Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MRRKG others(1184): Show |
chr22 | 49768283 | 49832873 |
| a0002 | 0/0 | 1189 | 22 | 10 | 3 | 0 | 4 | 5 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | MRRKG others(1184): Show |
chr22 | 49768283 | 49832873 |
| a0003 | 0/0 | 1189 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | MRRKG others(1184): Show |
chr22 | 49768283 | 49832873 |
| a0004 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | MRRKG others(1184): Show |
chr22 | 49768283 | 49832873 |
| a0005 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | MRRKG others(1184): Show |
chr22 | 49768283 | 49832873 |
| a0006 | 0/0 | 1189 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | MRRKG others(1184): Show |
chr22 | 49768283 | 49832873 |
| a0007 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | MRRKG others(1184): Show |
chr22 | 49768283 | 49832873 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3567 | 161 | 36 | 27 | 69 | 8 | 19 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0002 | 0/0 | 3567 | 34 | 10 | 1 | 19 | 0 | 4 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0004 | 0/0 | 3567 | 12 | 8 | 1 | 2 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0005 | 0/0 | 3567 | 10 | 10 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0006 | 0/0 | 3567 | 5 | 3 | 0 | 0 | 0 | 2 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0008 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0009 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0010 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0015 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0016 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0018 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0001c0019 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0002c0003 | 0/0 | 3567 | 21 | 9 | 3 | 0 | 4 | 5 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0002c0017 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0003c0007 | 0/0 | 3567 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0004c0014 | 0/0 | 3567 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0005c0013 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0006c0011 | 0/0 | 3567 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 | ||
| a0007c0012 | 0/0 | 3567 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | ATGAG others(3562): Show |
chr22 | 49768283 | 49832873 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4911 | 63 | 16 | 8 | 27 | 1 | 11 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0001t0002 | 1/1 | 4911 | 88 | 17 | 18 | 36 | 7 | 8 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0001t0004 | 0/0 | 4917 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4912): Show |
chr22 | 49768283 | 49832873 |
| a0001c0001t0005 | 0/0 | 4911 | 4 | 0 | 0 | 4 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0001t0007 | 0/0 | 4911 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0001t0009 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0001t0010 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0002t0001 | 0/0 | 4911 | 25 | 10 | 1 | 10 | 0 | 4 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0002t0002 | 0/0 | 4911 | 5 | 0 | 0 | 5 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0002t0004 | 0/0 | 4917 | 3 | 0 | 0 | 3 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4912): Show |
chr22 | 49768283 | 49832873 |
| a0001c0002t0008 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0004t0001 | 0/0 | 4911 | 12 | 8 | 1 | 2 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0005t0001 | 0/0 | 4911 | 10 | 10 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0006t0001 | 0/0 | 4911 | 4 | 3 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0006t0011 | 0/0 | 4911 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0008t0001 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0009t0002 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0010t0002 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0015t0002 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0016t0002 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0018t0001 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0001c0019t0001 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0002c0003t0003 | 0/0 | 4911 | 21 | 9 | 3 | 0 | 4 | 5 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0002c0017t0003 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0003c0007t0006 | 0/0 | 4899 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4894): Show |
chr22 | 49768283 | 49832873 |
| a0004c0014t0001 | 0/0 | 4911 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0005c0013t0001 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0006c0011t0001 | 0/0 | 4911 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
chr22 | 49768283 | 49832873 |
| a0007c0012t0002 | 0/0 | 4911 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | GCATT others(4906): Show |
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 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0093 | 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 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0001g0193 | 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 |
| a0001c0001t0002g0003 | 1/0 | 3 | 1 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0008 | 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 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0085 | 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 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0094 | 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 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0128 | 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 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0002g0161 | 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 |
| a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0001t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0004 | 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 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| 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 |
| a0001c0004t0001g0188 | 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 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0191 | 0/0 | 1 | 1 | 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 |
| a0001c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0005t0001g0203 | 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 |
| a0001c0005t0001g0209 | 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 |
| a0001c0006t0011g0239 | 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 |
| a0001c0009t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0010t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0015t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0001c0016t0002g0159 | 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 |
| a0002c0003t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0002c0017t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0003c0007t0006g0006 | 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 |
| a0004c0014t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0005c0013t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0006c0011t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| a0007c0012t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0003 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00099 | hp2 | a0002 | c0003 | t0003 | g0224 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00140 | hp1 | a0002 | c0003 | t0003 | g0222 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0140 | EUR | GBR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00323 | hp1 | a0002 | c0003 | t0003 | g0220 | EUR | FIN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | FIN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0100 | 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 | g0162 | 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 | g0163 | EAS | CHS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0114 | 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 | t0001 | g0151 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01074 | hp1 | a0002 | c0003 | t0003 | g0223 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01074 | hp2 | a0001 | c0015 | t0002 | g0148 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0231 | 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 | g0066 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0134 | 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 | g0186 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0199 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01261 | hp2 | a0002 | c0003 | t0003 | g0234 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0141 | 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 | g0065 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01496 | hp1 | a0001 | c0010 | t0002 | g0106 | AMR | CLM | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0076 | 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 | g0077 | EUR | IBS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0063 | EUR | IBS | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0204 | 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 | g0005 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0194 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0091 | 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 | g0008 | 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 | g0122 | EAS | KHV | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0164 | 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 | g0117 | EAS | CDX | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | CDX | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0197 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02300 | hp1 | a0004 | c0014 | t0001 | g0207 | AMR | PEL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0131 | 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 | a0005 | c0013 | t0001 | g0208 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02602 | hp1 | a0002 | c0003 | t0003 | g0230 | 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 | g0235 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0192 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02622 | hp1 | a0002 | c0003 | t0003 | g0228 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0212 | 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 | g0178 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0103 | 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 | g0233 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0160 | 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 | g0210 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0196 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0193 | 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 | g0004 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0004 | 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 | g0195 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0010 | 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 | g0211 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0109 | 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 | g0074 | 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 | g0115 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0198 | 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 | g0203 | 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 | g0238 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0179 | 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 | g0137 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0226 | 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 | g0236 | AFR | ESN | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0200 | AFR | GWD | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | 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 | a0006 | c0011 | t0001 | g0180 | 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 | g0201 | 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 | t0011 | g0239 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03710 | hp2 | a0002 | c0003 | t0003 | g0227 | SAS | PJL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0092 | 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 | g0105 | SAS | BEB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | 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 | g0068 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0232 | SAS | STU | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0120 | 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 | g0006 | 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 | g0152 | EAS | CHB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0191 | 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 | g0182 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0215 | 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 | g0161 | 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 | g0157 | 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 | g0078 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0172 | 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 | g0125 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18969 | hp2 | a0001 | c0016 | t0002 | g0159 | 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 | g0111 | 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 | g0183 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0150 | 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 | g0153 | 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 | g0124 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0110 | 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 | g0086 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0005 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | LWK | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0107 | 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 | g0119 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19058 | hp2 | a0007 | c0012 | t0002 | g0158 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0126 | 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 | g0133 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0080 | 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 | g0083 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19088 | hp1 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0205 | 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 | g0185 | 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 | g0007 | EUR | TSI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0067 | EUR | TSI | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | GIH | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | 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 | g0209 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0005 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02559 | hp1 | a0001 | c0009 | t0002 | g0064 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG02559 | hp2 | a0003 | c0007 | t0006 | g0006 | AFR | ACB | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0189 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG03471 | hp2 | a0002 | c0017 | t0003 | g0229 | AFR | MSL | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| HG06807 | hp1 | a0002 | c0003 | t0003 | g0237 | 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 | g0130 | 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 | a0001 | c0001 | t0002 | g0070 | REF | REF | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | BRD1_chr22_49768283_49832873 | BRD1 | chr22 | 49768283 | 49832873 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49777735 | C | A | 1 | a0005 | 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 | a0007 | 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 | a0004 | 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 | a0006 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49774254 | G | A | 1 | a0005c0013 | 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 | a0001c0004 a0001c0005 a0004c0014 others(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 | a0001c0002 a0001c0004 a0001c0005 others(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 | a0001c0006 a0001c0018 a0002c0003 others(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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(17): 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 | a0001c0006t0011 | 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 | a0001c0001t0001 | 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 | a0001c0001t0004 a0001c0002t0004 |
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 | a0001c0006t0011 a0002c0003t0003 a0002c0017t0003 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49774478 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0003c0007t0006g0006 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0216 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0002c0003t0003g0232 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0003c0007t0006g0006 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0004c0014t0001g0207 | 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 | 134 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(131): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0151 | 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 | a0001c0004t0001g0189 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0005g0150 | 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 | a0001c0001t0002g0080 a0001c0001t0002g0113 a0001c0002t0001g0032 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0146 a0001c0001t0002g0161 others(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 | a0002c0017t0003g0229 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0169 a0001c0001t0001g0175 others(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 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0019t0001g0039 |
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 | a0001c0001t0001g0089 | 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 | a0001c0002t0001g0218 | 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 | a0001c0005t0001g0205 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0002g0136 | 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 | a0001c0004t0001g0198 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0179 a0001c0001t0007g0210 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0178 others(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 | a0001c0005t0001g0192 | 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 | a0001c0004t0001g0200 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0165 | 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 | a0001c0002t0001g0215 | 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 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
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 | a0001c0001t0002g0116 a0001c0001t0005g0009 a0001c0001t0005g0149 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0162 others(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 | a0001c0002t0001g0004 | 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 | a0001c0001t0002g0067 a0001c0008t0001g0019 a0002c0003t0003g0005 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0043 a0001c0004t0001g0195 a0001c0018t0001g0049 others(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 | a0001c0001t0001g0187 a0001c0005t0001g0192 a0006c0011t0001g0180 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0173 a0002c0003t0003g0222 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0048 others(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 | a0001c0002t0001g0004 | 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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0002t0001g0004 | 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 | 45 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(42): 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 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0178 others(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 | a0001c0001t0002g0139 | 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0193 a0001c0001t0002g0067 a0001c0001t0002g0101 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0083 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0006t0011g0239 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0002g0087 | 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 | a0001c0001t0001g0147 | 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 | 1 | a0002c0003t0003g0005 | 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 | a0001c0001t0001g0162 a0006c0011t0001g0180 |
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 | a0002c0003t0003g0226 a0002c0003t0003g0230 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | 127 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(124): 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 | a0001c0001t0002g0045 a0001c0001t0002g0075 a0001c0001t0010g0076 others(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 | a0001c0004t0001g0188 a0001c0004t0001g0190 |
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 | a0001c0001t0002g0087 | 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 | 21 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0002c0003t0003g0005 others(18): 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0001t0002g0069 | 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 | a0001c0004t0001g0196 a0001c0005t0001g0010 a0001c0005t0001g0197 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | 22 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(19): 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | 27 | a0001c0001t0001g0142 a0001c0006t0001g0050 a0001c0006t0001g0055 others(24): 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 | a0001c0005t0001g0205 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0005c0013t0001g0208 | 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 | 77 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(74): 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0007g0212 | 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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0151 | 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 | a0001c0004t0001g0195 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0002c0003t0003g0230 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0009g0095 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0160 | 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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0002g0152 a0001c0002t0002g0153 a0001c0002t0002g0154 others(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 | a0001c0004t0001g0196 a0001c0005t0001g0010 a0001c0005t0001g0197 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0216 others(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 | a0001c0001t0002g0072 | 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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 52 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(49): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0117 a0001c0001t0002g0121 |
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 | a0001c0001t0002g0045 a0001c0001t0002g0075 a0001c0001t0010g0076 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0004t0001g0194 a0001c0004t0001g0202 |
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 | a0001c0002t0002g0154 a0001c0002t0002g0155 a0001c0016t0002g0159 |
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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0002t0001g0218 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0213 a0001c0002t0001g0214 others(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 | a0001c0002t0002g0157 a0007c0012t0002g0158 |
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 | a0001c0001t0002g0143 | 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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0005t0001g0209 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 |
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 | 75 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(72): 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 | a0001c0001t0002g0117 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0002c0003t0003g0233 a0002c0003t0003g0234 |
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 | a0001c0005t0001g0010 a0001c0005t0001g0203 a0001c0005t0001g0206 |
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 | a0001c0004t0001g0199 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0162 | 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 | a0002c0003t0003g0220 a0002c0003t0003g0221 a0002c0003t0003g0222 others(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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0089 a0001c0002t0001g0030 a0001c0002t0001g0031 others(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 | a0001c0001t0002g0079 a0001c0001t0002g0132 |
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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0002g0124 | 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0151 | 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0004t0001g0195 | 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 | 22 | a0001c0008t0001g0019 a0001c0019t0001g0039 a0002c0003t0003g0005 others(19): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0002g0090 a0001c0001t0002g0108 a0001c0001t0002g0109 |
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 | a0001c0001t0001g0089 a0001c0002t0001g0004 a0001c0002t0001g0030 others(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 | a0001c0001t0002g0161 | 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 | 25 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0006t0001g0050 others(22): 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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0002g0094 | 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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0002g0109 | 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 | a0001c0004t0001g0199 | 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 | 132 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(129): 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 | a0001c0006t0001g0050 a0001c0006t0011g0239 |
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 | a0002c0003t0003g0236 | 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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0075 a0001c0001t0010g0076 |
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 | a0001c0004t0001g0200 | 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 | a0001c0001t0002g0123 | 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 | a0001c0002t0001g0216 | 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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0001g0004 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0002g0160 | 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 | 28 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0151 others(25): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0002t0001g0213 others(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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0002c0003t0003g0233 a0002c0003t0003g0234 |
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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0005t0001g0192 | 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 | a0001c0002t0001g0215 | 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 | 61 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(58): 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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | 81 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(78): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | 132 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(129): 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0088 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0042 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0025 |
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 | 39 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0151 others(36): 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 | a0001c0001t0001g0048 a0001c0001t0001g0089 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0053 others(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 | 33 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0151 others(30): 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 | a0001c0001t0001g0089 a0001c0002t0001g0037 |
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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | |||||||
| chr22:49787357 | AG | A | 5 | a0001c0001t0002g0074 a0001c0001t0002g0090 a0001c0001t0002g0103 others(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 | a0001c0001t0005g0150 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0002t0001g0004 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): 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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0002g0085 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0004t0001g0196 a0001c0005t0001g0010 a0001c0005t0001g0197 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0002c0003t0003g0222 a0002c0003t0003g0223 a0002c0003t0003g0224 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0002g0121 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0134 | 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | 121 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(118): 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 | a0001c0001t0001g0166 a0001c0001t0001g0174 |
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 | 19 | a0001c0002t0001g0004 a0001c0004t0001g0195 a0002c0003t0003g0005 others(16): 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 | a0002c0003t0003g0235 | 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 | 20 | a0002c0003t0003g0005 a0002c0003t0003g0220 a0002c0003t0003g0221 others(17): 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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0002g0090 a0001c0001t0002g0108 a0001c0001t0002g0109 |
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 | a0001c0004t0001g0188 a0001c0004t0001g0190 |
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 | a0001c0001t0010g0076 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 30 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(27): 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 | a0001c0001t0001g0089 | 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 | 121 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(118): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0001t0002g0161 | 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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0004t0001g0199 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0002c0003t0003g0226 a0002c0003t0003g0230 |
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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0089 a0001c0001t0001g0142 a0001c0001t0001g0162 others(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 | a0001c0001t0002g0063 a0001c0001t0002g0069 a0001c0009t0002g0064 |
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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0001t0002g0078 | 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 | 118 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(115): 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 | a0001c0001t0001g0089 a0001c0001t0004g0013 a0001c0002t0001g0030 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): 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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0002g0001 a0001c0001t0002g0115 |
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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0002g0134 | 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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0010t0002g0106 | 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 | a0005c0013t0001g0208 | 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 | a0001c0001t0007g0210 | 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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0151 | 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 | a0001c0006t0001g0050 a0001c0006t0011g0239 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0002g0084 | 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 | 126 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(123): 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 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
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 | 30 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(27): 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 | a0001c0001t0002g0131 | 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 | 132 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(129): 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 | 5 | a0002c0003t0003g0005 a0002c0003t0003g0235 a0002c0003t0003g0236 others(2): 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 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0004t0001g0196 a0001c0005t0001g0197 |
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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0005t0001g0010 a0001c0005t0001g0203 a0001c0005t0001g0204 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0002c0003t0003g0233 | 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 | a0001c0001t0001g0089 a0001c0001t0004g0013 a0001c0002t0001g0004 others(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 | a0001c0002t0001g0004 a0005c0013t0001g0208 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
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 | a0001c0001t0002g0065 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0002g0126 | 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 | 149 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(146): 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 | a0001c0002t0001g0004 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0005t0001g0191 a0001c0005t0001g0192 |
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 | 22 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(19): 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 | a0001c0001t0002g0123 | 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 | a0001c0004t0001g0018 a0001c0004t0001g0198 |
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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0004t0001g0195 | 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 | a0001c0001t0002g0063 a0001c0001t0002g0069 a0001c0009t0002g0064 |
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 | a0001c0004t0001g0195 | 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 | a0001c0004t0001g0200 | 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 | a0001c0002t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1525-1702A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49800821 | |||||||
| 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 41 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(38): 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0004g0013 a0001c0002t0001g0030 a0001c0002t0001g0033 others(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 | a0001c0001t0002g0115 a0001c0001t0004g0013 a0001c0002t0001g0030 others(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 | a0001c0001t0001g0142 a0001c0002t0001g0051 a0001c0002t0001g0052 others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0048 |
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 | a0001c0002t0001g0218 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0047 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0002t0001g0004 | 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 | 22 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(19): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0002t0001g0218 | 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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | 21 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0002c0003t0003g0005 others(18): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | 20 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0002c0003t0003g0005 others(17): 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 | a0001c0001t0004g0013 a0001c0002t0001g0030 a0001c0002t0001g0031 others(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 | a0001c0001t0004g0013 a0001c0002t0001g0030 a0001c0002t0001g0031 others(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 | a0001c0001t0002g0077 a0001c0001t0002g0140 a0001c0001t0005g0150 |
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 | a0001c0001t0004g0013 a0001c0002t0001g0030 a0001c0002t0001g0031 others(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 | 202 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(199): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): 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 | a0001c0001t0002g0131 | 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 | a0001c0006t0001g0050 a0001c0006t0011g0239 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 |
18 | a0002c0003t0003g0005 a0002c0003t0003g0220 a0002c0003t0003g0222 others(15): 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 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(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 | 99 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(96): 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 | a0001c0002t0001g0004 | 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 | a0002c0003t0003g0230 | 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 | a0001c0002t0001g0004 | 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 | a0005c0013t0001g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1524+1256C>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 3/12 | chr22 | 49802948 | |||||||
| chr22:49803083 | C | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0002g0069 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0004t0001g0189 | 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0162 | 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 | a0001c0002t0002g0157 | 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 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
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 | a0001c0001t0002g0087 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0004t0001g0018 others(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 | a0001c0001t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0015 others(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 | 111 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(108): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
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 | a0001c0001t0002g0086 | 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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0002t0001g0004 | 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 | a0001c0001t0002g0123 | 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 | 112 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(109): 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 | a0001c0001t0001g0176 a0001c0001t0002g0072 a0001c0001t0002g0084 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 22 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(19): 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 | a0001c0001t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0015 others(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 | a0002c0003t0003g0237 | 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 | 112 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(109): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0053 a0001c0001t0002g0123 |
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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | 97 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(94): 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 | a0001c0004t0001g0189 a0001c0004t0001g0190 a0001c0004t0001g0196 others(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 | a0001c0004t0001g0188 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0002t0001g0004 a0005c0013t0001g0208 |
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 | a0001c0001t0004g0013 a0001c0002t0001g0030 a0001c0002t0001g0031 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 |
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 | a0001c0002t0001g0004 a0005c0013t0001g0208 |
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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
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 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
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 | 26 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 others(23): 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 | a0001c0004t0001g0202 | 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 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
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 | a0002c0003t0003g0220 a0002c0003t0003g0221 a0002c0003t0003g0222 others(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 | a0001c0002t0001g0004 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0002g0002 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0002g0077 a0001c0001t0002g0139 a0001c0001t0002g0140 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0043 others(91): Show |
99 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1368-5190A>T | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49809550 | |||||||
| chr22:49809552 | T | A | 52 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(49): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0002t0001g0030 a0001c0004t0001g0196 a0001c0005t0001g0010 others(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 | a0001c0005t0001g0191 a0001c0005t0001g0192 |
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 | a0001c0001t0002g0079 a0001c0001t0002g0132 |
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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0004t0001g0018 a0001c0004t0001g0198 |
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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0151 | 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 | a0001c0004t0001g0188 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0001t0002g0080 | 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 | 122 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(119): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0004t0001g0018 a0001c0004t0001g0194 a0001c0004t0001g0198 others(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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0002t0001g0214 | 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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0001t0002g0008 | 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 | a0001c0004t0001g0189 a0001c0004t0001g0190 a0001c0004t0001g0194 others(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 | 55 | a0001c0001t0001g0142 a0001c0001t0001g0162 a0001c0001t0001g0163 others(52): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): 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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0133 | 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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0166 | 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 | a0001c0005t0001g0010 a0001c0005t0001g0203 a0001c0005t0001g0204 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0004t0001g0188 | 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 | a0001c0001t0002g0045 a0001c0001t0002g0075 a0001c0001t0010g0076 |
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 | a0001c0001t0002g0074 | 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 | a0001c0002t0001g0004 | 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 | 111 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(108): 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 | a0002c0003t0003g0220 | 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 | a0001c0001t0002g0134 | 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 | a0001c0001t0002g0135 | 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 | a0001c0001t0002g0160 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0046 others(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 | a0001c0002t0001g0004 a0005c0013t0001g0208 |
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 | a0001c0004t0001g0194 a0001c0004t0001g0199 a0001c0004t0001g0200 others(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 | a0001c0002t0001g0004 | 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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
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 | a0001c0004t0001g0194 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0073 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0030 a0001c0002t0001g0031 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | 99 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(96): 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 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): 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 | a0002c0003t0003g0220 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0002c0003t0003g0233 a0002c0003t0003g0234 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0002c0003t0003g0226 | 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0015t0002g0148 | 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0002c0003t0003g0238 | 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 | a0001c0002t0001g0219 | 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 | a0002c0003t0003g0222 a0002c0003t0003g0223 a0002c0003t0003g0224 others(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 | 22 | a0001c0008t0001g0019 a0001c0018t0001g0049 a0002c0003t0003g0005 others(19): 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 | a0001c0001t0001g0142 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0002c0003t0003g0238 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0002c0003t0003g0220 a0002c0003t0003g0221 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0005t0001g0010 a0001c0005t0001g0203 a0001c0005t0001g0204 others(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 | a0005c0013t0001g0208 | 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 | a0004c0014t0001g0207 | 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 | a0001c0002t0001g0004 | 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 | a0001c0002t0001g0215 | 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 | a0001c0001t0002g0072 | 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 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0054 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0137 | 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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | 236 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(233): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): 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 | a0001c0001t0002g0071 | 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 | 20 | a0002c0003t0003g0005 a0002c0003t0003g0220 a0002c0003t0003g0221 others(17): 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 | a0001c0001t0002g0138 | 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 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0002g0141 |
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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0002c0003t0003g0235 a0002c0003t0003g0236 a0002c0003t0003g0237 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): 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 | 8 | a0001c0001t0002g0063 a0001c0001t0002g0065 a0001c0001t0002g0066 others(5): Show |
8 | HG01069.hp1 HG01074.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+3010G>A | BRD1 | ENSG00000100425.19 | transcript | ENST00000404760.6 | protein_coding | 2/12 | chr22 | 49819941 | |||||||
| chr22:49820034 | G | A | 123 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(120): 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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0001t0002g0140 | 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 | a0002c0003t0003g0238 | 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 | a0001c0001t0001g0142 a0001c0006t0001g0055 a0001c0006t0001g0056 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(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 | 235 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(232): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): 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 | a0001c0001t0002g0143 | 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 | a0001c0001t0002g0152 a0001c0002t0002g0153 a0001c0002t0002g0154 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | 105 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(102): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0002c0003t0003g0233 a0002c0003t0003g0234 |
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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0002t0002g0157 a0007c0012t0002g0158 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0145 a0001c0001t0002g0146 |
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 | a0002c0003t0003g0233 a0002c0003t0003g0234 |
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 | a0001c0001t0001g0147 | 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 | a0001c0004t0001g0018 a0001c0004t0001g0188 a0001c0004t0001g0189 others(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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
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 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): 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 | a0001c0001t0005g0009 a0001c0001t0005g0149 a0001c0001t0005g0150 |
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 | a0001c0001t0001g0151 a0003c0007t0006g0006 a0003c0007t0006g0011 |
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 | a0001c0002t0001g0004 a0001c0002t0001g0051 a0001c0002t0001g0052 others(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 | a0001c0001t0002g0152 a0001c0002t0002g0153 a0001c0002t0002g0154 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | 23 | a0001c0006t0001g0050 a0001c0006t0011g0239 a0001c0018t0001g0049 others(20): 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 | a0001c0001t0002g0160 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(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 | a0001c0001t0007g0210 a0001c0001t0007g0211 a0001c0001t0007g0212 |
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 | a0001c0001t0007g0210 a0001c0001t0007g0211 a0001c0001t0007g0212 |
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 | a0001c0004t0001g0188 a0001c0004t0001g0189 a0001c0004t0001g0190 others(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 | a0002c0003t0003g0238 | 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 | a0001c0002t0001g0213 | 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 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0215 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0004t0001g0188 a0001c0004t0001g0189 a0001c0004t0001g0190 others(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 | a0001c0006t0011g0239 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
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 | a0001c0001t0007g0210 a0001c0001t0007g0211 a0001c0001t0007g0212 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0007g0210 a0001c0001t0007g0211 a0001c0001t0007g0212 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0213 a0001c0002t0001g0214 others(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 |