GAGGTGGGGTGAGGG[G/T]CTTTGCACATGCTGT | 8850 |
rs73038113 | snp | A/T | 0.159622 | 0.233092 | intron-variant | KAT2B | GRCh38.p7 | 3:20097533 | ATAATGATTAAAATT[A/T]TTTTTTAATTTTAAC | 8850 |
rs73177838 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | KAT2B | GRCh38.p7 | 3:20042467 | CATACTGCTTGGGTG[A/G]TGACTACACCAAAAT | 8850 |
rs73179712 | snp | A/G | 0.394904 | 0.203722 | intron-variant | KAT2B | GRCh38.p7 | 3:20049221 | AGGAGTCCAGGTGCC[A/G]CCTCATTGACTTATT | 8850 |
rs73179716 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | KAT2B | GRCh38.p7 | 3:20052053 | TTGAATCACATTCAT[C/T]TCTAGCATCTAATTG | 8850 |
rs73179742 | snp | C/T | 0.029116 | 0.117091 | intron-variant | KAT2B | GRCh38.p7 | 3:20063202 | CCTTCTGAGTGGCTG[C/T]GACTGCAGGCGTGCA | 8850 |
rs73179773 | snp | C/T | 0.461592 | 0.133149 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070742 | TGCTGGTCACGGTGG[C/T]GCACGCCTGTAATAC | 8850 |
rs73181606 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KAT2B | GRCh38.p7 | 3:20075861 | AGGCTGCAGTGAGCC[A/G]AGATCTCACCACTGC | 8850 |
rs73181611 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | KAT2B | GRCh38.p7 | 3:20080769 | GTGAAATGCACACAG[C/G]TTTTGAAGACTTAGT | 8850 |
rs73818808 | snp | C/T | 0.178144 | 0.239451 | intron-variant | KAT2B | GRCh38.p7 | 3:20094593 | TGAGGAGAGAGTCAA[C/T]GGACAGGTCACAAAA | 8850 |
rs73818810 | snp | C/T | 0.178144 | 0.239451 | intron-variant | KAT2B | GRCh38.p7 | 3:20101888 | ATTCCAGTGTGGCTA[C/T]TAGAAAATTTAAAAT | 8850 |
rs73818811 | snp | A/G | 0.177824 | 0.239355 | intron-variant | KAT2B | GRCh38.p7 | 3:20103223 | AATAAGAGTTGAGAC[A/G]ATAAGTCTCTCAAAA | 8850 |
rs73818812 | snp | C/T | 0.127944 | 0.218179 | intron-variant | KAT2B | GRCh38.p7 | 3:20105993 | AGCATGGAAAGAACA[C/T]TAGGAAACAGGAGAT | 8850 |
rs73818813 | snp | C/T | 0.177503 | 0.239258 | intron-variant | KAT2B | GRCh38.p7 | 3:20106593 | AGTATAAATTGAGGT[C/T]TATAAAATGACTTTG | 8850 |
rs73818815 | snp | A/T | 0.177503 | 0.239258 | intron-variant | KAT2B | GRCh38.p7 | 3:20106595 | TATAAATTGAGGTCT[A/T]TAAAATGACTTTGAG | 8850 |
rs73818816 | snp | C/G | 0.200801 | 0.245111 | intron-variant | KAT2B | GRCh38.p7 | 3:20106824 | CCTCAGATGGAAATG[C/G]TGTTTAGACTCTAAA | 8850 |
rs73818820 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | KAT2B | GRCh38.p7 | 3:20121673 | AAAAATAATTTATGG[C/T]ATATTTCAAATATAT | 8850 |
rs73818821 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | KAT2B | GRCh38.p7 | 3:20121985 | AATAAAGCCCAAAGC[C/T]TAATGCAAACTGATT | 8850 |
rs73818824 | snp | C/T | 0.136506 | 0.222754 | intron-variant | KAT2B | GRCh38.p7 | 3:20133823 | AACGTATTTGCACGC[C/T]GTCAAGTGCAATATT | 8850 |
rs73818840 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20139224 | CCAGCCAGACTTCTT[C/T]TTTTTTAAAAATGTG | 8850 |
rs73819092 | snp | A/G | 0.164546 | 0.234942 | intron-variant | KAT2B | GRCh38.p7 | 3:20051381 | TCTCCCCTGGAGTCC[A/G]TATTGGTGAGTCCTT | 8850 |
rs73819096 | snp | A/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20064694 | CTTTCTCTTTTAATA[A/G]TGGCAATAATTCATA | 8850 |
rs73822403 | snp | A/T | 0.17138 | 0.237316 | intron-variant | KAT2B | GRCh38.p7 | 3:20081367 | CAGTGTGCTTCCTGT[A/T]CTCAGCAAGGTTGAC | 8850 |
rs74327932 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | KAT2B | GRCh38.p7 | 3:20043729 | AGATTTGCTTTTTTT[A/T]AAAAAAAAAAAAATT | 8850 |
rs74357757 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KAT2B | GRCh38.p7 | 3:20099266 | GAAATGAAAAAAAGA[C/G]TGTAACAGTGAAAGT | 8850 |
rs74370256 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20140897 | AAAATATGTAAAATA[C/T]AAAATATGTAAAATA | 8850 |
rs74410173 | snp | C/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20090950 | AGAAACAGGGTCTCA[C/G]TATGTTGTGCAGGCT | 8850 |
rs74414301 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KAT2B | GRCh38.p7 | 3:20051469 | CTAGAGTTGCTATAC[A/G]TTGTAGTCGGTGAGC | 8850 |
rs74416814 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | KAT2B | GRCh38.p7 | 3:20075550 | TTGCTTCTGACCTAC[C/T]GGCTATAAATCAGGG | 8850 |
rs74461468 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KAT2B | GRCh38.p7 | 3:20117388 | TAATTAGCATGTCTG[C/T]GTATCGATGCAACTG | 8850 |
rs74481136 | snp | A/C | 0.0592355 | 0.161582 | intron-variant | KAT2B | GRCh38.p7 | 3:20049773 | CTCTTGATTGTTTTA[A/C]AGTTGACAATCAAGA | 8850 |
rs74491806 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KAT2B | GRCh38.p7 | 3:20056007 | ATTCTGCTGTATGGA[C/T]GTACTAGTTTGTTTA | 8850 |
rs74555148 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KAT2B | GRCh38.p7 | 3:20066281 | TTTCTCTTAGGAAAA[C/T]GCCAGTCATTGGTTT | 8850 |
rs74556792 | snp | C/G | 0.136506 | 0.222754 | intron-variant | KAT2B | GRCh38.p7 | 3:20118401 | CTTAGGGGAAGAGTA[C/G]AGAGAGAGAAAAAAA | 8850 |
rs74667469 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KAT2B | GRCh38.p7 | 3:20079612 | ATTTTTCTCATGGAT[A/G]TTTCAAGTATTTAAA | 8850 |
rs74713463 | snp | A/C/G | 0.167158 | 0.235875 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20039998 | AGCGGTAGGTGTCGA[A/C/G]GCACTGGGGTGGGGG | 8850 |
rs74735294 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KAT2B | GRCh38.p7 | 3:20124115 | CTTTCCATTTCCTCC[C/T]AGATGTCCAGTCTGT | 8850 |
rs74743651 | snp | G/T | 0.234109 | 0.249494 | intron-variant | KAT2B | GRCh38.p7 | 3:20113501 | TTCTGGCATGCTTAT[G/T]CTAGGAGCTAAAACA | 8850 |
rs74796696 | snp | C/G/T | 0.5 | 0 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20039242 | CCACAGTCATCAACA[C/G/T]TGAAAACAACAGTTT | 8850 |
rs74808282 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | KAT2B | GRCh38.p7 | 3:20125773 | TATGTGTGCACACAT[A/G]TGTATTTAGGACTCT | 8850 |
rs74849812 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20136547 | TGCATCTTTTTTTTT[C/T]CTTCTGAGATTCTCA | 8850 |
rs74850520 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KAT2B | GRCh38.p7 | 3:20068321 | TAATTTCAACACGTC[C/T]TTACCCACTGCGCTG | 8850 |
rs74948677 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20105499 | AATACAGAGTGGCTG[G/T]GTGCAGTAGCTGATG | 8850 |
rs74951513 | snp | A/C | | | intron-variant | KAT2B | GRCh38.p7 | 3:20144582 | GCGTGAGCCACCAAG[A/C]CCAGCCAGGTTTCTT | 8850 |
rs74983402 | snp | A/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20122179 | CAACATGATCTGTAA[A/G]CTGAAGCTAATGGAG | 8850 |
rs75075007 | snp | A/C | 0.0535932 | 0.154675 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20038375 | CGCACTGTGCCCATT[A/C]CCTAGACTCTATTAT | 8850 |
rs75078775 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20047626 | TTTTTTTTTTTTTTT[G/T]AGACGGAGCCTCACT | 8850 |
rs75085873 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KAT2B | GRCh38.p7 | 3:20065992 | CCACAAAATATGTGG[C/T]TTAAAACAACAAATA | 8850 |
rs75114118 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20141787 | GAAGTGAGCAAAGGC[C/T]TTTTTTTTTTTTTGG | 8850 |
rs75119235 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | KAT2B | GRCh38.p7 | 3:20083018 | GCTTATTAATTTTCA[A/G]AAGATTGGTTAAATT | 8850 |
rs75154183 | snp | A/G | 0.172351 | 0.237636 | intron-variant | KAT2B | GRCh38.p7 | 3:20043355 | CACAAGTGCATGTGT[A/G]TGTATGCATGTGTTG | 8850 |
rs75200486 | snp | A/G | 0.00809352 | 0.0630972 | intron-variant | KAT2B | GRCh38.p7 | 3:20125861 | ATCCCCACTGTCTTG[A/G]GAGAATAGCTCTGTG | 8850 |
rs75206196 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | KAT2B | GRCh38.p7 | 3:20055851 | GCACTGATCTGATTT[A/G]TGTCACTTTAAGTTA | 8850 |
rs75214106 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | KAT2B | GRCh38.p7 | 3:20098967 | TGTTTCTACTGAAAA[G/T]GCAGTAAGCGAGAAA | 8850 |
rs75232714 | snp | C/T | 0.167484 | 0.23599 | intron-variant | KAT2B | GRCh38.p7 | 3:20069356 | TAGCAAGGTTTGTTA[C/T]GTAGATTCCCCTGGT | 8850 |
rs75268190 | in-del | -/T | 0.173965 | 0.238157 | intron-variant | KAT2B | GRCh38.p7 | 3:20068268 | CCCAAAGTGCTGCAA[-/T]TATAGGTGTGAGCCA | 8850 |
rs75300414 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20069544 | CTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 8850 |
rs75316982 | snp | A/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20139060 | CACCATGCCCAGCAA[A/T]TTTTTTTTTTTAATC | 8850 |
rs75350343 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20136368 | GTCTTCTGGCTGATT[C/T]AGAGATTCTGGGCTT | 8850 |
rs75365538 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KAT2B | GRCh38.p7 | 3:20091929 | ACCAGTGTGGTTGGA[A/G]TAGACAGTTGGTATG | 8850 |
rs75439106 | snp | C/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20059446 | AAAAAGGCCAGGCGT[C/G]GTGCCTCACGCTTGT | 8850 |
rs75456100 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KAT2B | GRCh38.p7 | 3:20068701 | TGTAGTAGGCCTCAA[C/T]AAATATTGTTGAAAG | 8850 |
rs75468927 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20136527 | GAAGATTAGCACTTT[C/T]CATTTGCATCTTTTT | 8850 |
rs75473972 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KAT2B | GRCh38.p7 | 3:20064725 | CTTTACTTACATCGA[C/G]TGAGATAAGAGTACA | 8850 |
rs75482782 | snp | G/T | 0.0704125 | 0.17392 | intron-variant | KAT2B | GRCh38.p7 | 3:20121377 | TTCAAAAAATTTACT[G/T]GTAAAAATAAATACA | 8850 |
rs75513656 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KAT2B | GRCh38.p7 | 3:20100164 | TTTAGGGTTGTTACA[C/T]ACTCACAGTTTACTG | 8850 |
rs75518055 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | KAT2B | GRCh38.p7 | 3:20103526 | GCAATTCATCTATCT[C/T]AGCCTCCTTAGTAGC | 8850 |
rs75587570 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | KAT2B | GRCh38.p7 | 3:20104674 | AGAACAAAGATGTGC[C/T]GAAAATGTTTGCAGT | 8850 |
rs75616454 | snp | A/T | 0.136166 | 0.22258 | intron-variant | KAT2B | GRCh38.p7 | 3:20087168 | TGACTGTGGTTAACA[A/T]TAATATCTAGTTTCA | 8850 |
rs75667402 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20046045 | AGCCTCAATGACTGC[A/G]TGTATAAAGTGGTGA | 8850 |
rs75731241 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20141786 | GGAAGTGAGCAAAGG[C/T]TTTTTTTTTTTTTTG | 8850 |
rs75780220 | snp | A/G | 0.0189856 | 0.0955633 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20154038 | CCATGAGTGGTGTCT[A/G]GATTTCTAATGAAGA | 8850 |
rs75782282 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | KAT2B | GRCh38.p7 | 3:20090255 | AAAGAAGTGGCAAGG[G/T]TGGGTATATTTTTCT | 8850 |
rs75824895 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | KAT2B | GRCh38.p7 | 3:20059906 | CCTGTTCCTACCCCC[A/C]ACCCCAGATGACCAC | 8850 |
rs75827295 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20078892 | CTTTTTTTTTTTTTT[G/T]GAGAAGGAGTCTCAC | 8850 |
rs75861167 | snp | G/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20144305 | TTTTTTTTTTTTTTT[G/T]TGAGACAGCGTCTCA | 8850 |
rs75870092 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20140887 | TGTAAAATACAAAAT[A/G]TGTAAAATACAAAAT | 8850 |
rs75914618 | snp | C/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20144289 | TTCTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 8850 |
rs75922242 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | KAT2B | GRCh38.p7 | 3:20043234 | TATGTATCCATTCAT[G/T]CAGTAAATATTTAGA | 8850 |
rs75973048 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KAT2B | GRCh38.p7 | 3:20048694 | TCTGTCGTTAAGAGA[A/G]AAGTGGCTATTTAGG | 8850 |
rs75997980 | snp | A/G | 0.191147 | 0.242974 | intron-variant | KAT2B | GRCh38.p7 | 3:20049583 | GTCGCTTTTCTTCCA[A/G]ATGGTTTCTTGAGAG | 8850 |
rs76009386 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20044069 | CAGAGAATAGAAAAA[A/G]AAAAAAAAAAAAGAA | 8850 |
rs76013046 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | KAT2B | GRCh38.p7 | 3:20117167 | ACATTGTTATCTGTC[A/G]TAGTACAGGATGGAG | 8850 |
rs76022842 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KAT2B | GRCh38.p7 | 3:20142086 | CTAATTCATCCCCAC[A/G]GTGTTAGCTGAGAGC | 8850 |
rs76025131 | snp | A/G | 0.029116 | 0.117091 | intron-variant | KAT2B | GRCh38.p7 | 3:20105394 | AACAGTCTGCTGAAG[A/G]AAAGTGCAAGTAATT | 8850 |
rs76084022 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20050720 | CTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 8850 |
rs76097813 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | KAT2B | GRCh38.p7 | 3:20089970 | CAACATAGTGAGAAG[C/G]CATCTCTATTAAAAA | 8850 |
rs76101657 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | KAT2B | GRCh38.p7 | 3:20048769 | TGTGGTCATCTGATT[A/C]AAACGGGGAATTAGA | 8850 |
rs76116962 | snp | C/T | 0.331642 | 0.236293 | intron-variant | KAT2B | GRCh38.p7 | 3:20079707 | TACCATATAATTGCC[C/T]CCTCAGTTCCCATTT | 8850 |
rs76117137 | snp | C/T | 0.114387 | 0.210022 | intron-variant | KAT2B | GRCh38.p7 | 3:20123359 | TTAGAAAATTTAGCC[C/T]GGTTACAATATTTTC | 8850 |
rs76131221 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20055883 | TTTAGCTATTTTTCA[G/T]ATAAATGTTACCACA | 8850 |
rs76179565 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20078551 | CTAATTTTTTTTTTT[G/T]GTATCTTTGGTAGAG | 8850 |
rs76193978 | snp | A/G | 0.248755 | 0.249997 | intron-variant | KAT2B | GRCh38.p7 | 3:20078350 | ATTTGTCTAGTAATA[A/G]TATTTTAGTTTAGAG | 8850 |
rs76209276 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20098249 | TAAAAAAAAAAAAAA[G/T]TCAGTCTTAGATGTT | 8850 |
rs76244030 | snp | A/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20098250 | AAAAAAAAAAAAAAG[A/T]CAGTCTTAGATGTTG | 8850 |
rs76281300 | in-del | -/TTT/TTTATTT/TTTATTTATTTTTTT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20092235 | TTTATTTATTTATTT[-/TTT/TTTATTT/TTTATTTATTTTTTT]ATTTATTTGAGATGG | 8850 |
rs76326519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20110758 | CACTGTATGTTGGCC[A/G]AATGCACTTTCTAAA | 8850 |
rs76379975 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KAT2B | GRCh38.p7 | 3:20109495 | CTGATTTTTAAACTT[C/T]TTGTAGAGATGGGCR | 8850 |
rs76451200 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KAT2B | GRCh38.p7 | 3:20094447 | AGACACAGAGCCAAA[C/T]CATATCAGAGCCTTA | 8850 |
rs76516479 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | KAT2B | GRCh38.p7 | 3:20117088 | GTGGAGAGGATTTCT[G/T]TGTGTGAAAACTCCC | 8850 |
rs76536306 | snp | A/T | 0.400504 | 0.199621 | intron-variant | KAT2B | GRCh38.p7 | 3:20075925 | AAAAAAAAAAAAAAA[A/T]TTTTTTCATACGGCT | 8850 |
rs76540509 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | KAT2B | GRCh38.p7 | 3:20089218 | CTATTTGGAGTCTTA[C/T]GTAGTTCTGTACAGA | 8850 |
rs76555635 | snp | A/G | 0.000150031 | 0.00865984 | intron-variant | KAT2B | GRCh38.p7 | 3:20095454 | TCTCATTATTCAAAT[A/G]TACCCAGTCTCCATA | 8850 |
rs76706807 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20063548 | TCTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTT]GAGATGGTTGCTCTG | 8850 |
rs76748926 | snp | C/T | 0.137187 | 0.223099 | intron-variant | KAT2B | GRCh38.p7 | 3:20122259 | CACATTTACAAAAGA[C/T]TGGTCTTATTTTAGG | 8850 |
rs76854494 | snp | C/G | 0.189576 | 0.242588 | intron-variant, downstream-variant-500B | KAT2B, MIR3135A | GRCh38.p7 | 3:20138004 | TAAAATAAGTTTTCA[C/G]CTCAGCTTTTTGAGG | 8850 |
rs76868587 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20058372 | AGGCAGGAGAATTGC[C/T]TGAACCTGGGAGGCG | 8850 |
rs76887694 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KAT2B | GRCh38.p7 | 3:20082718 | TTAAAGAACTGCCAA[C/T]GTAGATATGGCTTTC | 8850 |
rs76960730 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | KAT2B | GRCh38.p7 | 3:20051439 | TTGCCACTTGTCCCT[A/G]GTTCTGGAAGATGAC | 8850 |
rs76961364 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KAT2B | GRCh38.p7 | 3:20088288 | GTGGAATTGCTGGGT[C/T]AGGTCATATGGTAGT | 8850 |
rs76975917 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KAT2B | GRCh38.p7 | 3:20121006 | TCATAAACACCATTA[C/G]CAGTCTAACAAGCAG | 8850 |
rs76989272 | snp | A/C | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20051199 | AGCAATACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 8850 |
rs76999560 | snp | C/T | 0.287085 | 0.247234 | intron-variant | KAT2B | GRCh38.p7 | 3:20088454 | TAGCTATCCTGAGCG[C/T]GAAGTGATATCTCAT | 8850 |
rs77029199 | snp | A/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20064012 | TTGGCACACTTGTCA[A/G]AATCATTTGACCATT | 8850 |
rs77047381 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20085525 | TCTTTTTTTTTTTTT[G/T]TGCAGGGGGCAGAGT | 8850 |
rs77057204 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KAT2B | GRCh38.p7 | 3:20097783 | CTCAAGTGATCTCCC[A/C]CCTCGGCCTTCCAAA | 8850 |
rs77109672 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20116092 | TGTCCTTTTTTTTTT[C/T]CTAACCTGAGATCGT | 8850 |
rs77110115 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | KAT2B | GRCh38.p7 | 3:20051831 | TAGTCTTTTCCGTAA[C/T]TGGTATATTTAACAA | 8850 |
rs77150935 | snp | A/T | 0.206642 | 0.246211 | intron-variant | KAT2B | GRCh38.p7 | 3:20129231 | TATGTATATATTTTT[A/T]AAAAAGCAAGTGGAA | 8850 |
rs77170994 | snp | A/T | 0.252702 | 0.249985 | intron-variant | KAT2B | GRCh38.p7 | 3:20078286 | GGAATTTCTATTGTT[A/T]TTTTGGAGTCCATTG | 8850 |
rs77232235 | snp | A/G | 0.135143 | 0.222054 | intron-variant | KAT2B | GRCh38.p7 | 3:20143320 | GAGATGCAAGTCAAA[A/G]CCACAATGTGATACT | 8850 |
rs77242204 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20088533 | CATATACCTGTTGGC[C/T]ATTTGTATGTCTTCT | 8850 |
rs77262827 | in-del | -/GAA | 0.46855 | 0.121392 | intron-variant | KAT2B | GRCh38.p7 | 3:20113944 | GTTCAGGGAAAAAAT[-/GAA]GAAGAAGACCACTGA | 8850 |
rs77271589 | snp | C/T | 0.136506 | 0.222754 | intron-variant | KAT2B | GRCh38.p7 | 3:20135425 | TTTGGGAGGCCGAGA[C/T]GGGCAGATCACAAGG | 8850 |
rs77295528 | snp | A/C/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20106366 | CATGTGCTCATGCAC[A/C/G]TCCGTTTCCTTCTTT | 8850 |
rs77307755 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KAT2B | GRCh38.p7 | 3:20117051 | TTCAGCAGGATCAAC[A/G]TAGTTCTCCTGTGGT | 8850 |
rs77335942 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | KAT2B | GRCh38.p7 | 3:20140020 | CATTTAAAAAATGTT[C/G]TCTTGCTTCCTATTT | 8850 |
rs77384829 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | KAT2B | GRCh38.p7 | 3:20055553 | TGAGGAAGAGGGTGC[C/T]GTGCAAAGACTCTGG | 8850 |
rs77464022 | snp | A/G | 0.287606 | 0.247155 | intron-variant | KAT2B | GRCh38.p7 | 3:20086161 | CCTGTAGTCCCAGCT[A/G]TTTGGGAGACTGAGG | 8850 |
rs77464999 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20136548 | GCATCTTTTTTTTTT[C/T]TTCTGAGATTCTCAA | 8850 |
rs77481541 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | KAT2B | GRCh38.p7 | 3:20128213 | AAAATAGATCTCAGT[A/G]TTCATTGTTAATTTA | 8850 |
rs77510832 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KAT2B | GRCh38.p7 | 3:20055024 | CAATGCAGAGAGAAA[C/T]CATTGTGAGCCAGGG | 8850 |
rs77582949 | snp | G/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20089417 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA | 8850 |
rs77590524 | snp | A/G | 0.3752 | 0.216391 | intron-variant | KAT2B | GRCh38.p7 | 3:20109268 | TAGTTATTTGATCTG[A/G]CTTCCCCTCAGCCCC | 8850 |
rs77606263 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KAT2B | GRCh38.p7 | 3:20151167 | GAAGAAAGAAAAGTT[C/G]AAAGTTGAATTTACA | 8850 |
rs77629342 | snp | C/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20041931 | GGAGCTTCTCAGTCA[C/G]AATGGAATGTCTATG | 8850 |
rs77670027 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KAT2B | GRCh38.p7 | 3:20073739 | ATAAATAAAACAGAA[C/G]GAAACAAAACAATCA | 8850 |
rs77820109 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20142845 | CTATTTGAGAAAGCG[C/T]GAATAGGCTATGAGC | 8850 |
rs77851264 | snp | C/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20075370 | TTTTTTCTTCACTCA[C/G]CAAGCAATTCTCCCA | 8850 |
rs77947005 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | KAT2B | GRCh38.p7 | 3:20081109 | ATTTCATTGTAGTCA[C/T]TAATTTTACCTCTTC | 8850 |
rs77958773 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KAT2B | GRCh38.p7 | 3:20103790 | ACTTATGAATACTTA[A/G]GAAGTAGTAAAAATG | 8850 |
rs78008890 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | KAT2B | GRCh38.p7 | 3:20134250 | GTTTATTTTACCTTA[C/G]ATTTAGATTTCTAAT | 8850 |
rs78047130 | in-del | -/AA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20141378 | AAGGCAGAAAAAAAA[-/AA]CACTCATGATGAAAA | 8850 |
rs78131327 | snp | A/G | 0.234692 | 0.249531 | intron-variant, upstream-variant-2KB | KAT2B, MIR3135A | GRCh38.p7 | 3:20135672 | AAAAAAAAAATAAAA[A/G]CCAAAGTGATTAGTT | 8850 |
rs78147783 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | KAT2B | GRCh38.p7 | 3:20098323 | ATCTTAGTGCTTACA[A/C]ATGTGGCGCTGGAGT | 8850 |
rs78148265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20088101 | AGTTTTTAAGGCTGA[A/G]TAGTATTTGATTGTG | 8850 |
rs78154827 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | KAT2B | GRCh38.p7 | 3:20114665 | GTGCTGTGTTAAGCT[A/T]TGCAGGGTCAAAAGA | 8850 |
rs78168290 | snp | A/C | 0.308661 | 0.24302 | intron-variant | KAT2B | GRCh38.p7 | 3:20120992 | CTTTTTAAAAAAAAT[A/C]ATAAACACCATTAGC | 8850 |
rs78221220 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | KAT2B | GRCh38.p7 | 3:20085018 | CTTGATATTGTATAC[G/T]GATTGCTTTCATAGC | 8850 |
rs78283823 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | KAT2B | GRCh38.p7 | 3:20083104 | CTACTGATACAGTGT[A/T]CATTGATGCACATCT | 8850 |
rs78375065 | snp | C/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20144284 | TGGGATTCTTTTTTT[C/T]TTTTTTTTTTTTTTT | 8850 |
rs78378591 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KAT2B | GRCh38.p7 | 3:20124181 | AACATTACAGATTAG[C/G]TGAGTTTAGGTTTTT | 8850 |
rs78379434 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KAT2B | GRCh38.p7 | 3:20092695 | TTTTGGTCTCTGTAT[C/T]GTTTTTTGTTGTTGT | 8850 |
rs78413907 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | KAT2B | GRCh38.p7 | 3:20084370 | CCTACCACTCCAGAC[C/G]TGCGTTTATTTCATT | 8850 |
rs78441191 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20039596 | ACCCAGAAATTGCTA[C/T]GGGAAGAAAGTGTTA | 8850 |
rs78443473 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KAT2B | GRCh38.p7 | 3:20049809 | CACTGTGCTGGCCCA[A/G]TAGAATTCTCTGTTG | 8850 |
rs78456400 | snp | A/G | 0.133777 | 0.221342 | intron-variant | KAT2B | GRCh38.p7 | 3:20151161 | TTTAGAGAAGAAAGA[A/G]AAGTTGAAAGTTGAA | 8850 |
rs78469082 | snp | A/G | 0.231111 | 0.249285 | intron-variant | KAT2B | GRCh38.p7 | 3:20106963 | CTGAATTTTATGTGT[A/G]TATATATATATATAT | 8850 |
rs78512095 | snp | C/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20143941 | CAGGTACTGTGCTCA[C/G]TACTTGGGCAGTGAG | 8850 |
rs78525532 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20057264 | GAGGGCAAGCCTTTT[G/T]GTAAAACTGACTGGG | 8850 |
rs78574503 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | KAT2B | GRCh38.p7 | 3:20061262 | CTATTTTACTTAGCA[G/T]AACATTCTCAAGTTT | 8850 |
rs78595344 | snp | A/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20096603 | CTAATAAGAAGCACT[A/G]TGCTTCATTTTATAA | 8850 |
rs78622065 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KAT2B | GRCh38.p7 | 3:20061150 | ACTCCCTCTTCCTTC[A/C]TCCAACCCCTCGGCA | 8850 |
rs78667444 | snp | A/G | 0.345037 | 0.231231 | intron-variant | KAT2B | GRCh38.p7 | 3:20063213 | GCTGTGACTGCAGGC[A/G]TGCACCACTATGTCC | 8850 |
rs78684476 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | KAT2B | GRCh38.p7 | 3:20104369 | ACCAACCTCCCCCAC[A/G]TCCCCACCATCACGT | 8850 |
rs78699704 | snp | A/G | 0.20111 | 0.245173 | intron-variant | KAT2B | GRCh38.p7 | 3:20144444 | CAGGCACCCGCCACC[A/G]TGCCCAGCTAATTTT | 8850 |
rs78778598 | snp | G/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20107823 | TTTTTTTTTTTTTTT[G/T]TTTGAGTTGGAGTCT | 8850 |
rs78785353 | snp | A/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20055113 | GCAGAGAAGCAAAAC[A/T]GTTGTGAGCCAGACG | 8850 |
rs78798359 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | KAT2B | GRCh38.p7 | 3:20098966 | TTGTTTCTACTGAAA[A/C]GGCAGTAAGCGAGAA | 8850 |
rs78844889 | snp | G/T | 0.0948562 | 0.196037 | intron-variant | KAT2B | GRCh38.p7 | 3:20102179 | AAATTAACTGGGCAT[G/T]GTGTCACGTGACTGT | 8850 |
rs78895864 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | KAT2B | GRCh38.p7 | 3:20047492 | TATAGATCATAAAAC[C/T]TGCCCACTGTAACTA | 8850 |
rs78923857 | snp | G/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20150884 | CCCCCTCCCCCTTTT[G/T]GGGGGGTACATGTTT | 8850 |
rs78994263 | snp | C/T | 0.190205 | 0.242744 | intron-variant | KAT2B | GRCh38.p7 | 3:20138451 | GTGTGTGTTTGTGTA[C/T]ATGTTTTGCCCTCAT | 8850 |
rs79025291 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | KAT2B | GRCh38.p7 | 3:20078808 | TTTCTTTTCTGTTAA[C/G]TTTTAAAATTTTGAG | 8850 |
rs79027229 | snp | C/T | 0.18989 | 0.242666 | intron-variant | KAT2B | GRCh38.p7 | 3:20138871 | ATTACATAAAATCTA[C/T]TGACTTGTTTTGGTT | 8850 |
rs79050286 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | KAT2B | GRCh38.p7 | 3:20117782 | AGTGTTATTGAGAAT[C/G]TCTGTACCCCTTGTC | 8850 |
rs79070334 | snp | A/G | 0.135143 | 0.222054 | intron-variant | KAT2B | GRCh38.p7 | 3:20144224 | TTTCAAATTGAAACA[A/G]TCTTCAGCATATTCT | 8850 |
rs79073219 | snp | C/T | 0.144969 | 0.226867 | intron-variant | KAT2B | GRCh38.p7 | 3:20124584 | GCCCCACCTCCAACA[C/T]TGGAGATTGCATTTC | 8850 |
rs79085995 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | KAT2B | GRCh38.p7 | 3:20056323 | AAGGATAATGTCCAG[G/T]TTTTTGGCCTGAGCA | 8850 |
rs79098655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT2B | GRCh38.p7 | 3:20093814 | TGCCGCCTCCTGTTA[C/T]GTGGCAAACGTAGTA | 8850 |
rs79153033 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KAT2B | GRCh38.p7 | 3:20101187 | AATAGAGAAATGTCT[A/G]TTATTTTGCTAATAA | 8850 |
rs79185862 | snp | C/G/T | 0.0448719 | 0.142907 | intron-variant | KAT2B | GRCh38.p7 | 3:20087666 | TCTACCCGTACCTCA[C/G/T]GTTCCAAGTCCCTAA | 8850 |
rs79198605 | snp | A/C | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20058420 | AGATTGCGCCACTGC[A/C]CCGTAGCCTGGGCAA | 8850 |
rs79230681 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20069820 | AGGTGTGAGCCACTG[A/C]GCCCGGCCAAGCTTT | 8850 |
rs79240974 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | KAT2B | GRCh38.p7 | 3:20115369 | GAAGGAAGACAGATG[C/T]CTTCTGGAGTCGCAG | 8850 |
rs79247024 | snp | A/G | 0.0644693 | 0.167566 | upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20039042 | CACACCCCTTAAAGC[A/G]TCTGGCCTGAGAGCT | 8850 |
rs79262878 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | KAT2B | GRCh38.p7 | 3:20101217 | ACCACCAATCATGCT[G/T]GCTGTGTGGGTGTTC | 8850 |
rs79263632 | in-del | -/CAT | | | intron-variant | KAT2B | GRCh38.p7 | 3:20104007 | GAAGATGCTCATCAT[-/CAT]TTTCCTCCCATGCAC | 8850 |
rs79320914 | snp | A/C | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20110672 | AGTGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 8850 |
rs79337773 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | KAT2B | GRCh38.p7 | 3:20046461 | ATGGTGCGTGCCTGT[A/G]GTCCCTAGCTACTCA | 8850 |
rs79359650 | snp | A/G | 0.5 | 0 | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154902 | AAAAAAAAAAAAAAA[A/G]GGCATATGATGGCCA | 8850 |
rs79379431 | snp | A/C | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20051200 | GCAATACTCTGTCTC[A/C]AAAAAAAAAAAAAAC | 8850 |
rs79410556 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | KAT2B | GRCh38.p7 | 3:20049685 | GGATTTTCTAGTCCA[C/T]TGAACCTGTGCAGGC | 8850 |
rs79411532 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KAT2B | GRCh38.p7 | 3:20079971 | CCCTGACGTCCTCTG[A/G]TCATGAAATCCTGTT | 8850 |
rs79525585 | snp | A/C | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20118731 | AACTTTGTCTCAAAA[A/C]AAAAAAAAAAAAAAA | 8850 |
rs79537479 | snp | G/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20144301 | TTTTTTTTTTTTTTT[G/T]TTTTTGAGACAGCGT | 8850 |
rs79727649 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | KAT2B | GRCh38.p7 | 3:20060014 | ATGGGCTTCTTATGC[C/T]GAGTGTAATGTGTTT | 8850 |
rs79733891 | snp | A/G | 0.078151 | 0.181571 | intron-variant | KAT2B | GRCh38.p7 | 3:20102417 | TAAATAACATTTTAC[A/G]TTAGTTATAATGAAA | 8850 |
rs79816598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20066971 | TTAAAGACTCCGTAT[G/T]CGCTTGTGGCTGGCT | 8850 |
rs79843886 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KAT2B | GRCh38.p7 | 3:20105395 | ACAGTCTGCTGAAGG[A/G]AAGTGCAAGTAATTA | 8850 |
rs79856220 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | KAT2B | GRCh38.p7 | 3:20133210 | TGAACTTACAGGTAA[G/T]AGGTGACTGTGTGTT | 8850 |
rs79861488 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20050721 | TTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 8850 |
rs79867862 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KAT2B | GRCh38.p7 | 3:20091224 | TATATTTTCATGATT[C/T]AGTTTTGGTAGGTTG | 8850 |
rs79907535 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KAT2B | GRCh38.p7 | 3:20097741 | GGGGTTTCACATTGT[C/T]GGCCACGCTTGTCTT | 8850 |
rs79972869 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KAT2B | GRCh38.p7 | 3:20048126 | ATTGTATCCTGTGGT[A/G]ACTTCTCTAAAATGC | 8850 |
rs79991131 | snp | C/T | 0.303938 | 0.244112 | intron-variant | KAT2B | GRCh38.p7 | 3:20122244 | TCCAAGAAGACACTG[C/T]ACATTTACAAAAGAT | 8850 |
rs79997344 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KAT2B | GRCh38.p7 | 3:20092573 | TATTATATATATATT[C/T]TATATATTTACAGCA | 8850 |
rs80045044 | snp | A/C | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20051201 | CAATACTCTGTCTCA[A/C]AAAAAAAAAAAAACC | 8850 |
rs80045752 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | KAT2B | GRCh38.p7 | 3:20141968 | GAGCTTAATGAGCAG[G/T]TCTGGATTCAGCAGC | 8850 |
rs80073203 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KAT2B | GRCh38.p7 | 3:20152256 | CCAACAACATAGATT[C/T]CTTTCCCAGTCCCAG | 8850 |
rs80100123 | in-del | -/GC/GTGC/TG | | | intron-variant | KAT2B | GRCh38.p7 | 3:20130870 | TGTGTGTGTGTGTGT[-/GC/GTGC/TG]GCGTGCATGTGTGTG | 8850 |
rs80219621 | in-del | -/CAAAA | | | intron-variant | KAT2B | GRCh38.p7 | 3:20059412 | ACAGAGACTCTGTCT[-/CAAAA]AAAAAAAAAAAAAAA | 8850 |
rs80250141 | snp | A/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20043728 | CAGATTTGCTTTTTT[A/T]AAAAAAAAAAAAAAT | 8850 |
rs80259727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20086417 | TAGCCTGGGCAACAT[A/G]GTGAAACTTTGCGCC | 8850 |
rs80265746 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | KAT2B | GRCh38.p7 | 3:20120983 | AGCCTCAGACTTTTT[A/T]AAAAAAATCATAAAC | 8850 |
rs80279438 | snp | G/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20087961 | AAAAAAATTTTTTTT[G/T]GTAGAGACAGGGTCT | 8850 |
rs80311609 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | KAT2B | GRCh38.p7 | 3:20089802 | TTGATGCTGTTATAA[A/G]TGAGATTGTTTCCTT | 8850 |
rs80312435 | in-del | -/AA | | | downstream-variant-500B | KAT2B | GRCh38.p7 | 3:20154901 | TAAAAAAAAAAAAAA[-/AA]GGCATATGATGGCCA | 8850 |
rs80335390 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | KAT2B | GRCh38.p7 | 3:20049708 | GTGCAGGCCATAAAG[C/T]AAACAAAATAAGCAT | 8850 |
rs111215359 | snp | C/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20061995 | AAAACATATAATATA[C/T]AAAACATATAATATA | 8850 |
rs111215361 | snp | A/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20061996 | AAACATATAATATAT[A/G]AAACATATAATATAT | 8850 |
rs111215409 | snp | A/T | | | intron-variant | KAT2B | GRCh38.p7 | 3:20062162 | TAAAAATATATAATA[A/T]ATAATATATATAATA | 8850 |
rs111243566 | snp | A/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20152084 | ATAGGGGATTGAACC[A/G]GATGACTAATAATGG | 8850 |
rs111346762 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KAT2B | GRCh38.p7 | 3:20043540 | AGAACTCTTGGCAGG[A/G]CAGAGTGGGGTGGGG | 8850 |
rs111392228 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20152715 | TGAAGTCATAGGACA[C/T]TTTTATTTTATGGAA | 8850 |
rs111411607 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KAT2B | GRCh38.p7 | 3:20131116 | CGCCTCCTGGGTTCT[A/G]GTGATTCTCCTGCCT | 8850 |
rs111426404 | snp | A/C | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20134829 | CAAAATTTTGAGTAG[A/C]CATATTTAAAAAAGT | 8850 |
rs111443625 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KAT2B | GRCh38.p7 | 3:20059575 | CCAGGTGTGGTGGCG[A/G]GCGCCTGTAGTCCCA | 8850 |
rs111447124 | snp | A/G | 0.461148 | 0.133852 | intron-variant, upstream-variant-2KB | KAT2B | GRCh38.p7 | 3:20070547 | CTGACCTCGTGATCC[A/G]CCCACCTCGGCCTCC | 8850 |
rs111471660 | in-del | -/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20043722 | TTATCTCAGATTTGC[-/T]TTTTTTAAAAAAAAA | 8850 |
rs111502938 | snp | A/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20095057 | TGGGTGGGGAGGCTA[A/G]GGCTCAAGAACATGG | 8850 |
rs111595165 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | KAT2B | GRCh38.p7 | 3:20040447 | CGGCGGCGCCTGACA[A/C]TCGGCGCCTCCTGCC | 8850 |
rs111703472 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KAT2B | GRCh38.p7 | 3:20080545 | TCTAGTTTGTAATAT[A/G]TTTAGTTCGTTGTGC | 8850 |
rs111705396 | snp | A/G | 0.172351 | 0.237636 | intron-variant | KAT2B | GRCh38.p7 | 3:20044252 | TTGGGAGGCCGAGGC[A/G]GGAGGATCACTTGAG | 8850 |
rs111721688 | snp | A/G | 0.236724 | 0.249647 | intron-variant | KAT2B | GRCh38.p7 | 3:20059646 | GGAGGTGGAGCTTGC[A/G]GTGAGCCGAGATCGT | 8850 |
rs111729900 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KAT2B | GRCh38.p7 | 3:20046356 | GGTGGCCAAGGCAGA[C/T]GGATCACTTGAGCTC | 8850 |
rs111756722 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | KAT2B | GRCh38.p7 | 3:20051271 | GTAGATGTAGATAAG[C/G]AATATGAAAGGAAGA | 8850 |
rs111852115 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT2B | GRCh38.p7 | 3:20126776 | GTGGTGAGCCGAGAC[C/T]GTGCCATTGCACTCC | 8850 |
rs111925424 | snp | C/T | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20124988 | GTAGGTCAACAGATA[C/T]TCTCTGGAAAGAAAA | 8850 |
rs111929078 | in-del | -/AGATAGAT | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20109284 | CTTCCCCTCAGCCCC[-/AGATAGAT]AGATAGATAGATAGA | 8850 |
rs111932878 | snp | A/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20143058 | TGCAATTTTTTTATA[A/T]GGAGACATGCAAAGA | 8850 |
rs111953193 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT2B | GRCh38.p7 | 3:20083813 | AGGAATGAATGATGG[A/G]CTTGTTGGCAGAAAC | 8850 |
rs112066401 | snp | C/T | 0.117537 | 0.212022 | intron-variant | KAT2B | GRCh38.p7 | 3:20058479 | AAAAAAAAAAAAGGT[C/T]TTCAGAGATGCTTCT | 8850 |
rs112075281 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KAT2B | GRCh38.p7 | 3:20042066 | GCTCCTCAAACTTTA[A/G]TGTGCATGGGAATCT | 8850 |
rs112082681 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | KAT2B | GRCh38.p7 | 3:20043593 | ACTGAAAGCAGTTGT[-/G]GAAGCTTGGAGGTGG | 8850 |
rs112091751 | snp | A/G | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20147499 | AGAACAGGAAATCAC[A/G]TCCAGATCTGTCAGA | 8850 |
rs112146676 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | KAT2B | GRCh38.p7 | 3:20139236 | CTTTTTTTTTAAAAA[C/T]GTGTTCTTATGTAAT | 8850 |
rs112231716 | snp | A/C | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20074189 | ATTAAACTAAAAGGA[A/C]GGTGACAGTGTTTTC | 8850 |
rs112256849 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KAT2B | GRCh38.p7 | 3:20095479 | TCCATATGCCAGGTC[A/G]TGGCTGTGAAGGCTT | 8850 |
rs112268148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20060428 | CCAACAGGGAGAAAC[C/G]CTGTCTCTACTAAAA | 8850 |
rs112295306 | snp | A/C | 0 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20104252 | TGCTGAGAGAAACAG[A/C]AATGAATATGCCCTA | 8850 |
rs112365420 | snp | C/G | | | intron-variant | KAT2B | GRCh38.p7 | 3:20059223 | TTCGAGACCAGCCTG[C/G]CCAACATGGTGAAAC | 8850 |
rs112433349 | in-del | -/AGA | 0.0134861 | 0.0810011 | intron-variant | KAT2B | GRCh38.p7 | 3:20048816 | CTCACACATGGGGAG[-/AGA]AGGAGGGGAATCCTT | 8850 |
rs112439983 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KAT2B | GRCh38.p7 | 3:20138325 | AAGTTGGTTCATACT[A/G]TGTATATAATAATTT | 8850 |
rs112448267 | in-del | -/C | 0.0353433 | 0.12815 | intron-variant | KAT2B | GRCh38.p7 | 3:20047074 | ATGGTTTTTGTTTTG[-/C]CCCCCCCTTTTTTTT | 8850 |
rs112481921 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | KAT2B | GRCh38.p7 | 3:20094234 | TGAAGGAGAAGGAAG[C/G]CAAGTCTTACATGGC | 8850 |
rs112537004 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KAT2B | GRCh38.p7 | 3:20106872 | ATATATAATATGAGC[A/C]AAAAATGCAAGCCAG | 8850 |
rs112550886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KAT2B | GRCh38.p7 | 3:20073033 | TCATTGTCAGTGATG[G/T]CTCAGTAGGCTCTGC | 8850 |
rs112594714 | snp | C/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20063587 | TTGCTCTGTTGCCCA[C/G]GCTGGAATGTAGTGG | 8850 |
rs112615256 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KAT2B | GRCh38.p7 | 3:20124725 | CTGGAATGCACAAGA[A/G]AATTGTTAAATTTTC | 8850 |
rs112636950 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KAT2B | GRCh38.p7 | 3:20151768 | TTAAATGAAGTTTGT[C/T]ATTCTTATTTCATTG | 8850 |
rs112650470 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KAT2B | GRCh38.p7 | 3:20076769 | AAAGTACAAGTTGGG[G/T]TCTAGGGAATTCTGT | 8850 |
rs112702314 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KAT2B | GRCh38.p7 | 3:20075095 | ATGGTGAAACCCCGT[C/G]TCTACTAAAAATACA | 8850 |
rs112703339 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KAT2B | GRCh38.p7 | 3:20061354 | GAATGTATATACTAC[A/G]TTTTACTTATTTATT | 8850 |
rs112741405 | snp | A/T | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20141432 | AAGGCCATTTATTGA[A/T]AGAAAGAACTTTGTG | 8850 |
rs112746461 | snp | A/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20056767 | AGAAGGAGGAGGCAC[A/G]AGGTATTTTAGAATG | 8850 |
rs112792033 | in-del | -/A | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20092235 | TTTATTTATTTATTT[-/A]TTTATTTATTTGAGA | 8850 |
rs112813643 | in-del | -/TATTTATTTATT | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20045318 | CCACTGCACCTGGCC[-/TATTTATTTATT]TATTTATTTATTTAT | 8850 |
rs112875713 | snp | C/G | 0.5 | 0 | intron-variant | KAT2B | GRCh38.p7 | 3:20116523 | GTCCTGGGGTGTGGC[C/G]TGGACATTGGGACTT | 8850 |
rs112899685 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KAT2B | GRCh38.p7 | 3:20112982 | ATAGATGTCATGGGT[A/G]ATTCTGATGGGCTTT | 8850 |
rs112909173 | snp | C/T | 0.146985 | 0.227789 | intron-variant | KAT2B | GRCh38.p7 | 3:20143340 | AATGTGATACTATCT[C/T]ACACCAGTCAGAATG | 8850 |
rs112927228 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KAT2B | GRCh38.p7 | 3:20132802 | ATTTACCAAAGAACC[A/G]TTGTTGTTCTTGAGT | 8850 |