Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9014 |
| ensemblid | ENSG00000115750.17 |
| hgncid | 11533 |
| symbol | TAF1B |
| name | TATA-box binding protein associated factor, RNA polymerase I subunit B |
| refseq_nuc | NM_005680.3 |
| refseq_prot | NP_005671.3 |
| ensembl_nuc | ENST00000263663.10 |
| ensembl_prot | ENSP00000263663.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 9843474 |
| end | 9934416 |
| strand | + |
| ver | v1.2 |
| region | chr2:9843474-9934416 |
| region5000 | chr2:9838474-9939416 |
| regionname0 | TAF1B_chr2_9843474_9934416 |
| regionname5000 | TAF1B_chr2_9838474_9939416 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 588 | 81 | 1 | 16 | 54 | 2 | 8 | 47 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0002 | 0/1 | 588 | 69 | 14 | 18 | 21 | 3 | 12 | 17 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0003 | 0/0 | 588 | 60 | 33 | 9 | 12 | 1 | 5 | 9 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0004 | 0/0 | 588 | 59 | 0 | 12 | 38 | 3 | 6 | 28 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0005 | 0/0 | 588 | 57 | 20 | 5 | 26 | 2 | 4 | 16 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0006 | 1/0 | 588 | 22 | 20 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0007 | 0/0 | 588 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0008 | 0/0 | 588 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0009 | 0/0 | 588 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0010 | 0/0 | 588 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0011 | 0/0 | 588 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0012 | 0/0 | 588 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0013 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | MDVEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0014 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0015 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| a0016 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | MDLEE others(583): Show |
chr2 | 9838474 | 9939416 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1764 | 80 | 1 | 16 | 54 | 2 | 7 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0001c0020 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0002c0002 | 0/1 | 1764 | 69 | 14 | 18 | 21 | 3 | 12 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0003c0004 | 0/0 | 1764 | 58 | 33 | 9 | 10 | 1 | 5 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0003c0016 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0004c0003 | 0/0 | 1764 | 59 | 0 | 12 | 38 | 3 | 6 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0005c0005 | 0/0 | 1764 | 40 | 6 | 3 | 26 | 2 | 3 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0005c0007 | 0/0 | 1764 | 14 | 12 | 1 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0005c0011 | 0/0 | 1764 | 3 | 2 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0006c0006 | 1/0 | 1764 | 20 | 18 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0006c0015 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0007c0008 | 0/0 | 1764 | 6 | 0 | 0 | 6 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0008c0009 | 0/0 | 1764 | 4 | 0 | 2 | 0 | 2 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0009c0012 | 0/0 | 1764 | 3 | 0 | 1 | 0 | 1 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0010c0014 | 0/0 | 1764 | 3 | 2 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0011c0010 | 0/0 | 1764 | 3 | 2 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0012c0013 | 0/0 | 1764 | 3 | 0 | 0 | 3 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0013c0021 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0014c0017 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0015c0019 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 | ||
| a0016c0018 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | ATGGA others(1759): Show |
chr2 | 9838474 | 9939416 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2267 | 11 | 0 | 6 | 3 | 1 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0001c0001t0002 | 0/0 | 2267 | 67 | 1 | 10 | 50 | 1 | 5 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0001c0001t0006 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0001c0001t0007 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0001c0020t0002 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0002c0002t0001 | 0/1 | 2267 | 61 | 13 | 12 | 20 | 3 | 12 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0002c0002t0002 | 0/0 | 2267 | 8 | 1 | 6 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0003c0004t0001 | 0/0 | 2267 | 54 | 33 | 9 | 6 | 1 | 5 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0003c0004t0004 | 0/0 | 2267 | 4 | 0 | 0 | 4 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0003c0016t0001 | 0/0 | 2267 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0004c0003t0001 | 0/0 | 2267 | 56 | 0 | 9 | 38 | 3 | 6 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0004c0003t0005 | 0/0 | 2267 | 3 | 0 | 3 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0005c0005t0001 | 0/0 | 2267 | 40 | 6 | 3 | 26 | 2 | 3 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0005c0007t0001 | 0/0 | 2267 | 14 | 12 | 1 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0005c0011t0001 | 0/0 | 2267 | 3 | 2 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0006c0006t0001 | 1/0 | 2267 | 15 | 14 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0006c0006t0003 | 0/0 | 2267 | 5 | 4 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0006c0015t0001 | 0/0 | 2267 | 2 | 2 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0007c0008t0001 | 0/0 | 2267 | 6 | 0 | 0 | 6 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0008c0009t0001 | 0/0 | 2267 | 4 | 0 | 2 | 0 | 2 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0009c0012t0001 | 0/0 | 2267 | 3 | 0 | 1 | 0 | 1 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0010c0014t0001 | 0/0 | 2267 | 3 | 2 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0011c0010t0001 | 0/0 | 2267 | 3 | 2 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0012c0013t0001 | 0/0 | 2267 | 3 | 0 | 0 | 3 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0013c0021t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0014c0017t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0015c0019t0001 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| a0016c0018t0001 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | CTTTC others(2262): Show |
chr2 | 9838474 | 9939416 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0001c0020t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0004t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0016t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0003c0016t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0004c0003t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0005t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0007t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0011t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0011t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0005c0011t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0003g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0006t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0015t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0006c0015t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0007c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0007c0008t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0007c0008t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0007c0008t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0007c0008t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0007c0008t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0008c0009t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0008c0009t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0008c0009t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0008c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0009c0012t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0009c0012t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0009c0012t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0010c0014t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0010c0014t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0010c0014t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0011c0010t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0011c0010t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0011c0010t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0012c0013t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0012c0013t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0012c0013t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0013c0021t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0014c0017t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0015c0019t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| a0016c0018t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0009 | c0012 | t0001 | g0348 | EUR | GBR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00099 | hp2 | a0004 | c0003 | t0001 | g0258 | EUR | GBR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00140 | hp1 | a0004 | c0003 | t0001 | g0009 | EUR | GBR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0127 | EUR | FIN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0147 | EUR | FIN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00323 | hp2 | a0004 | c0003 | t0001 | g0266 | EUR | FIN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00438 | hp1 | a0005 | c0005 | t0001 | g0101 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00438 | hp2 | a0004 | c0003 | t0001 | g0034 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00597 | hp1 | a0005 | c0005 | t0001 | g0082 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00597 | hp2 | a0004 | c0003 | t0001 | g0242 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00609 | hp2 | a0003 | c0016 | t0001 | g0259 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00621 | hp2 | a0004 | c0003 | t0001 | g0240 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00639 | hp1 | a0003 | c0004 | t0001 | g0293 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00639 | hp2 | a0010 | c0014 | t0001 | g0337 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00673 | hp1 | a0004 | c0003 | t0001 | g0262 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | CHS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG00741 | hp2 | a0003 | c0004 | t0001 | g0260 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01069 | hp1 | a0008 | c0009 | t0001 | g0038 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01070 | hp1 | a0005 | c0011 | t0001 | g0351 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01071 | hp1 | a0008 | c0009 | t0001 | g0054 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01106 | hp1 | a0004 | c0003 | t0001 | g0251 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01109 | hp1 | a0006 | c0006 | t0003 | g0001 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01109 | hp2 | a0011 | c0010 | t0001 | g0352 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01167 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01168 | hp2 | a0009 | c0012 | t0001 | g0347 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01175 | hp2 | a0003 | c0004 | t0001 | g0278 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01192 | hp2 | a0004 | c0003 | t0001 | g0330 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01256 | hp1 | a0004 | c0003 | t0001 | g0042 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01256 | hp2 | a0005 | c0005 | t0001 | g0085 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01257 | hp2 | a0005 | c0005 | t0001 | g0102 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01346 | hp1 | a0003 | c0004 | t0001 | g0297 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01361 | hp1 | a0003 | c0004 | t0001 | g0328 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01433 | hp1 | a0005 | c0005 | t0001 | g0089 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01433 | hp2 | a0004 | c0003 | t0001 | g0264 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01496 | hp1 | a0005 | c0007 | t0001 | g0339 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01496 | hp2 | a0004 | c0003 | t0001 | g0032 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01516 | hp1 | a0008 | c0009 | t0001 | g0055 | EUR | IBS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01516 | hp2 | a0003 | c0004 | t0001 | g0283 | EUR | IBS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01517 | hp1 | a0008 | c0009 | t0001 | g0053 | EUR | IBS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01517 | hp2 | a0005 | c0005 | t0001 | g0090 | EUR | IBS | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01884 | hp1 | a0003 | c0004 | t0001 | g0301 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01884 | hp2 | a0005 | c0007 | t0001 | g0011 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01928 | hp2 | a0004 | c0003 | t0001 | g0250 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0338 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01952 | hp2 | a0004 | c0003 | t0001 | g0231 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01975 | hp1 | a0004 | c0003 | t0005 | g0233 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02004 | hp1 | a0004 | c0003 | t0005 | g0234 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02004 | hp2 | a0003 | c0004 | t0001 | g0286 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02015 | hp1 | a0004 | c0003 | t0001 | g0332 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02015 | hp2 | a0005 | c0005 | t0001 | g0077 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02027 | hp1 | a0003 | c0004 | t0001 | g0288 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02027 | hp2 | a0005 | c0005 | t0001 | g0105 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02055 | hp1 | a0006 | c0006 | t0001 | g0031 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0336 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02056 | hp1 | a0004 | c0003 | t0001 | g0268 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02056 | hp2 | a0005 | c0005 | t0001 | g0092 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02074 | hp1 | a0005 | c0005 | t0001 | g0098 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02080 | hp1 | a0005 | c0005 | t0001 | g0100 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02080 | hp2 | a0004 | c0003 | t0001 | g0219 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02083 | hp2 | a0004 | c0003 | t0001 | g0270 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02135 | hp1 | a0005 | c0005 | t0001 | g0094 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02135 | hp2 | a0003 | c0004 | t0001 | g0289 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02145 | hp1 | a0003 | c0004 | t0001 | g0342 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02165 | hp1 | a0004 | c0003 | t0001 | g0241 | EAS | CDX | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CDX | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02257 | hp1 | a0013 | c0021 | t0001 | g0023 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02257 | hp2 | a0003 | c0004 | t0001 | g0306 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0359 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02258 | hp2 | a0003 | c0004 | t0001 | g0294 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0123 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02273 | hp2 | a0004 | c0003 | t0001 | g0263 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0276 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0117 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02293 | hp2 | a0004 | c0003 | t0005 | g0235 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02300 | hp2 | a0004 | c0003 | t0001 | g0227 | AMR | PEL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02451 | hp1 | a0005 | c0007 | t0001 | g0073 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02451 | hp2 | a0006 | c0006 | t0001 | g0014 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02523 | hp2 | a0005 | c0005 | t0001 | g0088 | EAS | KHV | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0322 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02572 | hp2 | a0005 | c0007 | t0001 | g0011 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02602 | hp1 | a0003 | c0004 | t0001 | g0295 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02615 | hp1 | a0005 | c0007 | t0001 | g0341 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02615 | hp2 | a0006 | c0006 | t0001 | g0026 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02622 | hp1 | a0005 | c0007 | t0001 | g0333 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0312 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02630 | hp1 | a0003 | c0004 | t0001 | g0302 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02630 | hp2 | a0006 | c0006 | t0003 | g0001 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02647 | hp1 | a0005 | c0005 | t0001 | g0013 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02647 | hp2 | a0006 | c0006 | t0003 | g0001 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02698 | hp1 | a0005 | c0007 | t0001 | g0132 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0303 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02717 | hp2 | a0005 | c0007 | t0001 | g0340 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02723 | hp1 | a0005 | c0007 | t0001 | g0059 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0307 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02735 | hp2 | a0003 | c0004 | t0001 | g0296 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02738 | hp1 | a0003 | c0004 | t0001 | g0287 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0201 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02809 | hp1 | a0003 | c0004 | t0001 | g0308 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02809 | hp2 | a0003 | c0004 | t0001 | g0309 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02818 | hp1 | a0006 | c0006 | t0003 | g0012 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02818 | hp2 | a0005 | c0007 | t0001 | g0057 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0300 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02895 | hp2 | a0006 | c0006 | t0001 | g0015 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02896 | hp1 | a0003 | c0004 | t0001 | g0044 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02896 | hp2 | a0005 | c0005 | t0001 | g0093 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02897 | hp1 | a0005 | c0005 | t0001 | g0084 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0299 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02922 | hp1 | a0006 | c0006 | t0001 | g0019 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02965 | hp1 | a0011 | c0010 | t0001 | g0353 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02965 | hp2 | a0003 | c0004 | t0001 | g0304 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0323 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02970 | hp2 | a0006 | c0015 | t0001 | g0016 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0335 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02976 | hp2 | a0010 | c0014 | t0001 | g0072 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03041 | hp1 | a0005 | c0007 | t0001 | g0334 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03041 | hp2 | a0005 | c0011 | t0001 | g0349 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03130 | hp1 | a0003 | c0004 | t0001 | g0319 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03130 | hp2 | a0011 | c0010 | t0001 | g0354 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03139 | hp1 | a0005 | c0007 | t0001 | g0052 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03139 | hp2 | a0006 | c0006 | t0001 | g0022 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0321 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03195 | hp2 | a0003 | c0004 | t0001 | g0314 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0279 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03209 | hp2 | a0005 | c0011 | t0001 | g0350 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0358 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0325 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03239 | hp2 | a0003 | c0004 | t0001 | g0327 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0324 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0357 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03486 | hp1 | a0003 | c0004 | t0001 | g0320 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03486 | hp2 | a0006 | c0006 | t0001 | g0027 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03491 | hp2 | a0005 | c0005 | t0001 | g0087 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03516 | hp1 | a0005 | c0007 | t0001 | g0058 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03516 | hp2 | a0006 | c0006 | t0001 | g0028 | AFR | ESN | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03540 | hp1 | a0005 | c0007 | t0001 | g0056 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03540 | hp2 | a0006 | c0006 | t0001 | g0025 | AFR | GWD | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03579 | hp1 | a0005 | c0005 | t0001 | g0033 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0292 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03688 | hp1 | a0005 | c0005 | t0001 | g0083 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03704 | hp1 | a0004 | c0003 | t0001 | g0043 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03831 | hp1 | a0004 | c0003 | t0001 | g0249 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03927 | hp1 | a0003 | c0004 | t0001 | g0253 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03927 | hp2 | a0004 | c0003 | t0001 | g0290 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03942 | hp1 | a0004 | c0003 | t0001 | g0009 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04115 | hp2 | a0005 | c0005 | t0001 | g0095 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04184 | hp2 | a0004 | c0003 | t0001 | g0256 | SAS | BEB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04199 | hp2 | a0001 | c0020 | t0002 | g0169 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04204 | hp2 | a0004 | c0003 | t0001 | g0226 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | STU | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18522 | hp1 | a0003 | c0004 | t0001 | g0313 | AFR | YRI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18522 | hp2 | a0014 | c0017 | t0001 | g0071 | AFR | YRI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18612 | hp2 | a0005 | c0005 | t0001 | g0108 | EAS | CHB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18747 | hp2 | a0004 | c0003 | t0001 | g0239 | EAS | CHB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0326 | AFR | YRI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0355 | AFR | YRI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18940 | hp1 | a0005 | c0005 | t0001 | g0343 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18941 | hp2 | a0004 | c0003 | t0001 | g0247 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18945 | hp1 | a0003 | c0004 | t0001 | g0285 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18946 | hp2 | a0007 | c0008 | t0001 | g0229 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18947 | hp1 | a0007 | c0008 | t0001 | g0230 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18948 | hp1 | a0012 | c0013 | t0001 | g0051 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18950 | hp1 | a0004 | c0003 | t0001 | g0255 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18957 | hp1 | a0005 | c0005 | t0001 | g0109 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18957 | hp2 | a0004 | c0003 | t0001 | g0232 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18959 | hp1 | a0012 | c0013 | t0001 | g0037 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18959 | hp2 | a0003 | c0004 | t0001 | g0284 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18960 | hp1 | a0003 | c0004 | t0001 | g0280 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18961 | hp2 | a0005 | c0005 | t0001 | g0075 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18962 | hp1 | a0007 | c0008 | t0001 | g0236 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18965 | hp2 | a0004 | c0003 | t0001 | g0221 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18968 | hp2 | a0005 | c0005 | t0001 | g0104 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18970 | hp2 | a0004 | c0003 | t0001 | g0218 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18971 | hp1 | a0004 | c0003 | t0001 | g0222 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18972 | hp2 | a0004 | c0003 | t0001 | g0257 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18973 | hp2 | a0005 | c0005 | t0001 | g0096 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18974 | hp2 | a0003 | c0016 | t0001 | g0207 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18977 | hp2 | a0004 | c0003 | t0001 | g0275 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18980 | hp2 | a0004 | c0003 | t0001 | g0272 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18982 | hp1 | a0015 | c0019 | t0001 | g0237 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18982 | hp2 | a0003 | c0004 | t0001 | g0282 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18983 | hp2 | a0004 | c0003 | t0001 | g0271 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18984 | hp1 | a0003 | c0004 | t0004 | g0245 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18984 | hp2 | a0004 | c0003 | t0001 | g0317 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18986 | hp2 | a0004 | c0003 | t0001 | g0228 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18988 | hp1 | a0007 | c0008 | t0001 | g0252 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18989 | hp1 | a0004 | c0003 | t0001 | g0220 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18992 | hp1 | a0016 | c0018 | t0001 | g0078 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18994 | hp1 | a0004 | c0003 | t0001 | g0248 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18995 | hp1 | a0005 | c0005 | t0001 | g0076 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18998 | hp1 | a0004 | c0003 | t0001 | g0265 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18998 | hp2 | a0005 | c0005 | t0001 | g0099 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18999 | hp2 | a0004 | c0003 | t0001 | g0254 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19002 | hp2 | a0004 | c0003 | t0001 | g0246 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19003 | hp2 | a0004 | c0003 | t0001 | g0274 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19010 | hp1 | a0003 | c0004 | t0004 | g0329 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19011 | hp2 | a0004 | c0003 | t0001 | g0216 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19030 | hp1 | a0010 | c0014 | t0001 | g0074 | AFR | LWK | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0310 | AFR | LWK | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | LWK | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19043 | hp2 | a0006 | c0006 | t0001 | g0029 | AFR | LWK | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19054 | hp2 | a0004 | c0003 | t0001 | g0223 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19058 | hp2 | a0004 | c0003 | t0001 | g0269 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19060 | hp1 | a0005 | c0005 | t0001 | g0080 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19065 | hp1 | a0005 | c0005 | t0001 | g0097 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19065 | hp2 | a0003 | c0004 | t0004 | g0316 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19068 | hp2 | a0004 | c0003 | t0001 | g0291 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19070 | hp1 | a0005 | c0005 | t0001 | g0110 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19070 | hp2 | a0004 | c0003 | t0001 | g0217 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19074 | hp2 | a0004 | c0003 | t0001 | g0273 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19076 | hp2 | a0007 | c0008 | t0001 | g0244 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19080 | hp1 | a0005 | c0005 | t0001 | g0091 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19080 | hp2 | a0004 | c0003 | t0001 | g0225 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19081 | hp2 | a0005 | c0005 | t0001 | g0107 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19082 | hp2 | a0005 | c0005 | t0001 | g0106 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19083 | hp2 | a0004 | c0003 | t0001 | g0267 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19084 | hp2 | a0005 | c0005 | t0001 | g0086 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19085 | hp1 | a0005 | c0005 | t0001 | g0344 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19086 | hp1 | a0007 | c0008 | t0001 | g0243 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19088 | hp1 | a0004 | c0003 | t0001 | g0224 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19088 | hp2 | a0012 | c0013 | t0001 | g0045 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19090 | hp1 | a0005 | c0005 | t0001 | g0079 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19091 | hp1 | a0003 | c0004 | t0004 | g0315 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19240 | hp1 | a0006 | c0006 | t0001 | g0018 | AFR | YRI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA19240 | hp2 | a0006 | c0006 | t0003 | g0001 | AFR | YRI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20129 | hp1 | a0006 | c0006 | t0001 | g0021 | AFR | ASW | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20129 | hp2 | a0006 | c0006 | t0001 | g0020 | AFR | ASW | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20805 | hp1 | a0005 | c0005 | t0001 | g0070 | EUR | TSI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0062 | EUR | TSI | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20905 | hp1 | a0009 | c0012 | t0001 | g0346 | SAS | GIH | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | GIH | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01123 | hp1 | a0003 | c0004 | t0001 | g0281 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02109 | hp1 | a0003 | c0004 | t0001 | g0277 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0305 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG02559 | hp2 | a0005 | c0005 | t0001 | g0081 | AFR | ACB | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03471 | hp1 | a0003 | c0004 | t0001 | g0298 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG03471 | hp2 | a0003 | c0004 | t0001 | g0311 | AFR | MSL | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG06807 | hp1 | a0005 | c0005 | t0001 | g0103 | AFR | USA | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| HG06807 | hp2 | a0006 | c0006 | t0001 | g0024 | AFR | USA | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18955 | hp1 | a0004 | c0003 | t0001 | g0238 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20300 | hp1 | a0006 | c0015 | t0001 | g0017 | AFR | USA | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0136 | AFR | USA | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0356 | AFR | LWK | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| NA21309 | hp2 | a0003 | c0004 | t0001 | g0318 | AFR | LWK | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0126 | REF | REF | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| homoSapiens | grch38p0 | a0006 | c0006 | t0001 | g0030 | REF | REF | TAF1B_chr2_9838474_9939416 | TAF1B | chr2 | 9838474 | 9939416 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9843548 | C | G | 1 | a0013 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.7C>G | p.Leu3Val | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/15 | 75/2267 | 7/1767 | 3/588 | chr2 | 9843548 | |||
| chr2:9843557 | G | T | 5 | a0001 a0003 a0004 others(2): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
missense_variant&splice_region_variant | MODERATE | c.16G>T | p.Ala6Ser | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/15 | 84/2267 | 16/1767 | 6/588 | chr2 | 9843557 | |||
| chr2:9868385 | T | C | 1 | a0015 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.509T>C | p.Ile170Thr | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/15 | 577/2267 | 509/1767 | 170/588 | chr2 | 9868385 | |||
| chr2:9904870 | C | G | 1 | a0008 | 4 | HG01069.hp1 HG01071.hp1 HG01516.hp1 others(1): Show |
missense_variant | MODERATE | c.819C>G | p.Asp273Glu | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/15 | 887/2267 | 819/1767 | 273/588 | chr2 | 9904870 | |||
| chr2:9904895 | G | A | 14 | a0001 a0002 a0003 others(11): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
missense_variant | MODERATE | c.844G>A | p.Val282Ile | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/15 | 912/2267 | 844/1767 | 282/588 | chr2 | 9904895 | |||
| chr2:9904926 | G | A | 1 | a0011 | 3 | HG01109.hp2 HG02965.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.875G>A | p.Arg292His | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/15 | 943/2267 | 875/1767 | 292/588 | chr2 | 9904926 | |||
| chr2:9910748 | G | A | 1 | a0009 | 3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.968G>A | p.Ser323Asn | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/15 | 1036/2267 | 968/1767 | 323/588 | chr2 | 9910748 | |||
| chr2:9910831 | A | G | 6 | a0001 a0002 a0008 others(3): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
missense_variant | MODERATE | c.1051A>G | p.Thr351Ala | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/15 | 1119/2267 | 1051/1767 | 351/588 | chr2 | 9910831 | |||
| chr2:9913230 | T | C | 1 | a0012 | 3 | NA18948.hp1 NA18959.hp1 NA19088.hp2 |
missense_variant | MODERATE | c.1252T>C | p.Trp418Arg | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/15 | 1320/2267 | 1252/1767 | 418/588 | chr2 | 9913230 | |||
| chr2:9919641 | G | T | 7 | a0001 a0002 a0007 others(4): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
missense_variant | MODERATE | c.1386G>T | p.Glu462Asp | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/15 | 1454/2267 | 1386/1767 | 462/588 | chr2 | 9919641 | |||
| chr2:9919715 | C | T | 3 | a0004 a0015 a0016 |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
missense_variant | MODERATE | c.1460C>T | p.Thr487Met | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/15 | 1528/2267 | 1460/1767 | 487/588 | chr2 | 9919715 | |||
| chr2:9933883 | C | A | 2 | a0010 a0014 |
4 | HG00639.hp2 HG02976.hp2 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.1666C>A | p.Leu556Ile | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 15/15 | 1734/2267 | 1666/1767 | 556/588 | chr2 | 9933883 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9868314 | T | C | 2 | a0005c0011 a0011c0010 |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
synonymous_variant | LOW | c.438T>C | p.Ser146Ser | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/15 | 506/2267 | 438/1767 | 146/588 | chr2 | 9868314 | |||
| chr2:9904885 | C | T | 14 | a0001c0001 a0001c0020 a0002c0002 others(11): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
synonymous_variant | LOW | c.834C>T | p.Tyr278Tyr | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/15 | 902/2267 | 834/1767 | 278/588 | chr2 | 9904885 | |||
| chr2:9904984 | C | T | 1 | a0001c0020 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.933C>T | p.Tyr311Tyr | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/15 | 1001/2267 | 933/1767 | 311/588 | chr2 | 9904984 | |||
| chr2:9910749 | C | T | 1 | a0009c0012 | 3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.969C>T | p.Ser323Ser | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/15 | 1037/2267 | 969/1767 | 323/588 | chr2 | 9910749 | |||
| chr2:9910818 | T | C | 7 | a0001c0001 a0001c0020 a0002c0002 others(4): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
synonymous_variant | LOW | c.1038T>C | p.Ala346Ala | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/15 | 1106/2267 | 1038/1767 | 346/588 | chr2 | 9910818 | |||
| chr2:9910842 | C | T | 1 | a0006c0015 | 2 | HG02970.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1062C>T | p.Tyr354Tyr | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/15 | 1130/2267 | 1062/1767 | 354/588 | chr2 | 9910842 | |||
| chr2:9919083 | C | T | 2 | a0005c0011 a0011c0010 |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
synonymous_variant | LOW | c.1314C>T | p.Val438Val | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 13/15 | 1382/2267 | 1314/1767 | 438/588 | chr2 | 9919083 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9843507 | C | T | 1 | a0001c0001t0007 | 1 | HG02738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-35C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/15 | chr2 | 9843507 | |||||||
| chr2:9934000 | A | C | 1 | a0004c0003t0005 | 3 | HG01975.hp1 HG02004.hp1 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 15/15 | 16 | chr2 | 9934000 | ||||||
| chr2:9934078 | G | A | 1 | a0001c0001t0006 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 15/15 | 94 | chr2 | 9934078 | ||||||
| chr2:9934220 | A | G | 1 | a0003c0004t0004 | 4 | NA18984.hp1 NA19010.hp1 NA19065.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*236A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 15/15 | 236 | chr2 | 9934220 | ||||||
| chr2:9934234 | A | G | 1 | a0006c0006t0003 | 5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*250A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 15/15 | 250 | chr2 | 9934234 | ||||||
| chr2:9934255 | G | A | 5 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(2): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*271G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 15/15 | 271 | chr2 | 9934255 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9843575 | A | G | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+16A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843575 | |||||||
| chr2:9843587 | A | C | 337 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(334): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.18+28A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843587 | |||||||
| chr2:9843626 | G | A | 1 | a0004c0003t0001g0032 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.18+67G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843626 | |||||||
| chr2:9843637 | C | A | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.18+78C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843637 | |||||||
| chr2:9843688 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.18+129G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843688 | |||||||
| chr2:9843727 | A | G | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+168A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843727 | |||||||
| chr2:9843831 | C | T | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+272C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843831 | |||||||
| chr2:9843949 | C | A | 1 | a0004c0003t0001g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.18+390C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9843949 | |||||||
| chr2:9844084 | T | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.18+525T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844084 | |||||||
| chr2:9844089 | A | G | 1 | a0001c0001t0002g0345 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.18+530A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844089 | |||||||
| chr2:9844187 | T | G | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+628T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844187 | |||||||
| chr2:9844237 | A | AC | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+678_18+679insC | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844237 | |||||||
| chr2:9844238 | A | C | 11 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(8): Show |
11 | HG01070.hp1 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+679A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844238 | |||||||
| chr2:9844238 | A | T | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.18+679A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844238 | |||||||
| chr2:9844244 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.18+685G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844244 | |||||||
| chr2:9844286 | G | A | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+727G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844286 | |||||||
| chr2:9844316 | AT | A | 8 | a0001c0001t0002g0041 a0002c0002t0001g0039 a0002c0002t0001g0040 others(5): Show |
8 | HG01069.hp1 HG01256.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+770delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 9844316 | ||||||
| chr2:9844330 | A | G | 2 | a0005c0005t0001g0343 a0005c0005t0001g0344 |
2 | NA18940.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.18+771A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844330 | |||||||
| chr2:9844457 | C | T | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-763C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844457 | |||||||
| chr2:9844465 | A | G | 4 | a0003c0004t0001g0342 a0005c0007t0001g0339 a0005c0007t0001g0340 others(1): Show |
4 | HG01496.hp1 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-755A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844465 | |||||||
| chr2:9844469 | G | A | 340 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(337): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.19-751G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844469 | |||||||
| chr2:9844563 | A | G | 1 | a0002c0002t0002g0338 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-657A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844563 | |||||||
| chr2:9844585 | T | G | 27 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(24): Show |
27 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.19-635T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844585 | |||||||
| chr2:9844643 | G | T | 1 | a0010c0014t0001g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.19-577G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844643 | |||||||
| chr2:9844700 | T | C | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-520T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844700 | |||||||
| chr2:9844731 | TC | T | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-485delC | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 9844731 | ||||||
| chr2:9844872 | T | C | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-348T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9844872 | |||||||
| chr2:9845043 | C | T | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-177C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9845043 | |||||||
| chr2:9845051 | T | C | 1 | a0005c0005t0001g0070 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19-169T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9845051 | |||||||
| chr2:9845118 | A | T | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-102A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | chr2 | 9845118 | |||||||
| chr2:9845212 | TC | T | 75 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(72): Show |
75 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(72): Show |
splice_region_variant&intron_variant | LOW | c.19-5delC | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 9845212 | ||||||
| chr2:9845454 | G | A | 1 | a0001c0001t0002g0004 | 2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.117+136G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845454 | |||||||
| chr2:9845472 | A | G | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+154A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845472 | |||||||
| chr2:9845477 | T | C | 47 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0039 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.117+159T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845477 | |||||||
| chr2:9845498 | T | C | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+180T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845498 | |||||||
| chr2:9845541 | T | C | 199 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(196): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.117+223T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845541 | |||||||
| chr2:9845760 | A | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.117+442A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845760 | |||||||
| chr2:9845765 | C | T | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+447C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845765 | |||||||
| chr2:9845828 | C | A | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+510C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845828 | |||||||
| chr2:9845877 | A | G | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+559A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845877 | |||||||
| chr2:9845914 | C | T | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+596C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845914 | |||||||
| chr2:9845925 | G | T | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+607G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845925 | |||||||
| chr2:9845931 | C | T | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+613C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845931 | |||||||
| chr2:9845939 | C | T | 3 | a0005c0005t0001g0013 a0006c0006t0003g0001 a0006c0006t0003g0012 |
6 | HG01109.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+621C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845939 | |||||||
| chr2:9845947 | T | C | 1 | a0006c0006t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.117+629T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845947 | |||||||
| chr2:9845954 | G | T | 1 | a0005c0005t0001g0110 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.117+636G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9845954 | |||||||
| chr2:9845973 | ACT | A | 39 | a0005c0005t0001g0070 a0005c0005t0001g0075 a0005c0005t0001g0076 others(36): Show |
39 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.117+658_117+659del others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 9845973 | ||||||
| chr2:9846033 | C | T | 42 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0039 others(39): Show |
42 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.117+715C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9846033 | |||||||
| chr2:9846034 | G | A | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+716G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9846034 | |||||||
| chr2:9846087 | A | G | 1 | a0004c0003t0001g0332 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.117+769A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9846087 | |||||||
| chr2:9846348 | G | A | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+1030G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9846348 | |||||||
| chr2:9846604 | T | C | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+1286T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9846604 | |||||||
| chr2:9846740 | T | C | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.117+1422T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9846740 | |||||||
| chr2:9846842 | GTGTGTGT others(3): Show |
G | 2 | a0005c0005t0001g0075 a0005c0005t0001g0076 |
2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.117+1535_117+1544d others(12): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 9846842 | ||||||
| chr2:9847061 | A | G | 81 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(78): Show |
81 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.117+1743A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847061 | |||||||
| chr2:9847245 | A | G | 1 | a0010c0014t0001g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.117+1927A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847245 | |||||||
| chr2:9847252 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.117+1934C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847252 | |||||||
| chr2:9847380 | G | A | 9 | a0002c0002t0001g0116 a0002c0002t0001g0355 a0002c0002t0001g0356 others(6): Show |
9 | HG00099.hp1 HG01168.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-1993G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847380 | |||||||
| chr2:9847390 | T | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1983T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847390 | |||||||
| chr2:9847396 | A | T | 9 | a0002c0002t0001g0116 a0002c0002t0001g0355 a0002c0002t0001g0356 others(6): Show |
9 | HG00099.hp1 HG01168.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-1977A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847396 | |||||||
| chr2:9847414 | A | G | 1 | a0002c0002t0001g0069 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.118-1959A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847414 | |||||||
| chr2:9847525 | C | T | 1 | a0001c0001t0002g0331 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118-1848C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847525 | |||||||
| chr2:9847533 | G | A | 1 | a0002c0002t0001g0355 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118-1840G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847533 | |||||||
| chr2:9847546 | T | C | 78 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(75): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.118-1827T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847546 | |||||||
| chr2:9847558 | G | A | 1 | a0002c0002t0002g0117 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.118-1815G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847558 | |||||||
| chr2:9847573 | C | T | 7 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0065 others(4): Show |
7 | HG00609.hp1 NA18943.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-1800C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847573 | |||||||
| chr2:9847581 | A | G | 6 | a0001c0001t0002g0003 a0001c0001t0002g0208 a0001c0001t0002g0209 others(3): Show |
8 | NA18945.hp2 NA18954.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-1792A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847581 | |||||||
| chr2:9847591 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.118-1782A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847591 | |||||||
| chr2:9847655 | AT | A | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.118-1717delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847655 | |||||||
| chr2:9847692 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.118-1681T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847692 | |||||||
| chr2:9847799 | T | A | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-1574T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847799 | |||||||
| chr2:9847829 | A | G | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.118-1544A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9847829 | |||||||
| chr2:9847852 | CTT | C | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.118-1516_118-1515d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 9847852 | ||||||
| chr2:9848000 | A | G | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.118-1373A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848000 | |||||||
| chr2:9848170 | T | C | 67 | a0001c0001t0001g0261 a0003c0004t0001g0253 a0003c0004t0001g0260 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.118-1203T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848170 | |||||||
| chr2:9848198 | T | C | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.118-1175T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848198 | |||||||
| chr2:9848219 | T | G | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.118-1154T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848219 | |||||||
| chr2:9848229 | A | G | 5 | a0005c0005t0001g0105 a0005c0005t0001g0106 a0005c0005t0001g0107 others(2): Show |
5 | HG02027.hp2 NA18612.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-1144A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848229 | |||||||
| chr2:9848230 | C | T | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.118-1143C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848230 | |||||||
| chr2:9848442 | A | G | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.118-931A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848442 | |||||||
| chr2:9848532 | G | C | 18 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(15): Show |
21 | HG00280.hp2 HG02040.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.118-841G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848532 | |||||||
| chr2:9848537 | A | G | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.118-836A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848537 | |||||||
| chr2:9848603 | T | G | 1 | a0003c0004t0001g0276 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.118-770T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848603 | |||||||
| chr2:9848610 | G | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.118-763G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848610 | |||||||
| chr2:9848620 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.118-753C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848620 | |||||||
| chr2:9848621 | G | T | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.118-752G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848621 | |||||||
| chr2:9848666 | C | CAA | 79 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(76): Show |
88 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.118-697_118-696dup others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 9848666 | ||||||
| chr2:9848684 | G | T | 13 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(10): Show |
13 | HG00323.hp1 HG01106.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.118-689G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848684 | |||||||
| chr2:9848686 | C | G | 1 | a0002c0002t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.118-687C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848686 | |||||||
| chr2:9848700 | C | T | 1 | a0005c0005t0001g0070 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.118-673C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848700 | |||||||
| chr2:9848774 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.118-599G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848774 | |||||||
| chr2:9848858 | T | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-515T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848858 | |||||||
| chr2:9848950 | A | T | 1 | a0001c0001t0002g0204 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.118-423A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9848950 | |||||||
| chr2:9849047 | G | A | 27 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(24): Show |
27 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.118-326G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9849047 | |||||||
| chr2:9849313 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.118-60A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 2/14 | chr2 | 9849313 | |||||||
| chr2:9849573 | A | G | 1 | a0003c0004t0004g0329 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.205+113A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849573 | |||||||
| chr2:9849574 | T | C | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.205+114T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849574 | |||||||
| chr2:9849633 | T | C | 356 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(353): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.205+173T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849633 | |||||||
| chr2:9849634 | G | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.205+174G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849634 | |||||||
| chr2:9849646 | G | C | 1 | a0004c0003t0001g0042 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.205+186G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849646 | |||||||
| chr2:9849822 | G | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.205+362G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849822 | |||||||
| chr2:9849853 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.205+393A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849853 | |||||||
| chr2:9849939 | C | T | 1 | a0006c0006t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.205+479C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849939 | |||||||
| chr2:9849954 | G | A | 4 | a0004c0003t0001g0216 a0004c0003t0001g0217 a0004c0003t0001g0218 others(1): Show |
4 | HG02080.hp2 NA18970.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.205+494G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9849954 | |||||||
| chr2:9850014 | A | AAT | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.205+567_205+568dup others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 9850014 | ||||||
| chr2:9850014 | AAT | A | 46 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(43): Show |
46 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.205+567_205+568del others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 9850014 | ||||||
| chr2:9850016 | T | A | 1 | a0004c0003t0001g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.205+556T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850016 | |||||||
| chr2:9850025 | ATATGTGT others(3): Show |
A | 67 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(64): Show |
76 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.205+567_205+576del others(10): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 9850025 | ||||||
| chr2:9850027 | A | ATG | 13 | a0005c0005t0001g0033 a0005c0007t0001g0011 a0005c0007t0001g0333 others(10): Show |
17 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.205+595_205+596dup others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 9850027 | ||||||
| chr2:9850027 | A | G | 3 | a0001c0001t0002g0041 a0002c0002t0001g0141 a0002c0002t0001g0142 |
3 | HG01257.hp1 HG03942.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.205+567A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850027 | |||||||
| chr2:9850027 | ATG | A | 32 | a0002c0002t0001g0111 a0002c0002t0001g0112 a0002c0002t0001g0113 others(29): Show |
32 | HG00438.hp1 HG01256.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.205+595_205+596del others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 9850027 | ||||||
| chr2:9850027 | ATGTG | A | 126 | a0001c0001t0001g0261 a0003c0004t0001g0010 a0003c0004t0001g0044 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.205+593_205+596del others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 9850027 | ||||||
| chr2:9850027 | ATGTGTG | A | 38 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(35): Show |
38 | HG00597.hp1 HG00609.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.205+591_205+596del others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 9850027 | ||||||
| chr2:9850031 | G | A | 1 | a0003c0004t0001g0292 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.205+571G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850031 | |||||||
| chr2:9850079 | C | T | 2 | a0003c0004t0001g0327 a0003c0004t0001g0328 |
2 | HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.205+619C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850079 | |||||||
| chr2:9850080 | G | A | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.205+620G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850080 | |||||||
| chr2:9850152 | T | C | 2 | a0003c0004t0001g0327 a0003c0004t0001g0328 |
2 | HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.205+692T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850152 | |||||||
| chr2:9850296 | A | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+836A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850296 | |||||||
| chr2:9850304 | A | G | 6 | a0005c0005t0001g0104 a0005c0005t0001g0105 a0005c0005t0001g0106 others(3): Show |
6 | HG02027.hp2 NA18612.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+844A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850304 | |||||||
| chr2:9850400 | T | C | 1 | a0005c0005t0001g0077 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.205+940T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850400 | |||||||
| chr2:9850662 | G | A | 3 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 |
3 | HG01070.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.206-879G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850662 | |||||||
| chr2:9850956 | G | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.206-585G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9850956 | |||||||
| chr2:9851194 | C | G | 1 | a0002c0002t0001g0062 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.206-347C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9851194 | |||||||
| chr2:9851398 | A | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.206-143A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9851398 | |||||||
| chr2:9851427 | G | A | 356 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(353): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.206-114G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9851427 | |||||||
| chr2:9851451 | G | A | 1 | a0005c0007t0001g0333 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-90G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 3/14 | chr2 | 9851451 | |||||||
| chr2:9851738 | G | A | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.303+100G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9851738 | |||||||
| chr2:9851944 | T | C | 1 | a0014c0017t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.303+306T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9851944 | |||||||
| chr2:9852075 | G | T | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+437G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852075 | |||||||
| chr2:9852111 | C | T | 1 | a0002c0002t0001g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.303+473C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852111 | |||||||
| chr2:9852180 | G | A | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.303+542G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852180 | |||||||
| chr2:9852496 | A | ATT | 77 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(74): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.303+868_303+869dup others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 9852496 | ||||||
| chr2:9852522 | C | T | 1 | a0002c0002t0001g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.303+884C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852522 | |||||||
| chr2:9852653 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.303+1015A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852653 | |||||||
| chr2:9852743 | C | T | 2 | a0003c0004t0001g0325 a0003c0004t0001g0326 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.303+1105C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852743 | |||||||
| chr2:9852781 | A | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+1143A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852781 | |||||||
| chr2:9852926 | A | G | 14 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(11): Show |
14 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.303+1288A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852926 | |||||||
| chr2:9852972 | G | A | 1 | a0003c0004t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.303+1334G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9852972 | |||||||
| chr2:9853058 | G | T | 8 | a0003c0004t0001g0276 a0003c0004t0001g0318 a0003c0004t0001g0319 others(5): Show |
8 | HG02280.hp1 HG02572.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.304-1268G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853058 | |||||||
| chr2:9853228 | A | AT | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.304-1097dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 9853228 | ||||||
| chr2:9853254 | G | A | 3 | a0005c0007t0001g0339 a0005c0007t0001g0340 a0005c0007t0001g0341 |
3 | HG01496.hp1 HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.304-1072G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853254 | |||||||
| chr2:9853322 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.304-1004G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853322 | |||||||
| chr2:9853490 | C | T | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG02145.hp2 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.304-836C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853490 | |||||||
| chr2:9853655 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.304-671A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853655 | |||||||
| chr2:9853668 | A | T | 1 | a0004c0003t0001g0332 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.304-658A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853668 | |||||||
| chr2:9853841 | G | A | 1 | a0002c0002t0001g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.304-485G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853841 | |||||||
| chr2:9853884 | T | G | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-442T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853884 | |||||||
| chr2:9853912 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.304-414C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853912 | |||||||
| chr2:9853961 | G | C | 71 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(68): Show |
80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.304-365G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9853961 | |||||||
| chr2:9854002 | T | C | 2 | a0004c0003t0001g0220 a0004c0003t0001g0221 |
2 | NA18965.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.304-324T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9854002 | |||||||
| chr2:9854159 | C | G | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.304-167C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9854159 | |||||||
| chr2:9854163 | C | T | 1 | a0002c0002t0001g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.304-163C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9854163 | |||||||
| chr2:9854164 | C | T | 27 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(24): Show |
27 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.304-162C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 4/14 | chr2 | 9854164 | |||||||
| chr2:9854443 | T | C | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+22T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854443 | |||||||
| chr2:9854588 | C | T | 39 | a0005c0005t0001g0013 a0005c0005t0001g0070 a0005c0005t0001g0075 others(36): Show |
39 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.399+167C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854588 | |||||||
| chr2:9854665 | CAT | C | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.399+246_399+247del others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9854665 | ||||||
| chr2:9854769 | A | C | 1 | a0003c0004t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.399+348A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854769 | |||||||
| chr2:9854815 | A | G | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+394A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854815 | |||||||
| chr2:9854942 | C | T | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.399+521C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854942 | |||||||
| chr2:9854975 | T | A | 1 | a0003c0004t0001g0278 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.399+554T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854975 | |||||||
| chr2:9854981 | T | A | 1 | a0003c0004t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.399+560T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854981 | |||||||
| chr2:9854997 | G | T | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.399+576G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9854997 | |||||||
| chr2:9855002 | GT | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+590delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9855002 | ||||||
| chr2:9855143 | C | T | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.399+722C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9855143 | |||||||
| chr2:9855276 | T | G | 1 | a0002c0002t0001g0063 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.399+855T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9855276 | |||||||
| chr2:9855287 | G | A | 1 | a0002c0002t0001g0064 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.399+866G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9855287 | |||||||
| chr2:9855542 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+1121A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9855542 | |||||||
| chr2:9855852 | ATTACT | A | 5 | a0002c0002t0001g0116 a0002c0002t0001g0119 a0002c0002t0001g0120 others(2): Show |
5 | HG00642.hp1 HG00733.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+1437_399+1441d others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9855852 | ||||||
| chr2:9855986 | A | G | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | NA18941.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.399+1565A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9855986 | |||||||
| chr2:9856027 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+1606T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856027 | |||||||
| chr2:9856234 | C | T | 1 | a0003c0004t0001g0328 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.399+1813C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856234 | |||||||
| chr2:9856235 | G | A | 1 | a0012c0013t0001g0045 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.399+1814G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856235 | |||||||
| chr2:9856238 | C | T | 4 | a0003c0004t0004g0315 a0003c0004t0004g0316 a0003c0004t0004g0329 others(1): Show |
4 | NA18984.hp2 NA19010.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+1817C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856238 | |||||||
| chr2:9856261 | A | G | 1 | a0005c0005t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.399+1840A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856261 | |||||||
| chr2:9856366 | A | G | 2 | a0004c0003t0001g0274 a0004c0003t0001g0275 |
2 | NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.399+1945A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856366 | |||||||
| chr2:9856443 | A | G | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+2022A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856443 | |||||||
| chr2:9856470 | G | A | 2 | a0004c0003t0001g0222 a0004c0003t0001g0223 |
2 | NA18971.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.399+2049G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856470 | |||||||
| chr2:9856494 | C | T | 66 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(63): Show |
66 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.399+2073C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856494 | |||||||
| chr2:9856523 | A | G | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+2102A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856523 | |||||||
| chr2:9856554 | A | T | 46 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(43): Show |
46 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.399+2133A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856554 | |||||||
| chr2:9856673 | T | C | 2 | a0004c0003t0001g0224 a0004c0003t0001g0225 |
2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.399+2252T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856673 | |||||||
| chr2:9856693 | T | A | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.399+2272T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856693 | |||||||
| chr2:9856739 | C | T | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+2318C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856739 | |||||||
| chr2:9856758 | A | G | 2 | a0005c0007t0001g0073 a0014c0017t0001g0071 |
2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.399+2337A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856758 | |||||||
| chr2:9856924 | T | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+2503T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856924 | |||||||
| chr2:9856983 | C | T | 1 | a0010c0014t0001g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.399+2562C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9856983 | |||||||
| chr2:9857409 | G | A | 1 | a0004c0003t0001g0226 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.399+2988G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857409 | |||||||
| chr2:9857493 | G | A | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.399+3072G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857493 | |||||||
| chr2:9857507 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.399+3086G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857507 | |||||||
| chr2:9857526 | T | C | 53 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(50): Show |
56 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.399+3105T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857526 | |||||||
| chr2:9857562 | A | T | 4 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+3141A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857562 | |||||||
| chr2:9857627 | G | A | 3 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 |
3 | HG01070.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.399+3206G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857627 | |||||||
| chr2:9857634 | TA | T | 4 | a0008c0009t0001g0038 a0008c0009t0001g0053 a0008c0009t0001g0054 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+3215delA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9857634 | ||||||
| chr2:9857665 | A | G | 76 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(73): Show |
76 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.399+3244A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857665 | |||||||
| chr2:9857760 | C | G | 160 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(157): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.399+3339C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857760 | |||||||
| chr2:9857815 | C | T | 1 | a0004c0003t0001g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.399+3394C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857815 | |||||||
| chr2:9857877 | C | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.399+3456C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9857877 | |||||||
| chr2:9858039 | C | T | 46 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(43): Show |
46 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.399+3618C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858039 | |||||||
| chr2:9858205 | T | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.399+3784T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858205 | |||||||
| chr2:9858209 | C | G | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+3788C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858209 | |||||||
| chr2:9858309 | G | A | 3 | a0011c0010t0001g0352 a0011c0010t0001g0353 a0011c0010t0001g0354 |
3 | HG01109.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.399+3888G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858309 | |||||||
| chr2:9858318 | A | G | 5 | a0005c0007t0001g0052 a0005c0007t0001g0056 a0005c0007t0001g0057 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+3897A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858318 | |||||||
| chr2:9858400 | G | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+3979G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858400 | |||||||
| chr2:9858532 | C | T | 5 | a0005c0007t0001g0073 a0010c0014t0001g0072 a0010c0014t0001g0074 others(2): Show |
5 | HG00639.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+4111C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858532 | |||||||
| chr2:9858587 | G | T | 1 | a0001c0001t0002g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.399+4166G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858587 | |||||||
| chr2:9858676 | C | G | 3 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 |
3 | HG01070.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.399+4255C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858676 | |||||||
| chr2:9858681 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.399+4260A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858681 | |||||||
| chr2:9858687 | C | T | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.399+4266C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858687 | |||||||
| chr2:9858699 | C | T | 4 | a0004c0003t0001g0273 a0005c0007t0001g0339 a0005c0007t0001g0340 others(1): Show |
4 | HG01496.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+4278C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858699 | |||||||
| chr2:9858700 | G | A | 3 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0020t0002g0169 |
3 | HG00735.hp1 HG00738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.399+4279G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858700 | |||||||
| chr2:9858715 | C | G | 39 | a0005c0005t0001g0013 a0005c0005t0001g0070 a0005c0005t0001g0075 others(36): Show |
39 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.399+4294C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858715 | |||||||
| chr2:9858753 | G | C | 1 | a0003c0004t0001g0280 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.399+4332G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858753 | |||||||
| chr2:9858790 | T | G | 1 | a0004c0003t0001g0227 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.399+4369T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858790 | |||||||
| chr2:9858812 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.399+4391G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858812 | |||||||
| chr2:9858825 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.399+4404G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858825 | |||||||
| chr2:9858838 | A | G | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.399+4417A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858838 | |||||||
| chr2:9858859 | G | A | 70 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(67): Show |
79 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.399+4438G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858859 | |||||||
| chr2:9858907 | C | T | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.399+4486C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858907 | |||||||
| chr2:9858913 | C | T | 1 | a0002c0002t0001g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.399+4492C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9858913 | |||||||
| chr2:9859050 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.399+4629C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859050 | |||||||
| chr2:9859054 | C | T | 6 | a0004c0003t0001g0220 a0004c0003t0001g0221 a0004c0003t0001g0269 others(3): Show |
6 | HG02083.hp2 NA18965.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+4633C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859054 | |||||||
| chr2:9859196 | T | TTTC | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.399+4777_399+4779d others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9859196 | ||||||
| chr2:9859228 | G | A | 340 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(337): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.399+4807G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859228 | |||||||
| chr2:9859386 | A | AT | 31 | a0002c0002t0001g0137 a0003c0004t0001g0276 a0003c0004t0001g0319 others(28): Show |
31 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+4983dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9859386 | ||||||
| chr2:9859386 | A | ATTT | 47 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0002g0003 others(44): Show |
53 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.399+4981_399+4983d others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9859386 | ||||||
| chr2:9859386 | A | ATTTT | 17 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0202 others(14): Show |
20 | HG01123.hp2 HG02040.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.399+4980_399+4983d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9859386 | ||||||
| chr2:9859386 | AT | A | 55 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(52): Show |
55 | HG00597.hp1 HG00609.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.399+4983delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9859386 | ||||||
| chr2:9859428 | G | A | 1 | a0006c0006t0001g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.399+5007G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859428 | |||||||
| chr2:9859489 | C | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+5068C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859489 | |||||||
| chr2:9859623 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+5202G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859623 | |||||||
| chr2:9859693 | G | A | 4 | a0005c0005t0001g0033 a0005c0007t0001g0339 a0005c0007t0001g0340 others(1): Show |
4 | HG01496.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+5272G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859693 | |||||||
| chr2:9859756 | T | G | 2 | a0007c0008t0001g0229 a0007c0008t0001g0230 |
2 | NA18946.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.399+5335T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9859756 | |||||||
| chr2:9860017 | G | A | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+5596G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860017 | |||||||
| chr2:9860051 | T | C | 16 | a0003c0004t0001g0280 a0003c0004t0001g0281 a0003c0004t0001g0282 others(13): Show |
16 | HG01123.hp1 HG01516.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.399+5630T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860051 | |||||||
| chr2:9860303 | C | T | 1 | a0006c0006t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+5882C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860303 | |||||||
| chr2:9860358 | G | T | 1 | a0004c0003t0001g0262 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.399+5937G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860358 | |||||||
| chr2:9860376 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.399+5955C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860376 | |||||||
| chr2:9860573 | G | A | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.399+6152G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860573 | |||||||
| chr2:9860797 | G | C | 22 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(19): Show |
22 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.399+6376G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860797 | |||||||
| chr2:9860826 | T | C | 1 | a0005c0005t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.399+6405T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860826 | |||||||
| chr2:9860866 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+6445A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9860866 | |||||||
| chr2:9861023 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.399+6602G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861023 | |||||||
| chr2:9861257 | C | T | 1 | a0011c0010t0001g0354 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.399+6836C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861257 | |||||||
| chr2:9861258 | G | A | 4 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(1): Show |
4 | HG02027.hp2 HG02145.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+6837G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861258 | |||||||
| chr2:9861307 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.399+6886A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861307 | |||||||
| chr2:9861341 | C | T | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+6920C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861341 | |||||||
| chr2:9861417 | C | A | 1 | a0003c0004t0001g0280 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.400-6859C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861417 | |||||||
| chr2:9861610 | C | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-6666C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861610 | |||||||
| chr2:9861696 | C | G | 1 | a0001c0001t0001g0261 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.400-6580C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861696 | |||||||
| chr2:9861723 | G | A | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-6553G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861723 | |||||||
| chr2:9861760 | C | T | 1 | a0006c0006t0001g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.400-6516C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861760 | |||||||
| chr2:9861865 | A | G | 8 | a0005c0007t0001g0073 a0005c0007t0001g0339 a0005c0007t0001g0340 others(5): Show |
8 | HG00639.hp2 HG01496.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-6411A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861865 | |||||||
| chr2:9861910 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-6366A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9861910 | |||||||
| chr2:9862036 | C | T | 83 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(80): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.400-6240C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862036 | |||||||
| chr2:9862040 | TCTC | T | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.400-6231_400-6229d others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9862040 | ||||||
| chr2:9862171 | T | C | 1 | a0010c0014t0001g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.400-6105T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862171 | |||||||
| chr2:9862241 | A | G | 5 | a0005c0007t0001g0073 a0010c0014t0001g0072 a0010c0014t0001g0074 others(2): Show |
5 | HG00639.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-6035A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862241 | |||||||
| chr2:9862315 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-5961T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862315 | |||||||
| chr2:9862430 | A | G | 27 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(24): Show |
27 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.400-5846A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862430 | |||||||
| chr2:9862554 | G | C | 1 | a0003c0016t0001g0207 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.400-5722G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862554 | |||||||
| chr2:9862612 | C | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-5664C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862612 | |||||||
| chr2:9862663 | T | C | 2 | a0005c0007t0001g0073 a0014c0017t0001g0071 |
2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.400-5613T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862663 | |||||||
| chr2:9862685 | A | T | 2 | a0005c0005t0001g0343 a0005c0005t0001g0344 |
2 | NA18940.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.400-5591A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862685 | |||||||
| chr2:9862703 | G | A | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.400-5573G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862703 | |||||||
| chr2:9862764 | G | A | 5 | a0002c0002t0001g0116 a0002c0002t0001g0119 a0002c0002t0001g0120 others(2): Show |
5 | HG00642.hp1 HG00733.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-5512G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862764 | |||||||
| chr2:9862776 | T | G | 1 | a0004c0003t0001g0263 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.400-5500T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862776 | |||||||
| chr2:9862904 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.400-5372T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862904 | |||||||
| chr2:9862963 | A | G | 1 | a0005c0005t0001g0102 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.400-5313A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862963 | |||||||
| chr2:9862973 | C | T | 1 | a0005c0005t0001g0102 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.400-5303C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862973 | |||||||
| chr2:9862979 | A | G | 1 | a0005c0005t0001g0102 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.400-5297A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9862979 | |||||||
| chr2:9863079 | C | G | 1 | a0001c0001t0002g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.400-5197C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9863079 | |||||||
| chr2:9863115 | A | C | 1 | a0003c0004t0004g0315 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.400-5161A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9863115 | |||||||
| chr2:9863209 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.400-5067A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9863209 | |||||||
| chr2:9863452 | C | T | 1 | a0003c0004t0001g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.400-4824C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9863452 | |||||||
| chr2:9863624 | C | T | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.400-4652C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9863624 | |||||||
| chr2:9863710 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-4566T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9863710 | |||||||
| chr2:9863798 | C | G | 52 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(49): Show |
52 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.400-4478C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9863798 | |||||||
| chr2:9864079 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-4197A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864079 | |||||||
| chr2:9864284 | G | GAAATACA others(2): Show |
82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-3992_400-3991i others(11): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864284 | |||||||
| chr2:9864331 | G | A | 158 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(155): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.400-3945G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864331 | |||||||
| chr2:9864359 | G | A | 11 | a0003c0004t0001g0260 a0004c0003t0001g0216 a0004c0003t0001g0217 others(8): Show |
11 | HG00741.hp2 HG02080.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.400-3917G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864359 | |||||||
| chr2:9864381 | T | C | 2 | a0004c0003t0001g0216 a0004c0003t0001g0217 |
2 | NA19011.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.400-3895T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864381 | |||||||
| chr2:9864508 | G | A | 27 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(24): Show |
27 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.400-3768G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864508 | |||||||
| chr2:9864706 | C | T | 1 | a0014c0017t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.400-3570C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864706 | |||||||
| chr2:9864789 | A | G | 340 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(337): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.400-3487A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864789 | |||||||
| chr2:9864898 | G | C | 1 | a0001c0001t0002g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400-3378G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864898 | |||||||
| chr2:9864917 | T | G | 1 | a0004c0003t0001g0231 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.400-3359T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864917 | |||||||
| chr2:9864969 | C | T | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.400-3307C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9864969 | |||||||
| chr2:9865048 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0215 |
2 | HG00738.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.400-3228C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865048 | |||||||
| chr2:9865052 | C | T | 1 | a0005c0005t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.400-3224C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865052 | |||||||
| chr2:9865063 | G | C | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | NA18964.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.400-3213G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865063 | |||||||
| chr2:9865126 | A | G | 127 | a0001c0001t0001g0261 a0003c0004t0001g0010 a0003c0004t0001g0044 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.400-3150A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865126 | |||||||
| chr2:9865175 | A | G | 160 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(157): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.400-3101A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865175 | |||||||
| chr2:9865195 | T | C | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.400-3081T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865195 | |||||||
| chr2:9865196 | G | A | 1 | a0003c0004t0001g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.400-3080G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865196 | |||||||
| chr2:9865205 | C | G | 1 | a0003c0016t0001g0259 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.400-3071C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865205 | |||||||
| chr2:9865255 | A | G | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-3021A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865255 | |||||||
| chr2:9865319 | A | T | 1 | a0012c0013t0001g0051 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.400-2957A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865319 | |||||||
| chr2:9865338 | C | T | 1 | a0004c0003t0001g0042 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.400-2938C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865338 | |||||||
| chr2:9865495 | C | T | 1 | a0005c0005t0001g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.400-2781C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865495 | |||||||
| chr2:9865496 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-2780G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865496 | |||||||
| chr2:9865540 | T | C | 1 | a0004c0003t0001g0264 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.400-2736T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865540 | |||||||
| chr2:9865611 | C | T | 16 | a0003c0004t0001g0302 a0003c0004t0001g0303 a0003c0004t0001g0304 others(13): Show |
16 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.400-2665C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865611 | |||||||
| chr2:9865667 | G | A | 1 | a0004c0003t0001g0218 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.400-2609G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865667 | |||||||
| chr2:9865691 | C | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.400-2585C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865691 | |||||||
| chr2:9865741 | C | T | 356 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(353): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.400-2535C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865741 | |||||||
| chr2:9865826 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.400-2450G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865826 | |||||||
| chr2:9865827 | C | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-2449C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865827 | |||||||
| chr2:9865830 | A | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-2446A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9865830 | |||||||
| chr2:9866064 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-2212A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866064 | |||||||
| chr2:9866078 | T | A | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.400-2198T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866078 | |||||||
| chr2:9866090 | T | C | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.400-2186T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866090 | |||||||
| chr2:9866104 | A | C | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.400-2172A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866104 | |||||||
| chr2:9866105 | G | A | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.400-2171G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866105 | |||||||
| chr2:9866108 | C | T | 3 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 |
3 | HG01070.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.400-2168C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866108 | |||||||
| chr2:9866205 | T | C | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.400-2071T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866205 | |||||||
| chr2:9866211 | A | G | 4 | a0003c0004t0001g0044 a0003c0004t0001g0299 a0003c0004t0001g0300 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-2065A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866211 | |||||||
| chr2:9866290 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-1986T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866290 | |||||||
| chr2:9866341 | A | G | 1 | a0002c0002t0001g0355 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.400-1935A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866341 | |||||||
| chr2:9866398 | G | A | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.400-1878G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866398 | |||||||
| chr2:9866413 | G | A | 75 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(72): Show |
75 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.400-1863G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866413 | |||||||
| chr2:9866441 | T | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.400-1835T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866441 | |||||||
| chr2:9866642 | G | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-1634G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866642 | |||||||
| chr2:9866642 | G | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.400-1634G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866642 | |||||||
| chr2:9866877 | A | G | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG02145.hp2 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.400-1399A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866877 | |||||||
| chr2:9866921 | T | C | 157 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(154): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.400-1355T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866921 | |||||||
| chr2:9866950 | G | A | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.400-1326G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866950 | |||||||
| chr2:9866959 | A | G | 1 | a0002c0002t0001g0063 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.400-1317A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9866959 | |||||||
| chr2:9867121 | G | C | 1 | a0001c0001t0002g0174 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.400-1155G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867121 | |||||||
| chr2:9867270 | A | G | 1 | a0006c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.400-1006A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867270 | |||||||
| chr2:9867455 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.400-821A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867455 | |||||||
| chr2:9867461 | C | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.400-815C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867461 | |||||||
| chr2:9867527 | A | C | 1 | a0001c0001t0002g0167 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.400-749A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867527 | |||||||
| chr2:9867549 | G | A | 1 | a0004c0003t0001g0232 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.400-727G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867549 | |||||||
| chr2:9867602 | T | C | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(44): Show |
47 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.400-674T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867602 | |||||||
| chr2:9867662 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.400-614C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867662 | |||||||
| chr2:9867687 | ACT | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.400-586_400-585del others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 9867687 | ||||||
| chr2:9867694 | T | C | 287 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(284): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.400-582T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867694 | |||||||
| chr2:9867715 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.400-561A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867715 | |||||||
| chr2:9867817 | G | A | 1 | a0003c0004t0001g0281 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.400-459G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867817 | |||||||
| chr2:9867849 | A | C | 1 | a0003c0004t0001g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.400-427A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867849 | |||||||
| chr2:9867988 | A | T | 1 | a0002c0002t0001g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.400-288A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9867988 | |||||||
| chr2:9868069 | G | A | 3 | a0005c0007t0001g0339 a0005c0007t0001g0340 a0005c0007t0001g0341 |
3 | HG01496.hp1 HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.400-207G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 5/14 | chr2 | 9868069 | |||||||
| chr2:9868663 | G | A | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.553+234G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9868663 | |||||||
| chr2:9868732 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.553+303C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9868732 | |||||||
| chr2:9868733 | G | A | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.553+304G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9868733 | |||||||
| chr2:9868743 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+314A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9868743 | |||||||
| chr2:9868873 | C | T | 1 | a0005c0007t0001g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.553+444C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9868873 | |||||||
| chr2:9868903 | A | G | 2 | a0005c0011t0001g0350 a0005c0011t0001g0351 |
2 | HG01070.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.553+474A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9868903 | |||||||
| chr2:9869062 | T | A | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.553+633T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869062 | |||||||
| chr2:9869063 | C | T | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.553+634C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869063 | |||||||
| chr2:9869217 | T | G | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.553+788T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869217 | |||||||
| chr2:9869245 | G | A | 1 | a0005c0005t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.553+816G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869245 | |||||||
| chr2:9869469 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+1040T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869469 | |||||||
| chr2:9869472 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+1043T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869472 | |||||||
| chr2:9869601 | C | T | 2 | a0004c0003t0001g0258 a0004c0003t0001g0264 |
2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.553+1172C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869601 | |||||||
| chr2:9869641 | T | G | 3 | a0004c0003t0005g0233 a0004c0003t0005g0234 a0004c0003t0005g0235 |
3 | HG01975.hp1 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.553+1212T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869641 | |||||||
| chr2:9869756 | G | C | 39 | a0005c0005t0001g0013 a0005c0005t0001g0070 a0005c0005t0001g0075 others(36): Show |
39 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.553+1327G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869756 | |||||||
| chr2:9869758 | C | T | 39 | a0005c0005t0001g0013 a0005c0005t0001g0070 a0005c0005t0001g0075 others(36): Show |
39 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.553+1329C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869758 | |||||||
| chr2:9869821 | A | G | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.553+1392A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869821 | |||||||
| chr2:9869966 | C | T | 1 | a0002c0002t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.553+1537C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869966 | |||||||
| chr2:9869978 | G | A | 124 | a0001c0001t0001g0261 a0003c0004t0001g0010 a0003c0004t0001g0044 others(121): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.553+1549G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869978 | |||||||
| chr2:9869990 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.553+1561G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9869990 | |||||||
| chr2:9870028 | C | T | 2 | a0002c0002t0002g0136 a0004c0003t0001g0263 |
2 | HG02273.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.553+1599C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870028 | |||||||
| chr2:9870106 | T | TAATA | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+1685_553+1688d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 9870106 | ||||||
| chr2:9870130 | A | G | 8 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(5): Show |
8 | HG00099.hp1 HG01168.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.553+1701A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870130 | |||||||
| chr2:9870171 | T | C | 335 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.553+1742T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870171 | |||||||
| chr2:9870202 | C | T | 124 | a0001c0001t0001g0261 a0003c0004t0001g0010 a0003c0004t0001g0044 others(121): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.553+1773C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870202 | |||||||
| chr2:9870231 | T | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.553+1802T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870231 | |||||||
| chr2:9870286 | C | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+1857C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870286 | |||||||
| chr2:9870366 | C | T | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.553+1937C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870366 | |||||||
| chr2:9870437 | T | C | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.553+2008T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870437 | |||||||
| chr2:9870461 | C | T | 337 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(334): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.553+2032C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870461 | |||||||
| chr2:9870469 | G | A | 39 | a0005c0005t0001g0013 a0005c0005t0001g0070 a0005c0005t0001g0075 others(36): Show |
39 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.553+2040G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870469 | |||||||
| chr2:9870639 | T | C | 157 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(154): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.553+2210T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870639 | |||||||
| chr2:9870640 | G | A | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.553+2211G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870640 | |||||||
| chr2:9870721 | CTCTT | C | 3 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 |
3 | HG01070.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.553+2293_553+2296d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870721 | |||||||
| chr2:9870820 | T | TA | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.553+2392dupA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 9870820 | ||||||
| chr2:9870946 | T | C | 48 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(45): Show |
48 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.553+2517T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9870946 | |||||||
| chr2:9871105 | T | A | 334 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(331): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.553+2676T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871105 | |||||||
| chr2:9871105 | T | G | 3 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 |
3 | HG01070.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.553+2676T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871105 | |||||||
| chr2:9871205 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.553+2776G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871205 | |||||||
| chr2:9871236 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+2807T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871236 | |||||||
| chr2:9871356 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.553+2927G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871356 | |||||||
| chr2:9871488 | G | A | 38 | a0005c0005t0001g0013 a0005c0005t0001g0070 a0005c0005t0001g0075 others(35): Show |
38 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.553+3059G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871488 | |||||||
| chr2:9871618 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.553+3189A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871618 | |||||||
| chr2:9871757 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+3328T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871757 | |||||||
| chr2:9871843 | C | T | 52 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(49): Show |
52 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.553+3414C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871843 | |||||||
| chr2:9871890 | C | T | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.553+3461C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871890 | |||||||
| chr2:9871898 | T | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.553+3469T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871898 | |||||||
| chr2:9871898 | T | G | 79 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(76): Show |
88 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.553+3469T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9871898 | |||||||
| chr2:9872094 | G | A | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.553+3665G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872094 | |||||||
| chr2:9872096 | C | T | 1 | a0005c0005t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.553+3667C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872096 | |||||||
| chr2:9872097 | G | A | 1 | a0002c0002t0001g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.553+3668G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872097 | |||||||
| chr2:9872199 | G | A | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.554-3666G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872199 | |||||||
| chr2:9872252 | G | A | 1 | a0005c0005t0001g0079 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.554-3613G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872252 | |||||||
| chr2:9872325 | T | TAA | 10 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(7): Show |
10 | HG01109.hp2 HG02258.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.554-3524_554-3523d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 9872325 | ||||||
| chr2:9872325 | TA | T | 129 | a0001c0001t0001g0261 a0002c0002t0001g0335 a0002c0002t0001g0336 others(126): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.554-3523delA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 9872325 | ||||||
| chr2:9872347 | C | G | 1 | a0001c0001t0002g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.554-3518C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872347 | |||||||
| chr2:9872860 | T | G | 84 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(81): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.554-3005T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872860 | |||||||
| chr2:9872941 | T | A | 335 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.554-2924T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872941 | |||||||
| chr2:9872979 | A | G | 8 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(5): Show |
8 | HG00099.hp1 HG01168.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.554-2886A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9872979 | |||||||
| chr2:9873070 | C | G | 6 | a0006c0006t0001g0014 a0006c0006t0001g0020 a0006c0006t0001g0021 others(3): Show |
6 | HG02257.hp1 HG02451.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.554-2795C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9873070 | |||||||
| chr2:9873269 | G | T | 1 | a0004c0003t0001g0274 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.554-2596G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9873269 | |||||||
| chr2:9873304 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.554-2561G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9873304 | |||||||
| chr2:9873551 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.554-2314G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9873551 | |||||||
| chr2:9873620 | A | AT | 7 | a0002c0002t0001g0133 a0002c0002t0001g0153 a0002c0002t0002g0134 others(4): Show |
7 | HG00735.hp2 HG01952.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.554-2225dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 9873620 | ||||||
| chr2:9873620 | AT | A | 119 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(116): Show |
128 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.554-2225delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 9873620 | ||||||
| chr2:9873620 | ATT | A | 11 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(8): Show |
11 | HG01070.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.554-2226_554-2225d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 9873620 | ||||||
| chr2:9873859 | G | A | 74 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(71): Show |
74 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.554-2006G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9873859 | |||||||
| chr2:9873914 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.554-1951G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9873914 | |||||||
| chr2:9874089 | C | A | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.554-1776C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9874089 | |||||||
| chr2:9874178 | T | C | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.554-1687T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9874178 | |||||||
| chr2:9874249 | A | G | 2 | a0005c0007t0001g0339 a0005c0007t0001g0340 |
2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.554-1616A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9874249 | |||||||
| chr2:9874278 | T | G | 77 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(74): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.554-1587T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9874278 | |||||||
| chr2:9874339 | T | C | 1 | a0014c0017t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.554-1526T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9874339 | |||||||
| chr2:9874499 | T | G | 40 | a0001c0001t0002g0041 a0005c0005t0001g0013 a0005c0005t0001g0070 others(37): Show |
40 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.554-1366T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9874499 | |||||||
| chr2:9875055 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.554-810A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875055 | |||||||
| chr2:9875066 | A | G | 2 | a0005c0007t0001g0339 a0005c0007t0001g0340 |
2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.554-799A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875066 | |||||||
| chr2:9875116 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.554-749T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875116 | |||||||
| chr2:9875139 | T | A | 74 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(71): Show |
74 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.554-726T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875139 | |||||||
| chr2:9875221 | C | T | 2 | a0003c0004t0001g0296 a0003c0004t0001g0297 |
2 | HG01346.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.554-644C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875221 | |||||||
| chr2:9875260 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.554-605G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875260 | |||||||
| chr2:9875285 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.554-580G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875285 | |||||||
| chr2:9875303 | A | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.554-562A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875303 | |||||||
| chr2:9875598 | C | T | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.554-267C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875598 | |||||||
| chr2:9875708 | G | A | 1 | a0003c0004t0001g0342 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.554-157G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875708 | |||||||
| chr2:9875738 | G | A | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.554-127G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875738 | |||||||
| chr2:9875750 | A | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.554-115A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 6/14 | chr2 | 9875750 | |||||||
| chr2:9876262 | T | G | 1 | a0006c0015t0001g0016 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.707+244T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876262 | |||||||
| chr2:9876469 | T | G | 1 | a0010c0014t0001g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.707+451T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876469 | |||||||
| chr2:9876480 | G | C | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.707+462G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876480 | |||||||
| chr2:9876498 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.707+480G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876498 | |||||||
| chr2:9876631 | T | C | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.707+613T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876631 | |||||||
| chr2:9876944 | G | A | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+926G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876944 | |||||||
| chr2:9876968 | A | G | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.707+950A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876968 | |||||||
| chr2:9876989 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.707+971A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9876989 | |||||||
| chr2:9877020 | A | G | 1 | a0004c0003t0001g0262 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.707+1002A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877020 | |||||||
| chr2:9877037 | G | A | 125 | a0001c0001t0001g0261 a0003c0004t0001g0010 a0003c0004t0001g0044 others(122): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.707+1019G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877037 | |||||||
| chr2:9877139 | G | T | 5 | a0005c0007t0001g0073 a0010c0014t0001g0072 a0010c0014t0001g0074 others(2): Show |
5 | HG00639.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.707+1121G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877139 | |||||||
| chr2:9877189 | C | G | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+1171C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877189 | |||||||
| chr2:9877303 | G | C | 74 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(71): Show |
74 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.707+1285G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877303 | |||||||
| chr2:9877382 | C | A | 1 | a0005c0005t0001g0082 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.707+1364C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877382 | |||||||
| chr2:9877437 | G | A | 1 | a0002c0002t0001g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.707+1419G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877437 | |||||||
| chr2:9877491 | A | G | 9 | a0003c0004t0001g0276 a0003c0004t0001g0318 a0003c0004t0001g0319 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.707+1473A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877491 | |||||||
| chr2:9877513 | T | C | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.707+1495T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877513 | |||||||
| chr2:9877714 | A | G | 1 | a0003c0004t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.707+1696A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877714 | |||||||
| chr2:9877747 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.707+1729C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877747 | |||||||
| chr2:9877796 | T | G | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.707+1778T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9877796 | |||||||
| chr2:9878033 | C | T | 1 | a0003c0004t0001g0295 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.707+2015C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9878033 | |||||||
| chr2:9878219 | C | CT | 71 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(68): Show |
71 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.707+2216dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9878219 | ||||||
| chr2:9878219 | CT | C | 57 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(54): Show |
58 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.707+2216delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9878219 | ||||||
| chr2:9878257 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.707+2239G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9878257 | |||||||
| chr2:9878323 | ACCTTGGC others(6): Show |
A | 2 | a0006c0006t0001g0015 a0006c0006t0001g0025 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.707+2317_707+2329d others(15): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9878323 | ||||||
| chr2:9878366 | T | G | 287 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(284): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.707+2348T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9878366 | |||||||
| chr2:9878551 | A | G | 1 | a0006c0006t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.707+2533A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9878551 | |||||||
| chr2:9878616 | A | G | 1 | a0002c0002t0001g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.707+2598A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9878616 | |||||||
| chr2:9878712 | C | T | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG02145.hp2 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.707+2694C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9878712 | |||||||
| chr2:9878861 | A | G | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+2843A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9878861 | |||||||
| chr2:9879032 | G | C | 2 | a0005c0007t0001g0339 a0005c0007t0001g0340 |
2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.707+3014G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879032 | |||||||
| chr2:9879147 | A | G | 66 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(63): Show |
66 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.707+3129A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879147 | |||||||
| chr2:9879403 | C | T | 126 | a0001c0001t0001g0261 a0003c0004t0001g0010 a0003c0004t0001g0044 others(123): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.708-3303C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879403 | |||||||
| chr2:9879571 | T | G | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-3135T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879571 | |||||||
| chr2:9879789 | A | G | 1 | a0005c0005t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.708-2917A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879789 | |||||||
| chr2:9879814 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.708-2892A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879814 | |||||||
| chr2:9879819 | A | G | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.708-2887A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879819 | |||||||
| chr2:9879847 | G | GT | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.708-2856dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9879847 | ||||||
| chr2:9879917 | C | T | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.708-2789C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879917 | |||||||
| chr2:9879961 | A | G | 7 | a0006c0006t0001g0014 a0006c0006t0001g0019 a0006c0006t0001g0020 others(4): Show |
7 | HG02257.hp1 HG02451.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.708-2745A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879961 | |||||||
| chr2:9879979 | T | C | 1 | a0003c0004t0001g0278 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.708-2727T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9879979 | |||||||
| chr2:9880007 | G | C | 3 | a0011c0010t0001g0352 a0011c0010t0001g0353 a0011c0010t0001g0354 |
3 | HG01109.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.708-2699G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880007 | |||||||
| chr2:9880039 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.708-2667G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880039 | |||||||
| chr2:9880353 | C | G | 1 | a0006c0006t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.708-2353C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880353 | |||||||
| chr2:9880426 | C | CT | 55 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(52): Show |
55 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.708-2255dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | C | CTT | 8 | a0002c0002t0001g0112 a0002c0002t0001g0152 a0002c0002t0002g0135 others(5): Show |
8 | HG01496.hp1 HG02056.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.708-2256_708-2255d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | C | CTTT | 6 | a0001c0001t0001g0179 a0001c0001t0002g0196 a0001c0001t0002g0206 others(3): Show |
6 | HG00733.hp2 HG02145.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-2257_708-2255d others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | C | CTTTT | 57 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0198 others(54): Show |
63 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.708-2258_708-2255d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | C | CTTTTT | 12 | a0001c0001t0001g0165 a0001c0001t0002g0003 a0001c0001t0002g0175 others(9): Show |
14 | HG00642.hp2 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.708-2259_708-2255d others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | CT | C | 14 | a0002c0002t0001g0063 a0003c0004t0001g0010 a0003c0004t0001g0282 others(11): Show |
15 | HG01167.hp1 HG01169.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.708-2255delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | CTTTTTTT others(4): Show |
C | 34 | a0005c0005t0001g0013 a0005c0005t0001g0070 a0005c0005t0001g0075 others(31): Show |
34 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.708-2265_708-2255d others(13): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | CTTTTTTT others(5): Show |
C | 5 | a0005c0005t0001g0105 a0005c0005t0001g0106 a0005c0005t0001g0107 others(2): Show |
5 | HG02027.hp2 NA18612.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.708-2266_708-2255d others(14): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880426 | CTTTTTTT others(6): Show |
C | 1 | a0003c0004t0001g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.708-2267_708-2255d others(15): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 9880426 | ||||||
| chr2:9880479 | G | A | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.708-2227G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880479 | |||||||
| chr2:9880530 | C | T | 74 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(71): Show |
74 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.708-2176C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880530 | |||||||
| chr2:9880548 | G | A | 1 | a0002c0002t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.708-2158G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880548 | |||||||
| chr2:9880595 | C | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0164 |
2 | NA19076.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.708-2111C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880595 | |||||||
| chr2:9880681 | G | T | 1 | a0002c0002t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.708-2025G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880681 | |||||||
| chr2:9880688 | G | A | 1 | a0002c0002t0001g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.708-2018G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880688 | |||||||
| chr2:9880818 | C | T | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-1888C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880818 | |||||||
| chr2:9880897 | C | A | 6 | a0003c0004t0001g0010 a0003c0004t0001g0279 a0003c0004t0001g0292 others(3): Show |
7 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.708-1809C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880897 | |||||||
| chr2:9880936 | G | A | 2 | a0004c0003t0001g0258 a0004c0003t0001g0264 |
2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.708-1770G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9880936 | |||||||
| chr2:9881330 | T | C | 82 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(79): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.708-1376T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9881330 | |||||||
| chr2:9881626 | A | G | 1 | a0004c0003t0001g0291 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.708-1080A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9881626 | |||||||
| chr2:9881798 | A | G | 2 | a0005c0005t0001g0084 a0005c0005t0001g0093 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.708-908A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9881798 | |||||||
| chr2:9881881 | A | G | 1 | a0003c0004t0001g0323 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.708-825A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9881881 | |||||||
| chr2:9881909 | A | T | 13 | a0003c0004t0001g0302 a0003c0004t0001g0306 a0003c0004t0001g0307 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.708-797A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9881909 | |||||||
| chr2:9882027 | C | A | 2 | a0006c0006t0001g0015 a0006c0006t0001g0025 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.708-679C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9882027 | |||||||
| chr2:9882029 | A | C | 1 | a0003c0016t0001g0259 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.708-677A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9882029 | |||||||
| chr2:9882196 | G | C | 1 | a0001c0001t0002g0345 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.708-510G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 7/14 | chr2 | 9882196 | |||||||
| chr2:9882887 | T | C | 50 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(47): Show |
50 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.807+82T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9882887 | |||||||
| chr2:9882976 | G | T | 50 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(47): Show |
50 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.807+171G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9882976 | |||||||
| chr2:9882985 | T | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0180 a0001c0001t0002g0196 others(2): Show |
6 | NA18974.hp1 NA18992.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+180T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9882985 | |||||||
| chr2:9883387 | C | T | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.807+582C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883387 | |||||||
| chr2:9883437 | T | C | 2 | a0005c0005t0001g0084 a0005c0005t0001g0093 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.807+632T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883437 | |||||||
| chr2:9883646 | G | A | 1 | a0002c0002t0001g0064 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.807+841G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883646 | |||||||
| chr2:9883729 | G | A | 1 | a0002c0002t0001g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807+924G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883729 | |||||||
| chr2:9883745 | C | T | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+940C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883745 | |||||||
| chr2:9883862 | C | T | 1 | a0006c0006t0001g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.807+1057C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883862 | |||||||
| chr2:9883878 | A | G | 73 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(70): Show |
73 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.807+1073A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883878 | |||||||
| chr2:9883924 | C | G | 12 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(9): Show |
12 | HG00323.hp1 HG01106.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.807+1119C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883924 | |||||||
| chr2:9883930 | G | T | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+1125G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883930 | |||||||
| chr2:9883982 | G | T | 128 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.807+1177G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9883982 | |||||||
| chr2:9884037 | G | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+1232G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884037 | |||||||
| chr2:9884182 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.807+1377C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884182 | |||||||
| chr2:9884214 | G | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+1409G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884214 | |||||||
| chr2:9884219 | C | T | 1 | a0004c0003t0001g0254 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.807+1414C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884219 | |||||||
| chr2:9884315 | A | G | 73 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(70): Show |
73 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.807+1510A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884315 | |||||||
| chr2:9884323 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+1518G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884323 | |||||||
| chr2:9884342 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.807+1537C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884342 | |||||||
| chr2:9884360 | G | A | 1 | a0004c0003t0001g0270 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.807+1555G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884360 | |||||||
| chr2:9884402 | T | C | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+1597T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884402 | |||||||
| chr2:9884508 | G | A | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+1703G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884508 | |||||||
| chr2:9884557 | G | C | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.807+1752G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884557 | |||||||
| chr2:9884560 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+1755A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884560 | |||||||
| chr2:9884701 | T | C | 1 | a0005c0005t0001g0343 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.807+1896T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884701 | |||||||
| chr2:9884720 | C | T | 125 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(122): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.807+1915C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884720 | |||||||
| chr2:9884729 | G | T | 3 | a0006c0006t0001g0026 a0006c0006t0001g0027 a0006c0006t0001g0028 |
3 | HG02615.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.807+1924G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884729 | |||||||
| chr2:9884751 | C | G | 1 | a0006c0006t0001g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.807+1946C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884751 | |||||||
| chr2:9884764 | C | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+1959C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884764 | |||||||
| chr2:9884900 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+2095G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9884900 | |||||||
| chr2:9885051 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.807+2246A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885051 | |||||||
| chr2:9885174 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.807+2369A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885174 | |||||||
| chr2:9885293 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+2488A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885293 | |||||||
| chr2:9885294 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.807+2489G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885294 | |||||||
| chr2:9885349 | A | G | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+2544A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885349 | |||||||
| chr2:9885434 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+2629G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885434 | |||||||
| chr2:9885531 | G | C | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+2726G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885531 | |||||||
| chr2:9885547 | A | G | 73 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(70): Show |
73 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.807+2742A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885547 | |||||||
| chr2:9885644 | G | T | 125 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(122): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.807+2839G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885644 | |||||||
| chr2:9885743 | G | GC | 20 | a0001c0001t0001g0163 a0002c0002t0001g0142 a0002c0002t0001g0151 others(17): Show |
20 | HG02056.hp2 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.807+2947dupC | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9885743 | ||||||
| chr2:9885745 | C | A | 1 | a0002c0002t0002g0135 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.807+2940C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885745 | |||||||
| chr2:9885753 | A | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+2948A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9885753 | |||||||
| chr2:9886097 | A | G | 222 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(219): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.807+3292A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886097 | |||||||
| chr2:9886119 | G | GC | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+3314_807+3315i others(3): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886119 | |||||||
| chr2:9886121 | C | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+3316C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886121 | |||||||
| chr2:9886125 | T | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+3320T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886125 | |||||||
| chr2:9886209 | C | CAA | 71 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(68): Show |
80 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.807+3414_807+3415d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9886209 | ||||||
| chr2:9886223 | C | G | 148 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(145): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.807+3418C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886223 | |||||||
| chr2:9886224 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+3419A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886224 | |||||||
| chr2:9886372 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.807+3567C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886372 | |||||||
| chr2:9886607 | A | T | 1 | a0002c0002t0001g0062 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.807+3802A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886607 | |||||||
| chr2:9886612 | C | A | 335 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.807+3807C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886612 | |||||||
| chr2:9886613 | T | C | 1 | a0001c0001t0002g0004 | 2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.807+3808T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886613 | |||||||
| chr2:9886673 | AAG | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+3880_807+3881d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9886673 | ||||||
| chr2:9886685 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.807+3880G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886685 | |||||||
| chr2:9886687 | T | G | 1 | a0003c0004t0001g0342 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.807+3882T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886687 | |||||||
| chr2:9886717 | A | G | 1 | a0002c0002t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.807+3912A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886717 | |||||||
| chr2:9886805 | G | A | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+4000G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886805 | |||||||
| chr2:9886842 | G | A | 41 | a0003c0016t0001g0207 a0003c0016t0001g0259 a0005c0005t0001g0013 others(38): Show |
41 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.807+4037G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886842 | |||||||
| chr2:9886846 | C | T | 1 | a0006c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.807+4041C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9886846 | |||||||
| chr2:9887063 | CA | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+4269delA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9887063 | ||||||
| chr2:9887184 | C | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+4379C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887184 | |||||||
| chr2:9887207 | GT | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+4405delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9887207 | ||||||
| chr2:9887294 | C | G | 1 | a0007c0008t0001g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.807+4489C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887294 | |||||||
| chr2:9887509 | G | A | 2 | a0005c0007t0001g0339 a0005c0007t0001g0340 |
2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.807+4704G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887509 | |||||||
| chr2:9887540 | G | A | 127 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.807+4735G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887540 | |||||||
| chr2:9887550 | G | GT | 333 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(330): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.807+4753dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9887550 | ||||||
| chr2:9887574 | G | A | 5 | a0005c0007t0001g0073 a0010c0014t0001g0072 a0010c0014t0001g0074 others(2): Show |
5 | HG00639.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+4769G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887574 | |||||||
| chr2:9887589 | A | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+4784A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887589 | |||||||
| chr2:9887716 | A | G | 5 | a0001c0001t0002g0041 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | NA18971.hp2 NA18975.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.807+4911A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887716 | |||||||
| chr2:9887949 | C | T | 1 | a0003c0004t0001g0328 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.807+5144C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9887949 | |||||||
| chr2:9888252 | C | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+5447C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888252 | |||||||
| chr2:9888254 | C | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.807+5449C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888254 | |||||||
| chr2:9888311 | A | ATT | 111 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(108): Show |
111 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.807+5515_807+5516d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888311 | ||||||
| chr2:9888482 | G | A | 1 | a0006c0006t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.807+5677G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888482 | |||||||
| chr2:9888568 | A | G | 148 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(145): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.807+5763A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888568 | |||||||
| chr2:9888594 | T | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.807+5789T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888594 | |||||||
| chr2:9888632 | T | C | 1 | a0003c0004t0004g0316 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.807+5827T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888632 | |||||||
| chr2:9888744 | A | C | 1 | a0002c0002t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.807+5939A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888744 | |||||||
| chr2:9888790 | G | GGTTTTT | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+5985_807+5986i others(8): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888790 | |||||||
| chr2:9888790 | G | GT | 23 | a0003c0004t0001g0260 a0003c0004t0001g0281 a0003c0004t0001g0288 others(20): Show |
23 | HG00741.hp2 HG01123.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.807+6015dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888790 | ||||||
| chr2:9888790 | G | GTT | 16 | a0003c0004t0001g0289 a0003c0004t0001g0313 a0003c0004t0001g0314 others(13): Show |
16 | HG00673.hp1 HG01106.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.807+6014_807+6015d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888790 | ||||||
| chr2:9888790 | G | T | 3 | a0004c0003t0001g0220 a0004c0003t0001g0221 a0006c0006t0001g0025 |
3 | HG03540.hp2 NA18965.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.807+5985G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888790 | |||||||
| chr2:9888790 | GT | G | 41 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(38): Show |
41 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.807+6015delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888790 | ||||||
| chr2:9888790 | GTTTT | G | 42 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(39): Show |
42 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.807+6012_807+6015d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888790 | ||||||
| chr2:9888790 | GTTTTTTT | G | 67 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(64): Show |
76 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.807+6009_807+6015d others(9): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888790 | ||||||
| chr2:9888790 | GTTTTTTT others(4): Show |
G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.807+6005_807+6015d others(13): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888790 | ||||||
| chr2:9888791 | T | G | 5 | a0002c0002t0001g0050 a0002c0002t0001g0063 a0005c0007t0001g0011 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.807+5986T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888791 | |||||||
| chr2:9888792 | T | G | 19 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(16): Show |
19 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.807+5987T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888792 | |||||||
| chr2:9888793 | T | G | 2 | a0002c0002t0001g0049 a0002c0002t0001g0111 |
2 | HG02040.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.807+5988T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888793 | |||||||
| chr2:9888794 | T | G | 5 | a0002c0002t0001g0115 a0002c0002t0001g0137 a0002c0002t0001g0150 others(2): Show |
5 | HG01106.hp2 HG01358.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+5989T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888794 | |||||||
| chr2:9888795 | T | G | 42 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(39): Show |
42 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.807+5990T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888795 | |||||||
| chr2:9888796 | T | G | 2 | a0002c0002t0001g0112 a0002c0002t0001g0114 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.807+5991T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888796 | |||||||
| chr2:9888797 | T | G | 6 | a0001c0001t0002g0211 a0002c0002t0001g0355 a0002c0002t0001g0356 others(3): Show |
6 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+5992T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888797 | |||||||
| chr2:9888798 | T | G | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.807+5993T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888798 | |||||||
| chr2:9888799 | T | G | 1 | a0009c0012t0001g0348 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.807+5994T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888799 | |||||||
| chr2:9888807 | T | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+6002T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888807 | |||||||
| chr2:9888808 | T | G | 1 | a0012c0013t0001g0051 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.807+6003T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888808 | |||||||
| chr2:9888809 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.807+6004T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888809 | |||||||
| chr2:9888810 | T | G | 67 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(64): Show |
76 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.807+6005T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888810 | |||||||
| chr2:9888907 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.807+6102G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888907 | |||||||
| chr2:9888934 | T | C | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.807+6129T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888934 | |||||||
| chr2:9888950 | T | C | 1 | a0006c0006t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.807+6145T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888950 | |||||||
| chr2:9888953 | G | A | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+6148G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9888953 | |||||||
| chr2:9888973 | T | TG | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+6169dupG | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9888973 | ||||||
| chr2:9889049 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.807+6244G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889049 | |||||||
| chr2:9889078 | G | A | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.807+6273G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889078 | |||||||
| chr2:9889311 | G | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+6506G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889311 | |||||||
| chr2:9889398 | T | G | 1 | a0005c0005t0001g0096 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.807+6593T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889398 | |||||||
| chr2:9889659 | G | A | 1 | a0003c0004t0001g0320 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.807+6854G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889659 | |||||||
| chr2:9889735 | T | C | 2 | a0004c0003t0001g0248 a0004c0003t0001g0317 |
2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.807+6930T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889735 | |||||||
| chr2:9889819 | A | G | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+7014A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889819 | |||||||
| chr2:9889824 | G | A | 337 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(334): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.807+7019G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889824 | |||||||
| chr2:9889895 | C | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+7090C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889895 | |||||||
| chr2:9889896 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.807+7091G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889896 | |||||||
| chr2:9889924 | G | T | 3 | a0005c0005t0001g0013 a0005c0005t0001g0084 a0005c0005t0001g0093 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.807+7119G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9889924 | |||||||
| chr2:9890018 | T | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+7213T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890018 | |||||||
| chr2:9890029 | CTCTG | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+7228_807+7231d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9890029 | ||||||
| chr2:9890370 | A | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.807+7565A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890370 | |||||||
| chr2:9890482 | T | C | 2 | a0002c0002t0001g0145 a0002c0002t0001g0150 |
2 | HG01106.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.807+7677T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890482 | |||||||
| chr2:9890487 | A | T | 267 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(264): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.807+7682A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890487 | |||||||
| chr2:9890488 | A | T | 1 | a0002c0002t0001g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.807+7683A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890488 | |||||||
| chr2:9890793 | G | A | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0022 |
3 | HG03139.hp2 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.807+7988G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890793 | |||||||
| chr2:9890835 | A | G | 78 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(75): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.807+8030A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890835 | |||||||
| chr2:9890839 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.807+8034A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890839 | |||||||
| chr2:9890918 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+8113G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890918 | |||||||
| chr2:9890927 | A | C | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.807+8122A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890927 | |||||||
| chr2:9890928 | T | G | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.807+8123T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890928 | |||||||
| chr2:9890960 | T | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+8155T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9890960 | |||||||
| chr2:9891000 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+8195G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891000 | |||||||
| chr2:9891032 | C | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+8227C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891032 | |||||||
| chr2:9891260 | T | G | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.807+8455T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891260 | |||||||
| chr2:9891275 | T | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+8470T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891275 | |||||||
| chr2:9891316 | G | A | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.807+8511G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891316 | |||||||
| chr2:9891457 | T | A | 3 | a0010c0014t0001g0072 a0010c0014t0001g0074 a0010c0014t0001g0337 |
3 | HG00639.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.807+8652T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891457 | |||||||
| chr2:9891614 | G | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+8809G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891614 | |||||||
| chr2:9891627 | C | T | 132 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(129): Show |
134 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.807+8822C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891627 | |||||||
| chr2:9891907 | A | G | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.807+9102A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891907 | |||||||
| chr2:9891912 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+9107G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9891912 | |||||||
| chr2:9892168 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+9363G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892168 | |||||||
| chr2:9892366 | C | T | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+9561C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892366 | |||||||
| chr2:9892410 | G | A | 4 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+9605G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892410 | |||||||
| chr2:9892472 | C | T | 3 | a0004c0003t0001g0247 a0004c0003t0001g0267 a0015c0019t0001g0237 |
3 | NA18941.hp2 NA18982.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.807+9667C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892472 | |||||||
| chr2:9892578 | T | C | 148 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(145): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.807+9773T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892578 | |||||||
| chr2:9892597 | G | A | 1 | a0003c0004t0001g0323 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.807+9792G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892597 | |||||||
| chr2:9892688 | A | C | 1 | a0005c0005t0001g0344 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.807+9883A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892688 | |||||||
| chr2:9892759 | AT | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+9962delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9892759 | ||||||
| chr2:9892879 | C | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+10074C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892879 | |||||||
| chr2:9892916 | C | T | 3 | a0010c0014t0001g0072 a0010c0014t0001g0074 a0010c0014t0001g0337 |
3 | HG00639.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.807+10111C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9892916 | |||||||
| chr2:9893142 | A | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+10337A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893142 | |||||||
| chr2:9893148 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+10343A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893148 | |||||||
| chr2:9893182 | G | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+10377G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893182 | |||||||
| chr2:9893301 | T | C | 1 | a0006c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.807+10496T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893301 | |||||||
| chr2:9893327 | G | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.807+10522G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893327 | |||||||
| chr2:9893413 | G | A | 3 | a0003c0004t0001g0306 a0003c0004t0001g0325 a0003c0004t0001g0326 |
3 | HG02257.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.807+10608G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893413 | |||||||
| chr2:9893420 | G | GA | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+10621dupA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9893420 | ||||||
| chr2:9893560 | G | A | 3 | a0002c0002t0001g0141 a0002c0002t0001g0146 a0002c0002t0001g0151 |
3 | HG01257.hp1 HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.807+10755G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893560 | |||||||
| chr2:9893621 | C | T | 152 | a0003c0004t0001g0010 a0003c0004t0001g0253 a0003c0004t0001g0260 others(149): Show |
154 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.807+10816C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893621 | |||||||
| chr2:9893641 | C | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.807+10836C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893641 | |||||||
| chr2:9893657 | C | T | 22 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(19): Show |
22 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.807+10852C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893657 | |||||||
| chr2:9893699 | C | T | 7 | a0005c0005t0001g0101 a0005c0005t0001g0104 a0005c0005t0001g0105 others(4): Show |
7 | HG00438.hp1 HG02027.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.807+10894C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893699 | |||||||
| chr2:9893734 | A | G | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG02145.hp2 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.807+10929A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893734 | |||||||
| chr2:9893753 | T | G | 2 | a0004c0003t0001g0248 a0004c0003t0001g0317 |
2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.807+10948T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893753 | |||||||
| chr2:9893797 | C | CTAGT | 168 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(165): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.807+10995_807+1099 others(8): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9893797 | ||||||
| chr2:9893839 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-11020G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9893839 | |||||||
| chr2:9894022 | G | A | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.808-10837G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9894022 | |||||||
| chr2:9894039 | A | T | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.808-10820A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9894039 | |||||||
| chr2:9894090 | A | AAATT | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-10768_808-1076 others(8): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9894090 | ||||||
| chr2:9894107 | CG | C | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-10751delG | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9894107 | |||||||
| chr2:9894110 | AT | A | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-10746delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9894110 | ||||||
| chr2:9894245 | C | CTT | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.808-10613_808-1061 others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9894245 | ||||||
| chr2:9894617 | T | C | 77 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(74): Show |
77 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.808-10242T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9894617 | |||||||
| chr2:9894747 | T | TGTTA | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-10111_808-1010 others(8): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9894747 | ||||||
| chr2:9894771 | G | A | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.808-10088G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9894771 | |||||||
| chr2:9894853 | A | G | 8 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(5): Show |
8 | HG01070.hp1 HG02258.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.808-10006A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9894853 | |||||||
| chr2:9895032 | A | G | 2 | a0003c0004t0001g0278 a0003c0004t0001g0298 |
2 | HG01175.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.808-9827A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9895032 | |||||||
| chr2:9895162 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-9697G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9895162 | |||||||
| chr2:9895238 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.808-9621G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9895238 | |||||||
| chr2:9895440 | G | A | 7 | a0005c0005t0001g0101 a0005c0005t0001g0104 a0005c0005t0001g0105 others(4): Show |
7 | HG00438.hp1 HG02027.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.808-9419G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9895440 | |||||||
| chr2:9895469 | A | G | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.808-9390A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9895469 | |||||||
| chr2:9895505 | GA | G | 210 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(207): Show |
212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.808-9343delA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9895505 | ||||||
| chr2:9895741 | T | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-9118T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9895741 | |||||||
| chr2:9895813 | C | CT | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(25): Show |
28 | HG01069.hp1 HG01071.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.808-9023dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9895813 | ||||||
| chr2:9895813 | C | CTT | 9 | a0001c0001t0001g0213 a0002c0002t0001g0060 a0002c0002t0001g0113 others(6): Show |
9 | HG00323.hp1 HG01070.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.808-9024_808-9023d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9895813 | ||||||
| chr2:9895813 | C | CTTT | 38 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(35): Show |
38 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.808-9025_808-9023d others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9895813 | ||||||
| chr2:9895813 | CT | C | 26 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(23): Show |
27 | HG00099.hp1 HG00323.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.808-9023delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9895813 | ||||||
| chr2:9895813 | CTT | C | 70 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(67): Show |
79 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.808-9024_808-9023d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9895813 | ||||||
| chr2:9895966 | T | C | 1 | a0003c0004t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.808-8893T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9895966 | |||||||
| chr2:9896130 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.808-8729G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896130 | |||||||
| chr2:9896137 | A | G | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.808-8722A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896137 | |||||||
| chr2:9896268 | T | G | 1 | a0003c0004t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.808-8591T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896268 | |||||||
| chr2:9896316 | A | T | 326 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(323): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.808-8543A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896316 | |||||||
| chr2:9896431 | C | T | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(65): Show |
77 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.808-8428C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896431 | |||||||
| chr2:9896620 | C | CA | 19 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0176 others(16): Show |
21 | HG01070.hp1 HG01109.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.808-8217dupA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9896620 | ||||||
| chr2:9896620 | CA | C | 175 | a0001c0001t0002g0004 a0001c0001t0002g0193 a0002c0002t0001g0146 others(172): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.808-8217delA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9896620 | ||||||
| chr2:9896642 | A | AAAT | 12 | a0001c0001t0001g0261 a0002c0002t0001g0064 a0002c0002t0001g0066 others(9): Show |
12 | HG02145.hp2 HG02559.hp1 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.808-8217_808-8216i others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896642 | |||||||
| chr2:9896642 | A | AAT | 54 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.808-8217_808-8216i others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896642 | |||||||
| chr2:9896642 | A | AT | 3 | a0002c0002t0001g0111 a0002c0002t0001g0140 a0012c0013t0001g0051 |
3 | HG02922.hp2 NA18948.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.808-8217_808-8216i others(3): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896642 | |||||||
| chr2:9896642 | A | T | 3 | a0002c0002t0001g0141 a0002c0002t0001g0146 a0002c0002t0001g0151 |
3 | HG01257.hp1 HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.808-8217A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896642 | |||||||
| chr2:9896681 | C | CTG | 148 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(145): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.808-8177_808-8176i others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9896681 | ||||||
| chr2:9896720 | C | T | 9 | a0003c0004t0001g0276 a0003c0004t0001g0318 a0003c0004t0001g0319 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.808-8139C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896720 | |||||||
| chr2:9896822 | A | G | 356 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(353): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.808-8037A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896822 | |||||||
| chr2:9896995 | G | A | 4 | a0004c0003t0001g0222 a0004c0003t0001g0223 a0004c0003t0001g0257 others(1): Show |
4 | NA18971.hp1 NA18972.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.808-7864G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9896995 | |||||||
| chr2:9897333 | A | C | 1 | a0005c0005t0001g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.808-7526A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897333 | |||||||
| chr2:9897366 | A | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-7493A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897366 | |||||||
| chr2:9897367 | C | T | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.808-7492C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897367 | |||||||
| chr2:9897417 | T | C | 6 | a0005c0005t0001g0104 a0005c0005t0001g0105 a0005c0005t0001g0106 others(3): Show |
6 | HG02027.hp2 NA18612.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-7442T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897417 | |||||||
| chr2:9897468 | G | T | 1 | a0005c0005t0001g0091 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.808-7391G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897468 | |||||||
| chr2:9897523 | T | A | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.808-7336T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897523 | |||||||
| chr2:9897710 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-7149G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897710 | |||||||
| chr2:9897872 | A | G | 329 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(326): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.808-6987A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897872 | |||||||
| chr2:9897895 | C | G | 2 | a0006c0006t0001g0024 a0013c0021t0001g0023 |
2 | HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.808-6964C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9897895 | |||||||
| chr2:9898097 | G | A | 148 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(145): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.808-6762G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898097 | |||||||
| chr2:9898132 | C | T | 7 | a0005c0007t0001g0052 a0005c0007t0001g0056 a0005c0007t0001g0057 others(4): Show |
7 | HG01496.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.808-6727C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898132 | |||||||
| chr2:9898170 | T | C | 22 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(19): Show |
22 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.808-6689T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898170 | |||||||
| chr2:9898562 | T | G | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.808-6297T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898562 | |||||||
| chr2:9898572 | G | C | 165 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(162): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.808-6287G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898572 | |||||||
| chr2:9898607 | C | A | 335 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.808-6252C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898607 | |||||||
| chr2:9898736 | G | A | 7 | a0001c0001t0002g0191 a0005c0011t0001g0349 a0005c0011t0001g0350 others(4): Show |
7 | HG00741.hp1 HG01070.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.808-6123G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898736 | |||||||
| chr2:9898747 | A | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-6112A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898747 | |||||||
| chr2:9898761 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-6098A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898761 | |||||||
| chr2:9898769 | T | C | 4 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-6090T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898769 | |||||||
| chr2:9898796 | A | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.808-6063A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898796 | |||||||
| chr2:9898925 | AC | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-5933delC | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9898925 | |||||||
| chr2:9898938 | CT | C | 75 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(72): Show |
75 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.808-5910delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9898938 | ||||||
| chr2:9899012 | C | T | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.808-5847C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899012 | |||||||
| chr2:9899038 | G | GT | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-5820dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9899038 | ||||||
| chr2:9899076 | T | G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.808-5783T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899076 | |||||||
| chr2:9899123 | C | T | 22 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(19): Show |
22 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.808-5736C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899123 | |||||||
| chr2:9899321 | C | T | 2 | a0004c0003t0001g0258 a0004c0003t0001g0264 |
2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.808-5538C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899321 | |||||||
| chr2:9899322 | C | T | 2 | a0004c0003t0001g0043 a0004c0003t0001g0268 |
2 | HG02056.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.808-5537C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899322 | |||||||
| chr2:9899460 | A | G | 340 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(337): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.808-5399A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899460 | |||||||
| chr2:9899493 | T | A | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-5366T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899493 | |||||||
| chr2:9899525 | G | A | 50 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(47): Show |
50 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.808-5334G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899525 | |||||||
| chr2:9899665 | TG | T | 135 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.808-5193delG | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899665 | |||||||
| chr2:9899667 | T | A | 5 | a0005c0007t0001g0052 a0005c0007t0001g0056 a0005c0007t0001g0057 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.808-5192T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899667 | |||||||
| chr2:9899685 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-5174A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899685 | |||||||
| chr2:9899689 | ATGTAT | A | 76 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(73): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.808-5168_808-5164d others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9899689 | ||||||
| chr2:9899729 | G | A | 2 | a0005c0007t0001g0339 a0005c0007t0001g0340 |
2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.808-5130G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899729 | |||||||
| chr2:9899892 | TATGA | T | 3 | a0004c0003t0001g0216 a0004c0003t0001g0217 a0004c0003t0001g0218 |
3 | NA18970.hp2 NA19011.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.808-4964_808-4961d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9899892 | ||||||
| chr2:9899899 | A | T | 3 | a0004c0003t0001g0216 a0004c0003t0001g0217 a0004c0003t0001g0218 |
3 | NA18970.hp2 NA19011.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.808-4960A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899899 | |||||||
| chr2:9899953 | A | T | 1 | a0004c0003t0001g0262 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.808-4906A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899953 | |||||||
| chr2:9899954 | T | A | 1 | a0004c0003t0001g0262 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.808-4905T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899954 | |||||||
| chr2:9899969 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-4890G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9899969 | |||||||
| chr2:9900145 | A | G | 1 | a0006c0006t0001g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.808-4714A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900145 | |||||||
| chr2:9900222 | A | G | 136 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(133): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.808-4637A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900222 | |||||||
| chr2:9900312 | T | C | 1 | a0002c0002t0001g0336 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.808-4547T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900312 | |||||||
| chr2:9900362 | C | T | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.808-4497C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900362 | |||||||
| chr2:9900389 | G | A | 1 | a0003c0004t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.808-4470G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900389 | |||||||
| chr2:9900418 | T | C | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.808-4441T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900418 | |||||||
| chr2:9900543 | A | T | 133 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(130): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.808-4316A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900543 | |||||||
| chr2:9900547 | T | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.808-4312T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900547 | |||||||
| chr2:9900709 | T | C | 1 | a0002c0002t0002g0130 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.808-4150T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9900709 | |||||||
| chr2:9901117 | G | A | 2 | a0004c0003t0001g0248 a0004c0003t0001g0317 |
2 | NA18984.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.808-3742G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901117 | |||||||
| chr2:9901155 | A | C | 223 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(220): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.808-3704A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901155 | |||||||
| chr2:9901186 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.808-3673G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901186 | |||||||
| chr2:9901199 | T | C | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.808-3660T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901199 | |||||||
| chr2:9901325 | T | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-3534T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901325 | |||||||
| chr2:9901332 | T | C | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.808-3527T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901332 | |||||||
| chr2:9901358 | TTAA | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-3496_808-3494d others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9901358 | ||||||
| chr2:9901420 | T | G | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.808-3439T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901420 | |||||||
| chr2:9901524 | T | C | 4 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-3335T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901524 | |||||||
| chr2:9901557 | G | T | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.808-3302G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901557 | |||||||
| chr2:9901894 | A | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-2965A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9901894 | |||||||
| chr2:9902019 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-2840G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902019 | |||||||
| chr2:9902150 | A | G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.808-2709A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902150 | |||||||
| chr2:9902157 | C | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-2702C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902157 | |||||||
| chr2:9902227 | CT | C | 201 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(198): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.808-2616delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 9902227 | ||||||
| chr2:9902228 | T | A | 2 | a0002c0002t0001g0115 a0002c0002t0001g0122 |
2 | HG03098.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.808-2631T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902228 | |||||||
| chr2:9902229 | T | A | 69 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(66): Show |
69 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.808-2630T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902229 | |||||||
| chr2:9902230 | T | A | 1 | a0002c0002t0002g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.808-2629T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902230 | |||||||
| chr2:9902270 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-2589G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902270 | |||||||
| chr2:9902300 | G | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-2559G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902300 | |||||||
| chr2:9902320 | T | C | 335 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(332): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.808-2539T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902320 | |||||||
| chr2:9902356 | G | A | 1 | a0002c0002t0002g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.808-2503G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902356 | |||||||
| chr2:9902358 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-2501A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902358 | |||||||
| chr2:9902373 | C | G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.808-2486C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902373 | |||||||
| chr2:9902564 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-2295A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902564 | |||||||
| chr2:9902660 | T | C | 128 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.808-2199T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902660 | |||||||
| chr2:9902765 | G | A | 41 | a0003c0016t0001g0207 a0003c0016t0001g0259 a0005c0005t0001g0013 others(38): Show |
41 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.808-2094G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902765 | |||||||
| chr2:9902885 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-1974G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902885 | |||||||
| chr2:9902901 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.808-1958A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902901 | |||||||
| chr2:9902936 | C | G | 1 | a0003c0004t0001g0295 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.808-1923C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902936 | |||||||
| chr2:9902946 | A | G | 11 | a0004c0003t0001g0034 a0004c0003t0001g0231 a0004c0003t0001g0246 others(8): Show |
11 | HG00438.hp2 HG01106.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.808-1913A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9902946 | |||||||
| chr2:9903019 | C | T | 1 | a0005c0005t0001g0104 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.808-1840C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903019 | |||||||
| chr2:9903121 | T | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-1738T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903121 | |||||||
| chr2:9903178 | T | C | 1 | a0003c0004t0001g0283 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.808-1681T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903178 | |||||||
| chr2:9903275 | G | T | 149 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(146): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.808-1584G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903275 | |||||||
| chr2:9903375 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-1484G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903375 | |||||||
| chr2:9903376 | T | C | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.808-1483T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903376 | |||||||
| chr2:9903381 | T | C | 149 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(146): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.808-1478T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903381 | |||||||
| chr2:9903452 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-1407G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903452 | |||||||
| chr2:9903578 | T | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-1281T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903578 | |||||||
| chr2:9903645 | C | T | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.808-1214C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9903645 | |||||||
| chr2:9904027 | A | C | 2 | a0005c0007t0001g0339 a0005c0007t0001g0340 |
2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.808-832A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904027 | |||||||
| chr2:9904072 | T | C | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.808-787T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904072 | |||||||
| chr2:9904076 | T | C | 146 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(143): Show |
155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.808-783T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904076 | |||||||
| chr2:9904091 | T | C | 3 | a0002c0002t0001g0124 a0002c0002t0001g0127 a0002c0002t0001g0128 |
3 | HG00280.hp1 HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.808-768T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904091 | |||||||
| chr2:9904283 | T | C | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.808-576T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904283 | |||||||
| chr2:9904286 | G | A | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.808-573G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904286 | |||||||
| chr2:9904311 | C | A | 143 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(140): Show |
152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.808-548C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904311 | |||||||
| chr2:9904414 | C | A | 75 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.808-445C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904414 | |||||||
| chr2:9904414 | C | G | 1 | a0003c0004t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.808-445C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904414 | |||||||
| chr2:9904698 | G | A | 149 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(146): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.808-161G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904698 | |||||||
| chr2:9904746 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.808-113A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904746 | |||||||
| chr2:9904781 | A | T | 3 | a0010c0014t0001g0072 a0010c0014t0001g0074 a0010c0014t0001g0337 |
3 | HG00639.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.808-78A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904781 | |||||||
| chr2:9904812 | G | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.808-47G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904812 | |||||||
| chr2:9904817 | G | T | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-42G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904817 | |||||||
| chr2:9904822 | A | G | 128 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.808-37A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 8/14 | chr2 | 9904822 | |||||||
| chr2:9905018 | A | G | 340 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(337): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.955+12A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905018 | |||||||
| chr2:9905272 | G | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+266G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905272 | |||||||
| chr2:9905345 | A | G | 16 | a0003c0004t0001g0253 a0003c0004t0001g0280 a0003c0004t0001g0281 others(13): Show |
16 | HG01123.hp1 HG01516.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.955+339A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905345 | |||||||
| chr2:9905416 | A | G | 3 | a0002c0002t0001g0141 a0002c0002t0001g0146 a0002c0002t0001g0151 |
3 | HG01257.hp1 HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.955+410A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905416 | |||||||
| chr2:9905435 | T | C | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.955+429T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905435 | |||||||
| chr2:9905512 | A | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+506A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905512 | |||||||
| chr2:9905526 | T | C | 9 | a0003c0004t0001g0276 a0003c0004t0001g0318 a0003c0004t0001g0319 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+520T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905526 | |||||||
| chr2:9905553 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.955+547C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905553 | |||||||
| chr2:9905588 | G | A | 139 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(136): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.955+582G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905588 | |||||||
| chr2:9905624 | T | C | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+618T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905624 | |||||||
| chr2:9905707 | C | CA | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+702dupA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9905707 | ||||||
| chr2:9905738 | A | G | 1 | a0002c0002t0001g0113 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955+732A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905738 | |||||||
| chr2:9905795 | T | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+789T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905795 | |||||||
| chr2:9905815 | A | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0209 a0001c0001t0002g0210 |
5 | NA18945.hp2 NA18954.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.955+809A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905815 | |||||||
| chr2:9905830 | CAT | C | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.955+830_955+831del others(2): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9905830 | ||||||
| chr2:9905867 | T | C | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.955+861T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905867 | |||||||
| chr2:9905872 | T | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+866T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905872 | |||||||
| chr2:9905938 | C | G | 1 | a0002c0002t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.955+932C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9905938 | |||||||
| chr2:9906041 | AT | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+1045delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9906041 | ||||||
| chr2:9906045 | T | A | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+1039T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906045 | |||||||
| chr2:9906094 | T | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.955+1088T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906094 | |||||||
| chr2:9906154 | A | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+1148A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906154 | |||||||
| chr2:9906333 | C | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+1327C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906333 | |||||||
| chr2:9906444 | G | T | 1 | a0004c0003t0001g0032 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.955+1438G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906444 | |||||||
| chr2:9906568 | C | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+1562C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906568 | |||||||
| chr2:9906668 | C | G | 2 | a0005c0005t0001g0096 a0005c0005t0001g0100 |
2 | HG02080.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.955+1662C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906668 | |||||||
| chr2:9906691 | C | T | 1 | a0005c0005t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.955+1685C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906691 | |||||||
| chr2:9906692 | G | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+1686G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906692 | |||||||
| chr2:9906730 | T | G | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.955+1724T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906730 | |||||||
| chr2:9906766 | A | G | 2 | a0002c0002t0001g0145 a0002c0002t0001g0150 |
2 | HG01106.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.955+1760A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906766 | |||||||
| chr2:9906887 | G | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+1881G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9906887 | |||||||
| chr2:9907071 | A | AAG | 5 | a0005c0007t0001g0052 a0005c0007t0001g0056 a0005c0007t0001g0057 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.955+2065_955+2066i others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907071 | |||||||
| chr2:9907072 | G | A | 5 | a0005c0007t0001g0052 a0005c0007t0001g0056 a0005c0007t0001g0057 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.955+2066G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907072 | |||||||
| chr2:9907074 | G | C | 5 | a0005c0007t0001g0052 a0005c0007t0001g0056 a0005c0007t0001g0057 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.955+2068G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907074 | |||||||
| chr2:9907189 | G | GT | 47 | a0003c0016t0001g0207 a0003c0016t0001g0259 a0004c0003t0001g0221 others(44): Show |
47 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.955+2198dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9907189 | ||||||
| chr2:9907189 | GT | G | 74 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(71): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.955+2198delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9907189 | ||||||
| chr2:9907189 | GTT | G | 73 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(70): Show |
73 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.955+2197_955+2198d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9907189 | ||||||
| chr2:9907194 | T | G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955+2188T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907194 | |||||||
| chr2:9907278 | G | A | 3 | a0003c0004t0001g0044 a0003c0004t0001g0299 a0003c0004t0001g0300 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.955+2272G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907278 | |||||||
| chr2:9907367 | G | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.955+2361G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907367 | |||||||
| chr2:9907378 | A | G | 338 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(335): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.955+2372A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907378 | |||||||
| chr2:9907543 | C | G | 129 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(126): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.955+2537C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907543 | |||||||
| chr2:9907620 | C | T | 1 | a0004c0003t0001g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.955+2614C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907620 | |||||||
| chr2:9907699 | T | C | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.955+2693T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907699 | |||||||
| chr2:9907771 | G | T | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.955+2765G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907771 | |||||||
| chr2:9907973 | C | T | 166 | a0003c0004t0001g0044 a0003c0004t0001g0253 a0003c0004t0001g0260 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.956-2763C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9907973 | |||||||
| chr2:9908027 | T | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.956-2709T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908027 | |||||||
| chr2:9908028 | C | CT | 17 | a0003c0004t0001g0287 a0003c0004t0001g0295 a0003c0004t0001g0301 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.956-2673dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | C | CTT | 23 | a0003c0004t0001g0286 a0003c0004t0001g0294 a0003c0004t0001g0321 others(20): Show |
24 | HG01192.hp2 HG01517.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.956-2674_956-2673d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | C | CTTT | 10 | a0003c0004t0001g0276 a0003c0004t0001g0322 a0003c0004t0001g0324 others(7): Show |
10 | HG00438.hp1 HG01257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-2675_956-2673d others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | C | CTTTT | 6 | a0003c0004t0001g0320 a0005c0005t0001g0095 a0005c0005t0001g0344 others(3): Show |
6 | HG02965.hp1 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.956-2676_956-2673d others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CT | C | 50 | a0003c0004t0001g0253 a0003c0004t0001g0260 a0003c0004t0001g0281 others(47): Show |
50 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.956-2673delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTT | C | 47 | a0003c0004t0001g0282 a0003c0004t0001g0283 a0003c0004t0001g0284 others(44): Show |
50 | HG01109.hp1 HG01256.hp1 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.956-2674_956-2673d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTTTTTTT | C | 8 | a0001c0001t0001g0213 a0002c0002t0001g0115 a0002c0002t0001g0143 others(5): Show |
8 | HG01070.hp2 HG02148.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.956-2679_956-2673d others(9): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTTTTTTT others(1): Show |
C | 54 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0261 others(51): Show |
54 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.956-2680_956-2673d others(10): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTTTTTTT others(2): Show |
C | 84 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(81): Show |
93 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.956-2681_956-2673d others(11): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTTTTTTT others(3): Show |
C | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.956-2682_956-2673d others(12): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTTTTTTT others(6): Show |
C | 2 | a0005c0005t0001g0103 a0007c0008t0001g0229 |
2 | HG06807.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.956-2685_956-2673d others(15): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTTTTTTT others(7): Show |
C | 1 | a0003c0004t0001g0293 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.956-2686_956-2673d others(16): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908028 | CTTTTTTT others(8): Show |
C | 2 | a0003c0004t0001g0292 a0004c0003t0001g0265 |
2 | HG03579.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.956-2687_956-2673d others(17): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908028 | ||||||
| chr2:9908072 | G | A | 1 | a0004c0003t0001g0332 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.956-2664G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908072 | |||||||
| chr2:9908104 | GGC | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-2630_956-2629d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908104 | ||||||
| chr2:9908106 | CGT | C | 146 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(143): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.956-2628_956-2627d others(4): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9908106 | ||||||
| chr2:9908267 | G | C | 1 | a0002c0002t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.956-2469G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908267 | |||||||
| chr2:9908327 | G | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.956-2409G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908327 | |||||||
| chr2:9908362 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.956-2374A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908362 | |||||||
| chr2:9908462 | A | G | 1 | a0005c0007t0001g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.956-2274A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908462 | |||||||
| chr2:9908650 | C | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.956-2086C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908650 | |||||||
| chr2:9908654 | A | G | 168 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(165): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.956-2082A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908654 | |||||||
| chr2:9908686 | C | T | 22 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(19): Show |
22 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.956-2050C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908686 | |||||||
| chr2:9908692 | T | A | 2 | a0001c0001t0002g0157 a0001c0001t0002g0164 |
2 | NA19076.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.956-2044T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908692 | |||||||
| chr2:9908811 | C | G | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-1925C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908811 | |||||||
| chr2:9908834 | C | T | 1 | a0003c0004t0001g0283 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.956-1902C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9908834 | |||||||
| chr2:9909029 | C | T | 1 | a0005c0005t0001g0098 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.956-1707C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909029 | |||||||
| chr2:9909104 | A | G | 3 | a0010c0014t0001g0072 a0010c0014t0001g0074 a0010c0014t0001g0337 |
3 | HG00639.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.956-1632A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909104 | |||||||
| chr2:9909108 | C | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.956-1628C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909108 | |||||||
| chr2:9909236 | C | A | 3 | a0004c0003t0001g0032 a0004c0003t0001g0042 a0004c0003t0001g0227 |
3 | HG01256.hp1 HG01496.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.956-1500C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909236 | |||||||
| chr2:9909253 | G | A | 3 | a0002c0002t0001g0119 a0002c0002t0001g0121 a0002c0002t0001g0122 |
3 | HG00642.hp1 HG01167.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.956-1483G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909253 | |||||||
| chr2:9909269 | C | T | 3 | a0003c0016t0001g0207 a0005c0005t0001g0097 a0005c0005t0001g0099 |
3 | NA18974.hp2 NA18998.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.956-1467C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909269 | |||||||
| chr2:9909311 | T | G | 1 | a0002c0002t0001g0046 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.956-1425T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909311 | |||||||
| chr2:9909372 | G | A | 189 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.956-1364G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909372 | |||||||
| chr2:9909449 | A | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0194 |
2 | HG01175.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.956-1287A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909449 | |||||||
| chr2:9909521 | T | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.956-1215T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909521 | |||||||
| chr2:9909569 | C | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.956-1167C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909569 | |||||||
| chr2:9909569 | C | T | 148 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(145): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.956-1167C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909569 | |||||||
| chr2:9909587 | C | T | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-1149C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909587 | |||||||
| chr2:9909663 | C | T | 1 | a0014c0017t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.956-1073C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909663 | |||||||
| chr2:9909744 | C | T | 143 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.956-992C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909744 | |||||||
| chr2:9909897 | C | G | 1 | a0005c0005t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.956-839C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9909897 | |||||||
| chr2:9910015 | G | C | 1 | a0002c0002t0001g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.956-721G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910015 | |||||||
| chr2:9910032 | T | TGATTAGA others(5): Show |
151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.956-703_956-702ins others(12): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 9910032 | ||||||
| chr2:9910134 | T | C | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-602T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910134 | |||||||
| chr2:9910145 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.956-591A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910145 | |||||||
| chr2:9910196 | A | G | 41 | a0003c0016t0001g0207 a0003c0016t0001g0259 a0005c0005t0001g0013 others(38): Show |
41 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.956-540A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910196 | |||||||
| chr2:9910209 | C | G | 1 | a0003c0004t0001g0305 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.956-527C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910209 | |||||||
| chr2:9910426 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.956-310G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910426 | |||||||
| chr2:9910549 | C | T | 1 | a0003c0004t0001g0010 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-187C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910549 | |||||||
| chr2:9910582 | T | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-154T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 9/14 | chr2 | 9910582 | |||||||
| chr2:9910924 | G | A | 1 | a0005c0007t0001g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1133+11G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/14 | chr2 | 9910924 | |||||||
| chr2:9910924 | G | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1133+11G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/14 | chr2 | 9910924 | |||||||
| chr2:9911032 | T | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1133+119T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/14 | chr2 | 9911032 | |||||||
| chr2:9911087 | A | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0208 a0001c0001t0002g0209 others(2): Show |
7 | NA18945.hp2 NA18954.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1133+174A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/14 | chr2 | 9911087 | |||||||
| chr2:9911284 | G | A | 1 | a0005c0005t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1134-227G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 10/14 | chr2 | 9911284 | |||||||
| chr2:9911663 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1180+106A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9911663 | |||||||
| chr2:9911863 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1180+306T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9911863 | |||||||
| chr2:9912003 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1180+446A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912003 | |||||||
| chr2:9912082 | T | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1180+525T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912082 | |||||||
| chr2:9912128 | G | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1180+571G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912128 | |||||||
| chr2:9912199 | T | C | 1 | a0003c0016t0001g0259 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1180+642T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912199 | |||||||
| chr2:9912255 | CT | C | 11 | a0001c0001t0002g0166 a0002c0002t0001g0355 a0002c0002t0001g0356 others(8): Show |
11 | HG00099.hp1 HG01168.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1180+711delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 9912255 | ||||||
| chr2:9912263 | T | C | 4 | a0005c0007t0001g0073 a0010c0014t0001g0072 a0010c0014t0001g0074 others(1): Show |
4 | HG00639.hp2 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+706T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912263 | |||||||
| chr2:9912370 | ATGTTC | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1181-782_1181-778d others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 9912370 | ||||||
| chr2:9912416 | G | T | 1 | a0001c0001t0002g0173 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1181-743G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912416 | |||||||
| chr2:9912751 | A | G | 40 | a0003c0016t0001g0207 a0003c0016t0001g0259 a0005c0005t0001g0013 others(37): Show |
40 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1181-408A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912751 | |||||||
| chr2:9912814 | G | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1181-345G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 11/14 | chr2 | 9912814 | |||||||
| chr2:9913283 | C | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1271+34C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9913283 | |||||||
| chr2:9913451 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1271+202G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9913451 | |||||||
| chr2:9913481 | A | G | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1271+232A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9913481 | |||||||
| chr2:9913769 | T | A | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1271+520T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9913769 | |||||||
| chr2:9913878 | T | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1271+629T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9913878 | |||||||
| chr2:9914004 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1271+755A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914004 | |||||||
| chr2:9914180 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1271+931A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914180 | |||||||
| chr2:9914273 | G | A | 14 | a0005c0005t0001g0075 a0005c0005t0001g0076 a0005c0005t0001g0077 others(11): Show |
14 | HG00597.hp1 HG02015.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1271+1024G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914273 | |||||||
| chr2:9914295 | C | A | 1 | a0003c0004t0001g0289 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1271+1046C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914295 | |||||||
| chr2:9914327 | T | C | 356 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(353): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1271+1078T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914327 | |||||||
| chr2:9914834 | C | T | 1 | a0005c0011t0001g0349 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1271+1585C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914834 | |||||||
| chr2:9914838 | G | A | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1271+1589G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914838 | |||||||
| chr2:9914870 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1271+1621A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914870 | |||||||
| chr2:9914945 | T | A | 1 | a0005c0005t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1271+1696T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9914945 | |||||||
| chr2:9915073 | C | T | 2 | a0003c0004t0001g0325 a0003c0004t0001g0326 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1271+1824C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915073 | |||||||
| chr2:9915084 | A | G | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1271+1835A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915084 | |||||||
| chr2:9915402 | G | A | 1 | a0006c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1271+2153G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915402 | |||||||
| chr2:9915426 | T | C | 168 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(165): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1271+2177T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915426 | |||||||
| chr2:9915493 | C | T | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271+2244C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915493 | |||||||
| chr2:9915494 | G | A | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1271+2245G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915494 | |||||||
| chr2:9915640 | C | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1271+2391C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915640 | |||||||
| chr2:9915664 | C | T | 153 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(150): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1271+2415C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915664 | |||||||
| chr2:9915782 | T | G | 1 | a0001c0001t0002g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1271+2533T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915782 | |||||||
| chr2:9915908 | A | ACTT | 187 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(184): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1271+2663_1271+266 others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9915908 | ||||||
| chr2:9915987 | T | A | 4 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1271+2738T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9915987 | |||||||
| chr2:9916268 | T | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-2773T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916268 | |||||||
| chr2:9916269 | A | G | 1 | a0002c0002t0001g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1272-2772A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916269 | |||||||
| chr2:9916283 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-2758A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916283 | |||||||
| chr2:9916311 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1272-2730C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916311 | |||||||
| chr2:9916330 | A | T | 1 | a0007c0008t0001g0244 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1272-2711A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916330 | |||||||
| chr2:9916389 | G | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-2652G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916389 | |||||||
| chr2:9916446 | C | T | 1 | a0014c0017t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1272-2595C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916446 | |||||||
| chr2:9916729 | A | G | 140 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(137): Show |
143 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1272-2312A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916729 | |||||||
| chr2:9916750 | T | C | 2 | a0006c0006t0001g0015 a0006c0006t0001g0025 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1272-2291T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916750 | |||||||
| chr2:9916834 | G | GTTGTTTT others(21): Show |
1 | a0002c0002t0001g0359 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1272-2205_1272-220 others(32): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916834 | ||||||
| chr2:9916834 | G | GTTGTTTT others(22): Show |
2 | a0002c0002t0001g0355 a0002c0002t0001g0358 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1272-2205_1272-220 others(33): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916834 | ||||||
| chr2:9916834 | G | GTTGTTTT others(24): Show |
1 | a0002c0002t0001g0356 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1272-2205_1272-220 others(35): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916834 | ||||||
| chr2:9916834 | G | GTTGTTTT others(29): Show |
1 | a0002c0002t0001g0357 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1272-2205_1272-220 others(40): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916834 | ||||||
| chr2:9916837 | C | CTTTTTT | 65 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(62): Show |
74 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1272-2191_1272-218 others(10): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | C | CTTTTTTT others(3): Show |
29 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0261 others(26): Show |
29 | HG00280.hp1 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1272-2195_1272-218 others(14): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | C | CTTTTTTT others(4): Show |
29 | a0001c0001t0001g0212 a0002c0002t0001g0046 a0002c0002t0001g0047 others(26): Show |
29 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1272-2196_1272-218 others(15): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | C | CTTTTTTT others(5): Show |
10 | a0002c0002t0001g0048 a0002c0002t0001g0063 a0002c0002t0001g0066 others(7): Show |
10 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272-2197_1272-218 others(16): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | C | CTTTTTTT others(6): Show |
3 | a0002c0002t0001g0064 a0002c0002t0001g0065 a0002c0002t0001g0069 |
3 | HG00609.hp1 NA18943.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1272-2198_1272-218 others(17): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | C | CTTTTTTT others(7): Show |
1 | a0002c0002t0001g0068 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1272-2199_1272-218 others(18): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | C | CTTTTTTT others(8): Show |
1 | a0002c0002t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1272-2200_1272-218 others(19): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | C | T | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1272-2204C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916837 | |||||||
| chr2:9916837 | CT | C | 45 | a0003c0004t0001g0277 a0003c0016t0001g0207 a0003c0016t0001g0259 others(42): Show |
45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1272-2186delT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916837 | CTT | C | 137 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1272-2187_1272-218 others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9916837 | ||||||
| chr2:9916911 | A | T | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1272-2130A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916911 | |||||||
| chr2:9916913 | C | T | 1 | a0005c0007t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1272-2128C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916913 | |||||||
| chr2:9916923 | C | T | 8 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(5): Show |
8 | HG01109.hp2 HG02258.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-2118C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916923 | |||||||
| chr2:9916933 | G | A | 22 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(19): Show |
22 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1272-2108G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9916933 | |||||||
| chr2:9917046 | A | G | 69 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(66): Show |
78 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1272-1995A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917046 | |||||||
| chr2:9917075 | A | G | 19 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(16): Show |
22 | HG00280.hp2 HG02040.hp1 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1272-1966A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917075 | |||||||
| chr2:9917307 | T | G | 72 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(69): Show |
81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1272-1734T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917307 | |||||||
| chr2:9917423 | C | T | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1272-1618C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917423 | |||||||
| chr2:9917440 | A | C | 1 | a0001c0001t0002g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1272-1601A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917440 | |||||||
| chr2:9917476 | GTATC | G | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1272-1562_1272-155 others(8): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9917476 | ||||||
| chr2:9917489 | A | C | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG02145.hp2 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1272-1552A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917489 | |||||||
| chr2:9917541 | G | A | 1 | a0002c0002t0001g0063 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1272-1500G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917541 | |||||||
| chr2:9917546 | A | G | 152 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(149): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1272-1495A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917546 | |||||||
| chr2:9917598 | G | A | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1272-1443G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917598 | |||||||
| chr2:9917638 | C | G | 1 | a0003c0004t0004g0245 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1272-1403C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917638 | |||||||
| chr2:9917843 | C | A | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1272-1198C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917843 | |||||||
| chr2:9917848 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1272-1193G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917848 | |||||||
| chr2:9917868 | T | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-1173T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917868 | |||||||
| chr2:9917900 | G | C | 3 | a0010c0014t0001g0072 a0010c0014t0001g0074 a0010c0014t0001g0337 |
3 | HG00639.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1272-1141G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917900 | |||||||
| chr2:9917912 | A | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1272-1129A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917912 | |||||||
| chr2:9917926 | G | A | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1272-1115G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917926 | |||||||
| chr2:9917933 | G | A | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1272-1108G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917933 | |||||||
| chr2:9917935 | A | G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1272-1106A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917935 | |||||||
| chr2:9917988 | C | T | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-1053C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917988 | |||||||
| chr2:9917990 | T | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1272-1051T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917990 | |||||||
| chr2:9917997 | G | A | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-1044G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9917997 | |||||||
| chr2:9918020 | C | G | 1 | a0002c0002t0001g0355 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1272-1021C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918020 | |||||||
| chr2:9918023 | G | A | 4 | a0003c0004t0001g0044 a0003c0004t0001g0299 a0003c0004t0001g0300 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1018G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918023 | |||||||
| chr2:9918029 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1272-1012A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918029 | |||||||
| chr2:9918067 | G | A | 44 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(41): Show |
44 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1272-974G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918067 | |||||||
| chr2:9918071 | C | CA | 7 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0002g0174 others(4): Show |
7 | HG01123.hp2 HG01175.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272-957dupA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 9918071 | ||||||
| chr2:9918188 | A | G | 1 | a0003c0004t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1272-853A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918188 | |||||||
| chr2:9918212 | T | C | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-829T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918212 | |||||||
| chr2:9918346 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1272-695T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918346 | |||||||
| chr2:9918369 | C | G | 4 | a0005c0007t0001g0073 a0010c0014t0001g0072 a0010c0014t0001g0074 others(1): Show |
4 | HG00639.hp2 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272-672C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918369 | |||||||
| chr2:9918446 | A | G | 128 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1272-595A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918446 | |||||||
| chr2:9918447 | T | C | 72 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1272-594T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918447 | |||||||
| chr2:9918454 | T | C | 77 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(74): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1272-587T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918454 | |||||||
| chr2:9918548 | C | A | 1 | a0015c0019t0001g0237 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1272-493C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918548 | |||||||
| chr2:9918608 | C | T | 125 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(122): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1272-433C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918608 | |||||||
| chr2:9918717 | A | G | 151 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(148): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1272-324A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918717 | |||||||
| chr2:9918968 | A | C | 183 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1272-73A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9918968 | |||||||
| chr2:9919008 | G | A | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1272-33G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 12/14 | chr2 | 9919008 | |||||||
| chr2:9919200 | T | G | 3 | a0009c0012t0001g0346 a0009c0012t0001g0347 a0009c0012t0001g0348 |
3 | HG00099.hp1 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1342+89T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 13/14 | chr2 | 9919200 | |||||||
| chr2:9919225 | T | C | 1 | a0005c0011t0001g0351 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1342+114T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 13/14 | chr2 | 9919225 | |||||||
| chr2:9919351 | C | T | 26 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0049 others(23): Show |
26 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1342+240C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 13/14 | chr2 | 9919351 | |||||||
| chr2:9919416 | A | G | 157 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(154): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1343-182A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 13/14 | chr2 | 9919416 | |||||||
| chr2:9919491 | G | C | 157 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(154): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1343-107G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 13/14 | chr2 | 9919491 | |||||||
| chr2:9919907 | T | A | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1565+87T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9919907 | |||||||
| chr2:9919979 | A | G | 12 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(9): Show |
12 | HG01496.hp1 HG02258.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1565+159A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9919979 | |||||||
| chr2:9920071 | G | A | 1 | a0005c0005t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1565+251G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920071 | |||||||
| chr2:9920092 | G | A | 1 | a0006c0006t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1565+272G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920092 | |||||||
| chr2:9920146 | C | G | 1 | a0002c0002t0001g0065 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1565+326C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920146 | |||||||
| chr2:9920221 | T | C | 4 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(1): Show |
4 | HG03225.hp1 HG03453.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565+401T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920221 | |||||||
| chr2:9920235 | C | T | 1 | a0001c0001t0002g0004 | 2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1565+415C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920235 | |||||||
| chr2:9920240 | T | C | 5 | a0002c0002t0001g0115 a0005c0005t0001g0033 a0006c0006t0003g0001 others(2): Show |
8 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1565+420T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920240 | |||||||
| chr2:9920282 | A | G | 9 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(6): Show |
9 | HG02965.hp1 HG03130.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565+462A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920282 | |||||||
| chr2:9920314 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1565+494A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920314 | |||||||
| chr2:9920450 | C | T | 68 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0002g0002 others(65): Show |
76 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1565+630C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920450 | |||||||
| chr2:9920458 | T | G | 79 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0002g0002 others(76): Show |
86 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1565+638T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920458 | |||||||
| chr2:9920531 | T | C | 1 | a0004c0003t0001g0239 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1565+711T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920531 | |||||||
| chr2:9920568 | G | A | 2 | a0003c0004t0001g0303 a0003c0004t0001g0308 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1565+748G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920568 | |||||||
| chr2:9920583 | G | GGGT | 16 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(13): Show |
16 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1565+765_1565+766i others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9920583 | ||||||
| chr2:9920586 | C | G | 15 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(12): Show |
15 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1565+766C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920586 | |||||||
| chr2:9920586 | C | T | 1 | a0009c0012t0001g0346 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1565+766C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920586 | |||||||
| chr2:9920708 | C | T | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+888C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920708 | |||||||
| chr2:9920822 | C | T | 12 | a0002c0002t0001g0336 a0003c0004t0001g0306 a0006c0006t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1565+1002C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920822 | |||||||
| chr2:9920851 | A | G | 236 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0198 others(233): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1565+1031A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920851 | |||||||
| chr2:9920957 | T | G | 1 | a0002c0002t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1565+1137T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9920957 | |||||||
| chr2:9921001 | C | T | 141 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(138): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1565+1181C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921001 | |||||||
| chr2:9921002 | G | A | 1 | a0003c0004t0001g0281 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1565+1182G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921002 | |||||||
| chr2:9921143 | G | A | 3 | a0006c0006t0001g0026 a0006c0006t0001g0027 a0006c0006t0001g0028 |
3 | HG02615.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1565+1323G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921143 | |||||||
| chr2:9921155 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1565+1335G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921155 | |||||||
| chr2:9921210 | G | A | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+1390G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921210 | |||||||
| chr2:9921264 | T | C | 10 | a0001c0001t0002g0174 a0001c0001t0002g0194 a0001c0001t0007g0201 others(7): Show |
10 | HG00735.hp2 HG01175.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565+1444T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921264 | |||||||
| chr2:9921272 | G | A | 75 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0002g0002 others(72): Show |
84 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1565+1452G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921272 | |||||||
| chr2:9921463 | C | T | 141 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(138): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1565+1643C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921463 | |||||||
| chr2:9921467 | C | T | 2 | a0003c0004t0001g0313 a0003c0004t0001g0314 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1565+1647C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921467 | |||||||
| chr2:9921522 | A | G | 4 | a0005c0005t0001g0013 a0005c0005t0001g0081 a0005c0005t0001g0084 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565+1702A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921522 | |||||||
| chr2:9921608 | T | A | 4 | a0010c0014t0001g0072 a0010c0014t0001g0074 a0010c0014t0001g0337 others(1): Show |
4 | HG00639.hp2 HG02976.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565+1788T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9921608 | |||||||
| chr2:9922055 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0202 |
2 | HG01123.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1565+2235A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922055 | |||||||
| chr2:9922146 | T | C | 1 | a0015c0019t0001g0237 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1565+2326T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922146 | |||||||
| chr2:9922237 | T | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+2417T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922237 | |||||||
| chr2:9922456 | A | G | 1 | a0004c0003t0001g0290 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1565+2636A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922456 | |||||||
| chr2:9922478 | C | T | 2 | a0005c0007t0001g0339 a0005c0007t0001g0340 |
2 | HG01496.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1565+2658C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922478 | |||||||
| chr2:9922524 | C | T | 141 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(138): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1565+2704C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922524 | |||||||
| chr2:9922770 | G | C | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+2950G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922770 | |||||||
| chr2:9922790 | C | A | 1 | a0001c0001t0002g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1565+2970C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922790 | |||||||
| chr2:9922974 | G | T | 3 | a0006c0006t0001g0026 a0006c0006t0001g0027 a0006c0006t0001g0028 |
3 | HG02615.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1565+3154G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9922974 | |||||||
| chr2:9923122 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1565+3302A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923122 | |||||||
| chr2:9923131 | G | A | 1 | a0005c0005t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1565+3311G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923131 | |||||||
| chr2:9923138 | T | C | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+3318T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923138 | |||||||
| chr2:9923237 | C | CA | 8 | a0003c0004t0001g0284 a0004c0003t0001g0223 a0004c0003t0001g0227 others(5): Show |
8 | HG02300.hp2 HG03041.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1565+3436dupA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9923237 | ||||||
| chr2:9923237 | CA | C | 68 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(65): Show |
68 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1565+3436delA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9923237 | ||||||
| chr2:9923237 | CAA | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0002c0002t0001g0147 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1565+3435_1565+343 others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9923237 | ||||||
| chr2:9923237 | CAAA | C | 68 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(65): Show |
77 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1565+3434_1565+343 others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9923237 | ||||||
| chr2:9923376 | CGATTAAA others(4): Show |
C | 1 | a0001c0001t0002g0203 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1565+3558_1565+356 others(15): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9923376 | ||||||
| chr2:9923407 | G | A | 3 | a0006c0006t0001g0026 a0006c0006t0001g0027 a0006c0006t0001g0028 |
3 | HG02615.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1565+3587G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923407 | |||||||
| chr2:9923487 | T | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+3667T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923487 | |||||||
| chr2:9923508 | T | A | 74 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0002g0002 others(71): Show |
83 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1565+3688T>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923508 | |||||||
| chr2:9923535 | T | C | 142 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(139): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1565+3715T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923535 | |||||||
| chr2:9923538 | A | G | 105 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0002c0002t0001g0142 others(102): Show |
107 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1565+3718A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923538 | |||||||
| chr2:9923609 | G | A | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | NA18943.hp2 NA18962.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1565+3789G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923609 | |||||||
| chr2:9923636 | G | A | 1 | a0005c0005t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1565+3816G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923636 | |||||||
| chr2:9923679 | CA | C | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+3872delA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9923679 | ||||||
| chr2:9923728 | G | A | 1 | a0006c0006t0001g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1565+3908G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923728 | |||||||
| chr2:9923778 | C | T | 1 | a0010c0014t0001g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1565+3958C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923778 | |||||||
| chr2:9923847 | C | A | 4 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565+4027C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923847 | |||||||
| chr2:9923873 | T | TC | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+4055dupC | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9923873 | ||||||
| chr2:9923943 | C | T | 1 | a0012c0013t0001g0045 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1565+4123C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923943 | |||||||
| chr2:9923944 | G | A | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1565+4124G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923944 | |||||||
| chr2:9923999 | TCA | T | 5 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0009c0012t0001g0346 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+4180_1565+418 others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9923999 | |||||||
| chr2:9924163 | A | G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1565+4343A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924163 | |||||||
| chr2:9924186 | C | A | 1 | a0001c0001t0002g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1565+4366C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924186 | |||||||
| chr2:9924195 | G | A | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+4375G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924195 | |||||||
| chr2:9924211 | A | G | 1 | a0005c0007t0001g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1565+4391A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924211 | |||||||
| chr2:9924229 | A | G | 10 | a0003c0004t0001g0302 a0003c0004t0001g0306 a0003c0004t0001g0309 others(7): Show |
10 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565+4409A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924229 | |||||||
| chr2:9924292 | C | T | 1 | a0004c0003t0001g0241 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1565+4472C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924292 | |||||||
| chr2:9924304 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1565+4484C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924304 | |||||||
| chr2:9924321 | C | A | 41 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(38): Show |
41 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1565+4501C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924321 | |||||||
| chr2:9924448 | A | G | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+4628A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924448 | |||||||
| chr2:9924495 | T | G | 4 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565+4675T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924495 | |||||||
| chr2:9924551 | G | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+4731G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924551 | |||||||
| chr2:9924587 | T | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1565+4767T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924587 | |||||||
| chr2:9924662 | G | A | 62 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1565+4842G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924662 | |||||||
| chr2:9924663 | A | T | 1 | a0001c0001t0002g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1565+4843A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924663 | |||||||
| chr2:9924720 | G | A | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+4900G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924720 | |||||||
| chr2:9924955 | A | G | 1 | a0003c0004t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1565+5135A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9924955 | |||||||
| chr2:9925205 | G | A | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+5385G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925205 | |||||||
| chr2:9925217 | G | A | 1 | a0005c0007t0001g0339 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1565+5397G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925217 | |||||||
| chr2:9925257 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1565+5437T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925257 | |||||||
| chr2:9925296 | C | T | 5 | a0003c0004t0001g0298 a0005c0007t0001g0056 a0005c0007t0001g0057 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1565+5476C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925296 | |||||||
| chr2:9925364 | C | T | 1 | a0003c0004t0001g0283 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1565+5544C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925364 | |||||||
| chr2:9925365 | G | A | 5 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0009c0012t0001g0346 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+5545G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925365 | |||||||
| chr2:9925372 | G | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+5552G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925372 | |||||||
| chr2:9925394 | T | C | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+5574T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925394 | |||||||
| chr2:9925410 | A | C | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+5590A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925410 | |||||||
| chr2:9925474 | T | C | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1565+5654T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925474 | |||||||
| chr2:9925589 | G | GT | 69 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(66): Show |
69 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1565+5779dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9925589 | ||||||
| chr2:9925589 | G | GTT | 72 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0002g0002 others(69): Show |
81 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1565+5778_1565+577 others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9925589 | ||||||
| chr2:9925701 | C | T | 1 | a0006c0006t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1565+5881C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925701 | |||||||
| chr2:9925702 | G | A | 1 | a0005c0005t0001g0108 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1565+5882G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925702 | |||||||
| chr2:9925766 | G | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+5946G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925766 | |||||||
| chr2:9925913 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | NA18964.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1565+6093G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925913 | |||||||
| chr2:9925940 | A | G | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+6120A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9925940 | |||||||
| chr2:9926050 | C | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+6230C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926050 | |||||||
| chr2:9926055 | G | A | 136 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(133): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1565+6235G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926055 | |||||||
| chr2:9926110 | C | T | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+6290C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926110 | |||||||
| chr2:9926138 | C | G | 144 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(141): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1565+6318C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926138 | |||||||
| chr2:9926205 | A | G | 1 | a0005c0011t0001g0350 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1565+6385A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926205 | |||||||
| chr2:9926488 | C | CATCTA | 6 | a0001c0001t0001g0261 a0002c0002t0001g0039 a0002c0002t0001g0040 others(3): Show |
6 | NA18946.hp1 NA18964.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1565+6670_1565+667 others(9): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9926488 | ||||||
| chr2:9926495 | C | T | 5 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0009c0012t0001g0346 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+6675C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926495 | |||||||
| chr2:9926565 | G | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1565+6745G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926565 | |||||||
| chr2:9926592 | A | C | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1565+6772A>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926592 | |||||||
| chr2:9926700 | A | G | 1 | a0005c0011t0001g0349 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1565+6880A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926700 | |||||||
| chr2:9926708 | G | A | 5 | a0001c0001t0002g0041 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | NA18971.hp2 NA18975.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1565+6888G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926708 | |||||||
| chr2:9926771 | A | G | 127 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0002g0183 others(124): Show |
129 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1565+6951A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926771 | |||||||
| chr2:9926787 | G | A | 76 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(73): Show |
78 | HG00639.hp1 HG00639.hp2 HG01109.hp2 others(75): Show |
intron_variant | MODIFIER | c.1565+6967G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926787 | |||||||
| chr2:9926804 | C | CA | 106 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0002g0002 others(103): Show |
115 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1566-6961dupA | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9926804 | ||||||
| chr2:9926804 | C | CAA | 75 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0212 others(72): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1566-6962_1566-696 others(6): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9926804 | ||||||
| chr2:9926804 | C | CAAA | 6 | a0002c0002t0001g0141 a0002c0002t0001g0146 a0002c0002t0001g0152 others(3): Show |
6 | HG01257.hp1 HG02602.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566-6963_1566-696 others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9926804 | ||||||
| chr2:9926821 | A | G | 1 | a0004c0003t0001g0265 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1566-6962A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926821 | |||||||
| chr2:9926823 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1566-6960G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9926823 | |||||||
| chr2:9927022 | G | GT | 4 | a0007c0008t0001g0229 a0007c0008t0001g0243 a0007c0008t0001g0244 others(1): Show |
4 | NA18946.hp2 NA18992.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566-6761_1566-676 others(5): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927022 | |||||||
| chr2:9927048 | G | A | 1 | a0004c0003t0001g0241 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1566-6735G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927048 | |||||||
| chr2:9927062 | G | A | 63 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(60): Show |
63 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1566-6721G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927062 | |||||||
| chr2:9927102 | T | G | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-6681T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927102 | |||||||
| chr2:9927192 | T | C | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-6591T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927192 | |||||||
| chr2:9927216 | C | T | 1 | a0002c0002t0001g0359 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1566-6567C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927216 | |||||||
| chr2:9927231 | T | G | 1 | a0004c0003t0001g0273 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1566-6552T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927231 | |||||||
| chr2:9927341 | G | T | 5 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-6442G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927341 | |||||||
| chr2:9927403 | G | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-6380G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927403 | |||||||
| chr2:9927482 | T | C | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-6301T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927482 | |||||||
| chr2:9927494 | G | A | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-6289G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927494 | |||||||
| chr2:9927521 | C | T | 3 | a0011c0010t0001g0352 a0011c0010t0001g0353 a0011c0010t0001g0354 |
3 | HG01109.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1566-6262C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927521 | |||||||
| chr2:9927545 | T | G | 3 | a0011c0010t0001g0352 a0011c0010t0001g0353 a0011c0010t0001g0354 |
3 | HG01109.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1566-6238T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927545 | |||||||
| chr2:9927593 | G | C | 62 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1566-6190G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9927593 | |||||||
| chr2:9928006 | G | T | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-5777G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928006 | |||||||
| chr2:9928044 | G | A | 62 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1566-5739G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928044 | |||||||
| chr2:9928104 | C | T | 5 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0009c0012t0001g0346 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-5679C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928104 | |||||||
| chr2:9928124 | G | C | 266 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0198 others(263): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1566-5659G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928124 | |||||||
| chr2:9928270 | TGTA | T | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-5509_1566-550 others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9928270 | ||||||
| chr2:9928342 | T | C | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-5441T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928342 | |||||||
| chr2:9928369 | A | G | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-5414A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928369 | |||||||
| chr2:9928383 | C | T | 1 | a0005c0005t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1566-5400C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928383 | |||||||
| chr2:9928437 | A | G | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-5346A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928437 | |||||||
| chr2:9928442 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-5341C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928442 | |||||||
| chr2:9928446 | A | G | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-5337A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928446 | |||||||
| chr2:9928447 | A | G | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-5336A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928447 | |||||||
| chr2:9928452 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-5331C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928452 | |||||||
| chr2:9928466 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1566-5317C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928466 | |||||||
| chr2:9928592 | T | G | 3 | a0005c0005t0001g0033 a0005c0007t0001g0339 a0005c0007t0001g0340 |
3 | HG01496.hp1 HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1566-5191T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928592 | |||||||
| chr2:9928698 | C | T | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-5085C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928698 | |||||||
| chr2:9928772 | G | A | 3 | a0003c0004t0001g0010 a0003c0004t0001g0296 a0003c0004t0001g0297 |
4 | HG01167.hp1 HG01169.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-5011G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928772 | |||||||
| chr2:9928829 | C | T | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-4954C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928829 | |||||||
| chr2:9928864 | C | G | 5 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(2): Show |
5 | HG02258.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-4919C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928864 | |||||||
| chr2:9928958 | C | T | 1 | a0001c0020t0002g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1566-4825C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9928958 | |||||||
| chr2:9929115 | A | G | 117 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0002c0002t0001g0142 others(114): Show |
119 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.1566-4668A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929115 | |||||||
| chr2:9929120 | G | C | 260 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0198 others(257): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1566-4663G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929120 | |||||||
| chr2:9929142 | T | TTTG | 5 | a0003c0004t0001g0277 a0004c0003t0001g0270 a0005c0005t0001g0103 others(2): Show |
5 | HG02083.hp2 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-4611_1566-460 others(7): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9929142 | ||||||
| chr2:9929142 | T | TTTGTTG | 7 | a0002c0002t0001g0355 a0002c0002t0001g0356 a0002c0002t0001g0357 others(4): Show |
7 | HG01496.hp1 HG02258.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1566-4614_1566-460 others(10): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9929142 | ||||||
| chr2:9929142 | T | TTTGTTGT others(2): Show |
16 | a0001c0001t0001g0156 a0002c0002t0001g0142 a0003c0004t0001g0324 others(13): Show |
16 | HG00280.hp2 HG00639.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1566-4617_1566-460 others(13): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9929142 | ||||||
| chr2:9929142 | T | TTTGTTGT others(5): Show |
76 | a0001c0001t0001g0163 a0003c0004t0001g0044 a0003c0004t0001g0253 others(73): Show |
77 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1566-4620_1566-460 others(16): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9929142 | ||||||
| chr2:9929142 | T | TTTGTTGT others(8): Show |
18 | a0003c0004t0001g0010 a0003c0004t0001g0279 a0003c0004t0001g0292 others(15): Show |
19 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1566-4623_1566-460 others(19): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9929142 | ||||||
| chr2:9929142 | T | TTTGTTGT others(11): Show |
4 | a0003c0004t0001g0319 a0003c0004t0001g0321 a0003c0004t0001g0323 others(1): Show |
4 | HG02970.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-4626_1566-460 others(22): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9929142 | ||||||
| chr2:9929189 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1566-4594C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929189 | |||||||
| chr2:9929198 | G | A | 69 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(66): Show |
69 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1566-4585G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929198 | |||||||
| chr2:9929244 | C | T | 1 | a0005c0005t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1566-4539C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929244 | |||||||
| chr2:9929269 | C | G | 5 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0009c0012t0001g0346 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-4514C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929269 | |||||||
| chr2:9929271 | A | G | 198 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0198 others(195): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1566-4512A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929271 | |||||||
| chr2:9929360 | G | A | 1 | a0003c0004t0001g0318 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1566-4423G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929360 | |||||||
| chr2:9929406 | C | T | 1 | a0007c0008t0001g0236 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1566-4377C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929406 | |||||||
| chr2:9929438 | G | A | 21 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(18): Show |
21 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1566-4345G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929438 | |||||||
| chr2:9929439 | C | T | 1 | a0002c0002t0001g0336 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1566-4344C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929439 | |||||||
| chr2:9929542 | T | G | 1 | a0001c0020t0002g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1566-4241T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929542 | |||||||
| chr2:9929718 | T | G | 5 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0009c0012t0001g0346 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-4065T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929718 | |||||||
| chr2:9929736 | G | C | 1 | a0003c0004t0001g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1566-4047G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929736 | |||||||
| chr2:9929738 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1566-4045T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929738 | |||||||
| chr2:9929777 | G | A | 2 | a0006c0006t0003g0001 a0006c0006t0003g0012 |
5 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-4006G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9929777 | |||||||
| chr2:9930091 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1566-3692C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9930091 | |||||||
| chr2:9930143 | A | AT | 138 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(135): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1566-3633dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9930143 | ||||||
| chr2:9930260 | T | G | 1 | a0001c0001t0002g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1566-3523T>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9930260 | |||||||
| chr2:9930338 | A | T | 1 | a0002c0002t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1566-3445A>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9930338 | |||||||
| chr2:9930385 | C | T | 5 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0009c0012t0001g0346 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-3398C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9930385 | |||||||
| chr2:9930414 | C | A | 74 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0002g0002 others(71): Show |
83 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1566-3369C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9930414 | |||||||
| chr2:9930572 | G | T | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-3211G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9930572 | |||||||
| chr2:9930596 | A | G | 4 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566-3187A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9930596 | |||||||
| chr2:9930696 | C | CTGATT | 20 | a0004c0003t0001g0032 a0004c0003t0001g0042 a0004c0003t0001g0224 others(17): Show |
20 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1566-3084_1566-308 others(9): Show |
TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9930696 | ||||||
| chr2:9931038 | C | CT | 6 | a0003c0004t0001g0294 a0003c0004t0001g0295 a0003c0004t0001g0303 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566-2737dupT | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 9931038 | ||||||
| chr2:9931244 | T | C | 3 | a0003c0004t0001g0327 a0003c0004t0001g0328 a0005c0007t0001g0132 |
3 | HG01361.hp1 HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1566-2539T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931244 | |||||||
| chr2:9931266 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1566-2517T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931266 | |||||||
| chr2:9931307 | G | A | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-2476G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931307 | |||||||
| chr2:9931417 | C | A | 62 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1566-2366C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931417 | |||||||
| chr2:9931417 | C | T | 81 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0002g0002 others(78): Show |
90 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1566-2366C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931417 | |||||||
| chr2:9931499 | G | A | 144 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(141): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1566-2284G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931499 | |||||||
| chr2:9931502 | T | C | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-2281T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931502 | |||||||
| chr2:9931573 | G | A | 2 | a0003c0004t0001g0296 a0003c0004t0001g0297 |
2 | HG01346.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1566-2210G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931573 | |||||||
| chr2:9931720 | G | C | 5 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-2063G>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931720 | |||||||
| chr2:9931952 | C | G | 1 | a0005c0005t0001g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1566-1831C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931952 | |||||||
| chr2:9931958 | G | A | 1 | a0005c0005t0001g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1566-1825G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931958 | |||||||
| chr2:9931985 | A | G | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-1798A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9931985 | |||||||
| chr2:9932040 | G | A | 5 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-1743G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932040 | |||||||
| chr2:9932047 | G | A | 269 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0198 others(266): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1566-1736G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932047 | |||||||
| chr2:9932063 | C | T | 1 | a0002c0002t0001g0128 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1566-1720C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932063 | |||||||
| chr2:9932175 | G | A | 1 | a0005c0005t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1566-1608G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932175 | |||||||
| chr2:9932212 | G | A | 4 | a0005c0007t0001g0056 a0005c0007t0001g0057 a0005c0007t0001g0058 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-1571G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932212 | |||||||
| chr2:9932240 | A | G | 3 | a0003c0004t0001g0310 a0003c0004t0001g0311 a0003c0004t0001g0312 |
3 | HG02622.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1566-1543A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932240 | |||||||
| chr2:9932251 | C | A | 1 | a0005c0005t0001g0077 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1566-1532C>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932251 | |||||||
| chr2:9932487 | A | G | 1 | a0005c0011t0001g0349 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1566-1296A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932487 | |||||||
| chr2:9932620 | C | T | 1 | a0005c0005t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1566-1163C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932620 | |||||||
| chr2:9932621 | G | A | 62 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1566-1162G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932621 | |||||||
| chr2:9932656 | T | C | 356 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0165 others(353): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1566-1127T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932656 | |||||||
| chr2:9932816 | A | G | 143 | a0001c0001t0001g0198 a0001c0001t0001g0202 a0001c0001t0001g0212 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1566-967A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932816 | |||||||
| chr2:9932847 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
78 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1566-936C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932847 | |||||||
| chr2:9932892 | C | T | 1 | a0005c0007t0001g0058 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1566-891C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932892 | |||||||
| chr2:9932956 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1566-827C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9932956 | |||||||
| chr2:9933079 | A | G | 1 | a0005c0005t0001g0090 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1566-704A>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933079 | |||||||
| chr2:9933154 | C | T | 6 | a0005c0011t0001g0349 a0005c0011t0001g0350 a0005c0011t0001g0351 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566-629C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933154 | |||||||
| chr2:9933167 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1566-616C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933167 | |||||||
| chr2:9933205 | T | C | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1566-578T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933205 | |||||||
| chr2:9933230 | G | A | 69 | a0003c0004t0001g0010 a0003c0004t0001g0044 a0003c0004t0001g0253 others(66): Show |
71 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(68): Show |
intron_variant | MODIFIER | c.1566-553G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933230 | |||||||
| chr2:9933338 | C | T | 3 | a0005c0007t0001g0011 a0005c0007t0001g0333 a0005c0007t0001g0334 |
4 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-445C>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933338 | |||||||
| chr2:9933344 | C | G | 19 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0048 others(16): Show |
19 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1566-439C>G | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933344 | |||||||
| chr2:9933575 | G | A | 1 | a0004c0003t0001g0332 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1566-208G>A | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933575 | |||||||
| chr2:9933683 | T | C | 1 | a0005c0005t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1566-100T>C | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933683 | |||||||
| chr2:9933719 | G | T | 1 | a0005c0011t0001g0349 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1566-64G>T | TAF1B | ENSG00000115750.17 | transcript | ENST00000263663.10 | protein_coding | 14/14 | chr2 | 9933719 |