Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8208 |
| ensemblid | ENSG00000159259.8 |
| hgncid | 1911 |
| symbol | CHAF1B |
| name | chromatin assembly factor 1 subunit B |
| refseq_nuc | NM_005441.3 |
| refseq_prot | NP_005432.1 |
| ensembl_nuc | ENST00000314103.6 |
| ensembl_prot | ENSP00000315700.4 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 36385392 |
| end | 36419015 |
| strand | + |
| ver | v1.2 |
| region | chr21:36385392-36419015 |
| region5000 | chr21:36380392-36424015 |
| regionname0 | CHAF1B_chr21_36385392_36419015 |
| regionname5000 | CHAF1B_chr21_36380392_36424015 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 559 | 324 | 83 | 64 | 122 | 8 | 45 | 94 | CHAF1B_chr21_36380392_36424015 | CHAF1B | MKVIT others(554): Show |
chr21 | 36380392 | 36424015 |
| a0002 | 0/0 | 559 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | MKVIT others(554): Show |
chr21 | 36380392 | 36424015 |
| a0003 | 0/0 | 559 | 7 | 0 | 4 | 0 | 2 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | MKVIT others(554): Show |
chr21 | 36380392 | 36424015 |
| a0004 | 0/0 | 559 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | MKVIT others(554): Show |
chr21 | 36380392 | 36424015 |
| a0005 | 0/0 | 559 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | MKVIT others(554): Show |
chr21 | 36380392 | 36424015 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1677 | 318 | 79 | 63 | 121 | 8 | 45 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 | ||
| a0001c0005 | 0/0 | 1677 | 4 | 3 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 | ||
| a0001c0007 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 | ||
| a0001c0008 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 | ||
| a0002c0002 | 0/0 | 1677 | 8 | 6 | 2 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 | ||
| a0003c0003 | 0/0 | 1677 | 7 | 0 | 4 | 0 | 2 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 | ||
| a0004c0004 | 0/0 | 1677 | 4 | 1 | 3 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 | ||
| a0005c0006 | 0/0 | 1677 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | ATGAA others(1672): Show |
chr21 | 36380392 | 36424015 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4466 | 142 | 24 | 42 | 49 | 4 | 23 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0002 | 1/1 | 4466 | 69 | 4 | 3 | 44 | 0 | 16 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0003 | 0/0 | 4467 | 16 | 14 | 1 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0004 | 0/0 | 4466 | 11 | 0 | 0 | 11 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0005 | 0/0 | 4467 | 10 | 5 | 3 | 0 | 2 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0006 | 0/0 | 4467 | 5 | 5 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0007 | 0/0 | 4467 | 7 | 1 | 0 | 6 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0008 | 0/0 | 4465 | 6 | 0 | 4 | 0 | 0 | 2 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0009 | 0/0 | 4467 | 6 | 6 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0010 | 0/0 | 4468 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4463): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0011 | 0/0 | 4467 | 4 | 0 | 4 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0014 | 0/0 | 4469 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4464): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0015 | 0/0 | 4465 | 3 | 1 | 0 | 1 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0016 | 0/0 | 4466 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0017 | 0/0 | 4465 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0018 | 0/0 | 4465 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0019 | 0/0 | 4467 | 2 | 1 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0020 | 0/0 | 4467 | 2 | 0 | 0 | 1 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0021 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0022 | 0/0 | 4465 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0023 | 0/0 | 4469 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4464): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0024 | 0/0 | 4467 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0025 | 0/0 | 4465 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0026 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0027 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0028 | 0/0 | 4468 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4463): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0030 | 0/0 | 4466 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0031 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0032 | 0/0 | 4466 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0033 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0034 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0035 | 0/0 | 4465 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0036 | 0/0 | 4465 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4460): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0037 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0038 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0039 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0040 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0041 | 0/0 | 4466 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0042 | 0/0 | 4466 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0043 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0044 | 0/0 | 4466 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0001t0045 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0001c0005t0006 | 0/0 | 4467 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0005t0029 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0007t0003 | 0/0 | 4467 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0001c0008t0001 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0002c0002t0010 | 0/0 | 4468 | 4 | 3 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4463): Show |
chr21 | 36380392 | 36424015 |
| a0002c0002t0012 | 0/0 | 4468 | 3 | 3 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4463): Show |
chr21 | 36380392 | 36424015 |
| a0002c0002t0046 | 0/0 | 4468 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4463): Show |
chr21 | 36380392 | 36424015 |
| a0003c0003t0001 | 0/0 | 4466 | 7 | 0 | 4 | 0 | 2 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4461): Show |
chr21 | 36380392 | 36424015 |
| a0004c0004t0003 | 0/0 | 4467 | 4 | 1 | 3 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| a0005c0006t0013 | 0/0 | 4467 | 3 | 2 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | GGGAA others(4462): Show |
chr21 | 36380392 | 36424015 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 1 | 2 | 5 | 0 | 2 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0003 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0002g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0008g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0011g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0011g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0011g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0011g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0014g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0014g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0015g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0015g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0016g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0016g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0016g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0017g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0017g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0018g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0018g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0019g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0019g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0020g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0020g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0021g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0022g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0023g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0024g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0025g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0026g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0027g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0028g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0030g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0031g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0032g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0033g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0034g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0035g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0036g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0037g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0038g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0039g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0040g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0041g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0042g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0043g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0044g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0001t0045g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0005t0006g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0005t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0005t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0005t0029g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0007t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0001c0008t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0002c0002t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0002c0002t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0002c0002t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0002c0002t0010g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0002c0002t0012g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0002c0002t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0002c0002t0046g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0003c0003t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0004c0004t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0004c0004t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0004c0004t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0004c0004t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0005c0006t0013g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0005c0006t0013g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| a0005c0006t0013g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0070 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0255 | EUR | FIN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00408 | hp2 | a0001 | c0001 | t0020 | g0165 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00438 | hp1 | a0001 | c0001 | t0031 | g0107 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00639 | hp2 | a0005 | c0006 | t0013 | g0308 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0063 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0299 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00741 | hp1 | a0001 | c0001 | t0016 | g0269 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01081 | hp1 | a0001 | c0001 | t0042 | g0001 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0256 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01106 | hp1 | a0001 | c0005 | t0006 | g0289 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01109 | hp1 | a0002 | c0002 | t0046 | g0148 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0304 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01167 | hp2 | a0004 | c0004 | t0003 | g0038 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01169 | hp2 | a0004 | c0004 | t0003 | g0039 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01175 | hp1 | a0002 | c0002 | t0010 | g0150 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01175 | hp2 | a0001 | c0001 | t0044 | g0258 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01243 | hp1 | a0004 | c0004 | t0003 | g0041 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0030 | AMR | PUR | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01256 | hp1 | a0001 | c0001 | t0011 | g0023 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0031 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01358 | hp2 | a0001 | c0001 | t0024 | g0285 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0057 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0292 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0005 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0293 | EUR | IBS | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01884 | hp2 | a0001 | c0001 | t0040 | g0232 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0147 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0305 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0056 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01943 | hp2 | a0001 | c0001 | t0041 | g0246 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01952 | hp2 | a0001 | c0001 | t0014 | g0139 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01978 | hp2 | a0001 | c0001 | t0011 | g0026 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0281 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02145 | hp1 | a0002 | c0002 | t0012 | g0145 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0058 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0287 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0051 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0010 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02602 | hp1 | a0001 | c0001 | t0008 | g0060 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02615 | hp1 | a0002 | c0002 | t0010 | g0141 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02622 | hp1 | a0001 | c0001 | t0028 | g0066 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02622 | hp2 | a0001 | c0007 | t0003 | g0151 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02698 | hp2 | a0001 | c0001 | t0020 | g0160 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02717 | hp1 | a0002 | c0002 | t0012 | g0009 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02717 | hp2 | a0001 | c0001 | t0027 | g0044 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02886 | hp2 | a0001 | c0001 | t0017 | g0282 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0275 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02896 | hp1 | a0001 | c0001 | t0025 | g0055 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02897 | hp2 | a0001 | c0001 | t0026 | g0054 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02922 | hp1 | a0004 | c0004 | t0003 | g0040 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02970 | hp1 | a0002 | c0002 | t0010 | g0149 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02970 | hp2 | a0001 | c0001 | t0033 | g0271 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0062 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02976 | hp2 | a0001 | c0001 | t0014 | g0137 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03017 | hp2 | a0001 | c0001 | t0035 | g0311 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0302 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0286 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03225 | hp1 | a0001 | c0001 | t0016 | g0270 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0146 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03453 | hp2 | a0001 | c0005 | t0029 | g0288 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03486 | hp1 | a0002 | c0002 | t0012 | g0009 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0050 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03491 | hp1 | a0001 | c0001 | t0032 | g0083 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0252 | AFR | ESN | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03540 | hp1 | a0001 | c0001 | t0038 | g0166 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03654 | hp2 | a0001 | c0001 | t0030 | g0113 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0059 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18906 | hp1 | a0001 | c0005 | t0006 | g0301 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18954 | hp2 | a0001 | c0001 | t0021 | g0201 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18957 | hp2 | a0001 | c0001 | t0036 | g0084 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18959 | hp2 | a0001 | c0001 | t0018 | g0115 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18960 | hp1 | a0001 | c0001 | t0045 | g0089 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18960 | hp2 | a0001 | c0001 | t0019 | g0119 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0243 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18965 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18969 | hp1 | a0001 | c0001 | t0015 | g0231 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18980 | hp1 | a0001 | c0001 | t0037 | g0247 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18988 | hp1 | a0001 | c0001 | t0043 | g0184 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18993 | hp2 | a0001 | c0008 | t0001 | g0260 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19001 | hp2 | a0001 | c0001 | t0018 | g0132 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19030 | hp2 | a0001 | c0001 | t0023 | g0138 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0291 | AFR | YRI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | ASW | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02109 | hp1 | a0001 | c0001 | t0014 | g0140 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02109 | hp2 | a0005 | c0006 | t0013 | g0306 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02486 | hp1 | a0001 | c0005 | t0006 | g0290 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | ACB | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03471 | hp1 | a0001 | c0001 | t0022 | g0312 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG06807 | hp1 | a0005 | c0006 | t0013 | g0307 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0295 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA20300 | hp1 | a0001 | c0001 | t0039 | g0250 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| NA21309 | hp2 | a0002 | c0002 | t0010 | g0144 | AFR | LWK | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0277 | REF | REF | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0170 | REF | REF | CHAF1B_chr21_36380392_36424015 | CHAF1B | chr21 | 36380392 | 36424015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:36387659 | C | T | 1 | a0003 | 7 | HG00323.hp2 HG00642.hp1 HG01099.hp2 others(4): Show |
missense_variant | MODERATE | c.188C>T | p.Ala63Val | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/14 | 325/4466 | 188/1680 | 63/559 | chr21 | 36387659 | |||
| chr21:36413066 | C | T | 1 | a0005 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.1244C>T | p.Pro415Leu | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/14 | 1381/4466 | 1244/1680 | 415/559 | chr21 | 36413066 | |||
| chr21:36415317 | A | C | 1 | a0002 | 8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
missense_variant | MODERATE | c.1516A>C | p.Lys506Gln | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/14 | 1653/4466 | 1516/1680 | 506/559 | chr21 | 36415317 | |||
| chr21:36415321 | C | T | 1 | a0004 | 4 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(1): Show |
missense_variant | MODERATE | c.1520C>T | p.Thr507Met | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/14 | 1657/4466 | 1520/1680 | 507/559 | chr21 | 36415321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:36402829 | C | T | 1 | a0001c0008 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.735C>T | p.Asp245Asp | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/14 | 872/4466 | 735/1680 | 245/559 | chr21 | 36402829 | |||
| chr21:36413259 | C | T | 1 | a0001c0005 | 4 | HG01106.hp1 HG02486.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.1437C>T | p.His479His | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/14 | 1574/4466 | 1437/1680 | 479/559 | chr21 | 36413259 | |||
| chr21:36413280 | G | A | 1 | a0001c0007 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1458G>A | p.Leu486Leu | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/14 | 1595/4466 | 1458/1680 | 486/559 | chr21 | 36413280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:36416391 | C | G | 1 | a0002c0002t0046 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 25 | chr21 | 36416391 | ||||||
| chr21:36416405 | G | C | 1 | a0001c0001t0021 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*39G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 39 | chr21 | 36416405 | ||||||
| chr21:36416487 | A | G | 1 | a0001c0001t0045 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 121 | chr21 | 36416487 | ||||||
| chr21:36416581 | C | T | 1 | a0001c0001t0044 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 215 | chr21 | 36416581 | ||||||
| chr21:36416582 | G | A | 23 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(20): Show |
76 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*216G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 216 | chr21 | 36416582 | ||||||
| chr21:36416670 | T | C | 1 | a0001c0001t0022 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 304 | chr21 | 36416670 | ||||||
| chr21:36416672 | G | A | 1 | a0001c0001t0030 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 306 | chr21 | 36416672 | ||||||
| chr21:36416979 | T | C | 1 | a0002c0002t0012 | 3 | HG02145.hp1 HG02717.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*613T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 613 | chr21 | 36416979 | ||||||
| chr21:36417024 | G | T | 5 | a0001c0001t0006 a0001c0001t0017 a0001c0001t0028 others(2): Show |
12 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*658G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 658 | chr21 | 36417024 | ||||||
| chr21:36417171 | G | A | 1 | a0001c0001t0023 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*805G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 805 | chr21 | 36417171 | ||||||
| chr21:36417186 | C | G | 2 | a0001c0001t0009 a0001c0001t0027 |
7 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*820C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 820 | chr21 | 36417186 | ||||||
| chr21:36417197 | G | A | 7 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(4): Show |
25 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*831G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 831 | chr21 | 36417197 | ||||||
| chr21:36417281 | C | CAT | 2 | a0001c0001t0014 a0001c0001t0023 |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*929_*930dupTA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 931 | INFO_REALIGN_3_PRIME | chr21 | 36417281 | |||||
| chr21:36417281 | CAT | C | 2 | a0001c0001t0017 a0001c0001t0022 |
3 | HG02886.hp2 HG03209.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*929_*930delTA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 929 | INFO_REALIGN_3_PRIME | chr21 | 36417281 | |||||
| chr21:36417320 | A | G | 2 | a0001c0001t0014 a0001c0001t0023 |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*954A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 954 | chr21 | 36417320 | ||||||
| chr21:36417321 | T | C | 1 | a0005c0006t0013 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*955T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 955 | chr21 | 36417321 | ||||||
| chr21:36417330 | T | A | 24 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(21): Show |
80 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*964T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 964 | chr21 | 36417330 | ||||||
| chr21:36417461 | C | T | 1 | a0005c0006t0013 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1095 | chr21 | 36417461 | ||||||
| chr21:36417486 | C | G | 1 | a0001c0001t0024 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1120C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1120 | chr21 | 36417486 | ||||||
| chr21:36417502 | A | G | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(43): Show |
270 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1136A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1136 | chr21 | 36417502 | ||||||
| chr21:36417541 | G | A | 1 | a0001c0001t0033 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1175 | chr21 | 36417541 | ||||||
| chr21:36417566 | A | G | 4 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0025 others(1): Show |
9 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1200A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1200 | chr21 | 36417566 | ||||||
| chr21:36417591 | A | G | 2 | a0001c0001t0016 a0001c0001t0033 |
4 | HG00741.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1225A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1225 | chr21 | 36417591 | ||||||
| chr21:36417655 | G | T | 1 | a0001c0001t0043 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1289G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1289 | chr21 | 36417655 | ||||||
| chr21:36417747 | G | A | 1 | a0001c0001t0034 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1381 | chr21 | 36417747 | ||||||
| chr21:36417833 | C | T | 1 | a0001c0001t0042 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1467C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1467 | chr21 | 36417833 | ||||||
| chr21:36418017 | A | AT | 4 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0026 others(1): Show |
11 | HG02622.hp1 HG02897.hp2 HG03098.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1664dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1665 | INFO_REALIGN_3_PRIME | chr21 | 36418017 | |||||
| chr21:36418017 | AT | A | 3 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0035 |
8 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1664delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1664 | INFO_REALIGN_3_PRIME | chr21 | 36418017 | |||||
| chr21:36418037 | C | T | 1 | a0005c0006t0013 | 3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1671C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1671 | chr21 | 36418037 | ||||||
| chr21:36418174 | C | T | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(3): Show |
22 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1808C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1808 | chr21 | 36418174 | ||||||
| chr21:36418267 | C | T | 1 | a0001c0001t0032 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1901C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1901 | chr21 | 36418267 | ||||||
| chr21:36418290 | G | A | 2 | a0001c0001t0004 a0001c0001t0036 |
12 | NA18951.hp1 NA18957.hp2 NA18963.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1924G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1924 | chr21 | 36418290 | ||||||
| chr21:36418291 | C | T | 1 | a0001c0001t0041 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 1925 | chr21 | 36418291 | ||||||
| chr21:36418450 | G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2084G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2084 | chr21 | 36418450 | ||||||
| chr21:36418451 | T | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2085T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2085 | chr21 | 36418451 | ||||||
| chr21:36418453 | A | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2087A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2087 | chr21 | 36418453 | ||||||
| chr21:36418454 | G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2088G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2088 | chr21 | 36418454 | ||||||
| chr21:36418459 | G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2093 | chr21 | 36418459 | ||||||
| chr21:36418460 | G | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2094G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2094 | chr21 | 36418460 | ||||||
| chr21:36418464 | G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2098G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2098 | chr21 | 36418464 | ||||||
| chr21:36418468 | T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2102 | chr21 | 36418468 | ||||||
| chr21:36418469 | T | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2103T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2103 | chr21 | 36418469 | ||||||
| chr21:36418471 | T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2105T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2105 | chr21 | 36418471 | ||||||
| chr21:36418479 | G | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2113G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2113 | chr21 | 36418479 | ||||||
| chr21:36418484 | G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2118 | chr21 | 36418484 | ||||||
| chr21:36418496 | A | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2130A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2130 | chr21 | 36418496 | ||||||
| chr21:36418499 | A | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2133A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2133 | chr21 | 36418499 | ||||||
| chr21:36418501 | G | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2135G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2135 | chr21 | 36418501 | ||||||
| chr21:36418502 | G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2136G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2136 | chr21 | 36418502 | ||||||
| chr21:36418507 | C | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2141C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2141 | chr21 | 36418507 | ||||||
| chr21:36418509 | T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2143 | chr21 | 36418509 | ||||||
| chr21:36418511 | T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2145T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2145 | chr21 | 36418511 | ||||||
| chr21:36418514 | T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2148T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2148 | chr21 | 36418514 | ||||||
| chr21:36418515 | T | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2149T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2149 | chr21 | 36418515 | ||||||
| chr21:36418520 | A | C | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2154A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2154 | chr21 | 36418520 | ||||||
| chr21:36418521 | G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2155G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2155 | chr21 | 36418521 | ||||||
| chr21:36418522 | C | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2156C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2156 | chr21 | 36418522 | ||||||
| chr21:36418525 | C | A | 1 | a0001c0001t0038 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2159C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2159 | chr21 | 36418525 | ||||||
| chr21:36418525 | C | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2159C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2159 | chr21 | 36418525 | ||||||
| chr21:36418526 | C | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2160C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2160 | chr21 | 36418526 | ||||||
| chr21:36418527 | T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2161T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2161 | chr21 | 36418527 | ||||||
| chr21:36418531 | T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2165 | chr21 | 36418531 | ||||||
| chr21:36418532 | C | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2166C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2166 | chr21 | 36418532 | ||||||
| chr21:36418534 | T | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2168T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2168 | chr21 | 36418534 | ||||||
| chr21:36418535 | G | A | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2169G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2169 | chr21 | 36418535 | ||||||
| chr21:36418536 | G | T | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2170G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2170 | chr21 | 36418536 | ||||||
| chr21:36418539 | A | T | 1 | a0002c0002t0046 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2173 | chr21 | 36418539 | ||||||
| chr21:36418540 | T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2174T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2174 | chr21 | 36418540 | ||||||
| chr21:36418544 | T | G | 1 | a0001c0001t0037 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2178T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2178 | chr21 | 36418544 | ||||||
| chr21:36418563 | G | C | 2 | a0001c0001t0014 a0001c0001t0023 |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2197G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2197 | chr21 | 36418563 | ||||||
| chr21:36418831 | A | C | 1 | a0001c0001t0040 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2465A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2465 | chr21 | 36418831 | ||||||
| chr21:36418848 | C | CA | 20 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(17): Show |
67 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2497dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2498 | INFO_REALIGN_3_PRIME | chr21 | 36418848 | |||||
| chr21:36418848 | C | CAA | 4 | a0001c0001t0010 a0002c0002t0010 a0002c0002t0012 others(1): Show |
9 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2496_*2497dupAA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2498 | INFO_REALIGN_3_PRIME | chr21 | 36418848 | |||||
| chr21:36418848 | CA | C | 4 | a0001c0001t0015 a0001c0001t0018 a0001c0001t0025 others(1): Show |
7 | HG00323.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2497delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2497 | INFO_REALIGN_3_PRIME | chr21 | 36418848 | |||||
| chr21:36419012 | G | A | 1 | a0001c0001t0039 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2646G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 14/14 | 2646 | chr21 | 36419012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:36385505 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-78+54G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385505 | |||||||
| chr21:36385512 | A | T | 1 | a0001c0001t0022g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-78+61A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385512 | |||||||
| chr21:36385523 | G | A | 30 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0003g0021 others(27): Show |
30 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.-78+72G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385523 | |||||||
| chr21:36385643 | C | T | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-78+192C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385643 | |||||||
| chr21:36385859 | CTGGATGT others(20): Show |
C | 1 | a0001c0001t0035g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-77-193_-77-167del others(27): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 36385859 | ||||||
| chr21:36385873 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77-187G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 1/13 | chr21 | 36385873 | |||||||
| chr21:36386270 | G | A | 1 | a0001c0001t0008g0051 | 1 | HG02293.hp1 | splice_region_variant&intron_variant | LOW | c.126+8G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386270 | |||||||
| chr21:36386677 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126+415G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386677 | |||||||
| chr21:36386717 | C | CT | 9 | a0001c0001t0001g0049 a0001c0001t0004g0310 a0001c0001t0009g0042 others(6): Show |
9 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+469dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36386717 | ||||||
| chr21:36386759 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.126+497G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386759 | |||||||
| chr21:36386801 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+539T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36386801 | |||||||
| chr21:36387010 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0034g0062 |
2 | HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.127-588G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387010 | |||||||
| chr21:36387213 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.127-385A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387213 | |||||||
| chr21:36387219 | G | GT | 30 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(27): Show |
31 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.127-375dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387219 | ||||||
| chr21:36387219 | G | GTTTTTT | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-375_127-374ins others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387219 | ||||||
| chr21:36387219 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127-375_127-374ins others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387219 | ||||||
| chr21:36387223 | TG | T | 3 | a0005c0006t0013g0306 a0005c0006t0013g0307 a0005c0006t0013g0308 |
3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.127-374delG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387223 | |||||||
| chr21:36387224 | G | GT | 12 | a0001c0001t0001g0205 a0001c0001t0001g0261 a0001c0001t0001g0263 others(9): Show |
12 | HG01243.hp1 HG01516.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-358dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387224 | ||||||
| chr21:36387224 | G | GTT | 78 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(75): Show |
86 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.127-359_127-358dup others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr21 | 36387224 | ||||||
| chr21:36387224 | G | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(39): Show |
43 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.127-374G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387224 | |||||||
| chr21:36387393 | T | A | 2 | a0003c0003t0001g0005 a0003c0003t0001g0063 |
3 | HG00642.hp1 HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.127-205T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387393 | |||||||
| chr21:36387581 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127-17T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 2/13 | chr21 | 36387581 | |||||||
| chr21:36387757 | C | G | 1 | a0001c0001t0002g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.259+27C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36387757 | |||||||
| chr21:36387820 | C | CT | 24 | a0001c0001t0001g0049 a0001c0001t0002g0272 a0001c0001t0002g0274 others(21): Show |
24 | HG00741.hp1 HG01109.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.259+105dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36387820 | ||||||
| chr21:36387820 | CTT | C | 6 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+104_259+105del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36387820 | ||||||
| chr21:36387848 | C | T | 3 | a0005c0006t0013g0306 a0005c0006t0013g0307 a0005c0006t0013g0308 |
3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.259+118C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36387848 | |||||||
| chr21:36387975 | C | T | 20 | a0001c0001t0001g0025 a0001c0001t0003g0024 a0001c0001t0003g0027 others(17): Show |
20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.259+245C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36387975 | |||||||
| chr21:36388103 | G | T | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259+373G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388103 | |||||||
| chr21:36388250 | C | G | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+520C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388250 | |||||||
| chr21:36388448 | G | T | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+718G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388448 | |||||||
| chr21:36388450 | A | C | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259+720A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388450 | |||||||
| chr21:36388468 | G | GT | 19 | a0001c0001t0001g0049 a0001c0001t0001g0257 a0001c0001t0001g0259 others(16): Show |
19 | HG00323.hp2 HG01099.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.259+758dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388468 | ||||||
| chr21:36388468 | GT | G | 16 | a0001c0001t0001g0071 a0001c0001t0002g0067 a0001c0001t0002g0068 others(13): Show |
16 | HG00323.hp1 HG00741.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.259+758delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388468 | ||||||
| chr21:36388468 | GTT | G | 38 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(35): Show |
39 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.259+757_259+758del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388468 | ||||||
| chr21:36388469 | T | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.259+739T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388469 | |||||||
| chr21:36388496 | TCTCACTG others(83): Show |
T | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | NA18981.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.259+772_259+861del others(90): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36388496 | ||||||
| chr21:36388546 | A | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(31): Show |
35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.259+816A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388546 | |||||||
| chr21:36388611 | C | T | 8 | a0001c0001t0001g0049 a0001c0001t0009g0042 a0001c0001t0009g0043 others(5): Show |
8 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+881C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388611 | |||||||
| chr21:36388694 | T | C | 86 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(83): Show |
95 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.259+964T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388694 | |||||||
| chr21:36388759 | G | A | 3 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0272 |
3 | HG02132.hp1 NA18951.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.259+1029G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388759 | |||||||
| chr21:36388762 | C | T | 19 | a0001c0001t0001g0025 a0001c0001t0003g0024 a0001c0001t0003g0027 others(16): Show |
19 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.259+1032C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388762 | |||||||
| chr21:36388800 | A | G | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1070A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388800 | |||||||
| chr21:36388901 | C | T | 1 | a0001c0001t0039g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.259+1171C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36388901 | |||||||
| chr21:36389037 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.259+1307C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389037 | |||||||
| chr21:36389066 | G | A | 193 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(190): Show |
207 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.259+1336G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389066 | |||||||
| chr21:36389068 | CGGTACCC others(22): Show |
C | 1 | a0001c0001t0007g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.259+1340_259+1368d others(31): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389068 | ||||||
| chr21:36389191 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.259+1461A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389191 | |||||||
| chr21:36389203 | G | A | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1473G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389203 | |||||||
| chr21:36389220 | A | T | 1 | a0001c0001t0004g0133 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.259+1490A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389220 | |||||||
| chr21:36389408 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1678T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389408 | |||||||
| chr21:36389474 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1744T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389474 | |||||||
| chr21:36389513 | G | A | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1783G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389513 | |||||||
| chr21:36389571 | C | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+1841C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389571 | |||||||
| chr21:36389604 | C | CA | 10 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG00597.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+1891dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389604 | ||||||
| chr21:36389604 | C | CAA | 9 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(6): Show |
9 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.259+1890_259+1891d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389604 | ||||||
| chr21:36389604 | CA | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0007g0155 others(3): Show |
6 | HG01943.hp2 HG02486.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+1891delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389604 | ||||||
| chr21:36389681 | TCTAAAGT others(10): Show |
T | 86 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(83): Show |
95 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.260-1869_260-1853d others(19): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389681 | |||||||
| chr21:36389758 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0026g0054 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.260-1793_260-1792i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389758 | |||||||
| chr21:36389758 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0025g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.260-1793_260-1792i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389758 | |||||||
| chr21:36389759 | A | ATATATGT others(3): Show |
1 | a0001c0001t0005g0302 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.260-1791_260-1790i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | A | ATG | 17 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0196 others(14): Show |
18 | HG00408.hp2 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.260-1751_260-1750d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | A | ATGTG | 16 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0164 others(13): Show |
16 | HG00408.hp1 HG01361.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.260-1753_260-1750d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | A | ATGTGTG | 3 | a0001c0001t0001g0203 a0001c0001t0001g0265 a0002c0002t0010g0150 |
3 | HG01175.hp1 NA18956.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.260-1755_260-1750d others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0169 a0001c0001t0008g0059 a0001c0001t0008g0060 |
3 | HG00642.hp2 HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.260-1757_260-1750d others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | A | G | 2 | a0001c0001t0025g0055 a0001c0001t0026g0054 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.260-1792A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389759 | |||||||
| chr21:36389759 | ATG | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0185 others(13): Show |
17 | HG00673.hp1 HG00738.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.260-1751_260-1750d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | ATGTG | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0159 others(27): Show |
31 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.260-1753_260-1750d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | ATGTGTG | A | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0191 others(5): Show |
8 | HG01123.hp1 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-1755_260-1750d others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389759 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.260-1759_260-1750d others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389759 | ||||||
| chr21:36389761 | G | A | 32 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(29): Show |
33 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.260-1790G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389761 | |||||||
| chr21:36389796 | T | C | 1 | a0001c0001t0009g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.260-1755T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389796 | |||||||
| chr21:36389796 | T | TGC | 3 | a0001c0001t0001g0049 a0001c0001t0009g0048 a0001c0001t0027g0044 |
3 | HG02280.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.260-1754_260-1753i others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389796 | ||||||
| chr21:36389798 | T | C | 15 | a0001c0001t0001g0049 a0001c0001t0001g0142 a0001c0001t0002g0074 others(12): Show |
15 | HG01952.hp2 HG02109.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-1753T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389798 | |||||||
| chr21:36389798 | T | TGC | 4 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
4 | HG00741.hp1 NA18612.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-1752_260-1751i others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | ||||||
| chr21:36389798 | T | TGCGC | 3 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0032g0083 |
3 | HG03490.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.260-1752_260-1751i others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | ||||||
| chr21:36389798 | T | TGCGCGCG others(11): Show |
2 | a0001c0001t0001g0019 a0001c0001t0007g0278 |
3 | HG03098.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.260-1752_260-1751i others(20): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | ||||||
| chr21:36389798 | T | TGCGCGCG others(13): Show |
1 | a0001c0001t0001g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-1752_260-1751i others(22): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389798 | ||||||
| chr21:36389800 | T | C | 32 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0142 others(29): Show |
33 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.260-1751T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389800 | |||||||
| chr21:36389800 | T | TGC | 9 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(6): Show |
9 | HG00323.hp2 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-1744_260-1743d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGCGC | 28 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0002g0072 others(25): Show |
28 | HG01975.hp2 HG01981.hp1 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.260-1746_260-1743d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGCGCGCG others(1): Show |
3 | a0001c0001t0003g0035 a0001c0001t0005g0302 a0001c0001t0011g0026 |
3 | HG01978.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1743d others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGCGTGCG others(3): Show |
2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.260-1748_260-1747i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGC | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0003c0003t0001g0256 |
3 | HG01099.hp2 HG01433.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGCGC | 31 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0002g0002 others(28): Show |
39 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGCGCG others(1): Show |
7 | a0001c0001t0002g0121 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGCGCG others(15): Show |
1 | a0001c0001t0006g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGCG others(1): Show |
14 | a0001c0001t0001g0061 a0001c0001t0001g0134 a0001c0001t0002g0008 others(11): Show |
15 | HG00558.hp1 HG00558.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGCG others(3): Show |
5 | a0001c0001t0002g0254 a0001c0001t0003g0021 a0001c0001t0003g0032 others(2): Show |
5 | HG01167.hp2 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGCG others(5): Show |
2 | a0004c0004t0003g0039 a0005c0006t0013g0306 |
2 | HG01169.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGCG others(11): Show |
1 | a0001c0001t0006g0280 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(20): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGCG others(13): Show |
1 | a0001c0001t0006g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(22): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGCG others(15): Show |
1 | a0001c0001t0017g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGCG others(19): Show |
1 | a0001c0001t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(28): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(3): Show |
5 | a0001c0001t0001g0152 a0001c0001t0002g0129 a0001c0001t0002g0130 others(2): Show |
5 | HG01255.hp2 HG02622.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0003g0033 a0004c0004t0003g0040 a0004c0004t0003g0041 |
3 | HG00280.hp2 HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0005g0284 a0005c0006t0013g0307 |
2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(16): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0024g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(18): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(22): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(15): Show |
1 | a0001c0001t0017g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(17): Show |
1 | a0001c0001t0006g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(5): Show |
7 | a0001c0001t0001g0010 a0001c0001t0001g0153 a0001c0001t0015g0010 others(4): Show |
7 | HG01106.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(14): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0003g0022 a0001c0001t0009g0047 |
2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(16): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(9): Show |
4 | a0001c0001t0005g0292 a0001c0001t0005g0293 a0001c0001t0005g0294 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1750_260-1749i others(18): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(16): Show |
1 | a0001c0001t0006g0291 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(25): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(17): Show |
1 | a0001c0001t0028g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(24): Show |
1 | a0001c0001t0001g0296 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(33): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0011 a0001c0001t0034g0062 |
3 | HG02280.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(16): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0005g0297 a0005c0006t0013g0308 |
2 | HG00639.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(20): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0154 |
3 | HG01257.hp1 HG01258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(18): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(25): Show |
1 | a0001c0001t0001g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.260-1750_260-1749i others(34): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(15): Show |
2 | a0001c0001t0005g0299 a0001c0001t0005g0305 |
2 | HG00733.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.260-1750_260-1749i others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(27): Show |
1 | a0001c0001t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(36): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389800 | T | TGTGTGTG others(32): Show |
1 | a0001c0001t0001g0300 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.260-1750_260-1749i others(41): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36389800 | ||||||
| chr21:36389802 | C | T | 8 | a0001c0001t0007g0243 a0001c0001t0022g0312 a0001c0001t0025g0055 others(5): Show |
8 | HG01109.hp1 HG01175.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-1749C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389802 | |||||||
| chr21:36389830 | A | G | 166 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0049 others(163): Show |
176 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.260-1721A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389830 | |||||||
| chr21:36389835 | G | A | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.260-1716G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389835 | |||||||
| chr21:36389988 | G | C | 190 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
203 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.260-1563G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36389988 | |||||||
| chr21:36390028 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0257 |
2 | NA18997.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.260-1523C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390028 | |||||||
| chr21:36390039 | G | A | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1512G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390039 | |||||||
| chr21:36390073 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0158 a0001c0001t0001g0159 others(5): Show |
9 | HG00597.hp2 HG01192.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-1478C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390073 | |||||||
| chr21:36390147 | A | G | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1404A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390147 | |||||||
| chr21:36390287 | T | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(28): Show |
32 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.260-1264T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390287 | |||||||
| chr21:36390304 | G | A | 34 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(31): Show |
35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.260-1247G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390304 | |||||||
| chr21:36390333 | C | CA | 40 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0049 others(37): Show |
41 | HG00280.hp2 HG00408.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.260-1200dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | ||||||
| chr21:36390333 | C | CAAAAG | 7 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0102 others(4): Show |
7 | HG01981.hp1 NA18940.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-1214_260-1213i others(7): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | ||||||
| chr21:36390333 | C | CAAAAGA | 75 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0135 others(72): Show |
84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.260-1214_260-1213i others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | ||||||
| chr21:36390333 | CA | C | 11 | a0001c0001t0001g0134 a0001c0001t0001g0161 a0001c0001t0001g0230 others(8): Show |
11 | HG02293.hp1 HG02630.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-1200delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36390333 | ||||||
| chr21:36390339 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.260-1212A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390339 | |||||||
| chr21:36390348 | A | G | 1 | a0001c0001t0040g0232 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.260-1203A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390348 | |||||||
| chr21:36390400 | A | G | 4 | a0001c0001t0016g0269 a0001c0001t0016g0270 a0001c0001t0016g0275 others(1): Show |
4 | HG00741.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1151A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390400 | |||||||
| chr21:36390503 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.260-1048A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390503 | |||||||
| chr21:36390524 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.260-1027A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390524 | |||||||
| chr21:36390666 | T | C | 44 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(41): Show |
45 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.260-885T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390666 | |||||||
| chr21:36390885 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.260-666G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36390885 | |||||||
| chr21:36391054 | A | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(279): Show |
309 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.260-497A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391054 | |||||||
| chr21:36391076 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-475T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391076 | |||||||
| chr21:36391109 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-442A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391109 | |||||||
| chr21:36391150 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.260-401G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391150 | |||||||
| chr21:36391262 | T | C | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.260-289T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391262 | |||||||
| chr21:36391369 | C | T | 11 | a0001c0001t0006g0065 a0001c0001t0006g0280 a0001c0001t0006g0281 others(8): Show |
11 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-182C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391369 | |||||||
| chr21:36391442 | C | T | 2 | a0001c0001t0005g0294 a0001c0001t0005g0295 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.260-109C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391442 | |||||||
| chr21:36391459 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-92G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391459 | |||||||
| chr21:36391463 | C | CA | 7 | a0001c0001t0001g0233 a0001c0001t0001g0283 a0001c0001t0002g0104 others(4): Show |
7 | HG02148.hp1 HG03098.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-71dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36391463 | ||||||
| chr21:36391463 | CA | C | 24 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0161 others(21): Show |
24 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.260-71delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 36391463 | ||||||
| chr21:36391481 | T | A | 58 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0025 others(55): Show |
60 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.260-70T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391481 | |||||||
| chr21:36391495 | C | A | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-56C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 3/13 | chr21 | 36391495 | |||||||
| chr21:36391685 | C | T | 1 | a0001c0001t0022g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.377+17C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391685 | |||||||
| chr21:36391687 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.377+19T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391687 | |||||||
| chr21:36391778 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.377+110G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391778 | |||||||
| chr21:36391831 | C | T | 1 | a0001c0001t0028g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.377+163C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36391831 | |||||||
| chr21:36391907 | A | AT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
129 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.377+269dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | ||||||
| chr21:36391907 | A | ATT | 29 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0182 others(26): Show |
29 | HG00408.hp1 HG00408.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.377+268_377+269dup others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | ||||||
| chr21:36391907 | A | ATTT | 19 | a0001c0001t0001g0222 a0001c0001t0001g0300 a0001c0001t0003g0022 others(16): Show |
19 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.377+267_377+269dup others(3): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | ||||||
| chr21:36391907 | A | ATTTT | 19 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(16): Show |
20 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.377+266_377+269dup others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | ||||||
| chr21:36391907 | A | ATTTTT | 6 | a0001c0001t0001g0298 a0001c0001t0006g0280 a0001c0001t0017g0282 others(3): Show |
6 | HG01358.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.377+265_377+269dup others(5): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | ||||||
| chr21:36391907 | AT | A | 8 | a0001c0001t0001g0013 a0001c0001t0002g0075 a0001c0001t0002g0081 others(5): Show |
9 | HG00323.hp1 HG01168.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.377+269delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36391907 | ||||||
| chr21:36392078 | C | T | 2 | a0001c0001t0025g0055 a0001c0001t0026g0054 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.377+410C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392078 | |||||||
| chr21:36392088 | G | A | 8 | a0001c0001t0001g0049 a0001c0001t0009g0042 a0001c0001t0009g0043 others(5): Show |
8 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.377+420G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392088 | |||||||
| chr21:36392152 | A | G | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.377+484A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392152 | |||||||
| chr21:36392265 | C | T | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.377+597C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392265 | |||||||
| chr21:36392308 | C | G | 82 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(79): Show |
91 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.377+640C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392308 | |||||||
| chr21:36392390 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.377+722C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392390 | |||||||
| chr21:36392402 | C | G | 7 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(4): Show |
7 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.377+734C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392402 | |||||||
| chr21:36392452 | C | CG | 19 | a0001c0001t0001g0152 a0001c0001t0001g0178 a0001c0001t0001g0185 others(16): Show |
19 | HG02109.hp2 HG02738.hp2 HG02886.hp2 others(16): Show |
intron_variant | MODIFIER | c.377+788dupG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36392452 | ||||||
| chr21:36392460 | C | T | 11 | a0001c0001t0002g0099 a0001c0001t0003g0052 a0001c0001t0008g0051 others(8): Show |
11 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.377+792C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392460 | |||||||
| chr21:36392476 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.377+808C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392476 | |||||||
| chr21:36392512 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.377+844G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392512 | |||||||
| chr21:36392512 | G | GC | 13 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0244 others(10): Show |
14 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.377+850dupC | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36392512 | ||||||
| chr21:36392513 | C | T | 1 | a0001c0001t0028g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.377+845C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392513 | |||||||
| chr21:36392526 | G | A | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+858G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392526 | |||||||
| chr21:36392529 | C | T | 1 | a0001c0001t0038g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.377+861C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392529 | |||||||
| chr21:36392542 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.377+874C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392542 | |||||||
| chr21:36392546 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.377+878C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392546 | |||||||
| chr21:36392547 | G | A | 1 | a0001c0001t0023g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377+879G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392547 | |||||||
| chr21:36392583 | C | T | 1 | a0001c0001t0040g0232 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377+915C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392583 | |||||||
| chr21:36392593 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+925T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392593 | |||||||
| chr21:36392626 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.377+958G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392626 | |||||||
| chr21:36392652 | G | A | 21 | a0001c0001t0001g0025 a0001c0001t0003g0021 a0001c0001t0003g0022 others(18): Show |
21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.377+984G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392652 | |||||||
| chr21:36392667 | C | T | 1 | a0001c0001t0007g0216 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.377+999C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392667 | |||||||
| chr21:36392733 | C | T | 21 | a0001c0001t0001g0025 a0001c0001t0003g0021 a0001c0001t0003g0022 others(18): Show |
21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.377+1065C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392733 | |||||||
| chr21:36392776 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.377+1108C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392776 | |||||||
| chr21:36392804 | C | CG | 5 | a0001c0001t0001g0244 a0001c0001t0002g0106 a0001c0001t0002g0129 others(2): Show |
5 | HG01433.hp2 HG03516.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.377+1140dupG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36392804 | ||||||
| chr21:36392861 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0117 a0001c0001t0002g0127 others(1): Show |
5 | HG02257.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.377+1193G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392861 | |||||||
| chr21:36392967 | C | G | 30 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0003g0021 others(27): Show |
30 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.377+1299C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392967 | |||||||
| chr21:36392995 | C | T | 1 | a0001c0001t0034g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.377+1327C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36392995 | |||||||
| chr21:36393013 | C | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0215 |
2 | HG00741.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.377+1345C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393013 | |||||||
| chr21:36393054 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.377+1386A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393054 | |||||||
| chr21:36393058 | G | A | 1 | a0001c0001t0009g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.377+1390G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393058 | |||||||
| chr21:36393078 | G | A | 1 | a0001c0001t0019g0119 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.377+1410G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393078 | |||||||
| chr21:36393228 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.378-1319C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393228 | |||||||
| chr21:36393263 | A | AT | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1281dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393263 | ||||||
| chr21:36393267 | C | T | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1280C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393267 | |||||||
| chr21:36393280 | G | A | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1267G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393280 | |||||||
| chr21:36393408 | C | T | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.378-1139C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393408 | |||||||
| chr21:36393446 | C | CT | 20 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0064 others(17): Show |
20 | HG00408.hp1 HG01099.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.378-1078dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393446 | ||||||
| chr21:36393446 | CT | C | 24 | a0001c0001t0001g0167 a0001c0001t0001g0186 a0001c0001t0001g0198 others(21): Show |
24 | HG00323.hp1 HG00438.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.378-1078delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393446 | ||||||
| chr21:36393446 | CTT | C | 7 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(4): Show |
7 | HG01361.hp2 HG01943.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1079_378-1078d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393446 | ||||||
| chr21:36393472 | A | G | 4 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(1): Show |
4 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-1075A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393472 | |||||||
| chr21:36393477 | G | A | 1 | a0001c0001t0033g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.378-1070G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393477 | |||||||
| chr21:36393534 | C | G | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-1013C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393534 | |||||||
| chr21:36393646 | G | GTACTGTT others(26): Show |
1 | a0001c0001t0007g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.378-900_378-899ins others(33): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36393646 | ||||||
| chr21:36393646 | G | T | 3 | a0001c0001t0006g0280 a0001c0001t0006g0281 a0001c0001t0006g0291 |
3 | HG02055.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.378-901G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393646 | |||||||
| chr21:36393653 | C | T | 1 | a0001c0001t0007g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.378-894C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393653 | |||||||
| chr21:36393659 | G | T | 1 | a0001c0001t0007g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.378-888G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393659 | |||||||
| chr21:36393733 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.378-814C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393733 | |||||||
| chr21:36393803 | T | C | 1 | a0001c0001t0009g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378-744T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393803 | |||||||
| chr21:36393837 | T | G | 166 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0049 others(163): Show |
176 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.378-710T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393837 | |||||||
| chr21:36393853 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-694T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393853 | |||||||
| chr21:36393912 | T | A | 34 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(31): Show |
35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.378-635T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393912 | |||||||
| chr21:36393968 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-579T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393968 | |||||||
| chr21:36393990 | G | C | 166 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0049 others(163): Show |
176 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.378-557G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36393990 | |||||||
| chr21:36394100 | T | C | 44 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(41): Show |
45 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.378-447T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394100 | |||||||
| chr21:36394137 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378-410C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394137 | |||||||
| chr21:36394139 | C | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-408C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394139 | |||||||
| chr21:36394207 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(53): Show |
67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.378-340G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394207 | |||||||
| chr21:36394233 | C | T | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.378-314C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394233 | |||||||
| chr21:36394297 | G | C | 3 | a0001c0001t0016g0269 a0001c0001t0016g0270 a0001c0001t0016g0275 |
3 | HG00741.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.378-250G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394297 | |||||||
| chr21:36394336 | A | T | 1 | a0001c0001t0003g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.378-211A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394336 | |||||||
| chr21:36394429 | T | TG | 86 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(83): Show |
95 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.378-117dupG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 36394429 | ||||||
| chr21:36394468 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.378-79C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394468 | |||||||
| chr21:36394479 | G | A | 7 | a0002c0002t0010g0141 a0002c0002t0010g0144 a0002c0002t0010g0149 others(4): Show |
8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-68G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 4/13 | chr21 | 36394479 | |||||||
| chr21:36394730 | C | CT | 15 | a0001c0001t0001g0176 a0001c0001t0001g0194 a0001c0001t0001g0195 others(12): Show |
15 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.481+99dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36394730 | ||||||
| chr21:36394730 | CT | C | 12 | a0001c0001t0001g0071 a0001c0001t0001g0161 a0001c0001t0001g0233 others(9): Show |
12 | HG00280.hp2 HG01169.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.481+99delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36394730 | ||||||
| chr21:36394749 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.481+99T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394749 | |||||||
| chr21:36394913 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.481+263G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394913 | |||||||
| chr21:36394920 | C | T | 2 | a0001c0001t0001g0211 a0003c0003t0001g0255 |
2 | HG00323.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.481+270C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394920 | |||||||
| chr21:36394973 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+323T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394973 | |||||||
| chr21:36394977 | C | T | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+327C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36394977 | |||||||
| chr21:36395083 | C | T | 1 | a0001c0001t0020g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.481+433C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395083 | |||||||
| chr21:36395143 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0009g0042 a0001c0001t0009g0043 others(9): Show |
12 | HG01952.hp2 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.481+493C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395143 | |||||||
| chr21:36395144 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.481+494G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395144 | |||||||
| chr21:36395154 | G | A | 1 | a0001c0001t0040g0232 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481+504G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395154 | |||||||
| chr21:36395171 | A | G | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.481+521A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395171 | |||||||
| chr21:36395294 | C | G | 3 | a0001c0001t0002g0103 a0001c0001t0002g0121 a0001c0001t0002g0131 |
3 | NA18941.hp2 NA18992.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.481+644C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395294 | |||||||
| chr21:36395764 | A | AG | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+1114_481+1115i others(3): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395764 | |||||||
| chr21:36395887 | A | C | 190 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
203 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.481+1237A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36395887 | |||||||
| chr21:36396003 | G | GT | 31 | a0001c0001t0001g0025 a0001c0001t0002g0020 a0001c0001t0003g0021 others(28): Show |
31 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.481+1364dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396003 | ||||||
| chr21:36396014 | T | C | 1 | a0001c0001t0045g0089 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.481+1364T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396014 | |||||||
| chr21:36396112 | G | A | 7 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(4): Show |
7 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-1303G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396112 | |||||||
| chr21:36396182 | A | T | 166 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0049 others(163): Show |
176 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.482-1233A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396182 | |||||||
| chr21:36396202 | G | A | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-1213G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396202 | |||||||
| chr21:36396237 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0213 a0001c0001t0001g0265 others(1): Show |
4 | HG00408.hp1 NA18940.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1178C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396237 | |||||||
| chr21:36396330 | G | A | 12 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0244 others(9): Show |
13 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.482-1085G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396330 | |||||||
| chr21:36396358 | C | CA | 60 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0134 others(57): Show |
69 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.482-1032dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | ||||||
| chr21:36396358 | C | CAAA | 6 | a0001c0001t0005g0293 a0001c0001t0005g0295 a0001c0001t0008g0056 others(3): Show |
6 | HG00639.hp2 HG01517.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-1034_482-1032d others(5): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | ||||||
| chr21:36396358 | C | CAAAA | 12 | a0001c0001t0001g0300 a0001c0001t0005g0292 a0001c0001t0005g0297 others(9): Show |
12 | HG00733.hp2 HG01109.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.482-1035_482-1032d others(6): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | ||||||
| chr21:36396358 | C | CAAAAA | 14 | a0001c0001t0001g0279 a0001c0001t0001g0283 a0001c0001t0001g0296 others(11): Show |
14 | HG01884.hp1 HG02148.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-1036_482-1032d others(7): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | ||||||
| chr21:36396358 | C | CAAAAAA | 8 | a0001c0001t0001g0019 a0001c0001t0001g0298 a0001c0001t0001g0309 others(5): Show |
9 | HG01106.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-1037_482-1032d others(8): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | ||||||
| chr21:36396358 | CA | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(28): Show |
34 | HG00323.hp2 HG00423.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.482-1032delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | ||||||
| chr21:36396358 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-1041_482-1032d others(12): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396358 | ||||||
| chr21:36396538 | C | G | 4 | a0001c0001t0001g0049 a0001c0001t0009g0043 a0001c0001t0009g0048 others(1): Show |
4 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-877C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396538 | |||||||
| chr21:36396598 | G | T | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.482-817G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396598 | |||||||
| chr21:36396603 | C | T | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-812C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396603 | |||||||
| chr21:36396653 | C | CA | 34 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(31): Show |
35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.482-752dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396653 | ||||||
| chr21:36396653 | CA | C | 10 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-752delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396653 | ||||||
| chr21:36396663 | A | G | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-752A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396663 | |||||||
| chr21:36396664 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-751G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396664 | |||||||
| chr21:36396664 | G | GA | 8 | a0001c0001t0001g0016 a0001c0001t0001g0176 a0001c0001t0001g0187 others(5): Show |
9 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-740dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396664 | ||||||
| chr21:36396684 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.482-731C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396684 | |||||||
| chr21:36396825 | C | G | 21 | a0001c0001t0001g0025 a0001c0001t0003g0021 a0001c0001t0003g0022 others(18): Show |
21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.482-590C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396825 | |||||||
| chr21:36396833 | T | C | 166 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0049 others(163): Show |
176 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.482-582T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396833 | |||||||
| chr21:36396989 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0043g0184 |
2 | NA18988.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.482-426A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36396989 | |||||||
| chr21:36396991 | TTCTCAGC others(4): Show |
T | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482-419_482-409del others(11): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36396991 | ||||||
| chr21:36397135 | C | T | 1 | a0005c0006t0013g0306 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.482-280C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397135 | |||||||
| chr21:36397233 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.482-182C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397233 | |||||||
| chr21:36397279 | A | G | 90 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(87): Show |
99 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.482-136A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397279 | |||||||
| chr21:36397292 | CT | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG00738.hp2 HG01257.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-121delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36397292 | ||||||
| chr21:36397352 | A | G | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-63A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397352 | |||||||
| chr21:36397390 | G | C | 1 | a0001c0001t0035g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.482-25G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397390 | |||||||
| chr21:36397391 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0283 a0001c0001t0003g0022 |
3 | HG02486.hp2 HG03471.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.482-24C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397391 | |||||||
| chr21:36397392 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.482-23G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397392 | |||||||
| chr21:36397402 | G | GT | 9 | a0001c0001t0001g0188 a0001c0001t0003g0268 a0001c0001t0008g0051 others(6): Show |
9 | HG00408.hp2 HG01192.hp1 HG01361.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.482-5dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 36397402 | ||||||
| chr21:36397402 | G | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
4 | HG00738.hp1 HG02738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-13G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397402 | |||||||
| chr21:36397403 | T | TG | 11 | a0001c0001t0005g0284 a0001c0001t0005g0292 a0001c0001t0005g0293 others(8): Show |
11 | HG00733.hp2 HG01109.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-12_482-11insG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 5/13 | chr21 | 36397403 | |||||||
| chr21:36397554 | A | G | 30 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0003g0021 others(27): Show |
30 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.578+43A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397554 | |||||||
| chr21:36397605 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | NA18966.hp1 NA18983.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.578+94C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397605 | |||||||
| chr21:36397719 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.578+208C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397719 | |||||||
| chr21:36397719 | C | CT | 45 | a0001c0001t0001g0019 a0001c0001t0001g0157 a0001c0001t0001g0171 others(42): Show |
46 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.578+229dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36397719 | ||||||
| chr21:36397719 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.578+208C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397719 | |||||||
| chr21:36397719 | CT | C | 13 | a0001c0001t0001g0071 a0001c0001t0001g0159 a0001c0001t0001g0162 others(10): Show |
13 | HG01070.hp1 HG01070.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.578+229delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36397719 | ||||||
| chr21:36397719 | CTTTTTTT others(4): Show |
C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.578+219_578+229del others(11): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36397719 | ||||||
| chr21:36397836 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0009g0043 a0001c0001t0009g0048 others(1): Show |
4 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+325T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397836 | |||||||
| chr21:36397929 | C | T | 15 | a0001c0001t0001g0105 a0001c0001t0002g0002 a0001c0001t0002g0074 others(12): Show |
19 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.578+418C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397929 | |||||||
| chr21:36397936 | C | G | 1 | a0001c0001t0002g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.578+425C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397936 | |||||||
| chr21:36397985 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.578+474A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36397985 | |||||||
| chr21:36398055 | AT | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
19 | HG01167.hp2 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.578+559delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36398055 | ||||||
| chr21:36398113 | T | C | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.578+602T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398113 | |||||||
| chr21:36398198 | G | A | 6 | a0001c0001t0001g0202 a0001c0001t0001g0209 a0001c0001t0001g0210 others(3): Show |
6 | HG00408.hp2 HG01978.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.578+687G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398198 | |||||||
| chr21:36398273 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.578+762C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398273 | |||||||
| chr21:36398341 | G | A | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.578+830G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398341 | |||||||
| chr21:36398609 | G | A | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-912G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398609 | |||||||
| chr21:36398712 | G | C | 166 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0049 others(163): Show |
176 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.579-809G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398712 | |||||||
| chr21:36398766 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.579-755G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398766 | |||||||
| chr21:36398772 | T | A | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-749T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36398772 | |||||||
| chr21:36399034 | C | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0203 |
2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.579-487C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399034 | |||||||
| chr21:36399036 | A | AT | 36 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0001g0180 others(33): Show |
36 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.579-467dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36399036 | ||||||
| chr21:36399036 | AT | A | 10 | a0001c0001t0001g0261 a0001c0001t0001g0300 a0001c0001t0002g0272 others(7): Show |
10 | HG00323.hp1 HG01167.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-467delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36399036 | ||||||
| chr21:36399036 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0175 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.579-476_579-467del others(10): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 36399036 | ||||||
| chr21:36399179 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.579-342C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399179 | |||||||
| chr21:36399185 | C | T | 4 | a0001c0001t0009g0042 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG03139.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-336C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399185 | |||||||
| chr21:36399216 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-305G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399216 | |||||||
| chr21:36399282 | C | A | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-239C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399282 | |||||||
| chr21:36399288 | T | C | 96 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(93): Show |
105 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.579-233T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399288 | |||||||
| chr21:36399303 | C | T | 1 | a0001c0001t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.579-218C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399303 | |||||||
| chr21:36399328 | G | A | 19 | a0001c0001t0001g0025 a0001c0001t0003g0024 a0001c0001t0003g0027 others(16): Show |
19 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.579-193G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399328 | |||||||
| chr21:36399397 | T | C | 22 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(19): Show |
23 | HG01106.hp1 HG01167.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.579-124T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399397 | |||||||
| chr21:36399507 | T | C | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.579-14T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 6/13 | chr21 | 36399507 | |||||||
| chr21:36399706 | A | G | 10 | a0001c0001t0003g0052 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.663+101A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36399706 | |||||||
| chr21:36399848 | C | G | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.663+243C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36399848 | |||||||
| chr21:36399991 | C | A | 1 | a0001c0001t0002g0020 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.663+386C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36399991 | |||||||
| chr21:36400128 | G | A | 1 | a0002c0002t0012g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.663+523G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400128 | |||||||
| chr21:36400262 | C | G | 3 | a0004c0004t0003g0038 a0004c0004t0003g0039 a0004c0004t0003g0041 |
3 | HG01167.hp2 HG01169.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.663+657C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400262 | |||||||
| chr21:36400292 | C | G | 81 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(78): Show |
90 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.663+687C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400292 | |||||||
| chr21:36400348 | G | A | 19 | a0001c0001t0001g0025 a0001c0001t0003g0024 a0001c0001t0003g0027 others(16): Show |
19 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.663+743G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400348 | |||||||
| chr21:36400394 | C | T | 8 | a0001c0001t0001g0049 a0001c0001t0009g0042 a0001c0001t0009g0043 others(5): Show |
8 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.663+789C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400394 | |||||||
| chr21:36400421 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.663+816A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400421 | |||||||
| chr21:36400457 | G | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(17): Show |
21 | HG01106.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.663+852G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400457 | |||||||
| chr21:36400540 | C | T | 81 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(78): Show |
90 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.663+935C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400540 | |||||||
| chr21:36400630 | C | T | 1 | a0001c0001t0003g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.663+1025C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400630 | |||||||
| chr21:36400658 | C | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(31): Show |
35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.663+1053C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400658 | |||||||
| chr21:36400668 | G | C | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.663+1063G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400668 | |||||||
| chr21:36400690 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.663+1085A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400690 | |||||||
| chr21:36400700 | G | T | 7 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+1095G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400700 | |||||||
| chr21:36400824 | C | A | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.663+1219C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400824 | |||||||
| chr21:36400833 | C | T | 1 | a0001c0001t0045g0089 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.663+1228C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400833 | |||||||
| chr21:36400866 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.663+1261G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400866 | |||||||
| chr21:36400958 | A | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(31): Show |
35 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.663+1353A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400958 | |||||||
| chr21:36400990 | G | A | 2 | a0001c0001t0025g0055 a0001c0001t0026g0054 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.663+1385G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400990 | |||||||
| chr21:36400996 | G | A | 1 | a0001c0001t0009g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.663+1391G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36400996 | |||||||
| chr21:36401322 | T | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.664-1436T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401322 | |||||||
| chr21:36401349 | T | C | 1 | a0005c0006t0013g0306 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.664-1409T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401349 | |||||||
| chr21:36401352 | A | AATATATA others(17): Show |
1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.664-1400_664-1399i others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | ||||||
| chr21:36401352 | A | AATATATT others(17): Show |
10 | a0001c0001t0001g0016 a0001c0001t0001g0187 a0001c0001t0001g0188 others(7): Show |
11 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-1180_664-1157d others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | ||||||
| chr21:36401352 | A | AATATATT others(41): Show |
1 | a0001c0001t0001g0210 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.664-1204_664-1157d others(50): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | ||||||
| chr21:36401352 | AATATATT others(17): Show |
A | 8 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0001g0173 others(5): Show |
8 | HG00673.hp1 HG01981.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-1180_664-1157d others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | ||||||
| chr21:36401352 | AATATATT others(41): Show |
A | 1 | a0001c0001t0001g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.664-1204_664-1157d others(50): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401352 | ||||||
| chr21:36401371 | C | T | 39 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0003g0021 others(36): Show |
39 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.664-1387C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401371 | |||||||
| chr21:36401400 | T | TATATATT others(15): Show |
1 | a0001c0001t0002g0081 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.664-1351_664-1330d others(24): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401400 | ||||||
| chr21:36401422 | AAT | A | 80 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(77): Show |
89 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.664-1329_664-1328d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401422 | ||||||
| chr21:36401521 | A | G | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-1237A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401521 | |||||||
| chr21:36401525 | AT | A | 22 | a0001c0001t0001g0296 a0001c0001t0005g0284 a0001c0001t0005g0294 others(19): Show |
22 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.664-1228delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401525 | ||||||
| chr21:36401549 | AT | A | 48 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0279 others(45): Show |
49 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.664-1204delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401549 | ||||||
| chr21:36401549 | ATTTTTAT others(18): Show |
A | 14 | a0001c0001t0005g0284 a0001c0001t0005g0294 a0001c0001t0005g0295 others(11): Show |
14 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.664-1204_664-1180d others(27): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401549 | ||||||
| chr21:36401550 | T | TTTTTATA others(16): Show |
1 | a0001c0001t0023g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.664-1203_664-1181d others(25): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401550 | ||||||
| chr21:36401550 | TTTTTATA others(40): Show |
T | 7 | a0001c0001t0009g0042 a0001c0001t0009g0045 a0001c0001t0009g0046 others(4): Show |
7 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1171_664-1125d others(49): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401550 | ||||||
| chr21:36401573 | AT | A | 123 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(120): Show |
135 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.664-1180delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401573 | ||||||
| chr21:36401574 | T | TTTTATAT others(39): Show |
1 | a0002c0002t0010g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664-1181_664-1180i others(48): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401574 | ||||||
| chr21:36401574 | TTTTTATA others(16): Show |
T | 29 | a0001c0001t0001g0025 a0001c0001t0001g0303 a0001c0001t0003g0021 others(26): Show |
29 | HG00280.hp2 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.664-1156_664-1134d others(25): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401574 | ||||||
| chr21:36401597 | A | AT | 106 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(103): Show |
117 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.664-1157dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401597 | ||||||
| chr21:36401597 | A | ATTTTATA others(17): Show |
17 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0244 others(14): Show |
18 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.664-1148_664-1125d others(26): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401597 | ||||||
| chr21:36401597 | A | ATTTTTAT others(41): Show |
4 | a0002c0002t0010g0141 a0002c0002t0010g0149 a0002c0002t0010g0150 others(1): Show |
5 | HG01123.hp2 HG01175.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1157_664-1156i others(50): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 36401597 | ||||||
| chr21:36401634 | T | C | 8 | a0001c0001t0006g0065 a0001c0001t0008g0051 a0001c0001t0008g0056 others(5): Show |
8 | HG00639.hp2 HG01361.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-1124T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401634 | |||||||
| chr21:36401806 | T | C | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-952T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401806 | |||||||
| chr21:36401984 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.664-774G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401984 | |||||||
| chr21:36401996 | C | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-762C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36401996 | |||||||
| chr21:36402085 | G | T | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.664-673G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402085 | |||||||
| chr21:36402090 | A | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0161 a0001c0001t0001g0187 others(10): Show |
14 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.664-668A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402090 | |||||||
| chr21:36402102 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.664-656T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402102 | |||||||
| chr21:36402383 | C | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-375C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402383 | |||||||
| chr21:36402459 | A | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-299A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402459 | |||||||
| chr21:36402506 | C | T | 21 | a0001c0001t0001g0025 a0001c0001t0003g0021 a0001c0001t0003g0022 others(18): Show |
21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.664-252C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402506 | |||||||
| chr21:36402619 | A | G | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-139A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402619 | |||||||
| chr21:36402628 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.664-130A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402628 | |||||||
| chr21:36402629 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.664-129G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402629 | |||||||
| chr21:36402686 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.664-72G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402686 | |||||||
| chr21:36402725 | A | C | 1 | a0001c0001t0003g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.664-33A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 7/13 | chr21 | 36402725 | |||||||
| chr21:36402978 | T | C | 82 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0134 others(79): Show |
91 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.757+127T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36402978 | |||||||
| chr21:36403126 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.757+275G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403126 | |||||||
| chr21:36403289 | C | G | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.757+438C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403289 | |||||||
| chr21:36403359 | C | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(302): Show |
337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.757+508C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403359 | |||||||
| chr21:36403436 | GACAGAGT others(3838): Show |
G | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.757+595_758-1471de others(1): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403436 | ||||||
| chr21:36403455 | T | TA | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(30): Show |
36 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.757+629dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | ||||||
| chr21:36403455 | TA | T | 28 | a0001c0001t0001g0025 a0001c0001t0001g0071 a0001c0001t0001g0205 others(25): Show |
28 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.757+629delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | ||||||
| chr21:36403455 | TAA | T | 17 | a0001c0001t0003g0029 a0001c0001t0007g0278 a0001c0001t0009g0042 others(14): Show |
17 | HG00741.hp1 HG02109.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.757+628_757+629del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | ||||||
| chr21:36403455 | TAAA | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0283 others(30): Show |
34 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.757+627_757+629del others(3): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | ||||||
| chr21:36403455 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0207 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.757+617_757+629del others(13): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36403455 | ||||||
| chr21:36403549 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.757+698G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403549 | |||||||
| chr21:36403551 | G | A | 7 | a0001c0001t0001g0191 a0001c0001t0003g0032 a0001c0001t0003g0033 others(4): Show |
7 | HG00280.hp2 HG01243.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+700G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403551 | |||||||
| chr21:36403861 | G | A | 1 | a0001c0001t0024g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.757+1010G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403861 | |||||||
| chr21:36403903 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0002g0123 |
2 | HG00558.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.757+1052T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403903 | |||||||
| chr21:36403986 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.757+1135C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36403986 | |||||||
| chr21:36404096 | C | CT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0237 others(38): Show |
41 | HG00438.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.757+1265dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404096 | ||||||
| chr21:36404096 | CT | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0002g0006 others(12): Show |
15 | HG01361.hp2 HG01943.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.757+1265delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404096 | ||||||
| chr21:36404160 | C | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0020g0160 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.757+1309C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404160 | |||||||
| chr21:36404203 | C | T | 3 | a0001c0001t0003g0024 a0001c0001t0003g0029 a0001c0001t0003g0034 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.757+1352C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404203 | |||||||
| chr21:36404290 | G | C | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.757+1439G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404290 | |||||||
| chr21:36404399 | C | CT | 21 | a0001c0001t0003g0052 a0001c0001t0003g0192 a0001c0001t0005g0284 others(18): Show |
21 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.757+1561dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404399 | ||||||
| chr21:36404412 | T | A | 2 | a0001c0001t0031g0107 a0003c0003t0001g0005 |
2 | HG00438.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.757+1561T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404412 | |||||||
| chr21:36404413 | A | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.757+1562A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404413 | |||||||
| chr21:36404464 | C | T | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.757+1613C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404464 | |||||||
| chr21:36404503 | C | T | 13 | a0001c0001t0001g0049 a0001c0001t0001g0238 a0001c0001t0001g0239 others(10): Show |
14 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.757+1652C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404503 | |||||||
| chr21:36404558 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.757+1707C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404558 | |||||||
| chr21:36404559 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0034g0062 |
2 | HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.757+1708G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404559 | |||||||
| chr21:36404732 | C | CT | 6 | a0001c0001t0002g0088 a0001c0001t0002g0102 a0001c0001t0014g0139 others(3): Show |
6 | HG00741.hp1 HG01952.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+1908dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | ||||||
| chr21:36404732 | CT | C | 52 | a0001c0001t0001g0014 a0001c0001t0001g0157 a0001c0001t0001g0182 others(49): Show |
60 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.757+1908delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | ||||||
| chr21:36404732 | CTT | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(187): Show |
209 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.757+1907_757+1908d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | ||||||
| chr21:36404732 | CTTT | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0049 others(32): Show |
36 | HG00280.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.757+1906_757+1908d others(5): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36404732 | ||||||
| chr21:36404757 | T | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0118 |
3 | HG02080.hp1 NA18979.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.757+1906T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404757 | |||||||
| chr21:36404759 | T | A | 1 | a0001c0001t0003g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.757+1908T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404759 | |||||||
| chr21:36404927 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0182 |
4 | HG03491.hp2 HG03492.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.757+2076A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404927 | |||||||
| chr21:36404941 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.757+2090G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404941 | |||||||
| chr21:36404982 | G | A | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.757+2131G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36404982 | |||||||
| chr21:36405042 | CGCCCA | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(159): Show |
184 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.757+2196_757+2200d others(7): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36405042 | ||||||
| chr21:36405043 | G | A | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.757+2192G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405043 | |||||||
| chr21:36405113 | A | G | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.757+2262A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405113 | |||||||
| chr21:36405327 | A | G | 12 | a0001c0001t0006g0065 a0001c0001t0006g0280 a0001c0001t0006g0281 others(9): Show |
12 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.757+2476A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405327 | |||||||
| chr21:36405525 | G | T | 1 | a0003c0003t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.757+2674G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405525 | |||||||
| chr21:36405560 | G | A | 1 | a0001c0001t0038g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.757+2709G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405560 | |||||||
| chr21:36405766 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.757+2915A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405766 | |||||||
| chr21:36405929 | A | G | 10 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0009g0042 others(7): Show |
10 | HG02559.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.758-2832A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405929 | |||||||
| chr21:36405942 | T | C | 1 | a0002c0002t0046g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.758-2819T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405942 | |||||||
| chr21:36405957 | T | TA | 27 | a0001c0001t0005g0284 a0001c0001t0005g0292 a0001c0001t0005g0293 others(24): Show |
27 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.758-2794dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36405957 | ||||||
| chr21:36405984 | G | C | 1 | a0001c0001t0001g0249 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.758-2777G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36405984 | |||||||
| chr21:36406112 | T | C | 3 | a0005c0006t0013g0306 a0005c0006t0013g0307 a0005c0006t0013g0308 |
3 | HG00639.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.758-2649T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406112 | |||||||
| chr21:36406388 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(165): Show |
190 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.758-2373T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406388 | |||||||
| chr21:36406532 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(163): Show |
188 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.758-2229C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406532 | |||||||
| chr21:36406628 | G | A | 1 | a0001c0001t0003g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.758-2133G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36406628 | |||||||
| chr21:36407080 | T | C | 23 | a0001c0001t0005g0284 a0001c0001t0005g0292 a0001c0001t0005g0293 others(20): Show |
23 | HG00733.hp2 HG01106.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.758-1681T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407080 | |||||||
| chr21:36407192 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(135): Show |
157 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.758-1569C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407192 | |||||||
| chr21:36407285 | G | A | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.758-1476G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407285 | |||||||
| chr21:36407288 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1473T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407288 | |||||||
| chr21:36407289 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1472G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407289 | |||||||
| chr21:36407296 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1465T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407296 | |||||||
| chr21:36407297 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1464G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407297 | |||||||
| chr21:36407300 | T | TA | 8 | a0001c0001t0001g0210 a0001c0001t0001g0265 a0001c0001t0002g0072 others(5): Show |
8 | HG02132.hp1 HG02293.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-1444dupA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36407300 | ||||||
| chr21:36407300 | TA | T | 53 | a0001c0001t0001g0071 a0001c0001t0001g0174 a0001c0001t0002g0069 others(50): Show |
53 | HG00280.hp2 HG00733.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.758-1444delA | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr21 | 36407300 | ||||||
| chr21:36407301 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.758-1460A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407301 | |||||||
| chr21:36407317 | A | T | 3 | a0001c0001t0009g0043 a0001c0001t0009g0048 a0001c0001t0027g0044 |
3 | HG02717.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.758-1444A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407317 | |||||||
| chr21:36407317 | AG | A | 7 | a0002c0002t0010g0141 a0002c0002t0010g0144 a0002c0002t0010g0149 others(4): Show |
8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-1443delG | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407317 | |||||||
| chr21:36407418 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.758-1343C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407418 | |||||||
| chr21:36407850 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(179): Show |
204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.758-911T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36407850 | |||||||
| chr21:36408344 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.758-417A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408344 | |||||||
| chr21:36408453 | G | C | 1 | a0001c0001t0007g0216 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.758-308G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408453 | |||||||
| chr21:36408524 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(166): Show |
191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.758-237C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408524 | |||||||
| chr21:36408580 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.758-181G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408580 | |||||||
| chr21:36408677 | C | G | 2 | a0001c0001t0006g0281 a0001c0001t0006g0291 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.758-84C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408677 | |||||||
| chr21:36408748 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0008 others(38): Show |
48 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.758-13C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 8/13 | chr21 | 36408748 | |||||||
| chr21:36408885 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.827+55G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36408885 | |||||||
| chr21:36408948 | G | A | 2 | a0001c0001t0005g0297 a0001c0001t0005g0302 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.827+118G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36408948 | |||||||
| chr21:36409033 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.827+203T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409033 | |||||||
| chr21:36409046 | G | C | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+216G>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409046 | |||||||
| chr21:36409109 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.828-265C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409109 | |||||||
| chr21:36409158 | A | AT | 42 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0002g0091 others(39): Show |
42 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.828-194dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr21 | 36409158 | ||||||
| chr21:36409158 | A | ATT | 21 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0027 others(18): Show |
21 | HG00280.hp2 HG01106.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.828-195_828-194dup others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr21 | 36409158 | ||||||
| chr21:36409213 | C | A | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.828-161C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 9/13 | chr21 | 36409213 | |||||||
| chr21:36409694 | C | T | 1 | a0001c0001t0009g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.919+229C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409694 | |||||||
| chr21:36409788 | G | A | 1 | a0003c0003t0001g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.919+323G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409788 | |||||||
| chr21:36409793 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
7 | HG02074.hp1 HG02698.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+328C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409793 | |||||||
| chr21:36409836 | G | A | 4 | a0001c0001t0009g0042 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG03139.hp1 HG03516.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+371G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409836 | |||||||
| chr21:36409859 | T | G | 2 | a0001c0001t0003g0052 a0001c0001t0003g0192 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.919+394T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409859 | |||||||
| chr21:36409867 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.919+402T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409867 | |||||||
| chr21:36409884 | A | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.919+419A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409884 | |||||||
| chr21:36409921 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0236 |
3 | HG02148.hp1 HG03688.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.919+456G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36409921 | |||||||
| chr21:36409967 | C | CT | 10 | a0001c0001t0003g0267 a0001c0001t0008g0051 a0001c0001t0008g0056 others(7): Show |
10 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+516dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36409967 | ||||||
| chr21:36409967 | CT | C | 6 | a0001c0001t0001g0220 a0001c0001t0001g0245 a0001c0001t0002g0126 others(3): Show |
6 | HG00408.hp2 HG02698.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+516delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36409967 | ||||||
| chr21:36410002 | C | T | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.919+537C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410002 | |||||||
| chr21:36410045 | A | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(243): Show |
269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.919+580A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410045 | |||||||
| chr21:36410182 | C | T | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.919+717C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410182 | |||||||
| chr21:36410198 | G | T | 20 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0024 others(17): Show |
20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+733G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410198 | |||||||
| chr21:36410628 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0187 a0001c0001t0001g0188 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-835A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410628 | |||||||
| chr21:36410674 | C | CT | 20 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0024 others(17): Show |
20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-775dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36410674 | ||||||
| chr21:36410674 | CT | C | 6 | a0001c0001t0002g0131 a0002c0002t0010g0141 a0002c0002t0010g0144 others(3): Show |
6 | HG01109.hp1 HG01175.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-775delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36410674 | ||||||
| chr21:36410722 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.920-741A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410722 | |||||||
| chr21:36410729 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0190 others(8): Show |
12 | HG01167.hp1 HG01884.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.920-734C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410729 | |||||||
| chr21:36410747 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0196 a0001c0001t0001g0215 |
3 | HG00741.hp2 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.920-716G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410747 | |||||||
| chr21:36410908 | G | A | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.920-555G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36410908 | |||||||
| chr21:36411116 | CT | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(231): Show |
257 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.920-332delT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36411116 | ||||||
| chr21:36411116 | CTT | C | 10 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-333_920-332del others(2): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 36411116 | ||||||
| chr21:36411199 | C | T | 1 | a0001c0001t0008g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.920-264C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36411199 | |||||||
| chr21:36411361 | G | A | 3 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0031g0107 |
3 | HG00438.hp1 HG00558.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.920-102G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36411361 | |||||||
| chr21:36411400 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.920-63C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 10/13 | chr21 | 36411400 | |||||||
| chr21:36411614 | T | G | 12 | a0001c0001t0006g0065 a0001c0001t0006g0280 a0001c0001t0006g0281 others(9): Show |
12 | HG01106.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1061+10T>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411614 | |||||||
| chr21:36411739 | A | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0227 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1061+135A>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411739 | |||||||
| chr21:36411761 | C | T | 1 | a0001c0001t0011g0026 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1061+157C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411761 | |||||||
| chr21:36411772 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(179): Show |
204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1061+168G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411772 | |||||||
| chr21:36411803 | A | C | 7 | a0002c0002t0010g0141 a0002c0002t0010g0144 a0002c0002t0010g0149 others(4): Show |
8 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+199A>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411803 | |||||||
| chr21:36411877 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0265 |
2 | NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1061+273C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411877 | |||||||
| chr21:36411966 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0035g0311 |
2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1061+362G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36411966 | |||||||
| chr21:36412020 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1061+416G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412020 | |||||||
| chr21:36412069 | C | T | 1 | a0001c0007t0003g0151 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1061+465C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412069 | |||||||
| chr21:36412137 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1061+533C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412137 | |||||||
| chr21:36412256 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1062-628G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412256 | |||||||
| chr21:36412342 | C | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(8): Show |
13 | HG01257.hp1 HG01258.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1062-542C>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412342 | |||||||
| chr21:36412369 | G | GT | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0006g0291 others(3): Show |
6 | HG01257.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1062-505dupT | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr21 | 36412369 | ||||||
| chr21:36412384 | CAG | C | 2 | a0002c0002t0012g0009 a0002c0002t0012g0145 |
3 | HG02145.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1062-497_1062-496d others(4): Show |
CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr21 | 36412384 | ||||||
| chr21:36412422 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1062-462C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412422 | |||||||
| chr21:36412426 | C | T | 7 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(4): Show |
7 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1062-458C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412426 | |||||||
| chr21:36412445 | C | T | 5 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0003g0267 others(2): Show |
5 | HG00438.hp1 HG00558.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062-439C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412445 | |||||||
| chr21:36412494 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1062-390G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412494 | |||||||
| chr21:36412504 | C | T | 2 | a0002c0002t0012g0009 a0002c0002t0012g0145 |
3 | HG02145.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1062-380C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412504 | |||||||
| chr21:36412508 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1062-376C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 11/13 | chr21 | 36412508 | |||||||
| chr21:36413374 | C | A | 1 | a0001c0001t0007g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1493+59C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413374 | |||||||
| chr21:36413501 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1493+186A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413501 | |||||||
| chr21:36413685 | T | C | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1493+370T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413685 | |||||||
| chr21:36413696 | G | A | 2 | a0001c0001t0003g0052 a0001c0001t0003g0192 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1493+381G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413696 | |||||||
| chr21:36413706 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(212): Show |
238 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1493+391C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413706 | |||||||
| chr21:36413978 | G | A | 6 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0002g0109 others(3): Show |
6 | NA18941.hp2 NA18957.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1493+663G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36413978 | |||||||
| chr21:36414034 | G | A | 7 | a0001c0001t0009g0042 a0001c0001t0009g0043 a0001c0001t0009g0045 others(4): Show |
7 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1493+719G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414034 | |||||||
| chr21:36414050 | C | T | 4 | a0001c0001t0016g0269 a0001c0001t0016g0270 a0001c0001t0016g0275 others(1): Show |
4 | HG00741.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1493+735C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414050 | |||||||
| chr21:36414068 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0203 |
2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1493+753G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414068 | |||||||
| chr21:36414175 | C | T | 1 | a0001c0001t0024g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1493+860C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414175 | |||||||
| chr21:36414220 | C | T | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1493+905C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414220 | |||||||
| chr21:36414231 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1493+916C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414231 | |||||||
| chr21:36414312 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1494-983C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414312 | |||||||
| chr21:36414379 | G | T | 18 | a0001c0001t0003g0024 a0001c0001t0003g0027 a0001c0001t0003g0028 others(15): Show |
18 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1494-916G>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414379 | |||||||
| chr21:36414451 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1494-844T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414451 | |||||||
| chr21:36414470 | C | T | 4 | a0001c0001t0014g0137 a0001c0001t0014g0139 a0001c0001t0014g0140 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494-825C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414470 | |||||||
| chr21:36414642 | T | A | 20 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0024 others(17): Show |
20 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1494-653T>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414642 | |||||||
| chr21:36414654 | C | A | 3 | a0001c0001t0003g0024 a0001c0001t0003g0029 a0001c0001t0003g0034 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1494-641C>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414654 | |||||||
| chr21:36414719 | C | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494-576C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414719 | |||||||
| chr21:36414765 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0015g0070 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1494-530C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414765 | |||||||
| chr21:36414869 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(6): Show |
11 | HG01257.hp1 HG01258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1494-426C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414869 | |||||||
| chr21:36414899 | C | T | 3 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0007t0003g0151 |
3 | HG02559.hp2 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1494-396C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414899 | |||||||
| chr21:36414972 | C | T | 1 | a0001c0001t0024g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1494-323C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414972 | |||||||
| chr21:36414975 | T | C | 1 | a0001c0001t0006g0287 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1494-320T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36414975 | |||||||
| chr21:36415022 | C | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0056 a0001c0001t0008g0057 others(3): Show |
6 | HG01361.hp2 HG01943.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494-273C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36415022 | |||||||
| chr21:36415057 | G | A | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1494-238G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36415057 | |||||||
| chr21:36415147 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1494-148A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 12/13 | chr21 | 36415147 | |||||||
| chr21:36415493 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1588+104G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415493 | |||||||
| chr21:36415515 | C | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1588+126C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415515 | |||||||
| chr21:36415705 | T | C | 1 | a0001c0001t0007g0143 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1588+316T>C | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415705 | |||||||
| chr21:36415792 | G | A | 1 | a0001c0008t0001g0260 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1588+403G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36415792 | |||||||
| chr21:36416001 | G | A | 1 | a0001c0001t0010g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1589-274G>A | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36416001 | |||||||
| chr21:36416049 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1589-226C>T | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36416049 | |||||||
| chr21:36416239 | A | G | 3 | a0001c0001t0022g0312 a0001c0001t0025g0055 a0001c0001t0026g0054 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1589-36A>G | CHAF1B | ENSG00000159259.8 | transcript | ENST00000314103.6 | protein_coding | 13/13 | chr21 | 36416239 |