| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs7107 | snp | C/T | 0.187369 | 0.242028 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67983025 | AATAGATTTTACTCA[C/T]TTTAGCCTGGTGCAG | 2186 |
| rs10832 | snp | A/C | 0.187369 | 0.242028 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982735 | TTATAAGAAAAAATA[A/C]TTAGCTGACAAATGA | 2186 |
| rs167532 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67832123 | tcaaactcctgacct[C/T]gtgatccgcctgcct | 2186 |
| rs178338 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67831963 | gtggcataatctcgg[C/T]tcactgcaacctcca | 2186 |
| rs188772 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67832038 | gggactacaggcgcc[C/T]gccaccacgcccgtc | 2186 |
| rs314172 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67831984 | gcaacctccacctcc[C/T]gggttcaagcgattc | 2186 |
| rs1132844 | snp | C/T | 0 | 0 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67983086 | GATTCTAATTTTTTT[C/T]TTTTGTATTAAAATT | 2186 |
| rs1140781 | snp | A/C | 0 | 0 | missense, intron-variant, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67891871 | AATCGGAGAAGTCCA[A/C]CGGGGAGCTAAGTGA | 2186 |
| rs1599859 | snp | C/G | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67841077 | tcgtctaacaactct[C/G]cctaatccagagctt | 2186 |
| rs1966410 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67841099 | CCAGAGCTTGCCAGA[C/T]TTTTTTGGTAAAAGG | 2186 |
| rs1976052 | snp | C/T | 0.417034 | 0.18601 | intron-variant | BPTF | GRCh38.p7 | 17:67834462 | gttactaagatctgt[C/T]tgactttctgcttgt | 2186 |
| rs1976053 | snp | C/G | 0.494484 | 0.0522255 | intron-variant | BPTF | GRCh38.p7 | 17:67836886 | TTTACTGTAATTTCA[C/G]ATACATATTTGAACT | 2186 |
| rs1976054 | snp | G/T | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67837108 | AGGTTAGGACCCTCT[G/T]TAAGGTAAAGACATG | 2186 |
| rs2046323 | snp | G/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67853811 | ATCATTGCTTCTTCG[G/T]ATTATTTTAACTTGA | 2186 |
| rs2052187 | snp | C/T | 0.49263 | 0.0602539 | intron-variant | BPTF | GRCh38.p7 | 17:67838621 | AGCTGGGACTACAGG[C/T]GCTCGCTGCCATGCC | 2186 |
| rs2080090 | snp | A/T | 0.398894 | 0.200825 | intron-variant | BPTF | GRCh38.p7 | 17:67832255 | TGGTTTTTTTTTTTT[A/T]AATTAAGAAACATGC | 2186 |
| rs2086744 | snp | C/G | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67853159 | TACGTTTGTTAAAAA[C/G]AAAACTCTCAGTTAT | 2186 |
| rs2110112 | snp | C/G | 0.353154 | 0.227726 | upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67824064 | TCAAACTCCTGCCCT[C/G]GTGATCCGCCCTCCT | 2186 |
| rs2128792 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67861061 | GGCAGGCACCTCAAA[C/T]GTGTTTAAAACCAAA | 2186 |
| rs2365416 | snp | C/T | | | upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67824747 | AGGTGATCGAAGTCC[C/T]AGCTGGGGCACTGGG | 2186 |
| rs2365417 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67824839 | GTGCGGATTCCACGC[A/C/T]ACAGGTCTTAGGGCG | 2186 |
| rs2365466 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67845013 | ctcccaaagtgctgg[A/G]attacaggcatgagc | 2186 |
| rs2365467 | snp | A/T | 0.494609 | 0.0516363 | intron-variant | BPTF | GRCh38.p7 | 17:67845169 | TTCCATTATTGATAT[A/T]GATCACTTGGTAAAG | 2186 |
| rs2365468 | snp | C/T | 0.494651 | 0.0514399 | intron-variant | BPTF | GRCh38.p7 | 17:67845202 | gacatgtgctagaat[C/T]atccctgtaaaggta | 2186 |
| rs2365764 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67861598 | TGGGATTACAGATGT[A/G]AGCCACCATGCCCAG | 2186 |
| rs3029927 | in-del | -/AGT | 0.494609 | 0.0516363 | intron-variant | BPTF | GRCh38.p7 | 17:67845167 | GTTCCATTATTGATA[-/AGT]TAGATCACTTGGTAA | 2186 |
| rs3205579 | snp | C/T | 0 | 0 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982926 | ATGGTAGATTAAAAT[C/T]AAGCTTGCATAAAGG | 2186 |
| rs3205580 | snp | G/T | 0.0391999 | 0.1344 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982974 | GGACTACAGACTCTG[G/T]TGCCTTGAATATAAC | 2186 |
| rs3205583 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67983020 | TTACTCTGCACCAGG[C/T]TAAAATGAGTAAAAT | 2186 |
| rs3205586 | snp | C/T | | | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67983084 | CAGATTCTAATTTTT[C/T]TCTTTTGTATTAAAA | 2186 |
| rs3206817 | snp | A/G | 0.432944 | 0.170387 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896718 | AATAAATACTCAACT[A/G]TAAATCATAAAACTA | 2186 |
| rs3206818 | snp | C/G | 0.192401 | 0.243274 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896789 | CATTGAAATTTGTCA[C/G]ATGCAATTAAAGACT | 2186 |
| rs3206819 | snp | A/G | 0.224412 | 0.248687 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896874 | ATTAATTAGCTAGGG[A/G]TACATCTCAAGGAAC | 2186 |
| rs3209510 | snp | A/G | 0 | 0 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67983022 | ACTCTGCACCAGGCT[A/G]AAATGAGTAAAATCT | 2186 |
| rs3833111 | in-del | -/AG | | | intron-variant | BPTF | GRCh38.p7 | 17:67826460 | CTCCCCCCCAAACAG[-/AG]GGGAAATGCGACGGC | 2186 |
| rs3935969 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67885843 | AGGCAGACAATTTTT[C/T]GGATACCCCAGAGCT | 2186 |
| rs4020080 | snp | A/G | | | upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67824647 | TTAAGGTTATTTCCC[A/G]ATAATACAAACATTT | 2186 |
| rs4092834 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67856715 | CCTGCTTGAAGCATG[A/G]AGGTCTTGCTGGTGG | 2186 |
| rs4092835 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67856797 | ATTTACTACTTGTAT[C/T]GTCACTTAAATCCTC | 2186 |
| rs4092836 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67856819 | TAAATCCTCAGTTTT[C/T]TGTACAGTACCTTTG | 2186 |
| rs4092837 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67856834 | TTGTACAGTACCTTT[C/G]TTCACAACTGAGCGT | 2186 |
| rs4271626 | snp | C/T | 0.43555 | 0.167544 | intron-variant | BPTF | GRCh38.p7 | 17:67934017 | CACTCTTGTTGCCCA[C/T]GTTGGAGTGCAATGG | 2186 |
| rs4318247 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67886056 | TGTCAGAAAAGACAA[C/T]TGTTTTAGGATTTCA | 2186 |
| rs4337327 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | BPTF | GRCh38.p7 | 17:67907382 | GGTGACAGAGCAAAA[C/G]TCCATCTCAAAAAAA | 2186 |
| rs4371190 | snp | A/G | 0.375 | 0.216506 | intron-variant | BPTF | GRCh38.p7 | 17:67884142 | aaaaaaaaaaaaaaa[A/G]aaagaaagaaaatgc | 2186 |
| rs4468667 | snp | C/T | 0.464947 | 0.127663 | intron-variant | BPTF | GRCh38.p7 | 17:67907513 | caaaaattagctcgg[C/T]gtggtggcgggtact | 2186 |
| rs4517830 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | BPTF | GRCh38.p7 | 17:67844744 | AAAAAAATAAATAAA[A/T]AAATCAGATAAATCC | 2186 |
| rs4569324 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67876634 | ATTTTCAGTAGACAC[A/G]GGGTTTCAACATGTT | 2186 |
| rs4790905 | snp | G/T | 0.481627 | 0.0940692 | intron-variant | BPTF | GRCh38.p7 | 17:67867234 | GAAACAAACTAACAT[G/T]TTGGGGAATATCAGT | 2186 |
| rs4790908 | snp | A/C | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67856791 | ttaagtgacaataca[A/C]gtagtaaatgctgtg | 2186 |
| rs4790941 | snp | C/T | 0.43978 | 0.162738 | intron-variant | BPTF | GRCh38.p7 | 17:67981016 | ACATGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 2186 |
| rs4790973 | snp | A/G | 0.431473 | 0.171952 | intron-variant | BPTF | GRCh38.p7 | 17:67955017 | CAGGCATGAGCCACC[A/G]TACCCGGCCAAAGCT | 2186 |
| rs4790974 | snp | A/T | 0.49607 | 0.0441545 | intron-variant | BPTF | GRCh38.p7 | 17:67954991 | AAGCTTTTAAACATA[A/T]CACAAATATTTTACT | 2186 |
| rs4790981 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | BPTF | GRCh38.p7 | 17:67925718 | AATTTGGTTTATATA[C/T]GATTTTTAAATAGTT | 2186 |
| rs4791044 | snp | A/G | 0.229429 | 0.249152 | intron-variant | BPTF | GRCh38.p7 | 17:67866263 | GACACAAAGAAAAAT[A/G]ACCTCAAAATTCAGA | 2186 |
| rs4791045 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67865086 | gggcacagtggctca[C/T]acctgtaatcccagc | 2186 |
| rs4791046 | snp | C/T | 0.471483 | 0.115954 | intron-variant | BPTF | GRCh38.p7 | 17:67855857 | CCTCTCGACAGCACA[C/T]TGATAAAGTTTCAAC | 2186 |
| rs4791048 | snp | C/T | 0.494568 | 0.0518327 | intron-variant | BPTF | GRCh38.p7 | 17:67852878 | AAAGTGCCAGGATTA[C/T]AGGCGTGAGCCACCG | 2186 |
| rs4791212 | snp | A/G | 0.401392 | 0.198948 | intron-variant | BPTF | GRCh38.p7 | 17:67979269 | TAAACCACCGTGCCC[A/G]GCCCAATGTCATTAT | 2186 |
| rs4791299 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | BPTF | GRCh38.p7 | 17:67934821 | gcgatggcaccatct[C/T]ggctcaccatgacct | 2186 |
| rs4791300 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | BPTF | GRCh38.p7 | 17:67934656 | TTGATCTCTTGACCT[C/T]GTGATCCACCCGCCG | 2186 |
| rs4791301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67925868 | tgacagacagcatca[C/T]acatagaatccaaaa | 2186 |
| rs4791311 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BPTF | GRCh38.p7 | 17:67908356 | accagcccaacaagg[C/T]gaaaccccatctcta | 2186 |
| rs5023499 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | BPTF | GRCh38.p7 | 17:67829844 | TTATTTCTTGTATTA[C/G]GAGTGAGCTATTTCT | 2186 |
| rs5024717 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896468 | GTGCACTGGGGGGAC[A/C/G]GTTTCTAGTTACTCA | 2186 |
| rs5024718 | snp | A/G | 0.497829 | 0.0328757 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896471 | TATGTGCACTGGGGG[A/G]ACAGTTTCTAGTTAC | 2186 |
| rs5821446 | in-del | -/A | 0.496649 | 0.0407971 | intron-variant | BPTF | GRCh38.p7 | 17:67966422 | TTTCTGCTCTAGTAA[-/A]TAGTTACCTAAGATG | 2186 |
| rs6416954 | snp | C/G | 0.134802 | 0.221877 | intron-variant | BPTF | GRCh38.p7 | 17:67974370 | ggcggcctctggtca[C/G]caagaagtgggtggg | 2186 |
| rs6416955 | snp | A/G | 0.18989 | 0.242666 | intron-variant | BPTF | GRCh38.p7 | 17:67974678 | ctacttaggcttacc[A/G]gtttctcaaggacac | 2186 |
| rs6416956 | snp | A/T | 0.154993 | 0.231244 | intron-variant | BPTF | GRCh38.p7 | 17:67975266 | agtggacacttatca[A/T]tccagtcatgaatgg | 2186 |
| rs6416957 | snp | C/G | 0.154993 | 0.231244 | intron-variant | BPTF | GRCh38.p7 | 17:67975268 | tggacacttatcaat[C/G]cagtcatgaatggta | 2186 |
| rs6416958 | snp | C/T | 0.149665 | 0.228982 | intron-variant | BPTF | GRCh38.p7 | 17:67975495 | GTGTGTTTCCTTGAT[C/T]TCAAACCATTTGAAT | 2186 |
| rs6504541 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67838818 | ATTGGAAGAAGTATA[A/G]TTCATTTGCTAAATA | 2186 |
| rs6504542 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67840526 | tccccccttccccct[C/T]ttcctcctctccttc | 2186 |
| rs6504543 | snp | C/T | 0.494484 | 0.0522255 | intron-variant | BPTF | GRCh38.p7 | 17:67841543 | CCTTTTGCTTTTAAT[C/T]TATATATCATGATAT | 2186 |
| rs6504545 | snp | A/G | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67884251 | gctgggattacaggc[A/G]tgcaccaccacacct | 2186 |
| rs6504546 | snp | A/C | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67884269 | caccaccacacctgg[A/C]taatttttgcatttt | 2186 |
| rs6504547 | snp | A/G | 0.126909 | 0.217598 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67886965 | ttaacgtatatcttt[A/G]tgtacttgtgcaggt | 2186 |
| rs6504548 | snp | C/T | 0.494568 | 0.0518327 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67889932 | TGGCAAGATGCTCAG[C/T]ACCCTCTCTCCATTT | 2186 |
| rs6504549 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | BPTF | GRCh38.p7 | 17:67892668 | AATTGCTTAAAAGCA[A/G]TGGCTTTCATACTTC | 2186 |
| rs6504550 | snp | A/G | 0.499897 | 0.00718776 | intron-variant | BPTF | GRCh38.p7 | 17:67898426 | CCAAGAAGGTATTTT[A/G]TCTAAGTTCATTATA | 2186 |
| rs6504551 | snp | G/T | 0.499776 | 0.0105807 | intron-variant | BPTF | GRCh38.p7 | 17:67907210 | aaaaaaaCCTTTAAG[G/T]CCCAAGAATATTCAT | 2186 |
| rs6504552 | snp | A/T | 0.208169 | 0.246476 | intron-variant | BPTF | GRCh38.p7 | 17:67910809 | catctcaaaaaaaaa[A/T]atatatatatataaa | 2186 |
| rs6504553 | snp | C/T | 0.191461 | 0.24305 | intron-variant | BPTF | GRCh38.p7 | 17:67942992 | TCCCATTGTATTCTT[C/T]GTGAATATTGCTCCT | 2186 |
| rs6504554 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | BPTF | GRCh38.p7 | 17:67944489 | GCCTCAAGCCAGTGA[C/G]CTCAACAGTTGACAT | 2186 |
| rs6504555 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | BPTF | GRCh38.p7 | 17:67944611 | GAGAGAAAGGGGGCA[A/G]AAATAATGGTTATCT | 2186 |
| rs6504556 | snp | C/T | 0.190519 | 0.242821 | intron-variant | BPTF | GRCh38.p7 | 17:67945114 | CATTACTGCTTACTG[C/T]AGCCTTGAACTCCTG | 2186 |
| rs6504557 | snp | A/C | 0.137867 | 0.223442 | intron-variant | BPTF | GRCh38.p7 | 17:67947162 | TAGAAGCACTTTTTA[A/C]ACAGCGAAGTTATTT | 2186 |
| rs6504558 | snp | A/G | 0.136506 | 0.222754 | intron-variant | BPTF | GRCh38.p7 | 17:67949294 | cacttgaacccggaa[A/G]gcagaggttgcagtg | 2186 |
| rs6504559 | snp | C/T | 0.135825 | 0.222405 | intron-variant | BPTF | GRCh38.p7 | 17:67955170 | GTGGTGGGCGCTACT[C/T]GGGAGGCTGAGGCAA | 2186 |
| rs6504560 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | BPTF | GRCh38.p7 | 17:67963184 | CTGGAGTTTGCCAGG[A/G]GTAGAATGGTTGGAT | 2186 |
| rs6504561 | snp | C/T | 0.137527 | 0.223271 | intron-variant | BPTF | GRCh38.p7 | 17:67966182 | gtgcttgaatgttat[C/T]taacatcacgtctct | 2186 |
| rs6504562 | snp | C/T | 0.149665 | 0.228982 | intron-variant | BPTF | GRCh38.p7 | 17:67974756 | tgctgtggggagggg[C/T]gtggagtctcccatg | 2186 |
| rs6504563 | snp | C/T | 0.149665 | 0.228982 | intron-variant | BPTF | GRCh38.p7 | 17:67975623 | TACTCTTTTGTTCTT[C/T]ATGAATTGCAAAATA | 2186 |
| rs7206980 | snp | A/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67938184 | ATATATACCTATTGG[A/T]GATCATCTGGGTGGC | 2186 |
| rs7207155 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | BPTF | GRCh38.p7 | 17:67858880 | CTGCCCTTTTTGGCC[A/G]GATACAGACCAAAGG | 2186 |
| rs7207176 | snp | A/G | 0.186105 | 0.241697 | intron-variant | BPTF | GRCh38.p7 | 17:67858910 | GTGTCTTGTCCACAT[A/G]CAGAAAAACCTTGAC | 2186 |
| rs7208663 | snp | C/T | 0.48178 | 0.0936921 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67889055 | GGCCAATAGTCCTAG[C/T]CCTCAGGTGAAGAGT | 2186 |
| rs7208813 | snp | G/T | 0.192088 | 0.2432 | intron-variant | BPTF | GRCh38.p7 | 17:67859029 | AGCCAAGAGcaacat[G/T]tattgagcacttcat | 2186 |
| rs7208909 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67837430 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 2186 |
| rs7208914 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BPTF | GRCh38.p7 | 17:67922525 | GTGGAGGCTTGGAAT[A/G]GTGCTCCAGGTGGAA | 2186 |
| rs7209023 | snp | A/G | 0.190833 | 0.242898 | intron-variant | BPTF | GRCh38.p7 | 17:67922394 | CCCCCTTCTCTGTGC[A/G]GTGATAGGGAAACAC | 2186 |
| rs7209068 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67892499 | CATGGCATCCCAGCT[C/T]TGATCATGAACAATG | 2186 |
| rs7209574 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BPTF | GRCh38.p7 | 17:67862669 | TGCTATAACAAAGTA[C/T]TATACCAAAAAAAAG | 2186 |
| rs7209675 | snp | A/T | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67835142 | ttgagcccaggagtt[A/T]gaggccctagtcagc | 2186 |
| rs7210027 | snp | C/T | 0.492533 | 0.0606443 | intron-variant | BPTF | GRCh38.p7 | 17:67980937 | CCAAAGCAGGCAGTT[C/T]GCTTGAGCCCAGGAG | 2186 |
| rs7212040 | snp | A/G | 0.0569829 | 0.158885 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67889588 | tgagacgggtggatc[A/G]ctggaggtcaggggt | 2186 |
| rs7212293 | snp | A/G | 0.494272 | 0.053207 | intron-variant | BPTF | GRCh38.p7 | 17:67851209 | atgaggtccagtcac[A/G]aggggccttcgtgac | 2186 |
| rs7213292 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67884327 | gccaggctgctctcg[A/G]atgcctgacctcagg | 2186 |
| rs7213405 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67868631 | AAGATTCTGAAAGTA[C/G]ACTTTTAAGTGCCTG | 2186 |
| rs7214758 | snp | C/T | 0.441158 | 0.161117 | intron-variant | BPTF | GRCh38.p7 | 17:67884422 | cccctggcccctccc[C/T]tttttttttttctga | 2186 |
| rs7214985 | snp | A/G | 0.01975 | 0.0973906 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67893585 | ACATAAGTTCTGTCT[A/G]ACTCCAGCAGGAGAG | 2186 |
| rs7216064 | snp | A/G | 0.434976 | 0.168179 | intron-variant | BPTF | GRCh38.p7 | 17:67902693 | CCGTCGTAAAAGTTG[A/G]GAGGGAGAGAAGAAG | 2186 |
| rs7216221 | snp | C/T | 0.196771 | 0.244268 | intron-variant | BPTF | GRCh38.p7 | 17:67856448 | ctttttcctattctt[C/T]gttttggtttttcta | 2186 |
| rs7216621 | snp | A/G | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67865639 | GCTCACTCTCATCGA[A/G]TGCCTCACACATACT | 2186 |
| rs7217111 | snp | A/G | 0.204189 | 0.245767 | intron-variant | BPTF | GRCh38.p7 | 17:67969488 | aaaGAGATAGCCATT[A/G]CTTTTGGTGTGTTCT | 2186 |
| rs7217558 | snp | A/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67881386 | GCTCATGGTATATGG[A/T]TTTTGTACCTTCAGA | 2186 |
| rs7217724 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67881492 | TTTCCATAATCAAGG[G/T]ttttttttttttttt | 2186 |
| rs7217725 | snp | G/T | 0.408163 | 0.193609 | intron-variant | BPTF | GRCh38.p7 | 17:67881495 | CCATAATCAAGGttt[G/T]ttttttttttttttt | 2186 |
| rs7218014 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | BPTF | GRCh38.p7 | 17:67835900 | TTGATTTCCTGACCT[C/T]GTGATCCGCCCACCT | 2186 |
| rs7220916 | snp | A/G | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67961235 | GAGGCACACAGATAC[A/G]TGTGCCCATTCCATC | 2186 |
| rs7221651 | snp | A/G | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67836274 | TTCTGTAATTCACAC[A/G]CTTGGGAAACGGCAT | 2186 |
| rs7222835 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BPTF | GRCh38.p7 | 17:67970574 | ACATTTATTTTCTAA[A/G]AGTACCTAAATGTGT | 2186 |
| rs7222839 | snp | A/C | 0.149999 | 0.229128 | intron-variant | BPTF | GRCh38.p7 | 17:67979295 | gtttacatctgtaat[A/C]ccaacactttggaag | 2186 |
| rs7223357 | snp | C/G | 0.431473 | 0.171952 | intron-variant | BPTF | GRCh38.p7 | 17:67949420 | tctctactaaaaata[C/G]aaaaattagctgggc | 2186 |
| rs7223643 | snp | A/G | 0.481627 | 0.0940692 | intron-variant | BPTF | GRCh38.p7 | 17:67834166 | GTGTTTCCCACCCGT[A/G]TAACCTCCAGGACCA | 2186 |
| rs7223730 | snp | A/G | 0.134802 | 0.221877 | intron-variant | BPTF | GRCh38.p7 | 17:67979576 | ATGACATTGGTTTTC[A/G]ACTTTTAGAATCACC | 2186 |
| rs7223813 | snp | A/G | 0.431621 | 0.171796 | intron-variant | BPTF | GRCh38.p7 | 17:67949724 | atatatataATTTAC[A/G]CATAATTACACAGCT | 2186 |
| rs7223930 | snp | A/G | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67846070 | TTTCTTGAATATAGG[A/G]TAACATTCACTAGTG | 2186 |
| rs7224420 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | BPTF | GRCh38.p7 | 17:67840626 | gcatgatcttggctc[A/G]ctggagcccgtcatt | 2186 |
| rs7224923 | snp | G/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67846149 | CAAATATAAAAGAAG[G/T]TATCCCATTAAAATA | 2186 |
| rs7225316 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BPTF | GRCh38.p7 | 17:67974733 | ggtggagaagatgca[C/T]ggggcaatgctgtgg | 2186 |
| rs7405506 | snp | A/G | 0.134802 | 0.221877 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67984145 | TCTACATTTTAATGA[A/G]TTATAAAATTATTCT | 2186 |
| rs7406143 | snp | C/T | 0.220246 | 0.248223 | intron-variant | BPTF | GRCh38.p7 | 17:67972868 | AGTGTGATGTGTGCG[C/T]TCTTTCCTGAACACC | 2186 |
| rs7406460 | snp | C/G | 0.191461 | 0.24305 | intron-variant | BPTF | GRCh38.p7 | 17:67943453 | TCTGGACAGAAGAGA[C/G]AGCGCCTAGAGAATT | 2186 |
| rs7406952 | snp | C/G | 0.190833 | 0.242898 | intron-variant | BPTF | GRCh38.p7 | 17:67944727 | TCCAGTTCATGACCT[C/G]AGATTGAGAGTGGGT | 2186 |
| rs7501555 | snp | C/T | 0.243061 | 0.249904 | intron-variant | BPTF | GRCh38.p7 | 17:67947067 | GAAACTCACTTATCC[C/T]TCCTTAGCTATAGCC | 2186 |
| rs7501908 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67922763 | TTTGCCAACCACTTT[C/T]TCATGATAGAAGATG | 2186 |
| rs7502482 | snp | A/G | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67951258 | ctgagaatcagcccc[A/G]atcctgaggctctct | 2186 |
| rs7502501 | snp | A/G | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67951344 | gattctgagggtttt[A/G]ggaattgtatgctgg | 2186 |
| rs7502707 | snp | G/T | 0.145642 | 0.227177 | intron-variant, utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67981566 | GATTAGTTAATATAA[G/T]TTTTTAATGTTAAAG | 2186 |
| rs8064784 | snp | C/T | 0.186737 | 0.241863 | intron-variant | BPTF | GRCh38.p7 | 17:67976970 | ATCGCTATAAAATTT[C/T]CAAATGCTAAGAATA | 2186 |
| rs8064993 | snp | A/G | 0.152001 | 0.229992 | intron-variant | BPTF | GRCh38.p7 | 17:67962752 | GGTAGAGATTGAATT[A/G]CTCTATGTACTTTCT | 2186 |
| rs8065275 | snp | C/T | 0.293294 | 0.246223 | intron-variant | BPTF | GRCh38.p7 | 17:67927321 | GGTTATATTGTTACT[C/T]ATCACACCACTGTTG | 2186 |
| rs8065420 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BPTF | GRCh38.p7 | 17:67913632 | TAATGTGAAAATCTT[C/T]CTAATGTAGCTTAGT | 2186 |
| rs8065906 | snp | A/G | 0.397271 | 0.202018 | intron-variant | BPTF | GRCh38.p7 | 17:67906529 | TCACGAGGGTGCCAG[A/G]TGACATAGTGAAGAC | 2186 |
| rs8066686 | snp | A/G | 0.220246 | 0.248223 | intron-variant | BPTF | GRCh38.p7 | 17:67950419 | TTATTTAGCATTTCT[A/G]GAAGTTCTGGCAAAT | 2186 |
| rs8067282 | snp | C/T | 0.228547 | 0.249078 | intron-variant | BPTF | GRCh38.p7 | 17:67876764 | TGAGCTGAGATCGTA[C/T]CACTGCACTCCAGCC | 2186 |
| rs8067729 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | BPTF | GRCh38.p7 | 17:67901897 | TAGGGGGGTACTCCC[C/T]AGGTTTACCAAGAAA | 2186 |
| rs8067892 | snp | A/G | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67841867 | attatctcttttttg[A/G]ggggtttcttctgtt | 2186 |
| rs8068133 | snp | G/T | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67841756 | ttttaaatttaatct[G/T]acagcctcttttaat | 2186 |
| rs8068790 | snp | C/T | 0.0729678 | 0.176521 | intron-variant | BPTF | GRCh38.p7 | 17:67959535 | ATTGTCTTTAATTGA[C/T]AACAGGAAGAGCTGA | 2186 |
| rs8068808 | snp | A/G | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67842167 | Gatacatatagatat[A/G]tatctacatatgctt | 2186 |
| rs8070043 | snp | A/G | 0.221439 | 0.248363 | intron-variant | BPTF | GRCh38.p7 | 17:67898563 | tatcctcccaccttg[A/G]cctcccaaagtgctg | 2186 |
| rs8070191 | snp | A/C | 0.152001 | 0.229992 | intron-variant | BPTF | GRCh38.p7 | 17:67914280 | AAAAGTAAGTACTCT[A/C]TATAAAGGAATTCAT | 2186 |
| rs8070202 | snp | A/G | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67884247 | agtagctgggattac[A/G]ggcatgcaccaccac | 2186 |
| rs8071368 | snp | A/G | 0.220246 | 0.248223 | intron-variant | BPTF | GRCh38.p7 | 17:67957152 | gccgggcgtggtggc[A/G]catgcctgtaatccc | 2186 |
| rs8071463 | snp | A/G | 0.494442 | 0.0524218 | intron-variant | BPTF | GRCh38.p7 | 17:67942539 | gtgggcctatcagtc[A/G]gttcagccattttgg | 2186 |
| rs8071645 | snp | C/G | 0.139742 | 0.224922 | intron-variant | BPTF | GRCh38.p7 | 17:67942680 | catggcataaatatt[C/G]gtagcagcattgttc | 2186 |
| rs8072225 | snp | A/G | 0.49706 | 0.0382258 | intron-variant | BPTF | GRCh38.p7 | 17:67916844 | TCCACCTCTGTTAGA[A/G]GAGGAAATTATTTTT | 2186 |
| rs8072537 | snp | A/G | 0.194278 | 0.243711 | intron-variant | BPTF | GRCh38.p7 | 17:67856921 | CAGCTTGAAGGGGAG[A/G]ATGGTGGTTTAGGAA | 2186 |
| rs8072824 | snp | A/T | 0.116805 | 0.211563 | intron-variant | BPTF | GRCh38.p7 | 17:67886341 | TACTTCATCCATTCC[A/T]TTAAAGGGAAGTTTT | 2186 |
| rs8073510 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67843094 | tatatgtagatacat[A/G]tatctatatatatgt | 2186 |
| rs8074078 | snp | G/T | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67842627 | CGAGACAAAGATTTT[G/T]TGATGACAAAGGCTG | 2186 |
| rs8074644 | snp | C/G | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67882101 | cagcctcccaaagtg[C/G]tagaattacaggcgt | 2186 |
| rs8075984 | snp | A/G | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67900038 | AAATTTTAATGAAGC[A/G]GAAGATTCCAGGAAC | 2186 |
| rs8076388 | snp | A/G | 0.221439 | 0.248363 | intron-variant | BPTF | GRCh38.p7 | 17:67900074 | CAACAAAAACCTCCA[A/G]CACCTAGGAATAATt | 2186 |
| rs8076408 | snp | A/T | 0.0670745 | 0.170406 | intron-variant | BPTF | GRCh38.p7 | 17:67848593 | GGCAAACTTTTTTTT[A/T]AAATTAAAAATATGA | 2186 |
| rs8077757 | snp | A/G | 0.192401 | 0.243274 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67888000 | atggccagggCAGGC[A/G]AGGTACTACGATTGA | 2186 |
| rs8077872 | snp | G/T | 0.494526 | 0.0520291 | intron-variant | BPTF | GRCh38.p7 | 17:67864943 | ccgggtagctgagac[G/T]acaggcgcctgccac | 2186 |
| rs8077942 | snp | C/T | 0.186421 | 0.24178 | intron-variant | BPTF | GRCh38.p7 | 17:67973956 | ATGCTGCCACACTTT[C/T]CATTACCACAGCTTT | 2186 |
| rs8078431 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | BPTF | GRCh38.p7 | 17:67843701 | ctatcacctttgggt[A/G]tgagggtggtctttt | 2186 |
| rs8079078 | snp | A/C | 0.494442 | 0.0524218 | upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67825050 | GTCGCTTGGGCCGCC[A/C]CTCTCCGCGACTTTT | 2186 |
| rs8079291 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67891506 | AATATATAAGGCAAC[A/G]CTTTGTTAGTTTGCT | 2186 |
| rs8079555 | snp | C/G | 0.193028 | 0.243422 | intron-variant | BPTF | GRCh38.p7 | 17:67852864 | GAATGGGCCGGGTGC[C/G]GTGGCTCACGCCTGT | 2186 |
| rs8079754 | snp | A/G | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67891780 | TACGAGTTTTGGTGA[A/G]ATAAGGTGGTTATAA | 2186 |
| rs8079994 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67826845 | GTACACAAACACGCA[C/T]AAAAAAATGCGTTTT | 2186 |
| rs8080440 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67870496 | TTCCCGATTAAAACA[C/T]CAGTTCACCACTGTT | 2186 |
| rs8081066 | snp | G/T | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67950105 | TAAACATTTtaagaa[G/T]gtgagaaatagacca | 2186 |
| rs8081067 | snp | A/G | 0.191147 | 0.242974 | intron-variant | BPTF | GRCh38.p7 | 17:67958765 | aggtcaggagtttgc[A/G]accagcctggccaac | 2186 |
| rs8081517 | snp | A/T | 0.48178 | 0.0936921 | intron-variant | BPTF | GRCh38.p7 | 17:67849581 | AAATAACCTATCAGG[A/T]TATAGGGAGGTGTTT | 2186 |
| rs8081856 | snp | A/G | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67849802 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCACCT | 2186 |
| rs8081964 | snp | C/T | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67849740 | GTGAGGGGTTTGAGA[C/T]CAGCCTGGCCAACAT | 2186 |
| rs8082411 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | BPTF | GRCh38.p7 | 17:67849896 | cagtgagctgagatc[A/G]tgccactgcactcca | 2186 |
| rs8082512 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67840943 | tgtgatgtacatata[C/T]tttctccctgtcagt | 2186 |
| rs8082661 | snp | A/G | 0.417196 | 0.185864 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67888585 | ACAGAACGAGACTCC[A/G]TCTCAAAAAAAAAAA | 2186 |
| rs9674589 | snp | C/G | 0.194278 | 0.243711 | intron-variant | BPTF | GRCh38.p7 | 17:67836032 | AAGGATTAGGATTCA[C/G]AGACTTTTGGTTGAG | 2186 |
| rs9675292 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | BPTF | GRCh38.p7 | 17:67917666 | agacagagtttcact[C/T]ttgtcgcccaggcta | 2186 |
| rs9890622 | snp | A/C | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67891441 | TTTAAACAGAATTTC[A/C]GTGGAAATCTTTCAA | 2186 |
| rs9890629 | snp | A/G | 0.481165 | 0.0951993 | intron-variant | BPTF | GRCh38.p7 | 17:67875443 | TGCTTTAAAATGGCC[A/G]TTCAATGGAAGCAGG | 2186 |
| rs9891128 | snp | C/G | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67833826 | acccgccttggcctc[C/G]caaagtgctgggatt | 2186 |
| rs9891271 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67842314 | TCCTTCTTAAATTTC[C/T]TGTTGCAACTCATGA | 2186 |
| rs9892665 | snp | A/T | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67891472 | AAACTTAAACCTTTT[A/T]ATACAGAAATCCATA | 2186 |
| rs9892730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67939191 | GGAATTTTACCATGG[C/T]GTTAGTTTAACAACA | 2186 |
| rs9892803 | snp | G/T | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67883127 | agaccagcctggcca[G/T]tatagtgaaaccctg | 2186 |
| rs9893181 | snp | C/T | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67906134 | gtcaccaggctggag[C/T]gcagtggcgtatctg | 2186 |
| rs9894079 | snp | C/T | 0.155987 | 0.23165 | intron-variant | BPTF | GRCh38.p7 | 17:67979933 | TAAGTCTCAGCTACT[C/T]GGGAGGCTGAGACAG | 2186 |
| rs9894962 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | BPTF | GRCh38.p7 | 17:67939433 | TAGCTACCAAAAAAT[C/T]ATTCTTAGCAACTGT | 2186 |
| rs9896347 | snp | A/C | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67869826 | GTCTCTACTAAAAAT[A/C]CAAAAAAAAAAAAAA | 2186 |
| rs9896792 | snp | C/T | 0.222333 | 0.248464 | intron-variant | BPTF | GRCh38.p7 | 17:67918534 | TGTTATGCCTATGAA[C/T]GAAGAAGTTTTTCTT | 2186 |
| rs9897042 | snp | C/T | 0.222035 | 0.248431 | intron-variant | BPTF | GRCh38.p7 | 17:67934321 | tcaggagttcgagac[C/T]agcctggccaacatg | 2186 |
| rs9897868 | snp | A/G | 0.136166 | 0.22258 | intron-variant | BPTF | GRCh38.p7 | 17:67905087 | GAAGACGCCTCAGCC[A/G]CCTGATTATCATTTT | 2186 |
| rs9897982 | snp | G/T | 0.494651 | 0.0514399 | intron-variant | BPTF | GRCh38.p7 | 17:67883476 | TGAAAACTATGTAAC[G/T]GGAGATATTCAGAGA | 2186 |
| rs9898736 | snp | A/T | 0.153 | 0.230415 | intron-variant | BPTF | GRCh38.p7 | 17:67892536 | GAGCTAGGACTCGGT[A/T]TCTCTGTGCTTCAGC | 2186 |
| rs9898795 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | BPTF | GRCh38.p7 | 17:67915366 | CTTGGTAACTACTGC[A/G]GCAAGGAGCGGGGAA | 2186 |
| rs9898859 | snp | A/G | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67952533 | ctcccaaagtgctgg[A/G]attccaggcgtgagc | 2186 |
| rs9899296 | snp | G/T | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67876287 | ACTCCAAGTAAGTTA[G/T]AGCACACCAAGAGTG | 2186 |
| rs9899520 | snp | A/G | 0.495891 | 0.0451408 | intron-variant | BPTF | GRCh38.p7 | 17:67961452 | ATTCAAGTCCTGAAC[A/G]TCCTTCCAGAACACA | 2186 |
| rs9899914 | snp | C/T | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67883802 | gacggggtttcacca[C/T]gttggccaggctggt | 2186 |
| rs9900309 | snp | A/G | 0.152334 | 0.230133 | intron-variant | BPTF | GRCh38.p7 | 17:67901345 | AAAACAAAAGAAAAC[A/G]TCAATAAGAAAGCAT | 2186 |
| rs9902203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67852895 | aatcctggcactttg[G/T]caggccgaggtgggt | 2186 |
| rs9902521 | snp | C/T | 0.221439 | 0.248363 | intron-variant | BPTF | GRCh38.p7 | 17:67901808 | CACTGTTCTGAAGAG[C/T]AGTTTGACCCTATAT | 2186 |
| rs9904157 | snp | A/C | 0.0161706 | 0.0884523 | intron-variant | BPTF | GRCh38.p7 | 17:67928624 | ACTATCATTAAGTAA[A/C]AGATTACTTTGGTTC | 2186 |
| rs9905126 | snp | C/T | 0.152667 | 0.230274 | intron-variant | BPTF | GRCh38.p7 | 17:67937349 | gtaatcccagctact[C/T]gggaggctgaggcag | 2186 |
| rs9906619 | snp | C/T | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67877839 | ggtctcactgtgttg[C/T]ccaggccagtctcga | 2186 |
| rs9907491 | snp | A/G | 0.496105 | 0.0439572 | intron-variant | BPTF | GRCh38.p7 | 17:67953877 | gagccactgtgcctg[A/G]ctGTATAATTTCATT | 2186 |
| rs9907983 | snp | G/T | 0.156319 | 0.231784 | intron-variant | BPTF | GRCh38.p7 | 17:67828935 | CCCCCTGCAGCTCCT[G/T]TAACAGAGTTTTGCA | 2186 |
| rs9908145 | snp | A/G | 0.15698 | 0.23205 | intron-variant | BPTF | GRCh38.p7 | 17:67844923 | taattttgtattttt[A/G]gtagagacagcgttt | 2186 |
| rs9909489 | snp | C/G/T | 0.0614748 | 0.164192 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67911547 | TGACTCTAAACTAGC[C/G/T]AGTGCAGATGATATT | 2186 |
| rs9910600 | snp | C/T | 0.221737 | 0.248397 | intron-variant | BPTF | GRCh38.p7 | 17:67920462 | GGTTTATTGAAGTCA[C/T]GGCAGCTAGTACCGA | 2186 |
| rs9911329 | snp | A/G | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67841484 | tattaGCAGTAATAT[A/G]ATACTTTTTTTGACT | 2186 |
| rs9912084 | snp | A/C | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67871919 | CAACCTCTGTCTCCT[A/C]GGTTCAAGCAATTAT | 2186 |
| rs9912770 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67872117 | AGGCGTGAGCCACTG[C/T]GCCCAGCCCTGTTTT | 2186 |
| rs9912971 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67878177 | cctgatagctttttt[C/T]ccacctcaacaaaac | 2186 |
| rs9913471 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67878379 | tttcttgtgcacata[C/T]atgtgcatttctgga | 2186 |
| rs9913627 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | BPTF | GRCh38.p7 | 17:67900127 | ctgtgtgttttgaga[C/T]agagtcttgctgtgt | 2186 |
| rs9914296 | snp | A/C | 0.197082 | 0.244335 | intron-variant | BPTF | GRCh38.p7 | 17:67829540 | TGCCTGGAATGAGTA[A/C]CAATGCATGACAGTG | 2186 |
| rs9914349 | snp | G/T | 0.191147 | 0.242974 | intron-variant | BPTF | GRCh38.p7 | 17:67829265 | TTTCCTTTATTGGCT[G/T]TGATGTTAATTTGGA | 2186 |
| rs9914393 | snp | G/T | 0.19334 | 0.243495 | intron-variant | BPTF | GRCh38.p7 | 17:67938811 | GTAGATGGCAAAGTG[G/T]AAAAAATAGTTTCTA | 2186 |
| rs9914590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BPTF | GRCh38.p7 | 17:67878668 | ctaaggatgttgagc[A/G]tctttatgtgttcgt | 2186 |
| rs9914969 | snp | A/C | 0.136847 | 0.222927 | intron-variant | BPTF | GRCh38.p7 | 17:67894708 | AATTTAAAATATTTT[A/C]TAAAGTAAATAGCAT | 2186 |
| rs9915108 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67878347 | tatgaataatactat[C/T]atgaatattttacat | 2186 |
| rs9915126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67859158 | ttttaattaattaat[C/T]ACttttggagacagg | 2186 |
| rs9915218 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67954324 | aggcatgagccaccg[A/T]actcggccCTGGTTG | 2186 |
| rs9915591 | snp | C/G | 0.482008 | 0.0931261 | intron-variant | BPTF | GRCh38.p7 | 17:67829974 | AAAAATGTAAGGATG[C/G]CAACTTTTTAGTATA | 2186 |
| rs9944426 | snp | C/T | 0.158302 | 0.232576 | intron-variant | BPTF | GRCh38.p7 | 17:67965116 | ggaggctgaggcggg[C/T]ggatcacaaggtcag | 2186 |
| rs10048180 | snp | C/T | 0.0418186 | 0.138422 | downstream-variant-500B | BPTF | GRCh38.p7 | 17:67984519 | CATATGTGTATTTAA[C/T]GGTATAAAGTGTTGT | 2186 |
| rs10445361 | snp | G/T | 0.434109 | 0.169127 | intron-variant | BPTF | GRCh38.p7 | 17:67966122 | CTGTCGTTATCATAA[G/T]CAGAAGAATTGAAGT | 2186 |
| rs10569005 | in-del | -/TA | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67949652 | GTACATATATATATA[-/TA]CACACAGACATATAT | 2186 |
| rs10583750 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67876821 | AAAAAAGTAAAAAAA[A/G]AGAAAAAGAAAATAT | 2186 |
| rs10598085 | in-del | -/AAA | 0.221737 | 0.248397 | intron-variant | BPTF | GRCh38.p7 | 17:67932960 | TATTGGCTTAAAGGT[-/AAA]AAAGATCAGCCAGGC | 2186 |
| rs10618398 | in-del | -/TTC | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67969565 | CCTATGTAAATCTTC[-/TTC]GAAAACCCATGATTT | 2186 |
| rs10626596 | in-del | -/G/GTG/GTGT/GTGTAC | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67944924 | AGGGGACAGCCAAGA[-/G/GTG/GTGT/GTGTAC]AGCAGGGCCCAGGCT | 2186 |
| rs10653000 | in-del | -/GG | | | intron-variant | BPTF | GRCh38.p7 | 17:67913357 | AAAATTGGCCAACTA[-/GG]ATGTACTAAAGTTTT | 2186 |
| rs10657309 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67934889 | AAAAAAAAAAAAAAA[-/A]GCATGTAAGTACATT | 2186 |
| rs10706190 | in-del | -/T | 0.482609 | 0.0916147 | intron-variant | BPTF | GRCh38.p7 | 17:67907257 | TTTTGGGAGGCTTGA[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs10708715 | in-del | -/G | 0.221439 | 0.248363 | intron-variant | BPTF | GRCh38.p7 | 17:67904249 | AGCCAGGTGAGTCTT[-/G]GAACTCCTGACCTCA | 2186 |
| rs10711096 | in-del | -/A | 0.184521 | 0.241273 | intron-variant | BPTF | GRCh38.p7 | 17:67974290 | TGCCTGCTCTACAGC[-/A]AAAAAAAAAACAAAC | 2186 |
| rs10853081 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BPTF | GRCh38.p7 | 17:67936071 | ATGGTTTTACAGGTA[A/T]AGTTCTTGGAAATGG | 2186 |
| rs11079705 | snp | A/T | 0.416545 | 0.186448 | intron-variant | BPTF | GRCh38.p7 | 17:67839336 | CCTAAGTTTTTTTTT[A/T]AAAAAAAATCAGCTA | 2186 |
| rs11079706 | snp | G/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67839354 | AAAAAATCAGCTATG[G/T]CTATTGTATTTTGTC | 2186 |
| rs11079707 | snp | A/G | 0.416708 | 0.186302 | intron-variant | BPTF | GRCh38.p7 | 17:67839501 | CCTTACATTCCTGCA[A/G]CAAACCTCTCTTGAT | 2186 |
| rs11079708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67852181 | AATTTAGTATAATGA[C/T]GTTGTATTTATACAA | 2186 |
| rs11079709 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67857247 | gcttactgcaagctc[C/T]gcctcccgggttcac | 2186 |
| rs11079710 | snp | C/T | 0.450859 | 0.148847 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67889795 | CCTGGGCGACAAGAG[C/T]GAAACTCCATCTCAA | 2186 |
| rs11079712 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | BPTF | GRCh38.p7 | 17:67934643 | cacattgggaggccg[A/G]cgggtggatcacaag | 2186 |
| rs11079713 | snp | A/G | 0.190833 | 0.242898 | intron-variant | BPTF | GRCh38.p7 | 17:67941286 | tgaaattccatctct[A/G]ctaaaagtacaaaca | 2186 |
| rs11283344 | in-del | -/ATTGTC | 0.0803491 | 0.183626 | intron-variant | BPTF | GRCh38.p7 | 17:67917124 | AGTAACTAATATGGT[-/ATTGTC]ATTGTCCTTTTTTTT | 2186 |
| rs11289448 | in-del | -/T | 0.454784 | 0.1434 | intron-variant | BPTF | GRCh38.p7 | 17:67898662 | CGAGTATATGAAGTC[-/T]TTTTTTTTTTTTTTG | 2186 |
| rs11295073 | in-del | -/A | 0.0399052 | 0.1355 | intron-variant | BPTF | GRCh38.p7 | 17:67972245 | TTATTTTATTATTTT[-/A]TTTTTTTTGAGAAGG | 2186 |
| rs11307458 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67944926 | GGGGACAGCCAAGAA[-/G]CAGGGCCCAGGCTTC | 2186 |
| rs11325305 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67862829 | TTTTTTTTTTTTTTT[-/T]GGCCTTTTCTAGCTT | 2186 |
| rs11327848 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67910811 | TCTCAAAAAAAAAAA[A/T]ATATATATATAAATT | 2186 |
| rs11327849 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67910813 | TCAAAAAAAAAAATA[A/T]ATATATATAAATTCC | 2186 |
| rs11354205 | in-del | -/G | 0.191775 | 0.243125 | intron-variant | BPTF | GRCh38.p7 | 17:67955447 | CTTGAAATTTTGGCA[-/G]GGGGGAATCAGGTTT | 2186 |
| rs11360473 | in-del | -/A | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67969475 | AAAAAAAAAAAAAAA[-/A]GAGATAGCCATTGCT | 2186 |
| rs11367624 | in-del | -/T | 0.496681 | 0.0405994 | intron-variant | BPTF | GRCh38.p7 | 17:67848172 | AAACACTGTAAATTC[-/T]TTTTTTTTTTTGAAT | 2186 |
| rs11376410 | in-del | -/A/AA/AAAAAAAAAAAAAAAAAAAAAAGGCCCTGGTTA | 0.483272 | 0.0899109 | intron-variant | BPTF | GRCh38.p7 | 17:67979169 | AAAAAAAAAAAAAAA[lengthTooLong]GGCCCTGTTAGCAAA | 2186 |
| rs11413151 | in-del | -/T/TT | 0.187685 | 0.242109 | intron-variant | BPTF | GRCh38.p7 | 17:67886368 | TTTTTCTTTTTTTTC[-/T/TT]TTTTTTTTGTGTGTG | 2186 |
| rs11414914 | in-del | -/C | 0.479899 | 0.0982164 | intron-variant | BPTF | GRCh38.p7 | 17:67826587 | CTCTCTCCCCCCCCC[-/C]AACCCCCTTTTTTTC | 2186 |
| rs11415470 | in-del | -/T | 0.0879971 | 0.190408 | intron-variant | BPTF | GRCh38.p7 | 17:67909188 | AATCACAGTTTTTTG[-/T]TTTTTTTTTTAATTT | 2186 |
| rs11418428 | in-del | -/T/TT | | | intron-variant | BPTF | GRCh38.p7 | 17:67870787 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTCTCGC | 2186 |
| rs11464478 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | BPTF | GRCh38.p7 | 17:67848584 | AATATGTAGGCAAAC[-/T]TTTTTTTTAAAATTA | 2186 |
| rs11649825 | snp | A/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67904122 | cagcctccgcctcct[A/G]ggttcaaacgattct | 2186 |
| rs11650332 | snp | A/G | 0.465683 | 0.126415 | intron-variant | BPTF | GRCh38.p7 | 17:67979938 | CTCAGCTACTTGGGA[A/G]GCTGAGACAGGAGAA | 2186 |
| rs11652505 | snp | A/C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67923208 | ctacaggtgcatgcc[A/C/T]ccacgcccagctaat | 2186 |
| rs11652543 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | BPTF | GRCh38.p7 | 17:67923212 | aggtgcatgccacca[C/T]gcccagctaatgttt | 2186 |
| rs11652767 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67858579 | aaaaaaaaaaaaaaa[A/G]TTTACTGCTGTGTTG | 2186 |
| rs11653472 | snp | C/T | 0.323197 | 0.239044 | intron-variant | BPTF | GRCh38.p7 | 17:67895892 | CATGAGAAGACATTA[C/T]AGCAGGGTGTTCCTT | 2186 |
| rs11653507 | snp | A/T | 0.497829 | 0.0328757 | intron-variant | BPTF | GRCh38.p7 | 17:67895948 | TTTGGAAACAATTCC[A/T]AAGTACTCAATCAGG | 2186 |
| rs11654278 | snp | A/T | 0.444444 | 0.157135 | intron-variant | BPTF | GRCh38.p7 | 17:67908851 | ttttttttttttttg[A/T]tgacacggagtctca | 2186 |
| rs11654486 | snp | A/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67935401 | cactgcacctccagc[A/C]tgggtgacagagtga | 2186 |
| rs11654786 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67904121 | acagcctccgcctcc[C/T]gggttcaaacgattc | 2186 |
| rs11654980 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67856481 | tcatattcagatgtt[G/T]attaattcttaattt | 2186 |
| rs11656743 | snp | A/G | 0.496746 | 0.040204 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67984173 | TCTGCATCTCATCAC[A/G]TCACAGTATTTCTGT | 2186 |
| rs11657704 | snp | G/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67858580 | aaaaaaaaaaaaaaG[G/T]TTACTGCTGTGTTGT | 2186 |
| rs11657814 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | BPTF | GRCh38.p7 | 17:67844958 | atgttggtcaggctg[A/G]tcacgaacttccaac | 2186 |
| rs11658091 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67832718 | gcatcactccctgtt[C/T]ttcacctccctcctg | 2186 |
| rs11658927 | snp | C/G | 0.139225 | 0.224118 | intron-variant | BPTF | GRCh38.p7 | 17:67896181 | GTTAGCCAGGATGGT[C/G]TCCATCTCCTGACCT | 2186 |
| rs11867401 | snp | A/G | 0.49614 | 0.0437598 | intron-variant | BPTF | GRCh38.p7 | 17:67951854 | TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGCTG | 2186 |
| rs11867517 | snp | C/T | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67879210 | acagtggtgcgatct[C/T]ggctcaccacaacct | 2186 |
| rs11867537 | snp | A/G | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67879376 | tgaactcctgacctc[A/G]tgatccacccgcctc | 2186 |
| rs11867618 | snp | A/G | 0.369346 | 0.219673 | intron-variant | BPTF | GRCh38.p7 | 17:67879471 | CTTAAATGTTTGCTG[A/G]AGTGATTTGGTTCTG | 2186 |
| rs11868959 | snp | C/T | 0.416708 | 0.186302 | intron-variant | BPTF | GRCh38.p7 | 17:67844694 | gggtgaaccactgcg[C/T]ccagtcTgttgcctt | 2186 |
| rs11869819 | snp | A/C | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67872553 | TTTACTAAAAACATA[A/C]AAATTAGCCAGGTGT | 2186 |
| rs11870050 | snp | A/G | 0.0255312 | 0.110063 | intron-variant | BPTF | GRCh38.p7 | 17:67948338 | TTTTCTTCTGTGTCC[A/G]GTGTTTAACATCTGA | 2186 |
| rs11870068 | snp | A/C | 0.432357 | 0.171014 | intron-variant | BPTF | GRCh38.p7 | 17:67948399 | AAAGCTTAAAATTTC[A/C]GTATGTTTTCTAGAA | 2186 |
| rs11871213 | snp | A/C | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67932450 | ctcccctgtaatccc[A/C]ctttggaaggccaag | 2186 |
| rs11871285 | snp | G/T | 0.417034 | 0.18601 | intron-variant | BPTF | GRCh38.p7 | 17:67844693 | ggggtgaaccactgc[G/T]tccagtcTgttgcct | 2186 |
| rs12325877 | snp | A/G | 0.140242 | 0.224618 | intron-variant | BPTF | GRCh38.p7 | 17:67830827 | CTTTTCTGTAGAATA[A/G]GGATTGGGCTGGATT | 2186 |
| rs12325965 | snp | A/G | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67878071 | acacctagcccaaca[A/G]aggtactgactattc | 2186 |
| rs12325985 | snp | A/G | 0.135143 | 0.222054 | intron-variant | BPTF | GRCh38.p7 | 17:67956041 | ACAGGGTCTCGggcc[A/G]ggcgcagtggctcac | 2186 |
| rs12449312 | snp | A/C | 0.48155 | 0.0942576 | intron-variant | BPTF | GRCh38.p7 | 17:67833242 | attgtatggctatac[A/C]gcctttttttttttt | 2186 |
| rs12449442 | snp | A/G | 0.434253 | 0.168969 | intron-variant | BPTF | GRCh38.p7 | 17:67951524 | CCACACACTGTTTCC[A/G]TTCCACATTCTACAC | 2186 |
| rs12450072 | snp | C/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67857401 | tcctgaccttgtgat[C/G]tgtctgcctcggcct | 2186 |
| rs12450117 | snp | A/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67857485 | ttttttttttttgaa[A/G]acaagatctcccttt | 2186 |
| rs12450338 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | BPTF | GRCh38.p7 | 17:67961839 | attagccagatgtgg[C/T]ggcacacacctgtaa | 2186 |
| rs12450363 | snp | C/T | 0.481856 | 0.0935034 | intron-variant | BPTF | GRCh38.p7 | 17:67843992 | ctggtctcaaactcc[C/T]gacctcaggtgatcc | 2186 |
| rs12450907 | snp | G/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67874528 | TATCCGTGACAGATA[G/T]CTATATCAAGGCTAT | 2186 |
| rs12451511 | snp | G/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67878745 | aggtacctgtctgct[G/T]ctttgttcattttct | 2186 |
| rs12451707 | snp | A/G | 0.416218 | 0.186739 | intron-variant | BPTF | GRCh38.p7 | 17:67875482 | GATTATTTAGTAGTT[A/G]ACTGAATGTGGCCAT | 2186 |
| rs12451721 | snp | A/G | 0.397271 | 0.202018 | intron-variant | BPTF | GRCh38.p7 | 17:67942959 | GCTGCTGCATTGCCT[A/G]CCTGGAGGGGGCACT | 2186 |
| rs12451856 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BPTF | GRCh38.p7 | 17:67960800 | ATTGTGGTCCCTTTA[A/G]TGATGTTCAAGTTGC | 2186 |
| rs12451875 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67960764 | ACCTTAAGTGGATAC[C/T]TAATTGATTCCTAAA | 2186 |
| rs12452511 | snp | A/G | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67836460 | GTATTTCAGAAATGC[A/G]TGTATTAATCTGTGT | 2186 |
| rs12452570 | snp | C/T | 0.220246 | 0.248223 | intron-variant | BPTF | GRCh38.p7 | 17:67961898 | AGAATCGCTTGAACC[C/T]GGGAGACTGAGGTTG | 2186 |
| rs12452598 | snp | C/T | 0.220246 | 0.248223 | intron-variant | BPTF | GRCh38.p7 | 17:67962035 | ATAGCCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 2186 |
| rs12452823 | snp | A/G | 0.401215 | 0.199083 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67889667 | ACAAAAATTAGCTGG[A/G]CATGGTGGCGGGCGC | 2186 |
| rs12452871 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BPTF | GRCh38.p7 | 17:67890046 | CCATACCTTAAAAAT[C/T]GGGGCTGGAAATTTG | 2186 |
| rs12452966 | snp | A/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67877396 | CCAAACTCTGTTACC[A/C]CTGTTTACTACCTAT | 2186 |
| rs12453701 | snp | A/G | 0.204496 | 0.245824 | intron-variant | BPTF | GRCh38.p7 | 17:67968616 | ACCCCGTGTTAGCCC[A/G]TCTCTACTAAAAATA | 2186 |
| rs12453719 | snp | A/G | 0.204496 | 0.245824 | intron-variant | BPTF | GRCh38.p7 | 17:67968645 | TACAAAAAATTAGCC[A/G]GGTGTGGTGGCGGGC | 2186 |
| rs12453733 | snp | A/G | 0.204496 | 0.245824 | intron-variant | BPTF | GRCh38.p7 | 17:67968753 | AGATTGTGCCACTGC[A/G]CTCTAGCCTGGCTGA | 2186 |
| rs12600508 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67973038 | TAAAatatatatatt[A/T]atatatatatatatt | 2186 |
| rs12600941 | snp | A/G | 0.397271 | 0.202018 | intron-variant | BPTF | GRCh38.p7 | 17:67922691 | TCTTTGGCTGCTTTC[A/G]TGATACAAAGGCACA | 2186 |
| rs12601759 | snp | A/G | 0.431621 | 0.171796 | intron-variant | BPTF | GRCh38.p7 | 17:67959168 | CAGAGAGCAAGAGCA[A/G]CTAGAAGAAAGCAGC | 2186 |
| rs12601919 | snp | A/G | 0.417521 | 0.185571 | intron-variant | BPTF | GRCh38.p7 | 17:67829258 | CAGGCATTTTCCTTT[A/G]TTGGCTGTGATGTTA | 2186 |
| rs12601921 | snp | C/T | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67829238 | TGCTATTTCATATTG[C/T]TTGCCAGGCATTTTC | 2186 |
| rs12602211 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67972854 | ACCAAGAATGTCCTA[A/G]TGTGATGTGTGCGTT | 2186 |
| rs12602556 | snp | A/G | 0.417034 | 0.18601 | intron-variant | BPTF | GRCh38.p7 | 17:67830745 | AATAGGAAATAAACC[A/G]AAGCTCCTTTGTATG | 2186 |
| rs12602655 | snp | A/G | 0.397813 | 0.201621 | intron-variant | BPTF | GRCh38.p7 | 17:67913326 | GATAGTAATGGAAAC[A/G]GGATACAGAAAGCTT | 2186 |
| rs12602912 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67873957 | AATACAAGGTGAGCC[C/T]GGAGCATCTTGTAAT | 2186 |
| rs12603139 | snp | G/T | 0.375 | 0.216506 | intron-variant | BPTF | GRCh38.p7 | 17:67852956 | gcctagccaatatgg[G/T]gaaaccccatctcta | 2186 |
| rs12603589 | snp | C/T | 0.417521 | 0.185571 | intron-variant | BPTF | GRCh38.p7 | 17:67829132 | TGTTGTTGTTTTTTC[C/T]AATTGGTTTTTGATG | 2186 |
| rs12603649 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | BPTF | GRCh38.p7 | 17:67920279 | CCAAATTTTGAAAAT[A/G]ATATTAAAGTAATAA | 2186 |
| rs12936095 | snp | A/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67904129 | cgcctcctgggttca[A/C]acgattctcctgcct | 2186 |
| rs12936116 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67926164 | aggcatgcaccaccg[G/T]gtctggctgattttt | 2186 |
| rs12936366 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | BPTF | GRCh38.p7 | 17:67882329 | atgcttttttggtgg[G/T]tagtgttatgaaaga | 2186 |
| rs12937518 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67872206 | AATGTATATATGTAT[A/G]TGTGTATTTAACAAT | 2186 |
| rs12938158 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | BPTF | GRCh38.p7 | 17:67882436 | CTTTGTTTACATTTG[C/G/T]ATATCTGTTCCCTTA | 2186 |
| rs12938247 | snp | A/G | 0.221439 | 0.248363 | intron-variant | BPTF | GRCh38.p7 | 17:67967487 | CATTTCTTAGGATTT[A/G]catgtgcacaagtat | 2186 |
| rs12938254 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67872225 | GTATTTAACAATATA[G/T]ACTATTTGAAATTAG | 2186 |
| rs12938271 | snp | G/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67872240 | GACTATTTGAAATTA[G/T]AATCTTTATAGAAAG | 2186 |
| rs12938781 | snp | C/T | 0.221737 | 0.248397 | intron-variant | BPTF | GRCh38.p7 | 17:67967559 | tggcggggtggctca[C/T]gctggaatcccagca | 2186 |
| rs12938820 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67884369 | gatccgcccacctca[A/G]ccttccaaagtgttg | 2186 |
| rs12939100 | snp | C/T | 0.221737 | 0.248397 | intron-variant | BPTF | GRCh38.p7 | 17:67967674 | AAATAGAAAAATTAG[C/T]CAGTTGTGGTGGCAG | 2186 |
| rs12940964 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67930336 | ctcaagtagctggga[C/T]tacaggcacccacca | 2186 |
| rs12941483 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | BPTF | GRCh38.p7 | 17:67901098 | TTAGTGAAAAAGGTA[C/T]TAGATATTAAAGCAC | 2186 |
| rs12942081 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67923470 | GGTCCTCTCTCTCTG[G/T]Ctttttttttttttt | 2186 |
| rs12942774 | snp | A/G | 0.465788 | 0.126237 | intron-variant | BPTF | GRCh38.p7 | 17:67971446 | CACTGTGACACCTCC[A/G]CACTTCAGCATGGGC | 2186 |
| rs12942919 | snp | A/T | 0.220246 | 0.248223 | intron-variant | BPTF | GRCh38.p7 | 17:67962325 | CAGTCTGGTTCCCTG[A/T]GATTCATGGTAATTC | 2186 |
| rs12944451 | snp | A/T | | | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67897343 | tgaaactctgtctca[A/T]aaaaaaaaaaaaaaa | 2186 |
| rs12944942 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | BPTF | GRCh38.p7 | 17:67976730 | ATAAGAATAAAAGAA[A/G]AATTTCCTGAGCTGA | 2186 |
| rs12945266 | snp | C/T | 0.362732 | 0.22314 | upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67825365 | TGCCGAGCCCAGGCG[C/T]CCAGGGCTCCCCGCC | 2186 |
| rs12947253 | snp | G/T | 0.375 | 0.216506 | intron-variant | BPTF | GRCh38.p7 | 17:67881865 | GGGTTtttgtttttt[G/T]ttttttttttttttt | 2186 |
| rs12947658 | snp | A/G | 0.465996 | 0.12588 | intron-variant | BPTF | GRCh38.p7 | 17:67906890 | AAGTGAAGAAGGTAA[A/G]GAATAGGAAAATGCC | 2186 |
| rs12948730 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67953041 | tctcggctcactgca[A/G]gctccgtctccccgg | 2186 |
| rs12949469 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BPTF | GRCh38.p7 | 17:67953030 | cagtggcacgatctc[A/G]gctcactgcaagctc | 2186 |
| rs12950044 | snp | C/T | 0.203267 | 0.245593 | intron-variant | BPTF | GRCh38.p7 | 17:67968329 | ATGAAGTAGTTATTA[C/T]CTCTGTTCTCCTGAT | 2186 |
| rs12951123 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67953026 | agtgcagtggcacga[A/T]ctcggctcactgcaa | 2186 |
| rs12952034 | snp | A/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67926192 | tttgtgttttttgta[A/G]agataggacttttgc | 2186 |
| rs16961461 | snp | C/G | 0.0678174 | 0.1712 | intron-variant | BPTF | GRCh38.p7 | 17:67861922 | CCTGAACCCCTTTTT[C/G]TCTTGCATCGTGAAA | 2186 |
| rs28394423 | snp | A/G | | | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982562 | TATTGAAAAAAAAAG[A/G]AAAAGAAAGCAAGAA | 2186 |
| rs28457624 | snp | A/G | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67939055 | AGAGCTGGCAGTAGT[A/G]TGAATTGGAATAACC | 2186 |
| rs28541293 | snp | A/G | 0.0309521 | 0.120491 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982561 | TTATTGAAAAAAAAA[A/G]AAAAAGAAAGCAAGA | 2186 |
| rs28560431 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67835735 | CGGTGGCGCGATTTC[C/G]GCTCACTGTGAGCTC | 2186 |
| rs28575379 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67955981 | GGCAAAACCCTGTTT[C/T]TACAAAAAAGAATTC | 2186 |
| rs28599618 | snp | A/C | 0.21048 | 0.246857 | intron-variant, utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67981866 | TCATCAATGTAAATA[A/C]ACACACACACACACA | 2186 |
| rs28601724 | snp | A/T | 0.191775 | 0.243125 | intron-variant | BPTF | GRCh38.p7 | 17:67828312 | GCCGGTAATTGAAAC[A/T]CGGAGACTGAATTGC | 2186 |
| rs28609796 | snp | A/T | 0.419776 | 0.18351 | intron-variant | BPTF | GRCh38.p7 | 17:67858988 | CAGAGACCTGTAAAA[A/T]GAAGTAGTTGTGATA | 2186 |
| rs28631860 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67884146 | TTTCTTTCTTTTTTT[C/T]TTTTTTTTTTTGAAA | 2186 |
| rs28639534 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67835705 | GAGTCTCGCTCTGTC[C/G]CCCAGGCTGGAGTGC | 2186 |
| rs28677969 | snp | C/G | 0.131723 | 0.220251 | intron-variant | BPTF | GRCh38.p7 | 17:67896184 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT | 2186 |
| rs28805033 | snp | C/T | 0.161596 | 0.233848 | intron-variant | BPTF | GRCh38.p7 | 17:67844317 | CAGTGGCGCAATCTC[C/T]GCTCACTGCAAGCTC | 2186 |
| rs34000805 | in-del | -/T | 0.494272 | 0.053207 | intron-variant | BPTF | GRCh38.p7 | 17:67851920 | GTGAGATTGGGGTCC[-/T]TTTTTTTTTTTAATG | 2186 |
| rs34013890 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67915816 | GATTCTAGTTTACCT[-/G]CTGTGTCCCCAGCTC | 2186 |
| rs34028031 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67899527 | ACTTGATGCTGAGTT[C/T]TTTTTCTTTTTTTTT | 2186 |
| rs34038380 | snp | A/G | 0.0290449 | 0.116957 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67911162 | TTAAGGGTATAGGAA[A/G]GACTTCTACAAATTC | 2186 |
| rs34069377 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67964994 | AGAGTGTGAGACTCC[A/T]TCGCAAAAAAAAAAA | 2186 |
| rs34111057 | snp | A/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67894408 | GTCTCGGCTTGCTGT[A/G]ACCTCTGCCTCCCAT | 2186 |
| rs34128699 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67917247 | AGCTATTCTTCTTTC[-/T]TCAGCCTCCCAACTA | 2186 |
| rs34143014 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67826580 | TCGCTCGCTCTCTCT[-/C]CCCCCCCCCAACCCC | 2186 |
| rs34219218 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67831284 | GAATGGTAGCACTTT[-/C]CAGTAACAATGGGGA | 2186 |
| rs34261763 | in-del | -/TGGA | | | intron-variant | BPTF | GRCh38.p7 | 17:67873993 | AAAGTAAGAAAATGC[-/TGGA]TGGATGGATGGATGG | 2186 |
| rs34281279 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67864526 | GAGTGAGACTCCATC[A/T]CAAAAAAAAAAAAAA | 2186 |
| rs34347759 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67867019 | TATATCTAAACATTT[-/A]AAAAAGGTAATACGT | 2186 |
| rs34359683 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67915843 | CTCCTTTCACATAGT[-/G]CTAACACATAGAAGA | 2186 |
| rs34373506 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67913903 | GGCTACAGAGACACA[-/G]GGAATAGTGCCCGGT | 2186 |
| rs34377471 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67964068 | AAATTAATGAACTGG[-/G]AATGTCAATCTTGAA | 2186 |
| rs34389001 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67948035 | TGTCTTAAGCCTTTC[-/A]AAAATGAAACGCCCA | 2186 |
| rs34432450 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | BPTF | GRCh38.p7 | 17:67884143 | CATTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTG | 2186 |
| rs34482518 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67873125 | AGGAAACACAAACCC[-/A]AAAATCCAAGAGGAG | 2186 |
| rs34498187 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67843710 | TGGGTGTGAGGGTGG[-/T]TCTTTTGTGATAATG | 2186 |
| rs34520139 | in-del | -/A | 0.347253 | 0.230308 | intron-variant | BPTF | GRCh38.p7 | 17:67907185 | CAAGACACTGTCTCC[-/A]AAAAAAAAAAAAAAA | 2186 |
| rs34530035 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67968750 | CAAGATTGTGCCACT[-/A]GCACTCTAGCCTGGC | 2186 |
| rs34537462 | in-del | -/T | 0.461259 | 0.133677 | intron-variant | BPTF | GRCh38.p7 | 17:67908510 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 2186 |
| rs34541347 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67947676 | TTATCTGTGTACTAA[-/C]CCTGTGGTGATTATA | 2186 |
| rs34567645 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67843106 | ATATATCTATATATA[-/T]TGTAGATGTATGTAG | 2186 |
| rs34623030 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67931189 | GAATTGCTTGAACCC[-/G]GGGAGGCGGAGGTTG | 2186 |
| rs34629375 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67919529 | GATAACAGAGCAAAA[-/C]CCCTGTCTCTTAAAA | 2186 |
| rs34656215 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67914402 | CAATAGAGACAGCTG[-/A]AAAAGTACAATTTCT | 2186 |
| rs34662658 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67905075 | CTTGTTTTTTAGAAG[-/C]ACGCCTCAGCCGCCT | 2186 |
| rs34675073 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67925081 | TTTTTTTAAGTGTAT[-/A]CTCACGTCTATCTTA | 2186 |
| rs34733047 | in-del | -/A | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67852002 | ATTGATAATGAGTGT[-/A]AATGCTCAGTGGCAT | 2186 |
| rs34739687 | in-del | -/A | 0.494484 | 0.0522255 | intron-variant | BPTF | GRCh38.p7 | 17:67865999 | GTGGCACATGTCTGT[-/A]AGTCCTAACTACTTG | 2186 |
| rs34746180 | in-del | -/AG/GTGT/GTGTA/T/TGT | | | intron-variant | BPTF | GRCh38.p7 | 17:67944925 | GGGGACAGCCAAGAA[-/AG/GTGT/GTGTA/T/TGT]GCAGGGCCCAGGCTT | 2186 |
| rs34791362 | in-del | -/A/C | | | intron-variant, utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67981869 | CAATGTAAATAAACA[-/A/C]ACACACACACACACA | 2186 |
| rs34791938 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67974689 | ACCAGTTTCTCAAGG[-/G]ACACTGCAAAGGATT | 2186 |
| rs34859839 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67901832 | CTATATCCGTCAGCA[-/T]TTTTCAGTGCAAGAA | 2186 |
| rs34867919 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67932911 | AATTCAATGTTTAAT[-/A]AAAAGGAAAAATTTA | 2186 |
| rs34872586 | snp | C/T | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67867350 | TTAAAAAAATAAAAC[C/T]TTAAATTTTAGAGTA | 2186 |
| rs34914957 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67859359 | TGTGTTGGCCAGGCT[-/G]GGTCTCAAACTCCTG | 2186 |
| rs34923633 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67960834 | TTGAAGCTGCTTTGG[-/G]TGGTGCTATCTAAAT | 2186 |
| rs34934455 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67908827 | AGTTGTCACTGACAA[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs34938697 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67906375 | GACCACTGCGCCTGG[-/C]CCTATAAATAAGCTA | 2186 |
| rs34955199 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | BPTF | GRCh38.p7 | 17:67868957 | GTATTTCTCTATTAG[A/C]TCTGTTTAGAAAAAT | 2186 |
| rs35046479 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67858070 | GGATTACAGGCGTGA[-/G]CGACCGTGCCCGGCT | 2186 |
| rs35078759 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67936235 | TGTTTTAAGGCAATC[-/A]GTCTTGCCTAAGTAG | 2186 |
| rs35126595 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67920043 | GAAATCACAACAACA[-/G]GAAATAATTAAGAGG | 2186 |
| rs35146367 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67835212 | CTCTTAAAAAAAAAA[-/A]TTTAAGTAAAATGAA | 2186 |
| rs35161459 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67939871 | GCGACAGAGCGAGAC[-/T]TCCGTCTCAAAAAAA | 2186 |
| rs35169238 | in-del | -/T | 0.480223 | 0.0974544 | intron-variant | BPTF | GRCh38.p7 | 17:67827931 | ACTTAATTTTAGTAC[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs35187423 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67932593 | TAATCCCAGCTACTT[-/G]GGGAGGCCGAGGTGG | 2186 |
| rs35204647 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67942019 | AAAAAGACAAACAGG[-/C]CAAGGTGCGGTGGCT | 2186 |
| rs35220893 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67826802 | ATCTGTTACTTAAAA[-/A]GGGAATTAAGGATTT | 2186 |
| rs35234780 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67895333 | GCAAGACTTCATCTC[-/A]AAAAAAAAAAAAAAA | 2186 |
| rs35243555 | snp | C/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67880361 | CTAGCTTCTGAAGAT[C/G]GTTGCTTTGATGGTT | 2186 |
| rs35306191 | in-del | -/CT/TC | | | intron-variant | BPTF | GRCh38.p7 | 17:67852462 | ATCCCCTTGCCCTCC[-/CT/TC]TTTTTATTTTTAGTT | 2186 |
| rs35318571 | snp | A/G | 0.375 | 0.216506 | intron-variant | BPTF | GRCh38.p7 | 17:67973067 | TTTTATATATATATA[A/G]ATATATATATAATAT | 2186 |
| rs35407119 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67844071 | TGCCCGGCCCCCGCC[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs35420192 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67894928 | CTACTTTTTAGCCCT[-/G]GATAGACTTGCTTTG | 2186 |
| rs35424987 | in-del | -/C | | | frameshift-variant | BPTF | GRCh38.p7 | 17:67945543 | CAGCCTTCAGCTCAG[-/C]CCCAGCCCCAAACCC | 2186 |
| rs35427238 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67858072 | GATTACAGGCGTGAC[C/G]ACCGTGCCCGGCTAA | 2186 |
| rs35438304 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67867121 | GTATATTTTACTTTA[-/G]GTTCTCCATATTTCA | 2186 |
| rs35445764 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67855951 | GTGTTCTGCAGTTTT[-/C]ACAGTGATACGCCCT | 2186 |
| rs35456363 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BPTF | GRCh38.p7 | 17:67956945 | CTCCAGCCTGGGAGA[C/T]AGAGCGAGACTCCGT | 2186 |
| rs35606762 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67931690 | TTGGTATCAGTGGCA[-/G]GGGAATTTTGTATGA | 2186 |
| rs35655994 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67894235 | TAGCCTATTAATAAT[-/G]GAAAGTTAATATATT | 2186 |
| rs35665944 | snp | G/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67959524 | GATAGTCTTGTATTG[G/T]CTTTAATTGACAACA | 2186 |
| rs35702319 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67918203 | GCCTCCCACAGTGCT[-/G]GGGATTACAGGCGTG | 2186 |
| rs35711041 | snp | A/G | 0.0329466 | 0.124048 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67826294 | CGCCAGTTACTGCAC[A/G]GAAAGCAGCTTCAGG | 2186 |
| rs35727338 | in-del | -/TT | | | intron-variant | BPTF | GRCh38.p7 | 17:67857148 | GTTCGTCTTTAACAA[-/TT]TTTTTTTTTTTTTTT | 2186 |
| rs35767527 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67946988 | GAGTTTGAATGTGGA[-/T]TTTTAAGTGTTACCA | 2186 |
| rs35770209 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67912575 | ATGACTTTATTGATG[-/A]AAATGGTCTGCCCAT | 2186 |
| rs35827193 | in-del | -/T | 0.454423 | 0.143914 | intron-variant | BPTF | GRCh38.p7 | 17:67909280 | AGGTCCCCCCCCCCC[-/T]TTTTTTTTTTATCCT | 2186 |
| rs35912904 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67931695 | ATCAGTGGCAGGGAA[-/T]TTTTGTATGATAGCA | 2186 |
| rs35916512 | multinucleotide-polymorphism | CT/GG | | | intron-variant | BPTF | GRCh38.p7 | 17:67894413 | GGCTTGCTGTAACCT[CT/GG]GCCTCCCATATTCAA | 2186 |
| rs35935942 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67942063 | CAGCACTTTGGGGGG[-/C]CCAAGGTTTTGGGAG | 2186 |
| rs35937223 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67872427 | ATGTAGTTGTGTTTG[-/A]AAATGGCCGGGCGTG | 2186 |
| rs35999365 | in-del | -/TTT | | | intron-variant | BPTF | GRCh38.p7 | 17:67857802 | TTTTTTTTTTTTTTT[-/TTT]GAGACAGCGTCTCAC | 2186 |
| rs36046179 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67926041 | ACAAGGTCTCACTCT[C/T]TTGCCCAGGCTGCTG | 2186 |
| rs36066406 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67890662 | TTAAAGTGTGGGAGG[C/G]CGGTGGTGAGGGAAG | 2186 |
| rs36098432 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67880886 | ACTCTTGTTTTGTGG[-/C]CCCAACATTTAATTA | 2186 |
| rs36112553 | in-del | -/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67850950 | TAAATGGCAATGCAG[-/C]ATATAATAAACAAAT | 2186 |
| rs41411248 | snp | A/C/G/T | 0.18 | 0.24 | intron-variant | BPTF | GRCh38.p7 | 17:67830950 | CAAATCACAGAGATG[A/C/G/T]TGTTGAACCACTGGT | 2186 |
| rs55639539 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | BPTF | GRCh38.p7 | 17:67965365 | AAAGAAAAACGGGAT[C/T]GAGATGGTTTGCAGG | 2186 |
| rs55691924 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67898942 | AAAAAAAAAAAAAAA[-/A]TTTCTAAAAGTACCA | 2186 |
| rs55739716 | snp | C/T | 0.193653 | 0.243567 | intron-variant | BPTF | GRCh38.p7 | 17:67880956 | TGTATATTATATATA[C/T]ATACACACACACACA | 2186 |
| rs55788577 | snp | A/G | 0.15698 | 0.23205 | intron-variant | BPTF | GRCh38.p7 | 17:67833211 | ATGTATCAGTACTAT[A/G]TTTGAATAACACTTC | 2186 |
| rs55829095 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67978308 | TATATATATATATAT[A/T]TTTTTTTTGAGACAG | 2186 |
| rs55851004 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67971775 | TTGCGTTGCAGTGAT[C/T]TGAGATCATGCCACT | 2186 |
| rs55890520 | in-del | -/CAAGA | | | intron-variant | BPTF | GRCh38.p7 | 17:67976720 | AAAAAAAAAATAAGA[-/CAAGA]ATAAAAGAAGAATTT | 2186 |
| rs55896768 | snp | C/T | 0.49621 | 0.0433651 | intron-variant | BPTF | GRCh38.p7 | 17:67917242 | GGTTCGAGCTATTCT[C/T]CTTTCTCAGCCTCCC | 2186 |
| rs55931203 | snp | C/T | 0.395453 | 0.203331 | intron-variant | BPTF | GRCh38.p7 | 17:67858486 | CTTGAACCTAGGAGG[C/T]GGAGGTTGCAATGAG | 2186 |
| rs55939964 | snp | A/G | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67873181 | TGTTTCTTATGGCCC[A/G]GTGCAGTGGCTCACG | 2186 |
| rs55977218 | snp | A/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67858281 | TTTTCTTGCTCCCTT[A/C]CCTCCCAAACATCTG | 2186 |
| rs56009241 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67926798 | GCTGGAGTGTAGTGG[C/T]GAGATCATAGCTCAT | 2186 |
| rs56011159 | snp | C/G/T | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67838073 | CAAACTTGTTCTTAG[C/G/T]TTACCAATTAGTAGA | 2186 |
| rs56036698 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67914836 | ATTACTTGATTTCAC[A/C]TTTTTTAATGGGAGG | 2186 |
| rs56092143 | snp | A/G/T | 0.0252325 | 0.109451 | intron-variant | BPTF | GRCh38.p7 | 17:67976302 | ACATGGGGAAACCCC[A/G/T]TCTCTACCAAAAATA | 2186 |
| rs56099409 | in-del | -/AA/AAA | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67952077 | AAAAAAAAAAAAAAA[-/AA/AAA]TTATTGCTAAGGTAA | 2186 |
| rs56127116 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BPTF | GRCh38.p7 | 17:67885918 | GTCCTCACCCCCCCA[A/G]AAAAAGTCAGTGAGT | 2186 |
| rs56131244 | in-del | -/T | 0.215747 | 0.247642 | intron-variant | BPTF | GRCh38.p7 | 17:67952266 | TTTTTTTTAATAGGC[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs56148300 | snp | C/T | 0.49621 | 0.0433651 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896636 | TATTGTTTAGGGATA[C/T]AGACGTTTGTAAAAT | 2186 |
| rs56157608 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | BPTF | GRCh38.p7 | 17:67904283 | GATCCTCCTGACTTG[A/G]CCTCCCAAAGTGCTG | 2186 |
| rs56181830 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67928248 | TACTTCAGAAATGTA[A/G]TGGAATTTCTTAAGG | 2186 |
| rs56320024 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67917194 | GTGGAGTGCAGTGGA[A/G]CGATCTCGGCTCACT | 2186 |
| rs56321665 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67976716 | AAAAAAAAAAAAAAA[C/T]AAGAATAAAAGAAGA | 2186 |
| rs56335701 | in-del | -/TTTTTTTTTT | | | intron-variant | BPTF | GRCh38.p7 | 17:67843773 | TTTTTTTTTTTTTTT[-/TTTTTTTTTT]GAGATGGAGTTTTGC | 2186 |
| rs56340249 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67869824 | CCGTCTCTACTAAAA[A/T]TACAAAAAAAAAAAA | 2186 |
| rs56358780 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67976652 | GATTACACCACTGCT[C/T]TCCAACCTGAGTGAC | 2186 |
| rs56362274 | snp | C/G | 0.137867 | 0.223442 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896724 | TACTCAACTATAAAT[C/G]ATAAAACTAGAAGAC | 2186 |
| rs56393562 | snp | C/T | 0.431473 | 0.171952 | intron-variant | BPTF | GRCh38.p7 | 17:67937802 | TTATCCCTCTTCCTA[C/T]GCCACACTAGCTTTT | 2186 |
| rs56404791 | snp | G/T | 0.49614 | 0.0437598 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896903 | ACCAACCTAAAGAAA[G/T]AAAATATTAAAGATG | 2186 |
| rs56665640 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67830749 | GGAAATAAACCAAAG[C/T]TCCTTTGTATGCTGT | 2186 |
| rs56934829 | snp | A/T | 0.479824 | 0.098392 | intron-variant | BPTF | GRCh38.p7 | 17:67978306 | TATATATATATATAT[A/T]TATTTTTTTTGAGAC | 2186 |
| rs57065333 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | BPTF | GRCh38.p7 | 17:67953721 | GCTGGGATTACAGGC[A/G]TGCACCACCATGCCC | 2186 |
| rs57189261 | in-del | -/TGTA | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67944926 | GGGACAGCCAAGAAG[-/TGTA]CAGGGCCCAGGCTTC | 2186 |
| rs57247614 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67960786 | ATTCCTAAAATAAAA[A/C/T]TGTGGTCCCTTTAAT | 2186 |
| rs57310551 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67953274 | CTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTAC | 2186 |
| rs57367735 | in-del | -/AA | | | intron-variant | BPTF | GRCh38.p7 | 17:67930133 | AAAAAAAAAAAAAAA[-/AA]TTAAAAAGTAATCTA | 2186 |
| rs57373284 | snp | A/G | 0.185603 | 0.241564 | intron-variant | BPTF | GRCh38.p7 | 17:67964727 | TGTTCTTGGCCGGGC[A/G]TGGTGGCTCATGCCT | 2186 |
| rs57420634 | snp | A/G | 0.228547 | 0.249078 | intron-variant | BPTF | GRCh38.p7 | 17:67964783 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCAG | 2186 |
| rs57586285 | in-del | -/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67858620 | GGAAATTCAGTGATG[-/G]CTGCCTGTCAGGGAG | 2186 |
| rs57635853 | snp | A/C | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67880772 | TTCCTAAGTAGCTGA[A/C]ACTATAGGCTAATTA | 2186 |
| rs57831909 | snp | C/T | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67937202 | AGCTCACGCCTAATA[C/T]ACCAGCACTTTGGGA | 2186 |
| rs57870932 | in-del | -/ACAC | | | intron-variant | BPTF | GRCh38.p7 | 17:67880980 | CACACACACACACAC[-/ACAC]GTATATATATTACAT | 2186 |
| rs57922690 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | BPTF | GRCh38.p7 | 17:67880160 | ATTTTTCCAATCTGG[A/T]AATTCGTTACCTGCC | 2186 |
| rs57947185 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67837425 | TTGTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 2186 |
| rs57971998 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67851290 | TTTTTTTTTTTTTTT[-/T]AATAACCACCATATA | 2186 |
| rs58009257 | in-del | -/A | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67965020 | AAAAAAAAAAAAAAA[-/A]GATTATAGTTATTCT | 2186 |
| rs58069778 | snp | A/G | 0.181659 | 0.240478 | intron-variant | BPTF | GRCh38.p7 | 17:67896108 | ACTGGGACTATAGGC[A/G]CCCACCACTATGCCC | 2186 |
| rs58071304 | in-del | -/TA | | | intron-variant, downstream-variant-500B | BPTF | GRCh38.p7 | 17:67919215 | TAATAATAATAATAA[-/TA]ATAAAATATAATGCT | 2186 |
| rs58086300 | snp | A/T | | | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67984302 | TAACAAATTGTGGCA[A/T]ATTCTAAACAGCAAT | 2186 |
| rs58122682 | snp | C/T | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67880799 | ATTATCTTTTTTTTT[C/T]CTAGTTGATTTCTAG | 2186 |
| rs58141639 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67868786 | CCAACCTTGTTCTCA[C/T]ATATTCTACATCAAT | 2186 |
| rs58143986 | in-del | -/AA | | | intron-variant | BPTF | GRCh38.p7 | 17:67967830 | CAAAAAAAAAAAAAA[-/AA]GATTGGAAATGAAAT | 2186 |
| rs58204525 | snp | A/G | 0.0127156 | 0.0787154 | intron-variant | BPTF | GRCh38.p7 | 17:67932067 | CTCAACAGCCAGTCT[A/G]GGAAATACGTAATTC | 2186 |
| rs58205471 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67879153 | TTTTTTTTTTTTTTT[-/T]CTTTTTGAGATGGAG | 2186 |
| rs58224652 | snp | C/T | 0.198944 | 0.244731 | intron-variant | BPTF | GRCh38.p7 | 17:67880958 | TATATTATATATATA[C/T]ACACACACACACACA | 2186 |
| rs58342878 | in-del | -/ATTGTC | | | intron-variant | BPTF | GRCh38.p7 | 17:67917130 | TAATATGGTATTGTC[-/ATTGTC]CTTTTTTTTTTTTTT | 2186 |
| rs58396713 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | BPTF | GRCh38.p7 | 17:67856673 | AGCTCTAGAGGAGCA[A/G]TGGCATGGAAGGGCC | 2186 |
| rs58427954 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | BPTF | GRCh38.p7 | 17:67949482 | TGGGATGCTGAGGCA[G/T]GATAATCGTTTGAAC | 2186 |
| rs58462646 | in-del | -/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67923500 | TTTTTTTTTTTTTTT[-/T]GAAGCAGAGTCTCGC | 2186 |
| rs58551145 | snp | A/G | 0.40157 | 0.198813 | intron-variant | BPTF | GRCh38.p7 | 17:67841119 | TTGGTAAAAGGTCAG[A/G]TAGTAAGGCCAGGCA | 2186 |
| rs58619607 | in-del | -/GA | | | intron-variant | BPTF | GRCh38.p7 | 17:67949682 | ATATATATACACACA[-/GA]CATACATATATATAT | 2186 |
| rs58715849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67937348 | TGTAATCCCAGCTAC[G/T]CGGGAGGCTGAGGCA | 2186 |
| rs58768748 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BPTF | GRCh38.p7 | 17:67916782 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGCATTGCC | 2186 |
| rs58830404 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67840485 | GTTGCTGCTGCTGCT[C/G]CTCCTCCGCCTCCTC | 2186 |
| rs58841746 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67971844 | AAAAAAAAAAAAAAA[-/A]GAGAAGAAAAAAATT | 2186 |
| rs58842890 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67899819 | CAAGCATGAGCCACC[A/G]CGCCCGGCCTATGCT | 2186 |
| rs58991615 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67898942 | AAAAAAAAAAAAAAA[-/A]TTTCTAAAAGTACCA | 2186 |
| rs58996431 | snp | A/G | 0.0132963 | 0.0804449 | intron-variant | BPTF | GRCh38.p7 | 17:67922817 | GCAATATTGCTTAAA[A/G]TATTCTGATTTCCTT | 2186 |
| rs59023379 | snp | A/G | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67949623 | TATATACACACACAC[A/G]TATATACACATACGT | 2186 |
| rs59037558 | in-del | -/A | 0.0562307 | 0.157967 | intron-variant | BPTF | GRCh38.p7 | 17:67942324 | AAAAAAAAGAAAAAC[-/A]AAAAAAAAAGGACAA | 2186 |
| rs59056539 | in-del | -/TTT | | | intron-variant | BPTF | GRCh38.p7 | 17:67925071 | TTTTTTTTTTTTTTT[-/TTT]AAGTGTATCTCACGT | 2186 |
| rs59088743 | snp | A/G | 0.0127511 | 0.0788222 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67922976 | ATTGTGGGAGATCAG[A/G]GCATTTGCTGAGAGG | 2186 |
| rs59123759 | snp | G/T | 0.133093 | 0.220981 | intron-variant | BPTF | GRCh38.p7 | 17:67840493 | TGCTGCTGCTCCTCC[G/T]CCTCCTCCTTCCCCT | 2186 |
| rs59168608 | in-del | -/TC | | | intron-variant | BPTF | GRCh38.p7 | 17:67878703 | GTGTGTGTGTGTGTG[-/TC]AGTCGTTTAGATATC | 2186 |
| rs59187095 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67869852 | AAAAAAAAAAAAAAA[A/T]TTAGCCAGGCGTGGT | 2186 |
| rs59252707 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67840471 | CTCTTGTTGTTGTTG[C/T]TGCTGCTGCTGCTGC | 2186 |
| rs59260443 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | BPTF | GRCh38.p7 | 17:67843225 | GTATGTAGATATATA[C/T]CTATATATCTACATA | 2186 |
| rs59327152 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67870026 | AAAAAAAAAAAAAAA[-/A]TTAGCAAAACCTTTT | 2186 |
| rs59480488 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | BPTF | GRCh38.p7 | 17:67931329 | GAATGAATGATTAGC[C/T]GGACATGGTGCCATT | 2186 |
| rs59543153 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67961972 | GAGCAAAGCTCTGTC[-/A]AAAAAAAAAAAGAAA | 2186 |
| rs59583423 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | BPTF | GRCh38.p7 | 17:67921530 | GACTCCATTTCCAAG[C/T]AAATAAATAAATAAA | 2186 |
| rs59596149 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67922042 | TCTCCAAAAAAAAAA[A/C]AAAATCACAAGGTCG | 2186 |
| rs59606889 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67827728 | GGAGAAGTAGGGTAG[C/T]ATTAAGCCAAATGTG | 2186 |
| rs59640213 | snp | A/G | 0.496714 | 0.0404017 | intron-variant | BPTF | GRCh38.p7 | 17:67896164 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 2186 |
| rs59700705 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BPTF | GRCh38.p7 | 17:67839337 | CTAAGTTTTTTTTTA[A/T]AAAAAAATCAGCTAT | 2186 |
| rs59729944 | in-del | -/GA | | | intron-variant | BPTF | GRCh38.p7 | 17:67963717 | TGAGACACATTGGGG[-/GA]AAAATGTGGTTTAAT | 2186 |
| rs59839937 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67933952 | GGGAGGCTGAGGCAA[A/G]AGAATTGCTCGAACT | 2186 |
| rs59848297 | snp | A/G | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67907417 | CTAGAGTGCAGTGGC[A/G]TGGTCTCAGCTCACT | 2186 |
| rs59854755 | snp | A/G/T | 0.227664 | 0.249 | intron-variant | BPTF | GRCh38.p7 | 17:67858688 | GCAGGTCACGTTCAC[A/G/T]CAGTCTCAAGTGCCC | 2186 |
| rs59862562 | in-del | -/GATATATA | | | intron-variant | BPTF | GRCh38.p7 | 17:67843224 | GTATGTAGATATATA[-/GATATATA]CCTATATATCTACAT | 2186 |
| rs59876337 | snp | A/T | 0.191775 | 0.243125 | intron-variant | BPTF | GRCh38.p7 | 17:67827670 | GGTAGTAGAAGTGGT[A/T]AACTTGAAAAGTTTG | 2186 |
| rs59916565 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67906330 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 2186 |
| rs59948838 | snp | C/T | 0.19334 | 0.243495 | intron-variant | BPTF | GRCh38.p7 | 17:67917714 | CTTGGCTCACTGCAG[C/T]CTCTGCCTCCTGGGT | 2186 |
| rs59950564 | snp | A/G | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67864743 | AATGCTGTGGATCAG[A/G]AGTATTATGGGCTTT | 2186 |
| rs59956089 | snp | C/T | 0.437824 | 0.164991 | intron-variant | BPTF | GRCh38.p7 | 17:67964738 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 2186 |
| rs60028468 | in-del | -/AT | | | intron-variant, utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982023 | TATATATATATATAT[-/AT]TTAAATATTGGCTTT | 2186 |
| rs60083535 | in-del | -/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67926022 | TTTTTTTTTTTTTTT[-/T]GAGACAAGGTCTCAC | 2186 |
| rs60083543 | snp | A/G/T | 0.219947 | 0.248187 | intron-variant | BPTF | GRCh38.p7 | 17:67944925 | AGGGGACAGCCAAGA[A/G/T]GCAGGGCCCAGGCTT | 2186 |
| rs60085248 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67842839 | AAAAAAAAAAAAAAA[-/A]GACATTTCAGATGAA | 2186 |
| rs60203396 | in-del | -/AC/ACAC/ACACAC/ACACACACACACAC | 0.625 | 0.125 | intron-variant, utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67981904 | CACACACACACACAC[lengthTooLong]CTTTCACCACAATGG | 2186 |
| rs60254895 | in-del | -/T | | | intron-variant, downstream-variant-500B | BPTF | GRCh38.p7 | 17:67919218 | TAATAATAATAATAA[-/T]AAAATATAATGCTTG | 2186 |
| rs60272759 | in-del | -/AAA | | | intron-variant | BPTF | GRCh38.p7 | 17:67864543 | AAAAAAAAAAAAAAA[-/AAA]GGAAAAGAAAAAAGT | 2186 |
| rs60308393 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67860579 | TCATTCATTATGTAA[G/T]TGGGCCAATCTTTCT | 2186 |
| rs60308484 | in-del | -/CCTTCACCTCCC/G/GCC/GCCCCTCCA/GCCCCTCCAGCCCCTCCC/GCCCCTCCC | 1.69249e-05 | 0.00290898 | cds-indel, frameshift-variant | BPTF | GRCh38.p7 | 17:67959666 | CCTCCAGCCCCTCCA[lengthTooLong]CCTTCACCTCCCCCT | 2186 |
| rs60432162 | in-del | -/T | 0.495708 | 0.0461266 | intron-variant | BPTF | GRCh38.p7 | 17:67884422 | CCCCTGGCCCCTCCC[-/T]TTTTTTTTTTTCTGA | 2186 |
| rs60432293 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67864291 | AGCACTTTGGGGAGG[C/T]TGAGGCGGGCGGATT | 2186 |
| rs60456082 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | BPTF | GRCh38.p7 | 17:67981115 | AGTGAGCTGTGATTG[C/T]GCCACTGCACTCCAG | 2186 |
| rs60463665 | snp | C/T | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67857722 | TCTGCCCTTCTCGGC[C/T]TCTCAAAGTGCTGGG | 2186 |
| rs60477798 | snp | A/C | 0.332106 | 0.236133 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67897174 | TCTACTTAAAAAAAA[A/C]AAAAACAAAAAACGA | 2186 |
| rs60507268 | in-del | -/AAAAAAAAAAAA | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67955293 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]GCTTCCTGAGGTACT | 2186 |
| rs60618921 | snp | A/G | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67936233 | TTTTGTTTTAAGGCA[A/G]TCGTCTTGCCTAAGT | 2186 |
| rs60626066 | snp | A/G | 0.37138 | 0.218556 | intron-variant | BPTF | GRCh38.p7 | 17:67965117 | GAGGCTGAGGCGGGT[A/G]GATCACAAGGTCAGG | 2186 |
| rs60707445 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67921235 | AAAAAAAAAAAAAAA[-/A]GAAATACAGGCCAGG | 2186 |
| rs60751133 | in-del | -/TT | | | intron-variant | BPTF | GRCh38.p7 | 17:67832805 | TTTTTTTTTTTTTTT[-/TT]GAGGCAGAGTCTCGC | 2186 |
| rs60762605 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67888193 | TATAATGCAAAGATT[-/T]CACCCACAACTTAAA | 2186 |
| rs60856912 | snp | G/T | 0.491783 | 0.0635686 | intron-variant | BPTF | GRCh38.p7 | 17:67896227 | TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 2186 |
| rs60968971 | in-del | -/TTTTTTTTTTTT | | | intron-variant | BPTF | GRCh38.p7 | 17:67857162 | AATTTTTTTTTTTTT[-/TTTTTTTTTTTT]GAGACAGAGTCTTGC | 2186 |
| rs61024674 | snp | A/T | 0.193028 | 0.243422 | intron-variant | BPTF | GRCh38.p7 | 17:67839335 | TCCTAAGTTTTTTTT[A/T]AAAAAAAAATCAGCT | 2186 |
| rs61067468 | snp | A/G | 0.401215 | 0.199083 | intron-variant | BPTF | GRCh38.p7 | 17:67869919 | AGGCAAGAGAATGGC[A/G]TGAACCCGGGAGGCA | 2186 |
| rs61116894 | in-del | -/A | | | intron-variant | BPTF | GRCh38.p7 | 17:67907201 | AAAAAAAAAAAAAAA[-/A]CCTTTAAGTCCCAAG | 2186 |
| rs61171763 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | BPTF | GRCh38.p7 | 17:67940893 | CTTTTAAACACCAAA[A/C]TTTTATTAGTTGGCT | 2186 |
| rs61184134 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | BPTF | GRCh38.p7 | 17:67967437 | GTGAGCCACCATACC[C/T]GGCCAATTGTGCATA | 2186 |
| rs61297499 | snp | A/G | 0.153 | 0.230415 | intron-variant | BPTF | GRCh38.p7 | 17:67919486 | TTCAAGGTTGCAGTG[A/G]CTGTGGTCCACTAAT | 2186 |
| rs61403085 | in-del | -/T | 0.375 | 0.216506 | intron-variant | BPTF | GRCh38.p7 | 17:67960346 | TATTTTAAGCAGTTG[-/T]TTTTTTTTGTATTAA | 2186 |
| rs61427510 | in-del | -/GT | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67878682 | CGTCTTTATGTGTTC[-/GT]GTGTGTGTGTGTGTG | 2186 |
| rs61482133 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | BPTF | GRCh38.p7 | 17:67964796 | ACAAGGTCAGGAGAT[C/G]AGACCATCCTGGCTA | 2186 |
| rs61489754 | in-del | -/A | 0.178465 | 0.239547 | intron-variant | BPTF | GRCh38.p7 | 17:67976073 | ACCTTAAATATCTTT[-/A]AAAAAAAAATAAATA | 2186 |
| rs61516059 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | BPTF | GRCh38.p7 | 17:67920722 | ATGTGTTGCAGTAAG[A/C]TAAGAGAGTAATATT | 2186 |
| rs61594807 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BPTF | GRCh38.p7 | 17:67844982 | TTCCAACCTCAAGTA[A/G]TCCATCCGCCTCAGC | 2186 |
| rs61665176 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | BPTF | GRCh38.p7 | 17:67975251 | TTTCCCTTACATTTA[A/C]GTGGACACTTATCAA | 2186 |
| rs61676547 | snp | C/G | 0.494526 | 0.0520291 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896391 | AAACATTTGGAGAGG[C/G]TGGGAGGGGCACAAG | 2186 |
| rs61682820 | in-del | -/T | 0.409891 | 0.192184 | intron-variant | BPTF | GRCh38.p7 | 17:67953575 | TTTTTTTTTTTTTTT[-/T]GGAGAAAGAGTTTTG | 2186 |
| rs61700018 | snp | A/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67921629 | ATGTATACAATTAAT[A/T]TTTGAAACTTGATTA | 2186 |
| rs62084208 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67831327 | AAGGGAAATTAATGA[C/T]ATCTGTTTTCAGTTA | 2186 |
| rs62084209 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67832253 | CAGCATGTTTCTTAA[A/T]TTAAAAAAAAAAAAC | 2186 |
| rs62084210 | snp | A/G | 0.416871 | 0.186156 | intron-variant | BPTF | GRCh38.p7 | 17:67832594 | AATGTACCCTTGTAA[A/G]GTATATAATTTAGTG | 2186 |
| rs62084212 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67844128 | TCTGTCACCCAGGCC[A/G]GAGTGCAGTGGCATG | 2186 |
| rs62084213 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67845900 | TAGGAATGTTTACCA[A/G]ACTATCCTAGAGCCA | 2186 |
| rs62084214 | snp | C/G | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67847209 | TACTTAGCACAATGT[C/G]TGGCAAATAGAAAGC | 2186 |
| rs62084215 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67850506 | CCCAAGTAGCTGGGA[A/G]TACAGGTGTGTGCCA | 2186 |
| rs62084234 | snp | A/G | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67850944 | TCCCATGTAAATGGC[A/G]ATGCAGATATAATAA | 2186 |
| rs62084235 | snp | C/T | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67857321 | GCCCGCCACCGTGCC[C/T]GGTTAATTTTTTGTA | 2186 |
| rs62084236 | snp | C/T | 0.0898934 | 0.192005 | intron-variant | BPTF | GRCh38.p7 | 17:67858619 | GTGGAAATTCAGTGA[C/T]GCTGCCTGTCAGGGA | 2186 |
| rs62084237 | snp | A/G | 0.393065 | 0.205018 | intron-variant | BPTF | GRCh38.p7 | 17:67858691 | GGTCACGTTCACGCA[A/G]TCTCAAGTGCCCTCC | 2186 |
| rs62084238 | snp | A/T | 0.417521 | 0.185571 | intron-variant | BPTF | GRCh38.p7 | 17:67860457 | CTTAAAAATATGTTA[A/T]TTGTATAGATTAGTG | 2186 |
| rs62084239 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | BPTF | GRCh38.p7 | 17:67862233 | CACCTGCCTCGGACT[C/T]CGAAAGTGCTGGGAT | 2186 |
| rs62084240 | snp | A/C | 0.40157 | 0.198813 | intron-variant | BPTF | GRCh38.p7 | 17:67863117 | TTATTGTCTCACAGT[A/C]CTGGAGGCCAGAAGT | 2186 |
| rs62084245 | snp | C/T | 0.401215 | 0.199083 | intron-variant | BPTF | GRCh38.p7 | 17:67871013 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 2186 |
| rs62084246 | snp | C/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67871795 | CTGCTGAACATTTTG[C/G]GTCTCTTTTTCTTTT | 2186 |
| rs62084247 | snp | C/T | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67876787 | CTCCAGCCTGGGCGA[C/T]AGAGCAAGACTTCAT | 2186 |
| rs62084248 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67878425 | GTGGATTTTCTAGGT[C/T]ATGGAGCTGGTTTAT | 2186 |
| rs62084249 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67878882 | TGTTAACCTAATCTC[A/G]TGTTCCTGGGGGTAA | 2186 |
| rs62084251 | snp | A/G | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67882620 | TAAGACTACTGAATG[A/G]CATTTACGACTTTTT | 2186 |
| rs62084252 | snp | C/G | 0.492775 | 0.059668 | intron-variant | BPTF | GRCh38.p7 | 17:67883462 | ACATTATTATAAATT[C/G]AAAACTATGTAACGG | 2186 |
| rs62085978 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BPTF | GRCh38.p7 | 17:67895025 | GGCATAAAGCAAAAA[A/G]TAAGAACCATTTTAT | 2186 |
| rs62085984 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67898945 | AAAAAAAAAAAAATT[A/T]CTAAAAGTACCAGGA | 2186 |
| rs62085985 | snp | A/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67901320 | AAAAAAAAAAAAACC[A/C]AGAACCCTAAAAACA | 2186 |
| rs62085986 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BPTF | GRCh38.p7 | 17:67903573 | TAATTATTTCTTATG[A/G]AAAGGATATAGTATT | 2186 |
| rs62085987 | snp | A/C | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67907184 | AGCAAGACACTGTCT[A/C]CAAAAAAAAAAAAAA | 2186 |
| rs62085988 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BPTF | GRCh38.p7 | 17:67910313 | ACGAATAATGCTGCT[A/G]TGAACATTCATGCAG | 2186 |
| rs62085989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67913357 | CAAAATTGGCCAACT[A/T]ATGTACTAAAGTTTT | 2186 |
| rs62085990 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67920783 | AATTATGAATGTCTA[C/T]TTAGAAAATTCATGA | 2186 |
| rs62085991 | snp | A/G | 0.39709 | 0.20215 | intron-variant | BPTF | GRCh38.p7 | 17:67924392 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCTCG | 2186 |
| rs62085992 | snp | A/T | 0.397271 | 0.202018 | intron-variant | BPTF | GRCh38.p7 | 17:67926967 | GATGTCTCTAAGAGT[A/T]GAAAACTAAGCTCTT | 2186 |
| rs62085993 | snp | C/T | 0.432063 | 0.171327 | intron-variant | BPTF | GRCh38.p7 | 17:67927036 | TATTATATTCAGGTA[C/T]ATAGGATAGGTACAA | 2186 |
| rs62085994 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67930971 | AAAAAAAAAAAAAGT[A/T]CAAAGATTAGCTGGG | 2186 |
| rs62085996 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67950077 | AAAAAAAAAAACATT[A/T]CATAACATATCTTAA | 2186 |
| rs62086041 | snp | A/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67969622 | TTGAATATACCTTAG[A/C]TTATTTAACCAAAAT | 2186 |
| rs62086042 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | BPTF | GRCh38.p7 | 17:67971327 | CAAGGGATCCACCTG[C/T]CTTGCCCTCCCAAAG | 2186 |
| rs62086043 | snp | A/G | 0.439363 | 0.163222 | intron-variant | BPTF | GRCh38.p7 | 17:67971887 | ATTGAACCAGCTTCC[A/G]CTAATAGTGTATATC | 2186 |
| rs62086044 | snp | G/T | 0.434543 | 0.168653 | intron-variant | BPTF | GRCh38.p7 | 17:67974721 | CGATGAACACCAGGT[G/T]GAGAAGATGCACGGG | 2186 |
| rs62086045 | snp | A/G | 0.439224 | 0.163383 | intron-variant | BPTF | GRCh38.p7 | 17:67977615 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 2186 |
| rs63028161 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67851920 | GTGAGATTGGGGTCC[C/T]TTTTTTTTTTTAATG | 2186 |
| rs67006216 | in-del | -/AA | 0.465263 | 0.127129 | intron-variant | BPTF | GRCh38.p7 | 17:67877654 | CTCCAGCCTGGGTGA[-/AA]GAGTGAGACTCTCTC | 2186 |
| rs67013040 | in-del | -/GT/TA | | | intron-variant | BPTF | GRCh38.p7 | 17:67880959 | GTGTGTGTGTGTGTG[-/GT/TA]TATATATATATAATA | 2186 |
| rs67286416 | in-del | -/AT | 0 | 0 | intron-variant, utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982009 | TATATATATATATAT[-/AT]TTAAATATTGGCTTT | 2186 |
| rs67389127 | in-del | -/TG | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67949679 | ATATATATGTATGTG[-/TG]TGTGTATATATATAT | 2186 |
| rs67389128 | snp | C/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67949680 | ATATATATATACACA[C/G]ACATACATATATATA | 2186 |
| rs67648508 | in-del | -/CC/CCGG | | | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896467 | TGAGTAACTAGAAAC[-/CC/CCGG]TGTCCCCCCAGTGCA | 2186 |
| rs68104231 | in-del | -/A | 0.261884 | 0.249717 | intron-variant | BPTF | GRCh38.p7 | 17:67901305 | TGATGAAGAATTGTT[-/A]AAAAAAAAAAAACCC | 2186 |
| rs71142104 | in-del | -/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67870026 | AAAAGGTTTTGCTAA[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs71142105 | in-del | -/C | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67881864 | AAAAAAAAAAAAAAA[-/C]AAAAAACAAAAACCC | 2186 |
| rs71142107 | in-del | -/A | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67909290 | AAAACACTGCAGGAT[-/A]AAAAAAAAAAGGGGG | 2186 |
| rs71142112 | in-del | -/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67950072 | ATATGTTATGAAATG[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs71142113 | in-del | -/T | 0.481087 | 0.0953875 | intron-variant | BPTF | GRCh38.p7 | 17:67950838 | GACTACGTTACTGAA[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs71142114 | in-del | -/A | 0.496034 | 0.0443518 | intron-variant | BPTF | GRCh38.p7 | 17:67954175 | CAATAACAACAAAAA[-/A]CACCCCAAAATTAGC | 2186 |
| rs71142116 | in-del | -/A/AA | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67967149 | TCTCATTAAAAAAAG[-/A/AA]AAAAAAAAAGTATGC | 2186 |
| rs71142117 | in-del | -/T | 0.253824 | 0.249971 | intron-variant | BPTF | GRCh38.p7 | 17:67968786 | TCTAAATTTTCTTTC[-/T]TTTTTTTTTTTTGAG | 2186 |
| rs71142118 | in-del | -/A | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67973508 | TCAAAAAACAAAAAC[-/A]AAAAAAGGGTTTGGG | 2186 |
| rs71142120 | in-del | -/AAAAAAAAAAAAAAAA | 0 | 0 | downstream-variant-500B | BPTF | GRCh38.p7 | 17:67984645 | GTGAAACTCCATCTC[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 2186 |
| rs71354088 | in-del | -/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67827930 | ACTTAATTTTAGTAC[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs71354089 | in-del | -/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67881884 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTGC | 2186 |
| rs71354090 | in-del | -/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67883314 | AGCGAGACTCCATCT[-/T]AAAATAATAATAATA | 2186 |
| rs71354091 | in-del | -/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67905137 | CAGGCAGCCAGGCGC[-/C]GGTGGTTCACGCCTG | 2186 |
| rs71354092 | in-del | -/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67917437 | TGATATTGTCCTTTT[-/T]CTAATATTTTACTAT | 2186 |
| rs71354093 | in-del | -/A | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67952054 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 2186 |
| rs71378916 | snp | A/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67858682 | CAGTTAGCAGGTCAC[A/G]TTCACGCAGTCTCAA | 2186 |
| rs71382152 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67843901 | CTCCCGAGTAGCTGA[A/G]ATTACAGGCATGTGC | 2186 |
| rs71382153 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67844100 | TTTTTTTTTTTTTAA[A/G]ATGGAGTCTCACTCT | 2186 |
| rs71382154 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67844102 | TTTTTTTTTTTAAGA[A/T]GGAGTCTCACTCTGT | 2186 |
| rs71382155 | snp | A/C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67844166 | CTCACTGCAACCTCC[A/C/G]CCTCCCAGGTTCAAG | 2186 |
| rs71382156 | snp | A/G/T | 5.41306e-05 | 0.00520215 | intron-variant | BPTF | GRCh38.p7 | 17:67875511 | ATTTGCCCTGAAGCA[A/G/T]TTTTAAAGAATATCT | 2186 |
| rs71908598 | in-del | -/TTA | | | intron-variant | BPTF | GRCh38.p7 | 17:67853596 | TATTATTATTATTAT[-/TTA]TATTTCCTTAGAGAT | 2186 |
| rs71993218 | in-del | -/CA | | | intron-variant | BPTF | GRCh38.p7 | 17:67880970 | ATATACACACACACA[-/CA]CACACACACGTATAT | 2186 |
| rs72039478 | in-del | -/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67925993 | AACCTAACATATTAC[-/T]TTTTTTTTTTTTTTT | 2186 |
| rs72845272 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | BPTF | GRCh38.p7 | 17:67829033 | GAAGTTTTGATAACT[C/T]TACAGTGGGTGTCAT | 2186 |
| rs72845277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67862439 | GATATGTACCGTCAC[C/T]CTATTTTTCAGATGG | 2186 |
| rs72845278 | snp | C/T | 0.495252 | 0.0484902 | intron-variant | BPTF | GRCh38.p7 | 17:67880960 | TATTATATATATATA[C/T]ACACACACACACACA | 2186 |
| rs72845279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67882969 | CGCCACGCCACTGCA[C/T]TCCAGCCTGGGTGAT | 2186 |
| rs72845280 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | BPTF | GRCh38.p7 | 17:67884568 | CTAGAGGCATGCACT[A/C]CTATGCCTGGCTAAT | 2186 |
| rs72845284 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67917587 | CGTTTGGAAAGGTCT[A/T]ACTAGATTTGTAAGA | 2186 |
| rs72845285 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | BPTF | GRCh38.p7 | 17:67931457 | TCCATCTTGGGCAAC[A/G]GAGTGAGACCCTGTC | 2186 |
| rs72845286 | snp | A/T | 0.0360663 | 0.129354 | intron-variant | BPTF | GRCh38.p7 | 17:67934061 | GAAAAAAGAAAAAAA[A/T]AATAATAATTCATAG | 2186 |
| rs73336738 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67888661 | TTGATCTCACAATCC[A/G]TGAGCCACATTATGA | 2186 |
| rs73336749 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | BPTF | GRCh38.p7 | 17:67894744 | TTGACTAGAAAGAGC[A/T]CTCACATTTTTTAGT | 2186 |
| rs73336764 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | BPTF | GRCh38.p7 | 17:67899169 | AAAATTGCTGAAGCA[A/G]TAATGCAGGTAGACA | 2186 |
| rs73336768 | snp | A/C | 0.030665 | 0.119967 | intron-variant | BPTF | GRCh38.p7 | 17:67901680 | ATTACTTCTCTCATA[A/C]TTAAAAACAATGGGA | 2186 |
| rs73336772 | snp | C/T | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67908056 | GCATTTATCCATTTC[C/T]AATAGGGTTCTGTGA | 2186 |
| rs73338705 | snp | A/G | 0.0144325 | 0.0837134 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67928408 | TTCCACTACTTCCCC[A/G]ACAAGCAGTACAACC | 2186 |
| rs73338706 | snp | C/T | 0.496842 | 0.0396107 | intron-variant | BPTF | GRCh38.p7 | 17:67930488 | ACAGGCCTGAGCCAC[C/T]GCACCTGGCCCAGAT | 2186 |
| rs73338717 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | BPTF | GRCh38.p7 | 17:67935045 | AACACCTACTCTAGG[C/T]AGTTGAAATAAATCA | 2186 |
| rs73338725 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | BPTF | GRCh38.p7 | 17:67941565 | TGCAGAACATGAACC[C/T]CATGTATGTGGACAC | 2186 |
| rs73338734 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67970849 | TTATTGTGTGTAGTT[C/T]TTGCTAGTATAAACA | 2186 |
| rs73338736 | snp | A/C | 0.046775 | 0.145601 | intron-variant | BPTF | GRCh38.p7 | 17:67973562 | AAGCAGTGGTGAGTG[A/C]AGTGGTGCGATCTTG | 2186 |
| rs73350829 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | BPTF | GRCh38.p7 | 17:67836607 | TTATGAACTTATTCA[C/T]AGAGCCTCAAAATAC | 2186 |
| rs73350836 | snp | A/C | 0.030278 | 0.119257 | intron-variant | BPTF | GRCh38.p7 | 17:67838953 | ATTTAGCCACCTATT[A/C]TTTTTTCTAATTGTT | 2186 |
| rs73350838 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67840453 | ATTGGGTTGCTGCTG[C/T]TCCTCTTGTTGTTGT | 2186 |
| rs73350861 | snp | A/G | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67847122 | TAAACATCTTTGAAA[A/G]GAAGTAATAATGGTA | 2186 |
| rs73350867 | snp | A/G | 0.030278 | 0.119257 | intron-variant | BPTF | GRCh38.p7 | 17:67852750 | GGATAAGTTCCAGGA[A/G]GTGGAATTACAGGGT | 2186 |
| rs73350869 | snp | A/G | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67855590 | GTTCCTGAGGGTTTC[A/G]AGAAGCTCTTCTGGG | 2186 |
| rs73350883 | snp | A/G | 0.153332 | 0.230554 | intron-variant | BPTF | GRCh38.p7 | 17:67863312 | ATTTTTTTGAGACAC[A/G]GAGTCTCTGTTGCCC | 2186 |
| rs73350885 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | BPTF | GRCh38.p7 | 17:67864210 | TATAAACTGTATATA[A/G]GCCAAGTAACTAAGT | 2186 |
| rs73350886 | snp | C/T | 0.152667 | 0.230274 | intron-variant | BPTF | GRCh38.p7 | 17:67864387 | CAAAAATTAGCTGGG[C/T]GTGGTGGTGTGTGCC | 2186 |
| rs73350889 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | BPTF | GRCh38.p7 | 17:67867893 | CCAACCCCTCAAACC[C/T]CCAATACTGTACTTT | 2186 |
| rs73350892 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | BPTF | GRCh38.p7 | 17:67872728 | AAGAAAGAAAGAAAA[A/G]AGGAAATCTGTGCCT | 2186 |
| rs73350894 | snp | A/G | 0.030665 | 0.119967 | intron-variant | BPTF | GRCh38.p7 | 17:67873138 | CCAAAAATCCAAGAG[A/G]AGTACTGTGGATATA | 2186 |
| rs73350897 | snp | C/T | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67873882 | ATTCTCCAATTTGTT[C/T]TTCAAAAAAGAACAA | 2186 |
| rs73351760 | snp | C/G | 0.0227819 | 0.104269 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67826204 | CCAGGATTCTGAGGA[C/G]GACGAGGAGGATGAG | 2186 |
| rs73351778 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | BPTF | GRCh38.p7 | 17:67831629 | AGACCCTGTGTCTTC[C/T]CTTTGACTAAAGACC | 2186 |
| rs73351779 | snp | A/G | 0.192715 | 0.243348 | intron-variant | BPTF | GRCh38.p7 | 17:67832639 | TTGACAGAGTTGTGC[A/G]ACCATTAACACTACC | 2186 |
| rs73351787 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | BPTF | GRCh38.p7 | 17:67835159 | AGGCCCTAGTCAGCT[A/G]TGGACCATGCCACCA | 2186 |
| rs73352808 | snp | A/G | 0.479663 | 0.0987666 | intron-variant | BPTF | GRCh38.p7 | 17:67879041 | CAGTCTTTAGTATCA[A/G]GAATATTTTGTCAGT | 2186 |
| rs73352810 | snp | A/G | 0.481703 | 0.0938806 | intron-variant | BPTF | GRCh38.p7 | 17:67879068 | CAGTCTTTAGTATCA[A/G]GAATATTTTGGCCTC | 2186 |
| rs73352815 | snp | G/T | 0.0322045 | 0.12274 | intron-variant | BPTF | GRCh38.p7 | 17:67880616 | ACATTTGTAGGTTTT[G/T]GTTTTTGGTTTTTGG | 2186 |
| rs73352817 | snp | A/G/T | 0.030278 | 0.119257 | intron-variant | BPTF | GRCh38.p7 | 17:67880732 | GCCTGGAACTCCTGA[A/G/T]CTCAAGTGATTATCC | 2186 |
| rs73352835 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67884940 | AGTAGTTTCTTCATA[C/T]AGTTTTATTTTACAT | 2186 |
| rs73994721 | snp | A/T | 0.191147 | 0.242974 | intron-variant | BPTF | GRCh38.p7 | 17:67839334 | TTCCTAAGTTTTTTT[A/T]TAAAAAAAAATCAGC | 2186 |
| rs73994724 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67851552 | AGAATAGAAAATGTT[A/G]GTAGGAGAGAAGATA | 2186 |
| rs73995042 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67866117 | CAGAGTGAGACCCTG[G/T]CTCTAAAATAAATTT | 2186 |
| rs73995044 | snp | A/G | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67867012 | TATCTAACTATATCT[A/G]AACATTTAAAAAGGT | 2186 |
| rs73995045 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67869118 | CAGCTTACTTCCCCC[C/T]TTAATTTCCTTTTAT | 2186 |
| rs73995046 | snp | C/T | 0.067446 | 0.170804 | intron-variant | BPTF | GRCh38.p7 | 17:67870228 | GTGAGATCTGGACCC[C/T]AAAAATGACATAAAT | 2186 |
| rs73995049 | snp | C/T | 0.0681886 | 0.171594 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67887561 | CTATAACTTTGTTTT[C/T]AACCTATCTGAAGTA | 2186 |
| rs73995050 | snp | A/G | 0.0569829 | 0.158885 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67887867 | GCACCAGCAATTTGT[A/G]TTTATATGTTTCCAA | 2186 |
| rs73995052 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67888862 | TGGGGTTGGGTTGCT[A/G]GGGACTTCTATAGGA | 2186 |
| rs73995058 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | BPTF | GRCh38.p7 | 17:67902275 | GTGCTCCATTCCTGG[C/T]CTCTCTCAGTGAAAA | 2186 |
| rs73995064 | snp | C/G | 0.00296871 | 0.0384128 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67911296 | CCTGAGGACTTGATT[C/G]AGGGATGTTCAGAAA | 2186 |
| rs73996923 | snp | A/C/G | 0.00683901 | 0.058076 | missense, synonymous-codon | BPTF | GRCh38.p7 | 17:67940464 | GCAAGTGATGACTCA[A/C/G]ATCATCAGGGGGCAG | 2186 |
| rs73996924 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | BPTF | GRCh38.p7 | 17:67941606 | ACAAAGGTGACATTG[C/T]AGATCATTGAGGAAG | 2186 |
| rs74276828 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67896470 | GTAACTAGAAACTGT[-/TC]CCCCCCAGTGCACAT | 2186 |
| rs74276829 | in-del | -/GG | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67913356 | CAAAATTGGCCAACT[-/GG]AATGTACTAAAGTTT | 2186 |
| rs74348590 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BPTF | GRCh38.p7 | 17:67885853 | TATCCAAAAAATTGT[C/T]TGCCTTGTACTGGAG | 2186 |
| rs74362196 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | BPTF | GRCh38.p7 | 17:67863271 | CAGTTGCTGCCTCTA[C/T]GCTACCTTCTTTTCT | 2186 |
| rs74406086 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67920236 | TTCTTCTCTGTTCAC[C/G]TTTTAAAAAAGACAT | 2186 |
| rs74440135 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | BPTF | GRCh38.p7 | 17:67970933 | GAAAACAGTCTCCAG[A/G]TGAAAGGGTCTAAGT | 2186 |
| rs74444061 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67916951 | AGTTACACAAAGATA[C/T]ATAGTGAATTCCATT | 2186 |
| rs74490420 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | BPTF | GRCh38.p7 | 17:67868281 | TCTCCAGAGGCAATC[A/G]TTATTGCTGTATGTT | 2186 |
| rs74541577 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67857535 | GCAGTGACACTATGT[C/T]GGCTAACTGCAGCCT | 2186 |
| rs74561219 | snp | A/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67857643 | GGCTAATTTTTGCAT[A/T]TTTTGTAGAGACAGG | 2186 |
| rs74599620 | in-del | -/GTGT | | | intron-variant | BPTF | GRCh38.p7 | 17:67878700 | TGTGTGTGTGTGTGT[-/GTGT]CAGTCGTTTAGATAT | 2186 |
| rs74626349 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67978631 | AGTTCAGAAAACAAG[A/T]GGTTCAGGAAAGCAA | 2186 |
| rs74648650 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | BPTF | GRCh38.p7 | 17:67918987 | ACCAGCCTGGCCAAC[A/G]TAGTGAAACCCTGTC | 2186 |
| rs74685511 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67922529 | AGGCTTGGAATAGTG[C/T]TCCAGGTGGAAGAAA | 2186 |
| rs74714051 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | BPTF | GRCh38.p7 | 17:67871722 | GTTGATAGAATATGC[A/G]TATTTAGTATAGATC | 2186 |
| rs74729763 | snp | A/C/G | 0.0267878 | 0.112589 | intron-variant | BPTF | GRCh38.p7 | 17:67975092 | CCGGAGATTCCAACC[A/C/G]TGTTAGGAGCTAAGT | 2186 |
| rs74789884 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | BPTF | GRCh38.p7 | 17:67920486 | GTACCGAGTCTGATA[C/T]GTAAGTGGGTCAATA | 2186 |
| rs74842951 | snp | A/G | 0.0683724 | 0.171789 | intron-variant | BPTF | GRCh38.p7 | 17:67853913 | GTAATGTATTGATTT[A/G]TAATGATGTCACGTC | 2186 |
| rs74859994 | snp | C/T | | | downstream-variant-500B | BPTF | GRCh38.p7 | 17:67984424 | GGTTGGTTAATATGT[C/T]TTCTATAGCTGTTAG | 2186 |
| rs74900812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67861003 | ATTCCTTCTGTCCAC[A/G]TTCAGTTCTGTATGT | 2186 |
| rs74902591 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67836340 | AGGTGCAGTTTATAT[A/G]TTTTACTAGAAATAT | 2186 |
| rs74908807 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | BPTF | GRCh38.p7 | 17:67865938 | AGCATTTACACCATT[G/T]TGTTAGAAATATTTC | 2186 |
| rs74911063 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | BPTF | GRCh38.p7 | 17:67856463 | TGTTTTGGTTTTTCT[A/C]TTTCATATTCAGATG | 2186 |
| rs74935979 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | BPTF | GRCh38.p7 | 17:67936680 | TGCAGTGCTCATTTA[A/T]TGTACTTAAATGAAA | 2186 |
| rs74959789 | snp | C/T | | | missense | BPTF | GRCh38.p7 | 17:67945867 | TCTCTTCAGATACCT[C/T]CCCAAGGCCAGCCAC | 2186 |
| rs74996400 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BPTF | GRCh38.p7 | 17:67876011 | TTTTATATTTTATCA[C/G]CAGACCATAGTGGCA | 2186 |
| rs75015132 | snp | A/G | 0.00666307 | 0.0573336 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67903864 | GAAACAGGAAGAAGA[A/G]GAAACGATGCAGCAA | 2186 |
| rs75033095 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67930969 | CAAAAAAAAAAAAAA[G/T]TTCAAAGATTAGCTG | 2186 |
| rs75033374 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67884434 | CCCTTTTTTTTTTTT[C/T]TGACAAGTTCTCACT | 2186 |
| rs75035861 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67859128 | AGGTACTATATTTTT[A/T]AATTATTATTTTATT | 2186 |
| rs75039453 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | BPTF | GRCh38.p7 | 17:67943967 | ACTCTGGATTGTTGA[C/T]GTTTTTCCTACTAAG | 2186 |
| rs75206973 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | BPTF | GRCh38.p7 | 17:67983650 | TTACACGTTGTATCA[C/G]TGCATTGTGGTAATA | 2186 |
| rs75231441 | snp | A/G | 0.417359 | 0.185718 | intron-variant, utr-variant-5-prime | BPTF | GRCh38.p7 | 17:67889369 | GGCTCTGAATTAGGA[A/G]GCTTTTTAAAAGCAC | 2186 |
| rs75232420 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67835223 | CTCTTAAAAAAAAAA[A/T]TTAAGTAAAATGAAA | 2186 |
| rs75254472 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67942324 | AAAAAAAAGAAAAAC[A/C]AAAAAAAAAGGACAA | 2186 |
| rs75310921 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67859934 | CAGATGACTTTTTAA[A/G]TACCTGTGGGTGATT | 2186 |
| rs75352663 | in-del | -/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67863944 | TTGCTCTTAATTATA[-/T]TTTTAGCAAACCTTT | 2186 |
| rs75360723 | in-del | -/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67886426 | TTTTTTAGTTTTTAA[-/T]TTTTTTAAATGAAAG | 2186 |
| rs75409098 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | BPTF | GRCh38.p7 | 17:67860211 | CTTTAAACATAGTGA[A/T]ATGTGTCAACAATTT | 2186 |
| rs75411880 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67877636 | GGTAAAGTTTTTTTT[G/T]GAGAGAGAGTCTCAC | 2186 |
| rs75442212 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67888592 | GAGACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA | 2186 |
| rs75482863 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | BPTF | GRCh38.p7 | 17:67922388 | TCAAATCCCCCTTCT[C/T]TGTGCGGTGATAGGG | 2186 |
| rs75590500 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | BPTF | GRCh38.p7 | 17:67952661 | CCTATTAATGTTAGC[A/G]TGGCACATTTGTTAG | 2186 |
| rs75603292 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67913565 | TATTTTTATTAGGTA[A/G]TTCATAAAAAATAAG | 2186 |
| rs75615032 | snp | A/G | 0.078151 | 0.181571 | intron-variant | BPTF | GRCh38.p7 | 17:67965579 | CGGTGGTGCACACCT[A/G]TAATCCCAGCTACTA | 2186 |
| rs75652518 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | BPTF | GRCh38.p7 | 17:67903064 | AGGAGTTGTGGCCGA[A/T]GCCTGTGTCTCATGA | 2186 |
| rs75682079 | snp | A/C | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67847676 | CCAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 2186 |
| rs75698710 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | BPTF | GRCh38.p7 | 17:67852119 | TTAATGTCGTTCTCT[A/C]TTTAAACACTGTAGT | 2186 |
| rs75778174 | snp | A/C | | | intron-variant | BPTF | GRCh38.p7 | 17:67877960 | TTGAAATATAACCTG[A/C]AGTAAAGTTTATAAA | 2186 |
| rs75809893 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | BPTF | GRCh38.p7 | 17:67846850 | GGATTACAGGCACAC[A/G]TCACCACACCCAGCT | 2186 |
| rs75812459 | snp | G/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67926338 | TTTTTTTTTTTTTTT[G/T]TTTTGAGATGGAGTC | 2186 |
| rs75816001 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BPTF | GRCh38.p7 | 17:67960040 | CTTACCATTGACGCT[A/T]GTAAAGTAAAATTTG | 2186 |
| rs75819254 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | BPTF | GRCh38.p7 | 17:67846080 | ATAGGGTAACATTCA[C/T]TAGTGGTTGATGAAC | 2186 |
| rs75840459 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67978768 | AAGAAAATGACTCAT[A/G]CATTAGATAATTTGT | 2186 |
| rs75868702 | snp | G/T | | | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67888564 | CACTGCACTCCAGTC[G/T]GGGTGACAGAACGAG | 2186 |
| rs75873575 | in-del | -/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67835626 | AGGGTGAAGAGGAAG[-/T]TAACATGTGATTAGA | 2186 |
| rs75901064 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | BPTF | GRCh38.p7 | 17:67859661 | TCTGCAACTTGCATC[A/G]TTTTAGCTGTTAAAA | 2186 |
| rs75934802 | snp | A/G/T | 6.88895e-05 | 0.00586856 | intron-variant, missense | BPTF | GRCh38.p7 | 17:67946306 | AAGCTTCTAATCAAA[A/G/T]TGAAATCATTCAGAA | 2186 |
| rs75982255 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67884140 | GGGCATTTTCTTTCT[C/T]TTTTTTTTTTTTTTT | 2186 |
| rs76060471 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67909280 | AGGTCCCCCCCCCCC[C/T]TTTTTTTTTTATCCT | 2186 |
| rs76079335 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BPTF | GRCh38.p7 | 17:67936648 | ATGATGAACTACCCA[A/G]CCCTGCCGCCTGGCT | 2186 |
| rs76133941 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67835387 | TAGTCAGTCTGCCTC[A/T]GTTAGACCAGGGGGA | 2186 |
| rs76194753 | in-del | -/AA | | | intron-variant | BPTF | GRCh38.p7 | 17:67933274 | AAGGAAAAAAAAAAA[-/AA]GGTAAAGATCATGGC | 2186 |
| rs76198866 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | BPTF | GRCh38.p7 | 17:67915764 | AGATGTCCCTCCCTT[G/T]TCCTTTCCTCTCTTA | 2186 |
| rs76206641 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | BPTF | GRCh38.p7 | 17:67977112 | GTTTAAGAAAAAATG[A/G]TTGTCAGCCTAGAAG | 2186 |
| rs76221188 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67938760 | AAAGACTAGTCTGGC[C/T]GCATTTTTTAAAATT | 2186 |
| rs76238471 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67850970 | AATAAACAAATGATA[G/T]AATAAGCAAATTGAT | 2186 |
| rs76304234 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | BPTF | GRCh38.p7 | 17:67970846 | TTTTTATTGTGTGTA[C/G]TTTTTGCTAGTATAA | 2186 |
| rs76364327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BPTF | GRCh38.p7 | 17:67932286 | AAAGAAAACAGTCCG[C/T]ATAGCAAAAGACAGA | 2186 |
| rs76412944 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67859913 | GACCTTTGAAATCAC[A/G]TGACTCAGATGACTT | 2186 |
| rs76439337 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67967831 | CAAAAAAAAAAAAAA[A/G]ATTGGAAATGAAATA | 2186 |
| rs76458000 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67961691 | GTCTGTACAAAAAAT[G/T]GGCCAGGCGTGGTGG | 2186 |
| rs76486415 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67955477 | TTCCTGTGAGTTTTT[G/T]GTTTTTGGCTTTTCA | 2186 |
| rs76588593 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67943998 | CAACATAAATATTCT[C/T]ACTTTAGCTTATCTA | 2186 |
| rs76591825 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67916932 | AAATGTCAACAAAGT[A/T]TTCAGTTACACAAAG | 2186 |
| rs76614664 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67948648 | AAAGGTACAGAGACA[C/G]TGAAGTAACGTTGAA | 2186 |
| rs76623333 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | BPTF | GRCh38.p7 | 17:67853561 | ATGTTTTTTCTCATT[C/T]ATATTCTTGTCAAAT | 2186 |
| rs76624702 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67902619 | TGCAGTTAATAGGCA[C/T]GAGCTGTCAGCCTGG | 2186 |
| rs76630910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67878274 | TCCATTATATAGATA[C/T]GTCATGATTCTTGTT | 2186 |
| rs76643626 | snp | A/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67883017 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAAA | 2186 |
| rs76677302 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67926025 | TTTTTTTTTTTTTGA[G/T]ACAAGGTCTCACTCT | 2186 |
| rs76697088 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67924533 | CTGATAAGTTTCTCC[C/T]TTTTTTCCTGCAGAG | 2186 |
| rs76702461 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67958947 | CAAGAGCGAAACTGC[A/G]TCTCAAAAAATATAT | 2186 |
| rs76763785 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67888589 | AACGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 2186 |
| rs76871039 | snp | A/G | 0.0909377 | 0.192871 | intron-variant | BPTF | GRCh38.p7 | 17:67866737 | AGTCTGAGCTAAACC[A/G]TTGGTATGAAATCAC | 2186 |
| rs76897336 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67933261 | GAGACTCCGTCTGAA[A/G]GAAAAAAAAAAAAAG | 2186 |
| rs76952968 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67934410 | GTAATCCCAGCTACT[G/T]GGGAGGCTGAGGCAG | 2186 |
| rs76955879 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | BPTF | GRCh38.p7 | 17:67902343 | TGTATAGAAGCCAAG[C/T]CCTCAAAATCTCCAT | 2186 |
| rs77007748 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67960926 | ATTAAACAGAAATCA[A/G]TTTAGGCATCTTCAC | 2186 |
| rs77022869 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67937261 | GGGAGATAGAGACCA[A/T]CCTGGCTAACACGGT | 2186 |
| rs77030313 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67882165 | AGCAGAATAAAATGT[C/T]TGAGGCTTATGTTAC | 2186 |
| rs77030885 | snp | A/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67926022 | TTTTTTTTTTTTTTT[A/T]GAGACAAGGTCTCAC | 2186 |
| rs77065018 | snp | A/G | 0.00914312 | 0.0669923 | downstream-variant-500B | BPTF | GRCh38.p7 | 17:67984417 | AATGGTTGGTTGGTT[A/G]ATATGTTTTCTATAG | 2186 |
| rs77069333 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | BPTF | GRCh38.p7 | 17:67890061 | CGGGGCTGGAAATTT[A/G]TAGAAATTTCTAGAC | 2186 |
| rs77103901 | in-del | -/AG | 0.417353 | 0.185722 | intron-variant | BPTF | GRCh38.p7 | 17:67826458 | GCCTCCCCCCCAAAC[-/AG]AGGGGAAATGCGACG | 2186 |
| rs77125325 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67960457 | TTCCCCCATTCCTCA[A/G]GCATAACGTCCAACA | 2186 |
| rs77146223 | snp | A/C/G | 0.000137084 | 0.00827804 | synonymous-codon, missense | BPTF | GRCh38.p7 | 17:67959849 | AAAGCTTTACTGTAT[A/C/G]TGTAAAACGCCTTAT | 2186 |
| rs77162708 | snp | A/C | | | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67912763 | AAATCCACTGTCACA[A/C]CCACCACTACAACAG | 2186 |
| rs77178333 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | BPTF | GRCh38.p7 | 17:67882979 | CTGCACTCCAGCCTG[A/G]GTGATAGAGCCAGAC | 2186 |
| rs77183050 | snp | A/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67950074 | AAAAAAAAAAAAAAC[A/T]TTTCATAACATATCT | 2186 |
| rs77207376 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BPTF | GRCh38.p7 | 17:67859429 | AGGATTACAGGCCTG[A/G]GTCACCATGCCCTGC | 2186 |
| rs77217980 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | BPTF | GRCh38.p7 | 17:67978769 | AGAAAATGACTCATA[C/T]ATTAGATAATTTGTT | 2186 |
| rs77218471 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | BPTF | GRCh38.p7 | 17:67829576 | ATTAGGCTAAGTACC[A/G]GTTTCATTGGTTTTT | 2186 |
| rs77221641 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67942881 | AAAAAATACATGTTA[C/T]AATTTCATTTGTATA | 2186 |
| rs77238074 | snp | G/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67895478 | TTTTTTTTTTTTTTT[G/T]TTTGACACAGGATCT | 2186 |
| rs77286406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BPTF | GRCh38.p7 | 17:67877023 | TAGTTCTCTTCTTGA[A/G]TAGAGTAAAAAACAA | 2186 |
| rs77313965 | snp | A/C | | | intron-variant, missense | BPTF | GRCh38.p7 | 17:67945978 | TCCCGTCCTCAGCTA[A/C]AAATACAGCAGCCAC | 2186 |
| rs77341889 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | BPTF | GRCh38.p7 | 17:67938945 | GTAATTGAGGAAATT[G/T]AGCACTGTGATACAT | 2186 |
| rs77343427 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-3-prime, downstream-variant-500B | BPTF | GRCh38.p7 | 17:67983438 | CCAGGCAAATTACCA[A/G]TTACACACAGCTACT | 2186 |
| rs77367375 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67950657 | ATCCTGATCAAGATG[C/G]TGAAACCCCATCTCT | 2186 |
| rs77463059 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67864530 | GAGACTCCATCACAA[A/C]AAAAAAAAAAAAAAA | 2186 |
| rs77511919 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67949682 | ATATATATACACACA[C/G]ACATACATATATATA | 2186 |
| rs77562954 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67961972 | GAGCAAAGCTCTGTC[A/C]AAAAAAAAAAAGAAA | 2186 |
| rs77570471 | snp | A/C | 0.168135 | 0.236216 | intron-variant | BPTF | GRCh38.p7 | 17:67967403 | CCCTCGGCCTCCCCA[A/C]AGTGCTGGGATTACA | 2186 |
| rs77572429 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67880790 | TATAGGCTAATTATC[C/T]TTTTTTTTTCTAGTT | 2186 |
| rs77612826 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | BPTF | GRCh38.p7 | 17:67917013 | ATTTATTTTGAAATA[C/T]GTTTTTAGTATTTTT | 2186 |
| rs77617229 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67939887 | TCCGTCTCAAAAAAA[A/G]GAAAAGCATTATTTG | 2186 |
| rs77634352 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67838674 | TAGTAGAGACGAGGT[C/T]TCACCAGCCCAGGCT | 2186 |
| rs77661970 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | BPTF | GRCh38.p7 | 17:67885783 | TCTGCAATATCTGGC[A/G]CACTGTAAGTTTTGA | 2186 |
| rs77706698 | snp | A/G | 0.3752 | 0.216391 | intron-variant | BPTF | GRCh38.p7 | 17:67957232 | AGGTTGCTGTGAGCC[A/G]AGATCGCGCCATTGC | 2186 |
| rs77766843 | snp | A/G | 0.153332 | 0.230554 | intron-variant | BPTF | GRCh38.p7 | 17:67916952 | GTTACACAAAGATAT[A/G]TAGTGAATTCCATTT | 2186 |
| rs77793512 | snp | C/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67960856 | TATCTAAATGATAAT[C/G]TGTTTGCAAATGCCA | 2186 |
| rs77815345 | snp | G/T | | | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67929355 | TGTTCAAGTACAGCA[G/T]AAAGTCCTGGGTATC | 2186 |
| rs77847648 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | BPTF | GRCh38.p7 | 17:67938508 | ACCAAAATTAGCATG[A/T]TACCAAAGGAAGCAA | 2186 |
| rs77855123 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67911715 | AATGGACTTTGAAGG[A/G]AAACTGGGATGTGAC | 2186 |
| rs77891366 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67921209 | ATTGAGAATCCGTGT[A/C]AAAAAAAAAAAAAAA | 2186 |
| rs77892410 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67894346 | TCTTTCTTTTTTTTT[G/T]GAGACAGAGTCTTGC | 2186 |
| rs77901578 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BPTF | GRCh38.p7 | 17:67870041 | ATTAGCAAAACCTTT[A/T]GTAGTAATGGGGAAC | 2186 |
| rs77928925 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | BPTF | GRCh38.p7 | 17:67828222 | GGTGTGAGCCACCGC[A/G]CCCAGCCTAGTACGT | 2186 |
| rs78026918 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67909291 | CCCCTTTTTTTTTTT[A/T]TCCTGCAGTGTTTTA | 2186 |
| rs78046203 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | BPTF | GRCh38.p7 | 17:67933754 | TCTGAAATACACATT[C/T]ATTTAAAATATTTGT | 2186 |
| rs78127682 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BPTF | GRCh38.p7 | 17:67859431 | GATTACAGGCCTGGG[C/T]CACCATGCCCTGCCT | 2186 |
| rs78177507 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | BPTF | GRCh38.p7 | 17:67916902 | TCAACCACTAAGTTC[A/G]TTTAAGTAGAGTGAA | 2186 |
| rs78191537 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | BPTF | GRCh38.p7 | 17:67972790 | CACATACTTTATTAA[A/G]ATGAAAATTAGTCAA | 2186 |
| rs78209625 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67858706 | GTCTCAAGTGCCCTC[C/T]TGAAAGGAGCTCATA | 2186 |
| rs78216963 | snp | A/C/G | 0.00874735 | 0.0655527 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67903834 | AGAAAAGGAGAAAGT[A/C/G]AAAAAAAAAGAGAAG | 2186 |
| rs78222435 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67842118 | TATAATTGTACATAT[G/T]TGTATATATCTTTAT | 2186 |
| rs78226081 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67957029 | GGCTCACGCCTGTAA[C/T]CCTAGCACTTTGGGA | 2186 |
| rs78234879 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67861357 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCACT | 2186 |
| rs78273096 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67966291 | TGCCAGCATCACTCA[C/G]TGACGGCTCATCATG | 2186 |
| rs78345390 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67835219 | CCATCTCTTAAAAAA[A/G]AAATTTAAGTAAAAT | 2186 |
| rs78357051 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | BPTF | GRCh38.p7 | 17:67936674 | TGGCTGTGCAGTGCT[C/T]ATTTAATGTACTTAA | 2186 |
| rs78428480 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67859130 | GTACTATATTTTTTA[A/T]TTATTATTTTATTTT | 2186 |
| rs78452260 | snp | G/T | 0.401215 | 0.199083 | intron-variant | BPTF | GRCh38.p7 | 17:67852406 | CAAGTACTATAAAAA[G/T]ATTCTTATATGACCT | 2186 |
| rs78527639 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BPTF | GRCh38.p7 | 17:67970707 | TCTTAAATAGAAATA[A/G]GTTTAAATGAATTAT | 2186 |
| rs78584448 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | BPTF | GRCh38.p7 | 17:67851763 | ATACCAGTTTACAGT[C/G]CCAGTGGTGGTATAC | 2186 |
| rs78593993 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67952409 | TCTGGGATTACAGAC[A/G]CCTGCTACCACGCCC | 2186 |
| rs78597152 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67978770 | GAAAATGACTCATAC[A/G]TTAGATAATTTGTTT | 2186 |
| rs78628269 | in-del | -/TTT | | | intron-variant | BPTF | GRCh38.p7 | 17:67909460 | TGTCTTTTTTTTTTT[-/TTT]AAATGAAAAAATGAA | 2186 |
| rs78814593 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67864561 | GGAAAAGAAAAAAGT[A/T]AAACAAAACAAAACA | 2186 |
| rs78833304 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | BPTF | GRCh38.p7 | 17:67942931 | ACTAAGCTATTTTGT[A/G]TAGGGATACAGGGCT | 2186 |
| rs78841307 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | BPTF | GRCh38.p7 | 17:67965360 | AAAAAAAAGAAAAAC[A/G]GGATCGAGATGGTTT | 2186 |
| rs78856267 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67961689 | CCGTCTGTACAAAAA[A/T]TTGGCCAGGCGTGGT | 2186 |
| rs78933019 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | BPTF | GRCh38.p7 | 17:67879974 | GGCAGGACAAACATC[C/T]AAACTATCCAAACTA | 2186 |
| rs79045504 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67899549 | TTTTTTTTTTTTTTT[G/T]GAGACAGAATCTTGT | 2186 |
| rs79045622 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67927904 | ATTTTTTTTTTTTTA[G/T]AGATGGAGTCACTCT | 2186 |
| rs79076582 | snp | A/C/G/T | 0.0050638 | 0.0500632 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67911798 | ATAGCAGTGAAGAAG[A/C/G/T]TATGATTGTTCAGAA | 2186 |
| rs79091930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67850861 | GCTCTGCATTGTTCT[A/G]TGTGGGAAACATGCT | 2186 |
| rs79102238 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | BPTF | GRCh38.p7 | 17:67848796 | CTAATTAGAATACCT[A/G]TACATTGTAACATAA | 2186 |
| rs79110709 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | BPTF | GRCh38.p7 | 17:67892166 | ATTTTCTCTGTTTCC[A/G]AAACTGTAGTAGTTA | 2186 |
| rs79143204 | snp | A/G | 0.021333 | 0.101051 | intron-variant | BPTF | GRCh38.p7 | 17:67878738 | TTTTGGGAGGTACCT[A/G]TCTGCTTCTTTGTTC | 2186 |
| rs79182912 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | BPTF | GRCh38.p7 | 17:67976073 | ACCTTAAATATCTTT[A/T]AAAAAAAAATAAATA | 2186 |
| rs79192674 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | BPTF | GRCh38.p7 | 17:67973951 | TCTGCATGCTGCCAC[A/G]CTTTTCATTACCACA | 2186 |
| rs79199220 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67934409 | TGTAATCCCAGCTAC[A/T]TGGGAGGCTGAGGCA | 2186 |
| rs79201731 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67951208 | CTCTCTCTCTCTCTC[C/T]TTTTCTCAGAGGTTG | 2186 |
| rs79204002 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67899550 | TTTTTTTTTTTTTTT[G/T]AGACAGAATCTTGTT | 2186 |
| rs79293437 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67876823 | AAAAGTAAAAAAAGA[A/G]AAAAAGAAAATATAT | 2186 |
| rs79334122 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67840122 | TTTTTTTTTTTTTTT[G/T]AGATAGGGTCTTGCT | 2186 |
| rs79460712 | snp | A/C | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67968787 | AGCGAGACACGTCTC[A/C]AAAAAAAAAAAGAAA | 2186 |
| rs79501063 | snp | C/T | 0.154993 | 0.231244 | intron-variant | BPTF | GRCh38.p7 | 17:67977938 | CGGCTCACCACAAGC[C/T]CCACCTCCCGGATTC | 2186 |
| rs79511468 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67868130 | ATAATTCAATGTCAC[C/T]TTATTTATTTTGTTA | 2186 |
| rs79551791 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67849311 | GCTTTTCAAACTTCA[C/G]TGACCATATAAATCA | 2186 |
| rs79555068 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67838494 | ACATACTTTTTTTTT[G/T]GAGCTGGAGTATCGC | 2186 |
| rs79573603 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67923074 | TTTTTTTTTTTTTTT[G/T]AGACAGGATCTTGCT | 2186 |
| rs79583830 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | BPTF | GRCh38.p7 | 17:67913889 | CAGTAATTTGCCTGT[C/G]GCTACAGAGACACAG | 2186 |
| rs79602862 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | BPTF | GRCh38.p7 | 17:67851846 | TAAATTTTTTTCCAT[C/T]GAGGAGTCTGAGAAC | 2186 |
| rs79627915 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67967817 | GAGCGAGACTCTGTC[A/C]AAAAAAAAAAAAAGA | 2186 |
| rs79658927 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | BPTF | GRCh38.p7 | 17:67828166 | CGAACTCTTGACCTC[C/G]TGATCCGCCTACCTC | 2186 |
| rs79688954 | snp | A/G | 0.128288 | 0.218372 | intron-variant | BPTF | GRCh38.p7 | 17:67921232 | AAAAAAAAAAAAAAA[A/G]AAAGAAATACAGGCC | 2186 |
| rs79717019 | in-del | -/C | 0.423719 | 0.179783 | intron-variant | BPTF | GRCh38.p7 | 17:67826581 | TCGCTCGCTCTCTCT[-/C]CCCCCCCCAACCCCC | 2186 |
| rs79726130 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67886957 | GAACATCCTTAACGT[A/G]TATCTTTGTGTACTT | 2186 |
| rs79757812 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BPTF | GRCh38.p7 | 17:67900873 | AATTGGCCAGGCATG[A/G]TCTTGCTTGCCTGTA | 2186 |
| rs79764686 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67960852 | GTGCTATCTAAATGA[A/T]AATCTGTTTGCAAAT | 2186 |
| rs79835257 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67851918 | TAGTGAGATTGGGGT[C/T]CTTTTTTTTTTTTAA | 2186 |
| rs79888593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67947886 | AGTTCTGAGTTTATA[C/G]TTGTTTATCTTGATT | 2186 |
| rs79902495 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | BPTF | GRCh38.p7 | 17:67866309 | CATTTCTCAGAGTAA[A/G]TCAAGTTTGAGTGAG | 2186 |
| rs79912512 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67926934 | TTTTCTTTCTTTTTT[A/T]AACTGATTTAATCAG | 2186 |
| rs79918595 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67897894 | AATTATGGCCCTGTC[G/T]TCTTTATTAATATTT | 2186 |
| rs79971042 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67954401 | GCAAGCTTATTTTGA[C/G]TGAGAGGAGTTTTGT | 2186 |
| rs79971226 | snp | A/G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67944926 | GGGGACAGCCAAGAA[A/G/T]CAGGGCCCAGGCTTC | 2186 |
| rs79993364 | in-del | -/CT | 0.494526 | 0.0520291 | intron-variant | BPTF | GRCh38.p7 | 17:67852461 | TATCCCCTTGCCCTC[-/CT]CTTTTTATTTTTAGT | 2186 |
| rs80016183 | in-del | -/ATT | | | intron-variant | BPTF | GRCh38.p7 | 17:67907256 | GTTTTGGGAGGCTTG[-/ATT]TTTTTTTTTTTTTTG | 2186 |
| rs80043429 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BPTF | GRCh38.p7 | 17:67859493 | ATAAAGAGACTAAAT[A/C]TCAAAGAGGTTAAAT | 2186 |
| rs80135947 | snp | A/C | 0.417359 | 0.185718 | intron-variant | BPTF | GRCh38.p7 | 17:67839885 | GCTGTACCATTTTGC[A/C]TTCTTACCTGCAAGT | 2186 |
| rs80168212 | in-del | -/TT | | | intron-variant | BPTF | GRCh38.p7 | 17:67851930 | GGTCCTTTTTTTTTT[-/TT]AATGCAGGAAAATTA | 2186 |
| rs80200826 | snp | G/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67857174 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 2186 |
| rs80201495 | snp | C/T | 0.0127342 | 0.0787713 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | BPTF | GRCh38.p7 | 17:67918795 | TTTGAGATGGGATGA[C/T]ATGGCGGCCAAGGCT | 2186 |
| rs80224301 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67976714 | AAAAAAAAAAAAAAA[A/G]ATAAGAATAAAAGAA | 2186 |
| rs80278110 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67967816 | AGAGCGAGACTCTGT[A/C]AAAAAAAAAAAAAAG | 2186 |
| rs80289706 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67937273 | CCAGCCTGGCCAACA[A/T]GGTGAAATCCCCATC | 2186 |
| rs80291777 | snp | A/G | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67933264 | ACTCCGTCTGAAGGA[A/G]AAAAAAAAAAAGGTA | 2186 |
| rs80332262 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | BPTF | GRCh38.p7 | 17:67952602 | TTTTACGTGCAGAAC[A/G]TACAGTTCCCATATT | 2186 |
| rs80345645 | snp | A/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67909289 | CCCCCCTTTTTTTTT[A/T]TATCCTGCAGTGTTT | 2186 |
| rs111328898 | snp | A/G | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67909009 | CCAGATAATTTTTGT[A/G]TTTTTAGTAGAGATC | 2186 |
| rs111335433 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67953029 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAAGCT | 2186 |
| rs111344045 | snp | C/T | 0.5 | 0 | synonymous-codon | BPTF | GRCh38.p7 | 17:67944269 | GCAGCTAATGCAAGC[C/T]GCAATGCCAAATGGT | 2186 |
| rs111351421 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | BPTF | GRCh38.p7 | 17:67838532 | CCCAAGCTGGAGTGC[A/G]GTGGCACAATCTTGG | 2186 |
| rs111364363 | snp | C/T | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67844127 | CTCTGTCACCCAGGC[C/T]GGAGTGCAGTGGCAT | 2186 |
| rs111396695 | snp | A/G | 4.95929e-05 | 0.00497936 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67912901 | ACGGGAGGCACACTG[A/G]TTACATCTATGACTG | 2186 |
| rs111419590 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67864948 | TAGCTGAGACGACAG[A/G]CGCCTGCCACCATGC | 2186 |
| rs111456700 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67982701 | TTGTTGCAAAAAAGA[C/T]GCTTTTTTATTGCTG | 2186 |
| rs111470720 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | BPTF | GRCh38.p7 | 17:67967550 | CATTGGAAATGGCGG[A/G]GTGGCTCACGCTGGA | 2186 |
| rs111500034 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67887665 | TTAAACTAGCTTAAG[A/T]GAAGAGGGAATTTAA | 2186 |
| rs111509620 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67922189 | AATCACTTCTCTTTG[A/G]CTTGTATCCCTTTGT | 2186 |
| rs111515047 | in-del | -/T/TT | 0.215747 | 0.247642 | intron-variant | BPTF | GRCh38.p7 | 17:67967140 | TTTAATTGTGCATAC[-/T/TT]CTTTTTTTTTCTTTT | 2186 |
| rs111534384 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | BPTF | GRCh38.p7 | 17:67865236 | GATTAAGGGAACTCC[A/C]CCCATATCCTTTTAT | 2186 |
| rs111572403 | snp | C/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67949652 | GTACATATATATATA[C/T]ACACACAGACATATA | 2186 |
| rs111586446 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | BPTF | GRCh38.p7 | 17:67895522 | GCTGGAGTACAGTGG[C/T]GCCATCACAGCTCAC | 2186 |
| rs111597099 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BPTF | GRCh38.p7 | 17:67870360 | AAGAGAAGGGGACAC[A/G]GACATTTTTGGGTGC | 2186 |
| rs111689906 | snp | C/T | 0.030665 | 0.119967 | intron-variant | BPTF | GRCh38.p7 | 17:67858834 | CTTACCCTTTGGATA[C/T]TCACTCTCACTGCCT | 2186 |
| rs111733114 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67960919 | GTGCTGAATTAAACA[C/G]AAATCAATTTAGGCA | 2186 |
| rs111766505 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67823889 | TCTCGGCTCACTGCA[A/G]CCTCCACCTCCCAGG | 2186 |
| rs111785673 | snp | A/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67904972 | CTGCAGAATTACTAG[A/T]TTAGTTTACTAAAAC | 2186 |
| rs111837975 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67947919 | AGTTCATTAAATGAG[A/G]ACACTTGGCACTAAT | 2186 |
| rs111857534 | snp | C/T | 0.192401 | 0.243274 | intron-variant | BPTF | GRCh38.p7 | 17:67908857 | TTTTTTTTGTTGACA[C/T]GGAGTCTCACTCTGT | 2186 |
| rs111867548 | snp | C/T | 0.157311 | 0.232183 | intron-variant, upstream-variant-2KB | BPTF | GRCh38.p7 | 17:67897122 | ACCTGAGGTCGGGAA[C/T]TCGAGACCAGCCTGA | 2186 |
| rs111904805 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | BPTF | GRCh38.p7 | 17:67971764 | AGCCAAGATCGTTGC[A/G]TTGCAGTGATCTGAG | 2186 |
| rs111924567 | snp | A/G | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67841132 | AGATAGTAAGGCCAG[A/G]CATGGTGGCTCATGC | 2186 |
| rs111973081 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67826460 | CTCCCCCCCAAACAG[A/G]GGGGAAATGCGACGG | 2186 |
| rs111978423 | snp | A/G | 0.0383715 | 0.133092 | utr-variant-3-prime | BPTF | GRCh38.p7 | 17:67983684 | TCTATAAAATCTGCC[A/G]TAGTTGGATTATGCA | 2186 |
| rs111987481 | snp | A/C/G | 1.64727e-05 | 0.00286986 | missense | BPTF | GRCh38.p7 | 17:67944228 | TTGATACCTCAAGGG[A/C/G]TGACTGTACTCCCAG | 2186 |
| rs112064971 | snp | G/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67955979 | ATGGCAAAACCCTGT[G/T]TCTACAAAAAAGAAT | 2186 |
| rs112082977 | in-del | -/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67835661 | CTGCCACAGTCCTGG[-/T]AATTTTTTTTTTTTT | 2186 |
| rs112100881 | snp | A/G/T | 1.66543e-05 | 0.00288563 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67912655 | ACAGAAGTCACCACG[A/G/T]TGACCTCCACAGTGG | 2186 |
| rs112125458 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | BPTF | GRCh38.p7 | 17:67908199 | AGTCTTGCTCTGTCA[G/T]CCAGGCTGGAGTGCA | 2186 |
| rs112134422 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67883609 | TTGTTTTGTTTGTGT[A/G]TGTTTTTTGAGACAG | 2186 |
| rs112196399 | snp | A/C/G | 0 | 0 | splice-donor-variant, intron-variant | BPTF | GRCh38.p7 | 17:67924590 | GAGCAACAGGCTAAG[A/C/G]TTAGTGAACAGAAGA | 2186 |
| rs112222385 | snp | C/T | 0.417196 | 0.185864 | intron-variant | BPTF | GRCh38.p7 | 17:67844408 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 2186 |
| rs112224314 | snp | A/G | 0.000567064 | 0.0168289 | missense | BPTF | GRCh38.p7 | 17:67948253 | GAGCAGCTCAGAGCC[A/G]AGATCCTGAAGAAGA | 2186 |
| rs112256045 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67960957 | TTTTCATTATCTTAT[C/G]TCATTGGAAATTATA | 2186 |
| rs112256587 | snp | C/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67879807 | TTCTAACAGTCAGCT[C/T]TAGTGGGAACTAATA | 2186 |
| rs112258244 | snp | C/T | 4.95307e-05 | 0.00497623 | synonymous-codon, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67913008 | AGCTCTGCCATCCTA[C/T]AGAAAATTTGTTACC | 2186 |
| rs112280949 | snp | C/G | 0.156319 | 0.231784 | intron-variant | BPTF | GRCh38.p7 | 17:67844066 | CACCGTGCCCGGCCC[C/G]CGCCTTTTTTTTTTT | 2186 |
| rs112307543 | snp | A/G | 0.177182 | 0.23916 | intron-variant | BPTF | GRCh38.p7 | 17:67896112 | GGACTATAGGCACCC[A/G]CCACTATGCCCAGCT | 2186 |
| rs112315617 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67915135 | ATGATCTTTGTTATT[A/G]ATGTTAAGGCTGAGC | 2186 |
| rs112351030 | in-del | -/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67853595 | TCACAAATGCAGTTA[-/T]TTATTATTATTATTA | 2186 |
| rs112352201 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67832677 | AGCACGTTTTTATAC[C/T]CCCGCAAAAGAAGCC | 2186 |
| rs112365809 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | BPTF | GRCh38.p7 | 17:67953183 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT | 2186 |
| rs112390700 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | BPTF | GRCh38.p7 | 17:67859606 | TATTTTCAATACCTT[A/G]TTTTATACTGTAGTC | 2186 |
| rs112399193 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | BPTF | GRCh38.p7 | 17:67961676 | ACATAGAGAGACCCC[A/G]TCTGTACAAAAAATT | 2186 |
| rs112421831 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BPTF | GRCh38.p7 | 17:67949676 | ACATATATATATATA[C/T]ACACAGACATACATA | 2186 |
| rs112425819 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | BPTF | GRCh38.p7 | 17:67835421 | TACCTAACATCTCTT[A/T]TTCTCTAGCCTTTTA | 2186 |
| rs112464681 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BPTF | GRCh38.p7 | 17:67840633 | CTTGGCTCACTGGAG[C/T]CCGTCATTCCCCGCC | 2186 |
| rs112474554 | snp | A/G | | | intron-variant | BPTF | GRCh38.p7 | 17:67893241 | CTTTTAGACTTCAAA[A/G]GTTCTATCATAAGAT | 2186 |
| rs112487679 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BPTF | GRCh38.p7 | 17:67873317 | ACAAAAATTAGCCGG[G/T]TGTGGTGGCAGGCGC | 2186 |
| rs112606425 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67952614 | AACGTACAGTTCCCA[C/T]ATTATTCCTCCCCCA | 2186 |
| rs112636457 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67978621 | TGTTTATTTGAGTTC[A/G]GAAAACAAGTGGTTC | 2186 |
| rs112641140 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67911603 | AACCGCTCATACAGG[A/G]GGAAAGTGACACCAT | 2186 |
| rs112651248 | in-del | -/AG | 0.494315 | 0.0530107 | intron-variant | BPTF | GRCh38.p7 | 17:67876820 | TAAAAAAGTAAAAAA[-/AG]AGAAAAAGAAAATAT | 2186 |
| rs112660275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67955764 | TCCTGAAGGCAGAGA[C/T]TGCAGTGAGCCGAGA | 2186 |
| rs112664844 | snp | A/C | 0.040671 | 0.13668 | intron-variant | BPTF | GRCh38.p7 | 17:67928129 | CCTCAGGTGATCCAC[A/C]CACCTCAGCCTCCCA | 2186 |
| rs112680343 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67859311 | CCACCGTGCCCAGCT[A/G]ATTTTTTTATTTTTT | 2186 |
| rs112719119 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | BPTF | GRCh38.p7 | 17:67909074 | TCCTGACCTCAGGTG[A/C]TGCACCCACCTCGGC | 2186 |
| rs112734041 | snp | A/T | 0 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67975267 | GTGGACACTTATCAA[A/T]CCAGTCATGAATGGT | 2186 |
| rs112774543 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BPTF | GRCh38.p7 | 17:67857449 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGACAGCAG | 2186 |
| rs112777887 | snp | C/G | 0.5 | 0 | missense | BPTF | GRCh38.p7 | 17:67945505 | CAAGTGTGGGTCCAG[C/G]AGAAGCCCAGCCACA | 2186 |
| rs112810626 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67967325 | TTTTATATTTTTTGT[A/T]GAGACAGGGTTTCAC | 2186 |
| rs112821420 | snp | A/G/T | 3.61749e-05 | 0.00425278 | intron-variant | BPTF | GRCh38.p7 | 17:67964427 | CCCTCTGTGTGCAGC[A/G/T]TTTCAAAATGAAATC | 2186 |
| rs112823619 | snp | A/C | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67906318 | TCTCTTGACTTTGTG[A/C]TCTGCCCGCCTCGGC | 2186 |
| rs112826391 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | BPTF | GRCh38.p7 | 17:67934467 | GGGGTTGCAGTGAGC[A/G]GAGATTGCACCACTG | 2186 |
| rs112831201 | in-del | -/A | 0.192715 | 0.243348 | intron-variant, downstream-variant-500B | BPTF | GRCh38.p7 | 17:67929964 | CTACAAAAAATACAG[-/A]AATTAGCCAGGCGTG | 2186 |
| rs112842409 | snp | A/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67828615 | CTCACTGCAACCTCC[A/T]CCTCCTGGGTTCAAG | 2186 |
| rs112854398 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | BPTF | GRCh38.p7 | 17:67870930 | GCCCGCCACTACGCC[C/T]GGCTAATTTTTTGTA | 2186 |
| rs112882142 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BPTF | GRCh38.p7 | 17:67966079 | GGGGGAAATAAAAGG[A/G]TATAGTGCACTGGAT | 2186 |
| rs112884549 | snp | C/T | 0.000457771 | 0.015122 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67826074 | CCCGGACCACCGCGG[C/T]CCGGAGGGCCGTCAA | 2186 |
| rs112885816 | snp | G/T | 0.375 | 0.216506 | intron-variant | BPTF | GRCh38.p7 | 17:67881858 | GGATTTTGGGTTTTT[G/T]TTTTTTTTTTTTTTT | 2186 |
| rs112921129 | snp | A/G | 0.00321917 | 0.0399903 | missense, nc-transcript-variant | BPTF | GRCh38.p7 | 17:67911387 | AAGATCGAGTGTTAG[A/G]TGATGTCTCCATTCG | 2186 |
| rs112926011 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | BPTF | GRCh38.p7 | 17:67840125 | TTTTTTTTTTTTGAG[A/T]TAGGGTCTTGCTTGT | 2186 |
| rs112927623 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67961922 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 2186 |
| rs112935935 | snp | C/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67906952 | GATGGGATGCCAAGG[C/G]AGGGGAGGATCAGTT | 2186 |
| rs112963276 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BPTF | GRCh38.p7 | 17:67859228 | ATGGCTCACTGCAGC[A/C/G]TCAGTCTCCTAGGCT | 2186 |
| rs113004842 | snp | A/G | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67961875 | GCTACTCGGGAGGCC[A/G]AGTCAGGAGAATCGC | 2186 |
| rs113010619 | snp | G/T | | | intron-variant | BPTF | GRCh38.p7 | 17:67954392 | TTAAGTTTTGCAAGC[G/T]TATTTTGAGTGAGAG | 2186 |
| rs113013698 | snp | C/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67976034 | TGTCTAACGATTCAA[C/T]CAGTGCAGTTTATGG | 2186 |
| rs113039026 | in-del | -/T | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67832964 | GGCTAATTTTTTGTA[-/T]TTTTTTTTTTTTTTA | 2186 |
| rs113053140 | in-del | -/TGGA | 0.5 | 0 | intron-variant | BPTF | GRCh38.p7 | 17:67873992 | AAAGTAAGAAAATGC[-/TGGA]TGGATGGATGGATGG | 2186 |