Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23774 |
|---|---|
| ensemblid | ENSG00000100425.19 |
| hgncid | 1102 |
| symbol | BRD1 |
| name | bromodomain containing 1 |
| refseq_nuc | NM_001304808.3 |
| refseq_prot | NP_001291737.1 |
| ensembl_nuc | ENST00000404760.6 |
| ensembl_prot | ENSP00000385858.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 49773283 |
| end | 49827873 |
| strand | - |
| ver | v1.2 |
| region | chr22:49773283-49827873 |
| region5000 | chr22:49768283-49832873 |
| regionname0 | BRD1_chr22_49773283_49827873 |
| regionname5000 | BRD1_chr22_49768283_49832873 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1189 | 229 | 70 | 32 | 91 | 8 | 26 | 69 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0002 | 0/0 | 1189 | 22 | 10 | 3 | 0 | 4 | 5 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0003 | 0/0 | 1189 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0004 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0005 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0006 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0007 | 0/0 | 1189 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3570 | 161 | 36 | 27 | 69 | 8 | 19 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0002 | 0/0 | 3570 | 34 | 10 | 1 | 19 | 0 | 4 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0003 | 0/0 | 3570 | 21 | 9 | 3 | 0 | 4 | 5 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0004 | 0/0 | 3570 | 12 | 8 | 1 | 2 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0005 | 0/0 | 3570 | 10 | 10 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0006 | 0/0 | 3570 | 5 | 3 | 0 | 0 | 0 | 2 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0007 | 0/0 | 3570 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0008 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0009 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0010 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0011 | 0/0 | 3570 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0012 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0013 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0014 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0015 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0016 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0017 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0018 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| c0019 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1342 | 119 | 50 | 11 | 39 | 1 | 18 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0002 | 1/1 | 1342 | 98 | 18 | 20 | 43 | 7 | 8 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0003 | 0/0 | 1342 | 22 | 10 | 3 | 0 | 4 | 5 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0004 | 0/0 | 1348 | 4 | 0 | 0 | 4 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0005 | 0/0 | 1342 | 4 | 0 | 0 | 4 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0006 | 0/0 | 1330 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0007 | 0/0 | 1342 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0008 | 0/0 | 1342 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0009 | 0/0 | 1342 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0010 | 0/0 | 1342 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0011 | 0/0 | 1342 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| t0012 | 0/0 | 1342 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0006 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3570 | 161 | 36 | 27 | 69 | 8 | 19 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0002 | 0/0 | 3570 | 34 | 10 | 1 | 19 | 0 | 4 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0004 | 0/0 | 3570 | 12 | 8 | 1 | 2 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0005 | 0/0 | 3570 | 10 | 10 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0006 | 0/0 | 3570 | 5 | 3 | 0 | 0 | 0 | 2 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0008 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0009 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0010 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0015 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0016 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0018 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0019 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0002c0003 | 0/0 | 3570 | 21 | 9 | 3 | 0 | 4 | 5 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0002c0017 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0003c0007 | 0/0 | 3570 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0004c0013 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0005c0012 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0006c0014 | 0/0 | 3570 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0007c0011 | 0/0 | 3570 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4911 | 62 | 16 | 7 | 27 | 1 | 11 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0001t0002 | 1/1 | 4911 | 88 | 17 | 18 | 36 | 7 | 8 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0001t0004 | 0/0 | 4917 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0001t0005 | 0/0 | 4911 | 4 | 0 | 0 | 4 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0001t0007 | 0/0 | 4911 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0001t0009 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0001t0010 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0001t0011 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0002t0001 | 0/0 | 4911 | 25 | 10 | 1 | 10 | 0 | 4 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0002t0002 | 0/0 | 4911 | 5 | 0 | 0 | 5 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0002t0004 | 0/0 | 4917 | 3 | 0 | 0 | 3 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0002t0008 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0004t0001 | 0/0 | 4911 | 12 | 8 | 1 | 2 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0005t0001 | 0/0 | 4911 | 10 | 10 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0006t0001 | 0/0 | 4911 | 4 | 3 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0006t0012 | 0/0 | 4911 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0008t0001 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0009t0002 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0010t0002 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0015t0002 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0016t0002 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0018t0001 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0001c0019t0001 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0002c0003t0003 | 0/0 | 4911 | 21 | 9 | 3 | 0 | 4 | 5 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0002c0017t0003 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0003c0007t0006 | 0/0 | 4899 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0004c0013t0001 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0005c0012t0002 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0006c0014t0001 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| a0007c0011t0001 | 0/0 | 4911 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | copy fasta | chr22 | 49768283 | 49832873 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0006 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0010g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0011g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0006t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0006t0012g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0008t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0009t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0010t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0015t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0016t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0018t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0019t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0017t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0003c0007t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0003c0007t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0004c0013t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0005c0012t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0006c0014t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0007c0011t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00099 | hp2 | a0002 | c0003 | t0003 | g0228 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00140 | hp1 | a0002 | c0003 | t0003 | g0226 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00323 | hp1 | a0002 | c0003 | t0003 | g0224 | EUR | FIN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0152 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01074 | hp1 | a0002 | c0003 | t0003 | g0227 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01074 | hp2 | a0001 | c0015 | t0002 | g0149 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0232 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01109 | hp1 | a0001 | c0018 | t0001 | g0049 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0200 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01261 | hp2 | a0002 | c0003 | t0003 | g0235 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01496 | hp1 | a0001 | c0010 | t0002 | g0131 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0078 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01515 | hp1 | a0002 | c0003 | t0003 | g0221 | EUR | IBS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | IBS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0065 | EUR | IBS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0205 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01884 | hp2 | a0001 | c0019 | t0001 | g0039 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01891 | hp2 | a0002 | c0003 | t0003 | g0236 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0195 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02071 | hp2 | a0001 | c0002 | t0008 | g0012 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CDX | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | CDX | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0198 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02300 | hp1 | a0006 | c0014 | t0001 | g0208 | AMR | PEL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0018 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02572 | hp1 | a0004 | c0013 | t0001 | g0209 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02602 | hp1 | a0002 | c0003 | t0003 | g0223 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02615 | hp1 | a0002 | c0003 | t0003 | g0237 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0193 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02622 | hp1 | a0002 | c0003 | t0003 | g0230 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02717 | hp2 | a0003 | c0007 | t0006 | g0011 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02723 | hp1 | a0002 | c0003 | t0003 | g0234 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0211 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0197 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0196 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0206 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03041 | hp2 | a0001 | c0006 | t0001 | g0057 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0199 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03139 | hp1 | a0001 | c0008 | t0001 | g0019 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0204 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0056 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03239 | hp1 | a0002 | c0003 | t0003 | g0240 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0222 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03516 | hp1 | a0001 | c0006 | t0001 | g0055 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03516 | hp2 | a0002 | c0003 | t0003 | g0238 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0201 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03654 | hp1 | a0007 | c0011 | t0001 | g0181 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0202 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03710 | hp1 | a0001 | c0006 | t0012 | g0241 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03710 | hp2 | a0002 | c0003 | t0003 | g0229 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03942 | hp1 | a0001 | c0006 | t0001 | g0050 | SAS | BEB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0233 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18522 | hp2 | a0003 | c0007 | t0006 | g0004 | AFR | YRI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0016 | EAS | CHB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0192 | AFR | YRI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18969 | hp2 | a0001 | c0016 | t0002 | g0160 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18974 | hp2 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0010 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19055 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19058 | hp2 | a0005 | c0012 | t0002 | g0159 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19088 | hp1 | a0001 | c0001 | t0009 | g0128 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0203 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0207 | AFR | YRI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | YRI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ASW | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | TSI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | GIH | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | GIH | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0210 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0010 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02559 | hp1 | a0001 | c0009 | t0002 | g0066 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02559 | hp2 | a0003 | c0007 | t0006 | g0004 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0191 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03471 | hp2 | a0002 | c0017 | t0003 | g0231 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG06807 | hp1 | a0002 | c0003 | t0003 | g0239 | AFR | USA | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | USA | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | USA | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | USA | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA21309 | hp2 | a0002 | c0003 | t0003 | g0225 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0071 | REF | REF | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0062 | REF | REF | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49777735
|
C | A | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2936G>T | p.Arg979Leu | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 9/13 | 3327/4911 | 2936/3570 | 979/1189 | chr22 | 49777735 | ||
| chr22:49794067
|
C | T | 1 | a0003 | 3 | HG02559.hp2 HG02717.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.2326G>A | p.Gly776Arg | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/13 | 2717/4911 | 2326/3570 | 776/1189 | chr22 | 49794067 | ||
| chr22:49794205
|
C | T | 1 | a0002 | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
missense_variant | MODERATE | c.2188G>A | p.Ala730Thr | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/13 | 2579/4911 | 2188/3570 | 730/1189 | chr22 | 49794205 | ||
| chr22:49798580
|
G | A | 1 | a0005 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1763C>T | p.Ala588Val | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 5/13 | 2154/4911 | 1763/3570 | 588/1189 | chr22 | 49798580 | ||
| chr22:49822993
|
G | A | 1 | a0006 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1325C>T | p.Ala442Val | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 1716/4911 | 1325/3570 | 442/1189 | chr22 | 49822993 | ||
| chr22:49823077
|
T | C | 1 | a0007 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1241A>G | p.Glu414Gly | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 1632/4911 | 1241/3570 | 414/1189 | chr22 | 49823077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49774254
|
G | A | 1 | a0004c0013 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.3549C>T | p.Ser1183Ser | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 3940/4911 | 3549/3570 | 1183/1189 | chr22 | 49774254 | ||
| chr22:49774275
|
G | A | 1 | a0001c0018 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.3528C>T | p.Arg1176Arg | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 3919/4911 | 3528/3570 | 1176/1189 | chr22 | 49774275 | ||
| chr22:49776122
|
G | A | 1 | a0001c0005 | 10 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
synonymous_variant | LOW | c.3159C>T | p.Ala1053Ala | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/13 | 3550/4911 | 3159/3570 | 1053/1189 | chr22 | 49776122 | ||
| chr22:49777035
|
G | A | 1 | a0002c0017 | 1 | HG03471.hp2 | splice_region_variant&synonymous_variant | LOW | c.3120C>T | p.Ala1040Ala | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/13 | 3511/4911 | 3120/3570 | 1040/1189 | chr22 | 49777035 | ||
| chr22:49777095
|
G | A | 1 | a0003c0007 | 3 | HG02559.hp2 HG02717.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.3060C>T | p.Arg1020Arg | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/13 | 3451/4911 | 3060/3570 | 1020/1189 | chr22 | 49777095 | ||
| chr22:49787667
|
G | A | 1 | a0001c0010 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.2580C>T | p.Gly860Gly | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/13 | 2971/4911 | 2580/3570 | 860/1189 | chr22 | 49787667 | ||
| chr22:49799030
|
C | T | 1 | a0001c0009 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1614G>A | p.Leu538Leu | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 4/13 | 2005/4911 | 1614/3570 | 538/1189 | chr22 | 49799030 | ||
| chr22:49823091
|
G | A | 4 | a0001c0004a0001c0005a0004c0013others(1): Show | 24 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(21): Show |
synonymous_variant | LOW | c.1227C>T | p.Gly409Gly | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 1618/4911 | 1227/3570 | 409/1189 | chr22 | 49823091 | ||
| chr22:49823106
|
G | A | 8 | a0001c0002a0001c0004a0001c0005others(5): Show | 61 | HG01256.hp2 HG01361.hp2 HG01884.hp1 others(58): Show |
synonymous_variant | LOW | c.1212C>T | p.Val404Val | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 1603/4911 | 1212/3570 | 404/1189 | chr22 | 49823106 | ||
| chr22:49823115
|
G | A | 1 | a0001c0015 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.1203C>T | p.Tyr401Tyr | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 1594/4911 | 1203/3570 | 401/1189 | chr22 | 49823115 | ||
| chr22:49823316
|
G | A | 1 | a0001c0016 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.1002C>T | p.Gly334Gly | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 1393/4911 | 1002/3570 | 334/1189 | chr22 | 49823316 | ||
| chr22:49823739
|
G | A | 4 | a0001c0006a0001c0018a0002c0003others(1): Show | 28 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(25): Show |
synonymous_variant | LOW | c.579C>T | p.Phe193Phe | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 970/4911 | 579/3570 | 193/1189 | chr22 | 49823739 | ||
| chr22:49823985
|
C | T | 1 | a0001c0008 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.333G>A | p.Pro111Pro | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 724/4911 | 333/3570 | 111/1189 | chr22 | 49823985 | ||
| chr22:49824180
|
C | A | 1 | a0001c0019 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.138G>T | p.Gly46Gly | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/13 | 529/4911 | 138/3570 | 46/1189 | chr22 | 49824180 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49773718
|
C | T | 1 | a0001c0001t0005 | 4 | NA18966.hp1 NA18995.hp1 NA19085.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*515G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 515 | chr22 | 49773718 | |||||
| chr22:49773739
|
C | T | 1 | a0001c0001t0009 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 494 | chr22 | 49773739 | |||||
| chr22:49774000
|
G | A | 1 | a0001c0001t0010 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*233C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 233 | chr22 | 49774000 | |||||
| chr22:49774004
|
T | C | 21 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(18): Show | 158 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*229A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 229 | chr22 | 49774004 | |||||
| chr22:49774005
|
G | A | 1 | a0001c0006t0012 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 228 | chr22 | 49774005 | |||||
| chr22:49774036
|
G | A | 1 | a0001c0001t0007 | 3 | HG02622.hp2 HG02818.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*197C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 197 | chr22 | 49774036 | |||||
| chr22:49774115
|
G | A | 1 | a0001c0001t0011 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 13/13 | 118 | chr22 | 49774115 | |||||
| chr22:49827708
|
G | GCGGGCT | 2 | a0001c0001t0004a0001c0002t0004 | 4 | HG00597.hp2 NA18612.hp1 NA18974.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-232_-227dupAGCCCG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/13 | 3392 | chr22 | 49827708 | |||||
| chr22:49827718
|
G | T | 1 | a0001c0002t0008 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-236C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/13 | 3401 | chr22 | 49827718 | |||||
| chr22:49827759
|
GGCGGGCG others(5): Show |
G | 1 | a0003c0007t0006 | 3 | HG02559.hp2 HG02717.hp2 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-289_-278delGCCCGC others(6): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/13 | 3443 | chr22 | 49827759 | |||||
| chr22:49827828
|
T | C | 3 | a0001c0006t0012a0002c0003t0003a0002c0017t0003 | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-346A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/13 | 3511 | chr22 | 49827828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49774478
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0003c0007t0006g0004others(1): Show | 5 | HG02145.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3387-62T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49774478 | ||||||
| chr22:49774479
|
T | G | 5 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0217others(2): Show | 5 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.3387-63A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49774479 | ||||||
| chr22:49774616
|
C | G | 26 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(23): Show | 27 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.3387-200G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49774616 | ||||||
| chr22:49774617
|
G | A | 14 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 14 | HG00673.hp1 HG01256.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.3387-201C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49774617 | ||||||
| chr22:49774772
|
G | A | 1 | a0002c0003t0003g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3387-356C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49774772 | ||||||
| chr22:49774928
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3387-512C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49774928 | ||||||
| chr22:49774937
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0194 | 3 | HG02886.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3387-521G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49774937 | ||||||
| chr22:49775016
|
G | A | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3386+575C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49775016 | ||||||
| chr22:49775049
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0003c0007t0006g0004others(1): Show | 5 | HG02145.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3386+542G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49775049 | ||||||
| chr22:49775099
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3386+492G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49775099 | ||||||
| chr22:49775105
|
C | T | 1 | a0006c0014t0001g0208 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3386+486G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49775105 | ||||||
| chr22:49775509
|
A | G | 135 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(132): Show | 141 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.3386+82T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49775509 | ||||||
| chr22:49775557
|
G | A | 59 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(56): Show | 62 | HG00597.hp2 HG01256.hp2 HG01361.hp2 others(59): Show |
intron_variant | MODIFIER | c.3386+34C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 12/12 | chr22 | 49775557 | ||||||
| chr22:49775773
|
T | C | 69 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(66): Show | 72 | HG00597.hp2 HG01256.hp2 HG01361.hp2 others(69): Show |
intron_variant | MODIFIER | c.3232-28A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775773 | ||||||
| chr22:49775815
|
A | AC | 19 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp1 HG00558.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.3232-71dupG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775815 | ||||||
| chr22:49775815
|
ACCCC | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG01891.hp1 HG02897.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.3232-74_3232-71del others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775815 | ||||||
| chr22:49775816
|
C | CCCCCCCC others(33): Show |
1 | a0001c0001t0002g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3232-72_3232-71ins others(40): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775816 | ||||||
| chr22:49775817
|
C | CCCCCCCC others(172): Show |
1 | a0001c0001t0011g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3232-73_3232-72ins others(179): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775817 | ||||||
| chr22:49775817
|
C | CCCCCCCC others(171): Show |
1 | a0001c0002t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3232-73_3232-72ins others(178): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775817 | ||||||
| chr22:49775817
|
C | CCCCCCCC others(134): Show |
1 | a0001c0002t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3232-73_3232-72ins others(141): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775817 | ||||||
| chr22:49775819
|
C | CCCACCGC others(170): Show |
1 | a0001c0004t0001g0191 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(177): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCC others(69): Show |
1 | a0001c0001t0004g0013 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(76): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCG others(32): Show |
1 | a0001c0001t0002g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(39): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCG others(135): Show |
1 | a0001c0001t0005g0151 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(142): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCG others(171): Show |
1 | a0001c0001t0001g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(178): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCG others(171): Show |
10 | a0001c0001t0002g0082a0001c0001t0002g0109a0001c0002t0001g0032others(7): Show | 11 | HG01071.hp1 HG01261.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3232-75_3232-74ins others(178): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCG others(68): Show |
7 | a0001c0001t0002g0123a0001c0001t0002g0147a0001c0001t0002g0162others(4): Show | 7 | HG01361.hp2 HG01975.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.3232-75_3232-74ins others(75): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCG others(207): Show |
1 | a0001c0002t0001g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(214): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCCG others(175): Show |
1 | a0002c0017t0003g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(182): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCGC others(170): Show |
1 | a0001c0001t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(177): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCGC others(170): Show |
12 | a0001c0001t0001g0143a0001c0001t0001g0170a0001c0001t0001g0175others(9): Show | 12 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.3232-75_3232-74ins others(177): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCGC others(67): Show |
3 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0019t0001g0039 | 3 | HG01884.hp2 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.3232-75_3232-74ins others(74): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCGC others(103): Show |
1 | a0001c0001t0001g0090 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(110): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCGC others(139): Show |
1 | a0001c0002t0001g0037 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(146): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCCGG others(171): Show |
1 | a0001c0002t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(178): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCGCC others(133): Show |
1 | a0001c0005t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(140): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCCGCC others(169): Show |
16 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0168others(13): Show | 17 | HG00438.hp1 HG00673.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.3232-75_3232-74ins others(176): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCCCGCCG others(171): Show |
1 | a0001c0001t0002g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(178): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCGCCGCC others(170): Show |
1 | a0001c0001t0001g0047 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(177): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCGCCGCC others(169): Show |
1 | a0001c0004t0001g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3232-75_3232-74ins others(176): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775819
|
C | CCGCCGCC others(169): Show |
14 | a0001c0001t0001g0044a0001c0001t0001g0180a0001c0001t0007g0211others(11): Show | 14 | HG01256.hp2 HG02040.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3232-75_3232-74ins others(176): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775819 | ||||||
| chr22:49775821
|
C | G | 8 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0179others(5): Show | 8 | HG01433.hp1 HG02040.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.3232-76G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775821 | ||||||
| chr22:49775822
|
C | A | 1 | a0001c0005t0001g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3232-77G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775822 | ||||||
| chr22:49775823
|
C | CGCCCCCC others(127): Show |
1 | a0001c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3232-79_3232-78ins others(134): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775823 | ||||||
| chr22:49775823
|
C | CGCCCCCC others(127): Show |
8 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0163others(5): Show | 8 | HG00642.hp2 HG01433.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.3232-79_3232-78ins others(134): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775823 | ||||||
| chr22:49775823
|
C | CGCCCCCC others(163): Show |
1 | a0001c0001t0001g0166 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3232-79_3232-78ins others(170): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775823 | ||||||
| chr22:49775823
|
C | CGCCCCCC others(24): Show |
1 | a0001c0002t0001g0216 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3232-79_3232-78ins others(31): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775823 | ||||||
| chr22:49775824
|
C | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG01255.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3232-79G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775824 | ||||||
| chr22:49775825
|
G | A | 4 | a0001c0001t0002g0112a0001c0001t0005g0008a0001c0001t0005g0150others(1): Show | 5 | HG02717.hp2 NA18943.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.3232-80C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775825 | ||||||
| chr22:49775825
|
G | C | 13 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0163others(10): Show | 13 | HG00642.hp2 HG01255.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.3232-80C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775825 | ||||||
| chr22:49775825
|
G | GGCCCCCC others(127): Show |
1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3232-81_3232-80ins others(134): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775825 | ||||||
| chr22:49775825
|
GCCTC | G | 5 | a0001c0001t0002g0069a0001c0008t0001g0019a0002c0003t0003g0010others(2): Show | 6 | HG02486.hp2 HG03139.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3232-84_3232-81del others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775825 | ||||||
| chr22:49775828
|
T | C | 22 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0163others(19): Show | 24 | HG00140.hp1 HG00642.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3232-83A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775828 | ||||||
| chr22:49775828
|
T | G | 19 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 19 | HG01891.hp1 HG01891.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.3232-83A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775828 | ||||||
| chr22:49775829
|
C | G | 4 | a0001c0001t0001g0043a0001c0004t0001g0196a0001c0018t0001g0049others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3232-84G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775829 | ||||||
| chr22:49775831
|
C | CG | 3 | a0001c0001t0001g0188a0001c0005t0001g0193a0007c0011t0001g0181 | 3 | HG02615.hp2 HG03654.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3232-87_3232-86ins others(1): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775831 | ||||||
| chr22:49775831
|
C | CGCAGCTG others(128): Show |
5 | a0001c0001t0001g0165a0001c0001t0001g0173a0002c0003t0003g0225others(2): Show | 5 | HG00140.hp1 HG01074.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.3232-87_3232-86ins others(135): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775831 | ||||||
| chr22:49775831
|
C | G | 14 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0163others(11): Show | 14 | HG00642.hp2 HG01106.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.3232-86G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775831 | ||||||
| chr22:49775832
|
CA | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG01891.hp1 HG01891.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.3232-88delT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775832 | ||||||
| chr22:49775833
|
A | C | 26 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0048others(23): Show | 27 | HG00140.hp1 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.3232-88T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775833 | ||||||
| chr22:49775833
|
A | G | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3232-88T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775833 | ||||||
| chr22:49775834
|
C | G | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02615.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.3232-89G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775834 | ||||||
| chr22:49775835
|
C | CTGTGTGA others(91): Show |
5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01255.hp2 HG02615.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.3232-91_3232-90ins others(98): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775835 | ||||||
| chr22:49775836
|
C | CCG | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3232-92_3232-91ins others(2): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775836 | ||||||
| chr22:49775836
|
C | G | 46 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 47 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.3232-91G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775836 | ||||||
| chr22:49775859
|
C | A | 9 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0179others(6): Show | 11 | HG00323.hp1 HG01515.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3232-114G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775859 | ||||||
| chr22:49775861
|
A | T | 9 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0179others(6): Show | 11 | HG00323.hp1 HG01515.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3232-116T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775861 | ||||||
| chr22:49775869
|
G | GCCCCCCC others(98): Show |
1 | a0001c0001t0002g0141 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3232-125_3232-124i others(107): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775869 | ||||||
| chr22:49775878
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3232-133C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775878 | ||||||
| chr22:49775887
|
C | T | 6 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01106.hp1 HG01255.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3232-142G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775887 | ||||||
| chr22:49775919
|
T | C | 5 | a0001c0001t0001g0194a0001c0001t0002g0069a0001c0001t0002g0130others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.3231+131A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775919 | ||||||
| chr22:49775930
|
G | GC | 9 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0169others(6): Show | 9 | HG00438.hp1 HG00741.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.3231+119dupG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775930 | ||||||
| chr22:49775937
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3231+113G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775937 | ||||||
| chr22:49775950
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3231+100T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775950 | ||||||
| chr22:49775957
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3231+93A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775957 | ||||||
| chr22:49775958
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3231+92C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775958 | ||||||
| chr22:49775963
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3231+87T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775963 | ||||||
| chr22:49775968
|
C | CCCGCAGC others(3): Show |
1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3231+81_3231+82ins others(10): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49775968 | ||||||
| chr22:49776028
|
G | A | 10 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(7): Show | 10 | HG01255.hp2 HG02451.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.3231+22C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49776028 | ||||||
| chr22:49776043
|
T | C | 1 | a0001c0006t0012g0241 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.3231+7A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 11/12 | chr22 | 49776043 | ||||||
| chr22:49776204
|
G | A | 19 | a0001c0001t0001g0163a0001c0001t0001g0167a0001c0001t0001g0170others(16): Show | 19 | HG00438.hp1 HG00642.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.3122-45C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776204 | ||||||
| chr22:49776216
|
G | A | 1 | a0002c0003t0003g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3122-57C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776216 | ||||||
| chr22:49776231
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3122-72C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776231 | ||||||
| chr22:49776277
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3122-118G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776277 | ||||||
| chr22:49776425
|
G | C | 1 | a0001c0001t0002g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3122-266C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776425 | ||||||
| chr22:49776461
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3122-302C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776461 | ||||||
| chr22:49776469
|
G | A | 2 | a0002c0003t0003g0010a0002c0003t0003g0236 | 3 | HG01891.hp2 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3122-310C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776469 | ||||||
| chr22:49776546
|
G | A | 2 | a0001c0001t0001g0163a0007c0011t0001g0181 | 2 | HG00642.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3122-387C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776546 | ||||||
| chr22:49776674
|
G | T | 2 | a0002c0003t0003g0222a0002c0003t0003g0223 | 2 | HG02602.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3121+360C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776674 | ||||||
| chr22:49776833
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3121+201C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776833 | ||||||
| chr22:49776856
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3121+178T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49776856 | ||||||
| chr22:49777026
|
C | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0093others(1): Show | 4 | HG00741.hp1 HG03688.hp2 HG03927.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3121+8G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 10/12 | chr22 | 49777026 | ||||||
| chr22:49777279
|
G | T | 6 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 8 | HG01255.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2994-118C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 9/12 | chr22 | 49777279 | ||||||
| chr22:49777289
|
G | A | 128 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(125): Show | 132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.2994-128C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 9/12 | chr22 | 49777289 | ||||||
| chr22:49777298
|
G | C | 4 | a0001c0001t0002g0045a0001c0001t0002g0077a0001c0001t0010g0078others(1): Show | 4 | HG01496.hp2 HG02723.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2994-137C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 9/12 | chr22 | 49777298 | ||||||
| chr22:49777320
|
G | A | 2 | a0001c0004t0001g0189a0001c0004t0001g0190 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2994-159C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 9/12 | chr22 | 49777320 | ||||||
| chr22:49777519
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2993+159C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 9/12 | chr22 | 49777519 | ||||||
| chr22:49777627
|
C | T | 22 | a0001c0006t0001g0050a0001c0006t0012g0241a0002c0003t0003g0010others(19): Show | 23 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2993+51G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 9/12 | chr22 | 49777627 | ||||||
| chr22:49777826
|
C | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2858-13G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49777826 | ||||||
| chr22:49777879
|
A | T | 7 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(4): Show | 7 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2858-66T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49777879 | ||||||
| chr22:49777880
|
C | T | 7 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(4): Show | 7 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2858-67G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49777880 | ||||||
| chr22:49778145
|
G | T | 1 | a0001c0001t0002g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2858-332C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778145 | ||||||
| chr22:49778150
|
T | A | 8 | a0001c0004t0001g0197a0001c0005t0001g0009a0001c0005t0001g0198others(5): Show | 9 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2858-337A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778150 | ||||||
| chr22:49778179
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2858-366G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778179 | ||||||
| chr22:49778206
|
G | A | 24 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(21): Show | 26 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.2858-393C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778206 | ||||||
| chr22:49778214
|
G | A | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2858-401C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778214 | ||||||
| chr22:49778258
|
T | C | 23 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(20): Show | 24 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2858-445A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778258 | ||||||
| chr22:49778389
|
A | G | 27 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(24): Show | 28 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.2858-576T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778389 | ||||||
| chr22:49778578
|
G | A | 28 | a0001c0001t0001g0143a0001c0006t0001g0050a0001c0006t0001g0055others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2858-765C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778578 | ||||||
| chr22:49778604
|
C | T | 1 | a0001c0005t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2858-791G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778604 | ||||||
| chr22:49778633
|
T | C | 26 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(23): Show | 27 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.2858-820A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778633 | ||||||
| chr22:49778662
|
AT | A | 7 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(4): Show | 7 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2858-850delA | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778662 | ||||||
| chr22:49778684
|
C | G | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2858-871G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778684 | ||||||
| chr22:49778685
|
G | A | 1 | a0004c0013t0001g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2858-872C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778685 | ||||||
| chr22:49778807
|
G | A | 78 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(75): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.2858-994C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778807 | ||||||
| chr22:49778866
|
T | C | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2858-1053A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778866 | ||||||
| chr22:49778896
|
C | G | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2858-1083G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778896 | ||||||
| chr22:49778949
|
T | C | 30 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0164others(27): Show | 31 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2858-1136A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49778949 | ||||||
| chr22:49779005
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2858-1192G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779005 | ||||||
| chr22:49779023
|
A | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2858-1210T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779023 | ||||||
| chr22:49779097
|
G | A | 1 | a0001c0001t0007g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2858-1284C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779097 | ||||||
| chr22:49779176
|
ATCC | A | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2858-1366_2858-136 others(7): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779176 | ||||||
| chr22:49779268
|
C | T | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2858-1455G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779268 | ||||||
| chr22:49779287
|
C | T | 8 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG00438.hp1 HG01123.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2858-1474G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779287 | ||||||
| chr22:49779312
|
G | A | 1 | a0001c0001t0011g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2858-1499C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779312 | ||||||
| chr22:49779395
|
C | G | 1 | a0001c0004t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2858-1582G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779395 | ||||||
| chr22:49779710
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2858-1897C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779710 | ||||||
| chr22:49779925
|
G | A | 1 | a0002c0003t0003g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2858-2112C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779925 | ||||||
| chr22:49779935
|
GAGCCTGG others(15): Show |
G | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2858-2144_2858-212 others(26): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779935 | ||||||
| chr22:49779962
|
C | T | 1 | a0001c0001t0009g0128 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2858-2149G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779962 | ||||||
| chr22:49779995
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2858-2182C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49779995 | ||||||
| chr22:49780110
|
C | A | 1 | a0001c0001t0002g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2858-2297G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780110 | ||||||
| chr22:49780262
|
A | T | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2858-2449T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780262 | ||||||
| chr22:49780381
|
G | A | 8 | a0001c0001t0002g0153a0001c0002t0002g0154a0001c0002t0002g0155others(5): Show | 8 | HG02155.hp2 NA18612.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.2858-2568C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780381 | ||||||
| chr22:49780397
|
T | C | 8 | a0001c0004t0001g0197a0001c0005t0001g0009a0001c0005t0001g0198others(5): Show | 9 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2858-2584A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780397 | ||||||
| chr22:49780447
|
C | T | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2858-2634G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780447 | ||||||
| chr22:49780475
|
G | A | 4 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0217others(1): Show | 4 | HG02040.hp1 NA18940.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2858-2662C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780475 | ||||||
| chr22:49780580
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2858-2767C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780580 | ||||||
| chr22:49780642
|
C | A | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2858-2829G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780642 | ||||||
| chr22:49780786
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2858-2973G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780786 | ||||||
| chr22:49780787
|
G | A | 1 | a0001c0018t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2858-2974C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780787 | ||||||
| chr22:49780976
|
G | A | 1 | a0001c0006t0001g0057 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2858-3163C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49780976 | ||||||
| chr22:49781002
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2858-3189C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781002 | ||||||
| chr22:49781017
|
C | T | 53 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.2858-3204G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781017 | ||||||
| chr22:49781196
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2858-3383C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781196 | ||||||
| chr22:49781240
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(5): Show | 8 | HG01891.hp1 HG02897.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2858-3427C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781240 | ||||||
| chr22:49781322
|
A | C | 2 | a0001c0001t0002g0113a0001c0001t0002g0116 | 2 | HG00438.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2858-3509T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781322 | ||||||
| chr22:49781440
|
C | T | 3 | a0001c0001t0002g0045a0001c0001t0002g0077a0001c0001t0010g0078 | 3 | HG01496.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2858-3627G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781440 | ||||||
| chr22:49781441
|
G | A | 24 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(21): Show | 25 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.2858-3628C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781441 | ||||||
| chr22:49781497
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0194 | 3 | HG01255.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2858-3684G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781497 | ||||||
| chr22:49781725
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2858-3912G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781725 | ||||||
| chr22:49781831
|
A | C | 2 | a0001c0004t0001g0195a0001c0004t0001g0203 | 2 | HG02040.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2858-4018T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781831 | ||||||
| chr22:49781883
|
C | T | 3 | a0001c0002t0002g0155a0001c0002t0002g0156a0001c0016t0002g0160 | 3 | NA18946.hp1 NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2858-4070G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781883 | ||||||
| chr22:49781948
|
G | A | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2858-4135C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781948 | ||||||
| chr22:49781960
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2858-4147G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781960 | ||||||
| chr22:49781971
|
CGAGACAG others(65): Show |
C | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2858-4230_2858-415 others(76): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781971 | ||||||
| chr22:49781976
|
C | CA | 9 | a0001c0002t0001g0003a0001c0002t0001g0214a0001c0002t0001g0215others(6): Show | 11 | HG02040.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2858-4164dupT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781976 | ||||||
| chr22:49781990
|
A | G | 2 | a0001c0002t0002g0158a0005c0012t0002g0159 | 2 | NA18957.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2858-4177T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49781990 | ||||||
| chr22:49782061
|
TATGTTGC others(143): Show |
T | 1 | a0001c0001t0002g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2858-4398_2858-424 others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782061 | ||||||
| chr22:49782225
|
C | CCGCTCCG others(339): Show |
1 | a0001c0018t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2858-4413_2858-441 others(350): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782225 | ||||||
| chr22:49782282
|
C | T | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2858-4469G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782282 | ||||||
| chr22:49782321
|
G | A | 1 | a0001c0005t0001g0210 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2858-4508C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782321 | ||||||
| chr22:49782338
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2858-4525A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782338 | ||||||
| chr22:49782346
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(10): Show | 14 | HG00741.hp2 HG01433.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2858-4533T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782346 | ||||||
| chr22:49782382
|
G | T | 11 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(8): Show | 11 | HG01256.hp2 HG01433.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.2858-4569C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782382 | ||||||
| chr22:49782412
|
G | A | 3 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056 | 3 | HG03209.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2858-4599C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782412 | ||||||
| chr22:49782457
|
C | T | 76 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(73): Show | 80 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2858-4644G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782457 | ||||||
| chr22:49782491
|
GGCCCATC others(472): Show |
G | 1 | a0002c0003t0003g0221 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2857+4420_2858-467 others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782491 | ||||||
| chr22:49782553
|
G | C | 1 | a0001c0001t0002g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2858-4740C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782553 | ||||||
| chr22:49782610
|
A | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2857+4780T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782610 | ||||||
| chr22:49782660
|
ACTCCGCG others(189): Show |
A | 1 | a0001c0001t0001g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2857+4534_2857+472 others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782660 | ||||||
| chr22:49782664
|
C | T | 52 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(49): Show | 55 | HG01256.hp2 HG01361.hp2 HG01433.hp1 others(52): Show |
intron_variant | MODIFIER | c.2857+4726G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782664 | ||||||
| chr22:49782669
|
C | T | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2857+4721G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49782669 | ||||||
| chr22:49783027
|
C | T | 2 | a0002c0003t0003g0234a0002c0003t0003g0235 | 2 | HG01261.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2857+4363G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783027 | ||||||
| chr22:49783115
|
C | T | 3 | a0001c0005t0001g0009a0001c0005t0001g0204a0001c0005t0001g0206 | 4 | HG02922.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2857+4275G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783115 | ||||||
| chr22:49783116
|
G | A | 1 | a0001c0004t0001g0200 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2857+4274C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783116 | ||||||
| chr22:49783214
|
G | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG01255.hp2 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2857+4176C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783214 | ||||||
| chr22:49783234
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2857+4156C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783234 | ||||||
| chr22:49783241
|
A | T | 12 | a0002c0003t0003g0221a0002c0003t0003g0222a0002c0003t0003g0223others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.2857+4149T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783241 | ||||||
| chr22:49783250
|
T | G | 1 | a0001c0001t0002g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2857+4140A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783250 | ||||||
| chr22:49783300
|
A | G | 27 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(24): Show | 28 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.2857+4090T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783300 | ||||||
| chr22:49783317
|
T | C | 17 | a0001c0001t0001g0090a0001c0002t0001g0030a0001c0002t0001g0031others(14): Show | 17 | HG01361.hp2 HG01884.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2857+4073A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783317 | ||||||
| chr22:49783345
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0134 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2857+4045C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783345 | ||||||
| chr22:49783380
|
C | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2857+4010G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783380 | ||||||
| chr22:49783450
|
G | A | 1 | a0001c0001t0002g0001 | 6 | HG02109.hp1 HG03195.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2857+3940C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783450 | ||||||
| chr22:49783452
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2857+3938C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783452 | ||||||
| chr22:49783606
|
C | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2857+3784G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783606 | ||||||
| chr22:49783631
|
G | A | 31 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0164others(28): Show | 32 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.2857+3759C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783631 | ||||||
| chr22:49783741
|
G | T | 1 | a0001c0001t0004g0013 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2857+3649C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49783741 | ||||||
| chr22:49784051
|
C | A | 1 | a0001c0001t0011g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2857+3339G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784051 | ||||||
| chr22:49784110
|
G | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2857+3280C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784110 | ||||||
| chr22:49784222
|
G | GGACAAAG others(75): Show |
1 | a0001c0004t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2857+3086_2857+316 others(86): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784222 | ||||||
| chr22:49784322
|
G | A | 23 | a0001c0008t0001g0019a0001c0019t0001g0039a0002c0003t0003g0010others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.2857+3068C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784322 | ||||||
| chr22:49784372
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2857+3018G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784372 | ||||||
| chr22:49784381
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2857+3009C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784381 | ||||||
| chr22:49784416
|
G | C | 1 | a0001c0018t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2857+2974C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784416 | ||||||
| chr22:49784434
|
A | G | 104 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(101): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2857+2956T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784434 | ||||||
| chr22:49784491
|
C | A | 3 | a0001c0001t0002g0091a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG02572.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2857+2899G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784491 | ||||||
| chr22:49784640
|
G | A | 41 | a0001c0001t0001g0090a0001c0002t0001g0003a0001c0002t0001g0030others(38): Show | 44 | HG01256.hp2 HG01361.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.2857+2750C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784640 | ||||||
| chr22:49784759
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2857+2631G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784759 | ||||||
| chr22:49784794
|
G | A | 26 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0006t0001g0050others(23): Show | 27 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.2857+2596C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784794 | ||||||
| chr22:49784810
|
G | A | 21 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(18): Show | 22 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.2857+2580C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784810 | ||||||
| chr22:49784921
|
C | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2857+2469G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784921 | ||||||
| chr22:49784946
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2857+2444G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49784946 | ||||||
| chr22:49785024
|
T | C | 21 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(18): Show | 22 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.2857+2366A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785024 | ||||||
| chr22:49785101
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2857+2289G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785101 | ||||||
| chr22:49785164
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2857+2226C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785164 | ||||||
| chr22:49785200
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2857+2190C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785200 | ||||||
| chr22:49785238
|
G | A | 1 | a0001c0004t0001g0200 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2857+2152C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785238 | ||||||
| chr22:49785269
|
A | G | 133 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(130): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.2857+2121T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785269 | ||||||
| chr22:49785276
|
C | T | 2 | a0001c0006t0001g0050a0001c0006t0012g0241 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2857+2114G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785276 | ||||||
| chr22:49785309
|
G | A | 1 | a0002c0003t0003g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2857+2081C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785309 | ||||||
| chr22:49785347
|
G | A | 7 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(4): Show | 7 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2857+2043C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785347 | ||||||
| chr22:49785410
|
G | A | 3 | a0001c0001t0002g0045a0001c0001t0002g0077a0001c0001t0010g0078 | 3 | HG01496.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2857+1980C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785410 | ||||||
| chr22:49785464
|
C | T | 1 | a0001c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2857+1926G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785464 | ||||||
| chr22:49785689
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2857+1701T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785689 | ||||||
| chr22:49785849
|
A | C | 1 | a0001c0002t0001g0217 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2857+1541T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785849 | ||||||
| chr22:49785858
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2857+1532G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785858 | ||||||
| chr22:49785885
|
C | T | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2857+1505G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785885 | ||||||
| chr22:49785939
|
A | G | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2857+1451T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785939 | ||||||
| chr22:49785992
|
C | T | 40 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 43 | HG00741.hp2 HG01255.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.2857+1398G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49785992 | ||||||
| chr22:49786002
|
C | G | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2857+1388G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786002 | ||||||
| chr22:49786003
|
G | A | 30 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 31 | HG00741.hp2 HG01255.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.2857+1387C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786003 | ||||||
| chr22:49786011
|
G | A | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2857+1379C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786011 | ||||||
| chr22:49786072
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2857+1318G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786072 | ||||||
| chr22:49786073
|
C | G | 1 | a0001c0001t0002g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2857+1317G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786073 | ||||||
| chr22:49786090
|
C | G | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0011g0152others(26): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.2857+1300G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786090 | ||||||
| chr22:49786253
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2857+1137C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786253 | ||||||
| chr22:49786366
|
AGCAGAGG others(2): Show |
A | 9 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0002t0001g0214others(6): Show | 9 | HG02040.hp1 HG02056.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2857+1015_2857+102 others(13): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786366 | ||||||
| chr22:49786388
|
C | A | 1 | a0001c0001t0002g0115 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2857+1002G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786388 | ||||||
| chr22:49786407
|
C | T | 35 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(32): Show | 37 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.2857+983G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786407 | ||||||
| chr22:49786534
|
T | C | 2 | a0002c0003t0003g0234a0002c0003t0003g0235 | 2 | HG01261.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2857+856A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786534 | ||||||
| chr22:49786557
|
A | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2857+833T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786557 | ||||||
| chr22:49786686
|
T | C | 1 | a0001c0005t0001g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2857+704A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786686 | ||||||
| chr22:49786810
|
T | G | 1 | a0001c0002t0001g0216 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2857+580A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786810 | ||||||
| chr22:49786849
|
A | C | 62 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(59): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2857+541T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786849 | ||||||
| chr22:49786913
|
C | A | 21 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(18): Show | 22 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.2857+477G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786913 | ||||||
| chr22:49786917
|
AC | A | 82 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2857+472delG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786917 | ||||||
| chr22:49786922
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2857+468G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786922 | ||||||
| chr22:49786968
|
C | G | 21 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(18): Show | 21 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.2857+422G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49786968 | ||||||
| chr22:49787002
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2857+388C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787002 | ||||||
| chr22:49787066
|
A | G | 133 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(130): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.2857+324T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787066 | ||||||
| chr22:49787282
|
A | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2857+108T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787282 | ||||||
| chr22:49787297
|
A | ACCCCCCC others(6): Show |
1 | a0001c0001t0001g0023 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2857+92_2857+93ins others(13): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787297 | ||||||
| chr22:49787299
|
A | AC | 37 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0089others(34): Show | 38 | HG00140.hp2 HG00323.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.2857+90dupG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787299 | ||||||
| chr22:49787299
|
A | ACCCCCCC others(4): Show |
2 | a0001c0001t0001g0026a0001c0001t0001g0042 | 2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2857+80_2857+90dup others(11): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787299 | ||||||
| chr22:49787299
|
A | ACCCCCCC others(5): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0025 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2857+79_2857+90dup others(12): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787299 | ||||||
| chr22:49787299
|
A | ACCCCCCC others(6): Show |
1 | a0001c0001t0001g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2857+78_2857+90dup others(13): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787299 | ||||||
| chr22:49787299
|
A | ACCCCCCC others(7): Show |
1 | a0001c0001t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2857+90_2857+91ins others(14): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787299 | ||||||
| chr22:49787299
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2857+91T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787299 | ||||||
| chr22:49787299
|
AC | A | 40 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0163others(37): Show | 48 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.2857+90delG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787299 | ||||||
| chr22:49787302
|
C | CG | 27 | a0001c0001t0001g0048a0001c0001t0001g0090a0001c0001t0001g0178others(24): Show | 27 | HG00597.hp2 HG01361.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.2857+87_2857+88ins others(1): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787302 | ||||||
| chr22:49787303
|
C | G | 50 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0053others(47): Show | 53 | HG00438.hp1 HG01123.hp1 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.2857+87G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787303 | ||||||
| chr22:49787304
|
C | G | 34 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0163others(31): Show | 37 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.2857+86G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787304 | ||||||
| chr22:49787306
|
C | T | 2 | a0001c0001t0001g0090a0001c0002t0001g0037 | 2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2857+84G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787306 | ||||||
| chr22:49787307
|
C | CG | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2857+82_2857+83ins others(1): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787307 | ||||||
| chr22:49787310
|
C | G | 1 | a0001c0001t0002g0071 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2857+80G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787310 | ||||||
| chr22:49787357
|
AG | A | 5 | a0001c0001t0002g0076a0001c0001t0002g0091a0001c0001t0002g0101others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2857+32delC | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787357 | ||||||
| chr22:49787381
|
G | A | 1 | a0001c0001t0005g0151 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2857+9C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 8/12 | chr22 | 49787381 | ||||||
| chr22:49787922
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2360-35G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49787922 | ||||||
| chr22:49788084
|
C | A | 1 | a0001c0001t0002g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2360-197G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788084 | ||||||
| chr22:49788169
|
G | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG01255.hp2 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2360-282C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788169 | ||||||
| chr22:49788184
|
GAC | G | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2360-299_2360-298d others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788184 | ||||||
| chr22:49788267
|
C | T | 24 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(21): Show | 25 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.2360-380G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788267 | ||||||
| chr22:49788312
|
C | A | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.2360-425G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788312 | ||||||
| chr22:49788392
|
G | C | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2360-505C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788392 | ||||||
| chr22:49788509
|
C | G | 1 | a0001c0001t0002g0087 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2360-622G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788509 | ||||||
| chr22:49788511
|
G | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG01891.hp1 HG02897.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2360-624C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788511 | ||||||
| chr22:49788537
|
A | G | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2360-650T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788537 | ||||||
| chr22:49788679
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2360-792C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49788679 | ||||||
| chr22:49789021
|
A | C | 8 | a0001c0004t0001g0197a0001c0005t0001g0009a0001c0005t0001g0198others(5): Show | 9 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2360-1134T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789021 | ||||||
| chr22:49789054
|
T | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(6): Show | 10 | HG00741.hp2 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2360-1167A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789054 | ||||||
| chr22:49789191
|
G | A | 21 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(18): Show | 22 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.2360-1304C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789191 | ||||||
| chr22:49789218
|
C | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2360-1331G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789218 | ||||||
| chr22:49789298
|
G | C | 4 | a0002c0003t0003g0225a0002c0003t0003g0226a0002c0003t0003g0227others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-1411C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789298 | ||||||
| chr22:49789490
|
T | TC | 14 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0164others(11): Show | 15 | HG00642.hp2 HG00673.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.2360-1604dupG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789490 | ||||||
| chr22:49789495
|
C | A | 1 | a0001c0001t0002g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2360-1608G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789495 | ||||||
| chr22:49789495
|
C | T | 1 | a0001c0018t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2360-1608G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789495 | ||||||
| chr22:49789497
|
C | G | 26 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(23): Show | 27 | HG00597.hp2 HG00741.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.2360-1610G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789497 | ||||||
| chr22:49789499
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2360-1612G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789499 | ||||||
| chr22:49789499
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 12 | HG01361.hp2 HG01891.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2360-1612G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789499 | ||||||
| chr22:49789500
|
G | C | 1 | a0001c0001t0002g0136 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2360-1613C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789500 | ||||||
| chr22:49789513
|
G | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2360-1626C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789513 | ||||||
| chr22:49789514
|
C | T | 122 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(119): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.2360-1627G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789514 | ||||||
| chr22:49789522
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0174 | 2 | HG01123.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2360-1635T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789522 | ||||||
| chr22:49789601
|
T | C | 20 | a0001c0002t0001g0003a0001c0004t0001g0196a0002c0003t0003g0010others(17): Show | 23 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2360-1714A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789601 | ||||||
| chr22:49789718
|
C | T | 1 | a0002c0003t0003g0237 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2360-1831G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789718 | ||||||
| chr22:49789778
|
C | G | 1 | a0001c0002t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2360-1891G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789778 | ||||||
| chr22:49789957
|
G | A | 21 | a0002c0003t0003g0010a0002c0003t0003g0221a0002c0003t0003g0222others(18): Show | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.2360-2070C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789957 | ||||||
| chr22:49789973
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2360-2086G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49789973 | ||||||
| chr22:49790048
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2360-2161T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790048 | ||||||
| chr22:49790067
|
G | T | 3 | a0001c0001t0002g0091a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG02572.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2360-2180C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790067 | ||||||
| chr22:49790184
|
C | T | 2 | a0001c0004t0001g0189a0001c0004t0001g0190 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2360-2297G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790184 | ||||||
| chr22:49790304
|
G | A | 1 | a0001c0001t0010g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2360-2417C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790304 | ||||||
| chr22:49790451
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2360-2564G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790451 | ||||||
| chr22:49790547
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-2660G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790547 | ||||||
| chr22:49790615
|
T | C | 31 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(28): Show | 32 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.2360-2728A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790615 | ||||||
| chr22:49790643
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2360-2756C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790643 | ||||||
| chr22:49790836
|
T | G | 122 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(119): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.2360-2949A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790836 | ||||||
| chr22:49790862
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.2360-2975C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790862 | ||||||
| chr22:49790943
|
G | A | 21 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(18): Show | 22 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.2360-3056C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49790943 | ||||||
| chr22:49791008
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2359+3026C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791008 | ||||||
| chr22:49791171
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2359+2863C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791171 | ||||||
| chr22:49791178
|
C | T | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2359+2856G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791178 | ||||||
| chr22:49791255
|
C | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2359+2779G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791255 | ||||||
| chr22:49791346
|
T | C | 1 | a0001c0004t0001g0200 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2359+2688A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791346 | ||||||
| chr22:49791366
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2359+2668C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791366 | ||||||
| chr22:49791544
|
C | T | 88 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(85): Show | 92 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.2359+2490G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791544 | ||||||
| chr22:49791586
|
C | G | 2 | a0002c0003t0003g0222a0002c0003t0003g0223 | 2 | HG02602.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2359+2448G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791586 | ||||||
| chr22:49791626
|
A | T | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+2408T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791626 | ||||||
| chr22:49791686
|
C | G | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2359+2348G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791686 | ||||||
| chr22:49791695
|
C | T | 76 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0163others(73): Show | 79 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.2359+2339G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791695 | ||||||
| chr22:49791728
|
G | A | 3 | a0001c0001t0002g0065a0001c0001t0002g0072a0001c0009t0002g0066 | 3 | HG01069.hp1 HG01516.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2359+2306C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791728 | ||||||
| chr22:49791737
|
C | T | 21 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(18): Show | 22 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.2359+2297G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791737 | ||||||
| chr22:49791779
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2359+2255C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791779 | ||||||
| chr22:49791784
|
A | G | 119 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(116): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2359+2250T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791784 | ||||||
| chr22:49791866
|
G | A | 18 | a0001c0001t0001g0090a0001c0001t0004g0013a0001c0002t0001g0030others(15): Show | 18 | HG00597.hp2 HG01361.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2359+2168C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49791866 | ||||||
| chr22:49792001
|
T | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2359+2033A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792001 | ||||||
| chr22:49792019
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 8 | HG00741.hp2 HG01433.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2359+2015C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792019 | ||||||
| chr22:49792177
|
TA | T | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.2359+1856delT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792177 | ||||||
| chr22:49792239
|
G | A | 1 | a0001c0018t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2359+1795C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792239 | ||||||
| chr22:49792393
|
G | A | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2359+1641C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792393 | ||||||
| chr22:49792408
|
G | A | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2359+1626C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792408 | ||||||
| chr22:49792571
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2359+1463C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792571 | ||||||
| chr22:49792584
|
G | A | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+1450C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792584 | ||||||
| chr22:49792866
|
G | A | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(6): Show | 10 | HG00741.hp2 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2359+1168C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49792866 | ||||||
| chr22:49793104
|
G | C | 2 | a0001c0002t0001g0051a0001c0002t0001g0052 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2359+930C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793104 | ||||||
| chr22:49793215
|
G | A | 1 | a0001c0002t0008g0012 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2359+819C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793215 | ||||||
| chr22:49793278
|
G | A | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2359+756C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793278 | ||||||
| chr22:49793641
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0111 | 7 | HG02109.hp1 HG03130.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2359+393G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793641 | ||||||
| chr22:49793726
|
A | T | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2359+308T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793726 | ||||||
| chr22:49793731
|
A | G | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2359+303T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793731 | ||||||
| chr22:49793906
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2359+128C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793906 | ||||||
| chr22:49793984
|
A | T | 1 | a0001c0001t0002g0136 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2359+50T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793984 | ||||||
| chr22:49793996
|
G | A | 6 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.2359+38C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793996 | ||||||
| chr22:49793998
|
C | T | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+36G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 7/12 | chr22 | 49793998 | ||||||
| chr22:49794464
|
G | A | 1 | a0001c0010t0002g0131 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2099-170C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49794464 | ||||||
| chr22:49794489
|
C | T | 1 | a0004c0013t0001g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2099-195G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49794489 | ||||||
| chr22:49794657
|
C | T | 1 | a0001c0001t0007g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2099-363G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49794657 | ||||||
| chr22:49794665
|
C | T | 3 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056 | 3 | HG03209.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2099-371G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49794665 | ||||||
| chr22:49794805
|
C | T | 1 | a0001c0004t0001g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2099-511G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49794805 | ||||||
| chr22:49795121
|
A | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2099-827T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795121 | ||||||
| chr22:49795194
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2099-900A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795194 | ||||||
| chr22:49795269
|
G | A | 1 | a0001c0006t0001g0057 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2099-975C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795269 | ||||||
| chr22:49795317
|
G | A | 1 | a0001c0001t0011g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2099-1023C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795317 | ||||||
| chr22:49795383
|
C | A | 2 | a0001c0006t0001g0050a0001c0006t0012g0241 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2099-1089G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795383 | ||||||
| chr22:49795391
|
GAGAA | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2099-1101_2099-109 others(8): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795391 | ||||||
| chr22:49795564
|
G | T | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2099-1270C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795564 | ||||||
| chr22:49795799
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2099-1505A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49795799 | ||||||
| chr22:49796033
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2099-1739G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796033 | ||||||
| chr22:49796096
|
CT | C | 127 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(124): Show | 132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.2098+1708delA | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796096 | ||||||
| chr22:49796130
|
G | A | 1 | a0001c0019t0001g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2098+1675C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796130 | ||||||
| chr22:49796165
|
A | C | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG01255.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2098+1640T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796165 | ||||||
| chr22:49796355
|
CTTTT | C | 31 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(28): Show | 32 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.2098+1446_2098+144 others(8): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796355 | ||||||
| chr22:49796506
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2098+1299C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796506 | ||||||
| chr22:49796532
|
G | A | 133 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(130): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.2098+1273C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796532 | ||||||
| chr22:49796572
|
G | A | 6 | a0002c0003t0003g0010a0002c0003t0003g0236a0002c0003t0003g0237others(3): Show | 7 | HG01891.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2098+1233C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796572 | ||||||
| chr22:49796575
|
C | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2098+1230G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796575 | ||||||
| chr22:49796585
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2098+1220G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796585 | ||||||
| chr22:49796778
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(6): Show | 10 | HG00741.hp2 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2098+1027T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796778 | ||||||
| chr22:49796822
|
CGGACCCC others(16): Show |
C | 11 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.2098+960_2098+982d others(25): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796822 | ||||||
| chr22:49796823
|
G | A | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2098+982C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796823 | ||||||
| chr22:49796857
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2098+948A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796857 | ||||||
| chr22:49796905
|
A | C | 1 | a0001c0002t0001g0037 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2098+900T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796905 | ||||||
| chr22:49796919
|
G | A | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2098+886C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49796919 | ||||||
| chr22:49797048
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2098+757G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797048 | ||||||
| chr22:49797051
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2098+754A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797051 | ||||||
| chr22:49797129
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2098+676G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797129 | ||||||
| chr22:49797144
|
G | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2098+661C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797144 | ||||||
| chr22:49797282
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2098+523C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797282 | ||||||
| chr22:49797284
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2098+521C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797284 | ||||||
| chr22:49797342
|
C | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 8 | HG00741.hp2 HG01433.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2098+463G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797342 | ||||||
| chr22:49797348
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2098+457C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797348 | ||||||
| chr22:49797448
|
C | G | 2 | a0001c0004t0001g0197a0001c0005t0001g0198 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2098+357G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797448 | ||||||
| chr22:49797488
|
G | C | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2098+317C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797488 | ||||||
| chr22:49797522
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2098+283C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797522 | ||||||
| chr22:49797636
|
T | C | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01255.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2098+169A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797636 | ||||||
| chr22:49797790
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2098+15C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 6/12 | chr22 | 49797790 | ||||||
| chr22:49798242
|
G | T | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1786-125C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 5/12 | chr22 | 49798242 | ||||||
| chr22:49798280
|
C | T | 5 | a0001c0005t0001g0009a0001c0005t0001g0204a0001c0005t0001g0205others(2): Show | 6 | HG01884.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786-163G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 5/12 | chr22 | 49798280 | ||||||
| chr22:49798324
|
G | A | 91 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(88): Show | 96 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1786-207C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 5/12 | chr22 | 49798324 | ||||||
| chr22:49798523
|
A | G | 1 | a0002c0003t0003g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1785+35T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 5/12 | chr22 | 49798523 | ||||||
| chr22:49798526
|
C | T | 47 | a0001c0001t0001g0090a0001c0001t0004g0013a0001c0002t0001g0003others(44): Show | 50 | HG00597.hp2 HG01256.hp2 HG01361.hp2 others(47): Show |
intron_variant | MODIFIER | c.1785+32G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 5/12 | chr22 | 49798526 | ||||||
| chr22:49798749
|
C | G | 2 | a0001c0002t0001g0003a0004c0013t0001g0209 | 4 | HG02257.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1657-63G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 4/12 | chr22 | 49798749 | ||||||
| chr22:49799271
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-152C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799271 | ||||||
| chr22:49799292
|
AGAGGGGA others(20): Show |
A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG01255.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1525-200_1525-174d others(29): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799292 | ||||||
| chr22:49799297
|
G | C | 1 | a0001c0001t0002g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1525-178C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799297 | ||||||
| chr22:49799409
|
G | A | 1 | a0001c0005t0001g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1525-290C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799409 | ||||||
| chr22:49799502
|
A | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525-383T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799502 | ||||||
| chr22:49799524
|
G | A | 18 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(15): Show | 18 | HG00438.hp1 HG01123.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.1525-405C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799524 | ||||||
| chr22:49799576
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1525-457C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799576 | ||||||
| chr22:49799613
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1525-494C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799613 | ||||||
| chr22:49799689
|
T | C | 150 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(147): Show | 158 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1525-570A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799689 | ||||||
| chr22:49799954
|
A | G | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1525-835T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799954 | ||||||
| chr22:49799988
|
T | C | 25 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(22): Show | 25 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1525-869A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49799988 | ||||||
| chr22:49800017
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-898G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800017 | ||||||
| chr22:49800041
|
G | A | 2 | a0001c0005t0001g0192a0001c0005t0001g0193 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1525-922C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800041 | ||||||
| chr22:49800110
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1525-991C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800110 | ||||||
| chr22:49800261
|
C | T | 23 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1525-1142G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800261 | ||||||
| chr22:49800274
|
G | A | 1 | a0001c0001t0002g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1525-1155C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800274 | ||||||
| chr22:49800330
|
G | A | 2 | a0001c0004t0001g0018a0001c0004t0001g0199 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1525-1211C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800330 | ||||||
| chr22:49800511
|
G | T | 22 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(19): Show | 23 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.1525-1392C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800511 | ||||||
| chr22:49800642
|
G | A | 1 | a0001c0004t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1525-1523C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800642 | ||||||
| chr22:49800700
|
A | G | 3 | a0001c0001t0002g0065a0001c0001t0002g0072a0001c0009t0002g0066 | 3 | HG01069.hp1 HG01516.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1525-1581T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800700 | ||||||
| chr22:49800703
|
C | G | 1 | a0001c0004t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1525-1584G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800703 | ||||||
| chr22:49800794
|
C | T | 1 | a0001c0004t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1525-1675G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800794 | ||||||
| chr22:49800821
|
T | A | 1 | a0001c0002t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1525-1702A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800821 | ||||||
| chr22:49800937
|
G | GC | 240 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(237): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1525-1819_1525-181 others(5): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800937 | ||||||
| chr22:49801072
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1525-1953G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801072 | ||||||
| chr22:49801088
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1525-1969G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801088 | ||||||
| chr22:49801350
|
G | A | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110 | 3 | HG00738.hp2 HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1525-2231C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801350 | ||||||
| chr22:49801373
|
AC | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 8 | HG00741.hp2 HG01433.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-2255delG | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801373 | ||||||
| chr22:49801378
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1525-2259C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801378 | ||||||
| chr22:49801544
|
T | C | 42 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 43 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.1525-2425A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801544 | ||||||
| chr22:49801586
|
G | A | 2 | a0001c0002t0001g0051a0001c0002t0001g0052 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1525-2467C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801586 | ||||||
| chr22:49801646
|
A | C | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 29 | HG01255.hp2 HG01891.hp1 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.1525-2527T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801646 | ||||||
| chr22:49801683
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1524+2521C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801683 | ||||||
| chr22:49801727
|
A | G | 23 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(20): Show | 23 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1524+2477T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801727 | ||||||
| chr22:49801759
|
G | A | 11 | a0001c0001t0004g0013a0001c0002t0001g0030a0001c0002t0001g0033others(8): Show | 11 | HG00597.hp2 HG02071.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+2445C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801759 | ||||||
| chr22:49801777
|
G | A | 19 | a0001c0001t0002g0111a0001c0001t0004g0013a0001c0002t0001g0030others(16): Show | 19 | HG00597.hp2 HG01361.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1524+2427C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801777 | ||||||
| chr22:49801868
|
C | T | 7 | a0001c0001t0001g0143a0001c0002t0001g0051a0001c0002t0001g0052others(4): Show | 7 | HG02451.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+2336G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801868 | ||||||
| chr22:49801972
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1524+2232C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49801972 | ||||||
| chr22:49802048
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1524+2156A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802048 | ||||||
| chr22:49802076
|
A | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 8 | HG00741.hp2 HG01433.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1524+2128T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802076 | ||||||
| chr22:49802116
|
A | ATTCCCCA others(87): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1524+2087_1524+208 others(98): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802116 | ||||||
| chr22:49802131
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1524+2073T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802131 | ||||||
| chr22:49802137
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1524+2067C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802137 | ||||||
| chr22:49802137
|
G | GGAGACCA others(40): Show |
1 | a0001c0002t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1524+2020_1524+206 others(51): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802137 | ||||||
| chr22:49802137
|
G | GGAGACCA others(181): Show |
5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0047others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+1879_1524+206 others(192): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802137 | ||||||
| chr22:49802137
|
G | GGAGACCA others(228): Show |
6 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+2066_1524+206 others(239): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802137 | ||||||
| chr22:49802137
|
GGAGACCA others(369): Show |
G | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1524+1691_1524+206 others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802137 | ||||||
| chr22:49802184
|
C | CGAGACCA others(181): Show |
1 | a0002c0003t0003g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1524+2019_1524+202 others(192): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802184 | ||||||
| chr22:49802210
|
T | A | 23 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1524+1994A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802210 | ||||||
| chr22:49802257
|
T | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+1947A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802257 | ||||||
| chr22:49802304
|
A | ATTCCCCA others(40): Show |
2 | a0003c0007t0006g0004a0003c0007t0006g0011 | 3 | HG02559.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1524+1853_1524+189 others(51): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802304 | ||||||
| chr22:49802304
|
A | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+1900T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802304 | ||||||
| chr22:49802318
|
C | TGGGGGCC others(181): Show |
1 | a0001c0002t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1524+1886_1524+188 others(192): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802318 | ||||||
| chr22:49802319
|
GGGGGCCG others(181): Show |
G | 21 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(18): Show | 22 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1524+1697_1524+188 others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802319 | ||||||
| chr22:49802362
|
T | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+1842A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802362 | ||||||
| chr22:49802366
|
G | A | 22 | a0001c0006t0001g0050a0001c0006t0012g0241a0002c0003t0003g0010others(19): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1524+1838C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802366 | ||||||
| chr22:49802366
|
GGGGGCCG others(134): Show |
G | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+1697_1524+183 others(4): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802366 | ||||||
| chr22:49802372
|
C | G | 21 | a0001c0006t0001g0050a0001c0006t0012g0241a0002c0003t0003g0010others(18): Show | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+1832G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802372 | ||||||
| chr22:49802372
|
C | GGAGACCA others(185): Show |
1 | a0002c0003t0003g0221 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1524+1832_1524+183 others(196): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802372 | ||||||
| chr22:49802408
|
A | G | 17 | a0001c0001t0004g0013a0001c0002t0001g0030a0001c0002t0001g0031others(14): Show | 17 | HG00597.hp2 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+1796T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802408 | ||||||
| chr22:49802459
|
C | A | 18 | a0001c0001t0004g0013a0001c0002t0001g0030a0001c0002t0001g0031others(15): Show | 18 | HG00597.hp2 HG01361.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1524+1745G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802459 | ||||||
| chr22:49802492
|
ATTCCCCA others(40): Show |
A | 3 | a0001c0001t0002g0064a0001c0001t0002g0079a0001c0001t0005g0151 | 3 | HG00140.hp2 HG01515.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1524+1665_1524+171 others(51): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802492 | ||||||
| chr22:49802502
|
A | G | 17 | a0001c0001t0004g0013a0001c0002t0001g0030a0001c0002t0001g0031others(14): Show | 17 | HG00597.hp2 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+1702T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802502 | ||||||
| chr22:49802507
|
A | G | 204 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(201): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1524+1697T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802507 | ||||||
| chr22:49802511
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1524+1693C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802511 | ||||||
| chr22:49802524
|
C | CCTCCACT others(181): Show |
2 | a0001c0006t0001g0050a0001c0006t0012g0241 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1524+1679_1524+168 others(192): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802524 | ||||||
| chr22:49802539
|
T | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+1665A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802539 | ||||||
| chr22:49802554
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG01891.hp1 HG02027.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1524+1650C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802554 | ||||||
| chr22:49802599
|
G | A | 19 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(16): Show | 19 | HG00438.hp1 HG01123.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.1524+1605C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802599 | ||||||
| chr22:49802673
|
C | CTCTTCCA others(181): Show |
19 | a0002c0003t0003g0010a0002c0003t0003g0222a0002c0003t0003g0223others(16): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524+1530_1524+153 others(192): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802673 | ||||||
| chr22:49802673
|
C | G | 5 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(2): Show | 5 | HG01109.hp1 HG01515.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+1531G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802673 | ||||||
| chr22:49802695
|
G | A | 100 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(97): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1524+1509C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802695 | ||||||
| chr22:49802737
|
G | A | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1524+1467C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802737 | ||||||
| chr22:49802782
|
G | A | 1 | a0002c0003t0003g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1524+1422C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802782 | ||||||
| chr22:49802836
|
G | A | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1524+1368C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802836 | ||||||
| chr22:49802948
|
G | T | 1 | a0004c0013t0001g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1524+1256C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802948 | ||||||
| chr22:49803077
|
T | C | 1 | a0001c0001t0002g0071 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1524+1127A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803077 | ||||||
| chr22:49803083
|
C | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+1121G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803083 | ||||||
| chr22:49803233
|
G | GCCACCGC others(1): Show |
3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1524+963_1524+970d others(10): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803233 | ||||||
| chr22:49803238
|
C | T | 6 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+966G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803238 | ||||||
| chr22:49803273
|
T | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+931A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803273 | ||||||
| chr22:49803392
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1524+812C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803392 | ||||||
| chr22:49803655
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+549G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803655 | ||||||
| chr22:49803667
|
C | T | 1 | a0001c0004t0001g0191 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1524+537G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803667 | ||||||
| chr22:49803679
|
T | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1524+525A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803679 | ||||||
| chr22:49803680
|
C | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1524+524G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803680 | ||||||
| chr22:49803817
|
G | A | 24 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(21): Show | 24 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1524+387C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803817 | ||||||
| chr22:49803939
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1524+265C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49803939 | ||||||
| chr22:49804012
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1524+192G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49804012 | ||||||
| chr22:49804109
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1524+95C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49804109 | ||||||
| chr22:49804406
|
T | C | 1 | a0001c0002t0002g0158 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1368-46A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804406 | ||||||
| chr22:49804429
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1368-69A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804429 | ||||||
| chr22:49804440
|
C | T | 1 | a0001c0018t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1368-80G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804440 | ||||||
| chr22:49804735
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1368-375G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804735 | ||||||
| chr22:49804752
|
G | A | 24 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0004t0001g0018others(21): Show | 25 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.1368-392C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804752 | ||||||
| chr22:49804766
|
G | A | 4 | a0001c0001t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(1): Show | 4 | HG00597.hp2 NA18612.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-406C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804766 | ||||||
| chr22:49804834
|
G | C | 112 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(109): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1368-474C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804834 | ||||||
| chr22:49804869
|
A | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-509T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49804869 | ||||||
| chr22:49805237
|
C | G | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-877G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805237 | ||||||
| chr22:49805304
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1368-944G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805304 | ||||||
| chr22:49805364
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1368-1004G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805364 | ||||||
| chr22:49805405
|
G | A | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-1045C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805405 | ||||||
| chr22:49805553
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1368-1193C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805553 | ||||||
| chr22:49805616
|
G | A | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1368-1256C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805616 | ||||||
| chr22:49805635
|
A | T | 1 | a0001c0001t0002g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1368-1275T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805635 | ||||||
| chr22:49805730
|
G | T | 113 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1368-1370C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805730 | ||||||
| chr22:49805741
|
C | CT | 9 | a0001c0001t0001g0176a0001c0001t0002g0074a0001c0001t0002g0086others(6): Show | 10 | HG01361.hp2 HG01884.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1368-1382dupA | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805741 | ||||||
| chr22:49805741
|
CT | C | 42 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 42 | HG01255.hp2 HG01256.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.1368-1382delA | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805741 | ||||||
| chr22:49805741
|
CTT | C | 23 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1368-1383_1368-138 others(6): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805741 | ||||||
| chr22:49805804
|
C | T | 4 | a0001c0001t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(1): Show | 4 | HG00597.hp2 NA18612.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-1444G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805804 | ||||||
| chr22:49805847
|
T | C | 1 | a0002c0003t0003g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1368-1487A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805847 | ||||||
| chr22:49805941
|
C | T | 113 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1368-1581G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49805941 | ||||||
| chr22:49806010
|
G | C | 1 | a0001c0018t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1368-1650C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49806010 | ||||||
| chr22:49806037
|
G | A | 1 | a0001c0006t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1368-1677C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49806037 | ||||||
| chr22:49806688
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1368-2328G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49806688 | ||||||
| chr22:49806796
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0002g0118 | 2 | HG03688.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1368-2436C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49806796 | ||||||
| chr22:49806855
|
G | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1368-2495C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49806855 | ||||||
| chr22:49806998
|
CA | C | 34 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(31): Show | 35 | HG01256.hp2 HG01516.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1368-2639delT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49806998 | ||||||
| chr22:49806998
|
CAA | C | 98 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(95): Show | 102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1368-2640_1368-263 others(6): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49806998 | ||||||
| chr22:49807117
|
A | G | 5 | a0001c0004t0001g0190a0001c0004t0001g0191a0001c0004t0001g0197others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368-2757T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49807117 | ||||||
| chr22:49807398
|
C | T | 1 | a0001c0004t0001g0189 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1368-3038G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49807398 | ||||||
| chr22:49807449
|
T | G | 25 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(22): Show | 25 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1368-3089A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49807449 | ||||||
| chr22:49807461
|
T | C | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1368-3101A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49807461 | ||||||
| chr22:49807491
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1368-3131C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49807491 | ||||||
| chr22:49807901
|
G | A | 14 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(11): Show | 14 | HG00438.hp2 HG00558.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1368-3541C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49807901 | ||||||
| chr22:49808027
|
C | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA19007.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1368-3667G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808027 | ||||||
| chr22:49808027
|
C | CA | 74 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0164others(71): Show | 77 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1368-3668dupT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808027 | ||||||
| chr22:49808080
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-3720C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808080 | ||||||
| chr22:49808104
|
C | T | 6 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-3744G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808104 | ||||||
| chr22:49808141
|
A | T | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1368-3781T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808141 | ||||||
| chr22:49808446
|
G | A | 2 | a0001c0002t0001g0003a0004c0013t0001g0209 | 4 | HG02257.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-4086C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808446 | ||||||
| chr22:49808476
|
T | C | 17 | a0001c0001t0004g0013a0001c0002t0001g0030a0001c0002t0001g0031others(14): Show | 17 | HG00597.hp2 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1368-4116A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808476 | ||||||
| chr22:49808498
|
C | T | 3 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056 | 3 | HG03209.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1368-4138G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808498 | ||||||
| chr22:49808608
|
T | C | 2 | a0001c0002t0001g0003a0004c0013t0001g0209 | 4 | HG02257.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-4248A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808608 | ||||||
| chr22:49808628
|
A | G | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1368-4268T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808628 | ||||||
| chr22:49808734
|
G | C | 1 | a0001c0001t0002g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1368-4374C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808734 | ||||||
| chr22:49808841
|
G | A | 1 | a0001c0002t0004g0016 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1368-4481C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808841 | ||||||
| chr22:49808852
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1368-4492G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49808852 | ||||||
| chr22:49809044
|
G | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1368-4684C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809044 | ||||||
| chr22:49809140
|
G | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1368-4780C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809140 | ||||||
| chr22:49809223
|
T | TTG | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-4865_1368-486 others(6): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809223 | ||||||
| chr22:49809259
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA19058.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1368-4899T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809259 | ||||||
| chr22:49809302
|
G | A | 3 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0121 | 3 | NA18969.hp1 NA19005.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1368-4942C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809302 | ||||||
| chr22:49809308
|
G | A | 27 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054others(24): Show | 28 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1368-4948C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809308 | ||||||
| chr22:49809428
|
T | A | 1 | a0001c0004t0001g0203 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1368-5068A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809428 | ||||||
| chr22:49809455
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0084 | 2 | HG00558.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1368-5095G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809455 | ||||||
| chr22:49809504
|
G | A | 9 | a0002c0003t0003g0221a0002c0003t0003g0224a0002c0003t0003g0225others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.1368-5144C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809504 | ||||||
| chr22:49809523
|
G | A | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1368-5163C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809523 | ||||||
| chr22:49809541
|
C | CA | 9 | a0001c0001t0001g0122a0001c0001t0001g0146a0001c0001t0002g0002others(6): Show | 12 | HG00642.hp1 HG01123.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-5182dupT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809541 | ||||||
| chr22:49809541
|
C | CAAA | 24 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(21): Show | 24 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1368-5184_1368-518 others(7): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809541 | ||||||
| chr22:49809548
|
A | T | 4 | a0001c0001t0002g0064a0001c0001t0002g0079a0001c0001t0002g0141others(1): Show | 4 | HG00140.hp2 HG01106.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-5188T>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809548 | ||||||
| chr22:49809549
|
AT | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1368-5190delA | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809549 | ||||||
| chr22:49809550
|
T | A | 96 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1368-5190A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809550 | ||||||
| chr22:49809552
|
T | A | 53 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1368-5192A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809552 | ||||||
| chr22:49809554
|
T | A | 21 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(18): Show | 22 | HG01433.hp1 HG01891.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.1368-5194A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809554 | ||||||
| chr22:49809556
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1368-5196A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809556 | ||||||
| chr22:49809714
|
G | A | 9 | a0001c0002t0001g0030a0001c0004t0001g0197a0001c0005t0001g0009others(6): Show | 10 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1368-5354C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809714 | ||||||
| chr22:49809738
|
T | C | 2 | a0001c0005t0001g0192a0001c0005t0001g0193 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1368-5378A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809738 | ||||||
| chr22:49809868
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0134 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1368-5508C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809868 | ||||||
| chr22:49809874
|
A | G | 6 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-5514T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809874 | ||||||
| chr22:49809941
|
T | C | 2 | a0001c0004t0001g0018a0001c0004t0001g0199 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1368-5581A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809941 | ||||||
| chr22:49810041
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1368-5681T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810041 | ||||||
| chr22:49810171
|
C | G | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG01255.hp2 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1368-5811G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810171 | ||||||
| chr22:49810360
|
A | G | 1 | a0001c0006t0001g0055 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1368-6000T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810360 | ||||||
| chr22:49810408
|
C | T | 1 | a0001c0001t0011g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1368-6048G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810408 | ||||||
| chr22:49810436
|
G | A | 1 | a0001c0004t0001g0189 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1368-6076C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810436 | ||||||
| chr22:49810625
|
A | G | 25 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(22): Show | 25 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1368-6265T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810625 | ||||||
| chr22:49810653
|
A | G | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1368-6293T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810653 | ||||||
| chr22:49810797
|
G | A | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-6437C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810797 | ||||||
| chr22:49810805
|
A | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1368-6445T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810805 | ||||||
| chr22:49810813
|
G | A | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-6453C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810813 | ||||||
| chr22:49810989
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1368-6629T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49810989 | ||||||
| chr22:49811064
|
G | A | 123 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(120): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1368-6704C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811064 | ||||||
| chr22:49811083
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1368-6723G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811083 | ||||||
| chr22:49811098
|
G | A | 8 | a0001c0004t0001g0018a0001c0004t0001g0195a0001c0004t0001g0199others(5): Show | 8 | HG01256.hp2 HG02040.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-6738C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811098 | ||||||
| chr22:49811160
|
CA | C | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1368-6801delT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811160 | ||||||
| chr22:49811264
|
T | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-6904A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811264 | ||||||
| chr22:49811271
|
A | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-6911T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811271 | ||||||
| chr22:49811312
|
T | TG | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1368-6953_1368-695 others(5): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811312 | ||||||
| chr22:49811545
|
G | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1368-7185C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811545 | ||||||
| chr22:49811595
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-7235C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811595 | ||||||
| chr22:49811600
|
G | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(4): Show | 7 | HG01255.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1368-7240C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811600 | ||||||
| chr22:49811709
|
C | T | 1 | a0001c0002t0001g0215 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1368-7349G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811709 | ||||||
| chr22:49811887
|
T | C | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-7527A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811887 | ||||||
| chr22:49811937
|
T | C | 1 | a0001c0001t0002g0007 | 2 | HG02071.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1368-7577A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49811937 | ||||||
| chr22:49812100
|
GCTC | G | 19 | a0001c0004t0001g0190a0001c0004t0001g0191a0001c0004t0001g0195others(16): Show | 20 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1368-7743_1368-774 others(7): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812100 | ||||||
| chr22:49812104
|
C | CT | 56 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0164others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1368-7745dupA | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812104 | ||||||
| chr22:49812104
|
CTTT | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG01255.hp2 HG01891.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1368-7747_1368-774 others(7): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812104 | ||||||
| chr22:49812173
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1368-7813C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812173 | ||||||
| chr22:49812255
|
G | A | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1368-7895C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812255 | ||||||
| chr22:49812435
|
G | A | 7 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(4): Show | 7 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-8075C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812435 | ||||||
| chr22:49812681
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1368-8321G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812681 | ||||||
| chr22:49812703
|
C | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1368-8343G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812703 | ||||||
| chr22:49812893
|
G | C | 1 | a0001c0001t0002g0135 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1368-8533C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812893 | ||||||
| chr22:49812925
|
G | A | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1368-8565C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49812925 | ||||||
| chr22:49813022
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1368-8662C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813022 | ||||||
| chr22:49813218
|
C | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01255.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-8858G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813218 | ||||||
| chr22:49813543
|
T | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 8 | HG00741.hp2 HG01433.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1368-9183A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813543 | ||||||
| chr22:49813652
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1368-9292G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813652 | ||||||
| chr22:49813653
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1368-9293C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813653 | ||||||
| chr22:49813695
|
G | A | 6 | a0001c0005t0001g0009a0001c0005t0001g0204a0001c0005t0001g0205others(3): Show | 7 | HG01884.hp1 HG02486.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1367+9256C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813695 | ||||||
| chr22:49813827
|
TA | T | 28 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 28 | HG01069.hp2 HG01255.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.1367+9123delT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813827 | ||||||
| chr22:49813891
|
A | G | 1 | a0001c0004t0001g0189 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1367+9060T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813891 | ||||||
| chr22:49813893
|
A | G | 3 | a0001c0001t0002g0045a0001c0001t0002g0077a0001c0001t0010g0078 | 3 | HG01496.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1367+9058T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813893 | ||||||
| chr22:49813922
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1367+9029T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813922 | ||||||
| chr22:49813969
|
G | A | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1367+8982C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49813969 | ||||||
| chr22:49814055
|
G | A | 112 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(109): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1367+8896C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814055 | ||||||
| chr22:49814081
|
A | C | 1 | a0001c0002t0001g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1367+8870T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814081 | ||||||
| chr22:49814127
|
C | T | 1 | a0002c0003t0003g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1367+8824G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814127 | ||||||
| chr22:49814153
|
G | C | 1 | a0001c0001t0002g0136 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1367+8798C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814153 | ||||||
| chr22:49814286
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1367+8665C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814286 | ||||||
| chr22:49814342
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1367+8609C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814342 | ||||||
| chr22:49814350
|
G | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(6): Show | 10 | HG00741.hp2 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367+8601C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814350 | ||||||
| chr22:49814353
|
C | T | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG01255.hp2 HG01891.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1367+8598G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814353 | ||||||
| chr22:49814371
|
C | T | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(8): Show | 12 | HG00741.hp2 HG01261.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1367+8580G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814371 | ||||||
| chr22:49814397
|
G | A | 2 | a0001c0002t0001g0003a0004c0013t0001g0209 | 4 | HG02257.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+8554C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814397 | ||||||
| chr22:49814705
|
G | A | 6 | a0001c0004t0001g0195a0001c0004t0001g0200a0001c0004t0001g0201others(3): Show | 6 | HG01256.hp2 HG02040.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+8246C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814705 | ||||||
| chr22:49814728
|
C | T | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1367+8223G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814728 | ||||||
| chr22:49814736
|
G | C | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+8215C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814736 | ||||||
| chr22:49814751
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 8 | HG00741.hp2 HG01433.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+8200C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814751 | ||||||
| chr22:49814959
|
C | T | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+7992G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814959 | ||||||
| chr22:49814973
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1367+7978C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49814973 | ||||||
| chr22:49815022
|
C | T | 1 | a0001c0004t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1367+7929G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815022 | ||||||
| chr22:49815328
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1367+7623G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815328 | ||||||
| chr22:49815333
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1367+7618T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815333 | ||||||
| chr22:49815364
|
G | A | 46 | a0001c0002t0001g0003a0001c0002t0001g0030a0001c0002t0001g0031others(43): Show | 49 | HG01256.hp2 HG01361.hp2 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.1367+7587C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815364 | ||||||
| chr22:49815404
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG00642.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+7547C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815404 | ||||||
| chr22:49815412
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1367+7539C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815412 | ||||||
| chr22:49815472
|
G | A | 25 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(22): Show | 25 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1367+7479C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815472 | ||||||
| chr22:49815551
|
GA | G | 100 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(97): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1367+7399delT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815551 | ||||||
| chr22:49815954
|
AGTGCCAC others(59): Show |
A | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | NA18939.hp1 NA18947.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+6931_1367+699 others(70): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49815954 | ||||||
| chr22:49816089
|
C | T | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1367+6862G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816089 | ||||||
| chr22:49816201
|
G | T | 1 | a0002c0003t0003g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1367+6750C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816201 | ||||||
| chr22:49816207
|
G | A | 23 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(20): Show | 24 | HG00741.hp2 HG01433.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1367+6744C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816207 | ||||||
| chr22:49816226
|
C | T | 104 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(101): Show | 108 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.1367+6725G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816226 | ||||||
| chr22:49816299
|
C | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+6652G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816299 | ||||||
| chr22:49816327
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+6624T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816327 | ||||||
| chr22:49816373
|
G | A | 2 | a0003c0007t0006g0004a0003c0007t0006g0011 | 3 | HG02559.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1367+6578C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816373 | ||||||
| chr22:49816427
|
G | A | 2 | a0002c0003t0003g0234a0002c0003t0003g0235 | 2 | HG01261.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1367+6524C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816427 | ||||||
| chr22:49816526
|
C | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+6425G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816526 | ||||||
| chr22:49816527
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+6424T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816527 | ||||||
| chr22:49816674
|
G | T | 1 | a0002c0003t0003g0222 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1367+6277C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49816674 | ||||||
| chr22:49817109
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1367+5842C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817109 | ||||||
| chr22:49817130
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+5821G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817130 | ||||||
| chr22:49817149
|
A | C | 1 | a0001c0015t0002g0149 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1367+5802T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817149 | ||||||
| chr22:49817186
|
G | T | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1367+5765C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817186 | ||||||
| chr22:49817475
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+5476G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817475 | ||||||
| chr22:49817505
|
T | C | 1 | a0002c0003t0003g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1367+5446A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817505 | ||||||
| chr22:49817549
|
G | A | 1 | a0001c0019t0001g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1367+5402C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817549 | ||||||
| chr22:49817595
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1367+5356G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817595 | ||||||
| chr22:49817619
|
C | T | 4 | a0002c0003t0003g0225a0002c0003t0003g0226a0002c0003t0003g0227others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+5332G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817619 | ||||||
| chr22:49817646
|
C | T | 23 | a0001c0008t0001g0019a0001c0018t0001g0049a0002c0003t0003g0010others(20): Show | 24 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1367+5305G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817646 | ||||||
| chr22:49817647
|
G | A | 75 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0164others(72): Show | 78 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1367+5304C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817647 | ||||||
| chr22:49817874
|
G | A | 1 | a0002c0003t0003g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1367+5077C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817874 | ||||||
| chr22:49817892
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1367+5059G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817892 | ||||||
| chr22:49817948
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG00642.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+5003T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817948 | ||||||
| chr22:49817969
|
C | T | 2 | a0002c0003t0003g0221a0002c0003t0003g0224 | 2 | HG00323.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1367+4982G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49817969 | ||||||
| chr22:49818018
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1367+4933T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818018 | ||||||
| chr22:49818042
|
G | A | 6 | a0001c0005t0001g0009a0001c0005t0001g0204a0001c0005t0001g0205others(3): Show | 7 | HG01884.hp1 HG02486.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1367+4909C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818042 | ||||||
| chr22:49818116
|
A | C | 1 | a0004c0013t0001g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1367+4835T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818116 | ||||||
| chr22:49818145
|
G | A | 1 | a0006c0014t0001g0208 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1367+4806C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818145 | ||||||
| chr22:49818241
|
G | A | 1 | a0001c0002t0001g0003 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1367+4710C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818241 | ||||||
| chr22:49818278
|
C | T | 1 | a0001c0002t0001g0216 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1367+4673G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818278 | ||||||
| chr22:49818291
|
C | G | 1 | a0001c0001t0002g0074 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1367+4660G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818291 | ||||||
| chr22:49818366
|
C | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0054 | 3 | HG02451.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1367+4585G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818366 | ||||||
| chr22:49818445
|
A | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+4506T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818445 | ||||||
| chr22:49818474
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1367+4477A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818474 | ||||||
| chr22:49818616
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01255.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+4335C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818616 | ||||||
| chr22:49818637
|
T | C | 238 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(235): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1367+4314A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818637 | ||||||
| chr22:49818711
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1367+4240G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818711 | ||||||
| chr22:49818806
|
A | C | 1 | a0001c0001t0002g0073 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1367+4145T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818806 | ||||||
| chr22:49818918
|
T | C | 21 | a0002c0003t0003g0010a0002c0003t0003g0221a0002c0003t0003g0222others(18): Show | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1367+4033A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818918 | ||||||
| chr22:49818925
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1367+4026C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49818925 | ||||||
| chr22:49819175
|
G | A | 3 | a0001c0001t0002g0064a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG00140.hp2 HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1367+3776C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819175 | ||||||
| chr22:49819192
|
G | A | 7 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(4): Show | 7 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367+3759C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819192 | ||||||
| chr22:49819195
|
G | A | 3 | a0002c0003t0003g0237a0002c0003t0003g0238a0002c0003t0003g0239 | 3 | HG02615.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1367+3756C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819195 | ||||||
| chr22:49819581
|
G | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+3370C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819581 | ||||||
| chr22:49819734
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+3217G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819734 | ||||||
| chr22:49819877
|
C | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG00642.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+3074G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819877 | ||||||
| chr22:49819904
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1367+3047A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819904 | ||||||
| chr22:49819928
|
A | G | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1367+3023T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819928 | ||||||
| chr22:49819941
|
C | T | 9 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0068others(6): Show | 9 | HG01069.hp1 HG01074.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367+3010G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819941 | ||||||
| chr22:49820034
|
G | A | 124 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(121): Show | 129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1367+2917C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820034 | ||||||
| chr22:49820143
|
GA | G | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+2807delT | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820143 | ||||||
| chr22:49820144
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1367+2807T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820144 | ||||||
| chr22:49820236
|
T | C | 1 | a0002c0003t0003g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1367+2715A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820236 | ||||||
| chr22:49820252
|
G | A | 4 | a0001c0001t0001g0143a0001c0006t0001g0055a0001c0006t0001g0056others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+2699C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820252 | ||||||
| chr22:49820284
|
G | C | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG01433.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+2667C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820284 | ||||||
| chr22:49820285
|
C | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367+2666G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820285 | ||||||
| chr22:49820373
|
G | A | 237 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(234): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1367+2578C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820373 | ||||||
| chr22:49820421
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1367+2530C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820421 | ||||||
| chr22:49820512
|
G | A | 1 | a0003c0007t0006g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1367+2439C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820512 | ||||||
| chr22:49820527
|
G | C | 30 | a0001c0001t0002g0153a0001c0002t0002g0154a0001c0002t0002g0155others(27): Show | 31 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.1367+2424C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820527 | ||||||
| chr22:49820587
|
C | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+2364G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49820587 | ||||||
| chr22:49821190
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG00741.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1367+1761G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49821190 | ||||||
| chr22:49821604
|
CTTCT | C | 20 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(17): Show | 20 | HG00438.hp1 HG01123.hp1 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.1367+1343_1367+134 others(8): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49821604 | ||||||
| chr22:49821607
|
CT | C | 106 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 111 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1367+1343delA | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49821607 | ||||||
| chr22:49821901
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+1050C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49821901 | ||||||
| chr22:49821954
|
G | A | 2 | a0002c0003t0003g0234a0002c0003t0003g0235 | 2 | HG01261.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1367+997C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49821954 | ||||||
| chr22:49822339
|
T | G | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1367+612A>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822339 | ||||||
| chr22:49822454
|
T | C | 2 | a0001c0002t0002g0158a0005c0012t0002g0159 | 2 | NA18957.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1367+497A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822454 | ||||||
| chr22:49822480
|
G | A | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1367+471C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822480 | ||||||
| chr22:49822578
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1367+373G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822578 | ||||||
| chr22:49822583
|
G | A | 25 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(22): Show | 25 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1367+368C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822583 | ||||||
| chr22:49822642
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1367+309C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822642 | ||||||
| chr22:49822644
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0002g0147 | 2 | NA18986.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1367+307C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822644 | ||||||
| chr22:49822656
|
G | C | 2 | a0002c0003t0003g0234a0002c0003t0003g0235 | 2 | HG01261.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1367+295C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822656 | ||||||
| chr22:49822688
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1367+263G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49822688 | ||||||
| chr22:49824491
|
C | T | 23 | a0001c0004t0001g0018a0001c0004t0001g0189a0001c0004t0001g0190others(20): Show | 24 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-14-160G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824491 | ||||||
| chr22:49824528
|
A | C | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-197T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824528 | ||||||
| chr22:49824651
|
G | C | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14-320C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824651 | ||||||
| chr22:49824768
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-437C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824768 | ||||||
| chr22:49824811
|
C | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG01255.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-14-480G>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824811 | ||||||
| chr22:49824940
|
T | C | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-14-609A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824940 | ||||||
| chr22:49824944
|
C | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-14-613G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824944 | ||||||
| chr22:49824963
|
A | C | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-14-632T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49824963 | ||||||
| chr22:49825155
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0005g0150a0001c0001t0005g0151 | 4 | NA18966.hp1 NA18995.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-824C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825155 | ||||||
| chr22:49825332
|
G | A | 3 | a0001c0001t0011g0152a0003c0007t0006g0004a0003c0007t0006g0011 | 4 | HG00741.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1001C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825332 | ||||||
| chr22:49825471
|
C | T | 31 | a0001c0002t0001g0003a0001c0002t0001g0051a0001c0002t0001g0052others(28): Show | 34 | HG01256.hp2 HG01884.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14-1140G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825471 | ||||||
| chr22:49825538
|
G | A | 8 | a0001c0001t0002g0153a0001c0002t0002g0154a0001c0002t0002g0155others(5): Show | 8 | HG02155.hp2 NA18612.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-1207C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825538 | ||||||
| chr22:49825685
|
G | A | 6 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-1354C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825685 | ||||||
| chr22:49825703
|
G | A | 24 | a0001c0006t0001g0050a0001c0006t0012g0241a0001c0018t0001g0049others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14-1372C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825703 | ||||||
| chr22:49825846
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-14-1515C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825846 | ||||||
| chr22:49825954
|
C | T | 1 | a0001c0008t0001g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15+1543G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49825954 | ||||||
| chr22:49826087
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+1410A>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826087 | ||||||
| chr22:49826304
|
C | T | 22 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.-15+1193G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826304 | ||||||
| chr22:49826477
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | NA18939.hp1 NA18947.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+1020C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826477 | ||||||
| chr22:49826499
|
G | A | 3 | a0001c0001t0007g0211a0001c0001t0007g0212a0001c0001t0007g0213 | 3 | HG02622.hp2 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-15+998C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826499 | ||||||
| chr22:49826539
|
C | T | 3 | a0001c0001t0007g0211a0001c0001t0007g0212a0001c0001t0007g0213 | 3 | HG02622.hp2 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-15+958G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826539 | ||||||
| chr22:49826656
|
CTGTGCGA others(5): Show |
C | 5 | a0001c0004t0001g0189a0001c0004t0001g0190a0001c0004t0001g0191others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+829_-15+840del others(12): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826656 | ||||||
| chr22:49826687
|
C | A | 1 | a0002c0003t0003g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15+810G>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826687 | ||||||
| chr22:49826736
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-15+761G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826736 | ||||||
| chr22:49826801
|
G | T | 1 | a0001c0001t0002g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+696C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826801 | ||||||
| chr22:49826822
|
G | C | 6 | a0001c0002t0001g0214a0001c0002t0001g0215a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp1 HG03017.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+675C>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826822 | ||||||
| chr22:49826834
|
G | A | 24 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(21): Show | 24 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-15+663C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826834 | ||||||
| chr22:49826907
|
A | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0186others(3): Show | 6 | HG01255.hp2 HG02886.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+590T>G | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49826907 | ||||||
| chr22:49827108
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG01255.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+389C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827108 | ||||||
| chr22:49827149
|
G | A | 5 | a0001c0004t0001g0189a0001c0004t0001g0190a0001c0004t0001g0191others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+348C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827149 | ||||||
| chr22:49827290
|
G | GGCCCGAC others(15): Show |
1 | a0001c0006t0012g0241 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-15+185_-15+206dup others(22): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827290 | ||||||
| chr22:49827360
|
A | AGCCGCC | 50 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(47): Show | 53 | HG00597.hp2 HG01256.hp2 HG01361.hp2 others(50): Show |
intron_variant | MODIFIER | c.-15+131_-15+136dup others(6): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827360 | ||||||
| chr22:49827360
|
A | AGCCGCCG others(5): Show |
1 | a0001c0004t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15+125_-15+136dup others(12): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827360 | ||||||
| chr22:49827360
|
A | AGCCGCCG others(8): Show |
2 | a0001c0002t0001g0214a0001c0002t0001g0215 | 2 | NA18940.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-15+122_-15+136dup others(15): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827360 | ||||||
| chr22:49827360
|
A | G | 1 | a0001c0001t0002g0017 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15+137T>C | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827360 | ||||||
| chr22:49827360
|
AGCC | A | 5 | a0001c0001t0007g0211a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+134_-15+136del others(3): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827360 | ||||||
| chr22:49827360
|
AGCCGCCG others(5): Show |
A | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+125_-15+136del others(12): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827360 | ||||||
| chr22:49827413
|
G | GAGGCC | 20 | a0001c0001t0007g0211a0001c0001t0007g0212a0001c0001t0007g0213others(17): Show | 21 | HG01256.hp2 HG01884.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+79_-15+83dupGG others(3): Show |
BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827413 | ||||||
| chr22:49827466
|
G | A | 8 | a0001c0002t0001g0003a0001c0002t0001g0214a0001c0002t0001g0215others(5): Show | 10 | HG02040.hp1 HG02257.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+31C>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 1/12 | chr22 | 49827466 |