SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs76125144 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | TAF3 | GRCh38.p7 | 10:7861627 | CAGATATTTTTCCAC[A/C]ATCTCATAACCTCCA | 83860 |
rs76143292 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930931 | AGGATCTTTATAAGT[C/T]CCACAAGTTTGTCTT | 83860 |
rs76161055 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7975373 | CATGCTTTACACTTA[C/T]CTTAAGACTTACTAG | 83860 |
rs76183298 | snp | A/G | 0.110167 | 0.207236 | intron-variant | TAF3 | GRCh38.p7 | 10:7823885 | TGATCCGCCCACCTC[A/G]GCCTCTCAGTGCTGG | 83860 |
rs76201196 | snp | A/G | 0.115088 | 0.210473 | intron-variant | TAF3 | GRCh38.p7 | 10:7854401 | ACTGTTATGCGAGCC[A/G]CAGCGAGATACACAC | 83860 |
rs76206367 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7994235 | TTCTGGTAAAAAAAA[A/T]TTCCAGGTTTATCTT | 83860 |
rs76215284 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7928271 | AACTCACTGCCGTGT[C/T]CCAGTACCTGATACC | 83860 |
rs76231018 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7836295 | TTCTTTTTTCTTTCT[C/T]TTTTTTTTTTTTGAG | 83860 |
rs76233421 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7951538 | TGTGCAGCCGCTTTC[C/T]ATGCCTCTGCTTCTG | 83860 |
rs76252615 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7842974 | ATAATATCCTCCGGA[A/T]TTCTTTCTAATCTGG | 83860 |
rs76252818 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8003207 | TTCAGTGGTTTTTTT[C/T]CTCTCTCTCTCTTTT | 83860 |
rs76269404 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TAF3 | GRCh38.p7 | 10:7956677 | GGTGATGAATTTGTG[C/T]TGAGTCATTCATGAT | 83860 |
rs76275015 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7979612 | CTTTCAGATATGTAG[A/G]TAATGACTGCCATGT | 83860 |
rs76283038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7942083 | TCAGTTATATCTCAA[A/G]AGGTGACAAGTTGAC | 83860 |
rs76317632 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | TAF3 | GRCh38.p7 | 10:7943542 | GTTCTAGCTGCCAGG[A/G]GTGCCTGAGAGCCAC | 83860 |
rs76320974 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | TAF3 | GRCh38.p7 | 10:7917619 | TAACAAGTGCGCTTG[G/T]CCTGCTCTCTGGAGA | 83860 |
rs76344466 | in-del | -/G | 0.142272 | 0.225598 | intron-variant | TAF3 | GRCh38.p7 | 10:7869526 | ACATAGTTCCCTGTT[-/G]GTGACATTTAGATTG | 83860 |
rs76357762 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873618 | AGACATCCGAGTTCT[-/C]CCCCCCCCCCCGTCA | 83860 |
rs76391303 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | TAF3 | GRCh38.p7 | 10:7897232 | TACCCACACCCAAAG[A/G]GGACGGGATCACACT | 83860 |
rs76408917 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873463 | TGAGGAACCTGTCAT[A/G]TAATTTTAGAAAAAC | 83860 |
rs76425674 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | TAF3 | GRCh38.p7 | 10:7906940 | TCCTAACCTAACAGC[G/T]TGATTCTTATCTAAG | 83860 |
rs76446174 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7905423 | TGTTTTCATACACGA[C/T]GAAAATGTAAGTAAT | 83860 |
rs76467393 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7989889 | ATGTCAACTCTGGCT[C/G]TGATATCATATACTT | 83860 |
rs76476870 | snp | A/C | 0.030665 | 0.119967 | intron-variant | TAF3 | GRCh38.p7 | 10:7822816 | TCATAGACATTTTTA[A/C]AGATGTAGAGACCTT | 83860 |
rs76480652 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | TAF3 | GRCh38.p7 | 10:7861808 | TTTTTCTCAATGCTT[G/T]GGAGTTACTGAACTT | 83860 |
rs76495453 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | TAF3 | GRCh38.p7 | 10:7823221 | ATAGGTATTTATTGA[A/G]TGCCAGCTATGTGCC | 83860 |
rs76522141 | snp | C/T | 0.34146 | 0.23267 | intron-variant | TAF3 | GRCh38.p7 | 10:7885994 | TGTGTAGTGGCGCGA[C/T]GATGGCTCACTACAG | 83860 |
rs76580271 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | TAF3 | GRCh38.p7 | 10:7995821 | TATAGTTGTGTTATA[A/G]TTATATGAATGTTAA | 83860 |
rs76600458 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | TAF3 | GRCh38.p7 | 10:7905515 | AGCTGTGTTACAGCC[C/T]ATTTTTTGAGTGTTT | 83860 |
rs76609621 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7947693 | GCCAGCATGGCTTGA[G/T]GAAGGCAGCTAAGAA | 83860 |
rs76617544 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7916056 | TCTGTTGTATTTATT[A/G]TGTCAGAGGAGTGAA | 83860 |
rs76618254 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7890579 | CAGTACAGTCAAGAC[C/T]CTTTCTGTGAGTGTT | 83860 |
rs76648900 | snp | A/G | 0.030665 | 0.119967 | intron-variant | TAF3 | GRCh38.p7 | 10:7822458 | TTATTTTCTTTTTTT[A/G]ATGCATCACAGAAGT | 83860 |
rs76653315 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7868995 | TTTTTCTAGCAAGGT[C/T]CTTCCAAGATTGGAT | 83860 |
rs76671212 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7833899 | GGTACCCCTTCAGCC[A/G]CTGCACAGTGCGTGT | 83860 |
rs76681064 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | TAF3 | GRCh38.p7 | 10:7995440 | ATTCTATAGGTTGCC[A/G]TTTTGGTTTCCTTTT | 83860 |
rs76698396 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:8011741 | CTCCTTGACCTTCGT[A/G]TCTTCATCTGTAATT | 83860 |
rs76713082 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7861797 | TTCTTTCTTTTTTTT[C/T]CTCAATGCTTGGGAG | 83860 |
rs76715011 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7870852 | TTTAAGATGCTAAAA[G/T]AATGTATTCTAAGCC | 83860 |
rs76728006 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7954001 | AATGAGTGAATTAGT[C/T]CTAGTTAACACAGAG | 83860 |
rs76743768 | snp | A/G | 0.121022 | 0.21416 | intron-variant | TAF3 | GRCh38.p7 | 10:7966120 | ATATTGAGAAAGGCA[A/G]CATCCATGTTTCTAA | 83860 |
rs76765983 | snp | A/T | 0.0707826 | 0.174302 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016461 | TTTTTCTATCCCCGC[A/T]AAGAAACAAAGCATC | 83860 |
rs76774731 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954294 | AACACAGAGCTCTCC[A/C]TAGTGAGATTCAGAG | 83860 |
rs76809517 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | TAF3 | GRCh38.p7 | 10:7968967 | TAGTCAGGGTTGGGA[C/T]TCTAGACTGTCACTT | 83860 |
rs76872652 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936536 | CTTTATTATTTAGAG[C/G]AGTTTTGAGTTCCCA | 83860 |
rs76874042 | snp | G/T | 0.0596104 | 0.162024 | intron-variant | TAF3 | GRCh38.p7 | 10:7834550 | AATATTTATATACAT[G/T]TAGATGTGTGTGAAT | 83860 |
rs76893149 | snp | A/G | 0.359152 | 0.224913 | intron-variant | TAF3 | GRCh38.p7 | 10:7846263 | CGCCCGGCCAAAAGG[A/G]TGAAGTTTTTAAAAA | 83860 |
rs76917742 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001463 | ACATTAATTCTTTTT[-/T]TATTCACAACAGCTG | 83860 |
rs76929952 | snp | A/C | 0.0599851 | 0.162463 | intron-variant | TAF3 | GRCh38.p7 | 10:7989109 | GATCTACCAAGATTT[A/C]AACCCAGAGGAAATG | 83860 |
rs76960858 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | TAF3 | GRCh38.p7 | 10:8008954 | CTCAGTTCTTGAGCT[G/T]CCTCTAGACGTTGAA | 83860 |
rs76967274 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | TAF3 | GRCh38.p7 | 10:7980871 | AGGTTATTTGTCCTC[C/T]CCATCTTACTGTGTA | 83860 |
rs76972018 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7893837 | TTACATAAATTGATC[C/T]TCTTAATTACCACCT | 83860 |
rs77011306 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954543 | AATGAGTGAATTAGT[C/T]CTAGTTAACACAGAG | 83860 |
rs77024172 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TAF3 | GRCh38.p7 | 10:8005488 | TACCTTATGGGTATA[A/G]CCCATTGGGAATCCT | 83860 |
rs77068362 | snp | A/G | 0.106987 | 0.205054 | intron-variant | TAF3 | GRCh38.p7 | 10:7999435 | GGCTGTTAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 83860 |
rs77079359 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7870218 | CATAAAACTCTGATC[A/C]CAAGTCCATCATTCC | 83860 |
rs77100562 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TAF3 | GRCh38.p7 | 10:7913651 | TGTCTAAGTCATGCA[A/G]TGTGGTCGCTGTGCC | 83860 |
rs77121524 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7934389 | ATGTGGTAGGCATTC[C/T]GTCCTTATATAAAAA | 83860 |
rs77127143 | snp | C/T | 0.101658 | 0.201233 | intron-variant | TAF3 | GRCh38.p7 | 10:7980008 | ATTTCAGTGATCCTC[C/T]GTGGTTGTAGCATGA | 83860 |
rs77133414 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:8005905 | CTCTAAAATCAGACT[G/T]CCTTGTTTAAATCCT | 83860 |
rs77149767 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7953243 | ATTTGTTAGTTTCAT[A/G]GTCTTAAAAATATTT | 83860 |
rs77174042 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7838082 | TCCCATTTATGGAAG[C/G]AGAAATGGAAGTTTA | 83860 |
rs77174246 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8013420 | TTATAGTTTTTTTTT[A/T]TATGAAAGGGGTTAC | 83860 |
rs77185895 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7863257 | TTGTACTGGGACTGC[A/G]TGGAACCCATAGACC | 83860 |
rs77217181 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816852 | CTTGTTTTGGGGTGA[C/T]ACATGTCGAGGTGTG | 83860 |
rs77217414 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | TAF3 | GRCh38.p7 | 10:8007685 | CAAAAGCTGCCACCC[A/G]TTTACTCAAATTCCT | 83860 |
rs77254498 | snp | C/T | 0.113685 | 0.209567 | intron-variant | TAF3 | GRCh38.p7 | 10:7986671 | CTCAGCATCTTCAAG[C/T]TTGGCTGTCTCCTCC | 83860 |
rs77280165 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7899851 | GGAAATGAATATACA[C/T]GTGCACAGAAAAATA | 83860 |
rs77302548 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954305 | CTCCCTAGTGAGATT[C/T]AGAGTGCACTCCATA | 83860 |
rs77325215 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TAF3 | GRCh38.p7 | 10:7890820 | CCAAGTGATTAGTCT[A/G]TATCAACTCTTTCCA | 83860 |
rs77330844 | snp | C/G | 0.0189856 | 0.0955633 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816710 | CCCTGGCTTTCACTC[C/G]TTCCCCCAAGTCCCA | 83860 |
rs77344408 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7879705 | CACTTTATTCATCTG[A/G]TGGGCCATAGTTATT | 83860 |
rs77376563 | snp | A/G | 0.135484 | 0.22223 | intron-variant | TAF3 | GRCh38.p7 | 10:7966599 | AAGTATCTCTTCATA[A/G]TGCCACCCCAGAGCT | 83860 |
rs77382679 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7912267 | TGGTTTAGTTTTTTT[A/T]TTAAAAAAAAGAAAT | 83860 |
rs77422857 | snp | C/T | 0.000513385 | 0.0160134 | intron-variant | TAF3 | GRCh38.p7 | 10:7824315 | CTTTTCACTTTGTTT[C/T]AGATGGCCGAACAGA | 83860 |
rs77424503 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7996617 | TGACATTTCAATGTC[C/T]TTTTTTTTTGTATTT | 83860 |
rs77426326 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7912257 | TGTAAAATGATGGTT[A/T]AGTTTTTTTATTAAA | 83860 |
rs77445101 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | TAF3 | GRCh38.p7 | 10:7855476 | CATTTGAGATGCTGG[A/C]AGCCATTTCTTCATC | 83860 |
rs77490304 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7993154 | TAGACCTGTTATTTT[C/T]AATCCACACTCCTAC | 83860 |
rs77504791 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | TAF3 | GRCh38.p7 | 10:7953367 | TTAGGGGCAGGAGTA[A/G]CTCTGTCCTGCCCTT | 83860 |
rs77550535 | snp | A/T | 0.120674 | 0.21395 | intron-variant | TAF3 | GRCh38.p7 | 10:7957352 | AGATACTAACTCTGG[A/T]TGTGTGCTGCTATTG | 83860 |
rs77568257 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7970385 | GGGTTTGGTATAGTG[C/G]TTCCTGTTTTACAGT | 83860 |
rs77578181 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | TAF3 | GRCh38.p7 | 10:7996645 | TTTGTTGTGAGGGGG[G/T]TTTTTTTTGTGTTAT | 83860 |
rs77592224 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7855053 | CTAAAAAAATGAATA[C/G]AATGGGATAAAAGGC | 83860 |
rs77661504 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7997195 | CATGGAAGTGGTTGC[A/G]ATAGTTTTTACCTGT | 83860 |
rs77669520 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7927983 | CCCCACTTTTTTTTT[G/T]GGAGTTCTGGATGTT | 83860 |
rs77732990 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:8000160 | TTTGAGACGGGGTCT[C/T]ACTTTGTTGCCCAGG | 83860 |
rs77754962 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7967247 | ATCCCTTGTGTACCT[A/G]GTAAGTTGGCAGCTG | 83860 |
rs77782484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7828287 | TAGTGTTACCATCAC[A/G]TGCTGAGGATCTGAG | 83860 |
rs77783232 | snp | G/T | 0.0748431 | 0.178382 | intron-variant | TAF3 | GRCh38.p7 | 10:7845817 | GTGAATAGCATTGCT[G/T]TCTTGACATTTCAGA | 83860 |
rs77799172 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | TAF3 | GRCh38.p7 | 10:7986773 | ATCCATAACTCACCC[C/G]AAGCAAAGATACCTT | 83860 |
rs77850488 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7962368 | CTCCCACCCTCATCC[A/G]TCCTGCGTGTTCCTG | 83860 |
rs77874855 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7885853 | CTTGCCTTCATGTTA[C/T]TATTTTTGATTACCT | 83860 |
rs77881632 | snp | A/T | 0.142947 | 0.22592 | intron-variant | TAF3 | GRCh38.p7 | 10:7989250 | TATGTGTTGCTTGGA[A/T]CTAGAGGTAGGATAA | 83860 |
rs77894685 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7902591 | TGTTACATCAGGAGG[C/T]GTATAATGTCAGGCT | 83860 |
rs77897276 | in-del | -/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864832 | TTTATCTTTTTTTTT[-/TT]CCTTTTTATGTTTTG | 83860 |
rs77903493 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7927985 | CCACTTTTTTTTTTG[G/T]AGTTCTGGATGTTTG | 83860 |
rs77942600 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7936777 | AGACATGTATCTACC[A/G]TTGCAGTATCATACA | 83860 |
rs77969713 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940115 | TGGAGTCAGAATGAA[G/T]GAGCAGTGGTGTGAA | 83860 |
rs77997691 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7965818 | ACAAAGCCCACAATT[A/G]TATCTGTATTCTGGG | 83860 |
rs78024545 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7881288 | CTTTTAATATACTGT[C/T]TTCCCACCATGTGTC | 83860 |
rs78026233 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7839078 | GTGTGATCGGACTCC[A/T]GCCCACTTGACATGT | 83860 |
rs78057491 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7927604 | CTAATCTACAAAAAT[A/G]ATTGCTCTATATTTT | 83860 |
rs78076286 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7821007 | TATCTTTAGATATTC[A/C]AAATGTCTCCTGAAT | 83860 |
rs78092115 | snp | C/T | 0.400504 | 0.199621 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817732 | CCCAGGACACTCGGC[C/T]TGCGACACCGGTTTA | 83860 |
rs78096303 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7965930 | TGTAATCAAGCCCTC[A/G]ACACACTAGCAGATG | 83860 |
rs78100565 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | TAF3 | GRCh38.p7 | 10:7823319 | GTCAGCACAGCACAC[C/T]ACTTATTTGATGATT | 83860 |
rs78162199 | snp | C/T | 0.10237 | 0.201756 | intron-variant | TAF3 | GRCh38.p7 | 10:7843076 | AAGTGAGGCTCTCCT[C/T]TGCCTTTCCCATGGA | 83860 |
rs78218175 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7865523 | AACAAACAGAAAGTA[C/G]GGGAGCAAGCTGCCT | 83860 |
rs78291691 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7968685 | GATGAGAAACTAAGG[C/T]TTAGAGAGATTAGTA | 83860 |
rs78313733 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7891371 | ATATAGCCACTTTTT[A/T]AAAAAACCTATAAAT | 83860 |
rs78318599 | snp | A/G | 0.030278 | 0.119257 | intron-variant | TAF3 | GRCh38.p7 | 10:7830245 | CTGAAGGAAATTTAA[A/G]CCCTTTCTCCCAGTT | 83860 |
rs78323520 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7825670 | CCTGTGTCGGGATTT[C/T]GTTGTGTGTTTCGTT | 83860 |
rs78326363 | snp | A/G | 0.207864 | 0.246424 | intron-variant | TAF3 | GRCh38.p7 | 10:7864690 | GAAAGTTCTTTACCT[A/G]TCCTGGTCATCAGTT | 83860 |
rs78343095 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7949091 | CATTACTTTTTTATC[A/G]ACTGCTCTTGATGAT | 83860 |
rs78348394 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | TAF3 | GRCh38.p7 | 10:7987614 | TATTATGCCAAATTA[A/T]CTTCTAAAAGGCTAT | 83860 |
rs78398847 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TAF3 | GRCh38.p7 | 10:7986338 | AGCAGCACCTCAAAA[A/G]TAGCATTTCCAAAAC | 83860 |
rs78414350 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7914307 | AAATGGTTGGTTTCT[A/C]ATCCTTCAAGTATTG | 83860 |
rs78444561 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7947829 | ATCTGATTTGGGATT[C/T]GGAGTTGGAGAGTCA | 83860 |
rs78515857 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | TAF3 | GRCh38.p7 | 10:7981462 | ATATCTCATAATATA[C/T]TGGATCAGGTGATAT | 83860 |
rs78606601 | snp | G/T | 0.0707826 | 0.174302 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015009 | CCCCTCCTCCACTTC[G/T]CTAATACCAGTGACA | 83860 |
rs78611406 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7895710 | GCACACATTTTTTTC[C/T]ACTAATTGTGTGGCC | 83860 |
rs78679257 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7970539 | AGTCTGCTTTGGTGA[C/T]CTAAGTGACAAATGC | 83860 |
rs78687192 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7918237 | CGTGATGAAGGTTTG[A/G]AGAGAGACGAGAATG | 83860 |
rs78691466 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7955825 | AGGAGAATGTAGGGA[G/T]TGTGGATTATTTGTT | 83860 |
rs78720596 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7884734 | ATCCAGGGCACTAGG[A/G]CTGGTCATTGCTATT | 83860 |
rs78726055 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992563 | TTGAGTAGAGCCCTT[G/T]AGAGTGAGTAAAATT | 83860 |
rs78749084 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848326 | TAGAAGGAAATCATT[C/G]TGGACCAATCAGTAA | 83860 |
rs78758983 | snp | A/G | 0.030665 | 0.119967 | intron-variant | TAF3 | GRCh38.p7 | 10:7848873 | GTTGTCAGGCCTGCC[A/G]AAATGGTATGTAGCC | 83860 |
rs78768241 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7875835 | TTATGGAAAACATTT[C/T]AATTCTGTTTTAATC | 83860 |
rs78785065 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7941629 | GGACATCCTTGCTGC[A/G]CCGATGCCTTCGAGG | 83860 |
rs78786421 | snp | C/G | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7899412 | AGGGACCTGGCGCCT[C/G]TGATCCCCAGACTCC | 83860 |
rs78793329 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7980598 | AGTCTATATTGAAGA[C/T]AAAACCAAAACCTAA | 83860 |
rs78803393 | snp | A/T | 0.110519 | 0.207473 | intron-variant | TAF3 | GRCh38.p7 | 10:7850306 | GCGACGGATAGGACA[A/T]TTCATGATGTCAGTT | 83860 |
rs78804160 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7909775 | ATCTTTATTTGCAGA[A/C]TAGGAATCAACAGAG | 83860 |
rs78822339 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901015 | GTGTGCTTGTGGTGA[A/T]CATCCAAAAATTAGT | 83860 |
rs78837569 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7942082 | TTCAGTTATATCTCA[A/G]GAGGTGACAAGTTGA | 83860 |
rs78839887 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | TAF3 | GRCh38.p7 | 10:7828102 | AAGCTGCATTCAGTG[A/G]CACACCCATAGTCCT | 83860 |
rs78854498 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991927 | TTCAAGTTCACTGCA[C/T]ATCATCTTATTACCT | 83860 |
rs78867053 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7996616 | GTGACATTTCAATGT[C/T]TTTTTTTTTTGTATT | 83860 |
rs78872128 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7924383 | TTTTGTTCTGTAATG[C/T]AGCTGTTTTGACTTA | 83860 |
rs78873507 | snp | C/G | 0.0189856 | 0.0955633 | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817366 | AGAACCATAATTTCA[C/G]TTCTATTATTGAGTT | 83860 |
rs78914278 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7896318 | ATTCTTGCCAGAACC[A/G]TTTTCATTCTGGGGA | 83860 |
rs78936154 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7840526 | AGGCATCCAGAATGA[A/G]AAAAAAAAAAAAGAT | 83860 |
rs78939432 | in-del | -/GTT/TTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838367 | AGTTTTGTTTTTTTT[-/GTT/TTG]TGTTGTTGTTGTTTG | 83860 |
rs78983248 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7860374 | GTATGATAGGAGCAT[A/C]TGATCTATGAGAGAA | 83860 |
rs78984256 | snp | A/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7887233 | CCAGACTCTGTATTT[A/T]AAAAAAAAAAAAAAA | 83860 |
rs79016748 | in-del | -/AAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837355 | GCAAAAAAAAAAAAA[-/AAA]GTCAGCTGGGTGTGG | 83860 |
rs79049399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988626 | TATAATGGTGTGCAC[C/T]TGTAGTCCCAGCCAT | 83860 |
rs79064559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833584 | ACCCAGCAATACTGC[C/T]GATTTATTACAAGTC | 83860 |
rs79099540 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | TAF3 | GRCh38.p7 | 10:8002555 | TACTGATAGAGCAGG[A/G]GTAACAAATCTGTGT | 83860 |
rs79117021 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7878522 | GTTCAGCTTGTGGAA[A/G]GTCATCAGGCCACAC | 83860 |
rs79132166 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | TAF3 | GRCh38.p7 | 10:7869863 | TATATTTATGTTTAT[A/G]AACTATTTGTACTTT | 83860 |
rs79155995 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7821343 | TGGAATCTTGTATTC[C/T]ACCCCTTTAAATCCT | 83860 |
rs79159755 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | TAF3 | GRCh38.p7 | 10:7888947 | TCTTGAGAGATTAGC[C/T]CGTGATTGCAGCATA | 83860 |
rs79179290 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7840866 | TTTCTTTTTTTTTTT[G/T]GAGATGGAGTTTTGC | 83860 |
rs79183105 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7989368 | GCAAACCCAGCAGAT[A/G]CCCTGAGCCTAGACC | 83860 |
rs79191449 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7925109 | TATTAACTAATACTG[G/T]CAACTTAACGAGTTT | 83860 |
rs79233740 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7913905 | AGGAGGAGGGAAACA[A/G]CTTGATCCAGAATGT | 83860 |
rs79242879 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7940311 | CAGATGATTCAGTCT[A/C]AATTTAATTAAATCT | 83860 |
rs79257001 | snp | A/C | 0.0876345 | 0.190099 | intron-variant | TAF3 | GRCh38.p7 | 10:7990894 | CTTGTCATGTCCCTG[A/C]AGCTGAGGCTGGAAA | 83860 |
rs79272456 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7900297 | AAATAGTGTTTTGTA[G/T]CAATTATTGATAAAT | 83860 |
rs79275751 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7981429 | TCCCATCATGCATGG[C/T]CATGTTTTCTCTAAT | 83860 |
rs79276637 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002818 | TTGCAGATTCATCTG[G/T]TTCTTACTGTTCTGT | 83860 |
rs79286424 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TAF3 | GRCh38.p7 | 10:7979706 | GATAAATGAAGTGAA[A/G]TAGATTACATTTTAA | 83860 |
rs79301994 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7829536 | TATTGTCGGATGCCC[C/T]TCTAGTGGAATTTTT | 83860 |
rs79302279 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | TAF3 | GRCh38.p7 | 10:7979586 | TGAAAGCATATTATA[C/T]ATCATGTAAACTTTC | 83860 |
rs79335086 | snp | C/G | 0.0711525 | 0.174681 | intron-variant | TAF3 | GRCh38.p7 | 10:7993927 | AGTCTTCAGTGAAAA[C/G]AGTTGATGGAGTTGA | 83860 |
rs79338737 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7898060 | TGTCTTTGCCTTTTA[C/T]TATTCTTTTCAAAAG | 83860 |
rs79339854 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954342 | TGAGTGAATTAGTTC[C/T]AGTTAACACAGAGCT | 83860 |
rs79365035 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7901439 | TCTGGCAAACATTCA[A/G]TTAACTTTTTAGTGC | 83860 |
rs79376812 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7933645 | TGAAAATGTCCTCAA[C/T]GTTTGCACATGCACA | 83860 |
rs79380349 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7892228 | TCATAAGGACTTGGC[A/T]AGGAAATAGATTATT | 83860 |
rs79380963 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TAF3 | GRCh38.p7 | 10:7976193 | TTTGGCAGCCATTGC[C/T]TTCACCACAAATCCA | 83860 |
rs79396642 | snp | G/T | 0.347032 | 0.230401 | intron-variant | TAF3 | GRCh38.p7 | 10:7842161 | ATATTGTTTTTTTTT[G/T]TTGTTTTTTTTTTTG | 83860 |
rs79402200 | snp | C/T | 0.21875 | 0.248039 | intron-variant | TAF3 | GRCh38.p7 | 10:7928094 | AGGATTAAGAGCTCT[C/T]CCATTTGTGCCTATT | 83860 |
rs79410253 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8010965 | CCACATTGTTCTGGG[A/T]CTGTTTTTTAGTTTC | 83860 |
rs79413090 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991925 | TTTTCAAGTTCACTG[C/G]ATATCATCTTATTAC | 83860 |
rs79422129 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7916413 | TTAGCTATGAAGTTG[A/G]ATAAATATGTCTGTT | 83860 |
rs79425017 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | TAF3 | GRCh38.p7 | 10:7982142 | AAATAATAGTAAATG[G/T]TTTTTATCTCACTTT | 83860 |
rs79484260 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7968775 | GGCTGTCAGATGCTA[C/T]AATTTATGGTCCTCA | 83860 |
rs79498018 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:8002727 | TCTTATTCAAACCTA[C/T]ATCTTTGCTGGTTTT | 83860 |
rs79535041 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954576 | CTCCATAGTGAGATT[G/T]AGAGTGCACTCCATA | 83860 |
rs79547153 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | TAF3 | GRCh38.p7 | 10:7905202 | CCCTACGTTAGAGTT[C/T]GAGACCCCAGAGGTA | 83860 |
rs79562615 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7939812 | AGGAGAGAAAAAAGT[C/G]TGAGAAAACTACAGA | 83860 |
rs79577050 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:8004932 | GACCTTTTATTGTAT[G/T]CTCTTTGCTTCTTAG | 83860 |
rs79577927 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7870679 | CGGCAGAACTCGACA[C/G/T]GCTTCTGAGTTCGCC | 83860 |
rs79591297 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | TAF3 | GRCh38.p7 | 10:7867609 | GGAGACAGGTACTCA[C/G]TCATCCTGTATGGTA | 83860 |
rs79630615 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7827779 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 83860 |
rs79632731 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7888399 | AATTTATAAAAAAAA[A/G]GTTTCTTGAATATTT | 83860 |
rs79654362 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7863423 | TGGGACTGGCCTGGC[C/G]AACATGGTGAAACCC | 83860 |
rs79684362 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7931666 | AAAAGCCCATGTTAT[A/G]TTTTCAAATCTCATT | 83860 |
rs79714477 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7889680 | GTTATTCTTCCCAAG[A/G]AGGAATTAATTATTT | 83860 |
rs79721449 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | TAF3 | GRCh38.p7 | 10:7946163 | CTATTTTAAAACTAC[C/T]GGTGACTTCCTATAC | 83860 |
rs79728189 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7895708 | TTGCACACATTTTTT[C/T]CCACTAATTGTGTGG | 83860 |
rs79729612 | snp | A/C | 0.120326 | 0.21374 | intron-variant | TAF3 | GRCh38.p7 | 10:7970274 | CTGAATAAACTAACT[A/C]GATAGTCAACAGTGT | 83860 |
rs79822457 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7863658 | ATATACACACACACA[C/T]ATATATATACACACA | 83860 |
rs79836956 | snp | A/T | 0.0399052 | 0.1355 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016908 | AATAAAACCAAAGAA[A/T]CATTTTCAGGGGGCT | 83860 |
rs79879668 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7914951 | TTTTTTTTTTTTTTT[G/T]TTTTTTTGAGACAGA | 83860 |
rs79883490 | snp | A/G | 0.208779 | 0.246578 | intron-variant | TAF3 | GRCh38.p7 | 10:7947512 | AAGCTACTGGGAGGC[A/G]AGTTGATTGCAATGT | 83860 |
rs79903256 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | TAF3 | GRCh38.p7 | 10:7891630 | ATGTTTTTGTTAGAA[A/T]CTTTTTTCTTAAGAT | 83860 |
rs79904846 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7928992 | AACTGGAGTCTTGAA[A/G]AGAATATTTATTCTT | 83860 |
rs79905220 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | TAF3 | GRCh38.p7 | 10:7916268 | TTAATGTATGTATTT[A/C]TATTTTTGACCATGT | 83860 |
rs79913420 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7914312 | GTTGGTTTCTCATCC[G/T]TCAAGTATTGGCTTA | 83860 |
rs79928831 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | TAF3 | GRCh38.p7 | 10:7991427 | TTTTATTTCATCTTA[C/T]ATTTTACAGTTACTA | 83860 |
rs79930152 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7834502 | TATTATATATAACTC[A/G]GTTGTTCATTGTTTC | 83860 |
rs79998736 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7906201 | TTTTCCTACTGAAGT[A/T]ATAGTTTCAGTGTCT | 83860 |
rs80000200 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7889242 | ATTGCTAGGGTTTTG[A/T]CTTTGATTCTCTTCT | 83860 |
rs80012467 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7989210 | GTGCCTGTGGAGACA[C/G]GGTGGCTCTGATTGG | 83860 |
rs80044884 | in-del | -/AG | 0.382473 | 0.212016 | intron-variant | TAF3 | GRCh38.p7 | 10:7841650 | AGTCACCCAAGGGAC[-/AG]ATGATAGGAAGGACC | 83860 |
rs80050647 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | TAF3 | GRCh38.p7 | 10:7835925 | TTGCCCCAGCTACCA[C/T]TTTCTTCCCAGGATT | 83860 |
rs80070469 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7940151 | GAAGATGGTAGTACA[G/T]ACCATCAGAATTTTG | 83860 |
rs80078561 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | TAF3 | GRCh38.p7 | 10:7934030 | ATCCCAGAGATGCTC[A/T]TTGAGCACAAAATGC | 83860 |
rs80080874 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | TAF3 | GRCh38.p7 | 10:7976256 | TCTTTTTTCTTTTTT[C/T]TTTTTTTTAAGATGG | 83860 |
rs80096516 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | TAF3 | GRCh38.p7 | 10:7880026 | ACCAGCTTGGGCATA[G/T]GGCAGAACCCTGTCT | 83860 |
rs80104768 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7939324 | CATCAGACTCCTACT[A/G]TGTAGGAAATTGGAG | 83860 |
rs80124917 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7937122 | TCCAAGTTTTGGCAG[C/T]TGAATAAAGCTGCTT | 83860 |
rs80146167 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7941839 | ATGTGTGTCAGCAAC[A/G]GAGGGGAGAGACATC | 83860 |
rs80156325 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7843014 | CATGCTTTGCACCTG[C/T]TAGGGCGTAGTCTGT | 83860 |
rs80201383 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7914257 | AAATAATCTGATGTC[C/T]GAGATTTGTGTTAAA | 83860 |
rs80232189 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | TAF3 | GRCh38.p7 | 10:7989700 | GATTCTGATCTACCA[A/G]TATTTCCCATGCTGA | 83860 |
rs80252939 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7989146 | GAAGTCCCAGAGCAA[A/G]CTCTCAGTGGGCCAG | 83860 |
rs80255650 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7827973 | AAAAATAAAACACAT[G/T]ACAGCGAATATTAGT | 83860 |
rs80272151 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7999398 | CAAGACCCAAAACTA[C/T]GTACCAACCTTAATG | 83860 |
rs80288617 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7827780 | GCGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 83860 |
rs80344605 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7997899 | AAAATTATTTTTACA[A/G]CGATCAATTTAGATT | 83860 |
rs111232608 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865371 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 83860 |
rs111249592 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7838160 | AGCAAAGCTGGATTA[A/G]GGTTTAGTTGACTCC | 83860 |
rs111256238 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7899803 | ATGTTGTAAAAATAA[A/G]CAAAACTGTTTAGTA | 83860 |
rs111260517 | snp | C/G/T | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7907052 | TGGGTGGACAGTGTT[C/G/T]GTAGGGCCACCTGGC | 83860 |
rs111264765 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | TAF3 | GRCh38.p7 | 10:7961908 | AGGCTGGAGTGCAGT[A/G]GCGCAATCATGGCTC | 83860 |
rs111268895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7934000 | GCAGAATGAGTGTCA[A/G]TGGCTTGTAGGAAAA | 83860 |
rs111338770 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7911947 | CACTTAAGTTTAAAG[A/C]CCTTACTTTAAATCA | 83860 |
rs111342960 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7884393 | AAGAGCTCTGCCTCC[A/T]TTTTTTTTTTGAGAT | 83860 |
rs111348605 | snp | A/C/G | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7929559 | TGTGCCACCACACCC[A/C/G]GCTAATTTTTGTGAT | 83860 |
rs111365166 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7926147 | ATGTTACTGGTCTGA[C/G]TGAGAAAGGGTAAAT | 83860 |
rs111369524 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7883576 | TCATCAAACTTTTAC[C/G]TACTAGTTTATCATC | 83860 |
rs111372573 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7970420 | AAAACTGCACAGAAA[G/T]GTCGAGTACCTTGCT | 83860 |
rs111375243 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7963573 | ATCATGTTTGAACGC[C/T]GCATGTTCTCACTCA | 83860 |
rs111383436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984156 | TGATTTTTCCAGAAA[A/G]GGAGTTTTTGACTTC | 83860 |
rs111402119 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7985346 | TACCTTGCCTGCCCC[A/G]GCTGGAACTTCGTTC | 83860 |
rs111432401 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | TAF3 | GRCh38.p7 | 10:7947417 | GCTTATTGCATTTTG[G/T]TGAGGGAGACAAAAA | 83860 |
rs111451726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888305 | CTAACCTTTTCAACA[A/G]TGGTTTCCAGAGTGA | 83860 |
rs111465591 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7945035 | GACTACATAACTGTA[A/G]TTGTAATTTTTTACT | 83860 |
rs111491692 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7953819 | ACACAGAGCTCTCCA[C/T]AGTGAGACTCAAGAG | 83860 |
rs111510888 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | TAF3 | GRCh38.p7 | 10:7934063 | CCTTTCTAACACTCT[C/G/T]GATAGCGTAGAGATT | 83860 |
rs111536556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7941579 | GAGCCACTGCCCTCT[A/G]CTTCGCCACTGCCTC | 83860 |
rs111542269 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880626 | TTTCTTATAAATGCA[C/T]TTATATTCCTAGAAT | 83860 |
rs111549138 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7999278 | CCAAAGACAAGATAC[A/G]AATCTTACTCTTAGG | 83860 |
rs111549253 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7991052 | TGACCTTCTCTTTTC[C/T]TTTTTTTCTCTTTTG | 83860 |
rs111550374 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8007407 | GAAAAAAACAAAGTA[A/C]CAAGAACAATAAACA | 83860 |
rs111567697 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881820 | TAACTTTGGAGGAGT[C/T]GCTTACCTTCTCTGT | 83860 |
rs111580970 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7904763 | TTGGAATAGTTACCA[A/G]CATTTGAAACTTGGG | 83860 |
rs111599913 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836996 | ACTTGGGAGGCCAAG[A/G]CAGGAGGATCGTTTG | 83860 |
rs111601410 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7858830 | TGTGTGTGTGTGTGC[A/G]CGCGCCTGCATGTCA | 83860 |
rs111601718 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7909093 | ACCTCTCCCGTGGAG[G/T]CCTGCCAGGGGCCAT | 83860 |
rs111602957 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7834982 | TCATTTCAAGATAGA[A/G]CATTATAGGTTCATC | 83860 |
rs111612736 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7886450 | ATATGTAACTATTTT[C/T]TTCTTTACACAAAAT | 83860 |
rs111694559 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:8000516 | TAATGCCTGCAATCT[C/T]AGCACTTTGGGAGGC | 83860 |
rs111695744 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7867242 | CCAGCCTGGGCAACA[C/G]AGTGAGACTGTCACA | 83860 |
rs111702884 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7854446 | TGATTTTTGGCTCTT[A/G]AGAAGTTAACATGCT | 83860 |
rs111712029 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | TAF3 | GRCh38.p7 | 10:7988461 | CCTGTTATCCCAGCT[A/G]CTCAGGAGGTTGAGG | 83860 |
rs111741261 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7930409 | TAGTATATAGACTCG[C/T]ACAGCCCTATTTCTA | 83860 |
rs111797974 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7992055 | AAGCATCTTTTACTA[A/G]ATAATTACCCATCCT | 83860 |
rs111802899 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7913104 | TCCGCACACACGCCC[A/G]TGATGTCTCTCTTCC | 83860 |
rs111827447 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7918245 | AGGTTTGAAGAGAGA[C/T]GAGAATGTATGAAAT | 83860 |
rs111847964 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954914 | CTCTCCATAGTGAGA[C/T]TCAGAGTGCACTCCA | 83860 |
rs111862412 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7865032 | GGGAGAAGCTTGGTA[A/G]AAATGCCGGTGGATT | 83860 |
rs111886978 | in-del | -/TAAA | 0.46133 | 0.133566 | intron-variant | TAF3 | GRCh38.p7 | 10:7935275 | GCAAAACTCTGTTTC[-/TAAA]TAAATAAATAAATAA | 83860 |
rs111939138 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7907006 | TTACTTTCTCCCATT[C/T]ATTTTGGGCTGAAAT | 83860 |
rs111940203 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7903984 | ACAGAGAGCAGATCT[A/G]GGTCAGGGTGTCTGA | 83860 |
rs111953923 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7975470 | CTGGGTTAGCTGGTA[A/G]ACAGCTAGTATTGGA | 83860 |
rs111962804 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7871529 | GCTCATTGCAATCTC[C/T]GCCTCCCAGGTTCAA | 83860 |
rs112022728 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7950235 | ATGTCTTTGAAAAGA[C/G]AGTATTACTCTTGAG | 83860 |
rs112028449 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7844655 | TGCTGGGATTACAGG[A/C]ATGAACCACCGTGCC | 83860 |
rs112040644 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7955643 | TTATAGTGTTTCTTT[A/C]AAGGCATTTACTATT | 83860 |
rs112043542 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7970969 | TGTAAATAAACCCAA[A/T]AAAGGGGAGGGAAAT | 83860 |
rs112045703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875206 | CCTCCTCGATATTTT[G/T]TTTCTGTCTCCATAC | 83860 |
rs112064731 | in-del | -/CTT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7955743 | TTTGGTGTGTCAGAC[-/CTT]ATTGCCTTGTTCTGT | 83860 |
rs112086325 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7895455 | TTGAAGACAGACAAT[A/G]CTTTTCTTGAAACCA | 83860 |
rs112107694 | in-del | -/T | 0.0333695 | 0.124785 | intron-variant | TAF3 | GRCh38.p7 | 10:7967398 | CAGCAGTCCCATGCC[-/T]TTTCTACAGCATCTA | 83860 |
rs112120363 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7889746 | TTGTGAAATAGCCTC[A/G]TCTTGTGTCTTGTTT | 83860 |
rs112130428 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7988387 | TTGAAATCAGGAGTT[C/T]GAGACCAGCCTGGCC | 83860 |
rs112135905 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TAF3 | GRCh38.p7 | 10:7864225 | TAGAATTTTTCTGTG[C/T]TCTACCTATTCTTCC | 83860 |
rs112136140 | snp | C/T | 0.114387 | 0.210022 | intron-variant | TAF3 | GRCh38.p7 | 10:7987137 | GACCAGCCTGGGCAA[C/T]GTGACAAGATCCTGT | 83860 |
rs112142417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7837255 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 83860 |
rs112146061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946295 | CTCAGACACAAAACT[C/T]GTTACGCAGTATGGC | 83860 |
rs112147355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7936048 | ATCTAAGAGACACGG[C/T]GGTGTCCTGGACTAG | 83860 |
rs112166037 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7894103 | TCGCCTTTTATATTG[A/T]CTTGCAGTAAGCTCT | 83860 |
rs112200861 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7881315 | TGTCGCAATACTTTA[C/T]TGTATCTTGAGAATC | 83860 |
rs112209422 | in-del | -/A | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7886800 | ACTTGTGTAAGCCTT[-/A]ATTCAGGAAGCAAAA | 83860 |
rs112214594 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954769 | AACACAGAGCTCTCC[A/C]TAGTGAGATTCAGAG | 83860 |
rs112236048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7962188 | GTTTGAGTCCTTGCT[C/T]AAGTCTTATACCCTA | 83860 |
rs112239493 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7930163 | GTGATTGTGGTACTG[C/T]GCTCCAACCTGGCAA | 83860 |
rs112252408 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7880204 | TGATCACTCACTGCT[C/G]TCCAGCCTGGGTGAC | 83860 |
rs112273639 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7873625 | CGAGTTCTCCCCCCC[C/G]CCCCGTCAAAAGGGG | 83860 |
rs112300186 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7837760 | GTCTGGGAGGTTGAG[G/T]CTGAGGCTGCAGTGA | 83860 |
rs112309971 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7988469 | CCCAGCTACTCAGGA[A/G]GTTGAGGCAGGAGAA | 83860 |
rs112348743 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7936466 | ATTTCTATGGATTGG[C/T]ATATCAGAAGAGGGT | 83860 |
rs112368607 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7853430 | TATTGTCTTTTTTAT[C/T]GTCTAGACGTCAGGA | 83860 |
rs112375296 | snp | C/G | 0.301177 | 0.244706 | intron-variant | TAF3 | GRCh38.p7 | 10:7863571 | GCTGAGATCGCCCCA[C/G]TGCACTCCAGCCTGA | 83860 |
rs112376924 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7842409 | AACCAGTCTTCCAGC[A/G]TTGGCCTCCCAAAGT | 83860 |
rs112379547 | snp | A/C | 0.0588605 | 0.161139 | intron-variant | TAF3 | GRCh38.p7 | 10:7923719 | CTGCTTTTAAACACA[A/C]AAAAAAAGGACTCCC | 83860 |
rs112403007 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7920332 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 83860 |
rs112411140 | in-del | -/C | 0.281577 | 0.247998 | intron-variant | TAF3 | GRCh38.p7 | 10:7861797 | TCTTTCTTTTTTTTT[-/C]CTCAATGCTTGGGAG | 83860 |
rs112423092 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7997831 | AGAGAAGCAAAGCAC[C/T]GTCTAGAAGTATGAA | 83860 |
rs112442580 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7857631 | TCATCCTGTTTGTGA[A/G]TTATTTCATGAAAGG | 83860 |
rs112448153 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:8012905 | TCTGTTATTGTAAAC[A/C]CTTTGGAAGTTACCT | 83860 |
rs112454023 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7970913 | TCCAAGTCTTTTCTC[A/G]TCAGCTATTGTAATT | 83860 |
rs112477662 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | TAF3 | GRCh38.p7 | 10:7945578 | GCCAGGCCTGCCCTC[C/G]CACTGCAGCCCCCTA | 83860 |
rs112482528 | in-del | -/ACACACAC | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7974134 | TTCCTTCTGAAACAT[-/ACACACAC]ACACACACACACACA | 83860 |
rs112543489 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954935 | GTGCACTCCATAGGC[A/G]AATGAGTGAATTAGT | 83860 |
rs112556160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7913867 | GCTTATAGGAAACAC[A/G]GCAGATAGAGATTAA | 83860 |
rs112563399 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817679 | TTCTGGCAATACTTG[G/T]ATGGAGCTGGGAGAA | 83860 |
rs112577793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954382 | GAGATTCAGAGTGCA[C/T]TCCATAGGCAAATGA | 83860 |
rs112606136 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7858037 | GACAGCTTACAAAGA[A/G]GTTTGAACGGCCTCA | 83860 |
rs112629085 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954144 | AATTAGTCCCAGTTA[A/G]CACAGAGCTCTCCAT | 83860 |
rs112630087 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7934627 | TTTTTGTATTTTTAG[C/T]AGGGACGGAGTTTCA | 83860 |
rs112637324 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7962961 | CCAAGTAGGCAGGGC[A/G]AGTAACATCGGCTCC | 83860 |
rs112643569 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7938363 | CAGGCTGTTATATTT[C/T]AGTTCAGGGGCAATG | 83860 |
rs112680096 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7920727 | AATAATATGGTTAAA[A/T]CTGAAAAGCTTTTTG | 83860 |
rs112710590 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7867163 | ACTCAGGAGGCTGAG[G/T]CAGGAGAATTGCTTG | 83860 |
rs112815233 | snp | C/T | 0.135484 | 0.22223 | intron-variant | TAF3 | GRCh38.p7 | 10:7994760 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCC | 83860 |
rs112845063 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954951 | AATGAGTGAATTAGT[C/T]CTAGTTAACACGAGC | 83860 |
rs112847912 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7971822 | GAAGAAGCTAAATCC[A/T]TGAAGATTAACAAAA | 83860 |
rs112879903 | snp | G/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954926 | AGATTCAGAGTGCAC[G/T]CCATAGGCGAATGAG | 83860 |
rs112942842 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829170 | TATTTTTTAAAATTT[A/G]AAATAGACTATTTTT | 83860 |
rs112946291 | in-del | -/AG | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7903971 | AGGTATCTGGAAAAC[-/AG]AGAGCAGATCTGGGT | 83860 |
rs112971085 | snp | A/G | 0.029116 | 0.117091 | intron-variant | TAF3 | GRCh38.p7 | 10:8010006 | AGCCCCTGCCTCCCA[A/G]GCTCAAGCGATCCTC | 83860 |
rs112974841 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | TAF3 | GRCh38.p7 | 10:7929839 | AAAAAAAATGTCCAG[C/G]CATGACAAGAAAAGA | 83860 |
rs112991637 | snp | C/T | 0 | 0 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8017067 | ATGAACTGGTGGTCT[C/T]AGTCTCTACTGGGTG | 83860 |
rs113007755 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8004122 | GTGGCATGATCACGG[C/G]CCACTGCAACCTCTG | 83860 |
rs113010247 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7977517 | TTTGCTTTATTTGAC[A/G]TAAAGGATTTTTTTT | 83860 |
rs113027718 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7893257 | ATGTAAAGCCCTAGA[G/T]TCCTGAAAGAAAGCT | 83860 |
rs113032936 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7924449 | TGAAATTCCCTGTGA[C/G]CTTTGCTTGTTAAGT | 83860 |
rs113035824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904719 | GTGTAGTGTGCACAG[C/T]GTTGGCTTTCATGAT | 83860 |
rs113057174 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840402 | TGTGATCCGCCCGCC[C/T]CGGCCTCCCAAAGTG | 83860 |
rs113062403 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7962319 | CACATCACTTCAGTA[A/G]TCCATGTTATTGCTC | 83860 |
rs113069659 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | TAF3 | GRCh38.p7 | 10:7994038 | CCCTCCCCCTCTCTC[C/T]TTCTCTGCTCCCCCT | 83860 |
rs113079573 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975049 | TGCACTCCAGCCTGG[C/G]AACAGAACAAGACTC | 83860 |
rs113085587 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7899359 | TGGGTGGCTGGCTTC[C/T]AGCACACACATTCAG | 83860 |
rs113088891 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819042 | CTGCCGCTCCAAACT[C/G]TAGTCATCCTTCGGG | 83860 |
rs113122405 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7892801 | TTCATTATTTCAATA[C/T]ATTTTCTTTTCTTTT | 83860 |
rs113154159 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954765 | AGTTAACACAGAGCT[C/T]TCCCTAGTGAGATTC | 83860 |
rs113186953 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830718 | GGAACTCCTGACCTC[A/T]AGTGATCCGCCAGCC | 83860 |
rs113190840 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909315 | GTTGGTGTACATGCA[C/T]CCTAGTCAGGAGGTG | 83860 |
rs113210528 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7945587 | GCCCTCGCACTGCAG[C/T]CCCCTACCTCCTCCC | 83860 |
rs113211341 | in-del | -/AATA/AATAAATA | 0.175385 | 0.240797 | intron-variant | TAF3 | GRCh38.p7 | 10:7983844 | CCCTGTCTCTAAAAC[-/AATA/AATAAATA]AATAAATAAATAAAT | 83860 |
rs113243876 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954762 | CCTAGTTAACACAGA[A/G]CTCTCCCTAGTGAGA | 83860 |
rs113277867 | snp | A/C | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7911561 | TTAGGGAATATCCTC[A/C]GCTTTGTTTGATAGA | 83860 |
rs113286773 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7842421 | AGCGTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 83860 |
rs113329426 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7871266 | AGGAAATATTAGTAA[C/T]GATGGCTATTTCATT | 83860 |
rs113368487 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | TAF3 | GRCh38.p7 | 10:7886974 | GGCACGGTGGCTTAC[A/C]CCTGTAATCCCAGCA | 83860 |
rs113371444 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7958749 | TCATAACTTCCACGC[A/G]CGTTACTTATTCCTG | 83860 |
rs113376582 | in-del | -/CACA | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7959139 | AACGAGATTCTGTCT[-/CACA]CACACACACACACAC | 83860 |
rs113380182 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7893016 | GTAGAGATGGGGTTT[C/T]TCCATGTTGATCAGG | 83860 |
rs113400752 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7907991 | GTTCAGGAGATACGT[-/AGA]AGAAGTTGGCAGTGG | 83860 |
rs113425826 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7934934 | AAGTCTGTACCGTCA[C/T]GAAGCTTTGTCTGGG | 83860 |
rs113431311 | in-del | -/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7839377 | TTCACCATTTTTTTG[-/G]CAGAAAACCTATGGT | 83860 |
rs113444048 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818958 | TCCCTCCGCGTCCCC[A/G]GGGTGTGCATCCCGC | 83860 |
rs113455164 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7912207 | GTTGAAGCCGTCTGT[A/G]TTAACTAAACCAAAT | 83860 |
rs113455910 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844927 | TTAATATTTTAAAAT[A/G]TTGCAATGTTGCATC | 83860 |
rs113542174 | snp | A/C/T | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7935243 | GATCGTGCCACTGCA[A/C/T]TCCAGCCTGGGCAAC | 83860 |
rs113581865 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TAF3 | GRCh38.p7 | 10:7866862 | TTTGTTTTTATGGTG[C/T]GCTCTAAAAAGTAAT | 83860 |
rs113585857 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7954944 | ATAGGCGAATGAGTG[A/G]ATTAGTTCTAGTTAA | 83860 |
rs113656736 | snp | A/C/G | 0.00557861 | 0.0525638 | intron-variant | TAF3 | GRCh38.p7 | 10:7837504 | AAAAATTAGCTGGGC[A/C/G]TGGTGGTGCGTGCCT | 83860 |
rs113671562 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TAF3 | GRCh38.p7 | 10:8000359 | CAACCTCAGGTGATC[C/T]GCCTGTGTTGGCCTC | 83860 |
rs113687637 | snp | C/T | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009177 | GCCCGCCCCCGGCCC[C/T]ATGCTCGTCAGCCCT | 83860 |
rs113700540 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859452 | TCAGTCCATTCCAGA[C/T]TGGGGGAGAATAGTA | 83860 |
rs113710166 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | TAF3 | GRCh38.p7 | 10:7996633 | TTTTTTTTTGTATTT[A/G]TTGTGAGGGGGGTTT | 83860 |
rs113727803 | snp | C/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7875902 | CATTTTTTTCTTGTA[C/T]GACTAATTTTACCGA | 83860 |
rs113730774 | in-del | -/TTTT | 0 | 0 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817850 | CAGGCAGCTTACCTG[-/TTTT]TTTTAAAAAAAAAAA | 83860 |
rs113741610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7981914 | TTAAAATCAATATGT[A/G]TAGACACTTGTCTTT | 83860 |
rs113745052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7928608 | TAGGATTGCCCTTGT[A/G]TTAATAACCATGAAC | 83860 |
rs113761230 | snp | A/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7887221 | TGGGTGACAGAGCCA[A/G]ACTCTGTATTTAAAA | 83860 |
rs113789347 | in-del | -/T/TT | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7996842 | CACCACCACACTCTA[-/T/TT]ATTTTTTTTTTTTTT | 83860 |
rs113808455 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7898076 | TATTCTTTTCAAAAG[C/T]TTTTCTTGATTTTAT | 83860 |
rs113811177 | snp | A/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7870000 | TGCATATTTAAATTT[A/T]TTTTTAGGGATTTCA | 83860 |
rs113817768 | snp | C/G | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7939634 | CACCTCTACCTACAC[C/G]CCTTCCAAGAGACAA | 83860 |
rs113818169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904377 | GAAATGATCTTTGAT[A/G]TATTTTTTTCTTTAA | 83860 |
rs113820359 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7929757 | AAATAAGAATATGGA[A/G]TACTCTTTCTGCTCA | 83860 |
rs113820985 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841053 | AGGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 83860 |
rs113827773 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7984734 | AGTGAATATAGGAAA[A/G]TACTTAAGATTCATT | 83860 |
rs113834188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7846253 | TGAGCCACTGCGCCC[A/G]GCCAAAAGGATGAAG | 83860 |
rs113837510 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7957524 | TTAATTTTCAGAATA[A/C]TCTCAAGATAAATGG | 83860 |
rs113876058 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7961889 | GGGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 83860 |
rs113936432 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7940830 | AGCTGGGTATGATGG[C/T]GCATGGCTGTTCCAG | 83860 |
rs113948596 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7897539 | TTTTTTTCATGGTAC[C/T]GCTAAGGCAACTGAT | 83860 |
rs113952777 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7886826 | CAAAACTTATGCTTA[A/C]AAAATTAATAGAAAA | 83860 |
rs113953134 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7940876 | AGGTAAGAGGATCAC[C/T]TGGACCCAGGAGTTT | 83860 |
rs113989248 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | TAF3 | GRCh38.p7 | 10:7938263 | CTAGGGATGGGGAGG[G/T]GTGTGGGGATAAGAA | 83860 |
rs113995184 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7842940 | AACGCTTACAGTACA[A/G]TAAATATATGCATTT | 83860 |
rs113998208 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7835204 | CACTAACACCATCGA[C/T]AGCTGCTGAGCTAGA | 83860 |
rs114035653 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7856744 | TGGAACATTTTGTTA[C/T]ACCAAGTAGCAAGGA | 83860 |
rs114039722 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7928297 | ATACCTAGTGCCACA[C/T]AGGAAGTACTTAAGT | 83860 |
rs114053941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7843138 | TGAATATGTTCTTGA[A/G]ACAGGGTCTTTCCCT | 83860 |
rs114054696 | snp | A/G | 0.300421 | 0.244863 | intron-variant | TAF3 | GRCh38.p7 | 10:7824306 | TTTGATTTGCTTTTC[A/G]CTTTGTTTCAGATGG | 83860 |
rs114067582 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | TAF3 | GRCh38.p7 | 10:7829486 | TTTTCTTGTTTTTGA[C/T]GACCTTGACAGTTTT | 83860 |
rs114102784 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | TAF3 | GRCh38.p7 | 10:8008020 | GCTCTAGCGACCTGC[A/G]GCAGCATCACCAGGA | 83860 |
rs114112198 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | TAF3 | GRCh38.p7 | 10:7831954 | GGGGGTGCAAAGCGA[C/T]GTTATGTTTTATAAA | 83860 |
rs114117798 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7890292 | TTCATTTCAGATTCT[C/T]CTTAGCCTCTCCCAG | 83860 |
rs114122170 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TAF3 | GRCh38.p7 | 10:7870303 | GTATATTAGAAACCA[A/G]TTCTCACTTTTCCGG | 83860 |
rs114128996 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7983791 | CTACAGTGAGCTGTC[A/G]TTGCACTGCTGCACT | 83860 |
rs114129893 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7957671 | CATATGTACAGAAGA[A/G]TCCTTTTCTCCCGTT | 83860 |
rs114132750 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7929078 | GGTTTGGTTTTTAAG[A/G]GAGGTTTTTGCCTTC | 83860 |
rs114139221 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7906377 | GACAAAGCTATCAGA[A/C]ACAGGTGGTAACTAC | 83860 |
rs114141153 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7996389 | ATCCTTGGAGGTGAC[A/G]TGGTTATTTTCACCA | 83860 |
rs114188237 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7936232 | CAGTAACAATATTTT[C/T]CTGAAGTAAAACAAT | 83860 |
rs114193368 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838924 | TTTTTTTTTTTTTTT[G/T]GTTTGTTTGTTTTGT | 83860 |
rs114195153 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7855445 | ACACCGGATGCCGAG[A/G]TGTCCAGCCTCCTTC | 83860 |
rs114281683 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7876310 | TACCTGAAAGCAATA[C/T]TTTAGCTTCACATTT | 83860 |
rs114282714 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7917655 | TCGGGTTCTGAGGCC[A/G]TCACCGGTTGGGGGA | 83860 |
rs114389179 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | TAF3 | GRCh38.p7 | 10:8004691 | TTCTTTTTTCCCTCT[A/G]GCTGCCTTTCAGATT | 83860 |
rs114422773 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7967415 | TTCTACAGCATCTAC[C/T]TGACTTTAGGGAAGA | 83860 |
rs114441575 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | TAF3 | GRCh38.p7 | 10:7832974 | TCTGAGGCAGGAGGA[G/T]GATTTGAGGCCAGGA | 83860 |
rs114465128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926199 | ATGACCTAAATAATC[A/G]TATGATATTTTCCTC | 83860 |
rs114472434 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7872455 | AGGAAGTTATATTGC[C/T]GTTTATCAGCACTAA | 83860 |
rs114482528 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TAF3 | GRCh38.p7 | 10:7866463 | ATGAGAGCCAGTCAT[C/T]GTGACCAGCAAAGAA | 83860 |
rs114495065 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7939087 | TCCAAGAGTTCAGAA[A/G]CAGGGGTCATCAGGA | 83860 |
rs114505538 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7827971 | AAAAAAATAAAACAC[A/C]TGACAGCGAATATTA | 83860 |
rs114541691 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | TAF3 | GRCh38.p7 | 10:7970434 | AGGTCGAGTACCTTG[A/C]TGTAGCCAGTGAGGG | 83860 |
rs114551005 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7986513 | TTTCTTTATGTCATA[A/G]TGTCAGACTGGGTGT | 83860 |
rs114571316 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7847744 | GCTACCATGCCTGGT[A/C]TGTTTAGATTCTTGT | 83860 |
rs114580542 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7932824 | CTGGTAATACAGATA[G/T]GCACTACCACACCGA | 83860 |
rs114581772 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7928308 | CACATAGGAAGTACT[G/T]AAGTATTTTTTGAGT | 83860 |
rs114590066 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7919253 | TCTTGATTATCTCCT[A/C]GGGGAAAGTGATACT | 83860 |
rs114618073 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7928688 | TTCTATTCCTTCTGG[G/T]GTTGTCTGTCATTCT | 83860 |
rs114624877 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:7865040 | CTTGGTAGAAATGCC[A/G]GTGGATTTGTGGATA | 83860 |
rs114635053 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7907432 | TTTATATTAGAAAAA[C/T]ACAATTAGCCCAAGG | 83860 |
rs114647041 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7948330 | CCAGCTTCAAGCAGT[C/T]CTCCTGCCTCAGCCT | 83860 |
rs114685248 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:7946316 | GCAGTATGGCTGTCC[A/C]CATGCTGTCCCTGCA | 83860 |
rs114739466 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:8008963 | TGAGCTGCCTCTAGA[C/T]GTTGAAGTATTTCGC | 83860 |
rs114768308 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7838853 | AGGCTGGAGTTCCAG[A/G]GTCTGGGGAACGTTC | 83860 |
rs114789254 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7905056 | GGAAAAACCAAAGAT[A/G]GACTGAAAGGCTCCA | 83860 |
rs114832759 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7853741 | TGCTTTGGCACTACA[A/G]TGGCGGAGATGAGAT | 83860 |
rs114872435 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7888441 | TTCATTTACTTTTGA[C/T]ACATTTAAACATTGA | 83860 |
rs114900301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006834 | GCCGTGAACATGGCA[C/T]GGGGCCGGCAGTTCC | 83860 |
rs114912883 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7887988 | GAATTCATATTTAAA[A/G]TGCCCCTGCCACCAC | 83860 |
rs114962653 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7851103 | GTATGTTTGGAAGAG[A/G]ATAAGTACTATGAGA | 83860 |
rs114964150 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7903425 | TCAGCCTTGGAAGCA[A/G]CTCTTTCTCCAGGAA | 83860 |
rs114969674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987255 | TGGGAAATCGAGGCT[A/G]CAGTGAGTCGTGATC | 83860 |
rs114982241 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7823108 | GCAGAGTGAGACCCT[C/G]TCTCAAAAAACGAAC | 83860 |
rs114991998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7972099 | CCCTTAAAAGCTCAT[C/T]GTGGCCCCAGATTTT | 83860 |
rs115010038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7932365 | GGGAATGGCATCTCA[A/G]CTAGCTAGTGTTCCA | 83860 |
rs115013134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968501 | ACAAGTTTTTTAGCT[G/T]CTTTAATCCTTAAGT | 83860 |
rs115032636 | snp | A/C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7894254 | CAAATTCTCCCATGA[A/C/T]GGAGTTACTGTCAGC | 83860 |
rs115088035 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7893572 | GCTTTTGTTGCTGTA[C/G]CTAGTTGCTCCACCT | 83860 |
rs115092760 | snp | A/G | 0.046775 | 0.145601 | intron-variant | TAF3 | GRCh38.p7 | 10:7983712 | GACGTAGTGGCGTGC[A/G]CCTATACTCCCAGCT | 83860 |
rs115095904 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7957046 | ATAACACATAATTTT[C/T]AATACATTCTCACAC | 83860 |
rs115096820 | snp | A/C | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7910023 | AATATAACATAAATG[A/C]TATGTAAATAGTTGT | 83860 |
rs115097774 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7928713 | CATTCTACTCACGAT[G/T]ATCTAGGTAATGGCC | 83860 |
rs115163816 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7990825 | TCCTGCTCTGAGCCC[G/T]TATCCCATAGACCTC | 83860 |
rs115167320 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7905211 | AGAGTTTGAGACCCC[A/G]GAGGTAGACCGTACA | 83860 |
rs115184558 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7895510 | TCATGGTCCTGGCAC[A/G]AACACCTTGGCCTGC | 83860 |
rs115200138 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7920271 | ATAAATAATTTTTTA[A/G]TTTTAAAAATTAAAA | 83860 |
rs115223384 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7985089 | CCCACGCCTGCCTGC[A/G]TAGCTTCTAGAGTGA | 83860 |
rs115258847 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:8004845 | GTTCTGTAAAAGTCT[C/G]AGGTACTCTTTGTTA | 83860 |
rs115277784 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7905942 | TTTATCAAATATATG[A/G]TAAATGCACCAATTT | 83860 |
rs115280206 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7911252 | CTGAGTATTCAAACC[C/G]ATGAGGCATTGTGAT | 83860 |
rs115288446 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | TAF3 | GRCh38.p7 | 10:7980200 | AGGGGGGTATTTATT[G/T]CTGAAGAACAGGCAG | 83860 |
rs115290237 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7951116 | TTATAGGAACCTAAC[C/T]GTGTATTTCTCTTAA | 83860 |
rs115313955 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7847895 | GAGGCTGAGCCTCCC[A/G]AGTAGCTGAGACTAC | 83860 |
rs115329121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7868398 | TGGTGTGACATTAGC[A/G]GTCAAGTCTAGTGAC | 83860 |
rs115346387 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | TAF3 | GRCh38.p7 | 10:7916002 | AAAAAAAAAACCATG[C/T]AGTTTTTAAAGCCCC | 83860 |
rs115355481 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7973958 | CATGGTGAAACCCTG[A/T]CTCTAATACAAATAC | 83860 |
rs115376823 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7842366 | GGTTTCAGTATATTG[C/T]CCTGGCTGGTCTTGA | 83860 |
rs115389464 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7908761 | AGGGAAACCTGATAT[C/G]TAAGACAGATTAGTT | 83860 |
rs115419206 | snp | A/C | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7967341 | TGGAGTTGTTTCAAC[A/C]GCCATTATGAATTTG | 83860 |
rs115483394 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820064 | TGCCATGCTAATCTG[C/T]GACCACGCTGAGCTA | 83860 |
rs115514025 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7919341 | GTGGACAGTATTGAG[C/G]CCGGGGAGGGATGGT | 83860 |
rs115522160 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:8012501 | GGCACACAGAGTCAC[A/G]GCCTTCTGACTTCAA | 83860 |
rs115531244 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7951473 | CCTGGGCTCATTCCT[G/T]TGGCAGTGGTTGCAG | 83860 |
rs115546624 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7869738 | ACCCCTGCAGCAGCA[C/T]GGACTGCCTCCTTCC | 83860 |
rs115546829 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8002572 | TAACAAATCTGTGTA[C/G]AAACTATTCAAATTG | 83860 |
rs115550816 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7912992 | GGAGAATGGGAGTCT[A/G]GGACCGAGGGGTCAG | 83860 |
rs115551434 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7844352 | TCTCTCATTCTGACA[C/T]AGCAGCTTTTCTTCT | 83860 |
rs115555120 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TAF3 | GRCh38.p7 | 10:7868190 | ATTGTTTGACAAGCG[A/G]GATGTTCTGAAATAA | 83860 |
rs115555285 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7908404 | TAATCAAAATCTCCT[A/C]AACTTTAAGCATTGG | 83860 |
rs115555668 | snp | A/C | 0.0752113 | 0.178743 | intron-variant | TAF3 | GRCh38.p7 | 10:7849671 | TTGGGGGGGTTCATG[A/C]GAACTTTTTTTTTTT | 83860 |
rs115560733 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | TAF3 | GRCh38.p7 | 10:7912804 | TCTGTGGCTGTAGAA[A/G]CGCTGTTTGGCGAGG | 83860 |
rs115597598 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TAF3 | GRCh38.p7 | 10:7953921 | ACTCCATAGGTGAAT[A/G]AGCGGATTAGTCCTA | 83860 |
rs115616699 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7856051 | AGGAAATGGGGGAAA[A/T]GAAGAAGGGGAAGCC | 83860 |
rs115619089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7960896 | TAATAAAGAACAGCC[A/G]TTTCTACTGTGCAGT | 83860 |
rs115675563 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7976801 | ATTTCAACTTTCTCA[C/T]TTGATAACGCAAACT | 83860 |
rs115719838 | snp | A/T | 0.0755793 | 0.179102 | intron-variant | TAF3 | GRCh38.p7 | 10:7863287 | CAATTTGGAGAGAGT[A/T]GAGATCTTCACAATA | 83860 |
rs115744059 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7947661 | GAAGCTTGGTGAGTT[G/T]GAGAAGCATCGAAGA | 83860 |
rs115746542 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7838088 | TTATGGAAGGAGAAA[G/T]GGAAGTTTAAAAATC | 83860 |
rs115779339 | snp | A/T | 0.029116 | 0.117091 | intron-variant | TAF3 | GRCh38.p7 | 10:7929457 | ACTAGGCTGGAGTGC[A/T]CCTGATCTTGGCTCA | 83860 |
rs115789652 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7914553 | GACCTGTGGCAGGTT[C/T]TCAGTAAATGCATCT | 83860 |
rs115792039 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7965851 | TAAATCACCCATCAC[A/T]TAAGTGGAAATATGT | 83860 |
rs115827152 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7960252 | GATTTTCTCATGTTT[A/G]TCTGTTGGCAGTTGA | 83860 |
rs115846727 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7907440 | AGAAAAATACAATTA[G/T]CCCAAGGATCCAGTG | 83860 |
rs115850251 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7930414 | TATAGACTCGTACAG[C/G]CCTATTTCTAGAGTA | 83860 |
rs115853888 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7998562 | TGTAGGAAACATAGG[A/G]AGAGGTGGGGCATGG | 83860 |
rs115890127 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7966464 | GCAGTTTTGTAGGCA[C/T]TGGGGCCTCAGTCCT | 83860 |
rs115890604 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:8004009 | GTTACTTTTAAATGA[A/G]TTACTAAATATTTTT | 83860 |
rs115891726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7909313 | CTGTTGGTGTACATG[C/T]ACCCTAGTCAGGAGG | 83860 |
rs115907076 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7835371 | AGGGTAGCTCCTCTG[A/G]CTTTGCAGTGCTCCC | 83860 |
rs115913299 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7847197 | TTACAACATCCTAGA[A/G]GAATTATAAGAAAAT | 83860 |
rs115924056 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7918703 | CTTAGCTAGGTTTTG[G/T]ATGTATTATATTCCG | 83860 |
rs115949976 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7892400 | AGAAAGAACCATAAT[A/G]TACTTTTCTTTGTTC | 83860 |
rs115951834 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7899852 | GAAATGAATATACAC[G/T]TGCACAGAAAAATAC | 83860 |
rs115968383 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7987153 | GTGACAAGATCCTGT[C/G]TCTACAAAAAATAGA | 83860 |
rs115969386 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7922917 | ACAAATAATAGGCTT[A/G]TTAGAAAACTTGTAT | 83860 |
rs115997760 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7982820 | TGGTGTCCTCCACAG[C/T]GGTTTTTATAGGTGA | 83860 |
rs116001889 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7946950 | GTTTGTTTTTGGAGG[C/T]GGATTCTCGCTACAC | 83860 |
rs116008269 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7909079 | TCGCTGGGCCTGTCA[C/T]CTCTCCCGTGGAGGC | 83860 |
rs116017319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8000804 | TAAATAGATAAAACA[C/T]CTATAATTTTCATGT | 83860 |
rs116023832 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7892210 | TATGCTCTTTTGTCT[A/G]TTTCATAAGGACTTG | 83860 |
rs116026060 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7912552 | TCTGTAAAAGTAAGA[C/G]TGAAAAGCAAGACCT | 83860 |
rs116027816 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TAF3 | GRCh38.p7 | 10:7904700 | AGGTGGGTGGGCTGG[A/G]ACTGTGTAGTGTGCA | 83860 |
rs116030713 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7820653 | GGATACGCCACCATG[C/G]CTGGCTAATCTTTTT | 83860 |
rs116085466 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TAF3 | GRCh38.p7 | 10:8006051 | AAAAACAAACAAGGC[C/T]GGGCACCGTGGCTTA | 83860 |
rs116117178 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:8002292 | TTTTCATTGATATCC[C/T]GTATTTCTCTCACCT | 83860 |
rs116132486 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7870688 | TCGACACGCTTCTGA[A/G]TTCGCCTTCCTTCAC | 83860 |
rs116151048 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7924532 | CATTTGCACATCTTT[A/G]TGTGGGCATGTCTCC | 83860 |
rs116158436 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7985196 | CATGTGGAACTGCCT[C/T]GCCATGTTACCCCAG | 83860 |
rs116159800 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | TAF3 | GRCh38.p7 | 10:7978995 | GCAGTGAGCTATGAT[C/T]GTGCCCACTGCACTC | 83860 |
rs116177008 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7990727 | ATTCCCCATCAGTTC[A/C]AAGGTCTCTGTAGGG | 83860 |
rs116184764 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7905609 | AAGCAGGGCCAGGCG[C/T]GGTGGCTCACACCTG | 83860 |
rs116246992 | snp | A/G | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819111 | GGGAGTCGGGTCTTC[A/G]CTCCCAGCTCCACAC | 83860 |
rs116265053 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7998934 | TATTCATTATGTGTT[C/T]GGTATAGCTGAAAAC | 83860 |
rs116295636 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7959307 | AAGAAACCTTTGTTT[A/G]TTCTAAAAAAAATCT | 83860 |
rs116305342 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7966669 | TTGAGCTTGGCCACA[A/G]AATAATACCCAGTAG | 83860 |
rs116306249 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7921862 | TTTTCTAATTCTGAC[A/G]TTGTCATATGATCAA | 83860 |
rs116322044 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7940206 | TCTATTTTCAACCAC[A/G]CTGTTAGGTCAGAGG | 83860 |
rs116333585 | snp | C/G | 0.021333 | 0.101051 | intron-variant | TAF3 | GRCh38.p7 | 10:7861614 | TTTTAGCACTTTACA[C/G]ATATTTTTCCACCAT | 83860 |
rs116394140 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7881724 | ATTCAGCTGGTAGAA[A/G]TGATGTGTAGCAGAA | 83860 |
rs116414320 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7856750 | ATTTTGTTATACCAA[A/G]TAGCAAGGAAGCTAC | 83860 |
rs116417641 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7943560 | GCCTGAGAGCCACCA[A/G]ACTTGCACACTGCTA | 83860 |
rs116433580 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TAF3 | GRCh38.p7 | 10:8009659 | AGAGTTTCGCTCTTA[C/T]TGCCCAACCTGGAAT | 83860 |
rs116433849 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:8003993 | TAATGGGTTCATTGT[C/T]GTTACTTTTAAATGA | 83860 |
rs116443040 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7911602 | TGGCAGCAGCAGGAC[A/G]TTTACCAGAGGTTGC | 83860 |
rs116445988 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | TAF3 | GRCh38.p7 | 10:7958507 | TAAAAAAAAAAATTA[G/T]AGTATCATACTATTT | 83860 |
rs116447385 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7950271 | AAGGGAGAGAGATAG[A/G]GAAATATAGAACGAC | 83860 |
rs116449312 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7870498 | TTTCTGGTGGTTCAT[C/T]ATAAAATACATTTTT | 83860 |
rs116476268 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7884706 | CTCCTTTTTTTGAAG[A/G]ATAGAGTCTAGAATC | 83860 |
rs116530973 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7873696 | GGGTACGTCATAAAG[A/C]AGATGGGACCAGGTA | 83860 |
rs116561853 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7980574 | TAATGGGTGTCCAGA[A/G]TTCCCTGTAGTCTAT | 83860 |
rs116607642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967850 | TGGGCAGGTCAGCTA[A/T]TAATAGGTTTTAAAA | 83860 |
rs116638783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8007658 | AGCTTTGGAATCAAG[C/T]AGACTTTGGTTCAAA | 83860 |
rs116640812 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7888462 | TAAACATTGACACCC[C/G]TTAATTAGTAATAGG | 83860 |
rs116647697 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7935767 | TCCAAAGAGAGGAAG[C/T]GCAGATTCCAGGCCT | 83860 |
rs116669303 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7866380 | TAGGGGCCTGTGATG[A/G]TGGCTGACCACGGAA | 83860 |
rs116669985 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | TAF3 | GRCh38.p7 | 10:7873278 | CTAAAAAGTTGGCTC[C/T]GTTGAAATTGTGTTT | 83860 |
rs116701709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7909310 | GAACTGTTGGTGTAC[A/G]TGCACCCTAGTCAGG | 83860 |
rs116703109 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | TAF3 | GRCh38.p7 | 10:7969855 | CAGCTCTGCCACTTA[C/G]TCGTTATTCACCAAC | 83860 |
rs116705062 | snp | A/C/G | 0.031825 | 0.122064 | intron-variant | TAF3 | GRCh38.p7 | 10:7919205 | GCCTAGCTTCTGGCT[A/C/G]AGGTAATGGGGGATG | 83860 |
rs116719446 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7993130 | TATATCTCATAAGGA[C/T]TTGTAATCTAGACCT | 83860 |
rs116720620 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TAF3 | GRCh38.p7 | 10:7986097 | CCTTTCATTCTCTCT[C/T]ACCATGGATTCCTTT | 83860 |
rs116721998 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | TAF3 | GRCh38.p7 | 10:7848331 | GGAAATCATTCTGGA[C/T]CAATCAGTAATGGAA | 83860 |
rs116738893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820118 | AGCTGTCCATTCCTA[C/T]ATGCGTGCTGTTTCT | 83860 |
rs116738943 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7822583 | GCAGCTTCCACCCCT[C/T]GAACTGTTAACCATT | 83860 |
rs116752145 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7875419 | GTGATAATTTTTCCT[C/T]AACATTAGGTCAATT | 83860 |
rs116759342 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | TAF3 | GRCh38.p7 | 10:7960708 | GGGAGCACCTTGTCA[C/G]TCATACTGGAGAAAT | 83860 |
rs116760061 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7832448 | ATAAATATTTATGGA[A/G]TACATAAGAATTTTA | 83860 |
rs116762519 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7869164 | GAAAAATTTTAAAAT[G/T]TAGATAAAAAATGTT | 83860 |
rs116776043 | snp | C/G/T | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7974313 | ATCAGCCAAGAGTGA[C/G/T]GTTGGCTAGGGGGAA | 83860 |
rs116788983 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7882013 | GCAGTTAAACAGGTG[A/T]CGATTGGGCACCTAC | 83860 |
rs116793455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7889180 | CATGACAGTACTGTT[C/T]CTTCTTCTGCTCCAG | 83860 |
rs116851163 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7874121 | GCTGTGAGCTTGTCA[C/T]ATAAAATATACCTCT | 83860 |
rs116877691 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7980870 | CAGGTTATTTGTCCT[C/T]CCCATCTTACTGTGT | 83860 |
rs116947071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896510 | TTGCTTCATAGATCT[C/G]TAGTTGCCATAGCCC | 83860 |
rs116962060 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | TAF3 | GRCh38.p7 | 10:7999587 | CCAGCATCTCAAGTA[G/T]CTGGGATTATAAGTG | 83860 |
rs116979108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7934131 | GGTTGAAAAATCATT[C/T]GGAAGAATTAGAAAC | 83860 |
rs117017793 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7836050 | TATGATGAGCTCCAT[C/T]TTGGGGCCTTTCTTG | 83860 |
rs117028921 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7918855 | AGATGTTTACTGCAA[A/G]GAGGGATAGCAGGTG | 83860 |
rs117082144 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7958550 | AAAACAAGCAAACTA[C/T]CTACAAATATGGTAA | 83860 |
rs117105571 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7989172 | GCCAGCTGAGATCAC[A/G]TGACCAGCCTGAACC | 83860 |
rs117128113 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | TAF3 | GRCh38.p7 | 10:7865114 | GGGAAGCTTCAGAGG[C/G]AAGTGAGTGGGGCCT | 83860 |
rs117147712 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | TAF3 | GRCh38.p7 | 10:7833996 | AGGACAACAGCCAGA[A/C]TGTTCTTTCTATAGA | 83860 |
rs117149489 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | TAF3 | GRCh38.p7 | 10:7837728 | TACTCAGAGGCTGAG[A/G]TAGGGGGATCACTTG | 83860 |
rs117156198 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7985461 | TCACCTTCATCAAGC[C/T]TTCCCTCTGTATGAG | 83860 |
rs117180094 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7886356 | AACCCCCTTCTGCAT[A/G]TTCTTCATTTTCTTT | 83860 |
rs117251400 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819021 | TCCCACGTCCCTGGG[C/T]TTCCACTGCCGCTCC | 83860 |
rs117270373 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7923920 | GAACTGTTGAATTTC[G/T]ATTTGGAAATAAAGG | 83860 |
rs117301282 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7874313 | TTTTTAAAGAAATGC[A/G]AAAGGACAGCTAGTA | 83860 |
rs117372750 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7989854 | GCCAAAGTTTGGAGC[A/G]TAATGTTCCTGGTAT | 83860 |
rs117376494 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7899691 | GTTCACAGTAAACAT[A/G]TTACTAAATAAAATG | 83860 |
rs117393960 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:8009406 | GCTCTGAATCACTAT[C/T]GAATTTCAGACGCAT | 83860 |
rs117489619 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7909066 | CCCTTACCAGCCGTC[A/G]CTGGGCCTGTCACCT | 83860 |
rs117494206 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7910010 | GTTACTTATAATTAA[C/T]ATAACATAAATGCTA | 83860 |
rs117503332 | snp | C/T | 0.00386878 | 0.0438112 | missense | TAF3 | GRCh38.p7 | 10:7977260 | AAGTGGAACCAGTCG[C/T]TCTGGCCCCGAGTCC | 83860 |
rs117529430 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:8011042 | GTTCTTTGGATACTA[C/T]AGAATTAAACACACA | 83860 |
rs117549156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8001836 | TCTCAATTGCACATG[C/T]GTAATTATTGCATAG | 83860 |
rs117565981 | snp | A/G | 0.0326508 | 0.123529 | intron-variant | TAF3 | GRCh38.p7 | 10:7977336 | GATGTAAGTATAAAC[A/G]TTTTGAATCAGGGTG | 83860 |
rs117608276 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7834174 | TTCACTCTGCTGTTT[C/G]CTTTATTGTGCCAAA | 83860 |
rs117614268 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7909812 | GTTGAGCCTATAACA[G/T]TGAAACCTTTATTCT | 83860 |
rs117633221 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7938186 | GCATCCCTGCCTAAA[G/T]ATTCATGGAGTTTAA | 83860 |
rs117638531 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7898157 | ATATGGAAGTACAAA[A/T]GGCTTCAACAGTAAT | 83860 |
rs117668067 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TAF3 | GRCh38.p7 | 10:7838032 | TTATCTCATTTAATC[C/T]TGAAACAGGTCCTAA | 83860 |
rs117672782 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7925283 | TGGACATGTGTGTGG[A/C]CCCTCTGGCAGGTCA | 83860 |
rs117701308 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7987285 | CATGCCACTGCACAC[C/T]AGCTTGGGCAATAGG | 83860 |
rs117701383 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7920110 | AAATAAAAATTAGCC[A/G]GGCATGTTGGCATGT | 83860 |
rs117733404 | snp | A/G | 9.97059e-05 | 0.00705996 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964668 | GGTAGCAGATAAAAC[A/G]ATTGAGGCCTCTATC | 83860 |
rs117805016 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | TAF3 | GRCh38.p7 | 10:7914253 | GGTGAAATAATCTGA[C/T]GTCCGAGATTTGTGT | 83860 |
rs117841471 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7960877 | CAGGCATAACTCTTC[C/T]GTGTAATAAAGAACA | 83860 |
rs117853696 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7968123 | ACAGAAGTAAGGCAC[C/T]AAAGGTTAAACTAAA | 83860 |
rs117871295 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TAF3 | GRCh38.p7 | 10:7840175 | TTTTTTTTTTCGAGA[C/T]GGAGTCTCACACTGT | 83860 |
rs117924661 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | TAF3 | GRCh38.p7 | 10:7888269 | TTCTTTACTCCTTAA[C/T]CTTCCTAAGCTTTCC | 83860 |
rs117960290 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7890759 | TTCTAATTCTTTTGG[C/T]TTATTTTTAAGATAC | 83860 |
rs118003092 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | TAF3 | GRCh38.p7 | 10:7847861 | CAACCTCCACCTACT[C/G]GGTTCAAGTGATTCT | 83860 |
rs118050227 | snp | A/C/G | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7942228 | CGATGCATAAATTGC[A/C/G]TTTTGTCGATTTCAG | 83860 |
rs118050580 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:7890406 | TTGTAGTCTACGTTC[C/T]ATCATAGTAGAGTAG | 83860 |
rs118104510 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7878600 | GTATTTAAATCAGCT[A/G]TATTGGAAGGGAGTC | 83860 |
rs118131337 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7948323 | TGAACTCCCAGCTTC[A/G]AGCAGTCCTCCTGCC | 83860 |
rs118148048 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7924314 | CATGAAAGAAAGCGG[C/T]GGTTCTCTGCTAGCA | 83860 |
rs118148876 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7836007 | GCTGCTTTTCTTCAG[C/T]GCCATCATACTCCCT | 83860 |
rs118181937 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7885531 | CACCGAATCCTTTCC[A/T]CTTGGCCCCATCCAC | 83860 |
rs118182217 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7993097 | CTTCAACAGTTTAAC[C/G]AGGATCCAAACCAGA | 83860 |
rs137875803 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7869988 | GACCCCAAGTTTTGC[A/G]TATTTAAATTTATTT | 83860 |
rs137890526 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | TAF3 | GRCh38.p7 | 10:7976437 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTGTGT | 83860 |
rs137909952 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7979776 | AGTAATAGAATTTTA[C/T]GTAAAATAAAACTTA | 83860 |
rs137935963 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | TAF3 | GRCh38.p7 | 10:7951611 | AAATCATGTCCACCT[A/C]TTGATGAGAACAGCT | 83860 |
rs137936362 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7938473 | TGAATAATACTTGTT[C/T]AGTGACTAGATATGG | 83860 |
rs137942549 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7942550 | TTCTGAAACAAAATC[C/T]GCTGGGTTTTCCTGG | 83860 |
rs137950426 | in-del | -/TTT | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817850 | CAGGCAGCTTACCTG[-/TTT]TTTTTAAAAAAAAAA | 83860 |
rs137973421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830009 | CCAAGTGAATTCGTT[A/G]TGAAATGGAAGTGTC | 83860 |
rs137978283 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:8009742 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 83860 |
rs137993542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7968357 | TTTTCAATCTCCACA[C/T]TTATTTTACCTGCTT | 83860 |
rs138020759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7876095 | TCTTGTCTGTATAAT[A/G]AAGGGAGACGCTTAA | 83860 |
rs138051295 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7955705 | TATTTATAGTAGCTT[A/G]GAATTAACCTCCCAA | 83860 |
rs138079543 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7834571 | GTGTGTGAATAGATA[C/G]ATAGGTGGATAGGGT | 83860 |
rs138084348 | in-del | -/GTTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838943 | GTTTGTTTTGTTTTG[-/GTTTT]TTTTTAAATCCAGCA | 83860 |
rs138119440 | in-del | -/ACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959150 | GTCTCACACACACAC[-/ACAC]ACACACACACAAAAA | 83860 |
rs138125818 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7843118 | GCTGCACAGGCCAGA[C/T]CTTGTGAATATGTTC | 83860 |
rs138167219 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7924670 | TCTATTCTTTTTTAT[G/T]TTTAAATATGTGTAG | 83860 |
rs138208699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919122 | ATCTGAAAAAAAATG[A/G]GAGATTGAGTGCGAC | 83860 |
rs138209751 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7867217 | TGAGCCGAGATCATG[C/T]CACTGCACTCCAGCC | 83860 |
rs138225770 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7991071 | TTTTCTCTTTTGTAA[C/T]GATCTTTCATGTGAA | 83860 |
rs138226550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997562 | TTGTGGTGGGGAAAC[A/G]GGTAAAGAAATCCTG | 83860 |
rs138321679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901608 | CTTTGAATTCAATGG[C/G]TTGTTATATTTTAGA | 83860 |
rs138323401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882633 | TAAGGAAGAATTCTC[C/T]AACAGTCAGTGTCTA | 83860 |
rs138328814 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859767 | TGAGAAGAGATATTT[C/T]TGTCAATTTTATTCA | 83860 |
rs138333669 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958996 | ACACACAAAATTAGC[C/T]GGGCGTGGTGACGGG | 83860 |
rs138389975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866257 | GGGATGGAGCAGTCA[A/G]TAAATAGGCAGGCTC | 83860 |
rs138418184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7986563 | GTCTTCTTAGCTCCA[A/G]AAGTTTCCCAAGCTG | 83860 |
rs138436490 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7866813 | TCAGGTTAAATAAAG[C/G]TTAGGTTGAAAACAA | 83860 |
rs138531631 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:8014555 | CATGTCATAGACTCT[A/C]AAAAATTACTTTAAA | 83860 |
rs138537403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005842 | TTATGTAAGGCAAAC[C/T]TCAGTACACATTGAG | 83860 |
rs138546162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7889323 | TAACAAAAGCAACAA[C/T]AACTAATATTCAGTA | 83860 |
rs138549918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937091 | CATTCACCAAATGAG[C/T]GACCTCTTCATTGTT | 83860 |
rs138577542 | snp | C/T | 0.192401 | 0.243274 | intron-variant | TAF3 | GRCh38.p7 | 10:8008295 | GTAGAGACGGTGTTT[C/T]ACCATGTTGGCCAGG | 83860 |
rs138586365 | snp | A/C/T | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7900004 | ACATGTTAGGCGGCG[A/C/T]CCACTCATATCCAAC | 83860 |
rs138588441 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7947655 | TGGGGAGAAGCTTGG[C/T]GAGTTTGAGAAGCAT | 83860 |
rs138605789 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7919734 | AATGCTGTAGTCTTT[A/G]TACTGTTTTTATTGC | 83860 |
rs138616376 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7833626 | TTCAGTTTTTCTTTT[C/T]AACATCCTGTTCTGT | 83860 |
rs138625993 | snp | A/G/T | 0.000364271 | 0.013491 | missense | TAF3 | GRCh38.p7 | 10:7824401 | GAACTAGAAGACTAT[A/G/T]TTCACAACATTGAGC | 83860 |
rs138633255 | in-del | -/AAAC | 0.499839 | 0.00898417 | intron-variant | TAF3 | GRCh38.p7 | 10:7846619 | TAGAGGCTAACAAAA[-/AAAC]AAGGAGAAAAATGAT | 83860 |
rs138647829 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | TAF3 | GRCh38.p7 | 10:7888219 | TTGTTTTACAACCAA[G/T]CCTCCTAAAACACTG | 83860 |
rs138736424 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7883297 | AGAACAAACTAGTTA[C/T]TTTGTTAAATGTCTC | 83860 |
rs138770659 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887249 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGCTGGTTA | 83860 |
rs138842014 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7991783 | ATTTTGGTGAAGACC[C/T]AGCAGCTTTTTTGAA | 83860 |
rs138865701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920127 | GCATGTTGGCATGTG[A/G]CTGTATTCCCAGCTA | 83860 |
rs138867373 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7842690 | AAAGCCATGTTTTAA[C/T]TTTCTCCCCAATAAG | 83860 |
rs138872405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7924311 | AACCATGAAAGAAAG[C/T]GGTGGTTCTCTGCTA | 83860 |
rs138927463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952447 | GCACTCAGAATGCTT[A/G]TGTGGTGTCAGCAGC | 83860 |
rs138929345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830411 | TTATCAGCCAAATGC[A/G]TATCCCTAGACACAT | 83860 |
rs138938368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7908327 | TCTTCCCATGCAGGA[A/G]TGCAAGCCCTATGTT | 83860 |
rs138941446 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7954990 | GTGAGATTTAGAGTG[C/T]ACTCCATAGGTGAAT | 83860 |
rs138959903 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:8002528 | GAAAGGCTTTTTGTT[C/T]CTTTGAGGAACTACT | 83860 |
rs138979167 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818554 | TCAGGCTGGCGCGCT[C/T]CGTGCTGCTGGGGCT | 83860 |
rs138990521 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867658 | GGATGGCTACTGGCA[-/G]GTTTTTGATAAGGAG | 83860 |
rs138998835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853663 | AGCAAACTGCCTGGC[C/T]TGCAGCCTGATTCTG | 83860 |
rs139003877 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:8004295 | TCAAGCGATCCACCC[A/G]CCTCGGCCTCCCAAA | 83860 |
rs139083568 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885119 | GGCTACAGAGTGTCT[-/G]GTTTGGGTTGATGAA | 83860 |
rs139099335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896611 | TTGCAGTAAGTGGGA[A/C]AGAGGTCTTTCATAA | 83860 |
rs139121106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855854 | AGGGAGGTAAGAGGC[A/G]GGAGGATAGCTTGAG | 83860 |
rs139152455 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | TAF3 | GRCh38.p7 | 10:7838607 | GGCTGGTCTCAAACT[C/T]CTGACCTCAGGTGAT | 83860 |
rs139175073 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7943919 | AAAATCATTACCCCT[A/G]GTAAACCAAGATGAG | 83860 |
rs139192748 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7860889 | GCTGCAACCTCTGCC[A/T]CCTGGGTTCAAGCAA | 83860 |
rs139193533 | snp | G/T | 0.00716266 | 0.059414 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015581 | TGTTTAATTCTGGCT[G/T]TCTCTGAAATCCACT | 83860 |
rs139211814 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7932163 | CTGTTTTAAAAAGTA[A/G]AAGGAGGTGAACATG | 83860 |
rs139218204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8006056 | CAAACAAGGCCGGGC[A/G]CCGTGGCTTACGCCT | 83860 |
rs139232371 | in-del | -/TTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838363 | AGCCAGTTTTGTTTT[-/TTG]TTTTTGTTGTTGTTG | 83860 |
rs139273873 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | TAF3 | GRCh38.p7 | 10:7953869 | AGTGGATTAGTCCTA[C/G]TTAACACAGAGCTCT | 83860 |
rs139280027 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7910972 | TAGAGCTCTGGACCC[A/G]CTTAACCTTAGCTTC | 83860 |
rs139289457 | in-del | -/AC | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7969938 | CAAAACTAGGAAGAG[-/AC]AGCAGCATTCTAAAG | 83860 |
rs139295331 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7967037 | ACCTTGTTTTCTCCT[C/T]CTAACACACCTGTGA | 83860 |
rs139296768 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:8011915 | GTGCATGGTGTCTCA[C/T]GCCTATAATCCCAGC | 83860 |
rs139339275 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7895947 | CCGAAGCTGACCATG[C/G]GGGGGTGGAAATTCC | 83860 |
rs139354987 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7849436 | CATCCTGTAGATCTT[G/T]CACTTCTGGGACGAT | 83860 |
rs139355026 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899465 | CAGTTTACTTACACA[G/T]TTGCATTTCTCTTTG | 83860 |
rs139363345 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971082 | GTTCACCCAAGGCCA[C/G]CTCCCAGCCTTTCTG | 83860 |
rs139368212 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7969241 | TTGGGAGGCTAAGGC[A/G]GGAGGATAGCACCAC | 83860 |
rs139376350 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7879137 | ATGTTTAATATGGCC[A/G]TGTTTAGAGGTTTTT | 83860 |
rs139380366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957232 | ACCCACTGTCCTTCA[A/G]AGCTTCCCCAACAGC | 83860 |
rs139408206 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7836209 | ATCTGTATGCTGATG[C/T]CTCCCCAAACTGTCC | 83860 |
rs139438543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7972946 | AATAGCTCCATGTAA[A/G]CCATCAATATTACCA | 83860 |
rs139487000 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7992893 | CTTTTTATTCCCAAC[A/G]CATTTCCAAACAAAT | 83860 |
rs139501250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961088 | AGCTGCACTGGAGGC[C/T]GAGACTAGGTAGAAG | 83860 |
rs139510283 | in-del | -/TG | 0.358515 | 0.225221 | intron-variant | TAF3 | GRCh38.p7 | 10:7990037 | CCAGTTAAAATTAAC[-/TG]TATCTATTTTTAAGA | 83860 |
rs139515393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963686 | CTGGGGGAGGGATAG[C/T]GTTAGGAGAAATACC | 83860 |
rs139545926 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871901 | TCTAATATTTGTTCA[A/T]CACTTAAAATAAACA | 83860 |
rs139579664 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7925605 | GGTCAGGAGCTCGAG[A/G]CCAGCCTGGCCAACA | 83860 |
rs139611135 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TAF3 | GRCh38.p7 | 10:7877146 | TCTGTTACTTCCTTT[C/T]GGTAAACACAAATTT | 83860 |
rs139618451 | snp | A/G | 0.039522 | 0.134904 | intron-variant | TAF3 | GRCh38.p7 | 10:7976881 | TATAGGGAAGACATC[A/G]TCGCAGTTTTTTCTA | 83860 |
rs139637316 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TAF3 | GRCh38.p7 | 10:7977593 | TTCTGCATAGTCTTT[A/G]AGGTCCCACTTATCT | 83860 |
rs139695610 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861527 | ATGTCATGACTGAGA[C/T]GTGAAATCAGCCATT | 83860 |
rs139695614 | in-del | -/TG | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7968446 | AGGTAGAAGGAGCTT[-/TG]TGGGCTTTGGAATCC | 83860 |
rs139695736 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7910270 | TTAAGTATGAAGTGT[C/G]TAATAAAGATGTATA | 83860 |
rs139729137 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7949596 | CATAGAAGGAACACA[A/G]TAAGAATTTAATAGT | 83860 |
rs139759999 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7864262 | TACCCCAACCTGTGG[C/T]AACTACTGATCATTT | 83860 |
rs139767367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7921561 | TACATAGCTCCTAGT[A/T]AGACAAGGTATTATT | 83860 |
rs139768421 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869047 | AGAGTGTAAAACAAT[A/T]CATCGTAGAACAATT | 83860 |
rs139770510 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7867921 | TATTATATGTACTAT[A/G]TACTGTATTCTTACA | 83860 |
rs139778643 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7878285 | GTAGACTGGGTAAAT[-/AG]ATTGTGAAATATTAT | 83860 |
rs139782779 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7827136 | GCGAGTGTGCACACA[C/T]AGAAGGCCTGAAGGG | 83860 |
rs139798240 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | TAF3 | GRCh38.p7 | 10:8009987 | TACGATCTCGGCTCA[C/G]TGCAGCCCCTGCCTC | 83860 |
rs139803422 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923582 | TATTTGCTGTATAGC[-/A]AAAAAAACAAAACAA | 83860 |
rs139829754 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7897010 | CTTTCAGAGGCTGCC[G/T]ACATTCTTGACCACA | 83860 |
rs139858240 | snp | C/G/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7820540 | CACTCTGTCGCCGAG[C/G/T]GTGGAGTGCAGTGGT | 83860 |
rs139875395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978287 | AGAAAATTTGCTTTG[C/T]ATTCTCAGTGGTTCA | 83860 |
rs139948318 | snp | G/T | 0.101658 | 0.201233 | intron-variant | TAF3 | GRCh38.p7 | 10:7935510 | AATGGCGTGAACCCG[G/T]GAGGCGGAGCTTGCA | 83860 |
rs139948788 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7833551 | TTCTGTAGGGTTTTC[-/T]TTTTTCCTTTTTTGG | 83860 |
rs139963574 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8006991 | AGAAAGAGACAAGCT[A/G]GGACAGTCCACAGGC | 83860 |
rs139967300 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7982759 | GAGAGTTTTTCAAGG[C/T]AGTAAATTTAAAAAT | 83860 |
rs139996631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7864551 | TCCTCCTATCTAAGC[A/G]TAATAATGTGTCCTT | 83860 |
rs140002461 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7944748 | AGAATTAGACAAAAG[C/T]GATTATGGGAACTAG | 83860 |
rs140038202 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7835392 | CAGTGCTCCCTCTTC[C/T]ATCGTTTTTGCGGAA | 83860 |
rs140071584 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7838539 | GGTGTGCACCACCAC[A/G]CCTGGCTAATTTTTG | 83860 |
rs140099579 | in-del | -/ACAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846618 | CTAGAGGCTAACAAA[-/ACAA]AAAGGAGAAAAATGA | 83860 |
rs140120206 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7930646 | GTACCTGAGTACAGT[C/T]ATCAATATTTTTAAG | 83860 |
rs140141831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7990653 | ATTTTAGATTGTCTG[A/G]CATTTGGCTGTTCTG | 83860 |
rs140152215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869881 | CTATTTGTACTTTTT[C/G]CATTATAAATTGCTC | 83860 |
rs140159169 | in-del | -/CTGT | 0.00993419 | 0.0697739 | intron-variant | TAF3 | GRCh38.p7 | 10:8008857 | GCTAGAAATTTCTAA[-/CTGT]CTGGCCATTGAGGGG | 83860 |
rs140159711 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7951440 | CTGGGCCACACACTT[C/G]ATCACCCCGCAGGCT | 83860 |
rs140183971 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7884992 | AGTTTAATTTTTGTT[C/T]AGTTTTTTTTTTTTA | 83860 |
rs140192506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7911459 | GAGAAGCAGACCCAA[A/G]GGAAATAAAGTAATG | 83860 |
rs140192615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956670 | TAGCTGTGGTGATGA[A/G]TTTGTGCTGAGTCAT | 83860 |
rs140218010 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7829825 | GGAGTTATGCGTCCC[A/G]CTTTGAAGGTGGAAT | 83860 |
rs140271884 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7935924 | GGGAGATGGGAAGCT[C/T]GGGGAAGCCCTGCGT | 83860 |
rs140329040 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7888263 | TTTTGCTTCTTTACT[C/G]CTTAACCTTCCTAAG | 83860 |
rs140333033 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7961652 | TTATCTCAACAACAC[A/T]CTTTCTCTCATGCAC | 83860 |
rs140343762 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7995887 | AACGATTGACTTGAA[C/G]AATCAACATAAAACC | 83860 |
rs140347886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7923399 | TATGAAAATGGACTC[A/G]TGTCCTTTGGGGTGG | 83860 |
rs140360860 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7893688 | TCCCTTTGCTTCTAG[C/T]GTAGGCCTGGCCTAT | 83860 |
rs140367084 | snp | A/G | 4.99904e-05 | 0.00499927 | missense | TAF3 | GRCh38.p7 | 10:7965414 | AAGATAAGAGAGAGA[A/G]AGAAAAAGTGAAAGA | 83860 |
rs140369390 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7847498 | CGTACAGGCTGGAGC[A/G]CAGTGGTGCAGTCAT | 83860 |
rs140387892 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:8003416 | ACATATCATTATGTT[A/G]TGTAATGAATTATGT | 83860 |
rs140419135 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | TAF3 | GRCh38.p7 | 10:7852415 | CTCTCATTCTTTCTC[A/G]TTCTCTGTCTCTTTC | 83860 |
rs140420306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886113 | GTTTTTTGTAGAGAT[A/G]TGGGGGGGTCTCACT | 83860 |
rs140423926 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:8005605 | CAGACTTGCCTAATG[C/T]GTAAATGCCCTTGGG | 83860 |
rs140425693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7961011 | TAAGATGAGGAACCA[C/T]AAGCTCAGATTTGCG | 83860 |
rs140456354 | in-del | -/TATT | 0.0130973 | 0.0798567 | intron-variant | TAF3 | GRCh38.p7 | 10:7996028 | CTTCCAACTTCTGAA[-/TATT]TATTTACATACCTAA | 83860 |
rs140509166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898710 | GAAAGAAAGAGGTAG[A/T]CTCTCTTTAAGCTCT | 83860 |
rs140531981 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7867705 | TTGAATAGGAAGCAA[A/G]ATTAATGTCTTTGTT | 83860 |
rs140533885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821897 | AGTATTCCAGCTTAG[A/C]GAATCACATAAACTA | 83860 |
rs140543994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949257 | TCCACTGTAACGAAA[C/T]GCTGCCTTAATAATA | 83860 |
rs140584258 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7946458 | GCCAGGCACCATGGC[C/T]CATGCCTGTAATCCC | 83860 |
rs140626802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7901191 | TTAAGTTTAACTAAC[A/G]TAAAACTATAATGCA | 83860 |
rs140644736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979384 | AAAAAAAAGGCATTG[A/G]TAGTTATATTCAACT | 83860 |
rs140647092 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7938112 | AACAAAATAAAACTT[-/A]AGAGTCCTATGATTT | 83860 |
rs140651899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908365 | TTTTCCATTTTAACA[A/T]TAAAAATTGGAAAGT | 83860 |
rs140664244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984430 | TCTTACATAGATGCC[G/T]CATTAGAAGACTCAG | 83860 |
rs140686578 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7912037 | TAATGATTATTCATG[A/T]TTTACTTATTGCTTT | 83860 |
rs140692959 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7865978 | TGGTGCACCATGTTC[A/G]GCACCTTGACTTTCG | 83860 |
rs140720304 | in-del | -/ACCC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960890 | CCGTGTAATAAAGAA[-/ACCC]CAGCCGTTTCTACTG | 83860 |
rs140741027 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7846120 | CCCGCCACCACGCCT[A/G]GCTAATTTTTTGTGT | 83860 |
rs140744102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926751 | ATCTGAATTTGAGCC[C/T]ATTATATCTAAAATG | 83860 |
rs140756103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912665 | TTTGGGAATTTGTAG[A/G]TTTACTATTTAGAGA | 83860 |
rs140764580 | snp | A/G | 0.00716266 | 0.059414 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016739 | ACTGAAATCAGAATG[A/G]AGGTGCCTATATATA | 83860 |
rs140766556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7985260 | CTTACATCCCCCACG[A/G]CTTGTCGTCCAGGCT | 83860 |
rs140788810 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7866382 | GGGGCCTGTGATGGT[C/G]GCTGACCACGGAATT | 83860 |
rs140830422 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7958746 | GCTTCATAACTTCCA[C/T]GCGCGTTACTTATTC | 83860 |
rs140849591 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7853322 | ACCTCCCAACTCCAC[A/G]TGTGGGGGCATTACA | 83860 |
rs140863736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919416 | TGTTACTTAGGGTCA[C/T]TGTACACGTGAGCAA | 83860 |
rs140922817 | in-del | -/T/TT/TTT | 0.385741 | 0.209939 | intron-variant | TAF3 | GRCh38.p7 | 10:7857910 | TTTTTTTTTTTTTTT[-/T/TT/TTT]CTGCTAACCTTAGGG | 83860 |
rs140929212 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7966892 | AATGGGAATTCTGAT[A/G]TCAATAACTGAACAT | 83860 |
rs140952204 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7839171 | CCCAAAAATAACTAT[C/G]TACCTGGGTCAGCTC | 83860 |
rs140958606 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7963365 | AGGAAACAACAGAAG[A/G]CCAACTGGAAATACC | 83860 |
rs140982712 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TAF3 | GRCh38.p7 | 10:7973984 | AATACAAAAAGTAGC[C/T]GGGCATGGTGGCATG | 83860 |
rs140988255 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7929025 | GTTGCAAAGCAAAAT[A/T]AGCAGAAACTTGAAT | 83860 |
rs141014025 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7845355 | TGCTTTAGCATAGCT[G/T]AAGTGTAGTGTTGAA | 83860 |
rs141022276 | in-del | -/A | 0.291493 | 0.246533 | intron-variant | TAF3 | GRCh38.p7 | 10:7847985 | ATGGTGTCCAGGCTG[-/A]ATCGCAAACTCCTGA | 83860 |
rs141061037 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8004540 | TTTTTGTTTCATCTT[C/T]ATTCCTTAAAGATGT | 83860 |
rs141067350 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7888146 | TCTCTCCCATATGAA[A/C]CGTTTAAAGTTTTTC | 83860 |
rs141108227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7863124 | GAAACTGTGGTGGAC[C/T]AACTTCTTGGAAGTA | 83860 |
rs141139231 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7864174 | TAATGACAAATACCT[A/G]CCATTATAACATCAT | 83860 |
rs141145302 | snp | A/G/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7943283 | GCTCCTACGCATCAC[A/G/T]TTCTGCTTGCTCCTT | 83860 |
rs141172726 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7918384 | ATGCAGTGCCACATG[C/T]AGACTTAGAGTAAGG | 83860 |
rs141172898 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7820636 | AGTAGCTGGGACTAC[A/C]GGGATACGCCACCAT | 83860 |
rs141184021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922956 | TTCTACACTTAAACC[A/G]CTTAATAACATTAGT | 83860 |
rs141227944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840816 | ACTGCTTACAGCCAC[A/C]TAGAACTTTGCTATT | 83860 |
rs141277288 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7960137 | ATTGGGATTTATGAA[-/C]CTCTGTGGAGTAGGA | 83860 |
rs141306985 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7875916 | ACGACTAATTTTACC[A/G]ACAGAAAATAATTGA | 83860 |
rs141336740 | in-del | -/A | 0.319376 | 0.240181 | intron-variant | TAF3 | GRCh38.p7 | 10:7966022 | GCAGCTTAAAAAAAA[-/A]CAAATCTGGGTTCTT | 83860 |
rs141340637 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7947595 | ACGAGAGAAGCAGCC[A/G]TGAGCCGACCTGGAG | 83860 |
rs141354280 | in-del | -/T | 0.0368353 | 0.130617 | intron-variant | TAF3 | GRCh38.p7 | 10:7904779 | ATTTGAAACTTGGGG[-/T]TTTTTTCCAGATTCT | 83860 |
rs141373321 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7981378 | CTTTATCAGCAAGCA[C/T]CAGAGAAGGGGTGAC | 83860 |
rs141373740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7951137 | TTTCTCTTAAGAGCA[A/G]TGGTTCAGTATTTGT | 83860 |
rs141384371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907588 | TATGAGGGTAATACA[A/G]TAGCCAGAAGTTTGG | 83860 |
rs141405513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955427 | TTTAAATACGTTTAA[C/T]TTTTGATGAAATATA | 83860 |
rs141417289 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TAF3 | GRCh38.p7 | 10:7961911 | CTGGAGTGCAGTGGC[A/G]CAATCATGGCTCATT | 83860 |
rs141425092 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7827980 | AAACACATGACAGCG[A/C]ATATTAGTTCTCGTC | 83860 |
rs141435193 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7992290 | AGACAACACTCTCTG[G/T]GTTTACATTTTGAAA | 83860 |
rs141439100 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7889030 | CTACACGTGGGATAT[C/T]GGAGCTGCTTTTTAT | 83860 |
rs141446240 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7842862 | GCAGGCCCACATTTA[C/T]AGTCTGTTCCTGAAA | 83860 |
rs141447291 | in-del | -/T | 0.299411 | 0.245069 | intron-variant | TAF3 | GRCh38.p7 | 10:7824301 | AATAATTTGATTTGC[-/T]TTTTCACTTTGTTTC | 83860 |
rs141510188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974451 | CTTAGTGTCAATCAG[C/T]GCTAATCCAGACCAA | 83860 |
rs141534875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900083 | AAGATATCCATCCTG[C/T]GTAATGGTGTAAAGC | 83860 |
rs141549017 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:7896043 | GGAATAGGAGAATTC[A/G]GAGAAGGAAAAGGAG | 83860 |
rs141573057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7972285 | ATGGAAACAAAAATC[C/T]GGGAAGAAATTTTAA | 83860 |
rs141594445 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7936574 | TGAACAGAAAGTACT[A/G]AGGGTTCCCATTCAC | 83860 |
rs141597555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7855369 | AGGCCTGTGATAACA[C/T]ACCAGACCAGAAGGC | 83860 |
rs141598778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862064 | AGCTTTCTGCTACAC[A/G]TGCAGTTAAGTTTGA | 83860 |
rs141606729 | snp | A/C/G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7940612 | GAAGGGAATTATTAT[A/C/G/T]TGAGACAGTTCTTGT | 83860 |
rs141621769 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TAF3 | GRCh38.p7 | 10:7904176 | CAGTCTCGCATAGTG[A/G]GGTTGGGACACGCTC | 83860 |
rs141662620 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817149 | TTTGTGAAATCCAAG[A/G]CGCAAGAGAGTTTCA | 83860 |
rs141694679 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8014389 | GACAAAGCCGTGGCT[C/G/T]GGAAGACTTCTATTC | 83860 |
rs141719582 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7838503 | TCTCCTGCCTTAGCC[C/T]TCCAAGTAGCTGAAA | 83860 |
rs141772836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949050 | CTGACAGCCGCTCTC[A/G]GGTCAACAGTGTCAG | 83860 |
rs141789851 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7842232 | AGGCTGAAGTGCTGT[A/G]GCACGATCGTAGTTC | 83860 |
rs141862085 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7848942 | TAGTTTAACTGTTTC[C/T]CAGTAGGGTGTTTTT | 83860 |
rs141877491 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7915040 | CCGCCTCCTGGGTTC[A/G]CGCCATTCTTCTGCC | 83860 |
rs141925782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7995356 | ACTCCAAAGTGGAAG[C/T]TGTATAACAAAATAC | 83860 |
rs141947958 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7960098 | CCTGCCTAAGCCAAA[C/T]CTTTATCATTCTGTT | 83860 |
rs141950566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960374 | GGGGTCAGCAAACGT[C/T]TTTTTGTAAAGAGCT | 83860 |
rs141955872 | in-del | -/AAAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846620 | AGAGGCTAACAAAAA[-/AAAC]AGGAGAAAAATGATC | 83860 |
rs141960665 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7920232 | GCACTCCGGCCTGCG[C/T]GACAAAATTTATTTC | 83860 |
rs141970364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854679 | CGGGGGGAGGGGAGC[A/T]TCACTAGGAAATCAG | 83860 |
rs141973049 | in-del | -/GGT | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7999099 | AGCAGATGGAAGGAA[-/GGT]GGTAGGCAGGGAGGA | 83860 |
rs141973530 | in-del | -/TGAATCTTTCCAGGTGTTCACTTTTTTTTTTAAACCTAGAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901012 | TGGTGTGCTTGTGGT[lengthTooLong]GATCATCCAAAAATT | 83860 |
rs141999736 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7875164 | TTTATATGGTAGTAA[A/G]TAATCACCATTGCTG | 83860 |
rs142013441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832803 | GATCTGCCCACCTCA[C/G]CCTCCCAAAGTGCTG | 83860 |
rs142027780 | in-del | -/GTGC/TGCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828901 | AGCTGGGTGTGGTGG[-/GTGC/TGCT]TGCCTGTAGTCCCAG | 83860 |
rs142067096 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7931738 | TCAATCAGGCAACAA[A/G]TATTAATACTGAGTG | 83860 |
rs142079307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7836674 | AACATGAGAATTAGC[A/G]TTGACCTCTTCTCTC | 83860 |
rs142081686 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842344 | TTTTAATTTTTTGTA[A/G]AGATGAGGTTTCAGT | 83860 |
rs142083812 | in-del | -/ATAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935286 | TTTCTAAATAAATAA[-/ATAA]ATAAATAAATAGAAG | 83860 |
rs142114284 | in-del | -/A | 0.0513262 | 0.151752 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016102 | TTTATTTTTAATGTT[-/A]AAAAAACATCAAATT | 83860 |
rs142117945 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | TAF3 | GRCh38.p7 | 10:7860202 | GCTGAAGCCTGGGAG[A/G]CAGAGGTTGCAGTGA | 83860 |
rs142119658 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7990295 | CACAATTGTGAGTGG[C/T]AAATGGCCATGTTCT | 83860 |
rs142157034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7867902 | GATTAACACGTATTT[C/T]GTATATTATATGTAC | 83860 |
rs142169528 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7856991 | AATTCCATGTAGCCA[A/G]CTGATTCTCAGAGAA | 83860 |
rs142267405 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7864941 | TTATAGTTTTAGGTT[G/T]TGGGTGGCTGGGGTG | 83860 |
rs142271962 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7945901 | CTGCTAGTAAAATCT[A/G]TGAATAGAGAAACCT | 83860 |
rs142306012 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878706 | ATGTATGTATGTATG[A/T]ATGTATGTATGTATG | 83860 |
rs142307269 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TAF3 | GRCh38.p7 | 10:7976501 | CTCACTGTAAGCTCC[A/G]CCTCCCGGGTTCACA | 83860 |
rs142331838 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TAF3 | GRCh38.p7 | 10:7941395 | TAGATACAGGTCAGC[A/G]GGGTGGGGATTATTT | 83860 |
rs142358103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938967 | AAAGCCGTAAGGATA[A/G]TAGAGCAAGGGAAGA | 83860 |
rs142363092 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818148 | CTGAGGCAACACCAG[A/C]GCAGGTCTGCGTTTG | 83860 |
rs142386559 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7900970 | GCTTCTTGAAGTAGC[A/G]GTGTATGTAGATATT | 83860 |
rs142398088 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980232 | ATCATCTTTTGAAAT[G/T]AGGAAAAACGAAAAA | 83860 |
rs142417406 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | TAF3 | GRCh38.p7 | 10:7863553 | AGGCGGAGGTTGCAG[C/T]GAGCTGAGATCGCCC | 83860 |
rs142425388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942551 | TCTGAAACAAAATCC[G/T]CTGGGTTTTCCTGGA | 83860 |
rs142442208 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7878203 | AGCTTGTACAATTTT[A/G]GGAGCCTTTTTAAAG | 83860 |
rs142444458 | in-del | -/ACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939578 | AAATAGAAGAAAACT[-/ACACAC]ACACACACACACACA | 83860 |
rs142451882 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7858193 | TTGGCCTGGCTGTTA[A/G]GAATCACTGTCTTTT | 83860 |
rs142464726 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7984112 | TACAAATTCAGCAGT[C/T]CCAAACCCATAGATC | 83860 |
rs142481793 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820157 | GTGTCCTTTGCCCGT[C/G]GCCCACCAATAGTAT | 83860 |
rs142490255 | in-del | -/T | 0.168785 | 0.236441 | intron-variant | TAF3 | GRCh38.p7 | 10:7977525 | ATTTGACGTAAAGGA[-/T]TTTTTTTTTCTTGTT | 83860 |
rs142509484 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:8006605 | AGATGATCACCCTTG[C/G]AGGAAACAAATAGAG | 83860 |
rs142540070 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7876675 | CTTACTTGAAAATAC[A/G]GCTATATTGTCCTAA | 83860 |
rs142566252 | in-del | -/AAAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865503 | AACAAACAAACAAAC[-/AAAG]AAACAAACAGAAAGT | 83860 |
rs142604439 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7937204 | GGTAAATGCCAGGGA[A/G]TGTGATTGCTGGATC | 83860 |
rs142606377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7830775 | AGGCGTGAGCCACCC[C/T]GCCCAACCATGTCAT | 83860 |
rs142614117 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008403 | CTTGCCCAGCCTGAA[C/T]GGTCAATCTTTAAAA | 83860 |
rs142614521 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7939853 | GAGGTCCTATAGCCA[A/C]CTAAAAGGAGTCCTA | 83860 |
rs142614701 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8011480 | GATGTCTCTCTGTGT[C/T]GCCCAGGCTGGTCTC | 83860 |
rs142687268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913362 | GCAGCCCAAGTCACA[A/C]AGCAGCCACTCCAGC | 83860 |
rs142717347 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997657 | GTGATCAAATCCTCC[A/G]AAAGCTGTAATGCTG | 83860 |
rs142737773 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936512 | TCTTTTTTTTTTTTT[-/C]CTTAATAGACTTTAT | 83860 |
rs142772229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7956522 | AAATAATTTTACAGT[C/T]AAATGTTGACCTGGA | 83860 |
rs142800792 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7949283 | TAATAAAGCACAGCC[A/G]GAAATAAAGAGTGGG | 83860 |
rs142806406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8001644 | GATACTAGAAATTGT[A/G]TCCTACCCCAAGACT | 83860 |
rs142807870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7952715 | TGCATCATATTCACT[C/T]TACTATTAATTTCTT | 83860 |
rs142813928 | in-del | -/T | 0.0693013 | 0.172766 | intron-variant | TAF3 | GRCh38.p7 | 10:7912828 | GCGAGGCACTGGTGC[-/T]TTTTTTTCCTTTCTG | 83860 |
rs142814323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877880 | ACCGTGTGTGTTATT[C/T]TGAGAAGGGACTAGT | 83860 |
rs142825672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835119 | GCCTTTAGAACACAG[A/G]TGTCCAATCTTTTGG | 83860 |
rs142827931 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7882856 | AATTCCTAAGTATTC[C/T]TTACGTAGATTCCCC | 83860 |
rs142831856 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959776 | TTTGCCAGTTCTAAT[C/T]TGATAGAATTGCACA | 83860 |
rs142847119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7830443 | AATTTAATGTTCTTC[A/G]CACATGCACACCTTT | 83860 |
rs142859282 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7909400 | TTGGCCTCCACCACC[A/G]TCTGCCCCTCAGAAC | 83860 |
rs142918990 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7834099 | TTACATGTTTTGGGC[A/G]TGAGCCCCTTGTCAG | 83860 |
rs142955695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839077 | TGTGTGATCGGACTC[C/G]TGCCCACTTGACATG | 83860 |
rs142961751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7921681 | TTGAAAATGATTACT[A/G]CAGAGAATATTTCAG | 83860 |
rs142982628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7933876 | GGATTCAAAGATGCA[C/T]GTTTTCCCCCCGATT | 83860 |
rs142993307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7823854 | TGACCAGGTTGGTCT[C/T]GAACCCTTGACCTTG | 83860 |
rs143003127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7909231 | ACTGGATCAGAGCCT[C/T]TGGGGCCCAGGCTCT | 83860 |
rs143020665 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7980278 | AATTATACCTTCTAG[C/T]TGGAAGATCTTTAAG | 83860 |
rs143095288 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7917977 | CTTTCAGTGTTTAGA[C/T]ATGACAAAGAGCAAA | 83860 |
rs143142704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961373 | ATGCATCATCTCACG[C/T]GTTCTCCATCTGTGC | 83860 |
rs143153186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7897153 | GAAGAGATCAGGCCC[A/G]CTTGGCAAGTCTCGC | 83860 |
rs143163822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968654 | AAGATAGATGCTGTA[A/G]TTATTATCACTTTAA | 83860 |
rs143169334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7851600 | GCTTCACCCGTATCT[A/G]CTCATGGCCAGTCTT | 83860 |
rs143171499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841436 | TTAAAATTATAATTT[A/G]GGATTCTTAAAGGAA | 83860 |
rs143202804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7923249 | AGTGTTTAAAAAAAT[A/G]TTTTTTAAAAAATAG | 83860 |
rs143204386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963379 | GGCCAACTGGAAATA[A/C]CGAGCAATTTCCAGA | 83860 |
rs143219616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967151 | ACAGCTAGCAAGAGC[C/T]AGGTCAGTTACACTG | 83860 |
rs143237663 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822558 | TTCCACCACAGCCCT[C/T]GCCTCTACTGCAGCT | 83860 |
rs143247722 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7933290 | ACATGAATTAAATTC[C/T]AGATCAGAGGCACAT | 83860 |
rs143275629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7849672 | TGGGGGGGTTCATGC[A/G]AACTTTTTTTTTTTT | 83860 |
rs143284199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7930217 | AACAAACAAAAAGAT[A/G]CAGCCTAAGAGAAAT | 83860 |
rs143337482 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7869447 | TGTGAAGGTCTTTCC[A/C]TGTCTGTTAACTTAT | 83860 |
rs143340117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853734 | GGGTGACTGCTTTGG[C/T]ACTACAATGGCGGAG | 83860 |
rs143349650 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7859893 | CATAATGATTATTAC[G/T]CATCCTTGGTTCATG | 83860 |
rs143354381 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7937454 | GGAACATCTTTTCAT[C/G]TTTTCCTGTGCCTAT | 83860 |
rs143391251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7935595 | TCTCAAATAAATAAA[C/T]AAATAAAGCAAGCAA | 83860 |
rs143396388 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7870032 | GTGAGCATCTTTAAA[A/C]AAATTAGATAATTAG | 83860 |
rs143407870 | in-del | -/TCTCTGGGTTAGGCGCTGTTTAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947358 | CAGCTGTGAGGGCCT[-/TCTCTGGGTTAGGCGCTGTTTAG]TCTCTGGGTTAGGCG | 83860 |
rs143409198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8007197 | TACCATGGAATACAA[C/T]ATAGTAATTAGAATA | 83860 |
rs143441875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837679 | AATTAGCCAAGAGTG[A/G]TGATGTAAGCCTGAG | 83860 |
rs143458713 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7830243 | ATCTGAAGGAAATTT[A/G]AACCCTTTCTCCCAG | 83860 |
rs143510330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893272 | TTCCTGAAAGAAAGC[C/T]TTGTTATTTAATAAT | 83860 |
rs143578710 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | TAF3 | GRCh38.p7 | 10:7915383 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 83860 |
rs143581062 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | TAF3 | GRCh38.p7 | 10:7982007 | AGTTACAAAAATAAT[C/G]ATTTAAAATATTTTT | 83860 |
rs143590481 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:8000413 | TGAGCCACTGCACCC[A/G]GCCTTTTTCTTTTTT | 83860 |
rs143604682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986077 | GCATGAGCCCCCATG[C/G]CCAGCCTTTCATTCT | 83860 |
rs143619519 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7880607 | TTGTTTCCTTTAAGG[G/T]CCATTTCTTATAAAT | 83860 |
rs143628660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7914059 | CCTCTTTTAGATACC[A/G]ATTCAAAGAAACTGA | 83860 |
rs143650272 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:8008119 | TTTTTTTTTTTGAGA[C/T]GAAGTCTCACTCTGT | 83860 |
rs143663691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894496 | GTCAGTGACCTGATC[A/G]ATTCCTAGATGGTGA | 83860 |
rs143668898 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966747 | ATTACCAATAAATTC[A/G]GAGTATTTTTAACTT | 83860 |
rs143696343 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7867438 | TTTAAATTACAGCTC[A/G/T]CAAATATTTCCTGAT | 83860 |
rs143723634 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848402 | AAACTCCTTTTTCAT[C/T]TCCTTTCATGTACAG | 83860 |
rs143740301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7942125 | GTTCTGTAATGTTCT[A/G]TTAGTTATGTTCTTA | 83860 |
rs143755873 | snp | A/G | 3.31516e-05 | 0.0040712 | intron-variant | TAF3 | GRCh38.p7 | 10:8013861 | CCAGGGCGCCCTGCC[A/G]GCCACACTCATTAGG | 83860 |
rs143758509 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7832575 | TTTTGAGACAGTCTC[A/G]CACTGTCACCCAGGC | 83860 |
rs143770164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819478 | ATGTACTTTCACTTA[C/T]GTCTCGGTTACCAGT | 83860 |
rs143773542 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7899552 | AGAACATTGCTTTCT[A/G]TTTATATTCCATGTG | 83860 |
rs143814710 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | TAF3 | GRCh38.p7 | 10:7954401 | ATAGGCAAATGAGTG[A/G]ATTAGTTCTAGTTAA | 83860 |
rs143873087 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7831838 | TGGTATAAATTATCT[A/G]TCCAGGAAACCCTGG | 83860 |
rs143928482 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7911755 | GTAACAAATAAGCAG[G/T]GTTTACATCTTTCTT | 83860 |
rs143930292 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7956799 | ATTTCTTATTTGAAG[C/T]ATAGCATTCACATTT | 83860 |
rs143941283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8003055 | CTATTGCTAGATGTT[C/T]CTCTGGGCATTAGAA | 83860 |
rs143943770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968515 | TTCTTTAATCCTTAA[A/G]TATTTCATCTTTAGA | 83860 |
rs143979556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7855982 | TCTACTAGTATTCTA[A/G]GAGAGGACAAGAAAA | 83860 |
rs143980172 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7931395 | CTGAAATTCATTATG[A/T]CAGAGTCCCCTTACT | 83860 |
rs143981207 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7931286 | AGTCAGGTAACTTCT[A/G]TGTGTGCTACTGCTG | 83860 |
rs143984803 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7935103 | CCAACATGGTGAAAC[C/T]GCATTTCTATTAAAA | 83860 |
rs143993361 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7914121 | TTTTTTGAGGAAATT[G/T]GTATATAGACTGGGT | 83860 |
rs144013757 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016312 | TAGTGTATGAATTAG[C/T]CATATTTTAAAACAT | 83860 |
rs144033060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005943 | CCATGTAGTAGTAAC[A/C]TGTGTTAATTTATGC | 83860 |
rs144057494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889447 | GTCTGTTACAGATGA[A/G]GAAGCAGAGGCAGAA | 83860 |
rs144106287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969879 | CACCAACCTCCCATC[C/T]TCGCAGACCCTCTGC | 83860 |
rs144122032 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:7900558 | ACCAATGCTGGCATC[A/G]TTGAAAACTCCTGTG | 83860 |
rs144133020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852476 | CTGCGTTGTTTGTCC[G/T]GTAGAGTTTTTTATA | 83860 |
rs144160687 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7973152 | TATAGAGTTGTGAAG[A/G]TAGAGTTGAATAATG | 83860 |
rs144165628 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7932230 | TAAAATATTATAAGG[A/G]ATGACCTGTGCACTA | 83860 |
rs144194348 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7872107 | ATTTCCATAATTAAA[A/G]TTTGTTCTTCCTGGC | 83860 |
rs144196493 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:8000215 | GCTCACTCCTGGGTT[C/T]AAGCGATTCTCTAGC | 83860 |
rs144209853 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7880196 | GTGAGCTATGATCAC[C/T]CACTGCTCTCCAGCC | 83860 |
rs144220776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7957683 | AGAGTCCTTTTCTCC[C/T]GTTTCAGAACACTAA | 83860 |
rs144234593 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8003418 | ATATCATTATGTTGT[A/G]TAATGAATTATGTAA | 83860 |
rs144237805 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7831372 | TTTTTTTGAGATGGA[G/T]TCTCACTCCATCGCC | 83860 |
rs144279452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886475 | CAAAATATATAATAA[C/G]CAAAGAAAAGTTTGG | 83860 |
rs144286909 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7992036 | CAAATTCATTTTCAT[A/G]TGAAAGCATCTTTTA | 83860 |
rs144338291 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7961042 | TGTTCGGAAGATCAC[C/T]GTAAGACGACGTGAG | 83860 |
rs144391685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7822020 | TGTTCAACAGAGTGA[A/G]ATCAGGTTATGGAAG | 83860 |
rs144392927 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7984706 | TGTTATCAAGGTCCA[C/T]GATCACTAATTGAGT | 83860 |
rs144412555 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7904849 | TAACTGGCTGAGCTC[A/C]TGGAAGCTGGCTGTG | 83860 |
rs144413605 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7924725 | AAACGCTCATAATCT[C/T]ACCACCCCAACAGAA | 83860 |
rs144434122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7989406 | TGCTGAATGCTGGAA[A/G]CCATTGGGTTTACTT | 83860 |
rs144450238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7825213 | ACACAAGTACACGAT[A/G]TTTTTTCTTATAAGA | 83860 |
rs144459818 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7826792 | AATGCAATTCTTTGG[C/T]TACCATTTAAAAATA | 83860 |
rs144475180 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:8006067 | GGGCACCGTGGCTTA[C/T]GCCTGTAATCTCAGC | 83860 |
rs144484464 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7934885 | TGCGGCAGGCATGTT[C/T]TAGGTGCTGAAAATA | 83860 |
rs144516426 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7890632 | CTTGCTTTTCTTGCA[C/T]AAAACACATTCTAGC | 83860 |
rs144526187 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | TAF3 | GRCh38.p7 | 10:7993299 | TCCTCCCACCTCAGC[C/T]TCCCAAGTAGCTGCA | 83860 |
rs144541232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7950714 | AATTCAGTCGCATGC[A/G]TTGCCTGTTCCCAGC | 83860 |
rs144591772 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7939505 | GTAACTACCAGAAAT[A/G]AAAGGTATCCCACAT | 83860 |
rs144630354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901076 | TCCACTGCATTTGAT[C/T]ATAATTTATTTTTAA | 83860 |
rs144639336 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8014427 | AGAGGATGAATGAAC[A/G]GATGAGTCTCTGCAG | 83860 |
rs144648356 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7974355 | TGGGCAAGTTGATAC[A/G]TTAAGATTTCAGTGT | 83860 |
rs144652058 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7838616 | CAAACTCCTGACCTC[A/G]GGTGATCCACCCACC | 83860 |
rs144693973 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7906310 | CAAGATATCTGATAA[C/T]GCCCACATTTAAATA | 83860 |
rs144712858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947602 | AAGCAGCCGTGAGCC[A/G]ACCTGGAGGAACAGC | 83860 |
rs144732628 | in-del | -/ATGTATGTATGTATGT | 0.483126 | 0.0902898 | intron-variant | TAF3 | GRCh38.p7 | 10:7878691 | TAATTAATTCAACCA[-/ATGTATGTATGTATGT]ATGTATGTATGTATG | 83860 |
rs144737917 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7977879 | CCCACGTTTGCTGTT[G/T]ATTTGTCTTAATTTT | 83860 |
rs144775480 | snp | C/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881407 | CAAGTCAGCAGTATA[C/G/T]GAAAACTTCAAAATT | 83860 |
rs144775772 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7932762 | GGCTGACTACAGCCT[C/T]GACCTCTCAGGCTGA | 83860 |
rs144780952 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:8002970 | TCTTGCCTTAAAGTC[-/T]TTTTTTGTGTGGTAT | 83860 |
rs144788034 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7888187 | TCTTCCTCTAGGCCA[C/G]GATCTACACCCCTTC | 83860 |
rs144809483 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839179 | TAACTATGTACCTGG[A/G]TCAGCTCATGCTGGC | 83860 |
rs144820963 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:8002624 | GGTCAGTTTCTTTCA[C/T]TGTTCAGTATATTTT | 83860 |
rs144859987 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7884512 | CTGTCTCAGCCTCCC[A/G]AGTAGCTAGGATTAT | 83860 |
rs144865251 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7960177 | TTGAAATTTAGAAAT[A/G]TAATATTAATAAGTG | 83860 |
rs144872353 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7841369 | TCCCTGCTTTCCTAG[A/G]GCTTACAGTCTACTT | 83860 |
rs144873878 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7845385 | ATTTTATGTCCTCCG[G/T]TTTTCGTTTAATTAA | 83860 |
rs144922604 | in-del | -/GAAT | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7981745 | TAACAAAGGTGCTGA[-/GAAT]GAATGTGATGCTTTC | 83860 |
rs144990815 | in-del | -/T | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7981808 | TTCACAGAGTTTAAC[-/T]TAAGCCTTGTGGGGG | 83860 |
rs145041981 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7923022 | TTCTGGTCTGCCTAC[C/G]AAACAGTTAATTATC | 83860 |
rs145044878 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8004440 | AAAGGGGCCCTAGGA[C/T]GAAAAATTTGAGAAT | 83860 |
rs145082400 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7902231 | GAGTTCGAGATCAGC[C/T]TGACCAACATGGAGA | 83860 |
rs145083259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951168 | TAGTTCAGTGTTACC[A/G]TAACTACTGCAAATA | 83860 |
rs145099973 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7961297 | ATGCCATCATTATCG[C/T]GAATCGGTAGCATAA | 83860 |
rs145110594 | in-del | -/AATAAATAAATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859261 | GTGAGACTCCATCTC[-/AATAAATAAATA]AATAAATAAATAAAT | 83860 |
rs145110802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829439 | TTGTCACGTCTCCTT[A/G]GACTTTTCTTGGCTG | 83860 |
rs145117017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7907645 | TTAGATGGGTGATTC[A/G]TAGCAGAGCCTTTAA | 83860 |
rs145146347 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:8000074 | CCTTAAAAATTCCTA[A/G]CAACAGTTTAGACGT | 83860 |
rs145160445 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7925913 | TGCTGGGATTGTAAT[A/G]ATCTCTTAAGACTGG | 83860 |
rs145161328 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7911294 | AGTCAGTGAAATCTG[A/G]CCTAATCTGGGACAG | 83860 |
rs145173471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7983715 | GTAGTGGCGTGCACC[C/T]ATACTCCCAGCTACT | 83860 |
rs145221127 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7861920 | CCTTCTGAGACGCCA[A/G]TTAAACTTGTGTTAG | 83860 |
rs145234549 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7864858 | GTTTTGTACTCTTTG[C/T]GCCCTAAGAAATCTT | 83860 |
rs145237919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7864424 | GTGTCACATAGTTAA[C/T]TCTTTGTGGTAAGGG | 83860 |
rs145244596 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7970657 | GAGCACCTGTTTAAC[C/T]GCCATATTTTAAAGA | 83860 |
rs145251733 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7933226 | AGGAATGCAAACGCT[A/G]TGGCATTTTGCTTTT | 83860 |
rs145275293 | in-del | -/CA | 0.0490535 | 0.14873 | intron-variant | TAF3 | GRCh38.p7 | 10:7858830 | GTGTGTGTGTGTGCG[-/CA]CGCGCCTGCATGTCA | 83860 |
rs145293233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853589 | AGTTGCTCACATCAT[C/T]GACACGTGAAATTCT | 83860 |
rs145300604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7836277 | GTTGGCCATTTCCAC[A/G]TTTTCTTTTTTCTTT | 83860 |
rs145315535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7916922 | ATTGGGTTCGTACTC[A/G]ATTATTTTCTTCAGA | 83860 |
rs145326079 | snp | A/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817855 | AGCTTACCTGTTTTT[A/T]TTAAAAAAAAAAAAA | 83860 |
rs145354439 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TAF3 | GRCh38.p7 | 10:7979734 | TAAATTAAAATAGAG[C/T]GAGAAAGAAAGAGGA | 83860 |
rs145381694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975297 | TAGATGTGTAGAAGG[A/G]GAAAGAAGGTCATGG | 83860 |
rs145385059 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7908791 | TTGGATCTTCTGTGT[A/T]TGAAGTGGTTATGAA | 83860 |
rs145403264 | snp | A/G | 0.0108389 | 0.0728145 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965727 | AAAAGAGAAGGAGAA[A/G]CACAAGCATGAAAAA | 83860 |
rs145403361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924267 | TGTTTTATTTTGTGC[A/T]AACCCAATGAGAAAG | 83860 |
rs145447351 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7842270 | CCTCTGCCTCCCGGG[C/G]TCAAGCAGTCCTACC | 83860 |
rs145460708 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016402 | TGGAGTCGACCTCTT[C/T]GGAGCACAGGGTGTC | 83860 |
rs145470040 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928213 | CTGTTTTGTATATTC[C/T]ACTAAAATATAAGTT | 83860 |
rs145505055 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885250 | TTATATAAATTTTGA[-/AC]CACACACACACACAC | 83860 |
rs145534198 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7994300 | GATCTGGAATTAGCA[A/G]TTTCTCCAAGGAACA | 83860 |
rs145555105 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7885272 | CACACACACACACAC[A/C]CCCCCACACACACAC | 83860 |
rs145576525 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7861396 | CAAGCATGAGCCACC[A/G]CACCCAGCCAACAGG | 83860 |
rs145628224 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | TAF3 | GRCh38.p7 | 10:7927622 | TGCTCTATATTTTAA[C/G/T]GTCAGATAATGCCCA | 83860 |
rs145664339 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:8000219 | ACTCCTGGGTTCAAG[C/T]GATTCTCTAGCCTCA | 83860 |
rs145674045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7997545 | CTATTTATGTCACTG[A/G]TTTGTGGTGGGGAAA | 83860 |
rs145692152 | in-del | -/TTTGTC | 0.34989 | 0.229177 | intron-variant | TAF3 | GRCh38.p7 | 10:7825590 | TGGACTTGGACATTA[-/TTTGTC]TTTTTATGACTGGCT | 83860 |
rs145692622 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7950470 | TGGATTTAGAGAAAC[A/G]TCTTACCAGATACAG | 83860 |
rs145696913 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:8001210 | GGTAAAGAGCTTGCA[C/T]GTTTTTAAGTTTTCC | 83860 |
rs145722072 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7827462 | TACCAGCCTGGGCAA[C/T]GTCATGAGACCTCAT | 83860 |
rs145731643 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TAF3 | GRCh38.p7 | 10:7929543 | GCTGAGACTACAGGC[A/G]TGTGCCACCACACCC | 83860 |
rs145755850 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7936399 | GTTTAAAGCATTATA[C/T]GATTAAGGATCAAAT | 83860 |
rs145762902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894232 | CTTCTCCTACCCCTA[A/G]GCAATACAAATTCTC | 83860 |
rs145773834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832807 | TGCCCACCTCAGCCT[C/T]CCAAAGTGCTGGGAT | 83860 |
rs145794812 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7874119 | AAGCTGTGAGCTTGT[C/T]ATATAAAATATACCT | 83860 |
rs145810241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866158 | CCTCCAGTATGCATA[C/T]GTTCCTTTTATCATT | 83860 |
rs145824049 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | TAF3 | GRCh38.p7 | 10:7979275 | CATGAACCTGGGAGG[C/T]GGAGCTTTCTGTGAG | 83860 |
rs145874212 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7823206 | GGTATAATTCATTCA[A/G]TAGGTATTTATTGAG | 83860 |
rs145885560 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825842 | TCTTGCTTTCAGGTG[-/T]TTTTTTTTTGGGTCT | 83860 |
rs145929100 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7939107 | GGTCATCAGGAACTC[A/C]AGAAGGCAGGGATGT | 83860 |
rs145961980 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7896906 | GAAGGCCCTTTTCCA[A/G]CCTTCTTTATTGGTA | 83860 |
rs146049799 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7956668 | TCTAGCTGTGGTGAT[C/G]AATTTGTGCTGAGTC | 83860 |
rs146064916 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:7835181 | TGTCTTTGGCCACAC[A/G]TAAAATACACTAACA | 83860 |
rs146101962 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7838538 | AGGTGTGCACCACCA[C/T]GCCTGGCTAATTTTT | 83860 |
rs146103486 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920069 | TGGGCAACGTAGGGA[A/G]ACCCATTCTACAGAA | 83860 |
rs146170907 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7900112 | GCTTACACCGAATGG[C/T]ATAAAATCCACTGAC | 83860 |
rs146174337 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7995445 | ATAGGTTGCCATTTT[G/T]GTTTCCTTTTTATTA | 83860 |
rs146177742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972331 | TTCTGTATGTATATT[A/G]TTAGCATCCTCATTA | 83860 |
rs146188755 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7903429 | CCTTGGAAGCAACTC[C/T]TTCTCCAGGAAGCTC | 83860 |
rs146219491 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870359 | CAGATCCATCAGGAT[A/G]TGTTCTCTCCATTTT | 83860 |
rs146223631 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7860329 | AAATGAATTATTAAG[C/T]GTTTGAAAATTAGTT | 83860 |
rs146248273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952134 | ATAAATTTGATTTGC[A/G]CAAAGGGCCTACATC | 83860 |
rs146260567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8010168 | CATTTCTGCCTCCCA[A/G]CGTGCTGAGATGACA | 83860 |
rs146274463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969042 | TGGCCAGGTGCAGTG[G/T]CTCATGCTCCCAATA | 83860 |
rs146286595 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015502 | AAAACTCTTCAGACT[A/G]AAAGATTGCCCCTAA | 83860 |
rs146296115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992636 | TATGGAGTGAAATAA[C/T]GAATGCACATTTTCC | 83860 |
rs146310092 | snp | A/G/T | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7924658 | ATCCTTTAAAAATCT[A/G/T]TTCTTTTTTATTTTT | 83860 |
rs146342675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876973 | TCATCCTGATTTTCA[G/T]ATCTCTCTTTGAACT | 83860 |
rs146382060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7853648 | ATTAAACTAGAGGTC[A/G]GCAAACTGCCTGGCC | 83860 |
rs146406659 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7989139 | GGGCCTGGAAGTCCC[A/G]GAGCAAGCTCTCAGT | 83860 |
rs146414714 | in-del | -/A | 0.119281 | 0.213102 | intron-variant | TAF3 | GRCh38.p7 | 10:7851145 | ATTTTAAGGAGAAAT[-/A]AAAAATGCTAGAGTG | 83860 |
rs146426060 | in-del | -/GTT | 0.336017 | 0.234736 | intron-variant | TAF3 | GRCh38.p7 | 10:7874697 | ATATGTTTTGTCTTA[-/GTT]TTTTTTTTCAGTTAA | 83860 |
rs146457869 | in-del | -/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7909948 | TATGGCATAGTGATT[-/G]CATATAACCTATGCA | 83860 |
rs146465043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7985224 | CAGCTGATTAGACTT[A/G]CCTTTTGGGTTCCAA | 83860 |
rs146478556 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7928562 | TATCAATAATAATTA[C/T]TGTAATTCCTAGGTG | 83860 |
rs146478906 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7970415 | TTGAGAAAACTGCAC[A/G]GAAAGGTCGAGTACC | 83860 |
rs146500081 | in-del | -/G/TG/TTG | 0.621966 | 0.128559 | intron-variant | TAF3 | GRCh38.p7 | 10:7838366 | CAGTTTTGTTTTTTT[-/G/TG/TTG]TTGTTGTTGTTGTTT | 83860 |
rs146510566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852642 | TGGGGGTGTGTAACT[A/C]CGTCAGAGTACACAT | 83860 |
rs146513556 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7932429 | GTGTTTTTTACAGCA[A/G]ATATCCAAAGGTCAA | 83860 |
rs146587751 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8004631 | GATTTCATCATTGCT[A/C]ATTAAGAAGTCAGCT | 83860 |
rs146613991 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7989792 | CAGATGCAGAGAATG[A/G]TTGTTAGTTAGGTAA | 83860 |
rs146629461 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7869271 | TGTGTCTGTGTGTGT[G/T]TGTCTGTGTGTGTGT | 83860 |
rs146632746 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7951104 | GTGACCAGAGACTTA[C/T]AGGAACCTAACCGTG | 83860 |
rs146647718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827882 | GGATCAGTTGAGCCC[A/G]GGGGTCAAGGCTGCA | 83860 |
rs146647763 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7873026 | TAAAAACAAACAGAA[A/C]TCTTATTTCAAGACT | 83860 |
rs146652688 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7852058 | CAAAGCACTGGGATT[A/G]TAAGTCTGAGCCACC | 83860 |
rs146731896 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8007477 | GGGAAGGAAGTTCAT[C/T]TGAAACAAATATGGC | 83860 |
rs146734702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961610 | TTGTTTCTTCCTTGT[C/T]CATATCATCCATCAT | 83860 |
rs146750831 | in-del | -/TAAC | 0.345482 | 0.231048 | intron-variant | TAF3 | GRCh38.p7 | 10:7881192 | AGTGAGCCATGAGTA[-/TAAC]TAACACTGCACTCCA | 83860 |
rs146751009 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7893627 | TCCCGTAGCGAGATC[C/T]GTCCAAGTGTCTTCT | 83860 |
rs146755790 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939611 | CACACACACACACAC[-/CA]ACACACACACCTCTA | 83860 |
rs146770338 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7847290 | AACAAACAAGAAATA[C/T]GGTCTCTCATCTAGT | 83860 |
rs146775096 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7868438 | TGGAGGCAGTGTGAC[A/T]TAGCAGCCAAGCTCT | 83860 |
rs146808674 | in-del | -/GTC | 0.0744748 | 0.178019 | intron-variant | TAF3 | GRCh38.p7 | 10:7842807 | AAATTAGATATAAAT[-/GTC]GTATATTTTTACAGA | 83860 |
rs146819922 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7965968 | TTCATAGCCTAAGAG[G/T]CATCTAATCACAGAC | 83860 |
rs146865120 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7984348 | AAATACTTTTACTGC[A/G]CAGTAAAACAAGTGG | 83860 |
rs146891892 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TAF3 | GRCh38.p7 | 10:7865243 | GAGGCCGAGGCGGGC[A/G]GATCATGAGGTCAGG | 83860 |
rs146895503 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8008767 | CGCCACCTCTGAAGC[C/T]GTCAGAGCTTCTGCC | 83860 |
rs146905691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012984 | GGTTGGCTCTGTTCA[C/T]GTGAAGTTTGAGGAA | 83860 |
rs146913792 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7895902 | GCGCCTAGTTATCAC[A/G]TGACAGGAATCAAGT | 83860 |
rs146916243 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7967034 | TACACCTTGTTTTCT[C/T]CTCCTAACACACCTG | 83860 |
rs146918236 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7918907 | CTAGAAGCAAAATGA[A/G]GAGCAAGGAGGCACT | 83860 |
rs146928672 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7991045 | GCTGCAGTGACCTTC[C/T]CTTTTCTTTTTTTTC | 83860 |
rs146964743 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7874712 | GTTTTTTTTTTCAGT[C/T]AATTTTCTGTGGCCC | 83860 |
rs147020290 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913445 | CCTTTTCTCATAAGT[A/G]ATAGAAATAGAGAAG | 83860 |
rs147023924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936856 | CTCCCTCCCTGTACC[C/T]GCTGGCATCCATTGA | 83860 |
rs147035162 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7859451 | TTCAGTCCATTCCAG[A/G]TTGGGGGAGAATAGT | 83860 |
rs147054733 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817150 | TTGTGAAATCCAAGG[A/C]GCAAGAGAGTTTCAA | 83860 |
rs147108333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7971560 | CCTTTGCAGAAAGTC[C/T]CTGTCAAAAGATAAA | 83860 |
rs147116708 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TAF3 | GRCh38.p7 | 10:7975003 | CTCTTGAACCTGGGA[A/G]TTGGAGGTTGCAGTG | 83860 |
rs147124692 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7933990 | ACCGAAACCTGCAGA[A/G]TGAGTGTCAATGGCT | 83860 |
rs147178242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8003119 | ACTGAATCACTTAGA[C/T]CTTTTATGTGATATA | 83860 |
rs147181789 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7864532 | CAGATCTCTTGAAAT[C/G]TGTTCCTCCTATCTA | 83860 |
rs147183924 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7944661 | GGAATACAAAGGGTT[A/G]TCTCTTAGCTAATCC | 83860 |
rs147198353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7867638 | TATTTCAATATTGTG[G/T]AGACAGGATGGCTAC | 83860 |
rs147213291 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7949090 | CCATTACTTTTTTAT[C/T]GACTGCTCTTGATGA | 83860 |
rs147227664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825683 | TTCGTTGTGTGTTTC[A/G]TTGTGTGTTTAAGGC | 83860 |
rs147245401 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7849106 | TACATGTTTCCTTAG[C/G]TACCAAGTGCTTCAC | 83860 |
rs147285522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949415 | TATATAAGTGGACAC[A/G]AGAAGGGAGAGAATG | 83860 |
rs147290845 | in-del | -/A | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7844237 | TCTATTCAGAAATTT[-/A]AATTACTGTCCATTA | 83860 |
rs147305482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7889745 | CTTGTGAAATAGCCT[C/T]GTCTTGTGTCTTGTT | 83860 |
rs147320756 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7962443 | TTGTCTAAAATCCTT[C/G]TAGGTCCAAACTACC | 83860 |
rs147369555 | in-del | -/TTTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838929 | TTTTTTTTTGGTTTG[-/TTTGT]TTTGTTTTGTTTTGT | 83860 |
rs147378800 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7963585 | CGCCGCATGTTCTCA[C/T]TCATAAGTGGGAGTT | 83860 |
rs147391661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827069 | TCAGCCACTCAGCTT[G/T]GTTCATGTCAAAAAA | 83860 |
rs147394868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953043 | AGTGCCTGTTTTCCT[A/G]TTATTTCCTGACTGC | 83860 |
rs147394888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905329 | TTTCAGGGGAAGCCA[A/G]TGATTTTGACATTAG | 83860 |
rs147409731 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7830467 | CACCTTTTTCACTTT[A/C]CATGTCTTTTTTTTT | 83860 |
rs147411269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910026 | ATAACATAAATGCTA[C/T]GTAAATAGTTGTTAT | 83860 |
rs147413175 | snp | A/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817856 | GCTTACCTGTTTTTT[A/T]TAAAAAAAAAAAAAA | 83860 |
rs147433457 | in-del | -/TC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897645 | TCTCCTAGTTCCTAT[-/TC]TCTCTCTCTCTCTCT | 83860 |
rs147495664 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7982634 | CAAACTCCTAACCTC[C/T]GGTGATCCACCTGCC | 83860 |
rs147499758 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7925602 | TGAGGTCAGGAGCTC[A/G]AGACCAGCCTGGCCA | 83860 |
rs147500063 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7967372 | AGTGAAGCCATCAGA[A/T]TAGGTTTGTAACAGC | 83860 |
rs147512074 | in-del | -/GTT | 0.128632 | 0.218563 | intron-variant | TAF3 | GRCh38.p7 | 10:7849456 | CTGGGACGATTTAGG[-/GTT]GTTATTGCATGGGAT | 83860 |
rs147514406 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7850487 | TTGAGACCAGCCTGG[C/T]CAACATGGTGAAACC | 83860 |
rs147530484 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7930250 | TAAAAGGCCAGCAGT[A/T]ACATAAGCAAGATAC | 83860 |
rs147554826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7923082 | TTCTATATGAATAAA[C/T]AAAAGTCATTAAATA | 83860 |
rs147567774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995143 | GACTAAGGTTTTTTT[C/G]AGCATTTGCTCTTAA | 83860 |
rs147577504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8000152 | TTTTGTTTTTTGAGA[C/T]GGGGTCTCACTTTGT | 83860 |
rs147583378 | in-del | -/CTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826751 | GCTTGTCAAAACGTT[-/CTC]CTCTTCATAAGAAAA | 83860 |
rs147583866 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7874945 | ACTTTTTAGACTTCT[A/G]GTTTGGAATGTTGTG | 83860 |
rs147584596 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7926085 | AGAAAGGATTTTGTT[G/T]TTTATAAATATTGAA | 83860 |
rs147600328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879428 | GAACTATTTTTATTA[C/T]ACATGAAATGAAATA | 83860 |
rs147604088 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816739 | CAGGAGGATCCCTCA[A/G]TGAACTTTCTGCAGG | 83860 |
rs147620650 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7821552 | AGTTAAAGCAAGTAT[G/T]AGAAGTTACCATTAA | 83860 |
rs147660144 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7941371 | GGAAAAGTGATCAGC[A/T]GTTGTTGCTAGATAC | 83860 |
rs147672099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8012560 | ACACGTGGGAGCTTC[A/G]GGGCATAGGATGTTC | 83860 |
rs147681749 | snp | A/G | 0.0178098 | 0.0926698 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016585 | GGTTTTTGGAGAGGG[A/G]TGAGGGGTGGGGGAA | 83860 |
rs147687483 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817895 | TTTTATTGGAACCAG[A/G]GCTGGGATTAGAATG | 83860 |
rs147689710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7898967 | ACTTCAGGGTGACTG[A/G]GAATTGGCCTTTTCT | 83860 |
rs147689759 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7945609 | CCTCCTCCCACCCCT[A/G]CAGTAACTACCCACC | 83860 |
rs147703549 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7822219 | TAAGAATAGAGAGAA[A/C]GGAAAAAAATCTGAA | 83860 |
rs147705869 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7900909 | TCACAAAACAATTCA[C/T]GTTTAGGATACCATA | 83860 |
rs147758826 | in-del | -/G | 0.350546 | 0.22889 | intron-variant | TAF3 | GRCh38.p7 | 10:7831938 | CATTTGTATATATCT[-/G]GGGGGTGCAAAGCGA | 83860 |
rs147764880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7957684 | GAGTCCTTTTCTCCC[A/G]TTTCAGAACACTAAA | 83860 |
rs147792844 | snp | A/C | 0.0748431 | 0.178382 | intron-variant | TAF3 | GRCh38.p7 | 10:7837259 | TCCCAGCTACTCGGG[A/C]GGCTGAGGCAGGAGA | 83860 |
rs147794321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918121 | ACAGAGGCCTTGAGT[A/G]CATTGGCTGACTTGG | 83860 |
rs147794627 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7961053 | TCACCGTAAGACGAC[A/G]TGAGAGATGGTTCTG | 83860 |
rs147798256 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7922517 | ATTGCAAATTACAAC[A/G]TGCTGATTAATAAAG | 83860 |
rs147809071 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7839301 | ATAATTGCTGGTTTT[A/G]TTTGCCTCTGTAACT | 83860 |
rs147882904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974376 | ATTTCAGTGTGATGA[A/G]ATGAAATACTTATAG | 83860 |
rs147885067 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838920 | CTTGTTTTTTTTTTT[G/T]TTTGGTTTGTTTGTT | 83860 |
rs147892856 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978124 | ATAAAAATTCTACAA[A/C/T]CTTACTTTTCCCATT | 83860 |
rs147897949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858712 | CTTAGAACCGTGGCC[A/G]GGACATATTCACATG | 83860 |
rs147904111 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7939945 | TTTCAGAAGAAAAAC[A/G]TATAAATCTATATTA | 83860 |
rs147915599 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7862002 | GTCTTTATTCTGTCC[A/G]TTCTTCCAATTTGAT | 83860 |
rs147922278 | in-del | -/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842577 | ATGCGGGCTTAAAGC[-/TA]TATATATATATATTT | 83860 |
rs147956616 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:8013193 | AAGTTACTTAGTAAC[A/C]ACTCTTTTATATCCT | 83860 |
rs147979584 | in-del | -/G | 0.0360663 | 0.129354 | intron-variant | TAF3 | GRCh38.p7 | 10:7912352 | CGATCATTCTGCGTT[-/G]GCCCCGCAAAGCGCT | 83860 |
rs147988433 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7903503 | TTTTAATAAGGACAA[C/T]GGTGTTTAACTGTAT | 83860 |
rs148015524 | snp | A/G | 0.00202678 | 0.0317692 | intron-variant | TAF3 | GRCh38.p7 | 10:8013881 | CACTCATTAGGCAGC[A/G]TCAGCCGCTCCTGAG | 83860 |
rs148019459 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7832710 | GCCCACCACCACACC[C/T]GGCTAATTTTTGTGT | 83860 |
rs148056350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7881276 | AACCCACAAGCTCTT[C/T]TAATATACTGTTTTC | 83860 |
rs148059024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958058 | ATTTTACAGATTATT[A/G]GTAAATGATGATCAT | 83860 |
rs148064437 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7949044 | CCGCTGCTGACAGCC[A/G]CTCTCGGGTCAACAG | 83860 |
rs148073025 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7837702 | AGCCTGAGAGGCTGA[A/G]GTGGTGTAAGTACTC | 83860 |
rs148081044 | in-del | -/ATACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006178 | CTACTGAAAAAAAAA[-/ATACACACAC]ACACACACACACACA | 83860 |
rs148092509 | in-del | -/ATCTTTCCAGGTGTTCACTTTTTTTTTTAAACCTAGACTGA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900974 | TTGAAGTAGCGGTGT[lengthTooLong]ATGTAGATATTTATA | 83860 |
rs148095073 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7966812 | CAGTAATGGCAACTC[C/G]CATTTTTCGCCTACC | 83860 |
rs148100093 | in-del | -/GGTCCCTCGACCT | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7848543 | CAGCAACCCCTTCCA[-/GGTCCCTCGACCT]GGTCCCTCGACAGCT | 83860 |
rs148100590 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7956259 | CTTTGAGGGGCCGAG[A/G]TGGGCAGATCACGAG | 83860 |
rs148111564 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7929587 | GATTTTATAGACAAA[A/C]TCCTGGACTCAAGTG | 83860 |
rs148121191 | in-del | -/AACTT | 0.0704125 | 0.17392 | intron-variant | TAF3 | GRCh38.p7 | 10:7999859 | ATGGATGATGCACTC[-/AACTT]AGACGCACTCGATTG | 83860 |
rs148149216 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7971792 | TTTATCAGTTGGTGC[C/T]CTGAGGTGTGTGGCG | 83860 |
rs148273401 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875860 | TTAATCCAGAAGGCA[A/G]TAAAAGCAGCAAATT | 83860 |
rs148276118 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909377 | AACCATATTCACTAC[C/G]TCAGCACTTGGCCTC | 83860 |
rs148280860 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7981288 | TCACCCACCCTTGCC[C/T]TCGGGCAGTGGGTCC | 83860 |
rs148322473 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7888741 | GTTGACCAAGAAGAC[A/G]GTGACAGAGCTTTCG | 83860 |
rs148323366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7992107 | GGGACTACAGAAAGT[A/G]AAGTTTCATCCATGT | 83860 |
rs148329654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7953165 | TCAACATTCCATCAC[A/G]TTGTTTCACTTCGGT | 83860 |
rs148340538 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7829518 | AGGATTATTGGTTAG[A/G]TATATTGTCGGATGC | 83860 |
rs148343012 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7860024 | GCCTGTAATCCCAGC[A/G]GTTTGGGAGGCCAAG | 83860 |
rs148358394 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937677 | CCATCCTGAAGGATG[A/C]GTAACAGGTGAGAGG | 83860 |
rs148395240 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7825553 | CTCTCTGAATTTGTC[C/T]ATTCTAGGTACCTTT | 83860 |
rs148420898 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7880703 | CCTCATCTAGGTGGA[-/T]TTTTTTTTTAGTAGT | 83860 |
rs148424948 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7994524 | TTATTTATTGTTATT[A/T]AAAAAATAGAGATGA | 83860 |
rs148428507 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7891265 | TTCAGCCTTCATCTT[C/T]TATTGATTTATTTGC | 83860 |
rs148431996 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7845737 | TCAGCATCATTTTCA[A/G]TTGGCCGTGTGAGAG | 83860 |
rs148448912 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7830712 | TGGTCTGGAACTCCT[C/G]ACCTCAAGTGATCCG | 83860 |
rs148455951 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011398 | AGCTGGGACCACAGG[C/G/T]GTCTGCCACCACAAC | 83860 |
rs148469393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897894 | TTCAACTGCAGGGCC[A/G]AGCGATCCTCCCATC | 83860 |
rs148501618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950587 | TTTAAGTCAGTAGTC[C/T]GTAAAAGTACTGGAT | 83860 |
rs148535283 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7835038 | CGTACTTTCATTGTC[G/T]GGAGGGATGTTTTGC | 83860 |
rs148538084 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7914221 | TTCTATTAGAAATAC[A/G/T]TATGGAATTACTTAC | 83860 |
rs148562164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002655 | AGAAAAGAATGAATA[G/T]TCCGCACTGATTGAA | 83860 |
rs148567090 | in-del | -/CC | 0.324382 | 0.238678 | intron-variant | TAF3 | GRCh38.p7 | 10:7869245 | CCTTCCTGACTTCTA[-/CC]GTGTGTGTGTGTGTC | 83860 |
rs148574080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960223 | TCAGAATACCCTAAA[A/G]CTGTCTTCTTTCTGA | 83860 |
rs148622457 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7968612 | AAACACCATGCTAAG[C/T]ACTTTAATTCCTTAC | 83860 |
rs148625925 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7931422 | TACTATTTTCCCCTG[C/T]GATAGATTTTCCATG | 83860 |
rs148636815 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7851190 | GCAATTAAAAATATG[C/T]TAGTCAGGGGAACTA | 83860 |
rs148656435 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016342 | TTATGTGGTTAGAGA[A/G/T]ATGCGGTTTTCTGCC | 83860 |
rs148666046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7973491 | AAAAAGACTGCATTC[C/T]GTCTCAGTTTTGCTA | 83860 |
rs148673717 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7900669 | ACTATAGAAAAACTA[C/T]TTTTATAAAAATTTT | 83860 |
rs148709389 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7983752 | GCTGAGGCAAGAGGA[C/T]TGATTGAGCCTGGGA | 83860 |
rs148728547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945616 | CCACCCCTACAGTAA[C/G]TACCCACCCGGCTAC | 83860 |
rs148746707 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7871023 | ATAAGGAAAGACAAC[A/G]GAAAATTTTTAGTCT | 83860 |
rs148750011 | in-del | -/AAACAAAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969140 | GAGACTGTCTCTCCA[-/AAACAAAC]AAACAAACAAACAAA | 83860 |
rs148784139 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7925133 | CGAGTTTTCTGTGAA[C/T]CTTGGGATAAAAGTC | 83860 |
rs148794762 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7999392 | AAAAGGCAAGACCCA[A/T]AACTACGTACCAACC | 83860 |
rs148801102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7878055 | CCATGTGCCTCTGGC[A/G]TGCAAAATAATAGGG | 83860 |
rs148856076 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874273 | GCATTTAAACTTGTA[C/T]TGATGAAGTTTTAGA | 83860 |
rs148892779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927649 | CCCAGAATCTTTTCA[C/G]ACCCTACTTCATAAA | 83860 |
rs148895542 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948065 | ACTTTATGACTCTGA[-/T]ATTTTTTTTTTTTTT | 83860 |
rs148909300 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | TAF3 | GRCh38.p7 | 10:7880511 | GAGAAGTGAGCCACA[A/G]TTAAGTAACAGAAAC | 83860 |
rs148936781 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7827649 | GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAGTCCC | 83860 |
rs148940697 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008085 | CTGCAGCCCGTCTGG[C/G]AACAATCTTTTTTTT | 83860 |
rs148944295 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894268 | ACGGAGTTACTGTCA[G/T]CAGGGACAGTCGGCC | 83860 |
rs148946610 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7966325 | CACATTTCTGAGTAT[C/T]TAGGCTGATCTGGCA | 83860 |
rs148949425 | in-del | -/C | 0.030278 | 0.119257 | intron-variant | TAF3 | GRCh38.p7 | 10:7882662 | TAAAGGTGGAGTGCT[-/C]CTATCAGAAGGCAGT | 83860 |
rs148975571 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7954627 | CCAGTTAACACAGAG[C/T]TCTCCATAGTGAGAT | 83860 |
rs148989649 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7832039 | CTATCGTTTTTTGTG[C/G]AGAGAACATTTAAAA | 83860 |
rs148991875 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8013451 | AGGTCATATTGTTCA[C/T]AGAGATGATTATAAA | 83860 |
rs148993745 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7942035 | GGTCAGTTTTTTTGC[C/T]TCACAAGTGGGGTTG | 83860 |
rs149002253 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907402 | GGGCATTTAGATTTA[-/T]TTTTTTGTATTTAAT | 83860 |
rs149027381 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7923112 | ATAAGCAACTGTATT[C/T]ACATTCTACTATGAG | 83860 |
rs149061687 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011429 | GGCTGTTTCTTGGCT[-/G]GTTTTTGTTTGTTTG | 83860 |
rs149084170 | in-del | -/GTTTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902656 | GGTGTCTATCGGATG[-/GTTTTT]TTTTTCATGTAAAGG | 83860 |
rs149102453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961309 | TCGCGAATCGGTAGC[A/G]TAATTGATGAGGTTG | 83860 |
rs149114874 | in-del | -/ATA | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7963206 | TACCTGTCATTCCTG[-/ATA]ATAATAATAATCCAT | 83860 |
rs149116097 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7841381 | TAGAGCTTACAGTCT[A/G]CTTGGGGAAAGAAGG | 83860 |
rs149138488 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970799 | TATTAAATTTAAACG[A/G]TTTGTTCTTTAGAGA | 83860 |
rs149146741 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7864930 | TTCTAGAAGTTTTAT[A/T]GTTTTAGGTTTTGGG | 83860 |
rs149153127 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7853608 | ACGTGAAATTCTCAC[A/C]TACCCCTTCCTTGTT | 83860 |
rs149155274 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7933269 | TCACTGAACATACAA[C/G]TGTTTACATGAATTA | 83860 |
rs149163336 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7822425 | TACATTCAGTAAGAA[A/G]AAGAGTATTCGTTTT | 83860 |
rs149200975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869293 | TGTGTGTGTGGAGTG[C/G]AGGCAGGAGTGTAGA | 83860 |
rs149203529 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7902169 | GTTTGGACATATCCA[A/G]TCCCAGCACTTTGGG | 83860 |
rs149204062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7975417 | AACAGGCACTAGAAA[A/G]TAGCAGTAAGCAAAA | 83860 |
rs149245546 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7947796 | AGGAAGCACTGGAGG[C/T]TTTTGAGCAGGGAAA | 83860 |
rs149259001 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7824936 | CTTATTATTCAGGCC[A/G]TGAGTTGAATGCCAT | 83860 |
rs149276226 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8006059 | ACAAGGCCGGGCACC[A/G]TGGCTTACGCCTGTA | 83860 |
rs149286394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991812 | AATTTTAATATATTT[C/T]GAAGTGGTAATGTTG | 83860 |
rs149307379 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977412 | GAATTCCACAAGCTT[C/T]TCCCAGGTATGAACC | 83860 |
rs149309407 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7870728 | AAGTCCTTTCCTTGA[A/G]TGTCTTAACACTCAT | 83860 |
rs149400409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890006 | CTGAAACAGAAATCT[A/G]TTTGGTTACTGCTGT | 83860 |
rs149420541 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7899483 | GCATTTCTCTTTGCA[A/G]TGTTTCTTTCCCTCT | 83860 |
rs149470211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909213 | ATAACCCATTCTAGG[C/T]TTACTGGATCAGAGC | 83860 |
rs149475418 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7896862 | AAGTCAGATGTCAGC[C/T]CAGTCGAGCCCAGAT | 83860 |
rs149506987 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7956175 | CAACTTTTCTACGTT[A/T]GAAATTATTTCAAAT | 83860 |
rs149512455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944600 | TTAGTGCATCTTTCA[A/G]ATGTACCATAGTTAT | 83860 |
rs149518486 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016108 | TTTAATGTTAAAAAA[A/C]CATCAAATTTAACTT | 83860 |
rs149521458 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7834675 | TAAATACTGTCATCC[A/G]TACTGAGAATTCTGG | 83860 |
rs149558943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924714 | TTGAAAAAGAAAAAC[A/G]CTCATAATCTCACCA | 83860 |
rs149629966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7859855 | GTTGGACAAATGGCC[A/G]TTTCCCAGATAACTT | 83860 |
rs149633801 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7962410 | TTTCCCAACACATAC[C/T]CCACACGTTTTTCTC | 83860 |
rs149664091 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846745 | TCATATTTCCTGCAT[C/T]TTGAAACATTTTACT | 83860 |
rs149665570 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7926813 | AGTAAGCAATAGTTT[C/T]TAAACTTTGCTGCTA | 83860 |
rs149693134 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878705 | AATGTATGTATGTAT[C/G]TATGTATGTATGTAT | 83860 |
rs149736497 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7861282 | ACGGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG | 83860 |
rs149752322 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7939469 | ATGTAGAGTGTCCAG[C/T]GACTCACGCTTAAAC | 83860 |
rs149754469 | snp | C/T | 0.0153977 | 0.0863816 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964581 | CAGTAAAGAGACTAT[C/T]CAGGTAAAACAAATA | 83860 |
rs149773235 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7868189 | TATTGTTTGACAAGC[A/G]AGATGTTCTGAAATA | 83860 |
rs149775203 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7950443 | TGAATTAAACTCAAA[C/T]ATGTCCTAATTTGGA | 83860 |
rs149800577 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8007876 | AGTAATCCAAGGCCA[C/T]AGGTCTAGTCTCTGG | 83860 |
rs149807395 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7935946 | GCCCTGCGTGGAGGA[A/G]TAGAGCACTCTCGAG | 83860 |
rs149823650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7922377 | TTTTCCATTGTGAAT[A/G]TTGTACTGTCTTAAT | 83860 |
rs149827269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7874066 | GGTAATAGTAAGTGC[A/G]TTGAAGATATTATTG | 83860 |
rs149865430 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7961217 | GCTGTCAATTCAGAT[C/T]TGGCGGAGAAGATGG | 83860 |
rs149875847 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7887173 | GGAGGTGGAGCTTGC[A/G]GTGAGCCGAGATCGC | 83860 |
rs149946202 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7900824 | GAAGGTAAAGATTTT[-/G]ATTAGAAGCACATGG | 83860 |
rs149985123 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7911243 | AGGAAGGGACTGAGT[A/G]TTCAAACCCATGAGG | 83860 |
rs149990065 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:8011920 | TGGTGTCTCACGCCT[A/G]TAATCCCAGCACTTT | 83860 |
rs149992156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983041 | AAAACAGCAGGGGTG[C/G]ATGTGACTTCGGCGG | 83860 |
rs150019476 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7970466 | AGGGGGCCCAGGCCT[C/G]TCTGCCCGAGGCCTG | 83860 |
rs150032261 | in-del | -/AAG | 0.437824 | 0.164991 | intron-variant | TAF3 | GRCh38.p7 | 10:7888510 | GCATGAGATCTTCTA[-/AAG]AAGATGTGGAGGTCT | 83860 |
rs150035409 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TAF3 | GRCh38.p7 | 10:7957383 | GTTTTACAGAGATCA[C/T]GGGGAGGAGAATTGT | 83860 |
rs150063027 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871229 | AGACTTGCATATGTG[G/T]TAGAATTTCTACTTC | 83860 |
rs150065699 | in-del | -/GTTAAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857780 | TAAGTGATGTTTTTG[-/GTTAAG]TTAAGAAAGAAAAAG | 83860 |
rs150092763 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7912735 | TATTTCCCTACAAAT[A/C]CAGATCCAGTTCAAT | 83860 |
rs150107370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7985271 | CACGGCTTGTCGTCC[A/C]GGCTCTAGGAAAGAG | 83860 |
rs150121599 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7866500 | GCTAGACAGAGAAGA[A/G]TGAGCGCAAAACCTC | 83860 |
rs150129459 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | TAF3 | GRCh38.p7 | 10:7958906 | TTGGGAGGCTGAGGT[A/G]GGCGGATCACAAGGT | 83860 |
rs150138502 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7853565 | AACTGTTATCTGATT[C/G]AGCAAAGAAGTTGCT | 83860 |
rs150146136 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7919622 | AAATGCTCAAGTCCC[G/T]TATGTAAAATGGTAT | 83860 |
rs150182088 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7929846 | ATGTCCAGGCATGAC[A/G]AGAAAAGAGAACAGT | 83860 |
rs150190135 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818151 | AGGCAACACCAGCGC[A/C]GGTCTGCGTTTGGCG | 83860 |
rs150303047 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7951487 | TGTGGCAGTGGTTGC[A/G]GGTTTCCCAAGAGCA | 83860 |
rs150308180 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842176 | TTTGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 83860 |
rs150330949 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7829843 | TTGAAGGTGGAATAT[A/C]TGCATATGTTGTTAG | 83860 |
rs150346853 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7996402 | ACGTGGTTATTTTCA[A/C]CATGTGCTGCCAGCC | 83860 |
rs150354706 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7875958 | GTGATAGTAATCTTA[C/T]ATTACTATTAAACTT | 83860 |
rs150437058 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898788 | TTTTTGAAACTGTCT[G/T]ATTAAATTGTCTTTG | 83860 |
rs150483250 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:8005606 | AGACTTGCCTAATGC[A/G]TAAATGCCCTTGGGG | 83860 |
rs150491686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7901362 | TGCATGTTGGTCACT[C/T]TTTAAAATTCTTATA | 83860 |
rs150497972 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7861122 | ACCTGCCACTATGCC[C/T]GGCTAATTTTTTTTT | 83860 |
rs150534294 | in-del | -/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007609 | ATATATATATATATA[-/TA]CCTTTTTTTTTTAAT | 83860 |
rs150548375 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7971994 | ACTTTACCTCTTTGG[C/T]GAATTGGGAAGCTTA | 83860 |
rs150599868 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:8006805 | AATGAGGCCAGAGGC[C/T]GTCGTGAGCAACAGC | 83860 |
rs150601991 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7976617 | ACCATGTTGGCCAAA[C/G]TGATCTCGAATTCCT | 83860 |
rs150620474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7883064 | TCAAAATAAGGAAAT[C/T]AACATTGATACAATA | 83860 |
rs150631730 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7988220 | TAATCCCAGCACTGC[A/G]GGAGGATCGCTTGAG | 83860 |
rs150651162 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7867914 | TTTCGTATATTATAT[A/G]TACTATGTACTGTAT | 83860 |
rs150654964 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:7855292 | CCCTGGTTTGGTGCA[A/G]CTGAGCAGCTGCCTC | 83860 |
rs150658772 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7960603 | GAGTGTGACCACATA[C/T]TTGGGGATTGCAGAT | 83860 |
rs150687954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7921905 | CAGAGCTAAGGATAA[A/G]TCATATTTCTCTTAT | 83860 |
rs150718319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821122 | TCACTGCAGCTCTTC[A/T]GTGTAAACCTTGTTC | 83860 |
rs150725266 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8003714 | CCCTTCTCTAGTTAC[A/G]TATGCCTACATTAAA | 83860 |
rs150729079 | in-del | -/TGTTAT | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7845275 | CTGGAATATAACTGC[-/TGTTAT]TTTTTTGACGCCGCC | 83860 |
rs150756474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7938386 | GGGCAATGTGATGGG[C/T]GGGCCTCGCCTAAGG | 83860 |
rs150758246 | snp | A/G/T | 0.0751737 | 0.178706 | missense | TAF3 | GRCh38.p7 | 10:8009262 | CCCTCCCCGGGTCCC[A/G/T]CCGCCTCCGGGGCCA | 83860 |
rs150789295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981713 | ACAATTCAGTAACTT[C/T]ATCATCAGCCCTCGT | 83860 |
rs150789361 | in-del | -/T | 0.103438 | 0.202533 | intron-variant | TAF3 | GRCh38.p7 | 10:7851509 | TCATGTTAAAACAAC[-/T]TTTTTTTTTATCATA | 83860 |
rs150806276 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7834470 | TCAAGTACACAGTCT[C/T]GGTGCTAAGGGATAC | 83860 |
rs150807536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7864257 | TCCCTTACCCCAACC[C/T]GTGGCAACTACTGAT | 83860 |
rs150810161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943659 | GTAGGTGCTCAGTAC[A/G]CATTAAATGCATCAT | 83860 |
rs150811554 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7889270 | TCTCACTCTCCACAT[C/T]TGGGGAATGATCTCA | 83860 |
rs150828027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7842971 | GCAATAATATCCTCC[A/G]GAATTCTTTCTAATC | 83860 |
rs150846208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7953846 | AGAGTGCACGCCATA[A/G]GCAAATGAGTGGATT | 83860 |
rs150861012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7830866 | GAAATCTGGGTTGTT[C/T]GATCTGCAGAGTGCC | 83860 |
rs150863179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7910579 | AGAGGCAGGGTTTCA[C/G]CATGTTGGCCAGGCT | 83860 |
rs150866109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7896092 | TGAAGTAACTGCATC[A/G]GTTGCTGCTGATAGG | 83860 |
rs150871934 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7999515 | AGGCTGGAGTGCAAA[A/G]GTGTGATCTTGGCTC | 83860 |
rs150898752 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7878795 | GTGGAGCGGCATGAT[C/T]GGGGCTCACTGCAAC | 83860 |
rs150900765 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7956968 | GTGTCTTTTTTCTAC[A/T]AGAACTATAGGGGTT | 83860 |
rs150921018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7892843 | TTTTTTTGAGACGGA[A/G]TTTCTCTCTTGTAGC | 83860 |
rs150923661 | snp | C/T | 1.73688e-05 | 0.00294688 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964500 | GGTCACGACTCACAT[C/T]CCCCAAACACCTGTG | 83860 |
rs150937201 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7846119 | GCCCGCCACCACGCC[C/T]AGCTAATTTTTTGTG | 83860 |
rs150958523 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7912357 | ATTCTGCGTTGGCCC[C/T]GCAAAGCGCTGGAAT | 83860 |
rs150988399 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000596 | ACATAGCAAAACCCC[A/C/G]TCTCTACACACAAAA | 83860 |
rs151027226 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7862865 | ATTTTGCAAATATCC[A/G]TAAGTTACTCCTTTT | 83860 |
rs151074644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7973795 | AGACTGGACCATTTG[C/T]TTTCAGATTTGTTTA | 83860 |
rs151093132 | in-del | -/TTTTG | 0.350109 | 0.229081 | intron-variant | TAF3 | GRCh38.p7 | 10:7826445 | ACAATTTAGTGTTTT[-/TTTTG]TTTTGTTTTGTGTTG | 83860 |
rs151095097 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7839163 | TGATGTTTCCCAAAA[A/G]TAACTATGTACCTGG | 83860 |
rs151103372 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838921 | TTGTTTTTTTTTTTT[G/T]TTGGTTTGTTTGTTT | 83860 |
rs151116556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907096 | GGATTGAATAACTTA[C/T]AGCAATTTTTGTAAA | 83860 |
rs151127180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978876 | TAGAGGAATAAGATT[C/T]GTTAAAAGGCATTGA | 83860 |
rs151134071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7932119 | TAGAAATTTAACTCG[C/G]AGCATATTCAATACT | 83860 |
rs151153162 | in-del | -/A | 0.114387 | 0.210022 | intron-variant | TAF3 | GRCh38.p7 | 10:7843193 | GCTTACTGCAGCCTC[-/A]AATTCCCAGACTCAA | 83860 |
rs151157437 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7990492 | TTTTGAATGACCGCT[A/G]CATCTTTTTTCTCGC | 83860 |
rs151164265 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840158 | TTAGGAAAATGAGTG[-/T]GTTTTTTTTTTTTCG | 83860 |
rs151171780 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7951329 | TTGGCTCAGCCATGC[A/G]GCTCTTCTGCTGGAC | 83860 |
rs151187824 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7935795 | CCTTGAGGCTGAAGA[A/C]TTCTCATTGATTCAG | 83860 |
rs151193212 | in-del | -/T/TTTTTTTTTGGTGGTGGTTTGGGCTCCTTTTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834048 | CTTATATATTTTGCC[lengthTooLong]TTTTTTTTTGGTGGT | 83860 |
rs151238183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822605 | TTAACCATTGGCTGA[A/G]TATCCTTCCAGAGGT | 83860 |
rs151239622 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7901160 | CTGTCAATGATTTTA[A/T]TAAAGCTATTTGTAA | 83860 |
rs151324451 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994977 | TCCGTCTCAAAAAAA[A/G]AAAAAAAAAAAAAAA | 83860 |
rs151327639 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7946053 | TCCTGCCTTGGCCTC[C/G]TCTGTGGGGCTGAAG | 83860 |
rs151336254 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7836099 | CTCCTACTGCTAAAA[C/T]ATTGGTGCTTCTAAA | 83860 |
rs180726131 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7867437 | GTTTAAATTACAGCT[C/T]GCAAATATTTCCTGA | 83860 |
rs180731528 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7892650 | CTGCTGTAAAGTTTG[C/G]GTTGGTTTTTGAAAC | 83860 |
rs180736845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876678 | ACTTGAAAATACAGC[C/T]ATATTGTCCTAAAAG | 83860 |
rs180739782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7911462 | AAGCAGACCCAAAGG[A/G]AATAAAGTAATGCAT | 83860 |
rs180752858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7990994 | CAAAGCAGCTCTCAG[A/G]TGCCTTCAACCCTTT | 83860 |
rs180763386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822276 | GTGGCCGAAGGGGAC[A/G]GGGACAGGGTTAGAA | 83860 |
rs180764000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8011522 | CTCAAGCAGTCCTTC[C/T]ACCTTGGCCTCCCAA | 83860 |
rs180767257 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7858833 | GTGTGTGTGTGCGCG[C/T]GCCTGCATGTCACTG | 83860 |
rs180774566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7933260 | AATGTCAGCTCACTG[A/C]ACATACAAGTGTTTA | 83860 |
rs180777538 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902774 | CATTTATTGATGATT[A/C]TTGTCAGTTATTATA | 83860 |
rs180781389 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7961624 | TTCATATCATCCATC[A/G]TGGTGACTTTAGTTA | 83860 |
rs180782746 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7841203 | ATTTGCTTCTTTTAC[A/G]GTGGTTATATACTGA | 83860 |
rs180783012 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7886131 | GGGGGGTCTCACTAT[C/G]TTGCCTGGGCTGGTC | 83860 |
rs180783331 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7924806 | AAACTTAAAGAAAAA[A/C]CCCTAGTTCTCTGGT | 83860 |
rs180785864 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950894 | TGAAGTCCTGTCTAG[A/T]GGTCCCAGTGCCAGA | 83860 |
rs180792396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943250 | GCTTGGTTTCTTGGC[C/T]TCTGTCTTCTGATTC | 83860 |
rs180798521 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7970170 | ATAATTGGGAGTTGT[C/T]GACAATGGAAAGCCC | 83860 |
rs180814689 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7981403 | GGTGACTGGTTGGGC[C/T]CCTCTAGACATCCCA | 83860 |
rs180837919 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8002330 | ATCCCGTCGCACATC[A/G]TAAAGCATATTATTA | 83860 |
rs180862869 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7906552 | TATGAAACCTTAGAG[A/G]TTTCTGCTAAGACAC | 83860 |
rs180865913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7937256 | TTTTGTAAGAAACTG[C/T]CAAACTGTCTTCCTA | 83860 |
rs180868183 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7872439 | TTGCCTATTAAAATA[C/T]AGGAAGTTATATTGC | 83860 |
rs180887312 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7987890 | ATCTCTTCTGAAATC[C/T]GTAGGTCCTTGGTGC | 83860 |
rs180895926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896361 | CTAATGCTGTCCTGT[G/T]CAACTACTCCCAGGA | 83860 |
rs180897735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7889020 | CTTTTTTTTTCTACA[C/T]GTGGGATATTGGAGC | 83860 |
rs180900517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7838859 | GAGTTCCAGGGTCTG[A/G]GGAACGTTCCTTCTG | 83860 |
rs180902905 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881462 | TCAAGTAAAAGACAT[A/T]TGTCTCTCAGACACA | 83860 |
rs180904132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008523 | TTAAGAAGAGAGAAA[C/T]AGAAACTTTTTCTTT | 83860 |
rs180906878 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916691 | TTAACTGCTTTAGCA[C/T]AACTTGATATTTAAG | 83860 |
rs180910392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862668 | GCCTTTTGCAATCCA[G/T]ATCTCCTCTTCCCTC | 83860 |
rs180922361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928309 | ACATAGGAAGTACTT[A/C]AGTATTTTTTGAGTG | 83860 |
rs180923566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7946929 | TTTTTAAAAAAATAA[C/T]TATTTGTTTGTTTTT | 83860 |
rs180924095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954793 | TTCAGAGTGCCCTCC[A/G]TAGGCGAATGAGTGA | 83860 |
rs180932918 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965346 | ACTTGTGAGGAAGGA[A/G]AAAGAGAAGCATAAA | 83860 |
rs180947902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973698 | ATTATAGGTAGCTTG[G/T]AAATGTTTGTTTATT | 83860 |
rs180952344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854769 | TTGTGAAGGACAGTA[A/G]GTATTCAGATCCATA | 83860 |
rs180962507 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015748 | AGGAAAACAAGGCAA[C/T]TTAAATTTAGAGTTT | 83860 |
rs180990706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995429 | TTATACTCCTTATTC[C/T]ATAGGTTGCCATTTT | 83860 |
rs181108902 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7956357 | CCAGACATAGTGGCA[C/T]GTGCCTATAATCCCA | 83860 |
rs181116902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8007445 | ACCTGTCTTAGGGCA[G/T]TGGTTGCTCTGGGGC | 83860 |
rs181120039 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7975119 | AAATAATTCGTGGAA[C/T]AGAAAGACTGAAGAT | 83860 |
rs181125214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996533 | TAAAAATCAGAAAGC[A/G]AAAATATGGAGATTA | 83860 |
rs181170821 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7840998 | GGGATTACAGGCACA[C/T]GCTGCCACACCTGGC | 83860 |
rs181174938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858494 | ACTGTTTTTTCACTA[C/G]TTCCGGATCTTACTG | 83860 |
rs181185383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7821828 | GGTAGGATTACTTCA[C/T]AGAAAAGATAAGATT | 83860 |
rs181239932 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7833633 | TTTCTTTTCAACATC[C/T]TGTTCTGTAGCTTCC | 83860 |
rs181274763 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7854558 | GTGAGGTAAAGCAAC[A/T]GGAAGAAGCCTGGGG | 83860 |
rs181293151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7838176 | GGTTTAGTTGACTCC[A/G]TTCAGTGCTGTGTGT | 83860 |
rs181294649 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7871898 | ATTTCTAATATTTGT[G/T]CATCACTTAAAATAA | 83860 |
rs181305154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819457 | TTTGTCAGTTTCGCT[G/T]ATTAGATGTACTTTC | 83860 |
rs181351224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888631 | GTGCATTTACAGGTT[A/C]TGTAAGTGCCCTCAC | 83860 |
rs181355876 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7927173 | ATACTCATCTTTCAT[A/G]TCCATGAGTTTAAAA | 83860 |
rs181359241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905282 | ACACGCGCTGCCTTG[A/G]CTATAAATAGCAAAG | 83860 |
rs181364117 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818426 | CGATCCCGAGGAATC[C/G]TTCCGCTCCCAAGGG | 83860 |
rs181371905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7837802 | CCAGCCTGGGTGACA[A/G]AGTGGGACCCTGTCT | 83860 |
rs181424709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946459 | CCAGGCACCATGGCT[C/T]ATGCCTGTAATCCCA | 83860 |
rs181427834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917776 | ATGAGGAAAGATGGG[A/C]ATGAAGAAGGAAATA | 83860 |
rs181442755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986818 | GGGAAAAAAGGATAT[A/G]TAGCTAGGATTTTAA | 83860 |
rs181489391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7863068 | AATAAGCTATGCTTT[A/G]TCTCTGACCTAGGAG | 83860 |
rs181496660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897167 | CGCTTGGCAAGTCTC[A/G]CTTGTGCATCATCAT | 83860 |
rs181502832 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7882029 | CGATTGGGCACCTAC[A/G]GTGAGTTCAAAACTG | 83860 |
rs181526540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974446 | TTGGCCTTAGTGTCA[A/G]TCAGTGCTAATCCAG | 83860 |
rs181529469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927029 | GTGGGGGATGAACAC[A/T]GAAAACGATAAGATC | 83860 |
rs181535796 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7853981 | GTTCTTTTTATTTGT[A/G]AATTATGTGCTGTGC | 83860 |
rs181539261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7917401 | CAGAAACCAGCTGTG[C/T]ATGAGAGGGAGTGAG | 83860 |
rs181548701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937888 | AGGTTAAATAAGGTA[C/T]GCAAGGTTGCATAAT | 83860 |
rs181551008 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7956020 | AGGGTAAAGGATCGT[A/G]ATGTCTACAACTTAT | 83860 |
rs181569658 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7888137 | ACACTCAGATCTCTC[C/G]CATATGAAACGTTTA | 83860 |
rs181572491 | snp | G/T | 4.98732e-05 | 0.00499341 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964692 | CTCTATCGATGCTGT[G/T]ATTGCACGAGCCTGT | 83860 |
rs181582036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938222 | CCTAACTTGAAGCAG[C/T]GGAGAGCCTTGGGAG | 83860 |
rs181639418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7971026 | ATGTTCCAAGAGAAA[A/C]CAAGAAACTTAATGT | 83860 |
rs181644007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904710 | GCTGGAACTGTGTAG[C/T]GTGCACAGCGTTGGC | 83860 |
rs181655206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995992 | TTGGCGTCTTAAGGA[C/G]TGGTACTCTAAATAT | 83860 |
rs181674859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7981281 | CATCTATTCACCCAC[C/T]CTTGCCCTCGGGCAG | 83860 |
rs181678177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8001788 | GATTTTTTTAATTAA[C/T]TATACCATCCAACAA | 83860 |
rs181696433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845391 | TGTCCTCCGTTTTTC[A/G]TTTAATTAAGTCACT | 83860 |
rs181703983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871329 | GTTCCTAAAACCAGA[C/T]ATTCTTACAGAAATA | 83860 |
rs181731019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902439 | AAAAAAAAATAATAA[A/T]AAAAGAATCTTTTCT | 83860 |
rs181734000 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867378 | TTAGTCATTTGTTTC[C/T]TCTAGAATTTTAATG | 83860 |
rs181740776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942924 | AGCTGTAGGCTGTCT[C/G]TGCAGGTCTTCTGCT | 83860 |
rs181764591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7867200 | GGAGGCAGAAGTTGC[A/G]GTGAGCCGAGATCAT | 83860 |
rs181796153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012591 | CACCAGCCTTGGCCT[C/T]TAGACAGCAGGTACG | 83860 |
rs181837947 | snp | A/C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016701 | GATCTGAAGTTGCCA[A/C/T]GTTTAAGTGAGCAGG | 83860 |
rs181893484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845317 | GTCTTTGTGTGTGTG[C/T]GTGTGTGTGTGCACA | 83860 |
rs181904682 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827459 | TGATACCAGCCTGGG[C/T]AACGTCATGAGACCT | 83860 |
rs181938890 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7923684 | CCTGATGGCAAAACT[G/T]TTTTGAAAAGAGTAC | 83860 |
rs181945659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991205 | CACACACACATATAC[A/G]TACATACACATCCGT | 83860 |
rs181999783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7841916 | AGCTCAGGATTGTAA[A/G]ACATGACACGAACCT | 83860 |
rs181999992 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866758 | CCTAGAAAGCCCAAT[G/T]AGAGGCGAGTGTTAG | 83860 |
rs182005854 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7849765 | GCTCACTGCAACCCC[C/T]GCCTCCCAGGCTCAA | 83860 |
rs182007862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7859645 | GAGGGAACAGGATAC[A/G]GTTCATCTGCCCATT | 83860 |
rs182010560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885296 | CACACACAAAGTGAC[A/T]AATTCCTTCCCCTAC | 83860 |
rs182015947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7884597 | TTCATCGTGTTGGCC[A/G]GGCTGGTCTCAAACT | 83860 |
rs182016024 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7823784 | GGATTACAGGCCTGC[A/G]CCACCACGCCCGGCT | 83860 |
rs182042443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991674 | TGTATATGTATGTGT[A/G]TGTCTATATCACATG | 83860 |
rs182047160 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7960752 | TTTATTTTTTCCTCC[A/C]ATTTCCCAGATGGAG | 83860 |
rs182050770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980490 | GGTGAGTCCAGGACC[A/T]CCTCCTGATAGTGTT | 83860 |
rs182064547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961179 | GGGAAAGCACATGAA[A/G]GCAAACAGAGTTGAA | 83860 |
rs182065443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922638 | TGTTGTACCCTGTCC[C/T]CATTTAAATAATAGG | 83860 |
rs182065587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877558 | AATGTAATGAGAATA[C/T]GGCATTTATTGTTAG | 83860 |
rs182078159 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7901648 | AGGTGTGCATTGAGC[A/G]CAGTTATTTTGTGTA | 83860 |
rs182082285 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7941760 | GCAGTGTTGAGGAAA[A/G]GGGCAGGGTTGTGGT | 83860 |
rs182084408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850097 | CCTCGTATTTCCTGA[C/T]AAGTCCTCTCTGTCT | 83860 |
rs182094170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834594 | GATAGGGTTCCTCCT[C/G]AGTTCATGCAGATTT | 83860 |
rs182216053 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883038 | GCTTCTCATATGTAA[C/T]AGAACAGTTATCAAA | 83860 |
rs182219376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865130 | AAGTGAGTGGGGCCT[A/G]GGGGTCAGGAGCTTC | 83860 |
rs182221515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970737 | ATTAAAAATTTTAAT[A/G]TTTCTTTATCCCCAA | 83860 |
rs182232218 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011739 | ACCTCCTTGACCTTC[A/G]TGTCTTCATCTGTAA | 83860 |
rs182233305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830552 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAACT | 83860 |
rs182253465 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7849074 | CTAGAATTAAACTTA[C/T]GAACCGCAACAACAC | 83860 |
rs182254339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8013102 | GAACCTTGTAGCTCT[A/G]TGGCCTCCCTATCCC | 83860 |
rs182263360 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7898421 | CATGATGGCGGGTGC[C/T]TGTAATCCCAGCTAC | 83860 |
rs182280900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952831 | TTTATTTTAAAAATA[C/T]ATACCCACTTACACA | 83860 |
rs182284217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7971836 | CTTGAAGATTAACAA[A/G]AAAAATGCAGCACAT | 83860 |
rs182292462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7993385 | GGTCTTGCTGTGTTG[C/T]CCAGGATGGTCTCAA | 83860 |
rs182293630 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7912762 | CAATGGTTCATTGCC[A/G]GTGGCTTAATCCGTC | 83860 |
rs182303186 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7951693 | CATTTTTACAGTCTG[A/C/G]CTCGTACTTCTCATA | 83860 |
rs182350766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7930164 | TGATTGTGGTACTGC[A/G]CTCCAACCTGGCAAC | 83860 |
rs182354239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819898 | CTTCCACAGGGCTGC[C/T]AAAATAATCTGTCCA | 83860 |
rs182355650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949408 | TGTCTTATATATAAG[A/T]GGACACAAGAAGGGA | 83860 |
rs182382372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8010382 | CTGTAAATGTAGAGA[C/T]GCATGGTGGTACTGA | 83860 |
rs182414815 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7824981 | AACAGTGAGTGAATC[A/G]TGAGTATTCAGTGAC | 83860 |
rs182419807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968185 | GCTTTATGTAAGGCA[C/T]CAAAGGTTAAACTAA | 83860 |
rs182422887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7989234 | TGATTGGCCTGGCTT[A/G]TATGTGTTGCTTGGA | 83860 |
rs182480574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894479 | CAAGTGTAGTGTGAT[A/G]CGTCAGTGACCTGAT | 83860 |
rs182486859 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7935503 | GCAGGAGAATGGCGT[A/G]AACCCGGGAGGCGGA | 83860 |
rs182505838 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7860779 | TTAGCTAACAGGAGC[C/G]TTTTCTTTCTTTCTT | 83860 |
rs182516191 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833335 | AGTGTACAAGGATTC[C/T]CCCTTTTCTCCACAT | 83860 |
rs182522649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929558 | GTGTGCCACCACACC[C/T]GGCTAATTTTTGTGA | 83860 |
rs182524932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908028 | GATTTGCTCAGCAGC[A/G]TATGGAATTCGCCCT | 83860 |
rs182530635 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7963290 | CGCACGTGTGCTTCT[A/G]TGTGCATGAGAGAGA | 83860 |
rs182538684 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7948230 | ACTGGGCCCTACTAA[A/T]TTTTTTTTTCTTTTC | 83860 |
rs182543318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004610 | ATGTTATTCCACTAT[C/T]TTCTAGATTTCATCA | 83860 |
rs182559032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934633 | TATTTTTAGTAGGGA[C/T]GGAGTTTCACCGTGT | 83860 |
rs182622496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908668 | CTATGCCACCAGAGC[C/T]ACAAAGCACATAATG | 83860 |
rs182625589 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7938958 | AAAATGTATAAAGCC[A/G]TAAGGATAATAGAGC | 83860 |
rs182636231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976560 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 83860 |
rs182670542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842812 | AGATATAAATGTCGT[A/G]TATTTTTACAGATCT | 83860 |
rs182736643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914428 | ACTTATAATCTGTCG[G/T]TAAGAGTATTTTGTT | 83860 |
rs182772219 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908438 | CTTTAAATTCTAACA[A/C]TTGCTATTTCATGTG | 83860 |
rs182779221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878657 | TAGCTTATAGGAAAT[G/T]CCCTCTCTAGATGCA | 83860 |
rs182789102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988454 | AATTACACCTGTTAT[C/G]CCAGCTACTCAGGAG | 83860 |
rs182803399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7883691 | CAGTTGGCATTCTAC[C/T]CTATGGAAGATTTTC | 83860 |
rs182805723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982948 | AGTGGAAACACTCCT[A/G]TTTCCTTTTCTGAAC | 83860 |
rs182809773 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873959 | GTTTCCCCTCGAGAG[A/G]CCATTGCAGGTTTTA | 83860 |
rs182813415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918935 | ACTCACCTCACCTCC[A/G]GACAGCTTGCTGCGT | 83860 |
rs182816554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899720 | TGATTTATGTATATG[A/G]TAGACTATTGAGTGC | 83860 |
rs182816886 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7856153 | TGCAGTCGAGAACTA[C/G]AAAATAAAGGTAAGG | 83860 |
rs182819872 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890773 | GTTTATTTTTAAGAT[A/G]CTTCCTCACACCTAC | 83860 |
rs182833475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839793 | TTTTTTACTGACAGC[A/G]TAAAGATTGAAGTAG | 83860 |
rs182853137 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7998181 | AAAAGTTTGTCTTGT[C/G]AACACTGAGTAGCCA | 83860 |
rs182866112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7939721 | AAAATATAATAACCA[A/G]AAGAAAATGTTCTAT | 83860 |
rs182879991 | snp | C/T | 0.0147231 | 0.0845269 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009249 | CCCTGCCCTGCTGCC[C/T]TCCCCGGGTCCCGCC | 83860 |
rs182881783 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957721 | GAAAATGAGTTCTTA[C/G]TTCTTTGGAAATAAA | 83860 |
rs182886376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7978520 | CACATTACTCTTTTC[A/G]GTTGTGCCAGTAGAG | 83860 |
rs182898646 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7839354 | TAAGTCCTACACTCA[A/T]TCTCCATTTCACCAT | 83860 |
rs182906333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957104 | CACTATCAACTTTAA[C/G]CAAACTTTAGCACAA | 83860 |
rs182916621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855678 | ACAGCTTTTTTAGTT[C/G]CATTCTAAAGGCTTA | 83860 |
rs182918763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820441 | ACTTATTGACTTTAC[A/G]TATTGAGTTCCAAAA | 83860 |
rs182947923 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7918665 | GCAAGCTGGGACCTC[C/T]GACCCAGGCACTCAG | 83860 |
rs182974661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996786 | CTGGGCTCAAGCTAT[C/T]CTCCCTTCTCAGTCT | 83860 |
rs183006079 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:8003952 | TATAGTTATTTTCAT[A/T]AAAAAAAATGTTATC | 83860 |
rs183045753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860453 | AAAAGTAACCCCTAC[A/G]CTTTTAGTGCACACA | 83860 |
rs183049007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893667 | CTTGCCAGTTCCTTC[A/T]TATCATCCCTTTGCT | 83860 |
rs183053399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7852229 | TGCTGGGATTACAGA[C/T]GCCTGGCACCTAGCT | 83860 |
rs183053965 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967720 | TGCTTAGTACCGTAT[C/T]TGACGCATAAATGTC | 83860 |
rs183056619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7836570 | TGAGCCACTGCACCC[A/G]GCCCATTTCCACATT | 83860 |
rs183056671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878182 | TCCTGATTTTGTGAG[C/G]CCTAAAGCTTGTACA | 83860 |
rs183062037 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7842266 | CCAACCTCTGCCTCC[C/T]GGGCTCAAGCAGTCC | 83860 |
rs183063594 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981739 | CTCGTCCTAACAAAG[A/G]TGCTGAGAATGTGAT | 83860 |
rs183068050 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8003214 | GTTTTTTTTCTCTCT[C/G]TCTCTTTTCTTTTAT | 83860 |
rs183085153 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8009975 | GGAGTGCAGTGGTAC[C/G]ATCTCGGCTCACTGC | 83860 |
rs183092551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894816 | TTGACTGAAGATGCC[G/T]CCAACTTTTGCTCTT | 83860 |
rs183092606 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943524 | ATTGTCCTTGCCAGT[C/T]CTGTTCTAGCTGCCA | 83860 |
rs183095464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962430 | ACGTTTTTCTCTGTT[G/T]TCTAAAATCCTTCTA | 83860 |
rs183108970 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914238 | ATGGAATTACTTACT[A/G]GTGAAATAATCTGAT | 83860 |
rs183113930 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7935148 | TGTGCGTGCTGGTGC[A/G]CGCCTGTAATCCCAG | 83860 |
rs183116007 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7952686 | CAGGTCACTGTGTAT[C/T]TAGGAATTTATAATG | 83860 |
rs183219615 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7882657 | GTGTCTAAAGGTGGA[A/G]TGCTCCTATCAGAAG | 83860 |
rs183221324 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820716 | CTCAGGCTTGTGTCA[A/G]ACTCCTGGGCTCAAG | 83860 |
rs183328020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928893 | AGGTTACACTGTGTA[A/G]TTGAAAGCATTGTGC | 83860 |
rs183346847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7965945 | AACACACTAGCAGAT[A/G]TTAAAAATTCATAGC | 83860 |
rs183366588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865352 | GGTATGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 83860 |
rs183368450 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7831137 | GAAATAACTTTATAA[A/G]AAAATCCTTTTCCTC | 83860 |
rs183372694 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828808 | GGAGGCCGAGGTGGG[C/T]GGATCACTTGAGGTC | 83860 |
rs183373349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890321 | AGGTACCAAGCCTAA[C/T]TGGATGCTCTTGGTA | 83860 |
rs183428617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898107 | CTATCAACCCTTCTG[C/T]ATCAACTGGTATGCT | 83860 |
rs183429471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7844093 | TGTTCATAATTTAGC[A/G]TCTCTGGAACTTTGT | 83860 |
rs183430667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925436 | TATGGAGGTGTTAAC[C/G]TCTTTTATAAACATG | 83860 |
rs183432110 | snp | C/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7903458 | TCACCTCCTTTTAGT[C/G]AGGAAATGGTATTTA | 83860 |
rs183435337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861238 | GGAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 83860 |
rs183438150 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863685 | CACATATATATATAT[A/G]CACACACATATATAT | 83860 |
rs183503155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943953 | GCTCATTATAATAGG[G/T]TTCTTTATACTTTGA | 83860 |
rs183527191 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7869198 | AGATAAGATAAAAGA[A/T]AGATGTCACATATAA | 83860 |
rs183527562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903988 | AGAGCAGATCTGGGT[C/T]AGGGTGTCTGAGAAG | 83860 |
rs183570493 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982543 | AGCTAGGATTTCAGG[C/T]ATGTGCCACCATGCC | 83860 |
rs183582381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7947830 | TCTGATTTGGGATTC[A/G]GAGTTGGAGAGTCAA | 83860 |
rs183596781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7873439 | AATTTGAGAGATGAA[C/T]GAGATGGTTGAGGAA | 83860 |
rs183604269 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7907375 | TGAGATAATTTTAGA[C/T]AAAAAACAAATGGGC | 83860 |
rs183610902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846249 | GGCATGAGCCACTGC[A/G]CCCGGCCAAAAGGAT | 83860 |
rs183646997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953299 | CCTTTACCCAAACAC[A/G]TAAATCAAGTGGTAG | 83860 |
rs183656661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7988327 | GGGCACAGTGGCTCA[C/T]GCTTATAATCCTAAC | 83860 |
rs183659978 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7994000 | AAGGGTTCTGTCTCT[C/T]TCTGTCTCTTTTTCT | 83860 |
rs183694937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869873 | TTTATAAACTATTTG[C/T]ACTTTTTCCATTATA | 83860 |
rs183710687 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7887405 | GTGTGGAAAGAACTT[C/T]TTGTGATTGCAAAGA | 83860 |
rs183717230 | snp | C/G/T | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7837311 | GAGGTTGCAGTGAGC[C/G/T]GAGATTGCACCACTG | 83860 |
rs183723028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7824744 | TACCAAGCCGAGTCA[C/T]GGTGTAATCAAGGTC | 83860 |
rs183725614 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7852853 | TATATGAAAAGCTGG[A/T]TGAATGCTTGATCCC | 83860 |
rs183732152 | snp | C/G | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817118 | ACACCCAGGGTGGCG[C/G]CGGTAGCGGGACAGA | 83860 |
rs183733832 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7926752 | TCTGAATTTGAGCCC[A/C]TTATATCTAAAATGA | 83860 |
rs183746563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962802 | GGGCTAGACATATCT[C/G]TTATTGCTGCACTAA | 83860 |
rs183762253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926841 | CTATTTAATCATGGG[C/T]AAATTTACTTTATCG | 83860 |
rs183766792 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7904045 | GAGTCCAGTGTACTT[A/G]GAAACAAGGGCCGCA | 83860 |
rs183769909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944233 | GTTGGATAAACATAC[G/T]GGAATACTGCCAAAA | 83860 |
rs183796147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011628 | TTCTAAAAGTGTGAT[A/C]ATCAAATTGGTCCAT | 83860 |
rs183804275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7892584 | TTAAACTGGTAAAAT[A/G]GAATATATTGTCAAA | 83860 |
rs183819061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7911075 | ATTTTGACTTTAATT[A/G]TATGATTTTTGAGGG | 83860 |
rs183836773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876364 | TGGGCCTGGTTTTCT[C/T]TAAAATTAATTAGGA | 83860 |
rs183843510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7858600 | TGTCTTAGATTATTA[A/G]CTAAGTTCAGTCTTT | 83860 |
rs183847594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7990265 | TTCTGAACGGAATGA[A/G]CAGAATGAGTAAATC | 83860 |
rs183848294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866339 | ATGAGAGATGAGGCT[G/T]AGTGCAATGCACAAG | 83860 |
rs183858301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901288 | GTTTCCAAACCTCTG[C/T]GTAGTCCATGCCACA | 83860 |
rs183862179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7884535 | AGGATTATAGGCGCC[C/T]GCCACCATGCCTGGC | 83860 |
rs183863811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7833276 | AGTTTTTGGAGGAAA[C/T]TCCACATAGTTTTCC | 83860 |
rs183868066 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7978915 | GTATGGTAGGCCATG[C/T]CTGTAGTCCCAGTTA | 83860 |
rs183871475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7972249 | TCTGTTTTTATTTTG[A/G]TGAGCACACAGATAA | 83860 |
rs183871865 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848148 | ATGGCTTAACAATAT[A/G]AAGGTTCCATTGGAG | 83860 |
rs183873833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7932505 | GAGAGATTGATTATG[A/G]GTCTGGGGTCATGTT | 83860 |
rs183875536 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950193 | ATTGCGACTCCTTAT[C/T]TTGGGGATGTAGAAT | 83860 |
rs183878604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000043 | GAATTAATTTTAAGT[G/T]TATAACTCAAGCCAT | 83860 |
rs183881383 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7969828 | CAGCCACACTGACCG[A/G]GGTGGAAATTCCAGC | 83860 |
rs183902201 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7936076 | TAGTGTGATTGTATC[A/G]TAAAACAGAGAGAAG | 83860 |
rs183903403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7921125 | TCTTTCTTTACTGCA[A/G]TGCCATATTATATAT | 83860 |
rs183938125 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:8014249 | TTTAGACCTCTTCAG[C/T]GGTTCCTAAAAACTG | 83860 |
rs184015494 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973276 | AATAGTAGAGCAGAA[G/T]TTTTTTAAAGGTAGG | 83860 |
rs184019324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995226 | AATTATTTTTGTTTC[A/T]ACATGGTTATGTCAT | 83860 |
rs184026459 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015097 | GCCTTTTCATTGAGG[C/T]ATTAGATGAGAAGAT | 83860 |
rs184050812 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887063 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 83860 |
rs184097070 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851899 | TAAGCAATCCTCCCA[C/T]CTCCTGAGTAGCTGA | 83860 |
rs184230577 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7862425 | AAGCTGTTTTTCCTA[A/T]GATGGGCAGCAGCAG | 83860 |
rs184233551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827176 | TGTGAGAGGCACAGC[A/G]TGGACCTCACGGCAT | 83860 |
rs184237522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868948 | TGAAGGTCTGACTCC[A/G]GAATTTATGCTTTTA | 83860 |
rs184241276 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7835732 | CAGAGGCCTGGTGGC[C/G]CTTTTGGGGTTTTCC | 83860 |
rs184249537 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858414 | CTCCTGGATGATACA[A/G]TCGTTTATGTCAGCT | 83860 |
rs184263483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840789 | TACTCATTGCCTTTT[A/G]TTTAGCTAATGACTG | 83860 |
rs184263873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875915 | TACGACTAATTTTAC[C/T]GACAGAAAATAATTG | 83860 |
rs184274825 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7821360 | CCCCTTTAAATCCTT[C/T]CTGTTGTTTTAACAA | 83860 |
rs184310777 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7936968 | AGTTTGACTTCTTTC[A/G]CTTACCAATATGCAT | 83860 |
rs184323943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831761 | ATTGGCTTTGGTGAC[A/G]TCCTCACCTTCTGGT | 83860 |
rs184344728 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7895948 | CGAAGCTGACCATGC[G/T]GGGGTGGAAATTCCA | 83860 |
rs184358480 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7844953 | GCATCAAATATCTTT[G/T]CACATGTTTTTCTTT | 83860 |
rs184362138 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840186 | GAGACGGAGTCTCAC[A/T]CTGTCACCCGGGCTG | 83860 |
rs184383288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854211 | GGATAATATATTCAA[A/G]GCTCATGAGAATTTA | 83860 |
rs184384729 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895107 | TGACCTTGGGTGATC[C/T]GCCTGCCTCGGCCTC | 83860 |
rs184390779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7879532 | GCATTATTTTAGAAA[A/G]CATTTAGAAATTTAT | 83860 |
rs184392475 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7915846 | TAGCTGGATTTGGTG[G/T]TGGGCACCTGTAATC | 83860 |
rs184398507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871686 | CAACCTCAGGTGATC[C/T]GCCCACCTCAGCCTC | 83860 |
rs184407393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819283 | CTAGTTGTCACAGGC[A/G]CTCCGTCTACCGGCC | 83860 |
rs184411846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837971 | TGTATGTAAAAGCAG[C/G]CATCAAATAATTTAT | 83860 |
rs184427422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994883 | GGGAGGCTGAGGCAT[A/G]AGAATCACTTGAACC | 83860 |
rs184433467 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:7954730 | AGTGCACTCCATAGG[C/T]GAATGAGTGGATTAG | 83860 |
rs184446641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7875546 | TCCTTCCAGAGCCAG[C/T]GGGCACGAAGGGGTT | 83860 |
rs184449057 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936332 | CAAAAGCTATAAAAT[A/G]TCATCCCTGGGAGCT | 83860 |
rs184451609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880209 | ACTCACTGCTCTCCA[G/T]CCTGGGTGACAGAGT | 83860 |
rs184455115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7954129 | ATAGGTGAATGAATG[A/G]ATTAGTCCCAGTTAA | 83860 |
rs184456692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979227 | CAGGTGCCTGTAGTC[C/T]CAGCTACTTGGGAGG | 83860 |
rs184463479 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7972949 | AGCTCCATGTAAGCC[A/G]TCAATATTACCAGAA | 83860 |
rs184469365 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916465 | GAATTCATTCTAAAA[A/G]TATGTCAGTGTATCT | 83860 |
rs184478468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820951 | GTGATAGGCTAGGCT[A/G]GGCTAGGCTAGGCAT | 83860 |
rs184491369 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922955 | ATTCTACACTTAAAC[A/C]GCTTAATAACATTAG | 83860 |
rs184493105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902222 | TGAGGTCGGGAGTTC[A/G]AGATCAGCCTGACCA | 83860 |
rs184493505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7941628 | TGGACATCCTTGCTG[C/T]GCCGATGCCTTCGAG | 83860 |
rs184509914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942007 | TTCAAGGAGTCAGGA[A/G]TATTTGTTTTGAGGT | 83860 |
rs184557553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7919824 | GGAACCCACACATAC[A/G]GAGGGCTGACTGTGT | 83860 |
rs184562471 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7857039 | CCAACTTTCATGTCC[A/G]TAAGCAAACCACTGT | 83860 |
rs184571965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958146 | TCACCTTTACCAGTG[A/G]TAGAGGCTAAACAGT | 83860 |
rs184578989 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7884287 | CATGTTGTCATTGTT[A/C]TTTGGACAGTCCCTT | 83860 |
rs184595510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000861 | TATATTCTTTCAAAC[A/T]TTTTTCTAAGTATAC | 83860 |
rs184629095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960043 | GTCCCCAGAGTTAGA[A/C]GAGCAGGATGCACCA | 83860 |
rs184690326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7940633 | CAGTTCTTGTAAAGT[A/G]GATAAGAAAAAAAGC | 83860 |
rs184718830 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865457 | GCACTCCAGCCTGGG[A/G]GACAGAGTGAGACTC | 83860 |
rs184727045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7841050 | GAGAGGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 83860 |
rs184729303 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7900797 | CTTTTTGCTCTTTAG[C/G]CTTCGTATTAAGAAG | 83860 |
rs184739285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7926901 | ACAATGTCAGAGAGA[A/G]GAGTATTTTACTGTT | 83860 |
rs184739359 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7945037 | CTACATAACTGTAGT[C/T]GTAATTTTTTACTCT | 83860 |
rs184743083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8011219 | CTCATGGTATTTGTT[A/G]TTATAAACTGTACAA | 83860 |
rs184793555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7963449 | CAATTTGTACATCTG[C/T]TGTTACTGACTGCCA | 83860 |
rs184796587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7984239 | TTTAGTTTTTACCCC[A/G]GCACAATACTGTTTA | 83860 |
rs184811992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005401 | GTGTGCCTGGGCACA[C/T]TGCAAGTCCAAATTA | 83860 |
rs184930492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7847483 | AGAGTCTTGCCCTGT[C/T]GTACAGGCTGGAGCG | 83860 |
rs184938501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821878 | TGGTTGTATAAAGGT[A/G]TAGAGTATTCCAGCT | 83860 |
rs184953499 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980649 | CACCTAGAGACAACA[C/T]ATCCAAGTGAATTGC | 83860 |
rs184957849 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8001296 | ACCAGGTGTTGTCAA[G/T]CTTTTTCATCTTTAC | 83860 |
rs185040995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7888857 | CCAGATTCAAGGCTC[C/T]AAGTAAAACTATTTG | 83860 |
rs185047141 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7845921 | TTGAAAAAGTTTGAT[G/T]TCTGAGTTTAAAAGG | 83860 |
rs185048991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927762 | CAATAGGTACCACCC[A/G]ACCAGATTTATAAAA | 83860 |
rs185050998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905574 | AAACATTGCAAAGCA[A/G]TATACTCCTTTAAAA | 83860 |
rs185063799 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7829487 | TTTCTTGTTTTTGAC[A/G]ACCTTGACAGTTTTG | 83860 |
rs185067519 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7871941 | TTTTAGCCAGATGAT[A/G]TATAGTGGGAAACCA | 83860 |
rs185078104 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7854568 | GCAACTGGAAGAAGC[C/G]TGGGGAGGAGGTAGA | 83860 |
rs185134582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968879 | TCAAATTGTTTTTCT[A/G]TTAGTGATGATAAAT | 83860 |
rs185156016 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7891662 | TTTGATTATGGTATA[A/T]GGCAGCTAATTTAAG | 83860 |
rs185166855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7931044 | AGTCTGTTGCCATCT[A/G]ATGCCAGTAAAAGCA | 83860 |
rs185177324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903206 | AGCCTGGGCAACAGA[A/G]CAAGACTCTATCTCA | 83860 |
rs185179423 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7886748 | ACACTTATAACATGA[C/G]CTCTGCCTTCAAGAG | 83860 |
rs185187440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925064 | AAATGTGTAGGGTAC[C/T]AAATTTCAACCCTTA | 83860 |
rs185190453 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7951364 | CTGGGATCACCCATA[C/T]ATTTACTGTTGGCTG | 83860 |
rs185190831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970362 | TTTAATTCTCCCAAC[A/G]GCTCTGAGGGTTTGG | 83860 |
rs185195474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7850334 | GTTTGGAGAAGCCAT[A/G]TGTCAGAGGCAAAAG | 83860 |
rs185209933 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7834666 | TTACATCCATAAATA[C/G]TGTCATCCATACTGA | 83860 |
rs185213917 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867896 | ACGGTCGATTAACAC[A/G]TATTTCGTATATTAT | 83860 |
rs185233799 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7949900 | GTGACTGCGCATCAC[C/T]ACTGCCTGTCCAATA | 83860 |
rs185244451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943382 | CATTTGGAGGGTGTT[G/T]TTTGTATTTGCCTTC | 83860 |
rs185257938 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7989693 | TTCTGGAGATTCTGA[C/T]CTACCAATATTTCCC | 83860 |
rs185264630 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7910154 | ACAGCCTGTAGGTAG[C/G]GTACAGAGGCCAGTT | 83860 |
rs185272752 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7945938 | TTGTTTGTTAACCTC[C/T]GCATTGCCAGGCGGA | 83860 |
rs185273930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7849920 | TCCTGAGCTCGGGCA[A/G]TCTACTCACCTTGGC | 83860 |
rs185275554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884920 | CTCACTATCTGTGTA[A/C]TTCTAGAATATACAG | 83860 |
rs185281692 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014827 | AAGGGAGCTGGTGCA[A/G]GTCTGCCGTCACATC | 83860 |
rs185289933 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985362 | GCTGGAACTTCGTTC[C/T]CTCTCTTAGCTCCTC | 83860 |
rs185298179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7905011 | GAGGAAAAGTGAAAC[A/G]TTTCTTGTATCCGTG | 83860 |
rs185304200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834179 | TCTGCTGTTTCCTTT[A/G]TTGTGCCAAAGCTTT | 83860 |
rs185374142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826267 | CTAGGACTTTGATCA[G/T]AATCTACACTTAACT | 83860 |
rs185379970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7861623 | TTTACAGATATTTTT[C/T]CACCATCTCATAACC | 83860 |
rs185392950 | snp | A/G | 6.67178e-05 | 0.00577533 | missense | TAF3 | GRCh38.p7 | 10:7964396 | TCACCAGCAATGGTC[A/G]GAAGTCCTATTCGAT | 83860 |
rs185398853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853420 | TGGCATGATTTATTG[C/T]CTTTTTTATTGTCTA | 83860 |
rs185402884 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7887798 | GTTTATTAAAATCCT[C/T]TATAATTTTAATTGG | 83860 |
rs185420575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888176 | CCTGAACGCTGTCTT[C/T]CTCTAGGCCAGGATC | 83860 |
rs185423481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995656 | CTTCATGCAATTTGT[C/T]TCATTTTTCAAATAG | 83860 |
rs185438393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7927035 | GATGAACACAGAAAA[C/T]GATAAGATCATGACA | 83860 |
rs185455058 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7955085 | GAATGAATGAATTTT[A/G]GTGGCATTGAGTCAC | 83860 |
rs185466198 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:8006593 | TCCAAGTTAGGAAGA[C/T]GATCACCCTTGCAGG | 83860 |
rs185499205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904355 | GTAGCCCTAATACAA[A/C]TGAAATGAAATGATC | 83860 |
rs185510289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7946543 | AGCCTGGGCGACGTG[C/G]CCAAACCTCGTCTGT | 83860 |
rs185510627 | snp | A/T | 1.66101e-05 | 0.0028818 | missense | TAF3 | GRCh38.p7 | 10:7964894 | ACCTCAAGTTCCGAT[A/T]ACTCATGGACAATGG | 83860 |
rs185535777 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7870680 | GGCAGAACTCGACAC[A/G]CTTCTGAGTTCGCCT | 83860 |
rs185541810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974107 | ATCTCCAGCCTGGGC[A/G]ACAGAGTGAGATTCC | 83860 |
rs185557476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914274 | AGATTTGTGTTAAAC[A/G]ATGTCGGGGTAAGAG | 83860 |
rs185560241 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015789 | GTTGTTTTGTTTGTT[A/G]TCTATTTTGTTTTTG | 83860 |
rs185572827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935380 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 83860 |
rs185576676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7952688 | GGTCACTGTGTATCT[A/G]GGAATTTATAATGCA | 83860 |
rs185580121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937506 | GGTAAAGTGTCTGTT[C/T]AGGTCTTTTGCCCAT | 83860 |
rs185584204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010698 | GATCACTTGAGGTCA[A/G]GAGTTCGAGACCAGC | 83860 |
rs185599233 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7893775 | ACCTCTGTTTTGCCC[A/G]TATCAATATTTTATC | 83860 |
rs185605540 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7878297 | AATAGATTGTGAAAT[A/G]TTATATAGCAATGAA | 83860 |
rs185605747 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012708 | AAGTTTTCCTGTCAA[C/T]GTAGTTTGCCTTTGT | 83860 |
rs185642261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7971408 | GGAATCTGAACTAGC[A/G]CTTGCTAAATTTGCT | 83860 |
rs185648579 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992843 | TGGATAGATTTAACA[G/T]TTATCAAAATGTTGC | 83860 |
rs185726725 | snp | A/T | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817955 | GATTTGGATTTTTTT[A/T]AAAAAACTGTTAAAA | 83860 |
rs185728084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7996612 | GATTGTGACATTTCA[A/G]TGTCTTTTTTTTTTG | 83860 |
rs185842876 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837471 | AGCATGGCGAAACCT[C/G/T]GTCTCTACTAAAAAT | 83860 |
rs185928993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864588 | CAGGTTTCTGTGTAG[A/G]CTCGTGTTTTCATTT | 83860 |
rs185947665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7838212 | TACCTGCCATGAGTC[A/G]GATCCTACACAAGGA | 83860 |
rs185991519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819703 | CATTGTATGTGTGTT[C/T]GTTGAGGAGAGGAAA | 83860 |
rs186029606 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7841218 | GGTGGTTATATACTG[A/G]TGGTGTGCCATTGGT | 83860 |
rs186051027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877856 | CTCTCCTTCTAGTAC[C/T]GTTTATACACCGTGT | 83860 |
rs186053558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7882780 | GGTAATACACCTGGG[C/T]TTTATTTTTTCCTTT | 83860 |
rs186057067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859680 | TGTATTCCACTTTTC[C/T]GCCGGGGCATTATGG | 83860 |
rs186067344 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7893170 | ACTTTAACATACAGT[C/G]TTTGAGTATTTGGGA | 83860 |
rs186074146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842067 | TGGGAGGCAGAGGCC[C/T]TCCTATCGTTCATTG | 83860 |
rs186084096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7876957 | AATCTAAATAAAACT[A/G]TCATCCTGATTTTCA | 83860 |
rs186088630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7823901 | GCCTCTCAGTGCTGG[A/G]ATTACAGGCGTGAGC | 83860 |
rs186094226 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7912314 | GATGTTGCCCAAGCT[G/T]GTCTCAAAATCCTGG | 83860 |
rs186117561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946951 | TTTGTTTTTGGAGGC[A/G]GATTCTCGCTACACT | 83860 |
rs186133428 | snp | A/C/G/T | 0.000266327 | 0.0115367 | missense | TAF3 | GRCh38.p7 | 10:7965467 | AAAGCCCCAGCACCC[A/C/G/T]CACTGGTGTTGCCCC | 83860 |
rs186151834 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859090 | ACACGGTGAAACCCC[G/T]TCTCTACTAAAAATA | 83860 |
rs186152018 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822462 | TTTCTTTTTTTAATG[A/C]ATCACAGAAGTAACC | 83860 |
rs186152429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981509 | GCCTTTCAGAGAACA[A/G]TATTATTATCAATGG | 83860 |
rs186166698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885698 | CCACACAGTCTTCAT[C/T]ATCTCCCAAATAATC | 83860 |
rs186185124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7933960 | TGACATGGTCGTCAC[C/T]GCCTGCACACATGCA | 83860 |
rs186188873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7987912 | CCTTGGTGCTGGCTC[C/T]GTCTCAGGTGAGTTT | 83860 |
rs186191341 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7917522 | TGGGGCCTTATAGGC[C/G]ATGATATGGAATGGA | 83860 |
rs186197495 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7897267 | CCAGGTCGCCGGGGG[A/G]TCACTTTTATCATTC | 83860 |
rs186204013 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7937980 | TTTATATTGAGGGCC[G/T]CTTAGAGGGGATTTT | 83860 |
rs186214011 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961242 | AGATGGGAGAGAATC[C/T]AGAATGACCCCAGGT | 83860 |
rs186230234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7892685 | TGTTTCTTAGAAAAA[C/T]TCCAACAGTATTTTT | 83860 |
rs186233322 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TAF3 | GRCh38.p7 | 10:7860503 | TGAGTGTATTTGTAC[A/G]TTTTATGGAATTATT | 83860 |
rs186240088 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:8002577 | AATCTGTGTACAAAC[G/T]ATTCAAATTGTTTTT | 83860 |
rs186249519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924209 | AAAGTGTGAGGGAGA[A/G]ATGGAAAGCCAAAAC | 83860 |
rs186249991 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867543 | AGTTCTGGAGGGTGT[A/G]TAGAATATAAGGAAG | 83860 |
rs186265997 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7956086 | AATTATATTAATAGA[A/T]GTAGTTATATAATAC | 83860 |
rs186270459 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962594 | TTTCTGTTTCTCTTA[C/G]ACTCCCCGTGTTTCA | 83860 |
rs186275066 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974798 | AGTGAGATGAAGGCC[A/G]GGCACAGTGGCTCAC | 83860 |
rs186277561 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:8001934 | TCCACTATAACAGCC[A/G]GCAAACAGTAAAGTT | 83860 |
rs186278686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961659 | AACAACACTCTTTCT[C/T]TCATGCACTCTGTCC | 83860 |
rs186283311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996210 | CAAGCTGGTGACTGG[G/T]ACCATAGGCATCCAG | 83860 |
rs186286550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881564 | AGCTGGAACGTAATA[A/C]GTTTTTTATATCAAA | 83860 |
rs186290257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862798 | TACTGTTTTTTGGTC[C/T]GGCCTTTTTTCACCA | 83860 |
rs186291455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896442 | ACTTTGTCTTTGAGA[C/G]CACCACTTGTCACCA | 83860 |
rs186314164 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7827626 | CTCTACTAAAGATAC[A/C]AATATTAGCTGGGCG | 83860 |
rs186324586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7867313 | AAAAGATGTGATTTT[A/T]AAGTATGCATTTTAA | 83860 |
rs186343192 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7916928 | TTCGTACTCAATTAT[G/T]TTCTTCAGAAATATA | 83860 |
rs186345380 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981919 | ATCAATATGTATAGA[C/T]ACTTGTCTTTGAGTG | 83860 |
rs186353618 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:8003513 | TAAAATTATGCATGG[A/G]TAAATTTTGTGTTCA | 83860 |
rs186356575 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:8007822 | TAACCTCTAACTTCT[C/T]ATAGGTCCTCAATAA | 83860 |
rs186360901 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975606 | AAGGGTTGGGGCAAG[A/G]TAAGTTGATAATTCA | 83860 |
rs186370686 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7981292 | CCACCCTTGCCCTCG[A/G]GCAGTGGGTCCCCCA | 83860 |
rs186378946 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7898188 | AATTCATTTTTTAAA[C/T]GTAAATAGGACTGAG | 83860 |
rs186389627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938571 | ACAAAAAAAAGAAAA[C/T]GTGAGCCTCCTTTAA | 83860 |
rs186390381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902651 | TCAGATGGTGTCTAT[C/T]GGATGTTTTTCATGT | 83860 |
rs186411868 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942975 | CGTCACAGCCCTGAC[G/T]GTCCCATTCAACCAC | 83860 |
rs186566605 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956380 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 83860 |
rs186602490 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7918067 | TATTATGGCATATTT[A/G]TATGCTCATGGATGG | 83860 |
rs186607481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986991 | CCCAGGTTAATCACT[A/G]CTGACTGTGCCGTGT | 83860 |
rs186629370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013637 | TATGCCTGTTTATTC[A/G]GTTAACAGTATAAAG | 83860 |
rs186629449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963401 | ATTTCCAGATCCTGA[G/T]GTTAGGGCCAGACCA | 83860 |
rs186632729 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7983048 | CAGGGGTGGATGTGA[C/G]TTCGGCGGGGCCACC | 83860 |
rs186651740 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7833352 | CCTTTTCTCCACATC[A/C]CTGCTAACACTTGTT | 83860 |
rs186675034 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968081 | GAAATGCGGTTCCAT[A/G]TGGTCCGAGAATTTT | 83860 |
rs186733282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866831 | AGGTTGAAAACAAAG[A/T]GAAGTGGTTTATTAA | 83860 |
rs186767509 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7825318 | GATGCCAGCAATTAC[A/T]TTTACTTATGATTTT | 83860 |
rs186894785 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7907960 | GGCAGCAGCAGGAAT[A/T]GAAAGAAGAGGCTCA | 83860 |
rs186923397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882138 | AATTATGGGAAAACA[A/G]TTATAAATTTCAAGA | 83860 |
rs186928578 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7954597 | GCACTCCATAGGTGA[A/C]TGAATGAATTAGTCC | 83860 |
rs186935673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7988328 | GGCACAGTGGCTCAC[A/G]CTTATAATCCTAACA | 83860 |
rs186936705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7972983 | GGACTCACAATGTGC[A/G]TCAGAGAGTTAAGGA | 83860 |
rs186942326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926866 | TTATCGTAACAACTT[C/T]TTGTAGCATTTTAGT | 83860 |
rs186944329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7904196 | GGGACACGCTCTTCC[A/G]AGGCAGTGGGTTATC | 83860 |
rs186953736 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993525 | AAGAAACCAGATCTT[C/T]TGTTCAGCAGAATAT | 83860 |
rs186954620 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7849142 | TTAACTCATTGAATC[C/T]TCATAATAATCCTGT | 83860 |
rs186957775 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7944384 | AGTCCTAATTTTCTA[C/G]TTAGTCAGTAAGACC | 83860 |
rs186964410 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7870029 | CAGGTGAGCATCTTT[A/T]AAAAAATTAGATAAT | 83860 |
rs186970378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948107 | TCACTCTGTTGCCCC[A/G]GCTGGAACGCAGTGG | 83860 |
rs186971827 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7852877 | TGATCCCTTTTCTTC[A/G]TTCATCAGTTTTCAA | 83860 |
rs186978705 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7887509 | CTTTTTCTTTCCCCA[C/G]TTCTGCTGCTTTTAG | 83860 |
rs186993536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820048 | TTACCTTTTGCCAGC[C/T]TGCCATGCTAATCTG | 83860 |
rs186995266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994887 | GGCTGAGGCATGAGA[A/T]TCACTTGAACCCAGG | 83860 |
rs186997270 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855244 | AAATGGTTGAAAATC[C/T]GTTTAAGAAGCAAAT | 83860 |
rs187009492 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014870 | CCTGTGGATAAAGAA[C/T]CCAGGAGGACTGAGG | 83860 |
rs187020319 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828286 | GTAGTGTTACCATCA[A/C/T]GTGCTGAGGATCTGA | 83860 |
rs187036010 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7869462 | ATGTCTGTTAACTTA[C/T]CCTCATGGGAGCATA | 83860 |
rs187043663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928486 | ATTGTGTCATAGTTT[G/T]TATGAATTTCCTAAC | 83860 |
rs187066161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852661 | CAGAGTACACATAAT[A/G]TCAACATAATATCAT | 83860 |
rs187067639 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816636 | TGAAGGGCCACTCCA[C/G]CTTCTGCACACTATG | 83860 |
rs187072117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837074 | TCTATAAAAAATTTA[A/G]AAATCTGGCCAGGCG | 83860 |
rs187104851 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7863564 | GCAGCGAGCTGAGAT[C/T]GCCCCACTGCACTCC | 83860 |
rs187127331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966374 | AAGTAATCCCACATG[A/G]CAGAAATGTTTGACC | 83860 |
rs187138251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8009695 | GGTGAGATCTCAGCT[C/T]ACTGCAACCTCCACC | 83860 |
rs187150988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929014 | TTTATTCTTTTGTTG[C/T]AAAGCAAAATTAGCA | 83860 |
rs187183278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7908038 | GCAGCGTATGGAATT[C/T]GCCCTGTGCCCACAG | 83860 |
rs187186672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7970747 | TTAATGTTTCTTTAT[C/T]CCCAAGTCCTGTAGG | 83860 |
rs187190683 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7929870 | GAACAGTAAGAGTAG[G/T]TCCAAGTAAGAAATT | 83860 |
rs187194292 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948550 | TCTCATAATAATCTT[C/T]AAATCCTGAATTGCT | 83860 |
rs187197207 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7874882 | TTATGTATTGAGCTC[C/G]GGTTTTTTTCCTTCT | 83860 |
rs187197908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8012353 | AAATTCCCTTAGCTC[C/T]GGTTTCCCCATTCAT | 83860 |
rs187204737 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7890852 | AGCTTTCGATTTAGG[A/T]TTCCTTAGAAATAAG | 83860 |
rs187210383 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7839090 | TCCTGCCCACTTGAC[A/G]TGTTAGTTACTTGCC | 83860 |
rs187211821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7935127 | ATTAAAAATACAAAA[A/G]TCAGCTGTGCGTGCT | 83860 |
rs187229235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999263 | AATACTGCAAGTAAT[A/C]CAAAGACAAGATACA | 83860 |
rs187244316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967725 | AGTACCGTATCTGAC[A/G]CATAAATGTCAGTAG | 83860 |
rs187252671 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988856 | GTTTTGGAAATAAGT[A/G]TCTATTATAAATCCC | 83860 |
rs187261982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7873024 | TTTAAAAACAAACAG[A/G]AATCTTATTTCAAGA | 83860 |
rs187262307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7906938 | ATTCCTAACCTAACA[A/G]CGTGATTCTTATCTA | 83860 |
rs187273267 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824253 | TTACTACTTTTTCTT[A/G]ATATTTAAAAATATA | 83860 |
rs187337279 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825971 | TCCTATCAGCAGTGC[C/T]CAAGGGTTCCAATTT | 83860 |
rs187404922 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7991219 | CATACATACACATCC[C/G]TATGCATGTATATAT | 83860 |
rs187426660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7913477 | CAGAAGCTTGATCCT[A/G]CTTTTAGAAGATTGC | 83860 |
rs187436657 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7951889 | ACATGTCTCTATGAT[A/T]GTAGGGTTTTTATTC | 83860 |
rs187511489 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7940325 | TCAATTTAATTAAAT[C/G]TAATAGATATTTAAG | 83860 |
rs187513082 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7957780 | TGCTGTCTGTCTCAC[A/G]CTCTCTCTAGCGCGC | 83860 |
rs187519395 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7978530 | TTTTCGGTTGTGCCA[A/G]TAGAGACCTAGGAAA | 83860 |
rs187533653 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7918952 | ACAGCTTGCTGCGTG[G/T]TATACAGAAGAAGAA | 83860 |
rs187547281 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7830725 | CTGACCTCAAGTGAT[C/G]CGCCAGCCTCGGCCT | 83860 |
rs187563147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839827 | TTTTAGAAATCTCTG[C/T]GTCTCTTGCTTTACA | 83860 |
rs187599052 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7898722 | TAGACTCTCTTTAAG[C/G]TCTTCAGACAATTAA | 83860 |
rs187603394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883343 | CTGATATTCCTCATC[A/G]AATTCAGGGTGATTA | 83860 |
rs187605104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873814 | GAACTTAATGCTGTT[C/T]ATAGATAGAAAACTG | 83860 |
rs187619854 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7890582 | TACAGTCAAGACTCT[G/T]TCTGTGAGTGTTGAT | 83860 |
rs187621571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839485 | TAATGGAGGAGCAGT[C/T]GCAAAAATTAGCTTG | 83860 |
rs187622708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918699 | GAAGCTTAGCTAGGT[G/T]TTGGATGTATTATAT | 83860 |
rs187624164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7821116 | CAGGGGTCACTGCAG[C/T]TCTTCAGTGTAAACC | 83860 |
rs187630688 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855769 | AGAGGAAACAGTCAT[G/T]CAAGAGGAATTAATT | 83860 |
rs187635824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7820537 | TCTCACTCTGTCGCC[A/G]AGCGTGGAGTGCAGT | 83860 |
rs187643921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865155 | AGCTTCAGGAGTGGA[A/G]AGGGCAGGGAATAGT | 83860 |
rs187645480 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7846217 | CCGCCTTGGCCTCCC[A/G]AAGTGCTGGCATTAC | 83860 |
rs187690004 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7843019 | TTTGCACCTGCTAGG[G/T]CGTAGTCTGTGTCTG | 83860 |
rs187694917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878980 | CAATCCGCTCACCTC[A/G]GCTTCCCAAAATGCT | 83860 |
rs187696398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7939424 | TCTTACAATGTAGCC[C/T]GCCAGTTAGCAAAGT | 83860 |
rs187724216 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953178 | ACGTTGTTTCACTTC[A/G]GTTCCATTTTCCCAG | 83860 |
rs187724863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004611 | TGTTATTCCACTATC[C/T]TCTAGATTTCATCAT | 83860 |
rs187759101 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7894912 | GGTTTTTGAGACTCT[G/T]CCACCCAGGCTGGAG | 83860 |
rs187763038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925557 | GCCTGTAATCCCAGC[A/G]CTTCGGGAGGCCAGG | 83860 |
rs187764831 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7943904 | ATGAGCAATTTCTAA[A/C]AAATCATTACCCCTA | 83860 |
rs187765986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914577 | TGCATCTCAAAAGAG[C/T]GTATGAGAAGAAATT | 83860 |
rs187779171 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7915615 | GCCACTGCACTCCAG[A/C]CTGGGCGACAGAGCG | 83860 |
rs187786321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824871 | ATATTAGGTAAATTA[C/G]AAAACATTTGAAACA | 83860 |
rs187796005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7879400 | ATATTTTATCTCATA[A/G]GGTTTTGAGTCAGAA | 83860 |
rs187800743 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844178 | CTAAAACAGAATTTC[C/T]TTTAATAAAGGCTTT | 83860 |
rs187803804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968304 | GCAACTCTCCCAGAC[A/G]CTGACCCAGATCGGC | 83860 |
rs187804774 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7861259 | TGAGCCACCGCATCC[A/G]GCCCTGCACGGCTAA | 83860 |
rs187817438 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7989269 | GAGGTAGGATAAAGC[C/T]CACTCAGGCCACATG | 83860 |
rs187841849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820720 | GGCTTGTGTCAAACT[C/G]CTGGGCTCAAGTGAT | 83860 |
rs187856030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887336 | AAGGGGTTGTTGTGT[A/G]CAATCGTTGACCTGT | 83860 |
rs187872763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010383 | TGTAAATGTAGAGAC[A/G]CATGGTGGTACTGAA | 83860 |
rs187897430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004311 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACGGG | 83860 |
rs187917859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926790 | AGTTCTCTTTCAAGT[G/T]TAAGATTAGTAAGCA | 83860 |
rs187926459 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7962901 | TACATTATATGCTTA[A/G]TTAAAATGTGTTGGG | 83860 |
rs187959742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7927955 | TCAAAATCTGGACAT[C/T]GTTTTTTTGCTCCCC | 83860 |
rs187963737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946898 | AATACTTACCCTACT[C/T]GTTAAAACTTTTCTT | 83860 |
rs187967824 | snp | C/T | 3.34068e-05 | 0.00408684 | missense | TAF3 | GRCh38.p7 | 10:7964967 | CACCTTCAAATATGC[C/T]CCCCAACTTTCCTTA | 83860 |
rs187971492 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015697 | AGCCTGCGCAGTGCC[C/T]GGAAACATGGTGGGG | 83860 |
rs187971866 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837318 | CAGTGAGCCGAGATT[G/T]CACCACTGTGCTCCA | 83860 |
rs187996016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7900801 | TTGCTCTTTAGGCTT[C/T]GTATTAAGAAGGTAA | 83860 |
rs188031115 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7987365 | TACACATACTGTTCA[A/G]CAGCTTATCCCCTCC | 83860 |
rs188032062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7971902 | TCAGGTGAAAGAAGT[A/T]TTGCTTCTACATAAA | 83860 |
rs188034915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979099 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 83860 |
rs188037428 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008409 | CAGCCTGAACGGTCA[A/G]TCTTTAAAACCTGGC | 83860 |
rs188046220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894538 | TGGTTGAACTGTTAA[A/G]AGTAGAACAATGATT | 83860 |
rs188062423 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7940918 | GAGCTATGATCACAC[C/T]ACTGCACTCCAGCCT | 83860 |
rs188063747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935869 | AATGGCCTAGTACAG[A/G]GGGTGTTTATAGACC | 83860 |
rs188072346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842665 | GTATGTCATTGAAGC[A/G]TGACAGTTCAAAGCC | 83860 |
rs188077732 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:8010175 | GCCTCCCAACGTGCT[A/G]AGATGACAGGCATGA | 83860 |
rs188132359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904015 | GAAGTTTCACGGTGC[A/G]TCTGAGTTGGAGCAG | 83860 |
rs188173848 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7982670 | TTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 83860 |
rs188204102 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943973 | TTATACTTTGAAAAG[A/G]GGGTGGGTTTTCTTG | 83860 |
rs188264439 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884369 | GCCCTGGAAGCAGCC[A/G]TTTCTCCAAAGAGCT | 83860 |
rs188297256 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7856294 | CAGCCTGGCCAGCAT[G/T]GTGAAACCCCGTCTC | 83860 |
rs188325189 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8000254 | CCTGAGTAGCTAGGA[C/T]TACAGGCATGCACCA | 83860 |
rs188342167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869038 | AATTAATTCAGAGTG[C/T]AAAACAATACATCGT | 83860 |
rs188346938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920449 | GTTGAGCTTTTTATG[C/T]TTTGCATTTTGTTCT | 83860 |
rs188348486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7836313 | TTTTTTTTTTGAGAC[A/G]GAGTTTCGCTCTTGT | 83860 |
rs188361819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7959094 | GCAGTGAGCTGAGAC[C/T]GTGCCATTGCACCCT | 83860 |
rs188403870 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819449 | AGGCTGACTTTGTCA[A/G]TTTCGCTGATTAGAT | 83860 |
rs188448492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936367 | GTTGGGGAGATAAGA[C/T]GGGGATTTCTCTTAC | 83860 |
rs188454468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888379 | CTTCTATTTATTTTT[A/T]TCTAAATTTATAAAA | 83860 |
rs188457632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7845051 | GGTTTTTGACACATA[C/T]TACCCATTGATTTCC | 83860 |
rs188469470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8010781 | TGGGCATGGTGGCAC[A/G]TGCCTGTAATCCCAG | 83860 |
rs188473854 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7854387 | ATTTCTAGGTCCACA[C/T]TGTTATGCGAGCCGC | 83860 |
rs188475793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895193 | GGCAATTTCCTTGGT[A/G]ACTTGATAACAGCTT | 83860 |
rs188476366 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7827282 | ATCTGTAAAATAAGT[G/T]TAATAACACCTACCA | 83860 |
rs188477053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846562 | GTTTTGAGTGGTTTT[A/G]ACTAGTTGAAAAGAT | 83860 |
rs188484190 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7838012 | ACATAATATATTCAT[A/C]AACATTATCTCATTT | 83860 |
rs188486057 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7916114 | CACCTCTTAACCCAA[A/T]GTGTTTGGTTTGGAT | 83860 |
rs188488342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871890 | ATCCAAATATTTCTA[A/C]TATTTGTTCATCACT | 83860 |
rs188559759 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883716 | ATTTTCCCCTCCTTC[C/T]CACTTATTTATTCAT | 83860 |
rs188601438 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7950708 | AGCAAAAATTCAGTC[A/G]CATGCGTTGCCTGTT | 83860 |
rs188617809 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7969923 | CTCCTTCCTCCCATT[C/G]AAAACTAGGAAGAGA | 83860 |
rs188625848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7892644 | TCAGTTCTGCTGTAA[A/T]GTTTGGGTTGGTTTT | 83860 |
rs188630792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857434 | GAGCTGGAGGAGAAG[A/T]TGGCAGGACGCCTAC | 83860 |
rs188631339 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7851925 | GCTGAGACTACAGGC[A/G]TGAGCCACCATGCCT | 83860 |
rs188641925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7911076 | TTTTGACTTTAATTA[A/T]ATGATTTTTGAGGGA | 83860 |
rs188673180 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7990358 | AGTGAGCAAGGCAGA[A/G]TGGCTGGCTACCTTT | 83860 |
rs188679420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997706 | GGGACCAGCTGTGGG[C/T]GGTATTGGTTTCTCT | 83860 |
rs188680471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011339 | ACTCACTGCAGCCTC[A/G]ACCTCCTGGGCCCCA | 83860 |
rs188687024 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7865626 | TGGCTTTAGCAGCCC[C/T]GGCAGGGTGGATGCA | 83860 |
rs188709766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957310 | GGAGATTAGGGCAGA[C/T]GGCTGAGGTGAATTC | 83860 |
rs188709926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7891489 | AGCAATAAATGTATT[A/G]AAAGGCATGGTTAAG | 83860 |
rs188714019 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7930763 | TCTATAGATATACTC[A/G]ATACTGGTATCCATT | 83860 |
rs188725068 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7832589 | CGCACTGTCACCCAG[C/G]CTGGAGTGCAGTGGT | 83860 |
rs188773961 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7865392 | GCTGAGGCAGGAGAA[C/T]GGTGTGAACCCGGGA | 83860 |
rs188777964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7831198 | TTATATAGGGAAAGC[A/G]GGGTTAACGCTTGAT | 83860 |
rs188825807 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903504 | TTTAATAAGGACAAC[A/G]GTGTTTAACTGTATT | 83860 |
rs188835944 | snp | A/G/T | 0.00028588 | 0.0119527 | intron-variant | TAF3 | GRCh38.p7 | 10:8014631 | TGAGCTTGTTTTCAC[A/G/T]TGCAGGCCCTGTGTT | 83860 |
rs188851750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900307 | TTGTAGCAATTATTG[A/G]TAAATTATACTTTTA | 83860 |
rs188858049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936132 | ATAACACGTGAACCC[A/C]GGGGACAACAAGGAA | 83860 |
rs188866862 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7972452 | GATATATCCTGGTTT[G/T]CCTGGGACAATCCCA | 83860 |
rs188875398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961138 | GAAGAGGTGCTGAAT[A/G]TTGATATTAACAAGA | 83860 |
rs188887421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981271 | CTCCCTCTTCCATCT[A/G]TTCACCCACCCTTGC | 83860 |
rs188895460 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8001517 | TTATTGTTGCAAGTA[G/T]TTTGCTTCACTTTGT | 83860 |
rs188925011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7875719 | GTTTAGTGAATTTAC[C/T]CCCCAAAGCCTCTGG | 83860 |
rs188943812 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7840403 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 83860 |
rs188961718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949462 | AGCCAAGCAGGCCCC[C/T]ACCTGTCCTAGCCTT | 83860 |
rs188981641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909145 | CTAGACCAAGTGTGG[A/G]CCTCTGACCTGCAGT | 83860 |
rs188983321 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7995310 | AATTTTTCTAAAACT[G/T]AACTTTCTGAATATG | 83860 |
rs189000171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7977093 | TCAGTTGTACAGAAT[A/G]GCCCAGATTGTCTTT | 83860 |
rs189006078 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7916632 | TGAGCTTTTAAAAAT[A/T]AAGTGTATATATATA | 83860 |
rs189013052 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | TAF3 | GRCh38.p7 | 10:7954740 | ATAGGTGAATGAGTG[A/G]ATTAGTCCTAGTTAA | 83860 |
rs189043985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7821398 | CTGAGCATCACTTAC[A/G]AACCAACCCCTGTAC | 83860 |
rs189086367 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7887180 | GAGCTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 83860 |
rs189093328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891696 | CTGTTTATCACTGCC[C/T]GGCTAGACTGAATGT | 83860 |
rs189103200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910336 | CATACAAACATCTAA[A/G]TATCAGGACTTTTGA | 83860 |
rs189106665 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994526 | ATTTATTGTTATTTA[A/T]AAAATAGAGATGAGG | 83860 |
rs189125202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840794 | ATTGCCTTTTATTTA[A/G]CTAATGACTGCTTAC | 83860 |
rs189125258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7876155 | AAATTAATTTTGTGC[A/G]GTGTTTTATATTTTT | 83860 |
rs189131570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858416 | CCTGGATGATACAAT[C/T]GTTTATGTCAGCTAG | 83860 |
rs189142641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7953925 | CATAGGTGAATGAGC[A/G]GATTAGTCCTAGTTA | 83860 |
rs189258735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973496 | GACTGCATTCCGTCT[C/T]AGTTTTGCTATTTGT | 83860 |
rs189281323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991154 | TTGGAAACTTTCTTA[G/T]GTACATAGATACATA | 83860 |
rs189291920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937232 | ATCCTATGGTAAGAG[A/T]ATGTTTAGTTTTGTA | 83860 |
rs189292251 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817534 | GCATATTTAAGAAAC[C/T]GCATAGTTCAGCCAC | 83860 |
rs189293205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011734 | ACTTAACCTCCTTGA[C/T]CTTCGTGTCTTCATC | 83860 |
rs189328053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881444 | AAAAGGACAATAGTT[A/T]AATCAAGTAAAAGAC | 83860 |
rs189329282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7848645 | AGGATTTCTTAAAGT[C/T]CAGCCTCAAATGAAG | 83860 |
rs189370645 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921976 | TATTGAAATATAAAT[A/G]TATAATTTTCCATCT | 83860 |
rs189383028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7941632 | CATCCTTGCTGCGCC[A/G]ATGCCTTCGAGGCTG | 83860 |
rs189398545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866505 | ACAGAGAAGAGTGAG[C/T]GCAAAACCTCTGAAG | 83860 |
rs189410236 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7901289 | TTTCCAAACCTCTGC[A/G]TAGTCCATGCCACAG | 83860 |
rs189410706 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884596 | TTTCATCGTGTTGGC[C/T]GGGCTGGTCTCAAAC | 83860 |
rs189434570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7826552 | AGCAAAAAAAGAAAC[C/T]CATTTAGTTTTATGC | 83860 |
rs189440436 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7862001 | AGTCTTTATTCTGTC[C/T]GTTCTTCCAATTTGA | 83860 |
rs189446429 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7960127 | TTTTGGCATCATTGG[G/T]ATTTATGAACCTCTG | 83860 |
rs189474524 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7845322 | TGTGTGTGTGCGTGT[G/T]TGTGTGCACACGGTT | 83860 |
rs189485381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927172 | TATACTCATCTTTCA[C/T]GTCCATGAGTTTAAA | 83860 |
rs189488820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7827728 | GAGCTTGCAGTGAGC[C/G]GAGATTGTGCCACTG | 83860 |
rs189526402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917387 | TAGATGCTGTCACAC[A/G]GAAACCAGCTGTGCA | 83860 |
rs189526459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963748 | AATTAACAGGGCACA[C/T]GTATACCTGTGTAAC | 83860 |
rs189526848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8007178 | AAAACCTTTGGCTTA[C/T]TAATACCATGGAATA | 83860 |
rs189531928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7937858 | TTTTGTAGAAGTGTC[A/G]GCAAAGGAACAGTGA | 83860 |
rs189532280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7984857 | GGATGCTATCTGATT[A/G]TAATTTCTCCTAAAG | 83860 |
rs189533928 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955699 | AGTCAATATTTATAG[A/T]AGCTTAGAATTAACC | 83860 |
rs189546798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7888918 | TATGCACACTTCCTC[C/T]GGTGTATATTGTGTC | 83860 |
rs189547827 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7863052 | TGGAATGGCTGTGAA[C/T]AATAAGCTATGCTTT | 83860 |
rs189556165 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7897142 | AAGGTTCACGTGAAG[A/T]GATCAGGCCCGCTTG | 83860 |
rs189562095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881636 | ATTTCTAGGGGGCCC[C/T]TTGAAATTTGATAGA | 83860 |
rs189562515 | snp | G/T | 0.029116 | 0.117091 | intron-variant | TAF3 | GRCh38.p7 | 10:7846064 | CCTGGGTTCACGCCA[G/T]TCTCCTGCCTCAGCC | 83860 |
rs189563213 | snp | C/G | 0.000233922 | 0.0108123 | missense | TAF3 | GRCh38.p7 | 10:7964584 | TAAAGAGACTATCCA[C/G]GTAAAACAAATACAG | 83860 |
rs189563973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864947 | TTTTAGGTTTTGGGT[A/G]GCTGGGGTGGGTGGC | 83860 |
rs189566019 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7906209 | CTGAAGTTATAGTTT[C/T]AGTGTCTTATCTTTA | 83860 |
rs189588886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005650 | TTCTGCTTACCTCTC[A/T]GGGTTCCTGCTTTTC | 83860 |
rs189594260 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7841052 | GAGGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 83860 |
rs189629405 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7896252 | TATTCTTTTTCTCAG[A/T]TCTTTACTCTTGTGA | 83860 |
rs189644535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862552 | TCAGTAAACTGTACA[C/T]GTTTATAACATTTTT | 83860 |
rs189667128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876421 | AAATGGGCCATAAGC[A/G]GGTATTTTAAAGTAC | 83860 |
rs189719367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7844490 | CAAGCGATTCCCCTG[C/T]CTCAGCCTCCTGAGT | 83860 |
rs189738977 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981294 | ACCCTTGCCCTCGGG[C/T]AGTGGGTCCCCCATG | 83860 |
rs189750708 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7905166 | AGAATACAACTCAAG[C/G]GGGGCTATTTATGAA | 83860 |
rs189777538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879949 | CACGATGGGTCACAA[C/G]AGTAATCCTGGCAAC | 83860 |
rs189823687 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7946198 | CAAATAAAATTCACA[C/G]TCTTTCCCATGATCC | 83860 |
rs189827101 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7949995 | CACATTTTAATAAAT[G/T]AGAGTCAATGATACA | 83860 |
rs189835098 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923645 | GCTTTGGTTTTCATC[C/T]TGTATTCAATAGAGT | 83860 |
rs189839091 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7989728 | TGAATCATAAGCTTC[A/G]GCATTTCTTTAACAA | 83860 |
rs189839752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7985983 | GAGACAGGGTTTCGC[C/T]TTGTTGGCCAGGCTG | 83860 |
rs189854376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014012 | ACTGCAAAACCCAAG[A/G]GTGCTTAGACTATTG | 83860 |
rs189859406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822145 | AAAATTGTACTGACA[G/T]TGATGTGCATAAGAG | 83860 |
rs189864294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858734 | ATTCACATGCTTAGC[A/C]CATGTTAGCAGCTAT | 83860 |
rs189870401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830130 | TGGACTCAAGAATCT[A/G]TGTCCACTTCAGTAC | 83860 |
rs189877817 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7872094 | GAAAGTCAGCGAAAT[G/T]TCCATAATTAAAGTT | 83860 |
rs189947535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002130 | CACAACTCTCTTCTT[C/T]CTATCATCCTCTGTT | 83860 |
rs190079973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7902371 | GAGGTTTCTGTGAGC[C/T]GAGATTGCACCACTG | 83860 |
rs190086466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969061 | ATGCTCCCAATAGTT[C/T]AGGAGGCCAAGGCAG | 83860 |
rs190117653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834514 | CTCGGTTGTTCATTG[G/T]TTCTAGGCAATAAGT | 83860 |
rs190148149 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7849408 | TATTTGGGATATGTT[A/G]TGCCACTGGTGTCAT | 83860 |
rs190151249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839650 | GTATTGTGGCTCTTC[A/G]TTTGTTTCTTTTCCT | 83860 |
rs190154715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885100 | ATGGGGAGTAATTGC[G/T]TAGTGGCTACAGAGT | 83860 |
rs190160067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856144 | TTTTTAAAATGCAGT[C/T]GAGAACTAGAAAATA | 83860 |
rs190163139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885707 | CTTCATTATCTCCCA[A/G]ATAATCAACCTTTCT | 83860 |
rs190168281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820695 | AGATGTGGTCTGGTT[A/G]TATTGCTCAGGCTTG | 83860 |
rs190183438 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7849924 | GAGCTCGGGCAGTCT[A/C]CTCACCTTGGCCTCC | 83860 |
rs190199118 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929094 | GAGGTTTTTGCCTTC[C/G]AGACTGTTCTCTATC | 83860 |
rs190200307 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7867395 | CTAGAATTTTAATGC[C/T]GATGCTGAGATTTTA | 83860 |
rs190201074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956217 | AAAATAGGCCGGGCG[C/T]GGTGTCTCACGCCTG | 83860 |
rs190203012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907993 | TCAGGAGATACGTAG[A/G]AGAAGTTGGCAGTGG | 83860 |
rs190205292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974846 | TTTGGGAGGTCGAGG[C/T]GGGCGGATCACGAGG | 83860 |
rs190217393 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996221 | CTGGGACCATAGGCA[C/T]CCAGAGGCTTCTGTG | 83860 |
rs190225773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7873953 | CGCTGTGTTTCCCCT[C/T]GAGAGGCCATTGCAG | 83860 |
rs190240128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833325 | TCCCACCAACAGTGT[A/T]CAAGGATTCCCCCTT | 83860 |
rs190243316 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7890752 | TTTTAACTTCTAATT[A/C]TTTTGGTTTATTTTT | 83860 |
rs190245212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938059 | ATACCTGTATTTAGA[C/T]GTGAAGTATGAATGT | 83860 |
rs190305832 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7892875 | CAGGCTGGAGTGCAA[G/T]GGCGTGTGATCTTGG | 83860 |
rs190348575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952756 | TTGGTTGTAATGTAT[A/G]AATTGTCATTGCCTA | 83860 |
rs190350675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7971752 | GCCGCACTGCTGGTG[C/T]CCTGGAAAAATGGAG | 83860 |
rs190357822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982446 | CTCTGTTGCCCAGGC[C/T]GGAGTGCAGTGGTGT | 83860 |
rs190360929 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7993110 | ACCAGGATCCAAACC[A/G]GACTTATATCTCATA | 83860 |
rs190362215 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003871 | GGCAACAGAGCAAGA[C/T]GCCATTATCAAAGAA | 83860 |
rs190371863 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7914376 | TGTTTTCCCCCTCCT[A/G]TTTCAATCATTTCAC | 83860 |
rs190377401 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8001023 | GTTTGTTCATCATCT[A/G]TGTAACCGATCTCCT | 83860 |
rs190381895 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7970383 | GAGGGTTTGGTATAG[C/T]GGTTCCTGTTTTACA | 83860 |
rs190383270 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935437 | AAAAATACAAAAAAT[A/C]GCCTGGCGTGGTGGC | 83860 |
rs190389417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7867143 | ATGCCCCTGTCATCC[C/T]AGCTACTCAGGAGGC | 83860 |
rs190397231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7962787 | CTGATCACTTTCTGT[C/G]GGCTAGACATATCTG | 83860 |
rs190409752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931934 | GATGAAATAATAGAA[A/G]TGTACTGGGTCTTGA | 83860 |
rs190411877 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7871139 | TAGTTCACTTAAAAG[C/T]TTCCTATCATACAAT | 83860 |
rs190418624 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7833383 | ACCTTTCATCTTTTT[A/T]ATAGCAGCCATTCTA | 83860 |
rs190419574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7837472 | GCATGGCGAAACCTC[A/G]TCTCTACTAAAAATA | 83860 |
rs190421144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012769 | AGTGAAACATATATG[C/G]ACCCCCAATGCACCT | 83860 |
rs190448926 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7935146 | GCTGTGCGTGCTGGT[A/G]CGCGCCTGTAATCCC | 83860 |
rs190453125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913747 | GACAGCAGATACTTG[C/T]GCCTCTTTAGGGATA | 83860 |
rs190465128 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7904479 | TACACCTAGTAGTCT[A/G]TTAGTGCCTGATACA | 83860 |
rs190466993 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7877914 | TTTCTATACTGTAAC[A/G]GCAATTCAGATCTCA | 83860 |
rs190475792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859892 | TCATAATGATTATTA[C/T]GCATCCTTGGTTCAT | 83860 |
rs190479494 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7945351 | CTTATTTACTTATTA[A/C]TGTGGCATTTTTTCC | 83860 |
rs190480034 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7893358 | GTGCCTTTGGATTTG[A/G]TAAGTTTATCACTTA | 83860 |
rs190518915 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974315 | CAGCCAAGAGTGATG[C/T]TGGCTAGGGGGAAGG | 83860 |
rs190535581 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016060 | ATTTATTATATGTTA[C/T]AGATGTCTGAGAGGT | 83860 |
rs190544848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877480 | TTCTTTAAGACACAT[A/G]GAAAAAATTGTCATA | 83860 |
rs190555523 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7912349 | AAGCGATCATTCTGC[A/G]TTGGCCCCGCAAAGC | 83860 |
rs190605229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918509 | GTTCAGTCTGTGGCA[C/T]AGCTAGGAACAAGAG | 83860 |
rs190623600 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7882947 | TTTTTTGTTTCTGAA[C/T]TGTTTGAAACTAAGT | 83860 |
rs190624490 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7980136 | AATACTCTTTTGAAG[C/T]GAAATTAATGAGCAG | 83860 |
rs190626409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951572 | CATTTGCCCATTGGC[C/T]AAAGCAAGTCACACA | 83860 |
rs190635249 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7996691 | GAGGCAGGGTCTCAC[C/T]CTGGGATTTTTTTTG | 83860 |
rs190644912 | snp | C/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853668 | ACTGCCTGGCCTGCA[C/G/T]CCTGATTCTGTAAAT | 83860 |
rs190654614 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7888008 | CCTGCCACCACCGCC[A/G]TTGTGGTGAATGTCA | 83860 |
rs190664803 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818224 | AACTCTCTAATATGA[C/T]TAACGTTATTAGTGC | 83860 |
rs190670195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956883 | TTTTAGTTAAGATTT[G/T]TTTGAAAATAGGTAT | 83860 |
rs190732358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926974 | GGGGTTGAGAATCCA[A/G]AGATGAAAGTGGCCT | 83860 |
rs190777743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995918 | GATTCTCATAATTGT[C/T]TTTGGGTATTTGGTG | 83860 |
rs190791034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7842074 | CAGAGGCCCTCCTAT[C/T]GTTCATTGAGTTGCG | 83860 |
rs190810940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868134 | TCCACATATAAGGGG[A/G]CATGTGTAGTTCAAA | 83860 |
rs190812118 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8003050 | CCCTTCTATTGCTAG[A/C]TGTTCCTCTGGGCAT | 83860 |
rs190818477 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7972100 | CCTTAAAAGCTCATC[A/G]TGGCCCCAGATTTTG | 83860 |
rs190838567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898232 | CAAAATTGACACAGG[G/T]ACTCAACAGTGTCAT | 83860 |
rs190854187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943489 | TAAAACCATGGCTTC[C/T]AAACCTCACACCATG | 83860 |
rs190855209 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938654 | AATAGTCAAGCCAAG[A/G]TGCCTAGTAGGAAAT | 83860 |
rs190866185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981704 | TGATTTCTTACAATT[A/C]AGTAACTTCATCATC | 83860 |
rs190875787 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7887053 | ATCCTGGCTAACATG[A/G]TGAAACCTCGTCTCT | 83860 |
rs190884007 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7925381 | TTGTAGGCAACAAGT[A/T]AATGCATGTGAATAT | 83860 |
rs190888782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903211 | GGGCAACAGAGCAAG[A/T]CTCTATCTCACAAAA | 83860 |
rs190927335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976507 | GTAAGCTCCGCCTCC[C/T]GGGTTCACACCATTT | 83860 |
rs190949451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854618 | CTTGAAGGATAAGAT[G/T]TAAATTTCAGTGAAG | 83860 |
rs190957362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841558 | GGTTAGGATGATTTC[A/T]TTATAAATTCTGTTG | 83860 |
rs190967032 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819817 | TTTGTTAAAGTGGTT[A/C]CTATACTGGAAAATT | 83860 |
rs190976267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823550 | CTGAGAGGGGAAGAT[C/T]GCTTGAGCCTAGAAG | 83860 |
rs190991284 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | TAF3 | GRCh38.p7 | 10:7939593 | ACACACACACACACA[C/T]ACACACACACACACA | 83860 |
rs190992952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7988309 | AAAAAGATATCCGGG[A/G]CTGGGCACAGTGGCT | 83860 |
rs191001876 | snp | A/C | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009147 | CAGGCCGAAGACCCC[A/C]CCGCCGGCCCCCGCG | 83860 |
rs191003620 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957673 | TATGTACAGAAGAGT[C/T]CTTTTCTCCCGTTTC | 83860 |
rs191005736 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7978033 | AAACATTGATTTTTT[G/T]TTTTGGAACTCATGT | 83860 |
rs191014214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899658 | CACAAAGGAAGAAAT[A/C]AGAGGAAAAGCTTAG | 83860 |
rs191024347 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7918702 | GCTTAGCTAGGTTTT[G/T]GATGTATTATATTCC | 83860 |
rs191078382 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7993932 | TCAGTGAAAAGAGTT[A/G]ATGGAGTTGATATAG | 83860 |
rs191110162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828362 | GCTGTGTGATTATCC[A/G]CAGTGTGAAGATGAC | 83860 |
rs191164028 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897680 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTGAGAC | 83860 |
rs191195964 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838223 | AGTCGGATCCTACAC[A/G]AGGAACTGGTGTTGA | 83860 |
rs191234930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7902749 | GTTCTGATCCTCCGC[A/G]TTCATTTAGCATTTA | 83860 |
rs191246428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890974 | CAGCGTAACTGAATT[C/T]TGCTAAGCATGTAGC | 83860 |
rs191250815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7832844 | CATGAGCCACTGCAC[C/G]TGGCCCAGCATTTAT | 83860 |
rs191254265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7878308 | AAATATTATATAGCA[A/G]TGAATAAAAGGCTCT | 83860 |
rs191270445 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TAF3 | GRCh38.p7 | 10:7842810 | TTAGATATAAATGTC[A/G]TATATTTTTACAGAT | 83860 |
rs191286883 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967944 | GGTTAGGACAACCCA[C/G]GGAAATGCCATTGAT | 83860 |
rs191294903 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7989008 | TTTTATAGATTCTTT[C/T]CTGGTGTTTTATAAA | 83860 |
rs191302429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010220 | CCAAGATGCATTTCT[C/T]CATTGCAGTTTTTCA | 83860 |
rs191306293 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7884504 | CGATTCTCCTGTCTC[A/G]GCCTCCCGAGTAGCT | 83860 |
rs191312676 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866250 | GGCACGGGGGATGGA[C/G]CAGTCAATAAATAGG | 83860 |
rs191313276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943041 | GTCCAGTTTCTTTCT[A/G]TGTCTGTGTTTGTTT | 83860 |
rs191315041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908044 | TATGGAATTCGCCCT[G/T]TGCCCACAGCTCTGG | 83860 |
rs191317143 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7900826 | AGGTAAAGATTTTGA[C/T]TAGAAGCACATGGAT | 83860 |
rs191324942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7930016 | AGACCAGCCTGGGCA[C/T]GATAGGGAGGCCCTG | 83860 |
rs191325187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7949127 | GAAGTAAGTGGGCTC[A/G]GCATTATTGTGTGAG | 83860 |
rs191336587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845553 | GAGAATGTGTTTGAG[A/G]TAGGTGGTAATGTGA | 83860 |
rs191344819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882238 | GACCGTCAAGCATCA[A/G]TCTTAGCATGTTAGA | 83860 |
rs191382127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887181 | AGCTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 83860 |
rs191386482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948112 | CTGTTGCCCCGGCTG[G/T]AACGCAGTGGTACGA | 83860 |
rs191400772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917724 | ACAAGCAGTTGTGCT[A/T]CTGGACTAGATACGG | 83860 |
rs191405849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952604 | TAGGTGTCATTTCAG[A/G]TTGGCTTGCTTATAT | 83860 |
rs191425785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852210 | TTGCCTCAGCATTCA[A/G]AAGTGCTGGGATTAC | 83860 |
rs191428957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963402 | TTTCCAGATCCTGAG[C/G]TTAGGGCCAGACCAT | 83860 |
rs191443330 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7983671 | TAGGTATTTTGCCTA[C/T]GTTAAAAGCTAAACA | 83860 |
rs191451431 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:8005128 | CTCTGTGACTTCCTA[C/T]GACCTATATTTCTAG | 83860 |
rs191459068 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7926893 | TAGTATTAACAATGT[C/T]AGAGAGAAGAGTATT | 83860 |
rs191463362 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7904322 | CAAGCAAGACTGGTT[A/C]CTTTCTATTTATGCT | 83860 |
rs191466514 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925672 | TAGGCATGATGGTGT[G/T]CCTGTATTCCCAGCT | 83860 |
rs191471049 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991445 | TTTACAGTTACTATT[A/G]CACCATTGTTTTTTT | 83860 |
rs191475185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944487 | TAAAAGTTACTACGC[A/C]TTTTTTTCATGTAAC | 83860 |
rs191475738 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7860558 | ACTTGGTTGTCCAGA[A/G]GTGTAGTTCATATAG | 83860 |
rs191486121 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7894023 | CCAGCTGTAGTCTTC[C/T]ACCCTGTATCATCAA | 83860 |
rs191494258 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7924656 | ATATCCTTTAAAAAT[A/C]TATTCTTTTTTATTT | 83860 |
rs191494555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7824877 | GGTAAATTAGAAAAC[A/G]TTTGAAACAAAAAGA | 83860 |
rs191554458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7961389 | GTTCTCCATCTGTGC[A/G]TCCTTCATGCTTTTG | 83860 |
rs191610896 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7967124 | GAGTGACTTGTCCAA[G/T]ATCAGGATGACACAG | 83860 |
rs191626821 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:8009913 | GCATGAGCCACCGTG[C/G]CCGGCTTTTTTTTTT | 83860 |
rs191637585 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7869052 | GTAAAACAATACATC[A/G]TAGAACAATTCCCTA | 83860 |
rs191643421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876201 | AAATAGTGATGAAAT[C/T]GACTATTTTAGTAAG | 83860 |
rs191643879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903805 | ATTATTTTGCTTGGA[A/C]GTTCTGTGGATATTG | 83860 |
rs191669112 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | TAF3 | GRCh38.p7 | 10:7842168 | TTTTTTTTTTTGTTT[G/T]TTTTTTTGTTTTTTT | 83860 |
rs191711893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970798 | TTATTAAATTTAAAC[A/G]GTTTGTTCTTTAGAG | 83860 |
rs191716268 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7943938 | AACCAAGATGAGTCA[C/G]CTCATTATAATAGGG | 83860 |
rs191733806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8012371 | TTTCCCCATTCATAA[A/G]CTACCCAGAGGTTGT | 83860 |
rs191825622 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TAF3 | GRCh38.p7 | 10:7837088 | AAAAATCTGGCCAGG[C/T]GTGGTGGCTCACACC | 83860 |
rs191837303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852799 | TATAAAGAGAAACTT[C/G]CTATCATCTACTATT | 83860 |
rs191838684 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816945 | GTGCATATATAAATA[C/T]AAAATATATAGTAAA | 83860 |
rs191846794 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7994965 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAGAAA | 83860 |
rs191853207 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014953 | GGCTCCGTGGCAGTG[C/T]GACAGAAGGAAACTC | 83860 |
rs191869455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936368 | TTGGGGAGATAAGAC[A/G]GGGATTTCTCTTACA | 83860 |
rs191872970 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7954681 | TGAGTGGATTAGTCC[C/T]AGTTAACACAGAGCT | 83860 |
rs191876287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973030 | GGGATGAATTTGGTG[A/T]CAGGAGACCTGGATT | 83860 |
rs191888826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7869575 | TTTAACAGTGCTTTT[A/G]TTAACATTCTTAATC | 83860 |
rs191893413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904018 | GTTTCACGGTGCGTC[C/T]GAGTTGGAGCAGAGT | 83860 |
rs191896119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835055 | GAGGGATGTTTTGCT[A/G]TTTAGTCTTCTCTTC | 83860 |
rs191900463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7887345 | TTGTGTACAATCGTT[A/G]ACCTGTGAACCCAGC | 83860 |
rs191901105 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7844372 | GCTTTTCTTCTTCTT[C/G]TTGTTCTTTTTTTTT | 83860 |
rs191901265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861372 | TGTCCTCCCAAAGTG[C/T]TGGGATTACAAGCAT | 83860 |
rs191915943 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7859122 | AAAAAATTAGCTGGG[C/T]GTGTGGTGGGCACCT | 83860 |
rs191935439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936330 | GTCAAAAGCTATAAA[A/G]TGTCATCCCTGGGAG | 83860 |
rs191937604 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7954126 | TCCATAGGTGAATGA[A/G]TGAATTAGTCCCAGT | 83860 |
rs191958138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895076 | AGACAGAGTTTCACC[A/G]TGTTTGCCAGGCTCC | 83860 |
rs191967589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7879401 | TATTTTATCTCATAA[A/G]GTTTTGAGTCAGAAC | 83860 |
rs191985626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915842 | AAATTAGCTGGATTT[G/T]GTGGTGGGCACCTGT | 83860 |
rs192009128 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7873190 | TTTAAATCTTTAATC[A/G]ATAGCCATATCAAAT | 83860 |
rs192017130 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7907167 | ACACGCTGGATCTCC[G/T]GGAGTTGAAAGTAGG | 83860 |
rs192044081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839259 | GTATAATATATATCT[A/C]TACCATCATACTTCA | 83860 |
rs192058896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006444 | GCCTGGCCCACAATT[A/G]GCTTTCAAGTGCTTA | 83860 |
rs192078859 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7947487 | GCAGTGGCAATGAGG[A/C]CAGGTAAGAAAGCTA | 83860 |
rs192096790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978802 | TATTCCCATGTCTCA[C/G]TAACTCACCATTACT | 83860 |
rs192100343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7985176 | GTGGTAGCCACAAGT[C/T]TCAGCATGTGGAACT | 83860 |
rs192104188 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7950002 | TAATAAATTAGAGTC[A/C]ATGATACATGGTGAA | 83860 |
rs192105934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999742 | GATTACAGGCGTGAG[A/C]CACCGTGCCCAGCCC | 83860 |
rs192122607 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7891756 | AGCTTTGAGCTCTTA[A/G]GGTAAAACACATCAT | 83860 |
rs192136565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957863 | ATTATTATTATGTCT[A/G]TATTTGTGTTAAAGT | 83860 |
rs192140610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7932292 | AATTCTCTTTTCCCC[A/G]CTTCTTGGAAAACAC | 83860 |
rs192140872 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7910586 | GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTCC | 83860 |
rs192142536 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7856346 | CCAGGAGTGGTGGTG[C/T]GTGTGTACCTGTAAT | 83860 |
rs192179837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7820872 | ATCACCAGCTGACTA[C/T]TCTTCTGGCTTTTGT | 83860 |
rs192191343 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920455 | CTTTTTATGCTTTGC[A/G]TTTTGTTCTGCAATT | 83860 |
rs192197579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7959658 | TGAGCTCTAAATTCA[A/T]AGTAAACCAATATAT | 83860 |
rs192209343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850423 | GCTCATGCCTTTAAT[C/T]CTAGCACTTTGGGAG | 83860 |
rs192257637 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:8000612 | TCTCTACACACAAAA[A/C]AATACGTATACAAAA | 83860 |
rs192349367 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7889422 | TGTAAGGCAAATACT[A/G]TTCACATCTGTCTGT | 83860 |
rs192391916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855492 | AGCCATTTCTTCATC[C/T]TTTGGGGAGGAGATT | 83860 |
rs192404538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7825671 | CTGTGTCGGGATTTC[A/G]TTGTGTGTTTCGTTG | 83860 |
rs192441483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7928674 | TGTTGTAATGGTTTT[C/T]CTATTCCTTCTGGGG | 83860 |
rs192449485 | snp | A/C/T | 0.00011659 | 0.00763422 | missense, synonymous-codon | TAF3 | GRCh38.p7 | 10:7965476 | GCACCCCCACTGGTG[A/C/T]TGCCCCCAAAAGAGT | 83860 |
rs192470823 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861166 | AGATTGGGTTTCACT[A/G]TGTTAGCCAGGGTGG | 83860 |
rs192484492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7843480 | AGTTGTAGTCATCTA[C/T]AGGTTTAAGTAACTT | 83860 |
rs192492718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997941 | GTTTATCTCACAAGT[C/G]ATGAAAAATTATATC | 83860 |
rs192493707 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887593 | TTTCCTAGTGATAAG[C/T]GTGAACTGTTTAGGC | 83860 |
rs192539334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875390 | ACTTAGCCATTTCTC[C/T]TTCTGGCTGAATAGT | 83860 |
rs192555539 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7840085 | ATTTAAGGGATTGAA[A/C]AATTTTTTTTTTAAG | 83860 |
rs192556363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821279 | TAGATTCTTTTTTCT[A/G]TACCAGCCTTATTCT | 83860 |
rs192570942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865348 | GCCAGGTATGGTGGC[A/G]GGCGCCTGTAGTCCC | 83860 |
rs192573800 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7846237 | GCTGGCATTACAGGC[A/G]TGAGCCACTGCGCCC | 83860 |
rs192596018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7941607 | CTCACTGTATCCTCA[C/T]CATCCTGGACATCCT | 83860 |
rs192639187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883476 | GACTTCCAGATTTCT[C/T]CATTGTCAAGTTATT | 83860 |
rs192641272 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7840477 | GTGTTTTGATATTTA[C/T]TATAAACACCAAATT | 83860 |
rs192641582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010633 | TAAAACCAGCTGGAC[A/G]CAGTGGCTTACGCCT | 83860 |
rs192657462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979161 | CATCCTGTCTAACAC[A/G]GTGAAACCCCTTCTC | 83860 |
rs192667319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8001149 | CCAGACCTTTACACA[A/G]CTGTCTAATGTTGCC | 83860 |
rs192687151 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900357 | AATCATTCTTATAAG[A/G]AAACATATGATAATG | 83860 |
rs192697896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865439 | AGCCGAGATCGCGCC[A/T]CTGCACTCCAGCCTG | 83860 |
rs192703702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831636 | GGAGTGAGCTACCGT[C/G]CCCGGCCTCATTACA | 83860 |
rs192723402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953192 | CGGTTCCATTTTCCC[A/C]GTCTTCTCACTTCAA | 83860 |
rs192758702 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7880075 | ATTAGCTGGCCACCC[A/C]AAAAATATAACAAAT | 83860 |
rs192761757 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7943976 | TACTTTGAAAAGGGG[A/G]TGGGTTTTCTTGTTC | 83860 |
rs192762652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916193 | CTTTCAGTGAGCTAG[A/G]CAGTTTCCTTTGTTA | 83860 |
rs192767637 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7844627 | GTGATCCGCCTGCCT[C/T]GGCCTTCCAAAGTGC | 83860 |
rs192795498 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7982916 | TGCTGACAGCTCTTA[A/T]GCACCTCTTCATCTC | 83860 |
rs192821127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826107 | CTGTGTGTCAGGGTT[G/T]CCTCATCTGAAAAAC | 83860 |
rs192866678 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994808 | TCTCTACTAAAAATA[A/C]CAAAAAAAAAAAAAA | 83860 |
rs192869554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963773 | TGTAACAAACCTGCA[G/T]GTTGTGCCCATGTAC | 83860 |
rs192890418 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884195 | ATACTCCTTTACTGT[G/T]ATTATTTATTTCACT | 83860 |
rs192901813 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7846965 | AGATTAAAAAGGACT[A/G]GAAACACCTTCTTTT | 83860 |
rs192910166 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969493 | GTTGGTGTATATATT[A/G]CATGGATCTTTGGGG | 83860 |
rs192920482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7940620 | TTATTATTTGAGACA[C/G]TTCTTGTAAAGTAGA | 83860 |
rs192944923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010938 | TTGTAAATCCCACCA[C/T]GTCCACTGAGTCCAC | 83860 |
rs192962891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926806 | TAAGATTAGTAAGCA[A/G]TAGTTTTTAAACTTT | 83860 |
rs192973013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7895696 | TGAGACTTTCCATTG[A/C]ACACATTTTTTTCCA | 83860 |
rs192973030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963202 | AAAATACCTGTCATT[C/T]CTGATAATAATAATA | 83860 |
rs192982600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862382 | TTTTTGTTTCAGCAG[A/G]AAGTTACCTTAGTTC | 83860 |
rs192983575 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7826747 | AGATGCTTGTCAAAA[C/T]GTTCTCCTCTTCATA | 83860 |
rs193008080 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:8004599 | GCACATTGAAGATGT[C/T]ATTCCACTATCTTCT | 83860 |
rs193033876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7836433 | GCATGAGCTACCAAG[C/G]CCAGCTAATTTTGTA | 83860 |
rs193046337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972933 | GACAAATAAAGTGAA[C/T]AGCTCCATGTAAGCC | 83860 |
rs193074498 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7945660 | TGTCCCAGCAGCAAG[A/G]GTGTGCCCTTGCTCC | 83860 |
rs193077605 | snp | A/G | 0.00103815 | 0.0227595 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8014700 | CTGCCCCAAGTGTGC[A/G]AACAAGAAGAAGGAC | 83860 |
rs193078230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7870481 | TGCCTGATGGAAGAT[A/G]CTTTCTGGTGGTTCA | 83860 |
rs193082915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894646 | TTTATTGAACACTTA[C/G]TATAAATGCCAAAAT | 83860 |
rs193088114 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7935968 | ACTCTCGAGTCTCAT[G/T]TGGGCTGCCGATTGT | 83860 |
rs193091658 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837357 | AAAAAAAAAAAAAAA[A/G]GTCAGCTGGGTGTGG | 83860 |
rs193125711 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7910087 | TTGTTACTTTTATTG[G/T]TTTTTTCCCCTCAAA | 83860 |
rs193137131 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7875903 | ATTTTTTTCTTGTAC[G/T]ACTAATTTTACCGAC | 83860 |
rs193145871 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7949485 | CTAGCCTTTCCCTTT[C/G]CATCGCATTATGTAA | 83860 |
rs193151252 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7989370 | AAACCCAGCAGATGC[C/T]CTGAGCCTAGACCTC | 83860 |
rs193162736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919389 | GAAATCTTGCAGGGT[A/G]TACTGTCCTGGTGTT | 83860 |
rs193173893 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990185 | CTTGATCTGTATATG[A/T]ATACGTGAGTTCTGC | 83860 |
rs193243727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7853106 | TGAGAGTGAGTTGGC[A/G]AATGTTGTTTAATAT | 83860 |
rs193246101 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914604 | AATTTTATTTCATAT[G/T]ATGTTTGCATTTTGA | 83860 |
rs193251826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879019 | AGGCATAAGTCACCG[C/T]GCCTGGCAAATTCAA | 83860 |
rs193253339 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817736 | GGACACTCGGCCTGC[A/G]ACACCGGTTTAAGGC | 83860 |
rs193268965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831067 | TCCATTAATTCATTA[A/G]GGGTTACAAAGTAAT | 83860 |
rs193280122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891538 | ACAGCAAATTTTTTG[A/T]AAACAGTTTTTTCTG | 83860 |
rs193284213 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930980 | AAATCTGTGCTGCAC[A/G]CTATAAATAGAACAA | 83860 |
rs193284980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858381 | AGTTTTTCTTCCTGG[C/T]GCTTGATCCTTTAGA | 83860 |
rs193298876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968330 | TCGGCAAGCAAGAGC[A/G]TTTGTTTAAATTTTT | 83860 |
rs199497720 | snp | C/T | 0.000334638 | 0.0129309 | missense | TAF3 | GRCh38.p7 | 10:7964990 | TTTCCTTATATCTCT[C/T]CTCCGTCAGTGTCTC | 83860 |
rs199509962 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841287 | TTCGTCAAGGAGCTG[G/T]GGAGAGCCTGCTGTC | 83860 |
rs199510877 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887249 | AAAAAAAAAAAAAAA[C/T]AAAGAAAGCTGGTTA | 83860 |
rs199551155 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939578 | AAATAGAAGAAAACT[-/AC]ACACACACACACACA | 83860 |
rs199583526 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888510 | GCATGAGATCTTCTA[A/C]AGAAGATGTGGAGGT | 83860 |
rs199604543 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974220 | TATGCAAGGGTCTTG[C/T]TCCACCCGCCACCCA | 83860 |
rs199621862 | snp | A/G | 0.000104771 | 0.00723701 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965172 | CAAGGACAAAAGTAA[A/G]GAGAAGGATAAAGTG | 83860 |
rs199623487 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883505 | TTACTTTCTCCTTTG[C/T]CATTGATAGCTATCT | 83860 |
rs199628830 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954408 | AATGAGTGAATTAGT[C/T]CTAGTTAACACGAGC | 83860 |
rs199635542 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7967282 | CTCAGTAAATCAAAC[-/AG]GGGACTGTTCCTGTC | 83860 |
rs199655446 | in-del | -/A/TTTTTTTTTTTTT | 0.0926964 | 0.194308 | intron-variant | TAF3 | GRCh38.p7 | 10:7884392 | AAGAGCTCTGCCTCC[-/A/TTTTTTTTTTTTT]TTTTTTTTTTTGAGA | 83860 |
rs199655950 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938544 | ACTGAGAGAATTTGA[-/A]CGGCCAGTCAGACAA | 83860 |
rs199706438 | in-del | -/ACAA | 0.188 | 0.24219 | intron-variant | TAF3 | GRCh38.p7 | 10:7959162 | CACACACACACACAC[-/ACAA]AAAAAGTTTCAGGCT | 83860 |
rs199755167 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857927 | TTTTTTTTTTTTTTT[C/T]TGCTAACCTTAGGGA | 83860 |
rs199762284 | in-del | -/C | 0.442151 | 0.159931 | intron-variant | TAF3 | GRCh38.p7 | 10:7824305 | ATTTGATTTGCTTTT[-/C]ACTTTGTTTCAGATG | 83860 |
rs199768404 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998778 | CAGGAGGTGGAGGTT[G/T]CAGTGAGCCGGGATC | 83860 |
rs199775696 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012243 | CGCTTTGTGGTTAGA[A/G]GACAAAATTTATGAT | 83860 |
rs199786009 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946727 | GACCCTGGTCTCAAA[A/C]GAAAAAAAAAGAAGG | 83860 |
rs199790154 | in-del | -/AATA | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7900884 | CTTTTTAAAAATCAT[-/AATA]AATTTATCACAAAAC | 83860 |
rs199800802 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881490 | ACACACATACACACA[A/C]ACACACACACACACA | 83860 |
rs199887987 | in-del | -/A | 0.0733688 | 0.176922 | intron-variant | TAF3 | GRCh38.p7 | 10:7987316 | GTGAGAACCTGTCTC[-/A]AAAAAAAAATAAAAA | 83860 |
rs199892027 | snp | G/T | 0.00199792 | 0.0315431 | intron-variant | TAF3 | GRCh38.p7 | 10:8009031 | GCACGGGTTTGGTTC[G/T]ATGATGATCCTGTTT | 83860 |
rs199903848 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861178 | ACTGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT | 83860 |
rs199942319 | snp | C/T | 0.00175939 | 0.0296074 | missense | TAF3 | GRCh38.p7 | 10:8009287 | GGGCCAGTGCCAAAG[C/T]CCCCGTGCGCAGCGT | 83860 |
rs199956734 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926265 | TTTAATATATCAAAC[-/T]TTTTTTTTTATTACG | 83860 |
rs199965942 | in-del | -/AATAAATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859261 | GTGAGACTCCATCTC[-/AATAAATA]AATAAATAAATAAAT | 83860 |
rs199968424 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869246 | CTTCCTGACTTCTAC[C/T]GTGTGTGTGTGTGTC | 83860 |
rs199972101 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845318 | TCTTTGTGTGTGTGC[-/GT]GTGTGTGTGCACACG | 83860 |
rs199979028 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872234 | CTACTGGGAAAGAAA[A/G]AAAAAAAAAAAAAAA | 83860 |
rs199994712 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901010 | TTCTGGTGTGCTTGT[A/G]GTGATCATCCAAAAA | 83860 |
rs200013312 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015044 | TTATTAATAAAGAGC[A/G]TACATCTTCCCTTTT | 83860 |
rs200016262 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969147 | TCTCTCCAAAACAAA[A/C]AAACAAACAAACAAA | 83860 |
rs200028242 | in-del | -/A | 0.31357 | 0.241783 | intron-variant | TAF3 | GRCh38.p7 | 10:7953877 | AGTCCTAGTTAACAC[-/A]GAGCTCTCCATAGTG | 83860 |
rs200029651 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996645 | TTGTTGTGAGGGGGG[-/T]TTTTTTTTGTGTTAT | 83860 |
rs200030488 | snp | G/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817413 | ATGTGAATATCATGT[G/T]CAAAGTTCTGGAATA | 83860 |
rs200035612 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7959585 | AAGCTTAATGTTAAG[-/T]TTTTTTTACTGAAAC | 83860 |
rs200045830 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7916625 | AATAGGTGAGCTTTT[-/A]AAAAATAAAGTGTAT | 83860 |
rs200052475 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959140 | ACGAGATTCTGTCTC[A/T]CACACACACACACAC | 83860 |
rs200090418 | in-del | -/TGTGTGTGTGTGTGTGTGTGTGTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920309 | ACATACGTGTGTGTG[-/TGTGTGTGTGTGTGTGTGTGTGTA]TGTGTGTGTGTGTGT | 83860 |
rs200106163 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860419 | TGCCCCATCCCAATC[A/C]CAGCCTCTTCTTTCC | 83860 |
rs200118262 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | TAF3 | GRCh38.p7 | 10:7824456 | CGTCATTTCCTGTTA[A/G]CAAGAACAATGTACT | 83860 |
rs200140973 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817418 | AATATCATGTTCAAA[C/G]TTCTGGAATAGTCCC | 83860 |
rs200160855 | snp | G/T | 0.0912534 | 0.193131 | intron-variant | TAF3 | GRCh38.p7 | 10:7884402 | GCCTCCTTTTTTTTT[G/T]TGAGATGGAGTTTTG | 83860 |
rs200180608 | in-del | -/AGATGTCTTCTGCCCAAG | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7899280 | CTCCTTCCCTTCCCC[-/AGATGTCTTCTGCCCAAG]GGAAGAAGGAATCGC | 83860 |
rs200191736 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850683 | CATCTCAAAAAAAAA[-/T]AAAATATATATGTAT | 83860 |
rs200252587 | in-del | -/AG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935624 | AAGCTAAAGCTAAGT[-/AG]AGGGCCAGAGAATAC | 83860 |
rs200282652 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836289 | CACGTTTTCTTTTTT[C/T]TTTCTTTTTTTTTTT | 83860 |
rs200284646 | in-del | -/AAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846615 | TTCCTAGAGGCTAAC[-/AAAA]AAAAAAGGAGAAAAA | 83860 |
rs200288449 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881492 | ACACATACACACAAA[A/C]ACACACACACACACA | 83860 |
rs200289162 | in-del | -/ATGTTCAAAG | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817409 | AAAAATGTGAATATC[-/ATGTTCAAAG]TTCTGGAATAGTCCC | 83860 |
rs200318655 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994226 | TTCTTACTTTCTGGT[-/A]AAAAAAAAATTCCAG | 83860 |
rs200321191 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935301 | ATAAATAAATAAATA[A/G]AAGAAAAATAAAGCG | 83860 |
rs200323637 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843646 | TATCTCTTTCTCACT[C/T]TTTTTTTTTTTTTGA | 83860 |
rs200326785 | in-del | -/ATGTATGTATGTATGTATGTATGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878691 | TAATTAATTCAACCA[-/ATGTATGTATGTATGTATGTATGT]ATGTATGTATGTATG | 83860 |
rs200334732 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838366 | CCAGTTTTGTTTTTT[G/T]TTGTTGTTGTTGTTT | 83860 |
rs200334894 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881252 | CTCAAAAAAAAAAAA[A/C]AAAAAAAAAACCCAC | 83860 |
rs200336928 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925814 | AAAAAAAAAAAAAAG[A/G]AAAGAAAAGAAAAGA | 83860 |
rs200355016 | in-del | -/ACAA | 0.0205511 | 0.0992634 | intron-variant | TAF3 | GRCh38.p7 | 10:7910324 | ATACTGCTACAACAT[-/ACAA]ACATCTAAATATCAG | 83860 |
rs200361154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825491 | TAAACATAACTCCCC[A/G]TTCTCCACCACTTCC | 83860 |
rs200412133 | in-del | -/T/TTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838359 | ACCAAGCCAGTTTTG[-/T/TTT]TTTTTTTTTGTTGTT | 83860 |
rs200419391 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959139 | AACGAGATTCTGTCT[-/CA]CACACACACACACAC | 83860 |
rs200425089 | in-del | -/TC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825967 | GCTTCCTATCAGCAG[-/TC]TGCCCAAGGGTTCCA | 83860 |
rs200425852 | in-del | -/A | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015868 | AGTAAAAAAAAAAAA[-/A]CAACAAAAAACCCAC | 83860 |
rs200436429 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936511 | ATCTTTTTTTTTTTT[C/T]CTTAATAGACTTTAT | 83860 |
rs200457204 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963788 | TGTTGTGCCCATGTA[C/T]CCTAGAACTTAAAGT | 83860 |
rs200457802 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7864465 | CACTCTCTACATTTT[-/A]AAAAAAATACTACAG | 83860 |
rs200463698 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7971455 | TACATATATGGTGTT[G/T]TTTTTTTTTTTTAAT | 83860 |
rs200464075 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009438 | TCTCTTCAAAATTTT[A/G]TTATTTACTTAATTA | 83860 |
rs200501611 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864833 | TTATCTTTTTTTTTT[C/T]CCTTTTTATGTTTTG | 83860 |
rs200505424 | snp | A/G | 0.00384383 | 0.0436708 | missense | TAF3 | GRCh38.p7 | 10:8009265 | TCCCCGGGTCCCGCC[A/G]CCTCCGGGGCCAGTG | 83860 |
rs200509928 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923590 | TGTATAGCAAAAAAA[-/C]AAAACAAAACAAAAC | 83860 |
rs200516205 | in-del | -/TTATTAAAAATTA | 0.0505692 | 0.150756 | intron-variant | TAF3 | GRCh38.p7 | 10:8014074 | GCTTATCTATCCTTC[-/TTATTAAAAATTA]TTATTAAAAATAATA | 83860 |
rs200545294 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7822255 | GGTTAAAAAAAAAAA[A/G]AAAAGGTGGCCGAAG | 83860 |
rs200550840 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936499 | GACCTGAGCTGCATC[-/T]TTTTTTTTTTTTCTT | 83860 |
rs200591560 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988752 | AGATTCTGTCTCTCA[A/G]AAAAAAAAAAAAAAA | 83860 |
rs200607141 | in-del | -/TTAT | 0.0766824 | 0.180169 | intron-variant | TAF3 | GRCh38.p7 | 10:7832543 | TTTATCATTTCTTTC[-/TTAT]TTATTTATTTATTTA | 83860 |
rs200610326 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857784 | TGATGTTTTTGTTAA[-/G]GAAAGAAAAAGGCAG | 83860 |
rs200613506 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844378 | CTTCTTCTTCTTGTT[C/T]TTTTTTTTTTTTTTT | 83860 |
rs200659533 | in-del | -/TCTC | 0.0197687 | 0.0974348 | intron-variant | TAF3 | GRCh38.p7 | 10:8003207 | TTCAGTGGTTTTTTT[-/TCTC]TCTCTCTCTTTTCTT | 83860 |
rs200667450 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863648 | ATATATATATATATA[C/T]ACACACACATATATA | 83860 |
rs200672481 | snp | A/G | 1.6782e-05 | 0.00289668 | missense | TAF3 | GRCh38.p7 | 10:7965030 | CCGAACCTCTCCACA[A/G]GGTGTATGAGGAGAA | 83860 |
rs200672495 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849187 | ATTATCTTTTTTTTT[-/T]CTTATAGATGAGGGA | 83860 |
rs200686520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819870 | ATTTCTTAGGCCCCA[A/G]GTTTCGTTCCCGCTT | 83860 |
rs200707169 | in-del | -/CAAGAGTG | 0.0596104 | 0.162024 | intron-variant | TAF3 | GRCh38.p7 | 10:8014008 | ATTAACTGCAAAACC[-/CAAGAGTG]CTTAGACTATTGTTA | 83860 |
rs200710627 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842163 | ATTGTTTTTTTTTTT[G/T]GTTTTTTTTTTTGTT | 83860 |
rs200753513 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881252 | CTCAAAAAAAAAAAA[-/C]AAAAAAAAAACCCAC | 83860 |
rs200809294 | snp | C/T | 0.000868418 | 0.0208196 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7977303 | ATTAACTCTCCGAGT[C/T]GGTGCTGGCCAAGAC | 83860 |
rs200827611 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888511 | CATGAGATCTTCTAA[A/T]GAAGATGTGGAGGTC | 83860 |
rs200831062 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841650 | TAGTCACCCAAGGGA[C/G]ATGATAGGAAGGACC | 83860 |
rs200842950 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925427 | CAATGGTAATATGGA[G/T]GTGTTAACCTCTTTT | 83860 |
rs200849436 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959163 | ACACACACACACACA[A/C]AAAAAAAGTTTCAGG | 83860 |
rs200853732 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | TAF3 | GRCh38.p7 | 10:7957872 | ATGTCTATATTTGTG[-/T]TAAAGTAGAAAGGGC | 83860 |
rs200853774 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901011 | TCTGGTGTGCTTGTG[C/G]TGATCATCCAAAAAT | 83860 |
rs200854513 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838365 | CCAGTTTTGTTTTTT[-/G]TTTGTTGTTGTTGTT | 83860 |
rs200868570 | snp | C/T | 3.59557e-05 | 0.00423988 | missense | TAF3 | GRCh38.p7 | 10:8009116 | CCCCCGAGGCCAAGC[C/T]GGCGCCCTCGCAGAA | 83860 |
rs200884598 | snp | A/C/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846619 | CTAGAGGCTAACAAA[A/C/G/T]AAGGAGAAAAATGAT | 83860 |
rs200893179 | snp | A/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817419 | ATATCATGTTCAAAG[A/T]TCTGGAATAGTCCCT | 83860 |
rs200905669 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869261 | CGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTCT | 83860 |
rs200922557 | in-del | -/CGCTCTCTCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957793 | ACGCTCTCTCTAGCG[-/CGCTCTCTCT]CTCTCTCTCTCTCTC | 83860 |
rs200924421 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979361 | AAAATGAAAAAAAAA[A/T]GAAAAAAAAAAAAAA | 83860 |
rs200955964 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873756 | ACATGACAGAGGCTG[G/T]CCTAGTTCCTTGATT | 83860 |
rs200965415 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878729 | TATGTATGTATGTAT[A/G]TATGTATGTATGTAT | 83860 |
rs200975196 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817414 | TGTGAATATCATGTT[C/G]AAAGTTCTGGAATAG | 83860 |
rs201000913 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948066 | ACTTTATGACTCTGA[-/T]TTTTTTTTTTTTTGG | 83860 |
rs201008368 | in-del | -/T | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:8001458 | TAAGAACATTAATTC[-/T]TTTTTTATTCACAAC | 83860 |
rs201021566 | in-del | -/CACTGCA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828989 | CAGCCGAGATCGTGC[-/CACTGCA]CTCCAGCCTGGGTGA | 83860 |
rs201022301 | in-del | -/AAAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983871 | AATAAATAAATAAAT[-/AAAT]TTTTAAAAAGCAAAA | 83860 |
rs201035999 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967237 | TTAGTCATTTATCCC[C/T]TGTGTACCTAGTAAG | 83860 |
rs201044629 | in-del | -/TTTC | 0.0283406 | 0.115616 | intron-variant | TAF3 | GRCh38.p7 | 10:7988793 | TTATCAAGTAGGCAT[-/TTTC]TTTGTTTTTTATTTT | 83860 |
rs201092119 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840088 | TAAGGGATTGAAAAA[-/T]TTTTTTTTTAAGTTT | 83860 |
rs201095393 | snp | A/C/G | 4.97775e-05 | 0.00498866 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964830 | AGCTTCCACTTCCGC[A/C/G]AACAATTTCACAAAG | 83860 |
rs201095581 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898814 | TTTGTTTTCTTTGAG[-/T]TTTTTTTTTTCTCTT | 83860 |
rs201158850 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886218 | ACAGGTGTAAGACAC[C/T]ACACCTGGCCCTGTT | 83860 |
rs201160637 | in-del | -/AG | 0.0103295 | 0.0711199 | intron-variant | TAF3 | GRCh38.p7 | 10:7974110 | TCCAGCCTGGGCGAC[-/AG]AGTGAGATTCCTTCT | 83860 |
rs201175909 | in-del | -/AG | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7960358 | TGGTAGGTCTAGGAC[-/AG]GGGTCAGCAAACGTT | 83860 |
rs201201879 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | TAF3 | GRCh38.p7 | 10:7919111 | AGGGTACAGAATCTG[-/A]AAAAAAAATGGGAGA | 83860 |
rs201204620 | snp | A/C | 1.66098e-05 | 0.00288177 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964275 | TCCAGTTGCAAAATC[A/C]CAAATGCCAACTGCA | 83860 |
rs201220071 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872213 | AGAAGTGTTGGGTTG[A/T]TTTTTTTTTTTTTTT | 83860 |
rs201229918 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860277 | CCAGACCCTGTCTGG[-/A]AAAAAAAAAGAAGAA | 83860 |
rs201250594 | snp | A/G | 0.415399 | 0.187465 | intron-variant | TAF3 | GRCh38.p7 | 10:7998267 | TATATATATATATGT[A/G]TATATATATATATAT | 83860 |
rs201271247 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826449 | TTTAGTGTTTTTTTT[G/T]TTTTGTTTTGTGTTG | 83860 |
rs201276522 | in-del | -/ATGTATGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878691 | TAATTAATTCAACCA[-/ATGTATGT]ATGTATGTATGTATG | 83860 |
rs201281091 | in-del | -/CA | 0.0260105 | 0.111035 | intron-variant | TAF3 | GRCh38.p7 | 10:7867253 | ACACACACACACACA[-/CA]AAAAACAAAAAACAA | 83860 |
rs201305416 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990038 | CAGTTAAAATTAACT[A/G]TATCTATTTTTAAGA | 83860 |
rs201318527 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925544 | CACAGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 83860 |
rs201338448 | snp | C/G/T | 6.68733e-05 | 0.00578211 | synonymous-codon, missense | TAF3 | GRCh38.p7 | 10:7963996 | CTTGGAAGAAGATGA[C/G/T]GAATTGGAGGAGGAA | 83860 |
rs201347117 | in-del | -/CACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959159 | ACACACACACACACA[-/CACA]CAAAAAAAGTTTCAG | 83860 |
rs201354485 | in-del | -/CTT | 0.0341408 | 0.126114 | intron-variant | TAF3 | GRCh38.p7 | 10:7941620 | ATCATCCTGGACATC[-/CTT]CTTGCTGCGCCGATG | 83860 |
rs201370190 | in-del | -/TGTGTGTGTGTGTGTGTGTGTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920311 | ATACGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTGTGTA]TGTGTGTGTGTGTGT | 83860 |
rs201373329 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958493 | AATTAAAAAAAAAAA[-/A]TTATAGTATCATACT | 83860 |
rs201388257 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974026 | CCAGCTACTCGGGAG[G/T]CTGAGGCAGGAGAAT | 83860 |
rs201392717 | in-del | -/AGAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822192 | CTTGAGACTATACTG[-/AGAT]AGTGACAGTAAGAAT | 83860 |
rs201404309 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001390 | TTGTCTAGTGGCTGG[G/T]TTTGGTTTTTTTATT | 83860 |
rs201425540 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979363 | AATGAAAAAAAAATG[-/AA]AAAAAAAAAAAAGGC | 83860 |
rs201442827 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985820 | ACGGAATCTCACTCT[C/G]TGGCCCAGGCTGAAG | 83860 |
rs201459246 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864835 | ATCTTTTTTTTTTTC[C/T]TTTTTATGTTTTGTA | 83860 |
rs201464808 | snp | A/G | 0.000233139 | 0.0107942 | missense | TAF3 | GRCh38.p7 | 10:7964375 | AAATCACCTAAAACC[A/G]CCCAGTCACCAGCAA | 83860 |
rs201498412 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947359 | TTAGGCGCTGTTTAG[A/T]CTCTGGGAATAGTCT | 83860 |
rs201498517 | in-del | -/G | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7935765 | TTCCAAAGAGAGGAA[-/G]GCGCAGATTCCAGGC | 83860 |
rs201526218 | in-del | -/TCTC/TCTCTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957793 | CGCTCTCTCTAGCGC[-/TCTC/TCTCTC]GCTCTCTCTCTCTCT | 83860 |
rs201540307 | in-del | -/ACACACACACACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939578 | AAATAGAAGAAAACT[-/ACACACACACACACACAC]ACACACACACACACA | 83860 |
rs201544792 | in-del | -/ACACAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959160 | CACACACACACACAC[-/ACACAA]AAAAAGTTTCAGGCT | 83860 |
rs201551451 | snp | G/T | 0.188316 | 0.242271 | intron-variant | TAF3 | GRCh38.p7 | 10:7845965 | TGTGTTTTTGTTTTT[G/T]TTTTTTTTTTTTGAG | 83860 |
rs201617646 | in-del | -/TAAGT | 0.0368353 | 0.130617 | intron-variant | TAF3 | GRCh38.p7 | 10:7910987 | CTTAACCTTAGCTTC[-/TAAGT]TAAGTGTCTTTGATA | 83860 |
rs201655461 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871498 | GCCCAGGCTAGAGTG[A/C]AATGGTGTGATCTCT | 83860 |
rs201660949 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869245 | CCTTCCTGACTTCTA[C/G]CGTGTGTGTGTGTGT | 83860 |
rs201684970 | snp | C/T | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:8013775 | GATCTGCCCTGGGTG[C/T]AACAAGCCTGACGAT | 83860 |
rs201709104 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946717 | GACAGAGTAAGACCC[-/T]GGTCTCAAACGAAAA | 83860 |
rs201712983 | snp | C/G/T | 4.53669e-05 | 0.0047625 | missense | TAF3 | GRCh38.p7 | 10:8014699 | TCTGCCCCAAGTGTG[C/G/T]GAACAAGAAGAAGGA | 83860 |
rs201724013 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958158 | GTGGTAGAGGCTAAA[-/CA]GTTCAATAGCCATTA | 83860 |
rs201730829 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946723 | GTAAGACCCTGGTCT[A/C]AAACGAAAAAAAAAG | 83860 |
rs201738649 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979363 | AATGAAAAAAAAATG[A/G]AAAAAAAAAAAAAGG | 83860 |
rs201772654 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964209 | TTCTCCAGTCCATGT[A/G]CAGGACAGTACAGAC | 83860 |
rs201795993 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863694 | ATATATACACACACA[C/T]ATATATATATACACA | 83860 |
rs201820107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834663 | ATGTTACATCCATAA[A/G]TACTGTCATCCATAC | 83860 |
rs201830978 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888512 | ATGAGATCTTCTAAA[A/G]AAGATGTGGAGGTCT | 83860 |
rs201834884 | in-del | -/AG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925812 | TCAAAAAAAAAAAAA[-/AG]AAAAGAAAAGAAAAG | 83860 |
rs201837896 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817411 | AAATGTGAATATCAT[C/G]TTCAAAGTTCTGGAA | 83860 |
rs201841378 | snp | A/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817417 | GAATATCATGTTCAA[A/T]GTTCTGGAATAGTCC | 83860 |
rs201867529 | in-del | -/CA | 0.0267878 | 0.112589 | intron-variant | TAF3 | GRCh38.p7 | 10:7942746 | GCCGAGGCGTGTGGG[-/CA]CGGAGTTCTAGATCT | 83860 |
rs201872212 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001394 | CTAGTGGCTGGTTTT[G/T]GTTTTTTTATTCTAT | 83860 |
rs201897666 | in-del | -/AA | 0.479904 | 0.0982045 | intron-variant | TAF3 | GRCh38.p7 | 10:7823946 | AAGATGCCATCTCTT[-/AA]AAAAAAAAAAAAAGA | 83860 |
rs201905198 | in-del | -/AAAAAAAAAA | 0.488057 | 0.0763479 | intron-variant | TAF3 | GRCh38.p7 | 10:7898546 | ACAAGACTCTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 83860 |
rs201912372 | snp | A/C | 0.000624351 | 0.0176575 | intron-variant | TAF3 | GRCh38.p7 | 10:7977231 | AACTTTAATGTGCTA[A/C]CTTCCACAGATAAAA | 83860 |
rs201926858 | in-del | -/AATAAATAAATAAATAAATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859261 | GTGAGACTCCATCTC[-/AATAAATAAATAAATAAATA]AATAAATAAATAAAT | 83860 |
rs201933001 | snp | G/T | 0.039522 | 0.134904 | intron-variant | TAF3 | GRCh38.p7 | 10:7954383 | AGATTCAGAGTGCAC[G/T]CCATAGGCAAATGAG | 83860 |
rs201944746 | in-del | -/CC | 0.0825414 | 0.185628 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817831 | AATCGCACACTATAG[-/CC]CACAGGCAGCTTACC | 83860 |
rs201949310 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933395 | TGAGGAAGGGAAATA[A/T]CCAGTGTGGAGCCAA | 83860 |
rs201956997 | snp | A/G | 0.000798788 | 0.0199689 | missense | TAF3 | GRCh38.p7 | 10:7964025 | AAGAAATTATTAATG[A/G]TGAGAATTTCCTGGG | 83860 |
rs201963985 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837357 | AAAAAAAAAAAAAAA[-/G]GTCAGCTGGGTGTGG | 83860 |
rs202011792 | in-del | -/GTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838380 | TTTGTTGTTGTTGTT[-/GTT]TGTTTGTTTGTTTGT | 83860 |
rs202051795 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014617 | AAAAGTTGCTTATCT[A/G]AGCTTGTTTTCACGT | 83860 |
rs202086503 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937640 | CATAGTCTGTGGCTT[A/C]TCTTTTCCTCACAGT | 83860 |
rs202099081 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920890 | TAAAAAGCTGTTGCT[A/G]GTTTCCCAAATCTTA | 83860 |
rs202117825 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877042 | ACTTTTTTTTTTTTT[A/G]CTAATGGAGATTCCA | 83860 |
rs202119556 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933110 | AAACAAAAAAAAAAA[-/T]ACCTGGCTACTTTGA | 83860 |
rs202172490 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | TAF3 | GRCh38.p7 | 10:7824581 | TGAGTGTTTCTTCTT[C/T]ATATGTTAGTGATTA | 83860 |
rs202181834 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907340 | GCCCAAAGTGTGCTG[-/T]TCCTATCCTTGCTGG | 83860 |
rs202185221 | snp | C/T | 3.36395e-05 | 0.00410105 | missense | TAF3 | GRCh38.p7 | 10:7963979 | GAAGCCATGCAGGTT[C/T]CCTTGGAAGAAGATG | 83860 |
rs202202772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7856902 | AGAATGCTTCACAAG[C/T]TTATTTTACTAACAT | 83860 |
rs202214813 | in-del | -/CAAACTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009525 | AGCTCACTGCAACCT[-/CAAACTC]CTGGGCCCAAGCGAT | 83860 |
rs367547760 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827299 | AATAACACCTACCAC[A/G]TTGGGGAAATGGAGA | 83860 |
rs367562133 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825204 | TGGTCTCTAACACAA[A/G]TACACGATATTTTTT | 83860 |
rs367595230 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:7967339 | AGTGGAGTTGTTTCA[A/C]CAGCCATTATGAATT | 83860 |
rs367608369 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936067 | GTCCTGGACTAGTGT[A/G]ATTGTATCGTAAAAC | 83860 |
rs367656886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011098 | TGTGGAGCCATTGCC[A/T]TTGCTGTGACTACCA | 83860 |
rs367673372 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993656 | AAGTTCATTCTTTTT[C/T]TCTTAAAGGGTATTT | 83860 |
rs367674988 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002605 | TTTTAGCCTTAAGAA[A/G]TTGGGTCAGTTTCTT | 83860 |
rs367676547 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859276 | AATAAATAAATAAAT[A/C]AATAAATAAATAAAT | 83860 |
rs367697714 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929506 | GGCTTCAAGTGATCT[G/T]CCTGTCTCAGCCTCC | 83860 |
rs367722402 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881239 | ATGAGACCCTGTCTC[-/A]AAAAAAAAAAAACAA | 83860 |
rs367729117 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981507 | ATGCCTTTCAGAGAA[C/T]AATATTATTATCAAT | 83860 |
rs367766922 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976926 | GGTAATTATTTAAAT[G/T]CTCCACCAGAAATGA | 83860 |
rs367774531 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996898 | GAGGTTTCCCTATGT[C/T]GCCCAGGCTGGTGTC | 83860 |
rs367799542 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7932370 | TGGCATCTCAACTAG[C/G]TAGTGTTCCAGCAGA | 83860 |
rs367804730 | in-del | -/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998242 | AATCTGAGTGAGAAC[-/TA]TATATATATATATAT | 83860 |
rs367833091 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870553 | GATTTCCATTGTACA[A/G]TTGGAAACTGTAACT | 83860 |
rs367837533 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7948195 | AGCCTCCCGAGTAGC[G/T]GGGTCCACAGGTGGG | 83860 |
rs367839414 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842883 | GTTCCTGAAAAATCT[C/T]AGCACTGAATGTAAT | 83860 |
rs367840720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7928803 | AGCTTTTGTTTTCAG[A/G]TTCAGAGAGCTATAT | 83860 |
rs367858522 | snp | A/G | 1.7403e-05 | 0.00294978 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964527 | TGTGAGACCTGAAAC[A/G]CCCAACAGGACTCCT | 83860 |
rs367858877 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001611 | AGCATTTCCCTTTAT[G/T]GTTTCAGCTTTTGGT | 83860 |
rs367860723 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886093 | ACCACCATGTCTGGC[G/T]AATTGTTTTTTGTAG | 83860 |
rs367877886 | snp | C/T | 0.000509424 | 0.0159516 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009159 | CCCACCGCCGGCCCC[C/T]GCGCCCGCCCCCGGC | 83860 |
rs367879499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958954 | CCTGGCTAACATGGT[A/G]AAACCCCGTCTCTAC | 83860 |
rs367879646 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7949136 | GGGCTCAGCATTATT[A/G]TGTGAGTGTCTGTGC | 83860 |
rs367890858 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902514 | GTTGTTTTCTCATGA[C/T]GAAACTCAGGGGAAA | 83860 |
rs367900815 | in-del | -/AG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925814 | AAAAAAAAAAAAAGA[-/AG]AAAGAAAAGAAAAGA | 83860 |
rs367931790 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7907059 | ACAGTGTTCGTAGGG[C/T]CACCTGGCTTAGCTT | 83860 |
rs368003616 | snp | A/C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818144 | TTAGCTGAGGCAACA[A/C/T]CAGCGCAGGTCTGCG | 83860 |
rs368018551 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | TAF3 | GRCh38.p7 | 10:7975069 | GAACAAGACTCTGTC[A/T]CAAAAAAAAAAAAAA | 83860 |
rs368024460 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7860976 | GCTAATTTTTTTTTT[G/T]TGTGAGACGGAGTCT | 83860 |
rs368034928 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845503 | AATGATTTGGTTTGG[C/G]TGGTTCTGTTAGTCA | 83860 |
rs368049688 | in-del | -/CCCCC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967339 | GTGGAGTTGTTTCAA[-/CCCCC]CAGCCATTATGAATT | 83860 |
rs368050175 | snp | A/C/T | 1.66402e-05 | 0.00288441 | missense | TAF3 | GRCh38.p7 | 10:7965449 | GGCAGAGAAGATAAG[A/C/T]TGAAAGCCCCAGCAC | 83860 |
rs368058023 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827556 | GGAGGCGGAGACGGG[C/T]GGATCACGAGGTCAG | 83860 |
rs368059857 | snp | C/T | 2.03901e-05 | 0.0031929 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8014646 | GTGCAGGCCCTGTGT[C/T]GGAATCATGACTGCA | 83860 |
rs368062303 | snp | G/T | 1.86538e-05 | 0.00305394 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818661 | AAGGTCTGGCGGCGG[G/T]GCTGGAGAGCAGTGG | 83860 |
rs368121309 | snp | C/G | 1.65608e-05 | 0.00287752 | missense | TAF3 | GRCh38.p7 | 10:7824423 | ACATTGAGCCTGTCA[C/G]CTTCCCACACCAAAT | 83860 |
rs368181811 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818353 | ACCTGCCGCCCTGGG[C/G]GCCTCCTCCACCTGC | 83860 |
rs368197109 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856157 | GTCGAGAACTAGAAA[A/T]TAAAGGTAAGGAAAT | 83860 |
rs368216322 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829870 | TTAGGAACTCTTCTG[C/T]ATGGGGATTTCTCTC | 83860 |
rs368221839 | in-del | -/ACGTATAAAGACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936754 | CATGGGTTTGGACAA[-/ACGTATAAAGACA]TGTATCTACCATTGC | 83860 |
rs368245940 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986293 | CAGACTAATCTGCCA[A/G]GTTACTGGAAAGTTC | 83860 |
rs368262738 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949920 | CCTGTCCAATAAAGA[C/T]AGGAAGATACTACTG | 83860 |
rs368269711 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7910603 | CCAGGCTGGTCTCCA[A/G]CTCCTGACCTCAAAT | 83860 |
rs368329849 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992169 | TCATAGTAAAAGCAC[C/T]CTCTTGTTTGCTGCA | 83860 |
rs368332541 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014093 | TTAAAAATAATAATA[C/T]TAAAAGGAGATCCAG | 83860 |
rs368348330 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935789 | TCCAGGCCTTGAGGC[C/T]GAAGACTTCTCATTG | 83860 |
rs368351353 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969817 | CATGGCTTTGGCAGC[C/T]ACACTGACCGGGGTG | 83860 |
rs368355881 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954419 | TAGTTCTAGTTAACA[C/T]GAGCTCTCCATAGTG | 83860 |
rs368356365 | in-del | -/ACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974134 | TTCCTTCTGAAACAT[-/ACACAC]ACACACACACACACA | 83860 |
rs368358690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7925012 | TCTAGATTTGTAAGG[C/T]TCAAACTATATAAAT | 83860 |
rs368367776 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941029 | TGGAAAGCTCATGAC[-/C]TGTTGAAGTGGTGCA | 83860 |
rs368391306 | snp | C/T | 0.00174412 | 0.0294791 | intron-variant | TAF3 | GRCh38.p7 | 10:8009347 | TGCGTACCTGCCGCC[C/T]GCGCGGTTAGCATGG | 83860 |
rs368429464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981983 | TAGTAGTGAAGAATA[A/G]TCATGGGCAGTTACA | 83860 |
rs368439719 | snp | G/T | 0.000100371 | 0.00708347 | missense | TAF3 | GRCh38.p7 | 10:7965362 | AAAGAGAAGCATAAA[G/T]ATAAGAAGAAAGATA | 83860 |
rs368511709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7961825 | TCACTACATTTATCA[C/T]TCACCAAGGCTCAAA | 83860 |
rs368514440 | in-del | -/ACAC | 0.0178098 | 0.0926698 | intron-variant | TAF3 | GRCh38.p7 | 10:7881491 | CACACATACACACAA[-/ACAC]ACACACACACACACA | 83860 |
rs368530319 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010701 | CACTTGAGGTCAGGA[G/T]TTCGAGACCAGCCTG | 83860 |
rs368540914 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928980 | CCCTACTGTTAGAAC[C/T]GGAGTCTTGAAGAGA | 83860 |
rs368543659 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936094 | AAACAGAGAGAAGAC[C/G]TGACTCTAACCACAG | 83860 |
rs368549752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914037 | CATCAACCAATTGCA[A/G]TGTGGTCCTCTTTTA | 83860 |
rs368559545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7846172 | CCGTGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG | 83860 |
rs368560678 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996842 | GCACCACCACACTCT[A/T]TTTTTTTTTTTTTTT | 83860 |
rs368564600 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832915 | GTTATTTTTAAATGT[A/G]CAGGGTGCAGTAGCT | 83860 |
rs368574100 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828690 | CTAGATCACTGGTCA[A/G]TGGGGGTCTTCTGGG | 83860 |
rs368596361 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7930017 | GACCAGCCTGGGCAC[A/G]ATAGGGAGGCCCTGA | 83860 |
rs368623470 | snp | C/G/T | 5.39273e-05 | 0.00519237 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014766 | ACGACTCCCGAGGGG[C/G/T]TGGACCAAGCGGGGT | 83860 |
rs368647092 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894937 | CTGGAGTGCAGTGGC[A/G]TGGTCTTGGCTCACC | 83860 |
rs368656535 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014239 | TTATCTGTTTTTTAG[A/G]CCTCTTCAGCGGTTC | 83860 |
rs368686311 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896303 | CGTAGACCAAAACCA[-/A]TTCTTGCCAGAACCG | 83860 |
rs368690036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7992742 | TCATTCTGGATTGAA[C/T]GCATATTACCAACTT | 83860 |
rs368704120 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954901 | AGTTAACACAGAGCT[C/T]TCCATAGTGAGATTC | 83860 |
rs368707638 | snp | G/T | | | upstream-variant-2KB, missense | TAF3, LOC105376392 | GRCh38.p7 | 10:7818489 | GGCTTATGCTGCCTC[G/T]CCCCGGCGGCCGTCC | 83860 |
rs368742895 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996832 | CTACAGGCACGCACC[A/C]CCACACTCTATTTTT | 83860 |
rs368752994 | in-del | -/GC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856881 | AAAAAAAAAAAAAAA[-/GC]AGAAAGAATGCTTCA | 83860 |
rs368831185 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828978 | GAGGTTGCAGTCAGC[C/T]GAGATCGTGCCACTG | 83860 |
rs368856983 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863722 | ACATATATATATACA[C/T]ATATATATATACACA | 83860 |
rs368889597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972286 | TGGAAACAAAAATCC[A/G]GGAAGAAATTTTAAT | 83860 |
rs368913716 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944138 | GTGTGTGTGTGTGTT[G/T]TGGGGGGGAGGGAAA | 83860 |
rs368935581 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855012 | AGGGGTTTTAAGGTG[G/T]TGTTGTAGTTGTTAA | 83860 |
rs368946898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963515 | TCCTTGAAAACTAAC[C/T]TACTTTTTAAACACT | 83860 |
rs368969559 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011901 | AAAGCTTACTGGCTG[G/T]GCATGGTGTCTCACG | 83860 |
rs368980284 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008085 | CTGCAGCCCGTCTGG[-/G]AACAATCTTTTTTTT | 83860 |
rs368982164 | in-del | -/TTTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826456 | TTTTTTTTGTTTTGT[-/TTTGT]GTTGTTTTGATACTG | 83860 |
rs368987308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7867790 | GAGTTGGGGGCACAG[A/G]CCCCTGTGCAGAAAT | 83860 |
rs369023900 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851454 | AGGCCTTGTGGCAGG[A/G]GTTTGACTTTTACTC | 83860 |
rs369036053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7871737 | GCGGGAGCCACCGCG[C/T]CAGGCCAACGATTGC | 83860 |
rs369038346 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010506 | TTTCTGAATAATAGC[A/G]CTAATTATATTTTAT | 83860 |
rs369045147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7857504 | TGCCACACAGTCTTC[A/G]GAGTGTGGAGGTGGA | 83860 |
rs369071461 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982843 | ATAGGTGACCCAAAG[A/G]CATTTTTTGTTGACT | 83860 |
rs369073441 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917788 | GGGAATGAAGAAGGA[A/C]ATACTTTTGAAGTTA | 83860 |
rs369080982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886962 | TTAAGAGGGCCAGGC[A/C]CGGTGGCTTACACCT | 83860 |
rs369098036 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934634 | ATTTTTAGTAGGGAC[A/G]GAGTTTCACCGTGTT | 83860 |
rs369098155 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904870 | GCTGGCTGTGCTCCC[A/T]TTAGGCTGCACACAT | 83860 |
rs369104059 | in-del | -/AC | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7991404 | TTGCAGTATGGAAAA[-/AC]ACATTATTTTATTTC | 83860 |
rs369105929 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837129 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAAATTGC | 83860 |
rs369108412 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887590 | GACTTTCCTAGTGAT[A/G]AGTGTGAACTGTTTA | 83860 |
rs369126142 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835900 | ATGTTGGGAAGATGC[A/G]CAAACTACCTTGCCC | 83860 |
rs369133801 | in-del | -/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998266 | ATATATATATATATG[-/TA]TATATATATATATAT | 83860 |
rs369208444 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984405 | CTTACTTGTAAACAA[C/T]TACAGCAGTTCTTAC | 83860 |
rs369220057 | snp | A/T | 6.66367e-05 | 0.00577182 | intron-variant | TAF3 | GRCh38.p7 | 10:8013684 | GCCTCTTTTTGTTTT[A/T]TTTCCCATTCCCTCC | 83860 |
rs369230881 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880467 | ATCCTGACTAGCACC[C/G]TGAGAAAACAGTGTG | 83860 |
rs369301559 | snp | C/G | 4.97451e-05 | 0.00498699 | missense | TAF3 | GRCh38.p7 | 10:7964220 | ATGTACAGGACAGTA[C/G]AGACTTGGCACCTCC | 83860 |
rs369303084 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846243 | ATTACAGGCATGAGC[C/T]ACTGCGCCCGGCCAA | 83860 |
rs369357810 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863476 | TTAGCTGGGTGTGGT[A/G]GTGCACACCTGTTAT | 83860 |
rs369377030 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7951699 | TACAGTCTGACTCGT[A/G]CTTCTCATACTAAGT | 83860 |
rs369419155 | snp | A/G | 4.98658e-05 | 0.00499304 | missense | TAF3 | GRCh38.p7 | 10:7964684 | ATTGAGGCCTCTATC[A/G]ATGCTGTGATTGCAC | 83860 |
rs369429895 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957341 | ACATCACCCACAGAT[A/T]CTAACTCTGGATGTG | 83860 |
rs369441038 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825368 | ACATAAATGGACCAT[A/T]GTAAAGGTGTGCAGT | 83860 |
rs369469064 | in-del | -/GCTGCTCCGTTTT | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7865855 | TTTCTGCTCCTTCTA[-/GCTGCTCCGTTTT]ATGTCTCTTGCATCT | 83860 |
rs369490419 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011206 | TGGCTGGGTAGGACT[C/T]ATGGTATTTGTTGTT | 83860 |
rs369548677 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860804 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTGA | 83860 |
rs369554201 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959935 | CCTTTCTAGGGAATG[C/T]TTGGAGTAGAGCAGT | 83860 |
rs369557746 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926451 | AAAAAGTATTACCAG[A/G]TCCATATAGTATAAA | 83860 |
rs369568267 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831352 | GATTTCATTCATTAC[-/T]TTTTTTTTTTTGAGA | 83860 |
rs369575193 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972958 | TAAGCCATCAATATT[A/G]CCAGAAAAAGGACTC | 83860 |
rs369587477 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994281 | ATTCTTGTGTATTTC[C/T]ACAGATCTGGAATTA | 83860 |
rs369595842 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988409 | AGCCTGGCCAACATG[A/G]TGAAACCCTGTTTCT | 83860 |
rs369599137 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873560 | AACAAAATGTCATTT[A/T]CTAAATCTAAGTTTC | 83860 |
rs369626733 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7966889 | TGAAATGGGAATTCT[A/G]ATATCAATAACTGAA | 83860 |
rs369643659 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925823 | AAAAAGAAAAGAAAA[A/G]AAAAGAAAAAGGAAG | 83860 |
rs369656952 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014086 | CTTCTTATTAAAAAT[-/AA]TAATACTAAAAGGAG | 83860 |
rs369672829 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923659 | CCTGTATTCAATAGA[G/T]TAGCGGATACCTGAT | 83860 |
rs369714270 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840302 | TGACTACAGGCGCCC[A/G]CCACCACGCCTGGCT | 83860 |
rs369744653 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941641 | TGCGCCGATGCCTTC[A/G]AGGCTGTGAAATCCT | 83860 |
rs369752961 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962971 | AGGGCAAGTAACATC[A/G]GCTCCTTTTTGAAAG | 83860 |
rs369758098 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937779 | GTCAGGCCCTGTGCT[C/T]AGCACTCTTACATGC | 83860 |
rs369761740 | in-del | -/TGTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858806 | GTACATTATAGGCTC[-/TGTG]TGTGTGTGTGTGTGT | 83860 |
rs369767389 | in-del | -/ACTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910756 | GATGTTAACCTGGCT[-/ACTA]ACTAAAAGACAGGAA | 83860 |
rs369773645 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7892822 | CTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTGAG | 83860 |
rs369785707 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877597 | AATATTGCTTTGATA[C/T]AATGAATAATATAAA | 83860 |
rs369796173 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854650 | GAACTGAAAAGAGCC[C/T]TCTAATGGGGGGGCG | 83860 |
rs369801002 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7946027 | TTATGCACACCTGAC[C/G]CTGACTGTCCTCCTG | 83860 |
rs369856153 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858498 | TTTTTTCACTAGTTC[C/T]GGATCTTACTGATTA | 83860 |
rs369870838 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877004 | TCCTTTACTCAAATT[A/G]CCCACTTTCCTATCT | 83860 |
rs369898983 | snp | A/C | 1.66125e-05 | 0.00288201 | missense | TAF3 | GRCh38.p7 | 10:7964285 | AAATCACAAATGCCA[A/C]CTGCAAAACCATTAG | 83860 |
rs369905405 | in-del | -/TTTC | 0.31503 | 0.241394 | intron-variant | TAF3 | GRCh38.p7 | 10:7860781 | AGCTAACAGGAGCCT[-/TTTC]TTTCTTTCTTTCTTT | 83860 |
rs369917920 | snp | C/T | 0.000163987 | 0.00905353 | missense | TAF3 | GRCh38.p7 | 10:7964868 | CCACTCCTCTGCCTC[C/T]TTCCGGTGGAACCTC | 83860 |
rs369953396 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927974 | TTTTTGCTCCCCCAC[A/T]TTTTTTTTTGGAGTT | 83860 |
rs369986343 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867314 | AAAGATGTGATTTTT[A/T]AGTATGCATTTTAAA | 83860 |
rs370012080 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014037 | CTATTGTTATTCACC[C/T]TAAATTCTGAATATT | 83860 |
rs370021397 | in-del | -/ACAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863671 | CATATATATATACAC[-/ACAT]ATATATATATACACA | 83860 |
rs370043528 | snp | A/G | 1.68869e-05 | 0.00290571 | missense | TAF3 | GRCh38.p7 | 10:7965068 | CTGCCTTCCTCCGTG[A/G]AGGTAAAGAAGAAGT | 83860 |
rs370068673 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983844 | ACCCTGTCTCTAAAA[A/C]AATAAATAAATAAAT | 83860 |
rs370090816 | snp | A/G | 1.65781e-05 | 0.00287902 | intron-variant | TAF3 | GRCh38.p7 | 10:8013715 | ATTTTTGCCGCTTCC[A/G]CTTTGCAAACATCAG | 83860 |
rs370133494 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946728 | ACCCTGGTCTCAAAC[A/G]AAAAAAAAAGAAGGA | 83860 |
rs370155170 | snp | C/T | 3.3845e-05 | 0.00411355 | missense | TAF3 | GRCh38.p7 | 10:8009281 | CCTCCGGGGCCAGTG[C/T]CAAAGCCCCCGTGCG | 83860 |
rs370164376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7840189 | ACGGAGTCTCACACT[A/G]TCACCCGGGCTGGAG | 83860 |
rs370183247 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7922355 | ATGAGTTAGAAACTT[G/T]TGGGACTTTTCCATT | 83860 |
rs370187278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995091 | AGTAATAGTACCACT[A/G]TCACTACTACCACCA | 83860 |
rs370190011 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847431 | AAATTTACCTGACAC[A/G]AAAGGTTACATGTGT | 83860 |
rs370201694 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012508 | AGAGTCACGGCCTTC[A/T]GACTTCAAGCAAGGT | 83860 |
rs370210542 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821547 | TCTCAAGTTAAAGCA[A/C]GTATTAGAAGTTACC | 83860 |
rs370226181 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994843 | AGCTGGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 83860 |
rs370232255 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956461 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG | 83860 |
rs370236477 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953914 | AGAGTGCACTCCATA[G/T]GTGAATGAGCGGATT | 83860 |
rs370242363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7899285 | TCCCTTCCCCAGATG[C/T]CTTCTGCCCAAGGGA | 83860 |
rs370259163 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919906 | ATTGTTAGTCCCCCT[C/T]ATATTCTGTAATGAG | 83860 |
rs370262647 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877991 | CTTTGAGTAGACGCG[G/T]ACTTTGCAACTTGGC | 83860 |
rs370308170 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828920 | CTGTAGTCCCAGCTA[C/G]TCGGGAGGCTGAGAT | 83860 |
rs370370175 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7862855 | AATTCTGGATATTTT[A/G]CAAATATCCATAAGT | 83860 |
rs370373369 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861797 | TTCTTTCTTTTTTTT[-/T]CTCAATGCTTGGGAG | 83860 |
rs370409156 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009446 | AAATTTTATTATTTA[C/T]TTAATTATTTTTGAG | 83860 |
rs370414931 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836820 | ATCCTCTAAACGAAA[C/T]TATTAGACAAAAAAT | 83860 |
rs370433147 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868319 | AGTGGTCCAGCTCTG[A/G]TGATTCAGGAGTGGA | 83860 |
rs370448272 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935149 | GTGCGTGCTGGTGCG[C/T]GCCTGTAATCCCAGC | 83860 |
rs370450539 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917308 | GCATTGAAGCAAATC[A/G]AAGGGAAGAAGTCCA | 83860 |
rs370474332 | snp | A/G | 5.04503e-05 | 0.00502221 | intron-variant | TAF3 | GRCh38.p7 | 10:7977237 | AATGTGCTAACTTCC[A/G]CAGATAAAAGTGGAA | 83860 |
rs370476884 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875043 | AGATAGCAGTTTGTA[C/G]GTTTTCCTTGTTTTA | 83860 |
rs370542451 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922672 | GTAAACAGATGGCTG[A/G]CAATCCCTTGATCAT | 83860 |
rs370574432 | snp | A/G | 4.985e-05 | 0.00499225 | intron-variant | TAF3 | GRCh38.p7 | 10:8013888 | TAGGCAGCATCAGCC[A/G]CTCCTGAGATGAAGC | 83860 |
rs370617634 | in-del | -/AAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963217 | CCTGATAATAATAAT[-/AAT]CCATACTAAGTCCTA | 83860 |
rs370646387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942748 | CGAGGCGTGTGGGCA[C/T]GGAGTTCTAGATCTT | 83860 |
rs370650612 | in-del | -/T/TT/TTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844378 | TTCTTCTTCTTGTTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 83860 |
rs370660427 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838929 | TTTTTTTTTTGGTTT[G/T]TTTGTTTTGTTTTGT | 83860 |
rs370661066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821882 | TGTATAAAGGTATAG[A/C]GTATTCCAGCTTAGA | 83860 |
rs370707519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7881574 | TAATAAGTTTTTTAT[A/G]TCAAATAGGTATATG | 83860 |
rs370709866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865411 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 83860 |
rs370732059 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961437 | TTGGCCTCATCCTCG[C/T]TGACCTCTTAAGCAT | 83860 |
rs370739825 | snp | C/T | 6.65303e-05 | 0.00576721 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964917 | GACAATGGATGCCTC[C/T]ATTGATGAGGTTGTA | 83860 |
rs370768126 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905610 | AGCAGGGCCAGGCGC[A/G]GTGGCTCACACCTGT | 83860 |
rs370779007 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874406 | GTTATATATATCTTA[C/T]CCCTGGGCTTTCCTG | 83860 |
rs370795997 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954178 | GAGATTCAGAGTGCA[C/T]TCCATATATGAATGA | 83860 |
rs370806207 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935474 | CTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 83860 |
rs370817870 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7906882 | ACCACCATGCCCAGC[A/G]TACACCTTATTCTTC | 83860 |
rs370856885 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845327 | GTGTGCGTGTGTGTG[-/TG]CACACGGTTCCTGCT | 83860 |
rs370882550 | snp | C/T | 1.79451e-05 | 0.00299537 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009087 | TGACAGTGTCATCAG[C/T]AAGGTGGTCCCTGCC | 83860 |
rs370924681 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | TAF3 | GRCh38.p7 | 10:7927441 | AGGCTTGAAAATGTG[C/G]AAGAGAATTTCCCAG | 83860 |
rs370990536 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015234 | TCCAGTTGGAGTACC[A/G]GTAAATATTTTTGTG | 83860 |
rs371012035 | snp | G/T | 0.000167986 | 0.00916323 | missense | TAF3 | GRCh38.p7 | 10:7964392 | CCAGTCACCAGCAAT[G/T]GTCGGAAGTCCTATT | 83860 |
rs371068019 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860804 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTGA | 83860 |
rs371077188 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011922 | GTGTCTCACGCCTAT[A/C]ATCCCAGCACTTTGG | 83860 |
rs371100096 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970565 | AATGCAAATGAGGGG[A/G/T]ATAGGAATGGTTTGA | 83860 |
rs371127555 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995002 | AAAAAAAAAGAAAAA[A/G]GAAATCCTGAGTCTT | 83860 |
rs371133957 | snp | A/C | | | missense | TAF3 | GRCh38.p7 | 10:7965465 | TGAAAGCCCCAGCAC[A/C]CCCACTGGTGTTGCC | 83860 |
rs371142607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7887835 | AAAAAAAAAAACACC[A/G]AAACAAATTATAGAA | 83860 |
rs371148222 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931856 | TCAAAGTATTGTTTT[G/T]TTGTCTTTGGCCTCA | 83860 |
rs371152433 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947671 | GAGTTTGAGAAGCAT[C/T]GAAGATGCCAGCATG | 83860 |
rs371155531 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915420 | GAGGCCGAGACGGGT[A/G]GATCACGAGGTCAGG | 83860 |
rs371174417 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858887 | GTGCATATGAACATG[G/T]GAATGTATCCTCCTC | 83860 |
rs371190996 | snp | C/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016959 | AATGGAATACAGAGC[C/G]TTTCACCTCTAGGTC | 83860 |
rs371203936 | in-del | -/CTGGTCCCTCGAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848554 | TCCAGGTCCCTCGAC[-/CTGGTCCCTCGAC]AGCTGCTAGATATCC | 83860 |
rs371213199 | snp | A/G | 0.000293015 | 0.0121005 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965196 | TAAAGTGAAAGAGAA[A/G]GAGAAAGACAAGGAA | 83860 |
rs371220200 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996945 | ACAGTCTGCCTGCCT[C/G]AGCCTCCCAAAGTGC | 83860 |
rs371224103 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849110 | TGTTTCCTTAGGTAC[C/G]AAGTGCTTCACACAC | 83860 |
rs371242459 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925766 | ATTGTGCCACTGCAC[A/T]CCAGCCTGGGCAACA | 83860 |
rs371243199 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877320 | TGGTGGTATGGAAAT[A/C]TGGGAGGTTTTTCTT | 83860 |
rs371259718 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948303 | CTTGTTGCCCAGGCT[C/G]GTCTTGAACTCCCAG | 83860 |
rs371272934 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997299 | TTAGGAACTTTGTGT[G/T]CAGTTTAGTAGCCAG | 83860 |
rs371282048 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008287 | ATTTTTTAGTAGAGA[C/T]GGTGTTTCACCATGT | 83860 |
rs371296400 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967407 | CCATGCCTTTCTACA[A/G]CATCTACCTGACTTT | 83860 |
rs371297760 | snp | C/T | 0.00028173 | 0.0118653 | intron-variant | TAF3 | GRCh38.p7 | 10:8013860 | CCCAGGGCGCCCTGC[C/T]GGCCACACTCATTAG | 83860 |
rs371297884 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999029 | AATGACTAGGTGGCT[G/T]AGGAAGTGGAATCTG | 83860 |
rs371301707 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7965990 | ATCACAGACTATAAA[A/C]TCTCTATTAGCTATA | 83860 |
rs371337127 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879194 | TTAATAAGACATTTA[G/T]ATGTTCTATTTGCCC | 83860 |
rs371371063 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820643 | GGGACTACAGGGATA[C/T]GCCACCATGCCTGGC | 83860 |
rs371416699 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922317 | TTCTTTATTGCTGTT[C/T]CATAGAATCAGAGGA | 83860 |
rs371440621 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7998511 | TTAAGCCATTCTAAT[-/G]GGCGCCATTATCAGG | 83860 |
rs371468674 | snp | A/C | 1.66888e-05 | 0.00288862 | missense | TAF3 | GRCh38.p7 | 10:7965501 | AAGAGTTGGCCCTGC[A/C]CTTGTTCAGCCCTGC | 83860 |
rs371526886 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954917 | CCATAGTGAGATTCA[-/A]GAGTGCACTCCATAG | 83860 |
rs371562719 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925828 | GAAAAGAAAAGAAAA[A/G]AAAAAGGAAGGAAGG | 83860 |
rs371611766 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996381 | TATGACCTATCCTTG[A/G]AGGTGACGTGGTTAT | 83860 |
rs371620029 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957206 | CCAGAACTACCTTTC[C/T]TTAGTTAAATACCCA | 83860 |
rs371658927 | snp | A/G | 6.63152e-05 | 0.00575788 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964137 | CTTGGCACCTCCCT[A/G] | 83860 |
rs371671822 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827304 | CACCTACCACATTGG[A/G]GAAATGGAGAATCAA | 83860 |
rs371698155 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959734 | CCTCACATTCTTCCT[C/T]CATTCAAAGGCCTAT | 83860 |
rs371706285 | snp | C/T | 3.31214e-05 | 0.00406935 | missense | TAF3 | GRCh38.p7 | 10:7824441 | TCCCACACCAAATTC[C/T]GTCATTTCCTGTTAG | 83860 |
rs371709049 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972475 | CAATCCCAGTTATGT[A/G]GTATAATTAATAGCT | 83860 |
rs371724490 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896779 | ACTGAGTTATTTTCA[A/G]CAGTTTCTGTAGGAC | 83860 |
rs371728674 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955571 | GTCAGATAAAAAGCT[C/T]CTATGCCATGTGCAA | 83860 |
rs371732698 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922833 | GGAGTTCATTTTATC[C/T]CAGCCTTATCACTTT | 83860 |
rs371732848 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003106 | ATACAGCCTGACAAC[G/T]GAATCACTTAGACCT | 83860 |
rs371797522 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861499 | GATGGGACAAGTCAG[A/G]TTCATCTTGTATATG | 83860 |
rs371810929 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981682 | TGATTTCTGGTGGCA[A/G]GTGGATTGATTTCTT | 83860 |
rs371837388 | snp | C/T | 1.66283e-05 | 0.00288338 | missense | TAF3 | GRCh38.p7 | 10:7964720 | TGTGCTGAGCGAGAG[C/T]CAGATCCTTTCGAAT | 83860 |
rs371837470 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7883275 | CATGACCTCACCACT[G/T]TGGAAGAGAACAAAC | 83860 |
rs371846010 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882298 | TTCCTCATTTACAAC[A/T]TGTTTGTGCAAGACA | 83860 |
rs371849639 | in-del | -/ACTTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999860 | TGGATGATGCACTCA[-/ACTTA]GACGCACTCGATTGT | 83860 |
rs371858693 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852855 | TATGAAAAGCTGGAT[A/G]AATGCTTGATCCCTT | 83860 |
rs371956537 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846044 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 83860 |
rs371977159 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7961968 | GACCCTTGCACCTCA[A/G]TCTCCCAGGTAGCTG | 83860 |
rs371985194 | in-del | -/GTCTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825593 | ACTTGGACATTATTT[-/GTCTTT]TTATGACTGGCTTAC | 83860 |
rs372023342 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896303 | CGTAGACCAAAACCA[A/G]TTCTTGCCAGAACCG | 83860 |
rs372087205 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:8006710 | AATTTATGATCAGAA[G/T]AGCAAAGAGTCAGTG | 83860 |
rs372092838 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914056 | GGTCCTCTTTTAGAT[A/C]CCGATTCAAAGAAAC | 83860 |
rs372103304 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935819 | GATTCAGGAGAAAAG[G/T]GCAACTGGACCTGAA | 83860 |
rs372104531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7977559 | TTTCTCTTTTTTAAA[A/G]ACTAGCACCTGACAT | 83860 |
rs372119567 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996827 | TGGGACTACAGGCAC[A/G]CACCACCACACTCTA | 83860 |
rs372165400 | snp | C/G | 8.66814e-05 | 0.00658279 | missense | TAF3 | GRCh38.p7 | 10:7964533 | ACCTGAAACGCCCAA[C/G]AGGACTCCTTCAGCT | 83860 |
rs372196675 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855927 | TTCTCCACAAAAAGG[-/A]AAAAAAAAAAAGACA | 83860 |
rs372196685 | snp | A/G | 0.000491879 | 0.0156748 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009162 | ACCGCCGGCCCCCGC[A/G]CCCGCCCCCGGCCCC | 83860 |
rs372205047 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987563 | ATTCAGTGTTACTAG[G/T]TCAAAGAATGTAAAC | 83860 |
rs372227205 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962375 | CCTCATCCATCCTGC[A/G]TGTTCCTGCCAGTGT | 83860 |
rs372236995 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935514 | GCGTGAACCCGGGAG[A/G]CGGAGCTTGCAGTGA | 83860 |
rs372278422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945161 | CTGGCCTCTGGCACC[C/T]GTGGCATTAGAGGAC | 83860 |
rs372298111 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899876 | AAAATACTAAGAAAA[G/T]GTAAACTGCAATATT | 83860 |
rs372298222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7835271 | AGAAAGTTTACAACT[C/T]TGTGTTGGGCTGCAT | 83860 |
rs372302098 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7914980 | GAGTCTTGCTCTGTC[A/G/T]CCCAGGCTGGAGTGC | 83860 |
rs372303875 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7848475 | ACAGGTAATACTCAA[G/T]TGCAGACAAAATCTT | 83860 |
rs372324720 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854328 | ATAGCAGCCCCCAAA[C/G]TGCCTACGTAAGATA | 83860 |
rs372335188 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969342 | TATCCAATTGCAGTC[A/C]CAGCCATAATAGTTG | 83860 |
rs372353141 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822398 | AGGAATAGAAGAGAT[G/T]AAATGCCTGTTTACA | 83860 |
rs372355248 | snp | A/C | 1.81312e-05 | 0.00301086 | missense | TAF3 | GRCh38.p7 | 10:7963923 | TTCCTTTACCAGAAG[A/C]AGAAGAAGAGCAGGT | 83860 |
rs372368199 | snp | G/T | 0.000165986 | 0.00910855 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014780 | GCTGGACCAAGCGGG[G/T]TCAGCCCGGGCTTCT | 83860 |
rs372368784 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827831 | GGGCATGGTGGTGCA[C/T]GCTTGTAGTCCCAGC | 83860 |
rs372377693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889956 | TTTCCTCCCTCCTCT[A/G]GTTTATCTTCCATCC | 83860 |
rs372421047 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933071 | TAGCCTACTGCCTTA[A/C]AAGAAGGGGGGATAA | 83860 |
rs372433356 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961436 | GTTGGCCTCATCCTC[A/G]TTGACCTCTTAAGCA | 83860 |
rs372436271 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901546 | GTATTATGTGTGGCT[-/G]GTTTAGATGGCCAGT | 83860 |
rs372450673 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871134 | TTTATTAGTTCACTT[A/G]AAAGTTTCCTATCAT | 83860 |
rs372454375 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856735 | AAAGTGACTTGGAAC[A/T]TTTTGTTATACCAAG | 83860 |
rs372458646 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7857647 | TTATTTCATGAAAGG[G/T]TAATTGTATTTTGAT | 83860 |
rs372467641 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843726 | TGTGCTTATGTCACA[C/T]ATACAATTAACATGC | 83860 |
rs372478014 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879724 | GCCATAGTTATTTAC[C/T]TTTCTGGATTTATGG | 83860 |
rs372519186 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7911150 | TAAAGAAGGTGCTTT[A/C]AGAAAAAAGTGGTGT | 83860 |
rs372566714 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816680 | TGAGGCTTTCTTGCC[A/G]AGGAATTCACTGCAC | 83860 |
rs372573148 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829290 | ACGTGACTATGGTAC[A/G]TGTATCACAATTAAT | 83860 |
rs372579354 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820802 | GCCCAGCTCACTGAT[A/G]CATCTGAATGTGGAA | 83860 |
rs372613300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7843399 | CAGGCATGAGCCACC[A/G]TTCCCAGCTTACAGT | 83860 |
rs372724074 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840213 | GCTGGAGTGCAGTGG[C/T]GCCATCTCGGCTCAC | 83860 |
rs372745612 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996859 | TTTTTTTTTTTTTTT[G/T]TATTTTTGTATTTTT | 83860 |
rs372752198 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993833 | AAGGTGAACCTCAGC[A/G]ACCCTGAAATACACC | 83860 |
rs372766346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010691 | GCAGATGGATCACTT[A/G]AGGTCAGGAGTTCGA | 83860 |
rs372780512 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970909 | TCATTCCAAGTCTTT[G/T]CTCATCAGCTATTGT | 83860 |
rs372783506 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010877 | CGTACCACTGCTCTC[C/T]AGCCTGAGGGACAAG | 83860 |
rs372817827 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999946 | ACTAGACTATGGTCA[A/G]CATTTGCCTGGAAGG | 83860 |
rs372839774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7934873 | GAGCCCCTCCCATGC[A/G]GCAGGCATGTTCTAG | 83860 |
rs372841177 | in-del | -/ACACAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863689 | TATATATATATACAC[-/ACACAT]ATATATATATACACA | 83860 |
rs372845704 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927677 | AAAAATCACTTATAA[C/T]CCCTTCCTCCTTAAA | 83860 |
rs372894932 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933668 | CATGCACATATACAC[A/T]TCAGTGCTGTCTTTC | 83860 |
rs372896643 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900504 | AGCTATCCAACCACT[A/G]TTGTGTGGTCCTGAA | 83860 |
rs372902098 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999458 | AAAGAAAGAAAGAAG[-/T]TTTTTTTTTTTTTTT | 83860 |
rs372920722 | snp | A/G | 0.000167986 | 0.00916323 | intron-variant | TAF3 | GRCh38.p7 | 10:8013691 | TTTGTTTTTTTTCCC[A/G]TTCCCTCCATTTTTG | 83860 |
rs372928890 | in-del | -/T/TT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7949766 | ATAAAACATTTTTTT[-/T/TT]AACTGCATAGACCAA | 83860 |
rs372938978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7947285 | CCTCCAGCCCCCACC[A/G]CAGGCCGGATAGTGC | 83860 |
rs372956628 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941008 | AAACAATATAAAATA[-/C]AGAAGTGGAAAGCTC | 83860 |
rs372959114 | snp | C/T | 1.65963e-05 | 0.0028806 | missense | TAF3 | GRCh38.p7 | 10:7964247 | CTCCCTCACCCGAGC[C/T]GCCAATGTTGGCTCC | 83860 |
rs372962729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7841958 | CAGACTTGGTTGCTT[A/G]TGTTAAGGGCAGCAG | 83860 |
rs372963030 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915310 | TGCTGCCGGAGGGGC[A/G]AAGTCTCACTTACAG | 83860 |
rs372978264 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897512 | CTGTGATTTGCCTTC[A/T]TGCGTGTTTTGTTTT | 83860 |
rs373006983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837879 | GTTTATTCTTACAAC[A/G]TAGATTACTTACTGA | 83860 |
rs373012239 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994456 | AAAAGAAAAGAAAAA[A/G]AACTATGAGTTTATA | 83860 |
rs373012426 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915411 | GCACTTTGGGAGGCC[A/G]AGACGGGTGGATCAC | 83860 |
rs373020523 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901920 | AAATTTGATAATCTT[A/T]TCATTTTGCCACATT | 83860 |
rs373029769 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885575 | CAGTCTCATTAGTTT[C/T]TGCTTTATCCTTCCT | 83860 |
rs373073559 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915149 | GTTTCACCATGTTAG[C/T]CAGGATGGTCTCGAT | 83860 |
rs373092239 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884503 | GCGATTCTCCTGTCT[C/T]AGCCTCCCGAGTAGC | 83860 |
rs373099957 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944139 | TGTGTGTGTGTGTTG[G/T]GGGGGGGAGGGAAAA | 83860 |
rs373106036 | in-del | -/AAAAAAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944456 | TTAAGAGAAAGAAAT[-/AAAAAAT]GAAACGCAGTAAAAG | 83860 |
rs373123656 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8013808 | GAGTCCCATGATTGG[A/G]TGTGACGACTGCGAT | 83860 |
rs373125256 | in-del | -/CAAACAAA | 0.409721 | 0.192325 | intron-variant | TAF3 | GRCh38.p7 | 10:7865478 | AGTGAGACTCCGTCT[-/CAAACAAA]CAAACAAACAAACAA | 83860 |
rs373171508 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844407 | TTTTGAGACGGAGTC[G/T]TGCTCTGTCACCAGG | 83860 |
rs373176829 | snp | C/T | 3.36508e-05 | 0.00410174 | intron-variant | TAF3 | GRCh38.p7 | 10:7977236 | TAATGTGCTAACTTC[C/T]ACAGATAAAAGTGGA | 83860 |
rs373179493 | in-del | -/CT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873629 | TCTCCCCCCCCCCCC[-/CT]GTCAAAAGGGGGTGT | 83860 |
rs373235777 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892900 | TCTTGGCTCACTGCA[A/G]CCTCTGCCTTCTGGG | 83860 |
rs373240882 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877728 | CTGAGACCCATTGTG[A/G]TGAAGTGACTTGGCC | 83860 |
rs373273782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7846987 | CCTTCTTTTTAGTCT[A/G]CTTATAGCTTTCATT | 83860 |
rs373290750 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011903 | AGCTTACTGGCTGTG[C/G]ATGGTGTCTCACGCC | 83860 |
rs373302260 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871615 | GCCTGGCTAATTTTT[-/T]GTATTTTTAGTAGAG | 83860 |
rs373328543 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865498 | AAACAAACAAACAAA[C/G]AAACAAAGAAACAAA | 83860 |
rs373350330 | in-del | -/CTCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957792 | ACGCTCTCTCTAGCG[-/CTCT]CGCTCTCTCTCTCTC | 83860 |
rs373418866 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004856 | GTCTCAGGTACTCTT[C/T]GTTAACATTCGTCTC | 83860 |
rs373419519 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822262 | AAAAAAAAAAAAAGG[G/T]GGCCGAAGGGGACGG | 83860 |
rs373425677 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963570 | GAAATCATGTTTGAA[C/T]GCCGCATGTTCTCAC | 83860 |
rs373433243 | in-del | -/AACGTATAAAGAC | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7936753 | CCATGGGTTTGGACA[-/AACGTATAAAGAC]ATGTATCTACCATTG | 83860 |
rs373452004 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900679 | AACTATTTTTATAAA[A/C]ATTTTTATTTCTAAA | 83860 |
rs373500668 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968317 | ACACTGACCCAGATC[A/G]GCAAGCAAGAGCATT | 83860 |
rs373515827 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957789 | TCTCACGCTCTCTCT[A/C]GCGCGCTCTCTCTCT | 83860 |
rs373520326 | snp | C/G | 1.66045e-05 | 0.00288132 | missense | TAF3 | GRCh38.p7 | 10:7964871 | CTCCTCTGCCTCTTT[C/G]CGGTGGAACCTCAAG | 83860 |
rs373541840 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881558 | CAATGAAGCTGGAAC[A/G]TAATAAGTTTTTTAT | 83860 |
rs373559299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7892539 | AGCATATAGCATTTT[A/G]TATCTTTCAATATAT | 83860 |
rs373580012 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882566 | TAACCACAGGAAAAG[A/G]CACGTAGGTTTATTG | 83860 |
rs373633618 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829557 | TGGAATTTTTCTGAT[A/G]TTTTCCTCATGATTA | 83860 |
rs373679380 | in-del | -/AGTT | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7894127 | AAGCTCTCAGTTGAC[-/AGTT]AGCCATTCTAATGGA | 83860 |
rs373692942 | snp | C/T | 1.65941e-05 | 0.00288041 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824553 | ACCCATTGTGTCTTC[C/T]CAAGAAGGTTTGTGA | 83860 |
rs373732342 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872238 | TTTTTTTTTTTCTTT[C/T]TTTCCCAGTAGCTAC | 83860 |
rs373743227 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920300 | AAAATTTAAACATAC[-/GT]GTGTGTGTGTGTGTG | 83860 |
rs373770059 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7834866 | TTTCTTTCATTTTAC[C/T]GTGTGTATCTTGTCA | 83860 |
rs373796517 | snp | C/G | 6.99753e-05 | 0.00591462 | missense | TAF3 | GRCh38.p7 | 10:7965143 | AGAGATAGGGAGAGG[C/G]AAAAAGACAAGAACA | 83860 |
rs373808466 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927975 | TTTTGCTCCCCCACT[C/T]TTTTTTTTGGAGTTC | 83860 |
rs373851676 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014898 | AGGCTGGAACACACC[A/G]CGCACCTGGATTGTT | 83860 |
rs373865300 | in-del | -/TTTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996034 | ACTTCTGAATATTTA[-/TTTA]CATACCTAAGTTAGA | 83860 |
rs373931109 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983485 | GAACATTTCAGAACG[C/T]CATCCTGTCAGACTT | 83860 |
rs373975801 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875157 | GTCACTATTTATATG[A/G]TAGTAAATAATCACC | 83860 |
rs373986757 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998646 | GAGTTCGAGACCAGC[A/C]TGGCCAACATGGTGA | 83860 |
rs373999915 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934990 | ATTAATAAATACTAA[G/T]AAGAGGCTGGGCACA | 83860 |
rs374013108 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960077 | CATACTCTAAAGACC[C/T]GTTATCCTGCCTAAG | 83860 |
rs374019559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905652 | TGTGGAAAGCTGAGG[C/T]GGGCAGATTACGAGG | 83860 |
rs374028504 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917452 | TAGAGAGAATGGTGG[A/G]AGGTAACTGTGGAAC | 83860 |
rs374035758 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948611 | CCTAGTGTGTTGGGT[A/G]TTTTGACTCACCAAA | 83860 |
rs374053215 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | TAF3 | GRCh38.p7 | 10:7844995 | CTTATGATAAATTCC[C/G]AGGGTAGAAGTTTTT | 83860 |
rs374058116 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867270 | ACACACACACACACA[-/CA]AAAAACAAAAAACAA | 83860 |
rs374075122 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893100 | GCTGGGATTATAGGC[A/G]TGAGCCACCGTGCCC | 83860 |
rs374079684 | snp | A/G | 1.66721e-05 | 0.00288717 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964941 | GGTTGTACGTAAAGC[A/G]AAACTGGGAACACCT | 83860 |
rs374088587 | snp | C/T | 8.92857e-05 | 0.00668093 | intron-variant | TAF3 | GRCh38.p7 | 10:8014630 | CTGAGCTTGTTTTCA[C/T]GTGCAGGCCCTGTGT | 83860 |
rs374125903 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953924 | CCATAGGTGAATGAG[C/T]GGATTAGTCCTAGTT | 83860 |
rs374132658 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855326 | AAAAGACTGACTTCA[A/G]AGGGCCAAACAAAGG | 83860 |
rs374153806 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7911634 | AAGGAGGTGGGTTGT[G/T]GGACACAGTTTTCAT | 83860 |
rs374165377 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866764 | AAGCCCAATTAGAGG[C/T]GAGTGTTAGGAAAAC | 83860 |
rs374188002 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839504 | AAAATTAGCTTGTCC[A/G]AAGTCACATGGCTGC | 83860 |
rs374189521 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847892 | CCTGAGGCTGAGCCT[A/C]CCGAGTAGCTGAGAC | 83860 |
rs374197487 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855441 | GAATACACCGGATGC[C/T]GAGATGTCCAGCCTC | 83860 |
rs374218228 | in-del | -/GAAAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999439 | GTTAAAAAAAAAAAA[-/GAAAG]AAAGAAAGAAAGAAG | 83860 |
rs374242405 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816639 | AGGGCCACTCCAGCT[C/T]CTGCACACTATGGCA | 83860 |
rs374271445 | in-del | -/CAAACAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865498 | AAACAAACAAACAAA[-/CAAACAAA]GAAACAAACAGAAAG | 83860 |
rs374272292 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935520 | ACCCGGGAGGCGGAG[C/G]TTGCAGTGAGCCGAG | 83860 |
rs374274132 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985259 | TCTTACATCCCCCAC[A/G]GCTTGTCGTCCAGGC | 83860 |
rs374299192 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851640 | TGCCCCTTTCCCTTC[C/T]CCCCTTTCATGTTGG | 83860 |
rs374304831 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838039 | ATTTAATCTTGAAAC[A/G]GGTCCTAAAGGCAGA | 83860 |
rs374311387 | snp | C/T | 1.74293e-05 | 0.00295201 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964521 | AACACCTGTGAGACC[C/T]GAAACGCCCAACAGG | 83860 |
rs374325361 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973405 | TACCTCATCACTGAT[-/G]ACTGTGTAACCCTAA | 83860 |
rs374330193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000360 | AACCTCAGGTGATCC[A/G]CCTGTGTTGGCCTCC | 83860 |
rs374339793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7898524 | GCGCTCCAGATTGGG[C/T]GACAGAACAAGACTC | 83860 |
rs374346258 | snp | A/G | 0.000173599 | 0.00931501 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964491 | GAGCCCCAAGGTCAC[A/G]ACTCACATTCCCCAA | 83860 |
rs374351799 | snp | A/G | 0.00077636 | 0.019687 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014760 | CCACTGACGACTCCC[A/G]AGGGGCTGGACCAAG | 83860 |
rs374376981 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998439 | TCTGAGATTTTAACT[A/G]TTAACCCATAAAATT | 83860 |
rs374388109 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007084 | ATGGGGCTTGGAGAA[C/G]TCCTTGAACAGTTCT | 83860 |
rs374416549 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967338 | CAGTGGAGTTGTTTC[A/C]ACAGCCATTATGAAT | 83860 |
rs374425298 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988772 | AAAAAAAAAAAAAAA[A/T]CAAGATTATCAAGTA | 83860 |
rs374439130 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862764 | TTCTAGAATTTTATA[C/T]AAGTGAAATCATGGT | 83860 |
rs374443718 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940055 | AGAGATTAGGAGGAA[-/A]TTATATGTGCTTGCC | 83860 |
rs374446823 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924177 | ACTATTCTAAATGTG[G/T]TGCCAGGGTATTTGA | 83860 |
rs374465176 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945625 | CAGTAACTACCCACC[C/T]GGCTACATCCTGAGA | 83860 |
rs374485122 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878018 | TGGCATTTATTCAGT[A/C]AACATTTTTTTTAAG | 83860 |
rs374498418 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7965996 | GACTATAAACTCTCT[A/G]TTAGCTATAGTGATC | 83860 |
rs374505928 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983713 | ACGTAGTGGCGTGCA[C/T]CTATACTCCCAGCTA | 83860 |
rs374512870 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911935 | GGTTCCTAAAGGCAC[C/T]TAAGTTTAAAGCCCT | 83860 |
rs374525723 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996826 | CTGGGACTACAGGCA[C/T]GCACCACCACACTCT | 83860 |
rs374528713 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848797 | GGCATAAACTTTATG[C/T]CAATATGCCTTTATA | 83860 |
rs374578457 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902315 | GTAATCCCAACTACT[C/T]GGGAGGCTGAGGCAG | 83860 |
rs374580034 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961784 | TCATTGTCCTTTTCT[A/G]TTTCCTTATTTCCTG | 83860 |
rs374603046 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865443 | GAGATCGCGCCTCTG[C/T]ACTCCAGCCTGGGGG | 83860 |
rs374611755 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912770 | CATTGCCAGTGGCTT[A/G]ATCCGTCAGTCCAGG | 83860 |
rs374620708 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896590 | TTGGGGACAGATTTA[C/G]CTAAGTTGCAGTAAG | 83860 |
rs374628790 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934840 | CTAACTAATCTATTC[A/G]TTTCAAAAATATTCA | 83860 |
rs374648148 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890843 | TCTTTCCAAAGCTTT[C/T]GATTTAGGTTTCCTT | 83860 |
rs374651811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7876154 | TAAATTAATTTTGTG[C/T]GGTGTTTTATATTTT | 83860 |
rs374666794 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833391 | TCTTTTTTATAGCAG[C/T]CATTCTAACAGGTGT | 83860 |
rs374689874 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014090 | TTATTAAAAATAATA[A/T]TACTAAAAGGAGATC | 83860 |
rs374703026 | snp | C/T | 1.79316e-05 | 0.00299424 | intron-variant | TAF3 | GRCh38.p7 | 10:8009054 | TCCTGTTTTGACTTT[C/T]ACCTTCTCTTCTTTT | 83860 |
rs374708896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7888167 | AAAGTTTTTCCTGAA[C/T]GCTGTCTTCCTCTAG | 83860 |
rs374730752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889434 | ACTATTCACATCTGT[C/G]TGTTACAGATGAGGA | 83860 |
rs374781807 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996626 | TGACATTTCAATGTC[-/T]TTTTTTTTTTGTATT | 83860 |
rs374802424 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863579 | CGCCCCACTGCACTC[C/T]AGCCTGATGACCAGA | 83860 |
rs374811441 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7950232 | AATATGTCTTTGAAA[A/G]GACAGTATTACTCTT | 83860 |
rs374813824 | in-del | -/TCTGAAATCAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822229 | GAGAAAGGAAAAAAA[-/TCTGAAATCAT]GGTTAAAAAAAAAAA | 83860 |
rs374833674 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826562 | GAAACTCATTTAGTT[A/T]TATGCAAACAATATA | 83860 |
rs374853895 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009750 | CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG | 83860 |
rs374886161 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010780 | CTGGGCATGGTGGCA[C/T]GTGCCTGTAATCCCA | 83860 |
rs374911988 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TAF3 | GRCh38.p7 | 10:7878106 | CCTTCCTGTGTTATT[A/G]ATTCTAAAACATGAT | 83860 |
rs374928604 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847555 | GCTCAAGGGATCTTC[C/T]GCCTCAGCCTTCTGG | 83860 |
rs374952381 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016975 | TTTCACCTCTAGGTC[A/G]GTGAGTCGGATCCAG | 83860 |
rs374964094 | snp | C/T | 0.000718457 | 0.0189397 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7977258 | AAAAGTGGAACCAGT[C/T]GCTCTGGCCCCGAGT | 83860 |
rs374970057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958950 | CCATCCTGGCTAACA[C/T]GGTAAAACCCCGTCT | 83860 |
rs374979908 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918184 | AATGCGTAAAACAAG[A/C]AACAGTTAAGGACTG | 83860 |
rs374982582 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887556 | ATGAGAGAGCAGAGT[A/G]GATGAAAATGCAACA | 83860 |
rs374995246 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857806 | AAAAGGCAGGGGAAA[A/T]TTAGAGAAGTTATGA | 83860 |
rs374996134 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957085 | AGCAAATCAAAAGTC[A/T]TATCACTATCAACTT | 83860 |
rs375031460 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894478 | GCAAGTGTAGTGTGA[C/T]GCGTCAGTGACCTGA | 83860 |
rs375050818 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944137 | TGTGTGTGTGTGTGT[G/T]GTGGGGGGGAGGGAA | 83860 |
rs375083336 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946911 | CTCGTTAAAACTTTT[A/C]TTTTTTTAAAAAAAT | 83860 |
rs375094177 | in-del | -/AGAG | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7941104 | TTAGGTTGGAAACAT[-/AGAG]AGCCACAAATATGAA | 83860 |
rs375101452 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884511 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTAGGATTA | 83860 |
rs375125253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7923424 | GGGTGGGGTGGAACT[C/T]TAATATCTGTATTCT | 83860 |
rs375155158 | snp | A/G | 3.35576e-05 | 0.00409606 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965337 | GAAAGATGGACTTGT[A/G]AGGAAGGAGAAAGAG | 83860 |
rs375198564 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971704 | AATAAATTTCCCCTT[C/T]AAATCTCTTGAGCGA | 83860 |
rs375205130 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969706 | TCTGTTTTTACATTC[G/T]AATATGATCTGGAAA | 83860 |
rs375215497 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909197 | TCATAAATGCAGGTT[C/G]ATAACCCATTCTAGG | 83860 |
rs375230157 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921002 | GAGGATATTAGTGGC[A/G]TTCTGTTTGAGGGAA | 83860 |
rs375231262 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974167 | ACACACACACACACA[A/C]ACACAAACACACACA | 83860 |
rs375253688 | snp | A/G | 1.93624e-05 | 0.0031114 | intron-variant | TAF3 | GRCh38.p7 | 10:8009348 | GCGTACCTGCCGCCC[A/G]CGCGGTTAGCATGGA | 83860 |
rs375338860 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863450 | ACCCCGTCTCTACTG[A/T]AAATACAAAATTAGC | 83860 |
rs375339152 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7956516 | ATTTTAAAATAATTT[G/T]ACAGTCAAATGTTGA | 83860 |
rs375342126 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857910 | TTTTCAACATTTCTG[A/T]TTTTTTTTTTTTTTT | 83860 |
rs375342587 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7846013 | ACCCAGGCTGGAGTG[A/C]AGTGGCGCAATCTCG | 83860 |
rs375360615 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856557 | CCAGGAAGCCTAATA[C/T]CTGAACAACAAAAGT | 83860 |
rs375399735 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843402 | GCATGAGCCACCGTT[C/G]CCAGCTTACAGTCAT | 83860 |
rs375412353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7824133 | ATTATATTTAAACTT[A/G]ACTTTAATAATCAGC | 83860 |
rs375422450 | in-del | -/AAGAGTGC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014009 | TTAACTGCAAAACCC[-/AAGAGTGC]TTAGACTATTGTTAT | 83860 |
rs375432008 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978897 | AAGGCATTGAAAAGC[C/T]AGGTATGGTAGGCCA | 83860 |
rs375452828 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976835 | GATGAGTTTAATGTT[C/T]GTCAAGTTCCATAAA | 83860 |
rs375459509 | snp | C/T | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016884 | GATTTTATAAATGGT[C/T]TTTGCAATAATAAAA | 83860 |
rs375460266 | in-del | -/A | 0.486266 | 0.0817214 | intron-variant | TAF3 | GRCh38.p7 | 10:7994810 | TCTACTAAAAATACC[-/A]AAAAAAAAAAAAAAA | 83860 |
rs375461131 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854663 | CCTCTAATGGGGGGG[-/G]CGGGGGGAGGGGAGC | 83860 |
rs375470892 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955309 | AATAGGAAAGTTTGT[A/G]CATCATTGTAGAAAT | 83860 |
rs375474348 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907467 | AGTGAGTTCATGGCT[A/G]TTACTGCTTAGGACA | 83860 |
rs375476076 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923171 | TGCATGTTGGAGGCT[-/T]AACATTCTATATCCT | 83860 |
rs375509210 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886001 | TGGCGCGACGATGGC[C/T]CACTACAGCCTCAAC | 83860 |
rs375511661 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846079 | GTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 83860 |
rs375530053 | in-del | GTTG/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838366 | CCAGTTTTGTTTTTT[GTTG/T]TTGTTGTTGTTGTTT | 83860 |
rs375554978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7944006 | CTTTCTGCAATTGAT[A/G]TGCGTAAGAGGAAGA | 83860 |
rs375569570 | snp | C/T | 4.98509e-05 | 0.00499229 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964677 | TAAAACGATTGAGGC[C/T]TCTATCGATGCTGTG | 83860 |
rs375572717 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985679 | CTTATTGTACAAACC[C/T]GGTCTGCCGTTTGGA | 83860 |
rs375574523 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970379 | CTCTGAGGGTTTGGT[A/G]TAGTGGTTCCTGTTT | 83860 |
rs375628280 | snp | C/T | 5.21023e-05 | 0.00510377 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818799 | GGTGCAGCTCAGCGC[C/T]TGCCACCTCCTCACG | 83860 |
rs375634505 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TAF3 | GRCh38.p7 | 10:7881485 | CAGACACACACATAC[A/G]CACAAACACACACAC | 83860 |
rs375662994 | snp | A/G | 3.60933e-05 | 0.00424798 | missense | TAF3 | GRCh38.p7 | 10:8009133 | GCGCCCTCGCAGAAC[A/G]GGCCGAAGACCCCAC | 83860 |
rs375683204 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977737 | TTCTCTTTTTGCTCA[C/G]ATGGCACATGGTTTT | 83860 |
rs375688181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7859699 | GGGGCATTATGGCTG[C/T]ACTTTATTTTACTCA | 83860 |
rs375690990 | in-del | -/AA/AAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925798 | AGGAAACTCCATCTC[-/AA/AAA]AAAAAAAAAAAAAAG | 83860 |
rs375746247 | in-del | -/ACACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006180 | ACTGAAAAAAAAAAT[-/ACACACACAC]ACACACACACACACA | 83860 |
rs375756753 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999181 | TAATTCTTTTACAGA[A/G]GTGTTCTCACTGCAG | 83860 |
rs375799007 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934176 | TTTTAGGACTACCTT[A/G]ACCAACTTACTTCAC | 83860 |
rs375803124 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967491 | CGAAGCACAGAGTCC[A/G]CCTGAGAGAAAGATA | 83860 |
rs375807461 | in-del | -/TAGGC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820964 | TAGGCTAGGCTAGGC[-/TAGGC]ATAGTCCAGATTATG | 83860 |
rs375831062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986036 | TGATCCACCCACCTC[A/G]GCCTCCCAGAGTGCT | 83860 |
rs375847927 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995818 | ATTTATAGTTGTGTT[A/G]TAATTATATGAATGT | 83860 |
rs375877996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966765 | GTATTTTTAACTTCA[A/G]ACTTACCTAGAAAAC | 83860 |
rs375879809 | snp | A/C | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015866 | GAAAGTAAAAAAAAA[A/C]AACAACAAAAAACCC | 83860 |
rs375908453 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823791 | AGGCCTGCGCCACCA[C/T]GCCCGGCTAATTTTT | 83860 |
rs375915274 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884815 | CATATCCATACATAC[A/G]TCTATGTCTATTTCC | 83860 |
rs375916977 | in-del | -/TGAATCTTTCCAGGTGTTCACTTTTTTTTTTAAACCTAGAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901011 | CTGGTGTGCTTGTGG[lengthTooLong]TGATCATCCAAAAAT | 83860 |
rs375917656 | snp | A/G | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817535 | CATATTTAAGAAACC[A/G]CATAGTTCAGCCACT | 83860 |
rs375934032 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841038 | GTATTTTTAGTAGAG[A/G]GGGGGTTTCACCATG | 83860 |
rs375941676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861437 | TCTTTGCATCTATTC[C/T]TTTTGACTAGATCCT | 83860 |
rs375942507 | snp | C/G | 0.000332051 | 0.0128808 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818811 | CGCCTGCCACCTCCT[C/G]ACGGACGTGCTGCAG | 83860 |
rs375996453 | in-del | -/AAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970774 | TAGGATTTGCCCCCA[-/AAT]AATCTTTTATTAAAT | 83860 |
rs375997312 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909174 | GTATCAGCCTCAACT[A/G]GAGCTTGTCATAAAT | 83860 |
rs376032844 | snp | A/G | 3.31609e-05 | 0.00407177 | missense | TAF3 | GRCh38.p7 | 10:7964216 | GTCCATGTACAGGAC[A/G]GTACAGACTTGGCAC | 83860 |
rs376121857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7895382 | TATTTCTCTTCTGAA[A/G]CCAGCAGACAGTTCT | 83860 |
rs376148402 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008291 | TTTAGTAGAGACGGT[A/G]TTTCACCATGTTGGC | 83860 |
rs376168645 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010666 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGCAGAT | 83860 |
rs376205634 | in-del | -/AGAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941106 | AGGTTGGAAACATAG[-/AGAG]CCACAAATATGAAGC | 83860 |
rs376293070 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7968065 | AAACAAAAATACACC[C/T]GAAATGCGGTTCCAT | 83860 |
rs376297566 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008926 | GAGAGGCCACTTCAT[C/G]CAGGGCCTGGAACTC | 83860 |
rs376302392 | in-del | -/T | 0.0182996 | 0.0938879 | intron-variant | TAF3 | GRCh38.p7 | 10:8011246 | ACAATATTACATTTC[-/T]TTTTTTTATGTTTTC | 83860 |
rs376321538 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865372 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 83860 |
rs376328358 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871257 | TTCAAACAAAGGAAA[C/T]ATTAGTAATGATGGC | 83860 |
rs376346538 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009429 | AGACGCATTTCTCTT[A/C]AAAATTTTATTATTT | 83860 |
rs376384272 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011904 | GCTTACTGGCTGTGC[A/G]TGGTGTCTCACGCCT | 83860 |
rs376398667 | snp | C/T | 0.000181984 | 0.00953723 | intron-variant | TAF3 | GRCh38.p7 | 10:7965754 | AAAAGTAAGCAGTTT[C/T]TCATTTTTGGCCCTA | 83860 |
rs376477148 | snp | A/C/G | 6.64456e-05 | 0.00576359 | synonymous-codon, missense | TAF3 | GRCh38.p7 | 10:7964800 | AATTTCAGGCCCGGA[A/C/G]TGTACTACTCCCAAA | 83860 |
rs376535398 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927352 | ACATCTTCCAACATG[C/T]TGGTGGTTGGAAGTC | 83860 |
rs376538662 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925818 | AAAAAAAAAAGAAAA[A/G]AAAAGAAAAGAAAAA | 83860 |
rs376569744 | snp | A/G | 0.000120007 | 0.00774527 | missense | TAF3 | GRCh38.p7 | 10:8009166 | CCGGCCCCCGCGCCC[A/G]CCCCCGGCCCCATGC | 83860 |
rs376571453 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858497 | GTTTTTTCACTAGTT[C/G]CGGATCTTACTGATT | 83860 |
rs376585843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942245 | TTTGTCGATTTCAGT[C/T]GAGCTTCCCATATAG | 83860 |
rs376594121 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959830 | ATACAGAAAAATCCA[A/G]ATTTTCAAGTTATTG | 83860 |
rs376645296 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830144 | TATGTCCACTTCAGT[A/C]CCTGCCATTTCTTTC | 83860 |
rs376665981 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982808 | AGATGACAAAGATGG[A/T]GTCCTCCACAGCGGT | 83860 |
rs376688004 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917677 | GTTGGGGGAATGGGG[A/G]TTTGCCCCACCAAGG | 83860 |
rs376694502 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886939 | TATATTTAAGTGATA[A/C]GAGCTAGTTAAGAGG | 83860 |
rs376728822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8003779 | GGCCAGGCACAGTGG[C/T]ATGCGCCTGTAATCC | 83860 |
rs376741677 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835295 | GCTGCATTCAAAGCC[A/G]TCCTGGGCCGCATAT | 83860 |
rs376744601 | snp | A/G | 1.66402e-05 | 0.00288441 | missense | TAF3 | GRCh38.p7 | 10:7965434 | AAAGTGAAAGATAAA[A/G]GCAGAGAAGATAAGA | 83860 |
rs376770999 | in-del | -/G | 0.327211 | 0.237778 | intron-variant | TAF3 | GRCh38.p7 | 10:7858835 | TGTGTGTGCGCGCGC[-/G]CTGCATGTCACTGAA | 83860 |
rs376799538 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979940 | TTTCTTAGTGGCTGG[A/G]AAAAAATTAAAAGAA | 83860 |
rs376812976 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899721 | GATTTATGTATATGA[C/T]AGACTATTGAGTGCT | 83860 |
rs376814273 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883382 | AGAAATACCGTAGAC[A/G]GTGGTGTGTTCTTCT | 83860 |
rs376824108 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943030 | GTTGCCGTCCAGTCC[A/G]GTTTCTTTCTGTGTC | 83860 |
rs376830278 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839672 | TCTTTTCCTTTCAAA[C/T]TGGTTTCTTGAGTAC | 83860 |
rs376837630 | in-del | -/CTCT/CTCTCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957794 | GCTCTCTCTAGCGCG[-/CTCT/CTCTCT]CTCTCTCTCTCTCTC | 83860 |
rs376850942 | snp | C/T | 4.96866e-05 | 0.00498406 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8013814 | CATGATTGGGTGTGA[C/T]GACTGCGATGACTGG | 83860 |
rs376856457 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857901 | CCAGGGTTCTTTTCA[A/T]CATTTCTGATTTTTT | 83860 |
rs376870609 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922047 | ATTATGTTCGTATTT[C/G]TTTTATGTTACTTCC | 83860 |
rs376872584 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841375 | CTTTCCTAGAGCTTA[C/T]AGTCTACTTGGGGAA | 83860 |
rs376892714 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961997 | TGGGACTACAGGCAC[A/G]CACCACAACACCCAG | 83860 |
rs376948243 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003303 | TTTTTGTGTGGTTAC[C/T]CTAGAAATTACCATA | 83860 |
rs376966111 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7916717 | TTAAGGGAATCTTTT[C/T]AAAAATCCTTTTTAT | 83860 |
rs376967575 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879925 | TAAATGAAATAAAAC[C/G]TGGCTGGGCACGATG | 83860 |
rs376980031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886496 | AAAAGTTTGGTTTTT[C/G]CATTTATAGACCTGG | 83860 |
rs376981010 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969381 | ATAAATCTAACATTA[C/T]ATTTCAGAACAGTTT | 83860 |
rs376986025 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837413 | TTTGAGAGGTTGAGG[C/T]GGGCTGATCACTTGA | 83860 |
rs376986679 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7869907 | TGCTCTTTAAAAATT[A/C]TTTGCCTCTTTTATC | 83860 |
rs377010661 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898998 | TTAAAAACCATTAAT[G/T]TCAGTTCCCATAGGT | 83860 |
rs377040543 | in-del | -/CCC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006816 | GGCTGTCGTGAGCAA[-/CCC]CAGCCGTGAACATGG | 83860 |
rs377079428 | in-del | -/ATGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878691 | TAATTAATTCAACCA[-/ATGT]ATGTATGTATGTATG | 83860 |
rs377091557 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896829 | TCTAGATTCTCTCTT[-/T]AAGGTCTAACAAGGC | 83860 |
rs377104667 | snp | C/G/T | 0.000104155 | 0.00721586 | missense | TAF3 | GRCh38.p7 | 10:7964495 | CCCAAGGTCACGACT[C/G/T]ACATTCCCCAAACAC | 83860 |
rs377117838 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983181 | TGGTGCTCACAGTCC[C/T]TGGCGAAGCCCCGCT | 83860 |
rs377131024 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924550 | TGGGCATGTCTCCCA[G/T]TTTCTCTTTAACCTT | 83860 |
rs377190091 | in-del | -/ATGGGGAGATTAGGGCAGACG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957291 | AGATTAGGGCAGACG[-/ATGGGGAGATTAGGGCAGACG]GCTGAGGTGAATTCA | 83860 |
rs377193818 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987249 | TGAGCCTGGGAAATC[A/G]AGGCTACAGTGAGTC | 83860 |
rs377197234 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880762 | TTCAACTCCTTACCT[A/G]CTCATCACTAAGCCA | 83860 |
rs377206269 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967054 | TAACACACCTGTGAC[A/G]TAGGTCCAGCAGGTA | 83860 |
rs377254455 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982041 | GAAAATAAGCATTTT[A/G]TATTTTAAAATATAG | 83860 |
rs377255264 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945162 | TGGCCTCTGGCACCC[A/G]TGGCATTAGAGGACT | 83860 |
rs377260547 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7915001 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTTAC | 83860 |
rs377268845 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883949 | AACGCAGGGCATCAC[A/G]TGGCAAGGGGCTGAG | 83860 |
rs377318262 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817963 | TTTTTTTAAAAAAAC[G/T]GTTAAAATATTATCG | 83860 |
rs377341125 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954186 | GAGTGCACTCCATAT[A/G]TGAATGAGTGGATTA | 83860 |
rs377344563 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974648 | TGGGACATGAGGACA[C/T]TGGCAAGGGTTGAGG | 83860 |
rs377444334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7990851 | ACCTCCTCACAGAAG[A/G]CACCAGGCTGACTCA | 83860 |
rs377452794 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938264 | TAGGGATGGGGAGGT[G/T]TGTGGGGATAAGAAG | 83860 |
rs377457747 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924185 | AAATGTGGTGCCAGG[A/G]TATTTGAGAAAGTGT | 83860 |
rs377460073 | snp | A/G | 0.000182577 | 0.00955276 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964248 | TCCCTCACCCGAGCC[A/G]CCAATGTTGGCTCCA | 83860 |
rs377466036 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910871 | TAAGTTCAAGCCAGA[A/G]ATAATACATGCTTTC | 83860 |
rs377469639 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877743 | ATGAAGTGACTTGGC[C/T]AAGATCTTAAAAGCT | 83860 |
rs377472680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862699 | CTCCCCAGGGGGATC[C/T]CCAGGCAACCACTGA | 83860 |
rs377482079 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837757 | TGAGTCTGGGAGGTT[A/G]AGGCTGAGGCTGCAG | 83860 |
rs377496681 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956552 | AACCATTGATTGTTT[A/C]AACAAGAAGATATCT | 83860 |
rs377499644 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845959 | GGTTTGTGTGTTTTT[G/T]TTTTTTTTTTTTTTT | 83860 |
rs377502658 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939058 | GAAGATTATGGGAAA[C/G]AAGATGATTGCTCTC | 83860 |
rs377511526 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937358 | TTTGGTGTTGGCAGT[C/G]TTTCGGCTTTTGGTC | 83860 |
rs377514344 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946367 | TGTCTCTGACTGGCT[-/G]GTTTTGGTTATTCCC | 83860 |
rs377560740 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935394 | CGAGGTCAGGAGATC[A/G]AGACCATGGTGAAAC | 83860 |
rs377561796 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7906547 | TGTTTTATGAAACCT[G/T]AGAGGTTTCTGCTAA | 83860 |
rs377563183 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838908 | CTGGAGGCATTGCTT[G/T]TTTTTTTTTTTTTTT | 83860 |
rs377565403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942720 | TCCAGGGGCCCCATC[A/C]CAAGTGGGCAGCCGA | 83860 |
rs377566620 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983843 | GACCCTGTCTCTAAA[A/T]CAATAAATAAATAAA | 83860 |
rs377628932 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957792 | CACGCTCTCTCTAGC[G/T]CGCTCTCTCTCTCTC | 83860 |
rs377632877 | snp | A/G/T | 0.000133308 | 0.00816318 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964386 | AACCGCCCAGTCACC[A/G/T]GCAATGGTCGGAAGT | 83860 |
rs377680026 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7933954 | CTGTCATGACATGGT[C/T]GTCACCGCCTGCACA | 83860 |
rs377686447 | snp | A/C/T | 0.00019933 | 0.00998137 | intron-variant | TAF3 | GRCh38.p7 | 10:8013887 | TTAGGCAGCATCAGC[A/C/T]GCTCCTGAGATGAAG | 83860 |
rs377702300 | snp | C/T | 1.66007e-05 | 0.00288098 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964854 | CACAAAGTCAGGATC[C/T]ACTCCTCTGCCTCTT | 83860 |
rs377707557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820282 | ATCTTGTTTTGTAAT[C/T]ACCTGTGTATGTCTC | 83860 |
rs377709044 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959057 | AGGCAGGAGAATGCC[A/G]TGAACCCAGGAGGCG | 83860 |
rs377715977 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831162 | TTCCTCATCCACTAT[C/T]TAGTAACTTAATGGC | 83860 |
rs377744020 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846661 | ACTGAAAAAAATTCA[G/T]TCTCTTTTGCTGTCA | 83860 |
rs386740622 | in-del | -/TCA | 0.287152 | 0.247224 | intron-variant | TAF3 | GRCh38.p7 | 10:7824304 | AATTTGATTTGCTTT[-/TCA]CTTTGTTTCAGATGG | 83860 |
rs386740623 | multinucleotide-polymorphism | CT/GC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825969 | CTTCCTATCAGCAGT[CT/GC]CCAAGGGTTCCAATT | 83860 |
rs386740624 | multinucleotide-polymorphism | CG/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846119 | GCCCGCCACCACGCC[CG/TA]GCTAATTTTTTGTGT | 83860 |
rs386740625 | multinucleotide-polymorphism | CTGAGGCAGGCAGA/TTGAGGCAGGCAGG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863375 | CAGCACTTTGGGAGG[CTGAGGCAGGCAGA/TTGAGGCAGGCAGG]TCACCTGAGTTCAGG | 83860 |
rs386740626 | in-del | CC/TCCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873628 | GTTCTCCCCCCCCCC[CC/TCCT]GTCAAAAGGGGGTGT | 83860 |
rs386740628 | multinucleotide-polymorphism | CT/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902392 | TGCACCACTGCACTC[CT/TA]GCCTGGGCAACAAGA | 83860 |
rs386740629 | multinucleotide-polymorphism | AC/CT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904008 | TGTCTGAGAAGTTTC[AC/CT]GGTGCGTCTGAGTTG | 83860 |
rs386740630 | in-del | AGGG/CC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935626 | GCTAAAGCTAAGTAG[AGGG/CC]CCAGAGAATACTGGG | 83860 |
rs386740632 | multinucleotide-polymorphism | CC/GT | | | missense | TAF3 | GRCh38.p7 | 10:7965596 | GAGGAGAAAGAGAAG[CC/GT]GAAGGAGAAAGAAAA | 83860 |
rs386740633 | multinucleotide-polymorphism | AT/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979913 | ACCTGAAAGTTAAGA[AT/CA]GTGTTTTATATTTCT | 83860 |
rs386740634 | multinucleotide-polymorphism | AA/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988439 | TACTAAAAATACAGA[AA/TT]TTACACCTGTTATCC | 83860 |
rs386740635 | multinucleotide-polymorphism | CCA/GCG | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008018 | CAGCTCTAGCGACCT[CCA/GCG]GCAGCATCACCAGGA | 83860 |
rs397688381 | in-del | -/A | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7933109 | CAAACAAAAAAAAAA[-/A]TACCTGGCTACTTTG | 83860 |
rs397700862 | in-del | -/T | 0.375 | 0.216506 | intron-variant | TAF3 | GRCh38.p7 | 10:7850057 | ATTGAGTGAGAAGTT[-/T]ACAGGCTTTGCTTAA | 83860 |
rs397704861 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7864833 | TTATCTTTTTTTTTT[-/T]CCTTTTTATGTTTTG | 83860 |
rs397712339 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7877041 | ACTTTTTTTTTTTTT[-/T]CCTAATGGAGATTCC | 83860 |
rs397737727 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7929269 | TGTTGTTTTTTTTTT[-/T]GGTAATAGTCTTCTA | 83860 |
rs397743752 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881513 | CACACACACACACAC[-/AC]TAGATAGCAGGTTTA | 83860 |
rs397775983 | in-del | -/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7843659 | TCTTTTTTTTTTTTT[-/T]GAGCACTGTGATCAG | 83860 |
rs397790431 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821230 | TGGTGACTTTTTTTT[-/T]AATGCTAATTTTGGT | 83860 |
rs397796095 | in-del | -/TT | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7927982 | CCCCCACTTTTTTTT[-/TT]GGAGTTCTGGATGTT | 83860 |
rs397807741 | in-del | -/T | 0.375 | 0.216506 | intron-variant | TAF3 | GRCh38.p7 | 10:7971467 | GTTTTTTTTTTTTTT[-/T]AATGAAAGGAGTTTA | 83860 |
rs397821872 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827332 | AAGTAATTTTTTTTT[-/T]GTTAACACATTTATA | 83860 |
rs397844824 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836307 | TCTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCGC | 83860 |
rs397844830 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944134 | GTGTGTGTGTGTGTG[-/TG]TTGTGGGGGGGAGGG | 83860 |
rs397845031 | in-del | -/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832383 | AATTTCCTTCTTTTT[-/TT]AAAGGCTGAATAATA | 83860 |
rs397845444 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835330 | ATGGGCTGTGGGTTG[-/G]ACAAGCTTGCTTTAG | 83860 |
rs397845810 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898570 | AAAAAAAAAAAAAAA[-/A]TCGAACTCTTCCATC | 83860 |
rs397846179 | in-del | -/AAAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948009 | TACCTTTTATTAAAG[-/AAAG]TTTAAATTGTCTCAA | 83860 |
rs397846477 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845252 | TACCAAAAAAAAAAA[-/A]TCTCCCACTGGAATA | 83860 |
rs397846613 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996775 | ACCTCCACCTCCTGG[-/G]CTCAAGCTATCCTCC | 83860 |
rs397938371 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895728 | AATTGTGTGGCCTCT[-/T]ATCTACAGTTATAGA | 83860 |
rs397964343 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822498 | TATAGAAAAAAAAAA[-/A]TCAAAGACTGCAGAA | 83860 |
rs398012750 | in-del | -/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7885273 | TGTGTGTGTGTGGGG[-/T]GTGTGTGTGTGTGTG | 83860 |
rs398045834 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7839702 | CAATTATTTTTTTTT[-/T]AATTGTGTTTTGTTA | 83860 |
rs398045835 | in-del | -/A | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7856880 | AAAAAAAAAAAAAAA[-/A]GCAGAAAGAATGCTT | 83860 |
rs398045836 | in-del | -/T | 0.5 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7885006 | TCAGTTTTTTTTTTT[-/T]AATTTGTAGTTTGAA | 83860 |
rs398069723 | in-del | -/GTGC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828904 | TGGGTGTGGTGGTGC[-/GTGC]CTGTAGTCCCAGCTA | 83860 |
rs398069724 | in-del | -/GTTAAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857785 | GATGTTTTTGTTAAG[-/GTTAAG]AAAGAAAAAGGCAGG | 83860 |
rs398074899 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864832 | TTTATCTTTTTTTTT[-/T]TCCTTTTTATGTTTT | 83860 |
rs398096773 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869527 | CATAGTTCCCTGTTG[-/G]TGACATTTAGATTGT | 83860 |
rs527249182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864244 | ACCTATTCTTCCCTC[C/T]CTTACCCCAACCTGT | 83860 |
rs527256801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006092 | CTCAGCACTTTGGGA[A/G]GCTGAGGTGGGCAGA | 83860 |
rs527264856 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916439 | CTGTTAATTTTAAGA[A/G]TGCAAGAACTGAATT | 83860 |
rs527265223 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890275 | TCCCTTTTAAGATTC[A/G]GTTCATTTCAGATTC | 83860 |
rs527291143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961614 | TTCTTCCTTGTTCAT[A/G]TCATCCATCATGGTG | 83860 |
rs527293562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954046 | ATTCAGAGTGCACTC[C/T]ATAGGCGAATGAGTG | 83860 |
rs527308786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858285 | CAGGTCATCAAAGAA[A/G]TGAGTGATGTTACAA | 83860 |
rs527335521 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:8000088 | AGCAACAGTTTAGAC[A/G]TATACATTGTAACAG | 83860 |
rs527354318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7961102 | CCGAGACTAGGTAGA[A/G]GGTCCTTGCAGCCAT | 83860 |
rs527356726 | in-del | -/TTTTTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871454 | TTTTTTTTTTTTTTT[-/TTTTTTT]GAGACGGAGTTTTGC | 83860 |
rs527368798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012480 | GCCGTGGTGAAGTTC[C/T]TGTGCGGCACACAGA | 83860 |
rs527376306 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942936 | TCTGTGCAGGTCTTC[C/T]GCTCTTAACAGGAAT | 83860 |
rs527423218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7940024 | CAAGGCACATTATTG[C/T]GAATTAGAGGAAACC | 83860 |
rs527429962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7843998 | TATCCAATTAAATGT[C/G]AAAGAATGTTTTAAA | 83860 |
rs527435456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935116 | ACCGCATTTCTATTA[A/C]AAATACAAAAATCAG | 83860 |
rs527441882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877747 | AGTGACTTGGCCAAG[A/T]TCTTAAAAGCTCATT | 83860 |
rs527453916 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7963798 | TGTACCCTAGAACTT[-/A]AAAGTATAATAATAA | 83860 |
rs527460140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983421 | CCTGGGGAGGCAGGG[C/T]AAAGAACCTGGTTGG | 83860 |
rs527492105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830908 | TGTTGCGCATTGTGC[A/G]CTCATAATGCAGCTC | 83860 |
rs527499638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948842 | TTCGAATCTTGCTTC[C/T]TAACAGTCATTGTGT | 83860 |
rs527521078 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8000241 | CTAGCCTCAGCCTCC[C/T]GAGTAGCTAGGATTA | 83860 |
rs527529205 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854547 | GAAAGACTTCTGTGA[G/T]GTAAAGCAACTGGAA | 83860 |
rs527543459 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7823822 | GTATTTTTAGTAGAG[A/T]CGGGGTTTCACCGTG | 83860 |
rs527563024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948141 | GAACATAGTTCACTG[C/T]GACCTCGAACTCTTA | 83860 |
rs527563978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863575 | AGATCGCCCCACTGC[A/G]CTCCAGCCTGATGAC | 83860 |
rs527588772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7892215 | TCTTTTGTCTATTTC[A/G]TAAGGACTTGGCTAG | 83860 |
rs527625292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954611 | AATGAATGAATTAGT[C/T]CCAGTTAACACAGAG | 83860 |
rs527626851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857444 | AGAAGTTGGCAGGAC[G/T]CCTACAGAGTAGCCA | 83860 |
rs527642162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880068 | AGAACAAATTAGCTG[A/G]CCACCCCAAAAATAT | 83860 |
rs527679859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913771 | AGGGATACAGTAAGA[A/G]GTATACTGCGTCACC | 83860 |
rs527684354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833135 | AGGTTATTTCTGTAA[C/T]TTGGCTATTGGGAAC | 83860 |
rs527707014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872298 | TGTTTTTTAAAAGCA[A/G]TGTTCTCTGTGTAAT | 83860 |
rs527740927 | snp | A/C | 0.000672683 | 0.0183273 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818681 | GAGAGCAGTGGCAGC[A/C]AGGGCTGCGGTGGCG | 83860 |
rs527747239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976472 | CAGGCTGGAGTGCAC[C/T]GGCATGATCTCGGCT | 83860 |
rs527782883 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861001 | GAGTCTTGCTGTGTC[A/G/T]CCTGGGCTGGAGTGC | 83860 |
rs527783945 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886989 | ACCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 83860 |
rs527797829 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7984199 | TCTTATTTTTACCAC[C/G]TAGAACAATGATATA | 83860 |
rs527803640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819318 | CTTACAAGACTGGCC[A/T]TTCCTGGGCTCCTAA | 83860 |
rs527824821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859873 | TCCCAGATAACTTAT[G/T]ATTTCATAATGATTA | 83860 |
rs527849688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893378 | TTTATCACTTAAAAG[A/T]TACGTTGCTTTTAGG | 83860 |
rs527854341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8008447 | GCCAAACCCAGAAGT[A/G]AGAAAGTCTTCACAG | 83860 |
rs527856262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885744 | CAGGGATAAACACAC[A/T]CATGTTCTCTCCTGT | 83860 |
rs527856631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000956 | TCTTGGATAGACATA[C/T]CATTTGTGTGTGTGC | 83860 |
rs527891064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956112 | AATACATATGTTAAT[C/T]AGTGCATCGGGTTAT | 83860 |
rs527895715 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7837904 | TACTGATTTAATAGA[C/G]GAATGTTAATGAAGA | 83860 |
rs527896208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7844618 | CCTGACCTTGTGATC[C/T]GCCTGCCTCGGCCTT | 83860 |
rs527904235 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7991173 | CATAGATACATACAT[A/G]TATATGTATAGATAC | 83860 |
rs527909169 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979828 | GGGTGGGGTGGTGGG[A/G]TGGGGGGTGGTTCTA | 83860 |
rs527911542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886406 | TTTATTACAATTCTT[A/C]CATATTTGCCTTTAT | 83860 |
rs527925255 | snp | C/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820206 | CACTTATCACTTGCT[C/G]TAGGGAACTCATGTT | 83860 |
rs527936648 | snp | A/G | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817640 | CTGTATTTAAAAATC[A/G]AGATATTTATCCCTA | 83860 |
rs527968004 | snp | G/T | 0.000107423 | 0.00732802 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014765 | GACGACTCCCGAGGG[G/T]CTGGACCAAGCGGGG | 83860 |
rs527974025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7879329 | TGGAACTGTACACTA[C/T]TAATGAAACGTAACT | 83860 |
rs527997821 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840870 | TTTTTTTTTTTTGAG[A/T]TGGAGTTTTGCTCTT | 83860 |
rs528010170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7920348 | TGTGTGTGTGTGTGT[A/G]TAAATGCTTGGTTCA | 83860 |
rs528025079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962364 | TCACCTCCCACCCTC[A/C]TCCATCCTGCGTGTT | 83860 |
rs528044178 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983686 | CGTTAAAAGCTAAAC[A/G]TCATGAGCTGGACGT | 83860 |
rs528059389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7875522 | AACCTCCACTGAAAA[C/T]GGATGCTGTCCTTCC | 83860 |
rs528073577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7925278 | TGGTGTGGACATGTG[C/T]GTGGACCCTCTGGCA | 83860 |
rs528093239 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7980697 | CCTAGCAGAAGCCTT[G/T]CCTTGATGCTGGGAT | 83860 |
rs528134660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7829336 | GTTATTATTAAGTGA[C/T]GCCCGCACTGTATTG | 83860 |
rs528147317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917357 | AAACATTTCAGGCAC[G/T]AGGAACAGCAAGTAT | 83860 |
rs528179118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7938310 | CATGGGCCCCACTGC[A/G]CAGGAGGACAGGGTG | 83860 |
rs528193503 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7822416 | ATGCCTGTTTACATT[C/T]AGTAAGAAGAAGAGT | 83860 |
rs528194599 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829421 | ATATCATATTGTGTT[C/T]GGTTGTCACGTCTCC | 83860 |
rs528213638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987615 | ATTATGCCAAATTAT[C/T]TTCTAAAAGGCTATA | 83860 |
rs528213752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910661 | GCTGGGATTACAGGT[C/G]TGAGCCACCGCACCC | 83860 |
rs528262260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8011378 | CTCACCTCAGCCTCC[C/T]GAGTAGCTGGGACCA | 83860 |
rs528267951 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984370 | AACAAGTGGAGAGAT[G/T]ATAATCAAAGCATTT | 83860 |
rs528286886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840567 | TCTAAATTTAGAATT[C/T]GCCAGAAATTTAACA | 83860 |
rs528292213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7959839 | AATCCAAATTTTCAA[A/G]TTATTGTAACTATAA | 83860 |
rs528310249 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887232 | CCAGACTCTGTATTT[-/AA]AAAAAAAAAAAAAAA | 83860 |
rs528325395 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8010707 | AGGTCAGGAGTTCGA[C/G]ACCAGCCTGGCCAAC | 83860 |
rs528340022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958747 | CTTCATAACTTCCAC[A/G]CGCGTTACTTATTCC | 83860 |
rs528341664 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7894169 | TTGTAATCCAAAGTT[-/A]AGAGTCCCTCTCTGT | 83860 |
rs528373293 | in-del | -/GA | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7988560 | CCTGGGCAACAGAGT[-/GA]GACCCTGTCTCAAAA | 83860 |
rs528378723 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934819 | ACATCAAATGCGATC[A/T]GTTTACTAACTAATC | 83860 |
rs528419267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834995 | GAACATTATAGGTTC[A/C]TCAGTTTTTTCGAGT | 83860 |
rs528421954 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7973120 | TTACATGGGAATAAC[A/C]CCATCCACACCTACC | 83860 |
rs528441781 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902241 | TCAGCCTGACCAACA[G/T]GGAGAAACCCTGTCT | 83860 |
rs528442864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7939920 | ATCAAAGAAATAACA[C/G]AAGAAAATTTTTCAG | 83860 |
rs528462465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7989512 | GCTGTTTTAAATTTC[C/G]TATGAAATACGTTTT | 83860 |
rs528491335 | in-del | -/TTACC | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7842009 | GTGGATGGTGGGCTT[-/TTACC]AAATGACTGCCTATG | 83860 |
rs528511212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891461 | GTGCTAACTTGCACT[A/G]TGGTCCAAACTAAGC | 83860 |
rs528518566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884183 | TCAAACCGTAGCATA[C/T]TCCTTTACTGTTATT | 83860 |
rs528527311 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7840473 | ATGAGTGTTTTGATA[-/T]TTACTATAAACACCA | 83860 |
rs528530691 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888652 | GTGCCCTCACCAAAT[A/G]GAAAAGGGTCTTTAA | 83860 |
rs528544655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946185 | TTCCTATACCCTTCA[A/G]ATAAAATTCACACTC | 83860 |
rs528559179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876974 | CATCCTGATTTTCAG[A/G]TCTCTCTTTGAACTT | 83860 |
rs528559620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7836243 | TACATCCACCTCTCA[A/G]ACCCTGCAACCAGTT | 83860 |
rs528573301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884675 | TTACAGGCGTGCGCC[A/G]CTGCGCCTGGCCTGC | 83860 |
rs528577565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996932 | CTCCTGAGCTCACAC[A/G]GTCTGCCTGCCTCAG | 83860 |
rs528598860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004781 | TTTTTATTTATCTTG[C/G]CTAGGGTGTGTTGGG | 83860 |
rs528602436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7952435 | AACCAAAAAGAAGCA[C/T]TCAGAATGCTTGTGT | 83860 |
rs528603020 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943119 | GATCAAAGGAGTCCA[A/G]TCCTGTGGTTCCGGT | 83860 |
rs528615832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960372 | CAGGGGTCAGCAAAC[G/T]TTTTTTTGTAAAGAG | 83860 |
rs528619511 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951602 | AGCCACCCAAAATCA[C/T]GTCCACCTCTTGATG | 83860 |
rs528653078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8005159 | CCTTTGCCTTTTATT[A/G]TTTTTTTAACATTGT | 83860 |
rs528661367 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7974901 | CAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 83860 |
rs528663171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926855 | GTAAATTTACTTTAT[C/G]GTAACAACTTTTTGT | 83860 |
rs528711146 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982515 | GTGATTCTCCGGCCT[A/G/T]AGCCTCCCAGGTAGC | 83860 |
rs528719676 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880221 | CCAGCCTGGGTGACA[A/G]AGTGAAACCTTGTCT | 83860 |
rs528721409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7974212 | TAACTAGTTATGCAA[A/G]GGTCTTGCTCCACCC | 83860 |
rs528723056 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877571 | TATGGCATTTATTGT[C/T]AGAATTTTCCAATAT | 83860 |
rs528740876 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7897646 | CTCCTAGTTCCTATT[C/T]TCTCTCTCTCTCTCT | 83860 |
rs528743845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7848411 | TTTCATTTCCTTTCA[C/T]GTACAGTGTGTTCAG | 83860 |
rs528761831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856576 | AACAACAAAAGTTCA[A/G]AGCAGAAGCCTAGGA | 83860 |
rs528766308 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917723 | AACAAGCAGTTGTGC[C/T]ACTGGACTAGATACG | 83860 |
rs528796375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990439 | ATTTGTATCTGCTTT[A/T]TATGGAGGCTGCCTT | 83860 |
rs528847060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868433 | AGGAGTGGAGGCAGT[A/G]TGACATAGCAGCCAA | 83860 |
rs528850103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910853 | TTTTAAAAAATAGAT[C/G]AATAAGTTCAAGCCA | 83860 |
rs528857026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822453 | TTTATTTATTTTCTT[G/T]TTTTAATGCATCACA | 83860 |
rs528914090 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7941028 | GTGGAAAGCTCATGA[-/C]CTGTTGAAGTGGTGC | 83860 |
rs528919334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823016 | TACTCAGAAGGTGAA[A/G]GTAGGAGGATGGCTT | 83860 |
rs528938300 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959959 | GAGCAGTTTCCCTCT[G/T]GTCTCCCAGTATCCA | 83860 |
rs528955335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7973253 | ATGGGCCAAACACAC[A/G]ACTCAATAATAGTAG | 83860 |
rs528974801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863090 | ACCTAGGAGTCTGAT[A/G]TCTTCTGTGAAAATC | 83860 |
rs528977780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7932556 | ACCAGTCAAAACAAA[C/G]CATTCCTGTATTCTC | 83860 |
rs528997072 | in-del | -/A | 0.302184 | 0.244493 | intron-variant | TAF3 | GRCh38.p7 | 10:7958492 | TGTTGGGTAAAAATT[-/A]AAAAAAAAAAATTAT | 83860 |
rs529001326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904879 | GCTCCCTTTAGGCTG[C/T]ACACATGAACCCCAA | 83860 |
rs529023746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856681 | AACAAGGGCTCCTTC[A/G]AAAAATGGCTTTTTC | 83860 |
rs529036181 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922440 | CTGTAAAACATAGAT[G/T]ATTATCAAGTGATAT | 83860 |
rs529045924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005464 | ATTCATGCCATTCTC[A/G]TGCATCTTTACCTTA | 83860 |
rs529053183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882716 | TGAGCAAGCTTTGCA[A/G]AGTGATCACTTGATG | 83860 |
rs529089368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841886 | TTTATTTATTTTTTT[A/T]AAATAATCAGGTAGA | 83860 |
rs529122319 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7883359 | AATTCAGGGTGATTA[G/T]TTTCATCAGAAATAC | 83860 |
rs529142742 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7970072 | AAGAGCAGTTTGTGT[C/T]ATTTAATTAAGATAA | 83860 |
rs529154324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925349 | ACCACCTTGGCTTTG[C/T]ACTCACCTTGGCTTA | 83860 |
rs529154737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835418 | CGGAATGTTCCAAAT[A/G]TGGGAACTTGCTCAC | 83860 |
rs529156399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960562 | AGACATTTCAGGCAC[A/G]GGGAATCGCATGTGC | 83860 |
rs529157800 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957192 | GCATTAATACCTATC[C/T]AGAACTACCTTTCCT | 83860 |
rs529181395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917410 | GCTGTGCATGAGAGG[A/G]AGTGAGCTTTGTGGC | 83860 |
rs529198055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8011426 | AACTGGCTGTTTCTT[A/G]GCTGTTTTTGTTTGT | 83860 |
rs529207772 | in-del | -/AAAA/AAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837341 | TGCTCCAGTCTGGGC[-/AAAA/AAAAA]AAAAAAAAAAAAAAA | 83860 |
rs529237541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966496 | AGGCTGTGACCTCTG[C/T]TTACCCAGCTTTGCT | 83860 |
rs529245211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934498 | CACCCAGGCTGGAGT[A/G]CAGTGGCACGATCTC | 83860 |
rs529269571 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7940761 | GGAGTTTGAGACCAG[C/G]CTGAGCAACAGAGCA | 83860 |
rs529281201 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853164 | ACACAGCCTTTATTT[A/T]AAAAAATCATATAAA | 83860 |
rs529324297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877874 | TTATACACCGTGTGT[A/G]TTATTTTGAGAAGGG | 83860 |
rs529333559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7940025 | AAGGCACATTATTGC[A/G]AATTAGAGGAAACCA | 83860 |
rs529340359 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7885545 | CACTTGGCCCCATCC[A/T]CTGCTGTAGGCAACC | 83860 |
rs529369179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878459 | AGGAGGGAGGGGTGA[C/T]GGGAGGAGTAAGGGT | 83860 |
rs529372846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918973 | AGAAGAAGAAATTGC[C/T]ACCAGTTGAGGGGGC | 83860 |
rs529373720 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928097 | ATTAAGAGCTCTTCC[A/G]TTTGTGCCTATTTTA | 83860 |
rs529388610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869972 | TTACTGAACTACTTT[C/T]GACCCCAAGTTTTGC | 83860 |
rs529396441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946834 | TATCACAATGATTAT[A/T]ACAACTTTTTTTGTA | 83860 |
rs529410387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7995791 | AGGCCACGAGCTTCA[A/G]GAATTAAATCCATTT | 83860 |
rs529417317 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7953887 | AACACAGAGCTCTCC[A/C]TAGTGAGATTCAGAG | 83860 |
rs529449528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905421 | TTTGTTTTCATACAC[A/G]ATGAAAATGTAAGTA | 83860 |
rs529458409 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011133 | TGCAGACTGTGATGT[A/G]TTAGCCTACTGGTGG | 83860 |
rs529468739 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7857282 | GCCACAGCTCACTTA[G/T]AAATGTAATCTACAT | 83860 |
rs529484125 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008028 | GACCTGCGGCAGCAT[C/T]ACCAGGACAGAAGCT | 83860 |
rs529498493 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836250 | ACCTCTCAGACCCTG[C/G]AACCAGTTGCAGTTG | 83860 |
rs529501358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967348 | GTTTCAACAGCCATT[A/G]TGAATTTGAGTGAAG | 83860 |
rs529518273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975530 | TCTTTGGCATCACTC[A/G]GTGCTCTAGGGGATG | 83860 |
rs529529735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850180 | ATTCTTAGTGATGTA[C/T]CTGTGGATTAAATCT | 83860 |
rs529550844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7880723 | TTTTTAGTAGTTTCT[A/G]TTCTGACCACCAAGG | 83860 |
rs529577675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983205 | CCCCGCTTCCCGGGC[C/T]TCCGTTATCAGCCCC | 83860 |
rs529636189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986333 | GAACCAGCAGCACCT[A/C]AAAAATAGCATTTCC | 83860 |
rs529691549 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881081 | TCTCTACAAAAAATA[C/G/T]AAAAATTAGCCAGGT | 83860 |
rs529707599 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7833945 | AGATCTTGCCATTCC[C/T]GCTGGGCACCATGGC | 83860 |
rs529724657 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7950020 | GATACATGGTGAAAT[C/T]GTTTCTCTCATTTTT | 83860 |
rs529724776 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7942950 | CTGCTCTTAACAGGA[A/T]TTTGACCTTCGTCAC | 83860 |
rs529737755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873454 | CGAGATGGTTGAGGA[A/G]CCTGTCATGTAATTT | 83860 |
rs529756410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994341 | CTGATGATGAATGGT[A/G]TTTAGGAATCATAAT | 83860 |
rs529757579 | in-del | -/AAAGG | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005813 | AACTTTGAACTCCTA[-/AAAGG]CATTACATGCCTTTT | 83860 |
rs529760347 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929894 | AGAAATTACATGTCT[A/G]TATAAGTATTCAAGA | 83860 |
rs529765066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826873 | TCATGGGTACAGCAT[A/G]TTAGAAAGTTCCTGG | 83860 |
rs529792320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881631 | CTTCTATTTCTAGGG[A/G]GCCCCTTGAAATTTG | 83860 |
rs529801930 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016909 | ATAAAACCAAAGAAT[C/T]ATTTTCAGGGGGCTG | 83860 |
rs529811237 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875119 | AAACCAATCTTCATA[C/T]TGATTTTATGTATTC | 83860 |
rs529817627 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7993376 | TAGAGATGGGGTCTT[G/T]CTGTGTTGCCCAGGA | 83860 |
rs529819914 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954662 | AGTGCACTCCATATG[C/T]GAATGAGTGGATTAG | 83860 |
rs529821507 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901396 | ACAAAGAAATTAATT[A/G]TCCAGTATGAAAACA | 83860 |
rs529821602 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967924 | TACAAATAGGAAAGG[A/T]TAAAGGTTAGGACAA | 83860 |
rs529823616 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872623 | ATCTTGCTTTCAGGT[A/G]CCCTGAATAATAATA | 83860 |
rs529830647 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830228 | CTATCTAAATGGTTG[A/T]TCTGAAGGAAATTTA | 83860 |
rs529833234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834438 | ATCCAGTTGTCTCCA[C/T]GCTGGGAAATAGCAT | 83860 |
rs529837068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7971102 | CAGCCTTTCTGACTC[C/T]ACACTCTGAGCACGG | 83860 |
rs529847117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923664 | ATTCAATAGAGTAGC[A/G]GATACCTGATGGCAA | 83860 |
rs529893029 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827123 | GCAGCTGGAGCTGGC[A/G]AGTGTGCACACATAG | 83860 |
rs529904100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860523 | ATGGAATTATTTCGA[A/G]ATACTTCCCCTCATG | 83860 |
rs529905297 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7845639 | GTGAGTATTATAGCA[C/G]TATCTGATCAGATTT | 83860 |
rs529959770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979072 | AAAGGCAGCCAGATG[C/T]GGTGGCTCACGCCTG | 83860 |
rs529984410 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953164 | CTCAACATTCCATCA[C/T]GTTGTTTCACTTCGG | 83860 |
rs529991777 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972562 | GATGAAACTTTGAGC[C/T]GAGATAGCAGGTTGT | 83860 |
rs529994651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937550 | GGTTCATTTTTTTGT[C/T]GTTGAGTTTTAAAAT | 83860 |
rs530017288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986976 | ACATCTCACCCTTCC[C/G]CCAGGTTAATCACTG | 83860 |
rs530024052 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863685 | CACATATATATATAT[-/AC]ACACACATATATATA | 83860 |
rs530028846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7895115 | GGTGATCCGCCTGCC[C/T]CGGCCTCCCAAAGTG | 83860 |
rs530047595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951066 | AAAACAAGGGTATGC[A/G]TCGATTAGCTGATGA | 83860 |
rs530060291 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976896 | ATCGCAGTTTTTTCT[A/G]TTTATATTAAGTCTG | 83860 |
rs530060567 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946480 | TGTAATCCCAGCACA[C/T]TGGGAGGCCGAGGCA | 83860 |
rs530062440 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:8004330 | TGGGATTACGGGCAT[A/G]AGCCAATGTGCCTGG | 83860 |
rs530073759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7973985 | ATACAAAAAGTAGCC[A/G]GGCATGGTGGCATGC | 83860 |
rs530111609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957565 | CTGGTCTTATTGATC[A/G]AGGAACTAATGCGCC | 83860 |
rs530112105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855345 | GCCAAACAAAGGGAC[C/T]GTGGGTTGAGGCCTG | 83860 |
rs530127616 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009225 | GCTGCTCGCCCAGGC[A/C]GCCGCGGGCCCTGCC | 83860 |
rs530164712 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7847919 | AGACTACAGGCACCC[A/G]TCACCACACCCAGCT | 83860 |
rs530169296 | snp | A/G | 1.6943e-05 | 0.00291053 | missense | TAF3 | GRCh38.p7 | 10:7964451 | AGAAATCACCTGGAC[A/G]TTCCAAGAGCCCCAA | 83860 |
rs530179235 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997455 | CTCTGTGCAGCTGGG[A/G]AGGTGAGGACGGGCT | 83860 |
rs530192680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931863 | ATTGTTTTGTTGTCT[A/T]TGGCCTCATGGATAA | 83860 |
rs530243865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841142 | AGGCGTGAGCTGCCG[C/T]GCCCGGCCTAGAGCT | 83860 |
rs530273485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996673 | TATCTGTATTCTTAC[A/G]TTGAGGCAGGGTCTC | 83860 |
rs530273803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7874278 | TAAACTTGTACTGAT[G/T]AAGTTTTAGAGGCTA | 83860 |
rs530274668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987879 | GCTATTCCCAGATCT[C/T]TTCTGAAATCTGTAG | 83860 |
rs530279301 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904833 | GACACGGGGCCGACC[A/G]TAACTGGCTGAGCTC | 83860 |
rs530294110 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7988440 | ACTAAAAATACAGAA[A/T]TTACACCTGTTATCC | 83860 |
rs530315018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827640 | CAAATATTAGCTGGG[C/T]GTGGTGGCGGGTGCC | 83860 |
rs530331093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996058 | CTAAGTTAGAAAAAT[C/T]GAACACCTGGTGTGT | 83860 |
rs530339768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938376 | TTTAGTTCAGGGGCA[A/G]TGTGATGGGCGGGCC | 83860 |
rs530364300 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859135 | GGCGTGTGGTGGGCA[C/T]CTGTAGTCCCAGTTA | 83860 |
rs530369031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7854605 | CCTGAACCTGGACCT[C/T]GAAGGATAAGATTTA | 83860 |
rs530369153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7948228 | CCACTGGGCCCTACT[A/G]ATTTTTTTTTTCTTT | 83860 |
rs530374405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916270 | AATGTATGTATTTCT[A/G]TTTTTGACCATGTTT | 83860 |
rs530378743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820575 | TCTTAGCTCTCTATA[G/T]CCTCGAACTTCAGGG | 83860 |
rs530386719 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979466 | TCCCCCTCAATAAAT[C/G]ACTCATACACCTGAG | 83860 |
rs530387194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7930581 | TGGGAACTTAATTCT[A/G]TATAGTAGCTGGCAG | 83860 |
rs530399954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945507 | TTGGTATCTTCCCTT[C/T]TTCTAGTTAAGTGGA | 83860 |
rs530416019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834491 | TAAGGGATACTTATT[A/G]TATATAACTCGGTTG | 83860 |
rs530416515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979150 | GAGATCGAGACCATC[C/T]TGTCTAACACGGTGA | 83860 |
rs530426552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923694 | AAACTTTTTTGAAAA[A/G]AGTACCTCCCTGCTT | 83860 |
rs530449509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937710 | ATCACACACACAGGT[C/T]ACAGGGAATAGTAAT | 83860 |
rs530460945 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833849 | TCCCTTCCTGGGGAC[C/T]GAGGGCTTCCTGGGG | 83860 |
rs530462259 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919538 | AGCACCAGTGGGAAC[A/G]GGGTTATAGTACGGT | 83860 |
rs530469991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951539 | GTGCAGCCGCTTTCC[A/G]TGCCTCTGCTTCTGT | 83860 |
rs530477276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7827766 | GCCTGGGTGACGGAG[C/T]GAGACTCTGTCTCAA | 83860 |
rs530483352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881659 | TTGATAGAGTAACAA[C/T]CATGCATTTAGATGT | 83860 |
rs530484945 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007181 | ACCTTTGGCTTACTA[A/G]TACCATGGAATACAA | 83860 |
rs530502343 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835804 | TGCATAGATGCCTCA[C/T]ACTCGGGTCTCATGG | 83860 |
rs530536030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7828202 | TGAGCCTGTGAATGC[C/T]CACTGCACTTCAGCC | 83860 |
rs530545911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882416 | ACAGAGGAAATAATT[A/G]TTACAGGGATGAGAA | 83860 |
rs530567577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943613 | AAGAATAAATACTTG[G/T]CATTTCCTCTGAGCT | 83860 |
rs530579049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987100 | GCCAAGGCAGGCAGA[C/T]CACTTGAGCCCAGGA | 83860 |
rs530595630 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7895187 | ATGAGGGGCAATTTC[A/C]TTGGTAACTTGATAA | 83860 |
rs530598861 | in-del | -/TATG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998262 | ATATATATATATATA[-/TATG]TATATATATATATAT | 83860 |
rs530613369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944400 | TTAGTCAGTAAGACC[A/G]TCAACAGACTAATTA | 83860 |
rs530619999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7846116 | GGCGCCCGCCACCAC[A/G]CCTAGCTAATTTTTT | 83860 |
rs530631108 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885278 | CACACACACACCCCC[A/C]CACACACACAAAGTG | 83860 |
rs530635375 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852007 | CAGGTTGGTCTTGAA[C/G]TCTCGGGCTCAAACG | 83860 |
rs530639441 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877937 | AGATCTCAAATACAT[C/T]GGAGCTAATGTTTCT | 83860 |
rs530643286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7986387 | CGCCAGTGTGGTTCT[C/T]CTTCTTTTTCGTATA | 83860 |
rs530657305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916406 | ATTTTAGTTAGCTAT[A/G]AAGTTGGATAAATAT | 83860 |
rs530678201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950770 | CCTTTGGTGTCAGCT[C/G]TCGCACTATAAGGAA | 83860 |
rs530712293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902462 | TCTTTTCTTAGGAGA[A/T]GTTATTAAGAGTCCG | 83860 |
rs530713154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931583 | CAGACCACAGATTTT[C/G]ATGAAGGTTCTAAAA | 83860 |
rs530728179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854408 | TGCGAGCCGCAGCGA[C/G]ATACACACATGGAAG | 83860 |
rs530763511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887919 | CTCCAATCCACAGAC[C/T]AGCAATATCAGAATA | 83860 |
rs530768805 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990156 | GTGTGTTATAACCCA[A/C]CTGAGAAATGCTGCT | 83860 |
rs530786699 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951466 | AGGCTAACCTGGGCT[C/G]ATTCCTGTGGCAGTG | 83860 |
rs530801487 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7972208 | AAGTGCATGTGAGAA[A/T]TTATTTTATGATTGT | 83860 |
rs530824386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7945532 | AGTGGATTCCCTTTG[A/G]CCGCAGACACTCTCT | 83860 |
rs530857473 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7945939 | TGTTTGTTAACCTCC[C/G]CATTGCCAGGCGGAC | 83860 |
rs530858572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996251 | GAGGGTAGAGAAGCC[A/G]CTTCAAGCTCACGCA | 83860 |
rs530864330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840443 | AAGCATGAGCCACCG[C/T]GCCCGGCCTGGAAAA | 83860 |
rs530883189 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981458 | ATAAATATCTCATAA[C/T]ATATTGGATCAGGTG | 83860 |
rs530886606 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7951586 | CCAAAGCAAGTCACA[C/T]AGCCACCCAAAATCA | 83860 |
rs530887001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946155 | AGATCAAACTATTTT[A/G]AAACTACCGGTGACT | 83860 |
rs530891242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7959410 | CTATTCCTTTAAATA[A/G]CATAAAGGAATGAAT | 83860 |
rs530895264 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920223 | CACACCACTGCACTC[C/T]GGCCTGCGCGACAAA | 83860 |
rs530897509 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948712 | AGACAGGGATAGATA[C/G]ATAACAACCAAAAGC | 83860 |
rs530899786 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922529 | AACGTGCTGATTAAT[A/G]AAGTAAGTTGTTCTT | 83860 |
rs530913688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883478 | CTTCCAGATTTCTCC[A/G]TTGTCAAGTTATTAC | 83860 |
rs530916048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897524 | TTCATGCGTGTTTTG[C/T]TTTTTTCATGGTACC | 83860 |
rs530920306 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7996711 | GATTTTTTTTGAGAC[A/G]GGGTCTCAGCCAGAC | 83860 |
rs530953484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958699 | CTCTTCTGAAGCAGG[A/C]GATGGCCTCGCAGGT | 83860 |
rs530959443 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973227 | CATTATTGGGTGTTA[C/T]GGTAATAAAAATGGG | 83860 |
rs530973203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890097 | GGTAAGACCTTTCAT[A/G]AACCGGCTTCTGCCC | 83860 |
rs530983605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004031 | AATATTTTTAAACTT[C/T]TCAGTTTTATTTTTA | 83860 |
rs531003891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973340 | AAAGGTTATTGGAAT[G/T]CGTACATGCTAGTGT | 83860 |
rs531006402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981486 | GTGATATTGGAACCA[C/T]TTGAGATGCCTTTCA | 83860 |
rs531069789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981007 | ATTTTAGGGACAGGG[G/T]CTGTTTGGATGGAAC | 83860 |
rs531094707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7855436 | AATGTGAATACACCG[A/G]ATGCCGAGATGTCCA | 83860 |
rs531095105 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7867440 | TAAATTACAGCTCGC[A/C]AATATTTCCTGATTC | 83860 |
rs531100251 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901732 | TAAATTAATATTTTA[C/T]ATTAAGACGCTTCAG | 83860 |
rs531114317 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925287 | CATGTGTGTGGACCC[G/T]CTGGCAGGTCAGGCG | 83860 |
rs531116291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7910002 | GTCTCCAGGTTACTT[A/G]TAATTAATATAACAT | 83860 |
rs531127872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896595 | GACAGATTTAGCTAA[A/G]TTGCAGTAAGTGGGA | 83860 |
rs531155561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7847538 | AAGCCCTGACTTCCT[C/G]GGCTCAAGGGATCTT | 83860 |
rs531173171 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961730 | GGCATTGCAGACTAA[A/G]TGTTCATCAAACTCT | 83860 |
rs531216029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7955004 | GCACTCCATAGGTGA[A/G]TGAATGAATTAGTCC | 83860 |
rs531245304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7893485 | CATCAGAATCCCTTA[C/T]AAGATTTCCTCTTAC | 83860 |
rs531245562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904149 | TGAATTCAGCGGCAG[C/T]GAGAGCCTGTTCAGT | 83860 |
rs531249598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7999867 | TGCACTCAACTTAGA[C/T]GCACTCGATTGTGCA | 83860 |
rs531254852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006862 | TCCCATCTGGATGCA[A/G]TTTTTGAAGTGTTTC | 83860 |
rs531256019 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7866318 | GCTAATCATCCAAAT[-/AAG]AAGATGAGAGATGAG | 83860 |
rs531263344 | in-del | -/ACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939618 | CACACACACACACAC[-/ACAC]CTCTACCTACACCCC | 83860 |
rs531275866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962181 | AAATTGTGTTTGAGT[C/T]CTTGCTCAAGTCTTA | 83860 |
rs531299278 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918717 | GGATGTATTATATTC[C/T]GTAGACCGTATCTCT | 83860 |
rs531389775 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890851 | AAGCTTTCGATTTAG[A/C/G]TTTCCTTAGAAATAA | 83860 |
rs531407118 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7954635 | CACAGAGCTCTCCAT[A/G]GTGAGATTCAGAGTG | 83860 |
rs531416376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864302 | CATAGTTTTACTTTT[C/T]TCAGAAATTAATTGA | 83860 |
rs531425409 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999659 | CTGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 83860 |
rs531433942 | in-del | -/TTTT | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8000897 | TACCTTCTTGTTTGC[-/TTTT]TTTATTTTCTTAGAA | 83860 |
rs531438802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894147 | GCCATTCTAATGGAA[A/G]CAGGGGTTTGTAATC | 83860 |
rs531439099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7916902 | AATTGACAAAAAGAA[A/G]TGTAATTGGGTTCGT | 83860 |
rs531443127 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8006191 | AAATACACACACACA[A/C]ACACACACACACACA | 83860 |
rs531444476 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848765 | TCTGGAAAAAATAAA[C/G]TTTATGCCTAAAGTT | 83860 |
rs531455025 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871902 | CTAATATTTGTTCAT[C/T]ACTTAAAATAAACAT | 83860 |
rs531478252 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7858467 | CAGGGGTTGTTCTTG[C/T]ATCTATACTTAACTG | 83860 |
rs531494065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928320 | ACTTAAGTATTTTTT[G/T]AGTGAGCTAATTGAT | 83860 |
rs531494770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936090 | CGTAAAACAGAGAGA[A/C]GACGTGACTCTAACC | 83860 |
rs531525800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912911 | GTCGGTGTCTGCTCG[G/T]GCTGCCATCACAAAA | 83860 |
rs531527212 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7976508 | TAAGCTCCGCCTCCC[A/G]GGTTCACACCATTTT | 83860 |
rs531532425 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7974334 | CTAGGGGGAAGGGGC[G/T]GTTTGTGGGCAAGTT | 83860 |
rs531555647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7948993 | CGCAGAGGTGCTGGG[C/T]GGGTGGGGAGCAAGA | 83860 |
rs531558627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935747 | GGTCCACTGGGGAAG[C/T]ACATTCCAAAGAGAG | 83860 |
rs531572692 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817954 | GGATTTGGATTTTTT[A/T]AAAAAAACTGTTAAA | 83860 |
rs531585572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819420 | GAACGACATCTCCAT[C/T]TACTGTTTTTCCAAG | 83860 |
rs531590060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914932 | CTCGGTGCTCCCAGC[A/C]TTTTTTTTTTTTTTT | 83860 |
rs531591427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913604 | ACTTGTGTTCTCCAG[C/T]TTGTTGGCATCCTTT | 83860 |
rs531592532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984336 | TTAGGTTTTCAGAAA[C/T]ACTTTTACTGCACAG | 83860 |
rs531620428 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999026 | GGGAATGACTAGGTG[G/T]CTGAGGAAGTGGAAT | 83860 |
rs531627578 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014835 | TGGTGCAAGTCTGCC[A/G]TCACATCCACCCCCA | 83860 |
rs531637963 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818510 | GCGGCCGTCCAGCGG[A/G]AGGCGGAGCGAGTCC | 83860 |
rs531649096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908534 | ATCTGGCATTACCCA[A/G]CACCATCATGGTCAC | 83860 |
rs531660304 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841084 | TGGAACTCCTGACCT[C/T]AGGTGATCCGCCCAC | 83860 |
rs531693356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873243 | AGATTTTTTTTTTCT[A/G]ACTTTATGAAATACT | 83860 |
rs531699646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008009 | ACAGTACCACAGCTC[C/T]AGCGACCTGCGGCAG | 83860 |
rs531730383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902039 | GACACTAACTCCGCA[C/T]CCCACGTTCGTCAGT | 83860 |
rs531741996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963014 | GCTCAGAGAGGTTGA[G/T]AGAGTCCCTAAGGCT | 83860 |
rs531743603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865705 | CAGGCAGGGGTGAAG[A/G]AAAAATAGAAAGTTG | 83860 |
rs531744296 | snp | A/G | 1.67674e-05 | 0.00289541 | missense | TAF3 | GRCh38.p7 | 10:7977243 | CTAACTTCCACAGAT[A/G]AAAGTGGAACCAGTC | 83860 |
rs531748727 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016418 | GGAGCACAGGGTGTC[A/G]TTGCCCTCGTTGTTC | 83860 |
rs531771169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819900 | TCCACAGGGCTGCCA[A/G]AATAATCTGTCCATA | 83860 |
rs531823012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7950115 | GGCAGATGTGGTTCC[C/T]GTATCAGTGAAGCTT | 83860 |
rs531824184 | in-del | -/TG | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7985819 | GACGGAATCTCACTC[-/TG]TGGCCCAGGCTGAAG | 83860 |
rs531836194 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968463 | GGGCTTTGGAATCCA[G/T]CAGACCTGGAATAAG | 83860 |
rs531837870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880092 | AAAATATAACAAATT[A/G]GCTGGCCTTGGTGGC | 83860 |
rs531855593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8001801 | AACTATACCATCCAA[C/T]AAGTCATAATTGAGC | 83860 |
rs531871181 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823020 | CAGAAGGTGAAGGTA[A/G]GAGGATGGCTTGAGC | 83860 |
rs531919605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008570 | AGCAGCTTAGGCCAG[A/G]TTAGGTTTATGGTAA | 83860 |
rs531925319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994618 | CCTCCCAAAGTGCTG[A/G]GATTACAGACTGAAC | 83860 |
rs531934253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832740 | TTTTTAGTAGAGATG[C/T]GATTTCACCATGTTG | 83860 |
rs531934286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839110 | AGTTACTTGCCCCTC[A/G]TTGCTTCGTGCTTTA | 83860 |
rs531957483 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993242 | GGAATGCAGTGGTAC[A/G]ATCATAACTCACTGC | 83860 |
rs531993020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949457 | GCAACAGCCAAGCAG[A/G]CCCCCACCTGTCCTA | 83860 |
rs532025778 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967027 | AGATCCATACACCTT[A/G]TTTTCTCCTCCTAAC | 83860 |
rs532026978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7822387 | ATAGCTTTAATAGGA[A/G]TAGAAGAGATGAAAT | 83860 |
rs532058129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000889 | TACACTCATACCTTC[A/T]TGTTTGCTTTTTTTA | 83860 |
rs532059921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922527 | ACAACGTGCTGATTA[A/G]TAAAGTAAGTTGTTC | 83860 |
rs532079765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839169 | TTCCCAAAAATAACT[A/G]TGTACCTGGGTCAGC | 83860 |
rs532092871 | snp | C/T | | | missense | TAF3 | GRCh38.p7 | 10:7964994 | CTTATATCTCTTCTC[C/T]GTCAGTGTCTCCTCC | 83860 |
rs532160114 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976483 | GCACTGGCATGATCT[C/T]GGCTCACTGTAAGCT | 83860 |
rs532164613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978353 | CTTCTGTCAGTTCCA[C/T]GTGTAGTGCAAAGAA | 83860 |
rs532168158 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7864817 | TTTAAGGAAATATAG[C/T]TTATCTTTTTTTTTT | 83860 |
rs532175237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7895043 | ACCATTCCTGGCTAA[C/T]TTTTGTATTTTTAGT | 83860 |
rs532181464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992416 | TGTTAATTCTCTCAG[A/G]AGCATAAGTAAATAT | 83860 |
rs532188706 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818555 | CAGGCTGGCGCGCTC[C/T]GTGCTGCTGGGGCTT | 83860 |
rs532199151 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7858917 | CCATTACTGCTGGCC[G/T]CTTCAGCGTCTTCTG | 83860 |
rs532214746 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830299 | ATCTCAGAATAGCTT[C/G]TATGTGCCCAACCCC | 83860 |
rs532233056 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828073 | GAAGTCACGCTATAA[G/T]GGGAATCGGTGTCAA | 83860 |
rs532235250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986157 | CCCCCTTCTTTTCTT[C/T]TTGCCCTTGGTACAG | 83860 |
rs532254617 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8007823 | AACCTCTAACTTCTT[A/G]TAGGTCCTCAATAAA | 83860 |
rs532259641 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859821 | ATGGTGTACAGTGCC[G/T]AGTAGGCACTTAGTA | 83860 |
rs532261397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852230 | GCTGGGATTACAGAC[A/G]CCTGGCACCTAGCTA | 83860 |
rs532268032 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7839549 | GACAGTGGGATCCCA[C/G]GTTTCATAGTCTTGG | 83860 |
rs532277460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833397 | TTATAGCAGCCATTC[C/T]AACAGGTGTGAGGTA | 83860 |
rs532322463 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7969871 | TCGTTATTCACCAAC[C/T]TCCCATCCTCGCAGA | 83860 |
rs532322653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914192 | TGTGGTTATACATAT[C/T]CTTAAAATACCTTTT | 83860 |
rs532328936 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831038 | GTTAGCAGTGCTGAT[A/G]CTCAGTGCCTAGATC | 83860 |
rs532335758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7907053 | GGGTGGACAGTGTTC[A/G]TAGGGCCACCTGGCT | 83860 |
rs532337797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8001837 | CTCAATTGCACATGC[A/G]TAATTATTGCATAGT | 83860 |
rs532339632 | snp | A/C | 7.63291e-05 | 0.00617727 | missense | TAF3 | GRCh38.p7 | 10:8009157 | ACCCCACCGCCGGCC[A/C]CCGCGCCCGCCCCCG | 83860 |
rs532357724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7902198 | GGAGGCTGAGGCAGG[C/T]GAATCACTTGAGGTC | 83860 |
rs532362358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860739 | TCTCAATTATTGTCC[A/G]TATTGGAGTCCAGTT | 83860 |
rs532379626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819113 | GAGTCGGGTCTTCGC[C/T]CCCAGCTCCACACCC | 83860 |
rs532399693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907804 | TTGGTGAGTGGGCCA[A/G]TGATTAGATCTGTGT | 83860 |
rs532401551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7900481 | GGCTGGAGAGAGCTC[A/G]GAGGCCCAGCTATCC | 83860 |
rs532425513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943505 | AAACCTCACACCATG[C/T]TTCATTGTCCTTGCC | 83860 |
rs532428491 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939192 | TTTTTAGTAAACTCA[A/G]CATTTTAGTTTATTG | 83860 |
rs532452454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893591 | GTTGCTCCACCTCAT[A/G]TTTTGTCCCATCTTT | 83860 |
rs532478020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895925 | AATCAAGTGCCTTCA[A/G]TGAACACCGAAGCTG | 83860 |
rs532478491 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8000464 | AATTATGGATAAATC[A/C]AAAGGAGAAAAAAGG | 83860 |
rs532485732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903302 | AATGAGAGGCCCCTA[C/T]AGGTGACCCCTGTGT | 83860 |
rs532491214 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016216 | TGCTGGATCTGTTGG[A/G]TGCTAGAATATGGGC | 83860 |
rs532496236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866391 | GATGGTGGCTGACCA[C/T]GGAATTTCAGGGCAG | 83860 |
rs532523226 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7909171 | GCAGTATCAGCCTCA[A/G]CTGGAGCTTGTCATA | 83860 |
rs532532798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820525 | TTTGAGACAGGGTCT[C/G]ACTCTGTCGCCGAGC | 83860 |
rs532533747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880822 | TTGATGATGCGTGCA[A/G]CAGATGTATATTTAA | 83860 |
rs532536841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872603 | TAATGTGCCATAGTT[A/C]TAATATCTTGCTTTC | 83860 |
rs532538242 | snp | C/T | 1.6623e-05 | 0.00288292 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964314 | AGAAACAAAGTCATT[C/T]ACACCTAAAACAAAG | 83860 |
rs532551958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956809 | TGAAGTATAGCATTC[A/G]CATTTTAGTGACTGT | 83860 |
rs532552243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937784 | GCCCTGTGCTCAGCA[C/G]TCTTACATGCTTTAA | 83860 |
rs532565602 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983672 | AGGTATTTTGCCTAC[A/G]TTAAAAGCTAAACAT | 83860 |
rs532567908 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016767 | ATAACTTTCCCCCCA[A/G]TCTTACTGTCTGAGA | 83860 |
rs532572851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987145 | TGGGCAACGTGACAA[A/G]ATCCTGTCTCTACAA | 83860 |
rs532580094 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823144 | CCAAACTTTTATGAT[C/G]TAAGCCTTCTTTGTA | 83860 |
rs532597745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873304 | TGTTTCTCTCTAACA[A/G]ACCTATTTTAAAAGG | 83860 |
rs532604450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970975 | TAAACCCAATAAAGG[A/G]GAGGGAAATGTTTCC | 83860 |
rs532615653 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868740 | ATCCTAGTGCCATGT[C/G]TTTTGGCACCTAGAA | 83860 |
rs532634499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7854457 | TCTTAAGAAGTTAAC[A/G]TGCTAAAGAGACAAA | 83860 |
rs532635079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995446 | TAGGTTGCCATTTTG[A/G]TTTCCTTTTTATTAT | 83860 |
rs532657194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7915002 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTTACT | 83860 |
rs532658349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7874120 | AGCTGTGAGCTTGTC[A/G]TATAAAATATACCTC | 83860 |
rs532665675 | in-del | -/TAT | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8002338 | GCACATCGTAAAGCA[-/TAT]TATTATGCTTTTTGG | 83860 |
rs532668384 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843008 | TTCTGACATGCTTTG[C/T]ACCTGCTAGGGCGTA | 83860 |
rs532668478 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867040 | GAGGCAGGCGGATCA[C/T]CTGAGGTCAGGAGTC | 83860 |
rs532669877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8002546 | TTGAGGAACTACTGA[C/T]AGAGCAGGGGTAACA | 83860 |
rs532681038 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886212 | GGGTTTACAGGTGTA[A/T]GACACCACACCTGGC | 83860 |
rs532687937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908615 | CTTCTGAAGGAAAGT[A/G]GCACAGAGCTTTATC | 83860 |
rs532691234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865824 | CTCCCGTCACCTCCC[A/C]TATCCATTTCCTTCC | 83860 |
rs532697097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846547 | GTTTTAACTATTACA[A/G]TTTTGAGTGGTTTTG | 83860 |
rs532725618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995941 | ATTTGGTGTTTTTTG[A/T]TCCAATCTGAAATAT | 83860 |
rs532750060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833884 | GGATGAGTTTGGAGC[A/G]GTACCCCTTCAGCCG | 83860 |
rs532752151 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7922725 | GTTTCATAACTAACT[G/T]CCAGTTTTACATACT | 83860 |
rs532754652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912320 | GCCCAAGCTGGTCTC[A/G]AAATCCTGGGCTCAA | 83860 |
rs532756856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7904939 | TCCTCCACACTGAGC[C/T]CTCCATTGCCCTGCA | 83860 |
rs532765321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004937 | TTTATTGTATTCTCT[G/T]TGCTTCTTAGGCTAT | 83860 |
rs532771631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823745 | GTTTGAGCAGTTCTC[C/T]TGCCTCAGTCCCCTG | 83860 |
rs532816865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923593 | ATAGCAAAAAAACAA[A/C]ACAAAACAAAACAAA | 83860 |
rs532835463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950937 | CCTCATAGAGAAAAT[A/G]CATGTGTTACATAAG | 83860 |
rs532838737 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937225 | TTGCTGGATCCTATG[G/T]TAAGAGTATGTTTAG | 83860 |
rs532843007 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7862353 | GTGGATTCTGCTGTT[C/T]TCCTGATGTTTGTTT | 83860 |
rs532850730 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963754 | CAGGGCACATGTATA[C/T]CTGTGTAACAAACCT | 83860 |
rs532874958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827557 | GAGGCGGAGACGGGC[A/G]GATCACGAGGTCAGG | 83860 |
rs532895404 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943346 | GTTTGTTTCCTAGTT[C/G]GTAAGTTTTTCCTGG | 83860 |
rs532902004 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961996 | CTGGGACTACAGGCA[A/C]GCACCACAACACCCA | 83860 |
rs532927399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7884098 | CCCAGTCACTTGTCA[A/G]CTGCCCCGCCTCTCA | 83860 |
rs533006021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891269 | GCCTTCATCTTTTAT[A/T]GATTTATTTGCTTTT | 83860 |
rs533011687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966524 | GCTTTTCAGTCTGTG[A/G]TTTCTTGGATTACAG | 83860 |
rs533044032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857402 | CTTAAACAGTCTGTC[C/T]GGGAGAAAGTTCTCT | 83860 |
rs533045719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926187 | GGTGTTTTTTGAATG[A/T]CCTAAATAATCGTAT | 83860 |
rs533061815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899228 | TCCCTCGATCTGGAG[C/T]CGTTCTCATTCGGTC | 83860 |
rs533070135 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841514 | TGCTTACAGGAATAA[A/G]GGAATCAATGGATAT | 83860 |
rs533076200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974091 | CAAGAACGTGCCACT[A/G]ATCTCCAGCCTGGGC | 83860 |
rs533101387 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7940908 | AGGCTGCAGTGAGCT[A/G]TGATCACACCACTGC | 83860 |
rs533119627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927561 | GTAGATAACGTGGAA[C/T]CAGAATATTTTATGA | 83860 |
rs533151322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7831787 | CTGGTATATCAAAAT[A/G]TTCTAGACTCAGCAT | 83860 |
rs533154134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7836140 | TCACCTACTATGTTT[C/T]TCACGTTACTTAGTT | 83860 |
rs533166245 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7947543 | GCAGTGATCAGAGAC[A/G]GCTTCACTGAGGGGT | 83860 |
rs533181843 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7935023 | GGCTCATGCCTGTAA[C/T]GCCAGCACTTCTGGA | 83860 |
rs533189953 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865242 | GGAGGCCGAGGCGGG[C/T]GGATCATGAGGTCAG | 83860 |
rs533203831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999130 | AAGAACAGAGGAAAT[A/G]GTCTTGTATTTTAAA | 83860 |
rs533211583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824720 | AACCAACAAACTTGC[A/G]ACTGACATTACCAAG | 83860 |
rs533211656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832512 | CAGACTAAATTGGAT[A/G]TTTACCACCTGAAGC | 83860 |
rs533218291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918174 | TTACTAATGAAATGC[A/G]TAAAACAAGAAACAG | 83860 |
rs533232530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920291 | AAAAATTAAAAAATT[C/T]AAACATACGTGTGTG | 83860 |
rs533240608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934547 | CTTTCCAAGTTCAAG[C/T]GATTCTCCTGCCTCA | 83860 |
rs533253945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869203 | AGATAAAAGAAAGAT[A/G]TCACATATAATCCCA | 83860 |
rs533256198 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914382 | CCCCCTCCTATTTCA[A/G]TCATTTCACTCTGTT | 83860 |
rs533258641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871563 | ATTCTGCTGCCTCAG[C/T]CTCACAAGTAGCTGG | 83860 |
rs533267701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906706 | ACGAATTAAATAGAG[C/T]GCAAGCAGCATGTAA | 83860 |
rs533268365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825448 | TCCAGAACTTTTGTT[C/T]CCTCCCAAATTGAAA | 83860 |
rs533269685 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949027 | GTGCCCGGCTGCTGC[C/T]GCCGCTGCTGACAGC | 83860 |
rs533270060 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918012 | GGAAGGTAGCTGGGC[C/T]GGGGCATTTGTTAGT | 83860 |
rs533292322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913706 | TACATCAACCCATTG[A/T]TGAATCTTGACATCA | 83860 |
rs533307743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953214 | TCACTTCAAAAAGTA[A/G]GGTAGAGTTGTTCAT | 83860 |
rs533351635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7975574 | CCTGGATGTATGGTG[C/G]AATAACTAAGAGGTA | 83860 |
rs533354942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962296 | TAGCTCTGACCCTTA[C/G]TGCCTCTCACATCAC | 83860 |
rs533388793 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884526 | CGAGTAGCTAGGATT[A/T]TAGGCGCCCGCCACC | 83860 |
rs533391179 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7870702 | AGTTCGCCTTCCTTC[A/T]CTTCTTCTCTAAGTC | 83860 |
rs533391913 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7840138 | AAGTAATTCTATGAA[G/T]TATCTTAGGAAAATG | 83860 |
rs533410849 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7961667 | TCTTTCTCTCATGCA[C/G]TCTGTCCTGTTTTCT | 83860 |
rs533425547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983294 | AAGTGGTAGGTTCCA[C/G]AAGGAAAGGAGGGCT | 83860 |
rs533429398 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968113 | CTACAAATCTACAGA[A/G]GTAAGGCACCAAAGG | 83860 |
rs533446953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928207 | CTCTTACTGTTTTGT[A/G]TATTCCACTAAAATA | 83860 |
rs533463811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864417 | ATGCATTGTGTCACA[C/T]AGTTAACTCTTTGTG | 83860 |
rs533468753 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879580 | ATATGGACTCCTGAA[A/G]TACAAAGTGTAAACA | 83860 |
rs533512569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999254 | GCTGTGTTTAATACT[G/T]CAAGTAATCCAAAGA | 83860 |
rs533532895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7891153 | TGCAGGTTTTTGATA[C/T]AGGTTATCTCCCATT | 83860 |
rs533550755 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817437 | TGGAATAGTCCCTGT[C/T]GGAGGAATATAGAGC | 83860 |
rs533589130 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8014426 | GAGAGGATGAATGAA[C/T]GGATGAGTCTCTGCA | 83860 |
rs533592246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891883 | TGTTTGTGGAACATT[A/G]CCAATATAAATGGAG | 83860 |
rs533600155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014075 | GCTTATCTATCCTTC[G/T]TATTAAAAATAATAA | 83860 |
rs533624839 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887712 | CAAGAAAAGGCTTCA[A/T]TCCAAGCTAAAATCG | 83860 |
rs533634445 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7997544 | TCTATTTATGTCACT[C/G]GTTTGTGGTGGGGAA | 83860 |
rs533647616 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7837396 | GCCTGTAATTTCAGC[A/C]CTTTGAGAGGTTGAG | 83860 |
rs533658199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013470 | GATGATTATAAAATG[C/T]TTTTTATGACTTACA | 83860 |
rs533669198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7963476 | GCCACTCTTTTAAGA[A/G]TGATGGCACACATGT | 83860 |
rs533673051 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7885644 | CAATTATCCATGTTT[C/T]TAATTCAAATGCTTC | 83860 |
rs533708053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968199 | ACCAAAGGTTAAACT[A/G]AAGTGAGACAAGCTG | 83860 |
rs533733162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7904500 | GCCTGATACACGCAT[G/T]TATCTCATATTTGTT | 83860 |
rs533744998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7911746 | AAATTTTACGTAACA[A/G]ATAAGCAGTGTTTAC | 83860 |
rs533748086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990112 | TGGCTAATGTTTGAT[A/T]TTAGCCTGGTTTTGA | 83860 |
rs533766886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863247 | CTGCAGGGTTTTGTA[C/G]TGGGACTGCATGGAA | 83860 |
rs533767200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934593 | GGGATTACAAGCACC[C/T]GCCACCACGCCTGGC | 83860 |
rs533787197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982857 | GGCATTTTTTGTTGA[A/C]TTTTGCACACTTTCC | 83860 |
rs533790993 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821209 | GGTTCATTATTCCCA[A/C]GTAATTTGGTGACTT | 83860 |
rs533802877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905084 | CCAAGTAGTAGGAGG[C/G]CATTTTCTTTGAGAA | 83860 |
rs533815617 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923637 | CAACAGTTGCTTTGG[C/T]TTTCATCCTGTATTC | 83860 |
rs533824251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856834 | ACTCACTGGTGCTCT[A/G]GTAAATGTTTAACAG | 83860 |
rs533828420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941061 | TGCTGCTGGAAGGAA[G/T]AAAAGTCAAGGAAGA | 83860 |
rs533843597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946436 | ATTCTATTTAAGAAG[A/G]TGGTGGGCCAGGCAC | 83860 |
rs533849380 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7836532 | GCCCACCTTGGCCTC[A/C]CAAAGTGCTGGGATT | 83860 |
rs533851206 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7820573 | GATCTTAGCTCTCTA[-/T]AGCCTCGAACTTCAG | 83860 |
rs533852233 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865427 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCTCTG | 83860 |
rs533854904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898660 | TCTGAAGCTCTTCAA[A/G]CACTGGGTTCTTATA | 83860 |
rs533861991 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7978418 | GAGGCAACTTGGTTT[G/T]CCAGGGGAGTGTATA | 83860 |
rs533867145 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990117 | AATGTTTGATATTAG[C/T]CTGGTTTTGAATATA | 83860 |
rs533898323 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957842 | CGATGTTGGAACACA[A/G]CTATTATTATTATTA | 83860 |
rs533910485 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927466 | TCCCAGCTCTGCCTC[C/T]CTTTTGTTCCCTCCA | 83860 |
rs533932020 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818141 | TTTTTAGCTGAGGCA[A/C]CACCAGCGCAGGTCT | 83860 |
rs533955205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013647 | TATTCGGTTAACAGT[A/G]TAAAGTAATCATTCT | 83860 |
rs533956461 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7858622 | TCAGTCTTTTTGTGT[A/G]TTCTGCCTGTCAATA | 83860 |
rs533960067 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7975232 | GTTTGTAGGGAATTG[A/C]CAGAGCTCTCCTTCA | 83860 |
rs533963643 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838261 | GAGATGAGTGAGATA[G/T]TCCTCTCTCCCCATT | 83860 |
rs533975292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823256 | ACTGTTTAAGATTCT[A/G]CAGATGCATCAGGGA | 83860 |
rs534006844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856395 | CGAGGCAGGAGAATC[A/G]CTTGAACCCAGTAGG | 83860 |
rs534010508 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7945059 | TTTACTCTATTTTCA[-/T]TTTTTTTTGGTAGTA | 83860 |
rs534016957 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7851649 | CCCTTCTCCCCTTTC[A/G]TGTTGGCTTGATGAA | 83860 |
rs534023392 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963227 | ATAATAATCCATACT[A/T]AGTCCTATAATAATC | 83860 |
rs534025736 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7974560 | AGAGGAGAGGGCCAA[A/G]TAAGGTTGGGTGAAA | 83860 |
rs534027245 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836554 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 83860 |
rs534044139 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816802 | AACCAAGCCTGTGAC[A/G]TATGGTCTTGTGTAT | 83860 |
rs534077099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934078 | CGATAGCGTAGAGAT[A/T]GATACTGTGAGGCAA | 83860 |
rs534100921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7992592 | TTTAGAAATGGAGAA[A/G]TGTGAAGAAAAAAAT | 83860 |
rs534105035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878054 | ACCATGTGCCTCTGG[C/T]GTGCAAAATAATAGG | 83860 |
rs534131845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941826 | GAGAGCCTGGAGCAT[A/G]TGTGTCAGCAACAGA | 83860 |
rs534135600 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009936 | TTTTTTTTTGAAAGG[A/G]GATTTCACTCTGTCA | 83860 |
rs534135669 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8006507 | ATATTCATCGGTTAT[A/G]ATGTTAAGCATTTAT | 83860 |
rs534143587 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7940304 | AAACTACCAGATGAT[G/T]CAGTCTCAATTTAAT | 83860 |
rs534188594 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011641 | ATCATCAAATTGGTC[C/T]ATTCGGGGACCAATC | 83860 |
rs534191323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7919566 | GGTGGTCCCTCATAA[C/T]CATGGAGCATTGGTT | 83860 |
rs534193110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948406 | CGTCTGATTTTAAGA[A/G]TGTTTATTCTGTATA | 83860 |
rs534196696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824123 | TAGTTGTCTGATTAT[A/G]TTTAAACTTGACTTT | 83860 |
rs534205272 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982681 | CTGGGATTACAGGTG[C/T]GAGCAATCTTGCTTG | 83860 |
rs534256715 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7824807 | CAAGTAGAGGAAAAC[A/C]GTGAAGCCAAAGAGA | 83860 |
rs534258645 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817505 | ACTAAATACACTGTG[A/G]TAAGTACAGAAGGGC | 83860 |
rs534262082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7954725 | TTCAGAGTGCACTCC[A/G]TAGGTGAATGAGTGG | 83860 |
rs534274728 | in-del | -/T/TT | 0.627431 | 0.0981961 | intron-variant | TAF3 | GRCh38.p7 | 10:7843646 | ATCTCTTTCTCACTC[-/T/TT]TTTTTTTTTTTTTGA | 83860 |
rs534277283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012691 | CCACAGATTTCTTTA[A/G]GAAGTTTTCCTGTCA | 83860 |
rs534278379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860942 | TAGCTGGGATTACAG[A/G]CACCCACCACCATGC | 83860 |
rs534278921 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7859086 | GCTAACACGGTGAAA[C/T]CCCGTCTCTACTAAA | 83860 |
rs534308741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900594 | ATAATGTGGGGCATG[A/G]AATCGAATCTCAACT | 83860 |
rs534310815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975852 | TTCAATTATGATGTA[A/C]TTCATGAGCTTGAAA | 83860 |
rs534310960 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7967710 | ATACAAGGTGTGCTT[A/G]GTACCGTATCTGACG | 83860 |
rs534315791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7957147 | ACATCACTTTTGGGA[A/C]TAATCCTTACTATGC | 83860 |
rs534345222 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852318 | TCAAATGTTATAAAC[A/G/T]TTTGTTGGTTTATTA | 83860 |
rs534361085 | in-del | -/ACACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939612 | CACACACACACACAC[-/ACACACACAC]CTCTACCTACACCCC | 83860 |
rs534397100 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016459 | AATTTTTCTATCCCC[A/G]CTAAGAAACAAAGCA | 83860 |
rs534429226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870181 | AGGTTTAACTTTGAA[C/T]TCATTCTTATGAGTA | 83860 |
rs534435763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991760 | AAGAATTCATATAAA[G/T]CATGGTGATTTTGGT | 83860 |
rs534436482 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7832222 | TGCCCCAGCCTCTGT[-/A]AACCACTGTTCTACT | 83860 |
rs534437918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878631 | CTGTAAGTGAGAAAC[C/T]CAGAGGCCACTAGCT | 83860 |
rs534448923 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953840 | GACTCAAGAGTGCAC[A/G/T]CCATAGGCAAATGAG | 83860 |
rs534480869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955317 | AGTTTGTGCATCATT[G/T]TAGAAATTAATTTCT | 83860 |
rs534485372 | in-del | -/T | 0.368529 | 0.220116 | intron-variant | TAF3 | GRCh38.p7 | 10:7873624 | CGAGTTCTCCCCCCC[-/T]CCCCCGTCAAAAGGG | 83860 |
rs534486750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000102 | CGTATACATTGTAAC[A/G]GGCATTTTCATCTTT | 83860 |
rs534487684 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856340 | AATTAGCCAGGAGTG[A/G]TGGTGCGTGTGTACC | 83860 |
rs534492598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870868 | AATGTATTCTAAGCC[C/T]TACCTTTCTTGAAGC | 83860 |
rs534495763 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842163 | ATTGTTTTTTTTTTT[-/TG]TTTTTTTTTTTGTTT | 83860 |
rs534512287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951640 | CTGTAGAAGCCCAGT[G/T]GAAGGGCATAGATGC | 83860 |
rs534567166 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7866910 | TCCAAATTTAAAAGA[G/T]AAATTTTAGATCAAT | 83860 |
rs534577250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923769 | TACAAATATTGCTAT[A/C]GTTGATCATCCATTG | 83860 |
rs534577269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951203 | GTGACAGTATGTGTA[C/T]ATATGAATACATAGC | 83860 |
rs534605620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866222 | ATGTCCACTCTGTGC[C/T]GTCACTCTTCCAGGC | 83860 |
rs534619103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008825 | ATATTTCTGTGAACA[A/G]TGCATGTGTATTGGT | 83860 |
rs534635494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820166 | GCCCGTGGCCCACCA[A/G]TAGTATTACTTTTAT | 83860 |
rs534661478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902894 | TACCCTTTTTTAGTG[G/T]TTAGAATAGACTCAG | 83860 |
rs534666070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7932881 | ACGGGGATCTCAATA[C/T]ATTGCCCAGCCTGGT | 83860 |
rs534675486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981090 | ATTCAGGTAAAGGAG[C/G]TTTGTGAGAAAAAGG | 83860 |
rs534677489 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836055 | TGAGCTCCATCTTGG[G/T]GCCTTTCTTGGGCAC | 83860 |
rs534680806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883563 | AATACTCTGTTTCTC[A/T]TCAAACTTTTACCTA | 83860 |
rs534682969 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873964 | CCCTCGAGAGGCCAT[C/T]GCAGGTTTTAGTCTG | 83860 |
rs534683547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972756 | TGATTCCTTTGTCCT[A/G]CCAAGCCATTTAAGA | 83860 |
rs534689097 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870441 | TCCAGTGGTCGGTTA[A/G]AATATAATTTATTTA | 83860 |
rs534733245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896171 | GTTCTATTGTGTATG[C/G]TAGTAAGGTAAAAAC | 83860 |
rs534748322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988888 | GTGTAAAATGGTACA[C/T]TGTTTGTACTTTGCA | 83860 |
rs534779654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881286 | CTCTTTTAATATACT[A/G]TTTTCCCACCATGTG | 83860 |
rs534786271 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7868489 | GTGGTGTGACATAGC[A/G]GCCAAGTTCTAGTGA | 83860 |
rs534787376 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868188 | GTATTGTTTGACAAG[C/T]GAGATGTTCTGAAAT | 83860 |
rs534829437 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7834071 | GTTGTGGCTCTTGTT[G/T]TTGTTGAGTTGCTTA | 83860 |
rs534845340 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981315 | GTCCCCCATGCCCAG[A/G]TCCATGGTGAGCAGC | 83860 |
rs534847648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881799 | CTTTCAATTTCCTTT[A/G]CTGTGTAACTTTGGA | 83860 |
rs534848626 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7937981 | TTATATTGAGGGCCG[A/C]TTAGAGGGGATTTTG | 83860 |
rs534856969 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:8011689 | AGAGGCAACATCACC[C/T]CCAAATGGGTTGATC | 83860 |
rs534888627 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7888695 | TAAAAGCTTTTGGTC[A/G/T]AATATACTATACTAA | 83860 |
rs534897994 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906779 | ATTTTGTAAAGGAGG[A/G]TCAGTTGAGCCCAGG | 83860 |
rs534899088 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978021 | AATAAGATAATGAAA[C/T]ATTGATTTTTTTTTT | 83860 |
rs534909131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002694 | TTTTTTAAATGTCCA[C/T]AGAGTCAATTTCATT | 83860 |
rs534910014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7847607 | TGTTACCACATCCAG[C/G]TAATTTTTTTTTATT | 83860 |
rs534953360 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001554 | CCTTTTAACTTTGCT[A/G]AGGTTATTTTATGCC | 83860 |
rs534962796 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905411 | AGACAAAACCTTTGT[C/T]TTCATACACGATGAA | 83860 |
rs535013533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890220 | TCTTTTCTGTGCTTG[G/T]AAGGACCATCTCTTC | 83860 |
rs535029099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828764 | ATAGGCTGGGCGCAG[C/T]GGCTCACACCTGTAA | 83860 |
rs535029894 | snp | A/G | 1.79538e-05 | 0.00299609 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965649 | GAAGAAAAAGAAGGA[A/G]AAAGAGAAGGAGAAG | 83860 |
rs535032456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7842010 | TGGATGGTGGGCTTT[C/T]ACCAAATGACTGCCT | 83860 |
rs535035860 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7932153 | AGTATAGTCACTGTT[G/T]TAAAAAGTAAAAGGA | 83860 |
rs535091038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917716 | AAAGCCTAACAAGCA[G/T]TTGTGCTACTGGACT | 83860 |
rs535095867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829601 | AGATCTTGGGGAGAA[A/G]GACCACAGAGGTCAA | 83860 |
rs535098235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938513 | GGGAAGGCTTGAAAA[C/T]TCATGTCTCTAGTTG | 83860 |
rs535116101 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947974 | ACAATTCTATGTTGA[C/T]GCACTATAACTTCCT | 83860 |
rs535119276 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7988219 | ATAATCCCAGCACTG[C/T]GGGAGGATCGCTTGA | 83860 |
rs535128632 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906047 | AGTGTATTGTGTCAG[G/T]ATAATTAAAAGTGCT | 83860 |
rs535136801 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7842183 | TTTTTTTTGTTTTTT[G/T]TTTTTTTTGAGACAG | 83860 |
rs535153370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7911093 | TGATTTTTGAGGGAG[A/G]AGACTCACACCTGAA | 83860 |
rs535158810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904341 | TCTATTTATGCTTTG[C/T]AGCCCTAATACAACT | 83860 |
rs535160805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822549 | GTCTCCTGCTTCCAC[C/T]ACAGCCCTCGCCTCT | 83860 |
rs535177393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856315 | ACCCCGTCTCTACTA[A/G]AAATACAAAAATTAG | 83860 |
rs535212610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897823 | TGCCACCATGCCCGG[C/T]TAACTTTTTGATTTA | 83860 |
rs535238008 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930066 | AGCAAAGTGGGGTGG[C/T]ACACACCTGTGGTCT | 83860 |
rs535278402 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7938546 | TGAGAGAATTTGAAC[A/G]GCCAGTCAGACAAAA | 83860 |
rs535280635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946240 | TTGACCTACCCAACC[C/G]ACCTCCTTTCCTCTT | 83860 |
rs535312624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841318 | TGCAGGCTCACTGCT[C/T]ATTTCTGAAAAGAGA | 83860 |
rs535326298 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7875572 | GGGTTGTTGGCCTCC[A/T]GTTGAAAAGTAGCAT | 83860 |
rs535329838 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828889 | AAATACAAAAATTAG[C/T]TGGGTGTGGTGGTGC | 83860 |
rs535332931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916755 | TATAAATGTGGATGG[C/T]TATATATCTTGTTGC | 83860 |
rs535341615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828406 | ATGTGGAAGGAGTTA[C/T]TGCCTGCTTTATCTG | 83860 |
rs535350258 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849834 | ACAGGCATGCACCAC[C/T]ATGTCTGTCTAATTT | 83860 |
rs535355705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909463 | CCAGAAGCTTCCTTG[A/G]ACTTCACTGTGCCAT | 83860 |
rs535357566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952506 | TGTAGCCATAGAAAC[C/T]CCAAAGTCATATTGT | 83860 |
rs535375911 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7835179 | ATTGTCTTTGGCCAC[A/G]CATAAAATACACTAA | 83860 |
rs535380038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7858989 | ACCTTATTGAAAAGT[A/G]TGGTGGCTCACGCCT | 83860 |
rs535401547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8003630 | ATAAGAAACTATCAT[C/T]TGTTGCATTTAATGC | 83860 |
rs535423011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903774 | GTTTTATTTAGCCCA[C/T]GTTTAAGAAATATGT | 83860 |
rs535425823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958861 | GGCTTTTGGCCGGGC[A/G]CGGTGGCTCACGCCT | 83860 |
rs535432020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7868582 | TTGGATTCACATCCT[A/G]GAGCAGCCTGTTAGT | 83860 |
rs535449883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966395 | ATGTTTGACCATCTC[A/T]GTAAGTCAGACTTCA | 83860 |
rs535457285 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003783 | AGGCACAGTGGCATG[C/T]GCCTGTAATCCCAGC | 83860 |
rs535463101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974343 | AGGGGCGGTTTGTGG[A/G]CAAGTTGATACGTTA | 83860 |
rs535471068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830544 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 83860 |
rs535506154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869347 | ATAAATACATACGTA[C/T]ATAGATGTTGATTTC | 83860 |
rs535510306 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852927 | ACCTTCTTCCAATAG[G/T]CACCAACTAGTTGTG | 83860 |
rs535531226 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7823311 | TTGACTTTGTCAGCA[C/T]AGCACACTACTTATT | 83860 |
rs535543245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863300 | GTTGAGATCTTCACA[A/G]TATTGAATTTTCTGA | 83860 |
rs535564159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972522 | GAGGCATCTGTGTTT[A/G]GATGATACAAACACT | 83860 |
rs535608555 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7880137 | CAGCTACTCAGGAGG[-/CT]CTGAGGTGGGAGAAT | 83860 |
rs535609860 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7983146 | GAGGTGGTCCTGGCC[A/C/G]CTCAGGCTGTTGTGA | 83860 |
rs535623501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845125 | TACACCAGTGTCCCA[C/G]CAGTCTCCCTGGAAT | 83860 |
rs535623933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998667 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 83860 |
rs535634682 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955421 | TCTAGCTTTAAATAC[A/G]TTTAATTTTTGATGA | 83860 |
rs535644281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005664 | CAGGGTTCCTGCTTT[C/T]CCCTTTAGCTTTGGT | 83860 |
rs535682608 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7911140 | CTAGATCTTTTAAAG[-/A]AGGTGCTTTAAGAAA | 83860 |
rs535693631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997051 | TCAAGGTGGTTGGTA[C/T]TTCTGAGATTGATCA | 83860 |
rs535697698 | in-del | -/GTGATGAA | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:7877725 | CAACTGAGACCCATT[-/GTGATGAA]GTGACTTGGCCAAGA | 83860 |
rs535706689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012516 | GGCCTTCTGACTTCA[A/G]GCAAGGTCAGCCAGC | 83860 |
rs535717017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835809 | AGATGCCTCATACTC[A/G]GGTCTCATGGCGCTT | 83860 |
rs535727039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7949892 | GGCAGGCAGTGACTG[C/T]GCATCACCACTGCCT | 83860 |
rs535753420 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882663 | AAAGGTGGAGTGCTC[C/T]TATCAGAAGGCAGTG | 83860 |
rs535757478 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7996468 | TGCCAGTGTGTGAAT[G/T]CCAGGAGGCCAACCA | 83860 |
rs535766381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966746 | TATTACCAATAAATT[C/T]GGAGTATTTTTAACT | 83860 |
rs535769618 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928714 | ATTCTACTCACGATG[A/T]TCTAGGTAATGGCCT | 83860 |
rs535780794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978519 | CCACATTACTCTTTT[C/T]GGTTGTGCCAGTAGA | 83860 |
rs535788536 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831802 | GTTCTAGACTCAGCA[A/T]GTATAGTCATGTTCT | 83860 |
rs535828736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7977564 | CTTTTTTAAAGACTA[C/G]CACCTGACATTATTT | 83860 |
rs535828905 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7969169 | ACAAACAAACAAACA[A/G]AAACCTATTTTTTAA | 83860 |
rs535854777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918295 | AGAGAGAATGATCCA[A/G]GGAAGAGGTGGGATT | 83860 |
rs535859936 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7825713 | CAGAATAATATATGT[A/G]CATTCCACATTTGTT | 83860 |
rs535868348 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7931977 | GCTAGAGATACGCAA[-/C]CAGAATATATTTTCC | 83860 |
rs535879112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872668 | CTTGCAGGGTTTTCA[A/G]AACTATATCTGCATT | 83860 |
rs535889373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976640 | GAATTCCTGACCTCA[C/T]GACGCCTGCCTCAGG | 83860 |
rs535919067 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7911906 | CTTGCTTTACTCGTT[C/T]GCTTCATTTTTCTGG | 83860 |
rs535932727 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7865550 | GCCTAGAAACCTTGG[G/T]GCGTGCTGAGCTGTG | 83860 |
rs535947978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935846 | TGAACGAGGGAGAGG[A/G]AGATAAAAATGGCCT | 83860 |
rs535962485 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816888 | GTTAAGTGTCATGAA[C/G/T]TTTGCAGCTTATTTT | 83860 |
rs535962900 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8001126 | TGCTACAAATCATAT[C/T]CTTTACCCCAGACCT | 83860 |
rs535969848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7984529 | GCTAGTAAATCTAGC[C/T]TATCTTGAGTCCAGA | 83860 |
rs535975449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905193 | TGAAATACACCCTAC[A/G]TTAGAGTTTGAGACC | 83860 |
rs535982717 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7912483 | TTTTTTTTCTGGGAA[C/G]AGTCATGAGACTAAC | 83860 |
rs535987122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942327 | TATCAAACATATTTT[A/G]AGCCATCTGCTTTAA | 83860 |
rs535992188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908096 | TATTCCACATTTCCA[A/G]CCTGCTTTCATTCCA | 83860 |
rs536034644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7963654 | TCACACATCGGCACC[C/T]GTTGGGAGGTCGGGG | 83860 |
rs536035187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890331 | CCTAATTGGATGCTC[G/T]TGGTATAGCCCTTTA | 83860 |
rs536042686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845168 | TGTATTGTTTTTTTA[C/G]TAGCTTAGATTAAAC | 83860 |
rs536084887 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7883594 | CTAGTTTATCATCCA[C/T]TGGTGATCTTTACTC | 83860 |
rs536090698 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921230 | TACTTTGAAGTAGAA[A/G]GAAAGAGCAGTTTTA | 83860 |
rs536092724 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962208 | CTTATACCCTAATCA[C/T]TTATCAGATTCTATC | 83860 |
rs536106057 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7838795 | AGGATCTGGCTGCCT[C/G]TCTCTTGGCCCTCTC | 83860 |
rs536114519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963208 | CCTGTCATTCCTGAT[A/G]ATAATAATAATCCAT | 83860 |
rs536146767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876420 | GAAATGGGCCATAAG[C/T]AGGTATTTTAAAGTA | 83860 |
rs536153390 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015010 | CCCTCCTCCACTTCT[C/G]TAATACCAGTGACAA | 83860 |
rs536162714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969951 | AGACAGCAGCATTCT[A/G]AAGTTTAACTTATCT | 83860 |
rs536168652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7839240 | CTGGCTTCTTTGAGC[A/G]CCCGTATAATATATA | 83860 |
rs536195181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917738 | TACTGGACTAGATAC[A/G]GGGTGCGAGGAGAAG | 83860 |
rs536202473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929248 | GAGAGAAGTAGTTTA[C/T]TTTTTTTGTTGTTTT | 83860 |
rs536204293 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947494 | CAATGAGGCCAGGTA[A/G]GAAAGCTACTGGGAG | 83860 |
rs536212144 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7995532 | TACCTGAATATTAAT[A/G]CCCTTTTAGAGATTT | 83860 |
rs536213556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7974841 | AGCACTTTGGGAGGT[C/T]GAGGCGGGCGGATCA | 83860 |
rs536216869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880231 | TGACAGAGTGAAACC[C/T]TGTCTCGGAAAAAAT | 83860 |
rs536221220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986578 | AAAGTTTCCCAAGCT[A/G]AACAAAACCAAGGAA | 83860 |
rs536231148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888053 | TTAGGTTCCCTTGCT[C/G]TGCAGCCAGCCGTCA | 83860 |
rs536234669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833469 | TGAACATTTTTTCAT[A/G]TATTTGTTGGCAGTT | 83860 |
rs536258363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922229 | CTCATTGAATAAGCA[A/G]ACTATCACTGCACTA | 83860 |
rs536272487 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000632 | CGTATACAAAAAATT[A/G]GCCAGGCATGGTGGC | 83860 |
rs536291993 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892064 | CAAAACCCAGATGTT[C/T]AATTATTCATTTATT | 83860 |
rs536296107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7826181 | GGTGGCTCATCATTT[A/G]GGTGCTCTGGATCTT | 83860 |
rs536298437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881401 | CGCCTCCAAGTCAGC[A/G]GTATACGAAAACTTC | 83860 |
rs536366447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819590 | TTATGAGTTTTAAAT[C/G]AATGTCTGGTAATAT | 83860 |
rs536382929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915097 | AGGTGCCTGCCACCA[C/T]GCCCAGCTACTTTTT | 83860 |
rs536384916 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998966 | ATGTAAAACCATTTC[C/T]GGAAAACAGAACAAA | 83860 |
rs536388720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923873 | TCTTAAGAAATTTGT[A/G]TAAAGCTAACATTTG | 83860 |
rs536391376 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967788 | TAAAATGTAGGAACC[G/T]GGAGATTGCTGCTCC | 83860 |
rs536397756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860343 | GCGTTTGAAAATTAG[C/T]TTTTATAAATGGTTG | 83860 |
rs536401187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865876 | CCGTTTTATGTCTCT[C/T]GCATCTTGTCAGCGT | 83860 |
rs536414833 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926115 | AGATCTCTGATCTTT[A/G]AAAAAATTAACTTTT | 83860 |
rs536416187 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870635 | AAACTTCTACAGACT[C/G]CTGACTTGAGTTTTT | 83860 |
rs536419057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008728 | AGGCCCCCCCGAGGA[C/T]TCAGCAGAGGTGGGG | 83860 |
rs536438415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901542 | AAACAGTATTATGTG[G/T]GGCTGTTTAGATGGC | 83860 |
rs536528216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7930077 | GTGGCACACACCTGT[C/G]GTCTCAGCTACTTAG | 83860 |
rs536593152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920867 | TTAACAGTGATTTAT[A/G]CTGTAGCTAAAAAGC | 83860 |
rs536617367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917722 | TAACAAGCAGTTGTG[C/G]TACTGGACTAGATAC | 83860 |
rs536634985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819655 | GAATGGAATATTTTA[A/G]TAGAAGCTCCACATT | 83860 |
rs536653119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7846596 | CATTTCATGATTTTT[A/G]TTCTTTCCTAGAGGC | 83860 |
rs536706388 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849675 | GGGGTTCATGCGAAC[-/T]TTTTTTTTTTTTTCT | 83860 |
rs536707035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840659 | ATATCAAGGAGGAGC[A/C]GGCAATACATGCTTG | 83860 |
rs536724626 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915433 | GTGGATCACGAGGTC[A/C/G]GGAGATCGAGACCAT | 83860 |
rs536734479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929357 | TGTGAAGTAAGATAC[A/G]TACAAGGAAGTAGTA | 83860 |
rs536749506 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969892 | TCCTCGCAGACCCTC[C/T]GCTTCCTTCCTCCGT | 83860 |
rs536762632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7977742 | TTTTTGCTCAGATGG[C/T]ACATGGTTTTATTCT | 83860 |
rs536774166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902329 | TCGGGAGGCTGAGGC[A/G]GGAGAATCACTTGAA | 83860 |
rs536776986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834586 | GATAGGTGGATAGGG[C/T]TCCTCCTGAGTTCAT | 83860 |
rs536797868 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941588 | CCCTCTGCTTCGCCA[C/G]TGCCTCACTGTATCC | 83860 |
rs536811792 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7872339 | TCCCTGTATAATTAG[C/T]AATGGAGCCTTATTC | 83860 |
rs536825720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994991 | AGAAAAAAAAAAAAA[A/G]AAAAGAAAAAAGAAA | 83860 |
rs536845275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908723 | TTTCAAGCCACAAAA[C/T]CCTTTCTTCAACAAA | 83860 |
rs536852398 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7839262 | TAATATATATCTCTA[C/T]CATCATACTTCATAT | 83860 |
rs536852438 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7957619 | CTTACAACTAACAAT[A/C]AATTTTTTAAATTTT | 83860 |
rs536855017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950510 | TTTAGTTCATGAAGC[A/G]TATTTATTCTTTTCA | 83860 |
rs536867339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7860831 | TTGAAATAGAGTCTC[A/G]CTCTGTCACCCAGGC | 83860 |
rs536871437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931010 | AGAAGAACTTAATTT[G/T]ACTCTACAGTACCAG | 83860 |
rs536878603 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7846147 | GTGTTTTGGTAGAGA[C/T]GGGGTTTCACCGTGT | 83860 |
rs536910498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902259 | AGAAACCCTGTCTCT[A/C]CTAAAAATACAAAAT | 83860 |
rs536914008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833527 | TTCATTTTTTATTGG[A/T]TTATTTCTTTCTGTA | 83860 |
rs536930090 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836040 | ACTCTCCTTATATGA[A/T]GAGCTCCATCTTGGG | 83860 |
rs536931711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7853936 | CATCTGTGAGAATCA[A/G]TTGGCTGCATGGAAT | 83860 |
rs536943846 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868095 | TGGTCTTGCTGTCTC[A/G]GGGGTGGCAGAGGTG | 83860 |
rs536945325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8008775 | CTGAAGCCGTCAGAG[C/T]TTCTGCCCCAGCACA | 83860 |
rs536950737 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893568 | TGTGGCTTTTGTTGC[C/T]GTAGCTAGTTGCTCC | 83860 |
rs536958320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987218 | TCCCACGTACTCAGG[A/T]GGCTGAGGCTTCACT | 83860 |
rs536986979 | in-del | -/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850695 | AAAAAAATATATATG[-/TA]TATATATATATACAC | 83860 |
rs536989317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846158 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGACG | 83860 |
rs537003715 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016423 | ACAGGGTGTCATTGC[C/T]CTCGTTGTTCAAGAG | 83860 |
rs537031604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889380 | GTAAACACTTCACAT[A/C]TACTCATTTAATCTT | 83860 |
rs537034204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987982 | CAGAGAATTGCCTTC[G/T]CTGTGATAGTGTTTG | 83860 |
rs537041492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970680 | TTTAAAGAGCAGGAA[A/G]GGGATATCCTTTACA | 83860 |
rs537043728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7827085 | GTTCATGTCAAAAAA[A/G]CCTGTGAAAGTCTCC | 83860 |
rs537057315 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950342 | GGGCATGAAGACCCT[C/G]TGGAGGGAAAGACCT | 83860 |
rs537058648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841207 | GCTTCTTTTACGGTG[C/G]TTATATACTGATGGT | 83860 |
rs537062375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923976 | TTGTACTTGAATTTT[A/T]AAAAATTTGATAGAA | 83860 |
rs537065553 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015337 | AATACCTTATATTTT[C/T]TAAGAAAAAGGTTTC | 83860 |
rs537084609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866104 | AGTTTTTTCTGGATC[G/T]TAAAGTAATTTCTGA | 83860 |
rs537089420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882842 | AGAATAGCACAAAGA[A/T]TTCCTAAGTATTCTT | 83860 |
rs537094384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987309 | CAATAGGAGTGAGAA[A/C]CTGTCTCAAAAAAAA | 83860 |
rs537169146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909267 | TCTGAGAGGGCTCTA[G/T]TTGATTCTTGTACAT | 83860 |
rs537171913 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891618 | CTTTACCTTCTTATG[G/T]TTTTGTTAGAAACTT | 83860 |
rs537176983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002894 | AATTTTAAACTGTTA[C/T]AGCTTCCTGGCAAAT | 83860 |
rs537210919 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:8008715 | GCAGCCCCTGTCAGG[-/C]CCCCCCCGAGGACTC | 83860 |
rs537214248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904901 | GAACCCCAATTCCCC[A/G]CACTTCCTCCACCAC | 83860 |
rs537224914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002644 | CAGTATATTTTAGAA[A/G]AGAATGAATATTCCG | 83860 |
rs537239924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895566 | TAAGACTTTTGGTCA[C/T]AAGTATAAGAGTCTT | 83860 |
rs537269934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854657 | AAAGAGCCCTCTAAT[G/T]GGGGGGCGGGGGGAG | 83860 |
rs537282658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7880414 | AGGTGGTAGTCTGGA[A/G]GGAATTGGTGGATGT | 83860 |
rs537317603 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928606 | TGTAGGATTGCCCTT[C/G]TGTTAATAACCATGA | 83860 |
rs537346360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881260 | AAAAAAACAAAAAAA[A/C]AACCCACAAGCTCTT | 83860 |
rs537366601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888620 | TGCCCAGTTAGGTGC[A/G]TTTACAGGTTATGTA | 83860 |
rs537381575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914651 | CTTTTACTGTAAATT[A/G]TTAATAAAATCTATT | 83860 |
rs537393786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938390 | AATGTGATGGGCGGG[C/G]CTCGCCTAAGGTAGC | 83860 |
rs537395410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931310 | ACTGCTGATCAATGG[C/T]AAACTTGGTCCTTGA | 83860 |
rs537424271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885253 | ATATAAATTTTGACA[C/G]ACACACACACACACA | 83860 |
rs537455850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7937951 | TCAGTGGAACATCCT[A/G]CTTGGAAATGGGGTT | 83860 |
rs537488643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885991 | TGGTGTGTAGTGGCG[C/T]GACGATGGCTCACTA | 83860 |
rs537513563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835128 | ACACAGGTGTCCAAT[C/T]TTTTGGCTTCCCTGG | 83860 |
rs537528846 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893753 | GCCCTTCCTTCTTCA[A/G]CTTTTCACCTCTGTT | 83860 |
rs537530910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944669 | AAGGGTTATCTCTTA[A/G]CTAATCCTCAAGTAA | 83860 |
rs537536302 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865647 | GGTGGATGCAGCCAC[A/G]TGCAAAGTAGCAACT | 83860 |
rs537550334 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890472 | AAAAGAAGTTTAAGC[A/G]TGCAATTGTTTAAAG | 83860 |
rs537553367 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870865 | AAGAATGTATTCTAA[C/G]CCTTACCTTTCTTGA | 83860 |
rs537574545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828527 | GTGTGTTTTATCCAA[A/G]AACATTCTCTCCCCA | 83860 |
rs537583250 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7919743 | GTCTTTATACTGTTT[G/T]TATTGCTATTATTTT | 83860 |
rs537587908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916916 | AATGTAATTGGGTTC[A/G]TACTCAATTATTTTC | 83860 |
rs537589788 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918158 | GTAGTTCTGGTTGTT[C/T]TTACTAATGAAATGC | 83860 |
rs537591708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951118 | ATAGGAACCTAACCG[G/T]GTATTTCTCTTAAGA | 83860 |
rs537600674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863819 | TTCTCAGTGATGTTT[C/T]ATAGTTTTCAGTGCA | 83860 |
rs537602179 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948663 | TTTTACAGGCTGCCT[C/T]CTAAATAGGAAGATG | 83860 |
rs537606725 | snp | A/G | 1.65616e-05 | 0.00287759 | missense | TAF3 | GRCh38.p7 | 10:8013780 | GCCCTGGGTGTAACA[A/G]GCCTGACGATGGGAG | 83860 |
rs537638320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905666 | GCGGGCAGATTACGA[G/T]GTCAGGAGTTCGAGA | 83860 |
rs537640722 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7902821 | GTTGATTTTCTATCA[C/T]TTCTGTATTGAAATT | 83860 |
rs537700173 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823776 | AGTAGCTGGGATTAC[A/G]GGCCTGCGCCACCAC | 83860 |
rs537702746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972620 | CTGAATACCTGTTGC[C/T]TTCCGGGCACATTTA | 83860 |
rs537704351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976060 | TTAGCTTGTTAATTC[A/G]AAATGTTGATTATAT | 83860 |
rs537704491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899407 | TTCCCAGGGACCTGG[C/T]GCCTCTGATCCCCAG | 83860 |
rs537727923 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873594 | GGTGTTATGGATGTC[C/G]CCAAGGGAAGACATC | 83860 |
rs537728103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850449 | GGGAGGCTGAGGTGG[A/C]CAGACCACTTGAGGT | 83860 |
rs537735321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846741 | GGGATCATATTTCCT[A/G]CATCTTGAAACATTT | 83860 |
rs537751809 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899286 | CCCTTCCCCAGATGT[C/G]TTCTGCCCAAGGGAA | 83860 |
rs537761770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7892022 | TTTCATTAACAGATA[A/G]ATTTTCTTCTTTTAA | 83860 |
rs537771049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983575 | GATTTAAAAACAACA[A/G]CAACAACACAAAAAA | 83860 |
rs537785676 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994836 | AAAAAATAGCTGGGT[A/G]TGGTGGCGCATGCCT | 83860 |
rs537801336 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957358 | TAACTCTGGATGTGT[G/T]CTGCTATTGGTTTTA | 83860 |
rs537824495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000533 | GCACTTTGGGAGGCC[A/G]AGATGGGAGGATCAC | 83860 |
rs537837554 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992214 | TTTCTGAAATCACAA[A/T]ATCTTTTAGAAGTTC | 83860 |
rs537840504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900645 | GAAATGATTCAGATT[C/G]TTTTAATTACTATAG | 83860 |
rs537849847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7844067 | TTGTTTTAGAAAGGA[C/T]AGTAACAATTTGTTC | 83860 |
rs537851264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941244 | AATTTGCTGACAGGT[A/G]GAATGTCTTTCCTCT | 83860 |
rs537865267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004825 | TGGATTGGTATCTTT[C/T]GTCAGTTCTGTAAAA | 83860 |
rs537875560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852455 | TTTTCATATTTGTTG[C/G]AGAAACTGCGTTGTT | 83860 |
rs537889707 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:8007242 | CTATGTGTCAGCATG[C/G]ATAAATCAGGAGACA | 83860 |
rs537893653 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817828 | TCAAATCGCACACTA[C/T]AGCCCACAGGCAGCT | 83860 |
rs537937436 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934111 | CATGAATTCTGACAA[C/T]TCAAGGTTGAAAAAT | 83860 |
rs537997140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857033 | ATTTTCCCAACTTTC[A/G]TGTCCGTAAGCAAAC | 83860 |
rs538032627 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7968381 | CCTGCTTATAAAGCT[G/T]ATACCAAGAACCAAT | 83860 |
rs538046726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824904 | AAGAAAAATTGGGGT[A/G]GCTCTTTTCCTCCTC | 83860 |
rs538111701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906752 | TTCTACCAATAGGCA[C/T]CTTATGCCTTTATTT | 83860 |
rs538113694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913873 | AGGAAACACAGCAGA[C/T]AGAGATTAAGTGATA | 83860 |
rs538125911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942510 | ACAGTCTTGCTGATT[C/T]ACCCATAAAATTATA | 83860 |
rs538159258 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7975358 | TCATTGCTTCATATT[C/G]ATGCTTTACACTTAT | 83860 |
rs538201747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7962512 | AAGTCCTAGGATCTG[A/G]ATGCAATTTTACTAA | 83860 |
rs538203737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859153 | GTAGTCCCAGTTACT[C/T]GGGAGGCTGAGGCAG | 83860 |
rs538204421 | in-del | -/TCTCTGGGTTAGGCGCTGTTTAG | 0.317692 | 0.240661 | intron-variant | TAF3 | GRCh38.p7 | 10:7947335 | CAGCTGTGAGGGCCT[-/TCTCTGGGTTAGGCGCTGTTTAG]TCTCTGGGTTAGGCG | 83860 |
rs538234605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984377 | GGAGAGATTATAATC[A/G]AAGCATTTCCATCTT | 83860 |
rs538267074 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7989332 | GCAGGGGCAAGGCAA[A/G]TGGGTGCTGTGTAGA | 83860 |
rs538277851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871120 | ACTTGTTCTTAAACT[G/T]TATTAGTTCACTTAA | 83860 |
rs538289844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879455 | AATAATGACACCCAC[C/T]CTCATCTTTGTACAA | 83860 |
rs538293127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901398 | AAAGAAATTAATTAT[C/G]CAGTATGAAAACAAG | 83860 |
rs538327253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7920620 | AATCTGAATTTGTAC[A/G]ATATAAATCCCTTAT | 83860 |
rs538335319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941701 | AAAATAGTAAGTTCT[C/T]ATGGGGTCAGTAAAT | 83860 |
rs538345150 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7846045 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG | 83860 |
rs538357666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991579 | GCACAAAGGTCAGGA[A/G]TGTGATATAGATTTA | 83860 |
rs538365845 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867589 | GTCTGATGTCTGAAT[A/G]TGGAGGAGACAGGTA | 83860 |
rs538379359 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986001 | GTTGGCCAGGCTGGC[C/G]TCAAACTCCTGACCT | 83860 |
rs538390574 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7913988 | AAAAAGAGAGCAGGG[A/G]GGAACCATGATTGTT | 83860 |
rs538402517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7850620 | GGCAGAGGTTGCAGT[A/G]AGCTGAGATGGTGCC | 83860 |
rs538404528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858499 | TTTTTCACTAGTTCC[G/T]GATCTTACTGATTAG | 83860 |
rs538406061 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892278 | ATAAGCAGATTTAGC[A/G]TGTGCTGCCTGTTGG | 83860 |
rs538406274 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920255 | TTTATTTCTTGAGTA[A/G]ATAAATAATTTTTTA | 83860 |
rs538426119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7985850 | GTGCAGTGGTGTGAT[C/G]TTGGCTCACTGCAGC | 83860 |
rs538435738 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7920532 | GTTGATTTTTGTGTA[A/G]CCTATAATGAAATAG | 83860 |
rs538446073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7962445 | GTCTAAAATCCTTCT[A/G]GGTCCAAACTACCAG | 83860 |
rs538465860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7851525 | TTTTTTTTTATCATA[C/G]GAAATTTTCAAGCAT | 83860 |
rs538469067 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889783 | GTAAAAGCCTGGGTG[A/G]CCTCTTAATTGTTTC | 83860 |
rs538476973 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7864540 | TTGAAATGTGTTCCT[C/G]CTATCTAAGCGTAAT | 83860 |
rs538486926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7993573 | TCTGTTTACTTCTTC[A/G]TAGTGTCATTTAAAT | 83860 |
rs538502686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949631 | TGAAACAACTGTAAA[A/G]TTCCGTTGATCCTGA | 83860 |
rs538503022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7892861 | TCTCTCTTGTAGCCC[A/G]GGCTGGAGTGCAATG | 83860 |
rs538508501 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:8007032 | TGGTGAGGTGAGGAT[A/G]GCCATATTCCATGGC | 83860 |
rs538518820 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966151 | AAGCATGCAAAACCA[C/T]GGCACTATTTTAAGA | 83860 |
rs538538301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7844196 | TAATAAAGGCTTTGT[A/G]ATATCCTATCTGAAA | 83860 |
rs538548957 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7992769 | ACTTCTAAAAAAGTT[G/T]TTATTAATATTTTCA | 83860 |
rs538564871 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7886018 | ACTACAGCCTCAACC[A/T]CCTGGGCCCAAGTGA | 83860 |
rs538584943 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7970797 | TTTATTAAATTTAAA[C/T]GGTTTGTTCTTTAGA | 83860 |
rs538605318 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7838053 | CAGGTCCTAAAGGCA[A/G]ATGCTGCTATCATTC | 83860 |
rs538608680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886609 | AGGGTAATAATATCT[C/T]ATGGGGTTAGTGTAA | 83860 |
rs538621591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7993879 | AGGATAAATATACAA[C/T]CTTTTTTTTTTTTTT | 83860 |
rs538635121 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995467 | TTTTTATTATTATCT[G/T]TCTAGTGTATCTCAT | 83860 |
rs538635266 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7838730 | TGAATACCTTCTGGC[C/T]CCCTAACATCCGACG | 83860 |
rs538637413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919907 | TTGTTAGTCCCCCTC[A/G]TATTCTGTAATGAGT | 83860 |
rs538649245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7832080 | TAATGATTTTCAAAT[A/G]TGTAATACATTATTA | 83860 |
rs538655175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7935253 | CTGCACTCCAGCCTG[A/G]GCAACAGCAAAACTC | 83860 |
rs538676057 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902893 | GTACCCTTTTTTAGT[A/G]GTTAGAATAGACTCA | 83860 |
rs538697159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839117 | TGCCCCTCGTTGCTT[C/T]GTGCTTTACCTTCCA | 83860 |
rs538701357 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7887275 | GGTTAAGGAAATGAT[C/G]AGGAAAACTGAATCT | 83860 |
rs538707285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832787 | ACCCCTGGCCTCAAG[G/T]GATCTGCCCACCTCA | 83860 |
rs538711841 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821495 | GAATGTCAGGAAACA[A/G]CAAACTGATGGTGTT | 83860 |
rs538782560 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991600 | TATAGATTTATACAC[A/G]TACACACATGCATAC | 83860 |
rs538802121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929956 | CCTATAATTCCAGCA[C/G]TTTGGGAGGCCAAGG | 83860 |
rs538821318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899923 | TATGGGGTTATGGTG[A/G]TTTTTAAAGGCAAGT | 83860 |
rs538832928 | in-del | -/GC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858825 | TGTGTGTGTGTGTGT[-/GC]GTGCGCGCGCCTGCA | 83860 |
rs538853264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818950 | TCTCCCTGTCCCTCC[G/T]CGTCCCCGGGGTGTG | 83860 |
rs538894928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859319 | AAATAAATAAATAAA[A/T]GAGAAGTGTGATGCC | 83860 |
rs538948424 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7968481 | GACCTGGAATAAGAT[A/C]CAGGACAAGTTTTTT | 83860 |
rs538970656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901480 | ATGTTGTTTTTGACC[A/C]ACCAACCATTGAAAA | 83860 |
rs538971782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832749 | GAGATGCGATTTCAC[C/T]ATGTTGGCCAGGCTG | 83860 |
rs538992743 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7853184 | AATCATATAAACTTA[C/T]AATTAAATAAATTAT | 83860 |
rs539039567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949724 | ACCAAAACATTGCCA[A/G]TTAGACTGTGAAGCA | 83860 |
rs539062554 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986150 | TTTTTTTCCCCCTTC[G/T]TTTCTTTTTGCCCTT | 83860 |
rs539069205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895420 | TCCTTAGACATCCCA[C/T]GGCTCTGTTTTTAAG | 83860 |
rs539101370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949205 | AAAGAGGAAGGGGCT[G/T]GTTCTGTAAATCAGA | 83860 |
rs539124717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951764 | TCTTACTGTTACTCA[A/G]AAGCCAAAGAGGTAG | 83860 |
rs539143934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880521 | CCACAGTTAAGTAAC[A/G]GAAACCTGTATTGGA | 83860 |
rs539149662 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962640 | CATCTGACCCTTTGT[C/G]CTGGACTTCACCACT | 83860 |
rs539171897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839932 | AGCATACACAGATTG[A/C]GAGGGACTTTACAAA | 83860 |
rs539187447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7966217 | TTTTCTTTTTGGTGC[A/G]CCATTTTGGCATGTG | 83860 |
rs539192025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835903 | TTGGGAAGATGCACA[A/G]ACTACCTTGCCCCAG | 83860 |
rs539195998 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935370 | TGGGAGGCCGAGGCG[A/G]GCAGATCACGAGGTC | 83860 |
rs539198351 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866244 | CTTCCAGGCACGGGG[C/G]ATGGAGCAGTCAATA | 83860 |
rs539199961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934038 | GATGCTCATTGAGCA[C/G]AAAATGCCACCTTTC | 83860 |
rs539203496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842547 | AAGATTAAACAATAA[C/T]CTTAAATTTTTTAGA | 83860 |
rs539221582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978574 | CTGTGGATTCAGTGC[A/T]TTTGAAACCAGCTAT | 83860 |
rs539221744 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7930139 | GGAAGTCAAGACTGC[-/A]AGTGAACCGTGATTG | 83860 |
rs539231841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826109 | GTGTGTCAGGGTTGC[C/T]TCATCTGAAAAACTG | 83860 |
rs539238193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937180 | GGACATAAGTTTTCA[G/T]TTCATTTGGGTAAAT | 83860 |
rs539247103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910329 | GCTACAACATACAAA[A/C]ATCTAAATATCAGGA | 83860 |
rs539252838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865459 | ACTCCAGCCTGGGGG[A/T]CAGAGTGAGACTCCG | 83860 |
rs539269957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7940185 | GAAATAATTTCAACC[A/T]TAAATTCTATTTTCA | 83860 |
rs539275099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986478 | ATGGAGGCAAAAACT[A/G]TCTAATAGAATTGGG | 83860 |
rs539285114 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912559 | AAGTAAGACTGAAAA[A/G]CAAGACCTAACCCTT | 83860 |
rs539289569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868456 | GCAGCCAAGCTCTAG[C/T]GACCATCAGGAGTGG | 83860 |
rs539294662 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940965 | CCTGTCTCAAAAAAG[-/A]AAAAAAAAAAAGAAG | 83860 |
rs539300258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943703 | CTTTTTCACTTCTGT[A/G]CCAACCAAATATAAT | 83860 |
rs539309946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822510 | AAAATCAAAGACTGC[A/G]GAAGTATGTGGAGTT | 83860 |
rs539318790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994702 | AGGCACAGTGGCCCA[C/T]GCCTGTGATCCCAGC | 83860 |
rs539324989 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7968397 | ATACCAAGAACCAAT[-/A]AAGATGTGATTAATT | 83860 |
rs539330169 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7894162 | GCAGGGGTTTGTAAT[C/G]CAAAGTTAGAGTCCC | 83860 |
rs539330312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946918 | AAACTTTTCTTTTTT[A/T]AAAAAAATAATTATT | 83860 |
rs539336388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852593 | GCTTGATGAAATGTC[A/G]TGTTCAATTGTTTTG | 83860 |
rs539349851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862739 | TGTCATTGTAGATTA[C/T]TTTGCATTTTTCTAG | 83860 |
rs539353007 | in-del | -/TG | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:8011103 | AGCCATTGCCATTGC[-/TG]TGACTACCAACTCTG | 83860 |
rs539362188 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887527 | CTGCTGCTTTTAGGG[A/C]AAGGAAGCCGGAGAT | 83860 |
rs539376686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7904357 | AGCCCTAATACAACT[A/G]AAATGAAATGATCTT | 83860 |
rs539401344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856373 | TAATCCCAGCTACTC[A/G]GGAGGCCGAGGCAGG | 83860 |
rs539449947 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005966 | ATTTATGCAAGATAC[A/G]TAATCTCTCTGTGCC | 83860 |
rs539455282 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:8004313 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACGGGCA | 83860 |
rs539473949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890447 | TCCTATTAGAGTTGG[G/T]TAATCGCAGAAAAGA | 83860 |
rs539482545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7863987 | AGAAAGTACAGAGTT[C/T]CTAAATTCATCCTGC | 83860 |
rs539501080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7975128 | GTGGAACAGAAAGAC[C/T]GAAGATACTGTAAAT | 83860 |
rs539501865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842104 | GTGAGTACCCTATTT[A/C]ATTAAAGATGGCCCT | 83860 |
rs539507913 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911011 | TTTGATATTTTATTT[G/T]CCACATTCTTAGCAC | 83860 |
rs539508565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7960082 | TCTAAAGACCCGTTA[C/T]CCTGCCTAAGCCAAA | 83860 |
rs539517098 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817296 | TGTCCAGGGAGTAAA[C/T]GCAGGCACCTTGCCC | 83860 |
rs539535318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7926581 | TTCTTCCATGAGTTA[C/T]TGTCTGTTATGGAGG | 83860 |
rs539566049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958933 | AGGTCAGGACATCGA[G/T]ACCATCCTGGCTAAC | 83860 |
rs539592241 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7867808 | CCTGTGCAGAAATTC[A/T]TGTGTAACTTTTGAC | 83860 |
rs539595707 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960192 | GTAATATTAATAAGT[A/G]AATGTTCATTCACTT | 83860 |
rs539605287 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932803 | CCACCTCAGCCCCTA[G/T]AGTAGCTGGTAATAC | 83860 |
rs539610043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000056 | GTGTATAACTCAAGC[C/T]ATCCTTAAAAATTCC | 83860 |
rs539630046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981908 | TAATCTTTAAAATCA[A/T]TATGTATAGACACTT | 83860 |
rs539641916 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009357 | CCGCCCGCGCGGTTA[A/G]CATGGAGACGTTTTC | 83860 |
rs539652565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7836375 | CGGCTCCCTGGTTCA[A/G]GTGATTCTCCTGTCT | 83860 |
rs539656551 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7925665 | AAAAAATTAGGCATG[A/T]TGGTGTGCCTGTATT | 83860 |
rs539678736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862120 | GTAGAGTTACCATCT[A/G]GTTTGTTTTTAGAGT | 83860 |
rs539678948 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841179 | TTTCAGATAAAATAA[A/T]AGCAAGTTATTTGCT | 83860 |
rs539693291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981290 | ACCCACCCTTGCCCT[C/T]GGGCAGTGGGTCCCC | 83860 |
rs539694976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7989770 | TTGGTATAAAACCCT[C/T]TGACCCCAGATGCAG | 83860 |
rs539696081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7939428 | ACAATGTAGCCCGCC[A/G]GTTAGCAAAGTCCCA | 83860 |
rs539707930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954183 | TCAGAGTGCACTCCA[C/T]ATATGAATGAGTGGA | 83860 |
rs539740073 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7855937 | AAAAGGAAAAAAAAA[A/G]AGACAAAAAAAAAAT | 83860 |
rs539753870 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861599 | TGATTTTTTTTTTCA[A/T]TTTAGCACTTTACAG | 83860 |
rs539759437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7946300 | ACACAAAACTCGTTA[C/T]GCAGTATGGCTGTCC | 83860 |
rs539775017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831070 | ATTAATTCATTAGGG[A/G]TTACAAAGTAATGAT | 83860 |
rs539781847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919068 | TGGACATAGAGGAGA[G/T]TTTGCTAATGACAGA | 83860 |
rs539798849 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8012617 | GTACGGGTGACTGCT[C/G]GTTCTCACCCCTTGT | 83860 |
rs539832079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883712 | GAAGATTTTCCCCTC[A/C]TTCCCACTTATTTAT | 83860 |
rs539837583 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987331 | CAAAAAAAAATAAAA[A/G]AAGAACTTAGAATTA | 83860 |
rs539850042 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983782 | AACTCAAGGCTACAG[C/T]GAGCTGTCATTGCAC | 83860 |
rs539850822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835970 | TTTTTGCTGCTTTCA[G/T]CACTGTTGGGCAATT | 83860 |
rs539901572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7905758 | CGTGGTGGCAGGCAC[C/T]TGTAATCCCAGCTAC | 83860 |
rs539914987 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010302 | CAGCCTCCATAAATC[A/G]TATCAAAGCTTGTTT | 83860 |
rs539920468 | snp | C/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7918048 | TTTGTTTTTAGGATT[C/G]GGATATTATGGCATA | 83860 |
rs539946437 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843248 | TAGTAGCTGGGACTA[C/G]CAGCTTGCACCACCA | 83860 |
rs539986713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991002 | CTCTCAGATGCCTTC[A/T]ACCCTTTTAAGACCT | 83860 |
rs540051843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999434 | AGGCTGTTAAAAAAA[A/G]AAAAGAAAGAAAGAA | 83860 |
rs540057600 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956834 | GACTGTGTGAAAAAC[A/G]TGAAAAAATAGGGTT | 83860 |
rs540097455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897994 | ATTCTTATTGGTTGG[A/C]TGTTGAATCTCTTGA | 83860 |
rs540098917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918536 | AGAGCTGGGAGCATG[A/T]CGGGAATGTGGGTCC | 83860 |
rs540126184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005823 | CTCCTACATTACATG[A/C]CTTTTATGTAAGGCA | 83860 |
rs540159292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823491 | AAAAAAAAAAATTAC[C/T]CAGGCATGGTGGCAT | 83860 |
rs540203110 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7933408 | TATCCAGTGTGGAGC[A/C]AAAGGCTGCACGACG | 83860 |
rs540204664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973140 | CCACACCTACCCTAT[A/G]GAGTTGTGAAGATAG | 83860 |
rs540206295 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839517 | CCAAAGTCACATGGC[C/T]GCGAAGTGATAGAGG | 83860 |
rs540220055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876032 | TAAACTTTTAAATTT[A/G]TATTTATAAAAAGGA | 83860 |
rs540227590 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7844796 | TTATTTATGTTCTGC[-/T]TTTTTTTAACGTATC | 83860 |
rs540231990 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7932498 | GGGAGGAGAGAGATT[C/G]ATTATGAGTCTGGGG | 83860 |
rs540232586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947350 | TTCTCTGGGTTAGGC[A/G]CTGTTTAGACTCTGG | 83860 |
rs540261028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980856 | GGCAAAGCAGGCACC[A/G]GGTTATTTGTCCTCC | 83860 |
rs540291745 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7938804 | TTGAAAGAGACTGCA[A/G]GTTGATCAATAACTG | 83860 |
rs540316184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988428 | AACCCTGTTTCTACT[A/G]AAAATACAGAAATTA | 83860 |
rs540326417 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859615 | CTCCATTTGCCCTCC[A/G]TTTGAGAATGAAGTG | 83860 |
rs540346286 | in-del | -/GCAATTGTATTACTAGGACTG | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7884754 | CATTGCTATTACAAT[-/GCAATTGTATTACTAGGACTG]GTCATTGCTTTTAGT | 83860 |
rs540348185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953124 | TTCCTGGTAGTAATA[C/G]CCCGTGTTCTACACT | 83860 |
rs540348785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830730 | CTCAAGTGATCCGCC[A/C]GCCTCGGCCTCCCAA | 83860 |
rs540361723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945977 | TTAACAAATATTTGT[G/T]GAATGAATGGATGGA | 83860 |
rs540385875 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7847357 | TGACAAGAACCTAGA[C/G]CATCCTGTTCTGAAA | 83860 |
rs540391189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960954 | CAATTTCCAAGGGAT[C/G]CCTTTTACAAACTGC | 83860 |
rs540396699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975493 | GTATTGGAGGCATAC[A/G]TGAAGCTGGAATTAA | 83860 |
rs540404651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7968149 | CTAAAGTGAGACATA[C/T]CTGCTCACTTTATGT | 83860 |
rs540415116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7823576 | AGAAGTTTGAGGCAG[C/T]AAGGAGCTGTGATCA | 83860 |
rs540450037 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7847898 | GCTGAGCCTCCCGAG[A/T]AGCTGAGACTACAGG | 83860 |
rs540478212 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7934859 | CAAAAATATTCATTG[A/G]GCCCCTCCCATGCGG | 83860 |
rs540495379 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7941419 | ATTATTTGTAACTGC[A/T]CATGAGGATGCTACA | 83860 |
rs540509270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841730 | GAGGATGTGCTACAG[A/C]GAGGAGCCTAGGTTT | 83860 |
rs540513064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7849094 | CGCAACAACACTTAC[A/G]TGTTTCCTTAGGTAC | 83860 |
rs540541908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973928 | AGATCAGGAGTTTGA[A/G]ACCACCCTAGCCAGC | 83860 |
rs540563786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991090 | CTTTCATGTGAATCT[A/G]AAGTCAGTGTAATAA | 83860 |
rs540568775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7906434 | AAACCTGCTGCTGCA[C/T]TGGGGAGGGGAACAA | 83860 |
rs540568785 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933362 | CCCAGAGCAGTAGCT[G/T]CATGCATGGCACCCA | 83860 |
rs540575956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857937 | TTTTTCTGCTAACCT[G/T]AGGGATTTCTCAGAA | 83860 |
rs540578984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853578 | TTCAGCAAAGAAGTT[A/G]CTCACATCATTGACA | 83860 |
rs540590477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990464 | TGCCTTCAAAGTACG[C/T]GGTCAGGGTAAATTT | 83860 |
rs540598745 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849554 | AAATGTGCATAATAG[C/T]TGTGGCTTGGAAAAT | 83860 |
rs540621573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954310 | TAGTGAGATTCAGAG[A/T]GCACTCCATAGGCGA | 83860 |
rs540642117 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955993 | GTTCTGCAGTCACAC[A/T]CTGATGCTTTTAGGG | 83860 |
rs540663545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7998794 | CAGTGAGCCGGGATC[A/G]CGCCACTGCACTCCA | 83860 |
rs540686367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7956493 | CTCCATCTCAAAAAA[C/T]AATAATAATTTTAAA | 83860 |
rs540713750 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995548 | CCCTTTTAGAGATTT[C/T]ATGATTCGGAACATT | 83860 |
rs540731578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887715 | GAAAAGGCTTCAATC[C/G]AAGCTAAAATCGGGG | 83860 |
rs540750431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956080 | TTAGGTAATTATATT[A/C]ATAGATGTAGTTATA | 83860 |
rs540788227 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883690 | TCAGTTGGCATTCTA[C/T]TCTATGGAAGATTTT | 83860 |
rs540795649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869606 | ACACACATCCATTTG[C/T]GTTTTCTCATAATTT | 83860 |
rs540824907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904795 | TTTTTTCCAGATTCT[C/G]TGGAAAAACTGGAAG | 83860 |
rs540836409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826381 | AATACTAGCAAGGAA[A/G]TGTAACTAAGATAAC | 83860 |
rs540839650 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903434 | GAAGCAACTCTTTCT[A/C]CAGGAAGCTCACCTC | 83860 |
rs540878452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907861 | ACAGAGGGTGGGTTG[A/G]AGCTGGAAAAGCCAA | 83860 |
rs540880530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819161 | TCTGAATTGTGTCTG[G/T]ATCTCTCTCATTGTC | 83860 |
rs540896967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7859854 | TGTTGGACAAATGGC[C/T]GTTTCCCAGATAACT | 83860 |
rs540937822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7936866 | GTACCCGCTGGCATC[C/T]ATTGATTTTTTTTTT | 83860 |
rs540955470 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7899029 | TTTTTCTTTTATTCT[A/C]GGTGAGATTCCCCCA | 83860 |
rs540955601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905971 | TTTGGTAGAAAGTTA[C/T]ATTCAAAAGTTTGTT | 83860 |
rs540957831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7940746 | GATCATTTGAGCCCA[G/T]GAGTTTGAGACCAGC | 83860 |
rs540960153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986178 | CTTGGTACAGTAACT[C/G]TGTTTCTTCTTCGTA | 83860 |
rs540960879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950643 | TATATACAGTTATCC[G/T]CATTATGCACAGATT | 83860 |
rs540964504 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895740 | CTCTATCTACAGTTA[C/T]AGAATTTTTGCTTTC | 83860 |
rs540981913 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8002256 | TCACTTGCTCTGTTT[C/T]TTCTCTTTTCTTTTT | 83860 |
rs540984012 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903877 | TCTCTCGGGGGACAT[A/G]AGGGACATAAGACAA | 83860 |
rs541001208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943538 | TTCTGTTCTAGCTGC[C/T]AGGAGTGCCTGAGAG | 83860 |
rs541055178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7867886 | AATAATGTAAACGGT[C/T]GATTAACACGTATTT | 83860 |
rs541067366 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833850 | CCCTTCCTGGGGACC[A/G]AGGGCTTCCTGGGGA | 83860 |
rs541090095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895703 | TTCCATTGCACACAT[A/T]TTTTTCCACTAATTG | 83860 |
rs541097995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903364 | CATTTTCTTACTCTT[C/G]TGGCACAAGAAGCCC | 83860 |
rs541106751 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:8008327 | TGGTCTTGAACTCTC[A/G]ACCTCAGGTAATCCA | 83860 |
rs541111680 | snp | A/C | 1.66322e-05 | 0.00288371 | missense | TAF3 | GRCh38.p7 | 10:7964330 | ACACCTAAAACAAAG[A/C]CTAAAACTAGCTCTC | 83860 |
rs541114690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8010862 | GCAGTGAGCCAAGAT[C/T]GTACCACTGCTCTCT | 83860 |
rs541138056 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7910522 | AGTAGCTGGGACTAC[A/T]GGTGCCCGCCATCAC | 83860 |
rs541143950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888168 | AAGTTTTTCCTGAAC[G/T]CTGTCTTCCTCTAGG | 83860 |
rs541152369 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016882 | ATGATTTTATAAATG[G/T]TCTTTGCAATAATAA | 83860 |
rs541169709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8007838 | ATAGGTCCTCAATAA[A/G]TAGTGCTTTTTATAA | 83860 |
rs541224867 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8006128 | TGAAGTCGGGAGTTT[C/G]AGACCAGCCTGCCCA | 83860 |
rs541228605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937503 | TTTGGTAAAGTGTCT[G/T]TTCAGGTCTTTTGCC | 83860 |
rs541230497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914790 | TCTTTAGTGGTTGGC[A/C]CTTGTCATTAGTCTT | 83860 |
rs541250596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865639 | CCCGGCAGGGTGGAT[A/G]CAGCCACGTGCAAAG | 83860 |
rs541251337 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983190 | CAGTCCCTGGCGAAG[C/T]CCCGCTTCCCGGGCC | 83860 |
rs541254546 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899503 | TCTTTCCCTCTACAG[G/T]TAAACCCAGCCATTC | 83860 |
rs541284722 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948154 | TGCGACCTCGAACTC[G/T]TAGGTTCAAGCAATC | 83860 |
rs541287064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7840895 | GCTCTTGTTGCCCAG[A/G]CTGGCGTGCAATGGC | 83860 |
rs541289708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944200 | GATTGTCAATTTTAT[C/T]TTCTGTCTACTTACT | 83860 |
rs541302157 | in-del | -/AAAC | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7912425 | GTTTTTATGGGTAAG[-/AAAC]AACATGGAATAGTGG | 83860 |
rs541312367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860502 | ATGAGTGTATTTGTA[C/T]ATTTTATGGAATTAT | 83860 |
rs541314384 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933520 | GATAACATCTTCAAG[A/G]GAGTTTCTGTGCTGG | 83860 |
rs541325648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7959007 | TAGCCGGGCGTGGTG[A/G]CGGGCGCCTGTAGTC | 83860 |
rs541335232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7875194 | GTCATAATTGTTCCT[C/T]CTCGATATTTTTTTT | 83860 |
rs541347234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834782 | AATATTGCAACTGAT[A/G]CTATCATTCATGATT | 83860 |
rs541362297 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877554 | TAAGAATGTAATGAG[A/C]ATATGGCATTTATTG | 83860 |
rs541365605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8009910 | CAGGCATGAGCCACC[C/G]TGCCCGGCTTTTTTT | 83860 |
rs541369263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901975 | GATTTGTGTGTGCAC[A/G]TGGACGCTCCTCCAG | 83860 |
rs541423453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909749 | TTACCACTTTATATC[C/T]TTATAAAGGTATCTT | 83860 |
rs541441111 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7840429 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCGCG | 83860 |
rs541458664 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7951339 | CATGCGGCTCTTCTG[C/T]TGGACGAGGCTGGGA | 83860 |
rs541463960 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7832855 | GCACCTGGCCCAGCA[-/T]TTATCATTTCTTTGT | 83860 |
rs541475128 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7847075 | ATTGACATGTTTCAC[A/T]GTTATTAAACAAATC | 83860 |
rs541495440 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910096 | TTATTGGTTTTTTCC[C/G]CTCAAATATTTTGTA | 83860 |
rs541504458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840942 | GCAACCTCCACCTCC[C/G]AGGTTCAAGCTATTC | 83860 |
rs541512093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7822221 | AGAATAGAGAGAAAG[A/G]AAAAAAATCTGAAAT | 83860 |
rs541574884 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7896827 | CATCTAGATTCTCTC[-/T]TTAAGGTCTAACAAG | 83860 |
rs541614853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820323 | CCAGGAGAAAAATTG[A/G]TTATATTTGTATTCT | 83860 |
rs541615512 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7834343 | TTTCAAGTCTTACAT[A/T]TAGGTCTTTATTCCA | 83860 |
rs541638607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945429 | TGACTTACCTAATTT[A/G]TCTTGTTTACCTGCA | 83860 |
rs541662909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923619 | ACAAAAAAACCCCTC[C/G]CCCAACAGTTGCTTT | 83860 |
rs541695736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938075 | GTGAAGTATGAATGT[C/T]TTTATTAATAAAACA | 83860 |
rs541709063 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7827577 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 83860 |
rs541727327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924221 | AGAAATGGAAAGCCA[A/G]AACTTCTTTTTTGGT | 83860 |
rs541735005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958203 | TTCCAAACACTTAAA[A/G]CATAGAATTAAAATT | 83860 |
rs541758047 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826326 | GCATGCAAATATTCC[A/G]TAATAAAATTCTCTT | 83860 |
rs541764537 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7833474 | ATTTTTTCATGTATT[A/T]GTTGGCAGTTTGTAT | 83860 |
rs541789045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903147 | ATCGCTTGAGCCTAG[A/G]AAGTCGAGGCTGCAG | 83860 |
rs541805151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898316 | CTTTGGGAGGCCAAG[A/G]TGGGTGGATCACCTG | 83860 |
rs541810988 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880017 | AAGTTTGAGACCAGC[C/T]TGGGCATATGGCAGA | 83860 |
rs541835593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888198 | GCCAGGATCTACACC[C/T]CTTCCTTGTTTTACA | 83860 |
rs541835643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896289 | GAATGGGGGGAAAAC[A/G]TAGACCAAAACCAAT | 83860 |
rs541837148 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867752 | TAGATTTTTATTACA[A/G]AGTTGACCCTTGAAC | 83860 |
rs541878844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002743 | ATCTTTGCTGGTTTT[C/T]TGACTGCTTATTCTG | 83860 |
rs541880607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995358 | TCCAAAGTGGAAGCT[A/G]TATAACAAAATACAT | 83860 |
rs541893858 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999790 | TACGAAAATACCATC[A/G]TTGTAGGAGGTTTTC | 83860 |
rs541924993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882278 | TTTGGTCAATCTAAC[A/G]TGTATTCCTCATTTA | 83860 |
rs541939726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856472 | GCAGATGACACAGGA[C/T]TTCATCTCAAAATAA | 83860 |
rs541939996 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880704 | CCTCATCTAGGTGGA[G/T]TTTTTTTTAGTAGTT | 83860 |
rs541941811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002303 | ATCCCGTATTTCTCT[A/C]ACCTGTGCTTTATCC | 83860 |
rs542007622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866266 | CAGTCAATAAATAGG[C/T]AGGCTCTGCTTCCAT | 83860 |
rs542013089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909063 | TGTCCCTTACCAGCC[A/G]TCGCTGGGCCTGTCA | 83860 |
rs542019131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7931475 | TGTGACATTGCATCT[C/T]GGGGAATTTCAGCCC | 83860 |
rs542032644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883068 | AATAAGGAAATTAAC[A/G]TTGATACAATACTGT | 83860 |
rs542044453 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983144 | CAGAGGTGGTCCTGG[C/T]CACTCAGGCTGTTGT | 83860 |
rs542053757 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7979733 | TTAAATTAAAATAGA[G/T]CGAGAAAGAAAGAGG | 83860 |
rs542080419 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006903 | GGTTCTCACTACAAC[C/T]CTCTGAGGCCACTGC | 83860 |
rs542087095 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842896 | CTCAGCACTGAATGT[A/G]ATGGTTGTCATACTT | 83860 |
rs542094876 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835548 | GCTGTGTCCTCTCAG[C/T]GAGGCTCTGTCCTGG | 83860 |
rs542096894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854400 | CACTGTTATGCGAGC[C/T]GCAGCGAGATACACA | 83860 |
rs542112614 | snp | C/T | 5.05157e-05 | 0.00502546 | missense | TAF3 | GRCh38.p7 | 10:7965056 | GAGAAAACCAAGCTG[C/T]CTTCCTCCGTGGAGG | 83860 |
rs542115489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987410 | TGAACATTTTTCCAT[A/G]TCTGTATGACATGGT | 83860 |
rs542116838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996684 | TTACGTTGAGGCAGG[G/T]TCTCACTCTGGGATT | 83860 |
rs542124349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952867 | AGTTGTGTTTTAAGG[A/G]TCTAATTTCTGTTAC | 83860 |
rs542149002 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7942803 | ATTTAGTTAAAAAAA[A/T]TTTTTTTTGTCGTTT | 83860 |
rs542170855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7895733 | GTGTGGCCTCTATCT[A/G]CAGTTATAGAATTTT | 83860 |
rs542212787 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918632 | GGGGGCAGGCCTCCA[G/T]ACATCAGTCAGGAAG | 83860 |
rs542228556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010630 | TTGTAAAACCAGCTG[A/G]ACGCAGTGGCTTACG | 83860 |
rs542230947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997664 | AATCCTCCAAAAGCT[A/G]TAATGCTGGCAGCAT | 83860 |
rs542234761 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829153 | GCCACTTTTAGAGTT[A/T]CTATTTTTTAAAATT | 83860 |
rs542242556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865164 | AGTGGAGAGGGCAGG[A/G]AATAGTGGTTCAGAA | 83860 |
rs542243379 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7962102 | GTAATCCTACTCCCT[C/T]GGCCTCCCAAGATGT | 83860 |
rs542266624 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950385 | GAAGTTCGGAGAATA[A/G]TTGTGTGTCTCGAGC | 83860 |
rs542277586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897261 | CTTAAGCCAGGTCGC[C/T]GGGGGGTCACTTTTA | 83860 |
rs542280310 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945453 | ACCTGCATAGTGAGC[A/G]TTTTAAGACCTTTCC | 83860 |
rs542282305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013899 | AGCCGCTCCTGAGAT[C/G]AAGCATCCACTGAGT | 83860 |
rs542283191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900315 | ATTATTGATAAATTA[C/T]ACTTTTAATGGAGGC | 83860 |
rs542328485 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824021 | GTGTCAGGTGCTGTT[C/G]CAGATGCTTTTGATC | 83860 |
rs542347940 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7852091 | GCCAAGCCTTTCCCC[C/G]ACCATCTCCCAGAGA | 83860 |
rs542361415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924312 | ACCATGAAAGAAAGC[A/G]GTGGTTCTCTGCTAG | 83860 |
rs542383398 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7993019 | TAAAATATACAGACA[A/T]TTTCCTTGTTACCAT | 83860 |
rs542395181 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901460 | TTTTTAGTGCTTGCT[A/C]TTTAATGTTGTTTTT | 83860 |
rs542444438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946475 | ATGCCTGTAATCCCA[A/G]CACATTGGGAGGCCG | 83860 |
rs542447046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992211 | GCCTTTCTGAAATCA[C/G]AAAATCTTTTAGAAG | 83860 |
rs542454766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916350 | ATGTAATTAGCCTTA[G/T]GCACCATCACCCTGC | 83860 |
rs542460015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7831595 | GTGATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGC | 83860 |
rs542463224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870526 | TTTTAATGTAAACTT[A/C]ATTTTTCTATTGATT | 83860 |
rs542476246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821397 | ACTGAGCATCACTTA[C/T]GAACCAACCCCTGTA | 83860 |
rs542505593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946073 | TGGGGCTGAAGCCAC[A/C]CTCTCGGGTCATCCA | 83860 |
rs542508098 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8000242 | TAGCCTCAGCCTCCT[C/G]AGTAGCTAGGATTAC | 83860 |
rs542519751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917050 | TCAGCGAATATTCAT[G/T]GAGAACATCTCTGTG | 83860 |
rs542539296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952048 | ATAAACTGTATCCTA[C/T]GCATAGTCTTACTAT | 83860 |
rs542578569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7954908 | ACAGAGCTCTCCATA[A/G]TGAGATTCAGAGTGC | 83860 |
rs542595447 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002707 | CATAGAGTCAATTTC[A/T]TTATTCTTATTCAAA | 83860 |
rs542627407 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7922438 | TTCTGTAAAACATAG[A/G]TGATTATCAAGTGAT | 83860 |
rs542651159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914058 | TCCTCTTTTAGATAC[C/T]GATTCAAAGAAACTG | 83860 |
rs542672988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907586 | ATTATGAGGGTAATA[C/T]AATAGCCAGAAGTTT | 83860 |
rs542690411 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7914919 | TGCCCCTGAAAGCCT[C/T]GGTGCTCCCAGCCTT | 83860 |
rs542690637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7923379 | GTTATAGGTTTTGTG[C/T]GTGTTATGAAAATGG | 83860 |
rs542691069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928022 | AATTATTTGTTTTAC[A/G]GCCTCTAACATTTTA | 83860 |
rs542754078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915372 | ATCATGGGCCGGGCG[C/T]AGTGGCTCACGCCTG | 83860 |
rs542754455 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7935335 | AGGCGCGGTGGCTTA[C/T]GCCTGTAATCTCAGC | 83860 |
rs542773437 | in-del | -/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817017 | CACGTGAGTCTATGA[-/T]TTTGTTTCAACTTTT | 83860 |
rs542779958 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968934 | CTTTTAGTTCCCCTT[C/T]GTGGGCAGTCAGACA | 83860 |
rs542781690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827362 | ATAAAATTGGACAGT[A/G]TTTAACATATAAAAT | 83860 |
rs542790330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927230 | AAATTTGCAAAGGGG[A/T]GGATAATGAGCACAA | 83860 |
rs542793680 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7908420 | AACTTTAAGCATTGG[C/G]AACTTTAAATTCTAA | 83860 |
rs542802815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894005 | TACAAAACTCAAGTT[A/C]CTCCAGCTGTAGTCT | 83860 |
rs542818821 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997158 | AATGTTGAACTTCCT[G/T]TTCAAAAGTTTCTAT | 83860 |
rs542838252 | in-del | -/T/TT | 0.497271 | 0.0368399 | intron-variant | TAF3 | GRCh38.p7 | 10:7823634 | GCAAGATGCCATCTC[-/T/TT]TTTTTTTTTTTTTTT | 83860 |
rs542844765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956663 | GAATCTCTAGCTGTG[G/T]TGATGAATTTGTGCT | 83860 |
rs542853223 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011596 | TTAAATTTCCTTAAA[C/G]GAGTTTTGGAAGGAA | 83860 |
rs542853295 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7854529 | ATATGGATTCAGAAT[-/G]GGGAAAGACTTCTGT | 83860 |
rs542856777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879007 | TGCTGGGATTACAGG[C/T]ATAAGTCACCGCGCC | 83860 |
rs542859704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919207 | CTAGCTTCTGGCTAA[A/G]GTAATGGGGGATGTA | 83860 |
rs542866303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886918 | TTTATTTGAAATGTT[A/G]TCTTTTATATTTAAG | 83860 |
rs542870872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7832373 | CAAATGACAAAATTT[C/T]CTTCTTTTTTTAAAG | 83860 |
rs542877597 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8008488 | AATGGCATTGAGAGT[A/G]TTAAGAAGAAACATT | 83860 |
rs542902958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948897 | AATGGTTTTGTTAAA[A/G]TCTCCAGGATTATAC | 83860 |
rs542926449 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7962595 | TTCTGTTTCTCTTAC[A/G]CTCCCCGTGTTTCAC | 83860 |
rs542943156 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844559 | TTTTTTTGTATTTTA[A/G]TAGAGATGGGGTTTC | 83860 |
rs542948797 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920666 | ACTGCCATTTTAAAA[A/G]TCAGAATTGAGATGA | 83860 |
rs542970415 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7825116 | CAATTGCAGAGTTCC[C/G]TTTTTTCCTGCATAA | 83860 |
rs542975092 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7864645 | ATGGTGGGGTTATAC[A/G]GCTTGTTTGTCTTTT | 83860 |
rs542983556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880593 | TAATCCTGCTGACGT[C/T]GTTTCCTTTAAGGGC | 83860 |
rs542984469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913567 | GAACTCACCACCCAA[G/T]CTGGCAAACCTATCT | 83860 |
rs542984982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859783 | TGTCAATTTTATTCA[C/T]TGTTTCATTCCTAGC | 83860 |
rs542989454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7977924 | ATCAACCCACTCGTC[C/T]TTACAGTTAATCTGT | 83860 |
rs543012262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833726 | AAAGGCTCTGAAATT[A/C]TTCTCCTCAGTGGTG | 83860 |
rs543044980 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893511 | CTTACTGTACCAAAC[A/T]TTCATATCCTCAGGT | 83860 |
rs543064864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962796 | TTCTGTGGGCTAGAC[A/G]TATCTGTTATTGCTG | 83860 |
rs543073612 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7826456 | TTTTTTTTGTTTTGT[G/T]TTGTGTTGTTTTGAT | 83860 |
rs543075749 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921261 | TTTGGTAGTTTTTCT[A/G]TCCTTTCCACTTTAG | 83860 |
rs543111898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853512 | TGTTCCATTGTAAGT[A/T]GTACCAAAAATGGTA | 83860 |
rs543152450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845498 | ACTGAAATGATTTGG[C/T]TTGGGTGGTTCTGTT | 83860 |
rs543155682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865678 | AGGTTCATTCTTAGA[A/G]TTAGGCTTTCACAGG | 83860 |
rs543181522 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014088 | TCTTATTAAAAATAA[C/T]AATACTAAAAGGAGA | 83860 |
rs543187537 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7986141 | TGGACTTATTTTTTT[G/T]CCCCCTTCTTTTCTT | 83860 |
rs543221956 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7832982 | AGGAGGATGATTTGA[G/T]GCCAGGAGTTCGAGA | 83860 |
rs543226708 | snp | A/G | 1.65982e-05 | 0.00288077 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964071 | TAGTCCTGAAGCTGA[A/G]GAACTGCCAGCCATG | 83860 |
rs543231235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871513 | CAATGGTGTGATCTC[C/T]GCTCATTGCAATCTC | 83860 |
rs543231527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8002202 | AACTGAAAACGCCTG[A/G]GTTGTCCTCACACTT | 83860 |
rs543241173 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966930 | TTAACAAGACACAGA[A/G]ATCCAACTCTTATTT | 83860 |
rs543242827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7995556 | GAGATTTTATGATTC[A/G]GAACATTTGACAATA | 83860 |
rs543255317 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993170 | AATCCACACTCCTAC[A/G]CTCCTCCTCCTTTTT | 83860 |
rs543257232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845447 | ATTTGCTGGGCAGTG[C/T]TAGGGGTAGGGGTGA | 83860 |
rs543281751 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827998 | ATTAGTTCTCGTCCC[C/G]TTTTTCTTTTCTTGC | 83860 |
rs543297089 | in-del | -/ATTAT | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7869095 | ATCTAAAGATTTCAC[-/ATTAT]ATTCTACTTATTTTA | 83860 |
rs543297402 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848831 | CTATATGCCACATTT[C/T]ATAACTCTTCTTATA | 83860 |
rs543298187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963405 | CCAGATCCTGAGGTT[A/G]GGGCCAGACCATGTG | 83860 |
rs543313301 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843252 | AGCTGGGACTACCAG[C/T]TTGCACCACCATGCC | 83860 |
rs543318829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845913 | TCTTATGGTTGAAAA[A/G]GTTTGATTTCTGAGT | 83860 |
rs543321317 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818551 | CTCTCAGGCTGGCGC[G/T]CTCCGTGCTGCTGGG | 83860 |
rs543344086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956411 | AGAATCGCTTGACCC[C/T]GGGAGGTGGAGGTTG | 83860 |
rs543350103 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818972 | CGGGGTGTGCATCCC[A/G]CACCCCGCCTCGAGA | 83860 |
rs543360949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970275 | TGAATAAACTAACTC[A/G]ATAGTCAACAGTGTT | 83860 |
rs543365694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008252 | CAGGTGCACGCCACT[G/T]CACCCGGCTAATTTT | 83860 |
rs543385768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839412 | CTACTCTATGAGAGT[A/T]GAATTCAAGACATGG | 83860 |
rs543444783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908154 | TCCTCTTGTGTGTAC[A/G]TAGACATGTACGTTT | 83860 |
rs543518625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969245 | GAGGCTAAGGCGGGA[A/G]GATAGCACCACTGCA | 83860 |
rs543521542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7986769 | AGGGATCCATAACTC[A/G]CCCCAAGCAAAGATA | 83860 |
rs543532811 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7894954 | GGTCTTGGCTCACCA[A/C]AACCTTTGCCTCCTG | 83860 |
rs543544731 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7909516 | TAAAGTGCTGCATCT[C/G]TTAACAACTTAATTT | 83860 |
rs543562910 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910879 | AGCCAGAAATAATAC[A/G]TGCTTTCTTAAGTTG | 83860 |
rs543564000 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836395 | TTCTCCTGTCTCAGC[A/C]TCCCGAGTACCTGGG | 83860 |
rs543592308 | snp | A/C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891230 | CATTTTGATATAAAG[A/C/G]AGTAATTTTCTGAGT | 83860 |
rs543601716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887494 | TTCTCTGTTTCTTTT[A/C]TTTTTCTTTCCCCAC | 83860 |
rs543614702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7921227 | CTTTACTTTGAAGTA[A/G]AAGGAAAGAGCAGTT | 83860 |
rs543621180 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7879874 | CAAATTCCAAGTATG[G/T]ATTTTATTTCCTAGT | 83860 |
rs543625659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8009811 | TATTTTTAGTAGAAA[C/T]GGTTTCACCGTGTTA | 83860 |
rs543647155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950773 | TTGGTGTCAGCTCTC[A/G]CACTATAAGGAAGTG | 83860 |
rs543669739 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8002430 | AATTACTACTTTCTG[G/T]ATCAGCTTTTGTTTC | 83860 |
rs543671342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825792 | TCTTGTGATTAATGC[C/T]GCTATGAACATCGAT | 83860 |
rs543687336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8009001 | AGAAAAGCTATTTTA[C/G]GATCATGTTTTTAAG | 83860 |
rs543714300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914147 | TGGGTACTAAGATTG[C/T]CATTAATTTGCTAGG | 83860 |
rs543724963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881542 | TTAGTATAAAATTTA[G/T]CAATGAAGCTGGAAC | 83860 |
rs543731537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819072 | GTGCCTCTTCCTTAT[C/T]CGCTAACTTCCCGCC | 83860 |
rs543740351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840169 | AGTGTTTTTTTTTTT[C/T]CGAGACGGAGTCTCA | 83860 |
rs543749396 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016720 | TAAGTGAGCAGGTCA[C/T]GCTACTGAAATCAGA | 83860 |
rs543775089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907747 | TCTGTGTCTTGAAGT[A/T]TGAAAGCTGCTATTA | 83860 |
rs543776370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7970840 | ATCTAATTGGTTTGT[A/G]CCTTTAAGGAAGGGT | 83860 |
rs543808175 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TAF3 | GRCh38.p7 | 10:7826693 | TGTAATATATGCATA[C/T]GGTTTATAAGGATGC | 83860 |
rs543840078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974774 | AAGATGGAGTGGAGC[A/G]CATTTAAAAGTGAGA | 83860 |
rs543896977 | snp | C/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819287 | TTGTCACAGGCGCTC[C/G]GTCTACCGGCCGTTT | 83860 |
rs543912279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929629 | TCAACATCCCAAAGT[C/G]CTGGGATTGCACGTG | 83860 |
rs543912505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937432 | TTCTCCTAATAACAT[A/T]TAATGTGGAACATCT | 83860 |
rs543918458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982148 | TAGTAAATGTTTTTT[A/T]TCTCACTTTCTGAAT | 83860 |
rs543940231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912805 | CTGTGGCTGTAGAAA[C/T]GCTGTTTGGCGAGGC | 83860 |
rs543942676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7861148 | TTTTTGTATGTTTAG[C/T]AGAGATTGGGTTTCA | 83860 |
rs543947258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002983 | GTCTTTTTTGTGTGG[A/T]ATTACTTTTCTTTGT | 83860 |
rs543985641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7885381 | TCCATTTATATTTCT[C/T]TTTTAGGCTTTCCTC | 83860 |
rs544015462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839513 | TTGTCCAAAGTCACA[C/T]GGCTGCGAAGTGATA | 83860 |
rs544020163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958020 | ATTAGTGTAGGAAAA[C/T]ATTTTTAAGACATTT | 83860 |
rs544020361 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945654 | GAAGGCTGTCCCAGC[A/G]GCAAGGGTGTGCCCT | 83860 |
rs544022936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012824 | AAAAGCATGTCTAGT[C/T]AGTGTGGTATTTGAA | 83860 |
rs544028282 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915710 | AGGCTGGGCGCAGTG[G/T]CTCACGCTTGTAATC | 83860 |
rs544033878 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969034 | CATGTTAATGGCCAG[G/T]TGCAGTGGCTCATGC | 83860 |
rs544055752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883869 | GGGAAGTACAAGGTA[A/G]AGGGGCTACATCTAG | 83860 |
rs544080904 | snp | A/G | 1.66266e-05 | 0.00288323 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964719 | CTGTGCTGAGCGAGA[A/G]CCAGATCCTTTCGAA | 83860 |
rs544086059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012113 | GCCTACCGAGGTCAA[A/G]GCTACAGTGAGCCAT | 83860 |
rs544098677 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823077 | ATGATTGCCCTTCTG[C/T]ACTCCAGCCTGGGCA | 83860 |
rs544110545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833809 | TCAGCTGGGTGGCCA[A/G]TTGCAGTTCTTCAGC | 83860 |
rs544143111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923586 | TTGCTGTATAGCAAA[A/G]AAACAAAACAAAACA | 83860 |
rs544198797 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | TAF3 | GRCh38.p7 | 10:7854656 | AAAGAGCCCTCTAAT[-/G]GGGGGGGCGGGGGGA | 83860 |
rs544220882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837776 | CTGAGGCTGCAGTGA[A/G]CCACTGCACTCCAGC | 83860 |
rs544240227 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7843552 | TTTAAAATACTACTT[A/T]AATGTAGTTATTCGT | 83860 |
rs544271583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919133 | AATGGGAGATTGAGT[A/G]CGACTAGGGGCCAGA | 83860 |
rs544271594 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7933823 | TCTTAAGCCTGTTCT[G/T]TGGCTATTATAATAT | 83860 |
rs544296893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7940492 | AATCCTGGATAACTC[C/T]GATAAACAACTGTAT | 83860 |
rs544300258 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839916 | GGAGAGTAGAAGTCC[C/T]AGCATACACAGATTG | 83860 |
rs544304579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7981459 | TAAATATCTCATAAT[A/G]TATTGGATCAGGTGA | 83860 |
rs544324396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7824182 | TACTCTTTAAAATCT[A/G]TTAAATTCTTTCCAA | 83860 |
rs544335498 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7863541 | CTTGAACCTCAGAGG[C/T]GGAGGTTGCAGCGAG | 83860 |
rs544343305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947993 | CTATAACTTCCTGAC[A/G]TACCTTTTATTAAAG | 83860 |
rs544359414 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904900 | TGAACCCCAATTCCC[C/T]GCACTTCCTCCACCA | 83860 |
rs544372770 | in-del | -/TT | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7880951 | TACAAAAGGATTCTC[-/TT]AGCCCAAGCATGGTG | 83860 |
rs544377862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999663 | GGTTTCACCATGTTG[G/T]CCAGGCTGGTCTCAA | 83860 |
rs544388182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953904 | AGTGAGATTCAGAGT[G/T]CACTCCATAGGTGAA | 83860 |
rs544412887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961472 | CTTTGTTCACCTGCC[A/T]TCTGCATAAAACTCT | 83860 |
rs544422782 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997940 | AGTTTATCTCACAAG[G/T]GATGAAAAATTATAT | 83860 |
rs544457523 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7968635 | TTCCTTACCACAACC[C/T]TCTAAGATAGATGCT | 83860 |
rs544471160 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7967730 | CGTATCTGACGCATA[A/C]ATGTCAGTAGATGGA | 83860 |
rs544473170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961026 | CAAGCTCAGATTTGC[A/G]TGTTCGGAAGATCAC | 83860 |
rs544477847 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886274 | TTAGACATAACCAGC[C/T]GCTCCCTAATGTTTA | 83860 |
rs544492544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7928127 | AGATCTATAAGGTGG[A/G]AGTAACAACACTGAT | 83860 |
rs544497359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7842751 | AATTCCATCATTTGT[A/G]AAATGGGAATAGTAA | 83860 |
rs544501637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7836071 | GCCTTTCTTGGGCAC[A/G]TCTTCCCTGGCTCTC | 83860 |
rs544511361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876793 | TACATTTTCTTCCAT[A/C]TATTAAAACTATTTT | 83860 |
rs544521330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7939416 | CTAGATTATCTTACA[A/G]TGTAGCCCGCCAGTT | 83860 |
rs544543361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7899650 | CTGAAGAACACAAAG[A/G]AAGAAATCAGAGGAA | 83860 |
rs544544937 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884391 | CAAAGAGCTCTGCCT[A/C]CTTTTTTTTTTTGAG | 83860 |
rs544545829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7909128 | GGAATGTGTTTGGTC[A/G]TCTAGACCAAGTGTG | 83860 |
rs544547982 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966671 | GAGCTTGGCCACAAA[A/G]TAATACCCAGTAGTT | 83860 |
rs544554384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7851810 | TTGTTTTCAAGACAG[C/G]GTCTCACTCTGGCAC | 83860 |
rs544578147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850783 | AATATTTAAGAGAGA[A/C]AAGTTTAGCTTTAGG | 83860 |
rs544586860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893169 | GACTTTAACATACAG[C/T]CTTTGAGTATTTGGG | 83860 |
rs544592662 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989443 | ATTTCACGGTGCTGA[A/G]AAACATCTGTTTGCA | 83860 |
rs544595318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948560 | ATCTTTAAATCCTGA[A/G]TTGCTTGTTTTGTGG | 83860 |
rs544607420 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934086 | TAGAGATTGATACTG[C/T]GAGGCAAGGCATGAA | 83860 |
rs544611841 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7885631 | TTGCATCTATATTCA[A/G]TTATCCATGTTTCTA | 83860 |
rs544673928 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7906231 | TTATCTTTAATTTCA[A/G]TATTGGATGGTAACA | 83860 |
rs544684497 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966588 | ACTTTCCGAAAAAGT[A/G]TCTCTTCATAGTGCC | 83860 |
rs544686658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7912837 | CTGGTGCTTTTTTTC[C/T]TTTCTGAATCGGACC | 83860 |
rs544735271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899689 | ATGTTCACAGTAAAC[A/T]TATTACTAAATAAAA | 83860 |
rs544741070 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7906861 | AAGCTGGGACTGCAG[G/T]CGTGCACCACCATGC | 83860 |
rs544742306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928710 | TGTCATTCTACTCAC[A/G]ATGATCTAGGTAATG | 83860 |
rs544743964 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992505 | AGTTCAAGGTGATTA[C/T]TCCCAACTAGGAAGG | 83860 |
rs544750872 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956461 | CACTGCACTCCAGCC[-/T]GGGCAACAGAGTGAG | 83860 |
rs544760543 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894361 | TATTATACAGAACAT[C/G]AAAATCCATCAAGTA | 83860 |
rs544769577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976809 | TTTCTCATTTGATAA[C/T]GCAAACTTAAGATGA | 83860 |
rs544788783 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7884668 | GCTGGGATTACAGGC[A/G]TGCGCCGCTGCGCCT | 83860 |
rs544793682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864088 | CCTTGACACATTATT[A/G]TTACCAGAGTCTGTA | 83860 |
rs544794012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857350 | GTACATAGTTTTATC[C/T]GATTAGCAAGTTAGA | 83860 |
rs544816820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006718 | ATCAGAATAGCAAAG[A/T]GTCAGTGCCTTTTGG | 83860 |
rs544834890 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893903 | CATCCTTCTCAAAAG[A/T]CCCCTTAAGAAACAC | 83860 |
rs544847683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877695 | GATTACAACCCTACT[A/G]TTTAAAAAATAAGAC | 83860 |
rs544854630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858039 | CAGCTTACAAAGAGG[G/T]TTGAACGGCCTCAGT | 83860 |
rs544874516 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7845236 | GTTGAAATGTGGGAA[-/C]TACCAAAAAAAAAAA | 83860 |
rs544934876 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915909 | CTTGAATCTGGGAGG[C/T]AGAGAGTGCAGTGAG | 83860 |
rs544949897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7892452 | AAACATAGTCAAAAA[A/G]CAATTGAAAACTTGC | 83860 |
rs544997514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961563 | TCTTTTTATATATAG[A/G]TATTCCTCAAAATAC | 83860 |
rs545021203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919197 | CCTAGGAGGCCTAGC[C/T]TCTGGCTAAGGTAAT | 83860 |
rs545024783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832564 | TATTTATTTATTTTT[A/G]AGACAGTCTCGCACT | 83860 |
rs545034470 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861395 | ACAAGCATGAGCCAC[C/T]GCACCCAGCCAACAG | 83860 |
rs545035397 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7838280 | TCTCTCCCCATTTTG[A/G]CCTTTCTGCTGTTGT | 83860 |
rs545039494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927104 | AAGCACTGGTCATGC[C/T]CAAGTATTGTTGGAG | 83860 |
rs545054773 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963843 | AGAAATCATATTTGA[A/G]GCATTGTTTTTATTT | 83860 |
rs545058713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913434 | TTTTTCTATGCCCTT[G/T]TCTCATAAGTAATAG | 83860 |
rs545078913 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7935544 | AGCCGAGATCGCGCC[A/T]CTGCACTCCAGCCTG | 83860 |
rs545080714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7921519 | CAGTTTAGTGAGTTG[A/G]AACTAGCATTTTAAA | 83860 |
rs545094459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864589 | AGGTTTCTGTGTAGA[C/G]TCGTGTTTTCATTTT | 83860 |
rs545099178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974842 | GCACTTTGGGAGGTC[A/G]AGGCGGGCGGATCAC | 83860 |
rs545103857 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7934710 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGTG | 83860 |
rs545104151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926821 | ATAGTTTTTAAACTT[G/T]GCTGCTATTTAATCA | 83860 |
rs545118240 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7858111 | CATGAAATCATATTG[C/T]TTCCTCTTATATCCC | 83860 |
rs545139294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942028 | GTTTTGAGGTCAGTT[C/T]TTTTGCTTCACAAGT | 83860 |
rs545144261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7922404 | TAATCTCATTCCTCA[A/G]TTTCTCCAAGCCTCT | 83860 |
rs545148329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825922 | TTTGAGGAAGCACCA[A/C]ACTGTTTTCCACAGT | 83860 |
rs545165476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934304 | CAGAATTTAATTGGC[A/G]GGAGTTTTTTCGTTA | 83860 |
rs545206594 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909645 | TGATAGCAATGAATC[C/T]AGGGCAAAAGGAAAC | 83860 |
rs545214402 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7954862 | TCAGAGTGCACTCCA[C/T]AGGTGAATGAGTGAA | 83860 |
rs545216791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914215 | TACCTTTTCTATTAG[A/G]AATACGTATGGAATT | 83860 |
rs545235685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885311 | TAATTCCTTCCCCTA[A/C]CCCCAGTGTAGTTAG | 83860 |
rs545249987 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7961951 | ACCTTCTGGGCTCAG[G/T]TGACCCTTGCACCTC | 83860 |
rs545258127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962885 | TTAGACTTTATCATT[G/T]TACATTATATGCTTA | 83860 |
rs545270894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918860 | TTTACTGCAAGGAGG[A/G]ATAGCAGGTGGAAGG | 83860 |
rs545274999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837618 | AGTGTACTCCAGCCT[A/G]GGCAAAAGAGCAAGA | 83860 |
rs545277138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7928742 | CCTAAGACTGGGGCC[C/G]TTTCTCTTATCAAGT | 83860 |
rs545283910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7954504 | AGCTCTCCATAGTGA[A/G]ATTCAGAGTGCACTC | 83860 |
rs545362894 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864384 | ATATAGGCACTGTGG[A/G]ATGGTTAACTCTAAC | 83860 |
rs545369053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886870 | CTTGAATTGGAAAAA[A/T]TTTAAATACCATCTC | 83860 |
rs545370156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823778 | TAGCTGGGATTACAG[A/G]CCTGCGCCACCACGC | 83860 |
rs545373623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7844504 | GCCTCAGCCTCCTGA[G/T]TAGTTGGGATTACAG | 83860 |
rs545380775 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913568 | AACTCACCACCCAAT[C/G]TGGCAAACCTATCTG | 83860 |
rs545386490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984743 | AGGAAAGTACTTAAG[A/G]TTCATTATCTAGAAA | 83860 |
rs545397936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886283 | ACCAGCCGCTCCCTA[A/T]TGTTTACCAAGTGTT | 83860 |
rs545405268 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7911931 | TTCTGGTTCCTAAAG[A/G]CACTTAAGTTTAAAG | 83860 |
rs545408972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839060 | ATAAACCTACAGGGC[C/T]CTGTGTGATCGGACT | 83860 |
rs545418053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834921 | TCTGCTACCTAATTT[A/C]TGAGTTTTTTCTGAT | 83860 |
rs545437266 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849231 | GATAACTTTTAAGGT[A/G]TGTTAGAAACTGGTA | 83860 |
rs545439206 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7847799 | TGAGACAAGAGTTTC[A/G]CTCTGTCTTCCAGGC | 83860 |
rs545445989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984167 | GAAAAGGAGTTTTTG[A/G]CTTCCTTATATTACT | 83860 |
rs545464578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879950 | ACGATGGGTCACAAC[A/G]GTAATCCTGGCAACT | 83860 |
rs545469429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832993 | TTGAGGCCAGGAGTT[C/G]GAGATAAAATGTTCA | 83860 |
rs545527578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7872259 | CAGTAGCTACCCGCT[C/T]CTCCGCCTTTGCAGT | 83860 |
rs545539508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829250 | TCACTCACATCTGAA[A/C]CATTTCTTCTGTTAT | 83860 |
rs545547926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7948769 | AATTTATCACTGGGT[A/G]CTGAACTAATGTTTA | 83860 |
rs545554551 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7858824 | TGTGTGTGTGTGTGT[A/G]TGTGCGCGCGCCTGC | 83860 |
rs545565380 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883226 | CTCTTTAGTTCTTCA[A/G]TCTAGAACAGTTCCT | 83860 |
rs545572802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7851090 | AGTAAATTCTATAGT[A/G]TGTTTGGAAGAGGAT | 83860 |
rs545592417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903252 | CCATTTCTGTCATCA[C/T]GTATGCTGCTGCTCA | 83860 |
rs545611522 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855942 | GAAAAAAAAAAAGAC[-/A]AAAAAAAAATAAGCG | 83860 |
rs545671567 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961035 | ATTTGCGTGTTCGGA[A/G]GATCACCGTAAGACG | 83860 |
rs545704056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893826 | TAGGATCCTTCTTAC[A/C]TAAATTGATCCTCTT | 83860 |
rs545726057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7977036 | CCATATTTATATAGC[A/G]TGATTAAAGTTTGCA | 83860 |
rs545726672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935977 | TCTCATTTGGGCTGC[C/T]GATTGTAGGGGCTCA | 83860 |
rs545733478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931610 | AAAAGCAAGAAAATG[G/T]TAATTATACCTTGAA | 83860 |
rs545733806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7938640 | TGAAATGATAGTGAA[A/G]TAGTCAAGCCAAGAT | 83860 |
rs545745129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7841003 | TACAGGCACACGCTG[C/T]CACACCTGGCTAATT | 83860 |
rs545764680 | in-del | -/AA | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7953570 | GGTGTCATTTCAGTT[-/AA]AGGTTCCCTGCCCAG | 83860 |
rs545782676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952997 | TATGATTGTTTTTGA[C/T]GCCATGCCCTTCTTT | 83860 |
rs545797574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882445 | AAAAGGAATCTTCAG[A/C]AGTAAGAAATGAGAG | 83860 |
rs545800678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897025 | GACATTCTTGACCAC[A/G]TGGTCCCTCCATCCT | 83860 |
rs545828006 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7857084 | GAATATAGTTCCAAC[A/G]TGAATGTTGGTTGAT | 83860 |
rs545851091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945168 | CTGGCACCCGTGGCA[A/T]TAGAGGACTGGATTG | 83860 |
rs545867636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925146 | AACCTTGGGATAAAA[A/G]TCTATTTTTAAACTT | 83860 |
rs545868786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883142 | GTGATACCCTCCGTA[A/G]CAAAAGGAAAGGACA | 83860 |
rs545931033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917307 | GGCATTGAAGCAAAT[C/T]GAAGGGAAGAAGTCC | 83860 |
rs545932092 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7875948 | CTCCAAACAAGTGAT[A/C]GTAATCTTATATTAC | 83860 |
rs545932939 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880140 | GCTACTCAGGAGGCT[A/G]AGGTGGGAGAATCAC | 83860 |
rs545937755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898931 | CATGCGTACTGTCAG[C/G]GATGGCAAGTGGTGC | 83860 |
rs545951861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982376 | AAAAAAATACATTTT[A/T]AAAATTAATTTGTTT | 83860 |
rs545954943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7965900 | ATTTGATTTTAATTC[G/T]AAAACCCATAAACCT | 83860 |
rs545989321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854426 | ACACACATGGAAGCT[C/G]TATGTGATTTTTGGC | 83860 |
rs545994798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966419 | GACTTCATTTCATAG[C/T]ATACAGCCCGACAAA | 83860 |
rs546002792 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891333 | ACATAGTAAAAGACA[C/G/T]AGATACAAGTTAAAT | 83860 |
rs546025714 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958962 | ACATGGTAAAACCCC[A/G]TCTCTACTAAAAATA | 83860 |
rs546041956 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878167 | GTACCCAGGAGCAGA[C/T]CCTGATTTTGTGAGG | 83860 |
rs546091961 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876409 | GTATTTTCAATGAAA[C/T]GGGCCATAAGCAGGT | 83860 |
rs546105786 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | TAF3 | GRCh38.p7 | 10:7990383 | ACCTTTTTATTGTTT[C/G/T]TGTCATTTTGTTTAT | 83860 |
rs546114974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953839 | AGACTCAAGAGTGCA[C/T]GCCATAGGCAAATGA | 83860 |
rs546115577 | in-del | -/CAGATGTCAGCCCAGTCGAGCC | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7896851 | TAACAAGGCCAAAGT[-/CAGATGTCAGCCCAGTCGAGCC]CAGATGTCAGCCCAG | 83860 |
rs546124281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868936 | GGTTTAAACTTATGA[A/C]GGTCTGACTCCAGAA | 83860 |
rs546134929 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945850 | CCTAGCACTTACTGT[G/T]AATTTTCCTTTTGTA | 83860 |
rs546143794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916673 | TGTAGATCAAATCCC[A/G]GCTTAACTGCTTTAG | 83860 |
rs546152484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822829 | TAAAGATGTAGAGAC[C/T]TTAAGCTCTGCTAAG | 83860 |
rs546167176 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7998787 | GAGGTTGCAGTGAGC[C/T]GGGATCGCGCCACTG | 83860 |
rs546170966 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7907988 | TCAGTTCAGGAGATA[C/T]GTAGAAGAAGTTGGC | 83860 |
rs546179943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7978685 | ACCCAACCAAAGTAA[A/G]TCTTCCATCTCCATG | 83860 |
rs546187174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862905 | GTATTGTTCCATTAC[G/T]TGTATATGCCACAAT | 83860 |
rs546190867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821682 | TTAAATATGTTGGCA[A/T]GTACTGAAAGCAGGT | 83860 |
rs546219009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905270 | AACAGAAGAGTGACA[C/T]GCGCTGCCTTGACTA | 83860 |
rs546242605 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003958 | TATTTTCATAAAAAA[A/G]AATGTTATCTGTTAA | 83860 |
rs546261693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981780 | ACATGTCATTTACTT[A/T]TTTTTGTTGCATTTC | 83860 |
rs546274868 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959659 | GAGCTCTAAATTCAA[A/C]GTAAACCAATATATT | 83860 |
rs546284971 | in-del | -/ACAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006222 | CACACACACACACAC[-/ACAA]ATTAGCTGGGCGTGG | 83860 |
rs546334454 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939793 | AGATAAAGAGAGGAA[C/T]GATAGGAGAGAAAAA | 83860 |
rs546358838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910767 | GGCTACTAACTAAAA[A/G]ACAGGAATAATTCGG | 83860 |
rs546359242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868143 | AAGGGGGCATGTGTA[A/G]TTCAAAGCCATGTTG | 83860 |
rs546378936 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7862634 | TGAAGATATCCATCA[C/G]CCTGAAAAGTTACCT | 83860 |
rs546387569 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7822339 | TATGGAGGAATTTAA[A/G]ATTATTATATTTTTT | 83860 |
rs546400957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876604 | TCCTGTAGGTGAGCA[C/T]CGTATACAGAATCAC | 83860 |
rs546411629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938357 | GGTTATCAGGCTGTT[A/G]TATTTTAGTTCAGGG | 83860 |
rs546417091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923848 | TTAATACAGAAAGCA[A/C]GGCAAGATATCTTAA | 83860 |
rs546420139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904312 | CCTCCCTAACCAAGC[A/T]AGACTGGTTCCTTTC | 83860 |
rs546437357 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7951654 | TGGAAGGGCATAGAT[C/G]CAGGGAGGGGAAGAA | 83860 |
rs546466147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7827802 | AAAAAAAAAACAAAA[A/G]CAAAAACTTAGCTGG | 83860 |
rs546482045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924536 | TGCACATCTTTATGT[A/G]GGCATGTCTCCCATT | 83860 |
rs546487330 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7925933 | CTTAAGACTGGTAAG[A/G]CCAGGTGCAGTGGCT | 83860 |
rs546492880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7911282 | TTATATTTAGTCAGT[C/T]AGTGAAATCTGGCCT | 83860 |
rs546506197 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7946515 | GATTATTTGAGCTCA[G/T]AAGTTTGAGACCAGC | 83860 |
rs546524191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7959841 | TCCAAATTTTCAAGT[G/T]ATTGTAACTATAAAG | 83860 |
rs546538723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882635 | AGGAAGAATTCTCCA[A/G]CAGTCAGTGTCTAAA | 83860 |
rs546545100 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965355 | GAAGGAGAAAGAGAA[A/G]CATAAAGATAAGAAG | 83860 |
rs546545501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842321 | TGCACCACCACACTC[A/G]ACTAATTTTTTAATT | 83860 |
rs546554808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7835032 | TTCTCTCGTACTTTC[A/G]TTGTCTGGAGGGATG | 83860 |
rs546556540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904725 | TGTGCACAGCGTTGG[C/T]TTTCATGATATTTAG | 83860 |
rs546564930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010751 | ATCTCTACTAAAAAT[A/G]CAAACAAAATTAGCT | 83860 |
rs546574678 | in-del | -/GTG | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7923269 | TTAAAAAATAGAGTA[-/GTG]GTAAGAACAGGGTGT | 83860 |
rs546578034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829428 | ATTGTGTTTGGTTGT[A/C]ACGTCTCCTTAGACT | 83860 |
rs546606034 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934827 | TGCGATCAGTTTACT[A/G]ACTAATCTATTCATT | 83860 |
rs546649998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946558 | GCCAAACCTCGTCTG[A/T]ATGAAAATACAAAAA | 83860 |
rs546655302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903669 | AGAATTATAGAAGCA[C/T]GATTTTCAGGAGACT | 83860 |
rs546677900 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7855507 | CTTTGGGGAGGAGAT[A/T]TGAGATTTCTCTAGG | 83860 |
rs546708692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7930893 | TGTAGCACCTATAAG[A/G]TGTTACTATCTCTAG | 83860 |
rs546709975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7989513 | CTGTTTTAAATTTCC[C/T]ATGAAATACGTTTTT | 83860 |
rs546711642 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7980001 | CATTCAAATTTCAGT[A/G]ATCCTCCGTGGTTGT | 83860 |
rs546713535 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7971457 | CATATATGGTGTTTT[G/T]TTTTTTTTTTAATGA | 83860 |
rs546720105 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836131 | TTTTATCCTTCACCT[A/G]CTATGTTTCTCACGT | 83860 |
rs546728352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876998 | TGAACTTCCTTTACT[C/G]AAATTGCCCACTTTC | 83860 |
rs546730445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840644 | GAGGGGAAGACGGGA[A/G]TATCAAGGAGGAGCA | 83860 |
rs546744452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949160 | TCTGTGCGTGCACAG[A/G]TGAAGAACCTTGTGC | 83860 |
rs546774406 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7996959 | TCAGCCTCCCAAAGT[C/G]CTGGGATTATAAGCA | 83860 |
rs546775986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980036 | TGATACATGGCTTAG[A/T]CCATGGTGATAATGG | 83860 |
rs546787271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834564 | TGTAGATGTGTGTGA[A/G]TAGATAGATAGGTGG | 83860 |
rs546829806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841094 | GACCTCAGGTGATCC[A/G]CCCACCTCGGCCTAC | 83860 |
rs546833269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966701 | TTTGTTCATATGATA[A/C]AATTTGATGTATTTG | 83860 |
rs546833418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974903 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 83860 |
rs546835969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004200 | GGATTACAGGTCTGC[A/G]CCATCACACCCAGCT | 83860 |
rs546844854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856292 | ACCAGCCTGGCCAGC[A/G]TGGTGAAACCCCGTC | 83860 |
rs546868294 | in-del | -/A | 0.198324 | 0.244601 | intron-variant | TAF3 | GRCh38.p7 | 10:7915643 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 83860 |
rs546878713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7874864 | ACACATAAACTAAAG[A/C]AATTATGTATTGAGC | 83860 |
rs546882268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7842043 | GTTGGCCAGGCACCA[C/T]GCCCGATGTGGGAGG | 83860 |
rs546922306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010208 | AACCATGCCCAGCCA[A/G]GATGCATTTCTTCAT | 83860 |
rs546942393 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906947 | CTAACAGCGTGATTC[A/T]TATCTAAGACTTTGC | 83860 |
rs546971052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7932926 | CTCGAGTGATCCTCC[C/T]GCCTTGGCCTCCCAA | 83860 |
rs546995015 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000220 | CTCCTGGGTTCAAGC[A/G]ATTCTCTAGCCTCAG | 83860 |
rs547005345 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7981108 | TGTGAGAAAAAGGTG[A/T]AACACTGGTAAAGTA | 83860 |
rs547007201 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7984398 | TTTCCATCTTACTTG[A/T]AAACAATTACAGCAG | 83860 |
rs547023907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884679 | AGGCGTGCGCCGCTG[C/T]GCCTGGCCTGCCTCC | 83860 |
rs547029247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7838744 | CCCCCTAACATCCGA[C/T]GCTATAAGCCTCCTC | 83860 |
rs547033707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7939378 | TCCCAGGGAAAATAC[A/G]TACTGACAATAACAT | 83860 |
rs547066177 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7988936 | ATATAAATATCACAG[C/T]AAAAATTTTTTCTGT | 83860 |
rs547068158 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882435 | CAGGGATGAGAAAAG[A/G]AATCTTCAGAAGTAA | 83860 |
rs547105838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918246 | GGTTTGAAGAGAGAC[A/G]AGAATGTATGAAATG | 83860 |
rs547111943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998023 | TTTTAAAACTGTTTT[C/T]GGTCATCACAAAAAT | 83860 |
rs547114281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7872609 | GCCATAGTTATAATA[C/T]CTTGCTTTCAGGTGC | 83860 |
rs547151976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960706 | GAGGGAGCACCTTGT[C/T]AGTCATACTGGAGAA | 83860 |
rs547155992 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7992452 | TAGACGGTAGGAAGT[G/T]TTAAAGGCTGGAAGA | 83860 |
rs547156730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823274 | GATGCATCAGGGAAC[A/G]ACAGAGGAAATGTAA | 83860 |
rs547178787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011699 | TCACCCCCAAATGGG[C/T]TGATCAGGAAAGATT | 83860 |
rs547179427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7834259 | CTTTTGGGGCCAAAT[A/G]TAAAAAATAATTGCC | 83860 |
rs547185044 | in-del | -/CA | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7871970 | CACGTTTCTGAAATT[-/CA]CAGTTATTTCAAAAC | 83860 |
rs547197215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856622 | GTGACACTGAGGACC[A/C]ATAAAGCCAGATTGT | 83860 |
rs547198459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880887 | TCTGCTAATCCAGCA[C/T]ATCTGTGTTTAGAGG | 83860 |
rs547217672 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870266 | AATTCTCATCAGTCA[C/T]TGGTTGTACTTTGGA | 83860 |
rs547222741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978389 | CCAGCATGATTCTGA[G/T]GAATGTGAGCAGAGA | 83860 |
rs547244240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963185 | TTGTCATAAAAGTCC[A/T]AAAAATACCTGTCAT | 83860 |
rs547278975 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854805 | ATCAGTAGTATGTTA[C/T]AGTAGCATGGAAGCC | 83860 |
rs547284353 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949292 | ACAGCCGGAAATAAA[A/G]AGTGGGCTGCTTAGC | 83860 |
rs547284577 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014989 | GAGGCGTGGCCTGGG[A/G]GCTGCCCCTCCTCCA | 83860 |
rs547287512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926307 | GTGGATTGGCCACTA[C/T]GATGTTGTACATTTT | 83860 |
rs547321212 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818300 | CTCTAAAACACTGGC[A/G]TTTTCGTCACCGCTG | 83860 |
rs547344930 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973668 | GGGAATATAACCAAG[C/T]ACAATGCCTGGCAAA | 83860 |
rs547346877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893616 | ATCTTTTTCACTCCC[A/G]TAGCGAGATCCGTCC | 83860 |
rs547367129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7887085 | CTAAAAATAAAAAAA[A/T]TTAGCCGGGCGTGGT | 83860 |
rs547389495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7895488 | GCATCACACTTTCTT[A/G]CTGACATCATGGTCC | 83860 |
rs547389970 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872543 | GCAAATTACTCAATG[A/G]GGAACGTTTAAAACT | 83860 |
rs547398550 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000532 | AGCACTTTGGGAGGC[C/T]GAGATGGGAGGATCA | 83860 |
rs547409403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886650 | AAATAACATATATAC[A/G]TCATAGCACATAGCT | 83860 |
rs547409601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8001840 | AATTGCACATGCGTA[A/T]TTATTGCATAGTAAA | 83860 |
rs547439693 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861187 | GCCAGGGTGGTCTCG[A/G/T]TCTCCTGACCTCGTG | 83860 |
rs547444453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833441 | GTTTTATTTCTGTAA[C/T]GATTAGTAATGTTGA | 83860 |
rs547451932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895933 | GCCTTCAGTGAACAC[C/T]GAAGCTGACCATGCG | 83860 |
rs547457087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957526 | AATTTTCAGAATACT[C/G]TCAAGATAAATGGTG | 83860 |
rs547468739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8008721 | CCCTGTCAGGCCCCC[C/G]CGAGGACTCAGCAGA | 83860 |
rs547494091 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:8000904 | TTGTTTGCTTTTTTT[A/T]TTTTCTTAGAAAAAT | 83860 |
rs547537560 | in-del | -/A | 0.499902 | 0.00698814 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817857 | TTACCTGTTTTTTTT[-/A]AAAAAAAAAAAAAAA | 83860 |
rs547552137 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7898771 | GAGAATATTGTGTTG[-/T]TTTTTTGAAACTGTC | 83860 |
rs547561697 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962171 | CAAAGCTTTGAAATT[A/G]TGTTTGAGTCCTTGC | 83860 |
rs547564789 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951662 | CATAGATGCAGGGAG[G/T]GGAAGAATGTCTGTT | 83860 |
rs547578389 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976564 | GGACTACAGGCGCCC[A/G]CCACCACGCCCAGCT | 83860 |
rs547622631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900512 | AACCACTATTGTGTG[A/G]TCCTGAAAGGAGCCA | 83860 |
rs547646727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7831387 | GTCTCACTCCATCGC[C/T]GAGGCTGGAGTGCAG | 83860 |
rs547652882 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7865474 | ACAGAGTGAGACTCC[A/G]TCTCAAACAAACAAA | 83860 |
rs547670811 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934743 | AGCCACTGCACCCCA[A/C]CTCCCTTCCTTTAAT | 83860 |
rs547685223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929148 | AATATTAGAAAATGT[C/T]TTATACAAAGACAGG | 83860 |
rs547704445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936311 | ACTAGGCATTGTGGG[G/T]TCTGTCAAAAGCTAT | 83860 |
rs547736511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839705 | TTATTTTTTTTTTAA[C/T]TGTGTTTTGTTAACA | 83860 |
rs547763524 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969472 | AAAATTTTGGTTTCT[G/T]TGTGGGTTGGTGTAT | 83860 |
rs547799883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950278 | AGAGATAGAGAAATA[C/T]AGAACGACCCAGGGA | 83860 |
rs547815436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956824 | ACATTTTAGTGACTG[C/T]GTGAAAAACATGAAA | 83860 |
rs547830518 | in-del | -/AAAAAAAAAAAAAAAA | 0.49706 | 0.0382258 | intron-variant | TAF3 | GRCh38.p7 | 10:7988573 | GTGAGACCCTGTCTC[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 83860 |
rs547837820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7846149 | GTTTTGGTAGAGATG[A/G]GGTTTCACCGTGTTA | 83860 |
rs547846431 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7943608 | GCTTGAAGAATAAAT[A/T]CTTGTCATTTCCTCT | 83860 |
rs547876408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963619 | CAGTGAGAACACATG[A/G]ACACAGAGGGAGGGG | 83860 |
rs547877509 | in-del | -/TTTTA | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7875971 | ATATTACTATTAAAC[-/TTTTA]TTTTATTTTATTTAT | 83860 |
rs547899440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846554 | CTATTACAGTTTTGA[A/G]TGGTTTTGACTAGTT | 83860 |
rs547903915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865940 | CTTCATCCTCCCCAT[C/T]GTGTGTAACAGACTG | 83860 |
rs547904441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7977582 | CCTGACATTATTTCT[A/G]CATAGTCTTTAAGGT | 83860 |
rs547919075 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016221 | GATCTGTTGGATGCT[A/G]GAATATGGGCTTTGA | 83860 |
rs547941967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936360 | GCTTCTAGTTGGGGA[A/G]ATAAGACGGGGATTT | 83860 |
rs547963507 | snp | A/G | 1.72782e-05 | 0.00293918 | missense | TAF3 | GRCh38.p7 | 10:7964484 | GTCCCAAGAGCCCCA[A/G]GGTCACGACTCACAT | 83860 |
rs547964874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7923667 | CAATAGAGTAGCGGA[C/T]ACCTGATGGCAAAAC | 83860 |
rs547966366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922743 | AGTTTTACATACTGG[A/T]ACGTATAAAAGGTAT | 83860 |
rs547968116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979162 | ATCCTGTCTAACACG[A/G]TGAAACCCCTTCTCT | 83860 |
rs547968689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937826 | TTAGCTAGAAAAGGG[A/G]TACTTTTTTTATGCT | 83860 |
rs548008420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950021 | ATACATGGTGAAATC[A/G]TTTCTCTCATTTTTC | 83860 |
rs548009107 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7865838 | CCTATCCATTTCCTT[C/T]CTTTCTGCTCCTTCT | 83860 |
rs548010260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826775 | ATAAGAAAAGGATAT[A/G]AAATGCAATTCTTTG | 83860 |
rs548012142 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819576 | CTGGGCTACAGTACT[A/T]ATGAGTTTTAAATGA | 83860 |
rs548023946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7963665 | CACCTGTTGGGAGGT[C/T]GGGGGCTGGGGGAGG | 83860 |
rs548065170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995477 | TATCTTTCTAGTGTA[A/T]CTCATTGCAAATATG | 83860 |
rs548070525 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7846085 | TGCCTCAGCCTCCCA[A/C]GTAGCTGGGACTACA | 83860 |
rs548071188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944513 | GTAACCCAAATGTAG[A/G]TTTGCAACGTTAAAG | 83860 |
rs548075275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839256 | CCCGTATAATATATA[C/T]CTCTACCATCATACT | 83860 |
rs548084142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902035 | GGCAGACACTAACTC[C/T]GCACCCCACGTTCGT | 83860 |
rs548092509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008764 | GAGCGCCACCTCTGA[A/T]GCCGTCAGAGCTTCT | 83860 |
rs548133559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950989 | AGTGCTGTGCACTGG[A/G]AGTTCAATGTTAATG | 83860 |
rs548134027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978423 | AACTTGGTTTTCCAG[A/G]GGAGTGTATACCCCT | 83860 |
rs548135963 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830733 | AAGTGATCCGCCAGC[C/T]TCGGCCTCCCAAAGT | 83860 |
rs548140528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996059 | TAAGTTAGAAAAATC[A/G]AACACCTGGTGTGTT | 83860 |
rs548152800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7917929 | AGACCGAGGAGAGGA[A/G]TGGAAGGTAGGAAGG | 83860 |
rs548158394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7881140 | ACTTGGGAGGCTGAG[A/G]CAGGAGGATCACTTG | 83860 |
rs548185770 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7833947 | ATCTTGCCATTCCCG[C/T]TGGGCACCATGGCTG | 83860 |
rs548190333 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890886 | CTTTTTACATTCATA[A/T]TTCCTTGGTTAATAT | 83860 |
rs548208545 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002659 | AAGAATGAATATTCC[A/G]CACTGATTGAAGACA | 83860 |
rs548220777 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7873623 | TCCGAGTTCTCCCCC[C/G]CCCCCCGTCAAAAGG | 83860 |
rs548248631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826938 | GTGAACCCCTTTGAT[A/G]ATGATGCTGTTCACC | 83860 |
rs548257994 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000653 | GCATGGTGGCACGCA[C/T]CTGTAGTCCCAGCTA | 83860 |
rs548278821 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919586 | GAGCATTGGTTCCAG[A/G]ACCCCCCATAGAGAA | 83860 |
rs548280731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951542 | CAGCCGCTTTCCATG[A/C]CTCTGCTTCTGTCAC | 83860 |
rs548295560 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7915114 | CCCAGCTACTTTTTT[C/G]TATTTTTAGTAGAGA | 83860 |
rs548296919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896575 | ATTCGACAGTCGCAT[C/T]TGGGGACAGATTTAG | 83860 |
rs548304113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994478 | GAGTTTATACTGTTT[C/G]CAGTTCAGATTTAAT | 83860 |
rs548304810 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946584 | AAAAATTATCCAGGC[A/G]TAGTAGCACATGTCC | 83860 |
rs548328625 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7847484 | GAGTCTTGCCCTGTC[G/T]TACAGGCTGGAGCGC | 83860 |
rs548339143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853025 | TTATTATCCATTGAT[A/G]TTCAAATTGTCCCAT | 83860 |
rs548348496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820081 | ACCACGCTGAGCTAC[A/C]TGCCTTTTCCAAAAT | 83860 |
rs548366206 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928295 | TGATACCTAGTGCCA[C/T]ATAGGAAGTACTTAA | 83860 |
rs548380137 | in-del | -/AAGA | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7837709 | AGGCTGAGGTGGTGT[-/AAGA]AAGTACTCAGAGGCT | 83860 |
rs548405582 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7954701 | AACACAGAGCTCTCC[A/C]TAGTGAGATTCAGAG | 83860 |
rs548410002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894380 | ATCCATCAAGTACTC[A/G]TTGCCTGCATTACGT | 83860 |
rs548413867 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016968 | CAGAGCCTTTCACCT[C/G]TAGGTCAGTGAGTCG | 83860 |
rs548421438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861243 | GCTGGGATTACAGGC[C/G]TGAGCCACCGCATCC | 83860 |
rs548468848 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979397 | TGATAGTTATATTCA[A/G]CTCACCTGCCTTTAA | 83860 |
rs548472650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7895117 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 83860 |
rs548474900 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016347 | TGGTTAGAGAAATGC[A/G]GTTTTCTGCCATGAA | 83860 |
rs548482409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7861630 | ATATTTTTCCACCAT[C/T]TCATAACCTCCATTG | 83860 |
rs548501262 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7929840 | AAAAAAATGTCCAGG[A/C]ATGACAAGAAAAGAG | 83860 |
rs548527800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999747 | CAGGCGTGAGCCACC[A/G]TGCCCAGCCCAAATG | 83860 |
rs548570173 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7891905 | TAAATGGAGTATCTA[C/T]TTTGCTTGTTAACTC | 83860 |
rs548588077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006119 | CAGATGACCTGAAGT[C/T]GGGAGTTTGAGACCA | 83860 |
rs548591013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7944619 | TACCATAGTTATTGA[A/G]TAATTACTCAAATAA | 83860 |
rs548627140 | in-del | -/TTTT | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8003911 | AAACATTGCCAGTCA[-/TTTT]TTACCAAGTTTTTTG | 83860 |
rs548632425 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7892705 | ACAGTATTTTTGGTT[A/G]GTCAGCCAGTTAGTT | 83860 |
rs548649775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002618 | AAATTGGGTCAGTTT[A/C]TTTCATTGTTCAGTA | 83860 |
rs548666477 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7850399 | TACTATTTAAGGCTG[A/G]GAGCAGTGGCTCATG | 83860 |
rs548695693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7893381 | ATCACTTAAAAGATA[C/T]GTTGCTTTTAGGATC | 83860 |
rs548695866 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914878 | TATGATAAACACATC[A/T]GACCACATGTGCCTG | 83860 |
rs548697358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7841147 | TGAGCTGCCGCGCCC[A/G]GCCTAGAGCTTTCCT | 83860 |
rs548727719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972537 | AGATGATACAAACAC[G/T]GTAATTACAGATGAA | 83860 |
rs548742481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869925 | TGCCTCTTTTATCAC[A/G]CCTGACCCCTGGGTT | 83860 |
rs548750862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954064 | AGGCGAATGAGTGAA[G/T]TAGTTCTAGTTAACA | 83860 |
rs548751835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7872756 | TTTCACGCTGCCTTA[A/G]AATCATACAATTTTG | 83860 |
rs548752793 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997730 | TTTCTCTGTGAGACA[C/T]TGCTTATTCAACAGA | 83860 |
rs548764360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931875 | TCTTTGGCCTCATGG[A/T]TAAGACAAAAACAGA | 83860 |
rs548767498 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995100 | ACCACTATCACTACT[A/G]CCACCAAGATTATTA | 83860 |
rs548778835 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922579 | GAATAAAAGCATGAC[A/G]TGTTGAGATGACTGC | 83860 |
rs548789431 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843738 | ACACATACAATTAAC[A/G]TGCATTAATTGATTA | 83860 |
rs548799653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980075 | GTGACAGATTCCTGT[C/T]ACTGTGCCTGTGGTT | 83860 |
rs548802931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7863731 | TATACACATATATAT[A/G]TACACATATATATAT | 83860 |
rs548805397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820606 | CTCAAGTGATCCTCC[C/T]GCCTCAGCCTTCCAA | 83860 |
rs548815571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909238 | CAGAGCCTCTGGGGC[C/G]CAGGCTCTGGGTTTC | 83860 |
rs548862968 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877639 | TATCATTATCTTGTA[G/T]TAAGAGAATTTAAGA | 83860 |
rs548909558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899382 | ACATTCAGCAAGTCC[C/T]ATGTCCATCTTCCCA | 83860 |
rs548919550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913817 | CCAAATACATTGAAC[C/G]TGAAGTGCAGTCAAG | 83860 |
rs548920697 | in-del | -/AAAGAT | 0.00041731 | 0.0144389 | cds-indel | TAF3 | GRCh38.p7 | 10:7965392 | AGAGAGAAAGGCAAG[-/AAAGAT]AAAGATAAGAGAGAG | 83860 |
rs548922266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990835 | AGCCCTTATCCCATA[G/T]ACCTCCTCACAGAAG | 83860 |
rs548925399 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896317 | AATTCTTGCCAGAAC[C/T]GTTTTCATTCTGGGG | 83860 |
rs548927266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945512 | ATCTTCCCTTCTTCT[A/G]GTTAAGTGGATTCCC | 83860 |
rs548948612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7954624 | GTCCCAGTTAACACA[A/G]AGCTCTCCATAGTGA | 83860 |
rs548969641 | in-del | -/T/TTTTTTTTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838908 | TGGAGGCATTGCTTG[-/T/TTTTTTTTTT]TTTTTTTTTTTTTTT | 83860 |
rs548970663 | snp | A/G | 5.34726e-05 | 0.00517044 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818709 | GCGTCCACGCAGCGG[A/G]ATGTGCGAGAGTTAC | 83860 |
rs548989720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7851185 | AAGTTGCAATTAAAA[A/G]TATGCTAGTCAGGGG | 83860 |
rs549008622 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7857456 | GACGCCTACAGAGTA[G/T]CCATGGGTACCCCCA | 83860 |
rs549032299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819363 | TGACAGCTCTGCTCC[C/G]TTAGGGACACTGCCT | 83860 |
rs549047336 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867264 | ACTGTCACACACACA[A/C]ACACACAAAAAACAA | 83860 |
rs549089011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7844049 | ACTTTAGTCATTGAT[A/G]CCTTGTTTTAGAAAG | 83860 |
rs549112287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826011 | CATTTCTTAGAATCG[C/G]TTCTACTTTAATAGC | 83860 |
rs549112841 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887639 | CCTGGGACTAAAACA[C/G]ATAAGAGCCGCTGGG | 83860 |
rs549116384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014272 | AAAAACTGAAAAGCT[C/T]AACCAGAATTTATGC | 83860 |
rs549156607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7949490 | CTTTCCCTTTGCATC[A/G]CATTATGTAAGTCCT | 83860 |
rs549168362 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7823688 | TGCCCAGGCTAGAGT[A/G]TAGTGGCACGATCTC | 83860 |
rs549203322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7823834 | GAGACGGGGTTTCAC[C/T]GTGTTGACCAGGTTG | 83860 |
rs549209246 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7970171 | TAATTGGGAGTTGTC[A/G]ACAATGGAAAGCCCA | 83860 |
rs549239486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912898 | TGTTAGGTTTTTTGT[A/C]GGTGTCTGCTCGGGC | 83860 |
rs549247192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927644 | TAATGCCCAGAATCT[C/T]TTCAGACCCTACTTC | 83860 |
rs549255062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920406 | GAATGCTATGGGTGC[A/G]TTGTGTGATTTCAAT | 83860 |
rs549255114 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820410 | AATGAACTGATAAAC[C/G]ACTACCCTAAAAGCC | 83860 |
rs549258532 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817154 | GAAATCCAAGGCGCA[A/G]GAGAGTTTCAATGTT | 83860 |
rs549284685 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873623 | CCGAGTTCTCCCCCC[-/GT]CCCCCCGTCAAAAGG | 83860 |
rs549316512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992319 | AAAGTTGATCTGCAT[C/T]TAACACATACTGATT | 83860 |
rs549346249 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953189 | CTTCGGTTCCATTTT[C/T]CCAGTCTTCTCACTT | 83860 |
rs549375377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7872306 | AAAAGCAATGTTCTC[C/T]GTGTAATTAAAATCA | 83860 |
rs549379071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991461 | CACCATTGTTTTTTT[C/T]CCCAAACAAATTGTT | 83860 |
rs549379608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969463 | TGTTTTATTAAAATT[G/T]TGGTTTCTGTGTGGG | 83860 |
rs549424128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886499 | AGTTTGGTTTTTGCA[A/T]TTATAGACCTGGCTT | 83860 |
rs549428984 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7955359 | CATTTTTCATTTACA[C/G]ATTCTGACACAAGAT | 83860 |
rs549433560 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838509 | GCCTTAGCCTTCCAA[C/G]TAGCTGAAATTACAG | 83860 |
rs549433701 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7907956 | GAGCGGCAGCAGCAG[G/T]AATAGAAAGAAGAGG | 83860 |
rs549443292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7968816 | TTTCTATATTATGTT[A/G]AAATGGGATAAGTGA | 83860 |
rs549447520 | snp | A/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016144 | GCATATTTTAGCAAC[A/T]TTGGGATAAATACGG | 83860 |
rs549459786 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011705 | CCAAATGGGTTGATC[A/T]GGAAAGATTTTGTAC | 83860 |
rs549461198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8007206 | ATACAATATAGTAAT[C/T]AGAATAAATAATATA | 83860 |
rs549485322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879450 | AATGAAATAATGACA[C/T]CCACCCTCATCTTTG | 83860 |
rs549493074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935720 | TTACGGGAATCAGGG[A/G]GAGGCCCTACAGGTC | 83860 |
rs549495409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886983 | GCTTACACCTGTAAT[C/G]CCAGCACTTTGGGAG | 83860 |
rs549541726 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887091 | ATAAAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 83860 |
rs549544605 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947165 | CCCATCTCCTTCTCC[G/T]GCCCCTCTTCTGCTG | 83860 |
rs549553838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837937 | TTTGCATGGCTTTCA[A/G]TTGCTAAAATAATGT | 83860 |
rs549564807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937733 | ATAGTAATAGTCACA[A/G]CACCTAACATTTCAA | 83860 |
rs549573091 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7864137 | CTTGGTGTTGTACAT[-/TC]TCTGTGTTTTGACAA | 83860 |
rs549588263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999870 | ACTCAACTTAGACGC[A/C]CTCGATTGTGCAGCT | 83860 |
rs549605998 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970628 | AAAATGTTAGTTCCT[A/G]GAGATACCTTAGAGA | 83860 |
rs549607342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7956142 | TAGGGTATTCATGAA[C/T]TCTTTGTAGTATTCT | 83860 |
rs549611924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858481 | GCATCTATACTTAAC[C/T]GTTTTTTCACTAGTT | 83860 |
rs549621561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8001022 | TGTTTGTTCATCATC[C/T]ATGTAACCGATCTCC | 83860 |
rs549624868 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7954640 | AGCTCTCCATAGTGA[A/G]ATTCAGAGTGCACTC | 83860 |
rs549633953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832653 | GGTTCAAGTTTAAGT[G/T]ATTCTTGTGCCCCAC | 83860 |
rs549638416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8007893 | GGTCTAGTCTCTGGC[A/G]GCTGTAGAATTTGAA | 83860 |
rs549649474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8006264 | GCCTGTAATCCCAGC[C/T]ACTTGGGAGGCTAAG | 83860 |
rs549650048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870890 | TCTTGAAGCTCAGAG[A/T]TTCTTGTAATATGAA | 83860 |
rs549672669 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991206 | ACACACACATATACA[C/T]ACATACACATCCGTA | 83860 |
rs549673323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858856 | TGTCACTGAATGTAC[A/G]TGTGAGTGTGCGTGT | 83860 |
rs549684235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7968930 | CAAGCTTTTAGTTCC[C/T]CTTCGTGGGCAGTCA | 83860 |
rs549695498 | snp | G/T | 7.95767e-05 | 0.0063073 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014790 | GCGGGGTCAGCCCGG[G/T]CTTCTTCCCTGGCGC | 83860 |
rs549711666 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859416 | GGGGATTTCTGAAAT[C/T]ATCTGACATGGGCCT | 83860 |
rs549712878 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7928384 | GCACCTTTAGGTAAC[A/T]GAGTGGGCCACATAA | 83860 |
rs549715205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962978 | GTAACATCGGCTCCT[C/T]TTTGAAAGATTAGGA | 83860 |
rs549744246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7949031 | CCGGCTGCTGCCGCC[A/G]CTGCTGACAGCCGCT | 83860 |
rs549746680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893522 | AAACATTCATATCCT[C/T]AGGTATTTTTCTCTC | 83860 |
rs549747873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7976515 | CGCCTCCCGGGTTCA[C/T]ACCATTTTCCTGCCT | 83860 |
rs549759656 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7828702 | CAATGGGGGTCTTCT[-/G]GGGGGGGTCTGTTGA | 83860 |
rs549762581 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997950 | ACAAGTGATGAAAAA[G/T]TATATCATGTTATAC | 83860 |
rs549764310 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TAF3 | GRCh38.p7 | 10:8000337 | GGCCAGGCTGGTCTC[A/G]AACTCCCAACCTCAG | 83860 |
rs549796048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941638 | TGCTGCGCCGATGCC[G/T]TCGAGGCTGTGAAAT | 83860 |
rs549797806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955012 | TAGGTGAATGAATGA[A/G]TTAGTCCCAGTTAAC | 83860 |
rs549857731 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7860668 | AAGGTACCAATTAAA[-/T]TTTTTATATCATTCT | 83860 |
rs549879708 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930147 | AAGACTGCAGTGAAC[C/T]GTGATTGTGGTACTG | 83860 |
rs549879997 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892222 | TCTATTTCATAAGGA[C/G]TTGGCTAGGAAATAG | 83860 |
rs549889308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865717 | AAGGAAAAATAGAAA[A/G]TTGCTTAGTAAATGT | 83860 |
rs549902378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7838640 | ACCCACCTAGGCCTC[C/T]CAAAGTGTTGGGATT | 83860 |
rs549907569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008013 | TACCACAGCTCTAGC[A/G]ACCTGCGGCAGCATC | 83860 |
rs549915740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819926 | CCATAGCACAGATCT[C/G]ATCCTGTCATTATTC | 83860 |
rs549919569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901429 | TTCTACTCTTTCTGG[A/C]AAACATTCAATTAAC | 83860 |
rs550010417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906489 | AAACCTCTCTTCTTT[C/T]GGAGGAGAAAAGCCA | 83860 |
rs550022679 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8001077 | TTATTCTAGTTTTTA[-/T]TTTTTTTATTTTATT | 83860 |
rs550046204 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827233 | TGAGTTTCTGGTCTT[A/C]CCAAGTCACTTTACC | 83860 |
rs550065072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920548 | CCTATAATGAAATAG[A/G]AAATAATCTTCTGGT | 83860 |
rs550066833 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868397 | GTGGTGTGACATTAG[C/T]GGTCAAGTCTAGTGA | 83860 |
rs550067401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935752 | ACTGGGGAAGCACAT[A/T]CCAAAGAGAGGAAGC | 83860 |
rs550073442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907041 | GTGACTGTCATTGGG[G/T]GGACAGTGTTCGTAG | 83860 |
rs550087551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871881 | TGATTAACTATCCAA[A/G]TATTTCTAATATTTG | 83860 |
rs550097223 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7898739 | TTCAGACAATTAATG[-/T]TTTTTTCCTTTCACT | 83860 |
rs550098836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008639 | TGTGTCTTTCTTGCC[C/T]ATCTCCAGTGTGGAG | 83860 |
rs550102606 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939031 | GGAAGCTAAAACATA[A/C]CAGCCTGCAGAGAAG | 83860 |
rs550130171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942209 | GTCTAGCAATCACCC[A/G]TGACGATGCATAAAT | 83860 |
rs550181393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7859922 | TGCCTCTCAATCCAT[C/T]TCATCCTAAATATGG | 83860 |
rs550221881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902070 | GTGTGTGTTTTCTTA[C/G]AACCAGGACATTTCT | 83860 |
rs550223000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949665 | ATCAGTTGTAAGACA[C/T]ACCATTCATTTATGT | 83860 |
rs550238526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963046 | GTTGCTCTCTAGTGC[C/T]GTAACTCTAGCCGAA | 83860 |
rs550242854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860625 | TACATTGTTTTCAAC[G/T]TAACAGAATGACTCA | 83860 |
rs550245818 | in-del | -/CT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913023 | CAGGTTTGGTTTCCC[-/CT]GAGACCTCTTTCCTC | 83860 |
rs550296160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841102 | GTGATCCGCCCACCT[C/T]GGCCTACCAAAGTGC | 83860 |
rs550307502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7853666 | AAACTGCCTGGCCTG[C/T]AGCCTGATTCTGTAA | 83860 |
rs550334034 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7986801 | CTTCAGCTAAGAAAC[-/AG]GGGAAAAAAGGATAT | 83860 |
rs550341180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943634 | CCTCTGAGCTCAAGG[C/T]ATACAGATGGTAGGT | 83860 |
rs550350422 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7986398 | TTCTTCTTCTTTTTC[C/G]TATATGTTGGTGATG | 83860 |
rs550370138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865239 | CTGGGAGGCCGAGGC[A/G]GGCGGATCATGAGGT | 83860 |
rs550371867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7921829 | TTTAAGAAACTACTT[A/G]TTTTAAAATGATTTT | 83860 |
rs550404502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950148 | TTGGGGAAACAGACA[A/G]GAAATGCATGAACAG | 83860 |
rs550406480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7973261 | AACACACAACTCAAT[A/G]ATAGTAGAGCAGAAT | 83860 |
rs550425098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8001826 | TTGAGCTAATTCTCA[A/G]TTGCACATGCGTAAT | 83860 |
rs550442821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7932626 | ACCCCATTCTTAGTC[C/T]AAAATACAAGTGTGT | 83860 |
rs550446322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917506 | CAGGGGCCAGTTCCT[A/G]TGGGGCCTTATAGGC | 83860 |
rs550468705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865446 | ATCGCGCCTCTGCAC[C/T]CCAGCCTGGGGGACA | 83860 |
rs550486279 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860804 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGA | 83860 |
rs550490014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946848 | TAACAACTTTTTTTG[C/T]ATATTTGATGCTTTT | 83860 |
rs550509848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910896 | GCTTTCTTAAGTTGT[C/G]AAATAAGAACAAAAT | 83860 |
rs550521992 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855867 | GCGGGAGGATAGCTT[A/G]AGCCCAGGAGTTTGA | 83860 |
rs550523279 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7836255 | TCAGACCCTGCAACC[A/T]GTTGCAGTTGGCCAT | 83860 |
rs550548307 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7910537 | AGGTGCCCGCCATCA[C/G]GCCTGGCTAATATTT | 83860 |
rs550560466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904352 | TTTGTAGCCCTAATA[C/T]AACTGAAATGAAATG | 83860 |
rs550563357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934508 | GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCATTGC | 83860 |
rs550572185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960054 | TAGAAGAGCAGGATG[C/T]ACCATAACATACTCT | 83860 |
rs550574509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7966517 | CAGCTTTGCTTTTCA[A/G]TCTGTGGTTTCTTGG | 83860 |
rs550578450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862692 | TTCCCTCCTCCCCAG[C/G]GGGATCCCCAGGCAA | 83860 |
rs550583391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831043 | CAGTGCTGATGCTCA[G/T]TGCCTAGATCCATTA | 83860 |
rs550586095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8004901 | TCTAGAATTATGATC[A/G]AACATGCACTAATTA | 83860 |
rs550644183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863120 | CCAGGAAACTGTGGT[A/G]GACTAACTTCTTGGA | 83860 |
rs550647538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011443 | CTGTTTTTGTTTGTT[C/T]GTTTTTGGTTTTTGT | 83860 |
rs550665579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975113 | AGATGAAAATAATTC[A/G]TGGAACAGAAAGACT | 83860 |
rs550680821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863828 | ATGTTTTATAGTTTT[C/T]AGTGCATCTCTTATA | 83860 |
rs550688562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7940092 | ATACAAAGGACTGCA[A/G]TTCATAATGGAGTCA | 83860 |
rs550698627 | in-del | -/A | 0.0741063 | 0.177655 | intron-variant | TAF3 | GRCh38.p7 | 10:7999427 | TGTCTAAAGGCTGTT[-/A]AAAAAAAAAAAGAAA | 83860 |
rs550707004 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7856697 | AAAAATGGCTTTTTC[C/G]AAATCTAGGGCAGAA | 83860 |
rs550712023 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906589 | TTTGCTTTATGGACC[C/T]GAACAAATGTGACAC | 83860 |
rs550722048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918990 | CCAGTTGAGGGGGCT[G/T]TGATGGAGGTAGACT | 83860 |
rs550740782 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957060 | TCAATACATTCTCAC[A/G]CGTGGGAAAAGCAAA | 83860 |
rs550743342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875597 | TAGCATGAAAGAGAA[A/G]TTGACTGCCTCTTTT | 83860 |
rs550754169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835104 | GAGTTAGTTTTCTGA[G/T]CCTTTAGAACACAGG | 83860 |
rs550754176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841906 | AATCAGGTAGAGCTC[A/G]GGATTGTAAAACATG | 83860 |
rs550754414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998993 | CAAAGCCTTCAGGAT[C/T]TGATTGTACCTGGTG | 83860 |
rs550770197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828428 | CTTTATCTGATTATA[A/T]GTTTAGAAGTGAGAC | 83860 |
rs550785196 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946243 | ACCTACCCAACCCAC[C/T]TCCTTTCCTCTTGCC | 83860 |
rs550802212 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982372 | GGGCAAAAAAATACA[G/T]TTTTAAAATTAATTT | 83860 |
rs550802265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961249 | AGAGAATCTAGAATG[A/G]CCCCAGGTTCCTGAC | 83860 |
rs550802368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968176 | ATGTGAGCAGCTTTA[G/T]GTAAGGCACCAAAGG | 83860 |
rs550817035 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887285 | ATGATGAGGAAAACT[G/T]AATCTAAAGCAGTTT | 83860 |
rs550817262 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7998191 | CTTGTCAACACTGAG[A/T]AGCCACTTTAATGTT | 83860 |
rs550824454 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817210 | AGCTACAAAATAATC[A/C]AGTACGGCTAGGACT | 83860 |
rs550863479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967350 | TTCAACAGCCATTAT[G/T]AATTTGAGTGAAGCC | 83860 |
rs550911326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960570 | CAGGCACGGGGAATC[A/G]CATGTGCAGAGGTAC | 83860 |
rs550919713 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7895034 | GTGCCCACCACCATT[-/C]CTGGCTAATTTTTGT | 83860 |
rs550931531 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885425 | TTCTTATGTAAAATA[A/T]TAATATGGCTCCAAA | 83860 |
rs550955681 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914676 | TCTATTATAAATGTC[C/T]AGTTTCTTCGTATAC | 83860 |
rs550969639 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912744 | ACAAATCCAGATCCA[C/G]TTCAATGGTTCATTG | 83860 |
rs550969891 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898629 | CAGCCTCTCTCTCCC[A/C/G]CTCAGTTGTAAGATG | 83860 |
rs550982154 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919446 | AGGTCTGTGGTCCTC[C/T]CAAGCTTGATGTTTT | 83860 |
rs551005379 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822245 | CTGAAATCATGGTTA[-/A]AAAAAAAAAAAAAAG | 83860 |
rs551007539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878482 | GTAAGGGTACAGGTG[A/G]TGTTCTCTGTCTTGA | 83860 |
rs551026908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011575 | GCAACCACGCCTGGC[C/G]TATTATTAAATTTCC | 83860 |
rs551040307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919382 | CCTTGCTGAAATCTT[G/T]CAGGGTGTACTGTCC | 83860 |
rs551052845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981718 | TCAGTAACTTCATCA[C/T]CAGCCCTCGTCCTAA | 83860 |
rs551072821 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914320 | CTCATCCTTCAAGTA[C/T]TGGCTTATGTTAACC | 83860 |
rs551079469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7921760 | AGATTTCAGCCAAAT[C/G]GCTGATATTATTGTT | 83860 |
rs551091284 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7904789 | TTGGGGTTTTTTCCA[C/G]ATTCTCTGGAAAAAC | 83860 |
rs551099456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824637 | GCTTTCCATGCTATG[C/T]CAACTTTATAAATTC | 83860 |
rs551108622 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844010 | GTCAAAGAATGTTTT[-/A]AAAATCTTGAGAAAA | 83860 |
rs551143846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876959 | TCTAAATAAAACTGT[C/T]ATCCTGATTTTCAGA | 83860 |
rs551144359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912918 | TCTGCTCGGGCTGCC[A/G]TCACAAAATGCCACA | 83860 |
rs551156828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899188 | CGATCCTGGGCCTCA[C/T]CTACATCCTTGCCTG | 83860 |
rs551170000 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887820 | TTTAATTGGCCACTT[-/A]AAAAAAAAAACACCA | 83860 |
rs551179066 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891093 | GTGTTTTAGAGAAAA[A/G]TGGAGAGGACATTTG | 83860 |
rs551192444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850247 | ACTACTCTTTTCATT[A/G]ATTTGCTTTCATGAG | 83860 |
rs551198048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7966580 | TCTCATAAACTTTCC[A/G]AAAAAGTATCTCTTC | 83860 |
rs551199842 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7890985 | AATTTTGCTAAGCAT[G/T]TAGCTGAACTTGCGG | 83860 |
rs551207011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8008157 | GCTAGAGTGCAGTGG[C/T]GAGATCTCGGCTCAC | 83860 |
rs551231695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7927344 | TTTTCTGAACATCTT[C/T]CAACATGTTGGTGGT | 83860 |
rs551258186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975535 | GGCATCACTCGGTGC[C/T]CTAGGGGATGGTTTT | 83860 |
rs551263223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884394 | AGAGCTCTGCCTCCT[G/T]TTTTTTTTTGAGATG | 83860 |
rs551302564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990730 | CCCCATCAGTTCAAA[A/G]GTCTCTGTAGGGCCT | 83860 |
rs551303794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005565 | CTGGGCTTTGACATT[C/T]GTCCTCTTCATCATA | 83860 |
rs551306698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918176 | ACTAATGAAATGCGT[A/T]AAACAAGAAACAGTT | 83860 |
rs551308657 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865279 | AAGACCATCCTGGCT[A/T]ACACAGTGAAACCCT | 83860 |
rs551323747 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836417 | GTACCTGGGATTAGA[A/G]GCATGAGCTACCAAG | 83860 |
rs551325268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976393 | ATGGGACTACAGGCA[C/T]CCGCCACCATGACTG | 83860 |
rs551325279 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7863568 | CGAGCTGAGATCGCC[C/T]CACTGCACTCCAGCC | 83860 |
rs551329033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869225 | ATAATCCCATGAAGA[A/T]TAATCCTTCCTGACT | 83860 |
rs551343646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947555 | GACGGCTTCACTGAG[A/G]GGTGACATTAGAGAG | 83860 |
rs551362730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824721 | ACCAACAAACTTGCA[A/G]CTGACATTACCAAGC | 83860 |
rs551367711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999205 | ACTGCAGTAGTAGGT[A/G]TTCTATTTAAAGCTG | 83860 |
rs551367956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7911660 | TTCATTCATCCTGAA[C/T]GTACGCTTAGTTTGT | 83860 |
rs551381291 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858307 | ATGTTACAAGCAATT[A/G]CCAGTAATATTGTAT | 83860 |
rs551416906 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999386 | TCTTTGAAAAGGCAA[C/G]ACCCAAAACTACGTA | 83860 |
rs551418902 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889637 | CAGACTCATATTCAG[C/T]GGCTTACTGGGCAAA | 83860 |
rs551424695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857403 | TTAAACAGTCTGTCC[A/G]GGAGAAAGTTCTCTG | 83860 |
rs551426677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7849871 | TTTTTGTAGATACCA[A/G]GTTTTCACCATGTTG | 83860 |
rs551432116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7926925 | TACTGTTTGGTTCAA[C/T]GTGTGTATATATATT | 83860 |
rs551432124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935066 | TGGATCACTTGAGGT[C/T]AGGAGTTCAAGACCA | 83860 |
rs551445185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960648 | GGAATGGGTAGAGCA[C/T]GCAGGGGCTCACTGT | 83860 |
rs551461584 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003341 | CACTACCTTTACACT[A/G]CAGTTTATATAATAG | 83860 |
rs551491996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7934548 | TTTCCAAGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 83860 |
rs551493575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850315 | AGGACAATTCATGAT[A/G]TCAGTTTGGAGAAGC | 83860 |
rs551502644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913032 | TTTCCCCTGAGACCT[C/T]TTTCCTCGGCTTGCA | 83860 |
rs551504637 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884568 | ATTTTTGTATTTTTT[A/T]GTAGAGATGGGGTTT | 83860 |
rs551513327 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867088 | ACATGGCGAAACCCC[A/G]TCTGCACTAAAAATA | 83860 |
rs551532097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868457 | CAGCCAAGCTCTAGT[A/G]ACCATCAGGAGTGGA | 83860 |
rs551547180 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817983 | AAATATTATCGATCT[C/T]GATGACTGAGTTTTT | 83860 |
rs551547688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955140 | ATACCTAAATTCAGA[C/T]GAATAGAAAGGTATT | 83860 |
rs551553788 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935427 | CGTCTTGACTAAAAA[C/T]ACAAAAAATAGCCTG | 83860 |
rs551555043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982762 | AGTTTTTCAAGGCAG[G/T]AAATTTAAAAATTAA | 83860 |
rs551578255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822514 | TCAAAGACTGCAGAA[G/T]TATGTGGAGTTAGAA | 83860 |
rs551585704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858504 | CACTAGTTCCGGATC[G/T]TACTGATTAGGTACT | 83860 |
rs551626646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830316 | ATGTGCCCAACCCCA[C/T]CCCACCCCTTCCTCC | 83860 |
rs551635606 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7843021 | TGCACCTGCTAGGGC[A/G]TAGTCTGTGTCTGTC | 83860 |
rs551645437 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840292 | TGAATAGCTCTGACT[A/G]CAGGCGCCCGCCACC | 83860 |
rs551664110 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962201 | CTCAAGTCTTATACC[C/G]TAATCATTTATCAGA | 83860 |
rs551682540 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7884996 | TAATTTTTGTTCAGT[G/T]TTTTTTTTTTAATTT | 83860 |
rs551688278 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863439 | AGGATGGTGAAACCC[C/T]GTCTCTACTGAAAAT | 83860 |
rs551693473 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7856420 | GTAGGTGGAGGTTGC[-/A]AGTGAGCCGAGATCA | 83860 |
rs551696195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831805 | CTAGACTCAGCATGT[A/G]TAGTCATGTTCTATG | 83860 |
rs551696606 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7923123 | TATTTACATTCTACT[A/G]TGAGTATGACAGAAC | 83860 |
rs551698880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837414 | TTGAGAGGTTGAGGC[A/G]GGCTGATCACTTGAG | 83860 |
rs551700619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912331 | TCTCAAAATCCTGGG[C/T]TCAAGCGATCATTCT | 83860 |
rs551702335 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012262 | AAAATTTATGATTTA[G/T]ATGACATACAAAGGC | 83860 |
rs551722607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953955 | AACACAGAGCTCTCC[A/C]TAGTGAGATTCAGAG | 83860 |
rs551770793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920292 | AAAATTAAAAAATTT[A/C]AACATACGTGTGTGT | 83860 |
rs551778050 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7827770 | GGGTGACGGAGCGAG[A/G]CTCTGTCTCAAAAAA | 83860 |
rs551823347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929933 | AGGGCCAGGCGTGGT[A/G]GCTCACACCTATAAT | 83860 |
rs551830583 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966298 | CCGTTTTCTGCTTTA[A/C]TAAGATAAGGGCACA | 83860 |
rs551833025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975576 | TGGATGTATGGTGGA[A/G]TAACTAAGAGGTAAA | 83860 |
rs551841536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828258 | CTGAAAAAAAGAGAC[A/G]AATCAATGTAAAGTA | 83860 |
rs551845357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871600 | AGGCATGTGCCACCA[A/T]GCCTGGCTAATTTTT | 83860 |
rs551845378 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008717 | CAGCCCCTGTCAGGC[A/C/G]CCCCCGAGGACTCAG | 83860 |
rs551861992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7861261 | AGCCACCGCATCCGG[C/T]CCTGCACGGCTAATT | 83860 |
rs551881732 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881561 | TGAAGCTGGAACGTA[A/G]TAAGTTTTTTATATC | 83860 |
rs551883784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941589 | CCTCTGCTTCGCCAC[C/T]GCCTCACTGTATCCT | 83860 |
rs551884071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937157 | TATCTGTTTGCAGGT[A/T]TTTGTGGGGACATAA | 83860 |
rs551900113 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818598 | CGGGGGTCCGGGGGA[C/G]CCTTTCCCCGCCGCG | 83860 |
rs551900872 | snp | G/T | 0.00219539 | 0.0330586 | intron-variant | TAF3 | GRCh38.p7 | 10:7975137 | AAAGACTGAAGATAC[G/T]GTAAATAAGCAGATG | 83860 |
rs551937426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958744 | ATGCTTCATAACTTC[C/T]ACGCGCGTTACTTAT | 83860 |
rs551957194 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960198 | TTAATAAGTGAATGT[A/T]CATTCACTTTCAGAA | 83860 |
rs551967346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7843912 | TATAAATAAGAAAAC[A/G]GACTGTTTTATATGG | 83860 |
rs552000074 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7962307 | CTTACTGCCTCTCAC[A/G]TCACTTCAGTAATCC | 83860 |
rs552000769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957663 | GTTTCTCACATATGT[A/G]CAGAAGAGTCCTTTT | 83860 |
rs552016490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014143 | TTCCAGTAATGTTCT[A/G]TAGGAGCTGTAGCAC | 83860 |
rs552028656 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7837878 | TGTTTATTCTTACAA[A/C/T]GTAGATTACTTACTG | 83860 |
rs552032454 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7821510 | ACAAACTGATGGTGT[A/T]TGTTTCTTCTAAAAG | 83860 |
rs552049737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834030 | GTTTGGGTTCCTTAT[A/G]TATTTTGCCTTTTTT | 83860 |
rs552061520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968734 | CATCTAGTAAGTGAT[A/T]GAACAGGAGCCAAAA | 83860 |
rs552081486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7895839 | GCGCAGTTTTTCTGG[C/T]GTTCAGTAGGCATTC | 83860 |
rs552087052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006487 | ATATAGAAAGTGCTC[A/G]ATAAATATTCATCGG | 83860 |
rs552104449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988488 | GAGGCAGGAGAATCA[C/T]TTGAACCCAGGAGGT | 83860 |
rs552124616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7848152 | CTTAACAATATAAAG[C/G]TTCCATTGGAGCCAG | 83860 |
rs552125804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878547 | CCACACACTTAGGGT[A/G]TATTAACTTTGTATG | 83860 |
rs552133437 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7874786 | TTTCTTTTCTAGGTG[C/G]AGATTACATGGAAAA | 83860 |
rs552169769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988095 | TTATGTTTGTAAGTA[A/G]TGTTTATAAGTAACC | 83860 |
rs552172182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915728 | CACGCTTGTAATCCC[A/G]GCACCTTTGGGAGGT | 83860 |
rs552182858 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7954866 | AGTGCACTCCATAGG[C/T]GAATGAGTGAATTAG | 83860 |
rs552206404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952235 | AGATATTGACATTGT[C/G]TGAAGAGATCTACTT | 83860 |
rs552210826 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7883479 | TTCCAGATTTCTCCA[C/T]TGTCAAGTTATTACT | 83860 |
rs552220604 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948884 | GCTTTCTTTATTAAA[C/T]GGTTTTGTTAAAATC | 83860 |
rs552241572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822905 | TATCTAACTTTTTAT[C/T]TCTGTTTTATGTGGT | 83860 |
rs552246312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875471 | TGATTGTGTTATAAG[A/G]AAGAGAAAACCAAGA | 83860 |
rs552256826 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7864812 | TCAGTTTTAAGGAAA[A/T]ATAGTTTATCTTTTT | 83860 |
rs552274189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884106 | CTTGTCAACTGCCCC[A/G]CCTCTCAATACTGCC | 83860 |
rs552275812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876199 | CCAAATAGTGATGAA[A/G]TCGACTATTTTAGTA | 83860 |
rs552283713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890133 | CACTCTCAGTCACTT[C/T]GCTGGGACTTTTCTC | 83860 |
rs552290582 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7987106 | GCAGGCAGATCACTT[C/G]AGCCCAGGAGTTCAA | 83860 |
rs552344674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7906707 | CGAATTAAATAGAGC[A/G]CAAGCAGCATGTAAG | 83860 |
rs552350267 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854889 | TGAACAGAATGAGAC[A/G]GCAAAAGTGGTATTT | 83860 |
rs552365497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004119 | GCAGTGGCATGATCA[C/T]GGCCCACTGCAACCT | 83860 |
rs552370656 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7885927 | TTCCTCTGTTGATAC[-/T]TTTTTTTTAATTACG | 83860 |
rs552388127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835600 | TCTGAGAGCTCCTGG[A/G]CTCAACTTCTAGCCC | 83860 |
rs552395070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7887936 | GCAATATCAGAATAA[A/G]TCGAGGAACTTTTTT | 83860 |
rs552440890 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7915224 | GGATTACGGGCAGGG[-/C]ATGAGCCACTGCGCC | 83860 |
rs552443039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981030 | GATGGAACTGTCAAG[A/G]AAGACTTGGCAGAAT | 83860 |
rs552444502 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869454 | GTCTTTCCATGTCTG[G/T]TAACTTATCCTCATG | 83860 |
rs552454976 | snp | A/C | 1.73685e-05 | 0.00294685 | missense | TAF3 | GRCh38.p7 | 10:7964505 | CGACTCACATTCCCC[A/C]AACACCTGTGAGACC | 83860 |
rs552469833 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928860 | CTGACCTCTGGAGAA[A/G]TAGGCATATTATAAA | 83860 |
rs552518703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881669 | AACAATCATGCATTT[A/G]GATGTAATGAAAAAA | 83860 |
rs552563508 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905644 | CCCAGCACTGTGGAA[A/G]GCTGAGGCGGGCAGA | 83860 |
rs552598602 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7945535 | GGATTCCCTTTGGCC[G/T]CAGACACTCTCTAGA | 83860 |
rs552609702 | in-del | -/TG | 0.35445 | 0.227135 | intron-variant | TAF3 | GRCh38.p7 | 10:7838364 | GCCAGTTTTGTTTTT[-/TG]TTTTGTTGTTGTTGT | 83860 |
rs552623963 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939476 | GTGTCCAGCGACTCA[C/T]GCTTAAACACCCAGT | 83860 |
rs552669983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861308 | AGATGGGGTTTCACT[A/G]TCTTGGCCAGGCTGG | 83860 |
rs552676094 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877690 | TCTGAGATTACAACC[C/G]TACTATTTAAAAAAT | 83860 |
rs552696518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7929033 | GCAAAATTAGCAGAA[A/G]CTTGAATTTAATGTA | 83860 |
rs552703993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7826386 | TAGCAAGGAAATGTA[A/G]CTAAGATAACAGGTT | 83860 |
rs552711624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966229 | TGCGCCATTTTGGCA[C/T]GTGTTTAGGATTATG | 83860 |
rs552733231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854842 | AACATTTAGATTGTA[G/T]TGTGAACTTCTGAAC | 83860 |
rs552809565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7925487 | TGATTATTTATAACA[A/G]ACTTACATGGTGGTC | 83860 |
rs552809610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7933887 | TGCACGTTTTCCCCC[C/T]GATTTTAGCATTTCT | 83860 |
rs552811374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903612 | TCATCTTTGGAATTG[C/T]TTAGCTGATGCAGTT | 83860 |
rs552826558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820250 | ATTCTGTGCATATTT[A/C]TTTTATATTATTTGT | 83860 |
rs552843629 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858924 | TGCTGGCCTCTTCAG[C/T]GTCTTCTGGGCTCTA | 83860 |
rs552858901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7951276 | CTTAAAACAGCAACC[A/G]TTTACTAGCTTACAA | 83860 |
rs552863035 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7887802 | ATTAAAATCCTTTAT[A/C]ATTTTAATTGGCCAC | 83860 |
rs552871064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7889403 | TTAATCTTCACAACA[A/G]CCCTGTAAGGCAAAT | 83860 |
rs552936386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873909 | GTATTGAGCACTTAG[G/T]TTCCCTGTATCATCT | 83860 |
rs552973655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957196 | TAATACCTATCCAGA[A/G]CTACCTTTCCTTAGT | 83860 |
rs552978281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972856 | ACTAGTTAGCCTCCC[A/G]TGGAGAACAAAATTT | 83860 |
rs553007539 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903947 | TGTGAGAATATTTTA[C/T]GGTATTGTAGGTATC | 83860 |
rs553010873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868509 | AGTTCTAGTGACCAT[C/T]AGGAGTGGAGGCAGT | 83860 |
rs553022126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903083 | AAAAGTTATCCTGGC[A/G]TGGTGACACACCCGT | 83860 |
rs553036847 | snp | A/G | 3.81352e-05 | 0.00436648 | splice-acceptor-variant, intron-variant | TAF3 | GRCh38.p7 | 10:7963918 | TTTTCTTCCTTTACC[A/G]GAAGAAGAAGAAGAG | 83860 |
rs553048241 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7828805 | TTGGGAGGCCGAGGT[C/G]GGCGGATCACTTGAG | 83860 |
rs553073887 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7892054 | AATTTAATTTCAAAA[-/C]CCAGATGTTTAATTA | 83860 |
rs553115041 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7847638 | TCTGTAGAGACAGAG[A/T]CTTGCTGTGTTGCCC | 83860 |
rs553117160 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7840911 | CTGGCGTGCAATGGC[A/G]TGATCTCGGCTCACT | 83860 |
rs553118742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937987 | TGAGGGCCGCTTAGA[A/G]GGGATTTTGCAATAG | 83860 |
rs553153358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987373 | CTGTTCAGCAGCTTA[C/T]CCCCTCCCCTCTAAC | 83860 |
rs553159449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915272 | TTTATGAAGAACCTG[C/T]GCTCTTCCCTTTGCT | 83860 |
rs553179131 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7911100 | TGAGGGAGAAGACTC[A/G]CACCTGAAAGTGTAG | 83860 |
rs553214720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995705 | GATAAAATGTTTGCT[A/C]CTTGATATGTACTTG | 83860 |
rs553215779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862801 | TGTTTTTTGGTCTGG[A/C]CTTTTTTCACCAATA | 83860 |
rs553215783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938522 | TGAAAACTCATGTCT[A/C]TAGTTGACTGAGAGA | 83860 |
rs553218166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882014 | CAGTTAAACAGGTGT[C/T]GATTGGGCACCTACA | 83860 |
rs553265446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866243 | TCTTCCAGGCACGGG[A/G]GATGGAGCAGTCAAT | 83860 |
rs553276154 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896228 | TAATAAAATAATAAC[C/G]CTTCTCTATATTCTT | 83860 |
rs553288165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7849914 | TTGAAATCCTGAGCT[C/T]GGGCAGTCTACTCAC | 83860 |
rs553291351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889423 | GTAAGGCAAATACTA[C/T]TCACATCTGTCTGTT | 83860 |
rs553303337 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851574 | CAACAATTAACTTCC[A/G]TCATCACCCAGCTTC | 83860 |
rs553303652 | in-del | -/GAA | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7900270 | AAAAAGTCAAGAAAT[-/GAA]GAAGAATACAAATAG | 83860 |
rs553309271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976605 | ATTTTTAGTTTCACC[A/G]TGTTGGCCAAACTGA | 83860 |
rs553347600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829645 | GACATCATATCAAAG[G/T]TCTATCCTGTCATCA | 83860 |
rs553348900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002696 | TTTTAAATGTCCATA[A/G]AGTCAATTTCATTAT | 83860 |
rs553352460 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975988 | AAAAATACCAATCCT[A/G]CAGCCCCACCGAAAG | 83860 |
rs553355388 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7883036 | TGGCTTCTCATATGT[A/T]ACAGAACAGTTATCA | 83860 |
rs553359851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910524 | TAGCTGGGACTACAG[G/T]TGCCCGCCATCACGC | 83860 |
rs553366785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7917033 | TTACTAAGTTTATTC[A/G]TTCAGCGAATATTCA | 83860 |
rs553370578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7976159 | GAACAGGTCAGATCT[C/T]TCTGAGGTCTTTATC | 83860 |
rs553447062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968482 | ACCTGGAATAAGATC[C/G]AGGACAAGTTTTTTA | 83860 |
rs553463424 | in-del | -/CACACACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006215 | ACACACACACACACA[-/CACACACACA]AATTAGCTGGGCGTG | 83860 |
rs553493103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846066 | TGGGTTCACGCCAGT[C/G]TCCTGCCTCAGCCTC | 83860 |
rs553497024 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7979913 | ACCTGAAAGTTAAGA[A/C]TGTGTTTTATATTTC | 83860 |
rs553517431 | snp | A/G | 0.00122924 | 0.024761 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964791 | CCCTAAGAGAATTTC[A/G]GGCCCGGAGTGTACT | 83860 |
rs553533616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7882144 | GGGAAAACAATTATA[A/G]ATTTCAAGATGTTTT | 83860 |
rs553537251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864615 | ATTTTTCTTGGGTAA[A/G]TGTCCAGGAGTAGAA | 83860 |
rs553542058 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923160 | ATAGCAAAACCATGC[A/G]TGTTGGAGGCTAACA | 83860 |
rs553560219 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7834817 | AAACAGGTAAAAAAA[A/T]TTTTTTTTGCTCATT | 83860 |
rs553563822 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818309 | ACTGGCGTTTTCGTC[A/C]CCGCTGTCCCCCAGG | 83860 |
rs553608700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934769 | TTAATATTTAAAAGT[A/G]CTATGATATAGAGCA | 83860 |
rs553636173 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881386 | ATATGCCTTTAATGC[C/T]GCCTCCAAGTCAGCA | 83860 |
rs553671873 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7936035 | GCTGTGGGGATAATC[-/T]TAAGAGACACGGCGG | 83860 |
rs553680226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832112 | TTTTCTTTTTCACCA[A/T]GCTGTGCAATGTATC | 83860 |
rs553687631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878970 | TGACCTCAAGCAATC[C/G]GCTCACCTCAGCTTC | 83860 |
rs553705029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924877 | TCATATCTCACTTAA[A/G]ACGTAAGTTGTTTAG | 83860 |
rs553714049 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7837620 | TGTACTCCAGCCTGG[A/G]CAAAAGAGCAAGACT | 83860 |
rs553738098 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7925573 | CTTCGGGAGGCCAGG[A/G]CAGGTGGATCACTTG | 83860 |
rs553740181 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7828912 | GGTGGTGCCTGTAGT[C/T]CCAGCTACTCGGGAG | 83860 |
rs553799400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7927925 | CCTTGGAATTACAGG[A/G]TCAAGATTTTCTTCT | 83860 |
rs553817654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825057 | TTTGATCATATAGAA[C/G]TTTTGATTATAAAAT | 83860 |
rs553818230 | snp | C/G | 6.62998e-05 | 0.00575721 | intron-variant | TAF3 | GRCh38.p7 | 10:8013863 | AGGGCGCCCTGCCGG[C/G]CACACTCATTAGGCA | 83860 |
rs553823125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914031 | ATGTGACATCAACCA[A/G]TTGCAATGTGGTCCT | 83860 |
rs553845788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865151 | CAGGAGCTTCAGGAG[A/T]GGAGAGGGCAGGGAA | 83860 |
rs553851385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922420 | TTTCTCCAAGCCTCT[C/T]TTTTCTGTAAAACAT | 83860 |
rs553852419 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998775 | ACCCAGGAGGTGGAG[A/G]TTGCAGTGAGCCGGG | 83860 |
rs553891871 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000635 | ATACAAAAAATTAGC[A/C/G]AGGCATGGTGGCACG | 83860 |
rs553893799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008032 | TGCGGCAGCATCACC[A/G]GGACAGAAGCTGCCG | 83860 |
rs553925543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942557 | ACAAAATCCGCTGGG[G/T]TTTCCTGGAGAAAAC | 83860 |
rs553931880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992989 | CTCATATAATCACAA[C/T]GTTATTATCATACAT | 83860 |
rs553937866 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924801 | ATTTTAAACTTAAAG[A/G]AAAACCCCTAGTTCT | 83860 |
rs553948553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818957 | GTCCCTCCGCGTCCC[C/T]GGGGTGTGCATCCCG | 83860 |
rs553959989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7992952 | ATTCTTCAGTATGCA[A/G]CTCTAAAAATATGGT | 83860 |
rs553968380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839987 | TCTGCCTTTCAAAAA[A/G]GTTTTTCCTTTAATT | 83860 |
rs553976983 | in-del | -/A | 0.465158 | 0.127307 | intron-variant | TAF3 | GRCh38.p7 | 10:7822488 | AACCCATACTTATAG[-/A]AAAAAAAAAATCAAA | 83860 |
rs553979308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955813 | TCATTATTCCTCAGG[A/G]GAATGTAGGGAGTGT | 83860 |
rs554006970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886042 | CAAGTGATCCTCCTG[C/T]GTCAGCCTCCCAAGT | 83860 |
rs554006975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014390 | ACAAAGCCGTGGCTC[A/G]GAAGACTTCTATTCC | 83860 |
rs554022775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901499 | AACCATTGAAAACTA[C/G]TTTCCTTTGAAATTG | 83860 |
rs554022961 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7838059 | CTAAAGGCAGATGCT[C/G]CTATCATTCCCATTT | 83860 |
rs554081831 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7854352 | AAGATAACTGGAAGG[-/A]AATTATTTGCCCCAA | 83860 |
rs554083889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894657 | CTTACTATAAATGCC[A/C]AAATCATCTATGAAA | 83860 |
rs554089662 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866271 | AATAAATAGGCAGGC[C/T]CTGCTTCCATGGTGC | 83860 |
rs554092747 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TAF3 | GRCh38.p7 | 10:7986035 | GTGATCCACCCACCT[C/T]GGCCTCCCAGAGTGC | 83860 |
rs554108433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969989 | AAAACAGTAGTTTCA[C/T]ACCTTCTCGAAGAAT | 83860 |
rs554111856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860282 | CCCTGTCTGGAAAAA[A/G]AAAAGAAGAAAAAAA | 83860 |
rs554137715 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927591 | AGTTGCCTAACAACT[A/C]ATCTACAAAAATGAT | 83860 |
rs554139205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865205 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 83860 |
rs554139687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887306 | AAAGCAGTTTATGAA[C/T]TGATGCTGTAGTTGA | 83860 |
rs554156018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7993914 | TTTTTTACTTGCCAG[A/T]CTTCAGTGAAAAGAG | 83860 |
rs554172816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845849 | TTTTTGTTTTTAATT[A/T]TTATTTCTATTTGTT | 83860 |
rs554201026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880548 | TGGAATTTTCTTAGA[A/C]TACCCCACTCTCTGC | 83860 |
rs554202478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865586 | CCTCCCTGGAGGTGG[G/T]CGTAGTAACAGGCCT | 83860 |
rs554230227 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010096 | ATTTTTGGTGGAGAC[A/T]GGGTTTCACTATGTT | 83860 |
rs554259063 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7872732 | AGCAAATTCTTTATA[G/T]AATTTCTTTTTCACG | 83860 |
rs554264022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860397 | TGAGAGAATAAAGTT[A/G]TACCTTTGCCCCATC | 83860 |
rs554267538 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7929255 | GTAGTTTATTTTTTT[G/T]GTTGTTTTTTTTTTG | 83860 |
rs554279209 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938561 | GGCCAGTCAGACAAA[A/G]AAAAGAAAACGTGAG | 83860 |
rs554312852 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7838104 | GGAAGTTTAAAAATC[A/T]TAATTGAATTAACCT | 83860 |
rs554315643 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7956225 | CCGGGCGCGGTGTCT[C/T]ACGCCTGTAATCCCA | 83860 |
rs554317949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7949219 | TGGTTCTGTAAATCA[A/G]AGTCCACTTGCCCTT | 83860 |
rs554319266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7859400 | GTTTCAGGAGGGCAG[C/T]GGGGATTTCTGAAAT | 83860 |
rs554328973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842236 | TGAAGTGCTGTGGCA[C/T]GATCGTAGTTCACTC | 83860 |
rs554341284 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874565 | AGCTCTATAAGCTCT[A/G]TATATTTAAAGCCAA | 83860 |
rs554343334 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902515 | TTGTTTTCTCATGAC[A/G]AAACTCAGGGGAAAA | 83860 |
rs554345450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8001338 | TAGATTGTCATGTTT[A/G]TATCTTTGATTACTA | 83860 |
rs554358627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827992 | GCGAATATTAGTTCT[C/T]GTCCCCTTTTTCTTT | 83860 |
rs554376263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7838799 | TCTGGCTGCCTCTCT[A/C]TTGGCCCTCTCAGAT | 83860 |
rs554438318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970229 | TTTTATCCTGTTGAT[C/T]GAGGAATTGTTTTAT | 83860 |
rs554445485 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7963225 | TAATAATAATCCATA[C/G]TAAGTCCTATAATAA | 83860 |
rs554487130 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7893290 | GTTATTTAATAATCA[G/T]TTACTAATGATGAAT | 83860 |
rs554498497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832377 | TGACAAAATTTCCTT[C/T]TTTTTTTAAAGGCTG | 83860 |
rs554504862 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838584 | GTGGGATTTCACCAT[A/G]TTGGCCAGGCTGGTC | 83860 |
rs554505628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825722 | ATATGTACATTCCAC[A/G]TTTGTTTATCCATTC | 83860 |
rs554506033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853286 | GTTGGGTGAAAATAC[C/T]ATATAACTGTGCCTC | 83860 |
rs554539358 | in-del | -/T | 0.0108235 | 0.072764 | intron-variant | TAF3 | GRCh38.p7 | 10:8011246 | CAATATTACATTTCT[-/T]TTTTTTTATGTTTTC | 83860 |
rs554547660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888602 | TGTGTAACAGTTTAT[C/T]CATGCCCAGTTAGGT | 83860 |
rs554567204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922238 | TAAGCAAACTATCAC[C/T]GCACTAATGTTAATT | 83860 |
rs554568037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955907 | ATCAACATTTGTAAA[C/G]CTTTTGAAAGATAGG | 83860 |
rs554596628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880273 | CTCAAGTAACTTACT[C/G]CTTAGACTTTTTGGG | 83860 |
rs554599700 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015657 | AGAGAAAAAGCCATC[A/G]TTCAAAGAAATTTCC | 83860 |
rs554634455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908132 | CCCTGCCTTCTCCAT[C/T]GCCATTTCCTCTTGT | 83860 |
rs554638491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976734 | ACAGCATTTCAGATT[A/G]TTTTACCCCTAGCCA | 83860 |
rs554645544 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975046 | CACTGCACTCCAGCC[C/T]GGCAACAGAACAAGA | 83860 |
rs554686436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819594 | GAGTTTTAAATGAAT[A/G]TCTGGTAATATCTAT | 83860 |
rs554690844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870497 | CTTTCTGGTGGTTCA[C/T]TATAAAATACATTTT | 83860 |
rs554691138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8002002 | TCTAAGGCCCCATCC[A/G]TCGATCCTGTGAATG | 83860 |
rs554718848 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999208 | GCAGTAGTAGGTATT[C/G]TATTTAAAGCTGATT | 83860 |
rs554729564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860834 | AAATAGAGTCTCGCT[C/G]TGTCACCCAGGCTGG | 83860 |
rs554750981 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903948 | GTGAGAATATTTTAC[A/G]GTATTGTAGGTATCT | 83860 |
rs554752183 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7894875 | CTAATTCCCTTTTTT[G/T]TTGTTGTTGTTGTGG | 83860 |
rs554793758 | in-del | -/GGGGTGCAAA | 0.0154538 | 0.0865337 | intron-variant | TAF3 | GRCh38.p7 | 10:7831939 | TTTGTATATATCTGG[-/GGGGTGCAAA]GGGGTGCAAAGCGAT | 83860 |
rs554797286 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016702 | ATCTGAAGTTGCCAC[A/G]TTTAAGTGAGCAGGT | 83860 |
rs554809174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886775 | AGAGAGATGCACTTT[C/T]GTATTTCTGTACTTG | 83860 |
rs554814230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879755 | GTGGCTTTTAAAATA[C/T]TGTTTTGATTTTGGC | 83860 |
rs554816712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908756 | TTTACAGGGAAACCT[G/T]ATATGTAAGACAGAT | 83860 |
rs554818677 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824068 | GAAATTTGTTCTATA[A/G]TAGCTAATCATGAAT | 83860 |
rs554821648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895521 | GCACGAACACCTTGG[C/T]CTGCCACATCTATGC | 83860 |
rs554822361 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923822 | TTGAATTTTTGCACA[A/T]AATTGACTTTTTAAT | 83860 |
rs554844790 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7832848 | AGCCACTGCACCTGG[A/C]CCAGCATTTATCATT | 83860 |
rs554857420 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986678 | TCTTCAAGCTTGGCT[C/G]TCTCCTCCTTGTCTA | 83860 |
rs554877388 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015149 | GTAATTTAAGGATGA[C/T]AGAGTCTGTATACAG | 83860 |
rs554877475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7872037 | TTAAATATTGATTTA[A/G]GTTTAAAGTGACACA | 83860 |
rs554880071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902271 | TCTACTAAAAATACA[A/C]AATTAGCCAGGCCTG | 83860 |
rs554880089 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846168 | TTCACCGTGTTAGCC[A/G]GGACGGTCTCGATCT | 83860 |
rs554885174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888083 | AACTCTCATCCCCAG[C/G]TCTTTCTCTCCACTG | 83860 |
rs554953503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979357 | TCAAAAAATGAAAAA[A/T]AAATGAAAAAAAAAA | 83860 |
rs554955338 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7899012 | GTCAGTTCCCATAGG[-/T]TTTTTTCTTTTATTC | 83860 |
rs554971111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840103 | TTTTTTTTTTAAGTT[C/T]TAATGTTTCTAAATT | 83860 |
rs554972030 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870826 | TTCTGCCCTGCCACC[C/G]CCACTCCATATTTAA | 83860 |
rs554972156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986655 | CATCTTGTAACTTCC[A/G]CTCAGCATCTTCAAG | 83860 |
rs554975567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7846159 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGACGG | 83860 |
rs555031648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998557 | AGAAATGTAGGAAAC[A/G]TAGGGAGAGGTGGGG | 83860 |
rs555036215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7840708 | ACCCCAAAGTTAGTA[C/T]TTTTGCTGTAAGTTA | 83860 |
rs555043383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827394 | CATAACAGTGGGCCA[A/G]GTGTGATGGCTTATG | 83860 |
rs555054901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936696 | ATCATAGTCAGCAGA[A/G]ACCACAGTTTACATT | 83860 |
rs555092301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8005102 | TTTCAAATCCACTAG[A/G]TCAAGTCACTCTCTG | 83860 |
rs555095585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834593 | GGATAGGGTTCCTCC[G/T]GAGTTCATGCAGATT | 83860 |
rs555097441 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847254 | TTCATATTTGTCAAT[A/G]TGAATTGACATATGT | 83860 |
rs555102665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7836559 | GATTACAGGCGTGAG[C/T]CACTGCACCCGGCCC | 83860 |
rs555127726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853337 | ATGTGGGGGCATTAC[A/G]TTGGCGGCTTGAAAT | 83860 |
rs555135750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877290 | GATCATCATTAAGGA[C/T]TGAGGTGGCAAGAAT | 83860 |
rs555161385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7898014 | GAATCTCTTGAACTT[C/T]TAATATTCTTATTTT | 83860 |
rs555164378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830731 | TCAAGTGATCCGCCA[A/G]CCTCGGCCTCCCAAA | 83860 |
rs555194444 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992156 | TGGCTTTGCTTTTTC[A/T]TAGTAAAAGCACCCT | 83860 |
rs555216178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870664 | TTAGGCCTTAACGAG[C/T]GGCAGAACTCGACAC | 83860 |
rs555218595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898694 | CCGCTGTGCAAAAGC[A/G]GAAAGAAAGAGGTAG | 83860 |
rs555223217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904586 | AACAAAGGAAGGAAT[A/G]AATAAAGGAAGGGAA | 83860 |
rs555228641 | snp | A/G | 1.65765e-05 | 0.00287888 | missense | TAF3 | GRCh38.p7 | 10:7964189 | CAAAAGATCCCACCA[A/G]TGCTTTCTCCAGTCC | 83860 |
rs555256334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7856399 | GCAGGAGAATCGCTT[A/G]AACCCAGTAGGTGGA | 83860 |
rs555277120 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7861559 | CTCAAAAAAGTCCAT[-/A]AAAAATGATTATATA | 83860 |
rs555328757 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868111 | GGGGTGGCAGAGGTG[A/G]GAGAAAATCCACATA | 83860 |
rs555365666 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7929586 | TGATTTTATAGACAA[A/G]CTCCTGGACTCAAGT | 83860 |
rs555403992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885167 | AGTGGTGATGGTTGC[A/T]TGACAGTGTGAAAAT | 83860 |
rs555423040 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876041 | AAATTTATATTTATA[A/G]AAAGGAAGTTTGTTT | 83860 |
rs555427418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899582 | GCAGCTTTGTGCTTG[C/G]TACTGGAAGGTTAAG | 83860 |
rs555452261 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7844381 | CTTCTTCTTGTTCTT[C/T]TTTTTTTTTTTTTTG | 83860 |
rs555455352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946965 | CGGATTCTCGCTACA[C/G]TGCCCAGGCTGGTCT | 83860 |
rs555456224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953386 | TGTCCTGCCCTTTAG[A/G]TCATCCCACACATGG | 83860 |
rs555464061 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960640 | GCATGGCTGGAATGG[A/G]TAGAGCACGCAGGGG | 83860 |
rs555497749 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7823580 | GTTTGAGGCAGCAAG[G/T]AGCTGTGATCATACC | 83860 |
rs555503785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7919127 | AAAAAAAATGGGAGA[C/T]TGAGTGCGACTAGGG | 83860 |
rs555505960 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:8001218 | GCTTGCACGTTTTTA[A/G]GTTTTCCATAATCAT | 83860 |
rs555531052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942386 | TTATCTCTGGTAGTT[A/C]AGGTTTTTTTCAGCT | 83860 |
rs555533420 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997773 | AGAACTTACTATGCA[A/G]TTAAACAGGAGAGAA | 83860 |
rs555543454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983169 | TGTTGTGATTCTTGG[C/T]GCTCACAGTCCCTGG | 83860 |
rs555551912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005993 | TGCCTTGGTTTCTTC[A/G]TTTAAAAAGCAGAAT | 83860 |
rs555555986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7900601 | GGGGCATGAAATCGA[A/G]TCTCAACTAGGAAAA | 83860 |
rs555597650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934602 | AGCACCCGCCACCAC[A/G]CCTGGCTAATTTTTG | 83860 |
rs555631827 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7976264 | CTTTTTTTTTTTTTT[A/T]AAGATGGAGTCTTGC | 83860 |
rs555678220 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7965813 | GGTAAACAAAGCCCA[C/T]AATTATATCTGTATT | 83860 |
rs555691114 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7983581 | AAAACAACAACAACA[A/C]CACAAAAAAAGATTA | 83860 |
rs555707939 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TAF3 | GRCh38.p7 | 10:7842167 | TTTTTTTTTTTTGTT[G/T]TTTTTTTTGTTTTTT | 83860 |
rs555708283 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933820 | TCATCTTAAGCCTGT[A/T]CTTTGGCTATTATAA | 83860 |
rs555709767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7849915 | TGAAATCCTGAGCTC[A/G]GGCAGTCTACTCACC | 83860 |
rs555716741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858663 | TAATGAGAACTTATT[G/T]TAGGATTGCAGTGAG | 83860 |
rs555724885 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000969 | TATCATTTGTGTGTG[A/T]GCACACATGTGTATC | 83860 |
rs555742921 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8006550 | GCACCAACAAGCCTG[G/T]GCTAAAGTCTCTTGA | 83860 |
rs555774354 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7906134 | GAATATATATGTGAT[A/G]TTTCATCTCTTGTCC | 83860 |
rs555775693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7961910 | GCTGGAGTGCAGTGG[C/T]GCAATCATGGCTCAT | 83860 |
rs555780159 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957926 | TATTTTTGCAATAAC[A/G]TATCAAGATTAGATA | 83860 |
rs555781727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7851747 | TTTTTGGCATATCTA[C/T]GGTAGTATTATCACA | 83860 |
rs555797072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878695 | TAATTCAACCAATGT[A/G]TGTATGTATGTATGT | 83860 |
rs555808218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999562 | CCCAGGTTCAAGCAG[G/T]TCTCCCGCCCCAGCA | 83860 |
rs555808946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7857989 | GGGGGAGGTAGGAGT[A/G]GGGGAGAGTGGAATT | 83860 |
rs555817715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990927 | TCTCGAGCCCCTCTC[C/T]GTAGTCCTAGATGTT | 83860 |
rs555828761 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7851753 | GCATATCTACGGTAG[-/TAT]TATCACACCCTTAAA | 83860 |
rs555843195 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822299 | GGTTAGAAACTACCA[A/G]GTTTTGGTTTGAGGC | 83860 |
rs555884597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7831297 | CTAGTTTCATTTAAT[A/G]CTCTATCATTGTGAA | 83860 |
rs555890589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984633 | TTAGGTTTTAAAATA[G/T]TTATGACCACCTCTT | 83860 |
rs555919042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7919186 | CAGTTGGATGTCCTA[A/G]GAGGCCTAGCTTCTG | 83860 |
rs555928246 | snp | C/T | 3.31461e-05 | 0.00407086 | intron-variant | TAF3 | GRCh38.p7 | 10:8013852 | GGTGAGTGCCCAGGG[C/T]GCCCTGCCGGCCACA | 83860 |
rs555938682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886115 | TTTTTGTAGAGATGT[A/G]GGGGGGTCTCACTAT | 83860 |
rs555943515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870462 | AATTTATTTACGTGA[G/T]TGTTGCCTGATGGAA | 83860 |
rs555948397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891301 | CCTTGAGGTACTTTC[A/G]GGAATGATTAAGGTG | 83860 |
rs555983260 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944731 | GCCTTCCAGGGTATA[A/G]AAGAATTAGACAAAA | 83860 |
rs555984056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824194 | TCTATTAAATTCTTT[C/T]CAATAACTAGGTTAA | 83860 |
rs555995644 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942304 | AAAGATACTTAGGGT[A/G]AATATTTTATCAAAC | 83860 |
rs556001948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7924021 | AGTTGAAGTCTGTAG[C/T]TGACAGTATTTAGGC | 83860 |
rs556055461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864016 | GCTCCTTCATCCCCT[C/T]ATCCTTCCCCACTGT | 83860 |
rs556061622 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921428 | CAACTTTCTTTGATA[A/C]CTCCCCTCCCCCGTT | 83860 |
rs556076317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014356 | TTCAGTTATGATAGA[C/T]GATATCTGTGAGATA | 83860 |
rs556083715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7991761 | AGAATTCATATAAAG[C/T]ATGGTGATTTTGGTG | 83860 |
rs556118776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864501 | TATTCTTAACCGTAG[C/T]CACATTGCTATACAA | 83860 |
rs556126766 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960109 | CAAACCTTTATCATT[C/G]TGTTTTGGCATCATT | 83860 |
rs556143224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8000120 | CATTTTCATCTTTTT[C/T]GTTGTTTTGCTTTGT | 83860 |
rs556156732 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7852681 | ATAATATCATTTGTG[-/A]AATGTGTGGGTGTGA | 83860 |
rs556167923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7837538 | ATCTCATCTACTCGG[A/G]TGGCTGAGGCACAAG | 83860 |
rs556184526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967772 | ATTCTGAATCAAACT[A/G]TAAAATGTAGGAACC | 83860 |
rs556188274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934655 | TCACCGTGTTGGCCA[A/G]ACTGGTCTTGAACTC | 83860 |
rs556207761 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932252 | TGTGCACTAAAGGGT[A/G]GTGTCAGTTTTCACC | 83860 |
rs556213343 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959163 | ACACACACACACACA[-/CA]AAAAAAGTTTCAGGC | 83860 |
rs556243465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871080 | AATTAAAAATAGTAA[C/T]ACACTGTAGTCAGTC | 83860 |
rs556247175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941286 | TTACTGTTTGGCATC[A/G]AATAGGCATACAGTA | 83860 |
rs556264823 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:8014375 | ATCTGTGAGATAAAG[A/C]CAAAGCCGTGGCTCG | 83860 |
rs556265636 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888796 | CATTAGCCACGTTGT[A/G]CTTTTAAGATGACTG | 83860 |
rs556310252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7940547 | AAGTTAGAAACAGCC[A/G]TGGAGATTTGAGGAA | 83860 |
rs556329698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948727 | CATAACAACCAAAAG[C/G]TTAAATACTGATCTT | 83860 |
rs556332164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936371 | GGGAGATAAGACGGG[G/T]ATTTCTCTTACAGTT | 83860 |
rs556334217 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864272 | TGTGGCAACTACTGA[C/T]CATTTTATTGTCTCC | 83860 |
rs556350222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000194 | GAGTGCAGTGGCACT[A/G]TCTCAGCTCACTCCT | 83860 |
rs556360035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968409 | AATAAAGATGTGATT[A/G]ATTAAAACGGAATTT | 83860 |
rs556397411 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986169 | CTTTTTGCCCTTGGT[A/T]CAGTAACTCTGTTTC | 83860 |
rs556411470 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969964 | CTAAAGTTTAACTTA[C/T]CTCTGCTTAAAAACA | 83860 |
rs556413460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006628 | AAATAGAGAACAATT[C/T]GACAGCAGTAATGAA | 83860 |
rs556421452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976082 | TGATTATATGATCTG[C/T]AAACCAACAATTGTG | 83860 |
rs556422652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907302 | GATTGTGATGCCAGA[C/T]GAGGTCTTTGAAATC | 83860 |
rs556431588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7843335 | ACTGGTCTTGAACTC[C/T]TGGGCTCAAGCGATC | 83860 |
rs556466314 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823824 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 83860 |
rs556502480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7976874 | TTTATCTTATAGGGA[A/G]GACATCATCGCAGTT | 83860 |
rs556505109 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911686 | TTTGTCTCATGTTGT[C/G]TATTTTAAAATTCTG | 83860 |
rs556525710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000567 | AGTCCAGGAGTTCCA[G/T]ACCAGCCTGGGCAAC | 83860 |
rs556526339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7935172 | ATCCCAGCTACTCAG[A/G]AGGGTGAGACATGAG | 83860 |
rs556534947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7943109 | ATCCTGCTCAGATCA[A/G]AGGAGTCCAATCCTG | 83860 |
rs556551477 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913328 | AGGGTTTCTTTGAAA[C/T]GCAGGATGTGCCTGG | 83860 |
rs556562559 | in-del | -/AT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850682 | CCATCTCAAAAAAAA[-/AT]AAAAATATATATGTA | 83860 |
rs556563596 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863156 | GACAGCATTTCAGAC[C/T]CTTTATGATTCTTGA | 83860 |
rs556575710 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938246 | TTGGGAGTTTGGTGT[A/G]GCTAGGGATGGGGAG | 83860 |
rs556588950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8007443 | ATACCTGTCTTAGGG[C/T]AGTGGTTGCTCTGGG | 83860 |
rs556636527 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962601 | TTCTCTTACACTCCC[C/T]GTGTTTCACCTTCAT | 83860 |
rs556640462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7935963 | AGAGCACTCTCGAGT[C/T]TCATTTGGGCTGCCG | 83860 |
rs556642418 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7955619 | CCTAATGTCTATGAA[C/G]TTTTTAGATTATAGT | 83860 |
rs556659388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951694 | ATTTTTACAGTCTGA[C/T]TCGTACTTCTCATAC | 83860 |
rs556664968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886839 | TACAAAATTAATAGA[A/G]AAAATATAGACTAAT | 83860 |
rs556678571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7977758 | ACATGGTTTTATTCT[C/G]TACCTGTAAAACAAA | 83860 |
rs556685663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8003652 | ATTTAATGCAGCATT[A/G]AAGAAGAACTTACAC | 83860 |
rs556690235 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7981991 | AAGAATAATCATGGG[A/C]AGTTACAAAAATAAT | 83860 |
rs556691842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7896973 | TGTTCCTGGCTGGCC[A/G]TGAGCCAGCAGTTGT | 83860 |
rs556698597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915850 | TGGATTTGGTGGTGG[A/G]CACCTGTAATCCAGC | 83860 |
rs556702609 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892111 | ATTAGTGTATTTACA[A/C]CTTTATGCATTACAA | 83860 |
rs556704025 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TAF3 | GRCh38.p7 | 10:7954848 | CTCCATAGTGAGATT[C/T]AGAGTGCACTCCATA | 83860 |
rs556705796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7962439 | TCTGTTGTCTAAAAT[C/T]CTTCTAGGTCCAAAC | 83860 |
rs556715539 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890483 | AAGCATGCAATTGTT[C/T]AAAGAAGAAAAGATT | 83860 |
rs556726482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887209 | TGCACTCCTGCCTGG[C/G]TGACAGAGCCAGACT | 83860 |
rs556726800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7847771 | TTGTTAAAACTTCTT[G/T]TTTTCTTAATTTTGA | 83860 |
rs556728249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879944 | CTGGGCACGATGGGT[A/C]ACAACAGTAATCCTG | 83860 |
rs556743454 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875030 | GATACTCAATTATAG[A/G]TAGCAGTTTGTAGGT | 83860 |
rs556747435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010283 | ATCACAATGTTCACA[A/T]AGTCAGCCTCCATAA | 83860 |
rs556753507 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932399 | GATAGCACACATGCC[A/G]GAAGTACTGATTCAG | 83860 |
rs556762141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916827 | CAATGGTGCTTTTCA[A/G]TTTACTTACTATCTG | 83860 |
rs556762188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909476 | TGGACTTCACTGTGC[C/T]ATTGGATAAACTAGT | 83860 |
rs556790863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938558 | AACGGCCAGTCAGAC[A/G]AAAAAAAGAAAACGT | 83860 |
rs556811961 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7985877 | CAGCCTCCGCCTCCT[C/G]GGTTCAAGTGATTCT | 83860 |
rs556823174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910319 | AGAAAATACTGCTAC[A/G]ACATACAAACATCTA | 83860 |
rs556836337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942524 | TTACCCATAAAATTA[C/T]AAGCTTTGCTTTCTG | 83860 |
rs556838700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858736 | TCACATGCTTAGCAC[A/G]TGTTAGCAGCTATGA | 83860 |
rs556873292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7993817 | CTGAAATTCATCCCT[A/G]AAGGTGAACCTCAGC | 83860 |
rs556898300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821087 | TCTATGTGACTAGGT[A/G]TTCCAAAGTCATCCA | 83860 |
rs556900167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7851839 | ACTCAAGCTGGAGTG[C/T]AGTGGTACAGTCCTG | 83860 |
rs556900253 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7859154 | TAGTCCCAGTTACTC[A/G]GGAGGCTGAGGCAGG | 83860 |
rs556938774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992782 | TTTTTATTAATATTT[G/T]CAAACATAAAAGAGT | 83860 |
rs556981735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002788 | AGATAAATATGCTTA[C/T]ATCTGTGGCTATGAT | 83860 |
rs556995499 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882819 | TTCAGACTTACAGAA[A/G]AGATACAAGAATAGC | 83860 |
rs557026577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7848795 | TTGGCATAAACTTTA[C/T]GCCAATATGCCTTTA | 83860 |
rs557034200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958880 | TGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG | 83860 |
rs557065067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889589 | TGTATGCCTCCTGTC[C/G]CTTCCTCAAGCCTTG | 83860 |
rs557119104 | in-del | -/TATTGTTAGTTGAA | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7921769 | CCAAATGGCTGATAT[-/TATTGTTAGTTGAA]TATTGTAGAAGAAAA | 83860 |
rs557124506 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7883114 | CTACACTGAGATTAC[A/G]TCAGTTGTCCCAGTG | 83860 |
rs557139640 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836990 | CCCAGCACTTGGGAG[A/G]CCAAGGCAGGAGGAT | 83860 |
rs557172829 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955563 | TGTAGTTAGTCAGAT[A/G]AAAAGCTTCTATGCC | 83860 |
rs557174030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973639 | TGTTTTTTAAAAACC[C/T]TAATGAGCACATTGG | 83860 |
rs557176448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946266 | CTCTTGCCTTCACCT[G/T]CTCCTTCCCATGCCT | 83860 |
rs557184909 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980378 | GAGCTTGGATTGTTT[C/T]CTGTGTTCCCTATTA | 83860 |
rs557185323 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954097 | AGCTCTCCATAGTGA[C/G]ATTTAGAGTGCACTC | 83860 |
rs557216273 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861365 | CCCACCTTGTCCTCC[C/G]AAAGTGCTGGGATTA | 83860 |
rs557223015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898813 | TCTTTGTTTTCTTTG[A/G]GTTTTTTTTTTCTCT | 83860 |
rs557224342 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983172 | TGTGATTCTTGGTGC[C/T]CACAGTCCCTGGCGA | 83860 |
rs557243951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854905 | GCAAAAGTGGTATTT[A/G]TTAAACACTTTTGAC | 83860 |
rs557248494 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978532 | TTCGGTTGTGCCAGT[A/G]GAGACCTAGGAAATG | 83860 |
rs557249242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7861381 | AAAGTGCTGGGATTA[C/T]AAGCATGAGCCACCG | 83860 |
rs557251536 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7947244 | TGCTGTGCAATCTGC[A/C]GGTCACCTTTCCTGC | 83860 |
rs557273994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998729 | CCTCAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 83860 |
rs557275495 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906693 | ATGAAGGAACCAAAC[A/G]AATTAAATAGAGCGC | 83860 |
rs557278310 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949068 | TCAACAGTGTCAGGA[C/T]GATTTCCCATTACTT | 83860 |
rs557287492 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884261 | CTCAAGCTCCCTCCT[A/T]TGTCCTTAGGCATGT | 83860 |
rs557318885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869418 | ATTTGGGTTTTCTCC[C/G]CAGCTTATTTTATTG | 83860 |
rs557327205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926519 | AACAAAATGTTCTTA[C/T]AAGACTTTATGAGAT | 83860 |
rs557328815 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859080 | ATCCTGGCTAACACG[A/G]TGAAACCCCGTCTCT | 83860 |
rs557333865 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:8005199 | TGTTTTATAGTTGAT[A/T]ATTCTTGTATCTGTG | 83860 |
rs557340196 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991855 | ATGACTTCAGTAATA[A/T]CTGAATTTTATAACT | 83860 |
rs557350807 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880996 | ATCCCAGCACTTTGG[A/G]AGGCTGAAGCTGGAG | 83860 |
rs557355676 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8003856 | TTCAAGACCACCCTG[A/G/T]GCAACAGAGCAAGAC | 83860 |
rs557379920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011262 | TTTTTTTATGTTTTC[C/T]TTTTTTCTTTTGAGG | 83860 |
rs557388469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868650 | AATCTCATTTCCTCT[C/T]ATGGAAAATATAGAT | 83860 |
rs557398070 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:8004323 | AAAGTGCTGGGATTA[C/T]GGGCATGAGCCAATG | 83860 |
rs557451821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946306 | AACTCGTTACGCAGT[A/G]TGGCTGTCCACATGC | 83860 |
rs557457692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8011026 | TGTTTATACAGATTA[C/T]GTTCTTTGGATACTA | 83860 |
rs557472265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7997465 | CTGGGGAGGTGAGGA[C/T]GGGCTCTTTATTGAC | 83860 |
rs557474115 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913100 | CCTCTCCGCACACAC[A/G]CCCGTGATGTCTCTC | 83860 |
rs557474391 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960281 | GAGCAGATCTGAAGT[C/T]CGCCTTGTCATTCTG | 83860 |
rs557478397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7890462 | TTAATCGCAGAAAAG[A/G]AGTTTAAGCATGCAA | 83860 |
rs557481695 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816905 | TTGCAGCTTATTTTC[A/G]AACTGCTGGAAAAAA | 83860 |
rs557507520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954140 | AATGAATTAGTCCCA[G/T]TTAACACAGAGCTCT | 83860 |
rs557515682 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930123 | GGATCACTTGAGCCC[A/C]GGGAAGTCAAGACTG | 83860 |
rs557525104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925875 | TACAATTTCAATACC[G/T]TGATTAATTTAATTG | 83860 |
rs557540567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905678 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 83860 |
rs557583459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883624 | CATATTAATTATTCC[C/T]AATAGTTGCTGGATG | 83860 |
rs557587816 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016815 | CATTTAAGGAATTTC[A/G]ATCAGTTTGTTGTCC | 83860 |
rs557683400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917748 | GATACGGGGTGCGAG[A/G]AGAAGAGAGGAAATG | 83860 |
rs557706299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857194 | ATGAGTGACTTTTTT[C/G]CTGAATTGGATACTA | 83860 |
rs557753120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7848973 | GAGACTTTCCTTTTT[C/T]AGCTTTGTCTTTCTG | 83860 |
rs557753389 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835162 | ACACTGGAAGAAGAA[C/G]GATTGTCTTTGGCCA | 83860 |
rs557804022 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859394 | TTCTGAGTTTCAGGA[A/G]GGCAGCGGGGATTTC | 83860 |
rs557807013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891039 | GAATTGGGGCCCCGC[A/C]CTTTGCATGTCTGCA | 83860 |
rs557848467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7982625 | GACTGGTCTCAAACT[C/T]CTAACCTCCGGTGAT | 83860 |
rs557861156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883694 | TTGGCATTCTACTCT[A/G]TGGAAGATTTTCCCC | 83860 |
rs557862447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8003750 | TTGCAAAAATTTAAA[A/T]CATTGCCAGTCTTGG | 83860 |
rs557862455 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883230 | TTAGTTCTTCAATCT[A/G]GAACAGTTCCTCAGC | 83860 |
rs557863624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926633 | AGTTCTTTTAAAATC[A/T]GTATAATTACTCTGG | 83860 |
rs557863654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7856223 | GGCGCAGTGGCTCAC[A/G]CCAGCACTTTGGGAG | 83860 |
rs557872299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884443 | CCAGGTTGGAGTACA[A/G]TGGTGCCATCTCGGC | 83860 |
rs557876315 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7937604 | TCCTTTATCAGATAC[A/G]CCTTGTAAATATATT | 83860 |
rs557882405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829871 | TAGGAACTCTTCTGC[A/G]TGGGGATTTCTCTCT | 83860 |
rs557888159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7983082 | AGGCTTGCCAAGTAT[C/T]CTAGGGCTCTGCCCA | 83860 |
rs557898256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951768 | ACTGTTACTCAAAAG[C/G]CAAAGAGGTAGTACT | 83860 |
rs557922768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876620 | CGTATACAGAATCAC[A/G]GGGGTCAGTGGTTAT | 83860 |
rs557952600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973835 | CTCTTCATTTAAAAA[A/G]TATATTGGAGACAGC | 83860 |
rs557967788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7966821 | CAACTCCCATTTTTC[A/G]CCTACCTTGATTTGT | 83860 |
rs557974983 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7862789 | CATGGTATGTACTGT[G/T]TTTTGGTCTGGCCTT | 83860 |
rs557993483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986870 | GATCTGAGAAGCAAA[A/G]CACTTAAAAGTCTGA | 83860 |
rs558009792 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816534 | TTGCCTGAGAGCACA[C/T]ACCCTTTCCCAGGTA | 83860 |
rs558027059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855979 | TTCTCTACTAGTATT[C/G]TAAGAGAGGACAAGA | 83860 |
rs558036112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7954229 | ACAGAGCTCTTCCTA[A/G]TGAGATTCAGAGTGC | 83860 |
rs558093005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827135 | GGCGAGTGTGCACAC[A/G]TAGAAGGCCTGAAGG | 83860 |
rs558102523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961321 | AGCATAATTGATGAG[A/G]TTGTGATGTTCTTTA | 83860 |
rs558103571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956441 | GCAGTGAACCGGAAT[C/T]ATGCCACTGCACTCC | 83860 |
rs558109417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860475 | GTGCACACATTTTAT[A/G]TGTATTATTTTATGA | 83860 |
rs558110656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864005 | AAATTCATCCTGCTC[A/C]TTCATCCCCTTATCC | 83860 |
rs558116588 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990919 | TGGAAACTTCTCGAG[C/T]CCCTCTCCGTAGTCC | 83860 |
rs558120192 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7869569 | CACTATTTTAACAGT[A/G]CTTTTATTAACATTC | 83860 |
rs558123578 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839286 | TTCATATATTTTGTT[A/G]TAATTGCTGGTTTTA | 83860 |
rs558146523 | in-del | -/TTGTTGT/TTT | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7838375 | TTTTTTTTGTTGTTG[-/TTGTTGT/TTT]TTGTTTGTTTGTTTG | 83860 |
rs558151037 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927136 | GTCCTCATTCAGAGA[A/G]CACTTTCTGAGTTAA | 83860 |
rs558171904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857814 | GGGGAAAATTAGAGA[A/C]GTTATGAAAGTACTA | 83860 |
rs558173117 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7860891 | TGCAACCTCTGCCTC[C/T]TGGGTTCAAGCAATT | 83860 |
rs558181837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7863408 | CTGAGTTCAGGAGTT[C/T]GAGATCAGCCTGGCC | 83860 |
rs558192654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8005329 | TTTTTTTTAAAGATA[A/G]TTATCTGTATTAATA | 83860 |
rs558192928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012632 | GGTTCTCACCCCTTG[C/T]TACTTTTTCTCCTGG | 83860 |
rs558200949 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7905895 | CTAAAAAAAAAAAAA[A/T]TTAGCAAAGATTCTG | 83860 |
rs558203866 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816946 | TGCATATATAAATAC[A/C]AAATATATAGTAAAT | 83860 |
rs558208254 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:8009687 | AATGCGGTGGTGAGA[G/T]CTCAGCTCACTGCAA | 83860 |
rs558224416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915216 | AAGTGCTGGGATTAC[A/G]GGCAGGGCATGAGCC | 83860 |
rs558234196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854139 | ACTGAAATGATTCAA[C/T]CCCTTGAATGAGATA | 83860 |
rs558247083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866148 | TTTCTAAGTTCCTCC[A/G]GTATGCATATGTTCC | 83860 |
rs558256370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8011909 | CTGGCTGTGCATGGT[A/G]TCTCACGCCTATAAT | 83860 |
rs558261067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929456 | AACTAGGCTGGAGTG[C/T]TCCTGATCTTGGCTC | 83860 |
rs558262292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899497 | AGTGTTTCTTTCCCT[C/G]TACAGTTAAACCCAG | 83860 |
rs558299974 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827487 | CCTCATCTCTACTAA[A/T]AATAAAAAACTTGGC | 83860 |
rs558303828 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7832984 | GAGGATGATTTGAGG[C/G]CAGGAGTTCGAGATA | 83860 |
rs558382230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877106 | CTTTCTTGGATTTTT[A/G]AAATACTTTTTACTT | 83860 |
rs558401913 | in-del | -/TA | 0.0368353 | 0.130617 | intron-variant | TAF3 | GRCh38.p7 | 10:7916637 | TTTAAAAATAAAGTG[-/TA]TATATATATATATTT | 83860 |
rs558429293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826324 | TAGCATGCAAATATT[C/T]CATAATAAAATTCTC | 83860 |
rs558476949 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865992 | CGGCACCTTGACTTT[C/T]GTTTTACCCAATAGC | 83860 |
rs558488960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819669 | AATAGAAGCTCCACA[C/T]TATCTTGTTGATGTG | 83860 |
rs558525543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875141 | TATGTATTCTTTATC[A/G]GTCACTATTTATATG | 83860 |
rs558546183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908321 | GGTGACTCTTCCCAT[A/G]CAGGAATGCAAGCCC | 83860 |
rs558550365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7979460 | CTGTTTTCCCCCTCA[A/G]TAAATCACTCATACA | 83860 |
rs558576353 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016427 | GGTGTCATTGCCCTC[A/G]TTGTTCAAGAGGCCA | 83860 |
rs558586494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875700 | TCCTTTTAAAATATA[C/T]CTAGTTTAGTGAATT | 83860 |
rs558599136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873646 | TCAAAAGGGGGTGTC[A/G]AATTTGAGGGGAGTC | 83860 |
rs558606309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987352 | CTTAGAATTATCTTA[C/T]ACATACTGTTCAGCA | 83860 |
rs558607756 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7908916 | TCTGAGTCAGTGGCC[C/G]TGGGATGGAGCCCAG | 83860 |
rs558617015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970110 | ACTACAACAGTTCCT[A/G]AATTTTCATACACAT | 83860 |
rs558667965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895664 | GATTCTAATTGAAAA[A/G]GGCCTGGGCTTTGGA | 83860 |
rs558717507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010364 | ATATACAGTAATATC[A/G]ATCTGTAAATGTAGA | 83860 |
rs558730479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7902828 | TTCTATCACTTCTGT[A/G]TTGAAATTCTTCCAT | 83860 |
rs558766264 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903345 | GTCCATCTCAGCTTT[G/T]GAACATTTTCTTACT | 83860 |
rs558774075 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7872852 | AGACATATATGTTAT[A/G]TAAAATAACATTAAA | 83860 |
rs558781355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880468 | TCCTGACTAGCACCC[A/T]GAGAAAACAGTGTGC | 83860 |
rs558798996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7867826 | TGTAACTTTTGACTC[C/G]CCCAAAACTTTACTA | 83860 |
rs558816727 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7835949 | CAGGATTCCCCTTAT[G/T]GAAGCTTTTTGCTGC | 83860 |
rs558827558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995667 | TTGTTTCATTTTTCA[A/T]ATAGGTCATGCCTGC | 83860 |
rs558830296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865624 | GCTGGCTTTAGCAGC[C/T]CCGGCAGGGTGGATG | 83860 |
rs558858211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7882102 | GCTATTTCCTATACT[C/G]ATGCATTATAAATTG | 83860 |
rs558915296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846797 | TTATCATTCATCATT[A/G]CTCATCAGTTATTTC | 83860 |
rs558919040 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839957 | TACAAATTTAAATGG[A/T]CTTTGCCAAAATTCT | 83860 |
rs558920656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008777 | GAAGCCGTCAGAGCT[G/T]CTGCCCCAGCACAGG | 83860 |
rs558929540 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014542 | GATTTCGGGTAAACA[A/T]GTCATAGACTCTAAA | 83860 |
rs558962047 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7867244 | AGCCTGGGCAACAGA[A/G]TGAGACTGTCACACA | 83860 |
rs558962954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950009 | TTAGAGTCAATGATA[C/T]ATGGTGAAATCGTTT | 83860 |
rs558970938 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7846242 | CATTACAGGCATGAG[C/T]CACTGCGCCCGGCCA | 83860 |
rs558983242 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7972625 | TACCTGTTGCCTTCC[A/G]GGCACATTTATACCA | 83860 |
rs558985031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821247 | ATGCTAATTTTGGTA[C/T]ACTTATTAGATATTT | 83860 |
rs558986352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931312 | TGCTGATCAATGGCA[A/G]ACTTGGTCCTTGAAC | 83860 |
rs559000852 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869060 | ATACATCGTAGAACA[A/G]TTCCCTATTTTGCTT | 83860 |
rs559006822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835160 | TCACACTGGAAGAAG[A/G]AGGATTGTCTTTGGC | 83860 |
rs559031794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7840310 | GGCGCCCGCCACCAC[A/G]CCTGGCTAATTGTTT | 83860 |
rs559050049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937970 | GGAAATGGGGTTTAT[A/G]TTGAGGGCCGCTTAG | 83860 |
rs559069927 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828451 | AGTGAGACCTCTTTG[A/C]AAATATTTTATACAT | 83860 |
rs559074068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846213 | CTGCCCGCCTTGGCC[A/T]CCCGAAGTGCTGGCA | 83860 |
rs559074320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7971038 | AAAACAAGAAACTTA[A/G]TGTTTAAATGAGTAT | 83860 |
rs559074590 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877565 | TGAGAATATGGCATT[C/T]ATTGTTAGAATTTTC | 83860 |
rs559093095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828705 | ATGGGGGTCTTCTGG[A/G]GGGGTCTGTTGATTG | 83860 |
rs559114480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937452 | GTGGAACATCTTTTC[A/G]TCTTTTCCTGTGCCT | 83860 |
rs559138141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978996 | CAGTGAGCTATGATC[A/G]TGCCCACTGCACTCC | 83860 |
rs559145725 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823697 | TAGAGTGTAGTGGCA[A/C]GATCTCGGCTCACTG | 83860 |
rs559150971 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001196 | GAAGTGGAATTGCTG[A/G]TAAAGAGCTTGCACG | 83860 |
rs559159486 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904517 | ATCTCATATTTGTTG[A/G]ATAATTAAATGACTG | 83860 |
rs559182924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852945 | CCAACTAGTTGTGCA[A/T]ATGTTTTTTGAAAGT | 83860 |
rs559198841 | snp | A/C | 1.66236e-05 | 0.00288297 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964783 | TTTACTAGCCCTAAG[A/C]GAATTTCAGGCCCGG | 83860 |
rs559199563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978403 | ATGAATGTGAGCAGA[A/G]AGGCAACTTGGTTTT | 83860 |
rs559223729 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7881587 | ATATCAAATAGGTAT[A/T]TGTTTTACAAATAAA | 83860 |
rs559248558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7914862 | TAGCCTTTTCCTTGT[A/G]TATGATAAACACATC | 83860 |
rs559251205 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830516 | TGAGAAGGAGTCTTG[C/T]TCTGTCACCCAGGCT | 83860 |
rs559275953 | in-del | -/TGCCTGTAGTCTCA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012049 | GGGCAGGGTGACATG[-/TGCCTGTAGTCTCA]ACTACTCAGGAGGCT | 83860 |
rs559311289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994311 | AGCAATTTCTCCAAG[A/G]AACATTGGTTCCTTC | 83860 |
rs559320958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7849460 | GGACGATTTAGGGTT[A/G]TTGCATGGGATGTGT | 83860 |
rs559324690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931936 | TGAAATAATAGAAAT[G/T]TACTGGGTCTTGAGG | 83860 |
rs559324747 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847704 | CCCACCTTGGCTTCC[C/T]AAAGTGCTGGGATTA | 83860 |
rs559346789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895099 | CAGGCTCCTGACCTT[C/G]GGTGATCCGCCTGCC | 83860 |
rs559347518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7839640 | ACAAAGGCTTGTATT[A/G]TGGCTCTTCGTTTGT | 83860 |
rs559357691 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999617 | GGATACCACCATGCC[C/T]GGCTAATTTTTGTAT | 83860 |
rs559379144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880999 | CCAGCACTTTGGGAG[C/G]CTGAAGCTGGAGGCT | 83860 |
rs559409585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895716 | ATTTTTTTCCACTAA[C/T]TGTGTGGCCTCTATC | 83860 |
rs559412768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7971964 | GTTACCTACAAAGGA[G/T]TCTTATATTGCTGGA | 83860 |
rs559453746 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7909751 | ACCACTTTATATCTT[C/T]ATAAAGGTATCTTTA | 83860 |
rs559462995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907895 | GGCAGGAGCTAGTGA[A/C]GTGGGCTCTGTGACA | 83860 |
rs559515120 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969882 | CAACCTCCCATCCTC[A/G]CAGACCCTCTGCTTC | 83860 |
rs559515202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903422 | GTCTCAGCCTTGGAA[A/G]CAACTCTTTCTCCAG | 83860 |
rs559523130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7874270 | TCTGCATTTAAACTT[C/G]TACTGATGAAGTTTT | 83860 |
rs559526233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008353 | ATCCACCCACCTCGG[C/T]CTCCCAGAGTGCTAG | 83860 |
rs559527863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000941 | TTACACCTCCCTTTT[G/T]CTTGGATAGACATAT | 83860 |
rs559530976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996657 | GGGGTTTTTTTTGTG[G/T]TATCTGTATTCTTAC | 83860 |
rs559549209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7929799 | GGCTTTAATTTTACA[A/G]TGGTTCTAAAGTGGT | 83860 |
rs559550583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855316 | CTGCCTCTACAAAAG[A/G]CTGACTTCAAAGGGC | 83860 |
rs559585513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865646 | GGGTGGATGCAGCCA[C/T]GTGCAAAGTAGCAAC | 83860 |
rs559590142 | snp | A/G | 0.000803697 | 0.02003 | intron-variant | TAF3 | GRCh38.p7 | 10:7996027 | TCTTCCAACTTCTGA[A/G]TATTTATTTACATAC | 83860 |
rs559590157 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:8003884 | GACGCCATTATCAAA[A/G]AAAAAACAACCAAAA | 83860 |
rs559611559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936913 | AATTTTACCTTTCCC[A/G]GAATGCCATAATTGG | 83860 |
rs559612561 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979158 | GACCATCCTGTCTAA[C/T]ACGGTGAAACCCCTT | 83860 |
rs559647028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986299 | AATCTGCCAAGTTAC[C/T]GGAAAGTTCTGCCTG | 83860 |
rs559656629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8003190 | GTGCTACTTCTTTAG[C/T]GTTCAGTGGTTTTTT | 83860 |
rs559661890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834377 | TGAGTTGATTTTTCT[A/G]AGTGGTATGAGATAA | 83860 |
rs559662390 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837017 | GGATCGTTTGAGCCC[A/G]GGAATTTGAGACCAG | 83860 |
rs559674362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901980 | GTGTGTGCACGTGGA[C/T]GCTCCTCCAGACTTT | 83860 |
rs559675664 | in-del | -/ATTA | 0.00199481 | 0.0315187 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015935 | TCTACAAATCTGTTC[-/ATTA]ATATTGTGCTTTAAG | 83860 |
rs559676318 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7976571 | AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTTT | 83860 |
rs559686551 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002620 | ATTGGGTCAGTTTCT[A/T]TCATTGTTCAGTATA | 83860 |
rs559697121 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916201 | GAGCTAGACAGTTTC[C/G]TTTGTTAATGGATTA | 83860 |
rs559721569 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7941512 | AGAGTTGAGTGGGCC[A/G]TGTAGTAATCAAGGT | 83860 |
rs559727095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957528 | TTTTCAGAATACTCT[A/C]AAGATAAATGGTGTT | 83860 |
rs559740592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7821356 | TCCACCCCTTTAAAT[A/C]CTTTCTGTTGTTTTA | 83860 |
rs559757182 | snp | A/G | 5.11509e-05 | 0.00505696 | missense | TAF3 | GRCh38.p7 | 10:8009160 | CCACCGCCGGCCCCC[A/G]CGCCCGCCCCCGGCC | 83860 |
rs559803623 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824951 | ATGAGTTGAATGCCA[C/T]GGCTTTATACTGGAA | 83860 |
rs559808613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975480 | TGGTAAACAGCTAGT[A/G]TTGGAGGCATACATG | 83860 |
rs559822031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855993 | TCTAAGAGAGGACAA[A/G]AAAAGATAACCAGGA | 83860 |
rs559823748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7846246 | ACAGGCATGAGCCAC[C/T]GCGCCCGGCCAAAAG | 83860 |
rs559898000 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877257 | TTCTAAAAAGCTACC[C/T]GACTTTGTGACTTTG | 83860 |
rs559899578 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984238 | ATTTAGTTTTTACCC[C/T]GGCACAATACTGTTT | 83860 |
rs559909875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7847396 | GAGAGTTTAAAAATA[C/T]TTTATGCTGTTAAGC | 83860 |
rs559910107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987819 | GAAATCCTTTCTTCT[G/T]TGGGGGAAGCTATTG | 83860 |
rs559916752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877732 | GACCCATTGTGATGA[A/G]GTGACTTGGCCAAGA | 83860 |
rs559918763 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894252 | TACAAATTCTCCCAT[A/G]ACGGAGTTACTGTCA | 83860 |
rs559921554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961091 | TGCACTGGAGGCCGA[C/G]ACTAGGTAGAAGGTC | 83860 |
rs559923238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8000240 | TCTAGCCTCAGCCTC[C/T]TGAGTAGCTAGGATT | 83860 |
rs559959259 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948187 | CTGGCCCCAGCCTCC[C/T]GAGTAGCTGGGTCCA | 83860 |
rs559959276 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TAF3 | GRCh38.p7 | 10:7911194 | GATCAAAACTCACTT[C/G]TTTAGAAAATAGAAA | 83860 |
rs559962862 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924564 | ATTTTCTCTTTAACC[A/T]TTCCTAACACGGAAC | 83860 |
rs559980104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878265 | GATTCAAAGGCCTGT[C/T]AGTAGTAGACTGGGT | 83860 |
rs559984090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006733 | AGTCAGTGCCTTTTG[G/T]TGAAAGTGGTTTCTA | 83860 |
rs560019054 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972232 | TGATTGTAGGAAATG[C/T]CTCTGTTTTTATTTT | 83860 |
rs560026263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945489 | TTTCTCTACCTGCCT[C/T]CCTTGGTATCTTCCC | 83860 |
rs560026439 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922215 | TGAATTTGTTTTTGC[C/T]CATTGAATAAGCAAA | 83860 |
rs560026497 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7915461 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 83860 |
rs560028026 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7998834 | ACAGAGTGAGACTCC[A/C]TCTCAAAAAAAAAAA | 83860 |
rs560029558 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7861207 | CTGACCTCGTGATCC[A/G]CCCGTCTTGGCCTCT | 83860 |
rs560030514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951990 | GAAAGGAATTGCAAT[G/T]AGATTAGTTTCATCC | 83860 |
rs560087773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012925 | GGAAGTTACCTTTTT[C/G]TTATTGCTGGTGTTG | 83860 |
rs560090821 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | TAF3 | GRCh38.p7 | 10:7920330 | TGTGTGTGTGTGTGT[A/G]TATGTGTGTGTGTGT | 83860 |
rs560093630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864237 | GTGTTCTACCTATTC[C/T]TCCCTCCCTTACCCC | 83860 |
rs560100358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991175 | TAGATACATACATAT[A/G]TATGTATAGATACAC | 83860 |
rs560103812 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817794 | GTCCCCATCCCCCGA[C/T]AGGTCACAGCCGCGA | 83860 |
rs560128797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7918879 | GCAGGTGGAAGGAAG[A/G]AGGGAAAATAGTCTA | 83860 |
rs560142272 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942734 | CCCAAGTGGGCAGCC[A/G]AGGCGTGTGGGCACG | 83860 |
rs560161364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999739 | TGGGATTACAGGCGT[G/T]AGCCACCGTGCCCAG | 83860 |
rs560189933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912348 | CAAGCGATCATTCTG[C/T]GTTGGCCCCGCAAAG | 83860 |
rs560240667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968768 | CAATCCAGGCTGTCA[C/G]ATGCTATAATTTATG | 83860 |
rs560286960 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890594 | TCTTTCTGTGAGTGT[C/T]GATTGTCTGATTAGA | 83860 |
rs560332251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842410 | ACCAGTCTTCCAGCG[A/T]TGGCCTCCCAAAGTG | 83860 |
rs560361866 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948832 | TTGTTTTTCTTTCGA[A/C/G]TCTTGCTTCCTAACA | 83860 |
rs560386659 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7969232 | CTCAGCTGCTTGGGA[A/G]GCTAAGGCGGGAGGA | 83860 |
rs560398006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919204 | GGCCTAGCTTCTGGC[A/T]AAGGTAATGGGGGAT | 83860 |
rs560417397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830882 | GATCTGCAGAGTGCC[C/G]CACAGTTGGATGTTG | 83860 |
rs560429377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948126 | GGAACGCAGTGGTAC[A/G]AACATAGTTCACTGC | 83860 |
rs560437236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928749 | CTGGGGCCCTTTCTC[A/T]TATCAAGTAATGCAG | 83860 |
rs560439067 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840298 | GCTCTGACTACAGGC[A/G]CCCGCCACCACGCCT | 83860 |
rs560456570 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7972185 | TCCTTTTGTTTGTTG[-/T]TTTTGGTAAGTGCAT | 83860 |
rs560463620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7831504 | GCATGTGCCACCACG[C/T]CCGGCTAATTTTTGT | 83860 |
rs560490913 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7871673 | GGTCTTGAACTCCCA[A/G]CCTCAGGTGATCTGC | 83860 |
rs560515013 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015728 | AAAGGGCCCGAGCAG[C/T]TGGAAGGAAAACAAG | 83860 |
rs560530721 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995690 | ATGCCTGCATTAAAA[A/G]ATAAAATGTTTGCTA | 83860 |
rs560533004 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895701 | CTTTCCATTGCACAC[A/G]TTTTTTTCCACTAAT | 83860 |
rs560534946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872295 | AAGTGTTTTTTAAAA[A/G]CAATGTTCTCTGTGT | 83860 |
rs560556977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991119 | AATTTCAGTCGTCTC[A/G]TCTTGCCTCAGAGAA | 83860 |
rs560575209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962114 | CCTCGGCCTCCCAAG[A/C]TGTTGGCATTACAGG | 83860 |
rs560581998 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7935575 | AGTGACAGAGAGAGA[C/G]AACGTCTCAAATAAA | 83860 |
rs560618765 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7984192 | ATTACTGTCTTATTT[C/T]TACCACCTAGAACAA | 83860 |
rs560647990 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7843960 | TAGGTGGCACTCTTT[A/C/G]AATTTCTGTTAGTGT | 83860 |
rs560660266 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7886892 | TACCATCTCTAAGAG[G/T]ATCTTTAAATTTTAT | 83860 |
rs560672305 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7937830 | CTAGAAAAGGGGTAC[-/T]TTTTTTATGCTCTTT | 83860 |
rs560707089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7844562 | TTTTGTATTTTAGTA[G/T]AGATGGGGTTTCACC | 83860 |
rs560750221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7993060 | GTCCATATTCAGATA[C/T]CTTTATTTGTCTCAA | 83860 |
rs560758165 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7969424 | AATACTGTCACATTT[A/G]GGATTAAGTACAATT | 83860 |
rs560772718 | snp | G/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816754 | ATGAACTTTCTGCAG[G/T]CTCATCTCTATTTCA | 83860 |
rs560776658 | snp | C/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014924 | TTGTTCACTCCCGAG[C/T]CGCCTTGGCCTGTGG | 83860 |
rs560780161 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916889 | TTTGAAGTAAGTTAA[C/T]TGACAAAAAGAAATG | 83860 |
rs560805552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7900836 | TTTGATTAGAAGCAC[A/G]TGGATTTTCTCCTAC | 83860 |
rs560806454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879260 | TTACTTTCACCAATT[A/G]TAGTTAAACTGTATG | 83860 |
rs560811588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961635 | CATCATGGTGACTTT[A/G]GTTATCTCAACAACA | 83860 |
rs560815255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8000735 | AGTGAGCCAAGATTG[C/T]ACCAGCACACTTTAG | 83860 |
rs560822900 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869859 | TGAATATATTTATGT[G/T]TATAAACTATTTGTA | 83860 |
rs560839839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852692 | TTGTGAATGTGTGGG[C/T]GTGATTTTAGCAAAC | 83860 |
rs560876133 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8000250 | GCCTCCTGAGTAGCT[A/G]GGATTACAGGCATGC | 83860 |
rs560882230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7864696 | TCTTTACCTATCCTG[A/G]TCATCAGTTTTTTAT | 83860 |
rs560898959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935729 | TCAGGGAGAGGCCCT[A/G]CAGGTCCACTGGGGA | 83860 |
rs560900318 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7906956 | TGATTCTTATCTAAG[A/T]CTTTGCATGTGAAGT | 83860 |
rs560927476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984296 | TTTACTAGAAAAAAA[C/T]AGTAAACTGTCAGAA | 83860 |
rs560928696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006856 | GGCAGTTCCCATCTG[A/G]ATGCAGTTTTTGAAG | 83860 |
rs560961671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900428 | TTGGAGATAAAATGG[A/G]TGACAGCTTTGTACA | 83860 |
rs560968426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949289 | AGCACAGCCGGAAAT[A/G]AAGAGTGGGCTGCTT | 83860 |
rs560970690 | in-del | -/AAT | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7983894 | AAGCAAAATAACAAC[-/AAT]GACAAAAAGAATTTT | 83860 |
rs560982193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819367 | AGCTCTGCTCCGTTA[A/G]GGACACTGCCTCGTC | 83860 |
rs560985471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7844891 | TTAGTTACTTAGCCA[A/G]TCGCTTATTGTTGGG | 83860 |
rs560992007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945566 | TGCCGCAGGGAGGCC[A/G]GGCCTGCCCTCGCAC | 83860 |
rs560992287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013909 | GAGATGAAGCATCCA[C/T]TGAGTAGATTCCTGC | 83860 |
rs560996003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852107 | ACCATCTCCCAGAGA[C/T]GGGGTCTCACTTTGT | 83860 |
rs561025329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906431 | GAAAAACCTGCTGCT[G/T]CATTGGGGAGGGGAA | 83860 |
rs561046129 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7908462 | TCATGTGAGCGGCTG[G/T]GAAGATTAAATGGGT | 83860 |
rs561078517 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7834144 | GTGTTTTCCTCCTCA[-/C]CCACAGGTTGTGCCT | 83860 |
rs561094297 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830081 | TGGCAGATGGGGCTC[A/C]TCTGCATCTTCCCGT | 83860 |
rs561101038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912909 | TTGTCGGTGTCTGCT[C/T]GGGCTGCCATCACAA | 83860 |
rs561123275 | in-del | -/AGTGCTG | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:8000378 | GTGTTGGCCTCCCAA[-/AGTGCTG]AGTGCTGGGATTACA | 83860 |
rs561124334 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842802 | TAATCAAATTAGATA[C/T]AAATGTCGTATATTT | 83860 |
rs561132442 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873229 | TAGTATTTTCTTCAA[C/G/T]ATTTTTTTTTTCTAA | 83860 |
rs561137328 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941583 | CACTGCCCTCTGCTT[C/T]GCCACTGCCTCACTG | 83860 |
rs561138711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978001 | CAGTACTCTTACCTG[A/C]TCCTAATAAGATAAT | 83860 |
rs561146365 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817935 | AGTCAGGAGTTTATG[C/G]CATGGATTTGGATTT | 83860 |
rs561159149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826495 | CTGGCTGAAATTACT[A/G]TATTACTATAGATTT | 83860 |
rs561166802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913596 | CTGTATAAACTTGTG[C/T]TCTCCAGCTTGTTGG | 83860 |
rs561170288 | snp | C/G | 3.402e-05 | 0.00412418 | intron-variant | TAF3 | GRCh38.p7 | 10:7824604 | AGTGATTATTTTAAT[C/G]GATTTTTAATCCTCT | 83860 |
rs561200389 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938080 | GTATGAATGTCTTTA[C/T]TAATAAAACATTTTT | 83860 |
rs561208730 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858657 | TACTGTTAATGAGAA[C/T]TTATTTTAGGATTGC | 83860 |
rs561236477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7833738 | ATTCTTCTCCTCAGT[A/G]GTGACTTGAGCTTTC | 83860 |
rs561241513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948948 | GGGAAAAAAGCAAGT[G/T]TAGGAACAGCTTCCT | 83860 |
rs561260784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865428 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCTCTGC | 83860 |
rs561264474 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015901 | ATACTGTAGCATTTT[A/G]TCTTTATATTGTTTT | 83860 |
rs561289844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957273 | TTTCATGGAGCGATG[A/G]GGAGATTAGGGCAGA | 83860 |
rs561308521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7826022 | ATCGGTTCTACTTTA[A/G]TAGCATTTTGAAGTG | 83860 |
rs561336383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865695 | TAGGCTTTCACAGGC[A/G]GGGGTGAAGGAAAAA | 83860 |
rs561342320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888348 | GATTCATTGAGACAG[C/T]GGAGAAAGTGTTTAA | 83860 |
rs561348686 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861282 | CGGCTAATTTTTGTA[-/T]TTTTTAGTAGAGATG | 83860 |
rs561378059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7822436 | AGAAGAAGAGTATTC[A/G]TTTTATTTATTTTCT | 83860 |
rs561384028 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7918049 | TTGTTTTTAGGATTC[A/G]GATATTATGGCATAT | 83860 |
rs561401238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860570 | AGAGGTGTAGTTCAT[A/G]TAGAAAAAAACAAAA | 83860 |
rs561443078 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858045 | ACAAAGAGGTTTGAA[C/T]GGCCTCAGTAGAATA | 83860 |
rs561512642 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7940752 | TGAGCCCAGGAGTTT[-/G]GAGACCAGCCTGAGC | 83860 |
rs561561606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889887 | TTTCTAATGCCACAG[A/G]TCCTGTTCTCATTTG | 83860 |
rs561573252 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991214 | ATATACATACATACA[C/T]ATCCGTATGCATGTA | 83860 |
rs561597246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7880088 | CCCAAAAATATAACA[A/G]ATTAGCTGGCCTTGG | 83860 |
rs561620318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7965994 | CAGACTATAAACTCT[C/G]TATTAGCTATAGTGA | 83860 |
rs561628598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7911495 | TAAGAAATGGCTGGT[A/G]TACTTGGTATGATAG | 83860 |
rs561637590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833317 | ATCTAAATTCCCACC[A/G]ACAGTGTACAAGGAT | 83860 |
rs561641165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7938855 | TAAATCCTGAGGGAG[C/T]GGAGATTTCTGTTTG | 83860 |
rs561659765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925321 | CTCTGCCATAATGGC[C/T]CAGCCTTGACTTACC | 83860 |
rs561660342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907944 | GGACTGAATCTGGAG[C/T]GGCAGCAGCAGGAAT | 83860 |
rs561661370 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844803 | TGTTCTGCTTTTTTT[C/T]AACGTATCATTTGTT | 83860 |
rs561673673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7925956 | CAGTGGCTCATGCCT[A/G]TAATCCTAGCACTTT | 83860 |
rs561674878 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837670 | AAATAAAACAATTAG[C/T]CAAGAGTGGTGATGT | 83860 |
rs561674952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7868422 | TAGTGACCATCAGGA[G/T]TGGAGGCAGTGTGAC | 83860 |
rs561682221 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7988439 | TACTAAAAATACAGA[A/T]ATTACACCTGTTATC | 83860 |
rs561694924 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7953155 | CACCTAATCCTCAAC[A/G]TTCCATCACGTTGTT | 83860 |
rs561712140 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7933454 | ATTGGTGACACTTCA[C/G]TTGGGCTATTGGACA | 83860 |
rs561722886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942896 | CAAAAATCACATTTG[C/T]AGGTTGGATTTCAGC | 83860 |
rs561723056 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7940754 | GAGCCCAGGAGTTTG[A/G]GACCAGCCTGAGCAA | 83860 |
rs561751140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7959735 | CTCACATTCTTCCTT[C/T]ATTCAAAGGCCTATC | 83860 |
rs561755132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7830173 | TCTCAAGCTCCTGCC[A/G]TCCTTTTCTTGAAGC | 83860 |
rs561763892 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7918142 | GCTGACTTGGGAAGA[A/G]GTAGTTCTGGTTGTT | 83860 |
rs561787459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011415 | TCTGCCACCACAACT[G/T]GCTGTTTCTTGGCTG | 83860 |
rs561790515 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7837156 | TTGCTTGAAGTCAGG[A/T]GTTCAAGACCAGCCT | 83860 |
rs561796244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7843499 | TTTAAGTAACTTTTA[A/G]TCTTTTTTGAACCCT | 83860 |
rs561806544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7883381 | CAGAAATACCGTAGA[C/T]GGTGGTGTGTTCTTC | 83860 |
rs561810351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013415 | CATAGTTATAGTTTT[C/T]TTTTTTATGAAAGGG | 83860 |
rs561852182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946677 | GCAGTGAGCCATGAT[A/T]GTGCCACTGCACTCC | 83860 |
rs561884918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960988 | TGAAGGAAGCAATGA[A/G]AGGTTTTTAAGATGA | 83860 |
rs561910205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7841775 | TGGCTAGGTAATCAG[A/G]TATCTAAATATCCAG | 83860 |
rs561910999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8011938 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCAGCTG | 83860 |
rs561912182 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912102 | AGAATAGGAAACATA[A/T]TATCCTCATTATTTC | 83860 |
rs561951014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990480 | GGTCAGGGTAAATTT[C/T]GAATGACCGCTACAT | 83860 |
rs561951745 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817072 | TAAAATCCCCTCCCC[A/T]ATACACAGAAAGGCA | 83860 |
rs561956968 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939168 | TGTTTATTAGCAAAA[A/G]CATTTGAATTTTTAG | 83860 |
rs562016987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891517 | AAGTCCTATGGCATA[A/C]CACTTACAGCAAATT | 83860 |
rs562018558 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880335 | TTTGACAGATTTTTG[C/T]ACATCTGAAAACAAA | 83860 |
rs562022133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877868 | TACCGTTTATACACC[A/G]TGTGTGTTATTTTGA | 83860 |
rs562049798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830983 | GATTTAGGTTTGGCA[A/G]GATATCAGCTGATGA | 83860 |
rs562057573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941476 | TGAATGGCTGGGGCA[A/G]GTCAGAGAGTGAAGA | 83860 |
rs562060742 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840309 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTGTT | 83860 |
rs562080999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7892355 | AGCTTCATGGAATGT[A/G]TGTTCCTTTCTTCAA | 83860 |
rs562189040 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963697 | ATAGCGTTAGGAGAA[A/G]TACCTAATGTAAATG | 83860 |
rs562212698 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7953885 | TTAACACAGAGCTCT[C/T]CATAGTGAGATTCAG | 83860 |
rs562214490 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843832 | GAAAATATAATGGTT[A/G]AATACACTCTTGTTA | 83860 |
rs562221534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982199 | TGCTTTTTATTCATA[C/T]ATAACTTTTTTCCTA | 83860 |
rs562238222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005463 | AATTCATGCCATTCT[C/T]GTGCATCTTTACCTT | 83860 |
rs562239702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905475 | ACTTTTTTAGTTTGG[A/G]TAACGAGTTCAGATG | 83860 |
rs562241355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7912815 | AGAAACGCTGTTTGG[C/T]GAGGCACTGGTGCTT | 83860 |
rs562259750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934477 | TGAGACAGAGTCTTG[A/T]TCTGTCACCCAGGCT | 83860 |
rs562262542 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7863462 | CTGAAAATACAAAAT[A/T]AGCTGGGTGTGGTGG | 83860 |
rs562270950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7912074 | ATTGTAGTTTGGGAG[A/G]TATTTTTTATGTAGA | 83860 |
rs562290138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898328 | AAGGTGGGTGGATCA[A/C]CTGAGGTCAGGAGTT | 83860 |
rs562297316 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7927268 | TGTCCATGGTGGCCA[C/T]GTAATTGCCATTCTC | 83860 |
rs562351306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883889 | GCTACATCTAGTGAG[A/C]GCCTTCTTGCTGGCG | 83860 |
rs562394674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012827 | AGCATGTCTAGTCAG[A/T]GTGGTATTTGAAAGT | 83860 |
rs562428547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974021 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 83860 |
rs562429173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960602 | GGAGTGTGACCACAT[A/G]TTTGGGGATTGCAGA | 83860 |
rs562429854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850125 | TCTGGGCCAGGGTAA[A/T]TTGCATAGCCAATAG | 83860 |
rs562443125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7830785 | CACCCCGCCCAACCA[C/T]GTCATTTACCTTTTA | 83860 |
rs562458023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8012344 | ATGCCACTTAAATTC[C/T]CTTAGCTCCGGTTTC | 83860 |
rs562474963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7918779 | TGGGTAGAAGTGGAG[A/G]GAACAGTAAACCAGG | 83860 |
rs562490075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966519 | GCTTTGCTTTTCAGT[A/C]TGTGGTTTCTTGGAT | 83860 |
rs562490131 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848681 | AGTGTTTTCATTTTT[A/G]TTGAAGCTGGCTTTG | 83860 |
rs562497565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926807 | AAGATTAGTAAGCAA[C/T]AGTTTTTAAACTTTG | 83860 |
rs562499774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869799 | TTTTTGATCTTTGGC[A/G]GACTGGTGAAAAATA | 83860 |
rs562524273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934964 | GGGAAAAAACACATA[A/G]AACAATAAATATTAA | 83860 |
rs562525427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934262 | GTTAGTCTAAAATAA[A/C]ATCCCTAAGTGATAA | 83860 |
rs562527003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974823 | GCTCACACCCGTAAT[C/T]CCAGCACTTTGGGAG | 83860 |
rs562534258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999093 | CTCATTAAGCAGATG[A/G]AAGGAAGGTAGGCAG | 83860 |
rs562589777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7933834 | TTCTTTGGCTATTAT[A/G]ATATTGGAGAAGAAA | 83860 |
rs562589855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864164 | GACAAATGTGTAATG[A/G]CAAATACCTGCCATT | 83860 |
rs562589988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857379 | GAGCAGTTTCTTCCC[A/G]CTGCCCCCTTAAACA | 83860 |
rs562595671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005511 | GGAATCCTTAGTGTC[A/G]GGAGGGAGTTCTATT | 83860 |
rs562611665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876911 | CCAGACCTATCACTT[C/G]TACTTTGATTTGCTG | 83860 |
rs562631498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832494 | AATGTGTAGTAATTA[C/G]ATCAGACTAAATTGG | 83860 |
rs562652942 | snp | A/C | 0.00542205 | 0.0517844 | intron-variant | TAF3 | GRCh38.p7 | 10:8014596 | GAGAAGAATAGATGT[A/C]TGTATAAAAGTTGCT | 83860 |
rs562691630 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997341 | TTGATAATTTGGATT[A/C]CTGGTTTCATCGTGT | 83860 |
rs562696120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8006052 | AAAACAAACAAGGCC[A/G]GGCACCGTGGCTTAC | 83860 |
rs562707953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961511 | TGATCTCTTTGACAT[C/T]TGACCCTCCATGTAT | 83860 |
rs562723725 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7941970 | TCATCATTTTCTCCC[A/G]AAGTGTCAAATTTAC | 83860 |
rs562782666 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7830284 | AGAACTTTACCAGCT[A/G]TCTCAGAATAGCTTC | 83860 |
rs562798645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928166 | CTTTGACCTTCCGCA[A/G]TGAAAGGACAAGGAA | 83860 |
rs562799834 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934283 | TAAGTGATAAAAATG[C/T]ATTGTCAGAATTTAA | 83860 |
rs562836100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877562 | TAATGAGAATATGGC[A/C]TTTATTGTTAGAATT | 83860 |
rs562862452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935528 | GGCGGAGCTTGCAGT[A/G]AGCCGAGATCGCGCC | 83860 |
rs562874241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983287 | GAAGGGGAAGTGGTA[A/G]GTTCCAGAAGGAAAG | 83860 |
rs562874306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991948 | CTTATTACCTTTAAT[A/G]TTTTCAAATAACTTG | 83860 |
rs562882290 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7886189 | CTGCTTTGGCCTCCC[G/T]AAGTGCTGGGTTTAC | 83860 |
rs562899100 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7899206 | ACATCCTTGCCTGTG[C/T]GCAGTCTCCCTCGAT | 83860 |
rs562921459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850295 | CATTTTATACTGCGA[C/T]GGATAGGACAATTCA | 83860 |
rs562925308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937669 | GTTGTGCTCCATCCT[A/G]AAGGATGAGTAACAG | 83860 |
rs562925364 | snp | C/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820269 | TATATTATTTGTCAT[C/G]TTGTTTTGTAATCAC | 83860 |
rs562931180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7840432 | GCTGGGATTACAAGC[A/G]TGAGCCACCGCGCCC | 83860 |
rs562943321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879132 | ATGAAATGTTTAATA[C/T]GGCCATGTTTAGAGG | 83860 |
rs562958804 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7906623 | CAAAGGCTCCTTATA[A/C]TTTTTTTTTCTTTCC | 83860 |
rs562969336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853558 | ATTCTTCAACTGTTA[C/T]CTGATTCAGCAAAGA | 83860 |
rs562986294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944389 | TAATTTTCTAGTTAG[G/T]CAGTAAGACCATCAA | 83860 |
rs562992550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834471 | CAAGTACACAGTCTC[G/T]GTGCTAAGGGATACT | 83860 |
rs562992812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840950 | CACCTCCCAGGTTCA[A/G]GCTATTCTCCTGCCT | 83860 |
rs563002170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7990718 | AATTCAGAGATTCCC[C/T]ATCAGTTCAAAGGTC | 83860 |
rs563029988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999681 | AGGCTGGTCTCAAAC[G/T]CCTGACCTCAGGCAG | 83860 |
rs563047578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943612 | GAAGAATAAATACTT[A/G]TCATTTCCTCTGAGC | 83860 |
rs563082632 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825851 | TCAGGTGTTTTTTTT[G/T]GGGTCTGTACCTTGA | 83860 |
rs563084461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975543 | TCGGTGCTCTAGGGG[A/T]TGGTTTTAGGTTGGT | 83860 |
rs563091629 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968462 | TGGGCTTTGGAATCC[A/C]GCAGACCTGGAATAA | 83860 |
rs563116576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899656 | AACACAAAGGAAGAA[A/G]TCAGAGGAAAAGCTT | 83860 |
rs563127595 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944135 | TGTGTGTGTGTGTGT[-/GT]TGTGGGGGGGAGGGA | 83860 |
rs563155019 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011673 | TTGTAGGTGTTTAAT[C/T]AGAGGCAACATCACC | 83860 |
rs563179831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976356 | AGTTCAAGCGATTCT[A/C]CTGCCTCAGCCTCTT | 83860 |
rs563192214 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010832 | CAAGAATTGCTTGAA[C/T]GGGAGGCAGAGCTTG | 83860 |
rs563200359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7843566 | TAAATGTAGTTATTC[A/G]TATCTAGTTTTACCA | 83860 |
rs563239377 | in-del | -/GGCAGGAGGATGATTTGAT | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7832982 | GGAGGATGATTTGAG[-/GGCAGGAGGATGATTTGAT]GCCAGGAGTTCGAGA | 83860 |
rs563241004 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7950744 | CTGAGGTCGAGCAAG[G/T]CAGCACTCTGCCTTT | 83860 |
rs563264060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002319 | ACCTGTGCTTTATCC[C/T]GTCGCACATCGTAAA | 83860 |
rs563272860 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856677 | AAGGAACAAGGGCTC[A/C]TTCGAAAAATGGCTT | 83860 |
rs563274916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987003 | ACTGCTGACTGTGCC[A/G]TGTGTATTTCAGCAA | 83860 |
rs563280226 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854640 | TCAGTGAAGAGAACT[G/T]AAAAGAGCCCTCTAA | 83860 |
rs563280332 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900149 | AACTTAGAATAGTTA[C/T]ACCAGTACTTTTGCC | 83860 |
rs563282239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881648 | CCCCTTGAAATTTGA[C/T]AGAGTAACAATCATG | 83860 |
rs563286806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846002 | TCTCGCCTGTCACCC[A/G]GGCTGGAGTGCAGTG | 83860 |
rs563295954 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833697 | GCATTGGCACGGGCC[A/G]TGCAGCAACTAGCAA | 83860 |
rs563321774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856076 | GAAGCCACAGAAGCA[A/G]CATTCCAGGCCAAAA | 83860 |
rs563341678 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934069 | TAACACTCTCGATAG[C/T]GTAGAGATTGATACT | 83860 |
rs563341695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7882398 | CATCTACCTCATTTT[A/G]TAACAGAGGAAATAA | 83860 |
rs563361212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902461 | ATCTTTTCTTAGGAG[A/T]TGTTATTAAGAGTCC | 83860 |
rs563367706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7874672 | ATATTAAAAATATGG[A/T]CTCTAACAGATATGT | 83860 |
rs563391063 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7931547 | TTCTACACTTCTGAC[A/T]TAATGAAACTGTAAA | 83860 |
rs563399920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856515 | ATTTTAAAAGAGAAA[A/C]GATTTTTTAAAAATT | 83860 |
rs563417436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895739 | CCTCTATCTACAGTT[A/G]TAGAATTTTTGCTTT | 83860 |
rs563428584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890057 | TTTTGACTTCCAGAT[A/G]AAAATCAAACACTTG | 83860 |
rs563439870 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007168 | ATGATGGACAAAAAC[C/G]TTTGGCTTACTAATA | 83860 |
rs563440626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958582 | ACTACAAAGGAAACA[C/G]ATTGAAGATCAAGAT | 83860 |
rs563440868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7965821 | AAGCCCACAATTATA[G/T]CTGTATTCTGGGTGT | 83860 |
rs563455713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7820379 | AGGCACCTGAGAAAT[A/G]TTTGTTGAATAAATG | 83860 |
rs563459634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902036 | GCAGACACTAACTCC[A/G]CACCCCACGTTCGTC | 83860 |
rs563466529 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835574 | CCTGGCAGAGAGCAG[C/G]CAGGGTCAAGTCTGA | 83860 |
rs563466929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7861030 | GCAGTGGCGCCATCT[C/T]GGCTCACTGCAAGCT | 83860 |
rs563485488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7890639 | TTCTTGCATAAAACA[C/T]ATTCTAGCATATCAT | 83860 |
rs563493729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895126 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 83860 |
rs563505883 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956187 | GTTTGAAATTATTTC[A/G]AATTTAAAAATTAAA | 83860 |
rs563557357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7846110 | ACTACAGGCGCCCGC[C/T]ACCACGCCTAGCTAA | 83860 |
rs563574027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7847992 | CCAGGCTGATCGCAA[A/T]CTCCTGACCTCAGGT | 83860 |
rs563582566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010632 | GTAAAACCAGCTGGA[C/T]GCAGTGGCTTACGCC | 83860 |
rs563595327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861676 | CAGACGTCATTTGTC[C/T]TACTGTTCCATGGAT | 83860 |
rs563611404 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908682 | CCACAAAGCACATAA[A/T]GAGGCAGAAGCTGAT | 83860 |
rs563612249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7987439 | GTATTTCATTTTACT[A/G]TTGTATCATCATTTA | 83860 |
rs563616745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7930455 | ATTGATTTTTCTGCT[C/T]CTCTAACACAATCTT | 83860 |
rs563645377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7896294 | GGGGGAAAACGTAGA[C/T]CAAAACCAATTCTTG | 83860 |
rs563649097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7979111 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 83860 |
rs563710473 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905010 | AGAGGAAAAGTGAAA[C/T]GTTTCTTGTATCCGT | 83860 |
rs563757235 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:8003298 | TGTAATTTTTGTGTG[G/T]TTACCCTAGAAATTA | 83860 |
rs563775970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926922 | TTTTACTGTTTGGTT[C/T]AACGTGTGTATATAT | 83860 |
rs563780410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925277 | TTGGTGTGGACATGT[A/G]TGTGGACCCTCTGGC | 83860 |
rs563806877 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999873 | CAACTTAGACGCACT[A/C]GATTGTGCAGCTCCT | 83860 |
rs563815963 | in-del | -/T | 0.368529 | 0.220116 | intron-variant | TAF3 | GRCh38.p7 | 10:7873626 | AGTTCTCCCCCCCCC[-/T]CCCGTCAAAAGGGGG | 83860 |
rs563827821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829283 | ACCTTTTACGTGACT[A/G]TGGTACGTGTATCAC | 83860 |
rs563843122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916369 | CCATCACCCTGCTGT[A/G]ACTCATCAGCGTCAC | 83860 |
rs563853851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875697 | TGGTCCTTTTAAAAT[A/G]TATCTAGTTTAGTGA | 83860 |
rs563891262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903296 | TTGACAAATGAGAGG[A/C]CCCTACAGGTGACCC | 83860 |
rs563904976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917193 | AAACATTTGATAAAA[A/T]TTCAGGCGGTAATAA | 83860 |
rs563926937 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7885995 | GTGTAGTGGCGCGAC[G/T]ATGGCTCACTACAGC | 83860 |
rs563938652 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998042 | CATCACAAAAATAAC[C/T]TTAGCTTAAGTCAAA | 83860 |
rs563949144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946490 | GCACATTGGGAGGCC[A/G]AGGCAGGCAGATTAT | 83860 |
rs564012054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952914 | TTTTAAAATATTTTA[C/T]AAGGAGATGTCAATG | 83860 |
rs564023322 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837478 | CGAAACCTCGTCTCT[A/G]CTAAAAATACAAAAA | 83860 |
rs564030221 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7917351 | AGGTGAAAACATTTC[A/G]GGCACGAGGAACAGC | 83860 |
rs564038097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945302 | AATAACTGATTTCCT[A/G]TTGGGTGTGGTTGTT | 83860 |
rs564071636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841580 | ATTCTGTTGGTACTG[A/C]GAAGGATGGACTCAA | 83860 |
rs564072233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875511 | GGATGTGTGGAAACC[C/T]CCACTGAAAACGGAT | 83860 |
rs564076456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7988352 | CCTAACACTTTGGGA[A/G]GCCAAGGCAAACAGA | 83860 |
rs564082595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883194 | TAGGAGTCCCGTGGT[A/G]CATTCAGTCAGCCTT | 83860 |
rs564093132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938660 | CAAGCCAAGATGCCT[A/G]GTAGGAAATGAAAGC | 83860 |
rs564116898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7849459 | GGGACGATTTAGGGT[C/T]ATTGCATGGGATGTG | 83860 |
rs564126424 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951075 | GTATGCATCGATTAG[C/T]TGATGAAAATGTTGT | 83860 |
rs564136072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835367 | ATTCAGGGTAGCTCC[C/T]CTGACTTTGCAGTGC | 83860 |
rs564172298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953013 | GCCATGCCCTTCTTT[C/T]CCTTCCCAGCATCGA | 83860 |
rs564178301 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7850026 | GAATATTATTTGTTA[A/G]AAATTGTTGGGATTC | 83860 |
rs564185690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7959122 | CCTAGCCTGGGTGAC[A/G]GAACGAGATTCTGTC | 83860 |
rs564186390 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954527 | GTGCACTCCATAGGC[A/G]AATGAGTGAATTAGT | 83860 |
rs564201899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889021 | TTTTTTTTTCTACAC[A/G]TGGGATATTGGAGCT | 83860 |
rs564237729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952406 | TTGTCGTTATCATAA[A/G]TCATATCATAAATAA | 83860 |
rs564237786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960332 | AGGGAAAAGTTTAGA[C/T]GAGCTGAATGTGGTA | 83860 |
rs564249821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855288 | TCCTCCCTGGTTTGG[C/T]GCAGCTGAGCAGCTG | 83860 |
rs564263175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966420 | ACTTCATTTCATAGC[A/G]TACAGCCCGACAAAC | 83860 |
rs564296251 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TAF3 | GRCh38.p7 | 10:7946536 | TGAGACCAGCCTGGG[C/T]GACGTGGCCAAACCT | 83860 |
rs564311134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7847263 | GTCAATATGAATTGA[C/T]ATATGTCTAAGAACA | 83860 |
rs564336987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890794 | TCACACCTACGTCAT[A/G]CATTTTTTTCCCAAG | 83860 |
rs564345286 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967911 | TATTAGCCCTTGATA[C/T]AAATAGGAAAGGATA | 83860 |
rs564383059 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979083 | GATGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 83860 |
rs564402832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884140 | CTGGGGACTGGGTTT[C/T]GACATGAGTTTTGGA | 83860 |
rs564415939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980615 | AAACCAAAACCTAAC[C/T]CTGAAATTACAGTCT | 83860 |
rs564423372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981594 | ACTCCTTTTTCAAAA[C/T]ATACAAATTATGTCA | 83860 |
rs564428604 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7956271 | GAGGTGGGCAGATCA[C/T]GAGGTCAGGAGTTTG | 83860 |
rs564452772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889702 | TAATTATTTCTTCCA[C/T]TGGCCTGGTCCTGTC | 83860 |
rs564454375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856551 | ACCAGTCCAGGAAGC[C/T]TAATATCTGAACAAC | 83860 |
rs564482494 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881870 | AAAGAAAAGGATAAC[G/T]GATTTTTGTGATTCT | 83860 |
rs564488900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898937 | TACTGTCAGGGATGG[C/T]AAGTGGTGCGTTGAA | 83860 |
rs564490412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910626 | CCTCAAATGATCCAC[C/G]CACCTCGGCCTCCCA | 83860 |
rs564510996 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7862593 | ATATGTATATACTTG[G/T]GAAAGCATTGTCACA | 83860 |
rs564518569 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7852840 | GTGGTAGAGTTTGTA[C/T]ATGAAAAGCTGGATG | 83860 |
rs564564272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947995 | ATAACTTCCTGACAT[A/G]CCTTTTATTAAAGAA | 83860 |
rs564575730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7956056 | AAGTTTCCCAAAATT[A/G]TACTATAATTAGGTA | 83860 |
rs564602223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004169 | GATTCTCCTGCCTCC[C/T]CCTCTGGAGTAGCTG | 83860 |
rs564605968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011349 | GCCTCGACCTCCTGG[A/G]CCCCAGTGATCCCCT | 83860 |
rs564609636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842901 | CACTGAATGTAATGG[C/T]TGTCATACTTTGTTT | 83860 |
rs564622930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887017 | GAGGCAGGCGGATCA[C/T]GAGGTCAGGAGCCTG | 83860 |
rs564625678 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976446 | TTGAGACGGAGTCTC[A/G]CTGTGTTGCCCAGGC | 83860 |
rs564632950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955020 | TGAATGAATTAGTCC[C/T]AGTTAACACAGAGCT | 83860 |
rs564633737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7939897 | ATGAAACTAAAGGAA[A/G]TGAAATTATCAAAGA | 83860 |
rs564643692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7884674 | ATTACAGGCGTGCGC[C/T]GCTGCGCCTGGCCTG | 83860 |
rs564654541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934327 | TTTCGTTAATGGCAC[A/G]TAAAATAAGTGTGTC | 83860 |
rs564719655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7933890 | ACGTTTTCCCCCCGA[G/T]TTTAGCATTTCTGAA | 83860 |
rs564735112 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829823 | TGGGAGTTATGCGTC[C/G]CGCTTTGAAGGTGGA | 83860 |
rs564743183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986149 | TTTTTTTTCCCCCTT[C/G]TTTTCTTTTTGCCCT | 83860 |
rs564749323 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894518 | AGATGGTGACTGGAC[C/G]TAGGTGGTTGAACTG | 83860 |
rs564752855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862931 | ACAATTTCTTTACCC[A/G]TTCAGCTGTTAATTG | 83860 |
rs564753470 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828069 | TAGTGAAGTCACGCT[A/G]TAAGGGGAATCGGTG | 83860 |
rs564772145 | in-del | -/TATATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998242 | AATCTGAGTGAGAAC[-/TATATA]TATATATATATATAT | 83860 |
rs564774150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825804 | TGCCGCTATGAACAT[C/T]GATGTGCAAATCTCT | 83860 |
rs564790280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858873 | GTGAGTGTGCGTGTG[G/T]GCATATGAACATGTG | 83860 |
rs564813600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895018 | GAAGCTGGGATTACA[A/G]GTGCCCACCACCATT | 83860 |
rs564846466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998789 | GGTTGCAGTGAGCCG[A/G]GATCGCGCCACTGCA | 83860 |
rs564853519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859784 | GTCAATTTTATTCAC[C/T]GTTTCATTCCTAGCA | 83860 |
rs564889087 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872540 | TGAGCAAATTACTCA[A/G]TGGGGAACGTTTAAA | 83860 |
rs564893786 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7901798 | TGACTAAGGCTGTGA[C/T]GGTCACATTTAAATA | 83860 |
rs564900261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7921239 | GTAGAAGGAAAGAGC[A/G]GTTTTATTTGGTAGT | 83860 |
rs564903150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7897830 | ATGCCCGGCTAACTT[C/T]TTGATTTATTTGTAG | 83860 |
rs564917201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894222 | ATTTTTTCCACTTCT[C/T]CTACCCCTAAGCAAT | 83860 |
rs564937640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845537 | AAGGGTATGTGGAAG[C/T]GAGAATGTGTTTGAG | 83860 |
rs564966001 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7914183 | TGATGGCGATGTGGT[A/T]ATACATATTCTTAAA | 83860 |
rs564994344 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003356 | ACAGTTTATATAATA[C/G]AGGGACATTAAAATA | 83860 |
rs565000023 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016167 | AAATACGGACTTTTA[C/T]TTGATTTTGAAATAA | 83860 |
rs565001038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994118 | TTTCTCTTTCTCTTT[G/T]GTTTTCATGTTCATA | 83860 |
rs565006759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8007009 | ACAGTCCACAGGCTG[G/T]CAATTCCTGGTGAGG | 83860 |
rs565030506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7909664 | GCAAAAGGAAACTAT[A/G]GTGCTTAACAGTCTA | 83860 |
rs565039983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949963 | GGCCCAATTTCAGAG[A/G]TGCACATTTTTGTTT | 83860 |
rs565057913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936843 | CTTCTCTTCATCCCT[C/T]CCTCCCTGTACCCGC | 83860 |
rs565080612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864815 | GTTTTAAGGAAATAT[A/G]GTTTATCTTTTTTTT | 83860 |
rs565102697 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TAF3 | GRCh38.p7 | 10:7915426 | GAGACGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 83860 |
rs565121585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936150 | GGACAACAAGGAAGA[C/T]GGGCCCTGAAGACAG | 83860 |
rs565123650 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002538 | TTGTTCCTTTGAGGA[A/G]CTACTGATAGAGCAG | 83860 |
rs565148706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880820 | TCTTGATGATGCGTG[C/G]AACAGATGTATATTT | 83860 |
rs565175023 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7907762 | ATGAAAGCTGCTATT[A/T]TAATAATGTGGAGCC | 83860 |
rs565186642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861165 | GAGATTGGGTTTCAC[G/T]GTGTTAGCCAGGGTG | 83860 |
rs565192221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942890 | CATACACAAAAATCA[A/C]ATTTGCAGGTTGGAT | 83860 |
rs565211220 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8009907 | TTACAGGCATGAGCC[A/C]CCGTGCCCGGCTTTT | 83860 |
rs565211512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873297 | GAAATTGTGTTTCTC[C/T]CTAACAGACCTATTT | 83860 |
rs565220776 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926261 | CATATTTTAATATAT[C/G]AAACTTTTTTTTTAT | 83860 |
rs565229434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827553 | TTGGGAGGCGGAGAC[A/G]GGCGGATCACGAGGT | 83860 |
rs565236235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820011 | AGCAGTACACAGTTC[C/T]CTTTGTGAGCTAGCA | 83860 |
rs565289383 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845310 | CCTCCAGGTCTTTGT[A/G]TGTGTGCGTGTGTGT | 83860 |
rs565303352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963561 | TTTTTTTTAGAAATC[A/G]TGTTTGAACGCCGCA | 83860 |
rs565391788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7854428 | ACACATGGAAGCTCT[A/G]TGTGATTTTTGGCTC | 83860 |
rs565393293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861567 | AGTCCATAAAAAATG[A/G]TTATATAATTCTGTA | 83860 |
rs565399838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929654 | CACGTGTGAGCCACC[A/G]TGCCTGGCCCTATAT | 83860 |
rs565416032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7872644 | AATAATAATACAGGA[C/T]AACTAATTCTTGCAG | 83860 |
rs565452030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944457 | TAAGAGAAAGAAATA[A/C]AAAATGAAACGCAGT | 83860 |
rs565453569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951449 | ACACTTCATCACCCC[A/G]CAGGCTAACCTGGGC | 83860 |
rs565461626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7947933 | TCTAACTGAAATCAC[C/T]CATGTACAGACAGGA | 83860 |
rs565464549 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7934513 | GCAGTGGCACGATCT[A/C]AGCTCATTGCAACCT | 83860 |
rs565495262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887128 | TAGTCCCAGCTACTC[A/G]GGAGACAGGCAGAGA | 83860 |
rs565503871 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7833812 | GCTGGGTGGCCAATT[G/T]CAGTTCTTCAGCAGA | 83860 |
rs565505060 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971150 | CTGTCTCAGCTGTCT[A/G]CATGGGGTGGCACTT | 83860 |
rs565515324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936315 | GGCATTGTGGGGTCT[C/G]TCAAAAGCTATAAAA | 83860 |
rs565523527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839173 | CAAAAATAACTATGT[A/G]CCTGGGTCAGCTCAT | 83860 |
rs565542541 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849210 | ATGAGGGAAATAAAG[C/T]GTAGGGATAACTTTT | 83860 |
rs565550646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7985432 | AGCCTTTCATTCTCC[C/T]ATGCTAACCCTCCTC | 83860 |
rs565568474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826744 | GTAAGATGCTTGTCA[A/G]AACGTTCTCCTCTTC | 83860 |
rs565579435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942932 | GCTGTCTGTGCAGGT[A/C]TTCTGCTCTTAACAG | 83860 |
rs565585723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833447 | TTTCTGTAATGATTA[A/G]TAATGTTGAACATTT | 83860 |
rs565591917 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996629 | GTCTTTTTTTTTTGT[A/G]TTTGTTGTGAGGGGG | 83860 |
rs565598179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865730 | AAGTTGCTTAGTAAA[A/T]GTGCTTCTCTTGAAT | 83860 |
rs565626369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879597 | ACAAAGTGTAAACAC[C/T]GGCTCTTTTTGTAAG | 83860 |
rs565656860 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7928594 | GCCAGTGAAGCTTGT[A/G]GGATTGCCCTTGTGT | 83860 |
rs565661375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845633 | ATATCTGTGAGTATT[A/G]TAGCAGTATCTGATC | 83860 |
rs565696790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895509 | ATCATGGTCCTGGCA[C/T]GAACACCTTGGCCTG | 83860 |
rs565709559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7935828 | GAAAAGTGCAACTGG[A/C]CCTGAACGAGGGAGA | 83860 |
rs565728917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922203 | CTTCTGTCTACTTGA[A/G]TTTGTTTTTGCTCAT | 83860 |
rs565733864 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866080 | TGGATAAAGGAAACA[C/G]TTAATAGCAGTTTTT | 83860 |
rs565754717 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827678 | CCAGCTACTCGGGAG[G/T]CTGAGGCAGGAGAAT | 83860 |
rs565756799 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998941 | TATGTGTTTGGTATA[A/G]CTGAAAACAATGTAA | 83860 |
rs565780156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914426 | GCACTTATAATCTGT[C/T]GGTAAGAGTATTTTG | 83860 |
rs565787365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826142 | CAGCTACTGGACCTA[A/C]GTGGTAGGGATTTGT | 83860 |
rs565788709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8001852 | GTAATTATTGCATAG[C/T]AAAGCACATGAACAT | 83860 |
rs565793217 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7922746 | TTTACATACTGGAAC[A/G]TATAAAAGGTATTCT | 83860 |
rs565804686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992488 | ATCTAAAATTATAAA[G/T]AAGTTCAAGGTGATT | 83860 |
rs565838034 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994011 | CTCTCTCTGTCTCTT[C/T]TTCTCCCCCATCCCT | 83860 |
rs565897918 | in-del | -/T | 0.316968 | 0.240864 | intron-variant | TAF3 | GRCh38.p7 | 10:7840157 | TTAGGAAAATGAGTG[-/T]TTTTTTTTTTTTCGA | 83860 |
rs565937946 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888185 | TGTCTTCCTCTAGGC[C/G]AGGATCTACACCCCT | 83860 |
rs565942617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7865850 | CTTCCTTTCTGCTCC[C/T]TCTAGCTGCTCCGTT | 83860 |
rs565972424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894280 | TCAGCAGGGACAGTC[A/G]GCCCTCAGGGAACAT | 83860 |
rs565984690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7838786 | TCCTAGTTAAGGATC[C/T]GGCTGCCTCTCTCTT | 83860 |
rs565989249 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | TAF3 | GRCh38.p7 | 10:8003199 | TTTAGTGTTCAGTGG[-/T]TTTTTTTTCTCTCTC | 83860 |
rs565994141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929176 | AGGTCTTCAACTATA[C/T]TGTACTATAGTTATA | 83860 |
rs566007853 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838437 | CCCAGGCCAGAGTGC[A/G]GTGGCCTGATCTCGA | 83860 |
rs566042280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7951004 | GAGTTCAATGTTAAT[A/G]CATCATTAATATCTT | 83860 |
rs566042964 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7965981 | AGGCATCTAATCACA[C/G]ACTATAAACTCTCTA | 83860 |
rs566054105 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TAF3 | GRCh38.p7 | 10:7994824 | CAAAAAAAAAAAAAA[A/C]AATAGCTGGGTGTGG | 83860 |
rs566056918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008722 | CCTGTCAGGCCCCCC[C/G]GAGGACTCAGCAGAG | 83860 |
rs566073114 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7846153 | TGGTAGAGATGGGGT[G/T]TCACCGTGTTAGCCA | 83860 |
rs566090993 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943847 | CCATCTATTACCACA[A/G]ATAGTCAGGAACTGA | 83860 |
rs566094592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898654 | AAGATGTCTGAAGCT[C/G]TTCAAGCACTGGGTT | 83860 |
rs566101067 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7864928 | TCTTCTAGAAGTTTT[A/G]TAGTTTTAGGTTTTG | 83860 |
rs566109855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950355 | CTGTGGAGGGAAAGA[C/T]CTTGGCACCTTCCAG | 83860 |
rs566111010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947868 | CTCATCCATCACATG[A/G]CTTTATGTGAAGAAG | 83860 |
rs566114445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915059 | CATTCTTCTGCCTCA[C/G]CCTCCTGAGTAGCTG | 83860 |
rs566119166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7930937 | TTTATAAGTCCCACA[A/G]GTTTGTCTTTCCAGA | 83860 |
rs566140541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840031 | AAAAACAGAAGCACA[C/T]TTCCAATGCTATAGT | 83860 |
rs566152294 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967783 | AACTATAAAATGTAG[C/G]AACCTGGAGATTGCT | 83860 |
rs566157102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899319 | AGGAATCGCTGCCTG[A/G]CTACTTGAGGTTGTG | 83860 |
rs566178015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908705 | AAGCTGATCTCAAAC[A/G]TTTTTCAAGCCACAA | 83860 |
rs566182107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937836 | AAGGGGTACTTTTTT[A/T]ATGCTCTTTTGTAGA | 83860 |
rs566192088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004976 | AATTTATTTTGTCCT[A/T]ATACTCAGTTTATAG | 83860 |
rs566197520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840650 | AAGACGGGAATATCA[A/G]GGAGGAGCAGGCAAT | 83860 |
rs566207909 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823238 | GCCAGCTATGTGCCA[C/G]CCACTGTTTAAGATT | 83860 |
rs566217027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7987193 | CAGGTATGGTGGCAT[A/G]TGCCTTTAGTCCCAC | 83860 |
rs566249684 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870458 | ATATAATTTATTTAC[A/G]TGAGTGTTGCCTGAT | 83860 |
rs566275920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853746 | TGGCACTACAATGGC[A/G]GAGATGAGATGTGAC | 83860 |
rs566292899 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991809 | TTGAATTTTAATATA[C/T]TTTGAAGTGGTAATG | 83860 |
rs566338317 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919235 | GTAAAATGTGATTAT[C/T]GGTCTTGATTATCTC | 83860 |
rs566338351 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893525 | CATTCATATCCTCAG[C/G]TATTTTTCTCTCTGT | 83860 |
rs566341151 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7869253 | ACTTCTACCGTGTGT[C/G]TGTGTGTCTGTGTGT | 83860 |
rs566344060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998458 | ACCCATAAAATTGGT[C/T]AACAATCTGTTTCTA | 83860 |
rs566367941 | in-del | -/AAATAAA | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7944452 | TTTATTAAGAGAAAG[-/AAATAAA]AAATGAAACGCAGTA | 83860 |
rs566374609 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7891087 | GCAGATGTGTTTTAG[A/G]GAAAAATGGAGAGGA | 83860 |
rs566399593 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917639 | CTCTCTGGAGAATAG[G/T]TCGGGTTCTGAGGCC | 83860 |
rs566450460 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008092 | CCGTCTGGGAACAAT[-/C]TTTTTTTTTTTTTTT | 83860 |
rs566467815 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8017118 | AAGGAAGTTCAAGAA[A/G]CTGCAAAGAGAAATG | 83860 |
rs566472720 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TAF3 | GRCh38.p7 | 10:7849881 | TACCAGGTTTTCACC[A/G]TGTTGCCCAGGCTGG | 83860 |
rs566521738 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7838222 | GAGTCGGATCCTACA[C/G]AAGGAACTGGTGTTG | 83860 |
rs566527634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7911077 | TTTGACTTTAATTAT[A/G]TGATTTTTGAGGGAG | 83860 |
rs566553734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960651 | ATGGGTAGAGCACGC[A/T]GGGGCTCACTGTGAA | 83860 |
rs566557994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862797 | GTACTGTTTTTTGGT[C/T]TGGCCTTTTTTCACC | 83860 |
rs566571081 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818122 | AAGCAGCTCAATACA[A/C]AGATTTTTAGCTGAG | 83860 |
rs566593242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7843034 | GCGTAGTCTGTGTCT[C/G]TCTGGGGCTTTTACT | 83860 |
rs566619643 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818608 | GGGGACCCTTTCCCC[G/T]CCGCGGAAGCCCTAG | 83860 |
rs566635673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934575 | TCAGCCTCCCAAGTA[G/T]CTGGGATTACAAGCA | 83860 |
rs566638431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7830334 | CACCCCTTCCTCCCT[C/T]CCTCCAAAAATAACC | 83860 |
rs566657435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7940255 | AGACATGTGGAGTCT[C/G]AAAACATTTACTTCC | 83860 |
rs566662775 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821990 | CTAGTTCATTCCAAG[A/G]GTGTCTGAGTAAAAT | 83860 |
rs566686793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949742 | AGACTGTGAAGCAAT[G/T]CTTTCTTCTATAAAA | 83860 |
rs566687375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949079 | AGGATGATTTCCCAT[C/T]ACTTTTTTATCGACT | 83860 |
rs566698424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941056 | TGCAGTGCTGCTGGA[A/G]GGAAGAAAAGTCAAG | 83860 |
rs566701662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823227 | ATTTATTGAGTGCCA[A/G]CTATGTGCCAGCCAC | 83860 |
rs566710908 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7979914 | CCTGAAAGTTAAGAA[A/T]GTGTTTTATATTTCT | 83860 |
rs566711395 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7928306 | GCCACATAGGAAGTA[C/G]TTAAGTATTTTTTGA | 83860 |
rs566725288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865404 | GAATGGTGTGAACCC[A/G]GGAGGCGGAGCTTGC | 83860 |
rs566731905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7990801 | GAGCACAGGAGGTGC[A/G]TTAGAGAGTCCTGCT | 83860 |
rs566733716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7863211 | TAAAATTTCAAATCA[A/G]TGTATCATCTACAAG | 83860 |
rs566760525 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935453 | GCCTGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 83860 |
rs566772720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919102 | TGCATTTCAGAGGGT[A/T]CAGAATCTGAAAAAA | 83860 |
rs566775192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947581 | GAGAGCCAAATAATA[C/T]GAGAGAAGCAGCCGT | 83860 |
rs566794188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999210 | AGTAGTAGGTATTCT[A/G]TTTAAAGCTGATTAA | 83860 |
rs566816872 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TAF3 | GRCh38.p7 | 10:7858834 | TGTGTGTGTGCGCGC[A/G]CCTGCATGTCACTGA | 83860 |
rs566829143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967465 | TGGTGGAAGGCAAAG[A/G]CTCAGTCCCTCGAAG | 83860 |
rs566829978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824104 | TTTTCTGTGGTGTTC[C/T]GGCTAGTTGTCTGAT | 83860 |
rs566836132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919537 | GAGCACCAGTGGGAA[C/T]GGGGTTATAGTACGG | 83860 |
rs566836566 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011451 | GTTTGTTTGTTTTTG[G/T]TTTTTGTGGAGATGA | 83860 |
rs566842821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013645 | TTTATTCGGTTAACA[A/G]TATAAAGTAATCATT | 83860 |
rs566855139 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7907084 | TAGCTTTCTGTAGGA[C/T]TGAATAACTTACAGC | 83860 |
rs566868215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864440 | TCTTTGTGGTAAGGG[C/T]ACTTAACATCCACTC | 83860 |
rs566876065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968281 | CCTTCTCATCATCCT[A/G]ACCAAGAGCAACTCT | 83860 |
rs566879063 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882860 | CCTAAGTATTCTTTA[C/T]GTAGATTCCCCAAAT | 83860 |
rs566879650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891957 | TATTACAATATGTAT[A/G]TAAATTGTAACAGTG | 83860 |
rs566887066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7859044 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 83860 |
rs566896966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906605 | GAACAAATGTGACAC[G/T]GACAAAGGCTCCTTA | 83860 |
rs566904980 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7867270 | ACACACACACACACA[A/C]AAAAAACAAAAAACA | 83860 |
rs566911410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7999759 | ACCGTGCCCAGCCCA[A/G]ATGTATTACTTTATG | 83860 |
rs566943586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7892722 | TCAGCCAGTTAGTTG[A/G]TCAGTTAGTCTATCT | 83860 |
rs566944323 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846598 | TTTCATGATTTTTAT[A/T]CTTTCCTAGAGGCTA | 83860 |
rs566948524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8008919 | GTAAGTGGAGAGGCC[A/G]CTTCATGCAGGGCCT | 83860 |
rs566968324 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865634 | GCAGCCCCGGCAGGG[C/T]GGATGCAGCCACGTG | 83860 |
rs566968393 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892434 | TTGATTACAAAATTT[G/T]GTAAACATAGTCAAA | 83860 |
rs566973075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900000 | GTGGACATGTTAGGC[A/G]GCGTCCACTCATATC | 83860 |
rs566974199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8000708 | CAAATAAGCCTGGGA[A/G]GCAGAGGTTGCAGTG | 83860 |
rs567003963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7885989 | GCTGGTGTGTAGTGG[C/T]GCGACGATGGCTCAC | 83860 |
rs567011662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7975214 | AATTGTGGGCACAGA[A/G]AAGTTTGTAGGGAAT | 83860 |
rs567017668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983404 | CATTTTTATAAAAGT[G/T]TCCTGGGGAGGCAGG | 83860 |
rs567037751 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7837468 | GCCAGCATGGCGAAA[C/T]CTCGTCTCTACTAAA | 83860 |
rs567071719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014210 | GTGGTACAAACTGCA[A/G]GACTAAAGACTGCTT | 83860 |
rs567086844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878016 | CTTGGCATTTATTCA[A/G]TAAACATTTTTTTTA | 83860 |
rs567111237 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959384 | AAGTGATTTAGTTTT[A/G]TAATTCATTTCTATT | 83860 |
rs567113767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899790 | TGTGCTCTATAGTAT[C/G]TTGTAAAAATAAACA | 83860 |
rs567130721 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TAF3 | GRCh38.p7 | 10:7863732 | ATACACATATATATA[C/T]ACACATATATATATA | 83860 |
rs567132523 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843204 | CCTCAAATTCCCAGA[C/G]TCAAGCAATCCTCCC | 83860 |
rs567142556 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891912 | AGTATCTACTTTGCT[A/T]GTTAACTCAAGTACA | 83860 |
rs567148273 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7870177 | ATAGAGGTTTAACTT[G/T]GAACTCATTCTTATG | 83860 |
rs567175801 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000640 | AAAAATTAGCCAGGC[A/G]TGGTGGCACGCACCT | 83860 |
rs567193950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8006500 | TCAATAAATATTCAT[C/T]GGTTATGATGTTAAG | 83860 |
rs567237286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941103 | GTTAGGTTGGAAACA[G/T]AGAGAGCCACAAATA | 83860 |
rs567238908 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7948207 | AGCTGGGTCCACAGG[G/T]GGGCACCACTGGGCC | 83860 |
rs567242279 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000422 | CACCCGGCCTTTTTC[-/T]TTTTTTTTATGCAAG | 83860 |
rs567250919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991335 | AATTCTAAAGCAACT[A/C]AAATGATTATTCATT | 83860 |
rs567282745 | in-del | -/AAAAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925809 | ATCTCAAAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAG | 83860 |
rs567295716 | snp | C/T | 1.8529e-05 | 0.00304371 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818763 | GGTGGCGCAGATCTG[C/T]CAGGCGCTGGGCTGG | 83860 |
rs567319162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7905192 | ATGAAATACACCCTA[C/T]GTTAGAGTTTGAGAC | 83860 |
rs567328412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7844066 | CTTGTTTTAGAAAGG[A/C]TAGTAACAATTTGTT | 83860 |
rs567422447 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816884 | TGGGGTTAAGTGTCA[A/T]GAAGTTTGCAGCTTA | 83860 |
rs567441123 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7912465 | TAATAATTTAGGATA[C/T]TTTTTTTTTTCTGGG | 83860 |
rs567464518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975998 | ATCCTACAGCCCCAC[C/T]GAAAGACTTGGAGAT | 83860 |
rs567477066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982923 | AGCTCTTAAGCACCT[A/C]TTCATCTCTAGTGGA | 83860 |
rs567489155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7905663 | GAGGCGGGCAGATTA[C/T]GAGGTCAGGAGTTCG | 83860 |
rs567516194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983434 | GGCAAAGAACCTGGT[C/T]GGTGTACAAAAGGAT | 83860 |
rs567522040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857467 | AGTAGCCATGGGTAC[C/T]CCCAGAGAGGAAGGG | 83860 |
rs567526410 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845744 | CATTTTCAATTGGCC[G/T]TGTGAGAGGCCATTC | 83860 |
rs567550924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899400 | GTCCATCTTCCCAGG[G/T]ACCTGGCGCCTCTGA | 83860 |
rs567553475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942476 | TGACGTTGCTTTATG[C/T]GAGTAACAGCAGTGT | 83860 |
rs567564605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913285 | GGACATGATTGAGTT[C/T]ATAGCAGATGGCAGT | 83860 |
rs567610621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7955416 | AGAAGTCTAGCTTTA[A/G]ATACGTTTAATTTTT | 83860 |
rs567620335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7907226 | GTTGCATCAGAGCTT[C/T]GCAACACCCTCGGAA | 83860 |
rs567632309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8007222 | AGAATAAATAATATA[A/G]ATCTCTATGTGTCAG | 83860 |
rs567648380 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7901388 | TTATAAAAACAAAGA[A/C]ATTAATTATCCAGTA | 83860 |
rs567657994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7859123 | AAAAATTAGCTGGGC[A/G]TGTGGTGGGCACCTG | 83860 |
rs567659109 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840964 | AAGCTATTCTCCTGC[C/T]TCAGCCTCCCAAGTA | 83860 |
rs567670879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7853032 | CCATTGATGTTCAAA[C/T]TGTCCCATCTTTGGC | 83860 |
rs567684176 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7900628 | AAAAGGTAGAAAGTT[A/G]TGAAATGATTCAGAT | 83860 |
rs567690443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014330 | TCAGATACAAAAAAG[A/G]TAGCAACCTGTTCAG | 83860 |
rs567727651 | snp | A/C | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016238 | AATATGGGCTTTGAA[A/C]CTAATACAAATATAT | 83860 |
rs567742655 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985933 | GGACTATGGGCACCC[A/G]CCCCCACACCCAGCT | 83860 |
rs567750465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968823 | ATTATGTTAAAATGG[C/G]ATAAGTGAAATCACT | 83860 |
rs567760917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893713 | GCCTATCTGTGTATG[C/T]TCACCAAGGTTCCCT | 83860 |
rs567765219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845289 | CTGTTATTTTTTTGA[C/T]GCCGCCCTCCAGGTC | 83860 |
rs567818442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7902311 | GTCTGTAATCCCAAC[C/T]ACTCGGGAGGCTGAG | 83860 |
rs567819685 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981953 | TAAACTTTTCCAGTT[A/G]ATGCTTTTTGACAAT | 83860 |
rs567832873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871746 | ACCGCGCCAGGCCAA[C/T]GATTGCTATTTTGAC | 83860 |
rs567848221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7847731 | ATTACAGATGTGAGC[C/T]ACCATGCCTGGTATG | 83860 |
rs567851743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7993439 | CTGCCTCAGCCTCCC[A/G]AATTGCTGAGATTAT | 83860 |
rs567856713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870911 | GTAATATGAAAAAAA[A/G]TTGTTTCCTATAAAG | 83860 |
rs567873796 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832392 | CTTTTTTTAAAGGCT[G/T]AATAATAATACTTTT | 83860 |
rs567874561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825655 | TCATTCATGTTGTAG[C/T]CTGTGTCGGGATTTC | 83860 |
rs567877380 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940331 | TAATTAAATCTAATA[A/G]ATATTTAAGCACCCA | 83860 |
rs567882308 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7946209 | CACACTCTTTCCCAT[G/T]ATCCATGAAGCTCTC | 83860 |
rs567898870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923854 | CAGAAAGCAAGGCAA[A/G]ATATCTTAAGAAATT | 83860 |
rs567907172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872006 | AATTTAATCGGGACG[C/G]TTTTCACATGTCAAG | 83860 |
rs567917096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7958750 | CATAACTTCCACGCG[C/T]GTTACTTATTCCTGC | 83860 |
rs567962199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915845 | TTAGCTGGATTTGGT[A/G]GTGGGCACCTGTAAT | 83860 |
rs567966963 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897619 | CTGTTTTATTTTCGC[A/G]TAACTTCCTTTCTCC | 83860 |
rs567970021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861936 | TTAAACTTGTGTTAG[A/G]CCTTTTGATATTGTT | 83860 |
rs567998386 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932166 | TTTTAAAAAGTAAAA[A/G]GAGGTGAACATGCTA | 83860 |
rs568000442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903729 | CTTCTCCTTTGAATT[A/T]AATCATCTTTTCCAG | 83860 |
rs568023441 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7820968 | GCTAGGCTAGGCATA[C/G]TCCAGATTATGTTTG | 83860 |
rs568054539 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956791 | CTGTGGCCATTTCTT[A/T]TTTGAAGTATAGCAT | 83860 |
rs568082284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7910836 | ACAAACCAGACTAGA[C/T]TTTTTAAAAAATAGA | 83860 |
rs568094730 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7923606 | AAAACAAAACAAAAC[-/A]AAAAAACCCCTCCCC | 83860 |
rs568098258 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878734 | ATGTATGTATGTATG[C/T]ATGTATGTATATGAG | 83860 |
rs568117995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7881917 | CACCAGAGACTTTAT[A/G]TGTTGGTGGACTTCC | 83860 |
rs568124858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7973631 | TACATGTTTGTTTTT[A/T]AAAAACCTTAATGAG | 83860 |
rs568125079 | snp | C/G | 3.33517e-05 | 0.00408347 | missense | TAF3 | GRCh38.p7 | 10:7964597 | CAGGTAAAACAAATA[C/G]AGACACCCCCTGATG | 83860 |
rs568151189 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955333 | TAGAAATTAATTTCT[A/G]CATCTGCATACATTT | 83860 |
rs568157659 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896905 | GGAAGGCCCTTTTCC[A/G/T]ACCTTCTTTATTGGT | 83860 |
rs568161619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931830 | ACAAATGACTGACAG[A/T]TCCTACCTGCTCAAA | 83860 |
rs568171222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7891286 | ATTTATTTGCTTTTA[C/T]CTTGAGGTACTTTCA | 83860 |
rs568176519 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902477 | TGTTATTAAGAGTCC[A/G]GGCCAATATTGACTG | 83860 |
rs568184814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7869340 | CACACACATAAATAC[A/G]TACGTACATAGATGT | 83860 |
rs568209505 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7827832 | GGCATGGTGGTGCAC[A/G]CTTGTAGTCCCAGCT | 83860 |
rs568221213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7939414 | AGCTAGATTATCTTA[C/T]AATGTAGCCCGCCAG | 83860 |
rs568251454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996993 | GCCACTGGGCCCAGC[C/T]GAGGAGAGGGTTAGT | 83860 |
rs568256872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7951672 | GGGAGGGGAAGAATG[C/T]CTGTTCATTTTTACA | 83860 |
rs568272724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952499 | CCCAGGATGTAGCCA[C/T]AGAAACCCCAAAGTC | 83860 |
rs568280157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7874873 | CTAAAGAAATTATGT[A/G]TTGAGCTCGGGTTTT | 83860 |
rs568280752 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980062 | AATGGGGAGGGAGGT[A/G]ACAGATTCCTGTCAC | 83860 |
rs568295271 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858925 | GCTGGCCTCTTCAGC[G/T]TCTTCTGGGCTCTAT | 83860 |
rs568312500 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7996441 | CAGCCTGTCCAGTCC[A/G]TGAGGGAACTGTGCC | 83860 |
rs568314487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8004294 | CTCAAGCGATCCACC[C/G]ACCTCGGCCTCCCAA | 83860 |
rs568325287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875547 | CCTTCCAGAGCCAGC[A/G]GGCACGAAGGGGTTG | 83860 |
rs568348445 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7829742 | AGTAAAGTTTCTCTT[A/C]TATCCCCTCTTCCCC | 83860 |
rs568360055 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7886444 | TCATGAATATGTAAC[-/TA]TTTTTTTCTTTACAC | 83860 |
rs568361582 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8010776 | TTAGCTGGGCATGGT[C/G]GCACGTGCCTGTAAT | 83860 |
rs568377484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8003541 | TCATAGTGCTAAACA[A/G]AGCAATAAATTTTAA | 83860 |
rs568395556 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005509 | TGGGAATCCTTAGTG[G/T]CGGGAGGGAGTTCTA | 83860 |
rs568401367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966730 | TGACCTGCAGCAGAT[A/G]TATTACCAATAAATT | 83860 |
rs568409335 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7867655 | GACAGGATGGCTACT[G/T]GCAGTTTTTGATAAG | 83860 |
rs568421278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7933978 | CTGCACACATGCACC[A/G]AAACCTGCAGAATGA | 83860 |
rs568426449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981267 | CCTCCTCCCTCTTCC[A/G]TCTATTCACCCACCC | 83860 |
rs568449419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877002 | CTTCCTTTACTCAAA[C/T]TGCCCACTTTCCTAT | 83860 |
rs568458650 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003487 | TTCCAAATGACCAAT[A/G]TATGACATTATAAAA | 83860 |
rs568486111 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7989004 | GTCATTTTATAGATT[C/G]TTTCCTGGTGTTTTA | 83860 |
rs568505050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7989559 | GCGTAGTCAAATGTA[A/G]TATTGTTTTTGCACA | 83860 |
rs568520291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7953549 | TTGGCTCTGTGAACC[A/G]ATCCCAGGTGTCATT | 83860 |
rs568523483 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911948 | ACTTAAGTTTAAAGC[C/T]CTTACTTTAAATCAT | 83860 |
rs568542599 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991701 | CATGCTCTAAATAAG[A/T]ATATATACACTATAT | 83860 |
rs568545335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904919 | CTTCCTCCACCACCC[A/G]CTCCTCCTCCACACT | 83860 |
rs568549989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823297 | AAATGTAACCAACAT[C/T]GACTTTGTCAGCACA | 83860 |
rs568599157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011715 | TGATCAGGAAAGATT[G/T]TGTACTTAACCTCCT | 83860 |
rs568620765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012502 | GCACACAGAGTCACG[A/G]CCTTCTGACTTCAAG | 83860 |
rs568627967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897763 | CTCCTGGGCTCAAGC[A/G]AGCCTCCTGCCTCAG | 83860 |
rs568634479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8010322 | AAAGCTTGTTTTTAT[A/G]TTGTTTTGGGATATG | 83860 |
rs568634930 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7848568 | CCTGGTCCCTCGACA[C/G]CTGCTAGATATCCTG | 83860 |
rs568641797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883583 | ACTTTTACCTACTAG[G/T]TTATCATCCATTGGT | 83860 |
rs568684777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7835784 | TTGCTTCTCACTGTT[C/T]CCCTTGCATAGATGC | 83860 |
rs568705114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876388 | ATTAGGAACCCTTGT[A/G]AAGAGGTATTTTCAA | 83860 |
rs568715575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952636 | GCATTTTAGTTTTTT[A/G]TTGTGCAGAATGTTA | 83860 |
rs568737892 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885514 | TGCCCCATTTCCCTC[C/G]TCACCGAATCCTTTC | 83860 |
rs568743704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7939425 | CTTACAATGTAGCCC[A/G]CCAGTTAGCAAAGTC | 83860 |
rs568781071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884220 | TTCACTGCTTCAGCT[A/G]TACCCGGTTTGGCCC | 83860 |
rs568783091 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7840543 | AAAAAAAAAAAGATT[-/G]GTTTTTTTTCTAAAT | 83860 |
rs568798123 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816653 | TTCTGCACACTATGG[C/T]ATTGGCTTGGCTGAG | 83860 |
rs568861951 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7956174 | ACAACTTTTCTACGT[G/T]TGAAATTATTTCAAA | 83860 |
rs568862205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856372 | GTAATCCCAGCTACT[C/T]GGGAGGCCGAGGCAG | 83860 |
rs568890921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960070 | ACCATAACATACTCT[A/G]AAGACCCGTTATCCT | 83860 |
rs568894659 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858137 | ATCCCATAGTAAAAG[A/G]ACTATGGGATGTAGT | 83860 |
rs568922203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828443 | TGTTTAGAAGTGAGA[C/T]CTCTTTGAAAATATT | 83860 |
rs568929621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898510 | TAGATCACGCCACTG[C/T]GCTCCAGATTGGGCG | 83860 |
rs568938878 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7929822 | AAAGTGGTAAGATGG[-/A]AAAAAAAAATGTCCA | 83860 |
rs568957367 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856210 | AAGATTTTGGCTGGG[C/T]GCAGTGGCTCACGCC | 83860 |
rs568980469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7973262 | ACACACAACTCAATA[A/G]TAGTAGAGCAGAATT | 83860 |
rs569015195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7925417 | GTCCTGATGACAATG[A/G]TAATATGGAGGTGTT | 83860 |
rs569018625 | snp | C/G/T | 3.33902e-05 | 0.00408586 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965544 | GGTCCCAGCCATGCT[C/G/T]CCATCTTTGTTGCCA | 83860 |
rs569037422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857632 | CATCCTGTTTGTGAG[C/T]TATTTCATGAAAGGG | 83860 |
rs569038648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835473 | CACCACTTTTACCTG[A/G]ATCTTCTCTTCCCTT | 83860 |
rs569063764 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841143 | GGCGTGAGCTGCCGC[A/G]CCCGGCCTAGAGCTT | 83860 |
rs569067310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954661 | GAGTGCACTCCATAT[A/G]TGAATGAGTGGATTA | 83860 |
rs569074880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997396 | GGATCATTAAACTTC[A/T]TGTGCAGACATATCC | 83860 |
rs569087108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998211 | ACTTTAATGTTTTTT[A/C]TTTTACTACTCAGAA | 83860 |
rs569098760 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7829496 | TTTGACGACCTTGAC[A/C]GTTTTGAGGATTATT | 83860 |
rs569099140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868445 | AGTGTGACATAGCAG[C/T]CAAGCTCTAGTGACC | 83860 |
rs569121534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7822471 | TTAATGCATCACAGA[A/G]GTAACCCATACTTAT | 83860 |
rs569126915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961661 | CAACACTCTTTCTCT[C/T]ATGCACTCTGTCCTG | 83860 |
rs569127111 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973707 | AGCTTGTAAATGTTT[C/G]TTTATTTTTGTTATA | 83860 |
rs569128637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954152 | CCAGTTAACACAGAG[C/T]TCTCCATAGTGAGAT | 83860 |
rs569132081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953201 | TTTCCCAGTCTTCTC[A/C]CTTCAAAAAGTAGGG | 83860 |
rs569197934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919386 | GCTGAAATCTTGCAG[A/G]GTGTACTGTCCTGGT | 83860 |
rs569201402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926544 | TGAGATTAGCTTTTT[A/G]TATGTGAACAATTGT | 83860 |
rs569203815 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005795 | ATATAAATGCCATAG[C/T]GATAACTTTGAACTC | 83860 |
rs569211493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7830673 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 83860 |
rs569218367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926919 | GTATTTTACTGTTTG[G/T]TTCAACGTGTGTATA | 83860 |
rs569245342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870026 | TTTCAGGTGAGCATC[A/T]TTAAAAAAATTAGAT | 83860 |
rs569295330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833990 | CGGCACAGGACAACA[A/G]CCAGACTGTTCTTTC | 83860 |
rs569298593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7863879 | CGTAAATATTTCATA[C/T]TTTCAATGTTTTACA | 83860 |
rs569299580 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7873231 | GTATTTTCTTCAAGA[-/T]TTTTTTTTTCTAACT | 83860 |
rs569317351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912656 | TTAGAAATCTTTGGG[A/C]ATTTGTAGGTTTACT | 83860 |
rs569319629 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7970020 | ATTCTGGCTTCAGAG[C/G]CTTTCTCTTCTGCCT | 83860 |
rs569320824 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817239 | CTGAAAAATGTCTCA[C/T]AGATTTAGCAACACA | 83860 |
rs569341651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7982754 | CAGGAGAGAGTTTTT[C/G]AAGGCAGTAAATTTA | 83860 |
rs569377233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7905712 | TAGTGAAACCCCGTC[C/T]CTACTAAAAATACAA | 83860 |
rs569384188 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003005 | TTTCTTTGTATTTGT[A/G]TACATCTTTTTATAG | 83860 |
rs569392180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890997 | CATGTAGCTGAACTT[A/G]CGGATGCCAGTACAC | 83860 |
rs569408022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005776 | GAGAATGCTTACCCT[A/C]TGGATATAAATGCCA | 83860 |
rs569408519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842543 | CTAAAAGATTAAACA[A/G]TAACCTTAAATTTTT | 83860 |
rs569442297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860841 | GTCTCGCTCTGTCAC[C/T]CAGGCTGGAATGCAG | 83860 |
rs569442352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7866694 | AGAGTTTTAAGTTAT[C/T]AGAAAGGAGAGCTAT | 83860 |
rs569446278 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982419 | CTTTTTTTTGAGACA[C/G]AGCCTCCCTCACTCT | 83860 |
rs569456481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008213 | GCGATTCTCCTGCCT[C/G]AGCCTCCTGAGTAGC | 83860 |
rs569473305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7957597 | AGAAGATGAACTTGT[A/G]TGAAAACTTACAACT | 83860 |
rs569497462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884398 | CTCTGCCTCCTTTTT[G/T]TTTTTGAGATGGAGT | 83860 |
rs569497947 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013410 | TTTACATAGTTATAG[-/T]TTTTTTTTTTTATGA | 83860 |
rs569532432 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924023 | TTGAAGTCTGTAGTT[C/G]ACAGTATTTAGGCCA | 83860 |
rs569532496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8013460 | TGTTCACAGAGATGA[C/T]TATAAAATGCTTTTT | 83860 |
rs569556727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7884949 | AGAAAACAGTTTCAG[A/G]ATTGCTAACCCATAC | 83860 |
rs569557102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877072 | ACGTCTGAGGTTTAT[A/T]TTTTACGCTGTTACT | 83860 |
rs569560414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978514 | AATTTCCACATTACT[C/G]TTTTCGGTTGTGCCA | 83860 |
rs569562573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830922 | CACTCATAATGCAGC[A/T]CAATGTGTTTCTCAA | 83860 |
rs569617108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833512 | TTTGAGGAATGTCTA[C/T]TCATTTTTTATTGGA | 83860 |
rs569617587 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7840785 | AGTGTACTCATTGCC[-/T]TTTATTTAGCTAATG | 83860 |
rs569620260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877890 | TTATTTTGAGAAGGG[A/G]CTAGTTAATTTCTAT | 83860 |
rs569620646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826232 | AATGATACTAACACA[A/C]CGACAGCCCAGAACC | 83860 |
rs569635820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839719 | ATTGTGTTTTGTTAA[C/T]ATCTTATTCTTCTAT | 83860 |
rs569637325 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824799 | GTAAAGTTCAAGTAG[A/C]GGAAAACAGTGAAGC | 83860 |
rs569646900 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002849 | CAGTTTTTGCTTTAT[A/G]TGTTTTGCAGATGTT | 83860 |
rs569662954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970658 | AGCACCTGTTTAACC[G/T]CCATATTTTAAAGAG | 83860 |
rs569663240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820093 | TACCTGCCTTTTCCA[A/G]AATGTTTTAAGCTGT | 83860 |
rs569677005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888618 | CATGCCCAGTTAGGT[A/G]CATTTACAGGTTATG | 83860 |
rs569677987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929345 | AAGGAATGATTGTGT[A/G]AAGTAAGATACATAC | 83860 |
rs569698776 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855376 | TGATAACACACCAGA[C/G]CAGAAGGCAGGGATG | 83860 |
rs569706391 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828350 | CTTGACTGAGGAGCT[A/G]TGTGATTATCCGCAG | 83860 |
rs569712887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915115 | CCAGCTACTTTTTTG[C/T]ATTTTTAGTAGAGAC | 83860 |
rs569729749 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7845729 | GTATAATCTCAGCAT[C/T]ATTTTCAATTGGCCG | 83860 |
rs569733271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7986373 | CCCAGCATTATTTCC[A/G]CCAGTGTGGTTCTTC | 83860 |
rs569740352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889339 | AACTAATATTCAGTA[A/G]AACATGCTCCATGCC | 83860 |
rs569774233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915598 | CAGTGAGTTGAGATC[A/G]CGCCACTGCACTCCA | 83860 |
rs569799804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7882808 | TTTGTAATAATTTCA[A/G]ACTTACAGAAAAGAT | 83860 |
rs569810630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8002037 | TTGTAAGATAGAAGA[C/T]GTTTCCCTTGAATAA | 83860 |
rs569857423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7957098 | TCATATCACTATCAA[C/T]TTTAACCAAACTTTA | 83860 |
rs569892650 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827342 | TTTTTTGTTAACACA[C/T]TTATATAAAATTGGA | 83860 |
rs569897001 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7881253 | TCAAAAAAAAAAAAC[A/C]AAAAAAAAACCCACA | 83860 |
rs569905690 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8017052 | AGTGGCCTGTGTGAA[A/G]TGAACTGGTGGTCTC | 83860 |
rs569906128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861258 | GTGAGCCACCGCATC[C/T]GGCCCTGCACGGCTA | 83860 |
rs569913329 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014479 | TGTGATCTCATAGTC[C/T]GCATGCCCAACAATA | 83860 |
rs569920084 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868583 | TGGATTCACATCCTG[A/G]AGCAGCCTGTTAGTA | 83860 |
rs569979783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872746 | ATAATTTCTTTTTCA[C/T]GCTGCCTTAAAATCA | 83860 |
rs569985254 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953629 | CCTTGATGTGGCTCC[A/G]TGTGTACCTTGTGCA | 83860 |
rs569995757 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7896588 | ATTTGGGGACAGATT[G/T]AGCTAAGTTGCAGTA | 83860 |
rs570005484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945523 | TTCTAGTTAAGTGGA[C/T]TCCCTTTGGCCGCAG | 83860 |
rs570030561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855412 | CTGAAAACAAGGGGG[A/T]ATTCATGGAATGTGA | 83860 |
rs570038313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937927 | AACAGAACCCGCTTT[A/T]AAGACCAGTCAGTGG | 83860 |
rs570058671 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944547 | ATAGCAGGTCTAACT[C/T]TGTCTGAGATAGAGC | 83860 |
rs570059763 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836504 | GTCTTGAACTCCCGA[C/G]CTTGGGTGATCTGCC | 83860 |
rs570095288 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980692 | TCCAGCCTAGCAGAA[A/G]CCTTGCCTTGATGCT | 83860 |
rs570128633 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946650 | ATCACTTGGACCCAG[A/G]AGGTGGAGGCTGCAG | 83860 |
rs570156890 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835822 | TCGGGTCTCATGGCG[C/T]TTGGTGGCATGTTGT | 83860 |
rs570162907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7972606 | ATTCAACCAGTTGAC[C/T]GAATACCTGTTGCCT | 83860 |
rs570187618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902777 | TTATTGATGATTCTT[A/G]TCAGTTATTATACTT | 83860 |
rs570210023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7854630 | GATTTAAATTTCAGT[A/G]AAGAGAACTGAAAAG | 83860 |
rs570213737 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849493 | ATTTATGTTTCATAA[A/G]CATTGTATGTAGGCT | 83860 |
rs570220269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980119 | ACACCTTGGGGGGGA[A/T]TAATACTCTTTTGAA | 83860 |
rs570222909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929934 | GGGCCAGGCGTGGTG[G/T]CTCACACCTATAATT | 83860 |
rs570234994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909241 | AGCCTCTGGGGCCCA[C/G]GCTCTGGGTTTCTGA | 83860 |
rs570308045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931906 | AATGAATTCATTACA[A/G]TGTAATGTGGCAGAT | 83860 |
rs570321148 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861407 | CACCGCACCCAGCCA[A/C]CAGGAGCCTTTTCAT | 83860 |
rs570322842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7899045 | GGTGAGATTCCCCCA[A/G]TCTACCTGGAAGGGA | 83860 |
rs570328787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915807 | AACATGGTGAAATCT[C/T]GTCTCTACTAAAAAT | 83860 |
rs570346502 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8006735 | TCAGTGCCTTTTGGT[-/G]AAAGTGGTTTCTAAA | 83860 |
rs570357161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7834039 | CCTTATATATTTTGC[C/T]TTTTTTTTTGGTGGT | 83860 |
rs570370578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938387 | GGCAATGTGATGGGC[A/G]GGCCTCGCCTAAGGT | 83860 |
rs570381844 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896341 | TCTGGGGATGGTTGT[A/G]AGTTCTAATGCTGTC | 83860 |
rs570464245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7882861 | CTAAGTATTCTTTAC[A/G]TAGATTCCCCAAATG | 83860 |
rs570520792 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7980257 | GAAAAAGCTTTACAG[C/G]GTTCAAATTATACCT | 83860 |
rs570529904 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881623 | CAAGACACCTTCTAT[A/T]TCTAGGGGGCCCCTT | 83860 |
rs570534143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839842 | TGTCTCTTGCTTTAC[A/G]TTCAGGCCAGCAAGA | 83860 |
rs570539503 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977994 | AGGCCTACAGTACTC[C/T]TACCTGATCCTAATA | 83860 |
rs570548474 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7923649 | TGGTTTTCATCCTGT[A/G]TTCAATAGAGTAGCG | 83860 |
rs570553793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861820 | CTTGGGAGTTACTGA[A/T]CTTCTTTAATGTGTA | 83860 |
rs570561323 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953827 | CTCTCCATAGTGAGA[C/T]TCAAGAGTGCACGCC | 83860 |
rs570562938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7902859 | TTAAGAAAAAAAGAA[C/T]TGTCTCTCTTCCACT | 83860 |
rs570563746 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922874 | AAAGCAGTTAAAATG[A/C]ATAATTGGAGCAGTG | 83860 |
rs570625676 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920072 | GCAACGTAGGGAGAC[C/G]CATTCTACAGAAAAT | 83860 |
rs570634974 | snp | C/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948976 | CCTCAGAGGGACTGA[C/G/T]GCGCAGAGGTGCTGG | 83860 |
rs570658952 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TAF3 | GRCh38.p7 | 10:7892295 | GTGCTGCCTGTTGGG[A/G]GCTAGAAAGCATGCT | 83860 |
rs570659695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868483 | GTGGAGGTGGTGTGA[C/T]ATAGCGGCCAAGTTC | 83860 |
rs570665519 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879377 | CATACTCATGCATAA[C/T]TGATTATATATTTTA | 83860 |
rs570669180 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7840531 | TCCAGAATGAAAAAA[A/G]AAAAAAAGATTGGTT | 83860 |
rs570677546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923121 | TGTATTTACATTCTA[C/T]TATGAGTATGACAGA | 83860 |
rs570685263 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003222 | TCTCTCTCTCTCTTT[C/T]CTTTTATCAGACCAA | 83860 |
rs570695411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011027 | GTTTATACAGATTAC[A/G]TTCTTTGGATACTAT | 83860 |
rs570700030 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906778 | TATTTTGTAAAGGAG[A/C/G]ATCAGTTGAGCCCAG | 83860 |
rs570717852 | snp | C/T | 0.000399281 | 0.0141238 | missense | TAF3 | GRCh38.p7 | 10:7965186 | AGGAGAAGGATAAAG[C/T]GAAAGAGAAAGAGAA | 83860 |
rs570730016 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | TAF3 | GRCh38.p7 | 10:7974142 | GAAACATACACACAC[A/T]CACACACACACACAC | 83860 |
rs570734978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873663 | ATTTGAGGGGAGTCC[C/T]CCACTCCCTTGTCCT | 83860 |
rs570735508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835173 | AGAAGGATTGTCTTT[A/G]GCCACACATAAAATA | 83860 |
rs570763054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7847583 | TGGGTAGCTGGAACT[A/G]CAGGCATGTGTTACC | 83860 |
rs570775155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890134 | ACTCTCAGTCACTTC[G/T]CTGGGACTTTTCTCT | 83860 |
rs570779650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8009404 | GTGCTCTGAATCACT[A/T]TCGAATTTCAGACGC | 83860 |
rs570792743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938503 | GATGGTGAGTGGGAA[A/G]GCTTGAAAACTCATG | 83860 |
rs570797701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7939131 | GGGATGTAAAAGATA[A/T]AAAAGTCTGTTTGTG | 83860 |
rs570803955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841967 | TTGCTTATGTTAAGG[A/G]CAGCAGGTACACTTG | 83860 |
rs570826430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7844452 | CGCGATCTCGGCTCA[C/T]TGCAACCTCCGCCTC | 83860 |
rs570840484 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7883530 | CTATCTGGTGGAGAG[A/T]TACTTTGAGACTATG | 83860 |
rs570857258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7981089 | AATTCAGGTAAAGGA[A/G]CTTTGTGAGAAAAAG | 83860 |
rs570864419 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899367 | TGGCTTCCAGCACAC[A/G]CATTCAGCAAGTCCC | 83860 |
rs570864862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835630 | CCATTGGATCTCACT[C/T]AGCCCCTTGTACTCC | 83860 |
rs570888828 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7996352 | GCTGTCCCCATAGAA[A/G]CCACAGCCTGTTTTA | 83860 |
rs570893486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996831 | ACTACAGGCACGCAC[C/G]ACCACACTCTATTTT | 83860 |
rs570902481 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846688 | GTCACCAAATATCCA[C/T]TGGACCTCCTATAAA | 83860 |
rs570916917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7983634 | TCCCTGATTAACTTG[A/C]TACAGAAACTGAAAC | 83860 |
rs570924989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7886534 | ATTCTAGCTTTGCCA[C/T]GTTGTGGCTATATGA | 83860 |
rs570963256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829598 | ATGAGATCTTGGGGA[C/G]AAAGACCACAGAGGT | 83860 |
rs570972544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966263 | GTCTACAGAACTTTC[C/T]GTAGCATCTTTTATT | 83860 |
rs570980030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991539 | AGATATAATATTAAA[C/T]AGGCAATCTCAGAGC | 83860 |
rs570983866 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875404 | CTTTCTGGCTGAATA[C/G]TGATAATTTTTCCTC | 83860 |
rs570996431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879454 | AAATAATGACACCCA[C/T]CCTCATCTTTGTACA | 83860 |
rs570998697 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845961 | TTTGTGTGTTTTTGT[-/T]TTTTTTTTTTTTTTT | 83860 |
rs571026370 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7903636 | TGCAGTTTAGCATTG[C/T]ACCATATATGAAAAA | 83860 |
rs571043014 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7926269 | AATATATCAAACTTT[A/T]TTTTTATTACGCCAA | 83860 |
rs571044996 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831410 | GAGTGCAGTGGCTCA[A/G]TCTTGGCTCACTGCA | 83860 |
rs571045464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889408 | CTTCACAACAACCCT[A/G]TAAGGCAAATACTAT | 83860 |
rs571058310 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7880181 | GAGTTCTAGGCTGCA[G/T]TGAGCTATGATCACT | 83860 |
rs571062272 | in-del | -/TGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901466 | GTGCTTGCTATTTAA[-/TGT]TGTTTTTGACCAACC | 83860 |
rs571062896 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852201 | GAGATCCTCTTGCCT[C/T]AGCATTCAAAAGTGC | 83860 |
rs571073304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841219 | GTGGTTATATACTGA[G/T]GGTGTGCCATTGGTG | 83860 |
rs571080911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896782 | GAGTTATTTTCAACA[C/G]TTTCTGTAGGACAGA | 83860 |
rs571088132 | in-del | -/AA | 0.0283406 | 0.115616 | intron-variant | TAF3 | GRCh38.p7 | 10:7905882 | TGCAAGAATCTGTCT[-/AA]AAAAAAAAAAATTTA | 83860 |
rs571096651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8014383 | GATAAAGACAAAGCC[G/T]TGGCTCGGAAGACTT | 83860 |
rs571130289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7942221 | CCCGTGACGATGCAT[A/G]AATTGCGTTTTGTCG | 83860 |
rs571132154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7844988 | TTATTTCCTTATGAT[A/G]AATTCCCAGGGTAGA | 83860 |
rs571148155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7897569 | TGGGCTCTTTTAATC[C/T]GATAATCCATACCCT | 83860 |
rs571154320 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923217 | GAACAGAAATAGAGC[A/G]GTGTCTCATTCAACT | 83860 |
rs571159674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7851371 | TCAGTGTGACTGGAA[C/T]AGGGGGTGGTTGGGG | 83860 |
rs571174158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7932867 | ATTTTTTTGTGTGGA[C/T]GGGGATCTCAATATA | 83860 |
rs571192450 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976568 | TACAGGCGCCCGCCA[C/G]CACGCCCAGCTAATT | 83860 |
rs571192591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949034 | GCTGCTGCCGCCGCT[A/G]CTGACAGCCGCTCTC | 83860 |
rs571198637 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7838700 | CTGGTTTTCTTAATG[G/T]GCAGGCAGGCTTCTT | 83860 |
rs571217502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7999690 | TCAAACTCCTGACCT[C/T]AGGCAGTCCTCCTGC | 83860 |
rs571225066 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8000343 | GCTGGTCTCGAACTC[C/G]CAACCTCAGGTGATC | 83860 |
rs571258368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941688 | CTGTTAGGTCGGGAA[A/G]ATAGTAAGTTCTCAT | 83860 |
rs571276060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7908598 | ATCTGGGTTACCGAG[C/T]GCTTCTGAAGGAAAG | 83860 |
rs571318994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948304 | TTGTTGCCCAGGCTG[G/T]TCTTGAACTCCCAGC | 83860 |
rs571328185 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817962 | ATTTTTTTAAAAAAA[A/C]TGTTAAAATATTATC | 83860 |
rs571334498 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958709 | GCAGGCGATGGCCTC[A/G]CAGGTGTTCACTGAT | 83860 |
rs571432774 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014925 | TGTTCACTCCCGAGC[C/T]GCCTTGGCCTGTGGC | 83860 |
rs571442082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7900464 | GCTACTCCTCGGTGG[A/G]TGGCTGGAGAGAGCT | 83860 |
rs571479929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7937169 | GGTTTTTGTGGGGAC[A/G]TAAGTTTTCAGTTCA | 83860 |
rs571500770 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944123 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGT]TGTGGGGGGGAGGGA | 83860 |
rs571512830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928428 | GTAGTTTTACCTTTT[A/G]TGTCAAAAAATGCCA | 83860 |
rs571577942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949682 | CCATTCATTTATGTA[C/T]CACTAAGGTAAAAAC | 83860 |
rs571609613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8001157 | TTACACAGCTGTCTA[A/T]TGTTGCCTCAGGATA | 83860 |
rs571612463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908004 | GTAGAAGAAGTTGGC[A/G]GTGGTGCAGATTTGC | 83860 |
rs571622510 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968543 | AGAAATAATGATAAG[A/G]ACACTAAAAACAGCA | 83860 |
rs571625892 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821455 | AGATACAATCCCTGA[A/C]CATAAGGTGTGTTCA | 83860 |
rs571642162 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7894564 | TGATTTTTAATTGGT[C/G]ATTGTTTGAAGTTGG | 83860 |
rs571655860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860666 | CAAAAGGTACCAATT[A/C]AATTTTTATATCATT | 83860 |
rs571662132 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989609 | GATTCTAAATTAAAA[C/T]TTTTGATAGAAATTA | 83860 |
rs571666974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7845802 | TGATTTTTAACTTAT[A/G]TGAATAGCATTGCTT | 83860 |
rs571688478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7956216 | AAAAATAGGCCGGGC[A/G]CGGTGTCTCACGCCT | 83860 |
rs571694997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969857 | GCTCTGCCACTTACT[C/T]GTTATTCACCAACCT | 83860 |
rs571709763 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991581 | ACAAAGGTCAGGAGT[A/G]TGATATAGATTTATA | 83860 |
rs571721591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853723 | TTCCATATTATGGGT[A/G]ACTGCTTTGGCACTA | 83860 |
rs571725294 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7871992 | ATTTCAAAACTATAA[A/C/G]TTTAATCGGGACGCT | 83860 |
rs571789382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914339 | CTTATGTTAACCCCT[G/T]GGGGGAGATATTTGA | 83860 |
rs571791218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913966 | TTCAACAAATCAGTG[G/T]CATGAAAAAAAGAGA | 83860 |
rs571801767 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915369 | AGAATCATGGGCCGG[A/G]CGCAGTGGCTCACGC | 83860 |
rs571812027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865452 | CCTCTGCACTCCAGC[C/G]TGGGGGACAGAGTGA | 83860 |
rs571816335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7994689 | CTGAGTCTTGGCCAG[C/G]CACAGTGGCCCACGC | 83860 |
rs571833520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975485 | AACAGCTAGTATTGG[A/T]GGCATACATGAAGCT | 83860 |
rs571837794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818922 | CCCGGCAAGTCAAGG[A/G]TGACACCTTCGCTCT | 83860 |
rs571851992 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917261 | GGATGGAGTGTCAGA[A/G]AGGAGTTGCAGTTGG | 83860 |
rs571885921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8000697 | GGTGGGAGGATCAAA[C/T]AAGCCTGGGAGGCAG | 83860 |
rs571905249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943213 | CTTGAATGAAACAGG[C/T]GCTCGATGTTGGCCT | 83860 |
rs571939454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878277 | TGTCAGTAGTAGACT[A/G]GGTAAATAGATTGTG | 83860 |
rs571974316 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945237 | AATGTGAACAGAGGG[A/G]TGCTAATCCTGTTTG | 83860 |
rs571992798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7913509 | AACCCATTTATTATG[C/T]CACAGTATTTTAAGA | 83860 |
rs572004680 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894372 | ACATCAAAATCCATC[A/G]AGTACTCGTTGCCTG | 83860 |
rs572006706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7920624 | TGAATTTGTACGATA[C/T]AAATCCCTTATCTTT | 83860 |
rs572037917 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7863114 | GAAAATCCAGGAAAC[-/TG]TGGTGGACTAACTTC | 83860 |
rs572038948 | snp | C/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014839 | GCAAGTCTGCCGTCA[C/T]ATCCACCCCCAGATG | 83860 |
rs572048547 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7935333 | CCAGGCGCGGTGGCT[C/T]ATGCCTGTAATCTCA | 83860 |
rs572053362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825103 | ATAATGGTCAGTCCA[A/G]TTGCAGAGTTCCCTT | 83860 |
rs572082816 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825374 | ATGGACCATTGTAAA[C/G]GTGTGCAGTTCTGTG | 83860 |
rs572087315 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968742 | AAGTGATTGAACAGG[A/G]GCCAAAATTTCAATC | 83860 |
rs572089442 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7858832 | TGTGTGTGTGTGCGC[A/G]CGCCTGCATGTCACT | 83860 |
rs572100938 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010758 | CTAAAAATACAAACA[A/G]AATTAGCTGGGCATG | 83860 |
rs572117229 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818313 | GCGTTTTCGTCACCG[C/G]TGTCCCCCAGGTGAG | 83860 |
rs572125968 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898451 | CTTGGGAGGCTGAGG[C/T]AGGAGAATCACTTGA | 83860 |
rs572164059 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7885382 | CCATTTATATTTCTT[A/T]TTTAGGCTTTCCTCT | 83860 |
rs572167033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7922427 | AAGCCTCTCTTTTCT[A/G]TAAAACATAGATGAT | 83860 |
rs572176726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886097 | CCATGTCTGGCTAAT[G/T]GTTTTTTGTAGAGAT | 83860 |
rs572179754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818998 | CGAGATCTGCTGTTT[C/T]CTCGGCCTCCCACGT | 83860 |
rs572222439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8001257 | CTGGACCAACCATCT[C/G]TCCCTTTCCCCTAGC | 83860 |
rs572224096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962571 | ACTCTACTTTCCAGA[C/T]AAATAATTTTCTGTT | 83860 |
rs572228356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7914894 | GACCACATGTGCCTG[C/T]CACACCTCATGCCCC | 83860 |
rs572228601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7923304 | GATGTAATTTAAAAT[C/T]GCTTTGTTTCACATC | 83860 |
rs572237141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7892970 | GATTATAGGCATGCA[C/T]CACCACACCCCATTA | 83860 |
rs572254369 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947441 | ACAAAAAATAGCTAA[G/T]CAAACATTCTGTGGT | 83860 |
rs572256544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8014425 | TGAGAGGATGAATGA[A/G]CGGATGAGTCTCTGC | 83860 |
rs572270759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7832325 | TGGCTTACTTCACTT[A/G]GCAGAATTGTTTGAA | 83860 |
rs572279938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7900805 | TCTTTAGGCTTCGTA[C/T]TAAGAAGGTAAAGAT | 83860 |
rs572281671 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TAF3 | GRCh38.p7 | 10:7954905 | AACACAGAGCTCTCC[A/C]TAGTGAGATTCAGAG | 83860 |
rs572339128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893916 | AGACCCCTTAAGAAA[C/T]ACAGAAAGAGGCAGA | 83860 |
rs572341284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7901537 | GTAGAAAACAGTATT[A/G]TGTGTGGCTGTTTAG | 83860 |
rs572345039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7961970 | CCCTTGCACCTCAGT[C/T]TCCCAGGTAGCTGGG | 83860 |
rs572368663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880590 | ACATAATCCTGCTGA[C/T]GTTGTTTCCTTTAAG | 83860 |
rs572393319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919998 | TGCTGGTAATCCCAG[C/T]GTTTTAGGAGGGTGA | 83860 |
rs572401142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7840257 | TCATGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 83860 |
rs572402037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7894746 | ATTTTAGTATGCTTT[C/T]CCCTGGGCTGGAGTG | 83860 |
rs572411318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7833685 | TGGAGGAGCCAGGCA[G/T]TGGCACGGGCCATGC | 83860 |
rs572455140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7984866 | CTGATTATAATTTCT[C/T]CTAAAGATCAAACTA | 83860 |
rs572456450 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012709 | AGTTTTCCTGTCAAT[A/G]TAGTTTGCCTTTGTA | 83860 |
rs572470210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839401 | CTATGGTCCTGCTAC[G/T]CTATGAGAGTTGAAT | 83860 |
rs572471156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826424 | GGTAGTGAAGAAGTA[G/T]GAAAAACAATTTAGT | 83860 |
rs572504277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943282 | GGCTCCTACGCATCA[C/T]GTTCTGCTTGCTCCT | 83860 |
rs572506713 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888247 | CTGTCCAAGCACATT[C/T]TTTTGCTTCTTTACT | 83860 |
rs572518185 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903382 | GCACAAGAAGCCCCA[A/G]GCTCACTGTGTACTT | 83860 |
rs572523230 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010300 | GTCAGCCTCCATAAA[A/T]CATATCAAAGCTTGT | 83860 |
rs572526375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7834125 | GTCAGATGTGTGGGT[A/G]CACGTGTTTTCCTCC | 83860 |
rs572532227 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846108 | GGACTACAGGCGCCC[A/G]CCACCACGCCTAGCT | 83860 |
rs572546611 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944395 | TCTAGTTAGTCAGTA[A/G]GACCATCAACAGACT | 83860 |
rs572552584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873037 | AGAAATCTTATTTCA[A/T]GACTAAATTATAGAT | 83860 |
rs572561199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7852643 | GGGGGTGTGTAACTC[C/T]GTCAGAGTACACATA | 83860 |
rs572565589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949778 | TTTTAACTGCATAGA[C/T]CAAATACTTCAAATT | 83860 |
rs572615416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865663 | TGCAAAGTAGCAACT[A/G]GGTTCATTCTTAGAG | 83860 |
rs572617135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7873892 | ATTCTGTTGGCACAT[C/T]TGTATTGAGCACTTA | 83860 |
rs572660071 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866425 | TTCTCTGAGAAGGGA[A/G]CACTTAAGCTGATAG | 83860 |
rs572668520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7853308 | CTGTGCCTCTGAACA[C/T]CTCCCAACTCCACAT | 83860 |
rs572689958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7970783 | CCCCCAAATAATCTT[G/T]TATTAAATTTAAACG | 83860 |
rs572696315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886895 | CATCTCTAAGAGTAT[C/G]TTTAAATTTTATTTG | 83860 |
rs572740990 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TAF3 | GRCh38.p7 | 10:7896519 | AGATCTCTAGTTGCC[A/G]TAGCCCCACACAGCG | 83860 |
rs572760156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7939470 | TGTAGAGTGTCCAGC[A/G]ACTCACGCTTAAACA | 83860 |
rs572764000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7890537 | TTTGTTTTAAGATGT[A/G]TAAATATGTGCATTC | 83860 |
rs572777259 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989895 | ACTCTGGCTGTGATA[G/T]CATATACTTACCTGG | 83860 |
rs572777715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7938712 | GGAGGAATCTTGAAG[A/G]TAAAGATTTAGGAGT | 83860 |
rs572792000 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | TAF3 | GRCh38.p7 | 10:7842160 | AATATTGTTTTTTTT[G/T]TTTGTTTTTTTTTTT | 83860 |
rs572801413 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890684 | TTCAGTTTCTTTTAA[A/G]TGAAATTAGAACTTT | 83860 |
rs572803864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7933341 | ATCTTGCTCACTCTG[C/T]ATCTCCCCAGAGCAG | 83860 |
rs572805880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7897954 | GCATGAGCCACCACA[C/T]CCGGTCCCTATTTTC | 83860 |
rs572813448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7977906 | TTTTCATGGAATCAT[C/T]ATATCAACCCACTCG | 83860 |
rs572820935 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879974 | GGCAACTCTGGGAGT[C/T]TGCAGCAAGAGGAGC | 83860 |
rs572826950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883698 | CATTCTACTCTATGG[A/G]AGATTTTCCCCTCCT | 83860 |
rs572845580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884471 | GGCTCACTGCAACCT[C/T]TGCCTCCTGGGTTCA | 83860 |
rs572851083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954300 | GAGCTCTCCCTAGTG[A/G]GATTCAGAGTGCACT | 83860 |
rs572855384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997517 | TTACAGGCCAAGCAG[C/T]TCATGACCCATTCTA | 83860 |
rs572857224 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817402 | GACTTTGAAAAATGT[G/T]AATATCATGTTCAAA | 83860 |
rs572857230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947300 | GCAGGCCGGATAGTG[C/T]GGTTAAGAGCTTTCC | 83860 |
rs572922349 | in-del | -/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845976 | TTTTTTTTTTTTTTT[-/TT]GAGGCAATGTCTCGC | 83860 |
rs572952630 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7966445 | ACAAACTGATAGAAA[C/T]CCCGCAGTTTTGTAG | 83860 |
rs572963210 | in-del | -/AAAAACT | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7932091 | TTAGTTACTTCTTGG[-/AAAAACT]GAGTCTTAGAAATTT | 83860 |
rs572968304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876625 | ACAGAATCACGGGGG[A/T]CAGTGGTTATGTGAC | 83860 |
rs572969409 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7835336 | CTGTGGGTTGACAAG[C/G]TTGCTTTAGAAGGAG | 83860 |
rs572971501 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | TAF3 | GRCh38.p7 | 10:7850682 | TCCATCTCAAAAAAA[A/T]AAAAATATATATGTA | 83860 |
rs573031903 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7843454 | CTTCCATCATTTTTT[G/T]ATCTGCTTTTAGTTG | 83860 |
rs573047496 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936716 | CAGTTTACATTAGGG[G/T]TTGCTCTTGGTGTTG | 83860 |
rs573070253 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842700 | TTTAACTTTCTCCCC[A/G]ATAAGATATATCTGT | 83860 |
rs573076276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974524 | CAGGGATGAGATCAC[A/T]AAAGAAACTGTAGCA | 83860 |
rs573078221 | snp | A/C | | | upstream-variant-2KB, missense | TAF3, LOC105376392 | GRCh38.p7 | 10:7818479 | CTCGGCATTCGGCTT[A/C]TGCTGCCTCGCCCCG | 83860 |
rs573082953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830726 | TGACCTCAAGTGATC[C/T]GCCAGCCTCGGCCTC | 83860 |
rs573083092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7822933 | GGTGTTTTCTAATTA[C/T]ATTTGAAAATTTATA | 83860 |
rs573086143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7841594 | GAGAAGGATGGACTC[A/G]AGAGGAGATGTCACT | 83860 |
rs573086350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855981 | CTCTACTAGTATTCT[A/G]AGAGAGGACAAGAAA | 83860 |
rs573113382 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871887 | ACTATCCAAATATTT[A/C]TAATATTTGTTCATC | 83860 |
rs573118600 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7955879 | GAAATGGAGTTTGTG[C/G]TGTCCTGCTCCCATC | 83860 |
rs573127367 | snp | C/T | 0.00045138 | 0.0150162 | missense | TAF3 | GRCh38.p7 | 10:7964979 | TGCCCCCCAACTTTC[C/T]TTATATCTCTTCTCC | 83860 |
rs573137437 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908897 | TGGGCCCAGCCCCAG[A/G]GGTTCTGAGTCAGTG | 83860 |
rs573138551 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7973868 | GGCACGGTGGCTCAC[G/T]CCTGTTATCCCAGCA | 83860 |
rs573145946 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7823575 | TAGAAGTTTGAGGCA[C/G]CAAGGAGCTGTGATC | 83860 |
rs573149011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856390 | GAGGCCGAGGCAGGA[G/T]AATCGCTTGAACCCA | 83860 |
rs573164170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857932 | TTTTTTTTTTCTGCT[A/T]ACCTTAGGGATTTCT | 83860 |
rs573167744 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7941609 | CACTGTATCCTCATC[A/C]TCCTGGACATCCTTG | 83860 |
rs573194215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947841 | ATTCGGAGTTGGAGA[A/G]TCAATTCCAGCCTCA | 83860 |
rs573198663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012668 | CGGAGGGTCAGAGAT[A/G]TAGTTGCCCACAGAT | 83860 |
rs573200366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906382 | AGCTATCAGAAACAG[G/T]TGGTAACTACAGCTA | 83860 |
rs573240742 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997606 | CTTCTGCACGTTTTT[A/G]TGAATAACGCCAGTG | 83860 |
rs573251127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998791 | TTGCAGTGAGCCGGG[A/G]TCGCGCCACTGCACT | 83860 |
rs573262889 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7960929 | CCTCAGAAGGGGTTC[C/T]ACAAACCCTCAATTT | 83860 |
rs573272677 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990489 | AAATTTTGAATGACC[A/G]CTACATCTTTTTTCT | 83860 |
rs573314310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8005343 | AATTATCTGTATTAA[C/T]ATGAGACCTAGATTT | 83860 |
rs573320861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941771 | GAAAAGGGCAGGGTT[A/G]TGGTAGCTGGGTTTT | 83860 |
rs573326313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966857 | GTTCTCTTTGGCTAT[C/G]CTAAAATATAAAAAA | 83860 |
rs573326315 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979140 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGTCT | 83860 |
rs573337537 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920813 | AATTTGGTAGCATTG[A/G]AATAGAATTTTTGTC | 83860 |
rs573352683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934770 | TAATATTTAAAAGTA[C/T]TATGATATAGAGCAG | 83860 |
rs573354080 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7990241 | CGCTAATGCCATTAG[C/G]GTTATTTGTTCTGAA | 83860 |
rs573366798 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881402 | GCCTCCAAGTCAGCA[A/G]TATACGAAAACTTCA | 83860 |
rs573382566 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987437 | TGGTATTTCATTTTA[C/G]TGTTGTATCATCATT | 83860 |
rs573414067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7941402 | AGGTCAGCAGGGTGG[A/G]GATTATTTGTAACTG | 83860 |
rs573421409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7912201 | TATGAAGTTGAAGCC[A/G]TCTGTGTTAACTAAA | 83860 |
rs573422964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919131 | AAAATGGGAGATTGA[A/G]TGCGACTAGGGGCCA | 83860 |
rs573426254 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917168 | CTGGGGAGACAGACA[A/G]TATAAAAGTAAACAT | 83860 |
rs573429775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877144 | TATCTGTTACTTCCT[G/T]TTGGTAAACACAAAT | 83860 |
rs573433728 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7868984 | AACTCCATATTTTTT[G/T]CTAGCAAGGTCCTTC | 83860 |
rs573469702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7912726 | ATCATTTAATATTTC[C/T]CTACAAATCCAGATC | 83860 |
rs573471558 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936498 | GACCTGAGCTGCATC[-/T]TTTTTTTTTTTTTCT | 83860 |
rs573482980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7957754 | TCTTTGAAATATTTC[A/G]TATATACACATGCTG | 83860 |
rs573499240 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816954 | TAAATACAAAATATA[C/T]AGTAAATTGGCAAAA | 83860 |
rs573523535 | in-del | -/AT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850686 | CTCAAAAAAAAAAAA[-/AT]ATATATATGTATATA | 83860 |
rs573524609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857200 | GACTTTTTTGCTGAA[C/T]TGGATACTAGTTTCT | 83860 |
rs573548859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934199 | TACTTCACTTTTTTT[A/T]AAATGTATGGATGAG | 83860 |
rs573588324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7905316 | AGAGAAGCACCTGTT[C/T]CAGGGGAAGCCAATG | 83860 |
rs573632131 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821526 | TGTTTCTTCTAAAAG[A/G]AATGTTCTCAAGTTA | 83860 |
rs573635458 | in-del | -/AC | 0.461813 | 0.132798 | intron-variant | TAF3 | GRCh38.p7 | 10:7974134 | TTCCTTCTGAAACAT[-/AC]ACACACACACACACA | 83860 |
rs573638595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7878082 | AGGGAACGGGTATTA[C/T]GCATCTGACCTTCCT | 83860 |
rs573641629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7830735 | GTGATCCGCCAGCCT[C/T]GGCCTCCCAAAGTGC | 83860 |
rs573655298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941511 | CAGAGTTGAGTGGGC[C/T]GTGTAGTAATCAAGG | 83860 |
rs573675241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7862361 | TGCTGTTTTCCTGAT[A/G]TTTGTTTTTTGTTTC | 83860 |
rs573701454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870279 | CATTGGTTGTACTTT[A/G]GAACTACTGTATATT | 83860 |
rs573704823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7823594 | GGAGCTGTGATCATA[C/T]CACTGCACTTCAGCC | 83860 |
rs573726700 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7882845 | ATAGCACAAAGAATT[-/C]CTAAGTATTCTTTAC | 83860 |
rs573744255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012774 | AACATATATGGACCC[C/T]CAATGCACCTGTCAC | 83860 |
rs573758745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7869731 | AGCATGCACCCCTGC[A/G]GCAGCACGGACTGCC | 83860 |
rs573775940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946991 | GGTCTGGAACTCCTG[A/G]CCTTAAGAGATCCTC | 83860 |
rs573782802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012044 | TGGCTGGGCAGGGTG[A/G]CATGTGCCTGTAGTC | 83860 |
rs573784782 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914310 | TGGTTGGTTTCTCAT[C/T]CTTCAAGTATTGGCT | 83860 |
rs573811103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7942071 | TGTGCCTCCACTTCA[A/G]TTATATCTCAAGAGG | 83860 |
rs573816286 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924887 | CTTAAAACGTAAGTT[A/G]TTTAGAAAGTATAGA | 83860 |
rs573825912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7975299 | GATGTGTAGAAGGGG[A/G]AAGAAGGTCATGGGA | 83860 |
rs573851762 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TAF3 | GRCh38.p7 | 10:7883852 | TTATGGTTATGGCAG[G/T]TGGGAAGTACAAGGT | 83860 |
rs573883667 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817100 | GCAAATGAAGAGGAA[C/T]AAACACCCAGGGTGG | 83860 |
rs573885190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7926803 | GTTTAAGATTAGTAA[A/G]CAATAGTTTTTAAAC | 83860 |
rs573910126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948525 | GTTGATTGTAATTTC[A/G]TAGCATTTTTCTCAT | 83860 |
rs573913721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7974726 | TGTGAGAAATTGTTA[C/G]CTAGAGGTTGAAGAG | 83860 |
rs573922292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900038 | CTTCTTATTTGCCTC[C/G]CCATTACATGTCTGT | 83860 |
rs573942608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7851797 | TTTTTTCTTCCTTTT[C/G]TTTTCAAGACAGGGT | 83860 |
rs573946308 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893293 | ATTTAATAATCAGTT[A/G]CTAATGATGAATTAG | 83860 |
rs573991370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941925 | TTTGGAACTCTTTTT[G/T]TTTTTAATAATTATA | 83860 |
rs574004815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7844433 | CCAGGCTGGAGTGCA[A/G]TGGCGCGATCTCGGC | 83860 |
rs574009569 | in-del | -/TAAA | 0.0215492 | 0.101539 | intron-variant | TAF3 | GRCh38.p7 | 10:7935278 | AACTCTGTTTCTAAA[-/TAAA]TAAATAAATAAATAA | 83860 |
rs574018467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842701 | TTAACTTTCTCCCCA[A/G]TAAGATATATCTGTT | 83860 |
rs574031841 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958366 | ATATTCACTCAAGTC[A/G]AAAACTTTTTTACCA | 83860 |
rs574049049 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7944237 | GATAAACATACTGGA[A/G]TACTGCCAAAAATTC | 83860 |
rs574064782 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7991113 | TGTAATAATTTCAGT[C/T]GTCTCGTCTTGCCTC | 83860 |
rs574119539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7893109 | ATAGGCGTGAGCCAC[C/T]GTGCCCAGCTTCAAT | 83860 |
rs574138484 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7824155 | ATAATCAGCTTAAAC[A/C/G]TGATTCTGTGATACT | 83860 |
rs574147478 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TAF3 | GRCh38.p7 | 10:7928101 | AGAGCTCTTCCATTT[G/T]TGCCTATTTTAGATC | 83860 |
rs574150333 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011338 | CACTCACTGCAGCCT[C/G]GACCTCCTGGGCCCC | 83860 |
rs574173631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7976311 | GAGTGCAGTGGCACA[A/G]TCTCAGCTCACTGCA | 83860 |
rs574229055 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7983984 | AAATTTTCAAATGAC[C/T]TATTTTTAATGCTAG | 83860 |
rs574231248 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860700 | AACTTACTGATTTAA[A/T]CATTTTTAGTGGGTT | 83860 |
rs574269874 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911573 | CTCAGCTTTGTTTGA[C/T]AGATTTCAGTGGCTG | 83860 |
rs574275763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7915329 | TCTCACTTACAGTAT[A/G]GGTGAGGGCTTTTTA | 83860 |
rs574277628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819857 | AGACACACGCTGTAT[G/T]TCTTAGGCCCCAAGT | 83860 |
rs574280439 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827993 | CGAATATTAGTTCTC[A/G]TCCCCTTTTTCTTTT | 83860 |
rs574282364 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935620 | AAGCAAGCTAAAGCT[A/G]AGTAGAGGGCCAGAG | 83860 |
rs574288905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7864064 | GTGGTAGGTACACTG[A/G]TGAACCTGCCTTGAC | 83860 |
rs574306665 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7850782 | TAATATTTAAGAGAG[A/T]AAAGTTTAGCTTTAG | 83860 |
rs574320191 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842784 | TCCATTGGATAATTA[C/T]TATAATCAAATTAGA | 83860 |
rs574349729 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7903146 | GATCGCTTGAGCCTA[G/T]AAAGTCGAGGCTGCA | 83860 |
rs574357938 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817618 | CTTTTGAGATGTGTT[A/C]CCAATTCTGTATTTA | 83860 |
rs574382474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945015 | AGCATGAAAACATAG[C/T]ATCGGACTACATAAC | 83860 |
rs574383256 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7854870 | AACCACTGAGTGTTG[G/T]GGATGAACAGAATGA | 83860 |
rs574427195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957226 | TTAAATACCCACTGT[C/T]CTTCAAAGCTTCCCC | 83860 |
rs574445650 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:8001656 | TGTGTCCTACCCCAA[C/G]ACTAAAAACATCTAT | 83860 |
rs574449107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008933 | CACTTCATGCAGGGC[C/G]TGGAACTCAGTTCTT | 83860 |
rs574454946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895723 | TCCACTAATTGTGTG[G/T]CCTCTATCTACAGTT | 83860 |
rs574455514 | snp | A/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016102 | TTTATTTTTAATGTT[A/T]AAAAAACATCAAATT | 83860 |
rs574455665 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926818 | GCAATAGTTTTTAAA[C/T]TTTGCTGCTATTTAA | 83860 |
rs574496271 | snp | A/G | 1.66305e-05 | 0.00288357 | missense | TAF3 | GRCh38.p7 | 10:7964039 | GATGAGAATTTCCTG[A/G]GCAAGAGACCACTGG | 83860 |
rs574496998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868579 | ATCTTGGATTCACAT[A/C]CTGGAGCAGCCTGTT | 83860 |
rs574504976 | snp | C/G | 0.000114819 | 0.00757605 | intron-variant | TAF3 | GRCh38.p7 | 10:7965764 | AGTTTCTCATTTTTG[C/G]CCCTATCTGAACAGA | 83860 |
rs574517568 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877615 | TGAATAATATAAATG[A/C]TTTCCCTTTATCATT | 83860 |
rs574517669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7896272 | TACTCTTGTGACTCC[A/G]TGAATGGGGGGAAAA | 83860 |
rs574517838 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905497 | GTTCAGATGGCTGGA[A/C]ATAGCTGTGTTACAG | 83860 |
rs574536986 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7979712 | TGAAGTGAAATAGAT[G/T]ACATTTTAAATTAAA | 83860 |
rs574543054 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TAF3 | GRCh38.p7 | 10:7938545 | CTGAGAGAATTTGAA[C/T]GGCCAGTCAGACAAA | 83860 |
rs574565306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988275 | ACAACATAGCAAGAT[C/T]GTGTCTCTACAAAAT | 83860 |
rs574579032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888756 | AGTGACAGAGCTTTC[A/G]CATCTGTTCCTGGCC | 83860 |
rs574581259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7903954 | ATATTTTACGGTATT[A/G]TAGGTATCTGGAAAA | 83860 |
rs574598494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7987408 | CATGAACATTTTTCC[A/G]TGTCTGTATGACATG | 83860 |
rs574679444 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906230 | CTTATCTTTAATTTC[A/G]GTATTGGATGGTAAC | 83860 |
rs574680481 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7841878 | AAAACTTTTTATTTA[-/T]TTTTTTTTAAATAAT | 83860 |
rs574688323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7909442 | CAAATTAAAGACTTG[A/C]TTCTACCAGAAGCTT | 83860 |
rs574696590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7854236 | AATTTAGTACTGCAC[A/G]GGAATTCTGGTCAGC | 83860 |
rs574720744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7861354 | CTTGTGATCCACCCA[C/G]CTTGTCCTCCCAAAG | 83860 |
rs574739671 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7907401 | TGGGCATTTAGATTT[-/A]TTTTTTTGTATTTAA | 83860 |
rs574768077 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006332 | AGTGAGTCAAGACTG[C/T]GCCATTACACTCCAG | 83860 |
rs574770671 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978240 | CCATAAAAGTGAGAG[C/T]AGGAGCCATGAATTT | 83860 |
rs574798578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995713 | GTTTGCTACTTGATA[C/T]GTACTTGAGTTATGA | 83860 |
rs574804811 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879754 | GGTGGCTTTTAAAAT[A/C]TTGTTTTGATTTTGG | 83860 |
rs574805252 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7856020 | AGGAAGCAAGAGCAG[A/G]GTGCTATTTTAAAGG | 83860 |
rs574853945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7938211 | GTTTAAAAATCCCTA[A/G]CTTGAAGCAGTGGAG | 83860 |
rs574869238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829083 | CCATGTACCCTGACT[A/T]ATTGCAGGAAACTTA | 83860 |
rs574871409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7822267 | AAAAAAAAGGTGGCC[A/G]AAGGGGACGGGGACA | 83860 |
rs574881271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7932184 | GGTGAACATGCTACC[G/T]CTATCAGTCAGTGTG | 83860 |
rs574901344 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871465 | TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG | 83860 |
rs574903510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980524 | ATTCAAGATGACTTT[C/T]CAAGGACCTCAGATT | 83860 |
rs574905669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856416 | ACCCAGTAGGTGGAG[G/T]TTGCAGTGAGCCGAG | 83860 |
rs574930563 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827506 | AAAAAACTTGGCTGG[A/G]CGCAGTGGCTCACGC | 83860 |
rs574931260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834818 | AACAGGTAAAAAAAA[A/T]TTTTTTTGCTCATTC | 83860 |
rs574953823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7875320 | AGTCCTATAAATGAC[A/G]TTCTTTGAGCCTTTG | 83860 |
rs574994669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828092 | AATCGGTGTCAAGCT[A/G]CATTCAGTGGCACAC | 83860 |
rs574999235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952838 | TAAAAATACATACCC[A/G]CTTACACATGTTGAG | 83860 |
rs575013480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835303 | CAAAGCCGTCCTGGG[C/G]CGCATATGGCCCATG | 83860 |
rs575015413 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948513 | GGCCAGGAAAGAGTT[C/G]ATTGTAATTTCATAG | 83860 |
rs575017344 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910535 | ACAGGTGCCCGCCAT[C/G]ACGCCTGGCTAATAT | 83860 |
rs575018426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7952004 | TGAGATTAGTTTCAT[C/G]CCTACAGAACAATAC | 83860 |
rs575037346 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7835189 | GCCACACATAAAATA[A/C]ACTAACACCATCGAT | 83860 |
rs575043050 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983234 | CCCGTGAAGGACTTC[A/G]CTTCAGCAGCCCCTG | 83860 |
rs575057846 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951407 | TTTGCTCCTATGCCT[C/G]GTGCTTTGGCTGGGG | 83860 |
rs575061914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960183 | TTTAGAAATGTAATA[C/T]TAATAAGTGAATGTT | 83860 |
rs575067072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7933267 | GCTCACTGAACATAC[A/G]AGTGTTTACATGAAT | 83860 |
rs575078394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8011114 | TTGCTGTGACTACCA[A/G]CTCTGCAGACTGTGA | 83860 |
rs575099604 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7828828 | CACTTGAGGTCAGGA[G/T]TTCAAGACGAGCCTG | 83860 |
rs575138488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7945809 | CCCTTTTTCTCTCCA[A/C]ACACATTATCCCATT | 83860 |
rs575203463 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872548 | TTACTCAATGGGGAA[C/T]GTTTAAAACTCCTGG | 83860 |
rs575231782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917040 | GTTTATTCATTCAGC[A/G]AATATTCATTGAGAA | 83860 |
rs575234991 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7863376 | AGCACTTTGGGAGGT[G/T]GAGGCAGGCAGGTCA | 83860 |
rs575235422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7856524 | GAGAAAAGATTTTTT[A/T]AAAATTATAGAACCA | 83860 |
rs575241477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7960282 | AGCAGATCTGAAGTC[C/T]GCCTTGTCATTCTGA | 83860 |
rs575256932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7842089 | CGTTCATTGAGTTGC[A/G]TGAGTACCCTATTTA | 83860 |
rs575258624 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:8003666 | TAAAGAAGAACTTAC[A/C]CCATTATCCAAAAAA | 83860 |
rs575293253 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859212 | CTTGCAGTGAGCTGA[C/G]ATCATGCCATTGCAC | 83860 |
rs575299195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7857083 | TGAATATAGTTCCAA[C/T]GTGAATGTTGGTTGA | 83860 |
rs575300993 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853010 | TAGATATTAGTCCAT[A/T]TATTATCCATTGATG | 83860 |
rs575305329 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7987461 | CATCATTTATCTTGC[C/T]AGTCACCAGTTTTCA | 83860 |
rs575305510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7966409 | CAGTAAGTCAGACTT[C/G]ATTTCATAGCATACA | 83860 |
rs575307284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7996577 | ATCACTGATCCAGAT[A/G]TGAGGTTTTATAGTA | 83860 |
rs575338091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7889635 | TCCAGACTCATATTC[A/C]GTGGCTTACTGGGCA | 83860 |
rs575341851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7930236 | CCTAAGAGAAATCCT[A/G]AAAGGCCAGCAGTTA | 83860 |
rs575369612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7995844 | AATGTTAAAATTTGA[G/T]CTGTGAGGATCAAGA | 83860 |
rs575381752 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | TAF3 | GRCh38.p7 | 10:7902393 | GCACCACTGCACTCT[A/T]GCCTGGGCAACAAGA | 83860 |
rs575400128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883139 | CCAGTGATACCCTCC[A/G]TAGCAAAAGGAAAGG | 83860 |
rs575409161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7835849 | TTGTCACCTGCATGT[A/G]TTTTGGCACTGATGG | 83860 |
rs575412597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7829157 | CTTTTAGAGTTTCTA[C/T]TTTTTAAAATTTAAA | 83860 |
rs575415568 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845259 | AAAAAAAAATCTCCC[A/G]CTGGAATATAACTGC | 83860 |
rs575417730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7980590 | TTCCCTGTAGTCTAT[A/G]TTGAAGATAAAACCA | 83860 |
rs575475111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7847153 | GGAATTGGCCATATA[A/C]GTGAAATTTCAGACT | 83860 |
rs575481092 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012339 | TGGAAATGCCACTTA[A/C]ATTCCCTTAGCTCCG | 83860 |
rs575483867 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958794 | ATCATTTCTAATTTT[A/G]AAAATTGTTTAAGTA | 83860 |
rs575498647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7903872 | TACAGTCTCTCGGGG[G/T]ACATAAGGGACATAA | 83860 |
rs575505420 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7989272 | GTAGGATAAAGCCCA[C/T]TCAGGCCACATGGAC | 83860 |
rs575529567 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955603 | CAATTTCCCTTTATT[A/T]CCTAATGTCTATGAA | 83860 |
rs575536637 | in-del | -/GGTGGGC | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7842000 | TTAAATCAGGTGGAT[-/GGTGGGC]TTTTACCAAATGACT | 83860 |
rs575539675 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TAF3 | GRCh38.p7 | 10:7966216 | GTTTTCTTTTTGGTG[C/T]GCCATTTTGGCATGT | 83860 |
rs575541669 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980480 | AGGAGTCAATGGTGA[A/G]TCCAGGACCTCCTCC | 83860 |
rs575542056 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954313 | TGAGATTCAGAGTGC[A/C]CTCCATAGGCGAATG | 83860 |
rs575570669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7862895 | TTATTGTTGAGTATT[G/T]TTCCATTACGTGTAT | 83860 |
rs575588109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898113 | ACCCTTCTGTATCAA[C/T]TGGTATGCTTTCAAC | 83860 |
rs575598294 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816925 | GCTGGAAAAAAAATA[A/C]CTGCGTGCATATATA | 83860 |
rs575635533 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003945 | TGGAAAATATAGTTA[C/T]TTTCATAAAAAAAAA | 83860 |
rs575635884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7865600 | GGCGTAGTAACAGGC[C/T]TGCGTGTCGCTGGCT | 83860 |
rs575636690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7855903 | GCCTGGCCAATATAG[C/T]GAGACCCCATTCTCC | 83860 |
rs575690089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7904720 | TGTAGTGTGCACAGC[A/G]TTGGCTTTCATGATA | 83860 |
rs575694155 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917644 | TGGAGAATAGGTCGG[A/G]TTCTGAGGCCGTCAC | 83860 |
rs575696105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011776 | AGTTTGTGTTAAACT[G/T]GGTAATCTCTGTGGC | 83860 |
rs575698897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875947 | ACTCCAAACAAGTGA[C/T]AGTAATCTTATATTA | 83860 |
rs575699036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7898920 | AGTGAAAGTTTCATG[C/T]GTACTGTCAGGGATG | 83860 |
rs575699554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860441 | CTTCTTTCCTCCAAA[A/G]GTAACCCCTACACTT | 83860 |
rs575719761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850006 | TTTTGATGTTAAAAA[A/G]TAGGGAATATTATTT | 83860 |
rs575739415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7917224 | GTGCTGTGAGAAGAA[A/G]CAAGGAGGGAAAAGA | 83860 |
rs575742372 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002186 | AACTCCATTAACCAA[C/G]AACTGAAAACGCCTG | 83860 |
rs575758283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8011280 | TTTTCTTTTGAGGTA[A/G]TCTCACTCTTCTTGT | 83860 |
rs575774175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7868135 | CCACATATAAGGGGG[C/T]ATGTGTAGTTCAAAG | 83860 |
rs575777707 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930148 | AGACTGCAGTGAACC[A/G]TGATTGTGGTACTGC | 83860 |
rs575813657 | in-del | -/GC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858827 | TGTGTGTGTGTGTGT[-/GC]GCGCGCGCCTGCATG | 83860 |
rs575818588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7947283 | CCCCTCCAGCCCCCA[C/T]CGCAGGCCGGATAGT | 83860 |
rs575818871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7876526 | GGAGTTCCTGTAATG[C/T]TGTTTTTGGAAATGA | 83860 |
rs575832680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7946494 | ATTGGGAGGCCGAGG[C/T]AGGCAGATTATTTGA | 83860 |
rs575851536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7998765 | AATTGCTTGAACCCA[C/G]GAGGTGGAGGTTGCA | 83860 |
rs575867389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7997799 | GAGAAAAAGGGATAC[C/T]TCAGAGAGAAAAATA | 83860 |
rs575868435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7883629 | TAATTATTCCTAATA[G/T]TTGCTGGATGGTAAA | 83860 |
rs575869866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7868743 | CTAGTGCCATGTCTT[C/T]TGGCACCTAGAAAGT | 83860 |
rs575870423 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948258 | TCTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTA | 83860 |
rs575873105 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874685 | GGACTCTAACAGATA[C/T]GTTTTGTCTTAGTTT | 83860 |
rs575905246 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889624 | CTTTTGTGAGGTCCA[C/G]ACTCATATTCAGTGG | 83860 |
rs575914269 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:8005293 | TCATAGATTTGATTA[A/T]CTTTGATTATGTGCT | 83860 |
rs575972000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7865233 | AGCACTCTGGGAGGC[A/C]GAGGCGGGCGGATCA | 83860 |
rs576017091 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920861 | ATTTTTTTAACAGTG[A/G]TTTATACTGTAGCTA | 83860 |
rs576037621 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819609 | GTCTGGTAATATCTA[C/T]AGCTAGTGGTATTTA | 83860 |
rs576051733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852767 | AATTCTGTTTTCTTC[A/G]CAAGCTGGAGTGCTT | 83860 |
rs576140018 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950332 | CAGAATATGTGGGCA[C/T]GAAGACCCTGTGGAG | 83860 |
rs576152389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7908135 | TGCCTTCTCCATTGC[C/T]ATTTCCTCTTGTGTG | 83860 |
rs576163763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832407 | GAATAATAATACTTT[A/T]TAATTTTTATGGGTA | 83860 |
rs576178199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7920231 | TGCACTCCGGCCTGC[A/G]CGACAAAATTTATTT | 83860 |
rs576181376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7879868 | AGTATTCAAATTCCA[A/C]GTATGTATTTTATTT | 83860 |
rs576199743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:8001492 | TGTTTATATAAGAAG[A/G]CGTAATGCTTTATTG | 83860 |
rs576200946 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947681 | AGCATCGAAGATGCC[A/G]GCATGGCTTGATGAA | 83860 |
rs576202056 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016933 | GGGGCTGGAGAGCTC[A/G]AGGGATTAGTAATGG | 83860 |
rs576208769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7871502 | AGGCTAGAGTGCAAT[A/G]GTGTGATCTCTGCTC | 83860 |
rs576213519 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971521 | AAAACCTTGGACAGA[C/T]TATATTGACAAAGCT | 83860 |
rs576214041 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900074 | TATATTGAAAAGATA[C/T]CCATCCTGTGTAATG | 83860 |
rs576242448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872085 | TATATTAAAGAAAGT[C/G]AGCGAAATTTCCATA | 83860 |
rs576244426 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TAF3 | GRCh38.p7 | 10:7956372 | CGTGCCTATAATCCC[A/G]GCTACTCGGGAGGCT | 83860 |
rs576260835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008245 | GGAATTACAGGTGCA[C/T]GCCACTGCACCCGGC | 83860 |
rs576261830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7943435 | ATAGTAGGTGTACAA[C/G]ATACACTTGCTGAGT | 83860 |
rs576264514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7887481 | CTCTTCTCTCTTTTT[A/C]TCTGTTTCTTTTCTT | 83860 |
rs576266007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7886812 | CCTTATTCAGGAAGC[A/G]AAACTTATGCTTACA | 83860 |
rs576273579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7949294 | AGCCGGAAATAAAGA[A/G]TGGGCTGCTTAGCAC | 83860 |
rs576275236 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924040 | CAGTATTTAGGCCAT[A/C]CTTTCATTAAGATAA | 83860 |
rs576327199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7880659 | GCTACTCTACACAGT[A/G]CATGTTGTATCTTTC | 83860 |
rs576354135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978868 | ATACCCTTTAGAGGA[A/G]TAAGATTTGTTAAAA | 83860 |
rs576383019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7957127 | TAGCACAAGCGGAAA[A/C]GGTGACATCACTTTT | 83860 |
rs576418092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7929593 | ATAGACAAACTCCTG[A/G]ACTCAAGTGACCTAC | 83860 |
rs576435654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7866364 | CACAAGAGAATGAAC[A/G]TAGGGGCCTGTGATG | 83860 |
rs576437914 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7923937 | TTTGGAAATAAAGGA[A/G]TATTCCAAGGTATAA | 83860 |
rs576449140 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7956465 | GCACTCCAGCCTGGG[A/C]AACAGAGTGAGACTC | 83860 |
rs576461935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7820380 | GGCACCTGAGAAATA[C/T]TTGTTGAATAAATGA | 83860 |
rs576482824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827905 | AGGCTGCAGTGAGCT[A/G]TGATCACACCACAGC | 83860 |
rs576501976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7854183 | TAAGAAGTAAGAACC[A/G]TCAGGTTTACAGGGA | 83860 |
rs576539969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7937336 | TCACTCTGCATTCTT[C/T]CCAGGATTTGGTGTT | 83860 |
rs576559914 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7891037 | TTGAATTGGGGCCCC[C/G]CCCTTTGCATGTCTG | 83860 |
rs576592777 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7993345 | ACTACACCCAGCTAA[-/T]TTTTTTTATTTTTTG | 83860 |
rs576604859 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856332 | AATACAAAAATTAGC[C/G]AGGAGTGGTGGTGCG | 83860 |
rs576606813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7833615 | CCCAAGAGGGCTTCA[A/G]TTTTTCTTTTCAACA | 83860 |
rs576606895 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832714 | ACCACCACACCCGGC[A/T]AATTTTTGTGTTTTT | 83860 |
rs576608580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7825806 | CCGCTATGAACATCG[A/G]TGTGCAAATCTCTGT | 83860 |
rs576611769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7895538 | TGCCACATCTATGCT[A/G]CTGAGTTGTCAGTAA | 83860 |
rs576634938 | snp | A/C/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846179 | AGCCAGGACGGTCTC[A/C/G/T]ATCTCCTGACCTCGT | 83860 |
rs576647148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7971769 | CTGGAAAAATGGAGA[A/G]TTAGAGCTTTATCAG | 83860 |
rs576666896 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853177 | TTAAAAAAATCATAT[A/G]AACTTATAATTAAAT | 83860 |
rs576669331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7826373 | CATATTTAAATACTA[C/G]CAAGGAAATGTAACT | 83860 |
rs576680445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7969000 | TTAAAATAGAACCAC[A/G]TTAACTTTTTATAAA | 83860 |
rs576696077 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7970826 | GAGAATGATAAATCA[G/T]CTAATTGGTTTGTAC | 83860 |
rs576716086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7950630 | ATATCCATGTAGTTA[C/T]ATACAGTTATCCTCA | 83860 |
rs576717027 | snp | A/G | 3.3253e-05 | 0.00407742 | missense | TAF3 | GRCh38.p7 | 10:7964715 | GAGCCTGTGCTGAGC[A/G]AGAGCCAGATCCTTT | 83860 |
rs576760260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839490 | GAGGAGCAGTCGCAA[A/T]AATTAGCTTGTCCAA | 83860 |
rs576784902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860904 | TCCTGGGTTCAAGCA[A/C]TTCTCTGCTTCAGCC | 83860 |
rs576788983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7963757 | GGCACATGTATACCT[A/G]TGTAACAAACCTGCA | 83860 |
rs576822302 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7833753 | GGTGACTTGAGCTTT[C/G]TCCTTCTCATAGACA | 83860 |
rs576843091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875711 | TATATCTAGTTTAGT[A/G]AATTTACCCCCCAAA | 83860 |
rs576893616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008823 | TCATATTTCTGTGAA[C/G]AATGCATGTGTATTG | 83860 |
rs576913056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7962832 | AACTGTGAGCTCTTT[C/T]AGTTGTGATTTATTT | 83860 |
rs576933292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944824 | CAATTAATCAAGAAA[C/T]TCATATTTTGGGACA | 83860 |
rs576951617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7978964 | GAAGATCACTTGAGG[A/C]CAGGAGTTCAAGGCT | 83860 |
rs576958730 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016438 | CCTCGTTGTTCAAGA[A/G]GCCAGAATTTTTCTA | 83860 |
rs576959799 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7987359 | TTATCTTACACATAC[C/T]GTTCAGCAGCTTATC | 83860 |
rs576960512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8008324 | GGCTGGTCTTGAACT[C/G]TCGACCTCAGGTAAT | 83860 |
rs576966905 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7995678 | TTCAAATAGGTCATG[C/T]CTGCATTAAAAGATA | 83860 |
rs576991615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7944031 | GGAAGAATGCAAAAC[C/T]ATGAATCCATTCATG | 83860 |
rs577001059 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924504 | AACAAACATCAAAGT[C/T]AAGTGTGTAGGTCAT | 83860 |
rs577020510 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | TAF3 | GRCh38.p7 | 10:7908564 | CGTCCCCACCCTCAT[-/A]ACCCACCTCCTCTTC | 83860 |
rs577037286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7875336 | TTCTTTGAGCCTTTG[G/T]CTTATTAATCTTTAT | 83860 |
rs577062975 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004224 | CCCAGCTAATTTTTG[G/T]ATTTTTAATAGAAAT | 83860 |
rs577065186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7872156 | TTTTTTTAACCTGCA[A/G]AGTTTCCAGTTTACC | 83860 |
rs577076251 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903868 | GGCTTACAGTCTCTC[A/G]GGGGACATAAGGGAC | 83860 |
rs577079747 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7847123 | ATAGCATTTCTGGCT[C/G]ATGAGGATTATAATG | 83860 |
rs577082042 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874879 | AAATTATGTATTGAG[C/T]TCGGGTTTTTTTCCT | 83860 |
rs577082131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7915244 | GCCACTGCGCCTGGC[C/T]GCTCCCCAGCCTTTT | 83860 |
rs577111891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7860493 | TATTATTTTATGAGT[G/T]TATTTGTACATTTTA | 83860 |
rs577112842 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7882123 | TTATAAATTGTACTG[A/T]ATTATGGGAAAACAA | 83860 |
rs577125449 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7872916 | TTTGGGGGCAGGGAG[G/T]TTAGAGAGAATCCAA | 83860 |
rs577155902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7916189 | CTTGCTTTCAGTGAG[C/T]TAGACAGTTTCCTTT | 83860 |
rs577159110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7972691 | ACTTAATTTTTACAT[A/G]TTGTATTATTTAGGG | 83860 |
rs577218785 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869244 | TCCTTCCTGACTTCT[A/G]CCGTGTGTGTGTGTG | 83860 |
rs577231858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7878755 | TGTATATGAGACAGA[A/G]TCTTGCTCTGTTGCT | 83860 |
rs577234778 | snp | A/C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906863 | GCTGGGACTGCAGGC[A/C/G]TGCACCACCATGCCC | 83860 |
rs577252814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7867829 | AACTTTTGACTCCCC[C/G]AAAACTTTACTAATA | 83860 |
rs577271194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7912827 | TGGCGAGGCACTGGT[A/G]CTTTTTTTCCTTTCT | 83860 |
rs577273463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7988276 | CAACATAGCAAGATC[A/G]TGTCTCTACAAAATA | 83860 |
rs577282698 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TAF3 | GRCh38.p7 | 10:7910479 | TCCACCTCCCAGATT[C/G]AAGTGATTCTCCTGC | 83860 |
rs577282904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7893812 | TTTCTTATCTTTATT[A/G]GGATCCTTCTTACAT | 83860 |
rs577292165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7827979 | AAAACACATGACAGC[A/G]AATATTAGTTCTCGT | 83860 |
rs577293009 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839105 | ATGTTAGTTACTTGC[C/T]CCTCGTTGCTTCGTG | 83860 |
rs577298142 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7924745 | CCCCAACAGAACACT[A/C]TCTGTGTTTTTTTTT | 83860 |
rs577336000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7896170 | TGTTCTATTGTGTAT[A/G]CTAGTAAGGTAAAAA | 83860 |
rs577347931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7931360 | CTAACCACTATGCCA[C/T]ATTTATTTTCCTGCT | 83860 |
rs577349655 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846227 | CTCCCGAAGTGCTGG[C/G]ATTACAGGCATGAGC | 83860 |
rs577350967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7982274 | AGTCGGAAATAGAAA[C/T]AGATCTTCTTCCCTA | 83860 |
rs577353732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7828749 | GCATAAGAAAGAAAT[A/G]TAGGCTGGGCGCAGT | 83860 |
rs577379928 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002125 | TTGATCACAACTCTC[A/T]TCTTCCTATCATCCT | 83860 |
rs577397671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7888638 | TACAGGTTATGTAAG[C/T]GCCCTCACCAAATGG | 83860 |
rs577403026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7850598 | TGAGAATTGCTTGAA[A/C]CCAGGAGGCAGAGGT | 83860 |
rs577414138 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906151 | TTCATCTCTTGTCCA[A/G]TTCCTCTTTCTCCTC | 83860 |
rs577424532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7834330 | AGCAGTTTTGTAGTT[G/T]CAAGTCTTACATTTA | 83860 |
rs577441040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7884660 | CCAAAAGTGCTGGGA[C/T]TACAGGCGTGCGCCG | 83860 |
rs577445727 | snp | A/C | 1.73821e-05 | 0.00294801 | missense | TAF3 | GRCh38.p7 | 10:7965622 | AGAAAAGAAAAAGGA[A/C]AAAAAGGAGAAGAAG | 83860 |
rs577468958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7951855 | CCACATAGCCCAATA[A/G]TTGGCAGAGGCACAT | 83860 |
rs577476958 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7947935 | TAACTGAAATCACCC[A/G]TGTACAGACAGGAAA | 83860 |
rs577505261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7877628 | TGCTTTCCCTTTATC[A/G]TTATCTTGTAGTAAG | 83860 |
rs577520174 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828747 | TTGCATAAGAAAGAA[A/C]TATAGGCTGGGCGCA | 83860 |
rs577523538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8012873 | CCTTACAAAATAAAC[C/T]GGATGCAATAATGTG | 83860 |
rs577528091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7942311 | CTTAGGGTAAATATT[C/T]TATCAAACATATTTT | 83860 |
rs577542177 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847467 | TTCTTTTTTTTAAGA[C/T]AGAGTCTTGCCCTGT | 83860 |
rs577555647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7919189 | TTGGATGTCCTAGGA[A/G]GCCTAGCTTCTGGCT | 83860 |
rs577579200 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TAF3 | GRCh38.p7 | 10:7935542 | TGAGCCGAGATCGCG[C/T]CACTGCACTCCAGCC | 83860 |
rs577580166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7870465 | TTATTTACGTGAGTG[A/T]TGCCTGATGGAAGAT | 83860 |
rs577581768 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826316 | TATTTTTATAGCATG[C/G]AAATATTCCATAATA | 83860 |
rs577618601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7919836 | TACGGAGGGCTGACT[A/G]TGTATGCTTAATGAC | 83860 |
rs577641572 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7961914 | GAGTGCAGTGGCGCA[A/G]TCATGGCTCATTGCA | 83860 |
rs577664920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7941357 | AATTTCAAGAAAGAG[A/G]AAAAGTGATCAGCAG | 83860 |
rs577673442 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7937738 | AATAGTCACAGCACC[C/T]AACATTTCAAGAGCA | 83860 |
rs577691007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7831388 | TCTCACTCCATCGCC[A/G]AGGCTGGAGTGCAGT | 83860 |
rs577730945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7899439 | CTCCTCCATGATTCT[G/T]TCCTGAGGAGCAGTT | 83860 |
rs577731658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7832986 | GGATGATTTGAGGCC[A/G]GGAGTTCGAGATAAA | 83860 |
rs577749090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7934706 | TGTCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 83860 |
rs577755050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7832047 | TTTTGTGGAGAGAAC[A/G]TTTAAAACTTACTCT | 83860 |
rs577790784 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842316 | AGACATGCACCACCA[C/T]ACTCAACTAATTTTT | 83860 |
rs577792528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7906842 | CCTGCCTTGGCCTCC[C/T]GAGAAGCTGGGACTG | 83860 |
rs577795022 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866240 | CACTCTTCCAGGCAC[A/G]GGGGATGGAGCAGTC | 83860 |
rs577812639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7934291 | AAAAATGCATTGTCA[A/G]AATTTAATTGGCAGG | 83860 |
rs577815383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TAF3 | GRCh38.p7 | 10:7843356 | TCAAGCGATCCTCCC[C/T]ACTCAGCCTCCTAAA | 83860 |
rs577823626 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817116 | AAACACCCAGGGTGG[C/T]GGCGGTAGCGGGACA | 83860 |
rs577839785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7968469 | TGGAATCCAGCAGAC[C/G]TGGAATAAGATCCAG | 83860 |
rs577854353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7936389 | TTCTCTTACAGTTTA[A/G]AGCATTATACGATTA | 83860 |
rs577854466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7928723 | ACGATGATCTAGGTA[A/G]TGGCCTAAGACTGGG | 83860 |
rs577854516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7900105 | GTGTAAAGCTTACAC[C/T]GAATGGTATAAAATC | 83860 |
rs577861869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7858092 | GTTTTGTTACAAATA[G/T]GGACATGAAATCATA | 83860 |
rs577865844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954857 | GAGATTCAGAGTGCA[C/T]TCCATAGGTGAATGA | 83860 |
rs577872333 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968467 | TTTGGAATCCAGCAG[A/T]CCTGGAATAAGATCC | 83860 |
rs577911803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7967847 | ATATGGGCAGGTCAG[C/T]TATTAATAGGTTTTA | 83860 |
rs577929177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7954490 | CCCAGTTAACACAGA[A/G]CTCTCCATAGTGAGA | 83860 |
rs577929295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961945 | GCCTCAACCTTCTGG[A/G]CTCAGGTGACCCTTG | 83860 |
rs577936046 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924496 | CAAATAATAACAAAC[A/G]TCAAAGTCAAGTGTG | 83860 |
rs577954144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7992787 | ATTAATATTTTCAAA[C/G]ATAAAAGAGTAAAAT | 83860 |
rs577976445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7949190 | CTCACCATCACAGAG[A/C]AAGAGGAAGGGGCTG | 83860 |
rs577979436 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7886865 | CTAATCTTGAATTGG[A/C]AAAATTTTAAATACC | 83860 |
rs577982773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7961548 | AGTTCTTCTTCCTTT[G/T]CTTTTTATATATAGG | 83860 |
rs577995984 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992361 | CATAATGTAACCATG[C/T]CAAAGGTAGTAGACT | 83860 |
rs578013280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7837599 | AGTGATCTGAGATTG[C/T]ACCAGTGTACTCCAG | 83860 |
rs578013374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7830796 | ACCATGTCATTTACC[G/T]TTTAGTTTGTGACTC | 83860 |
rs578016954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7991997 | AAAATAAAAAGTAAA[G/T]GTGTATCTTTTATGG | 83860 |
rs578041516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7948759 | TTCCCTATCAAATTT[A/G]TCACTGGGTACTGAA | 83860 |
rs578061202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7839344 | GCTTTCTCTTTAAGT[A/C]CTACACTCATTCTCC | 83860 |
rs578067355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7921251 | AGCAGTTTTATTTGG[C/T]AGTTTTTCTATCCTT | 83860 |
rs578067983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7984163 | TCCAGAAAAGGAGTT[C/T]TTGACTTCCTTATAT | 83860 |
rs578127201 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TAF3 | GRCh38.p7 | 10:7969340 | ATTATCCAATTGCAG[C/T]CACAGCCATAATAGT | 83860 |
rs578152507 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TAF3 | GRCh38.p7 | 10:7960878 | AGGCATAACTCTTCC[A/G]TGTAATAAAGAACAG | 83860 |
rs578204503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:8009688 | ATGCGGTGGTGAGAT[A/C]TCAGCTCACTGCAAC | 83860 |
rs578220795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7977788 | AGAAATGCCAAAGGC[A/T]TGGAGAGACAGTATG | 83860 |
rs578224554 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TAF3 | GRCh38.p7 | 10:7858803 | ACTGGTACATTATAG[G/T]CTCTGTGTGTGTGTG | 83860 |
rs578237829 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TAF3 | GRCh38.p7 | 10:7949219 | TGGTTCTGTAAATCA[-/G]AGTCCACTTGCCCTT | 83860 |
rs578242643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TAF3 | GRCh38.p7 | 10:7985932 | GGGACTATGGGCACC[C/T]GCCCCCACACCCAGC | 83860 |
rs578243265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7851871 | CTTGCTGCAGCCTCA[A/G]ACTCCCAGGCTTTAA | 83860 |
rs578253731 | in-del | -/C/T | 0.0879971 | 0.190408 | intron-variant | TAF3 | GRCh38.p7 | 10:7936511 | TCTTTTTTTTTTTTT[-/C/T]CTTAATAGACTTTAT | 83860 |
rs578256771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7852489 | CCTGTAGAGTTTTTT[A/G]TAGTCTGAATTTTGC | 83860 |
rs745311818 | snp | C/G | 1.76537e-05 | 0.00297095 | missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818732 | AGAGTTACTCCAGGT[C/G]GTTGTTGAGGGTCTC | 83860 |
rs745320114 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987272 | AGTGAGTCGTGATCA[C/T]GCCACTGCACACCAG | 83860 |
rs745320684 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834884 | GTGTATCTTGTCAGA[C/T]CATATAGCTACTGTC | 83860 |
rs745332276 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995052 | TTTGAGTTATTCAAC[A/G]AGAATTATATAAAAT | 83860 |
rs745336002 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941702 | AAATAGTAAGTTCTC[A/T]TGGGGTCAGTAAATA | 83860 |
rs745352840 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835609 | TCCTGGGCTCAACTT[C/G]TAGCCCCATTGGATC | 83860 |
rs745363806 | in-del | AAACAAAAAAAAAA/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881249 | TGTCTCAAAAAAAAA[AAACAAAAAAAAAA/C]CCCACAAGCTCTTTT | 83860 |
rs745381604 | in-del | -/CTCC/CTCCCC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957798 | TCTCTAGCGCGCTCT[-/CTCC/CTCCCC]CTCTCTCTCTCTCTC | 83860 |
rs745389298 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942679 | ACAGATCCCAAGAAG[C/T]GCTGGGGAATGTGGT | 83860 |
rs745402835 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930408 | TTAGTATATAGACTC[A/G]TACAGCCCTATTTCT | 83860 |
rs745430142 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956891 | AAGATTTTTTTGAAA[A/T]TAGGTATTACCACAC | 83860 |
rs745441238 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931673 | CATGTTATGTTTTCA[A/C]ATCTCATTGTATGTT | 83860 |
rs745443964 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930376 | TTATTAGTGAGTAAT[A/G]CTAAATGTCAGACCA | 83860 |
rs745461039 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917917 | TCTGACTGGAGAAGA[C/T]CGAGGAGAGGAGTGG | 83860 |
rs745472333 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846368 | TATTCTGTCCTTTCA[C/T]TTAAAATAATGTTTC | 83860 |
rs745512027 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966647 | TGCCCTCTAAAAGTT[A/T]TCTTCTTTGAGCTTG | 83860 |
rs745512927 | snp | A/G | 1.68508e-05 | 0.0029026 | missense | TAF3 | GRCh38.p7 | 10:7964567 | CTCAGTGAAAAAATC[A/G]GTAAAGAGACTATCC | 83860 |
rs745524256 | in-del | -/TTTGATAAAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997342 | GATAATTTGGATTAC[-/TTTGATAAAT]TGGTTTCATCGTGTT | 83860 |
rs745532570 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910152 | GCACAGCCTGTAGGT[A/G]GGGTACAGAGGCCAG | 83860 |
rs745538085 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859213 | TTGCAGTGAGCTGAG[A/C]TCATGCCATTGCACT | 83860 |
rs745539384 | snp | A/G | 3.81847e-05 | 0.00436931 | intron-variant | TAF3 | GRCh38.p7 | 10:8009359 | GCCCGCGCGGTTAGC[A/G]TGGAGACGTTTTCAG | 83860 |
rs745563021 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974755 | AGAAGTTAAGAAAAT[A/G]TTTAAGATGGAGTGG | 83860 |
rs745567839 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891150 | GGCTGCAGGTTTTTG[-/A]TATAGGTTATCTCCC | 83860 |
rs745597656 | snp | A/C | 3.31598e-05 | 0.00407171 | missense | TAF3 | GRCh38.p7 | 10:7964211 | CTCCAGTCCATGTAC[A/C]GGACAGTACAGACTT | 83860 |
rs745616341 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872407 | TCTGTGTTCGTGTAT[A/G]GCCAATGCCAGAACT | 83860 |
rs745630146 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897762 | ACTCCTGGGCTCAAG[C/T]GAGCCTCCTGCCTCA | 83860 |
rs745653199 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966284 | ATCTTTTATTCCTTC[C/G]GTTTTCTGCTTTAAT | 83860 |
rs745658422 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952238 | TATTGACATTGTCTG[A/G]AGAGATCTACTTGTA | 83860 |
rs745707245 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977393 | CTCTTTCCTAAGGGA[A/C]TTAGAATTCCACAAG | 83860 |
rs745708279 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892971 | ATTATAGGCATGCAC[C/T]ACCACACCCCATTAA | 83860 |
rs745710710 | in-del | -/ATAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863673 | TATATATATACACAC[-/ATAT]ATATATATACACACA | 83860 |
rs745717625 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837723 | GTAAGTACTCAGAGG[C/G]TGAGGTAGGGGGATC | 83860 |
rs745731705 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879378 | ATACTCATGCATAAT[A/T]GATTATATATTTTAT | 83860 |
rs745732556 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916641 | AAAAATAAAGTGTAT[A/G]TATATATATTTAATT | 83860 |
rs745733489 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874339 | TAGTAGACAGCATTT[A/G]TAAATTACAAATATT | 83860 |
rs745743343 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826483 | TGATACTGACTTCTG[G/T]CTGAAATTACTATAT | 83860 |
rs745747619 | snp | C/T | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964068 | GGATAGTCCTGAAGC[C/T]GAAGAACTGCCAGCC | 83860 |
rs745759452 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880444 | TGAGAAATAAGAAAT[A/G]TGCAGCTATCCTGAC | 83860 |
rs745765773 | snp | A/G | 1.70598e-05 | 0.00292055 | missense | TAF3 | GRCh38.p7 | 10:7965209 | AAAGAGAAAGACAAG[A/G]AAACTGGCAGGGAAA | 83860 |
rs745770665 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012833 | TCTAGTCAGTGTGGT[A/G]TTTGAAAGTCTGGGA | 83860 |
rs745778134 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842164 | TTGTTTTTTTTTTTT[-/GT]TTTTTTTTTTGTTTT | 83860 |
rs745786023 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841853 | TTATAGTCTGCAGGC[A/T]ATCCTCTAACAAAAC | 83860 |
rs745786239 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999810 | AGGAGGTTTTCTCTT[C/G]CCCCTCCTTTGACCC | 83860 |
rs745795693 | snp | C/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014999 | CTGGGGGCTGCCCCT[C/T]CTCCACTTCTCTAAT | 83860 |
rs745809339 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820932 | GTCCTTGAGTATACC[A/G]TTAGTGATAGGCTAG | 83860 |
rs745812732 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896129 | GGCCTCAGTTTACCA[A/G]GCCCTGAAATGAAAT | 83860 |
rs745839154 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985947 | CGCCCCCACACCCAG[C/T]TAATTTTTGTATTTT | 83860 |
rs745858533 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952969 | TACTAGAAGATATAA[C/T]GATGAAGTGGATTAT | 83860 |
rs745865346 | snp | G/T | 1.65842e-05 | 0.00287955 | missense | TAF3 | GRCh38.p7 | 10:7964115 | TATTAAGCACTAAAG[G/T]GGACACGCTAGATGT | 83860 |
rs745907554 | snp | A/G | 3.32226e-05 | 0.00407556 | missense | TAF3 | GRCh38.p7 | 10:7964802 | TTTCAGGCCCGGAGT[A/G]TACTACTCCCAAAGC | 83860 |
rs745910676 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938787 | CTGCCGAATGTTAAG[C/T]GTTGAAAGAGACTGC | 83860 |
rs745912195 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937481 | CTATTTGCCATCTGT[A/G]TATGTCTTTGGTAAA | 83860 |
rs745921530 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963629 | CATGGACACAGAGGG[-/A]AGGGGAACATCACAC | 83860 |
rs745973632 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927159 | TGAGTTAATGTTATA[C/T]ACTCATCTTTCATGT | 83860 |
rs745977324 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912876 | CCTTATGCTGGTTAC[C/T]TTCACCTGTTAGGTT | 83860 |
rs745986005 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962244 | TATCCTCAGAATATC[C/T]TTCACCTCTGCTGCT | 83860 |
rs746032384 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914154 | TAAGATTGTCATTAA[C/T]TTGCTAGGTGTGATG | 83860 |
rs746042266 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830899 | ACAGTTGGATGTTGC[A/G]CATTGTGCACTCATA | 83860 |
rs746085657 | snp | A/G | 3.59247e-05 | 0.00423805 | missense | TAF3 | GRCh38.p7 | 10:8009106 | GTGGTCCCTGCCCCC[A/G]AGGCCAAGCCGGCGC | 83860 |
rs746098874 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003696 | ATCTTTTAAAATACT[C/T]CTCCCTTCTCTAGTT | 83860 |
rs746102667 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992196 | TGCAGAGCAGCAAAA[-/G]CCTTTCTGAAATCAC | 83860 |
rs746106549 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915131 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 83860 |
rs746108981 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871263 | CAAAGGAAATATTAG[C/T]AATGATGGCTATTTC | 83860 |
rs746116636 | in-del | -/GGGG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897261 | TTAAGCCAGGTCGCC[-/GGGG]GGGGGGTCACTTTTA | 83860 |
rs746144869 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944252 | ATACTGCCAAAAATT[C/G]AGGTGGCTGAATGCT | 83860 |
rs746146638 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990578 | TGTGCTCTACTGTTA[C/T]TATATAGTTTTAAAG | 83860 |
rs746165727 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994551 | ATGAGGTCTCACTGT[C/G]TTGCCCAGGCTGGTC | 83860 |
rs746168122 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841298 | CTGTGGAGAGCCTGC[-/TG]TGTCTGCAGGCTCAC | 83860 |
rs746172251 | snp | A/G | 1.69278e-05 | 0.00290923 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965598 | GGAGAAAGAGAAGGT[A/G]AAGGAGAAAGAAAAG | 83860 |
rs746176117 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010757 | ACTAAAAATACAAAC[A/G]AAATTAGCTGGGCAT | 83860 |
rs746176451 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947934 | CTAACTGAAATCACC[C/T]ATGTACAGACAGGAA | 83860 |
rs746187845 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962093 | TGGGCTCAGGTAATC[C/G]TACTCCCTCGGCCTC | 83860 |
rs746213784 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924713 | ATTGAAAAAGAAAAA[C/T]GCTCATAATCTCACC | 83860 |
rs746251463 | in-del | -/AGCG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957789 | TCTCACGCTCTCTCT[-/AGCG]CGCTCTCTCTCTCTC | 83860 |
rs746253326 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827372 | ACAGTGTTTAACATA[C/T]AAAATACATAACAGT | 83860 |
rs746273668 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906751 | ATTCTACCAATAGGC[A/G]CCTTATGCCTTTATT | 83860 |
rs746299340 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876587 | GAGGCAGTCTTACCT[A/G]TTCCTGTAGGTGAGC | 83860 |
rs746326722 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894484 | GTAGTGTGATGCGTC[A/G]GTGACCTGATCGATT | 83860 |
rs746328033 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824024 | TCAGGTGCTGTTCCA[G/T]ATGCTTTTGATCATC | 83860 |
rs746355049 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853784 | GTATATCCCAAAAGC[C/T]TAAAATAGTTACCAT | 83860 |
rs746356322 | snp | A/G | 1.66059e-05 | 0.00288144 | missense | TAF3 | GRCh38.p7 | 10:7964885 | TCCGGTGGAACCTCA[A/G]GTTCCGATAACTCAT | 83860 |
rs746362395 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995832 | TATAATTATATGAAT[A/G]TTAAAATTTGAGCTG | 83860 |
rs746376087 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895806 | TAGGGGTGAAGTGAA[C/G]ATAAAGTGAGAAAAT | 83860 |
rs746391547 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882658 | TGTCTAAAGGTGGAG[G/T]GCTCCTATCAGAAGG | 83860 |
rs746402566 | snp | A/G | | | missense | TAF3 | GRCh38.p7 | 10:8014743 | AAGAGGAAGCATCGA[A/G]CCCACTGACGACTCC | 83860 |
rs746411872 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903239 | AAAATGTAATAATCC[A/G]TTTCTGTCATCATGT | 83860 |
rs746429994 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982938 | CTTCATCTCTAGTGG[A/T]AACACTCCTATTTCC | 83860 |
rs746431450 | snp | C/G | 1.65605e-05 | 0.0028775 | missense | TAF3 | GRCh38.p7 | 10:7824452 | ATTCCGTCATTTCCT[C/G]TTAGCAAGAACAATG | 83860 |
rs746440578 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967939 | ATAAAGGTTAGGACA[A/G]CCCAGGGAAATGCCA | 83860 |
rs746453068 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937857 | CTTTTGTAGAAGTGT[C/T]GGCAAAGGAACAGTG | 83860 |
rs746475918 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970708 | ACACTTTGATGACTT[C/T]AGCAATCAGAACAAT | 83860 |
rs746489746 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974830 | CCCGTAATCCCAGCA[C/T]TTTGGGAGGTCGAGG | 83860 |
rs746492900 | in-del | -/AGAAGG | 1.82357e-05 | 0.00301952 | cds-indel | TAF3 | GRCh38.p7 | 10:7965662 | AAAAAGAGAAGGAGA[-/AGAAGG]AGAAGGAGAAGGAAA | 83860 |
rs746499573 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931704 | CTGCAATTTTATTAC[A/G]TAAATTAGTTCTGGG | 83860 |
rs746526858 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962275 | TCCTGATCATTTCCA[C/G]TGTTCTAGCTCTGAC | 83860 |
rs746550827 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932545 | TAACCAGAATCACCA[A/G]TCAAAACAAAGCATT | 83860 |
rs746560732 | snp | A/G | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817178 | CAATGTTACAGAAGC[A/G]TTCAACATTATCAAA | 83860 |
rs746582629 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920063 | CCAGCCTGGGCAACG[C/T]AGGGAGACCCATTCT | 83860 |
rs746588210 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846444 | TGGTACCAACATTTA[A/G]CATAATTTGAGGAAA | 83860 |
rs746592146 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860263 | GGTAGGTGACAGAGC[C/T]AGACCCTGTCTGGAA | 83860 |
rs746613312 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009844 | CAGGCTGGTCTCAAA[C/G]TCCTGACCTAAGGTG | 83860 |
rs746622986 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835944 | CTTCCCAGGATTCCC[C/G]TTATTGAAGCTTTTT | 83860 |
rs746632216 | snp | C/T | 1.66632e-05 | 0.0028864 | missense | TAF3 | GRCh38.p7 | 10:7964384 | AAAACCGCCCAGTCA[C/T]CAGCAATGGTCGGAA | 83860 |
rs746642474 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865553 | TAGAAACCTTGGTGC[A/G]TGCTGAGCTGTGTGG | 83860 |
rs746645206 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995106 | ATCACTACTACCACC[A/G]AGATTATTAAATGAA | 83860 |
rs746659358 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988751 | AGATTCTGTCTCTCA[-/A]GAAAAAAAAAAAAAA | 83860 |
rs746664418 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996186 | GTGGTTCTGGCTCAG[A/G]TCTGTCTGCAAGCTG | 83860 |
rs746678190 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835228 | AGCTAGAAAAAAAAG[C/T]CACACACAAAAAAGT | 83860 |
rs746685320 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873495 | TTAGGAATATCTTTT[-/A]ATGCATTAGTCACTG | 83860 |
rs746694387 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888497 | GGTCGTATCACAGGC[A/G]TGAGATCTTCTAAAG | 83860 |
rs746721123 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949218 | CTGGTTCTGTAAATC[A/G]GAGTCCACTTGCCCT | 83860 |
rs746721391 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963242 | AAGTCCTATAATAAT[C/T]CATCTCTTGATTTTT | 83860 |
rs746742115 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967625 | AGTAATGTCTATAGA[A/G]TTAGACCTGAGTTCA | 83860 |
rs746746893 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001030 | CATCATCTATGTAAC[C/T]GATCTCCTATTCTAG | 83860 |
rs746755631 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868531 | GGAGGCAGTGTGACA[C/T]AGTGGCTAATCCATG | 83860 |
rs746777928 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953310 | ACACATAAATCAAGT[A/G]GTAGAGTTTCAGGAA | 83860 |
rs746782194 | snp | A/G | 1.67911e-05 | 0.00289746 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7963984 | CATGCAGGTTCCCTT[A/G]GAAGAAGATGATGAA | 83860 |
rs746795232 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955151 | CAGACGAATAGAAAG[C/G]TATTTTTTGAAAAAA | 83860 |
rs746812077 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941861 | AGAGACATCCTTGTG[C/T]TGGATCTGGCTCTGG | 83860 |
rs746845807 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911998 | GTCATATGCACTTTC[A/G]GATCATCCAGAATTC | 83860 |
rs746874011 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854993 | CATGCTAAAATTACA[A/G]TGAAGGGGTTTTAAG | 83860 |
rs746899299 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899408 | TCCCAGGGACCTGGC[A/G]CCTCTGATCCCCAGA | 83860 |
rs746917374 | snp | A/G | 5.78687e-05 | 0.00537875 | intron-variant | TAF3 | GRCh38.p7 | 10:8009350 | GTACCTGCCGCCCGC[A/G]CGGTTAGCATGGAGA | 83860 |
rs746942926 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001955 | CAGTAAAGTTAAAAC[A/G]AAGTGACAACCAAAT | 83860 |
rs746957207 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933619 | CAGTATTCACAGTGG[C/T]GAAGTGATAGTGAAA | 83860 |
rs746962169 | snp | C/T | 1.66147e-05 | 0.0028822 | intron-variant | TAF3 | GRCh38.p7 | 10:8013697 | TTTTTTCCCATTCCC[C/T]CCATTTTTGCCGCTT | 83860 |
rs746963815 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900051 | TCCCCATTACATGTC[-/TG]TTAAAATATATTGAA | 83860 |
rs746970946 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973774 | GGAAGTCTTAAATAG[A/T]TCATAAGACTGGACC | 83860 |
rs747009785 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861586 | ATAATTCTGTACTGA[-/T]TTTTTTTTTTCATTT | 83860 |
rs747012658 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942814 | AAAATTTTTTTTTGT[C/T]GTTTTTGGGCTCTTA | 83860 |
rs747015688 | in-del | -/T | 3.02522e-05 | 0.00388911 | intron-variant | TAF3 | GRCh38.p7 | 10:7963890 | TTCCAATAATATTTA[-/T]TTTTTTCTTCCTTTT | 83860 |
rs747017482 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989074 | TGGCAGGGCTGGTCT[A/G]TTGTGAATTCAAAGC | 83860 |
rs747031651 | in-del | -/TCTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004714 | TTCAGATTTTTCCTC[-/TCTA]TCTATGATATTTTAT | 83860 |
rs747035601 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990858 | CACAGAAGACACCAG[A/G]CTGACTCACTGTCCT | 83860 |
rs747050786 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928961 | TTAAGTGTTCTGCAT[G/T]TGCCCCTACTGTTAG | 83860 |
rs747068876 | snp | C/T | 3.59079e-05 | 0.00423706 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009099 | CAGCAAGGTGGTCCC[C/T]GCCCCCGAGGCCAAG | 83860 |
rs747123043 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903390 | AGCCCCAGGCTCACT[A/G]TGTACTTCCTTTCCT | 83860 |
rs747125795 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959071 | CGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 83860 |
rs747147286 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966306 | TGCTTTAATAAGATA[A/C]GGGCACATTTCTGAG | 83860 |
rs747170959 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830999 | GATATCAGCTGATGA[C/T]GTCCAGTTTTCACTT | 83860 |
rs747181518 | snp | A/G | 1.65927e-05 | 0.00288029 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964089 | ACTGCCAGCCATGAA[A/G]CGGCCTCGGCTATTA | 83860 |
rs747200082 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832322 | GCCTGGCTTACTTCA[C/T]TTAGCAGAATTGTTT | 83860 |
rs747207026 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873914 | GAGCACTTAGGTTCC[C/T]TGTATCATCTTGGTC | 83860 |
rs747208321 | snp | C/T | 0.000267103 | 0.0115534 | missense | TAF3 | GRCh38.p7 | 10:7977269 | CAGTCGCTCTGGCCC[C/T]GAGTCCAGTTATCCC | 83860 |
rs747222452 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862060 | ACTGAGCTTTCTGCT[A/G]CACATGCAGTTAAGT | 83860 |
rs747237829 | snp | G/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819534 | GATAGAGGGACCGTG[G/T]GCAGTTGACAAGATT | 83860 |
rs747314917 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983200 | CGAAGCCCCGCTTCC[C/T]GGGCCTCCGTTATCA | 83860 |
rs747326865 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908170 | TAGACATGTACGTTT[G/T]TTCCAAAACGAGTCA | 83860 |
rs747331587 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991367 | AATAATTTATTAATG[-/T]TTTTGTAACTAATTT | 83860 |
rs747342003 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950377 | ACCTTCCAGAAGTTC[A/G]GAGAATAATTGTGTG | 83860 |
rs747369084 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883903 | GAGCCTTCTTGCTGG[C/T]GGGGAGAGGGGACTC | 83860 |
rs747398011 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825173 | TAAGATTCTAAGGAG[A/G]TATTTAAGTAATTTC | 83860 |
rs747426273 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938988 | CAAGGGAAGAGATGG[A/G]AAGTGGGAACTGACT | 83860 |
rs747448091 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866717 | AGAGCTATAGAAAAA[A/G]CCAAAGTTGCCAGGT | 83860 |
rs747449026 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909186 | ACTGGAGCTTGTCAT[A/G]AATGCAGGTTCATAA | 83860 |
rs747500494 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907256 | ATCACAGCCCTTCTG[C/T]AGGGCTGTCATTGGT | 83860 |
rs747505333 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984254 | GGCACAATACTGTTT[A/C]TTCATTAACACCAAA | 83860 |
rs747505879 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896348 | ATGGTTGTAAGTTCT[A/G]ATGCTGTCCTGTGCA | 83860 |
rs747511383 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969334 | ACTTATATTATCCAA[C/T]TGCAGTCACAGCCAT | 83860 |
rs747527525 | in-del | -/T | 3.02522e-05 | 0.00388911 | intron-variant | TAF3 | GRCh38.p7 | 10:7963889 | TTCCAATAATATTTA[-/T]TTTTTTTCTTCCTTT | 83860 |
rs747529411 | snp | C/G | 1.6615e-05 | 0.00288223 | missense | TAF3 | GRCh38.p7 | 10:7964798 | AGAATTTCAGGCCCG[C/G]AGTGTACTACTCCCA | 83860 |
rs747537987 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855113 | GTCGAGGGTCAAATG[A/G]TAAAGAACTTAGCAG | 83860 |
rs747540272 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871328 | TGTTCCTAAAACCAG[A/G]TATTCTTACAGAAAT | 83860 |
rs747547111 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003929 | ACCAAGTTTTTTGTC[G/T]TGGAAAATATAGTTA | 83860 |
rs747560512 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970638 | TTCCTGGAGATACCT[G/T]AGAGAGCACCTGTTT | 83860 |
rs747567865 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976765 | AAAATTGAACAGTTG[A/G]ATGGTACAATTACAC | 83860 |
rs747573321 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915985 | TGTCTAAAAAAAAAG[-/A]AAAAAAAAAAACCAT | 83860 |
rs747577886 | snp | C/G | 2.55262e-05 | 0.00357245 | missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818790 | CTGGGACTCGGTGCA[C/G]CTCAGCGCCTGCCAC | 83860 |
rs747585344 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839944 | TGAGAGGGACTTTAC[-/A]AAATTTAAATGGACT | 83860 |
rs747592892 | snp | A/G | 3.32851e-05 | 0.00407939 | missense | TAF3 | GRCh38.p7 | 10:7964360 | CCAGGACAGAAGACT[A/G]AATCACCTAAAACCG | 83860 |
rs747620434 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948106 | CTCACTCTGTTGCCC[C/T]GGCTGGAACGCAGTG | 83860 |
rs747638692 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996659 | GGTTTTTTTTGTGTT[A/G]TCTGTATTCTTACGT | 83860 |
rs747707474 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950485 | GTCTTACCAGATACA[A/G]TCATAGTGTTTTAGT | 83860 |
rs747710194 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836060 | TCCATCTTGGGGCCT[C/T]TCTTGGGCACGTCTT | 83860 |
rs747732914 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867322 | GATTTTTAAGTATGC[A/G]TTTTAAAATTATTTT | 83860 |
rs747742673 | in-del | -/AAG | 1.6596e-05 | 0.00288058 | cds-indel | TAF3 | GRCh38.p7 | 10:7824555 | CCATTGTGTCTTCTC[-/AAG]AAGGTTTGTGAGTGT | 83860 |
rs747748589 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849281 | GACAGTCTGACTCTA[A/C]AGAGCTTTTTTAAAA | 83860 |
rs747754694 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877957 | CTAATGTTTCTGTCA[C/G]CTTACCTGTCACAGT | 83860 |
rs747754830 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825237 | TATAAGAGTTGGAAA[A/C]GTTGCAATAAGTTCT | 83860 |
rs747761931 | snp | C/T | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016753 | GGAGGTGCCTATATA[C/T]AACTTTCCCCCCAAT | 83860 |
rs747803521 | snp | C/T | 1.99507e-05 | 0.00315832 | missense | TAF3 | GRCh38.p7 | 10:8014657 | GTGTTGGAATCATGA[C/T]TGCACCCCCAGAAGA | 83860 |
rs747825292 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951476 | GGGCTCATTCCTGTG[A/G]CAGTGGTTGCAGGTT | 83860 |
rs747837247 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998024 | TTTAAAACTGTTTTC[A/G]GTCATCACAAAAATA | 83860 |
rs747849966 | in-del | -/ATCAAATAGCTACAAAATA | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817188 | GAAGCGTTCAACATT[-/ATCAAATAGCTACAAAATA]ATCAAGTACGGCTAG | 83860 |
rs747864201 | in-del | -/AAAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935600 | AATAAATAAATAAAT[-/AAAG]CAAGCAAGCTAAAGC | 83860 |
rs747866462 | snp | A/G | 5.01324e-05 | 0.00500637 | missense | TAF3 | GRCh38.p7 | 10:7965594 | TTGAGGAGAAAGAGA[A/G]GGTGAAGGAGAAAGA | 83860 |
rs747884610 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989157 | GCAAGCTCTCAGTGG[C/G]CCAGCTGAGATCACG | 83860 |
rs747909797 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859539 | CACTGGGCACTGGCC[A/G]GGTTTCACCTCCTCC | 83860 |
rs747934839 | snp | C/T | 1.66136e-05 | 0.00288211 | missense | TAF3 | GRCh38.p7 | 10:7964900 | AGTTCCGATAACTCA[C/T]GGACAATGGATGCCT | 83860 |
rs747948323 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959790 | TCTGATAGAATTGCA[C/T]ATTAGTAAAATAATA | 83860 |
rs747963404 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912774 | GCCAGTGGCTTAATC[C/T]GTCAGTCCAGGACCT | 83860 |
rs747970820 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932868 | TTTTTTTGTGTGGAC[A/G]GGGATCTCAATATAT | 83860 |
rs748001286 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847920 | GACTACAGGCACCCA[C/T]CACCACACCCAGCTA | 83860 |
rs748028819 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829749 | TTTCTCTTCTATCCC[C/T]TCTTCCCCTACTGTG | 83860 |
rs748031184 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934009 | GTGTCAATGGCTTGT[A/G]GGAAAATCCCAGAGA | 83860 |
rs748031591 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889266 | CTCTTCTCACTCTCC[A/C]CATTTGGGGAATGAT | 83860 |
rs748044114 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876859 | AGTGCATGATTCTTC[C/T]TCCAGACTCTTTTCT | 83860 |
rs748082689 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855452 | ATGCCGAGATGTCCA[G/T]CCTCCTTCCATTTGA | 83860 |
rs748083671 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975281 | GTATTTCCTGTGGAG[A/T]TAGATGTGTAGAAGG | 83860 |
rs748083733 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990221 | CACTGAGGAACCTTG[A/T]GAGTCGCTAATGCCA | 83860 |
rs748085151 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962404 | GTGACTTTTCCCAAC[A/G]CATACCCCACACGTT | 83860 |
rs748088468 | snp | C/T | 6.33734e-05 | 0.00562874 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009264 | CTCCCCGGGTCCCGC[C/T]GCCTCCGGGGCCAGT | 83860 |
rs748162072 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978740 | CTCTAAGAGGAAGAT[A/G]TTGTTATCCATCATT | 83860 |
rs748171057 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917642 | TCTGGAGAATAGGTC[A/G]GGTTCTGAGGCCGTC | 83860 |
rs748176968 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821563 | GTATTAGAAGTTACC[A/G]TTAATTCAAATAATG | 83860 |
rs748180812 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982939 | TTCATCTCTAGTGGA[A/G]ACACTCCTATTTCCT | 83860 |
rs748203631 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935560 | CTGCACTCCAGCCTG[A/G]GTGACAGAGAGAGAC | 83860 |
rs748208525 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946278 | CCTGCTCCTTCCCAT[A/G]CCTCAGACACAAAAC | 83860 |
rs748254912 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923836 | ATAATTGACTTTTTA[A/G]TACAGAAAGCAAGGC | 83860 |
rs748255614 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904466 | TCATTGCATATTCTA[C/T]ACCTAGTAGTCTATT | 83860 |
rs748261379 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947617 | GACCTGGAGGAACAG[C/T]ACTGGGGCTGCTGCG | 83860 |
rs748264353 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007367 | TATTGTTTATGGACA[C/T]CTACAAAGGCAGGAA | 83860 |
rs748277739 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826337 | TTCCATAATAAAATT[A/C]TCTTAAAGTGCTATG | 83860 |
rs748283905 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891953 | ATAGTATTACAATAT[A/G]TATATAAATTGTAAC | 83860 |
rs748285427 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838742 | GGCCCCCTAACATCC[A/G]ACGCTATAAGCCTCC | 83860 |
rs748291820 | snp | C/T | 1.67621e-05 | 0.00289495 | missense | TAF3 | GRCh38.p7 | 10:7965008 | CCGTCAGTGTCTCCT[C/T]CCACTCCCGAACCTC | 83860 |
rs748304529 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945396 | AAAAACTGTTATTTT[C/G]CAGGTCTTTTGTTTG | 83860 |
rs748311086 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820554 | GCGTGGAGTGCAGTG[C/G]TGCGATCTTAGCTCT | 83860 |
rs748337208 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893040 | GATCAGGCTGGTCTC[C/T]ACCTCCTGACCTCCG | 83860 |
rs748339439 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936735 | CTCTTGGTGTTGTAC[A/G/T]TTCCATGGGTTTGGA | 83860 |
rs748342678 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898142 | ACTCCAAGTAATAGA[A/T]TATGGAAGTACAAAT | 83860 |
rs748366302 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852365 | TTAGGGTCCAAATAA[C/T]ATCCACACGTTGTGA | 83860 |
rs748378534 | snp | C/T | 1.65652e-05 | 0.0028779 | missense | TAF3 | GRCh38.p7 | 10:7824524 | AGAAAAGAATACATT[C/T]CTGATTACCTGCCAC | 83860 |
rs748383469 | snp | A/G | 1.70766e-05 | 0.00292199 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7963957 | CACTGATGGAGGCAC[A/G]TCAGCAGAAGCCATG | 83860 |
rs748389022 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864251 | CTTCCCTCCCTTACC[C/T]CAACCTGTGGCAACT | 83860 |
rs748409256 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957376 | GCTATTGGTTTTACA[A/G]AGATCACGGGGAGGA | 83860 |
rs748414559 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012909 | TTATTGTAAACACTT[C/T]GGAAGTTACCTTTTT | 83860 |
rs748444396 | snp | C/G | 1.66183e-05 | 0.00288251 | missense | TAF3 | GRCh38.p7 | 10:7964672 | GCAGATAAAACGATT[C/G]AGGCCTCTATCGATG | 83860 |
rs748451822 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966372 | GAAAGTAATCCCACA[G/T]GGCAGAAATGTTTGA | 83860 |
rs748456956 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961340 | TGATGTTCTTTATGA[-/T]TTACTAAGTACTTCC | 83860 |
rs748491157 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940205 | TTCTATTTTCAACCA[C/T]GCTGTTAGGTCAGAG | 83860 |
rs748514261 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886330 | GACTGGCATGACCTG[A/G]TCCTTCTCCAAACCC | 83860 |
rs748532201 | snp | A/G | 1.89091e-05 | 0.00307477 | missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818767 | GCGCAGATCTGCCAG[A/G]CGCTGGGCTGGGACT | 83860 |
rs748597096 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842565 | TAAATTTTTTAGATG[C/T]GGGCTTAAAGCTATA | 83860 |
rs748628600 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005736 | AGAAGCAGTGTTTTA[A/C]AATTTTAGTCTAACC | 83860 |
rs748629849 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916019 | GTTTTTAAAGCCCCA[A/G]TCTTGTTAGGAGTCT | 83860 |
rs748662398 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004924 | ACTAATTAGACCTTT[A/T]ATTGTATTCTCTTTG | 83860 |
rs748671076 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886475 | CAAAATATATAATAA[-/C]CAAAGAAAAGTTTGG | 83860 |
rs748674472 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844261 | TCCATTATTGTCCAT[C/T]TTCCTTCCATGTTTT | 83860 |
rs748677449 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992042 | CATTTTCATGTGAAA[A/G]CATCTTTTACTAAAT | 83860 |
rs748678174 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943076 | CGAAAGTCTGTCCTT[-/A]ACTTAGCAGCGGTTG | 83860 |
rs748682818 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834614 | CATGCAGATTTTCCA[A/G]TTCATATTTAGGACT | 83860 |
rs748704346 | snp | A/G | 1.66402e-05 | 0.00288441 | missense | TAF3 | GRCh38.p7 | 10:7965444 | ATAAAGGCAGAGAAG[A/G]TAAGATGAAAGCCCC | 83860 |
rs748712030 | snp | A/G | 3.34197e-05 | 0.00408763 | missense | TAF3 | GRCh38.p7 | 10:7964583 | GTAAAGAGACTATCC[A/G]GGTAAAACAAATACA | 83860 |
rs748728447 | in-del | -/TTGTTCTAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892410 | ATAATGTACTTTTCT[-/TTGTTCTAC]TTGATTACAAAATTT | 83860 |
rs748730304 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999662 | GGGTTTCACCATGTT[C/G]GCCAGGCTGGTCTCA | 83860 |
rs748759515 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952882 | GTCTAATTTCTGTTA[A/C]ATTATAGACAGGACA | 83860 |
rs748775901 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885251 | TATATAAATTTTGAC[-/AC]ACACACACACACACA | 83860 |
rs748796684 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833050 | CTGTGGTGCTATTAA[A/C]GGCTGAATAGTATTC | 83860 |
rs748815845 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923499 | TGTGCCATATCTTTA[A/T]GTTTAAAATATCTCA | 83860 |
rs748824240 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826252 | AGCCCAGAACCAAAA[C/T]TAGGACTTTGATCAT | 83860 |
rs748852021 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896570 | CTCTCATTCGACAGT[C/T]GCATTTGGGGACAGA | 83860 |
rs748854580 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940474 | ATAAGCTTATAGTTT[C/T]CTAATCCTGGATAAC | 83860 |
rs748869666 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907348 | TGTGCTGTTCCTATC[A/C]TTGCTGGCAGATGAG | 83860 |
rs748873644 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929361 | AAGTAAGATACATAC[A/G]AGGAAGTAGTACCTC | 83860 |
rs748883255 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950045 | ATTTTTCTAATAATA[G/T]CACTGCTGGAGAAAG | 83860 |
rs748910949 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929859 | ACAAGAAAAGAGAAC[A/G]GTAAGAGTAGGTCCA | 83860 |
rs748922523 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985909 | CTGCCTTGGCCTCCC[C/G]AGTAGCTGGGACTAT | 83860 |
rs748936516 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844502 | CTGCCTCAGCCTCCT[G/T]AGTAGTTGGGATTAC | 83860 |
rs748948139 | snp | A/C | 1.65627e-05 | 0.00287769 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8013748 | CCGAGATGAGTGGGG[A/C]AATCAGATCTGGATC | 83860 |
rs748958349 | snp | C/T | 9.94711e-05 | 0.00705164 | intron-variant | TAF3 | GRCh38.p7 | 10:8013866 | GCGCCCTGCCGGCCA[C/T]ACTCATTAGGCAGCA | 83860 |
rs748963356 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868126 | GGAGAAAATCCACAT[A/G]TAAGGGGGCATGTGT | 83860 |
rs748985630 | snp | C/T | 1.68499e-05 | 0.00290253 | missense | TAF3 | GRCh38.p7 | 10:7965270 | AGGAAGAGGCAGATC[C/T]CTACAAGTTTAAAAT | 83860 |
rs748994575 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991529 | TTATTAACAGAGATA[C/T]AATATTAAACAGGCA | 83860 |
rs749009055 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894233 | TTCTCCTACCCCTAA[G/T]CAATACAAATTCTCC | 83860 |
rs749010873 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914637 | TTTCTGTATTTGGAC[A/T]TTTACTGTAAATTGT | 83860 |
rs749023099 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820452 | TTACATATTGAGTTC[C/T]AAAAATGTATATGTT | 83860 |
rs749048545 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976722 | TTGTTTTCTTTTACA[A/G]CATTTCAGATTGTTT | 83860 |
rs749102559 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963531 | TACTTTTTAAACACT[A/G]TCAATAATTTCCTTT | 83860 |
rs749103514 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934144 | TTCGGAAGAATTAGA[A/C]ACTGAAAGGAAAGAA | 83860 |
rs749107286 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930855 | TATACTTTTGTATAT[-/A]AAAATATAAGGGCTT | 83860 |
rs749108985 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903037 | ACCAGCCTGGACAAC[A/G]TAGTAGGACCCCATC | 83860 |
rs749119909 | in-del | -/TTTTTAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820663 | CATGCCTGGCTAATC[-/TTTTTAT]TTTTTATTTTTTGTA | 83860 |
rs749146117 | snp | A/C | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819251 | CCTTTTTCTCCCTTG[A/C]CCGCAAACTACTACA | 83860 |
rs749157144 | snp | C/T | 9.95834e-05 | 0.00705562 | missense | TAF3 | GRCh38.p7 | 10:7964231 | AGTACAGACTTGGCA[C/T]CTCCCTCACCCGAGC | 83860 |
rs749158279 | in-del | -/TTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859869 | CGTTTCCCAGATAAC[-/TTA]TTATTTCATAATGAT | 83860 |
rs749165660 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848129 | TCTATGCATTCTTCA[C/T]TAAATGGCTTAACAA | 83860 |
rs749185357 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878192 | GTGAGGCCTAAAGCT[C/T]GTACAATTTTGGGAG | 83860 |
rs749242538 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998636 | CTGAAGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 83860 |
rs749255211 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849443 | TAGATCTTGCACTTC[C/T]GGGACGATTTAGGGT | 83860 |
rs749274392 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949525 | TCTTTGACACTTGGA[-/T]TTTAGAATGTCCACT | 83860 |
rs749286860 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981844 | TAATACTTGTAATGT[C/T]TAAATTTTTTCTATA | 83860 |
rs749312770 | snp | A/G | 1.65614e-05 | 0.00287757 | missense | TAF3 | GRCh38.p7 | 10:7824513 | ATGCAGAGGAAAGAA[A/G]AGAATACATTCCTGA | 83860 |
rs749313219 | snp | C/T | 3.32524e-05 | 0.00407739 | missense | TAF3 | GRCh38.p7 | 10:7964318 | ACAAAGTCATTTACA[C/T]CTAAAACAAAGACTA | 83860 |
rs749359457 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847984 | ATGGTGTCCAGGCTG[-/A]ATCGCAAACTCCTGA | 83860 |
rs749359559 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924861 | TATCACACAAACATG[C/T]TCATATCTCACTTAA | 83860 |
rs749380231 | snp | A/C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894279 | GTCAGCAGGGACAGT[A/C/T]GGCCCTCAGGGAACA | 83860 |
rs749385714 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893324 | TACAAGCCTAATAGA[G/T]AAACTTTTTTTTAAA | 83860 |
rs749390259 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013164 | TTTACTAAAAATGTC[A/G]TAAAGGGAATGGAAA | 83860 |
rs749417274 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822870 | AGAAAAACTTGCTTT[G/T]GTAAAGAAAAAAATC | 83860 |
rs749420041 | snp | A/G | 2.67419e-05 | 0.00365653 | missense | TAF3 | GRCh38.p7 | 10:8014723 | AGAAGGACAAAAAGC[A/G]CAAGAAGAGGAAGCA | 83860 |
rs749422300 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961710 | TATATTTCAGCTGCC[A/G]AGTAGGCATTGCAGA | 83860 |
rs749435986 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852481 | TTGTTTGTCCTGTAG[A/C]GTTTTTTATAGTCTG | 83860 |
rs749437125 | snp | C/T | 1.73848e-05 | 0.00294824 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009261 | GCCCTCCCCGGGTCC[C/T]GCCGCCTCCGGGGCC | 83860 |
rs749461014 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925951 | AGGTGCAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 83860 |
rs749484666 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882277 | TTTTGGTCAATCTAA[C/T]GTGTATTCCTCATTT | 83860 |
rs749491126 | snp | A/G | 3.31917e-05 | 0.00407367 | missense | TAF3 | GRCh38.p7 | 10:7964828 | AAAGCTTCCACTTCC[A/G]CGAACAATTTCACAA | 83860 |
rs749505345 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870162 | CCATTACATTACTGA[A/G]TAGAGGTTTAACTTT | 83860 |
rs749521823 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935626 | GCTAAAGCTAAGTAG[A/C]GGGCCAGAGAATACT | 83860 |
rs749528054 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853641 | GCTTTAGATTAAACT[A/G]GAGGTCAGCAAACTG | 83860 |
rs749545059 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002329 | TATCCCGTCGCACAT[C/T]GTAAAGCATATTATT | 83860 |
rs749573126 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968883 | ATTGTTTTTCTATTA[A/G]TGATGATAAATCCAG | 83860 |
rs749576209 | snp | C/T | 1.73703e-05 | 0.00294701 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964497 | CAAGGTCACGACTCA[C/T]ATTCCCCAAACACCT | 83860 |
rs749588517 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982707 | CTTGACTGAAATACA[-/T]TTTTTTTTTAAAGGA | 83860 |
rs749605178 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005909 | AAAATCAGACTGCCT[A/T]GTTTAAATCCTGGCC | 83860 |
rs749614753 | snp | C/T | 1.67136e-05 | 0.00289076 | missense | TAF3 | GRCh38.p7 | 10:7977257 | TAAAAGTGGAACCAG[C/T]CGCTCTGGCCCCGAG | 83860 |
rs749625142 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844272 | CCATTTTCCTTCCAT[A/G]TTTTGATTTTTAAAC | 83860 |
rs749630421 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930284 | TGTAGGTAAGAGGTG[G/T]GTGGGTAGAAAGGGA | 83860 |
rs749660017 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845771 | ATTCCTTAGTATTGA[A/G]CATCTTAGTCTTTTC | 83860 |
rs749685529 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917772 | GGAAATGAGGAAAGA[A/T]GGGAATGAAGAAGGA | 83860 |
rs749688038 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946640 | AGGTGGGAGGATCAC[C/T]TGGACCCAGGAGGTG | 83860 |
rs749741384 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900757 | GAAGGTATAGGGTAG[C/G]GTAGTGTTTCACTGT | 83860 |
rs749748234 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905581 | GCAAAGCAATATACT[C/G]CTTTAAAAACTTAAG | 83860 |
rs749756102 | snp | A/C/T | 0.00151417 | 0.0274735 | missense | TAF3 | GRCh38.p7 | 10:8009251 | CTGCCCTGCTGCCCT[A/C/T]CCCGGGTCCCGCCGC | 83860 |
rs749759752 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821991 | TAGTTCATTCCAAGG[G/T]TGTCTGAGTAAAATG | 83860 |
rs749772893 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875319 | AAGTCCTATAAATGA[C/T]GTTCTTTGAGCCTTT | 83860 |
rs749779359 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864477 | TTTTAAAAAAATACT[A/G]CAGTATATTATTCTT | 83860 |
rs749807461 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994505 | TAATATTACTGTTAC[C/G]TATTTATTTATTGTT | 83860 |
rs749819289 | in-del | -/CT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883916 | GGCGGGGAGAGGGGA[-/CT]CTCAGAGTCACCAGG | 83860 |
rs749821969 | in-del | -/AAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959164 | CACACACACACACAC[-/AAAA]AAAGTTTCAGGCTTT | 83860 |
rs749833029 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922434 | TCTTTTCTGTAAAAC[A/G]TAGATGATTATCAAG | 83860 |
rs749841897 | in-del | -/AAAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994810 | CTACTAAAAATACCA[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 83860 |
rs749888353 | snp | C/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015585 | TAATTCTGGCTTTCT[C/G]TGAAATCCACTGTGA | 83860 |
rs749921344 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954883 | AATGAGTGAATTAGT[C/T]CTAGTTAACACAGAG | 83860 |
rs749923132 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958637 | GGAGTGGAGAAAGCA[A/G]GGGTGGATGGGAAAG | 83860 |
rs749947461 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912419 | ATGATAGTTTTTATG[A/G]GTAAGAAACAACATG | 83860 |
rs749947625 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829236 | TTAGTTTGGAGAGTT[C/T]ACTCACATCTGAACC | 83860 |
rs749978770 | snp | A/G | 7.03185e-05 | 0.00592911 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818887 | CTCTGTGAGTACCGG[A/G]CTGGGTGCGGGAGGG | 83860 |
rs749987546 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926636 | TCTTTTAAAATCTGT[A/G]TAATTACTCTGGTCA | 83860 |
rs749991379 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856544 | TTATAGAACCAGTCC[A/G]GGAAGCCTAATATCT | 83860 |
rs750027345 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943292 | CATCACGTTCTGCTT[C/G]CTCCTTAGCATTGCA | 83860 |
rs750028118 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912178 | AAGAGCCAACAGTTA[A/C]AATAAAATATGAAGT | 83860 |
rs750035794 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830582 | TCCACCTCCTGGGTT[C/T]AAGCGATTCTCCTGC | 83860 |
rs750047162 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876394 | AACCCTTGTAAAGAG[G/T]TATTTTCAATGAAAT | 83860 |
rs750052832 | snp | C/G | 3.58648e-05 | 0.00423451 | intron-variant | TAF3 | GRCh38.p7 | 10:8009034 | CGGGTTTGGTTCGAT[C/G]ATGATCCTGTTTTGA | 83860 |
rs750081059 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003114 | TGACAACTGAATCAC[G/T]TAGACCTTTTATGTG | 83860 |
rs750108079 | snp | A/C | 1.66208e-05 | 0.00288273 | missense | TAF3 | GRCh38.p7 | 10:7964658 | AAAAGGCTGTGGTAG[A/C]AGATAAAACGATTGA | 83860 |
rs750110643 | in-del | -/AT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973989 | AAAAAGTAGCCGGGC[-/AT]GGTGGCATGCACCTG | 83860 |
rs750127395 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935138 | AAAAATCAGCTGTGC[A/G]TGCTGGTGCGCGCCT | 83860 |
rs750130364 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989788 | ACCCCAGATGCAGAG[A/G]ATGATTGTTAGTTAG | 83860 |
rs750139180 | snp | A/G | 1.80133e-05 | 0.00300105 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009126 | CAAGCCGGCGCCCTC[A/G]CAGAACAGGCCGAAG | 83860 |
rs750208896 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822308 | CTACCAGGTTTTGGT[C/T]TGAGGCTGCAAAGCA | 83860 |
rs750220657 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845220 | TGTTTTAAAATTTTT[A/C]GTTGAAATGTGGGAA | 83860 |
rs750241647 | snp | A/G | 1.6617e-05 | 0.00288239 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964299 | AACTGCAAAACCATT[A/G]GAAACAAAGTCATTT | 83860 |
rs750250992 | snp | A/G | 3.66838e-05 | 0.00428259 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965667 | AGAGAAGGAGAAGAA[A/G]GAGAAGGAAAGAGAG | 83860 |
rs750252001 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936289 | CTCTTTTTCTTTTTT[A/G]TAATTTACTAGGCAT | 83860 |
rs750253091 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942183 | GTGAGAGCCAGGGAA[A/G]AGGAGAGTCAGTCTA | 83860 |
rs750260048 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821434 | ATTGGAGACATAAAA[G/T]TACTAAGATACAATC | 83860 |
rs750265069 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948367 | GTGTTGGGATTACAG[G/T]CATGAACCAGTGCGC | 83860 |
rs750306982 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937362 | GTGTTGGCAGTGTTT[C/T]GGCTTTTGGTCATTC | 83860 |
rs750352733 | in-del | -/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836861 | CACATTATAAAACAC[-/TT]TGTTGGCTCTCCAAC | 83860 |
rs750383050 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863576 | GATCGCCCCACTGCA[C/T]TCCAGCCTGATGACC | 83860 |
rs750383607 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864709 | TGGTCATCAGTTTTT[C/T]ATCATCTATTTGTTT | 83860 |
rs750393942 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881879 | GATAACTGATTTTTG[A/T]GATTCTTGAGCAGAG | 83860 |
rs750394513 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982581 | TTTTTTGTAGTTTTA[G/T]TAGAGATGGGGTTTC | 83860 |
rs750405590 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895235 | AACCCCTTGTTTTTA[C/T]TGGCCCATTGGACAT | 83860 |
rs750409856 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013967 | GGACAGTACATGGAG[A/T]CAAATCACTGAGCCT | 83860 |
rs750432438 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967180 | TGCAGAGAGACTTCA[C/T]GTGGTGAGGGGTTTG | 83860 |
rs750437687 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834243 | CTTTTGTCACCCTGC[A/G]CTTTTGGGGCCAAAT | 83860 |
rs750451523 | in-del | -/GAAAGA | 0.000364783 | 0.0135003 | cds-indel | TAF3 | GRCh38.p7 | 10:7965187 | GGAGAAGGATAAAGT[-/GAAAGA]GAAAGAGAAAGACAA | 83860 |
rs750466540 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006169 | ACCCCGTCTCTACTG[-/AA]AAAAAAAATACACAC | 83860 |
rs750468838 | in-del | -/AGTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955555 | TGCGTCTGTGTAGTT[-/AGTC]AGATAAAAAGCTTCT | 83860 |
rs750489543 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885990 | CTGGTGTGTAGTGGC[A/G]CGACGATGGCTCACT | 83860 |
rs750493373 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993237 | AGGCTGGAATGCAGT[A/G]GTACGATCATAACTC | 83860 |
rs750510315 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825073 | TTTTGATTATAAAAT[A/G]ATAGCTAATCAGGTA | 83860 |
rs750511833 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014230 | AAGACTGCTTATCTG[-/T]TTTTTTAGACCTCTT | 83860 |
rs750567767 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856962 | CTAATGAGATAAGCA[A/G]TATCCTTGTAGTAAA | 83860 |
rs750578735 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867128 | GCCAGGCATGGTGGC[A/C]TGCCCCTGTCATCCC | 83860 |
rs750579525 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887717 | AAAGGCTTCAATCCA[A/G]GCTAAAATCGGGGGG | 83860 |
rs750581407 | in-del | -/ACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991187 | TATATATGTATAGAT[-/ACAC]ACACACACATATACA | 83860 |
rs750596813 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843810 | TTTTCACTACATATT[A/G/T]TGTAGTGAAAATATA | 83860 |
rs750632740 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886776 | GAGAGATGCACTTTC[A/G]TATTTCTGTACTTGT | 83860 |
rs750633365 | in-del | -/CT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832059 | AACATTTAAAACTTA[-/CT]CTCTTAATGATTTTC | 83860 |
rs750658566 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004564 | AAGATGTTTTCAAAG[A/G]CATAATTTATTTTTC | 83860 |
rs750666118 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856198 | GCAGAATCAGAAAAG[A/G]TTTTGGCTGGGCGCA | 83860 |
rs750681978 | snp | A/G | 3.37752e-05 | 0.00410932 | missense | TAF3 | GRCh38.p7 | 10:7964447 | GAAAAGAAATCACCT[A/G]GACGTTCCAAGAGCC | 83860 |
rs750731714 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009544 | CTCCTGGGCCCAAGC[C/G]ATCCTCCTGCATTAG | 83860 |
rs750741943 | snp | A/G | 3.1317e-05 | 0.00395696 | intron-variant | TAF3 | GRCh38.p7 | 10:7963880 | TTTTGTTACATTCCA[A/G]TAATATTTATTTTTT | 83860 |
rs750756348 | in-del | -/C | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817533 | GGCATATTTAAGAAA[-/C]CGCATAGTTCAGCCA | 83860 |
rs750757154 | snp | C/T | 3.37291e-05 | 0.00410651 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965064 | CAAGCTGCCTTCCTC[C/T]GTGGAGGTAAAGAAG | 83860 |
rs750759663 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979217 | GGTGTGGTGGCAGGT[A/G]CCTGTAGTCCCAGCT | 83860 |
rs750792516 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977343 | GTATAAACGTTTTGA[A/G]TCAGGGTGAAACAAA | 83860 |
rs750796859 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835798 | TTCCCTTGCATAGAT[A/G]CCTCATACTCGGGTC | 83860 |
rs750797519 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933874 | ATGGATTCAAAGATG[C/G]ACGTTTTCCCCCCGA | 83860 |
rs750798587 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962912 | CTTAGTTAAAATGTG[C/T]TGGGAGAAATAATCT | 83860 |
rs750814898 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885358 | AAATATAGTTAGATT[C/T]GTTTATTTCCATTTA | 83860 |
rs750833962 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818306 | AACACTGGCGTTTTC[C/G]TCACCGCTGTCCCCC | 83860 |
rs750837425 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847656 | TGCTGTGTTGCCCTG[A/G]TTGGTCTCAAACTCC | 83860 |
rs750841753 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872938 | GAATCCAAGCCTGAA[-/T]TTTTGAGTTGTCAGA | 83860 |
rs750842594 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920781 | AATAAAGCTTATCTT[A/G]CCAAATATTTGAAGG | 83860 |
rs750844066 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919917 | CCCTCATATTCTGTA[A/T]TGAGTTTTTCATTTG | 83860 |
rs750847544 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976609 | TTAGTTTCACCATGT[C/T]GGCCAAACTGATCTC | 83860 |
rs750869052 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891053 | CCCTTTGCATGTCTG[C/T]AGCAGGCAGTGAGTG | 83860 |
rs750881624 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890024 | TGGTTACTGCTGTAT[G/T]TATAATTTTTCCAGT | 83860 |
rs750924985 | in-del | -/CTAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924743 | CACCCCAACAGAACA[-/CTAT]CTGTGTTTTTTTTTT | 83860 |
rs750931566 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909087 | CCTGTCACCTCTCCC[A/G]TGGAGGCCTGCCAGG | 83860 |
rs750946711 | snp | C/T | 2.08171e-05 | 0.00322616 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009318 | GGTGACTGAGACGGT[C/T]AGCACCTACGTGGTG | 83860 |
rs750956642 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854665 | CTCTAATGGGGGGGC[A/G]GGGGGAGGGGAGCTT | 83860 |
rs750959300 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950292 | ATAGAACGACCCAGG[A/G]AAGAGTGTTCCCATG | 83860 |
rs750967914 | snp | A/G | 0.000102548 | 0.00715986 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964551 | GACTCCTTCAGCTAC[A/G]CTCAGTGAAAAAATC | 83860 |
rs751019261 | snp | A/C | 6.82408e-05 | 0.00584087 | intron-variant | TAF3 | GRCh38.p7 | 10:7977361 | AGGGTGAAACAAATG[A/C]AATTTAACCTTCTCT | 83860 |
rs751027067 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859596 | ATAAAGAACCTTAGA[C/T]GCCCTCCATTTGCCC | 83860 |
rs751037946 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821492 | CCAGAATGTCAGGAA[A/G]CAACAAACTGATGGT | 83860 |
rs751066042 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945019 | TGAAAACATAGCATC[A/G]GACTACATAACTGTA | 83860 |
rs751070415 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004285 | ACTCCTGGCCTCAAG[C/T]GATCCACCCACCTCG | 83860 |
rs751090634 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936692 | GCACATCATAGTCAG[A/C]AGAGACCACAGTTTA | 83860 |
rs751103978 | snp | A/G | 4.98873e-05 | 0.00499411 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964641 | CAGTGAGAATCAGCC[A/G]AAAAAGGCTGTGGTA | 83860 |
rs751119964 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914674 | AATCTATTATAAATG[G/T]CTAGTTTCTTCGTAT | 83860 |
rs751126059 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902610 | TAATGTCAGGCTCTC[C/T]GGGTGCTGGGGGATG | 83860 |
rs751138906 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893689 | CCCTTTGCTTCTAGC[A/G]TAGGCCTGGCCTATC | 83860 |
rs751148842 | in-del | -/AGCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850560 | CATGCATGTAATCCC[-/AGCT]AGCTGCTTGGAAGGC | 83860 |
rs751168894 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849079 | ATTAAACTTATGAAC[C/T]GCAACAACACTTACA | 83860 |
rs751169536 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945802 | AAAGTCGCCCTTTTT[C/G]TCTCCACACACATTA | 83860 |
rs751175199 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903949 | TGAGAATATTTTACG[A/G]TATTGTAGGTATCTG | 83860 |
rs751201023 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933926 | GATGCATCTCACAGT[C/T]ACTGCCTGGCAGCTG | 83860 |
rs751247593 | in-del | -/CACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959157 | ACACACACACACACA[-/CACAC]ACAAAAAAAGTTTCA | 83860 |
rs751251103 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010373 | AATATCAATCTGTAA[A/T]TGTAGAGACGCATGG | 83860 |
rs751274230 | snp | A/G/T | 4.97239e-05 | 0.00498597 | intron-variant | TAF3 | GRCh38.p7 | 10:8013853 | GTGAGTGCCCAGGGC[A/G/T]CCCTGCCGGCCACAC | 83860 |
rs751292283 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977739 | CTCTTTTTGCTCAGA[C/T]GGCACATGGTTTTAT | 83860 |
rs751298885 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937507 | GTAAAGTGTCTGTTC[A/C]GGTCTTTTGCCCATT | 83860 |
rs751311956 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009995 | CGGCTCACTGCAGCC[C/G]CTGCCTCCCAGGCTC | 83860 |
rs751334269 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846239 | TGGCATTACAGGCAT[A/G]AGCCACTGCGCCCGG | 83860 |
rs751339448 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823823 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 83860 |
rs751352038 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925706 | TGGTAGACTGAGGCA[A/G]GAGAATCATTTGAAC | 83860 |
rs751368290 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853552 | GGAAATATTCTTCAA[C/T]TGTTATCTGATTCAG | 83860 |
rs751371145 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968701 | TTAGAGAGATTAGTA[A/G]ACTTGCCCAAGATCA | 83860 |
rs751372564 | in-del | -/ATGATTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888331 | AGTGATGCACATAAT[-/ATGATTC]ATTGAGACAGTGGAG | 83860 |
rs751387268 | snp | A/G | 8.0048e-05 | 0.00632595 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818844 | CTATCTGCAGCAGCT[A/G]GGCCGGGGCTGCCAT | 83860 |
rs751389382 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950018 | ATGATACATGGTGAA[A/G]TCGTTTCTCTCATTT | 83860 |
rs751406227 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879291 | GTAGATTATTAATTA[C/T]AAACTTACCTATGAA | 83860 |
rs751412897 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938500 | ATGGATGGTGAGTGG[A/G]AAGGCTTGAAAACTC | 83860 |
rs751414208 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866105 | GTTTTTTCTGGATCG[C/T]AAAGTAATTTCTGAA | 83860 |
rs751423832 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829180 | AATTTAAAATAGACT[A/G]TTTTTTAGAACAGTT | 83860 |
rs751513979 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883431 | TCCTGTGATACTGAT[A/T]TGATGGTAATTTTAT | 83860 |
rs751515973 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896088 | TAGTTGAAGTAACTG[C/T]ATCGGTTGCTGCTGA | 83860 |
rs751518872 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854463 | GAAGTTAACATGCTA[A/C]AGAGACAAAGCTAAC | 83860 |
rs751542369 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016207 | AGGCCCATGTGCTGG[A/G]TCTGTTGGATGCTAG | 83860 |
rs751546398 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889894 | TGCCACAGGTCCTGT[C/T]CTCATTTGGATTTTG | 83860 |
rs751553476 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970098 | GATAAGTAGAGGACT[A/G]CAACAGTTCCTGAAT | 83860 |
rs751582251 | snp | A/G | 6.64628e-05 | 0.00576429 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964290 | ACAAATGCCAACTGC[A/G]AAACCATTAGAAACA | 83860 |
rs751589868 | snp | A/G | 3.67431e-05 | 0.00428605 | utr-variant-5-prime, stop-gained, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818693 | AGCAAGGGCTGCGGT[A/G]GCGTCCACGCAGCGG | 83860 |
rs751595066 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936833 | CTCTTTGCTGCTTCT[-/C]TTCATCCCTCCCTCC | 83860 |
rs751600182 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003253 | GGTTTTTTTTTTATC[A/G]TTCCTTTTTTCCTCA | 83860 |
rs751629557 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941130 | AATATGAAGCTGAAG[G/T]TAAGGCATGGGAATC | 83860 |
rs751631621 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911883 | ACTCCTTTCTGTAAT[A/G]GGCCTAGCTTGCTTT | 83860 |
rs751641279 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971439 | GCTACCCTAGCTAGT[A/G]TACATATATGGTGTT | 83860 |
rs751643009 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986464 | TTAGGGTAACTTGAA[G/T]GGAGGCAAAAACTAT | 83860 |
rs751645179 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864126 | TTAGGTTCACTCTTG[A/G]TGTTGTACATTCTCT | 83860 |
rs751665302 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921794 | TGAATATTGTAGAAG[A/G]AAATTTGGAAGACTG | 83860 |
rs751721524 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873619 | GACATCCGAGTTCTC[-/C]CCCCCCCCCCGTCAA | 83860 |
rs751752004 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871704 | CCACCTCAGCCTCCC[-/A]AAGTGCTGGAATTAC | 83860 |
rs751758422 | snp | A/T | 1.66921e-05 | 0.00288891 | missense | TAF3 | GRCh38.p7 | 10:7965396 | AGAAAGGCAAGAAAG[A/T]TAAAGATAAGAGAGA | 83860 |
rs751787308 | snp | C/G/T | 7.52612e-05 | 0.00613399 | intron-variant | TAF3 | GRCh38.p7 | 10:8014615 | ATAAAAGTTGCTTAT[C/G/T]TGAGCTTGTTTTCAC | 83860 |
rs751806409 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011502 | GCTGGTCTCAAACTC[C/T]TGGGCTCAAGCAGTC | 83860 |
rs751807045 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874931 | AAAATCCTTTCTAAA[C/G]TTTTTAGACTTCTAG | 83860 |
rs751809985 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845375 | GTAGTGTTGAATTTT[A/G]TGTCCTCCGTTTTTC | 83860 |
rs751813983 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887863 | GAATTGGAAAAGTGA[A/G]GCATTGGAAGCTTTT | 83860 |
rs751814536 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851725 | ATATAACTCTAAAAG[A/G]TAACTATTTTTGGCA | 83860 |
rs751831940 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007066 | GAAACTTCATTTCTA[A/G]GGATGGGGCTTGGAG | 83860 |
rs751833618 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993025 | ATACAGACATTTTCC[G/T]TGTTACCATCTAATA | 83860 |
rs751850162 | snp | C/T | 1.67049e-05 | 0.00289002 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965508 | GGCCCTGCCCTTGTT[C/T]AGCCCTGCCACAGCC | 83860 |
rs751870831 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876964 | ATAAAACTGTCATCC[-/T]GATTTTCAGATCTCT | 83860 |
rs751887737 | snp | C/T | 4.98078e-05 | 0.00499013 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964872 | TCCTCTGCCTCTTTC[C/T]GGTGGAACCTCAAGT | 83860 |
rs751891189 | snp | A/G | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964326 | ATTTACACCTAAAAC[A/G]AAGACTAAAACTAGC | 83860 |
rs751956054 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826046 | TGAAGTGTTACCTAT[A/T]TGTCTCAGGAAGTAT | 83860 |
rs751965803 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921441 | TACCTCCCCTCCCCC[A/G]TTTAAACTTTCTGAG | 83860 |
rs751966655 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850077 | GCTTTGCTTAAAATA[C/T]AGATCCTCGTATTTC | 83860 |
rs751967838 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934930 | ACCAAAGTCTGTACC[A/G]TCATGAAGCTTTGTC | 83860 |
rs751980581 | snp | C/G | 1.96169e-05 | 0.00313178 | missense | TAF3 | GRCh38.p7 | 10:8009148 | AGGCCGAAGACCCCA[C/G]CGCCGGCCCCCGCGC | 83860 |
rs751983301 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951881 | CACATCATACATGTC[G/T]CTATGATTGTAGGGT | 83860 |
rs751997253 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952543 | AGTCTTGCTGCAGTT[A/G]TGTGATACAACAGTA | 83860 |
rs752000699 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999369 | ACTATGGGCAATGTA[A/T]TTCTTTGAAAAGGCA | 83860 |
rs752078142 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867948 | TACAATAAATTAAGT[C/T]AGAGAAAAGAAAATA | 83860 |
rs752088722 | in-del | -/CTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893663 | GACTCTTGCCAGTTC[-/CTT]CTTATCATCCCTTTG | 83860 |
rs752123639 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945857 | CTTACTGTGAATTTT[C/G]CTTTTGTATTTGTTG | 83860 |
rs752123777 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821199 | GAGATTGTCAGGTTC[A/G]TTATTCCCACGTAAT | 83860 |
rs752131937 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916112 | TCCACCTCTTAACCC[A/G]AAGTGTTTGGTTTGG | 83860 |
rs752150705 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000375 | GCCTGTGTTGGCCTC[C/G]CAAAGTGCTGGGATT | 83860 |
rs752153835 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985486 | TATGAGAAAAAGGCT[A/G]TGTAACATCTGCTTT | 83860 |
rs752168913 | snp | A/G | 0.000304182 | 0.0123288 | missense | TAF3 | GRCh38.p7 | 10:8009229 | CTCGCCCAGGCCGCC[A/G]CGGGCCCTGCCCTGC | 83860 |
rs752180883 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833202 | CACATAATCTTTTCA[A/G]ATCTTTTGGGTAAAT | 83860 |
rs752186276 | snp | C/G | 1.85486e-05 | 0.00304531 | missense | TAF3 | GRCh38.p7 | 10:7965706 | GAGAGAGCGAGAGAA[C/G]AGAGAAAAAGAGAAG | 83860 |
rs752187253 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990821 | AGAGTCCTGCTCTGA[-/G]CCCTTATCCCATAGA | 83860 |
rs752202670 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992753 | TGAACGCATATTACC[A/G]ACTTCTAAAAAAGTT | 83860 |
rs752214267 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003709 | CTCCTCCCTTCTCTA[A/G]TTACATATGCCTACA | 83860 |
rs752234521 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941497 | AGAGTGAAGAGTTTC[A/C]GAGTTGAGTGGGCCG | 83860 |
rs752262581 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878985 | CGCTCACCTCAGCTT[C/T]CCAAAATGCTGGGAT | 83860 |
rs752279607 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820154 | AGAGTGTCCTTTGCC[C/T]GTGGCCCACCAATAG | 83860 |
rs752280232 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974140 | CTGAAACATACACAC[-/AC]ACACACACACACACA | 83860 |
rs752299414 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850411 | CTGGGAGCAGTGGCT[C/T]ATGCCTTTAATCCTA | 83860 |
rs752315138 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862689 | CTCTTCCCTCCTCCC[C/T]AGGGGGATCCCCAGG | 83860 |
rs752316652 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892467 | GCAATTGAAAACTTG[C/G]TGGGTTGCTCTAGTT | 83860 |
rs752336678 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935818 | TGATTCAGGAGAAAA[A/G]TGCAACTGGACCTGA | 83860 |
rs752339586 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923397 | GTTATGAAAATGGAC[C/T]CGTGTCCTTTGGGGT | 83860 |
rs752348621 | snp | C/T | 7.97162e-05 | 0.00631282 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014787 | CAAGCGGGGTCAGCC[C/T]GGGCTTCTTCCCTGG | 83860 |
rs752390308 | snp | C/T | 3.41513e-05 | 0.00413213 | intron-variant | TAF3 | GRCh38.p7 | 10:7824607 | GATTATTTTAATGGA[C/T]TTTTAATCCTCTTAG | 83860 |
rs752394259 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012665 | TTACGGAGGGTCAGA[G/T]ATGTAGTTGCCCACA | 83860 |
rs752404028 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979708 | TAAATGAAGTGAAAT[A/G]GATTACATTTTAAAT | 83860 |
rs752412164 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000332 | ATGTTGGCCAGGCTG[G/T]TCTCGAACTCCCAAC | 83860 |
rs752414487 | in-del | -/AAAAAGGAC | 0.000291475 | 0.0120687 | cds-indel | TAF3 | GRCh38.p7 | 10:7965614 | AAGGAGAAAGAAAAG[-/AAAAAGGAC]AAAAAGGAGAAGAAG | 83860 |
rs752463640 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966117 | CATATATTGAGAAAG[G/T]CAGCATCCATGTTTC | 83860 |
rs752498480 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971251 | TTAGACTGTGTTTCT[A/G]AATGGAAATAATGTA | 83860 |
rs752515046 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957186 | ACATGAGCATTAATA[C/G]CTATCCAGAACTACC | 83860 |
rs752537517 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855956 | CAAAAAAAAAATAAG[C/T]GTAATAGTTCTCTAC | 83860 |
rs752541604 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842418 | TCCAGCGTTGGCCTC[A/C]CAAAGTGCTGGGATT | 83860 |
rs752543551 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987526 | ATAAAGAAACAACAT[C/T]CTCATATATAGATTT | 83860 |
rs752571712 | snp | A/G | 1.86701e-05 | 0.00305528 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818667 | TGGCGGCGGGGCTGG[A/G]GAGCAGTGGCAGCAA | 83860 |
rs752575817 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928459 | TTTTAATGCATTTAT[A/G]GAAATCTTCAAATTG | 83860 |
rs752597054 | in-del | -/AGCGCG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957789 | TCTCACGCTCTCTCT[-/AGCGCG]CTCTCTCTCTCTCTC | 83860 |
rs752616584 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945126 | TGGGCAGCCTTTCCC[A/G]ATGCACAGTCTGAAG | 83860 |
rs752624977 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831867 | GGTTTCTTGGAAAGT[A/G]GTATTTCTTTTCTTT | 83860 |
rs752655034 | snp | A/G | 1.67464e-05 | 0.0028936 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965349 | TGTGAGGAAGGAGAA[A/G]GAGAAGCATAAAGAT | 83860 |
rs752657403 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886661 | ATACATCATAGCACA[C/T]AGCTGACATCCAGTA | 83860 |
rs752662427 | snp | C/T | 5.12667e-05 | 0.00506268 | intron-variant | TAF3 | GRCh38.p7 | 10:7977218 | AAAAACCATATTGAA[C/T]TTTAATGTGCTAACT | 83860 |
rs752663450 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848177 | AGCCAGATGTTAACT[G/T]GTACTAGCTATTCTT | 83860 |
rs752666640 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829748 | GTTTCTCTTCTATCC[C/G]CTCTTCCCCTACTGT | 83860 |
rs752667065 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868173 | GTTCAAGGGTCAACT[A/G]TATTGTTTGACAAGC | 83860 |
rs752694785 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958888 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 83860 |
rs752745072 | snp | A/T | 1.65765e-05 | 0.00287888 | missense | TAF3 | GRCh38.p7 | 10:7964180 | ATAAATACTCAAAAG[A/T]TCCCACCAATGCTTT | 83860 |
rs752759187 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846347 | GGTAATATAGAATAC[C/T]CATTATATTCTGTCC | 83860 |
rs752759956 | snp | C/G | 1.65963e-05 | 0.0028806 | missense | TAF3 | GRCh38.p7 | 10:7964075 | CCTGAAGCTGAAGAA[C/G]TGCCAGCCATGAAGC | 83860 |
rs752777263 | in-del | -/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828053 | GAAATACAATATACA[-/TT]AGTGAAGTCACGCTA | 83860 |
rs752795338 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960742 | ATTTTTATATTTTAT[C/T]TTTTCCTCCAATTTC | 83860 |
rs752796759 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974508 | CTTTCGAAACTGTGG[G/T]CAGGGATGAGATCAC | 83860 |
rs752821253 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834826 | AAAAAAATTTTTTTT[C/G]CTCATTCTGTCCTAT | 83860 |
rs752823968 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847051 | CAGCTTAAAATGGAC[A/C]AGAAAAAAATTGACA | 83860 |
rs752825626 | in-del | -/ATG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927722 | TGTGATGAAATAAAT[-/ATG]ATAATATATGTAGTT | 83860 |
rs752848926 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961805 | TTATTTCCTGTTTCT[A/G]TTCATCACTACATTT | 83860 |
rs752862096 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918724 | TTATATTCCGTAGAC[C/T]GTATCTCTGCCATAT | 83860 |
rs752886552 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972257 | TATTTTGGTGAGCAC[A/G]CAGATAAAGTTAATG | 83860 |
rs752892925 | snp | C/T | 0.000283369 | 0.0118998 | intron-variant | TAF3 | GRCh38.p7 | 10:8013688 | CTTTTTGTTTTTTTT[C/T]CCATTCCCTCCATTT | 83860 |
rs752906144 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925891 | TGATTAATTTAATTG[A/G]AGAATATGCTGGGAT | 83860 |
rs752913993 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835475 | CCACTTTTACCTGGA[C/T]CTTCTCTTCCCTTCA | 83860 |
rs752917101 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906536 | TTTAGGGTGGCTGTT[C/T]TATGAAACCTTAGAG | 83860 |
rs752917717 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892455 | CATAGTCAAAAAGCA[A/G]TTGAAAACTTGCTGG | 83860 |
rs752948066 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994167 | CGTGAATTCCTTCAT[A/G]TTGCCTACTGGGTTT | 83860 |
rs752965946 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997124 | AATATGTTTTTTCAT[C/T]GACCTGATTTTCCTC | 83860 |
rs752973634 | in-del | -/CC | 1.73833e-05 | 0.00294811 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014785 | ACCAAGCGGGGTCAG[-/CC]CGGGCTTCTTCCCTG | 83860 |
rs752982972 | snp | A/G | 3.31246e-05 | 0.00406955 | missense | TAF3 | GRCh38.p7 | 10:8013816 | TGATTGGGTGTGACG[A/G]CTGCGATGACTGGTA | 83860 |
rs753016781 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986761 | TTATTCACAGGGATC[C/T]ATAACTCACCCCAAG | 83860 |
rs753023163 | snp | C/G | 3.19923e-05 | 0.00399939 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009198 | CGTCAGCCCTGCGCC[C/G]GTGCCGCTGCCGCTG | 83860 |
rs753027423 | snp | A/G | 1.75078e-05 | 0.00295864 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965160 | AAAAGACAAGAACAA[A/G]GACAAAAGTAAGGAG | 83860 |
rs753037414 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953994 | ACAGGTGAATGAGTG[A/G]ATTAGTCCTAGTTAA | 83860 |
rs753039563 | snp | A/G | 1.80595e-05 | 0.0030049 | missense | TAF3 | GRCh38.p7 | 10:8009134 | CGCCCTCGCAGAACA[A/G]GCCGAAGACCCCACC | 83860 |
rs753071933 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958432 | GCAGTGAAAATAAGT[A/G]AACTACAGCTGCCTG | 83860 |
rs753079130 | snp | G/T | 1.66197e-05 | 0.00288263 | missense | TAF3 | GRCh38.p7 | 10:7964793 | CTAAGAGAATTTCAG[G/T]CCCGGAGTGTACTAC | 83860 |
rs753106113 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924210 | AAGTGTGAGGGAGAA[A/G]TGGAAAGCCAAAACT | 83860 |
rs753108099 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910274 | GTATGAAGTGTCTAA[G/T]AAAGATGTATAGTGT | 83860 |
rs753130383 | in-del | -/TGTGTGTGTGTGTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869248 | TCCTGACTTCTACCG[-/TGTGTGTGTGTGTC]TGTGTGTGTGTGTCT | 83860 |
rs753144792 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930178 | CGCTCCAACCTGGCA[A/G]CAGAGTAGCACCCTC | 83860 |
rs753146738 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942472 | TATATGACGTTGCTT[A/T]ATGTGAGTAACAGCA | 83860 |
rs753157598 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969637 | GGAACTGGATGGTTA[A/T]ACCTATATTCTTAAA | 83860 |
rs753172515 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868055 | ATCCTTGTCATCTTC[A/C]TGTTGAGTAGGCTGG | 83860 |
rs753212496 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845472 | GGGTGAACCCAAAGT[A/G]CATAAAATGCACTGA | 83860 |
rs753251377 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854433 | TGGAAGCTCTATGTG[A/C]TTTTTGGCTCTTAAG | 83860 |
rs753262720 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999309 | AAATTGACTGTCTAA[C/T]GTGGATGAGAGAGAC | 83860 |
rs753264774 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900003 | GACATGTTAGGCGGC[A/G]TCCACTCATATCCAA | 83860 |
rs753275313 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824306 | TTTGATTTGCTTTTC[-/A]CTTTGTTTCAGATGG | 83860 |
rs753284350 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839273 | TCTACCATCATACTT[C/T]ATATATTTTGTTATA | 83860 |
rs753325465 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924332 | TTCTCTGCTAGCATG[A/T]TTTGATTTTAGAAGG | 83860 |
rs753328896 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936063 | CGGTGTCCTGGACTA[C/G]TGTGATTGTATCGTA | 83860 |
rs753329147 | snp | A/C/T | 4.96819e-05 | 0.00498386 | missense | TAF3 | GRCh38.p7 | 10:7824411 | ACTATATTCACAACA[A/C/T]TGAGCCTGTCACCTT | 83860 |
rs753355309 | snp | C/T | 2.10104e-05 | 0.0032411 | missense | TAF3 | GRCh38.p7 | 10:8014638 | GTTTTCACGTGCAGG[C/T]CCTGTGTTGGAATCA | 83860 |
rs753356900 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833891 | TTTGGAGCGGTACCC[C/T]TTCAGCCGCTGCACA | 83860 |
rs753372148 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825840 | AATTCTTGCTTTCAG[G/T]TGTTTTTTTTTGGGT | 83860 |
rs753374707 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827578 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 83860 |
rs753377302 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920843 | CAATTTAGAAAGTTA[A/C]TAATTTTTTTAACAG | 83860 |
rs753386542 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911684 | AGTTTGTCTCATGTT[A/G]TGTATTTTAAAATTC | 83860 |
rs753412608 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880245 | CTTGTCTCGGAAAAA[A/G]TAAAAAATAAAACTC | 83860 |
rs753515587 | snp | C/T | 1.71255e-05 | 0.00292617 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964464 | ACGTTCCAAGAGCCC[C/T]AAGAGTCCCAAGAGC | 83860 |
rs753527160 | snp | C/T | 1.66026e-05 | 0.00288115 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964866 | ATCCACTCCTCTGCC[C/T]CTTTCCGGTGGAACC | 83860 |
rs753542232 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958980 | TCTACTAAAAATACA[C/T]ACACACAAAATTAGC | 83860 |
rs753549114 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899182 | GATTTTCGATCCTGG[A/G]CCTCACCTACATCCT | 83860 |
rs753644427 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873537 | TTAGAATAGTTTAGT[A/G]GAACTGGAACAAAAT | 83860 |
rs753651493 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946037 | CTGACCCTGACTGTC[C/T]TCCTGCCTTGGCCTC | 83860 |
rs753687745 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960218 | CACTTTCAGAATACC[A/C]TAAAGCTGTCTTCTT | 83860 |
rs753695849 | snp | C/T | 1.73902e-05 | 0.0029487 | missense | TAF3 | GRCh38.p7 | 10:7964526 | CTGTGAGACCTGAAA[C/T]GCCCAACAGGACTCC | 83860 |
rs753698512 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963232 | AATCCATACTAAGTC[C/T]TATAATAATCCATCT | 83860 |
rs753708500 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947294 | CCCACCGCAGGCCGG[A/C]TAGTGCGGTTAAGAG | 83860 |
rs753724718 | snp | C/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993163 | TATTTTTAATCCACA[C/G/T]TCCTACGCTCCTCCT | 83860 |
rs753752913 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821392 | CACTTACTGAGCATC[A/G]CTTACGAACCAACCC | 83860 |
rs753755051 | in-del | -/ACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939580 | ATAGAAGAAAACTAC[-/ACACAC]ACACACACACACACA | 83860 |
rs753762506 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993970 | CAGTGATGAGCATAG[A/G]GTTTTGGAAAGGGGA | 83860 |
rs753765553 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905024 | ACGTTTCTTGTATCC[A/G]TGTCTCTTTGAGAAG | 83860 |
rs753787494 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959166 | CACACACACACACAA[-/AA]AAAGTTTCAGGCTTT | 83860 |
rs753789559 | snp | G/T | 1.70098e-05 | 0.00291627 | intron-variant | TAF3 | GRCh38.p7 | 10:8013680 | TCTGGCCTCTTTTTG[G/T]TTTTTTTCCCATTCC | 83860 |
rs753789852 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864099 | TATTATTACCAGAGT[C/T]TGTAGTTTTCCTTAG | 83860 |
rs753798594 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941683 | TGTGTCTGTTAGGTC[A/G]GGAAAATAGTAAGTT | 83860 |
rs753798905 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874871 | AACTAAAGAAATTAT[A/G]TATTGAGCTCGGGTT | 83860 |
rs753800312 | snp | A/T | 1.66707e-05 | 0.00288705 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965565 | TTTGTTGCCAGTGCT[A/T]CCGGAAAAACTGTTT | 83860 |
rs753817378 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885503 | TGCATTTTGTCTGCC[C/G]CATTTCCCTCCTCAC | 83860 |
rs753822140 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012869 | TATCCCTTACAAAAT[A/G]AACCGGATGCAATAA | 83860 |
rs753855666 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848389 | TGGTAAAGGAGAAAA[A/G]CTCCTTTTTCATTTC | 83860 |
rs753875391 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997423 | ATCCAACTTGTGTTT[C/G]CTGCTAACCCTGGAG | 83860 |
rs753875564 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866475 | CATCGTGACCAGCAA[A/G]GAAGAGTGTGCTAGA | 83860 |
rs753885610 | snp | C/T | 1.71437e-05 | 0.00292772 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965103 | AAAGGAACTAAAGAC[C/T]AAAATGAAAAAGAAA | 83860 |
rs753891622 | in-del | -/AAGTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831987 | CAATGTGGAATAATT[-/AAGTC]AAGCTAGTTAACATA | 83860 |
rs753893941 | snp | A/C | 1.84759e-05 | 0.00303935 | missense | TAF3 | GRCh38.p7 | 10:7965676 | GAAGAAGGAGAAGGA[A/C]AGAGAGAAAGAGAAG | 83860 |
rs753902139 | snp | C/T | 1.67388e-05 | 0.00289294 | missense | TAF3 | GRCh38.p7 | 10:7964993 | CCTTATATCTCTTCT[C/T]CGTCAGTGTCTCCTC | 83860 |
rs753911412 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995646 | CCCCTAATTACTTCA[C/T]GCAATTTGTTTCATT | 83860 |
rs753913153 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919623 | AATGCTCAAGTCCCT[G/T]ATGTAAAATGGTATA | 83860 |
rs753919616 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962752 | TTTGACCTGCTGTAG[C/T]ACTTTATCTGTCTGT | 83860 |
rs753934310 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864994 | AAAGGATCCCTGCAC[A/C]ATTTGTTGAATTCCA | 83860 |
rs753936655 | in-del | -/TAGGC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820940 | GTATACCGTTAGTGA[-/TAGGC]TAGGCTAGGCTAGGC | 83860 |
rs753971054 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907925 | AACCAGCAGGAGTCG[A/T]TGGGGACTGAATCTG | 83860 |
rs753986585 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950116 | GCAGATGTGGTTCCC[A/G]TATCAGTGAAGCTTT | 83860 |
rs754000595 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010655 | CTTACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 83860 |
rs754011972 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835699 | GCTCTTCTCGGGTTG[A/G]CCTGCCGGGCTTTCC | 83860 |
rs754020575 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854736 | GTTTCTGTGTGTATT[C/T]GAAGGGGGCTTCCTG | 83860 |
rs754046333 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824843 | TTCAACAGCCCTATT[A/G]TATGAGAATGGGATA | 83860 |
rs754056888 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906865 | TGGGACTGCAGGCGT[A/G]CACCACCATGCCCAG | 83860 |
rs754072489 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983659 | TGAAACATTTCATAG[A/G]TATTTTGCCTACGTT | 83860 |
rs754104655 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866377 | ACGTAGGGGCCTGTG[A/G]TGGTGGCTGACCACG | 83860 |
rs754145507 | snp | C/T | 1.96767e-05 | 0.00313655 | intron-variant | TAF3 | GRCh38.p7 | 10:8009338 | CCTACGTGGTGCGTA[C/T]CTGCCGCCCGCGCGG | 83860 |
rs754154217 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974635 | ATAATGGGAAAACTG[A/G]GACATGAGGACATTG | 83860 |
rs754161328 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001163 | AGCTGTCTAATGTTG[C/T]CTCAGGATACATTTC | 83860 |
rs754178044 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816952 | TATAAATACAAAATA[C/T]ATAGTAAATTGGCAA | 83860 |
rs754207147 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942603 | CGAGTCCTAGGACAT[G/T]GCTGACTGAGAAAAT | 83860 |
rs754238098 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932185 | GTGAACATGCTACCT[C/T]TATCAGTCAGTGTGA | 83860 |
rs754238431 | snp | C/T | 1.65767e-05 | 0.00287891 | missense | TAF3 | GRCh38.p7 | 10:7964163 | GAGAGCCACTCAGCT[C/T]AATAAATACTCAAAA | 83860 |
rs754249517 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999592 | ATCTCAAGTAGCTGG[G/T]ATTATAAGTGGATAC | 83860 |
rs754259858 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931442 | GATTTTCCATGGATA[C/T]TTGAAATTCTTGTTA | 83860 |
rs754260309 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829130 | CTTGGTAAAGATACT[C/G]TGAGGTTGCCACTTT | 83860 |
rs754261495 | in-del | -/TTCCTTCCAG | 3.34264e-05 | 0.00408804 | frameshift-variant | TAF3 | GRCh38.p7 | 10:7965373 | AAAGATAAGAAGAAA[-/TTCCTTCCAG]GATAGAGAGAAAGGC | 83860 |
rs754261647 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870584 | GTTAGTGAAAAATGG[C/T]GGTCTGTTGTTGAAG | 83860 |
rs754278215 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895319 | TCCTTTGCTGTATCT[C/G]TACAGCAATGGCTTC | 83860 |
rs754279721 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819687 | TCTTGTTGATGTGAA[A/G]CATTGTATGTGTGTT | 83860 |
rs754316004 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947542 | TGCAGTGATCAGAGA[C/T]GGCTTCACTGAGGGG | 83860 |
rs754324049 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876304 | AATTATTACCTGAAA[A/G]CAATACTTTAGCTTC | 83860 |
rs754349316 | in-del | -/C | 1.658e-05 | 0.00287919 | intron-variant | TAF3 | GRCh38.p7 | 10:8013868 | GCCCTGCCGGCCACA[-/C]TCATTAGGCAGCATC | 83860 |
rs754412887 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975603 | TAAAAGGGTTGGGGC[A/G]AGATAAGTTGATAAT | 83860 |
rs754416480 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889751 | AAATAGCCTCGTCTT[C/G]TGTCTTGTTTCTTGT | 83860 |
rs754424008 | in-del | -/CACTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979880 | GGGCCAAATCCAGGC[-/CACTG]CCTGTTTTCTGTGAC | 83860 |
rs754434967 | snp | A/G | 3.3206e-05 | 0.00407455 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964065 | ACTGGATAGTCCTGA[A/G]GCTGAAGAACTGCCA | 83860 |
rs754435387 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847824 | CCAGGCTGGAGTGCA[C/T]TGGTGCAATCTGGGC | 83860 |
rs754442550 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893794 | CAATATTTTATCAGC[C/T]ATTTTCTTATCTTTA | 83860 |
rs754448416 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860315 | AAGAAAAATTCAAGA[A/G]ATGAATTATTAAGCG | 83860 |
rs754455714 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902701 | TATAATTAATGAGTA[A/G]TAGGCTGAGTGATAC | 83860 |
rs754481070 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817660 | ATTTATCCCTAAATC[C/T]GATTTCTGGCAATAC | 83860 |
rs754488176 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914175 | AGGTGTGATGATGGC[A/G]ATGTGGTTATACATA | 83860 |
rs754562620 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857126 | TGTTAATGAGGAAGA[-/C]AAAAGTGAAACAACA | 83860 |
rs754571654 | snp | C/T | 3.33639e-05 | 0.00408422 | missense | TAF3 | GRCh38.p7 | 10:7965567 | TGTTGCCAGTGCTTC[C/T]GGAAAAACTGTTTGA | 83860 |
rs754573761 | snp | A/G | 6.57311e-05 | 0.00573247 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014777 | GGGGCTGGACCAAGC[A/G]GGGTCAGCCCGGGCT | 83860 |
rs754587288 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010391 | TAGAGACGCATGGTG[G/T]TACTGAAATCTCACA | 83860 |
rs754596841 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877939 | ATCTCAAATACATTG[C/G]AGCTAATGTTTCTGT | 83860 |
rs754607401 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976638 | CGAATTCCTGACCTC[-/A]ATGACGCCTGCCTCA | 83860 |
rs754609602 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837226 | AATTTAGCTGGACAT[A/G]GTGGCATGGGCCTGT | 83860 |
rs754613904 | snp | C/T | 1.66029e-05 | 0.00288117 | missense | TAF3 | GRCh38.p7 | 10:7964867 | TCCACTCCTCTGCCT[C/T]TTTCCGGTGGAACCT | 83860 |
rs754617528 | snp | A/G | 1.69421e-05 | 0.00291046 | intron-variant | TAF3 | GRCh38.p7 | 10:7824268 | AATATTTAAAAATAT[A/G]TTCGTGGGATTTCTT | 83860 |
rs754620206 | snp | C/T | | | missense | TAF3 | GRCh38.p7 | 10:7964391 | CCCAGTCACCAGCAA[C/T]GGTCGGAAGTCCTAT | 83860 |
rs754642462 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011533 | CTTCCACCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 83860 |
rs754665439 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959494 | TAGGAACTTGAAAAA[C/T]AAAAGTGAAAATAAA | 83860 |
rs754695208 | in-del | -/CC | 1.65636e-05 | 0.00287776 | frameshift-variant | TAF3 | GRCh38.p7 | 10:7824524 | AGAAAAGAATACATT[-/CC]TGATTACCTGCCACC | 83860 |
rs754695456 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973755 | AGATAACACAGAAAG[A/G]TGAGGAAGTCTTAAA | 83860 |
rs754696609 | snp | A/G | 1.65433e-05 | 0.002876 | missense | TAF3 | GRCh38.p7 | 10:8014644 | ACGTGCAGGCCCTGT[A/G]TTGGAATCATGACTG | 83860 |
rs754697400 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987377 | TCAGCAGCTTATCCC[C/G]TCCCCTCTAACAGAT | 83860 |
rs754703490 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968729 | TCACACATCTAGTAA[A/G]TGATTGAACAGGAGC | 83860 |
rs754733461 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921668 | TCACCACCAAAGTTT[C/G]AAAATGATTACTACA | 83860 |
rs754742000 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840995 | GCTGGGATTACAGGC[A/C]CACGCTGCCACACCT | 83860 |
rs754755394 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985123 | TCCACGTCACTGCAG[G/T]ACTGCTGTCATTTAG | 83860 |
rs754758576 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879345 | TAATGAAACGTAACT[A/G]TGGTTTCAGTTGGTA | 83860 |
rs754777663 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924141 | TTTGAATACATCATT[C/T]TTAGACAGTGTTTGT | 83860 |
rs754784664 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895642 | GAGTCTTGGGAAATT[A/G]GGGCATGATTCTAAT | 83860 |
rs754788376 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829402 | TTTCTGGATCCCATC[C/T]AGGATATCATATTGT | 83860 |
rs754793049 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014314 | TGTTATCTTTAAAAT[A/G]TCAGATACAAAAAAG | 83860 |
rs754802626 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882068 | AGAGTTGATTTGTCT[A/G]TGAGTTTTCATGAAC | 83860 |
rs754853364 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830736 | TGATCCGCCAGCCTC[G/T]GCCTCCCAAAGTGCT | 83860 |
rs754906442 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842394 | TGAACTGCAAGGCTC[A/G]ACCAGTCTTCCAGCG | 83860 |
rs754911159 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003390 | TAGCTCTGTTTACCC[A/C]TTACTGGCTTACATA | 83860 |
rs754938560 | in-del | -/AAAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969144 | CTGTCTCTCCAAAAC[-/AAAC]AAACAAACAAACAAA | 83860 |
rs754943459 | snp | C/T | 1.71882e-05 | 0.00293152 | missense | TAF3 | GRCh38.p7 | 10:7964471 | AAGAGCCCCAAGAGT[C/T]CCAAGAGCCCCAAGG | 83860 |
rs754951147 | snp | G/T | 1.85827e-05 | 0.00304811 | missense | TAF3 | GRCh38.p7 | 10:7965699 | AAGAGAAGAGAGAGC[G/T]AGAGAAGAGAGAAAA | 83860 |
rs754969554 | in-del | -/TATG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957658 | TATTTGTTTCTCACA[-/TATG]TACAGAAGAGTCCTT | 83860 |
rs754974831 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930052 | ACCAAAAACAAAATA[A/G]CAAAGTGGGGTGGCA | 83860 |
rs754986155 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957062 | AATACATTCTCACAC[A/G]TGGGAAAAGCAAATC | 83860 |
rs755020548 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870882 | CTTACCTTTCTTGAA[A/G]CTCAGAGTTTCTTGT | 83860 |
rs755037121 | in-del | -/GGTCCCTCGACCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848542 | CAGCAACCCCTTCCA[-/GGTCCCTCGACCT]GGTCCCTCGACCTGG | 83860 |
rs755049298 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973013 | AGCAGTAGGGTGAAC[A/G]GGGGATGAATTTGGT | 83860 |
rs755056660 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005652 | CTGCTTACCTCTCAG[A/G]GTTCCTGCTTTTCCC | 83860 |
rs755084677 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887776 | AGATCCCTGGTTATA[C/T]CTTTTGGTTTATTAA | 83860 |
rs755087690 | in-del | -/CTAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843630 | TGTTGTGTGTCTCCC[-/CTAT]CTCTTTCTCACTCTT | 83860 |
rs755093578 | snp | C/T | 1.95616e-05 | 0.00312737 | intron-variant | TAF3 | GRCh38.p7 | 10:8009342 | CGTGGTGCGTACCTG[C/T]CGCCCGCGCGGTTAG | 83860 |
rs755131100 | snp | A/G | 5.24498e-05 | 0.00512076 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965142 | GAGAGATAGGGAGAG[A/G]GAAAAAGACAAGAAC | 83860 |
rs755138214 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874987 | CATTTGTGCTTCTTA[A/G]TCCTTCAAAATGTGC | 83860 |
rs755138777 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942733 | TCCCAAGTGGGCAGC[C/T]GAGGCGTGTGGGCAC | 83860 |
rs755144257 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993087 | TCAAAAATATCTTCA[A/G]CAGTTTAACCAGGAT | 83860 |
rs755162406 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948719 | GATAGATACATAACA[A/G]CCAAAAGCTTAAATA | 83860 |
rs755174478 | in-del | -/TCTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918741 | TATCTCTGCCATATT[-/TCTA]TCTGTTACCTGGGAA | 83860 |
rs755180561 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007163 | GTAGGATGATGGACA[A/G]AAACCTTTGGCTTAC | 83860 |
rs755185594 | snp | A/G | 1.67427e-05 | 0.00289328 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964995 | TTATATCTCTTCTCC[A/G]TCAGTGTCTCCTCCC | 83860 |
rs755199184 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994050 | CTCTTTCTCTGCTCC[C/G]CCTACCCCTTCTTCT | 83860 |
rs755200959 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834727 | ATAAAATTAGAATAT[C/T]CCATAATTATTCATT | 83860 |
rs755233760 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980504 | CTCCTCCTGATAGTG[G/T]TAAAATTCAAGATGA | 83860 |
rs755248488 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007200 | CATGGAATACAATAT[A/G]GTAATTAGAATAAAT | 83860 |
rs755287659 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878853 | CTGTCTCAGCCTCCT[A/G]AGTAGCTGGGACCAC | 83860 |
rs755317020 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905387 | ATTATTAAGTATTTT[C/G]TCTCTTTTAGACAAA | 83860 |
rs755318102 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896412 | CAAGGGAGAAGGACA[A/G]GAGGAGGCTTTTCAA | 83860 |
rs755373118 | snp | C/T | 1.79326e-05 | 0.00299432 | intron-variant | TAF3 | GRCh38.p7 | 10:8009053 | ATCCTGTTTTGACTT[C/T]TACCTTCTCTTCTTT | 83860 |
rs755391089 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910138 | TTGAGTCCAAGGATG[C/T]ACAGCCTGTAGGTAG | 83860 |
rs755420792 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996927 | TCAAACTCCTGAGCT[C/T]ACACAGTCTGCCTGC | 83860 |
rs755444176 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897080 | CCTCATGCTTTGAAT[C/T]CCCAACTTCTTCTTC | 83860 |
rs755474575 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864190 | CCATTATAACATCAT[-/AC]AGAGTAGTTTCACTG | 83860 |
rs755489250 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985608 | CTTTTCTACAGCTTC[G/T]TGTTAAGACCATTAG | 83860 |
rs755504468 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844095 | TTCATAATTTAGCGT[C/T]TCTGGAACTTTGTGA | 83860 |
rs755527984 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941203 | AATCCAGCAAGCTGA[A/G]TGACCACGTTTAGCC | 83860 |
rs755529254 | snp | A/G | 0.000226526 | 0.0106401 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818897 | ACCGGGCTGGGTGCG[A/G]GAGGGCTGCCCCGGC | 83860 |
rs755536602 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857339 | CCCTATCACAGGTAC[A/G]TAGTTTTATCCGATT | 83860 |
rs755543745 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011115 | TGCTGTGACTACCAA[-/C]TCTGCAGACTGTGAT | 83860 |
rs755555379 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868023 | TTGAGTGGAAGTGGG[A/T]CACCATAAAGTTGTT | 83860 |
rs755571839 | in-del | -/ACATACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974130 | GAGATTCCTTCTGAA[-/ACATACAC]ACACACACACACACA | 83860 |
rs755573397 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971601 | GGAATGCATGAAAGA[A/G]TTCCAAGATAGAATT | 83860 |
rs755595838 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850413 | GGGAGCAGTGGCTCA[C/T]GCCTTTAATCCTAGC | 83860 |
rs755599791 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935154 | TGCTGGTGCGCGCCT[A/G/T]TAATCCCAGCTACTC | 83860 |
rs755653063 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923482 | CTTTTATTCTTCCAG[C/T]ATGTGCCATATCTTT | 83860 |
rs755654436 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892501 | CTTCTGTTACAATAA[A/G]ATGTGATGATTTTTT | 83860 |
rs755658724 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011693 | GCAACATCACCCCCA[A/G]ATGGGTTGATCAGGA | 83860 |
rs755667481 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977074 | TCATGATGCCAGGTA[A/G]CCTTCAGTTGTACAG | 83860 |
rs755674665 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871798 | CCTGAGAAGTAAAAA[A/T]TCATACATTTAATGA | 83860 |
rs755676613 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897454 | GAGTTTTCTCTCTAG[C/G]AAATTTAGATTCTTC | 83860 |
rs755693344 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862055 | GGGTCACTGAGCTTT[C/G]TGCTACACATGCAGT | 83860 |
rs755696128 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916135 | TGGTTTGGATGCTAC[C/G]CAGGAGTGACTTGTT | 83860 |
rs755702869 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839190 | CTGGGTCAGCTCATG[C/T]TGGCATGGAGTTCTC | 83860 |
rs755705731 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880163 | AGAATCACCTGAGCC[C/T]GGGAGTTCTAGGCTG | 83860 |
rs755711227 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003979 | TATCTGTTAACATAT[-/A]ATGGGTTCATTGTCG | 83860 |
rs755711782 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012667 | ACGGAGGGTCAGAGA[A/T]GTAGTTGCCCACAGA | 83860 |
rs755726953 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985865 | CTTGGCTCACTGCAG[C/T]CTCCGCCTCCTGGGT | 83860 |
rs755738395 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826192 | ATTTAGGTGCTCTGG[A/T]TCTTAGCTGCAGTGG | 83860 |
rs755748703 | snp | C/T | 1.66183e-05 | 0.00288251 | missense | TAF3 | GRCh38.p7 | 10:7964667 | TGGTAGCAGATAAAA[C/T]GATTGAGGCCTCTAT | 83860 |
rs755765912 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952767 | GTATGAATTGTCATT[C/G]CCTAATTGTCTTGTC | 83860 |
rs755767216 | snp | C/T | 1.66217e-05 | 0.0028828 | missense | TAF3 | GRCh38.p7 | 10:7964790 | GCCCTAAGAGAATTT[C/T]AGGCCCGGAGTGTAC | 83860 |
rs755794075 | snp | C/T | 1.85118e-05 | 0.0030423 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818760 | CTCGGTGGCGCAGAT[C/T]TGCCAGGCGCTGGGC | 83860 |
rs755812574 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820496 | TTCACTGATACTTCT[A/G/T]TTACTCTTCTTCTTT | 83860 |
rs755824688 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838125 | GAATTAACCTGCCTC[A/G]TGTTGCATTGGGAAT | 83860 |
rs755836593 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957209 | GAACTACCTTTCCTT[A/G]GTTAAATACCCACTG | 83860 |
rs755874603 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830874 | GGTTGTTTGATCTGC[A/T]GAGTGCCCCACAGTT | 83860 |
rs755878172 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914804 | CACTTGTCATTAGTC[C/T]TGCAGGTAGAGTGAA | 83860 |
rs755887883 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860899 | CTGCCTCCTGGGTTC[A/G]AGCAATTCTCTGCTT | 83860 |
rs755893436 | in-del | -/TACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939577 | GAAATAGAAGAAAAC[-/TACACA]CACACACACACACAC | 83860 |
rs755899504 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914038 | ATCAACCAATTGCAA[C/T]GTGGTCCTCTTTTAG | 83860 |
rs755925404 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885699 | CACACAGTCTTCATT[A/G]TCTCCCAAATAATCA | 83860 |
rs755928050 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004381 | GGTAAATATTGACAG[A/G]TATAGTGCACATTTT | 83860 |
rs755952283 | in-del | -/TCTGAGGCCACTGCATT | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006905 | TTCTCACTACAACCC[-/TCTGAGGCCACTGCATT]TCTTTTCACTTTGTT | 83860 |
rs755970628 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001837 | TCAATTGCACATGCG[-/T]TAATTATTGCATAGT | 83860 |
rs755972756 | snp | G/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820300 | CTGTGTATGTCTCTT[G/T]CCCCTCTCCAGGAGA | 83860 |
rs755979290 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881493 | CACATACACACAAAC[-/AC]ACACACACACACACA | 83860 |
rs756027357 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958910 | GAGGCTGAGGTGGGC[A/G]GATCACAAGGTCAGG | 83860 |
rs756029353 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945265 | TTGCCTAGTGAGTTT[C/T]TGTTTGTGTGCCATT | 83860 |
rs756030137 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831916 | TTAATTATAAAATTT[C/G]AGGTTACATTTGTAT | 83860 |
rs756040665 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990367 | GGCAGAATGGCTGGC[C/T]ACCTTTTTATTGTTT | 83860 |
rs756081495 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945920 | ATAGAGAAACCTTGT[A/C]TTTTGTTTGTTAACC | 83860 |
rs756147680 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918725 | TATATTCCGTAGACC[A/G]TATCTCTGCCATATT | 83860 |
rs756150067 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978310 | GTGGTTCATTTCATC[C/T]TAAAAGTTACATGTA | 83860 |
rs756170667 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873406 | GTGATTTACTTTGAC[A/G]ATAAAAATGTAGGGT | 83860 |
rs756207471 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961881 | TAAAAATAGGGTCTC[A/G]CTCTGTCGCCCAGGC | 83860 |
rs756207866 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875201 | TTGTTCCTCCTCGAT[A/G]TTTTTTTTCTGTCTC | 83860 |
rs756211474 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924409 | ACTTAGTAAGTGTCT[A/G]TGCTTGCCTTTTCAT | 83860 |
rs756214417 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994191 | TGGGTTTCGACACAA[C/T]CTCATTTGTGTTGGA | 83860 |
rs756298130 | in-del | -/TGAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993720 | TAGGCATGGAATGTC[-/TGAT]TGTCACATTCTTAGT | 83860 |
rs756301349 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947473 | TTAGGTAAGGGAGTG[C/T]AGTGGCAATGAGGCC | 83860 |
rs756303593 | snp | C/T | 3.32132e-05 | 0.00407499 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964890 | TGGAACCTCAAGTTC[C/T]GATAACTCATGGACA | 83860 |
rs756305633 | snp | C/T | 2.01949e-05 | 0.00317758 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009327 | GACGGTCAGCACCTA[C/T]GTGGTGCGTACCTGC | 83860 |
rs756356239 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868812 | ATTATGATTTTGTTA[C/T]CTGTTTTACTTATAA | 83860 |
rs756359374 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902507 | GCGTGTGGTTGTTTT[C/G]TCATGACGAAACTCA | 83860 |
rs756410188 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937548 | ATGGTTCATTTTTTT[G/T]TTGTTGAGTTTTAAA | 83860 |
rs756410944 | in-del | -/TTAGTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916086 | TGGATTGTAAATGTT[-/TTAGTG]TTAGTGTAGCTCCAC | 83860 |
rs756422852 | in-del | -/GTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904434 | TGCCATGAGAAAGAC[-/GTT]GTCTGTCCAGTTCAT | 83860 |
rs756423664 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941525 | CCGTGTAGTAATCAA[A/G]GTAAATGTGCTCTTT | 83860 |
rs756426478 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907404 | GCATTTAGATTTATT[C/T]TTTTGTATTTAATTT | 83860 |
rs756476667 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930190 | GCAACAGAGTAGCAC[C/T]CTCTCAAAACAAACA | 83860 |
rs756497795 | snp | G/T | 1.66313e-05 | 0.00288364 | missense | TAF3 | GRCh38.p7 | 10:7964040 | ATGAGAATTTCCTGG[G/T]CAAGAGACCACTGGA | 83860 |
rs756531660 | in-del | -/TC | 1.82693e-05 | 0.00302231 | utr-variant-5-prime, frameshift-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818696 | AGGGCTGCGGTGGCG[-/TC]TCCACGCAGCGGGAT | 83860 |
rs756540196 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827479 | TCATGAGACCTCATC[G/T]CTACTAAAAATAAAA | 83860 |
rs756545213 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935048 | TCTGGAGGCCAAGGA[C/T]GGTGGATCACTTGAG | 83860 |
rs756559379 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986933 | AACTGCTTCAAAATA[C/T]GTAACCTAGAAAGCA | 83860 |
rs756573526 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898657 | ATGTCTGAAGCTCTT[C/G]AAGCACTGGGTTCTT | 83860 |
rs756578072 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887830 | CACTTAAAAAAAAAA[A/G]CACCAAAACAAATTA | 83860 |
rs756584575 | snp | G/T | 2.55073e-05 | 0.00357113 | intron-variant | TAF3 | GRCh38.p7 | 10:7963899 | TATTTATTTTTTTCT[G/T]CCTTTTTCTTCCTTT | 83860 |
rs756590498 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007227 | AAATAATATAGATCT[C/G]TATGTGTCAGCATGG | 83860 |
rs756598784 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974621 | GCATGAGAAGACCTA[C/T]AATGGGAAAACTGGG | 83860 |
rs756618409 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854725 | AATATGTGCATGTTT[C/G]TGTGTGTATTCGAAG | 83860 |
rs756637417 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942503 | GTGTAACACAGTCTT[C/G]CTGATTTACCCATAA | 83860 |
rs756658461 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006376 | GTGAAACTCCATCTC[-/A]AAAAAAAAAAAACCT | 83860 |
rs756662638 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931371 | GCCATATTTATTTTC[C/G]TGCTGACCCTGAAAT | 83860 |
rs756677664 | snp | A/G | 1.67267e-05 | 0.0028919 | missense | TAF3 | GRCh38.p7 | 10:7964984 | CCCAACTTTCCTTAT[A/G]TCTCTTCTCCGTCAG | 83860 |
rs756677770 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846208 | GTGATCTGCCCGCCT[C/T]GGCCTCCCGAAGTGC | 83860 |
rs756684991 | in-del | -/GAAAGA | 0.000364783 | 0.0135003 | cds-indel | TAF3 | GRCh38.p7 | 10:7965186 | GGAGAAGGATAAAGT[-/GAAAGA]GAAAGAGAAAGAGAA | 83860 |
rs756686597 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858878 | TGTGCGTGTGTGCAT[A/G]TGAACATGTGAATGT | 83860 |
rs756701999 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858807 | GTACATTATAGGCTC[-/TG]TGTGTGTGTGTGTGT | 83860 |
rs756704158 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845660 | ATCAGATTTAGAGTG[-/AA]AAGGTGAGAGGTCTC | 83860 |
rs756724687 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845478 | ACCCAAAGTGCATAA[A/G]ATGCACTGAAATGAT | 83860 |
rs756748384 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924466 | TTTGCTTGTTAAGTC[C/T]GGGGATCTGCCTATC | 83860 |
rs756757149 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952894 | TTACATTATAGACAG[A/G]ACAATTTTAAAATAT | 83860 |
rs756757489 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967021 | TAAAGCAGATCCATA[C/T]ACCTTGTTTTCTCCT | 83860 |
rs756761658 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839321 | CCTCTGTAACTTACC[C/T]AGGTCTTGCTTTCTC | 83860 |
rs756767995 | snp | A/G | 1.66233e-05 | 0.00288295 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964647 | GAATCAGCCGAAAAA[A/G]GCTGTGGTAGCAGAT | 83860 |
rs756779096 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894060 | TGCACATTTTGTTTT[A/G]TTAGTACTAAAATTA | 83860 |
rs756809749 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911740 | TCAGAAAAATTTTAC[A/G]TAACAAATAAGCAGT | 83860 |
rs756822065 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952752 | TTGATTGGTTGTAAT[A/G]TATGAATTGTCATTG | 83860 |
rs756826872 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014533 | CTTGACTTTGATTTC[A/G]GGTAAACATGTCATA | 83860 |
rs756837533 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829204 | AACAGTTTTGATTTA[C/G]AGAAAAAATTGAGAA | 83860 |
rs756856088 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858937 | AGCGTCTTCTGGGCT[C/G]TATTCATATGTCATC | 83860 |
rs756857077 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000651 | AGGCATGGTGGCACG[C/T]ACCTGTAGTCCCAGC | 83860 |
rs756857672 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982076 | ATTTAGCCAAATGAC[A/T]TTCAACAGAGTGAAG | 83860 |
rs756878713 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987248 | TTGAGCCTGGGAAAT[C/T]GAGGCTACAGTGAGT | 83860 |
rs756881657 | in-del | -/TCTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897659 | TTCTCTCTCTCTCTC[-/TCTT]TCTTTCTTTCTTTCT | 83860 |
rs756892870 | snp | A/G | 1.70918e-05 | 0.00292329 | intron-variant | TAF3 | GRCh38.p7 | 10:7977363 | GGTGAAACAAATGAA[A/G]TTTAACCTTCTCTAC | 83860 |
rs756900666 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942674 | CAAACACAGATCCCA[A/G]GAAGCGCTGGGGAAT | 83860 |
rs756923320 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912358 | TTCTGCGTTGGCCCC[A/G]CAAAGCGCTGGAATT | 83860 |
rs756954476 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869621 | CGTTTTCTCATAATT[G/T]CCTTAAGAGAAATTC | 83860 |
rs756957131 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827631 | CTAAAGATACAAATA[C/T]TAGCTGGGCGTGGTG | 83860 |
rs756969594 | in-del | -/TTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874139 | AAAATATACCTCTTA[-/TTG]TTTTATCTATCTGAA | 83860 |
rs756978998 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833320 | TAAATTCCCACCAAC[A/C]GTGTACAAGGATTCC | 83860 |
rs756980915 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820479 | TGTTTTGAATGCTTG[A/G]TTTCACTGATACTTC | 83860 |
rs757032550 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862904 | AGTATTGTTCCATTA[C/T]GTGTATATGCCACAA | 83860 |
rs757039512 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899230 | CCTCGATCTGGAGCC[A/G]TTCTCATTCGGTCCC | 83860 |
rs757070459 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992923 | TTCAAAACTTAATAT[A/C]ATTTCACCTCTATAT | 83860 |
rs757078511 | snp | A/G | 1.66048e-05 | 0.00288134 | intron-variant | TAF3 | GRCh38.p7 | 10:8013700 | TTTCCCATTCCCTCC[A/G]TTTTTGCCGCTTCCG | 83860 |
rs757082316 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873566 | ATGTCATTTTCTAAA[C/T]CTAAGTTTCTTTGGT | 83860 |
rs757083814 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917356 | AAAACATTTCAGGCA[C/T]GAGGAACAGCAAGTA | 83860 |
rs757089222 | snp | A/G | 3.33517e-05 | 0.00408347 | missense | TAF3 | GRCh38.p7 | 10:7965408 | AAGATAAAGATAAGA[A/G]AGAGAAAGAAAAAGT | 83860 |
rs757096570 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891507 | AGGCATGGTTAAGTC[C/T]TATGGCATACCACTT | 83860 |
rs757123796 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980242 | GAAATTAGGAAAAAC[A/G]AAAAAGCTTTACAGG | 83860 |
rs757145888 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978561 | TGCAGCAAAAATCCT[A/G]TGGATTCAGTGCTTT | 83860 |
rs757188885 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923525 | TCTCAGAAAGAGCTT[A/C]ATCACTTTTTTCTGG | 83860 |
rs757196773 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005934 | CTGGCCCTGCCATGT[A/G]GTAGTAACCTGTGTT | 83860 |
rs757212110 | snp | A/G | 3.44911e-05 | 0.00415263 | missense | TAF3 | GRCh38.p7 | 10:7965195 | ATAAAGTGAAAGAGA[A/G]AGAGAAAGACAAGGA | 83860 |
rs757223641 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950198 | GACTCCTTATTTTGG[A/G]GATGTAGAATGACCA | 83860 |
rs757231690 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012730 | TGCCTTTGTAGAGTT[A/G]CCTTAAAGGAAGCCC | 83860 |
rs757238950 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979950 | GCTGGAAAAAAATTA[A/G]AAGAAGAATGTATTA | 83860 |
rs757249364 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838193 | TCAGTGCTGTGTGTA[C/T]GGGTACCTGCCATGA | 83860 |
rs757251208 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852199 | AAGAGATCCTCTTGC[C/T]TCAGCATTCAAAAGT | 83860 |
rs757255730 | snp | A/T | 1.79897e-05 | 0.00299908 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818704 | CGGTGGCGTCCACGC[A/T]GCGGGATGTGCGAGA | 83860 |
rs757269026 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827519 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 83860 |
rs757279860 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966264 | TCTACAGAACTTTCC[A/G]TAGCATCTTTTATTC | 83860 |
rs757300637 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850706 | ATATGTATATATATA[C/T]ACACACACATACATA | 83860 |
rs757305668 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988168 | TTACTGCTATTAAAT[-/C]AAGGTTATCAGGGCT | 83860 |
rs757307948 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864834 | TATCTTTTTTTTTTT[-/C]CTTTTTATGTTTTGT | 83860 |
rs757335156 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982756 | GGAGAGAGTTTTTCA[A/T]GGCAGTAAATTTAAA | 83860 |
rs757340074 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944531 | GCAACGTTAAAGGAC[-/A]ATAGCAGGTCTAACT | 83860 |
rs757352974 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937791 | GCTCAGCACTCTTAC[A/G]TGCTTTAACTTGTTT | 83860 |
rs757355514 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883859 | TATGGCAGTTGGGAA[A/G]TACAAGGTAGAGGGG | 83860 |
rs757362546 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865010 | ATTTGTTGAATTCCA[A/T]TGCTATGGGAGAAGC | 83860 |
rs757404494 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882916 | TTCTGTGCTGTTTCT[A/T]TGTAGATACATGTTA | 83860 |
rs757419280 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994977 | CCGTCTCAAAAAAAG[-/AA]AAAAAAAAAAAAAAA | 83860 |
rs757439483 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830355 | AAAAATAACCAACCA[C/T]TGTCCTGACTTTGTA | 83860 |
rs757458455 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016480 | AAACAAAGCATCTAT[A/G]TTGAGATATGTGTTT | 83860 |
rs757458726 | snp | C/T | 0.000132622 | 0.00814206 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964206 | GCTTTCTCCAGTCCA[C/T]GTACAGGACAGTACA | 83860 |
rs757460866 | snp | C/T | 1.67091e-05 | 0.00289038 | missense | TAF3 | GRCh38.p7 | 10:7965516 | CCTTGTTCAGCCCTG[C/T]CACAGCCTCCAGGGT | 83860 |
rs757460915 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842566 | AAATTTTTTAGATGC[A/G]GGCTTAAAGCTATAT | 83860 |
rs757466688 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983708 | GCTGGACGTAGTGGC[A/G]TGCACCTATACTCCC | 83860 |
rs757475308 | snp | A/G | 1.66175e-05 | 0.00288244 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964296 | GCCAACTGCAAAACC[A/G]TTAGAAACAAAGTCA | 83860 |
rs757481730 | snp | A/G | 0.000117617 | 0.00766777 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009150 | GCCGAAGACCCCACC[A/G]CCGGCCCCCGCGCCC | 83860 |
rs757511986 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854786 | TATTCAGATCCATAC[A/G]TAGATCAGTAGTATG | 83860 |
rs757512887 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931542 | CAATATTCTACACTT[A/C]TGACATAATGAAACT | 83860 |
rs757519055 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970346 | TGCCAGAATTCAATG[A/G]TTTAATTCTCCCAAC | 83860 |
rs757548045 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938689 | GCAAATGAAACTGAG[A/G]TAAGAGAGGAGGAAT | 83860 |
rs757563859 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859905 | TACGCATCCTTGGTT[C/T]ATGCCTCTCAATCCA | 83860 |
rs757566385 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824930 | TCCTCGCTTATTATT[A/C]AGGCCATGAGTTGAA | 83860 |
rs757577227 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947556 | ACGGCTTCACTGAGG[G/T]GTGACATTAGAGAGC | 83860 |
rs757602642 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869096 | TCTAAAGATTTCACA[G/T]TATATTCTACTTATT | 83860 |
rs757611437 | in-del | -/CTCTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983103 | GCTCTGCCCACCCTC[-/CTCTT]CTCATCTGGCCTCTG | 83860 |
rs757625117 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918865 | TGCAAGGAGGGATAG[C/T]AGGTGGAAGGAAGGA | 83860 |
rs757643005 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932386 | TAGTGTTCCAGCAGA[C/T]AGCACACATGCCGGA | 83860 |
rs757654505 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891221 | AATTTACCCATTTTG[-/A]ATATAAAGGAGTAAT | 83860 |
rs757658361 | snp | C/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819712 | TGTGTTTGTTGAGGA[C/G]AGGAAACTACCACTC | 83860 |
rs757668649 | in-del | -/CAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991464 | CATTGTTTTTTTTCC[-/CAAA]CAAATTGTTAAAATC | 83860 |
rs757676434 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888004 | TGCCCCTGCCACCAC[C/T]GCCATTGTGGTGAAT | 83860 |
rs757680423 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974702 | GACAATGAAGTGAAG[A/G]TTGAAATGTGTGAGA | 83860 |
rs757724493 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876437 | GGTATTTTAAAGTAC[A/G]TATTGTTTTCTAAAA | 83860 |
rs757725841 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888919 | ATGCACACTTCCTCC[A/G]GTGTATATTGTGTCT | 83860 |
rs757728963 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994527 | TTTATTGTTATTTAA[A/C]AAATAGAGATGAGGT | 83860 |
rs757734130 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962807 | AGACATATCTGTTAT[C/T]GCTGCACTAAACTGT | 83860 |
rs757735776 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007950 | AGCTGCTTCCACTGG[C/T]GAGAGTTGTGTGAAG | 83860 |
rs757780971 | snp | A/G/T | 0.000146962 | 0.00857083 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009231 | CGCCCAGGCCGCCGC[A/G/T]GGCCCTGCCCTGCTG | 83860 |
rs757791030 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902095 | ATTTCTTCTCCATAA[-/C]CACCAATTAACATAT | 83860 |
rs757810557 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948979 | CAGAGGGACTGACGC[A/G]CAGAGGTGCTGGGCG | 83860 |
rs757822583 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893464 | AGTTCTGTCTACGTC[A/G]TGACCCATCAGAATC | 83860 |
rs757828339 | in-del | -/TC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900212 | CACTTCCTACCATTT[-/TC]TCTGTTATTTCTTAT | 83860 |
rs757850115 | snp | A/G | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817442 | TAGTCCCTGTCGGAG[A/G]AATATAGAGCCACTC | 83860 |
rs757857849 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859229 | TCATGCCATTGCACT[C/G]CAGCCTGGGCGACAG | 83860 |
rs757867946 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955972 | ATTAAAAGGAATTTG[A/G]CAATTGTTCTGCAGT | 83860 |
rs757870260 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912568 | TGAAAAGCAAGACCT[A/G]ACCCTTCTGGTTATA | 83860 |
rs757887567 | snp | A/G | 3.39305e-05 | 0.00411875 | intron-variant | TAF3 | GRCh38.p7 | 10:7977225 | ATATTGAACTTTAAT[A/G]TGCTAACTTCCACAG | 83860 |
rs757913497 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829337 | TTATTATTAAGTGAC[G/T]CCCGCACTGTATTGA | 83860 |
rs757916591 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883170 | ACAGTTTGTCTGGTT[A/G]TGTTCAGTTAGGAGT | 83860 |
rs757942231 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979362 | AAATGAAAAAAAAAT[-/G]AAAAAAAAAAAAAAG | 83860 |
rs757959195 | snp | A/G | | | upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818371 | CTCCTCCACCTGCGC[A/G]CCCCACGCCCGCTTC | 83860 |
rs757965266 | in-del | -/AGAAGGAGA | 1.65993e-05 | 0.00288086 | cds-indel | TAF3 | GRCh38.p7 | 10:7965654 | AAAAGAAGGAAAAAG[-/AGAAGGAGA]AGAAGGAGAAGGAAA | 83860 |
rs757996641 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988397 | GAGTTCGAGACCAGC[C/T]TGGCCAACATGGTGA | 83860 |
rs758000803 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888948 | CTTGAGAGATTAGCC[C/T]GTGATTGCAGCATAG | 83860 |
rs758008985 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876440 | ATTTTAAAGTACATA[-/T]TGTTTTCTAAAAGTT | 83860 |
rs758026002 | snp | G/T | 5.18551e-05 | 0.00509165 | missense | TAF3 | GRCh38.p7 | 10:7964485 | TCCCAAGAGCCCCAA[G/T]GTCACGACTCACATT | 83860 |
rs758027446 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974776 | GATGGAGTGGAGCAC[A/G]TTTAAAAGTGAGATG | 83860 |
rs758039837 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847673 | TGGTCTCAAACTCCT[A/G]GGTTCAAGTGATCCT | 83860 |
rs758066193 | snp | A/G | 3.20641e-05 | 0.00400388 | intron-variant | TAF3 | GRCh38.p7 | 10:7963872 | TTCTTAGGTTTTGTT[A/G]CATTCCAATAATATT | 83860 |
rs758068300 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962165 | CAGGCTCAAAGCTTT[A/G]AAATTGTGTTTGAGT | 83860 |
rs758092841 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860082 | TCAAGACCAGTGTGG[A/G]CAACATGGCCAAACC | 83860 |
rs758094370 | snp | A/G | 5.57015e-05 | 0.00527709 | missense | TAF3 | GRCh38.p7 | 10:7965708 | GAGAGCGAGAGAAGA[A/G]AGAAAAAGAGAAGGA | 83860 |
rs758100317 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824992 | AATCGTGAGTATTCA[G/T]TGACATTGTGTAGAC | 83860 |
rs758103803 | in-del | -/TGTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944095 | AAATGTTCATGCTTG[-/TGTG]TGTGTGTGTGTGTGT | 83860 |
rs758113568 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997756 | ACAGAAAGCTCTGGA[C/T]GAGAACTTACTATGC | 83860 |
rs758120326 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936581 | AAAGTACTGAGGGTT[A/C]CCATTCACCCACTGC | 83860 |
rs758122095 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943340 | TGATACGTTTGTTTC[C/T]TAGTTCGTAAGTTTT | 83860 |
rs758139189 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006145 | GACCAGCCTGCCCAA[C/G]ATGGAGAAACCCCGT | 83860 |
rs758142881 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830587 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 83860 |
rs758169676 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944814 | TTATCTTAAGCAATT[A/T]ATCAAGAAACTCATA | 83860 |
rs758177406 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932449 | CCAAAGGTCAAGAGA[C/G]AGACTGAGAGAAAGA | 83860 |
rs758184981 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900002 | GGACATGTTAGGCGG[C/T]GTCCACTCATATCCA | 83860 |
rs758213224 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864176 | ATGACAAATACCTGC[C/G]ATTATAACATCATAC | 83860 |
rs758228021 | snp | C/G | 1.66291e-05 | 0.00288345 | intron-variant | TAF3 | GRCh38.p7 | 10:8013694 | GTTTTTTTTCCCATT[C/G]CCTCCATTTTTGCCG | 83860 |
rs758230822 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000792 | TCAAATAATAAATAA[A/G]TAGATAAAACATCTA | 83860 |
rs758231994 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918926 | CAAGGAGGCACTCAC[C/T]TCACCTCCGGACAGC | 83860 |
rs758248192 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981516 | AGAGAACAATATTAT[C/T]ATCAATGGTAATTCT | 83860 |
rs758272617 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826020 | GAATCGGTTCTACTT[C/T]AATAGCATTTTGAAG | 83860 |
rs758294382 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843212 | TCCCAGACTCAAGCA[A/G]TCCTCCCACCTCAGC | 83860 |
rs758296154 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894168 | GTTTGTAATCCAAAG[G/T]TAGAGTCCCTCTCTG | 83860 |
rs758304464 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853287 | TTGGGTGAAAATACT[A/G]TATAACTGTGCCTCT | 83860 |
rs758336048 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984604 | CTTAATGGGTCCAGG[A/T]CTTATTAGTTCCCTT | 83860 |
rs758337147 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982653 | GATCCACCTGCCTTG[A/G]CTTCCCAAAGTGCTG | 83860 |
rs758357904 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939847 | ATTCATGAGGTCCTA[C/T]AGCCAACTAAAAGGA | 83860 |
rs758370379 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001844 | GCACATGCGTAATTA[C/T]TGCATAGTAAAGCAC | 83860 |
rs758373359 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014149 | TAATGTTCTGTAGGA[A/G]CTGTAGCACTGGCCA | 83860 |
rs758388545 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956936 | TCTTCATGTCTTTAA[-/T]TTTTTTTTTGTTGTT | 83860 |
rs758390128 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925632 | AACATGGTGAAACCC[C/T]GTTGCTACTAAAAAT | 83860 |
rs758391683 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968591 | AGTGAGTAATTACTA[C/T]GTGCCAAACACCATG | 83860 |
rs758396518 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840448 | TGAGCCACCGCGCCC[A/G]GCCTGGAAAATGAGT | 83860 |
rs758400767 | snp | G/T | 1.72213e-05 | 0.00293434 | missense | TAF3 | GRCh38.p7 | 10:7964543 | CCCAACAGGACTCCT[G/T]CAGCTACACTCAGTG | 83860 |
rs758447776 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839402 | TATGGTCCTGCTACT[C/G]TATGAGAGTTGAATT | 83860 |
rs758448593 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842787 | ATTGGATAATTATTA[C/T]AATCAAATTAGATAT | 83860 |
rs758456389 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907136 | CCAGGTCTGGCACAT[A/G]TGGAGTAGCAGCAGC | 83860 |
rs758459318 | snp | C/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016604 | GGGGTGGGGGAAGTG[C/G]AAAATAAAGATTATT | 83860 |
rs758468582 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970538 | CAGTCTGCTTTGGTG[A/G]CCTAAGTGACAAATG | 83860 |
rs758475245 | in-del | -/CACACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006199 | ACACACACACACACA[-/CACACACACAC]ACACACACACACACA | 83860 |
rs758499049 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927198 | TTAAAATTAATTTCA[A/G]ATGGTTTTGAGTCAT | 83860 |
rs758533922 | snp | A/G | 3.4951e-05 | 0.00418022 | missense | TAF3 | GRCh38.p7 | 10:7965162 | AAGACAAGAACAAGG[A/G]CAAAAGTAAGGAGAA | 83860 |
rs758541566 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862536 | GAGGCATAATTTATG[G/T]TCAGTAAACTGTACA | 83860 |
rs758553752 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928712 | TCATTCTACTCACGA[C/T]GATCTAGGTAATGGC | 83860 |
rs758606609 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004570 | TTTTCAAAGACATAA[G/T]TTATTTTTCTTTAGC | 83860 |
rs758610127 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985407 | CTCTTCTTTTTTCTC[A/G]TTTTTGTCCAGCCTT | 83860 |
rs758617084 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971407 | GGGAATCTGAACTAG[C/T]GCTTGCTAAATTTGC | 83860 |
rs758631651 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835820 | ACTCGGGTCTCATGG[C/T]GCTTGGTGGCATGTT | 83860 |
rs758652532 | snp | A/G | 1.67276e-05 | 0.00289197 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965361 | GAAAGAGAAGCATAA[A/G]GATAAGAAGAAAGAT | 83860 |
rs758676243 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958997 | CACACAAAATTAGCC[A/G]GGCGTGGTGACGGGC | 83860 |
rs758703650 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849059 | ACAGGAGGCTAAACT[C/G]TAGAATTAAACTTAT | 83860 |
rs758733407 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926306 | GGTGGATTGGCCACT[A/G]CGATGTTGTACATTT | 83860 |
rs758797584 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949583 | TGTCTTCATTTTACA[C/T]AGAAGGAACACAGTA | 83860 |
rs758797673 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979542 | ATCACGGAAATTATA[A/G]CACCCAGGTATTCTA | 83860 |
rs758808051 | snp | C/T | 3.3232e-05 | 0.00407614 | missense | TAF3 | GRCh38.p7 | 10:7964796 | AGAGAATTTCAGGCC[C/T]GGAGTGTACTACTCC | 83860 |
rs758858558 | snp | A/C | 1.80932e-05 | 0.0030077 | missense | TAF3 | GRCh38.p7 | 10:8009136 | CCCTCGCAGAACAGG[A/C]CGAAGACCCCACCGC | 83860 |
rs758860741 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824082 | AATAGCTAATCATGA[A/T]TGTGGTTTTTCTGTG | 83860 |
rs758866977 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951328 | GTTGGCTCAGCCATG[C/T]GGCTCTTCTGCTGGA | 83860 |
rs758875949 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995895 | ACTTGAAGAATCAAC[A/G]TAAAACCGATTCTCA | 83860 |
rs758917960 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825074 | TTTGATTATAAAATG[A/G]TAGCTAATCAGGTAT | 83860 |
rs758919314 | in-del | -/AG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981003 | ATGGATTTTAGGGAC[-/AG]GGGCTGTTTGGATGG | 83860 |
rs758924181 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950329 | GAGCAGAATATGTGG[G/T]CATGAAGACCCTGTG | 83860 |
rs758926895 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997617 | TTTTATGAATAACGC[C/T]AGTGTTTATAGCAGT | 83860 |
rs758932573 | in-del | -/ATAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873815 | AACTTAATGCTGTTT[-/ATAG]ATAGAAAACTGTTGC | 83860 |
rs758941109 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905189 | TTTATGAAATACACC[C/G]TACGTTAGAGTTTGA | 83860 |
rs758976513 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945816 | TCTCTCCACACACAT[A/T]ATCCCATTTTACTGT | 83860 |
rs758980242 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938939 | AATGATAGGAAGATA[A/C]TAAAAAATGTATAAA | 83860 |
rs759006738 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909100 | CCGTGGAGGCCTGCC[A/G]GGGGCCATTGCTGGA | 83860 |
rs759013002 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895042 | ACCATTCCTGGCTAA[-/T]TTTTTGTATTTTTAG | 83860 |
rs759025999 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866594 | CTGAGGGAGCGTGGC[A/G]TAAGATGAAGCAGAG | 83860 |
rs759030330 | snp | A/G | 0.000314619 | 0.0125384 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8013793 | CAAGCCTGACGATGG[A/G]AGTCCCATGATTGGG | 83860 |
rs759041540 | snp | A/G | 3.36033e-05 | 0.00409884 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965043 | CAAGGTGTATGAGGA[A/G]AAAACCAAGCTGCCT | 83860 |
rs759055843 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914686 | ATGTCTAGTTTCTTC[A/G]TATACCTTTTTCTGA | 83860 |
rs759099235 | snp | C/T | 2.79341e-05 | 0.00373715 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009291 | CAGTGCCAAAGCCCC[C/T]GTGCGCAGCGTGGTG | 83860 |
rs759112262 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886595 | TTATCAGTTAGATGA[A/G]GGTAATAATATCTCA | 83860 |
rs759117412 | in-del | -/TTTTGTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996855 | CTATTTTTTTTTTTT[-/TTTTGTA]TTTTTGTATTTTTGT | 83860 |
rs759145486 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840944 | AACCTCCACCTCCCA[G/T]GTTCAAGCTATTCTC | 83860 |
rs759167287 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887487 | TCTCTTTTTCTCTGT[G/T]TCTTTTCTTTTTCTT | 83860 |
rs759201264 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003586 | AATGTCTGTTGATAT[A/G]ATTTCAGATTACACA | 83860 |
rs759221375 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821155 | AATTACCAAGTTTCC[A/G]TAGCCAGTTTCTTGG | 83860 |
rs759232788 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908815 | TTATGAAGAGCTGCC[C/T]GTCTCCCAGAGCAGT | 83860 |
rs759233480 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992539 | AAAGAGGTTTGGGGA[A/G]AGTAGAATTTGAGTA | 83860 |
rs759240858 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910629 | CAAATGATCCACCCA[-/C]CTCGGCCTCCCAAAG | 83860 |
rs759252768 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979766 | TAAATCTAATAGTAA[C/T]AGAATTTTATGTAAA | 83860 |
rs759261957 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012151 | CACTGCACTCCAGCC[-/T]TGGGTGACAGAGTGA | 83860 |
rs759265695 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983464 | TACTTTAGATGTAAC[A/G/T]TTTGGGAACATTTCA | 83860 |
rs759266086 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833577 | TTTGGGGACCCAGCA[A/G]TACTGCTGATTTATT | 83860 |
rs759269679 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866949 | TAAATTCCAAACTGA[G/T]GAAAGCAGTTTTTAA | 83860 |
rs759279349 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946925 | TCTTTTTTTAAAAAA[A/G]TAATTATTTGTTTGT | 83860 |
rs759280592 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993352 | CCCAGCTAATTTTTT[G/T]ATTTTTTGTAGAGAT | 83860 |
rs759305942 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824634 | TTAGCTTTCCATGCT[A/G]TGTCAACTTTATAAA | 83860 |
rs759316113 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998895 | ATTAAAGGGCACTGG[A/G]AAAGAGTCAGGTAAG | 83860 |
rs759322394 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867978 | ATTATTAAGAAAATC[A/G]TAAGGAAGAGAAAAT | 83860 |
rs759372776 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847958 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGG | 83860 |
rs759389164 | in-del | -/T | 1.68752e-05 | 0.00290471 | frameshift-variant | TAF3 | GRCh38.p7 | 10:7964445 | AGAAAAGAAATCACC[-/T]TGGACGTTCCAAGAG | 83860 |
rs759453688 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989617 | ATTAAAACTTTTGAT[A/G]GAAATTACAAAATTT | 83860 |
rs759454562 | snp | C/G | 1.66952e-05 | 0.00288917 | missense | TAF3 | GRCh38.p7 | 10:7977274 | GCTCTGGCCCCGAGT[C/G]CAGTTATCCCCAGAT | 83860 |
rs759461108 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896700 | CAAAATACTTGATTA[A/G]TAAGTGTGGTAGTTT | 83860 |
rs759465258 | snp | C/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8017045 | ACTGTTCAGTGGCCT[C/G]TGTGAAATGAACTGG | 83860 |
rs759477969 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000618 | CACACAAAAAAATAC[A/G]TATACAAAAAATTAG | 83860 |
rs759480926 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959164 | CACACACACACACAC[-/AA]AAAAAGTTTCAGGCT | 83860 |
rs759490214 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838211 | GTACCTGCCATGAGT[C/T]GGATCCTACACAAGG | 83860 |
rs759496708 | in-del | -/AAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856859 | TAACAGCTGGTTCTC[-/AAA]AAAAAAAAAAAAAAA | 83860 |
rs759497900 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843332 | TAGACTGGTCTTGAA[C/T]TCCTGGGCTCAAGCG | 83860 |
rs759516829 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892315 | GAAAGCATGCTCAGT[A/G]TGGGTGAGCTGCTGA | 83860 |
rs759524422 | in-del | -/CAAGAGTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014007 | ATTAACTGCAAAACC[-/CAAGAGTG]CAAGAGTGCTTAGAC | 83860 |
rs759550293 | snp | A/C | 1.72624e-05 | 0.00293784 | intron-variant | TAF3 | GRCh38.p7 | 10:7977208 | ACTTTTGTTGAAAAA[A/C]CATATTGAACTTTAA | 83860 |
rs759566725 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846259 | ACTGCGCCCGGCCAA[A/G]AGGATGAAGTTTTTA | 83860 |
rs759572648 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942279 | GAGTATATAAATATT[A/G]CTTATCTGAAAAGAT | 83860 |
rs759575548 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928266 | TGTTTAACTCACTGC[C/T]GTGTCCCAGTACCTG | 83860 |
rs759576436 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913039 | TGAGACCTCTTTCCT[C/T]GGCTTGCAGGTGGGC | 83860 |
rs759602301 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870370 | GGATATGTTCTCTCC[A/G]TTTTTACTTATAGTT | 83860 |
rs759619093 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901799 | GACTAAGGCTGTGAC[A/G]GTCACATTTAAATAA | 83860 |
rs759627111 | snp | A/G | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818065 | GAAGGGCTTTGAAGG[A/G]CATGCGGAACAGCTT | 83860 |
rs759640989 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912281 | TATTAAAAAAAAGAA[A/C]TGGAGACAGGGTCCC | 83860 |
rs759682395 | in-del | -/TGTTCAAAGT | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817409 | AAAATGTGAATATCA[-/TGTTCAAAGT]TGTTCAAAGTTCTGG | 83860 |
rs759684513 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008474 | ACAGTTTTATTGACA[A/G]TGGCATTGAGAGTAT | 83860 |
rs759701081 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888580 | GTTTGCTTTCAGTCT[A/G]CAGTGATGTGTAACA | 83860 |
rs759744947 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931835 | TGACTGACAGTTCCT[A/G]CCTGCTCAAAGTATT | 83860 |
rs759758312 | in-del | -/CACACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006197 | ACACACACACACACA[-/CACACACACAC]ACACACACACACACA | 83860 |
rs759803699 | snp | C/T | 1.66646e-05 | 0.00288652 | missense | TAF3 | GRCh38.p7 | 10:7964603 | AAACAAATACAGACA[C/T]CCCCTGATGCTGGGA | 83860 |
rs759829971 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936945 | ATCACACAGTATGTG[A/G]CCTTCTCAGTTTGAC | 83860 |
rs759832910 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974223 | GCAAGGGTCTTGCTC[C/T]ACCCGCCACCCATCC | 83860 |
rs759851377 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858746 | AGCACATGTTAGCAG[C/T]TATGAATTATTTTAA | 83860 |
rs759867720 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859700 | GGGCATTATGGCTGC[A/G]CTTTATTTTACTCAT | 83860 |
rs759880398 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922703 | AGTTTATTACTAAGT[G/T]ATTGGTGTTTCATAA | 83860 |
rs759884114 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975384 | CTTATCTTAAGACTT[A/C]CTAGGGTCAGATCCT | 83860 |
rs759885013 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905776 | TAATCCCAGCTACTC[A/G]GGAGACTGAGGCAGG | 83860 |
rs759885158 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892417 | ACTTTTCTTTGTTCT[A/G]CTTGATTACAAAATT | 83860 |
rs759889579 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966033 | AGCTTAAAAAAAACA[A/C]ATCTGGGTTCTTAAA | 83860 |
rs759937080 | snp | C/T | 1.65993e-05 | 0.00288086 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964260 | GCCGCCAATGTTGGC[C/T]CCAGTTGCAAAATCA | 83860 |
rs759955944 | snp | A/G | 1.67775e-05 | 0.00289629 | missense | TAF3 | GRCh38.p7 | 10:7965323 | CCCAAAGTGAAATTG[A/G]AAGATGGACTTGTGA | 83860 |
rs759958201 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867255 | AGAGTGAGACTGTCA[-/CA]CACACACACACACAC | 83860 |
rs759958476 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966648 | GCCCTCTAAAAGTTA[C/T]CTTCTTTGAGCTTGG | 83860 |
rs759984776 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852696 | GAATGTGTGGGTGTG[A/T]TTTTAGCAAACATTG | 83860 |
rs759985447 | in-del | -/AAG | 6.96702e-05 | 0.00590172 | cds-indel | TAF3 | GRCh38.p7 | 10:8014704 | CCCAAGTGTGCGAAC[-/AAG]AAGAAGGACAAAAAG | 83860 |
rs759987974 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880054 | TCTCTACAAAAAATA[G/T]AACAAATTAGCTGGC | 83860 |
rs759997675 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941650 | GCCTTCGAGGCTGTG[-/A]AATCCTTTCCTTCTG | 83860 |
rs760001601 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827210 | TGAGACATGACTCAG[C/T]GAGTCACTGAGTTTC | 83860 |
rs760009796 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839739 | TATTCTTCTATTCAG[G/T]TTACTTTTTCTGCTT | 83860 |
rs760011789 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013283 | CACATTTGGCTGTCT[A/G]TATTAATTCCATGCC | 83860 |
rs760012338 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856206 | AGAAAAGATTTTGGC[G/T]GGGCGCAGTGGCTCA | 83860 |
rs760025188 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822122 | TATGATTAAAGTGGT[A/G]TTTTAAGAAAATTGT | 83860 |
rs760061031 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839034 | GTGGTGTTCAGTACA[C/G]GTGTCTTAGCATAAA | 83860 |
rs760100308 | snp | C/T | 1.66682e-05 | 0.00288684 | missense | TAF3 | GRCh38.p7 | 10:7965483 | CACTGGTGTTGCCCC[C/T]AAAAGAGTTGGCCCT | 83860 |
rs760124522 | snp | C/T | 1.66001e-05 | 0.00288094 | missense | TAF3 | GRCh38.p7 | 10:7964853 | TCACAAAGTCAGGAT[C/T]CACTCCTCTGCCTCT | 83860 |
rs760126567 | snp | A/C | 3.9178e-05 | 0.00442578 | missense | TAF3 | GRCh38.p7 | 10:8009275 | CCGCCGCCTCCGGGG[A/C]CAGTGCCAAAGCCCC | 83860 |
rs760131441 | snp | A/G | 1.65776e-05 | 0.00287898 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964164 | AGAGCCACTCAGCTC[A/G]ATAAATACTCAAAAG | 83860 |
rs760131857 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906073 | GTGCTCGTGGATAAC[A/C]CTTGATGCTATGAAA | 83860 |
rs760162826 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993459 | GCTGAGATTATAGGC[A/G]TGAGCCACCATGCCC | 83860 |
rs760175135 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887156 | AGAATTGCTTGAACC[C/T]GGGAGGTGGAGCTTG | 83860 |
rs760186134 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943368 | TTTTCCTGGGTAAAC[A/G]TTTGGAGGGTGTTTT | 83860 |
rs760186525 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925114 | ACTAATACTGGCAAC[A/T]TAACGAGTTTTCTGT | 83860 |
rs760198705 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005702 | CTTGTGTGTTCAACC[A/G/T]GTATGGGAAACTGCC | 83860 |
rs760212722 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904875 | CTGTGCTCCCTTTAG[A/G]CTGCACACATGAACC | 83860 |
rs760227008 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940053 | CCAGAGATTAGGAGG[-/A]AATTATATGTGCTTG | 83860 |
rs760258793 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822171 | AAGAGATTGAAGTGG[G/T]CAGAACTTGAGACTA | 83860 |
rs760266955 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863436 | GCCAGGATGGTGAAA[C/T]CCCGTCTCTACTGAA | 83860 |
rs760277003 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852049 | TCAGCATCTCAAAGC[A/G]CTGGGATTATAAGTC | 83860 |
rs760304151 | snp | G/T | 1.80273e-05 | 0.00300222 | missense | TAF3 | GRCh38.p7 | 10:8009129 | GCCGGCGCCCTCGCA[G/T]AACAGGCCGAAGACC | 83860 |
rs760320649 | in-del | -/GA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979362 | AAATGAAAAAAAAAT[-/GA]AAAAAAAAAAAAAGG | 83860 |
rs760324154 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856946 | AAAACATTTACAAAT[A/G/T]CTAATGAGATAAGCA | 83860 |
rs760371212 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896880 | GTCGAGCCCAGATGT[C/T]AGCCCAGTTGGAAGG | 83860 |
rs760376610 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981069 | CAACTCTTCTATAAA[A/G]CTCAAATTCAGGTAA | 83860 |
rs760378133 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013636 | ATATGCCTGTTTATT[C/T]GGTTAACAGTATAAA | 83860 |
rs760403989 | in-del | -/CAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959163 | ACACACACACACACA[-/CAAA]AAAAGTTTCAGGCTT | 83860 |
rs760430014 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982291 | GATCTTCTTCCCTAA[G/T]ATCAAGGGAAGAAAA | 83860 |
rs760432443 | snp | C/G | 1.83717e-05 | 0.00303076 | missense | TAF3 | GRCh38.p7 | 10:7965668 | GAGAAGGAGAAGAAG[C/G]AGAAGGAAAGAGAGA | 83860 |
rs760438117 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864638 | GAGTAGAATGGTGGG[A/G]TTATACGGCTTGTTT | 83860 |
rs760440468 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835024 | GTGTGTGTTTCTCTC[A/G]TACTTTCATTGTCTG | 83860 |
rs760445463 | in-del | -/AGA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988751 | GAGATTCTGTCTCTC[-/AGA]AAAAAAAAAAAAAAA | 83860 |
rs760465928 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986147 | TATTTTTTTTCCCCC[G/T]TCTTTTCTTTTTGCC | 83860 |
rs760482296 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906690 | GTAATGAAGGAACCA[A/G]ACGAATTAAATAGAG | 83860 |
rs760492310 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990494 | TTGAATGACCGCTAC[A/T]TCTTTTTTCTCGCCT | 83860 |
rs760502889 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884744 | CTAGGACTGGTCATT[G/T]CTATTACAATGTCAT | 83860 |
rs760540743 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831783 | CCTTCTGGTATATCA[A/G]AATGTTCTAGACTCA | 83860 |
rs760546372 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988579 | ACCCTGTCTCAAAAA[-/AAAAAAAAAAAAAAAA]AAAAAAAAGAAGCCA | 83860 |
rs760550023 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015707 | GTGCCCGGAAACATG[A/G]TGGGGAAAGGGCCCG | 83860 |
rs760554261 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897769 | GGCTCAAGCGAGCCT[C/T]CTGCCTCAGTTTCCC | 83860 |
rs760556480 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929732 | ACATTATTTAATCAA[C/T]ATTACCAATAAATAA | 83860 |
rs760575909 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833247 | TTGCTGGATTATATG[A/G]TAATTCTATTTTGAG | 83860 |
rs760605827 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826595 | TTATAAACATTTTAA[A/G]AGGAAAATAACAAAT | 83860 |
rs760611412 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887552 | GGAGATGAGAGAGCA[A/G]AGTAGATGAAAATGC | 83860 |
rs760614354 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978588 | CTTTTGAAACCAGCT[A/G]TCTGGTATACCTAAT | 83860 |
rs760626843 | snp | A/G | 1.6676e-05 | 0.00288751 | missense | TAF3 | GRCh38.p7 | 10:7964596 | CCAGGTAAAACAAAT[A/G]CAGACACCCCCTGAT | 83860 |
rs760636060 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005420 | AAGTCCAAATTACTT[C/T]AAAGTATCCTAGAAC | 83860 |
rs760659070 | in-del | -/G | 1.92617e-05 | 0.0031033 | intron-variant | TAF3 | GRCh38.p7 | 10:8009351 | ACCTGCCGCCCGCGC[-/G]GGTTAGCATGGAGAC | 83860 |
rs760672478 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850956 | CTGATTGTGTGTGCC[A/G]GTCACTATCATGAAC | 83860 |
rs760695488 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992850 | ATTTAACAGTTATCA[A/G]AATGTTGCCATACTT | 83860 |
rs760704567 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932134 | GAGCATATTCAATAC[A/T]GGGAGTATAGTCACT | 83860 |
rs760729886 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848277 | CTCTAGTGTACAGTC[C/T]TAATTATGTCTGACA | 83860 |
rs760742897 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930849 | ATTTTTTATACTTTT[C/G]TATATAAAAATATAA | 83860 |
rs760753954 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933419 | GAGCCAAAGGCTGCA[C/T]GACGAGCTCTGATGC | 83860 |
rs760757140 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930422 | CGTACAGCCCTATTT[C/T]TAGAGTAGGGAGTAC | 83860 |
rs760759769 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919608 | CATAGAGAATCCTCA[A/G]ATGCTCAAGTCCCTT | 83860 |
rs760805295 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951068 | AACAAGGGTATGCAT[C/T]GATTAGCTGATGAAA | 83860 |
rs760838182 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997353 | ATTACTGGTTTCATC[A/G]TGTTTGCACACAATA | 83860 |
rs760842383 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963668 | CTGTTGGGAGGTCGG[A/G]GGCTGGGGGAGGGAT | 83860 |
rs760849628 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889726 | TCCTGTCCTATATCC[C/G]TATCTTGTGAAATAG | 83860 |
rs760882466 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866154 | AGTTCCTCCAGTATG[C/T]ATATGTTCCTTTTAT | 83860 |
rs760902631 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877113 | GGATTTTTAAAATAC[G/T]TTTTACTTTATAACT | 83860 |
rs760915538 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895001 | CTGCCTCAGCCTCCT[C/G]AGAAGCTGGGATTAC | 83860 |
rs760984522 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840351 | TAGAGATGGGGTTTC[A/G]CCGTGTTAGCCAGGA | 83860 |
rs761002719 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835502 | TTCATGTCAGTTTTC[C/G]TTTTTCTGGCCAGCT | 83860 |
rs761021741 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894721 | AATATTTAACAGAAC[G/T]AATGGAACTATTTTA | 83860 |
rs761029383 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950080 | TATTATTAGCCTGTA[A/G]TGGTGGTTTAGCAGC | 83860 |
rs761047299 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830010 | CAAGTGAATTCGTTA[C/T]GAAATGGAAGTGTCT | 83860 |
rs761059934 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968152 | AAGTGAGACATATCT[A/G]CTCACTTTATGTGAG | 83860 |
rs761068220 | snp | A/G | 1.68224e-05 | 0.00290016 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965292 | GTTTAAAATCAAAGA[A/G]TTTGAAGATGTTGAT | 83860 |
rs761071492 | snp | A/G | 1.89288e-05 | 0.00307637 | intron-variant | TAF3 | GRCh38.p7 | 10:8009380 | ACGTTTTCAGATCGA[A/G]ACAAGTGTGTGCTCT | 83860 |
rs761076776 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882753 | TTGTAGAATGTAGTA[C/T]GTAACCACTGGGGTA | 83860 |
rs761098468 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933890 | ACGTTTTCCCCCCGA[-/T]TTTAGCATTTCTGAA | 83860 |
rs761102190 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841592 | CTGAGAAGGATGGAC[C/T]CAAGAGGAGATGTCA | 83860 |
rs761134850 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943192 | CAGCGCTGCCTTTGC[C/T]GTTGCCTTGAATGAA | 83860 |
rs761138002 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002665 | GAATATTCCGCACTG[A/G]TTGAAGACAGATTTT | 83860 |
rs761165828 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865665 | CAAAGTAGCAACTAG[A/G]TTCATTCTTAGAGTT | 83860 |
rs761169197 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839864 | CCAGCAAGATTTAGC[A/G]CCTCAGCGGAGGTGT | 83860 |
rs761171867 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982491 | GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 83860 |
rs761176409 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838496 | GAGCGATTCTCCTGC[C/T]TTAGCCTTCCAAGTA | 83860 |
rs761177489 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878810 | TGGGGCTCACTGCAA[A/C]CTTTGCCTCTGGATT | 83860 |
rs761185204 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828549 | CTCTCCCCAGCTTGC[C/T]ATACATATTTTCAGA | 83860 |
rs761230788 | in-del | -/TGTGTGCACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000965 | GACATATCATTTGTG[-/TGTGTGCACACA]TGTGTATCACCACTT | 83860 |
rs761246818 | snp | A/G | 1.65616e-05 | 0.00287759 | missense | TAF3 | GRCh38.p7 | 10:8013788 | TGTAACAAGCCTGAC[A/G]ATGGGAGTCCCATGA | 83860 |
rs761275259 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937246 | GTATGTTTAGTTTTG[C/T]AAGAAACTGCCAAAC | 83860 |
rs761276886 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825900 | TATAGTAATTGTCTA[C/T]TTAATTTTTGAGGAA | 83860 |
rs761328319 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938197 | TAAAGATTCATGGAG[C/T]TTAAAAATCCCTAAC | 83860 |
rs761362994 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920911 | CCAAATCTTAAAGCT[A/T]ACTGACCTTCCATTT | 83860 |
rs761364845 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828625 | AGGAATGTCTGAAAA[C/T]AGTACAGCGTACTAT | 83860 |
rs761365163 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946322 | TGGCTGTCCACATGC[A/T]GTCCCTGCACCTGGA | 83860 |
rs761388631 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845155 | TAGCATTTCAAAGTG[C/T]ATTGTTTTTTTACTA | 83860 |
rs761432840 | snp | C/T | 0.000359686 | 0.0134057 | missense | TAF3 | GRCh38.p7 | 10:8009121 | GAGGCCAAGCCGGCG[C/T]CCTCGCAGAACAGGC | 83860 |
rs761454294 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870660 | GTTTTTAGGCCTTAA[C/G]GAGCGGCAGAACTCG | 83860 |
rs761474150 | snp | A/C | 1.65605e-05 | 0.0028775 | missense | TAF3 | GRCh38.p7 | 10:7824387 | GGGTTAGTCTACATG[A/C]ACTAGAAGACTATAT | 83860 |
rs761478576 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015548 | TTTATGAAGTAGTTA[A/T]TTTTTAAATTTTTAT | 83860 |
rs761484545 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931050 | TTGCCATCTGATGCC[A/T]GTAAAAGCATCTAAT | 83860 |
rs761524512 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926458 | ATTACCAGGTCCATA[C/T]AGTATAAACAGAATT | 83860 |
rs761525965 | snp | C/T | 1.65776e-05 | 0.00287898 | missense | TAF3 | GRCh38.p7 | 10:7964145 | TTGTGTTATTGGAAG[C/T]TCGAGAGCCACTCAG | 83860 |
rs761527155 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884671 | GGGATTACAGGCGTG[C/T]GCCGCTGCGCCTGGC | 83860 |
rs761533146 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002920 | CAAATTGGAACCTTT[C/T]ATCATCAGGAAGTAG | 83860 |
rs761533941 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841709 | TTTGGAGATAGATAA[A/C]TTGTAGAGGATGTGC | 83860 |
rs761541361 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901397 | CAAAGAAATTAATTA[C/T]CCAGTATGAAAACAA | 83860 |
rs761542392 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968465 | GCTTTGGAATCCAGC[A/G]GACCTGGAATAAGAT | 83860 |
rs761546180 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986980 | CTCACCCTTCCCCCA[A/G]GTTAATCACTGCTGA | 83860 |
rs761582545 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864896 | CCTAAGATCACAAAG[A/G]TTTTTGTCCTGTGTT | 83860 |
rs761585412 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854347 | CTACGTAAGATAACT[A/G]GAAGGAATTATTTGC | 83860 |
rs761587507 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839929 | CCCAGCATACACAGA[C/T]TGAGAGGGACTTTAC | 83860 |
rs761589922 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899674 | AGAGGAAAAGCTTAG[A/G]TGTTCACAGTAAACA | 83860 |
rs761607731 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969528 | GATGAGTATACAGGA[G/T]TACTTTAATTACAAT | 83860 |
rs761612713 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967616 | ATAATAAATAGTAAT[A/G]TCTATAGAATTAGAC | 83860 |
rs761654262 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970849 | GTTTGTACCTTTAAG[A/G]AAGGGTTTTCATCCT | 83860 |
rs761663503 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006842 | CATGGCACGGGGCCG[A/G]CAGTTCCCATCTGGA | 83860 |
rs761720552 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008351 | TAATCCACCCACCTC[A/G]GCCTCCCAGAGTGCT | 83860 |
rs761720853 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988602 | AAAAAAAAAAAAAAA[A/G]AAGCCAGATATAATG | 83860 |
rs761732712 | snp | C/T | 4.36015e-05 | 0.00466892 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009183 | CCCCGGCCCCATGCT[C/T]GTCAGCCCTGCGCCC | 83860 |
rs761773382 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919400 | GGGTGTACTGTCCTG[C/G]TGTTACTTAGGGTCA | 83860 |
rs761774089 | in-del | -/GG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978421 | CAACTTGGTTTTCCA[-/GG]GGGGAGTGTATACCC | 83860 |
rs761792561 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993982 | TAGGGTTTTGGAAAG[A/G]GGAAGGGTTCTGTCT | 83860 |
rs761803159 | snp | A/T | 1.66299e-05 | 0.00288352 | missense | TAF3 | GRCh38.p7 | 10:7964766 | AATCTGAAGGAGACA[A/T]TTTTACTAGCCCTAA | 83860 |
rs761805004 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961445 | ATCCTCGTTGACCTC[G/T]TAAGCATTTGGCTTT | 83860 |
rs761829189 | in-del | -/ACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959154 | CACACACACACACAC[-/ACA]CACACACAAAAAAAG | 83860 |
rs761829251 | snp | C/T | 1.91529e-05 | 0.00309452 | intron-variant | TAF3 | GRCh38.p7 | 10:7965781 | CCTATCTGAACAGAG[C/T]CCTAGTGAGAAACAC | 83860 |
rs761829307 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846695 | AATATCCACTGGACC[G/T]CCTATAAAGCTAAGA | 83860 |
rs761851300 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874995 | CTTCTTAATCCTTCA[A/G]AATGTGCTGTTTTTC | 83860 |
rs761853707 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920678 | AAAGTCAGAATTGAG[A/G]TGAAAATCACAGTTA | 83860 |
rs761854937 | snp | C/T | 8.6166e-05 | 0.0065632 | missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818848 | CTGCAGCAGCTGGGC[C/T]GGGGCTGCCATCGGT | 83860 |
rs761866685 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836553 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 83860 |
rs761873209 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887603 | ATAAGTGTGAACTGT[A/T]TAGGCAAGATGAATT | 83860 |
rs761897634 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955269 | AAAGAGGAATCTATT[-/A]TAAAAACAGTGACAT | 83860 |
rs761903691 | in-del | -/A | 1.65583e-05 | 0.00287731 | frameshift-variant | TAF3 | GRCh38.p7 | 10:7965178 | AAAAGTAAGGAGAAG[-/A]GATAAAGTGAAAGAG | 83860 |
rs761908533 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922722 | GGTGTTTCATAACTA[A/G]CTGCCAGTTTTACAT | 83860 |
rs761919982 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993213 | GGATGAGTTCTTACT[C/G]TGTCGCCCAGGCTGG | 83860 |
rs761925365 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934407 | CCTTATATAAAAATC[C/T]TAATGTCCTTCCATT | 83860 |
rs761934490 | snp | A/G | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965424 | AGAGAAAGAAAAAGT[A/G]AAAGATAAAGGCAGA | 83860 |
rs761943313 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853411 | TACAGATCATGGCAT[A/G]ATTTATTGTCTTTTT | 83860 |
rs761975159 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985226 | GCTGATTAGACTTGC[C/G]TTTTGGGTTCCAAAC | 83860 |
rs761979648 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891021 | AGTACACATGGAAGC[A/G]TTGAATTGGGGCCCC | 83860 |
rs761989646 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952353 | GTGATTAACGATAGC[A/T]ATTTATTGTATCTGA | 83860 |
rs762013113 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856124 | AAATCATGGCAGCAG[A/T]AATTTTTTTAAAATG | 83860 |
rs762029769 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896647 | ATACTTTTTCCTTCA[G/T]TATTGAGCTTTTAGG | 83860 |
rs762030794 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878507 | TCTTGATCTGAGTGT[A/G]TTCAGCTTGTGGAAA | 83860 |
rs762044540 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840465 | CCTGGAAAATGAGTG[-/T]TTTGATATTTACTAT | 83860 |
rs762044572 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915637 | GACAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAA | 83860 |
rs762051448 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011125 | ACCAACTCTGCAGAC[C/T]GTGATGTGTTAGCCT | 83860 |
rs762063896 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994827 | AAAAAAAAAAAAAAA[-/T]AGCTGGGTGTGGTGG | 83860 |
rs762071045 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895475 | TCTTGAAACCAATGC[A/T]TCACACTTTCTTACT | 83860 |
rs762090445 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951219 | ATATGAATACATAGC[C/T]AACATGCTGTTGTGT | 83860 |
rs762096381 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825941 | GTTTTCCACAGTGGC[A/T]GTACCATCTAAGCTT | 83860 |
rs762111577 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871726 | TGGAATTACAGGCGG[C/G]AGCCACCGCGCCAGG | 83860 |
rs762142894 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004074 | TATTTTTTTTGAGAC[C/T]GATTCTTGCTCTGTC | 83860 |
rs762147953 | in-del | -/GTGAG | 0.000162509 | 0.00901267 | intron-variant | TAF3 | GRCh38.p7 | 10:7975095 | AAAAAAAAAAAAAGA[-/GTGAG]ATGAAAATAATTCGT | 83860 |
rs762165194 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903787 | CATGTTTAAGAAATA[C/T]GTATTATTTTGCTTG | 83860 |
rs762171711 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939679 | AGAGGAACCAGCTGT[C/T]AAAGAGCCAGAGCAA | 83860 |
rs762187873 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819668 | TAATAGAAGCTCCAC[A/G]TTATCTTGTTGATGT | 83860 |
rs762192470 | snp | C/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016426 | GGGTGTCATTGCCCT[C/T]GTTGTTCAAGAGGCC | 83860 |
rs762206160 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848663 | GCCTCAAATGAAGTT[A/G]TTAGTGTTTTCATTT | 83860 |
rs762211377 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913371 | GTCACACAGCAGCCA[C/T]TCCAGCTCTCATTCG | 83860 |
rs762227873 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989551 | ACGATATTGCGTAGT[C/T]AAATGTAATATTGTT | 83860 |
rs762235013 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842137 | TTGTCATTGTAGGAT[A/G]TTGAATTAATATTGT | 83860 |
rs762252536 | in-del | -/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839691 | TTTCTTGAGTACAAT[-/TA]TTTTTTTTTTAATTG | 83860 |
rs762275243 | snp | C/G | 1.73785e-05 | 0.0029477 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964503 | CACGACTCACATTCC[C/G]CAAACACCTGTGAGA | 83860 |
rs762279385 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975646 | TGCCGAGCATCTCCT[G/T]CATGCAGGCATCATG | 83860 |
rs762287092 | snp | C/G | 1.67069e-05 | 0.00289019 | missense | TAF3 | GRCh38.p7 | 10:7964969 | CCTTCAAATATGCCC[C/G]CCAACTTTCCTTATA | 83860 |
rs762291477 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862221 | CTTGGGCTCCTCTTA[C/G]TGATGGTCTCATTTG | 83860 |
rs762297671 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978832 | TTAATCTTGACTCCC[A/T]CACAGAAGTTTGGCT | 83860 |
rs762301994 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855460 | ATGTCCAGCCTCCTT[C/G]CATTTGAGATGCTGG | 83860 |
rs762302170 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969906 | CTGCTTCCTTCCTCC[A/G]TCTCCTTCCTCCCAT | 83860 |
rs762303378 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830352 | TCCAAAAATAACCAA[C/T]CACTGTCCTGACTTT | 83860 |
rs762319077 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938406 | CTCGCCTAAGGTAGC[C/T]AATGGGAATAATAAA | 83860 |
rs762319202 | snp | A/G | 1.89672e-05 | 0.00307949 | intron-variant | TAF3 | GRCh38.p7 | 10:8009378 | AGACGTTTTCAGATC[A/G]AGACAAGTGTGTGCT | 83860 |
rs762343612 | in-del | -/TTTTCTTTCTTTCTTTTTTTTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948245 | TTTTTTTTTCTTTTC[-/TTTTCTTTCTTTCTTTTTTTTTT]TTTTCTTTCTTTCTT | 83860 |
rs762351787 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889862 | CTCCTAAATATTAAA[G/T]TCATATTATTTTCTA | 83860 |
rs762395141 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917641 | CTCTGGAGAATAGGT[C/T]GGGTTCTGAGGCCGT | 83860 |
rs762397356 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818296 | TTGCCTCTAAAACAC[C/T]GGCGTTTTCGTCACC | 83860 |
rs762414645 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884964 | AATTGCTAACCCATA[C/G]CAATATATCTGGAGT | 83860 |
rs762420449 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926728 | TTCTTTTTTTCTTCC[A/T]TTTTAGAATCTGAAT | 83860 |
rs762441328 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003184 | TATTTTGTGCTACTT[A/C]TTTAGTGTTCAGTGG | 83860 |
rs762442317 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945698 | CTGAAATGCTTGTTC[A/G]TGACATCATCACACA | 83860 |
rs762471103 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913427 | TGCAGCCTTTTTCTA[G/T]GCCCTTTTCTCATAA | 83860 |
rs762473375 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928013 | TTGATGAAGAATTAT[A/T]TGTTTTACGGCCTCT | 83860 |
rs762476975 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831207 | GAAAGCAGGGTTAAC[A/G]CTTGATTTTTTTCAT | 83860 |
rs762482440 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842047 | GCCAGGCACCACGCC[C/T]GATGTGGGAGGCAGA | 83860 |
rs762507913 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901996 | GCTCCTCCAGACTTT[A/G]TGTTCGGAACCACTG | 83860 |
rs762508616 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956952 | TTTTTTTTTGTTGTT[A/C]GTGTCTTTTTTCTAC | 83860 |
rs762510424 | snp | C/T | 1.68267e-05 | 0.00290053 | missense | TAF3 | GRCh38.p7 | 10:7965054 | AGGAGAAAACCAAGC[C/T]GCCTTCCTCCGTGGA | 83860 |
rs762518932 | snp | C/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828922 | GTAGTCCCAGCTACT[C/G/T]GGGAGGCTGAGATGG | 83860 |
rs762533049 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843170 | TCACCCAGGCTGGGG[C/T]GCATATAGCTTACTG | 83860 |
rs762584938 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861294 | TGTATTTTTAGTAGA[G/T]ATGGGGTTTCACTAT | 83860 |
rs762591463 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859363 | CACATCCTGCCTTCA[G/T]ATCCTGCCATGTGGA | 83860 |
rs762604091 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864749 | TTCCTCTCAGCCTGT[A/G]GTTTGCTTTTTCATT | 83860 |
rs762608199 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948387 | AACCAGTGCGCCCAG[C/G]CTTCGTCTGATTTTA | 83860 |
rs762620142 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886477 | AAATATATAATAACC[A/G]AAGAAAAGTTTGGTT | 83860 |
rs762622982 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016844 | CCCTTGCTATTTCAT[A/G]GTTGCTTTCCTAAAT | 83860 |
rs762641030 | in-del | -/CTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999301 | CTCTTAGGAAATTGA[-/CTGT]CTAATGTGGATGAGA | 83860 |
rs762651448 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889527 | CTGGATTCACAACCA[C/T]TCTGACTCCAGGAAC | 83860 |
rs762652571 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970854 | TACCTTTAAGGAAGG[A/G]TTTTCATCCTTTTCC | 83860 |
rs762660711 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873016 | ATAAGTAGTTTAAAA[A/G]CAAACAGAAATCTTA | 83860 |
rs762700938 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847832 | GAGTGCACTGGTGCA[A/G]TCTGGGCCCACCGCA | 83860 |
rs762716346 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958409 | AGCTACCATTGGACA[C/T]TTCTGCAGCAGTGAA | 83860 |
rs762723177 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004975 | AAATTTATTTTGTCC[C/T]AATACTCAGTTTATA | 83860 |
rs762735843 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876086 | TATAATTTATCTTGT[C/T]TGTATAATAAAGGGA | 83860 |
rs762747594 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944913 | CCAGAATTTTGTCAA[G/T]GTCATTTAGAGCACT | 83860 |
rs762753232 | in-del | -/ACACACACACAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959154 | CACACACACACACAC[-/ACACACACACAA]AAAAAGTTTCAGGCT | 83860 |
rs762775663 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009949 | GGGGATTTCACTCTG[C/T]CACCGAGGCTGGAGT | 83860 |
rs762788626 | snp | A/G | 3.32635e-05 | 0.00407807 | missense | TAF3 | GRCh38.p7 | 10:7964732 | GAGCCAGATCCTTTC[A/G]AATTTTCTTCTGGAT | 83860 |
rs762807113 | snp | C/G | 1.79783e-05 | 0.00299814 | missense | TAF3 | GRCh38.p7 | 10:8009115 | GCCCCCGAGGCCAAG[C/G]CGGCGCCCTCGCAGA | 83860 |
rs762814413 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867702 | GCTTTGAATAGGAAG[C/G]AAGATTAATGTCTTT | 83860 |
rs762814947 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949894 | CAGGCAGTGACTGCG[C/T]ATCACCACTGCCTGT | 83860 |
rs762843324 | in-del | -/GACAGATTATATT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971515 | AAATAAAAAACCTTG[-/GACAGATTATATT]GACAAAGCTGCCCAT | 83860 |
rs762859974 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950813 | CCATCTCAGTAGTGC[C/T]ATGTTTTTCTCATTC | 83860 |
rs762863488 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866929 | TTTTAGATCAATGTG[A/C]AATTTAAATTCCAAA | 83860 |
rs762870928 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907259 | ACAGCCCTTCTGCAG[A/G]GCTGTCATTGGTGCG | 83860 |
rs762881862 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816603 | GTCCAGTCTTCTTGT[C/T]TGGATTCAGGGAAGC | 83860 |
rs762898121 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983308 | AGAAGGAAAGGAGGG[C/T]TCACACCAGAATAAG | 83860 |
rs762900626 | in-del | -/AT | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007257 | GATAAATCAGGAGAC[-/AT]AAAACTAAGTGGGAA | 83860 |
rs762909044 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855743 | GAGCAAAACCAACTA[A/T]AAAGCAACTTAGAGG | 83860 |
rs762919729 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908457 | CTATTTCATGTGAGC[A/G]GCTGTGAAGATTAAA | 83860 |
rs762923979 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895278 | TGAGTGCCTTCTGTT[G/T]CAGTGATTTCAACTT | 83860 |
rs762935850 | in-del | -/CAAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898545 | AACAAGACTCTGTCT[-/CAAAAAAAAA]AAAAAAAAAAAAAAA | 83860 |
rs762973502 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952409 | TCGTTATCATAAATC[A/T]TATCATAAATAACCA | 83860 |
rs762974013 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892123 | ACAACTTTATGCATT[A/G]CAAAATTCAGATGCA | 83860 |
rs762986518 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865889 | CTTGCATCTTGTCAG[C/T]GTTGATTTATGCAGA | 83860 |
rs762992934 | snp | A/C | 1.6641e-05 | 0.00288448 | missense | TAF3 | GRCh38.p7 | 10:7964618 | CCCCCTGATGCTGGG[A/C]AACTGAACAGTGAGA | 83860 |
rs762999382 | snp | A/C | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015903 | ACTGTAGCATTTTGT[A/C]TTTATATTGTTTTAT | 83860 |
rs763011999 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825978 | AGCAGTGCCCAAGGG[C/T]TCCAATTTCTTGCAA | 83860 |
rs763068105 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923921 | AACTGTTGAATTTCG[A/T]TTTGGAAATAAAGGA | 83860 |
rs763068424 | in-del | -/ATC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843858 | TGTTAGTTAAATTTT[-/ATC]ATCCATTTTACTCTT | 83860 |
rs763068968 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858311 | TACAAGCAATTGCCA[C/G]TAATATTGTATCATT | 83860 |
rs763069867 | snp | C/T | 1.66849e-05 | 0.00288828 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965497 | CCAAAAGAGTTGGCC[C/T]TGCCCTTGTTCAGCC | 83860 |
rs763072965 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867885 | CAATAATGTAAACGG[G/T]CGATTAACACGTATT | 83860 |
rs763077808 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836544 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 83860 |
rs763104885 | snp | C/T | 9.9369e-05 | 0.00704802 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8013820 | TGGGTGTGACGACTG[C/T]GATGACTGGTACCAC | 83860 |
rs763108000 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972834 | GTTAATGTCAGTTTC[C/T]ATATAAACTAGTTAG | 83860 |
rs763122794 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911188 | TGATATGATCAAAAC[C/T]CACTTCTTTAGAAAA | 83860 |
rs763123926 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879937 | AACCTGGCTGGGCAC[A/G]ATGGGTCACAACAGT | 83860 |
rs763177103 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880957 | AGGATTCTCTTAGCC[C/G]AAGCATGGTGGCTCA | 83860 |
rs763208355 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872987 | ATAATTTATCCATAA[A/G]TCCCAAAGTCTCTAT | 83860 |
rs763237204 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986372 | ACCCAGCATTATTTC[C/T]GCCAGTGTGGTTCTT | 83860 |
rs763239144 | snp | C/T | 3.27327e-05 | 0.0040454 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818829 | GGACGTGCTGCAGCG[C/T]TATCTGCAGCAGCTG | 83860 |
rs763259597 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998416 | GAACATATGCACAAG[A/C]AGACATTTCTGAGAT | 83860 |
rs763261067 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005313 | ATTATGTGCTGCTTA[-/T]TTTTTTTTAAAGATA | 83860 |
rs763272644 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857130 | AATGAGGAAGACAAA[A/G]GTGAAACAACACATA | 83860 |
rs763293975 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952618 | GGTTGGCTTGCTTAT[-/A]TAGCATTTTAGTTTT | 83860 |
rs763321154 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011381 | ACCTCAGCCTCCCGA[A/G]TAGCTGGGACCACAG | 83860 |
rs763325553 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824343 | AGACCCAATTTTGGA[C/T]GATGTTGGTGAAGCT | 83860 |
rs763361596 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903906 | AAGTATTCAGAGATA[C/T]ATAACGTGAGATAAC | 83860 |
rs763364158 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979298 | TCTGTGAGCTGAGAT[C/G]GCGCCACTGAACTCC | 83860 |
rs763412784 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891125 | TAATCTAGTAAGTCA[A/G]TTGAACAGAGGCTGC | 83860 |
rs763427870 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851573 | ACAACAATTAACTTC[C/T]GTCATCACCCAGCTT | 83860 |
rs763437192 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819884 | AAGTTTCGTTCCCGC[C/T]TCCACAGGGCTGCCA | 83860 |
rs763439583 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922966 | AAACCGCTTAATAAC[A/G]TTAGTTTCTCTTAAT | 83860 |
rs763450423 | snp | A/G | 1.72934e-05 | 0.00294048 | missense | TAF3 | GRCh38.p7 | 10:7965615 | AGGAGAAAGAAAAGA[A/G]AAAGGACAAAAAGGA | 83860 |
rs763473329 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832715 | CCACCACACCCGGCT[A/G]ATTTTTGTGTTTTTA | 83860 |
rs763482905 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849919 | ATCCTGAGCTCGGGC[A/G]GTCTACTCACCTTGG | 83860 |
rs763508728 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983138 | CGGTGGCAGAGGTGG[C/T]CCTGGCCACTCAGGC | 83860 |
rs763548375 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892591 | GGTAAAATAGAATAT[A/T]TTGTCAAATTATAAA | 83860 |
rs763555155 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820931 | GGTCCTTGAGTATAC[C/T]GTTAGTGATAGGCTA | 83860 |
rs763585864 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960574 | CACGGGGAATCGCAT[A/G]TGCAGAGGTACAGGA | 83860 |
rs763587080 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844666 | CAGGCATGAACCACC[A/G]TGCCTGGCCAGCTTT | 83860 |
rs763588042 | in-del | -/GGG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849658 | ATTATAACAACTATT[-/GGG]GGGGTTCATGCGAAC | 83860 |
rs763612687 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822175 | GATTGAAGTGGGCAG[A/G]ACTTGAGACTATACT | 83860 |
rs763622165 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935603 | AAATAAATAAATAAA[G/T]CAAGCAAGCTAAAGC | 83860 |
rs763628929 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937195 | GTTCATTTGGGTAAA[C/T]GCCAGGGAGTGTGAT | 83860 |
rs763655511 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954526 | AGTGCACTCCATAGG[C/T]GAATGAGTGAATTAG | 83860 |
rs763658104 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993791 | CTAGTCATTCCTTTC[A/T]CATGTATTAGCTGAA | 83860 |
rs763669055 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864644 | AATGGTGGGGTTATA[C/T]GGCTTGTTTGTCTTT | 83860 |
rs763671009 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852072 | TATAAGTCTGAGCCA[C/T]CATGCCAAGCCTTTC | 83860 |
rs763690432 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012705 | AGGAAGTTTTCCTGT[C/G]AATGTAGTTTGCCTT | 83860 |
rs763703038 | in-del | -/ACACAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863722 | CATATATATATACAC[-/ACACAT]ATATATATATACACA | 83860 |
rs763722832 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920810 | GGAAATTTGGTAGCA[C/T]TGAAATAGAATTTTT | 83860 |
rs763723359 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935993 | GATTGTAGGGGCTCA[C/T]GGAGGGAAGCAGCAA | 83860 |
rs763737346 | snp | A/T | 4.99122e-05 | 0.00499536 | missense | TAF3 | GRCh38.p7 | 10:7964033 | ATTAATGATGAGAAT[A/T]TCCTGGGCAAGAGAC | 83860 |
rs763775573 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922435 | TTTTCTGTAAAACAT[-/A]AGATGATTATCAAGT | 83860 |
rs763787501 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966884 | AAAAGTGAAATGGGA[A/T]TTCTGATATCAATAA | 83860 |
rs763787964 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986211 | TGTTCTCATTTTCTC[G/T]TTAGGTTTGTTATGC | 83860 |
rs763808264 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887571 | AGATGAAAATGCAAC[A/G]TAAGACTTTCCTAGT | 83860 |
rs763815472 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005510 | GGGAATCCTTAGTGT[C/T]GGGAGGGAGTTCTAT | 83860 |
rs763837780 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972649 | TATACCATTTTAAAT[C/T]TCACTTATGTGTTTC | 83860 |
rs763838168 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845121 | TGATTACACCAGTGT[C/T]CCAGCAGTCTCCCTG | 83860 |
rs763839513 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968351 | TTAAATTTTTCAATC[C/T]CCACATTTATTTTAC | 83860 |
rs763865476 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839263 | AATATATATCTCTAC[C/T]ATCATACTTCATATA | 83860 |
rs763868410 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992891 | GTCTTTTTATTCCCA[A/G]CGCATTTCCAAACAA | 83860 |
rs763879216 | in-del | -/ATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963205 | TACCTGTCATTCCTG[-/ATA]ATAATAATAATAATC | 83860 |
rs763888317 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008142 | CACTCTGTAGCCCAA[G/T]CTAGAGTGCAGTGGC | 83860 |
rs763900604 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852984 | GATCTCATGGATTTA[A/T]ACAGATTTGATAGAT | 83860 |
rs763923876 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958943 | ATCGAGACCATCCTG[A/G]CTAACATGGTAAAAC | 83860 |
rs763933668 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821386 | AACAAACACTTACTG[A/T]GCATCACTTACGAAC | 83860 |
rs763939099 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971378 | GAGTTTTTTTCTAAC[A/G]TACCGGCATAGATGG | 83860 |
rs763960091 | snp | A/G | 4.99081e-05 | 0.00499515 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964749 | ATTTTCTTCTGGATC[A/G]GAATCTGAAGGAGAC | 83860 |
rs763961824 | snp | A/G | 1.8635e-05 | 0.0030524 | utr-variant-5-prime, missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818684 | AGCAGTGGCAGCAAG[A/G]GCTGCGGTGGCGTCC | 83860 |
rs763980987 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904907 | CAATTCCCCGCACTT[C/T]CTCCACCACCCGCTC | 83860 |
rs763982689 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833976 | TGCCTGCTGTCCTCC[A/G]GCACAGGACAACAGC | 83860 |
rs764003104 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874842 | ATGTATCATGTAACT[A/G]TTCAAAACACATAAA | 83860 |
rs764036790 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006450 | CCCACAATTGGCTTT[C/T]AAGTGCTTAGGACAG | 83860 |
rs764047794 | snp | C/G | 3.49107e-05 | 0.00417782 | missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818833 | GTGCTGCAGCGCTAT[C/G]TGCAGCAGCTGGGCC | 83860 |
rs764057737 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862808 | TGGTCTGGCCTTTTT[C/T]CACCAATATAATTAT | 83860 |
rs764067413 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833257 | ATATGGTAATTCTAT[C/T]TTGAGTTTTTGGAGG | 83860 |
rs764069156 | snp | G/T | 3.32795e-05 | 0.00407905 | missense | TAF3 | GRCh38.p7 | 10:7965445 | TAAAGGCAGAGAAGA[G/T]AAGATGAAAGCCCCA | 83860 |
rs764084441 | snp | A/G | 1.6631e-05 | 0.00288362 | missense | TAF3 | GRCh38.p7 | 10:7964631 | GGAAACTGAACAGTG[A/G]GAATCAGCCGAAAAA | 83860 |
rs764087105 | in-del | -/GCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949018 | CAAGAGCTGTGCCCG[-/GCT]GCTGCTGCCGCCGCT | 83860 |
rs764091718 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933499 | GAAGGTGACTGTTTC[A/C]GTTGTGATAACATCT | 83860 |
rs764093490 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877220 | ATGAGTCTTTAGAAA[A/T]AATTTATACTGATTT | 83860 |
rs764119067 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916971 | TGTGCTCGAAAGAAC[A/G]TAGGCTTTGGATTCA | 83860 |
rs764127265 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888279 | CTTAACCTTCCTAAG[-/C]TTTCCTCACTCTAAC | 83860 |
rs764145348 | in-del | -/GTGTGTGTGTGTGTGTGTGTAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920312 | TACGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGTGTAT]GTGTGTGTGTGTGTG | 83860 |
rs764164625 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832669 | ATTCTTGTGCCCCAC[C/T]CTCCCCAGTAGTTGG | 83860 |
rs764210225 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907923 | ACAACCAGCAGGAGT[A/C]GATGGGGACTGAATC | 83860 |
rs764231872 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835687 | CCAGCCTCAGCCGCT[C/T]TTCTCGGGTTGGCCT | 83860 |
rs764235303 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866236 | CCGTCACTCTTCCAG[A/G]CACGGGGGATGGAGC | 83860 |
rs764240545 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978593 | GAAACCAGCTATCTG[A/G]TATACCTAATGCCCC | 83860 |
rs764253634 | snp | A/T | 7.96929e-05 | 0.0063119 | intron-variant | TAF3 | GRCh38.p7 | 10:8014600 | AGAATAGATGTCTGT[A/T]TAAAAGTTGCTTATC | 83860 |
rs764289142 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010014 | CCTCCCAGGCTCAAG[C/G]GATCCTCCCACCTCT | 83860 |
rs764295714 | snp | C/T | 3.32265e-05 | 0.0040758 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964287 | ATCACAAATGCCAAC[C/T]GCAAAACCATTAGAA | 83860 |
rs764304710 | in-del | -/CC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873619 | ACATCCGAGTTCTCC[-/CC]CCCCCCCCCCGTCAA | 83860 |
rs764309845 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997369 | TGTTTGCACACAATA[A/G]CTGAATAATGAGGAT | 83860 |
rs764345247 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858915 | CTCCATTACTGCTGG[C/T]CTCTTCAGCGTCTTC | 83860 |
rs764363480 | snp | C/T | 4.01663e-05 | 0.00448124 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009228 | GCTCGCCCAGGCCGC[C/T]GCGGGCCCTGCCCTG | 83860 |
rs764373571 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839876 | AGCGCCTCAGCGGAG[C/G]TGTATACATGTCAGC | 83860 |
rs764409064 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882833 | AAAGATACAAGAATA[A/G]CACAAAGAATTCCTA | 83860 |
rs764416376 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012583 | GGATGTTCCACCAGC[C/T]TTGGCCTCTAGACAG | 83860 |
rs764421521 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870499 | TTCTGGTGGTTCATT[A/G]TAAAATACATTTTTT | 83860 |
rs764421594 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951069 | ACAAGGGTATGCATC[A/G]ATTAGCTGATGAAAA | 83860 |
rs764436442 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951113 | GACTTATAGGAACCT[A/G]ACCGTGTATTTCTCT | 83860 |
rs764442537 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999426 | TGTCTAAAGGCTGTT[-/A]AAAAAAAAAAAAGAA | 83860 |
rs764442685 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878460 | GGAGGGAGGGGTGAC[A/G]GGAGGAGTAAGGGTA | 83860 |
rs764443035 | snp | A/G | 3.33985e-05 | 0.00408633 | missense | TAF3 | GRCh38.p7 | 10:7964409 | TCGGAAGTCCTATTC[A/G]ATCACCAAAAACTGT | 83860 |
rs764444492 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821358 | CACCCCTTTAAATCC[C/T]TTCTGTTGTTTTAAC | 83860 |
rs764459697 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976038 | TTTGGAAATGCAGAG[C/G]TTTTGTTTAGCTTGT | 83860 |
rs764470909 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925914 | GCTGGGATTGTAATA[A/C]TCTCTTAAGACTGGT | 83860 |
rs764474441 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869467 | TGTTAACTTATCCTC[A/G]TGGGAGCATAGTGTT | 83860 |
rs764488867 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988306 | ATTAAAAAGATATCC[A/G]GGGCTGGGCACAGTG | 83860 |
rs764532737 | snp | A/G | 2.15329e-05 | 0.00328116 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009312 | CAGCGTGGTGACTGA[A/G]ACGGTCAGCACCTAC | 83860 |
rs764552464 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838530 | GAAATTACAGGTGTG[C/T]ACCACCACGCCTGGC | 83860 |
rs764573617 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955622 | AATGTCTATGAACTT[C/T]TTAGATTATAGTGTT | 83860 |
rs764586119 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901573 | CAGTTCCATTTGGCC[A/C]TCAGCTTTTTTCCCA | 83860 |
rs764622685 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880849 | TTAAACGATATACCT[A/G]CTAATATTACCATAT | 83860 |
rs764647603 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967169 | GTCAGTTACACTGCA[A/G]AGAGACTTCACGTGG | 83860 |
rs764664658 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938251 | AGTTTGGTGTGGCTA[C/G]GGATGGGGAGGTGTG | 83860 |
rs764701538 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830059 | CCCTTCCCAAGAATA[A/G]CCTAGTTGGCAGATG | 83860 |
rs764729964 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859845 | CTTAGTAAATGTTGG[A/T]CAAATGGCCGTTTCC | 83860 |
rs764742490 | in-del | -/AAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999427 | TGTCTAAAGGCTGTT[-/AAAA]AAAAAAAAGAAAGAA | 83860 |
rs764744676 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902203 | CTGAGGCAGGCGAAT[A/C]ACTTGAGGTCGGGAG | 83860 |
rs764748826 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859042 | CTGAGGCGGGCAGAT[C/T]ACGAGGTCAGGAGAT | 83860 |
rs764760643 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895199 | TTCCTTGGTAACTTG[A/G]TAACAGCTTTAGTGA | 83860 |
rs764792783 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982574 | CGGCTAATTTTTTGT[A/G]GTTTTAGTAGAGATG | 83860 |
rs764795551 | snp | A/G | 1.66871e-05 | 0.00288847 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964005 | AGATGATGAATTGGA[A/G]GAGGAAGAAATTATT | 83860 |
rs764798950 | snp | A/G | 1.73003e-05 | 0.00294106 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014779 | GGCTGGACCAAGCGG[A/G]GTCAGCCCGGGCTTC | 83860 |
rs764805882 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854359 | ACTGGAAGGAATTAT[G/T]TGCCCCAAAACAATT | 83860 |
rs764813130 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882900 | TTACATCGTTTGCTT[G/T]TTCTGTGCTGTTTCT | 83860 |
rs764835056 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913400 | CGCCCAGGCTTGATC[C/T]AGGCAATACTTTGCA | 83860 |
rs764835715 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001781 | TTTGAGGGATTTTTT[A/T]AATTAACTATACCAT | 83860 |
rs764844798 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866795 | CCTGCAGTGTTGGAC[A/G]CATCAGGTTAAATAA | 83860 |
rs764860568 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926555 | TTTTATATGTGAACA[A/G]TTGTTGCTGCTTCTT | 83860 |
rs764861778 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884709 | CTTTTTTTGAAGAAT[A/C]GAGTCTAGAATCCAG | 83860 |
rs764890106 | in-del | -/TACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974133 | ATTCCTTCTGAAACA[-/TACA]CACACACACACACAC | 83860 |
rs764907293 | snp | G/T | 1.67044e-05 | 0.00288997 | missense | TAF3 | GRCh38.p7 | 10:7964965 | AACACCTTCAAATAT[G/T]CCCCCCAACTTTCCT | 83860 |
rs764925563 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912407 | GCCTGGCCAAAAATG[A/G]TAGTTTTTATGGGTA | 83860 |
rs764941001 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955866 | ATGAAGGAAAATTGA[A/C]ATGGAGTTTGTGGTG | 83860 |
rs764986537 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007020 | GCTGGCAATTCCTGG[A/T]GAGGTGAGGATGGCC | 83860 |
rs764991810 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910835 | CACAAACCAGACTAG[-/A]TTTTTTAAAAAATAG | 83860 |
rs764992076 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943289 | ACGCATCACGTTCTG[C/T]TTGCTCCTTAGCATT | 83860 |
rs764997611 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829215 | TTTACAGAAAAAATT[A/G]AGAAGTTAGTTTGGA | 83860 |
rs765001159 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961480 | ACCTGCCTTCTGCAT[A/G]AAACTCTTGCTCCCT | 83860 |
rs765013609 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864704 | TATCCTGGTCATCAG[G/T]TTTTTATCATCTATT | 83860 |
rs765031135 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958511 | AAAAAAAATTATAGT[A/G]TCATACTATTTATGT | 83860 |
rs765039340 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841827 | TCTGGAGTGAGAATT[C/T]AGAATGGACCTTATA | 83860 |
rs765051970 | in-del | -/TA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848808 | ATGCCAATATGCCTT[-/TA]TATATATCTATATGC | 83860 |
rs765063709 | in-del | -/CCAAGAGCCCCAAGAGTC | 1.69591e-05 | 0.00291191 | cds-indel | TAF3 | GRCh38.p7 | 10:7964454 | AATCACCTGGACGTT[-/CCAAGAGCCCCAAGAGTC]CCAAGAGCCCCAAGG | 83860 |
rs765063813 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918606 | TTGCTGATATAGAAG[C/T]GGATGCACCAGGGGG | 83860 |
rs765094437 | snp | A/G | 1.66935e-05 | 0.00288903 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7977288 | TCCAGTTATCCCCAG[A/G]TTAACTCTCCGAGTC | 83860 |
rs765096330 | snp | A/C | 1.73261e-05 | 0.00294325 | missense | TAF3 | GRCh38.p7 | 10:7964532 | GACCTGAAACGCCCA[A/C]CAGGACTCCTTCAGC | 83860 |
rs765103013 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835365 | AGATTCAGGGTAGCT[C/T]CTCTGACTTTGCAGT | 83860 |
rs765129693 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921440 | ATACCTCCCCTCCCC[C/T]GTTTAAACTTTCTGA | 83860 |
rs765132201 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894099 | CTTTTCGCCTTTTAT[A/G]TTGTCTTGCAGTAAG | 83860 |
rs765158121 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823260 | TTTAAGATTCTGCAG[A/G]TGCATCAGGGAACAA | 83860 |
rs765191339 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837807 | CTGGGTGACAGAGTG[G/T]GACCCTGTCTCAAAA | 83860 |
rs765211851 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867061 | GTCAGGAGTCTGAGA[C/T]GAGCCTGGTGAACAT | 83860 |
rs765224974 | snp | A/G | 1.71422e-05 | 0.0029276 | intron-variant | TAF3 | GRCh38.p7 | 10:7977215 | TTGAAAAACCATATT[A/G]AACTTTAATGTGCTA | 83860 |
rs765235288 | in-del | -/TATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998242 | AATCTGAGTGAGAAC[-/TATA]TATATATATATATAT | 83860 |
rs765246816 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928463 | AATGCATTTATGGAA[A/T]TCTTCAAATTGTGTC | 83860 |
rs765268764 | snp | A/G | 1.65625e-05 | 0.00287766 | missense | TAF3 | GRCh38.p7 | 10:8013815 | ATGATTGGGTGTGAC[A/G]ACTGCGATGACTGGT | 83860 |
rs765291484 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951225 | ATACATAGCTAACAT[C/G]CTGTTGTGTAACAAG | 83860 |
rs765297078 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853475 | TGTAGATTAAACTTC[-/A]AAAATGTATAGTATC | 83860 |
rs765323322 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889005 | GGATGGTTGAGGCAC[-/T]TTTTTTTTTCTACAC | 83860 |
rs765338336 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872794 | TATCAAACTACTAAA[A/G]TAGTATTAAAGCACA | 83860 |
rs765374162 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878544 | AGGCCACACACTTAG[A/G]GTATATTAACTTTGT | 83860 |
rs765376533 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011226 | TATTTGTTGTTATAA[A/G]CTGTACAATATTACA | 83860 |
rs765378534 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997476 | AGGACGGGCTCTTTA[C/T]TGACTTGACAAGCTG | 83860 |
rs765395048 | snp | C/T | 1.6664e-05 | 0.00288647 | intron-variant | TAF3 | GRCh38.p7 | 10:8013687 | TCTTTTTGTTTTTTT[C/T]CCCATTCCCTCCATT | 83860 |
rs765436867 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985258 | TTCTTACATCCCCCA[C/T]GGCTTGTCGTCCAGG | 83860 |
rs765451090 | snp | C/T | | | missense | TAF3 | GRCh38.p7 | 10:7965728 | AAAGAGAAGGAGAAA[C/T]ACAAGCATGAAAAAG | 83860 |
rs765467113 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902430 | CTCTGTCTTAAAAAA[A/T]AATAATAAAAAAAGA | 83860 |
rs765488868 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847653 | TCTTGCTGTGTTGCC[C/G]TGGTTGGTCTCAAAC | 83860 |
rs765499253 | snp | A/G | 3.32082e-05 | 0.00407468 | missense | TAF3 | GRCh38.p7 | 10:7964270 | TTGGCTCCAGTTGCA[A/G]AATCACAAATGCCAA | 83860 |
rs765521892 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939687 | CAGCTGTCAAAGAGC[C/T]AGAGCAAGTTAGAAA | 83860 |
rs765523300 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830576 | GCAAACTCCACCTCC[A/T]GGGTTCAAGCGATTC | 83860 |
rs765576945 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928663 | ATAAGGATGAATGTT[A/G]TAATGGTTTTTCTAT | 83860 |
rs765624121 | snp | A/G | 3.33317e-05 | 0.00408224 | missense | TAF3 | GRCh38.p7 | 10:7965485 | CTGGTGTTGCCCCCA[A/G]AAGAGTTGGCCCTGC | 83860 |
rs765629173 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917721 | CTAACAAGCAGTTGT[A/G]CTACTGGACTAGATA | 83860 |
rs765636984 | in-del | -/AAG | 2.71054e-05 | 0.0036813 | cds-indel | TAF3 | GRCh38.p7 | 10:8014725 | AAGGACAAAAAGCAC[-/AAG]AAGAGGAAGCATCGA | 83860 |
rs765638169 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903790 | GTTTAAGAAATATGT[A/T]TTATTTTGCTTGGAA | 83860 |
rs765641182 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975715 | GGGATTTGAAAAACA[A/G]CTCTAGGAAGAGACA | 83860 |
rs765705565 | snp | A/G | 3.31549e-05 | 0.0040714 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964176 | CTCAATAAATACTCA[A/G]AAGATCCCACCAATG | 83860 |
rs765713498 | in-del | -/CCGTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869245 | CCTTCCTGACTTCTA[-/CCGTGT]GTGTGTGTGTCTGTG | 83860 |
rs765723726 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962889 | ACTTTATCATTGTAC[A/T]TTATATGCTTAGTTA | 83860 |
rs765737029 | snp | A/G | 1.65941e-05 | 0.00288041 | missense | TAF3 | GRCh38.p7 | 10:7964084 | GAAGAACTGCCAGCC[A/G]TGAAGCGGCCTCGGC | 83860 |
rs765756391 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933866 | CATGTTTTATGGATT[C/G]AAAGATGCACGTTTT | 83860 |
rs765761997 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944866 | TTAATTCTAAAATAG[A/C]TTTAGAGCCCCAGGT | 83860 |
rs765772326 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013053 | TAAATAAAGTCAACT[C/G]TAGAGTACACAATAT | 83860 |
rs765780073 | in-del | -/TGTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944093 | TAAAATGTTCATGCT[-/TGTG]TGTGTGTGTGTGTGT | 83860 |
rs765813692 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840850 | TGTTTTCTTTTCTTT[C/G]TTTCTTTTTTTTTTT | 83860 |
rs765815986 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819694 | GATGTGAAGCATTGT[A/G]TGTGTGTTTGTTGAG | 83860 |
rs765838066 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848827 | ATATCTATATGCCAC[A/G]TTTCATAACTCTTCT | 83860 |
rs765867561 | snp | A/G | 1.65608e-05 | 0.00287752 | missense | TAF3 | GRCh38.p7 | 10:7824410 | GACTATATTCACAAC[A/G]TTGAGCCTGTCACCT | 83860 |
rs765881947 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991153 | TTTGGAAACTTTCTT[A/T]TGTACATAGATACAT | 83860 |
rs765886577 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819849 | AGACTCACAGACACA[C/T]GCTGTATTTCTTAGG | 83860 |
rs765900811 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877821 | TTTTTTTAACCACAT[A/G]CTCAATTCTGTGTCC | 83860 |
rs765904497 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010274 | AAAAGTTACATCACA[A/G]TGTTCACATAGTCAG | 83860 |
rs765937125 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989881 | GTATATGTATGTCAA[C/T]TCTGGCTGTGATATC | 83860 |
rs765949812 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884976 | ATACCAATATATCTG[C/G]AGTTTAATTTTTGTT | 83860 |
rs765964658 | in-del | -/AAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827791 | CTCAAAAAAAAAAAA[-/AAC]AAAAACAAAAACAAA | 83860 |
rs765976557 | snp | C/T | 0.000206249 | 0.0101529 | missense | TAF3 | GRCh38.p7 | 10:8009197 | TCGTCAGCCCTGCGC[C/T]CGTGCCGCTGCCGCT | 83860 |
rs765986005 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861362 | CCACCCACCTTGTCC[C/T]CCCAAAGTGCTGGGA | 83860 |
rs766001908 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962475 | GTAGAATAAAGATTA[A/T]GTTTCTTTTTCTGGA | 83860 |
rs766049641 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902531 | AAACTCAGGGGAAAA[A/G]CGTTTCTCAGGGTTT | 83860 |
rs766079074 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881304 | TTCCCACCATGTGTC[A/G]CAATACTTTACTGTA | 83860 |
rs766098261 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947281 | GCCCCTCCAGCCCCC[-/A]ACCGCAGGCCGGATA | 83860 |
rs766130877 | in-del | -/CACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006199 | ACACACACACACACA[-/CACACAC]ACACACACACACACA | 83860 |
rs766144098 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823788 | TACAGGCCTGCGCCA[C/T]CACGCCCGGCTAATT | 83860 |
rs766145354 | snp | A/C/G | 5.2282e-05 | 0.0051126 | intron-variant | TAF3 | GRCh38.p7 | 10:7977190 | GGAGAAGTGGTAGGA[A/C/G]GTACTTTTGTTGAAA | 83860 |
rs766146509 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008486 | ACAATGGCATTGAGA[C/G]TATTAAGAAGAAACA | 83860 |
rs766155079 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933877 | GATTCAAAGATGCAC[A/G]TTTTCCCCCCGATTT | 83860 |
rs766162348 | snp | A/G | 3.66596e-05 | 0.00428117 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965670 | GAAGGAGAAGAAGGA[A/G]AAGGAAAGAGAGAAA | 83860 |
rs766163037 | in-del | -/ACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863718 | TACACATATATATAT[-/ACAC]ACACATATATATATA | 83860 |
rs766168696 | in-del | -/TTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842518 | AGAAGAACTAAAATC[-/TTT]AGTTTTGTTCTAAAA | 83860 |
rs766174834 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853463 | TGGTGGTGAAAAATG[C/T]AGATTAAACTTCAAA | 83860 |
rs766189691 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898674 | GCACTGGGTTCTTAT[-/A]AAAACCGCTGTGCAA | 83860 |
rs766194906 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936691 | GGCACATCATAGTCA[A/G]CAGAGACCACAGTTT | 83860 |
rs766203867 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835461 | TTTGTTTTCCTCCAC[C/G]ACTTTTACCTGGATC | 83860 |
rs766226249 | in-del | -/TTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838354 | CCTTTACCAAGCCAG[-/TTT]TTTTGTTTTTTTTTG | 83860 |
rs766243065 | snp | A/G | 1.65965e-05 | 0.00288062 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824556 | CATTGTGTCTTCTCA[A/G]GAAGGTTTGTGAGTG | 83860 |
rs766254651 | snp | A/G | 1.70229e-05 | 0.00291739 | missense | TAF3 | GRCh38.p7 | 10:7964459 | CCTGGACGTTCCAAG[A/G]GCCCCAAGAGTCCCA | 83860 |
rs766264107 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824612 | TTTTAATGGATTTTT[A/G]ATCCTCTTAGCTTTC | 83860 |
rs766280034 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902199 | GAGGCTGAGGCAGGC[A/G]AATCACTTGAGGTCG | 83860 |
rs766320987 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911234 | GCAAACATGAGGAAG[A/G]GACTGAGTATTCAAA | 83860 |
rs766362080 | snp | A/G | 1.97295e-05 | 0.00314076 | intron-variant | TAF3 | GRCh38.p7 | 10:8009337 | ACCTACGTGGTGCGT[A/G]CCTGCCGCCCGCGCG | 83860 |
rs766390163 | in-del | -/C | 9.94497e-05 | 0.00705088 | intron-variant | TAF3 | GRCh38.p7 | 10:8013865 | GCGCCCTGCCGGCCA[-/C]CACTCATTAGGCAGC | 83860 |
rs766396347 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896942 | TTGTTCCTTGCATCC[A/G]TAGGACTGAGGTACC | 83860 |
rs766417738 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895471 | CTTTTCTTGAAACCA[A/G]TGCATCACACTTTCT | 83860 |
rs766439969 | snp | A/G | 1.73694e-05 | 0.00294693 | missense | TAF3 | GRCh38.p7 | 10:7964525 | CCTGTGAGACCTGAA[A/G]CGCCCAACAGGACTC | 83860 |
rs766464458 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854043 | ACACACACAATCATT[C/T]GCCCCACTCAGCCAG | 83860 |
rs766465732 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934601 | AAGCACCCGCCACCA[C/T]GCCTGGCTAATTTTT | 83860 |
rs766477948 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883425 | GATGAGTCCTGTGAT[A/G]CTGATTTGATGGTAA | 83860 |
rs766487786 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826036 | AATAGCATTTTGAAG[C/T]GTTACCTATTTGTCT | 83860 |
rs766489757 | snp | A/C | 3.78422e-05 | 0.00434968 | intron-variant | TAF3 | GRCh38.p7 | 10:8009381 | CGTTTTCAGATCGAG[A/C]CAAGTGTGTGCTCTG | 83860 |
rs766491260 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929980 | GCCAAGGTGGAAGGA[C/T]TGTTTGAGCCCAGGA | 83860 |
rs766541303 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857215 | TTGGATACTAGTTTC[C/T]GAATACTGGAAGAAT | 83860 |
rs766557935 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996731 | CTCAGCCAGACTGGA[A/G]TACAATAGTGCAGTC | 83860 |
rs766594548 | in-del | -/TTTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886365 | CTGCATGTTCTTCAT[-/TTTC]TTTCTTTCTCTCACC | 83860 |
rs766607616 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891177 | TCCCATTGGTTGCTG[A/G]TATAATTATTATTTG | 83860 |
rs766610102 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943155 | GTAGCTCCGTGAGAC[C/T]CTGAGAACTCCACTC | 83860 |
rs766629730 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835500 | CCTTCATGTCAGTTT[C/T]CCTTTTTCTGGCCAG | 83860 |
rs766640500 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977654 | TTACTGCCACATTAC[A/C]CCCAGGTGGATGCAA | 83860 |
rs766657597 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931069 | AAAGCATCTAATACT[A/G]TAATAATAGTAACAT | 83860 |
rs766668369 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972838 | ATGTCAGTTTCCATA[A/T]AAACTAGTTAGCCTC | 83860 |
rs766735759 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917503 | AGGCAGGGGCCAGTT[C/T]CTATGGGGCCTTATA | 83860 |
rs766760178 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968590 | CAGTGAGTAATTACT[A/G]TGTGCCAAACACCAT | 83860 |
rs766770520 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858412 | ACCTCCTGGATGATA[C/T]AATCGTTTATGTCAG | 83860 |
rs766784532 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934908 | TGAAAATACATCAGT[A/G]AATAAAACCAAAGTC | 83860 |
rs766800556 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011457 | TTGTTTTTGGTTTTT[A/G]TGGAGATGATGTCTC | 83860 |
rs766824439 | snp | A/C | 5.04545e-05 | 0.00502242 | missense | TAF3 | GRCh38.p7 | 10:7965297 | AAATCAAAGAATTTG[A/C]AGATGTTGATCCCAA | 83860 |
rs766826582 | snp | C/T | 1.66277e-05 | 0.00288333 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964041 | TGAGAATTTCCTGGG[C/T]AAGAGACCACTGGAT | 83860 |
rs766832420 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951352 | TGCTGGACGAGGCTG[G/T]GATCACCCATACATT | 83860 |
rs766835923 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924003 | AGAAACAAAATTTCA[A/G]ACAGTTGAAGTCTGT | 83860 |
rs766840395 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931694 | ATTGTATGTTCTGCA[A/G]TTTTATTACGTAAAT | 83860 |
rs766855602 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999365 | AGCAACTATGGGCAA[C/T]GTATTTCTTTGAAAA | 83860 |
rs766867066 | in-del | -/AAAGAG | 1.68872e-05 | 0.00290574 | cds-indel | TAF3 | GRCh38.p7 | 10:7965251 | TGGAAGGAATTTCTT[-/AAAGAG]GAAGAGGCAGATCCC | 83860 |
rs766887299 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952490 | ACACGTTAGCCCAGG[A/G]TGTAGCCATAGAAAC | 83860 |
rs766914339 | snp | A/G | 3.31554e-05 | 0.00407144 | missense | TAF3 | GRCh38.p7 | 10:7964148 | TGTTATTGGAAGCTC[A/G]AGAGCCACTCAGCTC | 83860 |
rs766922649 | in-del | -/CA/TGTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858826 | GTGTGTGTGTGTGTG[-/CA/TGTA]TGCGCGCGCCTGCAT | 83860 |
rs766926357 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837957 | TAAAATAATGTTTGT[G/T]TATGTAAAAGCAGCC | 83860 |
rs766939871 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841032 | TTTTTGGTATTTTTA[A/G]TAGAGAGGGGGTTTC | 83860 |
rs766947779 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910069 | TAGGTTTTCATTGTT[A/G]TATTGTTACTTTTAT | 83860 |
rs766950049 | snp | A/C/G | 0.000366412 | 0.0135308 | missense | TAF3 | GRCh38.p7 | 10:7964606 | CAAATACAGACACCC[A/C/G]CTGATGCTGGGAAAC | 83860 |
rs766951410 | snp | C/G | 1.70737e-05 | 0.00292174 | missense | TAF3 | GRCh38.p7 | 10:7965095 | AAGTTGAAAAAGGAA[C/G]TAAAGACTAAAATGA | 83860 |
rs766956936 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903960 | TACGGTATTGTAGGT[A/G]TCTGGAAAACAGAGA | 83860 |
rs766972126 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879977 | AACTCTGGGAGTCTG[C/T]AGCAAGAGGAGCACT | 83860 |
rs766981281 | snp | C/T | 1.79922e-05 | 0.0029993 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009123 | GGCCAAGCCGGCGCC[C/T]TCGCAGAACAGGCCG | 83860 |
rs766993053 | snp | C/T | 1.6628e-05 | 0.00288335 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964776 | AGACATTTTTACTAG[C/T]CCTAAGAGAATTTCA | 83860 |
rs767097233 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935812 | TCTCATTGATTCAGG[A/G]GAAAAGTGCAACTGG | 83860 |
rs767110370 | snp | G/T | 3.58622e-05 | 0.00423436 | intron-variant | TAF3 | GRCh38.p7 | 10:8009028 | TAAGCACGGGTTTGG[G/T]TCGATGATGATCCTG | 83860 |
rs767119994 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003622 | ACCAACTTATAAGAA[A/G]CTATCATTTGTTGCA | 83860 |
rs767122364 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884672 | GGATTACAGGCGTGC[A/G]CCGCTGCGCCTGGCC | 83860 |
rs767123676 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945828 | CATTATCCCATTTTA[C/T]TGTCTCCCTAGCACT | 83860 |
rs767142436 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863843 | CAGTGCATCTCTTAT[A/G]CATAATTTATAAACT | 83860 |
rs767157004 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904796 | TTTTTCCAGATTCTC[C/T]GGAAAAACTGGAAGA | 83860 |
rs767165706 | in-del | -/AT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858736 | TCACATGCTTAGCAC[-/AT]GTTAGCAGCTATGAA | 83860 |
rs767167680 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873294 | GTTGAAATTGTGTTT[C/T]TCTCTAACAGACCTA | 83860 |
rs767180432 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992647 | ATAATGAATGCACAT[A/T]TTCCCCTAAGAAATT | 83860 |
rs767200014 | in-del | -/TAAAGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972262 | TGGTGAGCACACAGA[-/TAAAGT]TAATGGAAACAAAAA | 83860 |
rs767212199 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011556 | GCTGGGATTACAGGC[A/G]TGAGCAACCACGCCT | 83860 |
rs767212397 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861862 | TTCCAAACTGGAAAG[G/T]TTTTAGCTATTTATT | 83860 |
rs767223058 | in-del | -/TT/TTT/TTTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872213 | GAAGTGTTGGGTTGA[-/TT/TTT/TTTTT]TTTTTTTTTTTTTTT | 83860 |
rs767226140 | snp | C/T | 4.3757e-05 | 0.00467724 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014755 | CGAGCCCACTGACGA[C/T]TCCCGAGGGGCTGGA | 83860 |
rs767237968 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821176 | AGTTTCTTGGTTTCA[G/T]TGAGAATGAGATTGT | 83860 |
rs767252814 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985200 | TGGAACTGCCTCGCC[A/G]TGTTACCCCAGCTGA | 83860 |
rs767269625 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855705 | CTTACCAGACAAAGG[A/C]AGAAAACATCTGATA | 83860 |
rs767291376 | snp | A/G | 6.81083e-05 | 0.0058352 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818871 | CCATCGGTACTCTGA[A/G]CTCTGTGAGTACCGG | 83860 |
rs767292028 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987482 | CCAGTTTTCAAACAT[G/T]TAAGTTGTCAAAGGT | 83860 |
rs767298270 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012229 | CTCATGAAGAGAGAC[A/G]CTTTGTGGTTAGAGG | 83860 |
rs767300721 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923188 | ACATTCTATATCCTC[A/G]ATTCCTGGTATGTGA | 83860 |
rs767318898 | in-del | -/TGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978739 | TCTCTAAGAGGAAGA[-/TGT]TGTTATCCATCATTC | 83860 |
rs767344217 | snp | A/G | 4.48632e-05 | 0.00473599 | intron-variant | TAF3 | GRCh38.p7 | 10:8014629 | TCTGAGCTTGTTTTC[A/G]CGTGCAGGCCCTGTG | 83860 |
rs767360714 | snp | C/T | 3.33762e-05 | 0.00408497 | missense | TAF3 | GRCh38.p7 | 10:7965543 | GGGTCCCAGCCATGC[C/T]GCCATCTTTGTTGCC | 83860 |
rs767368825 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866976 | TTAAAGATATGATTT[C/T]GGCTGGGCGTGGTGG | 83860 |
rs767416385 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843347 | CTCCTGGGCTCAAGC[A/G]ATCCTCCCCACTCAG | 83860 |
rs767447072 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899902 | ATATTAGTGACTTTT[C/G]TAGATTATGGGGTTA | 83860 |
rs767459751 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958863 | CTTTTGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 83860 |
rs767481477 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988197 | CTGGGTAGGGTAGCT[C/T]ATGCCTATAATCCCA | 83860 |
rs767511734 | snp | C/T | 1.65619e-05 | 0.00287762 | missense | TAF3 | GRCh38.p7 | 10:7824398 | CATGAACTAGAAGAC[C/T]ATATTCACAACATTG | 83860 |
rs767518148 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929612 | CAAGTGACCTACTCA[A/C]CTCAACATCCCAAAG | 83860 |
rs767561698 | snp | C/T | 1.68377e-05 | 0.00290148 | missense | TAF3 | GRCh38.p7 | 10:7964442 | CCAAAGAAAAGAAAT[C/T]ACCTGGACGTTCCAA | 83860 |
rs767583692 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836902 | TTACCAAAAATACCT[A/G]TGGAGAGGAGTTTTC | 83860 |
rs767592113 | snp | A/G | 1.8248e-05 | 0.00302054 | missense | TAF3 | GRCh38.p7 | 10:7965656 | AAGAAGGAAAAAGAG[A/G]AGGAGAAGAAGGAGA | 83860 |
rs767618161 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818931 | CAAGGGTGACACCTT[-/C]CGCTCTCCCTGTCCC | 83860 |
rs767620638 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918681 | GACCCAGGCACTCAG[C/T]CTGAAGCTTAGCTAG | 83860 |
rs767621653 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886653 | TAACATATATACATC[A/G]TAGCACATAGCTGAC | 83860 |
rs767646603 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868001 | GAGAAAATGTATTTC[C/T]TGGTCATTGAGTGGA | 83860 |
rs767649557 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943147 | GGTTCCCTGTAGCTC[C/G]GTGAGACTCTGAGAA | 83860 |
rs767662923 | in-del | -/AAAGTG | 1.74114e-05 | 0.00295049 | cds-indel | TAF3 | GRCh38.p7 | 10:7965182 | AGTAAGGAGAAGGAT[-/AAAGTG]AAAGAGAAAGAGAAA | 83860 |
rs767672441 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010169 | ATTTCTGCCTCCCAA[A/C]GTGCTGAGATGACAG | 83860 |
rs767675013 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859707 | ATGGCTGCACTTTAT[C/T]TTACTCATTTAGTTT | 83860 |
rs767686295 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834791 | ACTGATACTATCATT[C/T]ATGATTACTGAAACA | 83860 |
rs767688607 | snp | A/T | 3.32353e-05 | 0.00407634 | missense | TAF3 | GRCh38.p7 | 10:7964297 | CCAACTGCAAAACCA[A/T]TAGAAACAAAGTCAT | 83860 |
rs767703108 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931902 | CAGAAATGAATTCAT[G/T]ACAATGTAATGTGGC | 83860 |
rs767707760 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972185 | TCCTTTTGTTTGTTG[A/T]TTTTGGTAAGTGCAT | 83860 |
rs767718232 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008484 | TGACAATGGCATTGA[A/G]AGTATTAAGAAGAAA | 83860 |
rs767725890 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858641 | TGCCTGTCAATATAT[C/G]TACTGTTAATGAGAA | 83860 |
rs767743363 | snp | C/G | 1.67061e-05 | 0.00289011 | missense | TAF3 | GRCh38.p7 | 10:7964970 | CTTCAAATATGCCCC[C/G]CAACTTTCCTTATAT | 83860 |
rs767744234 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974377 | TTTCAGTGTGATGAG[A/T]TGAAATACTTATAGG | 83860 |
rs767759478 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868036 | GGTCACCATAAAGTT[C/G]TTGATCCTTGTCATC | 83860 |
rs767788248 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851879 | AGCCTCAAACTCCCA[C/G]GCTTTAAGCAATCCT | 83860 |
rs767790198 | in-del | -/TGCAGCTCCT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999879 | AGACGCACTCGATTG[-/TGCAGCTCCT]TGATCTCACTCAGAG | 83860 |
rs767790745 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892335 | TGAGCTGCTGAGGAG[C/G]TTTCAGCTTCATGGA | 83860 |
rs767809674 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961681 | ACTCTGTCCTGTTTT[C/T]TGATCATCTGTATTA | 83860 |
rs767812342 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919575 | TCATAACCATGGAGC[A/G]TTGGTTCCAGGACCC | 83860 |
rs767815797 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948956 | AGCAAGTGTAGGAAC[A/G]GCTTCCTCAGAGGGA | 83860 |
rs767830318 | snp | A/T | 3.18883e-05 | 0.00399288 | intron-variant | TAF3 | GRCh38.p7 | 10:7963874 | CTTAGGTTTTGTTAC[A/T]TTCCAATAATATTTA | 83860 |
rs767830742 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839035 | TGGTGTTCAGTACAC[A/G]TGTCTTAGCATAAAC | 83860 |
rs767832369 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012618 | TACGGGTGACTGCTG[G/T]TTCTCACCCCTTGTT | 83860 |
rs767926544 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924187 | ATGTGGTGCCAGGGT[A/G]TTTGAGAAAGTGTGA | 83860 |
rs767927247 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835627 | GCCCCATTGGATCTC[A/G]CTCAGCCCCTTGTAC | 83860 |
rs767939279 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881459 | TAATCAAGTAAAAGA[C/T]ATTTGTCTCTCAGAC | 83860 |
rs767940712 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001583 | CCATATAAAATTGTC[A/G]TGCAGTCAAATCAGC | 83860 |
rs767943779 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000457 | GTTTGTTAATTATGG[A/T]TAAATCAAAAGGAGA | 83860 |
rs767950633 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825796 | GTGATTAATGCCGCT[A/G]TGAACATCGATGTGC | 83860 |
rs767965586 | snp | A/C/T | 0.000132495 | 0.00813829 | intron-variant | TAF3 | GRCh38.p7 | 10:8009379 | GACGTTTTCAGATCG[A/C/T]GACAAGTGTGTGCTC | 83860 |
rs768000726 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869386 | AAATGAGATCACACC[A/G]TATATTCTGTGCTCT | 83860 |
rs768026036 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889186 | AGTACTGTTCCTTCT[C/T]CTGCTCCAGCCTTTG | 83860 |
rs768036448 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942351 | GCTTTAATTAAATTT[C/G]ATTGGCTTATTTATA | 83860 |
rs768039805 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953991 | TCCACAGGTGAATGA[A/G]TGGATTAGTCCTAGT | 83860 |
rs768046580 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008288 | TTTTTTAGTAGAGAC[A/G]GTGTTTCACCATGTT | 83860 |
rs768057300 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827397 | AACAGTGGGCCAGGT[G/T]TGATGGCTTATGCAC | 83860 |
rs768063817 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842175 | TTTGTTTTTTTTTTT[-/G]GTTTTTTTTTTTTTT | 83860 |
rs768078802 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876693 | TATATTGTCCTAAAA[A/G]TCAGGAAAGTTCTTT | 83860 |
rs768103648 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995246 | GGTTATGTCATCAGC[G/T]TGATATACATTGAGG | 83860 |
rs768104064 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835364 | GAGATTCAGGGTAGC[C/T]CCTCTGACTTTGCAG | 83860 |
rs768113080 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997089 | AAATCTGAAGAAGAA[A/G]AGTAAGTTTTGGTGT | 83860 |
rs768125065 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911437 | GCAAGTCCTCTGCCA[C/T]ATGGCAGAGAAGCAG | 83860 |
rs768135486 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913921 | CTTGATCCAGAATGT[-/G]ATATTCTGCCAAAGC | 83860 |
rs768159123 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846537 | TTTTTGAACAGTTTT[A/G]ACTATTACAGTTTTG | 83860 |
rs768180246 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912301 | GACAGGGTCCCACGA[C/T]GTTGCCCAAGCTGGT | 83860 |
rs768186992 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875866 | CAGAAGGCAATAAAA[A/G]CAGCAAATTTTAAGA | 83860 |
rs768192682 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878662 | TATAGGAAATTCCCT[C/G]TCTAGATGCACTATA | 83860 |
rs768206021 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009867 | CTAAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 83860 |
rs768211944 | in-del | -/TGTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858808 | ACATTATAGGCTCTG[-/TGTG]TGTGTGTGTGTGTGT | 83860 |
rs768213937 | snp | G/T | 1.65798e-05 | 0.00287917 | missense | TAF3 | GRCh38.p7 | 10:7964139 | TAGATGTTGTGTTAT[G/T]GGAAGCTCGAGAGCC | 83860 |
rs768234421 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823129 | AAAAACGAACAAAAA[A/C]CAAACTTTTATGATC | 83860 |
rs768240631 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864773 | TTTCATTTTATTAAC[A/G]TTATCTTTCAAGAAG | 83860 |
rs768250638 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894917 | TTGAGACTCTGCCAC[A/C]CAGGCTGGAGTGCAG | 83860 |
rs768252337 | snp | C/T | 4.98012e-05 | 0.0049898 | missense | TAF3 | GRCh38.p7 | 10:7964240 | TTGGCACCTCCCTCA[C/T]CCGAGCCGCCAATGT | 83860 |
rs768273666 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949401 | GCCTGGGTGTCTTAT[A/G]TATAAGTGGACACAA | 83860 |
rs768284276 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920186 | TGAGTGCAGGTGATC[A/G]AGGCTGCAAGTGAGA | 83860 |
rs768301735 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858200 | GGCTGTTAAGAATCA[C/T]TGTCTTTTCCCAGAG | 83860 |
rs768316318 | snp | C/T | 0.000119386 | 0.00772521 | missense | TAF3 | GRCh38.p7 | 10:8009167 | CGGCCCCCGCGCCCG[C/T]CCCCGGCCCCATGCT | 83860 |
rs768319624 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996376 | TGTTTTATGACCTAT[C/T]CTTGGAGGTGACGTG | 83860 |
rs768325024 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938104 | CATTTTTTCAACAAA[A/G]TAAAACTTAGAGTCC | 83860 |
rs768336071 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922931 | TATTAGAAAACTTGT[A/G]TCTTCCAGATTCTAC | 83860 |
rs768344202 | snp | C/T | 1.68995e-05 | 0.00290679 | intron-variant | TAF3 | GRCh38.p7 | 10:7824278 | AATATATTCGTGGGA[C/T]TTCTTCAAATAATTT | 83860 |
rs768354042 | snp | C/T | 1.68371e-05 | 0.00290143 | missense | TAF3 | GRCh38.p7 | 10:7965278 | GCAGATCCCTACAAG[C/T]TTAAAATCAAAGAAT | 83860 |
rs768354092 | snp | C/T | 1.65858e-05 | 0.00287969 | intron-variant | TAF3 | GRCh38.p7 | 10:8013870 | CCTGCCGGCCACACT[C/T]ATTAGGCAGCATCAG | 83860 |
rs768360127 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003675 | CTTACACCATTATCC[-/A]AAAAAATCTTTTAAA | 83860 |
rs768363890 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946296 | TCAGACACAAAACTC[A/G]TTACGCAGTATGGCT | 83860 |
rs768374250 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009895 | AAAGTGTGGGATTAC[-/A]AGGCATGAGCCACCG | 83860 |
rs768386531 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982358 | CTTCCTAGCAGTAAG[A/G]GCAAAAAAATACATT | 83860 |
rs768398385 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912006 | CACTTTCGGATCATC[C/T]AGAATTCTGAAATCA | 83860 |
rs768404137 | snp | C/T | 1.65941e-05 | 0.00288041 | missense | TAF3 | GRCh38.p7 | 10:7964829 | AAGCTTCCACTTCCG[C/T]GAACAATTTCACAAA | 83860 |
rs768411811 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908179 | ACGTTTGTTCCAAAA[C/T]GAGTCACAAACTCAG | 83860 |
rs768433934 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955187 | CTTTTTTGTTTTTCA[A/G/T]CCTCTCTGCCCCACC | 83860 |
rs768437660 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983219 | CCTCCGTTATCAGCC[C/G]CCGTGAAGGACTTCG | 83860 |
rs768489286 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7835182 | TCTTTGGCCACACAT[-/A]AAAATACACTAACAC | 83860 |
rs768537394 | in-del | -/TACACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939577 | GAAATAGAAGAAAAC[-/TACACACA]CACACACACACACAC | 83860 |
rs768591337 | snp | A/C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973858 | GAGACAGCCAGGCAC[A/C/G]GTGGCTCACGCCTGT | 83860 |
rs768594779 | snp | A/C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931145 | TTAATCCACCTGCAT[A/C/G]GTAGTCAAAATGCAT | 83860 |
rs768612791 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987446 | ATTTTACTGTTGTAT[A/C]ATCATTTATCTTGCC | 83860 |
rs768622854 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898037 | CTTATTTTTTTCTCT[C/T]TTTATTATGTCTTTG | 83860 |
rs768628421 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942840 | TCTTAACTCTTAGAA[A/G]TGAATTTAAAATGTT | 83860 |
rs768636107 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845914 | CTTATGGTTGAAAAA[C/G]TTTGATTTCTGAGTT | 83860 |
rs768664847 | snp | G/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819539 | AGGGACCGTGGGCAG[G/T]TGACAAGATTCTCCA | 83860 |
rs768668124 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989098 | TCAAAGCATGTGATC[A/T]ACCAAGATTTCAACC | 83860 |
rs768691861 | in-del | -/AAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977616 | ACTTATCTGAAAAAT[-/AAG]AAACTCTGTACTGAA | 83860 |
rs768693552 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859401 | TTTCAGGAGGGCAGC[A/G]GGGATTTCTGAAATC | 83860 |
rs768695065 | snp | C/T | 6.61682e-05 | 0.0057515 | stop-gained | TAF3 | GRCh38.p7 | 10:8014740 | AAGAAGAGGAAGCAT[C/T]GAGCCCACTGACGAC | 83860 |
rs768696815 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817284 | TTGGGGACAGAGTGT[C/T]CAGGGAGTAAATGCA | 83860 |
rs768709590 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004889 | CCCCATTTTTCTTCT[A/G]GAATTATGATCAAAC | 83860 |
rs768710526 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845253 | ACCAAAAAAAAAAAA[-/T]CTCCCACTGGAATAT | 83860 |
rs768722232 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832353 | GAATTCCATCTATGT[A/T]GTCACAAATGACAAA | 83860 |
rs768740219 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872699 | AGTGTACTGCTTAAG[A/G]AAGCCACTGATCTAC | 83860 |
rs768744731 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862148 | AGTTCCATTTCTCTC[C/T]TGAGATTGCCAGTGA | 83860 |
rs768756278 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931724 | TTAGTTCTGGGTAGT[C/T]AATCAGGCAACAAGT | 83860 |
rs768768682 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7992012 | GGTGTATCTTTTATG[A/G]CTAACTTACAAATTC | 83860 |
rs768821143 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980691 | GTCCAGCCTAGCAGA[A/G]GCCTTGCCTTGATGC | 83860 |
rs768835925 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823703 | GTAGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 83860 |
rs768850526 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934374 | CTTAGATTCAATGAA[A/G]TGTGGTAGGCATTCC | 83860 |
rs768863523 | snp | C/T | 1.66101e-05 | 0.0028818 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964896 | CTCAAGTTCCGATAA[C/T]TCATGGACAATGGAT | 83860 |
rs768868589 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890989 | TTGCTAAGCATGTAG[C/T]TGAACTTGCGGATGC | 83860 |
rs768899564 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820536 | GTCTCACTCTGTCGC[C/T]GAGCGTGGAGTGCAG | 83860 |
rs768924784 | in-del | -/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853181 | AAAAATCATATAAAC[-/TT]ATAATTAAATAAATT | 83860 |
rs768925341 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016738 | TACTGAAATCAGAAT[A/G]GAGGTGCCTATATAT | 83860 |
rs768925718 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825125 | AGTTCCCTTTTTTCC[G/T]GCATAATTTTAGATG | 83860 |
rs768931998 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011071 | CAAACACACAACGAA[A/G]TATTTAAGGTGTGTG | 83860 |
rs768940315 | snp | A/C | 1.65614e-05 | 0.00287757 | missense | TAF3 | GRCh38.p7 | 10:7824355 | GGATGATGTTGGTGA[A/C]GCTTTCCAGCTGATG | 83860 |
rs768946102 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840358 | GGGGTTTCACCGTGT[C/T]AGCCAGGATGGTCTC | 83860 |
rs768953064 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939045 | ACCAGCCTGCAGAGA[A/C]GATTATGGGAAACAA | 83860 |
rs768973704 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849711 | GAGACAGTGTCTCTC[A/G]CTCTGTCACCCAGGC | 83860 |
rs769012904 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956468 | CTCCAGCCTGGGCAA[C/G]AGAGTGAGACTCCAT | 83860 |
rs769016928 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841610 | AGAGGAGATGTCACT[G/T]GAAGAGTCTTGATAA | 83860 |
rs769029089 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895932 | TGCCTTCAGTGAACA[C/T]CGAAGCTGACCATGC | 83860 |
rs769030252 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824517 | AGAGGAAAGAAAAGA[A/G]TACATTCCTGATTAC | 83860 |
rs769037793 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831021 | TTTTCACTTTTGTTG[G/T]TGTTAGCAGTGCTGA | 83860 |
rs769047026 | snp | A/G | 1.67309e-05 | 0.00289226 | missense | TAF3 | GRCh38.p7 | 10:7964579 | ATCAGTAAAGAGACT[A/G]TCCAGGTAAAACAAA | 83860 |
rs769062143 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944676 | ATCTCTTAGCTAATC[C/T]TCAAGTAATGGAATT | 83860 |
rs769066235 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832741 | TTTTAGTAGAGATGC[A/G]ATTTCACCATGTTGG | 83860 |
rs769066710 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891628 | TTATGTTTTTGTTAG[A/T]AACTTTTTTCTTAAG | 83860 |
rs769087533 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003938 | TTTGTCTTGGAAAAT[A/C]TAGTTATTTTCATAA | 83860 |
rs769087854 | snp | C/T | 1.91415e-05 | 0.0030936 | intron-variant | TAF3 | GRCh38.p7 | 10:7965766 | TTTCTCATTTTTGGC[C/T]CTATCTGAACAGAGT | 83860 |
rs769088663 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914225 | ATTAGAAATACGTAT[A/G]GAATTACTTACTGGT | 83860 |
rs769094288 | in-del | -/GT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957979 | TGACCAAATTTTGCA[-/GT]TTTATAATACACAGG | 83860 |
rs769099372 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855233 | GTGAGGGAGAGAAAT[A/G]GTTGAAAATCTGTTT | 83860 |
rs769100252 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002676 | CTGATTGAAGACAGA[-/T]TTTTTTTTAAATGTC | 83860 |
rs769119446 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950623 | TGAGTGTATATCCAT[A/G]TAGTTATATACAGTT | 83860 |
rs769131796 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837274 | AGGCTGAGGCAGGAG[A/G]ATTGCTTGAACCAGG | 83860 |
rs769154187 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866927 | AATTTTAGATCAATG[C/T]GCAATTTAAATTCCA | 83860 |
rs769186311 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940365 | TATTTTTAGCATGAT[A/G]CCATGCATATAATAA | 83860 |
rs769226546 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925300 | CCTCTGGCAGGTCAG[A/G]CGAGGCTCTGCCATA | 83860 |
rs769229636 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983296 | GTGGTAGGTTCCAGA[A/G]GGAAAGGAGGGCTCA | 83860 |
rs769240903 | snp | A/G | 4.96833e-05 | 0.00498389 | missense | TAF3 | GRCh38.p7 | 10:7824335 | GGCCGAACAGACCCA[A/G]TTTTGGATGATGTTG | 83860 |
rs769265049 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970719 | ACTTTAGCAATCAGA[A/G]CAATTAAAAATTTTA | 83860 |
rs769273907 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877958 | TAATGTTTCTGTCAC[A/C]TTACCTGTCACAGTG | 83860 |
rs769282803 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969626 | TTTATGTTAGTGGAA[A/C]TGGATGGTTATACCT | 83860 |
rs769291378 | snp | C/T | 1.90769e-05 | 0.00308838 | intron-variant | TAF3 | GRCh38.p7 | 10:8009360 | CCCGCGCGGTTAGCA[C/T]GGAGACGTTTTCAGA | 83860 |
rs769327523 | snp | C/T | 3.31603e-05 | 0.00407174 | intron-variant | TAF3 | GRCh38.p7 | 10:8013714 | CATTTTTGCCGCTTC[C/T]GCTTTGCAAACATCA | 83860 |
rs769336279 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822450 | GTTTTATTTATTTTC[-/T]TTTTTTTAATGCATC | 83860 |
rs769356881 | snp | A/G | | | missense | TAF3 | GRCh38.p7 | 10:7964097 | CCATGAAGCGGCCTC[A/G]GCTATTAAGCACTAA | 83860 |
rs769366221 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865698 | GCTTTCACAGGCAGG[A/G]GTGAAGGAAAAATAG | 83860 |
rs769387587 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908382 | AAAAATTGGAAAGTC[A/T]TATAATTAATCAAAA | 83860 |
rs769389459 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855375 | GTGATAACACACCAG[A/T]CCAGAAGGCAGGGAT | 83860 |
rs769415532 | snp | G/T | 1.69137e-05 | 0.00290802 | missense | TAF3 | GRCh38.p7 | 10:7965236 | GAAACAAAGTATCCC[G/T]GGAAGGAATTTCTTA | 83860 |
rs769419815 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931749 | ACAAGTATTAATACT[A/G]AGTGCTTATTTCATT | 83860 |
rs769423145 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939290 | ACACTGAACAGGTGA[C/G]ACTTTCCTCCCTTTT | 83860 |
rs769432245 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846699 | TCCACTGGACCTCCT[A/G]TAAAGCTAAGACATG | 83860 |
rs769434795 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909261 | TGGGTTTCTGAGAGG[G/T]CTCTAGTTGATTCTT | 83860 |
rs769437722 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984689 | AAACTTTCTCTCCGC[A/G]GTGTTATCAAGGTCC | 83860 |
rs769484891 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998850 | CTCAAAAAAAAAAAG[-/A]AAAAAAAAAGAAAGA | 83860 |
rs769507648 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911399 | GAAAAGTGAACACTT[C/G]CTTCTGAGTTTCATG | 83860 |
rs769507980 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921361 | TCTCACTTTTTAGTC[-/A]TCTATTACTTAGCCA | 83860 |
rs769524621 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893867 | TCCTTTAATATTTCT[A/G]TATACCCATATTCAT | 83860 |
rs769531880 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011591 | TATTATTAAATTTCC[C/T]TAAAGGAGTTTTGGA | 83860 |
rs769556732 | snp | A/C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837977 | TAAAAGCAGCCATCA[A/C/G]ATAATTTATCCTTGA | 83860 |
rs769572560 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912752 | AGATCCAGTTCAATG[A/G]TTCATTGCCAGTGGC | 83860 |
rs769593878 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889379 | TGTAAACACTTCACA[C/T]CTACTCATTTAATCT | 83860 |
rs769614853 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869695 | ATACATATTTCAGTT[A/G]CCCTCCAGAAAGGCT | 83860 |
rs769643220 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963462 | TGCTGTTACTGACTG[A/C]CACTCTTTTAAGAAT | 83860 |
rs769663269 | snp | C/T | 4.97508e-05 | 0.00498728 | missense | TAF3 | GRCh38.p7 | 10:7964121 | GCACTAAAGGGGACA[C/T]GCTAGATGTTGTGTT | 83860 |
rs769713258 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998032 | TGTTTTCGGTCATCA[C/T]AAAAATAACCTTAGC | 83860 |
rs769718277 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891996 | TTGCTGATAGTTAAC[-/T]TATGACCAATTTTCA | 83860 |
rs769724539 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859620 | TTTGCCCTCCATTTG[A/G]GAATGAAGTGAGGGA | 83860 |
rs769745057 | in-del | -/AAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975070 | ACAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 83860 |
rs769756682 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857695 | TTTTTTCTTTCACAC[A/G]GGTATAAATATCTAA | 83860 |
rs769766088 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933222 | CTGTAGGAATGCAAA[C/T]GCTATGGCATTTTGC | 83860 |
rs769771292 | snp | C/G | 7.18675e-05 | 0.00599404 | missense | TAF3 | GRCh38.p7 | 10:8009108 | GGTCCCTGCCCCCGA[C/G]GCCAAGCCGGCGCCC | 83860 |
rs769793309 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876919 | ATCACTTGTACTTTG[A/T]TTTGCTGCCTTTATC | 83860 |
rs769793487 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890533 | GCATTTTGTTTTAAG[A/T]TGTATAAATATGTGC | 83860 |
rs769794259 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949615 | GAATTTAATAGTAAC[C/T]TGAAACAACTGTAAA | 83860 |
rs769798883 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984599 | TTATCCTTAATGGGT[-/C]CAGGTCTTATTAGTT | 83860 |
rs769816799 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847975 | GGGTTTCACCATGGT[G/T]TCCAGGCTGATCGCA | 83860 |
rs769844184 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012944 | TTGCTGGTGTTGAAT[A/G]CCCATCAGTGAATTA | 83860 |
rs769849577 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821636 | TCCAAGCATTCAAGG[A/G]CAGATGTCTCTGTCG | 83860 |
rs769852104 | in-del | -/TACAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898381 | GTGAAACCCCGTCTC[-/TACAAAAA]TACAAAAATTAGCTG | 83860 |
rs769857864 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935562 | GCACTCCAGCCTGAG[C/T]GACAGAGAGAGACAA | 83860 |
rs769871274 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982978 | CTGTGTTAATCAAGA[C/T]TCTTGGTGGCAAGTA | 83860 |
rs769884521 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905523 | TACAGCCCATTTTTT[G/T]AGTGTTTTTAATGAA | 83860 |
rs769918295 | snp | G/T | | | missense | TAF3 | GRCh38.p7 | 10:7965560 | CCATCTTTGTTGCCA[G/T]TGCTTCCGGAAAAAC | 83860 |
rs769930137 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980628 | ACCCTGAAATTACAG[C/T]CTCAACACCTAGAGA | 83860 |
rs769941379 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012261 | CAAAATTTATGATTT[A/T]GATGACATACAAAGG | 83860 |
rs769959746 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892008 | AACTTATGACCAATT[C/T]TCATTAACAGATAGA | 83860 |
rs769982394 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888390 | TTTATCTAAATTTAT[-/A]AAAAAAAAAGTTTCT | 83860 |
rs769998986 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843972 | TTTCAATTTCTGTTA[A/G]TGTTAATGAATATCC | 83860 |
rs770012895 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7893068 | CCGTTGATCCACCCC[C/G]CTTGGCTTCCCAAAG | 83860 |
rs770029239 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922383 | ATTGTGAATGTTGTA[C/G]TGTCTTAATCTCATT | 83860 |
rs770047577 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911034 | CTTAGCACTAAATGA[A/G]ATGTATGTGTTGGGG | 83860 |
rs770050790 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852392 | GTGACTGGTTGATCT[C/G]TCTCCCTCTCTCATT | 83860 |
rs770053914 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923855 | AGAAAGCAAGGCAAG[A/G]TATCTTAAGAAATTT | 83860 |
rs770057733 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916228 | ATTATTACATTATGT[C/G]TTTGTCTGAATCTCC | 83860 |
rs770067084 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957459 | CCAAGGCATATCTCT[A/G]TTATTGATGGGTATT | 83860 |
rs770080529 | snp | A/G | 3.14956e-05 | 0.00396822 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818826 | CACGGACGTGCTGCA[A/G]CGCTATCTGCAGCAG | 83860 |
rs770097793 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929068 | CAGTATTTTAGGTTT[A/G]GTTTTTAAGGGAGGT | 83860 |
rs770102932 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838793 | TAAGGATCTGGCTGC[C/T]TCTCTCTTGGCCCTC | 83860 |
rs770118422 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872861 | TGTTATATAAAATAA[C/T]ATTAAATGTGCATTC | 83860 |
rs770123211 | snp | A/G | 1.88677e-05 | 0.0030714 | missense | TAF3 | GRCh38.p7 | 10:7965732 | AGAAGGAGAAACACA[A/G]GCATGAAAAAGTAAG | 83860 |
rs770138323 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826616 | AATAACAAATCTTGA[C/G]AACACTACTTTTCAC | 83860 |
rs770162910 | snp | C/G | 1.66084e-05 | 0.00288165 | missense | TAF3 | GRCh38.p7 | 10:7964805 | CAGGCCCGGAGTGTA[C/G]TACTCCCAAAGCTTC | 83860 |
rs770174417 | snp | A/G | 3.38558e-05 | 0.00411422 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965601 | GAAAGAGAAGGTGAA[A/G]GAGAAAGAAAAGAAA | 83860 |
rs770192588 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820613 | GATCCTCCCGCCTCA[A/G]CCTTCCAAGTAGCTG | 83860 |
rs770193275 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004109 | AGGCTGGAGTGCAGT[A/G]GCATGATCACGGCCC | 83860 |
rs770199007 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856428 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 83860 |
rs770211979 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880829 | TGCGTGCAACAGATG[C/T]ATATTTAAACGATAT | 83860 |
rs770222918 | in-del | -/GATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951927 | ATTGTTTCACTTTCT[-/GATA]GATAAATGGCTAATT | 83860 |
rs770227071 | in-del | -/GTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920302 | AATTTAAACATACGT[-/GTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTATGTGTG | 83860 |
rs770241184 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886586 | GAAATTTCTTTATCA[C/G]TTAGATGAGGGTAAT | 83860 |
rs770278467 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826262 | CAAAACTAGGACTTT[A/G]ATCATAATCTACACT | 83860 |
rs770299219 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007455 | GGGCAGTGGTTGCTC[G/T]GGGGCAGGGAAGGAA | 83860 |
rs770309149 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910633 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 83860 |
rs770313153 | in-del | -/AGATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869183 | ATAAAAAATGTTTAC[-/AGATA]AGATAAAAGAAAGAT | 83860 |
rs770349127 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957932 | TGCAATAACATATCA[A/G]GATTAGATATCTTGT | 83860 |
rs770349611 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862251 | GATTGCCTTTCTCTT[C/T]AGTATGGATCAAAGT | 83860 |
rs770350232 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993118 | CCAAACCAGACTTAT[A/G]TCTCATAAGGACTTG | 83860 |
rs770404019 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945706 | CTTGTTCATGACATC[A/G]TCACACAGCTGGTCT | 83860 |
rs770404138 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959600 | TTTTTTTTACTGAAA[C/T]ACAAACAACCATCAT | 83860 |
rs770455280 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946280 | TGCTCCTTCCCATGC[C/T]TCAGACACAAAACTC | 83860 |
rs770490490 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985929 | GCTGGGACTATGGGC[A/G]CCCGCCCCCACACCC | 83860 |
rs770492572 | snp | A/G | 1.66338e-05 | 0.00288386 | missense | TAF3 | GRCh38.p7 | 10:7964918 | ACAATGGATGCCTCC[A/G]TTGATGAGGTTGTAC | 83860 |
rs770534289 | snp | G/T | 0.000153926 | 0.00877151 | intron-variant | TAF3 | GRCh38.p7 | 10:8009352 | ACCTGCCGCCCGCGC[G/T]GTTAGCATGGAGACG | 83860 |
rs770540237 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844553 | AGCTAATTTTTTTGT[A/G]TTTTAGTAGAGATGG | 83860 |
rs770562209 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907537 | AATAAAGGGATAACA[A/G]AGAATTCAGATGTCA | 83860 |
rs770574920 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920460 | TATGCTTTGCATTTT[G/T]TTCTGCAATTTAAAT | 83860 |
rs770579880 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886535 | TTCTAGCTTTGCCAC[A/G]TTGTGGCTATATGAC | 83860 |
rs770581955 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897411 | AAATTCTGATCCGTT[C/T]TGAATCCCAATCCTA | 83860 |
rs770585029 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836266 | AACCAGTTGCAGTTG[C/G]CCATTTCCACGTTTT | 83860 |
rs770611159 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916539 | ATAATAACTAACATC[A/G]TGTTTAACACATAAT | 83860 |
rs770616213 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845716 | ACTCCGTGTGGCTGT[A/G]TAATCTCAGCATCAT | 83860 |
rs770625707 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009992 | TCTCGGCTCACTGCA[G/T]CCCCTGCCTCCCAGG | 83860 |
rs770642483 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959867 | TAAAGCAGACCTTAC[A/G]TCCATAAGACTTGAA | 83860 |
rs770654056 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934147 | GGAAGAATTAGAAAC[C/T]GAAAGGAAAGAACTT | 83860 |
rs770654998 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930312 | GGAGGAAAAAGAGAA[A/G]TACTTACTTGAATTA | 83860 |
rs770667072 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857655 | TGAAAGGGTAATTGT[A/G]TTTTGATTTGAGGGA | 83860 |
rs770715467 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957630 | CAATCAATTTTTTAA[A/T]TTTTTTTTTCAATAT | 83860 |
rs770717444 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840525 | TAGGCATCCAGAATG[-/A]AAAAAAAAAAAAAGA | 83860 |
rs770740115 | in-del | -/TTTTTCTTCC | 2.95051e-05 | 0.00384079 | intron-variant | TAF3 | GRCh38.p7 | 10:7963892 | CCAATAATATTTATT[-/TTTTTCTTCC]TTTTTCTTCCTTTAC | 83860 |
rs770756091 | snp | A/G | 1.65916e-05 | 0.00288019 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964092 | GCCAGCCATGAAGCG[A/G]CCTCGGCTATTAAGC | 83860 |
rs770790970 | snp | C/G | 5.03537e-05 | 0.0050174 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965034 | ACCTCTCCACAAGGT[C/G]TATGAGGAGAAAACC | 83860 |
rs770806012 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010943 | AATCCCACCATGTCC[A/G]CTGAGTCCACATTGT | 83860 |
rs770809502 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011898 | TGGAAAGCTTACTGG[C/T]TGTGCATGGTGTCTC | 83860 |
rs770847843 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870215 | AATCATAAAACTCTG[A/G]TCCCAAGTCCATCAT | 83860 |
rs770857426 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998747 | AGGAGGCTGAGGCAG[C/G]AGAATTGCTTGAACC | 83860 |
rs770857724 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848203 | TTCTTCCTGATATAC[A/T]GAGGGTTAAAGTAAA | 83860 |
rs770860100 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974959 | GCTGCCTGTAATCCC[A/G]GCTACTCTGGAGGCT | 83860 |
rs770864586 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984870 | TTATAATTTCTCCTA[A/G]AGATCAAACTACTCA | 83860 |
rs770881016 | snp | A/C | 1.67657e-05 | 0.00289527 | missense | TAF3 | GRCh38.p7 | 10:7963987 | GCAGGTTCCCTTGGA[A/C]GAAGATGATGAATTG | 83860 |
rs770894387 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922101 | TAATAAATTCAACTC[C/T]CAGTATTCAAACTCG | 83860 |
rs770907846 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858207 | AAGAATCACTGTCTT[C/T]TCCCAGAGAATTTTT | 83860 |
rs770915557 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920300 | AAAATTTAAACATAC[-/GTGTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTATGTGTG | 83860 |
rs770919387 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963606 | AGTGGGAGTTGAACA[A/G]TGAGAACACATGGAC | 83860 |
rs770927718 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935628 | TAAAGCTAAGTAGAG[C/G]GCCAGAGAATACTGG | 83860 |
rs770928916 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840046 | TTTCCAATGCTATAG[A/T]AAGAGATTTTTGGAT | 83860 |
rs770929876 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962111 | CTCCCTCGGCCTCCC[A/C]AGATGTTGGCATTAC | 83860 |
rs770951368 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909336 | TCAGGAGGTGGAGGC[C/G]AGCTTAAGAAACCAC | 83860 |
rs770952441 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839627 | CACAGATAGAAGAAC[A/G]AAGGCTTGTATTGTG | 83860 |
rs770953640 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894445 | TGGTGGAGAGGTGGT[A/T]TCCATGTCTTCATCC | 83860 |
rs770956189 | snp | C/T | 1.66239e-05 | 0.00288299 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964683 | GATTGAGGCCTCTAT[C/T]GATGCTGTGATTGCA | 83860 |
rs770961063 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014489 | TAGTCCGCATGCCCA[A/G]CAATAGTGCTACACA | 83860 |
rs770974131 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950863 | TTGTGTTTAAAATGG[C/T]CCCAAAGCATAGTGC | 83860 |
rs771001353 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852533 | ATGGTTTTGTTTCAC[A/G]TGGTCCTCTGTTTAT | 83860 |
rs771016199 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002416 | CATGTCATCTGGAAA[A/G]TTACTACTTTCTGGA | 83860 |
rs771045895 | in-del | -/AGAGAA | 1.83859e-05 | 0.00303193 | cds-indel | TAF3 | GRCh38.p7 | 10:7965679 | GAAGGAGAAGGAAAG[-/AGAGAA]AGAGAAGAGAGAGCG | 83860 |
rs771065996 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882358 | GAAGTCAGTCTCTCA[A/G]TAGGATCTTAGAGGT | 83860 |
rs771068739 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967893 | CCTTGGCATTCTTTG[A/G]AATATTAGCCCTTGA | 83860 |
rs771076513 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924959 | TTTCCTGATACCTTA[C/T]CTTACTACTGTTTCA | 83860 |
rs771116832 | snp | A/C/G | 8.34821e-05 | 0.00646026 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7977270 | AGTCGCTCTGGCCCC[A/C/G]AGTCCAGTTATCCCC | 83860 |
rs771178698 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902799 | ATTATACTTGTGGCT[C/G]TAGAATGTTGATTTT | 83860 |
rs771191621 | in-del | -/ACTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826472 | TTGTGTTGTTTTGAT[-/ACTG]ACTTCTGGCTGAAAT | 83860 |
rs771211522 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976693 | AGACATGAGCCACCA[-/C]ACCCTGCTTGTTTTT | 83860 |
rs771224669 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946044 | TGACTGTCCTCCTGC[C/T]TTGGCCTCCTCTGTG | 83860 |
rs771231062 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875330 | ATGACGTTCTTTGAG[C/G]CTTTGGCTTATTAAT | 83860 |
rs771231624 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855775 | AACAGTCATGCAAGA[A/G]GAATTAATTTGAAAT | 83860 |
rs771236149 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987946 | TTCATTAAGTGCACT[A/G]CTCATGTGAACATAA | 83860 |
rs771238322 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917810 | TTGAAGTTATATAAG[A/T]TGAAAACTGAAAATG | 83860 |
rs771238523 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904721 | GTAGTGTGCACAGCG[C/T]TGGCTTTCATGATAT | 83860 |
rs771265876 | snp | A/T | 1.65405e-05 | 0.00287576 | missense | TAF3 | GRCh38.p7 | 10:8014675 | CACCCCCAGAAGAGA[A/T]GCAGTGGTTCTGCCC | 83860 |
rs771299336 | snp | C/T | 3.59131e-05 | 0.00423736 | missense | TAF3 | GRCh38.p7 | 10:8009101 | GCAAGGTGGTCCCTG[C/T]CCCCGAGGCCAAGCC | 83860 |
rs771302948 | snp | C/T | 3.33183e-05 | 0.00408143 | intron-variant | TAF3 | GRCh38.p7 | 10:8013882 | ACTCATTAGGCAGCA[C/T]CAGCCGCTCCTGAGA | 83860 |
rs771305228 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874385 | TTAAGACAATCATTT[C/T]TTGAAGTTATATATA | 83860 |
rs771358585 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946850 | ACAACTTTTTTTGTA[C/T]ATTTGATGCTTTTCT | 83860 |
rs771366796 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834028 | TTGTTTGGGTTCCTT[A/G]TATATTTTGCCTTTT | 83860 |
rs771368706 | in-del | -/CAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865482 | AGACTCCGTCTCAAA[-/CAAA]CAAACAAACAAACAA | 83860 |
rs771375897 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863556 | CGGAGGTTGCAGCGA[A/G]CTGAGATCGCCCCAC | 83860 |
rs771395486 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896284 | TCCGTGAATGGGGGG[-/A]AAACGTAGACCAAAA | 83860 |
rs771396562 | in-del | -/CAGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983175 | GATTCTTGGTGCTCA[-/CAGT]CCCTGGCGAAGCCCC | 83860 |
rs771401735 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973111 | TCTGAGCTCTTACAT[A/G]GGAATAACACCATCC | 83860 |
rs771436014 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985806 | TTTTTTTTTTTGAGA[C/T]GGAATCTCACTCTGT | 83860 |
rs771446340 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865816 | AAGGACTCTCCCGTC[-/A]ACCTCCCCTATCCAT | 83860 |
rs771467477 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844404 | TTTTTTTGAGACGGA[A/G]TCTTGCTCTGTCACC | 83860 |
rs771467617 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866765 | AGCCCAATTAGAGGC[A/G]AGTGTTAGGAAAACC | 83860 |
rs771470584 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981873 | TATATAATGAAAATG[A/G]GAGCTAAAGCTTTGC | 83860 |
rs771491582 | in-del | -/AAAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898547 | CAAGACTCTGTCTCA[-/AAAAAAAAAA]AAAAAAAAAAAAAAT | 83860 |
rs771504771 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888142 | CAGATCTCTCCCATA[C/T]GAAACGTTTAAAGTT | 83860 |
rs771553054 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935682 | GGGAAGGGGGCTCTG[A/G]TAAGTGAGAATTAAA | 83860 |
rs771555041 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900770 | AGGGTAGTGTTTCAC[G/T]GTTTTACTGAACTTT | 83860 |
rs771563922 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852439 | CTCTTTCCCTTTTAC[A/G]TTTTCATATTTGTTG | 83860 |
rs771583788 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995265 | TATACATTGAGGTTC[A/G]TTCATTTCATCTAGT | 83860 |
rs771595506 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822041 | GTTATGGAAGGACTT[A/G]AAAGCTAGACAAAAG | 83860 |
rs771607891 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936805 | ACAGACTAGTTGTAC[A/T]GCTATCAACATCCTC | 83860 |
rs771610820 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822147 | AATTGTACTGACAGT[A/G]ATGTGCATAAGAGAT | 83860 |
rs771624699 | snp | C/G | 2.22963e-05 | 0.00333881 | missense | TAF3 | GRCh38.p7 | 10:8009184 | CCCGGCCCCATGCTC[C/G]TCAGCCCTGCGCCCG | 83860 |
rs771624761 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960102 | CCTAAGCCAAACCTT[C/T]ATCATTCTGTTTTGG | 83860 |
rs771639330 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973736 | TATTTGTTTATTCTT[C/T]CACAGATAACACAGA | 83860 |
rs771642188 | in-del | -/GTGA | 3.3222e-05 | 0.00407553 | intron-variant | TAF3 | GRCh38.p7 | 10:7824565 | TTCTCAAGAAGGTTT[-/GTGA]GTGTTTCTTCTTCAT | 83860 |
rs771728839 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874812 | GAAAACTTTTTTCAT[C/T]GATTTCTTAGCTGTA | 83860 |
rs771735563 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867598 | CTGAATATGGAGGAG[A/G]CAGGTACTCACTCAT | 83860 |
rs771739923 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879379 | TACTCATGCATAATT[A/G]ATTATATATTTTATC | 83860 |
rs771748344 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931678 | TATGTTTTCAAATCT[C/T]ATTGTATGTTCTGCA | 83860 |
rs771749858 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998987 | ACAGAACAAAGCCTT[A/C]AGGATCTGATTGTAC | 83860 |
rs771765717 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906061 | GGATAATTAAAAGTG[C/T]TCGTGGATAACACTT | 83860 |
rs771781933 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875681 | TTAAAAACCAGAACA[A/G]TGGTCCTTTTAAAAT | 83860 |
rs771792110 | in-del | -/ACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939578 | AAATAGAAGAAAACT[-/ACACACAC]ACACACACACACACA | 83860 |
rs771800918 | snp | G/T | 1.65655e-05 | 0.00287793 | missense | TAF3 | GRCh38.p7 | 10:7824527 | AAAGAATACATTCCT[G/T]ATTACCTGCCACCCA | 83860 |
rs771806423 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993381 | ATGGGGTCTTGCTGT[A/G]TTGCCCAGGATGGTC | 83860 |
rs771809026 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923738 | AAAAGGACTCCCCCA[A/G]TTTTTTGGATAACTA | 83860 |
rs771809703 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985781 | CTCATTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 83860 |
rs771822136 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966650 | CCTCTAAAAGTTATC[A/T]TCTTTGAGCTTGGCC | 83860 |
rs771833816 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820970 | TAGGCTAGGCATAGT[C/T]CAGATTATGTTTGCT | 83860 |
rs771877851 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834897 | GATCATATAGCTACT[A/G]TCTTGAGTTCTGCTA | 83860 |
rs771879734 | snp | A/G | 1.66424e-05 | 0.0028846 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964362 | AGGACAGAAGACTAA[A/G]TCACCTAAAACCGCC | 83860 |
rs771912809 | in-del | -/AG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867301 | AAAACCACCAAAAAA[-/AG]ATGTGATTTTTAAGT | 83860 |
rs771914191 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980455 | AACATTCCTGGAAAC[-/TG]TATTCTAAAGGAGTC | 83860 |
rs771921685 | snp | C/T | 1.66275e-05 | 0.00288331 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964911 | CTCATGGACAATGGA[C/T]GCCTCCATTGATGAG | 83860 |
rs771927458 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986237 | TATGCAATGATGATT[-/C]CCATTTCTTTATTAC | 83860 |
rs771938619 | snp | C/T | 6.71006e-05 | 0.00579187 | missense | TAF3 | GRCh38.p7 | 10:7965024 | CCACTCCCGAACCTC[C/T]CCACAAGGTGTATGA | 83860 |
rs771943432 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988752 | GATTCTGTCTCTCAG[-/A]AAAAAAAAAAAAAAA | 83860 |
rs771952972 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999853 | TCTGCTATGGATGAT[G/T]CACTCAACTTAGACG | 83860 |
rs771967427 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966297 | TCCGTTTTCTGCTTT[A/G]ATAAGATAAGGGCAC | 83860 |
rs771989987 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012015 | GACCCCATCTCTGCA[C/G]AAAATACAAAAATTG | 83860 |
rs772009906 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985993 | TTCGCCTTGTTGGCC[A/G]GGCTGGCCTCAAACT | 83860 |
rs772015123 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972017 | GAAGCTTAGTAATCC[A/G]CTGTAAATGCTCTTC | 83860 |
rs772028213 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840267 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCTGAATA | 83860 |
rs772055614 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952345 | CAAGAAGAGTGATTA[A/G]CGATAGCAATTTATT | 83860 |
rs772067011 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870381 | CTCCATTTTTACTTA[C/T]AGTTAATTCTCTGCT | 83860 |
rs772082684 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954555 | AGTTCTAGTTAACAC[-/A]GAGCTCTCCATAGTG | 83860 |
rs772102254 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897675 | CTTTCTTTCTTTCTT[C/T]CTTTTTTTTTTTTTT | 83860 |
rs772111501 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856012 | AGATAACCAGGAAGC[-/A]AGAGCAGGGTGCTAT | 83860 |
rs772112828 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940690 | CCAGGCATGGTGGCT[C/T]ATGCCAGTAATCCTA | 83860 |
rs772128801 | in-del | -/ACACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006182 | TGAAAAAAAAAATAC[-/ACACACAC]ACACACACACACACA | 83860 |
rs772134091 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990800 | GGAGCACAGGAGGTG[C/T]GTTAGAGAGTCCTGC | 83860 |
rs772150083 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894582 | TGTTTGAAGTTGGAA[C/T]TCATTTTCTGGGAAC | 83860 |
rs772152880 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977496 | TCTTTCACAGAGTAA[A/C]TGCTTTTTGCTTTAT | 83860 |
rs772156893 | in-del | -/TTCGATGATGATCCTGTT | 1.79306e-05 | 0.00299416 | intron-variant | TAF3 | GRCh38.p7 | 10:8009028 | TAAGCACGGGTTTGG[-/TTCGATGATGATCCTGTT]TTGACTTTTACCTTC | 83860 |
rs772163945 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941745 | TACTTGAACTGGGTG[G/T]CAGTGTTGAGGAAAA | 83860 |
rs772167306 | snp | A/T | 0.000155581 | 0.00881853 | intron-variant | TAF3 | GRCh38.p7 | 10:7975101 | AAAAAAAGAGTGAGA[A/T]GAAAATAATTCGTGG | 83860 |
rs772176969 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003805 | AATCCCAGCTATTAG[G/T]TAGGCTGAGGCAGGA | 83860 |
rs772183588 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976778 | TGAATGGTACAATTA[C/T]ACTTAGTATTTCAAC | 83860 |
rs772200494 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901929 | AATCTTATCATTTTG[A/C]CACATTGGCTTTCTT | 83860 |
rs772244565 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903084 | AAAGTTATCCTGGCA[C/T]GGTGACACACCCGTG | 83860 |
rs772260371 | snp | C/G | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819343 | TCCTAACTACATAGA[C/G]TCGTTGACAGCTCTG | 83860 |
rs772269094 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903309 | GGCCCCTACAGGTGA[A/C]CCCTGTGTCCTTTGA | 83860 |
rs772270551 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916751 | TATGTATAAATGTGG[A/C]TGGTTATATATCTTG | 83860 |
rs772285894 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975435 | GCAGTAAGCAAAACG[C/T]GCATGGTCCCTGCCC | 83860 |
rs772286708 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914210 | TAAAATACCTTTTCT[A/G]TTAGAAATACGTATG | 83860 |
rs772307806 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945554 | ACACTCTCTAGATGC[C/T]GCAGGGAGGCCAGGC | 83860 |
rs772309838 | snp | A/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818094 | TTGGACTTTATTTAA[A/T]CTTTGCAGTGGCAAG | 83860 |
rs772320851 | snp | A/G | 1.70356e-05 | 0.00291848 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7963960 | TGATGGAGGCACATC[A/G]GCAGAAGCCATGCAG | 83860 |
rs772370505 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883632 | TTATTCCTAATAGTT[C/G]CTGGATGGTAAATTT | 83860 |
rs772375364 | in-del | -/AG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838405 | GTTTGTTTTTGAGAC[-/AG]AGTCTCACTCTGTTG | 83860 |
rs772396408 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889659 | CTGGGCAAATTCCAC[C/G]TCTTAGTTATTCTTC | 83860 |
rs772406989 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830566 | TCGGCTCACTGCAAA[C/T]TCCACCTCCTGGGTT | 83860 |
rs772414686 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823029 | AAGGTAGGAGGATGG[C/T]TTGAGCCTGGGAAGG | 83860 |
rs772441798 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894495 | CGTCAGTGACCTGAT[C/T]GATTCCTAGATGGTG | 83860 |
rs772443349 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852737 | TCAATAGAAGTTGCA[A/G]ATTGGTAACAGTCTA | 83860 |
rs772445844 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013356 | TAACTTTCAAAAAAT[C/G]AGTTGTTACCACCCT | 83860 |
rs772461410 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861200 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGTCTT | 83860 |
rs772467137 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955542 | TTTTAAAGTTGCATG[C/T]GTCTGTGTAGTTAGT | 83860 |
rs772472021 | snp | G/T | 5.75656e-05 | 0.00536465 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818769 | GCAGATCTGCCAGGC[G/T]CTGGGCTGGGACTCG | 83860 |
rs772498798 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014804 | GGCTTCTTCCCTGGC[A/G]CCTCTGGAAGGGAGC | 83860 |
rs772509239 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853911 | TAAGTTTTGGAAATA[C/T]CAATAAAAACATCTG | 83860 |
rs772521859 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882679 | TATCAGAAGGCAGTG[A/G]GCAGTAAGATCACTC | 83860 |
rs772569329 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986581 | GTTTCCCAAGCTGAA[C/T]AAAACCAAGGAAAGG | 83860 |
rs772601047 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847316 | CTAGTCATTCAAAAG[G/T]ACTTTATCATGCAAT | 83860 |
rs772628066 | snp | A/C | 1.66001e-05 | 0.00288094 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964842 | CGCGAACAATTTCAC[A/C]AAGTCAGGATCCACT | 83860 |
rs772628421 | snp | A/G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982053 | TTTATATTTTAAAAT[A/G/T]TAGCCAGATTTAGCC | 83860 |
rs772631775 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895843 | AGTTTTTCTGGCGTT[C/T]AGTAGGCATTCACCA | 83860 |
rs772647888 | snp | G/T | 8.11129e-05 | 0.00636788 | missense | TAF3 | GRCh38.p7 | 10:8009188 | GCCCCATGCTCGTCA[G/T]CCCTGCGCCCGTGCC | 83860 |
rs772691733 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925119 | TACTGGCAACTTAAC[A/G]AGTTTTCTGTGAACC | 83860 |
rs772703091 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925441 | AGGTGTTAACCTCTT[C/T]TATAAACATGGAGTG | 83860 |
rs772725054 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933781 | AAAGAATGTACAATA[-/T]TATAGACTATGAAAT | 83860 |
rs772739819 | snp | C/T | 5.45004e-05 | 0.00521989 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009267 | CCCGGGTCCCGCCGC[C/T]TCCGGGGCCAGTGCC | 83860 |
rs772749645 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987208 | GTGCCTTTAGTCCCA[C/T]GTACTCAGGAGGCTG | 83860 |
rs772755632 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983306 | CCAGAAGGAAAGGAG[A/G]GCTCACACCAGAATA | 83860 |
rs772773997 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855434 | GGAATGTGAATACAC[C/T]GGATGCCGAGATGTC | 83860 |
rs772808015 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847801 | AGACAAGAGTTTCGC[C/T]CTGTCTTCCAGGCTG | 83860 |
rs772818386 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980778 | TGGGATCCTGAGGTC[C/T]CACTTGGACTTGGGG | 83860 |
rs772825336 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866928 | ATTTTAGATCAATGT[G/T]CAATTTAAATTCCAA | 83860 |
rs772833476 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009916 | TGAGCCACCGTGCCC[A/G]GCTTTTTTTTTTTGA | 83860 |
rs772849358 | in-del | -/TTTT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860805 | TTCTTTCTTTCTTTC[-/TTTT]TTTTTTTTTGAAATA | 83860 |
rs772864665 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929230 | TCTTCATTTGTGTTA[A/G]TTGAGAGAAGTAGTT | 83860 |
rs772886323 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871762 | GATTGCTATTTTGAC[A/G]TGACATTATATGCAT | 83860 |
rs772899500 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903618 | TTGGAATTGCTTAGC[C/T]GATGCAGTTTAGCAT | 83860 |
rs772927191 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896008 | ATAGTAAAATATATA[C/T]GAGTAGCAGGAGTGG | 83860 |
rs772935647 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962427 | CACACGTTTTTCTCT[C/G]TTGTCTAAAATCCTT | 83860 |
rs772939969 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933265 | CAGCTCACTGAACAT[A/G]CAAGTGTTTACATGA | 83860 |
rs772940375 | in-del | -/AAAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898551 | GACTCTGTCTCAAAA[-/AAAAAAAAAA]AAAAAAAAAAATCGA | 83860 |
rs772960465 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836145 | TACTATGTTTCTCAC[A/G]TTACTTAGTTTCAGA | 83860 |
rs772980542 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896564 | TGTAACCTCTCATTC[G/T]ACAGTCGCATTTGGG | 83860 |
rs772980869 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865771 | TGAGCTGAGGTCAAA[C/T]CTCGAACAGCAGCAG | 83860 |
rs772982390 | in-del | -/ATAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867769 | GTTGACCCTTGAACA[-/ATAT]GGGAGTTGGGGGCAC | 83860 |
rs772988845 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016775 | CCCCCCAATCTTACT[A/G]TCTGAGAGACTTCAG | 83860 |
rs773000679 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009973 | CTGGAGTGCAGTGGT[A/G]CGATCTCGGCTCACT | 83860 |
rs773001299 | in-del | -/AAAAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898546 | ACAAGACTCTGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAT | 83860 |
rs773053146 | snp | C/T | 1.65671e-05 | 0.00287807 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824532 | ATACATTCCTGATTA[C/T]CTGCCACCCATTGTG | 83860 |
rs773077912 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923404 | AAATGGACTCGTGTC[C/T]TTTGGGGTGGGGTGG | 83860 |
rs773081161 | snp | C/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7816557 | CCCAGGTAGCCCTCA[C/T]GCAGTGACCTGTTCC | 83860 |
rs773086771 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892059 | AATTTCAAAACCCAG[A/G]TGTTTAATTATTCAT | 83860 |
rs773109091 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975381 | ACACTTATCTTAAGA[C/G]TTACTAGGGTCAGAT | 83860 |
rs773116566 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919520 | ATGATAATATGCATA[C/T]AGAGCACCAGTGGGA | 83860 |
rs773122986 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877009 | TACTCAAATTGCCCA[C/G]TTTCCTATCTGCTCA | 83860 |
rs773128289 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012340 | GGAAATGCCACTTAA[A/G]TTCCCTTAGCTCCGG | 83860 |
rs773141027 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948311 | CCAGGCTGGTCTTGA[A/G]CTCCCAGCTTCAAGC | 83860 |
rs773174483 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962416 | AACACATACCCCACA[C/T]GTTTTTCTCTGTTGT | 83860 |
rs773178479 | snp | C/G | 3.32618e-05 | 0.00407797 | missense | TAF3 | GRCh38.p7 | 10:7964916 | GGACAATGGATGCCT[C/G]CATTGATGAGGTTGT | 83860 |
rs773198666 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996710 | GGATTTTTTTTGAGA[C/T]AGGGTCTCAGCCAGA | 83860 |
rs773228009 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963510 | GAAGATCCTTGAAAA[C/G]TAACTTACTTTTTAA | 83860 |
rs773243864 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980637 | TTACAGTCTCAACAC[C/G]TAGAGACAACATATC | 83860 |
rs773252150 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907179 | TCCTGGAGTTGAAAG[C/T]AGGGGCACAGTCACA | 83860 |
rs773258886 | in-del | -/GG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935627 | CTAAAGCTAAGTAGA[-/GG]GCCAGAGAATACTGG | 83860 |
rs773266356 | snp | C/G | 1.73893e-05 | 0.00294862 | missense | TAF3 | GRCh38.p7 | 10:7964510 | CACATTCCCCAAACA[C/G]CTGTGAGACCTGAAA | 83860 |
rs773274059 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825502 | CCCCATTCTCCACCA[C/T]TTCCAGCCCCTGGCA | 83860 |
rs773278983 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877951 | TTGGAGCTAATGTTT[C/T]TGTCACCTTACCTGT | 83860 |
rs773280673 | snp | C/T | 1.66785e-05 | 0.00288773 | missense | TAF3 | GRCh38.p7 | 10:7964595 | TCCAGGTAAAACAAA[C/T]ACAGACACCCCCTGA | 83860 |
rs773298146 | in-del | -/TTTA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875226 | TGTCTCCATACATTG[-/TTTA]TTTATTTAACCATTT | 83860 |
rs773315855 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851268 | AGCCAGGCAGGCCAT[C/G]TGGGGAGTGAGCACT | 83860 |
rs773327680 | snp | C/T | 1.67069e-05 | 0.00289019 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7977261 | AGTGGAACCAGTCGC[C/T]CTGGCCCCGAGTCCA | 83860 |
rs773343263 | snp | A/G | 0.000137979 | 0.00830483 | intron-variant | TAF3 | GRCh38.p7 | 10:7975135 | AGAAAGACTGAAGAT[A/G]CTGTAAATAAGCAGA | 83860 |
rs773363497 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879832 | AATTAAATAAAATAC[A/C]TATTTGGATTTTTAA | 83860 |
rs773367979 | in-del | -/CACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006197 | ACACACACACACACA[-/CACACAC]ACACACACACACACA | 83860 |
rs773391201 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911070 | ATGGTATTTTGACTT[C/T]AATTATATGATTTTT | 83860 |
rs773409257 | in-del | -/TTTTGACT | 1.79338e-05 | 0.00299443 | intron-variant | TAF3 | GRCh38.p7 | 10:8009044 | TCGATGATGATCCTG[-/TTTTGACT]TTTACCTTCTCTTCT | 83860 |
rs773413388 | in-del | -/CAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959157 | ACACACACACACACA[-/CAC]ACACAAAAAAAGTTT | 83860 |
rs773457903 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825872 | TGTACCTTGAAGTAG[-/A]ATTGCTGGATCATAT | 83860 |
rs773492531 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898415 | GCTGGGCATGATGGC[A/G]GGTGCCTGTAATCCC | 83860 |
rs773504633 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872975 | ATTCATGAAGTTATA[A/C]TTTATCCATAAATCC | 83860 |
rs773505375 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912014 | GATCATCCAGAATTC[G/T]GAAATCATAATGATT | 83860 |
rs773515140 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903830 | ATATTGAAATGACTG[A/G]GATATAGATCCTCCC | 83860 |
rs773523603 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7934369 | GACATCTTAGATTCA[A/G]TGAAATGTGGTAGGC | 83860 |
rs773524697 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868792 | GTAATACATTTAATA[C/T]AATAATTATGATTTT | 83860 |
rs773559523 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880832 | GTGCAACAGATGTAT[A/G]TTTAAACGATATACC | 83860 |
rs773576088 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867849 | CTTTACTAATAGCTT[A/G]CTGTTGACTGTAAGC | 83860 |
rs773579209 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7824304 | AATTTGATTTGCTTT[G/T]CACTTTGTTTCAGAT | 83860 |
rs773619119 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007531 | GATTATTACCTAACT[C/G]TCTGTTATATTGTTT | 83860 |
rs773632806 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916376 | CCTGCTGTAACTCAT[C/T]AGCGTCACATGTAGA | 83860 |
rs773637098 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986321 | TTCTGCCTGGGTGAA[A/C]CAGCAGCACCTCAAA | 83860 |
rs773639128 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001456 | GAATAAGAACATTAA[C/T]TCTTTTTTATTCACA | 83860 |
rs773649453 | snp | C/T | 3.3123e-05 | 0.00406945 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8013787 | GTGTAACAAGCCTGA[C/T]GATGGGAGTCCCATG | 83860 |
rs773700577 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958112 | CTTTGTTGCCATTCA[A/G]TTATTATGAAACTGA | 83860 |
rs773702826 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943171 | CTGAGAACTCCACTC[A/G]GCCTCCAGCGCTGCC | 83860 |
rs773729447 | snp | C/T | 6.64022e-05 | 0.00576166 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964242 | GGCACCTCCCTCACC[C/T]GAGCCGCCAATGTTG | 83860 |
rs773729626 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928198 | TAAATACTACTCTTA[A/C]TGTTTTGTATATTCC | 83860 |
rs773739558 | snp | C/T | 1.68298e-05 | 0.00290079 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965286 | CTACAAGTTTAAAAT[C/T]AAAGAATTTGAAGAT | 83860 |
rs773741222 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7831295 | GACTAGTTTCATTTA[A/G]TACTCTATCATTGTG | 83860 |
rs773746346 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904616 | AAGATTTGCTGATAC[A/G]TAGATAGTAGTGAAG | 83860 |
rs773753481 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945792 | TGTCCTGTCTAAAGT[C/T]GCCCTTTTTCTCTCC | 83860 |
rs773760140 | snp | A/G | 0.000107888 | 0.00734388 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009117 | CCCCGAGGCCAAGCC[A/G]GCGCCCTCGCAGAAC | 83860 |
rs773760600 | in-del | -/CT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832236 | GTAACCACTGTTCTA[-/CT]CTCTGCTTCTTGGAA | 83860 |
rs773767461 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979073 | AAGGCAGCCAGATGC[A/G]GTGGCTCACGCCTGT | 83860 |
rs773777072 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922938 | AAACTTGTATCTTCC[A/T]GATTCTACACTTAAA | 83860 |
rs773797662 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892118 | TATTTACAACTTTAT[A/G]CATTACAAAATTCAG | 83860 |
rs773797920 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884542 | TAGGCGCCCGCCACC[A/G]TGCCTGGCTAATTTT | 83860 |
rs773810872 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946598 | CGTAGTAGCACATGT[A/C]CTTGGTCCCAGCTAC | 83860 |
rs773816677 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970954 | ATGAAGGGTTTTTTT[G/T]GTAAATAAACCCAAT | 83860 |
rs773821683 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960002 | TGGAGAACACACACT[C/G]TTAGAGCTGAGCTAT | 83860 |
rs773869694 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971954 | TGTATTTTTAGTTAC[C/T]TACAAAGGAGTCTTA | 83860 |
rs773902106 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844697 | TCTTCTTTTTAGTCT[A/C]TGCCTGTCTTTTTCC | 83860 |
rs773913901 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906305 | ACAAACAAGATATCT[C/G]ATAACGCCCACATTT | 83860 |
rs773920670 | snp | A/C | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014996 | GGCCTGGGGGCTGCC[A/C]CTCCTCCACTTCTCT | 83860 |
rs773945058 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7958535 | TTTATGTAAAGTTCA[A/G]AAACAAGCAAACTAC | 83860 |
rs773953738 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916545 | ACTAACATCATGTTT[A/C]ACACATAATTTTCTT | 83860 |
rs773956528 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870258 | GAGCATGAAATTCTC[A/G]TCAGTCATTGGTTGT | 83860 |
rs773959131 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929512 | AAGTGATCTTCCTGT[C/G]TCAGCCTCCAGGTTA | 83860 |
rs773966776 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010962 | AGTCCACATTGTTCT[A/G]GGACTGTTTTTTAGT | 83860 |
rs773975254 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989452 | TGCTGAGAAACATCT[A/G]TTTGCATTATTTATT | 83860 |
rs774006876 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8005013 | CTTGTTTCCAATCTG[C/T]TGTTAAATCCCTCCT | 83860 |
rs774030003 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867254 | ACAGAGTGAGACTGT[-/CA]CACACACACACACAC | 83860 |
rs774059395 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892732 | GTTGGTCAGTTAGTC[-/T]TATCTATCCATCTTT | 83860 |
rs774074166 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922989 | CTCTTAATGTATTAT[-/A]AATCATCTATATAGG | 83860 |
rs774095751 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939433 | GTAGCCCGCCAGTTA[A/G]CAAAGTCCCAAACAT | 83860 |
rs774101421 | snp | C/G | 1.65787e-05 | 0.00287907 | missense | TAF3 | GRCh38.p7 | 10:7964144 | GTTGTGTTATTGGAA[C/G]CTCGAGAGCCACTCA | 83860 |
rs774102738 | in-del | -/TTTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860784 | AACAGGAGCCTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 83860 |
rs774122935 | in-del | -/TGG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931502 | CCCATCATTTAAGTC[-/TGG]TGGTAGACCACAGGG | 83860 |
rs774128358 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909424 | TCAGAACAGCACTTC[C/T]GCCAAATTAAAGACT | 83860 |
rs774135436 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887447 | CTTTATCCTTACCAT[C/T]GAGAGACTCCGGATG | 83860 |
rs774146794 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894502 | GACCTGATCGATTCC[C/T]AGATGGTGACTGGAC | 83860 |
rs774154293 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860379 | TAGGAGCATATGATC[-/T]TATGAGAGAATAAAG | 83860 |
rs774197689 | snp | A/G | 1.66302e-05 | 0.00288355 | missense | TAF3 | GRCh38.p7 | 10:7964765 | GAATCTGAAGGAGAC[A/G]TTTTTACTAGCCCTA | 83860 |
rs774199935 | snp | A/G | | | downstream-variant-500B | TAF3 | GRCh38.p7 | 10:8016978 | CACCTCTAGGTCAGT[A/G]AGTCGGATCCAGTCC | 83860 |
rs774210944 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006028 | GCTTGCCTCATGTGG[C/T]CATTATGAAAAACAA | 83860 |
rs774225366 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855607 | ATCCGATTCCTCTAC[A/G]GTGGAGTCCCCACTT | 83860 |
rs774238827 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882616 | TATACTTGGACTCAA[C/T]ATAAGGAAGAATTCT | 83860 |
rs774239027 | snp | C/T | | | upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818370 | CCTCCTCCACCTGCG[C/T]GCCCCACGCCCGCTT | 83860 |
rs774254764 | in-del | -/TGTTTTTTTTTTTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842163 | ATTGTTTTTTTTTTT[-/TGTTTTTTTTTTTG]TTTTTTTTTTTTTTT | 83860 |
rs774254815 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985780 | CTCATTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 83860 |
rs774260316 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908672 | GCCACCAGAGCCACA[A/C]AGCACATAATGAGGC | 83860 |
rs774274813 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7948783 | TACTGAACTAATGTT[A/T]ATCTTACCAGTTCAA | 83860 |
rs774277252 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828284 | AAGTAGTGTTACCAT[C/T]ACGTGCTGAGGATCT | 83860 |
rs774277838 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866945 | AATTTAAATTCCAAA[C/G]TGAGGAAAGCAGTTT | 83860 |
rs774293127 | snp | C/G | 1.65611e-05 | 0.00287755 | missense | TAF3 | GRCh38.p7 | 10:7824380 | CTGATGGGGGTTAGT[C/G]TACATGAACTAGAAG | 83860 |
rs774297718 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7988109 | AATGTTTATAAGTAA[A/C]CAATTTTTAAAAACA | 83860 |
rs774315900 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950895 | GAAGTCCTGTCTAGT[A/G]GTCCCAGTGCCAGAG | 83860 |
rs774319780 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849638 | CCCAATTATCATATA[C/T]TAAAATTATAACAAC | 83860 |
rs774321933 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836399 | CCTGTCTCAGCCTCC[C/T]GAGTACCTGGGATTA | 83860 |
rs774326853 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985078 | TCTTCGCTTTTCCCA[C/T]GCCTGCCTGCATAGC | 83860 |
rs774327068 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820857 | TTATCTTGAAAGTAC[A/G]TCACCAGCTGACTAC | 83860 |
rs774359799 | snp | A/G | 1.7886e-05 | 0.00299044 | missense | TAF3 | GRCh38.p7 | 10:7965645 | AGAAGAAGAAAAAGA[A/G]GGAAAAAGAGAAGGA | 83860 |
rs774382875 | snp | C/G | 2.03523e-05 | 0.00318994 | missense | TAF3 | GRCh38.p7 | 10:8009176 | CGCCCGCCCCCGGCC[C/G]CATGCTCGTCAGCCC | 83860 |
rs774390193 | in-del | -/CA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959141 | CGAGATTCTGTCTCA[-/CA]CACACACACACACAC | 83860 |
rs774406770 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935629 | AAAGCTAAGTAGAGG[C/G]CCAGAGAATACTGGG | 83860 |
rs774417691 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858425 | TACAATCGTTTATGT[C/G]AGCTAGGCTACAATT | 83860 |
rs774422506 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856197 | AGCAGAATCAGAAAA[G/T]ATTTTGGCTGGGCGC | 83860 |
rs774447724 | snp | C/T | 3.34102e-05 | 0.00408705 | missense | TAF3 | GRCh38.p7 | 10:7964421 | TTCGATCACCAAAAA[C/T]TGTATCCAAAGAAAA | 83860 |
rs774447869 | snp | A/G | 1.91437e-05 | 0.00309378 | intron-variant | TAF3 | GRCh38.p7 | 10:7965769 | CTCATTTTTGGCCCT[A/G]TCTGAACAGAGTCCT | 83860 |
rs774452819 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896674 | TAGGAAAAGAGGAAC[A/C]TATATAATAGCAAAA | 83860 |
rs774490495 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002518 | ATAGAAATTAGAAAG[C/G]CTTTTTGTTCCTTTG | 83860 |
rs774505614 | snp | A/G/T | 0.000128369 | 0.00801066 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014753 | ATCGAGCCCACTGAC[A/G/T]ACTCCCGAGGGGCTG | 83860 |
rs774508645 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943051 | TTTCTGTGTCTGTGT[A/T]TGTTTACTCCCGAAA | 83860 |
rs774510996 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838165 | AGCTGGATTAGGGTT[C/T]AGTTGACTCCGTTCA | 83860 |
rs774511812 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853884 | GCAACCACAGGTTGG[-/C]CCACTGATAGATAAG | 83860 |
rs774544704 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998509 | TTTTAAGCCATTCTA[A/T]TGGGCGCCATTATCA | 83860 |
rs774580178 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888545 | AGTGTGGAGGGTTGA[C/G]AGGGCTCATTCACTC | 83860 |
rs774625139 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829820 | GAATGGGAGTTATGC[A/G]TCCCGCTTTGAAGGT | 83860 |
rs774628688 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869213 | AAGATGTCACATATA[A/C]TCCCATGAAGAATAA | 83860 |
rs774637720 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931824 | AGATATACAAATGAC[A/T]GACAGTTCCTACCTG | 83860 |
rs774645013 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975273 | CCTCACCGGTATTTC[C/T]TGTGGAGTTAGATGT | 83860 |
rs774648600 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892307 | GGGGGCTAGAAAGCA[C/T]GCTCAGTGTGGGTGA | 83860 |
rs774665170 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824520 | GGAAAGAAAAGAATA[C/T]ATTCCTGATTACCTG | 83860 |
rs774692257 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7851713 | AATGTTTTAAGCATA[C/T]AACTCTAAAAGATAA | 83860 |
rs774692800 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989179 | GAGATCACGTGACCA[A/G]CCTGAACCAATCACT | 83860 |
rs774718478 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7858441 | AGCTAGGCTACAATT[A/G]TGATCATTAGCAGGG | 83860 |
rs774722539 | in-del | -/AAG | 3.37935e-05 | 0.00411043 | cds-indel | TAF3 | GRCh38.p7 | 10:7965074 | TCCTCCGTGGAGGTA[-/AAG]AAGAAGTTGAAAAAG | 83860 |
rs774750729 | in-del | -/TTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7986383 | TTTCCGCCAGTGTGG[-/TTC]TTCTTCTTTTTCGTA | 83860 |
rs774754086 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983183 | GTGCTCACAGTCCCT[A/G]GCGAAGCCCCGCTTC | 83860 |
rs774765735 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905677 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 83860 |
rs774771553 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974085 | GTGAGCCAAGAACGT[G/T]CCACTGATCTCCAGC | 83860 |
rs774774628 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864511 | CGTAGTCACATTGCT[A/G]TACAACAGATCTCTT | 83860 |
rs774778335 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839030 | GCCTGTGGTGTTCAG[C/T]ACACGTGTCTTAGCA | 83860 |
rs774790162 | snp | A/C/G/T | 0.000105783 | 0.00727206 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009315 | CGTGGTGACTGAGAC[A/C/G/T]GTCAGCACCTACGTG | 83860 |
rs774796814 | in-del | -/TACACACA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006179 | TACTGAAAAAAAAAA[-/TACACACA]CACACACACACACAC | 83860 |
rs774807233 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980705 | AAGCCTTGCCTTGAT[G/T]CTGGGATAGCAAGTA | 83860 |
rs774822728 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822063 | AGACAAAAGAATTAA[A/C]ACATGTAGTAGAAAA | 83860 |
rs774834780 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993302 | TCCCACCTCAGCCTC[A/C]CAAGTAGCTGCAACT | 83860 |
rs774852729 | snp | C/T | 3.37775e-05 | 0.00410945 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965247 | TCCCTGGAAGGAATT[C/T]CTTAAAGAGGAAGAG | 83860 |
rs774864836 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852649 | GTGTAACTCCGTCAG[A/T]GTACACATAATATCA | 83860 |
rs774867377 | snp | A/G | 3.31603e-05 | 0.00407174 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964134 | CACGCTAGATGTTGT[A/G]TTATTGGAAGCTCGA | 83860 |
rs774874385 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013265 | GTAATAAGGTGGTGC[A/G]TGCACATTTGGCTGT | 83860 |
rs774875869 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821120 | GGTCACTGCAGCTCT[G/T]CAGTGTAAACCTTGT | 83860 |
rs774882108 | snp | C/T | 1.90282e-05 | 0.00308444 | intron-variant | TAF3 | GRCh38.p7 | 10:8009366 | CGGTTAGCATGGAGA[C/T]GTTTTCAGATCGAGA | 83860 |
rs774906583 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935742 | CTACAGGTCCACTGG[A/G]GAAGCACATTCCAAA | 83860 |
rs774949276 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936857 | TCCCTCCCTGTACCC[A/G]CTGGCATCCATTGAT | 83860 |
rs774954692 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881345 | CTTCAGTTATATTTC[A/G]ATATCCTAGGTTCCT | 83860 |
rs774956205 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7960147 | ATGAACCTCTGTGGA[A/G]TAGGAGGAGGTTCTT | 83860 |
rs775002563 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925034 | TATATAAATAATTTT[A/T]TAATTCACTTTTTCA | 83860 |
rs775011480 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864670 | TCTTTTTATTATTCA[C/G]CTGTGAAAGTTCTTT | 83860 |
rs775036372 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973760 | ACACAGAAAGATGAG[A/G]AAGTCTTAAATAGTT | 83860 |
rs775042662 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834257 | CGCTTTTGGGGCCAA[A/G]TATAAAAAATAATTG | 83860 |
rs775054550 | snp | A/G | 1.66735e-05 | 0.00288729 | missense | TAF3 | GRCh38.p7 | 10:7964009 | GATGAATTGGAGGAG[A/G]AAGAAATTATTAATG | 83860 |
rs775062189 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947980 | CTATGTTGACGCACT[A/G]TAACTTCCTGACATA | 83860 |
rs775082057 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874813 | AAAACTTTTTTCATC[A/G]ATTTCTTAGCTGTAT | 83860 |
rs775118575 | in-del | -/ATG | | | cds-indel | TAF3 | GRCh38.p7 | 10:8015704 | GCAGTGCCCGGAAAC[-/ATG]GTGGGGAAAGGGCCC | 83860 |
rs775141573 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993452 | CCGAATTGCTGAGAT[G/T]ATAGGCGTGAGCCAC | 83860 |
rs775181194 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906068 | TAAAAGTGCTCGTGG[A/T]TAACACTTGATGCTA | 83860 |
rs775201781 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887096 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGCACCT | 83860 |
rs775235643 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864570 | TAATGTGTCCTTCAT[C/G]TACAGGTTTCTGTGT | 83860 |
rs775248926 | snp | C/T | 1.68261e-05 | 0.00290048 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965053 | GAGGAGAAAACCAAG[C/T]TGCCTTCCTCCGTGG | 83860 |
rs775279950 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822160 | GTGATGTGCATAAGA[C/G]ATTGAAGTGGGCAGA | 83860 |
rs775289051 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863951 | TTTAAGAACAGTTTT[A/G]GATTCATAGCAAAAT | 83860 |
rs775300709 | snp | A/G | 1.79722e-05 | 0.00299763 | missense | TAF3 | GRCh38.p7 | 10:8009113 | CTGCCCCCGAGGCCA[A/G]GCCGGCGCCCTCGCA | 83860 |
rs775308907 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985221 | CCCCAGCTGATTAGA[C/T]TTGCCTTTTGGGTTC | 83860 |
rs775341310 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952346 | AAGAAGAGTGATTAA[C/T]GATAGCAATTTATTG | 83860 |
rs775348986 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7844933 | TTTTAAAATATTGCA[A/G]TGTTGCATCAAATAT | 83860 |
rs775352469 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7995067 | AAGAATTATATAAAA[G/T]AGCCTAAAAGTAATA | 83860 |
rs775377253 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999854 | CTGCTATGGATGATG[C/T]ACTCAACTTAGACGC | 83860 |
rs775379065 | in-del | -/AAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975071 | ACAAGACTCTGTCTC[-/AAAAAAAAA]AAAAAAAAAAAAAGA | 83860 |
rs775403792 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826518 | ATAGATTTTTGGGTT[A/T]CTTTTCTGGGTTATT | 83860 |
rs775407339 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989307 | AGAAGGAAGAGAGAG[A/G]GGGCTGAAGGCAGGG | 83860 |
rs775415341 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956348 | AAAAGTTAGCCAGAC[A/G]TAGTGGCACGTGCCT | 83860 |
rs775415746 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927738 | TGATAATATATGTAG[C/T]TGATAATACAATAGG | 83860 |
rs775444779 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833906 | CTTCAGCCGCTGCAC[A/G]GTGCGTGTGGAAGTG | 83860 |
rs775456901 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825920 | TTTTTGAGGAAGCAC[C/T]ACACTGTTTTCCACA | 83860 |
rs775460238 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975436 | CAGTAAGCAAAACGC[A/G]CATGGTCCCTGCCCT | 83860 |
rs775467612 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972126 | TTTTGGCTTGATGCC[A/T]TTAAAAGATGGCATT | 83860 |
rs775481987 | snp | A/G | 2.71639e-05 | 0.00368527 | intron-variant | TAF3 | GRCh38.p7 | 10:8014586 | ACATGGAAGGGAGAA[A/G]AATAGATGTCTGTAT | 83860 |
rs775496376 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894787 | CTTTATTTAAATACA[A/G]GATGGATGGTGTTTT | 83860 |
rs775501119 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000654 | CATGGTGGCACGCAC[A/C]TGTAGTCCCAGCTAC | 83860 |
rs775516262 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941805 | ACTCGTGGGTGCTTG[A/G]TCTTAGAGAGCCTGG | 83860 |
rs775516627 | snp | C/G | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7818135 | CACAGATTTTTAGCT[C/G]AGGCAACACCAGCGC | 83860 |
rs775517933 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929702 | TTGCTTATCTGTATA[A/C]AATATAATAAGGTTA | 83860 |
rs775532929 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943159 | CTCCGTGAGACTCTG[A/G]GAACTCCACTCGGCC | 83860 |
rs775550350 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838485 | CTCCCGGGTTTGAGC[A/G]ATTCTCCTGCCTTAG | 83860 |
rs775554483 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889673 | CCTCTTAGTTATTCT[C/T]CCCAAGAAGGAATTA | 83860 |
rs775569991 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829884 | GCATGGGGATTTCTC[C/T]CTTTCCCCACTAAGA | 83860 |
rs775571723 | snp | C/T | 1.65433e-05 | 0.002876 | missense | TAF3 | GRCh38.p7 | 10:8014722 | AAGAAGGACAAAAAG[C/T]ACAAGAAGAGGAAGC | 83860 |
rs775585989 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896254 | TTCTTTTTCTCAGAT[C/T]TTTACTCTTGTGACT | 83860 |
rs775586269 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944564 | GTCTGAGATAGAGCA[A/G]GAGTGAGCCTCAGAA | 83860 |
rs775594635 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985383 | TTAGCTCCTCTCCTC[-/TG]TGTCTTCCTCTTCTT | 83860 |
rs775608916 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002603 | TTTTTTAGCCTTAAG[A/C]AATTGGGTCAGTTTC | 83860 |
rs775625805 | snp | A/G | 3.28057e-05 | 0.00404991 | missense, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818828 | CGGACGTGCTGCAGC[A/G]CTATCTGCAGCAGCT | 83860 |
rs775636719 | snp | A/C | 1.67024e-05 | 0.0028898 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7977298 | CCCAGATTAACTCTC[A/C]GAGTCGGTGCTGGCC | 83860 |
rs775639287 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933325 | GAAAGAGTTAGATCA[C/T]ATCTTGCTCACTCTG | 83860 |
rs775662435 | snp | A/C | 1.6664e-05 | 0.00288647 | missense | TAF3 | GRCh38.p7 | 10:7965486 | TGGTGTTGCCCCCAA[A/C]AGAGTTGGCCCTGCC | 83860 |
rs775690736 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859752 | CTAGAATGTAATCCA[C/T]GAGAAGAGATATTTT | 83860 |
rs775699589 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966782 | CTTACCTAGAAAACT[G/T]AGTGTATTTGACAGC | 83860 |
rs775710076 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824340 | AACAGACCCAATTTT[A/G]GATGATGTTGGTGAA | 83860 |
rs775716503 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7836116 | TTGGTGCTTCTAAAA[-/T]TTTATCCTTCACCTA | 83860 |
rs775740366 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823046 | TGAGCCTGGGAAGGT[A/G]AGGTTGCAGTGAGCC | 83860 |
rs775758669 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852804 | AGAGAAACTTCCTAT[C/T]ATCTACTATTTGGTT | 83860 |
rs775787041 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920468 | GCATTTTGTTCTGCA[A/G]TTTAAATGATAAAAA | 83860 |
rs775790585 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013484 | GCTTTTTATGACTTA[C/G]AAAAGAAAGCTTAGA | 83860 |
rs775791400 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969307 | CTTAAAAAAAAAAGA[C/T]ATGTTAAGAGCACTT | 83860 |
rs775792138 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962508 | TCAAAAGTCCTAGGA[G/T]CTGGATGCAATTTTA | 83860 |
rs775802070 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848229 | GTAAAAAATATTTCT[C/T]AGATTTAATGGCATT | 83860 |
rs775835028 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861242 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCATC | 83860 |
rs775841075 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841490 | ACATCAGAGGTCTCT[-/A]ACCTAGTGTGCTTAC | 83860 |
rs775843927 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014900 | GCTGGAACACACCGC[A/G]CACCTGGATTGTTCA | 83860 |
rs775845764 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001584 | CATATAAAATTGTCG[C/T]GCAGTCAAATCAGCA | 83860 |
rs775866526 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880490 | ACAGTGTGCCACAGT[A/G]TTGAAGAGAAGTGAG | 83860 |
rs775873315 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994996 | AAAAAAAAAAAAAAA[-/G]AAAAAAGAAATCCTG | 83860 |
rs775893771 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962324 | CACTTCAGTAATCCA[C/T]GTTATTGCTCTCCTT | 83860 |
rs775901959 | snp | A/G | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965613 | GAAGGAGAAAGAAAA[A/G]AAAAAGGACAAAAAG | 83860 |
rs775904530 | snp | A/C | 1.66059e-05 | 0.00288144 | missense | TAF3 | GRCh38.p7 | 10:7964810 | CCGGAGTGTACTACT[A/C]CCAAAGCTTCCACTT | 83860 |
rs775924873 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840281 | CCTCAGCCTCCTGAA[A/T]AGCTCTGACTACAGG | 83860 |
rs775928175 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903311 | CCCCTACAGGTGACC[C/T]CTGTGTCCTTTGACA | 83860 |
rs775948779 | snp | C/G | 1.91082e-05 | 0.00309091 | intron-variant | TAF3 | GRCh38.p7 | 10:8009358 | CGCCCGCGCGGTTAG[C/G]ATGGAGACGTTTTCA | 83860 |
rs775962225 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882697 | AGTAAGATCACTCCC[G/T]CAATGAGCAAGCTTT | 83860 |
rs775995643 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955548 | AGTTGCATGCGTCTG[C/T]GTAGTTAGTCAGATA | 83860 |
rs775999393 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841563 | GGATGATTTCATTAT[A/T]AATTCTGTTGGTACT | 83860 |
rs776014109 | in-del | -/CC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873618 | AGACATCCGAGTTCT[-/CC]CCCCCCCCCCGTCAA | 83860 |
rs776015292 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7884208 | GTTATTATTTATTTC[A/G]CTGCTTCAGCTGTAC | 83860 |
rs776022138 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926263 | TATTTTAATATATCA[A/C]ACTTTTTTTTTATTA | 83860 |
rs776026152 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870428 | TTGTTTCTTTTCTTC[C/T]AGTGGTCGGTTAGAA | 83860 |
rs776030663 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846104 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCT | 83860 |
rs776064449 | snp | C/T | 1.66529e-05 | 0.00288551 | missense | TAF3 | GRCh38.p7 | 10:7964928 | CCTCCATTGATGAGG[C/T]TGTACGTAAAGCAAA | 83860 |
rs776124817 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908286 | TTTCTGCCTGAAGGC[A/C]ATGGCTACTGCTTAG | 83860 |
rs776152577 | snp | A/G | 1.67897e-05 | 0.00289733 | missense | TAF3 | GRCh38.p7 | 10:7965038 | CTCCACAAGGTGTAT[A/G]AGGAGAAAACCAAGC | 83860 |
rs776154176 | snp | C/T | 1.66228e-05 | 0.0028829 | intron-variant | TAF3 | GRCh38.p7 | 10:7824572 | GAAGGTTTGTGAGTG[C/T]TTCTTCTTCATATGT | 83860 |
rs776188356 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922948 | CTTCCAGATTCTACA[C/T]TTAAACCGCTTAATA | 83860 |
rs776196557 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015117 | GATGAGAAGATAATG[A/T]ACAAACTGCCTCAAC | 83860 |
rs776212328 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982484 | GCTCACTGCAACCTC[C/T]ACCTCCCGGGTTCAA | 83860 |
rs776321435 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903623 | ATTGCTTAGCTGATG[A/C]AGTTTAGCATTGCAC | 83860 |
rs776321741 | in-del | -/A | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8015856 | AGTTTCCATGAAAGT[-/A]AAAAAAAAAAAACAA | 83860 |
rs776323269 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973892 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGCAGA | 83860 |
rs776324568 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894952 | ATGGTCTTGGCTCAC[C/T]ACAACCTTTGCCTCC | 83860 |
rs776365464 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961411 | ATGCTTTTGCAGCAT[A/G]GCTTCTGCTGTTGGC | 83860 |
rs776371872 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854336 | CCCCAAACTGCCTAC[A/G]TAAGATAACTGGAAG | 83860 |
rs776417340 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887583 | AACATAAGACTTTCC[C/T]AGTGATAAGTGTGAA | 83860 |
rs776466612 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7972808 | TTTGGTTGAGTGAAG[G/T]TGGGGCCAAGGTTAA | 83860 |
rs776483566 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942025 | TTTGTTTTGAGGTCA[A/G]TTTTTTTGCTTCACA | 83860 |
rs776488547 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7944010 | CTGCAATTGATATGC[A/G]TAAGAGGAAGAATGC | 83860 |
rs776490332 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968385 | CTTATAAAGCTGATA[C/T]CAAGAACCAATAAAG | 83860 |
rs776492763 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834397 | GTATGAGATAAGGAT[C/G]CAATTTCATTCTTCT | 83860 |
rs776504046 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7828046 | TTGAATTGAAATACA[A/G]TATACATTAGTGAAG | 83860 |
rs776529811 | in-del | -/TGTGTGTGTGTGTGTGTGTGTAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920311 | ATACGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTGTGTAT]GTGTGTGTGTGTGTG | 83860 |
rs776534008 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888222 | TTTTACAACCAAGCC[G/T]CCTAAAACACTGTCC | 83860 |
rs776538255 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8006575 | TCTTGATCTTTGGCT[C/G]TATCCAAGTTAGGAA | 83860 |
rs776551072 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951296 | CTAGCTTACAATTCC[A/G]TGAGTTTGCATTTTG | 83860 |
rs776561356 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849865 | GTGTATTTTTTGTAG[A/C]TACCAGGTTTTCACC | 83860 |
rs776567262 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945674 | GGGTGTGCCCTTGCT[C/T]CTCTGCCCCTGAAAT | 83860 |
rs776593902 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7963743 | CAGCAAATTAACAGG[G/T]CACATGTATACCTGT | 83860 |
rs776618132 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7862159 | TCTCCTGAGATTGCC[A/C]GTGAATATATTTTCC | 83860 |
rs776621317 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7930930 | AAGGATCTTTATAAG[G/T]CCCACAAGTTTGTCT | 83860 |
rs776631526 | in-del | -/AGA | 0.00248136 | 0.0351358 | splice-acceptor-variant, intron-variant | TAF3 | GRCh38.p7 | 10:7963918 | TTTTCTTCCTTTACC[-/AGA]AGAAGAAGAAGAGCA | 83860 |
rs776647063 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951117 | TATAGGAACCTAACC[G/T]TGTATTTCTCTTAAG | 83860 |
rs776651322 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997906 | TTTTTACAACGATCA[A/G]TTTAGATTAAGTGAT | 83860 |
rs776666478 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918405 | TAGAGTAAGGGAAGA[A/G]TGGGATTTGACCAGG | 83860 |
rs776677860 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866984 | ATGATTTCGGCTGGG[C/T]GTGGTGGCTCACACC | 83860 |
rs776702223 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878469 | GGTGACGGGAGGAGT[A/G]AGGGTACAGGTGATG | 83860 |
rs776720944 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919285 | AGTTTTCTGCAGGCC[C/T]CATCTGGGGCTTGGT | 83860 |
rs776724341 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978627 | CTTACCTACAGAAGC[A/G]TGAAGAATGTCCTCA | 83860 |
rs776760740 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978728 | ATGGGCTCATTTCTC[C/T]AAGAGGAAGATGTTG | 83860 |
rs776762404 | snp | A/G | 1.66214e-05 | 0.00288278 | missense | TAF3 | GRCh38.p7 | 10:7964700 | ATGCTGTGATTGCAC[A/G]AGCCTGTGCTGAGCG | 83860 |
rs776763633 | snp | C/T | 1.66682e-05 | 0.00288684 | missense | TAF3 | GRCh38.p7 | 10:7964601 | TAAAACAAATACAGA[C/T]ACCCCCTGATGCTGG | 83860 |
rs776764260 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933611 | AAGTAGGACAGTATT[C/G]ACAGTGGTGAAGTGA | 83860 |
rs776780956 | snp | C/T | 7.94145e-05 | 0.00630087 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818805 | GCTCAGCGCCTGCCA[C/T]CTCCTCACGGACGTG | 83860 |
rs776786230 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890998 | ATGTAGCTGAACTTG[C/T]GGATGCCAGTACACA | 83860 |
rs776813561 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7848499 | TACCTGTATATGGAG[C/T]CCATCTCAGCAGGCA | 83860 |
rs776822622 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8002897 | TTTAAACTGTTATAG[C/T]TTCCTGGCAAATTGG | 83860 |
rs776832737 | in-del | -/AAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898548 | AAGACTCTGTCTCAA[-/AAAAAAAAA]AAAAAAAAAAAAAAT | 83860 |
rs776845882 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830254 | ATTTAAACCCTTTCT[C/G]CCAGTTCAAGAAACA | 83860 |
rs776855058 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931164 | GTCAAAATGCATCGA[A/G]TGTTTAATATGTATC | 83860 |
rs776862786 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011116 | GCTGTGACTACCAAC[C/T]CTGCAGACTGTGATG | 83860 |
rs776898866 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841705 | AGGATTTGGAGATAG[A/G]TAAATTGTAGAGGAT | 83860 |
rs776915081 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913216 | CCCTGTGTCTACATA[C/T]AGGCACACAGGGGGC | 83860 |
rs776916214 | snp | C/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016328 | CATATTTTAAAACAT[C/T]ATGTGGTTAGAGAAA | 83860 |
rs776946924 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955403 | TTAACCAATCATAAG[-/A]AGTCTAGCTTTAAAT | 83860 |
rs776975238 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7891853 | AAATGTTGTATCTAC[C/T]GGACTTAGCTTTGTT | 83860 |
rs776987866 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861404 | AGCCACCGCACCCAG[C/T]CAACAGGAGCCTTTT | 83860 |
rs776991123 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7859120 | ACAAAAAATTAGCTG[C/G]GCGTGTGGTGGGCAC | 83860 |
rs776996369 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7989410 | GAATGCTGGAAGCCA[C/T]TGGGTTTACTTATAT | 83860 |
rs777034214 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8012057 | TGACATGTGCCTGTA[A/G]TCTCAACTACTCAGG | 83860 |
rs777034477 | snp | C/G | 1.7957e-05 | 0.00299636 | missense | TAF3 | GRCh38.p7 | 10:8009104 | AGGTGGTCCCTGCCC[C/G]CGAGGCCAAGCCGGC | 83860 |
rs777052689 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7823795 | CTGCGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 83860 |
rs777114613 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927511 | TGTCCTTTCTTCCCT[C/T]CTCCACCAGTATCTC | 83860 |
rs777119549 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838162 | CAAAGCTGGATTAGG[A/G]TTTAGTTGACTCCGT | 83860 |
rs777121905 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8011719 | CAGGAAAGATTTTGT[A/G]CTTAACCTCCTTGAC | 83860 |
rs777122223 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843011 | TGACATGCTTTGCAC[C/T]TGCTAGGGCGTAGTC | 83860 |
rs777131247 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871556 | TCAAGTGATTCTGCT[A/G]CCTCAGCCTCACAAG | 83860 |
rs777133667 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003110 | AGCCTGACAACTGAA[G/T]CACTTAGACCTTTTA | 83860 |
rs777136760 | snp | A/G | 0.000580754 | 0.0170306 | missense | TAF3 | GRCh38.p7 | 10:7964252 | TCACCCGAGCCGCCA[A/G]TGTTGGCTCCAGTTG | 83860 |
rs777140079 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950030 | GAAATCGTTTCTCTC[A/G]TTTTTCTAATAATAG | 83860 |
rs777150808 | in-del | -/TTTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840843 | TATTTCATGTTTTCT[-/TTTC]TTTCTTTCTTTTTTT | 83860 |
rs777161171 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840381 | ATGGTCTCGATCTCC[C/T]GACCTTGTGATCCGC | 83860 |
rs777167104 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956519 | TTAAAATAATTTTAC[A/G]GTCAAATGTTGACCT | 83860 |
rs777173056 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855300 | TGGTGCAGCTGAGCA[A/G]CTGCCTCTACAAAAG | 83860 |
rs777213671 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7923483 | TTTTATTCTTCCAGT[A/G]TGTGCCATATCTTTA | 83860 |
rs777217239 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879018 | CAGGCATAAGTCACC[A/G]CGCCTGGCAAATTCA | 83860 |
rs777220226 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957892 | GTAGAAAGGGCCTGT[C/G]ACCCAAATTTTTTTT | 83860 |
rs777234997 | snp | C/T | 3.35751e-05 | 0.00409712 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965320 | GATCCCAAAGTGAAA[C/T]TGAAAGATGGACTTG | 83860 |
rs777316283 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940729 | GGAGGCTGAGATGGG[A/G]GGATCATTTGAGCCC | 83860 |
rs777340656 | snp | C/G | 3.71395e-05 | 0.0043091 | missense | TAF3 | GRCh38.p7 | 10:7965716 | GAGAAGAGAGAAAAA[C/G]AGAAGGAGAAACACA | 83860 |
rs777348228 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985869 | GCTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCAA | 83860 |
rs777364163 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820579 | AGCTCTCTATAGCCT[C/G]GAACTTCAGGGCTCA | 83860 |
rs777364232 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841394 | CTACTTGGGGAAAGA[A/G]GGGCTGGACTCATGT | 83860 |
rs777368926 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903036 | AACCAGCCTGGACAA[C/T]ATAGTAGGACCCCAT | 83860 |
rs777381826 | in-del | -/AGA | 1.82734e-05 | 0.00302264 | cds-indel | TAF3 | GRCh38.p7 | 10:7965660 | AGGAAAAAGAGAAGG[-/AGA]AGAAGGAGAAGGAAA | 83860 |
rs777396363 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990386 | TTTTTATTGTTTTTG[C/T]CATTTTGTTTATTTA | 83860 |
rs777420938 | snp | C/T | 3.46819e-05 | 0.0041641 | missense | TAF3 | GRCh38.p7 | 10:7964490 | AGAGCCCCAAGGTCA[C/T]GACTCACATTCCCCA | 83860 |
rs777431871 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952835 | TTTTAAAAATACATA[A/C]CCACTTACACATGTT | 83860 |
rs777442866 | snp | C/T | 1.71187e-05 | 0.00292559 | missense | TAF3 | GRCh38.p7 | 10:7964550 | GGACTCCTTCAGCTA[C/T]ACTCAGTGAAAAAAT | 83860 |
rs777460010 | in-del | -/ATACACAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863683 | CACACATATATATAT[-/ATACACAC]ACATATATATATATA | 83860 |
rs777467001 | in-del | -/GCC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949025 | CTGTGCCCGGCTGCT[-/GCC]GCCGCTGCTGACAGC | 83860 |
rs777478088 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966244 | TGTGTTTAGGATTAT[G/T]CCTGTCTACAGAACT | 83860 |
rs777485318 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7941560 | CAATCTGACAAAGGA[A/G]GAAGAGCCACTGCCC | 83860 |
rs777494263 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909268 | CTGAGAGGGCTCTAG[C/T]TGATTCTTGTACATG | 83860 |
rs777499997 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8014250 | TTAGACCTCTTCAGC[A/G]GTTCCTAAAAACTGA | 83860 |
rs777530472 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952230 | ATTAGAGATATTGAC[A/C]TTGTCTGAAGAGATC | 83860 |
rs777531711 | snp | C/T | 3.32347e-05 | 0.00407631 | intron-variant | TAF3 | GRCh38.p7 | 10:8013696 | TTTTTTTCCCATTCC[C/T]TCCATTTTTGCCGCT | 83860 |
rs777537608 | snp | A/G | 1.67778e-05 | 0.00289631 | missense | TAF3 | GRCh38.p7 | 10:7965027 | CTCCCGAACCTCTCC[A/G]CAAGGTGTATGAGGA | 83860 |
rs777537904 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916314 | TGCATAAAGCTGTCT[G/T]ATACAAAAGTAGAAT | 83860 |
rs777547302 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910360 | CTTTTGAAATTATTT[C/T]TACTTTATAAATTTT | 83860 |
rs777551830 | snp | C/G | 1.74842e-05 | 0.00295665 | missense | TAF3 | GRCh38.p7 | 10:7965168 | AGAACAAGGACAAAA[C/G]TAAGGAGAAGGATAA | 83860 |
rs777560052 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830898 | CACAGTTGGATGTTG[C/G]GCATTGTGCACTCAT | 83860 |
rs777560957 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914806 | CTTGTCATTAGTCTT[A/G]CAGGTAGAGTGAAAG | 83860 |
rs777585072 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7935175 | CCAGCTACTCAGGAG[A/G]GTGAGACATGAGAAT | 83860 |
rs777590828 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945443 | TATCTTGTTTACCTG[C/G]ATAGTGAGCATTTTA | 83860 |
rs777606406 | in-del | -/TAATT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873096 | AAAAATTAAAAGTAA[-/TAATT]TAATATGTTTATAAT | 83860 |
rs777624744 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937052 | TGAATAATATTCCGT[G/T]GTCTGAATGTAGCAC | 83860 |
rs777687548 | snp | A/C/T | 3.31566e-05 | 0.00407154 | missense | TAF3 | GRCh38.p7 | 10:7964199 | CACCAATGCTTTCTC[A/C/T]AGTCCATGTACAGGA | 83860 |
rs777692572 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000274 | GGCATGCACCACCAC[A/G]CCCAGCTAATTTTTG | 83860 |
rs777698801 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861753 | GTTTGGCTTTCACCA[A/G]TTTAACTAGGATGTG | 83860 |
rs777725983 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821659 | CTCTGTCGGTGTCAC[A/G]TTATATGTTAAATAT | 83860 |
rs777729411 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976664 | CCTCAGGCCTCCCAA[A/G]GTGCTGAGATTACAG | 83860 |
rs777735770 | snp | C/T | 1.69807e-05 | 0.00291377 | intron-variant | TAF3 | GRCh38.p7 | 10:8009349 | CGTACCTGCCGCCCG[C/T]GCGGTTAGCATGGAG | 83860 |
rs777742594 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7879787 | TTGTTTCTTAGTCTT[G/T]TAGACTTGTATCATT | 83860 |
rs777755485 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904009 | GTCTGAGAAGTTTCA[C/T]GGTGCGTCTGAGTTG | 83860 |
rs777780054 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921840 | ACTTATTTTAAAATG[A/G]TTTTTCTTTTCTAAT | 83860 |
rs777798616 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003987 | AACATATAATGGGTT[C/T]ATTGTCGTTACTTTT | 83860 |
rs777814741 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820308 | GTCTCTTTCCCCTCT[C/T]CAGGAGAAAAATTGA | 83860 |
rs777822638 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914636 | GTTTCTGTATTTGGA[A/C]TTTTACTGTAAATTG | 83860 |
rs777830738 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860907 | TGGGTTCAAGCAATT[A/C]TCTGCTTCAGCCTTC | 83860 |
rs777843161 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906613 | GTGACACTGACAAAG[A/G]CTCCTTATACTTTTT | 83860 |
rs777868811 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864426 | GTCACATAGTTAACT[C/G]TTTGTGGTAAGGGCA | 83860 |
rs777869923 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876237 | GACTGGATTATTGTT[C/T]AGGGTTAATTTTCTG | 83860 |
rs777877855 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994431 | CAGAAATAGGAAATA[C/G]ATGGGTTTGAAAAGA | 83860 |
rs777894514 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987951 | TAAGTGCACTACTCA[G/T]GTGAACATAATACTA | 83860 |
rs777903830 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7853595 | TCACATCATTGACAC[A/G]TGAAATTCTCACATA | 83860 |
rs777924214 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013163 | CTTTACTAAAAATGT[C/G]ATAAAGGGAATGGAA | 83860 |
rs777980977 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839543 | AGAGGTGACAGTGGG[A/G]TCCCAGGTTTCATAG | 83860 |
rs777996306 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7969987 | TAAAAACAGTAGTTT[C/T]ATACCTTCTCGAAGA | 83860 |
rs778007545 | snp | C/T | 0.000248882 | 0.0111525 | missense | TAF3 | GRCh38.p7 | 10:7964085 | AAGAACTGCCAGCCA[C/T]GAAGCGGCCTCGGCT | 83860 |
rs778041714 | in-del | -/CAGAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864516 | CACATTGCTATACAA[-/CAGAT]CAGATCTCTTGAAAT | 83860 |
rs778076278 | snp | C/T | 2.22998e-05 | 0.00333907 | synonymous-codon, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818781 | GGCGCTGGGCTGGGA[C/T]TCGGTGCAGCTCAGC | 83860 |
rs778114342 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904467 | CATTGCATATTCTAC[A/T]CCTAGTAGTCTATTA | 83860 |
rs778131121 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7900576 | GAAAACTCCTGTGCC[C/T]CTATAATGTGGGGCA | 83860 |
rs778138246 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887938 | AATATCAGAATAAGT[C/T]GAGGAACTTTTTTAA | 83860 |
rs778164340 | snp | C/T | 3.39242e-05 | 0.00411837 | intron-variant | TAF3 | GRCh38.p7 | 10:7824271 | ATTTAAAAATATATT[C/T]GTGGGATTTCTTCAA | 83860 |
rs778165372 | snp | A/G | 3.32287e-05 | 0.00407593 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964797 | GAGAATTTCAGGCCC[A/G]GAGTGTACTACTCCC | 83860 |
rs778183827 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7882226 | CATCTTATTGGAGAC[C/G]GTCAAGCATCAATCT | 83860 |
rs778187285 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839692 | TTCTTGAGTACAATT[-/A]TTTTTTTTTTAATTG | 83860 |
rs778193500 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875311 | TTTTTTTAAAGTCCT[A/G]TAAATGACGTTCTTT | 83860 |
rs778199840 | snp | C/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817344 | CTGCAGATCGTCATT[C/T]AGCTGAAGAACCATA | 83860 |
rs778221552 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7917764 | AGAAGAGAGGAAATG[A/C]GGAAAGATGGGAATG | 83860 |
rs778223708 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7911887 | CTTTCTGTAATGGGC[C/T]TAGCTTGCTTTACTC | 83860 |
rs778229114 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7898947 | GATGGCAAGTGGTGC[A/G]TTGAACTTCAGGGTG | 83860 |
rs778232617 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857614 | TATGTTGCTTGCATT[C/G]TTCATCCTGTTTGTG | 83860 |
rs778241026 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959665 | TAAATTCAAAGTAAA[A/C]CAATATATTTTCTAA | 83860 |
rs778246401 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7827636 | GATACAAATATTAGC[A/T]GGGCGTGGTGGCGGG | 83860 |
rs778254360 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000719 | GGGAGGCAGAGGTTG[C/T]AGTGAGCCAAGATTG | 83860 |
rs778279563 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008987 | ATTTCGCTACTGGAA[G/T]AAAAGCTATTTTACG | 83860 |
rs778288304 | in-del | -/GTGATGAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877724 | CAACTGAGACCCATT[-/GTGATGAA]GTGATGAAGTGACTT | 83860 |
rs778293675 | snp | C/G | 1.8232e-05 | 0.00301922 | missense | TAF3 | GRCh38.p7 | 10:8009141 | GCAGAACAGGCCGAA[C/G]ACCCCACCGCCGGCC | 83860 |
rs778310731 | snp | A/G | 1.65844e-05 | 0.00287957 | intron-variant | TAF3 | GRCh38.p7 | 10:8013871 | CTGCCGGCCACACTC[A/G]TTAGGCAGCATCAGC | 83860 |
rs778341059 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874204 | ATTTCAAGAAAGAGT[A/G]AAGAAACTTAAGGGC | 83860 |
rs778353062 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961882 | AAAAATAGGGTCTCG[C/T]TCTGTCGCCCAGGCT | 83860 |
rs778367053 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845723 | GTGGCTGTATAATCT[C/T]AGCATCATTTTCAAT | 83860 |
rs778382272 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7922385 | TGTGAATGTTGTACT[C/G]TCTTAATCTCATTCC | 83860 |
rs778382699 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857868 | AGAAACTCTCTTGAT[A/T]TTCAGCTATATCACA | 83860 |
rs778383041 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869752 | ACGGACTGCCTCCTT[C/G]CCTGTGCCTGCATCT | 83860 |
rs778414110 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7899340 | TGAGGTTGTGATGGT[A/C]ATCTGGGTGGCTGGC | 83860 |
rs778416448 | in-del | -/GG | 0.287134 | 0.247227 | intron-variant | TAF3 | GRCh38.p7 | 10:7824306 | TTGATTTGCTTTTCA[-/GG]CTTTGTTTCAGATGG | 83860 |
rs778433284 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947773 | TGGGGCTTTATTCCA[A/G]TGGTGACAGGAAGCA | 83860 |
rs778436214 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868368 | CAAGCTCTAGTAACC[A/T]TTCAGGAGTGGAGGT | 83860 |
rs778480897 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997209 | CGATAGTTTTTACCT[A/G]TGGCATCATTTTGTT | 83860 |
rs778483135 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973662 | CACATTGGGAATATA[A/G]CCAAGCACAATGCCT | 83860 |
rs778494419 | snp | C/T | 3.32679e-05 | 0.00407834 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964338 | AACAAAGACTAAAAC[C/T]AGCTCTCCAGGACAG | 83860 |
rs778494675 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846216 | CCCGCCTTGGCCTCC[C/T]GAAGTGCTGGCATTA | 83860 |
rs778498272 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7826397 | TGTAACTAAGATAAC[A/C]GGTTTAGATTAGGTA | 83860 |
rs778501476 | snp | C/T | 3.31214e-05 | 0.00406935 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824418 | TCACAACATTGAGCC[C/T]GTCACCTTCCCACAC | 83860 |
rs778524005 | in-del | -/TTAAA | 1.65649e-05 | 0.00287788 | frameshift-variant | TAF3 | GRCh38.p7 | 10:7824526 | AAAGAATACATTCCT[-/TTAAA]GATTACCTGCCACCC | 83860 |
rs778562066 | snp | A/G | 1.66707e-05 | 0.00288705 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965568 | GTTGCCAGTGCTTCC[A/G]GAAAAACTGTTTGAG | 83860 |
rs778564218 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939584 | AAGAAAACTACACAC[-/AC]ACACACACACACACA | 83860 |
rs778566549 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994238 | TGGTAAAAAAAAATT[C/G]CAGGTTTATCTTGCA | 83860 |
rs778575614 | snp | C/T | 1.66114e-05 | 0.00288192 | missense | TAF3 | GRCh38.p7 | 10:7964898 | CAAGTTCCGATAACT[C/T]ATGGACAATGGATGC | 83860 |
rs778578419 | snp | A/G | 1.848e-05 | 0.00303968 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7965703 | GAAGAGAGAGCGAGA[A/G]AAGAGAGAAAAAGAG | 83860 |
rs778602000 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7897702 | TTTTGAGACTCTCAC[C/T]CAGGTTGAGTGCAGT | 83860 |
rs778615174 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954876 | ATAGGTGAATGAGTG[A/G]ATTAGTTCTAGTTAA | 83860 |
rs778664440 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942675 | AAACACAGATCCCAA[A/G]AAGCGCTGGGGAATG | 83860 |
rs778708801 | snp | C/G | | | | | GRCh38.p7 | 10:7896096 | GTAACTGCATCGGTT[C/G]CTGCTGATAGGTCCC | 83860 |
rs778725578 | in-del | -/CAAAAAAAA | | | | | GRCh38.p7 | 10:7898545 | AACAAGACTCTGTCT[-/CAAAAAAAA]AAAAAAAAAAAAAAA | 83860 |
rs778747959 | snp | C/T | | | | | GRCh38.p7 | 10:7888071 | CAGCCAGCCGTCAAC[C/T]CTCATCCCCAGCTCT | 83860 |
rs778770145 | snp | C/T | 0.00091217 | 0.0213367 | intron-variant | TAF3 | GRCh38.p7 | 10:8009346 | GTGCGTACCTGCCGC[C/T]CGCGCGGTTAGCATG | 83860 |
rs778770722 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7852317 | CTCAAATGTTATAAA[C/T]GTTTGTTGGTTTATT | 83860 |
rs778787627 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7936182 | GCATTAGCTGTGTGC[A/G]CGTTGCTTTCAAGAC | 83860 |
rs778788960 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7905233 | GACCGTACAGAAACC[G/T]ACAAGTAGAGATGAA | 83860 |
rs778796618 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7872179 | AGTTTACCAGTAGAG[A/G]GCACTGTTGTAACAT | 83860 |
rs778829985 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7850963 | TGTGTGCCAGTCACT[A/G]TCATGAACACAGAAA | 83860 |
rs778860558 | in-del | -/TTTG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946932 | TTAAAAAAATAATTA[-/TTTG]TTTGTTTTTGGAGGC | 83860 |
rs778879008 | snp | C/T | | | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964731 | AGAGCCAGATCCTTT[C/T]GAATTTTCTTCTGGA | 83860 |
rs778880179 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7861158 | TTTAGTAGAGATTGG[G/T]TTTCACTGTGTTAGC | 83860 |
rs778933970 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7966280 | TAGCATCTTTTATTC[C/T]TTCCGTTTTCTGCTT | 83860 |
rs778935861 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910798 | TGAGCTCTAAACTGA[A/G]TTTATTTATTGTATA | 83860 |
rs778938075 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7982565 | ACCATGCCCGGCTAA[-/T]TTTTTTGTAGTTTTA | 83860 |
rs778952496 | snp | A/C/T | 3.4379e-05 | 0.00414588 | missense | TAF3 | GRCh38.p7 | 10:7964472 | AGAGCCCCAAGAGTC[A/C/T]CAAGAGCCCCAAGGT | 83860 |
rs778957981 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880431 | GAATTGGTGGATGTG[A/G]GAAATAAGAAATATG | 83860 |
rs778964499 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841847 | TGGACCTTATAGTCT[G/T]CAGGCAATCCTCTAA | 83860 |
rs778967296 | snp | A/G | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016564 | TGCACAAAAATGCGC[A/G]TTAGTGGTTTTTGGA | 83860 |
rs778973778 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919283 | TCAGTTTTCTGCAGG[-/C]CCCATCTGGGGCTTG | 83860 |
rs778994500 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854456 | TCTTAAGAAGTTAAC[-/A]ATGCTAAAGAGACAA | 83860 |
rs779029129 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7914103 | GGGAGTTTTTTTTTG[C/G]AATTTTTTGAGGAAA | 83860 |
rs779029520 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854807 | CAGTAGTATGTTACA[A/G]TAGCATGGAAGCCAT | 83860 |
rs779038149 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962154 | CCATGCCTGACCAGG[C/G]TCAAAGCTTTGAAAT | 83860 |
rs779051942 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885793 | CACCACCATCTTTTC[G/T]CTAAATGGAGGCTCC | 83860 |
rs779067249 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883007 | TATTTCAGTGGGTAC[C/T]TTCTAAAAGTGAGTG | 83860 |
rs779082865 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866530 | CTGAAGTGAGAGTCA[A/G]CTTGATGTTTTCAAG | 83860 |
rs779100423 | in-del | -/TGAG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926355 | CCTGCCATACTTGAT[-/TGAG]TAAAAGTTAAACTTC | 83860 |
rs779101859 | snp | A/G | 1.75993e-05 | 0.00296637 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7963936 | AGAAGAAGAAGAGCA[A/G]GTGCCCACTGATGGA | 83860 |
rs779142080 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947579 | TAGAGAGCCAAATAA[C/T]ACGAGAGAAGCAGCC | 83860 |
rs779147316 | snp | C/T | 1.6743e-05 | 0.0028933 | missense | TAF3 | GRCh38.p7 | 10:7964996 | TATATCTCTTCTCCG[C/T]CAGTGTCTCCTCCCA | 83860 |
rs779149721 | in-del | -/TGTATA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7937478 | TGCCTATTTGCCATC[-/TGTATA]TGTCTTTGGTAAAGT | 83860 |
rs779150105 | in-del | -/TG | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990036 | CCAGTTAAAATTAAC[-/TG]TGTATCTATTTTTAA | 83860 |
rs779159630 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830412 | TATCAGCCAAATGCG[C/T]ATCCCTAGACACATT | 83860 |
rs779174280 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7842608 | TGTCCGATGATACCT[A/G]ATGGTCACTATTGTC | 83860 |
rs779183016 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7962057 | GGTCTCACTATGTTG[C/T]CCAGGCTGGTTTCAA | 83860 |
rs779189771 | snp | A/C | 1.65957e-05 | 0.00288055 | missense | TAF3 | GRCh38.p7 | 10:7964073 | GTCCTGAAGCTGAAG[A/C]ACTGCCAGCCATGAA | 83860 |
rs779191572 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7926103 | TATAAATATTGAAGA[G/T]CTCTGATCTTTAAAA | 83860 |
rs779191734 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7938777 | AGAGATGAAACTGCC[A/G]AATGTTAAGTGTTGA | 83860 |
rs779192245 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7883906 | CCTTCTTGCTGGCGG[A/G]GAGAGGGGACTCTCA | 83860 |
rs779207198 | in-del | -/AAAGAT | 1.66545e-05 | 0.00288565 | cds-indel | TAF3 | GRCh38.p7 | 10:7965425 | GAGAAAGAAAAAGTG[-/AAAGAT]AAAGGCAGAGAAGAT | 83860 |
rs779228002 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7981935 | ACTTGTCTTTGAGTG[A/T]TCTAAACTTTTCCAG | 83860 |
rs779248214 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974744 | AGAGGTTGAAGAGAA[A/G]TTAAGAAAATGTTTA | 83860 |
rs779269056 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919823 | TGGAACCCACACATA[C/T]GGAGGGCTGACTGTG | 83860 |
rs779306877 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834999 | ATTATAGGTTCATCA[C/G]TTTTTTCGAGTGTGT | 83860 |
rs779308572 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7847806 | AGAGTTTCGCTCTGT[C/T]TTCCAGGCTGGAGTG | 83860 |
rs779319053 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961048 | GAAGATCACCGTAAG[A/G]CGACGTGAGAGATGG | 83860 |
rs779319629 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7918866 | GCAAGGAGGGATAGC[A/C]GGTGGAAGGAAGGAG | 83860 |
rs779320043 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894425 | GTTTGGAGAAGTTAG[G/T]TCACTGGTGGAGAGG | 83860 |
rs779339667 | snp | A/T | | | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817083 | CCCCTATACACAGAA[A/T]GGCAAATGAAGAGGA | 83860 |
rs779358007 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7846361 | CCCATTATATTCTGT[C/T]CTTTCATTTAAAATA | 83860 |
rs779369592 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888927 | TTCCTCCGGTGTATA[C/T]TGTGTCTTGAGAGAT | 83860 |
rs779371524 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875502 | GGTACAGAAGGATGT[A/G]TGGAAACCTCCACTG | 83860 |
rs779397742 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856860 | AACAGCTGGTTCTCA[-/AA]AAAAAAAAAAAAAAA | 83860 |
rs779398189 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007973 | GTGTGAAGAGGATGC[C/T]GTTAGTGGAGGAGCA | 83860 |
rs779399991 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009471 | TTTGAGACAGGGTCT[C/T]CCTGTGTGGCTCAGG | 83860 |
rs779423659 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7876560 | TATTGTCCACATAGG[A/C]GAAAGAGGAGAGAGG | 83860 |
rs779441787 | snp | A/C/G | 3.34226e-05 | 0.00408783 | missense | TAF3 | GRCh38.p7 | 10:7977259 | AAAGTGGAACCAGTC[A/C/G]CTCTGGCCCCGAGTC | 83860 |
rs779448207 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7994549 | AGATGAGGTCTCACT[G/T]TGTTGCCCAGGCTGG | 83860 |
rs779455303 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7974797 | AAGTGAGATGAAGGC[C/T]GGGCACAGTGGCTCA | 83860 |
rs779462028 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869133 | ATAAAAAATATTCTA[C/G]AAGATAGTAACTTTA | 83860 |
rs779465874 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870691 | ACACGCTTCTGAGTT[C/T]GCCTTCCTTCACTTC | 83860 |
rs779475324 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950280 | AGATAGAGAAATATA[A/G]AACGACCCAGGGAAG | 83860 |
rs779496738 | in-del | -/ACAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959162 | CACACACACACACAC[-/ACAAAA]AAAGTTTCAGGCTTT | 83860 |
rs779517111 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7997823 | AAAAATATAGAGAAG[C/T]AAAGCACCGTCTAGA | 83860 |
rs779524140 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903134 | GTAAGGTGGGAGGAT[C/T]GCTTGAGCCTAGAAA | 83860 |
rs779545168 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854923 | AAACACTTTTGACTT[A/C]TGGTTGAAGATGGAG | 83860 |
rs779551822 | in-del | -/TTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7892026 | ATTAACAGATAGATT[-/TTC]TTCTTTTAAAAATTT | 83860 |
rs779565635 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888976 | TAGGCTATAATTTAT[A/G]AGGATACATAGACAG | 83860 |
rs779591617 | snp | C/G | 3.91282e-05 | 0.00442296 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7818920 | GCCCCGGCAAGTCAA[C/G]GGTGACACCTTCGCT | 83860 |
rs779595470 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010705 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 83860 |
rs779618367 | snp | A/G | 1.66427e-05 | 0.00288462 | missense | TAF3 | GRCh38.p7 | 10:7965435 | AAGTGAAAGATAAAG[A/G]CAGAGAAGATAAGAT | 83860 |
rs779620031 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7822979 | TGGCTAGGCATGTTG[A/G]TGGTGCACTGGTAGT | 83860 |
rs779660538 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7880689 | CCATGCCTTTAAGTC[C/T]CTCATCTAGGTGGAT | 83860 |
rs779690573 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975898 | TGCAGCTAGTCAGTG[A/T]CTAACAGTAAACCAG | 83860 |
rs779691031 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7839480 | CAGAATAATGGAGGA[A/G]CAGTCGCAAAAATTA | 83860 |
rs779720837 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7829340 | TTATTAAGTGACGCC[C/T]GCACTGTATTGACAT | 83860 |
rs779721598 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7929292 | GTCTTCTAAAATCTA[-/T]TAATAGACTACCATT | 83860 |
rs779756772 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7874780 | ATTTCTTTTCTTTTC[C/T]AGGTGCAGATTACAT | 83860 |
rs779776091 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7919978 | AGGCTGGGTGTGGTG[G/T]CTCATGCTGGTAATC | 83860 |
rs779802903 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7890246 | TCTTCTTATCTGCCT[A/G]CTAAACTTCTGTATC | 83860 |
rs779803536 | snp | C/T | 1.66829e-05 | 0.00288811 | missense | TAF3 | GRCh38.p7 | 10:7965552 | CCATGCTGCCATCTT[C/T]GTTGCCAGTGCTTCC | 83860 |
rs779815417 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912259 | AAAATGATGGTTTAG[-/T]TTTTTTTATTAAAAA | 83860 |
rs779823339 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8009820 | TAGAAACGGTTTCAC[C/T]GTGTTAGCCAGGCTG | 83860 |
rs779862643 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955984 | TTGACAATTGTTCTG[C/T]AGTCACACTCTGATG | 83860 |
rs779893901 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7924619 | AATGCGCTATCTTGG[C/T]AGTGATCCTGTGAGT | 83860 |
rs779926088 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7867767 | AGTTGACCCTTGAAC[-/A]AATATGGGAGTTGGG | 83860 |
rs779943502 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7894206 | CTTAGGAATGTGGCA[C/T]ATTTTTTCCACTTCT | 83860 |
rs779988723 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7869975 | CTGAACTACTTTCGA[C/T]CCCAAGTTTTGCATA | 83860 |
rs779991090 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7955141 | TACCTAAATTCAGAC[A/G]AATAGAAAGGTATTT | 83860 |
rs779996282 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7912688 | TTTAGAGACTTTTGC[A/T]GATATCAGAGTTAGT | 83860 |
rs780083629 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8003829 | GGCAGGAGGATTGCT[A/T]GAGCCCAGGAGTTCA | 83860 |
rs780091934 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825028 | TTTTTTATCATGAGG[A/T]GCAATGTTTATTGTT | 83860 |
rs780095201 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959008 | AGCCGGGCGTGGTGA[C/T]GGGCGCCTGTAGTCT | 83860 |
rs780100455 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7987286 | ATGCCACTGCACACC[A/T]GCTTGGGCAATAGGA | 83860 |
rs780102460 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7840739 | GGACTTACTTTGTCT[C/T]GCTTTCTTGAATTTG | 83860 |
rs780108012 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886881 | AAAATTTTAAATACC[A/T]TCTCTAAGAGTATCT | 83860 |
rs780142236 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7942739 | GTGGGCAGCCGAGGC[A/G]TGTGGGCACGGAGTT | 83860 |
rs780143610 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946108 | GTCACTGCATCCTCT[A/G]CACAGCTGCTAGAGT | 83860 |
rs780178176 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940238 | TAGAATAGGGACATT[G/T]TAGACATGTGGAGTC | 83860 |
rs780201968 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991804 | CTTTTTTGAATTTTA[A/G]TATATTTTGAAGTGG | 83860 |
rs780214242 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921176 | TTGTTAATAATGTCT[A/G]CTATCTGAAATCTAA | 83860 |
rs780221043 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957635 | AATTTTTTAAATTTT[G/T]TTTTCAATATTTGTT | 83860 |
rs780251320 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7928923 | CTTATGTCAAAATTT[C/T]CATCTCCACAGAAGA | 83860 |
rs780255404 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007130 | TGTAAGTTTACAAGT[A/G]AATGTCTCCTACTTT | 83860 |
rs780256988 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8013889 | AGGCAGCATCAGCCG[C/T]TCCTGAGATGAAGCA | 83860 |
rs780261252 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010366 | ATACAGTAATATCAA[G/T]CTGTAAATGTAGAGA | 83860 |
rs780274046 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945555 | CACTCTCTAGATGCC[A/G]CAGGGAGGCCAGGCC | 83860 |
rs780279180 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7970544 | GCTTTGGTGACCTAA[C/G]TGACAAATGCAAATG | 83860 |
rs780295311 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864108 | CAGAGTCTGTAGTTT[C/T]CCTTAGGTTCACTCT | 83860 |
rs780295566 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | TAF3 | GRCh38.p7 | 10:7824459 | CATTTCCTGTTAGCA[A/G]GAACAATGTACTTCA | 83860 |
rs780321518 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832299 | ACATGTGGTATGTCT[C/T]CTTCTGTGCCTGGCT | 83860 |
rs780376074 | snp | A/G | 9.30362e-05 | 0.00681978 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009255 | CCTGCTGCCCTCCCC[A/G]GGTCCCGCCGCCTCC | 83860 |
rs780388820 | snp | G/T | 1.91042e-05 | 0.00309059 | intron-variant | TAF3 | GRCh38.p7 | 10:7965752 | GAAAAAGTAAGCAGT[G/T]TCTCATTTTTGGCCC | 83860 |
rs780391257 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7949152 | TGTGAGTGTCTGTGC[A/G]TGCACAGATGAAGAA | 83860 |
rs780394776 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7908141 | CTCCATTGCCATTTC[C/T]TCTTGTGTGTACATA | 83860 |
rs780398195 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871607 | TGCCACCATGCCTGG[C/T]TAATTTTTGTATTTT | 83860 |
rs780433401 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991189 | TATATGTATAGATAC[-/AC]ACACACACATATACA | 83860 |
rs780434889 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7927258 | CAAATTATTTTGTCC[A/G]TGGTGGCCATGTAAT | 83860 |
rs780445682 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996124 | ACTTAGTGATTTGAA[A/G]CAATAAACATCAGTT | 83860 |
rs780452764 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7904078 | GGGAAGCAGCAGTGC[A/T]AGAAGTAAGAAGAAG | 83860 |
rs780463254 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845076 | TTTCCAAAAGAGTTG[-/T]TATCAGTTTACAGTG | 83860 |
rs780484138 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7849196 | TTTTTTTCTTATAGA[G/T]GAGGGAAATAAAGTG | 83860 |
rs780486084 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825092 | GCTAATCAGGTATAA[C/T]GGTCAGTCCAATTGC | 83860 |
rs780522525 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7877913 | ATTTCTATACTGTAA[C/T]GGCAATTCAGATCTC | 83860 |
rs780524067 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7895875 | TGTCAGGGCTGCTTT[C/T]TCCCCACCCCTGCGC | 83860 |
rs780555849 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973911 | GAGGCAGGCAGATCA[C/T]GAGATCAGGAGTTTG | 83860 |
rs780557090 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7866686 | ACCATTGAAGAGTTT[A/T]AAGTTATTAGAAAGG | 83860 |
rs780578549 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907174 | GGATCTCCTGGAGTT[A/G]AAAGTAGGGGCACAG | 83860 |
rs780599837 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7983054 | TGGATGTGACTTCGG[C/T]GGGGCCACCTGCAGG | 83860 |
rs780630647 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8010979 | GACTGTTTTTTAGTT[G/T]CTTACTCCCTGAATA | 83860 |
rs780633447 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7933955 | TGTCATGACATGGTC[A/G]TCACCGCCTGCACAC | 83860 |
rs780653244 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993669 | TTTTCTTAAAGGGTA[C/T]TTTGCTGCTATATAC | 83860 |
rs780653252 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7984241 | TAGTTTTTACCCCGG[C/T]ACAATACTGTTTATT | 83860 |
rs780661861 | snp | A/G | 1.68917e-05 | 0.00290613 | missense | TAF3 | GRCh38.p7 | 10:7964564 | ACACTCAGTGAAAAA[A/G]TCAGTAAAGAGACTA | 83860 |
rs780667371 | snp | C/T | 9.92433e-05 | 0.00704356 | intron-variant | TAF3 | GRCh38.p7 | 10:7963900 | ATTTATTTTTTTCTT[C/T]CTTTTTCTTCCTTTA | 83860 |
rs780668229 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837729 | ACTCAGAGGCTGAGG[C/T]AGGGGGATCACTTGA | 83860 |
rs780723796 | snp | A/G | 1.66208e-05 | 0.00288273 | missense | TAF3 | GRCh38.p7 | 10:7964651 | CAGCCGAAAAAGGCT[A/G]TGGTAGCAGATAAAA | 83860 |
rs780740985 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7991270 | TGTGGTTTTGCTTCA[A/G]ACTCCCTTGGACACC | 83860 |
rs780787037 | snp | C/T | 0.000199068 | 0.00997468 | intron-variant | TAF3 | GRCh38.p7 | 10:8013708 | TCCCTCCATTTTTGC[C/T]GCTTCCGCTTTGCAA | 83860 |
rs780803211 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7977999 | TACAGTACTCTTACC[C/T]GATCCTAATAAGATA | 83860 |
rs780814065 | in-del | -/CAC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959161 | ACACACACACACACA[-/CAC]AAAAAAAGTTTCAGG | 83860 |
rs780828404 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7951461 | CCCGCAGGCTAACCT[A/G]GGCTCATTCCTGTGG | 83860 |
rs780830698 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7939076 | GATGATTGCTCTCCA[A/C]GAGTTCAGAAACAGG | 83860 |
rs780850499 | snp | C/G/T | 1.67806e-05 | 0.00289656 | missense | TAF3 | GRCh38.p7 | 10:7964437 | TGTATCCAAAGAAAA[C/G/T]AAATCACCTGGACGT | 83860 |
rs780868322 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7841076 | GGCTGGTCTGGAACT[C/T]CTGACCTCAGGTGAT | 83860 |
rs780874252 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7821267 | TTAGATATTTTTAGA[-/T]TTCTTTTTTCTATAC | 83860 |
rs780885664 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7837253 | CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 83860 |
rs780914766 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7920219 | TGATCACACCACTGC[A/G]CTCCGGCCTGCGCGA | 83860 |
rs780921561 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999834 | TTGACCCTGTCCTTG[G/T]TGGTCTGCTATGGAT | 83860 |
rs780942204 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7976726 | TTTCTTTTACAGCAT[G/T]TCAGATTGTTTTACC | 83860 |
rs780944359 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916810 | TAGGTTTCTTCTTTC[A/C]ACAATGGTGCTTTTC | 83860 |
rs780958822 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7998190 | TCTTGTCAACACTGA[G/T]TAGCCACTTTAATGT | 83860 |
rs780959213 | in-del | -/ATGT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7878703 | CCAATGTATGTATGT[-/ATGT]ATGTATGTATGTATG | 83860 |
rs780963416 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968774 | AGGCTGTCAGATGCT[A/G]TAATTTATGGTCCTC | 83860 |
rs780965185 | snp | A/G | 1.65869e-05 | 0.00287979 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7964098 | CATGAAGCGGCCTCG[A/G]CTATTAAGCACTAAA | 83860 |
rs780969796 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7921689 | GATTACTACAGAGAA[C/T]ATTTCAGGTAAGGTT | 83860 |
rs780979615 | snp | C/G | 1.658e-05 | 0.00287919 | missense | TAF3 | GRCh38.p7 | 10:7964207 | CTTTCTCCAGTCCAT[C/G]TACAGGACAGTACAG | 83860 |
rs781009187 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7945125 | ATGGGCAGCCTTTCC[C/T]GATGCACAGTCTGAA | 83860 |
rs781014042 | snp | C/T | | | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8016365 | TTTCTGCCATGAATG[C/T]TAAGTTGCAAATCAG | 83860 |
rs781018333 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7956172 | TTACAACTTTTCTAC[G/T]TTTGAAATTATTTCA | 83860 |
rs781021135 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7909224 | TAGGCTTACTGGATC[A/G]GAGCCTCTGGGGCCC | 83860 |
rs781034216 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7959702 | TGTATGAAACCATCC[C/G]AGTTTTCCTAGCCAA | 83860 |
rs781036124 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961871 | TTTTTTTCTTTAAAA[A/G]TAGGGTCTCGCTCTG | 83860 |
rs781043923 | snp | C/T | 1.65751e-05 | 0.00287876 | intron-variant | TAF3 | GRCh38.p7 | 10:8013859 | GCCCAGGGCGCCCTG[C/T]CGGCCACACTCATTA | 83860 |
rs781092249 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7901508 | AAACTACTTTCCTTT[C/G]AAATTGGGCTTGAGT | 83860 |
rs781120642 | in-del | -/TAGGC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7820944 | CCGTTAGTGATAGGC[-/TAGGC]TAGGCTAGGCTAGGC | 83860 |
rs781127552 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7871022 | TATAAGGAAAGACAA[C/T]GGAAAATTTTTAGTC | 83860 |
rs781140966 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7902746 | AATGTTCTGATCCTC[C/T]GCGTTCATTTAGCAT | 83860 |
rs781141417 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7889230 | TTAAATCTTAGTATT[A/G]CTAGGGTTTTGTCTT | 83860 |
rs781144788 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7943961 | TAATAGGGTTCTTTA[G/T]ACTTTGAAAAGGGGG | 83860 |
rs781150655 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7832386 | TTCCTTCTTTTTTTA[A/G]AGGCTGAATAATAAT | 83860 |
rs781167627 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7913804 | TAAACTGTTCTTGCC[A/G]AATACATTGAACCTG | 83860 |
rs781178983 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7870060 | TAGGAGAAATGAAAA[C/T]GGCTTGTATTAGTAT | 83860 |
rs781216058 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7990190 | TCTGTATATGAATAC[A/G]TGAGTTCTGCTAAAA | 83860 |
rs781223263 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007339 | AAAAGACAGCAAACA[G/T]TAATGCAGTATGTAT | 83860 |
rs781232634 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7947613 | AGCCGACCTGGAGGA[A/G]CAGCACTGGGGCTGC | 83860 |
rs781241908 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863249 | GCAGGGTTTTGTACT[A/G]GGACTGCATGGAACC | 83860 |
rs781251818 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830762 | GTGCTGGGATTCCAG[A/G]CGTGAGCCACCCCGC | 83860 |
rs781256399 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7875022 | TTTCTTTTGATACTC[A/G]ATTATAGATAGCAGT | 83860 |
rs781285475 | in-del | -/AGAGAAGAGAGAGCG | 1.84049e-05 | 0.00303349 | cds-indel | TAF3 | GRCh38.p7 | 10:7965685 | GAAGGAAAGAGAGAA[-/AGAGAAGAGAGAGCG]AGAGAAGAGAGAAAA | 83860 |
rs781293163 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7932838 | ATGCACTACCACACC[A/G]AGCTAATTCTTAAAT | 83860 |
rs781297726 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7833702 | GGCACGGGCCATGCA[A/G]CAACTAGCAAAGGCT | 83860 |
rs781308730 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7906500 | CTTTCGGAGGAGAAA[A/T]GCCAGAAAAATACAA | 83860 |
rs781320594 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925481 | TGACTTTGATTATTT[A/G]TAACAAACTTACATG | 83860 |
rs781329426 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865775 | CTGAGGTCAAACCTC[C/G]AACAGCAGCAGAGGA | 83860 |
rs781330557 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7985183 | CCACAAGTCTCAGCA[C/T]GTGGAACTGCCTCGC | 83860 |
rs781335118 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7980525 | TTCAAGATGACTTTC[C/T]AAGGACCTCAGATTC | 83860 |
rs781347791 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886460 | ATTTTTTTCTTTACA[C/G]AAAATATATAATAAC | 83860 |
rs781383507 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946238 | TCTTGACCTACCCAA[C/T]CCACCTCCTTTCCTC | 83860 |
rs781404813 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7957978 | TGACCAAATTTTGCA[-/G]GTTTTATAATACACA | 83860 |
rs781409246 | snp | A/G | 1.98151e-05 | 0.00314757 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8009153 | GAAGACCCCACCGCC[A/G]GCCCCCGCGCCCGCC | 83860 |
rs781427662 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825128 | TCCCTTTTTTCCTGC[A/G]TAATTTTAGATGTTG | 83860 |
rs781428667 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008753 | GTGGGGGTGGGGAGC[C/G]CCACCTCTGAAGCCG | 83860 |
rs781433885 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7845538 | AGGGTATGTGGAAGC[A/G]AGAATGTGTTTGAGA | 83860 |
rs781441663 | snp | C/T | 8.99159e-05 | 0.00670447 | utr-variant-3-prime | TAF3 | GRCh38.p7 | 10:8014803 | GGGCTTCTTCCCTGG[C/T]GCCTCTGGAAGGGAG | 83860 |
rs781505085 | snp | C/T | 1.65633e-05 | 0.00287774 | intron-variant | TAF3 | GRCh38.p7 | 10:7824310 | ATTTGCTTTTCACTT[C/T]GTTTCAGATGGCCGA | 83860 |
rs781547243 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7931972 | AAAGTGCTAGAGATA[C/T]GCAACCAGAATATAT | 83860 |
rs781547611 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907319 | AGGTCTTTGAAATCC[A/G]GCATTGCCCAAAGTG | 83860 |
rs781553711 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7825223 | ACGATATTTTTTCTT[A/G]TAAGAGTTGGAAAAG | 83860 |
rs781591712 | snp | A/G | 0.00011592 | 0.00761226 | synonymous-codon | TAF3 | GRCh38.p7 | 10:7824442 | CCCACACCAAATTCC[A/G]TCATTTCCTGTTAGC | 83860 |
rs781598649 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7940168 | CCATCAGAATTTTGA[G/T]TGAAATAATTTCAAC | 83860 |
rs781606265 | snp | A/G | 2.03089e-05 | 0.00318654 | synonymous-codon | TAF3 | GRCh38.p7 | 10:8014679 | CCCAGAAGAGATGCA[A/G]TGGTTCTGCCCCAAG | 83860 |
rs781607179 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7834567 | AGATGTGTGTGAATA[A/G]ATAGATAGGTGGATA | 83860 |
rs781617271 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:8004891 | CCATTTTTCTTCTAG[A/C]ATTATGATCAAACAT | 83860 |
rs781623968 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7843782 | ATCAGACTTGGTTTA[A/C]ATTTATAATTCATTT | 83860 |
rs781636314 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7910203 | AGTTCCTCAGTCCCT[C/T]CTTATACTGAGCACT | 83860 |
rs781639995 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7888124 | GTCGCCTGCAAGCAC[A/G]CTCAGATCTCTCCCA | 83860 |
rs781689031 | snp | G/T | 1.66048e-05 | 0.00288134 | missense | TAF3 | GRCh38.p7 | 10:7964874 | CTCTGCCTCTTTCCG[G/T]TGGAACCTCAAGTTC | 83860 |
rs781700965 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7903545 | ATTTAATATGTTTTT[-/A]ATCTTAGGAAATAAC | 83860 |
rs781736644 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7971649 | TTTATAGATAAGCTT[G/T]TTAAAAATCCACCTC | 83860 |
rs781736731 | snp | A/C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7857351 | TACATAGTTTTATCC[A/C/G]ATTAGCAAGTTAGAG | 83860 |
rs781741557 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7952396 | ATAGGAGATGTTGTC[A/G]TTATCATAAATCATA | 83860 |
rs796066107 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975080 | TGTCTCAAAAAAAAA[-/AAAAAAAAAAAAA]GAGTGAGATGAAAAT | 83860 |
rs796131325 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7865522 | AAACAAACAGAAAGT[-/A]GGGGAGCAAGCTGCC | 83860 |
rs796147474 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7946054 | CCTGCCTTGGCCTCC[G/T]CTGTGGGGCTGAAGC | 83860 |
rs796150084 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7967238 | TAGTCATTTATCCCT[-/T]GTGTACCTAGTAAGT | 83860 |
rs796202454 | in-del | -/TT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7864823 | GAAATATAGTTTATC[-/TT]TTTTTTTTTCCTTTT | 83860 |
rs796207642 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7979376 | TGAAAAAAAAAAAAA[-/A]GGCATTGATAGTTAT | 83860 |
rs796209179 | in-del | -/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7881262 | AAAACAAAAAAAAAA[-/C]CCCACAAGCTCTTTT | 83860 |
rs796225948 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7953898 | CTCCATAGTGAGATT[C/T]AGAGTGCACTCCATA | 83860 |
rs796233010 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7896302 | ACGTAGACCAAAACC[-/A]ATTCTTGCCAGAACC | 83860 |
rs796251046 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925813 | CAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAG | 83860 |
rs796272253 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7993457 | TTGCTGAGATTATAG[A/G]CGTGAGCCACCATGC | 83860 |
rs796279577 | in-del | -/ATAT | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863693 | TATATATACACACAC[-/ATAT]ATATATATACACATA | 83860 |
rs796312907 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7925814 | AAAAAAAAAAAAAAG[-/A]AAAGAAAAGAAAAGA | 83860 |
rs796350497 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7860276 | CCAGACCCTGTCTGG[-/A]AAAAAAAAAAGAAGA | 83860 |
rs796412496 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7973636 | GTTTGTTTTTTAAAA[A/T]CCTTAATGAGCACAT | 83860 |
rs796425365 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7855941 | GAAAAAAAAAAAGAC[-/A]AAAAAAAAAATAAGC | 83860 |
rs796433303 | snp | G/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8001271 | TCTCCCTTTCCCCTA[G/T]CCTGACAGTACCAGG | 83860 |
rs796448104 | in-del | AAGCA/GATTTTAATAGAAGCTCCACATATCTTG | | | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819685 | ATCTTGTTGATGTGA[lengthTooLong]TGTATGTGTGTTTGT | 83860 |
rs796448568 | in-del | -/AA | | | intron-variant | TAF3 | GRCh38.p7 | 10:7856859 | TAACAGCTGGTTCTC[-/AA]AAAAAAAAAAAAAAA | 83860 |
rs796467114 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7950159 | GACAAGAAATGCATG[A/G]ACAGTCAAACAGTTA | 83860 |
rs796487184 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7907926 | ACCAGCAGGAGTCGA[C/T]GGGGACTGAATCTGG | 83860 |
rs796495070 | snp | A/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7887605 | AAGTGTGAACTGTTT[A/T]GGCAAGATGAATTGA | 83860 |
rs796518358 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7868772 | GTACCAAGTAAACAA[A/G]AACAGTAATACATTT | 83860 |
rs796535778 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007539 | CCTAACTGTCTGTTA[-/T]ATTGTTTTCTCTGTG | 83860 |
rs796557302 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7978026 | ATAATGAAACATTGA[-/T]TTTTTTTTTTTGGAA | 83860 |
rs796636827 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7863907 | ACATGGCATACATAG[C/T]TTTTTTCTTTAACAA | 83860 |
rs796642954 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7916943 | TTTCTTCAGAAATAT[A/G]GACTGTCTGTTGTGT | 83860 |
rs796648092 | in-del | -/TGGGAGGCCGAGA | | | intron-variant | TAF3 | GRCh38.p7 | 10:8000524 | GCAATCTCAGCACTT[-/TGGGAGGCCGAGA]TGGGAGGATCACTTG | 83860 |
rs796665151 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7961116 | AAGGTCCTTGCAGCC[A/G]TACAGAGAAGAGGTG | 83860 |
rs796788234 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7886640 | AAACTAAGTGAAATA[A/C]CATATATACATCATA | 83860 |
rs796792783 | in-del | -/A | | | intron-variant | TAF3 | GRCh38.p7 | 10:7954916 | TCCATAGTGAGATTC[-/A]AGAGTGCACTCCATA | 83860 |
rs796793794 | in-del | -/AC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7885250 | GTTATATAAATTTTG[-/AC]ACACACACACACACA | 83860 |
rs796798289 | in-del | -/TTTC | | | intron-variant | TAF3 | GRCh38.p7 | 10:7999463 | AAGAAAGAAGTTTTT[-/TTTC]TTTTTTTTTTTGAGA | 83860 |
rs796809255 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7968139 | AAAGGTTAAACTAAA[A/G]TGAGACATATCTGCT | 83860 |
rs796851580 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7873626 | GAGTTCTCCCCCCCC[C/T]CCCGTCAAAAGGGGG | 83860 |
rs796863121 | in-del | -/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008083 | CTCTGCAGCCCGTCT[-/G]GGAACAATCTTTTTT | 83860 |
rs796889732 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7854084 | TTTACCAGCATATCT[C/T]TCAATACACTTGCAA | 83860 |
rs796913836 | in-del | GTTG/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7838365 | CAGTTTTGTTTTTTT[GTTG/T]TGTTGTTGTTGTTTG | 83860 |
rs797003431 | in-del | -/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7996616 | TGACATTTCAATGTC[-/T]TTTTTTTTTTGTATT | 83860 |