SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1246 | snp | C/T | 0.11228 | 0.208646 | intron-variant | TAF3 | GRCh38.p7 | 10:7859920 | ATATTTAGGATGAGA[C/T]GGATTGAGAGGCATG | 83860 |
rs155415 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | TAF3 | GRCh38.p7 | 10:7936996 | gccataaaaagatac[A/G]gaggaatctgaaatg | 83860 |
rs166411 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:8010210 | CAATGAAGAAATGCA[C/T]CTTggctgggcatgg | 83860 |
rs174498 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | TAF3 | GRCh38.p7 | 10:7969830 | GAGCTGGAATTTCCA[C/G]CCCGGTCAGTGTGGC | 83860 |
rs187821 | snp | A/G | 0.365439 | 0.221752 | intron-variant | TAF3 | GRCh38.p7 | 10:7939559 | TTTCTTCTATTTCCT[A/G]CATTGTCTCTATTTC | 83860 |
rs192346 | snp | A/G | 0.232943 | 0.249417 | intron-variant | TAF3 | GRCh38.p7 | 10:7932793 | ctactctaggggctg[A/G]ggtgggaggactgct | 83860 |
rs196527 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7994652 | TAATGTGAAAGAAAA[G/T]ATGTggctgggcgca | 83860 |
rs196528 | snp | A/G | 0.460589 | 0.13473 | intron-variant | TAF3 | GRCh38.p7 | 10:7983431 | CAGGGCAAAGAACCT[A/G]GTTGGTGTACAAAAG | 83860 |
rs197449 | snp | A/G | 0.262985 | 0.249663 | intron-variant | TAF3 | GRCh38.p7 | 10:7912061 | TATCTCCCAAACTAC[A/G]ATGACATAAAAGCAA | 83860 |
rs263414 | snp | C/T | 0.420733 | 0.18262 | intron-variant | TAF3 | GRCh38.p7 | 10:7944017 | TGGTTTTGCATTCTT[C/T]CTCTTACGCATATCA | 83860 |
rs263415 | snp | C/T | 0.420733 | 0.18262 | intron-variant | TAF3 | GRCh38.p7 | 10:7943276 | AAGCAGAACGTGATG[C/T]GTAGGAGCCAGAATC | 83860 |
rs263416 | snp | A/T | 0.180064 | 0.240019 | intron-variant | TAF3 | GRCh38.p7 | 10:7931367 | CAGGGTCAGCAGGAA[A/T]ATAAATATGGCATAG | 83860 |
rs263417 | snp | G/T | 0.420255 | 0.183066 | intron-variant | TAF3 | GRCh38.p7 | 10:7930347 | AACCTATTCATGGAT[G/T]ATTAAGAATTTGTTA | 83860 |
rs263430 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7987631 | TTCTAAAAGGCTATA[C/T]CAATTAAAATTCTCA | 83860 |
rs263431 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7987477 | AGTCACCAGTTTTCA[A/T]ACATTTAAGTTGTCA | 83860 |
rs263432 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7986880 | GCAAAACACTTAAAA[A/G]TCTGATCAGGACATA | 83860 |
rs265933 | snp | C/T | 0.418007 | 0.185132 | intron-variant | TAF3 | GRCh38.p7 | 10:7912944 | CCACAGACTGGGTGG[C/T]TTAAGCAACAGCAGT | 83860 |
rs265934 | snp | A/G | 0.417196 | 0.185864 | intron-variant | TAF3 | GRCh38.p7 | 10:7913757 | acttgtgcctcttta[A/G]ggatacagtaagagg | 83860 |
rs265935 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | TAF3 | GRCh38.p7 | 10:7914371 | GCAGGTGttttcccc[C/G]tcctatttcaatcat | 83860 |
rs265937 | snp | A/C | 0.352287 | 0.228117 | intron-variant | TAF3 | GRCh38.p7 | 10:7915865 | GCACCTGTAATCCAG[A/C]TACTTGGGAGGCTGA | 83860 |
rs265940 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7958892 | ccacctcagcctccc[A/C]aagtgctggggatta | 83860 |
rs377957 | snp | C/T | 0.428182 | 0.17536 | intron-variant | TAF3 | GRCh38.p7 | 10:7956212 | GTGAGACACCGCGCC[C/T]GGCCTATTTTTTAAT | 83860 |
rs389606 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7979980 | AATTTGAATGTTACA[A/T]ATTTTCATGTGTCAT | 83860 |
rs406846 | snp | A/G | 0.179425 | 0.239831 | intron-variant | TAF3 | GRCh38.p7 | 10:7909917 | TCAGGGACCTGAGCA[A/G]TCGTGGAGCTGGGTA | 83860 |
rs407644 | snp | C/T | 0.160938 | 0.233598 | intron-variant | TAF3 | GRCh38.p7 | 10:7966448 | AACTGATAGAAACCC[C/T]GCAGTTTTGTAGGCA | 83860 |
rs415641 | snp | A/G | 0.180064 | 0.240019 | intron-variant | TAF3 | GRCh38.p7 | 10:7955209 | TGCCCCACCTCTCCC[A/G]TGCTGTCTAAGCATT | 83860 |
rs449682 | snp | A/G | 0.231189 | 0.249291 | intron-variant | TAF3 | GRCh38.p7 | 10:7963322 | ATAGAGAAAGATGGC[A/G]TTTACTGGTTAGGAA | 83860 |
rs458116 | snp | C/T | 0.428333 | 0.175206 | intron-variant | TAF3 | GRCh38.p7 | 10:7956061 | ATAATTACCTAATTA[C/T]AGTATAATTTTGGGA | 83860 |
rs464199 | snp | A/G | 0.00484259 | 0.0489678 | intron-variant | TAF3 | GRCh38.p7 | 10:7924689 | TTTCAATTTTTCTGT[A/G]ATGCTACACATATTT | 83860 |
rs466858 | snp | G/T | 0.254105 | 0.249966 | intron-variant | TAF3 | GRCh38.p7 | 10:7923590 | GTTTTGTTTTGTTTT[G/T]TTTTTTTGCTATACA | 83860 |
rs474334 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953796 | CTCTGTGTTAACTAG[A/G/T]ACTAATTCATTCATT | 83860 |
rs474388 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7953780 | ACTAATTCATTCATT[C/T]GCCTATGATGTGCAC | 83860 |
rs474467 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7953750 | CTCTGAATCTCACTA[G/T]GGAAAGTTCTGTGTT | 83860 |
rs476901 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008081 | aaaaGATTGTTCCCA[C/G]ACGGGCTGCAGAGGT | 83860 |
rs497482 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975064 | caacagaacaagact[C/T]tgtctcaaaaaaaaa | 83860 |
rs500915 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8007842 | TTTATTataaaaagc[A/G]ctatttattgaggac | 83860 |
rs500948 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8007828 | cactatttattgagg[A/G]cctataagaagttag | 83860 |
rs501874 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007722 | cttttgtagatgagg[A/G]aactgaagatcagca | 83860 |
rs502031 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007660 | CTTTTGAACCAAAGT[C/G]TACTTGATTCCAAAG | 83860 |
rs531053 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007804 | AAGTTAGAGGTTATA[C/T]TAGGCACTTTACAAA | 83860 |
rs768165 | snp | A/T | 0.0707826 | 0.174302 | intron-variant | TAF3 | GRCh38.p7 | 10:8005671 | TGATGGAACCAAAGC[A/T]AAAGGGAAAAGCAGG | 83860 |
rs768166 | snp | A/C | 0.364401 | 0.222289 | intron-variant | TAF3 | GRCh38.p7 | 10:8005587 | TTAGGCAAGTCTGAT[A/C]TTTGGTTATGATGAA | 83860 |
rs768167 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:8005311 | TCTTTAAAAAAAATA[A/C]GCAGCACATAATCAA | 83860 |
rs794551 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830689 | gggtttcaccatgtt[A/G]gccaggctggtctgg | 83860 |
rs794552 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830696 | accatgttggccagg[A/C]tggtctggaactcct | 83860 |
rs794553 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830744 | cagcctcggcctccc[A/C]aagtgctgggattcc | 83860 |
rs794555 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915519 | agtagctgggactac[A/G]ggcgcctgccaccac | 83860 |
rs794556 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | TAF3 | GRCh38.p7 | 10:7915373 | acaggcgtgagccac[C/T]gcgcccggccCATGA | 83860 |
rs797015 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830650 | caccacgcccagcta[A/C]tttttgtatttttag | 83860 |
rs811195 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7915367 | atgagccaccgcgcc[C/T]ggccCAAAAGTGATC | 83860 |
rs877345 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:8011813 | ATCTACTGGAAAACC[A/C]GAACTTTTAGAGCTA | 83860 |
rs914607 | snp | A/T | 0.178465 | 0.239547 | intron-variant | TAF3 | GRCh38.p7 | 10:7934459 | agactctgtctcaaa[A/T]aaataaataaataaa | 83860 |
rs914608 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7934216 | ATTTTCTTAATAGAT[C/T]GCTCATCCATACATT | 83860 |
rs951096 | snp | A/G | 0.441021 | 0.161279 | intron-variant | TAF3 | GRCh38.p7 | 10:7930647 | TACCTGAGTACAGTC[A/G]TCAATATTTTTAAGC | 83860 |
rs975101 | snp | A/G | 0.347253 | 0.230308 | intron-variant | TAF3 | GRCh38.p7 | 10:7878671 | TGAATTAATTATAGT[A/G]CATCTAGAGAGGGAA | 83860 |
rs1018699 | snp | C/T | 0.184203 | 0.241186 | intron-variant | TAF3 | GRCh38.p7 | 10:7882044 | CAACTCTGCTCAGTT[C/T]AGTTTTGAACTCACT | 83860 |
rs1018700 | snp | A/G | 0.480144 | 0.097642 | intron-variant | TAF3 | GRCh38.p7 | 10:7880109 | tgagattacaggtgc[A/G]tgccaccaaggccag | 83860 |
rs1018701 | snp | C/T | 0.332106 | 0.236133 | intron-variant | TAF3 | GRCh38.p7 | 10:7878227 | GCATTTGCTATTTTA[C/T]ATTACTTTCTTTAAA | 83860 |
rs1041541 | snp | A/C | 0.36021 | 0.224397 | intron-variant | TAF3 | GRCh38.p7 | 10:7880306 | AATGAAGGCACTCTG[A/C]TAAATCAAAGTTATT | 83860 |
rs1057735 | snp | A/G | 1.66081e-05 | 0.00288163 | missense | TAF3 | GRCh38.p7 | 10:7964891 | GGAACCTCAAGTTCC[A/G]ATAACTCATGGACAA | 83860 |
rs1064134 | snp | A/G | 0.482905 | 0.0908579 | intron-variant | TAF3 | GRCh38.p7 | 10:7856796 | tatctaaaggactcc[A/G]aagccaacttaAAGA | 83860 |
rs1244229 | snp | C/T | 0.399722 | 0.200208 | missense | TAF3 | GRCh38.p7 | 10:7965597 | AGGAGAAAGAGAAGG[C/T]GAAGGAGAAAGAAAA | 83860 |
rs1244440 | snp | A/G | 0.431621 | 0.171796 | intron-variant | TAF3 | GRCh38.p7 | 10:7890600 | TTAAATTCTAATCAG[A/G]CAATCAACACTCACA | 83860 |
rs1244441 | snp | A/G | 0.429388 | 0.174127 | intron-variant | TAF3 | GRCh38.p7 | 10:7890401 | CTACTATGATGGAAC[A/G]TAGACTACAAACACA | 83860 |
rs1244455 | snp | G/T | 0.13446 | 0.221699 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817005 | agttgaagtgtacac[G/T]tgagtctatgatttt | 83860 |
rs1244456 | snp | C/T | 0.4628 | 0.13121 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817144 | ACAGATTTGtgaaat[C/T]caaggcgcaagagag | 83860 |
rs1244457 | snp | C/T | 0.299664 | 0.245017 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817171 | AGAGTTTCAATGTTA[C/T]Agaagcgttcaacat | 83860 |
rs1244458 | snp | A/C | 0.183568 | 0.241012 | intron-variant | TAF3 | GRCh38.p7 | 10:7887784 | AAAGGATTTTAATAA[A/C]CCAAAAGGTATAACC | 83860 |
rs1244459 | snp | A/G | 0.231189 | 0.249291 | intron-variant | TAF3 | GRCh38.p7 | 10:7886277 | TGGTAAACATTAGGG[A/G]GCGGCTGGTTATGTC | 83860 |
rs1244460 | snp | A/C | 0.184838 | 0.241358 | intron-variant | TAF3 | GRCh38.p7 | 10:7881848 | CTTTTCTTTTTAATG[A/C]GTTAACTAGGGCACA | 83860 |
rs1244461 | snp | C/T | 0.421368 | 0.182025 | intron-variant | TAF3 | GRCh38.p7 | 10:7881545 | TACGTTCCAGCTTCA[C/T]TGCTAAATTTTATAC | 83860 |
rs1244462 | snp | A/G | 0.455144 | 0.142885 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819059 | AGTCATCCTTCGGGT[A/G]CCTCTTCCTTATCCG | 83860 |
rs1244463 | snp | A/G | 0.089084 | 0.191327 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819580 | GCTACAGTACTTATG[A/G]GTTTTAAATGAATGT | 83860 |
rs1244464 | snp | C/T | 0.427423 | 0.176128 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820036 | CTAGCATTTTGCTTA[C/T]CTTTTGCCAGCCTGC | 83860 |
rs1244465 | snp | C/T | 0.464735 | 0.128019 | intron-variant | TAF3 | GRCh38.p7 | 10:7822944 | ATTACATTTGAAAAT[C/T]TATAGATAAATTATC | 83860 |
rs1244466 | snp | C/T | 0.381697 | 0.212499 | intron-variant | TAF3 | GRCh38.p7 | 10:7823012 | cagctactcagaagg[C/T]gaaggtaggaggatg | 83860 |
rs1244467 | snp | A/G | 0.464841 | 0.127841 | intron-variant | TAF3 | GRCh38.p7 | 10:7823120 | cctgtctcaaaaaac[A/G]aacaaaaaCCAAACT | 83860 |
rs1244468 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | TAF3 | GRCh38.p7 | 10:7823733 | tccgcctcctgggtt[C/T]gagcagttctcctgc | 83860 |
rs1244469 | snp | C/T | 0.300421 | 0.244863 | intron-variant | TAF3 | GRCh38.p7 | 10:7823922 | aggcgtgagccatcg[C/T]gcccagctAAGATGC | 83860 |
rs1244470 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | TAF3 | GRCh38.p7 | 10:7824244 | CATATTTACTTACta[C/T]tttttcttaatattt | 83860 |
rs1244471 | snp | C/T | 0.489588 | 0.0713983 | intron-variant | TAF3 | GRCh38.p7 | 10:7824594 | TTCATATGTTAGTGA[C/T]TATTTTAATGGATTT | 83860 |
rs1244472 | snp | A/T | 0.464735 | 0.128019 | intron-variant | TAF3 | GRCh38.p7 | 10:7824613 | TTTAATGGATTTTTA[A/T]TCCTCTTAGCTTTCC | 83860 |
rs1244473 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | TAF3 | GRCh38.p7 | 10:7825188 | ATATTTAAGTAATTT[C/G]TGGTCTCTAACACAA | 83860 |
rs1244474 | snp | A/G | 0.464735 | 0.128019 | intron-variant | TAF3 | GRCh38.p7 | 10:7825414 | atacattgttattca[A/G]ccatcatccccatcc | 83860 |
rs1244475 | snp | G/T | 0.468249 | 0.121932 | intron-variant | TAF3 | GRCh38.p7 | 10:7825583 | ttataaatggacttg[G/T]acattatttgtcttt | 83860 |
rs1244476 | snp | A/C | 0.316726 | 0.240931 | intron-variant | TAF3 | GRCh38.p7 | 10:7827785 | actctgtctcaaaaa[A/C]aaaaaaaaaaacaaa | 83860 |
rs1244477 | snp | A/C | 0.474091 | 0.11083 | intron-variant | TAF3 | GRCh38.p7 | 10:7827791 | tctcaaaaaaaaaaa[A/C]aaaaacaaaaacaaa | 83860 |
rs1244478 | snp | A/G | 0.433818 | 0.169443 | intron-variant | TAF3 | GRCh38.p7 | 10:7827851 | gtagtcccagctatc[A/G]gagtctgtggtggga | 83860 |
rs1244479 | snp | A/G | 0.498774 | 0.02473 | intron-variant | TAF3 | GRCh38.p7 | 10:7828181 | gaggctgtagtgcgc[A/G]atgattgagcctgtg | 83860 |
rs1244480 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | TAF3 | GRCh38.p7 | 10:7828361 | AGCTGTGTGATTATC[C/T]GCAGTGTGAAGATGA | 83860 |
rs1244481 | snp | C/G | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7849663 | aaaGTTCGCATGAAC[C/G]CCCCCAATAGTTGTT | 83860 |
rs1244482 | snp | A/C | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7849544 | CCACAACTATTATGC[A/C]CATTTAAAACACAAT | 83860 |
rs1244483 | snp | A/C | 0.0991586 | 0.199366 | intron-variant | TAF3 | GRCh38.p7 | 10:7849487 | CATACAATGCTTATG[A/C]AACATAAATTCACAC | 83860 |
rs1244484 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | TAF3 | GRCh38.p7 | 10:7849327 | TCACTTGTAGTAATA[G/T]AATCTAAAGACAAAA | 83860 |
rs1244485 | snp | C/T | 0.309648 | 0.24278 | intron-variant | TAF3 | GRCh38.p7 | 10:7847904 | tgggtgcctgtagtc[C/T]cagctactcgggagg | 83860 |
rs1244486 | snp | A/C | 0.300673 | 0.244811 | intron-variant | TAF3 | GRCh38.p7 | 10:7846704 | CTCATCATGTCTTAG[A/C]TTTATAGGAGGTCCA | 83860 |
rs1244487 | snp | A/G | 0.300673 | 0.244811 | intron-variant | TAF3 | GRCh38.p7 | 10:7846597 | AGCCTCTAGGAAAGA[A/G]TAAAAATCATGAAAT | 83860 |
rs1244488 | snp | A/G | 0.378568 | 0.214407 | intron-variant | TAF3 | GRCh38.p7 | 10:7846404 | AAAATCACAAATGCA[A/G]ATAAAGCAACTATCA | 83860 |
rs1244489 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7845998 | gcactccagcctggg[C/T]gacaggcgagacatt | 83860 |
rs1244490 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | TAF3 | GRCh38.p7 | 10:7845878 | ATCTGTTGCCTTCAA[C/T]GCATTTGAAAAGAAA | 83860 |
rs1244491 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | TAF3 | GRCh38.p7 | 10:7844930 | TTTGATGCAACATTG[C/T]aatattttaaaatat | 83860 |
rs1244492 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | TAF3 | GRCh38.p7 | 10:7844501 | taatcccaactactc[A/G]ggaggctgaggcagg | 83860 |
rs1244493 | snp | A/G | 0.499683 | 0.0125759 | intron-variant | TAF3 | GRCh38.p7 | 10:7858827 | CATGCAGGCGCGCGC[A/G]CACACACACACACAC | 83860 |
rs1244494 | snp | A/G | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7840912 | cagtgagccgagatc[A/G]cgccattgcacgcca | 83860 |
rs1244495 | snp | A/C | 0.382279 | 0.212137 | intron-variant | TAF3 | GRCh38.p7 | 10:7839376 | CCATAGGTTTTCTGC[A/C]AAAAAAATGGTGAAA | 83860 |
rs1244496 | snp | A/T | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7839099 | GCAACGAGGGGCAAG[A/T]AACTAACATGTCAAG | 83860 |
rs1244497 | snp | C/T | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7838019 | caagattaaatgaga[C/T]aatgtttatgaaTAT | 83860 |
rs1244498 | snp | A/G | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7836569 | ATGTGGAAATGggcc[A/G]ggtgcagtggctcac | 83860 |
rs1244499 | snp | C/G | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7836406 | atgcctctaatccca[C/G]gtactcgggaggctg | 83860 |
rs1244500 | snp | G/T | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7836356 | accagggagccggag[G/T]ttgtgccattgtact | 83860 |
rs1244501 | snp | C/T | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7836347 | ccggaggttgtgcca[C/T]tgtactccagcctgg | 83860 |
rs1244502 | snp | C/T | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7835821 | CAACATGCCACCAAG[C/T]GCCATGAGACCCGAG | 83860 |
rs1244503 | snp | C/G | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7835536 | CTCGCTGAGAGGACA[C/G]AGCTGGCAGTGGAAT | 83860 |
rs1244504 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | TAF3 | GRCh38.p7 | 10:7832750 | ccagcctggccaaca[C/T]ggtgaaatcgcatct | 83860 |
rs1244505 | snp | C/T | 0.464947 | 0.127663 | intron-variant | TAF3 | GRCh38.p7 | 10:7831640 | AAACTGTAATGAGGC[C/T]GGGCACGGTAGCTCA | 83860 |
rs1244506 | snp | C/T | 0.498109 | 0.0306926 | intron-variant | TAF3 | GRCh38.p7 | 10:7831308 | aaatctgtgagttca[C/T]aatgatagagtatta | 83860 |
rs1244507 | snp | C/T | 0.498109 | 0.0306926 | intron-variant | TAF3 | GRCh38.p7 | 10:7830994 | aaaactggacatcat[C/T]agctgatatcttgcc | 83860 |
rs1244508 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830523 | gcactccagcctggg[C/T]gacagagcaagactc | 83860 |
rs1244509 | snp | A/T | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7850361 | AAAGCTATATCATAC[A/T]TAAATTTAAAGTTAA | 83860 |
rs1244510 | snp | C/T | 0.487933 | 0.0767327 | intron-variant | TAF3 | GRCh38.p7 | 10:7852949 | ctagttgtgcatatg[C/T]tttttgaaagtatca | 83860 |
rs1244511 | snp | A/G | 0.465158 | 0.127307 | intron-variant | TAF3 | GRCh38.p7 | 10:7853117 | tggcaaatgttgttt[A/G]atattcagtcagttt | 83860 |
rs1270824 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830631 | ctgggcgtggtggca[G/T]gcacctgtagtccca | 83860 |
rs1270825 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830608 | tagtcccagctactc[A/G]ggaggctgaggcaga | 83860 |
rs1271906 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | TAF3 | GRCh38.p7 | 10:7829761 | cccctcttcccctac[C/T]gtgctctttggaaag | 83860 |
rs1272533 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7841457 | ATAGTACTGGAGCAC[A/T]CTGTTTTCCTTTAAG | 83860 |
rs1312777 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863666 | tatatatatgtgtgt[A/G]tatatatatGTGTGT | 83860 |
rs1312778 | snp | A/T | 0.300926 | 0.244758 | intron-variant | TAF3 | GRCh38.p7 | 10:7863499 | ccttagcctcctgag[A/T]agctgggataacagg | 83860 |
rs1312779 | snp | A/G | 0.392325 | 0.205532 | intron-variant | TAF3 | GRCh38.p7 | 10:7863375 | gacctgcctgcctca[A/G]cctcccaaagtgctg | 83860 |
rs1312780 | snp | A/G | 0.392511 | 0.205404 | intron-variant | TAF3 | GRCh38.p7 | 10:7863180 | tatgaaaatgcaaag[A/G]actcagtgtcaagaa | 83860 |
rs1312781 | snp | G/T | 0.499563 | 0.0147699 | intron-variant | TAF3 | GRCh38.p7 | 10:7862986 | aatgttcatatcaac[G/T]ttatttgaaatagtc | 83860 |
rs1312782 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | TAF3 | GRCh38.p7 | 10:7862395 | TGGAGTTTGAGTTGA[A/G]CTAAGGTAACTTCCT | 83860 |
rs1312783 | snp | A/C | 0.392696 | 0.205275 | intron-variant | TAF3 | GRCh38.p7 | 10:7861916 | cacaagtttaattgg[A/C]gtctcagaaggagat | 83860 |
rs1312784 | snp | C/T | 0.392696 | 0.205275 | intron-variant | TAF3 | GRCh38.p7 | 10:7861269 | aatacaaaaattagc[C/T]gtgcagggccggatg | 83860 |
rs1312785 | snp | C/T | 0.392325 | 0.205532 | intron-variant | TAF3 | GRCh38.p7 | 10:7860587 | aatcaagcatttatc[C/T]tttttgtttttttct | 83860 |
rs1314661 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | TAF3 | GRCh38.p7 | 10:7861628 | atggaggttatgaga[C/T]ggtggaaaaatatct | 83860 |
rs1399181 | snp | C/T | 0.498652 | 0.0259235 | intron-variant | TAF3 | GRCh38.p7 | 10:7927325 | ATGTTCAGAAAAACA[C/T]GTAGAAAAAGGTCAA | 83860 |
rs1399182 | snp | C/T | 0.496245 | 0.0431677 | intron-variant | TAF3 | GRCh38.p7 | 10:7927051 | CACCTAGTTATCCCA[C/T]TGTCATGATCTTATC | 83860 |
rs1399183 | snp | C/T | 0.49621 | 0.0433651 | intron-variant | TAF3 | GRCh38.p7 | 10:7927023 | ATCGTTTTCTGTGTT[C/T]ATCCCCCACCCCATG | 83860 |
rs1514233 | snp | A/T | 0.421209 | 0.182174 | intron-variant | TAF3 | GRCh38.p7 | 10:7924326 | AAAATCAAAACATGC[A/T]AGCAGAGAACCACCG | 83860 |
rs1556479 | snp | A/G | 0.43309 | 0.17023 | intron-variant | TAF3 | GRCh38.p7 | 10:7864496 | tagcaatgtgactac[A/G]gttaagaataatata | 83860 |
rs1625706 | snp | C/T | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7842115 | CAATGACAAACAGGG[C/T]CATCTTTAATTAAAT | 83860 |
rs1630998 | snp | A/G | 0.382473 | 0.212016 | intron-variant | TAF3 | GRCh38.p7 | 10:7842957 | CCGGAGGATATTATT[A/G]CAAATGCATATATTT | 83860 |
rs1758643 | snp | A/G | 0.299158 | 0.245119 | intron-variant | TAF3 | GRCh38.p7 | 10:7862886 | atggaacaatactca[A/G]caataaaaaggagta | 83860 |
rs1758645 | snp | C/T | 0.300673 | 0.244811 | intron-variant | TAF3 | GRCh38.p7 | 10:7855158 | tcttaggtttccgca[C/T]tgctggcttgggatt | 83860 |
rs1758652 | snp | A/T | 0.499801 | 0.00998203 | intron-variant | TAF3 | GRCh38.p7 | 10:7843518 | AACATCTTCAATATG[A/T]CTAAGGGTTCAAAAA | 83860 |
rs1758653 | snp | A/G | 0.298651 | 0.24522 | intron-variant | TAF3 | GRCh38.p7 | 10:7843020 | ACAGACACAGACTAC[A/G]CCCTAGCAGGTGCAA | 83860 |
rs1758654 | snp | A/G | 0.299158 | 0.245119 | intron-variant | TAF3 | GRCh38.p7 | 10:7842597 | CCATTAGGTATCATC[A/G]GACAAATATATATAT | 83860 |
rs1758655 | snp | A/G | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7842369 | AGTTCAAGACCAGCC[A/G]GGGCAATATACTGAA | 83860 |
rs1782687 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856687 | gatttggaaaaagcc[A/C]tttttctaaggagcc | 83860 |
rs1782688 | snp | C/T | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7854814 | GTTCCAAATGGCTTC[C/T]ATGCTACTGTAACAT | 83860 |
rs1782690 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | TAF3 | GRCh38.p7 | 10:7843379 | GCTCATGCCTGTTAT[C/T]CCACCACTTTAGGAG | 83860 |
rs1887581 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | TAF3 | GRCh38.p7 | 10:8000758 | AGGGTCTCACTCTGC[C/T]GCCCAGGCTAAAGTG | 83860 |
rs1887582 | snp | C/T | 0.331642 | 0.236293 | intron-variant | TAF3 | GRCh38.p7 | 10:7961370 | CAGATGGAGAACGCG[C/T]GAGATGATGCATGGG | 83860 |
rs1887583 | snp | A/G | 0.463774 | 0.129618 | intron-variant | TAF3 | GRCh38.p7 | 10:7961354 | GAGATGATGCATGGG[A/G]AAGTACTTAGTAAAT | 83860 |
rs1983939 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7986569 | TTAGCTCCAAAAGTT[G/T]CCCAAGCTGAACAAA | 83860 |
rs1983940 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986888 | CTTAAAAGTCTGATC[A/G]GGACATAATAGGCTT | 83860 |
rs1989346 | snp | A/G | 0.105924 | 0.204309 | intron-variant | TAF3 | GRCh38.p7 | 10:7863427 | ATCAGCCTGGCCAGG[A/G]TGGTGAAACCCCGTC | 83860 |
rs2025911 | snp | A/C | 0.350982 | 0.228698 | intron-variant | TAF3 | GRCh38.p7 | 10:7923766 | TGGATGATCAACTAT[A/C]GCAATATTTGTATAG | 83860 |
rs2026396 | snp | C/T | 0.350546 | 0.22889 | intron-variant | TAF3 | GRCh38.p7 | 10:7885068 | ctccattccccaccc[C/T]cagcccttccaagta | 83860 |
rs2026397 | snp | A/C | 0.494143 | 0.0537956 | intron-variant | TAF3 | GRCh38.p7 | 10:7922586 | TCACCAGGCAGTCAT[A/C]TCAACATGTCATGCT | 83860 |
rs2057604 | snp | C/T | 0.325563 | 0.238307 | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818302 | CTAAAACACTGGCGT[C/T]TTCGTCACCGCTGTC | 83860 |
rs2065430 | snp | A/T | 0.182296 | 0.240658 | intron-variant | TAF3 | GRCh38.p7 | 10:7900062 | TGGATATCTTTTCAA[A/T]ATATTTTAACAGACA | 83860 |
rs2065431 | snp | G/T | 0.49263 | 0.0602539 | intron-variant | TAF3 | GRCh38.p7 | 10:7916472 | TATTAGCAGATACAC[G/T]GACATATTTTTAGAA | 83860 |
rs2077854 | snp | A/G | 0.030278 | 0.119257 | intron-variant | TAF3 | GRCh38.p7 | 10:7984342 | GTTTTACTGTGCAGT[A/G]AAAGTATTTCTGAAA | 83860 |
rs2137853 | snp | C/G/T | 0.00150523 | 0.0273928 | intron-variant | TAF3 | GRCh38.p7 | 10:8009060 | GTCAACAAAAGAAGA[C/G/T]AAGGTAAAAGTCAAA | 83860 |
rs2137854 | snp | C/G | 0.492823 | 0.0594727 | intron-variant | TAF3 | GRCh38.p7 | 10:7916962 | AGCCTATGTTCTTTC[C/G]AGCACACAACAGACA | 83860 |
rs2149111 | snp | C/T | 0.498459 | 0.0277128 | intron-variant | TAF3 | GRCh38.p7 | 10:7936457 | TGATATGCCAATCCA[C/T]AGAAATCTCTGCTTT | 83860 |
rs2151013 | snp | G/T | 0.438105 | 0.164671 | intron-variant | TAF3 | GRCh38.p7 | 10:7881262 | AAAAGAGCTTGTGGG[G/T]TTTTTTTTTGTTTTT | 83860 |
rs2151014 | snp | C/T | 0.347914 | 0.230028 | intron-variant | TAF3 | GRCh38.p7 | 10:7879010 | CCAGGCGCGGTGACT[C/T]ATGCCTGTAATCCCA | 83860 |
rs2151015 | snp | A/G | 0.446118 | 0.155041 | intron-variant | TAF3 | GRCh38.p7 | 10:7877078 | AAGGACAGTAACAGC[A/G]TAAAAAATAAACCTC | 83860 |
rs2151016 | snp | C/T | 0.445987 | 0.155207 | intron-variant | TAF3 | GRCh38.p7 | 10:7877059 | AAAATAAACCTCAGA[C/T]GTGGAATCTCCATTA | 83860 |
rs2151017 | snp | C/T | 0.362941 | 0.223034 | intron-variant | TAF3 | GRCh38.p7 | 10:7876156 | GAAAAATATAAAACA[C/T]CGCACAAAATTAATT | 83860 |
rs2151018 | snp | A/G | 0.1652 | 0.235179 | intron-variant | TAF3 | GRCh38.p7 | 10:7876009 | AAAGTTTAATAGTAT[A/G]ATAAAAAAACTTAAA | 83860 |
rs2182860 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7916162 | CAAGGTTTCTATCTT[C/T]TAAAGAACCTGAACA | 83860 |
rs2182861 | snp | C/T | 0.494057 | 0.0541878 | intron-variant | TAF3 | GRCh38.p7 | 10:7936068 | TGTTTTACGATACAA[C/T]CACACTAGTCCAGGA | 83860 |
rs2183940 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7869945 | GTAATCTCTGGGCCA[A/G]CCAAAACCCAGGGGT | 83860 |
rs2388429 | snp | A/T | 0.299158 | 0.245119 | intron-variant | TAF3 | GRCh38.p7 | 10:7850018 | AAAATAGGGAATATT[A/T]TTTGTTAAAAATTGT | 83860 |
rs2388430 | snp | A/T | 0.465788 | 0.126237 | intron-variant | TAF3 | GRCh38.p7 | 10:7850686 | tctcaaaaaaaaaaa[A/T]atatatatgtatata | 83860 |
rs2388431 | snp | G/T | 0.488302 | 0.0755777 | intron-variant | TAF3 | GRCh38.p7 | 10:7938968 | AAGCCGTAAGGATAA[G/T]AGAGCAAGGGAAGAG | 83860 |
rs2458639 | snp | A/G | 0.159292 | 0.232964 | intron-variant | TAF3 | GRCh38.p7 | 10:7951587 | caaagcaagtcacac[A/G]gccacccaaaatcat | 83860 |
rs2482628 | snp | G/T | 0.396182 | 0.202807 | intron-variant | TAF3 | GRCh38.p7 | 10:7856680 | aaaaagccatttttc[G/T]aaggagcccttgttc | 83860 |
rs2490303 | snp | C/T | 0.417034 | 0.18601 | intron-variant | TAF3 | GRCh38.p7 | 10:7887969 | TGGAACTTTCCAAGC[C/T]CTTGAATTCATATTT | 83860 |
rs2490304 | snp | C/T | 0.463559 | 0.129972 | intron-variant | TAF3 | GRCh38.p7 | 10:7858042 | TCTACTGAGGCCGTT[C/T]AAACCTCTTTGTAAG | 83860 |
rs2490305 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842164 | AAACAAAAAAAAAAA[A/C]AAAAAAAAAAAACAA | 83860 |
rs2769369 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7994668 | TTTTCTTTCACATTA[A/G]AAATCCTGAGTCTTg | 83860 |
rs2778470 | snp | C/G | 0.46173 | 0.132931 | intron-variant | TAF3 | GRCh38.p7 | 10:7858836 | ATTCAGTGACATGCA[C/G]GCGCGCGCACACACA | 83860 |
rs2778471 | snp | A/G | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7842088 | AAATAGGGTACTCAC[A/G]CAACTCAATGAACGA | 83860 |
rs2778473 | snp | C/G | 0.299916 | 0.244966 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817762 | TCGGCTGCCTACAGA[C/G]GCCAAACCGAGCCTT | 83860 |
rs2778476 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867062 | catgttcaccaggct[A/C]gtctcagactcctga | 83860 |
rs2802457 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | TAF3 | GRCh38.p7 | 10:7844121 | TTAAGTATATTCATA[C/T]GTAACTATTCTCACA | 83860 |
rs2986977 | snp | A/G | 0.413416 | 0.189196 | intron-variant | TAF3 | GRCh38.p7 | 10:7908595 | TAAATCTGGGTTACC[A/G]AGCGCTTCTGAAGGA | 83860 |
rs2986978 | snp | A/G | 0.178465 | 0.239547 | intron-variant | TAF3 | GRCh38.p7 | 10:7953698 | TGTTTGATTAAGGAC[A/G]GCCAATCATGTCTTA | 83860 |
rs2986980 | snp | G/T | 0.408871 | 0.193029 | intron-variant | TAF3 | GRCh38.p7 | 10:7957794 | CGCTCTCTCTAGCGC[G/T]CTCTCTCTCTCTCTC | 83860 |
rs2990215 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | TAF3 | GRCh38.p7 | 10:7914920 | AAAGGCTGGGAGCAC[C/G]GAGGCTTTCAGGGGC | 83860 |
rs3039468 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881502 | acacacacacacaca[-/CA]CTAGATAGCAGGTTT | 83860 |
rs3824659 | snp | C/G | 0.000235349 | 0.0108452 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965049 | GGAGGAAGGCAGCTT[C/G]GTTTTCTCCTCATAC | 83860 |
rs3858258 | snp | A/C | 0.441021 | 0.161279 | intron-variant | TAF3 | GRCh38.p7 | 10:7947086 | TGAAGAGAAAGTATA[A/C]GCAAGTATAAGAAAG | 83860 |
rs3889643 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7947291 | TTAACCGCACTATCC[A/G]GCCTGCGGTGGGGGC | 83860 |
rs3898015 | snp | C/T | 0.441705 | 0.160466 | intron-variant | TAF3 | GRCh38.p7 | 10:7975860 | TTTATGTATTTCAAG[C/T]TCATGAATTACATCA | 83860 |
rs3932551 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914366 | TTGAAGCAGGTGTTT[C/T]CCC | 83860 |
rs4277004 | snp | G/T | 0.498346 | 0.0287064 | intron-variant | TAF3 | GRCh38.p7 | 10:7979153 | ATCGAGACCATCCTG[G/T]CTAACACGGTGAAAC | 83860 |
rs4344398 | snp | C/T | 0.121717 | 0.214577 | intron-variant | TAF3 | GRCh38.p7 | 10:7979160 | ccatcctgtctaaca[C/T]ggtgaaaccccttct | 83860 |
rs4373822 | snp | C/T | 0.375 | 0.216506 | intron-variant | TAF3 | GRCh38.p7 | 10:7863674 | atatatatacacaca[C/T]atatatatatacaca | 83860 |
rs4617489 | snp | A/G | 0.330016 | 0.236849 | intron-variant | TAF3 | GRCh38.p7 | 10:7850630 | GCAGTGAGCTGAGAT[A/G]GTGCCACTGCACTCC | 83860 |
rs4747603 | snp | C/G | 0.499741 | 0.0113788 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817119 | CACCCAGGGTGGCGG[C/G]GGTAGCGGGACAGAT | 83860 |
rs4747622 | snp | C/T | 0.365439 | 0.221752 | intron-variant | TAF3 | GRCh38.p7 | 10:7887648 | AAAACAGATAAGAGC[C/T]GCTGGGAGTGTTTTG | 83860 |
rs4747628 | snp | A/G | 0.498133 | 0.030494 | intron-variant | TAF3 | GRCh38.p7 | 10:7912690 | TAGAGACTTTTGCAG[A/G]TATCAGAGTTAGTAC | 83860 |
rs4747629 | snp | C/T | 0.496105 | 0.0439572 | intron-variant | TAF3 | GRCh38.p7 | 10:7913043 | ACCTCTTTCCTCGGC[C/T]TGCAGGTGGGCGCCT | 83860 |
rs4747631 | snp | A/G | 0.440746 | 0.161604 | intron-variant | TAF3 | GRCh38.p7 | 10:7918254 | GAGAGACGAGAATGT[A/G]TGAAATGGTCTTCAT | 83860 |
rs4747641 | snp | C/T | 0.485799 | 0.0830599 | intron-variant | TAF3 | GRCh38.p7 | 10:7944521 | AATGTAGATTTGCAA[C/T]GTTAAAGGACATAGC | 83860 |
rs4747643 | snp | C/T | 0.498525 | 0.0271165 | intron-variant | TAF3 | GRCh38.p7 | 10:7944906 | TTTTTTTCCAGAATT[C/T]TGTCAAGGTCATTTA | 83860 |
rs4747647 | snp | A/G | 0.478093 | 0.102341 | missense | TAF3 | GRCh38.p7 | 10:7964835 | CCACTTCCGCGAACA[A/G]TTTCACAAAGTCAGG | 83860 |
rs4747649 | snp | A/G | 0.319856 | 0.240042 | intron-variant | TAF3 | GRCh38.p7 | 10:7968535 | TCATCTTTAGAAATA[A/G]TGATAAGAACACTAA | 83860 |
rs4747654 | snp | A/G | 0.441841 | 0.160303 | intron-variant | TAF3 | GRCh38.p7 | 10:7975511 | AAGCTGGAATTAAAA[A/G]TGTTCTTTGGCATCA | 83860 |
rs4749282 | snp | A/G | 0.109108 | 0.206518 | intron-variant | TAF3 | GRCh38.p7 | 10:7825756 | cactgatggacattt[A/G]ggttgtttcaacctt | 83860 |
rs4749283 | snp | C/G | 0.445987 | 0.155207 | intron-variant | TAF3 | GRCh38.p7 | 10:7826058 | TATTTGTCTCAGGAA[C/G]TATGTTTAAATTTGG | 83860 |
rs4749308 | snp | A/G | 0.158962 | 0.232835 | intron-variant | TAF3 | GRCh38.p7 | 10:7847011 | tttcatttgaataca[A/G]ttgaaatttagaatt | 83860 |
rs4749312 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | TAF3 | GRCh38.p7 | 10:7852236 | attacagacgcCTGG[C/T]ACCTAGCTAGCCACT | 83860 |
rs4749315 | snp | C/T | 0.105569 | 0.204058 | intron-variant | TAF3 | GRCh38.p7 | 10:7856222 | GGGCGCAGTGGCTCA[C/T]GCCAGCACTTTGGGA | 83860 |
rs4749316 | snp | A/G | 0.49949 | 0.0159663 | intron-variant | TAF3 | GRCh38.p7 | 10:7865609 | ACAGGCCTGCGTGTC[A/G]CTGGCTTTAGCAGCC | 83860 |
rs4749317 | snp | A/T | 0.35574 | 0.226537 | intron-variant | TAF3 | GRCh38.p7 | 10:7866934 | GATCAATGTGCAATT[A/T]AAATTCCAAACTGAG | 83860 |
rs4749329 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | TAF3 | GRCh38.p7 | 10:7893026 | GGTTTCTCCATGTTG[A/G]TCAGGCTGGTCTCCA | 83860 |
rs4749339 | snp | G/T | 0.324855 | 0.23853 | intron-variant | TAF3 | GRCh38.p7 | 10:7907303 | ATTGTGATGCCAGAT[G/T]AGGTCTTTGAAATCC | 83860 |
rs4749342 | snp | A/G | 0.342582 | 0.232225 | intron-variant | TAF3 | GRCh38.p7 | 10:7911504 | GCTGGTGTACTTGGT[A/G]TGATAGTACATACCT | 83860 |
rs4749343 | snp | C/T | 0.342358 | 0.232314 | intron-variant | TAF3 | GRCh38.p7 | 10:7911560 | CTTAGGGAATATCCT[C/T]AGCTTTGTTTGATAG | 83860 |
rs4749347 | snp | C/T | 0.455383 | 0.142541 | intron-variant | TAF3 | GRCh38.p7 | 10:7912847 | TTTTCCTTTCTGAAT[C/T]GGACCCCGGAATCCC | 83860 |
rs4749348 | snp | C/T | 0.438946 | 0.163706 | intron-variant | TAF3 | GRCh38.p7 | 10:7914334 | ATTGGCTTATGTTAA[C/T]CCCTTGGGGGAGATA | 83860 |
rs4749351 | snp | A/T | 0.326976 | 0.237854 | intron-variant | TAF3 | GRCh38.p7 | 10:7917544 | tggaatggacttggg[A/T]tttttttctaatcta | 83860 |
rs4749353 | snp | C/T | 0.492775 | 0.059668 | intron-variant | TAF3 | GRCh38.p7 | 10:7919101 | GTGCATTTCAGAGGG[C/T]ACAGAATCTGAAAAA | 83860 |
rs4749358 | snp | A/C | 0.492679 | 0.0600586 | intron-variant | TAF3 | GRCh38.p7 | 10:7924546 | TATGTGGGCATGTCT[A/C]CCATTTTCTCTTTAA | 83860 |
rs4749359 | snp | A/G | 0.494733 | 0.0510469 | intron-variant | TAF3 | GRCh38.p7 | 10:7926141 | CTTTTGATGTTACTG[A/G]TCTGACTGAGAAAGG | 83860 |
rs4749360 | snp | A/C | 0.49621 | 0.0433651 | intron-variant | TAF3 | GRCh38.p7 | 10:7926279 | ACTTTTTTTTTATTA[A/C]GCCAAGGAAGAGGTG | 83860 |
rs4749361 | snp | G/T | 0.488545 | 0.074807 | intron-variant | TAF3 | GRCh38.p7 | 10:7926338 | GTGAATGTTCAGTAA[G/T]TCCTGCCATACTTGA | 83860 |
rs4749362 | snp | A/G | 0.440609 | 0.161766 | intron-variant | TAF3 | GRCh38.p7 | 10:7926434 | TCAAGTATCTGATTA[A/G]GAAAAAGTATTACCA | 83860 |
rs4749378 | snp | A/G | 0.368119 | 0.220336 | intron-variant | TAF3 | GRCh38.p7 | 10:7939477 | TGTCCAGCGACTCAC[A/G]CTTAAACACCCAGTA | 83860 |
rs4749393 | snp | A/C | 0.317451 | 0.240729 | intron-variant | TAF3 | GRCh38.p7 | 10:7944988 | TATTAGTCTCTACCT[A/C]GAAATATGGGCAGCA | 83860 |
rs4749399 | snp | A/T | 0.318174 | 0.240525 | intron-variant | TAF3 | GRCh38.p7 | 10:7950090 | CTGTAATGGTGGTTT[A/T]GCAGCAGAAGGCAGA | 83860 |
rs4749400 | snp | A/G | 0.488363 | 0.0753851 | intron-variant | TAF3 | GRCh38.p7 | 10:7950415 | CAGAAAGTTCCTCAC[A/G]TGGCTAGTTCTTTGA | 83860 |
rs4749442 | snp | C/T | 0.36606 | 0.221428 | intron-variant | TAF3 | GRCh38.p7 | 10:7986425 | GATGAGACCAGTGCC[C/T]CCATTTTCAAGCCAT | 83860 |
rs4749477 | snp | G/T | 0.240765 | 0.249829 | intron-variant | TAF3 | GRCh38.p7 | 10:8003459 | gatctttataagtca[G/T]tgaaccagtattttc | 83860 |
rs4749478 | snp | C/T | 0.422158 | 0.181278 | intron-variant | TAF3 | GRCh38.p7 | 10:8004199 | gggattacaggtctg[C/T]gccatcacacccagc | 83860 |
rs5783000 | in-del | -/A | 0.496517 | 0.0415876 | intron-variant | TAF3 | GRCh38.p7 | 10:7822244 | TCTGAAATCATGGTT[-/A]AAAAAAAAAAAAAAA | 83860 |
rs5783006 | in-del | -/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971453 | TATACATATATGGTG[-/T]TTTTTTTTTTTTTTA | 83860 |
rs5783007 | in-del | -/A | 0.47709 | 0.104548 | intron-variant | TAF3 | GRCh38.p7 | 10:7979363 | AATGAAAAAAAAATG[-/A]AAAAAAAAAAAAAGG | 83860 |
rs6602272 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7831506 | atgtgccaccacgcc[C/T]ggctaatttttgtat | 83860 |
rs6602273 | snp | A/G | 0.18325 | 0.240924 | intron-variant | TAF3 | GRCh38.p7 | 10:7832026 | tcacctcaaatgcct[A/G]tcgttttttgtggag | 83860 |
rs6602275 | snp | C/T | 0.11228 | 0.208646 | intron-variant | TAF3 | GRCh38.p7 | 10:7861770 | TTAACTAGGATGTGC[C/T]TAGGTGTGGTTTTCT | 83860 |
rs6602280 | snp | A/G | 0.177503 | 0.239258 | intron-variant | TAF3 | GRCh38.p7 | 10:7999596 | CAAGTAGCTGGGATT[A/G]TAAGTGGATACCACC | 83860 |
rs6602281 | snp | C/T | 0.279461 | 0.248258 | intron-variant | TAF3 | GRCh38.p7 | 10:7999708 | GCAGTCCTCCTGCCT[C/T]GGCCTGCCAAAGTGC | 83860 |
rs7067840 | snp | C/T | 0.360842 | 0.224085 | intron-variant | TAF3 | GRCh38.p7 | 10:7841932 | ACATGACACGAACCT[C/T]GTACCCAGGGCAGAC | 83860 |
rs7069058 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7902433 | tgtcttaaaaaaaaa[A/T]aataaaaaaagaaTC | 83860 |
rs7069059 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7902436 | cttaaaaaaaaataa[G/T]aaaaaaagaaTCTTT | 83860 |
rs7069192 | snp | C/T | 0.182614 | 0.240747 | intron-variant | TAF3 | GRCh38.p7 | 10:7902506 | TGCGTGTGGTtgttt[C/T]ctcatgacgaaactc | 83860 |
rs7070208 | snp | C/G | 0.254302 | 0.249963 | intron-variant | TAF3 | GRCh38.p7 | 10:7824305 | ATTTGATTTGCTTTT[C/G]ACTTTGTTTCAGATG | 83860 |
rs7073198 | snp | C/G | 0.182296 | 0.240658 | intron-variant | TAF3 | GRCh38.p7 | 10:8013652 | GGTTAACAGTATAAA[C/G]TAATCATTCTGATCT | 83860 |
rs7073640 | snp | C/G | 0.409382 | 0.192607 | intron-variant | TAF3 | GRCh38.p7 | 10:8014015 | GCAAAACCCAAGAGT[C/G]CTTAGACTATTGTTA | 83860 |
rs7074397 | snp | C/T | 0.279726 | 0.248226 | intron-variant | TAF3 | GRCh38.p7 | 10:7994053 | tttctctgctccccc[C/T]accccttcttctctc | 83860 |
rs7076015 | snp | A/T | 0.350982 | 0.228698 | intron-variant | TAF3 | GRCh38.p7 | 10:7921786 | TTGTTAGTTGAATAT[A/T]GTAGAAGAAAATTTG | 83860 |
rs7076085 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | TAF3 | GRCh38.p7 | 10:7864309 | ttacttttttcagaa[A/G]ttaattgacagatat | 83860 |
rs7076314 | snp | C/T | 0.488726 | 0.0742286 | intron-variant | TAF3 | GRCh38.p7 | 10:7922013 | ATCACAAATTTTTGT[C/T]AGACTTGAATTGGAA | 83860 |
rs7076815 | snp | A/C | 0.493247 | 0.0577133 | intron-variant | TAF3 | GRCh38.p7 | 10:7915260 | GCTCCCCAGCCTTTT[A/C]TGAAGAACCTGCGCT | 83860 |
rs7076829 | snp | A/T | 0.371987 | 0.218218 | intron-variant | TAF3 | GRCh38.p7 | 10:7864783 | ttaacattatctttc[A/T]agaagtaaatgtttc | 83860 |
rs7078361 | snp | A/G | 0.325563 | 0.238307 | intron-variant | TAF3 | GRCh38.p7 | 10:7832029 | cctcaaatgcctatc[A/G]ttttttgtggagaga | 83860 |
rs7078878 | snp | G/T | 0.488846 | 0.0738428 | intron-variant | TAF3 | GRCh38.p7 | 10:7967190 | CTTCACGTGGTGAGG[G/T]GTTTGTTGTTAGAGA | 83860 |
rs7080680 | snp | C/T | 0.487746 | 0.0773096 | intron-variant | TAF3 | GRCh38.p7 | 10:7915419 | ggaggccgagacggg[C/T]ggatcacgaggtcag | 83860 |
rs7080906 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7907670 | CTTTAATGCCTCATC[A/C]ATTGCCCTGCCCATT | 83860 |
rs7083651 | snp | A/G | 0.107694 | 0.205546 | intron-variant | TAF3 | GRCh38.p7 | 10:7999512 | cccaggctggagtgc[A/G]aaggtgtgatcttgg | 83860 |
rs7087039 | snp | A/G | 0.441295 | 0.160954 | intron-variant | TAF3 | GRCh38.p7 | 10:7981433 | ATCATGCATGGTCAT[A/G]TTTTCTCTAATAAAT | 83860 |
rs7087694 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999809 | TAGGAGGTTTTCTCT[C/T]CCCCCTCCTTTGACC | 83860 |
rs7092822 | snp | A/G | 0.16028 | 0.233346 | intron-variant | TAF3 | GRCh38.p7 | 10:7973605 | TAAAATGAAACCCAC[A/G]TTATCTACCCTACAT | 83860 |
rs7093390 | snp | C/T | 0.191775 | 0.243125 | intron-variant | TAF3 | GRCh38.p7 | 10:8010403 | GTGGTACTGAAATCT[C/T]ACATTGAATTTCTTG | 83860 |
rs7093757 | snp | A/T | 0.492918 | 0.0590819 | intron-variant | TAF3 | GRCh38.p7 | 10:7966952 | CTCTTATTTCCATTT[A/T]AAAAATCATTTTATT | 83860 |
rs7096633 | snp | A/G | 0.108402 | 0.206034 | intron-variant | TAF3 | GRCh38.p7 | 10:7976144 | GTGTTCTCTTCTGAC[A/G]AACAGGTCAGATCTT | 83860 |
rs7098551 | snp | A/C | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820019 | ACAGTTCCCTTTGTG[A/C]GCTAGCATTTTGCTT | 83860 |
rs7099061 | snp | A/G | 0.384017 | 0.211044 | intron-variant | TAF3 | GRCh38.p7 | 10:7823855 | gaccaggttggtctc[A/G]aacccttgaccttgt | 83860 |
rs7099384 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7823438 | gagttcaaaaccagc[C/T]tgagcaacatagcaa | 83860 |
rs7099564 | snp | G/T | 0.342134 | 0.232404 | intron-variant | TAF3 | GRCh38.p7 | 10:7912065 | TTTTATGTCATTGTA[G/T]TTTGGGAGATATTTT | 83860 |
rs7099769 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823706 | gtggcacgatctcgg[C/T]tcactgcaacctccg | 83860 |
rs7101294 | snp | A/G | 0.498525 | 0.0271165 | intron-variant | TAF3 | GRCh38.p7 | 10:7980910 | GGTCATTTTGAGCAA[A/G]TGTAGGTAGAATTGG | 83860 |
rs7478482 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837779 | aggctgcagtgagcc[A/C]ctgcactccagcctg | 83860 |
rs7893610 | snp | C/T | 0.226188 | 0.248863 | intron-variant | TAF3 | GRCh38.p7 | 10:7995531 | TTACCTGAATATTAA[C/T]GCCCTTTTAGAGATT | 83860 |
rs7894336 | snp | C/T | 0.499713 | 0.0119774 | intron-variant | TAF3 | GRCh38.p7 | 10:7984646 | TATTTATGACCACCT[C/T]TTTAGATATGATTTG | 83860 |
rs7894908 | snp | A/G | 0.297128 | 0.245518 | intron-variant | TAF3 | GRCh38.p7 | 10:7993234 | cccaggctggaatgc[A/G]gtggtacgatcataa | 83860 |
rs7895109 | snp | A/G | 0.277867 | 0.248442 | intron-variant | TAF3 | GRCh38.p7 | 10:8000433 | TTTTCTTTTTTTTAT[A/G]CAAGTTATGTTTGTT | 83860 |
rs7898426 | snp | A/G | 0.300926 | 0.244758 | intron-variant | TAF3 | GRCh38.p7 | 10:7861023 | CTGGAGTGCAGTGGC[A/G]CCATCTCGGCTCACT | 83860 |
rs7900324 | snp | A/G | 0.493107 | 0.0583 | intron-variant | TAF3 | GRCh38.p7 | 10:7936997 | atttcagattcctct[A/G]tatctttttatggct | 83860 |
rs7901324 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7827190 | CGTGGACCTCACGGC[A/G]TCACTGAGACATGAC | 83860 |
rs7902234 | snp | A/G | 0.139903 | 0.224452 | intron-variant | TAF3 | GRCh38.p7 | 10:7891594 | TGTTTTATTTTCCCT[A/G]TTTTCTGTCTTTACC | 83860 |
rs7902732 | snp | C/T | 0.285519 | 0.247464 | intron-variant | TAF3 | GRCh38.p7 | 10:7861185 | TAGCCAGGGTGGTCT[C/T]GATCTCCTGACCTCG | 83860 |
rs7905267 | snp | C/T | 0.491473 | 0.0647364 | intron-variant | TAF3 | GRCh38.p7 | 10:7915511 | agccgggcatggtgg[C/T]gcgcgcccgtagtcc | 83860 |
rs7906959 | snp | C/T | 0.299664 | 0.245017 | intron-variant | TAF3 | GRCh38.p7 | 10:7845801 | CTGATTTTTAACTTA[C/T]GTGAATAGCATTGCT | 83860 |
rs7907669 | snp | C/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7980454 | TAACATTCCTGGAAA[C/G]TGTATTCTAAAGGAG | 83860 |
rs7908263 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7840817 | CTGCTTACAGCCACA[C/T]AGAACTTTGCTATTT | 83860 |
rs7909825 | snp | A/G | 0.438666 | 0.164028 | intron-variant | TAF3 | GRCh38.p7 | 10:7896164 | GAACCTTGTTCTATT[A/G]TGTATGCTAGTAAGG | 83860 |
rs7913604 | snp | C/T | 0.318896 | 0.240319 | intron-variant | TAF3 | GRCh38.p7 | 10:8004299 | gcgatccacccacct[C/T]ggcctcccaaagtgc | 83860 |
rs7915234 | snp | C/T | 0.438806 | 0.163867 | intron-variant | TAF3 | GRCh38.p7 | 10:7897152 | tgaagagatcaggcc[C/T]gcttggcaagtctcg | 83860 |
rs7916205 | snp | A/G | 0.498084 | 0.0308911 | intron-variant | TAF3 | GRCh38.p7 | 10:7915500 | atacaaaaattagcc[A/G]ggcatggtggtgcgc | 83860 |
rs7916621 | snp | A/G | 0.493201 | 0.0579089 | intron-variant | TAF3 | GRCh38.p7 | 10:7915808 | acatggtgaaatctc[A/G]tctctactaaaaata | 83860 |
rs7917461 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7998265 | TATATATATATATAT[A/G]TATATATATATATAT | 83860 |
rs7921606 | snp | C/T | 0.357451 | 0.225731 | intron-variant | TAF3 | GRCh38.p7 | 10:7843883 | TTACTCTTTGTGGAC[C/T]TCAAATTTTGCAGTA | 83860 |
rs7922353 | snp | A/C | 0.426966 | 0.176587 | intron-variant | TAF3 | GRCh38.p7 | 10:7962619 | GTTTCACCTTCATCT[A/C]TTTGTCATCTGACCC | 83860 |
rs9633771 | snp | A/C | 0.410905 | 0.191336 | intron-variant | TAF3 | GRCh38.p7 | 10:7960307 | TTCTGATAGCAAAAG[A/C]GAGGGAGGGAGGGAA | 83860 |
rs9645598 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7838808 | CTCTCTCTTGGCCCT[C/T]TCAGATACCTTCCTG | 83860 |
rs9645599 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838856 | CTGGAGTTCCAGGGT[C/T]TGGGGAACGTTCCTT | 83860 |
rs9664026 | snp | C/T | 0.36315 | 0.222928 | intron-variant | TAF3 | GRCh38.p7 | 10:7836622 | tgttatccatctcag[C/T]tggtggcaccatctc | 83860 |
rs9787560 | snp | A/G | 0.350109 | 0.229081 | intron-variant | TAF3 | GRCh38.p7 | 10:7831695 | GTTGCATCTTTGGCC[A/G]GTGGCAGCTTCTTCA | 83860 |
rs10430789 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | TAF3 | GRCh38.p7 | 10:7959165 | ACACACACACACACA[A/C]AAAAAGTTTCAGGCT | 83860 |
rs10508336 | snp | A/G | 0.192088 | 0.2432 | intron-variant | TAF3 | GRCh38.p7 | 10:7834867 | TTCTTTCATTTTACC[A/G]TGTGTATCTTGTCAG | 83860 |
rs10508337 | snp | A/G | 0.113334 | 0.209338 | intron-variant | TAF3 | GRCh38.p7 | 10:7835432 | TATGGGAACTTGCTC[A/G]CTGAGATTTTTTGTT | 83860 |
rs10508338 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | TAF3 | GRCh38.p7 | 10:7893798 | ATTTTATCAGCTATT[C/T]TCTTATCTTTATTAG | 83860 |
rs10508339 | snp | A/G | 0.342806 | 0.232136 | intron-variant | TAF3 | GRCh38.p7 | 10:7909482 | TCACTGTGCCATTGG[A/G]TAAACTAGTGTCATT | 83860 |
rs10737026 | snp | A/G | 0.494057 | 0.0541878 | intron-variant | TAF3 | GRCh38.p7 | 10:7954392 | GTGCACTCCATAGGC[A/G]AATGAGTGAATTAGT | 83860 |
rs10752118 | snp | C/T | 0.455383 | 0.142541 | intron-variant | TAF3 | GRCh38.p7 | 10:7871095 | TACACTGTAGTCAGT[C/T]GTTTAATATACTTGT | 83860 |
rs10752119 | snp | A/G | 0.492386 | 0.0612297 | intron-variant | TAF3 | GRCh38.p7 | 10:7892270 | AAAGATCAATAAGCA[A/G]ATTTAGCATGTGCTG | 83860 |
rs10752120 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | TAF3 | GRCh38.p7 | 10:7897871 | TCACTTTGGTGCCCA[A/G]GCTGGTTTTCAACTG | 83860 |
rs10752121 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7902015 | TCGGAACCACTGAGA[A/G]TACTGGCAGACACTA | 83860 |
rs10752122 | snp | A/C | 0.465368 | 0.126951 | intron-variant | TAF3 | GRCh38.p7 | 10:7969460 | AAATGTTTTATTAAA[A/C]TTTTGGTTTCTGTGT | 83860 |
rs10752123 | snp | A/G | 0.499767 | 0.0107802 | intron-variant | TAF3 | GRCh38.p7 | 10:8004826 | GGATTGGTATCTTTC[A/G]TCAGTTCTGTAAAAG | 83860 |
rs10752124 | snp | C/T | 0.493748 | 0.0555599 | intron-variant | TAF3 | GRCh38.p7 | 10:8004957 | TCTTAGGCTATGCTC[C/T]GAAAATTTATTTTGT | 83860 |
rs10795571 | snp | C/G | 0.349452 | 0.229367 | intron-variant | TAF3 | GRCh38.p7 | 10:7900459 | TGACTGCTACTCCTC[C/G]GTGGATGGCTGGAGA | 83860 |
rs10795572 | snp | A/C | 0.490231 | 0.0692021 | intron-variant | TAF3 | GRCh38.p7 | 10:7904008 | TGTCTGAGAAGTTTC[A/C]CGGTGCGTCTGAGTT | 83860 |
rs10795573 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | TAF3 | GRCh38.p7 | 10:7904037 | TTGGAGCAGAGTCCA[A/G]TGTACTTGGAAACAA | 83860 |
rs10795574 | snp | A/G | 0.440884 | 0.161442 | intron-variant | TAF3 | GRCh38.p7 | 10:7906174 | TTCTCCTCCAACTCA[A/G]CTTTCCTTTATTTTT | 83860 |
rs10795576 | snp | A/G | 0.497855 | 0.0326773 | intron-variant | TAF3 | GRCh38.p7 | 10:7913406 | GGCTTGATCCAGGCA[A/G]TACTTTGCAGCCTTT | 83860 |
rs10795577 | snp | A/G | 0.178144 | 0.239451 | intron-variant | TAF3 | GRCh38.p7 | 10:7941092 | TAAGAGTAAAAGTTA[A/G]GTTGGAAACATAGAG | 83860 |
rs10795578 | snp | A/G | 0.493107 | 0.0583 | intron-variant | TAF3 | GRCh38.p7 | 10:7941569 | AAAGGAGGAAGAGCC[A/G]CTGCCCTCTGCTTCG | 83860 |
rs10795579 | snp | A/G | 0.460477 | 0.134905 | intron-variant | TAF3 | GRCh38.p7 | 10:7943026 | TACAGTTGCCGTCCA[A/G]TCCAGTTTCTTTCTG | 83860 |
rs10795580 | snp | A/T | 0.498459 | 0.0277128 | intron-variant | TAF3 | GRCh38.p7 | 10:7952921 | ATATTTTATAAGGAG[A/T]TGTCAATGGAATTAT | 83860 |
rs10795582 | snp | C/T | 0.441158 | 0.161117 | intron-variant | TAF3 | GRCh38.p7 | 10:7960085 | AAAGACCCGTTATCC[C/T]GCCTAAGCCAAACCT | 83860 |
rs10795583 | snp | C/G | 0.466459 | 0.125082 | missense | TAF3 | GRCh38.p7 | 10:7965596 | GAGGAGAAAGAGAAG[C/G]TGAAGGAGAAAGAAA | 83860 |
rs10795584 | snp | A/G | 0.499053 | 0.0217445 | intron-variant | TAF3 | GRCh38.p7 | 10:7977161 | TTAACTCAGTTTGTG[A/G]GAGTGGGAGAGTAGG | 83860 |
rs10795586 | snp | A/G | 0.246485 | 0.249975 | intron-variant | TAF3 | GRCh38.p7 | 10:8013913 | TGAAGCATCCACTGA[A/G]TAGATTCCTGCCTTT | 83860 |
rs10905235 | snp | A/G | 0.161924 | 0.233971 | intron-variant | TAF3 | GRCh38.p7 | 10:7842267 | CAACCTCTGCCTCCC[A/G]GGCTCAAGCAGTCCT | 83860 |
rs10905236 | snp | A/T | 0.161267 | 0.233723 | intron-variant | TAF3 | GRCh38.p7 | 10:7842613 | GATGATACCTAATGG[A/T]CACTATTGTCATGTC | 83860 |
rs10905237 | snp | G/T | 0.378174 | 0.214642 | intron-variant | TAF3 | GRCh38.p7 | 10:7847988 | GTGTCCAGGCTGATC[G/T]CAAACTCCTGACCTC | 83860 |
rs10905238 | snp | G/T | 0.108402 | 0.206034 | intron-variant | TAF3 | GRCh38.p7 | 10:7852119 | AGACGGGGTCTCACT[G/T]TGTTGCCCAGGCTGG | 83860 |
rs10905239 | snp | C/T | 0.350764 | 0.228794 | intron-variant | TAF3 | GRCh38.p7 | 10:7857268 | TTCACAATGGAACAG[C/T]CACAGCTCACTTATA | 83860 |
rs10905240 | snp | A/G | 0.431177 | 0.172264 | intron-variant | TAF3 | GRCh38.p7 | 10:7866589 | ATCTACTGAGGGAGC[A/G]TGGCGTAAGATGAAG | 83860 |
rs10905241 | snp | A/T | 0.43978 | 0.162738 | intron-variant | TAF3 | GRCh38.p7 | 10:7886426 | TTTGCCTTTATTTTT[A/T]AATCATGAATATGTA | 83860 |
rs10905242 | snp | C/T | 0.486266 | 0.0817214 | intron-variant | TAF3 | GRCh38.p7 | 10:7896867 | AGATGTCAGCCCAGT[C/T]GAGCCCAGATGTCAG | 83860 |
rs10905243 | snp | A/G | 0.343254 | 0.231956 | intron-variant | TAF3 | GRCh38.p7 | 10:7906499 | TCTTTCGGAGGAGAA[A/G]AGCCAGAAAAATACA | 83860 |
rs10905244 | snp | C/T | 0.438526 | 0.164189 | intron-variant | TAF3 | GRCh38.p7 | 10:7911902 | CTAGCTTGCTTTACT[C/T]GTTCGCTTCATTTTT | 83860 |
rs10905245 | snp | A/G | 0.493201 | 0.0579089 | intron-variant | TAF3 | GRCh38.p7 | 10:7914710 | TTTCTGAGGGATGGG[A/G]TAGTAAGTGCTTCCT | 83860 |
rs10905246 | snp | G/T | 0.498084 | 0.0308911 | intron-variant | TAF3 | GRCh38.p7 | 10:7914739 | CTAAGCTTTTATTCT[G/T]GAGAACTCAAATATG | 83860 |
rs10905247 | snp | A/G | 0.438806 | 0.163867 | intron-variant | TAF3 | GRCh38.p7 | 10:7915132 | TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTA | 83860 |
rs10905248 | snp | C/T | 0.440609 | 0.161766 | intron-variant | TAF3 | GRCh38.p7 | 10:7918537 | GAGCTGGGAGCATGA[C/T]GGGAATGTGGGTCCT | 83860 |
rs10905249 | snp | A/G | 0.440333 | 0.16209 | intron-variant | TAF3 | GRCh38.p7 | 10:7918607 | TGCTGATATAGAAGC[A/G]GATGCACCAGGGGGC | 83860 |
rs10905250 | snp | G/T | 0.439918 | 0.162576 | intron-variant | TAF3 | GRCh38.p7 | 10:7919027 | AGGTTTAACAGGAAG[G/T]TGAAGGGAACAGTTA | 83860 |
rs10905251 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | TAF3 | GRCh38.p7 | 10:7919960 | TCAAATAATTTAAAA[C/T]TTAGGCTGGGTGTGG | 83860 |
rs10905252 | snp | A/G | 0.494143 | 0.0537956 | intron-variant | TAF3 | GRCh38.p7 | 10:7922254 | GCACTAATGTTAATT[A/G]TGAAAAGGTTTTAGA | 83860 |
rs10905253 | snp | C/T | 0.495999 | 0.0445491 | intron-variant | TAF3 | GRCh38.p7 | 10:7925561 | GTAATCCCAGCACTT[C/T]GGGAGGCCAGGGCAG | 83860 |
rs10905254 | snp | C/T | 0.494609 | 0.0516363 | intron-variant | TAF3 | GRCh38.p7 | 10:7925671 | TTAGGCATGATGGTG[C/T]GCCTGTATTCCCAGC | 83860 |
rs10905257 | snp | A/C | 0.492966 | 0.0588865 | intron-variant | TAF3 | GRCh38.p7 | 10:7930410 | AGTATATAGACTCGT[A/C]CAGCCCTATTTCTAG | 83860 |
rs10905258 | snp | A/G | 0.124837 | 0.216412 | intron-variant | TAF3 | GRCh38.p7 | 10:7949877 | TCAAGTTCACCCATC[A/G]GCAGGCAGTGACTGC | 83860 |
rs10905259 | snp | C/G | 0.48666 | 0.0805725 | intron-variant | TAF3 | GRCh38.p7 | 10:7954712 | CTCCCTAGTGAGATT[C/G]AGAGTGCACTCCATA | 83860 |
rs10905260 | snp | A/G | 0.489024 | 0.0732638 | intron-variant | TAF3 | GRCh38.p7 | 10:7956018 | TTAGGGTAAAGGATC[A/G]TGATGTCTACAACTT | 83860 |
rs10905261 | snp | C/G | 0.449218 | 0.151037 | intron-variant | TAF3 | GRCh38.p7 | 10:7960861 | GTAAAATAGATAACC[C/G]CAGGCATAACTCTTC | 83860 |
rs10905262 | snp | A/G | 0.440884 | 0.161442 | intron-variant | TAF3 | GRCh38.p7 | 10:7963648 | GGAACATCACACATC[A/G]GCACCTGTTGGGAGG | 83860 |
rs10905263 | snp | A/G | 0.440746 | 0.161604 | intron-variant | TAF3 | GRCh38.p7 | 10:7963687 | TGGGGGAGGGATAGC[A/G]TTAGGAGAAATACCT | 83860 |
rs10905264 | snp | A/T | 0.492966 | 0.0588865 | intron-variant | TAF3 | GRCh38.p7 | 10:7966405 | ATCTCAGTAAGTCAG[A/T]CTTCATTTCATAGCA | 83860 |
rs10905265 | snp | A/G | 0.132066 | 0.220435 | intron-variant | TAF3 | GRCh38.p7 | 10:7998223 | TTTCTTTTACTACTC[A/G]GAAAATCTGAGTGAG | 83860 |
rs10905266 | snp | C/T | 0.377582 | 0.214995 | intron-variant | TAF3 | GRCh38.p7 | 10:8006281 | CTTGGGAGGCTAAGG[C/T]GGGAGAATCACTTGA | 83860 |
rs10905267 | snp | C/T | 0.244776 | 0.249945 | intron-variant | TAF3 | GRCh38.p7 | 10:8014532 | GCTTGACTTTGATTT[C/T]GGGTAAACATGTCAT | 83860 |
rs11255374 | snp | A/G | 0.252983 | 0.249982 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817193 | GTTCAACATTATCAA[A/G]TAGCTACAAAATAAT | 83860 |
rs11255375 | snp | A/T | 0.282369 | 0.247896 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817575 | CGACCTGCAGGCTGA[A/T]TCTAGACTAACCGTG | 83860 |
rs11255376 | snp | G/T | 0.399611 | 0.200291 | upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818475 | CGCGCTCGGCATTCG[G/T]CTTATGCTGCCTCGC | 83860 |
rs11255377 | snp | C/G | 0.349671 | 0.229272 | intron-variant | TAF3 | GRCh38.p7 | 10:7822281 | CGAAGGGGACGGGGA[C/G]AGGGTTAGAAACTAC | 83860 |
rs11255378 | snp | C/T | 0.350109 | 0.229081 | intron-variant | TAF3 | GRCh38.p7 | 10:7822294 | GACAGGGTTAGAAAC[C/T]ACCAGGTTTTGGTTT | 83860 |
rs11255379 | snp | C/G | 0.350109 | 0.229081 | intron-variant | TAF3 | GRCh38.p7 | 10:7822527 | AAGTATGTGGAGTTA[C/G]AAGTCAGTCTCCTGC | 83860 |
rs11255380 | snp | C/G | 0.350109 | 0.229081 | intron-variant | TAF3 | GRCh38.p7 | 10:7822657 | TGCGTCCAATTCTAG[C/G]AATATTTGGATTCTT | 83860 |
rs11255381 | snp | G/T | 0.350982 | 0.228698 | intron-variant | TAF3 | GRCh38.p7 | 10:7823862 | TTGGTCTCGAACCCT[G/T]GACCTTGTGATCCGC | 83860 |
rs11255382 | snp | A/G | 0.34989 | 0.229177 | intron-variant | TAF3 | GRCh38.p7 | 10:7825663 | gttgtagcctgtgtc[A/G]ggatttcgttgtgtg | 83860 |
rs11255383 | snp | C/G | 0.34989 | 0.229177 | intron-variant | TAF3 | GRCh38.p7 | 10:7825969 | CTTCCTATCAGCAGT[C/G]CCCAAGGGTTCCAAT | 83860 |
rs11255384 | snp | C/T | 0.34989 | 0.229177 | intron-variant | TAF3 | GRCh38.p7 | 10:7825970 | TTCCTATCAGCAGTG[C/T]CCAAGGGTTCCAATT | 83860 |
rs11255385 | snp | G/T | 0.34989 | 0.229177 | intron-variant | TAF3 | GRCh38.p7 | 10:7826085 | TTGGCATAAGTTGTT[G/T]TACAGTCTGTGTGTC | 83860 |
rs11255386 | snp | A/T | 0.350109 | 0.229081 | intron-variant | TAF3 | GRCh38.p7 | 10:7826132 | AAAAACTGGACAGCT[A/T]CTGGACCTAAGTGGT | 83860 |
rs11255387 | snp | C/T | 0.350109 | 0.229081 | intron-variant | TAF3 | GRCh38.p7 | 10:7826200 | GCTCTGGATCTTAGC[C/T]GCAGTGGGTTCTACT | 83860 |
rs11255388 | snp | A/G | 0.157972 | 0.232445 | intron-variant | TAF3 | GRCh38.p7 | 10:7827409 | GGTGTGATGGCTTAT[A/G]CACTTTGGGAGGCTG | 83860 |
rs11255389 | snp | C/T | 0.243061 | 0.249904 | intron-variant | TAF3 | GRCh38.p7 | 10:7829795 | TCACTGTGCGTAGCC[C/T]GCCCTTAAGGAATGG | 83860 |
rs11255391 | snp | C/T | 0.113334 | 0.209338 | intron-variant | TAF3 | GRCh38.p7 | 10:7831477 | CAGCCTCTCCAGTAG[C/T]TGGGATTACAGGCAT | 83860 |
rs11255393 | snp | C/G | 0.350327 | 0.228986 | intron-variant | TAF3 | GRCh38.p7 | 10:7834235 | CAGTTTTGCTTTTGT[C/G]ACCCTGCGCTTTTGG | 83860 |
rs11255394 | snp | A/G | 0.397633 | 0.201754 | intron-variant | TAF3 | GRCh38.p7 | 10:7834282 | TAATTGCCCAGACCA[A/G]TGTCTTACAGTTTTT | 83860 |
rs11255395 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7834660 | TTTATGTTACATCCA[C/T]AAATACTGTCATCCA | 83860 |
rs11255396 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838359 | TACCAAGCCAGtttt[G/T]tttttttttgttgtt | 83860 |
rs11255397 | snp | C/G | 0.299158 | 0.245119 | intron-variant | TAF3 | GRCh38.p7 | 10:7843097 | TTCCCATGGAACTGC[C/G]CAGAAGCTGCACAGG | 83860 |
rs11255398 | snp | A/G | 0.299664 | 0.245017 | intron-variant | TAF3 | GRCh38.p7 | 10:7845318 | TCTTTGTGTGTGTGC[A/G]TGTGTGTGTGCACAC | 83860 |
rs11255399 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7845467 | GGTAGGGGTGAACCC[A/G]AAGTGCATAAAATGC | 83860 |
rs11255400 | snp | A/G | 0.167809 | 0.236103 | intron-variant | TAF3 | GRCh38.p7 | 10:7845658 | CTGATCAGATTTAGA[A/G]TGAAGGTGAGAGGTC | 83860 |
rs11255401 | snp | C/T | 0.178465 | 0.239547 | intron-variant | TAF3 | GRCh38.p7 | 10:7846432 | TTTTAGTTCTTCTGG[C/T]ACCAACATTTAACAT | 83860 |
rs11255402 | snp | A/G | 0.106987 | 0.205054 | intron-variant | TAF3 | GRCh38.p7 | 10:7847574 | TCAGCCTTCTGGGTA[A/G]CTGGAACTACAGGCA | 83860 |
rs11255403 | snp | C/T | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7851001 | AGTGAACAAAGCAGA[C/T]AAACAGTCTCTGCTT | 83860 |
rs11255404 | snp | A/G | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7851160 | TAAAAATGCTAGAGT[A/G]TGGGAAGGAAAGTTG | 83860 |
rs11255405 | snp | A/G | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7852295 | CTTTTCACATTTTAA[A/G]TTTTCTCTCAAATGT | 83860 |
rs11255406 | snp | A/G | 0.282369 | 0.247896 | intron-variant | TAF3 | GRCh38.p7 | 10:7856381 | GCTACTCGGGAGGCC[A/G]AGGCAGGAGAATCGC | 83860 |
rs11255407 | snp | A/G | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7856539 | AAAAATTATAGAACC[A/G]GTCCAGGAAGCCTAA | 83860 |
rs11255408 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857227 | TTCTGAATACTGGAA[A/G/T]AATATTTCCTCAGCT | 83860 |
rs11255409 | snp | A/G | 0.356597 | 0.226135 | intron-variant | TAF3 | GRCh38.p7 | 10:7859240 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 83860 |
rs11255411 | snp | C/T | 0.105924 | 0.204309 | intron-variant | TAF3 | GRCh38.p7 | 10:7862279 | AGTTTTCTGTTTTTT[C/T]ACATGTCTAATAATT | 83860 |
rs11255412 | snp | A/G | 0.301177 | 0.244706 | intron-variant | TAF3 | GRCh38.p7 | 10:7862424 | CAAGCTGTTTTTCCT[A/G]TGATGGGCAGCAGCA | 83860 |
rs11255413 | snp | A/G | 0.301429 | 0.244653 | intron-variant | TAF3 | GRCh38.p7 | 10:7863388 | GGTTGAGGCAGGCAG[A/G]TCACCTGAGTTCAGG | 83860 |
rs11255414 | snp | A/G | 0.356811 | 0.226034 | intron-variant | TAF3 | GRCh38.p7 | 10:7863440 | GGATGGTGAAACCCC[A/G]TCTCTACTGAAAATA | 83860 |
rs11255415 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863679 | TATACACACATATAT[A/G]TATATACACACACAT | 83860 |
rs11255416 | snp | G/T | 0.476168 | 0.108512 | intron-variant | TAF3 | GRCh38.p7 | 10:7864006 | AATTCATCCTGCTCC[G/T]TCATCCCCTTATCCT | 83860 |
rs11255417 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865110 | TCATGGGAAGCTTCA[A/G]AGGGAAGTGAGTGGG | 83860 |
rs11255418 | snp | C/G | 0.347253 | 0.230308 | intron-variant | TAF3 | GRCh38.p7 | 10:7871294 | ATTATTGAGATCTGT[C/G]TGCTAAGCATATATT | 83860 |
rs11255419 | snp | A/G | 0.347253 | 0.230308 | intron-variant | TAF3 | GRCh38.p7 | 10:7872542 | AGCAAATTACTCAAT[A/G]GGGAACGTTTAAAAC | 83860 |
rs11255420 | snp | C/T | 0.423726 | 0.179776 | intron-variant | TAF3 | GRCh38.p7 | 10:7873629 | TTCTCCCCCCCCCCC[C/T]GTCAAAAGGGGGTGT | 83860 |
rs11255421 | snp | A/C | 0.338069 | 0.233974 | intron-variant | TAF3 | GRCh38.p7 | 10:7873950 | TACCGCTGTGTTTCC[A/C]CTCGAGAGGCCATTG | 83860 |
rs11255422 | snp | C/T | 0.362941 | 0.223034 | intron-variant | TAF3 | GRCh38.p7 | 10:7875606 | AGAGAAGTTGACTGC[C/T]TCTTTTCAAAAGTTA | 83860 |
rs11255424 | snp | A/G | 0.365646 | 0.221644 | intron-variant | TAF3 | GRCh38.p7 | 10:7886129 | TGGGGGGGTCTCACT[A/G]TGTTGCCTGGGCTGG | 83860 |
rs11255425 | snp | A/G | 0.370365 | 0.219117 | intron-variant | TAF3 | GRCh38.p7 | 10:7887245 | TTTAAAAAAAAAAAA[A/G]AAAGAAAGAAAGCTG | 83860 |
rs11255426 | snp | A/T | 0.491936 | 0.0629843 | intron-variant | TAF3 | GRCh38.p7 | 10:7891318 | GAATGATTAAGGTGT[A/T]CATAGTAAAAGACAC | 83860 |
rs11255427 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7892187 | TTCTGGAAGAGTTTC[A/C]AATTTTCTATGCTCT | 83860 |
rs11255428 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7895794 | GTATCTGTTTCTTAG[C/G]GGTGAAGTGAAGATA | 83860 |
rs11255429 | snp | G/T | 0.341685 | 0.232581 | intron-variant | TAF3 | GRCh38.p7 | 10:7897931 | CTCCCAAAGTGCTGG[G/T]ATTATGGGCATGAGC | 83860 |
rs11255430 | snp | C/T | 0.438946 | 0.163706 | intron-variant | TAF3 | GRCh38.p7 | 10:7898375 | AACATGGTGAAACCC[C/T]GTCTCTACAAAAATA | 83860 |
rs11255431 | snp | A/G | 0.159622 | 0.233092 | intron-variant | TAF3 | GRCh38.p7 | 10:7900018 | GTCCACTCATATCCA[A/G]CTCCCTTCTTATTTG | 83860 |
rs11255432 | snp | C/T | 0.361894 | 0.223562 | intron-variant | TAF3 | GRCh38.p7 | 10:7902392 | TGCACCACTGCACTC[C/T]AGCCTGGGCAACAAG | 83860 |
rs11255433 | snp | C/T | 0.400504 | 0.199621 | intron-variant | TAF3 | GRCh38.p7 | 10:7904284 | GCCCTGAAATGTTGC[C/T]TCTCTGATGAGCCCT | 83860 |
rs11255434 | snp | G/T | 0.325799 | 0.238232 | intron-variant | TAF3 | GRCh38.p7 | 10:7905407 | TTTTAGACAAAACCT[G/T]TGTTTTCATACACGA | 83860 |
rs11255435 | snp | A/G | 0.327211 | 0.237778 | intron-variant | TAF3 | GRCh38.p7 | 10:7908384 | AAATTGGAAAGTCAT[A/G]TAATTAATCAAAATC | 83860 |
rs11255436 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7910572 | TTTTAGTAGAGGCAG[A/G]GTTTCACCATGTTGG | 83860 |
rs11255437 | snp | A/G | 0.121717 | 0.214577 | intron-variant | TAF3 | GRCh38.p7 | 10:7911665 | TCATCCTGAACGTAC[A/G]CTTAGTTTGTCTCAT | 83860 |
rs11255438 | snp | C/T | 0.118584 | 0.212673 | intron-variant | TAF3 | GRCh38.p7 | 10:7913159 | GTCAGATCAGGGCCC[C/T]ACTATTCTGACCTCA | 83860 |
rs11255439 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7913382 | GCCACTCCAGCTCTC[A/C]TTCGCCCAGGCTTGA | 83860 |
rs11255440 | snp | G/T | 0.356383 | 0.226236 | intron-variant | TAF3 | GRCh38.p7 | 10:7914267 | ATGTCCGAGATTTGT[G/T]TTAAACGATGTCGGG | 83860 |
rs11255441 | snp | C/T | 0.493386 | 0.0571263 | intron-variant | TAF3 | GRCh38.p7 | 10:7915450 | gagatcgagaccatc[C/T]tggctaacacggtga | 83860 |
rs11255442 | snp | C/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7918821 | TCAAAAAAGGAAGAG[C/G]CATAACCCTTTCATT | 83860 |
rs11255443 | snp | A/G | 0.141934 | 0.225437 | intron-variant | TAF3 | GRCh38.p7 | 10:7920562 | GAAAATAATCTTCTG[A/G]TATCTATTCTGTATT | 83860 |
rs11255444 | snp | C/G | 0.365646 | 0.221644 | intron-variant | TAF3 | GRCh38.p7 | 10:7921701 | GAATATTTCAGGTAA[C/G]GTTGTATAGTCTTTT | 83860 |
rs11255445 | snp | A/G | 0.123105 | 0.215401 | intron-variant | TAF3 | GRCh38.p7 | 10:7926856 | TAAATTTACTTTATC[A/G]TAACAACTTTTTGTA | 83860 |
rs11255446 | snp | A/G | 0.498632 | 0.0261223 | intron-variant | TAF3 | GRCh38.p7 | 10:7927883 | GAAGTTGCAGAAATA[A/G]CGGGCTATGTTTAAA | 83860 |
rs11255447 | snp | A/C | 0.49621 | 0.0433651 | intron-variant | TAF3 | GRCh38.p7 | 10:7927888 | TGCAGAAATAACGGG[A/C]TATGTTTAAAAGTGT | 83860 |
rs11255449 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7933110 | AAACAAAAAAAAAAA[A/T]ACCTGGCTACTTTGA | 83860 |
rs11255450 | snp | C/G | 0.448195 | 0.152377 | intron-variant | TAF3 | GRCh38.p7 | 10:7936768 | AACGTATAAAGACAT[C/G]TATCTACCATTGCAG | 83860 |
rs11255451 | snp | G/T | 0.441432 | 0.160792 | intron-variant | TAF3 | GRCh38.p7 | 10:7937278 | GTCTTCCTAATTGGC[G/T]GTATCATTTTGCATT | 83860 |
rs11255453 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7938350 | TCTTGATGGTTATCA[A/G]GCTGTTATATTTTAG | 83860 |
rs11255454 | snp | A/G | 0.438806 | 0.163867 | intron-variant | TAF3 | GRCh38.p7 | 10:7948354 | TCAGCCTCTTAAAGT[A/G]TTGGGATTACAGGCA | 83860 |
rs11255455 | snp | A/C | 0.438806 | 0.163867 | intron-variant | TAF3 | GRCh38.p7 | 10:7949489 | CCTTTCCCTTTGCAT[A/C]GCATTATGTAAGTCC | 83860 |
rs11255456 | snp | G/T | 0.454061 | 0.144427 | intron-variant | TAF3 | GRCh38.p7 | 10:7950655 | TCCTCATTATGCACA[G/T]ATTCTGTTTCTCACA | 83860 |
rs11255457 | snp | C/T | 0.441705 | 0.160466 | intron-variant | TAF3 | GRCh38.p7 | 10:7950927 | CTGTGATGTGCCTCA[C/T]AGAGAAAATGCATGT | 83860 |
rs11255458 | snp | C/T | 0.31721 | 0.240796 | intron-variant | TAF3 | GRCh38.p7 | 10:7951437 | GCTCTGGGCCACACA[C/T]TTCATCACCCCGCAG | 83860 |
rs11255459 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | TAF3 | GRCh38.p7 | 10:7952109 | ATTTGTGAATGTGTG[G/T]TGTTTGATTATAAAT | 83860 |
rs11255460 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957798 | CTCTCTAGCGCGctc[G/T]ctctctctctctctc | 83860 |
rs11255461 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957800 | CTCTAGCGCGctctc[G/T]ctctctctctctctc | 83860 |
rs11255462 | snp | A/G | 0.367913 | 0.220446 | intron-variant | TAF3 | GRCh38.p7 | 10:7966371 | AGAAAGTAATCCCAC[A/G]TGGCAGAAATGTTTG | 83860 |
rs11255463 | snp | A/C | 0.492918 | 0.0590819 | intron-variant | TAF3 | GRCh38.p7 | 10:7966780 | AACTTACCTAGAAAA[A/C]TGAGTGTATTTGACA | 83860 |
rs11255464 | snp | C/T | 0.135484 | 0.22223 | intron-variant | TAF3 | GRCh38.p7 | 10:7967437 | TAGGGAAGAAAAGTC[C/T]CCCAGACCACCTTGG | 83860 |
rs11255465 | snp | A/C | 0.120674 | 0.21395 | intron-variant | TAF3 | GRCh38.p7 | 10:7967902 | TCTTTGGAATATTAG[A/C]CCTTGATACAAATAG | 83860 |
rs11255466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969261 | gatagcaccactgca[C/G]ttcagcttgggcaac | 83860 |
rs11255467 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7973384 | AATAAGAAATATCAC[G/T]TCTAATACCTCATCA | 83860 |
rs11255468 | snp | A/G | 0.368529 | 0.220116 | intron-variant | TAF3 | GRCh38.p7 | 10:7976083 | GATTATATGATCTGC[A/G]AACCAACAATTGTGA | 83860 |
rs11255470 | snp | A/T | 0.225301 | 0.248777 | intron-variant | TAF3 | GRCh38.p7 | 10:7985696 | GTCTGCCGTTTGGAC[A/T]CTGTCCCCTAAGCCC | 83860 |
rs11255471 | snp | C/T | 0.365853 | 0.221536 | intron-variant | TAF3 | GRCh38.p7 | 10:7985751 | ATTTTTGTGGTACTA[C/T]GCTAGACTCAGTCTC | 83860 |
rs11255473 | snp | A/G | 0.432504 | 0.170857 | intron-variant | TAF3 | GRCh38.p7 | 10:7992382 | GTAGTAGACTTGAAA[A/G]TAGTGAATTTGGATC | 83860 |
rs11255475 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000720 | GGAGGCAGAGGTTGC[A/T]GTGAGCCAAGATTGC | 83860 |
rs11255476 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000729 | GGTTGCAGTGAGCCA[A/T]GATTGCACCAGCACA | 83860 |
rs11255477 | snp | A/G | 0.184521 | 0.241273 | intron-variant | TAF3 | GRCh38.p7 | 10:8007196 | ATACCATGGAATACA[A/G]TATAGTAATTAGAAT | 83860 |
rs11255478 | snp | C/G | 0.247905 | 0.249991 | intron-variant | TAF3 | GRCh38.p7 | 10:8008018 | CAGCTCTAGCGACCT[C/G]CGGCAGCATCACCAG | 83860 |
rs11593082 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | TAF3 | GRCh38.p7 | 10:7998468 | TTGGTCAACAATCTG[C/T]TTCTATCTGTTGGCC | 83860 |
rs11594292 | snp | C/T | 0.439502 | 0.163061 | intron-variant | TAF3 | GRCh38.p7 | 10:7905585 | AGCAATATACTCCTT[C/T]AAAAACTTAAGCAGG | 83860 |
rs11594582 | snp | C/G | 0.312593 | 0.242037 | intron-variant | TAF3 | GRCh38.p7 | 10:7853104 | tttgagagtgagttg[C/G]caaatgttgtttaat | 83860 |
rs11594671 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7860808 | tttctttctttcttt[C/T]tttttttttgaaata | 83860 |
rs11594885 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983725 | gcacctatactccca[A/G]ctacttgggaggctg | 83860 |
rs11598777 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7835007 | TTCATCAGTTTTTTC[A/G]AGTGTGTGTTTCTCT | 83860 |
rs11813449 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | TAF3 | GRCh38.p7 | 10:8007680 | TGGTTCAAAAGCTGC[C/T]ACCCGTTTACTcaaa | 83860 |
rs11813808 | snp | A/G | 0.160609 | 0.233472 | intron-variant | TAF3 | GRCh38.p7 | 10:7980529 | AGATGACTTTCCAAG[A/G]ACCTCAGATTCCTTT | 83860 |
rs11814948 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7882244 | CAAGCATCAATCTTA[A/G]CATGTTAGATTTGGA | 83860 |
rs11817776 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | TAF3 | GRCh38.p7 | 10:7980944 | ACTTACAGTGTTCAT[C/T]CTTTTCCTCATTTCT | 83860 |
rs11818800 | snp | C/T | 0.158962 | 0.232835 | intron-variant | TAF3 | GRCh38.p7 | 10:7982731 | TAAAGGAAGGTGTTT[C/T]ACTTTCTCAGGAGAG | 83860 |
rs12217782 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957802 | CTAGCGCGctctctc[G/T]ctctctctctctctc | 83860 |
rs12217809 | snp | C/T | 0.32627 | 0.238082 | intron-variant | TAF3 | GRCh38.p7 | 10:7887206 | CACTGCACTCCTGCC[C/T]GGGTGACAGAGCCAG | 83860 |
rs12217954 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7980277 | AAATTATACCTTCTA[A/G]TTGGAAGATCTTTAA | 83860 |
rs12218120 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850695 | aaaaaaaatatatat[A/G]tatatatatatacac | 83860 |
rs12218246 | snp | A/C | 0.342806 | 0.232136 | intron-variant | TAF3 | GRCh38.p7 | 10:7908975 | GATGCTGCTATGCTG[A/C]TAAGGGCTGGGAGTC | 83860 |
rs12218503 | snp | C/T | 0.342806 | 0.232136 | intron-variant | TAF3 | GRCh38.p7 | 10:7909217 | CCCATTCTAGGCTTA[C/T]TGGATCAGAGCCTCT | 83860 |
rs12218756 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:8001592 | ATTGTCGTGCAGTCA[A/G]ATCAGCATTTCCCTT | 83860 |
rs12218807 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7975899 | GCAGCTAGTCAGTGA[A/C]TAACAGTAAACCAGT | 83860 |
rs12219274 | snp | A/G | 0.134119 | 0.221521 | intron-variant | TAF3 | GRCh38.p7 | 10:7899628 | GAAGCTTCCATTCCC[A/G]TTGATACTGAAGAAC | 83860 |
rs12219305 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829176 | TTAAAAtttaaaata[C/G]actattttttagaac | 83860 |
rs12219454 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7865506 | AAACAAACAAACAAA[C/G]AAACAAACAGAAAGT | 83860 |
rs12219539 | snp | C/T | 0.342806 | 0.232136 | intron-variant | TAF3 | GRCh38.p7 | 10:7908936 | ATGGAGCCCAGAACT[C/T]GCATTTCTAGCAAGT | 83860 |
rs12219547 | snp | C/T | 0.343254 | 0.231956 | intron-variant | TAF3 | GRCh38.p7 | 10:7909034 | TAGCAGGTACAAAGG[C/T]CAGGAGGGAGACATG | 83860 |
rs12219763 | snp | A/G | 0.317692 | 0.240661 | intron-variant | TAF3 | GRCh38.p7 | 10:7931731 | TGGGTAGTCAATCAG[A/G]CAACAAGTATTAATA | 83860 |
rs12220069 | snp | A/G | 0.170084 | 0.236883 | intron-variant | TAF3 | GRCh38.p7 | 10:7837708 | agaggctgaggtggt[A/G]taagtactcagaggc | 83860 |
rs12220205 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7845964 | GTGTGtttttgtttt[G/T]tttttttttttttga | 83860 |
rs12220363 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7909024 | GCTGGTGGCTTAGCA[A/G]GTACAAAGGTCAGGA | 83860 |
rs12240458 | snp | G/T | 0.19459 | 0.243782 | intron-variant | TAF3 | GRCh38.p7 | 10:8012394 | GAGGTTGTTTTACAG[G/T]GATTAAATGAAATGA | 83860 |
rs12243636 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7873382 | AGCAGGTAATTTAAT[A/G]TTTACTTAGTGATTT | 83860 |
rs12244839 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7882627 | TCAACATAAGGAAGA[A/G]TTCTCCAACAGTCAG | 83860 |
rs12244989 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7998263 | TATATATATATATAT[A/G]TGTATATATATATAT | 83860 |
rs12245532 | snp | C/T | 0.246769 | 0.249979 | intron-variant | TAF3 | GRCh38.p7 | 10:8007874 | TGAGTAATCCAAGGC[C/T]ACAGGTCTAGTCTCT | 83860 |
rs12246740 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920328 | tgtgtgtgtgtgtgt[A/G]tgtatgtgtgtgtgt | 83860 |
rs12249718 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7997458 | TGTGCAGCTGGGGAG[A/G]TGAGGACGGGCTCTT | 83860 |
rs12253103 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:8007747 | caaaatggggtaatc[A/G]ttacttctttgatgt | 83860 |
rs12253631 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:8002669 | attccgcactgattg[A/C]agacagatttttttt | 83860 |
rs12257496 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7830851 | ACAGTTTATTTGTTA[A/G]AAATCTGGGTTGTTT | 83860 |
rs12257571 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831027 | cttttgttggtgtta[A/G]cagtgctgatgctca | 83860 |
rs12258684 | snp | A/G | 0.296619 | 0.245615 | intron-variant | TAF3 | GRCh38.p7 | 10:7991700 | ACATGCTCTAAATAA[A/G]TATATATACACTATA | 83860 |
rs12259679 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7919153 | TAGGGGCCAGAAAAC[C/T]GTGTAGGAATTAGAA | 83860 |
rs12260718 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7849927 | ctcgggcagtctact[C/T]accttggcctcccaa | 83860 |
rs12260852 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7902592 | gttacatcaggaggc[G/T]tataatgtcaggctc | 83860 |
rs12263118 | snp | A/G/T | 0.0682572 | 0.171956 | intron-variant | TAF3 | GRCh38.p7 | 10:7971242 | AGAGTTTACTTAGAC[A/G/T]GTGTTTCTAAATGGA | 83860 |
rs12263465 | snp | A/G | 2.98521e-05 | 0.00386331 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009195 | gctcgtcagccctgc[A/G]cccgtgccgctgccg | 83860 |
rs12263680 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7926988 | AAAGATGAAAGTGGC[C/T]TACCATGGAAAATAC | 83860 |
rs12264202 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7848009 | tcctgacctcaggtg[A/G]tccacccatcttggc | 83860 |
rs12265481 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972693 | TTAATTTTTACATAT[G/T]GTATTATTTAGGGTT | 83860 |
rs12267616 | snp | A/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7913569 | ACTCACCACCCAATC[A/T]GGCAAACCTATCTGT | 83860 |
rs12268560 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7971718 | TTAAATCTCTTGAGC[A/G]ATTTTCATTTTTTGC | 83860 |
rs12269561 | snp | A/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7920481 | CAATTTAAATGATAA[A/T]AACATTTCTGGCCAT | 83860 |
rs12358644 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974988 | ctgaggcaggagaat[C/T]tcttgaacctgggag | 83860 |
rs12411531 | snp | C/T | 0.139564 | 0.224285 | intron-variant | TAF3 | GRCh38.p7 | 10:7896073 | GTGGGTTACCAATGA[C/T]AGTTGAAGTAACTGC | 83860 |
rs12412852 | snp | A/G | 0.120674 | 0.21395 | intron-variant | TAF3 | GRCh38.p7 | 10:7957122 | AACTTTAGCACAAGC[A/G]GAAAAGGTGACATCA | 83860 |
rs12412991 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7863692 | atatatatacacaca[C/T]atatatatatataca | 83860 |
rs12414427 | snp | A/C | 0.112631 | 0.208878 | intron-variant | TAF3 | GRCh38.p7 | 10:7842970 | TGCAATAATATCCTC[A/C]GGAATTCTTTCTAAT | 83860 |
rs12414660 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863716 | atatacacatatata[C/T]atacacatatatata | 83860 |
rs12414661 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7863718 | atacacatatatata[C/T]acacatatatatata | 83860 |
rs12414886 | snp | A/T | 0.439224 | 0.163383 | intron-variant | TAF3 | GRCh38.p7 | 10:7910328 | TGCTACAACATACAA[A/T]CATCTAAATATCAGG | 83860 |
rs12415744 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7856784 | agattagggttttat[C/T]taaaggactccgaag | 83860 |
rs12415786 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842350 | ttttttgtagagatg[A/G]ggtttcagtatattg | 83860 |
rs12569610 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7872364 | TTATTCTTTGTGGCA[A/G]AGTTTGTGGATGGCG | 83860 |
rs12569614 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7872418 | GTATAGCCAATGCCA[A/G]AACTGTTGCCTATTA | 83860 |
rs12569620 | snp | A/G | 0.342134 | 0.232404 | intron-variant | TAF3 | GRCh38.p7 | 10:7896545 | CAGCGTGCATGCCAC[A/G]TTCTGTAACCTCTCA | 83860 |
rs12570395 | snp | A/G | 0.35809 | 0.225425 | intron-variant | TAF3 | GRCh38.p7 | 10:7853652 | aactagaggtcagca[A/G]actgcctggcctgca | 83860 |
rs12570800 | snp | A/G | 0.357238 | 0.225832 | intron-variant | TAF3 | GRCh38.p7 | 10:7851937 | ggcgtgagccaccat[A/G]cctggcttttttttt | 83860 |
rs12572952 | snp | C/T | 0.32627 | 0.238082 | intron-variant | TAF3 | GRCh38.p7 | 10:7896544 | ACAGCGTGCATGCCA[C/T]ATTCTGTAACCTCTC | 83860 |
rs12573264 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7945372 | CATTTTTTCCCATTA[G/T]TGGATTAAAAAAACT | 83860 |
rs12761785 | snp | A/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7923351 | TGTTTTATATGTCTG[A/T]TTATTACCTTTTGTT | 83860 |
rs12762606 | snp | C/T | 0.375 | 0.216506 | intron-variant | TAF3 | GRCh38.p7 | 10:7858825 | GTGTGTGTGTGTGTG[C/T]GTGCGCGCGCCTGCA | 83860 |
rs12763699 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971278 | TGTAAAGACCTTAAT[G/T]GCTGAGAAATACAAG | 83860 |
rs12763709 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971288 | TTAATTGCTGAGAAA[A/T]ACAAGATGGTTACAG | 83860 |
rs12763730 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971323 | AGTTCAGCATCCAAA[G/T]GTTAGGTTATTCTGT | 83860 |
rs12763771 | snp | A/C | 0.107694 | 0.205546 | intron-variant | TAF3 | GRCh38.p7 | 10:7947397 | gtagttccttccagc[A/C]tgaagcttattgcat | 83860 |
rs12766093 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871436 | ACAAATAACTGCTGC[C/T]ttttttttttttttt | 83860 |
rs12766242 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7825710 | aggcagaataatata[A/T]gtacattccacattt | 83860 |
rs12767920 | snp | C/T | 0.106633 | 0.204807 | intron-variant | TAF3 | GRCh38.p7 | 10:8009996 | ggctcactgcagccc[C/T]tgcctcccaggctca | 83860 |
rs12768403 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830504 | tttttttttttttga[A/G]aaggagtcttgctct | 83860 |
rs12768854 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7993147 | TGTAATCTAGACCTG[G/T]TATTTTTAATCCACA | 83860 |
rs12774096 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7836236 | GTCCCTCTACATCCA[C/T]CTCTCAGACCCTGCA | 83860 |
rs12774248 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7836959 | TTggttgagtgtgat[A/G]gctcatgcctataat | 83860 |
rs12775599 | snp | G/T | 0.00486615 | 0.0490856 | intron-variant | TAF3 | GRCh38.p7 | 10:7860494 | ATTATTTTATGAGTG[G/T]ATTTGTACATTTTAt | 83860 |
rs12775800 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7860549 | tcatgtactacttgg[G/T]tgtccagaggtgtag | 83860 |
rs12775810 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830472 | TTTTCACTTTACATG[G/T]Ctttttttttttttt | 83860 |
rs12775812 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7860565 | tgtccagaggtgtag[C/T]tcatatagaaaaaaa | 83860 |
rs12777430 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7839676 | TTCCTTTCAAATTGG[G/T]TTCTTGAGTACAATT | 83860 |
rs12777575 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7957685 | AGTCCTTTTCTCCCG[G/T]TTCAGAACACTAAAA | 83860 |
rs12778232 | snp | C/T | 0.107694 | 0.205546 | intron-variant | TAF3 | GRCh38.p7 | 10:7988126 | AATTTTTAAAAACAG[C/T]TTTTAAGGCCAATAT | 83860 |
rs12778847 | snp | A/G | 0.107341 | 0.205301 | intron-variant | TAF3 | GRCh38.p7 | 10:8007808 | taaagtgcctagtat[A/G]acctctaacttctta | 83860 |
rs12780500 | snp | A/C | 0.388398 | 0.208197 | intron-variant | TAF3 | GRCh38.p7 | 10:7983399 | TTTTGCATTTTTATA[A/C]AAGTGTCCTGGGGAG | 83860 |
rs12780620 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971279 | GTAAAGACCTTAATT[A/G]CTGAGAAATACAAGA | 83860 |
rs12782002 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971241 | CAGAGTTTACTTAGA[C/T]TGTGTTTCTAAATGG | 83860 |
rs12782204 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7846203 | acctcgtgatctgcc[C/T]gccttggcctcccga | 83860 |
rs12782467 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829057 | aaaaaaaaaaaaaaa[A/G/T]GGAATATAAACCATG | 83860 |
rs12782612 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971240 | TCAGAGTTTACTTAG[A/C]CTGTGTTTCTAAATG | 83860 |
rs12782810 | snp | A/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971270 | GGAAATAATGTAAAG[A/T]CCTTAATTGCTGAGA | 83860 |
rs12782819 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971286 | CCTTAATTGCTGAGA[A/C]ATACAAGATGGTTAC | 83860 |
rs12782845 | snp | A/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7971321 | ATAGTTCAGCATCCA[A/T]ATGTTAGGTTATTCT | 83860 |
rs12783565 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7999323 | ATGTGGATGAGAGAG[A/C]CAGATCTGCACACAA | 83860 |
rs12783635 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007544 | CTGTCTGTTATATTG[G/T]TTTCTCTGTGTGTGA | 83860 |
rs12783641 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007553 | ATATTGTTTTCTCTG[G/T]GTGTGAAATtatata | 83860 |
rs12784360 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7855311 | agcagctgcctctac[A/C]aaagactgacttcaa | 83860 |
rs17143029 | snp | A/G | 0.401392 | 0.198948 | intron-variant | TAF3 | GRCh38.p7 | 10:7839520 | AAGTCACATGGCTGC[A/G]AAGTGATAGAGGTGA | 83860 |
rs17143033 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7849383 | TAAAGGTTCAGTGAT[C/G]CATAAGGAATATTTG | 83860 |
rs17143036 | snp | A/G | 0.00356505 | 0.0420692 | intron-variant | TAF3 | GRCh38.p7 | 10:7857337 | TTCCCTATCACAGGT[A/G]CATAGTTTTATCCGA | 83860 |
rs17143038 | snp | C/T | 0.302449 | 0.244436 | intron-variant | TAF3 | GRCh38.p7 | 10:7857894 | TCACACCCCAGGGTT[C/T]TTTTCAACATTTCTG | 83860 |
rs17143046 | snp | C/G | 0.354019 | 0.227333 | intron-variant | TAF3 | GRCh38.p7 | 10:7874802 | AGATTACATGGAAAA[C/G]TTTTTTCATCGATTT | 83860 |
rs17143047 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7874814 | AAACTTTTTTCATCG[A/T]TTTCTTAGCTGTATG | 83860 |
rs17143049 | snp | A/T | 0.346147 | 0.230772 | intron-variant | TAF3 | GRCh38.p7 | 10:7874905 | TTCCTTCTTCAGTAC[A/T]GCCATTTTAAAAAAT | 83860 |
rs17143050 | snp | A/C | 0.338296 | 0.233889 | intron-variant | TAF3 | GRCh38.p7 | 10:7875035 | TCAATTATAGATAGC[A/C]GTTTGTAGGTTTTCC | 83860 |
rs17143053 | snp | C/G | 0.030665 | 0.119967 | intron-variant | TAF3 | GRCh38.p7 | 10:7878667 | GAAATTCCCTCTCTA[C/G]ATGCACTATAATTAA | 83860 |
rs17143057 | snp | C/T | 0.213937 | 0.247385 | intron-variant | TAF3 | GRCh38.p7 | 10:7879248 | TTTGTCATAAAATTA[C/T]TTTCACCAATTATAG | 83860 |
rs17143062 | snp | A/G | 0.326976 | 0.237854 | intron-variant | TAF3 | GRCh38.p7 | 10:7885634 | CATCTATATTCAATT[A/G]TCCATGTTTCTAATT | 83860 |
rs17143071 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7894359 | AGTATTATACAGAAC[A/G]TCAAAATCCATCAAG | 83860 |
rs17143077 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | TAF3 | GRCh38.p7 | 10:7900445 | GACAGCTTTGTACAT[C/G]ACTGCTACTCCTCGG | 83860 |
rs17143085 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7906218 | TAGTTTCAGTGTCTT[A/G]TCTTTAATTTCAGTA | 83860 |
rs17143090 | snp | A/G | 0.327211 | 0.237778 | intron-variant | TAF3 | GRCh38.p7 | 10:7909701 | GGCAGATACTTTCTT[A/G]GGCCCATTTGATTCT | 83860 |
rs17143098 | snp | C/T | 0.35207 | 0.228214 | intron-variant | TAF3 | GRCh38.p7 | 10:7912866 | CCCCGGAATCCCTTA[C/T]GCTGGTTACCTTCAC | 83860 |
rs17143115 | snp | C/T | 0.138546 | 0.223781 | intron-variant | TAF3 | GRCh38.p7 | 10:7922378 | TTTCCATTGTGAATG[C/T]TGTACTGTCTTAATC | 83860 |
rs17143125 | snp | C/T | 0.339203 | 0.233544 | intron-variant | TAF3 | GRCh38.p7 | 10:7941928 | GGAACTCTTTTTGTT[C/T]TTAATAATTATATAT | 83860 |
rs17143136 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7960024 | CTGAGCTATATCCAG[A/G]TTAGTCCCCAGAGTT | 83860 |
rs17143139 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7960382 | CAAACGTTTTTTTGT[A/G]AAGAGCTGGATAGTA | 83860 |
rs17143144 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7962183 | ATTGTGTTTGAGTCC[G/T]TGCTCAAGTCTTATA | 83860 |
rs17143151 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7978622 | CCTATCTTACCTACA[C/G]AAGCATGAAGAATGT | 83860 |
rs17143168 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7995696 | GCATTAAAAGATAAA[A/G]TGTTTGCTACTTGAT | 83860 |
rs17366712 | snp | C/G | 0.0696164 | 0.173095 | missense | TAF3 | GRCh38.p7 | 10:7964556 | CTTCAGCTACACTCA[C/G]TGAAAAAATCAGTAA | 83860 |
rs17444909 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TAF3 | GRCh38.p7 | 10:7960694 | TTCCCTAGCTTAGAG[A/G]GAGCACCTTGTCAGT | 83860 |
rs17445476 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7991118 | TAATTTCAGTCGTCT[C/T]GTCTTGCCTCAGAGA | 83860 |
rs28363949 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882299 | TCCTCATTTACAACA[G/T]GTTTGTGCAAGACAT | 83860 |
rs28453954 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839612 | CATTATTCTCAAGGG[C/G]ACAGATAGAAGAACA | 83860 |
rs28517338 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839613 | ATTATTCTCAAGGGC[A/C]CAGATAGAAGAACAA | 83860 |
rs28667786 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | TAF3 | GRCh38.p7 | 10:7976346 | CCACCTCCTGAGTTC[A/G]AGCGATTCTCCTGCC | 83860 |
rs28696213 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839655 | GTGGCTCTTCGTTTG[C/T]TTCTTTTCCTTTCAA | 83860 |
rs33964713 | in-del | -/G | 0.488363 | 0.0753851 | intron-variant | TAF3 | GRCh38.p7 | 10:7946718 | ACAGAGTAAGACCCT[-/G]GGTCTCAAACGAAAA | 83860 |
rs33967138 | in-del | -/T | 0.418007 | 0.185132 | intron-variant | TAF3 | GRCh38.p7 | 10:7895727 | TAATTGTGTGGCCTC[-/T]TATCTACAGTTATAG | 83860 |
rs34069819 | in-del | -/AATA | 0.375 | 0.216506 | intron-variant | TAF3 | GRCh38.p7 | 10:7935297 | ATAAATAAATAAATA[-/AATA]GAAGAAAAATAAAGC | 83860 |
rs34114853 | in-del | -/T | 0.394721 | 0.203852 | intron-variant | TAF3 | GRCh38.p7 | 10:7850055 | TCATTGAGTGAGAAG[-/T]TTACAGGCTTTGCTT | 83860 |
rs34130137 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006840 | ACATGGCACGGGGCC[-/C]GGCAGTTCCCATCTG | 83860 |
rs34132762 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870628 | CTTGTTAAACTTCTA[-/A]CAGACTCCTGACTTG | 83860 |
rs34133343 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7949759 | TTCTTCTATAAAACA[-/T]TTTTTTTAACTGCAT | 83860 |
rs34163537 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845960 | GTTTGTGTGTTTTTG[-/T]TTTTTTTTTTTTTTT | 83860 |
rs34173989 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923704 | AAAAGAGTACCTCCC[-/C]TGCTTTTAAACACAA | 83860 |
rs34180336 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843647 | TCTTTTTTTTTTTTT[-/T]GAGCACTGTGATCAG | 83860 |
rs34251155 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950574 | AAAATCTTTTCTTTT[-/T]AAGTCAGTAGTCCGT | 83860 |
rs34253534 | in-del | -/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7836294 | TTTCTTTTTTCTTTC[-/T]TTTTTTTTTTTTTGA | 83860 |
rs34274060 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014005 | CAATTAACTGCAAAA[-/A]CCCAAGAGTCCTTAG | 83860 |
rs34293337 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954788 | TGAGATTCAGAGTGC[A/C]CTCCATAGGCGAATG | 83860 |
rs34307551 | in-del | -/GA | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7841651 | GTCACCCAAGGGACA[-/GA]TGATAGGAAGGACCA | 83860 |
rs34375948 | in-del | -/GTTCAAAGTT | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817411 | AAATGTGAATATCAT[-/GTTCAAAGTT]CTGGAATAGTCCCTG | 83860 |
rs34385673 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924233 | CCAAAACTTCTTTTT[-/T]GGTAGAGTACACCGA | 83860 |
rs34392128 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876167 | GCGGTGTTTTATATT[-/G]TTTCTTTTCTTTGTT | 83860 |
rs34397533 | in-del | -/A | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7822489 | TATAGAAAAAAAAAA[-/A]TCAAAGACTGCAGAA | 83860 |
rs34414112 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875559 | GCGGGCACGAAGGGG[-/G]TTGTTGGCCTCCAGT | 83860 |
rs34414978 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833267 | CTATTTTGAGTTTTT[-/T]GGAGGAAACTCCACA | 83860 |
rs34416014 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967777 | AATCAAACTATAAAA[-/A]TGTAGGAACCTGGAG | 83860 |
rs34416999 | in-del | -/A | 0.35894 | 0.225016 | intron-variant | TAF3 | GRCh38.p7 | 10:7845241 | AATGTGGGAACTACC[-/A]AAAAAAAAAAAATCT | 83860 |
rs34431935 | in-del | -/G | 0.411022 | 0.191238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858836 | GTGTGTGCGCGCGCC[-/G]TGCATGTCACTGAAT | 83860 |
rs34439319 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919833 | CATACGGAGGGCTGA[-/A]CTGTGTATGCTTAAT | 83860 |
rs34502665 | snp | A/T | 0.107694 | 0.205546 | intron-variant | TAF3 | GRCh38.p7 | 10:7970729 | TCAGAACAATTAAAA[A/T]TTTTAATGTTTCTTT | 83860 |
rs34510485 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880111 | GCCTTGGTGGCACGC[-/C]ACCTGTAATCTCAGC | 83860 |
rs34532905 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882560 | CATTGTAACCACAGG[-/C]AAAAGACACGTAGGT | 83860 |
rs34538206 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858814 | ATAGGCTCTGTGTGT[-/GT]GTGTGTGTGTGTGCG | 83860 |
rs34558498 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934164 | AAAGGAAAGAACTTT[-/T]AGGACTACCTTAACC | 83860 |
rs34588121 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835327 | CCCATGGGCTGTGGG[-/G]TTGACAAGCTTGCTT | 83860 |
rs34613957 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983445 | AGTTGGTGTACAAAA[-/A]GGATACTTTAGATGT | 83860 |
rs34624118 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999240 | TATTTCTTGAGCTGC[-/G]TGTGTTTAATACTGC | 83860 |
rs34632930 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820073 | ATCTGCGACCACGCT[-/T]GAGCTACCTGCCTTT | 83860 |
rs34643454 | multinucleotide-polymorphism | CA/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896544 | ACAGCGTGCATGCCA[CA/TG]TTCTGTAACCTCTCA | 83860 |
rs34648088 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890406 | TGTAGTCTACGTTCC[-/C]ATCATAGTAGAGTAG | 83860 |
rs34648208 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927938 | GGTCAAGATTTTCTT[-/T]CTCAAAATCTGGACA | 83860 |
rs34660241 | in-del | -/A | 0.478188 | 0.10213 | intron-variant | TAF3 | GRCh38.p7 | 10:7933099 | TAAGATAAAGCAAAC[-/A]AAAAAAAAAATACCT | 83860 |
rs34669002 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994826 | AAAAAAAAAAAAAAA[-/A]TAGCTGGGTGTGGTG | 83860 |
rs34690836 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830806 | TTACCTTTTAGTTTG[G/T]GACTCTCCTTCCATT | 83860 |
rs34693637 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904496 | AGTGCCTGATACACG[-/A]CATTTATCTCATATT | 83860 |
rs34704750 | snp | C/T | 0.108755 | 0.206276 | intron-variant | TAF3 | GRCh38.p7 | 10:7969355 | TCACAGCCATAATAG[C/T]TGTAGCAGTGATAAA | 83860 |
rs34710271 | in-del | -/AGA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888514 | GAGATCTTCTAAAGA[-/AGA]TGTGGAGGTCTGCAG | 83860 |
rs34762128 | in-del | -/A | 0.180702 | 0.240204 | intron-variant | TAF3 | GRCh38.p7 | 10:7904495 | TAGTGCCTGATACAC[-/A]GCATTTATCTCATAT | 83860 |
rs34772258 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953393 | CCTTTAGATCATCCC[-/C]ACACATGGCCAACTA | 83860 |
rs34794475 | in-del | -/T/TT | 0.440057 | 0.162414 | intron-variant | TAF3 | GRCh38.p7 | 10:7877028 | ACTTTTTTTTTTTTT[-/T/TT]CCTAATGGAGATTCC | 83860 |
rs34833399 | in-del | -/TATA | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8007571 | ATATATATATATATA[-/TATA]CCTTTTTTTTTTAAT | 83860 |
rs34852266 | in-del | -/TGAA | 0.111928 | 0.208413 | intron-variant | TAF3 | GRCh38.p7 | 10:7858847 | GCGCCTGCATGTCAC[-/TGAA]TGTACGTGTGAGTGT | 83860 |
rs34866346 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7996858 | TTTTTTTTTTTTTTT[-/T]GTATTTTTGTATTTT | 83860 |
rs34871611 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835701 | TCTTCTCGGGTTGGC[-/C]TGCCGGGCTTTCCAG | 83860 |
rs34874654 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955812 | TCATTATTCCTCAGG[-/C]AGAATGTAGGGAGTG | 83860 |
rs34895330 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832884 | TGCTACAGATATTCC[-/C]AGTTATACTCTTTTA | 83860 |
rs34907761 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7932694 | TTTTTTTTTTTTTTT[-/T]GGAGAGAGGGTCTTG | 83860 |
rs34945620 | in-del | -/TT | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7872233 | TTTTTTTTTTTTTTT[-/TT]CTTTCTTTCCCAGTA | 83860 |
rs34945689 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835819 | ACTCGGGTCTCATGG[-/G]CGCTTGGTGGCATGT | 83860 |
rs35001490 | snp | A/C | | | missense | TAF3 | GRCh38.p7 | 10:7965621 | AAGAAAAGAAAAAGG[A/C]CAAAAAGGAGAAGAA | 83860 |
rs35017664 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973708 | GCTTGTAAATGTTTG[G/T]TTATTTTTGTTATAT | 83860 |
rs35019527 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892609 | TCAAATTATAAAATG[-/G]AAAATATTTATTATC | 83860 |
rs35026998 | in-del | -/ACAA/CAA | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7846621 | GAGGCTAACAAAAAA[-/ACAA/CAA]GGAGAAAAATGATCA | 83860 |
rs35085945 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7837801 | TCCAGCCTGGGTGAC[A/C]GAGTGGGACCCTGTC | 83860 |
rs35093712 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921258 | TTATTTGGTAGTTTT[-/T]CTATCCTTTCCACTT | 83860 |
rs35126084 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7934437 | TCTTTTATCTTACTG[G/T]TATTTATTTATTTAT | 83860 |
rs35129123 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871005 | GATAGAAATTATTTT[-/T]GTATAAGGAAAGACA | 83860 |
rs35135595 | snp | A/C | 0.107341 | 0.205301 | intron-variant | TAF3 | GRCh38.p7 | 10:8004979 | TTATTTTGTCCTAAT[A/C]CTCAGTTTATAGTTC | 83860 |
rs35136024 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | TAF3 | GRCh38.p7 | 10:7966104 | TATATTTTGCACCCA[C/T]ATATTGAGAAAGGCA | 83860 |
rs35143830 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865427 | AGCTTGCAGTGAGCC[-/C]GAGATCGCGCCTCTG | 83860 |
rs35145621 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959327 | AAAAAAAATCTATTT[-/T]AAAACGTTTGTATTT | 83860 |
rs35181779 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7825851 | CAGGTGTTTTTTTTT[-/T]GGGTCTGTACCTTGA | 83860 |
rs35202815 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996186 | GTGGTTCTGGCTCAG[-/G]TCTGTCTGCAAGCTG | 83860 |
rs35210778 | in-del | -/T/TT | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7857926 | TTTTTTTTTTTTTTT[-/T/TT]CTGCTAACCTTAGGG | 83860 |
rs35219363 | in-del | -/TG | 0.38821 | 0.208322 | intron-variant | TAF3 | GRCh38.p7 | 10:7944094 | TAAAATGTTCATGCT[-/TG]TGTGTGTGTGTGTGT | 83860 |
rs35222561 | snp | A/C | 0.275732 | 0.248672 | intron-variant | TAF3 | GRCh38.p7 | 10:8001493 | GTTTATATAAGAAGG[A/C]GTAATGCTTTATTGT | 83860 |
rs35232990 | in-del | -/TGTTCAAAGT | 0.499713 | 0.0119774 | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817410 | AAAATGTGAATATCA[-/TGTTCAAAGT]TCTGGAATAGTCCCT | 83860 |
rs35240361 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817857 | CTTACCTGTTTTTTT[A/T]AAAAAAAAAAAAAAA | 83860 |
rs35264183 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872867 | TAAAATAACATTAAA[-/A]TGTGCATTCATTGCC | 83860 |
rs35268313 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820141 | CTGTTTCTTACCTAG[A/C]GTGTCCTTTGCCCGT | 83860 |
rs35290099 | in-del | -/G | 0.492087 | 0.0623997 | intron-variant | TAF3 | GRCh38.p7 | 10:7835329 | CATGGGCTGTGGGTT[-/G]GACAAGCTTGCTTTA | 83860 |
rs35309786 | in-del | -/TT | 0.157972 | 0.232445 | intron-variant | TAF3 | GRCh38.p7 | 10:7832378 | GACAAAATTTCCTTC[-/TT]TTTTTAAAGGCTGAA | 83860 |
rs35335411 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842134 | GTTTGTCATTGTAGG[-/C]ATATTGAATTAATAT | 83860 |
rs35337660 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000936 | CATCTTACACCTCCC[-/C]TTTTTCTTGGATAGA | 83860 |
rs35345431 | in-del | -/TT | 0.496245 | 0.0431677 | intron-variant | TAF3 | GRCh38.p7 | 10:7927974 | TTTTTGCTCCCCCAC[-/TT]TTTTTTTTGGAGTTC | 83860 |
rs35372003 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946439 | TATTTAAGAAGGTGG[-/G]TGGGCCAGGCACCAT | 83860 |
rs35379190 | in-del | -/A | 0.375 | 0.216506 | intron-variant | TAF3 | GRCh38.p7 | 10:7840538 | TGAAAAAAAAAAAAA[-/A]GATTGGTTTTTTTTC | 83860 |
rs35384946 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930591 | TTCTATATAGTAGCT[-/T]GGCAGTCAAATTTAT | 83860 |
rs35386526 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921793 | TGAATATTGTAGAAG[-/C]AAAATTTGGAAGACT | 83860 |
rs35391531 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843289 | ACTTTTTTTTTTTTT[-/T]GTAGAGATGGGCTCT | 83860 |
rs35403604 | in-del | -/G | 0.356383 | 0.226236 | intron-variant | TAF3 | GRCh38.p7 | 10:7996773 | CAACCTCCACCTCCT[-/G]GGCTCAAGCTATCCT | 83860 |
rs35428970 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851644 | CTTTCCCTTCTCCCC[-/C]TTTCATGTTGGCTTG | 83860 |
rs35459666 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895636 | AGGTTGAGTCTTGGG[-/G]AAATTGGGGCATGAT | 83860 |
rs35472379 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902181 | CAATCCCAGCACTTT[-/T]GGGAGGCTGAGGCAG | 83860 |
rs35491167 | in-del | -/G | 0.450357 | 0.149522 | intron-variant | TAF3 | GRCh38.p7 | 10:7957979 | TGACCAAATTTTGCA[-/G]TTTTATAATACACAG | 83860 |
rs35494554 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959912 | GTCCTGGGTATCCCC[-/C]TGTAGTCCCTTTCTA | 83860 |
rs35528740 | in-del | -/AA | 0.299158 | 0.245119 | intron-variant | TAF3 | GRCh38.p7 | 10:7845661 | ATCAGATTTAGAGTG[-/AA]GGTGAGAGGTCTCAT | 83860 |
rs35541158 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994619 | TCCCAAAGTGCTGGG[-/G]ATTACAGACTGAACC | 83860 |
rs35565870 | in-del | -/T | 0.497881 | 0.0324789 | intron-variant | TAF3 | GRCh38.p7 | 10:7929259 | TGTTGTTTTTTTTTT[-/T]GGTAATAGTCTTCTA | 83860 |
rs35603375 | in-del | -/G | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817603 | TGGGATCAGTTTGGC[-/G]TTTTGAGATGTGTTC | 83860 |
rs35604602 | in-del | -/T | 0.441158 | 0.161117 | intron-variant | TAF3 | GRCh38.p7 | 10:7967237 | TTAGTCATTTATCCC[-/T]TGTGTACCTAGTAAG | 83860 |
rs35610744 | in-del | -/AC | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7881491 | CACACATACACACAA[-/AC]ACACACACACACACA | 83860 |
rs35613020 | in-del | -/C | | | frameshift-variant | TAF3 | GRCh38.p7 | 10:7965235 | GAAACAAAGTATCCC[-/C]TGGAAGGAATTTCTT | 83860 |
rs35634153 | snp | C/T | 0.19334 | 0.243495 | intron-variant | TAF3 | GRCh38.p7 | 10:8009915 | ATGAGCCACCGTGCC[C/T]GGCTTTTTTTTTTTG | 83860 |
rs35690286 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991220 | TACATACACATCCGT[-/G]ATGCATGTATATATA | 83860 |
rs35690942 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | TAF3 | GRCh38.p7 | 10:7844375 | TTTCTTCTTCTTCTT[C/G]TTCTTTTTTTTTTTT | 83860 |
rs35695686 | snp | C/T | 0.194278 | 0.243711 | intron-variant | TAF3 | GRCh38.p7 | 10:8009909 | ACAGGCATGAGCCAC[C/T]GTGCCCGGCTTTTTT | 83860 |
rs35696659 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942677 | CACAGATCCCAAGAA[-/A]GCGCTGGGGAATGTG | 83860 |
rs35725342 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7847776 | AAAACTTCTTTTTTT[A/C]TTAATTTTGAGACAA | 83860 |
rs35755700 | in-del | -/A | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7975092 | AAAAAAAAAAAAAAA[-/A]GAGTGAGATGAAAAT | 83860 |
rs35771089 | in-del | -/A | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817878 | AAAAAAAAAAAAAAA[-/A]AGTTTTATTGGAACC | 83860 |
rs35822603 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | TAF3 | GRCh38.p7 | 10:7867272 | ACACACACACACACA[A/C]AAAACAAAAAACAAA | 83860 |
rs35832187 | multinucleotide-polymorphism | CA/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936996 | CATTTCAGATTCCTC[CA/TG]TATCTTTTTATGGCT | 83860 |
rs35850702 | in-del | -/AAAG | 0.420096 | 0.183214 | intron-variant | TAF3 | GRCh38.p7 | 10:7948005 | GACATACCTTTTATT[-/AAAG]AAAGTTTAAATTGTC | 83860 |
rs35853379 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829650 | ATATCAAAGGTCTAT[-/G]CCTGTCATCATAATT | 83860 |
rs35867978 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847669 | GGTTGGTCTCAAACT[-/T]CCTGGGTTCAAGTGA | 83860 |
rs35873636 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837662 | AAAATAAAAAATAAA[A/C]CAATTAGCCAAGAGT | 83860 |
rs35873776 | in-del | -/T | 0.460813 | 0.134379 | intron-variant | TAF3 | GRCh38.p7 | 10:7864823 | GAAATATAGTTTATC[-/T]TTTTTTTTTTCCTTT | 83860 |
rs35885430 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822457 | TTTATTTTCTTTTTT[-/T]AATGCATCACAGAAG | 83860 |
rs35886980 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890882 | TCTCTTTTTACATTC[-/C]ATATTTCCTTGGTTA | 83860 |
rs35916861 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968946 | TTCGTGGGCAGTCAG[-/T]ACACCTAGTCAGGGT | 83860 |
rs35918792 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822259 | AAAAAAAAAAAAAAA[-/A]GGTGGCCGAAGGGGA | 83860 |
rs35930731 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880285 | ACTCCTTAGACTTTT[-/T]GGGGAAATAACTTTG | 83860 |
rs35934283 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864726 | TCATCTATTTGTTTT[C/T]CAAATATTTCCTCTC | 83860 |
rs35953216 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7862546 | TTATGTTCAGTAAAC[G/T]GTACATGTTTATAAC | 83860 |
rs35985393 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884756 | TTGCTATTACAATGT[-/T]CATTGCTTTTAGTTC | 83860 |
rs36029481 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894574 | TGGTCATTGTTTGAA[-/A]GTTGGAATTCATTTT | 83860 |
rs36048947 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820089 | GAGCTACCTGCCTTT[-/T]CCAAAATGTTTTAAG | 83860 |
rs36055328 | snp | C/T | 0.105924 | 0.204309 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016713 | CCACGTTTAAGTGAG[C/T]AGGTCACGCTACTGA | 83860 |
rs36076376 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946436 | ATTCTATTTAAGAAG[-/G]TGGTGGGCCAGGCAC | 83860 |
rs36091254 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7845977 | TTTTTTTTTTTTTTT[-/T]GAGGCAATGTCTCGC | 83860 |
rs36097611 | snp | C/T | 0.226484 | 0.248892 | intron-variant | TAF3 | GRCh38.p7 | 10:8003220 | TTTCTCTCTCTCTCT[C/T]TTCTTTTATCAGACC | 83860 |
rs36121339 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865813 | GACAAGGACTCTCCC[-/C]GTCACCTCCCCTATC | 83860 |
rs41290305 | snp | A/G | 0.00713715 | 0.0593097 | missense | TAF3 | GRCh38.p7 | 10:7964303 | GCAAAACCATTAGAA[A/G]CAAAGTCATTTACAC | 83860 |
rs41306824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014546 | TCGGGTAAACATGTC[A/G]TAGACTCTAAAAAAT | 83860 |
rs41311222 | snp | A/G | 6.63526e-05 | 0.0057595 | intron-variant | TAF3 | GRCh38.p7 | 10:8013709 | CCCTCCATTTTTGCC[A/G]CTTCCGCTTTGCAAA | 83860 |
rs41368447 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:7957578 | TCAAGGAACTAATGC[A/G]CCAAGAAGATGAACT | 83860 |
rs55656438 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954553 | TTAGTTCTAGTTAAC[A/G]CAGAGCTCTCCATAG | 83860 |
rs55742210 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915788 | GTTTGTGACCAGCCT[C/T]GCCAACATGGTGAAA | 83860 |
rs55781378 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007782 | ATAAGGACTGGATGA[A/G]ATGATGTTTGTAAAG | 83860 |
rs56001648 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850685 | ATCTCAAAAAAAAAA[A/T]AATATATATGTATAT | 83860 |
rs56045608 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988423 | GGTGAAACCCTGTTT[C/T]TACTAAAAATACAGA | 83860 |
rs56056082 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7899035 | TTTTATTCTAGGTGA[A/G]ATTCCCCCAATCTAC | 83860 |
rs56060220 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828972 | GAGGCAGAGGTTGCA[G/T]TCAGCCGAGATCGTG | 83860 |
rs56106381 | snp | A/G | 0.227959 | 0.249026 | intron-variant | TAF3 | GRCh38.p7 | 10:8003451 | ACTTGGAAGATCTTT[A/G]TAAGTCAGTGAACCA | 83860 |
rs56222109 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955026 | AATTAGTCCCAGTTA[A/G]CACAGAGCTCTCCAT | 83860 |
rs56223929 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838849 | TGTTAGGCTGGAGTT[C/T]CAGGGTCTGGGGAAC | 83860 |
rs56262335 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954130 | TAGGTGAATGAATGA[A/G]TTAGTCCCAGTTAAC | 83860 |
rs56304036 | in-del | -/T | 0.464523 | 0.128375 | intron-variant | TAF3 | GRCh38.p7 | 10:7827323 | AAGTAATTTTTTTTT[-/T]GTTAACACATTTATA | 83860 |
rs56363651 | in-del | -/CACACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974165 | ACACACACACACACA[-/CACACACA]AACACACACACGAGA | 83860 |
rs56395044 | in-del | -/A/AAAAAAA | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7988771 | AAAAAAAAAAAAAAA[-/A/AAAAAAA]TCAAGATTATCAAGT | 83860 |
rs56822953 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7820489 | GCTTGATTTCACTGA[C/T]ACTTCTATTACTCTT | 83860 |
rs56955821 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980805 | GGGGCTGGGAGCAGG[-/G]TGAGTGTGACAGCCA | 83860 |
rs57006386 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994735 | TTTGGGAGGCTGAGG[C/T]AGGCAGATCACAAGG | 83860 |
rs57008215 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816501 | TTGGAATTGAATGGA[C/T]TCAGCTGCAGTGTTC | 83860 |
rs57122739 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962941 | CTGATCTTAGAAAAA[C/T]TCAGCCAAGTAGGCA | 83860 |
rs57207229 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856880 | AAAAAAAAAAAAAAA[-/A]GCAGAAAGAATGCTT | 83860 |
rs57236670 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842176 | TTTGTTTTTTTTTTT[-/G]TTTTTTTTTTTTTTT | 83860 |
rs57337865 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | TAF3 | GRCh38.p7 | 10:7958439 | AAATAAGTGAACTAC[A/T]GCTGCCTGCATCAAT | 83860 |
rs57377389 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7851593 | TCACCCAGCTTCACC[C/T]GTATCTACTCATGGC | 83860 |
rs57688972 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990038 | CAGTTAAAATTAACT[-/GT]ATCTATTTTTAAGAG | 83860 |
rs57860144 | in-del | -/GCTCTCTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957794 | CGCTCTCTCTAGCGC[-/GCTCTCTC]TCTCTCTCTCTCTCT | 83860 |
rs58020923 | snp | A/G | 0.17654 | 0.238964 | intron-variant | TAF3 | GRCh38.p7 | 10:7867784 | ATATGGGAGTTGGGG[A/G]CACAGACCCCTGTGC | 83860 |
rs58063040 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7927841 | GCTTATGAAGAGGCA[C/T]TGTTTCCTTTTCTTC | 83860 |
rs58100472 | in-del | -/GCTCTCTCTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957794 | CGCTCTCTCTAGCGC[-/GCTCTCTCTC]TCTCTCTCTCTCTCT | 83860 |
rs58113019 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963000 | AGATTAGGAAACAGG[C/G/T]TCAGAGAGGTTGAGA | 83860 |
rs58136865 | in-del | -/T | 0.0711525 | 0.174681 | intron-variant | TAF3 | GRCh38.p7 | 10:7821222 | ACGTAATTTGGTGAC[-/T]TTTTTTTTAATGCTA | 83860 |
rs58230104 | in-del | -/TGTG/TGTGTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858828 | GTGTGTGTGTGTGTG[-/TGTG/TGTGTG]CGCGCGCCTGCATGT | 83860 |
rs58234860 | in-del | -/CA | 0.317451 | 0.240729 | intron-variant | TAF3 | GRCh38.p7 | 10:7958163 | AGAGGCTAAACAGTT[-/CA]ATAGCCATTACACAT | 83860 |
rs58358249 | in-del | -/TATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998284 | ATATATATATATATA[-/TATA]AATTTAAAAGGGGTA | 83860 |
rs58374830 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929948 | GGCTCACACCTATAA[A/T]TCCAGCACTTTGGGA | 83860 |
rs58492448 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7852353 | CTGTTTTTTGAATTA[A/G/T]GGTCCAAATAACATC | 83860 |
rs58524937 | snp | G/T | 0.34989 | 0.229177 | intron-variant | TAF3 | GRCh38.p7 | 10:7833052 | GTGGTGCTATTAAAG[G/T]CTGAATAGTATTCTG | 83860 |
rs58526566 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994789 | CCAACATGGTGAAAC[C/G]CTGTCTCTACTAAAA | 83860 |
rs58555368 | in-del | -/AAAAAAAAAAAAA | 0.493318 | 0.0574159 | intron-variant | TAF3 | GRCh38.p7 | 10:7975071 | ACAAGACTCTGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAGAGTGA | 83860 |
rs58593612 | in-del | -/GTATGTATGTATGTATGTAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878725 | TATGTATGTATGTAT[-/GTATGTATGTATGTATGTAT]ATGAGACAGAGTCTT | 83860 |
rs58756353 | in-del | -/C | 0.317451 | 0.240729 | intron-variant | TAF3 | GRCh38.p7 | 10:7938545 | CTGAGAGAATTTGAA[-/C]GGCCAGTCAGACAAA | 83860 |
rs58825999 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988601 | AAAAAAAAAAAAAAA[-/A]GAAGCCAGATATAAT | 83860 |
rs58909843 | snp | C/T | 0.318896 | 0.240319 | intron-variant | TAF3 | GRCh38.p7 | 10:7932398 | AGATAGCACACATGC[C/T]GGAAGTACTGATTCA | 83860 |
rs58910610 | in-del | -/TCTC/TCTCTC | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7957827 | CTCTCTCTCTCTCTC[-/TCTC/TCTCTC]GATGTTGGAACACAG | 83860 |
rs59034943 | snp | A/G | 0.272511 | 0.248984 | intron-variant | TAF3 | GRCh38.p7 | 10:7845452 | CTGGGCAGTGCTAGG[A/G]GTAGGGGTGAACCCA | 83860 |
rs59148597 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7942777 | TTGTGATGTTTTAGT[A/G]AAGGCAGGAAATTTA | 83860 |
rs59207049 | in-del | -/GA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925815 | AAAAAAAAAAAAGAA[-/GA]AAGAAAAGAAAAGAA | 83860 |
rs59228967 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7921107 | TTAAGGTTTTTTTTT[A/T]ACTCTTTCTTTACTG | 83860 |
rs59268670 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | TAF3 | GRCh38.p7 | 10:7886718 | ACCTTACTCCTAATA[C/T]GCATTTTAACCTCAA | 83860 |
rs59389628 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821910 | AGAGAATCACATAAA[A/C]TAAGCTGTCCAGGTG | 83860 |
rs59454036 | snp | A/G | 0.361894 | 0.223562 | intron-variant | TAF3 | GRCh38.p7 | 10:7902747 | ATGTTCTGATCCTCC[A/G]CGTTCATTTAGCATT | 83860 |
rs59502450 | in-del | -/CACACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006217 | ACACACACACACACA[-/CACACACA]AATTAGCTGGGCGTG | 83860 |
rs59519247 | in-del | -/AT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998263 | TATATATATATATAT[-/AT]GTATATATATATATA | 83860 |
rs59627847 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988445 | AAATACAGAAATTAC[A/C]CCTGTTATCCCAGCT | 83860 |
rs59658917 | in-del | -/TATATATATATATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007597 | ATATATATATATATA[-/TATATATATATATA]CCTTTTTTTTTTAAT | 83860 |
rs59711440 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994736 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACAAGGT | 83860 |
rs59722725 | snp | A/G | 0.499866 | 0.0081858 | intron-variant | TAF3 | GRCh38.p7 | 10:7925813 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 83860 |
rs59864228 | in-del | -/CACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974167 | ACACACACACACACA[-/CACACA]AACACACACACGAGA | 83860 |
rs59915097 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TAF3 | GRCh38.p7 | 10:8002293 | TTTCATTGATATCCC[A/G]TATTTCTCTCACCTG | 83860 |
rs59969868 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829057 | AAAAAAAAAAAAAAA[-/A]GGAATATAAACCATG | 83860 |
rs60052409 | in-del | -/GT/GTGG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944136 | TGTGTGTGTGTGTGT[-/GT/GTGG]TGTGGGGGGGAGGGA | 83860 |
rs60053635 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956330 | CATCTCTACTAAAAA[A/C]AAAAAAGTTAGCCAG | 83860 |
rs60116485 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7978762 | TCCATCATTCAACAA[A/G]TACTTTTCTCCTGCA | 83860 |
rs60159100 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7902485 | AGAGTCCGGGCCAAT[A/G]TTGACTGCGTGTGGT | 83860 |
rs60169588 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845977 | TTTTTTTTTTTTTTT[-/T]GAGGCAATGTCTCGC | 83860 |
rs60287426 | in-del | -/GTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920328 | TGTGTGTGTGTGTGT[-/GTGT]ATGTGTGTGTGTGTG | 83860 |
rs60379606 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7961936 | CTCATTGCAGCCTCA[A/G]CCTTCTGGGCTCAGG | 83860 |
rs60390149 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994786 | TGGCCAACATGGTGA[A/G]ACCCTGTCTCTACTA | 83860 |
rs60415433 | in-del | -/AAAAAAAAA/AAAAAAAAAA/GAAAAAAAAA | 0.488606 | 0.0746142 | intron-variant | TAF3 | GRCh38.p7 | 10:7946727 | ACCCTGGTCTCAAAC[lengthTooLong]GAAAAAAAAAGAAGG | 83860 |
rs60450949 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:8005541 | TACACCTTCCACTTC[A/G]GGCAGATCCTGGGCT | 83860 |
rs60531888 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | TAF3 | GRCh38.p7 | 10:7998117 | GGAAAAATGGGTTAC[G/T]TTAGTGCCTCTACAC | 83860 |
rs60595519 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956329 | TCATCTCTACTAAAA[A/C]CAAAAAAGTTAGCCA | 83860 |
rs60689553 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7913700 | TCTGCTTACATCAAC[A/C]CATTGATGAATCTTG | 83860 |
rs60861498 | snp | C/T | 0.299158 | 0.245119 | intron-variant | TAF3 | GRCh38.p7 | 10:7834875 | TTTTACCGTGTGTAT[C/T]TTGTCAGATCATATA | 83860 |
rs60883736 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7884507 | TTCTCCTGTCTCAGC[A/C]TCCCGAGTAGCTAGG | 83860 |
rs61019189 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | TAF3 | GRCh38.p7 | 10:7963058 | TGCCGTAACTCTAGC[C/T]GAAAAACCATTTGTC | 83860 |
rs61078038 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | TAF3 | GRCh38.p7 | 10:7981686 | TTCTGGTGGCAAGTG[A/G]ATTGATTTCTTACAA | 83860 |
rs61165434 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974171 | ACACACACACACACA[-/CA]AACACACACACGAGA | 83860 |
rs61197796 | snp | A/G | 0.356811 | 0.226034 | intron-variant | TAF3 | GRCh38.p7 | 10:7862691 | CTTCCCTCCTCCCCA[A/G]GGGGATCCCCAGGCA | 83860 |
rs61269269 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7942744 | CAGCCGAGGCGTGTG[C/G]GCACGGAGTTCTAGA | 83860 |
rs61367638 | in-del | -/TATATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007605 | ATATATATATATATA[-/TATATA]CCTTTTTTTTTTAAT | 83860 |
rs61498355 | in-del | -/TTTTTTTTTTTT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7884403 | CTCCTTTTTTTTTTT[-/TTTTTTTTTTTT]GAGATGGAGTTTTGC | 83860 |
rs61603836 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | TAF3 | GRCh38.p7 | 10:7885197 | TAATCAAGCCACTGA[A/T]TTGCATACTTAAAAA | 83860 |
rs61731331 | snp | A/T | 0.00709051 | 0.0591184 | missense | TAF3 | GRCh38.p7 | 10:7964498 | AAGGTCACGACTCAC[A/T]TTCCCCAAACACCTG | 83860 |
rs61731332 | snp | A/G | 0.00126124 | 0.0250805 | missense | TAF3 | GRCh38.p7 | 10:7964873 | CCTCTGCCTCTTTCC[A/G]GTGGAACCTCAAGTT | 83860 |
rs61833206 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817151 | TGTGAAATCCAAGGC[A/G]CAAGAGAGTTTCAAT | 83860 |
rs61833207 | snp | A/C | 0.325799 | 0.238232 | intron-variant | TAF3 | GRCh38.p7 | 10:7825565 | GTCTATTCTAGGTAC[A/C]TTTTATAAATGGACT | 83860 |
rs61833209 | snp | A/G | 0.122411 | 0.214991 | intron-variant | TAF3 | GRCh38.p7 | 10:7835396 | GCTCCCTCTTCTATC[A/G]TTTTTGCGGAATGTT | 83860 |
rs61833210 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7839015 | CTGATGTTGGGATAT[A/G]CCTGTGGTGTTCAGT | 83860 |
rs61833211 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7841501 | CTCTAACCTAGTGTG[C/T]TTACAGGAATAAGGG | 83860 |
rs61833218 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | TAF3 | GRCh38.p7 | 10:7850087 | AAATATAGATCCTCG[C/T]ATTTCCTGATAAGTC | 83860 |
rs61833219 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7851196 | AAAAATATGCTAGTC[A/G]GGGGAACTAGTGAGA | 83860 |
rs61833220 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7851217 | ACTAGTGAGAAAGCA[A/G]CATTCTAGCAAAGAC | 83860 |
rs61833222 | snp | A/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7887230 | GAGCCAGACTCTGTA[A/T]TTAAAAAAAAAAAAA | 83860 |
rs61833223 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888403 | TATAAAAAAAAAGTT[A/T]CTTGAATATTTTGAT | 83860 |
rs61833240 | snp | A/G | 0.440609 | 0.161766 | intron-variant | TAF3 | GRCh38.p7 | 10:7935257 | ACTCCAGCCTGGGCA[A/G]CAGCAAAACTCTGTT | 83860 |
rs61833256 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7946169 | TAAAACTACCGGTGA[A/C]TTCCTATACCCTTCA | 83860 |
rs61833259 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7969199 | AATTAACTAGGCATG[G/T]TGTTGCACATCTGGA | 83860 |
rs61833460 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990346 | CATTTAAAGCCAAGT[G/T]AGCAAGGCAGAATGG | 83860 |
rs61835860 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971226 | ATTTTAAATAGTTAT[C/T]AGAGTTTACTTAGAC | 83860 |
rs61835861 | snp | A/C | 0.45946 | 0.136478 | intron-variant | TAF3 | GRCh38.p7 | 10:7976405 | GCACCCGCCACCATG[A/C]CTGGCTAATTTTTTT | 83860 |
rs63742761 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971467 | GTTTTTTTTTTTTTT[A/T]AATGAAAGGAGTTTA | 83860 |
rs66738509 | snp | A/G | 0.170733 | 0.237101 | intron-variant | TAF3 | GRCh38.p7 | 10:7839619 | CTCAAGGGCACAGAT[A/G]GAAGAACAAAGGCTT | 83860 |
rs66755455 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7855662 | TACTCAAAGCTCCCA[C/G]ACAGCTTTTTTAGTT | 83860 |
rs67672545 | snp | C/T | 0.249038 | 0.249998 | intron-variant | TAF3 | GRCh38.p7 | 10:7992271 | GGAACCCTCAAAGTA[C/T]CCCAGACAACACTCT | 83860 |
rs71287400 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7994995 | AGGATTTCTTTTTTC[-/T]TTTTTTTTTTTTTTT | 83860 |
rs71287402 | in-del | -/CTTTGCACCC | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7831950 | TAAAACATAACATCG[-/CTTTGCACCC]CTTTGCACCCCCCAG | 83860 |
rs71385674 | in-del | -/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7832224 | AGAGTAGAACAGTGG[-/T]TTACAGAGGCTGGGG | 83860 |
rs71385678 | in-del | -/GT | 0.466927 | 0.124269 | intron-variant | TAF3 | GRCh38.p7 | 10:7885249 | TGTGTGTGTGTGGGG[-/GT]GTGTGTGTGTGTGTG | 83860 |
rs71385679 | in-del | -/TCAGTCTAGGTTTAAAAAAAAAAGTGAACACCTGGAAAGAT | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7901014 | CTAATTTTTGGATGA[lengthTooLong]TCACCACAAGCACAC | 83860 |
rs71385681 | in-del | -/GT | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7939621 | GGGGTGTAGGTAGAG[-/GT]GTGTGTGTGTGTGTG | 83860 |
rs71385686 | in-del | -/A | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7993904 | TGAAGACTGGCAAGT[-/A]AAAAAAAAAAAAAAA | 83860 |
rs71477297 | in-del | -/A | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7985801 | GTGAGATTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 83860 |
rs71477299 | in-del | CGCGCGCGCG/GGCGCGCGCACA | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7858825 | ATTCAGTGACATGCA[CGCGCGCGCG/GGCGCGCGCACA]CACACACACACACAC | 83860 |
rs71481743 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819147 | TACCGCTCCTCCGCT[C/T]TGAATTGTGTCTGGA | 83860 |
rs71481744 | snp | G/T | 0.375 | 0.216506 | intron-variant | TAF3 | GRCh38.p7 | 10:7842187 | TTTTGTTTTTTTTTT[G/T]TTTTGAGACAGAGTC | 83860 |
rs71481745 | snp | A/G | 0.112631 | 0.208878 | intron-variant | TAF3 | GRCh38.p7 | 10:7867034 | GAGGCCGAGGCAGGC[A/G]GATCACCTGAGGTCA | 83860 |
rs71481746 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7919740 | GTAGTCTTTATACTG[G/T]TTTTATTGCTATTAT | 83860 |
rs71481747 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7932698 | TTTTTTTTTTTTGGA[A/G]AGAGGGTCTTGCTCT | 83860 |
rs71481748 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7941813 | GTGCTTGGTCTTAGA[A/G]AGCCTGGAGCATGTG | 83860 |
rs71481749 | snp | A/G | 0.107694 | 0.205546 | intron-variant | TAF3 | GRCh38.p7 | 10:7943455 | ACTTGCTGAGTGGGA[A/G]CCCCTCTTTTGCCAG | 83860 |
rs71481750 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954224 | TTAACACAGAGCTCT[C/T]CCTAGTGAGATTCAG | 83860 |
rs71481751 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | TAF3 | GRCh38.p7 | 10:7992200 | GAGCAGCAAAAGCCT[C/T]TCTGAAATCACAAAA | 83860 |
rs71487533 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7863646 | ATATATATATATATA[C/T]ACACACACACATATA | 83860 |
rs71505463 | in-del | -/TTTTTTTTTT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7838923 | TTTTTTTTTTTTTTT[-/TTTTTTTTTT]GGTTTGTTTGTTTTG | 83860 |
rs71505464 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | TAF3 | GRCh38.p7 | 10:7839693 | CAATTATTTTTTTTT[-/T]AATTGTGTTTTGTTA | 83860 |
rs71505465 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7842152 | ATTGAATTAATATTG[-/T]TTTTTTTTTTTGTTT | 83860 |
rs71505466 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7842165 | TTGTTTTTTTTTTTG[-/T]TTTTTTTTTTGTTTT | 83860 |
rs71505467 | in-del | -/A/AA | 0.49607 | 0.0441545 | intron-variant | TAF3 | GRCh38.p7 | 10:7856859 | AACAGCTGGTTCTCA[-/A/AA]AAAAAAAAAAAAAAA | 83860 |
rs71505468 | in-del | -/GTTAAG | 0.499527 | 0.0153681 | intron-variant | TAF3 | GRCh38.p7 | 10:7857779 | GATGTTTTTGTTAAG[-/GTTAAG]AAAGAAAAAGGCAGG | 83860 |
rs71505469 | in-del | -/GTATGTATGTATGTAT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7878729 | TATGTATGTATGTAT[-/GTATGTATGTATGTAT]ATGAGACAGAGTCTT | 83860 |
rs71505470 | in-del | -/T | 0.443195 | 0.158668 | intron-variant | TAF3 | GRCh38.p7 | 10:7884995 | TTAATTTTTGTTCAG[-/T]TTTTTTTTTTTAATT | 83860 |
rs71505471 | in-del | -/GTGTGTATGTGTGTGTGTGTGTGT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7920326 | TGTGTGTGTGTGTGT[-/GTGTGTATGTGTGTGTGTGTGTGT]AAATGCTTGGTTCAT | 83860 |
rs71505477 | in-del | -/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8010805 | ATCCCAGCTACTCGG[-/G]AGGCTCAGGCACAAG | 83860 |
rs71515490 | in-del | -/T/TT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7823635 | TTTTTTTTTTTTTTT[-/T/TT]CTGAGATGGAGTCTT | 83860 |
rs71515491 | in-del | -/AAA | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7827796 | AAAAAAAAAAAAAAA[-/AAA]CAAAAACAAAAACTT | 83860 |
rs72638739 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | TAF3 | GRCh38.p7 | 10:7871806 | GTAAAAATTCATACA[G/T]TTAATGAATTAGATT | 83860 |
rs72638740 | snp | G/T | 0.102014 | 0.201495 | intron-variant | TAF3 | GRCh38.p7 | 10:7917812 | GAAGTTATATAAGAT[G/T]AAAACTGAAAATGGA | 83860 |
rs72638741 | snp | A/G | 0.116488 | 0.211364 | intron-variant | TAF3 | GRCh38.p7 | 10:7967716 | GGTGTGCTTAGTACC[A/G]TATCTGACGCATAAA | 83860 |
rs72638742 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | TAF3 | GRCh38.p7 | 10:7983222 | CCGTTATCAGCCCCC[A/G]TGAAGGACTTCGCTT | 83860 |
rs72781098 | snp | C/T | 0.399611 | 0.200291 | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818275 | GTCGTATCCCAGATC[C/T]CTCGTTTGCCTCTAA | 83860 |
rs72781101 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7821400 | GAGCATCACTTACGA[A/G]CCAACCCCTGTACTA | 83860 |
rs72781102 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7821550 | CAAGTTAAAGCAAGT[A/G]TTAGAAGTTACCATT | 83860 |
rs72782704 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TAF3 | GRCh38.p7 | 10:7822645 | CATTACTACACATGC[A/G]TCCAATTCTAGCAAT | 83860 |
rs72782707 | snp | A/G | 0.350327 | 0.228986 | intron-variant | TAF3 | GRCh38.p7 | 10:7838865 | CAGGGTCTGGGGAAC[A/G]TTCCTTCTGTGTATC | 83860 |
rs72782712 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7845546 | TGGAAGCGAGAATGT[A/G]TTTGAGATAGGTGGT | 83860 |
rs72782716 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | TAF3 | GRCh38.p7 | 10:7846833 | ATGCTAAAAAAGACT[A/G]AAATAATAAGTGGAA | 83860 |
rs72782723 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | TAF3 | GRCh38.p7 | 10:7867495 | GAAATTAGCCCATTT[G/T]TGTTTGTTTTGCCTT | 83860 |
rs72782734 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7877070 | CCACGTCTGAGGTTT[A/G]TTTTTTACGCTGTTA | 83860 |
rs72782738 | snp | G/T | 0.326976 | 0.237854 | intron-variant | TAF3 | GRCh38.p7 | 10:7883732 | CACTTATTTATTCAT[G/T]TATTGATATCCGCAG | 83860 |
rs72782739 | snp | A/G | 0.342358 | 0.232314 | intron-variant | TAF3 | GRCh38.p7 | 10:7884190 | GTAGCATACTCCTTT[A/G]CTGTTATTATTTATT | 83860 |
rs72782744 | snp | C/T | 0.324382 | 0.238678 | intron-variant | TAF3 | GRCh38.p7 | 10:7888136 | CACACTCAGATCTCT[C/T]CCATATGAAACGTTT | 83860 |
rs72782782 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7981658 | TTAGTTTTCTTTCTG[C/T]TGACATTTTGATTTC | 83860 |
rs72782784 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | TAF3 | GRCh38.p7 | 10:7995555 | AGAGATTTTATGATT[C/T]GGAACATTTGACAAT | 83860 |
rs73616012 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7830301 | CTCAGAATAGCTTCT[A/G]TGTGCCCAACCCCAC | 83860 |
rs73616017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831956 | GGGTGCAAAGCGATG[C/T]TATGTTTTATAAATA | 83860 |
rs73616020 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7836602 | TCTTACCACGAATAC[A/T]CCTGTGTTATCCATC | 83860 |
rs73616049 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7863125 | AAACTGTGGTGGACT[A/G]ACTTCTTGGAAGTAG | 83860 |
rs73616056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7903642 | TTAGCATTGCACCAT[A/G]TATGAAAAATTAGAA | 83860 |
rs73616084 | snp | A/G | 0.308908 | 0.242961 | intron-variant | TAF3 | GRCh38.p7 | 10:7983019 | AAATCAAACCGTCTT[A/G]GAGGGGAAAACAGCA | 83860 |
rs73616096 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7994140 | ATGTTCATATTGTAC[C/T]ATCTTGACCAACGTG | 83860 |
rs73618922 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | TAF3 | GRCh38.p7 | 10:8007766 | CTTCTTTGATGTTCT[C/G]ATAAGGACTGGATGA | 83860 |
rs73618926 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | TAF3 | GRCh38.p7 | 10:8007969 | AGTTGTGTGAAGAGG[A/T]TGCTGTTAGTGGAGG | 83860 |
rs74123639 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7854036 | AAGAAACACACACAC[A/G]ATCATTCGCCCCACT | 83860 |
rs74123640 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7854062 | CCACTCAGCCAGTTG[G/T]TAAACATTTACCAGC | 83860 |
rs74123643 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7893460 | TGCAAGTTCTGTCTA[C/T]GTCGTGACCCATCAG | 83860 |
rs74123644 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7899581 | TGCAGCTTTGTGCTT[G/T]GTACTGGAAGGTTAA | 83860 |
rs74123646 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7899786 | GGGATGTGCTCTATA[A/G]TATGTTGTAAAAATA | 83860 |
rs74123647 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7901828 | AACTTTGTTTTTTCA[A/G]AAAATAGGTATTTTC | 83860 |
rs74123809 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7926970 | TCTAGGGGTTGAGAA[C/T]CCAAAGATGAAAGTG | 83860 |
rs74123815 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7940634 | AGTTCTTGTAAAGTA[A/G]ATAAGAAAAAAAGCA | 83860 |
rs74123817 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7944404 | TCAGTAAGACCATCA[A/G]CAGACTAATTATTCT | 83860 |
rs74123826 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7968237 | AAAATGTTTTCAGCC[A/G]AAAGAATGAAGGCCA | 83860 |
rs74123827 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | TAF3 | GRCh38.p7 | 10:7970748 | TAATGTTTCTTTATC[A/C]CCAAGTCCTGTAGGA | 83860 |
rs74123828 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | TAF3 | GRCh38.p7 | 10:7983162 | CTCAGGCTGTTGTGA[C/T]TCTTGGTGCTCACAG | 83860 |
rs74123833 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | TAF3 | GRCh38.p7 | 10:8010326 | CTTGTTTTTATATTG[G/T]TTTGGGATATGACTA | 83860 |
rs74230014 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970806 | TTTAAACGGTTTGTT[C/T]TTTAGAGAATGATAA | 83860 |
rs74317482 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7901729 | TCTTAAATTAATATT[G/T]TATATTAAGACGCTT | 83860 |
rs74342746 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7939828 | TGAGAAAACTACAGA[A/G]TTAATTCATGAGGTC | 83860 |
rs74381490 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7973634 | ATGTTTGTTTTTTAA[A/C]AACCTTAATGAGCAC | 83860 |
rs74406825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8002204 | CTGAAAACGCCTGGG[C/T]TGTCCTCACACTTCC | 83860 |
rs74407628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7986123 | CCTTTTGTTTTTCTT[C/T]TATGGACTTATTTTT | 83860 |
rs74414169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984687 | GGAAACTTTCTCTCC[A/G]CAGTGTTATCAAGGT | 83860 |
rs74414607 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7887243 | TATTTAAAAAAAAAA[A/G]AAAAAGAAAGAAAGC | 83860 |
rs74421449 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7975818 | ATTTTATGTGTTCCC[C/G]TTTAGAACCACTATA | 83860 |
rs74443041 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885274 | CACACACACACACAC[A/C]CCCACACACACACAA | 83860 |
rs74467725 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7892835 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTCTCT | 83860 |
rs74498820 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7892833 | CTTTTTTTTTTTTTT[G/T]TGAGACGGAGTTTCT | 83860 |
rs74512967 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7909280 | TAGTTGATTCTTGTA[C/T]ATGCTGAAGTTTGAG | 83860 |
rs74514054 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7869719 | AAAGGCTGTCCCAGC[A/G]TGCACCCCTGCAGCA | 83860 |
rs74529136 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8013422 | ATAGTTTTTTTTTTT[A/T]TGAAAGGGGTTACAG | 83860 |
rs74542993 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TAF3 | GRCh38.p7 | 10:7977076 | ATGATGCCAGGTAGC[C/T]TTCAGTTGTACAGAA | 83860 |
rs74554559 | snp | A/G | 0.138546 | 0.223781 | intron-variant | TAF3 | GRCh38.p7 | 10:7876738 | TATCTTTGGAGCATA[A/G]CCAAAGTCATTATTT | 83860 |
rs74556236 | snp | G/T | 0.127599 | 0.217986 | intron-variant | TAF3 | GRCh38.p7 | 10:7831264 | ATAAATTGGTTCCTT[G/T]TTATCCTTAGCAGGT | 83860 |
rs74578588 | in-del | -/AAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898564 | AAAAAAAAAAAAAAA[-/AAA]AAAAAATCGAACTCT | 83860 |
rs74608380 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7979406 | TATTCAACTCACCTG[C/T]CTTTAAGCATCTTTC | 83860 |
rs74613900 | snp | A/T | 0.0711525 | 0.174681 | intron-variant | TAF3 | GRCh38.p7 | 10:7996646 | TTGTTGTGAGGGGGG[A/T]TTTTTTTGTGTTATC | 83860 |
rs74652496 | snp | G/T | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819698 | TGAAGCATTGTATGT[G/T]TGTTTGTTGAGGAGA | 83860 |
rs74674053 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869924 | TTGCCTCTTTTATCA[C/G]GCCTGACCCCTGGGT | 83860 |
rs74678290 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7877924 | GTAACGGCAATTCAG[A/G]TCTCAAATACATTGG | 83860 |
rs74683464 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7983622 | GAGTTTTATTTTTCC[A/C]TGATTAACTTGCTAC | 83860 |
rs74687101 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7876084 | CTTATAATTTATCTT[C/G]TCTGTATAATAAAGG | 83860 |
rs74687477 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7860290 | GGAAAAAAAAAAGAA[A/G]AAAAAAAAAAAGAAA | 83860 |
rs74694365 | snp | A/G | 0.103438 | 0.202533 | intron-variant | TAF3 | GRCh38.p7 | 10:7825056 | GTTTGATCATATAGA[A/G]CTTTTGATTATAAAA | 83860 |
rs74749280 | snp | A/T | 0.0327778 | 0.123752 | intron-variant | TAF3 | GRCh38.p7 | 10:7872576 | TGGTTCTATCTTGAG[A/T]AATAGCAGAGTTAAT | 83860 |
rs74832960 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:8004569 | GTTTTCAAAGACATA[A/G]TTTATTTTTCTTTAG | 83860 |
rs74846163 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | TAF3 | GRCh38.p7 | 10:7963308 | TGCATGAGAGAGAGA[G/T]AGAGAAAGATGGCAT | 83860 |
rs74848266 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7912296 | ATGGAGACAGGGTCC[C/G]ACGATGTTGCCCAAG | 83860 |
rs74848974 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:8001582 | GCCATATAAAATTGT[C/T]GTGCAGTCAAATCAG | 83860 |
rs74851498 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:8009000 | AAGAAAAGCTATTTT[A/C]CGATCATGTTTTTAA | 83860 |
rs74880836 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7928938 | TCATCTCCACAGAAG[A/T]ATTTTTTTTAAGTGT | 83860 |
rs74913168 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954565 | AACACAGAGCTCTCC[A/C]TAGTGAGATTTAGAG | 83860 |
rs74938738 | snp | A/C | 0.0707826 | 0.174302 | intron-variant | TAF3 | GRCh38.p7 | 10:7995410 | GCCTTTTTCCCTATG[A/C]CCTTTATACTCCTTA | 83860 |
rs74946951 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7834267 | GCCAAATATAAAAAA[C/T]AATTGCCCAGACCAG | 83860 |
rs74947864 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7948079 | GATTTTTTTTTTTTT[G/T]GGAGACAGGGTCTCA | 83860 |
rs75022641 | in-del | -/TGTATGTATGTATGTAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878728 | GTATGTATGTATGTA[-/TGTATGTATGTATGTAT]ATGAGACAGAGTCTT | 83860 |
rs75048866 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7867490 | GCTCTGAAATTAGCC[C/T]ATTTGTGTTTGTTTT | 83860 |
rs75049151 | in-del | -/GTGC | 0.38286 | 0.211774 | intron-variant | TAF3 | GRCh38.p7 | 10:7828900 | TGGGTGTGGTGGTGC[-/GTGC]CTGTAGTCCCAGCTA | 83860 |
rs75063993 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | TAF3 | GRCh38.p7 | 10:7854904 | AGCAAAAGTGGTATT[C/T]GTTAAACACTTTTGA | 83860 |
rs75074398 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7977825 | TCACAACTGATGACT[C/T]AGTCCACTTTTTTTT | 83860 |
rs75077228 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7946092 | TCGGGTCATCCATAA[C/T]GTCACTGCATCCTCT | 83860 |
rs75083134 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | TAF3 | GRCh38.p7 | 10:7943076 | CCGAAAGTCTGTCCT[G/T]ACTTAGCAGCGGTTG | 83860 |
rs75109422 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7900791 | ACTGAACTTTTTGCT[C/T]TTTAGGCTTCGTATT | 83860 |
rs75113246 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7853477 | GTAGATTAAACTTCA[A/G]AATGTATAGTATCTG | 83860 |
rs75115524 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7929745 | AACATTACCAATAAA[C/T]AAGAATATGGAGTAC | 83860 |
rs75126656 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7990169 | CAACTGAGAAATGCT[A/G]CTTGATCTGTATATG | 83860 |
rs75134641 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:8006014 | AAAGCAGAATAATAG[A/C]TTGCCTCATGTGGTC | 83860 |
rs75148279 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7879020 | GGCATAAGTCACCGC[A/G]CCTGGCAAATTCAAC | 83860 |
rs75172323 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954330 | TCCATAGGCGAATGA[A/G]TGAATTAGTTCTAGT | 83860 |
rs75200268 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:8001746 | CGTTTAGAATTTATG[G/T]TTTGTGATACAGCTC | 83860 |
rs75213081 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954323 | AGTGCACTCCATAGG[C/T]GAATGAGTGAATTAG | 83860 |
rs75222908 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7928529 | AACATATTTTGCCTG[C/T]TGACTCAAGGGTGTC | 83860 |
rs75228569 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7971314 | TACAGCCATAGTTCA[A/G]CATCCAAATGTTAGG | 83860 |
rs75288759 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7885520 | ATTTCCCTCCTCACC[A/G]AATCCTTTCCACTTG | 83860 |
rs75295135 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7968112 | CCTACAAATCTACAG[A/C]AGTAAGGCACCAAAG | 83860 |
rs75346048 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | TAF3 | GRCh38.p7 | 10:7907273 | GGGCTGTCATTGGTG[C/T]GACTTAGATCACAGA | 83860 |
rs75347982 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7974633 | CTATAATGGGAAAAC[C/T]GGGACATGAGGACAT | 83860 |
rs75354228 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7892832 | TCTTTTTTTTTTTTT[G/T]TTGAGACGGAGTTTC | 83860 |
rs75382569 | snp | A/G | 0.108402 | 0.206034 | intron-variant | TAF3 | GRCh38.p7 | 10:8010365 | TATACAGTAATATCA[A/G]TCTGTAAATGTAGAG | 83860 |
rs75394792 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7845241 | AATGTGGGAACTACC[A/C]AAAAAAAAAAATCTC | 83860 |
rs75398800 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7948276 | TTTTTTTTTTTTAGA[G/T]ACAAGATCTTTCTTG | 83860 |
rs75398826 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7948443 | ATGTGATAACTTTCT[A/G]TTATTACTCATAGAT | 83860 |
rs75436442 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7860291 | GAAAAAAAAAAGAAG[A/G]AAAAAAAAAAGAAAA | 83860 |
rs75447938 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | TAF3 | GRCh38.p7 | 10:7949832 | ACATAGAAGGGTTGC[A/C]GTGGCCAGTCATTCT | 83860 |
rs75469814 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7864385 | TATAGGCACTGTGGA[A/G]TGGTTAACTCTAACA | 83860 |
rs75489070 | snp | A/G | 0.100944 | 0.200705 | intron-variant | TAF3 | GRCh38.p7 | 10:7833911 | GCCGCTGCACAGTGC[A/G]TGTGGAAGTGGGGCT | 83860 |
rs75492525 | snp | C/G | 0.341685 | 0.232581 | intron-variant | TAF3 | GRCh38.p7 | 10:7897654 | TCCTATTCTCTCTCT[C/G]TCTCTCTTTCTTTCT | 83860 |
rs75501993 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7824663 | AATTCTGGAAACACA[A/G]TAGAAACATTTACTG | 83860 |
rs75503237 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | TAF3 | GRCh38.p7 | 10:7845210 | TGTGTCATTTTGTTT[C/T]AAAATTTTTAGTTGA | 83860 |
rs75508103 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7936065 | GTGTCCTGGACTAGT[A/G]TGATTGTATCGTAAA | 83860 |
rs75536690 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7911981 | CCAGGCTACCACAAC[A/G]AGTCATATGCACTTT | 83860 |
rs75580058 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7935782 | CGCAGATTCCAGGCC[C/T]TGAGGCTGAAGACTT | 83860 |
rs75612161 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7991097 | GTGAATCTGAAGTCA[A/G]TGTAATAATTTCAGT | 83860 |
rs75618774 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | TAF3 | GRCh38.p7 | 10:7856739 | TGACTTGGAACATTT[C/T]GTTATACCAAGTAGC | 83860 |
rs75642423 | in-del | -/TTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971465 | GTGTTTTTTTTTTTT[-/TTT]AATGAAAGGAGTTTA | 83860 |
rs75672702 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934153 | ATTAGAAACTGAAAG[A/G]AAAGAACTTTTAGGA | 83860 |
rs75682795 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7835705 | CTCGGGTTGGCCTGC[C/T]GGGCTTTCCAGCAGA | 83860 |
rs75735153 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7878545 | GGCCACACACTTAGG[A/G]TATATTAACTTTGTA | 83860 |
rs75817313 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:8008671 | ACAGGCTGCTCCAGG[A/T]CCTCTCCAGCTGGAG | 83860 |
rs75838269 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885862 | ATGTTATTATTTTTG[A/T]TTACCTGTTTTTAGG | 83860 |
rs75850426 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | TAF3 | GRCh38.p7 | 10:7883936 | AGAGTCACCAGGCAA[C/T]GCAGGGCATCACATG | 83860 |
rs75889834 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:7993873 | AGAGGCAGGATAAAT[A/G]TACAATCTTTTTTTT | 83860 |
rs75924294 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | TAF3 | GRCh38.p7 | 10:7973075 | ACTAACTTTGTAACT[C/G]TAGGTAAAGCACTTA | 83860 |
rs75929573 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7847455 | CATGTGTTTAAATTC[C/T]TTTTTTTAAGACAGA | 83860 |
rs75930726 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7963174 | AGTATATGAATTTGT[C/T]ATAAAAGTCCTAAAA | 83860 |
rs75937072 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954536 | ATAGGCGAATGAGTG[A/G]ATTAGTTCTAGTTAA | 83860 |
rs75945516 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7825662 | TGTTGTAGCCTGTGT[C/T]GGGATTTCGTTGTGT | 83860 |
rs76007192 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | TAF3 | GRCh38.p7 | 10:7999342 | ATCTGCACACAACTG[A/G]GACACAAAGCAACTA | 83860 |
rs76013127 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7945793 | GTCCTGTCTAAAGTC[G/T]CCCTTTTTCTCTCCA | 83860 |
rs76017643 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | TAF3 | GRCh38.p7 | 10:7996271 | AAGCTCACGCACAGC[C/T]GTCGGCAGGAGGCTC | 83860 |
rs76027842 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873462 | TTGAGGAACCTGTCA[A/T]GTAATTTTAGAAAAA | 83860 |
rs76027864 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7899974 | GATTGCCTTTCCCCT[C/T]GTTTTCCTCAGTGGA | 83860 |
rs76039144 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7850930 | TTCTTTCAGCACATA[C/T]TTATTGTTCTCTGAT | 83860 |
rs76069666 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7971382 | TTTTTTCTAACATAC[C/T]GGCATAGATGGGAAT | 83860 |
rs76109057 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7862613 | GCATTGTCACAGTCA[A/G]AATTATGAAGATATC | 83860 |
rs76121713 | snp | G/T | 0.030665 | 0.119967 | intron-variant | TAF3 | GRCh38.p7 | 10:7888038 | ACCCATCTGTCCAGC[G/T]TAGGTTCCCTTGCTC | 83860 |